diff --git a/.github/workflows/generate-databases.yml b/.github/workflows/generate-databases.yml
new file mode 100644
index 00000000..2552523b
--- /dev/null
+++ b/.github/workflows/generate-databases.yml
@@ -0,0 +1,49 @@
+name: Generate databases
+
+on:
+  workflow_dispatch:
+  schedule:
+    - cron: "7 4 1 * *"
+  push:
+    branches: ["release", "main"]
+
+permissions:
+  contents: write
+  pull-requests: write
+
+env:
+  CARGO_TERM_COLOR: always
+  CARGO_ENCODED_RUSTFLAGS: --cfg=github_action
+
+jobs:
+  generate-databases:
+    runs-on: ubuntu-latest
+    steps:
+      - uses: actions/checkout@v4
+      - name: Check
+        run: cargo check
+      - name: Download and build external databases
+        run: |
+          bash ./.github/workflows/scripts/update-all-databases.sh
+          MESSAGE="$(cat /tmp/MESSAGES)"
+          echo "MESSAGE=${MESSAGE}" >> "${GITHUB_ENV}"
+      - name: Create pull request
+        id: cpr
+        uses: peter-evans/create-pull-request@v7
+        with:
+          token: ${{ secrets.RUSTEOMICS_MZCORE_PR_TOKEN }}
+          commit-message: Update external databases and ontologies
+          committer: GitHub <noreply@github.com>
+          author: GitHub <noreply@github.com>
+          branch: update-databases
+          delete-branch: true
+          title: "Update external databases and ontologies"
+          body: |
+            This automated PR updates the binary blobs for external databases
+            and ontologies.
+
+            Below are messages from script execution:
+              > ${{ env.MESSAGE }}
+          labels: |
+            A-rustyms-generate-databases
+            C-maintenance
diff --git a/.github/workflows/scripts/update-all-databases.sh b/.github/workflows/scripts/update-all-databases.sh
new file mode 100644
index 00000000..06e6dbd3
--- /dev/null
+++ b/.github/workflows/scripts/update-all-databases.sh
@@ -0,0 +1,76 @@
+#!/usr/bin/env bash
+
+
+function help {
+    echo "Usage: generate-all-databases.sh"
+    echo ""
+    echo "Download the required databases and build the "
+    echo "required binary representations of the ontologies."
+    echo ""
+    echo "Options:"
+    echo "  -h, --help     Display this help and exit"
+    exit 1
+}
+
+
+# Download IMGT and process and serialize it to a binary blob.
+function make-imgt {
+    echo "Downloading IMGT..."
+    mkdir -p rustyms-generate-imgt/data
+    # IMGT is not very reliable, so sometimes the server is down.
+    # The || clause here allows the rest of the script to continue
+    # even if this fails.
+    curl https://www.imgt.org/download/LIGM-DB/imgt.dat.Z \
+        | gunzip -c > rustyms-generate-imgt/data/imgt.dat \
+        && echo "Serializing IMGT ..." \
+        && cargo run --bin rustyms-generate-imgt \
+        || echo "Failed to download IMGT. I did not update it." >> /tmp/MESSAGES
+}
+
+
+# Download the relevant ontologies and serialize them to binary blobs.
+function make-ontologies {
+    echo "Downloading databases..."
+    db_data="rustyms-generate-databases/data"
+    mkdir -p ${db_data}
+    curl https://raw.githubusercontent.com/HUPO-PSI/psi-mod-CV/refs/heads/master/PSI-MOD-newstyle.obo \
+        > ${db_data}/PSI-MOD-newstyle.obo
+    curl http://www.unimod.org/obo/unimod.obo > ${db_data}/unimod.obo
+    curl ftp://ftp.proteininformationresource.org/pir_databases/other_databases/resid/RESIDUES.XML \
+        > ${db_data}/RESID-RESIDUES.XML
+    curl https://raw.githubusercontent.com/HUPO-PSI/mzIdentML/master/cv/XLMOD.obo \
+        > ${db_data}/XLMOD.obo
+    curl -L http://purl.obolibrary.org/obo/gno.obo \
+        | sed '/(property_value: GNO:00000(022|023|041|042|101|102) .*$\n)|(def: .*$\n)/d' \
+        | gzip -c \
+        > ${db_data}/GNOme.obo.gz
+    curl -L https://glycosmos.org/download/glycosmos_glycans_list.csv \
+        | gzip -c > ${db_data}/glycosmos_glycans_list.csv.gz
+
+
+    echo "Serializing the other databases..."
+    cargo run --bin rustyms-generate-databases
+}
+
+
+function main {
+    while [[ $# -gt 0 ]]; do
+        case "$1" in
+            -h|--help)
+                help
+                ;;
+            *)
+                echo "Unknown argument: $1"
+                help
+                ;;
+        esac
+    done
+
+    touch /tmp/MESSAGES
+
+    make-imgt
+    make-ontologies
+}
+
+
+main "$@"
diff --git a/.gitignore b/.gitignore
index d37079c4..aeaa2116 100644
--- a/.gitignore
+++ b/.gitignore
@@ -1,3 +1,6 @@
+rustyms-generate-databases/data/*
+!rustyms-generate-databases/data/CIAAW*
+!rustyms-generate-databases/data/IUPAC*
 /target
 Cargo.lock
 */target/
@@ -11,4 +14,4 @@ docs/**/_build/
 out
 out_peaks
 out_pro_forma
-out_sloppy_pro_forma
\ No newline at end of file
+out_sloppy_pro_forma
diff --git a/CITATION.cff b/CITATION.cff
new file mode 100644
index 00000000..e65378f0
--- /dev/null
+++ b/CITATION.cff
@@ -0,0 +1,37 @@
+title: rustyms
+version: 0.9.0
+abstract:  A rust library for parsing Pro Forma peptides and matching them against MS spectra .
+authors:
+  - affiliation: Utrecht University
+    family-names: Schulte
+    given-names: Douwe
+    orcid: https://orcid.org/0000-0003-0594-0993
+  - affiliation: VIB-UGent Center for Medical Biotechnology
+    family-names: Gabriels
+    given-names: Ralf
+    orcid: https://orcid.org/0000-0002-1679-1711
+  - affiliation: Utrecht University
+    family-names: Heerdink
+    given-names: Auke
+cff-version: 1.2.0
+identifiers:
+  - description: Main paper (preprint)
+    type: doi
+    value: 10.1101/2025.01.18.633732 
+  - description: Mass alignment algorithm paper
+    type: doi
+    value: 10.1021/acs.jproteome.4c00188
+  - description: Mass alignment algorithm paper (preprint)
+    type: url
+    value: https://www.biorxiv.org/content/10.1101/2024.02.20.581155v1
+  - description: Repository
+    type: url
+    value: https://github.com/snijderlab/rustyms
+keywords:
+  - sequencing
+  - antibody
+  - mass-spectrometry
+  - de novo
+license: MIT OR Apache-2.0
+message: If you use this software, please cite it using these metadata.
+repository-code: https://github.com/snijderlab/rustyms
diff --git a/Cargo.toml b/Cargo.toml
index d761a2d3..2b0e5225 100644
--- a/Cargo.toml
+++ b/Cargo.toml
@@ -15,8 +15,8 @@ package.authors = [
 ]
 package.edition = "2021"
 package.license = "MIT OR Apache-2.0"
-package.rust-version = "1.75.0"
-package.version = "0.9.0-alpha.3"
+package.rust-version = "1.84.0"
+package.version = "0.9.0"
 
 [profile.release]
 debug = true
@@ -29,21 +29,28 @@ codegen-units = 1
 afl = "0.15"
 bincode = "1.3"
 clap = { version = "4.5", features = ["derive", "cargo"] }
-directories = "5.0"
+directories = "6.0"
 flate2 = "1.0"
 iai-callgrind = "0.14"
-itertools = "0.13"
-mzdata = "0.40"
+itertools = "0.14"
+mzdata = "0.44"
 ndarray = "0.16"
-ordered-float = { version = "4.5", features = ["serde"] }
+ordered-float = { version = "4.6", features = ["serde"] }
 probability = "0.20"
 pyo3 = "0.23"
-rand = "0.8"
-rayon = "1.9"
+rand = "0.9"
+rayon = "1.10"
 regex = "1.11"
 roxmltree = "0.20"
 serde = { version = "1.0", features = ["derive", "rc"] }
 serde_json = "1.0"
-similar = "2.6"
+similar = "2.7"
 thin-vec = { version = "0.2", features = ["serde"] }
 uom = { version = "0.36", features = ["use_serde", "usize", "isize"] }
+
+[workspace.lints.rust]
+unexpected_cfgs = { level = "allow", check-cfg = [
+    "cfg(github_action)",
+    "cfg(si)",
+    "cfg(f32)",
+] }
diff --git a/README.md b/README.md
index a97a25b1..75632001 100644
--- a/README.md
+++ b/README.md
@@ -3,22 +3,22 @@
 
 # Match those fragments!
 
-A peptide fragmentation matching library for Rust. Built to handle very complex peptides in a sensible way.
+A peptide fragmentation matching library for Rust. Built to handle very complex peptidoforms in a sensible way.
 
 ## Features
 
- - Read [ProForma](https://github.com/HUPO-PSI/ProForma) sequences (complete specification supported: 'level 2-ProForma + top-down compliant + cross-linking compliant + glycans compliant + mass spectrum compliant')
- - Generate theoretical fragments with control over the fragmentation model from any ProForma peptidoform/proteoform
+ - Read [ProForma](https://github.com/HUPO-PSI/ProForma) sequences (complete 2.0 specification supported: 'level 2-ProForma + top-down compliant + cross-linking compliant + glycans compliant + mass spectrum compliant')
+ - Generate theoretical fragments with control over the fragmentation model from any ProForma peptidoform
    - Generate theoretical fragments for chimeric spectra
    - Generate theoretical fragments for cross-links (also disulfides)
    - Generate theoretical fragments for modifications of unknown position
-   - Generate peptide backbone (a, b, c, x, y, and z) and satellite ion fragments (w, d, and v)
+   - Generate peptide backbone (a, b, c, x, y, and z) and satellite ion fragments (d, v, and w)
    - Generate glycan fragments (B, Y, and internal fragments)
  - Integrated with [mzdata](https://crates.io/crates/mzdata) for reading raw data files
  - Match spectra to the generated fragments
  - [Align peptides based on mass](https://pubs.acs.org/doi/10.1021/acs.jproteome.4c00188)
  - Fast access to the IMGT database of antibody germlines
- - Reading of multiple identified peptide file formats (Fasta, MaxQuant, MSFragger, Novor, OPair, Peaks, and Sage)
+ - Reading of multiple identified peptide file formats (among others: Fasta, MaxQuant, MSFragger, Novor, OPair, Peaks, and Sage)
  - Exhaustively fuzz tested for reliability (using [cargo-afl](https://crates.io/crates/cargo-afl))
  - Extensive use of [uom](https://docs.rs/uom/latest/uom/) for compile time unit checking
  - Python bindings are provided to several core components of the rustyms library. Go to the [Python documentation](https://rustyms.readthedocs.io/) for more information.
diff --git a/docs/python/source/index.md b/docs/python/source/index.md
index 0ef50962..a973fe3f 100644
--- a/docs/python/source/index.md
+++ b/docs/python/source/index.md
@@ -17,7 +17,7 @@ Python bindings are provided to several core components of the rustyms library,
 - {py:class}`~rustyms.Fragment` Theoretical fragment ion
 - {py:class}`~rustyms.SequenceElement` One position in a peptide sequence with amino acid and
   modifications
-- {py:class}`~rustyms.LinearPeptide` Peptide sequence, modifications, and charge, using
+- {py:class}`~rustyms.CompoundPeptidoformIon` Peptide sequence, modifications, and charge, using
   [ProForma 2.0](https://proforma.readthedocs.io) (see {ref}`ProForma support` for more
   information)
 - {py:class}`~rustyms.RawPeak` A single peak in a mass spectrum
@@ -43,7 +43,7 @@ raw_spectrum = rustyms.RawSpectrum(
 )
 
 # Create a new peptide from a ProForma 2.0 string
-peptide = rustyms.LinearPeptide("ACDE/2")
+peptide = rustyms.CompoundPeptidoformIon("ACDE/2")
 
 # Annotate the spectrum with the peptide
 annotated_spectrum = raw_spectrum.annotate(peptide, "cid_hcd")
@@ -68,7 +68,6 @@ rustyms Python bindings.
 :maxdepth: 2
 
 About <self>
-proforma-support
 api
 contributing
 ```
diff --git a/docs/python/source/proforma-support.md b/docs/python/source/proforma-support.md
deleted file mode 100644
index 3d53517e..00000000
--- a/docs/python/source/proforma-support.md
+++ /dev/null
@@ -1,3 +0,0 @@
-```{include} ../../../proforma_grammar.md
-:parser: myst
-```
diff --git a/examples/de-novo-align/Cargo.toml b/examples/de-novo-align/Cargo.toml
index d71764af..5d6392dd 100644
--- a/examples/de-novo-align/Cargo.toml
+++ b/examples/de-novo-align/Cargo.toml
@@ -12,3 +12,6 @@ clap = { workspace = true }
 itertools = { workspace = true }
 rayon = { workspace = true }
 serde_json = { workspace = true }
+
+[lints]
+workspace = true
diff --git a/examples/de-novo-align/src/main.rs b/examples/de-novo-align/src/main.rs
index 198375b8..95800e1b 100644
--- a/examples/de-novo-align/src/main.rs
+++ b/examples/de-novo-align/src/main.rs
@@ -51,7 +51,7 @@ fn main() {
                         peptide,
                         align::<4, SemiAmbiguous, SemiAmbiguous>(
                             db.peptide(),
-                            &linear_peptide,
+                            linear_peptide,
                             AlignScoring::default(),
                             AlignType::EITHER_GLOBAL,
                         ),
diff --git a/examples/multi-annotator/Cargo.toml b/examples/multi-annotator/Cargo.toml
index 59870323..ab3cef9b 100644
--- a/examples/multi-annotator/Cargo.toml
+++ b/examples/multi-annotator/Cargo.toml
@@ -13,3 +13,6 @@ directories = { workspace = true }
 itertools = { workspace = true }
 rayon = { workspace = true }
 serde_json = { workspace = true }
+
+[lints]
+workspace = true
diff --git a/examples/multi-annotator/src/main.rs b/examples/multi-annotator/src/main.rs
index 33499e0d..ae1521c5 100644
--- a/examples/multi-annotator/src/main.rs
+++ b/examples/multi-annotator/src/main.rs
@@ -98,7 +98,7 @@ fn main() {
                     .parse::<usize>()
                     .unwrap();
                 let z = line.index_column("z").unwrap().0.parse::<usize>().unwrap();
-                let peptide = CompoundPeptidoform::pro_forma(
+                let peptide = CompoundPeptidoformIon::pro_forma(
                     line.index_column("sequence").unwrap().0,
                     custom_database.as_ref(),
                 )
diff --git a/fuzz/Cargo.toml b/fuzz/Cargo.toml
index cd432cc7..04bf017a 100644
--- a/fuzz/Cargo.toml
+++ b/fuzz/Cargo.toml
@@ -33,3 +33,6 @@ path = "fuzz_targets/peaks.rs"
 test = false
 doc = false
 bench = false
+
+[lints]
+workspace = true
diff --git a/fuzz/fuzz_targets/peaks.rs b/fuzz/fuzz_targets/peaks.rs
index 028a46bf..78786852 100644
--- a/fuzz/fuzz_targets/peaks.rs
+++ b/fuzz/fuzz_targets/peaks.rs
@@ -21,7 +21,7 @@ impl<'a> StringReader<'a> {
     }
 }
 
-impl<'a> Read for StringReader<'a> {
+impl Read for StringReader<'_> {
     fn read(&mut self, buf: &mut [u8]) -> Result<usize> {
         for (i, item) in buf.iter_mut().enumerate() {
             if let Some(x) = self.iter.next() {
diff --git a/fuzz/fuzz_targets/pro_forma.rs b/fuzz/fuzz_targets/pro_forma.rs
index 7aa41033..c91f0f5b 100644
--- a/fuzz/fuzz_targets/pro_forma.rs
+++ b/fuzz/fuzz_targets/pro_forma.rs
@@ -3,7 +3,7 @@ use afl::*;
 fn main() {
     fuzz!(|data: &[u8]| {
         if let Ok(s) = std::str::from_utf8(data) {
-            let _ = rustyms::CompoundPeptidoform::pro_forma(s, None);
+            let _ = rustyms::CompoundPeptidoformIon::pro_forma(s, None);
         }
     });
 }
diff --git a/fuzz/fuzz_targets/sloppy_pro_forma.rs b/fuzz/fuzz_targets/sloppy_pro_forma.rs
index 31f86f9c..d7d0cc4d 100644
--- a/fuzz/fuzz_targets/sloppy_pro_forma.rs
+++ b/fuzz/fuzz_targets/sloppy_pro_forma.rs
@@ -3,7 +3,7 @@ use afl::*;
 fn main() {
     fuzz!(|data: &[u8]| {
         if let Ok(s) = std::str::from_utf8(data) {
-            let _ = rustyms::LinearPeptide::sloppy_pro_forma(
+            let _ = rustyms::Peptidoform::sloppy_pro_forma(
                 s,
                 0..s.len(),
                 None,
diff --git a/rustyms-generate-databases/Cargo.toml b/rustyms-generate-databases/Cargo.toml
index ab1b2429..339297f2 100644
--- a/rustyms-generate-databases/Cargo.toml
+++ b/rustyms-generate-databases/Cargo.toml
@@ -20,3 +20,6 @@ uom = { workspace = true }
 
 [features]
 rayon = []
+
+[lints]
+workspace = true
diff --git a/rustyms-generate-databases/data/GNOme.obo.gz b/rustyms-generate-databases/data/GNOme.obo.gz
deleted file mode 100644
index d0e1f3e2..00000000
Binary files a/rustyms-generate-databases/data/GNOme.obo.gz and /dev/null differ
diff --git a/rustyms-generate-databases/data/PSI-MOD-newstyle.obo b/rustyms-generate-databases/data/PSI-MOD-newstyle.obo
deleted file mode 100644
index a05e132d..00000000
--- a/rustyms-generate-databases/data/PSI-MOD-newstyle.obo
+++ /dev/null
@@ -1,37537 +0,0 @@
-format-version: 1.2
-ontology: mod
-date: 13:06:2021 12:12
-saved-by: Charles Tapley Hoyt
-subsetdef: PSI-MOD-slim "subset of protein modifications"
-synonymtypedef: DeltaMass-label "Label from MS DeltaMass" EXACT
-synonymtypedef: OMSSA-label "Short label from OMSSA" EXACT
-synonymtypedef: PSI-MOD-alternate "Alternate name curated by PSI-MOD" EXACT
-synonymtypedef: PSI-MOD-label "Short label curated by PSI-MOD" EXACT
-synonymtypedef: PSI-MS-label "Agreed label from MS community" RELATED
-synonymtypedef: RESID-alternate "Alternate name from RESID" EXACT
-synonymtypedef: RESID-misnomer "Misnomer tagged alternate name from RESID" RELATED
-synonymtypedef: RESID-name "Name from RESID" EXACT
-synonymtypedef: RESID-systematic "Systematic name from RESID" EXACT
-synonymtypedef: Unimod-alternate "Alternate name from Unimod" RELATED
-synonymtypedef: Unimod-description "Description (full_name) from Unimod" RELATED
-synonymtypedef: Unimod-interim "Interim label from Unimod" RELATED
-synonymtypedef: UniProt-feature "Protein feature description from UniProtKB" EXACT
-default-namespace: PSI-MOD
-data-version: 1.031.5
-remark: PSI-MOD version: 1.031.5
-remark: RESID release: 75.00
-remark: ISO-8601 date: 2022-06-13 12:12Z
-remark: Annotation note 01 - \"[PSI-MOD:ref]\" has been replaced by PubMed:18688235.
-remark: Annotation note 02 - When an entry in the RESID Database is annotated with different sources because the same modification can arise from different encoded amino acids, then the PSI-MOD definition for each different source instance carries the RESID cross-reference followed by a hash symbol \"#\" and a 3 or 4 character label. When an entry in the RESID Database is annotated as a general modification with the same enzymatic activity producing different chemical structures depending on natural variation in the nonproteinaceous substrate, on secondary modifications that do not change the nature of the primary modification, or on a combination of a primary and one or more secondary modifications on the same residue, then the PSI-MOD definition for each different instance carries the RESID cross-reference followed by the special tag \"#var\".
-remark: Annotation note 03 - When an entry in the Unimod database is annotated as a general modification, and one or more instance sites are listed, then the PSI-MOD definition for each different site instance carries the Unimod cross-reference followed by a hash symbol and an amino acid code, \"N-term\" or \"C-term\".
-remark: Annotation note 04 - The elemental formulas are in strict alphabetical order, not in CAS (\"C\" and \"H\" first) order. Isotope numbers are in parentheses before the element symbol, and an element should not occur in a formula both with and without an isotope number. In difference formulas, counts can be zero or negative.
-remark: Annotation note 05 - In entries with an isotope indicator in the formula, average masses are meaningless and are assigned the value equal to the monoisotopic mass, but rounded to a lower precision; monoisotopic masses are calculated by using the masses for the indicated isotopes and the most common isotopes for other elements without isotope indicators in the formulas.
-remark: Annotation note 06 - For cross-link modifications, the number following \"Cross-link\" in the comment record indicates the number of amino acid residues that appear in the origin record, used to check the difference formula and masses. This usage differs from RESID, where the cross-link number indicates the maximum number of peptide chains that can be cross-linked.
-remark: Annotation note 07 - The synonym cross-reference \"MOD:old name\" has been replaced by \"MOD:alternate name\".
-remark: Annotation note 08 - The DeltaMass listings for free amino acids have been removed. Most Unimod entries that have not been \"approved\" have by general agreement not been incorporated unless there has been a request for a specific term by a PRIDE submitter.
-remark: Annotation note 09 - The Open Mass Spectrometry Search Algorithm, OMSSA, enumerated list of modifications are being incorporated. The string values are synonyms with the synonymtypedef \"OMSSA-label\", and their integer values (which are supposed to be stable) are definition cross-references.
-remark: Annotation note 10 - GNOme is the Glycan Naming and Subsumption Ontology (https://gnome.glyomics.org/), an ontology for the support of glycomics.  PSI-MOD does not have all possible glycans in its entries, just the ones that are noted to be on proteins and have been requested for addition.  GNOme uses GlyTouCan (http://glytoucan.org/) to provide stable accessions for glycans described at varyious degrees of characterization, including compositions (no linkage) and topologies (no carbon bond positions or anomeric configurations).
-idspace: uniprot.ptm https://bioregistry.io/uniprot.ptm: "UniProt Post-Translational Modification"
-
-[Term]
-id: MOD:00000
-name: protein modification
-def: "Covalent modification of, or a change resulting in an alteration of the measured molecular mass of, a peptide or protein amino acid residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "ModRes" EXACT PSI-MOD-label []
-
-[Term]
-id: MOD:00001
-name: alkylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with an alkyl group." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "AlkylRes" EXACT PSI-MOD-label []
-is_a: MOD:01156
-
-[Term]
-id: MOD:00002
-name: O-glycosyl-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O3-glycosylserine." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "OGlycoSer" EXACT PSI-MOD-label []
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00396
-is_a: MOD:00916
-
-[Term]
-id: MOD:00003
-name: Unimod
-def: "Entry from Unimod." [PubMed:18688235]
-comment: This term is for organizational use only and should not be assigned. [JSG]
-is_a: MOD:00032
-
-[Term]
-id: MOD:00004
-name: artifact
-def: "Artifact entry from Unimod - OBSOLETE because organizational use is no longer required." [PubMed:18688235]
-is_obsolete: true
-
-[Term]
-id: MOD:00005
-name: O-glycosyl-L-threonine
-def: "A protein modification that effectively converts an L-threonine residue to O3-glycosylthreonine." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "OGlycoThr" EXACT PSI-MOD-label []
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00396
-is_a: MOD:00917
-
-[Term]
-id: MOD:00006
-name: N-glycosylated residue
-def: "A protein modification that effectively replaces a residue hydrogen atom on a nitrogen with a carbohydrate-like group through a glycosidic bond." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "NGlycoRes" EXACT PSI-MOD-label []
-is_a: MOD:00693
-
-[Term]
-id: MOD:00007
-name: selenium substitution for sulfur
-def: "A protein modification that effectively substitutes a selenium atom for a sulfur atom." [PubMed:12148805, Unimod:162]
-synonym: "Delta:S(-1)Se(1)" RELATED PSI-MS-label []
-synonym: "Se(S)Res" EXACT PSI-MOD-label []
-synonym: "Selenium replaces sulphur" RELATED Unimod-description []
-property_value: DiffAvg "46.91" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0 S -1 Se 1" xsd:string
-property_value: DiffMono "47.944450" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:162
-is_a: MOD:00745
-
-[Term]
-id: MOD:00008
-name: common
-def: "Entry from Unimod representing one or more entries in RESID. OBSOLETE because organizational use is no longer required." [PubMed:18688235]
-is_obsolete: true
-
-[Term]
-id: MOD:00009
-name: natural residue
-def: "A protein modification that removes a residue, or inserts or replaces a residue with a natural, standard or nonstandard, encoded residue." [PubMed:6692818, RESID:AA0000]
-subset: PSI-MOD-slim
-synonym: "alpha-amino acid" EXACT RESID-name []
-synonym: "Res" EXACT PSI-MOD-label []
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:01157
-
-[Term]
-id: MOD:00010
-name: L-alanine residue
-def: "A protein modification that effectively converts a source amino acid residue to an L-alanine." [ChEBI:29948, DeltaMass:0, PubMed:6692818, RESID:AA0001]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-aminopropanoic acid" EXACT RESID-systematic []
-synonym: "2-aminopropionic acid" EXACT RESID-alternate []
-synonym: "2-azanylpropanoic acid" EXACT RESID-alternate []
-synonym: "Ala" EXACT PSI-MOD-label []
-synonym: "alpha-alanine" EXACT RESID-alternate []
-synonym: "alpha-aminopropionic acid" EXACT RESID-alternate []
-synonym: "L-alanine" EXACT RESID-name []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 3 H 5 N 1 O 1" xsd:string
-property_value: MassAvg "71.08" xsd:float
-property_value: MassMono "71.037114" xsd:float
-property_value: Origin "A" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00570
-is_a: MOD:00859
-is_a: MOD:01441
-
-[Term]
-id: MOD:00011
-name: L-arginine residue
-def: "A protein modification that effectively converts a source amino acid residue to an L-arginine." [ChEBI:29952, DeltaMass:0, PubMed:518876, PubMed:6692818, RESID:AA0002]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-5-[(diaminomethylidene)amino]pentanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-5-(carbamimidamido)pentanoic acid [tautomer]" EXACT RESID-alternate []
-synonym: "2-amino-5-[(aminoiminomethyl)amino]pentanoic acid [tautomer]" EXACT RESID-alternate []
-synonym: "2-amino-5-guanidinopentanoic acid" EXACT RESID-alternate []
-synonym: "2-amino-5-guanidinovaleric acid" EXACT RESID-alternate []
-synonym: "2-azanyl-5-[bis(azanyl)methylideneazanyl]pentanoic acid" EXACT RESID-alternate []
-synonym: "alpha-amino-delta-guanidinovaleric acid" EXACT RESID-alternate []
-synonym: "Arg" EXACT PSI-MOD-label []
-synonym: "L-arginine" EXACT RESID-name []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 6 H 12 N 4 O 1" xsd:string
-property_value: MassAvg "156.19" xsd:float
-property_value: MassMono "156.101111" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:01441
-
-[Term]
-id: MOD:00012
-name: L-asparagine residue
-def: "A protein modification that effectively converts a source amino acid residue to an L-asparagine." [ChEBI:29956, DeltaMass:0, PubMed:15736973, PubMed:5681232, PubMed:6692818, PubMed:9789001, RESID:AA0003]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-4-butanediamic acid" EXACT RESID-systematic []
-synonym: "2,4-bis(azanyl)-4-oxobutanoic acid" EXACT RESID-alternate []
-synonym: "2,4-diamino-4-oxobutanoic acid" EXACT RESID-alternate []
-synonym: "2-amino-3-carbamoylpropanoic acid" EXACT RESID-alternate []
-synonym: "2-amino-4-butanediamic acid" EXACT RESID-alternate []
-synonym: "2-aminosuccinamic acid" EXACT RESID-alternate []
-synonym: "2-aminosuccinic acid 4-amide" EXACT RESID-alternate []
-synonym: "alpha-amino-beta-carbamylpropionic acid" EXACT RESID-alternate []
-synonym: "alpha-aminosuccinamic acid" EXACT RESID-alternate []
-synonym: "Asn" EXACT PSI-MOD-label []
-synonym: "aspartic acid 4-amide" EXACT RESID-alternate []
-synonym: "aspartic acid beta-amide" EXACT RESID-alternate []
-synonym: "beta-asparagine" EXACT RESID-alternate []
-synonym: "L-asparagine" EXACT RESID-name []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 4 H 6 N 2 O 2" xsd:string
-property_value: MassAvg "114.10" xsd:float
-property_value: MassMono "114.042927" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00859
-is_a: MOD:01441
-
-[Term]
-id: MOD:00013
-name: L-aspartic acid residue
-def: "A protein modification that effectively converts a source amino acid residue to an L-aspartic acid." [ChEBI:29958, DeltaMass:0, PubMed:1097438, PubMed:339692, PubMed:4399050, PubMed:5764436, PubMed:6692818, PubMed:8089117, PubMed:9521123, PubMed:9582379, RESID:AA0004]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-aminobutanedioic acid" EXACT RESID-systematic []
-synonym: "2-azanylbutanedioic acid" EXACT RESID-alternate []
-synonym: "aminosuccinic acid" EXACT RESID-alternate []
-synonym: "Asp" EXACT PSI-MOD-label []
-synonym: "L-aspartic acid" EXACT RESID-name []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 4 H 5 N 1 O 3" xsd:string
-property_value: MassAvg "115.09" xsd:float
-property_value: MassMono "115.026943" xsd:float
-property_value: Origin "D" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00859
-is_a: MOD:01441
-
-[Term]
-id: MOD:00014
-name: L-cysteine residue
-def: "A protein modification that effectively converts a source amino acid residue to an L-cysteine." [ChEBI:29950, DeltaMass:0, PubMed:1310545, PubMed:15790858, PubMed:3447159, PubMed:6692818, PubMed:7338899, RESID:AA0005]
-comment: From DeltaMass: Average Mass: 121.
-subset: PSI-MOD-slim
-synonym: "(2R)-2-amino-3-sulfanylpropanoic acid" EXACT RESID-systematic []
-synonym: "(R)-cysteine" EXACT RESID-alternate []
-synonym: "2-amino-3-mercaptopropanoic acid" EXACT RESID-alternate []
-synonym: "2-amino-3-mercaptopropionic acid" EXACT RESID-alternate []
-synonym: "2-azanyl-3-sulfanylpropanoic acid" EXACT RESID-alternate []
-synonym: "3-mercapto-L-alanine" EXACT RESID-alternate []
-synonym: "alpha-amino-beta-mercaptopropanoic acid" EXACT RESID-alternate []
-synonym: "alpha-amino-beta-mercaptopropionic acid" EXACT RESID-alternate []
-synonym: "alpha-amino-beta-thiolpropionic acid" EXACT RESID-alternate []
-synonym: "beta-mercaptoalanine" EXACT RESID-alternate []
-synonym: "Cys" EXACT PSI-MOD-label []
-synonym: "Cysteine (C, Cys)" EXACT DeltaMass-label []
-synonym: "half-cystine" EXACT RESID-alternate []
-synonym: "L-(+)-cysteine" EXACT RESID-alternate []
-synonym: "L-cysteine" EXACT RESID-name []
-synonym: "thioserine" EXACT RESID-alternate []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 3 H 5 N 1 O 1 S 1" xsd:string
-property_value: MassAvg "103.14" xsd:float
-property_value: MassMono "103.009185" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00859
-is_a: MOD:01441
-
-[Term]
-id: MOD:00015
-name: L-glutamic acid residue
-def: "A protein modification that effectively converts a source amino acid residue to an L-glutamic acid." [ChEBI:29972, DeltaMass:0, PubMed:1881881, PubMed:4565668, PubMed:4922541, PubMed:6692818, PubMed:9326660, PubMed:957425, RESID:AA0006]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-aminopentanedioic acid" EXACT RESID-systematic []
-synonym: "1-aminopropane-1,3-dicarboxylic acid" EXACT RESID-alternate []
-synonym: "2-aminoglutaric acid" EXACT RESID-alternate []
-synonym: "2-azanylpentanedioic acid" EXACT RESID-alternate []
-synonym: "alpha-aminoglutaric acid" EXACT RESID-alternate []
-synonym: "Glu" EXACT PSI-MOD-label []
-synonym: "glutaminic acid" EXACT RESID-alternate []
-synonym: "L-glutamic acid" EXACT RESID-name []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 5 H 7 N 1 O 3" xsd:string
-property_value: MassAvg "129.12" xsd:float
-property_value: MassMono "129.042593" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00859
-is_a: MOD:01441
-
-[Term]
-id: MOD:00016
-name: L-glutamine residue
-def: "A protein modification that effectively converts a source amino acid residue to an L-glutamine." [ChEBI:30011, DeltaMass:0, PubMed:3340166, PubMed:6692818, PubMed:9342308, RESID:AA0007]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-5-pentanediamic acid" EXACT RESID-systematic []
-synonym: "2,5-bis(azanyl)-5-oxopentanoic acid" EXACT RESID-alternate []
-synonym: "2,5-diamino-5-oxopentanoic acid" EXACT RESID-alternate []
-synonym: "2-amino-4-carbamoylbutanoic acid" EXACT RESID-alternate []
-synonym: "2-aminoglutaramic acid" EXACT RESID-alternate []
-synonym: "alpha-amino-gamma-carbamylbutyric acid" EXACT RESID-alternate []
-synonym: "Gln" EXACT PSI-MOD-label []
-synonym: "glutamic acid 5-amide" EXACT RESID-alternate []
-synonym: "glutamic acid gamma-amide" EXACT RESID-alternate []
-synonym: "glutamide" EXACT RESID-alternate []
-synonym: "L-glutamine" EXACT RESID-name []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 5 H 8 N 2 O 2" xsd:string
-property_value: MassAvg "128.13" xsd:float
-property_value: MassMono "128.058578" xsd:float
-property_value: Origin "Q" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00894
-is_a: MOD:01441
-
-[Term]
-id: MOD:00017
-name: glycine residue
-def: "A protein modification that effectively converts a source amino acid residue to a glycine." [ChEBI:29947, DeltaMass:0, PubMed:1310545, PubMed:6692818, RESID:AA0008]
-subset: PSI-MOD-slim
-synonym: "aminoacetic acid" EXACT RESID-alternate []
-synonym: "aminoethanoic acid" EXACT RESID-systematic []
-synonym: "azanylethanoic acid" EXACT RESID-alternate []
-synonym: "Gly" EXACT PSI-MOD-label []
-synonym: "glycine" EXACT RESID-name []
-synonym: "glycocoll" EXACT RESID-alternate []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 2 H 3 N 1 O 1" xsd:string
-property_value: MassAvg "57.05" xsd:float
-property_value: MassMono "57.021464" xsd:float
-property_value: Origin "G" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:01441
-
-[Term]
-id: MOD:00018
-name: L-histidine residue
-def: "A protein modification that effectively converts a source amino acid residue to an L-histidine." [ChEBI:29979, DeltaMass:0, PubMed:14342316, PubMed:2722967, PubMed:512, PubMed:5460889, PubMed:6129252, PubMed:6692818, PubMed:6876174, RESID:AA0009]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-(1H-imidazol-4-yl)propanoic acid" EXACT RESID-systematic []
-synonym: "(2S)-2-amino-3-(1H-imidazol-5-yl)propanoic acid [tautomer]" EXACT RESID-alternate []
-synonym: "2-azanyl-3-(1H-imidazol-4-yl)propanoic acid" EXACT RESID-alternate []
-synonym: "2-azanyl-3-(1H-imidazol-5-yl)propanoic acid [tautomer]" EXACT RESID-alternate []
-synonym: "4-(2-amino-2-carboxyethyl)imidazole" EXACT RESID-alternate []
-synonym: "alpha-amino-beta-(4-imidazole)propionic acid" EXACT RESID-alternate []
-synonym: "glyoxaline-5-alanine" EXACT RESID-alternate []
-synonym: "His" EXACT PSI-MOD-label []
-synonym: "L-histidine" EXACT RESID-name []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 6 H 7 N 3 O 1" xsd:string
-property_value: MassAvg "137.14" xsd:float
-property_value: MassMono "137.058912" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:01441
-
-[Term]
-id: MOD:00019
-name: L-isoleucine residue
-def: "A protein modification that effectively converts a source amino acid residue to an L-isoleucine." [ChEBI:30009, DeltaMass:0, PubMed:6692818, RESID:AA0010]
-subset: PSI-MOD-slim
-synonym: "(2S,3S)-2-amino-3-methylpentanoic acid" EXACT RESID-systematic []
-synonym: "2-azanyl-3-methylpentanoic acid" EXACT RESID-alternate []
-synonym: "3-methyl-norvaline" EXACT RESID-alternate []
-synonym: "alpha-amino-beta-methylvaleric acid" EXACT RESID-alternate []
-synonym: "Ile" EXACT PSI-MOD-label []
-synonym: "Isoleucyl" EXACT DeltaMass-label []
-synonym: "L-erythro-isoleucine" EXACT RESID-alternate []
-synonym: "L-isoleucine" EXACT RESID-name []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 6 H 11 N 1 O 1" xsd:string
-property_value: MassAvg "113.16" xsd:float
-property_value: MassMono "113.084064" xsd:float
-property_value: Origin "I" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00306
-is_a: MOD:01441
-
-[Term]
-id: MOD:00020
-name: L-leucine residue
-def: "A protein modification that effectively converts a source amino acid residue to an L-leucine." [ChEBI:30006, DeltaMass:0, PubMed:11478885, PubMed:6692818, RESID:AA0011]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-4-methylpentanoic acid" EXACT RESID-systematic []
-synonym: "2-azanyl-4-methylpentanoic acid" EXACT RESID-alternate []
-synonym: "4-methyl-norvaline" EXACT RESID-alternate []
-synonym: "alpha-amino-gamma-methylvaleric acid" EXACT RESID-alternate []
-synonym: "alpha-aminoisocaproic acid" EXACT RESID-alternate []
-synonym: "L-leucine" EXACT RESID-name []
-synonym: "Leu" EXACT PSI-MOD-label []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 6 H 11 N 1 O 1" xsd:string
-property_value: MassAvg "113.16" xsd:float
-property_value: MassMono "113.084064" xsd:float
-property_value: Origin "L" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00306
-is_a: MOD:01441
-
-[Term]
-id: MOD:00021
-name: L-lysine residue
-def: "A protein modification that effectively converts a source amino acid residue to L-lysine." [ChEBI:29967, DeltaMass:0, PubMed:3106962, PubMed:6120171, PubMed:6692818, RESID:AA0012]
-subset: PSI-MOD-slim
-synonym: "(2S)-2,6-diaminohexanoic acid" EXACT RESID-systematic []
-synonym: "2,6-bis(azanyl)hexanoic acid" EXACT RESID-alternate []
-synonym: "6-amino-L-norleucine" EXACT RESID-alternate []
-synonym: "ACT_SITE Schiff-base intermediate with substrate" EXACT UniProt-feature []
-synonym: "alpha,epsilon-diaminocaproic acid" EXACT RESID-alternate []
-synonym: "L-lysine" EXACT RESID-name []
-synonym: "Lys" EXACT PSI-MOD-label []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 6 H 12 N 2 O 1" xsd:string
-property_value: MassAvg "128.18" xsd:float
-property_value: MassMono "128.094963" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00893
-is_a: MOD:01441
-
-[Term]
-id: MOD:00022
-name: L-methionine residue
-def: "A protein modification that effectively converts a source amino acid residue to L-methionine." [ChEBI:29983, DeltaMass:0, PubMed:6411710, PubMed:6692818, RESID:AA0013]
-comment: From DeltaMass: Average Mass: 149
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-4-(methylsulfanyl)butanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-4-(methylthio)butanoic acid" EXACT RESID-alternate []
-synonym: "2-amino-4-(methylthio)butyric acid" EXACT RESID-alternate []
-synonym: "2-azanyl-4-(methylsulfanyl)butanoic acid" EXACT RESID-alternate []
-synonym: "alpha-amino-gamma-methylmercaptobutyric acid" EXACT RESID-alternate []
-synonym: "alpha-amino-gamma-methylthiobutyric acid" EXACT RESID-alternate []
-synonym: "gamma-methylthio-alpha-aminobutyric acid" EXACT RESID-alternate []
-synonym: "L-(-)-methionine" EXACT RESID-alternate []
-synonym: "L-methionine" EXACT RESID-name []
-synonym: "Met" EXACT PSI-MOD-label []
-synonym: "S-methyl-L-homocysteine" EXACT RESID-alternate []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 5 H 9 N 1 O 1 S 1" xsd:string
-property_value: MassAvg "131.19" xsd:float
-property_value: MassMono "131.040485" xsd:float
-property_value: Origin "M" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:01441
-
-[Term]
-id: MOD:00023
-name: L-phenylalanine residue
-def: "A protein modification that effectively converts a source amino acid residue to L-phenylalanine." [ChEBI:29997, DeltaMass:0, PubMed:6692818, RESID:AA0014]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-phenylpropanoic acid" EXACT RESID-systematic []
-synonym: "2-azanyl-3-phenylpropanoic acid" EXACT RESID-alternate []
-synonym: "alpha-amino-beta-phenylpropionic acid" EXACT RESID-alternate []
-synonym: "L-phenylalanine" EXACT RESID-name []
-synonym: "Phe" EXACT PSI-MOD-label []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 9 H 9 N 1 O 1" xsd:string
-property_value: MassAvg "147.18" xsd:float
-property_value: MassMono "147.068414" xsd:float
-property_value: Origin "F" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:01441
-
-[Term]
-id: MOD:00024
-name: L-proline residue
-def: "A protein modification that effectively converts a source amino acid residue to L-proline." [ChEBI:30017, DeltaMass:0, PubMed:6692818, PubMed:8547259, RESID:AA0015]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-pyrrolidinecarboxylic acid" EXACT RESID-systematic []
-synonym: "L-proline" EXACT RESID-name []
-synonym: "Pro" EXACT PSI-MOD-label []
-synonym: "pyrrolidine-2-carboxylic acid" EXACT RESID-alternate []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 5 H 7 N 1 O 1" xsd:string
-property_value: MassAvg "97.12" xsd:float
-property_value: MassMono "97.052764" xsd:float
-property_value: Origin "P" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:01441
-
-[Term]
-id: MOD:00025
-name: L-serine residue
-def: "A protein modification that effectively converts a source amino acid residue to L-serine." [ChEBI:29999, DeltaMass:0, PubMed:4399050, PubMed:6692818, RESID:AA0016]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-hydroxypropanoic acid" EXACT RESID-systematic []
-synonym: "2-azanyl-3-hydroxypropanoic acid" EXACT RESID-alternate []
-synonym: "3-hydroxy-L-alanine" EXACT RESID-alternate []
-synonym: "alpha-amino-beta-hydroxypropionic acid" EXACT RESID-alternate []
-synonym: "beta-hydroxyalanine" EXACT RESID-alternate []
-synonym: "L-serine" EXACT RESID-name []
-synonym: "Ser" EXACT PSI-MOD-label []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 3 H 5 N 1 O 2" xsd:string
-property_value: MassAvg "87.08" xsd:float
-property_value: MassMono "87.032028" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:01441
-
-[Term]
-id: MOD:00026
-name: L-threonine residue
-def: "A protein modification that effectively converts a source amino acid residue to L-threonine." [ChEBI:30013, DeltaMass:0, PubMed:2989287, PubMed:6692818, RESID:AA0017]
-subset: PSI-MOD-slim
-synonym: "(2S,3R)-2-amino-3-hydroxybutanoic acid" EXACT RESID-systematic []
-synonym: "2-azanyl-3-hydroxybutanoic acid" EXACT RESID-alternate []
-synonym: "alpha-amino-beta-hydroxybutyric acid" EXACT RESID-alternate []
-synonym: "beta-methylserine" EXACT RESID-alternate []
-synonym: "L-threo-threonine" EXACT RESID-alternate []
-synonym: "L-threonine" EXACT RESID-name []
-synonym: "Thr" EXACT PSI-MOD-label []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 4 H 7 N 1 O 2" xsd:string
-property_value: MassAvg "101.10" xsd:float
-property_value: MassMono "101.047678" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:01441
-
-[Term]
-id: MOD:00027
-name: L-tryptophan residue
-def: "A protein modification that effectively converts a source amino acid residue to L-tryptophan." [ChEBI:29954, DeltaMass:0, PubMed:2059637, PubMed:6692818, PubMed:9324768, RESID:AA0018]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-(1H-indol-3-yl)propanoic acid" EXACT RESID-systematic []
-synonym: "2-azanyl-3-(1H-indol-3-yl)propanoic acid" EXACT RESID-alternate []
-synonym: "alpha-amino-beta-(3-indolyl)propionoic acid" EXACT RESID-alternate []
-synonym: "beta(3-indolyl)alanine" EXACT RESID-alternate []
-synonym: "L-tryptophan" EXACT RESID-name []
-synonym: "Trp" EXACT PSI-MOD-label []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 11 H 10 N 2 O 1" xsd:string
-property_value: MassAvg "186.21" xsd:float
-property_value: MassMono "186.079313" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:01441
-
-[Term]
-id: MOD:00028
-name: L-tyrosine residue
-def: "A protein modification that effectively converts a source amino acid residue to L-tyrosine." [ChEBI:29975, DeltaMass:0, PubMed:2190093, PubMed:2542938, PubMed:5550972, PubMed:6061414, PubMed:6120171, PubMed:6692818, RESID:AA0019]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-(4-hydoxyphenyl)propanoic acid" EXACT RESID-systematic []
-synonym: "2-azanyl-3-(4-hydoxyphenyl)propanoic acid" EXACT RESID-alternate []
-synonym: "alpha-amino-beta-(para-hydroxyphenyl)propionic acid" EXACT RESID-alternate []
-synonym: "L-tyrosine" EXACT RESID-name []
-synonym: "p-tyrosine" EXACT RESID-alternate []
-synonym: "para-hydroxyphenylalanine" EXACT RESID-alternate []
-synonym: "Tyr" EXACT PSI-MOD-label []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 9 H 9 N 1 O 2" xsd:string
-property_value: MassAvg "163.18" xsd:float
-property_value: MassMono "163.063329" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:01441
-
-[Term]
-id: MOD:00029
-name: L-valine residue
-def: "A protein modification that effectively converts a source amino acid residue to an L-valine." [ChEBI:30015, DeltaMass:0, PubMed:6692818, RESID:AA0020]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-methylbutanoic acid" EXACT RESID-systematic []
-synonym: "2-azanyl-3-methylbutanoic acid" EXACT RESID-alternate []
-synonym: "alpha-amino-beta-methylbutyric acid" EXACT RESID-alternate []
-synonym: "alpha-aminoisovaleric acid" EXACT RESID-alternate []
-synonym: "L-valine" EXACT RESID-name []
-synonym: "Val" EXACT PSI-MOD-label []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 5 H 9 N 1 O 1" xsd:string
-property_value: MassAvg "99.13" xsd:float
-property_value: MassMono "99.068414" xsd:float
-property_value: Origin "V" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:01441
-
-[Term]
-id: MOD:00030
-name: N-formyl-L-methionine residue
-def: "A protein modification that effectively converts a source amino acid residue to an N-formyl-L-methionine, a natural pretranslational modification." [ChEBI:33718, OMSSA:22, PubMed:10825024, PubMed:11152118, PubMed:2165784, PubMed:3042771, PubMed:8758896, RESID:AA0021#FMET]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-formylamino-4-(methylsulfanyl)butanoic acid" EXACT RESID-systematic []
-synonym: "2-formamido-4-(methylsulfanyl)butanoic acid" EXACT RESID-alternate []
-synonym: "2-formylamino-4-(methylthio)butanoic acid" EXACT RESID-alternate []
-synonym: "2-formylazanyl-4-(methylsulfanyl)butanoic acid" EXACT RESID-alternate []
-synonym: "fMet" EXACT PSI-MOD-label []
-synonym: "FormylMet" RELATED PSI-MS-label []
-synonym: "MOD_RES N-formylmethionine" EXACT UniProt-feature []
-synonym: "N-formyl-L-methionine" EXACT RESID-name []
-synonym: "N-formylated L-methionine" EXACT PSI-MOD-alternate []
-synonym: "nformylmet" EXACT OMSSA-label []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 6 H 10 N 1 O 2 S 1" xsd:string
-property_value: MassAvg "160.21" xsd:float
-property_value: MassMono "160.043225" xsd:float
-property_value: Origin "M" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00868
-
-[Term]
-id: MOD:00031
-name: L-selenocysteine residue
-def: "A protein modification that effectively converts a source amino acid residue to an L-selenocysteine, a natural pretranslational modification." [ChEBI:30000, PubMed:10523135, PubMed:1066676, PubMed:2037562, PubMed:2963330, PubMed:4734725, PubMed:6076213, PubMed:6217842, PubMed:6714945, RESID:AA0022]
-subset: PSI-MOD-slim
-synonym: "(2R)-2-amino-3-selanylpropanoic acid" EXACT RESID-systematic []
-synonym: "2-azanyl-3-selanylpropanoic acid" EXACT RESID-alternate []
-synonym: "3-selenylalanine" EXACT RESID-alternate []
-synonym: "L-selenocysteine" EXACT RESID-name []
-synonym: "NON_STD Selenocysteine" EXACT UniProt-feature []
-synonym: "Sec" EXACT PSI-MOD-label []
-synonym: "SeCys" EXACT RESID-alternate []
-synonym: "selenium cysteine" EXACT RESID-alternate []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0 Se 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 3 H 5 N 1 O 1 Se 1" xsd:string
-property_value: MassAvg "150.05" xsd:float
-property_value: MassMono "150.953635" xsd:float
-property_value: Origin "U" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00745
-is_a: MOD:00859
-is_a: MOD:00868
-
-[Term]
-id: MOD:00032
-name: uncategorized protein modification
-def: "A protein modification that is not chemically categorized." [PubMed:18688235]
-comment: This term is for organizational use only and should not be assigned. [JSG]
-is_a: MOD:00000
-
-[Term]
-id: MOD:00033
-name: crosslinked residues
-def: "A protein modification that crosslinks two or more amino acid residues with covalent bonds." [PubMed:18688235]
-comment: The covalent bond is formed directly between sidechain atoms. If non-aminoacid atoms are involved in connecting two or more peptide chain residues peptide chain, the connection is classified as a multivalent binding site.
-subset: PSI-MOD-slim
-synonym: "XLNK-Res-Res" EXACT PSI-MOD-label []
-is_a: MOD:01156
-
-[Term]
-id: MOD:00034
-name: L-cystine (cross-link)
-def: "A protein modification that effectively cross-links two L-cysteine residues to form L-cystine." [ChEBI:16283, DeltaMass:0, PubMed:1988019, PubMed:2001356, PubMed:2076469, PubMed:3083866, PubMed:366603, PubMed:7918467, PubMed:8344916, RESID:AA0025#CYS2]
-comment: Cross-link 2; for formation of a disulfide bond between a peptide cysteine and a free cysteine, see MOD:00765.
-subset: PSI-MOD-slim
-synonym: "(2R,2'R)-3,3'-disulfane-1,2-diylbis(2-aminopropanoic acid)" EXACT RESID-systematic []
-synonym: "2-amino-3-(2-amino-2-carboxy-ethyl)disulfanyl-propanoic acid" RELATED RESID-misnomer []
-synonym: "3,3'-disulfane-1,2-diylbis(2-azanylpropanoic acid)" EXACT RESID-alternate []
-synonym: "3,3'-dithiobis(2-aminopropanoic acid)" EXACT RESID-alternate []
-synonym: "3,3'-dithiobisalanine" EXACT RESID-alternate []
-synonym: "3,3'-dithiodialanine" EXACT RESID-alternate []
-synonym: "beta,beta'-diamino-beta,beta'-dicarboxydiethyldisulfide" EXACT RESID-alternate []
-synonym: "beta,beta'-dithiodialanine" EXACT RESID-alternate []
-synonym: "bis(alpha-aminopropionic acid)-beta-disulfide" EXACT RESID-alternate []
-synonym: "bis(beta-amino-beta-carboxyethyl)disulfide" EXACT RESID-alternate []
-synonym: "Cys2" EXACT PSI-MOD-label []
-synonym: "Cystine ((Cys)2)" EXACT DeltaMass-label []
-synonym: "dicysteine" EXACT RESID-alternate []
-synonym: "DISULFID" EXACT UniProt-feature []
-synonym: "DISULFID Interchain" EXACT UniProt-feature []
-synonym: "L-cystine" EXACT RESID-name []
-synonym: "XLNK-SCys-SCys" EXACT PSI-MOD-label []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 6 H 8 N 2 O 2 S 2" xsd:string
-property_value: MassAvg "204.26" xsd:float
-property_value: MassMono "204.002720" xsd:float
-property_value: Origin "C, C" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00689
-
-[Term]
-id: MOD:00035
-name: (2S,3R)-3-hydroxyasparagine
-def: "A protein modification that effectively converts an L-asparagine residue to (2S,3R)-3-hydroxyasparagine." [PubMed:11823643, PubMed:2820791, RESID:AA0026, ChEBI:141853]
-subset: PSI-MOD-slim
-synonym: "(2S,3R)-2,4-diamino-3-hydroxy-4-oxobutanoic acid" EXACT RESID-alternate []
-synonym: "(2S,3R)-2-amino-3-hydroxy-4-butanediamic acid" EXACT RESID-systematic []
-synonym: "(2S,3R)-3-hydroxyasparagine" EXACT RESID-name []
-synonym: "(3R)3HyAsn" EXACT PSI-MOD-label []
-synonym: "2-azanyl-3-hydroxy-4-butanediamic acid" EXACT RESID-alternate []
-synonym: "erythro-beta-hydroxylated L-asparagine" EXACT PSI-MOD-alternate []
-synonym: "L-erythro-beta-hydroxyasparagine" EXACT RESID-alternate []
-synonym: "MOD_RES (3R)-3-hydroxyasparagine" EXACT UniProt-feature []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 4 H 6 N 2 O 3" xsd:string
-property_value: MassAvg "130.10" xsd:float
-property_value: MassMono "130.037842" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0369
-is_a: MOD:01688
-
-[Term]
-id: MOD:00036
-name: (2S,3R)-3-hydroxyaspartic acid
-def: "A protein modification that effectively converts an L-aspartic acid residue to (2S,3R)-3-hydroxyaspartic acid." [OMSSA:59, PubMed:6572939, PubMed:6871167, PubMed:8355279, RESID:AA0027, Unimod:35#D, ChEBI:141848]
-subset: PSI-MOD-slim
-synonym: "(2S,3R)-2-amino-3-hydroxybutanedioic acid" EXACT RESID-systematic []
-synonym: "(2S,3R)-3-hydroxyaspartic acid" EXACT RESID-name []
-synonym: "(3R)3HyAsp" EXACT PSI-MOD-label []
-synonym: "2-amino-3-hydroxysuccinic acid" EXACT RESID-alternate []
-synonym: "2-azanyl-3-hydroxybutanedioic acid" EXACT RESID-alternate []
-synonym: "3-hydroxyaspartic acid" EXACT RESID-alternate []
-synonym: "erythro-beta-hydroxylated L-aspartic acid" EXACT PSI-MOD-alternate []
-synonym: "hydroxylationd" EXACT OMSSA-label []
-synonym: "L-erythro-beta-hydroxyaspartic acid" EXACT RESID-alternate []
-synonym: "MOD_RES (3R)-3-hydroxyaspartate" EXACT UniProt-feature []
-synonym: "Oxidation" RELATED PSI-MS-label []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 4 H 5 N 1 O 4" xsd:string
-property_value: MassAvg "131.09" xsd:float
-property_value: MassMono "131.021858" xsd:float
-property_value: Origin "D" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:35
-xref: uniprot.ptm:PTM-0371
-is_a: MOD:01926
-
-[Term]
-id: MOD:00037
-name: 5-hydroxy-L-lysine
-def: "A protein modification that effectively converts an L-lysine  residue to one of the diastereomeric 5-hydroxy-L-lysine  residues." [ChEBI:60175, PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "5-hydroxylated L-lysine" EXACT PSI-MOD-alternate []
-synonym: "5HyLys" EXACT PSI-MOD-label []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 6 H 12 N 2 O 2" xsd:string
-property_value: MassAvg "144.17" xsd:float
-property_value: MassMono "144.089878" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0044
-is_a: MOD:01047
-
-[Term]
-id: MOD:00038
-name: 3-hydroxy-L-proline
-def: "A protein modification that effectively converts an L-proline residue to 3-hydroxy-L-proline." [ChEBI:16889, PubMed:2400108, PubMed:3734192, PubMed:4343807, RESID:AA0029]
-subset: PSI-MOD-slim
-synonym: "(2S,3S)-3-hydroxypyrrolidine-2-carboxylic acid" EXACT RESID-systematic []
-synonym: "3-hydroxy-L-proline" EXACT RESID-name []
-synonym: "3-hydroxylated L-proline" EXACT PSI-MOD-alternate []
-synonym: "3-trans-hydroxy-L-proline" EXACT RESID-alternate []
-synonym: "3HyPro" EXACT PSI-MOD-label []
-synonym: "beta-hydroxypyrrolidine-alpha-carboxylic acid" EXACT RESID-alternate []
-synonym: "L-threo-3-hydroxyproline" EXACT RESID-alternate []
-synonym: "MOD_RES 3-hydroxyproline" EXACT UniProt-feature []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 5 H 7 N 1 O 2" xsd:string
-property_value: MassAvg "113.12" xsd:float
-property_value: MassMono "113.047678" xsd:float
-property_value: Origin "P" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0030
-is_a: MOD:01024
-
-[Term]
-id: MOD:00039
-name: 4-hydroxy-L-proline
-def: "A protein modification that effectively converts an L-proline residue to 4-hydroxy-L-proline" [ChEBI:18095, PubMed:11292863, PubMed:2400108, PubMed:3734192, RESID:AA0030]
-subset: PSI-MOD-slim
-synonym: "(2S,4R)-4-hydroxypyrrolidine-2-carboxylic acid" EXACT RESID-systematic []
-synonym: "4-hydroxy-L-proline" EXACT RESID-name []
-synonym: "4-hydroxylated L-proline" EXACT PSI-MOD-alternate []
-synonym: "4-hydroxyproline" EXACT RESID-alternate []
-synonym: "4-trans-hydroxy-L-proline" EXACT RESID-alternate []
-synonym: "4HyPro" EXACT PSI-MOD-label []
-synonym: "gamma-hydroxypyrrolidine-alpha-carboxylic acid" EXACT RESID-alternate []
-synonym: "L-threo-4-hydroxyproline" EXACT RESID-alternate []
-synonym: "MOD_RES 4-hydroxyproline" EXACT UniProt-feature []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 5 H 7 N 1 O 2" xsd:string
-property_value: MassAvg "113.12" xsd:float
-property_value: MassMono "113.047678" xsd:float
-property_value: Origin "P" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0043
-is_a: MOD:01024
-
-[Term]
-id: MOD:00040
-name: 2-pyrrolidone-5-carboxylic acid (Gln)
-def: "A protein modification that effectively converts an L-glutamine residue to 2-pyrrolidone-5-carboxylic acid." [ChEBI:30652, DeltaMass:123, OMSSA:110, PubMed:10214721, PubMed:1836357, PubMed:26343, PubMed:3473473, RESID:AA0031#GLN, Unimod:28#Q]
-comment: DeltaMass gives a formula C 5 H 5 N 1 O 2 with mass 111.1
-subset: PSI-MOD-slim
-synonym: "(2S)-5-oxo-2-pyrrolidinecarboxylic acid" EXACT RESID-systematic []
-synonym: "2-oxopyrrolidine-5-carboxylic acid" EXACT RESID-alternate []
-synonym: "2-pyrrolidone-5-carboxylic acid" EXACT RESID-name []
-synonym: "5-oxoproline" EXACT RESID-alternate []
-synonym: "5-oxopyrrolidine-2-carboxylic acid" EXACT RESID-alternate []
-synonym: "5-pyrrolidone-2-carboxylic acid" EXACT RESID-alternate []
-synonym: "Gln->pyro-Glu" RELATED PSI-MS-label []
-synonym: "MOD_RES Pyrrolidone carboxylic acid" EXACT UniProt-feature []
-synonym: "N-pyrrolidone carboxyl (N terminus)" EXACT DeltaMass-label []
-synonym: "ntermpeppyroq" EXACT OMSSA-label []
-synonym: "PCA" EXACT RESID-alternate []
-synonym: "PyrGlu(Gln)" EXACT PSI-MOD-label []
-synonym: "Pyro-glu from Q" RELATED Unimod-description []
-synonym: "pyroglutamic acid" EXACT RESID-alternate []
-synonym: "Pyroglutamic Acid formed from Gln" EXACT DeltaMass-label []
-synonym: "Pyroglutamyl" EXACT DeltaMass-label []
-property_value: DiffAvg "-17.03" xsd:float
-property_value: DiffFormula "C 0 H -3 N -1 O 0" xsd:string
-property_value: DiffMono "-17.026549" xsd:float
-property_value: Formula "C 5 H 6 N 1 O 2" xsd:string
-property_value: MassAvg "112.11" xsd:float
-property_value: MassMono "112.039853" xsd:float
-property_value: Origin "Q" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:28
-xref: uniprot.ptm:PTM-0261
-is_a: MOD:00907
-is_a: MOD:01048
-is_a: MOD:01160
-
-[Term]
-id: MOD:00041
-name: L-gamma-carboxyglutamic acid
-def: "A protein modification that effectively converts an L-glutamic acid residue to L-gamma-carboxyglutamic acid." [DeltaMass:217, OMSSA:48, PubMed:10517147, PubMed:1807167, PubMed:3263814, PubMed:4528109, PubMed:7457858, PubMed:8135347, PubMed:8868490, PubMed:9188685, RESID:AA0032, Unimod:299#E]
-comment: DeltaMass has an incorrect formula C 6 H 7 N 5 O 1 (N and O reversed) with mass 173.
-subset: PSI-MOD-slim
-synonym: "(3S)-3-aminopropane-1,1,3-tricarboxylic acid" EXACT RESID-systematic []
-synonym: "(3S)-3-azanylpropane-1,1,3-tricarboxylic acid" EXACT RESID-alternate []
-synonym: "1-carboxyglutamic acid" RELATED RESID-misnomer []
-synonym: "3-amino-1,1,3-propanetricarboxylic acid" EXACT RESID-alternate []
-synonym: "3-azanylpropane-1,1,3-tricarboxylic acid" EXACT RESID-alternate []
-synonym: "4-carboxyglutamic acid" EXACT RESID-alternate []
-synonym: "4CbxGlu" EXACT PSI-MOD-label []
-synonym: "Carboxy" RELATED PSI-MS-label []
-synonym: "Carboxy" RELATED Unimod-interim []
-synonym: "Carboxy Glutamyl" EXACT DeltaMass-label []
-synonym: "Carboxylation" RELATED Unimod-description []
-synonym: "gamma-carboxylated L-glutamic acid" EXACT PSI-MOD-alternate []
-synonym: "gammacarboxyle" EXACT OMSSA-label []
-synonym: "L-gamma-carboxyglutamic acid" EXACT RESID-name []
-synonym: "MOD_RES 4-carboxyglutamate" EXACT UniProt-feature []
-property_value: DiffAvg "44.01" xsd:float
-property_value: DiffFormula "C 1 H 0 N 0 O 2" xsd:string
-property_value: DiffMono "43.989829" xsd:float
-property_value: Formula "C 6 H 7 N 1 O 5" xsd:string
-property_value: MassAvg "173.12" xsd:float
-property_value: MassMono "173.032422" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:299
-xref: uniprot.ptm:PTM-0039
-is_a: MOD:00906
-is_a: MOD:01152
-
-[Term]
-id: MOD:00042
-name: L-aspartic 4-phosphoric anhydride
-def: "A protein modification that effectively converts an L-aspartic acid residue to L-aspartic 4-phosphoric anhydride." [ChEBI:15836, PubMed:4357737, RESID:AA0033, Unimod:21#D]
-synonym: "(2S)-2-amino-4-oxo-4-(phosphonooxy)butanoic acid" EXACT RESID-systematic []
-synonym: "2-aminobutanedioic 4-phosphoric anhydride" EXACT RESID-alternate []
-synonym: "2-azanyl-4-oxo-4-(phosphonooxy)butanoic acid" EXACT RESID-alternate []
-synonym: "4-oxo-O-phosphono-L-homoserine" EXACT RESID-alternate []
-synonym: "4-phosphoaspartic acid" EXACT RESID-alternate []
-synonym: "4-phosphorylated L-aspartatic acid" EXACT PSI-MOD-alternate []
-synonym: "ACT_SITE 4-aspartylphosphate intermediate" EXACT UniProt-feature []
-synonym: "beta-aspartyl phosphate" EXACT RESID-alternate []
-synonym: "L-aspartic 4-phosphoric anhydride" EXACT RESID-name []
-synonym: "MOD_RES 4-aspartylphosphate" EXACT UniProt-feature []
-synonym: "PAsp" EXACT PSI-MOD-label []
-synonym: "Phospho" RELATED PSI-MS-label []
-synonym: "Phosphorylation" RELATED Unimod-description []
-property_value: DiffAvg "79.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 0 O 3 P 1" xsd:string
-property_value: DiffMono "79.966331" xsd:float
-property_value: Formula "C 4 H 6 N 1 O 6 P 1" xsd:string
-property_value: MassAvg "195.07" xsd:float
-property_value: MassMono "194.993274" xsd:float
-property_value: Origin "D" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:21
-xref: uniprot.ptm:PTM-0038
-is_a: MOD:00904
-is_a: MOD:01455
-
-[Term]
-id: MOD:00043
-name: S-phospho-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-phospho-L-cysteine." [PubMed:3142516, PubMed:7961745, PubMed:8128219, RESID:AA0034, Unimod:21#C]
-synonym: "(2R)-2-amino-3-(phosphonosulfanyl)propanoic acid" EXACT RESID-systematic []
-synonym: "2-azanyl-3-(phosphonosulfanyl)propanoic acid" EXACT RESID-alternate []
-synonym: "ACT_SITE Phosphocysteine intermediate" EXACT UniProt-feature []
-synonym: "cysteine phosphate thioester" EXACT RESID-alternate []
-synonym: "MOD_RES Phosphocysteine" EXACT UniProt-feature []
-synonym: "PCys" EXACT PSI-MOD-label []
-synonym: "Phospho" RELATED PSI-MS-label []
-synonym: "Phosphorylation" RELATED Unimod-description []
-synonym: "S-phospho-L-cysteine" EXACT RESID-name []
-synonym: "S-phosphonocysteine" EXACT RESID-alternate []
-synonym: "S-phosphorylated L-cysteine" EXACT PSI-MOD-alternate []
-synonym: "S3-phosphocysteine" EXACT RESID-alternate []
-property_value: DiffAvg "79.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 0 O 3 P 1 S 0" xsd:string
-property_value: DiffMono "79.966331" xsd:float
-property_value: Formula "C 3 H 6 N 1 O 4 P 1 S 1" xsd:string
-property_value: MassAvg "183.12" xsd:float
-property_value: MassMono "182.975515" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:21
-xref: uniprot.ptm:PTM-0251
-is_a: MOD:00696
-is_a: MOD:00777
-is_a: MOD:00905
-
-[Term]
-id: MOD:00044
-name: 1'-phospho-L-histidine
-def: "A protein modification that effectively converts an L-histidine residue to tele-phospho-L-histidine (N-tau-phospho-L-histidine, 1'-phospho-L-histidine)." [PubMed:11038361, PubMed:5642389, PubMed:6692818, RESID:AA0035]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-(1-phosphono-1H-imidazol-4-yl)propanoic acid" EXACT RESID-systematic []
-synonym: "1'-phospho-L-histidine" EXACT RESID-name []
-synonym: "2-azanyl-3-(1-phosphono-1H-imidazol-4-yl)propanoic acid" EXACT RESID-alternate []
-synonym: "ACT_SITE Tele-phosphohistidine intermediate" EXACT UniProt-feature []
-synonym: "histidine-3-phosphate" RELATED RESID-misnomer []
-synonym: "histidine-N(epsilon)-phosphate" EXACT RESID-alternate []
-synonym: "histidine-N1'-phosphate" EXACT RESID-alternate []
-synonym: "MOD_RES Tele-phosphohistidine" EXACT UniProt-feature []
-synonym: "N(tau)-phosphohistidine" EXACT RESID-alternate []
-synonym: "N1-phosphonohistidine" EXACT RESID-alternate []
-synonym: "NE2-phosphonohistidine" EXACT RESID-alternate []
-synonym: "Ntau-phosphorylated L-histidine" EXACT PSI-MOD-alternate []
-synonym: "NtPHis" EXACT PSI-MOD-label []
-synonym: "Phospho" RELATED PSI-MS-label []
-synonym: "Phosphorylation" RELATED Unimod-description []
-synonym: "tele-phosphohistidine" EXACT RESID-alternate []
-property_value: DiffAvg "79.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 0 O 3 P 1" xsd:string
-property_value: DiffMono "79.966331" xsd:float
-property_value: Formula "C 6 H 8 N 3 O 4 P 1" xsd:string
-property_value: MassAvg "217.12" xsd:float
-property_value: MassMono "217.025242" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0325
-is_a: MOD:00890
-
-[Term]
-id: MOD:00045
-name: 3'-phospho-L-histidine
-def: "A protein modification that effectively converts an L-histidine residue to pros-phospho-L-histidine (N-pi-phospho-L-histidine, 3'-phospho-L-histidine)." [PubMed:1549615, PubMed:5642389, PubMed:6692818, PubMed:7669763, PubMed:7803390, RESID:AA0036]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-(3-phosphono-3H-imidazol-4-yl)propanoic acid" EXACT RESID-systematic []
-synonym: "2-azanyl-3-(3-phosphono-3H-imidazol-4-yl)propanoic acid" EXACT RESID-alternate []
-synonym: "3'-phospho-L-histidine" EXACT RESID-name []
-synonym: "ACT_SITE Pros-phosphohistidine intermediate" EXACT UniProt-feature []
-synonym: "histidine-1-phosphate" RELATED RESID-misnomer []
-synonym: "histidine-N(delta)-phosphate" EXACT RESID-alternate []
-synonym: "histidine-N3'-phosphate" EXACT RESID-alternate []
-synonym: "MOD_RES Pros-phosphohistidine" EXACT UniProt-feature []
-synonym: "N(pi)-phosphohistidine" EXACT RESID-alternate []
-synonym: "N3-phosphonohistidine" EXACT RESID-alternate []
-synonym: "ND1-phosphonohistidine" EXACT RESID-alternate []
-synonym: "Npi-phosphorylated L-histidine" EXACT PSI-MOD-alternate []
-synonym: "NpPHis" EXACT PSI-MOD-label []
-synonym: "Phospho" RELATED PSI-MS-label []
-synonym: "Phosphorylation" RELATED Unimod-description []
-synonym: "pros-phosphohistidine" EXACT RESID-alternate []
-property_value: DiffAvg "79.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 0 O 3 P 1" xsd:string
-property_value: DiffMono "79.966331" xsd:float
-property_value: Formula "C 6 H 8 N 3 O 4 P 1" xsd:string
-property_value: MassAvg "217.12" xsd:float
-property_value: MassMono "217.025242" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0260
-is_a: MOD:00890
-
-[Term]
-id: MOD:00046
-name: O-phospho-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O-phospho-L-serine." [ChEBI:15811, DeltaMass:0, OMSSA:6, PubMed:12923550, PubMed:4065410, PubMed:8061611, RESID:AA0037, Unimod:21#S]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-(phosphonooxy)propanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-3-hydroxypropanoic acid 3-phosphate" EXACT RESID-alternate []
-synonym: "2-azanyl-3-(phosphonooxy)propanoic acid" EXACT RESID-alternate []
-synonym: "ACT_SITE Phosphoserine intermediate" EXACT UniProt-feature []
-synonym: "MOD_RES Phosphoserine" EXACT UniProt-feature []
-synonym: "O-phospho-L-serine" EXACT RESID-name []
-synonym: "O-phosphonoserine" EXACT RESID-alternate []
-synonym: "O-phosphorylated L-serine" EXACT PSI-MOD-alternate []
-synonym: "O3-phosphoserine" EXACT RESID-alternate []
-synonym: "OPSer" EXACT PSI-MOD-label []
-synonym: "Phospho" RELATED PSI-MS-label []
-synonym: "Phospho Seryl" EXACT DeltaMass-label []
-synonym: "Phosphorylation" RELATED Unimod-description []
-synonym: "phosphorylations" EXACT OMSSA-label []
-synonym: "serine phosphate ester" EXACT RESID-alternate []
-property_value: DiffAvg "79.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 0 O 3 P 1" xsd:string
-property_value: DiffMono "79.966331" xsd:float
-property_value: Formula "C 3 H 6 N 1 O 5 P 1" xsd:string
-property_value: MassAvg "167.06" xsd:float
-property_value: MassMono "166.998359" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:21
-xref: uniprot.ptm:PTM-0253
-is_a: MOD:00771
-is_a: MOD:00916
-is_a: MOD:01455
-
-[Term]
-id: MOD:00047
-name: O-phospho-L-threonine
-def: "A protein modification that effectively converts an L-threonine residue to O-phospho-L-threonine." [ChEBI:21967, DeltaMass:0, OMSSA:7, PubMed:12923550, PubMed:7678926, RESID:AA0038, Unimod:21#T]
-subset: PSI-MOD-slim
-synonym: "(2S,3R)-2-amino-3-(phosphonooxy)butanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-3-hydroxybutanoic acid 3-phosphate" EXACT RESID-alternate []
-synonym: "2-azanyl-3-(phosphonooxy)butanoic acid" EXACT RESID-alternate []
-synonym: "MOD_RES Phosphothreonine" EXACT UniProt-feature []
-synonym: "O-phospho-L-threonine" EXACT RESID-name []
-synonym: "O-phosphorylated L-threonine" EXACT PSI-MOD-alternate []
-synonym: "O3-phosphothreonine" EXACT RESID-alternate []
-synonym: "OPThr" EXACT PSI-MOD-label []
-synonym: "Phospho" RELATED PSI-MS-label []
-synonym: "Phospho Threonyl" EXACT DeltaMass-label []
-synonym: "Phosphorylation" RELATED Unimod-description []
-synonym: "phosphorylationt" EXACT OMSSA-label []
-synonym: "threonine phosphate ester" EXACT RESID-alternate []
-property_value: DiffAvg "79.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 0 O 3 P 1" xsd:string
-property_value: DiffMono "79.966331" xsd:float
-property_value: Formula "C 4 H 8 N 1 O 5 P 1" xsd:string
-property_value: MassAvg "181.08" xsd:float
-property_value: MassMono "181.014009" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:21
-xref: uniprot.ptm:PTM-0254
-is_a: MOD:00773
-is_a: MOD:00917
-is_a: MOD:01455
-
-[Term]
-id: MOD:00048
-name: O4'-phospho-L-tyrosine
-def: "A protein modification that effectively converts an L-tyrosine residue to O4'-phospho-L-tyrosine." [DeltaMass:0, OMSSA:8, PubMed:10226369, PubMed:1725475, RESID:AA0039, Unimod:21#Y]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-(4-phosphonooxyphenyl)propanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-3-(4-hydroxyphenyl)propanoic acid 4'-phosphate" EXACT RESID-alternate []
-synonym: "2-azanyl-3-(4-phosphonooxyphenyl)propanoic acid" EXACT RESID-alternate []
-synonym: "MOD_RES Phosphotyrosine" EXACT UniProt-feature []
-synonym: "O4'-phospho-L-tyrosine" EXACT RESID-name []
-synonym: "O4'-phosphorylated L-tyrosine" EXACT PSI-MOD-alternate []
-synonym: "O4-phosphotyrosine" EXACT RESID-alternate []
-synonym: "OPTyr" EXACT PSI-MOD-label []
-synonym: "Phospho" RELATED PSI-MS-label []
-synonym: "Phospho Tyrosinyl" EXACT DeltaMass-label []
-synonym: "Phosphorylation" RELATED Unimod-description []
-synonym: "phosphorylationy" EXACT OMSSA-label []
-synonym: "tyrosine phosphate" EXACT RESID-alternate []
-property_value: DiffAvg "79.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 0 O 3 P 1" xsd:string
-property_value: DiffMono "79.966331" xsd:float
-property_value: Formula "C 9 H 10 N 1 O 5 P 1" xsd:string
-property_value: MassAvg "243.15" xsd:float
-property_value: MassMono "243.029659" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:21
-xref: uniprot.ptm:PTM-0255
-is_a: MOD:00774
-is_a: MOD:00919
-is_a: MOD:01455
-
-[Term]
-id: MOD:00049
-name: 2'-[3-carboxamido-3-(trimethylammonio)propyl]-L-histidine
-def: "A protein modification that effectively converts an L-histidine residue to diphthamide." [ChEBI:16692, DeltaMass:122, PubMed:15316019, PubMed:7430147, RESID:AA0040, Unimod:375#H]
-synonym: "(2R)-1-amino-4-(4-[(2S)-2-amino-2-carboxyethyl]-1H-imidazol-2-yl)-N,N,N-trimethyl-1-oxobutan-2-aminium" EXACT RESID-systematic []
-synonym: "(3-[4-(2-amino-2-carboxy-ethyl)-1H-imidazol-2-yl]-1-carbamoyl-propyl)-trimethylammonium" EXACT RESID-alternate []
-synonym: "1-azanyl-4-(4-[2-azanyl-2-carboxyethyl]-1H-imidazol-2-yl)-N,N,N-trimethyl-1-oxobutan-2-azanium" EXACT RESID-alternate []
-synonym: "2'-[3-carboxamido-3-(trimethylammonio)propyl]-L-histidine" EXACT RESID-name []
-synonym: "2-[(R)-3-carboxamido-3-(trimethylammonio)propyl]-4-((S)-2-amino-2-carboxyethyl)-1H-imidazole" EXACT RESID-alternate []
-synonym: "2-[3-carboxamido-3-(trimethylammonio)propyl]histidine" EXACT RESID-alternate []
-synonym: "2-amino-3-[[2-(3-amino-3-carbamoyl-prop-1-enyl)-1,1,3-trimethyl-2,3-dihydroimidazol-5-yl]]propanoic acid" EXACT RESID-alternate []
-synonym: "2-amino-4-[[5-(2-amino-2-carboxylato-ethyl)-1,1,3-trimethyl-2,3-dihydroimidazol-2-yl]]but-3-enamide" EXACT RESID-alternate []
-synonym: "alpha-(aminocarbonyl)-4-(2-amino-2-carboxyethyl)-N,N,N-trimethyl-1H-imidazole-2-propanaminium" EXACT RESID-alternate []
-synonym: "Diphth" EXACT PSI-MOD-label []
-synonym: "Diphthamide" RELATED PSI-MS-label []
-synonym: "Diphthamide" RELATED Unimod-description []
-synonym: "diphthamide" EXACT RESID-alternate []
-synonym: "diphthamide (from histidine)" EXACT DeltaMass-label []
-synonym: "MOD_RES Diphthamide" EXACT UniProt-feature []
-property_value: DiffAvg "143.21" xsd:float
-property_value: DiffFormula "C 7 H 15 N 2 O 1" xsd:string
-property_value: DiffMono "143.117890" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 13 H 22 N 5 O 2" xsd:string
-property_value: MassAvg "280.35" xsd:float
-property_value: MassMono "280.176801" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:375
-xref: uniprot.ptm:PTM-0118
-is_a: MOD:00909
-
-[Term]
-id: MOD:00050
-name: N-acetyl-L-alanine
-def: "A protein modification that effectively converts an L-alanine residue to N-acetyl-L-alanine." [PubMed:363452, PubMed:4700463, RESID:AA0041]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-(acetamido)propanoic acid" EXACT RESID-systematic []
-synonym: "2-(acetylamino)propanoic acid" EXACT RESID-alternate []
-synonym: "2-(acetylazanyl)propanoic acid" EXACT RESID-alternate []
-synonym: "AcAla" EXACT PSI-MOD-label []
-synonym: "acetylalanine" EXACT RESID-alternate []
-synonym: "MOD_RES N-acetylalanine" EXACT UniProt-feature []
-synonym: "N-acetyl-L-alanine" EXACT RESID-name []
-synonym: "N-acetylated L-alanine" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 2 H 2 N 0 O 1" xsd:string
-property_value: DiffMono "42.010565" xsd:float
-property_value: Formula "C 5 H 8 N 1 O 2" xsd:string
-property_value: MassAvg "114.12" xsd:float
-property_value: MassMono "114.055504" xsd:float
-property_value: Origin "A" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0199
-is_a: MOD:00901
-is_a: MOD:01458
-
-[Term]
-id: MOD:00051
-name: N-acetyl-L-aspartic acid
-def: "A protein modification that effectively converts an L-aspartic acid residue to N-acetyl-L-aspartic acid." [ChEBI:21547, PubMed:1560020, PubMed:2395459, RESID:AA0042]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-(acetamido)butanedioic acid" EXACT RESID-systematic []
-synonym: "2-(acetylamino)butanedioic acid" EXACT RESID-alternate []
-synonym: "2-(acetylazanyl)butanedioic acid" EXACT RESID-alternate []
-synonym: "AcAsp" EXACT PSI-MOD-label []
-synonym: "acetylaspartic acid" EXACT RESID-alternate []
-synonym: "MOD_RES N-acetylaspartate" EXACT UniProt-feature []
-synonym: "N-acetyl-L-aspartic acid" EXACT RESID-name []
-synonym: "N-acetylated L-aspartic acid" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 2 H 2 N 0 O 1" xsd:string
-property_value: DiffMono "42.010565" xsd:float
-property_value: Formula "C 6 H 8 N 1 O 4" xsd:string
-property_value: MassAvg "158.13" xsd:float
-property_value: MassMono "158.045333" xsd:float
-property_value: Origin "D" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0200
-is_a: MOD:00904
-is_a: MOD:01458
-
-[Term]
-id: MOD:00052
-name: N-acetyl-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to N-acetyl-L-cysteine." [ChEBI:28939, PubMed:11857757, PubMed:11999733, PubMed:12175151, PubMed:14730666, PubMed:1500421, PubMed:15350136, PubMed:6725286, RESID:AA0043]
-comment: incidental to RESID:AA0223
-subset: PSI-MOD-slim
-synonym: "(2R)-2-acetamido-3-sulfanylpropanoic acid" EXACT RESID-systematic []
-synonym: "2-acetylamino-3-mercaptopropanoic acid" EXACT RESID-alternate []
-synonym: "2-acetylamino-3-sulfanylpropanoic acid" EXACT RESID-alternate []
-synonym: "2-acetylazanyl-3-sulfanylpropanoic acid" EXACT RESID-alternate []
-synonym: "Acetyl" RELATED PSI-MS-label []
-synonym: "MOD_RES N-acetylcysteine" EXACT UniProt-feature []
-synonym: "N-acetyl-L-cysteine" EXACT RESID-name []
-synonym: "N-acetylated cysteine" EXACT PSI-MOD-alternate []
-synonym: "N-acetylcysteine" EXACT RESID-alternate []
-synonym: "NAcCys" EXACT PSI-MOD-label []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 2 H 2 N 0 O 1 S 0" xsd:string
-property_value: DiffMono "42.010565" xsd:float
-property_value: Formula "C 5 H 8 N 1 O 2 S 1" xsd:string
-property_value: MassAvg "146.18" xsd:float
-property_value: MassMono "146.027574" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0201
-is_a: MOD:00646
-is_a: MOD:01458
-
-[Term]
-id: MOD:00053
-name: N-acetyl-L-glutamic acid
-def: "A protein modification that effectively converts an L-glutamic acid residue to N-acetyl-L-glutamic acid." [ChEBI:17533, PubMed:6725286, RESID:AA0044]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-(acetamido)pentanedioic acid" EXACT RESID-systematic []
-synonym: "2-(acetylamino)pentanedioic acid" EXACT RESID-alternate []
-synonym: "2-(acetylazanyl)pentanedioic acid" EXACT RESID-alternate []
-synonym: "acetylglutamic acid" EXACT RESID-alternate []
-synonym: "AcGlu" EXACT PSI-MOD-label []
-synonym: "MOD_RES N-acetylglutamate" EXACT UniProt-feature []
-synonym: "N-acetyl-L-glutamic acid" EXACT RESID-name []
-synonym: "N-acetylated L-glutamic acid" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 2 H 2 N 0 O 1" xsd:string
-property_value: DiffMono "42.010565" xsd:float
-property_value: Formula "C 7 H 10 N 1 O 4" xsd:string
-property_value: MassAvg "172.16" xsd:float
-property_value: MassMono "172.060983" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0202
-is_a: MOD:00906
-is_a: MOD:01458
-
-[Term]
-id: MOD:00054
-name: N-acetyl-L-glutamine
-def: "A protein modification that effectively converts an L-glutamine residue to N-acetyl-L-glutamine." [RESID:AA0045]
-comment: This is a deprecated entry in RESID. It probably does not occur naturally [JSG].
-synonym: "(2S)-2-acetamido-5-pentanediamic acid" EXACT RESID-systematic []
-synonym: "2-acetylamino-5-amino-5-oxopentanoic acid" EXACT RESID-alternate []
-synonym: "2-acetylamino-5-pentanediamic acid" EXACT RESID-alternate []
-synonym: "2-acetylazanyl-5-azanyl-5-oxopentanoic acid" EXACT RESID-alternate []
-synonym: "acetylglutamine" EXACT RESID-alternate []
-synonym: "AcGln" EXACT PSI-MOD-label []
-synonym: "N-acetyl-L-glutamine" EXACT RESID-name []
-synonym: "N-acetylated L-glutamine" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 2 H 2 N 0 O 1" xsd:string
-property_value: DiffMono "42.010565" xsd:float
-property_value: Formula "C 7 H 11 N 2 O 3" xsd:string
-property_value: MassAvg "171.18" xsd:float
-property_value: MassMono "171.076967" xsd:float
-property_value: Origin "Q" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00907
-is_a: MOD:01458
-
-[Term]
-id: MOD:00055
-name: N-acetylglycine
-def: "A protein modification that effectively converts a glycine residue to N-acetylglycine." [PubMed:272676, PubMed:5545094, PubMed:6754709, RESID:AA0046]
-subset: PSI-MOD-slim
-synonym: "(acetylamino)acetic acid" EXACT RESID-alternate []
-synonym: "(acetylazanyl)ethanoic acid" EXACT RESID-alternate []
-synonym: "2-(acetamido)ethanoic acid" EXACT RESID-systematic []
-synonym: "2-(acetylamino)ethanoic acid" EXACT RESID-alternate []
-synonym: "aceturic acid" EXACT RESID-alternate []
-synonym: "AcGly" EXACT PSI-MOD-label []
-synonym: "MOD_RES N-acetylglycine" EXACT UniProt-feature []
-synonym: "N-acetylated glycine" EXACT PSI-MOD-alternate []
-synonym: "N-acetylglycine" EXACT RESID-name []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 2 H 2 N 0 O 1" xsd:string
-property_value: DiffMono "42.010565" xsd:float
-property_value: Formula "C 4 H 6 N 1 O 2" xsd:string
-property_value: MassAvg "100.10" xsd:float
-property_value: MassMono "100.039853" xsd:float
-property_value: Origin "G" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0203
-is_a: MOD:00908
-is_a: MOD:01458
-
-[Term]
-id: MOD:00056
-name: N-acetyl-L-isoleucine
-def: "A protein modification that effectively converts an L-isoleucine residue to N-acetyl-L-isoleucine." [PubMed:8034631, RESID:AA0047]
-comment: This is a deprecated entry in RESID. It probably does not occur naturally [JSG].
-synonym: "(2S,3S)-2-acetamido-3-methylpentanoic acid" EXACT RESID-systematic []
-synonym: "2-acetylamino-3-methylpentanoic acid" EXACT RESID-alternate []
-synonym: "2-acetylazanyl-3-methylpentanoic acid" EXACT RESID-alternate []
-synonym: "acetylisoleucine" EXACT RESID-alternate []
-synonym: "AcIle" EXACT PSI-MOD-label []
-synonym: "N-acetyl-L-isoleucine" EXACT RESID-name []
-synonym: "N-acetylated L-isoleucine" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 2 H 2 N 0 O 1" xsd:string
-property_value: DiffMono "42.010565" xsd:float
-property_value: Formula "C 8 H 14 N 1 O 2" xsd:string
-property_value: MassAvg "156.20" xsd:float
-property_value: MassMono "156.102454" xsd:float
-property_value: Origin "I" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0204
-is_a: MOD:00910
-is_a: MOD:01458
-
-[Term]
-id: MOD:00057
-name: N2-acetyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N2-acetyl-L-lysine." [PubMed:11857757, PubMed:11999733, PubMed:12175151, PubMed:14730666, PubMed:15350136, RESID:AA0048]
-comment: This is a deprecated entry in RESID. It probably does not occur naturally [JSG].
-synonym: "(2S)-2-acetamido-6-aminohexanoic acid" EXACT RESID-systematic []
-synonym: "2-acetylamino-6-aminohexanoic acid" EXACT RESID-alternate []
-synonym: "2-acetylazanyl-6-azanylhexanoic acid" EXACT RESID-alternate []
-synonym: "Acetyl" RELATED PSI-MS-label []
-synonym: "N2-acetyl-L-lysine" EXACT RESID-name []
-synonym: "N2-acetylated L-lysine" EXACT PSI-MOD-alternate []
-synonym: "N2-acetyllysine" EXACT RESID-alternate []
-synonym: "N2AcLys" EXACT PSI-MOD-label []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 2 H 2 N 0 O 1" xsd:string
-property_value: DiffMono "42.010565" xsd:float
-property_value: Formula "C 8 H 15 N 2 O 2" xsd:string
-property_value: MassAvg "171.22" xsd:float
-property_value: MassMono "171.113353" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00723
-is_a: MOD:01458
-
-[Term]
-id: MOD:00058
-name: N-acetyl-L-methionine
-def: "A protein modification that effectively converts an L-methionine to N-acetyl-L-methionine." [PubMed:7944406, RESID:AA0049]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-acetamido-4-(methylsulfanyl)butanoic acid" EXACT RESID-systematic []
-synonym: "2-acetylamino-4-(methylsulfanyl)butanoic acid" EXACT RESID-alternate []
-synonym: "2-acetylamino-4-(methylthio)butanoic acid" EXACT RESID-alternate []
-synonym: "2-acetylazanyl-4-(methylsulfanyl)butanoic acid" EXACT RESID-alternate []
-synonym: "acetylmethionine" EXACT RESID-alternate []
-synonym: "AcMet" EXACT PSI-MOD-label []
-synonym: "methionamine" EXACT RESID-alternate []
-synonym: "MOD_RES N-acetylmethionine" EXACT UniProt-feature []
-synonym: "N-acetyl-L-methionine" EXACT RESID-name []
-synonym: "N-acetylated L-methionine" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 2 H 2 N 0 O 1 S 0" xsd:string
-property_value: DiffMono "42.010565" xsd:float
-property_value: Formula "C 7 H 12 N 1 O 2 S 1" xsd:string
-property_value: MassAvg "174.24" xsd:float
-property_value: MassMono "174.058875" xsd:float
-property_value: Origin "M" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0205
-is_a: MOD:00913
-is_a: MOD:01458
-
-[Term]
-id: MOD:00059
-name: N-acetyl-L-proline
-def: "A protein modification that effectively converts an L-proline residue to N-acetyl-L-proline." [PubMed:2928307, RESID:AA0050]
-subset: PSI-MOD-slim
-synonym: "(2S)-1-acetyl-2-pyrrolidinecarboxylic acid" EXACT RESID-systematic []
-synonym: "1-acetylproline" EXACT RESID-alternate []
-synonym: "acetylproline" EXACT RESID-alternate []
-synonym: "MOD_RES N-acetylproline" EXACT UniProt-feature []
-synonym: "N-acetyl-L-proline" EXACT RESID-name []
-synonym: "N-acetylated L-proline" EXACT PSI-MOD-alternate []
-synonym: "N-acetylproline" EXACT RESID-alternate []
-synonym: "NAcPro" EXACT PSI-MOD-label []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 2 H 2 N 0 O 1" xsd:string
-property_value: DiffMono "42.010565" xsd:float
-property_value: Formula "C 7 H 10 N 1 O 2" xsd:string
-property_value: MassAvg "140.16" xsd:float
-property_value: MassMono "140.071154" xsd:float
-property_value: Origin "P" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0206
-is_a: MOD:00915
-is_a: MOD:01458
-
-[Term]
-id: MOD:00060
-name: N-acetyl-L-serine
-def: "A protein modification that effectively converts an L-serine residue to N-acetyl-L-serine." [PubMed:11857757, PubMed:11999733, PubMed:12175151, PubMed:14730666, PubMed:15350136, PubMed:1880797, PubMed:2106685, PubMed:6997045, RESID:AA0051]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-acetamido-3-hydroxypropanoic acid" EXACT RESID-systematic []
-synonym: "2-acetylamino-3-hydroxypropanoic acid" EXACT RESID-alternate []
-synonym: "2-acetylazanyl-3-hydroxypropanoic acid" EXACT RESID-alternate []
-synonym: "Acetyl" RELATED PSI-MS-label []
-synonym: "MOD_RES N-acetylserine" EXACT UniProt-feature []
-synonym: "N-acetyl-L-serine" EXACT RESID-name []
-synonym: "N-acetylated L-serine" EXACT PSI-MOD-alternate []
-synonym: "N-acetylserine" EXACT RESID-alternate []
-synonym: "NAcSer" EXACT PSI-MOD-label []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 2 H 2 N 0 O 1" xsd:string
-property_value: DiffMono "42.010565" xsd:float
-property_value: Formula "C 5 H 8 N 1 O 3" xsd:string
-property_value: MassAvg "130.12" xsd:float
-property_value: MassMono "130.050418" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0207
-is_a: MOD:00647
-is_a: MOD:01458
-
-[Term]
-id: MOD:00061
-name: N-acetyl-L-threonine
-def: "A protein modification that effectively converts an L-threonine residue to N-acetyl-L-threonine." [PubMed:11857757, PubMed:11999733, PubMed:12175151, PubMed:14730666, PubMed:15350136, PubMed:2106685, PubMed:6997045, RESID:AA0052]
-subset: PSI-MOD-slim
-synonym: "(2S,3R)-2-acetamido-3-hydroxybutanoic acid" EXACT RESID-systematic []
-synonym: "2-acetylamino-3-hydroxybutanoic acid" EXACT RESID-alternate []
-synonym: "2-acetylazanyl-3-hydroxybutanoic acid" EXACT RESID-alternate []
-synonym: "Acetyl" RELATED PSI-MS-label []
-synonym: "Acetylation" RELATED Unimod-description []
-synonym: "MOD_RES N-acetylthreonine" EXACT UniProt-feature []
-synonym: "N-acetyl-L-threonine" EXACT RESID-name []
-synonym: "N-acetylated L-threonine" EXACT PSI-MOD-alternate []
-synonym: "N-acetylthreonine" EXACT RESID-alternate []
-synonym: "N-methylcarbonylthreonine" EXACT RESID-alternate []
-synonym: "NAcThr" EXACT PSI-MOD-label []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 2 H 2 N 0 O 1" xsd:string
-property_value: DiffMono "42.010565" xsd:float
-property_value: Formula "C 6 H 10 N 1 O 3" xsd:string
-property_value: MassAvg "144.15" xsd:float
-property_value: MassMono "144.066068" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0208
-is_a: MOD:01186
-is_a: MOD:01458
-
-[Term]
-id: MOD:00062
-name: N-acetyl-L-tyrosine
-def: "A protein modification that effectively converts an L-tyrosine residue to N-acetyl-L-tyrosine." [PubMed:11857757, PubMed:11999733, PubMed:12175151, PubMed:14730666, PubMed:15350136, PubMed:2506074, PubMed:475783, RESID:AA0053]
-synonym: "(2S)-2-acetamido-3-(4-hydoxyphenyl)propanoic acid" EXACT RESID-systematic []
-synonym: "2-acetylamino-3-(4-hydoxyphenyl)propanoic acid" EXACT RESID-alternate []
-synonym: "2-acetylazanyl-3-(4-hydoxyphenyl)propanoic acid" EXACT RESID-alternate []
-synonym: "Acetyl" RELATED PSI-MS-label []
-synonym: "AcTyr" EXACT PSI-MOD-label []
-synonym: "MOD_RES N-acetyltyrosine" EXACT UniProt-feature []
-synonym: "N-acetyl-L-tyrosine" EXACT RESID-name []
-synonym: "N-acetylated L-tyrosine" EXACT PSI-MOD-alternate []
-synonym: "N-acetyltyrosine" EXACT RESID-alternate []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 2 H 2 N 0 O 1" xsd:string
-property_value: DiffMono "42.010565" xsd:float
-property_value: Formula "C 11 H 12 N 1 O 3" xsd:string
-property_value: MassAvg "206.22" xsd:float
-property_value: MassMono "206.081718" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0209
-is_a: MOD:00919
-is_a: MOD:01458
-
-[Term]
-id: MOD:00063
-name: N-acetyl-L-valine
-def: "A protein modification that effectively converts an L-valine residue to N-acetyl-L-valine." [PubMed:1735421, RESID:AA0054]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-acetamido-3-methylbutanoic acid" EXACT RESID-systematic []
-synonym: "2-acetylamino-3-methylbutanoic acid" EXACT RESID-alternate []
-synonym: "2-acetylazanyl-3-methylbutanoic acid" EXACT RESID-alternate []
-synonym: "AcVal" EXACT PSI-MOD-label []
-synonym: "MOD_RES N-acetylvaline" EXACT UniProt-feature []
-synonym: "N-acetyl-L-valine" EXACT RESID-name []
-synonym: "N-acetylated L-valine" EXACT PSI-MOD-alternate []
-synonym: "N-acetylvaline" EXACT RESID-alternate []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 2 H 2 N 0 O 1" xsd:string
-property_value: DiffMono "42.010565" xsd:float
-property_value: Formula "C 7 H 12 N 1 O 2" xsd:string
-property_value: MassAvg "142.18" xsd:float
-property_value: MassMono "142.086804" xsd:float
-property_value: Origin "V" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0210
-is_a: MOD:00920
-is_a: MOD:01458
-
-[Term]
-id: MOD:00064
-name: N6-acetyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-acetyl-L-lysine." [ChEBI:17752, DeltaMass:214, OMSSA:24, PubMed:11369851, PubMed:11857757, PubMed:11999733, PubMed:12175151, PubMed:14730666, PubMed:15350136, PubMed:1680872, PubMed:670159, RESID:AA0055, Unimod:1#K]
-subset: PSI-MOD-slim
-synonym: "(2S)-6-acetamido-2-aminohexanoic acid" EXACT RESID-systematic []
-synonym: "6-acetylamino-2-aminohexanoic acid" EXACT RESID-alternate []
-synonym: "6-acetylazanyl-2-aminohexanoic acid" EXACT RESID-alternate []
-synonym: "Acetyl" RELATED PSI-MS-label []
-synonym: "Acetylation" RELATED Unimod-description []
-synonym: "acetylk" EXACT OMSSA-label []
-synonym: "epsilon-acetyllysine" EXACT RESID-alternate []
-synonym: "MOD_RES N6-acetyllysine" EXACT UniProt-feature []
-synonym: "N(zeta)-acetyllysine" EXACT RESID-alternate []
-synonym: "N6-acetyl-L-lysine" EXACT RESID-name []
-synonym: "N6-acetylated L-lysine" EXACT PSI-MOD-alternate []
-synonym: "N6AcLys" EXACT PSI-MOD-label []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 2 H 2 N 0 O 1" xsd:string
-property_value: DiffMono "42.010565" xsd:float
-property_value: Formula "C 8 H 14 N 2 O 2" xsd:string
-property_value: MassAvg "170.21" xsd:float
-property_value: MassMono "170.105528" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:1
-xref: uniprot.ptm:PTM-0190
-is_a: MOD:00723
-is_a: MOD:01875
-
-[Term]
-id: MOD:00065
-name: S-acetyl-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-acetyl-L-cysteine." [PubMed:11857757, PubMed:11999733, PubMed:12175151, PubMed:1310545, PubMed:14730666, PubMed:15350136, RESID:AA0056, Unimod:1#C]
-subset: PSI-MOD-slim
-synonym: "(2R)-3-acetylsulfanyl-2-aminopropanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-3-(acetylthio)propanoic acid" EXACT RESID-alternate []
-synonym: "2-azanyl-3-(acetylsulfanyl)propanoic acid" EXACT RESID-alternate []
-synonym: "Acetyl" RELATED PSI-MS-label []
-synonym: "Acetylation" RELATED Unimod-description []
-synonym: "ACT_SITE S-acetylcysteine intermediate" EXACT UniProt-feature []
-synonym: "cysteine acetate thioester" EXACT RESID-alternate []
-synonym: "S-acetyl-L-cysteine" EXACT RESID-name []
-synonym: "S-acetylcysteine" EXACT RESID-alternate []
-synonym: "SAcCys" EXACT PSI-MOD-label []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 2 H 2 N 0 O 1 S 0" xsd:string
-property_value: DiffMono "42.010565" xsd:float
-property_value: Formula "C 5 H 7 N 1 O 2 S 1" xsd:string
-property_value: MassAvg "145.18" xsd:float
-property_value: MassMono "145.019749" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:1
-is_a: MOD:00645
-is_a: MOD:00646
-
-[Term]
-id: MOD:00066
-name: N-formylglycine
-def: "A protein modification that effectively converts a glycine residue to N-formylglycine." [PubMed:5139483, RESID:AA0057]
-synonym: "(formylamino)acetic acid" EXACT RESID-alternate []
-synonym: "(formylamino)ethanoic acid" EXACT RESID-systematic []
-synonym: "(formylazanyl)ethanoic acid" EXACT RESID-alternate []
-synonym: "2-formamidoacetic acid" EXACT RESID-alternate []
-synonym: "2-formamidoethanoic acid" EXACT RESID-alternate []
-synonym: "MOD_RES N-formylglycine" EXACT UniProt-feature []
-synonym: "N(alpha)-formylglycine" EXACT RESID-alternate []
-synonym: "N-formylated glycine" EXACT PSI-MOD-alternate []
-synonym: "N-formylglycine" EXACT RESID-name []
-synonym: "NFoGly" EXACT PSI-MOD-label []
-property_value: DiffAvg "28.01" xsd:float
-property_value: DiffFormula "C 1 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "27.994915" xsd:float
-property_value: Formula "C 3 H 4 N 1 O 2" xsd:string
-property_value: MassAvg "86.07" xsd:float
-property_value: MassMono "86.024203" xsd:float
-property_value: Origin "G" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0211
-is_a: MOD:00409
-is_a: MOD:00908
-is_a: MOD:01696
-
-[Term]
-id: MOD:00067
-name: N-D-glucuronoylglycine
-def: "A protein modification that effectively converts a glycine residue to N-D-glucuronoylglycine." [OMSSA:50, PubMed:10858503, PubMed:12716131, PubMed:6493057, PubMed:7398618, RESID:AA0058]
-synonym: "2-(glucuronoylamino)ethanoic acid" EXACT RESID-systematic []
-synonym: "Glucuronyl" RELATED PSI-MS-label []
-synonym: "MOD_RES N-D-glucuronoyl glycine" EXACT UniProt-feature []
-synonym: "N-D-glucuronoyl-glycine" EXACT RESID-name []
-synonym: "N-D-glucuronyl-glycine" EXACT RESID-alternate []
-synonym: "NGlcAGly" EXACT PSI-MOD-label []
-synonym: "ntermpepglucuronylg" EXACT OMSSA-label []
-property_value: DiffAvg "176.12" xsd:float
-property_value: DiffFormula "C 6 H 8 N 0 O 6" xsd:string
-property_value: DiffMono "176.032088" xsd:float
-property_value: Formula "C 8 H 12 N 1 O 7" xsd:string
-property_value: MassAvg "234.18" xsd:float
-property_value: MassMono "234.061377" xsd:float
-property_value: Origin "G" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0331
-is_a: MOD:00447
-is_a: MOD:00908
-
-[Term]
-id: MOD:00068
-name: N-myristoylglycine
-def: "A protein modification that effectively converts a glycine residue to N-myristoylglycine." [OMSSA:80, PubMed:11955007, PubMed:11955008, PubMed:1326520, PubMed:1386601, PubMed:6436247, PubMed:7543369, RESID:AA0059, Unimod:45#G]
-subset: PSI-MOD-slim
-synonym: "(tetradecanoylamino)ethanoic acid" EXACT RESID-systematic []
-synonym: "LIPID N-myristoyl glycine" EXACT UniProt-feature []
-synonym: "Myristoyl" RELATED PSI-MS-label []
-synonym: "Myristoylation" RELATED Unimod-description []
-synonym: "N-(1-oxotetradecyl)glycine" EXACT RESID-alternate []
-synonym: "N-(C14:0 aliphatic acyl)glycine" EXACT PSI-MOD-alternate []
-synonym: "N-myristoyl-glycine" EXACT RESID-name []
-synonym: "N-myristoylated glycine" EXACT PSI-MOD-alternate []
-synonym: "N-myristylglycine" EXACT RESID-alternate []
-synonym: "N-tetradecanoylglycine" EXACT RESID-alternate []
-synonym: "NMyrGly" EXACT PSI-MOD-label []
-synonym: "ntermpepmyristoylationg" EXACT OMSSA-label []
-property_value: DiffAvg "210.36" xsd:float
-property_value: DiffFormula "C 14 H 26 N 0 O 1" xsd:string
-property_value: DiffMono "210.198365" xsd:float
-property_value: Formula "C 16 H 30 N 1 O 2" xsd:string
-property_value: MassAvg "268.42" xsd:float
-property_value: MassMono "268.227654" xsd:float
-property_value: Origin "G" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:45
-xref: uniprot.ptm:PTM-0221
-is_a: MOD:00650
-is_a: MOD:00908
-is_a: MOD:01696
-
-[Term]
-id: MOD:00069
-name: N-palmitoyl-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to N-palmitoyl-L-cysteine." [PubMed:10896212, PubMed:4575979, PubMed:9056182, PubMed:9593755, RESID:AA0060]
-comment: incidental to RESID:AA0107 incidental to RESID:AA0309
-subset: PSI-MOD-slim
-synonym: "(2R)-2-hexadecanoylamino-3-sulfanylpropanoic acid" EXACT RESID-systematic []
-synonym: "2-hexadecanamido-3-sulfanylpropanoic acid" EXACT RESID-alternate []
-synonym: "2-hexadecanoylamino-3-mercaptopropanoic acid" EXACT RESID-alternate []
-synonym: "LIPID N-palmitoyl cysteine" EXACT UniProt-feature []
-synonym: "N-(1-oxahexadecyl)-L-cysteine" EXACT RESID-alternate []
-synonym: "N-palmitoyl-L-cysteine" EXACT RESID-name []
-synonym: "N-palmitoylated L-cysteine" EXACT PSI-MOD-alternate []
-synonym: "N-hexadecanoylated L-cysteine" EXACT PSI-MOD-alternate []
-synonym: "NPamCys" EXACT PSI-MOD-label []
-synonym: "Palmitoyl" RELATED PSI-MS-label []
-synonym: "Palmitoylation" RELATED Unimod-description []
-property_value: DiffAvg "238.41" xsd:float
-property_value: DiffFormula "C 16 H 30 N 0 O 1 S 0" xsd:string
-property_value: DiffMono "238.229666" xsd:float
-property_value: Formula "C 19 H 36 N 1 O 2 S 1" xsd:string
-property_value: MassAvg "342.56" xsd:float
-property_value: MassMono "342.246675" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0222
-is_a: MOD:01684
-is_a: MOD:01685
-
-[Term]
-id: MOD:00070
-name: N-methyl-L-alanine
-def: "A protein modification that effectively converts an L-alanine residue to N-methyl-L-alanine." [ChEBI:17519, PubMed:323502, PubMed:337304, PubMed:7007074, RESID:AA0061]
-comment: Polypeptides with monomethylated amino terminals can undergo premature cleavage during the coupling step of an Edman degradation. This can result in \"preview\" with both a residue and the following residue being seen from the first step on through a sequence [JSG].
-subset: PSI-MOD-slim
-synonym: "(2S)-2-methylaminopropanoic acid" EXACT RESID-systematic []
-synonym: "2-methylazanylpropanoic acid" EXACT RESID-alternate []
-synonym: "Methyl" RELATED PSI-MS-label []
-synonym: "Methylation" RELATED Unimod-description []
-synonym: "MOD_RES N-methylalanine" EXACT UniProt-feature []
-synonym: "N-methyl-L-alanine" EXACT RESID-name []
-synonym: "N-methylalanine" EXACT RESID-alternate []
-synonym: "N-methylated L-alanine" EXACT PSI-MOD-alternate []
-synonym: "NMe1Ala" EXACT PSI-MOD-label []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 4 H 7 N 1 O 1" xsd:string
-property_value: MassAvg "85.11" xsd:float
-property_value: MassMono "85.052764" xsd:float
-property_value: Origin "A" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0214
-is_a: MOD:01461
-is_a: MOD:01680
-
-[Term]
-id: MOD:00071
-name: N,N,N-trimethyl-L-alanine
-def: "A protein modification that effectively converts an L-alanine residue to N,N,N-trimethyl-L-alanine." [PubMed:12590383, PubMed:332162, PubMed:3979397, PubMed:6778808, PubMed:7715456, RESID:AA0062]
-subset: PSI-MOD-slim
-synonym: "(1S)-1-carboxy-N,N,N-trimethylethanaminium" EXACT RESID-systematic []
-synonym: "(1S)-1-carboxy-N,N,N-trimethylethanazanium" EXACT RESID-alternate []
-synonym: "(2S)-2-(trimethylammonio)propanoic acid" EXACT RESID-alternate []
-synonym: "MOD_RES N,N,N-trimethylalanine" EXACT UniProt-feature []
-synonym: "N,N,N-trimethyl-L-alanine" EXACT RESID-name []
-synonym: "N,N,N-trimethylalanine cation" EXACT RESID-alternate []
-synonym: "N,N,N-trimethylalaninium" EXACT RESID-alternate []
-synonym: "N,N,N-trimethylated L-alanine" EXACT PSI-MOD-alternate []
-synonym: "N2Me3+Ala" EXACT PSI-MOD-label []
-synonym: "NMe3Ala" EXACT PSI-MOD-label []
-synonym: "tri-Methylation" RELATED Unimod-description []
-synonym: "Trimethyl" RELATED PSI-MS-label []
-property_value: DiffAvg "43.09" xsd:float
-property_value: DiffFormula "C 3 H 7 N 0 O 0" xsd:string
-property_value: DiffMono "43.054227" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 6 H 13 N 1 O 1" xsd:string
-property_value: MassAvg "115.18" xsd:float
-property_value: MassMono "115.099165" xsd:float
-property_value: Origin "A" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0177
-is_a: MOD:01461
-is_a: MOD:01698
-
-[Term]
-id: MOD:00072
-name: N-methylglycine
-def: "A protein modification that effectively converts a glycine residue to N-methylglycine." [ChEBI:15611, DeltaMass:0, PubMed:1593629, RESID:AA0063]
-comment: DeltaMass also has an entry for the free amino acid. Polypeptides with monomethylated amino terminals can undergo premature cleavage during the coupling step of an Edman degradation. This can result in \"preview\" with both a residue and the following residue being seen from the first step on through a sequence [JSG].
-synonym: "L-sarcosine" EXACT RESID-alternate []
-synonym: "Methyl" RELATED PSI-MS-label []
-synonym: "methylaminoacetic acid" EXACT RESID-alternate []
-synonym: "methylaminoethanoic acid" EXACT RESID-systematic []
-synonym: "Methylation" RELATED Unimod-description []
-synonym: "N-methylated glycine" EXACT PSI-MOD-alternate []
-synonym: "N-methylglycine" EXACT RESID-name []
-synonym: "NMe1Gly" EXACT PSI-MOD-label []
-synonym: "Sar" EXACT DeltaMass-label []
-synonym: "Sarcosine" EXACT DeltaMass-label []
-synonym: "Sarcosyl" EXACT DeltaMass-label []
-synonym: "MOD_RES N-methylglycine" EXACT UniProt-feature []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 3 H 5 N 1 O 1" xsd:string
-property_value: MassAvg "71.08" xsd:float
-property_value: MassMono "71.037114" xsd:float
-property_value: Origin "G" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0483
-is_a: MOD:00570
-is_a: MOD:00714
-is_a: MOD:01680
-
-[Term]
-id: MOD:00073
-name: N-methyl-L-methionine
-def: "A protein modification that effectively converts an L-methionine residue to N-methyl-L-methionine." [DeltaMass:169, PubMed:323502, PubMed:3298225, RESID:AA0064]
-comment: Polypeptides with monomethylated amino terminals can undergo premature cleavage during the coupling step of an Edman degradation. This can result in \"preview\" with both a residue and the following residue being seen from the first step on through a sequence [JSG].
-subset: PSI-MOD-slim
-synonym: "(2S)-2-methylamino-4-(methylsulfanyl)butanoic acid" EXACT RESID-systematic []
-synonym: "2-methylamino-4-(methylthio)butanoic acid" EXACT RESID-alternate []
-synonym: "Methyl" RELATED PSI-MS-label []
-synonym: "Methyl Methionyl" EXACT DeltaMass-label []
-synonym: "Methylation" RELATED Unimod-description []
-synonym: "MOD_RES N-methylmethionine" EXACT UniProt-feature []
-synonym: "N-methyl-L-methionine" EXACT RESID-name []
-synonym: "N-methylated L-methionine" EXACT PSI-MOD-alternate []
-synonym: "N-methylmethionine" EXACT RESID-alternate []
-synonym: "NMe1Met" EXACT PSI-MOD-label []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 6 H 11 N 1 O 1 S 1" xsd:string
-property_value: MassAvg "145.22" xsd:float
-property_value: MassMono "145.056135" xsd:float
-property_value: Origin "M" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0217
-is_a: MOD:01463
-is_a: MOD:01680
-
-[Term]
-id: MOD:00074
-name: N-methyl-L-phenylalanine
-def: "A protein modification that effectively converts an L-phenylalanine residue to N-methyl-L-phenylalanine." [PubMed:2577730, PubMed:413571, RESID:AA0065]
-comment: Polypeptides with monomethylated amino terminals can undergo premature cleavage during the coupling step of an Edman degradation. This can result in \"preview\" with both a residue and the following residue being seen from the first step on through a sequence [JSG].
-subset: PSI-MOD-slim
-synonym: "(2S)-2-methylamino-3-phenylpropanoic acid" EXACT RESID-systematic []
-synonym: "Methyl" RELATED PSI-MS-label []
-synonym: "Methylation" RELATED Unimod-description []
-synonym: "MOD_RES N-methylphenylalanine" EXACT UniProt-feature []
-synonym: "N-methyl-L-phenylalanine" EXACT RESID-name []
-synonym: "N-methylated L-phenylalanine" EXACT PSI-MOD-alternate []
-synonym: "N-methylphenylalanine" EXACT RESID-alternate []
-synonym: "NMe1Phe" EXACT PSI-MOD-label []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 10 H 11 N 1 O 1" xsd:string
-property_value: MassAvg "161.20" xsd:float
-property_value: MassMono "161.084064" xsd:float
-property_value: Origin "F" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0218
-is_a: MOD:01063
-is_a: MOD:01680
-
-[Term]
-id: MOD:00075
-name: N,N-dimethyl-L-proline
-def: "A protein modification that effectively converts an L-proline residue to N,N-dimethyl-L-proline." [ChEBI:21451, PubMed:12964758, PubMed:14570711, PubMed:193025, PubMed:3882426, PubMed:6254758, RESID:AA0066, Unimod:529]
-comment: Unimod terminal specification corrected [JSG].
-subset: PSI-MOD-slim
-synonym: "(2S)-2-carboxy-1,1-dimethylpyrrolidinium" EXACT RESID-systematic []
-synonym: "1,1-dimethyl-L-prolinium" EXACT RESID-alternate []
-synonym: "Delta:H(5)C(2)" RELATED Unimod-interim []
-synonym: "Dimethyl" RELATED PSI-MS-label []
-synonym: "Dimethylation of proline residue" RELATED Unimod-description []
-synonym: "MOD_RES N,N-dimethylproline" EXACT UniProt-feature []
-synonym: "N,N-dimethyl-L-proline" EXACT RESID-name []
-synonym: "N,N-dimethyl-L-prolinium" EXACT RESID-alternate []
-synonym: "N,N-dimethylated L-proline" EXACT PSI-MOD-alternate []
-synonym: "NMe2Pro" EXACT PSI-MOD-label []
-synonym: "stachydrin" EXACT RESID-alternate []
-property_value: DiffAvg "29.06" xsd:float
-property_value: DiffFormula "C 2 H 5 N 0 O 0" xsd:string
-property_value: DiffMono "29.038577" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 7 H 13 N 1 O 1" xsd:string
-property_value: MassAvg "127.19" xsd:float
-property_value: MassMono "127.099165" xsd:float
-property_value: Origin "P" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:529
-xref: uniprot.ptm:PTM-0179
-is_a: MOD:00710
-is_a: MOD:01462
-
-[Term]
-id: MOD:00076
-name: symmetric dimethyl-L-arginine
-def: "A protein modification that effectively converts an L-arginine residue to symmetric dimethylarginine, N(omega),N'(omega)-dimethyl-L-arginine." [PubMed:12964758, PubMed:14570711, PubMed:15835918, PubMed:2426402, PubMed:5128665, RESID:AA0067, Unimod:36#R]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-5-[((methylamino)(methylimino)methyl)amino]pentanoic acid" EXACT RESID-systematic []
-synonym: "di-Methylation" RELATED Unimod-description []
-synonym: "Dimethyl" RELATED PSI-MS-label []
-synonym: "MOD_RES Omega-N-methylated arginine" EXACT UniProt-feature []
-synonym: "MOD_RES Symmetric dimethylarginine" EXACT UniProt-feature []
-synonym: "N3,N4-dimethylarginine" EXACT RESID-alternate []
-synonym: "N5-[(methylamino)(methylimino)methyl]ornithine" EXACT RESID-alternate []
-synonym: "NG,N'G-dimethylarginine" EXACT RESID-alternate []
-synonym: "NoNo'Me2Arg" EXACT PSI-MOD-label []
-synonym: "omega-N,omega-N'-dimethyl-L-arginine" EXACT RESID-name []
-synonym: "omega-N,omega-N'-dimethylated L-arginine" EXACT PSI-MOD-alternate []
-synonym: "symmetric dimethylarginine" EXACT RESID-alternate []
-property_value: DiffAvg "28.05" xsd:float
-property_value: DiffFormula "C 2 H 4 N 0 O 0" xsd:string
-property_value: DiffMono "28.031300" xsd:float
-property_value: Formula "C 8 H 16 N 4 O 1" xsd:string
-property_value: MassAvg "184.24" xsd:float
-property_value: MassMono "184.132411" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:36
-xref: uniprot.ptm:PTM-0287
-is_a: MOD:00602
-is_a: MOD:00783
-
-[Term]
-id: MOD:00077
-name: asymmetric dimethyl-L-arginine
-def: "A protein modification that effectively converts an L-arginine residue to asymmetric dimethylarginine, N(omega),N(omega)-dimethyl-L-arginine." [ChEBI:17929, PubMed:11152131, PubMed:12964758, PubMed:14570711, PubMed:15835918, PubMed:3032834, RESID:AA0068, Unimod:36#R]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-5-([(dimethylamino)(imino)methyl]amino)pentanoic acid" EXACT RESID-systematic []
-synonym: "asymmetric dimethylarginine" EXACT RESID-alternate []
-synonym: "di-Methylation" RELATED Unimod-description []
-synonym: "Dimethyl" RELATED PSI-MS-label []
-synonym: "MOD_RES Asymmetric dimethylarginine" EXACT UniProt-feature []
-synonym: "MOD_RES Omega-N-methylated arginine" EXACT UniProt-feature []
-synonym: "N5-[(dimethylamino)(imino)methyl]ornithine" EXACT RESID-alternate []
-synonym: "NG,NG-dimethylarginine" EXACT RESID-alternate []
-synonym: "NoNoMe2Arg" EXACT PSI-MOD-label []
-synonym: "omega-N,omega-N-dimethlyated L-arginine" EXACT PSI-MOD-alternate []
-synonym: "omega-N,omega-N-dimethyl-L-arginine" EXACT RESID-name []
-property_value: DiffAvg "28.05" xsd:float
-property_value: DiffFormula "C 2 H 4 N 0 O 0" xsd:string
-property_value: DiffMono "28.031300" xsd:float
-property_value: Formula "C 8 H 16 N 4 O 1" xsd:string
-property_value: MassAvg "184.24" xsd:float
-property_value: MassMono "184.132411" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:36
-xref: uniprot.ptm:PTM-0066
-is_a: MOD:00602
-is_a: MOD:00783
-
-[Term]
-id: MOD:00078
-name: omega-N-methyl-L-arginine
-def: "A protein modification that effectively converts an L-arginine residue to N(omega)-methyl-L-arginine." [PubMed:11875433, PubMed:15835918, PubMed:2426402, PubMed:5128665, RESID:AA0069]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-5-[(imino(methylamino)methyl)amino]pentanoic acid" EXACT RESID-systematic []
-synonym: "Methyl" RELATED PSI-MS-label []
-synonym: "Methylation" RELATED Unimod-description []
-synonym: "MOD_RES Omega-N-methylarginine" EXACT UniProt-feature []
-synonym: "MOD_RES Omega-N-methylated arginine" EXACT UniProt-feature []
-synonym: "NG-methylarginine" EXACT RESID-alternate []
-synonym: "NoMeArg" EXACT PSI-MOD-label []
-synonym: "omega-N-methyl-L-arginine" EXACT RESID-name []
-synonym: "omega-N-methylated L-arginine" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 7 H 14 N 4 O 1" xsd:string
-property_value: MassAvg "170.22" xsd:float
-property_value: MassMono "170.116761" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0237
-is_a: MOD:00414
-is_a: MOD:00602
-
-[Term]
-id: MOD:00079
-name: N4-methyl-L-asparagine
-def: "A protein modification that effectively converts an L-asparagine residue to N4-methyl-L-asparagine." [OMSSA:75, PubMed:11875433, PubMed:2356973, PubMed:3782095, RESID:AA0070, Unimod:34#N]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-N4-methylbutanediamic acid" EXACT RESID-systematic []
-synonym: "beta-aspartyl methylamide" EXACT RESID-alternate []
-synonym: "beta-methylasparagine" RELATED RESID-misnomer []
-synonym: "Methyl" RELATED PSI-MS-label []
-synonym: "Methylation" RELATED Unimod-description []
-synonym: "methyln" EXACT OMSSA-label []
-synonym: "MOD_RES N4-methylasparagine" EXACT UniProt-feature []
-synonym: "N(gamma)-methylasparagine" EXACT RESID-alternate []
-synonym: "N-methylasparagine" EXACT RESID-alternate []
-synonym: "N4-methyl-L-asparagine" EXACT RESID-name []
-synonym: "N4-methylated L-asparagine" EXACT PSI-MOD-alternate []
-synonym: "N4Me1Asn" EXACT PSI-MOD-label []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 5 H 8 N 2 O 2" xsd:string
-property_value: MassAvg "128.13" xsd:float
-property_value: MassMono "128.058578" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:34
-xref: uniprot.ptm:PTM-0183
-is_a: MOD:00599
-is_a: MOD:00602
-is_a: MOD:00673
-is_a: MOD:00894
-
-[Term]
-id: MOD:00080
-name: N5-methyl-L-glutamine
-def: "A protein modification that effectively converts an L-glutamine residue to N5-methyl-L-glutamine." [ChEBI:17592, DeltaMass:166, PubMed:11118225, PubMed:11875433, PubMed:365579, RESID:AA0071]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-5-methylamino-5-oxopentanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-N5-methylpentanediamic acid" EXACT RESID-alternate []
-synonym: "gamma-methylglutamine" EXACT RESID-alternate []
-synonym: "Methyl" RELATED PSI-MS-label []
-synonym: "Methylation" RELATED Unimod-description []
-synonym: "MOD_RES N5-methylglutamine" EXACT UniProt-feature []
-synonym: "N(delta)-methylglutamine" EXACT RESID-alternate []
-synonym: "N-methylglutamine" EXACT RESID-alternate []
-synonym: "N5-methyl-L-glutamine" EXACT RESID-name []
-synonym: "N5-methylated L-glutamine" EXACT PSI-MOD-alternate []
-synonym: "N5Me1Gln" EXACT PSI-MOD-label []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 6 H 10 N 2 O 2" xsd:string
-property_value: MassAvg "142.16" xsd:float
-property_value: MassMono "142.074228" xsd:float
-property_value: Origin "Q" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0185
-is_a: MOD:00602
-is_a: MOD:00722
-
-[Term]
-id: MOD:00081
-name: L-glutamic acid 5-methyl ester (Glu)
-def: "A protein modification that effectively converts an L-glutamic acid residue to L-glutamate 5-methyl ester." [DeltaMass:167, OMSSA:17, OMSSA:70, PubMed:16888, PubMed:6300110, RESID:AA0072#GLU, Unimod:34#E]
-comment: DeltaMass gives the formula \"C 6 H 9 O 1 N 3\" with mass 143 (formula incorrect, N and O reversed) [JSG].
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-5-methoxy-5-oxopentanoic acid" EXACT RESID-systematic []
-synonym: "(5)-methyl L-hydrogen glutamate" EXACT RESID-alternate []
-synonym: "2-aminopentanedioic acid 5-methyl ester" EXACT RESID-alternate []
-synonym: "5-methyl esterified L-glutamic acid" EXACT PSI-MOD-alternate []
-synonym: "5-methyl L-2-aminoglutarate" EXACT RESID-alternate []
-synonym: "5-methyl L-glutamate" EXACT RESID-alternate []
-synonym: "glutamic acid 5-methyl ester" EXACT RESID-alternate []
-synonym: "glutamic acid gamma-methyl ester" EXACT RESID-alternate []
-synonym: "L-glutamic acid 5-methyl ester" EXACT RESID-name []
-synonym: "meestere" EXACT OMSSA-label []
-synonym: "Methyl" RELATED PSI-MS-label []
-synonym: "methyl ester" RELATED Unimod-alternate []
-synonym: "Methylation" RELATED Unimod-description []
-synonym: "methyle" EXACT OMSSA-label []
-synonym: "MOD_RES Glutamate methyl ester (Glu)" EXACT UniProt-feature []
-synonym: "O-methyl Glutamyl" EXACT DeltaMass-label []
-synonym: "O5MeGlu" EXACT PSI-MOD-label []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 6 H 9 N 1 O 3" xsd:string
-property_value: MassAvg "143.14" xsd:float
-property_value: MassMono "143.058243" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:34
-xref: uniprot.ptm:PTM-0128
-is_a: MOD:01453
-
-[Term]
-id: MOD:00082
-name: 3'-methyl-L-histidine
-def: "A protein modification that effectively converts an L-histidine residue to pros-methyl-L-histidine (N-pi-methyl-L-histidine, 3'-methyl-L-histidine)." [PubMed:10660523, PubMed:11875433, PubMed:3467365, PubMed:6692818, PubMed:8076, PubMed:8645219, RESID:AA0073]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-(3-methyl-3H-imidazol-4-yl)propanoic acid" EXACT RESID-systematic []
-synonym: "1-methylhistidine" RELATED RESID-misnomer []
-synonym: "3'-methyl-L-histidine" EXACT RESID-name []
-synonym: "Methyl" RELATED PSI-MS-label []
-synonym: "Methylation" RELATED Unimod-description []
-synonym: "MOD_RES Pros-methylhistidine" EXACT UniProt-feature []
-synonym: "N(delta)-methylhistidine" EXACT RESID-alternate []
-synonym: "N(pi)-methylhistidine" EXACT RESID-alternate []
-synonym: "NpMeHis" EXACT PSI-MOD-label []
-synonym: "pros-methylated L-histidine" EXACT PSI-MOD-alternate []
-synonym: "pros-methylhistidine" EXACT RESID-alternate []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 7 H 9 N 3 O 1" xsd:string
-property_value: MassAvg "151.17" xsd:float
-property_value: MassMono "151.074562" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0259
-is_a: MOD:02038
-is_a: MOD:00724
-
-[Term]
-id: MOD:00083
-name: N6,N6,N6-trimethyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6,N6,N6-trimethyl-L-lysine." [ChEBI:17311, PubMed:12590383, PubMed:3145979, PubMed:4304194, PubMed:6778808, PubMed:7093227, PubMed:8453381, RESID:AA0074]
-comment: DeltaMass calculates the mass difference from protonated lysine rather than neutral lysine; for trimethylated lysine starting from protonated lysine see MOD:00855
-subset: PSI-MOD-slim
-synonym: "(5S)-5-amino-5-carboxy-N,N,N-trimethylpentan-1-aminium" EXACT RESID-systematic []
-synonym: "2-amino-6-(trimethylammonio)hexanoic acid" EXACT RESID-alternate []
-synonym: "5-azanyl-5-carboxy-N,N,N-trimethylpentanazanium" EXACT RESID-alternate []
-synonym: "epsilon-trimethyllysine" EXACT RESID-alternate []
-synonym: "MOD_RES N6,N6,N6-trimethyllysine" EXACT UniProt-feature []
-synonym: "N(zeta)-trimethyllysine" EXACT RESID-alternate []
-synonym: "N-trimethylation (of lysine)" EXACT DeltaMass-label []
-synonym: "N6,N6,N6-trimethyl-L-lysine" EXACT RESID-name []
-synonym: "N6,N6,N6-trimethylated L-lysine" EXACT PSI-MOD-alternate []
-synonym: "N6,N6,N6-trimethyllysin-N6-ium" EXACT RESID-alternate []
-synonym: "N6,N6,N6-trimethyllysine cation" EXACT RESID-alternate []
-synonym: "N6Me3+Lys" EXACT PSI-MOD-label []
-synonym: "tri-Methylation" RELATED Unimod-description []
-synonym: "Trimethyl" RELATED PSI-MS-label []
-property_value: DiffAvg "43.09" xsd:float
-property_value: DiffFormula "C 3 H 7 N 0 O 0" xsd:string
-property_value: DiffMono "43.054227" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 9 H 19 N 2 O 1" xsd:string
-property_value: MassAvg "171.26" xsd:float
-property_value: MassMono "171.149190" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0187
-is_a: MOD:00602
-is_a: MOD:00663
-is_a: MOD:00711
-
-[Term]
-id: MOD:00084
-name: N6,N6-dimethyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6,N6-dimethyl-L-lysine." [OMSSA:36, PubMed:10550045, PubMed:12964758, PubMed:14570711, PubMed:3100523, PubMed:8453381, RESID:AA0075, Unimod:36#K]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-6-(dimethylamino)hexanoic acid" EXACT RESID-systematic []
-synonym: "di-Methylation" RELATED Unimod-description []
-synonym: "Dimethyl" RELATED PSI-MS-label []
-synonym: "dimethylk" EXACT OMSSA-label []
-synonym: "epsilon-dimethyllysine" EXACT RESID-alternate []
-synonym: "lysine derivative Lys(y)" EXACT RESID-alternate []
-synonym: "MOD_RES N6,N6-dimethyllysine" EXACT UniProt-feature []
-synonym: "N(zeta)-dimethyllysine" EXACT RESID-alternate []
-synonym: "N6,N6-dimethyl-L-lysine" EXACT RESID-name []
-synonym: "N6,N6-dimethylated L-lysine" EXACT PSI-MOD-alternate []
-synonym: "N6Me2Lys" EXACT PSI-MOD-label []
-property_value: DiffAvg "28.05" xsd:float
-property_value: DiffFormula "C 2 H 4 N 0 O 0" xsd:string
-property_value: DiffMono "28.031300" xsd:float
-property_value: Formula "C 8 H 16 N 2 O 1" xsd:string
-property_value: MassAvg "156.23" xsd:float
-property_value: MassMono "156.126263" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:36
-xref: uniprot.ptm:PTM-0188
-is_a: MOD:00429
-is_a: MOD:00602
-is_a: MOD:00663
-
-[Term]
-id: MOD:00085
-name: N6-methyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-methyl-L-lysine." [ChEBI:17604, DeltaMass:165, PubMed:11875433, PubMed:3926756, RESID:AA0076, Unimod:34#K]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-6-methylaminohexanoic acid" EXACT RESID-systematic []
-synonym: "epsilon-methyllysine" EXACT RESID-alternate []
-synonym: "Methyl" RELATED PSI-MS-label []
-synonym: "Methylation" RELATED Unimod-description []
-synonym: "MOD_RES N6-methyllysine" EXACT UniProt-feature []
-synonym: "N(zeta)-methyllysine" EXACT RESID-alternate []
-synonym: "N-methyl Lysyl" EXACT DeltaMass-label []
-synonym: "N6-methyl-L-lysine" EXACT RESID-name []
-synonym: "N6-methylated L-lysine" EXACT PSI-MOD-alternate []
-synonym: "N6Me1Lys" EXACT PSI-MOD-label []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 7 H 14 N 2 O 1" xsd:string
-property_value: MassAvg "142.20" xsd:float
-property_value: MassMono "142.110613" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:34
-xref: uniprot.ptm:PTM-0194
-is_a: MOD:00602
-is_a: MOD:01683
-
-[Term]
-id: MOD:00086
-name: N6-palmitoyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-palmitoyl-L-lysine." [OMSSA:93, PubMed:2498336, PubMed:7801126, PubMed:7939682, RESID:AA0077, Unimod:47#K]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-6-(hexadecanoylamino)hexanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-6-(hexadecanamido)hexanoic acid" EXACT RESID-alternate []
-synonym: "epsilon-palmitoyllysine" EXACT RESID-alternate []
-synonym: "LIPID N6-palmitoyl lysine" EXACT UniProt-feature []
-synonym: "N(zeta)-palmitoyllysine" EXACT RESID-alternate []
-synonym: "N6-(1-oxohexadecyl)-L-lysine" EXACT RESID-alternate []
-synonym: "N6-palmitoyl-L-lysine" EXACT RESID-name []
-synonym: "N6-palmitoylated L-lysine" EXACT PSI-MOD-alternate []
-synonym: "N6-hexadecanoylated L-lysine" EXACT PSI-MOD-alternate []
-synonym: "N6PamLys" EXACT PSI-MOD-label []
-synonym: "Palmitoyl" RELATED PSI-MS-label []
-synonym: "Palmitoylation" RELATED Unimod-description []
-synonym: "palmitoylationk" EXACT OMSSA-label []
-property_value: DiffAvg "238.41" xsd:float
-property_value: DiffFormula "C 16 H 30 N 0 O 1" xsd:string
-property_value: DiffMono "238.229666" xsd:float
-property_value: Formula "C 22 H 42 N 2 O 2" xsd:string
-property_value: MassAvg "366.59" xsd:float
-property_value: MassMono "366.324629" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:47
-xref: uniprot.ptm:PTM-0197
-is_a: MOD:00651
-is_a: MOD:01875
-
-[Term]
-id: MOD:00087
-name: N6-myristoyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-myristoyl-L-lysine." [OMSSA:81, PubMed:1402651, PubMed:8346241, RESID:AA0078, Unimod:45#K]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-6-(tetradecanoylamino)hexanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-6-(tetradecanamido)hexanoic acid" EXACT RESID-alternate []
-synonym: "epsilon-myristoyllysine" EXACT RESID-alternate []
-synonym: "LIPID N6-myristoyl lysine" EXACT UniProt-feature []
-synonym: "Myristoyl" RELATED PSI-MS-label []
-synonym: "Myristoylation" RELATED Unimod-description []
-synonym: "myristoylationk" EXACT OMSSA-label []
-synonym: "N(zeta)-myristoyllysine" EXACT RESID-alternate []
-synonym: "N6-(1-oxotetradecyl)-L-lysine" EXACT RESID-alternate []
-synonym: "N6-(C14:0 aliphatic acyl)lysine" EXACT PSI-MOD-alternate []
-synonym: "N6-myristoyl-L-lysine" EXACT RESID-name []
-synonym: "N6-myristoylated L-lysine" EXACT PSI-MOD-alternate []
-synonym: "N6MyrLys" EXACT PSI-MOD-label []
-property_value: DiffAvg "210.36" xsd:float
-property_value: DiffFormula "C 14 H 26 N 0 O 1" xsd:string
-property_value: DiffMono "210.198365" xsd:float
-property_value: Formula "C 20 H 38 N 2 O 2" xsd:string
-property_value: MassAvg "338.54" xsd:float
-property_value: MassMono "338.293328" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:45
-xref: uniprot.ptm:PTM-0196
-is_a: MOD:00650
-is_a: MOD:01875
-
-[Term]
-id: MOD:00088
-name: O-palmitoyl-L-threonine
-def: "A protein modification that effectively converts an L-threonine residue to O-palmitoyl-L-threonine." [OMSSA:95, PubMed:6642431, PubMed:8413602, RESID:AA0079, Unimod:47#T]
-subset: PSI-MOD-slim
-synonym: "(2S,3R)-2-amino-3-(hexadecanoyloxy)butanoic acid" EXACT RESID-systematic []
-synonym: "L-threonine hexadecanoate ester" EXACT RESID-alternate []
-synonym: "LIPID O-palmitoyl threonine" EXACT UniProt-feature []
-synonym: "O-palmitoyl-L-threonine" EXACT RESID-name []
-synonym: "O-palmitoylated L-threonine" EXACT PSI-MOD-alternate []
-synonym: "O-hexadecanoylated L-threonine" EXACT PSI-MOD-alternate []
-synonym: "O3-palmitoyl-threonine" EXACT RESID-alternate []
-synonym: "OPamThr" EXACT PSI-MOD-label []
-synonym: "Palmitoyl" RELATED PSI-MS-label []
-synonym: "Palmitoylation" RELATED Unimod-description []
-synonym: "palmitoylationt" EXACT OMSSA-label []
-synonym: "threonine palmitate ester" EXACT RESID-alternate []
-property_value: DiffAvg "238.41" xsd:float
-property_value: DiffFormula "C 16 H 30 N 0 O 1" xsd:string
-property_value: DiffMono "238.229666" xsd:float
-property_value: Formula "C 20 H 37 N 1 O 3" xsd:string
-property_value: MassAvg "339.52" xsd:float
-property_value: MassMono "339.277344" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:47
-xref: uniprot.ptm:PTM-0242
-is_a: MOD:00652
-is_a: MOD:02004
-
-[Term]
-id: MOD:00089
-name: O-palmitoyl-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O-palmitoyl-L-serine." [OMSSA:94, PubMed:3467339, RESID:AA0080, Unimod:47#S]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-(hexadecanoyloxy)propanoic acid" EXACT RESID-systematic []
-synonym: "ACT_SITE O-palmitoyl serine intermediate" EXACT UniProt-feature []
-synonym: "L-serine hexadecanoate ester" EXACT RESID-alternate []
-synonym: "LIPID O-palmitoyl serine" EXACT UniProt-feature []
-synonym: "O-palmitoyl-L-serine" EXACT RESID-name []
-synonym: "O-palmitoylated L-serine" EXACT PSI-MOD-alternate []
-synonym: "O-hexadecanoylated L-serine" EXACT PSI-MOD-alternate []
-synonym: "O3-palmitoyl-serine" EXACT RESID-alternate []
-synonym: "OPamSer" EXACT PSI-MOD-label []
-synonym: "Palmitoyl" RELATED PSI-MS-label []
-synonym: "Palmitoylation" RELATED Unimod-description []
-synonym: "palmitoylations" EXACT OMSSA-label []
-synonym: "serine palmitate ester" EXACT RESID-alternate []
-property_value: DiffAvg "238.41" xsd:float
-property_value: DiffFormula "C 16 H 30 N 0 O 1" xsd:string
-property_value: DiffMono "238.229666" xsd:float
-property_value: Formula "C 19 H 35 N 1 O 3" xsd:string
-property_value: MassAvg "325.49" xsd:float
-property_value: MassMono "325.261694" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:47
-xref: uniprot.ptm:PTM-0241
-is_a: MOD:00652
-is_a: MOD:02003
-
-[Term]
-id: MOD:00090
-name: L-alanine amide
-def: "A protein modification that effectively converts an L-alanine residue to L-alanine amide." [PubMed:1377792, PubMed:2069951, PubMed:8472537, PubMed:952951, RESID:AA0081]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-aminopropanamide" EXACT RESID-systematic []
-synonym: "AlaN" EXACT PSI-MOD-label []
-synonym: "alaninamide" EXACT RESID-alternate []
-synonym: "amidated L-alanine" EXACT PSI-MOD-alternate []
-synonym: "L-alanine amide" EXACT RESID-name []
-synonym: "MOD_RES Alanine amide" EXACT UniProt-feature []
-property_value: DiffAvg "-0.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 1 O -1" xsd:string
-property_value: DiffMono "-0.984016" xsd:float
-property_value: Formula "C 3 H 7 N 2 O 1" xsd:string
-property_value: MassAvg "87.10" xsd:float
-property_value: MassMono "87.055838" xsd:float
-property_value: Origin "A" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0057
-is_a: MOD:00883
-is_a: MOD:00901
-
-[Term]
-id: MOD:00091
-name: L-arginine amide
-def: "A protein modification that effectively converts an L-arginine residue to L-arginine amide." [PubMed:2229025, PubMed:2753890, PubMed:743209, RESID:AA0082, ChEBI:145897]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-5-[(diaminomethylidene)amino]pentanamide" EXACT RESID-systematic []
-synonym: "2-amino-5-carbamimidamidopentanamide" EXACT RESID-alternate []
-synonym: "2-amino-5-guanidinopentanamide" EXACT RESID-alternate []
-synonym: "amidated L-arginine" EXACT PSI-MOD-alternate []
-synonym: "argininamide" EXACT RESID-alternate []
-synonym: "ArgN" EXACT PSI-MOD-label []
-synonym: "L-arginine amide" EXACT RESID-name []
-synonym: "MOD_RES Arginine amide" EXACT UniProt-feature []
-property_value: DiffAvg "-0.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 1 O -1" xsd:string
-property_value: DiffMono "-0.984016" xsd:float
-property_value: Formula "C 6 H 14 N 5 O 1" xsd:string
-property_value: MassAvg "172.21" xsd:float
-property_value: MassMono "172.119835" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0060
-is_a: MOD:00883
-is_a: MOD:00902
-
-[Term]
-id: MOD:00092
-name: L-asparagine amide
-def: "A protein modification that effectively converts an L-asparagine residue to L-asparagine amide." [PubMed:2753132, PubMed:279902, PubMed:3415690, RESID:AA0083, ChEBI:145898]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-aminobutanediamide" EXACT RESID-systematic []
-synonym: "amidated L-asparagine" EXACT PSI-MOD-alternate []
-synonym: "AsnN" EXACT PSI-MOD-label []
-synonym: "asparaginamide" EXACT RESID-alternate []
-synonym: "L-asparagine amide" EXACT RESID-name []
-synonym: "MOD_RES Asparagine amide" EXACT UniProt-feature []
-property_value: DiffAvg "-0.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 1 O -1" xsd:string
-property_value: DiffMono "-0.984016" xsd:float
-property_value: Formula "C 4 H 8 N 3 O 2" xsd:string
-property_value: MassAvg "130.13" xsd:float
-property_value: MassMono "130.061652" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0062
-is_a: MOD:00883
-is_a: MOD:00903
-
-[Term]
-id: MOD:00093
-name: L-aspartic acid 1-amide
-def: "A protein modification that effectively converts an L-aspartic acid residue to L-aspartic acid 1-amide." [PubMed:2542051, RESID:AA0084]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-1-butanediamic acid" EXACT RESID-systematic []
-synonym: "1-amidated L-aspartic acid" EXACT PSI-MOD-alternate []
-synonym: "3,4-diamino-4-oxobutanoic acid" EXACT RESID-alternate []
-synonym: "3-amino-succinamic acid" EXACT RESID-alternate []
-synonym: "alpha-asparagine" EXACT RESID-alternate []
-synonym: "AspN" EXACT PSI-MOD-label []
-synonym: "isoasparagine" EXACT RESID-alternate []
-synonym: "L-aspartic acid 1-amide" EXACT RESID-name []
-synonym: "MOD_RES Aspartic acid 1-amide" EXACT UniProt-feature []
-property_value: DiffAvg "-0.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 1 O -1" xsd:string
-property_value: DiffMono "-0.984016" xsd:float
-property_value: Formula "C 4 H 7 N 2 O 3" xsd:string
-property_value: MassAvg "131.11" xsd:float
-property_value: MassMono "131.045667" xsd:float
-property_value: Origin "D" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0063
-is_a: MOD:00883
-is_a: MOD:00904
-
-[Term]
-id: MOD:00094
-name: L-cysteine amide
-def: "A protein modification that effectively converts an L-cysteine residue to L-cysteine amide." [PubMed:1892838, PubMed:7149738, RESID:AA0085]
-subset: PSI-MOD-slim
-synonym: "(2R)-2-amino-3-sulfanylpropanamide" EXACT RESID-systematic []
-synonym: "2-amino-3-mercaptopropanamide" EXACT RESID-alternate []
-synonym: "amidated L-cysteine" EXACT PSI-MOD-alternate []
-synonym: "CysN" EXACT PSI-MOD-label []
-synonym: "cysteinamide" EXACT RESID-alternate []
-synonym: "L-cysteine amide" EXACT RESID-name []
-synonym: "MOD_RES Cysteine amide" EXACT UniProt-feature []
-property_value: DiffAvg "-0.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 1 O -1 S 0" xsd:string
-property_value: DiffMono "-0.984016" xsd:float
-property_value: Formula "C 3 H 7 N 2 O 1 S 1" xsd:string
-property_value: MassAvg "119.16" xsd:float
-property_value: MassMono "119.027909" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0102
-is_a: MOD:00883
-is_a: MOD:00905
-
-[Term]
-id: MOD:00095
-name: L-glutamine amide
-def: "A protein modification that effectively converts an L-glutamine residue to L-glutamine amide." [PubMed:7673220, PubMed:9048550, RESID:AA0086]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-aminopentanediamide" EXACT RESID-systematic []
-synonym: "amidated L-glutamine" EXACT PSI-MOD-alternate []
-synonym: "GlnN" EXACT PSI-MOD-label []
-synonym: "glutaminamide" EXACT RESID-alternate []
-synonym: "L-glutamine amide" EXACT RESID-name []
-synonym: "MOD_RES Glutamine amide" EXACT UniProt-feature []
-property_value: DiffAvg "-0.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 1 O -1" xsd:string
-property_value: DiffMono "-0.984016" xsd:float
-property_value: Formula "C 5 H 10 N 3 O 2" xsd:string
-property_value: MassAvg "144.15" xsd:float
-property_value: MassMono "144.077302" xsd:float
-property_value: Origin "Q" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0130
-is_a: MOD:00883
-is_a: MOD:00907
-
-[Term]
-id: MOD:00096
-name: L-glutamic acid 1-amide
-def: "A protein modification that effectively converts an L-glutamic acid residue to L-glutamic acid 1-amide." [PubMed:1093875, PubMed:14550575, RESID:AA0087]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-1-pentanediamic acid" EXACT RESID-systematic []
-synonym: "1-amidated L-glutamic acid" EXACT PSI-MOD-alternate []
-synonym: "4,5-diamino-5-oxopentanoic acid" EXACT RESID-alternate []
-synonym: "GluN" EXACT PSI-MOD-label []
-synonym: "isoglutamine" EXACT RESID-alternate []
-synonym: "L-glutamic acid 1-amide" EXACT RESID-name []
-synonym: "MOD_RES Glutamic acid 1-amide" EXACT UniProt-feature []
-property_value: DiffAvg "-0.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 1 O -1" xsd:string
-property_value: DiffMono "-0.984016" xsd:float
-property_value: Formula "C 5 H 9 N 2 O 3" xsd:string
-property_value: MassAvg "145.14" xsd:float
-property_value: MassMono "145.061317" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0129
-is_a: MOD:00883
-is_a: MOD:00906
-
-[Term]
-id: MOD:00097
-name: glycine amide
-def: "A protein modification that effectively converts a glycine residue to glycine amide." [PubMed:13591312, RESID:AA0088]
-subset: PSI-MOD-slim
-synonym: "2-aminoacetamide" EXACT RESID-alternate []
-synonym: "2-aminoethanamide" EXACT RESID-systematic []
-synonym: "2-azanylethanamide" EXACT RESID-alternate []
-synonym: "amidated glycine" EXACT PSI-MOD-alternate []
-synonym: "glycinamide" EXACT RESID-alternate []
-synonym: "glycine amide" EXACT RESID-name []
-synonym: "GlyN" EXACT PSI-MOD-label []
-synonym: "MOD_RES Glycine amide" EXACT UniProt-feature []
-property_value: DiffAvg "-0.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 1 O -1" xsd:string
-property_value: DiffMono "-0.984016" xsd:float
-property_value: Formula "C 2 H 5 N 2 O 1" xsd:string
-property_value: MassAvg "73.07" xsd:float
-property_value: MassMono "73.040188" xsd:float
-property_value: Origin "G" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0132
-is_a: MOD:00883
-is_a: MOD:00908
-
-[Term]
-id: MOD:00098
-name: L-histidine amide
-def: "A protein modification that effectively converts an L-histidine residue to L-histidine amide." [PubMed:2153586, PubMed:2307683, PubMed:2839478, RESID:AA0089]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-(1H-imidazol-4-yl)propanamide" EXACT RESID-systematic []
-synonym: "amidated L-histidine" EXACT PSI-MOD-alternate []
-synonym: "HisN" EXACT PSI-MOD-label []
-synonym: "histidinamide" EXACT RESID-alternate []
-synonym: "L-histidine amide" EXACT RESID-name []
-synonym: "MOD_RES Histidine amide" EXACT UniProt-feature []
-property_value: DiffAvg "-0.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 1 O -1" xsd:string
-property_value: DiffMono "-0.984016" xsd:float
-property_value: Formula "C 6 H 9 N 4 O 1" xsd:string
-property_value: MassAvg "153.16" xsd:float
-property_value: MassMono "153.077636" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0148
-is_a: MOD:00883
-is_a: MOD:00909
-
-[Term]
-id: MOD:00099
-name: L-isoleucine amide
-def: "A protein modification that effectively converts an L-isoleucine residue to L-isoleucine amide." [RESID:AA0090]
-subset: PSI-MOD-slim
-synonym: "(2S,3S)-2-amino-3-methylpentanamide" EXACT RESID-systematic []
-synonym: "amidated L-isoleucine" EXACT PSI-MOD-alternate []
-synonym: "IleN" EXACT PSI-MOD-label []
-synonym: "isoleucinamide" EXACT RESID-alternate []
-synonym: "L-isoleucine amide" EXACT RESID-name []
-synonym: "MOD_RES Isoleucine amide" EXACT UniProt-feature []
-property_value: DiffAvg "-0.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 1 O -1" xsd:string
-property_value: DiffMono "-0.984016" xsd:float
-property_value: Formula "C 6 H 13 N 2 O 1" xsd:string
-property_value: MassAvg "129.18" xsd:float
-property_value: MassMono "129.102788" xsd:float
-property_value: Origin "I" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0161
-is_a: MOD:00883
-is_a: MOD:00910
-
-[Term]
-id: MOD:00100
-name: L-leucine amide
-def: "A protein modification that effectively converts an L-leucine residue to L-leucine amide." [PubMed:2578459, RESID:AA0091]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-4-methylpentanamide" EXACT RESID-systematic []
-synonym: "2-amino-4-methylvaleramide" EXACT RESID-alternate []
-synonym: "2-azanyl-4-methylpentanamide" EXACT RESID-alternate []
-synonym: "alpha-aminoisocaproamide" EXACT RESID-alternate []
-synonym: "amidated L-leucine" EXACT PSI-MOD-alternate []
-synonym: "L-leucine amide" EXACT RESID-name []
-synonym: "leucinamide" EXACT RESID-alternate []
-synonym: "LeuN" EXACT PSI-MOD-label []
-synonym: "MOD_RES Leucine amide" EXACT UniProt-feature []
-property_value: DiffAvg "-0.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 1 O -1" xsd:string
-property_value: DiffMono "-0.984016" xsd:float
-property_value: Formula "C 6 H 13 N 2 O 1" xsd:string
-property_value: MassAvg "129.18" xsd:float
-property_value: MassMono "129.102788" xsd:float
-property_value: Origin "L" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0166
-is_a: MOD:00883
-is_a: MOD:00911
-
-[Term]
-id: MOD:00101
-name: L-lysine amide
-def: "A protein modification that effectively converts an L-lysine residue to L-lysine amide." [PubMed:6579533, RESID:AA0092]
-subset: PSI-MOD-slim
-synonym: "(2S)-2,6-diaminohexanamide" EXACT RESID-systematic []
-synonym: "amidated L-lysine" EXACT PSI-MOD-alternate []
-synonym: "L-lysine amide" EXACT RESID-name []
-synonym: "lysinamide" EXACT RESID-alternate []
-synonym: "LysN" EXACT PSI-MOD-label []
-synonym: "MOD_RES Lysine amide" EXACT UniProt-feature []
-property_value: DiffAvg "-0.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 1 O -1" xsd:string
-property_value: DiffMono "-0.984016" xsd:float
-property_value: Formula "C 6 H 14 N 3 O 1" xsd:string
-property_value: MassAvg "144.20" xsd:float
-property_value: MassMono "144.113687" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0168
-is_a: MOD:00883
-is_a: MOD:00912
-
-[Term]
-id: MOD:00102
-name: L-methionine amide
-def: "A protein modification that effectively converts an L-methionine residue to L-methionine amide." [PubMed:4375977, RESID:AA0093]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-4-(methylsulfanyl)butanamide" EXACT RESID-systematic []
-synonym: "2-amino-4-(methylthio)butanamide" EXACT RESID-alternate []
-synonym: "amidated L-methionine" EXACT PSI-MOD-alternate []
-synonym: "L-methionine amide" EXACT RESID-name []
-synonym: "methioninamide" EXACT RESID-alternate []
-synonym: "MetN" EXACT PSI-MOD-label []
-synonym: "MOD_RES Methionine amide" EXACT UniProt-feature []
-property_value: DiffAvg "-0.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 1 O -1 S 0" xsd:string
-property_value: DiffMono "-0.984016" xsd:float
-property_value: Formula "C 5 H 11 N 2 O 1 S 1" xsd:string
-property_value: MassAvg "147.22" xsd:float
-property_value: MassMono "147.059209" xsd:float
-property_value: Origin "M" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0164
-is_a: MOD:00883
-is_a: MOD:00913
-
-[Term]
-id: MOD:00103
-name: L-phenylalanine amide
-def: "A protein modification that effectively converts an L-phenylalanine residue to L-phenylalanine amide." [PubMed:2905621, PubMed:8868490, RESID:AA0094]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-phenylpropanamide" EXACT RESID-systematic []
-synonym: "amidated L-phenylalanine" EXACT PSI-MOD-alternate []
-synonym: "L-phenylalanine amide" EXACT RESID-name []
-synonym: "MOD_RES Phenylalanine amide" EXACT UniProt-feature []
-synonym: "PheN" EXACT PSI-MOD-label []
-synonym: "phenylalaninamide" EXACT RESID-alternate []
-property_value: DiffAvg "-0.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 1 O -1" xsd:string
-property_value: DiffMono "-0.984016" xsd:float
-property_value: Formula "C 9 H 11 N 2 O 1" xsd:string
-property_value: MassAvg "163.20" xsd:float
-property_value: MassMono "163.087138" xsd:float
-property_value: Origin "F" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0248
-is_a: MOD:00883
-is_a: MOD:00914
-
-[Term]
-id: MOD:00104
-name: L-proline amide
-def: "A protein modification that effectively converts an L-proline residue to L-proline amide." [PubMed:4982117, PubMed:5760861, RESID:AA0095]
-subset: PSI-MOD-slim
-synonym: "(2S)-pyrrolidine-2-carboxamide" EXACT RESID-systematic []
-synonym: "amidated L-proline" EXACT PSI-MOD-alternate []
-synonym: "L-proline amide" EXACT RESID-name []
-synonym: "MOD_RES Proline amide" EXACT UniProt-feature []
-synonym: "prolinamide" EXACT RESID-alternate []
-synonym: "ProN" EXACT PSI-MOD-label []
-property_value: DiffAvg "-0.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 1 O -1" xsd:string
-property_value: DiffMono "-0.984016" xsd:float
-property_value: Formula "C 5 H 9 N 2 O 1" xsd:string
-property_value: MassAvg "113.14" xsd:float
-property_value: MassMono "113.071488" xsd:float
-property_value: Origin "P" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0257
-is_a: MOD:00883
-is_a: MOD:00915
-
-[Term]
-id: MOD:00105
-name: L-serine amide
-def: "A protein modification that effectively converts an L-serine residue to L-serine amide." [PubMed:743209, RESID:AA0096]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-hydroxypropanamide" EXACT RESID-systematic []
-synonym: "amidated L-serine" EXACT PSI-MOD-alternate []
-synonym: "L-serine amide" EXACT RESID-name []
-synonym: "MOD_RES Serine amide" EXACT UniProt-feature []
-synonym: "serinamide" EXACT RESID-alternate []
-synonym: "SerN" EXACT PSI-MOD-label []
-property_value: DiffAvg "-0.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 1 O -1" xsd:string
-property_value: DiffMono "-0.984016" xsd:float
-property_value: Formula "C 3 H 7 N 2 O 2" xsd:string
-property_value: MassAvg "103.10" xsd:float
-property_value: MassMono "103.050752" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0275
-is_a: MOD:00883
-is_a: MOD:00916
-
-[Term]
-id: MOD:00106
-name: L-threonine amide
-def: "A protein modification that effectively converts an L-threonine residue to L-threonine amide." [PubMed:1390774, RESID:AA0097]
-subset: PSI-MOD-slim
-synonym: "(2S,3R)-2-amino-3-hydroxybutanamide" EXACT RESID-systematic []
-synonym: "amidated L-threonine" EXACT PSI-MOD-alternate []
-synonym: "L-threonine amide" EXACT RESID-name []
-synonym: "MOD_RES Threonine amide" EXACT UniProt-feature []
-synonym: "threoninamide" EXACT RESID-alternate []
-synonym: "ThrN" EXACT PSI-MOD-label []
-property_value: DiffAvg "-0.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 1 O -1" xsd:string
-property_value: DiffMono "-0.984016" xsd:float
-property_value: Formula "C 4 H 9 N 2 O 2" xsd:string
-property_value: MassAvg "117.13" xsd:float
-property_value: MassMono "117.066403" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0293
-is_a: MOD:00883
-is_a: MOD:00917
-
-[Term]
-id: MOD:00107
-name: L-tryptophan amide
-def: "A protein modification that effectively converts an L-tryptophan residue to L-tryptophan amide." [PubMed:3947348, RESID:AA0098]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-(1H-indol-3-yl)propanamide" EXACT RESID-systematic []
-synonym: "amidated L-tryptophan" EXACT PSI-MOD-alternate []
-synonym: "L-tryptophan amide" EXACT RESID-name []
-synonym: "MOD_RES Tryptophan amide" EXACT UniProt-feature []
-synonym: "TrpN" EXACT PSI-MOD-label []
-synonym: "tryptophanamide" EXACT RESID-alternate []
-property_value: DiffAvg "-0.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 1 O -1" xsd:string
-property_value: DiffMono "-0.984016" xsd:float
-property_value: Formula "C 11 H 12 N 3 O 1" xsd:string
-property_value: MassAvg "202.24" xsd:float
-property_value: MassMono "202.098037" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0296
-is_a: MOD:00883
-is_a: MOD:00918
-
-[Term]
-id: MOD:00108
-name: L-tyrosine amide
-def: "A protein modification that effectively converts an L-tyrosine residue to L-tyrosine amide." [PubMed:1377792, PubMed:3562898, PubMed:6509012, RESID:AA0099]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-(4-hydoxyphenyl)propanamide" EXACT RESID-systematic []
-synonym: "amidated L-tyrosine" EXACT PSI-MOD-alternate []
-synonym: "L-tyrosine amide" EXACT RESID-name []
-synonym: "MOD_RES Tyrosine amide" EXACT UniProt-feature []
-synonym: "TyrN" EXACT PSI-MOD-label []
-synonym: "tyrosinamide" EXACT RESID-alternate []
-property_value: DiffAvg "-0.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 1 O -1" xsd:string
-property_value: DiffMono "-0.984016" xsd:float
-property_value: Formula "C 9 H 11 N 2 O 2" xsd:string
-property_value: MassAvg "179.20" xsd:float
-property_value: MassMono "179.082053" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0302
-is_a: MOD:00883
-is_a: MOD:00919
-
-[Term]
-id: MOD:00109
-name: L-valine amide
-def: "A protein modification that effectively converts an L-valine residue to L-valine amide." [PubMed:2578459, PubMed:5465996, RESID:AA0100]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-methylbutanamide" EXACT RESID-systematic []
-synonym: "L-valine amide" EXACT RESID-name []
-synonym: "MOD_RES Valine amide" EXACT UniProt-feature []
-synonym: "valinamide" EXACT RESID-alternate []
-synonym: "ValN" EXACT PSI-MOD-label []
-property_value: DiffAvg "-0.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 1 O -1" xsd:string
-property_value: DiffMono "-0.984016" xsd:float
-property_value: Formula "C 5 H 11 N 2 O 1" xsd:string
-property_value: MassAvg "115.16" xsd:float
-property_value: MassMono "115.087138" xsd:float
-property_value: Origin "V" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0303
-is_a: MOD:00883
-is_a: MOD:00920
-
-[Term]
-id: MOD:00110
-name: L-cysteine methyl disulfide
-def: "A protein modification that effectively converts an L-cysteine residue to L-cysteine methyl disulfide." [OMSSA:179, PubMed:10555576, PubMed:163643, PubMed:2056535, PubMed:6381494, RESID:AA0101, Unimod:39#C]
-comment: Produced artifactually by reaction of cysteine residues with methyl methanethiosulfonate (MMTS) [JSG], but also naturally in bacteria [PMT].
-synonym: "(2R)-2-amino-3-(methyldisulfanediyl)propanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-3-(methyldisulfanediyl)propanoic acid" EXACT RESID-alternate []
-synonym: "2-amino-3-(methyldithio)propanoic acid" EXACT RESID-alternate []
-synonym: "2-amino-3-methyldisulfanylpropanoic acid" EXACT RESID-alternate []
-synonym: "2-azanyl-3-(methyldisulfanediyl)-propanoic acid" EXACT RESID-alternate []
-synonym: "Beta-methylthiolation" RELATED Unimod-description []
-synonym: "L-3-(methyldithio)alanine" EXACT RESID-alternate []
-synonym: "L-cysteine methyl disulfide" EXACT RESID-name []
-synonym: "methyl methanethiolsulfonate derivatized cysteine" EXACT PSI-MOD-alternate []
-synonym: "methyl methanethiosulfonate derivatized cysteine" EXACT PSI-MOD-alternate []
-synonym: "Methylthio" RELATED PSI-MS-label []
-synonym: "Methylthio" RELATED Unimod-interim []
-synonym: "mmts" EXACT OMSSA-label []
-synonym: "MOD_RES Cysteine methyl disulfide" EXACT UniProt-feature []
-synonym: "S-methylthio-L-cysteine" EXACT RESID-alternate []
-synonym: "S-methylthiocysteine" EXACT RESID-alternate []
-property_value: DiffAvg "46.09" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0 S 1" xsd:string
-property_value: DiffMono "45.987721" xsd:float
-property_value: Formula "C 4 H 7 N 1 O 1 S 2" xsd:string
-property_value: MassAvg "149.23" xsd:float
-property_value: MassMono "148.996906" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:39
-xref: uniprot.ptm:PTM-0104
-is_a: MOD:00848
-is_a: MOD:00905
-is_a: MOD:01153
-is_a: MOD:01862
-
-[Term]
-id: MOD:00111
-name: S-farnesyl-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-farnesyl-L-cysteine." [DeltaMass:293, OMSSA:42, PubMed:1409665, PubMed:15609361, PubMed:1872463, PubMed:2684976, RESID:AA0102, Unimod:44#C]
-comment: From DeltaMass: (name misspelled \"S-farnesyl cystenyl\")
-subset: PSI-MOD-slim
-synonym: "(2R)-2-amino-3-([(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]sulfanyl)propanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-3-(3,7,11-trimethyl-2,6,10-dodecatrienylthio)propanoic acid" EXACT RESID-alternate []
-synonym: "Farnesyl" RELATED PSI-MS-label []
-synonym: "Farnesylation" RELATED Unimod-description []
-synonym: "farnesylationc" EXACT OMSSA-label []
-synonym: "LIPID S-farnesyl cysteine" EXACT UniProt-feature []
-synonym: "S-farnesyl Cystenyl" EXACT DeltaMass-label []
-synonym: "S-farnesyl-L-cysteine" EXACT RESID-name []
-synonym: "SFarnCys" EXACT PSI-MOD-label []
-property_value: DiffAvg "204.36" xsd:float
-property_value: DiffFormula "C 15 H 24 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "204.187801" xsd:float
-property_value: Formula "C 18 H 29 N 1 O 1 S 1" xsd:string
-property_value: MassAvg "307.50" xsd:float
-property_value: MassMono "307.196986" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:44
-xref: uniprot.ptm:PTM-0277
-is_a: MOD:00437
-is_a: MOD:01110
-
-[Term]
-id: MOD:00112
-name: S-12-hydroxyfarnesyl-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-12-hydroxyfarnesyl-L-cysteine." [PubMed:17790543, RESID:AA0103, Unimod:376]
-synonym: "(2R)-2-amino-3-([(2E,6E,10Z)-12-hydroxy-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]sulfanyl)propanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-3-(12-hydroxy-3,7,11-trimethyl-3,6,10-dodecatrienylthio)propanoic acid" EXACT RESID-alternate []
-synonym: "Hydroxyfarnesyl" RELATED PSI-MS-label []
-synonym: "hydroxyfarnesyl" RELATED Unimod-description []
-synonym: "LIPID S-12-hydroxyfarnesyl cysteine" EXACT UniProt-feature []
-synonym: "S-12-hydroxyfarnesyl-L-cysteine" EXACT RESID-name []
-synonym: "S12HyFarnCys" EXACT PSI-MOD-label []
-property_value: DiffAvg "220.36" xsd:float
-property_value: DiffFormula "C 15 H 24 N 0 O 1 S 0" xsd:string
-property_value: DiffMono "220.182715" xsd:float
-property_value: Formula "C 18 H 29 N 1 O 2 S 1" xsd:string
-property_value: MassAvg "323.50" xsd:float
-property_value: MassMono "323.191900" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:376
-xref: uniprot.ptm:PTM-0269
-is_a: MOD:01110
-
-[Term]
-id: MOD:00113
-name: S-geranylgeranyl-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-geranylgeranyl-L-cysteine." [DeltaMass:0, OMSSA:49, PubMed:1483450, PubMed:15609361, RESID:AA0104, Unimod:48#C]
-comment: DeltaMass calculates the mass with two double bonds rather than four
-subset: PSI-MOD-slim
-synonym: "(2R)-2-amino-3-([(2E,6E,10Z)-12-hydroxy-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]sulfanyl)propanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-3-(3,7,11,15-tetramethyl-2,6,10,14-hexadecatetraenylthio)propanoic acid" EXACT RESID-alternate []
-synonym: "Geranyl-geranyl" RELATED Unimod-description []
-synonym: "GeranylGeranyl" RELATED PSI-MS-label []
-synonym: "geranylgeranylc" EXACT OMSSA-label []
-synonym: "LIPID S-geranylgeranyl cysteine" EXACT UniProt-feature []
-synonym: "S-geranylgeranyl" EXACT DeltaMass-label []
-synonym: "S-geranylgeranyl-L-cysteine" EXACT RESID-name []
-synonym: "SGergerCys" EXACT PSI-MOD-label []
-property_value: DiffAvg "272.48" xsd:float
-property_value: DiffFormula "C 20 H 32 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "272.250401" xsd:float
-property_value: Formula "C 23 H 37 N 1 O 1 S 1" xsd:string
-property_value: MassAvg "375.62" xsd:float
-property_value: MassMono "375.259586" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:48
-xref: uniprot.ptm:PTM-0278
-is_a: MOD:00441
-is_a: MOD:01110
-
-[Term]
-id: MOD:00114
-name: L-cysteine methyl ester
-def: "A protein modification that effectively converts an L-cysteine residue to L-cysteine methyl ester." [PubMed:11875433, PubMed:1872463, RESID:AA0105, Unimod:34#C-term]
-comment: Secondary to RESID:AA0102; secondary to RESID:AA0103; secondary to RESID:AA0104.
-subset: PSI-MOD-slim
-synonym: "2-amino-3-mercaptopropanoic methyl ester" EXACT RESID-alternate []
-synonym: "2-amino-3-sulfanylpropanoic methyl ester" EXACT RESID-alternate []
-synonym: "L-cysteine methyl ester" EXACT RESID-name []
-synonym: "mecysteine" EXACT RESID-alternate []
-synonym: "Methyl" RELATED PSI-MS-label []
-synonym: "methyl (2R)-2-amino-3-sulfanylpropanoate" EXACT RESID-systematic []
-synonym: "methyl esterified L-cysteine" EXACT PSI-MOD-alternate []
-synonym: "methyl L-cysteinate" EXACT RESID-alternate []
-synonym: "Methylation" RELATED Unimod-description []
-synonym: "MOD_RES Cysteine methyl ester" EXACT UniProt-feature []
-synonym: "OMeCys" EXACT PSI-MOD-label []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 4 H 8 N 1 O 2 S 1" xsd:string
-property_value: MassAvg "134.17" xsd:float
-property_value: MassMono "134.027574" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: Unimod:34
-xref: uniprot.ptm:PTM-0105
-is_a: MOD:01682
-is_a: MOD:01689
-
-[Term]
-id: MOD:00115
-name: S-palmitoyl-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-palmitoyl-L-cysteine." [DeltaMass:303, PubMed:1872406, PubMed:3166978, PubMed:8180229, PubMed:8824274, RESID:AA0106, Unimod:47#C]
-comment: From DeltaMass: (name misspelled \"S-palmityl Cystenyl\" and formula incorrect, N and O reversed) Formula: C19H35O1N2S1 Monoisotopic Mass Change: 341.239 Average Mass Change: 341.556
-subset: PSI-MOD-slim
-synonym: "(2R)-2-amino-3-(hexadecanoylsulfanyl)propanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-3-(hexadecanoylthio)propanoic acid" EXACT RESID-alternate []
-synonym: "ACT_SITE S-palmitoyl cysteine intermediate" EXACT UniProt-feature []
-synonym: "cysteine hexadecanoate thioester" EXACT RESID-alternate []
-synonym: "cysteine palmitate thioester" EXACT RESID-alternate []
-synonym: "LIPID S-palmitoyl cysteine" EXACT UniProt-feature []
-synonym: "Palmitoyl" RELATED PSI-MS-label []
-synonym: "Palmitoylation" RELATED Unimod-description []
-synonym: "S-palmitoyl-L-cysteine" EXACT RESID-name []
-synonym: "S-palmitoylated L-cysteine" EXACT PSI-MOD-alternate []
-synonym: "S-hexadecanoylated L-cysteine" EXACT PSI-MOD-alternate []
-synonym: "S-palmityl Cystenyl" EXACT DeltaMass-label []
-synonym: "SPamCys" EXACT PSI-MOD-label []
-property_value: DiffAvg "238.41" xsd:float
-property_value: DiffFormula "C 16 H 30 N 0 O 1 S 0" xsd:string
-property_value: DiffMono "238.229666" xsd:float
-property_value: Formula "C 19 H 35 N 1 O 2 S 1" xsd:string
-property_value: MassAvg "341.55" xsd:float
-property_value: MassMono "341.238850" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:47
-xref: uniprot.ptm:PTM-0281
-is_a: MOD:00653
-is_a: MOD:01684
-
-[Term]
-id: MOD:00116
-name: S-diacylglycerol-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-diacylglycerol-L-cysteine." [PubMed:10896212, PubMed:4575979, PubMed:9056182, RESID:AA0107, Unimod:377#C]
-comment: Incidental to RESID:AA0060.
-subset: PSI-MOD-slim
-synonym: "(2R)-2-amino-3-[(2S)-2-((9Z)-9-octadecenoyloxy)-3-(hexadecanoyloxy)propyl]sulfanylpropanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-3-[(S)-2-((Z)-9-octadecenoyloxy)-3-(hexadecanoyloxy)propyl]thiopropanoic acid" EXACT RESID-alternate []
-synonym: "Diacylglycerol" RELATED PSI-MS-label []
-synonym: "diacylglycerol" RELATED Unimod-description []
-synonym: "LIPID S-diacylglycerol cysteine" EXACT UniProt-feature []
-synonym: "S-(1-2'-oleoyl-3'-palmitoyl-glycerol)cysteine" EXACT RESID-alternate []
-synonym: "S-(2',3'-diacylglycerol)-L-cysteine" EXACT PSI-MOD-alternate []
-synonym: "S-diacylglycerol-L-cysteine" EXACT RESID-name []
-synonym: "SAcyl2GlyceroCys" EXACT PSI-MOD-label []
-xref: uniprot.ptm:PTM-0274
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00905
-is_a: MOD:01155
-
-[Term]
-id: MOD:00117
-name: S-(L-isoglutamyl)-L-cysteine
-def: "A protein modification that effectively crosslinks an L-cysteine residue and an L-glutamine residue by a thioester bond with the formation of S-(L-isoglutamyl)-L-cysteine and the release of ammonia." [ChEBI:22021, DeltaMass:0, PubMed:6838833, RESID:AA0108]
-comment: Cross-link 2; DeltaMass calculates the mass difference from glutamic acid rather than glutamine.
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-5-[(2R)-2-amino-2-carboxyethyl]sulfanyl-5-oxopentanoic acid" EXACT RESID-systematic []
-synonym: "(S,R)-2-amino-4-[S-(2-amino-2-carboxyethyl)thiocarboxy]butanoic acid" EXACT RESID-alternate []
-synonym: "2-amino-5-(2-amino-2-carboxyethyl)thio-5-oxopentanoic acid" EXACT RESID-alternate []
-synonym: "CROSSLNK Isoglutamyl cysteine thioester (Cys-Gln)" EXACT UniProt-feature []
-synonym: "gamma-(S-cysteinyl)glutamic acid" EXACT RESID-alternate []
-synonym: "S-(L-isoglutamyl)-L-cysteine" EXACT RESID-name []
-synonym: "S-gamma-glutamyl (crosslinked to cysteine)" EXACT DeltaMass-label []
-synonym: "XLNK-SCys-5Glu(Gln)" EXACT PSI-MOD-label []
-property_value: DiffAvg "-17.03" xsd:float
-property_value: DiffFormula "C 0 H -3 N -1 O 0 S 0" xsd:string
-property_value: DiffMono "-17.026549" xsd:float
-property_value: Formula "C 8 H 10 N 2 O 3 S 1" xsd:string
-property_value: MassAvg "214.24" xsd:float
-property_value: MassMono "214.041213" xsd:float
-property_value: Origin "C, Q" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0156
-is_a: MOD:00395
-is_a: MOD:02046
-is_a: MOD:00946
-
-[Term]
-id: MOD:00118
-name: 2'-(S-L-cysteinyl)-L-histidine
-def: "A protein modification that effectively cross-links an L-cysteine residue and an L-histidine residue by a thioether bond to form 2'-(S-L-cysteinyl)-L-histidine." [DeltaMass:0, PubMed:6210696, RESID:AA0109]
-comment: Cross-link 2.
-synonym: "(2R)-2-amino-3-[(4-[(2S)-2-amino-2-carboxyethyl]-1H-imidazol-2-yl)sulfanyl]propanoic acid" EXACT RESID-systematic []
-synonym: "(2S)-2-amino-3-[2-([(2R)-2-amino-2-carboxyethyl]sulfanyl)-1H-imidazol-4-yl]propanoic acid" EXACT RESID-alternate []
-synonym: "2'-(L-cystein-S-yl)-L-histidine" EXACT RESID-name []
-synonym: "CROSSLNK 2'-(S-cysteinyl)-histidine (Cys-His)" EXACT UniProt-feature []
-synonym: "S-(2'-histidyl)cysteine" EXACT RESID-alternate []
-synonym: "S-(2-histidyl)- (crosslinked to cysteine)" EXACT DeltaMass-label []
-synonym: "XLNK-SCys-2'His" EXACT PSI-MOD-label []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 9 H 10 N 4 O 2 S 1" xsd:string
-property_value: MassAvg "238.26" xsd:float
-property_value: MassMono "238.052447" xsd:float
-property_value: Origin "C, H" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0005
-is_a: MOD:00687
-is_a: MOD:02048
-
-[Term]
-id: MOD:00119
-name: L-lanthionine (Cys-Ser)
-def: "A protein modification that effectively cross-links an L-cysteine residue and an L-serine residue by a thioether bond to form L-lanthionine." [ChEBI:21347, DeltaMass:7, RESID:AA0110#CSX]
-comment: Cross-link 2. The natural occurrence of this modification is rare. For the more common modification see MOD:00120 meso-lanthionine [JSG].
-synonym: "(2R,2'R)-3,3'-sulfanediylbis(2-aminopropanoic acid)" EXACT RESID-systematic []
-synonym: "(R)-S-(2-amino-2-carboxyethyl)-L-cysteine" EXACT RESID-alternate []
-synonym: "(R,R)-2,6-diamino-4-thiaheptanedioic acid" EXACT RESID-alternate []
-synonym: "(R,R)-3,3'-thiobis-(2-aminopropanoic acid)" EXACT RESID-alternate []
-synonym: "(R,R)-bis(2-amino-2-carboxyethyl)sulfide" EXACT RESID-alternate []
-synonym: "2-amino-3-(2-amino-2-carboxyethyl)sulfanylpropanoic acid" EXACT RESID-alternate []
-synonym: "3,3'-thiobis-L-alanine" EXACT RESID-alternate []
-synonym: "L-lanthionine" EXACT RESID-name []
-synonym: "XLNK-SCys-(L)3Dha" EXACT PSI-MOD-label []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 6 H 8 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "172.20" xsd:float
-property_value: MassMono "172.030649" xsd:float
-property_value: Origin "C, S" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02055
-is_a: MOD:00954
-is_a: MOD:01839
-
-[Term]
-id: MOD:00120
-name: meso-lanthionine
-def: "A protein modification that effectively cross-links an L-cysteine residue and an L-serine residue by a thioether bond to form meso-lanthionine." [PubMed:15023056, PubMed:3769923, RESID:AA0111]
-comment: Cross-link 2.
-synonym: "(2R,2'S)-3,3'-sulfanediylbis(2-aminopropanoic acid)" EXACT RESID-systematic []
-synonym: "(2R,2'S)-3,3'-thiobis-(2-aminopropanoic acid)" EXACT RESID-alternate []
-synonym: "(2R,6S)-2,6-diamino-4-thiaheptanedioic acid" EXACT RESID-alternate []
-synonym: "(2R,6S)-meso-lanthionine" EXACT RESID-alternate []
-synonym: "(2S)-2-amino-3-[[(2R)-2-amino-2-carboxyethyl]sulfanyl]propanoic acid" EXACT RESID-alternate []
-synonym: "(2S,6R)-meso-lanthionine" RELATED RESID-misnomer []
-synonym: "(R)-S-(2-amino-2-carboxyethyl)-D-cysteine" EXACT RESID-alternate []
-synonym: "(R,S)-bis(2-amino-2-carboxyethyl)sulfide" EXACT RESID-alternate []
-synonym: "3,3'-thiobis-meso-alanine" EXACT RESID-alternate []
-synonym: "CROSSLNK Lanthionine (Cys-Ser)" EXACT UniProt-feature []
-synonym: "CROSSLNK Lanthionine (Ser-Cys)" EXACT UniProt-feature []
-synonym: "cysteine-3-D-alanine thioether" EXACT RESID-alternate []
-synonym: "meso-lanthionine" EXACT RESID-name []
-synonym: "XLNK-SCys-(D)3Dha" EXACT PSI-MOD-label []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 6 H 8 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "172.20" xsd:float
-property_value: MassMono "172.030649" xsd:float
-property_value: Origin "C, S" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0164
-is_a: MOD:02055
-is_a: MOD:00954
-is_a: MOD:01841
-
-[Term]
-id: MOD:00121
-name: (2S,3S,2'R)-3-methyllanthionine
-def: "A protein modification that effectively cross-links an L-cysteine residue and an L-threonine residue by a thioether bond to form (2S,3S,2'R)-3-methyllanthionine." [PubMed:3769923, RESID:AA0112]
-comment: Cross-link 2.
-synonym: "(2S,3S)-2-amino-3-([(2R)-2-amino-2-carboxyethyl]sulfanyl)butanoic acid" EXACT RESID-systematic []
-synonym: "(2S,3S,2'R)-2-amino-3-[(2-amino-2-carboxyethyl)thio]butanoic acid" EXACT RESID-alternate []
-synonym: "(2S,3S,2'R)-3-methyllanthionine" EXACT RESID-name []
-synonym: "(2S,3S,6R)-2,6-diamino-3-methyl-4-thiaheptanedioic acid" EXACT RESID-alternate []
-synonym: "(2S,3S,6R)-3-methyllanthionine" EXACT RESID-alternate []
-synonym: "(2S-[2R*,3R*(S*)])-2-amino-3-[(2-amino-2-carboxyethyl)thio]butanoic acid" EXACT RESID-alternate []
-synonym: "3-methyl-D,L-lanthionine" EXACT RESID-alternate []
-synonym: "CROSSLNK Beta-methyllanthionine (Cys-Thr)" EXACT UniProt-feature []
-synonym: "CROSSLNK Beta-methyllanthionine (Thr-Cys)" EXACT UniProt-feature []
-synonym: "cysteine-3-D-butyrine thioether" EXACT RESID-alternate []
-synonym: "XLNK-SCys-3Dhb" EXACT PSI-MOD-label []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 7 H 10 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "186.23" xsd:float
-property_value: MassMono "186.046299" xsd:float
-property_value: Origin "C, T" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0067
-is_a: MOD:01981
-
-[Term]
-id: MOD:00122
-name: 3'-(S-L-cysteinyl)-L-tyrosine
-def: "A protein modification that effectively cross-links an L-cysteine residue and an L-tyrosine residue by a thioether bond to form 2-(S-L-cysteinyl)-L-tyrosine." [DeltaMass:0, PubMed:15917234, PubMed:2002850, RESID:AA0113]
-comment: Cross-link 2.
-synonym: "(2S)-2-amino-3-(3-[(2R)2-amino-2-carboxyethylsulfanyl]-4-hydroxyphenyl)propanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-3-[3-(2-amino-2-carboxyethylthio)-4-hydroxyphenyl]propanoic acid" EXACT RESID-alternate []
-synonym: "3'-(cystein-S-yl)tyrosine" EXACT RESID-alternate []
-synonym: "3'-(L-cystein-S-yl)-L-tyrosine" EXACT RESID-name []
-synonym: "CROSSLNK 3'-(S-cysteinyl)-tyrosine (Cys-Tyr)" EXACT UniProt-feature []
-synonym: "CROSSLNK 3'-(S-cysteinyl)-tyrosine (Tyr-Cys)" EXACT UniProt-feature []
-synonym: "S-(3-Tyr) (Crosslinked to Cysteine)" EXACT DeltaMass-label []
-synonym: "S-(tyros-3'-yl)cysteine" EXACT RESID-alternate []
-synonym: "XLNK-SCys-3'Tyr" EXACT PSI-MOD-label []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 12 H 12 N 2 O 3 S 1" xsd:string
-property_value: MassAvg "264.30" xsd:float
-property_value: MassMono "264.056863" xsd:float
-property_value: Origin "C, Y" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0019
-is_a: MOD:00687
-is_a: MOD:02058
-
-[Term]
-id: MOD:00123
-name: N6-carboxy-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-carboxy-L-lysine." [PubMed:11369851, PubMed:4436319, PubMed:637859, PubMed:7754395, RESID:AA0114, Unimod:299#K]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-6-(carboxyamino)hexanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-6-carbamic hexanoic acid" EXACT RESID-alternate []
-synonym: "Carboxy" RELATED Unimod-interim []
-synonym: "Carboxylation" RELATED Unimod-description []
-synonym: "lysine NZ-carboxylic acid" EXACT RESID-alternate []
-synonym: "MOD_RES N6-carboxylysine" EXACT UniProt-feature []
-synonym: "N6-carbamyllysine" RELATED RESID-misnomer []
-synonym: "N6-carboxy-L-lysine" EXACT RESID-name []
-synonym: "N6-carboxylysine" EXACT RESID-alternate []
-synonym: "N6CbxLys" EXACT PSI-MOD-label []
-property_value: DiffAvg "44.01" xsd:float
-property_value: DiffFormula "C 1 H 0 N 0 O 2" xsd:string
-property_value: DiffMono "43.989829" xsd:float
-property_value: Formula "C 7 H 12 N 2 O 3" xsd:string
-property_value: MassAvg "172.18" xsd:float
-property_value: MassMono "172.084792" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:299
-xref: uniprot.ptm:PTM-0191
-is_a: MOD:00912
-is_a: MOD:01152
-
-[Term]
-id: MOD:00124
-name: N6-1-carboxyethyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-1-carboxyethyl-L-lysine." [PubMed:3123486, PubMed:8253186, PubMed:8421682, RESID:AA0115, Unimod:378#K]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-6-([(1S)-1-carboxyethyl]amino)hexanoic acid" EXACT RESID-systematic []
-synonym: "Carboxyethyl" RELATED PSI-MS-label []
-synonym: "carboxyethyl" RELATED Unimod-description []
-synonym: "MOD_RES N6-1-carboxyethyl lysine" EXACT UniProt-feature []
-synonym: "N6-(1-carboxyethyl)-L-lysine" EXACT RESID-name []
-synonym: "N6-(1-carboxyethyl)lysine" EXACT RESID-alternate []
-synonym: "N6CbzEtLys" EXACT PSI-MOD-label []
-synonym: "NZ-(1-carboxyethyl)lysine" EXACT RESID-alternate []
-property_value: DiffAvg "72.06" xsd:float
-property_value: DiffFormula "C 3 H 4 N 0 O 2" xsd:string
-property_value: DiffMono "72.021129" xsd:float
-property_value: Formula "C 9 H 16 N 2 O 3" xsd:string
-property_value: MassAvg "200.24" xsd:float
-property_value: MassMono "200.116092" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:378
-xref: uniprot.ptm:PTM-0189
-is_a: MOD:00912
-
-[Term]
-id: MOD:00125
-name: hypusine
-def: "A protein modification that effectively converts an L-lysine residue to hypusine, N6-(4-amino-2-hydroxybutyl)-L-lysine." [DeltaMass:0, PubMed:6806267, PubMed:8108861, RESID:AA0116, Unimod:379#K]
-comment: This modification occurs uniquely in translation initiation factor eIF-5A [JSG].
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-6-([(2R)-4-amino-2-hydroxybutyl]amino)hexanoic acid" EXACT RESID-systematic []
-synonym: "(2S,9R)-2,11-diazanyl-9-hydroxy-7-azaundecanoic acid" EXACT RESID-alternate []
-synonym: "(2S,9R)-hypusine" EXACT RESID-alternate []
-synonym: "2-azanyl-6-[(4-azanyl-2-hydroxybutyl)azanyl]hexanoic acid" EXACT RESID-alternate []
-synonym: "Hypu" EXACT PSI-MOD-label []
-synonym: "Hypusine" RELATED PSI-MS-label []
-synonym: "hypusine" RELATED Unimod-description []
-synonym: "L-hypusine" EXACT RESID-name []
-synonym: "MOD_RES Hypusine" EXACT UniProt-feature []
-synonym: "N-(4-NH2-2-OH-butyl)- (of Lysine)" EXACT DeltaMass-label []
-synonym: "N6-(4-amino-2-hydroxybutyl)-L-lysine" EXACT RESID-alternate []
-property_value: DiffAvg "87.12" xsd:float
-property_value: DiffFormula "C 4 H 9 N 1 O 1" xsd:string
-property_value: DiffMono "87.068414" xsd:float
-property_value: Formula "C 10 H 21 N 3 O 2" xsd:string
-property_value: MassAvg "215.30" xsd:float
-property_value: MassMono "215.163377" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:379
-xref: uniprot.ptm:PTM-0150
-is_a: MOD:00912
-is_a: MOD:01884
-relationship: derives_from MOD:01880
-
-[Term]
-id: MOD:00126
-name: N6-biotinyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-biotinyl-L-lysine." [DeltaMass:305, PubMed:16109483, PubMed:3178228, PubMed:7948875, PubMed:8747466, RESID:AA0117, Unimod:3#K]
-comment: From DeltaMass: Average Mass: 354 Formula:C 16 H 26 O 4 N 3 S 1 (formula incorrect, N and O reversed) Monoisotopic Mass Change:354.172 Average Mass Change:354.471 References:PE Sciex.
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-6-(5-[(3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl]pentanoylamino)hexanoic acid" EXACT RESID-systematic []
-synonym: "(3aS-(3aalpha,4beta,6aalpha))-N6-(5-(hexahydro-2-oxo-1H-thieno(3,4-d)imidazol-4-yl)-1-oxopentyl)-L-lysine" EXACT RESID-alternate []
-synonym: "biocytin" EXACT RESID-alternate []
-synonym: "Biotin" RELATED PSI-MS-label []
-synonym: "biotinyl lysyl" EXACT DeltaMass-label []
-synonym: "Biotinylation" RELATED Unimod-description []
-synonym: "epsilon-N-biotinyllysine" EXACT RESID-alternate []
-synonym: "MOD_RES N6-biotinyllysine" EXACT UniProt-feature []
-synonym: "N6-[5-((3aS,4S,6aR)-hexahydro-2-oxo-1H-thieno[3,4-d]imidazol-4-yl)-1-oxopentyl]-L-lysine" EXACT RESID-alternate []
-synonym: "N6-biotinyl-L-lysine" EXACT RESID-name []
-synonym: "N6-biotinyllysine" EXACT RESID-alternate []
-synonym: "N6BtnLys" EXACT PSI-MOD-label []
-property_value: DiffAvg "226.29" xsd:float
-property_value: DiffFormula "C 10 H 14 N 2 O 2 S 1" xsd:string
-property_value: DiffMono "226.077599" xsd:float
-property_value: Formula "C 16 H 26 N 4 O 3 S 1" xsd:string
-property_value: MassAvg "354.47" xsd:float
-property_value: MassMono "354.172562" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:3
-xref: uniprot.ptm:PTM-0382
-is_a: MOD:01875
-is_a: MOD:01885
-
-[Term]
-id: MOD:00127
-name: N6-lipoyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-lipoyl-L-lysine." [DeltaMass:0, OMSSA:67, PubMed:3421911, PubMed:3522581, PubMed:7719855, RESID:AA0118, Unimod:42#K]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-6-(5-[(3R)-1,2-dithiolan-3-yl]pentanamido)hexanoic acid" EXACT RESID-alternate []
-synonym: "(2S)-2-amino-6-[(5-[(3R)-1,2-dithiolan-3-yl]pentanoyl)amino]hexanoic acid" EXACT RESID-systematic []
-synonym: "(2S,6'R)-2-amino-6-(6,8-dithiooctanamido)hexanoic acid" EXACT RESID-alternate []
-synonym: "2-amino-6-(5-[1,2-dithiolan-3-yl]-1-oxopentyl)aminohexanoic acid" EXACT RESID-alternate []
-synonym: "Lipoyl" RELATED PSI-MS-label []
-synonym: "Lipoyl" RELATED Unimod-description []
-synonym: "lipoylk" EXACT OMSSA-label []
-synonym: "MOD_RES N6-lipoyllysine" EXACT UniProt-feature []
-synonym: "N-Lipoyl- (on Lysine)" EXACT DeltaMass-label []
-synonym: "N6-6,8-dithiooctanoyllysine" EXACT RESID-alternate []
-synonym: "N6-lipoyl-L-lysine" EXACT RESID-name []
-synonym: "N6-lipoyllysine" EXACT RESID-alternate []
-synonym: "N6LipLys" EXACT PSI-MOD-label []
-property_value: DiffAvg "188.30" xsd:float
-property_value: DiffFormula "C 8 H 12 N 0 O 1 S 2" xsd:string
-property_value: DiffMono "188.032957" xsd:float
-property_value: Formula "C 14 H 24 N 2 O 2 S 2" xsd:string
-property_value: MassAvg "316.48" xsd:float
-property_value: MassMono "316.127920" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:42
-xref: uniprot.ptm:PTM-0383
-is_a: MOD:01875
-
-[Term]
-id: MOD:00128
-name: N6-pyridoxal phosphate-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-pyridoxal phosphate-L-lysine." [DeltaMass:0, PubMed:1544460, RESID:AA0119, Unimod:46#K]
-comment: From DeltaMass: Average Mass: 231
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-6-[([3-hydroxy-2-methyl-5-phosphonooxymethylpyridin-4-yl]methylidene)amino]hexanoic acid" EXACT RESID-systematic []
-synonym: "MOD_RES N6-(pyridoxal phosphate)lysine" EXACT UniProt-feature []
-synonym: "N6-pyridoxal phosphate-L-lysine" EXACT RESID-name []
-synonym: "N6PydoxLys" EXACT PSI-MOD-label []
-synonym: "Pyridoxal phosphate" RELATED Unimod-description []
-synonym: "Pyridoxal phosphate (Schiff Base formed to lysine)" EXACT DeltaMass-label []
-synonym: "PyridoxalPhosphate" RELATED PSI-MS-label []
-property_value: DiffAvg "229.13" xsd:float
-property_value: DiffFormula "C 8 H 8 N 1 O 5 P 1" xsd:string
-property_value: DiffMono "229.014009" xsd:float
-property_value: Formula "C 14 H 20 N 3 O 6 P 1" xsd:string
-property_value: MassAvg "357.30" xsd:float
-property_value: MassMono "357.108972" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:46
-xref: uniprot.ptm:PTM-0387
-is_a: MOD:00912
-
-[Term]
-id: MOD:00129
-name: N6-retinylidene-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-retinylidene-L-lysine, the adduct of retinal." [PubMed:6794028, PubMed:6870827, RESID:AA0120, Unimod:380#K]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-6-[(2E,4E,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-en-1-yl)-2,4,6,8-nonatetraenylidene]aminohexanoic acid" EXACT RESID-systematic []
-synonym: "MOD_RES N6-(retinylidene)lysine" EXACT UniProt-feature []
-synonym: "N6-retinal-L-lysine" EXACT RESID-alternate []
-synonym: "N6-retinyl-lysine" EXACT RESID-alternate []
-synonym: "N6-retinylidene-L-lysine" EXACT RESID-name []
-synonym: "N6RetalLys" EXACT PSI-MOD-label []
-synonym: "retinal" RELATED Unimod-description []
-synonym: "Retinylidene" RELATED PSI-MS-label []
-property_value: DiffAvg "266.43" xsd:float
-property_value: DiffFormula "C 20 H 26 N 0 O 0" xsd:string
-property_value: DiffMono "266.203451" xsd:float
-property_value: Formula "C 26 H 38 N 2 O 1" xsd:string
-property_value: MassAvg "394.60" xsd:float
-property_value: MassMono "394.298414" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:380
-xref: uniprot.ptm:PTM-0388
-is_a: MOD:00912
-
-[Term]
-id: MOD:00130
-name: L-allysine
-def: "A protein modification that effectively converts an L-lysine residue to L-allysine." [ChEBI:17917, DeltaMass:0, PubMed:11120890, PubMed:11332453, PubMed:358196, PubMed:5337886, PubMed:5529814, RESID:AA0121, Unimod:352#K]
-comment: From DeltaMass: Average Mass: -1
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-6-oxohexanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-5-formylvaleric acid" EXACT RESID-alternate []
-synonym: "2-amino-adipic acid semialdahyde" EXACT RESID-alternate []
-synonym: "2-aminoadipate 6-semialdehyde" EXACT RESID-alternate []
-synonym: "5-formyl-norvaline" EXACT RESID-alternate []
-synonym: "6-oxonorleucine" EXACT RESID-alternate []
-synonym: "AASA" EXACT RESID-alternate []
-synonym: "Allysine (from Lysine)" EXACT DeltaMass-label []
-synonym: "alpha-amino-adipic acid delta-semialdahyde" EXACT RESID-alternate []
-synonym: "L-allysine" EXACT RESID-name []
-synonym: "Lys->Allysine" RELATED PSI-MS-label []
-synonym: "Lysal" EXACT PSI-MOD-label []
-synonym: "Lysine oxidation to aminoadipic semialdehyde" RELATED Unimod-description []
-synonym: "MOD_RES Allysine" EXACT UniProt-feature []
-synonym: "Oxidation of lysine (to aminoadipic semialdehyde)" EXACT DeltaMass-label []
-property_value: DiffAvg "-1.03" xsd:float
-property_value: DiffFormula "C 0 H -3 N -1 O 1" xsd:string
-property_value: DiffMono "-1.031634" xsd:float
-property_value: Formula "C 6 H 9 N 1 O 2" xsd:string
-property_value: MassAvg "127.14" xsd:float
-property_value: MassMono "127.063329" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:352
-xref: uniprot.ptm:PTM-0059
-is_a: MOD:00912
-
-[Term]
-id: MOD:00131
-name: L-2-aminoadipic acid
-def: "A protein modification that effectively converts an L-lysine residue to L-2-aminoadipic acid." [DeltaMass:353, PubMed:336041, PubMed:358196, PubMed:7419498, RESID:AA0122, Unimod:381#K]
-comment: From DeltaMass: References:Amici A, Levine, RL, Tsai, L, and Stadtman, ER: Conversion of amino acid residues in proteins and amino acid homopolymers to carbonyl derivatives by metal-catalyzed oxidation reactions. Journal of Biological Chemistry 264: 3341-3346 1989.Requena JR, Chao CC, Levine RL, and Stadtman ER: Glutamic and aminoadipic semialdehydes are the main carbonyl products of metal-catalyzed oxidation of proteins. Proceedings of the National Academy of Sciences USA 98: 69-74 2001. Notes:Expected reaction following oxidation of lysine to aminoadipic semialdehyde. Not proven experimentally but deduced by reference to the similar known reaction of oxidation of Arg to Glu via the semialdehyde. [This has been observed as a natural modification, see RESID:AA0122. JSG]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-aminohexanedioic acid" EXACT RESID-systematic []
-synonym: "2-amino-1,4-butanedicarboxylic acid" EXACT RESID-alternate []
-synonym: "alpha-amino adipic acid" RELATED Unimod-description []
-synonym: "L-2-aminoadipic acid" EXACT RESID-name []
-synonym: "L-alpha-aminoadipic acid" EXACT RESID-alternate []
-synonym: "Lys->AminoadipicAcid" RELATED PSI-MS-label []
-synonym: "Lysoic" EXACT PSI-MOD-label []
-synonym: "Oxidation of lysine (to aminoadipic acid)" EXACT DeltaMass-label []
-property_value: DiffAvg "14.97" xsd:float
-property_value: DiffFormula "C 0 H -3 N -1 O 2" xsd:string
-property_value: DiffMono "14.963280" xsd:float
-property_value: Formula "C 6 H 9 N 1 O 3" xsd:string
-property_value: MassAvg "143.14" xsd:float
-property_value: MassMono "143.058243" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:381
-is_a: MOD:00912
-
-[Term]
-id: MOD:00132
-name: L-lysinoalanine (Lys-Ser)
-def: "A protein modification that effectively crosslinks an L-serine residue and an L-lysine residue to release water and form 2-amino-6-(2-amino-2-carboxyethylamino)hexanoic acid." [DeltaMass:0, PubMed:2544544, RESID:AA0123#KSX]
-comment: Cross-link 2. This entry is for the crosslink of peptidyl serine and peptidyl lysine. For the modification of peptidyl lysine by a free serine see MOD:01838. From DeltaMass: Average Mass: -34.
-synonym: "(2R,9S)-lysinoalanine" EXACT RESID-alternate []
-synonym: "(2S)-2-amino-6-([(2R)-2-amino-2-carboxyethyl]amino)hexanoic acid" EXACT RESID-systematic []
-synonym: "alaninolysine" EXACT RESID-alternate []
-synonym: "CROSSLNK Lysinoalanine (Ser-Lys)" EXACT UniProt-feature []
-synonym: "L-lysinoalanine" EXACT RESID-name []
-synonym: "LAL" EXACT RESID-alternate []
-synonym: "Lysinoalanine (from Cysteine)" EXACT DeltaMass-label []
-synonym: "N-epsilon-(2-amino-2-carboxyethyl)-L-lysine" EXACT RESID-alternate []
-synonym: "N6-(2-amino-2-carboxyethyl)-L-lysine" EXACT RESID-alternate []
-synonym: "XLNK-N6Lys-3Dha(Ser)" EXACT PSI-MOD-label []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 9 H 15 N 3 O 2" xsd:string
-property_value: MassAvg "197.24" xsd:float
-property_value: MassMono "197.116427" xsd:float
-property_value: Origin "K, S" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0172
-is_a: MOD:02055
-is_a: MOD:02051
-is_a: MOD:00954
-is_a: MOD:01853
-
-[Term]
-id: MOD:00133
-name: N6-(L-isoglutamyl)-L-lysine (Gln)
-def: "A protein modification that effectively crosslinks an L-glutamine residue and an L-lysine residue by an isopeptide bond with the formation of N6-(L-isoglutamyl)-L-lysine and the release of ammonia." [ChEBI:21863, DeltaMass:0, PubMed:2461365, PubMed:5637041, PubMed:5656070, PubMed:8598899, RESID:AA0124#GLN]
-comment: Cross-link 2.
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-6-([(4S)-4-amino-4-carboxybutanoyl]amino)hexanoic acid" EXACT RESID-systematic []
-synonym: "2-azanyl-6-([4-azanyl-4-carboxybutanoyl]azanyl)hexanoic acid" EXACT RESID-alternate []
-synonym: "5-glutamyl N6-lysine" EXACT RESID-alternate []
-synonym: "CROSSLNK Isoglutamyl lysine isopeptide (Lys-Gln)" EXACT UniProt-feature []
-synonym: "N alpha -(gamma-Glutamyl)-lysine" EXACT DeltaMass-label []
-synonym: "N(epsilon)-(gamma-glutamyl)lysine" EXACT RESID-alternate []
-synonym: "N6-(L-isoglutamyl)-L-lysine" EXACT RESID-name []
-synonym: "XLNK-N6Lys-5Glu(Gln)" EXACT PSI-MOD-label []
-property_value: DiffAvg "-17.03" xsd:float
-property_value: DiffFormula "C 0 H -3 N -1 O 0" xsd:string
-property_value: DiffMono "-17.026549" xsd:float
-property_value: Formula "C 11 H 17 N 3 O 3" xsd:string
-property_value: MassAvg "239.27" xsd:float
-property_value: MassMono "239.126991" xsd:float
-property_value: Origin "K, Q" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0158
-is_a: MOD:02046
-is_a: MOD:00946
-is_a: MOD:01630
-
-[Term]
-id: MOD:00134
-name: N6-glycyl-L-lysine
-def: "A protein modification that effectively crosslinks an L-lysine residue and a glycine residue by an isopeptide bond to form N6-glycyl-L-lysine." [ChEBI:21885, RESID:AA0125]
-comment: Cross-link 2; this is the common crosslink structure formed by ubiquitin, SUMO, and similar proteins.
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-6-[(aminoacetyl)amino]hexanoic acid" EXACT RESID-systematic []
-synonym: "N6-(glycyl)-L-lysine" EXACT RESID-name []
-synonym: "N6-glycyllysine" EXACT RESID-alternate []
-synonym: "XLNK-N6Lys-1Gly" EXACT PSI-MOD-label []
-synonym: "CROSSLNK Glycyl lysine isopeptide (Gly-Lys) (interchain with K-...)" EXACT UniProt-feature []
-synonym: "CROSSLNK Glycyl lysine isopeptide (Lys-Gly) (interchain with G-...)" EXACT UniProt-feature []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 8 H 14 N 3 O 2" xsd:string
-property_value: MassAvg "184.22" xsd:float
-property_value: MassMono "184.108602" xsd:float
-property_value: Origin "G, K" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0134
-is_a: MOD:00688
-is_a: MOD:02047
-is_a: MOD:02051
-is_a: MOD:00954
-is_a: MOD:01875
-
-[Term]
-id: MOD:00135
-name: N-(L-isoaspartyl)-glycine (Asn)
-def: "A protein modification that effectively crosslinks an L-asparagine residue and a glycine residue by an isopeptide bond with formation of N-(L-isoaspartyl)glycine and the release of ammonia." [ChEBI:21479, PubMed:1826288, RESID:AA0126]
-comment: Cross-link 2.
-synonym: "(2S)-2-amino-4-(carboxymethyl)amino-4-oxobutanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-N4-(carboxymethyl)-butanediamic acid" EXACT RESID-alternate []
-synonym: "CROSSLNK Isoaspartyl glycine isopeptide (Asn-Gly)" EXACT UniProt-feature []
-synonym: "CROSSLNK Isoaspartyl glycine isopeptide (Gly-Asn)" EXACT UniProt-feature []
-synonym: "isoaspartyl glycine" EXACT RESID-alternate []
-synonym: "N-(L-isoaspartyl)-glycine" EXACT RESID-name []
-synonym: "N-beta-aspartylglycine" EXACT RESID-alternate []
-synonym: "N4-(carboxymethyl)-asparagine" EXACT RESID-alternate []
-synonym: "XLNK-4Asp-NGly(Asn)" EXACT PSI-MOD-label []
-property_value: DiffAvg "-17.03" xsd:float
-property_value: DiffFormula "C 0 H -3 N -1 O 0" xsd:string
-property_value: DiffMono "-17.026549" xsd:float
-property_value: Formula "C 6 H 7 N 2 O 3" xsd:string
-property_value: MassAvg "155.13" xsd:float
-property_value: MassMono "155.045667" xsd:float
-property_value: Origin "G, N" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0489
-is_a: MOD:02042
-is_a: MOD:00946
-is_a: MOD:01928
-
-[Term]
-id: MOD:00136
-name: pyruvic acid (Cys)
-def: "A protein modification that effectively converts an L-cysteine residue to pyruvic acid." [PubMed:10085076, PubMed:3042771, PubMed:8464063, RESID:AA0127#CYS, Unimod:382]
-subset: PSI-MOD-slim
-synonym: "2-oxopropanoic acid" EXACT RESID-systematic []
-synonym: "MOD_RES Pyruvic acid (Cys)" EXACT UniProt-feature []
-synonym: "Pyruv(Cys)" EXACT PSI-MOD-label []
-synonym: "pyruvic acid" EXACT RESID-name []
-property_value: DiffAvg "-33.09" xsd:float
-property_value: DiffFormula "C 0 H -3 N -1 O 1 S -1" xsd:string
-property_value: DiffMono "-33.003705" xsd:float
-property_value: Formula "C 3 H 3 O 2" xsd:string
-property_value: MassAvg "71.06" xsd:float
-property_value: MassMono "71.013304" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:382
-xref: uniprot.ptm:PTM-0265
-is_a: MOD:00905
-is_a: MOD:01154
-
-[Term]
-id: MOD:00137
-name: L-3-phenyllactic acid
-def: "A protein modification that effectively converts an L-phenylalanine residue into L-3-phenyllactic acid." [PubMed:1973541, RESID:AA0128, Unimod:7#F]
-comment: This modification is not the result of deamidation, instead the alpha amino group is replaced with an hydroxyl group.
-synonym: "(2S)-2-hydroxy-3-phenylpropanoic acid" EXACT RESID-systematic []
-synonym: "Deamidated" RELATED Unimod-interim []
-synonym: "Deamidation" RELATED Unimod-description []
-synonym: "L-3-phenyllactic acid" EXACT RESID-name []
-synonym: "MOD_RES 3-phenyllactic acid" EXACT UniProt-feature []
-property_value: DiffAvg "0.98" xsd:float
-property_value: DiffFormula "C 0 H -1 N -1 O 1" xsd:string
-property_value: DiffMono "0.984016" xsd:float
-property_value: Formula "C 9 H 9 O 2" xsd:string
-property_value: MassAvg "149.17" xsd:float
-property_value: MassMono "149.060255" xsd:float
-property_value: Origin "F" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:7
-xref: uniprot.ptm:PTM-0035
-is_a: MOD:00914
-
-[Term]
-id: MOD:00138
-name: 2-oxobutanoic acid
-def: "A protein modification that effectively converts an L-threonine residue into 2-oxobutanoic acid." [PubMed:15023056, PubMed:1680314, PubMed:2253617, PubMed:2764678, RESID:AA0129, Unimod:385#T, ChEBI:149508]
-synonym: "2-ketobutyric acid" EXACT RESID-alternate []
-synonym: "2-oxobutanoic acid" EXACT RESID-name []
-synonym: "2-oxobutanoic acid" EXACT RESID-systematic []
-synonym: "2-oxobutyric acid" EXACT RESID-alternate []
-synonym: "Ammonia-loss" RELATED Unimod-interim []
-synonym: "Loss of ammonia" RELATED Unimod-description []
-synonym: "MOD_RES 2-oxobutanoic acid" EXACT UniProt-feature []
-property_value: DiffAvg "-17.03" xsd:float
-property_value: DiffFormula "C 0 H -3 N -1 O 0" xsd:string
-property_value: DiffMono "-17.026549" xsd:float
-property_value: Formula "C 4 H 5 O 2" xsd:string
-property_value: MassAvg "85.08" xsd:float
-property_value: MassMono "85.028954" xsd:float
-property_value: Origin "T" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:385
-xref: uniprot.ptm:PTM-0017
-is_a: MOD:00917
-is_a: MOD:01160
-
-[Term]
-id: MOD:00139
-name: N2-succinyl-L-tryptophan
-def: "A protein modification that effectively converts an L-tryptophan residue to N2-succinyl-L-tryptophan." [PubMed:11857757, PubMed:12175151, PubMed:8471040, RESID:AA0130, Unimod:64#N-term]
-synonym: "(2S)-2-(3-carboxypropanoyl)amino-3-(1H-indol-3-yl)propanoic acid" EXACT RESID-systematic []
-synonym: "(2S)-2-amino-(6,7-dihydro-6,7-dioxo-1H-indole)-3-propanoic acid" EXACT RESID-alternate []
-synonym: "MOD_RES N2-succinyltryptophan" EXACT UniProt-feature []
-synonym: "N2-succinyl-L-tryptophan" EXACT RESID-name []
-synonym: "Succinic anhydride labeling reagent light form (N-term)" RELATED Unimod-description []
-synonym: "Succinyl" RELATED PSI-MS-label []
-property_value: DiffAvg "100.07" xsd:float
-property_value: DiffFormula "C 4 H 4 N 0 O 3" xsd:string
-property_value: DiffMono "100.016044" xsd:float
-property_value: Formula "C 15 H 15 N 2 O 4" xsd:string
-property_value: MassAvg "287.29" xsd:float
-property_value: MassMono "287.103182" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:64
-xref: uniprot.ptm:PTM-0181
-is_a: MOD:02081
-is_a: MOD:00918
-
-[Term]
-id: MOD:00140
-name: S-phycocyanobilin-L-cysteine
-def: "A protein modification that effectively results from forming an adduct between a cysteine residue and the tetrapyrrole compound phycocyanobilin." [ChEBI:15617, DeltaMass:0, PubMed:16644722, PubMed:3208761, PubMed:3838747, PubMed:7918400, RESID:AA0131, Unimod:387#C]
-comment: From DeltaMass: Average Mass: 587.
-synonym: "(2R,3R)-3-[(1R)-1-(((2R)-2-amino-2-carboxy)ethylsulfanyl)ethyl]-18-ethyl-1,2,3,19,21,22,24-heptahydro-2,7,13,17-tetramethyl-1,19-dioxo-(21H,22H,24H)-bilin-8,12-dipropanoic acid" EXACT RESID-alternate []
-synonym: "(2R,3R)-3-[(1R)-1-(((2R)-2-amino-2-carboxy)ethylsulfanyl)ethyl]-8,12-bis(2-carboxyethyl)-18-ethyl-2,7,13,17-tetramethyl-1,2,3,19,21,22,24-heptahydrobilin-1,19(21H,22H,24H)-dione" EXACT RESID-systematic []
-synonym: "BINDING Phycocyanobilin chromophore (covalent; via 1 link)" EXACT UniProt-feature []
-synonym: "PCB" EXACT RESID-alternate []
-synonym: "phycobilin cysteine" EXACT RESID-alternate []
-synonym: "Phycocyanobilin" RELATED PSI-MS-label []
-synonym: "phycocyanobilin" RELATED Unimod-description []
-synonym: "phycocyanobilin cysteine adduct" EXACT RESID-alternate []
-synonym: "S-Phycocyanobilin (on Cysteine)" EXACT DeltaMass-label []
-synonym: "S-phycocyanobilin-L-cysteine" EXACT RESID-name []
-property_value: DiffAvg "586.69" xsd:float
-property_value: DiffFormula "C 33 H 38 N 4 O 6 S 0" xsd:string
-property_value: DiffMono "586.279135" xsd:float
-property_value: Formula "C 36 H 43 N 5 O 7 S 1" xsd:string
-property_value: MassAvg "689.83" xsd:float
-property_value: MassMono "689.288320" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:387
-is_a: MOD:00700
-is_a: MOD:00905
-
-[Term]
-id: MOD:00141
-name: S-phycoerythrobilin-L-cysteine
-def: "A protein modification that effectively results from forming an adduct between a cysteine residue and the tetrapyrrole compound phycoerythrobilin." [ChEBI:15618, PubMed:14588022, PubMed:3208761, PubMed:3838747, PubMed:8876649, RESID:AA0132, Unimod:388#C]
-synonym: "(2S,3R,16R)-18-ethenyl-3-[(1R)-1-(((2R)-2-amino-2-carboxy)ethylsulfanyl)ethyl]-8,12-bis(2-carboxyethyl)-2,7,13,17-tetramethyl-2,3,15,16-tetrahydrobilin-1,19(21H,22H,24H)-dione" EXACT RESID-systematic []
-synonym: "18-ethenyl-3-[1-((2-amino-2-carboxy)ethylsulfanyl)ethyl]-2,3,15,16-tetrahydro-2,7,13,17-tetramethyl-1,19-dioxo-(21H,22H,24H)-bilin-8,12-dipropanoic acid" EXACT RESID-alternate []
-synonym: "BINDING Phycoerythrobilin chromophore (covalent; via 1 link)" EXACT UniProt-feature []
-synonym: "PEB" EXACT RESID-alternate []
-synonym: "Phycoerythrobilin" RELATED PSI-MS-label []
-synonym: "phycoerythrobilin" RELATED Unimod-description []
-synonym: "phycoerythrobilin cysteine adduct" EXACT RESID-alternate []
-synonym: "S-phycoerythrobilin-L-cysteine" EXACT RESID-name []
-property_value: DiffAvg "588.70" xsd:float
-property_value: DiffFormula "C 33 H 40 N 4 O 6 S 0" xsd:string
-property_value: DiffMono "588.294785" xsd:float
-property_value: Formula "C 36 H 45 N 5 O 7 S 1" xsd:string
-property_value: MassAvg "691.84" xsd:float
-property_value: MassMono "691.303970" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:388
-is_a: MOD:00700
-is_a: MOD:00905
-
-[Term]
-id: MOD:00142
-name: S-phytochromobilin-L-cysteine
-def: "A protein modification that effectively results from forming an adduct between a cysteine residue and the tetrapyrrole compound phytochromobilin." [ChEBI:15619, PubMed:1634523, PubMed:16593380, PubMed:3208761, PubMed:7918400, RESID:AA0133, Unimod:389#C]
-synonym: "(2R,3R)-3-[(1R)-1-(((2R)-2-amino-2-carboxy)ethylsulfanyl)ethyl]-8,12-bis(2-carboxyethyl)-18-ethyl-2,7,13,17-tetramethyl-1,2,3,19,21,22,24-heptahydrobilin-1,19(21H,22H,24H)-dione" EXACT RESID-systematic []
-synonym: "18-ethenyl-3-[1-((2-amino-2-carboxy)ethylsulfanyl)ethyl]-1,2,3,19,22,24-hexahydro-2,7,13,17-tetramethyl-1,19-dioxo-21H-biline-8,12-dipropanoic acid" EXACT RESID-alternate []
-synonym: "BINDING Phytochromobilin chromophore (covalent; via 1 link)" EXACT UniProt-feature []
-synonym: "phytochrome chromophore" EXACT RESID-alternate []
-synonym: "Phytochromobilin" RELATED PSI-MS-label []
-synonym: "phytochromobilin" RELATED Unimod-description []
-synonym: "phytochromobilin cysteine adduct" EXACT RESID-alternate []
-synonym: "S-phytochromobilin-L-cysteine" EXACT RESID-name []
-property_value: DiffAvg "584.67" xsd:float
-property_value: DiffFormula "C 33 H 36 N 4 O 6 S 0" xsd:string
-property_value: DiffMono "584.263485" xsd:float
-property_value: Formula "C 36 H 41 N 5 O 7 S 1" xsd:string
-property_value: MassAvg "687.81" xsd:float
-property_value: MassMono "687.272670" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:389
-is_a: MOD:00700
-is_a: MOD:00905
-
-[Term]
-id: MOD:00143
-name: heme-bis-L-cysteine
-def: "A protein modification that effectively results from forming an adduct between two cysteine residues and the porphyrin compound heme b, (7,12-diethenyl-3,8,13,17-tetramethylporphyrin-2,18-dipropanoato)iron." [ChEBI:17627, PubMed:5545094, PubMed:8827449, RESID:AA0134]
-comment: Cross-link 2.
-subset: PSI-MOD-slim
-synonym: "(7,12-bis[(1S)-1-([(2R)-2-amino-2-carboxyethyl]sulfanyl)ethyl]-3,8,13,17-tetramethyl-21H,23H-porphine-2,18-bis[2-carboxyethyl]-N21,N22,N23,N24)-ferrate" EXACT RESID-systematic []
-synonym: "2,4-bis[1-(S-cysteinyl)ethyl]protoporphyrin IX" EXACT RESID-alternate []
-synonym: "BINDING Heme (covalent)" EXACT UniProt-feature []
-synonym: "biscysteinyl heme" EXACT RESID-alternate []
-synonym: "heme-bis-L-cysteine" EXACT RESID-name []
-synonym: "HemeCys2" EXACT PSI-MOD-label []
-property_value: DiffAvg "616.50" xsd:float
-property_value: DiffFormula "C 34 Fe 1 H 32 N 4 O 4 S 0" xsd:string
-property_value: DiffMono "616.177293" xsd:float
-property_value: Formula "C 40 Fe 1 H 42 N 6 O 6 S 2" xsd:string
-property_value: MassAvg "822.78" xsd:float
-property_value: MassMono "822.195663" xsd:float
-property_value: Origin "C, C" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00699
-is_a: MOD:02067
-
-[Term]
-id: MOD:00144
-name: heme-L-cysteine
-def: "A protein modification that effectively results from forming an adduct between a cysteine residue and the porphyrin compound heme b, (7,12-diethenyl-3,8,13,17-tetramethylporphyrin-2,18-dipropanoato)iron." [ChEBI:17627, DeltaMass:0, PubMed:170910, PubMed:192772, PubMed:2536325, PubMed:9535866, RESID:AA0135, Unimod:390#C]
-comment: From DeltaMass: Average Mass: 617.
-subset: PSI-MOD-slim
-synonym: "(12-ethenyl-7-[(1S)-1-([(2R)-2-amino-2-carboxyethyl]sulfanyl)ethyl]-3,8,13,17-tetramethyl-21H,23H-porphine-2,18-bis[2-carboxyethyl]-N21,N22,N23,N24)-ferrate" EXACT RESID-systematic []
-synonym: "4-[1-(S-cysteinyl)ethyl]protoporphyrin IX" EXACT RESID-alternate []
-synonym: "BINDING Heme (covalent; via 1 link)" EXACT UniProt-feature []
-synonym: "cysteinyl heme" EXACT RESID-alternate []
-synonym: "Heme" RELATED PSI-MS-label []
-synonym: "heme" RELATED Unimod-description []
-synonym: "heme-L-cysteine" EXACT RESID-name []
-synonym: "HemeCys1" EXACT PSI-MOD-label []
-synonym: "S-Heme (on Cysteine)" EXACT DeltaMass-label []
-property_value: DiffAvg "616.50" xsd:float
-property_value: DiffFormula "C 34 Fe 1 H 32 N 4 O 4 S 0" xsd:string
-property_value: DiffMono "616.177293" xsd:float
-property_value: Formula "C 37 Fe 1 H 37 N 5 O 5 S 1" xsd:string
-property_value: MassAvg "719.64" xsd:float
-property_value: MassMono "719.186478" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:390
-is_a: MOD:00699
-is_a: MOD:02067
-
-[Term]
-id: MOD:00145
-name: tetrakis-L-cysteinyl iron
-def: "A protein modification that effectively converts four L-cysteine residues iron atom to tetrakis-L-cysteinyl iron." [PubMed:1303768, PubMed:2244884, RESID:AA0136]
-comment: Cross-link 4.
-synonym: "METAL Iron" EXACT UniProt-feature []
-synonym: "tetrakis(cysteinato-kappaS)-iron" EXACT RESID-systematic []
-synonym: "tetrakis-L-cysteinyl iron" EXACT RESID-name []
-property_value: DiffAvg "51.81" xsd:float
-property_value: DiffFormula "C 0 Fe 1 H -4 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "51.904735" xsd:float
-property_value: FormalCharge "2-" xsd:string
-property_value: Formula "C 12 Fe 1 H 16 N 4 O 4 S 4" xsd:string
-property_value: MassAvg "464.37" xsd:float
-property_value: MassMono "463.941474" xsd:float
-property_value: Origin "C, C, C, C" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00738
-is_a: MOD:02067
-
-[Term]
-id: MOD:00146
-name: tetrakis-L-cysteinyl diiron disulfide
-def: "A protein modification that effectively converts four L-cysteine residues and a two-iron two-sulfur cluster to tetrakis-L-cysteinyl diiron disulfide." [PubMed:2123937, PubMed:6801028, PubMed:7763242, PubMed:8688437, RESID:AA0137]
-comment: Cross-link 4.
-synonym: "METAL Iron-sulfur (2Fe-2S)" EXACT UniProt-feature []
-synonym: "METAL Iron-sulfur (2Fe-2S); shared with dimeric partner" EXACT UniProt-feature []
-synonym: "tetrakis-L-cysteinyl diiron disulfide" EXACT RESID-name []
-synonym: "tetrakiscysteinato-1kappa(2)S,2kappa(2)S-di-mu-sulfido-diiron" EXACT RESID-systematic []
-property_value: DiffAvg "171.78" xsd:float
-property_value: DiffFormula "C 0 Fe 2 H -4 N 0 O 0 S 2" xsd:string
-property_value: DiffMono "171.783814" xsd:float
-property_value: FormalCharge "2-" xsd:string
-property_value: Formula "C 12 Fe 2 H 16 N 4 O 4 S 6" xsd:string
-property_value: MassAvg "584.34" xsd:float
-property_value: MassMono "583.820553" xsd:float
-property_value: Origin "C, C, C, C" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00739
-is_a: MOD:02067
-
-[Term]
-id: MOD:00147
-name: hexakis-L-cysteinyl triiron trisulfide
-def: "A protein modification that effectively converts six L-cysteine residues and a three-iron three-sulfur cluster to hexakis-L-cysteinyl triiron trisulfide." [PubMed:3379067, PubMed:3932661, PubMed:7354058, RESID:AA0138]
-comment: Cross-link 6. This is a deprecated entry in RESID. It probably does not occur naturally [JSG].
-synonym: "hexakis-L-cysteinyl triiron trisulfide" EXACT RESID-name []
-synonym: "tri-mu-sulfido-hexakiscysteinato-1kappa(2)S,2kappa(2)S,3kappa(2)S-triiron" EXACT RESID-systematic []
-synonym: "tri-mu-sulfidotris(biscysteinato-kappaS-iron)" EXACT RESID-alternate []
-property_value: DiffAvg "257.67" xsd:float
-property_value: DiffFormula "C 0 Fe 3 H -6 N 0 O 0 S 3" xsd:string
-property_value: DiffMono "257.675721" xsd:float
-property_value: FormalCharge "3-" xsd:string
-property_value: Formula "C 18 Fe 3 H 24 N 6 O 6 S 9" xsd:string
-property_value: MassAvg "876.50" xsd:float
-property_value: MassMono "875.730830" xsd:float
-property_value: Origin "C, C, C, C, C, C" xsd:string
-property_value: Source "hypothetical" xsd:string
-is_a: MOD:00739
-is_a: MOD:02067
-
-[Term]
-id: MOD:00148
-name: tris-L-cysteinyl triiron tetrasulfide
-def: "A protein modification that effectively converts three L-cysteine residues and a three-iron four-sulfur cluster to tris-L-cysteinyl triiron tetrasulfide." [PubMed:10555576, PubMed:2056535, PubMed:3422475, PubMed:6848518, PubMed:7819255, PubMed:9063899, RESID:AA0139]
-comment: Cross-link 3.
-synonym: "METAL Iron-sulfur (3Fe-4S)" EXACT UniProt-feature []
-synonym: "mu3-sulfido tri-mu-sulfido tris-S-L-cysteinyl triiron" EXACT RESID-alternate []
-synonym: "mu3-sulfido-tri-mu-sulfido-triscysteinato-1kappaS,2kappaS,3kappaS-triiron" EXACT RESID-systematic []
-synonym: "tris-L-cysteinyl triiron tetrasulfide" EXACT RESID-name []
-synonym: "tris-L-cysteinyl triiron tetrasulfide C3 cluster" EXACT RESID-alternate []
-synonym: "tris-L-cysteinyl triiron tetrasulfide cubane form" EXACT RESID-alternate []
-synonym: "tris-L-cysteinyl triiron tetrasulfide cuboid cluster" EXACT RESID-alternate []
-synonym: "tris-L-cysteinyl triiron tetrasulfide trigonal cluster" EXACT RESID-alternate []
-property_value: DiffAvg "292.75" xsd:float
-property_value: DiffFormula "C 0 Fe 3 H -3 N 0 O 0 S 4" xsd:string
-property_value: DiffMono "292.671267" xsd:float
-property_value: FormalCharge "3-" xsd:string
-property_value: Formula "C 9 Fe 3 H 12 N 3 O 3 S 7" xsd:string
-property_value: MassAvg "602.17" xsd:float
-property_value: MassMono "601.698821" xsd:float
-property_value: Origin "C, C, C" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00739
-is_a: MOD:02067
-
-[Term]
-id: MOD:00149
-name: tetrakis-L-cysteinyl tetrairon tetrasulfide
-def: "A protein modification that effectively converts four L-cysteine residues and a four-iron four-sulfur cluster to tetrakis-L-cysteinyl tetrairon tetrasulfide." [PubMed:3351918, PubMed:7803404, PubMed:7819196, PubMed:932007, RESID:AA0140]
-comment: Cross-link 4.
-synonym: "METAL Iron-sulfur (4Fe-4S)" EXACT UniProt-feature []
-synonym: "METAL Iron-sulfur (4Fe-4S); shared with dimeric partner" EXACT UniProt-feature []
-synonym: "tetra-mu3-sulfido-tetrakis(cysteinato)-1kappaS,2kappaS,3kappaS,4kappaS-tetrahedro-tetrairon" EXACT RESID-systematic []
-synonym: "tetra-mu3-sulfidotetrakis(S-cysteinyliron)" EXACT RESID-alternate []
-synonym: "tetrakis-L-cysteinyl tetrairon tetrasulfide" EXACT RESID-name []
-property_value: DiffAvg "347.59" xsd:float
-property_value: DiffFormula "C 0 Fe 4 H -4 N 0 O 0 S 4" xsd:string
-property_value: DiffMono "347.597831" xsd:float
-property_value: FormalCharge "2-" xsd:string
-property_value: Formula "C 12 Fe 4 H 16 N 4 O 4 S 8" xsd:string
-property_value: MassAvg "760.15" xsd:float
-property_value: MassMono "759.634570" xsd:float
-property_value: Origin "C, C, C, C" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00739
-is_a: MOD:02067
-
-[Term]
-id: MOD:00150
-name: L-cysteinyl-L-histidino-homocitryl molybdenum heptairon nonasulfide
-def: "A protein modification that effectively converts an L-cysteine residue, an L-histidine residue, homocitric acid and a one-molybdenum seven-iron nine-sulfur cluster to L-cysteinyl-L-histidino-homocitryl molybdenum heptairon nonasulfide." [PubMed:10525412, PubMed:12215645, PubMed:12733878, PubMed:1529354, PubMed:8027059, RESID:AA0141]
-comment: Cross-link 2; incidental to RESID:AA0300.
-synonym: "cysteinato-8kappaS-histidino-1kappaN(tau)-[(2R)-4-carboxy-2-(carboxymethyl)-2-oxidobutanoate-1kappaO(1),1kappaO(2)]-mu6-carbido-2:3:4:5:6:7kappa(6)C-hexa-mu3-sulfido-1:2:3kappa(3)S;1:2:4kappa(3)S;1:3:4kappa(3)S;5:6:8kappa(3)S;5:7:8kappa(3)S;6:7:8kappa(3)S-tri-mu2-sulfido-2:5kappa(2)S;3:6kappa(2)S;4:7kappa(2)S molybdenum heptairon" EXACT RESID-systematic []
-synonym: "L-cysteinyl-L-histidino-homocitryl molybdenum heptairon nonasulfide carbide" EXACT RESID-name []
-synonym: "nitrogenase iron-molybdenum cofactor" EXACT RESID-alternate []
-property_value: DiffAvg "991.53" xsd:float
-property_value: DiffFormula "C 7 Fe 7 H 6 Mo 1 N 1 O 7 S 9" xsd:string
-property_value: DiffMono "993.213036" xsd:float
-property_value: Formula "C 16 Fe 7 H 18 Mo 1 N 5 O 9 S 10" xsd:string
-property_value: MassAvg "1231.81" xsd:float
-property_value: MassMono "1233.281133" xsd:float
-property_value: Origin "C, H" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00739
-is_a: MOD:00743
-is_a: MOD:02067
-is_a: MOD:02070
-
-[Term]
-id: MOD:00151
-name: L-cysteinyl molybdopterin
-def: "A protein modification that effectively converts an L-cysteine residue to L-cysteinyl molybdopterin." [PubMed:14527393, PubMed:7878465, PubMed:9428520, RESID:AA0142, Unimod:391#C]
-subset: PSI-MOD-slim
-synonym: "(4R,5aR,11aR)-8-amino-2-[(2R)-2-amino-2-carboxyethyl]sulfanyl-4,5a,6,9,10,11,11a-heptahydro-4-(phosphoric acid)methyl-2,2,10-trioxo-pteridino[6,7-5,6]pyrano[3,4-4,3][1,2,5]molybdadithiolene" EXACT RESID-systematic []
-synonym: "cysteinyl Mo-molybdopterin" EXACT RESID-alternate []
-synonym: "cysteinyl Mo-pterin" EXACT RESID-alternate []
-synonym: "L-cysteinyl molybdopterin" EXACT RESID-name []
-synonym: "METAL Molybdenum-pterin" EXACT UniProt-feature []
-synonym: "molybdoenzyme molybdenum cofactor" EXACT RESID-alternate []
-synonym: "Molybdopterin" RELATED PSI-MS-label []
-synonym: "molybdopterin" RELATED Unimod-description []
-synonym: "MoPterCys" EXACT PSI-MOD-label []
-property_value: DiffAvg "520.27" xsd:float
-property_value: DiffFormula "C 10 H 11 Mo 1 N 5 O 8 P 1 S 2" xsd:string
-property_value: DiffMono "521.884074" xsd:float
-property_value: Formula "C 13 H 16 Mo 1 N 6 O 9 P 1 S 3" xsd:string
-property_value: MassAvg "623.41" xsd:float
-property_value: MassMono "624.893259" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:391
-is_a: MOD:00744
-is_a: MOD:00861
-is_a: MOD:02067
-
-[Term]
-id: MOD:00152
-name: S-(8alpha-FAD)-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S'-(8alpha-FAD)-L-cystine." [PubMed:10220347, RESID:AA0143, Unimod:50#C]
-subset: PSI-MOD-slim
-synonym: "(2R)-2-amino-3-[8alpha-riboflavin 5'-(trihydrogen diphosphate) 5'->5'-ester with adenosine]sulfanylpropanoic acid" EXACT RESID-systematic []
-synonym: "8alpha-(S-cysteinyl)FAD" EXACT RESID-alternate []
-synonym: "FAD" RELATED PSI-MS-label []
-synonym: "Flavin adenine dinucleotide" RELATED Unimod-description []
-synonym: "MOD_RES S-8alpha-FAD cysteine" EXACT UniProt-feature []
-synonym: "S-(8alpha-FAD)-L-cysteine" EXACT RESID-name []
-synonym: "S8aFADCys" EXACT PSI-MOD-label []
-property_value: DiffAvg "783.54" xsd:float
-property_value: DiffFormula "C 27 H 31 N 9 O 15 P 2 S 0" xsd:string
-property_value: DiffMono "783.141485" xsd:float
-property_value: Formula "C 30 H 36 N 10 O 16 P 2 S 1" xsd:string
-property_value: MassAvg "886.68" xsd:float
-property_value: MassMono "886.150669" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:50
-xref: uniprot.ptm:PTM-0272
-is_a: MOD:00895
-is_a: MOD:00905
-
-[Term]
-id: MOD:00153
-name: 3'-(8alpha-FAD)-L-histidine
-def: "A protein modification that effectively converts an L-histidine residue to 3'-(8alpha-FAD)-L-histidine." [PubMed:241294, PubMed:8076, RESID:AA0144, Unimod:50#H]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-(3-[8alpha-riboflavin 5'-(trihydrogen diphosphate) 5'->5'-ester with adenosine]imidazol-4-yl)propanoic acid" EXACT RESID-systematic []
-synonym: "3'-(8alpha-FAD)-L-histidine" EXACT RESID-name []
-synonym: "8alpha-(N(delta)-histidyl)FAD" EXACT RESID-alternate []
-synonym: "8alpha-(N3'-histidyl)FAD" EXACT RESID-alternate []
-synonym: "8alpha-N1-histidyl FAD" RELATED RESID-misnomer []
-synonym: "FAD" RELATED PSI-MS-label []
-synonym: "Flavin adenine dinucleotide" RELATED Unimod-description []
-synonym: "MOD_RES Pros-8alpha-FAD histidine" EXACT UniProt-feature []
-synonym: "N(pi)-(8alpha-FAD)-histidine" EXACT RESID-alternate []
-synonym: "Np8aFADHis" EXACT PSI-MOD-label []
-synonym: "pros-(8alpha-FAD)-histidine" EXACT RESID-alternate []
-property_value: DiffAvg "783.54" xsd:float
-property_value: DiffFormula "C 27 H 31 N 9 O 15 P 2" xsd:string
-property_value: DiffMono "783.141485" xsd:float
-property_value: Formula "C 33 H 38 N 12 O 16 P 2" xsd:string
-property_value: MassAvg "920.68" xsd:float
-property_value: MassMono "920.200396" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:50
-xref: uniprot.ptm:PTM-0258
-is_a: MOD:00895
-is_a: MOD:00909
-
-[Term]
-id: MOD:00154
-name: O4'-(8alpha-FAD)-L-tyrosine
-def: "A protein modification that effectively converts an L-tyrosine residue to O4'-(8alpha-FAD)-L-tyrosine." [DeltaMass:0, PubMed:7391034, RESID:AA0145, Unimod:50#Y]
-comment: From DeltaMass: Average Mass: 783
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-(4-[8alpha-riboflavin 5'-(trihydrogen diphosphate) 5'->5'-ester with adenosine]oxyphenyl)propanoic acid" EXACT RESID-systematic []
-synonym: "8alpha-(O4'-tyrosyl)FAD" EXACT RESID-alternate []
-synonym: "FAD" RELATED PSI-MS-label []
-synonym: "Flavin adenine dinucleotide" RELATED Unimod-description []
-synonym: "MOD_RES O-8alpha-FAD tyrosine" EXACT UniProt-feature []
-synonym: "O-8 alpha-Flavin [FAD])- (of Tyrosine)" EXACT DeltaMass-label []
-synonym: "O4'-(8alpha-FAD)-L-tyrosine" EXACT RESID-name []
-synonym: "O8aFADTyr" EXACT PSI-MOD-label []
-property_value: DiffAvg "783.54" xsd:float
-property_value: DiffFormula "C 27 H 31 N 9 O 15 P 2" xsd:string
-property_value: DiffMono "783.141485" xsd:float
-property_value: Formula "C 36 H 40 N 10 O 17 P 2" xsd:string
-property_value: MassAvg "946.72" xsd:float
-property_value: MassMono "946.204813" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:50
-xref: uniprot.ptm:PTM-0231
-is_a: MOD:00895
-is_a: MOD:00919
-
-[Term]
-id: MOD:00155
-name: L-3',4'-dihydroxyphenylalanine
-def: "A protein modification that effectively converts an L-tyrosine residue to L-3',4'-dihydroxyphenylalanine." [DeltaMass:0, OMSSA:194, OMSSA:64, PubMed:1610822, PubMed:1903612, PubMed:3734192, RESID:AA0146, Unimod:35#Y, ChEBI:141815]
-comment: incidental to RESID:AA0368 From DeltaMass: Average Mass: 16
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-(3,4-dihydroxyphenyl)propanoic acid" EXACT RESID-systematic []
-synonym: "3,4-Dihydroxy-Phenylalanine (from Tyrosine) (DOPA)" EXACT DeltaMass-label []
-synonym: "3HyTyr" EXACT PSI-MOD-label []
-synonym: "hydroxylationy" EXACT OMSSA-label []
-synonym: "L-3',4'-dihydroxyphenylalanine" EXACT RESID-name []
-synonym: "L-3'-hydroxytyrosine" EXACT RESID-alternate []
-synonym: "L-DOPA" EXACT RESID-alternate []
-synonym: "levodopa" EXACT RESID-alternate []
-synonym: "mod194" EXACT OMSSA-label []
-synonym: "MOD_RES 3',4'-dihydroxyphenylalanine" EXACT UniProt-feature []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 9 H 9 N 1 O 3" xsd:string
-property_value: MassAvg "179.18" xsd:float
-property_value: MassMono "179.058243" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:35
-xref: uniprot.ptm:PTM-0023
-is_a: MOD:00425
-is_a: MOD:00707
-
-[Term]
-id: MOD:00156
-name: L-2',4',5'-topaquinone
-def: "A protein modification that effectively converts an L-tyrosine residue to an L-2',4',5'-topaquinone." [ChEBI:21187, PubMed:10387067, PubMed:1457410, PubMed:1569055, PubMed:2111581, RESID:AA0147, Unimod:392#Y]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-(5-hydroxy-2,5-cyclohexadien-1,4-dion-2-yl)propanoic acid" EXACT RESID-systematic []
-synonym: "2,4,5-trihydroxyphenylalanine quinone" EXACT RESID-alternate []
-synonym: "5-(2-carboxy-2-aminoethyl)-2-hydroxy-1,4-benzoquinone" EXACT RESID-alternate []
-synonym: "L-2',4',5'-topaquinone" EXACT RESID-name []
-synonym: "L-2,4,5-TOPAquinone" EXACT RESID-alternate []
-synonym: "MOD_RES 2',4',5'-topaquinone" EXACT UniProt-feature []
-synonym: "Quinone" RELATED PSI-MS-label []
-synonym: "quinone" RELATED Unimod-description []
-synonym: "TopaQ" EXACT PSI-MOD-label []
-synonym: "TPQ" EXACT RESID-alternate []
-property_value: DiffAvg "29.98" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 2" xsd:string
-property_value: DiffMono "29.974179" xsd:float
-property_value: Formula "C 9 H 7 N 1 O 4" xsd:string
-property_value: MassAvg "193.16" xsd:float
-property_value: MassMono "193.037508" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:392
-xref: uniprot.ptm:PTM-0009
-is_a: MOD:00679
-is_a: MOD:00919
-
-[Term]
-id: MOD:00157
-name: L-tryptophyl quinone
-def: "A protein modification that effectively converts an L-tryptophan residue to an L-tryptophan quinone." [DeltaMass:0, PubMed:2028257, RESID:AA0148, Unimod:392#W]
-comment: incidental to RESID:AA0149; incidental to RESID:AA0313; From DeltaMass: Average Mass: 30.
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-(6,7-dioxo-1H-indol-3-yl)propanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-3-(6,7-dioxo-6,7-dihydro-1H-indol-3-yl)-propionic acid" EXACT RESID-alternate []
-synonym: "3-[(2S)-2-amino-2-carboxyethyl]-6,7-indolinedione" EXACT RESID-alternate []
-synonym: "6,7 Dione (from Tryptophan)" EXACT DeltaMass-label []
-synonym: "L-tryptophyl quinone" EXACT RESID-name []
-synonym: "MOD_RES Tryptophylquinone" EXACT UniProt-feature []
-synonym: "N-(3-carboxy-1-oxopropyl)-L-tryptophan" EXACT RESID-alternate []
-synonym: "Quinone" RELATED PSI-MS-label []
-synonym: "quinone" RELATED Unimod-description []
-synonym: "TrpQ" EXACT PSI-MOD-label []
-property_value: DiffAvg "29.98" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 2" xsd:string
-property_value: DiffMono "29.974179" xsd:float
-property_value: Formula "C 11 H 8 N 2 O 3" xsd:string
-property_value: MassAvg "216.20" xsd:float
-property_value: MassMono "216.053492" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:392
-xref: uniprot.ptm:PTM-0299
-is_a: MOD:00679
-is_a: MOD:00918
-
-[Term]
-id: MOD:00158
-name: 4'-(L-tryptophan)-L-tryptophyl quinone
-def: "A protein modification that effectively cross-links two L-tryptophan residues by a carbon-carbon bond to form 4'-(L-tryptophan)-L-tryptophyl quinone." [ChEBI:20251, DeltaMass:0, PubMed:2028257, RESID:AA0149]
-comment: Cross-link 2; secondary to RESID:AA0148; From DeltaMass: Average Mass: 28.
-subset: PSI-MOD-slim
-synonym: "2,4-BisTrp-6,7-dione (from Tryptophan)" EXACT DeltaMass-label []
-synonym: "2-amino-3-[2-[2-amino-3-(2-carboxyethyl)-6,7-dioxo-1H-indol-4-yl]-1H-indol-3-yl]propanoic acid" EXACT RESID-alternate []
-synonym: "3-[(2S)-2-amino-2-carboxyethyl]-4-(3-[(2S)-2-amino-2-carboxyethyl]-1H-indol-2-yl)-6,7-indolinedione" EXACT RESID-systematic []
-synonym: "4'-tryptophan-tryptophylquinone" EXACT RESID-alternate []
-synonym: "4-(2'-tryptophyl)tryptophan-6,7-dione" EXACT RESID-alternate []
-synonym: "4-(L-tryptophan-2-yl)-L-tryptophyl quinone" EXACT RESID-name []
-synonym: "alpha,alpha'-diamino-6',7'-dihydro-6',7'-dioxo-(2,4'-bi-1H-indole)-3,3'-dipropanoic acid" EXACT RESID-alternate []
-synonym: "CROSSLNK Tryptophan tryptophylquinone (Trp-Trp)" EXACT UniProt-feature []
-synonym: "TTQ" EXACT RESID-alternate []
-synonym: "XLNK-4'Trp-TrpQ" EXACT PSI-MOD-label []
-property_value: DiffAvg "27.97" xsd:float
-property_value: DiffFormula "C 0 H -4 N 0 O 2" xsd:string
-property_value: DiffMono "27.958529" xsd:float
-property_value: Formula "C 22 H 16 N 4 O 4" xsd:string
-property_value: MassAvg "400.39" xsd:float
-property_value: MassMono "400.117155" xsd:float
-property_value: Origin "W, W" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0298
-is_a: MOD:00692
-is_a: MOD:02057
-
-[Term]
-id: MOD:00159
-name: O-phosphopantetheine-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O-phosphopantetheine-L-serine." [DeltaMass:0, PubMed:10320345, PubMed:10997907, PubMed:12057197, PubMed:12869567, PubMed:4568609, RESID:AA0150, Unimod:49#S]
-comment: Unimod has DiffFormula C 11 H 20 N 2 O 6 P 1 S 1 From DeltaMass: Average Mass: 339
-subset: PSI-MOD-slim
-synonym: "(2R)-2-hydroxy-3,3-dimethyl-4-[(2S)-2-amino-2-carboxyethyl]phosphonato-N-(3-oxo-3-[(2-sulfanylethyl)amino]propyl)butanamide" EXACT RESID-systematic []
-synonym: "4'-Phosphopantetheine" EXACT DeltaMass-label []
-synonym: "MOD_RES O-(pantetheine 4'-phosphoryl)serine" EXACT UniProt-feature []
-synonym: "O-phosphopantetheine-L-serine" EXACT RESID-name []
-synonym: "OPpantSer" EXACT PSI-MOD-label []
-synonym: "Phosphopantetheine" RELATED PSI-MS-label []
-synonym: "Phosphopantetheine" RELATED Unimod-description []
-property_value: DiffAvg "340.33" xsd:float
-property_value: DiffFormula "C 11 H 21 N 2 O 6 P 1 S 1" xsd:string
-property_value: DiffMono "340.085794" xsd:float
-property_value: Formula "C 14 H 26 N 3 O 8 P 1 S 1" xsd:string
-property_value: MassAvg "427.41" xsd:float
-property_value: MassMono "427.117822" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:49
-xref: uniprot.ptm:PTM-0391
-is_a: MOD:00861
-is_a: MOD:00916
-
-[Term]
-id: MOD:00160
-name: N4-glycosyl-L-asparagine
-def: "A protein modification that effectively converts an L-asparagine residue to an N4-glycosyl-L-asparagine." [PubMed:111247, PubMed:1694179, PubMed:5490222, RESID:AA0151#var]
-subset: PSI-MOD-slim
-synonym: "N4GlycoAsn" EXACT PSI-MOD-label []
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00006
-is_a: MOD:00903
-
-[Term]
-id: MOD:00161
-name: S-glucosyl-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-glucosylated L-cysteine." [PubMed:1145128, PubMed:15279557, PubMed:5286858, RESID:AA0152, Unimod:41#C]
-synonym: "(2R)-2-amino-3-[(beta-D-glucopyranosyl)sulfanyl]propanoic acid" EXACT RESID-systematic []
-synonym: "CARBOHYD S-linked (Glc) cysteine" EXACT UniProt-feature []
-synonym: "Hex" RELATED PSI-MS-label []
-synonym: "Hexose" RELATED Unimod-description []
-synonym: "S-(beta-D-glucopyranosyl)cysteine" EXACT RESID-alternate []
-synonym: "S-glucosyl-L-cysteine" EXACT RESID-name []
-synonym: "S-glycosyl-cysteine" EXACT RESID-alternate []
-synonym: "SGlcCys" EXACT PSI-MOD-label []
-property_value: DiffAvg "162.14" xsd:float
-property_value: DiffFormula "C 6 H 10 N 0 O 5 S 0" xsd:string
-property_value: DiffMono "162.052823" xsd:float
-property_value: Formula "C 9 H 15 N 1 O 6 S 1" xsd:string
-property_value: MassAvg "265.28" xsd:float
-property_value: MassMono "265.062008" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:41
-xref: uniprot.ptm:PTM-0626
-is_a: MOD:00426
-is_a: MOD:00433
-is_a: MOD:00905
-
-[Term]
-id: MOD:00162
-name: O5-glucosylgalactosyl-L-hydroxylysine
-def: "A protein modification that effectively converts an L-lysine residue to O5-glucosylgalactosyl-L-hydroxylysine." [PubMed:15149698, PubMed:4288358, PubMed:4319110, RESID:AA0153, Unimod:393]
-comment: Secondary to RESID:AA0028.
-subset: PSI-MOD-slim
-synonym: "(2S,5R)-2,6-diamino-5-[2-O-(alpha-D-glucopyranosyl)-beta-D-galactopyranosyloxy]hexanoic acid" EXACT RESID-systematic []
-synonym: "5-(2-O-alpha-D-glucopyranosyl-beta-D-galactopyranosyl)oxy-L-lysine" EXACT RESID-alternate []
-synonym: "Glucosylgalactosyl" RELATED PSI-MS-label []
-synonym: "glucosylgalactosyl hydroxylysine" RELATED Unimod-description []
-synonym: "O5-glucosylgalactosyl-L-hydroxylysine" EXACT RESID-name []
-synonym: "OGlcGal5HyLys" EXACT PSI-MOD-label []
-property_value: DiffAvg "340.28" xsd:float
-property_value: DiffFormula "C 12 H 20 N 0 O 11" xsd:string
-property_value: DiffMono "340.100561" xsd:float
-property_value: Formula "C 18 H 32 N 2 O 12" xsd:string
-property_value: MassAvg "468.46" xsd:float
-property_value: MassMono "468.195524" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:393
-relationship: derives_from MOD:00037
-is_a: MOD:00912
-is_a: MOD:00396
-
-[Term]
-id: MOD:00163
-name: O-(N-acetylamino)galactosyl-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O-(N-acetylaminogalactosyl)-L-serine." [PubMed:115869, PubMed:16005634, PubMed:3086323, PubMed:8948436, PubMed:9092502, RESID:AA0154]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-(2-acetamido-2-deoxy-alpha-D-galactopyranosyloxy)propanoic acid" EXACT RESID-systematic []
-synonym: "CARBOHYD O-linked (GalNAc) serine" EXACT UniProt-feature []
-synonym: "HexNAc" RELATED PSI-MS-label []
-synonym: "mucin type O-glycosylserine" EXACT RESID-alternate []
-synonym: "O-(N-acetylamino)galactosyl-L-serine" EXACT RESID-name []
-synonym: "O3-(N-acetylgalactosaminyl)serine" EXACT RESID-alternate []
-synonym: "OGalNAcSer" EXACT PSI-MOD-label []
-property_value: DiffAvg "203.19" xsd:float
-property_value: DiffFormula "C 8 H 13 N 1 O 5" xsd:string
-property_value: DiffMono "203.079373" xsd:float
-property_value: Formula "C 11 H 18 N 2 O 7" xsd:string
-property_value: MassAvg "290.27" xsd:float
-property_value: MassMono "290.111401" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0564
-is_a: MOD:00563
-is_a: MOD:01675
-
-[Term]
-id: MOD:00164
-name: O-(N-acetylamino)galactosyl-L-threonine
-def: "A protein modification that effectively converts an L-asparagine residue to O-(N-acetylaminogalactosyl)-L-threonine." [PubMed:16005634, PubMed:1997327, PubMed:3086323, PubMed:8948436, PubMed:9092502, RESID:AA0155]
-subset: PSI-MOD-slim
-synonym: "(2S,3R)-2-amino-3-(2-acetamido-2-deoxy-alpha-D-galactopyranosyloxy)butanoic acid" EXACT RESID-systematic []
-synonym: "CARBOHYD O-linked (GalNAc) threonine" EXACT UniProt-feature []
-synonym: "CARBOHYD O-linked (HexNAc)" EXACT UniProt-feature []
-synonym: "HexNAc" RELATED PSI-MS-label []
-synonym: "mucin type O-glycosylthreonine" EXACT RESID-alternate []
-synonym: "O-(N-acetylamino)galactosyl-L-threonine" EXACT RESID-name []
-synonym: "O3-(N-acetylgalactosaminyl)threonine" EXACT RESID-alternate []
-synonym: "OGalNAcThr" EXACT PSI-MOD-label []
-property_value: DiffAvg "203.19" xsd:float
-property_value: DiffFormula "C 8 H 13 N 1 O 5" xsd:string
-property_value: DiffMono "203.079373" xsd:float
-property_value: Formula "C 12 H 20 N 2 O 7" xsd:string
-property_value: MassAvg "304.30" xsd:float
-property_value: MassMono "304.127051" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0567
-is_a: MOD:00563
-is_a: MOD:01676
-
-[Term]
-id: MOD:00165
-name: 1'-mannosyl-L-tryptophan
-def: "A protein modification that effectively converts an L-tryptophan residue to 1'-mannosyl-L-tryptophan." [PubMed:1482345, PubMed:16150691, RESID:AA0156]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-(1-D-mannopyranosyloxy-1H-indol-3-yl)propanoic acid" EXACT RESID-systematic []
-synonym: "1'-glycosyl-L-tryptophan" EXACT RESID-alternate []
-synonym: "1'-mannosyl-L-tryptophan" EXACT RESID-name []
-synonym: "CARBOHYD N-linked (Man) tryptophan" EXACT UniProt-feature []
-synonym: "N-mannosyl-tryptophan" EXACT RESID-alternate []
-synonym: "N1'ManTrp" EXACT PSI-MOD-label []
-synonym: "N1-mannosyl-tryptophan" EXACT RESID-alternate []
-property_value: DiffAvg "162.14" xsd:float
-property_value: DiffFormula "C 6 H 10 N 0 O 5" xsd:string
-property_value: DiffMono "162.052823" xsd:float
-property_value: Formula "C 17 H 20 N 2 O 6" xsd:string
-property_value: MassAvg "348.36" xsd:float
-property_value: MassMono "348.132136" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0535
-is_a: MOD:00006
-is_a: MOD:00595
-is_a: MOD:00918
-
-[Term]
-id: MOD:00166
-name: O4'-glucosyl-L-tyrosine
-def: "A protein modification that effectively converts an L-tyrosine residue to O4'-glucosyl-tyrosine." [PubMed:15279557, PubMed:3181138, RESID:AA0157, Unimod:41#Y]
-synonym: "(2S)-2-amino-3-(4-alpha-D-glucopyranosyloxy)phenylpropanoic acid" EXACT RESID-systematic []
-synonym: "Hex" RELATED PSI-MS-label []
-synonym: "Hexose" RELATED Unimod-description []
-synonym: "O4'-glucosyl-L-tyrosine" EXACT RESID-name []
-synonym: "O4'-glycosyl-L-tyrosine" EXACT RESID-alternate []
-synonym: "O4GlcTyr" EXACT PSI-MOD-label []
-synonym: "CARBOHYD O-linked (Glc) tyrosine" EXACT UniProt-feature []
-property_value: DiffAvg "162.14" xsd:float
-property_value: DiffFormula "C 6 H 10 N 0 O 5" xsd:string
-property_value: DiffMono "162.052823" xsd:float
-property_value: Formula "C 15 H 19 N 1 O 7" xsd:string
-property_value: MassAvg "325.32" xsd:float
-property_value: MassMono "325.116152" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:41
-xref: uniprot.ptm:PTM-0575
-is_a: MOD:00433
-is_a: MOD:01927
-
-[Term]
-id: MOD:00167
-name: N-asparaginyl-glycosylphosphatidylinositolethanolamine
-def: "A protein modification that effectively converts an L-asparagine residue to N-asparaginyl-glycosylphosphatidylinositolethanolamine." [PubMed:1824714, PubMed:8276756, RESID:AA0158]
-synonym: "GPIAsn" EXACT PSI-MOD-label []
-synonym: "LIPID GPI-anchor amidated asparagine" EXACT UniProt-feature []
-synonym: "N-asparaginyl-glycosylphosphatidylinositolethanolamine" EXACT RESID-name []
-property_value: DiffAvg "123.05" xsd:float
-property_value: DiffFormula "C 2 H 6 N 1 O 3 P 1" xsd:string
-property_value: DiffMono "123.008530" xsd:float
-property_value: Formula "C 6 H 13 N 3 O 6 P 1" xsd:string
-property_value: MassAvg "254.16" xsd:float
-property_value: MassMono "254.054197" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0137
-is_a: MOD:00818
-is_a: MOD:00903
-
-[Term]
-id: MOD:00168
-name: N-aspartyl-glycosylphosphatidylinositolethanolamine
-def: "A protein modification that effectively converts an L-aspartic acid residue to N-(aspart-1-yl)-glycosylphosphatidylinositolethanolamine." [PubMed:7120400, RESID:AA0159]
-synonym: "GPIAsp" EXACT PSI-MOD-label []
-synonym: "LIPID GPI-anchor amidated aspartate" EXACT UniProt-feature []
-synonym: "N-aspartyl-glycosylphosphatidylinositolethanolamine" EXACT RESID-name []
-property_value: DiffAvg "123.05" xsd:float
-property_value: DiffFormula "C 2 H 6 N 1 O 3 P 1" xsd:string
-property_value: DiffMono "123.008530" xsd:float
-property_value: Formula "C 6 H 12 N 2 O 7 P 1" xsd:string
-property_value: MassAvg "255.14" xsd:float
-property_value: MassMono "255.038212" xsd:float
-property_value: Origin "D" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0138
-is_a: MOD:00818
-is_a: MOD:00904
-
-[Term]
-id: MOD:00169
-name: N-cysteinyl-glycosylphosphatidylinositolethanolamine
-def: "A protein modification that effectively converts an L-cysteine residue to N-cysteinyl-glycosylphosphatidylinositolethanolamine." [PubMed:2897081, RESID:AA0160]
-synonym: "GPICys" EXACT PSI-MOD-label []
-synonym: "LIPID GPI-anchor amidated cysteine" EXACT UniProt-feature []
-synonym: "N-cysteinyl-glycosylphosphatidylinositolethanolamine" EXACT RESID-name []
-property_value: DiffAvg "123.05" xsd:float
-property_value: DiffFormula "C 2 H 6 N 1 O 3 P 1 S 0" xsd:string
-property_value: DiffMono "123.008530" xsd:float
-property_value: Formula "C 5 H 12 N 2 O 5 P 1 S 1" xsd:string
-property_value: MassAvg "243.19" xsd:float
-property_value: MassMono "243.020454" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0140
-is_a: MOD:00818
-is_a: MOD:00905
-
-[Term]
-id: MOD:00170
-name: N-glycyl-glycosylphosphatidylinositolethanolamine
-def: "A protein modification that effectively converts a glycine residue to N-glycyl-glycosylphosphatidylinositolethanolamine." [PubMed:2341397, RESID:AA0161]
-synonym: "GPIGly" EXACT PSI-MOD-label []
-synonym: "LIPID GPI-anchor amidated glycine" EXACT UniProt-feature []
-synonym: "N-glycyl-glycosylphosphatidylinositolethanolamine" EXACT RESID-name []
-property_value: DiffAvg "123.05" xsd:float
-property_value: DiffFormula "C 2 H 6 N 1 O 3 P 1" xsd:string
-property_value: DiffMono "123.008530" xsd:float
-property_value: Formula "C 4 H 10 N 2 O 5 P 1" xsd:string
-property_value: MassAvg "197.11" xsd:float
-property_value: MassMono "197.032733" xsd:float
-property_value: Origin "G" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0141
-is_a: MOD:00818
-is_a: MOD:00908
-
-[Term]
-id: MOD:00171
-name: N-seryl-glycosylphosphatidylinositolethanolamine
-def: "A protein modification that effectively converts an L-serine residue to N-seryl-glycosylphosphatidylinositolethanolamine." [PubMed:2111324, PubMed:8448158, RESID:AA0162]
-synonym: "GPISer" EXACT PSI-MOD-label []
-synonym: "LIPID GPI-anchor amidated serine" EXACT UniProt-feature []
-synonym: "N-seryl-glycosylphosphatidylinositolethanolamine" EXACT RESID-name []
-property_value: DiffAvg "123.05" xsd:float
-property_value: DiffFormula "C 2 H 6 N 1 O 3 P 1" xsd:string
-property_value: DiffMono "123.008530" xsd:float
-property_value: Formula "C 5 H 12 N 2 O 6 P 1" xsd:string
-property_value: MassAvg "227.13" xsd:float
-property_value: MassMono "227.043298" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0142
-is_a: MOD:00818
-is_a: MOD:00916
-
-[Term]
-id: MOD:00172
-name: N-alanyl-glycosylphosphatidylinositolethanolamine
-def: "A protein modification that effectively converts an L-alanine residue to N-alanyl-glycosylphosphatidylinositolethanolamine." [PubMed:7682556, PubMed:7744038, RESID:AA0163]
-synonym: "GPIAla" EXACT PSI-MOD-label []
-synonym: "LIPID GPI-anchor amidated alanine" EXACT UniProt-feature []
-synonym: "N-alanyl-glycosylphosphatidylinositolethanolamine" EXACT RESID-name []
-property_value: DiffAvg "123.05" xsd:float
-property_value: DiffFormula "C 2 H 6 N 1 O 3 P 1" xsd:string
-property_value: DiffMono "123.008530" xsd:float
-property_value: Formula "C 5 H 12 N 2 O 5 P 1" xsd:string
-property_value: MassAvg "211.13" xsd:float
-property_value: MassMono "211.048383" xsd:float
-property_value: Origin "A" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0136
-is_a: MOD:00818
-is_a: MOD:00901
-
-[Term]
-id: MOD:00173
-name: N-threonyl-glycosylphosphatidylinositolethanolamine
-def: "A protein modification that effectively converts an L-threonine residue to N-threonyl-glycosylphosphatidylinositolethanolamine." [RESID:AA0164]
-synonym: "GPIThr" EXACT PSI-MOD-label []
-synonym: "LIPID GPI-anchor amidated threonine" EXACT UniProt-feature []
-synonym: "N-threonyl-glycosylphosphatidylinositolethanolamine" EXACT RESID-name []
-property_value: DiffAvg "123.05" xsd:float
-property_value: DiffFormula "C 2 H 6 N 1 O 3 P 1" xsd:string
-property_value: DiffMono "123.008530" xsd:float
-property_value: Formula "C 6 H 14 N 2 O 6 P 1" xsd:string
-property_value: MassAvg "241.16" xsd:float
-property_value: MassMono "241.058948" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "hypothetical" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0143
-is_a: MOD:00818
-is_a: MOD:00917
-
-[Term]
-id: MOD:00174
-name: N-glycyl-glycosylsphingolipidinositolethanolamine
-def: "A protein modification that effectively converts a glycine residue to N-glycyl-glycosylsphingolipidinositolethanolamine." [PubMed:12626404, PubMed:8404891, RESID:AA0165]
-synonym: "GSIGly" EXACT PSI-MOD-label []
-synonym: "LIPID GPI-like-anchor amidated glycine" EXACT UniProt-feature []
-synonym: "N-glycyl-glycosylsphingolipidinositolethanolamine" EXACT RESID-name []
-property_value: DiffAvg "123.05" xsd:float
-property_value: DiffFormula "C 2 H 6 N 1 O 3 P 1" xsd:string
-property_value: DiffMono "123.008530" xsd:float
-property_value: Formula "C 4 H 10 N 2 O 5 P 1" xsd:string
-property_value: MassAvg "197.11" xsd:float
-property_value: MassMono "197.032733" xsd:float
-property_value: Origin "G" xsd:string
-property_value: Source "hypothetical" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0146
-is_a: MOD:00466
-is_a: MOD:00908
-
-[Term]
-id: MOD:00175
-name: N-seryl-glycosylsphingolipidinositolethanolamine
-def: "A protein modification that effectively converts an L-serine residue to N-seryl-glycosylsphingolipidinositolethanolamine." [PubMed:12626404, PubMed:2721485, PubMed:8269952, RESID:AA0166]
-synonym: "GSISer" EXACT PSI-MOD-label []
-synonym: "LIPID GPI-like-anchor amidated serine" EXACT UniProt-feature []
-synonym: "N-seryl-glycosylsphingolipidinositolethanolamine" EXACT RESID-name []
-property_value: DiffAvg "123.05" xsd:float
-property_value: DiffFormula "C 2 H 6 N 1 O 3 P 1" xsd:string
-property_value: DiffMono "123.008530" xsd:float
-property_value: Formula "C 5 H 12 N 2 O 6 P 1" xsd:string
-property_value: MassAvg "227.13" xsd:float
-property_value: MassMono "227.043298" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0147
-is_a: MOD:00466
-is_a: MOD:00916
-
-[Term]
-id: MOD:00176
-name: O-(phosphoribosyl dephospho-coenzyme A)-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O-(phosphoribosyl dephospho-coenzyme A)-L-serine." [PubMed:10924139, PubMed:11052675, PubMed:179809, PubMed:180526, PubMed:368065, RESID:AA0167, Unimod:395#S]
-comment: pRibodePcoA
-subset: PSI-MOD-slim
-synonym: "MOD_RES O-(phosphoribosyl dephospho-coenzyme A)serine" EXACT UniProt-feature []
-synonym: "O-(phosphoribosyl dephospho-coenzyme A)-L-serine" EXACT RESID-name []
-synonym: "O3-(phosphate-5-ribosyl-alpha-2-adenosine-5-diphosphate pantetheine)-L-serine" EXACT RESID-alternate []
-synonym: "O3-(phosphoribosyl dephospho-coenzyme A)-L-serine" EXACT RESID-alternate []
-synonym: "O3-2'-(5''-phosphoribosyl-3'-dephosphocoenzyme A)-L-serine" EXACT RESID-alternate []
-synonym: "OPRibdPCoASer" EXACT PSI-MOD-label []
-synonym: "phosphoribosyl dephospho-coenzyme A" RELATED Unimod-description []
-synonym: "PhosphoribosyldephosphoCoA" RELATED PSI-MS-label []
-property_value: DiffAvg "881.63" xsd:float
-property_value: DiffFormula "C 26 H 42 N 7 O 19 P 3 S 1" xsd:string
-property_value: DiffMono "881.146903" xsd:float
-property_value: Formula "C 29 H 47 N 8 O 21 P 3 S 1" xsd:string
-property_value: MassAvg "968.71" xsd:float
-property_value: MassMono "968.178931" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:395
-xref: uniprot.ptm:PTM-0389
-is_a: MOD:00860
-is_a: MOD:00861
-is_a: MOD:00916
-
-[Term]
-id: MOD:00177
-name: omega-N-(ADP-ribosyl)-L-arginine
-def: "A protein modification that effectively converts an L-argininine residue to omega-N-(ADP-ribosyl)-L-arginine." [DeltaMass:0, PubMed:15842200, PubMed:209022, PubMed:3090031, PubMed:3923473, PubMed:6582062, RESID:AA0168, Unimod:213#R]
-comment: From DeltaMass: Average Mass: 541.
-subset: PSI-MOD-slim
-synonym: "(S)-2-amino-5-([imino([adenosine 5'-(trihydrogen diphosphate) 5'->5'-ester with alpha-D-ribofuranosyl]amino)methyl]amino)pentanoic acid" EXACT RESID-systematic []
-synonym: "ADP Ribose addition" RELATED Unimod-description []
-synonym: "ADP-Ribosyl" RELATED PSI-MS-label []
-synonym: "ADPRibArg" EXACT PSI-MOD-label []
-synonym: "MOD_RES ADP-ribosylarginine" EXACT UniProt-feature []
-synonym: "N(omega)-[alpha-D-ribofuranoside 5'->5'-ester with adenosine 5'-(trihydrogen diphosphate)]-L-arginine" EXACT RESID-alternate []
-synonym: "N(omega)-alpha-D-ribofuranosyl-L-arginine 5'->5'-ester with adenosine 5'-(trihydrogen diphosphate)" EXACT RESID-alternate []
-synonym: "N-(ADP-ribosyl)- (on Arginine)" EXACT DeltaMass-label []
-synonym: "omega-N-(ADP-ribosyl)-L-arginine" EXACT RESID-name []
-property_value: DiffAvg "541.30" xsd:float
-property_value: DiffFormula "C 15 H 21 N 5 O 13 P 2" xsd:string
-property_value: DiffMono "541.061109" xsd:float
-property_value: Formula "C 21 H 33 N 9 O 14 P 2" xsd:string
-property_value: MassAvg "697.49" xsd:float
-property_value: MassMono "697.162220" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:213
-xref: uniprot.ptm:PTM-0053
-is_a: MOD:00752
-is_a: MOD:00902
-
-[Term]
-id: MOD:00178
-name: S-(ADP-ribosyl)-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-(ADP-ribosyl)-L-cysteine." [DeltaMass:0, PubMed:15842200, PubMed:3863818, RESID:AA0169, Unimod:213#C]
-comment: From DeltaMass: Average Mass: 541.
-subset: PSI-MOD-slim
-synonym: "(R)-2-amino-3-([adenosine 5'-(trihydrogen diphosphate) 5'->5'-ester with alpha-D-ribofuranosyl]sulfanyl)propanoic acid" EXACT RESID-systematic []
-synonym: "ADP Ribose addition" RELATED Unimod-description []
-synonym: "ADP-Ribosyl" RELATED PSI-MS-label []
-synonym: "ADPRibCys" EXACT PSI-MOD-label []
-synonym: "MOD_RES ADP-ribosylcysteine" EXACT UniProt-feature []
-synonym: "S-(ADP-ribosyl)- (on Cysteine)" EXACT DeltaMass-label []
-synonym: "S-(ADP-ribosyl)-L-cysteine" EXACT RESID-name []
-synonym: "S-alpha-D-ribofuranosyl-L-cysteine 5'->5'-ester with adenosine 5'-(trihydrogen diphosphate)" EXACT RESID-alternate []
-synonym: "S-L-cysteine alpha-D-ribofuranoside 5'->5'-ester with adenosine 5'-(trihydrogen diphosphate)" EXACT RESID-alternate []
-property_value: DiffAvg "541.30" xsd:float
-property_value: DiffFormula "C 15 H 21 N 5 O 13 P 2 S 0" xsd:string
-property_value: DiffMono "541.061109" xsd:float
-property_value: Formula "C 18 H 26 N 6 O 14 P 2 S 1" xsd:string
-property_value: MassAvg "644.44" xsd:float
-property_value: MassMono "644.070294" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:213
-xref: uniprot.ptm:PTM-0055
-is_a: MOD:00752
-is_a: MOD:00905
-
-[Term]
-id: MOD:00179
-name: L-glutamyl 5-glycerylphosphorylethanolamine
-def: "A protein modification that effectively converts an L-glutamic acid residue to L-glutamyl 5-glycerylphosphorylethanolamine." [PubMed:2511205, PubMed:2569467, PubMed:9662537, RESID:AA0170, Unimod:396#E]
-comment: glycerylPE
-subset: PSI-MOD-slim
-synonym: "(S)-2-amino-5-[2-([([2,3-dihydroxypropyl]oxy)(hydroxy)phosphoryl]oxy)ethyl]amino-5-oxopentanoic acid" EXACT RESID-systematic []
-synonym: "5-L-glutamyl glycerylphosphorylethanolamine" EXACT RESID-name []
-synonym: "5GlyceroPEtAGlu" EXACT PSI-MOD-label []
-synonym: "GlycerylPE" RELATED PSI-MS-label []
-synonym: "glycerylphosphorylethanolamine" RELATED Unimod-description []
-synonym: "L-glutamyl 5-glycerophosphoethanolamine" EXACT RESID-alternate []
-synonym: "L-glutamyl 5-glycerophosphorylethanolamine" EXACT RESID-alternate []
-synonym: "L-glutamyl 5-glycerylphosphorylethanolamine" EXACT RESID-alternate []
-synonym: "MOD_RES 5-glutamyl glycerylphosphorylethanolamine" EXACT UniProt-feature []
-property_value: DiffAvg "197.13" xsd:float
-property_value: DiffFormula "C 5 H 12 N 1 O 5 P 1" xsd:string
-property_value: DiffMono "197.045309" xsd:float
-property_value: Formula "C 10 H 19 N 2 O 8 P 1" xsd:string
-property_value: MassAvg "326.24" xsd:float
-property_value: MassMono "326.087902" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:396
-xref: uniprot.ptm:PTM-0403
-is_a: MOD:00906
-
-[Term]
-id: MOD:00180
-name: S-sulfo-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-sulfo-L-cysteine." [PubMed:12876326, PubMed:14752058, PubMed:643076, RESID:AA0171, Unimod:40#C]
-synonym: "(2R)-2-amino-3-(sulfosulfanyl)propanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-3-(sulfothio)propanoic acid" EXACT RESID-alternate []
-synonym: "3-(sulfosulfanyl)-L-alanine" EXACT RESID-alternate []
-synonym: "cysteine sulfate thioester" EXACT RESID-alternate []
-synonym: "cysteine-S-sulfonic acid" EXACT RESID-alternate []
-synonym: "O-Sulfonation" RELATED Unimod-description []
-synonym: "S-sulfo-L-cysteine" EXACT RESID-name []
-synonym: "S-sulfocysteine" EXACT PSI-MOD-alternate []
-synonym: "S-sulfocysteine" EXACT RESID-alternate []
-synonym: "SSulfCys" EXACT PSI-MOD-label []
-synonym: "Sulfo" RELATED PSI-MS-label []
-property_value: DiffAvg "80.06" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 3 S 1" xsd:string
-property_value: DiffMono "79.956815" xsd:float
-property_value: Formula "C 3 H 5 N 1 O 4 S 2" xsd:string
-property_value: MassAvg "183.20" xsd:float
-property_value: MassMono "182.966000" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:40
-is_a: MOD:00695
-is_a: MOD:00777
-is_a: MOD:00905
-
-[Term]
-id: MOD:00181
-name: O4'-sulfo-L-tyrosine
-def: "A protein modification that effectively converts an L-tyrosine residue to O4'-sulfo-L-tyrosine." [DeltaMass:88, OMSSA:114, PubMed:10226369, PubMed:14752058, PubMed:2303439, PubMed:3778455, PubMed:3801003, RESID:AA0172, Unimod:40#Y]
-comment: From DeltaMass: Average Mass: 80 Average Mass Change:80 PubMed:9624161.
-subset: PSI-MOD-slim
-synonym: "(S)-2-amino-3-(4-sulfooxyphenyl)propanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-3-(4-hydroxyphenyl)propanoic acid 4'-sulfate" EXACT RESID-alternate []
-synonym: "MOD_RES Sulfotyrosine" EXACT UniProt-feature []
-synonym: "O-Sulfonation" RELATED Unimod-description []
-synonym: "O4'-sulfo-L-tyrosine" EXACT RESID-name []
-synonym: "O4-sulfotyrosine" EXACT RESID-alternate []
-synonym: "OSulfTyr" EXACT PSI-MOD-label []
-synonym: "sulfationy" EXACT OMSSA-label []
-synonym: "Sulfo" RELATED PSI-MS-label []
-synonym: "Sulphation (of O of Tyrosine)" EXACT DeltaMass-label []
-synonym: "tyrosine sulfate" EXACT RESID-alternate []
-synonym: "tyrosine-O-sulfonic acid" EXACT RESID-alternate []
-synonym: "tyrosine-O-sulphonic acid" EXACT RESID-alternate []
-synonym: "Tyrosinyl Sulphate" EXACT DeltaMass-label []
-property_value: DiffAvg "80.06" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 3 S 1" xsd:string
-property_value: DiffMono "79.956815" xsd:float
-property_value: Formula "C 9 H 9 N 1 O 5 S 1" xsd:string
-property_value: MassAvg "243.23" xsd:float
-property_value: MassMono "243.020143" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:40
-xref: uniprot.ptm:PTM-0286
-is_a: MOD:00695
-is_a: MOD:00774
-is_a: MOD:00919
-
-[Term]
-id: MOD:00182
-name: L-bromohistidine
-def: "A protein modification that effectively converts an L-histidine residue to L-bromohistidine." [PubMed:2076468, PubMed:9033387, RESID:AA0173, Unimod:340#H]
-synonym: "Br1His" EXACT PSI-MOD-label []
-synonym: "bromination" RELATED Unimod-description []
-synonym: "Bromo" RELATED PSI-MS-label []
-synonym: "L-bromohistidine" EXACT RESID-name []
-synonym: "MOD_RES Bromohistidine" EXACT UniProt-feature []
-property_value: DiffAvg "78.90" xsd:float
-property_value: DiffFormula "Br 1 C 0 H -1 N 0 O 0" xsd:string
-property_value: DiffMono "77.910512" xsd:float
-property_value: Formula "Br 1 C 6 H 6 N 3 O 1" xsd:string
-property_value: MassAvg "216.04" xsd:float
-property_value: MassMono "214.969424" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:340
-xref: uniprot.ptm:PTM-0089
-is_a: MOD:01049
-is_a: MOD:01912
-
-[Term]
-id: MOD:00183
-name: L-2'-bromophenylalanine
-def: "A protein modification that effectively converts an L-phenylalanine residue to L-2'-bromophenylalanine." [DeltaMass:83, PubMed:2059627, PubMed:2076468, PubMed:9033387, RESID:AA0174]
-comment: From DeltaMass: Average Mass: 78 Average Mass Change:78 References:Yoshino,K et.al. Biochemistry Vol. 30 pg 6203-9 (1991) Identifidation of a novel amino acid, o-bromo-L-phenylananine, in egg-associated peptides that activate spermatozoa.
-synonym: "(S)-2-amino-3-(2-bromophenyl)propanoic acid" EXACT RESID-systematic []
-synonym: "2'BrPhe" EXACT PSI-MOD-label []
-synonym: "bromination" RELATED Unimod-description []
-synonym: "Bromo" RELATED PSI-MS-label []
-synonym: "L-2'-bromophenylalanine" EXACT RESID-name []
-synonym: "L-o-bromination of Phe with 79Br" EXACT DeltaMass-label []
-synonym: "o-bromophenylalanine" EXACT RESID-alternate []
-synonym: "ortho-bromophenylalanine" EXACT RESID-alternate []
-property_value: DiffAvg "78.90" xsd:float
-property_value: DiffFormula "Br 1 C 0 H -1 N 0 O 0" xsd:string
-property_value: DiffMono "77.910512" xsd:float
-property_value: Formula "Br 1 C 9 H 8 N 1 O 1" xsd:string
-property_value: MassAvg "226.07" xsd:float
-property_value: MassMono "224.978926" xsd:float
-property_value: Origin "F" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00972
-
-[Term]
-id: MOD:00184
-name: L-3'-bromophenylalanine
-def: "A protein modification that effectively converts an L-phenylalanine residue to L-3'-bromophenylalanine." [PubMed:2076468, PubMed:9033387, RESID:AA0175]
-synonym: "(S)-2-amino-3-(3-bromophenyl)propanoic acid" EXACT RESID-systematic []
-synonym: "3'BrPhe" EXACT PSI-MOD-label []
-synonym: "bromination" RELATED Unimod-description []
-synonym: "Bromo" RELATED PSI-MS-label []
-synonym: "L-3'-bromophenylalanine" EXACT RESID-name []
-synonym: "m-bromophenylalanine" EXACT RESID-alternate []
-synonym: "meta-bromophenylalanine" EXACT RESID-alternate []
-property_value: DiffAvg "78.90" xsd:float
-property_value: DiffFormula "Br 1 C 0 H -1 N 0 O 0" xsd:string
-property_value: DiffMono "77.910512" xsd:float
-property_value: Formula "Br 1 C 9 H 8 N 1 O 1" xsd:string
-property_value: MassAvg "226.07" xsd:float
-property_value: MassMono "224.978926" xsd:float
-property_value: Origin "F" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00972
-
-[Term]
-id: MOD:00185
-name: L-4'-bromophenylalanine
-def: "A protein modification that effectively converts an L-phenylalanine residue to L-4'-bromophenylalanine." [PubMed:2076468, PubMed:9033387, RESID:AA0176]
-synonym: "(2S)-2-amino-3-(4-bromophenyl)propanoic acid" EXACT RESID-systematic []
-synonym: "4'BrPhe" EXACT PSI-MOD-label []
-synonym: "bromination" RELATED Unimod-description []
-synonym: "Bromo" RELATED PSI-MS-label []
-synonym: "L-4'-bromophenylalanine" EXACT RESID-name []
-synonym: "p-bromophenylalanine" EXACT RESID-alternate []
-synonym: "para-bromophenylalanine" EXACT RESID-alternate []
-property_value: DiffAvg "78.90" xsd:float
-property_value: DiffFormula "Br 1 C 0 H -1 N 0 O 0" xsd:string
-property_value: DiffMono "77.910512" xsd:float
-property_value: Formula "Br 1 C 9 H 8 N 1 O 1" xsd:string
-property_value: MassAvg "226.07" xsd:float
-property_value: MassMono "224.978926" xsd:float
-property_value: Origin "F" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00972
-
-[Term]
-id: MOD:00186
-name: 3,3',5-triiodo-L-thyronine
-def: "A protein modification that effectively substitutes an L-tyrosine residue with 3,3',5-triiodo-L-thyronine." [ChEBI:18258, DeltaMass:0, RESID:AA0177, Unimod:397]
-comment: From DeltaMass: Average Mass: 470.
-subset: PSI-MOD-slim
-synonym: "(S)-2-amino-3-[4-(4-hydroxy-3-iodophenoxy)-3,5-diiodophenyl]propanoic acid" EXACT RESID-systematic []
-synonym: "3',3'',5'-triiodo-L-thyronine" EXACT RESID-name []
-synonym: "3,3',5-triiodo-L-thyronine" EXACT RESID-alternate []
-synonym: "3,5,3'-triiodo-L-thyronine" EXACT RESID-alternate []
-synonym: "3,5,3'-Triiodothyronine (from Tyrosine)" EXACT DeltaMass-label []
-synonym: "4-(4-hydroxy-3-iodophenoxy)-3,5-diiodo-L-phenylalanine" EXACT RESID-alternate []
-synonym: "I3Thy" EXACT PSI-MOD-label []
-synonym: "liothyronine" EXACT RESID-alternate []
-synonym: "MOD_RES Triiodothyronine" EXACT UniProt-feature []
-synonym: "O-(4-hydroxy-3-iodophenyl)-3,5-diiodo-L-tyrosine" EXACT RESID-alternate []
-synonym: "T3" EXACT RESID-alternate []
-synonym: "triiodo" RELATED Unimod-description []
-synonym: "Triiodothyronine" RELATED PSI-MS-label []
-property_value: DiffAvg "469.79" xsd:float
-property_value: DiffFormula "C 6 H 1 I 3 N 0 O 1" xsd:string
-property_value: DiffMono "469.716158" xsd:float
-property_value: Formula "C 15 H 10 I 3 N 1 O 3" xsd:string
-property_value: MassAvg "632.96" xsd:float
-property_value: MassMono "632.779486" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:397
-xref: uniprot.ptm:PTM-0295
-is_a: MOD:00998
-
-[Term]
-id: MOD:00187
-name: L-thyroxine
-def: "A protein modification that effectively substitutes an L-tyrosine residue with L-thyroxine." [ChEBI:18332, PubMed:6704086, RESID:AA0178, Unimod:398]
-subset: PSI-MOD-slim
-synonym: "(S)-2-amino-3-[4-(4-hydroxy-3,5-diiodophenoxy)-3,5-diiodophenyl]propanoic acid" EXACT RESID-systematic []
-synonym: "3',3'',5',5''-tetraiodo-L-thyronine" EXACT RESID-alternate []
-synonym: "3,3',5,5'-tetraiodo-L-thyronine" EXACT RESID-alternate []
-synonym: "3,5,3',5'-tetraiodo-L-thyronine" EXACT RESID-alternate []
-synonym: "4-(4-hydroxy-3,5-diiodophenoxy)-3,5-diiodo-L-phenylalanine" EXACT RESID-alternate []
-synonym: "I4Thy" EXACT PSI-MOD-label []
-synonym: "L-thyroxine" EXACT RESID-name []
-synonym: "MOD_RES Thyroxine" EXACT UniProt-feature []
-synonym: "O-(4-hydroxy-3,5-diiodophenyl)-3,5-diiodo-L-tyrosine" EXACT RESID-alternate []
-synonym: "T4" EXACT RESID-alternate []
-synonym: "tetraiodo" RELATED Unimod-description []
-synonym: "Thyroxine" RELATED PSI-MS-label []
-property_value: DiffAvg "595.68" xsd:float
-property_value: DiffFormula "C 6 H 0 I 4 N 0 O 1" xsd:string
-property_value: DiffMono "595.612805" xsd:float
-property_value: Formula "C 15 H 9 I 4 N 1 O 3" xsd:string
-property_value: MassAvg "758.86" xsd:float
-property_value: MassMono "758.676134" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:398
-xref: uniprot.ptm:PTM-0294
-is_a: MOD:00998
-
-[Term]
-id: MOD:00188
-name: 6'-bromo-L-tryptophan
-def: "A protein modification that effectively converts an L-tryptophan residue to 6'-bromo-L-tryptophan." [PubMed:12118011, PubMed:9030520, PubMed:9033387, PubMed:9434739, RESID:AA0179, Unimod:340#W]
-synonym: "(2S)-2-amino-3-(6-bromo-1H-indol-3-yl)propanoic acid" EXACT RESID-systematic []
-synonym: "6'-bromo-L-tryptophan" EXACT RESID-name []
-synonym: "6'-BrTrp" EXACT PSI-MOD-label []
-synonym: "bromination" RELATED Unimod-description []
-synonym: "Bromo" RELATED PSI-MS-label []
-synonym: "MOD_RES 6'-bromotryptophan" EXACT UniProt-feature []
-property_value: DiffAvg "78.90" xsd:float
-property_value: DiffFormula "Br 1 C 0 H -1 N 0 O 0" xsd:string
-property_value: DiffMono "77.910512" xsd:float
-property_value: Formula "Br 1 C 11 H 9 N 2 O 1" xsd:string
-property_value: MassAvg "265.11" xsd:float
-property_value: MassMono "263.989825" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:398
-xref: uniprot.ptm:PTM-0051
-is_a: MOD:01068
-is_a: MOD:01912
-
-[Term]
-id: MOD:00189
-name: dehydroalanine (Ser)
-def: "A protein modification that effectively converts an L-serine residue to dehydroalanine." [DeltaMass:0, OMSSA:140, OMSSA:164, OMSSA:96, PubMed:10220322, PubMed:1547888, PubMed:1815586, PubMed:2914619, PubMed:7947813, PubMed:8239649, RESID:AA0181#SER, Unimod:23#S]
-subset: PSI-MOD-slim
-synonym: "2,3-didehydroalanine" EXACT RESID-alternate []
-synonym: "2-aminoacrylic acid" EXACT RESID-alternate []
-synonym: "2-aminopropenoic acid" EXACT RESID-systematic []
-synonym: "4-methylidene-imidazole-5-one (MIO) active site" EXACT RESID-alternate []
-synonym: "anhydroserine" EXACT RESID-alternate []
-synonym: "beta-elim-s" EXACT OMSSA-label []
-synonym: "Dehydrated" RELATED PSI-MS-label []
-synonym: "dehydro" EXACT OMSSA-label []
-synonym: "dehydroalanine" EXACT RESID-name []
-synonym: "Dha" EXACT RESID-alternate []
-synonym: "Dha(Ser)" EXACT PSI-MOD-label []
-synonym: "MOD_RES 2,3-didehydroalanine (Ser)" EXACT UniProt-feature []
-synonym: "phospholosss" EXACT OMSSA-label []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 3 H 3 N 1 O 1" xsd:string
-property_value: MassAvg "69.06" xsd:float
-property_value: MassMono "69.021464" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:23
-xref: uniprot.ptm:PTM-0006
-is_a: MOD:00416
-is_a: MOD:00916
-is_a: MOD:01168
-
-[Term]
-id: MOD:00190
-name: dehydrobutyrine (Thr)
-def: "A protein modification that effectively converts an L-threonine residue to dehydrobutyrine." [DeltaMass:0, OMSSA:141, OMSSA:164, OMSSA:97, PubMed:1547888, PubMed:3769923, RESID:AA0182, Unimod:23#T]
-subset: PSI-MOD-slim
-synonym: "(2Z)-2-aminobut-2-enoic acid" EXACT RESID-systematic []
-synonym: "(Z)-2-amino-2-butenoic acid" EXACT RESID-alternate []
-synonym: "(Z)-2-aminobutenoic acid" EXACT RESID-alternate []
-synonym: "(Z)-dehydrobutyrine" EXACT RESID-name []
-synonym: "2,3-didehydrobutyrine" EXACT RESID-alternate []
-synonym: "3-methyldehydroalanine" EXACT RESID-alternate []
-synonym: "alpha,beta-dehydroaminobutyric acid" EXACT RESID-alternate []
-synonym: "anhydrothreonine" EXACT RESID-alternate []
-synonym: "beta-elim-t" EXACT OMSSA-label []
-synonym: "Dehydrated" RELATED PSI-MS-label []
-synonym: "Dehydrated" RELATED Unimod-interim []
-synonym: "Dehydration" RELATED Unimod-description []
-synonym: "dehydro" EXACT OMSSA-label []
-synonym: "Dehydroamino butyric acid" EXACT DeltaMass-label []
-synonym: "Dhb" EXACT RESID-alternate []
-synonym: "Dhb(Thr)" EXACT PSI-MOD-label []
-synonym: "methyl-dehydroalanine" EXACT RESID-alternate []
-synonym: "MOD_RES (Z)-2,3-didehydrobutyrine" EXACT UniProt-feature []
-synonym: "phospholosst" EXACT OMSSA-label []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 4 H 5 N 1 O 1" xsd:string
-property_value: MassAvg "83.09" xsd:float
-property_value: MassMono "83.037114" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:23
-xref: uniprot.ptm:PTM-0007
-is_a: MOD:00416
-is_a: MOD:00917
-is_a: MOD:01703
-
-[Term]
-id: MOD:00191
-name: (Z)-2,3-didehydrotyrosine
-def: "A protein modification that effectively converts L-tyrosine to (Z)-2,3-didehydrotyrosine." [PubMed:1347277, PubMed:9631087, RESID:AA0183]
-comment: incidental to RESID:AA0184; incidental to RESID:AA0187; incidental to RESID:AA0188; incidental to RESID:AA0189; incidental to RESID:AA0378; incidental to RESID:AA0379; incidental to RESID:AA0380; incidental to RESID:AA0381
-subset: PSI-MOD-slim
-synonym: "(2Z)-2-amino-3-(4-hydroxyphenyl)prop-2-enoic acid" EXACT RESID-systematic []
-synonym: "(Z)-2,3-didehydrogenated tyrosine" EXACT PSI-MOD-alternate []
-synonym: "(Z)-2,3-didehydrotyrosine" EXACT RESID-name []
-synonym: "2-amino-3-oxo-butanoic_acid" RELATED Unimod-description []
-synonym: "amino-(para-hydroxybenzylidenyl)acetic acid" EXACT RESID-alternate []
-synonym: "cis-dehydrotyrosine" EXACT RESID-alternate []
-synonym: "Didehydro" RELATED PSI-MS-label []
-synonym: "green fluorescent protein chromophore" EXACT RESID-alternate []
-synonym: "MOD_RES (Z)-2,3-didehydrotyrosine" EXACT UniProt-feature []
-synonym: "para-hydroxybenzylidene-imidazolidinone chromophore" EXACT RESID-alternate []
-synonym: "red fluorescent protein chromophore" EXACT RESID-alternate []
-synonym: "Z-dHTyr" EXACT PSI-MOD-label []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 9 H 7 N 1 O 2" xsd:string
-property_value: MassAvg "161.16" xsd:float
-property_value: MassMono "161.047678" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0002
-is_a: MOD:00706
-
-[Term]
-id: MOD:00192
-name: L-serine 5-imidazolinone glycine
-def: "A protein modification that effectively crosslinks an L-serine residue and a glycine residue to form L-serine 5-imidazolinone glycine." [ChEBI:21393, PubMed:1347277, PubMed:9631087, RESID:AA0184]
-comment: Cross-link 2; carboxamidine; incidental to RESID:AA0183; incidental to RESID:AA0365.
-synonym: "(2-[(1R)-1-amino-2-hydroxyethyl]-5-oxo-4,5-dihydro-1H-imidazol-1-yl)acetic acid" EXACT RESID-systematic []
-synonym: "2-[1-amino-2-hydroxyethyl]-1-carboxymethyl-1-imidazolin-5-one" EXACT RESID-alternate []
-synonym: "4-methylidene-imidazole-5-one (MIO) active site" EXACT RESID-alternate []
-synonym: "CROSSLNK 5-imidazolinone (Ser-Gly)" EXACT UniProt-feature []
-synonym: "green fluorescent protein chromophore" EXACT RESID-alternate []
-synonym: "L-serine 5-imidazolinone glycine" EXACT RESID-name []
-synonym: "para-hydroxybenzylidene-imidazolidinone chromophore" EXACT RESID-alternate []
-synonym: "seryl-5-imidazolinone glycine" EXACT RESID-alternate []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 5 H 6 N 2 O 2" xsd:string
-property_value: MassAvg "126.11" xsd:float
-property_value: MassMono "126.042927" xsd:float
-property_value: Origin "G, S" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0049
-is_a: MOD:02047
-is_a: MOD:02055
-is_a: MOD:01882
-is_a: MOD:00954
-
-[Term]
-id: MOD:00193
-name: L-3-oxoalanine (Cys)
-def: "A protein modification that effectively converts an L-cysteine residue to L-oxoalanine." [DeltaMass:350, PubMed:14563551, PubMed:7628016, PubMed:8681943, PubMed:9478923, RESID:AA0185#CYS, Unimod:402#C]
-subset: PSI-MOD-slim
-synonym: "(S)-2-amino-3-oxopropanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-3-oxopropionic acid" EXACT RESID-alternate []
-synonym: "C(alpha)-formylglycine" RELATED RESID-misnomer []
-synonym: "L-3-oxoalanine" EXACT RESID-name []
-synonym: "L-amino-malonic acid semialdehyde" EXACT RESID-alternate []
-synonym: "L-aminomalonaldehydic acid" EXACT RESID-alternate []
-synonym: "L-serinesemialdehyde" RELATED RESID-misnomer []
-synonym: "MOD_RES 3-oxoalanine (Cys)" EXACT UniProt-feature []
-synonym: "Oxala(Cys)" EXACT PSI-MOD-label []
-property_value: DiffAvg "-18.08" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 1 S -1" xsd:string
-property_value: DiffMono "-17.992806" xsd:float
-property_value: Formula "C 3 H 3 N 1 O 2" xsd:string
-property_value: MassAvg "85.06" xsd:float
-property_value: MassMono "85.016378" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:402
-xref: uniprot.ptm:PTM-0034
-is_a: MOD:01169
-
-[Term]
-id: MOD:00194
-name: lactic acid
-def: "A protein modification that effectively converts an L-serine residue to an amino-terminal lactic acid." [PubMed:7607233, RESID:AA0186, Unimod:403#S]
-synonym: "(2R)-2-hydroxypropanoic acid" EXACT RESID-systematic []
-synonym: "2-hydroxypropionic acid" EXACT RESID-alternate []
-synonym: "alpha-hydroxypropionic acid" EXACT RESID-alternate []
-synonym: "Lac(Ser)" EXACT PSI-MOD-label []
-synonym: "lactic acid" EXACT RESID-name []
-synonym: "lactic acid from N-term Ser" RELATED Unimod-description []
-synonym: "MOD_RES Lactic acid" EXACT UniProt-feature []
-synonym: "Ser->LacticAcid" RELATED PSI-MS-label []
-property_value: DiffAvg "-15.02" xsd:float
-property_value: DiffFormula "C 0 H -1 N -1 O 0" xsd:string
-property_value: DiffMono "-15.010899" xsd:float
-property_value: Formula "C 3 H 5 O 2" xsd:string
-property_value: MassAvg "73.07" xsd:float
-property_value: MassMono "73.028954" xsd:float
-property_value: Origin "S" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:403
-xref: uniprot.ptm:PTM-0163
-is_a: MOD:00916
-
-[Term]
-id: MOD:00195
-name: L-alanine 5-imidazolinone glycine
-def: "A protein modification that effectively crosslinks an L-alanine residue and a glycine residue to form L-alanine 5-imidazolinone glycine." [PubMed:10220322, RESID:AA0187]
-comment: Cross-link 2; carboxamidine; incidental to RESID:AA0181; incidental to RESID:AA0183; incidental to RESID:AA0365.
-synonym: "(2-[(1S)-1-aminoethyl]-5-oxo-4,5-dihydro-1H-imidazol-1-yl)acetic acid" EXACT RESID-systematic []
-synonym: "2-[1-aminoethyl]-1-carboxymethyl-1-imidazolin-5-one" EXACT RESID-alternate []
-synonym: "4-methylidene-imidazole-5-one active site" EXACT RESID-alternate []
-synonym: "alanyl-5-imidazolinone glycine" EXACT RESID-alternate []
-synonym: "CROSSLNK 5-imidazolinone (Ala-Gly)" EXACT UniProt-feature []
-synonym: "L-alanine 5-imidazolinone glycine" EXACT RESID-name []
-synonym: "para-hydroxybenzylidene-imidazolidinone chromophore" EXACT RESID-alternate []
-synonym: "XLNK-1Ala-NGly(Imidazole)" EXACT PSI-MOD-label []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 5 H 6 N 2 O 1" xsd:string
-property_value: MassAvg "110.12" xsd:float
-property_value: MassMono "110.048013" xsd:float
-property_value: Origin "A, G" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0045
-is_a: MOD:02040
-is_a: MOD:02047
-is_a: MOD:01882
-is_a: MOD:00954
-
-[Term]
-id: MOD:00196
-name: L-cysteine 5-imidazolinone glycine
-def: "A protein modification that effectively crosslinks an L-cysteine residue and a glycine residue to form L-cysteine 5-imidazolinone glycine." [PubMed:1537807, RESID:AA0188]
-comment: Cross-link 2; carboxamidine; incidental to RESID:AA0181; incidental to RESID:AA0183; incidental to RESID:AA0365.
-synonym: "(2-[(1R)-1-amino-2-sulfanylethyl]-5-oxo-4,5-dihydro-1H-imidazol-1-yl)acetic acid" EXACT RESID-systematic []
-synonym: "2-[1-amino-2-sulfanylethyl]-1-carboxymethyl-1-imidazolin-5-one" EXACT RESID-alternate []
-synonym: "4-methylidene-imidazole-5-one (MIO) active site" EXACT RESID-alternate []
-synonym: "CROSSLNK 5-imidazolinone (Cys-Gly)" EXACT UniProt-feature []
-synonym: "cysteinyl-5-imidazolinone glycine" EXACT RESID-alternate []
-synonym: "L-cysteine 5-imidazolinone glycine" EXACT RESID-name []
-synonym: "para-hydroxybenzylidene-imidazolidinone chromophore" EXACT RESID-alternate []
-synonym: "XLNK-1Cys-NGly(Imidazole)" EXACT PSI-MOD-label []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 5 H 6 N 2 O 1 S 1" xsd:string
-property_value: MassAvg "142.18" xsd:float
-property_value: MassMono "142.020084" xsd:float
-property_value: Origin "C, G" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0047
-is_a: MOD:02044
-is_a: MOD:02047
-is_a: MOD:01882
-is_a: MOD:00954
-
-[Term]
-id: MOD:00197
-name: 2-imino-glutamine 5-imidazolinone glycine
-def: "A protein modification that effectively crosslinks an L-glutamine residue and a glycine residue to form 2-imino-glutamine 5-imidazolinone glycine." [PubMed:11050230, PubMed:11209050, RESID:AA0189]
-comment: Cross-link 2; carboxamidine; incidental to RESID:AA0183; incidental to RESID:AA0365.
-synonym: "2,N-didehydroglutaminyl-5-imidazolinone glycine" EXACT RESID-alternate []
-synonym: "2-(3-carbamoyl-1-imino-propyl)-1-carboxymethyl-1-imidazolin-5-one" EXACT RESID-alternate []
-synonym: "2-imino-glutamine 5-imidazolinone glycine" EXACT RESID-name []
-synonym: "[2-(3-carbamoyl-1-imino-propyl)-5-oxo-4,5-dihydro-imidazol-1-yl]-acetic acid" EXACT RESID-alternate []
-synonym: "[2-(4-amino-4-oxobutanimidoyl)-5-oxo-4,5-dihydro-1H-imidazol-1-yl]acetic acid" EXACT RESID-systematic []
-synonym: "CROSSLNK 2-iminomethyl-5-imidazolinone (Gln-Gly)" EXACT UniProt-feature []
-synonym: "fluorescent protein FP583 chromophore" EXACT RESID-alternate []
-synonym: "para-hydroxybenzylidene-imidazolidinone chromophore" EXACT RESID-alternate []
-synonym: "red fluorescent protein chromophore" EXACT RESID-alternate []
-property_value: DiffAvg "-20.03" xsd:float
-property_value: DiffFormula "C 0 H -4 N 0 O -1" xsd:string
-property_value: DiffMono "-20.026215" xsd:float
-property_value: Formula "C 7 H 7 N 3 O 2" xsd:string
-property_value: MassAvg "165.15" xsd:float
-property_value: MassMono "165.053826" xsd:float
-property_value: Origin "G, Q" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0013
-is_a: MOD:02046
-is_a: MOD:02047
-is_a: MOD:01882
-
-[Term]
-id: MOD:00198
-name: D-alanine (Ala)
-def: "A protein modification that effectively converts an L-alanine residue to D-alanine." [PubMed:15023056, PubMed:7287302, PubMed:7961627, RESID:AA0191#ALA]
-synonym: "(R)-2-aminopropanoic acid" EXACT RESID-systematic []
-synonym: "D-Ala(Ala)" EXACT PSI-MOD-label []
-synonym: "D-alanine" EXACT RESID-name []
-synonym: "MOD_RES D-alanine (Ala)" EXACT UniProt-feature []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 3 H 5 N 1 O 1" xsd:string
-property_value: MassAvg "71.08" xsd:float
-property_value: MassMono "71.037114" xsd:float
-property_value: Origin "A" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0112
-is_a: MOD:00570
-is_a: MOD:00862
-is_a: MOD:00901
-
-[Term]
-id: MOD:00199
-name: D-allo-isoleucine
-def: "A protein modification that effectively converts an L-isoleucine residue to a D-allo-isoleucine." [ChEBI:30007, PubMed:8223491, RESID:AA0192]
-synonym: "(2R,3S)-2-amino-3-methylpentanoic acid" EXACT RESID-systematic []
-synonym: "2-azanyl-3-methylpentanoic acid" EXACT RESID-alternate []
-synonym: "3-methyl-norvaline" EXACT RESID-alternate []
-synonym: "allo-D-isoleucine" EXACT RESID-alternate []
-synonym: "alpha-amino-beta-methylvaleric acid" EXACT RESID-alternate []
-synonym: "D-allo-isoleucine" EXACT RESID-name []
-synonym: "D-Ile" EXACT PSI-MOD-label []
-synonym: "D-threo-isoleucine" EXACT RESID-alternate []
-synonym: "MOD_RES D-allo-isoleucine" EXACT UniProt-feature []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 6 H 11 N 1 O 1" xsd:string
-property_value: MassAvg "113.16" xsd:float
-property_value: MassMono "113.084064" xsd:float
-property_value: Origin "I" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0114
-is_a: MOD:00306
-is_a: MOD:00664
-is_a: MOD:00910
-
-[Term]
-id: MOD:00200
-name: D-methionine
-def: "A protein modification that effectively converts an L-methionine residue to D-methionine." [ChEBI:29984, PubMed:16033333, PubMed:2542051, RESID:AA0193]
-synonym: "(2R)-2-amino-4-(methylsulfanyl)butanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-4-(methylthio)butanoic acid" EXACT RESID-alternate []
-synonym: "2-amino-4-(methylthio)butyric acid" EXACT RESID-alternate []
-synonym: "D-Met" EXACT PSI-MOD-label []
-synonym: "D-methionine" EXACT RESID-name []
-synonym: "MOD_RES D-methionine" EXACT UniProt-feature []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 5 H 9 N 1 O 1 S 1" xsd:string
-property_value: MassAvg "131.19" xsd:float
-property_value: MassMono "131.040485" xsd:float
-property_value: Origin "M" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0120
-is_a: MOD:00664
-is_a: MOD:00913
-
-[Term]
-id: MOD:00201
-name: D-phenylalanine
-def: "A protein modification that effectively converts an L-phenylalanine residue to D-phenylalanine." [ChEBI:29996, PubMed:1548227, PubMed:1644179, PubMed:2597281, RESID:AA0194]
-synonym: "(R)-2-amino-3-phenylpropanoic acid" EXACT RESID-systematic []
-synonym: "D-Phe" EXACT PSI-MOD-label []
-synonym: "D-phenylalanine" EXACT RESID-name []
-synonym: "MOD_RES D-phenylalanine" EXACT UniProt-feature []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 9 H 9 N 1 O 1" xsd:string
-property_value: MassAvg "147.18" xsd:float
-property_value: MassMono "147.068414" xsd:float
-property_value: Origin "F" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0121
-is_a: MOD:00664
-is_a: MOD:00914
-
-[Term]
-id: MOD:00202
-name: D-serine (Ser)
-def: "A protein modification that effectively converts an L-serine residue to D-serine." [PubMed:7973665, RESID:AA0195#SER]
-synonym: "(R)-2-amino-3-hydroxypropanoic acid" EXACT RESID-systematic []
-synonym: "D-Ser(Ser)" EXACT PSI-MOD-label []
-synonym: "D-serine" EXACT RESID-name []
-synonym: "MOD_RES D-serine (Ser)" EXACT UniProt-feature []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 3 H 5 N 1 O 2" xsd:string
-property_value: MassAvg "87.08" xsd:float
-property_value: MassMono "87.032028" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0308
-is_a: MOD:00891
-is_a: MOD:00916
-
-[Term]
-id: MOD:00203
-name: D-asparagine
-def: "A protein modification that effectively converts an L-asparagine residue to D-asparagine." [ChEBI:29957, PubMed:1859408, RESID:AA0196]
-synonym: "(R)-2-amino-4-butanediamic acid" EXACT RESID-systematic []
-synonym: "D-alpha-aminosuccinamic acid" EXACT RESID-alternate []
-synonym: "D-Asn" EXACT PSI-MOD-label []
-synonym: "D-asparagine" EXACT RESID-name []
-synonym: "D-aspartic acid beta-amide" EXACT RESID-alternate []
-synonym: "MOD_RES D-asparagine" EXACT UniProt-feature []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 4 H 6 N 2 O 2" xsd:string
-property_value: MassAvg "114.10" xsd:float
-property_value: MassMono "114.042927" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0115
-is_a: MOD:00664
-is_a: MOD:00903
-
-[Term]
-id: MOD:00204
-name: D-leucine
-def: "A protein modification that effectively converts an L-leucine residue to D-leucine." [ChEBI:30005, PubMed:10461743, PubMed:12135762, PubMed:1358533, PubMed:1548227, RESID:AA0197]
-synonym: "(2R)-2-amino-4-methylpentanoic acid" EXACT RESID-systematic []
-synonym: "alpha-aminoisocaproic acid" EXACT RESID-alternate []
-synonym: "D-Leu" EXACT PSI-MOD-label []
-synonym: "D-leucine" EXACT RESID-name []
-synonym: "MOD_RES D-leucine" EXACT UniProt-feature []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 6 H 11 N 1 O 1" xsd:string
-property_value: MassAvg "113.16" xsd:float
-property_value: MassMono "113.084064" xsd:float
-property_value: Origin "L" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0119
-is_a: MOD:00306
-is_a: MOD:00664
-is_a: MOD:00911
-
-[Term]
-id: MOD:00205
-name: D-tryptophan
-def: "A protein modification that effectively converts an L-tryptophan residue to D-tryptophan." [ChEBI:29955, PubMed:8910408, RESID:AA0198]
-synonym: "(R)-2-amino-3-(1H-indol-3-yl)propanoic acid" EXACT RESID-systematic []
-synonym: "alpha-amino-beta-(3-indolyl)propionoic acid" EXACT RESID-alternate []
-synonym: "D-Trp" EXACT PSI-MOD-label []
-synonym: "D-tryptophan" EXACT RESID-name []
-synonym: "MOD_RES D-tryptophan" EXACT UniProt-feature []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 11 H 10 N 2 O 1" xsd:string
-property_value: MassAvg "186.21" xsd:float
-property_value: MassMono "186.079313" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0123
-is_a: MOD:00664
-is_a: MOD:00918
-
-[Term]
-id: MOD:00206
-name: L-isoglutamyl-polyglycine
-def: "A protein modification that effectively converts an L-glutamic acid residue to L-isoglutamyl-polyglycine." [ChEBI:21343, PubMed:10074368, PubMed:16368691, PubMed:7992051, RESID:AA0201]
-synonym: "gamma-glutamylpolyglycine" EXACT RESID-alternate []
-synonym: "L-isoglutamyl-polyglycine" EXACT RESID-name []
-synonym: "MOD_RES 5-glutamyl polyglycine" EXACT UniProt-feature []
-property_value: Origin "E" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0394
-is_a: MOD:00906
-
-[Term]
-id: MOD:00207
-name: L-isoglutamyl-polyglutamic acid
-def: "A protein modification that effectively converts an L-glutamic acid residue to isoglutamyl-polyglutamic acid, forming an isopeptide bond with a polyglutamic acid." [PubMed:10747868, PubMed:1680872, RESID:AA0202]
-synonym: "gamma-glutamylpolyglutamic acid" EXACT RESID-alternate []
-synonym: "L-isoglutamyl-polyglutamic acid" EXACT RESID-name []
-property_value: Origin "E" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0395
-is_a: MOD:00906
-
-[Term]
-id: MOD:00208
-name: O4'-(phospho-5'-adenosine)-L-tyrosine
-def: "A protein modification that effectively crosslinks an L-tyrosine residue and 5'-phosphoadenosine through a phosphodiester bond to form O4'-(phospho-5'-adenosine)-L-tyrosine." [DeltaMass:0, PubMed:5543675, RESID:AA0203, Unimod:405#Y]
-comment: From DeltaMass: Average Mass: 329.
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-[4-(5'-adenosine phosphonoxy)phenyl]propanoic acid" EXACT RESID-systematic []
-synonym: "5'-adenylic-O-tyrosine" EXACT RESID-alternate []
-synonym: "AMP binding site" RELATED Unimod-description []
-synonym: "hydrogen 5'-adenylate tyrosine ester" EXACT RESID-alternate []
-synonym: "MOD_RES O-AMP-tyrosine" EXACT UniProt-feature []
-synonym: "O-5'-Adenosylation ( of Tyrosine)" EXACT DeltaMass-label []
-synonym: "O4'-(phospho-5'-adenosine)-L-tyrosine" EXACT RESID-name []
-synonym: "O4'-L-tyrosine 5'-adenosine phosphodiester" EXACT RESID-alternate []
-synonym: "OAMPTyr" EXACT PSI-MOD-label []
-synonym: "Phosphoadenosine" RELATED PSI-MS-label []
-property_value: DiffAvg "329.21" xsd:float
-property_value: DiffFormula "C 10 H 12 N 5 O 6 P 1" xsd:string
-property_value: DiffMono "329.052520" xsd:float
-property_value: Formula "C 19 H 21 N 6 O 8 P 1" xsd:string
-property_value: MassAvg "492.38" xsd:float
-property_value: MassMono "492.115848" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:405
-xref: uniprot.ptm:PTM-0332
-is_a: MOD:00919
-is_a: MOD:01165
-
-[Term]
-id: MOD:00209
-name: S-(2-aminovinyl)-D-cysteine (Cys-Ser)
-def: "A protein modification that effectively cross-links an L-cysteine residue and an L-serine residue by a thioether bond to form S-(2-aminovinyl)-D-cysteine." [PubMed:3181159, PubMed:3769923, RESID:AA0204#SER]
-comment: Cross-link 2.
-synonym: "(2S)-2-amino-3-([(Z)-2-aminoethenyl]sulfanyl)propanoic acid" EXACT RESID-systematic []
-synonym: "(S,Z)-S-(2-aminovinyl)cysteine" EXACT RESID-alternate []
-synonym: "CROSSLNK S-(2-aminovinyl)-D-cysteine (Ser-Cys)" EXACT UniProt-feature []
-synonym: "S-(2-aminovinyl)-D-cysteine" EXACT RESID-name []
-synonym: "XLNK-(D)SCys-VinAm" EXACT PSI-MOD-label []
-property_value: DiffAvg "-64.04" xsd:float
-property_value: DiffFormula "C -1 H -4 N 0 O -3 S 0" xsd:string
-property_value: DiffMono "-64.016044" xsd:float
-property_value: Formula "C 5 H 7 N 2 O 1 S 1" xsd:string
-property_value: MassAvg "143.18" xsd:float
-property_value: MassMono "143.027909" xsd:float
-property_value: Origin "C, S" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0268
-is_a: MOD:02055
-is_a: MOD:01850
-
-[Term]
-id: MOD:00210
-name: L-cysteine sulfenic acid
-def: "A protein modification that effectively monooxygenates an L-cysteine residue to L-cysteine sulfenic acid." [DeltaMass:41, OMSSA:193, PubMed:10964927, PubMed:2501303, PubMed:8756456, PubMed:9214307, PubMed:9586994, PubMed:9587003, RESID:AA0205, Unimod:35#C]
-comment: From DeltaMass: Average Mass: 16 Average Mass Change:16 Notes:Green et al. in J. B. C. 270, 18209-18211 (1995) quote Kim and Raines in Eur. J. Biochem. 224, 109-114 (1994). Kim and Raines using ESI-MS and sulfhydryl group titration found that bovine seminal ribonuclease contains a single oxidized sulfhydryl group, which cannot participate in a disulfide bond. This form of cysteine is called sulfenic acid (-SOH).
-subset: PSI-MOD-slim
-synonym: "(2R)-2-amino-3-(hydroxysulfanyl)propanoic acid" EXACT RESID-systematic []
-synonym: "(2R)-2-amino-3-(oxido-lambda(4)-sulfanyl)propanoic acid [tautomer]" EXACT RESID-alternate []
-synonym: "2-amino-2-carboxyethanesulfenic acid" EXACT RESID-alternate []
-synonym: "2-amino-3-sulfinylpropanoic acid [tautomer]" EXACT RESID-alternate []
-synonym: "3-sulfenoalanine" EXACT RESID-alternate []
-synonym: "ACT_SITE Cysteine sulfenic acid (-SOH) intermediate" EXACT UniProt-feature []
-synonym: "CysOH" EXACT PSI-MOD-label []
-synonym: "cysteine S-oxide [tautomer]" EXACT RESID-alternate []
-synonym: "cysteine sulfoxide [tautomer]" EXACT RESID-alternate []
-synonym: "cysteine sulphenic acid" EXACT RESID-alternate []
-synonym: "L-cysteine sulfenic acid" EXACT RESID-name []
-synonym: "mod193" EXACT OMSSA-label []
-synonym: "MOD_RES Cysteine sulfenic acid (-SOH)" EXACT UniProt-feature []
-synonym: "Oxidation" RELATED PSI-MS-label []
-synonym: "S-hydroxycysteine" EXACT RESID-alternate []
-synonym: "S-oxocysteine [tautomer]" EXACT RESID-alternate []
-synonym: "S-oxycysteine [tautomer]" EXACT RESID-alternate []
-synonym: "Sulfenic Acid (from Cysteine)" EXACT DeltaMass-label []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1 S 0" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 3 H 5 N 1 O 2 S 1" xsd:string
-property_value: MassAvg "119.14" xsd:float
-property_value: MassMono "119.004099" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:35
-xref: uniprot.ptm:PTM-0107
-is_a: MOD:00708
-is_a: MOD:01854
-
-[Term]
-id: MOD:00211
-name: S-(glycyl)-L-cysteine (Cys-Gly)
-def: "A protein modification that effectively crosslinks an L-cysteine residue and a glycine residue by a thioester bond to form S-glycyl-L-cysteine." [ChEBI:22050, PubMed:3306404, RESID:AA0206]
-comment: Cross-link 2. For the modification of a C-terminal glycine by formation of a thioester bond with free L-cysteine see MOD:01777 [JSG].
-subset: PSI-MOD-slim
-synonym: "(2R)-2-amino-3-[(aminoacetyl)sulfanyl]propanoic acid" EXACT RESID-systematic []
-synonym: "1-(cystein-S-yl)-glycinate" EXACT RESID-alternate []
-synonym: "ACT_SITE Glycyl thioester intermediate" EXACT UniProt-feature []
-synonym: "glycine cysteine thioester" EXACT RESID-alternate []
-synonym: "S-(2-amino-1-oxoethyl)cysteine" EXACT RESID-alternate []
-synonym: "S-(glycyl)-L-cysteine" EXACT RESID-name []
-synonym: "XLNK-SCys-1Gly" EXACT PSI-MOD-label []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 5 H 7 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "159.18" xsd:float
-property_value: MassMono "159.022823" xsd:float
-property_value: Origin "C, G" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0429
-is_a: MOD:00395
-is_a: MOD:02047
-is_a: MOD:00954
-
-[Term]
-id: MOD:00212
-name: S-4-hydroxycinnamyl-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-4-hydroxycinnamyl-L-cysteine." [PubMed:7947803, PubMed:7981196, RESID:AA0207, Unimod:407]
-synonym: "(2R)-2-amino-3-([(2E)-3-(4-hydroxyphenyl)prop-2-enoyl]sulfanyl)propanoic acid" EXACT RESID-systematic []
-synonym: "cinnamate cysteine thioester" EXACT RESID-alternate []
-synonym: "Hydroxycinnamyl" RELATED PSI-MS-label []
-synonym: "hydroxycinnamyl" RELATED Unimod-description []
-synonym: "MOD_RES S-(4-hydroxycinnamyl)cysteine" EXACT UniProt-feature []
-synonym: "S-4-hydroxycinnamyl-L-cysteine" EXACT RESID-name []
-synonym: "S-para-coumaryl-L-cysteine" EXACT RESID-alternate []
-property_value: DiffAvg "146.14" xsd:float
-property_value: DiffFormula "C 9 H 6 N 0 O 2 S 0" xsd:string
-property_value: DiffMono "146.036779" xsd:float
-property_value: Formula "C 12 H 11 N 1 O 3 S 1" xsd:string
-property_value: MassAvg "249.28" xsd:float
-property_value: MassMono "249.045964" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:407
-xref: uniprot.ptm:PTM-0414
-is_a: MOD:00905
-
-[Term]
-id: MOD:00213
-name: chondroitin sulfate D-glucuronosyl-D-galactosyl-D-galactosyl-D-xylosyl-L-serine
-def: "A protein modification that effectively cross-links an L-serine residue to the polymer chondroitin sulfate by a D-glucuronosyl-D-galactosyl-D-galactosyl-D-xylosyl tetrasaccharide." [PubMed:1794445, PubMed:1898736, PubMed:3472204, RESID:AA0208]
-synonym: "chondroitin 4-sulfate (chondroitin sulfate A)" EXACT RESID-alternate []
-synonym: "chondroitin 6-sulfate (chondroitin sulfate C)" EXACT RESID-alternate []
-synonym: "chondroitin sulfate D-glucuronosyl-D-galactosyl-D-galactosyl-D-xylosyl-L-serine" EXACT RESID-name []
-synonym: "poly[beta-1,4-D-glucopyranuronosyl-beta-1,3-(2-acetamido-2-deoxy-4-sulfate-D-galactosyl)]-beta-1,4-D-glucopyranuronosyl-beta-1,3-D-galactosyl-beta-1,3-D-galactosyl-beta-1,4-D-xylosyl-beta-1,3-L-serine; poly[beta-1,4-D-glucopyranuronosyl-beta-1,3-(2-acetamido-2-deoxy-6-sulfate D-galactosyl)]-beta-1,4-D-glucopyranuronosyl-beta-1,3-D-galactosyl-beta-1,3-D-galactosyl-beta-1,4-D-xylosyl-beta-1,3-L-serine" EXACT RESID-systematic []
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00002
-
-[Term]
-id: MOD:00214
-name: dermatan 4-sulfate D-glucuronosyl-D-galactosyl-D-galactosyl-D-xylosyl-L-serine
-def: "A protein modification that effectively cross-links an L-serine residue to the polymer dermatan 4-sulfate by a D-glucuronosyl-D-galactosyl-D-galactosyl-D-xylosyl tetrasaccharide." [PubMed:2914936, PubMed:3472204, RESID:AA0209]
-synonym: "beta-heparin" EXACT RESID-alternate []
-synonym: "chondroitin sulfate B" EXACT RESID-alternate []
-synonym: "dermatan 4-sulfate D-glucuronosyl-D-galactosyl-D-galactosyl-D-xylosyl-L-serine" EXACT RESID-name []
-synonym: "poly[beta-1,4-L-idopyranuronosyl-alpha-1,3-(2-acetamido-2-deoxy-4-sulfate D-galactosyl)]-beta-1,4-D-glucopyranuronosyl-beta-1,3-D-galactosyl-beta-1,3-D-galactosyl-beta-1,4-D-xylosyl-beta-1,3-L-serine" EXACT RESID-systematic []
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00002
-
-[Term]
-id: MOD:00215
-name: heparan sulfate D-glucuronosyl-D-galactosyl-D-galactosyl-D-xylosyl-L-serine
-def: "A protein modification that effectively cross-links an L-serine residue to the polymer heparan sulfate by a D-glucuronosyl-D-galactosyl-D-galactosyl-D-xylosyl tetrasaccharide." [PubMed:3472204, RESID:AA0210]
-synonym: "heparan sulfate D-glucuronosyl-D-galactosyl-D-galactosyl-D-xylosyl-L-serine" EXACT RESID-name []
-synonym: "heparin" EXACT RESID-alternate []
-synonym: "heparitin sulfate" EXACT RESID-alternate []
-synonym: "poly[alpha-1,4-(2-sulfate D-glucopyranuronosyl)-beta-1,4-(2-sulfamino-2-deoxy-6-sulfate D-glucosyl)]-beta-1,4-D-glucopyranuronosyl-beta-1,3-D-galactosyl-beta-1,3-D-galactosyl-beta-1,4-D-xylosyl-beta-1,3-L-serine" EXACT RESID-systematic []
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00002
-
-[Term]
-id: MOD:00216
-name: N6-formyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-formyl-L-lysine." [OMSSA:43, PubMed:15799070, RESID:AA0211, Unimod:122#K]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-6-(formylamino)hexanoic acid" EXACT RESID-systematic []
-synonym: "epsilon-formyllysine" EXACT RESID-alternate []
-synonym: "Formyl" RELATED PSI-MS-label []
-synonym: "Formylation" RELATED Unimod-description []
-synonym: "formylk" EXACT OMSSA-label []
-synonym: "MOD_RES N6-formyllysine" EXACT UniProt-feature []
-synonym: "N(zeta)-formyllysine" EXACT RESID-alternate []
-synonym: "N6-formyl-L-lysine" EXACT RESID-name []
-synonym: "N6-formylated L-lysine" EXACT PSI-MOD-alternate []
-synonym: "N6FoLys" EXACT PSI-MOD-label []
-property_value: DiffAvg "28.01" xsd:float
-property_value: DiffFormula "C 1 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "27.994915" xsd:float
-property_value: Formula "C 7 H 12 N 2 O 2" xsd:string
-property_value: MassAvg "156.19" xsd:float
-property_value: MassMono "156.089878" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:122
-xref: uniprot.ptm:PTM-0192
-is_a: MOD:00409
-is_a: MOD:01875
-
-[Term]
-id: MOD:00217
-name: O4-arabinosyl-L-hydroxyproline
-def: "A protein modification that effectively converts an L-proline residue to O4-arabinosyl-L-hydroxyproline." [DeltaMass:0, PubMed:666730, PubMed:7852316, RESID:AA0212, Unimod:408]
-comment: secondary to RESID:AA0030; From DeltaMass: Average Mass: 147.
-subset: PSI-MOD-slim
-synonym: "(2S,4R)-4-(beta-L-arabinofuranosyloxy)pyrrolidine-2-carboxylic acid" EXACT RESID-systematic []
-synonym: "4-(beta-L-arabinofuranosyloxy)proline" EXACT RESID-alternate []
-synonym: "4-Glycosyloxy- (pentosyl,C5) (of Proline)" EXACT DeltaMass-label []
-synonym: "beta-arabinofuranosyl-4-hydroxyproline" EXACT RESID-alternate []
-synonym: "Glycosyl" RELATED PSI-MS-label []
-synonym: "glycosyl-L-hydroxyproline" RELATED Unimod-description []
-synonym: "O4-arabinosyl-L-hydroxyproline" EXACT RESID-name []
-synonym: "O4-glycosyl-hydroxyproline" EXACT RESID-alternate []
-synonym: "OAra4HyPro" EXACT PSI-MOD-label []
-property_value: DiffAvg "148.11" xsd:float
-property_value: DiffFormula "C 5 H 8 N 0 O 5" xsd:string
-property_value: DiffMono "148.037173" xsd:float
-property_value: Formula "C 10 H 15 N 1 O 6" xsd:string
-property_value: MassAvg "245.23" xsd:float
-property_value: MassMono "245.089937" xsd:float
-property_value: Origin "P" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:408
-xref: uniprot.ptm:PTM-0545
-is_a: MOD:00396
-is_a: MOD:00915
-
-[Term]
-id: MOD:00218
-name: O-(phospho-5'-RNA)-L-serine
-def: "A protein modification that effectively crosslinks an L-serine residue and the 5'-end of RNA through a phosphodiester to form O4'-(phospho-5'-RNA)-L-serine." [PubMed:1705009, RESID:AA0213]
-synonym: "(S)-2-amino-3-(5'-ribonucleic acid phosphonoxy)propanoic acid" EXACT RESID-systematic []
-synonym: "MOD_RES O-(5'-phospho-RNA)-serine" EXACT UniProt-feature []
-synonym: "O-(phospho-5'-RNA)-L-serine" EXACT RESID-name []
-synonym: "O3-(phospho-5'-RNA)-L-serine" EXACT RESID-alternate []
-synonym: "O3-L-serine 5'-RNA phosphodiester" EXACT RESID-alternate []
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0227
-is_a: MOD:00751
-is_a: MOD:00916
-
-[Term]
-id: MOD:00219
-name: L-citrulline
-def: "A protein modification that effectively converts an L-arginine residue to L-citrulline." [DeltaMass:0, OMSSA:33, PubMed:2466844, RESID:AA0214, Unimod:7#R]
-comment: This modification is not the result of deamidation, instead the guanidino group is replaced with an ureido group.
-subset: PSI-MOD-slim
-synonym: "(S)-2-amino-5-(carbamoylamino)pentanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-5-(aminocarbonyl)aminopentanoic acid" EXACT RESID-alternate []
-synonym: "alpha-amino-delta-ureidovaleric acid" EXACT RESID-alternate []
-synonym: "Cit" EXACT PSI-MOD-label []
-synonym: "citrullinationr" EXACT OMSSA-label []
-synonym: "Citrulline" EXACT DeltaMass-label []
-synonym: "Deamidated" RELATED PSI-MS-label []
-synonym: "Deamidated" RELATED Unimod-interim []
-synonym: "Deamidation" RELATED Unimod-description []
-synonym: "delta-ureidonorvaline" EXACT RESID-alternate []
-synonym: "L-citrulline" EXACT RESID-name []
-synonym: "MOD_RES Citrulline" EXACT UniProt-feature []
-synonym: "N5-(aminocarbonyl)ornithine" EXACT RESID-alternate []
-synonym: "N5-carbamoylornithine" EXACT RESID-alternate []
-synonym: "N5-carbamylornithine" EXACT RESID-alternate []
-property_value: DiffAvg "0.98" xsd:float
-property_value: DiffFormula "C 0 H -1 N -1 O 1" xsd:string
-property_value: DiffMono "0.984016" xsd:float
-property_value: Formula "C 6 H 11 N 3 O 2" xsd:string
-property_value: MassAvg "157.17" xsd:float
-property_value: MassMono "157.085127" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:7
-xref: uniprot.ptm:PTM-0092
-is_a: MOD:00902
-
-[Term]
-id: MOD:00220
-name: 4-hydroxy-L-arginine
-def: "A protein modification that effectively converts an L-arginine residue to a 4-hydroxy-L-arginine." [PubMed:10966817, PubMed:7650037, RESID:AA0215]
-synonym: "(2S,4Xi)-2-amino-5-[(diaminomethylidene)amino]-4-hydroxypentanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-5-(carbamimidamido)-4-hydroxypentanoic acid [tautomer]" EXACT RESID-alternate []
-synonym: "2-amino-5-[(aminoiminomethyl)amino]-4-hydroxypentanoic acid [tautomer]" EXACT RESID-alternate []
-synonym: "2-amino-5-guanidino-4-hydroxypentanoic acid" EXACT RESID-alternate []
-synonym: "4-hydroxy-L-arginine" EXACT RESID-name []
-synonym: "4-hydroxylated L-arginine" EXACT PSI-MOD-alternate []
-synonym: "4HyArg" EXACT PSI-MOD-label []
-synonym: "C(gamma)-hydroxyarginine" EXACT RESID-alternate []
-synonym: "gamma-hydroxyarginine" EXACT RESID-alternate []
-synonym: "MOD_RES 4-hydroxyarginine" EXACT UniProt-feature []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 6 H 12 N 4 O 2" xsd:string
-property_value: MassAvg "172.19" xsd:float
-property_value: MassMono "172.096026" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0042
-is_a: MOD:00425
-is_a: MOD:00682
-
-[Term]
-id: MOD:00221
-name: N-(L-isoaspartyl)-L-cysteine
-def: "A protein modification that effectively crosslinks L-aspartic acid and L-cysteine residues via an isopeptide bond to form N-(L-isoaspartyl)-L-cysteine." [PubMed:8286361, RESID:AA0216]
-comment: Cross-link 2.
-synonym: "(S)-2-amino-4-((R)-1-carboxy-2-sulfanylethyl)amino-4-oxobutanoic acid" EXACT RESID-systematic []
-synonym: "2-(3-amino-3-carboxypropanoyl)amino-3-mercaptopropanoic acid" EXACT RESID-alternate []
-synonym: "2-amino-N4-(1-carboxy-2-mercaptoethyl)butanediamic acid" EXACT RESID-alternate []
-synonym: "CROSSLNK Isoaspartyl cysteine isopeptide (Cys-Asn)" EXACT UniProt-feature []
-synonym: "N-(L-isoaspartyl)-L-cysteine" EXACT RESID-name []
-synonym: "N-beta-aspartylcysteine" EXACT RESID-alternate []
-synonym: "N-isoaspartyl cysteine" EXACT RESID-alternate []
-property_value: DiffAvg "-17.03" xsd:float
-property_value: DiffFormula "C 0 H -3 N -1 O 0 S 0" xsd:string
-property_value: DiffMono "-17.026549" xsd:float
-property_value: Formula "C 7 H 9 N 2 O 3 S 1" xsd:string
-property_value: MassAvg "201.22" xsd:float
-property_value: MassMono "201.033388" xsd:float
-property_value: Origin "C, N" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0151
-is_a: MOD:02042
-is_a: MOD:02044
-is_a: MOD:00946
-is_a: MOD:00688
-
-[Term]
-id: MOD:00222
-name: 2'-alpha-mannosyl-L-tryptophan
-def: "A protein modification that effectively converts an L-tryptophan residue to 2'-alpha-mannosyl-L-tryptophan." [PubMed:15279557, PubMed:7547911, PubMed:7947762, RESID:AA0217, Unimod:41#W]
-synonym: "(2S)-2-amino-3-(2-beta-D-mannopyranosyl-1H-indol-3-yl)propanoic acid" EXACT RESID-systematic []
-synonym: "2'-mannosyl-L-tryptophan" EXACT RESID-name []
-synonym: "2'-tryptophan C-mannoside" EXACT RESID-alternate []
-synonym: "C2'ManTrp" EXACT PSI-MOD-label []
-synonym: "CARBOHYD C-linked (Man) tryptophan" EXACT UniProt-feature []
-synonym: "Hex" RELATED PSI-MS-label []
-synonym: "Hexose" RELATED Unimod-description []
-property_value: DiffAvg "162.14" xsd:float
-property_value: DiffFormula "C 6 H 10 N 0 O 5" xsd:string
-property_value: DiffMono "162.052823" xsd:float
-property_value: Formula "C 17 H 20 N 2 O 6" xsd:string
-property_value: MassAvg "348.36" xsd:float
-property_value: MassMono "348.132136" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:41
-xref: uniprot.ptm:PTM-0505
-is_a: MOD:00421
-is_a: MOD:00595
-is_a: MOD:00918
-
-[Term]
-id: MOD:00223
-name: N6-mureinyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-mureinyl-L-lysine." [PubMed:4261992, RESID:AA0218]
-synonym: "MOD_RES N6-murein peptidoglycan lysine" EXACT UniProt-feature []
-synonym: "N6-[(2R,6S)-2-(N-(N-mureinyl-(R)-alanyl)-(S)-glutamyl)amino-6-amino-6-carboxy-1-oxohex-1-yl]lysine" EXACT RESID-alternate []
-synonym: "N6-mureinyl-L-lysine" EXACT RESID-name []
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0195
-is_a: MOD:01159
-is_a: MOD:01875
-
-[Term]
-id: MOD:00224
-name: 1-chondroitin sulfate-L-aspartic acid ester
-def: "A protein modification that effectively converts an L-aspartic acid residue to 1-chondroitin sulfate-L-aspartic acid ester" [PubMed:1898736, RESID:AA0219]
-synonym: "1-aspartic acid ester with 6-chondroitin 4-sulfate" EXACT RESID-alternate []
-synonym: "1-chondroitin sulfate-L-aspartic acid ester" EXACT RESID-name []
-synonym: "MOD_RES Aspartate 1-(chondroitin 4-sulfate)-ester" EXACT UniProt-feature []
-synonym: "poly[beta-1,4-D-glucopyranuronosyl-beta-1,3-(2-acetamido-2-deoxy-4-sulfate D-galactosyl)]beta-1,4-D-glucopyranuronosyl-beta-1,3-(2-acetamido-2-deoxy-4-sulfate-6-(1-L-aspartyl)-D-galactose)" EXACT RESID-alternate []
-synonym: "protein-glycosaminoglycan-protein cross-link" EXACT RESID-alternate []
-property_value: Origin "D" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0334
-is_a: MOD:00904
-
-[Term]
-id: MOD:00225
-name: S-(6-FMN)-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-(6-FMN)-L-cysteine." [PubMed:10869173, PubMed:1551870, PubMed:620783, RESID:AA0220, Unimod:409#C]
-subset: PSI-MOD-slim
-synonym: "(R)-2-amino-3-[6-riboflavin 5'-dihydrogen phosphate]sulfanylpropanoic acid" EXACT RESID-systematic []
-synonym: "6-[S-cysteinyl]flavin mononucleotide" EXACT RESID-alternate []
-synonym: "6-[S-cysteinyl]FMN" EXACT RESID-alternate []
-synonym: "flavin mononucleotide" RELATED Unimod-description []
-synonym: "FMNH" RELATED PSI-MS-label []
-synonym: "MOD_RES S-6-FMN cysteine" EXACT UniProt-feature []
-synonym: "S-(6-FMN)-L-cysteine" EXACT RESID-name []
-synonym: "S6FMNCys" EXACT PSI-MOD-label []
-property_value: DiffAvg "454.33" xsd:float
-property_value: DiffFormula "C 17 H 19 N 4 O 9 P 1 S 0" xsd:string
-property_value: DiffMono "454.088965" xsd:float
-property_value: Formula "C 20 H 24 N 5 O 10 P 1 S 1" xsd:string
-property_value: MassAvg "557.47" xsd:float
-property_value: MassMono "557.098150" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:409
-xref: uniprot.ptm:PTM-0271
-is_a: MOD:02084
-is_a: MOD:00905
-
-[Term]
-id: MOD:00226
-name: 1'-(8alpha-FAD)-L-histidine
-def: "A protein modification that effectively converts an L-histidine residue to 1'-(8alpha-FAD)-L-histidine." [DeltaMass:0, PubMed:10585424, PubMed:1396672, PubMed:4339951, PubMed:9261083, RESID:AA0221, Unimod:50#H]
-comment: From DeltaMass: Average Mass: 784
-subset: PSI-MOD-slim
-synonym: "(S)-2-amino-3-(1-[8alpha riboflavin 5'-(trihydrogen diphosphate) 5'->5'-ester with adenosine]imidazol-4-yl)propanoic acid" EXACT RESID-systematic []
-synonym: "1'-(8alpha-FAD)-L-histidine" EXACT RESID-name []
-synonym: "8alpha-(N(epsilon)-histidyl)FAD" EXACT RESID-alternate []
-synonym: "8alpha-(N1'-histidyl)FAD" EXACT RESID-alternate []
-synonym: "8alpha-N3-histidyl FAD" RELATED RESID-misnomer []
-synonym: "FAD" RELATED PSI-MS-label []
-synonym: "Flavin adenine dinucleotide" RELATED Unimod-description []
-synonym: "MOD_RES Tele-8alpha-FAD histidine" EXACT UniProt-feature []
-synonym: "N theta and N pi-(8alpha-Flavin) (on Histidine)" EXACT DeltaMass-label []
-synonym: "N(tau)-(8alpha-FAD)-histidine" EXACT RESID-alternate []
-synonym: "Nt8aFADHis" EXACT PSI-MOD-label []
-synonym: "tele-(8alpha-FAD)-histidine" EXACT RESID-alternate []
-property_value: DiffAvg "783.54" xsd:float
-property_value: DiffFormula "C 27 H 31 N 9 O 15 P 2" xsd:string
-property_value: DiffMono "783.141485" xsd:float
-property_value: Formula "C 33 H 38 N 12 O 16 P 2" xsd:string
-property_value: MassAvg "920.68" xsd:float
-property_value: MassMono "920.200396" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:50
-xref: uniprot.ptm:PTM-0288
-is_a: MOD:00895
-is_a: MOD:00909
-
-[Term]
-id: MOD:00227
-name: omega-N-phospho-L-arginine
-def: "A protein modification that effectively converts an L-arginine residue to omega-N-phospho-L-arginine." [PubMed:8300603, RESID:AA0222, Unimod:21#R]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-5-([amino(phosphonoamino)methylidene]amino)pentanoic acid" EXACT RESID-systematic []
-synonym: "(2S)-2-amino-5-(N'-phosphonocarbamimidamido)pentanoic acid" EXACT RESID-alternate []
-synonym: "alpha-amino-delta-phosphonoguanidinovaleric acid" EXACT RESID-alternate []
-synonym: "MOD_RES Phosphoarginine" EXACT UniProt-feature []
-synonym: "N(gamma)-phosphoarginine" EXACT RESID-alternate []
-synonym: "N(omega)-phosphono-L-arginine" EXACT RESID-alternate []
-synonym: "N5-[imino(phosphonoamino)methyl]-L-ornithine" EXACT RESID-alternate []
-synonym: "omega-N-phospho-L-arginine" EXACT RESID-name []
-synonym: "PArg" EXACT PSI-MOD-label []
-synonym: "Phospho" RELATED PSI-MS-label []
-synonym: "phosphoarginine" EXACT RESID-alternate []
-synonym: "Phosphorylation" RELATED Unimod-description []
-property_value: DiffAvg "79.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 0 O 3 P 1" xsd:string
-property_value: DiffMono "79.966331" xsd:float
-property_value: Formula "C 6 H 13 N 4 O 4 P 1" xsd:string
-property_value: MassAvg "236.17" xsd:float
-property_value: MassMono "236.067442" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:21
-xref: uniprot.ptm:PTM-0250
-is_a: MOD:00902
-is_a: MOD:01456
-
-[Term]
-id: MOD:00228
-name: S-diphytanylglycerol diether-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-diphytanylglycerol diether-L-cysteine." [PubMed:7797461, PubMed:8195126, RESID:AA0223, Unimod:410]
-comment: incidental to RESID:AA0043.
-subset: PSI-MOD-slim
-synonym: "(2R)-2-amino-3-([(2S)-2,3-bis(3,7,11,15-tetramethylhexadecanyloxy)propyl]sulfanyl)propanoic acid" EXACT RESID-systematic []
-synonym: "Archaeol" RELATED PSI-MS-label []
-synonym: "LIPID S-archaeol cysteine" EXACT UniProt-feature []
-synonym: "S-(diphytanylglyceryl)-L-cysteine" EXACT RESID-name []
-synonym: "S-[2',3'-bis(phytanyloxy)propyl]cysteine" EXACT RESID-alternate []
-synonym: "S-archaeol cysteine" EXACT RESID-alternate []
-synonym: "S-diphytanylglycerol diether" RELATED Unimod-description []
-synonym: "SPhyt2GlyceroCys" EXACT PSI-MOD-label []
-property_value: DiffAvg "635.16" xsd:float
-property_value: DiffFormula "C 43 H 86 N 0 O 2 S 0" xsd:string
-property_value: DiffMono "634.662782" xsd:float
-property_value: Formula "C 46 H 91 N 1 O 3 S 1" xsd:string
-property_value: MassAvg "738.30" xsd:float
-property_value: MassMono "737.671967" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:410
-xref: uniprot.ptm:PTM-0273
-is_a: MOD:00905
-is_a: MOD:01155
-
-[Term]
-id: MOD:00229
-name: alpha-1-microglobulin-Ig alpha complex chromophore
-def: "A protein modification that effectively converts two L-cysteine residues to form alpha-1-microglobulin-Ig alpha complex chromophore." [PubMed:11058759, PubMed:11877257, PubMed:7506257, PubMed:7535251, RESID:AA0224]
-comment: Cross-link 2.
-synonym: "alpha-1-microglobulin-Ig alpha complex chromophore" EXACT RESID-name []
-synonym: "BINDING Multimeric 3-hydroxykynurenine chromophore (covalent)" EXACT UniProt-feature []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 6 H 8 N 2 O 2 S 2" xsd:string
-property_value: MassAvg "204.26" xsd:float
-property_value: MassMono "204.002720" xsd:float
-property_value: Origin "C, C" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:02044
-
-[Term]
-id: MOD:00230
-name: bis-L-cysteinyl bis-L-histidino diiron disulfide
-def: "A protein modification that effectively converts two L-cysteine residues, two L-histidine residues and a two-iron two-sulfur cluster to bis-L-cysteinyl bis-L-histidino diiron disulfide." [PubMed:2765515, PubMed:9651245, RESID:AA0225]
-comment: Cross-link 4.
-synonym: "bis-L-cysteinyl bis-L-histidino diiron disulfide" EXACT RESID-name []
-synonym: "di-mu-sulfido(bis-S-cysteinyliron)(bis-N3'-histidinoiron)" EXACT RESID-systematic []
-synonym: "METAL Iron-sulfur (2Fe-2S)" EXACT UniProt-feature []
-synonym: "METAL Iron-sulfur (2Fe-2S); via pros nitrogen" EXACT UniProt-feature []
-synonym: "Rieske iron-sulfur cofactor" EXACT RESID-alternate []
-property_value: DiffAvg "171.78" xsd:float
-property_value: DiffFormula "C 0 Fe 2 H -4 N 0 O 0 S 2" xsd:string
-property_value: DiffMono "171.783814" xsd:float
-property_value: FormalCharge "2-" xsd:string
-property_value: Formula "C 18 Fe 2 H 20 N 8 O 4 S 4" xsd:string
-property_value: MassAvg "652.34" xsd:float
-property_value: MassMono "651.920007" xsd:float
-property_value: Origin "C, C, H, H" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00739
-is_a: MOD:02067
-is_a: MOD:02070
-
-[Term]
-id: MOD:00231
-name: hexakis-L-cysteinyl hexairon hexasulfide
-def: "A protein modification that effectively converts six L-cysteine residues and a six-iron six-sulfur cluster to hexakis-L-cysteinyl hexairon hexasulfide." [PubMed:1311311, PubMed:1318833, RESID:AA0226]
-comment: Cross-link 6. This is a deprecated entry in RESID. It probably does not occur naturally [JSG].
-synonym: "hexa-mu3-sulfido-hexakis(cysteinato-kappaS)-hexairon" EXACT RESID-systematic []
-synonym: "hexa-mu3-sulfido-hexakis(S-cysteinyliron)" EXACT RESID-alternate []
-synonym: "hexakis-L-cysteinyl hexairon hexasulfide" EXACT RESID-name []
-synonym: "prismane iron-sulfur cofactor" EXACT RESID-alternate []
-property_value: DiffAvg "521.38" xsd:float
-property_value: DiffFormula "C 0 Fe 6 H -6 N 0 O 0 S 6" xsd:string
-property_value: DiffMono "521.395649" xsd:float
-property_value: FormalCharge "1-" xsd:string
-property_value: Formula "C 18 Fe 6 H 24 N 6 O 6 S 12" xsd:string
-property_value: MassAvg "1140.22" xsd:float
-property_value: MassMono "1139.450758" xsd:float
-property_value: Origin "C, C, C, C, C, C" xsd:string
-property_value: Source "hypothetical" xsd:string
-is_a: MOD:00739
-is_a: MOD:02067
-
-[Term]
-id: MOD:00232
-name: N6-(phospho-5'-adenosine)-L-lysine
-def: "A protein modification that effectively crosslinks an L-lysine residue and 5'-phosphoadenosine through a phosphoramide ester bond to form N6-(phospho-5'-adenosine)-L-lysine." [DeltaMass:316, PubMed:3882425, PubMed:4944632, RESID:AA0227, Unimod:405#K]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-6-(5'-adenosine phosphonamino)hexanoic acid" EXACT RESID-systematic []
-synonym: "5'-adenylic-N6-L-lysine" EXACT RESID-alternate []
-synonym: "ACT_SITE N6-AMP-lysine intermediate" EXACT UniProt-feature []
-synonym: "AMP binding site" RELATED Unimod-description []
-synonym: "AMP Lysyl" EXACT DeltaMass-label []
-synonym: "epsilon-5'-adenylic-L-lysine" EXACT RESID-alternate []
-synonym: "L-lysine monoanhydride with 5'-adenylic acid" EXACT RESID-alternate []
-synonym: "N(zeta)-5'-adenylic-L-lysine" EXACT RESID-alternate []
-synonym: "N6-(phospho-5'-adenosine)-L-lysine" EXACT RESID-name []
-synonym: "N6-L-lysine 5'-adenosine phosphoramidester" EXACT RESID-alternate []
-synonym: "N6AMPLys" EXACT PSI-MOD-label []
-synonym: "Phosphoadenosine" RELATED PSI-MS-label []
-property_value: DiffAvg "329.21" xsd:float
-property_value: DiffFormula "C 10 H 12 N 5 O 6 P 1" xsd:string
-property_value: DiffMono "329.052520" xsd:float
-property_value: Formula "C 16 H 24 N 7 O 7 P 1" xsd:string
-property_value: MassAvg "457.38" xsd:float
-property_value: MassMono "457.147483" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:405
-is_a: MOD:00912
-is_a: MOD:01165
-
-[Term]
-id: MOD:00233
-name: N6-(phospho-5'-guanosine)-L-lysine
-def: "A protein modification that effectively crosslinks an L-lysine residue and 5'-phosphoguanosine through a phosphoramide ester bond to form N6-(phospho-5'-guanosine)-L-lysine." [DeltaMass:304, PubMed:6092377, PubMed:6264433, RESID:AA0228, Unimod:413#K]
-comment: From DeltaMass: Average Mass: 345 Formula:C10H12O5N7P1 Monoisotopic Mass Change:345.047 Average Mass Change:345.209 References:PE Sciex
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-6-(5'-guanosine phosphonamino)hexanoic acid" EXACT RESID-systematic []
-synonym: "5'-guanylic-N6-L-lysine" EXACT RESID-alternate []
-synonym: "5'phos Guanosyl" EXACT DeltaMass-label []
-synonym: "ACT_SITE N6-GMP-lysine intermediate" EXACT UniProt-feature []
-synonym: "epsilon-5'-guanylic-L-lysine" EXACT RESID-alternate []
-synonym: "L-lysine monoanhydride with 5'-guanylic acid" EXACT RESID-alternate []
-synonym: "lysine guanosine-5'-monophosphate" EXACT RESID-alternate []
-synonym: "N(zeta)-5'-guanylic-lysine" EXACT RESID-alternate []
-synonym: "N6-(5'-guanylyl)-lysine" EXACT RESID-alternate []
-synonym: "N6-(phospho-5'-guanosine)-L-lysine" EXACT RESID-name []
-synonym: "N6-L-lysine 5'-guanosine phosphoramidester" EXACT RESID-alternate []
-synonym: "N6GMPLys" EXACT PSI-MOD-label []
-synonym: "phospho-guanosine" RELATED Unimod-description []
-synonym: "Phosphoguanosine" RELATED PSI-MS-label []
-property_value: DiffAvg "345.21" xsd:float
-property_value: DiffFormula "C 10 H 12 N 5 O 7 P 1" xsd:string
-property_value: DiffMono "345.047434" xsd:float
-property_value: Formula "C 16 H 24 N 7 O 8 P 1" xsd:string
-property_value: MassAvg "473.38" xsd:float
-property_value: MassMono "473.142397" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:413
-is_a: MOD:00912
-is_a: MOD:01163
-
-[Term]
-id: MOD:00234
-name: L-cysteine glutathione disulfide
-def: "A protein modification that effectively converts an L-cysteine residue to S-glutathionyl-L-cysteine." [ChEBI:21264, DeltaMass:0, OMSSA:51, PubMed:3083866, PubMed:8344916, RESID:AA0229, Unimod:55]
-comment: From DeltaMass: Average Mass: 305
-comment: Glutamyl-transpeptidase cleaves glutathione into cysteinylglycine (Cys-Gly) and a Glu residue. [PubMed: 28537416]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-((2S)-2-((4R)-4-amino-4-carboxyl-1-oxobutyl)amino-3-(carboxylmethyl)amino-3-oxo-propyl)dithio-propanoic acid" EXACT RESID-systematic []
-synonym: "cysteinyl glutathione" EXACT RESID-alternate []
-synonym: "Glutathionation" EXACT DeltaMass-label []
-synonym: "Glutathione" RELATED PSI-MS-label []
-synonym: "glutathione disulfide" RELATED Unimod-description []
-synonym: "glutathionec" EXACT OMSSA-label []
-synonym: "L-cysteine glutathione disulfide" EXACT RESID-name []
-synonym: "L-gamma-glutamyl-L-cysteinyl-glycine (2-1')-disulfide with L-cysteine" EXACT RESID-alternate []
-synonym: "MOD_RES S-glutathionyl cysteine" EXACT UniProt-feature []
-synonym: "N-(N-gamma-glutamyl-cystinyl)-glycine" EXACT RESID-alternate []
-synonym: "SGltCys" EXACT PSI-MOD-label []
-property_value: DiffAvg "305.30" xsd:float
-property_value: DiffFormula "C 10 H 15 N 3 O 6 S 1" xsd:string
-property_value: DiffMono "305.068156" xsd:float
-property_value: Formula "C 13 H 20 N 4 O 7 S 2" xsd:string
-property_value: MassAvg "408.44" xsd:float
-property_value: MassMono "408.077341" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:55
-xref: uniprot.ptm:PTM-0311
-is_a: MOD:00905
-is_a: MOD:01862
-relationship: contains MOD:02026
-
-[Term]
-id: MOD:00235
-name: S-nitrosyl-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-nitrosyl-L-cysteine." [PubMed:10442087, PubMed:11562475, PubMed:15688001, PubMed:8626764, PubMed:8637569, RESID:AA0230, Unimod:275]
-subset: PSI-MOD-slim
-synonym: "(2R)-2-amino-3-nitrososulfanyl-propanoic acid" EXACT RESID-systematic []
-synonym: "L-cysteine nitrite ester" EXACT RESID-alternate []
-synonym: "MOD_RES S-nitrosocysteine" EXACT UniProt-feature []
-synonym: "Nitrosyl" RELATED PSI-MS-label []
-synonym: "S-nitrosocysteine" EXACT RESID-alternate []
-synonym: "S-nitrosyl-L-cysteine" EXACT RESID-name []
-synonym: "S-nitrosylation" RELATED Unimod-description []
-synonym: "SNOCys" EXACT PSI-MOD-label []
-property_value: DiffAvg "29.00" xsd:float
-property_value: DiffFormula "C 0 H -1 N 1 O 1 S 0" xsd:string
-property_value: DiffMono "28.990164" xsd:float
-property_value: Formula "C 3 H 4 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "132.14" xsd:float
-property_value: MassMono "131.999348" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:275
-xref: uniprot.ptm:PTM-0280
-is_a: MOD:00905
-is_a: MOD:02077
-
-[Term]
-id: MOD:00236
-name: N4-(ADP-ribosyl)-L-asparagine
-def: "A protein modification that effectively converts an L-asparagine residue to N4-(ADP-ribosyl)-L-asparagine." [PubMed:15842200, PubMed:2498316, RESID:AA0231, Unimod:213#N]
-synonym: "(S)-2-amino-4-([adenosine 5'-(trihydrogen diphosphate) 5'->5'-ester with alpha-D-ribofuranosyl]amino)-4-oxobutanoic acid" EXACT RESID-systematic []
-synonym: "ADP Ribose addition" RELATED Unimod-description []
-synonym: "ADP-Ribosyl" RELATED PSI-MS-label []
-synonym: "MOD_RES ADP-ribosylasparagine" EXACT UniProt-feature []
-synonym: "N4-(ADP-ribosyl)-L-asparagine" EXACT RESID-name []
-synonym: "N4-[alpha-D-ribofuranoside 5'->5'-ester with adenosine 5'-(trihydrogen diphosphate)]-L-asparagine" EXACT RESID-alternate []
-synonym: "N4-alpha-D-ribofuranosyl-L-asparagine 5'->5'-ester with adenosine 5'-(trihydrogen diphosphate)" EXACT RESID-alternate []
-property_value: DiffAvg "541.30" xsd:float
-property_value: DiffFormula "C 15 H 21 N 5 O 13 P 2" xsd:string
-property_value: DiffMono "541.061109" xsd:float
-property_value: Formula "C 19 H 27 N 7 O 15 P 2" xsd:string
-property_value: MassAvg "655.41" xsd:float
-property_value: MassMono "655.104036" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:213
-xref: uniprot.ptm:PTM-0054
-is_a: MOD:00752
-is_a: MOD:00903
-
-[Term]
-id: MOD:00237
-name: L-beta-methylthioaspartic acid
-def: "A protein modification that effectively converts an L-aspartic acid residue to L-beta-methylthioaspartic acid." [DeltaMass:61, OMSSA:13, OMSSA:26, PubMed:15473684, PubMed:8844851, RESID:AA0232, Unimod:39#D, ChEBI:73599]
-subset: PSI-MOD-slim
-synonym: "(2R,3Xi)-2-amino-3-(methylsulfanyl)butanedioic acid" EXACT RESID-systematic []
-synonym: "3-(methylthio)-L-aspartic acid" EXACT RESID-name []
-synonym: "3-carboxy-S-methyl-cysteine" EXACT RESID-alternate []
-synonym: "3-methylthio-aspartic acid" EXACT RESID-alternate []
-synonym: "3MeSAsp" EXACT PSI-MOD-label []
-synonym: "beta-Methylthio-aspartic acid" EXACT DeltaMass-label []
-synonym: "beta-methylthio-aspartic acid" EXACT RESID-alternate []
-synonym: "Beta-methylthiolation" RELATED Unimod-description []
-synonym: "bmethylthiold" EXACT OMSSA-label []
-synonym: "Methylthio" RELATED Unimod-interim []
-synonym: "methythiold" EXACT OMSSA-label []
-synonym: "MOD_RES 3-methylthioaspartic acid" EXACT UniProt-feature []
-property_value: DiffAvg "46.09" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0 S 1" xsd:string
-property_value: DiffMono "45.987721" xsd:float
-property_value: Formula "C 5 H 7 N 1 O 3 S 1" xsd:string
-property_value: MassAvg "161.18" xsd:float
-property_value: MassMono "161.014664" xsd:float
-property_value: Origin "D" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:39
-xref: uniprot.ptm:PTM-0032
-is_a: MOD:00904
-is_a: MOD:01153
-
-[Term]
-id: MOD:00238
-name: 5'-(N6-L-lysine)-L-topaquinone
-def: "A protein modification that effectively cross-links an L-lysine residue and an L-tyrosine residue by a carbon-nitrogen bond to form 5'-(N6-L-lysine)-L-topaquinone." [PubMed:8688089, RESID:AA0233]
-comment: Cross-link 2; secondary to RESID:AA0147.
-synonym: "1-[(S)-5-amino-5-carboxypentyl]amino-2-[(S)-2-amino-2-carboxyethyl]-2,6-cyclohexadien-4,5-dione" EXACT RESID-systematic []
-synonym: "2'-(L-lys-N6-yl)-L-4',5'-topaquinone" EXACT RESID-name []
-synonym: "2'-(L-lysine)-L-tyrosyl-4',5'-quinone" EXACT RESID-alternate []
-synonym: "CROSSLNK Lysine tyrosylquinone (Lys-Tyr)" EXACT UniProt-feature []
-synonym: "CROSSLNK Lysine tyrosylquinone (Tyr-Lys)" EXACT UniProt-feature []
-synonym: "LTQ" EXACT RESID-alternate []
-synonym: "lysyl oxidase cofactor" EXACT RESID-alternate []
-property_value: DiffAvg "11.97" xsd:float
-property_value: DiffFormula "C 0 H -4 N 0 O 1" xsd:string
-property_value: DiffMono "11.963614" xsd:float
-property_value: Formula "C 15 H 17 N 3 O 4" xsd:string
-property_value: MassAvg "303.32" xsd:float
-property_value: MassMono "303.121906" xsd:float
-property_value: Origin "K, Y" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0171
-is_a: MOD:00692
-is_a: MOD:02051
-is_a: MOD:02058
-
-[Term]
-id: MOD:00239
-name: S-methyl-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-methyl-L-cysteine." [PubMed:10660523, PubMed:11875433, PubMed:1339288, RESID:AA0234, Unimod:34#C]
-subset: PSI-MOD-slim
-synonym: "(R)-2-amino-3-(methylsulfanyl)propanoic acid" EXACT RESID-systematic []
-synonym: "ACT_SITE S-methylcysteine intermediate" EXACT UniProt-feature []
-synonym: "L-3-(methylthio)alanine" EXACT RESID-alternate []
-synonym: "Methyl" RELATED PSI-MS-label []
-synonym: "Methylation" RELATED Unimod-description []
-synonym: "MOD_RES S-methylcysteine" EXACT UniProt-feature []
-synonym: "S-methyl-L-cysteine" EXACT RESID-name []
-synonym: "S-methylated L-cysteine" EXACT PSI-MOD-alternate []
-synonym: "SMeCys" EXACT PSI-MOD-label []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 4 H 7 N 1 O 1 S 1" xsd:string
-property_value: MassAvg "117.17" xsd:float
-property_value: MassMono "117.024835" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:34
-xref: uniprot.ptm:PTM-0636
-is_a: MOD:00654
-is_a: MOD:01682
-
-[Term]
-id: MOD:00240
-name: 4-hydroxy-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to 4-hydroxy-L-lysine." [PubMed:4005040, RESID:AA0235, ChEBI:141495]
-comment: This modification was not structurally confirmed. Later 5-hydroxy-L-lysine was found at a homologous position in the same protein from closely related species. This is a deprecated entry in RESID. It probably does not occur naturally [JSG].
-synonym: "(2S,4R)-2,6-diamino-4-hydroxyhexanoic acid" EXACT RESID-systematic []
-synonym: "4-hydroxy-L-lysine" EXACT RESID-name []
-synonym: "4-hydroxylated L-lysine" EXACT PSI-MOD-alternate []
-synonym: "4HyLys" EXACT PSI-MOD-label []
-synonym: "alpha,epsilon-diamino-gamma-hydroxycaproic acid" EXACT RESID-alternate []
-synonym: "L-threo-gamma-hydroxylysine" EXACT RESID-alternate []
-synonym: "MOD_RES 4-hydroxylysine" EXACT UniProt-feature []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 6 H 12 N 2 O 2" xsd:string
-property_value: MassAvg "144.17" xsd:float
-property_value: MassMono "144.089878" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: uniprot.ptm:PTM-0664
-is_a: MOD:01047
-
-[Term]
-id: MOD:00241
-name: N4-hydroxymethyl-L-asparagine
-def: "A protein modification that effectively converts an L-asparagine residue to N4-hydroxymethyl-L-asparagine." [RESID:AA0236, Unimod:414]
-comment: N4-methyl-L-asparagine, see MOD:0079, was found at a homologous position of the same protein in a closely related species. Since the peptide containing this modification was obtained by enzymatic cleavage, not cyanogen bromide cleavage, it could have experienced oxidation of the following methionine residue, leading to the erroneous attribution of a mass of 29 for the modification rather than 14. comment: This is a deprecated entry in RESID. It probably does not occur naturally [JSG].
-synonym: "(2S)-2-amino-4-[(hydroxymethyl)amino]-4-oxobutanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-N4-hydroxymethylbutanediamic acid" EXACT RESID-alternate []
-synonym: "beta-hydroxymethylasparagine" EXACT RESID-alternate []
-synonym: "Hydroxymethyl" RELATED PSI-MS-label []
-synonym: "hydroxymethyl" RELATED Unimod-description []
-synonym: "N(gamma)-hydroxymethylasparagine" EXACT RESID-alternate []
-synonym: "N4-hydroxymethyl-L-asparagine" EXACT RESID-name []
-synonym: "N4-hydroxymethylasparagine" EXACT RESID-alternate []
-property_value: DiffAvg "30.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 1" xsd:string
-property_value: DiffMono "30.010565" xsd:float
-property_value: Formula "C 5 H 8 N 2 O 3" xsd:string
-property_value: MassAvg "144.13" xsd:float
-property_value: MassMono "144.053492" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:414
-is_a: MOD:00903
-
-[Term]
-id: MOD:00242
-name: O-(ADP-ribosyl)-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O-(ADP-ribosyl)-L-serine." [PubMed:15842200, PubMed:3141412, RESID:AA0237, Unimod:213#S]
-subset: PSI-MOD-slim
-synonym: "(S)-2-amino-3-([adenosine 5'-(trihydrogen diphosphate) 5'->5'-ester with alpha-D-ribofuranosyl]oxy)-propanoic acid" EXACT RESID-systematic []
-synonym: "ADP Ribose addition" RELATED Unimod-description []
-synonym: "ADP-Ribosyl" RELATED PSI-MS-label []
-synonym: "MOD_RES ADP-ribosylserine" EXACT UniProt-feature []
-synonym: "O-(ADP-ribosyl)-L-serine" EXACT RESID-name []
-synonym: "O3-(ADP-ribosyl)-L-serine" EXACT RESID-alternate []
-synonym: "O3-[alpha-D-ribofuranoside 5'->5'-ester with adenosine 5'-(trihydrogen diphosphate)]-L-serine" EXACT RESID-alternate []
-synonym: "O3-alpha-D-ribofuranosyl-L-serine 5'->5'-ester with adenosine 5'-(trihydrogen diphosphate)" EXACT RESID-alternate []
-synonym: "OADPRibSer" EXACT PSI-MOD-label []
-property_value: DiffAvg "541.30" xsd:float
-property_value: DiffFormula "C 15 H 21 N 5 O 13 P 2" xsd:string
-property_value: DiffMono "541.061109" xsd:float
-property_value: Formula "C 18 H 26 N 6 O 15 P 2" xsd:string
-property_value: MassAvg "628.38" xsd:float
-property_value: MassMono "628.093137" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:213
-xref: uniprot.ptm:PTM-0056
-is_a: MOD:00752
-is_a: MOD:00916
-
-[Term]
-id: MOD:00243
-name: L-cysteine oxazole-4-carboxylic acid
-def: "A protein modification that effectively crosslinks an L-cysteine residue and an L-serine residue to form L-cysteine oxazole-4-carboxylic acid." [PubMed:8183941, PubMed:8895467, RESID:AA0238]
-comment: Cross-link 2.
-synonym: "2-(1-azanyl-2-sulfanylethyl)-4-oxazolecarboxylic acid" EXACT RESID-alternate []
-synonym: "2-[(1R)-1-amino-2-sulfanylethyl]-1,3-oxazole-4-carboxylic acid" EXACT RESID-systematic []
-synonym: "CROSSLNK Oxazole-4-carboxylic acid (Cys-Ser)" EXACT UniProt-feature []
-synonym: "L-cysteine oxazole-4-carboxylic acid" EXACT RESID-name []
-property_value: DiffAvg "-20.03" xsd:float
-property_value: DiffFormula "C 0 H -4 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-20.026215" xsd:float
-property_value: Formula "C 6 H 6 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "170.19" xsd:float
-property_value: MassMono "170.014998" xsd:float
-property_value: Origin "C, S" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0376
-is_a: MOD:02044
-is_a: MOD:01421
-is_a: MOD:02082
-
-[Term]
-id: MOD:00244
-name: L-cysteine oxazoline-4-carboxylic acid
-def: "A protein modification that effectively crosslinks an L-cysteine residue and an L-serine residue to form L-cysteine oxazoline-4-carboxylic acid." [PubMed:1880060, RESID:AA0239]
-comment: Cross-link 2.
-synonym: "(4S)-2-[(1R)-1-amino-2-sulfanylethyl]-4,5-dihydro-1,3-oxazole-4-carboxylic acid" EXACT RESID-systematic []
-synonym: "2-[1-azanyl-2-sulfanylethyl]-4,5-dihydro-1,3-oxazole-4-carboxylic acid" EXACT RESID-alternate []
-synonym: "CROSSLNK Oxazoline-4-carboxylic acid (Cys-Ser)" EXACT UniProt-feature []
-synonym: "L-cysteine oxazoline-4-carboxylic acid" EXACT RESID-name []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 6 H 8 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "172.20" xsd:float
-property_value: MassMono "172.030649" xsd:float
-property_value: Origin "C, S" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0381
-is_a: MOD:02044
-is_a: MOD:01421
-is_a: MOD:00954
-
-[Term]
-id: MOD:00245
-name: glycine oxazole-4-carboxylic acid
-def: "A protein modification that effectively crosslinks a glycine residue and an L-serine residue to form glycine oxazole-4-carboxylic acid." [PubMed:8183941, PubMed:8895467, RESID:AA0240]
-comment: Cross-link 2.
-synonym: "2-aminomethyl-1,3-oxazole-4-carboxylic acid" EXACT RESID-systematic []
-synonym: "2-azanylmethyl-1,3-oxazole-4-carboxylic acid" EXACT RESID-alternate []
-synonym: "CROSSLNK Oxazole-4-carboxylic acid (Gly-Ser)" EXACT UniProt-feature []
-synonym: "glycine oxazole-4-carboxylic acid" EXACT RESID-name []
-property_value: DiffAvg "-20.03" xsd:float
-property_value: DiffFormula "C 0 H -4 N 0 O -1" xsd:string
-property_value: DiffMono "-20.026215" xsd:float
-property_value: Formula "C 5 H 4 N 2 O 2" xsd:string
-property_value: MassAvg "124.10" xsd:float
-property_value: MassMono "124.027277" xsd:float
-property_value: Origin "G, S" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0377
-is_a: MOD:02047
-is_a: MOD:01421
-is_a: MOD:02082
-
-[Term]
-id: MOD:00246
-name: glycine thiazole-4-carboxylic acid
-def: "A protein modification that effectively crosslinks an L-cysteine residue and a glycine residue to form glycine thiazole-4-carboxylic acid." [ChEBI:21276, PubMed:8183941, PubMed:8895467, RESID:AA0241]
-comment: Cross-link 2.
-synonym: "2-(aminomethyl)-1,3-thiazole-4-carboxylic acid" EXACT RESID-systematic []
-synonym: "2-(azanylmethyl)-1,3-thiazole-4-carboxylic acid" EXACT RESID-alternate []
-synonym: "CROSSLNK Thiazole-4-carboxylic acid (Gly-Cys)" EXACT UniProt-feature []
-synonym: "glycine thiazole-4-carboxylic acid" EXACT RESID-name []
-property_value: DiffAvg "-20.03" xsd:float
-property_value: DiffFormula "C 0 H -4 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-20.026215" xsd:float
-property_value: Formula "C 5 H 4 N 2 O 1 S 1" xsd:string
-property_value: MassAvg "140.16" xsd:float
-property_value: MassMono "140.004434" xsd:float
-property_value: Origin "C, G" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0378
-is_a: MOD:02047
-is_a: MOD:01420
-is_a: MOD:02082
-
-[Term]
-id: MOD:00247
-name: L-serine thiazole-4-carboxylic acid
-def: "A protein modification that effectively crosslinks an L-cysteine residue and an L-serine residue to form L-serine thiazole-4-carboxylic acid." [PubMed:8183941, PubMed:8895467, RESID:AA0242]
-comment: Cross-link 2.
-synonym: "2-[(1S)-1-amino-2-hydroxyethyl]-1,3-thiazole-4-carboxylic acid" EXACT RESID-systematic []
-synonym: "2-[1-azanyl-2-hydroxyethyl]-1,3-thiazole-4-carboxylic acid" EXACT RESID-alternate []
-synonym: "CROSSLNK Thiazole-4-carboxylic acid (Ser-Cys)" EXACT UniProt-feature []
-synonym: "L-serine thiazole-4-carboxylic acid" EXACT RESID-name []
-property_value: DiffAvg "-20.03" xsd:float
-property_value: DiffFormula "C 0 H -4 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-20.026215" xsd:float
-property_value: Formula "C 6 H 6 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "170.19" xsd:float
-property_value: MassMono "170.014998" xsd:float
-property_value: Origin "C, S" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0363
-is_a: MOD:02055
-is_a: MOD:01420
-is_a: MOD:02082
-
-[Term]
-id: MOD:00248
-name: L-phenylalanine thiazole-4-carboxylic acid
-def: "A protein modification that effectively crosslinks an L-cysteine residue and an L-phenylalanine residue to form L-phenylalanine thiazole-4-carboxylic acid." [PubMed:1880060, RESID:AA0243]
-comment: Cross-link 2.
-synonym: "2-[(1S)-1-amino-2-phenylethyl]-1,3-thiazole-4-carboxylic acid" EXACT RESID-systematic []
-synonym: "2-[1-azanyl-2-phenylethyl]-1,3-thiazole-4-carboxylic acid" EXACT RESID-alternate []
-synonym: "CROSSLNK Thiazole-4-carboxylic acid (Phe-Cys)" EXACT UniProt-feature []
-synonym: "L-phenylalanine thiazole-4-carboxylic acid" EXACT RESID-name []
-property_value: DiffAvg "-20.03" xsd:float
-property_value: DiffFormula "C 0 H -4 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-20.026215" xsd:float
-property_value: Formula "C 12 H 10 N 2 O 1 S 1" xsd:string
-property_value: MassAvg "230.29" xsd:float
-property_value: MassMono "230.051384" xsd:float
-property_value: Origin "C, F" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0375
-is_a: MOD:02053
-is_a: MOD:01420
-is_a: MOD:02082
-
-[Term]
-id: MOD:00249
-name: L-cysteine thiazole-4-carboxylic acid
-def: "A protein modification that effectively crosslinks two L-cysteine residues to form L-cysteine thiazole-4-carboxylic acid." [PubMed:1880060, RESID:AA0244]
-comment: Cross-link 2.
-synonym: "2-[(1S)-1-amino-2-sulfanylethyl]-1,3-thiazole-4-carboxylic acid" EXACT RESID-systematic []
-synonym: "2-[1-azanyl-2-sulfanylethyl]-1,3-thiazole-4-carboxylic acid" EXACT RESID-alternate []
-synonym: "CROSSLNK Thiazole-4-carboxylic acid (Cys-Cys)" EXACT UniProt-feature []
-synonym: "L-cysteine thiazole-4-carboxylic acid" EXACT RESID-name []
-property_value: DiffAvg "-20.03" xsd:float
-property_value: DiffFormula "C 0 H -4 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-20.026215" xsd:float
-property_value: Formula "C 6 H 6 N 2 O 1 S 2" xsd:string
-property_value: MassAvg "186.25" xsd:float
-property_value: MassMono "185.992155" xsd:float
-property_value: Origin "C, C" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0360
-is_a: MOD:01420
-is_a: MOD:02082
-
-[Term]
-id: MOD:00250
-name: L-lysine thiazole-4-carboxylic acid
-def: "A protein modification that effectively crosslinks an L-cysteine residue and an L-lysine residue to form L-lysine thiazole-4-carboxylic acid." [PubMed:1880060, RESID:AA0245]
-comment: Cross-link 2. Lysine is now thought not to be encoded in the peptide sequence modified to produce GE2270. See RESID:AA0470. This is a deprecated entry in RESID. It probably does not occur naturally [JSG].
-synonym: "2-[(1S)-1,5-diaminopentyl]-1,3-thiazole-4-carboxylic acid" EXACT RESID-systematic []
-synonym: "2-[1,5-bis(azanyl)pentyl]-1,3-thiazole-4-carboxylic acid" EXACT RESID-alternate []
-synonym: "L-lysine thiazole-4-carboxylic acid" EXACT RESID-name []
-property_value: DiffAvg "-20.03" xsd:float
-property_value: DiffFormula "C 0 H -4 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-20.026215" xsd:float
-property_value: Formula "C 9 H 13 N 3 O 1 S 1" xsd:string
-property_value: MassAvg "211.28" xsd:float
-property_value: MassMono "211.077933" xsd:float
-property_value: Origin "C, K" xsd:string
-property_value: Source "hypothetical" xsd:string
-is_a: MOD:02051
-is_a: MOD:01420
-is_a: MOD:02082
-
-[Term]
-id: MOD:00251
-name: O-(phospho-5'-DNA)-L-serine
-def: "A protein modification that effectively crosslinks an L-serine residue and the 5'-end of DNA through a phosphodiester bond to form O-(phospho-5'-DNA)-L-serine." [PubMed:7142163, PubMed:7265205, RESID:AA0246]
-synonym: "(S)-2-amino-3-(5'-deoxyribonucleic acid phosphonoxy)propanoic acid" EXACT RESID-systematic []
-synonym: "ACT_SITE O-(5'-phospho-DNA)-serine intermediate" EXACT UniProt-feature []
-synonym: "MOD_RES O-(5'-phospho-DNA)-serine" EXACT UniProt-feature []
-synonym: "O-(phospho-5'-DNA)-L-serine" EXACT RESID-name []
-synonym: "O3-(phospho-5'-DNA)-L-serine" EXACT RESID-alternate []
-synonym: "O3-L-serine 5'-DNA phosphodiester" EXACT RESID-alternate []
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0226
-is_a: MOD:00750
-is_a: MOD:00916
-
-[Term]
-id: MOD:00252
-name: keratan sulfate D-glucuronosyl-D-galactosyl-D-galactosyl-D-xylosyl-L-threonine
-def: "A protein modification that effectively cross-links an L-threonine residue to the polymer keratan sulfate by a D-glucuronosyl-D-galactosyl-D-galactosyl-D-xylosyl tetrasaccharide." [PubMed:1417734, PubMed:3472204, RESID:AA0247]
-synonym: "keratan sulfate D-glucuronosyl-D-galactosyl-D-galactosyl-D-xylosyl-L-threonine" EXACT RESID-name []
-synonym: "keratosulfate" EXACT RESID-alternate []
-synonym: "poly[beta-1,4-(2-acetamido-2-deoxy-6-sulfate D-glucosyl)-beta-1,3-D-galactosyl]-beta-1,4-D-glucopyranuronosyl-beta-1,3-D-galactosyl-beta-1,3-D-galactosyl-beta-1,4-D-xylosyl-beta-1,3-L-threonine" EXACT RESID-systematic []
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00005
-
-[Term]
-id: MOD:00253
-name: L-selenocysteinyl molybdenum bis(molybdopterin guanine dinucleotide) (Sec)
-def: "A protein modification that effectively converts an L-selenocysteine residue to L-selenocysteinyl molybdenum bis(molybdopterin guanine dinucleotide)." [PubMed:14235557, PubMed:2211698, PubMed:8052647, PubMed:9036855, RESID:AA0248#SEC, Unimod:415]
-property_value: DiffAvg "1572.02" xsd:float
-property_value: DiffFormula "C 40 H 47 Mo 1 N 20 O 26 P 4 S 4 Se 0" xsd:string
-property_value: DiffMono "1572.985775" xsd:float
-property_value: Formula "C 43 H 52 Mo 1 N 21 O 27 P 4 S 4 Se 1" xsd:string
-property_value: MassAvg "1722.07" xsd:float
-property_value: MassMono "1723.939410" xsd:float
-property_value: Origin "U" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:415
-is_a: MOD:00744
-is_a: MOD:01158
-
-[Term]
-id: MOD:00254
-name: O4'-(phospho-5'-RNA)-L-tyrosine
-def: "A protein modification that effectively crosslinks an L-tyrosine residue and the 5'-end of RNA through a phosphodiester to form O4'-(phospho-5'-RNA)-L-tyrosine." [PubMed:1702164, PubMed:209034, PubMed:217003, PubMed:6264310, RESID:AA0249]
-synonym: "(S)-2-amino-3-[4-(5'-ribonucleic acid phosphonoxy)phenyl]propanoic acid" EXACT RESID-systematic []
-synonym: "MOD_RES O-(5'-phospho-RNA)-tyrosine" EXACT UniProt-feature []
-synonym: "O4'-(phospho-5'-RNA)-L-tyrosine" EXACT RESID-name []
-synonym: "O4'-L-tyrosine 5'-RNA phosphodiester" EXACT RESID-alternate []
-property_value: Origin "Y" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0229
-is_a: MOD:00751
-is_a: MOD:00919
-
-[Term]
-id: MOD:00255
-name: 3-(3'-L-histidyl)-L-tyrosine
-def: "A protein modification that effectively cross-links an L-histidine residue and an L-tyrosine residue by a carbon-nitrogen bond to form 3-(3'-L-histidyl)-L-tyrosine." [PubMed:9144772, RESID:AA0250]
-comment: Cross-link 2.
-synonym: "(2S,3R)-2-amino-3-(5-[(2S)-2-amino-2-carboxyethyl]-1H-imidazol-1-yl)-3-(4-hydroxyphenyl)propanoic acid" EXACT RESID-systematic []
-synonym: "3-(3'-L-histidyl)-L-tyrosine" EXACT RESID-name []
-synonym: "3-(N3'-histidyl)tyrosine" EXACT RESID-alternate []
-synonym: "3-(pi-histidyl)tyrosine" EXACT RESID-alternate []
-synonym: "3-(pros-histidyl)tyrosine" EXACT RESID-alternate []
-synonym: "beta-(N(delta)-histidyl)tyrosine" EXACT RESID-alternate []
-synonym: "beta-(N3'-histidyl)tyrosine" EXACT RESID-alternate []
-synonym: "CROSSLNK 3'-histidyl-3-tyrosine (His-Tyr)" EXACT UniProt-feature []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 15 H 14 N 4 O 3" xsd:string
-property_value: MassAvg "298.30" xsd:float
-property_value: MassMono "298.106590" xsd:float
-property_value: Origin "H, Y" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0027
-is_a: MOD:00692
-is_a: MOD:02048
-is_a: MOD:02058
-
-[Term]
-id: MOD:00256
-name: L-methionine sulfone
-def: "A protein modification that dioxygenates an L-methionine residue to L-methionine sulfone." [DeltaMass:205, OMSSA:115, PubMed:12686488, PubMed:7786407, PubMed:7791219, PubMed:9252331, RESID:AA0251, Unimod:425#M]
-comment: DeltaMass gives the formula C 5 H 9 N 3 O 1 S 1 with mass 163
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-4-(methylsulfonyl)butanoic acid" EXACT RESID-systematic []
-synonym: "dihydroxy" RELATED Unimod-description []
-synonym: "Dioxidation" RELATED PSI-MS-label []
-synonym: "L-methionine S,S-dioxide" EXACT RESID-alternate []
-synonym: "L-methionine sulfone" EXACT RESID-name []
-synonym: "MethionylSulphone" EXACT DeltaMass-label []
-synonym: "MetO2" EXACT PSI-MOD-label []
-synonym: "MOD_RES Methionine sulfone" EXACT UniProt-feature []
-synonym: "Oxidation of Methionine (to Sulphone)" EXACT DeltaMass-label []
-synonym: "S,S-dioxymethionine" EXACT RESID-alternate []
-synonym: "suphonem" EXACT OMSSA-label []
-property_value: DiffAvg "32.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 2 S 0" xsd:string
-property_value: DiffMono "31.989829" xsd:float
-property_value: Formula "C 5 H 9 N 1 O 3 S 1" xsd:string
-property_value: MassAvg "163.19" xsd:float
-property_value: MassMono "163.030314" xsd:float
-property_value: Origin "M" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:425
-xref: uniprot.ptm:PTM-0175
-is_a: MOD:00709
-is_a: MOD:01855
-
-[Term]
-id: MOD:00257
-name: dipyrrolylmethanemethyl-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to dipyrrolylmethanemethyl-L-cysteine." [PubMed:3042456, PubMed:3196304, PubMed:3421931, PubMed:8727319, RESID:AA0252, Unimod:416]
-synonym: "(2S)-3-[5-[4-(2-carboxy)ethyl-3-carboxymethyl-1-pyrrol-2-yl]methyl-4-(2-carboxy)ethyl-3-carboxymethyl-1-pyrrol-2-yl]methylthio-2-aminopropanoic acid" EXACT RESID-systematic []
-synonym: "3-[5-(3-acetic acid-4-propanoic acid-1-pyrrol-2-yl)methyl-3-acetic acid-4-propanoic acid-1-pyrrol-2-yl]methylthio-2-aminopropanoic acid" EXACT RESID-alternate []
-synonym: "dipyrrole cofactor" EXACT RESID-alternate []
-synonym: "Dipyrrolylmethanemethyl" RELATED PSI-MS-label []
-synonym: "dipyrrolylmethanemethyl" RELATED Unimod-description []
-synonym: "dipyrrolylmethanemethyl-L-cysteine" EXACT RESID-name []
-synonym: "dipyrrolylmethyl-L-cysteine" EXACT RESID-alternate []
-synonym: "dipyrromethane cofactor" EXACT RESID-alternate []
-synonym: "MOD_RES S-(dipyrrolylmethanemethyl)cysteine" EXACT UniProt-feature []
-synonym: "pyrromethane cofactor" EXACT RESID-alternate []
-property_value: DiffAvg "418.40" xsd:float
-property_value: DiffFormula "C 20 H 22 N 2 O 8 S 0" xsd:string
-property_value: DiffMono "418.137616" xsd:float
-property_value: Formula "C 23 H 27 N 3 O 9 S 1" xsd:string
-property_value: MassAvg "521.54" xsd:float
-property_value: MassMono "521.146800" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:416
-xref: uniprot.ptm:PTM-0421
-is_a: MOD:00905
-
-[Term]
-id: MOD:00258
-name: S-(2-aminovinyl)-3-methyl-D-cysteine
-def: "A protein modification that effectively cross-links an L-cysteine residue and an L-threonine residue by a thioether bond to form S-(2-aminovinyl)-3-methyl-D-cysteine." [PubMed:9119018, RESID:AA0253]
-comment: Cross-link 2.
-synonym: "(2S,3S)-2-amino-3-[((Z)-2-aminoethenyl)sulfanyl]butanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-3-[(2-aminovinyl)sulfanyl]butanoic acid" EXACT RESID-alternate []
-synonym: "CROSSLNK S-(2-aminovinyl)-3-methyl-D-cysteine (Thr-Cys)" EXACT UniProt-feature []
-synonym: "decarboxylated methyllanthionine" EXACT RESID-alternate []
-synonym: "S-(2-aminovinyl)-3-methyl-D-cysteine" EXACT RESID-name []
-property_value: DiffAvg "-64.04" xsd:float
-property_value: DiffFormula "C -1 H -4 N 0 O -3 S 0" xsd:string
-property_value: DiffMono "-64.016044" xsd:float
-property_value: Formula "C 6 H 9 N 2 O 1 S 1" xsd:string
-property_value: MassAvg "157.21" xsd:float
-property_value: MassMono "157.043559" xsd:float
-property_value: Origin "C, T" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0267
-is_a: MOD:00687
-is_a: MOD:02056
-
-[Term]
-id: MOD:00259
-name: O4'-(phospho-5'-DNA)-L-tyrosine
-def: "A protein modification that effectively crosslinks an L-tyrosine residue and the 5'-end of DNA through a phosphodiester bond to form O4'-(phospho-5'-DNA)-L-tyrosine." [PubMed:1861973, PubMed:2940511, PubMed:3684578, RESID:AA0254]
-synonym: "(S)-2-amino-3-[4-(5'-deoxyribonucleic acid phosphonoxy)phenyl]propanoic acid" EXACT RESID-systematic []
-synonym: "ACT_SITE O-(5'-phospho-DNA)-tyrosine intermediate" EXACT UniProt-feature []
-synonym: "MOD_RES O-(5'-phospho-DNA)-tyrosine" EXACT UniProt-feature []
-synonym: "O4'-(phospho-5'-DNA)-L-tyrosine" EXACT RESID-name []
-synonym: "O4'-L-tyrosine 5'-DNA phosphodiester" EXACT RESID-alternate []
-property_value: Origin "Y" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0228
-is_a: MOD:00750
-is_a: MOD:00919
-
-[Term]
-id: MOD:00260
-name: O-(phospho-5'-DNA)-L-threonine
-def: "A protein modification that effectively crosslinks an L-threonine residue and the 5'-end of DNA through a phosphodiester bond to form O-(phospho-5'-DNA)-L-threonine." [PubMed:3081736, RESID:AA0255]
-synonym: "(S)-2-amino-3-(5'-deoxyribonucleic acid phosphonoxy)butanoic acid" EXACT RESID-systematic []
-synonym: "O-(phospho-5'-DNA)-L-threonine" EXACT RESID-name []
-synonym: "O3-(phospho-5'-DNA)-L-threonine" EXACT RESID-alternate []
-synonym: "O3-L-threonine 5'-DNA phosphodiester" EXACT RESID-alternate []
-property_value: DiffAvg "78.97" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 3 P 1" xsd:string
-property_value: DiffMono "78.958505" xsd:float
-property_value: Formula "C 4 H 7 N 1 O 5 P 1" xsd:string
-property_value: MassAvg "180.08" xsd:float
-property_value: MassMono "180.006184" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00750
-is_a: MOD:00917
-
-[Term]
-id: MOD:00261
-name: O4'-(phospho-5'-uridine)-L-tyrosine
-def: "A protein modification that effectively crosslinks an L-tyrosine residue and 5'-phosphouridine through a phosphodiester bond to form O4'-(phospho-5'-uridine)-L-tyrosine." [DeltaMass:0, PubMed:11467524, PubMed:2885322, RESID:AA0256, Unimod:417#Y]
-comment: From DeltaMass: Average Mass: 306.
-subset: PSI-MOD-slim
-synonym: "(S)-2-amino-3-[4-(5'-uridine phosphonoxy)phenyl]propanoic acid" EXACT RESID-systematic []
-synonym: "5'-uridylic-O-tyrosine" EXACT RESID-alternate []
-synonym: "hydrogen 5'-uridylate tyrosine ester" EXACT RESID-alternate []
-synonym: "MOD_RES O-UMP-tyrosine" EXACT UniProt-feature []
-synonym: "O-Uridinylylation (of Tyrosine)" EXACT DeltaMass-label []
-synonym: "O4'-(phospho-5'-uridine)-L-tyrosine" EXACT RESID-name []
-synonym: "O4'-L-tyrosine 5'-uridine phosphodiester" EXACT RESID-alternate []
-synonym: "OUMPTyr" EXACT PSI-MOD-label []
-synonym: "PhosphoUridine" RELATED PSI-MS-label []
-synonym: "uridine phosphodiester" RELATED Unimod-description []
-property_value: DiffAvg "306.17" xsd:float
-property_value: DiffFormula "C 9 H 11 N 2 O 8 P 1" xsd:string
-property_value: DiffMono "306.025302" xsd:float
-property_value: Formula "C 18 H 20 N 3 O 10 P 1" xsd:string
-property_value: MassAvg "469.34" xsd:float
-property_value: MassMono "469.088630" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:417
-xref: uniprot.ptm:PTM-0333
-is_a: MOD:00919
-is_a: MOD:01166
-
-[Term]
-id: MOD:00262
-name: N-(L-glutamyl)-L-tyrosine
-def: "A protein modification that effectively forms a peptide bond between a C-terminal L-glutamic acid residue and a free L-tyrosine." [ChEBI:21477, PubMed:6387372, PubMed:8093886, RESID:AA0257]
-comment: Cross-link 2.
-synonym: "(S,S)-2-(2-aminopentanedio-1-yl)amino-3-(4-hydoxyphenyl)propanoic acid" EXACT RESID-systematic []
-synonym: "L-glutamyl L-tyrosine" EXACT RESID-name []
-synonym: "N-(L-glutamyl)-L-tyrosine" EXACT RESID-alternate []
-synonym: "SITE Involved in polymerization" EXACT UniProt-feature []
-property_value: DiffAvg "-17.01" xsd:float
-property_value: DiffFormula "C 0 H -1 N 0 O -1" xsd:string
-property_value: DiffMono "-17.002740" xsd:float
-property_value: Formula "C 14 H 16 N 2 O 5" xsd:string
-property_value: MassAvg "292.29" xsd:float
-property_value: MassMono "292.105922" xsd:float
-property_value: Origin "E, Y" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-is_a: MOD:02045
-is_a: MOD:00919
-
-[Term]
-id: MOD:00263
-name: S-phycoviolobilin-L-cysteine
-def: "A protein modification that effectively results from forming an adduct between a cysteine residue and the tetrapyrrole compound phycoviolobilin." [PubMed:2106585, PubMed:3208761, RESID:AA0258, Unimod:387]
-synonym: "(4S)-3-[(1R)-1-(((2R)-2-amino-2-carboxy)ethylsulfanyl)ethyl]-8,12-bis(2-carboxyethyl)-18-ethyl-4,5-dihydro-2,7,13,17-tetramethyl-(21H,22H,24H)-biladiene-bc-1,19-dione" EXACT RESID-systematic []
-synonym: "BINDING Phycoviolobilin chromophore (covalent; via 1 link)" EXACT UniProt-feature []
-synonym: "cryptobiliviolin" EXACT RESID-alternate []
-synonym: "cryptoviolin" EXACT RESID-alternate []
-synonym: "cryptoviolobilin" EXACT RESID-alternate []
-synonym: "PBV" EXACT RESID-alternate []
-synonym: "Phycocyanobilin" RELATED PSI-MS-label []
-synonym: "phycocyanobilin" RELATED Unimod-description []
-synonym: "PVB" EXACT RESID-alternate []
-synonym: "PXB" EXACT RESID-alternate []
-synonym: "S-phycobiliviolin-L-cysteine" EXACT RESID-alternate []
-synonym: "S-phycoviolobilin-L-cysteine" EXACT RESID-name []
-property_value: DiffAvg "586.69" xsd:float
-property_value: DiffFormula "C 33 H 38 N 4 O 6 S 0" xsd:string
-property_value: DiffMono "586.279135" xsd:float
-property_value: Formula "C 36 H 43 N 5 O 7 S 1" xsd:string
-property_value: MassAvg "689.83" xsd:float
-property_value: MassMono "689.288320" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:387
-is_a: MOD:00700
-is_a: MOD:00905
-
-[Term]
-id: MOD:00264
-name: phycoerythrobilin-bis-L-cysteine
-def: "A protein modification that effectively results from forming an adduct between two cysteine residues and the tetrapyrrole compound phycoerythrobilin." [PubMed:3208761, PubMed:3838747, RESID:AA0259]
-comment: Cross-link 2.
-synonym: "(2S,3R,16R)-3,18-bis-[(R)-1-(((2R)-2-amino-2-carboxy)ethylsulfanyl)ethyl]-8,12-bis(2-carboxyethyl)-2,7,13,17-tetramethyl-2,3,15,16-tetrahydrobilin-1,19(21H,22H,24H)-dione" EXACT RESID-systematic []
-synonym: "3,18-bis-[1-((2-amino-2-carboxy)ethylsulfanyl)ethyl]-2,3,15,16-tetrahydro-2,7,13,17-tetramethyl-1,19-dioxo-(21H,22H,24H)-biladiene-ab-8,12-dipropanoic acid" EXACT RESID-alternate []
-synonym: "BINDING Phycoerythrobilin chromophore (covalent; via 2 links)" EXACT UniProt-feature []
-synonym: "PEB" EXACT RESID-alternate []
-synonym: "phycoerythrobilin biscysteine adduct" EXACT RESID-alternate []
-synonym: "phycoerythrobilin-bis-L-cysteine" EXACT RESID-name []
-property_value: DiffAvg "586.69" xsd:float
-property_value: DiffFormula "C 33 H 38 N 4 O 6 S 0" xsd:string
-property_value: DiffMono "586.279135" xsd:float
-property_value: Formula "C 39 H 48 N 6 O 8 S 2" xsd:string
-property_value: MassAvg "792.97" xsd:float
-property_value: MassMono "792.297505" xsd:float
-property_value: Origin "C, C" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00700
-is_a: MOD:02044
-
-[Term]
-id: MOD:00265
-name: phycourobilin-bis-L-cysteine
-def: "A protein modification that effectively results from forming an adduct between two cysteine residues and the tetrapyrrole compound phycourobilin." [PubMed:3208761, PubMed:3838665, PubMed:3838747, PubMed:8876649, RESID:AA0260]
-comment: Cross-link 2.
-synonym: "3,18-bis(1-[(R)-2-amino-2-carboxyethyl]sulfanylethyl)-2,7,13,17-tetramethyl-1,19-dioxo-4,5,15,16-tetrahydro-(21H,22H,24H)-bilene-b-8,12-dipropanoic acid" EXACT RESID-alternate []
-synonym: "3,18-bis(1-[(R)-2-amino-2-carboxyethyl]sulfanylethyl)-8,12-bis(2-carboxyethyl)-2,7,13,17-tetramethyl-4,5,15,16-tetrahydro-(21H,22H,24H)-bilene-b-1,19(4H,16H)-dione" EXACT RESID-systematic []
-synonym: "BINDING Phycourobilin chromophore (covalent; via 2 links)" EXACT UniProt-feature []
-synonym: "phycourobilin biscysteine adduct" EXACT RESID-alternate []
-synonym: "phycourobilin-bis-L-cysteine" EXACT RESID-name []
-synonym: "PUB" EXACT RESID-alternate []
-property_value: DiffAvg "586.69" xsd:float
-property_value: DiffFormula "C 33 H 38 N 4 O 6 S 0" xsd:string
-property_value: DiffMono "586.279135" xsd:float
-property_value: Formula "C 39 H 48 N 6 O 8 S 2" xsd:string
-property_value: MassAvg "792.97" xsd:float
-property_value: MassMono "792.297505" xsd:float
-property_value: Origin "C, C" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00700
-is_a: MOD:02044
-
-[Term]
-id: MOD:00266
-name: N-L-glutamyl-poly-L-glutamic acid
-def: "A protein modification that effectively forms a peptide bond between a C-terminal L-glutamic acid residue and one or more free L-glutamic acid molecules to form N-(L-glutamyl)-poly-L-glutamic acid." [PubMed:2570347, PubMed:328274, RESID:AA0261]
-property_value: Origin "E" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-is_a: MOD:00906
-
-[Term]
-id: MOD:00267
-name: L-cysteine sulfinic acid
-def: "A protein modification that effectively dioxygenates an L-cysteine residue to L-cysteine sulfinic acid." [ChEBI:16345, OMSSA:162, PubMed:12686488, PubMed:9252331, PubMed:9586994, RESID:AA0262, Unimod:425#C]
-comment: \"Hyun Ae Woo, et. al., Science 300 (5619), 653-656\"
-subset: PSI-MOD-slim
-synonym: "(2R)-2-amino-3-sulfinopropanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-2-carboxyethanesulfinic acid" EXACT RESID-alternate []
-synonym: "2-amino-3-(dioxido-lambda(6)-sulfanyl)propanoic acid [tautomer]" EXACT RESID-alternate []
-synonym: "2-amino-3-sulfonylpropanoic acid [tautomer]" EXACT RESID-alternate []
-synonym: "3-sulfinoalanine" EXACT RESID-alternate []
-synonym: "3-sulphinoalanine" EXACT RESID-alternate []
-synonym: "CysO2H" EXACT PSI-MOD-label []
-synonym: "cysteine sulphinic acid" EXACT RESID-alternate []
-synonym: "cysteine-S,S-dioxide [tautomer]" EXACT RESID-alternate []
-synonym: "dihydroxy" RELATED Unimod-description []
-synonym: "Dioxidation" RELATED PSI-MS-label []
-synonym: "L-cysteine sulfinic acid" EXACT RESID-name []
-synonym: "MOD_RES Cysteine sulfinic acid (-SO2H)" EXACT UniProt-feature []
-synonym: "S-cysteinesulfinic acid" EXACT RESID-alternate []
-synonym: "S-sulfinocysteine" EXACT RESID-alternate []
-synonym: "sulfinicacid" EXACT OMSSA-label []
-property_value: DiffAvg "32.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 2 S 0" xsd:string
-property_value: DiffMono "31.989829" xsd:float
-property_value: Formula "C 3 H 5 N 1 O 3 S 1" xsd:string
-property_value: MassAvg "135.14" xsd:float
-property_value: MassMono "134.999014" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:425
-xref: uniprot.ptm:PTM-0108
-is_a: MOD:00708
-is_a: MOD:01855
-
-[Term]
-id: MOD:00268
-name: L-3',4',5'-trihydroxyphenylalanine
-def: "A protein modification that effectively converts an L-tyrosine residue to L-3',4',5'-trihydroxyphenylalanine." [DeltaMass:0, PubMed:12686488, PubMed:12771378, PubMed:8554314, PubMed:9252331, PubMed:9434739, RESID:AA0263, Unimod:425#Y, ChEBI:141811]
-comment: From DeltaMass: Average Mass: 32
-synonym: "(S)-2-amino-3-(3,4,5-trihydroxyphenyl)propanoic acid" EXACT RESID-systematic []
-synonym: "3,4,6-Trihydroxy-Phenylalanine (from Tyrosine) (TOPA)" EXACT DeltaMass-label []
-synonym: "35Hy2Tyr" EXACT PSI-MOD-label []
-synonym: "dihydroxy" RELATED Unimod-description []
-synonym: "Dioxidation" RELATED PSI-MS-label []
-synonym: "L-3',4',5'-trihydroxyphenylalanine" EXACT RESID-name []
-synonym: "L-3,4,5-TOPA" EXACT RESID-alternate []
-synonym: "MOD_RES 3',4',5'-trihydroxyphenylalanine" EXACT UniProt-feature []
-property_value: DiffAvg "32.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 2" xsd:string
-property_value: DiffMono "31.989829" xsd:float
-property_value: Formula "C 9 H 9 N 1 O 4" xsd:string
-property_value: MassAvg "195.17" xsd:float
-property_value: MassMono "195.053158" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:425
-xref: uniprot.ptm:PTM-0667
-is_a: MOD:00428
-is_a: MOD:00707
-
-[Term]
-id: MOD:00269
-name: O-(sn-1-glycerophosphoryl)-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O-(sn-1-glycerophosphoryl)-L-serine." [PubMed:8645220, RESID:AA0264, Unimod:419#S]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-[(2Xi)-2,3-dihydroxypropyl]phosphonoxypropanoic acid" EXACT RESID-systematic []
-synonym: "alpha-glycerophosphoryl serine" EXACT RESID-alternate []
-synonym: "Glycerophospho" RELATED PSI-MS-label []
-synonym: "glycerophospho" RELATED Unimod-description []
-synonym: "glycerophosphoserine" EXACT RESID-alternate []
-synonym: "MOD_RES O-(sn-1-glycerophosphoryl)serine" EXACT UniProt-feature []
-synonym: "O-(sn-1-glycerophosphoryl)-L-serine" EXACT RESID-name []
-synonym: "O3-(sn-1-glycerophosphoryl)-L-serine" EXACT RESID-alternate []
-synonym: "O3-2,3-dihydroxypropyl hydrogen phosphate-L-serine ester" EXACT RESID-alternate []
-synonym: "O3-L-serine glyceryl-1-phosphodiester" EXACT RESID-alternate []
-property_value: DiffAvg "154.06" xsd:float
-property_value: DiffFormula "C 3 H 7 N 0 O 5 P 1" xsd:string
-property_value: DiffMono "154.003110" xsd:float
-property_value: Formula "C 6 H 12 N 1 O 7 P 1" xsd:string
-property_value: MassAvg "241.14" xsd:float
-property_value: MassMono "241.035138" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:419
-xref: uniprot.ptm:PTM-0230
-is_a: MOD:00916
-
-[Term]
-id: MOD:00270
-name: 1-thioglycine (internal)
-def: "A protein modification that effectively converts a glycine residue to an internal 1-thioglycine." [PubMed:11463785, PubMed:9367957, RESID:AA0265#INT]
-comment: This modification occurs naturally in two forms. At an interior peptide location it exists as aminoethanethionic acid (or aminoethanethioic O-acid). At the carboxyl-terminal it exists as aminoethanethiolic acid (or aminoethanethioic S-acid).
-subset: PSI-MOD-slim
-synonym: "1-thioglycine" EXACT RESID-name []
-synonym: "2-amino-1-sulfanylethanone" EXACT RESID-alternate []
-synonym: "aminoethanethioic acid" EXACT RESID-systematic []
-synonym: "aminoethanethioic O-acid" EXACT RESID-alternate []
-synonym: "aminoethanethionic acid" EXACT RESID-alternate []
-synonym: "aminothioacetic acid" EXACT RESID-alternate []
-synonym: "Carboxy->Thiocarboxy" RELATED PSI-MS-label []
-synonym: "MOD_RES 1-thioglycine" EXACT UniProt-feature []
-synonym: "S(O)Gly" EXACT PSI-MOD-label []
-synonym: "thiocarboxylic acid" RELATED Unimod-description []
-property_value: DiffAvg "16.06" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O -1 S 1" xsd:string
-property_value: DiffMono "15.977156" xsd:float
-property_value: Formula "C 2 H 3 N 1 S 1" xsd:string
-property_value: MassAvg "73.11" xsd:float
-property_value: MassMono "72.998620" xsd:float
-property_value: Origin "G" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0004
-is_a: MOD:01625
-
-[Term]
-id: MOD:00271
-name: heme P460-bis-L-cysteine-L-tyrosine
-def: "A protein modification that effectively results from forming an adduct between two cysteine residues, the C-3' of a tyrosine residue, and the porphyrin compound heme b, (7,12-diethenyl-3,8,13,17-tetramethylporphyrin-2,18-dipropanoato)iron." [PubMed:8325841, PubMed:9095195, RESID:AA0266]
-comment: Cross-link 3.
-synonym: "(10S,11S)-[7,12-bis((S)-1-[((R)-2-amino-2-carboxy)ethylsulfanyl]ethyl)-10-(2-hydroxy-5-[(S)-2-amino-2-carboxy]ethylphenyl)-3,8,13,17-tetramethyl-21H,23H-10,11-dihydroporphine-2,18-bis(2-carboxyethyl)-N21,N22,N23,N24]-ferrate" EXACT RESID-systematic []
-synonym: "BINDING Heme (covalent; via 3 links)" EXACT UniProt-feature []
-synonym: "bis(S-cysteinyl)-(tyros-3'-yl)-heme" EXACT RESID-alternate []
-synonym: "heme P460-bis-L-cysteine-L-tyrosine" EXACT RESID-name []
-property_value: DiffAvg "614.48" xsd:float
-property_value: DiffFormula "C 34 Fe 1 H 30 N 4 O 4 S 0" xsd:string
-property_value: DiffMono "614.161643" xsd:float
-property_value: Formula "C 49 Fe 1 H 49 N 7 O 8 S 2" xsd:string
-property_value: MassAvg "983.94" xsd:float
-property_value: MassMono "983.243341" xsd:float
-property_value: Origin "C, C, Y" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00699
-is_a: MOD:02067
-is_a: MOD:02075
-
-[Term]
-id: MOD:00272
-name: O-(phospho-5'-adenosine)-L-threonine
-def: "A protein modification that effectively crosslinks an L-threonine residue and 5'-phosphoadenosine through a phosphodiester bond to form O-(phospho-5'-adenosine)-L-threonine." [PubMed:2989287, PubMed:8917428, RESID:AA0267, Unimod:405#T]
-subset: PSI-MOD-slim
-synonym: "(2S,3R)-2-amino-3-(5'-adenosine phosphonoxy)butanoic acid" EXACT RESID-systematic []
-synonym: "5'-adenylic-O3-L-threonine" EXACT RESID-alternate []
-synonym: "ACT_SITE O-AMP-threonine intermediate" EXACT UniProt-feature []
-synonym: "AMP binding site" RELATED Unimod-description []
-synonym: "beta-5'-adenylic-L-threonine" EXACT RESID-alternate []
-synonym: "L-threonine monoanhydride with 5'-adenylic acid" EXACT RESID-alternate []
-synonym: "MOD_RES O-AMP-threonine" EXACT UniProt-feature []
-synonym: "O(gamma)-5'-adenylic-L-threonine" EXACT RESID-alternate []
-synonym: "O-(phospho-5'-adenosine)-L-threonine" EXACT RESID-name []
-synonym: "O3-(phospho-5'-adenosine)-L-threonine" EXACT RESID-alternate []
-synonym: "O3-L-threonine 5'-adenosine phosphodiester" EXACT RESID-alternate []
-synonym: "Phosphoadenosine" RELATED PSI-MS-label []
-property_value: DiffAvg "329.21" xsd:float
-property_value: DiffFormula "C 10 H 12 N 5 O 6 P 1" xsd:string
-property_value: DiffMono "329.052520" xsd:float
-property_value: Formula "C 14 H 19 N 6 O 8 P 1" xsd:string
-property_value: MassAvg "430.31" xsd:float
-property_value: MassMono "430.100198" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:405
-xref: uniprot.ptm:PTM-0393
-is_a: MOD:00917
-is_a: MOD:01165
-
-[Term]
-id: MOD:00273
-name: tris-L-cysteinyl L-cysteine persulfido bis-L-glutamato L-histidino tetrairon disulfide trioxide
-def: "A protein modification that effectively converts four L-cysteine residues, two L-glutamic acid residues, an L-histidine residue and a four-iron three-sulfur three-oxygen cluster to tris-L-cysteinyl L-cysteine persulfido bis-L-glutamato L-histidino tetrairon disulfide trioxide." [PubMed:12764602, RESID:AA0268]
-comment: Cross-link 7; secondary to RESID:AA0269.
-synonym: "4Fe-2S-3O cluster" EXACT RESID-alternate []
-synonym: "hybrid four iron cluster 2" EXACT RESID-alternate []
-synonym: "METAL Iron-oxo-sulfur (4Fe-2O-2S)" EXACT UniProt-feature []
-synonym: "METAL Iron-oxo-sulfur (4Fe-2O-2S); via persulfide group" EXACT UniProt-feature []
-synonym: "METAL Iron-oxo-sulfur (4Fe-2O-2S); via tele nitrogen" EXACT UniProt-feature []
-synonym: "mu-1:2kappaO-oxido-mu-1:3kappaO-oxido-mu-2:4kappaO-oxido-mu-3:4kappaS-sulfido-mu3-2:3:4kappaS-sulfido-S-cysteinyl-N1'-histidino-O5-glutamato 1-iron-S5-cysteine persulfido-O5-glutamato 2-iron-3,4-bis-(S-cysteinyl iron)" EXACT RESID-systematic []
-synonym: "prismane iron-sulfur cofactor" RELATED RESID-misnomer []
-synonym: "tris-L-cysteinyl L-cysteine persulfido bis-L-glutamato L-histidino tetrairon disulfide trioxide" EXACT RESID-name []
-property_value: DiffAvg "360.50" xsd:float
-property_value: DiffFormula "C 0 Fe 4 H -7 N 0 O 3 S 3" xsd:string
-property_value: DiffMono "360.585932" xsd:float
-property_value: Formula "C 28 Fe 4 H 34 N 9 O 14 S 7" xsd:string
-property_value: MassAvg "1168.43" xsd:float
-property_value: MassMono "1167.766769" xsd:float
-property_value: Origin "C, C, C, C, E, E, H" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00739
-is_a: MOD:02067
-is_a: MOD:02068
-is_a: MOD:02070
-
-[Term]
-id: MOD:00274
-name: L-cysteine persulfide
-def: "A protein modification that effectively replaces the hydrogen atom of a cysteine sulfanyl group with a sulfanyl group, forming a disulfanyl group, and converting an L-cysteine residue to L-cysteine persulfide." [ChEBI:28839, PubMed:15096637, PubMed:4276457, PubMed:8161529, RESID:AA0269, Unimod:421]
-subset: PSI-MOD-slim
-synonym: "(R)-2-amino-3-disulfanylpropanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-3-disulfanylpropanoic acid" EXACT RESID-alternate []
-synonym: "2-amino-3-hydrodisulfidopropanoic acid" EXACT RESID-alternate []
-synonym: "2-amino-3-hydropersulfidopropanoic acid" EXACT RESID-alternate []
-synonym: "2-amino-3-persulfhydrylpropanoic acid" EXACT RESID-alternate []
-synonym: "3-(thiosulfeno)-alanine" EXACT RESID-alternate []
-synonym: "3-disulfanylalanine" EXACT RESID-alternate []
-synonym: "ACT_SITE Cysteine persulfide intermediate" EXACT UniProt-feature []
-synonym: "L-cysteine persulfide" EXACT RESID-name []
-synonym: "MOD_RES Cysteine persulfide" EXACT UniProt-feature []
-synonym: "persulfide" RELATED Unimod-description []
-synonym: "S-mercaptocysteine" EXACT RESID-alternate []
-synonym: "S-sulfanylcysteine" EXACT RESID-alternate []
-synonym: "Sulfide" RELATED PSI-MS-label []
-synonym: "thiocysteine" EXACT RESID-alternate []
-property_value: DiffAvg "32.06" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0 S 1" xsd:string
-property_value: DiffMono "31.972071" xsd:float
-property_value: Formula "C 3 H 5 N 1 O 1 S 2" xsd:string
-property_value: MassAvg "135.20" xsd:float
-property_value: MassMono "134.981256" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:421
-xref: uniprot.ptm:PTM-0106
-is_a: MOD:00905
-is_a: MOD:01886
-
-[Term]
-id: MOD:00275
-name: 3'-(1'-L-histidyl)-L-tyrosine
-def: "A protein modification that effectively cross-links an L-histidine residue and an L-tyrosine residue by a carbon-nitrogen bond to form 3'-(1'-L-histidyl)-L-tyrosine." [ChEBI:19837, PubMed:10338009, RESID:AA0270]
-comment: Cross-link 2.
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-[1-(5-[(2S)-2-amino-2-carboxyethyl]-2-hydroxyphenyl)-1H-imidazol-4-yl]propanoic acid" EXACT RESID-systematic []
-synonym: "3'-(1'-L-histidyl)-L-tyrosine" EXACT RESID-name []
-synonym: "3'-(N(epsilon)-histidyl)tyrosine" EXACT RESID-alternate []
-synonym: "3'-(N1'-histidyl)tyrosine" EXACT RESID-alternate []
-synonym: "3'-(tau-histidyl)tyrosine" EXACT RESID-alternate []
-synonym: "3'-(tele-histidyl)tyrosine" EXACT RESID-alternate []
-synonym: "CROSSLNK 1'-histidyl-3'-tyrosine (His-Tyr)" EXACT UniProt-feature []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 15 H 14 N 4 O 3" xsd:string
-property_value: MassAvg "298.30" xsd:float
-property_value: MassMono "298.106590" xsd:float
-property_value: Origin "H, Y" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0003
-is_a: MOD:00692
-is_a: MOD:02048
-is_a: MOD:02058
-
-[Term]
-id: MOD:00276
-name: heme P460-bis-L-cysteine-L-lysine
-def: "A protein modification that effectively results from forming an adduct between two cysteine residues, a lysine residue, and the porphyrin compound heme b, (7,12-diethenyl-3,8,13,17-tetramethylporphyrin-2,18-dipropanoato)iron." [PubMed:12709052, PubMed:9237682, RESID:AA0271]
-comment: Cross-link 3.
-synonym: "(19S,20S)-[7,12-bis((S)-1-[((R)-2-amino-2-carboxy)ethylsulfanyl]ethyl)-20-([(S)-5-amino-5-carboxypentyl]amino)-3,8,13,17-tetramethyl-21H,23H-19,20-dihydroporphine-2,18-bis(2-carboxyethyl)-N21,N22,N23,N24]-ferrate" EXACT RESID-systematic []
-synonym: "BINDING Heme (covalent; via 3 links)" EXACT UniProt-feature []
-synonym: "bis(S-cysteinyl)-N6-lysino-heme" EXACT RESID-alternate []
-synonym: "heme P460-bis-L-cysteine-L-lysine" EXACT RESID-name []
-property_value: DiffAvg "614.48" xsd:float
-property_value: DiffFormula "C 34 Fe 1 H 30 N 4 O 4 S 0" xsd:string
-property_value: DiffMono "614.161643" xsd:float
-property_value: Formula "C 46 Fe 1 H 52 N 8 O 7 S 2" xsd:string
-property_value: MassAvg "948.94" xsd:float
-property_value: MassMono "948.274976" xsd:float
-property_value: Origin "C, C, K" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00699
-is_a: MOD:02067
-is_a: MOD:02074
-
-[Term]
-id: MOD:00277
-name: 5-methyl-L-arginine
-def: "A protein modification that effectively converts an L-arginine residue to 5-methyl-L-arginine." [PubMed:10660523, PubMed:11875433, PubMed:9367957, RESID:AA0272]
-synonym: "(2S,5S)-2-amino-5-carbamimidamidohexanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-5-guanidinohexanoic acid" EXACT RESID-alternate []
-synonym: "4-methylarginine" RELATED RESID-misnomer []
-synonym: "5-methyl-L-arginine" EXACT RESID-name []
-synonym: "5-methylated L-arginine" EXACT PSI-MOD-alternate []
-synonym: "C5Me1Arg" EXACT PSI-MOD-label []
-synonym: "delta-methylarginine" EXACT RESID-alternate []
-synonym: "Methyl" RELATED PSI-MS-label []
-synonym: "Methylation" RELATED Unimod-description []
-synonym: "MOD_RES 5-methylarginine" EXACT UniProt-feature []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 7 H 14 N 4 O 1" xsd:string
-property_value: MassAvg "170.22" xsd:float
-property_value: MassMono "170.116761" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0050
-is_a: MOD:00414
-is_a: MOD:00656
-
-[Term]
-id: MOD:00278
-name: 2-methyl-L-glutamine
-def: "A protein modification that effectively converts an L-glutamine residue to 2-methyl-L-glutamine." [PubMed:10660523, PubMed:11875433, PubMed:9367957, RESID:AA0273]
-synonym: "(S)-2-amino-2-methylpentanediamic acid" EXACT RESID-systematic []
-synonym: "2-methyl-L-glutamine" EXACT RESID-name []
-synonym: "2-methylated L-glutamine" EXACT PSI-MOD-alternate []
-synonym: "2-methylglutamine" EXACT RESID-alternate []
-synonym: "alpha-methylglutamine" EXACT RESID-alternate []
-synonym: "C2MeGln" EXACT PSI-MOD-label []
-synonym: "Methyl" RELATED PSI-MS-label []
-synonym: "Methylation" RELATED Unimod-description []
-synonym: "MOD_RES 2-methylglutamine" EXACT UniProt-feature []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 6 H 10 N 2 O 2" xsd:string
-property_value: MassAvg "142.16" xsd:float
-property_value: MassMono "142.074228" xsd:float
-property_value: Origin "Q" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0016
-is_a: MOD:00656
-is_a: MOD:00722
-
-[Term]
-id: MOD:00279
-name: N-pyruvic acid 2-iminyl-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to N-pyruvic acid 2-iminyl-L-cysteine." [PubMed:1388164, RESID:AA0274, Unimod:422#C]
-subset: PSI-MOD-slim
-synonym: "(R)-2-(1-carboxy-2-sulfanylethanimino)propanoic acid" EXACT RESID-systematic []
-synonym: "MOD_RES N-pyruvate 2-iminyl-cysteine" EXACT UniProt-feature []
-synonym: "N-pyruvic acid 2-iminyl" RELATED Unimod-description []
-synonym: "N-pyruvic acid 2-iminyl-L-cysteine" EXACT RESID-name []
-synonym: "PyruvicAcidIminyl" RELATED PSI-MS-label []
-property_value: DiffAvg "70.05" xsd:float
-property_value: DiffFormula "C 3 H 2 N 0 O 2 S 0" xsd:string
-property_value: DiffMono "70.005479" xsd:float
-property_value: Formula "C 6 H 8 N 1 O 3 S 1" xsd:string
-property_value: MassAvg "174.19" xsd:float
-property_value: MassMono "174.022489" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:422
-xref: uniprot.ptm:PTM-0224
-is_a: MOD:00905
-is_a: MOD:01170
-
-[Term]
-id: MOD:00280
-name: N-pyruvic acid 2-iminyl-L-valine
-def: "A protein modification that effectively converts an L-valine residue to N-pyruvic acid 2-iminyl-L-valine." [PubMed:2071591, RESID:AA0275, Unimod:422#V]
-subset: PSI-MOD-slim
-synonym: "(S)-2-(1-carboxy-2-methylpropanimino)propanoic acid" EXACT RESID-systematic []
-synonym: "MOD_RES N-pyruvate 2-iminyl-valine" EXACT UniProt-feature []
-synonym: "N-pyruvic acid 2-iminyl" RELATED Unimod-description []
-synonym: "N-pyruvic acid 2-iminyl-L-valine" EXACT RESID-name []
-synonym: "PyruvicAcidIminyl" RELATED PSI-MS-label []
-property_value: DiffAvg "70.05" xsd:float
-property_value: DiffFormula "C 3 H 2 N 0 O 2" xsd:string
-property_value: DiffMono "70.005479" xsd:float
-property_value: Formula "C 8 H 12 N 1 O 3" xsd:string
-property_value: MassAvg "170.19" xsd:float
-property_value: MassMono "170.081718" xsd:float
-property_value: Origin "V" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:422
-xref: uniprot.ptm:PTM-0225
-is_a: MOD:00920
-is_a: MOD:01170
-
-[Term]
-id: MOD:00281
-name: 3'-heme-L-histidine
-def: "A protein modification that effectively results from forming an adduct between the pros nitrogen of a histidine residue and the porphyrin compound heme b, (7,12-diethenyl-3,8,13,17-tetramethylporphyrin-2,18-dipropanoato)iron." [PubMed:12119398, PubMed:12429096, PubMed:12486054, PubMed:9712585, RESID:AA0276]
-synonym: "2-[1-(N3'-histidyl)ethyl]protoporphyrin IX" EXACT RESID-alternate []
-synonym: "3'-heme-L-histidine" EXACT RESID-name []
-synonym: "[7-ethenyl-12-((S)-1-[((R)-2-amino-2-carboxyethyl)-3H-imidazol-3-yl]ethyl)-3,8,13,17-tetramethyl-21H,23H-porphine-2,18-bis(2-carboxyethyl)-N21,N22,N23,N24]-ferrate" EXACT RESID-systematic []
-synonym: "BINDING Heme (covalent; via pros nitrogen)" EXACT UniProt-feature []
-synonym: "N(delta)-histidyl heme" EXACT RESID-alternate []
-synonym: "N(pi)-histidyl heme" EXACT RESID-alternate []
-synonym: "N3'-histidyl heme" EXACT RESID-alternate []
-synonym: "pros-histidyl heme" EXACT RESID-alternate []
-property_value: DiffAvg "616.50" xsd:float
-property_value: DiffFormula "C 34 Fe 1 H 32 N 4 O 4" xsd:string
-property_value: DiffMono "616.177293" xsd:float
-property_value: Formula "C 40 Fe 1 H 39 N 7 O 5" xsd:string
-property_value: MassAvg "753.64" xsd:float
-property_value: MassMono "753.236205" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00699
-is_a: MOD:02070
-
-[Term]
-id: MOD:00282
-name: S-selenyl-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-selenyl-L-cysteine." [PubMed:10430865, PubMed:10966817, PubMed:11827487, PubMed:12716131, PubMed:14594807, RESID:AA0277, Unimod:423#C]
-synonym: "(R)-2-amino-3-(selanylsulfanyl)propanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-3-hydroselenosulfidopropanoic acid" EXACT RESID-alternate []
-synonym: "2-amino-3-hydroselenylsulfidopropanoic acid" EXACT RESID-alternate []
-synonym: "2-amino-3-hydroselenylthiopropanoic acid" EXACT RESID-alternate []
-synonym: "ACT_SITE S-selanylcysteine intermediate" EXACT UniProt-feature []
-synonym: "cysteine perselenide" RELATED RESID-misnomer []
-synonym: "Delta:Se(1)" RELATED PSI-MS-label []
-synonym: "MOD_RES S-selenylcysteine" EXACT UniProt-feature []
-synonym: "S-selanyl-L-cysteine" EXACT RESID-name []
-synonym: "S-selanylcysteine" EXACT RESID-alternate []
-synonym: "S-selenylcysteine" EXACT RESID-alternate []
-synonym: "selenyl" RELATED Unimod-description []
-property_value: DiffAvg "78.97" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0 S 0 Se 1" xsd:string
-property_value: DiffMono "79.916521" xsd:float
-property_value: Formula "C 3 H 5 N 1 O 1 S 1 Se 1" xsd:string
-property_value: MassAvg "182.11" xsd:float
-property_value: MassMono "182.925706" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: Unimod:423
-xref: uniprot.ptm:PTM-0282
-is_a: MOD:00745
-is_a: MOD:00778
-is_a: MOD:00905
-
-[Term]
-id: MOD:00283
-name: N6-propylamino-poly(propylmethylamino)-propyldimethylamine-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to an N6-propylamino-poly(propylmethylamino)-propyldimethylamine-L-lysine." [PubMed:10550045, PubMed:11349130, RESID:AA0278]
-synonym: "(alpha)- ([([(5S)-5-amino-5-carboxypentyl]amino)propyl][(methyl)amino])-(omega)-methyl poly[propane-1,3-diyl(methylimino)]" EXACT RESID-systematic []
-synonym: "lysine derivative Lys(x)" EXACT RESID-alternate []
-synonym: "MOD_RES N6-poly(methylaminopropyl)lysine" EXACT UniProt-feature []
-synonym: "N6-[3-([(omega)-(dimethyl)aminopropyl-poly(3-[methylamino]propyl)]amino)propyl]lysine" EXACT RESID-alternate []
-synonym: "N6-propylamino-poly(propylmethylamino)-propyldimethylamine-L-lysine" EXACT RESID-name []
-synonym: "silaffin polycationic lysine derivative" EXACT RESID-alternate []
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0198
-is_a: MOD:00912
-
-[Term]
-id: MOD:00284
-name: dihydroxyheme-L-aspartate ester-L-glutamate ester
-def: "A protein modification that effectively results from forming an adduct between an aspartic acid residue, a glutamic acid residue, and the porphyrin compound heme b, (7,12-diethenyl-3,8,13,17-tetramethylporphyrin-2,18-dipropanoato)iron." [PubMed:10447690, RESID:AA0279]
-comment: Cross-link 2.
-synonym: "1,5-bishydroxymethyl protoporphyrin IX 1-glutamate ester 5-aspartate ester" EXACT RESID-alternate []
-synonym: "[13-[(S)-(4-amino-4-carboxy)butanoyloxymethyl]-3-[(S)-(3-amino-3-carboxy)propanoyloxymethyl]-7,12-diethenyl-8,17-dimethyl-21H,23H-porphine-2,18-bis(2-carboxyethyl)-N21,N22,N23,N24]-ferrate" EXACT RESID-systematic []
-synonym: "BINDING Heme (covalent; via 2 links)" EXACT UniProt-feature []
-synonym: "dihydroxyheme-L-aspartate ester-L-glutamate ester" EXACT RESID-name []
-synonym: "peroxidase heme cofactor" EXACT RESID-alternate []
-property_value: DiffAvg "612.47" xsd:float
-property_value: DiffFormula "C 34 Fe 1 H 28 N 4 O 4" xsd:string
-property_value: DiffMono "612.145993" xsd:float
-property_value: Formula "C 43 Fe 1 H 40 N 6 O 10" xsd:string
-property_value: MassAvg "856.67" xsd:float
-property_value: MassMono "856.215529" xsd:float
-property_value: Origin "D, E" xsd:string
-property_value: Source "hypothetical" xsd:string
-is_a: MOD:00699
-is_a: MOD:02066
-is_a: MOD:02068
-
-[Term]
-id: MOD:00285
-name: dihydroxyheme-L-aspartate ester-L-glutamate ester-L-methionine sulfonium
-def: "A protein modification that effectively results from forming an adduct between an aspartic acid residue, a glutamic acid residue, a methionine residue (forming a sulfonium ether), and the porphyrin compound heme b, (7,12-diethenyl-3,8,13,17-tetramethylporphyrin-2,18-dipropanoato)iron." [PubMed:10447690, PubMed:10480885, PubMed:1320128, PubMed:7840679, RESID:AA0280]
-comment: Cross-link 3.
-synonym: "1,5-bishydroxymethyl protoporphyrin IX 1-glutamate ester 5-aspartate ester 2-methionine sulfonium" EXACT RESID-alternate []
-synonym: "[13-[(S)-(4-amino-4-carboxy)butanoyloxymethyl]-3-[(S)-(3-amino-3-carboxy)propanoyloxymethyl]-12-[(S)-(3-amino-3-carboxy)propylsulfoniumethyl]-7-ethenyl-8,17-dimethyl-21H,23H-porphine-2,18-bis(2-carboxyethyl)-N21,N22,N23,N24]-ferrate" EXACT RESID-systematic []
-synonym: "BINDING Heme (covalent; via 3 links)" EXACT UniProt-feature []
-synonym: "dihydroxyheme-L-aspartate ester-L-glutamate ester-L-methionine sulfonium" EXACT RESID-name []
-synonym: "myeloperoxidase heme cofactor" EXACT RESID-alternate []
-property_value: DiffAvg "613.47" xsd:float
-property_value: DiffFormula "C 34 Fe 1 H 29 N 4 O 4 S 0" xsd:string
-property_value: DiffMono "613.153269" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 48 Fe 1 H 50 N 7 O 11 S 1" xsd:string
-property_value: MassAvg "988.87" xsd:float
-property_value: MassMono "988.263290" xsd:float
-property_value: Origin "D, E, M" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00699
-is_a: MOD:02066
-is_a: MOD:02068
-is_a: MOD:02071
-
-[Term]
-id: MOD:00286
-name: L-cysteinyl molybdenum bis(molybdopterin guanine dinucleotide)
-def: "A protein modification that effectively converts an L-cysteine residue to L-cysteinyl molybdenum bis(molybdopterin guanine dinucleotide)." [RESID:AA0281, Unimod:424#C]
-synonym: "2-amino-5,6-dimercapto-7-methyl-3,7,8a,9-tetrahydro-8-oxa-1,3,9,10-tetraazaanthracen-4-one guanosine dinucleotide" EXACT RESID-alternate []
-synonym: "bis[8-amino-1a,2,4a,5,6,7,10-heptahydro-2-(trihydrogen diphosphate 5'-ester with guanosine)methyl-6-oxo-3,4-disulfanyl-pteridino[6,7-5,6]pyranoato-S3,S4]-cystein-S-yl-molybdenum" EXACT RESID-systematic []
-synonym: "L-cysteinyl molybdenum bis(molybdopterin guanine dinucleotide)" EXACT RESID-name []
-synonym: "molybdenum bis(molybdopterin guanine dinucleotide)" RELATED Unimod-description []
-synonym: "MolybdopterinGD" RELATED PSI-MS-label []
-property_value: DiffAvg "1572.02" xsd:float
-property_value: DiffFormula "C 40 H 47 Mo 1 N 20 O 26 P 4 S 4" xsd:string
-property_value: DiffMono "1572.985775" xsd:float
-property_value: Formula "C 43 H 52 Mo 1 N 21 O 27 P 4 S 5" xsd:string
-property_value: MassAvg "1675.15" xsd:float
-property_value: MassMono "1675.994960" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: Unimod:424
-is_a: MOD:02067
-is_a: MOD:01167
-
-[Term]
-id: MOD:00287
-name: (2S,3R,4S)-3,4-dihydroxyproline
-def: "A protein modification that effectively converts an L-proline residue to a (2S,3R,4S)-3,4-dihydroxyproline." [DeltaMass:0, PubMed:12686488, RESID:AA0282, Unimod:425#P, ChEBI:141803]
-comment: From DeltaMass: Average Mass: 32.
-synonym: "(2S,3R,4S)-3,4-dihydroxyproline" EXACT RESID-name []
-synonym: "(2S,3R,4S)-3,4-dihydroxypyrrolidine-2-carboxylic acid" EXACT RESID-systematic []
-synonym: "2,3-trans-3,4-cis-3,4-dihydroxy-L-proline" EXACT RESID-alternate []
-synonym: "2-alpha-3-beta-4-beta-3,4-dihydroxyproline" EXACT RESID-alternate []
-synonym: "3,4-dihydroxylated L-proline" EXACT PSI-MOD-alternate []
-synonym: "3,4-Dihydroxylation (of Proline)" EXACT DeltaMass-label []
-synonym: "34Hy2Pro" EXACT PSI-MOD-label []
-synonym: "dihydroxy" RELATED Unimod-description []
-synonym: "Dioxidation" RELATED PSI-MS-label []
-synonym: "MOD_RES (3R,4S)-3,4-dihydroxyproline" EXACT UniProt-feature []
-synonym: "trans-2,3-cis-3,4-dihydroxy-L-proline" EXACT RESID-alternate []
-property_value: DiffAvg "32.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 2" xsd:string
-property_value: DiffMono "31.989829" xsd:float
-property_value: Formula "C 5 H 7 N 1 O 3" xsd:string
-property_value: MassAvg "129.12" xsd:float
-property_value: MassMono "129.042593" xsd:float
-property_value: Origin "P" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:425
-xref: uniprot.ptm:PTM-0306
-is_a: MOD:00866
-
-[Term]
-id: MOD:00288
-name: pyrroloquinoline quinone
-def: "A protein modification that effectively doubly cross-links an L-glutamic acid residue and an L-tyrosine residue with a carbon-carbon bond and a carbon-nitrogen bond to form pyrroloquinoline quinone." [ChEBI:18315, PubMed:1310505, PubMed:7665488, RESID:AA0283]
-comment: Cross-link 2.
-synonym: "2,4,6-tricarboxylic-pyrrolo[2,3-5,6]quinoline 8,9-quinone" EXACT RESID-alternate []
-synonym: "2,7,9-tricarboxy-1H-pyrrolo(2,3-f)quinoline-4,5-dione" EXACT RESID-alternate []
-synonym: "4,5-dihydro-4,5-dioxo-1H-pyrrolo[2,3-5,6]quinoline-2,7,9-tricarboxylic acid" EXACT RESID-systematic []
-synonym: "coenzyme PQQ" EXACT RESID-alternate []
-synonym: "CROSSLNK Pyrroloquinoline quinone (Glu-Tyr)" EXACT UniProt-feature []
-synonym: "methoxatin" EXACT RESID-alternate []
-synonym: "pyrroloquinoline quinone" EXACT RESID-name []
-property_value: DiffAvg "37.92" xsd:float
-property_value: DiffFormula "C 0 H -10 N 0 O 3" xsd:string
-property_value: DiffMono "37.906494" xsd:float
-property_value: Formula "C 14 H 6 N 2 O 8" xsd:string
-property_value: MassAvg "330.21" xsd:float
-property_value: MassMono "330.012415" xsd:float
-property_value: Origin "E, Y" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0263
-is_a: MOD:00692
-is_a: MOD:02045
-is_a: MOD:02058
-
-[Term]
-id: MOD:00289
-name: tris-L-cysteinyl L-N1'-histidino tetrairon tetrasulfide
-def: "A protein modification that effectively converts three L-cysteine residues, an L-histidine residue and a four-iron four-sulfur cluster to tris-L-cysteinyl L-N1'-histidino tetrairon tetrasulfide." [PubMed:9836629, RESID:AA0284]
-comment: Cross-link 4.
-synonym: "METAL Iron-sulfur (4Fe-4S)" EXACT UniProt-feature []
-synonym: "METAL Iron-sulfur (4Fe-4S); via tele nitrogen" EXACT UniProt-feature []
-synonym: "tetra-mu3-sulfidotris(S-cysteinyliron)(N1'-histidinoiron)" EXACT RESID-systematic []
-synonym: "tris-L-cysteinyl L-N1'-histidino tetrairon tetrasulfide" EXACT RESID-name []
-property_value: DiffAvg "347.59" xsd:float
-property_value: DiffFormula "C 0 Fe 4 H -4 N 0 O 0 S 4" xsd:string
-property_value: DiffMono "347.597831" xsd:float
-property_value: FormalCharge "2-" xsd:string
-property_value: Formula "C 15 Fe 4 H 18 N 6 O 4 S 7" xsd:string
-property_value: MassAvg "794.15" xsd:float
-property_value: MassMono "793.684297" xsd:float
-property_value: Origin "C, C, C, H" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00739
-is_a: MOD:02067
-is_a: MOD:02070
-
-[Term]
-id: MOD:00290
-name: tris-L-cysteinyl L-N3'-histidino tetrairon tetrasulfide
-def: "A protein modification that effectively converts three L-cysteine residues, an L-histidine residue and a four-iron four-sulfur cluster to tris-L-cysteinyl L-N3'-histidino tetrairon tetrasulfide." [PubMed:7854413, RESID:AA0285]
-comment: Cross-link 4.
-synonym: "METAL Iron-sulfur (4Fe-4S)" EXACT UniProt-feature []
-synonym: "METAL Iron-sulfur (4Fe-4S); via pros nitrogen" EXACT UniProt-feature []
-synonym: "tetra-mu3-sulfidotris(S-cysteinyliron)(N3'-histidinoiron)" EXACT RESID-systematic []
-synonym: "tris-L-cysteinyl L-N3'-histidino tetrairon tetrasulfide" EXACT RESID-name []
-property_value: DiffAvg "347.59" xsd:float
-property_value: DiffFormula "C 0 Fe 4 H -4 N 0 O 0 S 4" xsd:string
-property_value: DiffMono "347.597831" xsd:float
-property_value: FormalCharge "2-" xsd:string
-property_value: Formula "C 15 Fe 4 H 18 N 6 O 4 S 7" xsd:string
-property_value: MassAvg "794.15" xsd:float
-property_value: MassMono "793.684297" xsd:float
-property_value: Origin "C, C, C, H" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00739
-is_a: MOD:02067
-is_a: MOD:02070
-
-[Term]
-id: MOD:00291
-name: tris-L-cysteinyl L-aspartato tetrairon tetrasulfide
-def: "A protein modification that effectively converts three L-cysteine residues, an L-aspartic acid residue and a four-iron four-sulfur cluster to tris-L-cysteinyl L-aspartato tetrairon tetrasulfide." [PubMed:7819255, PubMed:9283079, RESID:AA0286]
-comment: Cross-link 4.
-synonym: "METAL Iron-sulfur (4Fe-4S)" EXACT UniProt-feature []
-synonym: "tetra-mu3-sulfidotris(S-cysteinyliron)(O4-aspartatoiron)" EXACT RESID-systematic []
-synonym: "tris-L-cysteinyl L-aspartato tetrairon tetrasulfide" EXACT RESID-name []
-property_value: DiffAvg "347.59" xsd:float
-property_value: DiffFormula "C 0 Fe 4 H -4 N 0 O 0 S 4" xsd:string
-property_value: DiffMono "347.597831" xsd:float
-property_value: FormalCharge "2-" xsd:string
-property_value: Formula "C 13 Fe 4 H 16 N 4 O 6 S 7" xsd:string
-property_value: MassAvg "772.09" xsd:float
-property_value: MassMono "771.652328" xsd:float
-property_value: Origin "C, C, C, D" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00739
-is_a: MOD:02066
-is_a: MOD:02067
-
-[Term]
-id: MOD:00292
-name: N6-pyruvic acid 2-iminyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-pyruvic acid 2-iminyl-L-lysine." [PubMed:1463470, PubMed:7853400, PubMed:9047371, RESID:AA0287, Unimod:422#K]
-synonym: "(2S)-2-amino-6-([1-carboxyethylidene]amino)hexanoic acid" EXACT RESID-systematic []
-synonym: "ACT_SITE Schiff-base intermediate with substrate" EXACT UniProt-feature []
-synonym: "N-pyruvic acid 2-iminyl" RELATED Unimod-description []
-synonym: "N6-pyruvic acid 2-iminyl-L-lysine" EXACT RESID-name []
-synonym: "PyruvicAcidIminyl" RELATED PSI-MS-label []
-property_value: DiffAvg "70.05" xsd:float
-property_value: DiffFormula "C 3 H 2 N 0 O 2" xsd:string
-property_value: DiffMono "70.005479" xsd:float
-property_value: Formula "C 9 H 14 N 2 O 3" xsd:string
-property_value: MassAvg "198.22" xsd:float
-property_value: MassMono "198.100442" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:422
-is_a: MOD:00912
-is_a: MOD:01170
-
-[Term]
-id: MOD:00293
-name: tris-L-cysteinyl L-serinyl tetrairon tetrasulfide
-def: "A protein modification that effectively converts three L-cysteine residues, an L-serine residue and a four-iron four-sulfur cluster to tris-L-cysteinyl L-serinyl tetrairon tetrasulfide." [RESID:AA0288]
-comment: Cross-link 4.
-synonym: "tetra-mu3-sulfidotris(S-cysteinyliron)(O3-serinyliron)" EXACT RESID-systematic []
-synonym: "tris-L-cysteinyl L-serinyl tetrairon tetrasulfide" EXACT RESID-name []
-property_value: DiffAvg "347.59" xsd:float
-property_value: DiffFormula "C 0 Fe 4 H -4 N 0 O 0 S 4" xsd:string
-property_value: DiffMono "347.597831" xsd:float
-property_value: FormalCharge "2-" xsd:string
-property_value: Formula "C 12 Fe 4 H 16 N 4 O 5 S 7" xsd:string
-property_value: MassAvg "744.08" xsd:float
-property_value: MassMono "743.657414" xsd:float
-property_value: Origin "C, C, C, S" xsd:string
-property_value: Source "hypothetical" xsd:string
-is_a: MOD:00739
-is_a: MOD:02067
-is_a: MOD:02072
-
-[Term]
-id: MOD:00294
-name: bis-L-cysteinyl L-N3'-histidino L-serinyl tetrairon tetrasulfide
-def: "A protein modification that effectively converts two L-cysteine residues, an L-histidine residues, an L-serine residue and a four-iron four-sulfur cluster to bis-L-cysteinyl L-N3'-histidino L-serinyl tetrairon tetrasulfide." [RESID:AA0289]
-comment: Cross-link 4.
-synonym: "bis-L-cysteinyl L-N3'-histidino L-serinyl tetrairon tetrasulfide" EXACT RESID-name []
-synonym: "METAL Iron-sulfur (4Fe-4S)" EXACT UniProt-feature []
-synonym: "METAL Iron-sulfur (4Fe-4S); via pros nitrogen" EXACT UniProt-feature []
-synonym: "tetra-mu3-sulfidobis(S-cysteinyliron)(N3'-histidinoiron)(O3-serinyliron)" EXACT RESID-systematic []
-property_value: DiffAvg "347.59" xsd:float
-property_value: DiffFormula "C 0 Fe 4 H -4 N 0 O 0 S 4" xsd:string
-property_value: DiffMono "347.597831" xsd:float
-property_value: FormalCharge "2-" xsd:string
-property_value: Formula "C 15 Fe 4 H 18 N 6 O 5 S 6" xsd:string
-property_value: MassAvg "778.09" xsd:float
-property_value: MassMono "777.707141" xsd:float
-property_value: Origin "C, C, H, S" xsd:string
-property_value: Source "hypothetical" xsd:string
-is_a: MOD:00739
-is_a: MOD:02067
-is_a: MOD:02070
-is_a: MOD:02072
-
-[Term]
-id: MOD:00295
-name: O-octanoyl-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O-octanoyl-L-serine." [PubMed:10604470, PubMed:12716131, RESID:AA0290, Unimod:426#S]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-(octanoyloxy)propanoic acid" EXACT RESID-systematic []
-synonym: "L-serine octanoate ester" EXACT RESID-alternate []
-synonym: "LIPID O-octanoyl serine" EXACT UniProt-feature []
-synonym: "O-octanoyl-L-serine" EXACT RESID-name []
-synonym: "O-octanoylated L-serine" EXACT PSI-MOD-alternate []
-synonym: "O3-octanoyl-L-serine" EXACT RESID-alternate []
-synonym: "Octanoyl" RELATED PSI-MS-label []
-synonym: "octanoyl" RELATED Unimod-description []
-synonym: "OOctSer" EXACT PSI-MOD-label []
-property_value: DiffAvg "126.20" xsd:float
-property_value: DiffFormula "C 8 H 14 N 0 O 1" xsd:string
-property_value: DiffMono "126.104465" xsd:float
-property_value: Formula "C 11 H 19 N 1 O 3" xsd:string
-property_value: MassAvg "213.28" xsd:float
-property_value: MassMono "213.136493" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:426
-xref: uniprot.ptm:PTM-0239
-is_a: MOD:00669
-is_a: MOD:02003
-
-[Term]
-id: MOD:00296
-name: O-D-glucuronosyl-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O-D-glucuronosyl-L-serine." [PubMed:10858503, PubMed:12716131, PubMed:7398618, RESID:AA0291, Unimod:54#S]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-(beta-D-glucopyranuronosyl)propanoic acid" EXACT RESID-systematic []
-synonym: "CARBOHYD O-linked (GlcA) serine" EXACT UniProt-feature []
-synonym: "Glucuronyl" RELATED PSI-MS-label []
-synonym: "N-glucuronylation" RELATED Unimod-description []
-synonym: "O-D-glucuronosyl-L-serine" EXACT RESID-name []
-synonym: "O3-D-glucuronosyl-L-serine" EXACT RESID-alternate []
-property_value: DiffAvg "176.12" xsd:float
-property_value: DiffFormula "C 6 H 8 N 0 O 6" xsd:string
-property_value: DiffMono "176.032088" xsd:float
-property_value: Formula "C 9 H 13 N 1 O 8" xsd:string
-property_value: MassAvg "263.20" xsd:float
-property_value: MassMono "263.064116" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:54
-xref: uniprot.ptm:PTM-0577
-is_a: MOD:00447
-is_a: MOD:00916
-
-[Term]
-id: MOD:00297
-name: tris-L-cysteinyl L-cysteine persulfido bis-L-glutamato L-histidino nickel triiron disulfide trioxide
-def: "A protein modification that effectively converts four L-cysteine residues, two L-glutamic acid residues, an L-histidine residue and a three-iron three-sulfur three-oxygen cluster to tris-L-cysteinyl L-cysteine persulfido bis-L-glutamato L-histidino nickel triiron disulfide trioxide." [RESID:AA0292]
-comment: Cross-link 7; secondary to RESID:AA0269. This is a deprecated entry in RESID. It probably does not occur naturally [JSG].
-synonym: "carbon monoxide dehydrogenase nickel-iron cofactor" EXACT RESID-alternate []
-synonym: "hybrid nickel-triiron cluster" EXACT RESID-alternate []
-synonym: "mu-1:2kappaO-oxido-mu-1:3kappaO-oxido-mu-2:4kappaO-oxido-mu-3:4kappaS-sulfido-mu3-2:3:4kappaS-sulfido-S-cysteinyl-N1'-histidino-O5-glutamato 1-iron-S5-cysteine persulfido-O5-glutamato 2-nickel-3,4-bis-(S-cysteinyl iron)" EXACT RESID-systematic []
-synonym: "Ni-3Fe-2S-3O cluster" EXACT RESID-alternate []
-synonym: "tris-L-cysteinyl L-cysteine persulfido bis-L-glutamato L-histidino nickel triiron disulfide trioxide" EXACT RESID-name []
-property_value: DiffAvg "363.35" xsd:float
-property_value: DiffFormula "C 0 Fe 3 H -7 N 0 Ni 1 O 3 S 3" xsd:string
-property_value: DiffMono "362.586337" xsd:float
-property_value: Formula "C 28 Fe 3 H 34 N 9 Ni 1 O 14 S 7" xsd:string
-property_value: MassAvg "1171.28" xsd:float
-property_value: MassMono "1169.767174" xsd:float
-property_value: Origin "C, C, C, C, E, E, H" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00739
-is_a: MOD:00741
-is_a: MOD:02067
-is_a: MOD:02068
-is_a: MOD:02070
-
-[Term]
-id: MOD:00298
-name: tris-L-cysteinyl L-cysteine persulfido L-glutamato L-histidino L-serinyl nickel triiron disulfide trioxide
-def: "A protein modification that effectively converts four L-cysteine residues, an L-glutamic acid residue, an L-histidine residue, an L-serine residue and a one-nickel three-iron three-sulfur three-oxygen cluster to tris-L-cysteinyl L-cysteine persulfido L-glutamato L-histidino L-serinyl nickel triiron disulfide trioxide." [PubMed:2550436, RESID:AA0293]
-comment: Cross-link 7; secondary to RESID:AA0269. This is a deprecated entry in RESID. It probably does not occur naturally [JSG].
-synonym: "carbon monoxide dehydrogenase nickel-iron cofactor" EXACT RESID-alternate []
-synonym: "hybrid nickel-triiron cluster" EXACT RESID-alternate []
-synonym: "mu-1:2kappaO-oxido-mu-1:3kappaO-oxido-mu-2:4kappaO-oxido-mu-3:4kappaS-sulfido-mu3-2:3:4kappaS-sulfido-S-cysteinyl-N1'-histidino-O5-glutamato 1-iron-S5-cysteine persulfido-O3-serinyl 2-nickel-3,4-bis-(S-cysteinyl iron)" EXACT RESID-systematic []
-synonym: "Ni-3Fe-2S-3O cluster" EXACT RESID-alternate []
-synonym: "tris-L-cysteinyl L-cysteine persulfido L-glutamato L-histidino L-serinyl nickel triiron disulfide trioxide" EXACT RESID-name []
-property_value: DiffAvg "363.35" xsd:float
-property_value: DiffFormula "C 0 Fe 3 H -7 N 0 Ni 1 O 3 S 3" xsd:string
-property_value: DiffMono "362.586337" xsd:float
-property_value: Formula "C 26 Fe 3 H 32 N 9 Ni 1 O 13 S 7" xsd:string
-property_value: MassAvg "1129.24" xsd:float
-property_value: MassMono "1127.756609" xsd:float
-property_value: Origin "C, C, C, C, E, H, S" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00739
-is_a: MOD:00741
-is_a: MOD:02067
-is_a: MOD:02068
-is_a: MOD:02070
-is_a: MOD:02072
-
-[Term]
-id: MOD:00299
-name: N6-(L-isoaspartyl)-L-lysine (Asn)
-def: "A protein modification that effectively crosslinks an L-asparagine residue and an L-lysine residue by an isopeptide bond with the formation of N6-(L-isoaspartyl)-L-lysine and the release of ammonia." [ChEBI:21862, DeltaMass:0, PubMed:11000116, PubMed:6503713, RESID:AA0294]
-comment: Cross-link 2.
-synonym: "(2S)-2-amino-6-([(3S)-3-amino-3-carboxypropanoyl]amino)hexanoic acid" EXACT RESID-systematic []
-synonym: "beta-(N6-lysyl)aspartyl acid" EXACT RESID-alternate []
-synonym: "CROSSLNK Isoaspartyl lysine isopeptide (Lys-Asn)" EXACT UniProt-feature []
-synonym: "isoaspartyl N6-lysine" EXACT RESID-alternate []
-synonym: "N(epsilon)-(beta-aspartyl)lysine" EXACT RESID-alternate []
-synonym: "N-(beta-Aspartyl)-Lysine (Crosslink)" EXACT DeltaMass-label []
-synonym: "N6-(L-isoaspartyl)-L-lysine" EXACT RESID-name []
-synonym: "XLNK-4Asp-N6Lys(Asn)" EXACT PSI-MOD-label []
-property_value: DiffAvg "-17.03" xsd:float
-property_value: DiffFormula "C 0 H -3 N -1 O 0" xsd:string
-property_value: DiffMono "-17.026549" xsd:float
-property_value: Formula "C 10 H 15 N 3 O 3" xsd:string
-property_value: MassAvg "225.25" xsd:float
-property_value: MassMono "225.111341" xsd:float
-property_value: Origin "K, N" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0153
-is_a: MOD:02042
-is_a: MOD:00946
-is_a: MOD:01929
-
-[Term]
-id: MOD:00300
-name: L-glutamyl-5-poly(ADP-ribose)
-def: "A protein modification that effectively converts an L-glutamic acid residue to L-glutamyl-5-poly(ADP-ribose)." [DeltaMass:0, PubMed:11246023, PubMed:15842200, PubMed:8533153, RESID:AA0295, Unimod:213#E]
-synonym: "(S)-2-amino-5-poly[2'-adenosine 5'-(trihydrogen diphosphate) 5'->5'-ester with 1alpha-D-ribofuranosyl]oxy-5-oxopentanoic acid" EXACT RESID-systematic []
-synonym: "ADP Ribose addition" RELATED Unimod-description []
-synonym: "ADP-Ribosyl" RELATED PSI-MS-label []
-synonym: "L-glutamyl-5-poly(ADP-ribose)" EXACT RESID-name []
-synonym: "L-isoglutamyl-poly(ADP-ribose)" EXACT RESID-alternate []
-synonym: "MOD_RES PolyADP-ribosyl glutamic acid" EXACT UniProt-feature []
-synonym: "O-ADP-ribosylation (on Glutamate or C terminus)" EXACT DeltaMass-label []
-property_value: Origin "E" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:213
-is_a: MOD:02087
-is_a: MOD:00906
-
-[Term]
-id: MOD:00301
-name: O-(N-acetylglucosamine-1-phosphoryl)-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O-(N-acetylglucosamine-1-phosphoryl)-L-serine." [DeltaMass:0, PubMed:6438439, PubMed:6993483, PubMed:8631906, RESID:AA0296, Unimod:428]
-synonym: "(2S)-2-amino-3-[([(2-acetamido-2-deoxy-alpha-D-glucopyranosyl)oxy][hydroxy]phosphoryl)oxy]propanoic acid" EXACT RESID-systematic []
-synonym: "N-acetylglucosamine-1-phosphoryl" RELATED Unimod-description []
-synonym: "O-(N-acetylglucosamine-1-phosphoryl)-L-serine" EXACT RESID-name []
-synonym: "O-beta(N-acetyl-glucosamine-alpha1-phosphate)serine" EXACT RESID-alternate []
-synonym: "O-GlcNAc-1-phosphorylation (of Serine)" EXACT DeltaMass-label []
-synonym: "O3-(N-acetylglucosamine-1-phosphoryl)-L-serine" EXACT RESID-alternate []
-synonym: "O3-L-serine 2-(acetylamino)-2-deoxy-D-glucopyranose 1-phosphodiester" EXACT RESID-alternate []
-synonym: "PhosphoHexNAc" RELATED PSI-MS-label []
-synonym: "CARBOHYD O-linked (GalNAcP) serine" EXACT UniProt-feature []
-property_value: DiffAvg "283.17" xsd:float
-property_value: DiffFormula "C 8 H 14 N 1 O 8 P 1" xsd:string
-property_value: DiffMono "283.045703" xsd:float
-property_value: Formula "C 11 H 19 N 2 O 10 P 1" xsd:string
-property_value: MassAvg "370.25" xsd:float
-property_value: MassMono "370.077731" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:428
-xref: uniprot.ptm:PTM-0586
-is_a: MOD:00916
-is_a: MOD:01804
-
-[Term]
-id: MOD:00302
-name: O-(phosphoglycosyl-D-mannose-1-phosphoryl)-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O-(phosphoglycosyl-D-mannose-1-phosphoryl)-L-serine." [PubMed:10037765, PubMed:15649890, RESID:AA0297, Unimod:429]
-synonym: "O-(alpha-D-mannosyl-1-phosphoryl)-L-serine" EXACT RESID-alternate []
-synonym: "O-(D-mannose-1-phosphoryl)-L-serine" EXACT RESID-name []
-synonym: "O-[alpha-D-mannopyranosyloxy(hydroxy)phosphoryl]-L-serine" EXACT RESID-systematic []
-synonym: "O3-(D-mannose-1-phosphoryl)-L-serine" EXACT RESID-alternate []
-synonym: "O3-L-serine alpha-D-mannopyranose 1-phosphodiester" EXACT RESID-alternate []
-synonym: "phosphoglycosyl-D-mannose-1-phosphoryl" RELATED Unimod-description []
-synonym: "PhosphoHex" RELATED PSI-MS-label []
-synonym: "CARBOHYD O-linked (Man1P) serine" EXACT UniProt-feature []
-property_value: DiffAvg "242.12" xsd:float
-property_value: DiffFormula "C 6 H 11 N 0 O 8 P 1" xsd:string
-property_value: DiffMono "242.019154" xsd:float
-property_value: Formula "C 9 H 16 N 1 O 10 P 1" xsd:string
-property_value: MassAvg "329.20" xsd:float
-property_value: MassMono "329.051182" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:429
-xref: uniprot.ptm:PTM-0594
-is_a: MOD:00916
-is_a: MOD:01804
-
-[Term]
-id: MOD:00303
-name: heptakis-L-histidino tetracopper mu4-sulfide hydroxide
-def: "A protein modification that effectively converts seven L-histidinine residues and a four-copper one-sulfur one-hydroxide cluster to heptakis-L-histidino tetracopper mu4-sulfide hydroxide." [PubMed:11024061, PubMed:11041839, RESID:AA0298]
-comment: Cross-link 7.
-synonym: "heptakis-L-histidino tetracopper mu4-sulfide hydroxide" EXACT RESID-name []
-synonym: "mu4-sulfido bis(bis-N1'-histidino copper)(N1'-histidino-N3'-histidino copper)(N3'-histidino hydroxide copper)" EXACT RESID-systematic []
-synonym: "nitrous oxide reductase nosZ CuZ cluster" EXACT RESID-alternate []
-synonym: "pentakis-L-N1'-histidino-bis-L-N3'-histidino tetracopper sulfide hydroxide" EXACT RESID-alternate []
-property_value: DiffAvg "296.19" xsd:float
-property_value: DiffFormula "C 0 Cu 4 H -6 N 0 O 1 S 1" xsd:string
-property_value: DiffMono "293.638425" xsd:float
-property_value: Formula "C 42 Cu 4 H 43 N 21 O 8 S 1" xsd:string
-property_value: MassAvg "1256.19" xsd:float
-property_value: MassMono "1253.050808" xsd:float
-property_value: Origin "H, H, H, H, H, H, H" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00742
-is_a: MOD:00860
-is_a: MOD:02070
-
-[Term]
-id: MOD:00304
-name: L-leucine methyl ester
-def: "A protein modification that effectively converts an L-leucine residue to L-leucine methyl ester." [PubMed:10191253, PubMed:11875433, PubMed:8206937, RESID:AA0299, Unimod:34#C-term]
-comment: incidental to RESID:AA0039
-subset: PSI-MOD-slim
-synonym: "2-amino-4-methylpentanoic methyl ester" EXACT RESID-alternate []
-synonym: "alpha-aminoisocaproic methyl ester" EXACT RESID-alternate []
-synonym: "L-leucine methyl ester" EXACT RESID-name []
-synonym: "Methyl" RELATED PSI-MS-label []
-synonym: "methyl (2S)-2-amino-4-methylpentanoate" EXACT RESID-systematic []
-synonym: "methyl esterified L-leucine" EXACT PSI-MOD-alternate []
-synonym: "methyl L-leucinate" EXACT RESID-alternate []
-synonym: "Methylation" RELATED Unimod-description []
-synonym: "MOD_RES Leucine methyl ester" EXACT UniProt-feature []
-synonym: "OMeLeu" EXACT PSI-MOD-label []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 7 H 14 N 1 O 2" xsd:string
-property_value: MassAvg "144.19" xsd:float
-property_value: MassMono "144.102454" xsd:float
-property_value: Origin "L" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: Unimod:34
-xref: uniprot.ptm:PTM-0167
-is_a: MOD:00599
-is_a: MOD:00662
-is_a: MOD:01689
-
-[Term]
-id: MOD:00305
-name: hexakis-L-cysteinyl L-serinyl octairon heptasulfide
-def: "A protein modification that effectively converts six L-cysteine residues, an L-serine residue and a eight-iron seven-sulfur cluster to hexakis-L-cysteinyl L-serinyl octairon heptasulfide." [PubMed:10525412, PubMed:12215645, PubMed:9063865, RESID:AA0300]
-comment: Cross-link 7; incidental to RESID:AA0141.
-synonym: "Cys6Ser-[8Fe7S]" EXACT PSI-MOD-label []
-synonym: "hexakis-L-cysteinyl L-serinyl octairon heptasulfide" EXACT RESID-name []
-synonym: "METAL Iron-sulfur (8Fe-7S)" EXACT UniProt-feature []
-synonym: "nitrogenase P-cluster" EXACT RESID-alternate []
-property_value: DiffAvg "663.12" xsd:float
-property_value: DiffFormula "C 0 Fe 8 H -8 N 0 O 0 S 7" xsd:string
-property_value: DiffMono "663.223042" xsd:float
-property_value: FormalCharge "3-" xsd:string
-property_value: Formula "C 21 Fe 8 H 27 N 7 O 8 S 13" xsd:string
-property_value: MassAvg "1369.03" xsd:float
-property_value: MassMono "1368.310179" xsd:float
-property_value: Origin "C, C, C, C, C, C, S" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00739
-is_a: MOD:02067
-is_a: MOD:02072
-
-[Term]
-id: MOD:00306
-name: residues isobaric at 113.084064 Da
-def: "Natural or modified residues with a mass of 113.084064 Da." [PubMed:10523135, RESID:AA0301]
-subset: PSI-MOD-slim
-synonym: "L-isoleucine or L-leucine" EXACT RESID-name []
-synonym: "Xle" EXACT PSI-MOD-label []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 6 H 11 N 1 O 1" xsd:string
-property_value: MassAvg "113.16" xsd:float
-property_value: MassMono "113.084064" xsd:float
-property_value: Origin "X" xsd:string
-is_a: MOD:00569
-is_a: MOD:00624
-
-[Term]
-id: MOD:00307
-name: L-aspartimide
-def: "A protein modification that effectively cyclizes an L-asparagine residue to form a carboxyl-terminal L-aspartimide." [DeltaMass:18, PubMed:12771378, PubMed:2378679, PubMed:7662664, PubMed:7988548, PubMed:9309583, RESID:AA0302, Unimod:23#N]
-comment: From DeltaMass: Average Mass: -17 Average Mass Change:-17 References:Clarke, S., Lability of Aspargine and Aspartic Acid Residues in Protein and Peptides, in: Stability of Protein Pharmaceuticals : Chemical and Physical Paths of Protein Degradation, Part A (T.J. Ahern and M.C. Manning, eds.), 1992,Plenum Press, New York, pp.1-29Xie, M.; Vander Velde, D.; Morton, M.; Borchardt, R.T.; Schowen,R.L.: pH-Induced Change in the Rate-Determining Step for the Hydrolysis of the Asp/Asn-Derived Cyclic-Imide Intermediate in Protein Degradation. (1996) J. Am. Chem. Soc. 118: 8955-8956.
-synonym: "(3S)-3-amino-2,5-pyrrolidinedione" EXACT RESID-systematic []
-synonym: "2-amino-butanimide" EXACT RESID-alternate []
-synonym: "alpha-aminosuccinimide" EXACT RESID-alternate []
-synonym: "ASI" EXACT RESID-alternate []
-synonym: "Dehydrated" RELATED Unimod-interim []
-synonym: "Dehydration" RELATED Unimod-description []
-synonym: "L-2-aminosuccinimide" EXACT RESID-alternate []
-synonym: "L-3-aminosuccinimide" RELATED RESID-misnomer []
-synonym: "L-asparaginimide" EXACT RESID-alternate []
-synonym: "L-aspartimide" EXACT RESID-name []
-synonym: "Succinimide formation from asparagine" EXACT DeltaMass-label []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 4 H 5 N 2 O 2" xsd:string
-property_value: MassAvg "113.10" xsd:float
-property_value: MassMono "113.035102" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: Unimod:23
-is_a: MOD:00601
-is_a: MOD:00704
-is_a: MOD:00903
-
-[Term]
-id: MOD:00308
-name: L-glutamimide
-def: "A protein modification that effectively cyclizes an L-glutamine residue to form a carboxyl-terminal L-glutamimide." [PubMed:12771378, PubMed:14593103, RESID:AA0303, Unimod:23#Q]
-synonym: "(3S)-3-aminopiperidine-2,6-dione" EXACT RESID-systematic []
-synonym: "2-aminopentanimide" EXACT RESID-alternate []
-synonym: "3-amino-2,6-piperidinedione" EXACT RESID-alternate []
-synonym: "alpha-aminoglutarimide" EXACT RESID-alternate []
-synonym: "Dehydrated" RELATED Unimod-interim []
-synonym: "Dehydration" RELATED Unimod-description []
-synonym: "L-glutamimide" EXACT RESID-name []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 5 H 7 N 2 O 2" xsd:string
-property_value: MassAvg "127.12" xsd:float
-property_value: MassMono "127.050752" xsd:float
-property_value: Origin "Q" xsd:string
-property_value: Source "hypothetical" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: Unimod:23
-is_a: MOD:00601
-is_a: MOD:00704
-is_a: MOD:00907
-
-[Term]
-id: MOD:00309
-name: L-beta-carboxyaspartic acid
-def: "A protein modification that effectively converts an L-aspartic acid residue to L-beta-carboxyaspartic acid." [OMSSA:47, PubMed:6390094, PubMed:7138832, PubMed:7457858, PubMed:8135347, RESID:AA0304, Unimod:299#D]
-comment: References to this modification as a gamma-carboxylation are in error [JSG].
-synonym: "(2S)-2-aminoethane-1,1,2-tricarboxylic acid" EXACT RESID-systematic []
-synonym: "2-amino-3-carboxybutanedioic acid" EXACT RESID-alternate []
-synonym: "3-carboxy-L-aspartic acid" EXACT RESID-name []
-synonym: "3-carboxyaspartic acid" EXACT RESID-alternate []
-synonym: "3CbxAsp" EXACT PSI-MOD-label []
-synonym: "beta-carboxyaspartic acid" EXACT RESID-alternate []
-synonym: "Carboxy" RELATED PSI-MS-label []
-synonym: "Carboxy" RELATED Unimod-interim []
-synonym: "Carboxylation" RELATED Unimod-description []
-synonym: "gammacarboxyld" EXACT OMSSA-label []
-property_value: DiffAvg "44.01" xsd:float
-property_value: DiffFormula "C 1 H 0 N 0 O 2" xsd:string
-property_value: DiffMono "43.989829" xsd:float
-property_value: Formula "C 5 H 5 N 1 O 5" xsd:string
-property_value: MassAvg "159.10" xsd:float
-property_value: MassMono "159.016772" xsd:float
-property_value: Origin "D" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: Unimod:299
-is_a: MOD:00904
-is_a: MOD:01152
-
-[Term]
-id: MOD:00310
-name: N5-methyl-L-arginine
-def: "A protein modification that effectively converts an L-arginine residue to N5-methyl-L-arginine." [PubMed:11875433, PubMed:9792625, PubMed:9873020, RESID:AA0305]
-synonym: "(2S)-2-amino-5-(N-methylcarbamimidamido)pentanoic acid" EXACT RESID-systematic []
-synonym: "delta-N-methylarginine" EXACT RESID-alternate []
-synonym: "Methyl" RELATED PSI-MS-label []
-synonym: "Methylation" RELATED Unimod-description []
-synonym: "MOD_RES N5-methylarginine" EXACT UniProt-feature []
-synonym: "N5-carbamimidoyl-N5-methyl-L-ornithine" EXACT RESID-alternate []
-synonym: "N5-methyl-L-arginine" EXACT RESID-name []
-synonym: "N5-methylated L-arginine" EXACT PSI-MOD-alternate []
-synonym: "N5Me1Arg" EXACT PSI-MOD-label []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 7 H 14 N 4 O 1" xsd:string
-property_value: MassAvg "170.22" xsd:float
-property_value: MassMono "170.116761" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: uniprot.ptm:PTM-0185
-is_a: MOD:00414
-is_a: MOD:00602
-
-[Term]
-id: MOD:00311
-name: L-cysteine coenzyme A disulfide
-def: "A protein modification that effectively converts an L-cysteine residue to L-cysteine coenzyme A disulfide." [DeltaMass:0, PubMed:1734967, RESID:AA0306, Unimod:281#C]
-comment: DeltaMass gives no formula with mass as 454.
-synonym: "(2R)-2-amino-3-(2-((3-(((2R)-2,4-dihydroxy-3,3-dimethyl-1-oxobutyl)amino)-1-oxopropyl)amino)ethyl)dithio-propanoic acid 4'-ester with adenosine 5'-(trihydrogen diphosphate) 3'-(dihydrogen phosphate)" EXACT RESID-systematic []
-synonym: "coenzyme A L-cysteine mixed disulfide" EXACT RESID-alternate []
-synonym: "CoenzymeA" RELATED PSI-MS-label []
-synonym: "Cysteine modified Coenzyme A" RELATED Unimod-description []
-synonym: "L-cysteine coenzyme A disulfide" EXACT RESID-name []
-synonym: "SCoACys" EXACT PSI-MOD-label []
-property_value: DiffAvg "765.52" xsd:float
-property_value: DiffFormula "C 21 H 34 N 7 O 16 P 3 S 1" xsd:string
-property_value: DiffMono "765.099559" xsd:float
-property_value: Formula "C 24 H 39 N 8 O 17 P 3 S 2" xsd:string
-property_value: MassAvg "868.66" xsd:float
-property_value: MassMono "868.108744" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: Unimod:281
-is_a: MOD:00861
-is_a: MOD:00905
-is_a: MOD:01862
-
-[Term]
-id: MOD:00312
-name: S-myristoyl-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-myristoyl-L-cysteine." [PubMed:10026218, PubMed:10080938, PubMed:8824274, RESID:AA0307, Unimod:45#C]
-synonym: "(R)-2-amino-3-(tetradecanoylsulfanyl)propanoic acid" EXACT RESID-systematic []
-synonym: "LIPID S-myristoyl cysteine" EXACT UniProt-feature []
-synonym: "Myristoyl" RELATED PSI-MS-label []
-synonym: "Myristoylation" RELATED Unimod-description []
-synonym: "S-(C14:1 aliphatic acyl)cysteine" EXACT PSI-MOD-alternate []
-synonym: "S-myristoyl-L-cysteine" EXACT RESID-name []
-synonym: "S-myristoylated L-cysteine" EXACT PSI-MOD-alternate []
-synonym: "SMyrCys" EXACT PSI-MOD-label []
-synonym: "tetradecanoate cysteine thioester" EXACT RESID-alternate []
-property_value: DiffAvg "210.36" xsd:float
-property_value: DiffFormula "C 14 H 26 N 0 O 1 S 0" xsd:string
-property_value: DiffMono "210.198365" xsd:float
-property_value: Formula "C 17 H 31 N 1 O 2 S 1" xsd:string
-property_value: MassAvg "313.50" xsd:float
-property_value: MassMono "313.207550" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: Unimod:45
-is_a: MOD:00655
-is_a: MOD:00905
-
-[Term]
-id: MOD:00313
-name: S-palmitoleyl-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-palmitoleyl-L-cysteine." [OMSSA:187, PubMed:8294460, RESID:AA0308, Unimod:431#C]
-synonym: "(R)-2-amino-3-((Z)-9-hexadecenoylsulfanyl)propanoic acid" EXACT RESID-systematic []
-synonym: "cis-9-hexadecenoate cysteine thioester" EXACT RESID-alternate []
-synonym: "mod187" EXACT OMSSA-label []
-synonym: "Palmitoleyl" RELATED PSI-MS-label []
-synonym: "palmitoleyl" RELATED Unimod-description []
-synonym: "S-palmitoleyl-L-cysteine" EXACT RESID-name []
-synonym: "S-palmitoleylated L-cysteine" EXACT PSI-MOD-alternate []
-synonym: "SPamD1Cys" EXACT PSI-MOD-label []
-property_value: DiffAvg "236.40" xsd:float
-property_value: DiffFormula "C 16 H 28 N 0 O 1 S 0" xsd:string
-property_value: DiffMono "236.214016" xsd:float
-property_value: Formula "C 19 H 33 N 1 O 2 S 1" xsd:string
-property_value: MassAvg "339.54" xsd:float
-property_value: MassMono "339.223200" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: Unimod:431
-xref: uniprot.ptm:PTM-0645
-is_a: MOD:02002
-is_a: MOD:00905
-
-[Term]
-id: MOD:00314
-name: glycine cholesterol ester
-def: "A protein modification that effectively converts a glycine residue to glycine cholesterol ester." [PubMed:11111088, PubMed:8824192, RESID:AA0309, Unimod:432#C-term, ChEBI:143135]
-comment: Incidental to RESID:AA0060. Unimod origin corrected [JSG].
-subset: PSI-MOD-slim
-synonym: "C-cholesterol" RELATED Unimod-interim []
-synonym: "cholesterol ester" RELATED Unimod-description []
-synonym: "cholesteryl glycinate" EXACT RESID-alternate []
-synonym: "glycine cholest-5-en-3beta-ol ester" EXACT RESID-systematic []
-synonym: "glycine cholesterol ester" EXACT RESID-name []
-synonym: "hedgehog lipophilic adduct" EXACT RESID-alternate []
-synonym: "LIPID Cholesterol glycine ester" EXACT UniProt-feature []
-property_value: DiffAvg "368.65" xsd:float
-property_value: DiffFormula "C 27 H 44 N 0 O 0" xsd:string
-property_value: DiffMono "368.344301" xsd:float
-property_value: Formula "C 29 H 48 N 1 O 2" xsd:string
-property_value: MassAvg "442.71" xsd:float
-property_value: MassMono "442.368505" xsd:float
-property_value: Origin "G" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: Unimod:432
-xref: uniprot.ptm:PTM-0090
-is_a: MOD:00908
-is_a: MOD:01155
-
-[Term]
-id: MOD:00315
-name: pentakis-L-cysteinyl L-histidino nickel tetrairon pentasulfide
-def: "A protein modification that effectively converts five L-cysteine residues, an L-histidine residue and a one-nickel four-iron five-sulfur cluster to pentakis-L-cysteinyl L-histidino nickel tetrairon pentasulfide." [PubMed:11509720, PubMed:2550436, RESID:AA0310]
-comment: Cross-link 6.
-synonym: "carbon monoxide dehydrogenase nickel-iron cofactor" EXACT RESID-alternate []
-synonym: "METAL Nickel-iron-sulfur (Ni-4Fe-5S)" EXACT UniProt-feature []
-synonym: "METAL Nickel-iron-sulfur (Ni-4Fe-5S); via tele nitrogen" EXACT UniProt-feature []
-synonym: "mu-1:2kappaS-sulfido-mu3-1:3:5kappaS-sulfido-mu3-2:3:4kappaS-sulfido-mu3-2:4:5kappaS-sulfido-mu3-3:4:5kappaS-sulfido-N1'-histidino-S-cysteinyl-1-iron-S-cysteinyl-2-nickel-3,4,5-tris-(S-cysteinyl iron)" EXACT RESID-systematic []
-synonym: "Ni-4Fe-5S cluster" EXACT RESID-alternate []
-synonym: "pentakis-L-cysteinyl L-histidino nickel tetrairon pentasulfide" EXACT RESID-name []
-property_value: DiffAvg "436.33" xsd:float
-property_value: DiffFormula "C 0 Fe 4 H -6 N 0 Ni 1 O 0 S 5" xsd:string
-property_value: DiffMono "435.488498" xsd:float
-property_value: Formula "C 21 Fe 4 H 26 N 8 Ni 1 O 6 S 10" xsd:string
-property_value: MassAvg "1089.16" xsd:float
-property_value: MassMono "1087.593333" xsd:float
-property_value: Origin "C, C, C, C, C, H" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00739
-is_a: MOD:00741
-is_a: MOD:02067
-is_a: MOD:02070
-
-[Term]
-id: MOD:00316
-name: N4,N4-dimethyl-L-asparagine
-def: "A protein modification that effectively converts an L-asparagine residue to N4,N4-dimethyl-L-asparagine." [PubMed:12964758, PubMed:14570711, PubMed:8783012, RESID:AA0311, Unimod:36#N]
-synonym: "(2S)-2-amino-4-(dimethylamino)-4-oxobutanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-N4,N4-dimethylbutanediamic acid" EXACT RESID-alternate []
-synonym: "beta-dimethylasparagine" RELATED RESID-misnomer []
-synonym: "di-Methylation" RELATED Unimod-description []
-synonym: "Dimethyl" RELATED PSI-MS-label []
-synonym: "MOD_RES N4,N4-dimethylasparagine" EXACT UniProt-feature []
-synonym: "N(gamma),N(gamma)-dimethylasparagine" EXACT RESID-alternate []
-synonym: "N4,N4-dimethyl-L-asparagine" EXACT RESID-name []
-synonym: "N4,N4-dimethylated L-asparagine" EXACT PSI-MOD-alternate []
-synonym: "N4Me2Asn" EXACT PSI-MOD-label []
-property_value: DiffAvg "28.05" xsd:float
-property_value: DiffFormula "C 2 H 4 N 0 O 0" xsd:string
-property_value: DiffMono "28.031300" xsd:float
-property_value: Formula "C 6 H 10 N 2 O 2" xsd:string
-property_value: MassAvg "142.16" xsd:float
-property_value: MassMono "142.074228" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: Unimod:36
-xref: uniprot.ptm:PTM-0182
-is_a: MOD:00429
-is_a: MOD:00602
-is_a: MOD:00673
-
-[Term]
-id: MOD:00317
-name: N6-3,4-didehydroretinylidene-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-3,4-didehydroretinylidene-L-lysine." [PubMed:10717661, PubMed:3257009, PubMed:4056688, RESID:AA0312, Unimod:433#K]
-synonym: "(S)-2-amino-6-[(2E,4E,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethylcyclohexa-1,3-dien-1-yl)-2,4,6,8-nonatetraenylidene]aminohexanoic acid" EXACT RESID-systematic []
-synonym: "3,4-didehydroretinylidene" RELATED Unimod-description []
-synonym: "Didehydroretinylidene" RELATED PSI-MS-label []
-synonym: "N6-(3,4-didehydroretinylidene)-L-lysine" EXACT RESID-name []
-synonym: "N6-3-dehydroretinal-L-lysine" EXACT RESID-alternate []
-synonym: "N6-3-dehydroretinyl-lysine" EXACT RESID-alternate []
-property_value: DiffAvg "264.41" xsd:float
-property_value: DiffFormula "C 20 H 24 N 0 O 0" xsd:string
-property_value: DiffMono "264.187801" xsd:float
-property_value: Formula "C 26 H 36 N 2 O 1" xsd:string
-property_value: MassAvg "392.59" xsd:float
-property_value: MassMono "392.282764" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:433
-is_a: MOD:00912
-
-[Term]
-id: MOD:00318
-name: 4'-(S-L-cysteinyl)-L-tryptophyl quinone
-def: "A protein modification that effectively cross-links an L-cysteine residue and an L-tryptophan residue by a thioether bond to form 4'-(S-L-cysteinyl)-L-tryptophyl quinone." [PubMed:11555656, PubMed:11717396, RESID:AA0313]
-comment: Cross-link 2; secondary to RESID:AA0148.
-synonym: "(2R)-2-amino-3-[(3-[(2S)-2-amino-2-carboxyethyl]-6,7-dioxo-6,7-dihydro-1H-indol-4-yl)sulfanyl]propanoic acid" EXACT RESID-systematic []
-synonym: "3-(2-amino-2-carboxyethyl)-4-[2-amino-2-carboxyethyl]sulfanyl-6,7-indolinedione" EXACT RESID-alternate []
-synonym: "4'-(L-cystein-S-yl)-L-tryptophyl quinone" EXACT RESID-name []
-synonym: "4-(S-cysteinyl)tryptophan-6,7-dione" EXACT RESID-alternate []
-synonym: "CROSSLNK 4'-cysteinyl-tryptophylquinone (Cys-Trp)" EXACT UniProt-feature []
-synonym: "CTQ" EXACT RESID-alternate []
-synonym: "cysteine tryptophylquinone" EXACT RESID-alternate []
-property_value: DiffAvg "27.97" xsd:float
-property_value: DiffFormula "C 0 H -4 N 0 O 2 S 0" xsd:string
-property_value: DiffMono "27.958529" xsd:float
-property_value: Formula "C 14 H 11 N 3 O 4 S 1" xsd:string
-property_value: MassAvg "317.32" xsd:float
-property_value: MassMono "317.047027" xsd:float
-property_value: Origin "C, W" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0041
-is_a: MOD:00687
-is_a: MOD:02057
-
-[Term]
-id: MOD:00319
-name: 3-(S-L-cysteinyl)-L-aspartic acid
-def: "A protein modification that effectively cross-links an L-cysteine residue and an L-aspartic acid residue by a thioether bond to form 2-(S-L-cysteinyl)-L-aspartic acid." [PubMed:11555656, PubMed:11717396, RESID:AA0314]
-comment: Cross-link 2.
-synonym: "(2R,3S)-2-amino-3-([(2R)-2-amino-2-carboxyethyl]sulfanyl)butanedioic acid" EXACT RESID-systematic []
-synonym: "(2R,3S,6R)-2,6-diamino-3-carboxy-4-thiaheptanedioic acid" EXACT RESID-alternate []
-synonym: "3-(L-cystein-S-yl)-L-aspartic acid" EXACT RESID-name []
-synonym: "3-carboxy-L-lanthionine" EXACT RESID-alternate []
-synonym: "CROSSLNK 3-cysteinyl-aspartic acid (Cys-Asp)" EXACT UniProt-feature []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 7 H 8 N 2 O 4 S 1" xsd:string
-property_value: MassAvg "216.21" xsd:float
-property_value: MassMono "216.020478" xsd:float
-property_value: Origin "C, D" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0025
-is_a: MOD:02043
-is_a: MOD:01993
-
-[Term]
-id: MOD:00320
-name: 4-(S-L-cysteinyl)-L-glutamic acid
-def: "A protein modification that effectively cross-links an L-cysteine residue and an L-glutamic acid residue by a thioether bond to form 4-(S-L-cysteinyl)-L-glutamic acid." [ChEBI:20293, PubMed:11555656, PubMed:11717396, RESID:AA0315]
-comment: Cross-link 2.
-synonym: "(2S,3S,7R)-2,7-diamino-4-carboxy-5-thiaoctanedioic acid" EXACT RESID-alternate []
-synonym: "(2S,4S)-2-amino-4-[(R)-2-amino-2-carboxyethyl]sulfanylpentanedioic acid" EXACT RESID-systematic []
-synonym: "4-(L-cystein-S-yl)-L-glutamic acid" EXACT RESID-name []
-synonym: "CROSSLNK 4-cysteinyl-glutamic acid (Cys-Glu)" EXACT UniProt-feature []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 8 H 10 N 2 O 4 S 1" xsd:string
-property_value: MassAvg "230.24" xsd:float
-property_value: MassMono "230.036128" xsd:float
-property_value: Origin "C, E" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0040
-is_a: MOD:00687
-is_a: MOD:02045
-
-[Term]
-id: MOD:00321
-name: cis-14-hydroxy-10,13-dioxo-7-heptadecenoic acid L-aspartate ester
-def: "A protein modification that effectively converts an L-aspartic acid residue to cis-14-hydroxy-10,13-dioxo-7-heptadecenoic acid L-aspartate ester." [PubMed:11435437, PubMed:7949339, RESID:AA0316, Unimod:434#D]
-synonym: "(7Z,14Xi)-14-[(S)-3-amino-3-carboxy-propanoyl]oxy-10,13-dioxo-7-heptadecenoic acid" EXACT RESID-systematic []
-synonym: "barley lipid transfer protein modification" EXACT RESID-alternate []
-synonym: "CHDH" RELATED PSI-MS-label []
-synonym: "cis-14-hydroxy-10,13-dioxo-7-heptadecenoic acid L-aspartate ester" EXACT RESID-name []
-synonym: "cis-14-hydroxy-10,13-dioxo-7-heptadecenoic ester" RELATED Unimod-description []
-synonym: "LIPID Cis-14-hydroxy-10,13-dioxo-7-heptadecenoic acid aspartate ester" EXACT UniProt-feature []
-property_value: DiffAvg "294.39" xsd:float
-property_value: DiffFormula "C 17 H 26 N 0 O 4" xsd:string
-property_value: DiffMono "294.183109" xsd:float
-property_value: Formula "C 21 H 31 N 1 O 7" xsd:string
-property_value: MassAvg "409.48" xsd:float
-property_value: MassMono "409.210052" xsd:float
-property_value: Origin "D" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:434
-xref: uniprot.ptm:PTM-0091
-is_a: MOD:00904
-is_a: MOD:01155
-
-[Term]
-id: MOD:00322
-name: 1'-methyl-L-histidine
-def: "A protein modification that effectively converts an L-histidine residue to tele-methyl-L-histidine." [PubMed:10601317, PubMed:11474090, PubMed:11875433, PubMed:6692818, PubMed:8076, PubMed:8645219, RESID:AA0317]
-subset: PSI-MOD-slim
-synonym: "(S)-2-amino-3-(1-methyl-1H-imidazol-4-yl)propanoic acid" EXACT RESID-systematic []
-synonym: "1'-methyl-L-histidine" EXACT RESID-name []
-synonym: "3-methylhistidine" RELATED RESID-misnomer []
-synonym: "4-methyl-histidine" RELATED RESID-misnomer []
-synonym: "Methyl" RELATED PSI-MS-label []
-synonym: "Methylation" RELATED Unimod-description []
-synonym: "MOD_RES Tele-methylhistidine" EXACT UniProt-feature []
-synonym: "N(epsilon)-methylhistidine" EXACT RESID-alternate []
-synonym: "N(tau)-methylhistidine" EXACT RESID-alternate []
-synonym: "NteleMeHis" EXACT PSI-MOD-label []
-synonym: "tele-methylated L-histidine" EXACT PSI-MOD-alternate []
-synonym: "tele-methylhistidine" EXACT RESID-alternate []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 7 H 9 N 3 O 1" xsd:string
-property_value: MassAvg "151.17" xsd:float
-property_value: MassMono "151.074562" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0290
-is_a: MOD:02038
-is_a: MOD:00724
-
-[Term]
-id: MOD:00323
-name: L-lysine methyl ester
-def: "A protein modification that effectively converts an L-lysine residue to L-lysine methyl ester." [PubMed:10973948, PubMed:11875433, RESID:AA0318, Unimod:34#C-term]
-subset: PSI-MOD-slim
-synonym: "2,6-diaminohexanoic methyl ester" EXACT RESID-alternate []
-synonym: "alpha,epsilon-diaminocaproic methyl ester" EXACT RESID-alternate []
-synonym: "L-lysine methyl ester" EXACT RESID-name []
-synonym: "Methyl" RELATED PSI-MS-label []
-synonym: "methyl (S)-2,6-diaminohexanoate" EXACT RESID-systematic []
-synonym: "methyl esterified L-lysine" EXACT PSI-MOD-alternate []
-synonym: "methyl L-lysinate" EXACT RESID-alternate []
-synonym: "Methylation" RELATED Unimod-description []
-synonym: "MOD_RES Lysine methyl ester" EXACT UniProt-feature []
-synonym: "OMeLys" EXACT PSI-MOD-label []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 7 H 15 N 2 O 2" xsd:string
-property_value: MassAvg "159.21" xsd:float
-property_value: MassMono "159.113353" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: Unimod:34
-xref: uniprot.ptm:PTM-0170
-is_a: MOD:01683
-is_a: MOD:01689
-
-[Term]
-id: MOD:00324
-name: L-serinyl molybdenum bis(molybdopterin guanine dinucleotide)
-def: "A protein modification that effectively converts an L-serine residue to L-serinyl molybdenum bis(molybdopterin guanine dinucleotide)." [PubMed:8658132, PubMed:8658134, RESID:AA0319]
-synonym: "2-amino-5,6-dimercapto-7-methyl-3,7,8a,9-tetrahydro-8-oxa-1,3,9,10-tetraazaanthracen-4-one guanosine dinucleotide" EXACT RESID-alternate []
-synonym: "bis[8-amino-1a,2,4a,5,6,7,10-heptahydro-2-(trihydrogen diphosphate 5'-ester with guanosine)methyl-6-oxo-3,4-disulfanyl-pteridino[6,7-5,6]pyranoato-S3,S4]-O3-serinyl-molybdenum oxide" EXACT RESID-systematic []
-synonym: "L-serinyl molybdenum bis(molybdopterin guanine dinucleotide)" EXACT RESID-name []
-property_value: DiffAvg "1588.01" xsd:float
-property_value: DiffFormula "C 40 H 47 Mo 1 N 20 O 27 P 4 S 4" xsd:string
-property_value: DiffMono "1588.980690" xsd:float
-property_value: Formula "C 43 H 52 Mo 1 N 21 O 29 P 4 S 4" xsd:string
-property_value: MassAvg "1675.09" xsd:float
-property_value: MassMono "1676.012718" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00744
-is_a: MOD:02072
-
-[Term]
-id: MOD:00325
-name: L-beta-methylthioasparagine
-def: "A protein modification that effectively converts an L-asparagine residue to L-beta-methylthioasparagine." [RESID:AA0320, Unimod:39#N]
-comment: This modification was predicted for ribosomal protein S12 in Bacillus subtilis when the sequence in the original version of the genome was reported to have asparagine rather than aspartic acid at the position of the methylthioaspartic acid modification (see MOD:00237). Two groups independently confirmed that the genome sequence was incorrect. The sequence in the revised genome has aspartic acid at that position. This is a deprecated entry in RESID. It probably does not occur naturally [JSG].
-synonym: "(2R,3Xi)-2-amino-3-(methylsulfanyl)-4-butanediamic acid" EXACT RESID-systematic []
-synonym: "2,4-diamino-3-(methylsulfanyl)-4-oxobutanoic acid" EXACT RESID-alternate []
-synonym: "3-(methylthio)-L-asparagine" EXACT RESID-name []
-synonym: "3-carboxamido-S-methyl-cysteine" EXACT RESID-alternate []
-synonym: "beta-(methylthio)asparagine" EXACT RESID-alternate []
-synonym: "Beta-methylthiolation" RELATED Unimod-description []
-synonym: "Methylthio" RELATED Unimod-interim []
-property_value: DiffAvg "46.09" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0 S 1" xsd:string
-property_value: DiffMono "45.987721" xsd:float
-property_value: Formula "C 5 H 8 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "160.19" xsd:float
-property_value: MassMono "160.030649" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: Unimod:39
-is_a: MOD:00903
-is_a: MOD:01153
-
-[Term]
-id: MOD:00326
-name: L-pyrrolysine (Lys)
-def: "A protein modification that effectively converts an L-lysine residue to L-pyrrolysine (not known as a natural, post-translational modification process)." [PubMed:11435424, PubMed:12029131, PubMed:12029132, PubMed:15314242, PubMed:16096277, RESID:AA0321#LYS, Unimod:435#K]
-comment: This entry is for the artifactual formation of L-pyrrolysine from lysine. For encoded L-pyrrolysine, use MOD:01187 [JSG].
-synonym: "(2S)-2-amino-6-[(2R,3R)-3-methyl-3,4-dihydro-2H-pyrrol-2-ylcarbonyl]aminohexanoic acid" EXACT RESID-systematic []
-synonym: "2-azanyl-6-[(2R,3R)-3-methyl-3,4-dihydro-2H-pyrrol-2-ylcarbonyl]azanylhexanoic acid" EXACT RESID-alternate []
-synonym: "L-pyrrolysine" EXACT RESID-name []
-synonym: "monomethylamine methyltransferase cofactor lysine adduct" EXACT RESID-alternate []
-synonym: "N6-(4-methyl-1,2-didehydropyrrolidine-5-carboxyl)-L-lysine" EXACT RESID-alternate []
-synonym: "N6-(4-methyl-delta-1-pyrroline-5-carboxyl)-L-lysine" EXACT RESID-alternate []
-synonym: "N6-([(2R,3R)-3-methyl-3,4-dihydro-2H-pyrrol-2-yl]carbonyl)-L-lysine" EXACT RESID-alternate []
-synonym: "NON_STD Pyrrolysine" EXACT UniProt-feature []
-synonym: "Pyl(Lys)" EXACT PSI-MOD-label []
-property_value: DiffAvg "109.13" xsd:float
-property_value: DiffFormula "C 6 H 7 N 1 O 1" xsd:string
-property_value: DiffMono "109.052764" xsd:float
-property_value: Formula "C 12 H 19 N 3 O 2" xsd:string
-property_value: MassAvg "237.30" xsd:float
-property_value: MassMono "237.147727" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:435
-is_a: MOD:00912
-
-[Term]
-id: MOD:00327
-name: 3-hydroxy-L-tryptophan
-def: "A protein modification that effectively converts an L-tryptophan residue to a 3-hydroxy-L-tryptophan." [PubMed:10024453, PubMed:11457355, RESID:AA0322, ChEBI:141794]
-synonym: "(2S,3S)-2-amino-3-hydroxy-3-(1H-indol-3-yl)propanoic acid" EXACT RESID-systematic []
-synonym: "3-hydroxy-L-tryptophan" EXACT RESID-name []
-synonym: "3-hydroxylated L-tryptophan" EXACT PSI-MOD-alternate []
-synonym: "3-hydroxytryptophan" EXACT RESID-alternate []
-synonym: "3HyTrp" EXACT PSI-MOD-label []
-synonym: "beta-hydroxytryptophan" EXACT RESID-alternate []
-synonym: "MOD_RES 3-hydroxytryptophan" EXACT UniProt-feature []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 11 H 10 N 2 O 2" xsd:string
-property_value: MassAvg "202.21" xsd:float
-property_value: MassMono "202.074228" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: uniprot.ptm:PTM-0031
-is_a: MOD:01622
-
-[Term]
-id: MOD:00328
-name: O4'-(phospho-3'-DNA)-L-tyrosine
-def: "A protein modification that effectively crosslinks an L-tyrosine residue and the 3'-end of DNA through a phosphodiester bond to form O4'-(phospho-3'-DNA)-L-tyrosine." [PubMed:2211714, RESID:AA0323]
-synonym: "(S)-2-amino-3-[4-(3'-deoxyribonucleic acid phosphonoxy)phenyl]propanoic acid" EXACT RESID-systematic []
-synonym: "ACT_SITE O-(3'-phospho-DNA)-tyrosine intermediate" EXACT UniProt-feature []
-synonym: "O4'-(phospho-3'-DNA)-L-tyrosine" EXACT RESID-name []
-synonym: "O4'-L-tyrosine 3'-DNA phosphodiester" EXACT RESID-alternate []
-property_value: Origin "Y" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00750
-is_a: MOD:00919
-
-[Term]
-id: MOD:00329
-name: hydroxyheme-L-glutamate ester
-def: "A protein modification that effectively results from forming an adduct between a glutamic acid residue and the porphyrin compound heme b, (7,12-diethenyl-3,8,13,17-tetramethylporphyrin-2,18-dipropanoato)iron." [PubMed:11139583, PubMed:11821421, PubMed:11980497, RESID:AA0324, Unimod:436#E]
-synonym: "5-hydroxymethyl protoporphyrin IX 5-glutamate ester" EXACT RESID-alternate []
-synonym: "[3-[(S)-(4-amino-4-carboxy)butanoyloxymethyl]-7,12-diethenyl-8,13,17-trimethyl-21H,23H-porphine-2,18-bis(2-carboxyethyl)-N21,N22,N23,N24]-ferrate" EXACT RESID-systematic []
-synonym: "BINDING Heme (covalent; via 1 link)" EXACT UniProt-feature []
-synonym: "cytochrome P450 CYP4A family heme cofactor" EXACT RESID-alternate []
-synonym: "Hydroxyheme" RELATED PSI-MS-label []
-synonym: "hydroxyheme" RELATED Unimod-description []
-synonym: "hydroxyheme-L-glutamate ester" EXACT RESID-name []
-property_value: DiffAvg "614.48" xsd:float
-property_value: DiffFormula "C 34 Fe 1 H 30 N 4 O 4" xsd:string
-property_value: DiffMono "614.161643" xsd:float
-property_value: Formula "C 39 Fe 1 H 37 N 5 O 7" xsd:string
-property_value: MassAvg "743.60" xsd:float
-property_value: MassMono "743.204236" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:436
-is_a: MOD:00699
-is_a: MOD:02068
-
-[Term]
-id: MOD:00330
-name: (phospho-5'-guanosine)-L-histidine
-def: "A protein modification that effectively converts an L-histidine residue to a (phospho-5'-guanosine)-L-histidine." [PubMed:10529169, PubMed:10869342, PubMed:7559521, RESID:AA0325, Unimod:413#H]
-synonym: "(2S)-2-amino-3-(1-(5'-adenosine phosphono)imidazol-4-yl)propanoic acid" EXACT RESID-systematic []
-synonym: "1'-(phospho-5'-guanosine)-L-histidine" EXACT RESID-name []
-synonym: "ACT_SITE GMP-histidine intermediate" EXACT UniProt-feature []
-synonym: "L-histidine 5'-guanosine phosphoramidester" EXACT RESID-alternate []
-synonym: "L-histidine monoanhydride with 5'-guanylic acid" EXACT RESID-alternate []
-synonym: "N(tau)-5'-guanylic-L-histidine" EXACT RESID-alternate []
-synonym: "N1'-guanylylated histidine" EXACT RESID-alternate []
-synonym: "phospho-guanosine" RELATED Unimod-description []
-synonym: "Phosphoguanosine" RELATED PSI-MS-label []
-synonym: "tele-5'-guanylic-L-histidine" EXACT RESID-alternate []
-property_value: DiffAvg "345.21" xsd:float
-property_value: DiffFormula "C 10 H 12 N 5 O 7 P 1" xsd:string
-property_value: DiffMono "345.047434" xsd:float
-property_value: Formula "C 16 H 19 N 8 O 8 P 1" xsd:string
-property_value: MassAvg "482.35" xsd:float
-property_value: MassMono "482.106346" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:413
-is_a: MOD:00909
-is_a: MOD:01163
-
-[Term]
-id: MOD:00331
-name: tetrakis-L-cysteinyl triiron tetrasulfide
-def: "A protein modification that effectively converts four L-cysteine residues and a three-iron four-sulfur cluster to tetrakis-L-cysteinyl triiron tetrasulfide." [PubMed:11592901, PubMed:11941493, PubMed:2511202, PubMed:6094558, RESID:AA0326]
-comment: Cross-link 4.
-synonym: "bis[bis-L-cysteinyl iron disulfido]iron" EXACT RESID-alternate []
-synonym: "di-mu-1:2kappaS-sulfido di-mu-2:3kappaS-sulfido iron bis(bis-S-cysteinyliron)" EXACT RESID-systematic []
-synonym: "tetra-mu-sulfido tetrakis-S-L-cysteinyl triiron" EXACT RESID-alternate []
-synonym: "tetrakis-L-cysteinyl linear [3Fe-4S] cluster" EXACT RESID-alternate []
-synonym: "tetrakis-L-cysteinyl triiron tetrasulfide" EXACT RESID-name []
-synonym: "tetrakis-L-cysteinyl triiron tetrasulfide D2 cluster" EXACT RESID-alternate []
-property_value: DiffAvg "291.74" xsd:float
-property_value: DiffFormula "C 0 Fe 3 H -4 N 0 O 0 S 4" xsd:string
-property_value: DiffMono "291.663442" xsd:float
-property_value: FormalCharge "3-" xsd:string
-property_value: Formula "C 12 Fe 3 H 16 N 4 O 4 S 8" xsd:string
-property_value: MassAvg "704.30" xsd:float
-property_value: MassMono "703.700181" xsd:float
-property_value: Origin "C, C, C, C" xsd:string
-property_value: Source "hypothetical" xsd:string
-is_a: MOD:00739
-is_a: MOD:02067
-
-[Term]
-id: MOD:00332
-name: omega-N-glucosyl-L-arginine
-def: "A protein modification that effectively converts an L-arginine residue to N4-glucosyl-arginine." [PubMed:15279557, PubMed:8521968, PubMed:9536051, RESID:AA0327, Unimod:41#R]
-synonym: "(2S)-2-amino-5-(beta-D-glucopyranosyl[imino(methylamino)methyl]amino)pentanoic acid" EXACT RESID-systematic []
-synonym: "Hex" RELATED PSI-MS-label []
-synonym: "Hexose" RELATED Unimod-description []
-synonym: "NG-beta-D-glucosylarginine" EXACT RESID-alternate []
-synonym: "omega-N-(beta-D-glucosyl)-L-arginine" EXACT RESID-alternate []
-synonym: "omega-N-glucosyl-L-arginine" EXACT RESID-name []
-synonym: "omega-N-glycosyl-L-arginine" EXACT RESID-alternate []
-synonym: "CARBOHYD N-linked (Glc) arginine" EXACT UniProt-feature []
-property_value: DiffAvg "162.14" xsd:float
-property_value: DiffFormula "C 6 H 10 N 0 O 5" xsd:string
-property_value: DiffMono "162.052823" xsd:float
-property_value: Formula "C 12 H 22 N 4 O 6" xsd:string
-property_value: MassAvg "318.33" xsd:float
-property_value: MassMono "318.153934" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:41
-xref: uniprot.ptm:PTM-0515
-is_a: MOD:00433
-is_a: MOD:01980
-
-[Term]
-id: MOD:00333
-name: (3-aminopropyl)(L-aspartyl-1-amino)phosphoryl-5'-adenosine
-def: "A protein modification that effectively converts an L-asparagine residue to (3-aminopropyl)(L-aspartyl-1-amino)phosphoryl-5'-adenosine." [PubMed:7559516, PubMed:7835418, PubMed:8183363, RESID:AA0328, Unimod:437#C-term]
-comment: Unimod origin shown as C-term [JSG].
-synonym: "(3-aminopropyl)(L-aspartyl-1-amino)phosphoryl-5'-adenosine" EXACT RESID-name []
-synonym: "(3-aminopropyl)(L-aspartyl-1-amino)phosphoryl-5-adenosine" RELATED Unimod-description []
-synonym: "5'-O-[(3-aminopropoxy)(L-aspart-1-ylamino)phosphoryl]adenosine" EXACT RESID-systematic []
-synonym: "9-(5'-O-[(3-aminopropoxy)(L-aspart-1-ylamino)phosphoryl]-beta-D-ribofuranosyl)adenine" EXACT RESID-alternate []
-synonym: "C-Asn-deriv" RELATED Unimod-interim []
-synonym: "microcin C7 asparagine modification" EXACT RESID-alternate []
-synonym: "MOD_RES Aspartic acid 1-[(3-aminopropyl)(5'-adenosyl)phosphono]amide" EXACT UniProt-feature []
-synonym: "N-(aspart-1-yl)-O-(3-aminopropyl)-O-(5'-adenosyl)phosphoramide" EXACT RESID-alternate []
-property_value: DiffAvg "386.30" xsd:float
-property_value: DiffFormula "C 13 H 19 N 6 O 6 P 1" xsd:string
-property_value: DiffMono "386.110369" xsd:float
-property_value: Formula "C 17 H 26 N 8 O 9 P 1" xsd:string
-property_value: MassAvg "517.42" xsd:float
-property_value: MassMono "517.156036" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: Unimod:437
-xref: uniprot.ptm:PTM-0335
-is_a: MOD:00701
-is_a: MOD:00903
-
-[Term]
-id: MOD:00334
-name: 1'-heme-L-histidine
-def: "A protein modification that effectively results from forming an adduct between the tele nitrogen of a histidine residue and the porphyrin compound heme b, (7,12-diethenyl-3,8,13,17-tetramethylporphyrin-2,18-dipropanoato)iron." [PubMed:12033922, PubMed:12121092, RESID:AA0329, Unimod:390#H]
-synonym: "(S)-[7-ethenyl-12-[1-((2-amino-2-carboxyethyl)-1H-imidazol-1-yl)ethyl]-3,8,13,17-tetramethyl-21H,23H-porphine-2,18-bis(2-carboxyethyl)-N21,N22,N23,N24]-ferrate" EXACT RESID-systematic []
-synonym: "1'-heme-L-histidine" EXACT RESID-name []
-synonym: "2-[1-(N1'-histidyl)ethyl]protoporphyrin IX" EXACT RESID-alternate []
-synonym: "BINDING Heme (covalent; via tele nitrogen)" EXACT UniProt-feature []
-synonym: "Heme" RELATED PSI-MS-label []
-synonym: "heme" RELATED Unimod-description []
-synonym: "N(epsilon)-histidyl heme" EXACT RESID-alternate []
-synonym: "N(tau)-histidyl heme" EXACT RESID-alternate []
-synonym: "N1'-histidyl heme" EXACT RESID-alternate []
-synonym: "tele-histidyl heme" EXACT RESID-alternate []
-property_value: DiffAvg "616.50" xsd:float
-property_value: DiffFormula "C 34 Fe 1 H 32 N 4 O 4" xsd:string
-property_value: DiffMono "616.177293" xsd:float
-property_value: Formula "C 40 Fe 1 H 39 N 7 O 5" xsd:string
-property_value: MassAvg "753.64" xsd:float
-property_value: MassMono "753.236205" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: Unimod:390
-is_a: MOD:00699
-is_a: MOD:02070
-
-[Term]
-id: MOD:00335
-name: (2S,3S,2'R)-3-methyllanthionine sulfoxide
-def: "A protein modification that effectively cross-links an L-cysteine residue and an L-threonine residue by a thioether bond to form (2S,3S,2'R)-3-methyllanthionine sulfoxide." [PubMed:7737178, PubMed:9219543, RESID:AA0330]
-comment: Cross-link 2.
-synonym: "(2S,3S,4Xi,6R)-2,6-diamino-3-methyl-4-oxo-4-thiaheptanedioic acid" EXACT RESID-alternate []
-synonym: "(2S,3S,SXi)-2-amino-3-([(R)-2-amino-2-carboxyethyl]sulfinyl)butanoic acid" EXACT RESID-systematic []
-synonym: "3-methyl-L-lanthionine S-oxide" EXACT RESID-alternate []
-synonym: "3-methyl-L-lanthionine sulfoxide" EXACT RESID-name []
-synonym: "CROSSLNK Beta-methyllanthionine sulfoxide (Thr-Cys)" EXACT UniProt-feature []
-synonym: "S-oxy-3-methyllanthionine" EXACT RESID-alternate []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 7 H 10 N 2 O 3 S 1" xsd:string
-property_value: MassAvg "202.23" xsd:float
-property_value: MassMono "202.041213" xsd:float
-property_value: Origin "C, T" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0069
-is_a: MOD:02056
-is_a: MOD:01993
-relationship: has_functional_parent MOD:01981
-
-[Term]
-id: MOD:00336
-name: tris-L-cysteinyl L-aspartato diiron disulfide
-def: "A protein modification that effectively converts three L-cysteine residues, an L-aspartic acid residue and a two-iron two-sulfur cluster to tris-L-cysteinyl L-aspartato diiron disulfide." [PubMed:10968624, PubMed:1312028, PubMed:7947772, RESID:AA0331]
-comment: Cross-link 4.
-synonym: "di-mu-sulfido(bis-S-cysteinyliron)(S-cysteinyl-O4-aspartatoiron)" EXACT RESID-systematic []
-synonym: "METAL Iron-sulfur (2Fe-2S)" EXACT UniProt-feature []
-synonym: "tris-L-cysteinyl L-aspartato diiron disulfide" EXACT RESID-name []
-property_value: DiffAvg "171.78" xsd:float
-property_value: DiffFormula "C 0 Fe 2 H -4 N 0 O 0 S 2" xsd:string
-property_value: DiffMono "171.783814" xsd:float
-property_value: FormalCharge "2-" xsd:string
-property_value: Formula "C 13 Fe 2 H 16 N 4 O 6 S 5" xsd:string
-property_value: MassAvg "596.28" xsd:float
-property_value: MassMono "595.838311" xsd:float
-property_value: Origin "C, C, C, D" xsd:string
-property_value: Source "hypothetical" xsd:string
-is_a: MOD:00739
-is_a: MOD:02066
-is_a: MOD:02067
-
-[Term]
-id: MOD:00337
-name: S-carbamoyl-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-carbamoyl-L-cysteine." [PubMed:12586941, PubMed:240389, RESID:AA0332, Unimod:5#C]
-synonym: "(R)-2-amino-3-(carbamoylsulfanyl)propanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-3-(aminocarbonyl)sulfanylpropanoic acid" EXACT RESID-alternate []
-synonym: "2-amino-3-(aminocarbonyl)thiopropanoic acid" EXACT RESID-alternate []
-synonym: "alpha-amino-beta-carbamylthiopropionic acid" EXACT RESID-alternate []
-synonym: "beta-carbamylthioalanine" EXACT RESID-alternate []
-synonym: "MOD_RES S-carbamoylcysteine" EXACT UniProt-feature []
-synonym: "S-(aminocarbonyl)cysteine" EXACT RESID-alternate []
-synonym: "S-carbamoyl-L-cysteine" EXACT RESID-name []
-synonym: "S-carbamoylcysteine" EXACT RESID-alternate []
-synonym: "S-carbamylcysteine" EXACT RESID-alternate []
-synonym: "S-cysteinyl carbamate ester" EXACT RESID-alternate []
-synonym: "SCbmCys" EXACT PSI-MOD-label []
-property_value: DiffAvg "43.02" xsd:float
-property_value: DiffFormula "C 1 H 1 N 1 O 1 S 0" xsd:string
-property_value: DiffMono "43.005814" xsd:float
-property_value: Formula "C 4 H 6 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "146.16" xsd:float
-property_value: MassMono "146.014998" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:5
-xref: uniprot.ptm:PTM-0649
-is_a: MOD:00398
-is_a: MOD:00905
-
-[Term]
-id: MOD:00338
-name: S-cyano-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-cyano-L-cysteine." [PubMed:12586941, PubMed:4808702, RESID:AA0333, Unimod:438#C]
-synonym: "(2R)-2-amino-3-thiocyanatopropanoic acid" EXACT RESID-systematic []
-synonym: "alpha-amino-beta-thiocyanatopropionic acid" EXACT RESID-alternate []
-synonym: "beta-thiocyanatoalanine" EXACT RESID-alternate []
-synonym: "Cyano" RELATED PSI-MS-label []
-synonym: "cyano" RELATED Unimod-description []
-synonym: "MOD_RES S-cyanocysteine" EXACT UniProt-feature []
-synonym: "S-cyano-L-cysteine" EXACT RESID-name []
-synonym: "S-cyanocysteine" EXACT RESID-alternate []
-synonym: "serine thiocyanic acid ester" EXACT RESID-alternate []
-property_value: DiffAvg "25.01" xsd:float
-property_value: DiffFormula "C 1 H -1 N 1 O 0 S 0" xsd:string
-property_value: DiffMono "24.995249" xsd:float
-property_value: Formula "C 4 H 4 N 2 O 1 S 1" xsd:string
-property_value: MassAvg "128.15" xsd:float
-property_value: MassMono "128.004434" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:438
-xref: uniprot.ptm:PTM-0650
-is_a: MOD:00893
-is_a: MOD:00905
-
-[Term]
-id: MOD:00339
-name: L-cysteinyl hydrogenase diiron subcluster
-def: "A protein modification that effectively converts an L-cysteine residue to L-cysteinyl hydrogenase diiron subcluster." [PubMed:10694885, PubMed:9836629, RESID:AA0334, Unimod:439#C]
-comment: incidental to RESID:AA0140.
-synonym: "1,7-biscarbonyl-1-(cystein-S-yl)-8-oxo-4-aza-2lambda(3),6 lambda(3)-dithia-1,7-diferratricyclo[4.2.0.0(2,7)]octane-1,7-dicarbonitrile" EXACT RESID-alternate []
-synonym: "Diironsubcluster" RELATED PSI-MS-label []
-synonym: "hydrogenase diiron subcluster" RELATED Unimod-description []
-synonym: "L-cysteinyl hydrogenase diiron subcluster" EXACT RESID-name []
-synonym: "METAL Diiron subcluster" EXACT UniProt-feature []
-synonym: "mu-carbonyl-dicarbonyl-1kappaC,2kappaC-dicyanido-1kappaC,2kappaC-cysteinato-1kS-1,2-azadimethanthiol-1kS,2kS'-diiron" EXACT RESID-systematic []
-property_value: DiffAvg "342.87" xsd:float
-property_value: DiffFormula "C 5 Fe 2 H -1 N 2 O 5 S 2" xsd:string
-property_value: DiffMono "342.786913" xsd:float
-property_value: Formula "C 8 Fe 2 H 4 N 3 O 6 S 3" xsd:string
-property_value: MassAvg "446.01" xsd:float
-property_value: MassMono "445.796098" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:439
-is_a: MOD:00738
-is_a: MOD:02067
-
-[Term]
-id: MOD:00340
-name: S-amidino-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-amidino-L-cysteine." [PubMed:9148748, RESID:AA0335, Unimod:440#C]
-synonym: "(2R)-2-amino-3-(carbamimidoylsulfanyl)propanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-3-amidinosulfanylpropanoic acid" EXACT RESID-alternate []
-synonym: "2-amino-3-amidinothiopropanoic acid" EXACT RESID-alternate []
-synonym: "ACT_SITE Amidino-cysteine intermediate" EXACT UniProt-feature []
-synonym: "alpha-amino-beta-amidinothiopropionic acid" EXACT RESID-alternate []
-synonym: "Amidino" RELATED PSI-MS-label []
-synonym: "amidino" RELATED Unimod-description []
-synonym: "beta-(S-isothiourea)alanine" EXACT RESID-alternate []
-synonym: "beta-amidinothioalanine" EXACT RESID-alternate []
-synonym: "S-amidino-L-cysteine" EXACT RESID-name []
-synonym: "S-amidinocysteine" EXACT RESID-alternate []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 1 H 2 N 2 O 0 S 0" xsd:string
-property_value: DiffMono "42.021798" xsd:float
-property_value: Formula "C 4 H 7 N 3 O 1 S 1" xsd:string
-property_value: MassAvg "145.18" xsd:float
-property_value: MassMono "145.030983" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:440
-is_a: MOD:00905
-
-[Term]
-id: MOD:00341
-name: N-methyl-L-isoleucine
-def: "A protein modification that effectively converts an L-isoleucine residue to N-methyl-L-isoleucine." [PubMed:11875433, RESID:AA0336]
-comment: Polypeptides with monomethylated amino terminals can undergo premature cleavage during the coupling step of an Edman degradation. This can result in \"preview\" with both a residue and the following residue being seen from the first step on through a sequence [JSG].
-synonym: "(2S,3S)-2-methylamino-3-methylpentanoic acid" EXACT RESID-systematic []
-synonym: "Methyl" RELATED PSI-MS-label []
-synonym: "Methylation" RELATED Unimod-description []
-synonym: "MOD_RES N-methylisoleucine" EXACT UniProt-feature []
-synonym: "N-methyl-L-isoleucine" EXACT RESID-name []
-synonym: "N-methylated L-isoleucine" EXACT PSI-MOD-alternate []
-synonym: "N-methylisoleucine" EXACT RESID-alternate []
-synonym: "NMe1Ile" EXACT PSI-MOD-label []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 7 H 13 N 1 O 1" xsd:string
-property_value: MassAvg "127.19" xsd:float
-property_value: MassMono "127.099714" xsd:float
-property_value: Origin "I" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: uniprot.ptm:PTM-0215
-is_a: MOD:00715
-is_a: MOD:01680
-
-[Term]
-id: MOD:00342
-name: N-methyl-L-leucine
-def: "A protein modification that effectively converts an L-leucine residue to N-methyl-L-leucine." [PubMed:11875433, RESID:AA0337]
-comment: Polypeptides with monomethylated amino terminals can undergo premature cleavage during the coupling step of an Edman degradation. This can result in \"preview\" with both a residue and the following residue being seen from the first step on through a sequence [JSG].
-synonym: "(S)-2-methylamino-4-methylpentanoic acid" EXACT RESID-systematic []
-synonym: "2-(methylamino)-4-methyl-valeric acid" EXACT RESID-alternate []
-synonym: "Methyl" RELATED PSI-MS-label []
-synonym: "Methylation" RELATED Unimod-description []
-synonym: "MOD_RES N-methylleucine" EXACT UniProt-feature []
-synonym: "N-methyl-L-leucine" EXACT RESID-name []
-synonym: "N-methylated L-leucine" EXACT PSI-MOD-alternate []
-synonym: "N-methylleucine" EXACT RESID-alternate []
-synonym: "NMe1Leu" EXACT PSI-MOD-label []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 7 H 13 N 1 O 1" xsd:string
-property_value: MassAvg "127.19" xsd:float
-property_value: MassMono "127.099714" xsd:float
-property_value: Origin "L" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: uniprot.ptm:PTM-0216
-is_a: MOD:01680
-is_a: MOD:01808
-
-[Term]
-id: MOD:00343
-name: N-methyl-L-tyrosine
-def: "A protein modification that effectively converts an L-tyrosine residue to N-methyl-L-tyrosine." [DeltaMass:0, RESID:AA0338]
-comment: Polypeptides with monomethylated amino terminals can undergo premature cleavage during the coupling step of an Edman degradation. This can result in \"preview\" with both a residue and the following residue being seen from the first step on through a sequence [JSG].
-synonym: "(2S)-3-(4-hydroxyphenyl)-2-(methylamino)propanoic acid" EXACT RESID-systematic []
-synonym: "Methyl" RELATED PSI-MS-label []
-synonym: "MOD_RES N-methyltyrosine" EXACT UniProt-feature []
-synonym: "N-methyl Tyrosinyl" EXACT DeltaMass-label []
-synonym: "N-methyl-L-tyrosine" EXACT RESID-name []
-synonym: "N-methylated L-tyrosine" EXACT PSI-MOD-alternate []
-synonym: "N-methyltyrosine" EXACT RESID-alternate []
-synonym: "NMe1Tyr" EXACT PSI-MOD-label []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 10 H 11 N 1 O 2" xsd:string
-property_value: MassAvg "177.20" xsd:float
-property_value: MassMono "177.078979" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: uniprot.ptm:PTM-0220
-is_a: MOD:00718
-is_a: MOD:01680
-
-[Term]
-id: MOD:00344
-name: N-palmitoylglycine
-def: "A protein modification that effectively converts a glycine residue to N-palmitoylglycine." [PubMed:12574119, RESID:AA0339]
-comment: incidental to RESID:AA0060
-subset: PSI-MOD-slim
-synonym: "(hexadecanamido)acetic acid" EXACT RESID-alternate []
-synonym: "(hexadecanoylamino)acetic acid" EXACT RESID-alternate []
-synonym: "(hexadecanoylamino)ethanoic acid" EXACT RESID-systematic []
-synonym: "LIPID N-palmitoyl glycine" EXACT UniProt-feature []
-synonym: "N-(1-oxohexadecyl)glycine" EXACT RESID-alternate []
-synonym: "N-palmitoyl-glycine" EXACT RESID-name []
-synonym: "N-palmitoylated glycine" EXACT PSI-MOD-alternate []
-synonym: "N-hexadecanoylated glycine" EXACT PSI-MOD-alternate []
-synonym: "NPamGly" EXACT PSI-MOD-label []
-property_value: DiffAvg "238.41" xsd:float
-property_value: DiffFormula "C 16 H 30 N 0 O 1 S 0" xsd:string
-property_value: DiffMono "238.229666" xsd:float
-property_value: Formula "C 18 H 34 N 1 O 2" xsd:string
-property_value: MassAvg "296.47" xsd:float
-property_value: MassMono "296.258954" xsd:float
-property_value: Origin "G" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0223
-is_a: MOD:00908
-is_a: MOD:01685
-
-[Term]
-id: MOD:00345
-name: 2-(S-L-cysteinyl)-L-phenylalanine
-def: "A protein modification that effectively cross-links an L-cysteine residue and an L-phenylalanine residue by a thioether bond to form 2-(S-L-cysteinyl)-L-phenylalanine." [PubMed:12696888, PubMed:3936839, RESID:AA0340]
-comment: Cross-link 2.
-synonym: "(2R)-2-amino-2-[(2R)-2-amino-2-carboxyethyl]sulfanyl-3-phenylpropanoic acid" EXACT RESID-systematic []
-synonym: "(2R,5R)-2,5-diamino-3-thia-2-phenylmethylhexanedioic acid" EXACT RESID-alternate []
-synonym: "2-(L-cystein-S-yl)-L-phenylalanine" EXACT RESID-name []
-synonym: "alpha-(L-cystein-S-yl)-L-phenylalanine" EXACT RESID-alternate []
-synonym: "CROSSLNK 2-cysteinyl-L-phenylalanine (Cys-Phe)" EXACT UniProt-feature []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 12 H 12 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "248.30" xsd:float
-property_value: MassMono "248.061949" xsd:float
-property_value: Origin "C, F" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0012
-is_a: MOD:02053
-is_a: MOD:01992
-
-[Term]
-id: MOD:00346
-name: 2-(S-L-cysteinyl)-D-phenylalanine
-def: "A protein modification that effectively cross-links an L-cysteine residue and an L-phenylalanine residue by a thioether bond to form 2-(S-L-cysteinyl)-D-phenylalanine." [PubMed:12696888, PubMed:3936839, RESID:AA0341]
-comment: Cross-link 2.
-synonym: "(2S)-2-amino-2-[(2R)-2-amino-2-carboxyethyl]sulfanyl-3-phenylpropanoic acid" EXACT RESID-systematic []
-synonym: "(2S,5R)-2,5-diamino-3-thia-2-phenylmethylhexanedioic acid" EXACT RESID-alternate []
-synonym: "2-(L-cystein-S-yl)-D-phenylalanine" EXACT RESID-name []
-synonym: "alpha-(L-cystein-S-yl)-D-phenylalanine" EXACT RESID-alternate []
-synonym: "CROSSLNK 2-cysteinyl-D-phenylalanine (Cys-Phe)" EXACT UniProt-feature []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 12 H 12 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "248.30" xsd:float
-property_value: MassMono "248.061949" xsd:float
-property_value: Origin "C, F" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0011
-is_a: MOD:00664
-is_a: MOD:02053
-is_a: MOD:01992
-
-[Term]
-id: MOD:00347
-name: 2-(S-L-cysteinyl)-D-allo-threonine
-def: "A protein modification that effectively cross-links an L-cysteine residue and an L-threonine residue by a thioether bond to form 2-(S-L-cysteinyl)-D-allo-threonine." [PubMed:12696888, PubMed:3936839, RESID:AA0342]
-comment: Cross-link 2.
-synonym: "(2R,5S,6R)-2,5-diamino-5-carboxy-6-hydroxy-4-thiaheptanoic acid" EXACT RESID-alternate []
-synonym: "(2S,3R)-2-amino-2-[(2R)-2-amino-2-carboxyethyl]sulfanyl-3-hydroxybutanoic acid" EXACT RESID-systematic []
-synonym: "2-(L-cystein-S-yl)-D-allo-threonine" EXACT RESID-name []
-synonym: "alpha-(L-cystein-S-yl)-D-allo-threonine" EXACT RESID-alternate []
-synonym: "CROSSLNK 2-cysteinyl-D-allo-threonine (Cys-Thr)" EXACT UniProt-feature []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 7 H 10 N 2 O 3 S 1" xsd:string
-property_value: MassAvg "202.23" xsd:float
-property_value: MassMono "202.041213" xsd:float
-property_value: Origin "C, T" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0010
-is_a: MOD:00664
-is_a: MOD:02056
-is_a: MOD:01992
-
-[Term]
-id: MOD:00348
-name: N-carbamoyl-L-alanine
-def: "A protein modification that effectively converts an L-alanine residue to N-carbamoyl-L-alanine." [PubMed:12203680, RESID:AA0343]
-synonym: "(S)-2-(carbamoylamino)propanoic acid" EXACT RESID-systematic []
-synonym: "2-ureidopropanoic acid" EXACT RESID-alternate []
-synonym: "MOD_RES N-carbamoylalanine" EXACT UniProt-feature []
-synonym: "N-carbamoyl-L-alanine" EXACT RESID-name []
-synonym: "N-carbamylalanine" EXACT RESID-alternate []
-synonym: "N2CbmAla" EXACT PSI-MOD-label []
-property_value: DiffAvg "43.02" xsd:float
-property_value: DiffFormula "C 1 H 1 N 1 O 1" xsd:string
-property_value: DiffMono "43.005814" xsd:float
-property_value: Formula "C 4 H 7 N 2 O 2" xsd:string
-property_value: MassAvg "115.11" xsd:float
-property_value: MassMono "115.050752" xsd:float
-property_value: Origin "A" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0374
-is_a: MOD:00901
-is_a: MOD:01679
-
-[Term]
-id: MOD:00349
-name: 4-amino-3-isothiazolidinone-L-serine
-def: "A protein modification that effectively crosslinks an L-cysteine residue and an L-serine residue to form 4-amino-3-isothiazolidinone-L-serine." [PubMed:12802338, PubMed:12802339, RESID:AA0344]
-comment: Cross-link 2.
-synonym: "(2S)-2-[(4R)-4-amino-3-oxo-1,2-thiazolidin-2-yl]-3-hydroxypropanoic acid" EXACT RESID-systematic []
-synonym: "2-(4-amino-3-oxo-isothiazolidin-2-yl)-3-hydroxy-propanoic acid" EXACT RESID-alternate []
-synonym: "4-amino-3-isothiazolidinone-L-serine" EXACT RESID-alternate []
-synonym: "CROSSLNK N,N-(cysteine-1,S-diyl)serine (Cys-Ser)" EXACT UniProt-feature []
-synonym: "N,N-(L-cysteine-1,S-diyl)-L-serine" EXACT RESID-name []
-synonym: "serine-cysteine sulfenyl amide cross-link" EXACT RESID-alternate []
-synonym: "serine-cysteine sulphenyl amide cross-link" EXACT RESID-alternate []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 6 H 8 N 2 O 3 S 1" xsd:string
-property_value: MassAvg "188.20" xsd:float
-property_value: MassMono "188.025563" xsd:float
-property_value: Origin "C, S" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0037
-is_a: MOD:02044
-is_a: MOD:02055
-is_a: MOD:01861
-
-[Term]
-id: MOD:00350
-name: L-threonyl-pentaglycyl-murein peptidoglycan
-def: "A protein modification that effectively attaches an L-threonine residue to murein peptidoglycan by a pentaglycine linker peptide." [PubMed:10754567, PubMed:1638631, RESID:AA0345]
-synonym: "(2R,6S)-2-(N-mureinyl-(R)-alanyl-(S)-isoglutamyl)amino-6-(threonyl-pentaglycyl)amino-pimeloyl-(S)-alanyl-(S)-alanine" EXACT RESID-alternate []
-synonym: "L-threonyl-pentaglycyl-murein peptidoglycan" EXACT RESID-name []
-synonym: "MOD_RES Pentaglycyl murein peptidoglycan amidated threonine" EXACT UniProt-feature []
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0246
-is_a: MOD:00917
-is_a: MOD:01159
-
-[Term]
-id: MOD:00351
-name: N-glycyl-1-(phosphatidyl)ethanolamine
-def: "A protein modification that effectively converts a glycine residue to N-glycyl-1-(phosphatidyl)ethanolamine." [PubMed:11100732, RESID:AA0346]
-synonym: "(R)-1-hexadecanoyloxy-2-((Z)-9-octadecenoyloxy)-3-[2-(aminoacetylamino)ethyloxyphospho]propane" EXACT RESID-systematic []
-synonym: "LIPID Phosphatidylethanolamine amidated glycine" EXACT UniProt-feature []
-synonym: "N-glycyl-1-(phosphatidyl)ethanolamine" EXACT RESID-name []
-synonym: "N-glycyl-1-palmitoyl-2-oleoyl-sn-glycero-3-phosphoethanolamine" EXACT RESID-alternate []
-property_value: DiffAvg "699.99" xsd:float
-property_value: DiffFormula "C 39 H 74 N 1 O 7 P 1" xsd:string
-property_value: DiffMono "699.520290" xsd:float
-property_value: Formula "C 41 H 78 N 2 O 9 P 1" xsd:string
-property_value: MassAvg "774.05" xsd:float
-property_value: MassMono "773.544494" xsd:float
-property_value: Origin "G" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0249
-is_a: MOD:00908
-is_a: MOD:01155
-
-[Term]
-id: MOD:00352
-name: L-glutamyl 5-omega-hydroxyceramide ester
-def: "A protein modification that effectively converts an L-glutamic acid residue to L-glutamyl 5-omega-hydroxyceramide ester." [PubMed:10411887, PubMed:9651377, RESID:AA0347]
-synonym: "(S)-2-amino-5-[30-((2S,3R,4E)-1,3-dihydroxyicos-4-en-2-ylamino)-30-oxotriacontan-1-yloxy]-5-oxopentanoic acid" EXACT RESID-systematic []
-synonym: "2-[30-(isoglutamyloxy)triacontanoyl]icosasphingosine" EXACT RESID-alternate []
-synonym: "L-glutamyl 5-omega-hydroxyceramide ester" EXACT RESID-name []
-synonym: "LIPID Omega-hydroxyceramide glutamate ester" EXACT UniProt-feature []
-property_value: DiffAvg "761.31" xsd:float
-property_value: DiffFormula "C 50 H 96 N 0 O 4" xsd:string
-property_value: DiffMono "760.730862" xsd:float
-property_value: Formula "C 55 H 104 N 2 O 6" xsd:string
-property_value: MassAvg "889.44" xsd:float
-property_value: MassMono "888.789439" xsd:float
-property_value: Origin "Q" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0236
-is_a: MOD:00907
-is_a: MOD:01155
-
-[Term]
-id: MOD:00353
-name: S-[5'-(L-tryptoph-6'-yl)-L-tyrosin-3'-yl]-L-methionin-S-ium
-def: "A protein modification that effectively cross-links an L-tryptophan residue with an L-tyrosine residue by a carbon-carbon bond, and cross-links the L-tyrosine residue to an L-methionine residue by a thioether bond to form S-[5'-(L-tryptoph-6'-yl)-L-tyrosin-3'-yl]-L-methionin-S-ium." [PubMed:12172540, PubMed:16285713, RESID:AA0348]
-comment: Cross-link 3.
-synonym: "5'-(6'-tryptophyl)-tyrosin-3'-yl-methionin-S-ium" EXACT RESID-alternate []
-synonym: "S-[5'-(L-tryptoph-6'-yl)-L-tyrosin-3'-yl]-L-methionin-S-ium" EXACT RESID-name []
-property_value: DiffAvg "-3.02" xsd:float
-property_value: DiffFormula "C 0 H -3 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "-3.024024" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 25 H 25 N 4 O 4 S 1" xsd:string
-property_value: MassAvg "477.56" xsd:float
-property_value: MassMono "477.159103" xsd:float
-property_value: Origin "M, W, Y" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0328
-is_a: MOD:00692
-is_a: MOD:02052
-is_a: MOD:02057
-is_a: MOD:02058
-
-[Term]
-id: MOD:00354
-name: O-(riboflavin phosphoryl)-L-threonine
-def: "A protein modification that effectively converts an L-threonine residue to O-(riboflavin phosphoryl)-L-threonine." [PubMed:10587447, PubMed:11163785, PubMed:11248234, RESID:AA0349, Unimod:442#T]
-subset: PSI-MOD-slim
-synonym: "(2S,3R)-2-amino-3-(riboflavin 5'-hydrogen phosphonoxy)butanoic acid" EXACT RESID-systematic []
-synonym: "FMN" RELATED PSI-MS-label []
-synonym: "MOD_RES FMN phosphoryl threonine" EXACT UniProt-feature []
-synonym: "O-(riboflavin phosphoryl)-L-threonine" EXACT RESID-name []
-synonym: "O3-(riboflavin phosphoryl)" RELATED Unimod-description []
-synonym: "O3-threonyl flavin mononucleotide" EXACT RESID-alternate []
-synonym: "O3-threonyl FMN" EXACT RESID-alternate []
-synonym: "OFMNThr" EXACT PSI-MOD-label []
-property_value: DiffAvg "438.33" xsd:float
-property_value: DiffFormula "C 17 H 19 N 4 O 8 P 1" xsd:string
-property_value: DiffMono "438.094050" xsd:float
-property_value: Formula "C 21 H 26 N 5 O 10 P 1" xsd:string
-property_value: MassAvg "539.44" xsd:float
-property_value: MassMono "539.141729" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:442
-xref: uniprot.ptm:PTM-0126
-is_a: MOD:00917
-is_a: MOD:01164
-
-[Term]
-id: MOD:00355
-name: O-(riboflavin phosphoryl)-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O-(riboflavin phosphoryl)-L-serine." [RESID:AA0350, Unimod:442#S]
-subset: PSI-MOD-slim
-synonym: "(R)-2-amino-3-(riboflavin 5'-hydrogen phosphonoxy)propanoic acid" EXACT RESID-systematic []
-synonym: "FMN" RELATED PSI-MS-label []
-synonym: "MOD_RES FMN phosphoryl serine" EXACT UniProt-feature []
-synonym: "O-(riboflavin phosphoryl)-L-serine" EXACT RESID-name []
-synonym: "O3-(riboflavin phosphoryl)" RELATED Unimod-description []
-synonym: "O3-seryl flavin mononucleotide" EXACT RESID-alternate []
-synonym: "O3-seryl FMN" EXACT RESID-alternate []
-synonym: "OFMNSer" EXACT PSI-MOD-label []
-property_value: DiffAvg "438.33" xsd:float
-property_value: DiffFormula "C 17 H 19 N 4 O 8 P 1" xsd:string
-property_value: DiffMono "438.094050" xsd:float
-property_value: Formula "C 20 H 24 N 5 O 10 P 1" xsd:string
-property_value: MassAvg "525.41" xsd:float
-property_value: MassMono "525.126079" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:442
-xref: uniprot.ptm:PTM-0125
-is_a: MOD:00916
-is_a: MOD:01164
-
-[Term]
-id: MOD:00356
-name: S-(4alpha-FMN)-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-(4a-FMN)-L-cysteine." [PubMed:12668455, PubMed:12846567, PubMed:7692961, RESID:AA0351, Unimod:443#C]
-subset: PSI-MOD-slim
-synonym: "(R)-2-amino-3-(4a-riboflavin 5'-dihydrogen phosphate)sulfanylpropanoic acid" EXACT RESID-systematic []
-synonym: "4a-(S-cysteinyl)flavin mononucleotide" EXACT RESID-alternate []
-synonym: "4a-(S-cysteinyl)FMN" EXACT RESID-alternate []
-synonym: "FMNC" RELATED PSI-MS-label []
-synonym: "MOD_RES S-4a-FMN cysteine" EXACT UniProt-feature []
-synonym: "S-(4a-FMN)" RELATED Unimod-description []
-synonym: "S-(4a-FMN)-L-cysteine" EXACT RESID-name []
-synonym: "S4aFMNCys" EXACT PSI-MOD-label []
-property_value: DiffAvg "456.35" xsd:float
-property_value: DiffFormula "C 17 H 21 N 4 O 9 P 1 S 0" xsd:string
-property_value: DiffMono "456.104615" xsd:float
-property_value: Formula "C 20 H 26 N 5 O 10 P 1 S 1" xsd:string
-property_value: MassAvg "559.49" xsd:float
-property_value: MassMono "559.113800" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:443
-xref: uniprot.ptm:PTM-0270
-is_a: MOD:02083
-is_a: MOD:00905
-
-[Term]
-id: MOD:00357
-name: 1'-(8alpha-FMN)-L-histidine
-def: "A protein modification that effectively converts an L-histidine residue to 1'-(8alpha-FMN)-L-histidine." [PubMed:11902668, PubMed:8611516, RESID:AA0352, Unimod:409#H]
-subset: PSI-MOD-slim
-synonym: "(S)-2-amino-3-(1-[8alpha riboflavin 5'-dihydrogen phosphate]imidazol-4-yl)propanoic acid" EXACT RESID-systematic []
-synonym: "1'-(8alpha-FMN)-L-histidine" EXACT RESID-name []
-synonym: "8alpha-(N(epsilon)-histidyl)FMN" EXACT RESID-alternate []
-synonym: "8alpha-(N1'-histidyl)FMN" EXACT RESID-alternate []
-synonym: "flavin mononucleotide" RELATED Unimod-description []
-synonym: "FMNH" RELATED PSI-MS-label []
-synonym: "MOD_RES Tele-8alpha-FMN histidine" EXACT UniProt-feature []
-synonym: "N(tau)-(8alpha-FMN)-histidine" EXACT RESID-alternate []
-synonym: "Ntele8aFMNHis" EXACT PSI-MOD-label []
-synonym: "tele-(8alpha-FMN)-histidine" EXACT RESID-alternate []
-property_value: DiffAvg "454.33" xsd:float
-property_value: DiffFormula "C 17 H 19 N 4 O 9 P 1" xsd:string
-property_value: DiffMono "454.088965" xsd:float
-property_value: Formula "C 23 H 26 N 7 O 10 P 1" xsd:string
-property_value: MassAvg "591.47" xsd:float
-property_value: MassMono "591.147877" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:409
-xref: uniprot.ptm:PTM-0289
-is_a: MOD:02085
-is_a: MOD:00909
-
-[Term]
-id: MOD:00358
-name: 3'-(8alpha-FMN)-L-histidine
-def: "A protein modification that effectively converts an L-histidine residue to 3'-(8alpha-FMN)-L-histidine." [PubMed:12417325, RESID:AA0353, Unimod:409#H]
-comment: In a later publication, PubMed:19438211, the authors changed the enzyme activity, the connection from a histidine nitrogen to a cysteine sulfur, and the identity of the flavin from FMN to FAD. They now believe the modification is S-(8alpha-FAD)-L-cysteine, see MOD:00152. This is a deprecated entry in RESID. It probably does not occur naturally [JSG].
-subset: PSI-MOD-slim
-synonym: "(S)-2-amino-3-(3-[8alpha riboflavin 5'-dihydrogen phosphate]imidazol-4-yl)propanoic acid" EXACT RESID-systematic []
-synonym: "3'-(8alpha-FMN)-L-histidine" EXACT RESID-name []
-synonym: "8alpha-(N(delta)-histidyl)FMN" EXACT RESID-alternate []
-synonym: "8alpha-(N3'-histidyl)FMN" EXACT RESID-alternate []
-synonym: "flavin mononucleotide" RELATED Unimod-description []
-synonym: "FMNH" RELATED PSI-MS-label []
-synonym: "N(pi)-(8alpha-FMN)-histidine" EXACT RESID-alternate []
-synonym: "Npros8aFMNHis" EXACT PSI-MOD-label []
-synonym: "pros-(8alpha-FMN)-histidine" EXACT RESID-alternate []
-property_value: DiffAvg "454.33" xsd:float
-property_value: DiffFormula "C 17 H 19 N 4 O 9 P 1" xsd:string
-property_value: DiffMono "454.088965" xsd:float
-property_value: Formula "C 23 H 26 N 7 O 10 P 1" xsd:string
-property_value: MassAvg "591.47" xsd:float
-property_value: MassMono "591.147877" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: Unimod:409
-is_a: MOD:02085
-is_a: MOD:00909
-
-[Term]
-id: MOD:00359
-name: N2-acetyl-L-arginine
-def: "A protein modification that effectively converts an L-arginine residue to N2-acetyl-L-arginine." [PubMed:12883043, PubMed:1894641, RESID:AA0354]
-synonym: "(S)-2-acetamido-5-carbamimidamidopentanoic acid" EXACT RESID-systematic []
-synonym: "2-acetamido-5-guanidinopentanoic acid" EXACT RESID-alternate []
-synonym: "2-acetylamino-5-guanidinopentanoic acid" EXACT RESID-alternate []
-synonym: "AcArg" EXACT PSI-MOD-label []
-synonym: "acetylarginine" EXACT RESID-alternate []
-synonym: "alpha-acetylamino-delta-guanidinovaleric acid" EXACT RESID-alternate []
-synonym: "MOD_RES N2-acetylarginine" EXACT UniProt-feature []
-synonym: "N(alpha)-acetylarginine" EXACT RESID-alternate []
-synonym: "N2-acetyl-L-arginine" EXACT RESID-name []
-synonym: "N2-acetylated L-arginine" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 2 H 2 N 0 O 1" xsd:string
-property_value: DiffMono "42.010565" xsd:float
-property_value: Formula "C 8 H 15 N 4 O 2" xsd:string
-property_value: MassAvg "199.23" xsd:float
-property_value: MassMono "199.119501" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0180
-is_a: MOD:00902
-is_a: MOD:01458
-
-[Term]
-id: MOD:00360
-name: L-cysteinyl copper sulfido molybdopterin cytosine dinuncleotide
-def: "A protein modification that effectively converts an L-cysteine residue to L-cysteinyl copper sulfido molybdopterin cytosine dinuncleotide." [PubMed:12475995, RESID:AA0355, Unimod:444#C]
-synonym: "[8-amino-1a,2,4a,5,6,7,10-heptahydro-2-(trihydrogen diphosphate 5'-ester with cytosine)methyl-6-oxo-3,4-dimercapto-pteridino[6,7-5,6]pyranoato-S3,S4]-cysteinyl-S-copper-mu-sulfido-molybdenum hydroxide oxide" EXACT RESID-systematic []
-synonym: "copper sulfido molybdopterin cytosine dinuncleotide" RELATED Unimod-description []
-synonym: "CuSMo" RELATED PSI-MS-label []
-synonym: "cysteinyl copper mu-sulfido Mo-pterin cytosine dinucleotide" EXACT RESID-alternate []
-synonym: "L-cysteinyl copper sulfido molybdopterin cytosine dinucleotide" EXACT RESID-name []
-property_value: DiffAvg "922.07" xsd:float
-property_value: DiffFormula "C 19 Cu 1 H 24 Mo 1 N 8 O 15 P 2 S 3" xsd:string
-property_value: DiffMono "922.834854" xsd:float
-property_value: Formula "C 22 Cu 1 H 29 Mo 1 N 9 O 16 P 2 S 4" xsd:string
-property_value: MassAvg "1025.20" xsd:float
-property_value: MassMono "1025.844039" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:444
-is_a: MOD:00742
-is_a: MOD:00744
-is_a: MOD:00860
-is_a: MOD:02067
-
-[Term]
-id: MOD:00361
-name: tris-L-cysteinyl S-adenosylmethion-N,O-diyl tetrairon tetrasulfide
-def: "A protein modification that effectively converts three L-cysteine residues, an S-adenosylmethionine and a four-iron four-sulfur cluster to tris-L-cysteinyl S-adenosylmethion-N,O-diyl tetrairon tetrasulfide." [PubMed:11222759, PubMed:14704425, RESID:AA0356]
-comment: Cross-link 3.
-synonym: "METAL Iron-sulfur (4Fe-4S-S-AdoMet)" EXACT UniProt-feature []
-synonym: "tetra-mu3-sulfido(S-adenosylmethion-N,O-diyliron)tris(S-cysteinyliron)" EXACT RESID-systematic []
-synonym: "tris-L-cysteinyl S-adenosylmethion-N,O-diyl tetrairon tetrasulfide" EXACT RESID-name []
-property_value: DiffAvg "747.03" xsd:float
-property_value: DiffFormula "C 15 Fe 4 H 19 N 6 O 5 S 5" xsd:string
-property_value: DiffMono "746.742346" xsd:float
-property_value: FormalCharge "1-" xsd:string
-property_value: Formula "C 24 Fe 4 H 34 N 9 O 8 S 8" xsd:string
-property_value: MassAvg "1056.45" xsd:float
-property_value: MassMono "1055.769901" xsd:float
-property_value: Origin "C, C, C" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00739
-is_a: MOD:02067
-
-[Term]
-id: MOD:00362
-name: tris-L-cysteinyl L-arginyl diiron disulfide
-def: "A protein modification that effectively converts three L-cysteine residues, an L-arginine residue and a two-iron two-sulfur cluster to tris-L-cysteinyl L-arginyl diiron disulfide." [PubMed:14704425, RESID:AA0357]
-comment: Cross-link 4.
-synonym: "di-mu-sulfido(N(eta1)-arginyl-S-cysteinyliron)(bis-S-cysteinyliron)" EXACT RESID-systematic []
-synonym: "METAL Iron-sulfur (2Fe-2S)" EXACT UniProt-feature []
-synonym: "tris-L-cysteinyl L-arginyl diiron disulfide" EXACT RESID-name []
-property_value: DiffAvg "172.79" xsd:float
-property_value: DiffFormula "C 0 Fe 2 H -3 N 0 O 0 S 2" xsd:string
-property_value: DiffMono "172.791639" xsd:float
-property_value: FormalCharge "2-" xsd:string
-property_value: Formula "C 15 Fe 2 H 24 N 7 O 4 S 5" xsd:string
-property_value: MassAvg "638.39" xsd:float
-property_value: MassMono "637.920304" xsd:float
-property_value: Origin "C, C, C, R" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00739
-is_a: MOD:02076
-is_a: MOD:02067
-
-[Term]
-id: MOD:00363
-name: L-cysteinyl-L-selenocysteine (Cys-Sec)
-def: "A protein modification that effectively cross-links an L-cysteine residue and an L-selenocysteine residues to form L-cysteinyl-L-selenocystine." [PubMed:12911312, RESID:AA0358#SEC]
-comment: Cross-link 2.
-subset: PSI-MOD-slim
-synonym: "(R,R)-2-amino-3-[3-(2-aminopropanoic acid)sulfanyl]selanylpropanoic acid" EXACT RESID-systematic []
-synonym: "CROSSLNK Cysteinyl-selenocysteine (Cys-Sec)" EXACT UniProt-feature []
-synonym: "CROSSLNK Cysteinyl-selenocysteine (Sec-Cys)" EXACT UniProt-feature []
-synonym: "L-cysteinyl-L-selenocysteine" EXACT RESID-name []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0 S 0 Se 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 6 H 8 N 2 O 2 S 1 Se 1" xsd:string
-property_value: MassAvg "251.17" xsd:float
-property_value: MassMono "251.947170" xsd:float
-property_value: Origin "C, U" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0109
-is_a: MOD:02061
-is_a: MOD:01627
-
-[Term]
-id: MOD:00364
-name: 5-hydroxy-N6,N6,N6-trimethyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to 5-hydroxy-N6,N6,N6-trimethyl-L-lysine." [PubMed:11349130, PubMed:14661085, RESID:AA0359, Unimod:445#K]
-comment: Incidental to RESID:AA0278; secondary to RESID:AA0028; secondary to RESID:AA0074.
-synonym: "(2R,5Xi)-5-amino-5-carboxy-2-hydroxy-N,N,N-trimethylpentan-1-aminium" EXACT RESID-systematic []
-synonym: "(2Xi,5S)-5-amino-5-carboxy-2-hydroxy-N,N,N-trimethylpentanaminium" EXACT RESID-alternate []
-synonym: "(2Xi,5S)-5-azanyl-5-carboxy-2-hydroxy-N,N,N-trimethylpentanazanium" EXACT RESID-alternate []
-synonym: "5-hydroxy-N(zeta)-trimethyllysine" EXACT RESID-alternate []
-synonym: "5-hydroxy-N6,N6,N6-trimethyl" RELATED Unimod-description []
-synonym: "5-hydroxy-N6,N6,N6-trimethyl-L-lysine" EXACT RESID-name []
-synonym: "5-hydroxy-N6,N6,N6-trimethyllysin-N6-ium" EXACT RESID-alternate []
-synonym: "5-hydroxy-N6,N6,N6-trimethyllysine cation" EXACT RESID-alternate []
-synonym: "5-hydroxylated N6,N6,N6-trimethylated L-lysine" EXACT PSI-MOD-alternate []
-synonym: "5HyN6Me3Lys" EXACT PSI-MOD-label []
-synonym: "alpha-amino-epsilon-dimethylamino-delta-hydroxycaproic acid" EXACT RESID-alternate []
-synonym: "delta-hydroxy-epsilon-N,N,N-trimethyllysine" EXACT RESID-alternate []
-synonym: "Hydroxytrimethyl" RELATED PSI-MS-label []
-synonym: "lysine derivative Lys(z)" EXACT RESID-alternate []
-synonym: "MOD_RES N6,N6,N6-trimethyl-5-hydroxylysine" EXACT UniProt-feature []
-property_value: DiffAvg "59.09" xsd:float
-property_value: DiffFormula "C 3 H 7 N 0 O 1" xsd:string
-property_value: DiffMono "59.049141" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 9 H 19 N 2 O 2" xsd:string
-property_value: MassAvg "187.26" xsd:float
-property_value: MassMono "187.144104" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:445
-xref: uniprot.ptm:PTM-0186
-is_a: MOD:00602
-is_a: MOD:00912
-relationship: has_functional_parent MOD:00037
-relationship: has_functional_parent MOD:00083
-
-[Term]
-id: MOD:00365
-name: N-(L-isoglutamyl)-glycine
-def: "A protein modification that effectively crosslinks an L-glutamic acid residue and a glycine residue by an isopeptide bond to form N-(L-isoglutamyl)-glycine." [PubMed:14531691, RESID:AA0360]
-comment: Cross-link 2.
-synonym: "(S)-2-amino-5-(carboxymethyl)amino-5-oxopentanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-N5-(carboxymethyl)-pentanediamic acid" EXACT RESID-alternate []
-synonym: "CROSSLNK Isoglutamyl glycine isopeptide (Gly-Glu)" EXACT UniProt-feature []
-synonym: "isoglutamyl glycine" EXACT RESID-alternate []
-synonym: "N-(L-isoglutamyl)-glycine" EXACT RESID-name []
-synonym: "N-gamma-glutamylglycine" EXACT RESID-alternate []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 7 H 9 N 2 O 3" xsd:string
-property_value: MassAvg "169.16" xsd:float
-property_value: MassMono "169.061317" xsd:float
-property_value: Origin "E, G" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0157
-is_a: MOD:00688
-is_a: MOD:02045
-is_a: MOD:02047
-is_a: MOD:00954
-
-[Term]
-id: MOD:00366
-name: O-sulfo-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O-sulfo-L-serine." [PubMed:14752058, RESID:AA0361, Unimod:40#S]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-(sulfooxy)propanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-3-hydroxypropanoic acid 3-sulfate" EXACT RESID-alternate []
-synonym: "MOD_RES Sulfoserine" EXACT UniProt-feature []
-synonym: "O-sulfo-L-serine" EXACT RESID-name []
-synonym: "O-Sulfonation" RELATED Unimod-description []
-synonym: "O3-sulfonoserine" EXACT RESID-alternate []
-synonym: "O3-sulfoserine" EXACT RESID-alternate []
-synonym: "serine sulfate ester" EXACT RESID-alternate []
-synonym: "Sulfo" RELATED PSI-MS-label []
-property_value: DiffAvg "80.06" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 3 S 1" xsd:string
-property_value: DiffMono "79.956815" xsd:float
-property_value: Formula "C 3 H 5 N 1 O 5 S 1" xsd:string
-property_value: MassAvg "167.13" xsd:float
-property_value: MassMono "166.988843" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:40
-xref: uniprot.ptm:PTM-0284
-is_a: MOD:00695
-is_a: MOD:00771
-is_a: MOD:00916
-
-[Term]
-id: MOD:00367
-name: O-sulfo-L-threonine
-def: "A protein modification that effectively converts an L-threonine residue to O-sulfo-L-threonine." [PubMed:14752058, RESID:AA0362, Unimod:40#T]
-subset: PSI-MOD-slim
-synonym: "(2S,3R)-2-amino-3-(sulfooxy)butanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-3-hydroxybutanoic acid 3-sulfate" EXACT RESID-alternate []
-synonym: "MOD_RES Sulfothreonine" EXACT UniProt-feature []
-synonym: "O-sulfo-L-threonine" EXACT RESID-name []
-synonym: "O-Sulfonation" RELATED Unimod-description []
-synonym: "O3-sulfonothreonine" EXACT RESID-alternate []
-synonym: "O3-sulfothreonine" EXACT RESID-alternate []
-synonym: "Sulfo" RELATED PSI-MS-label []
-synonym: "threonine sulfate ester" EXACT RESID-alternate []
-property_value: DiffAvg "80.06" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 3 S 1" xsd:string
-property_value: DiffMono "79.956815" xsd:float
-property_value: Formula "C 4 H 7 N 1 O 5 S 1" xsd:string
-property_value: MassAvg "181.16" xsd:float
-property_value: MassMono "181.004493" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:40
-xref: uniprot.ptm:PTM-0285
-is_a: MOD:00695
-is_a: MOD:00773
-is_a: MOD:00917
-
-[Term]
-id: MOD:00368
-name: N-carboxy-L-methionine
-def: "A protein modification that effectively converts an L-methionine residue to N-carboxy-L-methionine." [PubMed:10368287, PubMed:11120890, PubMed:12595263, PubMed:8312270, RESID:AA0363, Unimod:299#M]
-comment: At least three protein crystallographic structures have been reported with this modification. However, no chemical evidence for this modification is provided, there were no reports of this modification before these crystallographic reports, and there is no metabolic explanation for the conversion of a formyl group to a carboxy group. There is confusion in its description, and misnaming is common. This modification is probably a misidentification of N-(dihydroxymethyl)methionine, the hydrated form of N-formylmethionine. See MOD:01446 [JSG].
-synonym: "(S)-2-carboxyamino-4-(methylsulfanyl)butanoic acid" EXACT RESID-systematic []
-synonym: "2-carbamic-4-(methylsulfanyl)butanoic acid" EXACT RESID-alternate []
-synonym: "2-carbamic-4-(methylthio)butanoic acid" EXACT RESID-alternate []
-synonym: "Carboxy" RELATED Unimod-interim []
-synonym: "Carboxylation" RELATED Unimod-description []
-synonym: "N-carboxy-L-methionine" EXACT RESID-name []
-synonym: "N-carboxymethionine" EXACT RESID-alternate []
-property_value: DiffAvg "44.01" xsd:float
-property_value: DiffFormula "C 1 H 0 N 0 O 2 S 0" xsd:string
-property_value: DiffMono "43.989829" xsd:float
-property_value: Formula "C 6 H 10 N 1 O 3 S 1" xsd:string
-property_value: MassAvg "176.21" xsd:float
-property_value: MassMono "176.038139" xsd:float
-property_value: Origin "M" xsd:string
-property_value: Source "hypothetical" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:299
-is_a: MOD:00913
-is_a: MOD:01152
-
-[Term]
-id: MOD:00369
-name: O-acetyl-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O-acetyl-L-serine." [ChEBI:17981, PubMed:11857757, PubMed:11999733, PubMed:12175151, PubMed:14730666, PubMed:15350136, PubMed:16731519, PubMed:489587, PubMed:7309355, RESID:AA0364, Unimod:1#S]
-comment: incidental to RESID:AA0051
-subset: PSI-MOD-slim
-synonym: "(2S)-3-(acetyloxy)-2-aminopropanoic acid" EXACT RESID-systematic []
-synonym: "Acetyl" RELATED PSI-MS-label []
-synonym: "Acetylation" RELATED Unimod-description []
-synonym: "MOD_RES O-acetylserine" EXACT UniProt-feature []
-synonym: "O-acetyl-L-serine" EXACT RESID-name []
-synonym: "O-acetylated L-serine" EXACT PSI-MOD-alternate []
-synonym: "O-acetylserine" EXACT RESID-alternate []
-synonym: "OAcSer" EXACT PSI-MOD-label []
-synonym: "serine acetate ester" EXACT RESID-alternate []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 2 H 2 N 0 O 1" xsd:string
-property_value: DiffMono "42.010565" xsd:float
-property_value: Formula "C 5 H 7 N 1 O 3" xsd:string
-property_value: MassAvg "129.12" xsd:float
-property_value: MassMono "129.042593" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:1
-xref: uniprot.ptm:PTM-0232
-is_a: MOD:00644
-is_a: MOD:00647
-is_a: MOD:02003
-
-[Term]
-id: MOD:00370
-name: (E)-2,3-didehydrotyrosine
-def: "A protein modification that effectively converts an L-tyrosine residue to (E)-2,3-didehydrotyrosine." [PubMed:12623015, RESID:AA0365]
-comment: incidental to RESID:AA0184; incidental to RESID:AA0187; incidental to RESID:AA0188; incidental to RESID:AA0189; incidental to RESID:AA0378; incidental to RESID:AA0379; incidental to RESID:AA0380; incidental to RESID:AA0381
-subset: PSI-MOD-slim
-synonym: "(2E)-2-amino-3-(4-hydroxyphenyl)prop-2-enoic acid" EXACT RESID-systematic []
-synonym: "(E)-2,3-didehydrogenated tyrosine" EXACT PSI-MOD-alternate []
-synonym: "(E)-2,3-didehydrotyrosine" EXACT RESID-name []
-synonym: "2-amino-3-oxo-butanoic_acid" RELATED Unimod-description []
-synonym: "amino-(para-hydroxybenzylidenyl)acetic acid" EXACT RESID-alternate []
-synonym: "blue non-fluorescent pocilloporin chromophore" EXACT RESID-alternate []
-synonym: "Didehydro" RELATED PSI-MS-label []
-synonym: "E-dHTyr" EXACT PSI-MOD-label []
-synonym: "MOD_RES (E)-2,3-didehydrotyrosine" EXACT UniProt-feature []
-synonym: "para-hydroxybenzylidene-imidazolidinone chromophore" EXACT RESID-alternate []
-synonym: "trans-dehydrotyrosine" EXACT RESID-alternate []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 9 H 7 N 1 O 2" xsd:string
-property_value: MassAvg "161.16" xsd:float
-property_value: MassMono "161.047678" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0001
-is_a: MOD:00706
-
-[Term]
-id: MOD:00371
-name: bis-L-aspartato tris-L-glutamato L-histidino calcium tetramanganese tetroxide
-def: "A protein modification that effectively converts two L-aspartic acid residues, three L-glutamic acid residues, an L-histidine residue, and a one-calcium, four-iron, four-oxygen cluster to bis-L-aspartato tris-L-glutamato L-histidino calcium tetramanganese tetroxide." [PubMed:14764885, RESID:AA0366]
-comment: Cross-link 6.
-synonym: "4Mn-Ca-4O cluster" EXACT RESID-alternate []
-synonym: "bis-L-aspartato tris-L-glutamato L-histidino calcium tetramanganese tetroxide" EXACT RESID-name []
-synonym: "mu3-1:2:3kappaO-oxido-mu3-1:3:4kappaO-oxido-mu3-2:3:4kappaO-oxido-mu4-1:2:4:5kappaO-oxido-N1'-histidino-O5-glutamato 2-manganese-O5,O5-glutamato 3-manganese-O4-aspartato 4-manganese-O4-aspartato-O5-glutamato 5-manganese" EXACT RESID-systematic []
-synonym: "photosystem II catalytic cluster" EXACT RESID-alternate []
-property_value: DiffAvg "317.78" xsd:float
-property_value: DiffFormula "C 0 Ca 1 H -6 Mn 4 N 0 O 4" xsd:string
-property_value: DiffMono "317.647480" xsd:float
-property_value: Formula "C 29 Ca 1 H 32 Mn 4 N 8 O 20" xsd:string
-property_value: MassAvg "1072.44" xsd:float
-property_value: MassMono "1071.888057" xsd:float
-property_value: Origin "D, D, E, E, E, H" xsd:string
-property_value: Source "hypothetical" xsd:string
-is_a: MOD:00740
-is_a: MOD:02066
-is_a: MOD:02068
-is_a: MOD:02070
-is_a: MOD:01482
-
-[Term]
-id: MOD:00372
-name: 3'-(3'-L-tyrosinyl)-L-tyrosine
-def: "A protein modification that effectively cross-links two L-tyrosine residues with a carbon-carbon bond to form 3'-(3'-L-tyrosinyl)-L-tyrosine." [DeltaMass:0, PubMed:14249161, PubMed:637884, PubMed:8702710, PubMed:8937563, RESID:AA0367]
-comment: Cross-link 2; From DeltaMass: Average Mass: -2.
-synonym: "(2S,2'S)-3,3'-(6,6'-dihydroxybiphenyl-3,3'-diyl)bis(2-aminopropanoic acid)" EXACT RESID-systematic []
-synonym: "3'-(L-tyros-3'-yl)-L-tyrosine" EXACT RESID-name []
-synonym: "3,3'-BiTyr (Crosslink)" EXACT DeltaMass-label []
-synonym: "6,6'-dihydroxy-(1,1'-biphenyl)-3,3'-bis(2-aminopropanoic acid)" EXACT RESID-alternate []
-synonym: "alpha,alpha'-diamino-6,6'-dihydroxy-(1,1'-biphenyl)-3,3'-dipropanoic acid" EXACT RESID-alternate []
-synonym: "bityrosine" EXACT RESID-alternate []
-synonym: "o,o-dityrosine" EXACT RESID-alternate []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 18 H 16 N 2 O 4" xsd:string
-property_value: MassAvg "324.34" xsd:float
-property_value: MassMono "324.111007" xsd:float
-property_value: Origin "Y, Y" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00692
-is_a: MOD:02058
-
-[Term]
-id: MOD:00373
-name: 3'-(O4'-L-tyrosinyl)-L-tyrosine
-def: "A protein modification that effectively cross-links L-tyrosine residues with an ether bond to form 3'-(O4'-L-tyrosinyl)-L-tyrosine." [DeltaMass:0, PubMed:12719529, PubMed:7115340, PubMed:8702710, RESID:AA0368]
-comment: Cross-link 2; secondary to RESID:AA0146; From DeltaMass: Average Mass: -2.
-synonym: "(2S)-2-amino-3-[3-(4-[(2S)-2-amino-2-carboxyethyl]phenoxy)-4-hydroxyphenyl]propanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-3-[4-(5-[(2S)-2-amino-2-carboxyethyl]-2-hydroxyphenoxy)phenyl]propanoic acid" EXACT RESID-alternate []
-synonym: "3'-(L-tyros-O4'-yl)-L-tyrosine" EXACT RESID-name []
-synonym: "CROSSLNK Isodityrosine (Tyr-Tyr)" EXACT UniProt-feature []
-synonym: "IsodiTyr (Crosslink)" EXACT DeltaMass-label []
-synonym: "isodityrosine" EXACT RESID-alternate []
-synonym: "O-(5-(2-amino-2-carboxyethyl)-2-hydroxyphenyl)-L-tyrosine" EXACT RESID-alternate []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 18 H 16 N 2 O 4" xsd:string
-property_value: MassAvg "324.34" xsd:float
-property_value: MassMono "324.111007" xsd:float
-property_value: Origin "Y, Y" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0155
-is_a: MOD:00692
-is_a: MOD:02058
-
-[Term]
-id: MOD:00374
-name: 3,4-dihydroxy-L-arginine
-def: "A protein modification that effectively converts an L-arginine residue to 3,4-dihydroxy-L-arginine." [PubMed:10978343, PubMed:12686488, RESID:AA0369, Unimod:425#R, ChEBI:141829]
-synonym: "(2S,3Xi,4Xi)-2-amino-5-carbamimidamido-3,4-dihydroxypentanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-5-guanidino-3,4-dihydroxypentanoic acid" EXACT RESID-alternate []
-synonym: "3,4-dihydroxy-L-arginine" EXACT RESID-name []
-synonym: "3,4-dihydroxylated L-arginine" EXACT PSI-MOD-alternate []
-synonym: "34Hy2Arg" EXACT PSI-MOD-label []
-synonym: "beta,gamma-dihydroxyarginine" EXACT RESID-alternate []
-synonym: "dihydroxy" RELATED Unimod-description []
-synonym: "Dioxidation" RELATED PSI-MS-label []
-synonym: "MOD_RES 3,4-dihydroxyarginine" EXACT UniProt-feature []
-property_value: DiffAvg "32.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 2" xsd:string
-property_value: DiffMono "31.989829" xsd:float
-property_value: Formula "C 6 H 12 N 4 O 3" xsd:string
-property_value: MassAvg "188.19" xsd:float
-property_value: MassMono "188.090940" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:425
-xref: uniprot.ptm:PTM-0022
-is_a: MOD:00428
-is_a: MOD:00682
-
-[Term]
-id: MOD:00375
-name: 4,5-dihydroxy-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to 4,5-dihydroxy-L-lysine." [PubMed:10978343, PubMed:12686488, RESID:AA0370, Unimod:425#K]
-synonym: "(2S,4Xi,5Xi)-2,6-diamino-4,5-dihydroxyhexanoic acid" EXACT RESID-systematic []
-synonym: "4,5-dihydroxy-L-lysine" EXACT RESID-name []
-synonym: "4,5-dihydroxylated L-lysine" EXACT PSI-MOD-alternate []
-synonym: "45Hy2Lys" EXACT PSI-MOD-label []
-synonym: "alpha,epsilon-diamino-delta,gamma-dihydroxycaproic acid" EXACT RESID-alternate []
-synonym: "delta,gamma-dihydroxylysine" EXACT RESID-alternate []
-synonym: "dihydroxy" RELATED Unimod-description []
-synonym: "Dioxidation" RELATED PSI-MS-label []
-synonym: "MOD_RES 4,5-dihydroxylysine" EXACT UniProt-feature []
-property_value: DiffAvg "32.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 2" xsd:string
-property_value: DiffMono "31.989829" xsd:float
-property_value: Formula "C 6 H 12 N 2 O 3" xsd:string
-property_value: MassAvg "160.17" xsd:float
-property_value: MassMono "160.084792" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:425
-xref: uniprot.ptm:PTM-0036
-is_a: MOD:00428
-is_a: MOD:00681
-
-[Term]
-id: MOD:00376
-name: 1'-(phospho-5'-adenosine)-L-histidine
-def: "A protein modification that effectively crosslinks an L-histidine residue and 5'-phosphoadenosine through a phosphoramide ester bond to form 1'-(phospho-5'-adenosine)-L-histidine." [PubMed:15182206, PubMed:9323207, RESID:AA0371, Unimod:405#H]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-[1-(5'-adenosine phosphono)imidazol-4-yl]propanoic acid" EXACT RESID-systematic []
-synonym: "1'-(phospho-5'-adenosine)-L-histidine" EXACT RESID-name []
-synonym: "ACT_SITE Tele-AMP-histidine intermediate" EXACT UniProt-feature []
-synonym: "AMP binding site" RELATED Unimod-description []
-synonym: "L-histidine 5'-adenosine phosphoramidester" EXACT RESID-alternate []
-synonym: "L-histidine monoanhydride with 5'-adenylic acid" EXACT RESID-alternate []
-synonym: "N(tau)-5'-adenylic-L-histidine" EXACT RESID-alternate []
-synonym: "N1'-adenylylated histidine" EXACT RESID-alternate []
-synonym: "Phosphoadenosine" RELATED PSI-MS-label []
-synonym: "tele-5'-adenylic-L-histidine" EXACT RESID-alternate []
-property_value: DiffAvg "329.21" xsd:float
-property_value: DiffFormula "C 10 H 12 N 5 O 6 P 1" xsd:string
-property_value: DiffMono "329.052520" xsd:float
-property_value: Formula "C 16 H 19 N 8 O 7 P 1" xsd:string
-property_value: MassAvg "466.35" xsd:float
-property_value: MassMono "466.111432" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:405
-is_a: MOD:00909
-is_a: MOD:01165
-
-[Term]
-id: MOD:00377
-name: 1'-(phospho-5'-uridine)-L-histidine
-def: "A protein modification that effectively crosslinks an L-histidine residue and 5'-phosphouridine through a phosphoramide ester bond to form 1'-(phospho-5'-uridine)-L-histidine." [PubMed:11467524, PubMed:321007, PubMed:380639, PubMed:8794735, RESID:AA0372, Unimod:417#H]
-subset: PSI-MOD-slim
-synonym: "(S)-2-amino-3-[1-(5'-uridine phosphono)imidazol-4-yl]propanoic acid" EXACT RESID-systematic []
-synonym: "1'-(phospho-5'-uridine)-L-histidine" EXACT RESID-name []
-synonym: "ACT_SITE Tele-UMP-histidine intermediate" EXACT UniProt-feature []
-synonym: "L-histidine 5'-uridine phosphoramidester" EXACT RESID-alternate []
-synonym: "L-histidine monoanhydride with 5'-uridylic acid" EXACT RESID-alternate []
-synonym: "N(tau)-5'-uridylic-L-histidine" EXACT RESID-alternate []
-synonym: "N1'-uridylylated histidine" EXACT RESID-alternate []
-synonym: "PhosphoUridine" RELATED PSI-MS-label []
-synonym: "tele-5'-uridylic-L-histidine" EXACT RESID-alternate []
-synonym: "uridine phosphodiester" RELATED Unimod-description []
-synonym: "MOD_RES O-UMP-histidine" EXACT UniProt-feature []
-property_value: DiffAvg "306.17" xsd:float
-property_value: DiffFormula "C 9 H 11 N 2 O 8 P 1" xsd:string
-property_value: DiffMono "306.025302" xsd:float
-property_value: Formula "C 15 H 18 N 5 O 9 P 1" xsd:string
-property_value: MassAvg "443.31" xsd:float
-property_value: MassMono "443.084214" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:417
-xref: uniprot.ptm:PTM-0500
-is_a: MOD:00909
-is_a: MOD:01166
-
-[Term]
-id: MOD:00378
-name: L-aspartyl semialdehyde
-def: "A protein modification that effectively converts an L-aspartic acid residue to L-aspartyl semialdehyde." [PubMed:1093385, PubMed:14235557, PubMed:15237995, RESID:AA0373, Unimod:447#D]
-subset: PSI-MOD-slim
-synonym: "(S)-2-amino-4-oxobutanoic acid" EXACT RESID-systematic []
-synonym: "aspartyl 4-semialdehyde" EXACT PSI-MOD-alternate []
-synonym: "aspartyl aldehyde" EXACT PSI-MOD-alternate []
-synonym: "Deoxy" RELATED PSI-MS-label []
-synonym: "L-aminosuccinaldehydic acid" EXACT RESID-alternate []
-synonym: "L-aminosuccinic acid semialdehyde" EXACT RESID-alternate []
-synonym: "L-aspartate-beta-semialdehyde" EXACT RESID-alternate []
-synonym: "L-aspartic beta-semialdehyde" EXACT RESID-alternate []
-synonym: "L-aspartyl aldehyde" EXACT RESID-name []
-synonym: "L-beta-formylalanine" EXACT RESID-alternate []
-synonym: "MOD_RES Aspartyl aldehyde" EXACT UniProt-feature []
-synonym: "reduction" RELATED Unimod-description []
-property_value: DiffAvg "-16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O -1" xsd:string
-property_value: DiffMono "-15.994915" xsd:float
-property_value: Formula "C 4 H 5 N 1 O 2" xsd:string
-property_value: MassAvg "99.09" xsd:float
-property_value: MassMono "99.032028" xsd:float
-property_value: Origin "D" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:447
-xref: uniprot.ptm:PTM-0064
-is_a: MOD:00904
-is_a: MOD:01161
-
-[Term]
-id: MOD:00379
-name: L-serine microcin E492 siderophore ester
-def: "A protein modification that effectively converts an L-serine residue to L-serine microcin E492 siderophore ester." [PubMed:15102848, RESID:AA0374, Unimod:448#C-term]
-comment: Unimod origin corrected [JSG].
-synonym: "L-serine microcin E492 siderophore ester" EXACT RESID-name []
-synonym: "Microcin" RELATED PSI-MS-label []
-synonym: "microcin E492 siderophore ester from serine" RELATED Unimod-description []
-synonym: "MOD_RES Serine microcin E492 siderophore ester" EXACT UniProt-feature []
-synonym: "N-[5-(6-O-seryl-beta-glucosyl)-2,3-dihydroxybenzoyl]-O-[N-(2,3-dihydroxybenzoyl)-O-[N-(2,3-dihydroxybenzoyl)seryl]seryl]serine" EXACT RESID-systematic []
-property_value: DiffAvg "831.69" xsd:float
-property_value: DiffFormula "C 36 H 37 N 3 O 20" xsd:string
-property_value: DiffMono "831.197041" xsd:float
-property_value: Formula "C 39 H 43 N 4 O 23" xsd:string
-property_value: MassAvg "935.78" xsd:float
-property_value: MassMono "935.231809" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: Unimod:448
-xref: uniprot.ptm:PTM-0276
-is_a: MOD:00916
-
-[Term]
-id: MOD:00380
-name: L-aspartyl molybdenum bis(molybdopterin guanine dinucleotide)
-def: "A protein modification that effectively converts an L-aspartic acid residue to L-aspartyl molybdenum bis(molybdopterin guanine dinucleotide)." [PubMed:12910261, PubMed:14725769, RESID:AA0375, Unimod:424#D]
-synonym: "2-amino-5,6-dimercapto-7-methyl-3,7,8a,9-tetrahydro-8-oxa-1,3,9,10-tetraazaanthracen-4-one guanosine dinucleotide" EXACT RESID-alternate []
-synonym: "bis[8-amino-1a,2,4a,5,6,7,10-heptahydro-2-(trihydrogen diphosphate 5'-ester with guanosine)methyl-6-oxo-3,4-disulfanyl-pteridino[6,7-5,6]pyranoato-S3,S4]-aspartyl-molybdenum" EXACT RESID-systematic []
-synonym: "L-aspartyl molybdenum bis(molybdopterin guanine dinucleotide)" EXACT RESID-name []
-synonym: "molybdenum bis(molybdopterin guanine dinucleotide)" RELATED Unimod-description []
-synonym: "MolybdopterinGD" RELATED PSI-MS-label []
-synonym: "nitrate reductase A aspartyl Mo-bisMGD cofactor" EXACT RESID-alternate []
-synonym: "phosphoric acid 4-(2-amino-4-oxo-3,4,5,6,-tetrahydro-pteridin-6-yl)-2-hydroxy-3,4-dimercapto-but-3-en-yl ester guanylate ester" EXACT RESID-alternate []
-property_value: DiffAvg "1572.02" xsd:float
-property_value: DiffFormula "C 40 H 47 Mo 1 N 20 O 26 P 4 S 4" xsd:string
-property_value: DiffMono "1572.985775" xsd:float
-property_value: Formula "C 44 H 52 Mo 1 N 21 O 29 P 4 S 4" xsd:string
-property_value: MassAvg "1687.10" xsd:float
-property_value: MassMono "1688.012718" xsd:float
-property_value: Origin "D" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:424
-is_a: MOD:02066
-is_a: MOD:01167
-
-[Term]
-id: MOD:00381
-name: L-selenocysteinyl tungsten bis(molybdopterin guanine dinucleotide) (Sec)
-def: "A protein modification that effectively converts an L-selenocysteine residue to L-selenocysteinyl tungsten bis(molybdopterin guanine dinucleotide)." [PubMed:11372198, PubMed:12220497, RESID:AA0376#SEC]
-property_value: DiffAvg "1691.97" xsd:float
-property_value: DiffFormula "C 40 H 47 N 20 O 26 P 4 S 5 Se 0 W 1" xsd:string
-property_value: DiffMono "1691.003369" xsd:float
-property_value: Formula "C 43 H 52 N 21 O 27 P 4 S 5 Se 1 W 1" xsd:string
-property_value: MassAvg "1842.02" xsd:float
-property_value: MassMono "1841.957004" xsd:float
-property_value: Origin "U" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00746
-is_a: MOD:00748
-is_a: MOD:02073
-
-[Term]
-id: MOD:00382
-name: 3-(2-methylthio)ethyl-6-(4-hydroxybenzylidene)-5-iminopiperazin-2-one
-def: "A protein modification that effectively crosslinks an L-methionyl-L-tyrosine dipeptide to form 3-(2-methylthio)ethyl-6-(4-hydroxybenzylidene)-5-iminopiperazin-2-one." [PubMed:10852900, PubMed:11259412, PubMed:15491166, RESID:AA0377]
-comment: carboxamidine; cross-link 1. This is a deprecated entry in RESID. It probably does not occur naturally [JSG].
-synonym: "3-(2-methylsulfanyl)ethyl-6-(4-hydroxybenzylidene)-5-iminopiperazin-2-one" EXACT RESID-systematic []
-synonym: "3-(2-methylthio)ethyl-6-(4-hydroxybenzylidene)-5-amino-3,6-didehydropyrazin-2-ol" EXACT RESID-alternate []
-synonym: "3-(2-methylthio)ethyl-6-(4-hydroxybenzylidene)-5-iminopiperazin-2-one" EXACT RESID-name []
-synonym: "GFP-like chromoprotein asFP595 chromophore" EXACT RESID-alternate []
-synonym: "L-methionyl-L-tyrosyl-2-keto-5-iminopiperazine" EXACT RESID-alternate []
-property_value: DiffAvg "-20.03" xsd:float
-property_value: DiffFormula "C 0 H -4 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-20.026215" xsd:float
-property_value: Formula "C 14 H 15 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "275.35" xsd:float
-property_value: MassMono "275.085424" xsd:float
-property_value: Origin "M, Y" xsd:string
-property_value: Source "hypothetical" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:02052
-is_a: MOD:02058
-
-[Term]
-id: MOD:00383
-name: 2-imino-glutamic acid 5-imidazolinone glycine
-def: "A protein modification that effectively crosslinks an L-glutamic acid residue and a glycine residue to form 2-imino-glutamic acid 5-imidazolinone glycine." [PubMed:11682051, RESID:AA0378]
-comment: Cross-link 2; carboxamidine; cross-link 1; incidental to RESID:AA0183; incidental to RESID:AA0365.
-synonym: "2,N-didehydroglutamyl-5-imidazolinone glycine" EXACT RESID-alternate []
-synonym: "2-(3-carboxy-1-iminopropyl)-1-carboxymethyl-1-imidazolin-5-one" EXACT RESID-alternate []
-synonym: "2-imino-glutamic acid 5-imidazolinone glycine" EXACT RESID-name []
-synonym: "2-imino-glutamyl-5-imidazolinone glycine" EXACT RESID-alternate []
-synonym: "4-[1-(carboxymethyl)-5-oxo-4,5-dihydro-1H-imidazol-2-yl]-4-iminobutanoic acid" EXACT RESID-systematic []
-synonym: "[2-(3-carboxy-1-iminopropyl)-5-oxo-4,5-dihydro-imidazol-1-yl]-acetic acid" EXACT RESID-alternate []
-synonym: "CROSSLNK 2-iminomethyl-5-imidazolinone (Glu-Gly)" EXACT UniProt-feature []
-synonym: "para-hydroxybenzylidene-imidazolidinone chromophore" EXACT RESID-alternate []
-property_value: DiffAvg "-20.03" xsd:float
-property_value: DiffFormula "C 0 H -4 N 0 O -1" xsd:string
-property_value: DiffMono "-20.026215" xsd:float
-property_value: Formula "C 7 H 6 N 2 O 3" xsd:string
-property_value: MassAvg "166.14" xsd:float
-property_value: MassMono "166.037842" xsd:float
-property_value: Origin "E, G" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: uniprot.ptm:PTM-0014
-is_a: MOD:02045
-is_a: MOD:02047
-is_a: MOD:01882
-
-[Term]
-id: MOD:00384
-name: 2-imino-methionine 5-imidazolinone glycine
-def: "A protein modification that effectively crosslinks an L-methionine residue and a glycine residue to form 2-imino-methionine 5-imidazolinone glycine." [PubMed:10852900, PubMed:12185250, PubMed:12909624, PubMed:15542608, RESID:AA0379]
-comment: Cross-link 2; carboxamidine; cross-link 1; incidental to RESID:AA0183; incidental to RESID:AA0365.
-synonym: "(2-[1-imino-3-(methylsulfanyl)propyl]-5-oxo-4,5-dihydro-imidazol-1-yl)acetic acid" EXACT RESID-alternate []
-synonym: "(2-[3-(methylsulfanyl)propanimidoyl]-5-oxo-4,5-dihydro-1H-imidazol-1-yl)acetic acid" EXACT RESID-systematic []
-synonym: "2,N-didehydromethionyl-5-imidazolinone glycine" EXACT RESID-alternate []
-synonym: "2-[1-imino-3-(methylsulfanyl)propyl]-1-carboxymethyl-1-imidazolin-5-one" EXACT RESID-alternate []
-synonym: "2-imino-methionine 5-imidazolinone glycine" EXACT RESID-name []
-synonym: "2-imino-methionyl-5-imidazolinone glycine" EXACT RESID-alternate []
-synonym: "CROSSLNK 2-iminomethyl-5-imidazolinone (Met-Gly)" EXACT UniProt-feature []
-synonym: "GFP-like chromoprotein asFP595 chromophore" EXACT RESID-alternate []
-synonym: "para-hydroxybenzylidene-imidazolidinone chromophore" EXACT RESID-alternate []
-synonym: "red fluorescent protein eqFP611 chromophore" EXACT RESID-alternate []
-property_value: DiffAvg "-20.03" xsd:float
-property_value: DiffFormula "C 0 H -4 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-20.026215" xsd:float
-property_value: Formula "C 7 H 8 N 2 O 1 S 1" xsd:string
-property_value: MassAvg "168.21" xsd:float
-property_value: MassMono "168.035734" xsd:float
-property_value: Origin "G, M" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0015
-is_a: MOD:02047
-is_a: MOD:02052
-is_a: MOD:01882
-
-[Term]
-id: MOD:00385
-name: L-asparagine 5-imidazolinone glycine
-def: "A protein modification that effectively crosslinks an L-asparagine residue and a glycine residue to form L-asparagine 5-imidazolinone glycine." [PubMed:10504696, RESID:AA0380]
-comment: Cross-link 2; carboxamidine; incidental to RESID:AA0183; incidental to RESID:AA0365.
-synonym: "(2-[(1S)-1,3-diamino-3-oxopropyl]-5-oxo-4,5-dihydro-1H-imidazol-1-yl)acetic acid" EXACT RESID-systematic []
-synonym: "2-[(S)-1,3-diamino-3-oxopropyl]-1-carboxymethyl-1-imidazolin-5-one" EXACT RESID-alternate []
-synonym: "[2-(1,3-diamino-3-oxopropyl)-5-oxo-4,5-dihydro-imidazol-1-yl]-acetic acid" EXACT RESID-alternate []
-synonym: "asparaginyl-5-imidazolinone glycine" EXACT RESID-alternate []
-synonym: "CROSSLNK 5-imidazolinone (Asn-Gly)" EXACT UniProt-feature []
-synonym: "L-asparagine 5-imidazolinone glycine" EXACT RESID-name []
-synonym: "para-hydroxybenzylidene-imidazolidinone chromophore" EXACT RESID-alternate []
-synonym: "Zoanthus sp. fluorescent protein FP506 chromophore" EXACT RESID-alternate []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 6 H 7 N 3 O 2" xsd:string
-property_value: MassAvg "153.14" xsd:float
-property_value: MassMono "153.053826" xsd:float
-property_value: Origin "G, N" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: uniprot.ptm:PTM-0046
-is_a: MOD:02042
-is_a: MOD:02047
-is_a: MOD:01882
-is_a: MOD:00954
-
-[Term]
-id: MOD:00386
-name: L-lysine 5-imidazolinone glycine
-def: "A protein modification that effectively crosslinks an L-lysine residue and a glycine residue to form L-lysine 5-imidazolinone glycine." [PubMed:10504696, RESID:AA0381]
-comment: Cross-link 2; carboxamidine; incidental to RESID:AA0183; incidental to RESID:AA0365.
-synonym: "(2-[(1S)-1,5-diaminopentyl]-5-oxo-4,5-dihydro-1H-imidazol-1-yl)acetic acid" EXACT RESID-systematic []
-synonym: "2-[(S)-1,5-diaminopentanyl]-1-carboxymethyl-1-imidazolin-5-one" EXACT RESID-alternate []
-synonym: "[2-(1,5-diaminopentanyl)-5-oxo-4,5-dihydro-imidazol-1-yl]-acetic acid" EXACT RESID-alternate []
-synonym: "Anemonia majano fluorescent protein FP486 chromophore" EXACT RESID-alternate []
-synonym: "CROSSLNK 5-imidazolinone (Lys-Gly)" EXACT UniProt-feature []
-synonym: "L-lysine 5-imidazolinone glycine" EXACT RESID-name []
-synonym: "lysyl-5-imidazolinone glycine" EXACT RESID-alternate []
-synonym: "para-hydroxybenzylidene-imidazolidinone chromophore" EXACT RESID-alternate []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 8 H 13 N 3 O 1" xsd:string
-property_value: MassAvg "167.21" xsd:float
-property_value: MassMono "167.105862" xsd:float
-property_value: Origin "G, K" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: uniprot.ptm:PTM-0048
-is_a: MOD:02047
-is_a: MOD:02051
-is_a: MOD:01882
-is_a: MOD:00954
-
-[Term]
-id: MOD:00387
-name: 2-tetrahydropyridinyl-5-imidazolinone glycine
-def: "A protein modification that effectively crosslinks an L-lysine residue and a glycine residue to form 2-tetrahydropyridinyl-5-imidazolinone glycine." [PubMed:10504696, PubMed:15628861, RESID:AA0382]
-comment: Cross-link 2; carboxamidine; incidental to RESID:AA0183; incidental to RESID:AA0365.
-synonym: "2-(3,4,5,6-tetrahydropyridin-2-yl)-1-carboxymethyl-1-imidazolin-5-one" EXACT RESID-alternate []
-synonym: "2-(tetrahydropyrid-2-yl)-5-imidazolinone glycine" EXACT RESID-alternate []
-synonym: "2-tetrahydropyridinyl-5-imidazolinone glycine" EXACT RESID-name []
-synonym: "[5-oxo-2-(3,4,5,6-tetrahydropyridin-2-yl)-4,5-dihydro-1H-imidazol-1-yl]acetic acid" EXACT RESID-alternate []
-synonym: "[5-oxo-2-(3,4,5,6-tetrahydropyridin-2-yl)-4,5-dihydro-1H-imidazol-1-yl]acetic acid" EXACT RESID-systematic []
-synonym: "CROSSLNK 2-tetrahydro-2-pyridyl-5-imidazolinone (Lys-Gly)" EXACT UniProt-feature []
-synonym: "para-hydroxybenzylidene-imidazolidinone chromophore" EXACT RESID-alternate []
-synonym: "Zoanthus sp. fluorescent protein zFP538 chromophore" EXACT RESID-alternate []
-property_value: DiffAvg "-37.06" xsd:float
-property_value: DiffFormula "C 0 H -7 N -1 O -1" xsd:string
-property_value: DiffMono "-37.052764" xsd:float
-property_value: Formula "C 8 H 9 N 2 O 1" xsd:string
-property_value: MassAvg "149.17" xsd:float
-property_value: MassMono "149.071488" xsd:float
-property_value: Origin "G, K" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0018
-is_a: MOD:02047
-is_a: MOD:02051
-is_a: MOD:01882
-
-[Term]
-id: MOD:00388
-name: L-alanyl-pentaglycyl-murein peptidoglycan
-def: "A protein modification that effectively attaches an L-alanine residue to murein peptidoglycan by a pentaglycine linker peptide." [PubMed:8163519, RESID:AA0383]
-synonym: "(2R,6S)-2-(N-mureinyl-(R)-alanyl-(S)-isoglutamyl)amino-6-(alanyl-pentaglycyl)amino-pimeloyl-(S)-alanyl-(S)-alanine" EXACT RESID-alternate []
-synonym: "L-alanyl-pentaglycyl-murein peptidoglycan" EXACT RESID-name []
-synonym: "MOD_RES Pentaglycyl murein peptidoglycan amidated alanine" EXACT UniProt-feature []
-property_value: Origin "A" xsd:string
-property_value: Source "hypothetical" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0245
-is_a: MOD:00901
-is_a: MOD:01159
-
-[Term]
-id: MOD:00389
-name: N-formyl-L-proline
-def: "A protein modification that effectively converts an L-proline residue to N-formyl-L-proline." [PubMed:12051774, PubMed:5464655, RESID:AA0384, Unimod:122#N-term]
-comment: CAUTION - observations of this modification can be attributed to unintended artifactual production, or to spurious peptide MS identification. This modification is probably not a natural post-translational modification [JSG].
-synonym: "(2S)-1-formylpyrrolidine-2-carboxylic acid" EXACT RESID-systematic []
-synonym: "1-formyl-2-pyrrolidinecarboxylic acid" EXACT RESID-alternate []
-synonym: "1-formylproline" EXACT RESID-alternate []
-synonym: "N-formyl-L-proline" EXACT RESID-name []
-synonym: "N-formylated L-proline" EXACT PSI-MOD-alternate []
-synonym: "NFoPro" EXACT PSI-MOD-label []
-property_value: DiffAvg "28.01" xsd:float
-property_value: DiffFormula "C 1 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "27.994915" xsd:float
-property_value: Formula "C 6 H 8 N 1 O 2" xsd:string
-property_value: MassAvg "126.14" xsd:float
-property_value: MassMono "126.055504" xsd:float
-property_value: Origin "P" xsd:string
-property_value: Source "hypothetical" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:122
-is_a: MOD:00409
-is_a: MOD:00915
-is_a: MOD:01696
-
-[Term]
-id: MOD:00390
-name: O-decanoyl-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O-decanoyl-L-serine." [PubMed:12630926, RESID:AA0385, Unimod:449#S]
-synonym: "(2S)-2-amino-3-(decanoyloxy)propanoic acid" EXACT RESID-systematic []
-synonym: "Decanoyl" RELATED PSI-MS-label []
-synonym: "L-serine decanoate ester" EXACT RESID-alternate []
-synonym: "lipid" RELATED Unimod-description []
-synonym: "LIPID O-decanoyl serine" EXACT UniProt-feature []
-synonym: "O-decanoyl-L-serine" EXACT RESID-name []
-synonym: "O-decanoylated L-serine" EXACT PSI-MOD-alternate []
-synonym: "O3-decanoyl-L-serine" EXACT RESID-alternate []
-synonym: "ODecSer" EXACT PSI-MOD-label []
-property_value: DiffAvg "154.25" xsd:float
-property_value: DiffFormula "C 10 H 18 N 0 O 1" xsd:string
-property_value: DiffMono "154.135765" xsd:float
-property_value: Formula "C 13 H 23 N 1 O 3" xsd:string
-property_value: MassAvg "241.33" xsd:float
-property_value: MassMono "241.167794" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:449
-xref: uniprot.ptm:PTM-0234
-is_a: MOD:00668
-is_a: MOD:02003
-
-[Term]
-id: MOD:00391
-name: O-octanoyl-L-threonine
-def: "A protein modification that effectively converts an L-threonine residue to O-octanoyl-L-threonine." [PubMed:11546772, PubMed:12716131, RESID:AA0386, Unimod:426#T]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-(octanoyloxy)butanoic acid" EXACT RESID-systematic []
-synonym: "L-threonine octanoate ester" EXACT RESID-alternate []
-synonym: "LIPID O-octanoyl threonine" EXACT UniProt-feature []
-synonym: "O-octanoyl-L-threonine" EXACT RESID-name []
-synonym: "O-octanoylated L-threonine" EXACT PSI-MOD-alternate []
-synonym: "O3-octanoyl-L-threonine" EXACT RESID-alternate []
-synonym: "Octanoyl" RELATED PSI-MS-label []
-synonym: "octanoyl" RELATED Unimod-description []
-synonym: "OOctThr" EXACT PSI-MOD-label []
-property_value: DiffAvg "126.20" xsd:float
-property_value: DiffFormula "C 8 H 14 N 0 O 1" xsd:string
-property_value: DiffMono "126.104465" xsd:float
-property_value: Formula "C 12 H 21 N 1 O 3" xsd:string
-property_value: MassAvg "227.30" xsd:float
-property_value: MassMono "227.152144" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:426
-xref: uniprot.ptm:PTM-0240
-is_a: MOD:00669
-is_a: MOD:02004
-
-[Term]
-id: MOD:00392
-name: O-decanoyl-L-threonine
-def: "A protein modification that effectively converts an L-threonine residue to O-decanoyl-L-threonine." [PubMed:11546772, RESID:AA0387, Unimod:449#T]
-synonym: "(2S)-2-amino-3-(decanoyloxy)propanoic acid" EXACT RESID-systematic []
-synonym: "Decanoyl" RELATED PSI-MS-label []
-synonym: "L-threonine decanoate ester" EXACT RESID-alternate []
-synonym: "lipid" RELATED Unimod-description []
-synonym: "LIPID O-decanoyl threonine" EXACT UniProt-feature []
-synonym: "O-decanoyl-L-threonine" EXACT RESID-name []
-synonym: "O-decanoylated L-threonine" EXACT PSI-MOD-alternate []
-synonym: "O3-decanoyl-L-threonine" EXACT RESID-alternate []
-synonym: "ODecThr" EXACT PSI-MOD-label []
-property_value: DiffAvg "154.25" xsd:float
-property_value: DiffFormula "C 10 H 18 N 0 O 1" xsd:string
-property_value: DiffMono "154.135765" xsd:float
-property_value: Formula "C 14 H 25 N 1 O 3" xsd:string
-property_value: MassAvg "255.36" xsd:float
-property_value: MassMono "255.183444" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:449
-xref: uniprot.ptm:PTM-0235
-is_a: MOD:00668
-is_a: MOD:02004
-
-[Term]
-id: MOD:00393
-name: O-methylated residue
-def: "A protein modification that effectively replaces a hydroxyl group hydrogen with a methyl group to produce either an ether from an alcohol or an ester from an acid." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "OMeRes" EXACT PSI-MOD-label []
-is_a: MOD:00427
-
-[Term]
-id: MOD:00394
-name: monoacetylated residue
-def: "A protein modification that effectively replaces one hydrogen atom with one acetyl group." [DeltaMass:0, PubMed:11857757, PubMed:11999733, PubMed:12175151, PubMed:14730666, PubMed:15350136, Unimod:1]
-comment: Amino hydrogens are replaced to produce amides; hydroxyl hydrogens are replaced to produce esters; and hydrosulfanyl (thiol) hydrogens are replaced to produce sulfanyl esters (thiol esters). From DeltaMass: Average Mass: 42
-subset: PSI-MOD-slim
-synonym: "Acetyl" RELATED PSI-MS-label []
-synonym: "Acetylation" RELATED Unimod-description []
-synonym: "Acetylation (N terminus, N epsilon of Lysine, O of Serine) (Ac)" EXACT DeltaMass-label []
-synonym: "Ac1Res" EXACT PSI-MOD-label []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 2 H 2 O 1" xsd:string
-property_value: DiffMono "42.010565" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:1
-is_a: MOD:02078
-
-[Term]
-id: MOD:00395
-name: thioester crosslinked residues
-def: "A protein modification that crosslinks two residues by formation of a thioester bond between a cysteine thiol and either an alpha-carbonyl, as in S-(L-methionyl-L-cysteine), or a sidechain carbonyl, as in S-(L-isoglutamyl)-L-cysteine." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:00033
-is_a: MOD:02044
-
-[Term]
-id: MOD:00396
-name: O-glycosylated residue
-def: "A protein modification that effectively replaces a residue hydrogen atom on an oxygen with a carbohydrate-like group through a glycosidic bond." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "OGlycoRes" EXACT PSI-MOD-label []
-is_a: MOD:00693
-
-[Term]
-id: MOD:00397
-name: iodoacetamide derivatized residue
-def: "A protein modification that is produced by reaction with iodoacetamide, usually replacement of a reactive hydrogen with a methylcarboxamido group." [PubMed:11327326, PubMed:11510821, PubMed:12422359, Unimod:4]
-subset: PSI-MOD-slim
-synonym: "Carbamidomethyl" RELATED PSI-MS-label []
-synonym: "Iodoacetamide derivative" RELATED Unimod-description []
-property_value: DiffAvg "57.05" xsd:float
-property_value: DiffFormula "C 2 H 3 N 1 O 1" xsd:string
-property_value: DiffMono "57.021464" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:4
-is_a: MOD:00848
-
-[Term]
-id: MOD:00398
-name: carbamoylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with a carbamoyl (carboxamido) group. Replacement of an amino hydrogen produces a ureido group." [DeltaMass:56, PubMed:10978403, PubMed:12203680, Unimod:5]
-comment: This modification can be produced by hydrogen cyanate, either used as a reagent or as released by urea degradation in solution [JSG].
-subset: PSI-MOD-slim
-synonym: "Carbamyl" RELATED Unimod-interim []
-synonym: "Carbamylation" EXACT DeltaMass-label []
-synonym: "Carbamylation" RELATED Unimod-description []
-property_value: DiffAvg "43.02" xsd:float
-property_value: DiffFormula "C 1 H 1 N 1 O 1" xsd:string
-property_value: DiffMono "43.005814" xsd:float
-property_value: Origin "X" xsd:string
-xref: Unimod:5
-is_a: MOD:01156
-
-[Term]
-id: MOD:00399
-name: iodoacetic acid derivatized residue
-def: "A protein modification that is produced by reaction with iodoacetic acid, usually replacement of a reactive hydrogen with a methylcarboxy group." [DeltaMass:64, Unimod:6]
-comment: From DeltaMass: Average Mass: 58 Abbreviation:CmC Average Mass Change:58 Notes:Cysteine reacts with iodoacetic acid to produce carboxymethyl cysteine.
-subset: PSI-MOD-slim
-synonym: "Carboxymethyl" RELATED PSI-MS-label []
-synonym: "Carboxymethyl (on Cysteine)" EXACT DeltaMass-label []
-synonym: "Iodoacetic acid derivative" RELATED Unimod-description []
-property_value: DiffAvg "58.04" xsd:float
-property_value: DiffFormula "C 2 H 2 O 2" xsd:string
-property_value: DiffMono "58.005479" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:6
-is_a: MOD:00848
-
-[Term]
-id: MOD:00400
-name: deamidated residue
-def: "A protein modification that effectively replaces a carboxamido group with a carboxyl group, with both a gain of oxygen and loss of a nitrogen and a hydrogen." [DeltaMass:32, OMSSA:4, Unimod:7]
-comment: From DeltaMass: References:Vish Katta.
-subset: PSI-MOD-slim
-synonym: "Deamidated" RELATED PSI-MS-label []
-synonym: "Deamidation" RELATED Unimod-description []
-synonym: "Deamidation of Asparagine and Glutamine to Aspartate and Glutamate" EXACT DeltaMass-label []
-synonym: "deamidationkq" EXACT OMSSA-label []
-synonym: "dNRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "0.98" xsd:float
-property_value: DiffFormula "H -1 N -1 O 1" xsd:string
-property_value: DiffMono "0.984016" xsd:float
-property_value: Origin "X" xsd:string
-xref: Unimod:7
-is_a: MOD:01156
-
-[Term]
-id: MOD:00401
-name: Gygi ICAT(TM) d0 modified cysteine
-def: "A protein modification that is produced by formation of an adduct of a cysteine residue with the Gygi isotope-coded affinity tag d0 reagent." [PubMed:10504701, Unimod:8#C]
-synonym: "Gygi ICAT(TM) d0" RELATED Unimod-description []
-synonym: "ICAT-G" RELATED PSI-MS-label []
-property_value: DiffAvg "486.63" xsd:float
-property_value: DiffFormula "C 22 H 38 N 4 O 6 S 1" xsd:string
-property_value: DiffMono "486.251206" xsd:float
-property_value: Formula "C 25 H 43 N 5 O 7 S 2" xsd:string
-property_value: MassAvg "589.77" xsd:float
-property_value: MassMono "589.260391" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:8
-is_a: MOD:01426
-is_a: MOD:01820
-
-[Term]
-id: MOD:00402
-name: Gygi ICAT(TM) d8 modified cysteine
-def: "A protein modification that is produced by formation of an adduct of a cysteine residue with the Gygi isotope-coded affinity tag d8 reagent." [PubMed:10504701, Unimod:9#C]
-synonym: "Gygi ICAT(TM) d8" RELATED Unimod-description []
-synonym: "ICAT-G:2H(8)" RELATED PSI-MS-label []
-property_value: DiffAvg "494.30" xsd:float
-property_value: DiffFormula "C 22 (1)H 30 (2)H 8 N 4 O 6 S 1" xsd:string
-property_value: DiffMono "494.301420" xsd:float
-property_value: Formula "C 25 (1)H 35 (2)H 8 N 5 O 7 S 2" xsd:string
-property_value: MassAvg "597.31" xsd:float
-property_value: MassMono "597.310605" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:9
-is_a: MOD:01431
-is_a: MOD:01820
-
-[Term]
-id: MOD:00403
-name: homoserine
-def: "A protein modification that effectively converts an L-methionine residue to homoserine." [DeltaMass:113, OMSSA:56, Unimod:10#M]
-comment: Usually formed from methionine by reaction with cyanogen bromide, CNBr, which cleaves the peptide at the methionine carboxyl group and the following residue amino group.
-subset: PSI-MOD-slim
-synonym: "ctermpephsem" EXACT OMSSA-label []
-synonym: "Homoserine" RELATED Unimod-description []
-synonym: "Homoserine formed from Met by CNBr treatment" EXACT DeltaMass-label []
-synonym: "Met->Hse" RELATED PSI-MS-label []
-property_value: DiffAvg "-30.09" xsd:float
-property_value: DiffFormula "C -1 H -2 O 1 S -1" xsd:string
-property_value: DiffMono "-29.992806" xsd:float
-property_value: Formula "C 4 H 7 N 1 O 2" xsd:string
-property_value: MassAvg "101.10" xsd:float
-property_value: MassMono "101.047678" xsd:float
-property_value: Origin "M" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: Unimod:10
-is_a: MOD:00913
-
-[Term]
-id: MOD:00404
-name: homoserine lactone
-def: "A protein modification that effectively converts an L-methionine residue to homoserine lactone." [DeltaMass:90, OMSSA:57, Unimod:11#M]
-comment: Usually formed from methionine by reaction with cyanogen bromide, CNBr, which cleaves the peptide at the methionine carboxyl group. Under acid conditions the homoserine dehydrates to form the cyclic lactone.
-subset: PSI-MOD-slim
-synonym: "ctermpephselactm" EXACT OMSSA-label []
-synonym: "Homoserine lactone" RELATED Unimod-description []
-synonym: "Met->Hsl" RELATED Unimod-interim []
-property_value: DiffAvg "-48.10" xsd:float
-property_value: DiffFormula "C -1 H -4 S -1" xsd:string
-property_value: DiffMono "-48.003371" xsd:float
-property_value: Formula "C 4 H 5 N 1 O 1" xsd:string
-property_value: MassAvg "83.09" xsd:float
-property_value: MassMono "83.037114" xsd:float
-property_value: Origin "M" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: Unimod:11
-is_a: MOD:00601
-is_a: MOD:00913
-
-[Term]
-id: MOD:00405
-name: Applied Biosystems original ICAT(TM) d8 modified cysteine
-def: "A protein modification that is produced by formation of an adduct of a cysteine residue with the Applied Biosystems original isotope-coded affinity tag d8 reagent." [Unimod:12#C]
-subset: PSI-MOD-slim
-synonym: "Applied Biosystems original ICAT(TM) d8" RELATED Unimod-description []
-synonym: "ICAT-D:2H(8)" RELATED PSI-MS-label []
-property_value: DiffAvg "450.28" xsd:float
-property_value: DiffFormula "C 20 (1)H 26 (2)H 8 N 4 O 5 S 1" xsd:string
-property_value: DiffMono "450.275205" xsd:float
-property_value: Formula "C 23 (1)H 31 (2)H 8 N 5 O 6 S 2" xsd:string
-property_value: MassAvg "553.28" xsd:float
-property_value: MassMono "553.284390" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:12
-is_a: MOD:01431
-is_a: MOD:01820
-
-[Term]
-id: MOD:00406
-name: Applied Biosystems original ICAT(TM) d0 modified cysteine
-def: "A protein modification that is produced by formation of an adduct of a cysteine residue with the Applied Biosystems original isotope-coded affinity tag d0 reagent." [Unimod:13#C]
-subset: PSI-MOD-slim
-synonym: "Applied Biosystems original ICAT(TM) d0" RELATED Unimod-description []
-synonym: "ICAT-D" RELATED PSI-MS-label []
-property_value: DiffAvg "442.22" xsd:float
-property_value: DiffFormula "C 20 (1)H 34 N 4 O 5 S 1" xsd:string
-property_value: DiffMono "442.224991" xsd:float
-property_value: Formula "C 23 (1)H 39 N 5 O 6 S 2" xsd:string
-property_value: MassAvg "545.23" xsd:float
-property_value: MassMono "545.234176" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:13
-is_a: MOD:01426
-is_a: MOD:01820
-
-[Term]
-id: MOD:00407
-name: residue methyl ester
-def: "A protein modification that effectively replaces a carboxyl group with a carboxy methyl ester group. OBSOLETE because Unimod:14 merged with entry 34, remap to MOD:00599." [PubMed:18688235]
-synonym: "ResOMe" EXACT PSI-MOD-label []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Origin "X" xsd:string
-replaced_by: MOD:00599
-is_obsolete: true
-
-[Term]
-id: MOD:00408
-name: mono N-acetylated residue
-def: "A protein modification that effectively replaces a residue amino or imino hydrogen with an acetyl group." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "N-Acetyl" EXACT PSI-MOD-alternate []
-synonym: "N-Acetylation" EXACT PSI-MOD-alternate []
-synonym: "NAcRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 2 H 2 O 1" xsd:string
-property_value: DiffMono "42.010565" xsd:float
-property_value: Origin "X" xsd:string
-is_a: MOD:00394
-is_a: MOD:00670
-
-[Term]
-id: MOD:00409
-name: N-formylated residue
-def: "A protein modification that effectively replaces a residue amino group with a formamido group." [OMSSA:44, OMSSA:82]
-subset: PSI-MOD-slim
-synonym: "Formyl" RELATED PSI-MS-label []
-synonym: "NFoRes" EXACT PSI-MOD-label []
-synonym: "ntermformyl" EXACT OMSSA-label []
-synonym: "ntermpepformyl" EXACT OMSSA-label []
-property_value: DiffAvg "28.01" xsd:float
-property_value: DiffFormula "C 1 O 1" xsd:string
-property_value: DiffMono "27.994915" xsd:float
-property_value: Origin "X" xsd:string
-is_a: MOD:00493
-is_a: MOD:00670
-
-[Term]
-id: MOD:00410
-name: S-(N-isopropylcarboxamidomethyl)-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-(N-isopropylcarboxamidomethyl)-L-cysteine." [OMSSA:84, PubMed:11465505, PubMed:8465942, Unimod:17#C]
-synonym: "N-isopropylcarboxamidomethyl" RELATED Unimod-description []
-synonym: "NIPCAM" RELATED PSI-MS-label []
-synonym: "nipcam" EXACT OMSSA-label []
-property_value: DiffAvg "99.13" xsd:float
-property_value: DiffFormula "C 5 H 9 N 1 O 1 S 0" xsd:string
-property_value: DiffMono "99.068414" xsd:float
-property_value: Formula "C 8 H 14 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "202.27" xsd:float
-property_value: MassMono "202.077599" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:17
-is_a: MOD:00848
-is_a: MOD:00905
-
-[Term]
-id: MOD:00411
-name: O18 label
-def: "modification from Unimod Isotopic label. OBSOLETE because Unimod:18 is now merged with entry 258 remap to MOD:00581 'single 018 label'" [PubMed:18688235]
-comment: A modification from Unimod:18
-property_value: DiffAvg "2.00" xsd:float
-property_value: DiffFormula "(16)O -1 (18)O 1" xsd:string
-property_value: DiffMono "2.004246" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-replaced_by: MOD:00581
-is_obsolete: true
-
-[Term]
-id: MOD:00412
-name: oxidation
-def: "modification from Unimod artifact. OBSOLETE because Unimod entry 19 is now merged with Unimod 35 remap to MOD:00425 'monohydroxylated residue'." [PubMed:18688235]
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Origin "X" xsd:string
-replaced_by: MOD:00425
-is_obsolete: true
-
-[Term]
-id: MOD:00413
-name: biotinyl-iodoacetamidyl-3,6-dioxaoctanediamine derivatized cysteine
-def: "A protein modification that is produced by reaction of a cysteine residue with biotinyl-iodoacetamidyl-3,6-dioxaoctanediamine." [Unimod:20#C]
-synonym: "Biotinyl-iodoacetamidyl-3,6-dioxaoctanediamine" RELATED Unimod-description []
-synonym: "PEO-Iodoacetyl-LC-Biotin" RELATED Unimod-interim []
-property_value: DiffAvg "414.52" xsd:float
-property_value: DiffFormula "C 18 H 30 N 4 O 5 S 1" xsd:string
-property_value: DiffMono "414.193691" xsd:float
-property_value: Formula "C 21 H 35 N 5 O 6 S 2" xsd:string
-property_value: MassAvg "517.66" xsd:float
-property_value: MassMono "517.202876" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:20
-is_a: MOD:00848
-is_a: MOD:00905
-
-[Term]
-id: MOD:00414
-name: monomethylated L-arginine
-def: "A protein modification that effectively replaces one hydrogen atom of an L-arginine residue with one methyl group." [DeltaMass:215, OMSSA:77, Unimod:34#R]
-comment: From DeltaMass: formula incorrect, N and O reversed
-subset: PSI-MOD-slim
-synonym: "Me1Arg" EXACT PSI-MOD-label []
-synonym: "Methyl" RELATED PSI-MS-label []
-synonym: "methylr" EXACT OMSSA-label []
-synonym: "N-methyl Arginyl" EXACT DeltaMass-label []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 7 H 14 N 4 O 1" xsd:string
-property_value: MassAvg "170.22" xsd:float
-property_value: MassMono "170.116761" xsd:float
-property_value: Origin "R" xsd:string
-xref: Unimod:34
-is_a: MOD:00599
-is_a: MOD:00658
-
-[Term]
-id: MOD:00415
-name: phosphorylation without neutral loss
-def: "modification from Unimod - OBSOLETE because Unimod entry 22 is now merged with entry 21 remap to MOD:00696 'phosphorylated residue'." [PubMed:18688235]
-property_value: DiffAvg "79.98" xsd:float
-property_value: DiffFormula "H 1 O 3 P 1" xsd:string
-property_value: DiffMono "79.966331" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-replaced_by: MOD:00696
-is_obsolete: true
-
-[Term]
-id: MOD:00416
-name: phosphorylation of an hydroxyl amino acid with prompt loss of phosphate
-def: "A change resulting in an alteration of the measured molecular mass of a peptide or protein hydroxyl amino acid phosphorylated promptly followed by secondary loss of a neutral trihydrogen phosphate molecular fragment." [Unimod:23]
-comment: O4-phosphotyrosine does not lose phosphate by this mechanism. Unimod does not provide a citation for this particular modification [JSG].
-subset: PSI-MOD-slim
-synonym: "Dehydrated" RELATED Unimod-interim []
-synonym: "Dehydration" RELATED Unimod-description []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "H -2 O -1" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:23
-is_a: MOD:00432
-is_a: MOD:00704
-
-[Term]
-id: MOD:00417
-name: S-carboxamidoethyl-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-carboxamidoethyl-L-cysteine." [DeltaMass:72, OMSSA:5, PubMed:1481983, Unimod:24#C]
-comment: From DeltaMass: References: Anal. Biochem. Vol 216 No. 1 p131 (citation not found) Notes: Residual acrylamide in SDS gels can label free cysteines to produce propionamido-Cys (also known as PAM-Cys)
-synonym: "Acrylamide adduct" RELATED Unimod-description []
-synonym: "PAM-Cys" EXACT DeltaMass-label []
-synonym: "Propionamide" RELATED PSI-MS-label []
-synonym: "Propionamide or Acrylamide adduct" EXACT DeltaMass-label []
-synonym: "propionamidec" EXACT OMSSA-label []
-synonym: "S-(3-amino-3-oxopropyl)cysteine" EXACT PSI-MOD-alternate []
-synonym: "S-carbamoylethyl-L-cysteine" EXACT PSI-MOD-alternate []
-synonym: "S-propanamide-L-cysteine" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "71.08" xsd:float
-property_value: DiffFormula "C 3 H 5 N 1 O 1 S 0" xsd:string
-property_value: DiffMono "71.037114" xsd:float
-property_value: Formula "C 6 H 10 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "174.22" xsd:float
-property_value: MassMono "174.046299" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:24
-is_a: MOD:00905
-
-[Term]
-id: MOD:00418
-name: pyridylacetylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with an (pyridin-3-yl)acetyl group." [PubMed:9276974, Unimod:25]
-comment: Produced by reaction with N-[(pyrid-3-yl)acetyl]oxy-succinimide [JSG].
-synonym: "Pyridylacetyl" RELATED PSI-MS-label []
-synonym: "pyridylacetyl" RELATED Unimod-description []
-property_value: DiffAvg "119.12" xsd:float
-property_value: DiffFormula "C 7 H 5 N 1 O 1" xsd:string
-property_value: DiffMono "119.037114" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:25
-is_a: MOD:00649
-is_a: MOD:00848
-
-[Term]
-id: MOD:00419
-name: (R)-5-oxo-1,4-tetrahydrothiazine-3-carboxylic acid
-def: "A protein modification that effectively converts an L-cysteine residue to (R)-5-oxo-1,4-tetrahydrothiazine-3-carboxylic acid." [DeltaMass:336, PubMed:12643538, Unimod:26#C]
-comment: From DeltaMass: A secondary modification affecting peptides with S-carbamoylmethyl-L-cysteine (CamC) at the N-terminus. These exist in enzymatic digests of proteins that have been S-alkylated with iodoacetamide. Cyclization of N-terminal CamC gives a residue of (R)-5-oxoperhydro-1,4-thiazine-3-carboxylic acid. Peptides in which this has occurred become more hydrophobic, and lose 17 Da from the N-terminal residue.
-synonym: "(R)-5-oxoperhydro-1,4-thiazine-3-carboxylic acid" EXACT DeltaMass-label []
-synonym: "5-oxothiomorpholine-3-carboxylic acid" EXACT PSI-MOD-alternate []
-synonym: "Otc" EXACT DeltaMass-label []
-synonym: "Pyro-carbamidomethyl" RELATED Unimod-interim []
-synonym: "S-carbamoylmethylcysteine cyclization (N-terminus)" EXACT DeltaMass-label []
-synonym: "S-carbamoylmethylcysteine cyclization (N-terminus)" RELATED Unimod-description []
-property_value: DiffAvg "40.02" xsd:float
-property_value: DiffFormula "C 2 H 0 N 0 O 1 S 0" xsd:string
-property_value: DiffMono "39.994915" xsd:float
-property_value: Formula "C 5 H 6 N 1 O 2 S 1" xsd:string
-property_value: MassAvg "144.17" xsd:float
-property_value: MassMono "144.011924" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:26
-is_a: MOD:00601
-is_a: MOD:00905
-
-[Term]
-id: MOD:00420
-name: 2-pyrrolidone-5-carboxylic acid (Glu)
-def: "A protein modification that effectively converts an L-glutamic acid residue to 2-pyrrolidone-5-carboxylic acid." [DeltaMass:16, OMSSA:109, PubMed:10214721, PubMed:1836357, PubMed:3473473, PubMed:8382902, RESID:AA0031#GLU, Unimod:27#E]
-comment: From DeltaMass: References: The conversion of glutamic acid to pyroglutamic was reported for the beta-amyloid protein. Miller et al. Arch. Biochem. Biophy. (1993) 301, 41-52 [DeltaMass]. The modification in amyloid protein is probably an artifact of treatment with strong acid under anhydrous conditions. Peptides with N-terminal glutamic acid isolated from single cells of Aplysia neurons show partial conversion to pyroglutamic acid, possibly dependent on a temperature sensitive factor [JSG].
-synonym: "(2S)-5-oxo-2-pyrrolidinecarboxylic acid" EXACT RESID-systematic []
-synonym: "2-oxopyrrolidine-5-carboxylic acid" EXACT RESID-alternate []
-synonym: "2-pyrrolidone-5-carboxylic acid" EXACT RESID-name []
-synonym: "5-oxoproline" EXACT RESID-alternate []
-synonym: "5-oxopyrrolidine-2-carboxylic acid" EXACT RESID-alternate []
-synonym: "5-pyrrolidone-2-carboxylic acid" EXACT RESID-alternate []
-synonym: "Glu->pyro-Glu" RELATED PSI-MS-label []
-synonym: "MOD_RES Pyrrolidone carboxylic acid (Glu)" EXACT UniProt-feature []
-synonym: "ntermpeppyroe" EXACT OMSSA-label []
-synonym: "PCA" EXACT RESID-alternate []
-synonym: "PyrGlu(Glu)" EXACT PSI-MOD-label []
-synonym: "Pyro-glu from E" RELATED Unimod-description []
-synonym: "pyroglutamic acid" EXACT RESID-alternate []
-synonym: "Pyroglutamic Acid formed from Glutamic Acid" EXACT DeltaMass-label []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 5 H 6 N 1 O 2" xsd:string
-property_value: MassAvg "112.11" xsd:float
-property_value: MassMono "112.039853" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:27
-xref: uniprot.ptm:PTM-0262
-is_a: MOD:00906
-is_a: MOD:01048
-
-[Term]
-id: MOD:00421
-name: C-glycosylated residue
-def: "A protein modification that effectively replaces a residue hydrogen atom on a carbon with a carbohydrate-like group through a glycosidic bond." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "CGlycoRes" EXACT PSI-MOD-label []
-is_a: MOD:00693
-
-[Term]
-id: MOD:00422
-name: alpha-amino morpholine-2-acetylated residue
-def: "A protein modification that effectively replaces a residue alpha-amino- or alpha-imino-hydrogen with a morpholine-2-acetyl group." [PubMed:10446193, Unimod:29#N-term]
-comment: The Unimod name \"N-Succinimidyl-3-morpholine acetate\" appears to have been a typographical error [JSG].
-synonym: "N-Succinimidyl-2-morpholine acetate" RELATED Unimod-description []
-synonym: "N-succinimidylmorpholine-2-acetate alpha-amino derivative" EXACT PSI-MOD-alternate []
-synonym: "SMA" RELATED PSI-MS-label []
-property_value: DiffAvg "127.14" xsd:float
-property_value: DiffFormula "C 6 H 9 N 1 O 2" xsd:string
-property_value: DiffMono "127.063329" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:29
-is_a: MOD:01696
-is_a: MOD:01813
-
-[Term]
-id: MOD:00423
-name: monosodium salt
-def: "A protein modification that effectively substitutes one sodium atom for one hydrogen atom." [DeltaMass:0, Unimod:30]
-subset: PSI-MOD-slim
-synonym: "Cation:Na" RELATED PSI-MS-label []
-synonym: "Na1Res" EXACT PSI-MOD-label []
-synonym: "Sodium" EXACT DeltaMass-label []
-synonym: "Sodium adduct" RELATED Unimod-description []
-property_value: DiffAvg "21.98" xsd:float
-property_value: DiffFormula "H -1 Na 1" xsd:string
-property_value: DiffMono "21.981944" xsd:float
-property_value: Origin "X" xsd:string
-xref: Unimod:30
-is_a: MOD:00747
-
-[Term]
-id: MOD:00424
-name: S-pyridylethyl-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-pyridylethyl-L-cysteine." [DeltaMass:253, OMSSA:112, PubMed:11760118, PubMed:626389, PubMed:8297018, PubMed:8783016, Unimod:31#C]
-comment: From DeltaMass: Formula:C10H12O2N1S1 (formula incorrect, N and O reversed) Monoisotopic Mass Change:208.067 Average Mass Change:208.286 (mass incorrect, aggregate not delta) References:PE Sciex
-synonym: "PECys" EXACT DeltaMass-label []
-synonym: "Pyridylethyl" RELATED PSI-MS-label []
-synonym: "Pyridylethyl Cystenyl" EXACT DeltaMass-label []
-synonym: "S-pyridinylethyl-L-cysteine" EXACT PSI-MOD-alternate []
-synonym: "S-pyridylethylation" RELATED Unimod-description []
-synonym: "spyridylethylc" EXACT OMSSA-label []
-synonym: "vinylpyridine derivatized cysteine residue" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "105.14" xsd:float
-property_value: DiffFormula "C 7 H 7 N 1" xsd:string
-property_value: DiffMono "105.057849" xsd:float
-property_value: Formula "C 10 H 12 N 2 O 1 S 1" xsd:string
-property_value: MassAvg "208.28" xsd:float
-property_value: MassMono "208.067034" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:31
-is_a: MOD:00848
-is_a: MOD:00905
-
-[Term]
-id: MOD:00425
-name: monohydroxylated residue
-def: "A protein modification that effectively replaces one hydrogen atom with a hydroxyl group." [Unimod:35]
-subset: PSI-MOD-slim
-synonym: "Hy1Res" EXACT PSI-MOD-label []
-synonym: "Oxidation" RELATED Unimod-interim []
-synonym: "Oxidation or Hydroxylation" RELATED Unimod-description []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Origin "X" xsd:string
-xref: Unimod:35
-is_a: MOD:00677
-
-[Term]
-id: MOD:00426
-name: S-glycosylated residue
-def: "A protein modification that effectively replaces a residue hydrogen atom on a sulfur with a carbohydrate-like group through a glycosidic bond." [PubMed:18688235]
-synonym: "SGlycoRes" EXACT PSI-MOD-label []
-is_a: MOD:00693
-
-[Term]
-id: MOD:00427
-name: methylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with a methyl group." [DeltaMass:36]
-comment: From DeltaMass: Average Mass: 14 Average Mass Change:14 References:Methylation of Asparagine (found in phycobiliproteins) Klotz and Glazer (1987) J. Biol. Chem. 262; 17350-17355
-subset: PSI-MOD-slim
-synonym: "MeRes" EXACT PSI-MOD-label []
-synonym: "Methylation (N terminus, N epsilon of Lysine, O of Serine, Threonine or C terminus, N of Asparagine)" EXACT DeltaMass-label []
-is_a: MOD:00001
-
-[Term]
-id: MOD:00428
-name: dihydroxylated residue
-def: "A protein modification that effectively replaces two hydrogen atoms with two hydroxyl groups." [PubMed:12686488, Unimod:425]
-subset: PSI-MOD-slim
-synonym: "dihydroxy" RELATED Unimod-description []
-synonym: "Dioxidation" RELATED PSI-MS-label []
-synonym: "Hy2Res" EXACT PSI-MOD-label []
-property_value: DiffAvg "32.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 2" xsd:string
-property_value: DiffMono "31.989829" xsd:float
-property_value: Origin "X" xsd:string
-xref: Unimod:425
-is_a: MOD:00677
-
-[Term]
-id: MOD:00429
-name: dimethylated residue
-def: "A protein modification that effectively replaces two hydrogen atoms with two methyl groups." [DeltaMass:0, PubMed:12964758, PubMed:14570711, Unimod:36]
-comment: For amino-terminal proline residues, dimethylation can effectively only be accomplished with a protonated imino group. This process accounts only for dimethylation and not protonation. The alternative Me2+Res process accounts for both protonation and dimethylation [JSG].
-subset: PSI-MOD-slim
-synonym: "di-Methylation" RELATED Unimod-description []
-synonym: "Dimethyl" RELATED PSI-MS-label []
-synonym: "Me2Res" EXACT PSI-MOD-label []
-synonym: "N,N dimethylation (of Arginine or Lysine)" EXACT DeltaMass-label []
-property_value: DiffAvg "28.05" xsd:float
-property_value: DiffFormula "C 2 H 4" xsd:string
-property_value: DiffMono "28.031300" xsd:float
-property_value: Origin "X" xsd:string
-xref: Unimod:36
-is_a: MOD:00427
-
-[Term]
-id: MOD:00430
-name: trimethylated residue
-def: "A protein modification that effectively replaces three hydrogen atoms with three methyl groups." [PubMed:12590383, PubMed:3145979, PubMed:4304194, PubMed:6778808, PubMed:7093227, PubMed:8453381, Unimod:37]
-comment: For amino acids residues, amine trimethylation can effectively only be accomplished with an aminium, protonated primary amino, group. This process accounts only for trimethylation and not protonation. The alternative Me3+Res process accounts for both protonation and trimethylation.
-subset: PSI-MOD-slim
-synonym: "Me3Res" EXACT PSI-MOD-label []
-synonym: "tri-Methylation" RELATED Unimod-description []
-synonym: "Trimethyl" RELATED PSI-MS-label []
-property_value: DiffAvg "42.08" xsd:float
-property_value: DiffFormula "C 3 H 6" xsd:string
-property_value: DiffMono "42.046950" xsd:float
-property_value: Origin "X" xsd:string
-xref: Unimod:37
-is_a: MOD:00427
-
-[Term]
-id: MOD:00431
-name: modified residue with a secondary neutral loss
-def: "Covalent modification of, or a change resulting in an alteration of the measured molecular mass of, a peptide or protein amino acid residue with a secondary loss of a neutral molecular fragment." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "NLModRes" EXACT PSI-MOD-label []
-is_a: MOD:01157
-
-[Term]
-id: MOD:00432
-name: modified residue with neutral loss of phosphate
-def: "Covalent modification of, or a change resulting in an alteration of the measured molecular mass of, a peptide or protein amino acid residue with a secondary loss of a neutral trihydrogen phosphate molecular fragment." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "dPhosModRes" EXACT PSI-MOD-label []
-is_a: MOD:00431
-
-[Term]
-id: MOD:00433
-name: monoglucosylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with an glucose group through a glycosidic bond." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "GlcRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "162.14" xsd:float
-property_value: DiffFormula "C 6 H 10 N 0 O 5" xsd:string
-property_value: DiffMono "162.052823" xsd:float
-property_value: Origin "X" xsd:string
-is_a: MOD:00761
-is_a: MOD:00726
-
-[Term]
-id: MOD:00434
-name: hexosylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of an amino acid residue or of a modifying group with a hexose sugar group through a glycosidic bond." [DeltaMass:203, PubMed:15279557, Unimod:41]
-comment: From DeltaMass: Average Mass: 162 Formula:C6 H10 05 Monoisotopic Mass Change:162.053 Average Mass Change:162.143 References:PE Sciex.
-subset: PSI-MOD-slim
-synonym: "Hex" EXACT PSI-MOD-label []
-synonym: "Hex" RELATED PSI-MS-label []
-synonym: "Hexose" RELATED Unimod-description []
-synonym: "Hexoses (Fru, Gal, Glc, Man)" EXACT DeltaMass-label []
-synonym: "O-Glycosyl-" EXACT DeltaMass-label []
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:41
-is_a: MOD:00693
-
-[Term]
-id: MOD:00435
-name: O-phospho-L-serine with neutral loss of phosphate
-def: "Covalent modification of a peptide or protein amino acid phosphorylated serine with a secondary loss of a neutral trihydrogen phosphate molecular fragment." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "dPhosOPhosSer" EXACT PSI-MOD-label []
-property_value: DiffAvg "-97.99" xsd:float
-property_value: DiffFormula "C 0 H -3 N 0 O -4 P -1" xsd:string
-property_value: DiffMono "-97.976895" xsd:float
-property_value: Formula "C 3 H 3 N 1 O 1" xsd:string
-property_value: MassAvg "69.06" xsd:float
-property_value: MassMono "69.021464" xsd:float
-property_value: Origin "MOD:00046" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01151
-relationship: derives_from MOD:00046
-
-[Term]
-id: MOD:00436
-name: N-acetylhexosaminylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of an amino acid residue or of a modifying group with an N-acetylhexosamine group through a glycosidic bond." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "HexNAc" RELATED PSI-MS-label []
-synonym: "HexNAc" EXACT PSI-MOD-label []
-synonym: "N-Acetylhexosamine" RELATED Unimod-description []
-property_value: DiffAvg "203.19" xsd:float
-property_value: DiffFormula "C 8 H 13 N 1 O 5" xsd:string
-property_value: DiffMono "203.079373" xsd:float
-property_value: Origin "X" xsd:string
-xref: GNO:G29068FM
-is_a: MOD:00693
-
-[Term]
-id: MOD:00437
-name: farnesylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with a farnesyl group." [DeltaMass:0, PubMed:15609361, Unimod:44]
-comment: From DeltaMass: Average Mass: 204
-subset: PSI-MOD-slim
-synonym: "Farnesyl" RELATED PSI-MS-label []
-synonym: "Farnesylation" EXACT DeltaMass-label []
-synonym: "Farnesylation" RELATED Unimod-description []
-synonym: "FarnRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "204.36" xsd:float
-property_value: DiffFormula "C 15 H 24" xsd:string
-property_value: DiffMono "204.187801" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:44
-is_a: MOD:00703
-
-[Term]
-id: MOD:00438
-name: myristoylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with a myristoyl group." [DeltaMass:0, Unimod:45]
-comment: From DeltaMass: Average Mass: 210
-subset: PSI-MOD-slim
-synonym: "C14:0 aliphatic acylated residue" EXACT PSI-MOD-alternate []
-synonym: "Myristoyl" RELATED PSI-MS-label []
-synonym: "Myristoylation" EXACT DeltaMass-label []
-synonym: "Myristoylation" RELATED Unimod-description []
-synonym: "MyrRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "210.36" xsd:float
-property_value: DiffFormula "C 14 H 26 O 1" xsd:string
-property_value: DiffMono "210.198365" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:45
-is_a: MOD:00649
-is_a: MOD:01155
-
-[Term]
-id: MOD:00439
-name: O-phospho-L-threonine with neutral loss of phosphate
-def: "Covalent modification of a peptide or protein amino acid phosphorylated threonine with a secondary loss of a neutral trihydrogen phosphate molecular fragment." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "dPhosOPhosThr" EXACT PSI-MOD-label []
-property_value: DiffAvg "-97.99" xsd:float
-property_value: DiffFormula "C 0 H -3 N 0 O -4 P -1" xsd:string
-property_value: DiffMono "-97.976895" xsd:float
-property_value: Formula "C 4 H 5 N 1 O 1" xsd:string
-property_value: MassAvg "83.09" xsd:float
-property_value: MassMono "83.037114" xsd:float
-property_value: Origin "MOD:00047" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00917
-is_a: MOD:01151
-relationship: derives_from MOD:00047
-
-[Term]
-id: MOD:00440
-name: palmitoylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with a palmitoyl group." [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 238
-subset: PSI-MOD-slim
-synonym: "Palmitoyl" RELATED PSI-MS-label []
-synonym: "Palmitoylation" EXACT DeltaMass-label []
-synonym: "Palmitoylation" RELATED Unimod-description []
-synonym: "PamRes" EXACT PSI-MOD-label []
-synonym: "Hexadecanoylated residue" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "238.41" xsd:float
-property_value: DiffFormula "C 16 H 30 O 1" xsd:string
-property_value: DiffMono "238.229666" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00649
-is_a: MOD:01155
-
-[Term]
-id: MOD:00441
-name: geranylgeranylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with a geranylgeranyl group." [DeltaMass:0, PubMed:15609361, Unimod:48]
-comment: From DeltaMass: Average Mass: 272
-subset: PSI-MOD-slim
-synonym: "Geranyl-geranyl" RELATED Unimod-description []
-synonym: "GeranylGeranyl" RELATED PSI-MS-label []
-synonym: "Geranylgeranylation" EXACT DeltaMass-label []
-synonym: "GergerRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "272.48" xsd:float
-property_value: DiffFormula "C 20 H 32" xsd:string
-property_value: DiffMono "272.250401" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:48
-is_a: MOD:00703
-
-[Term]
-id: MOD:00442
-name: protonated omega-N,omega-N'-dimethylated L-arginine with secondary neutral loss of N,N'-carbodiimide
-def: "Covalent modification of a peptide or protein L-arginine residue to protonated omega-N,omega-N'-dimethylated L-arginine with secondary loss of an N,N'-carbodiimide molecular fragment." [PubMed:15835918, PubMed:18688235]
-synonym: "dCDI-NNMe2+Arg" EXACT PSI-MOD-label []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 1 H 2 N 2 O 0" xsd:string
-property_value: DiffMono "42.021798" xsd:float
-property_value: Formula "C 7 H 14 N 2 O 1" xsd:string
-property_value: MassAvg "142.20" xsd:float
-property_value: MassMono "142.110613" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00431
-is_a: MOD:00902
-
-[Term]
-id: MOD:00443
-name: protonated omega-N,omega-N-dimethlyated L-arginine with secondary neutral loss of N,N-dimethylamine
-def: "Covalent modification of a peptide or protein L-arginine residue to protonated omega-N,omega-N-dimethlyated L-arginine with secondary neutral loss of an N,N-dimethylamine molecular fragment." [PubMed:15835918, PubMed:18688235]
-synonym: "dDMA-NoMe2+Arg" EXACT PSI-MOD-label []
-property_value: DiffAvg "59.09" xsd:float
-property_value: DiffFormula "C 2 H 7 N 2" xsd:string
-property_value: DiffMono "59.060923" xsd:float
-property_value: Formula "C 6 H 10 N 3 O 1" xsd:string
-property_value: MassAvg "140.17" xsd:float
-property_value: MassMono "140.082387" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00431
-is_a: MOD:00902
-
-[Term]
-id: MOD:00444
-name: N-palmitoyl-S-(sn-1-2,3-dipalmitoyl-glycerol)cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to N-palmitoyl-S-(sn-1-2,3-dipalmitoyl-glycerol)cysteine." [OMSSA:118, PubMed:10356335, Unimod:51]
-synonym: "N-acyl diglyceride cysteine" RELATED Unimod-description []
-synonym: "ntermpeptripalmitatec" EXACT OMSSA-label []
-synonym: "Tripalmitate" RELATED PSI-MS-label []
-property_value: DiffAvg "789.32" xsd:float
-property_value: DiffFormula "C 51 H 96 O 5" xsd:string
-property_value: DiffMono "788.725776" xsd:float
-property_value: Formula "C 54 H 101 N 1 O 6 S 1" xsd:string
-property_value: MassAvg "892.46" xsd:float
-property_value: MassMono "891.734961" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:51
-is_a: MOD:00899
-relationship: has_functional_parent MOD:01144
-
-[Term]
-id: MOD:00445
-name: L-homoarginine
-def: "A protein modification that effectively converts an L-lysine residue to L-homoarginine, such as reaction with O-methylisourea." [OMSSA:53, PubMed:11078590, PubMed:11085420, PubMed:11821862, Unimod:52]
-subset: PSI-MOD-slim
-synonym: "Guanidination" RELATED Unimod-description []
-synonym: "guanidinationk" EXACT OMSSA-label []
-synonym: "Guanidinyl" RELATED PSI-MS-label []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 1 H 2 N 2" xsd:string
-property_value: DiffMono "42.021798" xsd:float
-property_value: Formula "C 7 H 14 N 4 O 1" xsd:string
-property_value: MassAvg "170.22" xsd:float
-property_value: MassMono "170.116761" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:52
-is_a: MOD:00848
-is_a: MOD:00912
-
-[Term]
-id: MOD:00446
-name: 4-hydroxynonenal adduct
-def: "A protein modification produced by formation of an adduct of a residue with 4-hydroxynonenal." [PubMed:11327326, PubMed:15133838, Unimod:53]
-comment: 4-hydroxynonenal, a toxic lipid aldehyde, is a product of the hydroperoxide beta-cleavage degradation of omega-6 polyunsaturated fatty acids, such as arachidonic and linoleic acids [JSG].
-synonym: "4-hydroxynonenal (HNE)" RELATED Unimod-description []
-synonym: "HNE" RELATED PSI-MS-label []
-property_value: DiffAvg "156.22" xsd:float
-property_value: DiffFormula "C 9 H 16 O 2" xsd:string
-property_value: DiffMono "156.115030" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:53
-is_a: MOD:01155
-
-[Term]
-id: MOD:00447
-name: N-glucuronylated residue
-def: "A protein modification that effectively results from forming an adduct with a glucuronic acid either through a carboxyl group amide or ester bond, or through C1-glycosylation." [DeltaMass:0, PubMed:7398618, Unimod:54#N-term]
-subset: PSI-MOD-slim
-synonym: "Glucuronyl" RELATED PSI-MS-label []
-synonym: "N-Glucuronyl (N terminus)" EXACT DeltaMass-label []
-synonym: "N-glucuronylation" RELATED Unimod-description []
-property_value: DiffAvg "176.12" xsd:float
-property_value: DiffFormula "C 6 H 8 O 6" xsd:string
-property_value: DiffMono "176.032088" xsd:float
-property_value: Origin "X" xsd:string
-xref: Unimod:54
-is_a: MOD:00764
-
-[Term]
-id: MOD:00448
-name: mono-N-acetylaminoglucosylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with an N-acetylaminoglucose group through a glycosidic bond." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "GlcNAcRes" EXACT PSI-MOD-label []
-synonym: "HexNAc" RELATED PSI-MS-label []
-property_value: DiffAvg "203.19" xsd:float
-property_value: DiffFormula "C 8 H 13 N 1 O 5" xsd:string
-property_value: DiffMono "203.079373" xsd:float
-property_value: Origin "X" xsd:string
-is_a: MOD:00733
-is_a: MOD:01673
-
-[Term]
-id: MOD:00449
-name: acetate labeling reagent (N-term) (heavy form, +3amu)
-def: "modification from Unimod Isotopic label" [PubMed:11857757, PubMed:11999733, PubMed:12175151, Unimod:56]
-synonym: "Acetate labeling reagent (N-term & K) (heavy form, +3amu)" RELATED Unimod-description []
-synonym: "Acetyl:2H(3)" RELATED PSI-MS-label []
-property_value: DiffAvg "45.03" xsd:float
-property_value: DiffFormula "C 2 (1)H -1 (2)H 3 O 1" xsd:string
-property_value: DiffMono "45.029395" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:56
-is_a: MOD:01431
-
-[Term]
-id: MOD:00450
-name: acetate labeling reagent light form (K)
-def: "OBSOLETE because this isotopic label from Unimod entry 57 is deprecated" [PubMed:11857757]
-property_value: DiffAvg "42.01" xsd:float
-property_value: DiffFormula "C 2 (1)H 2 O 1" xsd:string
-property_value: DiffMono "42.010565" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-is_obsolete: true
-
-[Term]
-id: MOD:00451
-name: alpha-amino propanoylated residue
-def: "A protein modification that effectively replaces a residue alpha-amino- or alpha-imino-hydrogen with a propanoyl group." [PubMed:11857757, PubMed:11999733, PubMed:12175151, Unimod:58#N-term]
-synonym: "Propionate labeling reagent light form (N-term & K)" RELATED Unimod-description []
-synonym: "Propionyl" RELATED PSI-MS-label []
-property_value: DiffAvg "56.06" xsd:float
-property_value: DiffFormula "C 3 H 4 O 1" xsd:string
-property_value: DiffMono "56.026215" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:58
-is_a: MOD:01894
-
-[Term]
-id: MOD:00452
-name: alpha-amino 3x(13)C-labeled propanoylated residue
-def: "A protein modification that effectively replaces a residue alpha-amino- or alpha-imino-hydrogen with a 3x(13)C-labeled propanoyl group." [PubMed:11857757, PubMed:11999733, PubMed:12175151, Unimod:59#N-term]
-synonym: "Propionate labeling reagent heavy form (+3amu), N-term & K" RELATED Unimod-description []
-synonym: "Propionyl:13C(3)" RELATED PSI-MS-label []
-property_value: DiffAvg "59.04" xsd:float
-property_value: DiffFormula "(13)C 3 H 4 O 1" xsd:string
-property_value: DiffMono "59.036279" xsd:float
-property_value: Formula "(12)C 6 (13)C 3 H 16 N 2 O 2" xsd:string
-property_value: MassAvg "187.13" xsd:float
-property_value: MassMono "187.131242" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:59
-relationship: derives_from MOD:00451
-is_a: MOD:01428
-is_a: MOD:01426
-
-[Term]
-id: MOD:00453
-name: quaternary amine labeling reagent light form (N-term & K)
-def: "A protein modification that effectively replaces a residue alpha-amino- or alpha-imino-hydrogen with a quaternary amine reagent light form group." [PubMed:11857757, Unimod:60]
-synonym: "GIST-Quat" RELATED PSI-MS-label []
-synonym: "Quaternary amine labeling reagent light form (N-term & K)" RELATED Unimod-description []
-property_value: DiffAvg "127.19" xsd:float
-property_value: DiffFormula "C 7 H 13 N 1 O 1" xsd:string
-property_value: DiffMono "127.099714" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:60
-is_a: MOD:01426
-
-[Term]
-id: MOD:00454
-name: quaternary amine labeling reagent heavy form (+3amu) (N-term & K)
-def: "A protein modification that effectively replaces a residue alpha-amino- or alpha-imino-hydrogen with a quaternary amine reagent heavy (+3amu) form group." [PubMed:11857757, Unimod:61]
-synonym: "GIST-Quat:2H(3)" RELATED PSI-MS-label []
-synonym: "Quaternary amine labeling reagent heavy (+3amu) form, N-term & K" RELATED Unimod-description []
-property_value: DiffAvg "130.12" xsd:float
-property_value: DiffFormula "C 7 (1)H 10 (2)H 3 N 1 O 1" xsd:string
-property_value: DiffMono "130.118544" xsd:float
-property_value: Formula "C 13 (1)H 22 (2)H 3 N 3 O 2" xsd:string
-property_value: MassAvg "258.21" xsd:float
-property_value: MassMono "258.213507" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:61
-is_a: MOD:01426
-
-[Term]
-id: MOD:00455
-name: quaternary amine labeling reagent heavy form (+6amu) (N-term & K)
-def: "A protein modification that effectively replaces a residue alpha-amino- or alpha-imino-hydrogen with a quaternary amine reagent heavy (+6amu) form group." [PubMed:11857757, Unimod:62]
-synonym: "GIST-Quat:2H(6)" RELATED PSI-MS-label []
-synonym: "Quaternary amine labeling reagent heavy form (+6amu), N-term & K" RELATED Unimod-description []
-property_value: DiffAvg "133.14" xsd:float
-property_value: DiffFormula "C 7 H 7 (2)H 6 N 1 O 1" xsd:string
-property_value: DiffMono "133.137375" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:62
-is_a: MOD:01426
-
-[Term]
-id: MOD:00456
-name: quaternary amine labeling reagent heavy form (+9amu) (N-term & K)
-def: "A protein modification that effectively replaces a residue alpha-amino- or alpha-imino-hydrogen with a quaternary amine reagent heavy (+9amu) form group." [PubMed:11857757, Unimod:63]
-synonym: "GIST-Quat:2H(9)" RELATED PSI-MS-label []
-synonym: "Quaternary amine labeling reagent heavy form (+9amu), N-term & K" RELATED Unimod-description []
-property_value: DiffAvg "136.16" xsd:float
-property_value: DiffFormula "C 7 (1)H 4 (2)H 9 N 1 O 1" xsd:string
-property_value: DiffMono "136.156205" xsd:float
-property_value: Formula "C 13 (1)H 16 (2)H 9 N 3 O 2" xsd:string
-property_value: MassAvg "264.25" xsd:float
-property_value: MassMono "264.251168" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:63
-is_a: MOD:01426
-
-[Term]
-id: MOD:00457
-name: 4x(12)C, 4x(1)H labeled alpha-amino succinylated residue
-def: "A protein modification that effectively replaces a residue alpha-amino- or alpha-imino-hydrogen with a light succinyl group." [PubMed:11857757, PubMed:12175151, Unimod:64#N-term]
-synonym: "Succinic anhydride labeling reagent light form (N-term)" RELATED Unimod-description []
-synonym: "Succinyl" RELATED PSI-MS-label []
-property_value: DiffAvg "100.03" xsd:float
-property_value: DiffFormula "(12)C 4 (1)H 4 O 3" xsd:string
-property_value: DiffMono "100.016044" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:64
-relationship: derives_from MOD:01029
-is_a: MOD:01696
-is_a: MOD:01426
-
-[Term]
-id: MOD:00458
-name: 4x(2)H labeled alpha-amino succinylated residue
-def: "A protein modification that effectively replaces a residue alpha-amino- or alpha-imino-hydrogen with a 4x(2)H labeled succinyl group." [PubMed:11857757, PubMed:12175151, Unimod:65#N-term]
-synonym: "Succinic anhydride labeling reagent, heavy form (+4amu, 4H2), N-term" RELATED Unimod-description []
-synonym: "Succinyl:2H(4)" RELATED PSI-MS-label []
-property_value: DiffAvg "104.04" xsd:float
-property_value: DiffFormula "C 4 (2)H 4 O 3" xsd:string
-property_value: DiffMono "104.041151" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:65
-relationship: derives_from MOD:01029
-is_a: MOD:01696
-is_a: MOD:01426
-
-[Term]
-id: MOD:00459
-name: 4x(13)C labeled alpha-amino succinylated residue
-def: "A protein modification that effectively replaces a residue alpha-amino- or alpha-imino-hydrogen with a 4x(13)C labeled succinyl group." [PubMed:11857757, PubMed:12175151, Unimod:66#N-term]
-synonym: "Succinic anhydride labeling reagent, heavy form (+4amu, 4C13), N-term & K" RELATED Unimod-description []
-synonym: "Succinyl:13C(4)" RELATED PSI-MS-label []
-property_value: DiffAvg "104.03" xsd:float
-property_value: DiffFormula "(13)C 4 H 4 O 3" xsd:string
-property_value: DiffMono "104.029463" xsd:float
-property_value: Origin "X" xsd:string
-xref: Unimod:66
-relationship: derives_from MOD:01029
-is_a: MOD:01696
-is_a: MOD:01428
-is_a: MOD:01426
-
-[Term]
-id: MOD:00460
-name: L-cysteic acid (L-cysteine sulfonic acid)
-def: "A protein modification that effectively trioxygenates an L-cysteine residue to L-cysteine sulfonic acid." [ChEBI:17285, DeltaMass:334, OMSSA:34, PubMed:14678012, PubMed:18306178, PubMed:19522542, PubMed:9252331, RESID:AA0556, Unimod:345#C]
-comment: From DeltaMass: Notes:Treatment of cysteine by strongly oxidising reagents such as performic acid results in the complete oxidation of the sulphur atom. Such treatment is often carried out prior to amino acid analysis as the resulting cysteic acid is then resistant to acid degradation during the hydrolysis procedure.
-subset: PSI-MOD-slim
-synonym: "(2R)-2-amino-3-sulfopropanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-2-carboxyethanesulfonic acid" EXACT RESID-alternate []
-synonym: "2-azanyl-3-sulfopropanoic acid" EXACT RESID-alternate []
-synonym: "3-sulfoalanine" EXACT RESID-alternate []
-synonym: "Cya" EXACT DeltaMass-label []
-synonym: "CysO3H" EXACT PSI-MOD-label []
-synonym: "cysteic acid" EXACT RESID-alternate []
-synonym: "Cysteic acid, oxidation of cysteine" EXACT DeltaMass-label []
-synonym: "cysteicacidc" EXACT OMSSA-label []
-synonym: "cysteine oxidation to cysteic acid" RELATED Unimod-description []
-synonym: "cysteine sulphonic acid" EXACT RESID-alternate []
-synonym: "L-cysteine sulfonic acid" EXACT RESID-name []
-synonym: "Trioxidation" RELATED PSI-MS-label []
-synonym: "MOD_RES Cysteine sulfonic acid (-SO3H)" EXACT UniProt-feature []
-property_value: DiffAvg "48.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 3 S 0" xsd:string
-property_value: DiffMono "47.984744" xsd:float
-property_value: Formula "C 3 H 5 N 1 O 4 S 1" xsd:string
-property_value: MassAvg "151.14" xsd:float
-property_value: MassMono "150.993929" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:345
-xref: uniprot.ptm:PTM-0634
-is_a: MOD:00708
-
-[Term]
-id: MOD:00461
-name: nitrated residue
-def: "A protein modification that effectively substitutes a nitrite (NO2) group for a hydrogen atom." [DeltaMass:0, PubMed:8839040, PubMed:9252331, Unimod:354]
-comment: Note, this is often misrepresented as the introduction of a nitrate (NO3) group [JSG].
-subset: PSI-MOD-slim
-synonym: "Nitro" RELATED PSI-MS-label []
-synonym: "Nitro (NO2)" EXACT DeltaMass-label []
-synonym: "Oxidation to nitro" RELATED Unimod-description []
-property_value: DiffAvg "45.00" xsd:float
-property_value: DiffFormula "H -1 N 1 O 2" xsd:string
-property_value: DiffMono "44.985078" xsd:float
-property_value: Origin "X" xsd:string
-xref: Unimod:354
-is_a: MOD:00848
-
-[Term]
-id: MOD:00462
-name: L-kynurenine
-def: "A protein modification that effectively converts an L-tryptophan residue to L-kynurenine." [DeltaMass:357, OMSSA:66, PubMed:11029593, PubMed:9252331, Unimod:351#W]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-4-(2-aminophenyl)-4-oxo-butanoic acid" EXACT PSI-MOD-alternate []
-synonym: "kynureninw" EXACT OMSSA-label []
-synonym: "Trp->Kynurenin" RELATED PSI-MS-label []
-synonym: "tryptophan oxidation to kynurenin" RELATED Unimod-description []
-property_value: DiffAvg "3.99" xsd:float
-property_value: DiffFormula "C -1 O 1" xsd:string
-property_value: DiffMono "3.994915" xsd:float
-property_value: Formula "C 10 H 10 N 2 O 2" xsd:string
-property_value: MassAvg "190.20" xsd:float
-property_value: MassMono "190.074228" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:351
-is_a: MOD:00918
-
-[Term]
-id: MOD:00463
-name: 3'-hydroxy-L-kynurenine
-def: "A protein modification that effectively converts an L-tryptophan residue to 3'-hydroxy-L-kynurenine." [OMSSA:58, PubMed:9252331, Unimod:350#W]
-subset: PSI-MOD-slim
-synonym: "hydroxykynureninw" EXACT OMSSA-label []
-synonym: "Trp->Hydroxykynurenin" RELATED PSI-MS-label []
-synonym: "tryptophan oxidation to hydroxykynurenin" RELATED Unimod-description []
-property_value: DiffAvg "19.99" xsd:float
-property_value: DiffFormula "C -1 O 2" xsd:string
-property_value: DiffMono "19.989829" xsd:float
-property_value: Formula "C 10 H 10 N 2 O 3" xsd:string
-property_value: MassAvg "206.20" xsd:float
-property_value: MassMono "206.069142" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:350
-is_a: MOD:00679
-is_a: MOD:00918
-
-[Term]
-id: MOD:00464
-name: N'-formyl-L-kynurenine
-def: "A protein modification that effectively converts an L-tryptophan residue to N'-formyl-L-kynurenine." [DeltaMass:356, OMSSA:45, PubMed:12124932, PubMed:12686488, PubMed:9252331, Unimod:425#W]
-comment: From DeltaMass: References:Willy V. Bienvenut, Catherine Déon, Carla Pasquarello, Jennifer M. Campbell, Jean-Charles Sanchez, Marvin L. Vestal, Denis F. Hochstrasser Matrix-assisted laser desorption/ionization-tandemmass spectrometry with high resolution andsensitivity for identification and characterizationof proteins. Proteomics 2002, 2, 868-876 Notes: A double oxidation of tryptophan for which the N-formylkynurenine (+32) structure can be proposed. Many minor peaks accompanying the main peak might also be attributed to other oxidation products of the tryptophan such as kynurenine (+4), an unknown by-product found in all oxidized tryptophan patterns (+13), hydroxytryptophan (+16), 3-hydroxykynurenine (+20) and hydroxy-N-formylkynurenine (+48). See proposed structures at http://www.abrf.org/images/misc/dmass32.jpg.
-subset: PSI-MOD-slim
-synonym: "dihydroxy" RELATED Unimod-description []
-synonym: "Dioxidation" RELATED PSI-MS-label []
-synonym: "Double oxidation of Trp" EXACT DeltaMass-label []
-synonym: "formylkynureninw" EXACT OMSSA-label []
-synonym: "tryptophan oxidation to formylkynurenin" RELATED Unimod-alternate []
-property_value: DiffAvg "32.00" xsd:float
-property_value: DiffFormula "O 2" xsd:string
-property_value: DiffMono "31.989829" xsd:float
-property_value: Formula "C 11 H 10 N 2 O 3" xsd:string
-property_value: MassAvg "218.21" xsd:float
-property_value: MassMono "218.069142" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:425
-is_a: MOD:00679
-is_a: MOD:00918
-
-[Term]
-id: MOD:00465
-name: dihydroxyphenylalanine (Phe)
-def: "A protein modification that effectively converts an L-phenylalanine residue to a dihydroxyphenylalanine." [OMSSA:39, PubMed:1610822, PubMed:1903612, PubMed:3734192, PubMed:9252331, RESID:AA0146#var, Unimod:425#F]
-comment: Dihydroxyphenyalanines with a 4'-hydroxyl orginate naturally by a monohydroxylation of tyrosine, and not by dihydroxylation of phenylalanine [JSG].
-subset: PSI-MOD-slim
-synonym: "dihydroxy" RELATED Unimod-description []
-synonym: "dihydroxyf" EXACT OMSSA-label []
-synonym: "Dioxidation" RELATED PSI-MS-label []
-property_value: DiffAvg "32.00" xsd:float
-property_value: DiffFormula "O 2" xsd:string
-property_value: DiffMono "31.989829" xsd:float
-property_value: Formula "C 9 H 9 N 1 O 3" xsd:string
-property_value: MassAvg "179.17" xsd:float
-property_value: MassMono "179.058243" xsd:float
-property_value: Origin "F" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:425
-is_a: MOD:00428
-is_a: MOD:00914
-
-[Term]
-id: MOD:00466
-name: glycosylsphingolipidinositolated residue
-def: "A protein modification that effectively converts a residue to a glycosylsphingolipidinositolethanolamidated." [PubMed:12626404, PubMed:18688235, PubMed:8404891]
-synonym: "GSIRes" EXACT PSI-MOD-label []
-is_a: MOD:00764
-is_a: MOD:01155
-
-[Term]
-id: MOD:00467
-name: iminobiotinyl modified residue
-def: "A protein modification that effectively substitutes an iminobiotinyl group for a hydrogen atom." [PubMed:9750125, Unimod:89]
-synonym: "Iminobiotin" RELATED PSI-MS-label []
-synonym: "Iminobiotinylation" RELATED Unimod-description []
-property_value: DiffAvg "225.31" xsd:float
-property_value: DiffFormula "C 10 H 15 N 3 O 1 S 1" xsd:string
-property_value: DiffMono "225.093583" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:89
-is_a: MOD:00848
-
-[Term]
-id: MOD:00468
-name: ESP-Tag light d0
-def: "modification from Unimod Isotopic label" [Unimod:90]
-synonym: "ESP" RELATED PSI-MS-label []
-synonym: "ESP-Tag light d0" RELATED Unimod-description []
-property_value: DiffAvg "338.47" xsd:float
-property_value: DiffFormula "C 16 H 26 N 4 O 2 S 1" xsd:string
-property_value: DiffMono "338.177647" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:90
-is_a: MOD:01426
-
-[Term]
-id: MOD:00469
-name: ESP-Tag heavy d10
-def: "modification from Unimod Isotopic label" [Unimod:91]
-synonym: "ESP-Tag heavy d10" RELATED Unimod-description []
-synonym: "ESP:2H(10)" RELATED PSI-MS-label []
-property_value: DiffAvg "348.24" xsd:float
-property_value: DiffFormula "C 16 (1)H 16 (2)H 10 N 4 O 2 S 1" xsd:string
-property_value: DiffMono "348.240415" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:91
-is_a: MOD:01431
-
-[Term]
-id: MOD:00470
-name: NHS-LC-Biotin
-def: "modification from Unimod Chemical derivative" [Unimod:92]
-synonym: "NHS-LC-Biotin" RELATED Unimod-interim []
-synonym: "NHS-LC-Biotin" RELATED Unimod-description []
-property_value: DiffAvg "339.45" xsd:float
-property_value: DiffFormula "C 16 H 25 N 3 O 3 S 1" xsd:string
-property_value: DiffMono "339.161663" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:92
-is_a: MOD:00848
-
-[Term]
-id: MOD:00471
-name: EDT-maleimide-PEO-biotin
-def: "modification from Unimod Chemical derivative" [Unimod:93]
-synonym: "EDT-maleimide-PEO-biotin" RELATED Unimod-interim []
-synonym: "EDT-maleimide-PEO-biotin" RELATED Unimod-description []
-property_value: DiffAvg "601.80" xsd:float
-property_value: DiffFormula "C 25 H 39 N 5 O 6 S 3" xsd:string
-property_value: DiffMono "601.206247" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:93
-is_a: MOD:00848
-
-[Term]
-id: MOD:00472
-name: IMID d0
-def: "modification from Unimod Isotopic label" [PubMed:11746907, Unimod:94, URL:http\://dx.doi.org/10.1002/rcm.517]
-synonym: "IMID" RELATED PSI-MS-label []
-synonym: "IMID d0" RELATED Unimod-description []
-property_value: DiffAvg "68.04" xsd:float
-property_value: DiffFormula "C 3 (1)H 4 N 2" xsd:string
-property_value: DiffMono "68.037448" xsd:float
-property_value: Formula "C 9 H 16 N 4 O 1" xsd:string
-property_value: MassAvg "196.13" xsd:float
-property_value: MassMono "196.132411" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:94
-is_a: MOD:01426
-
-[Term]
-id: MOD:00473
-name: IMID d4
-def: "modification from Unimod Isotopic label" [PubMed:11746907, Unimod:95, URL:http\://dx.doi.org/10.1002/rcm.517]
-synonym: "IMID d4" RELATED Unimod-description []
-synonym: "IMID:2H(4)" RELATED PSI-MS-label []
-property_value: DiffAvg "72.06" xsd:float
-property_value: DiffFormula "C 3 (2)H 4 N 2" xsd:string
-property_value: DiffMono "72.062555" xsd:float
-property_value: Formula "C 9 (1)H 12 (2)H 4 N 4 O 1" xsd:string
-property_value: MassAvg "200.16" xsd:float
-property_value: MassMono "200.157518" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:95
-is_a: MOD:01426
-
-[Term]
-id: MOD:00474
-name: S-([1,1,2-(2)H3]-carboxamidoethyl)-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-(1,1,2-(2)H3)-propanamide-L-cysteine." [Unimod:97#C]
-synonym: "Acrylamide d3" RELATED Unimod-description []
-synonym: "Propionamide:2H(3)" RELATED PSI-MS-label []
-synonym: "S-([1,1,2-(2)H3]-3-amino-3-oxopropyl)cysteine" EXACT PSI-MOD-alternate []
-synonym: "S-([1,1,2-(2)H3]-carbamoylethyl)-L-cysteine" EXACT PSI-MOD-alternate []
-synonym: "S-([1,1,2-(2)H3]-propanamide)-L-cysteine" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "74.06" xsd:float
-property_value: DiffFormula "C 3 (1)H 2 (2)H 3 N 1 O 1" xsd:string
-property_value: DiffMono "74.055944" xsd:float
-property_value: Formula "C 6 (1)H 7 (2)H 3 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "177.07" xsd:float
-property_value: MassMono "177.065129" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:97
-relationship: derives_from MOD:00417
-is_a: MOD:01426
-
-[Term]
-id: MOD:00475
-name: 2-amino-L-tyrosine
-def: "A protein modification that effectively converts an L-tyrosine residue to 2-amino-L-tyrosine." [PubMed:8839040, PubMed:9252331, Unimod:342#Y]
-synonym: "Amino" RELATED PSI-MS-label []
-synonym: "Tyrosine oxidation to 2-aminotyrosine" RELATED Unimod-description []
-property_value: DiffAvg "15.02" xsd:float
-property_value: DiffFormula "H 1 N 1" xsd:string
-property_value: DiffMono "15.010899" xsd:float
-property_value: Formula "C 9 H 10 N 2 O 2" xsd:string
-property_value: MassAvg "178.19" xsd:float
-property_value: MassMono "178.074228" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:342
-is_a: MOD:00919
-is_a: MOD:02039
-
-[Term]
-id: MOD:00476
-name: monogalactosylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with an galactose group through a glycosidic bond." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "GalRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "162.14" xsd:float
-property_value: DiffFormula "C 6 H 10 O 5" xsd:string
-property_value: DiffMono "162.052823" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00761
-is_a: MOD:00728
-
-[Term]
-id: MOD:00477
-name: 2-pyrrolidone
-def: "A protein modification that effectively converts, by oxidative decarboxylation, an L-proline residue to 2-pyrrolidone with breakage of the peptide chain." [PubMed:2161657, PubMed:9252331, Unimod:360#P]
-comment: The oxidative decarboxylation of a proline residue results in breaking of the peptide chain, leaving a peptidyl-2-pyrrolidone at the C-terminus. The difference formula, derived from the result in the original citation, has been corrected from the Unimod entry.
-synonym: "Pro->Pyrrolidinone" RELATED PSI-MS-label []
-synonym: "Proline oxidation to pyrrolidinone" RELATED Unimod-description []
-property_value: DiffAvg "-13.02" xsd:float
-property_value: DiffFormula "C -1 H -1 N 0 O 0" xsd:string
-property_value: DiffMono "-13.007825" xsd:float
-property_value: Formula "C 4 H 6 N 1 O 1" xsd:string
-property_value: MassAvg "84.10" xsd:float
-property_value: MassMono "84.044939" xsd:float
-property_value: Origin "P" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:360
-is_a: MOD:00683
-is_a: MOD:00915
-
-[Term]
-id: MOD:00478
-name: glutamyl semialdehyde (Pro)
-def: "A protein modification that effectively converts an L-proline residue to L-glutamyl semialdehyde." [DeltaMass:354, PubMed:11120890, PubMed:2563380, PubMed:9252331, Unimod:35#P]
-synonym: "gamma-glutamyl semialdehyde" EXACT PSI-MOD-alternate []
-synonym: "glutamyl 5-semialdehyde" EXACT PSI-MOD-alternate []
-synonym: "glutamyl aldehyde" EXACT PSI-MOD-alternate []
-synonym: "Oxidation" RELATED Unimod-interim []
-synonym: "Oxidation of proline to gamma-glutamyl semialdehyde" EXACT DeltaMass-label []
-synonym: "Oxidation or Hydroxylation" RELATED Unimod-description []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 5 H 7 N 1 O 2" xsd:string
-property_value: MassAvg "113.12" xsd:float
-property_value: MassMono "113.047678" xsd:float
-property_value: Origin "P" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:35
-is_a: MOD:00679
-is_a: MOD:00915
-is_a: MOD:01440
-
-[Term]
-id: MOD:00479
-name: glutamyl semialdehyde (Arg)
-def: "A protein modification that effectively converts an L-arginine residue to L-glutamyl semialdehyde." [DeltaMass:351, PubMed:11120890, PubMed:1680314, PubMed:9252331, Unimod:344#R]
-comment: From DeltaMass: Average Mass: -27 Monoisotopic Mass Change:-27.06 Average Mass Change:-27.07 References:Amici A, Levine, RL, Tsai, L, and Stadtman, ER: Conversion of amino acid residues in proteins and amino acid homopolymers to carbonyl derivatives by metal-catalyzed oxidation reactions. Journal of Biological Chemistry 264: 3341-3346 1989.Requena JR, Chao CC, Levine RL, and Stadtman ER: Glutamic and aminoadipic semialdehydes are the main carbonyl products of metal-catalyzed oxidation of proteins. Proceedings of the National Academy of Sciences USA 98: 69-74 2001.
-synonym: "Arg->GluSA" RELATED PSI-MS-label []
-synonym: "Arginine oxidation to glutamic semialdehyde" RELATED Unimod-description []
-synonym: "Oxidation of arginine (to glutamic acid)" EXACT DeltaMass-label []
-property_value: DiffAvg "-43.07" xsd:float
-property_value: DiffFormula "C -1 H -5 N -3 O 1" xsd:string
-property_value: DiffMono "-43.053433" xsd:float
-property_value: Formula "C 5 H 7 N 1 O 2" xsd:string
-property_value: MassAvg "113.12" xsd:float
-property_value: MassMono "113.047678" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:344
-is_a: MOD:00902
-is_a: MOD:01440
-
-[Term]
-id: MOD:00480
-name: Applied Biosystems cleavable ICAT(TM) light
-def: "modification from Unimod Isotopic label" [OMSSA:129, Unimod:105#C, URL:http\://www.appliedbiosystems.com/products/productdetail.cfm?prod_id=153]
-subset: PSI-MOD-slim
-synonym: "Applied Biosystems cleavable ICAT(TM) light" RELATED Unimod-description []
-synonym: "ICAT-C" RELATED PSI-MS-label []
-synonym: "icatlight" EXACT OMSSA-label []
-property_value: DiffAvg "227.26" xsd:float
-property_value: DiffFormula "C 10 H 17 N 3 O 3" xsd:string
-property_value: DiffMono "227.126991" xsd:float
-property_value: Formula "C 13 H 22 N 4 O 4 S 1" xsd:string
-property_value: MassAvg "330.40" xsd:float
-property_value: MassMono "330.136176" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:105
-is_a: MOD:01426
-
-[Term]
-id: MOD:00481
-name: Applied Biosystems cleavable ICAT(TM) heavy
-def: "modification from Unimod Isotopic label" [OMSSA:130, Unimod:106#C, URL:http\://www.appliedbiosystems.com/products/productdetail.cfm?prod_id=153]
-subset: PSI-MOD-slim
-synonym: "Applied Biosystems cleavable ICAT(TM) heavy" RELATED Unimod-description []
-synonym: "ICAT-C:13C(9)" RELATED PSI-MS-label []
-synonym: "icatheavy" EXACT OMSSA-label []
-property_value: DiffAvg "236.16" xsd:float
-property_value: DiffFormula "(12)C 1 (13)C 9 H 17 N 3 O 3" xsd:string
-property_value: DiffMono "236.157185" xsd:float
-property_value: Formula "(12)C 4 (13)C 9 H 22 N 4 O 4 S 1" xsd:string
-property_value: MassAvg "339.17" xsd:float
-property_value: MassMono "339.166370" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:106
-is_a: MOD:01428
-
-[Term]
-id: MOD:00482
-name: N-formyl-L-methionine (Met)
-def: "A protein modification that effectively converts an L-methionine residue to N-formyl-L-methionine (not known as a natural, post-translational modification process)." [PubMed:11152118, PubMed:2165784, PubMed:3042771, Unimod:122#M, RESID:AA0021#MET]
-comment: This entry is for the artifactual formation of N-formyl-L-methionine from methionine. For encoded N-formyl-L-methionine, use MOD:00030 [JSG].
-synonym: "(2S)-2-formylamino-4-(methylsulfanyl)butanoic acid" EXACT RESID-systematic []
-synonym: "2-formamido-4-(methylsulfanyl)butanoic acid" EXACT RESID-alternate []
-synonym: "2-formylamino-4-(methylthio)butanoic acid" EXACT RESID-alternate []
-synonym: "2-formylazanyl-4-(methylsulfanyl)butanoic acid" EXACT RESID-alternate []
-synonym: "MOD_RES N-formylmethionine" EXACT UniProt-feature []
-synonym: "N-formyl-L-methionine" EXACT RESID-name []
-synonym: "N-formylated L-methionine" EXACT PSI-MOD-alternate []
-synonym: "NFoMet" EXACT PSI-MOD-label []
-property_value: DiffAvg "28.01" xsd:float
-property_value: DiffFormula "C 1 H 0 N 0 O 1 S 0" xsd:string
-property_value: DiffMono "27.994915" xsd:float
-property_value: Formula "C 6 H 10 N 1 O 2 S 1" xsd:string
-property_value: MassAvg "160.21" xsd:float
-property_value: MassMono "160.043225" xsd:float
-property_value: Origin "M" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:122
-xref: uniprot.ptm:PTM-0212
-is_a: MOD:00913
-
-[Term]
-id: MOD:00483
-name: N-ethylmaleimide derivatized cysteine
-def: "A protein modification that is produced by reaction with N-ethylmaleimide." [OMSSA:83, PubMed:11813307, PubMed:12777388, Unimod:108#C]
-synonym: "N-ethylmaleimide on cysteines" RELATED Unimod-description []
-synonym: "nemc" EXACT OMSSA-label []
-synonym: "Nethylmaleimide" RELATED PSI-MS-label []
-property_value: DiffAvg "125.13" xsd:float
-property_value: DiffFormula "C 6 H 7 N 1 O 2" xsd:string
-property_value: DiffMono "125.047678" xsd:float
-property_value: Formula "C 9 H 12 N 2 O 3 S 1" xsd:string
-property_value: MassAvg "228.27" xsd:float
-property_value: MassMono "228.056863" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:108
-is_a: MOD:00848
-is_a: MOD:00905
-
-[Term]
-id: MOD:00484
-name: oxidized lysine biotinylated with biotin-LC-hydrazide, reduced
-def: "modification from Unimod Chemical derivative" [Unimod:112#K]
-synonym: "Oxidized lysine biotinylated with biotin-LC-hydrazide, reduced" RELATED Unimod-description []
-synonym: "OxLysBiotinRed" RELATED Unimod-interim []
-property_value: DiffAvg "354.47" xsd:float
-property_value: DiffFormula "C 16 H 26 N 4 O 3 S 1" xsd:string
-property_value: DiffMono "354.172562" xsd:float
-property_value: Formula "C 22 H 38 N 6 O 4 S 1" xsd:string
-property_value: MassAvg "482.64" xsd:float
-property_value: MassMono "482.267525" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:112
-is_a: MOD:00848
-is_a: MOD:00912
-
-[Term]
-id: MOD:00485
-name: oxidized lysine biotinylated with biotin-LC-hydrazide
-def: "modification from Unimod Chemical derivative" [Unimod:113#K]
-synonym: "Oxidized lysine biotinylated with biotin-LC-hydrazide" RELATED Unimod-description []
-synonym: "OxLysBiotin" RELATED Unimod-interim []
-property_value: DiffAvg "352.45" xsd:float
-property_value: DiffFormula "C 16 H 24 N 4 O 3 S 1" xsd:string
-property_value: DiffMono "352.156912" xsd:float
-property_value: Formula "C 22 H 36 N 6 O 4 S 1" xsd:string
-property_value: MassAvg "480.63" xsd:float
-property_value: MassMono "480.251875" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:113
-is_a: MOD:00848
-is_a: MOD:00912
-
-[Term]
-id: MOD:00486
-name: oxidized proline biotinylated with biotin-LC-hydrazide, reduced
-def: "modification from Unimod Chemical derivative" [Unimod:114#C]
-synonym: "Oxidized proline biotinylated with biotin-LC-hydrazide, reduced" RELATED Unimod-description []
-synonym: "OxProBiotinRed" RELATED Unimod-interim []
-property_value: DiffAvg "371.50" xsd:float
-property_value: DiffFormula "C 16 H 29 N 5 O 3 S 1" xsd:string
-property_value: DiffMono "371.199111" xsd:float
-property_value: Formula "C 21 H 36 N 6 O 4 S 1" xsd:string
-property_value: MassAvg "468.62" xsd:float
-property_value: MassMono "468.251875" xsd:float
-property_value: Origin "P" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:114
-is_a: MOD:00848
-is_a: MOD:00915
-
-[Term]
-id: MOD:00487
-name: oxidized proline biotinylated with biotin-LC-hydrazide
-def: "modification from Unimod Chemical derivative" [Unimod:115#C]
-synonym: "Oxidized Proline biotinylated with biotin-LC-hydrazide" RELATED Unimod-description []
-synonym: "OxProBiotin" RELATED Unimod-interim []
-property_value: DiffAvg "369.48" xsd:float
-property_value: DiffFormula "C 16 H 27 N 5 O 3 S 1" xsd:string
-property_value: DiffMono "369.183461" xsd:float
-property_value: Formula "C 21 H 34 N 6 O 4 S 1" xsd:string
-property_value: MassAvg "466.60" xsd:float
-property_value: MassMono "466.236225" xsd:float
-property_value: Origin "P" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:115
-is_a: MOD:00848
-is_a: MOD:00915
-
-[Term]
-id: MOD:00488
-name: oxidized arginine biotinylated with biotin-LC-hydrazide
-def: "modification from Unimod Chemical derivative" [Unimod:116#C]
-synonym: "OxArgBiotin" RELATED Unimod-interim []
-synonym: "Oxidized arginine biotinylated with biotin-LC-hydrazide" RELATED Unimod-description []
-property_value: DiffAvg "310.41" xsd:float
-property_value: DiffFormula "C 15 H 22 N 2 O 3 S 1" xsd:string
-property_value: DiffMono "310.135114" xsd:float
-property_value: Formula "C 21 H 34 N 6 O 4 S 1" xsd:string
-property_value: MassAvg "466.60" xsd:float
-property_value: MassMono "466.236225" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-is_a: MOD:00902
-
-[Term]
-id: MOD:00489
-name: oxidized arginine biotinylated with biotin-LC-hydrazide, reduced
-def: "modification from Unimod Chemical derivative" [Unimod:117#C]
-synonym: "OxArgBiotinRed" RELATED Unimod-interim []
-synonym: "Oxidized arginine biotinylated with biotin-LC-hydrazide, reduced" RELATED Unimod-description []
-property_value: DiffAvg "312.43" xsd:float
-property_value: DiffFormula "C 15 H 24 N 2 O 3 S 1" xsd:string
-property_value: DiffMono "312.150764" xsd:float
-property_value: Formula "C 21 H 36 N 6 O 4 S 1" xsd:string
-property_value: MassAvg "468.62" xsd:float
-property_value: MassMono "468.251875" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:117
-is_a: MOD:00848
-is_a: MOD:00902
-
-[Term]
-id: MOD:00490
-name: EDT-iodo-PEO-biotin
-def: "modification from Unimod Chemical derivative" [Unimod:118]
-synonym: "EDT-iodo-PEO-biotin" RELATED Unimod-description []
-synonym: "EDT-iodoacetyl-PEO-biotin" RELATED PSI-MS-label []
-property_value: DiffAvg "490.70" xsd:float
-property_value: DiffFormula "C 20 H 34 N 4 O 4 S 3" xsd:string
-property_value: DiffMono "490.174219" xsd:float
-property_value: Origin "X" xsd:string
-xref: Unimod:118
-is_a: MOD:00848
-
-[Term]
-id: MOD:00491
-name: thio ether formation - BTP Adduct
-def: "modification from Unimod Chemical derivative" [PubMed:11861642, Unimod:119#C]
-synonym: "IBTP" RELATED PSI-MS-label []
-synonym: "Thio Ether Formation - BTP Adduct" RELATED Unimod-description []
-property_value: DiffAvg "316.38" xsd:float
-property_value: DiffFormula "C 22 H 21 P 1" xsd:string
-property_value: DiffMono "316.138087" xsd:float
-property_value: Formula "C 25 H 26 N 1 O 1 P 1 S 1" xsd:string
-property_value: MassAvg "419.52" xsd:float
-property_value: MassMono "419.147272" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:119
-is_a: MOD:00848
-is_a: MOD:00861
-is_a: MOD:00905
-
-[Term]
-id: MOD:00492
-name: ubiquitination signature dipeptidyl lysine
-def: "A protein modification that crosslinks the N6-amino of a peptidyl lysine with the carboxyl of glycylglycine, the two glycine residues left after tryptic digestion of ubiquitin." [OMSSA:52, PubMed:11125103, PubMed:12612601, PubMed:12872131, RESID:AA0125#var, Unimod:121#K]
-synonym: "GlyGly" RELATED PSI-MS-label []
-synonym: "glyglyk" EXACT OMSSA-label []
-synonym: "N6-(glycylglycyl)lysine" EXACT PSI-MOD-alternate []
-synonym: "N6-glycylglycyl-L-lysine" EXACT PSI-MOD-alternate []
-synonym: "ubiquitinylation residue" RELATED Unimod-description []
-property_value: DiffAvg "114.10" xsd:float
-property_value: DiffFormula "C 4 H 6 N 2 O 2" xsd:string
-property_value: DiffMono "114.042927" xsd:float
-property_value: Formula "C 10 H 18 N 4 O 3" xsd:string
-property_value: MassAvg "242.28" xsd:float
-property_value: MassMono "242.137890" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:121
-is_a: MOD:02047
-is_a: MOD:02051
-is_a: MOD:01875
-relationship: derives_from MOD:01148
-
-[Term]
-id: MOD:00493
-name: formylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with a formyl group." [DeltaMass:0, PubMed:15799070, Unimod:122]
-comment: From DeltaMass: Average Mass: 28
-subset: PSI-MOD-slim
-synonym: "FoRes" EXACT PSI-MOD-label []
-synonym: "Formyl" RELATED PSI-MS-label []
-synonym: "Formylation" RELATED Unimod-description []
-synonym: "Formylation (CHO)" EXACT DeltaMass-label []
-property_value: DiffAvg "28.01" xsd:float
-property_value: DiffFormula "C 1 O 1" xsd:string
-property_value: DiffMono "27.994915" xsd:float
-property_value: Origin "X" xsd:string
-xref: Unimod:122
-is_a: MOD:00649
-
-[Term]
-id: MOD:00494
-name: N-iodoacetyl, p-chlorobenzyl-12C6-glucamine
-def: "modification from Unimod Isotopic label" [PubMed:12185208, Unimod:123#C]
-synonym: "ICAT-H" RELATED PSI-MS-label []
-synonym: "N-iodoacetyl, p-chlorobenzyl-12C6-glucamine" RELATED Unimod-description []
-property_value: DiffAvg "345.78" xsd:float
-property_value: DiffFormula "C 15 Cl 1 H 20 N 1 O 6 S 0" xsd:string
-property_value: DiffMono "345.097915" xsd:float
-property_value: Formula "C 18 Cl 1 H 25 N 2 O 7 S 1" xsd:string
-property_value: MassAvg "448.91" xsd:float
-property_value: MassMono "448.107100" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:123
-is_a: MOD:00905
-is_a: MOD:01426
-
-[Term]
-id: MOD:00495
-name: N-iodoacetyl, p-chlorobenzyl-13C6-glucamine
-def: "modification from Unimod Isotopic label" [PubMed:12185208, Unimod:124#C]
-synonym: "ICAT-H:13C(6)" RELATED PSI-MS-label []
-synonym: "N-iodoacetyl, p-chlorobenzyl-13C6-glucamine" RELATED Unimod-description []
-property_value: DiffAvg "351.12" xsd:float
-property_value: DiffFormula "(12)C 9 (13)C 6 Cl 1 H 20 N 1 O 6 S 0" xsd:string
-property_value: DiffMono "351.118044" xsd:float
-property_value: Formula "(12)C 12 (13)C 6 Cl 1 H 25 N 2 O 7 S 1" xsd:string
-property_value: MassAvg "454.13" xsd:float
-property_value: MassMono "454.127229" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:124
-is_a: MOD:00905
-is_a: MOD:01426
-
-[Term]
-id: MOD:00496
-name: reductive amination-D
-def: "OBSOLETE because Unimod entry 125 is merged with entry 199, remap to id: MOD:00552" [Unimod:125]
-property_value: DiffAvg "32.06" xsd:float
-property_value: DiffFormula "C 2 (2)H 4" xsd:string
-property_value: DiffMono "32.056407" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-replaced_by: MOD:00552
-xref: Unimod:125
-is_obsolete: true
-
-[Term]
-id: MOD:00497
-name: 3-sulfanylpropanoyl (N-term and Lys)
-def: "modification from Unimod [(35)S]dithiobis(succinimidyl propionate) crosslinking" [PubMed:957432, Unimod:126]
-comment: The name \"thioacylation of primary amines\" in Unimod was a misdescription [JSG].
-synonym: "3,3-Dithio-bis-(sulfosuccinimidyl)propionate" RELATED Unimod-alternate []
-synonym: "3-sulfanylpropanoyl" RELATED Unimod-description []
-synonym: "Thioacyl" RELATED PSI-MS-label []
-property_value: DiffAvg "88.12" xsd:float
-property_value: DiffFormula "C 3 H 4 O 1 S 1" xsd:string
-property_value: DiffMono "87.998286" xsd:float
-property_value: Formula "C 9 H 16 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "216.30" xsd:float
-property_value: MassMono "216.093249" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:126
-is_a: MOD:00848
-is_a: MOD:00912
-
-[Term]
-id: MOD:00498
-name: fluorinated residue
-def: "A protein modification that effectively substitutes a hydrogen of a residue with a fluorine atom." [PubMed:18688235]
-synonym: "Fluoro" RELATED PSI-MS-label []
-synonym: "fluorophenylalanine replacement of phenylalanine" RELATED Unimod-description []
-synonym: "Fluorophenylalanyl" EXACT DeltaMass-label []
-synonym: "FRes" EXACT PSI-MOD-label []
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00694
-
-[Term]
-id: MOD:00499
-name: 5-iodoacetamidofluorescein
-def: "modification from Unimod Chemical derivative" [PubMed:3311742, PubMed:3578767, Unimod:128#C]
-synonym: "5-Iodoacetamidofluorescein (Molecular Probe, Eugene, OR)" RELATED Unimod-description []
-synonym: "Fluorescein" RELATED PSI-MS-label []
-property_value: DiffAvg "388.35" xsd:float
-property_value: DiffFormula "C 22 H 14 N 1 O 6" xsd:string
-property_value: DiffMono "388.082112" xsd:float
-property_value: Formula "C 25 H 19 N 2 O 7 S 1" xsd:string
-property_value: MassAvg "491.49" xsd:float
-property_value: MassMono "491.091297" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:128
-is_a: MOD:00848
-is_a: MOD:00905
-
-[Term]
-id: MOD:00500
-name: monoiodinated residue
-def: "A protein modification that effectively substitutes one hydrogen atom of a residue with one iodine atom." [DeltaMass:0, PubMed:15627961, PubMed:2026710, Unimod:129]
-comment: From DeltaMass: Average Mass: 126
-subset: PSI-MOD-slim
-synonym: "I1Res" EXACT PSI-MOD-label []
-synonym: "Iodination" RELATED Unimod-description []
-synonym: "Iodination (of Histidine[C4] or Tyrosine[C3])" EXACT DeltaMass-label []
-synonym: "Iodo" RELATED PSI-MS-label []
-property_value: DiffAvg "125.90" xsd:float
-property_value: DiffFormula "H -1 I 1" xsd:string
-property_value: DiffMono "125.896648" xsd:float
-property_value: Origin "X" xsd:string
-xref: Unimod:129
-is_a: MOD:00755
-
-[Term]
-id: MOD:00501
-name: diiodinated residue
-def: "A protein modification that effectively substitutes two hydrogen atoms of a residue with two iodine atoms." [Unimod:130]
-comment: From DeltaMass: Average Mass: 252
-subset: PSI-MOD-slim
-synonym: "di-Iodination" RELATED Unimod-description []
-synonym: "Diiodo" RELATED PSI-MS-label []
-synonym: "I2Res" EXACT PSI-MOD-label []
-property_value: DiffAvg "251.79" xsd:float
-property_value: DiffFormula "H -2 I 2" xsd:string
-property_value: DiffMono "251.793295" xsd:float
-property_value: Origin "X" xsd:string
-xref: Unimod:130
-is_a: MOD:00755
-
-[Term]
-id: MOD:00502
-name: triiodinated residue
-def: "A protein modification that effectively substitutes three hydrogen atoms of a residue with three iodine atoms." [OMSSA:116, PubMed:15627961, PubMed:2026710, Unimod:131]
-comment: From Unimod. In PubMed:2026710, mono- and diiodination of tyrosine are discussed, but triiodination of tyrosine is not mentioned. In PubMed:15627961, triiodothyronine (see MOD:00186) is discussed, but triiodotyrosine is not mentioned. This modification probably does not exist, and may be a confusion of \"tyrosine\" for \"thyronine\", a common error [JSG].
-subset: PSI-MOD-slim
-synonym: "I3Res" EXACT PSI-MOD-label []
-synonym: "tri-Iodination" RELATED Unimod-description []
-synonym: "triiodinationy" EXACT OMSSA-label []
-synonym: "Triiodo" RELATED PSI-MS-label []
-property_value: DiffAvg "377.69" xsd:float
-property_value: DiffFormula "H -3 I 3" xsd:string
-property_value: DiffMono "377.689943" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:131
-is_a: MOD:00755
-
-[Term]
-id: MOD:00503
-name: N-(cis-delta 5)-tetradecaenoylglycine
-def: "A protein modification that effectively converts a glycine residue to N-(cis-delta 5)-tetradecaenoylglycine." [OMSSA:78, PubMed:11955007, PubMed:11955008, PubMed:1326520, PubMed:1386601, PubMed:6436247, PubMed:7543369, RESID:AA0059#var, Unimod:134#G]
-synonym: "(cis-delta 5)-tetradecaenoyl" RELATED Unimod-description []
-synonym: "Myristoleyl" RELATED PSI-MS-label []
-synonym: "myristoleylation (one double bond)" EXACT DeltaMass-label []
-synonym: "N-(C14:1 aliphatic acyl)glycine" EXACT PSI-MOD-alternate []
-synonym: "ntermpepmyristoyeylationg" EXACT OMSSA-label []
-property_value: DiffAvg "208.35" xsd:float
-property_value: DiffFormula "C 14 H 24 N 0 O 1" xsd:string
-property_value: DiffMono "208.182715" xsd:float
-property_value: Formula "C 16 H 27 N 1 O 2" xsd:string
-property_value: MassAvg "265.40" xsd:float
-property_value: MassMono "265.204179" xsd:float
-property_value: Origin "G" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:134
-is_a: MOD:00908
-is_a: MOD:01696
-
-[Term]
-id: MOD:00504
-name: N-(cis,cis-delta 5,delta 8)-tetradecadienoylglycine
-def: "A protein modification that effectively converts a glycine residue to N-(cis,cis-delta 5,delta 8)-tetradecadienoylglycine." [OMSSA:79, PubMed:11955007, PubMed:11955008, PubMed:1326520, PubMed:1386601, PubMed:6436247, PubMed:7543369, RESID:AA0059#var, Unimod:135#G]
-synonym: "(cis,cis-delta 5, delta 8)-tetradecadienoyl" RELATED Unimod-description []
-synonym: "Myristoyl+Delta:H(-4)" RELATED PSI-MS-label []
-synonym: "myristoylation-4H (two double bonds)" EXACT DeltaMass-label []
-synonym: "N-(C14:2 aliphatic acyl)glycine" EXACT PSI-MOD-alternate []
-synonym: "ntermpepmyristoyl4hg" EXACT OMSSA-label []
-property_value: DiffAvg "206.33" xsd:float
-property_value: DiffFormula "C 14 H 22 O 1" xsd:string
-property_value: DiffMono "206.167065" xsd:float
-property_value: Formula "C 16 H 25 N 1 O 2" xsd:string
-property_value: MassAvg "263.38" xsd:float
-property_value: MassMono "263.188529" xsd:float
-property_value: Origin "G" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:135
-is_a: MOD:00908
-is_a: MOD:01696
-
-[Term]
-id: MOD:00505
-name: benzoyl labeling reagent light form (N-term and K)
-def: "modification from Unimod Isotopic label" [DeltaMass:0, PubMed:15456300, Unimod:136]
-comment: From DeltaMass: Average Mass: 104
-synonym: "Benzoyl" RELATED PSI-MS-label []
-synonym: "Benzoyl (Bz)" EXACT DeltaMass-label []
-synonym: "labeling reagent light form (N-term & K)" RELATED Unimod-description []
-property_value: DiffAvg "104.11" xsd:float
-property_value: DiffFormula "C 7 H 4 O 1" xsd:string
-property_value: DiffMono "104.026215" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:136
-is_a: MOD:00848
-
-[Term]
-id: MOD:00506
-name: N-linked glycan core N4-glycosylated asparagine
-def: "modification from Unimod N-linked glycosylation, Hex(5) HexNAc(2)" [PubMed:111247, PubMed:1694179, PubMed:5490222, RESID:AA0151#var, Unimod:137#N]
-synonym: "Hex(5)HexNAc(2)" RELATED PSI-MS-label []
-synonym: "N-linked glycan core" RELATED Unimod-description []
-property_value: DiffAvg "1217.09" xsd:float
-property_value: DiffFormula "C 46 H 76 N 2 O 35" xsd:string
-property_value: DiffMono "1216.422862" xsd:float
-property_value: Formula "C 50 H 82 N 4 O 37" xsd:string
-property_value: MassAvg "1331.20" xsd:float
-property_value: MassMono "1330.465790" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:137
-xref: GNO:G02815KT
-is_a: MOD:00725
-is_a: MOD:00160
-
-[Term]
-id: MOD:00507
-name: 5-dimethylaminonaphthalene-1-sulfonyl
-def: "OBSOLETE because redundant, replaced by MOD:01653. Remap to MOD:01653." [DeltaMass:0, Unimod:139]
-comment: From DeltaMass: Average Mass: 233
-synonym: "5-dimethylaminonaphthalene-1-sulfonyl" RELATED Unimod-description []
-synonym: "Dansyl" RELATED PSI-MS-label []
-synonym: "Dansyl (Dns)" EXACT DeltaMass-label []
-property_value: DiffAvg "233.29" xsd:float
-property_value: DiffFormula "C 12 H 11 N 1 O 2 S 1" xsd:string
-property_value: DiffMono "233.051050" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:139
-replaced_by: MOD:01653
-is_obsolete: true
-
-[Term]
-id: MOD:00508
-name: ISD a-series (C-Term)
-def: "OBSOLETE because this is an ion type and is not a biological or chemical modification to a polypeptide, can be handled by PSI-MS CV term, MS:1001229" [PubMed:14588022, Unimod:140]
-comment: Virtual Modification for MS/MS of a-type ions, by decarboxylation of C-terminus as reaction inside the mass spectrometer.
-synonym: "a-type-ion" RELATED PSI-MS-label []
-synonym: "ISD a-series (C-Term)" RELATED Unimod-description []
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: Unimod:140
-is_obsolete: true
-
-[Term]
-id: MOD:00509
-name: amidination of lysines or N-terminal amines with methyl acetimidate
-def: "modification from Unimod Chemical derivative" [PubMed:12643539, PubMed:6273432, Unimod:141]
-synonym: "amidination of lysines or N-terminal amines with methyl acetimidate" RELATED Unimod-description []
-synonym: "Amidine" RELATED PSI-MS-label []
-property_value: DiffAvg "41.05" xsd:float
-property_value: DiffFormula "C 2 H 3 N 1" xsd:string
-property_value: DiffMono "41.026549" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:141
-is_a: MOD:00848
-
-[Term]
-id: MOD:00510
-name: HexNAc1dHex1 N4-glycosylated asparagine
-def: "modification from Unimod N-linked glycosylation, dHex HexNAc" [OMSSA:183, PubMed:111247, PubMed:1694179, PubMed:5490222, RESID:AA0151#var, Unimod:142]
-synonym: "dHexHexNAcN" EXACT OMSSA-label []
-synonym: "HexNAc(1)dHex(1)" RELATED PSI-MS-label []
-synonym: "HexNAc1dHex1" RELATED Unimod-description []
-property_value: DiffAvg "349.34" xsd:float
-property_value: DiffFormula "C 14 H 23 N 1 O 9" xsd:string
-property_value: DiffMono "349.137281" xsd:float
-property_value: Formula "C 18 H 29 N 3 O 11" xsd:string
-property_value: MassAvg "463.44" xsd:float
-property_value: MassMono "463.180209" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:142
-xref: GNO:G00194GV
-is_a: MOD:00725
-is_a: MOD:00160
-
-[Term]
-id: MOD:00511
-name: HexNAc2 N4-glycosylated asparagine
-def: "modification from Unimod N-linked glycosylation, HexNAc(2)" [PubMed:111247, PubMed:1694179, PubMed:5490222, RESID:AA0151#var, Unimod:143]
-synonym: "HexNAc(2)" RELATED PSI-MS-label []
-synonym: "HexNAc2" RELATED Unimod-description []
-property_value: DiffAvg "406.39" xsd:float
-property_value: DiffFormula "C 16 H 26 N 2 O 10" xsd:string
-property_value: DiffMono "406.158745" xsd:float
-property_value: Formula "C 20 H 32 N 4 O 12" xsd:string
-property_value: MassAvg "520.49" xsd:float
-property_value: MassMono "520.201672" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:143
-xref: GNO:G27391WQ
-is_a: MOD:00725
-is_a: MOD:00160
-
-[Term]
-id: MOD:00512
-name: Hex3 N4-glycosylated asparagine
-def: "modification from Unimod N-linked glycosylation, Hex3" [PubMed:111247, PubMed:1694179, PubMed:5490222, RESID:AA0151#var, Unimod:144]
-synonym: "Hex(3)" RELATED PSI-MS-label []
-synonym: "Hex3" RELATED Unimod-description []
-property_value: DiffAvg "486.42" xsd:float
-property_value: DiffFormula "C 18 H 30 O 15" xsd:string
-property_value: DiffMono "486.158470" xsd:float
-property_value: Formula "C 22 H 36 N 2 O 17" xsd:string
-property_value: MassAvg "600.53" xsd:float
-property_value: MassMono "600.201398" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:144
-xref: GNO:G39365VM
-is_a: MOD:00725
-is_a: MOD:00160
-
-[Term]
-id: MOD:00513
-name: HexNAc1dHex2 N4-glycosylated asparagine
-def: "modification from Unimod N-linked glycosylation, dHex(2) HexNAc" [PubMed:111247, PubMed:1694179, PubMed:5490222, RESID:AA0151#var, Unimod:145]
-synonym: "HexNAc(1)dHex(2)" RELATED PSI-MS-label []
-synonym: "HexNAc1dHex2" RELATED Unimod-description []
-property_value: DiffAvg "495.48" xsd:float
-property_value: DiffFormula "C 20 H 33 N 1 O 13" xsd:string
-property_value: DiffMono "495.195190" xsd:float
-property_value: Formula "C 24 H 39 N 3 O 15" xsd:string
-property_value: MassAvg "609.58" xsd:float
-property_value: MassMono "609.238118" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:145
-xref: GNO:G74392IM
-is_a: MOD:00725
-is_a: MOD:00160
-
-[Term]
-id: MOD:00514
-name: Hex1HexNAc1dHex1 N4-glycosylated asparagine
-def: "modification from Unimod N-linked glycosylation, dHex Hex HexNAc" [PubMed:111247, PubMed:1694179, PubMed:5490222, RESID:AA0151#var, Unimod:146]
-synonym: "Hex(1)HexNAc(1)dHex(1)" RELATED PSI-MS-label []
-synonym: "Hex1HexNAc1dHex1" RELATED Unimod-description []
-property_value: DiffAvg "511.48" xsd:float
-property_value: DiffFormula "C 20 H 33 N 1 O 14" xsd:string
-property_value: DiffMono "511.190105" xsd:float
-property_value: Formula "C 24 H 39 N 3 O 16" xsd:string
-property_value: MassAvg "625.58" xsd:float
-property_value: MassMono "625.233032" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:146
-xref: GNO:G54129SE
-is_a: MOD:00725
-is_a: MOD:00160
-
-[Term]
-id: MOD:00515
-name: HexNAc2dHex1 N4-glycosylated asparagine
-def: "modification from Unimod N-linked glycosylation, dHex HexNAc(2)" [PubMed:111247, PubMed:1694179, PubMed:5490222, RESID:AA0151#var, Unimod:147]
-synonym: "HexNAc(2)dHex(1)" RELATED PSI-MS-label []
-synonym: "HexNAc2dHex1" RELATED Unimod-description []
-property_value: DiffAvg "552.53" xsd:float
-property_value: DiffFormula "C 22 H 36 N 2 O 14" xsd:string
-property_value: DiffMono "552.216654" xsd:float
-property_value: Formula "C 26 H 42 N 4 O 16" xsd:string
-property_value: MassAvg "666.63" xsd:float
-property_value: MassMono "666.259581" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:147
-xref: GNO:G06042JP
-is_a: MOD:00725
-is_a: MOD:00160
-
-[Term]
-id: MOD:00516
-name: Hex1HexNAc2 N4-glycosylated asparagine
-def: "modification from Unimod N-linked glycosylation" [RESID:AA0151#var, Unimod:148]
-synonym: "Hex(1)HexNAc(2)" RELATED PSI-MS-label []
-synonym: "Hex1HexNAc2" RELATED Unimod-description []
-property_value: DiffAvg "568.53" xsd:float
-property_value: DiffFormula "C 22 H 36 N 2 O 15" xsd:string
-property_value: DiffMono "568.211568" xsd:float
-property_value: Formula "C 26 H 42 N 4 O 17" xsd:string
-property_value: MassAvg "682.63" xsd:float
-property_value: MassMono "682.254496" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:148
-xref: GNO:G58001LT
-is_a: MOD:00725
-is_a: MOD:00160
-
-[Term]
-id: MOD:00517
-name: Hex1HexNAc1NeuAc1 glycosylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of an amino acid residue or of a modifying group with a carbohydrate-like group composed of Hex1HexNAc1NeuAc1 linked through a glycosidic bond." [DeltaMass:0, Unimod:149]
-comment: From DeltaMass: Average Mass: 657
-synonym: "Hex(1)HexNAc(1)NeuAc(1)" RELATED PSI-MS-label []
-synonym: "Hex1HexNAc1NeuAc1" RELATED Unimod-description []
-synonym: "NeuAc-Hex-HexNAc" EXACT DeltaMass-label []
-property_value: DiffAvg "657.60" xsd:float
-property_value: DiffFormula "C 25 H 41 N 2 O 18" xsd:string
-property_value: DiffMono "657.235437" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-xref: GNO:G17015OC
-is_a: MOD:00725
-
-[Term]
-id: MOD:00518
-name: HexNAc2dHex2 N4-glycosylated asparagine
-def: "modification from Unimod N-linked glycosylation" [RESID:AA0151#var, Unimod:150]
-synonym: "HexNAc(2)dHex(2)" RELATED PSI-MS-label []
-synonym: "HexNAc2dHex2" RELATED Unimod-description []
-property_value: DiffAvg "698.67" xsd:float
-property_value: DiffFormula "C 28 H 46 N 2 O 18" xsd:string
-property_value: DiffMono "698.274563" xsd:float
-property_value: Formula "C 32 H 52 N 4 O 20" xsd:string
-property_value: MassAvg "812.78" xsd:float
-property_value: MassMono "812.317490" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:150
-xref: GNO:G90423UY
-is_a: MOD:00725
-is_a: MOD:00160
-
-[Term]
-id: MOD:00519
-name: Hex1HexNAc2Pent1 N4-glycosylated asparagine
-def: "modification from Unimod N-linked glycosylation" [RESID:AA0151#var, Unimod:151]
-synonym: "Hex(1)HexNAc(2)Pent(1)" RELATED PSI-MS-label []
-synonym: "Hex1HexNAc2Pent1" RELATED Unimod-description []
-property_value: DiffAvg "700.64" xsd:float
-property_value: DiffFormula "C 27 H 44 N 2 O 19" xsd:string
-property_value: DiffMono "700.253827" xsd:float
-property_value: Formula "C 31 H 50 N 4 O 21" xsd:string
-property_value: MassAvg "814.75" xsd:float
-property_value: MassMono "814.296755" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:151
-xref: GNO:G54968WM
-is_a: MOD:00725
-is_a: MOD:00160
-
-[Term]
-id: MOD:00520
-name: Hex1HexNAc2dHex1 N4-glycosylated asparagine
-def: "modification from Unimod N-linked glycosylation" [RESID:AA0151#var, Unimod:152]
-synonym: "Hex(1)HexNAc(2)dHex(1)" RELATED PSI-MS-label []
-synonym: "Hex1HexNAc2dHex1" RELATED Unimod-description []
-property_value: DiffAvg "714.67" xsd:float
-property_value: DiffFormula "C 28 H 46 N 2 O 19" xsd:string
-property_value: DiffMono "714.269477" xsd:float
-property_value: Formula "C 32 H 52 N 4 O 21" xsd:string
-property_value: MassAvg "828.77" xsd:float
-property_value: MassMono "828.312405" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:152
-xref: GNO:G94583DZ
-is_a: MOD:00725
-is_a: MOD:00160
-
-[Term]
-id: MOD:00521
-name: Hex2HexNAc2 N4-glycosylated asparagine
-def: "modification from Unimod N-linked glycosylation" [RESID:AA0151#var, Unimod:153]
-synonym: "Hex(2)HexNAc(2)" RELATED PSI-MS-label []
-synonym: "Hex2HexNAc2" RELATED Unimod-description []
-property_value: DiffAvg "730.67" xsd:float
-property_value: DiffFormula "C 28 H 46 N 2 O 20" xsd:string
-property_value: DiffMono "730.264392" xsd:float
-property_value: Formula "C 32 H 52 N 4 O 22" xsd:string
-property_value: MassAvg "844.77" xsd:float
-property_value: MassMono "844.307319" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:153
-xref: GNO:G53434XO
-is_a: MOD:00725
-is_a: MOD:00160
-
-[Term]
-id: MOD:00522
-name: Hex3HexNAc1Pent1 N4-glycosylated asparagine
-def: "modification from Unimod N-linked glycosylation" [RESID:AA0151#var, Unimod:154]
-synonym: "Hex(3)HexNAc(1)Pent(1)" RELATED PSI-MS-label []
-synonym: "Hex3HexNAc1Pent1" RELATED Unimod-description []
-property_value: DiffAvg "821.73" xsd:float
-property_value: DiffFormula "C 31 H 51 N 1 O 24" xsd:string
-property_value: DiffMono "821.280102" xsd:float
-property_value: Formula "C 35 H 57 N 3 O 26" xsd:string
-property_value: MassAvg "935.84" xsd:float
-property_value: MassMono "935.323029" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:154
-xref: GNO:G64686LL
-is_a: MOD:00725
-is_a: MOD:00160
-
-[Term]
-id: MOD:00523
-name: Hex1HexNAc2dHex1Pent1 N4-glycosylated asparagine
-def: "modification from Unimod N-linked glycosylation" [RESID:AA0151#var, Unimod:155]
-synonym: "Hex(1)HexNAc(2)dHex(1)Pent(1)" RELATED PSI-MS-label []
-synonym: "Hex1HexNAc2dHex1Pent1" RELATED Unimod-description []
-property_value: DiffAvg "846.79" xsd:float
-property_value: DiffFormula "C 33 H 54 N 2 O 23" xsd:string
-property_value: DiffMono "846.311736" xsd:float
-property_value: Formula "C 35 H 57 N 3 O 26" xsd:string
-property_value: MassAvg "960.89" xsd:float
-property_value: MassMono "960.354663" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:155
-xref: GNO:G84825UQ
-is_a: MOD:00725
-is_a: MOD:00160
-
-[Term]
-id: MOD:00524
-name: Hex1HexNAc2dHex2 N4-glycosylated asparagine
-def: "modification from Unimod N-linked glycosylation" [RESID:AA0151#var, Unimod:156]
-synonym: "Hex(1)HexNAc(2)dHex(2)" RELATED PSI-MS-label []
-synonym: "Hex1HexNAc2dHex2" RELATED Unimod-description []
-property_value: DiffAvg "860.81" xsd:float
-property_value: DiffFormula "C 34 H 56 N 2 O 23" xsd:string
-property_value: DiffMono "860.327386" xsd:float
-property_value: Formula "C 38 H 62 N 4 O 25" xsd:string
-property_value: MassAvg "974.92" xsd:float
-property_value: MassMono "974.370313" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:156
-xref: GNO:G05460KC
-is_a: MOD:00725
-is_a: MOD:00160
-
-[Term]
-id: MOD:00525
-name: Hex2HexNAc2Pent1 N4-glycosylated asparagine
-def: "modification from Unimod N-linked glycosylation" [RESID:AA0151#var, Unimod:157]
-synonym: "Hex(2)HexNAc(2)Pent(1)" RELATED PSI-MS-label []
-synonym: "Hex2HexNAc2Pent1" RELATED Unimod-description []
-property_value: DiffAvg "862.79" xsd:float
-property_value: DiffFormula "C 33 H 54 N 2 O 24" xsd:string
-property_value: DiffMono "862.306651" xsd:float
-property_value: Formula "C 37 H 60 N 4 O 26" xsd:string
-property_value: MassAvg "976.89" xsd:float
-property_value: MassMono "976.349578" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:157
-xref: GNO:G18999EB
-is_a: MOD:00725
-is_a: MOD:00160
-
-[Term]
-id: MOD:00526
-name: Hex2HexNAc2dHex1 N4-glycosylated asparagine
-def: "modification from Unimod N-linked glycosylation" [RESID:AA0151#var, Unimod:158]
-synonym: "Hex(2)HexNAc(2)dHex(1)" RELATED PSI-MS-label []
-synonym: "Hex2HexNAc2dHex1" RELATED Unimod-description []
-property_value: DiffAvg "876.81" xsd:float
-property_value: DiffFormula "C 34 H 56 N 2 O 24" xsd:string
-property_value: DiffMono "876.322301" xsd:float
-property_value: Formula "C 38 H 62 N 4 O 26" xsd:string
-property_value: MassAvg "990.92" xsd:float
-property_value: MassMono "990.365228" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:158
-xref: GNO:G93579XB
-is_a: MOD:00725
-is_a: MOD:00160
-
-[Term]
-id: MOD:00527
-name: Hex3HexNAc2 N4-glycosylated asparagine
-def: "modification from Unimod N-linked glycosylation" [DeltaMass:0, RESID:AA0151#var, Unimod:159]
-comment: From DeltaMass: Average Mass: 893
-synonym: "(Hex)3-HexNAc-HexNAc" EXACT DeltaMass-label []
-synonym: "Hex(3)HexNAc(2)" RELATED PSI-MS-label []
-synonym: "Hex3HexNAc2" RELATED Unimod-description []
-property_value: DiffAvg "892.81" xsd:float
-property_value: DiffFormula "C 34 H 56 N 2 O 25" xsd:string
-property_value: DiffMono "892.317215" xsd:float
-property_value: Formula "C 38 H 62 N 4 O 27" xsd:string
-property_value: MassAvg "1006.92" xsd:float
-property_value: MassMono "1006.360143" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:159
-xref: GNO:G28681TP
-is_a: MOD:00725
-is_a: MOD:00160
-
-[Term]
-id: MOD:00528
-name: Hex1HexNAc1NeuAc2 glycosylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of an amino acid residue or of a modifying group with a carbohydrate-like group composed of Hex1HexNAc1NeuAc2 linked through a glycosidic bond." [Unimod:160]
-synonym: "Hex(1)HexNAc(1)NeuAc(2)" RELATED PSI-MS-label []
-synonym: "Hex1HexNAc1NeuAc2" RELATED Unimod-description []
-property_value: DiffAvg "947.85" xsd:float
-property_value: DiffFormula "C 36 H 57 N 3 O 26" xsd:string
-property_value: DiffMono "947.323029" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:160
-xref: GNO:G23729WG
-is_a: MOD:00725
-
-[Term]
-id: MOD:00529
-name: Hex3HexNAc2P1 N4-glycosylated asparagine
-def: "modification from Unimod N-linked glycosylation" [RESID:AA0151#var, Unimod:161]
-synonym: "Hex(3)HexNAc(2)P(1)" RELATED PSI-MS-label []
-synonym: "Hex3HexNAc2P1" RELATED Unimod-description []
-property_value: DiffAvg "972.79" xsd:float
-property_value: DiffFormula "C 34 H 57 N 2 O 28 P 1" xsd:string
-property_value: DiffMono "972.283546" xsd:float
-property_value: Formula "C 38 H 63 N 4 O 30 P 1" xsd:string
-property_value: MassAvg "1086.89" xsd:float
-property_value: MassMono "1086.326473" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:161
-xref: GNO:G88520YF
-is_a: MOD:00725
-is_a: MOD:00160
-
-[Term]
-id: MOD:00530
-name: L-selenomethionine
-def: "A protein modification that effectively converts an L-methionine residue to L-selenomethionine." [OMSSA:113, PubMed:12148805, Unimod:162#M]
-synonym: "Delta:S(-1)Se(1)" RELATED PSI-MS-label []
-synonym: "Se(S)Met" EXACT PSI-MOD-label []
-synonym: "Selenium replaces sulphur" RELATED Unimod-description []
-synonym: "semetm" EXACT OMSSA-label []
-property_value: DiffAvg "46.91" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 S -1 Se 1" xsd:string
-property_value: DiffMono "47.944450" xsd:float
-property_value: Formula "C 5 H 9 N 1 O 1 Se 1" xsd:string
-property_value: MassAvg "178.10" xsd:float
-property_value: MassMono "178.984935" xsd:float
-property_value: Origin "M" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:162
-is_a: MOD:00007
-is_a: MOD:00913
-
-[Term]
-id: MOD:00531
-name: (18)O labeled deglycosylated asparagine
-def: "A protein modification that effectively converts an L-asparagine residue to L-aspartic acid with one (18)O as the result of having been deglycosylated in (18)O water." [PubMed:14435542, Unimod:170]
-subset: PSI-MOD-slim
-synonym: "Delta:H(1)O(-1)18O(1)" RELATED PSI-MS-label []
-synonym: "glycosylated asparagine 18O labeling" RELATED Unimod-description []
-property_value: DiffAvg "2.99" xsd:float
-property_value: DiffFormula "H -1 N -1 (18)O 1" xsd:string
-property_value: DiffMono "2.988262" xsd:float
-property_value: Formula "C 4 H 5 N 1 (16)O 2 (18)O 1" xsd:string
-property_value: MassAvg "117.03" xsd:float
-property_value: MassMono "117.031189" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:170
-is_a: MOD:01293
-
-[Term]
-id: MOD:00532
-name: Shimadzu 13CNBS
-def: "modification from Unimod Chemical derivative" [PubMed:12845591, Unimod:171]
-synonym: "NBS:13C(6)" RELATED Unimod-interim []
-synonym: "Shimadzu NBS-13C" RELATED Unimod-description []
-property_value: DiffAvg "159.01" xsd:float
-property_value: DiffFormula "(13)C 6 H 3 N 1 O 2 S 1" xsd:string
-property_value: DiffMono "159.008578" xsd:float
-property_value: Formula "(12)C 11 (13)C 6 H 13 N 3 O 3 S 1" xsd:string
-property_value: MassAvg "345.09" xsd:float
-property_value: MassMono "345.087891" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:171
-is_a: MOD:01426
-
-[Term]
-id: MOD:00533
-name: Shimadzu 12CNBS
-def: "modification from Unimod Chemical derivative" [PubMed:12845591, Unimod:172]
-synonym: "NBS" RELATED Unimod-interim []
-synonym: "Shimadzu NBS-12C" RELATED Unimod-description []
-property_value: DiffAvg "152.99" xsd:float
-property_value: DiffFormula "(12)C 6 H 3 N 1 O 2 S 1" xsd:string
-property_value: DiffMono "152.988449" xsd:float
-property_value: Formula "(12)C 17 H 13 N 3 O 3 S 1" xsd:string
-property_value: MassAvg "339.07" xsd:float
-property_value: MassMono "339.067762" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:172
-is_a: MOD:01426
-
-[Term]
-id: MOD:00534
-name: Michael addition of BHT quinone methide to cysteine and lysine
-def: "modification from Unimod Post-translational" [PubMed:9448752, Unimod:176]
-comment: Butylated Hydroxytoluene adduct.
-synonym: "BHT" RELATED PSI-MS-label []
-synonym: "Michael addition of BHT quinone methide to Cysteine and Lysine" RELATED Unimod-description []
-property_value: DiffAvg "218.34" xsd:float
-property_value: DiffFormula "C 15 H 22 O 1" xsd:string
-property_value: DiffMono "218.167065" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:176
-is_a: MOD:00848
-
-[Term]
-id: MOD:00535
-name: phosphorylation to amine thiol
-def: "modification from Unimod Chemical derivative" [PubMed:12216740, Unimod:178]
-comment: DAET = 2-(dimethylamino)ethanethiol. The phosphorylation to amine is the beta elimination of phosphate and Michael addition of 2-(dimethylamino)ethanethiol to the site.
-synonym: "DAET" RELATED PSI-MS-label []
-synonym: "phosphorylation to amine thiol" RELATED Unimod-description []
-property_value: DiffAvg "87.18" xsd:float
-property_value: DiffFormula "C 4 H 9 N 1 O -1 S 1" xsd:string
-property_value: DiffMono "87.050656" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:178
-is_a: MOD:00848
-
-[Term]
-id: MOD:00536
-name: L-serine to L-alanine replacement
-def: "OBSOLETE because Unimod 179 merged with Unimod 447 remap to ??? a protein modification that replaces an L-serine residue with an L-alanine residue" [Unimod:179]
-synonym: "Ser_Ala" EXACT PSI-MOD-label []
-property_value: DiffAvg "-16.00" xsd:float
-property_value: DiffFormula "O -1" xsd:string
-property_value: DiffMono "-15.994915" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:179
-is_obsolete: true
-
-[Term]
-id: MOD:00537
-name: L-alanine residue (Thr)
-def: "A protein modification that effectively converts an L-threonine residue to L-alanine." [Unimod:659]
-comment: This could represent either an engineered replacement or a chemical modification.
-synonym: "Thr(Ala)" EXACT PSI-MOD-label []
-synonym: "Thr->Ala" RELATED Unimod-interim []
-synonym: "Thr->Ala substitution" RELATED Unimod-description []
-property_value: DiffAvg "-30.03" xsd:float
-property_value: DiffFormula "C -1 H -2 O -1" xsd:string
-property_value: DiffMono "-30.010565" xsd:float
-property_value: Formula "C 3 H 5 N 1 O 1" xsd:string
-property_value: MassAvg "71.08" xsd:float
-property_value: MassMono "71.037114" xsd:float
-property_value: Origin "T" xsd:string
-xref: Unimod:659
-is_a: MOD:00917
-
-[Term]
-id: MOD:00538
-name: protein modification categorized by isobaric sets
-def: "Modified amino acid residues groups into isobaric sets at particular mass resolution cut-offs." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:00000
-
-[Term]
-id: MOD:00539
-name: threonine reduced to aminobutynate
-def: "OBSOLETE because Unimod 179 merged wth Unimod 447 remap to ??? modification from Unimod O-linked glycosylation" [Unimod:182]
-property_value: DiffAvg "-17.01" xsd:float
-property_value: DiffFormula "H -1 O -1" xsd:string
-property_value: DiffMono "-17.002740" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:182
-is_obsolete: true
-
-[Term]
-id: MOD:00540
-name: 9x(13)C labeled residue
-def: "A protein modification that effectively converts a residue containing common isotopes to a 9x(13)C labeled residue." [PubMed:12716131, Unimod:184]
-synonym: "13C(9) Silac label" RELATED Unimod-description []
-synonym: "Label:13C(9)" RELATED PSI-MS-label []
-property_value: DiffAvg "9.03" xsd:float
-property_value: DiffFormula "(12)C -9 (13)C 9" xsd:string
-property_value: DiffMono "9.030194" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:184
-is_a: MOD:00842
-
-[Term]
-id: MOD:00541
-name: 9x(13)C labeled L-phosphotyrosine
-def: "A protein modification that effectively converts an L-tyrosine residue to 9x(13)C labeled L-phosphotyrosine." [PubMed:12716131, Unimod:185]
-synonym: "C13 label (Phosphotyrosine)" RELATED Unimod-description []
-synonym: "Label:13C(9)+Phospho" RELATED PSI-MS-label []
-property_value: DiffAvg "89.00" xsd:float
-property_value: DiffFormula "(12)C -9 (13)C 9 H 1 O 3 P 1" xsd:string
-property_value: DiffMono "88.996524" xsd:float
-property_value: Formula "(13)C 9 H 10 N 1 O 5 P 1" xsd:string
-property_value: MassAvg "252.06" xsd:float
-property_value: MassMono "252.059853" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:185
-is_a: MOD:00919
-is_a: MOD:00842
-relationship: derives_from MOD:00540
-relationship: derives_from MOD:00048
-
-[Term]
-id: MOD:00542
-name: hydroxyphenylglyoxal arginine
-def: "modification from Unimod Chemical derivative" [PubMed:11698400, PubMed:11914093, Unimod:186]
-synonym: "HPG" RELATED PSI-MS-label []
-synonym: "Hydroxyphenylglyoxal arginine" RELATED Unimod-description []
-property_value: DiffAvg "132.12" xsd:float
-property_value: DiffFormula "C 8 H 4 O 2" xsd:string
-property_value: DiffMono "132.021129" xsd:float
-property_value: Formula "C 14 H 16 N 4 O 3" xsd:string
-property_value: MassAvg "288.31" xsd:float
-property_value: MassMono "288.122240" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:186
-is_a: MOD:00902
-is_a: MOD:00848
-
-[Term]
-id: MOD:00543
-name: bis(hydroxyphenylglyoxal) arginine
-def: "modification from Unimod Chemical derivative" [PubMed:11698400, Unimod:187]
-comment: OH-PGO and PGO react with arginine at a stoichiometry of 2:1 [Unimod].
-synonym: "2HPG" RELATED PSI-MS-label []
-synonym: "bis(hydroxphenylglyoxal) arginine" RELATED Unimod-description []
-property_value: DiffAvg "282.25" xsd:float
-property_value: DiffFormula "C 16 H 10 O 5" xsd:string
-property_value: DiffMono "282.052823" xsd:float
-property_value: Formula "C 22 H 22 N 4 O 6" xsd:string
-property_value: MassAvg "438.44" xsd:float
-property_value: MassMono "438.153934" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:187
-is_a: MOD:00902
-is_a: MOD:00848
-
-[Term]
-id: MOD:00544
-name: 6x(13)C labeled residue
-def: "A protein modification that effectively converts a residue containing common isotopes to a 6x(13)C labeled residue." [PubMed:12716131, Unimod:188]
-subset: PSI-MOD-slim
-synonym: "13C(6) Silac label" RELATED Unimod-description []
-synonym: "Label:13C(6)" RELATED PSI-MS-label []
-property_value: DiffAvg "6.02" xsd:float
-property_value: DiffFormula "(12)C -6 (13)C 6" xsd:string
-property_value: DiffMono "6.020129" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:188
-is_a: MOD:00842
-
-[Term]
-id: MOD:00545
-name: deuterated dimethyl labeling (D)
-def: "OBSOLETE because redundant with MOD:00927. Remap to MOD:00927." [PubMed:14670044]
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-replaced_by: MOD:00927
-is_obsolete: true
-
-[Term]
-id: MOD:00546
-name: (18)O label at both C-terminal oxygens
-def: "A protein modification that effectively substitutes two (18)O atom for the two (16)O atoms of an alpha-carboxyl (1-carboxyl) group." [OMSSA:88, PubMed:11467524, Unimod:193]
-subset: PSI-MOD-slim
-synonym: "ctermpepdio18" EXACT OMSSA-label []
-synonym: "Label:18O(2)" RELATED PSI-MS-label []
-synonym: "O18 label at both C-terminal oxygens" RELATED Unimod-description []
-property_value: DiffAvg "4.01" xsd:float
-property_value: DiffFormula "(16)O -2 (18)O 2" xsd:string
-property_value: DiffMono "4.008493" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: Unimod:193
-is_a: MOD:00847
-
-[Term]
-id: MOD:00547
-name: 6-aminoquinolyl-N-hydroxysuccinimidyl carbamate
-def: "modification from Unimod Chemical derivative used for amino acid analysis" [PubMed:14997490, Unimod:194]
-synonym: "6-aminoquinolyl-N-hydroxysuccinimidyl carbamate" RELATED Unimod-description []
-synonym: "AccQTag" RELATED PSI-MS-label []
-property_value: DiffAvg "170.17" xsd:float
-property_value: DiffFormula "C 10 H 6 N 2 O 1" xsd:string
-property_value: DiffMono "170.048013" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:194
-is_a: MOD:00848
-
-[Term]
-id: MOD:00548
-name: APTA
-def: "modification from Unimod Chemical derivative" [PubMed:15283597, Unimod:195]
-comment: Derivatization of cysteine with 3-acrylamidopropyl)trimethylammonium chloride [JSG].
-synonym: "APTA-d0" RELATED Unimod-description []
-synonym: "QAT" RELATED PSI-MS-label []
-property_value: DiffAvg "171.26" xsd:float
-property_value: DiffFormula "C 9 H 19 N 2 O 1" xsd:string
-property_value: DiffMono "171.149738" xsd:float
-property_value: Formula "C 12 H 24 N 3 O 2 S 1" xsd:string
-property_value: MassAvg "274.40" xsd:float
-property_value: MassMono "274.158923" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:195
-is_a: MOD:00848
-
-[Term]
-id: MOD:00549
-name: APTA d3
-def: "modification from Unimod Isotopic label" [PubMed:15283597, Unimod:196]
-comment: Derivatization of cysteine with 3-acrylamidopropyl)trimethylammonium chloride (difference formula correct) [JSG].
-synonym: "(3-acrylamidopropyl)trimethylammonium" RELATED Unimod-description []
-synonym: "APTA d3" RELATED Unimod-description []
-synonym: "QAT:2H(3)" RELATED PSI-MS-label []
-property_value: DiffAvg "174.17" xsd:float
-property_value: DiffFormula "C 9 (1)H 16 (2)H 3 N 2 O 1" xsd:string
-property_value: DiffMono "174.168568" xsd:float
-property_value: Formula "C 12 (1)H 21 (2)H 3 N 3 O 2 S 1" xsd:string
-property_value: MassAvg "277.18" xsd:float
-property_value: MassMono "277.177753" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:196
-is_a: MOD:01431
-
-[Term]
-id: MOD:00550
-name: EAPTA d0
-def: "modification from Unimod Chemical derivative" [Unimod:197]
-synonym: "EAPTA d0" RELATED Unimod-description []
-synonym: "EQAT" RELATED PSI-MS-label []
-property_value: DiffAvg "184.28" xsd:float
-property_value: DiffFormula "C 10 H 20 N 2 O 1" xsd:string
-property_value: DiffMono "184.157563" xsd:float
-property_value: Formula "C 13 H 25 N 3 O 2 S 1" xsd:string
-property_value: MassAvg "287.42" xsd:float
-property_value: MassMono "287.166748" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:197
-is_a: MOD:01426
-
-[Term]
-id: MOD:00551
-name: EAPTA d5
-def: "modification from Unimod Isotopic label" [Unimod:198]
-synonym: "EAPTA d5" RELATED Unimod-description []
-synonym: "EQAT:2H(5)" RELATED PSI-MS-label []
-property_value: DiffAvg "189.19" xsd:float
-property_value: DiffFormula "C 10 (1)H 15 (2)H 5 N 2 O 1" xsd:string
-property_value: DiffMono "189.188947" xsd:float
-property_value: Formula "C 13 (1)H 20 (2)H 5 N 3 O 2 S 1" xsd:string
-property_value: MassAvg "292.20" xsd:float
-property_value: MassMono "292.198132" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:198
-is_a: MOD:01431
-
-[Term]
-id: MOD:00552
-name: 4x(2)H labeled dimethylated residue
-def: "A protein modification that effectively converts a residue containing common isotopes to a 4x(2)H labeled dimethylated residue." [PubMed:14670044, Unimod:199]
-comment: Supposed to be alpha-amino and Lys-N6 derivatized by C(2)H2O and reduction.
-subset: PSI-MOD-slim
-synonym: "DiMethyl-CHD2" RELATED Unimod-description []
-synonym: "Dimethyl:2H(4)" RELATED PSI-MS-label []
-property_value: DiffAvg "32.06" xsd:float
-property_value: DiffFormula "C 2 (2)H 4" xsd:string
-property_value: DiffMono "32.056407" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:199
-is_a: MOD:00839
-
-[Term]
-id: MOD:00553
-name: 1,2-ethanedithiol modified residue
-def: "A protein modification that effectively substitutes a (2-sulfanylethyl)sulfanyl (or thioethylthiol) group for a hydroxy group." [DeltaMass:0, PubMed:11507762, Unimod:200]
-comment: From DeltaMass: Average Mass: 93; supposed to be derivatization of serine and threonine.
-synonym: "1,2-ethanedithiol (EDT)" EXACT DeltaMass-label []
-synonym: "EDT" RELATED Unimod-description []
-synonym: "Ethanedithiol" RELATED PSI-MS-label []
-property_value: DiffAvg "76.18" xsd:float
-property_value: DiffFormula "C 2 H 4 O -1 S 2" xsd:string
-property_value: DiffMono "75.980528" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:200
-is_a: MOD:00848
-
-[Term]
-id: MOD:00554
-name: APTA-d0 with no neutral loss
-def: "OBSOLETE because Unimod entry 202 was merged with entry 195, remap to MOD:00548. modification from Unimod Chemical derivative" [Unimod:202]
-property_value: DiffAvg "170.26" xsd:float
-property_value: DiffFormula "C 9 H 18 N 2 O 1" xsd:string
-property_value: DiffMono "170.141913" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-replaced_by: MOD:00548
-xref: Unimod:202
-is_obsolete: true
-
-[Term]
-id: MOD:00555
-name: APTA-d0 with quaternary amine loss
-def: "OBSOLETE because Unimod entry 202 was merged with entry 195, remap to MOD:00548. modification from Unimod Chemical derivative" [Unimod:203]
-property_value: DiffAvg "170.26" xsd:float
-property_value: DiffFormula "C 9 H 18 N 2 O 1" xsd:string
-property_value: DiffMono "170.141913" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-replaced_by: MOD:00548
-xref: Unimod:203
-is_obsolete: true
-
-[Term]
-id: MOD:00556
-name: acrolein addition +94
-def: "OBSOLETE because this modification not supported by any literature that I can find[PMT]" [Unimod:205]
-synonym: "Acrolein addition +94" RELATED Unimod-description []
-synonym: "Delta:H(6)C(6)O(1)" RELATED PSI-MS-label []
-property_value: DiffAvg "94.11" xsd:float
-property_value: DiffFormula "C 6 H 6 O 1" xsd:string
-property_value: DiffMono "94.041865" xsd:float
-property_value: Formula "C 12 H 18 N 2 O 2" xsd:string
-property_value: MassAvg "222.29" xsd:float
-property_value: MassMono "222.136828" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:205
-is_obsolete: true
-
-[Term]
-id: MOD:00557
-name: acrolein addition +56
-def: "OBSOLETE because this modification not supported by the papers listed or any other that I can find[PMT]" [PubMed:10825247, PubMed:15541752, Unimod:206]
-synonym: "Acrolein addition +56" RELATED Unimod-description []
-synonym: "Delta:H(4)C(3)O(1)" RELATED PSI-MS-label []
-property_value: DiffAvg "56.06" xsd:float
-property_value: DiffFormula "C 3 H 4 O 1" xsd:string
-property_value: DiffMono "56.026215" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:206
-is_obsolete: true
-
-[Term]
-id: MOD:00558
-name: acrolein addition +38
-def: "OBSOLETE because this modification not supported by any literature that I can find[PMT]" [Unimod:207]
-synonym: "Acrolein addition +38" RELATED Unimod-description []
-synonym: "Delta:H(2)C(3)" RELATED PSI-MS-label []
-property_value: DiffAvg "38.05" xsd:float
-property_value: DiffFormula "C 3 H 2" xsd:string
-property_value: DiffMono "38.015650" xsd:float
-property_value: Formula "C 9 H 14 N 2 O 1" xsd:string
-property_value: MassAvg "166.22" xsd:float
-property_value: MassMono "166.110613" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:207
-is_obsolete: true
-
-[Term]
-id: MOD:00559
-name: acrolein addition +76
-def: "OBSOLETE because this modification not supported by any literature that I can find[PMT]" [Unimod:208]
-synonym: "Acrolein addition +76" RELATED Unimod-description []
-synonym: "Delta:H(4)C(6)" RELATED PSI-MS-label []
-property_value: DiffAvg "76.10" xsd:float
-property_value: DiffFormula "C 6 H 4" xsd:string
-property_value: DiffMono "76.031300" xsd:float
-property_value: Formula "C 12 H 16 N 2 O 1" xsd:string
-property_value: MassAvg "204.27" xsd:float
-property_value: MassMono "204.126263" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:208
-is_obsolete: true
-
-[Term]
-id: MOD:00560
-name: acrolein addition +112
-def: "OBSOLETE because this modification not supported by any literature that I can find[PMT]" [Unimod:209]
-synonym: "Acrolein addition +112" RELATED Unimod-description []
-synonym: "Delta:H(8)C(6)O(2)" RELATED PSI-MS-label []
-property_value: DiffAvg "112.13" xsd:float
-property_value: DiffFormula "C 6 H 8 O 2" xsd:string
-property_value: DiffMono "112.052429" xsd:float
-property_value: Formula "C 12 H 20 N 2 O 3" xsd:string
-property_value: MassAvg "240.30" xsd:float
-property_value: MassMono "240.147393" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:209
-is_obsolete: true
-
-[Term]
-id: MOD:00561
-name: N-ethyl iodoacetamide-
-def: "modification from Unimod Isotopic label" [PubMed:12766232, Unimod:211]
-synonym: "N-ethyl iodoacetamide-d0" RELATED Unimod-description []
-synonym: "NEIAA" RELATED PSI-MS-label []
-property_value: DiffAvg "85.11" xsd:float
-property_value: DiffFormula "C 4 H 7 N 1 O 1" xsd:string
-property_value: DiffMono "85.052764" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:211
-is_a: MOD:00848
-
-[Term]
-id: MOD:00562
-name: N-ethyl iodoacetamide-d5
-def: "modification from Unimod Isotopic label" [PubMed:12766232, Unimod:212]
-synonym: "N-ethyl iodoacetamide-d5" RELATED Unimod-description []
-synonym: "NEIAA:2H(5)" RELATED PSI-MS-label []
-property_value: DiffAvg "90.08" xsd:float
-property_value: DiffFormula "C 4 (1)H 2 (2)H 5 N 1 O 1" xsd:string
-property_value: DiffMono "90.084148" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:212
-is_a: MOD:01431
-
-[Term]
-id: MOD:00563
-name: mono-N-acetylaminogalactosylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with an N-acetylaminogalactose group through a glycosidic bond." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "GalNAcRes" EXACT PSI-MOD-label []
-synonym: "HexNAc" RELATED PSI-MS-label []
-property_value: DiffAvg "203.19" xsd:float
-property_value: DiffFormula "C 8 H 13 N 1 O 5" xsd:string
-property_value: DiffMono "203.079373" xsd:float
-property_value: Origin "X" xsd:string
-is_a: MOD:00734
-is_a: MOD:01673
-
-[Term]
-id: MOD:00564
-name: Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry
-def: "Modification from Unimod Isotopic label. The Unimod term was extracted when it had not been approved. OBSOLETE because redundant to MOD:01505. Remap to MOD:01505, or one of the child terms MOD:01493 or MOD:01497." [Unimod:214, URL:http\://docs.appliedbiosystems.com/pebiodocs/04351918.pdf]
-synonym: "iTRAQ4plex" RELATED Unimod-interim []
-synonym: "Representative mass and accurate mass for 116 & 117" RELATED Unimod-description []
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-replaced_by: MOD:01505
-xref: Unimod:214
-is_obsolete: true
-
-[Term]
-id: MOD:00565
-name: deglycosylated asparagine
-def: "modification from Unimod N-linked glycosylation" [Unimod:7#N]
-comment: Conversion of glycosylated asparagine residues upon deglycosylation with PGNase F in H2O. CAUTION - the difference formula appears to be based on a partial structure [JSG].
-synonym: "Deamidated" RELATED Unimod-interim []
-synonym: "Deamidation" RELATED Unimod-description []
-property_value: DiffAvg "0.98" xsd:float
-property_value: DiffFormula "H -1 N -1 O 1" xsd:string
-property_value: DiffMono "0.984016" xsd:float
-property_value: Formula "C 4 H 5 N 1 O 3" xsd:string
-property_value: MassAvg "115.09" xsd:float
-property_value: MassMono "115.026943" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:7
-is_a: MOD:00903
-
-[Term]
-id: MOD:00566
-name: label cysteine with IGBP reagent
-def: "modification from Unimod Chemical derivative" [Unimod:243]
-comment: \"IDBEST tag for quantitation, http://www.targetdiscovery.com/index.php?topic=prod.idbe\"
-synonym: "IGBP" RELATED PSI-MS-label []
-synonym: "Light IDBEST tag for quantitation" RELATED Unimod-description []
-property_value: DiffAvg "297.15" xsd:float
-property_value: DiffFormula "Br 1 C 12 H 13 N 2 O 2" xsd:string
-property_value: DiffMono "296.016040" xsd:float
-property_value: Formula "Br 1 C 15 H 18 N 3 O 3 S 1" xsd:string
-property_value: MassAvg "400.29" xsd:float
-property_value: MassMono "399.025225" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:243
-is_a: MOD:00905
-is_a: MOD:00848
-
-[Term]
-id: MOD:00567
-name: histidine oxidation to asparagine
-def: "OBSOLETE because Unimod entry 244 is redundant with Unimod 348. Remap to MOD:00775." [ChEBI:29956, PubMed:15736973, PubMed:5681232, PubMed:6692818, PubMed:9789001, RESID:AA0003, Unimod:244]
-property_value: DiffAvg "-23.04" xsd:float
-property_value: DiffFormula "C -2 H -1 N -1 O 1" xsd:string
-property_value: DiffMono "-23.015984" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:244
-is_obsolete: true
-
-[Term]
-id: MOD:00568
-name: histidine oxidation to aspartic acid
-def: "OBSOLETE because Unimod entry 245 is redundant with Unimod 349. Remap to MOD:00776" [PubMed:1097438, PubMed:339692, PubMed:4399050, PubMed:5764436, PubMed:6692818, PubMed:8089117, PubMed:9521123, PubMed:9582379, Unimod:245]
-property_value: DiffAvg "-22.05" xsd:float
-property_value: DiffFormula "C -2 H -2 N -2 O 2" xsd:string
-property_value: DiffMono "-22.031969" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-replaced_by: MOD:00776
-xref: Unimod:245
-is_obsolete: true
-
-[Term]
-id: MOD:00569
-name: residues isobaric at a resolution below 0.000001 Da
-def: "Natural or modified residues that are isobaric at a resolution below 0.000001 Da." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:00770
-
-[Term]
-id: MOD:00570
-name: residues isobaric at 71.037114 Da
-def: "Natural or modified residues with a mass of 71.037114 Da." [PubMed:18688235]
-is_a: MOD:00569
-is_a: MOD:00769
-
-[Term]
-id: MOD:00571
-name: 2-pyrrolidone-5-carboxylic acid (Pro)
-def: "A modification that effectively oxygenates C5 of an L-proline residue to form a 2-pyrrolidone-5-carboxylic acid, pyroglutamic acid." [OMSSA:111, PubMed:9252331, Unimod:359]
-comment: The review article PubMed:9252331 does not provide an original citation for this modification [JSG].
-synonym: "Pro->pyro-Glu" RELATED PSI-MS-label []
-synonym: "PyrGlu(Pro)" EXACT PSI-MOD-label []
-synonym: "Pyroglutamic" RELATED Unimod-interim []
-synonym: "pyroglutamicp" EXACT OMSSA-label []
-property_value: DiffAvg "13.98" xsd:float
-property_value: DiffFormula "H -2 O 1" xsd:string
-property_value: DiffMono "13.979265" xsd:float
-property_value: Formula "C 5 H 6 N 1 O 2" xsd:string
-property_value: MassAvg "112.11" xsd:float
-property_value: MassMono "112.039853" xsd:float
-property_value: Origin "P" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:359
-is_a: MOD:00679
-is_a: MOD:00915
-is_a: MOD:01048
-
-[Term]
-id: MOD:00572
-name: oxidized arginine biotinylated with biotin hydrazide
-def: "modification from Unimod Chemical derivative" [PubMed:15174056, PubMed:15828771, Unimod:343]
-synonym: "Argbiotinhydrazide" RELATED Unimod-interim []
-synonym: "oxidized Arginine biotinylated with biotin hydrazide" RELATED Unimod-description []
-property_value: DiffAvg "199.27" xsd:float
-property_value: DiffFormula "C 9 H 13 N 1 O 2 S 1" xsd:string
-property_value: DiffMono "199.066700" xsd:float
-property_value: Formula "C 15 H 25 N 5 O 3 S 1" xsd:string
-property_value: MassAvg "355.46" xsd:float
-property_value: MassMono "355.167811" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:343
-is_a: MOD:00848
-is_a: MOD:00902
-
-[Term]
-id: MOD:00573
-name: oxidized lysine biotinylated with biotin hydrazide
-def: "modification from Unimod Chemical derivative" [PubMed:15174056, Unimod:353]
-comment: \"http://www.piercenet.com/Proteomics/browse.cfm?fldID=84EBE112-F871-4CA5-807F-47327153CFCB\"
-synonym: "Lysbiotinhydrazide" RELATED Unimod-interim []
-synonym: "oxidized Lysine biotinylated with biotin hydrazide" RELATED Unimod-description []
-property_value: DiffAvg "241.31" xsd:float
-property_value: DiffFormula "C 10 H 15 N 3 O 2 S 1" xsd:string
-property_value: DiffMono "241.088498" xsd:float
-property_value: Formula "C 16 H 27 N 5 O 3 S 1" xsd:string
-property_value: MassAvg "369.48" xsd:float
-property_value: MassMono "369.183461" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:353
-is_a: MOD:00848
-is_a: MOD:00912
-
-[Term]
-id: MOD:00574
-name: oxidized proline biotinylated with biotin hydrazide
-def: "modification from Unimod Chemical derivative" [PubMed:15174056, Unimod:357]
-comment: \"http://www.piercenet.com/Proteomics/browse.cfm?fldID=84EBE112-F871-4CA5-807F-47327153CFCB\"
-synonym: "oxidized proline biotinylated with biotin hydrazide" RELATED Unimod-description []
-synonym: "probiotinhydrazide" RELATED Unimod-interim []
-property_value: DiffAvg "258.34" xsd:float
-property_value: DiffFormula "C 10 H 18 N 4 O 2 S 1" xsd:string
-property_value: DiffMono "258.115047" xsd:float
-property_value: Formula "C 15 H 25 N 5 O 3 S 1" xsd:string
-property_value: MassAvg "355.46" xsd:float
-property_value: MassMono "355.167811" xsd:float
-property_value: Origin "P" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:357
-is_a: MOD:00848
-is_a: MOD:00915
-
-[Term]
-id: MOD:00575
-name: oxidized threonine biotinylated with biotin hydrazide
-def: "modification from Unimod Chemical derivative" [PubMed:15174056, Unimod:361]
-comment: \"http://www.piercenet.com/Proteomics/browse.cfm?fldID=84EBE112-F871-4CA5-807F-47327153CFCB\"
-synonym: "oxidized Threonine biotinylated with biotin hydrazide" RELATED Unimod-description []
-synonym: "Thrbiotinhydrazide" RELATED Unimod-interim []
-property_value: DiffAvg "240.32" xsd:float
-property_value: DiffFormula "C 10 H 16 N 4 O 1 S 1" xsd:string
-property_value: DiffMono "240.104482" xsd:float
-property_value: Formula "C 14 H 23 N 5 O 3 S 1" xsd:string
-property_value: MassAvg "341.43" xsd:float
-property_value: MassMono "341.152161" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:361
-is_a: MOD:00848
-is_a: MOD:00917
-
-[Term]
-id: MOD:00576
-name: crotonylated residue
-def: "modification from Unimod Other" [PubMed:11283024, PubMed:25907603, Unimod:253]
-synonym: "Crotonaldehyde" RELATED PSI-MS-label []
-synonym: "Crotonaldehyde" RELATED Unimod-description []
-property_value: DiffAvg "70.09" xsd:float
-property_value: DiffFormula "C 4 H 6 O 1" xsd:string
-property_value: DiffMono "70.041865" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:253
-is_a: MOD:00649
-
-[Term]
-id: MOD:00577
-name: acetaldehyde crosslinked penta-L-lysine
-def: "modification occurs as a Schiff base in the presence of pentalysine" [PubMed:7744761, Unimod:254]
-synonym: "Acetaldehyde +26" RELATED Unimod-description []
-synonym: "Delta:H(2)C(2)" RELATED PSI-MS-label []
-property_value: DiffAvg "26.04" xsd:float
-property_value: DiffFormula "C 2 H 2" xsd:string
-property_value: DiffMono "26.015650" xsd:float
-property_value: Formula "C 8 H 14 N 2 O 1" xsd:string
-property_value: MassAvg "666.91" xsd:float
-property_value: MassMono "666.490465" xsd:float
-property_value: Origin "K, K, K, K, K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:254
-is_a: MOD:02051
-is_a: MOD:00692
-
-[Term]
-id: MOD:00578
-name: acetaldehyde +28
-def: "OBSOLETE because this modification not supported by any literature that I can find [PMT]" [Unimod:255]
-synonym: "Acetaldehyde +28" RELATED Unimod-description []
-synonym: "Delta:H(4)C(2)" RELATED PSI-MS-label []
-property_value: DiffAvg "28.05" xsd:float
-property_value: DiffFormula "C 2 H 4" xsd:string
-property_value: DiffMono "28.031300" xsd:float
-property_value: Formula "C " xsd:string
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:255
-is_obsolete: true
-
-[Term]
-id: MOD:00579
-name: propionaldehyde +40
-def: "OBSOLETE because not supported by the linked literature [PMT]. modification from Unimod Other" [Unimod:256]
-synonym: "Delta:H(4)C(3)" RELATED PSI-MS-label []
-synonym: "Propionaldehyde +40" RELATED Unimod-description []
-property_value: DiffAvg "40.06" xsd:float
-property_value: DiffFormula "C 3 H 4" xsd:string
-property_value: DiffMono "40.031300" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:256
-is_obsolete: true
-
-[Term]
-id: MOD:00580
-name: propionaldehyde +42
-def: "OBSOLETE because entry removed from Unimod. Remap potentially to MOD:00579 propionaldehyde +40" [Unimod:257]
-property_value: DiffAvg "42.08" xsd:float
-property_value: DiffFormula "C 3 H 6" xsd:string
-property_value: DiffMono "42.046950" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-replaced_by: MOD:00579
-xref: Unimod:257
-is_obsolete: true
-
-[Term]
-id: MOD:00581
-name: (18)O monosubstituted residue
-def: "A protein modification that effectively substitutes one (18)O atom for one (16)O atom." [OMSSA:87, PubMed:11467524, Unimod:258]
-subset: PSI-MOD-slim
-synonym: "ctermpepo18" EXACT OMSSA-label []
-synonym: "Label:18O(1)" RELATED PSI-MS-label []
-synonym: "O18 Labeling" RELATED Unimod-description []
-property_value: DiffAvg "2.00" xsd:float
-property_value: DiffFormula "(16)O -1 (18)O 1" xsd:string
-property_value: DiffMono "2.004246" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: Unimod:258
-is_a: MOD:00845
-
-[Term]
-id: MOD:00582
-name: 6x(13)C,2x(15)N labeled L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to 6x(13)C,2x(15)N labeled L-lysine." [OMSSA:181, PubMed:12716131, Unimod:259]
-synonym: "13C(6) 15N(2) Silac label" RELATED Unimod-description []
-synonym: "Label:13C(6)15N(2)" RELATED PSI-MS-label []
-synonym: "lys-13C615N2" EXACT OMSSA-label []
-property_value: DiffAvg "8.01" xsd:float
-property_value: DiffFormula "(12)C -6 (13)C 6 (14)N -2 (15)N 2" xsd:string
-property_value: DiffMono "8.014199" xsd:float
-property_value: Formula "(13)C 6 H 12 (15)N 2 O 1" xsd:string
-property_value: MassAvg "136.11" xsd:float
-property_value: MassMono "136.109162" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:259
-is_a: MOD:00842
-is_a: MOD:00843
-is_a: MOD:00912
-
-[Term]
-id: MOD:00583
-name: thiophosphorylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with a thiophosphono group (H2PO2S, 'thiophosphate')." [PubMed:12110917, Unimod:260]
-synonym: "Thiophospho" RELATED PSI-MS-label []
-synonym: "Thiophosphorylation" RELATED Unimod-description []
-property_value: DiffAvg "96.04" xsd:float
-property_value: DiffFormula "H 1 O 2 P 1 S 1" xsd:string
-property_value: DiffMono "95.943487" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:260
-is_a: MOD:00860
-is_a: MOD:00861
-
-[Term]
-id: MOD:00584
-name: 4-sulfophenyl isothiocyanate derivatized residue
-def: "A protein modification produced by formation of an adduct with 4-sulfophenyl isothiocyanate." [PubMed:14689565, PubMed:14745769, PubMed:16526082, Unimod:261]
-synonym: "4-sulfophenyl isothiocyanate" RELATED Unimod-description []
-synonym: "SPITC" RELATED PSI-MS-label []
-property_value: DiffAvg "215.24" xsd:float
-property_value: DiffFormula "C 7 H 5 N 1 O 3 S 2" xsd:string
-property_value: DiffMono "214.971085" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:261
-is_a: MOD:00841
-
-[Term]
-id: MOD:00585
-name: deuterium trisubstituted residue
-def: "A protein modification that effectively substitutes three (2)H deuterium atoms for three (1)H protium atoms." [Unimod:262]
-synonym: "D(H)3Res" EXACT PSI-MOD-label []
-synonym: "Label:2H(3)" RELATED PSI-MS-label []
-synonym: "Trideuteration" RELATED Unimod-description []
-property_value: DiffAvg "3.02" xsd:float
-property_value: DiffFormula "(1)H -3 (2)H 3" xsd:string
-property_value: DiffMono "3.018830" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:262
-is_a: MOD:00786
-
-[Term]
-id: MOD:00586
-name: pyridyl thiol modified residue
-def: "modification from Unimod Chemical derivative" [Unimod:264]
-synonym: "PET" RELATED PSI-MS-label []
-synonym: "phosphorylation to pyridyl thiol" RELATED Unimod-description []
-property_value: DiffAvg "121.20" xsd:float
-property_value: DiffFormula "C 7 H 7 N 1 O -1 S 1" xsd:string
-property_value: DiffMono "121.035006" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:264
-is_a: MOD:00848
-
-[Term]
-id: MOD:00587
-name: 6x(13)C,4x(15)N labeled L-arginine
-def: "A protein modification that effectively converts an L-arginine residue to 6x(13)C, 4x(15)N labeled L-arginine." [OMSSA:137, PubMed:12716131, Unimod:267]
-subset: PSI-MOD-slim
-synonym: "13C(6) 15N(4) Silac label" RELATED Unimod-description []
-synonym: "arg-13c6-15n4" EXACT OMSSA-label []
-synonym: "Label:13C(6)15N(4)" RELATED PSI-MS-label []
-property_value: DiffAvg "10.01" xsd:float
-property_value: DiffFormula "(12)C -6 (13)C 6 (14)N -4 (15)N 4" xsd:string
-property_value: DiffMono "10.008269" xsd:float
-property_value: Formula "(13)C 6 H 12 (15)N 4 O 1" xsd:string
-property_value: MassAvg "166.11" xsd:float
-property_value: MassMono "166.109380" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:267
-is_a: MOD:00842
-is_a: MOD:00843
-is_a: MOD:00902
-
-[Term]
-id: MOD:00588
-name: 5x(13)C,1x(15)N labeled L-valine
-def: "A protein modification that effectively converts an L-valine residue to 5x(13)C,1x(15)N labeled L-valine." [PubMed:12771378, Unimod:268#V]
-synonym: "13C(5) 15N(1) Silac label" RELATED Unimod-description []
-synonym: "Label:13C(5)15N(1)" RELATED PSI-MS-label []
-property_value: DiffAvg "6.01" xsd:float
-property_value: DiffFormula "(12)C -5 (13)C 5 (14)N -1 (15)N 1" xsd:string
-property_value: DiffMono "6.013809" xsd:float
-property_value: Formula "(13)C 5 H 9 (15)N 1 O 1" xsd:string
-property_value: MassAvg "105.08" xsd:float
-property_value: MassMono "105.082223" xsd:float
-property_value: Origin "V" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:268
-is_a: MOD:00920
-is_a: MOD:01809
-
-[Term]
-id: MOD:00589
-name: 9x(13)C,1x(15)N labeled L-phenylalanine
-def: "A protein modification that effectively converts an L-phenylalanine residue to (13)C,(15)N labeled L-phenylalanine." [PubMed:12771378, Unimod:269]
-synonym: "13C(9) 15N(1) Silac label" RELATED Unimod-description []
-synonym: "Label:13C(9)15N(1)" RELATED PSI-MS-label []
-property_value: DiffAvg "10.03" xsd:float
-property_value: DiffFormula "(12)C -9 (13)C 9 (14)N -1 (15)N 1" xsd:string
-property_value: DiffMono "10.027228" xsd:float
-property_value: Formula "(13)C 9 H 9 (15)N 1 O 1" xsd:string
-property_value: MassAvg "157.10" xsd:float
-property_value: MassMono "157.095642" xsd:float
-property_value: Origin "F" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:269
-is_a: MOD:00842
-is_a: MOD:00843
-is_a: MOD:00914
-
-[Term]
-id: MOD:00590
-name: nucleophilic addtion to cytopiloyne
-def: "OBSOLETE because there is no evidence in the literature of covalent modification of polypeptides with cytopiloyne or cytopiloyne+H2O.  Modifications could potentially happen, but are not experimentally verified. [PMT] modification from Unimod Chemical derivative" [PubMed:15549660, Unimod:270]
-synonym: "Cytopiloyne" RELATED PSI-MS-label []
-synonym: "nucleophilic addtion to cytopiloyne" RELATED Unimod-description []
-property_value: DiffAvg "362.38" xsd:float
-property_value: DiffFormula "C 19 H 22 O 7" xsd:string
-property_value: DiffMono "362.136553" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:270
-is_obsolete: true
-
-[Term]
-id: MOD:00591
-name: nucleophilic addition to cytopiloyne+H2O
-def: "OBSOLETE because there is no evidence in the literature of covalent modification of polypeptides with cytopiloyne or cytopiloyne+H2O.  Modifications could potentially happen, but are not experimentally verified. [PMT] modification from Unimod Chemical derivative" [PubMed:15549660, Unimod:271]
-synonym: "Cytopiloyne+water" RELATED PSI-MS-label []
-synonym: "nucleophilic addition to cytopiloyne+H2O" RELATED Unimod-description []
-property_value: DiffAvg "380.39" xsd:float
-property_value: DiffFormula "C 19 H 24 O 8" xsd:string
-property_value: DiffMono "380.147118" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:271
-is_obsolete: true
-
-[Term]
-id: MOD:00592
-name: sulfonation of N-terminal
-def: "modification from Unimod Chemical derivative" [PubMed:12705581, PubMed:15732931, PubMed:16046801, Unimod:272]
-synonym: "CAF" RELATED PSI-MS-label []
-synonym: "sulfonation of N-terminus" RELATED Unimod-description []
-property_value: DiffAvg "136.12" xsd:float
-property_value: DiffFormula "C 3 H 4 O 4 S 1" xsd:string
-property_value: DiffMono "135.983030" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:272
-is_a: MOD:00848
-
-[Term]
-id: MOD:00593
-name: covalent modification of lysine by omega-maleimido alkanoyl N-hydroxysuccinimido esters
-def: "OBSOLETE because removed from Unimod. modification from Unimod Chemical derivative" [Unimod:273]
-comment: J. Prot. Chem. 2, 263-277, 1983
-synonym: "covalent modification of lysine by cross-linking reagent" RELATED Unimod-description []
-synonym: "Xlink:SSD" RELATED PSI-MS-label []
-property_value: DiffAvg "253.25" xsd:float
-property_value: DiffFormula "C 12 H 15 N 1 O 5" xsd:string
-property_value: DiffMono "253.095023" xsd:float
-property_value: Formula "C 18 H 27 N 3 O 6" xsd:string
-property_value: MassAvg "381.43" xsd:float
-property_value: MassMono "381.189986" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:273
-is_obsolete: true
-
-[Term]
-id: MOD:00594
-name: residues isobaric at 113.047678 Da
-def: "Natural or modified resiues with a mass of 113.047678 Da." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:00569
-is_a: MOD:00624
-
-[Term]
-id: MOD:00595
-name: monomannosylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with an manose group through a glycosidic bond" [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "ManRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "162.14" xsd:float
-property_value: DiffFormula "C 6 H 10 O 5" xsd:string
-property_value: DiffMono "162.052823" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00727
-is_a: MOD:00761
-
-[Term]
-id: MOD:00596
-name: 4-(2-aminoethyl)benzenesulfonyl fluoride derivatized residue
-def: "A protein modification that is produced by formation of an adduct with 4-(2-aminoethyl)benzenesulfonyl fluoride, AEBS." [DeltaMass:235, PubMed:8597590, Unimod:276]
-comment: From DeltaMass: Average Mass: 183 Average Mass Change:183 References:We have found that AEBSF modifies many proteins by covalent attachment, preferentially on Tyr, and to a lesser extent on Lys, His, and the amino-terminus. These modifications were identified by electrospray MS of the proteins (adds 183 Da per AEBS-group) and by peptide mapping and MS/MS. All the proteins we examined were modified after 24 hrs. at 4 C with 1 mM AEBSF in TRIS, pH 8.0. The reaction is 10-20x slower at pH 7; however AEBSF is quite stable in aqueous solution and the extent of to which the protein is modified continues to increase for several days. We have seen the addition of 10 or more AEBS-groups to proteins after prolonged storage. We found no equivalent modification from PMSF, probably because it degrades so quickly. We no longer use AEBSF, and urge caution to those who do. To address the problem, Boehringer Mannheim (now Roche Molecular Biochemicals) introduced Pefabloc PLUS which includes an additional component to compete for these side reactions. In our limited experience with Pefabloc PLUS, it reduces the +183 modifications, but does not always eliminate them. As a result, we prefer PMSF, despite its own set of drawbacks. We have never found PMSF-induced modification of proteins (except trypsin), probably due to its short half-life in aqeous solution.
-synonym: "AEBS" RELATED PSI-MS-label []
-synonym: "AEBSF" EXACT DeltaMass-label []
-synonym: "Aminoethylbenzenesulfonylation" RELATED Unimod-description []
-property_value: DiffAvg "183.23" xsd:float
-property_value: DiffFormula "C 8 H 9 N 1 O 2 S 1" xsd:string
-property_value: DiffMono "183.035400" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:276
-is_a: MOD:01652
-
-[Term]
-id: MOD:00597
-name: methyl methanethiosulfonate
-def: "OBSOLETE because Unimod entry 277 redundant with Unimod 39. Remap to MOD:00110." [Unimod:277]
-property_value: DiffAvg "46.09" xsd:float
-property_value: DiffFormula "C 1 H 2 S 1" xsd:string
-property_value: DiffMono "45.987721" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-replaced_by: MOD:00110
-xref: Unimod:277
-is_obsolete: true
-
-[Term]
-id: MOD:00598
-name: S-(2-hydroxyethyl)cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-(2-hydroxyethyl)cysteine" [PubMed:15351294, Unimod:278]
-comment: This modification of cysteine is produced by the reagent iodoethanol with triethylphosphine [JSG].
-subset: PSI-MOD-slim
-synonym: "Ethanolation of Cys" RELATED Unimod-description []
-synonym: "Ethanolyl" RELATED PSI-MS-label []
-property_value: DiffAvg "44.05" xsd:float
-property_value: DiffFormula "C 2 H 4 O 1" xsd:string
-property_value: DiffMono "44.026215" xsd:float
-property_value: Formula "C 5 H 9 N 1 O 2 S 1" xsd:string
-property_value: MassAvg "147.19" xsd:float
-property_value: MassMono "147.035400" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:278
-is_a: MOD:00905
-
-[Term]
-id: MOD:00599
-name: monomethylated residue
-def: "A protein modification that effectively replaces one hydrogen atom with one methyl group." [PubMed:11875433, Unimod:34]
-subset: PSI-MOD-slim
-synonym: "Me1Res" EXACT PSI-MOD-label []
-synonym: "Methyl" RELATED PSI-MS-label []
-synonym: "Methylation" RELATED Unimod-description []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Origin "X" xsd:string
-xref: Unimod:34
-is_a: MOD:00427
-
-[Term]
-id: MOD:00600
-name: L-glutamic acid 5-ethyl ester
-def: "A protein modification that effectively converts an L-glutamic acid residue to L-glutamate 5-ethyl ester." [DeltaMass:0, PubMed:9629898, Unimod:280#E]
-comment: From DeltaMass: Average Mass: 28 with no citation. The Unimod citation refers to the formation of glutamate ethyl ester and not to either lysine or N-terminal alkylation. For dimethylated residues, see MOD:00429 and its children [JSG].
-synonym: "Ethyl" EXACT DeltaMass-label []
-synonym: "Ethyl" RELATED PSI-MS-label []
-synonym: "Ethylation" RELATED Unimod-description []
-property_value: DiffAvg "28.05" xsd:float
-property_value: DiffFormula "C 2 H 4" xsd:string
-property_value: DiffMono "28.031300" xsd:float
-property_value: Formula "C 7 H 11 N 1 O 3" xsd:string
-property_value: MassAvg "157.17" xsd:float
-property_value: MassMono "157.073893" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:280
-is_a: MOD:00906
-is_a: MOD:01339
-
-[Term]
-id: MOD:00601
-name: cyclized residue
-def: "A protein modification that effectively produces an heterocyclic amino acid with a covalent bond between the side chain and either its alpha amino or 1-carboxyl group, possibly breaking the peptide chain." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "CycRes" EXACT PSI-MOD-label []
-is_a: MOD:01156
-
-[Term]
-id: MOD:00602
-name: N-methylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of a residue amino or imino group with an methyl group." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "NMeRes" EXACT PSI-MOD-label []
-is_a: MOD:00427
-
-[Term]
-id: MOD:00603
-name: N-ethylation
-def: "OBSOLETE because Unimod entry 283 is redundant with Unimod 280. Remap to MOD:00600" [Unimod:283]
-property_value: DiffAvg "28.05" xsd:float
-property_value: DiffFormula "C 2 H 4" xsd:string
-property_value: DiffMono "28.031300" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-replaced_by: MOD:00600
-xref: Unimod:283
-is_obsolete: true
-
-[Term]
-id: MOD:00604
-name: 2x(2)H monomethylated L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to 2x(2)H labeled monomethylated L-lysine." [PubMed:15525938, Unimod:284]
-synonym: "Deuterium Methylation of Lysine" RELATED Unimod-description []
-synonym: "Methyl:2H(2)" RELATED PSI-MS-label []
-property_value: DiffAvg "16.03" xsd:float
-property_value: DiffFormula "C 1 (2)H 2" xsd:string
-property_value: DiffMono "16.028204" xsd:float
-property_value: Formula "C 7 (1)H 12 (2)H 2 N 2 O 1" xsd:string
-property_value: MassAvg "144.12" xsd:float
-property_value: MassMono "144.123167" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:284
-is_a: MOD:00839
-is_a: MOD:00912
-relationship: derives_from MOD:00085
-
-[Term]
-id: MOD:00605
-name: Sulfanilic Acid (SA), light C12
-def: "modification from Unimod Chemical derivative, C-Terminal/Glutamate/Aspartate sulfonation" [Unimod:285]
-synonym: "Light Sulfanilic Acid (SA) C12" RELATED Unimod-description []
-synonym: "SulfanilicAcid" RELATED PSI-MS-label []
-property_value: DiffAvg "155.00" xsd:float
-property_value: DiffFormula "(12)C 6 H 5 N 1 O 2 S 1" xsd:string
-property_value: DiffMono "155.004099" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: Unimod:285
-is_a: MOD:01426
-
-[Term]
-id: MOD:00606
-name: Sulfanilic Acid (SA), heavy C13
-def: "modification from Unimod Chemical derivative" [PubMed:9254591, Unimod:286]
-synonym: "Heavy Sulfanilic Acid (SA) C13" RELATED Unimod-description []
-synonym: "SulfanilicAcid:13C(6)" RELATED PSI-MS-label []
-property_value: DiffAvg "161.02" xsd:float
-property_value: DiffFormula "(13)C 6 H 5 N 1 O 2 S 1" xsd:string
-property_value: DiffMono "161.024228" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: Unimod:286
-is_a: MOD:01428
-
-[Term]
-id: MOD:00607
-name: dioxoindolealanine lactone
-def: "modification from Unimod Chemical derivative" [PubMed:7949339, Unimod:288]
-comment: Unimod name, formula, and terminal specification corrected. Formula corresponded to uncleaved intermediate [JSG].
-synonym: "Trp->Oxolactone" RELATED PSI-MS-label []
-synonym: "Tryptophan oxidation to oxolactone" RELATED Unimod-description []
-property_value: DiffAvg "30.99" xsd:float
-property_value: DiffFormula "H -1 O 2" xsd:string
-property_value: DiffMono "30.982004" xsd:float
-property_value: Formula "C 11 H 9 N 2 O 3" xsd:string
-property_value: MassAvg "217.20" xsd:float
-property_value: MassMono "217.061317" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: Unimod:288
-is_a: MOD:00918
-
-[Term]
-id: MOD:00608
-name: biotin polyethyleneoxide amine
-def: "modification from Unimod Chemical derivative" [Unimod:289]
-synonym: "Biotin polyethyleneoxide amine" RELATED Unimod-description []
-synonym: "Biotin-PEO-Amine" RELATED Unimod-interim []
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:289
-is_a: MOD:00848
-
-[Term]
-id: MOD:00609
-name: Pierce EZ-Link Biotin-HPDP modified L-cysteine
-def: "modification from Unimod Chemical derivative" [Unimod:290]
-synonym: "Biotin-HPDP" RELATED Unimod-interim []
-synonym: "Pierce EZ-Link Biotin-HPDP" RELATED Unimod-description []
-property_value: DiffAvg "428.61" xsd:float
-property_value: DiffFormula "C 19 H 32 N 4 O 3 S 2" xsd:string
-property_value: DiffMono "428.191583" xsd:float
-property_value: Formula "C 22 H 37 N 5 O 4 S 3" xsd:string
-property_value: MassAvg "531.75" xsd:float
-property_value: MassMono "531.200768" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:290
-is_a: MOD:00905
-is_a: MOD:00848
-
-[Term]
-id: MOD:00610
-name: cysteinyl mercury
-def: "modification from Unimod Chemical derivative" [PubMed:10695144, Unimod:291]
-synonym: "Delta:Hg(1)" RELATED PSI-MS-label []
-synonym: "Mercury Mercaptan" RELATED Unimod-description []
-property_value: DiffAvg "200.59" xsd:float
-property_value: DiffFormula "Hg 1" xsd:string
-property_value: DiffMono "201.970643" xsd:float
-property_value: Formula "C 3 H 5 Hg 1 N 1 O 1 S 1" xsd:string
-property_value: MassAvg "303.73" xsd:float
-property_value: MassMono "304.979828" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:291
-is_a: MOD:00848
-is_a: MOD:02067
-is_a: MOD:01075
-
-[Term]
-id: MOD:00611
-name: iodouridine monophosphate derivatized residue
-def: "A protein modification that is produced by reaction of iodouridine monophosphate with a residue." [PubMed:11112526, PubMed:11567090, PubMed:6540775, Unimod:292]
-synonym: "Cross-link of (Iodo)-uracil MP with W,F,Y" RELATED Unimod-description []
-synonym: "IodoU-AMP" RELATED PSI-MS-label []
-property_value: DiffAvg "322.17" xsd:float
-property_value: DiffFormula "C 9 H 11 N 2 O 9 P 1" xsd:string
-property_value: DiffMono "322.020217" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:292
-is_a: MOD:00848
-
-[Term]
-id: MOD:00612
-name: 3-(carboxamidomethylthio)propanoylated residue
-def: "A protein modification that is produced by derivatization of a residue with 3,3-dithiobis[sulfosuccinimidyl propanoate], DTSSP, or with Pierce EZ-Link Sulfo-NHS-SS-Biotin reagent, sulfosuccinimidyl 3-[(2-[biotinamido]ethyl)disulfanyl]propanoate, followed by reduction with dithiothreitol and then reaction with iodoacetamide." [PubMed:15121203, Unimod:293]
-synonym: "3-(carbamidomethylthio)propanoyl" RELATED Unimod-description []
-synonym: "CAMthiopropanoyl" RELATED PSI-MS-label []
-property_value: DiffAvg "145.18" xsd:float
-property_value: DiffFormula "C 5 H 7 N 1 O 2 S 1" xsd:string
-property_value: DiffMono "145.019749" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:293
-is_a: MOD:00649
-is_a: MOD:00848
-
-[Term]
-id: MOD:00613
-name: biotinoyl-iodoacetyl-ethylenediamine
-def: "modification from Unimod Chemical derivative" [PubMed:10906242, Unimod:294]
-synonym: "biotinoyl-iodoacetyl-ethylenediamine" RELATED Unimod-description []
-synonym: "IED-Biotin" RELATED PSI-MS-label []
-property_value: DiffAvg "326.42" xsd:float
-property_value: DiffFormula "C 14 H 22 N 4 O 3 S 1" xsd:string
-property_value: DiffMono "326.141262" xsd:float
-property_value: Formula "C 17 H 27 N 5 O 4 S 2" xsd:string
-property_value: MassAvg "429.55" xsd:float
-property_value: MassMono "429.150446" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:294
-is_a: MOD:00848
-is_a: MOD:00905
-
-[Term]
-id: MOD:00614
-name: fucosylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of an amino acid residue or of a modifying group with a fucose (6-deoxy-D-galactose) group through a glycosidic bond." [PubMed:11344537, PubMed:15189151, Unimod:295]
-subset: PSI-MOD-slim
-synonym: "dHex" RELATED PSI-MS-label []
-synonym: "Fuc" EXACT PSI-MOD-label []
-synonym: "Fucose" RELATED Unimod-description []
-property_value: DiffAvg "146.14" xsd:float
-property_value: DiffFormula "C 6 H 10 O 4" xsd:string
-property_value: DiffMono "146.057909" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:295
-xref: GNO:G49112ZN
-is_a: MOD:00736
-
-[Term]
-id: MOD:00615
-name: 4-sulfophenyl isothiocyante modification to N-term R
-def: "OBSOLETE because entry Unimod:261 site N-term R was abandoned. Remap to MOD:00584" [PubMed:14689565, Unimod:261]
-property_value: DiffAvg "215.24" xsd:float
-property_value: DiffFormula "C 7 H 5 N 1 O 3 S 2" xsd:string
-property_value: DiffMono "214.971085" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-replaced_by: MOD:00584
-xref: Unimod:261
-is_obsolete: true
-
-[Term]
-id: MOD:00616
-name: residues isobaric at a resolution below 0.1 Da
-def: "Natural or modified residues that are isobaric at a resolution below 0.1 Da." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:00538
-
-[Term]
-id: MOD:00617
-name: 3x(2)H residue methyl ester
-def: "A protein modification that effectively converts a residue containing common isotopes to a 3x(2)H labeled residue methyl ester." [OMSSA:21, Unimod:298]
-synonym: "ctermpeptrideuteromethyl" EXACT OMSSA-label []
-synonym: "deuterated methyl ester" RELATED Unimod-description []
-synonym: "Methyl:2H(3)" RELATED PSI-MS-label []
-property_value: DiffAvg "17.03" xsd:float
-property_value: DiffFormula "C 1 (1)H -1 (2)H 3" xsd:string
-property_value: DiffMono "17.034480" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: Unimod:298
-is_a: MOD:00839
-
-[Term]
-id: MOD:00618
-name: tryptophan carboxylation
-def: "modification from Unimod Chemical derivative" [Unimod:299#W]
-comment: There is no literature citation for this Unimod entry [JSG].
-synonym: "Carboxy" RELATED Unimod-interim []
-synonym: "Carboxylation" RELATED Unimod-description []
-property_value: DiffAvg "44.01" xsd:float
-property_value: DiffFormula "C 1 O 2" xsd:string
-property_value: DiffMono "43.989829" xsd:float
-property_value: Formula "C 12 H 10 N 2 O 3" xsd:string
-property_value: MassAvg "230.22" xsd:float
-property_value: MassMono "230.069142" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:299
-is_a: MOD:00918
-is_a: MOD:01152
-
-[Term]
-id: MOD:00619
-name: hydroxylethanone
-def: "OBSOLETE because entry 300 is redundant with Unimod 6 remap to MOD:01328" [Unimod:300]
-property_value: DiffAvg "58.04" xsd:float
-property_value: DiffFormula "C 2 H 2 O 2" xsd:string
-property_value: DiffMono "58.005479" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "artifact" xsd:string
-replaced_by: MOD:01328
-xref: Unimod:300
-is_obsolete: true
-
-[Term]
-id: MOD:00620
-name: cysteine monobromobimane derivative
-def: "modification from Unimod Chemical derivative" [PubMed:7856876, Unimod:301]
-comment: 1-(bromomethyl)-2,6,7-trimethylpyrazolo[1,2-a]pyrazole-3,5-dione, C 10 H 11 Br 1 N 2 O 2.
-synonym: "Bromobimane" RELATED PSI-MS-label []
-synonym: "Monobromobimane derivative" RELATED Unimod-description []
-property_value: DiffAvg "190.20" xsd:float
-property_value: DiffFormula "C 10 H 10 N 2 O 2" xsd:string
-property_value: DiffMono "190.074228" xsd:float
-property_value: Formula "C 13 H 15 N 3 O 3 S 1" xsd:string
-property_value: MassAvg "293.34" xsd:float
-property_value: MassMono "293.083412" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:301
-is_a: MOD:00848
-is_a: MOD:00905
-
-[Term]
-id: MOD:00621
-name: menadione quinone derivative
-def: "modification from Unimod Chemical derivative" [PubMed:15939799, Unimod:302]
-synonym: "Menadione" RELATED Unimod-interim []
-synonym: "Menadione quinone derivative" RELATED Unimod-description []
-property_value: DiffAvg "170.17" xsd:float
-property_value: DiffFormula "C 11 H 6 O 2" xsd:string
-property_value: DiffMono "170.036779" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:302
-is_a: MOD:00848
-
-[Term]
-id: MOD:00622
-name: cysteine mercaptoethanol
-def: "modification from Unimod Chemical derivative" [DeltaMass:80, PubMed:12442261, Unimod:303]
-comment: From DeltaMass: Average Mass: 76 Average Mass Change:76 PubMed:8019414.
-synonym: "Beta mercaptoethanol adduct" EXACT DeltaMass-label []
-synonym: "Cysteine mercaptoethanol" RELATED Unimod-description []
-synonym: "DeStreak" RELATED PSI-MS-label []
-property_value: DiffAvg "76.11" xsd:float
-property_value: DiffFormula "C 2 H 4 O 1 S 1" xsd:string
-property_value: DiffMono "75.998286" xsd:float
-property_value: Formula "C 5 H 9 N 1 O 2 S 2" xsd:string
-property_value: MassAvg "179.25" xsd:float
-property_value: MassMono "179.007471" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:303
-is_a: MOD:00848
-is_a: MOD:00905
-
-[Term]
-id: MOD:00623
-name: fucosylated biantennary (-2 galactose) N4-glycosylated asparagine
-def: "modification from Unimod N-linked glycosylation" [Unimod:305]
-synonym: "dHex(1)Hex(3)HexNAc(4)" RELATED PSI-MS-label []
-synonym: "Fucosylated biantennary (-2 galactose)" RELATED Unimod-description []
-property_value: DiffAvg "1443.33" xsd:float
-property_value: DiffFormula "C 56 H 90 N 4 O 39" xsd:string
-property_value: DiffMono "1442.518219" xsd:float
-property_value: Formula "C 60 H 96 N 6 O 41" xsd:string
-property_value: MassAvg "1557.43" xsd:float
-property_value: MassMono "1556.561147" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:305
-xref: GNO:G25987BV
-is_a: MOD:00725
-is_a: MOD:00160
-
-[Term]
-id: MOD:00624
-name: residues isobaric at 113.0-113.1 Da
-def: "Natural or modified residues with a mass of 113.0-113.1 Da." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:00616
-
-[Term]
-id: MOD:00625
-name: N-methylmaleimide derivatized residue
-def: "modification from Unimod Chemical derivative" [Unimod:314]
-synonym: "Nmethylmaleimide" RELATED PSI-MS-label []
-synonym: "Nmethylmaleimide" RELATED Unimod-description []
-property_value: DiffAvg "111.10" xsd:float
-property_value: DiffFormula "C 5 H 5 N 1 O 2" xsd:string
-property_value: DiffMono "111.032028" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:314
-is_a: MOD:00848
-
-[Term]
-id: MOD:00626
-name: fluorescein-5-thiosemicarbazide modified residue
-def: "modification from Unimod Chemical derivative" [PubMed:2883911, Unimod:478]
-synonym: "fluorescein-5-thiosemicarbazide" RELATED Unimod-description []
-synonym: "FTC" RELATED PSI-MS-label []
-property_value: DiffAvg "421.43" xsd:float
-property_value: DiffFormula "C 21 H 15 N 3 O 5 S 1" xsd:string
-property_value: DiffMono "421.073242" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:478
-is_a: MOD:00848
-
-[Term]
-id: MOD:00627
-name: 2,5-dimethylpyrrole lysine from 2,5-hexanedione adduct
-def: "modification from Unimod Chemical derivative" [Unimod:316]
-comment: There is no citation for this Unimod entry. Add PubMed:7981420, correct spelling [JSG].
-synonym: "(2S)-2-amino-6-(2,5-dimethylpyrrolidin-1-yl)hexanoic acid" EXACT PSI-MOD-alternate []
-synonym: "2,5-dimethypyrrole" RELATED Unimod-description []
-synonym: "6-(2,5-dimethylpyrrolidin-1-yl)norleucine" EXACT PSI-MOD-alternate []
-synonym: "DimethylpyrroleAdduct" RELATED PSI-MS-label []
-property_value: DiffAvg "78.11" xsd:float
-property_value: DiffFormula "C 6 H 6" xsd:string
-property_value: DiffMono "78.046950" xsd:float
-property_value: Formula "C 12 H 18 N 2 O 1" xsd:string
-property_value: MassAvg "206.29" xsd:float
-property_value: MassMono "206.141913" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:316
-is_a: MOD:00848
-is_a: MOD:00912
-
-[Term]
-id: MOD:00628
-name: Hex2
-def: "a protein modification that effectively replaces a hydrogen atom of an amino acid residue or of a modifying group with two hexose sugar groups through glycosidic bonds" [PubMed:18688235]
-property_value: DiffAvg "324.28" xsd:float
-property_value: DiffFormula "C 12 H 20 O 10" xsd:string
-property_value: DiffMono "324.105647" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-xref: GNO:G90627TW
-is_a: MOD:00725
-
-[Term]
-id: MOD:00629
-name: MDA adduct +62
-def: "modification from Unimod Chemical derivative" [Unimod:318]
-comment: Usually major adduct formed from malondialdehyde (MDA) with the amino group of lysine residues [UniProt].
-synonym: "Delta:H(2)C(5)" RELATED PSI-MS-label []
-synonym: "MDA adduct +62" RELATED Unimod-description []
-property_value: DiffAvg "62.07" xsd:float
-property_value: DiffFormula "C 5 H 2" xsd:string
-property_value: DiffMono "62.015650" xsd:float
-property_value: Formula "C 11 H 14 N 2 O 1" xsd:string
-property_value: MassAvg "190.25" xsd:float
-property_value: MassMono "190.110613" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:318
-is_a: MOD:00848
-is_a: MOD:00912
-
-[Term]
-id: MOD:00630
-name: C3-H2-O adduct (+54 amu) of malondialdehyde with lysine or methylglyoxal with arginine.
-def: "modification from Unimod Chemical derivative" [PubMed:9328283, Unimod:319]
-comment: This is not a legitimate ontological entry and will become obsolete when the children are reassigned [JSG]
-synonym: "Delta:H(2)C(3)O(1)" RELATED PSI-MS-label []
-synonym: "MDA adduct +54" RELATED Unimod-description []
-property_value: DiffAvg "54.05" xsd:float
-property_value: DiffFormula "C 3 H 2 O 1" xsd:string
-property_value: DiffMono "54.010565" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:319
-is_a: MOD:00848
-
-[Term]
-id: MOD:00631
-name: hydrolyzed N-ethylmaleimide adduct
-def: "modification from Unimod Chemical derivative" [Unimod:320]
-comment: N-ethylmaeimide adduct + H20 (a mixture of isobaric products) [JSG].
-synonym: "Nethylmaleimide+water" RELATED PSI-MS-label []
-synonym: "Nethylmaleimidehydrolysis" RELATED Unimod-description []
-property_value: DiffAvg "143.14" xsd:float
-property_value: DiffFormula "C 6 H 9 N 1 O 3" xsd:string
-property_value: DiffMono "143.058243" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:320
-is_a: MOD:00848
-
-[Term]
-id: MOD:00632
-name: N-succinimide
-def: "OBSOLETE because this chemical derivative modification from Unimod 321 is deprecated." [Unimod:321]
-property_value: DiffAvg "-17.01" xsd:float
-property_value: DiffFormula "H -1 O -1" xsd:string
-property_value: DiffMono "-17.002740" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:321
-is_obsolete: true
-
-[Term]
-id: MOD:00633
-name: bis-N-I-sulfonerahodamine
-def: "modification from Unimod Chemical derivative" [Unimod:323]
-comment: Invitrogen B-10621, a red fluorescent cross-linking reagent (only link to Cys is indicated) [Unimod].
-synonym: "bis-((N-iodoacetyl)piperazinyl)sulfonerhodamine" EXACT PSI-MOD-alternate []
-synonym: "bis-N-I-sulfonerahodamine" RELATED Unimod-description []
-synonym: "Xlink:B10621" RELATED PSI-MS-label []
-property_value: DiffAvg "713.57" xsd:float
-property_value: DiffFormula "C 31 H 30 I 1 N 4 O 6 S 1" xsd:string
-property_value: DiffMono "713.093078" xsd:float
-property_value: Formula "C 34 H 35 I 1 N 5 O 7 S 2" xsd:string
-property_value: MassAvg "816.71" xsd:float
-property_value: MassMono "816.102263" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:323
-is_a: MOD:00848
-is_a: MOD:00905
-
-[Term]
-id: MOD:00634
-name: dimethyl 3,3'-dithiobispropionimidate
-def: "modification from Unimod Chemical derivative" [PubMed:770170, Unimod:324]
-comment: Pierce reagent, needs sites for N, Q, R, K, and N-term [JSG].
-synonym: "dimethyl 3,3'-dithiobispropionimidate" RELATED Unimod-description []
-synonym: "DTBP" RELATED Unimod-interim []
-property_value: DiffAvg "123.60" xsd:float
-property_value: DiffFormula "C 3 Cl 1 H 6 N 1 S 1" xsd:string
-property_value: DiffMono "122.990948" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:324
-is_a: MOD:00848
-
-[Term]
-id: MOD:00635
-name: 10-fluoroethoxyphosphinyl-N-(biotinamidopentyl)decanamide
-def: "modification from Unimod Chemical derivative" [PubMed:10611275, Unimod:325]
-synonym: "10-ethoxyphosphinyl-N-(biotinamidopentyl)decanamide" RELATED Unimod-description []
-synonym: "FP-Biotin" RELATED Unimod-interim []
-property_value: DiffAvg "572.75" xsd:float
-property_value: DiffFormula "C 27 H 49 N 4 O 5 P 1 S 1" xsd:string
-property_value: DiffMono "572.316128" xsd:float
-property_value: Formula "C 30 H 54 N 5 O 7 P 1 S 1" xsd:string
-property_value: MassAvg "659.82" xsd:float
-property_value: MassMono "659.348157" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:325
-is_a: MOD:00848
-is_a: MOD:00861
-is_a: MOD:00916
-
-[Term]
-id: MOD:00636
-name: S-ethylcysteine (Ser)
-def: "A protein modification that effectively converts an L-serine residue to S-ethylcysteine." [Unimod:327]
-comment: Modification from Unimod. Phosphoserine is converted to dehydroalanine then by Michael addition of ethanethiol to S-ethylcysteine. Needs parent and sibling for S-ethyl-cysteine.
-synonym: "Delta:H(4)C(2)O(-1)S(1)" RELATED PSI-MS-label []
-synonym: "S-Ethylcystine from Serine" RELATED Unimod-description []
-property_value: DiffAvg "44.11" xsd:float
-property_value: DiffFormula "C 2 H 4 O -1 S 1" xsd:string
-property_value: DiffMono "44.008457" xsd:float
-property_value: Formula "C 5 H 9 N 1 O 1 S 1" xsd:string
-property_value: MassAvg "131.19" xsd:float
-property_value: MassMono "131.040485" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:327
-is_a: MOD:00916
-
-[Term]
-id: MOD:00637
-name: 1x(13)C,3x(2)H labeled monomethylated L-arginine
-def: "A protein modification that effectively replaces one hydrogen atom of an L-arginine residue with a (13)C,3x(2)H labeled methyl group to form a 1x(13)C,3x(2)H labeled monomethylated L-arginine." [Unimod:329]
-synonym: "Methyl:2H(3)13C(1)" RELATED PSI-MS-label []
-synonym: "monomethylated arginine" RELATED Unimod-description []
-property_value: DiffAvg "18.04" xsd:float
-property_value: DiffFormula "(13)C 1 (1)H -1 (2)H 3" xsd:string
-property_value: DiffMono "18.037835" xsd:float
-property_value: Formula "(12)C 6 (13)C 1 (1)H 11 (2)H 3 N 4 O 1" xsd:string
-property_value: MassAvg "174.14" xsd:float
-property_value: MassMono "174.138946" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:329
-is_a: MOD:00839
-is_a: MOD:00842
-is_a: MOD:00902
-relationship: derives_from MOD:00414
-
-[Term]
-id: MOD:00638
-name: 2x(13)C,6x(2)H labeled dimethylated L-arginine
-def: "A protein modification that effectively replaces two hydrogen atoms of an L-arginine residue with two (13)C,3x(2)H labeled methyl groups to form a 2x(13)C,6x(2)H labeled dimethylated L-arginine." [PubMed:15782174, Unimod:330]
-synonym: "Dimethyl:2H(6)13C(2)" RELATED PSI-MS-label []
-synonym: "dimethylated arginine" RELATED Unimod-description []
-property_value: DiffAvg "36.08" xsd:float
-property_value: DiffFormula "(13)C 2 (1)H -2 (2)H 6" xsd:string
-property_value: DiffMono "36.075670" xsd:float
-property_value: Formula "(12)C 6 (13)C 2 (1)H 10 (2)H 6 N 4 O 1" xsd:string
-property_value: MassAvg "192.18" xsd:float
-property_value: MassMono "192.176781" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:330
-is_a: MOD:00839
-is_a: MOD:00842
-is_a: MOD:00902
-relationship: derives_from MOD:00783
-
-[Term]
-id: MOD:00639
-name: thiophosphate labeled with biotin-HPDP
-def: "modification from Unimod Chemical derivative" [Unimod:332]
-synonym: "Thiophos-S-S-biotin" RELATED PSI-MS-label []
-synonym: "thiophosphate labeled with biotin-HPDP" RELATED Unimod-description []
-property_value: DiffAvg "525.66" xsd:float
-property_value: DiffFormula "C 19 H 34 N 4 O 5 P 1 S 3" xsd:string
-property_value: DiffMono "525.142895" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:332
-is_a: MOD:00848
-is_a: MOD:00861
-
-[Term]
-id: MOD:00640
-name: 6-N-biotinylaminohexyl isopropyl phosphorofluoridate
-def: "modification from Unimod Chemical derivative" [Unimod:333]
-synonym: "6-N-biotinylaminohexyl isopropyl phosphate" RELATED Unimod-description []
-synonym: "Can-FP-biotin" RELATED Unimod-interim []
-property_value: DiffAvg "467.54" xsd:float
-property_value: DiffFormula "C 19 F 1 H 35 N 3 O 5 P 1 S 1" xsd:string
-property_value: DiffMono "467.201907" xsd:float
-property_value: Formula "C 22 F 1 H 40 N 4 O 7 P 1 S 1" xsd:string
-property_value: MassAvg "554.62" xsd:float
-property_value: MassMono "554.233935" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:333
-is_a: MOD:00848
-is_a: MOD:00861
-is_a: MOD:00916
-
-[Term]
-id: MOD:00641
-name: CAMthiopropanoyl of Lys
-def: "OBSOLETE because Unimod entry 334 is merged with Unimod 293. Remap to MOD:00612" [Unimod:334]
-property_value: DiffAvg "146.18" xsd:float
-property_value: DiffFormula "C 5 H 8 N 1 O 2 S 1" xsd:string
-property_value: DiffMono "146.027574" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-replaced_by: MOD:00612
-xref: Unimod:334
-is_obsolete: true
-
-[Term]
-id: MOD:00642
-name: reduced 4-hydroxynonenal adduct
-def: "A protein modification produced by formation of an adduct of a residue with 4-hydroxynonenal artificially reduced by a reagent such as NaBH4." [PubMed:11910026, PubMed:15133838, Unimod:335]
-comment: 4-hydroxynonenal, a toxic lipid aldehyde, is a product of the hydroperoxide beta-cleavage degradation of omega-6 polyunsaturated fatty acids, such as arachidonic and linoleic acids [JSG].
-synonym: "HNE+Delta:H(2)" RELATED PSI-MS-label []
-synonym: "reduced 4-Hydroxynonenal" RELATED Unimod-description []
-property_value: DiffAvg "158.24" xsd:float
-property_value: DiffFormula "C 9 H 18 O 2" xsd:string
-property_value: DiffMono "158.130680" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:335
-is_a: MOD:00848
-is_a: MOD:01155
-relationship: derives_from MOD:00446
-
-[Term]
-id: MOD:00643
-name: methylamine Michael addition derivatized residue
-def: "modification from Unimod Artifact" [PubMed:11968134, Unimod:337]
-synonym: "Methylamine" RELATED PSI-MS-label []
-synonym: "Michael addition with methylamine" RELATED Unimod-description []
-property_value: DiffAvg "13.04" xsd:float
-property_value: DiffFormula "C 1 H 3 N 1 O -1" xsd:string
-property_value: DiffMono "13.031634" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:337
-is_a: MOD:00848
-
-[Term]
-id: MOD:00644
-name: mono O-acetylated residue
-def: "A protein modification that effectively replaces a residue hydroxyl group with an acetoxy group." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "OAcRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 2 H 2 O 1" xsd:string
-property_value: DiffMono "42.010565" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00394
-is_a: MOD:00671
-
-[Term]
-id: MOD:00645
-name: mono S-acetylated residue
-def: "A protein modification that effectively replaces a residue sulfanyl group with an acetylsulfanyl group." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "SAcRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 2 H 2 O 1 S 0" xsd:string
-property_value: DiffMono "42.010565" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00394
-is_a: MOD:00672
-
-[Term]
-id: MOD:00646
-name: monoacetylated L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to either N-acetyl-L-cysteine or S-acetyl-L-cysteine." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "AcCys" EXACT PSI-MOD-label []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 2 H 2 N 0 O 1 S 0" xsd:string
-property_value: DiffMono "42.010565" xsd:float
-property_value: Formula "C 5 H 7 N 1 O 2 S 1" xsd:string
-property_value: MassAvg "145.18" xsd:float
-property_value: MassMono "145.019749" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00394
-is_a: MOD:00905
-
-[Term]
-id: MOD:00647
-name: monoacetylated L-serine
-def: "A protein modification that effectively converts an L-serine residue to either N-acetyl-L-serine, O-acetyl-L-serine, or N,O-diacetyl-L-serine." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "AcSer" EXACT PSI-MOD-label []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 2 H 2 N 0 O 1" xsd:string
-property_value: DiffMono "42.010565" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00394
-is_a: MOD:00916
-
-[Term]
-id: MOD:00648
-name: N,O-diacetylated L-serine
-def: "A protein modification that effectively converts an L-serine residue to N,O-diacetyl-L-serine." [PubMed:16731519, PubMed:489587, PubMed:7309355, RESID:AA0051#var, RESID:AA0364#var]
-comment: In one paper, the samples were prepared using glacial acetic acid, and were probably artifactual [JSG].
-synonym: "(S)-2-acetamido-3-acetyloxypropanoic acid" EXACT PSI-MOD-alternate []
-synonym: "N,O-diacetyl-L-serine" EXACT PSI-MOD-alternate []
-synonym: "N,O-diacetylserine" EXACT PSI-MOD-alternate []
-synonym: "NOAc2Ser" EXACT PSI-MOD-label []
-property_value: DiffAvg "84.07" xsd:float
-property_value: DiffFormula "C 4 H 4 N 0 O 2" xsd:string
-property_value: DiffMono "84.021129" xsd:float
-property_value: Formula "C 7 H 10 N 1 O 4" xsd:string
-property_value: MassAvg "172.16" xsd:float
-property_value: MassMono "172.060983" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:02080
-relationship: has_functional_parent MOD:00060
-relationship: has_functional_parent MOD:00369
-
-[Term]
-id: MOD:00649
-name: acylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with an acyl group." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "AcylRes" EXACT PSI-MOD-label []
-is_a: MOD:01156
-
-[Term]
-id: MOD:00650
-name: N-myristoylated residue
-def: "A protein modification that effectively replaces a residue amino group with a myristoylamino group." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "NMyrRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "210.36" xsd:float
-property_value: DiffFormula "C 14 H 26 O 1" xsd:string
-property_value: DiffMono "210.198365" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00438
-is_a: MOD:00670
-
-[Term]
-id: MOD:00651
-name: N-palmitoylated residue
-def: "A protein modification that effectively replaces a residue amino group with a palmitoylamino group." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "NPamRes" EXACT PSI-MOD-label []
-synonym: "N-hexadecanoylated residue" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "238.41" xsd:float
-property_value: DiffFormula "C 16 H 30 O 1" xsd:string
-property_value: DiffMono "238.229666" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00440
-is_a: MOD:00670
-
-[Term]
-id: MOD:00652
-name: O-palmitoylated residue
-def: "A protein modification that effectively replaces a residue hydroxyl group with a palmitoyloxy group." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "OPamRes" EXACT PSI-MOD-label []
-synonym: "O-hexadecanoylated residue" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "238.41" xsd:float
-property_value: DiffFormula "C 16 H 30 O 1" xsd:string
-property_value: DiffMono "238.229666" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00440
-is_a: MOD:00671
-
-[Term]
-id: MOD:00653
-name: S-palmitoylated residue
-def: "A protein modification that effectively replaces a residue sulfanyl group with an palmitoylsulfanyl group." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "SPamRes" EXACT PSI-MOD-label []
-synonym: "S-hexadecanoylated residue" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "238.41" xsd:float
-property_value: DiffFormula "C 16 H 30 O 1 S 0" xsd:string
-property_value: DiffMono "238.229666" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00440
-is_a: MOD:00672
-
-[Term]
-id: MOD:00654
-name: S-methylated residue
-def: "a protein modification that effectively replaces a sulfanyl group with a methylsulfanyl group" [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "SMeRes" EXACT PSI-MOD-label []
-is_a: MOD:00427
-
-[Term]
-id: MOD:00655
-name: S-myristoylated residue
-def: "A protein modification that effectively replaces a residue sulfanyl group with an myristoylsulfanyl group." [PubMed:18688235]
-synonym: "SMyrRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "210.36" xsd:float
-property_value: DiffFormula "C 14 H 26 O 1 S 0" xsd:string
-property_value: DiffMono "210.198365" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00438
-is_a: MOD:00672
-
-[Term]
-id: MOD:00656
-name: C-methylated residue
-def: "A protein modification that effectively replaces a residue hydrocarbyl hydrogen with an methyl group." [PubMed:18688235]
-synonym: "CMeRes" EXACT PSI-MOD-label []
-is_a: MOD:00427
-
-[Term]
-id: MOD:00657
-name: L-glutamic acid 5-methyl ester (Gln)
-def: "A protein modification that effectively converts an L-glutamine residue to L-glutamate 5-methyl ester." [PubMed:16888, PubMed:6300110, RESID:AA0072#GLN, Unimod:528]
-comment: This is known to be a natural modification of glutamine in prokaryotes.
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-5-methoxy-5-oxopentanoic acid" EXACT RESID-systematic []
-synonym: "(5)-methyl L-hydrogen glutamate" EXACT RESID-alternate []
-synonym: "2-aminopentanedioic acid 5-methyl ester" EXACT RESID-alternate []
-synonym: "5-methyl L-2-aminoglutarate" EXACT RESID-alternate []
-synonym: "5-methyl L-glutamate" EXACT RESID-alternate []
-synonym: "deamidated 5-methyl esterified glutamine" EXACT PSI-MOD-alternate []
-synonym: "Deamidation followed by a methylation" RELATED Unimod-description []
-synonym: "glutamic acid 5-methyl ester" EXACT RESID-alternate []
-synonym: "glutamic acid gamma-methyl ester" EXACT RESID-alternate []
-synonym: "L-glutamic acid 5-methyl ester" EXACT RESID-name []
-synonym: "Methyl+Deamidated" RELATED PSI-MS-label []
-synonym: "MOD_RES Glutamate methyl ester (Gln)" EXACT UniProt-feature []
-synonym: "O5MeGlu(Gln)" EXACT PSI-MOD-label []
-property_value: DiffAvg "15.01" xsd:float
-property_value: DiffFormula "C 1 H 1 N -1 O 1" xsd:string
-property_value: DiffMono "14.999666" xsd:float
-property_value: Formula "C 6 H 9 N 1 O 3" xsd:string
-property_value: MassAvg "143.14" xsd:float
-property_value: MassMono "143.058243" xsd:float
-property_value: Origin "Q" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:528
-xref: uniprot.ptm:PTM-0127
-is_a: MOD:01369
-is_a: MOD:01453
-relationship: has_functional_parent MOD:00659
-
-[Term]
-id: MOD:00658
-name: methylated arginine
-def: "A protein modification that effectively converts an L-arginine residue to a methylated arginine, either 5-methylargine, N5-methylarginine, or an omega-N-methylated L-arginine." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "MeArg" EXACT PSI-MOD-label []
-property_value: Origin "R" xsd:string
-xref: uniprot.ptm:PTM-0238
-is_a: MOD:00427
-is_a: MOD:00902
-
-[Term]
-id: MOD:00659
-name: methylated glutamine
-def: "A protein modification that effectively converts an L-glutamine residue to a methylated glutamine, either 2-methylated glutamine, N5-methylated glutamine, or methyl esterified deamidated glutamine." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "MeGln" EXACT PSI-MOD-label []
-property_value: Origin "Q" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00427
-is_a: MOD:00907
-
-[Term]
-id: MOD:00660
-name: methylated cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to a methylated cysteine, either S-methylcysteine, or cysteine methyl ester." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "MeCys" EXACT PSI-MOD-label []
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00427
-is_a: MOD:00905
-
-[Term]
-id: MOD:00661
-name: methylated histidine
-def: "A protein modification that effectively converts an L-histidine residue to a methylated histidine, such as pros-methylhistidine, or tele-methylhistidine." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "MeHis" EXACT PSI-MOD-label []
-property_value: Origin "H" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00427
-is_a: MOD:00909
-
-[Term]
-id: MOD:00662
-name: methylated leucine
-def: "A protein modification that effectively converts an L-leucine residue to a methylated leucine, either N-methylleucine, or leucine methyl ester." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "MeLeu" EXACT PSI-MOD-label []
-property_value: Origin "L" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00427
-is_a: MOD:00911
-
-[Term]
-id: MOD:00663
-name: methylated lysine
-def: "A protein modification that effectively converts an L-lysine residue to a methylated lysine." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "MeLys" EXACT PSI-MOD-label []
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0193
-is_a: MOD:00427
-is_a: MOD:00912
-
-[Term]
-id: MOD:00664
-name: stereoisomerized residue
-def: "A protein modification that effectively replaces a residue L-enantiomer (stereoisomer) with a D-enantiomer or with a different diastereomeric isomer." [PubMed:18688235]
-synonym: "D-Res" EXACT PSI-MOD-label []
-is_a: MOD:01156
-
-[Term]
-id: MOD:00665
-name: methylated alanine
-def: "A protein modification that effectively converts an L-alanine residue to a methylated alanine, such as N-methylalanine, N,N-dimethylalanine, or N,N,N-trimethylalanine." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "MeAla" EXACT PSI-MOD-label []
-property_value: Origin "A" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00427
-is_a: MOD:00901
-
-[Term]
-id: MOD:00666
-name: octanoylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with an octanoyl group." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "OctRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "126.20" xsd:float
-property_value: DiffFormula "C 8 H 14 N 0 O 1" xsd:string
-property_value: DiffMono "126.104465" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00649
-is_a: MOD:01155
-
-[Term]
-id: MOD:00667
-name: decanoylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with a decanoyl group." [PubMed:18688235]
-synonym: "DecRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "154.25" xsd:float
-property_value: DiffFormula "C 10 H 18 N 0 O 1" xsd:string
-property_value: DiffMono "154.135765" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00649
-is_a: MOD:01155
-
-[Term]
-id: MOD:00668
-name: O-decanoylated residue
-def: "A protein modification that effectively replaces a residue hydroxyl group with a decanoyloxy group." [Unimod:449]
-synonym: "Decanoyl" RELATED PSI-MS-label []
-synonym: "lipid" RELATED Unimod-description []
-synonym: "ODecRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "154.25" xsd:float
-property_value: DiffFormula "C 10 H 18 N 0 O 1" xsd:string
-property_value: DiffMono "154.135765" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:449
-is_a: MOD:00667
-is_a: MOD:00671
-
-[Term]
-id: MOD:00669
-name: O-octanoylated residue
-def: "A protein modification that effectively replaces a residue hydroxyl group with a octanoyloxy group." [Unimod:426]
-subset: PSI-MOD-slim
-synonym: "Octanoyl" RELATED PSI-MS-label []
-synonym: "octanoyl" RELATED Unimod-description []
-synonym: "OOctRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "126.20" xsd:float
-property_value: DiffFormula "C 8 H 14 N 0 O 1" xsd:string
-property_value: DiffMono "126.104465" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:426
-is_a: MOD:00666
-is_a: MOD:00671
-
-[Term]
-id: MOD:00670
-name: N-acylated residue
-def: "A protein modification that effectively replaces a residue alpha-amino- or alpha-imino-hydrogen with an acyl group." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "NAcylRes" EXACT PSI-MOD-label []
-is_a: MOD:00649
-
-[Term]
-id: MOD:00671
-name: O-acylated residue
-def: "A protein modification that effectively replaces a residue hydroxyl group with a acyloxy group." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "OAcylRes" EXACT PSI-MOD-label []
-is_a: MOD:00649
-
-[Term]
-id: MOD:00672
-name: S-acylated residue
-def: "A protein modification that effectively replaces a residue sulfanyl group with an acylsulfanyl group." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "SAcylRes" EXACT PSI-MOD-label []
-is_a: MOD:00649
-
-[Term]
-id: MOD:00673
-name: methylated asparagine
-def: "A protein modification that effectively converts an L-asparagine residue to a methylated asparagine, such as N4-methyl-L-asparagine, or N4,N4-dimethyl-L-asparagine." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "MeAsn" EXACT PSI-MOD-label []
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00427
-is_a: MOD:00903
-
-[Term]
-id: MOD:00674
-name: amidated residue
-def: "A protein modification that effectively replaces a carboxyl group with a carboxamido group." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: DiffAvg "-0.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 1 O -1" xsd:string
-property_value: DiffMono "-0.984016" xsd:float
-property_value: Origin "X" xsd:string
-is_a: MOD:01156
-
-[Term]
-id: MOD:00675
-name: oxidized residue
-def: "A protein modification that effectively either removes neutral hydrogen atoms (proton and electron), or adds oxygen atoms to a residue with or without the removal of hydrogen atoms." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "OxRes" EXACT PSI-MOD-label []
-property_value: Origin "X" xsd:string
-is_a: MOD:01156
-
-[Term]
-id: MOD:00676
-name: oxygenated residue
-def: "A protein modification that effectively adds oxygen atoms to a residue with or without the removal of hydrogen atoms." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "OxyRes" EXACT PSI-MOD-label []
-property_value: Origin "X" xsd:string
-is_a: MOD:00675
-
-[Term]
-id: MOD:00677
-name: hydroxylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with an hydroxyl group." [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 16
-subset: PSI-MOD-slim
-synonym: "Hydroxylation (of delta C of Lysine, beta C of Tryptophan, C3 or C4 of Proline, beta C of Aspartate)" EXACT DeltaMass-label []
-synonym: "HyRes" EXACT PSI-MOD-label []
-property_value: Origin "X" xsd:string
-is_a: MOD:00679
-
-[Term]
-id: MOD:00678
-name: hydroxylated proline
-def: "A protein modification that effectively converts an L-proline residue to an hydroxylated L-proline." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "HyPro" EXACT PSI-MOD-label []
-property_value: Origin "P" xsd:string
-is_a: MOD:00677
-is_a: MOD:00915
-
-[Term]
-id: MOD:00679
-name: carbon oxygenated residue
-def: "A protein modification that effectively adds oxygen atoms to a carbon atom of a residue and removes hydrogen atoms." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "COxyRes" EXACT PSI-MOD-label []
-is_a: MOD:00676
-
-[Term]
-id: MOD:00680
-name: sulfur oxygenated residue
-def: "A protein modification that effectively adds oxygen atoms to a sulfur atom of a residue without removing hydrogen atoms." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "SOxyRes" EXACT PSI-MOD-label []
-is_a: MOD:00676
-
-[Term]
-id: MOD:00681
-name: hydroxylated lysine
-def: "A protein modification that effectively converts an L-lysine residue to a hydroxylated L-lysine." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "HyLys" EXACT PSI-MOD-label []
-property_value: Origin "K" xsd:string
-is_a: MOD:00677
-is_a: MOD:00912
-
-[Term]
-id: MOD:00682
-name: hydroxylated arginine
-def: "A protein modification that effectively converts an L-arginine residue to a hydroxylated L-arginine." [PubMed:18688235]
-synonym: "HyArg" EXACT PSI-MOD-label []
-property_value: Origin "R" xsd:string
-xref: uniprot.ptm:PTM-0498
-is_a: MOD:00677
-is_a: MOD:00902
-
-[Term]
-id: MOD:00683
-name: dehydrogenated residue
-def: "A protein modification that effectively removes neutral hydrogen atoms (proton and electron) from a residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "dHRes" EXACT PSI-MOD-label []
-property_value: Origin "X" xsd:string
-is_a: MOD:00675
-
-[Term]
-id: MOD:00684
-name: deamidated L-asparagine
-def: "A protein modification that effectively converts an L-asparagine residue to L-aspartic acid." [PubMed:1097438, PubMed:339692, PubMed:4399050, PubMed:5764436, PubMed:6692818, PubMed:8089117, PubMed:9521123, PubMed:9582379, RESID:AA0004#ASN, Unimod:7#N]
-comment: incidental to RESID:AA0059
-subset: PSI-MOD-slim
-synonym: "(2S)-2-aminobutanedioic acid" EXACT RESID-systematic []
-synonym: "2-azanylbutanedioic acid" EXACT RESID-alternate []
-synonym: "aminosuccinic acid" EXACT RESID-alternate []
-synonym: "dNAsn" EXACT PSI-MOD-label []
-synonym: "L-aspartic acid" EXACT RESID-name []
-synonym: "MOD_RES Deamidated asparagine" EXACT UniProt-feature []
-property_value: DiffAvg "0.98" xsd:float
-property_value: DiffFormula "C 0 H -1 N -1 O 1" xsd:string
-property_value: DiffMono "0.984016" xsd:float
-property_value: Formula "C 4 H 5 N 1 O 3" xsd:string
-property_value: MassAvg "115.09" xsd:float
-property_value: MassMono "115.026943" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:7
-xref: uniprot.ptm:PTM-0116
-is_a: MOD:00400
-is_a: MOD:00903
-
-[Term]
-id: MOD:00685
-name: deamidated L-glutamine
-def: "A protein modification that effectively converts an L-glutamine residue to L-glutamic acid." [PubMed:1881881, PubMed:4565668, PubMed:4922541, PubMed:6692818, PubMed:9192900, PubMed:957425, RESID:AA0006#GLN, Unimod:7#Q]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-aminopentanedioic acid" EXACT RESID-systematic []
-synonym: "1-aminopropane-1,3-dicarboxylic acid" EXACT RESID-alternate []
-synonym: "2-aminoglutaric acid" EXACT RESID-alternate []
-synonym: "2-azanylpentanedioic acid" EXACT RESID-alternate []
-synonym: "alpha-aminoglutaric acid" EXACT RESID-alternate []
-synonym: "dNGln" EXACT PSI-MOD-label []
-synonym: "glutaminic acid" EXACT RESID-alternate []
-synonym: "L-glutamic acid" EXACT RESID-name []
-synonym: "MOD_RES Deamidated glutamine" EXACT UniProt-feature []
-property_value: DiffAvg "0.98" xsd:float
-property_value: DiffFormula "C 0 H -1 N -1 O 1" xsd:string
-property_value: DiffMono "0.984016" xsd:float
-property_value: Formula "C 5 H 7 N 1 O 3" xsd:string
-property_value: MassAvg "129.12" xsd:float
-property_value: MassMono "129.042593" xsd:float
-property_value: Origin "Q" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:7
-xref: uniprot.ptm:PTM-0117
-is_a: MOD:00400
-is_a: MOD:00907
-
-[Term]
-id: MOD:00686
-name: L-selenocysteine (Cys)
-def: "A protein modification that effectively converts an L-cysteine residue to L-selenocysteine (not known as a natural, post-translational modification process)." [PubMed:10523135, PubMed:2037562, PubMed:2963330, PubMed:6217842, PubMed:6714945, RESID:AA0022#CYS, Unimod:162#C]
-comment: This entry is for the artifactual formation of L-selenocysteine from cysteine. For encoded L-selenocysteine, use MOD:00031 [JSG].
-synonym: "(2R)-2-amino-3-selanylpropanoic acid" EXACT RESID-systematic []
-synonym: "2-azanyl-3-selanylpropanoic acid" EXACT RESID-alternate []
-synonym: "3-selenylalanine" EXACT RESID-alternate []
-synonym: "L-selenocysteine" EXACT RESID-name []
-synonym: "NON_STD Selenocysteine" EXACT UniProt-feature []
-synonym: "Sec(Cys)" EXACT PSI-MOD-label []
-synonym: "SeCys" EXACT RESID-alternate []
-synonym: "selenium cysteine" EXACT RESID-alternate []
-property_value: DiffAvg "46.91" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0 S -1 Se 1" xsd:string
-property_value: DiffMono "47.944450" xsd:float
-property_value: Formula "C 3 H 5 N 1 O 1 Se 1" xsd:string
-property_value: MassAvg "150.05" xsd:float
-property_value: MassMono "150.953635" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:162
-is_a: MOD:00007
-is_a: MOD:00905
-
-[Term]
-id: MOD:00687
-name: thioether crosslinked residues
-def: "A protein modification that crosslinks two residues by formation of a thioether bond between a cysteine thiol and either an alkyl C as in lanthionine, or an aryl C as 2'-(S-cysteinyl)-L-histidine." [PubMed:18688235]
-is_a: MOD:00033
-is_a: MOD:02044
-
-[Term]
-id: MOD:00688
-name: isopeptide crosslinked residues
-def: "A protein modification that crosslinks two residues with an amide bond where either the donor amino or carboxyl is not an alpha group." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:00033
-
-[Term]
-id: MOD:00689
-name: disulfide crosslinked residues
-def: "A protein modification that crosslinks two cysteine residues by formation of a disulfide bond." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:01619
-
-[Term]
-id: MOD:00690
-name: oxazole/thiazole ring crosslinked residues
-def: "A protein modification that crosslinks two residues by formation of an oxazole or thiazole ring." [PubMed:18688235]
-is_a: MOD:00033
-
-[Term]
-id: MOD:00691
-name: 5-imidazolinone ring crosslinked residues
-def: "A protein modification that crosslinks two residues by formation of an 5-imidazolinone ring." [PubMed:18688235]
-is_a: MOD:00033
-
-[Term]
-id: MOD:00692
-name: uncategorized crosslinked residues
-def: "A protein crosslink modification that is not chemically categorized." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:00033
-
-[Term]
-id: MOD:00693
-name: glycosylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with an carbohydrate-like group through a glycosidic bond." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "GlycoRes" EXACT PSI-MOD-label []
-property_value: Source "natural" xsd:string
-is_a: MOD:00764
-
-[Term]
-id: MOD:00694
-name: halogen containing residue
-def: "A protein modification that effectively substitutes a halogen atom for a hydrogen atom." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "halogenated residue" EXACT PSI-MOD-alternate []
-synonym: "HalRes" EXACT PSI-MOD-label []
-is_a: MOD:01156
-
-[Term]
-id: MOD:00695
-name: sulfated residue
-def: "A protein modification that effectively substitutes a sulfonyl group for the hydrogen atom of a hydroxyl or sulfanyl group." [DeltaMass:0, PubMed:14752058, Unimod:40]
-comment: From DeltaMass: Average Mass: 80.
-subset: PSI-MOD-slim
-synonym: "O-Sulfonation" RELATED Unimod-description []
-synonym: "Sulfo" RELATED PSI-MS-label []
-synonym: "SulfRes" EXACT PSI-MOD-label []
-synonym: "Sulphonation (SO3H) (of PMC group)" EXACT DeltaMass-label []
-property_value: DiffAvg "80.06" xsd:float
-property_value: DiffFormula "O 3 S 1" xsd:string
-property_value: DiffMono "79.956815" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:40
-is_a: MOD:00860
-
-[Term]
-id: MOD:00696
-name: phosphorylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with a phosphono group (H2PO3 or 'phosphate')." [DeltaMass:0, Unimod:21]
-comment: From DeltaMass: Average Mass: 80.
-subset: PSI-MOD-slim
-synonym: "Phospho" RELATED PSI-MS-label []
-synonym: "Phosphorylation" RELATED Unimod-description []
-synonym: "Phosphorylation (O of Serine, Threonine, Tyrosine and Aspartate, N epsilon of Lysine)" EXACT DeltaMass-label []
-synonym: "PhosRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "79.98" xsd:float
-property_value: DiffFormula "H 1 O 3 P 1" xsd:string
-property_value: DiffMono "79.966331" xsd:float
-property_value: Origin "X" xsd:string
-xref: Unimod:21
-is_a: MOD:00861
-
-[Term]
-id: MOD:00697
-name: flavin modified residue
-def: "A protein modification that effectively results from forming an adduct with a compound containing a flavin group." []
-subset: PSI-MOD-slim
-synonym: "FAD" RELATED PSI-MS-label []
-synonym: "Flavin adenine dinucleotide" RELATED Unimod-description []
-synonym: "FlavRes" EXACT PSI-MOD-label []
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:01156
-
-[Term]
-id: MOD:00698
-name: metal or metal cluster containing modified residue
-def: "A protein modification that effectively substitutes a metal atom or a metal cluster for hydrogen atoms, or coordinates a metal ion." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "MetalRes" EXACT PSI-MOD-label []
-is_a: MOD:01156
-
-[Term]
-id: MOD:00699
-name: porphyrin modified residue
-def: "A protein modification that effectively results from forming an adduct with a compound containing a porphyrin group." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "PorphRes" EXACT PSI-MOD-label []
-is_a: MOD:01156
-
-[Term]
-id: MOD:00700
-name: tetrapyrrole modified residue
-def: "A protein modification that effectively results from forming an adduct with a compound containing a tetrapyrrole group." [PubMed:18688235]
-synonym: "TetrapyrRes" EXACT PSI-MOD-label []
-is_a: MOD:01156
-
-[Term]
-id: MOD:00701
-name: nucleotide or nucleic acid modified residue
-def: "A protein modification that effectively results from forming an adduct with a compound containing a nucleotide or a polynucleotide through formation of either a phosphodiester bond, a phosphoramide ester bond, or a glycosidic bond." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "NucRes" EXACT PSI-MOD-label []
-is_a: MOD:01156
-
-[Term]
-id: MOD:00702
-name: isotope labeled residue
-def: "A protein modification that effectively substitutes atoms of particular common isotopes with atoms or groups containing isotopes that are not the most common." [PubMed:18688235]
-comment: In SILAC (stable isotope labelling of amino acids in cell culture), the label may be introduced either through labeling of an incorporated residue or labeling of the substrates in a metabolic modification. For isotope labeling introduced through a modification reagent see MOD:01426.
-subset: PSI-MOD-slim
-synonym: "IsoTagRes" EXACT PSI-MOD-label []
-synonym: "SILAC" EXACT PSI-MOD-alternate []
-is_a: MOD:01156
-
-[Term]
-id: MOD:00703
-name: isoprenylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with a group derived from an isoprene polymer, such as a geranyl (C10), farnesyl (C15) or geranylgeranyl (C20) group." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "IpRes" EXACT PSI-MOD-label []
-is_a: MOD:00001
-is_a: MOD:01155
-
-[Term]
-id: MOD:00704
-name: dehydrated residue
-def: "A protein modification that effectively forms a double bond by removing a molecule of water from a residue." [DeltaMass:0, Unimod:23]
-subset: PSI-MOD-slim
-synonym: "Dehydrated" RELATED Unimod-interim []
-synonym: "Dehydration" RELATED Unimod-description []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:23
-is_a: MOD:01156
-
-[Term]
-id: MOD:00705
-name: D-valine
-def: "A protein modification that effectively converts an L-valine residue to D-valine." [ChEBI:30016, PubMed:15853325, RESID:AA0200]
-synonym: "(R)-2-amino-3-methylbutanoic acid" EXACT RESID-systematic []
-synonym: "alpha-amino-beta-methylbutyric acid" EXACT RESID-alternate []
-synonym: "alpha-aminoisovaleric acid" EXACT RESID-alternate []
-synonym: "D-Val" EXACT PSI-MOD-label []
-synonym: "D-valine" EXACT RESID-name []
-synonym: "MOD_RES D-valine" EXACT UniProt-feature []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 5 H 9 N 1 O 1" xsd:string
-property_value: MassAvg "99.13" xsd:float
-property_value: MassMono "99.068414" xsd:float
-property_value: Origin "V" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0124
-is_a: MOD:00664
-
-[Term]
-id: MOD:00706
-name: dehydrogenated tyrosine
-def: "A protein modification that effectively converts L-tyrosine to 2,3-didehydrotyrosine." [Unimod:401#Y]
-subset: PSI-MOD-slim
-synonym: "dHTyr" EXACT PSI-MOD-label []
-synonym: "MOD_RES 2,3-didehydrotyrosine" EXACT UniProt-feature []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 9 H 7 N 1 O 2" xsd:string
-property_value: MassAvg "161.16" xsd:float
-property_value: MassMono "161.047678" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:401
-xref: uniprot.ptm:PTM-0008
-is_a: MOD:00919
-is_a: MOD:01888
-
-[Term]
-id: MOD:00707
-name: hydroxylated tyrosine
-def: "a protein modification that effectively converts an L-tyrosine residue to a multihydroxylated L-phenylalanine" [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "HyTyr" EXACT PSI-MOD-label []
-property_value: Origin "Y" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00677
-is_a: MOD:00919
-
-[Term]
-id: MOD:00708
-name: sulfur oxygenated L-cysteine
-def: "A protein modification that effectively adds oxygen atoms to a sulfur atom of L-cysteine residue without removing hydrogen atoms." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "SOxyCys" EXACT PSI-MOD-label []
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00680
-is_a: MOD:00905
-
-[Term]
-id: MOD:00709
-name: sulfur oxygenated L-methionine
-def: "A protein modification that effectively adds oxygen atoms to a sulfur atom of L-methionine residue without removing hydrogen atoms." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "SOxyMet" EXACT PSI-MOD-label []
-property_value: Origin "M" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00680
-is_a: MOD:00913
-
-[Term]
-id: MOD:00710
-name: protonated-dimethylated residue
-def: "A protein modification that effectively adds a proton and replaces two hydrogen atoms with two methyl groups." [PubMed:18688235]
-comment: For N-terminal proline residues, dimethylation can effectively only be accomplished with a protonated imino group. This process accounts for both protonation and dimethylation. The alternative Me2Res process accounts only for dimethylation and not protonation.
-subset: PSI-MOD-slim
-synonym: "Me2+Res" EXACT PSI-MOD-label []
-is_a: MOD:00429
-
-[Term]
-id: MOD:00711
-name: trimethylated protonated-residue
-def: "A protein modification that effectively replaces three hydrogen atoms with three methyl groups, after a proton has been added to form an aminium group." [PubMed:18688235]
-comment: For amino acids residues, amine trimethylation can effectively only be accomplished with a protonated primary amino group. This process accounts for both protonation and trimethylation. The alternative Me3Res process accounts only for trimethylation and not protonation.
-subset: PSI-MOD-slim
-synonym: "Me3+Res" EXACT PSI-MOD-label []
-property_value: DiffAvg "43.09" xsd:float
-property_value: DiffFormula "C 3 H 7 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "43.054227" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00427
-
-[Term]
-id: MOD:00712
-name: methylated proline
-def: "A protein modification that effectively converts an L-proline residue to a methylated proline, such as N,N-dimethylproline." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "MePro" EXACT PSI-MOD-label []
-property_value: Origin "P" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00427
-is_a: MOD:00915
-
-[Term]
-id: MOD:00713
-name: methylated glutamic acid
-def: "A protein modification that effectively converts an L-glutamic acid residue to a methylated glutamic acid, such as L-glutamate 5-methyl ester." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "MeGlu" EXACT PSI-MOD-label []
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00427
-is_a: MOD:00906
-
-[Term]
-id: MOD:00714
-name: methylated glycine
-def: "A protein modification that effectively converts a glycine residue to a methylated glycine, such as N-methylglycine." [PubMed:18688235]
-synonym: "MeGly" EXACT PSI-MOD-label []
-property_value: Origin "G" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00427
-is_a: MOD:00908
-
-[Term]
-id: MOD:00715
-name: methylated isoleucine
-def: "A protein modification that effectively converts an L-isoleucine residue to a methylated isoleucine residue, such as N-methyl-L-isoleucine." [PubMed:18688235]
-synonym: "MeIle" EXACT PSI-MOD-label []
-property_value: Origin "I" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00427
-is_a: MOD:00910
-
-[Term]
-id: MOD:00716
-name: methylated methionine
-def: "A protein modification that effectively converts an L-methionine residue to a methylated methionine, such as N-methyl-L-methionine." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "MeMet" EXACT PSI-MOD-label []
-property_value: Origin "M" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00427
-is_a: MOD:00913
-
-[Term]
-id: MOD:00717
-name: methylated phenylalanine
-def: "A protein modification that effectively converts an L-phenylalanine residue to a methylated phenylalanine, such as N-methyl-L-phenylalanine." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "MePhe" EXACT PSI-MOD-label []
-property_value: Origin "F" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00427
-is_a: MOD:00914
-
-[Term]
-id: MOD:00718
-name: methylated tyrosine
-def: "A protein modification that effectively converts an L-tyrosine residue to a methylated tyrosine, such as N-methyl-L-tyrosine." [PubMed:18688235]
-synonym: "MeTyr" EXACT PSI-MOD-label []
-property_value: Origin "Y" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00427
-is_a: MOD:00919
-
-[Term]
-id: MOD:00719
-name: L-methionine sulfoxide
-def: "A protein modification that oxygenates an L-methionine residue to one of the diastereomeric L-methionine sulfoxide residues." [DeltaMass:177, OMSSA:1, PubMed:21406390, PubMed:22116028, RESID:AA0581, Unimod:35#M]
-comment: From DeltaMass: Average Mass: 147 Formula:C5H9O1N2S Monoisotopic Mass Change:147.035 Average Mass Change:147.195 (formula incorrect, N and O reversed) References:PE Sciex.
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-4-[(R)-methylsulfinyl]butanoic acid" EXACT RESID-systematic []
-synonym: "L-methionine (R)-S-oxide" EXACT RESID-alternate []
-synonym: "L-methionine (R)-sulfoxide" EXACT RESID-name []
-synonym: "L-methionine S-oxide" EXACT PSI-MOD-alternate []
-synonym: "L-methionine sulfoxide" EXACT PSI-MOD-alternate []
-synonym: "Methionyl Sulfoxide" EXACT DeltaMass-label []
-synonym: "MetO" EXACT PSI-MOD-label []
-synonym: "MOD_RES Methionine sulfoxide" EXACT UniProt-feature []
-synonym: "Oxidation" RELATED PSI-MS-label []
-synonym: "oxym" EXACT OMSSA-label []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1 S 0" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 5 H 9 N 1 O 2 S 1" xsd:string
-property_value: MassAvg "147.19" xsd:float
-property_value: MassMono "147.035400" xsd:float
-property_value: Origin "M" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:35
-xref: uniprot.ptm:PTM-0469
-is_a: MOD:00709
-is_a: MOD:01854
-
-[Term]
-id: MOD:00720
-name: L-methionine (R)-sulfoxide
-def: "A protein modification that effectively oxygenates an L-methionine residue to L-methionine sulfoxide R-diastereomer." [ChEBI:45764, PubMed:21406390, PubMed:22116028, PubMed:23911929, RESID:AA0581]
-synonym: "(2S)-2-amino-4-[(R)-methylsulfinyl]butanoic acid" EXACT RESID-systematic []
-synonym: "L-methionine (R)-S-oxide" EXACT RESID-alternate []
-synonym: "L-methionine (R)-sulfoxide" EXACT RESID-name []
-synonym: "MOD_RES Methionine (R)-sulfoxide" EXACT UniProt-feature []
-synonym: "R-MetO" EXACT PSI-MOD-label []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1 S 0" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 5 H 9 N 1 O 2 S 1" xsd:string
-property_value: MassAvg "147.19" xsd:float
-property_value: MassMono "147.035400" xsd:float
-property_value: Origin "M" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0480
-is_a: MOD:00719
-
-[Term]
-id: MOD:00721
-name: L-methionine (S)-sulfoxide
-def: "A protein modification that effectively oxygenates an L-methionine residue to L-methionine sulfoxide S-diastereomer." [PubMed:18688235]
-synonym: "S-MetO" EXACT PSI-MOD-label []
-synonym: "MOD_RES Methionine (S)-sulfoxide" EXACT UniProt-feature []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1 S 0" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 5 H 9 N 1 O 2 S 1" xsd:string
-property_value: MassAvg "147.19" xsd:float
-property_value: MassMono "147.035400" xsd:float
-property_value: Origin "M" xsd:string
-property_value: Source "artifact" xsd:string
-xref: uniprot.ptm:PTM-0481
-is_a: MOD:00719
-
-[Term]
-id: MOD:00722
-name: monomethylated L-glutamine
-def: "A protein modification that effectively replaces one hydrogen atom of an L-glutamine residue with one methyl group." [OMSSA:14, Unimod:34#Q]
-subset: PSI-MOD-slim
-synonym: "Me1Gln" EXACT PSI-MOD-label []
-synonym: "methylq" EXACT OMSSA-label []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 6 H 10 N 2 O 2" xsd:string
-property_value: MassAvg "142.16" xsd:float
-property_value: MassMono "142.074228" xsd:float
-property_value: Origin "Q" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:34
-is_a: MOD:00599
-is_a: MOD:00659
-
-[Term]
-id: MOD:00723
-name: N-acetylated L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to either N2-acetyl-L-lysine, or N6-acetyl-L-lysine." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "NAcLys" EXACT PSI-MOD-label []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 2 H 2 N 0 O 1" xsd:string
-property_value: DiffMono "42.010565" xsd:float
-property_value: Formula "C 8 H 15 N 2 O 2" xsd:string
-property_value: MassAvg "171.22" xsd:float
-property_value: MassMono "171.113353" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00408
-is_a: MOD:00912
-
-[Term]
-id: MOD:00724
-name: N-methylated L-histidine
-def: "A protein modification that effectively replaces one hydrogen atom on a nitrogen of an L-histidine residue with one methyl group." [OMSSA:74, Unimod:34#H]
-subset: PSI-MOD-slim
-synonym: "Methyl" RELATED PSI-MS-label []
-synonym: "methylh" EXACT OMSSA-label []
-synonym: "NMeHis" EXACT PSI-MOD-label []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 7 H 9 N 3 O 1" xsd:string
-property_value: MassAvg "151.17" xsd:float
-property_value: MassMono "151.074562" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:34
-is_a: MOD:00599
-is_a: MOD:00602
-is_a: MOD:00661
-
-[Term]
-id: MOD:00725
-name: complex glycosylation
-def: "A protein modification that effectively replaces a hydrogen atom of an amino acid residue or of a modifying group with a carbohydrate-like group linked through a glycosidic bond." [PubMed:18688235]
-is_a: MOD:00693
-
-[Term]
-id: MOD:00726
-name: glucosylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of an amino acid residue or of a modifying group with a glucose group through a glycosidic bond." [PubMed:18688235]
-synonym: "Glc" EXACT PSI-MOD-label []
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-replaced_by: MOD:00433
-is_a: MOD:00693
-
-[Term]
-id: MOD:00727
-name: mannosylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of an amino acid residue or of a modifying group with a mannose group through a glycosidic bond," [PubMed:18688235]
-synonym: "Man" EXACT PSI-MOD-label []
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00693
-
-[Term]
-id: MOD:00728
-name: galactosylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of an amino acid residue or of a modifying group with a galactose group through a glycosidic bond." [PubMed:18688235]
-synonym: "Gal" EXACT PSI-MOD-label []
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00693
-
-[Term]
-id: MOD:00729
-name: pentosylated residue
-def: "a protein modification that effectively replaces a hydrogen atom of an amino acid residue or of a modifying group with a pentose sugar group through a glycosidic bond" [DeltaMass:172]
-comment: for Pentoses DeltaMass gives mass 132, for Pentosyl DeltaMass gives formula C 6 H 10 N4 with mass 146
-synonym: "Pent" EXACT PSI-MOD-label []
-synonym: "Pentoses (Ara, Rib, Xyl)" EXACT DeltaMass-label []
-synonym: "Pentosyl" EXACT DeltaMass-label []
-property_value: DiffAvg "132.12" xsd:float
-property_value: DiffFormula "C 5 H 8 O 4" xsd:string
-property_value: DiffMono "132.042259" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00693
-
-[Term]
-id: MOD:00730
-name: arabinosylated residue
-def: "a protein modification that effectively replaces a hydrogen atom of an amino acid residue or of a modifying group with a arabinose sugar group through a glycosidic bond" [PubMed:18688235]
-synonym: "Ara" EXACT PSI-MOD-label []
-property_value: DiffAvg "132.12" xsd:float
-property_value: DiffFormula "C 5 H 8 O 4" xsd:string
-property_value: DiffMono "132.042259" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00729
-
-[Term]
-id: MOD:00731
-name: ribosylated residue
-def: "a protein modification that effectively replaces a hydrogen atom of an amino acid residue or of a modifying group with a ribose sugar group through a glycosidic bond" [PubMed:18688235]
-synonym: "Rib" EXACT PSI-MOD-label []
-property_value: DiffAvg "132.12" xsd:float
-property_value: DiffFormula "C 5 H 8 O 4" xsd:string
-property_value: DiffMono "132.042259" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00729
-
-[Term]
-id: MOD:00732
-name: xylosylated residue
-def: "a protein modification that effectively replaces a hydrogen atom of an amino acid residue or of a modifying group with a xylose sugar group through a glycosidic bond" [PubMed:18688235]
-synonym: "Xyl" EXACT PSI-MOD-label []
-property_value: DiffAvg "132.12" xsd:float
-property_value: DiffFormula "C 5 H 8 O 4" xsd:string
-property_value: DiffMono "132.042259" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00729
-
-[Term]
-id: MOD:00733
-name: N-acetylaminoglucosylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of an amino acid residue or of a modifying group with an N-acetylglucosamine group through a glycosidic bond." [PubMed:18688235]
-synonym: "GlcNAc" EXACT PSI-MOD-label []
-property_value: DiffAvg "203.19" xsd:float
-property_value: DiffFormula "C 8 H 13 N 1 O 5" xsd:string
-property_value: DiffMono "203.079373" xsd:float
-property_value: Origin "X" xsd:string
-is_a: MOD:00436
-
-[Term]
-id: MOD:00734
-name: N-acetylaminogalactosylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of an amino acid residue or of a modifying group with an N-acetylgalactosamine group through a glycosidic bond." [DeltaMass:247]
-comment: From DeltaMass: Average Mass: 203 Formula:C8H13O5N1 Monoisotopic Mass Change:203.079 Average Mass Change:203.196 References:PE Sciex
-synonym: "GalNAc" EXACT PSI-MOD-label []
-synonym: "N-acetylhexosamines (GalNAc, GlcNAc)" EXACT DeltaMass-label []
-property_value: DiffAvg "203.19" xsd:float
-property_value: DiffFormula "C 8 H 13 N 1 O 5" xsd:string
-property_value: DiffMono "203.079373" xsd:float
-property_value: Origin "X" xsd:string
-is_a: MOD:00436
-
-[Term]
-id: MOD:00735
-name: hexosuronylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of an amino acid residue or of a modifying group with a hexosuronic acid group through a glycosidic bond." [PubMed:18688235]
-synonym: "HexA" EXACT PSI-MOD-label []
-property_value: DiffAvg "176.12" xsd:float
-property_value: DiffFormula "C 6 H 8 O 6" xsd:string
-property_value: DiffMono "176.032088" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00693
-
-[Term]
-id: MOD:00736
-name: deoxyhexosylated residue
-def: "a protein modification that effectively replaces a hydrogen atom of an amino acid residue or of a modifying group with a deoxyhexose group through a glycosidic bond" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 146
-subset: PSI-MOD-slim
-synonym: "Deoxyhexoses (Fuc, Rha)" EXACT DeltaMass-label []
-synonym: "dHex" EXACT PSI-MOD-label []
-property_value: DiffAvg "146.14" xsd:float
-property_value: DiffFormula "C 6 H 10 O 4" xsd:string
-property_value: DiffMono "146.057909" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-xref: GNO:G02438LG
-is_a: MOD:00693
-
-[Term]
-id: MOD:00737
-name: N-acetylneuraminylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of an amino acid residue or of a modifying group with an N-acetylneuraminic acid (sialic acid) group through a glycosidic bond." [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 291
-synonym: "N-acetylneuraminic acid (Sialic acid, NeuAc, NANA, SA)" EXACT DeltaMass-label []
-synonym: "NeuNAc" EXACT PSI-MOD-label []
-property_value: DiffAvg "291.26" xsd:float
-property_value: DiffFormula "C 11 H 17 N 1 O 8" xsd:string
-property_value: DiffMono "291.095417" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-xref: GNO:G76685HR
-is_a: MOD:00693
-
-[Term]
-id: MOD:00738
-name: iron containing modified residue
-def: "A protein modification that effectively substitutes an iron atom or a cluster containing iron for hydrogen atoms, or that coordinates an iron ion." [PubMed:18688235]
-synonym: "FeRes" EXACT PSI-MOD-label []
-is_a: MOD:00698
-
-[Term]
-id: MOD:00739
-name: iron-sulfur cluster containing modification
-def: "A protein modification that effectively substitutes a cluster of iron and sulfur atoms for hydrogen atoms." [PubMed:18688235]
-synonym: "FeSRes" EXACT PSI-MOD-label []
-is_a: MOD:00738
-is_a: MOD:00860
-
-[Term]
-id: MOD:00740
-name: manganese containing modified residue
-def: "A protein modification that effectively substitutes a manganese atom or a cluster containing manganese for hydrogen atoms, or that coordinates a manganese ion." [PubMed:18688235]
-synonym: "MnRes" EXACT PSI-MOD-label []
-is_a: MOD:00698
-
-[Term]
-id: MOD:00741
-name: nickel containing modified residue
-def: "A protein modification that effectively substitutes a nickel atom or a cluster containing nickel for hydrogen atoms, or that coordinates a nickel ion." [PubMed:18688235]
-synonym: "NiRes" EXACT PSI-MOD-label []
-is_a: MOD:00698
-
-[Term]
-id: MOD:00742
-name: copper containing modified residue
-def: "A protein modification that effectively substitutes a copper atom or a cluster containing copper for hydrogen atoms, or that coordinates a copper ion." [PubMed:18688235]
-synonym: "CuRes" EXACT PSI-MOD-label []
-is_a: MOD:00698
-
-[Term]
-id: MOD:00743
-name: molybdenum containing modified residue
-def: "A protein modification that effectively substitutes a molybdenum atom or a cluster containing molybdenum for hydrogen atoms, or that coordinates a molybdenum ion." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "MoRes" EXACT PSI-MOD-label []
-is_a: MOD:00698
-
-[Term]
-id: MOD:00744
-name: molybdenum pterin containing modification
-def: "A protein modification containing a molybdenum atom in a pterin ring system." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "MoPterRes" EXACT PSI-MOD-label []
-is_a: MOD:00743
-is_a: MOD:00748
-
-[Term]
-id: MOD:00745
-name: selenium containing residue
-def: "A protein modification that effectively substitutes a selenium atom or a cluster containing selenium for hydrogen atoms." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "SeRes" EXACT PSI-MOD-label []
-is_a: MOD:01156
-
-[Term]
-id: MOD:00746
-name: tungsten containing modified residue
-def: "A protein modification that effectively substitutes a tungsten atom or a cluster containing tungsten for hydrogen atoms, or that coordinates a tungsten ion." [PubMed:18688235]
-synonym: "WRes" EXACT PSI-MOD-label []
-is_a: MOD:00698
-
-[Term]
-id: MOD:00747
-name: sodium containing modified residue
-def: "A protein modification that effectively substitutes a sodium atom for a hydrogen atom." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "NaRes" EXACT PSI-MOD-label []
-is_a: MOD:00698
-
-[Term]
-id: MOD:00748
-name: pterin modified residue
-def: "A protein modification that effectively results from forming an adduct with a compound containing a pterin group." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "PterRes" EXACT PSI-MOD-label []
-is_a: MOD:01156
-
-[Term]
-id: MOD:00749
-name: sulfur substitution for oxygen
-def: "A protein modification that effectively substitutes a sulfur atom for an oxygen atom." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "S(O)Res" EXACT PSI-MOD-label []
-is_a: MOD:00860
-
-[Term]
-id: MOD:00750
-name: deoxyribonucleic acid linked residue
-def: "A protein modification that effectively crosslinks an amino acid residue and the 3'- or 5'-end of DNA through a phosphodiester bond." [PubMed:18688235]
-synonym: "DNARes" EXACT PSI-MOD-label []
-is_a: MOD:00701
-
-[Term]
-id: MOD:00751
-name: ribonucleic acid linked residue
-def: "a protein modification" [PubMed:18688235]
-synonym: "RNARes" EXACT PSI-MOD-label []
-is_a: MOD:00701
-
-[Term]
-id: MOD:00752
-name: monoadenosine diphosphoribosyl (ADP-ribosyl) modified residue
-def: "A protein modification that effectively results from forming an adduct with one ADP-ribose through formation of a glycosidic bond." [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 541.
-subset: PSI-MOD-slim
-synonym: "ADP-rybosylation (from NAD)" EXACT DeltaMass-label []
-synonym: "ADPRib1Res" EXACT PSI-MOD-label []
-property_value: DiffAvg "541.30" xsd:float
-property_value: DiffFormula "C 15 H 21 N 5 O 13 P 2" xsd:string
-property_value: DiffMono "541.061109" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:02087
-
-[Term]
-id: MOD:00753
-name: chlorinated residue
-def: "A protein modification that effectively substitutes a chlorine atom for a hydrogen atom." [PubMed:18688235]
-synonym: "ClRes" EXACT PSI-MOD-label []
-property_value: Origin "X" xsd:string
-is_a: MOD:00694
-
-[Term]
-id: MOD:00754
-name: brominated residue
-def: "A protein modification that effectively substitutes a bromine atom for a hydrogen atom." [PubMed:18688235]
-synonym: "BrRes" EXACT PSI-MOD-label []
-property_value: Origin "X" xsd:string
-is_a: MOD:00694
-
-[Term]
-id: MOD:00755
-name: iodinated residue
-def: "A protein modification that effectively substitutes an iodine atom of a residue for a hydrogen atom." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "IRes" EXACT PSI-MOD-label []
-property_value: Origin "X" xsd:string
-is_a: MOD:00694
-
-[Term]
-id: MOD:00756
-name: 4-hydroxy-D-valine
-def: "A protein modification that effectively converts an L-valine residue to 4-hydroxy-D-valine." [PubMed:15853325, RESID:AA0388]
-synonym: "(2R,3Xi)-2-amino-4-hydroxy-3-methylbutanoic acid" EXACT RESID-systematic []
-synonym: "4-hydroxy-D-valine" EXACT RESID-name []
-synonym: "D-4HyVal" EXACT PSI-MOD-label []
-synonym: "D-gamma-hydroxyvaline" EXACT RESID-alternate []
-synonym: "MOD_RES D-4-hydroxyvaline" EXACT UniProt-feature []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 5 H 9 N 1 O 2" xsd:string
-property_value: MassAvg "115.13" xsd:float
-property_value: MassMono "115.063329" xsd:float
-property_value: Origin "V" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0111
-is_a: MOD:00425
-is_a: MOD:00664
-
-[Term]
-id: MOD:00757
-name: O4-galactosyl-L-hydroxyproline
-def: "A protein modification that effectively converts an L-proline residue to O4-galactosyl-L-hydroxyproline." [RESID:AA0389]
-comment: secondary to RESID:AA0030
-synonym: "(2S,4R)-4-(beta-D-galactopyranosyloxy)pyrrolidine-2-carboxylic acid" EXACT RESID-systematic []
-synonym: "4-(beta-D-galactopyranosyloxy)proline" EXACT RESID-alternate []
-synonym: "4-(galactosyloxy)proline" EXACT RESID-alternate []
-synonym: "beta-galactopyranosyl-4-hydroxyproline" EXACT RESID-alternate []
-synonym: "O4-galactosyl-L-hydroxyproline" EXACT RESID-name []
-synonym: "O4-glycosyl-hydroxyproline" EXACT RESID-alternate []
-synonym: "CARBOHYD O-linked (Gal) hydroxyproline" EXACT UniProt-feature []
-property_value: DiffAvg "178.14" xsd:float
-property_value: DiffFormula "C 6 H 10 N 0 O 6" xsd:string
-property_value: DiffMono "178.047738" xsd:float
-property_value: Formula "C 11 H 17 N 1 O 7" xsd:string
-property_value: MassAvg "275.26" xsd:float
-property_value: MassMono "275.100502" xsd:float
-property_value: Origin "P" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0558
-is_a: MOD:00915
-
-[Term]
-id: MOD:00758
-name: O4-(N-acetylamino)glucosyl-L-hydroxyproline
-def: "A protein modification that effectively converts an L-proline residue to O4-(N-acetylamino)glucosyl-L-hydroxyproline." [PubMed:15238247, PubMed:9660787, RESID:AA0390]
-comment: secondary to RESID:AA0030
-synonym: "(2S,4R)-4-[2-acetamido-2-deoxy-alpha-D-glucopyranosyloxy]pyrrolidine-2-carboxylic acid" EXACT RESID-systematic []
-synonym: "4-(N-acetylglucosaminyloxy)proline" EXACT RESID-alternate []
-synonym: "4-[(2-N-acetylamino)-alpha-D-glucopyranosyl]oxyproline" EXACT RESID-alternate []
-synonym: "alpha-2-(N-acetylamino)glucopyranosyl-4-hydroxyproline" EXACT RESID-alternate []
-synonym: "HexNAc" RELATED PSI-MS-label []
-synonym: "O4-(N-acetylamino)glucosyl-L-hydroxyproline" EXACT RESID-name []
-synonym: "O4-glycosyl-hydroxyproline" EXACT RESID-alternate []
-synonym: "O4GlcNAcHyPro" EXACT PSI-MOD-label []
-synonym: "CARBOHYD O-linked (GlcNAc) hydroxyproline" EXACT UniProt-feature []
-property_value: DiffAvg "219.19" xsd:float
-property_value: DiffFormula "C 8 H 13 N 1 O 6" xsd:string
-property_value: DiffMono "219.074287" xsd:float
-property_value: Formula "C 13 H 20 N 2 O 7" xsd:string
-property_value: MassAvg "316.31" xsd:float
-property_value: MassMono "316.127051" xsd:float
-property_value: Origin "P" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0578
-is_a: MOD:01677
-
-[Term]
-id: MOD:00759
-name: fucosylated biantennary (-1 galactose) N4-glycosylated asparagine
-def: "modification from Unimod N-linked glycosylation" [Unimod:307]
-synonym: "dHex(1)Hex(4)HexNAc(4)" RELATED PSI-MS-label []
-synonym: "Fucosylated biantennary (-1 galactose)" RELATED Unimod-description []
-property_value: DiffAvg "1607.48" xsd:float
-property_value: DiffFormula "C 62 H 102 N 4 O 44" xsd:string
-property_value: DiffMono "1606.586693" xsd:float
-property_value: Formula "C 66 H 108 N 6 O 46" xsd:string
-property_value: MassAvg "1721.59" xsd:float
-property_value: MassMono "1720.629620" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:307
-xref: GNO:G59937CP
-is_a: MOD:00725
-is_a: MOD:00160
-
-[Term]
-id: MOD:00760
-name: biantennary N4-glycosylated asparagine
-def: "modification from Unimod N-linked glycosylation - missing ref" [Unimod:311]
-synonym: "Biantennary" RELATED Unimod-description []
-synonym: "Hex(5)HexNAc(4)" RELATED PSI-MS-label []
-property_value: DiffAvg "1623.48" xsd:float
-property_value: DiffFormula "C 62 H 102 N 4 O 45" xsd:string
-property_value: DiffMono "1622.581607" xsd:float
-property_value: Formula "C 66 H 108 N 6 O 47" xsd:string
-property_value: MassAvg "1737.59" xsd:float
-property_value: MassMono "1736.624535" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:311
-xref: GNO:G10486CT
-is_a: MOD:00725
-is_a: MOD:00160
-
-[Term]
-id: MOD:00761
-name: monohexosylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of an amino acid residue or of a modifying group with one hexose sugar group through a glycosidic bond." [PubMed:18688235]
-synonym: "Hex1" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "162.14" xsd:float
-property_value: DiffFormula "C 6 H 10 O 5" xsd:string
-property_value: DiffMono "162.052823" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-xref: GNO:G81399MY
-is_a: MOD:00434
-
-[Term]
-id: MOD:00762
-name: biantennary (-2 galactose) N4-glycosylated asparagine
-def: "modification from Unimod N-linked glycosylation - missing ref" [Unimod:309]
-synonym: "Biantennary (-2 galactose)" RELATED Unimod-description []
-synonym: "Hex(3)HexNAc(4)" RELATED PSI-MS-label []
-property_value: DiffAvg "1299.20" xsd:float
-property_value: DiffFormula "C 50 H 82 N 4 O 35" xsd:string
-property_value: DiffMono "1298.475960" xsd:float
-property_value: Formula "C 54 H 88 N 6 O 37" xsd:string
-property_value: MassAvg "1413.30" xsd:float
-property_value: MassMono "1412.518888" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:309
-xref: GNO:G35029YA
-is_a: MOD:00725
-is_a: MOD:00160
-
-[Term]
-id: MOD:00763
-name: biantennary (-1 galactose) N4-glycosylated asparagine
-def: "modification from Unimod N-linked glycosylation - missing ref" [Unimod:310]
-synonym: "Biantennary (-1 galactose)" RELATED Unimod-description []
-synonym: "Hex(4)HexNAc(4)" RELATED PSI-MS-label []
-property_value: DiffAvg "1461.34" xsd:float
-property_value: DiffFormula "C 56 H 92 N 4 O 40" xsd:string
-property_value: DiffMono "1460.528784" xsd:float
-property_value: Formula "C 60 H 98 N 6 O 42" xsd:string
-property_value: MassAvg "1575.44" xsd:float
-property_value: MassMono "1574.571711" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:310
-xref: GNO:G72787SB
-is_a: MOD:00725
-is_a: MOD:00160
-
-[Term]
-id: MOD:00764
-name: glycoconjugated residue
-def: "A protein modification that effectively results from forming an adduct with a carbohydrate-like group either through enzymatic formation of a glycosidic bond, or through non-enzymatic glycation formation of a Schiff-base or an Amadori ketosamine residue adduct." [PubMed:18688235, PubMed:3743566]
-subset: PSI-MOD-slim
-is_a: MOD:01156
-
-[Term]
-id: MOD:00765
-name: cysteinylation (disulfide with free L-cysteine)
-def: "A protein modification that effectively converts an L-cysteine residue to S-(L-cysteinyl)-L-cysteine, forming a disulfide bond with free cysteine." [DeltaMass:260, PubMed:1988019, PubMed:2001356, PubMed:2076469, PubMed:3083866, PubMed:366603, PubMed:7918467, PubMed:8344916, RESID:AA0025#CYS1, Unimod:312]
-comment: This entry is for formation of a disulfide bond between a peptide cysteine and a free cysteine. For the cystine cross-link, see MOD:00234. From DeltaMass: (name misspelled and formula incorrect, N and O reversed) Formula: C6H10O2N3S2 Monoisotopic Mass Change: 222.013 Average Mass Change: 222.283
-subset: PSI-MOD-slim
-synonym: "(2R,2'R)-3,3'-disulfane-1,2-diylbis(2-aminopropanoic acid)" EXACT RESID-systematic []
-synonym: "2-amino-3-(2-amino-2-carboxy-ethyl)disulfanyl-propanoic acid" RELATED RESID-misnomer []
-synonym: "3,3'-disulfane-1,2-diylbis(2-azanylpropanoic acid)" EXACT RESID-alternate []
-synonym: "3,3'-dithiobis(2-aminopropanoic acid)" EXACT RESID-alternate []
-synonym: "3,3'-dithiobisalanine" EXACT RESID-alternate []
-synonym: "3,3'-dithiodialanine" EXACT RESID-alternate []
-synonym: "beta,beta'-diamino-beta,beta'-dicarboxydiethyldisulfide" EXACT RESID-alternate []
-synonym: "beta,beta'-dithiodialanine" EXACT RESID-alternate []
-synonym: "bis(alpha-aminopropionic acid)-beta-disulfide" EXACT RESID-alternate []
-synonym: "bis(beta-amino-beta-carboxyethyl)disulfide" EXACT RESID-alternate []
-synonym: "Cysteinylation" EXACT DeltaMass-label []
-synonym: "dicysteine" EXACT RESID-alternate []
-synonym: "L-cystine" EXACT RESID-name []
-synonym: "MOD_RES S-cysteinyl cysteine" EXACT UniProt-feature []
-synonym: "S-cystenyl cystenyl" EXACT DeltaMass-label []
-synonym: "SCysCys" EXACT PSI-MOD-label []
-property_value: DiffAvg "119.14" xsd:float
-property_value: DiffFormula "C 3 H 5 N 1 O 2 S 1" xsd:string
-property_value: DiffMono "119.004099" xsd:float
-property_value: Formula "C 6 H 10 N 2 O 3 S 2" xsd:string
-property_value: MassAvg "222.28" xsd:float
-property_value: MassMono "222.013284" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:312
-xref: uniprot.ptm:PTM-0415
-is_a: MOD:00905
-is_a: MOD:01862
-
-[Term]
-id: MOD:00766
-name: C terminal -K from HC of MAb
-def: "modification from Unimod Post-translational - C-terminal loss of lysine OBSOLETE because the idenical to MOD:01642. Remap to MOD:01642" [PubMed:16078144, Unimod:313]
-synonym: "Loss of C-terminal K from Heavy Chain of MAb" RELATED Unimod-description []
-synonym: "Lys-loss" RELATED PSI-MS-label []
-property_value: DiffAvg "-128.18" xsd:float
-property_value: DiffFormula "C -6 H -12 N -2 O -1" xsd:string
-property_value: DiffMono "-128.094963" xsd:float
-property_value: Origin "X" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: Unimod:313
-replaced_by: MOD:01642
-is_obsolete: true
-
-[Term]
-id: MOD:00767
-name: glycated residue
-def: "A modification produced in a non-enzymatic reaction between a carbohydrate carbonyl group (C1 of aldohexose or C2 of fructose) and a protein amino group to form a Schiff-base or an Amadori ketosamine residue adduct." [PubMed:18688235]
-property_value: Source "artifact" xsd:string
-is_a: MOD:00764
-
-[Term]
-id: MOD:00768
-name: methionine oxidation with neutral loss of 80 Da
-def: "Oxidation of methionine to methionine sulfone with neutral loss of CH3SO2H." [PubMed:18688235, PubMed:9004526]
-comment: Originally created from Unimod:508 that was later deleted.
-property_value: DiffAvg "-80.10" xsd:float
-property_value: DiffFormula "C -1 H -4 N 0 O -2 S -1" xsd:string
-property_value: DiffMono "-79.993200" xsd:float
-property_value: Formula "C 4 H 5 N 1 O 1 S 0" xsd:string
-property_value: MassAvg "83.09" xsd:float
-property_value: MassMono "83.037114" xsd:float
-property_value: Origin "M" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00431
-
-[Term]
-id: MOD:00769
-name: residues isobaric at 71.0-71.1 Da
-def: "Natural or modified residues with a mass of 71.0-71.1 Da." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:00616
-
-[Term]
-id: MOD:00770
-name: residues isobaric at a resolution below 0.01 Da
-def: "Natural or modified residues that are isobaric at a resolution below 0.01 Da." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:00616
-
-[Term]
-id: MOD:00771
-name: residues isobaric at 166.98-167.00 Da
-def: "Natural or modified residues with a mass of 166.98-167.00 Da." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:00770
-
-[Term]
-id: MOD:00772
-name: vanadium containing modified residue
-def: "A protein modification that effectively substitutes a vanadium atom or a cluster containing vanadium for hydrogen atoms, or that coordinates a vanadium ion." [PubMed:18688235]
-synonym: "VRes" EXACT PSI-MOD-label []
-is_a: MOD:00698
-
-[Term]
-id: MOD:00773
-name: residues isobaric at 181.00-181.02 Da
-def: "Natural or modified residues with a mass of 181.00-181.02 Da." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:00770
-
-[Term]
-id: MOD:00774
-name: residues isobaric at 243.02-243.03 Da
-def: "Natural or modified residues with a mass of 243.02-243.03 Da." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:00770
-
-[Term]
-id: MOD:00775
-name: L-asparagine (His)
-def: "An artifactual protein modification that converts an L-histidine residue to L-asparagine by oxidative degradation." [OMSSA:54, PubMed:9252331, Unimod:348]
-synonym: "His->Asn" RELATED PSI-MS-label []
-synonym: "his2asnh" EXACT OMSSA-label []
-synonym: "histidine oxidation to aspargine" RELATED Unimod-description []
-property_value: DiffAvg "-23.04" xsd:float
-property_value: DiffFormula "C -2 H -1 N -1 O 1" xsd:string
-property_value: DiffMono "-23.015984" xsd:float
-property_value: Formula "C 4 H 6 N 2 O 2" xsd:string
-property_value: MassAvg "114.10" xsd:float
-property_value: MassMono "114.042927" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:348
-is_a: MOD:00909
-is_a: MOD:02088
-
-[Term]
-id: MOD:00776
-name: L-aspartic acid (His)
-def: "An artifactual protein modification that converts an L-histidine residue to L-aspartic acid by oxidative degradation." [OMSSA:55, PubMed:9252331, Unimod:349]
-comment: From OMSSA: desc=\"oxidation of H to D\" monomass= -23.015984 (this is the same mass difference as OMSSA:54, his2asnh) [JSG].
-synonym: "His->Asp" RELATED PSI-MS-label []
-synonym: "his2asph" EXACT OMSSA-label []
-synonym: "histidine oxidation to aspartic acid" RELATED Unimod-description []
-property_value: DiffAvg "-22.05" xsd:float
-property_value: DiffFormula "C -2 H -2 N -2 O 2" xsd:string
-property_value: DiffMono "-22.031969" xsd:float
-property_value: Formula "C 4 H 5 N 1 O 3" xsd:string
-property_value: MassAvg "115.09" xsd:float
-property_value: MassMono "115.026943" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:349
-is_a: MOD:00909
-is_a: MOD:02088
-
-[Term]
-id: MOD:00777
-name: residues isobaric at 182.96-182.98 Da
-def: "Natural or modified residues with a mass of 182.96-182.98 Da." [PubMed:18688235]
-is_a: MOD:00770
-is_a: MOD:00778
-
-[Term]
-id: MOD:00778
-name: residues isobaric at 182.9-183.0 Da
-def: "Natural or modified residues with a mass of 182.9-183.0 Da." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:00616
-
-[Term]
-id: MOD:00779
-name: lysine oxidation to aminoadipic semialdehyde
-def: "OBSOLETE because redundant with MOD:00130. Remap to MOD:00130." [DeltaMass:352, PubMed:11332453, PubMed:358196, PubMed:5337886, PubMed:5529814, Unimod:352]
-comment: From DeltaMass: Average Mass: -1 Average Mass Change:-1 References:Amici A, Levine, RL, Tsai, L, and Stadtman, ER: Conversion of amino acid residues in proteins and amino acid homopolymers to carbonyl derivatives by metal-catalyzed oxidation reactions. Journal of Biological Chemistry 264: 3341-3346 1989.Requena JR, Chao CC, Levine RL, and Stadtman ER: Glutamic and aminoadipic semialdehydes are the main carbonyl products of metal-catalyzed oxidation of proteins. Proceedings of the National Academy of Sciences USA 98: 69-74 2001.
-synonym: "Oxidation of lysine (to aminoadipic semialdehyde)" EXACT DeltaMass-label []
-property_value: DiffAvg "-1.03" xsd:float
-property_value: DiffFormula "H -3 N -1 O 1" xsd:string
-property_value: DiffMono "-1.031634" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-replaced_by: MOD:00130
-xref: Unimod:352
-is_obsolete: true
-
-[Term]
-id: MOD:00780
-name: N-acetyl-L-asparagine
-def: "A protein modification that effectively converts an L-asparagine residue to N-acetyl-L-asparagine." [PubMed:18688235]
-comment: This modification has not been observed to occur naturally.
-synonym: "AcAsn" EXACT PSI-MOD-label []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 2 H 2 N 0 O 1" xsd:string
-property_value: DiffMono "42.010565" xsd:float
-property_value: Formula "C 6 H 8 N 2 O 3" xsd:string
-property_value: MassAvg "156.14" xsd:float
-property_value: MassMono "156.053492" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00903
-is_a: MOD:01458
-
-[Term]
-id: MOD:00781
-name: N2-acetyl-L-histidine
-def: "A protein modification that effectively converts an L-histidine residue to N2-acetyl-L-histidine." [PubMed:18688235]
-comment: This modification has not been observed to occur naturally.
-synonym: "AcHis" EXACT PSI-MOD-label []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 2 H 2 N 0 O 1" xsd:string
-property_value: DiffMono "42.010565" xsd:float
-property_value: Formula "C 8 H 9 N 3 O 2" xsd:string
-property_value: MassAvg "179.18" xsd:float
-property_value: MassMono "179.069477" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00909
-is_a: MOD:01458
-
-[Term]
-id: MOD:00782
-name: N-acetyl-L-leucine
-def: "A protein modification that effectively converts an L-leucine residue to N-acetyl-L-leucine." [PubMed:18688235]
-comment: This modification has not been observed to occur naturally.
-synonym: "AcLeu" EXACT PSI-MOD-label []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 2 H 2 N 0 O 1" xsd:string
-property_value: DiffMono "42.010565" xsd:float
-property_value: Formula "C 8 H 14 N 1 O 2" xsd:string
-property_value: MassAvg "156.20" xsd:float
-property_value: MassMono "156.102454" xsd:float
-property_value: Origin "L" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00911
-is_a: MOD:01458
-
-[Term]
-id: MOD:00783
-name: dimethylated L-arginine
-def: "A protein modification that effectively replaces two hydrogen atoms of an L-arginine residue with two methyl groups." [OMSSA:37, Unimod:36#R]
-subset: PSI-MOD-slim
-synonym: "Dimethyl" RELATED PSI-MS-label []
-synonym: "dimethylr" EXACT OMSSA-label []
-synonym: "NNMe2Arg" EXACT PSI-MOD-label []
-property_value: DiffAvg "28.05" xsd:float
-property_value: DiffFormula "C 2 H 4 N 0 O 0" xsd:string
-property_value: DiffMono "28.031300" xsd:float
-property_value: Formula "C 8 H 16 N 4 O 1" xsd:string
-property_value: MassAvg "184.24" xsd:float
-property_value: MassMono "184.132411" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:36
-xref: uniprot.ptm:PTM-0341
-is_a: MOD:00429
-is_a: MOD:00658
-
-[Term]
-id: MOD:00784
-name: N-acetyl-L-phenylalanine
-def: "A protein modification that effectively converts an L-phenylalanine residue to N-acetyl-L-phenylalanine." [PubMed:18688235]
-comment: This modification has not been observed to occur naturally.
-synonym: "AcPhe" EXACT PSI-MOD-label []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 2 H 2 N 0 O 1" xsd:string
-property_value: DiffMono "42.010565" xsd:float
-property_value: Formula "C 11 H 11 N 1 O 2" xsd:string
-property_value: MassAvg "189.21" xsd:float
-property_value: MassMono "189.078979" xsd:float
-property_value: Origin "F" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00914
-is_a: MOD:01458
-
-[Term]
-id: MOD:00785
-name: N2-acetyl-L-tryptophan
-def: "A protein modification that effectively converts an L-tryptophan residue to N2-acetyl-L-tryptophan." [PubMed:18688235]
-comment: This modification has not been observed to occur naturally.
-synonym: "AcTrp" EXACT PSI-MOD-label []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 2 H 2 N 0 O 1" xsd:string
-property_value: DiffMono "42.010565" xsd:float
-property_value: Formula "C 13 H 12 N 2 O 2" xsd:string
-property_value: MassAvg "228.25" xsd:float
-property_value: MassMono "228.089878" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00918
-is_a: MOD:01458
-
-[Term]
-id: MOD:00786
-name: deuterium substituted residue
-def: "A protein modification that effectively substitutes one or more (2)H deuterium atoms for (1)H protium atoms." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "D(H)Res" EXACT PSI-MOD-label []
-is_a: MOD:00839
-
-[Term]
-id: MOD:00787
-name: diisopropylphosphoserine
-def: "modification from Unimod - label for the active site serine of the serine esterase/protease family also shown to label tyrosine in serum albumin" [Unimod:362]
-synonym: "Diisopropylphosphate" RELATED Unimod-interim []
-synonym: "O-Diisopropylphosphorylation" RELATED Unimod-description []
-property_value: DiffAvg "164.14" xsd:float
-property_value: DiffFormula "C 6 H 13 O 3 P 1" xsd:string
-property_value: DiffMono "164.060231" xsd:float
-property_value: Formula "C 9 H 18 N 1 O 5 P 1" xsd:string
-property_value: MassAvg "251.22" xsd:float
-property_value: MassMono "251.092259" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:362
-is_a: MOD:00848
-is_a: MOD:00861
-is_a: MOD:00916
-
-[Term]
-id: MOD:00788
-name: isopropylphosphotyrosine
-def: "modification from Unimod" [Unimod:363]
-synonym: "Isopropylphospho" RELATED Unimod-interim []
-synonym: "O-Isopropylphosphorylation" RELATED Unimod-description []
-property_value: DiffAvg "122.06" xsd:float
-property_value: DiffFormula "C 3 H 7 O 3 P 1" xsd:string
-property_value: DiffMono "122.013281" xsd:float
-property_value: Formula "C 12 H 16 N 1 O 5 P 1" xsd:string
-property_value: MassAvg "285.24" xsd:float
-property_value: MassMono "285.076609" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:363
-is_a: MOD:00848
-is_a: MOD:00861
-is_a: MOD:00919
-
-[Term]
-id: MOD:00789
-name: Bruker Daltonics SERVA-ICPL(TM) quantification chemistry, heavy form
-def: "modification from Unimod - isotopic label ICPL method - The paper describes an H/D labeling strategy whereas the commercial product follows a C/13C labeling strategy. The digest is typically applied AFTER ICPL_light/heavy labeling, only Protein N-term labeling and Lys-specific labeling is applied." [PubMed:15602776, Unimod:364, URL:http\://www.serva.de/products/sheets/39230-E.pdf]
-synonym: "Bruker Daltonics SERVA-ICPL(TM) quantification chemistry, heavy form" RELATED Unimod-description []
-synonym: "ICPL:13C(6)" RELATED PSI-MS-label []
-property_value: DiffAvg "111.04" xsd:float
-property_value: DiffFormula "(13)C 6 H 3 N 1 O 1" xsd:string
-property_value: DiffMono "111.041593" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:364
-is_a: MOD:01428
-
-[Term]
-id: MOD:00790
-name: Bruker Daltonics SERVA-ICPL(TM) quantification chemistry, light form
-def: "modification from Unimod - isotopic label ICPL method - The paper describes an H/D labeling strategy whereas the commercial product follows a C/13C labeling strategy. The digest is typically applied AFTER ICPL_light/heavy labeling, only Protein N-term labeling and Lys-specific labeling is applied." [PubMed:15602776, Unimod:365, URL:http\://www.serva.de/products/sheets/39230-E.pdf]
-synonym: "Bruker Daltonics SERVA-ICPL(TM) quantification chemistry, light form" RELATED Unimod-description []
-synonym: "ICPL" RELATED PSI-MS-label []
-property_value: DiffAvg "105.02" xsd:float
-property_value: DiffFormula "(12)C 6 H 3 N 1 O 1" xsd:string
-property_value: DiffMono "105.021464" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:365
-is_a: MOD:01426
-
-[Term]
-id: MOD:00791
-name: 1x(18)O labeled deamidated L-glutamine
-def: "A protein modification that effectively converts an L-glutamine residue to L-glutamic acid with one (18)O." [PubMed:8382902, Unimod:366#Q]
-subset: PSI-MOD-slim
-synonym: "Deamidated:18O(1)" RELATED PSI-MS-label []
-synonym: "Deamidation in presence of O18" RELATED Unimod-description []
-property_value: DiffAvg "2.99" xsd:float
-property_value: DiffFormula "H -1 N -1 (18)O 1" xsd:string
-property_value: DiffMono "2.988262" xsd:float
-property_value: Formula "C 5 H 7 N 1 (16)O 2 (18)O 1" xsd:string
-property_value: MassAvg "131.05" xsd:float
-property_value: MassMono "131.046839" xsd:float
-property_value: Origin "Q" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:366
-relationship: derives_from MOD:00685
-is_a: MOD:00852
-
-[Term]
-id: MOD:00792
-name: deuterium monosubstituted residue
-def: "A protein modification that effectively substitutes one (2)H deuterium atom for one (1)H protium atom." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "D(H)1Res" EXACT PSI-MOD-label []
-is_a: MOD:00786
-
-[Term]
-id: MOD:00793
-name: dehydroalanine (Cys)
-def: "A protein modification that effectively converts an L-cysteine residue to dehydroalanine." [ChEBI:17123, DeltaMass:8, PubMed:10220322, PubMed:11212008, PubMed:1547888, PubMed:15799070, PubMed:1815586, PubMed:20805503, PubMed:2914619, PubMed:7947813, PubMed:8239649, RESID:AA0181#CYS, Unimod:368]
-comment: From DeltaMass: In an attempt to clarfiy the difference between the modification of cysteine to lanthionine and cysteine to dehydroalanine, the following contributions from the ABRF email forum are presented:Structurally speaking lanthionine is like cystine but lacks one S atom. I imagine one can think of it as a condensation of cysteine and dehydroalanine but I do not know how it is made biologically. Dehydroalanine could be derived from either serine or cysteine. If I recall Biochem 101 correctly lanthionine was first found in wool.-Lowell Ericsson (ERICSSONLH@U.WASHINGTON.EDU)As far as I know, the structure of lanthionine is two Ala's joined by a single sulphur with the loss of two hydrogens from the methyl group of the Ala.Stephen Bayne (sbay@novo.dk)Regarding the structure of lanthionine and dehydroalanine: dehydroalanine is formed by the loss of one sulfur atom and two hydrogen atoms from ONE cysteine residue. lanthionine is formed from TWO cysteines, is a thioether, and contains one sulfur atom less than the amino acid cystine. Dan McCormick (MCCORMICK@rcf.mayo.edu) [DeltaMass]. Most bacterially produced lanthionine crosslinks are made by dehydration of L-serine to dehydroalanine, and then reaction with L-cysteine so as to produce chiral inversion at the alpha-carbon of the original L-serine; the lanthionine is a meso-diastereomer with L-configuration of the original cysteine alpha-carbon and D-configuration of the original L-serine alpha-carbon. In cypemycin dehydroalanine has been shown to be produced by loss of hydrogen sulfide from cysteine. Beta-elimination of hydrogen sulfide does occur during treatment with performic acid [JSG].
-subset: PSI-MOD-slim
-synonym: "2,3-didehydroalanine" EXACT RESID-alternate []
-synonym: "2-aminoacrylic acid" EXACT RESID-alternate []
-synonym: "2-aminopropenoic acid" EXACT RESID-systematic []
-synonym: "4-methylidene-imidazole-5-one (MIO) active site" EXACT RESID-alternate []
-synonym: "anhydroserine" EXACT RESID-alternate []
-synonym: "Cys->Dha" RELATED PSI-MS-label []
-synonym: "dehydroalanine" EXACT RESID-name []
-synonym: "Dehydroalanine (from Cysteine)" EXACT DeltaMass-label []
-synonym: "Dehydroalanine (from Cysteine)" RELATED Unimod-description []
-synonym: "Dha" EXACT RESID-alternate []
-synonym: "dHAla(Cys)" EXACT PSI-MOD-label []
-synonym: "MOD_RES 2,3-didehydroalanine (Cys)" EXACT UniProt-feature []
-property_value: DiffAvg "-34.08" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0 S -1" xsd:string
-property_value: DiffMono "-33.987721" xsd:float
-property_value: Formula "C 3 H 3 N 1 O 1" xsd:string
-property_value: MassAvg "69.06" xsd:float
-property_value: MassMono "69.021464" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:368
-xref: uniprot.ptm:PTM-0468
-is_a: MOD:00905
-is_a: MOD:01168
-
-[Term]
-id: MOD:00794
-name: pyrrolidone from proline
-def: "OBSOLETE because redundant and identical to MOD:00477. Remap to MOD:00477." [PubMed:9252331, Unimod:369]
-comment: This Unimod entry appears to have come from the same description in PubMed:9252331 as Unimod:360. This entry was not annotated as being approved. Neither difference formula corresponds to the result described in the original citation PubMed:2161657.
-synonym: "Pro->Pyrrolidone" RELATED Unimod-interim []
-synonym: "Pyrrolidone from Proline" RELATED Unimod-description []
-property_value: DiffAvg "-28.01" xsd:float
-property_value: DiffFormula "C -1 O -1" xsd:string
-property_value: DiffMono "-27.994915" xsd:float
-property_value: Formula "C 4 H 7 N 1 O 0" xsd:string
-property_value: MassAvg "69.11" xsd:float
-property_value: MassMono "69.057849" xsd:float
-property_value: Origin "P" xsd:string
-property_value: Source "artifact" xsd:string
-replaced_by: MOD:00477
-xref: Unimod:369
-is_obsolete: true
-
-[Term]
-id: MOD:00795
-name: Michael addition of hydroxymethylvinyl ketone to cysteine
-def: "modification from Unimod" [PubMed:11743741, Unimod:371]
-synonym: "HMVK" RELATED PSI-MS-label []
-synonym: "Michael addition of hydroxymethylvinyl ketone to cysteine" RELATED Unimod-description []
-property_value: DiffAvg "86.09" xsd:float
-property_value: DiffFormula "C 4 H 6 O 2" xsd:string
-property_value: DiffMono "86.036779" xsd:float
-property_value: Formula "C 7 H 11 N 1 O 3 S 1" xsd:string
-property_value: MassAvg "189.23" xsd:float
-property_value: MassMono "189.045964" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:371
-is_a: MOD:00905
-
-[Term]
-id: MOD:00796
-name: L-ornithine (Arg)
-def: "A protein modification that effectively converts an L-arginine residue to L-ornithine." [DeltaMass:129, OMSSA:163, PubMed:15489230, Unimod:372]
-subset: PSI-MOD-slim
-synonym: "Arg->Orn" RELATED PSI-MS-label []
-synonym: "arg2orn" EXACT OMSSA-label []
-synonym: "Ornithine (from Arginine)" EXACT DeltaMass-label []
-synonym: "Ornithine from Arginine" RELATED Unimod-description []
-synonym: "Ornithyl" EXACT DeltaMass-label []
-property_value: DiffAvg "-42.04" xsd:float
-property_value: DiffFormula "C -1 H -2 N -2" xsd:string
-property_value: DiffMono "-42.021798" xsd:float
-property_value: Formula "C 5 H 10 N 2 O 1" xsd:string
-property_value: MassAvg "114.15" xsd:float
-property_value: MassMono "114.079313" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:372
-is_a: MOD:00902
-
-[Term]
-id: MOD:00797
-name: 2-(S-L-cysteinyl)pyruvic acid O-phosphothioketal
-def: "a protein modification that effectively converts an L-cysteine residue to the PEP adduct, 2-(S-L-cysteinyl)pyruvic acid O-phosphothioketal" [PubMed:4696757, PubMed:7999765, PubMed:8664284, RESID:AA0391, ChEBI:149496]
-synonym: "(2R)-2-amino-3-[1-carboxy-1-(phosphonooxy)ethyl]sulfanylpropanoic acid" EXACT RESID-systematic []
-synonym: "2-([(2R)-2-amino-2-carboxyethyl]sulfanyl)-2-(phosphonooxy)propanoic acid" EXACT RESID-alternate []
-synonym: "2-([(2R)-2-azanyl-2-carboxyethyl]sulfanyl)-2-(phosphonooxy)propanoic acid" EXACT RESID-alternate []
-synonym: "2-(S-L-cysteinyl)pyruvic acid O-phosphothioketal" EXACT RESID-name []
-synonym: "cysteinyl pyruvate O-phosphothioketal" EXACT RESID-alternate []
-synonym: "MOD_RES 2-(S-cysteinyl)pyruvic acid O-phosphothioketal" EXACT UniProt-feature []
-synonym: "phosphoenolpyruvate cysteine adduct" EXACT RESID-alternate []
-synonym: "phospholactoyl cysteine adduct" EXACT RESID-alternate []
-synonym: "S-[1-carboxy-1-(phosphonooxy)ethyl]cysteine" EXACT RESID-alternate []
-synonym: "SPEPCys" EXACT PSI-MOD-label []
-property_value: DiffAvg "168.04" xsd:float
-property_value: DiffFormula "C 3 H 5 N 0 O 6 P 1 S 0" xsd:string
-property_value: DiffMono "167.982375" xsd:float
-property_value: Formula "C 6 H 10 N 1 O 7 P 1 S 1" xsd:string
-property_value: MassAvg "271.18" xsd:float
-property_value: MassMono "270.991559" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0424
-is_a: MOD:00861
-is_a: MOD:00905
-
-[Term]
-id: MOD:00798
-name: half cystine
-def: "A protein modification that can be regarded as effectively either one half of a cystine cross-link, or a cysteine residue with one hydrogen atom or proton removed." [PubMed:1988019, PubMed:2001356, PubMed:2076469, PubMed:3083866, PubMed:366603, PubMed:7918467, PubMed:8344916, Unimod:374]
-synonym: "Dehydro" RELATED PSI-MS-label []
-synonym: "Half of a disulfide bridge" RELATED Unimod-description []
-property_value: DiffAvg "-1.01" xsd:float
-property_value: DiffFormula "C 0 H -1 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "-1.007825" xsd:float
-property_value: Formula "C 3 H 4 N 1 O 1 S 1" xsd:string
-property_value: MassAvg "102.13" xsd:float
-property_value: MassMono "102.001360" xsd:float
-property_value: Origin "C" xsd:string
-xref: Unimod:374
-is_a: MOD:00905
-
-[Term]
-id: MOD:00799
-name: S-galactosyl-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-galactosyl-L-cysteine." [PubMed:11945907, RESID:AA0392]
-comment: The reported peptide has not been isolated or characterized in subsequent work, and the peptide sequence has not been found in the human proteome. This is a deprecated entry in RESID. It probably does not occur naturally [JSG].
-synonym: "(2R)-2-amino-3-(D-galactopyranosylsulfanyl)propanoic acid" EXACT RESID-systematic []
-synonym: "S-(beta-D-galactopyranosyl)cysteine" EXACT RESID-alternate []
-synonym: "S-galactosyl-L-cysteine" EXACT RESID-name []
-synonym: "S-glycosyl-cysteine" EXACT RESID-alternate []
-synonym: "SGalCys" EXACT PSI-MOD-label []
-synonym: "CARBOHYD S-linked (Gal) cysteine" EXACT UniProt-feature []
-property_value: DiffAvg "162.14" xsd:float
-property_value: DiffFormula "C 6 H 10 N 0 O 5 S 0" xsd:string
-property_value: DiffMono "162.052823" xsd:float
-property_value: Formula "C 9 H 15 N 1 O 6 S 1" xsd:string
-property_value: MassAvg "265.28" xsd:float
-property_value: MassMono "265.062008" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: uniprot.ptm:PTM-0624
-is_a: MOD:00426
-is_a: MOD:00476
-is_a: MOD:00905
-
-[Term]
-id: MOD:00800
-name: L-cysteinyl-L-histidino-homocitryl vanadium heptairon nonasulfide
-def: "A protein modification that effectively converts an L-cysteine residue, an L-histidine residue, homocitric acid and a one-vanadium seven-iron nine-sulfur cluster to L-cysteinyl-L-histidino-homocitryl vanadium heptairon nonasulfide." [PubMed:2345152, RESID:AA0393]
-comment: Cross-link 2; incidental to RESID:AA0300.
-synonym: "CysHis-[V7Fe9S]" EXACT PSI-MOD-label []
-synonym: "L-cysteinyl-L-histidino-homocitryl vanadium heptairon nonasulfide carbide" EXACT RESID-name []
-synonym: "nitrogenase iron-vanadium cofactor" EXACT RESID-alternate []
-property_value: DiffAvg "932.51" xsd:float
-property_value: DiffFormula "C 7 Fe 7 H 6 N 0 O 7 S 9 V 1" xsd:string
-property_value: DiffMono "932.248513" xsd:float
-property_value: Formula "C 16 Fe 7 H 18 N 4 O 9 S 10 V 1" xsd:string
-property_value: MassAvg "1172.80" xsd:float
-property_value: MassMono "1172.316610" xsd:float
-property_value: Origin "C, H" xsd:string
-property_value: Source "hypothetical" xsd:string
-is_a: MOD:00739
-is_a: MOD:00772
-is_a: MOD:02067
-is_a: MOD:02070
-
-[Term]
-id: MOD:00801
-name: L-cysteinyl-L-histidino-homocitryl octairon nonasulfide
-def: "A protein modification that effectively converts an L-cysteine residue, an L-histidine residue, homocitric acid and an eight-iron nine-sulfur cluster to L-cysteinyl-L-histidino-homocitryl octairon nonasulfide." [PubMed:8392330, RESID:AA0394]
-comment: Cross-link 2; incidental to RESID:AA0300.
-synonym: "CysHis-[8Fe9S]" EXACT PSI-MOD-label []
-synonym: "L-cysteinyl-L-histidino-homocitryl octairon nonasulfide carbide" EXACT RESID-name []
-synonym: "nitrogenase iron-iron cofactor" EXACT RESID-alternate []
-property_value: DiffAvg "937.42" xsd:float
-property_value: DiffFormula "C 7 Fe 8 H 6 N 0 O 7 S 9" xsd:string
-property_value: DiffMono "937.240588" xsd:float
-property_value: FormalCharge "2-" xsd:string
-property_value: Formula "C 16 Fe 8 H 18 N 4 O 9 S 10" xsd:string
-property_value: MassAvg "1177.70" xsd:float
-property_value: MassMono "1177.308685" xsd:float
-property_value: Origin "C, H" xsd:string
-property_value: Source "hypothetical" xsd:string
-is_a: MOD:00739
-is_a: MOD:02067
-is_a: MOD:02070
-
-[Term]
-id: MOD:00802
-name: L-histidino vanadium tetraoxide
-def: "a protein modification that effectively converts an L-histidine residue to L-histidino vanadium tetraoxide" [PubMed:10543953, PubMed:16494433, PubMed:8552646, RESID:AA0395]
-synonym: "(4-[(2S)-2-amino-2-carboxyethyl]-1H-imidazol-1-yl) (dihydroxy)dioxovanadium" EXACT RESID-alternate []
-synonym: "1'-vanadato-L-histidine" EXACT RESID-alternate []
-synonym: "bromoperoxidase vanadium cofactor" EXACT RESID-alternate []
-synonym: "chloroperoxidase vanadium cofactor" EXACT RESID-alternate []
-synonym: "dihydrogen (4-[(2S)-2-amino-2-carboxyethyl]-1H-imidazol-1-yl) (tetraoxido)vanadate" EXACT RESID-systematic []
-synonym: "haloperoxidase vanadium cofactor" EXACT RESID-alternate []
-synonym: "histidine-1-vanadate" EXACT RESID-alternate []
-synonym: "histidine-N(epsilon)-vanadate" EXACT RESID-alternate []
-synonym: "histidine-N1'-vanadate" EXACT RESID-alternate []
-synonym: "L-histidino vanadium tetraoxide" EXACT RESID-name []
-synonym: "N(tau)-vanadatohistidine" EXACT RESID-alternate []
-synonym: "NtauH2VO4His" EXACT PSI-MOD-label []
-synonym: "tele-vanadatohistidine" EXACT RESID-alternate []
-property_value: DiffAvg "116.95" xsd:float
-property_value: DiffFormula "C 0 H 2 N 0 O 4 V 1" xsd:string
-property_value: DiffMono "116.939268" xsd:float
-property_value: Formula "C 6 H 9 N 3 O 5 V 1" xsd:string
-property_value: MassAvg "254.10" xsd:float
-property_value: MassMono "253.998180" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00772
-is_a: MOD:02070
-
-[Term]
-id: MOD:00803
-name: 3-(S-L-cysteinyl)-L-tyrosine
-def: "A protein modification that effectively cross-links an L-cysteine residue and an L-tyrosine residue by a thioether bond to form 3-(S-L-cysteinyl)-L-tyrosine." [PubMed:15342250, RESID:AA0396]
-comment: Cross-link 2.
-synonym: "(2S,3R)-2-amino-3-([(2R)-2-amino-2-carboxyethyl]sulfanyl)-3-(4-hydroxyphenyl)propanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-3-(2-amino-2-carboxyethylthio)-3-(4-hydroxyphenyl)propanoic acid" EXACT RESID-alternate []
-synonym: "3-(L-cystein-S-yl)-L-tyrosine" EXACT RESID-name []
-synonym: "CROSSLNK 3-(S-cysteinyl)-tyrosine (Cys-Tyr)" EXACT UniProt-feature []
-synonym: "S-(tyros-3'-yl)cysteine" EXACT RESID-alternate []
-synonym: "XLNKSCys3Tyr" EXACT PSI-MOD-label []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 12 H 12 N 2 O 3 S 1" xsd:string
-property_value: MassAvg "264.30" xsd:float
-property_value: MassMono "264.056863" xsd:float
-property_value: Origin "C, Y" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0020
-is_a: MOD:02058
-is_a: MOD:01993
-
-[Term]
-id: MOD:00804
-name: O-glucosyl-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O3-beta-glucosylated L-serine." [PubMed:10734111, PubMed:2105311, PubMed:2511201, RESID:AA0397]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-(beta-D-glucopyranosyloxy)propanoic acid" EXACT RESID-systematic []
-synonym: "CARBOHYD O-linked (Glc) serine" EXACT UniProt-feature []
-synonym: "CARBOHYD O-linked (Hex)" EXACT UniProt-feature []
-synonym: "O-glucosyl-L-serine" EXACT RESID-name []
-synonym: "O-glycosylserine" EXACT RESID-alternate []
-synonym: "O3-glucosylserine" EXACT RESID-alternate []
-synonym: "OGlcSer" EXACT PSI-MOD-label []
-property_value: DiffAvg "162.14" xsd:float
-property_value: DiffFormula "C 6 H 10 N 0 O 5" xsd:string
-property_value: DiffMono "162.052823" xsd:float
-property_value: Formula "C 9 H 15 N 1 O 7" xsd:string
-property_value: MassAvg "249.22" xsd:float
-property_value: MassMono "249.084852" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0573
-is_a: MOD:00002
-is_a: MOD:00433
-
-[Term]
-id: MOD:00805
-name: O-(N-acetylamino)glucosyl-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O3-(N-acetylaminoglucosyl)-L-serine." [PubMed:3086323, PubMed:8404891, RESID:AA0398]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-(2-acetamido-2-deoxy-beta-D-glucopyranosyloxy)propanoic acid" EXACT RESID-systematic []
-synonym: "CARBOHYD O-linked (GlcNAc) serine" EXACT UniProt-feature []
-synonym: "CARBOHYD O-linked (HexNAc)" EXACT UniProt-feature []
-synonym: "HexNAc" RELATED PSI-MS-label []
-synonym: "O-(2-acetylamino-2-deoxy-beta-D-glucopyranosyl)-L-serine" EXACT RESID-alternate []
-synonym: "O-(N-acetylamino)glucosyl-L-serine" EXACT RESID-name []
-synonym: "O-(N-acetylglucosaminyl)serine" EXACT RESID-alternate []
-synonym: "O-glycosylserine" EXACT RESID-alternate []
-synonym: "O-seryl-beta-N-acetylglucosaminide" EXACT RESID-alternate []
-synonym: "O3-(2-acetamido-2-deoxy-beta-D-glucopyranosyl)-L-serine" EXACT RESID-alternate []
-synonym: "O3-(N-acetylglucosaminyl)serine" EXACT RESID-alternate []
-synonym: "OGlcNAcSer" EXACT PSI-MOD-label []
-property_value: DiffAvg "203.19" xsd:float
-property_value: DiffFormula "C 8 H 13 N 1 O 5" xsd:string
-property_value: DiffMono "203.079373" xsd:float
-property_value: Formula "C 11 H 18 N 2 O 7" xsd:string
-property_value: MassAvg "290.27" xsd:float
-property_value: MassMono "290.111401" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0580
-is_a: MOD:00448
-is_a: MOD:01675
-
-[Term]
-id: MOD:00806
-name: O-(N-acetylamino)glucosyl-L-threonine
-def: "A protein modification that effectively converts an L-threonine residue to O3-(N-acetylaminoglucosyl)-L-threonine." [PubMed:3086323, PubMed:8404891, RESID:AA0399]
-subset: PSI-MOD-slim
-synonym: "(2S,3R)-2-amino-3-(2-acetamido-2-deoxy-beta-D-glucopyranosyloxy)butanoic acid" EXACT RESID-systematic []
-synonym: "CARBOHYD O-linked (GlcNAc) threonine" EXACT UniProt-feature []
-synonym: "CARBOHYD O-linked (HexNAc)" EXACT UniProt-feature []
-synonym: "HexNAc" RELATED PSI-MS-label []
-synonym: "O-(2-acetylamino-2-deoxy-beta-D-glucopyranosyl)-L-threonine" EXACT RESID-alternate []
-synonym: "O-(N-acetylamino)glucosyl-L-threonine" EXACT RESID-name []
-synonym: "O-(N-acetylglucosaminyl)-L-threonine" EXACT RESID-alternate []
-synonym: "O-glycosylthreonine" EXACT RESID-alternate []
-synonym: "O-threonyl-beta-N-acetylglucosaminide" EXACT RESID-alternate []
-synonym: "O3-(2-acetamido-2-deoxy-beta-D-glucopyranosyl)-L-threonine" EXACT RESID-alternate []
-synonym: "O3-(N-acetylglucosaminyl)threonine" EXACT RESID-alternate []
-synonym: "OGlcNAcThr" EXACT PSI-MOD-label []
-property_value: DiffAvg "203.19" xsd:float
-property_value: DiffFormula "C 8 H 13 N 1 O 5" xsd:string
-property_value: DiffMono "203.079373" xsd:float
-property_value: Formula "C 12 H 20 N 2 O 7" xsd:string
-property_value: MassAvg "304.30" xsd:float
-property_value: MassMono "304.127051" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0582
-is_a: MOD:00448
-is_a: MOD:01676
-
-[Term]
-id: MOD:00807
-name: pyruvic acid (Ser)
-def: "A protein modification that effectively converts an L-serine residue to pyruvic acid." [DeltaMass:23, PubMed:10085076, PubMed:3042771, PubMed:8464063, RESID:AA0127#SER, Unimod:385#S]
-comment: DeltaMass gives mass 70 and difference mass -16 with no formula
-subset: PSI-MOD-slim
-synonym: "2-oxopropanoic acid" EXACT RESID-systematic []
-synonym: "MOD_RES Pyruvic acid (Ser)" EXACT UniProt-feature []
-synonym: "Pyruvate" EXACT DeltaMass-label []
-synonym: "pyruvic acid" EXACT RESID-name []
-synonym: "Pyruvoyl- (Serine)" EXACT DeltaMass-label []
-property_value: DiffAvg "-17.03" xsd:float
-property_value: DiffFormula "C 0 H -3 N -1 O 0" xsd:string
-property_value: DiffMono "-17.026549" xsd:float
-property_value: Formula "C 3 H 3 O 2" xsd:string
-property_value: MassAvg "71.06" xsd:float
-property_value: MassMono "71.013304" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:385
-xref: uniprot.ptm:PTM-0266
-is_a: MOD:00916
-is_a: MOD:01154
-is_a: MOD:01160
-
-[Term]
-id: MOD:00808
-name: O-galactosyl-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O3-galactosylserine." [PubMed:666730, RESID:AA0400]
-synonym: "(2S)-2-amino-3-(alpha-D-galactopyranosyloxy)propanoic acid" EXACT RESID-systematic []
-synonym: "CARBOHYD O-linked (Gal) serine" EXACT UniProt-feature []
-synonym: "CARBOHYD O-linked (Hex)" EXACT UniProt-feature []
-synonym: "O-galactosyl-L-serine" EXACT RESID-name []
-synonym: "O-glycosylserine" EXACT RESID-alternate []
-synonym: "O3-galactosylserine" EXACT RESID-alternate []
-synonym: "OGalSer" EXACT PSI-MOD-label []
-property_value: DiffAvg "162.14" xsd:float
-property_value: DiffFormula "C 6 H 10 N 0 O 5" xsd:string
-property_value: DiffMono "162.052823" xsd:float
-property_value: Formula "C 9 H 15 N 1 O 7" xsd:string
-property_value: MassAvg "249.22" xsd:float
-property_value: MassMono "249.084852" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0560
-is_a: MOD:00002
-is_a: MOD:00476
-
-[Term]
-id: MOD:00809
-name: O-galactosyl-L-threonine
-def: "A protein modification that effectively converts an L-threonine residue to O3-galactosylthreonine." [PubMed:2673008, RESID:AA0401]
-synonym: "(2S,3R)-2-amino-3-(alpha-D-galactopyranosyloxy)butanoic acid" EXACT RESID-systematic []
-synonym: "CARBOHYD O-linked (Gal) threonine" EXACT UniProt-feature []
-synonym: "CARBOHYD O-linked (Hex)" EXACT UniProt-feature []
-synonym: "O-galactosyl-L-threonine" EXACT RESID-name []
-synonym: "O-glycosylthreonine" EXACT RESID-alternate []
-synonym: "O3-galactosylthreonine" EXACT RESID-alternate []
-synonym: "OGalThr" EXACT PSI-MOD-label []
-property_value: DiffAvg "162.14" xsd:float
-property_value: DiffFormula "C 6 H 10 N 0 O 5" xsd:string
-property_value: DiffMono "162.052823" xsd:float
-property_value: Formula "C 10 H 17 N 1 O 7" xsd:string
-property_value: MassAvg "263.25" xsd:float
-property_value: MassMono "263.100502" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0562
-is_a: MOD:00476
-is_a: MOD:01348
-
-[Term]
-id: MOD:00810
-name: O-mannosyl-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O3-mannosylserine." [PubMed:391559, RESID:AA0402]
-synonym: "(2S)-2-amino-3-(alpha-D-mannopyranosyloxy)propanoic acid" EXACT RESID-systematic []
-synonym: "CARBOHYD O-linked (Hex)" EXACT UniProt-feature []
-synonym: "CARBOHYD O-linked (Man) serine" EXACT UniProt-feature []
-synonym: "O-glycosylserine" EXACT RESID-alternate []
-synonym: "O-mannopyranosylserine" EXACT RESID-alternate []
-synonym: "O-mannosyl-L-serine" EXACT RESID-name []
-synonym: "O3-mannosylserine" EXACT RESID-alternate []
-synonym: "OManSer" EXACT PSI-MOD-label []
-property_value: DiffAvg "162.14" xsd:float
-property_value: DiffFormula "C 6 H 10 N 0 O 5" xsd:string
-property_value: DiffMono "162.052823" xsd:float
-property_value: Formula "C 9 H 15 N 1 O 7" xsd:string
-property_value: MassAvg "249.22" xsd:float
-property_value: MassMono "249.084852" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0588
-is_a: MOD:00002
-is_a: MOD:00595
-
-[Term]
-id: MOD:00811
-name: O-mannosyl-L-threonine
-def: "a protein modification that effectively forms a O3-mannosylthreonine" [PubMed:391559, RESID:AA0403]
-synonym: "(2S,3R)-2-amino-3-(alpha-D-mannopyranosyloxy)butanoic acid" EXACT RESID-systematic []
-synonym: "CARBOHYD O-linked (Hex)" EXACT UniProt-feature []
-synonym: "CARBOHYD O-linked (Man) threonine" EXACT UniProt-feature []
-synonym: "O-glycosylthreonine" EXACT RESID-alternate []
-synonym: "O-mannosyl-L-threonine" EXACT RESID-name []
-synonym: "O3-mannosylthreonine" EXACT RESID-alternate []
-synonym: "OManThr" EXACT PSI-MOD-label []
-property_value: DiffAvg "162.14" xsd:float
-property_value: DiffFormula "C 6 H 10 N 0 O 5" xsd:string
-property_value: DiffMono "162.052823" xsd:float
-property_value: Formula "C 10 H 17 N 1 O 7" xsd:string
-property_value: MassAvg "263.25" xsd:float
-property_value: MassMono "263.100502" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0591
-is_a: MOD:00595
-is_a: MOD:01348
-
-[Term]
-id: MOD:00812
-name: O-fucosyl-L-serine
-def: "A protein modification that effectively converts an L-serine residue to an O-fucosylserine." [PubMed:10734111, PubMed:11067851, PubMed:11344537, PubMed:12096136, PubMed:1517205, PubMed:15189151, PubMed:1904059, PubMed:3311742, PubMed:3578767, RESID:AA0404, Unimod:295#S]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-(6-deoxy-alpha-D-galactopyranosyloxy)propanoic acid" EXACT RESID-systematic []
-synonym: "CARBOHYD O-linked (dHex)" EXACT UniProt-feature []
-synonym: "CARBOHYD O-linked (Fuc)" EXACT UniProt-feature []
-synonym: "dHex" RELATED PSI-MS-label []
-synonym: "Fucose" RELATED Unimod-description []
-synonym: "O-fucosyl-L-serine" EXACT RESID-name []
-synonym: "O-glycosylserine" EXACT RESID-alternate []
-synonym: "O3-fucosylserine" EXACT RESID-alternate []
-synonym: "OFucSer" EXACT PSI-MOD-label []
-synonym: "CARBOHYD O-linked (Fuc) serine" EXACT UniProt-feature []
-property_value: DiffAvg "146.14" xsd:float
-property_value: DiffFormula "C 6 H 10 N 0 O 4" xsd:string
-property_value: DiffMono "146.057909" xsd:float
-property_value: Formula "C 9 H 15 N 1 O 6" xsd:string
-property_value: MassAvg "233.22" xsd:float
-property_value: MassMono "233.089937" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:295
-xref: uniprot.ptm:PTM-0550
-is_a: MOD:00002
-is_a: MOD:00614
-
-[Term]
-id: MOD:00813
-name: O-fucosyl-L-threonine
-def: "A protein modification that effectively converts an threonine residue to an O-fucosylthreonine." [PubMed:11344537, PubMed:11857757, PubMed:15189151, PubMed:1740125, PubMed:1900431, RESID:AA0405, Unimod:295#T]
-subset: PSI-MOD-slim
-synonym: "(2S,3R)-2-amino-3-(6-deoxy-alpha-D-galactopyranosyloxy)butanoic acid" EXACT RESID-systematic []
-synonym: "CARBOHYD O-linked (dHex)" EXACT UniProt-feature []
-synonym: "CARBOHYD O-linked (Fuc) threonine" EXACT UniProt-feature []
-synonym: "dHex" RELATED PSI-MS-label []
-synonym: "Fucose" RELATED Unimod-description []
-synonym: "O-fucosyl-L-threonine" EXACT RESID-name []
-synonym: "O-glycosylthreonine" EXACT RESID-alternate []
-synonym: "O3-fucosylthreonine" EXACT RESID-alternate []
-synonym: "OFucThr" EXACT PSI-MOD-label []
-property_value: DiffAvg "146.14" xsd:float
-property_value: DiffFormula "C 6 H 10 N 0 O 4" xsd:string
-property_value: DiffMono "146.057909" xsd:float
-property_value: Formula "C 10 H 17 N 1 O 6" xsd:string
-property_value: MassAvg "247.25" xsd:float
-property_value: MassMono "247.105587" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:295
-xref: uniprot.ptm:PTM-0552
-is_a: MOD:00005
-is_a: MOD:00614
-
-[Term]
-id: MOD:00814
-name: O-xylosyl-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O3-xylosylserine." [PubMed:8747463, RESID:AA0406]
-comment: One glycosylated serine with weak electron density was modeled as O3-alpha-xylosylserine, while O3-alpha-mannosyl serine and threonine were modeled at ten other positions. The authors do not discuss this exception or provide chemical evidence for it. Since an O3-xylosyl serine modification has not been reported in any other fungal proteins, the modification is probably also an O3-alpha-mannosyl serine, see MOD:00810 [JSG].
-synonym: "(2S)-2-amino-3-(alpha-D-xylopyranosyloxy)propanoic acid" EXACT RESID-systematic []
-synonym: "O-(beta-D-xylopyranosyl)-L-serine" EXACT RESID-alternate []
-synonym: "O-glycosylserine" EXACT RESID-alternate []
-synonym: "O-xylosyl-L-serine" EXACT RESID-name []
-synonym: "O3-xylosylserine" EXACT RESID-alternate []
-synonym: "OXylSer" EXACT PSI-MOD-label []
-synonym: "CARBOHYD O-linked (Xyl) serine" EXACT UniProt-feature []
-property_value: DiffAvg "132.12" xsd:float
-property_value: DiffFormula "C 5 H 8 N 0 O 4" xsd:string
-property_value: DiffMono "132.042259" xsd:float
-property_value: Formula "C 8 H 13 N 1 O 6" xsd:string
-property_value: MassAvg "219.19" xsd:float
-property_value: MassMono "219.074287" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-xref: uniprot.ptm:PTM-0598
-is_a: MOD:00002
-
-[Term]
-id: MOD:00815
-name: molybdopterin
-def: "OBSOLETE because redundant with MOD:00151. Remap to MOD:00151." [PubMed:14527393, PubMed:7878465, PubMed:9428520]
-property_value: DiffAvg "520.27" xsd:float
-property_value: DiffFormula "C 10 H 11 Mo 1 N 5 O 8 P 1 S 2" xsd:string
-property_value: DiffMono "521.884074" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-replaced_by: MOD:00151
-is_obsolete: true
-
-[Term]
-id: MOD:00816
-name: S-stearoyl-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-stearoyl-L-cysteine." [DeltaMass:0, PubMed:2371783, PubMed:3143715, PubMed:8761467, RESID:AA0407]
-comment: From DeltaMass: Average Mass: 266
-subset: PSI-MOD-slim
-synonym: "(R)-2-amino-3-(octadecanoylsulfanyl)propanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-3-(octadecanoylthio)propanoic acid" EXACT RESID-alternate []
-synonym: "cysteine octadecanoate thioester" EXACT RESID-alternate []
-synonym: "cysteine stearate thioester" EXACT RESID-alternate []
-synonym: "LIPID S-stearoyl cysteine" EXACT UniProt-feature []
-synonym: "S-stearoyl-L-cysteine" EXACT RESID-name []
-synonym: "SSteCys" EXACT PSI-MOD-label []
-synonym: "Stearoylation" EXACT DeltaMass-label []
-property_value: DiffAvg "266.47" xsd:float
-property_value: DiffFormula "C 18 H 34 N 0 O 1 S 0" xsd:string
-property_value: DiffMono "266.260966" xsd:float
-property_value: Formula "C 21 H 39 N 1 O 2 S 1" xsd:string
-property_value: MassAvg "369.61" xsd:float
-property_value: MassMono "369.270150" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0283
-is_a: MOD:02005
-is_a: MOD:02006
-
-[Term]
-id: MOD:00817
-name: 3'-geranyl-2',3'-dihydro-2',N2-cyclo-L-tryptophan
-def: "A protein modification that effectively converts an L-tryptophan residue to 3'-geranyl-2',3'-dihydro-2',N2-cyclo-L-tryptophan." [ChEBI:35304, PubMed:16407988, PubMed:8168130, RESID:AA0408]
-synonym: "(2S,3aR,8aS)-3a-[(2E)-3,7-dimethylocta-2,6-dien-1-yl]-1,2,3,3a,8,8a-hexahydropyrrolo[2,3-b]indole-2-carboxylic acid" EXACT RESID-systematic []
-synonym: "(2S,3R)-3-geranyl-2,3-dihydro-2,N(alpha)-cyclo-L-tryptophan" EXACT RESID-alternate []
-synonym: "3'-geranyl-2',3'-dihydro-2',N2-cyclo-L-tryptophan" EXACT RESID-name []
-synonym: "3'Ger2'N2cycTrp" EXACT PSI-MOD-label []
-synonym: "LIPID 3'-geranyl-2',N2-cyclotryptophan" EXACT UniProt-feature []
-property_value: DiffAvg "136.24" xsd:float
-property_value: DiffFormula "C 10 H 16 N 0 O 0" xsd:string
-property_value: DiffMono "136.125201" xsd:float
-property_value: Formula "C 21 H 26 N 2 O 1" xsd:string
-property_value: MassAvg "322.45" xsd:float
-property_value: MassMono "322.204513" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0026
-is_a: MOD:00601
-is_a: MOD:01115
-
-[Term]
-id: MOD:00818
-name: glycosylphosphatidylinositolated residue
-def: "A protein modification that effectively converts a residue to a glycosylphosphatidylinositolethanolamidated." [PubMed:12643538, Unimod:394#C-term]
-synonym: "glycosylphosphatidylinositol" RELATED Unimod-description []
-synonym: "GPIanchor" RELATED Unimod-interim []
-synonym: "GPIRes" EXACT PSI-MOD-label []
-synonym: "LIPID GPI-anchor amidated carboxyl end" EXACT UniProt-feature []
-property_value: DiffAvg "123.05" xsd:float
-property_value: DiffFormula "C 2 H 6 N 1 O 3 P 1" xsd:string
-property_value: DiffMono "123.008530" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: Unimod:394
-xref: uniprot.ptm:PTM-0139
-is_a: MOD:00764
-is_a: MOD:00861
-is_a: MOD:01155
-
-[Term]
-id: MOD:00819
-name: L-2-aminobutanoic acid (Glu)
-def: "A protein modification that effectively converts an L-glutamic acid residue to L-2-aminobutanoic acid." [ChEBI:35619, DeltaMass:0, PubMed:11740505, RESID:AA0409]
-synonym: "(S)-2-aminobutanoic acid" EXACT RESID-systematic []
-synonym: "Abu" EXACT DeltaMass-label []
-synonym: "Abu" EXACT PSI-MOD-label []
-synonym: "alpha-amino-n-butyric acid" EXACT PSI-MOD-alternate []
-synonym: "alpha-aminobutyric acid" EXACT PSI-MOD-alternate []
-synonym: "butyrine" EXACT PSI-MOD-alternate []
-synonym: "dCbxGlu" EXACT PSI-MOD-alternate []
-synonym: "L-2-amino-n-butyric acid" EXACT RESID-alternate []
-synonym: "L-2-aminobutanoic acid" EXACT RESID-name []
-synonym: "L-2-aminobutyric acid" EXACT RESID-alternate []
-synonym: "L-alpha-amino-n-butyric acid" EXACT RESID-alternate []
-synonym: "L-alpha-aminobutyric acid" EXACT RESID-alternate []
-synonym: "L-butyrine" EXACT RESID-alternate []
-property_value: DiffAvg "-44.01" xsd:float
-property_value: DiffFormula "C -1 H 0 N 0 O -2" xsd:string
-property_value: DiffMono "-43.989829" xsd:float
-property_value: Formula "C 4 H 7 N 1 O 1" xsd:string
-property_value: MassAvg "85.11" xsd:float
-property_value: MassMono "85.052764" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00906
-
-[Term]
-id: MOD:00820
-name: 2-imino-alanine 5-imidazolinone glycine
-def: "A protein modification that effectively crosslinks an L-aspartic acid residue and a glycine residue to form 2-imino-alanine 5-imidazolinone glycine." [PubMed:16627946, RESID:AA0410]
-comment: Cross-link 2; carboxamidine.
-synonym: "(2-ethanimidoyl-5-oxo-4,5-dihydro-1H-imidazol-1-yl)acetic acid" EXACT RESID-systematic []
-synonym: "2,N-didehydroalanyl-5-imidazolinone glycine" EXACT RESID-alternate []
-synonym: "2-(1-iminoethyl)-1-carboxymethyl-1-imidazolin-5-one" EXACT RESID-alternate []
-synonym: "2-imino-alanine 5-imidazolinone glycine" EXACT RESID-name []
-synonym: "2-imino-alanyl-5-imidazolinone glycine" EXACT RESID-alternate []
-synonym: "[2-(1-iminoethyl)-5-oxo-4,5-dihydro-imidazol-1-yl]-acetic acid" EXACT RESID-alternate []
-synonym: "alanyl-5-imidazolinone glycine" EXACT RESID-alternate []
-synonym: "para-hydroxybenzylidene-imidazolidinone chromophore" EXACT RESID-alternate []
-synonym: "red fluorescent protein zRFP574 chromophore" EXACT RESID-alternate []
-property_value: DiffAvg "-64.04" xsd:float
-property_value: DiffFormula "C -1 H -4 N 0 O -3" xsd:string
-property_value: DiffMono "-64.016044" xsd:float
-property_value: Formula "C 5 H 4 N 2 O 1" xsd:string
-property_value: MassAvg "108.10" xsd:float
-property_value: MassMono "108.032363" xsd:float
-property_value: Origin "D, G" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:02043
-is_a: MOD:02047
-is_a: MOD:01882
-
-[Term]
-id: MOD:00821
-name: S-(L-alanyl)-L-cysteine
-def: "A protein modification that effectively crosslinks an L-alanine residue and an L-cysteine residue by a thioester bond to form S-(L-alanyl)-L-cysteine." [PubMed:11807079, RESID:AA0411]
-comment: Cross-link 2.
-synonym: "(2R)-2-amino-3-([(2S)-2-aminopropanoyl]sulfanyl)propanoic acid" EXACT RESID-systematic []
-synonym: "alanine cysteine thioester" EXACT RESID-alternate []
-synonym: "CROSSLNK Alanyl cysteine thioester (Cys-Ala)" EXACT UniProt-feature []
-synonym: "S-(2-aminopropanoyl)cysteine" EXACT RESID-alternate []
-synonym: "S-(L-alanyl)-L-cysteine" EXACT RESID-name []
-synonym: "XLNK1AlaSCys" EXACT PSI-MOD-label []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 6 H 9 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "173.21" xsd:float
-property_value: MassMono "173.038474" xsd:float
-property_value: Origin "A, C" xsd:string
-property_value: Source "hypothetical" xsd:string
-property_value: TermSpec "C-term" xsd:string
-is_a: MOD:00395
-is_a: MOD:02040
-is_a: MOD:00954
-
-[Term]
-id: MOD:00822
-name: S-(L-leucyl)-L-cysteine
-def: "A protein modification that effectively crosslinks an L-leucine residue and an L-cysteine residue by a thioester bond to form S-(L-leucyl)-L-cysteine." [PubMed:12591958, RESID:AA0412]
-comment: Cross-link 2.
-synonym: "(2R)-2-amino-3-([(2S)-2-amino-4-methylpentanoyl]sulfanyl)propanoic acid" EXACT RESID-systematic []
-synonym: "CROSSLNK Leucyl cysteine thioester (Cys-Leu)" EXACT UniProt-feature []
-synonym: "leucine cysteine thioester" EXACT RESID-alternate []
-synonym: "S-(2-amino-4-methylpentanoyl)cysteine" EXACT RESID-alternate []
-synonym: "S-(L-leucyl)-L-cysteine" EXACT RESID-name []
-synonym: "XLNK1LeuSCys" EXACT PSI-MOD-label []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 9 H 15 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "215.29" xsd:float
-property_value: MassMono "215.085424" xsd:float
-property_value: Origin "C, L" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-is_a: MOD:00395
-is_a: MOD:02050
-is_a: MOD:00954
-
-[Term]
-id: MOD:00823
-name: S-(L-methionyl)-L-cysteine
-def: "A protein modification that effectively crosslinks an L-methionine residue and an L-cysteine residue by a thioester bond to form S-(L-methionyl)-L-cysteine." [PubMed:12146974, RESID:AA0413]
-comment: Cross-link 2.
-synonym: "(2R)-2-amino-3-([(2S)-2-amino-4-(methylsulfanyl)butanoyl]sulfanyl)propanoic acid" EXACT RESID-systematic []
-synonym: "CROSSLNK Methionyl cysteine thioester (Cys-Met)" EXACT UniProt-feature []
-synonym: "methionine cysteine thioester" EXACT RESID-alternate []
-synonym: "S-(2-amino-4-methylthiobutanoyl)cysteine" EXACT RESID-alternate []
-synonym: "S-(L-methionyl)-L-cysteine" EXACT RESID-name []
-synonym: "XLNK1MetSCys" EXACT PSI-MOD-label []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 8 H 13 N 2 O 2 S 2" xsd:string
-property_value: MassAvg "233.32" xsd:float
-property_value: MassMono "233.041845" xsd:float
-property_value: Origin "C, M" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-is_a: MOD:00395
-is_a: MOD:02052
-is_a: MOD:00954
-
-[Term]
-id: MOD:00824
-name: dehydroalanine (Tyr)
-def: "A protein modification that effectively converts an L-tyrosine residue to dehydroalanine." [PubMed:10220322, PubMed:1547888, PubMed:1815586, PubMed:2914619, PubMed:6838602, PubMed:7947813, PubMed:8239649, RESID:AA0181#TYR, Unimod:400]
-comment: incidental to RESID:AA0178
-synonym: "2,3-didehydroalanine" EXACT RESID-alternate []
-synonym: "2-aminoacrylic acid" EXACT RESID-alternate []
-synonym: "2-aminopropenoic acid" EXACT RESID-systematic []
-synonym: "4-methylidene-imidazole-5-one (MIO) active site" EXACT RESID-alternate []
-synonym: "anhydroserine" EXACT RESID-alternate []
-synonym: "dehydroalanine" EXACT RESID-name []
-synonym: "Dha" EXACT RESID-alternate []
-synonym: "dHAla(Tyr)" EXACT PSI-MOD-label []
-property_value: DiffAvg "-94.11" xsd:float
-property_value: DiffFormula "C -6 H -6 N 0 O -1" xsd:string
-property_value: DiffMono "-94.041865" xsd:float
-property_value: Formula "C 3 H 3 N 1 O 1" xsd:string
-property_value: MassAvg "69.06" xsd:float
-property_value: MassMono "69.021464" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:400
-xref: uniprot.ptm:PTM-0647
-is_a: MOD:00919
-is_a: MOD:01168
-
-[Term]
-id: MOD:00825
-name: S-(L-phenylalanyl)-L-cysteine
-def: "A protein modification that effectively crosslinks an L-phenylalanine residue and an L-cysteine residue by a thioester bond to form S-(L-phenylalaninyl)-L-cysteine." [PubMed:12591958, RESID:AA0414]
-comment: Cross-link 2.
-synonym: "(2R)-2-amino-3-([(2S)-2-amino-3-phenylpropanoyl]sulfanyl)propanoic acid" EXACT RESID-systematic []
-synonym: "CROSSLNK Phenylalanyl cysteine thioester (Cys-Phe)" EXACT UniProt-feature []
-synonym: "phenylalanine cysteine thioester" EXACT RESID-alternate []
-synonym: "S-(2-amino-3-phenylpropanoyl)cysteine" EXACT RESID-alternate []
-synonym: "S-(L-phenylalanyl)-L-cysteine" EXACT RESID-name []
-synonym: "XLNK1PheSCys" EXACT PSI-MOD-label []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 12 H 13 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "249.31" xsd:float
-property_value: MassMono "249.069774" xsd:float
-property_value: Origin "C, F" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-is_a: MOD:00395
-is_a: MOD:02053
-is_a: MOD:00954
-
-[Term]
-id: MOD:00826
-name: S-(L-threonyl)-L-cysteine
-def: "A protein modification that effectively crosslinks an L-threonine residue and an L-cysteine residue by a thioester bond to form S-(L-threonyl)-L-cysteine." [PubMed:15268951, RESID:AA0415]
-comment: Cross-link 2.
-synonym: "(2R)-2-amino-3-([(2S,3R)-2-amino-3-hydroxybutanoyl]sulfanyl)propanoic acid" EXACT RESID-systematic []
-synonym: "CROSSLNK Threonyl cysteine thioester (Cys-Thr)" EXACT UniProt-feature []
-synonym: "S-(2-amino-3-hydroxybutanoyl)cysteine" EXACT RESID-alternate []
-synonym: "S-(L-threonyl)-L-cysteine" EXACT RESID-name []
-synonym: "threonine cysteine thioester" EXACT RESID-alternate []
-synonym: "XLNK1ThrSCys" EXACT PSI-MOD-label []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 7 H 11 N 2 O 3 S 1" xsd:string
-property_value: MassAvg "203.24" xsd:float
-property_value: MassMono "203.049038" xsd:float
-property_value: Origin "C, T" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-is_a: MOD:00395
-is_a: MOD:02056
-is_a: MOD:00954
-
-[Term]
-id: MOD:00827
-name: S-(L-tyrosyl)-L-cysteine
-def: "A protein modification that effectively crosslinks an L-tyrosine residue and an L-cysteine residue by a thioester bond to form S-(L-tyrosyl)-L-cysteine." [PubMed:11807079, RESID:AA0416]
-comment: Cross-link 2.
-synonym: "(2R)-2-amino-3-([(2S)-2-amino-3-(4-hydroxyphenyl)propanoyl]sulfanyl)propanoic acid" EXACT RESID-systematic []
-synonym: "CROSSLNK Tyrosyl cysteine thioester (Cys-Tyr)" EXACT UniProt-feature []
-synonym: "S-(L-tyrosyl)-L-cysteine" EXACT RESID-name []
-synonym: "S-[2-amino-3-(4-hydoxyphenyl)propanoyl]cysteine" EXACT RESID-alternate []
-synonym: "tyrosine cysteine thioester" EXACT RESID-alternate []
-synonym: "XLNK1TyrSCys" EXACT PSI-MOD-label []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 12 H 13 N 2 O 3 S 1" xsd:string
-property_value: MassAvg "265.31" xsd:float
-property_value: MassMono "265.064688" xsd:float
-property_value: Origin "C, Y" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-is_a: MOD:00395
-is_a: MOD:02058
-is_a: MOD:00954
-
-[Term]
-id: MOD:00828
-name: S-(L-tryptophanyl)-L-cysteine
-def: "A protein modification that effectively crosslinks an L-tryptophan residue and an L-cysteine residue by a thioester bond to form S-(L-tryptophanyl)-L-cysteine." [PubMed:16030216, RESID:AA0417]
-comment: Cross-link 2.
-synonym: "(2R)-2-amino-3-([(2S)-2-amino-3-(1H-indol-3-yl)propanoyl]sulfanyl)propanoic acid" EXACT RESID-systematic []
-synonym: "CROSSLNK Tryptophanyl cysteine thioester (Cys-Trp)" EXACT UniProt-feature []
-synonym: "S-(L-tryptophanyl)-L-cysteine" EXACT RESID-name []
-synonym: "S-[2-amino-3-(1H-indol-3-yl)propanoyl]cysteine" EXACT RESID-alternate []
-synonym: "tryptophan cysteine thioester" EXACT RESID-alternate []
-synonym: "XLNK1TrpSCys" EXACT PSI-MOD-label []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 14 H 14 N 3 O 2 S 1" xsd:string
-property_value: MassAvg "288.35" xsd:float
-property_value: MassMono "288.080673" xsd:float
-property_value: Origin "C, W" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-is_a: MOD:00395
-is_a: MOD:02057
-is_a: MOD:00954
-
-[Term]
-id: MOD:00829
-name: O-(L-phenylalanyl)-L-serine
-def: "A protein modification that effectively crosslinks an L-phenylalanine residue and an L-serine residue by an ester bond to form S-(L-phenylalaninyl)-L-serine." [PubMed:12591958, RESID:AA0418]
-comment: Cross-link 2.
-synonym: "(2S)-2-amino-3-([(2S)-2-amino-3-phenylpropanoyl]oxy)propanoic acid" EXACT RESID-systematic []
-synonym: "CROSSLNK Phenylalanyl serine ester (Ser-Phe)" EXACT UniProt-feature []
-synonym: "O-(2-amino-3-phenylpropanoyl)serine" EXACT RESID-alternate []
-synonym: "O-(L-phenylalanyl)-L-serine" EXACT RESID-name []
-synonym: "phenylalanine serine ester" EXACT RESID-alternate []
-synonym: "XLNK1PheOSer" EXACT PSI-MOD-label []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 12 H 13 N 2 O 3" xsd:string
-property_value: MassAvg "233.25" xsd:float
-property_value: MassMono "233.092617" xsd:float
-property_value: Origin "F, S" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-is_a: MOD:00885
-is_a: MOD:02053
-is_a: MOD:02055
-is_a: MOD:00954
-
-[Term]
-id: MOD:00830
-name: N-methyl-L-proline
-def: "A protein modification that effectively converts an L-proline residue to an N-methyl-L-proline." [PubMed:3127388, RESID:AA0419]
-comment: Polypeptides with monomethylated amino terminals can undergo premature cleavage during the coupling step of an Edman degradation. This can result in \"preview\" with both a residue and the following residue being seen from the first step on through a sequence [JSG].
-subset: PSI-MOD-slim
-synonym: "(S)-1-methylpyrrolidine-2-carboxylic acid" EXACT RESID-systematic []
-synonym: "1-methylpyrrolidine-2-carboxylic acid" EXACT RESID-alternate []
-synonym: "hygric acid" EXACT RESID-alternate []
-synonym: "MOD_RES N-methylproline" EXACT UniProt-feature []
-synonym: "N-methyl-L-proline" EXACT RESID-name []
-synonym: "N-methylated L-proline" EXACT PSI-MOD-alternate []
-synonym: "NMePro" EXACT PSI-MOD-label []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 6 H 10 N 1 O 1" xsd:string
-property_value: MassAvg "112.15" xsd:float
-property_value: MassMono "112.076239" xsd:float
-property_value: Origin "P" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0219
-is_a: MOD:01417
-is_a: MOD:01462
-is_a: MOD:01680
-
-[Term]
-id: MOD:00831
-name: N4-(N-acetylamino)glucosyl-L-asparagine
-def: "A protein modification that effectively converts an L-asparagine residue to N4-(N-acetylaminoglucosyl)-L-asparagine." [PubMed:111247, PubMed:1694179, PubMed:5490222, RESID:AA0151#var]
-subset: PSI-MOD-slim
-synonym: "HexNAc" RELATED PSI-MS-label []
-synonym: "N4GlcNAcAsn" EXACT PSI-MOD-label []
-synonym: "CARBOHYD N-linked (GlcNAc) asparagine" EXACT UniProt-feature []
-property_value: DiffAvg "203.19" xsd:float
-property_value: DiffFormula "C 8 H 13 N 1 O 5" xsd:string
-property_value: DiffMono "203.079373" xsd:float
-property_value: Formula "C 12 H 19 N 3 O 7" xsd:string
-property_value: MassAvg "317.30" xsd:float
-property_value: MassMono "317.122300" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0527
-is_a: MOD:00448
-is_a: MOD:01674
-
-[Term]
-id: MOD:00832
-name: N4-(N-acetylamino)galactosyl-L-asparagine
-def: "A protein modification that effectively converts an L-asparagine residue to N4-(N-acetaminogalactosyl)-L-asparagine." [PubMed:8262914, RESID:AA0420]
-synonym: "(2S)-2-amino-4-(2-acetamido-2-deoxy-beta-D-galactopyranosyl)amino-4-oxobutanoic acid" EXACT RESID-systematic []
-synonym: "HexNAc" RELATED PSI-MS-label []
-synonym: "N4-(2-acetamido-2-deoxy-beta-D-galactopyranosyl)-L-asparagine" EXACT RESID-alternate []
-synonym: "N4-(2-acetylamino-2-deoxy-beta-D-galactopyranosyl)-L-asparagine" EXACT RESID-alternate []
-synonym: "N4-(N-acetylamino)galactosyl-L-asparagine" EXACT RESID-name []
-synonym: "N4-(N-acetylgalactosaminyl)asparagine" EXACT RESID-alternate []
-synonym: "N4-asparagine-beta-N-acetylgalactosaminide" EXACT RESID-alternate []
-synonym: "N4-glycosyl-L-asparagine" EXACT RESID-alternate []
-synonym: "N4-glycosylasparagine" EXACT RESID-alternate []
-synonym: "N4GalNAcAsn" EXACT PSI-MOD-label []
-synonym: "CARBOHYD N-linked (GalNAc) asparagine" EXACT UniProt-feature []
-property_value: DiffAvg "203.19" xsd:float
-property_value: DiffFormula "C 8 H 13 N 1 O 5" xsd:string
-property_value: DiffMono "203.079373" xsd:float
-property_value: Formula "C 12 H 19 N 3 O 7" xsd:string
-property_value: MassAvg "317.30" xsd:float
-property_value: MassMono "317.122300" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0512
-is_a: MOD:00563
-is_a: MOD:01674
-
-[Term]
-id: MOD:00833
-name: N4-glucosyl-L-asparagine
-def: "A protein modification that effectively converts an L-asparagine residue to N4-glucosyl-asparagine." [PubMed:1569073, PubMed:3410849, RESID:AA0421]
-synonym: "(2S)-2-amino-4-(D-glucopyranosyl)amino-4-oxobutanoic acid" EXACT RESID-systematic []
-synonym: "CARBOHYD N-linked (Glc)" EXACT UniProt-feature []
-synonym: "N4-(D-glucopyranosyl)-L-asparagine" EXACT RESID-alternate []
-synonym: "N4-asparagine-glucoside" EXACT RESID-alternate []
-synonym: "N4-glucosyl-L-asparagine" EXACT RESID-name []
-synonym: "N4-glucosylasparagine" EXACT RESID-alternate []
-synonym: "N4-glycosyl-L-asparagine" EXACT RESID-alternate []
-synonym: "N4-glycosylasparagine" EXACT RESID-alternate []
-synonym: "N4GlcAsn" EXACT PSI-MOD-label []
-synonym: "CARBOHYD N-linked (Glc) asparagine" EXACT UniProt-feature []
-property_value: DiffAvg "162.14" xsd:float
-property_value: DiffFormula "C 6 H 10 N 0 O 5" xsd:string
-property_value: DiffMono "162.052823" xsd:float
-property_value: Formula "C 10 H 16 N 2 O 7" xsd:string
-property_value: MassAvg "276.25" xsd:float
-property_value: MassMono "276.095751" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0517
-is_a: MOD:00433
-is_a: MOD:01346
-
-[Term]
-id: MOD:00834
-name: O-(N-acetylamino)fucosyl-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O3-(N-acetamino)fucosylserine." [PubMed:11342554, PubMed:12010970, RESID:AA0422]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-(2-acetamido-2-deoxy-beta-D-fucopyranosyloxy)propanoic acid" EXACT RESID-systematic []
-synonym: "O-(2-acetylamino-2-deoxy-beta-D-fucopyranosyl)-L-serine" EXACT RESID-alternate []
-synonym: "O-(N-acetylamino)fucosyl-L-serine" EXACT RESID-name []
-synonym: "O-(N-acetylfucosaminyl)serine" EXACT RESID-alternate []
-synonym: "O-seryl-beta-N-acetylfucosaminide" EXACT RESID-alternate []
-synonym: "O3-(2-acetamido-2-deoxy-beta-D-fucopyranosyl)-L-serine" EXACT RESID-alternate []
-synonym: "O3-(N-acetylfucosaminyl)serine" EXACT RESID-alternate []
-synonym: "OFucNAcSer" EXACT PSI-MOD-label []
-synonym: "CARBOHYD O-linked (FucNAc) serine" EXACT UniProt-feature []
-property_value: DiffAvg "187.19" xsd:float
-property_value: DiffFormula "C 8 H 13 N 1 O 4" xsd:string
-property_value: DiffMono "187.084458" xsd:float
-property_value: Formula "C 11 H 18 N 2 O 6" xsd:string
-property_value: MassAvg "274.27" xsd:float
-property_value: MassMono "274.116486" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0553
-is_a: MOD:00002
-
-[Term]
-id: MOD:00835
-name: L-3-oxoalanine (Ser)
-def: "A protein modification that effectively converts an L-serine residue to L-oxoalanine." [DeltaMass:349, PubMed:14563551, PubMed:7628016, PubMed:8681943, PubMed:9276974, PubMed:9478923, RESID:AA0185#SER, Unimod:401#S]
-subset: PSI-MOD-slim
-synonym: "(S)-2-amino-3-oxopropanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-3-oxopropionic acid" EXACT RESID-alternate []
-synonym: "C(alpha)-formylglycine" RELATED RESID-misnomer []
-synonym: "dehydrogenated serine residue" RELATED Unimod-description []
-synonym: "Didehydro" RELATED PSI-MS-label []
-synonym: "formylglycine" RELATED Unimod-alternate []
-synonym: "formylglycine (from serine)" EXACT DeltaMass-label []
-synonym: "L-3-oxoalanine" EXACT RESID-name []
-synonym: "L-amino-malonic acid semialdehyde" EXACT RESID-alternate []
-synonym: "L-aminomalonaldehydic acid" EXACT RESID-alternate []
-synonym: "L-serinesemialdehyde" RELATED RESID-misnomer []
-synonym: "MOD_RES 3-oxoalanine (Ser)" EXACT UniProt-feature []
-synonym: "oxoalanine" RELATED Unimod-alternate []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 3 H 3 N 1 O 2" xsd:string
-property_value: MassAvg "85.06" xsd:float
-property_value: MassMono "85.016378" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:401
-is_a: MOD:00916
-is_a: MOD:01169
-is_a: MOD:01888
-
-[Term]
-id: MOD:00836
-name: deuterium disubstituted residue
-def: "A protein modification that effectively substitutes two (2)H deuterium atoms for two (1)H protium atoms." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "D(H)2Res" EXACT PSI-MOD-label []
-is_a: MOD:00786
-
-[Term]
-id: MOD:00837
-name: deuterium tetrasubstituted residue
-def: "A protein modification that effectively substitutes four (2)H deuterium atoms for four (1)H protium atoms." [PubMed:18688235]
-synonym: "D(H)4Res" EXACT PSI-MOD-label []
-is_a: MOD:00786
-
-[Term]
-id: MOD:00838
-name: 3x(2)H labeled L-leucine
-def: "A protein modification that effectively substitutes three (1)H protium atoms with three (2)H deuterium atoms to produce 3x(2)H labeled L-leucine." [Unimod:262#L]
-synonym: "D(H)3Leu" EXACT PSI-MOD-label []
-synonym: "Label:2H(3)" RELATED PSI-MS-label []
-synonym: "Trideuteration" RELATED Unimod-description []
-property_value: DiffAvg "3.02" xsd:float
-property_value: DiffFormula "(1)H -3 (2)H 3" xsd:string
-property_value: DiffMono "3.018830" xsd:float
-property_value: Formula "C 6 (1)H 8 (2)H 3 N 1 O 1" xsd:string
-property_value: MassAvg "116.10" xsd:float
-property_value: MassMono "116.102894" xsd:float
-property_value: Origin "L" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:262
-is_a: MOD:00585
-is_a: MOD:00911
-
-[Term]
-id: MOD:00839
-name: (2)H deuterium labeled residue
-def: "A protein modification that effectively substitutes atoms of particular common isotopes with atoms of or groups containing deuteriumm, (2)H." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:00702
-
-[Term]
-id: MOD:00840
-name: isocyanate reagent derivatized residue
-def: "A protein modification produced by formation of an adduct with an isocyanate compound." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:00848
-
-[Term]
-id: MOD:00841
-name: isothiocyanate reagent derivatized residue
-def: "A protein modification produced by formation of an adduct with an isothiocyanate compound." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:00848
-
-[Term]
-id: MOD:00842
-name: (13)C labeled residue
-def: "A protein modification that effectively substitutes atoms of particular common isotopes with atoms of or groups containing (13)C." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:00702
-
-[Term]
-id: MOD:00843
-name: (15)N labeled residue
-def: "A protein modification that effectively substitutes atoms of particular common isotopes with atoms of or groups containing (15)N." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:00702
-
-[Term]
-id: MOD:00844
-name: (18)O labeled residue
-def: "A protein modification that effectively substitutes atoms of particular common isotopes with atoms of or groups containing (18)O." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:00702
-
-[Term]
-id: MOD:00845
-name: (18)O substituted residue
-def: "A protein modification that effectively substitutes one or more (18)O atoms for (16)O atoms." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:00844
-
-[Term]
-id: MOD:00846
-name: levuglandinyl (prostaglandin H2) adduct
-def: "stub" [PubMed:18688235]
-is_a: MOD:00848
-
-[Term]
-id: MOD:00847
-name: (18)O disubstituted residue
-def: "A protein modification that effectively substitutes two (18)O atom for two (16)O atoms." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:00845
-
-[Term]
-id: MOD:00848
-name: reagent derivatized residue
-def: "A protein modification that is produced by formation of an adduct with a particular compound used as a reagent." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:01156
-
-[Term]
-id: MOD:00849
-name: potassium containing modified residue
-def: "A protein modification that effectively substitutes a potassium atom for a hydrogen atom." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "KRes" EXACT PSI-MOD-label []
-is_a: MOD:00698
-
-[Term]
-id: MOD:00850
-name: unnatural residue
-def: "A protein modification that inserts or replaces a residue with an unnatural residue that is not considered to be derived from a natural residue by some chemical process." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:01157
-
-[Term]
-id: MOD:00851
-name: (18)O labeled deamidated residue
-def: "A protein modification that effectively replaces a carboxamido group with a carboxyl group labeled with (18)O." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00400
-is_a: MOD:00844
-
-[Term]
-id: MOD:00852
-name: 1x(18)O labeled deamidated residue
-def: "A protein modification that effectively replaces a carboxamido group with a carboxyl group labeled with one (18)O." [PubMed:8382902, Unimod:366]
-subset: PSI-MOD-slim
-property_value: DiffAvg "2.99" xsd:float
-property_value: DiffFormula "H -1 N -1 (18)O 1" xsd:string
-property_value: DiffMono "2.988262" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:366
-is_a: MOD:00851
-
-[Term]
-id: MOD:00853
-name: 2x(18)O labeled deamidated residue
-def: "A protein modification that effectively replaces a carboxamido group with a carboxyl group labeled with two (18)O." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: DiffAvg "4.99" xsd:float
-property_value: DiffFormula "H -1 N -1 (16)O -1 (18)O 2" xsd:string
-property_value: DiffMono "4.992508" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00851
-
-[Term]
-id: MOD:00854
-name: protonated L-lysine (L-lysinium) residue
-def: "A protein modification that effectively converts an L-lysine to L-lysinium (protonated L-lysine)." [PubMed:18688235]
-comment: Some sources compute the difference formula for charged, quatenary modified lysine based on protonated lysine rather than neutral lysine residue. In such cases, a comparable difference formula can be calculated based on this derivative.
-subset: PSI-MOD-slim
-property_value: DiffAvg "1.01" xsd:float
-property_value: DiffFormula "C 0 H 1 N 0 O 0" xsd:string
-property_value: DiffMono "1.007276" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 6 H 13 N 2 O 1" xsd:string
-property_value: MassAvg "129.18" xsd:float
-property_value: MassMono "129.102239" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00912
-is_a: MOD:01699
-
-[Term]
-id: MOD:00855
-name: N6,N6,N6-trimethyl-L-lysine (from L-lysinium residue)
-def: "A protein modification that effectively converts an L-lysinium (N6-protonated L-lysine) residue to an N6,N6,N6-trimethyl-L-lysine." [DeltaMass:0, OMSSA:15, PubMed:12590383, PubMed:3145979, PubMed:4304194, PubMed:6778808, PubMed:7093227, PubMed:8453381, Unimod:37#K]
-comment: For amino acids residues, amine trimethylation can effectively only be accomplished with an aminium, protonated primary amino, group. This process accounts only for trimethylation and not protonation. The alternative N6Me3+Lys process (MOD:00083) accounts for both protonation and trimethylation.
-subset: PSI-MOD-slim
-synonym: "N6Me3Lys" EXACT PSI-MOD-label []
-synonym: "trimethylk" EXACT OMSSA-label []
-property_value: DiffAvg "42.08" xsd:float
-property_value: DiffFormula "C 3 H 6 N 0 O 0" xsd:string
-property_value: DiffMono "42.046402" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 9 H 19 N 2 O 1" xsd:string
-property_value: MassAvg "171.26" xsd:float
-property_value: MassMono "171.149190" xsd:float
-property_value: Origin "MOD:00854" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:37
-is_a: MOD:00430
-relationship: derives_from MOD:00854
-
-[Term]
-id: MOD:00856
-name: protonated L-alanine (L-alaninium) residue
-def: "A protein modification that effectively converts an L-alanine residue to an L-alaninium (protonated L-alanine)." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: DiffAvg "1.01" xsd:float
-property_value: DiffFormula "C 0 H 1 N 0 O 0" xsd:string
-property_value: DiffMono "1.007276" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 3 H 7 N 1 O 1" xsd:string
-property_value: MassAvg "73.09" xsd:float
-property_value: MassMono "73.052215" xsd:float
-property_value: Origin "A" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00901
-is_a: MOD:01700
-
-[Term]
-id: MOD:00857
-name: N,N,N-trimethyl-L-alanine (from L-alaninium)
-def: "A protein modification that effectively converts an L-alaninium (protonated L-alanine) residue to an N,N,N-trimethyl-L-alanine." [PubMed:12590383, PubMed:332162, PubMed:3979397, PubMed:6778808, PubMed:7715456, Unimod:37#A]
-comment: For amino acids residues, amine trimethylation can effectively only be accomplished with an aminium, protonated primary amino, group. This process accounts only for trimethylation and not protonation. The alternative N2Me3+Ala process (MOD:00071) accounts for both protonation and trimethylation.
-subset: PSI-MOD-slim
-synonym: "N2Me3Ala" EXACT PSI-MOD-label []
-property_value: DiffAvg "42.08" xsd:float
-property_value: DiffFormula "C 3 H 6 N 0 O 0" xsd:string
-property_value: DiffMono "42.046402" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 6 H 13 N 1 O 1" xsd:string
-property_value: MassAvg "115.18" xsd:float
-property_value: MassMono "115.099165" xsd:float
-property_value: Origin "MOD:00856" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:37
-is_a: MOD:01687
-relationship: derives_from MOD:00856
-
-[Term]
-id: MOD:00858
-name: D-alanine (Ser)
-def: "A protein modification that effectively converts an L-serine residue to D-alanine." [PubMed:7961627, RESID:AA0191#SER]
-synonym: "(R)-2-aminopropanoic acid" EXACT RESID-systematic []
-synonym: "D-Ala(Ser)" EXACT PSI-MOD-label []
-synonym: "D-alanine" EXACT RESID-name []
-synonym: "MOD_RES D-alanine (Ser)" EXACT UniProt-feature []
-property_value: DiffAvg "-16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O -1" xsd:string
-property_value: DiffMono "-15.994915" xsd:float
-property_value: Formula "C 3 H 5 N 1 O 1" xsd:string
-property_value: MassAvg "71.08" xsd:float
-property_value: MassMono "71.037114" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0113
-is_a: MOD:00862
-is_a: MOD:00916
-is_a: MOD:01161
-
-[Term]
-id: MOD:00859
-name: modified residue that can arise from different natural residues
-def: "A protein modification that can be derived from different natural residues by different chemical processes." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:01157
-
-[Term]
-id: MOD:00860
-name: sulfur containing modified residue
-def: "A protein modification that produces an amino acid residue containing an exogenous sulfur atom." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:01156
-
-[Term]
-id: MOD:00861
-name: phosphorus containing modified residue
-def: "A protein modification that produces an amino acid residue containing a phosphorus atom." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:01156
-
-[Term]
-id: MOD:00862
-name: D-alanine
-def: "A protein modification that effectively converts a source amino acid residue to D-alanine." [ChEBI:29949, PubMed:7287302, PubMed:7961627, RESID:AA0191]
-synonym: "(R)-2-aminopropanoic acid" EXACT RESID-systematic []
-synonym: "D-alanine" EXACT RESID-name []
-synonym: "MOD_RES D-alanine (Ala)" EXACT UniProt-feature []
-synonym: "MOD_RES D-alanine (Ser)" EXACT UniProt-feature []
-property_value: Formula "C 3 H 5 N 1 O 1" xsd:string
-property_value: MassAvg "71.08" xsd:float
-property_value: MassMono "71.037114" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00664
-is_a: MOD:00859
-
-[Term]
-id: MOD:00863
-name: D-allo-threonine
-def: "A protein modification that effectively converts an L-threonine residue to D-allo-threonine." [ChEBI:32826, PubMed:18025465, PubMed:6893271, RESID:AA0199]
-synonym: "(2R,3R)-2-amino-3-hydroxybutanoic acid" EXACT RESID-systematic []
-synonym: "D-Thr" EXACT PSI-MOD-label []
-synonym: "D-threonine" EXACT RESID-name []
-synonym: "MOD_RES D-threonine" EXACT UniProt-feature []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 4 H 7 N 1 O 2" xsd:string
-property_value: MassAvg "101.10" xsd:float
-property_value: MassMono "101.047678" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0310
-is_a: MOD:00664
-is_a: MOD:00917
-
-[Term]
-id: MOD:00864
-name: tris-L-cysteinyl L-histidino diiron disulfide
-def: "A protein modification that effectively converts three L-cysteine residues, an L-histidine residue and a two-iron two-sulfur cluster to tris-L-cysteinyl L-histidino diiron disulfide." [PubMed:17766439, PubMed:17766440, RESID:AA0438]
-comment: Cross-link 4.
-synonym: "CDGSH domain iron-sulfur cluster" EXACT RESID-alternate []
-synonym: "di-mu-sulfido(bis-S-cysteinyliron)(S-cysteinyl-N3'-histidinoiron)" EXACT RESID-systematic []
-synonym: "METAL Iron-sulfur (2Fe-2S)" EXACT UniProt-feature []
-synonym: "METAL Iron-sulfur (2Fe-2S); via pros nitrogen" EXACT UniProt-feature []
-synonym: "tris-L-cysteinyl L-histidino diiron disulfide" EXACT RESID-name []
-property_value: DiffAvg "171.78" xsd:float
-property_value: DiffFormula "C 0 Fe 2 H -4 N 0 O 0 S 2" xsd:string
-property_value: DiffMono "171.783814" xsd:float
-property_value: FormalCharge "2-" xsd:string
-property_value: Formula "C 15 Fe 2 H 18 N 6 O 4 S 5" xsd:string
-property_value: MassAvg "618.34" xsd:float
-property_value: MassMono "617.870280" xsd:float
-property_value: Origin "C, C, C, H" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00739
-is_a: MOD:02067
-is_a: MOD:02070
-
-[Term]
-id: MOD:00865
-name: N-aspartyl-glycosylsphingolipidinositolethanolamine
-def: "A protein modification that effectively converts an L-aspartic acid residue to N-aspartyl-glycosylsphingolipidinositolethanolamine." [RESID:AA0439]
-synonym: "GSIAsp" EXACT PSI-MOD-label []
-synonym: "LIPID GPI-like-anchor amidated aspartate" EXACT UniProt-feature []
-synonym: "N-aspartyl-glycosylsphingolipidinositolethanolamine" EXACT RESID-name []
-property_value: DiffAvg "123.05" xsd:float
-property_value: DiffFormula "C 2 H 6 N 1 O 3 P 1" xsd:string
-property_value: DiffMono "123.008530" xsd:float
-property_value: Formula "C 6 H 12 N 2 O 7 P 1" xsd:string
-property_value: MassAvg "255.14" xsd:float
-property_value: MassMono "255.038212" xsd:float
-property_value: Origin "D" xsd:string
-property_value: Source "hypothetical" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0322
-is_a: MOD:00466
-is_a: MOD:00904
-
-[Term]
-id: MOD:00866
-name: dihydroxylated proline
-def: "A protein modification that effectively converts an L-proline residue to one of several dihydroxylated proline residues, such as (2S,3R,4R)-3,4-dihydroxyproline or (2S,3R,4S)-3,4-dihydroxyproline." [PubMed:18688235]
-synonym: "Hy2Pro" EXACT PSI-MOD-label []
-property_value: DiffAvg "32.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 2" xsd:string
-property_value: DiffMono "31.989829" xsd:float
-property_value: Formula "C 5 H 7 N 1 O 3" xsd:string
-property_value: MassAvg "129.12" xsd:float
-property_value: MassMono "129.042593" xsd:float
-property_value: Origin "P" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0024
-is_a: MOD:00428
-is_a: MOD:00678
-
-[Term]
-id: MOD:00867
-name: L-cysteinyl-L-selenocysteine (Cys-Cys)
-def: "A protein modification that effectively cross-links an L-cysteine residue and an L-cysteine converted to an L-selenocysteine residue to form L-cysteinyl-L-selenocystine." [PubMed:10801974, PubMed:12911312, PubMed:17177418, RESID:AA0358#CYS]
-comment: Cross-link 2.
-synonym: "(R,R)-2-amino-3-[3-(2-aminopropanoic acid)sulfanyl]selanylpropanoic acid" EXACT RESID-systematic []
-synonym: "CROSSLNK Cysteinyl-selenocysteine (Cys-Sec)" EXACT UniProt-feature []
-synonym: "CROSSLNK Cysteinyl-selenocysteine (Sec-Cys)" EXACT UniProt-feature []
-synonym: "L-cysteinyl-L-selenocysteine" EXACT RESID-name []
-property_value: DiffAvg "44.90" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0 S -1 Se 1" xsd:string
-property_value: DiffMono "45.928800" xsd:float
-property_value: Formula "C 6 H 8 N 2 O 2 S 1 Se 1" xsd:string
-property_value: MassAvg "251.17" xsd:float
-property_value: MassMono "251.947170" xsd:float
-property_value: Origin "C, C" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:01627
-
-[Term]
-id: MOD:00868
-name: natural, non-standard encoded residue
-def: "A protein modification that inserts or replaces a residue with a natural, non-standard encoded residue, such as N-formyl-L-methionine, L-selenocysteine, or L-pyrrolysine." [PubMed:18688235]
-comment: These are produced exclusively by modification of amino acids acylated to special tRNA before incorporation by ribosomes into proteins. For this reason, they have also been referred to as pre-translational modifications.
-subset: PSI-MOD-slim
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00009
-
-[Term]
-id: MOD:00869
-name: L-alanine residue (Asp)
-def: "A protein modification that effectively converts an L-aspartic acid residue to L-alanine." [PubMed:17138938, RESID:AA0001#ASP]
-comment: This has been reported to occur by a natural process of beta-decarboxylation.
-synonym: "(2S)-2-aminopropanoic acid" EXACT RESID-systematic []
-synonym: "2-aminopropionic acid" EXACT RESID-alternate []
-synonym: "2-azanylpropanoic acid" EXACT RESID-alternate []
-synonym: "alpha-alanine" EXACT RESID-alternate []
-synonym: "alpha-aminopropionic acid" EXACT RESID-alternate []
-synonym: "Asp(Ala)" EXACT PSI-MOD-label []
-synonym: "L-alanine" EXACT RESID-name []
-synonym: "MOD_RES Beta-decarboxylated aspartate" EXACT UniProt-feature []
-property_value: DiffAvg "-44.01" xsd:float
-property_value: DiffFormula "C -1 H 0 N 0 O -2" xsd:string
-property_value: DiffMono "-43.989829" xsd:float
-property_value: Formula "C 3 H 5 N 1 O 1" xsd:string
-property_value: MassAvg "71.08" xsd:float
-property_value: MassMono "71.037114" xsd:float
-property_value: Origin "D" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0314
-is_a: MOD:00904
-is_a: MOD:02088
-
-[Term]
-id: MOD:00870
-name: phenyl isocyanate derivatized residue
-def: "A protein modification produced by formation of an adduct with phenyl isocyanate." [Unimod:411]
-comment: From Unimod with no citation.
-subset: PSI-MOD-slim
-synonym: "phenyl isocyanate" RELATED Unimod-description []
-synonym: "Phenylisocyanate" RELATED PSI-MS-label []
-property_value: DiffAvg "119.12" xsd:float
-property_value: DiffFormula "C 7 H 5 N 1 O 1" xsd:string
-property_value: DiffMono "119.037114" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:411
-is_a: MOD:00840
-
-[Term]
-id: MOD:00871
-name: (2)H5-phenyl isocyanate derivatized residue
-def: "A protein modification produced by formation of an adduct with (2)H5-phenyl isocyanate." [Unimod:412]
-comment: From Unimod with no citation.
-subset: PSI-MOD-slim
-synonym: "d5-phenyl isocyanate" RELATED Unimod-description []
-synonym: "Phenylisocyanate:2H(5)" RELATED PSI-MS-label []
-property_value: DiffAvg "124.07" xsd:float
-property_value: DiffFormula "C 7 (2)H 5 N 1 O 1" xsd:string
-property_value: DiffMono "124.068498" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:412
-relationship: derives_from MOD:00870
-is_a: MOD:01431
-
-[Term]
-id: MOD:00872
-name: L-isoglutamyl monoglutamic acid
-def: "OBSOLETE because redundant and identical to MOD:01970. Remap to MOD:01970." [PubMed:10747868, PubMed:15525938, PubMed:1680872, RESID:AA0202#var, Unimod:450]
-synonym: "Glu" RELATED Unimod-interim []
-synonym: "monoglutamyl" RELATED Unimod-description []
-synonym: "N alpha -(gamma-Glutamyl)-Glu" EXACT DeltaMass-label []
-property_value: DiffAvg "129.12" xsd:float
-property_value: DiffFormula "C 5 H 7 N 1 O 3" xsd:string
-property_value: DiffMono "129.042593" xsd:float
-property_value: Formula "C 10 H 14 N 2 O 6" xsd:string
-property_value: MassAvg "258.23" xsd:float
-property_value: MassMono "258.085186" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "natural" xsd:string
-replaced_by: MOD:01970
-xref: Unimod:450
-is_obsolete: true
-
-[Term]
-id: MOD:00873
-name: L-isoglutamyl diglutamic acid
-def: "A protein modification that effectively converts an L-glutamic acid residue to isoglutamyl glutamyl-glutamic acid, forming an isopeptide bond with a diglutamic acid." [DeltaMass:0, PubMed:10747868, PubMed:1680872, RESID:AA0202#var, Unimod:451]
-synonym: "diglutamyl" RELATED Unimod-description []
-synonym: "GluGlu" RELATED Unimod-interim []
-property_value: DiffAvg "258.23" xsd:float
-property_value: DiffFormula "C 10 H 14 N 2 O 6" xsd:string
-property_value: DiffMono "258.085186" xsd:float
-property_value: Formula "C 15 H 21 N 3 O 9" xsd:string
-property_value: MassAvg "387.35" xsd:float
-property_value: MassMono "387.127779" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:451
-is_a: MOD:00207
-
-[Term]
-id: MOD:00874
-name: L-isoglutamyl triglutamic acid
-def: "A protein modification that effectively converts an L-glutamic acid residue to isoglutamyl glutamyl-glutamyl-glutamic acid, forming an isopeptide bond with a triglutamic acid." [DeltaMass:0, PubMed:10747868, PubMed:1680872, RESID:AA0202#var, Unimod:452]
-comment: From DeltaMass: Average Mass: 388.
-synonym: "GluGluGlu" RELATED Unimod-interim []
-synonym: "N alpha -(gamma-Glutamyl)-Glu3" EXACT DeltaMass-label []
-synonym: "triglutamyl" RELATED Unimod-description []
-property_value: DiffAvg "387.35" xsd:float
-property_value: DiffFormula "C 15 H 21 N 3 O 9" xsd:string
-property_value: DiffMono "387.127779" xsd:float
-property_value: Formula "C 20 H 28 N 4 O 12" xsd:string
-property_value: MassAvg "516.46" xsd:float
-property_value: MassMono "516.170372" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:452
-is_a: MOD:00207
-
-[Term]
-id: MOD:00875
-name: L-isoglutamyl tetraglutamic acid
-def: "A protein modification that effectively converts an L-glutamic acid residue to isoglutamyl glutamyl-glutamyl-glutamyl-glutamic acid, forming an isopeptide bond with a tetraglutamic acid." [PubMed:10747868, PubMed:1680872, RESID:AA0202#var, Unimod:453]
-synonym: "GluGluGluGlu" RELATED Unimod-interim []
-synonym: "tetraglutamyl" RELATED Unimod-description []
-property_value: DiffAvg "516.46" xsd:float
-property_value: DiffFormula "C 20 H 28 N 4 O 12" xsd:string
-property_value: DiffMono "516.170372" xsd:float
-property_value: Formula "C 25 H 35 N 5 O 15" xsd:string
-property_value: MassAvg "645.57" xsd:float
-property_value: MassMono "645.212965" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:453
-is_a: MOD:00207
-
-[Term]
-id: MOD:00876
-name: hexosaminylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of an amino acid residue or of a modifying group with a hexosamine sugar group through a glycosidic bond." [Unimod:454]
-synonym: "HexN" RELATED PSI-MS-label []
-synonym: "Hexosamine" RELATED Unimod-description []
-synonym: "Hexosamines (GalN, GlcN)" EXACT DeltaMass-label []
-property_value: DiffAvg "161.16" xsd:float
-property_value: DiffFormula "C 6 H 11 N 1 O 4" xsd:string
-property_value: DiffMono "161.068808" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:454
-is_a: MOD:00693
-
-[Term]
-id: MOD:00877
-name: imidoester crosslink dimethyl pimelimidate singly attached
-def: "dimethyl pimelimidate modification from Unimod" [Unimod:455, URL:http\://www.piercenet.com/files/0668ss5.pdf]
-synonym: "One end of crosslink attached, one end free" RELATED Unimod-description []
-synonym: "Xlink:DMP-s" RELATED Unimod-interim []
-property_value: DiffAvg "154.21" xsd:float
-property_value: DiffFormula "C 8 H 14 N 2 O 1" xsd:string
-property_value: DiffMono "154.110613" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:455
-is_a: MOD:00848
-
-[Term]
-id: MOD:00878
-name: imidoester crosslink dimethyl pimelimidate doubly attached
-def: "dimethyl pimelimidate modification from Unimod - Mechanism of the reaction of imidoesters with amines" [PubMed:7171546, Unimod:456, URL:http\://dx.doi.org/10.1021/ja00877a017]
-synonym: "Both ends of crosslink attached to same peptide" RELATED Unimod-description []
-synonym: "Xlink:DMP" RELATED Unimod-interim []
-property_value: DiffAvg "122.17" xsd:float
-property_value: DiffFormula "C 7 H 10 N 2" xsd:string
-property_value: DiffMono "122.084398" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:456
-is_a: MOD:00848
-
-[Term]
-id: MOD:00879
-name: naphthalene-2,3-dicarboxaldehyde
-def: "modification from Unimod" [PubMed:2081203, Unimod:457]
-synonym: "naphthalene-2,3-dicarboxaldehyde" RELATED Unimod-description []
-synonym: "NDA" RELATED Unimod-interim []
-property_value: DiffAvg "175.19" xsd:float
-property_value: DiffFormula "C 13 H 5 N 1" xsd:string
-property_value: DiffMono "175.042199" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:457
-is_a: MOD:00848
-
-[Term]
-id: MOD:00880
-name: 6x(13)C labeled 4-sulfophenyl isothiocyanate derivatized residue
-def: "A protein modification produced by formation of an adduct with 6x(13)C labeled 4-sulfophenyl isothiocyanate." [PubMed:15536630, PubMed:16526082, Unimod:464]
-synonym: "4-sulfophenyl isothiocyanate (Heavy C13)" RELATED Unimod-description []
-synonym: "SPITC:13C(6)" RELATED PSI-MS-label []
-property_value: DiffAvg "220.99" xsd:float
-property_value: DiffFormula "(12)C 1 (13)C 6 H 5 N 1 O 3 S 2" xsd:string
-property_value: DiffMono "220.991214" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:464
-relationship: derives_from MOD:00584
-is_a: MOD:01428
-
-[Term]
-id: MOD:00881
-name: N-reductive amination-D
-def: "OBSOLETE because Unimod entry 465 megerd with 199. Remap to MOD:00552 DiMethyl-CH2D." [PubMed:9252331, Unimod:465]
-property_value: DiffAvg "32.06" xsd:float
-property_value: DiffFormula "C 2 (2)H 4" xsd:string
-property_value: DiffMono "32.056407" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-replaced_by: MOD:00552
-xref: Unimod:465
-is_obsolete: true
-
-[Term]
-id: MOD:00882
-name: S-(2-aminoethyl)cysteine (Ser)
-def: "A protein modification that effectively converts an L-serine residue to S-(2-aminoethyl)cysteine." [DeltaMass:171, PubMed:12923550, Unimod:472#S]
-comment: From DeltaMass: Average Mass: 146 Abbreviation:-AECys_ Formula:C5H10O2N1S1 Monoisotopic Mass Change:146.051 Average Mass Change:146.214 References:PE Sciex.
-synonym: "AEC-MAEC" RELATED Unimod-interim []
-synonym: "Aminoethyl Cysteinyl (AECys)" EXACT DeltaMass-label []
-synonym: "aminoethylcysteine" RELATED Unimod-description []
-property_value: DiffAvg "59.13" xsd:float
-property_value: DiffFormula "C 2 H 5 N 1 O -1 S 1" xsd:string
-property_value: DiffMono "59.019356" xsd:float
-property_value: Formula "C 5 H 10 N 2 O 1 S 1" xsd:string
-property_value: MassAvg "146.21" xsd:float
-property_value: MassMono "146.051384" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:472
-is_a: MOD:00916
-
-[Term]
-id: MOD:00883
-name: C1-amidated residue
-def: "A protein modification that effectively replaces a 1-carboxyl group (usually referred to as the alpha-carboxyl) with a carboxamido group." [DeltaMass:0, OMSSA:25, Unimod:2]
-comment: The normal biological process involves formation of an amide of an amino acid residue in a peptide sequence where it is followed by a glycine and two basic residues, either arginine or lysine, although in some taxa only one basic residue is required. The peptide is cleaved after the basic residues, glycine is oxidized to hydroxyglycine, which decomposes to release a carboxamide C-terminal [JSG].
-subset: PSI-MOD-slim
-synonym: "alpha-amidated residue" EXACT PSI-MOD-alternate []
-synonym: "Amidated" RELATED PSI-MS-label []
-synonym: "Amidation" RELATED Unimod-description []
-synonym: "Amide formation (C terminus)" EXACT DeltaMass-label []
-synonym: "ctermamide" EXACT OMSSA-label []
-synonym: "ResN" EXACT PSI-MOD-label []
-property_value: DiffAvg "-0.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 1 O -1" xsd:string
-property_value: DiffMono "-0.984016" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: Unimod:2
-is_a: MOD:00674
-
-[Term]
-id: MOD:00884
-name: S-aminoethylcysteine (Cys)
-def: "A protein modification that effectively converts an L-cysteine residue to S-2-aminoethylcysteine." [PubMed:1175632, PubMed:18688235]
-comment: This modified residue is a chemical isolog of L-lysine for trypsin hydolysis produced from L-cysteine by aziridine.
-subset: PSI-MOD-slim
-synonym: "4-thialysine" EXACT PSI-MOD-alternate []
-synonym: "L-cysteine aziridine adduct" EXACT PSI-MOD-alternate []
-synonym: "S-(2-aminoethyl)-L-cysteine" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "43.07" xsd:float
-property_value: DiffFormula "C 2 H 5 N 1 O 0 S 0" xsd:string
-property_value: DiffMono "43.042199" xsd:float
-property_value: Formula "C 5 H 10 N 2 O 1 S 1" xsd:string
-property_value: MassAvg "146.21" xsd:float
-property_value: MassMono "146.051384" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-is_a: MOD:00905
-
-[Term]
-id: MOD:00885
-name: ester crosslinked residues
-def: "A protein modification that crosslinks two residues by formation of an ester bond." [PubMed:18688235]
-is_a: MOD:00033
-
-[Term]
-id: MOD:00886
-name: 6'-chloro-L-tryptophan
-def: "A protein modification that effectively converts an L-tryptophan residue to 6'-chloro-L-tryptophan." [PubMed:9033387, RESID:AA0180, Unimod:936#W]
-comment: The Unimod:340 cross-reference to RESID:AA0180 is incorrect. RESID:AA0180 should be cross-referenced by Unimod:936 [JSG].
-synonym: "(2S)-2-amino-3-(6-chloro-1H-indol-3-yl)propanoic acid" EXACT RESID-systematic []
-synonym: "6'-chloro-L-tryptophan" EXACT RESID-name []
-synonym: "6'-ClTrp" EXACT PSI-MOD-label []
-synonym: "MOD_RES 6'-chlorotryptophan" EXACT UniProt-feature []
-property_value: DiffAvg "34.44" xsd:float
-property_value: DiffFormula "C 0 Cl 1 H -1 N 0 O 0" xsd:string
-property_value: DiffMono "33.961028" xsd:float
-property_value: Formula "C 11 Cl 1 H 9 N 2 O 1" xsd:string
-property_value: MassAvg "220.66" xsd:float
-property_value: MassMono "220.040341" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:936
-xref: uniprot.ptm:PTM-0052
-is_a: MOD:01913
-
-[Term]
-id: MOD:00887
-name: methylated aspartic acid
-def: "A protein modification that effectively converts an L-aspartic acid residue to a methylated aspartic acid, such as aspartic acid 4-methyl ester." [PubMed:18688235]
-is_a: MOD:00427
-is_a: MOD:00904
-
-[Term]
-id: MOD:00888
-name: protonated L-proline (L-prolinium) residue
-def: "A protein modification that effectively converts an L-proline to an L-prolinium (protonated L-proline)." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: DiffAvg "1.01" xsd:float
-property_value: DiffFormula "C 0 H 1 N 0 O 0" xsd:string
-property_value: DiffMono "1.007276" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 5 H 9 N 1 O 1" xsd:string
-property_value: MassAvg "99.13" xsd:float
-property_value: MassMono "99.067865" xsd:float
-property_value: Origin "P" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00915
-is_a: MOD:01700
-
-[Term]
-id: MOD:00889
-name: N,N-dimethyl-L-proline (from L-prolinium)
-def: "A protein modification that effectively converts an L-prolinium (charged L-proline) residue to N,N-dimethyl-L-proline." [Unimod:36#P]
-subset: PSI-MOD-slim
-property_value: DiffAvg "28.05" xsd:float
-property_value: DiffFormula "C 2 H 4 N 0 O 0" xsd:string
-property_value: DiffMono "28.030752" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 7 H 13 N 1 O 1" xsd:string
-property_value: MassAvg "127.19" xsd:float
-property_value: MassMono "127.099165" xsd:float
-property_value: Origin "MOD:00888" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:36
-relationship: derives_from MOD:00075
-relationship: derives_from MOD:00888
-is_a: MOD:00712
-is_a: MOD:00710
-is_a: MOD:01686
-
-[Term]
-id: MOD:00890
-name: phosphorylated L-histidine
-def: "A protein modification that effectively converts an L-histidine residue to a phosphorylated L-histidine, such as pros-phosphohistidine, or tele-phosphohistidine." [OMSSA:192, Unimod:21#H]
-subset: PSI-MOD-slim
-synonym: "mod192" EXACT OMSSA-label []
-synonym: "NPhosHis" EXACT PSI-MOD-label []
-synonym: "Phospho" RELATED PSI-MS-label []
-synonym: "phosphohistidine" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "79.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 0 O 3 P 1" xsd:string
-property_value: DiffMono "79.966331" xsd:float
-property_value: Formula "C 6 H 8 N 3 O 4 P 1" xsd:string
-property_value: MassAvg "217.12" xsd:float
-property_value: MassMono "217.025242" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:21
-xref: uniprot.ptm:PTM-0252
-is_a: MOD:00909
-is_a: MOD:01456
-
-[Term]
-id: MOD:00891
-name: D-serine
-def: "A protein modification that effectively converts a source amino acid residue to D-serine." [ChEBI:29998, PubMed:6893271, PubMed:7973665, RESID:AA0195]
-synonym: "(R)-2-amino-3-hydroxypropanoic acid" EXACT RESID-systematic []
-synonym: "D-Ser" EXACT PSI-MOD-label []
-synonym: "D-serine" EXACT RESID-name []
-property_value: Formula "C 3 H 5 N 1 O 2" xsd:string
-property_value: MassAvg "87.08" xsd:float
-property_value: MassMono "87.032028" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00664
-is_a: MOD:00859
-
-[Term]
-id: MOD:00892
-name: D-serine (Cys)
-def: "A protein modification that effectively converts an L-cysteine residue to D-serine." [PubMed:18025465, PubMed:6893271, RESID:AA0195#CYS]
-synonym: "(R)-2-amino-3-hydroxypropanoic acid" EXACT RESID-systematic []
-synonym: "D-serine" EXACT RESID-name []
-synonym: "MOD_RES D-serine (Cys)" EXACT UniProt-feature []
-property_value: DiffAvg "-16.06" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1 S -1" xsd:string
-property_value: DiffMono "-15.977156" xsd:float
-property_value: Formula "C 3 H 5 N 1 O 2" xsd:string
-property_value: MassAvg "87.08" xsd:float
-property_value: MassMono "87.032028" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0309
-is_a: MOD:00891
-is_a: MOD:00905
-
-[Term]
-id: MOD:00893
-name: residues isobaric at 128.0-128.1
-def: "Natural or modified residues with a mass of 128.0-128.1 Da." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:00616
-
-[Term]
-id: MOD:00894
-name: residues isobaric at 128.058578 Da
-def: "Natural or modified resiues with a mass of 128.058578 Da." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:00569
-is_a: MOD:00893
-
-[Term]
-id: MOD:00895
-name: FAD modified residue
-def: "A protein modification that effectively results from forming an adduct with a compound containing a flavin adenine dinucleotide (FAD) group." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "FADRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "783.54" xsd:float
-property_value: DiffFormula "C 27 H 31 N 9 O 15 P 2" xsd:string
-property_value: DiffMono "783.141485" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00697
-is_a: MOD:00861
-
-[Term]
-id: MOD:00896
-name: FMN modified residue
-def: "A protein modification that effectively results from forming an adduct with a compound containing a riboflavin phosphate (flavin mononucleotide, FMN) group." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "FMNRes" EXACT PSI-MOD-label []
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00697
-is_a: MOD:00861
-
-[Term]
-id: MOD:00897
-name: N-acetyl-S-archeol-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to N-acetyl-S-archeol-L-cysteine." [RESID:AA0043#var, RESID:AA0223#var]
-property_value: DiffAvg "677.20" xsd:float
-property_value: DiffFormula "C 45 H 88 N 0 O 3 S 0" xsd:string
-property_value: DiffMono "676.673347" xsd:float
-property_value: Formula "C 48 H 93 N 1 O 4 S 1" xsd:string
-property_value: MassAvg "780.34" xsd:float
-property_value: MassMono "779.682531" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00905
-relationship: has_functional_parent MOD:00052
-relationship: has_functional_parent MOD:00228
-
-[Term]
-id: MOD:00898
-name: S-(sn-1-2-oleoyl-3-palmitoyl-glycerol)cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-(sn-1-2-oleoyl-3-palmitoyl-glycerol)cysteine." [PubMed:10896212, PubMed:4575979, PubMed:9056182, RESID:AA0107#var, Unimod:377]
-comment: Incidental to RESID:AA0060.
-synonym: "Diacylglycerol" RELATED PSI-MS-label []
-synonym: "diacylglycerol" RELATED Unimod-description []
-property_value: DiffAvg "576.95" xsd:float
-property_value: DiffFormula "C 37 H 68 N 0 O 4 S 0" xsd:string
-property_value: DiffMono "576.511761" xsd:float
-property_value: Formula "C 40 H 73 N 1 O 5 S 1" xsd:string
-property_value: MassAvg "680.09" xsd:float
-property_value: MassMono "679.520945" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:377
-is_a: MOD:00116
-
-[Term]
-id: MOD:00899
-name: N-palmitoyl-S-diacylglycerol-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to N-palmitoyl-S-diacylglycerol-L-cysteine." [RESID:AA0069#var, RESID:AA0107#var]
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00905
-relationship: has_functional_parent MOD:00069
-relationship: has_functional_parent MOD:00116
-
-[Term]
-id: MOD:00900
-name: N-palmitoyl-S-(sn-1-2-oleoyl-3-palmitoyl-glycerol)cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to N-palmitoyl-S-(sn-1-2-oleoyl-3-palmitoyl-glycerol)cysteine." [PubMed:18688235]
-synonym: "(R)-2-hexadecanoylamino-3-[(S)-2-((Z)-9-octadecenoyloxy)-3-(hexadecanoyloxy)propyl]sulfanylpropanoic acid" EXACT PSI-MOD-alternate []
-synonym: "2-hexadecanoylamino-3-[(S)-2-((Z)-9-octadecenoyloxy)-3-(hexadecanoyloxy)propyl]thiopropanoic acid" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "815.36" xsd:float
-property_value: DiffFormula "C 53 H 98 N 0 O 5 S 0" xsd:string
-property_value: DiffMono "814.741426" xsd:float
-property_value: Formula "C 56 H 103 N 1 O 6 S 1" xsd:string
-property_value: MassAvg "918.50" xsd:float
-property_value: MassMono "917.750611" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00899
-relationship: has_functional_parent MOD:00069
-relationship: has_functional_parent MOD:00898
-
-[Term]
-id: MOD:00901
-name: modified L-alanine residue
-def: "A protein modification that modifies an L-alanine." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "ModAla" EXACT PSI-MOD-label []
-property_value: Origin "A" xsd:string
-is_a: MOD:01157
-
-[Term]
-id: MOD:00902
-name: modified L-arginine residue
-def: "A protein modification that modifies an L-arginine residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "ModArg" EXACT PSI-MOD-label []
-property_value: Origin "R" xsd:string
-is_a: MOD:01157
-
-[Term]
-id: MOD:00903
-name: modified L-asparagine residue
-def: "A protein modification that modifies an L-asparagine residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "ModAsn" EXACT PSI-MOD-label []
-property_value: Origin "N" xsd:string
-is_a: MOD:01157
-
-[Term]
-id: MOD:00904
-name: modified L-aspartic acid residue
-def: "A protein modification that modifies an L-aspartic acid residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "ModAsp" EXACT PSI-MOD-label []
-property_value: Origin "D" xsd:string
-is_a: MOD:01157
-
-[Term]
-id: MOD:00905
-name: modified L-cysteine residue
-def: "A protein modification that modifies an L-cysteine residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "ModCys" EXACT PSI-MOD-label []
-property_value: Origin "C" xsd:string
-is_a: MOD:01157
-
-[Term]
-id: MOD:00906
-name: modified L-glutamic acid residue
-def: "A protein modification that modifies an L-glutamic acid residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "ModGlu" EXACT PSI-MOD-label []
-property_value: Origin "E" xsd:string
-is_a: MOD:01157
-
-[Term]
-id: MOD:00907
-name: modified L-glutamine residue
-def: "A protein modification that modifies an L-glutamine residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "ModGln" EXACT PSI-MOD-label []
-property_value: Origin "Q" xsd:string
-is_a: MOD:01157
-
-[Term]
-id: MOD:00908
-name: modified glycine residue
-def: "A protein modification that modifies a glycine residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "ModGly" EXACT PSI-MOD-label []
-property_value: Origin "G" xsd:string
-is_a: MOD:01157
-
-[Term]
-id: MOD:00909
-name: modified L-histidine residue
-def: "A protein modification that modifies an L-histidine residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "ModHis" EXACT PSI-MOD-label []
-property_value: Origin "H" xsd:string
-is_a: MOD:01157
-
-[Term]
-id: MOD:00910
-name: modified L-isoleucine residue
-def: "A protein modification that modifies an L-isoleucine residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "ModIle" EXACT PSI-MOD-label []
-property_value: Origin "I" xsd:string
-is_a: MOD:01157
-
-[Term]
-id: MOD:00911
-name: modified L-leucine residue
-def: "A protein modification that modifies an L-leucine residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "ModLeu" EXACT PSI-MOD-label []
-property_value: Origin "L" xsd:string
-is_a: MOD:01157
-
-[Term]
-id: MOD:00912
-name: modified L-lysine residue
-def: "A protein modification that modifies an L-lysine residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "ModLys" EXACT PSI-MOD-label []
-property_value: Origin "K" xsd:string
-is_a: MOD:01157
-
-[Term]
-id: MOD:00913
-name: modified L-methionine residue
-def: "A protein modification that modifies an L-methionine residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "ModMet" EXACT PSI-MOD-label []
-property_value: Origin "M" xsd:string
-is_a: MOD:01157
-
-[Term]
-id: MOD:00914
-name: modified L-phenylalanine residue
-def: "A protein modification that modifies an L-phenylalanine residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "ModPhe" EXACT PSI-MOD-label []
-property_value: Origin "F" xsd:string
-is_a: MOD:01157
-
-[Term]
-id: MOD:00915
-name: modified L-proline residue
-def: "A protein modification that modifies an L-proline residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "ModPro" EXACT PSI-MOD-label []
-property_value: Origin "P" xsd:string
-is_a: MOD:01157
-
-[Term]
-id: MOD:00916
-name: modified L-serine residue
-def: "A protein modification that modifies an L-serine residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "ModSer" EXACT PSI-MOD-label []
-property_value: Origin "S" xsd:string
-is_a: MOD:01157
-
-[Term]
-id: MOD:00917
-name: modified L-threonine residue
-def: "A protein modification that modifies an L-threonine residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "ModThr" EXACT PSI-MOD-label []
-property_value: Origin "T" xsd:string
-is_a: MOD:01157
-
-[Term]
-id: MOD:00918
-name: modified L-tryptophan residue
-def: "A protein modification that modifies an L-tryptophan residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "ModTrp" EXACT PSI-MOD-label []
-property_value: Origin "W" xsd:string
-is_a: MOD:01157
-
-[Term]
-id: MOD:00919
-name: modified L-tyrosine residue
-def: "A protein modification that modifies an L-tyrosine residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "ModTyr" EXACT PSI-MOD-label []
-property_value: Origin "Y" xsd:string
-is_a: MOD:01157
-
-[Term]
-id: MOD:00920
-name: modified L-valine residue
-def: "A protein modification that modifies an L-valine residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "ModVal" EXACT PSI-MOD-label []
-property_value: Origin "V" xsd:string
-is_a: MOD:01157
-
-[Term]
-id: MOD:00921
-name: new uncategorized Unimod entries
-def: "New uncategorized Unimod. OBSOLETE because organizational use is no longer required." [PubMed:18688235]
-is_obsolete: true
-
-[Term]
-id: MOD:00922
-name: Cy3 CyDye DIGE Fluor saturation dye
-def: "modification from Unimod Chemical derivative" [Unimod:494]
-synonym: "Cy3 CyDye DIGE Fluor saturation dye" RELATED Unimod-description []
-synonym: "CyDye-Cy3" RELATED Unimod-interim []
-property_value: DiffAvg "672.84" xsd:float
-property_value: DiffFormula "C 37 H 44 N 4 O 6 S 1" xsd:string
-property_value: DiffMono "672.298156" xsd:float
-property_value: Formula "C 40 H 49 N 5 O 7 S 2" xsd:string
-property_value: MassAvg "775.98" xsd:float
-property_value: MassMono "775.307341" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:494
-is_a: MOD:00848
-is_a: MOD:00905
-
-[Term]
-id: MOD:00923
-name: Cy5 CyDye DIGE Fluor saturation dye
-def: "modification from Unimod Chemical derivative" [Unimod:495]
-synonym: "Cy5 CyDye DIGE Fluor saturation dye" RELATED Unimod-description []
-synonym: "CyDye-Cy5" RELATED Unimod-interim []
-property_value: DiffAvg "684.85" xsd:float
-property_value: DiffFormula "C 38 H 44 N 4 O 6 S 1" xsd:string
-property_value: DiffMono "684.298156" xsd:float
-property_value: Formula "C 41 H 49 N 5 O 7 S 2" xsd:string
-property_value: MassAvg "787.99" xsd:float
-property_value: MassMono "787.307341" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:495
-is_a: MOD:00848
-is_a: MOD:00905
-
-[Term]
-id: MOD:00924
-name: N6-(L-threonyl)-L-lysine
-def: "A protein modification that effectively crosslinks an L-lysine residue and an L-threonine residue by an isopeptide bond to form N6-(L-threonyl)-L-lysine." [PubMed:18063774, RESID:AA0440]
-comment: Cross-link 2.
-synonym: "(2S)-2-amino-6-([(2S,3R)-2-amino-3-hydroxybutanoyl]amino)hexanoic acid" EXACT RESID-systematic []
-synonym: "N6-(L-threonyl)-L-lysine" EXACT RESID-name []
-synonym: "N6-threonyl-lysine" EXACT RESID-alternate []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 10 H 18 N 3 O 3" xsd:string
-property_value: MassAvg "228.27" xsd:float
-property_value: MassMono "228.134816" xsd:float
-property_value: Origin "K, T" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0326
-is_a: MOD:00688
-is_a: MOD:02056
-is_a: MOD:02051
-is_a: MOD:00954
-is_a: MOD:01875
-
-[Term]
-id: MOD:00925
-name: heptosylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of an amino acid residue or of a modifying group with a heptose sugar group through a glycosidic bond." [Unimod:490]
-comment: From Unimod with no citation [JSG].
-synonym: "Hep" RELATED PSI-MS-label []
-synonym: "Heptose" RELATED Unimod-description []
-property_value: DiffAvg "192.17" xsd:float
-property_value: DiffFormula "C 7 H 12 O 6" xsd:string
-property_value: DiffMono "192.063388" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:490
-is_a: MOD:00693
-
-[Term]
-id: MOD:00926
-name: Bisphenol A diglycidyl ether derivative
-def: "Modification from Unimod Non-standard residue. OBSOLETE because not an amino acid modification. From Unimod not an approved entry." [PubMed:11225353, Unimod:493]
-synonym: "BADGE" RELATED Unimod-interim []
-synonym: "Bisphenol A diglycidyl ether derivative" RELATED Unimod-description []
-property_value: DiffAvg "340.42" xsd:float
-property_value: DiffFormula "C 21 H 24 O 4" xsd:string
-property_value: DiffMono "340.167459" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:493
-is_obsolete: true
-
-[Term]
-id: MOD:00927
-name: 2x(13)C,4x(2)H labeled dimethylated residue
-def: "A protein modification that effectively replaces two hydrogen atoms of a residue containing common isotopes with two (13)C,3x(2)H labeled methyl groups to form a 2x(13)C,6x(2)H labeled dimethylated residue." [PubMed:16335955, PubMed:3802193, Unimod:510]
-synonym: "DiMethyl-C13HD2" RELATED Unimod-description []
-synonym: "Dimethyl:2H(4)13C(2)" RELATED PSI-MS-label []
-property_value: DiffAvg "34.06" xsd:float
-property_value: DiffFormula "(13)C 2 (2)H 4" xsd:string
-property_value: DiffMono "34.063117" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:510
-is_a: MOD:00839
-is_a: MOD:00842
-
-[Term]
-id: MOD:00928
-name: [3-(2,5)-dioxopyrrolidin-1-yloxycarbonyl)-propyl]dimethyloctylammonium
-def: "modification from Unimod Chemical derivative" [PubMed:16771548, Unimod:513]
-comment: Should have children for K and X-N-term [JSG].
-synonym: "[3-(2,5)-Dioxopyrrolidin-1-yloxycarbonyl)-propyl]dimethyloctylammonium" RELATED Unimod-description []
-synonym: "C8-QAT" RELATED Unimod-interim []
-property_value: DiffAvg "227.39" xsd:float
-property_value: DiffFormula "C 14 H 29 N 1 O 1" xsd:string
-property_value: DiffMono "227.224915" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:513
-is_a: MOD:00848
-
-[Term]
-id: MOD:00929
-name: lactose glycated lysine
-def: "A modification produced in a non-enzymatic reaction between a lactose carbonyl group and an L-lysine to form a Schiff-base or an Amadori ketosamine lysine adduct." [PubMed:9606156, Unimod:512]
-comment: The term lactosylation used with this meaning is a misnomer [JSG].
-synonym: "Hex(2)" RELATED Unimod-interim []
-synonym: "Lactosylation" RELATED Unimod-description []
-synonym: "CARBOHYD N-linked (Lac) (glycation) lysine" EXACT UniProt-feature []
-property_value: DiffAvg "342.30" xsd:float
-property_value: DiffFormula "C 12 H 22 O 11" xsd:string
-property_value: DiffMono "342.116212" xsd:float
-property_value: Formula "C 18 H 34 N 2 O 12" xsd:string
-property_value: MassAvg "470.47" xsd:float
-property_value: MassMono "470.211175" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:512
-xref: uniprot.ptm:PTM-0511
-is_a: MOD:00767
-is_a: MOD:00912
-
-[Term]
-id: MOD:00930
-name: propyl-NAG tyrosine adduct
-def: "tyrosine adduct with substrate analog inhibitor 1,2-dideoxy-2'-methyl-alpha-D-glucopyranoso-[2,1-d]-Delta2'-thiazoline." [PubMed:15795231, Unimod:514]
-property_value: DiffAvg "232.27" xsd:float
-property_value: DiffFormula "C 9 H 14 N 1 O 4 S 1" xsd:string
-property_value: DiffMono "232.064354" xsd:float
-property_value: Formula "C 18 H 23 N 2 O 6 S 1" xsd:string
-property_value: MassAvg "395.45" xsd:float
-property_value: MassMono "395.127682" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:514
-is_a: MOD:00848
-is_a: MOD:00919
-
-[Term]
-id: MOD:00931
-name: Michael addition of t-butyl hydroxylated BHT (BHTOH) to C, H or K
-def: "modification from Unimod Other - BHTOH is formed upon metabolism of BHT with P450 enzymes. The BHTOH is further metabolized to its quinone methide (electrophile) which reacts with -SH and -NH2 groups" [PubMed:11085420, Unimod:498]
-synonym: "BHTOH" RELATED Unimod-interim []
-synonym: "Michael addition of t-butyl hydroxylated BHT (BHTOH) to C, H or K" RELATED Unimod-description []
-property_value: DiffAvg "234.34" xsd:float
-property_value: DiffFormula "C 15 H 22 O 2" xsd:string
-property_value: DiffMono "234.161980" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:498
-is_a: MOD:00848
-
-[Term]
-id: MOD:00932
-name: IDBEST tag for quantitation
-def: "modification from Unimod Isotopic label" [PubMed:11821862, Unimod:499]
-synonym: "Heavy IDBEST tag for quantitation" RELATED Unimod-description []
-synonym: "IGBP:13C(2)" RELATED PSI-MS-label []
-property_value: DiffAvg "298.02" xsd:float
-property_value: DiffFormula "Br 1 (12)C 10 (13)C 2 H 13 N 2 O 2" xsd:string
-property_value: DiffMono "298.022749" xsd:float
-property_value: Formula "Br 1 (12)C 13 (13)C 2 H 18 N 3 O 3 S 1" xsd:string
-property_value: MassAvg "401.03" xsd:float
-property_value: MassMono "401.031934" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:499
-is_a: MOD:00905
-is_a: MOD:01428
-
-[Term]
-id: MOD:00933
-name: methylglyoxal arginine adduct (+54 amu)
-def: "modification from Unimod Chemical derivative - 5-hydro-5-methylimidazol-4-one, arginine methylglyoxal arginine adduct (+54 amu)" [Unimod:319#R]
-comment: Ref. Uchida K, Sakai K, Itakura K, Osawa T, Toyokuni S. 1977. Protein modification by lipid peroxidation products: formation of malondialdehyde-derived N(epsilon)-(2-propenol)lysine in proteins. Arch Biochem Biophys. 346(1):45-52.
-synonym: "Delta:H(2)C(3)O(1)" RELATED PSI-MS-label []
-synonym: "MDA adduct +54" RELATED Unimod-description []
-property_value: DiffAvg "54.05" xsd:float
-property_value: DiffFormula "C 3 H 2 O 1" xsd:string
-property_value: DiffMono "54.010565" xsd:float
-property_value: Formula "C 9 H 14 N 4 O 2" xsd:string
-property_value: MassAvg "210.24" xsd:float
-property_value: MassMono "210.111676" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:319
-is_a: MOD:00630
-is_a: MOD:00902
-
-[Term]
-id: MOD:00934
-name: Levuglandinyl - arginine hydroxylactam adduct
-def: "modification from Unimod Post-translational" [Unimod:506]
-synonym: "Levuglandinyl - arginine hydroxylactam adduct" RELATED Unimod-description []
-synonym: "LG-Hlactam-R" RELATED Unimod-interim []
-property_value: DiffAvg "306.40" xsd:float
-property_value: DiffFormula "C 19 H 26 N -2 O 5" xsd:string
-property_value: DiffMono "306.171876" xsd:float
-property_value: Formula "C 25 H 38 N 2 O 6" xsd:string
-property_value: MassAvg "462.59" xsd:float
-property_value: MassMono "462.272987" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:506
-is_a: MOD:00846
-is_a: MOD:00902
-
-[Term]
-id: MOD:00935
-name: methionine oxidation with neutral loss of 64 Da
-def: "Oxidation of methionine to methionine sulfoxide with neutral loss of CH3SOH." [PubMed:18688235, PubMed:9004526]
-comment: Originally created from Unimod:507 that was later deleted.
-property_value: DiffAvg "-64.10" xsd:float
-property_value: DiffFormula "C -1 H -4 N 0 O -1 S -1" xsd:string
-property_value: DiffMono "-63.998286" xsd:float
-property_value: Formula "C 4 H 5 N 1 O 1 S 0" xsd:string
-property_value: MassAvg "83.09" xsd:float
-property_value: MassMono "83.037114" xsd:float
-property_value: Origin "M" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00431
-is_a: MOD:00913
-
-[Term]
-id: MOD:00936
-name: Levuglandinyl - hydroxylactam adduct, K and N-term
-def: "modification from Unimod Post-translational" [Unimod:504]
-synonym: "Levuglandinyl - lysine hydroxylactam adduct" RELATED Unimod-description []
-synonym: "LG-Hlactam-K" RELATED Unimod-interim []
-property_value: DiffAvg "348.44" xsd:float
-property_value: DiffFormula "C 20 H 28 O 5" xsd:string
-property_value: DiffMono "348.193674" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:504
-is_a: MOD:00846
-
-[Term]
-id: MOD:00937
-name: Levuglandinyl - arginine lactam adduct
-def: "modification from Unimod Post-translational" [Unimod:505]
-synonym: "Levuglandinyl - arginine lactam adduct" RELATED Unimod-description []
-synonym: "LG-lactam-R" RELATED Unimod-interim []
-property_value: DiffAvg "290.40" xsd:float
-property_value: DiffFormula "C 19 H 26 N -2 O 4" xsd:string
-property_value: DiffMono "290.176961" xsd:float
-property_value: Formula "C 25 H 38 N 2 O 5" xsd:string
-property_value: MassAvg "446.59" xsd:float
-property_value: MassMono "446.278072" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:505
-is_a: MOD:00846
-is_a: MOD:00902
-
-[Term]
-id: MOD:00938
-name: Levuglandinyl - lactam adduct, K and N-term
-def: "modification from Unimod Post-translational" [PubMed:12590383, Unimod:503]
-synonym: "Levuglandinyl - lysine lactam adduct" RELATED Unimod-description []
-synonym: "LG-lactam-K" RELATED Unimod-interim []
-property_value: DiffAvg "332.44" xsd:float
-property_value: DiffFormula "C 20 H 28 O 4" xsd:string
-property_value: DiffMono "332.198759" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:503
-is_a: MOD:00846
-
-[Term]
-id: MOD:00939
-name: hydrolyzed N-methylmaleimide cysteine adduct
-def: "modification from Unimod Chemical derivative" [Unimod:500]
-synonym: "Nmethylmaleimide+water" RELATED Unimod-interim []
-synonym: "Nmethylmaleimidehydrolysis" RELATED Unimod-description []
-property_value: DiffAvg "129.12" xsd:float
-property_value: DiffFormula "C 5 H 7 N 1 O 3" xsd:string
-property_value: DiffMono "129.042593" xsd:float
-property_value: Formula "C 8 H 12 N 2 O 4 S 1" xsd:string
-property_value: MassAvg "232.25" xsd:float
-property_value: MassMono "232.051778" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:500
-is_a: MOD:00848
-is_a: MOD:00905
-
-[Term]
-id: MOD:00940
-name: 3-methyl-2-pyridyl isocyanate derivatized residue
-def: "A protein modification produced by formation of an adduct with 3-methyl-2-pyridyl isocyanate." [PubMed:11078590, Unimod:501]
-synonym: "3-methyl-2-pyridyl isocyanate" RELATED Unimod-description []
-synonym: "PyMIC" RELATED Unimod-interim []
-property_value: DiffAvg "134.14" xsd:float
-property_value: DiffFormula "C 7 H 6 N 2 O 1" xsd:string
-property_value: DiffMono "134.048013" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:501
-is_a: MOD:00840
-
-[Term]
-id: MOD:00941
-name: dehydropyrrolizidine alkaloid (dehydroretronecine) derivatized cysteine
-def: "modification from Unimod Chemical derivative" [PubMed:12175151, Unimod:488]
-synonym: "Dehydropyrrolizidine alkaloid (dehydroretronecine) on cysteines" RELATED Unimod-description []
-synonym: "DHP" RELATED Unimod-interim []
-property_value: DiffAvg "118.16" xsd:float
-property_value: DiffFormula "C 8 H 8 N 1" xsd:string
-property_value: DiffMono "118.065674" xsd:float
-property_value: Formula "C 11 H 13 N 2 S 1" xsd:string
-property_value: MassAvg "205.30" xsd:float
-property_value: MassMono "205.079944" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:488
-is_a: MOD:00848
-is_a: MOD:00905
-
-[Term]
-id: MOD:00942
-name: (4,4,5,5-(2)H4)-L-lysine
-def: "A protein modification that effectively substitutes four (1)H protium atoms with four (2)H deuterium atoms to produce (4,4,5,5-(2)H4)-L-lysine." [OMSSA:180, Unimod:481]
-comment: For SILAC experiments.
-synonym: "4,4,5,5-D4 Lysine" RELATED Unimod-description []
-synonym: "4,4,5,5-tetradeuterolysine" EXACT PSI-MOD-alternate []
-synonym: "Label:2H(4)" RELATED Unimod-interim []
-synonym: "lys-2H4" EXACT OMSSA-label []
-property_value: DiffAvg "4.03" xsd:float
-property_value: DiffFormula "(1)H -4 (2)H 4" xsd:string
-property_value: DiffMono "4.025107" xsd:float
-property_value: Formula "C 6 (1)H 8 (2)H 4 N 2 O 1" xsd:string
-property_value: MassAvg "132.12" xsd:float
-property_value: MassMono "132.120070" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:481
-is_a: MOD:00837
-is_a: MOD:00912
-
-[Term]
-id: MOD:00943
-name: 4-trimethylammoniumbutanoyl derivatized residue
-def: "modification from Unimod Isotopic label" [PubMed:12643539, Unimod:476]
-synonym: "4-trimethyllammoniumbutyryl-" RELATED Unimod-description []
-synonym: "TMAB" RELATED Unimod-interim []
-property_value: DiffAvg "128.19" xsd:float
-property_value: DiffFormula "C 7 H 14 N 1 O 1" xsd:string
-property_value: DiffMono "128.107539" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:476
-is_a: MOD:00848
-
-[Term]
-id: MOD:00944
-name: d9-4-trimethylammoniumbutanoyl derivatized residue
-def: "modification from Unimod Isotopic label" [Unimod:477]
-synonym: "d9-4-trimethyllammoniumbutyryl-" RELATED Unimod-description []
-synonym: "TMAB:2H(9)" RELATED Unimod-interim []
-property_value: DiffAvg "137.16" xsd:float
-property_value: DiffFormula "C 7 (1)H 5 (2)H 9 N 1 O 1" xsd:string
-property_value: DiffMono "137.164030" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:477
-relationship: derives_from MOD:00943
-is_a: MOD:01431
-
-[Term]
-id: MOD:00945
-name: fluorescein-5-thiosemicarbazide adduct
-def: "OBSOLETE because redundant and identical to MOD:00626. Remap to MOD:00626." [PubMed:18688235]
-property_value: DiffAvg "421.43" xsd:float
-property_value: DiffFormula "C 21 H 15 N 3 O 5 S 1" xsd:string
-property_value: DiffMono "421.073242" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-replaced_by: MOD:00626
-is_obsolete: true
-
-[Term]
-id: MOD:00946
-name: crosslinked residues with loss of ammonia
-def: "A protein modification that crosslinks two residues with a covalent bond and the loss of ammonia." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:00033
-
-[Term]
-id: MOD:00947
-name: DeltaMass
-def: "Entries from DeltaMass see http://www.abrf.org/index.cfm/dm.home?AvgMass=all." [PubMed:18688235]
-is_a: MOD:00032
-
-[Term]
-id: MOD:00948
-name: 5'-dephospho
-def: "OBSOLETE because this is a modification that occurs to DNA/RNA and not proteins. modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: -79
-property_value: Origin "X" xsd:string
-is_obsolete: true
-
-[Term]
-id: MOD:00949
-name: desmosine
-def: "OBSOLETE because redundant and identical to MOD:01933. Remap to MOD:01933." [DeltaMass:0]
-comment: From DeltaMass: Average Mass: -58
-property_value: Origin "K" xsd:string
-replaced_by: MOD:01933
-is_obsolete: true
-
-[Term]
-id: MOD:00950
-name: decomposed carboxymethylated methionine
-def: "OBSOLETE because this modification has not been seen/reported on since this original publication in 1994 and carboxymethylation of proteins is common enough for this mass shift to have been seen in the intervening 25+ years. modification from DeltaMass" [DeltaMass:3]
-comment: From DeltaMass: Average Mass: -48 Average Mass Change:-48 References:Anal. Biochem. Vol 216 No.1 p141
-property_value: Origin "M" xsd:string
-is_obsolete: true
-
-[Term]
-id: MOD:00951
-name: L-gamma-carboxyglutamic acid with neutral loss of carbon dioxide
-def: "Covalent modification of a peptide or protein L-glutamic acid residue to gamma-carboxyglutamic acid with secondary loss of a neutral carbon dioxide molecular fragment." [DeltaMass:58]
-comment: From DeltaMass: Average Mass: -44 Formula:CO2 Average Mass Change:-44 References:Nakamura T, Yu Z, Fainzilber M, Burlingame AL. Protein Sci (1996) 5, 524-530 Mass spectrometric-based revision of the structure of a cysteine-rich peptide toxin with gamma-carboxyglutamic acid, TxVIIA, from the sea snail, Conus textile. Notes: The elimination of CO2 will regenerate glutamate as if there was no modification. However, peaks appearing with an interval of 44 is quite characteristic. It would be noteworthy to remind that loss of 44 from a gamma-carboxyglutamate-containing peptide may be observed not only as a result of spontaneous decarboxylation but also as an artifact under some ionization conditions such as negative ion mode MALDI.
-synonym: "d4CbxGlu" EXACT PSI-MOD-label []
-property_value: DiffAvg "-44.01" xsd:float
-property_value: DiffFormula "C -1 H 0 N 0 O -2" xsd:string
-property_value: DiffMono "-43.989829" xsd:float
-property_value: Formula "C 5 H 7 N 1 O 3" xsd:string
-property_value: MassAvg "129.12" xsd:float
-property_value: MassMono "129.042593" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00906
-is_a: MOD:00957
-is_a: MOD:00960
-
-[Term]
-id: MOD:00952
-name: (2-aminosuccinimidyl)acetic acid (Asp)
-def: "A protein modification that crosslinks an aspartic acid and the following glycine residue with the formation of (2-aminosuccinimidyl)acetic acid and the loss of a water molecule." [PubMed:10801322, RESID:AA0441#ASP]
-comment: Cross-link 2; this cross-link is formed by the condensation of an aspartic acid residue with the alpha-amido of the following residue.
-subset: PSI-MOD-slim
-synonym: "(2-aminosuccinimidyl)acetic acid" EXACT RESID-name []
-synonym: "(3-amino-2,5-dioxo-1-pyrrolidinyl)acetic acid" EXACT RESID-alternate []
-synonym: "[(3S)-3-amino-2,5-dioxopyrrolidin-1-yl]acetic acid" EXACT RESID-systematic []
-synonym: "anhydroaspartyl glycine" EXACT RESID-alternate []
-synonym: "aspartimide glycine" EXACT RESID-alternate []
-synonym: "CROSSLNK (2-aminosuccinimidyl)acetic acid (Asp-Gly)" EXACT UniProt-feature []
-synonym: "N-(2-aminosuccinyl)glycine" EXACT RESID-alternate []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 6 H 6 N 2 O 3" xsd:string
-property_value: MassAvg "154.13" xsd:float
-property_value: MassMono "154.037842" xsd:float
-property_value: Origin "D, G" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: uniprot.ptm:PTM-0312
-is_a: MOD:02043
-is_a: MOD:00954
-is_a: MOD:01628
-
-[Term]
-id: MOD:00953
-name: O-(L-isoglutamyl)-L-serine (Glu-Ser)
-def: "A protein modification that effectively crosslinks an L-glutamic acid residue and an L-serine residue by an ester bond and releasing water to form O-(L-isoglutamyl)-L-serine." [DeltaMass:0, PubMed:19035375, RESID:AA0597#ESX]
-comment: Cross-link 2; From DeltaMass: with no citation.
-synonym: "(2S)-2-amino-5-[(2S)-2-amino-2-carboxyethoxy]-5-oxopentanoic acid" EXACT RESID-systematic []
-synonym: "CROSSLNK isoglutamyl serine ester (Ser-Glu)" EXACT UniProt-feature []
-synonym: "O(beta)-(gamma-glutamyl)serine" EXACT RESID-alternate []
-synonym: "O-(L-isoglutamyl)-L-serine" EXACT RESID-name []
-synonym: "O-gamma-Glutamyl- (Crosslink to Serine)" EXACT DeltaMass-label []
-synonym: "O3-(isoglutamyl)-serine" EXACT RESID-alternate []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 8 H 10 N 2 O 4" xsd:string
-property_value: MassAvg "198.18" xsd:float
-property_value: MassMono "198.064057" xsd:float
-property_value: Origin "E, S" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02045
-is_a: MOD:00954
-is_a: MOD:01977
-
-[Term]
-id: MOD:00954
-name: crosslinked residues with loss of water
-def: "A protein modification that crosslinks two residues with a covalent bond and the loss of water." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:00033
-
-[Term]
-id: MOD:00955
-name: alaninohistidine (serine crosslinked to tele or pros nitrogen of histidine)
-def: "A protein modification that effectively crosslinks an L-serine residue and an L-histidine residue to release water and form tele- or pros-(2-amino-2-carboxyethyl)histidine." [DeltaMass:0]
-comment: Cross-link 2; From DeltaMass with no citation or formula: Average Mass: -18. The DeltaMass description \"Serine crosslinked to theta or pi carbon of Histidine\" is incorrect. The histidine ring nitrogens (not carbons) are designated tele or N-tau (not theta), and pros or N-pi [JSG].
-synonym: "beta-alaninohistidine" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 9 H 10 N 4 O 2" xsd:string
-property_value: MassAvg "206.20" xsd:float
-property_value: MassMono "206.080376" xsd:float
-property_value: Origin "H, S" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02048
-is_a: MOD:02055
-is_a: MOD:00954
-
-[Term]
-id: MOD:00956
-name: misincorporation of norleucine for methionine
-def: "modification from DeltaMass" [DeltaMass:10]
-comment: From DeltaMass: Average Mass: -18 Average Mass Change:-18 Notes: It has the same mass as leucine or isoleucine and can be charged on the methionyl t-RNA. This often happens in minimal media-prepared fermentations that are not supplemented with enough free methionine. It gives a mass change of -18 and can often be confused with dehydration.
-property_value: DiffAvg "-18.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0 S -1" xsd:string
-property_value: DiffMono "-17.956421" xsd:float
-property_value: Formula "C 6 H 11 N 1 O 1" xsd:string
-property_value: MassAvg "113.16" xsd:float
-property_value: MassMono "113.084064" xsd:float
-property_value: Origin "M" xsd:string
-is_a: MOD:01026
-
-[Term]
-id: MOD:00957
-name: modified residue with neutral loss of carbon dioxide
-def: "Covalent modification of, or a change resulting in an alteration of the measured molecular mass of, a peptide or protein amino acid residue with a secondary loss of a neutral carbon dioxide molecular fragment." [PubMed:18688235]
-synonym: "dCO2ModRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "-44.01" xsd:float
-property_value: DiffFormula "C -1 H 0 N 0 O -2" xsd:string
-property_value: DiffMono "-43.989829" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00431
-
-[Term]
-id: MOD:00958
-name: crosslink between Arg and His sidechains
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: Cross-link 2; From DeltaMass: Average Mass: -5
-property_value: Origin "H, R" xsd:string
-is_a: MOD:00692
-
-[Term]
-id: MOD:00959
-name: 3,3',5,5'-TerTyr (Crosslink)
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: Cross-link 4; From DeltaMass: Average Mass: -4
-property_value: Origin "Y, Y, Y, Y" xsd:string
-is_a: MOD:00692
-
-[Term]
-id: MOD:00960
-name: decarboxylated residue
-def: "A protein modification that effectively replaces a carboxylic acid group with a hydrogen atom." [PubMed:18688235]
-property_value: DiffAvg "-44.01" xsd:float
-property_value: DiffFormula "C -1 H 0 N 0 O -2" xsd:string
-property_value: DiffMono "-43.989829" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01156
-
-[Term]
-id: MOD:00961
-name: reduction of disulfide crosslink in cystine to two cysteines
-def: "A protein modification that effectively reduces the disulfide bond of cystine to form two cysteine residues." [DeltaMass:333]
-comment: Cross-link 2; this modification destroys the cross-link. From DeltaMass: Treatment of cystine (cys-cys) by reducing agents such as dithiothreitol (DTT) or triscarboxyethylphosphine (TCEP) results in cleavage of the disulphide bond and reduction of the sulphur atom of each molecule to create cysteine.
-subset: PSI-MOD-slim
-property_value: DiffAvg "2.02" xsd:float
-property_value: DiffFormula "C 0 H 2 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "2.015650" xsd:float
-property_value: Formula "C 6 H 10 N 2 O 2 S 2" xsd:string
-property_value: MassAvg "206.28" xsd:float
-property_value: MassMono "206.018370" xsd:float
-property_value: Origin "MOD:00034" xsd:string
-is_a: MOD:00905
-is_a: MOD:01473
-relationship: derives_from MOD:00034
-
-[Term]
-id: MOD:00962
-name: 2',3'-dihydrotryptophan
-def: "A protein modification that by reducing the indole ring system of tryptophan to indoline effectively converts an L-tryptophan residue to 2',3'-dihydrotryptophan." [DeltaMass:343, URL:http\://dx.doi.org/10.1016/S0040-4039(00)99113-5]
-comment: From DeltaMass: References:1. Pearson,D.A., Blanchette,M., Baker,M.L. and Guindon,C.A. (1989) Trialkylsilanes as scavengers for the trifluoroacetic acid deblocking ofprotecting groups in peptide synthesis. Tetrahedron Lett., 30(21), 2739-2742 Notes: Reduction of indole double bond of Trp which occurs when triethylsilane (TES) is used as a scavenger and Trp is incorporated without protection of indole nitrogen [1]. This side reaction is likely to be accompanied by oxidation of indoline ring with formation of intensively colored peptide by-products. Triisopropylsilane (TIPS) does not give this side reaction. See structure at http://www.abrf.org/images/misc/dmass2.gif. [However, the pictured indoline structure is incorrect - JSG].
-property_value: DiffAvg "2.02" xsd:float
-property_value: DiffFormula "C 0 H 2 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "2.015650" xsd:float
-property_value: Formula "C 11 H 12 N 2 O 1" xsd:string
-property_value: MassAvg "188.23" xsd:float
-property_value: MassMono "188.094963" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00918
-is_a: MOD:01473
-
-[Term]
-id: MOD:00963
-name: Oxidation of Trp to kynurenine
-def: "Modification from DeltaMass. OBSOLETE because redundant and identical to MOD:00462. Remap to MOD:00462." [DeltaMass:357]
-comment: From DeltaMass: Average Mass: 4 Monoisotopic Mass Change:3.995 Average Mass Change:3.989 References:Ruoppolo M, Amoresano A, Pucci P, Pascarella S, Polticelli F, Trovato M,Menegatti E, Ascenzi P.Characterization of five new low-molecular-mass trypsin inhibitors fromwhite mustard (Sinapis alba L.) seed.Eur J Biochem. 2000 267:6486-92. Notes: See structure at http://www.abrf.org/images/misc/dmass32.jpg.
-property_value: Origin "W" xsd:string
-property_value: Source "artifact" xsd:string
-replaced_by: MOD:00462
-is_obsolete: true
-
-[Term]
-id: MOD:00964
-name: lysine epsilon amino to imine + 12 amu
-def: "modification from DeltaMass" [DeltaMass:34]
-comment: From DeltaMass: Average Mass: 12 Average Mass Change: 12 References: Mathews, W. Rodney; Runge, Thomas A.; Haroldsen, Peter E.; Gaskell, Simon J. (1989) Characterization of impurities in a synthetic renin substrate peptide by fast-atom bombardment mass spectrometry and hybrid tandem mass spectrometry. Rapid Commun. Mass Spectrom. 3(9), 314-19 Notes: Fast-atom bombardment mass spectrometry of a synthetic renin substrate decapeptide (Pro-His-Pro-Phe-His-Leu-Val-Ile-His-D-Lys) indicated the presence of several side products, including a component 12 Da higher in mass. Low-energy collisionally activated ***decompn*** analyses were performed using a hybrid tandem instrument and demonstrated that the heavier side product had two components, in which the structural modification was either at the N- or the C-terminus. Addnl. analyses of the N-acetyl deriv. indicated that for each component the structural modification blocked a site of N-acetylation. It is suggested that the formation of these side products is attributable to the generation of formaldehyde, during removal of the histidine protecting group (benzyloxymethyl), which reacts with the N-terminus of the peptide to give an imidazolidinone structure or with the D- ***lysine***.epsilon.-amine group to yield an ***imine*** . While the precise genesis of the side-products remains speculative, it is clear that the combined strategy of derivatization and tandem mass spectrometry has allowed structural conclusions concerning individual components of an isobaric mixt.
-synonym: "N6-(methylidene)-lysine" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "12.01" xsd:float
-property_value: DiffFormula "C 1 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "12.000000" xsd:float
-property_value: Formula "C 7 H 12 N 2 O 1" xsd:string
-property_value: MassAvg "140.19" xsd:float
-property_value: MassMono "140.094963" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:00965
-name: 4-thiazolidinecarboxylic acid
-def: "A protein modification that effectively converts an N-terminal L-cysteine residue by a formadehyde adduct to 4-thiazolidinecarboxylic acid." [DeltaMass:342]
-comment: From DeltaMass: References: Mitchell, M.A., Runge, T.A., Mathews, W.R., Ichhpurani, A.K., Harn, N.K., Dobrowolski, P.J. and Eckenrrrode, F.M. Problems associated with use of the benzylozymethyl protecting group for histidines. Formaldehyde adducts formed during cleavage by hydrogen fluoride. Int. J. Pept. Protein Res. 1990, 36(4), 350-355. Gesquiere, J.-C., Diesis, E. and Tartar, A. Conversion of N-terminal cysteine to thiazolidine carboxylic acid during hydrogen fluoride deprotection of peptides containing pi-N-Bom protected histidine. J. Chem. Soc. Chem. Commun. 1990, (20), 1402-1403. Kumagaye, K.Y., Inui, T., Nakajima, K., Kimura,T. and Sakakibara, S. Suppression of a side reaction associated with Nim-benzyloxymethyl group during synthesis of peptides containing cysteinyl residue at the N-terminus. Pept. Res. 1991, 4(2), 84-87. Colombo, R., Colombo, F. and Jones, J.H. Acid-labile histidine side-chain protection. The N(pi)-t-butoxymethyl group. J. Chem. Soc. Chem. Commun. 1984, (5), 292-293. Notes: Conversion of N-term Cys to thiazolidine during HF deprotection of His(Bom)-containing peptides [1-3]. See structure at http://www.abrf.org/images/misc/dmass12b.gif; modification in red. This modification cannot be excluded during final deprotection/cleavage in Fmoc-chemistry in cases when His(Bum) was employed [4]. For formation of free imino acid see PubMed:1527501.
-synonym: "thioproline" EXACT DeltaMass-label []
-property_value: DiffAvg "12.01" xsd:float
-property_value: DiffFormula "C 1 H 0 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "12.000000" xsd:float
-property_value: Formula "C 4 H 6 N 1 O 1 S 1" xsd:string
-property_value: MassAvg "116.16" xsd:float
-property_value: MassMono "116.017010" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00905
-
-[Term]
-id: MOD:00966
-name: 1,2,3,4-tetrahydro-beta-carboline-3-carboxylic acid
-def: "A protein modification that effectively converts an N-terminal L-tryptophan residue by a formadehyde adduct to 1,2,3,4-tetrahydro-beta-carboline-3-carboxylic acid." [DeltaMass:339]
-comment: From DeltaMass: Average Mass: 12 Average Mass Change: 12 References: Lippke, K. P., W. G. Schunack, W. Wenning, W. E. Mueller. 1983..beta.-Carbolines as benzodiazepine receptor ligands. 1. Synthesis andbenzodiazepine receptor interaction of esters of.beta.-carboline-3-carboxylic acid. J. Med. Chem.26: 499-503 Cain, M., R. W. Weber, F. Guzman, J. M. Cook, S. A. Barker, K. C.Rice, J. N. Crawley, S. M. Paul, P. Skolnick. 1982. .beta.-Carbolines:synthesis and neurochemical and pharmacological actions on brainbenzodiazepine receptors.J. Med. Chem. 25: 1081-91 Notes: +12 Da modification corresponds to formaldehyde adduct of Trp having beta-carboline structure (methylene bridge links carbon-2 of indole ring and alfa-N. See structure at http://www.abrf.org/images/misc/dmass12a.gif; modification in red.
-property_value: DiffAvg "12.01" xsd:float
-property_value: DiffFormula "C 1 H 0 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "12.000000" xsd:float
-property_value: Formula "C 12 H 10 N 2 O 1" xsd:string
-property_value: MassAvg "198.22" xsd:float
-property_value: MassMono "198.079313" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00918
-
-[Term]
-id: MOD:00967
-name: syndesine
-def: "A protein modification that effectively cross-links two L-lysine residues to form syndesine, hydroxylysinohydroxynorleucine." [DeltaMass:35, PubMed:75151974]
-comment: Cross-link 2; From DeltaMass: Average Mass: 13 Average Mass Change: 13 (incorrect) [JSG].
-synonym: "hydroxylysinohydroxynorleucine" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "16.96" xsd:float
-property_value: DiffFormula "C 0 H -3 N -2 O 3" xsd:string
-property_value: DiffMono "16.955121" xsd:float
-property_value: Formula "C 12 H 21 N 2 O 5" xsd:string
-property_value: MassAvg "273.31" xsd:float
-property_value: MassMono "273.145047" xsd:float
-property_value: Origin "K, K" xsd:string
-is_a: MOD:02051
-
-[Term]
-id: MOD:00968
-name: CM-Cys vs PAM-Cys
-def: "OBSOLETE because this isn't a protein modification, but rather the difference between two known modifications. modification from DeltaMass" [DeltaMass:347]
-comment: From DeltaMass: Average Mass: 13 Formula:C2H2O2 vs C3H5ON Monoisotopic Mass Change:13.03 Average Mass Change:13.05 Notes:Residual acrylamide in SDS gels can partly label cysteine residues in proteins (propionamido-Cys, PAM-Cys, DeltaMass +71Da; see entry). Subsequent alkylation of protein bands with iodoacetic acid e.g. in preparation for proteomic analysis, will convert remaining free cysteines into carboxymethyl-Cys (CM-Cys, DeltaMass +58Da; see entry). Peptide mass fingerprinting may therefore potentially reveal the same cysteine-containing peptide in two forms, differing in mass by 13Da. The relative ratios of the peaks will depend on the initial degree of labelling with acrylamide. Use of high quality, deionised acrylamide in the SDS gel will minimise modification of cysteine through this route. Where it remains a problem, deliberate alkylation using acrylamide instead of iodoacetamide will ensure chemical homogeneity of the final product.
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-is_obsolete: true
-
-[Term]
-id: MOD:00969
-name: CAM-Cys vs PAM-Cys
-def: "OBSOLETE because this isn't a protein modification, but rather the difference between two known modifications. modification from DeltaMass" [DeltaMass:346]
-comment: From DeltaMass: Average Mass: 14 Formula:CH2 Monoisotopic Mass Change:14.016 Average Mass Change:14.027 Notes: Residual acrylamide in SDS gels can partly label cysteine residues in proteins (propionamido-Cys, PAM-Cys, DeltaMass +71Da; see entry). Subsequent alkylation of protein bands with iodoacetamide e.g. in preparation for proteomic analysis, will convert remaining free cysteines into carboxamidomethyl-Cys (CAM-Cys, DeltaMass +57Da; see entry). Peptide mass fingerprinting may therefore potentially reveal the same cysteine-containing peptide in two forms, differing in mass by 14Da. The relative ratios of the peaks will depend on the initial degree of labelling with acrylamide. Use of high quality, deionised acrylamide in the SDS gel will minimise modification of cysteine through this route. Where it remains a problem, deliberate alkylation using acrylamide instead of iodoacetamide will ensure chemical homogeneity of the final product.
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-is_obsolete: true
-
-[Term]
-id: MOD:00970
-name: delta-hydroxy-allysine (Lys)
-def: "modification from DeltaMass" [DeltaMass:37]
-comment: From DeltaMass: Average Mass: 15 Average Mass Change:15 Notes:In going from Lys to hydroxy-allysine, two separate reactions are involved:1. the oxidative deamination converting Lys to allysine (-CH2NH2 being converted to -CHO) with a net mass change of -1;2.conversion of allysine to delta-hydroxy-allysine (-CH2-CHO being converted to -CH(OH)-CHO) with a mass change of +16. The net change from Lys to hydroxyallysine thus is +15.
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:00971
-name: 2-Oxohistidine
-def: "A protein modification that effectively converts an L-histidine residue to 2-oxohistidine." [PubMed:8405458, DeltaMass:38]
-comment: From DeltaMass: Average Mass: 16 Average Mass Change:16 References:Lewisch, S. A. and Levine, R. L. (1995) Anal. Biochem. 231, 440-446. Determination of 2-oxo-histidine by amino acid analysis Notes:Rod LevineNIHBldg 3, Room 106 MSC 0320Bethesda, MD 20892-0320email: rlevine@nih.govvoice: 1 (301) 496-2310fax: 1 (301) 496-0599
-property_value: DiffAvg "16" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 6 H 7 N 3 O 2" xsd:string
-property_value: MassAvg "153.14" xsd:float
-property_value: MassMono "153.053826" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00909
-is_a: MOD:00677
-
-[Term]
-id: MOD:00972
-name: monobrominated L-phenylalanine
-def: "A protein modification that effectively converts an L-phenylalanine residue to a monobrominated L-phenylalanine, such as L-2'-bromophenylalanine." [Unimod:340#F]
-comment: From DeltaMass: Average Mass: 78 Average Mass Change:78 References:Yoshino,K et.al. Biochemistry Vol. 30 pg 6203-9 (1991) Identifidation of a novel amino acid, o-bromo-L-phenylananine, in egg-associated peptides that activate spermatozoa
-synonym: "Br1Phe" EXACT PSI-MOD-label []
-synonym: "bromination" RELATED Unimod-description []
-synonym: "Bromo" RELATED PSI-MS-label []
-property_value: DiffAvg "78.90" xsd:float
-property_value: DiffFormula "Br 1 C 0 H -1 N 0 O 0" xsd:string
-property_value: DiffMono "77.910512" xsd:float
-property_value: Formula "Br 1 C 9 H 8 N 1 O 1" xsd:string
-property_value: MassAvg "226.07" xsd:float
-property_value: MassMono "224.978926" xsd:float
-property_value: Origin "F" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:340
-is_a: MOD:02086
-is_a: MOD:01912
-
-[Term]
-id: MOD:00973
-name: Oxidation of proline (to glutamic acid)
-def: "modification from DeltaMass" [DeltaMass:355]
-comment: From DeltaMass: Average Mass: 32 Monoisotopic Mass Change:31.99 Average Mass Change:32 References:Amici A, Levine, RL, Tsai, L, and Stadtman, ER: Conversion of amino acid residues in proteins and amino acid homopolymers to carbonyl derivatives by metal-catalyzed oxidation reactions. Journal of Biological Chemistry 264: 3341-3346 1989.Rod Levine (unpublished)
-property_value: Origin "P" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:00974
-name: (35)Cl labeled 3'-chlorotyrosine
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 34
-property_value: DiffAvg "33.96" xsd:float
-property_value: DiffFormula "(35)Cl 1 H -1" xsd:string
-property_value: DiffMono "33.961028" xsd:float
-property_value: Formula "C 9 (35)Cl 1 H 8 N 1 O 2" xsd:string
-property_value: MassAvg "197.02" xsd:float
-property_value: MassMono "197.024356" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-relationship: derives_from MOD:01046
-is_a: MOD:00987
-
-[Term]
-id: MOD:00975
-name: (37)Cl labeled 3'-chlorotyrosine
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 36
-property_value: DiffAvg "35.96" xsd:float
-property_value: DiffFormula "(37)Cl 1 H -1" xsd:string
-property_value: DiffMono "35.958078" xsd:float
-property_value: Formula "C 9 (37)Cl 1 H 8 N 1 O 2" xsd:string
-property_value: MassAvg "199.02" xsd:float
-property_value: MassMono "199.021406" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-relationship: derives_from MOD:01046
-is_a: MOD:00987
-
-[Term]
-id: MOD:00976
-name: potassium salt
-def: "modification from DeltaMass - OBSOLETE because redundant and identical to MOD:01072. Remap to MOD:01072." [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 38
-property_value: DiffAvg "38.09" xsd:float
-property_value: DiffFormula "H -1 K 1" xsd:string
-property_value: DiffMono "37.955882" xsd:float
-property_value: Origin "X" xsd:string
-replaced_by: MOD:01072
-is_obsolete: true
-
-[Term]
-id: MOD:00977
-name: disodium salt
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 44
-subset: PSI-MOD-slim
-property_value: DiffAvg "43.96" xsd:float
-property_value: DiffFormula "H -2 Na 2" xsd:string
-property_value: DiffMono "43.963888" xsd:float
-property_value: Origin "X" xsd:string
-is_a: MOD:00747
-
-[Term]
-id: MOD:00978
-name: piperidine adduct to C-terminal Cys
-def: "modification from DeltaMass" [DeltaMass:345]
-comment: From DeltaMass: Average Mass: 51 Average Mass Change: 51 References:Lukszo, Patterson, Albericio, and Kates, Letters in Peptide Science 3, 157-166(1996) Notes:The side reaction can be very significant, and the level to which it occurs depends on how the C-terminal Cys is anchored and what the side-chain protecting group is. The mechanism involves piperidine-mediated beta-elimination of sulfur (with the protecting group on), followed by addition of piperidine across the C-terminaldehydroalanine. Since this last-mentioned step creates a chiral center, a mixture of diastereomers is formed which in special cases can be separatedby HPLC. Another problem with C-terminal Cys is racemization; some references in the review article by Andreu, Albericio, Sole, Munson, Ferrer, and Barany in Pennington-Dunn Peptide Synthesis and Purification Protocols, vol 35, 1994, pp. 91-169.
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:00979
-name: t-butyl ester (OtBu) and t-butyl (tBu)
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 56
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:00980
-name: Carboxamidomethyl (on Cysteine)
-def: "modification from DeltaMass - OBSOLETE because redundant, the difference component of MOD:01060. Remap to MOD:01060." [DeltaMass:337]
-comment: From DeltaMass: Average Mass: 57 Abbreviation:CamCys Formula:C2H3NO Monoisotopic Mass Change:57.021 Average Mass Change:57.051 Notes:Cysteine reacts with iodoacetamide to produce carboxamidomethyl cysteine. Alternative names are often used, such as amidocarboxymethylcysteine and carbamoylmethylcysteine
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-replaced_by: MOD:01060
-is_obsolete: true
-
-[Term]
-id: MOD:00981
-name: sodium and potassium salt
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 60
-subset: PSI-MOD-slim
-property_value: DiffAvg "60.07" xsd:float
-property_value: DiffFormula "H -2 K 1 Na 1" xsd:string
-property_value: DiffMono "59.937826" xsd:float
-property_value: Origin "X" xsd:string
-is_a: MOD:00747
-is_a: MOD:00849
-
-[Term]
-id: MOD:00982
-name: L-selenocysteine (Ser)
-def: "A protein modification that effectively converts an L-serine residue to L-selenocysteine (not known as a natural post-translational modification process)." [DeltaMass:0]
-comment: [From DeltaMass: Average Mass: 64.] Although selenocysteine-charged tRNA(Sec) is biosynthesized from serine-charged tRNA(Sec), in peptide work selenocysteine is usually considered as either a natural residue or as a modified cysteine residue. This entry is for the artifactual formation of L-selenocysteine from serine. For encoded L-selenocysteine, use MOD:00031 [JSG].
-synonym: "Sec(Ser)" EXACT PSI-MOD-label []
-synonym: "Selenocysteine (from Serine)" EXACT DeltaMass-label []
-property_value: DiffAvg "62.97" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O -1 Se 1" xsd:string
-property_value: DiffMono "63.921607" xsd:float
-property_value: Formula "C 3 H 5 N 1 O 1 Se 1" xsd:string
-property_value: MassAvg "150.05" xsd:float
-property_value: MassMono "150.953635" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00916
-is_a: MOD:02088
-
-[Term]
-id: MOD:00983
-name: Asp transamidation with piperidine
-def: "modification from DeltaMass" [DeltaMass:67]
-comment: From DeltaMass: Average Mass: 67 Average Mass Change:67 References:http://www.abrf.org/archives/hmail/0008/0007.html Notes:1.) Get rid of the DBU. It can cause piperidine amides at Asp residues. The tbu ester side chain comes off during synthesis and the residue is trans-amidated with piperidine (+67Da by MS). If you haven't yet seen this, you will. Even \"normal\" 20% pip/DMF (NMP) will cause this, but less frequently. Literature exists for this; I don't remember the exact reference. David H. Singleton Scientist Pfizer Central Research PO Box 8118-101 Eastern Point Road Groton, CT 06340 (860)441-4404.
-property_value: Origin "D" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:00984
-name: (35)Cl labeled 3',5'-dichlorotyrosine
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 68
-property_value: DiffAvg "67.92" xsd:float
-property_value: DiffFormula "(35)Cl 2 H -2" xsd:string
-property_value: DiffMono "67.922055" xsd:float
-property_value: Formula "C 9 (35)Cl 2 H 7 N 1 O 2" xsd:string
-property_value: MassAvg "230.99" xsd:float
-property_value: MassMono "230.985384" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-relationship: derives_from MOD:01045
-is_a: MOD:00987
-
-[Term]
-id: MOD:00985
-name: halogenated tyrosine
-def: "A protein modification that effectively substitutes a hydrogen atom of an L-tyrosine residue with a halogen atom." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "HalTyr" EXACT PSI-MOD-label []
-property_value: Origin "Y" xsd:string
-is_a: MOD:00694
-is_a: MOD:00919
-
-[Term]
-id: MOD:00986
-name: (35)Cl and (37)Cl labeled 3',5'-dichlorotyrosine
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 70.
-property_value: DiffAvg "69.92" xsd:float
-property_value: DiffFormula "(35)Cl 1 (37)Cl 1 H -2" xsd:string
-property_value: DiffMono "69.919105" xsd:float
-property_value: Formula "C 9 (35)Cl 1 (37)Cl 1 H 7 N 1 O 2" xsd:string
-property_value: MassAvg "232.98" xsd:float
-property_value: MassMono "232.982434" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-relationship: derives_from MOD:01045
-is_a: MOD:00987
-
-[Term]
-id: MOD:00987
-name: chlorinated tyrosine
-def: "A protein modification that effectively substitutes a hydrogen atom of an L-tyrosine residue with a chlorine atom." [PubMed:18688235]
-synonym: "ClTyr" EXACT PSI-MOD-label []
-property_value: Origin "Y" xsd:string
-is_a: MOD:00753
-is_a: MOD:00985
-
-[Term]
-id: MOD:00988
-name: brominated tyrosine
-def: "A protein modification that effectively substitutes a hydrogen atom of an L-tyrosine residue with a bromine atom." [PubMed:18688235]
-synonym: "BrTyr" EXACT PSI-MOD-label []
-property_value: Origin "Y" xsd:string
-is_a: MOD:00754
-is_a: MOD:00985
-
-[Term]
-id: MOD:00989
-name: acetamidomethyl (Acm)
-def: "OBSOLETE because redundant, the difference component of MOD:01079. Remap to MOD:01079." [DeltaMass:0]
-comment: From DeltaMass with no citation or formula.
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-replaced_by: MOD:01079
-is_obsolete: true
-
-[Term]
-id: MOD:00990
-name: (37)Cl labeled 3',5'-dichlorotyrosine
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 72
-property_value: DiffAvg "71.92" xsd:float
-property_value: DiffFormula "(37)Cl 2 H -2" xsd:string
-property_value: DiffMono "71.916155" xsd:float
-property_value: Formula "C 9 (37)Cl 2 H 7 N 1 O 2" xsd:string
-property_value: MassAvg "234.98" xsd:float
-property_value: MassMono "234.979484" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-relationship: derives_from MOD:01045
-is_a: MOD:00987
-
-[Term]
-id: MOD:00991
-name: S-(sn-1-glyceryl)-L-cysteine
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 74 with no citation.
-property_value: DiffAvg "74.08" xsd:float
-property_value: DiffFormula "C 3 H 6 O 2" xsd:string
-property_value: DiffMono "74.036779" xsd:float
-property_value: Formula "C 6 H 11 N 1 O 3 S 1" xsd:string
-property_value: MassAvg "177.22" xsd:float
-property_value: MassMono "177.045964" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:00992
-name: glutamate 5-glycerol ester
-def: "modification from DeltaMass" [DeltaMass:78, PubMed:18767873]
-comment: From DeltaMass: Average Mass: 74 Average Mass Change: 74 References: Anal. Biochem. 1993 Vol 208 No. 2 382-386, PubMed:8452236. [DeltaMass] This article only suggests this as a possible modification and does no characterization. Isolation and stuctural evidence for artifactual modification are found in PubMed:18767873 [JSG].
-property_value: DiffAvg "74.08" xsd:float
-property_value: DiffFormula "C 3 H 6 O 2" xsd:string
-property_value: DiffMono "74.036779" xsd:float
-property_value: Formula "C 8 H 13 N 1 O 5" xsd:string
-property_value: MassAvg "203.19" xsd:float
-property_value: MassMono "203.079373" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00906
-
-[Term]
-id: MOD:00993
-name: phenyl ester
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 76, on acidic amino acids
-synonym: "OPh" EXACT DeltaMass-label []
-property_value: DiffAvg "76.10" xsd:float
-property_value: DiffFormula "C 6 H 4" xsd:string
-property_value: DiffMono "76.031300" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-
-[Term]
-id: MOD:00994
-name: (79)Br labeled 3'-bromotyrosine
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 78
-property_value: DiffAvg "77.91" xsd:float
-property_value: DiffFormula "(79)Br 1 H -1" xsd:string
-property_value: DiffMono "77.910512" xsd:float
-property_value: Formula "(79)Br 1 C 9 H 8 N 1 O 2" xsd:string
-property_value: MassAvg "240.97" xsd:float
-property_value: MassMono "240.973841" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-relationship: derives_from MOD:01025
-is_a: MOD:01000
-
-[Term]
-id: MOD:00995
-name: (81)Br labeled 2'-bromophenylalanine
-def: "A protein modification that effectively converts an L-phenylalanine residue to (81)Br-L-2'-bromophenylalanine." [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 80
-property_value: DiffAvg "79.91" xsd:float
-property_value: DiffFormula "(81)Br 1 H -1" xsd:string
-property_value: DiffMono "79.908466" xsd:float
-property_value: Formula "(81)Br 1 C 9 H 8 N 1 O 1" xsd:string
-property_value: MassAvg "226.98" xsd:float
-property_value: MassMono "226.976879" xsd:float
-property_value: Origin "F" xsd:string
-property_value: Source "artifact" xsd:string
-relationship: derives_from MOD:00183
-is_a: MOD:02086
-
-[Term]
-id: MOD:00996
-name: (81)Br labeled 3'-bromotyrosine
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 80
-property_value: DiffAvg "79.91" xsd:float
-property_value: DiffFormula "(81)Br 1 H -1" xsd:string
-property_value: DiffMono "79.908466" xsd:float
-property_value: Formula "(81)Br 1 C 9 H 8 N 1 O 2" xsd:string
-property_value: MassAvg "242.97" xsd:float
-property_value: MassMono "242.971794" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-relationship: derives_from MOD:01025
-is_a: MOD:01000
-
-[Term]
-id: MOD:00997
-name: cyclohexyl ester
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 82
-synonym: "OcHex" EXACT DeltaMass-label []
-property_value: DiffAvg "82.15" xsd:float
-property_value: DiffFormula "C 6 H 10" xsd:string
-property_value: DiffMono "82.078250" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-
-[Term]
-id: MOD:00998
-name: iodinated tyrosine
-def: "A protein modification that effectively substitutes a hydrogen atom of an L-tyrosine residue with an iodine atom." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "ITyr" EXACT PSI-MOD-label []
-property_value: Origin "Y" xsd:string
-is_a: MOD:00755
-is_a: MOD:00985
-
-[Term]
-id: MOD:00999
-name: homoseryl lactone
-def: "OBSOLETE because redundant and identical to MOD:00404. Remap to MOD:00404." [DeltaMass:90]
-comment: From DeltaMass: Average Mass: 83 Formula:C4H5O1N1 Monoisotopic Mass Change:83.037 Average Mass Change:83.09
-property_value: Origin "M" xsd:string
-property_value: Source "artifact" xsd:string
-replaced_by: MOD:00404
-is_obsolete: true
-
-[Term]
-id: MOD:01000
-name: monobrominated tyrosine
-def: "A protein modification that effectively substitutes one hydrogen atom of an L-tyrosine residue with one bromine atom." [PubMed:18688235]
-synonym: "Br1Tyr" EXACT PSI-MOD-label []
-property_value: Origin "Y" xsd:string
-is_a: MOD:00988
-
-[Term]
-id: MOD:01001
-name: 2-aminoisobutyric acid residue (Aib)
-def: "A protein modification that inserts or replaces a residue with a 2-aminoisobutyric acid." [DeltaMass:0]
-comment: Modification from DeltaMass: Average Mass: 85.
-synonym: "2-amino-2-methylpropanoic acid" EXACT PSI-MOD-alternate []
-synonym: "2-amino-2-methylpropionic acid" EXACT PSI-MOD-alternate []
-synonym: "2-methylalanine" EXACT PSI-MOD-alternate []
-synonym: "Aib" EXACT PSI-MOD-alternate []
-synonym: "alpha,alpha-dimethylglycine" EXACT PSI-MOD-alternate []
-synonym: "alpha-aminoisobutyric acid" EXACT PSI-MOD-alternate []
-synonym: "alpha-methylalanine" EXACT PSI-MOD-alternate []
-property_value: Formula "C 4 H 7 N 1 O 1" xsd:string
-property_value: MassAvg "85.11" xsd:float
-property_value: MassMono "85.052764" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00850
-
-[Term]
-id: MOD:01002
-name: gamma-aminobutyryl
-def: "modification from DeltaMass" [DeltaMass:92]
-comment: From DeltaMass: Average Mass: 85 Formula: C 4 H 7 O 1 N 1 Monoisotopic Mass Change: 85.053 Average Mass Change: 85.106
-property_value: DiffAvg "85.11" xsd:float
-property_value: DiffFormula "C 4 H 7 N 1 O 1" xsd:string
-property_value: DiffMono "85.052764" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:01003
-name: t-butyloxymethyl (Bum)
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 86
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:01004
-name: diaminopropionyl
-def: "modification from DeltaMass" [DeltaMass:95]
-comment: From DeltaMass: Average Mass: 86 Formula: C 3 H 6 O 2 N 1 Monoisotopic Mass Change: 86.048 Average Mass Change: 86.094
-property_value: DiffAvg "86.09" xsd:float
-property_value: DiffFormula "C 3 H 6 N 2 O 1" xsd:string
-property_value: DiffMono "86.048013" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:01005
-name: t-butylsulfenyl
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 88
-synonym: "StBu" EXACT DeltaMass-label []
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:01006
-name: dibrominated tyrosine
-def: "A protein modification that effectively substitutes two hydrogen atoms of an L-tyrosine residue with two bromine atoms." [Unimod:534]
-synonym: "Br2Tyr" EXACT PSI-MOD-label []
-synonym: "Dibromo" RELATED PSI-MS-label []
-synonym: "Dibromo" RELATED Unimod-description []
-property_value: Origin "Y" xsd:string
-xref: Unimod:534
-is_a: MOD:00988
-
-[Term]
-id: MOD:01007
-name: anisyl modified residue
-def: "A protein modification that effectively substitutes an anisyl (methoxyphenyl) group for a hydroxyl group, typically at the 4 or para position." [DeltaMass:0]
-comment: From DeltaMass with no citation or formula: Average Mass: 90.
-property_value: DiffAvg "90.13" xsd:float
-property_value: DiffFormula "C 7 H 6" xsd:string
-property_value: DiffMono "90.046950" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-
-[Term]
-id: MOD:01008
-name: benzyl (Bzl) and benzyl ester (OBzl) modified residue
-def: "A protein modification that effectively substitutes a benzyl (phenylmethyl) group for a hydrogen atom." [DeltaMass:0]
-comment: From DeltaMass with no citation or formula: Average Mass: 90
-property_value: DiffAvg "90.13" xsd:float
-property_value: DiffFormula "C 7 H 6" xsd:string
-property_value: DiffMono "90.046950" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-
-[Term]
-id: MOD:01009
-name: dehydrogenated proline
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass with no citation.
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 5 H 5 N 1 O 1" xsd:string
-property_value: MassAvg "95.10" xsd:float
-property_value: MassMono "95.037114" xsd:float
-property_value: Origin "P" xsd:string
-is_a: MOD:00915
-is_a: MOD:01888
-
-[Term]
-id: MOD:01010
-name: trifluoroacetylated residue
-def: "A protein modification that effectively substitutes a trifluoroacetyl group for a hydrogen atom." [DeltaMass:0]
-synonym: "TFA" EXACT DeltaMass-label []
-property_value: DiffAvg "96.01" xsd:float
-property_value: DiffFormula "C 2 F 3 H -1 O 1" xsd:string
-property_value: DiffMono "95.982299" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00498
-is_a: MOD:00649
-is_a: MOD:00848
-
-[Term]
-id: MOD:01011
-name: N-hydroxysuccinimide (ONSu, OSu)
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 97
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:01012
-name: oxidation of disulfide crosslink in cystine to two cysteic acids
-def: "A protein modification that effectively oxidizes the disulfide bond of a cystine crosslink to form two cysteic acid residues." [DeltaMass:335]
-comment: Cross-link 2. This modification destroys a cross-link. From DeltaMass: Average Mass: 98 Abbreviation: Cya Average Mass Change: 98 Notes: Treatment of cystine by strongly oxidising reagents such as performic acid results in the breakage of the disulphide bond and complete oxidation of the sulphur atoms on each molecule. Such treatment is often carried out prior to amino acid analysis as the resulting cysteic acid is then resistant to acid degradation during the hydrolysis procedure.
-property_value: DiffAvg "98.01" xsd:float
-property_value: DiffFormula "C 0 H 2 N 0 O 6 S 0" xsd:string
-property_value: DiffMono "97.985138" xsd:float
-property_value: Formula "C 6 H 10 N 2 O 8 S 2" xsd:string
-property_value: MassAvg "302.27" xsd:float
-property_value: MassMono "301.987857" xsd:float
-property_value: Origin "MOD:00034" xsd:string
-property_value: Source "artifact" xsd:string
-relationship: derives_from MOD:00034
-is_a: MOD:00675
-
-[Term]
-id: MOD:01013
-name: tetramethylguanidinium termination by-product on amine
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 98
-property_value: Origin "X" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:01014
-name: phosphate/sulphate adduct of proteins
-def: "modification from DeltaMass" [DeltaMass:358]
-comment: From DeltaMass: Average Mass: 98 Formula:H3PO4 or H2SO4 Monoisotopic Mass Change:97.97 Average Mass Change:98 Notes:Proteins may pick up non-covalent salt adducts during purification. Phosphate and sulphate salts are commonly used and may be observed as +98 amu adducts (or multiples thereof) forming ion pairs with basic residues. Monoisotopic masses H2SO4 97.967, H3PO4 97.977
-property_value: Origin "X" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:01015
-name: isovaline residue (Iva)
-def: "A protein modification that inserts or replaces a residue with an isovaline." [DeltaMass:110]
-synonym: "2-amino-2-methylbutanoic acid" EXACT PSI-MOD-alternate []
-synonym: "Isovalyl (-I-,-Iva-)" EXACT DeltaMass-label []
-synonym: "Iva" EXACT PSI-MOD-label []
-property_value: Formula "C 5 H 9 N 1 O 1" xsd:string
-property_value: MassAvg "99.13" xsd:float
-property_value: MassMono "99.068414" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00850
-
-[Term]
-id: MOD:01016
-name: t-butyloxycarbonyl
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 100
-synonym: "tBoc" EXACT DeltaMass-label []
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:01017
-name: homoseryl (-Hse-)
-def: "OBSOLETE because redundant and identical to MOD:00403. Remap to MOD:00403." [DeltaMass:113]
-comment: From DeltaMass: Average Mass: 101 Abbreviation:-Hse- Formula:C4H7O2N Monoisotopic Mass Change:101.048 Average Mass Change:101.105
-property_value: Origin "M" xsd:string
-property_value: Source "artifact" xsd:string
-replaced_by: MOD:00403
-is_obsolete: true
-
-[Term]
-id: MOD:01018
-name: 4-methylbenzyl
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 104
-synonym: "Meb" EXACT DeltaMass-label []
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-
-[Term]
-id: MOD:01019
-name: hydroxymethylphenyl linker
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 106
-synonym: "HMP" EXACT DeltaMass-label []
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:01020
-name: thioanisyl
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 106
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:01021
-name: thiocresyl
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 106
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:01022
-name: 2-piperidinecarboxylic acid
-def: "A protein modification that effectively converts an L-lysine residue to 2-piperidinecarboxylic acid." [DeltaMass:0]
-synonym: "Pip" EXACT DeltaMass-label []
-property_value: DiffAvg "-17.03" xsd:float
-property_value: DiffFormula "C 0 H -3 N -1 O 0" xsd:string
-property_value: DiffMono "-17.026549" xsd:float
-property_value: Formula "C 6 H 9 N 1 O 1" xsd:string
-property_value: MassAvg "111.14" xsd:float
-property_value: MassMono "111.068414" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00601
-is_a: MOD:00912
-is_a: MOD:01160
-
-[Term]
-id: MOD:01023
-name: 3',5'-dibromo-L-tyrosine
-def: "A protein modification that effectively converts an L-tyrosine residue to 3',5'-dibromo-L-tyrosine." [DeltaMass:156]
-synonym: "3',5'-Br2Tyr" EXACT PSI-MOD-label []
-property_value: DiffAvg "157.79" xsd:float
-property_value: DiffFormula "Br 2 C 0 H -2 N 0 O 0" xsd:string
-property_value: DiffMono "155.821024" xsd:float
-property_value: Formula "Br 2 C 9 H 7 N 1 O 2" xsd:string
-property_value: MassAvg "320.97" xsd:float
-property_value: MassMono "318.884353" xsd:float
-property_value: Origin "Y" xsd:string
-is_a: MOD:01006
-
-[Term]
-id: MOD:01024
-name: monohydroxylated proline
-def: "A protein modification that effectively converts an L-proline residue to one of several monohydroxylated proline residues, including 3-hydroxy-L-proline and 4-hydroxy-L-proline." [DeltaMass:0, OMSSA:62, Unimod:35#P]
-comment: From DeltaMass: Average Mass: 131. This is the mass of the free amino acid [JSG].
-subset: PSI-MOD-slim
-synonym: "Hy1Pro" EXACT PSI-MOD-label []
-synonym: "hydroxylationp" EXACT OMSSA-label []
-synonym: "Hydroxyproline" EXACT DeltaMass-label []
-synonym: "Hyp" EXACT DeltaMass-label []
-synonym: "Oxidation" RELATED PSI-MS-label []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 5 H 7 N 1 O 2" xsd:string
-property_value: MassAvg "113.12" xsd:float
-property_value: MassMono "113.047678" xsd:float
-property_value: Origin "P" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:35
-xref: uniprot.ptm:PTM-0149
-is_a: MOD:00425
-is_a: MOD:00594
-is_a: MOD:00678
-
-[Term]
-id: MOD:01025
-name: 3'-bromo-L-tyrosine
-def: "A protein modification that effectively converts an L-tyrosine residue to 3'-bromo-L-tyrosine." [PubMed:18688235]
-synonym: "3'-BrTyr" EXACT PSI-MOD-label []
-property_value: DiffAvg "78.90" xsd:float
-property_value: DiffFormula "Br 1 H -1" xsd:string
-property_value: DiffMono "77.910512" xsd:float
-property_value: Formula "Br 1 C 9 H 8 N 1 O 2" xsd:string
-property_value: MassAvg "242.07" xsd:float
-property_value: MassMono "240.973841" xsd:float
-property_value: Origin "Y" xsd:string
-is_a: MOD:01000
-
-[Term]
-id: MOD:01026
-name: norleucine residue (Nle)
-def: "A protein modification that inserts or replaces a residue with a norleucine." [DeltaMass:126]
-synonym: "Nle" EXACT DeltaMass-label []
-property_value: Formula "C 6 H 11 N 1 O 1" xsd:string
-property_value: MassAvg "113.16" xsd:float
-property_value: MassMono "113.084064" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00850
-is_a: MOD:00306
-
-[Term]
-id: MOD:01027
-name: t-amyloxycarbonyl
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 114
-synonym: "Aoc" EXACT DeltaMass-label []
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:01028
-name: monochlorinated L-tyrosine
-def: "A protein modification that effectively substitutes one hydrogen atom of an L-tyrosine residue with one chlorine atom." [PubMed:18688235]
-synonym: "Cl1Tyr" EXACT PSI-MOD-label []
-property_value: DiffAvg "34.44" xsd:float
-property_value: DiffFormula "C 0 Cl 1 H -1 N 0 O 0" xsd:string
-property_value: DiffMono "33.961028" xsd:float
-property_value: Formula "C 9 Cl 1 H 8 N 1 O 2" xsd:string
-property_value: MassAvg "197.62" xsd:float
-property_value: MassMono "197.024356" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00987
-is_a: MOD:01911
-
-[Term]
-id: MOD:01029
-name: succinylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with a succinyl group linked through a carbonyl carbon." [DeltaMass:0, Unimod:64]
-comment: From DeltaMass with no citation or formula, Average Mass: 117 [JSG].
-subset: PSI-MOD-slim
-synonym: "Succinic anhydride labeling reagent light form (N-term & K)" RELATED Unimod-description []
-property_value: DiffAvg "100.07" xsd:float
-property_value: DiffFormula "C 4 H 4 O 3" xsd:string
-property_value: DiffMono "100.016044" xsd:float
-property_value: Origin "X" xsd:string
-xref: Unimod:64
-is_a: MOD:00649
-
-[Term]
-id: MOD:01030
-name: hydroxybenzotriazole ester
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 117
-synonym: "HOBt" EXACT DeltaMass-label []
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:01031
-name: dimethylbenzyl
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 118
-synonym: "diMeBzl" EXACT DeltaMass-label []
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:01032
-name: benzyloxymethyl modified residue
-def: "A protein modification that effectively substitutes a benzyloxymethyl group for a hydrogen atom." [DeltaMass:0]
-synonym: "Bom" EXACT DeltaMass-label []
-property_value: DiffAvg "120.15" xsd:float
-property_value: DiffFormula "C 8 H 8 O 1" xsd:string
-property_value: DiffMono "120.057515" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-
-[Term]
-id: MOD:01033
-name: p-methoxybenzyl modified residue
-def: "A protein modification that effectively substitutes a p-methoxybenzyl group for a hydrogen atom." [DeltaMass:0]
-synonym: "Mbzl" EXACT DeltaMass-label []
-synonym: "Mob" EXACT DeltaMass-label []
-property_value: DiffAvg "120.15" xsd:float
-property_value: DiffFormula "C 8 H 8 O 1" xsd:string
-property_value: DiffMono "120.057515" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-
-[Term]
-id: MOD:01034
-name: 4-nitrophenyl modified residue
-def: "A protein modification that effectively substitutes a 4-nitrophenyl group for a hydrogen atom." [DeltaMass:0]
-synonym: "ONp" EXACT DeltaMass-label []
-synonym: "p-nitrophenyl" EXACT DeltaMass-label []
-property_value: DiffAvg "121.10" xsd:float
-property_value: DiffFormula "C 6 H 3 N 1 O 2" xsd:string
-property_value: DiffMono "121.016378" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-
-[Term]
-id: MOD:01035
-name: chlorobenzyl
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 125
-synonym: "ClBzl" EXACT DeltaMass-label []
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:01036
-name: O-methyl aspartyl
-def: "OBSOLETE because redundant and identical to MOD:01181. Remap to MOD:01181." [PubMed:18688235]
-comment: From DeltaMass:148 (name misspelled \"aspartamyl\", and formula incorrect, N and O reversed) Average Mass: 129 Formula: C5H7O1N3 Monoisotopic Mass Change: 129.042 Average Mass Change: 129.116
-property_value: Formula "C 5 H 7 N 1 O 3" xsd:string
-property_value: MassAvg "129.12" xsd:float
-property_value: MassMono "129.042593" xsd:float
-property_value: Origin "D" xsd:string
-replaced_by: MOD:01181
-is_obsolete: true
-
-[Term]
-id: MOD:01037
-name: dichlorinated tyrosine
-def: "A protein modification that effectively substitutes two hydrogen atoms of an L-tyrosine residue with two chlorine atoms." [PubMed:18688235]
-synonym: "Cl2Tyr" EXACT PSI-MOD-label []
-property_value: DiffAvg "68.88" xsd:float
-property_value: DiffFormula "C 0 Cl 2 H -2 N 0 O 0" xsd:string
-property_value: DiffMono "67.922055" xsd:float
-property_value: Formula "C 9 Cl 2 H 7 N 1 O 2" xsd:string
-property_value: MassAvg "232.06" xsd:float
-property_value: MassMono "230.985384" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00987
-
-[Term]
-id: MOD:01038
-name: norleucine (Nle)
-def: "OBSOLETE because this represents a free amino acid and the corresponding residue is MOD:01026." [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 131.
-is_obsolete: true
-
-[Term]
-id: MOD:01039
-name: hydroxy aspartyl
-def: "OBSOLETE because redundant and identical to MOD:00036. Remap to MOD:00036." [PubMed:18688235]
-comment: From DeltaMass:152 (name misspelled \"aspartamyl\", and formula incorrect, N and O reversed) Average Mass: 131 Formula:C4H5O1N4 Monoisotopic Mass Change:131.022 Average Mass Change:131.088
-property_value: Formula "C 4 H 5 N 1 O 4" xsd:string
-property_value: MassAvg "131.09" xsd:float
-property_value: MassMono "131.021858" xsd:float
-property_value: Origin "D" xsd:string
-replaced_by: MOD:00036
-is_obsolete: true
-
-[Term]
-id: MOD:01040
-name: penicillamine residue
-def: "A protein modification that inserts or replaces a residue with a penicillamine." [DeltaMass:154]
-comment: From DeltaMass: Name misspelled 'bb-dimethyl cystenyl'. No citation provided.
-synonym: "2-amino-3-mercapto-3-methylbutanoic acid" EXACT PSI-MOD-alternate []
-synonym: "2-amino-3-methyl-3-sulfanylbutanoic acid" EXACT PSI-MOD-alternate []
-synonym: "3,3-dimethylcysteine" EXACT PSI-MOD-alternate []
-synonym: "3-mercapto-L-valine" EXACT PSI-MOD-alternate []
-synonym: "beta,beta-dimethylcysteine" EXACT DeltaMass-label []
-synonym: "Pen" EXACT DeltaMass-label []
-synonym: "Pen" EXACT PSI-MOD-alternate []
-property_value: Formula "C 5 H 9 N 1 O 1 S 1" xsd:string
-property_value: MassAvg "131.19" xsd:float
-property_value: MassMono "131.040485" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00850
-
-[Term]
-id: MOD:01041
-name: benzyloxycarbonyl modified residue
-def: "A protein modification that effectively substitutes a benzyloxycarbonyl group for a hydrogen atom." [DeltaMass:0]
-synonym: "Z" EXACT DeltaMass-label []
-property_value: DiffAvg "134.13" xsd:float
-property_value: DiffFormula "C 8 H 6 O 2" xsd:string
-property_value: DiffMono "134.036779" xsd:float
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-
-[Term]
-id: MOD:01042
-name: adamantyl modified residue
-def: "A protein modification that effectively substitutes a adamantyl group for a hydrogen atom." [DeltaMass:0]
-synonym: "Ada" EXACT DeltaMass-label []
-property_value: DiffAvg "134.22" xsd:float
-property_value: DiffFormula "C 10 H 14" xsd:string
-property_value: DiffMono "134.109550" xsd:float
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-
-[Term]
-id: MOD:01043
-name: p-nitrobenzyl ester modified residue
-def: "A protein modification that effectively substitutes a p-nitrobenzyl group for the hydrogen atom of a carboxyl group." [DeltaMass:0]
-synonym: "ONb" EXACT DeltaMass-label []
-property_value: DiffAvg "135.12" xsd:float
-property_value: DiffFormula "C 7 H 5 N 1 O 2" xsd:string
-property_value: DiffMono "135.032028" xsd:float
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-
-[Term]
-id: MOD:01044
-name: N-methyl glutamyl
-def: "OBSOLETE because redundant and identical to MOD:00080. Remap to MOD:00080." [DeltaMass:166]
-comment: From DeltaMass with no citation. Formula:C6H10O2N2 (name misspelled, formula for N5-methylglutaminyl, rather than N2-methylglutamyl)
-property_value: Origin "Q" xsd:string
-replaced_by: MOD:00080
-is_obsolete: true
-
-[Term]
-id: MOD:01045
-name: 3',5'-dichloro-L-tyrosine
-def: "A protein modification that effectively converts an L-tyrosine residue to 3',5'-dichloro-L-tyrosine." [PubMed:18688235]
-synonym: "3',5'-Cl2Tyr" EXACT PSI-MOD-label []
-property_value: DiffAvg "68.88" xsd:float
-property_value: DiffFormula "C 0 Cl 2 H -2 N 0 O 0" xsd:string
-property_value: DiffMono "67.922055" xsd:float
-property_value: Formula "C 9 Cl 2 H 7 N 1 O 2" xsd:string
-property_value: MassAvg "232.06" xsd:float
-property_value: MassMono "230.985384" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01037
-
-[Term]
-id: MOD:01046
-name: 3'-chloro-L-tyrosine
-def: "A protein modification that effectively converts an L-tyrosine residue to 3'-chloro-L-tyrosine." [PubMed:18688235]
-synonym: "3'-ClTyr" EXACT PSI-MOD-label []
-property_value: DiffAvg "34.44" xsd:float
-property_value: DiffFormula "C 0 Cl 1 H -1 N 0 O 0" xsd:string
-property_value: DiffMono "33.961028" xsd:float
-property_value: Formula "C 9 Cl 1 H 8 N 1 O 2" xsd:string
-property_value: MassAvg "197.62" xsd:float
-property_value: MassMono "197.024356" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01028
-
-[Term]
-id: MOD:01047
-name: monohydroxylated lysine
-def: "A protein modification that effectively converts an L-lysine residue to a monohydroxylated lysine." [DeltaMass:168, OMSSA:60, Unimod:35#K]
-comment: From DeltaMass: Average Mass: 144 Abbreviation:-Hyl- Formula:C6H12N2O2 Monoisotopic Mass Change:144.09 Average Mass Change:144.174.
-subset: PSI-MOD-slim
-synonym: "Hy1Lys" EXACT PSI-MOD-label []
-synonym: "Hydroxy Lysyl (-Hyl-)" EXACT DeltaMass-label []
-synonym: "hydroxylationk" EXACT OMSSA-label []
-synonym: "Oxidation" RELATED PSI-MS-label []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 6 H 12 N 2 O 2" xsd:string
-property_value: MassAvg "144.17" xsd:float
-property_value: MassMono "144.089878" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:35
-is_a: MOD:00425
-is_a: MOD:00681
-
-[Term]
-id: MOD:01048
-name: 2-pyrrolidone-5-carboxylic acid
-def: "A protein modification that effectively converts a source amino acid residue to 2-pyrrolidone-5-carboxylic acid." [PubMed:18688235]
-comment: From DeltaMass: Average Mass: -18 Average Mass Change: -18.01 References:The conversion of glutamic acid to pyroglutamic was reported for the beta-amiloid protein. Miller et al. Arch. Biochem. Biophy. (1993) 301, 41-52.
-subset: PSI-MOD-slim
-synonym: "PyrGlu" EXACT PSI-MOD-label []
-property_value: Formula "C 5 H 6 N 1 O 2" xsd:string
-property_value: MassAvg "112.11" xsd:float
-property_value: MassMono "112.039853" xsd:float
-property_value: Origin "X" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00601
-is_a: MOD:00859
-
-[Term]
-id: MOD:01049
-name: halogenated histidine
-def: "A protein modification that effectively substitutes a hydrogen atom of an L-histidine residue with a halogen atom." [PubMed:18688235]
-synonym: "HalHis" EXACT PSI-MOD-label []
-property_value: Origin "H" xsd:string
-is_a: MOD:00694
-is_a: MOD:00909
-
-[Term]
-id: MOD:01050
-name: pyridyl alanyl
-def: "modification from DeltaMass" [DeltaMass:180]
-comment: From DeltaMass: Average Mass: 148 Formula:C8H8O2N1 Monoisotopic Mass Change:148.064 Average Mass Change:148.165
-property_value: Origin "A" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:01051
-name: 2-nitrobenzoyl
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 149
-synonym: "NBz" EXACT DeltaMass-label []
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-
-[Term]
-id: MOD:01052
-name: dimethoxybenzyl Trp
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 150
-property_value: Origin "W" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:01053
-name: 2-nitrophenylsulphenyl
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 153
-synonym: "Nps" EXACT DeltaMass-label []
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-
-[Term]
-id: MOD:01054
-name: 4-toluenesulfonyl
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 154
-synonym: "4-toluenesulphonyl" EXACT DeltaMass-label []
-synonym: "Tos" EXACT DeltaMass-label []
-synonym: "Tosyl" EXACT DeltaMass-label []
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-
-[Term]
-id: MOD:01055
-name: 3-nitro-2-pyridinesulfenyl
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 154
-synonym: "Npys" EXACT DeltaMass-label []
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-
-[Term]
-id: MOD:01056
-name: (79)Br labeled 3',5'-dibromotyrosine
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 156
-property_value: DiffAvg "155.82" xsd:float
-property_value: DiffFormula "(79)Br 2 C 0 H -2 N 0 O 0" xsd:string
-property_value: DiffMono "155.821024" xsd:float
-property_value: Formula "(79)Br 2 C 9 H 7 N 1 O 2" xsd:string
-property_value: MassAvg "318.88" xsd:float
-property_value: MassMono "318.884353" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-relationship: derives_from MOD:01023
-is_a: MOD:01006
-
-[Term]
-id: MOD:01057
-name: (79)Br and (81)Br labeled 3',5'-dibromotyrosine
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 158
-property_value: DiffAvg "157.82" xsd:float
-property_value: DiffFormula "(79)Br 1 (81)Br 1 C 0 H -2 N 0 O 0" xsd:string
-property_value: DiffMono "157.818978" xsd:float
-property_value: Formula "(79)Br 1 (81)Br 1 C 9 H 7 N 1 O 2" xsd:string
-property_value: MassAvg "320.88" xsd:float
-property_value: MassMono "320.882306" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-relationship: derives_from MOD:01023
-is_a: MOD:01006
-
-[Term]
-id: MOD:01058
-name: dichlorobenzyl
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 159
-synonym: "Dcb" EXACT DeltaMass-label []
-property_value: Source "artifact" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:01059
-name: (81)Br labeled 3',5'-dibromotyrosine
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 160
-property_value: DiffAvg "159.82" xsd:float
-property_value: DiffFormula "(81)Br 2 C 0 H -2 N 0 O 0" xsd:string
-property_value: DiffMono "159.816931" xsd:float
-property_value: Formula "(81)Br 2 C 9 H 7 N 1 O 2" xsd:string
-property_value: MassAvg "322.88" xsd:float
-property_value: MassMono "322.880260" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-relationship: derives_from MOD:01023
-is_a: MOD:01006
-
-[Term]
-id: MOD:01060
-name: S-carboxamidomethyl-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-carboxamidomethyl-L-cysteine." [DeltaMass:196, DeltaMass:337, OMSSA:3, PubMed:10504701, PubMed:11510821, PubMed:12422359, PubMed:18306178, Unimod:4#C]
-comment: From DeltaMass: (name misspelled \"Carboxyamidomethyl Cystenyl\") [JSG].
-subset: PSI-MOD-slim
-synonym: "amidocarboxymethylcysteine" EXACT DeltaMass-label []
-synonym: "CamC" EXACT PSI-MOD-alternate []
-synonym: "CamCys" EXACT DeltaMass-label []
-synonym: "Carbamidomethyl" RELATED PSI-MS-label []
-synonym: "carbamidomethylc" EXACT OMSSA-label []
-synonym: "carbamoylmethylcysteine" EXACT DeltaMass-label []
-synonym: "Carboxamidomethyl (on Cysteine)" EXACT DeltaMass-label []
-synonym: "Carboxyamidomethyl Cystenyl" EXACT DeltaMass-label []
-synonym: "Iodoacetamide derivative" RELATED Unimod-description []
-synonym: "S-carbamoylmethyl-L-cysteine" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "57.05" xsd:float
-property_value: DiffFormula "C 2 H 3 N 1 O 1 S 0" xsd:string
-property_value: DiffMono "57.021464" xsd:float
-property_value: Formula "C 5 H 8 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "160.19" xsd:float
-property_value: MassMono "160.030649" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:4
-is_a: MOD:00397
-is_a: MOD:00905
-
-[Term]
-id: MOD:01061
-name: S-carboxymethyl-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-carboxymethyl-L-cysteine." [DeltaMass:0, DeltaMass:197, OMSSA:2, Unimod:6#C]
-comment: From DeltaMass with no citation, name misspelled \"Carboxymethyl Cystenyl\", and formula incorrect, N and O reversed: Average Mass: 161 Abbreviation: -Cmc- Formula: C5H7O1N3S1 Monoisotopic Mass Change: 161.015 Average Mass Change: 161.179 [JSG].
-subset: PSI-MOD-slim
-synonym: "Carboxymethyl" RELATED PSI-MS-label []
-synonym: "Carboxymethyl cysteine" EXACT DeltaMass-label []
-synonym: "Carboxymethyl Cystenyl" EXACT DeltaMass-label []
-synonym: "carboxymethylc" EXACT OMSSA-label []
-synonym: "CmC" EXACT PSI-MOD-alternate []
-synonym: "Iodoacetic acid derivative" RELATED Unimod-description []
-property_value: DiffAvg "58.04" xsd:float
-property_value: DiffFormula "C 2 H 2 N 0 O 2 S 0" xsd:string
-property_value: DiffMono "58.005479" xsd:float
-property_value: Formula "C 5 H 7 N 1 O 3 S 1" xsd:string
-property_value: MassAvg "161.18" xsd:float
-property_value: MassMono "161.014664" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:6
-is_a: MOD:00399
-is_a: MOD:00905
-
-[Term]
-id: MOD:01062
-name: carboxymethyl cysteinyl
-def: "OBSOLETE because duplicate and redundant with MOD:01061. Remap to MOD:01061" [DeltaMass:197]
-comment: From DeltaMass:197 (Name misspelled \"cystenyl\", and formula incorrect, N and O reversed) Abbreviation:-Cmc- Formula:C5H7O1N3S1 Monoisotopic Mass Change:161.015 Average Mass Change:161.179
-synonym: "Carboxymethyl Cystenyl" EXACT DeltaMass-label []
-property_value: Formula "C 5 H 7 N 3 O 1 S 1" xsd:string
-property_value: MassAvg "157.19" xsd:float
-property_value: MassMono "157.030983" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-replaced_by: MOD:01061
-is_obsolete: true
-
-[Term]
-id: MOD:01063
-name: monomethylated phenylalanine
-def: "A protein modification that effectively converts an L-phenylalanine residue to a monomethylated phenylalanine." [DeltaMass:198]
-comment: From DeltaMass: Average Mass: 161 Formula: C10H11O1N1 Monoisotopic Mass Change: 161.084 Average Mass Change: 161.205. No citation provided. It is not obvious whether the DeltaMass entry is supposed to represent N-methylphenylalanine, alpha-methylphenylalanine, 2'-, 3'-, or 4'-methylphenylalanine [JSG].
-subset: PSI-MOD-slim
-synonym: "NMePhe" EXACT PSI-MOD-label []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 10 H 11 N 1 O 1" xsd:string
-property_value: MassAvg "161.20" xsd:float
-property_value: MassMono "161.084064" xsd:float
-property_value: Origin "F" xsd:string
-is_a: MOD:00599
-is_a: MOD:00717
-
-[Term]
-id: MOD:01064
-name: inositol
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 162
-is_a: MOD:00947
-
-[Term]
-id: MOD:01065
-name: hexose glycated N-terminal
-def: "A modification produced in a non-enzymatic reaction between a carbohydrate carbonyl group (C1 of aldohexose or C2 of fructose) and a protein N-terminal amino group to form a Schiff-base or an Amadori ketosamine  (or aminoketose) residue adduct." [DeltaMass:0, Unimod:41#N-term]
-comment: From DeltaMass: Average Mass: 162
-property_value: DiffAvg "162.14" xsd:float
-property_value: DiffFormula "C 6 H 10 O 5" xsd:string
-property_value: DiffMono "162.052823" xsd:float
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:41
-is_a: MOD:00767
-
-[Term]
-id: MOD:01066
-name: halogenated phenylalanine
-def: "A protein modification that effectively substitutes a hydrogen atom of an L-phenylalanine residue with a halogen atom." [PubMed:18688235]
-synonym: "HalPhe" EXACT PSI-MOD-label []
-property_value: Origin "F" xsd:string
-is_a: MOD:00694
-is_a: MOD:00914
-
-[Term]
-id: MOD:01067
-name: linker attached to peptide in Fmoc peptide synthesis
-def: "modification from DeltaMass" [DeltaMass:341]
-comment: From DeltaMass: Average Mass: 162 Average Mass Change:162 Notes: (from the ABRF discussion list archive) There may be ... things in the reagent K that would allow cleavage of the peptide to occur at the wrong place...in this case it removes the dimethoxybenzyl group first inactivating that site for cleavage, and it goes after tne next amide bond closer to the resin. Try the TFA/TIS/water/EDT cocktail...TFA = 92%, TIS =3%, and water is at 5%. .. had this issue on longer peptides.. and by increasing the amount of water a little bit... able to elminate this problem.
-property_value: Source "artifact" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:01068
-name: halogenated tryptophan
-def: "A protein modification that effectively substitutes a hydrogen atom of an L-tryptophan residue with a halogen atom." [PubMed:18688235]
-synonym: "HalTrp" EXACT PSI-MOD-label []
-property_value: Origin "W" xsd:string
-is_a: MOD:00694
-is_a: MOD:00918
-
-[Term]
-id: MOD:01069
-name: 2,4-dinitrophenyl modified residue
-def: "A protein modification that effectively substitutes a 2,4-dinitrophenyl group for a hydrogen atom." [DeltaMass:0]
-synonym: "Dnp" EXACT DeltaMass-label []
-property_value: DiffAvg "166.09" xsd:float
-property_value: DiffFormula "C 6 H 2 N 2 O 4" xsd:string
-property_value: DiffMono "166.001457" xsd:float
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-
-[Term]
-id: MOD:01070
-name: pentafluorophenyl modified residue
-def: "A protein modification that effectively substitutes a pentafluorophenyl group for a hydrogen atom." [DeltaMass:0]
-comment: From DeltaMass: name mispelled \"pentaflourophenyl\"
-synonym: "Pfp" EXACT DeltaMass-label []
-property_value: DiffAvg "166.05" xsd:float
-property_value: DiffFormula "C 6 F 5 H -1" xsd:string
-property_value: DiffMono "165.984191" xsd:float
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-
-[Term]
-id: MOD:01071
-name: diphenylmethyl modified residue
-def: "A protein modification that effectively substitutes a diphenylmethyl group for a hydrogen atom." [DeltaMass:0]
-synonym: "Dpm" EXACT DeltaMass-label []
-property_value: DiffAvg "166.22" xsd:float
-property_value: DiffFormula "C 13 H 10" xsd:string
-property_value: DiffMono "166.078250" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-
-[Term]
-id: MOD:01072
-name: monopotassium salt
-def: "A protein modification that effectively substitutes one potassium atom for one hydrogen atom." [DeltaMass:0]
-subset: PSI-MOD-slim
-synonym: "K1Res" EXACT PSI-MOD-label []
-property_value: DiffAvg "38.09" xsd:float
-property_value: DiffFormula "H -1 K 1" xsd:string
-property_value: DiffMono "37.955882" xsd:float
-property_value: Origin "X" xsd:string
-is_a: MOD:00849
-
-[Term]
-id: MOD:01073
-name: 2-chlorobenzyloxycarbonyl modified residue
-def: "A protein modification that effectively substitutes a 2-chlorobenzyloxycarbonyl group for a hydrogen atom." [DeltaMass:0]
-synonym: "Clz" EXACT DeltaMass-label []
-property_value: DiffAvg "169.58" xsd:float
-property_value: DiffFormula "C 8 Cl 1 H 6 O 2" xsd:string
-property_value: DiffMono "169.005632" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-
-[Term]
-id: MOD:01074
-name: napthylacetyl modified residue
-def: "A protein modification that effectively substitutes a napthylacetyl group for a hydrogen atom." [DeltaMass:0]
-property_value: DiffAvg "169.20" xsd:float
-property_value: DiffFormula "C 12 H 9 O 1" xsd:string
-property_value: DiffMono "169.065340" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-
-[Term]
-id: MOD:01075
-name: mercury containing modified residue
-def: "A protein modification that effectively substitutes a mercury atom or a cluster containing mercury for hydrogen atoms, or that coordinates a mercury ion." [PubMed:18688235]
-synonym: "HgRes" EXACT PSI-MOD-label []
-is_a: MOD:00698
-
-[Term]
-id: MOD:01076
-name: N-methyl arginyl
-def: "modification from DeltaMass - OBSOLETE because redundant and identical to MOD:00414. Remap to MOD:00414." [DeltaMass:215]
-comment: From DeltaMass: Average Mass: 170 Formula:C7H14O4N1 Monoisotopic Mass Change:170.117 Average Mass Change:170.215
-property_value: Formula "C 7 H 14 N 4 O 1" xsd:string
-property_value: MassAvg "170.22" xsd:float
-property_value: MassMono "170.116761" xsd:float
-property_value: Origin "R" xsd:string
-replaced_by: MOD:00414
-is_obsolete: true
-
-[Term]
-id: MOD:01077
-name: ethanedithiol/TFA cyclic adduct
-def: "modification from DeltaMass" [DeltaMass:216]
-comment: From DeltaMass: Average Mass: 172 Average Mass Change:172 References:[1]. Sieber,P.(1987) Modification of tryptophan residues during acidolysis of4-methoxy-2,3,6-trimethylbenzenesulfonyl groups. Effects of scavengers. Tetrahedron Lett., 28(15),1637-1640. Notes: TFA-cyclic dithioketal by-product is formed when Trp-containing peptide is subjected to prolonged TFA/EDT treatment [1]. See structure at http://www.abrf.org/images/misc/dmass172.gif. Additional discussion of this adduct, and how to avoid it, can befound in Methods in Enzymology 289, 67 (1997)
-property_value: Source "artifact" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:01078
-name: S-(2-aminoethyl)-3-methylcysteine (Thr)
-def: "A protein modification that effectively converts an L-threonine residue to S-(2-aminoethyl)-3-methylcysteine." [PubMed:12923550, Unimod:472#T]
-comment: From DeltaMass: Average Mass: 146 Abbreviation:-AECys_ Formula:C5H10O2N1S1 Monoisotopic Mass Change:146.051 Average Mass Change:146.214 References:PE Sciex.
-synonym: "2-amino-3-(2-aminoethyl)sulfanyl-3-methylbutanoic acid" EXACT PSI-MOD-alternate []
-synonym: "AEC-MAEC" RELATED Unimod-interim []
-synonym: "beta-methylaminoethylcysteine" RELATED Unimod-description []
-synonym: "S-aminoethyl-3-methylcysteine" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "59.13" xsd:float
-property_value: DiffFormula "C 2 H 5 N 1 O -1 S 1" xsd:string
-property_value: DiffMono "59.019356" xsd:float
-property_value: Formula "C 6 H 12 N 2 O 1 S 1" xsd:string
-property_value: MassAvg "160.24" xsd:float
-property_value: MassMono "160.067034" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:472
-is_a: MOD:00917
-
-[Term]
-id: MOD:01079
-name: S-(acetylamino)methyl-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-[(acetylamino)methyl]-L-cysteine." [DeltaMass:218, PubMed:8572278]
-comment: From DeltaMass: (name misspelled \"Acetamidomethyl Cystenyl\") Average Mass: 174 Formula: C 6 H 10 O 2 N 2 S 1 Monoisotopic Mass Change: 174.046 Average Mass Change: 174.221. [These are aggregate masses, not delta masses.] See Organic Syntheses, Coll. Vol. 6, p.5 (1988); Vol. 59, p.190 (1979); http://www.orgsyn.org/orgsyn/orgsyn/prepContent.asp?prep=cv6p0005 [JSG].
-synonym: "Acetamidomethyl Cystenyl" EXACT DeltaMass-label []
-synonym: "Acm-Cys" EXACT PSI-MOD-alternate []
-synonym: "N-(hydroxymethyl)acetamide derivatized L-cysteine" EXACT PSI-MOD-alternate []
-synonym: "S-(acetamido)methyl-L-cysteine" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "71.08" xsd:float
-property_value: DiffFormula "C 3 H 5 N 1 O 1 S 0" xsd:string
-property_value: DiffMono "71.037114" xsd:float
-property_value: Formula "C 6 H 10 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "174.22" xsd:float
-property_value: MassMono "174.046299" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-is_a: MOD:00905
-
-[Term]
-id: MOD:01080
-name: acrylamidyl cysteinyl
-def: "OBSOLETE because this is identical to MOD:00417.  modification from DeltaMass" [DeltaMass:219]
-comment: From DeltaMass: (name misspelled \"Acrylamidyl Cystenyl\") Average Mass: 174 Formula: C6H10O2N2S1 Monoisotopic Mass Change: 174.046 Average Mass Change: 174.221
-synonym: "Acrylamidyl Cystenyl" EXACT DeltaMass-label []
-property_value: Formula "C 6 H 10 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "174.22" xsd:float
-property_value: MassMono "174.046299" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-replaced_by: MOD:00417
-is_obsolete: true
-
-[Term]
-id: MOD:01081
-name: delta-glycosyloxy- (of lysine) or beta-glycosyloxy- (of phenylalanine or tyrosine)
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 177. CAUTION - mass does not match formula.
-property_value: DiffAvg "178.14" xsd:float
-property_value: DiffFormula "C 6 H 10 O 6" xsd:string
-property_value: DiffMono "178.047738" xsd:float
-is_a: MOD:00947
-
-[Term]
-id: MOD:01082
-name: 4-glycosyloxy- (hexosyl, C6) (of proline)
-def: "OBSOLETE because redundant with MOD:00757, remap. modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 177. Caution: Formula does not match mass. The natural glycosylating sugar of hydroxyproline is galactose.
-property_value: DiffAvg "178.14" xsd:float
-property_value: DiffFormula "C 6 H 10 O 6" xsd:string
-property_value: DiffMono "178.047738" xsd:float
-property_value: Formula "C 11 H 17 N 1 O 6" xsd:string
-property_value: MassAvg "259.26" xsd:float
-property_value: MassMono "259.105587" xsd:float
-property_value: Origin "P" xsd:string
-replaced_by: MOD:00757
-is_obsolete: true
-
-[Term]
-id: MOD:01083
-name: O-benzyl-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O-benzyl-L-serine." [DeltaMass:0]
-property_value: DiffAvg "90.13" xsd:float
-property_value: DiffFormula "C 7 H 6" xsd:string
-property_value: DiffMono "90.046950" xsd:float
-property_value: Formula "C 10 H 11 N 1 O 2" xsd:string
-property_value: MassAvg "177.20" xsd:float
-property_value: MassMono "177.078979" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00916
-is_a: MOD:01008
-
-[Term]
-id: MOD:01084
-name: iodoacetic acid derivatized amino-terminal residue
-def: "A protein modification that by reaction of iodoacetic acid effectively replaces a residue alpha-amino- or alpha-imino-hydrogen with a carboxymethyl group." [Unimod:6#N-term]
-subset: PSI-MOD-slim
-synonym: "Carboxymethyl" RELATED PSI-MS-label []
-synonym: "Carboxymethyl (on Cysteine)" EXACT DeltaMass-label []
-synonym: "Iodoacetic acid derivative" RELATED Unimod-description []
-property_value: DiffAvg "58.04" xsd:float
-property_value: DiffFormula "C 2 H 2 O 2" xsd:string
-property_value: DiffMono "58.005479" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:6
-is_a: MOD:00399
-
-[Term]
-id: MOD:01085
-name: alpha-N-gluconoylated L-histidine
-def: "A protein modification that effectively replaces the N-terminal hydrogen atom of a N-terminal histidine residue with a gluconoyl group linked through a glycosidic bond. modification from DeltaMass" [PubMed:9918669, DeltaMass:226]
-comment: Occurs on His-tagged proteins expresssed in E. coli. From DeltaMass: Average Mass: 178 Formula: C6H10O6 Monoisotopic Mass Change: 178.05 Average Mass Change: 178.14 References: Geoghegan, K. F., H. B. Dixon, et al. (1999). Spontaneous alpha-N-6-phosphogluconoylation of a His tag in Escherichia coli: the cause of extra mass of 258 or 178 Da in fusion proteins. Anal Biochem 267(1): 169-84. Mass listed here is 179 because it's N-terminal.
-property_value: DiffAvg "179.15" xsd:float
-property_value: DiffFormula "C 6 H 11 O 6" xsd:string
-property_value: DiffMono "179.055563" xsd:float
-property_value: Formula "C 12 H 18 N 3 O 7" xsd:string
-property_value: MassAvg "316.29" xsd:float
-property_value: MassMono "316.114475" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00909
-is_a: MOD:00006
-
-[Term]
-id: MOD:01086
-name: p-nitrobenzyloxycarbonyl
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 179
-synonym: "4Nz" EXACT DeltaMass-label []
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-
-[Term]
-id: MOD:01087
-name: 2,4,5-trichlorophenyl modified residue
-def: "A protein modification that effectively substitutes a 2,4,5-trichlorophenyl group for a hydrogen atom." [DeltaMass:0]
-property_value: DiffAvg "179.42" xsd:float
-property_value: DiffFormula "C 6 Cl 3 H 1" xsd:string
-property_value: DiffMono "177.914383" xsd:float
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-
-[Term]
-id: MOD:01088
-name: 2,4,6-trimethyloxybenzyl modified residue
-def: "A protein modification that effectively substitutes a 2,4,6-trimethyloxybenzyl group for a hydrogen atom." [DeltaMass:0]
-synonym: "Tmob" EXACT DeltaMass-label []
-property_value: DiffAvg "180.20" xsd:float
-property_value: DiffFormula "C 10 H 12 O 3" xsd:string
-property_value: DiffMono "180.078644" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-
-[Term]
-id: MOD:01089
-name: xanthyl
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 180
-synonym: "Xan" EXACT DeltaMass-label []
-property_value: Source "artifact" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:01090
-name: iodoacetamide derivatized amino-terminal residue
-def: "A protein modification that by reaction of iodoacetamide effectively replaces a residue alpha-amino- or alpha-imino-hydrogen with a carboxamidomethyl group." [PubMed:11327326, PubMed:11510821, PubMed:12422359, Unimod:4#N-term]
-subset: PSI-MOD-slim
-synonym: "(carbamoylmethyl)amino" EXACT PSI-MOD-alternate []
-synonym: "Carbamidomethyl" RELATED PSI-MS-label []
-synonym: "Iodoacetamide derivative" RELATED Unimod-description []
-property_value: DiffAvg "57.05" xsd:float
-property_value: DiffFormula "C 2 H 3 N 1 O 1" xsd:string
-property_value: DiffMono "57.021464" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:4
-is_a: MOD:00397
-
-[Term]
-id: MOD:01091
-name: monochlorinated L-phenylalanine
-def: "A protein modification that effectively substitutes one hydrogen atom of an L-phenylalanine residue with one chlorine atom." [DeltaMass:233]
-comment: From DeltaMass: Average Mass: 182 Formula:C9H8O1N1Cl1 Monoisotopic Mass Change:181.029 Average Mass Change:181.623
-synonym: "Cl1Phe" EXACT PSI-MOD-label []
-property_value: DiffAvg "34.44" xsd:float
-property_value: DiffFormula "C 0 Cl 1 H -1 N 0 O 0" xsd:string
-property_value: DiffMono "33.961028" xsd:float
-property_value: Formula "C 9 Cl 1 H 8 N 1 O 1" xsd:string
-property_value: MassAvg "181.62" xsd:float
-property_value: MassMono "181.029442" xsd:float
-property_value: Origin "F" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01066
-is_a: MOD:01911
-
-[Term]
-id: MOD:01092
-name: mesitylene-2-sulfonyl
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 182
-synonym: "Mts" EXACT DeltaMass-label []
-property_value: Source "artifact" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:01093
-name: isopropyl lysyl
-def: "modification from DeltaMass" [DeltaMass:236]
-comment: From DeltaMass: Average Mass: 184 Formula: C9H16O2N2 Monoisotopic Mass Change: 184.12 Average Mass Change: 184.24 with no citation.
-property_value: Formula "C 9 H 16 N 2 O 2" xsd:string
-property_value: MassAvg "184.24" xsd:float
-property_value: MassMono "184.121178" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:01094
-name: N6-carboxymethyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-carboxymethyl-L-lysine." [DeltaMass:237, Unimod:6#K]
-comment: From DeltaMass:237 (with no citation, formula incorrect, N and O reversed) Average Mass: 186 Formula: C8H14O2N3 Monoisotopic Mass Change: 186.1 Average Mass Change: 186.211 [JSG].
-subset: PSI-MOD-slim
-synonym: "Carboxymethyl" RELATED PSI-MS-label []
-synonym: "Carboxymethyl Lysyl" EXACT DeltaMass-label []
-synonym: "Iodoacetic acid derivative" RELATED Unimod-description []
-property_value: DiffAvg "58.04" xsd:float
-property_value: DiffFormula "C 2 H 2 O 2" xsd:string
-property_value: DiffMono "58.005479" xsd:float
-property_value: Formula "C 8 H 14 N 2 O 3" xsd:string
-property_value: MassAvg "186.21" xsd:float
-property_value: MassMono "186.100442" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:6
-is_a: MOD:00399
-
-[Term]
-id: MOD:01095
-name: Matrix alpha cyano MH+
-def: "Modification from DeltaMass. OBSOLETE because not an amino acid modification." [DeltaMass:240]
-comment: From DeltaMass with no citation, formula incorrect, N and O reversed: Formula: C10H8O1N3 Monoisotopic Mass Change: 190.05 Average Mass Change: 190.18.
-property_value: Formula "C 10 H 8 N 1 O 3" xsd:string
-property_value: MassAvg "190.18" xsd:float
-property_value: MassMono "190.050418" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_obsolete: true
-
-[Term]
-id: MOD:01096
-name: O-benzyl-L-threonine
-def: "A protein modification that effectively converts an L-threonine residue to O-benzyl-L-threonine." [DeltaMass:0]
-property_value: DiffAvg "90.13" xsd:float
-property_value: DiffFormula "C 7 H 6" xsd:string
-property_value: DiffMono "90.046950" xsd:float
-property_value: Formula "C 11 H 13 N 1 O 2" xsd:string
-property_value: MassAvg "191.23" xsd:float
-property_value: MassMono "191.094629" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00917
-is_a: MOD:01008
-
-[Term]
-id: MOD:01097
-name: S-benzyl-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-benzyl-L-cysteine." [DeltaMass:242]
-comment: From DeltaMass: misspelled \"Benzyl Cystenyl\".
-property_value: DiffAvg "90.13" xsd:float
-property_value: DiffFormula "C 7 H 6" xsd:string
-property_value: DiffMono "90.046950" xsd:float
-property_value: Formula "C 10 H 11 N 1 O 1 S 1" xsd:string
-property_value: MassAvg "193.26" xsd:float
-property_value: MassMono "193.056135" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00905
-is_a: MOD:01008
-
-[Term]
-id: MOD:01098
-name: naphthylalanine residue
-def: "A protein modification that inserts or replaces a residue with a naphthylalanine." [DeltaMass:243]
-comment: From DeltaMass: Average Mass: 197 Formula: C13H11O1N1 Monoisotopic Mass Change: 197.084 Average Mass Change: 197.238. No citation provided. It is not obvious which isomer of naphthylalanine this DeltaMass entry is supposed to represent [JSG].
-property_value: Formula "C 13 H 11 N 1 O 1" xsd:string
-property_value: MassAvg "197.24" xsd:float
-property_value: MassMono "197.084064" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00850
-
-[Term]
-id: MOD:01099
-name: succinyl beta-aspartyl anhydride
-def: "A protein modification that effectively converts an L-aspartic acid residue to succinyl beta-aspartyl anhydride." [DeltaMass:244]
-comment: From DeltaMass with no citation (name misspelled \"aspartamyl\", and formula incorrect, N and O reversed) Average Mass: 198 Formula: C8H8O1N5 Monoisotopic Mass Change: 198.04 Average Mass Change: 198.156 [JSG].
-synonym: "succinyl aspartamyl" EXACT DeltaMass-label []
-property_value: DiffAvg "82.06" xsd:float
-property_value: DiffFormula "C 4 H 2 N 0 O 2" xsd:string
-property_value: DiffMono "82.005479" xsd:float
-property_value: Formula "C 8 H 8 N 1 O 5" xsd:string
-property_value: MassAvg "198.15" xsd:float
-property_value: MassMono "198.040247" xsd:float
-property_value: Origin "D" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00904
-
-[Term]
-id: MOD:01100
-name: HMP (hydroxymethylphenyl)/TFA adduct
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 201 with no citation.
-property_value: Source "artifact" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:01101
-name: S-Farnesyl-
-def: "OBSOLETE because erroneous and apparently redundant to MOD:00111. Remap to MOD:00111." [DeltaMass:0]
-comment: Modification from DeltaMass: Average Mass: 206. This entry with no other information available appears to be the same as the entry at 204 for \"Farnesylation\" but with an incorrect mass.
-replaced_by: MOD:00111
-is_obsolete: true
-
-[Term]
-id: MOD:01102
-name: myristoylation-4H (two double bonds)
-def: "OBSOLETE because redundant and identical to MOD:00504. Remap to MOD:00504." [DeltaMass:348]
-comment: From DeltaMass: Average Mass: 206 Formula: C14 H22 O1 Monoisotopic Mass Change: 206.167 Average Mass Change: 206.324 References: Neubert TA, Johnson RS, Hurley JB, Walsh KA (1992). The rod transducin alpha subunit amino terminus is heterogeneously fatty acylated. J Biol Chem. 267(26), 18274-7. Notes: Modification of protein N-terminus with (cis,cis-delta 5, delta 8)-tetradecadienoyl group (myristoylation with 2 double bonds)
-property_value: Source "natural" xsd:string
-replaced_by: MOD:00504
-is_obsolete: true
-
-[Term]
-id: MOD:01103
-name: myristoleylation (one double bond)
-def: "OBSOLETE because redundant and identical to MOD:00503. Remap to MOD:00503." [DeltaMass:0]
-comment: From DeltaMass with no citation or formula: Average Mass: 208.
-property_value: Source "natural" xsd:string
-replaced_by: MOD:00503
-is_obsolete: true
-
-[Term]
-id: MOD:01104
-name: 4-methoxy-2,3,6-trimethylbenzenesulfonyl
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 212 with no citation.
-synonym: "Mtr" EXACT DeltaMass-label []
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-
-[Term]
-id: MOD:01105
-name: 2-bromobenzyloxycarbonyl
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 213 with no citation.
-synonym: "BrZ" EXACT DeltaMass-label []
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-
-[Term]
-id: MOD:01106
-name: N-formyl-L-tryptophan
-def: "A protein modification that effectively converts an L-tryptophan residue to N-formyl-L-tryptophan." [DeltaMass:0]
-comment: From DeltaMass with no citation or formula: Average Mass: 214. It is not clear what this is supposed to represent. The mass corresponds to an N-formyl tryptophan (either N2 or N1'), but neither of these modifications has been reported as commonly encountered. It may have been confused with N'-formyl-L-kynurenine, see MOD:00464 [JSG]
-synonym: "formyl tryptophanyl" EXACT DeltaMass-label []
-property_value: DiffAvg "28.01" xsd:float
-property_value: DiffFormula "C 1 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "27.994915" xsd:float
-property_value: Formula "C 12 H 10 N 2 O 2" xsd:string
-property_value: MassAvg "214.22" xsd:float
-property_value: MassMono "214.074228" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00409
-is_a: MOD:00918
-
-[Term]
-id: MOD:01107
-name: O5-benzyl-L-glutamate
-def: "A protein modification that effectively converts an L-glutamic acid residue to O5-benzyl-L-glutamate." [DeltaMass:258]
-comment: From DeltaMass with no citation: (formula incorrect, N and O reversed; mass incorrect, aggregate not delta) Average Mass: 219 Formula: C12H13O1N3 Monoisotopic Mass Change: 219.241 Average Mass Change: 219.09 [JSG].
-property_value: DiffAvg "90.13" xsd:float
-property_value: DiffFormula "C 7 H 6" xsd:string
-property_value: DiffMono "90.046950" xsd:float
-property_value: Formula "C 12 H 13 N 1 O 3" xsd:string
-property_value: MassAvg "219.24" xsd:float
-property_value: MassMono "219.089543" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00906
-is_a: MOD:01008
-
-[Term]
-id: MOD:01108
-name: 2-amino-5-(4-methoxyphenyl)-5-oxopentanoic acid (Glu)
-def: "A protein modification that effectively converts an L-glutamic acid residue to 2-amino-5-(4-methoxyphenyl)-5-oxopentanoic acid, glutamtic acid anisole adduct." [DeltaMass:259]
-comment: From DeltaMass with no citation: (formula incorrect, N and O reversed; mass incorrect, aggregate not delta) Average Mass: 219 Formula: C12H13O1N3 Monoisotopic Mass Change: 219.241 Average Mass Change: 219.09 [JSG].
-synonym: "anisole adducted glutamyl" EXACT DeltaMass-label []
-property_value: DiffAvg "90.13" xsd:float
-property_value: DiffFormula "C 7 H 6" xsd:string
-property_value: DiffMono "90.046950" xsd:float
-property_value: Formula "C 12 H 13 N 1 O 3" xsd:string
-property_value: MassAvg "219.24" xsd:float
-property_value: MassMono "219.089543" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00906
-is_a: MOD:01007
-
-[Term]
-id: MOD:01109
-name: 9-fluorenylmethyloxycarbonyl (Fmoc)
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 222 with no citation.
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-
-[Term]
-id: MOD:01110
-name: isoprenylated cysteine
-def: "A protein modification that effectively replaces a hydrogen atom of an L-cysteine residue with a group derived from an isoprene polymer, such as a geranyl (C10), farnesyl (C15) or geranylgeranyl (C20)." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "IpCys" EXACT PSI-MOD-label []
-property_value: Origin "C" xsd:string
-is_a: MOD:00703
-is_a: MOD:00905
-
-[Term]
-id: MOD:01111
-name: dimethoxybenzhydryl modified residue
-def: "A protein modification that effectively substitutes a dimethoxybenzhydryl group for a hydrogen atom." [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 226 with no citation. A reagent, typically 4,4'-dimethoxybenzhydryl chloride, used as a protecting group for the carboxamido group of asparagine and glutamine during chemical peptide synthesis [JSG].
-synonym: "4,4'-dimethoxybenzhydryl" EXACT PSI-MOD-alternate []
-synonym: "bis(4-methoxyphenyl)methyl" EXACT PSI-MOD-alternate []
-synonym: "Mbh" EXACT DeltaMass-label []
-property_value: DiffAvg "226.27" xsd:float
-property_value: DiffFormula "C 15 H 14 O 2" xsd:string
-property_value: DiffMono "226.099380" xsd:float
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-
-[Term]
-id: MOD:01112
-name: nicotinoyl lysine
-def: "modification from DeltaMass" [DeltaMass:266]
-comment: From DeltaMass: (name misspelled \"nicotinyl\"; formula incorrect, N and O reversed; mass incorrect, aggregate not delta) Average Mass: 233 Formula: C12H15O3N2 Monoisotopic Mass Change: 233.116 Average Mass Change: 233.271
-synonym: "nicotinyl lysyl" EXACT DeltaMass-label []
-property_value: DiffAvg "105.10" xsd:float
-property_value: DiffFormula "C 6 H 3 N 1 O 1" xsd:string
-property_value: DiffMono "105.021464" xsd:float
-property_value: Formula "C 12 H 15 N 3 O 2" xsd:string
-property_value: MassAvg "233.27" xsd:float
-property_value: MassMono "233.116427" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:01113
-name: 2-(p-biphenyl)isopropyl-oxycarbonyl
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 238 with no citation.
-synonym: "Bpoc" EXACT DeltaMass-label []
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-
-[Term]
-id: MOD:01114
-name: triphenylmethyl
-def: "modification from DeltaMass" [DeltaMass:270]
-comment: From DeltaMass: Average Mass: 242 Average Mass Change: 242.3 Notes: blocking group used in peptide synthesis for C,H,Q,N
-synonym: "Trityl" EXACT DeltaMass-label []
-synonym: "Trt" EXACT DeltaMass-label []
-property_value: DiffAvg "242.32" xsd:float
-property_value: DiffFormula "C 19 H 14" xsd:string
-property_value: DiffMono "242.109550" xsd:float
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-
-[Term]
-id: MOD:01115
-name: isoprenylated tryptophan
-def: "A protein modification that effectively replaces a hydrogen atom of an L-tryptophan residue with a group derived from an isoprene polymer, such as a geranyl (C10), farnesyl (C15) or geranylgeranyl (C20)." [PubMed:18688235]
-synonym: "IpTrp" EXACT PSI-MOD-label []
-property_value: Origin "W" xsd:string
-is_a: MOD:00703
-is_a: MOD:00918
-
-[Term]
-id: MOD:01116
-name: S-farnesyl-L-cysteine methyl ester
-def: "A protein modification that effectively converts an L-cysteine residue to S-farnesyl-L-cysteine methyl ester." [PubMed:15609361, RESID:AA0102#var, RESID:AA0105#var]
-subset: PSI-MOD-slim
-synonym: "SFarnOMeCys" EXACT PSI-MOD-label []
-property_value: DiffAvg "218.38" xsd:float
-property_value: DiffFormula "C 16 H 26 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "218.203451" xsd:float
-property_value: Formula "C 19 H 32 N 1 O 2 S 1" xsd:string
-property_value: MassAvg "338.53" xsd:float
-property_value: MassMono "338.215375" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-is_a: MOD:00905
-relationship: has_functional_parent MOD:00111
-relationship: has_functional_parent MOD:00114
-
-[Term]
-id: MOD:01117
-name: pentamethyldihydrobenzofuransulfonyl
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 252 with no citation.
-synonym: "Pbf" EXACT DeltaMass-label []
-property_value: Source "artifact" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:01118
-name: alpha-N-6-phosphogluconoylated L-histidine
-def: "A protein modification that effectively replaces the N-terminal hydrogen atom of a N-terminal histidine residue with a 6-phosphogluconoyl group linked through a glycosidic bond. modification from DeltaMass" [PubMed:9918669, DeltaMass:275]
-comment: Occurs on His-tagged proteins expresssed in E. coli.From DeltaMass: Average Mass: 258 Formula: C6H10O6HPO3 Monoisotopic Mass Change: 258.01 Average Mass Change: 258.12 References: Geoghegan, K. F., H. B. Dixon, et al. (1999). Spontaneous alpha-N-6-phosphogluconoylation of a His tag in Escherichia coli: the cause of extra mass of 258 or 178 Da in fusion proteins. Anal Biochem 267(1): 169-84. Mass is one Da higher because this is an N-terminal modification
-property_value: DiffAvg "259.12" xsd:float
-property_value: DiffFormula "C 6 H 12 O 9 P 1" xsd:string
-property_value: DiffMono "259.021894" xsd:float
-property_value: Formula "C 12 H 19 N 3 O 10 P 1" xsd:string
-property_value: MassAvg "396.27" xsd:float
-property_value: MassMono "396.080806" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00909
-is_a: MOD:00006
-
-[Term]
-id: MOD:01119
-name: S-geranylgeranyl-L-cysteine methyl ester
-def: "A protein modification that effectively converts an L-cysteine residue to S-geranylgeranyl-L-cysteine methyl ester." [PubMed:1483450, PubMed:15609361, RESID:AA0104#var, RESID:AA0105#var]
-subset: PSI-MOD-slim
-synonym: "SGergerOMeCys" EXACT PSI-MOD-label []
-property_value: DiffAvg "286.50" xsd:float
-property_value: DiffFormula "C 21 H 34 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "286.266051" xsd:float
-property_value: Formula "C 24 H 40 N 1 O 2 S 1" xsd:string
-property_value: MassAvg "406.65" xsd:float
-property_value: MassMono "406.277976" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-is_a: MOD:00905
-relationship: has_functional_parent MOD:00113
-relationship: has_functional_parent MOD:00114
-
-[Term]
-id: MOD:01120
-name: 2,2,5,7,8-pentamethylchroman-6-sulfonyl chloride derivatized residue
-def: "A protein modification that is produced by formation of an adduct with 2,2,5,7,8-pentamethylchroman-6-sulfonyl chloride, Pmc chloride." [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 266 Notes: blocking group for Arg in peptide synthesis. CAS:112160-39-1 [JSG].
-synonym: "2,2,5,7,8-pentamethyl-3,4-dihydro-2H-chromene-6-sulfonyl" EXACT PSI-MOD-alternate []
-synonym: "2,2,5,7,8-pentamethyl-6-chromansulfonyl" EXACT PSI-MOD-alternate []
-synonym: "2,2,5,7,8-pentamethyl-chromane-6-sulfonyl" EXACT PSI-MOD-alternate []
-synonym: "2,2,5,7,8-pentamethylchroman-6-sulfonyl" EXACT PSI-MOD-alternate []
-synonym: "2,2,5,7,8-pentamethylchroman-6-sulphonyl" EXACT PSI-MOD-alternate []
-synonym: "3,4-dihydro-2,2,5,7,8-pentamethyl-2H-1-benzopyran-6-sulfonyl" EXACT PSI-MOD-alternate []
-synonym: "Pmc" EXACT DeltaMass-label []
-synonym: "PmcRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "266.36" xsd:float
-property_value: DiffFormula "C 14 H 18 O 3 S 1" xsd:string
-property_value: DiffMono "266.097665" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01652
-
-[Term]
-id: MOD:01121
-name: monomethoxytrityl
-def: "modification from DeltaMass" [DeltaMass:280]
-comment: From DeltaMass: Average Mass: 272 Average Mass Change: 272
-synonym: "Mmt" EXACT DeltaMass-label []
-property_value: Source "artifact" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:01122
-name: 5'phos dCytidinyl
-def: "OBSOLETE because this is a modification that occurs to DNA/RNA and not proteins. modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 289 with no citation.
-is_obsolete: true
-
-[Term]
-id: MOD:01123
-name: monoiodated tyrosine
-def: "OBSOLETE because redundant and identical to MOD:01123. Remap to MOD:01123." [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 289
-property_value: Origin "Y" xsd:string
-replaced_by: MOD:01123
-is_obsolete: true
-
-[Term]
-id: MOD:01124
-name: aldohexosyl lysyl
-def: "modification from DeltaMass" [DeltaMass:285]
-comment: From DeltaMass: (formula incorrect, N and O reversed; mass incorrect, aggregate not delta) Average Mass: 290 Formula: C12H22O2N6 Monoisotopic Mass Change: 290.148 Average Mass Change: 290.317
-property_value: DiffAvg "162.14" xsd:float
-property_value: DiffFormula "C 6 H 10 N 0 O 5" xsd:string
-property_value: DiffMono "162.052823" xsd:float
-property_value: Formula "C 12 H 22 N 2 O 6" xsd:string
-property_value: MassAvg "290.32" xsd:float
-property_value: MassMono "290.147786" xsd:float
-property_value: Origin "K" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:01125
-name: 5'phos dThymidinyl
-def: "OBSOLETE because this is a modification that occurs to DNA/RNA and not proteins. modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 304 with no citation.
-is_obsolete: true
-
-[Term]
-id: MOD:01126
-name: 5'phos Cytidinyl
-def: "OBSOLETE because this is a modification that occurs to DNA/RNA and not proteins. modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 305 with no citation.
-is_obsolete: true
-
-[Term]
-id: MOD:01127
-name: 5'phos Uridinyl
-def: "OBSOLETE because redundant and identical to MOD:01166. Remap to MOD:01166." [DeltaMass:292]
-comment: From DeltaMass: Average Mass: 306 Formula: C9H11O2N8P1 Monoisotopic Mass Change: 306.025 Average Mass Change: 306.17
-replaced_by: MOD:01166
-is_obsolete: true
-
-[Term]
-id: MOD:01128
-name: N-glycolneuraminic acid
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 307 with no citation.
-synonym: "NeuGc" EXACT DeltaMass-label []
-is_a: MOD:00947
-
-[Term]
-id: MOD:01129
-name: 5'phos dAdenosyl
-def: "OBSOLETE because this is a modification that occurs to DNA/RNA and not proteins. modification from DeltaMass" [DeltaMass:295]
-comment: From DeltaMass: Average Mass: 313 Formula: C10H12O5N5P1 Monoisotopic Mass Change: 313.058 Average Mass Change: 313.211
-is_obsolete: true
-
-[Term]
-id: MOD:01130
-name: SucPhencarb Lysyl
-def: "modification from DeltaMass" [DeltaMass:297]
-comment: From DeltaMass: Average Mass: 327 Formula: C17H17O3N4 Monoisotopic Mass Change: 327.122 Average Mass Change: 327.342
-property_value: Source "artifact" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:01131
-name: 5'phos dGuanosyl
-def: "OBSOLETE because this is a modification that occurs to DNA/RNA and not proteins. modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 329
-is_obsolete: true
-
-[Term]
-id: MOD:01132
-name: 5'phos Adenosinyl
-def: "OBSOLETE because redundant and identical to MOD:01165. Remap to MOD:01165." [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 329
-replaced_by: MOD:01165
-is_obsolete: true
-
-[Term]
-id: MOD:01133
-name: S-12-hydroxyfarnesyl-L-cysteine methyl ester
-def: "A protein modification that effectively converts an L-cysteine residue to S-12-hydroxyfarnesyl-L-cysteine methyl ester." [PubMed:17790543, RESID:AA0103#var, RESID:AA0105#var]
-synonym: "S12HyFarnOMeCys" EXACT PSI-MOD-label []
-property_value: DiffAvg "234.38" xsd:float
-property_value: DiffFormula "C 16 H 26 N 0 O 1 S 0" xsd:string
-property_value: DiffMono "234.198365" xsd:float
-property_value: Formula "C 19 H 32 N 1 O 3 S 1" xsd:string
-property_value: MassAvg "354.53" xsd:float
-property_value: MassMono "354.210290" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-is_a: MOD:00905
-relationship: has_functional_parent MOD:00112
-relationship: has_functional_parent MOD:00114
-
-[Term]
-id: MOD:01134
-name: fluorescein labelling of peptide N-terminal using NHS ester
-def: "modification from DeltaMass" [DeltaMass:306]
-comment: From DeltaMass: Average Mass: 359 Formula: C21H11O6 Monoisotopic Mass Change: 359.055 Average Mass Change: 359.315 Notes: Using the DHB matrix at low pH the carboxyl group and one of the oxygens on the flurorescein molecule are protinated so the delta mass is 2Da higher than most text book illustrations would indicate. See Bioconjugate Techniques by Greg Hermanson, Academic Press, page 305, figure 204. Text books of course just show the coupling reaction at neutral or basic pH.
-property_value: Source "artifact" xsd:string
-is_a: MOD:00947
-
-[Term]
-id: MOD:01135
-name: Hex-HexNAc
-def: "modification from DeltaMass" [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 365 with no citation.
-is_a: MOD:00947
-
-[Term]
-id: MOD:01136
-name: dioctyl phthalate
-def: "OBSOLETE because this is a small molecule contaminant and not a modification to a polypeptide. modification from DeltaMass" [DeltaMass:309]
-comment: From DeltaMass: Average Mass: 391 Average Mass Change: 391 Notes: A common plasticizer, and, unfortunaltely, a common contaminate. A sodium adduct is often associated with this peak at 413.
-property_value: Source "artifact" xsd:string
-is_obsolete: true
-
-[Term]
-id: MOD:01137
-name: N6-(2,2,5,7,8-pentamethylchroman-6-sulfonyl)-L-lysine
-def: "A protein modification that is produced by reaction of a lysine residue with 2,2,5,7,8-pentamethylchroman-6-sulfonyl chloride, Pmc chloride, to form N6-(2,2,5,7,8-pentamethylchroman-6-sulfonyl)-L-lysine." [DeltaMass:310]
-comment: From DeltaMass: Average Mass: Formula: C20H30O2N4S1 Monoisotopic Mass Change: 394.192 Average Mass Change: 394.534
-synonym: "PMC lysyl" EXACT DeltaMass-label []
-synonym: "PmcLys" EXACT PSI-MOD-label []
-property_value: DiffAvg "266.36" xsd:float
-property_value: DiffFormula "C 14 H 18 O 3 S 1" xsd:string
-property_value: DiffMono "266.097665" xsd:float
-property_value: Formula "C 20 H 30 N 2 O 4 S 1" xsd:string
-property_value: MassAvg "394.53" xsd:float
-property_value: MassMono "394.192628" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00902
-is_a: MOD:01120
-
-[Term]
-id: MOD:01138
-name: Aedans Cystenyl
-def: "OBSOLETE because no evidence has been seen for this protein modification. modification from DeltaMass" [DeltaMass:311]
-comment: [probably aminoethyldansyl, JSG] From DeltaMass: (name misspelled \"Aedans Cystenyl\", and formula incorrect, N and O reversed) Average Mass: 409 Abbreviation: Aedans-Cys Formula: C17H19O3N5S2 Monoisotopic Mass Change: 409.077 Average Mass Change: 409.482
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-is_obsolete: true
-
-[Term]
-id: MOD:01139
-name: dioctyl phthalate sodium adduct
-def: "OBSOLETE because this is a MS contaminant, not a known modification to a polypeptide. modification from DeltaMass" [DeltaMass:312]
-comment: From DeltaMass: Mass: Average Mass Change: 413 Notes: A common plasticizer, and, unfortunaltely, a common contaminate. A sodium adduct is often associated with this peak at 413.
-property_value: Source "artifact" xsd:string
-is_obsolete: true
-
-[Term]
-id: MOD:01140
-name: diiodinated tyrosine
-def: "A protein modification that effectively substitutes two hydrogen atoms of an L-tyrosine residue with two iodine atoms." [DeltaMass:0, OMSSA:35, PubMed:15627961, Unimod:130#Y]
-subset: PSI-MOD-slim
-synonym: "3,5-Diiodination (of Tyrosine)" EXACT DeltaMass-label []
-synonym: "di-Iodination" RELATED Unimod-description []
-synonym: "diiodinationy" EXACT OMSSA-label []
-synonym: "Diiodo" RELATED PSI-MS-label []
-synonym: "I2Tyr" EXACT PSI-MOD-label []
-property_value: DiffAvg "251.79" xsd:float
-property_value: DiffFormula "C 0 H -2 I 2 N 0 O 0" xsd:string
-property_value: DiffMono "251.793295" xsd:float
-property_value: Formula "C 9 H 7 I 2 N 1 O 2" xsd:string
-property_value: MassAvg "414.97" xsd:float
-property_value: MassMono "414.856624" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:130
-is_a: MOD:00501
-is_a: MOD:00998
-
-[Term]
-id: MOD:01141
-name: omega-N-(2,2,5,7,8-pentamethylchroman-6-sulfonyl)-L-arginine
-def: "A protein modification that is produced by reaction with 2,2,5,7,8-pentamethylchroman-6-sulfonyl chloride, Pmc chloride, to form omega-N-(2,2,5,7,8-pentamethylchroman-6-sulfonyl)-L-arginine." [DeltaMass:314]
-comment: From DeltaMass: Average Mass: Formula: C20H30O4N4S1 Monoisotopic Mass Change: 422.199 Average Mass Change: 422.547
-synonym: "PMC arginyl" EXACT DeltaMass-label []
-synonym: "PmcArg" EXACT PSI-MOD-label []
-property_value: DiffAvg "266.36" xsd:float
-property_value: DiffFormula "C 14 H 18 O 3 S 1" xsd:string
-property_value: DiffMono "266.097665" xsd:float
-property_value: Formula "C 20 H 30 N 4 O 4 S 1" xsd:string
-property_value: MassAvg "422.54" xsd:float
-property_value: MassMono "422.198776" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00902
-is_a: MOD:01120
-
-[Term]
-id: MOD:01142
-name: S-15,16-dihydrobiliverdin-L-cysteine
-def: "A protein modification that effectively results from forming an adduct between a cysteine residue and the tetrapyrrole compound 15,16-dihydrobiliverdin." [PubMed:10430868, PubMed:15504407, PubMed:1559975, PubMed:3208761, RESID:AA0428]
-synonym: "(16R)-18-ethenyl-8,12-bis(2-carboxyethyl)-3-[(1R)-1-(((2R)-2-amino-2-carboxy)ethylsulfanyl)ethyl]-2,7,13,17-tetramethyl-15,16-dihydrobilin-1,19(21H,24H)-dione" EXACT RESID-systematic []
-synonym: "15,16-Dhbv" EXACT RESID-alternate []
-synonym: "15,16-dihydrobiliverdin cysteine adduct" EXACT RESID-alternate []
-synonym: "15,16-dihydrobiliverdin IXalpha" EXACT RESID-alternate []
-synonym: "18-ethenyl-8,12-bis(2-carboxyethyl)-3-(2-(cysteinyl-S)-ethyl)-2,7,13,17-tetramethylbiladiene-ab-1,19(16H,21H)-dione" EXACT RESID-alternate []
-synonym: "3'-cysteinyl-15,16-dihydrobiliverdin" EXACT RESID-alternate []
-synonym: "3alpha-cysteinyl-15,16-dihydrobiliverdin" EXACT RESID-alternate []
-synonym: "BINDING 15,16-dihydrobiliverdin (covalent; via 1 link)" EXACT UniProt-feature []
-synonym: "DBV" EXACT RESID-alternate []
-synonym: "S-15,16-dihydrobiliverdin-L-cysteine" EXACT RESID-name []
-property_value: DiffAvg "584.67" xsd:float
-property_value: DiffFormula "C 33 H 36 N 4 O 6 S 0" xsd:string
-property_value: DiffMono "584.263485" xsd:float
-property_value: Formula "C 36 H 41 N 5 O 7 S 1" xsd:string
-property_value: MassAvg "687.81" xsd:float
-property_value: MassMono "687.272670" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00700
-is_a: MOD:00905
-
-[Term]
-id: MOD:01143
-name: 15,16-dihydrobiliverdin-bis-L-cysteine
-def: "A protein modification that effectively results from forming an adduct between two cysteine residues and the tetrapyrrole compound 15,16-dihydrobiliverdin." [PubMed:1559975, PubMed:2222853, PubMed:3208761, PubMed:8420941, RESID:AA0429]
-comment: Cross-link 2.
-synonym: "(16R)-8,12-bis(2-carboxyethyl)-3-[2-(((2R)-2-amino-2-carboxy)ethylsulfanyl)ethyl]-18-[(1Xi)-1-(((2R)-2-amino-2-carboxy)ethylsulfanyl)ethyl]-2,7,13,17-tetramethyl-15,16-dihydrobilin-1,19(21H,24H)-dione" EXACT RESID-systematic []
-synonym: "15,16-Dhbv" EXACT RESID-alternate []
-synonym: "15,16-dihydrobiliverdin cysteine adduct" EXACT RESID-alternate []
-synonym: "15,16-dihydrobiliverdin IXalpha" EXACT RESID-alternate []
-synonym: "15,16-dihydrobiliverdin-bis-L-cysteine" EXACT RESID-name []
-synonym: "3'',18'-biscysteinyl-15,16-dihydrobiliverdin" EXACT RESID-alternate []
-synonym: "3beta,18alpha-biscysteinyl-15,16-dihydrobiliverdin" EXACT RESID-alternate []
-synonym: "8,12-bis(2-carboxyethyl)-3-(2-(cysteinyl-S)-ethyl)-18-(1-(cysteinyl-S)-ethyl)-2,7,13,17-tetramethylbiladiene-ab-1,19(16H,21H)-dione" EXACT RESID-alternate []
-synonym: "BINDING  15,16-dihydrobiliverdin (covalent; via 2 links)" EXACT UniProt-feature []
-synonym: "DBV" EXACT RESID-alternate []
-property_value: DiffAvg "584.67" xsd:float
-property_value: DiffFormula "C 33 H 36 N 4 O 6 S 0" xsd:string
-property_value: DiffMono "584.263485" xsd:float
-property_value: Formula "C 39 H 46 N 6 O 8 S 2" xsd:string
-property_value: MassAvg "790.95" xsd:float
-property_value: MassMono "790.281854" xsd:float
-property_value: Origin "C, C" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00700
-is_a: MOD:02044
-
-[Term]
-id: MOD:01144
-name: S-(sn-1-2,3-dipalmitoylglycerol)-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-(sn-1-2,3-dipalmitoyl-glycerol)cysteine." [DeltaMass:0, PubMed:10896212, PubMed:4575979, PubMed:9056182, RESID:AA0107#var]
-comment: From DeltaMass: Average Mass: 524
-subset: PSI-MOD-slim
-synonym: "S-(sn-1-Dipalmitoyl-glyceryl)- (on Cysteine)" EXACT DeltaMass-label []
-property_value: DiffAvg "550.91" xsd:float
-property_value: DiffFormula "C 35 H 66 N 0 O 4 S 0" xsd:string
-property_value: DiffMono "550.496111" xsd:float
-property_value: Formula "C 38 H 71 N 1 O 5 S 1" xsd:string
-property_value: MassAvg "654.05" xsd:float
-property_value: MassMono "653.505295" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00116
-
-[Term]
-id: MOD:01145
-name: N-tau-(ADP-ribosyl)diphthamide
-def: "A protein modification that effectively converts an L-histidine residue to N-tau-(ADP-ribosyl)diphthamide." [DeltaMass:0, ChEBI:82697]
-comment: From DeltaMass: (name misspelled \"N theta -(ADP-ribosyl) diphthamide (of Histidine)\") Average Mass: 648
-synonym: "MOD_RES ADP-ribosyldiphthamide" EXACT UniProt-feature []
-property_value: DiffAvg "684.51" xsd:float
-property_value: DiffFormula "C 22 H 36 N 7 O 14 P 2" xsd:string
-property_value: DiffMono "684.178999" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 28 H 43 N 10 O 15 P 2" xsd:string
-property_value: MassAvg "821.65" xsd:float
-property_value: MassMono "821.237910" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0672
-is_a: MOD:02087
-is_a: MOD:00909
-relationship: derives_from MOD:00049
-
-[Term]
-id: MOD:01146
-name: S-(6-FAD)-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-(6-FAD)-L-cystine." [DeltaMass:0]
-comment: From DeltaMass: Average Mass: 784 with no citation. This modification has not been reported [JSG].
-subset: PSI-MOD-slim
-synonym: "FAD" RELATED PSI-MS-label []
-synonym: "S6FADCys" EXACT PSI-MOD-label []
-property_value: DiffAvg "783.54" xsd:float
-property_value: DiffFormula "C 27 H 31 N 9 O 15 P 2 S 0" xsd:string
-property_value: DiffMono "783.141485" xsd:float
-property_value: Formula "C 30 H 36 N 10 O 16 P 2 S 1" xsd:string
-property_value: MassAvg "886.68" xsd:float
-property_value: MassMono "886.150669" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "hypothetical" xsd:string
-is_a: MOD:00895
-is_a: MOD:00905
-
-[Term]
-id: MOD:01147
-name: dHex1Hex3HexNAc2 N4-glycosylated asparagine
-def: "modification from DeltaMass" [DeltaMass:0, Unimod:1761]
-comment: From DeltaMass: Average Mass: 1,039
-property_value: DiffAvg "1038.95" xsd:float
-property_value: DiffFormula "C 40 H 66 N 2 O 29" xsd:string
-property_value: DiffMono "1038.375124" xsd:float
-property_value: Formula "C 44 H 72 N 4 O 31" xsd:string
-property_value: MassAvg "1153.06" xsd:float
-property_value: MassMono "1152.418052" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:1761
-xref: GNO:G20956ZV
-is_a: MOD:00725
-is_a: MOD:00160
-
-[Term]
-id: MOD:01148
-name: ubiquitinylated lysine
-def: "A protein modification that effectively crosslinks the N6-amino of a peptidyl lysine with the carboxyl-terminal glycine of a ubiquitin." [PubMed:11125103, PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:02047
-is_a: MOD:02051
-is_a: MOD:01875
-relationship: contains MOD:00134
-
-[Term]
-id: MOD:01149
-name: sumoylated lysine
-def: "A protein modification that effectively crosslinks the N6-amino of a peptidyl lysine with the carboxyl-terminal glycine of a sumo (Small Ubiquitin-related MOdifier) protein." [PubMed:12612601, PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:02047
-is_a: MOD:02051
-is_a: MOD:01875
-relationship: contains MOD:00134
-
-[Term]
-id: MOD:01150
-name: neddylated lysine
-def: "A protein modification that effectively crosslinks the N6-amino of a peptidyl lysine with the carboxyl-terminal glycine of a nedd8 protein." [PubMed:11125103, PubMed:12612601, PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:02051
-is_a: MOD:02047
-is_a: MOD:01875
-relationship: contains MOD:00134
-
-[Term]
-id: MOD:01151
-name: phosphorylated residue with neutral loss of phosphate
-def: "Covalent modification of, or a change resulting in an alteration of the measured molecular mass of, a peptide or protein amino acid phosphorylated residue with a secondary loss of a neutral trihydrogen phosphate molecular fragment." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: DiffAvg "-97.99" xsd:float
-property_value: DiffFormula "C 0 H -3 N 0 O -4 P -1" xsd:string
-property_value: DiffMono "-97.976895" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00432
-
-[Term]
-id: MOD:01152
-name: carboxylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with a carboxylic acid group." [Unimod:299]
-subset: PSI-MOD-slim
-synonym: "Carboxy" RELATED Unimod-interim []
-synonym: "Carboxylation" RELATED Unimod-description []
-property_value: DiffAvg "44.01" xsd:float
-property_value: DiffFormula "C 1 H 0 N 0 O 2" xsd:string
-property_value: DiffMono "43.989829" xsd:float
-property_value: Origin "X" xsd:string
-xref: Unimod:299
-is_a: MOD:01156
-
-[Term]
-id: MOD:01153
-name: methylthiolated residue
-def: "A protein modification that effectively replaces a hydrogen atom with an methylsulfanyl group (thiomethyl group)." [Unimod:39]
-subset: PSI-MOD-slim
-synonym: "Beta-methylthiolation" RELATED Unimod-description []
-synonym: "Methylthio" RELATED Unimod-interim []
-property_value: DiffAvg "46.09" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0 S 1" xsd:string
-property_value: DiffMono "45.987721" xsd:float
-property_value: Origin "X" xsd:string
-xref: Unimod:39
-is_a: MOD:01886
-
-[Term]
-id: MOD:01154
-name: pyruvic acid
-def: "A protein modification that effectively converts a source amino acid to pyruvic acid." [PubMed:10085076, PubMed:3042771, PubMed:8464063, RESID:AA0127]
-subset: PSI-MOD-slim
-synonym: "2-oxopropanoic acid" EXACT RESID-systematic []
-synonym: "MOD_RES Pyruvic acid (Cys)" EXACT UniProt-feature []
-synonym: "MOD_RES Pyruvic acid (Ser)" EXACT UniProt-feature []
-synonym: "pyruvic acid" EXACT RESID-name []
-property_value: Formula "C 3 H 3 O 2" xsd:string
-property_value: MassAvg "71.06" xsd:float
-property_value: MassMono "71.013304" xsd:float
-property_value: Origin "X" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00769
-is_a: MOD:00859
-
-[Term]
-id: MOD:01155
-name: lipoconjugated residue
-def: "A protein modification that effectively results from forming an adduct with a compound containing a lipid-like group either through acylation, alkylation, or amidation." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:01156
-
-[Term]
-id: MOD:01156
-name: protein modification categorized by chemical process
-def: "Modified amino acid residue derived from a natural amino acid by a real or hypothetical chemical process." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:00000
-
-[Term]
-id: MOD:01157
-name: protein modification categorized by amino acid modified
-def: "A protein modification considered either as modified amino acid residues derived from natural amino acids, as a replacement by another natural amino acid, or as a replacement by an unnatural amino acid." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:00000
-
-[Term]
-id: MOD:01158
-name: modified L-selenocysteine residue
-def: "A protein modification that modifies an L-selenocysteine residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: Origin "U" xsd:string
-is_a: MOD:00745
-is_a: MOD:01157
-relationship: derives_from MOD:00031
-
-[Term]
-id: MOD:01159
-name: peptidoglycanated residue
-def: "A protein modification that effectively attaches a residue to murein peptidoglycan by either a pentaglycine linker peptide or a peptide-like L-alanyl-D-glutamyl-2,6-diaminopimelic acid linkage." [PubMed:18688235]
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00764
-
-[Term]
-id: MOD:01160
-name: deaminated residue
-def: "A protein modification that effectively results in the loss of an ammonia, usually by a process of vicinal dehydration, rearrangement, and rehydration with release of ammonia, resulting in a loss of nitrogen with no gain of oxygen." [Unimod:385]
-subset: PSI-MOD-slim
-synonym: "Ammonia-loss" RELATED Unimod-interim []
-synonym: "Loss of ammonia" RELATED Unimod-description []
-property_value: DiffAvg "-17.03" xsd:float
-property_value: DiffFormula "C 0 H -3 N -1 O 0" xsd:string
-property_value: DiffMono "-17.026549" xsd:float
-property_value: Origin "X" xsd:string
-xref: Unimod:385
-is_a: MOD:01156
-
-[Term]
-id: MOD:01161
-name: deoxygenated residue
-def: "A protein modification that effectively removes oxygen atoms from a residue without the removal of hydrogen atoms." [PubMed:14235557, Unimod:447]
-subset: PSI-MOD-slim
-synonym: "Deoxy" RELATED PSI-MS-label []
-synonym: "dOxyRes" EXACT PSI-MOD-label []
-synonym: "reduction" RELATED Unimod-description []
-property_value: DiffAvg "-16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O -1" xsd:string
-property_value: DiffMono "-15.994915" xsd:float
-property_value: Origin "X" xsd:string
-xref: Unimod:447
-is_a: MOD:01472
-
-[Term]
-id: MOD:01162
-name: fucosylated biantennary
-def: "modification from Unimod N-linked glycosylation" [Unimod:308]
-synonym: "dHex(1)Hex(5)HexNAc(4)" RELATED PSI-MS-label []
-synonym: "Fucosylated biantennary" RELATED Unimod-description []
-property_value: DiffAvg "1769.62" xsd:float
-property_value: DiffFormula "C 68 H 112 N 4 O 49" xsd:string
-property_value: DiffMono "1768.639516" xsd:float
-property_value: Formula "C 72 H 118 N 6 O 51" xsd:string
-property_value: MassAvg "1883.73" xsd:float
-property_value: MassMono "1882.682443" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:308
-xref: GNO:G83555HU
-is_a: MOD:00725
-
-[Term]
-id: MOD:01163
-name: guanylated residue
-def: "A protein modification that effectively crosslinks an amino acid residue and 5'-phosphoguanosine through either a phosphodiester or a phosphoramide bond." [DeltaMass:304, Unimod:413]
-comment: From DeltaMass: (formula incorrect, N and O reversed) Average Mass: 345 Formula: C10H12O5N7P1 Monoisotopic Mass Change: 345.047 Average Mass Change: 345.209.
-synonym: "5'phos Guanosyl" EXACT DeltaMass-label []
-synonym: "phospho-guanosine" RELATED Unimod-description []
-synonym: "Phosphoguanosine" RELATED PSI-MS-label []
-property_value: DiffAvg "345.21" xsd:float
-property_value: DiffFormula "C 10 H 12 N 5 O 7 P 1" xsd:string
-property_value: DiffMono "345.047434" xsd:float
-property_value: Origin "X" xsd:string
-xref: Unimod:413
-is_a: MOD:00701
-
-[Term]
-id: MOD:01164
-name: riboflavin-phosphorylated residue
-def: "A protein modification that effectively results from forming an adduct with a compound containing a riboflavin phosphate (flavin mononucleotide, FMN) group through a phosphodiester bond." [Unimod:442]
-subset: PSI-MOD-slim
-synonym: "FMN" RELATED PSI-MS-label []
-synonym: "O3-(riboflavin phosphoryl)" RELATED Unimod-description []
-property_value: DiffAvg "438.33" xsd:float
-property_value: DiffFormula "C 17 H 19 N 4 O 8 P 1" xsd:string
-property_value: DiffMono "438.094050" xsd:float
-property_value: Origin "X" xsd:string
-xref: Unimod:442
-is_a: MOD:00697
-
-[Term]
-id: MOD:01165
-name: adenylated residue
-def: "A protein modification that effectively crosslinks an amino acid residue and 5'-phosphoadenosine through either a phosphodiester or a phosphoramide bond." [DeltaMass:0, Unimod:405]
-comment: From DeltaMass: (name misspelled \"5'phos adenosinyl\") Average Mass: 329
-subset: PSI-MOD-slim
-synonym: "5'phos Adenosinyl" EXACT DeltaMass-label []
-synonym: "AMP binding site" RELATED Unimod-description []
-synonym: "Phosphoadenosine" RELATED PSI-MS-label []
-property_value: DiffAvg "329.21" xsd:float
-property_value: DiffFormula "C 10 H 12 N 5 O 6 P 1" xsd:string
-property_value: DiffMono "329.052520" xsd:float
-property_value: Origin "X" xsd:string
-xref: Unimod:405
-is_a: MOD:00701
-
-[Term]
-id: MOD:01166
-name: uridylated residue
-def: "A protein modification that effectively crosslinks an amino acid residue and 5'-phosphouridine through either a phosphodiester or a phosphoramide bond." [DeltaMass:292, Unimod:417]
-comment: From DeltaMass: (name misspelled \"5'phos Uridinyl\" and formula incorrect, N and O reversed) Average Mass: 306 Formula: C9H11O2N8P1 Monoisotopic Mass Change: 306.025 Average Mass Change: 306.17
-synonym: "5'phos Uridinyl" EXACT DeltaMass-label []
-synonym: "PhosphoUridine" RELATED PSI-MS-label []
-synonym: "uridine phosphodiester" RELATED Unimod-description []
-property_value: DiffAvg "306.17" xsd:float
-property_value: DiffFormula "C 9 H 11 N 2 O 8 P 1" xsd:string
-property_value: DiffMono "306.025302" xsd:float
-property_value: Origin "X" xsd:string
-xref: Unimod:417
-is_a: MOD:00701
-
-[Term]
-id: MOD:01167
-name: molybdopterin guanine dinucleotide
-def: "modification from Unimod" [Unimod:424]
-synonym: "molybdenum bis(molybdopterin guanine dinucleotide)" RELATED Unimod-description []
-synonym: "MolybdopterinGD" RELATED PSI-MS-label []
-property_value: DiffAvg "1572.02" xsd:float
-property_value: DiffFormula "C 40 H 47 Mo 1 N 20 O 26 P 4 S 4" xsd:string
-property_value: DiffMono "1572.985775" xsd:float
-property_value: Origin "X" xsd:string
-xref: Unimod:424
-is_a: MOD:00744
-
-[Term]
-id: MOD:01168
-name: dehydroalanine
-def: "A protein modification that effectively converts a source amino acid residue to dehydroalanine." [PubMed:10220322, PubMed:1547888, PubMed:1815586, PubMed:2914619, PubMed:6838602, PubMed:7947813, PubMed:8239649, RESID:AA0181]
-subset: PSI-MOD-slim
-synonym: "2,3-didehydroalanine" EXACT RESID-alternate []
-synonym: "2-aminoacrylic acid" EXACT RESID-alternate []
-synonym: "2-aminopropenoic acid" EXACT RESID-systematic []
-synonym: "4-methylidene-imidazole-5-one (MIO) active site" EXACT RESID-alternate []
-synonym: "anhydroserine" EXACT RESID-alternate []
-synonym: "dehydroalanine" EXACT RESID-name []
-synonym: "Dha" EXACT RESID-alternate []
-synonym: "dHAla" EXACT PSI-MOD-label []
-synonym: "MOD_RES 2,3-didehydroalanine (Cys)" EXACT UniProt-feature []
-synonym: "MOD_RES 2,3-didehydroalanine (Ser)" EXACT UniProt-feature []
-property_value: Formula "C 3 H 3 N 1 O 1" xsd:string
-property_value: MassAvg "69.06" xsd:float
-property_value: MassMono "69.021464" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00859
-
-[Term]
-id: MOD:01169
-name: L-3-oxoalanine
-def: "A protein modification that effectively converts a source amino acid residue to L-oxoalanine." [DeltaMass:349, PubMed:14563551, PubMed:7628016, PubMed:8681943, PubMed:9478923, RESID:AA0185]
-subset: PSI-MOD-slim
-synonym: "(S)-2-amino-3-oxopropanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-3-oxopropionic acid" EXACT RESID-alternate []
-synonym: "C(alpha)-formylglycine" RELATED RESID-misnomer []
-synonym: "L-3-oxoalanine" EXACT RESID-name []
-synonym: "L-amino-malonic acid semialdehyde" EXACT RESID-alternate []
-synonym: "L-aminomalonaldehydic acid" EXACT RESID-alternate []
-synonym: "L-serinesemialdehyde" RELATED RESID-misnomer []
-synonym: "MOD_RES 3-oxoalanine (Cys)" EXACT UniProt-feature []
-synonym: "MOD_RES 3-oxoalanine (Ser)" EXACT UniProt-feature []
-property_value: Formula "C 3 H 3 N 1 O 2" xsd:string
-property_value: MassAvg "85.06" xsd:float
-property_value: MassMono "85.016378" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00859
-
-[Term]
-id: MOD:01170
-name: pyruvic acid iminylated residue
-def: "A protein modification that effectively forms a 2-ketoimine of pyruvicacid with a residue amino group." [Unimod:422]
-synonym: "N-pyruvic acid 2-iminyl" RELATED Unimod-description []
-synonym: "PyruvicAcidIminyl" RELATED PSI-MS-label []
-property_value: DiffAvg "70.05" xsd:float
-property_value: DiffFormula "C 3 H 2 N 0 O 2" xsd:string
-property_value: DiffMono "70.005479" xsd:float
-property_value: Origin "X" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:422
-is_a: MOD:01156
-
-[Term]
-id: MOD:01171
-name: O-acetyl-L-threonine
-def: "A protein modification that effectively converts an L-threonine residue to O-acetyl-L-threonine." [PubMed:16728640, RESID:AA0423, Unimod:1#T]
-subset: PSI-MOD-slim
-synonym: "(2S,3R)-3-(acetyloxy)-2-aminobutanoic acid" EXACT RESID-systematic []
-synonym: "Acetylation" RELATED Unimod-description []
-synonym: "ACT_SITE O-acetylthreonine intermediate" EXACT UniProt-feature []
-synonym: "MOD_RES O-acetylthreonine" EXACT UniProt-feature []
-synonym: "O-acetyl-L-threonine" EXACT RESID-name []
-synonym: "O-acetylthreonine" EXACT RESID-alternate []
-synonym: "OAcThr" EXACT PSI-MOD-label []
-synonym: "threonine acetate ester" EXACT RESID-alternate []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 2 H 2 N 0 O 1" xsd:string
-property_value: DiffMono "42.010565" xsd:float
-property_value: Formula "C 6 H 9 N 1 O 3" xsd:string
-property_value: MassAvg "143.14" xsd:float
-property_value: MassMono "143.058243" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:1
-xref: uniprot.ptm:PTM-0233
-is_a: MOD:00644
-is_a: MOD:01186
-
-[Term]
-id: MOD:01172
-name: N-alanyl-glycosylsphingolipidinositolethanolamine
-def: "A protein modification that effectively converts an L-alanine residue to N-alanyl-glycosylsphingolipidinositolethanolamine." [PubMed:12626404, RESID:AA0424]
-synonym: "GSIAla" EXACT PSI-MOD-label []
-synonym: "LIPID GPI-like-anchor amidated alanine" EXACT UniProt-feature []
-synonym: "N-alanyl-glycosylsphingolipidinositolethanolamine" EXACT RESID-name []
-property_value: DiffAvg "123.05" xsd:float
-property_value: DiffFormula "C 2 H 6 N 1 O 3 P 1" xsd:string
-property_value: DiffMono "123.008530" xsd:float
-property_value: Formula "C 5 H 12 N 2 O 5 P 1" xsd:string
-property_value: MassAvg "211.13" xsd:float
-property_value: MassMono "211.048383" xsd:float
-property_value: Origin "A" xsd:string
-property_value: Source "hypothetical" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0144
-is_a: MOD:00466
-is_a: MOD:00901
-
-[Term]
-id: MOD:01173
-name: N-asparaginyl-glycosylsphingolipidinositolethanolamine
-def: "A protein modification that effectively converts an L-asparagine residue to N-asparaginyl-glycosylsphingolipidinositolethanolamine." [PubMed:12626404, RESID:AA0425]
-synonym: "GSIAsn" EXACT PSI-MOD-label []
-synonym: "LIPID GPI-like-anchor amidated asparagine" EXACT UniProt-feature []
-synonym: "N-asparaginyl-glycosylsphingolipidinositolethanolamine" EXACT RESID-name []
-property_value: DiffAvg "123.05" xsd:float
-property_value: DiffFormula "C 2 H 6 N 1 O 3 P 1" xsd:string
-property_value: DiffMono "123.008530" xsd:float
-property_value: Formula "C 6 H 13 N 3 O 6 P 1" xsd:string
-property_value: MassAvg "254.16" xsd:float
-property_value: MassMono "254.054197" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "hypothetical" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0145
-is_a: MOD:00466
-is_a: MOD:00903
-
-[Term]
-id: MOD:01174
-name: S-(15-deoxy-Delta12,14-prostaglandin J2-9-yl)-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-(15-deoxy-Delta12,14-prostaglandin J2-9-yl)-L-cysteine." [ChEBI:27485, PubMed:11466314, PubMed:12684535, RESID:AA0426]
-synonym: "(2R)-2-amino-3-([(5Z,9Xi,12E,14Z)-1-hydroxy-1,11-oxoprosta-5,12,14-trien-9-yl]sulfanyl)propanoic acid" EXACT RESID-alternate []
-synonym: "(5Z,9Xi,12E,14Z)-9-([(2R)-2-amino-3-carboxyethyl]sulfanyl)-11-oxoprosta-5,12,14-trien-1-oic acid" EXACT RESID-systematic []
-synonym: "LIPID S-(15-deoxy-Delta12,14-prostaglandin J2-9-yl)cysteine" EXACT UniProt-feature []
-synonym: "PG-J2Cys" EXACT PSI-MOD-label []
-synonym: "S-(15-deoxy-Delta12,14-prostaglandin J2-9-yl)-L-cysteine" EXACT RESID-name []
-property_value: DiffAvg "316.44" xsd:float
-property_value: DiffFormula "C 20 H 28 N 0 O 3 S 0" xsd:string
-property_value: DiffMono "316.203845" xsd:float
-property_value: Formula "C 23 H 33 N 1 O 4 S 1" xsd:string
-property_value: MassAvg "419.58" xsd:float
-property_value: MassMono "419.213030" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0447
-is_a: MOD:00905
-is_a: MOD:01155
-
-[Term]
-id: MOD:01175
-name: S-phycourobilin-L-cysteine
-def: "A protein modification that effectively results from forming an adduct between a cysteine residue and the tetrapyrrole compound phycourobilin." [PubMed:1903388, PubMed:3208761, PubMed:3838747, RESID:AA0427]
-synonym: "(2S,3R,16R)-18-ethenyl-3-[(1R)-1-([(R)-2-amino-2-carboxyethyl]sulfanyl)ethyl]-8,12-bis(2-carboxyethyl)-2,7,13,17-tetramethyl-4,5,15,16-tetrahydrobiline-1,19(21H,22H,24H)-dione" EXACT RESID-systematic []
-synonym: "18-ethenyl-3-[1-(2-amino-2-carboxyethylsulfanyl)ethyl]-2,3,15,16-dihydro-2,7,13,17-tetramethyl-1,19-dioxo-(21H,22H,24H)-bilin-8,12-dipropanoic acid" EXACT RESID-alternate []
-synonym: "BINDING Phycourobilin chromophore (covalent; via 1 link)" EXACT UniProt-feature []
-synonym: "phycourobilin cysteine adduct" EXACT RESID-alternate []
-synonym: "PUB" EXACT RESID-alternate []
-synonym: "PUBCys" EXACT PSI-MOD-label []
-synonym: "S-phycourobilin-L-cysteine" EXACT RESID-name []
-property_value: DiffAvg "586.69" xsd:float
-property_value: DiffFormula "C 33 H 38 N 4 O 6 S 0" xsd:string
-property_value: DiffMono "586.279135" xsd:float
-property_value: Formula "C 36 H 43 N 5 O 7 S 1" xsd:string
-property_value: MassAvg "689.83" xsd:float
-property_value: MassMono "689.288320" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00700
-is_a: MOD:00905
-
-[Term]
-id: MOD:01176
-name: L-dehydrolysinonorleucine
-def: "A protein modification that effectively cross-links an L-lysine residue and an L-lysine residue converted to allysine with a carbon-nitrogen bond to form L-dehydrolysinonorleucine." [PubMed:16929109, RESID:AA0430]
-comment: Cross-link 2.
-synonym: "(2S)-2-amino-6-([(5S)-5-amino-5-carboxypentylidene]amino)hexanoic acid" EXACT RESID-systematic []
-synonym: "6-(N6-L-didehydrolysino)-L-norleucine" EXACT RESID-alternate []
-synonym: "CROSSLNK Dehydrolysinonorleucine (Lys-Lys)" EXACT UniProt-feature []
-synonym: "dehydrolysinorleucine [misspelling]" EXACT RESID-alternate []
-synonym: "dehydrolysylnorleucine" EXACT RESID-alternate []
-synonym: "didehydrolysinonorleucine" EXACT RESID-alternate []
-synonym: "L-dehydrolysinonorleucine" EXACT RESID-name []
-synonym: "N6-[(5S)-5-amino-5-carboxypentylidene]-L-lysine" EXACT RESID-alternate []
-synonym: "XLNK6NleN6Lys" EXACT PSI-MOD-label []
-property_value: DiffAvg "-19.05" xsd:float
-property_value: DiffFormula "C 0 H -5 N -1 O 0" xsd:string
-property_value: DiffMono "-19.042199" xsd:float
-property_value: Formula "C 12 H 19 N 3 O 2" xsd:string
-property_value: MassAvg "237.30" xsd:float
-property_value: MassMono "237.147727" xsd:float
-property_value: Origin "K, K" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00692
-is_a: MOD:02051
-
-[Term]
-id: MOD:01177
-name: 1'-(1,2,3-trihydroxyprop-2-yl)-L-histidine
-def: "A protein modification that effectively converts an L-histidine residue to 1'-(1,2,3-trihydroxyprop-2-yl)-L-histidine." [PubMed:16760471, RESID:AA0431]
-synonym: "(S)-2-amino-3-[1-(1,2,3-trihydroxypropan-2-yl)-1H-imidazol-4-yl]propanoic acid" EXACT RESID-systematic []
-synonym: "1'-(1,2,3-trihydroxyprop-2-yl)-L-histidine" EXACT RESID-name []
-synonym: "1-[1,2-dihydroxy-1-(hydroxymethyl)ethyl]-L-histidine" EXACT RESID-alternate []
-synonym: "MOD_RES Tele-(1,2,3-trihydroxypropan-2-yl)histidine" EXACT UniProt-feature []
-synonym: "N(epsilon)-histidine dihydroxyacetone adduct" EXACT RESID-alternate []
-synonym: "N(tau)-(1,2,3-trihydroxypropan-2-yl)histidine" EXACT RESID-alternate []
-synonym: "NtauDHAHis" EXACT PSI-MOD-label []
-synonym: "tele-(1,2,3-trihydroxypropan-2-yl)histidine" EXACT RESID-alternate []
-property_value: DiffAvg "90.08" xsd:float
-property_value: DiffFormula "C 3 H 6 N 0 O 3" xsd:string
-property_value: DiffMono "90.031694" xsd:float
-property_value: Formula "C 9 H 13 N 3 O 4" xsd:string
-property_value: MassAvg "227.22" xsd:float
-property_value: MassMono "227.090606" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0416
-is_a: MOD:00909
-
-[Term]
-id: MOD:01178
-name: S-(aspart-4-yloxy) thiocarbonate
-def: "A protein modification that effectively converts an L-aspartic acid residue to S-(aspart-4-yloxy) thiocarbonate." [PubMed:16627948, RESID:AA0432]
-comment: This modification was originally observed in an Entamoeba histolytica enzyme expressed in Escherichia coli. It was not chemically confirmed or characterized. It did not appear in a later model at higher resolution by the same group. This is a deprecated entry in RESID. It probably does not occur naturally [JSG].
-synonym: "(2S)-2-amino-4-(carboxysulfanyl)oxy-4-oxobutanoic acid" EXACT RESID-systematic []
-synonym: "4-aspartyloxysulfanylcarbonate" EXACT RESID-alternate []
-synonym: "AspOSCO2H" EXACT PSI-MOD-label []
-synonym: "O-carboxysulfanyl-4-oxo-L-homoserine" EXACT RESID-alternate []
-synonym: "S-(aspart-4-yloxy) thiocarbonate" EXACT RESID-name []
-property_value: DiffAvg "76.07" xsd:float
-property_value: DiffFormula "C 1 H 0 N 0 O 2 S 1" xsd:string
-property_value: DiffMono "75.961900" xsd:float
-property_value: Formula "C 5 H 5 N 1 O 5 S 1" xsd:string
-property_value: MassAvg "191.16" xsd:float
-property_value: MassMono "190.988843" xsd:float
-property_value: Origin "D" xsd:string
-property_value: Source "hypothetical" xsd:string
-is_a: MOD:00904
-
-[Term]
-id: MOD:01179
-name: N,N-dimethyl-L-alanine
-def: "A protein modification that effectively converts an L-alanine residue to N,N-dimethyl-L-alanine." [PubMed:17691833, PubMed:387091, RESID:AA0433]
-synonym: "(S)-1-carboxy-N,N-dimethylaminoethane" EXACT RESID-alternate []
-synonym: "(S)-2-(dimethylamino)propanoic acid" EXACT RESID-systematic []
-synonym: "MOD_RES N,N-dimethylalanine" EXACT UniProt-feature []
-synonym: "N,N-dimethyl-L-alanine" EXACT RESID-name []
-synonym: "N,N-dimethylalanine" EXACT RESID-alternate []
-synonym: "NMe2Ala" EXACT PSI-MOD-label []
-property_value: DiffAvg "28.05" xsd:float
-property_value: DiffFormula "C 2 H 4 N 0 O 0" xsd:string
-property_value: DiffMono "28.031300" xsd:float
-property_value: Formula "C 5 H 10 N 1 O 1" xsd:string
-property_value: MassAvg "100.14" xsd:float
-property_value: MassMono "100.076239" xsd:float
-property_value: Origin "A" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0178
-is_a: MOD:01461
-is_a: MOD:01686
-
-[Term]
-id: MOD:01180
-name: 2-hydroxyglycine observational artifact
-def: "A protein modification that effectively converts a glycine residue to 2-hydroxyglycine." [ChEBI:38048, PubMed:16178056, PubMed:17431180, PubMed:17823333, RESID:AA0434]
-comment: CAUTION - peptides of 2-hydroxyglycine are known to be unstable, decaying to break the peptide backbone or to form peptidyl amides [see J. Am. Chem. Soc. 111, 1933-1934, 1989, and J. Org. Chem. 57, 3916-3921, 1992]. If computer analysis of tandem mass-spectrometric results predicts this modification, then it is most probable that there are multiple isobaric peptides differing in the location of multiple hydroxylation modifications [JSG].
-synonym: "2-hydroxyglycine" EXACT RESID-name []
-synonym: "2HyGly" EXACT PSI-MOD-label []
-synonym: "alpha-hydroxyglycine" EXACT RESID-alternate []
-synonym: "amino(hydroxy)acetic acid" EXACT RESID-systematic []
-synonym: "aminohydroxyacetic acid" EXACT RESID-alternate []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 2 H 3 N 1 O 2" xsd:string
-property_value: MassAvg "73.05" xsd:float
-property_value: MassMono "73.016378" xsd:float
-property_value: Origin "G" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00425
-is_a: MOD:00908
-
-[Term]
-id: MOD:01181
-name: L-aspartic acid 4-methyl ester
-def: "A protein modification that effectively converts an L-aspartic acid residue to L-aspartate 4-methyl ester." [OMSSA:69, PubMed:1556110, PubMed:16888766, PubMed:9629898, RESID:AA0435, Unimod:34#D]
-comment: CAUTION - observations of this modifation are attributable to artifacts produced in preparation. It is extremely unlikely that eukaryotes produce this modification, because an enzyme acting to form the methyl ester of L-aspartyl peptides would interfere with the D-aspartyl peptide repair mechanism [JSG].
-synonym: "(2S)-2-amino-4-methoxy-4-oxobutanoic acid" EXACT RESID-systematic []
-synonym: "2-aminobutanedioic acid 4-methyl ester" EXACT RESID-alternate []
-synonym: "4-methyl L-2-aminosuccinic acid" EXACT RESID-alternate []
-synonym: "4-methyl L-aspartate" EXACT RESID-alternate []
-synonym: "4-methyl L-hydrogen aspartate" EXACT RESID-alternate []
-synonym: "aspartic acid 4-methyl ester" EXACT RESID-alternate []
-synonym: "aspartic acid beta-methyl ester" EXACT RESID-alternate []
-synonym: "L-aspartic acid 4-methyl ester" EXACT RESID-name []
-synonym: "meesterd" EXACT OMSSA-label []
-synonym: "Methyl" RELATED PSI-MS-label []
-synonym: "O4MeAsp" EXACT PSI-MOD-label []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 5 H 7 N 1 O 3" xsd:string
-property_value: MassAvg "129.12" xsd:float
-property_value: MassMono "129.042593" xsd:float
-property_value: Origin "D" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:34
-is_a: MOD:00393
-is_a: MOD:01681
-
-[Term]
-id: MOD:01182
-name: 6-(S-L-cysteinyl)-8alpha-(-3'-L-histidino)-FAD
-def: "A protein modification that crosslinks a cysteine and a histidine residue by forming the adduct 6-(S-L-cysteinyl)-8alpha-(-3'-L-histidino)-FAD." [PubMed:, RESID:AA0436]
-comment: Cross-link 2.
-subset: PSI-MOD-slim
-synonym: "6-((R)-2-amino-2-carboxyethyl)sulfanyl-8alpha-[4-((S)-2-amino-2-carboxyethyl)imidazol-3-yl]-riboflavin 5'-(trihydrogen diphosphate) 5'->5'-ester with adenosine" EXACT RESID-systematic []
-synonym: "6-(S-cysteinyl)-8alpha-(N(delta1)-histidyl)-FAD" EXACT RESID-alternate []
-synonym: "6-(S-cysteinyl)-8alpha-(N(pi)-histidyl)-FAD" EXACT RESID-alternate []
-synonym: "6-(S-cysteinyl)-8alpha-(N3'-histidyl)-FAD" EXACT RESID-alternate []
-synonym: "6-(S-cysteinyl)-8alpha-(pros-histidyl)-FAD" EXACT RESID-alternate []
-synonym: "6-(S-L-cysteinyl)-8alpha-(N3'-L-histidino)-FAD" EXACT RESID-name []
-synonym: "BINDING FAD (covalent; via 2 links)" EXACT UniProt-feature []
-synonym: "BINDING FAD (covalent; via 2 links, pros nitrogen)" EXACT UniProt-feature []
-synonym: "CROSSLNK 6-(S-cysteinyl)-8alpha-(pros-histidyl)-FAD (His-Cys)" EXACT UniProt-feature []
-synonym: "SCys6-NprosHis8a-FAD" EXACT PSI-MOD-label []
-property_value: DiffAvg "781.52" xsd:float
-property_value: DiffFormula "C 27 H 29 N 9 O 15 P 2 S 0" xsd:string
-property_value: DiffMono "781.125835" xsd:float
-property_value: Formula "C 36 H 41 N 13 O 17 P 2 S 1" xsd:string
-property_value: MassAvg "1021.81" xsd:float
-property_value: MassMono "1021.193931" xsd:float
-property_value: Origin "C, H" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0681
-is_a: MOD:02044
-is_a: MOD:02048
-is_a: MOD:01621
-
-[Term]
-id: MOD:01183
-name: L-selenocystine (oxidized selenocysteine) (Sec-Sec)
-def: "A protein modification that effectively cross-links two L-selenocysteine residues to form L-selenocystine," [ChEBI:28553, PubMed:17715293, PubMed:6076213, RESID:AA0437]
-comment: Cross-link 2; for formation of the same modification by substitution of 2 selenium for 2 sulfur atoms in L-cystine, see MOD:01184.
-subset: PSI-MOD-slim
-synonym: "(R,R)-3,3'-diselane-1,2-diylbis(2-aminopropanoic acid)" EXACT RESID-systematic []
-synonym: "3,3'-diselenobis(2-aminopropanoic acid)" EXACT RESID-alternate []
-synonym: "3,3'-diselenobisalanine" EXACT RESID-alternate []
-synonym: "3,3'-diselenodialanine" EXACT RESID-alternate []
-synonym: "beta,beta'-diamino-beta,beta'-dicarboxydiethyldiselenide" EXACT RESID-alternate []
-synonym: "beta,beta'-diselenodialanine" EXACT RESID-alternate []
-synonym: "bis(alpha-aminopropionic acid)-beta-diselenide" EXACT RESID-alternate []
-synonym: "bis(beta-amino-beta-carboxyethyl)diselenide" EXACT RESID-alternate []
-synonym: "CROSSLNK Selenocystine (Sec-Sec)" EXACT UniProt-feature []
-synonym: "diselenocysteine" EXACT RESID-alternate []
-synonym: "L-selenocystine" EXACT RESID-name []
-synonym: "Sec2" EXACT PSI-MOD-label []
-synonym: "selenium cystine" EXACT RESID-alternate []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0 Se 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 6 H 8 N 2 O 2 Se 2" xsd:string
-property_value: MassAvg "298.08" xsd:float
-property_value: MassMono "299.891620" xsd:float
-property_value: Origin "U, U" xsd:string
-property_value: Source "hypothetical" xsd:string
-is_a: MOD:00692
-is_a: MOD:01158
-
-[Term]
-id: MOD:01184
-name: L-selenocystine (selenium disubstituted L-cystine)
-def: "A protein modification that effectively substitutes two selenium atoms for two sulfur atoms in L-cystine to form L-selenocystine." [PubMed:17715293, RESID:AA0437#CYS2]
-comment: Cross-link 2; for formation of the same modification by oxidation of two L-selenocysteine residues, see MOD:01183.
-synonym: "(R,R)-3,3'-diselane-1,2-diylbis(2-aminopropanoic acid)" EXACT RESID-systematic []
-synonym: "3,3'-diselenobis(2-aminopropanoic acid)" EXACT RESID-alternate []
-synonym: "3,3'-diselenobisalanine" EXACT RESID-alternate []
-synonym: "3,3'-diselenodialanine" EXACT RESID-alternate []
-synonym: "beta,beta'-diamino-beta,beta'-dicarboxydiethyldiselenide" EXACT RESID-alternate []
-synonym: "beta,beta'-diselenodialanine" EXACT RESID-alternate []
-synonym: "bis(alpha-aminopropionic acid)-beta-diselenide" EXACT RESID-alternate []
-synonym: "bis(beta-amino-beta-carboxyethyl)diselenide" EXACT RESID-alternate []
-synonym: "CROSSLNK Selenocystine (Sec-Sec)" EXACT UniProt-feature []
-synonym: "diselenocysteine" EXACT RESID-alternate []
-synonym: "L-selenocystine" EXACT RESID-name []
-synonym: "Se2(S2)Cys2" EXACT PSI-MOD-label []
-synonym: "selenium cystine" EXACT RESID-alternate []
-property_value: DiffAvg "91.81" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0 S -2 Se 2" xsd:string
-property_value: DiffMono "93.873250" xsd:float
-property_value: Formula "C 6 H 8 N 2 O 2 Se 2" xsd:string
-property_value: MassAvg "298.08" xsd:float
-property_value: MassMono "299.891620" xsd:float
-property_value: Origin "C, C" xsd:string
-property_value: Source "hypothetical" xsd:string
-is_a: MOD:00905
-
-[Term]
-id: MOD:01185
-name: 4-amidated L-aspartic acid
-def: "A protein modification that effectively converts an L-aspartic acid residue to L-asparagine." [PubMed:17962566, RESID:AA0003#ASP]
-synonym: "(2S)-2-amino-4-butanediamic acid" EXACT RESID-systematic []
-synonym: "2,4-bis(azanyl)-4-oxobutanoic acid" EXACT RESID-alternate []
-synonym: "2,4-diamino-4-oxobutanoic acid" EXACT RESID-alternate []
-synonym: "2-amino-3-carbamoylpropanoic acid" EXACT RESID-alternate []
-synonym: "2-amino-4-butanediamic acid" EXACT RESID-alternate []
-synonym: "2-aminosuccinamic acid" EXACT RESID-alternate []
-synonym: "2-aminosuccinic acid 4-amide" EXACT RESID-alternate []
-synonym: "4NAsp" EXACT PSI-MOD-label []
-synonym: "alpha-amino-beta-carbamylpropionic acid" EXACT RESID-alternate []
-synonym: "alpha-aminosuccinamic acid" EXACT RESID-alternate []
-synonym: "aspartic acid 4-amide" EXACT RESID-alternate []
-synonym: "aspartic acid beta-amide" EXACT RESID-alternate []
-synonym: "beta-asparagine" EXACT RESID-alternate []
-synonym: "L-asparagine" EXACT RESID-name []
-synonym: "MOD_RES Amidated aspartic acid" EXACT UniProt-feature []
-property_value: DiffAvg "-0.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 1 O -1" xsd:string
-property_value: DiffMono "-0.984016" xsd:float
-property_value: Formula "C 4 H 6 N 2 O 2" xsd:string
-property_value: MassAvg "114.10" xsd:float
-property_value: MassMono "114.042927" xsd:float
-property_value: Origin "D" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00674
-is_a: MOD:00904
-
-[Term]
-id: MOD:01186
-name: monoacetylated L-threonine
-def: "A protein modification that effectively converts an L-threonine residue to either N-acetyl-L-threonne, or O-acetyl-Lthreonine." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "AcThr" EXACT PSI-MOD-label []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 2 H 2 N 0 O 1" xsd:string
-property_value: DiffMono "42.010565" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00394
-is_a: MOD:00917
-
-[Term]
-id: MOD:01187
-name: L-pyrrolysine residue
-def: "A protein modification that inserts or replaces a residue with an L-pyrrolysine residue, a natural pretranslational modification." [ChEBI:21860, PubMed:11435424, PubMed:12029131, PubMed:12029132, PubMed:15314242, PubMed:16096277, RESID:AA0321, Unimod:435]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-6-[(2R,3R)-3-methyl-3,4-dihydro-2H-pyrrol-2-ylcarbonyl]aminohexanoic acid" EXACT RESID-systematic []
-synonym: "2-azanyl-6-[(2R,3R)-3-methyl-3,4-dihydro-2H-pyrrol-2-ylcarbonyl]azanylhexanoic acid" EXACT RESID-alternate []
-synonym: "L-pyrrolysine" EXACT RESID-name []
-synonym: "monomethylamine methyltransferase cofactor lysine adduct" EXACT RESID-alternate []
-synonym: "N6-(4-methyl-1,2-didehydropyrrolidine-5-carboxyl)-L-lysine" EXACT RESID-alternate []
-synonym: "N6-(4-methyl-delta-1-pyrroline-5-carboxyl)-L-lysine" EXACT RESID-alternate []
-synonym: "N6-([(2R,3R)-3-methyl-3,4-dihydro-2H-pyrrol-2-yl]carbonyl)-L-lysine" EXACT RESID-alternate []
-synonym: "NON_STD Pyrrolysine" EXACT UniProt-feature []
-synonym: "Pyl" EXACT PSI-MOD-label []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 12 H 19 N 3 O 2" xsd:string
-property_value: MassAvg "237.30" xsd:float
-property_value: MassMono "237.147727" xsd:float
-property_value: Origin "O" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:435
-is_a: MOD:00868
-
-[Term]
-id: MOD:01188
-name: N-ethyl iodoacetamide-d5 - site Y
-def: "modification from Unimod Isotopic label -" [PubMed:11710128, PubMed:12766232, PubMed:3155470, PubMed:957432, Unimod:212#Y]
-synonym: "N-ethyl iodoacetamide-d5" RELATED Unimod-description []
-synonym: "NEIAA:2H(5)" RELATED PSI-MS-label []
-property_value: DiffAvg "90.08" xsd:float
-property_value: DiffFormula "C 4 (1)H 2 (2)H 5 N 1 O 1" xsd:string
-property_value: DiffMono "90.084148" xsd:float
-property_value: Formula "C 13 (1)H 11 (2)H 5 N 2 O 3" xsd:string
-property_value: MassAvg "253.15" xsd:float
-property_value: MassMono "253.147476" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:212
-is_a: MOD:00562
-
-[Term]
-id: MOD:01189
-name: N-ethyl iodoacetamide-d5 - site C
-def: "modification from Unimod Isotopic label -" [PubMed:12766232, Unimod:212#C]
-synonym: "N-ethyl iodoacetamide-d5" RELATED Unimod-description []
-synonym: "NEIAA:2H(5)" RELATED PSI-MS-label []
-property_value: DiffAvg "90.08" xsd:float
-property_value: DiffFormula "C 4 (1)H 2 (2)H 5 N 1 O 1" xsd:string
-property_value: DiffMono "90.084148" xsd:float
-property_value: Formula "C 7 (1)H 7 (2)H 5 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "193.09" xsd:float
-property_value: MassMono "193.093332" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:212
-is_a: MOD:00562
-
-[Term]
-id: MOD:01190
-name: dibromo
-def: "Modification from Unimod Chemical derivative. OBSOLETE because duplicate and redundant with MOD:01006. Remap to MOD:01006." [Unimod:534]
-synonym: "Dibromo" RELATED PSI-MS-label []
-synonym: "Dibromo" RELATED Unimod-description []
-property_value: DiffAvg "157.79" xsd:float
-property_value: DiffFormula "Br 2 H -2" xsd:string
-property_value: DiffMono "155.821024" xsd:float
-property_value: Origin "Y" xsd:string
-replaced_by: MOD:01006
-xref: Unimod:534
-is_obsolete: true
-
-[Term]
-id: MOD:01191
-name: N-ethyl iodoacetamide-d0 - site C
-def: "modification from Unimod Isotopic label -" [PubMed:12766232, Unimod:211#C]
-synonym: "N-ethyl iodoacetamide-d0" RELATED Unimod-description []
-synonym: "NEIAA" RELATED PSI-MS-label []
-property_value: DiffAvg "85.11" xsd:float
-property_value: DiffFormula "C 4 H 7 N 1 O 1" xsd:string
-property_value: DiffMono "85.052764" xsd:float
-property_value: Formula "C 7 H 12 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "188.25" xsd:float
-property_value: MassMono "188.061949" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:211
-is_a: MOD:00561
-
-[Term]
-id: MOD:01192
-name: N-ethyl iodoacetamide-d0 - site Y
-def: "modification from Unimod Isotopic label -" [PubMed:11760118, PubMed:12766232, Unimod:211#Y]
-synonym: "N-ethyl iodoacetamide-d0" RELATED Unimod-description []
-synonym: "NEIAA" RELATED PSI-MS-label []
-property_value: DiffAvg "85.11" xsd:float
-property_value: DiffFormula "C 4 H 7 N 1 O 1" xsd:string
-property_value: DiffMono "85.052764" xsd:float
-property_value: Formula "C 13 H 16 N 2 O 3" xsd:string
-property_value: MassAvg "248.28" xsd:float
-property_value: MassMono "248.116092" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:211
-is_a: MOD:00561
-
-[Term]
-id: MOD:01193
-name: pyridyl thiol modified L-threonine
-def: "modification from Unimod Chemical derivative -" [PubMed:1093385, Unimod:264#T]
-synonym: "PET" RELATED PSI-MS-label []
-synonym: "phosphorylation to pyridyl thiol" RELATED Unimod-description []
-property_value: DiffAvg "121.20" xsd:float
-property_value: DiffFormula "C 7 H 7 N 1 O -1 S 1" xsd:string
-property_value: DiffMono "121.035006" xsd:float
-property_value: Formula "C 11 H 14 N 2 O 1 S 1" xsd:string
-property_value: MassAvg "222.31" xsd:float
-property_value: MassMono "222.082684" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:264
-is_a: MOD:00917
-is_a: MOD:00586
-
-[Term]
-id: MOD:01194
-name: pyridyl thiol modified L-serine
-def: "modification from Unimod Chemical derivative -" [PubMed:15279557, Unimod:264#S]
-synonym: "PET" RELATED PSI-MS-label []
-synonym: "phosphorylation to pyridyl thiol" RELATED Unimod-description []
-property_value: DiffAvg "121.20" xsd:float
-property_value: DiffFormula "C 7 H 7 N 1 O -1 S 1" xsd:string
-property_value: DiffMono "121.035006" xsd:float
-property_value: Formula "C 10 H 12 N 2 O 1 S 1" xsd:string
-property_value: MassAvg "208.28" xsd:float
-property_value: MassMono "208.067034" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:264
-is_a: MOD:00916
-is_a: MOD:00586
-
-[Term]
-id: MOD:01195
-name: benzoyl labeling reagent light form - site K
-def: "modification from Unimod Isotopic label -" [PubMed:11813307, PubMed:12777388, PubMed:15456300, Unimod:136#K]
-synonym: "Benzoyl" RELATED PSI-MS-label []
-synonym: "labeling reagent light form (N-term & K)" RELATED Unimod-description []
-property_value: DiffAvg "104.11" xsd:float
-property_value: DiffFormula "C 7 H 4 O 1" xsd:string
-property_value: DiffMono "104.026215" xsd:float
-property_value: Formula "C 13 H 16 N 2 O 2" xsd:string
-property_value: MassAvg "232.28" xsd:float
-property_value: MassMono "232.121178" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:136
-is_a: MOD:00505
-
-[Term]
-id: MOD:01196
-name: 5-dimethylaminonaphthalene-1-sulfonyl - site K
-def: "OBSOLETE because redundant, replaced with MOD:01654. Remap to MOD:01654." [Unimod:139]
-synonym: "5-dimethylaminonaphthalene-1-sulfonyl" RELATED Unimod-description []
-synonym: "Dansyl" RELATED PSI-MS-label []
-property_value: DiffAvg "233.29" xsd:float
-property_value: DiffFormula "C 12 H 11 N 1 O 2 S 1" xsd:string
-property_value: DiffMono "233.051050" xsd:float
-property_value: Formula "C 18 H 23 N 3 O 3 S 1" xsd:string
-property_value: MassAvg "361.46" xsd:float
-property_value: MassMono "361.146013" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-replaced_by: MOD:01654
-xref: Unimod:139
-is_obsolete: true
-
-[Term]
-id: MOD:01197
-name: N-heptosyl-L-glutamine
-def: "A protein modification that effectively converts an L-glutamine residue to N-heptosyl-L-glutamine." [Unimod:490#Q]
-comment: From Unimod with no citation [JSG].
-synonym: "Hep" RELATED PSI-MS-label []
-synonym: "Heptose" RELATED Unimod-description []
-property_value: DiffAvg "192.17" xsd:float
-property_value: DiffFormula "C 7 H 12 O 6" xsd:string
-property_value: DiffMono "192.063388" xsd:float
-property_value: Formula "C 12 H 20 N 2 O 8" xsd:string
-property_value: MassAvg "320.30" xsd:float
-property_value: MassMono "320.121966" xsd:float
-property_value: Origin "Q" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:490
-is_a: MOD:00925
-
-[Term]
-id: MOD:01198
-name: O-heptosyl-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O-heptosyl-L-serine." [Unimod:490#S]
-comment: From Unimod with no citation [JSG].
-synonym: "Hep" RELATED PSI-MS-label []
-synonym: "Heptose" RELATED Unimod-description []
-property_value: DiffAvg "192.17" xsd:float
-property_value: DiffFormula "C 7 H 12 O 6" xsd:string
-property_value: DiffMono "192.063388" xsd:float
-property_value: Formula "C 10 H 17 N 1 O 8" xsd:string
-property_value: MassAvg "279.25" xsd:float
-property_value: MassMono "279.095417" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:490
-is_a: MOD:00925
-
-[Term]
-id: MOD:01199
-name: N-heptosyl-L-arginine
-def: "A protein modification that effectively converts an L-arginine residue to an N-heptosyl-L-arginine." [Unimod:490#R]
-comment: From Unimod with no citation [JSG].
-synonym: "Hep" RELATED PSI-MS-label []
-synonym: "Heptose" RELATED Unimod-description []
-property_value: DiffAvg "192.17" xsd:float
-property_value: DiffFormula "C 7 H 12 O 6" xsd:string
-property_value: DiffMono "192.063388" xsd:float
-property_value: Formula "C 13 H 24 N 4 O 7" xsd:string
-property_value: MassAvg "348.36" xsd:float
-property_value: MassMono "348.164499" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:490
-is_a: MOD:00925
-
-[Term]
-id: MOD:01200
-name: O-heptosyl-L-threonine
-def: "A protein modification that effectively converts an L-threonine residue to O-heptosyl-L-threonine." [Unimod:490#T]
-comment: From Unimod with no citation [JSG].
-synonym: "Hep" RELATED PSI-MS-label []
-synonym: "Heptose" RELATED Unimod-description []
-property_value: DiffAvg "192.17" xsd:float
-property_value: DiffFormula "C 7 H 12 O 6" xsd:string
-property_value: DiffMono "192.063388" xsd:float
-property_value: Formula "C 11 H 19 N 1 O 8" xsd:string
-property_value: MassAvg "293.27" xsd:float
-property_value: MassMono "293.111067" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:490
-is_a: MOD:00925
-
-[Term]
-id: MOD:01201
-name: N6-heptosyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-heptosyl-L-lysine." [Unimod:490#K]
-comment: From Unimod with no citation [JSG].
-synonym: "Hep" RELATED PSI-MS-label []
-synonym: "Heptose" RELATED Unimod-description []
-property_value: DiffAvg "192.17" xsd:float
-property_value: DiffFormula "C 7 H 12 O 6" xsd:string
-property_value: DiffMono "192.063388" xsd:float
-property_value: Formula "C 13 H 24 N 2 O 7" xsd:string
-property_value: MassAvg "320.34" xsd:float
-property_value: MassMono "320.158351" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:490
-is_a: MOD:00925
-
-[Term]
-id: MOD:01202
-name: N-heptosyl-L-asparagine
-def: "A protein modification that effectively converts an L-asparagine residue to N-heptosyl-L-asparagine." [Unimod:490#N]
-comment: From Unimod with no citation [JSG].
-synonym: "Hep" RELATED PSI-MS-label []
-synonym: "Heptose" RELATED Unimod-description []
-property_value: DiffAvg "192.17" xsd:float
-property_value: DiffFormula "C 7 H 12 O 6" xsd:string
-property_value: DiffMono "192.063388" xsd:float
-property_value: Formula "C 11 H 18 N 2 O 8" xsd:string
-property_value: MassAvg "306.27" xsd:float
-property_value: MassMono "306.106316" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:490
-is_a: MOD:00925
-
-[Term]
-id: MOD:01203
-name: N6-(pyridylacetyl)lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-[(pyrid-3-yl)acetyl]lysine." [PubMed:9276974, Unimod:25#K]
-comment: Produced by reaction with N-[(pyrid-3-yl)acetyl]oxy-succinimide [JSG].
-synonym: "Pyridylacetyl" RELATED PSI-MS-label []
-synonym: "pyridylacetyl" RELATED Unimod-description []
-property_value: DiffAvg "119.12" xsd:float
-property_value: DiffFormula "C 7 H 5 N 1 O 1" xsd:string
-property_value: DiffMono "119.037114" xsd:float
-property_value: Formula "C 13 H 17 N 3 O 2" xsd:string
-property_value: MassAvg "247.30" xsd:float
-property_value: MassMono "247.132077" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:25
-is_a: MOD:00418
-is_a: MOD:01875
-
-[Term]
-id: MOD:01204
-name: prompt loss of methanethiol from oxidixed methionine
-def: "modification from Unimod Artifact -" [PubMed:9004526, Unimod:526]
-synonym: "Dethiomethyl" RELATED PSI-MS-label []
-synonym: "Prompt loss of side chain from oxidised Met" RELATED Unimod-description []
-property_value: DiffAvg "-48.10" xsd:float
-property_value: DiffFormula "C -1 H -4 S -1" xsd:string
-property_value: DiffMono "-48.003371" xsd:float
-property_value: Formula "C 4 H 5 N 1 O 1 S 0" xsd:string
-property_value: MassAvg "83.09" xsd:float
-property_value: MassMono "83.037114" xsd:float
-property_value: Origin "M" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:526
-is_a: MOD:00913
-
-[Term]
-id: MOD:01205
-name: Hex1HexNAc1NeuAc2 O-glycosylated serine
-def: "A protein modification that effectively replaces an O3 hydrogen atom of a serine residue with a carbohydrate-like group composed of Hex1HexNAc1NeuAc2 linked through a glycosidic bond." [PubMed:7949339, Unimod:160#S]
-synonym: "Hex(1)HexNAc(1)NeuAc(2)" RELATED PSI-MS-label []
-synonym: "Hex1HexNAc1NeuAc2" RELATED Unimod-description []
-property_value: DiffAvg "947.85" xsd:float
-property_value: DiffFormula "C 36 H 57 N 3 O 26" xsd:string
-property_value: DiffMono "947.323029" xsd:float
-property_value: Formula "C 39 H 62 N 4 O 28" xsd:string
-property_value: MassAvg "1034.93" xsd:float
-property_value: MassMono "1034.355057" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:160
-is_a: MOD:00528
-is_a: MOD:00916
-
-[Term]
-id: MOD:01206
-name: Hex1HexNAc1NeuAc2 O-glycosylated threonine
-def: "A protein modification that effectively replaces an O3 hydrogen atom of a threonine residue with a carbohydrate-like group composed of Hex1HexNAc1NeuAc2 linked through a glycosidic bond." [Unimod:160#T]
-synonym: "Hex(1)HexNAc(1)NeuAc(2)" RELATED PSI-MS-label []
-synonym: "Hex1HexNAc1NeuAc2" RELATED Unimod-description []
-property_value: DiffAvg "947.85" xsd:float
-property_value: DiffFormula "C 36 H 57 N 3 O 26" xsd:string
-property_value: DiffMono "947.323029" xsd:float
-property_value: Formula "C 40 H 64 N 4 O 28" xsd:string
-property_value: MassAvg "1048.95" xsd:float
-property_value: MassMono "1048.370707" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:160
-is_a: MOD:00528
-is_a: MOD:00005
-
-[Term]
-id: MOD:01207
-name: Hex1HexNAc1NeuAc2 N4-glycosylated asparagine
-def: "A protein modification that effectively replaces an N4 hydrogen atom of an asparagine residue with a carbohydrate-like group composed of Hex1HexNAc1NeuAc2 linked through a glycosidic bond." [Unimod:160#N]
-synonym: "Hex(1)HexNAc(1)NeuAc(2)" RELATED PSI-MS-label []
-synonym: "Hex1HexNAc1NeuAc2" RELATED Unimod-description []
-property_value: DiffAvg "947.85" xsd:float
-property_value: DiffFormula "C 36 H 57 N 3 O 26" xsd:string
-property_value: DiffMono "947.323029" xsd:float
-property_value: Formula "C 40 H 63 N 5 O 28" xsd:string
-property_value: MassAvg "1061.95" xsd:float
-property_value: MassMono "1061.365956" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:160
-is_a: MOD:00528
-is_a: MOD:00160
-
-[Term]
-id: MOD:01208
-name: copper(1+) carboxylate C-terminal residue
-def: "A protein modification that effectively converts a C-terminal residue to the copper(1+) carboxylate salt." [Unimod:531#C-term]
-synonym: "Cation:Cu[I]" RELATED PSI-MS-label []
-synonym: "cuprous salt" EXACT PSI-MOD-alternate []
-synonym: "Replacement of proton by copper" RELATED Unimod-description []
-property_value: DiffAvg "62.54" xsd:float
-property_value: DiffFormula "Cu 1 H -1" xsd:string
-property_value: DiffMono "61.921772" xsd:float
-property_value: Origin "X" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: Unimod:531
-is_a: MOD:00742
-
-[Term]
-id: MOD:01209
-name: copper(1+) L-aspartate
-def: "A protein modification that effectively converts an L-aspartic acid residue to the copper(1+) aspartate salt." [Unimod:531#D]
-synonym: "Cation:Cu[I]" RELATED PSI-MS-label []
-synonym: "cuprous salt" EXACT PSI-MOD-alternate []
-synonym: "Replacement of proton by copper" RELATED Unimod-description []
-property_value: DiffAvg "62.54" xsd:float
-property_value: DiffFormula "Cu 1 H -1" xsd:string
-property_value: DiffMono "61.921772" xsd:float
-property_value: Formula "C 4 Cu 1 H 4 N 1 O 3" xsd:string
-property_value: MassAvg "177.63" xsd:float
-property_value: MassMono "176.948715" xsd:float
-property_value: Origin "D" xsd:string
-xref: Unimod:531
-is_a: MOD:00742
-is_a: MOD:02066
-
-[Term]
-id: MOD:01210
-name: copper(1+) L-glutamate
-def: "A protein modification that effectively converts an L-glutamic acid residue to the copper(1+) glutamate salt." [Unimod:531#E]
-synonym: "Cation:Cu[I]" RELATED PSI-MS-label []
-synonym: "cuprous salt" EXACT PSI-MOD-alternate []
-synonym: "Replacement of proton by copper" RELATED Unimod-description []
-property_value: DiffAvg "62.54" xsd:float
-property_value: DiffFormula "Cu 1 H -1" xsd:string
-property_value: DiffMono "61.921772" xsd:float
-property_value: Formula "C 5 Cu 1 H 6 N 1 O 3" xsd:string
-property_value: MassAvg "191.65" xsd:float
-property_value: MassMono "190.964366" xsd:float
-property_value: Origin "E" xsd:string
-xref: Unimod:531
-is_a: MOD:00742
-is_a: MOD:02068
-
-[Term]
-id: MOD:01211
-name: N6-(morpholine-2-acetyl)-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-(morpholine-2-acetyl)-lysine." [PubMed:10446193, Unimod:29#K]
-comment: The Unimod name \"N-Succinimidyl-3-morpholine acetate\" appears to have been a typographical error [JSG].
-synonym: "N-Succinimidyl-2-morpholine acetate" RELATED Unimod-description []
-synonym: "N-succinimidylmorpholine-2-acetate N6-derivatized lysine" EXACT PSI-MOD-alternate []
-synonym: "SMA" RELATED PSI-MS-label []
-property_value: DiffAvg "127.14" xsd:float
-property_value: DiffFormula "C 6 H 9 N 1 O 2" xsd:string
-property_value: DiffMono "127.063329" xsd:float
-property_value: Formula "C 12 H 21 N 3 O 3" xsd:string
-property_value: MassAvg "255.32" xsd:float
-property_value: MassMono "255.158292" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:29
-is_a: MOD:01813
-is_a: MOD:01875
-
-[Term]
-id: MOD:01212
-name: iodoacetamide N6-derivatized lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-(carboxamidomethyl)lysine." [OMSSA:27, PubMed:11510821, PubMed:12422359, PubMed:12686488, Unimod:4#K]
-subset: PSI-MOD-slim
-synonym: "Carbamidomethyl" RELATED PSI-MS-label []
-synonym: "carbamidomethylk" EXACT OMSSA-label []
-synonym: "Iodoacetamide derivative" RELATED Unimod-description []
-synonym: "N6-(2-amino-2-oxoethyl)lysine" EXACT PSI-MOD-alternate []
-synonym: "N6-(carbamoylmethyl)lysine" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "57.05" xsd:float
-property_value: DiffFormula "C 2 H 3 N 1 O 1" xsd:string
-property_value: DiffMono "57.021464" xsd:float
-property_value: Formula "C 8 H 15 N 3 O 2" xsd:string
-property_value: MassAvg "185.23" xsd:float
-property_value: MassMono "185.116427" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:4
-is_a: MOD:00397
-is_a: MOD:00912
-
-[Term]
-id: MOD:01213
-name: iodoacetamide derivatized histidine
-def: "A protein modification that effectively converts an L-histidine residue to an iodoacetamide derivatized histidine, either 1'- or 3'-(carboxamidolmethyl)histidine." [OMSSA:28, PubMed:11510821, PubMed:12422359, PubMed:15627961, PubMed:2026710, Unimod:4#H]
-subset: PSI-MOD-slim
-synonym: "Carbamidomethyl" RELATED PSI-MS-label []
-synonym: "carbamidometylh" EXACT OMSSA-label []
-synonym: "Iodoacetamide derivative" RELATED Unimod-description []
-property_value: DiffAvg "57.05" xsd:float
-property_value: DiffFormula "C 2 H 3 N 1 O 1" xsd:string
-property_value: DiffMono "57.021464" xsd:float
-property_value: Formula "C 8 H 10 N 4 O 2" xsd:string
-property_value: MassAvg "194.19" xsd:float
-property_value: MassMono "194.080376" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:4
-is_a: MOD:00397
-is_a: MOD:00909
-
-[Term]
-id: MOD:01214
-name: iodoacetamide - site C
-def: "modification from Unimod Chemical derivative - OBSOLETE because redundant, the difference component of MOD:01060. Remap to MOD:01060." [PubMed:10504701, PubMed:11510821, PubMed:12422359, Unimod:4#C]
-synonym: "Carbamidomethyl" RELATED PSI-MS-label []
-synonym: "Iodoacetamide derivative" RELATED Unimod-description []
-property_value: DiffAvg "57.05" xsd:float
-property_value: DiffFormula "C 2 H 3 N 1 O 1" xsd:string
-property_value: DiffMono "57.021464" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-replaced_by: MOD:01060
-xref: Unimod:4
-is_obsolete: true
-
-[Term]
-id: MOD:01215
-name: iodoacetamide derivatized aspartic acid
-def: "A protein modification that effectively converts an L-aspartic acid residue to O4-(carboxamidomethyl)aspartate." [OMSSA:29, PubMed:11510821, PubMed:12422359, PubMed:16526082, Unimod:4#D]
-subset: PSI-MOD-slim
-synonym: "Carbamidomethyl" RELATED PSI-MS-label []
-synonym: "carbamidomethyld" EXACT OMSSA-label []
-synonym: "Iodoacetamide derivative" RELATED Unimod-description []
-property_value: DiffAvg "57.05" xsd:float
-property_value: DiffFormula "C 2 H 3 N 1 O 1" xsd:string
-property_value: DiffMono "57.021464" xsd:float
-property_value: Formula "C 6 H 8 N 2 O 4" xsd:string
-property_value: MassAvg "172.14" xsd:float
-property_value: MassMono "172.048407" xsd:float
-property_value: Origin "D" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:4
-is_a: MOD:00397
-is_a: MOD:00904
-
-[Term]
-id: MOD:01216
-name: iodoacetamide derivatized glutamic acid
-def: "A protein modification that effectively converts an L-glutamic acid residue to O5-(carboxamidomethyl)glutamate." [OMSSA:30, PubMed:11510821, PubMed:12422359, Unimod:4#E]
-subset: PSI-MOD-slim
-synonym: "Carbamidomethyl" RELATED PSI-MS-label []
-synonym: "carbamidomethyle" EXACT OMSSA-label []
-synonym: "Iodoacetamide derivative" RELATED Unimod-description []
-property_value: DiffAvg "57.05" xsd:float
-property_value: DiffFormula "C 2 H 3 N 1 O 1" xsd:string
-property_value: DiffMono "57.021464" xsd:float
-property_value: Formula "C 7 H 10 N 2 O 4" xsd:string
-property_value: MassAvg "186.17" xsd:float
-property_value: MassMono "186.064057" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:4
-is_a: MOD:00397
-is_a: MOD:00906
-
-[Term]
-id: MOD:01217
-name: Sulfanilic Acid (SA), light C12 - site D
-def: "modification from Unimod Isotopic label -" [PubMed:12872131, Unimod:285#D]
-synonym: "Light Sulfanilic Acid (SA) C12" RELATED Unimod-description []
-synonym: "SulfanilicAcid" RELATED PSI-MS-label []
-property_value: DiffAvg "155.00" xsd:float
-property_value: DiffFormula "(12)C 6 H 5 N 1 O 2 S 1" xsd:string
-property_value: DiffMono "155.004099" xsd:float
-property_value: Formula "(12)C 10 H 10 N 2 O 5 S 1" xsd:string
-property_value: MassAvg "270.03" xsd:float
-property_value: MassMono "270.031042" xsd:float
-property_value: Origin "D" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:285
-is_a: MOD:00605
-
-[Term]
-id: MOD:01218
-name: Sulfanilic Acid (SA), light C12 - site E
-def: "modification from Unimod Isotopic label -" [PubMed:15283597, Unimod:285#E]
-synonym: "Light Sulfanilic Acid (SA) C12" RELATED Unimod-description []
-synonym: "SulfanilicAcid" RELATED PSI-MS-label []
-property_value: DiffAvg "155.00" xsd:float
-property_value: DiffFormula "(12)C 6 H 5 N 1 O 2 S 1" xsd:string
-property_value: DiffMono "155.004099" xsd:float
-property_value: Formula "(12)C 11 H 12 N 2 O 5 S 1" xsd:string
-property_value: MassAvg "284.05" xsd:float
-property_value: MassMono "284.046692" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:285
-is_a: MOD:00605
-
-[Term]
-id: MOD:01219
-name: Sulfanilic Acid (SA), heavy C13 - site D
-def: "modification from Unimod Chemical derivative -" [PubMed:9254591, PubMed:9750125, Unimod:286#D]
-synonym: "Heavy Sulfanilic Acid (SA) C13" RELATED Unimod-description []
-synonym: "SulfanilicAcid:13C(6)" RELATED PSI-MS-label []
-property_value: DiffAvg "161.02" xsd:float
-property_value: DiffFormula "(13)C 6 H 5 N 1 O 2 S 1" xsd:string
-property_value: DiffMono "161.024228" xsd:float
-property_value: Formula "(12)C 4 (13)C 6 H 10 N 2 O 5 S 1" xsd:string
-property_value: MassAvg "276.05" xsd:float
-property_value: MassMono "276.051171" xsd:float
-property_value: Origin "D" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:286
-is_a: MOD:00606
-
-[Term]
-id: MOD:01220
-name: Sulfanilic Acid (SA), heavy C13 - site E
-def: "modification from Unimod Chemical derivative -" [PubMed:15121203, PubMed:9254591, Unimod:286#E]
-synonym: "Heavy Sulfanilic Acid (SA) C13" RELATED Unimod-description []
-synonym: "SulfanilicAcid:13C(6)" RELATED PSI-MS-label []
-property_value: DiffAvg "161.02" xsd:float
-property_value: DiffFormula "(13)C 6 H 5 N 1 O 2 S 1" xsd:string
-property_value: DiffMono "161.024228" xsd:float
-property_value: Formula "(12)C 5 (13)C 6 H 12 N 2 O 5 S 1" xsd:string
-property_value: MassAvg "290.07" xsd:float
-property_value: MassMono "290.066822" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:286
-is_a: MOD:00606
-
-[Term]
-id: MOD:01221
-name: O-formyl-L-threonine
-def: "A protein modification that effectively converts an L-threonine residue to O-formyl-L-threonine." [PubMed:11861642, PubMed:15799070, Unimod:122#T]
-comment: From Unimod: Can occur under CNBr cleavage conditions (70% HCOOH).
-synonym: "Formyl" RELATED PSI-MS-label []
-synonym: "Formylation" RELATED Unimod-description []
-property_value: DiffAvg "28.01" xsd:float
-property_value: DiffFormula "C 1 O 1" xsd:string
-property_value: DiffMono "27.994915" xsd:float
-property_value: Formula "C 5 H 7 N 1 O 3" xsd:string
-property_value: MassAvg "129.12" xsd:float
-property_value: MassMono "129.042593" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:122
-is_a: MOD:02004
-is_a: MOD:01483
-
-[Term]
-id: MOD:01222
-name: O-formyl-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O-formyl-L-serine." [PubMed:15627961, PubMed:15799070, Unimod:122#S]
-comment: From Unimod: Can occur under CNBr cleavage conditions (70% HCOOH).
-synonym: "Formyl" RELATED PSI-MS-label []
-synonym: "Formylation" RELATED Unimod-description []
-property_value: DiffAvg "28.01" xsd:float
-property_value: DiffFormula "C 1 O 1" xsd:string
-property_value: DiffMono "27.994915" xsd:float
-property_value: Formula "C 4 H 5 N 1 O 3" xsd:string
-property_value: MassAvg "115.09" xsd:float
-property_value: MassMono "115.026943" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:122
-is_a: MOD:02003
-is_a: MOD:01483
-
-[Term]
-id: MOD:01223
-name: thioacylation of primary amines - site N-term
-def: "modification from Unimod Other -" [OMSSA:41, PubMed:11710128, PubMed:3155470, PubMed:957432, Unimod:126#N-term]
-comment: This Unimod entry is misdescribed as \"thioacylation\" [JSG].
-synonym: "3,3-Dithio-bis-(sulfosuccinimidyl)propionate" RELATED Unimod-alternate []
-synonym: "ntermpeptioacetyl" EXACT OMSSA-label []
-synonym: "Thioacyl" RELATED PSI-MS-label []
-synonym: "thioacylation of primary amines (N-term and Lys)" RELATED Unimod-description []
-property_value: DiffAvg "88.12" xsd:float
-property_value: DiffFormula "C 3 H 4 O 1 S 1" xsd:string
-property_value: DiffMono "87.998286" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:126
-is_a: MOD:00497
-
-[Term]
-id: MOD:01224
-name: thioacylation of primary amines - site K
-def: "modification from Unimod Other -" [OMSSA:40, PubMed:11710128, PubMed:3155470, PubMed:957432, Unimod:126#K]
-comment: This Unimod entry is misdescribed as \"thioacylation\" [JSG].
-synonym: "3,3-Dithio-bis-(sulfosuccinimidyl)propionate" RELATED Unimod-alternate []
-synonym: "thioacetylk" EXACT OMSSA-label []
-synonym: "Thioacyl" RELATED PSI-MS-label []
-synonym: "thioacylation of primary amines (N-term and Lys)" RELATED Unimod-description []
-property_value: DiffAvg "88.12" xsd:float
-property_value: DiffFormula "C 3 H 4 O 1 S 1" xsd:string
-property_value: DiffMono "87.998286" xsd:float
-property_value: Formula "C 9 H 16 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "216.30" xsd:float
-property_value: MassMono "216.093249" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:126
-is_a: MOD:00497
-
-[Term]
-id: MOD:01225
-name: monofluorinated L-tyrosine
-def: "A protein modification that effectively converts an L-tyrosine residue into an L-fluorotyrosine." [OMSSA:46, PubMed:8069568, Unimod:127#Y]
-comment: From Unimod: the citation appears to be correct, but the PMID is not and has been corrected [JSG].
-synonym: "Fluoro" RELATED PSI-MS-label []
-synonym: "fluorophenylalanine replacement of phenylalanine" RELATED Unimod-description []
-synonym: "phef" EXACT OMSSA-label []
-property_value: DiffAvg "17.99" xsd:float
-property_value: DiffFormula "F 1 H -1" xsd:string
-property_value: DiffMono "17.990578" xsd:float
-property_value: Formula "C 9 F 1 H 8 N 1 O 2" xsd:string
-property_value: MassAvg "181.17" xsd:float
-property_value: MassMono "181.053907" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:127
-is_a: MOD:00498
-is_a: MOD:00985
-
-[Term]
-id: MOD:01226
-name: monofluorinated L-tryptophan
-def: "A protein modification that effectively converts an L-tryptophan residue to an L-fluorotryptophan." [PubMed:8069568, Unimod:127#W]
-comment: From Unimod: the citation appears to be correct, but the PMID is not and has been corrected [JSG].
-synonym: "Fluoro" RELATED PSI-MS-label []
-synonym: "fluorophenylalanine replacement of phenylalanine" RELATED Unimod-description []
-property_value: DiffAvg "17.99" xsd:float
-property_value: DiffFormula "F 1 H -1" xsd:string
-property_value: DiffMono "17.990578" xsd:float
-property_value: Formula "C 11 F 1 H 9 N 2 O 1" xsd:string
-property_value: MassAvg "204.20" xsd:float
-property_value: MassMono "204.069891" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:127
-is_a: MOD:00498
-is_a: MOD:01068
-
-[Term]
-id: MOD:01227
-name: monofluorinated L-phenylalanine
-def: "A protein modification that effectively converts an L-phenylalanine residue to an L-fluorophenylalanine." [DeltaMass:181, OMSSA:46, PubMed:8069568, Unimod:127#F]
-comment: From Unimod: the citation appears to be correct, but the PMID is not and has been corrected. From DeltaMass: (element abbreviation in formula incorrect, mass incorrect, and aggregate not delta) Average Mass: 149 Formula: C9H8O1N1Fl1 Average Mass Change: 149 References:PE Sciex with no citation [JSG].
-synonym: "Fluoro" RELATED PSI-MS-label []
-synonym: "fluorophenylalanine replacement of phenylalanine" RELATED Unimod-description []
-synonym: "phef" EXACT OMSSA-label []
-property_value: DiffAvg "17.99" xsd:float
-property_value: DiffFormula "C 0 F 1 H -1 N 0 O 0" xsd:string
-property_value: DiffMono "17.990578" xsd:float
-property_value: Formula "C 9 F 1 H 8 N 1 O 1" xsd:string
-property_value: MassAvg "165.17" xsd:float
-property_value: MassMono "165.058992" xsd:float
-property_value: Origin "F" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:127
-is_a: MOD:00498
-is_a: MOD:01066
-
-[Term]
-id: MOD:01228
-name: monoiodinated tyrosine
-def: "A protein modification that effectively substitutes one hydrogen atom of an L-tyrosine residue with one iodine atom." [DeltaMass:0, OMSSA:65, PubMed:1326520, PubMed:15627961, PubMed:2026710, Unimod:129#Y]
-comment: From DeltaMass: Average Mass: 289 [name misspelled \"monoiodated\" - JSG].
-subset: PSI-MOD-slim
-synonym: "I1Tyr" EXACT PSI-MOD-label []
-synonym: "Iodination" RELATED Unimod-description []
-synonym: "iodinationy" EXACT OMSSA-label []
-synonym: "Iodo" RELATED PSI-MS-label []
-property_value: DiffAvg "125.90" xsd:float
-property_value: DiffFormula "H -1 I 1" xsd:string
-property_value: DiffMono "125.896648" xsd:float
-property_value: Formula "C 9 H 8 I 1 N 1 O 2" xsd:string
-property_value: MassAvg "289.07" xsd:float
-property_value: MassMono "288.959976" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:129
-is_a: MOD:00500
-is_a: MOD:00998
-
-[Term]
-id: MOD:01229
-name: L-iodohistidine
-def: "A protein modification that effectively converts an L-histidine residue to an L-iodohistidine." [PubMed:15627961, PubMed:2026710, Unimod:129#H]
-synonym: "I1His" EXACT PSI-MOD-label []
-synonym: "Iodination" RELATED Unimod-description []
-synonym: "Iodo" RELATED PSI-MS-label []
-property_value: DiffAvg "125.90" xsd:float
-property_value: DiffFormula "C 0 H -1 I 1 N 0 O 0" xsd:string
-property_value: DiffMono "125.896648" xsd:float
-property_value: Formula "C 6 H 6 I 1 N 3 O 1" xsd:string
-property_value: MassAvg "263.04" xsd:float
-property_value: MassMono "262.955560" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:129
-is_a: MOD:00500
-is_a: MOD:01049
-
-[Term]
-id: MOD:01230
-name: Bruker Daltonics SERVA-ICPL(TM) quantification chemistry, light form - site K
-def: "modification from Unimod Isotopic label -" [PubMed:15602776, Unimod:365#K]
-synonym: "Bruker Daltonics SERVA-ICPL(TM) quantification chemistry, light form" RELATED Unimod-description []
-synonym: "ICPL" RELATED PSI-MS-label []
-property_value: DiffAvg "105.02" xsd:float
-property_value: DiffFormula "(12)C 6 H 3 N 1 O 1" xsd:string
-property_value: DiffMono "105.021464" xsd:float
-property_value: Formula "(12)C 12 H 15 N 3 O 2" xsd:string
-property_value: MassAvg "233.12" xsd:float
-property_value: MassMono "233.116427" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:365
-is_a: MOD:00790
-
-[Term]
-id: MOD:01231
-name: 3x(13)C labeled N6-propanoyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to 3x(13)C labeled N6-propanoyl-L-lysine." [PubMed:11857757, PubMed:11999733, PubMed:12175151, PubMed:12442261, Unimod:59#K]
-subset: PSI-MOD-slim
-synonym: "Propionate labeling reagent heavy form (+3amu), N-term & K" RELATED Unimod-description []
-synonym: "Propionyl:13C(3)" RELATED PSI-MS-label []
-property_value: DiffAvg "59.04" xsd:float
-property_value: DiffFormula "(13)C 3 H 4 O 1" xsd:string
-property_value: DiffMono "59.036279" xsd:float
-property_value: Formula "(12)C 6 (13)C 3 H 16 N 2 O 2" xsd:string
-property_value: MassAvg "187.13" xsd:float
-property_value: MassMono "187.131242" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:59
-relationship: derives_from MOD:01398
-is_a: MOD:01428
-
-[Term]
-id: MOD:01232
-name: 3x(12)C labeled N6-propanoyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to 3x(12)C labeled N6-propanoyl-L-lysine." [PubMed:11857757, PubMed:11999733, PubMed:12175151, Unimod:58#K]
-subset: PSI-MOD-slim
-synonym: "Propionate labeling reagent light form (N-term & K)" RELATED Unimod-description []
-synonym: "Propionyl" RELATED PSI-MS-label []
-property_value: DiffAvg "56.03" xsd:float
-property_value: DiffFormula "(12)C 3 H 4 O 1" xsd:string
-property_value: DiffMono "56.026215" xsd:float
-property_value: Formula "(12)C 9 H 16 N 2 O 2" xsd:string
-property_value: MassAvg "184.12" xsd:float
-property_value: MassMono "184.121178" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:58
-relationship: derives_from MOD:01398
-is_a: MOD:01426
-
-[Term]
-id: MOD:01233
-name: 3x(2)H labeled N6-acetyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to 3x(2)H labeled N6-acetyl-L-lysine." [PubMed:11857757, PubMed:11999733, PubMed:12175151, Unimod:56#K]
-subset: PSI-MOD-slim
-synonym: "Acetate labeling reagent (N-term & K) (heavy form, +3amu)" RELATED Unimod-description []
-synonym: "Acetyl:2H(3)" RELATED PSI-MS-label []
-property_value: DiffAvg "45.03" xsd:float
-property_value: DiffFormula "C 2 (1)H -1 (2)H 3 O 1" xsd:string
-property_value: DiffMono "45.029395" xsd:float
-property_value: Formula "C 8 (1)H 11 (2)H 3 N 2 O 2" xsd:string
-property_value: MassAvg "173.12" xsd:float
-property_value: MassMono "173.124358" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:56
-relationship: derives_from MOD:00064
-is_a: MOD:00449
-
-[Term]
-id: MOD:01234
-name: (18)O monosubstituted L-serine
-def: "modification from Unimod Isotopic label - alkaline phosphatase to dephosphorylate" [PubMed:11467524, Unimod:258#S]
-subset: PSI-MOD-slim
-synonym: "Label:18O(1)" RELATED PSI-MS-label []
-synonym: "O18 Labeling" RELATED Unimod-description []
-property_value: DiffAvg "2.00" xsd:float
-property_value: DiffFormula "(16)O -1 (18)O 1" xsd:string
-property_value: DiffMono "2.004246" xsd:float
-property_value: Formula "C 3 H 5 N 1 (16)O 1 (18)O 1" xsd:string
-property_value: MassAvg "89.04" xsd:float
-property_value: MassMono "89.036275" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:258
-is_a: MOD:00581
-is_a: MOD:00916
-
-[Term]
-id: MOD:01235
-name: (18)O monosubstituted L-threonine
-def: "modification from Unimod Isotopic label - alkaline phosphatase to dephosphorylate" [PubMed:11467524, PubMed:15549660, Unimod:258#T]
-subset: PSI-MOD-slim
-synonym: "Label:18O(1)" RELATED PSI-MS-label []
-synonym: "O18 Labeling" RELATED Unimod-description []
-property_value: DiffAvg "2.00" xsd:float
-property_value: DiffFormula "(16)O -1 (18)O 1" xsd:string
-property_value: DiffMono "2.004246" xsd:float
-property_value: Formula "C 4 H 7 N 1 (16)O 1 (18)O 1" xsd:string
-property_value: MassAvg "103.05" xsd:float
-property_value: MassMono "103.051925" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:258
-is_a: MOD:00581
-is_a: MOD:00917
-
-[Term]
-id: MOD:01236
-name: (18)O monosubstituted L-tyrosine
-def: "modification from Unimod Isotopic label - alkaline phosphatase to dephosphorylate" [PubMed:11467524, PubMed:15549660, Unimod:258#Y]
-subset: PSI-MOD-slim
-synonym: "Label:18O(1)" RELATED PSI-MS-label []
-synonym: "O18 Labeling" RELATED Unimod-description []
-property_value: DiffAvg "2.00" xsd:float
-property_value: DiffFormula "(16)O -1 (18)O 1" xsd:string
-property_value: DiffMono "2.004246" xsd:float
-property_value: Formula "C 9 H 9 N 1 (16)O 1 (18)O 1" xsd:string
-property_value: MassAvg "165.07" xsd:float
-property_value: MassMono "165.067575" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:258
-is_a: MOD:00581
-is_a: MOD:00919
-
-[Term]
-id: MOD:01237
-name: cysteine 4-hydroxynonenal adduct
-def: "A protein modification produced by formation of an adduct of an L-cysteine residue with 4-hydroxynonenal." [PubMed:11327326, PubMed:15133838, PubMed:9629898, Unimod:53#C]
-comment: 4-hydroxynonenal, a toxic lipid aldehyde, is a product of the hydroperoxide beta-cleavage degradation of omega-6 polyunsaturated fatty acids, such as arachidonic and linoleic acids [JSG].
-synonym: "4-hydroxynonenal (HNE)" RELATED Unimod-description []
-synonym: "HNE" RELATED PSI-MS-label []
-property_value: DiffAvg "156.22" xsd:float
-property_value: DiffFormula "C 9 H 16 O 2" xsd:string
-property_value: DiffMono "156.115030" xsd:float
-property_value: Formula "C 12 H 21 N 1 O 3 S 1" xsd:string
-property_value: MassAvg "259.36" xsd:float
-property_value: MassMono "259.124215" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:53
-is_a: MOD:00446
-
-[Term]
-id: MOD:01238
-name: lysine 4-hydroxynonenal adduct
-def: "A protein modification produced by formation of an adduct of an L-lysine residue with 4-hydroxynonenal." [PubMed:11327326, PubMed:15133838, PubMed:9629898, Unimod:53#K]
-comment: 4-hydroxynonenal, a toxic lipid aldehyde, is a product of the hydroperoxide beta-cleavage degradation of omega-6 polyunsaturated fatty acids, such as arachidonic and linoleic acids [JSG].
-synonym: "4-hydroxynonenal (HNE)" RELATED Unimod-description []
-synonym: "HNE" RELATED PSI-MS-label []
-property_value: DiffAvg "156.22" xsd:float
-property_value: DiffFormula "C 9 H 16 O 2" xsd:string
-property_value: DiffMono "156.115030" xsd:float
-property_value: Formula "C 15 H 28 N 2 O 3" xsd:string
-property_value: MassAvg "284.40" xsd:float
-property_value: MassMono "284.209993" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:53
-is_a: MOD:00446
-
-[Term]
-id: MOD:01239
-name: histidine 4-hydroxynonenal adduct
-def: "A protein modification produced by formation of an adduct of an L-histidine residue with 4-hydroxynonenal." [PubMed:10717661, PubMed:11327326, PubMed:15133838, Unimod:53#H]
-comment: 4-hydroxynonenal, a toxic lipid aldehyde, is a product of the hydroperoxide beta-cleavage degradation of omega-6 polyunsaturated fatty acids, such as arachidonic and linoleic acids [JSG].
-synonym: "4-hydroxynonenal (HNE)" RELATED Unimod-description []
-synonym: "HNE" RELATED PSI-MS-label []
-property_value: DiffAvg "156.22" xsd:float
-property_value: DiffFormula "C 9 H 16 O 2" xsd:string
-property_value: DiffMono "156.115030" xsd:float
-property_value: Formula "C 15 H 23 N 3 O 3" xsd:string
-property_value: MassAvg "293.37" xsd:float
-property_value: MassMono "293.173942" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:53
-is_a: MOD:00446
-
-[Term]
-id: MOD:01240
-name: ubiquitination signature tetrapeptidyl lysine
-def: "A protein modification that crosslinks the N6-amino of a peptidyl lysine with the carboxyl of leucyl-arginyl-glycyl-glycine, the C-terminal tetrapeptide of ubiquitin." [PubMed:10504701, Unimod:535]
-synonym: "LeuArgGlyGly" RELATED PSI-MS-label []
-synonym: "Ubiquitination" RELATED Unimod-description []
-property_value: DiffAvg "383.45" xsd:float
-property_value: DiffFormula "C 16 H 29 N 7 O 4" xsd:string
-property_value: DiffMono "383.228102" xsd:float
-property_value: Formula "C 22 H 41 N 9 O 5" xsd:string
-property_value: MassAvg "511.63" xsd:float
-property_value: MassMono "511.323065" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:535
-is_a: MOD:02047
-is_a: MOD:02051
-is_a: MOD:01875
-relationship: derives_from MOD:01148
-
-[Term]
-id: MOD:01241
-name: 3x(2)H labeled L-aspartic acid 4-methyl ester
-def: "A protein modification that effectively converts an L-lysine residue to 3x(2)H labeled L-aspartic acid 4-methyl ester." [OMSSA:19, PubMed:12185208, Unimod:298#D]
-synonym: "deuterated methyl ester" RELATED Unimod-description []
-synonym: "Methyl:2H(3)" RELATED PSI-MS-label []
-synonym: "trideuteromethyld" EXACT OMSSA-label []
-property_value: DiffAvg "17.03" xsd:float
-property_value: DiffFormula "C 1 (1)H -1 (2)H 3" xsd:string
-property_value: DiffMono "17.034480" xsd:float
-property_value: Formula "C 5 (1)H 4 (2)H 3 N 1 O 3" xsd:string
-property_value: MassAvg "132.06" xsd:float
-property_value: MassMono "132.061423" xsd:float
-property_value: Origin "D" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:298
-is_a: MOD:00617
-is_a: MOD:00904
-relationship: derives_from MOD:01181
-
-[Term]
-id: MOD:01242
-name: 3x(2)H labeled L-glutamic acid 5-methyl ester
-def: "A protein modification that effectively converts an L-lysine residue to 3x(2)H labeled L-glutamic acid 5-methyl ester." [OMSSA:20, PubMed:1326520, Unimod:298#E]
-synonym: "deuterated methyl ester" RELATED Unimod-description []
-synonym: "Methyl:2H(3)" RELATED PSI-MS-label []
-synonym: "trideuteromethyle" EXACT OMSSA-label []
-property_value: DiffAvg "17.03" xsd:float
-property_value: DiffFormula "C 1 (1)H -1 (2)H 3" xsd:string
-property_value: DiffMono "17.034480" xsd:float
-property_value: Formula "C 6 (1)H 6 (2)H 3 N 1 O 3" xsd:string
-property_value: MassAvg "146.08" xsd:float
-property_value: MassMono "146.077073" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:298
-is_a: MOD:00617
-is_a: MOD:00906
-relationship: derives_from MOD:00081
-
-[Term]
-id: MOD:01243
-name: potassium carboxylate C-terminal residue
-def: "A protein modification that effectively converts a C-terminal residue to the potassium carboxylate salt." [Unimod:530#C-term]
-synonym: "Cation:K" RELATED PSI-MS-label []
-synonym: "Replacement of proton by potassium" RELATED Unimod-description []
-property_value: DiffAvg "38.09" xsd:float
-property_value: DiffFormula "H -1 K 1" xsd:string
-property_value: DiffMono "37.955882" xsd:float
-property_value: Origin "X" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: Unimod:530
-is_a: MOD:01072
-
-[Term]
-id: MOD:01244
-name: potassium L-glutamate
-def: "A protein modification that effectively converts an L-glutamioc acid residue to the potassium glutamate salt." [Unimod:530#E]
-synonym: "Cation:K" RELATED PSI-MS-label []
-synonym: "Replacement of proton by potassium" RELATED Unimod-description []
-property_value: DiffAvg "38.09" xsd:float
-property_value: DiffFormula "H -1 K 1" xsd:string
-property_value: DiffMono "37.955882" xsd:float
-property_value: Formula "C 5 H 6 K 1 N 1 O 3" xsd:string
-property_value: MassAvg "167.21" xsd:float
-property_value: MassMono "166.998475" xsd:float
-property_value: Origin "E" xsd:string
-xref: Unimod:530
-is_a: MOD:00906
-is_a: MOD:01072
-
-[Term]
-id: MOD:01245
-name: potassium L-aspartate
-def: "A protein modification that effectively converts an L-aspartic acid residue to the potassium aspartate salt." [Unimod:530#D]
-synonym: "Cation:K" RELATED PSI-MS-label []
-synonym: "Replacement of proton by potassium" RELATED Unimod-description []
-property_value: DiffAvg "38.09" xsd:float
-property_value: DiffFormula "H -1 K 1" xsd:string
-property_value: DiffMono "37.955882" xsd:float
-property_value: Formula "C 4 H 4 K 1 N 1 O 3" xsd:string
-property_value: MassAvg "153.18" xsd:float
-property_value: MassMono "152.982825" xsd:float
-property_value: Origin "D" xsd:string
-xref: Unimod:530
-is_a: MOD:00904
-is_a: MOD:01072
-
-[Term]
-id: MOD:01246
-name: fucosylated -site S
-def: "OBSOLETE because redundant and identical to MOD:00812 after formula correction. Remap to MOD:00812." [PubMed:11344537, PubMed:15189151, PubMed:3311742, PubMed:3578767, Unimod:295#S]
-synonym: "dHex" RELATED PSI-MS-label []
-synonym: "Fucose" RELATED Unimod-description []
-property_value: DiffAvg "147.15" xsd:float
-property_value: DiffFormula "C 6 H 11 O 4" xsd:string
-property_value: DiffMono "147.065734" xsd:float
-property_value: Formula "C 9 H 16 N 1 O 6" xsd:string
-property_value: MassAvg "234.23" xsd:float
-property_value: MassMono "234.097762" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-replaced_by: MOD:00812
-xref: Unimod:295
-is_obsolete: true
-
-[Term]
-id: MOD:01247
-name: fucosylated -site T
-def: "OBSOLETE because redundant and identical to MOD:00813 after formula correction. Remap to MOD:00813." [PubMed:11344537, PubMed:11857757, PubMed:15189151, Unimod:295#T]
-synonym: "dHex" RELATED PSI-MS-label []
-synonym: "Fucose" RELATED Unimod-description []
-property_value: DiffAvg "147.15" xsd:float
-property_value: DiffFormula "C 6 H 11 O 4" xsd:string
-property_value: DiffMono "147.065734" xsd:float
-property_value: Formula "C 10 H 18 N 1 O 6" xsd:string
-property_value: MassAvg "248.26" xsd:float
-property_value: MassMono "248.113412" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-replaced_by: MOD:00813
-xref: Unimod:295
-is_obsolete: true
-
-[Term]
-id: MOD:01248
-name: iodouridine monophosphate derivatized tyrosine
-def: "A protein modification that is produced by reaction of iodouridine monophosphate with an L-tyrosine residue to form an ether linkage." [PubMed:11112526, PubMed:11567090, PubMed:6540775, Unimod:292#Y]
-comment: This has an ether linkage and not a phosphodiester linkage with UMP.
-synonym: "Cross-link of (Iodo)-uracil MP with W,F,Y" RELATED Unimod-description []
-synonym: "IodoU-AMP" RELATED PSI-MS-label []
-property_value: DiffAvg "322.17" xsd:float
-property_value: DiffFormula "C 9 H 11 N 2 O 9 P 1" xsd:string
-property_value: DiffMono "322.020217" xsd:float
-property_value: Formula "C 18 H 20 N 3 O 11 P 1" xsd:string
-property_value: MassAvg "485.34" xsd:float
-property_value: MassMono "485.083545" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:292
-is_a: MOD:00611
-is_a: MOD:00919
-
-[Term]
-id: MOD:01249
-name: iodouridine monophosphate derivatized tryptophan
-def: "A protein modification that is produced by reaction of iodouridine monophosphate with an L-tryptophan residue." [PubMed:11112526, PubMed:11567090, PubMed:6540775, Unimod:292#W]
-comment: This has a carbon-nitrogen linkage and not a phosphodiester linkage with UMP.
-synonym: "Cross-link of (Iodo)-uracil MP with W,F,Y" RELATED Unimod-description []
-synonym: "IodoU-AMP" RELATED PSI-MS-label []
-property_value: DiffAvg "322.17" xsd:float
-property_value: DiffFormula "C 9 H 11 N 2 O 9 P 1" xsd:string
-property_value: DiffMono "322.020217" xsd:float
-property_value: Formula "C 20 H 21 N 4 O 10 P 1" xsd:string
-property_value: MassAvg "508.38" xsd:float
-property_value: MassMono "508.099530" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:292
-is_a: MOD:00611
-is_a: MOD:00918
-
-[Term]
-id: MOD:01250
-name: iodouridine monophosphate derivatized phenylalanine
-def: "A protein modification that is produced by reaction of iodouridine monophosphate with an L-phenylalanine residue." [PubMed:11112526, PubMed:11567090, PubMed:6540775, Unimod:292#F]
-comment: This has a carbon-carbon linkage and not a phosphodiester linkage with UMP.
-synonym: "Cross-link of (Iodo)-uracil MP with W,F,Y" RELATED Unimod-description []
-synonym: "IodoU-AMP" RELATED PSI-MS-label []
-property_value: DiffAvg "322.17" xsd:float
-property_value: DiffFormula "C 9 H 11 N 2 O 9 P 1" xsd:string
-property_value: DiffMono "322.020217" xsd:float
-property_value: Formula "C 18 H 20 N 3 O 10 P 1" xsd:string
-property_value: MassAvg "469.34" xsd:float
-property_value: MassMono "469.088630" xsd:float
-property_value: Origin "F" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:292
-is_a: MOD:00611
-is_a: MOD:00914
-
-[Term]
-id: MOD:01251
-name: N6-[3-(carboxamidomethylthio)propanoyl]lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-[3-(carboxamidomethylthio)propanoyl]lysine." [PubMed:15121203, Unimod:293#K]
-synonym: "3-(carbamidomethylthio)propanoyl" RELATED Unimod-description []
-synonym: "CAMthiopropanoyl" RELATED PSI-MS-label []
-property_value: DiffAvg "145.18" xsd:float
-property_value: DiffFormula "C 5 H 7 N 1 O 2 S 1" xsd:string
-property_value: DiffMono "145.019749" xsd:float
-property_value: Formula "C 11 H 19 N 3 O 3 S 1" xsd:string
-property_value: MassAvg "273.35" xsd:float
-property_value: MassMono "273.114712" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:293
-is_a: MOD:00612
-is_a: MOD:01875
-
-[Term]
-id: MOD:01252
-name: 5-hydro-5-methylimidazol-4-one, methylglyoxal arginine adduct (+54 amu)
-def: "OBSOLETE because redundant and identical to MOD:00933. Remap to MOD:00933." [PubMed:9448752, Unimod:319#R]
-synonym: "Delta:H(2)C(3)O(1)" RELATED PSI-MS-label []
-synonym: "MDA adduct +54" RELATED Unimod-description []
-property_value: DiffAvg "54.05" xsd:float
-property_value: DiffFormula "C 3 H 2 O 1" xsd:string
-property_value: DiffMono "54.010565" xsd:float
-property_value: Formula "C 9 H 14 N 4 O 2" xsd:string
-property_value: MassAvg "210.24" xsd:float
-property_value: MassMono "210.111676" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "artifact" xsd:string
-replaced_by: MOD:00933
-xref: Unimod:319
-is_obsolete: true
-
-[Term]
-id: MOD:01253
-name: malondialdehyde lysine adduct (+54 amu)
-def: "modification from Unimod Chemical derivative - Malondialdehyde (MDA) adduct" [Unimod:319#K]
-synonym: "Delta:H(2)C(3)O(1)" RELATED PSI-MS-label []
-synonym: "MDA adduct +54" RELATED Unimod-description []
-property_value: DiffAvg "54.05" xsd:float
-property_value: DiffFormula "C 3 H 2 O 1" xsd:string
-property_value: DiffMono "54.010565" xsd:float
-property_value: Formula "C 9 H 14 N 2 O 2" xsd:string
-property_value: MassAvg "182.22" xsd:float
-property_value: MassMono "182.105528" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:319
-is_a: MOD:00630
-is_a: MOD:00912
-
-[Term]
-id: MOD:01254
-name: 4x(2)H labeled dimethylated L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to 4x(2)H labeled dimethylated L-lysine." [OMSSA:189, PubMed:14670044, Unimod:199#K]
-subset: PSI-MOD-slim
-synonym: "DiMethyl-CHD2" RELATED Unimod-description []
-synonym: "Dimethyl:2H(4)" RELATED PSI-MS-label []
-synonym: "mod189" EXACT OMSSA-label []
-property_value: DiffAvg "32.06" xsd:float
-property_value: DiffFormula "C 2 (2)H 4" xsd:string
-property_value: DiffMono "32.056407" xsd:float
-property_value: Formula "C 8 H 12 (2)H 4 N 2 O 1" xsd:string
-property_value: MassAvg "160.15" xsd:float
-property_value: MassMono "160.151370" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:199
-is_a: MOD:00552
-is_a: MOD:00912
-relationship: derives_from MOD:00084
-
-[Term]
-id: MOD:01255
-name: S-(2-sulfanylethyl)cysteine (Ser)
-def: "A protein modification that effectively converts an L-serine residue to S-(2-sulfanylethyl)cysteine." [PubMed:11507762, Unimod:200#S]
-synonym: "EDT" RELATED Unimod-description []
-synonym: "Ethanedithiol" RELATED PSI-MS-label []
-synonym: "S-(2-mercaptoethyl)cysteine" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "76.18" xsd:float
-property_value: DiffFormula "C 2 H 4 O -1 S 2" xsd:string
-property_value: DiffMono "75.980528" xsd:float
-property_value: Formula "C 5 H 9 N 1 O 1 S 2" xsd:string
-property_value: MassAvg "163.25" xsd:float
-property_value: MassMono "163.012556" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:200
-is_a: MOD:00553
-is_a: MOD:00916
-
-[Term]
-id: MOD:01256
-name: 3-methyl-S-(2-sulfanylethyl)cysteine (Thr)
-def: "A protein modification that effectively converts an L-threonine residue to 3-methyl-S-(2-sulfanylethyl)cysteine." [PubMed:11507762, Unimod:200#T]
-synonym: "beta-methyl-S-(2-mercaptoethyl)cysteine" EXACT PSI-MOD-alternate []
-synonym: "EDT" RELATED Unimod-description []
-synonym: "Ethanedithiol" RELATED PSI-MS-label []
-property_value: DiffAvg "76.18" xsd:float
-property_value: DiffFormula "C 2 H 4 O -1 S 2" xsd:string
-property_value: DiffMono "75.980528" xsd:float
-property_value: Formula "C 6 H 11 N 1 O 1 S 2" xsd:string
-property_value: MassAvg "177.28" xsd:float
-property_value: MassMono "177.028206" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:200
-is_a: MOD:00553
-is_a: MOD:00917
-
-[Term]
-id: MOD:01257
-name: 6-aminoquinolyl-N-hydroxysuccinimidyl carbamate - site K
-def: "modification from Unimod Chemical derivative -" [PubMed:12716131, PubMed:14997490, Unimod:194#K]
-synonym: "6-aminoquinolyl-N-hydroxysuccinimidyl carbamate" RELATED Unimod-description []
-synonym: "AccQTag" RELATED PSI-MS-label []
-property_value: DiffAvg "170.17" xsd:float
-property_value: DiffFormula "C 10 H 6 N 2 O 1" xsd:string
-property_value: DiffMono "170.048013" xsd:float
-property_value: Formula "C 16 H 18 N 4 O 2" xsd:string
-property_value: MassAvg "298.35" xsd:float
-property_value: MassMono "298.142976" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:194
-is_a: MOD:00547
-
-[Term]
-id: MOD:01258
-name: N-methylmaleimide modified L-cysteine
-def: "modification from Unimod Chemical derivative -" [PubMed:9448752, Unimod:314#C]
-synonym: "Nmethylmaleimide" RELATED PSI-MS-label []
-synonym: "Nmethylmaleimide" RELATED Unimod-description []
-property_value: DiffAvg "111.10" xsd:float
-property_value: DiffFormula "C 5 H 5 N 1 O 2" xsd:string
-property_value: DiffMono "111.032028" xsd:float
-property_value: Formula "C 8 H 10 N 2 O 3 S 1" xsd:string
-property_value: MassAvg "214.24" xsd:float
-property_value: MassMono "214.041213" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:314
-is_a: MOD:00625
-is_a: MOD:00905
-
-[Term]
-id: MOD:01259
-name: N-methylmaleimide modified L-lysine
-def: "modification from Unimod Chemical derivative -" [PubMed:9448752, Unimod:314#K]
-synonym: "Nmethylmaleimide" RELATED PSI-MS-label []
-synonym: "Nmethylmaleimide" RELATED Unimod-description []
-property_value: DiffAvg "111.10" xsd:float
-property_value: DiffFormula "C 5 H 5 N 1 O 2" xsd:string
-property_value: DiffMono "111.032028" xsd:float
-property_value: Formula "C 11 H 17 N 3 O 3" xsd:string
-property_value: MassAvg "239.27" xsd:float
-property_value: MassMono "239.126991" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:314
-is_a: MOD:00625
-is_a: MOD:00912
-
-[Term]
-id: MOD:01260
-name: nucleophilic addtion to cytopiloyne - site Y
-def: "OBSOLETE because there is no evidence in the literature of covalent modification of polypeptides with cytopiloyne or cytopiloyne+H2O.  Modifications could potentially happen, but are not experimentally verified. [PMT] modification from Unimod Chemical derivative -" [PubMed:15549660, Unimod:270#Y]
-synonym: "Cytopiloyne" RELATED PSI-MS-label []
-synonym: "nucleophilic addtion to cytopiloyne" RELATED Unimod-description []
-property_value: DiffAvg "362.38" xsd:float
-property_value: DiffFormula "C 19 H 22 O 7" xsd:string
-property_value: DiffMono "362.136553" xsd:float
-property_value: Formula "C 28 H 31 N 1 O 9" xsd:string
-property_value: MassAvg "525.55" xsd:float
-property_value: MassMono "525.199882" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:270
-is_obsolete: true
-
-[Term]
-id: MOD:01261
-name: nucleophilic addtion to cytopiloyne - site S
-def: "OBSOLETE because there is no evidence in the literature of covalent modification of polypeptides with cytopiloyne or cytopiloyne+H2O.  Modifications could potentially happen, but are not experimentally verified. [PMT] modification from Unimod Chemical derivative -" [PubMed:15549660, Unimod:270#C]
-synonym: "Cytopiloyne" RELATED PSI-MS-label []
-synonym: "nucleophilic addtion to cytopiloyne" RELATED Unimod-description []
-property_value: DiffAvg "362.38" xsd:float
-property_value: DiffFormula "C 19 H 22 O 7" xsd:string
-property_value: DiffMono "362.136553" xsd:float
-property_value: Formula "C 22 H 27 N 1 O 9" xsd:string
-property_value: MassAvg "449.46" xsd:float
-property_value: MassMono "449.168581" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:270
-is_obsolete: true
-
-[Term]
-id: MOD:01262
-name: nucleophilic addition to cytopiloyne - site R
-def: "OBSOLETE because there is no evidence in the literature of covalent modification of polypeptides with cytopiloyne or cytopiloyne+H2O.  Modifications could potentially happen, but are not experimentally verified. [PMT] modification from Unimod Chemical derivative -" [PubMed:12590383, PubMed:15549660, Unimod:270#R]
-synonym: "Cytopiloyne" RELATED PSI-MS-label []
-synonym: "nucleophilic addtion to cytopiloyne" RELATED Unimod-description []
-property_value: DiffAvg "362.38" xsd:float
-property_value: DiffFormula "C 19 H 22 O 7" xsd:string
-property_value: DiffMono "362.136553" xsd:float
-property_value: Formula "C 25 H 34 N 4 O 8" xsd:string
-property_value: MassAvg "518.57" xsd:float
-property_value: MassMono "518.237664" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:270
-is_obsolete: true
-
-[Term]
-id: MOD:01263
-name: nucleophilic addtion to cytopiloyne - site K
-def: "OBSOLETE because there is no evidence in the literature of covalent modification of polypeptides with cytopiloyne or cytopiloyne+H2O.  Modifications could potentially happen, but are not experimentally verified. [PMT] modification from Unimod Chemical derivative -" [PubMed:15549660, Unimod:270#K]
-synonym: "Cytopiloyne" RELATED PSI-MS-label []
-synonym: "nucleophilic addtion to cytopiloyne" RELATED Unimod-description []
-property_value: DiffAvg "362.38" xsd:float
-property_value: DiffFormula "C 19 H 22 O 7" xsd:string
-property_value: DiffMono "362.136553" xsd:float
-property_value: Formula "C 25 H 34 N 2 O 8" xsd:string
-property_value: MassAvg "490.55" xsd:float
-property_value: MassMono "490.231516" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:270
-is_obsolete: true
-
-[Term]
-id: MOD:01264
-name: nucleophilic addtion to cytopiloyne - site C
-def: "OBSOLETE because there is no evidence in the literature of covalent modification of polypeptides with cytopiloyne or cytopiloyne+H2O.  Modifications could potentially happen, but are not experimentally verified. [PMT] modification from Unimod Chemical derivative -" [PubMed:15549660, Unimod:270#C]
-synonym: "Cytopiloyne" RELATED PSI-MS-label []
-synonym: "nucleophilic addtion to cytopiloyne" RELATED Unimod-description []
-property_value: DiffAvg "362.38" xsd:float
-property_value: DiffFormula "C 19 H 22 O 7" xsd:string
-property_value: DiffMono "362.136553" xsd:float
-property_value: Formula "C 22 H 27 N 1 O 8 S 1" xsd:string
-property_value: MassAvg "465.52" xsd:float
-property_value: MassMono "465.145738" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:270
-is_obsolete: true
-
-[Term]
-id: MOD:01265
-name: nucleophilic addtion to cytopiloyne - site P
-def: "OBSOLETE because there is no evidence in the literature of covalent modification of polypeptides with cytopiloyne or cytopiloyne+H2O.  Modifications could potentially happen, but are not experimentally verified. [PMT] modification from Unimod Chemical derivative -" [PubMed:15549660, Unimod:270#P]
-synonym: "Cytopiloyne" RELATED PSI-MS-label []
-synonym: "nucleophilic addtion to cytopiloyne" RELATED Unimod-description []
-property_value: DiffAvg "362.38" xsd:float
-property_value: DiffFormula "C 19 H 22 O 7" xsd:string
-property_value: DiffMono "362.136553" xsd:float
-property_value: Formula "C 24 H 29 N 1 O 8" xsd:string
-property_value: MassAvg "459.50" xsd:float
-property_value: MassMono "459.189317" xsd:float
-property_value: Origin "P" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:270
-is_obsolete: true
-
-[Term]
-id: MOD:01266
-name: nucleophilic addition to cytopiloyne+H2O - site C
-def: "OBSOLETE because there is no evidence in the literature of covalent modification of polypeptides with cytopiloyne or cytopiloyne+H2O.  Modifications could potentially happen, but are not experimentally verified. [PMT] modification from Unimod Chemical derivative -" [PubMed:15549660, Unimod:271#C]
-synonym: "Cytopiloyne+water" RELATED PSI-MS-label []
-synonym: "nucleophilic addition to cytopiloyne+H2O" RELATED Unimod-description []
-property_value: DiffAvg "380.39" xsd:float
-property_value: DiffFormula "C 19 H 24 O 8" xsd:string
-property_value: DiffMono "380.147118" xsd:float
-property_value: Formula "C 22 H 29 N 1 O 9 S 1" xsd:string
-property_value: MassAvg "483.53" xsd:float
-property_value: MassMono "483.156303" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:271
-is_obsolete: true
-
-[Term]
-id: MOD:01267
-name: nucleophilic addition to cytopiloyne+H2O - site K
-def: "OBSOLETE because there is no evidence in the literature of covalent modification of polypeptides with cytopiloyne or cytopiloyne+H2O.  Modifications could potentially happen, but are not experimentally verified. [PMT] modification from Unimod Chemical derivative -" [PubMed:11746907, PubMed:15549660, Unimod:271#K]
-synonym: "Cytopiloyne+water" RELATED PSI-MS-label []
-synonym: "nucleophilic addition to cytopiloyne+H2O" RELATED Unimod-description []
-property_value: DiffAvg "380.39" xsd:float
-property_value: DiffFormula "C 19 H 24 O 8" xsd:string
-property_value: DiffMono "380.147118" xsd:float
-property_value: Formula "C 25 H 36 N 2 O 9" xsd:string
-property_value: MassAvg "508.57" xsd:float
-property_value: MassMono "508.242081" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:271
-is_obsolete: true
-
-[Term]
-id: MOD:01268
-name: nucleophilic addition to cytopiloyne+H2O - site T
-def: "OBSOLETE because there is no evidence in the literature of covalent modification of polypeptides with cytopiloyne or cytopiloyne+H2O.  Modifications could potentially happen, but are not experimentally verified. [PMT] modification from Unimod Chemical derivative -" [PubMed:15549660, Unimod:271#T]
-synonym: "Cytopiloyne+water" RELATED PSI-MS-label []
-synonym: "nucleophilic addition to cytopiloyne+H2O" RELATED Unimod-description []
-property_value: DiffAvg "380.39" xsd:float
-property_value: DiffFormula "C 19 H 24 O 8" xsd:string
-property_value: DiffMono "380.147118" xsd:float
-property_value: Formula "C 23 H 31 N 1 O 10" xsd:string
-property_value: MassAvg "481.50" xsd:float
-property_value: MassMono "481.194796" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:271
-is_obsolete: true
-
-[Term]
-id: MOD:01269
-name: nucleophilic addition to cytopiloyne+H2O - site R
-def: "OBSOLETE because there is no evidence in the literature of covalent modification of polypeptides with cytopiloyne or cytopiloyne+H2O.  Modifications could potentially happen, but are not experimentally verified. [PMT] modification from Unimod Chemical derivative -" [PubMed:15549660, Unimod:271#R]
-synonym: "Cytopiloyne+water" RELATED PSI-MS-label []
-synonym: "nucleophilic addition to cytopiloyne+H2O" RELATED Unimod-description []
-property_value: DiffAvg "380.39" xsd:float
-property_value: DiffFormula "C 19 H 24 O 8" xsd:string
-property_value: DiffMono "380.147118" xsd:float
-property_value: Formula "C 25 H 36 N 4 O 9" xsd:string
-property_value: MassAvg "536.58" xsd:float
-property_value: MassMono "536.248229" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:271
-is_obsolete: true
-
-[Term]
-id: MOD:01270
-name: nucleophilic addition to cytopiloyne+H2O - site S
-def: "OBSOLETE because there is no evidence in the literature of covalent modification of polypeptides with cytopiloyne or cytopiloyne+H2O.  Modifications could potentially happen, but are not experimentally verified. [PMT] modification from Unimod Chemical derivative -" [PubMed:14670044, PubMed:15549660, Unimod:271#S]
-synonym: "Cytopiloyne+water" RELATED PSI-MS-label []
-synonym: "nucleophilic addition to cytopiloyne+H2O" RELATED Unimod-description []
-property_value: DiffAvg "380.39" xsd:float
-property_value: DiffFormula "C 19 H 24 O 8" xsd:string
-property_value: DiffMono "380.147118" xsd:float
-property_value: Formula "C 22 H 29 N 1 O 10" xsd:string
-property_value: MassAvg "467.47" xsd:float
-property_value: MassMono "467.179146" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:271
-is_obsolete: true
-
-[Term]
-id: MOD:01271
-name: nucleophilic addition to cytopiloyne+H2O - site Y
-def: "OBSOLETE because there is no evidence in the literature of covalent modification of polypeptides with cytopiloyne or cytopiloyne+H2O.  Modifications could potentially happen, but are not experimentally verified. [PMT] modification from Unimod Chemical derivative -" [PubMed:15549660, Unimod:271#Y]
-synonym: "Cytopiloyne+water" RELATED PSI-MS-label []
-synonym: "nucleophilic addition to cytopiloyne+H2O" RELATED Unimod-description []
-property_value: DiffAvg "380.39" xsd:float
-property_value: DiffFormula "C 19 H 24 O 8" xsd:string
-property_value: DiffMono "380.147118" xsd:float
-property_value: Formula "C 28 H 33 N 1 O 10" xsd:string
-property_value: MassAvg "543.57" xsd:float
-property_value: MassMono "543.210446" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:271
-is_obsolete: true
-
-[Term]
-id: MOD:01272
-name: iminobiotinylation - site K
-def: "modification from Unimod Chemical derivative -" [PubMed:9750125, Unimod:89#K]
-synonym: "Iminobiotin" RELATED PSI-MS-label []
-synonym: "Iminobiotinylation" RELATED Unimod-description []
-property_value: DiffAvg "225.31" xsd:float
-property_value: DiffFormula "C 10 H 15 N 3 O 1 S 1" xsd:string
-property_value: DiffMono "225.093583" xsd:float
-property_value: Formula "C 16 H 27 N 5 O 2 S 1" xsd:string
-property_value: MassAvg "353.49" xsd:float
-property_value: MassMono "353.188546" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:89
-is_a: MOD:00467
-is_a: MOD:01875
-
-[Term]
-id: MOD:01273
-name: O-[4-(2-aminoethyl)benzenesulfonyl] serine
-def: "A protein modification that is produced by formation of an adduct with 4-(2-aminoethyl)benzenesulfonyl fluoride, AEBS, and an L-serine residue." [PubMed:15283597, PubMed:8597590, Unimod:276#S]
-synonym: "AEBS" RELATED PSI-MS-label []
-synonym: "Aminoethylbenzenesulfonylation" RELATED Unimod-description []
-property_value: DiffAvg "183.23" xsd:float
-property_value: DiffFormula "C 8 H 9 N 1 O 2 S 1" xsd:string
-property_value: DiffMono "183.035400" xsd:float
-property_value: Formula "C 11 H 14 N 2 O 4 S 1" xsd:string
-property_value: MassAvg "270.30" xsd:float
-property_value: MassMono "270.067428" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:276
-is_a: MOD:00596
-is_a: MOD:00916
-
-[Term]
-id: MOD:01274
-name: N'-[4-(2-aminoethyl)benzenesulfonyl] derivatized histidine
-def: "A protein modification that is produced by formation of an adduct with 4-(2-aminoethyl)benzenesulfonyl fluoride, AEBS, and an L-histidine residue." [PubMed:8597590, Unimod:276#H]
-synonym: "AEBS" RELATED PSI-MS-label []
-synonym: "Aminoethylbenzenesulfonylation" RELATED Unimod-description []
-property_value: DiffAvg "183.23" xsd:float
-property_value: DiffFormula "C 8 H 9 N 1 O 2 S 1" xsd:string
-property_value: DiffMono "183.035400" xsd:float
-property_value: Formula "C 14 H 16 N 4 O 3 S 1" xsd:string
-property_value: MassAvg "320.37" xsd:float
-property_value: MassMono "320.094311" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:276
-is_a: MOD:00596
-is_a: MOD:00909
-
-[Term]
-id: MOD:01275
-name: N6-[4-(2-aminoethyl)benzenesulfonyl]lysine
-def: "A protein modification that is produced by formation of an adduct with 4-(2-aminoethyl)benzenesulfonyl fluoride, AEBS, and an L-lysine residue." [PubMed:8597590, Unimod:276#K]
-synonym: "AEBS" RELATED PSI-MS-label []
-synonym: "Aminoethylbenzenesulfonylation" RELATED Unimod-description []
-property_value: DiffAvg "183.23" xsd:float
-property_value: DiffFormula "C 8 H 9 N 1 O 2 S 1" xsd:string
-property_value: DiffMono "183.035400" xsd:float
-property_value: Formula "C 14 H 21 N 3 O 3 S 1" xsd:string
-property_value: MassAvg "311.40" xsd:float
-property_value: MassMono "311.130363" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:276
-is_a: MOD:00596
-is_a: MOD:00912
-
-[Term]
-id: MOD:01276
-name: O4'-[4-(2-aminoethyl)benzenesulfonyl]tyrosine
-def: "A protein modification that is produced by formation of an adduct with 4-(2-aminoethyl)benzenesulfonyl fluoride, AEBS, and an L-tyrosine residue." [PubMed:10906242, PubMed:8597590, Unimod:276#Y]
-synonym: "AEBS" RELATED PSI-MS-label []
-synonym: "Aminoethylbenzenesulfonylation" RELATED Unimod-description []
-property_value: DiffAvg "183.23" xsd:float
-property_value: DiffFormula "C 8 H 9 N 1 O 2 S 1" xsd:string
-property_value: DiffMono "183.035400" xsd:float
-property_value: Formula "C 17 H 18 N 2 O 4 S 1" xsd:string
-property_value: MassAvg "346.40" xsd:float
-property_value: MassMono "346.098728" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:276
-is_a: MOD:00596
-is_a: MOD:00919
-
-[Term]
-id: MOD:01277
-name: crotonylated L-cysteine
-def: "modification from Unimod Other -" [PubMed:11283024, Unimod:253#C]
-synonym: "Crotonaldehyde" RELATED PSI-MS-label []
-synonym: "Crotonaldehyde" RELATED Unimod-description []
-property_value: DiffAvg "70.09" xsd:float
-property_value: DiffFormula "C 4 H 6 O 1" xsd:string
-property_value: DiffMono "70.041865" xsd:float
-property_value: Formula "C 7 H 11 N 1 O 2 S 1" xsd:string
-property_value: MassAvg "173.23" xsd:float
-property_value: MassMono "173.051050" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:253
-is_a: MOD:00576
-is_a: MOD:00905
-
-[Term]
-id: MOD:01278
-name: crotonylated L-lysine
-def: "modification from Unimod Other -" [PubMed:11283024, Unimod:253#K]
-synonym: "Crotonaldehyde" RELATED PSI-MS-label []
-synonym: "Crotonaldehyde" RELATED Unimod-description []
-property_value: DiffAvg "70.09" xsd:float
-property_value: DiffFormula "C 4 H 6 O 1" xsd:string
-property_value: DiffMono "70.041865" xsd:float
-property_value: Formula "C 10 H 18 N 2 O 2" xsd:string
-property_value: MassAvg "198.27" xsd:float
-property_value: MassMono "198.136828" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:253
-is_a: MOD:00576
-is_a: MOD:00912
-
-[Term]
-id: MOD:01279
-name: crotonylated L-histidine
-def: "modification from Unimod Other -" [PubMed:11283024, PubMed:1443554, Unimod:253#H]
-synonym: "Crotonaldehyde" RELATED PSI-MS-label []
-synonym: "Crotonaldehyde" RELATED Unimod-description []
-property_value: DiffAvg "70.09" xsd:float
-property_value: DiffFormula "C 4 H 6 O 1" xsd:string
-property_value: DiffMono "70.041865" xsd:float
-property_value: Formula "C 10 H 13 N 3 O 2" xsd:string
-property_value: MassAvg "207.23" xsd:float
-property_value: MassMono "207.100777" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:253
-is_a: MOD:00576
-is_a: MOD:00909
-
-[Term]
-id: MOD:01280
-name: EDT-iodo-PEO-biotin - site T
-def: "modification from Unimod Chemical derivative -" [PubMed:11857757, PubMed:12175151, Unimod:118#T]
-synonym: "EDT-iodo-PEO-biotin" RELATED Unimod-description []
-synonym: "EDT-iodoacetyl-PEO-biotin" RELATED PSI-MS-label []
-property_value: DiffAvg "490.70" xsd:float
-property_value: DiffFormula "C 20 H 34 N 4 O 4 S 3" xsd:string
-property_value: DiffMono "490.174219" xsd:float
-property_value: Formula "C 24 H 41 N 5 O 6 S 3" xsd:string
-property_value: MassAvg "591.80" xsd:float
-property_value: MassMono "591.221897" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:118
-is_a: MOD:00490
-is_a: MOD:00917
-
-[Term]
-id: MOD:01281
-name: EDT-iodo-PEO-biotin - site S
-def: "modification from Unimod Chemical derivative -" [PubMed:16335955, Unimod:118#S]
-synonym: "EDT-iodo-PEO-biotin" RELATED Unimod-description []
-synonym: "EDT-iodoacetyl-PEO-biotin" RELATED PSI-MS-label []
-property_value: DiffAvg "490.70" xsd:float
-property_value: DiffFormula "C 20 H 34 N 4 O 4 S 3" xsd:string
-property_value: DiffMono "490.174219" xsd:float
-property_value: Formula "C 23 H 39 N 5 O 6 S 3" xsd:string
-property_value: MassAvg "577.77" xsd:float
-property_value: MassMono "577.206247" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:118
-is_a: MOD:00490
-is_a: MOD:00916
-
-[Term]
-id: MOD:01282
-name: acrolein addition +56 - site H
-def: "OBSOLETE because this modification is not supported by the linked literature [PMT]" [PubMed:10825247, PubMed:15541752, Unimod:206#H]
-synonym: "Acrolein addition +56" RELATED Unimod-description []
-synonym: "Delta:H(4)C(3)O(1)" RELATED PSI-MS-label []
-property_value: DiffAvg "56.06" xsd:float
-property_value: DiffFormula "C 3 H 4 O 1" xsd:string
-property_value: DiffMono "56.026215" xsd:float
-property_value: Formula "C 9 H 11 N 3 O 2" xsd:string
-property_value: MassAvg "193.21" xsd:float
-property_value: MassMono "193.085127" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:206
-is_obsolete: true
-
-[Term]
-id: MOD:01283
-name: acrolein addition +56 - site K
-def: "OBSOLETE because this modification is not supported by the linked literature [PMT]" [PubMed:10825247, PubMed:15541752, Unimod:206#K]
-synonym: "Acrolein addition +56" RELATED Unimod-description []
-synonym: "Delta:H(4)C(3)O(1)" RELATED PSI-MS-label []
-property_value: DiffAvg "56.06" xsd:float
-property_value: DiffFormula "C 3 H 4 O 1" xsd:string
-property_value: DiffMono "56.026215" xsd:float
-property_value: Formula "C 9 H 16 N 2 O 2" xsd:string
-property_value: MassAvg "184.24" xsd:float
-property_value: MassMono "184.121178" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:206
-is_obsolete: true
-
-[Term]
-id: MOD:01284
-name: acrolein addition +56 - site C
-def: "OBSOLETE because this modification is not supported by the linked literature [PMT]" [PubMed:10825247, PubMed:15541752, PubMed:9254591, Unimod:206#C]
-synonym: "Acrolein addition +56" RELATED Unimod-description []
-synonym: "Delta:H(4)C(3)O(1)" RELATED PSI-MS-label []
-property_value: DiffAvg "56.06" xsd:float
-property_value: DiffFormula "C 3 H 4 O 1" xsd:string
-property_value: DiffMono "56.026215" xsd:float
-property_value: Formula "C 6 H 9 N 1 O 2 S 1" xsd:string
-property_value: MassAvg "159.20" xsd:float
-property_value: MassMono "159.035400" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:206
-is_obsolete: true
-
-[Term]
-id: MOD:01285
-name: 6x(13)C,1x(15)N labeled L-leucine
-def: "A protein modification that effectively converts an L-leucine residue to 6x(13)C,1x(15)N isotope labeled L-leucine." [PubMed:11857757, PubMed:11999733, PubMed:12175151, Unimod:695#L]
-synonym: "13C(6) 15N(1) Silac label" RELATED Unimod-description []
-synonym: "Label:13C(6)15N(1)" RELATED PSI-MS-label []
-property_value: DiffAvg "7.02" xsd:float
-property_value: DiffFormula "(12)C -6 (13)C 6 (14)N -1 (15)N 1" xsd:string
-property_value: DiffMono "7.017164" xsd:float
-property_value: Formula "(13)C 6 H 11 (15)N 1 O 1" xsd:string
-property_value: MassAvg "120.10" xsd:float
-property_value: MassMono "120.101228" xsd:float
-property_value: Origin "L" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:695
-is_a: MOD:00911
-is_a: MOD:01370
-
-[Term]
-id: MOD:01286
-name: 6x(13)C,1x(15)N labeled L-isoleucine
-def: "A protein modification that effectively converts an L-isoleucine residue to 6x(13)C,1x(15)N isotope labeled L-isoleucine." [PubMed:11857757, PubMed:11999733, PubMed:12175151, Unimod:695#I]
-synonym: "13C(6) 15N(1) Silac label" RELATED Unimod-description []
-synonym: "Label:13C(6)15N(1)" RELATED PSI-MS-label []
-property_value: DiffAvg "7.02" xsd:float
-property_value: DiffFormula "(12)C -6 (13)C 6 (14)N -1 (15)N 1" xsd:string
-property_value: DiffMono "7.017164" xsd:float
-property_value: Formula "(13)C 6 H 11 (15)N 1 O 1" xsd:string
-property_value: MassAvg "120.10" xsd:float
-property_value: MassMono "120.101228" xsd:float
-property_value: Origin "I" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:695
-is_a: MOD:00910
-is_a: MOD:01370
-
-[Term]
-id: MOD:01287
-name: Bruker Daltonics SERVA-ICPL(TM) quantification chemistry, heavy form - site K
-def: "modification from Unimod Isotopic label -" [PubMed:11857757, PubMed:15602776, Unimod:364#K]
-synonym: "Bruker Daltonics SERVA-ICPL(TM) quantification chemistry, heavy form" RELATED Unimod-description []
-synonym: "ICPL:13C(6)" RELATED PSI-MS-label []
-property_value: DiffAvg "111.04" xsd:float
-property_value: DiffFormula "(13)C 6 H 3 N 1 O 1" xsd:string
-property_value: DiffMono "111.041593" xsd:float
-property_value: Formula "C 6 (13)C 6 H 15 N 3 O 2" xsd:string
-property_value: MassAvg "239.14" xsd:float
-property_value: MassMono "239.136556" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:364
-is_a: MOD:00789
-is_a: MOD:00912
-
-[Term]
-id: MOD:01288
-name: acetaldehyde +28 - site H
-def: "OBSOLETE because this is not supported by the literature [PMT]" [Unimod:255#H]
-synonym: "Acetaldehyde +28" RELATED Unimod-description []
-synonym: "Delta:H(4)C(2)" RELATED PSI-MS-label []
-property_value: DiffAvg "28.05" xsd:float
-property_value: DiffFormula "C 2 H 4" xsd:string
-property_value: DiffMono "28.031300" xsd:float
-property_value: Formula "C 8 H 11 N 3 O 1" xsd:string
-property_value: MassAvg "165.20" xsd:float
-property_value: MassMono "165.090212" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:255
-is_obsolete: true
-
-[Term]
-id: MOD:01289
-name: acetaldehyde +28 - site K
-def: "OBSOLETE because this is not supported by the literature [PMT]" [Unimod:255#K]
-synonym: "Acetaldehyde +28" RELATED Unimod-description []
-synonym: "Delta:H(4)C(2)" RELATED PSI-MS-label []
-property_value: DiffAvg "28.05" xsd:float
-property_value: DiffFormula "C 2 H 4" xsd:string
-property_value: DiffMono "28.031300" xsd:float
-property_value: Formula "C 8 H 16 N 2 O 1" xsd:string
-property_value: MassAvg "156.23" xsd:float
-property_value: MassMono "156.126263" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:255
-is_obsolete: true
-
-[Term]
-id: MOD:01290
-name: dihydroxylated residue - site F
-def: "OBSOLETE because redundant and identical to MOD:00465. Remap to MOD:00465." [PubMed:11857757, PubMed:12175151, PubMed:12686488, PubMed:9252331, Unimod:425]
-synonym: "dihydroxy" RELATED Unimod-description []
-synonym: "Dioxidation" RELATED PSI-MS-label []
-property_value: DiffAvg "32.00" xsd:float
-property_value: DiffFormula "O 2" xsd:string
-property_value: DiffMono "31.989829" xsd:float
-property_value: Formula "C 9 H 9 N 1 O 3" xsd:string
-property_value: MassAvg "179.17" xsd:float
-property_value: MassMono "179.058243" xsd:float
-property_value: Origin "F" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:425
-replaced_by: MOD:00465
-is_obsolete: true
-
-[Term]
-id: MOD:01291
-name: dihydroxylated residue - site W
-def: "OBSOLETE because redundant and identical to MOD:00464. Remap to MOD:00464." [PubMed:12643539, PubMed:12686488, PubMed:6273432, PubMed:9252331, Unimod:425]
-synonym: "dihydroxy" RELATED Unimod-description []
-synonym: "Dioxidation" RELATED PSI-MS-label []
-property_value: DiffAvg "32.00" xsd:float
-property_value: DiffFormula "O 2" xsd:string
-property_value: DiffMono "31.989829" xsd:float
-property_value: Formula "C 11 H 10 N 2 O 3" xsd:string
-property_value: MassAvg "218.21" xsd:float
-property_value: MassMono "218.069142" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "artifact" xsd:string
-replaced_by: MOD:00464
-xref: Unimod:425
-is_obsolete: true
-
-[Term]
-id: MOD:01292
-name: dimethylation of proline residue
-def: "OBSOLETE because redundant and identical to MOD:00075. Map to MOD:00075." [Unimod:529]
-synonym: "Delta:H(5)C(2)" RELATED PSI-MS-label []
-synonym: "Dimethylation of proline residue" RELATED Unimod-description []
-property_value: DiffAvg "29.06" xsd:float
-property_value: DiffFormula "C 2 H 5" xsd:string
-property_value: DiffMono "29.039125" xsd:float
-property_value: Origin "P" xsd:string
-property_value: Source "natural" xsd:string
-replaced_by: MOD:00075
-xref: Unimod:529
-is_obsolete: true
-
-[Term]
-id: MOD:01293
-name: 1x(18)O labeled deamidated L-asparagine
-def: "A protein modification that effectively converts an L-asparagine residue to L-aspartic acid with one (18)O." [OMSSA:139, PubMed:8382902, Unimod:366#N]
-subset: PSI-MOD-slim
-synonym: "Deamidated:18O(1)" RELATED PSI-MS-label []
-synonym: "Deamidation in presence of O18" RELATED Unimod-description []
-synonym: "oxy18" EXACT OMSSA-label []
-property_value: DiffAvg "2.99" xsd:float
-property_value: DiffFormula "H -1 N -1 (18)O 1" xsd:string
-property_value: DiffMono "2.988262" xsd:float
-property_value: Formula "C 4 H 5 N 1 (16)O 2 (18)O 1" xsd:string
-property_value: MassAvg "117.03" xsd:float
-property_value: MassMono "117.031189" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:366
-is_a: MOD:00852
-relationship: derives_from MOD:00684
-
-[Term]
-id: MOD:01294
-name: deamidation in presence of O18 -site Q
-def: "OBSOLETE identical and redundant with MOD:00791. Remap to MOD:00791." [PubMed:8382902]
-synonym: "Deamidated:18O(1)" RELATED PSI-MS-label []
-synonym: "Deamidation in presence of O18" RELATED Unimod-description []
-property_value: DiffAvg "2.99" xsd:float
-property_value: DiffFormula "H -1 N -1 (18)O 1" xsd:string
-property_value: DiffMono "2.988262" xsd:float
-property_value: Origin "Q" xsd:string
-property_value: Source "artifact" xsd:string
-replaced_by: MOD:00791
-is_obsolete: true
-
-[Term]
-id: MOD:01295
-name: monosodium L-aspartate
-def: "A protein modification that effectively converts an L-aspartic acid residue to monosodium L-aspartate." [PubMed:12216740, Unimod:30#D]
-subset: PSI-MOD-slim
-synonym: "Cation:Na" RELATED PSI-MS-label []
-synonym: "Na1Asp" EXACT PSI-MOD-label []
-synonym: "Sodium adduct" RELATED Unimod-description []
-property_value: DiffAvg "21.98" xsd:float
-property_value: DiffFormula "H -1 Na 1" xsd:string
-property_value: DiffMono "21.981944" xsd:float
-property_value: Formula "C 4 H 4 N 1 Na 1 O 3" xsd:string
-property_value: MassAvg "137.07" xsd:float
-property_value: MassMono "137.008887" xsd:float
-property_value: Origin "D" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:30
-is_a: MOD:00423
-is_a: MOD:00904
-
-[Term]
-id: MOD:01296
-name: monosodium L-glutamate
-def: "A protein modification that effectively converts an L-glutamic acid residue to monosodium L-glutamate." [PubMed:12216740, Unimod:30#E]
-subset: PSI-MOD-slim
-synonym: "Cation:Na" RELATED PSI-MS-label []
-synonym: "MSG" EXACT PSI-MOD-alternate []
-synonym: "Na1Glu" EXACT PSI-MOD-label []
-synonym: "Sodium adduct" RELATED Unimod-description []
-property_value: DiffAvg "21.98" xsd:float
-property_value: DiffFormula "H -1 Na 1" xsd:string
-property_value: DiffMono "21.981944" xsd:float
-property_value: Formula "C 5 H 6 N 1 Na 1 O 3" xsd:string
-property_value: MassAvg "151.10" xsd:float
-property_value: MassMono "151.024537" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:30
-is_a: MOD:00423
-is_a: MOD:00906
-
-[Term]
-id: MOD:01297
-name: 5x(13)C labeled L-proline
-def: "A protein modification that effectively converts an L-proline residue to 5x(13)C labeled L-proline." [PubMed:12716131, Unimod:772#P]
-comment: In PubMed:12716131, fully (13)C labeled proline apparently resulted from the catabolic conversion of (13)C labeled L-arginine during SILAC.
-synonym: "13C(5) Silac label" RELATED Unimod-description []
-synonym: "Label:13C(5)" RELATED PSI-MS-label []
-property_value: DiffAvg "5.02" xsd:float
-property_value: DiffFormula "(12)C -5 (13)C 5" xsd:string
-property_value: DiffMono "5.016774" xsd:float
-property_value: Formula "(13)C 5 H 7 N 1 O 1" xsd:string
-property_value: MassAvg "102.07" xsd:float
-property_value: MassMono "102.069538" xsd:float
-property_value: Origin "P" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:772
-is_a: MOD:00915
-is_a: MOD:01832
-
-[Term]
-id: MOD:01298
-name: reduced cysteine 4-hydroxynonenal adduct
-def: "A protein modification produced by formation of an adduct of an L-cysteine residue with 4-hydroxynonenal artificially reduced by a reagent such as NaBH4." [PubMed:11910026, PubMed:15133838, Unimod:335#C]
-comment: 4-hydroxynonenal, a toxic lipid aldehyde, is a product of the hydroperoxide beta-cleavage degradation of omega-6 polyunsaturated fatty acids, such as arachidonic and linoleic acids [JSG].
-synonym: "HNE+Delta:H(2)" RELATED PSI-MS-label []
-synonym: "reduced 4-Hydroxynonenal" RELATED Unimod-description []
-property_value: DiffAvg "158.24" xsd:float
-property_value: DiffFormula "C 9 H 18 O 2" xsd:string
-property_value: DiffMono "158.130680" xsd:float
-property_value: Formula "C 12 H 23 N 1 O 3 S 1" xsd:string
-property_value: MassAvg "261.38" xsd:float
-property_value: MassMono "261.139865" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:335
-is_a: MOD:00642
-is_a: MOD:00905
-relationship: derives_from MOD:01237
-
-[Term]
-id: MOD:01299
-name: reduced lysine 4-hydroxynonenal adduct
-def: "A protein modification produced by formation of an adduct of an L-histidine residue with 4-hydroxynonenal artificially reduced by a reagent such as NaBH4." [PubMed:11910026, PubMed:12148805, PubMed:15133838, Unimod:335#K]
-comment: 4-hydroxynonenal, a toxic lipid aldehyde, is a product of the hydroperoxide beta-cleavage degradation of omega-6 polyunsaturated fatty acids, such as arachidonic and linoleic acids [JSG].
-synonym: "HNE+Delta:H(2)" RELATED PSI-MS-label []
-synonym: "reduced 4-Hydroxynonenal" RELATED Unimod-description []
-property_value: DiffAvg "158.24" xsd:float
-property_value: DiffFormula "C 9 H 18 O 2" xsd:string
-property_value: DiffMono "158.130680" xsd:float
-property_value: Formula "C 15 H 30 N 2 O 3" xsd:string
-property_value: MassAvg "286.42" xsd:float
-property_value: MassMono "286.225643" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:335
-is_a: MOD:00642
-is_a: MOD:00912
-relationship: derives_from MOD:01238
-
-[Term]
-id: MOD:01300
-name: reduced histidine 4-hydroxynonenal adduct
-def: "A protein modification produced by formation of an adduct of an L-histidine residue with 4-hydroxynonenal artificially reduced by a reagent such as NaBH4." [PubMed:11910026, PubMed:12148805, PubMed:15133838, Unimod:335#H]
-comment: 4-hydroxynonenal, a toxic lipid aldehyde, is a product of the hydroperoxide beta-cleavage degradation of omega-6 polyunsaturated fatty acids, such as arachidonic and linoleic acids [JSG].
-synonym: "HNE+Delta:H(2)" RELATED PSI-MS-label []
-synonym: "reduced 4-Hydroxynonenal" RELATED Unimod-description []
-property_value: DiffAvg "158.24" xsd:float
-property_value: DiffFormula "C 9 H 18 O 2" xsd:string
-property_value: DiffMono "158.130680" xsd:float
-property_value: Formula "C 15 H 25 N 3 O 3" xsd:string
-property_value: MassAvg "295.38" xsd:float
-property_value: MassMono "295.189592" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:335
-is_a: MOD:00642
-is_a: MOD:00909
-relationship: derives_from MOD:01239
-
-[Term]
-id: MOD:01301
-name: methylamine Michael addition derivatized threonine
-def: "A protein modification that effectively converts an L-threonine residue to 2-amino-3-(methylamino)butanoic acid." [PubMed:11743741, Unimod:337#T]
-comment: In PubMed:11743741 phosphothreonine is converted to dehydrobutyrine in base, then by Michael addition of methylamine to 2-amino-3-(methylamino)butanoic acid.
-synonym: "Methylamine" RELATED PSI-MS-label []
-synonym: "Michael addition with methylamine" RELATED Unimod-description []
-property_value: DiffAvg "13.04" xsd:float
-property_value: DiffFormula "C 1 H 3 N 1 O -1" xsd:string
-property_value: DiffMono "13.031634" xsd:float
-property_value: Formula "C 5 H 10 N 2 O 1" xsd:string
-property_value: MassAvg "114.15" xsd:float
-property_value: MassMono "114.079313" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:337
-is_a: MOD:00643
-is_a: MOD:00917
-
-[Term]
-id: MOD:01302
-name: methylamine Michael addition derivatized serine
-def: "A protein modification that effectively converts an L-serine residue to 2-amino-3-(methylamino)propanoic acid." [PubMed:11743741, Unimod:337#S]
-comment: In PubMed:11743741 phosphoserine is converted to dehydroalanine in base, then by Michael addition of methylamine to 2-amino-3-(methylamino)propanoic acid.
-synonym: "Methylamine" RELATED PSI-MS-label []
-synonym: "Michael addition with methylamine" RELATED Unimod-description []
-property_value: DiffAvg "13.04" xsd:float
-property_value: DiffFormula "C 1 H 3 N 1 O -1" xsd:string
-property_value: DiffMono "13.031634" xsd:float
-property_value: Formula "C 4 H 8 N 2 O 1" xsd:string
-property_value: MassAvg "100.12" xsd:float
-property_value: MassMono "100.063663" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:337
-is_a: MOD:00643
-is_a: MOD:00916
-
-[Term]
-id: MOD:01303
-name: N4-hexosaminylated asparagine
-def: "A protein modification that effectively converts an L-asparagine residue to an N4-hexosaminyl-L-asparagine." [PubMed:11467524, Unimod:454#N]
-comment: The natural modifications are N4-(N-acetylamino)galactosyl-L-asparagine (MOD:00832) or N4-(N-acetylamino)glucosyl-L-asparagine (MOD:00831) [JSG].
-synonym: "HexN" RELATED PSI-MS-label []
-synonym: "Hexosamine" RELATED Unimod-description []
-property_value: DiffAvg "161.16" xsd:float
-property_value: DiffFormula "C 6 H 11 N 1 O 4" xsd:string
-property_value: DiffMono "161.068808" xsd:float
-property_value: Formula "C 10 H 17 N 3 O 6" xsd:string
-property_value: MassAvg "275.26" xsd:float
-property_value: MassMono "275.111735" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:454
-is_a: MOD:00160
-is_a: MOD:00876
-
-[Term]
-id: MOD:01304
-name: N6-hexosaminylated lysine
-def: "A protein modification that effectively converts an L-lysine residue to an N4-hexosaminyl-L-lysine, as a synthetic peptide protectting group." [Unimod:454#K]
-synonym: "HexN" RELATED PSI-MS-label []
-synonym: "Hexosamine" RELATED Unimod-description []
-property_value: DiffAvg "161.16" xsd:float
-property_value: DiffFormula "C 6 H 11 N 1 O 4" xsd:string
-property_value: DiffMono "161.068808" xsd:float
-property_value: Formula "C 12 H 23 N 3 O 5" xsd:string
-property_value: MassAvg "289.33" xsd:float
-property_value: MassMono "289.163771" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:454
-is_a: MOD:00876
-is_a: MOD:00912
-
-[Term]
-id: MOD:01305
-name: N1'-hexosaminylated tryptophan
-def: "A protein modification that effectively converts an L-tryptophan residue to N1'-hexosaminyl-L-tryptophan." [Unimod:454#W]
-comment: The natural modification is N1'-mannosyl-L-tryptophan (MOD:00165) [JSG].
-synonym: "HexN" RELATED PSI-MS-label []
-synonym: "Hexosamine" RELATED Unimod-description []
-property_value: DiffAvg "161.16" xsd:float
-property_value: DiffFormula "C 6 H 11 N 1 O 4" xsd:string
-property_value: DiffMono "161.068808" xsd:float
-property_value: Formula "C 17 H 21 N 3 O 5" xsd:string
-property_value: MassAvg "347.37" xsd:float
-property_value: MassMono "347.148121" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:454
-is_a: MOD:00876
-is_a: MOD:00918
-
-[Term]
-id: MOD:01306
-name: O-hexosaminylated threonine
-def: "A protein modification that effectively converts an L-threonine residue to O-hexosaminyl-L-threonine." [Unimod:454#T]
-comment: The natural modifications are O-(N-acetylaminogalactosyl)-L-threonine (MOD:00164) or O-(N-acetylaminoglucosyl)-L-threonine (MOD:00806) [JSG].
-synonym: "HexN" RELATED PSI-MS-label []
-synonym: "Hexosamine" RELATED Unimod-description []
-property_value: DiffAvg "161.16" xsd:float
-property_value: DiffFormula "C 6 H 11 N 1 O 4" xsd:string
-property_value: DiffMono "161.068808" xsd:float
-property_value: Formula "C 10 H 18 N 2 O 6" xsd:string
-property_value: MassAvg "262.26" xsd:float
-property_value: MassMono "262.116486" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:454
-is_a: MOD:00005
-is_a: MOD:00876
-
-[Term]
-id: MOD:01307
-name: thiophosphate labeled with biotin-HPDP -site S
-def: "modification from Unimod Chemical derivative -" [Unimod:332#S]
-synonym: "Thiophos-S-S-biotin" RELATED PSI-MS-label []
-synonym: "thiophosphate labeled with biotin-HPDP" RELATED Unimod-description []
-property_value: DiffAvg "525.66" xsd:float
-property_value: DiffFormula "C 19 H 34 N 4 O 5 P 1 S 3" xsd:string
-property_value: DiffMono "525.142895" xsd:float
-property_value: Formula "C 22 H 39 N 5 O 7 P 1 S 3" xsd:string
-property_value: MassAvg "612.74" xsd:float
-property_value: MassMono "612.174923" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:332
-is_a: MOD:00639
-is_a: MOD:00916
-
-[Term]
-id: MOD:01308
-name: thiophosphate labeled with biotin-HPDP -site T
-def: "modification from Unimod Chemical derivative -" [Unimod:332#T]
-synonym: "Thiophos-S-S-biotin" RELATED PSI-MS-label []
-synonym: "thiophosphate labeled with biotin-HPDP" RELATED Unimod-description []
-property_value: DiffAvg "525.66" xsd:float
-property_value: DiffFormula "C 19 H 34 N 4 O 5 P 1 S 3" xsd:string
-property_value: DiffMono "525.142895" xsd:float
-property_value: Formula "C 23 H 41 N 5 O 7 P 1 S 3" xsd:string
-property_value: MassAvg "626.76" xsd:float
-property_value: MassMono "626.190573" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:332
-is_a: MOD:00639
-is_a: MOD:00917
-
-[Term]
-id: MOD:01309
-name: thiophosphate labeled with biotin-HPDP - site Y
-def: "modification from Unimod Chemical derivative - " [Unimod:332#Y]
-synonym: "Thiophos-S-S-biotin" RELATED PSI-MS-label []
-synonym: "thiophosphate labeled with biotin-HPDP" RELATED Unimod-description []
-property_value: DiffAvg "525.66" xsd:float
-property_value: DiffFormula "C 19 H 34 N 4 O 5 P 1 S 3" xsd:string
-property_value: DiffMono "525.142895" xsd:float
-property_value: Formula "C 28 H 43 N 5 O 7 P 1 S 3" xsd:string
-property_value: MassAvg "688.83" xsd:float
-property_value: MassMono "688.206223" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:332
-is_a: MOD:00639
-is_a: MOD:00919
-
-[Term]
-id: MOD:01310
-name: quaternary amine labeling reagent light form N6-L-lysine
-def: "A protein modification that effectively replaces a lysine N6-hydrogen with a quaternary amine reagent light form group." [PubMed:11857757, Unimod:60#K]
-synonym: "GIST-Quat" RELATED PSI-MS-label []
-synonym: "Quaternary amine labeling reagent light form (N-term & K)" RELATED Unimod-description []
-property_value: DiffAvg "59.07" xsd:float
-property_value: DiffFormula "C 3 (1)H 9 N 1" xsd:string
-property_value: DiffMono "59.073499" xsd:float
-property_value: Formula "C 9 (1)H 21 N 3 O 1" xsd:string
-property_value: MassAvg "187.17" xsd:float
-property_value: MassMono "187.168462" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:60
-is_a: MOD:00912
-is_a: MOD:01426
-
-[Term]
-id: MOD:01311
-name: quaternary amine labeling reagent heavy form (+3amu) N6-L-lysine
-def: "A protein modification that effectively replaces a lysine N6-hydrogen with a quaternary amine reagent heavy (+3amu) form group." [PubMed:11698400, PubMed:11857757, PubMed:11914093, Unimod:61#K]
-synonym: "GIST-Quat:2H(3)" RELATED PSI-MS-label []
-synonym: "Quaternary amine labeling reagent heavy (+3amu) form, N-term & K" RELATED Unimod-description []
-property_value: DiffAvg "62.09" xsd:float
-property_value: DiffFormula "C 3 (1)H 6 (2)H 3 N 1" xsd:string
-property_value: DiffMono "62.092330" xsd:float
-property_value: Formula "C 9 (1)H 18 (2)H 3 N 3 O 1" xsd:string
-property_value: MassAvg "190.19" xsd:float
-property_value: MassMono "190.187293" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:61
-is_a: MOD:00912
-is_a: MOD:01426
-
-[Term]
-id: MOD:01312
-name: quaternary amine labeling reagent heavy form (+6amu) N6-L-lysine
-def: "A protein modification that effectively replaces a lysine N6-hydrogen with a quaternary amine reagent heavy (+6amu) form group." [PubMed:11857757, Unimod:62#K]
-comment: Apparently incorrect parent [JSG].
-synonym: "GIST-Quat:2H(6)" RELATED PSI-MS-label []
-synonym: "Quaternary amine labeling reagent heavy form (+6amu), N-term & K" RELATED Unimod-description []
-property_value: DiffAvg "65.11" xsd:float
-property_value: DiffFormula "C 3 (1)H 3 (2)H 6 N 1" xsd:string
-property_value: DiffMono "65.111160" xsd:float
-property_value: Formula "C 9 (1)H 15 (2)H 6 N 3 O 1" xsd:string
-property_value: MassAvg "193.21" xsd:float
-property_value: MassMono "193.206123" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:62
-is_a: MOD:00912
-is_a: MOD:01426
-
-[Term]
-id: MOD:01313
-name: quaternary amine labeling reagent heavy form (+9amu) N6-L-lysine
-def: "A protein modification that effectively replaces a lysine N6-hydrogen with a quaternary amine reagent heavy (+9amu) form group." [PubMed:11857757, Unimod:63#K]
-synonym: "GIST-Quat:2H(9)" RELATED PSI-MS-label []
-synonym: "Quaternary amine labeling reagent heavy form (+9amu), N-term & K" RELATED Unimod-description []
-property_value: DiffAvg "68.13" xsd:float
-property_value: DiffFormula "C 3 (2)H 9 N 1" xsd:string
-property_value: DiffMono "68.129990" xsd:float
-property_value: Formula "C 9 (1)H 12 (2)H 9 N 3 O 1" xsd:string
-property_value: MassAvg "196.22" xsd:float
-property_value: MassMono "196.224953" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:63
-is_a: MOD:00912
-is_a: MOD:01426
-
-[Term]
-id: MOD:01314
-name: 4x(1)H,4x(12)C-labeled N6-succinyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to 4x(1)H,4x(12)C-labeled N6-succinyl-L-lysine." [PubMed:11857757, PubMed:12175151, PubMed:12716131, Unimod:64#K]
-synonym: "Succinic anhydride labeling reagent light form (K)" RELATED Unimod-description []
-synonym: "Succinyl" RELATED PSI-MS-label []
-property_value: DiffAvg "100.02" xsd:float
-property_value: DiffFormula "(12)C 4 (1)H 4 O 3" xsd:string
-property_value: DiffMono "100.016044" xsd:float
-property_value: Formula "(12)C 10 H 16 N 2 O 4" xsd:string
-property_value: MassAvg "228.11" xsd:float
-property_value: MassMono "228.111007" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:64
-relationship: derives_from MOD:01819
-is_a: MOD:00670
-is_a: MOD:01426
-
-[Term]
-id: MOD:01315
-name: 4x(2)H labeled N6-succinyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to 4x(2)H-labeled N6-succinyl-L-lysine." [PubMed:11344537, PubMed:11857757, PubMed:12175151, PubMed:15189151, Unimod:65#K]
-synonym: "Succinic anhydride labeling reagent, heavy form (+4amu, 4H2), N-term & K" RELATED Unimod-description []
-synonym: "Succinyl:2H(4)" RELATED PSI-MS-label []
-property_value: DiffAvg "104.04" xsd:float
-property_value: DiffFormula "C 4 (2)H 4 O 3" xsd:string
-property_value: DiffMono "104.041151" xsd:float
-property_value: Formula "C 10 (1)H 12 (2)H 4 N 2 O 4" xsd:string
-property_value: MassAvg "232.14" xsd:float
-property_value: MassMono "232.136114" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:65
-relationship: derives_from MOD:01819
-is_a: MOD:00670
-is_a: MOD:01426
-
-[Term]
-id: MOD:01316
-name: 4x(13)C labeled N6-succinyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to 4x(13)C labeled N6-succinyl-L-lysine." [PubMed:11344537, PubMed:11857757, PubMed:12175151, PubMed:15189151, Unimod:66#K]
-synonym: "Succinic anhydride labeling reagent, heavy form (+4amu, 4C13),  K" RELATED Unimod-description []
-synonym: "Succinyl:13C(4)" RELATED PSI-MS-label []
-property_value: DiffAvg "104.03" xsd:float
-property_value: DiffFormula "(13)C 4 H 4 O 3" xsd:string
-property_value: DiffMono "104.029463" xsd:float
-property_value: Formula "(12)C 6 (13)C 4 H 16 N 2 O 4" xsd:string
-property_value: MassAvg "232.12" xsd:float
-property_value: MassMono "232.124426" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:66
-relationship: derives_from MOD:01819
-is_a: MOD:00670
-is_a: MOD:01428
-
-[Term]
-id: MOD:01317
-name: phosphorylation to amine thiol - site T
-def: "modification from Unimod Chemical derivative -" [PubMed:12216740, Unimod:178#T]
-synonym: "DAET" RELATED PSI-MS-label []
-synonym: "phosphorylation to amine thiol" RELATED Unimod-description []
-property_value: DiffAvg "87.18" xsd:float
-property_value: DiffFormula "C 4 H 9 N 1 O -1 S 1" xsd:string
-property_value: DiffMono "87.050656" xsd:float
-property_value: Formula "C 8 H 16 N 2 O 1 S 1" xsd:string
-property_value: MassAvg "188.29" xsd:float
-property_value: MassMono "188.098334" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:178
-is_a: MOD:00535
-is_a: MOD:00917
-
-[Term]
-id: MOD:01318
-name: phosphorylation to amine thiol - site S
-def: "modification from Unimod Chemical derivative -" [PubMed:11510821, PubMed:12216740, PubMed:12422359, Unimod:178#S]
-synonym: "DAET" RELATED PSI-MS-label []
-synonym: "phosphorylation to amine thiol" RELATED Unimod-description []
-property_value: DiffAvg "87.18" xsd:float
-property_value: DiffFormula "C 4 H 9 N 1 O -1 S 1" xsd:string
-property_value: DiffMono "87.050656" xsd:float
-property_value: Formula "C 7 H 14 N 2 O 1 S 1" xsd:string
-property_value: MassAvg "174.26" xsd:float
-property_value: MassMono "174.082684" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:178
-is_a: MOD:00535
-is_a: MOD:00916
-
-[Term]
-id: MOD:01319
-name: Michael addition of BHT quinone methide to histidine
-def: "modification from Unimod Other" [PubMed:11510821, PubMed:12422359, PubMed:9448752, Unimod:176#H]
-comment: Secondary adduct, much less common than cysteine. [Unimod]
-synonym: "BHT" RELATED PSI-MS-label []
-synonym: "Michael addition of BHT quinone methide to Cysteine and Lysine" RELATED Unimod-description []
-property_value: DiffAvg "218.34" xsd:float
-property_value: DiffFormula "C 15 H 22 O 1" xsd:string
-property_value: DiffMono "218.167065" xsd:float
-property_value: Formula "C 21 H 29 N 3 O 2" xsd:string
-property_value: MassAvg "355.48" xsd:float
-property_value: MassMono "355.225977" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:176
-is_a: MOD:00534
-is_a: MOD:00909
-
-[Term]
-id: MOD:01320
-name: Michael addition of BHT quinone methide to lysine
-def: "modification from Unimod Other" [PubMed:16078144, PubMed:9448752, Unimod:176#K]
-comment: Secondary adduct, much less common than cysteine. [Unimod]
-synonym: "BHT" RELATED PSI-MS-label []
-synonym: "Michael addition of BHT quinone methide to Cysteine and Lysine" RELATED Unimod-description []
-property_value: DiffAvg "218.34" xsd:float
-property_value: DiffFormula "C 15 H 22 O 1" xsd:string
-property_value: DiffMono "218.167065" xsd:float
-property_value: Formula "C 21 H 34 N 2 O 2" xsd:string
-property_value: MassAvg "346.51" xsd:float
-property_value: MassMono "346.262028" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:176
-is_a: MOD:00534
-is_a: MOD:00912
-
-[Term]
-id: MOD:01321
-name: Michael addition of BHT quinone methide to cysteine
-def: "modification from Unimod Other" [PubMed:11510821, PubMed:12422359, PubMed:9448752, Unimod:176#C]
-comment: Primary adduct formed. [Unimod]
-synonym: "BHT" RELATED PSI-MS-label []
-synonym: "Michael addition of BHT quinone methide to Cysteine and Lysine" RELATED Unimod-description []
-property_value: DiffAvg "218.34" xsd:float
-property_value: DiffFormula "C 15 H 22 O 1" xsd:string
-property_value: DiffMono "218.167065" xsd:float
-property_value: Formula "C 18 H 27 N 1 O 2 S 1" xsd:string
-property_value: MassAvg "321.48" xsd:float
-property_value: MassMono "321.176250" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:176
-is_a: MOD:00534
-is_a: MOD:00905
-
-[Term]
-id: MOD:01322
-name: propionaldehyde +40 - site K
-def: "OBSOLETE because not supported by the linked literature [PMT]. modification from Unimod Other -" [PubMed:15549660, Unimod:256#K]
-synonym: "Delta:H(4)C(3)" RELATED PSI-MS-label []
-synonym: "Propionaldehyde +40" RELATED Unimod-description []
-property_value: DiffAvg "40.06" xsd:float
-property_value: DiffFormula "C 3 H 4" xsd:string
-property_value: DiffMono "40.031300" xsd:float
-property_value: Formula "C 9 H 16 N 2 O 1" xsd:string
-property_value: MassAvg "168.24" xsd:float
-property_value: MassMono "168.126263" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:256
-is_obsolete: true
-
-[Term]
-id: MOD:01323
-name: propionaldehyde +40 - site H
-def: "OBSOLETE because not supported by the linked literature [PMT]. modification from Unimod Other -" [Unimod:256#H]
-synonym: "Delta:H(4)C(3)" RELATED PSI-MS-label []
-synonym: "Propionaldehyde +40" RELATED Unimod-description []
-property_value: DiffAvg "40.06" xsd:float
-property_value: DiffFormula "C 3 H 4" xsd:string
-property_value: DiffMono "40.031300" xsd:float
-property_value: Formula "C 9 H 11 N 3 O 1" xsd:string
-property_value: MassAvg "177.21" xsd:float
-property_value: MassMono "177.090212" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:256
-is_obsolete: true
-
-[Term]
-id: MOD:01324
-name: acetaldehyde +26 - site H
-def: "OBSOLETE because this is not supported by the linked literature [PMT]" [PubMed:7744761, Unimod:254#H]
-synonym: "Acetaldehyde +26" RELATED Unimod-description []
-synonym: "Delta:H(2)C(2)" RELATED PSI-MS-label []
-property_value: DiffAvg "26.04" xsd:float
-property_value: DiffFormula "C 2 H 2" xsd:string
-property_value: DiffMono "26.015650" xsd:float
-property_value: Formula "C 8 H 9 N 3 O 1" xsd:string
-property_value: MassAvg "163.18" xsd:float
-property_value: MassMono "163.074562" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:254
-is_obsolete: true
-
-[Term]
-id: MOD:01325
-name: acetaldehyde +26 - site K
-def: "OBSOLETE because this is not supported by the linked literature [PMT]" [PubMed:7744761, Unimod:254#K]
-synonym: "Acetaldehyde +26" RELATED Unimod-description []
-synonym: "Delta:H(2)C(2)" RELATED PSI-MS-label []
-property_value: DiffAvg "26.04" xsd:float
-property_value: DiffFormula "C 2 H 2" xsd:string
-property_value: DiffMono "26.015650" xsd:float
-property_value: Formula "C 8 H 14 N 2 O 1" xsd:string
-property_value: MassAvg "154.21" xsd:float
-property_value: MassMono "154.110613" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:254
-is_obsolete: true
-
-[Term]
-id: MOD:01326
-name: 9x(13)C labeled L-tyrosine
-def: "A protein modification that effectively converts an L-tyrosine residue to 9x(13)C labeled L-tyrosine." [PubMed:11510821, PubMed:12422359, PubMed:12716131, Unimod:184#Y]
-synonym: "13C(9) Silac label" RELATED Unimod-description []
-synonym: "Label:13C(9)" RELATED PSI-MS-label []
-property_value: DiffAvg "9.03" xsd:float
-property_value: DiffFormula "(12)C -9 (13)C 9" xsd:string
-property_value: DiffMono "9.030194" xsd:float
-property_value: Formula "(13)C 9 H 9 N 1 O 2" xsd:string
-property_value: MassAvg "172.09" xsd:float
-property_value: MassMono "172.093522" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:184
-is_a: MOD:00540
-is_a: MOD:00919
-
-[Term]
-id: MOD:01327
-name: 9x(13)C labeled L-phenylalanine
-def: "A protein modification that effectively converts an L-phenylalanine residue to 9x(13)C labeled L-phenylalanine." [PubMed:12716131, Unimod:184#F]
-synonym: "13C(9) Silac label" RELATED Unimod-description []
-synonym: "Label:13C(9)" RELATED PSI-MS-label []
-property_value: DiffAvg "9.03" xsd:float
-property_value: DiffFormula "(12)C -9 (13)C 9" xsd:string
-property_value: DiffMono "9.030194" xsd:float
-property_value: Formula "(13)C 9 H 9 N 1 O 1" xsd:string
-property_value: MassAvg "156.10" xsd:float
-property_value: MassMono "156.098607" xsd:float
-property_value: Origin "F" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:184
-is_a: MOD:00540
-is_a: MOD:00914
-
-[Term]
-id: MOD:01328
-name: iodoacetic acid - site W
-def: "modification from Unimod Chemical derivative - hydroxylethanone" [PubMed:17525468, Unimod:6#W]
-comment: There is no citation for this Unimod entry. Iodoacetic acid derivatization of tryptophan is not mentioned in the citation [JSG].
-synonym: "Carboxymethyl" RELATED PSI-MS-label []
-synonym: "Iodoacetic acid derivative" RELATED Unimod-description []
-property_value: DiffAvg "58.04" xsd:float
-property_value: DiffFormula "C 2 H 2 O 2" xsd:string
-property_value: DiffMono "58.005479" xsd:float
-property_value: Formula "C 13 H 12 N 2 O 3" xsd:string
-property_value: MassAvg "244.25" xsd:float
-property_value: MassMono "244.084792" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:6
-is_a: MOD:00399
-is_a: MOD:00918
-
-[Term]
-id: MOD:01329
-name: iodoacetic acid - site C
-def: "OBSOLETE because duplicate and redundant with MOD:01061. Remap to MOD:01061" [DeltaMass:197]
-comment: Modification from Unimod Chemical derivative, Unimod:6 site C
-synonym: "Carboxymethyl" RELATED PSI-MS-label []
-synonym: "Iodoacetic acid derivative" RELATED Unimod-description []
-property_value: DiffAvg "58.04" xsd:float
-property_value: DiffFormula "C 2 H 2 O 2" xsd:string
-property_value: DiffMono "58.005479" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-replaced_by: MOD:01061
-xref: Unimod:6
-is_obsolete: true
-
-[Term]
-id: MOD:01330
-name: iodoacetic acid -site K
-def: "OBSOLETE because identical with MOD:01094. Remap to MOD:01094" [PubMed:18688235]
-comment: a modification from Unimod:6
-synonym: "Carboxymethyl" RELATED PSI-MS-label []
-synonym: "Iodoacetic acid derivative" RELATED Unimod-description []
-property_value: DiffAvg "58.04" xsd:float
-property_value: DiffFormula "C 2 H 2 O 2" xsd:string
-property_value: DiffMono "58.005479" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-replaced_by: MOD:01094
-xref: Unimod:6
-is_obsolete: true
-
-[Term]
-id: MOD:01331
-name: 6x(13)C labeled L-arginine
-def: "A protein modification that effectively converts an L-arginine residue to 6x(13)C labeled L-arginine." [OMSSA:136, PubMed:12716131, Unimod:188#R]
-subset: PSI-MOD-slim
-synonym: "13C(6) Silac label" RELATED Unimod-description []
-synonym: "arg-13c6" EXACT OMSSA-label []
-synonym: "Label:13C(6)" RELATED PSI-MS-label []
-property_value: DiffAvg "6.02" xsd:float
-property_value: DiffFormula "(12)C -6 (13)C 6" xsd:string
-property_value: DiffMono "6.020129" xsd:float
-property_value: Formula "(13)C 6 H 12 N 4 O 1" xsd:string
-property_value: MassAvg "162.12" xsd:float
-property_value: MassMono "162.121240" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:188
-is_a: MOD:00544
-
-[Term]
-id: MOD:01332
-name: 6x(13)C labeled L-leucine
-def: "A protein modification that effectively converts an L-leucine residue to 6x(13)C labeled L-leucine." [PubMed:12716131, Unimod:188#L]
-subset: PSI-MOD-slim
-synonym: "13C(6) Silac label" RELATED Unimod-description []
-synonym: "Label:13C(6)" RELATED PSI-MS-label []
-property_value: DiffAvg "6.02" xsd:float
-property_value: DiffFormula "(12)C -6 (13)C 6" xsd:string
-property_value: DiffMono "6.020129" xsd:float
-property_value: Formula "(13)C 6 H 11 N 1 O 1" xsd:string
-property_value: MassAvg "119.10" xsd:float
-property_value: MassMono "119.104193" xsd:float
-property_value: Origin "L" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:188
-is_a: MOD:00544
-
-[Term]
-id: MOD:01333
-name: 6x(13)C labeled L-isoleucine
-def: "A protein modification that effectively converts an L-isoleucine residue to 6x(13)C labeled L-isoleucine." [PubMed:12716131, PubMed:12766232, Unimod:188#I]
-subset: PSI-MOD-slim
-synonym: "13C(6) Silac label" RELATED Unimod-description []
-synonym: "Label:13C(6)" RELATED PSI-MS-label []
-property_value: DiffAvg "6.02" xsd:float
-property_value: DiffFormula "(12)C -6 (13)C 6" xsd:string
-property_value: DiffMono "6.020129" xsd:float
-property_value: Formula "(13)C 6 H 11 N 1 O 1" xsd:string
-property_value: MassAvg "119.10" xsd:float
-property_value: MassMono "119.104193" xsd:float
-property_value: Origin "I" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:188
-is_a: MOD:00544
-
-[Term]
-id: MOD:01334
-name: 6x(13)C labeled L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to 6x(13)C labeled L-lysine." [OMSSA:138, PubMed:11857757, PubMed:11999733, PubMed:12175151, PubMed:12716131, Unimod:188#K]
-subset: PSI-MOD-slim
-synonym: "13C(6) Silac label" RELATED Unimod-description []
-synonym: "Label:13C(6)" RELATED PSI-MS-label []
-synonym: "lys-13c6" EXACT OMSSA-label []
-property_value: DiffAvg "6.02" xsd:float
-property_value: DiffFormula "(12)C -6 (13)C 6" xsd:string
-property_value: DiffMono "6.020129" xsd:float
-property_value: Formula "(13)C 6 H 12 N 2 O 1" xsd:string
-property_value: MassAvg "134.12" xsd:float
-property_value: MassMono "134.115092" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:188
-is_a: MOD:00544
-
-[Term]
-id: MOD:01335
-name: 6x(13)C labeled 4-sulfophenyl isothiocyanate derivatized lysine
-def: "modification from Unimod Chemical derivative -" [PubMed:11467524, PubMed:16526082, Unimod:464#K]
-synonym: "4-sulfophenyl isothiocyanate (Heavy C13)" RELATED Unimod-description []
-synonym: "SPITC:13C(6)" RELATED PSI-MS-label []
-property_value: DiffAvg "220.99" xsd:float
-property_value: DiffFormula "(12)C 1 (13)C 6 H 5 N 1 O 3 S 2" xsd:string
-property_value: DiffMono "220.991214" xsd:float
-property_value: Formula "(12)C 7 (13)C 6 H 17 N 3 O 4 S 2" xsd:string
-property_value: MassAvg "349.09" xsd:float
-property_value: MassMono "349.086177" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:464
-is_a: MOD:00880
-is_a: MOD:00912
-
-[Term]
-id: MOD:01336
-name: deamidation followed by a methylation -site Q
-def: "OBSOLETE - identical and redundant with MOD:00657. Remap to MOD:00657." [PubMed:18688235]
-comment: Modification from Unimod Post-translational - Unimod:528.
-synonym: "Deamidation followed by a methylation" RELATED Unimod-description []
-synonym: "Methyl+Deamidated" RELATED PSI-MS-label []
-property_value: DiffAvg "15.01" xsd:float
-property_value: DiffFormula "C 1 H 1 N -1 O 1" xsd:string
-property_value: DiffMono "14.999666" xsd:float
-property_value: Origin "Q" xsd:string
-property_value: Source "natural" xsd:string
-replaced_by: MOD:00657
-xref: Unimod:528
-is_obsolete: true
-
-[Term]
-id: MOD:01337
-name: deamidated 4-methyl esterified asparagine
-def: "A protein modification that effectively converts an L-asparagine residue to L-aspartate 4-methyl ester." [Unimod:528#N]
-comment: The deamidation and methylation of L-asparagine has not been reported as a natural modification. It is extremely unlikely that eukaryotes produce this modification, because a natural process that would form L-aspartic acid 4-methyl ester from either L-aspartic acid or L-asparagine would interfere with the D-aspartyl peptide repair mechanism [JSG].
-synonym: "Deamidation followed by a methylation" RELATED Unimod-description []
-synonym: "Methyl+Deamidated" RELATED PSI-MS-label []
-property_value: DiffAvg "15.01" xsd:float
-property_value: DiffFormula "C 1 H 1 N -1 O 1" xsd:string
-property_value: DiffMono "14.999666" xsd:float
-property_value: Formula "C 5 H 7 N 1 O 3" xsd:string
-property_value: MassAvg "129.12" xsd:float
-property_value: MassMono "129.042593" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:528
-relationship: derives_from MOD:01181
-is_a: MOD:01369
-
-[Term]
-id: MOD:01338
-name: N6-ethyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-ethyl-L-lysine." [PubMed:9629898, Unimod:280#K]
-comment: The Unimod citation refers to the formation of glutamate ethyl ester and not to either lysine or N-terminal alkylation [JSG].
-synonym: "Ethyl" RELATED PSI-MS-label []
-synonym: "Ethylation" RELATED Unimod-description []
-property_value: DiffAvg "28.05" xsd:float
-property_value: DiffFormula "C 2 H 4" xsd:string
-property_value: DiffMono "28.031300" xsd:float
-property_value: Formula "C 8 H 16 N 2 O 1" xsd:string
-property_value: MassAvg "156.23" xsd:float
-property_value: MassMono "156.126263" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: Unimod:280
-is_a: MOD:00912
-is_a: MOD:01339
-
-[Term]
-id: MOD:01339
-name: ethylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with an ethyl group." [PubMed:9629898, Unimod:280]
-comment: From DeltaMass: Average Mass: 28 with no citation. The Unimod citation refers to the formation of glutamate ethyl ester and not to either lysine or N-terminal alkylation [JSG].
-synonym: "Ethyl" RELATED PSI-MS-label []
-synonym: "Ethylation" RELATED Unimod-description []
-synonym: "EtRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "28.05" xsd:float
-property_value: DiffFormula "C 2 H 4" xsd:string
-property_value: DiffMono "28.031300" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:280
-is_a: MOD:00001
-
-[Term]
-id: MOD:01340
-name: ESP-Tag heavy d10 - site K
-def: "modification from Unimod Isotopic label -" [PubMed:11078590, PubMed:11085420, PubMed:11821862, Unimod:91#K]
-synonym: "ESP-Tag heavy d10" RELATED Unimod-description []
-synonym: "ESP:2H(10)" RELATED PSI-MS-label []
-property_value: DiffAvg "348.24" xsd:float
-property_value: DiffFormula "C 16 (1)H 16 (2)H 10 N 4 O 2 S 1" xsd:string
-property_value: DiffMono "348.240415" xsd:float
-property_value: Formula "C 22 (1)H 28 (2)H 10 N 6 O 3 S 1" xsd:string
-property_value: MassAvg "476.34" xsd:float
-property_value: MassMono "476.335378" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:91
-is_a: MOD:00469
-is_a: MOD:00912
-
-[Term]
-id: MOD:01341
-name: ESP-Tag light d0 - site K
-def: "modification from Unimod Isotopic label -" [Unimod:90#K]
-synonym: "ESP" RELATED PSI-MS-label []
-synonym: "ESP-Tag light d0" RELATED Unimod-description []
-property_value: DiffAvg "338.47" xsd:float
-property_value: DiffFormula "C 16 H 26 N 4 O 2 S 1" xsd:string
-property_value: DiffMono "338.177647" xsd:float
-property_value: Formula "C 22 H 38 N 6 O 3 S 1" xsd:string
-property_value: MassAvg "466.64" xsd:float
-property_value: MassMono "466.272610" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:90
-is_a: MOD:00468
-is_a: MOD:00912
-
-[Term]
-id: MOD:01342
-name: selenium substitution for sulfur - site M
-def: "OBSOLETE because redundant and identical to MOD:00530. Remap to MOD:00530." [PubMed:12148805, Unimod:162]
-synonym: "Delta:S(-1)Se(1)" RELATED PSI-MS-label []
-synonym: "Selenium replaces sulphur" RELATED Unimod-description []
-property_value: DiffAvg "46.91" xsd:float
-property_value: DiffFormula "S -1 Se 1" xsd:string
-property_value: DiffMono "47.944450" xsd:float
-property_value: Formula "C 5 H 9 N 1 O 1 S 0 Se 1" xsd:string
-property_value: MassAvg "178.10" xsd:float
-property_value: MassMono "178.984935" xsd:float
-property_value: Origin "M" xsd:string
-property_value: Source "artifact" xsd:string
-replaced_by: MOD:00530
-xref: Unimod:162
-is_obsolete: true
-
-[Term]
-id: MOD:01343
-name: selenium substitution for sulfur - site C
-def: "OBSOLETE because redundant and identical to MOD:00686. Remap to MOD:00686." [PubMed:12148805, Unimod:162]
-synonym: "Delta:S(-1)Se(1)" RELATED PSI-MS-label []
-synonym: "Selenium replaces sulphur" RELATED Unimod-description []
-property_value: DiffAvg "46.91" xsd:float
-property_value: DiffFormula "S -1 Se 1" xsd:string
-property_value: DiffMono "47.944450" xsd:float
-property_value: Formula "C 3 H 5 N 1 O 1 S 0 Se 1" xsd:string
-property_value: MassAvg "150.05" xsd:float
-property_value: MassMono "150.953635" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-replaced_by: MOD:00686
-xref: Unimod:162
-is_obsolete: true
-
-[Term]
-id: MOD:01344
-name: dehydrogenated residue - site S
-def: "OBSOLETE because redundant and identical with MOD:00835. Remap to MOD:00835." [PubMed:9252331, PubMed:9276974, Unimod:401]
-synonym: "2-amino-3-oxo-butanoic_acid" RELATED Unimod-description []
-synonym: "Didehydro" RELATED PSI-MS-label []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "H -2" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-replaced_by: MOD:00835
-xref: Unimod:401
-is_obsolete: true
-
-[Term]
-id: MOD:01345
-name: 2-amino-3-oxobutanoic acid
-def: "A protein modification that effectively converts an L-threonine residue to 2-amino-3-oxobutanoic acid." [OMSSA:23, PubMed:12716131, PubMed:9252331, Unimod:401#T]
-comment: There is no citation for this modification in the Unimod entry. Although mentioned in PubMed:9252331, there is no citation for it there [JSG].
-synonym: "2-amino-3-ketobutyric acid" EXACT PSI-MOD-alternate []
-synonym: "2-amino-3-oxo-butanoic_acid" RELATED Unimod-description []
-synonym: "3-ketobutyrine" EXACT PSI-MOD-alternate []
-synonym: "Didehydro" RELATED PSI-MS-label []
-synonym: "twoamino3oxobutanoicacid" EXACT OMSSA-label []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "H -2" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 4 H 5 N 1 O 2" xsd:string
-property_value: MassAvg "99.09" xsd:float
-property_value: MassMono "99.032028" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:401
-is_a: MOD:00917
-is_a: MOD:01888
-
-[Term]
-id: MOD:01346
-name: N4-hexosylated asparagine
-def: "A protein modification that effectively converts an L-asparagine residue to an N4-hexosyl-L-asparagine." [PubMed:11112526, PubMed:11567090, PubMed:15279557, PubMed:6540775, Unimod:41#N]
-synonym: "Hex" RELATED PSI-MS-label []
-synonym: "Hexose" RELATED Unimod-description []
-property_value: DiffAvg "162.14" xsd:float
-property_value: DiffFormula "C 6 H 10 O 5" xsd:string
-property_value: DiffMono "162.052823" xsd:float
-property_value: Formula "C 10 H 16 N 2 O 7" xsd:string
-property_value: MassAvg "276.25" xsd:float
-property_value: MassMono "276.095751" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:41
-is_a: MOD:00160
-is_a: MOD:00434
-
-[Term]
-id: MOD:01347
-name: hexose glycated L-lysine
-def: "A modification produced in a non-enzymatic reaction between a carbohydrate carbonyl group (C1 of aldohexose or C2 of fructose) and an L-lysine residue to form a Schiff-base or an Amadori ketosamine lysine adduct." [DeltaMass:0, PubMed:15279557, Unimod:41#K]
-synonym: "Hex" RELATED PSI-MS-label []
-synonym: "Hexose" RELATED Unimod-description []
-property_value: DiffAvg "162.14" xsd:float
-property_value: DiffFormula "C 6 H 10 O 5" xsd:string
-property_value: DiffMono "162.052823" xsd:float
-property_value: Formula "C 12 H 22 N 2 O 6" xsd:string
-property_value: MassAvg "290.32" xsd:float
-property_value: MassMono "290.147786" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:41
-is_a: MOD:00767
-is_a: MOD:00912
-
-[Term]
-id: MOD:01348
-name: O-hexosylated threonine
-def: "A protein modification that effectively converts an L-threonine residue to an O-hexosyl-L-threonine." [PubMed:15279557, PubMed:8597590, Unimod:41#T]
-synonym: "Hex" RELATED PSI-MS-label []
-synonym: "Hexose" RELATED Unimod-description []
-property_value: DiffAvg "162.14" xsd:float
-property_value: DiffFormula "C 6 H 10 O 5" xsd:string
-property_value: DiffMono "162.052823" xsd:float
-property_value: Formula "C 10 H 17 N 1 O 7" xsd:string
-property_value: MassAvg "263.25" xsd:float
-property_value: MassMono "263.100502" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:41
-is_a: MOD:00005
-is_a: MOD:00434
-
-[Term]
-id: MOD:01349
-name: hydrolyzed N-ethylmaleimide cysteine adduct
-def: "modification from Unimod Chemical derivative -" [Unimod:320#C]
-comment: Hydolyzed N-ethylmaeimide adduct, a mixture of isobaric 2- and 3-(S-cysteinyl)-4-(ethylamino)-4-oxobutanoic acid [JSG].
-synonym: "Nethylmaleimide+water" RELATED PSI-MS-label []
-synonym: "Nethylmaleimidehydrolysis" RELATED Unimod-description []
-property_value: DiffAvg "143.14" xsd:float
-property_value: DiffFormula "C 6 H 9 N 1 O 3" xsd:string
-property_value: DiffMono "143.058243" xsd:float
-property_value: Formula "C 9 H 14 N 2 O 4 S 1" xsd:string
-property_value: MassAvg "246.28" xsd:float
-property_value: MassMono "246.067428" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:320
-is_a: MOD:00631
-is_a: MOD:00905
-
-[Term]
-id: MOD:01350
-name: hydrolyzed N-ethylmaleimide lysine adduct
-def: "modification from Unimod Chemical derivative -" [Unimod:320#K]
-comment: Hydolyzed N-ethylmaeimide adduct, a mixture of isobaric 2- and 3-(N6-lysyl)-4-(ethylamino)-4-oxobutanoic acid [JSG].
-synonym: "Nethylmaleimide+water" RELATED PSI-MS-label []
-synonym: "Nethylmaleimidehydrolysis" RELATED Unimod-description []
-property_value: DiffAvg "143.14" xsd:float
-property_value: DiffFormula "C 6 H 9 N 1 O 3" xsd:string
-property_value: DiffMono "143.058243" xsd:float
-property_value: Formula "C 12 H 21 N 3 O 4" xsd:string
-property_value: MassAvg "271.32" xsd:float
-property_value: MassMono "271.153206" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:320
-is_a: MOD:00631
-
-[Term]
-id: MOD:01351
-name: nitrated L-tryptophan
-def: "A protein modification that effectively converts an L-tryptophan residue to a nitrated L-tryptophan." [OMSSA:85, PubMed:8839040, PubMed:9252331, Unimod:354#W]
-comment: One or more isobaric isomers are produced by nitration with peroxynitrite reagent [JSG].
-synonym: "Nitro" RELATED PSI-MS-label []
-synonym: "nitrow" EXACT OMSSA-label []
-synonym: "Oxidation to nitro" RELATED Unimod-description []
-property_value: DiffAvg "45.00" xsd:float
-property_value: DiffFormula "H -1 N 1 O 2" xsd:string
-property_value: DiffMono "44.985078" xsd:float
-property_value: Formula "C 11 H 9 N 3 O 3" xsd:string
-property_value: MassAvg "231.21" xsd:float
-property_value: MassMono "231.064391" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:354
-is_a: MOD:00461
-is_a: MOD:00918
-
-[Term]
-id: MOD:01352
-name: nitrated L-tyrosine
-def: "A protein modification that effectively converts an L-tyrosine residue to a nitrated L-tyrosine." [OMSSA:86, PubMed:14678012, PubMed:8839040, PubMed:9252331, Unimod:354#Y]
-comment: One or more isobaric isomers are produced by nitration with peroxynitrite reagent [JSG].
-subset: PSI-MOD-slim
-synonym: "Nitro" RELATED PSI-MS-label []
-synonym: "nitroy" EXACT OMSSA-label []
-synonym: "Oxidation to nitro" RELATED Unimod-description []
-property_value: DiffAvg "45.00" xsd:float
-property_value: DiffFormula "H -1 N 1 O 2" xsd:string
-property_value: DiffMono "44.985078" xsd:float
-property_value: Formula "C 9 H 8 N 2 O 4" xsd:string
-property_value: MassAvg "208.17" xsd:float
-property_value: MassMono "208.048407" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:354
-xref: uniprot.ptm:PTM-0213
-is_a: MOD:00461
-is_a: MOD:00919
-
-[Term]
-id: MOD:01353
-name: amidination of lysines or N-terminal amines with methyl acetimidate - site K
-def: "modification from Unimod Chemical derivative -" [PubMed:12643539, PubMed:15602776, PubMed:6273432, Unimod:141#K]
-synonym: "amidination of lysines or N-terminal amines with methyl acetimidate" RELATED Unimod-description []
-synonym: "Amidine" RELATED PSI-MS-label []
-property_value: DiffAvg "41.05" xsd:float
-property_value: DiffFormula "C 2 H 3 N 1" xsd:string
-property_value: DiffMono "41.026549" xsd:float
-property_value: Formula "C 8 H 15 N 3 O 1" xsd:string
-property_value: MassAvg "169.23" xsd:float
-property_value: MassMono "169.121512" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:141
-is_a: MOD:00509
-is_a: MOD:00912
-
-[Term]
-id: MOD:01354
-name: Hex1HexNAc1NeuAc1 N4-glycosylated asparagine
-def: "A protein modification that effectively replaces an N4 hydrogen atom of an asparagine residue with a carbohydrate-like group composed of Hex1HexNAc1NeuAc1 linked through a glycosidic bond." [PubMed:11698400, Unimod:149#N]
-synonym: "Hex(1)HexNAc(1)NeuAc(1)" RELATED PSI-MS-label []
-synonym: "Hex1HexNAc1NeuAc1" RELATED Unimod-description []
-property_value: DiffAvg "657.60" xsd:float
-property_value: DiffFormula "C 25 H 41 N 2 O 18" xsd:string
-property_value: DiffMono "657.235437" xsd:float
-property_value: Formula "C 29 H 47 N 4 O 20" xsd:string
-property_value: MassAvg "771.70" xsd:float
-property_value: MassMono "771.278365" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:149
-is_a: MOD:00517
-is_a: MOD:00160
-
-[Term]
-id: MOD:01355
-name: Hex1HexNAc1NeuAc1 O-glycosylated threonine
-def: "A protein modification that effectively replaces an O3 hydrogen atom of a threonine residue with a carbohydrate-like group composed of Hex1HexNAc1NeuAc1 linked through a glycosidic bond." [Unimod:149#T]
-synonym: "Hex(1)HexNAc(1)NeuAc(1)" RELATED PSI-MS-label []
-synonym: "Hex1HexNAc1NeuAc1" RELATED Unimod-description []
-property_value: DiffAvg "657.60" xsd:float
-property_value: DiffFormula "C 25 H 41 N 2 O 18" xsd:string
-property_value: DiffMono "657.235437" xsd:float
-property_value: Formula "C 29 H 48 N 3 O 20" xsd:string
-property_value: MassAvg "758.70" xsd:float
-property_value: MassMono "758.283116" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:149
-is_a: MOD:00517
-is_a: MOD:00005
-
-[Term]
-id: MOD:01356
-name: Hex1HexNAc1NeuAc1 O-glycosylated serine
-def: "A protein modification that effectively replaces an O3 hydrogen atom of a serine residue with a carbohydrate-like group composed of Hex1HexNAc1NeuAc1 linked through a glycosidic bond." [PubMed:7856876, Unimod:149#S]
-synonym: "Hex(1)HexNAc(1)NeuAc(1)" RELATED PSI-MS-label []
-synonym: "Hex1HexNAc1NeuAc1" RELATED Unimod-description []
-property_value: DiffAvg "657.60" xsd:float
-property_value: DiffFormula "C 25 H 41 N 2 O 18" xsd:string
-property_value: DiffMono "657.235437" xsd:float
-property_value: Formula "C 28 H 46 N 3 O 20" xsd:string
-property_value: MassAvg "744.68" xsd:float
-property_value: MassMono "744.267466" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:149
-is_a: MOD:00517
-is_a: MOD:00916
-
-[Term]
-id: MOD:01357
-name: 2x(13)C,4x(2)H labeled dimethylated L-lysine
-def: "A protein modification that effectively replaces two hydrogen atoms of an L-lysine residue containing common isotopes with two (13)C,3x(2)H labeled methyl groups to form a 2x(13)C,6x(2)H labeled dimethylated L-lysine." [PubMed:12686488, PubMed:16335955, Unimod:510#K]
-synonym: "DiMethyl-C13HD2" RELATED Unimod-description []
-synonym: "Dimethyl:2H(4)13C(2)" RELATED PSI-MS-label []
-property_value: DiffAvg "34.06" xsd:float
-property_value: DiffFormula "(13)C 2 (2)H 4" xsd:string
-property_value: DiffMono "34.063117" xsd:float
-property_value: Formula "(12)C 6 (13)C 2 (1)H 12 (2)H 4 N 2 O 1" xsd:string
-property_value: MassAvg "162.16" xsd:float
-property_value: MassMono "162.158080" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:510
-is_a: MOD:00912
-is_a: MOD:00927
-relationship: derives_from MOD:00084
-
-[Term]
-id: MOD:01358
-name: Bruker Daltonics SERVA-ICPL(TM) quantification chemistry, medium form - site N-term
-def: "modification from Unimod Isotopic label - Use when labelling post-digest" [PubMed:15602776, Unimod:687#N-term]
-synonym: "Bruker Daltonics SERVA-ICPL(TM) quantification chemistry, medium form" RELATED Unimod-description []
-synonym: "ICPL:2H(4)" RELATED PSI-MS-label []
-property_value: DiffAvg "109.05" xsd:float
-property_value: DiffFormula "C 6 (1)H -1 (2)H 4 N 1 O 1" xsd:string
-property_value: DiffMono "109.046571" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:687
-is_a: MOD:01426
-
-[Term]
-id: MOD:01359
-name: Bruker Daltonics SERVA-ICPL(TM) quantification chemistry, medium form - site K
-def: "modification from Unimod Isotopic label - Use when labelling post-digest" [PubMed:15602776, Unimod:687#K]
-synonym: "Bruker Daltonics SERVA-ICPL(TM) quantification chemistry, medium form" RELATED Unimod-description []
-synonym: "ICPL:2H(4)" RELATED PSI-MS-label []
-property_value: DiffAvg "109.05" xsd:float
-property_value: DiffFormula "C 6 (1)H -1 (2)H 4 N 1 O 1" xsd:string
-property_value: DiffMono "109.046571" xsd:float
-property_value: Formula "C 12 (1)H 11 (2)H 4 N 3 O 2" xsd:string
-property_value: MassAvg "237.14" xsd:float
-property_value: MassMono "237.141534" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:687
-is_a: MOD:00912
-is_a: MOD:01426
-
-[Term]
-id: MOD:01360
-name: 4-sulfophenyl isothiocyanate N6-derivatized lysine
-def: "A protein modification that effectively converts an L-lysine residue to the 4-sulfophenyl isothiocyanate adduct, N6-[(4-sulfophenyl)carbamothioyl]lysine." [PubMed:14689565, PubMed:14745769, PubMed:15549660, PubMed:16526082, Unimod:261#K]
-synonym: "4-sulfophenyl isothiocyanate" RELATED Unimod-description []
-synonym: "N6-[(4-sulfophenyl)carbamothioyl]lysine" EXACT PSI-MOD-alternate []
-synonym: "SPITC" RELATED PSI-MS-label []
-property_value: DiffAvg "215.24" xsd:float
-property_value: DiffFormula "C 7 H 5 N 1 O 3 S 2" xsd:string
-property_value: DiffMono "214.971085" xsd:float
-property_value: Formula "C 13 H 17 N 3 O 4 S 2" xsd:string
-property_value: MassAvg "343.42" xsd:float
-property_value: MassMono "343.066048" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:261
-is_a: MOD:00584
-is_a: MOD:00912
-
-[Term]
-id: MOD:01361
-name: O-thiophospho-L-threonine
-def: "A protein modification that effectively converts an L-threonine residue to O-thiophospho-L-threonine." [PubMed:11507762, PubMed:12110917, Unimod:260#T]
-synonym: "Thiophospho" RELATED PSI-MS-label []
-synonym: "Thiophosphorylation" RELATED Unimod-description []
-property_value: DiffAvg "96.04" xsd:float
-property_value: DiffFormula "H 1 O 2 P 1 S 1" xsd:string
-property_value: DiffMono "95.943487" xsd:float
-property_value: Formula "C 4 H 8 N 1 O 4 P 1 S 1" xsd:string
-property_value: MassAvg "197.14" xsd:float
-property_value: MassMono "196.991165" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:260
-is_a: MOD:00583
-is_a: MOD:00917
-
-[Term]
-id: MOD:01362
-name: O-thiophospho-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O-thiophospho-L-serine." [PubMed:11507762, PubMed:12110917, Unimod:260#S]
-synonym: "Thiophospho" RELATED PSI-MS-label []
-synonym: "Thiophosphorylation" RELATED Unimod-description []
-property_value: DiffAvg "96.04" xsd:float
-property_value: DiffFormula "H 1 O 2 P 1 S 1" xsd:string
-property_value: DiffMono "95.943487" xsd:float
-property_value: Formula "C 3 H 6 N 1 O 4 P 1 S 1" xsd:string
-property_value: MassAvg "183.12" xsd:float
-property_value: MassMono "182.975515" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:260
-is_a: MOD:00583
-is_a: MOD:00916
-
-[Term]
-id: MOD:01363
-name: O4'-thiophospho-L-tyrosine
-def: "A protein modification that effectively converts an L-tyrosine residue to O4'-thiophospho-L-tyrosine." [PubMed:12110917, PubMed:15549660, Unimod:260#Y]
-synonym: "Thiophospho" RELATED PSI-MS-label []
-synonym: "Thiophosphorylation" RELATED Unimod-description []
-property_value: DiffAvg "96.04" xsd:float
-property_value: DiffFormula "H 1 O 2 P 1 S 1" xsd:string
-property_value: DiffMono "95.943487" xsd:float
-property_value: Formula "C 9 H 10 N 1 O 4 P 1 S 1" xsd:string
-property_value: MassAvg "259.22" xsd:float
-property_value: MassMono "259.006815" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:260
-is_a: MOD:00583
-is_a: MOD:00919
-
-[Term]
-id: MOD:01364
-name: fluorescein-5-thiosemicarbazide - site S
-def: "modification from Unimod Chemical derivative -" [PubMed:11467524, Unimod:478#S]
-synonym: "fluorescein-5-thiosemicarbazide" RELATED Unimod-description []
-synonym: "FTC" RELATED PSI-MS-label []
-property_value: DiffAvg "421.43" xsd:float
-property_value: DiffFormula "C 21 H 15 N 3 O 5 S 1" xsd:string
-property_value: DiffMono "421.073242" xsd:float
-property_value: Formula "C 24 H 20 N 4 O 7 S 1" xsd:string
-property_value: MassAvg "508.51" xsd:float
-property_value: MassMono "508.105270" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:478
-is_a: MOD:00626
-is_a: MOD:00916
-
-[Term]
-id: MOD:01365
-name: fluorescein-5-thiosemicarbazide - site C
-def: "modification from Unimod Chemical derivative -" [Unimod:478#C]
-synonym: "fluorescein-5-thiosemicarbazide" RELATED Unimod-description []
-synonym: "FTC" RELATED PSI-MS-label []
-property_value: DiffAvg "421.43" xsd:float
-property_value: DiffFormula "C 21 H 15 N 3 O 5 S 1" xsd:string
-property_value: DiffMono "421.073242" xsd:float
-property_value: Formula "C 24 H 20 N 4 O 6 S 2" xsd:string
-property_value: MassAvg "524.57" xsd:float
-property_value: MassMono "524.082426" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:478
-is_a: MOD:00626
-is_a: MOD:00905
-
-[Term]
-id: MOD:01366
-name: fluorescein-5-thiosemicarbazide - site K
-def: "modification from Unimod Chemical derivative -" [Unimod:478#K]
-synonym: "fluorescein-5-thiosemicarbazide" RELATED Unimod-description []
-synonym: "FTC" RELATED PSI-MS-label []
-property_value: DiffAvg "421.43" xsd:float
-property_value: DiffFormula "C 21 H 15 N 3 O 5 S 1" xsd:string
-property_value: DiffMono "421.073242" xsd:float
-property_value: Formula "C 27 H 27 N 5 O 6 S 1" xsd:string
-property_value: MassAvg "549.60" xsd:float
-property_value: MassMono "549.168205" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:478
-is_a: MOD:00626
-is_a: MOD:00912
-
-[Term]
-id: MOD:01367
-name: fluorescein-5-thiosemicarbazide - site P
-def: "modification from Unimod Chemical derivative -" [Unimod:478#P]
-synonym: "fluorescein-5-thiosemicarbazide" RELATED Unimod-description []
-synonym: "FTC" RELATED PSI-MS-label []
-property_value: DiffAvg "421.43" xsd:float
-property_value: DiffFormula "C 21 H 15 N 3 O 5 S 1" xsd:string
-property_value: DiffMono "421.073242" xsd:float
-property_value: Formula "C 26 H 22 N 4 O 6 S 1" xsd:string
-property_value: MassAvg "518.54" xsd:float
-property_value: MassMono "518.126005" xsd:float
-property_value: Origin "P" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:478
-is_a: MOD:00626
-is_a: MOD:00915
-
-[Term]
-id: MOD:01368
-name: fluorescein-5-thiosemicarbazide - site R
-def: "modification from Unimod Chemical derivative -" [PubMed:15525938, Unimod:478#R]
-synonym: "fluorescein-5-thiosemicarbazide" RELATED Unimod-description []
-synonym: "FTC" RELATED PSI-MS-label []
-property_value: DiffAvg "421.43" xsd:float
-property_value: DiffFormula "C 21 H 15 N 3 O 5 S 1" xsd:string
-property_value: DiffMono "421.073242" xsd:float
-property_value: Formula "C 27 H 27 N 7 O 6 S 1" xsd:string
-property_value: MassAvg "577.62" xsd:float
-property_value: MassMono "577.174353" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:478
-is_a: MOD:00626
-is_a: MOD:00902
-
-[Term]
-id: MOD:01369
-name: deamidated and methyl esterified residue
-def: "A protein modification that effectively replaces a carboxamido group with a carboxyl methyl ester group." [Unimod:528]
-subset: PSI-MOD-slim
-synonym: "Deamidation followed by a methylation" RELATED Unimod-description []
-synonym: "Methyl+Deamidated" RELATED PSI-MS-label []
-property_value: DiffAvg "15.01" xsd:float
-property_value: DiffFormula "C 1 H 1 N -1 O 1" xsd:string
-property_value: DiffMono "14.999666" xsd:float
-property_value: Origin "X" xsd:string
-xref: Unimod:528
-is_a: MOD:00393
-relationship: contains MOD:00400
-
-[Term]
-id: MOD:01370
-name: 6x(13)C,1x(15)N labeled residue
-def: "A protein modification that effectively converts a residue containing common isotopes to a 6x(13)C,1x(15)N labeled residue." [PubMed:11857757, PubMed:11999733, PubMed:12175151, Unimod:695]
-synonym: "13C(6) 15N(1) Silac label" RELATED Unimod-description []
-synonym: "Label:13C(6)15N(1)" RELATED PSI-MS-label []
-property_value: DiffAvg "7.02" xsd:float
-property_value: DiffFormula "(12)C -6 (13)C 6 (14)N -1 (15)N 1" xsd:string
-property_value: DiffMono "7.017164" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:695
-is_a: MOD:00842
-is_a: MOD:00843
-
-[Term]
-id: MOD:01371
-name: deamidation in presence of O18
-def: "OBSOLETE bcecause identical and redundant with MOD:00851. Remap to MOD:00851." [PubMed:8382902]
-synonym: "Deamidated:18O(1)" RELATED PSI-MS-label []
-synonym: "Deamidation in presence of O18" RELATED Unimod-description []
-property_value: DiffAvg "2.99" xsd:float
-property_value: DiffFormula "H -1 N -1 (18)O 1" xsd:string
-property_value: DiffMono "2.988262" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-replaced_by: MOD:00851
-is_obsolete: true
-
-[Term]
-id: MOD:01372
-name: (2S)-4-hydroxyleucine
-def: "A protein modification that effectively converts an L-leucine residue to a (2S)-4-hydroxyleucine." [PubMed:363352, PubMed:9164839, RESID:AA0442, ChEBI:141825]
-synonym: "(2S)-2-amino-4-hydroxy-4-methylpentanoic acid" EXACT RESID-systematic []
-synonym: "(2S)-4-hydroxyleucine" EXACT RESID-name []
-synonym: "gamma-hydroxyleucine" EXACT RESID-alternate []
-synonym: "MOD_RES (2S)-4-hydroxyleucine" EXACT UniProt-feature []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 6 H 11 N 1 O 2" xsd:string
-property_value: MassAvg "129.16" xsd:float
-property_value: MassMono "129.078979" xsd:float
-property_value: Origin "L" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0665
-is_a: MOD:01411
-
-[Term]
-id: MOD:01373
-name: (2S,4R)-5-hydroxyleucine
-def: "A protein modification that effectively converts an L-leucine residue to a (2S,4R)-5-hydroxyleucine." [PubMed:16858410, PubMed:7690768, PubMed:9164839, RESID:AA0443, ChEBI:141824]
-synonym: "(2S,4R)-2-amino-5-hydroxy-4-methylpentanoic acid" EXACT RESID-systematic []
-synonym: "(2S,4R)-5-hydroxyleucine" EXACT RESID-name []
-synonym: "(4R)-5-hydroxyleucine" EXACT RESID-alternate []
-synonym: "delta-hydroxyleucine" EXACT RESID-alternate []
-synonym: "MOD_RES (4R)-5-hydroxyleucine" EXACT UniProt-feature []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 6 H 11 N 1 O 2" xsd:string
-property_value: MassAvg "129.16" xsd:float
-property_value: MassMono "129.078979" xsd:float
-property_value: Origin "L" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: uniprot.ptm:PTM-0491
-is_a: MOD:01411
-
-[Term]
-id: MOD:01374
-name: (2S,4R)-5-oxoleucine
-def: "A modification that effectively oxygenates C5 of an L-leucine residue to form a (2S,4R)-5-oxoleucine." [ChEBI:43739, PubMed:16858410, RESID:AA0444]
-synonym: "(2S,4R)-2-amino-4-methyl-5-oxopentanoic acid" EXACT RESID-systematic []
-synonym: "(2S,4R)-5-oxoleucine" EXACT RESID-name []
-synonym: "(4R)-5-oxo-L-leucine" EXACT RESID-alternate []
-property_value: DiffAvg "13.98" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 1" xsd:string
-property_value: DiffMono "13.979265" xsd:float
-property_value: Formula "C 6 H 9 N 1 O 2" xsd:string
-property_value: MassAvg "127.14" xsd:float
-property_value: MassMono "127.063329" xsd:float
-property_value: Origin "L" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: uniprot.ptm:PTM-0492
-is_a: MOD:00679
-is_a: MOD:00911
-
-[Term]
-id: MOD:01375
-name: (2S,4R)-4,5-dihydroxyleucine
-def: "A protein modification that effectively converts an L-leucine residue to a (2S,4R)-4,5-dihydroxyleucine." [PubMed:6010785, PubMed:6893271, RESID:AA0445, ChEBI:141823]
-synonym: "(2S,4R)-2-amino-4,5-dihydroxy-4-methylpentanoic acid" EXACT RESID-systematic []
-synonym: "(2S,4R)-4,5-dihydroxyleucine" EXACT RESID-name []
-synonym: "(4R)-4,5-dihydroxyleucine" EXACT RESID-alternate []
-synonym: "gamma,delta-dihydroxyleucine" EXACT RESID-alternate []
-synonym: "MOD_RES (4R)-4,5-dihydroxyleucine" EXACT UniProt-feature []
-property_value: DiffAvg "32.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 2" xsd:string
-property_value: DiffMono "31.989829" xsd:float
-property_value: Formula "C 6 H 11 N 1 O 3" xsd:string
-property_value: MassAvg "145.16" xsd:float
-property_value: MassMono "145.073893" xsd:float
-property_value: Origin "L" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0340
-is_a: MOD:01412
-
-[Term]
-id: MOD:01376
-name: (2S,3S,4R)-3,4-dihydroxyisoleucine
-def: "A protein modification that effectively converts an L-isoleucine residue to a (2S,3S,4R)-3,4-dihydroxyisoleucine." [PubMed:11320328, RESID:AA0447, ChEBI:141827]
-synonym: "(2S,3S,4R)-2-amino-3,4-dihydroxy-3-methylpentanoic acid" EXACT RESID-systematic []
-synonym: "(2S,3S,4R)-3,4-dihydroxyisoleucine" EXACT RESID-name []
-synonym: "(3S,4R)-3,4-dihydroxyisoleucine" EXACT RESID-alternate []
-synonym: "beta,gamma-dihydroxyisoleucine" EXACT RESID-alternate []
-synonym: "MOD_RES (3S,4R)-3,4-dihydroxyisoleucine" EXACT UniProt-feature []
-property_value: DiffAvg "32.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 2" xsd:string
-property_value: DiffMono "31.989829" xsd:float
-property_value: Formula "C 6 H 11 N 1 O 3" xsd:string
-property_value: MassAvg "145.16" xsd:float
-property_value: MassMono "145.073893" xsd:float
-property_value: Origin "I" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0343
-is_a: MOD:01416
-
-[Term]
-id: MOD:01377
-name: (2S,3R,4S)-4-hydroxyisoleucine
-def: "A protein modification that effectively converts an L-isoleucine residue to a (2S,3R,4S)-4-hydroxyisoleucine." [PubMed:363352, RESID:AA0448, ChEBI:141844]
-synonym: "(2S,3R,4S)-2-amino-3-methyl-4-hydroxyvaleric acid" EXACT RESID-alternate []
-synonym: "(2S,3R,4S)-2-amino-4-hydroxy-3-methylpentanoic acid" EXACT RESID-systematic []
-synonym: "(2S,3R,4S)-4-hydroxyisoleucine" EXACT RESID-name []
-synonym: "(3R,4S)-4-hydroxyisoleucine" EXACT RESID-alternate []
-synonym: "gamma-hydroxyisoleucine" EXACT RESID-alternate []
-synonym: "MOD_RES (3R,4S)-4-hydroxyisoleucine" EXACT UniProt-feature []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 6 H 11 N 1 O 2" xsd:string
-property_value: MassAvg "129.16" xsd:float
-property_value: MassMono "129.078979" xsd:float
-property_value: Origin "I" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0337
-is_a: MOD:01415
-
-[Term]
-id: MOD:01378
-name: (2S,3R,4R)-4,5-dihydroxyisoleucine
-def: "A protein modification that effectively converts an L-isoleucine residue to a (2S,3R,4R)-4,5-dihydroxyisoleucine." [PubMed:11805306, PubMed:18552824, PubMed:363352, RESID:AA0449, ChEBI:141826]
-synonym: "(2S,3R,4R)-2-amino-4,5-dihydroxy-3-methylpentanoic acid" EXACT RESID-systematic []
-synonym: "(2S,3R,4R)-4,5-dihydroxyisoleucine" EXACT RESID-name []
-synonym: "(3R,4R)-4,5-dihydroxyisoleucine" EXACT RESID-alternate []
-synonym: "gamma,delta-dihydroxyisoleucine" EXACT RESID-alternate []
-synonym: "MOD_RES (3R,4R)-4,5-dihydroxyisoleucine" EXACT UniProt-feature []
-property_value: DiffAvg "32.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 2" xsd:string
-property_value: DiffMono "31.989829" xsd:float
-property_value: Formula "C 6 H 11 N 1 O 3" xsd:string
-property_value: MassAvg "145.16" xsd:float
-property_value: MassMono "145.073893" xsd:float
-property_value: Origin "I" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0336
-is_a: MOD:01416
-
-[Term]
-id: MOD:01379
-name: 2'-methylsulfonyl-L-tryptophan
-def: "A protein modification that effectively converts an L-tryptophan residue to 2'-methylsulfonyl-L-tryptophan." [PubMed:6893271, RESID:AA0450]
-synonym: "2'-methylsulfonyl-L-tryptophan" EXACT RESID-name []
-synonym: "2-methylsulfonyl-3-((2S)-2-amino-2-carboxyethyl)-1H-indole" EXACT RESID-systematic []
-synonym: "MOD_RES 2'-methylsulfonyltryptophan" EXACT UniProt-feature []
-property_value: DiffAvg "78.09" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 2 S 1" xsd:string
-property_value: DiffMono "77.977550" xsd:float
-property_value: Formula "C 12 H 12 N 2 O 3 S 1" xsd:string
-property_value: MassAvg "264.30" xsd:float
-property_value: MassMono "264.056863" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0304
-is_a: MOD:00918
-
-[Term]
-id: MOD:01380
-name: 2'-(S-L-cysteinyl)-6'-hydroxy-L-tryptophan sulfoxide
-def: "A protein modification that effectively cross-links an L-cysteine residue and an L-tryptophan residue by a thioether bond to form 2'-(S-L-cysteinyl)-6'-hydroxy-L-tryptophan sulfoxide." [PubMed:11805306, PubMed:18552824, PubMed:363352, PubMed:4865716, RESID:AA0451]
-comment: Cross-link 2.
-synonym: "2'-(S-L-cysteinyl)-6'-hydroxy-L-tryptophan sulfoxide" EXACT RESID-name []
-synonym: "2-((2R)-2-amino-2carboxyethyl)sulfinyl-3-((2S)-2-amino-2-carboxyethyl)-1H-indole" EXACT RESID-systematic []
-synonym: "6'-hydroxy-S-oxo-tryptathionine" EXACT RESID-alternate []
-synonym: "CROSSLNK 2'-cysteinyl-6'-hydroxytryptophan sulfoxide (Trp-Cys)" EXACT UniProt-feature []
-property_value: DiffAvg "29.98" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 2 S 0" xsd:string
-property_value: DiffMono "29.974179" xsd:float
-property_value: Formula "C 14 H 13 N 3 O 4 S 1" xsd:string
-property_value: MassAvg "319.33" xsd:float
-property_value: MassMono "319.062677" xsd:float
-property_value: Origin "C, W" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0338
-is_a: MOD:00687
-is_a: MOD:02057
-
-[Term]
-id: MOD:01381
-name: O-palmitoleyl-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O-palmitoleyl-L-serine." [OMSSA:186, PubMed:17141155, RESID:AA0455]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-((9Z)-9-hexadecenoyloxy)propanoic acid" EXACT RESID-systematic []
-synonym: "L-serine cis-9-hexadecenoate ester" EXACT RESID-alternate []
-synonym: "LIPID O-palmitoleyl serine" EXACT UniProt-feature []
-synonym: "mod186" EXACT OMSSA-label []
-synonym: "O-palmitoleyl-L-serine" EXACT RESID-name []
-synonym: "O3-palmitoleyl-serine" EXACT RESID-alternate []
-property_value: DiffAvg "236.40" xsd:float
-property_value: DiffFormula "C 16 H 28 N 0 O 1" xsd:string
-property_value: DiffMono "236.214016" xsd:float
-property_value: Formula "C 19 H 33 N 1 O 3" xsd:string
-property_value: MassAvg "323.48" xsd:float
-property_value: MassMono "323.246044" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0493
-is_a: MOD:02003
-is_a: MOD:01768
-
-[Term]
-id: MOD:01382
-name: N,N,N-trimethyl-L-methionine
-def: "A protein modification that effectively converts an L-methionine residue to N,N,N-trimethyl-L-methionine." [PubMed:18611379, RESID:AA0456]
-subset: PSI-MOD-slim
-synonym: "(1S)-1-carboxy-N,N,N-trimethyl-3-(methylsulfanyl)propanaminium" EXACT RESID-systematic []
-synonym: "(1S)-1-carboxy-N,N,N-trimethyl-3-(methylsulfanyl)propanazanium" EXACT RESID-alternate []
-synonym: "2-trimethylammonio-4-(methylthio)butanoic acid" EXACT RESID-alternate []
-synonym: "MOD_RES N,N,N-trimethylmethionine" EXACT UniProt-feature []
-synonym: "N,N,N-trimethyl-L-methionine" EXACT RESID-name []
-synonym: "N,N,N-trimethylmethionine cation" EXACT RESID-alternate []
-synonym: "N,N,N-trimethylmethioninium" EXACT RESID-alternate []
-synonym: "N2Me3+Met" EXACT PSI-MOD-label []
-property_value: DiffAvg "43.09" xsd:float
-property_value: DiffFormula "C 3 H 7 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "43.054227" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 8 H 17 N 1 O 1 S 1" xsd:string
-property_value: MassAvg "175.29" xsd:float
-property_value: MassMono "175.102537" xsd:float
-property_value: Origin "M" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0503
-is_a: MOD:01463
-is_a: MOD:01698
-
-[Term]
-id: MOD:01383
-name: L-cystine S-oxide
-def: "A protein modification that effectively cross-links two L-cysteine residues and oxidizes a sulfur to form L-cystine S-oxide." [RESID:AA0457]
-comment: Cross-link 2.
-synonym: "(2R)-2-amino-3-[([(2R)-2-amino-2-carboxyethyl]sulfanyl)sulfinyl]propanoic acid" EXACT RESID-systematic []
-synonym: "CROSSLNK S-cysteinyl 3-(oxidosulfanyl)alanine (Cys-Cys)" EXACT UniProt-feature []
-synonym: "cystine sulfoxide" EXACT RESID-alternate []
-synonym: "L-cystine S-oxide" EXACT RESID-name []
-synonym: "S-[(2R)-2-amino-3-oxopropyl] (2R)-2-amino-3-oxopropane-1-sulfinothioate" EXACT RESID-alternate []
-synonym: "S-cysteinyl 3-(oxidosulfanyl)alanine" EXACT RESID-alternate []
-property_value: DiffAvg "13.98" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 1 S 0" xsd:string
-property_value: DiffMono "13.979265" xsd:float
-property_value: Formula "C 6 H 8 N 2 O 3 S 2" xsd:string
-property_value: MassAvg "220.26" xsd:float
-property_value: MassMono "219.997634" xsd:float
-property_value: Origin "C, C" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: uniprot.ptm:PTM-0324
-is_a: MOD:02044
-is_a: MOD:00689
-
-[Term]
-id: MOD:01384
-name: aminomalonic acid (Ser)
-def: "A protein modification that effectively converts an L-serine residue to an aminomalonic acid." [PubMed:1621954, PubMed:5415959, PubMed:6366787, PubMed:7457858, RESID:AA0458]
-synonym: "2-carboxyglycine" EXACT RESID-alternate []
-synonym: "Ama" EXACT RESID-alternate []
-synonym: "aminomalonic acid" EXACT RESID-name []
-synonym: "aminopropanedioic acid" EXACT RESID-systematic []
-synonym: "MOD_RES Aminomalonic acid (Ser)" EXACT UniProt-feature []
-property_value: DiffAvg "13.98" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 1 S 0" xsd:string
-property_value: DiffMono "13.979265" xsd:float
-property_value: Formula "C 3 H 3 N 1 O 3" xsd:string
-property_value: MassAvg "101.06" xsd:float
-property_value: MassMono "101.011293" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: uniprot.ptm:PTM-0321
-is_a: MOD:00916
-
-[Term]
-id: MOD:01385
-name: 3-hydroxy-L-phenylalanine
-def: "A protein modification that effectively converts an L-phenylalanine residue to 3-hydroxy-L-phenylalanine." [ChEBI:16795, OMSSA:63, PubMed:10625477, PubMed:15651011, PubMed:16734421, PubMed:1880060, PubMed:7398618, PubMed:7844053, RESID:AA0462]
-synonym: "(2S,3S)-2-amino-3-hydroxy-3-phenylpropanoic acid" EXACT RESID-systematic []
-synonym: "3-hydoxyphenylalanine" EXACT RESID-alternate []
-synonym: "3-hydroxy-L-phenylalanine" EXACT RESID-name []
-synonym: "3-phenyl-L-serine" EXACT RESID-alternate []
-synonym: "3HyPhe" EXACT PSI-MOD-label []
-synonym: "beta-hydroxyphenylalanine" EXACT RESID-alternate []
-synonym: "beta-phenylserine" EXACT RESID-alternate []
-synonym: "hydroxylationf" EXACT OMSSA-label []
-synonym: "L-threo-3-phenylserine" EXACT RESID-alternate []
-synonym: "MOD_RES 3-hydroxyphenylalanine" EXACT UniProt-feature []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 9 H 9 N 1 O 2" xsd:string
-property_value: MassAvg "163.18" xsd:float
-property_value: MassMono "163.063329" xsd:float
-property_value: Origin "F" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0346
-is_a: MOD:00677
-is_a: MOD:00914
-
-[Term]
-id: MOD:01386
-name: 3-hydroxy-L-valine
-def: "A protein modification that effectively converts an L-valine residue to 3-hydroxy-L-valine." [PubMed:7328054, RESID:AA0463, ChEBI:141793]
-synonym: "(2S)-2-amino-3-hydroxy-3-methylbutanoic acid" EXACT RESID-systematic []
-synonym: "3-hydroxy-L-valine" EXACT RESID-name []
-synonym: "3-hydroxyvaline" EXACT RESID-alternate []
-synonym: "3HyVal" EXACT PSI-MOD-label []
-synonym: "MOD_RES 3-hydroxyvaline" EXACT UniProt-feature []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 5 H 9 N 1 O 2" xsd:string
-property_value: MassAvg "115.13" xsd:float
-property_value: MassMono "115.063329" xsd:float
-property_value: Origin "V" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0347
-is_a: MOD:00677
-is_a: MOD:00920
-
-[Term]
-id: MOD:01387
-name: O-methyl-L-threonine
-def: "A protein modification that effectively converts an L-threonine residue to O-methyl-L-threonine." [PubMed:7328054, RESID:AA0464]
-synonym: "(2S,3R)-2-amino-3-methoxybutanoic acid" EXACT RESID-systematic []
-synonym: "MOD_RES O-methylthreonine" EXACT UniProt-feature []
-synonym: "O-methyl threonine" EXACT RESID-alternate []
-synonym: "O-methyl-L-threonine" EXACT RESID-name []
-synonym: "OMeThr" EXACT PSI-MOD-label []
-synonym: "threonine methyl ether" EXACT RESID-alternate []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 5 H 9 N 1 O 2" xsd:string
-property_value: MassAvg "115.13" xsd:float
-property_value: MassMono "115.063329" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0356
-is_a: MOD:01803
-
-[Term]
-id: MOD:01388
-name: 1-amino-2-propanol
-def: "A protein modification that effectively converts an L-threonine residue into 1-amino-2-propanol." [ChEBI:15675, PubMed:7328054, RESID:AA0465]
-synonym: "(2R)-1-aminopropan-2-ol" EXACT RESID-systematic []
-synonym: "1-amino-2-hydroxypropane" EXACT RESID-alternate []
-synonym: "1-amino-2-propanol" EXACT RESID-name []
-synonym: "1-methyl-2-aminoethanol" EXACT RESID-alternate []
-synonym: "2-amino-1-methylethanol" EXACT RESID-alternate []
-synonym: "2-hydroxy-1-propylamine" EXACT RESID-alternate []
-synonym: "2-hydroxypropanamine" EXACT RESID-alternate []
-synonym: "2-hydroxypropylamine" EXACT RESID-alternate []
-synonym: "alpha-aminoisopropyl alcohol" EXACT RESID-alternate []
-synonym: "dCbxThr" EXACT PSI-MOD-label []
-synonym: "decarboxylated threonine" EXACT RESID-alternate []
-synonym: "isopropanolamine" EXACT RESID-alternate []
-synonym: "MOD_RES Decarboxylated threonine" EXACT UniProt-feature []
-synonym: "threamine" EXACT RESID-alternate []
-property_value: DiffAvg "-44.01" xsd:float
-property_value: DiffFormula "C -1 H 0 N 0 O -2" xsd:string
-property_value: DiffMono "-43.989829" xsd:float
-property_value: Formula "C 3 H 8 N 1 O 1" xsd:string
-property_value: MassAvg "74.10" xsd:float
-property_value: MassMono "74.060589" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0354
-is_a: MOD:00917
-is_a: MOD:00960
-
-[Term]
-id: MOD:01389
-name: L-isoleucine thiazole-4-carboxylic acid
-def: "A protein modification that effectively crosslinks an L-cysteine residue and an L-isoleucine residue to form L-isoleucine thiazole-4-carboxylic acid." [PubMed:11320328, RESID:AA0466]
-comment: Cross-link 2.
-synonym: "2-[(1S,2S)-1-amino-2-methylbutyl]-1,3-thiazole-4-carboxylic acid" EXACT RESID-systematic []
-synonym: "2-[1-zanyl-2-methylbutyl]-1,3-thiazole-4-carboxylic acid" EXACT RESID-alternate []
-synonym: "CROSSLNK Thiazole-4-carboxylic acid (Ile-Cys)" EXACT UniProt-feature []
-synonym: "L-isoleucine thiazole-4-carboxylic acid" EXACT RESID-name []
-property_value: DiffAvg "-20.03" xsd:float
-property_value: DiffFormula "C 0 H -4 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-20.026215" xsd:float
-property_value: Formula "C 9 H 12 N 2 O 1 S 1" xsd:string
-property_value: MassAvg "196.27" xsd:float
-property_value: MassMono "196.067034" xsd:float
-property_value: Origin "C, I" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0361
-is_a: MOD:02049
-is_a: MOD:01420
-is_a: MOD:02082
-
-[Term]
-id: MOD:01390
-name: L-valine thiazole-4-carboxylic acid
-def: "A protein modification that effectively crosslinks an L-cysteine residue and an L-valine residue to form L-valine thiazole-4-carboxylic acid." [PubMed:7328054, RESID:AA0467]
-comment: Cross-link 2.
-synonym: "2-[(1S)-1-amino-2-methylpropyl]-1,3-thiazole-4-carboxylic acid" EXACT RESID-systematic []
-synonym: "2-[1-azanyl-2-methylpropyl]-1,3-thiazole-4-carboxylic acid" EXACT RESID-alternate []
-synonym: "CROSSLNK Thiazole-4-carboxylic acid (Val-Cys)" EXACT UniProt-feature []
-synonym: "L-valine thiazole-4-carboxylic acid" EXACT RESID-name []
-property_value: DiffAvg "-20.03" xsd:float
-property_value: DiffFormula "C 0 H -4 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-20.026215" xsd:float
-property_value: Formula "C 8 H 10 N 2 O 1 S 1" xsd:string
-property_value: MassAvg "182.24" xsd:float
-property_value: MassMono "182.051384" xsd:float
-property_value: Origin "C, V" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0365
-is_a: MOD:02059
-is_a: MOD:01420
-is_a: MOD:02082
-
-[Term]
-id: MOD:01391
-name: L-valine 5-(methoxymethyl)thiazole-4-carboxylic acid
-def: "A protein modification that effectively crosslinks an L-cysteine residue and an L-valine residue, and C-5 methoxymethylates to form L-valine 5-(methoxymethyl)thiazole-4-carboxylic acid." [PubMed:10625477, PubMed:1880060, PubMed:7844053, RESID:AA0468]
-comment: Cross-link 2.
-synonym: "2-[(1S)-1-amino-2-methylpropyl]-5-(methoxymethyl)-1,3-thiazole-4-carboxylic acid" EXACT RESID-systematic []
-synonym: "2-[1-azanyl-2-methylpropyl]-5-(methoxymethyl)-1,3-thiazole-4-carboxylic acid" EXACT RESID-alternate []
-synonym: "CROSSLNK 5-(methoxymethyl)thiazole-4-carboxylic acid (Val-Cys)" EXACT UniProt-feature []
-synonym: "L-valine 5-(methoxymethyl)thiazole-4-carboxylic acid" EXACT RESID-name []
-property_value: DiffAvg "24.02" xsd:float
-property_value: DiffFormula "C 2 H 0 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "24.000000" xsd:float
-property_value: Formula "C 10 H 14 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "226.29" xsd:float
-property_value: MassMono "226.077599" xsd:float
-property_value: Origin "C, V" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0373
-is_a: MOD:02059
-is_a: MOD:01420
-
-[Term]
-id: MOD:01392
-name: L-asparagine 5-methylthiazole-4-carboxylic acid
-def: "A protein modification that effectively crosslinks an L-cysteine residue and an L-asparagine residue, and C-4 methylates to form L-asparagine 5-methylthiazole-4-carboxylic acid." [PubMed:10625477, PubMed:1880060, PubMed:7844053, RESID:AA0469]
-comment: Cross-link 2.
-synonym: "2-[(1S)-1,3-bisazanyl-3-oxopropyl]-5-methyl-1,3-thiazole-4-carboxylic acid" EXACT RESID-alternate []
-synonym: "2-[(1S)-1,3-diamino-3-oxopropyl]-5-methyl-1,3-thiazole-4-carboxylic acid" EXACT RESID-systematic []
-synonym: "CROSSLNK 5-methylthiazole-4-carboxylic acid (Asn-Cys)" EXACT UniProt-feature []
-synonym: "L-asparagine 5-methylthiazole-4-carboxylic acid" EXACT RESID-name []
-property_value: DiffAvg "-6.00" xsd:float
-property_value: DiffFormula "C 1 H -2 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-6.010565" xsd:float
-property_value: Formula "C 8 H 9 N 3 O 2 S 1" xsd:string
-property_value: MassAvg "211.24" xsd:float
-property_value: MassMono "211.041548" xsd:float
-property_value: Origin "C, N" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0352
-is_a: MOD:02042
-is_a: MOD:01420
-relationship: derives_from MOD:00656
-
-[Term]
-id: MOD:01393
-name: L-cysteine pyridine-2,5-dicarboxylic acid
-def: "A protein modification that crosslinks two serine residues and a cysteine residue by formation of a pyridine-2,5-dicarboxylic acid." [PubMed:10625477, PubMed:1880060, PubMed:7844053, RESID:AA0470]
-comment: Cross-link 3.
-synonym: "6-[(1R)-1-amino-2-sulfanylethyl]pyridine-2,5-dicarboxylic acid" EXACT RESID-systematic []
-synonym: "L-cysteine pyridine-2,5-dicarboxylic acid" EXACT RESID-name []
-property_value: DiffAvg "-70.07" xsd:float
-property_value: DiffFormula "C 0 H -8 N -1 O -3 S 0" xsd:string
-property_value: DiffMono "-70.050418" xsd:float
-property_value: Formula "C 9 H 7 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "207.23" xsd:float
-property_value: MassMono "207.022823" xsd:float
-property_value: Origin "C, S, S" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0358
-is_a: MOD:02044
-is_a: MOD:02055
-is_a: MOD:01425
-
-[Term]
-id: MOD:01394
-name: L-cysteine 5-amino-3,4,5,6-tetrahydropyridine-2,5-dicarboxylic acid
-def: "A protein modification that crosslinks two serine residues and a cysteine residue by formation of a 5-amino-3,4,5,6-tetrahydropyridine-2,5-dicarboxylic acid." [PubMed:11320328, RESID:AA0471]
-comment: Cross-link 3.
-synonym: "(5R,6R)-5-amino-6-[(1R)-1-amino-2-sulfanylethyl]-3,4,5,6-tetrahydropyridine-2,5-dicarboxylic acid" EXACT RESID-systematic []
-synonym: "L-cysteine 5-amino-3,4,5,6-tetrahydropyridine-2,5-dicarboxylic acid" EXACT RESID-name []
-synonym: "L-cysteine 5-aminopiperideine-2,5-dicarboxylic acid" EXACT RESID-alternate []
-synonym: "CROSSLNK 5-amino-piperideine-2,5-dicarboxylic acid" RELATED UniProt-feature []
-property_value: DiffAvg "-53.04" xsd:float
-property_value: DiffFormula "C 0 H -5 N 0 O -3 S 0" xsd:string
-property_value: DiffMono "-53.023869" xsd:float
-property_value: Formula "C 9 H 11 N 3 O 2 S 1" xsd:string
-property_value: MassAvg "225.27" xsd:float
-property_value: MassMono "225.057198" xsd:float
-property_value: Origin "C, S, S" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0348
-is_a: MOD:02044
-is_a: MOD:02055
-is_a: MOD:01425
-
-[Term]
-id: MOD:01395
-name: 4-(1-hydroxyethyl)-7-isoleucino-2-(threonin-O3-ylcarbonyl)-7,8-dihydroquinolin-8-ol
-def: "A protein modification that effectively results from forming an adduct between an isoleucine residue, a threonine residue and the quinaldate compound 2-carboxy-4-(1-hydroxyethyl)--7,8-dihydroquinolin-8-ol." [PubMed:11320328, RESID:AA0472]
-comment: Cross-link 2.
-synonym: "(7R,8S)-7-[(1S,2S)-1-carboxy-2-methylbutyl]amino-2-([(1S,2R)-1-amino-1-carboxypropan-2-yl]oxy)carbonyl-8-hydroxy-4-[(1S)-1-hydroxyethyl]-7,8-dihydroquinoline" EXACT RESID-systematic []
-synonym: "4-(1-hydroxyethyl)-7-isoleucino-2-(threonin-O3-ylcarbonyl)-7,8-dihydroquinolin-8-ol" EXACT RESID-name []
-synonym: "BINDING 4-(1-hydroxyethyl)-7,8-dihydroquinolin-8-ol (covalent; via 2 links)" EXACT UniProt-feature []
-property_value: DiffAvg "215.21" xsd:float
-property_value: DiffFormula "C 12 H 9 N 1 O 3" xsd:string
-property_value: DiffMono "215.058243" xsd:float
-property_value: Formula "C 22 H 28 N 3 O 6" xsd:string
-property_value: MassAvg "430.48" xsd:float
-property_value: MassMono "430.197811" xsd:float
-property_value: Origin "I, T" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:02049
-is_a: MOD:02056
-is_a: MOD:01424
-
-[Term]
-id: MOD:01396
-name: 5-hydroxy-3-methyl-L-proline (Pro)
-def: "A protein modification that effectively converts an L-proline residue to a 5-hydroxy-3-methyl-L-proline." [PubMed:7592021, PubMed:8557573, RESID:AA0473]
-comment: This entry is for the hypothetical formation of 5-hydroxy-3-methyl-L-proline from proline. For the natural production from L-isoleucine, use MOD:01897 [JSG].
-synonym: "(2S,3S,5Xi)-5-hydroxy-3-methylpyrrolidine-2-carboxylic acid" EXACT RESID-systematic []
-synonym: "5-hydroxy-3-methyl-L-proline" EXACT RESID-name []
-synonym: "5-hydroxy-3-methylproline" EXACT RESID-alternate []
-synonym: "5Hy3MePro" EXACT PSI-MOD-label []
-synonym: "beta-methyl-delta-hydroxyproline" EXACT RESID-alternate []
-synonym: "MOD_RES 5-hydroxy-3-methylproline (Ile)" EXACT UniProt-feature []
-property_value: DiffAvg "30.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 1" xsd:string
-property_value: DiffMono "30.010565" xsd:float
-property_value: Formula "C 6 H 9 N 1 O 2" xsd:string
-property_value: MassAvg "127.14" xsd:float
-property_value: MassMono "127.063329" xsd:float
-property_value: Origin "P" xsd:string
-property_value: Source "artifactual" xsd:string
-is_a: MOD:00915
-relationship: has_functional_parent MOD:01024
-relationship: has_functional_parent MOD:01417
-
-[Term]
-id: MOD:01397
-name: L-serine 5-methyloxazole-4-carboxylic acid
-def: "A protein modification that effectively crosslinks an L-serine residue and an L-threonine residue to form L-serine 5-methyloxazole-4-carboxylic acid." [PubMed:7592021, PubMed:8557573, RESID:AA0474]
-comment: Cross-link 2.
-synonym: "2-[(1S)-1-amino-2-hydroxyethyl]-5-methyl-1,3-oxazole-4-carboxylic acid" EXACT RESID-systematic []
-synonym: "2-[1-azanyl-2-hydroxyethyl]-5-methyl-1,3-oxazole-4-carboxylic acid" EXACT RESID-alternate []
-synonym: "CROSSLNK 5-methyloxazole-4-carboxylic acid (Ser-Thr)" EXACT UniProt-feature []
-synonym: "L-serine 5-methyloxazole-4-carboxylic acid" EXACT RESID-name []
-property_value: DiffAvg "-20.03" xsd:float
-property_value: DiffFormula "C 0 H -4 N 0 O -1" xsd:string
-property_value: DiffMono "-20.026215" xsd:float
-property_value: Formula "C 7 H 8 N 2 O 3" xsd:string
-property_value: MassAvg "168.15" xsd:float
-property_value: MassMono "168.053492" xsd:float
-property_value: Origin "S, T" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0386
-is_a: MOD:02055
-is_a: MOD:01422
-is_a: MOD:02082
-
-[Term]
-id: MOD:01398
-name: N6-propanoyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-propanoyl-L-lysine." [PubMed:17267393, PubMed:17684016, PubMed:20715035, RESID:AA0475, Unimod:58#K]
-comment: The binding of histone peptides with propanoylated lysine to nuclear bromodomain proteins is non-specific and weaker than binding to the corresponding acetylated lysine peptides [JSG].
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-6-(propanoylamino)hexanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-6-propionylaminocaproic acid" EXACT RESID-alternate []
-synonym: "epsilon-propanoyl-L-lysine" EXACT RESID-alternate []
-synonym: "epsilon-propionyl-L-lysine" EXACT RESID-alternate []
-synonym: "N(zeta)-propanoyllysine" EXACT RESID-alternate []
-synonym: "N6-(1-oxopropyl)-L-lysine" EXACT RESID-alternate []
-synonym: "N6-propanoyl-L-lysine" EXACT RESID-name []
-synonym: "N6-propionyllysine" EXACT RESID-alternate []
-synonym: "MOD_RES N6-propionyllysine" EXACT UniProt-feature []
-property_value: DiffAvg "56.06" xsd:float
-property_value: DiffFormula "C 3 H 4 N 0 O 1" xsd:string
-property_value: DiffMono "56.026215" xsd:float
-property_value: Formula "C 9 H 16 N 2 O 2" xsd:string
-property_value: MassAvg "184.24" xsd:float
-property_value: MassMono "184.121178" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:58
-xref: uniprot.ptm:PTM-0642
-is_a: MOD:01155
-is_a: MOD:01875
-is_a: MOD:01894
-
-[Term]
-id: MOD:01399
-name: N6-(ADP-ribosyl)-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to an N6-(ADP-ribosyl)-L-lysine." [PubMed:18436469, RESID:AA0476]
-synonym: "(S)-2-amino-6-([adenosine 5'-(trihydrogen diphosphate) 5'->5'-ester with alpha-D-ribofuranosyl]amino)hexanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-6-(ADP-ribosyl)amino-hexanoic acid" EXACT RESID-alternate []
-synonym: "epsilon-ADP-ribosyllysine" EXACT RESID-alternate []
-synonym: "MOD_RES N6-(ADP-ribosyl)lysine" EXACT UniProt-feature []
-synonym: "N(zeta)-ADP-ribosyllysine" EXACT RESID-alternate []
-synonym: "N6-(ADP-ribosyl)-L-lysine" EXACT RESID-name []
-synonym: "N6-[alpha-D-ribofuranoside 5'->5'-ester with adenosine 5'-(trihydrogen diphosphate)]-L-lysine" EXACT RESID-alternate []
-synonym: "N6-alpha-D-ribofuranosyl-L-lysine 5'->5'-ester with adenosine 5'-(trihydrogen diphosphate)" EXACT RESID-alternate []
-property_value: DiffAvg "541.30" xsd:float
-property_value: DiffFormula "C 15 H 21 N 5 O 13 P 2" xsd:string
-property_value: DiffMono "541.061109" xsd:float
-property_value: Formula "C 21 H 33 N 7 O 14 P 2" xsd:string
-property_value: MassAvg "669.48" xsd:float
-property_value: MassMono "669.156072" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: uniprot.ptm:PTM-0355
-is_a: MOD:00752
-is_a: MOD:00912
-
-[Term]
-id: MOD:01400
-name: L-lysyl-poly(ADP-ribose)
-def: "A protein modification that effectively converts an L-lysine residue to an L-lysyl-poly(ADP-ribose)." [PubMed:6772638, RESID:AA0477]
-synonym: "L-lysyl-poly(ADP-ribose)" EXACT RESID-name []
-synonym: "MOD_RES Lysyl poly(ADP-ribose)" EXACT UniProt-feature []
-synonym: "poly[2'-adenosine 5'-(trihydrogen diphosphate) 5'->5'-ester with 1alpha-D-ribofuranosyl] (2S)-2,6-diaminohexanoate" EXACT RESID-systematic []
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-is_a: MOD:02087
-is_a: MOD:00912
-
-[Term]
-id: MOD:01401
-name: (2S,3S)-3-hydroxyasparagine
-def: "A protein modification that effectively converts an L-asparagine residue to a (2S,3S)-3-hydroxyasparagine." [ChEBI:50789, PubMed:11823643, PubMed:12042299, PubMed:12215170, PubMed:17573339, RESID:AA0478, ChEBI:138107]
-subset: PSI-MOD-slim
-synonym: "(2S,3S)-2,4-diamino-3-hydroxy-4-oxobutanoic acid" EXACT RESID-alternate []
-synonym: "(2S,3S)-2-amino-3-hydroxy-4-butanediamic acid" EXACT RESID-systematic []
-synonym: "(2S,3S)-3-hydroxyasparagine" EXACT RESID-name []
-synonym: "(3S)3HyAsn" EXACT PSI-MOD-label []
-synonym: "L-threo-beta-hydroxyasparagine" EXACT RESID-alternate []
-synonym: "MOD_RES (3S)-3-hydroxyasparagine" EXACT UniProt-feature []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 4 H 6 N 2 O 3" xsd:string
-property_value: MassAvg "130.10" xsd:float
-property_value: MassMono "130.037842" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0370
-is_a: MOD:01688
-
-[Term]
-id: MOD:01402
-name: (2S,3R,4R)-3,4-dihydroxyproline
-def: "A protein modification that effectively converts an L-proline residue to a (2S,3R,4R)-3,4-dihydroxyproline." [PubMed:6893271, RESID:AA0479, ChEBI:141805]
-synonym: "(2S,3R,4R)-3,4-dihydroxyproline" EXACT RESID-name []
-synonym: "(2S,3R,4R)-3,4-dihydroxypyrrolidine-2-carboxylic acid" EXACT RESID-systematic []
-synonym: "2,3-trans-3,4-trans-3,4-dihydroxy-L-proline" EXACT RESID-alternate []
-synonym: "2-alpha-3-beta-4-alpha-3,4-dihydroxyproline" EXACT RESID-alternate []
-synonym: "MOD_RES (3R,4R)-3,4-dihydroxyproline" EXACT UniProt-feature []
-property_value: DiffAvg "32.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 2" xsd:string
-property_value: DiffMono "31.989829" xsd:float
-property_value: Formula "C 5 H 7 N 1 O 3" xsd:string
-property_value: MassAvg "129.12" xsd:float
-property_value: MassMono "129.042593" xsd:float
-property_value: Origin "P" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0368
-is_a: MOD:00866
-
-[Term]
-id: MOD:01403
-name: (2S)-4,5,5'-trihydroxyleucine
-def: "A protein modification that effectively converts an L-leucine residue to a (2S)-4,5,5'-trihydroxyleucine." [PubMed:6893271, RESID:AA0480]
-synonym: "(2S)-2-amino-4,5-dihydroxy-4-(hydroxymethyl)pentanoic acid" EXACT RESID-systematic []
-synonym: "(2S)-4,5,5'-trihydroxyleucine" EXACT RESID-name []
-synonym: "4,5,5'-trihydroxyleucine" EXACT RESID-alternate []
-synonym: "gamma,delta,delta'-trihydroxyleucine" EXACT RESID-alternate []
-synonym: "MOD_RES 4,5,4'-trihydroxyleucine" EXACT UniProt-feature []
-property_value: DiffAvg "48.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 3" xsd:string
-property_value: DiffMono "47.984744" xsd:float
-property_value: Formula "C 6 H 11 N 1 O 4" xsd:string
-property_value: MassAvg "161.16" xsd:float
-property_value: MassMono "161.068808" xsd:float
-property_value: Origin "L" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0372
-is_a: MOD:01413
-
-[Term]
-id: MOD:01404
-name: L-asparagine thiazole-4-carboxylic acid
-def: "A protein modification that effectively crosslinks an L-cysteine residue and an L-asparagine residue to form L-asparagine thiazole-4-carboxylic acid." [PubMed:7592021, PubMed:8557573, RESID:AA0481]
-comment: Cross-link 2.
-synonym: "2-[(1S)-1,3-diamino-3-oxopropyl]-1,3-thiazole-4-carboxylic acid" EXACT RESID-systematic []
-synonym: "2-[1,3-bisazanyl-3-oxopropyl]-1,3-thiazole-4-carboxylic acid" EXACT RESID-alternate []
-synonym: "CROSSLNK Thiazole-4-carboxylic acid (Asn-Cys)" EXACT UniProt-feature []
-synonym: "L-asparagine thiazole-4-carboxylic acid" EXACT RESID-name []
-property_value: DiffAvg "-20.03" xsd:float
-property_value: DiffFormula "C 0 H -4 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-20.026215" xsd:float
-property_value: Formula "C 7 H 7 N 3 O 2 S 1" xsd:string
-property_value: MassAvg "197.21" xsd:float
-property_value: MassMono "197.025897" xsd:float
-property_value: Origin "C, N" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0359
-is_a: MOD:02042
-is_a: MOD:01420
-is_a: MOD:02082
-
-[Term]
-id: MOD:01405
-name: L-proline thiazole-4-carboxylic acid
-def: "A protein modification that effectively crosslinks an L-cysteine residue and an L-proline residue to form L-proline thiazole-4-carboxylic acid." [PubMed:7592021, PubMed:8557573, RESID:AA0482]
-comment: Cross-link 2.
-synonym: "2-[(2S)-pyrrolidin-2-yl]-1,3-thiazole-4-carboxylic acid" EXACT RESID-systematic []
-synonym: "CROSSLNK Thiazole-4-carboxylic acid (Pro-Cys)" EXACT UniProt-feature []
-synonym: "L-proline thiazole-4-carboxylic acid" EXACT RESID-name []
-property_value: DiffAvg "-20.03" xsd:float
-property_value: DiffFormula "C 0 H -4 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-20.026215" xsd:float
-property_value: Formula "C 8 H 8 N 2 O 1 S 1" xsd:string
-property_value: MassAvg "180.22" xsd:float
-property_value: MassMono "180.035734" xsd:float
-property_value: Origin "C, P" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:02054
-is_a: MOD:01420
-is_a: MOD:02082
-
-[Term]
-id: MOD:01406
-name: L-threonine thiazole-4-carboxylic acid
-def: "A protein modification that effectively crosslinks an L-cysteine residue and an L-threonine residue to form L-threonine thiazole-4-carboxylic acid." [PubMed:11320328, RESID:AA0483]
-comment: Cross-link 2.
-synonym: "2-[(1S,2R)-1-amino-2-hydroxypropyl]-1,3-thiazole-4-carboxylic acid" EXACT RESID-systematic []
-synonym: "2-[1-azanyl-2-hydroxypropyl]-1,3-thiazole-4-carboxylic acid" EXACT RESID-alternate []
-synonym: "CROSSLNK Thiazole-4-carboxylic acid (Thr-Cys)" EXACT UniProt-feature []
-synonym: "L-threonine thiazole-4-carboxylic acid" EXACT RESID-name []
-property_value: DiffAvg "-20.03" xsd:float
-property_value: DiffFormula "C 0 H -4 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-20.026215" xsd:float
-property_value: Formula "C 7 H 8 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "184.21" xsd:float
-property_value: MassMono "184.030649" xsd:float
-property_value: Origin "C, T" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0364
-is_a: MOD:02056
-is_a: MOD:01420
-is_a: MOD:02082
-
-[Term]
-id: MOD:01407
-name: L-phenylalanine thiazoline-4-carboxylic acid
-def: "A protein modification that effectively crosslinks an L-cysteine residue and an L-phenylalanine residue to form L-phenylalanine thiazoline-4-carboxylic acid." [PubMed:7592021, PubMed:8557573, RESID:AA0484]
-comment: Cross-link 2.
-synonym: "(4R)-2-[(1S)-1-amino-2-phenylethyl]-4,5-dihydro-1,3-thiazole-4-carboxylic acid" EXACT RESID-systematic []
-synonym: "2-[1-azanyl-2-phenylethyl]-4,5-dihydro-1,3-thiazole-4-carboxylic acid" EXACT RESID-alternate []
-synonym: "CROSSLNK Thiazoline-4-carboxylic acid (Phe-Cys)" EXACT UniProt-feature []
-synonym: "L-phenylalanine thiazoline-4-carboxylic acid" EXACT RESID-name []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 12 H 12 N 2 O 1 S 1" xsd:string
-property_value: MassAvg "232.30" xsd:float
-property_value: MassMono "232.067034" xsd:float
-property_value: Origin "C, F" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0366
-is_a: MOD:02053
-is_a: MOD:01420
-is_a: MOD:00954
-
-[Term]
-id: MOD:01408
-name: L-threonine thiazoline-4-carboxylic acid
-def: "A protein modification that effectively crosslinks an L-cysteine residue and an L-threonine residue to form L-threonine thiazoline-4-carboxylic acid." [PubMed:11320328, RESID:AA0485]
-comment: Cross-link 2.
-synonym: "(4S)-2-[(1S,2R)-1-amino-2-hydroxypropyl]-4,5-dihydro-1,3-thiazole-4-carboxylic acid" EXACT RESID-systematic []
-synonym: "2-[1-azanyl-2-hydroxypropyl]-4,5-dihydro-1,3-thiazole-4-carboxylic acid" EXACT RESID-alternate []
-synonym: "CROSSLNK (4S)-thiazoline-4-carboxylic acid (Thr-Cys)" EXACT UniProt-feature []
-synonym: "L-threonine (4S)-thiazoline-4-carboxylic acid" EXACT RESID-name []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 7 H 10 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "186.23" xsd:float
-property_value: MassMono "186.046299" xsd:float
-property_value: Origin "C, T" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0392
-is_a: MOD:02056
-is_a: MOD:01420
-is_a: MOD:00954
-
-[Term]
-id: MOD:01409
-name: trihydroxylated residue
-def: "A protein modification that effectively replaces three hydrogen atoms with three hydroxyl groups." [PubMed:18688235]
-synonym: "Hy3Res" EXACT PSI-MOD-label []
-property_value: DiffAvg "48.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 3" xsd:string
-property_value: DiffMono "47.984744" xsd:float
-property_value: Origin "X" xsd:string
-is_a: MOD:00677
-
-[Term]
-id: MOD:01410
-name: hydroxylated leucine
-def: "A protein modification that effectively converts an L-leucine residue to an hydroxylated leucine." [PubMed:18688235]
-synonym: "HyLeu" EXACT PSI-MOD-label []
-property_value: Origin "L" xsd:string
-is_a: MOD:00677
-is_a: MOD:00911
-
-[Term]
-id: MOD:01411
-name: monohydroxylated leucine
-def: "A protein modification that effectively converts an L-leucine residue to a monohydroxylated leucine." [PubMed:18688235]
-synonym: "Hy1Leu" EXACT PSI-MOD-label []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 6 H 11 N 1 O 2" xsd:string
-property_value: MassAvg "129.16" xsd:float
-property_value: MassMono "129.078979" xsd:float
-property_value: Origin "L" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00425
-is_a: MOD:01410
-
-[Term]
-id: MOD:01412
-name: dihydroxylated leucine
-def: "A protein modification that effectively converts an L-leucine residue to a dihydroxylated leucine." [PubMed:18688235]
-synonym: "Hy2Leu" EXACT PSI-MOD-label []
-property_value: DiffAvg "32.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 2" xsd:string
-property_value: DiffMono "31.989829" xsd:float
-property_value: Formula "C 6 H 11 N 1 O 3" xsd:string
-property_value: MassAvg "145.16" xsd:float
-property_value: MassMono "145.073893" xsd:float
-property_value: Origin "L" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00428
-is_a: MOD:01410
-
-[Term]
-id: MOD:01413
-name: trihydroxylated leucine
-def: "A protein modification that effectively converts an L-leucine residue to a trihydroxylated leucine." [PubMed:18688235]
-synonym: "Hy3Leu" EXACT PSI-MOD-label []
-property_value: DiffAvg "48.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 3" xsd:string
-property_value: DiffMono "47.984744" xsd:float
-property_value: Formula "C 6 H 11 N 1 O 4" xsd:string
-property_value: MassAvg "161.16" xsd:float
-property_value: MassMono "161.068808" xsd:float
-property_value: Origin "L" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:01409
-is_a: MOD:01410
-
-[Term]
-id: MOD:01414
-name: hydroxylated isoleucine
-def: "A protein modification that effectively converts an L-isoleucine residue to an hydroxylated isoleucine." [PubMed:18688235]
-synonym: "HyIle" EXACT PSI-MOD-label []
-property_value: Origin "I" xsd:string
-is_a: MOD:00677
-is_a: MOD:00910
-
-[Term]
-id: MOD:01415
-name: monohydroxylated isoleucine
-def: "A protein modification that effectively converts an L-isoleucine residue to a monohydroxylated isoleucine." [PubMed:18688235]
-synonym: "Hy1Ile" EXACT PSI-MOD-label []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 6 H 11 N 1 O 2" xsd:string
-property_value: MassAvg "129.16" xsd:float
-property_value: MassMono "129.078979" xsd:float
-property_value: Origin "I" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00425
-is_a: MOD:01414
-
-[Term]
-id: MOD:01416
-name: dihydroxylated isoleucine
-def: "A protein modification that effectively converts an L-isoleucine residue to a dihydroxylated isoleucine." [PubMed:18688235]
-synonym: "Hy2Ile" EXACT PSI-MOD-label []
-property_value: DiffAvg "32.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 2" xsd:string
-property_value: DiffMono "31.989829" xsd:float
-property_value: Formula "C 6 H 11 N 1 O 3" xsd:string
-property_value: MassAvg "145.16" xsd:float
-property_value: MassMono "145.073893" xsd:float
-property_value: Origin "I" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00428
-is_a: MOD:01414
-
-[Term]
-id: MOD:01417
-name: monomethylated proline
-def: "A protein modification that effectively converts an L-proline residue to a monomethylated proline." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "Me1Pro" EXACT PSI-MOD-label []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 6 H 10 N 1 O 1" xsd:string
-property_value: MassAvg "112.15" xsd:float
-property_value: MassMono "112.076239" xsd:float
-property_value: Origin "P" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00599
-is_a: MOD:00712
-
-[Term]
-id: MOD:01418
-name: methylated threonine
-def: "A protein modification that effectively converts an L-threonine residue to a methylated threonine, such as O-methyl-L-threonine." [PubMed:18688235]
-synonym: "MeThr" EXACT PSI-MOD-label []
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00427
-is_a: MOD:00917
-
-[Term]
-id: MOD:01419
-name: oxazole/oxazoline ring crosslinked residues
-def: "A protein modification that crosslinks two residues by condensation of a serine or threonine hydroxyl with the carbonyl of the preceding residue to form an oxazole or oxazoline ring, or by rearrangement and condensation of a cysteine with the carbonyl of the preceding residue to form a 1,3-oxazole-4-carbothionic acid." [PubMed:18688235]
-is_a: MOD:00690
-
-[Term]
-id: MOD:01420
-name: thiazole/thiazoline ring crosslinked residues
-def: "A protein modification that crosslinks two residues by condensation of a cysteine thiol with the carbonyl of the preceding residue to form a thiazole or thiazoline ring." [PubMed:18688235]
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00687
-is_a: MOD:00690
-
-[Term]
-id: MOD:01421
-name: oxazole/oxazoline ring crosslinked residues (Ser)
-def: "A protein modification that crosslinks two residues by condensation of a serine hydroxyl with the carbonyl of the preceding residue to form an oxazole or oxazoline ring." [PubMed:18688235]
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:02055
-is_a: MOD:01419
-
-[Term]
-id: MOD:01422
-name: oxazole/oxazoline ring crosslinked residues (Thr)
-def: "A protein modification that crosslinks two residues by condensation of a threonine hydroxyl with the carbonyl of the preceding residue to form a 5-methyloxazole or 5-methyloxazoline ring." [PubMed:18688235]
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:02056
-is_a: MOD:01419
-
-[Term]
-id: MOD:01423
-name: palmitoleylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with a palmitoleyl group." [Unimod:431]
-subset: PSI-MOD-slim
-property_value: DiffAvg "236.40" xsd:float
-property_value: DiffFormula "C 16 H 28 N 0 O 1" xsd:string
-property_value: DiffMono "236.214016" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:431
-is_a: MOD:00649
-is_a: MOD:01155
-
-[Term]
-id: MOD:01424
-name: quinaldate modified residue
-def: "A protein modification that effectively results from forming an adduct with a compound containing a quinaldate, kynurenate, or xanthurenate group." [PubMed:18688235]
-is_a: MOD:01156
-
-[Term]
-id: MOD:01425
-name: pyridinyl ring crosslinked residues
-def: "A protein modification that crosslinks three residues by formation of a pyridinyl ring, such as pyridine-2,5-dicarboxylic acid or 5-aminopiperideine-2,5-dicarboxylic acid." [PubMed:18688235]
-comment: Cross-link 3.
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00033
-
-[Term]
-id: MOD:01426
-name: isotope tagged reagent derivatized residue
-def: "A protein modification that forms an adduct with a particular isotope labeled compound used as a reagent." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:00848
-
-[Term]
-id: MOD:01427
-name: 2-aminobutanoic acid (Abu)
-def: "OBSOLETE because redundant and identical to MOD:00819. Remap to MOD:00819." [PubMed:18688235]
-synonym: "Abu" EXACT DeltaMass-label []
-property_value: Formula "C 4 H 7 N 1 O 1" xsd:string
-property_value: MassAvg "85.11" xsd:float
-property_value: MassMono "85.052764" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-replaced_by: MOD:00819
-is_obsolete: true
-
-[Term]
-id: MOD:01428
-name: (13)C isotope tagged reagent
-def: "A protein modification that forms an adduct with a (13)C labeled compound used as a reagent." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:01426
-is_a: MOD:00842
-
-[Term]
-id: MOD:01429
-name: (15)N isotope tagged reagent
-def: "A protein modification that forms an adduct with a (15)N labeled compound used as a reagent." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:01426
-is_a: MOD:00843
-
-[Term]
-id: MOD:01430
-name: (18)O isotope tagged reagent
-def: "A protein modification that forms an adduct with a (13)C labeled compound used as a reagent." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:01426
-is_a: MOD:00844
-
-[Term]
-id: MOD:01431
-name: (2)H deuterium tagged reagent
-def: "A protein modification that forms an adduct with a (2)H labeled compound used as a reagent." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:01426
-is_a: MOD:00839
-
-[Term]
-id: MOD:01432
-name: (2S,4S)-4,5-dihydroxyleucine
-def: "A protein modification that effectively converts an L-leucine residue to a (2S,4S)-4,5-dihydroxyleucine." [PubMed:3718926, RESID:AA0446, ChEBI:141819]
-synonym: "(2S,4S)-2-amino-4,5-dihydroxy-4-methylpentanoic acid" EXACT RESID-systematic []
-synonym: "(2S,4S)-4,5-dihydroxyleucine" EXACT RESID-name []
-synonym: "(4S)-4,5-dihydroxyleucine" EXACT RESID-alternate []
-synonym: "gamma,delta-dihydroxyleucine" EXACT RESID-alternate []
-synonym: "MOD_RES (4S)-4,5-dihydroxyleucine" EXACT UniProt-feature []
-property_value: DiffAvg "32.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 2" xsd:string
-property_value: DiffMono "31.989829" xsd:float
-property_value: Formula "C 6 H 11 N 1 O 3" xsd:string
-property_value: MassAvg "145.16" xsd:float
-property_value: MassMono "145.073893" xsd:float
-property_value: Origin "L" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0666
-is_a: MOD:01412
-
-[Term]
-id: MOD:01433
-name: 1-amino-2-propanone
-def: "A protein modification that effectively converts an L-threonine residue into 1-amino-2-propanone." [ChEBI:17906, PubMed:12715872, PubMed:19196969, RESID:AA0486]
-synonym: "1-amino-2-propanone" EXACT RESID-name []
-synonym: "1-aminopropan-2-one" EXACT RESID-alternate []
-synonym: "1-aminopropanone" EXACT RESID-systematic []
-synonym: "aminoacetone" EXACT RESID-alternate []
-synonym: "MOD_RES 1-amino-2-propanone" EXACT UniProt-feature []
-property_value: DiffAvg "-46.03" xsd:float
-property_value: DiffFormula "C -1 H -2 N 0 O -2" xsd:string
-property_value: DiffMono "-46.005479" xsd:float
-property_value: Formula "C 3 H 6 N 1 O 1" xsd:string
-property_value: MassAvg "72.09" xsd:float
-property_value: MassMono "72.044939" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0379
-is_a: MOD:00683
-is_a: MOD:00917
-
-[Term]
-id: MOD:01434
-name: 4-hydroxy-L-glutamic acid
-def: "A protein modification that effectively converts an L-glutamic acid residue to a 4-hydroxy-L-glutamic acid." [PubMed:893891, RESID:AA0487, ChEBI:141845]
-synonym: "(2S,4Xi)-2-amino-4-hydroxypentanedioic acid" EXACT RESID-systematic []
-synonym: "4-hydroxy-L-glutamic acid" EXACT RESID-name []
-synonym: "gamma-hydroxy glutaminic acid" EXACT RESID-alternate []
-synonym: "MOD_RES 4-hydroxyglutamate" EXACT UniProt-feature []
-synonym: "threo-4-hydroxy-L-glutamic acid" EXACT RESID-alternate []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 5 H 7 N 1 O 4" xsd:string
-property_value: MassAvg "145.11" xsd:float
-property_value: MassMono "145.037508" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0453
-is_a: MOD:00425
-is_a: MOD:00906
-
-[Term]
-id: MOD:01435
-name: 2-(cystein-S-ylcarbonyl)-3-methyl-4-(glutam-5-yloxy)methylindole
-def: "A protein modification that effectively results from forming an adduct between a cysteine residue, a glutamic acid residue and the indole compound 2-carboxy-3-methyl-4-hydroxymethyl--indole." [PubMed:893891, RESID:AA0488]
-comment: Cross-link 2.
-synonym: "2-([(1R)-1-amino-1-carboxyeth-2-yl]sulfanyl)carbonyl-3-methyl-4-([(1S)-1-amino-1-carboxy-4-oxobutan-4-yl]oxy)methyl-1H-indole" EXACT RESID-systematic []
-synonym: "2-(cystein-S-ylcarbonyl)-3-methyl-4-(glutam-5-yloxy)methylindole" EXACT RESID-name []
-synonym: "2-(cystein-S-ylcarbonyl)-4-[(glutam-5-yloxy)methyl]-3-methyl-1H-indole" EXACT RESID-alternate []
-synonym: "BINDING 3-methyl-4-hydroxymethylindole-2-carboxylic acid (covalent; via 2 links)" EXACT UniProt-feature []
-property_value: DiffAvg "169.18" xsd:float
-property_value: DiffFormula "C 11 H 7 N 1 O 1 S 0" xsd:string
-property_value: DiffMono "169.052764" xsd:float
-property_value: Formula "C 19 H 19 N 3 O 5 S 1" xsd:string
-property_value: MassAvg "401.44" xsd:float
-property_value: MassMono "401.104542" xsd:float
-property_value: Origin "C, E" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00672
-is_a: MOD:02044
-is_a: MOD:02045
-
-[Term]
-id: MOD:01436
-name: cyclo[(prolylserin)-O-yl] cysteinate (Cys)
-def: "A protein modification that effectively converts an L-cysteine residue to cyclo[(prolylserin)-O-yl] cysteinate." [PubMed:7961166, RESID:AA0489#CYS]
-synonym: "(3,6-dioxopyrrolo[4,5-a]piperazin-2-yl)methyl cysteinate" EXACT RESID-alternate []
-synonym: "[(3S,8aS)-1,4-dioxooctahydropyrrolo[1,2-a]pyrazin-3-yl]methyl (2R)-2-amino-3-sulfanylpropanoate" EXACT RESID-systematic []
-synonym: "cyclo[(prolylserin)-O-yl] cysteinate" EXACT RESID-name []
-synonym: "MOD_RES Cyclo[(prolylserin)-O-yl] cysteinate" EXACT UniProt-feature []
-property_value: DiffAvg "166.18" xsd:float
-property_value: DiffFormula "C 8 H 10 N 2 O 2 S 0" xsd:string
-property_value: DiffMono "166.074228" xsd:float
-property_value: Formula "C 11 H 16 N 3 O 4 S 1" xsd:string
-property_value: MassAvg "286.33" xsd:float
-property_value: MassMono "286.086152" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-is_a: MOD:01629
-
-[Term]
-id: MOD:01437
-name: cyclo[(prolylserin)-O-yl] cysteinate (Cys-Pro-Ser cross-link)
-def: "A protein modification that effectively converts an L-cysteine residue, an L-proline residue, and an L-serine residue to cyclo[(prolylserin)-O-yl] cysteinate." [PubMed:7961166, RESID:AA0489#TRI]
-comment: Cross-link 3.
-synonym: "(3,6-dioxopyrrolo[4,5-a]piperazin-2-yl)methyl cysteinate" EXACT RESID-alternate []
-synonym: "[(3S,8aS)-1,4-dioxooctahydropyrrolo[1,2-a]pyrazin-3-yl]methyl (2R)-2-amino-3-sulfanylpropanoate" EXACT RESID-systematic []
-synonym: "cyclo[(prolylserin)-O-yl] cysteinate" EXACT RESID-name []
-synonym: "MOD_RES Cyclo[(prolylserin)-O-yl] cysteinate" EXACT UniProt-feature []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 11 H 16 N 3 O 4 S 1" xsd:string
-property_value: MassAvg "286.33" xsd:float
-property_value: MassMono "286.086152" xsd:float
-property_value: Origin "C, P, S" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0380
-is_a: MOD:02054
-is_a: MOD:02055
-is_a: MOD:01629
-is_a: MOD:00954
-
-[Term]
-id: MOD:01438
-name: S-[2-(pyridin-2-yl)ethyl]-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-[2-(pyridin-2-yl)ethyl]-L-cysteine." [PubMed:18369855, PubMed:18688235]
-comment: From DeltaMass: (name misspelled \"Pyridylethyl Cystenyl\", and formula incorrect, N and O reversed) Formula: C10H12O2N1S1 Monoisotopic Mass Change: 208.067 Average Mass Change: 208.286
-synonym: "2-PEC" EXACT PSI-MOD-alternate []
-synonym: "2-vinylpyridine derivatized cysteine residue" EXACT PSI-MOD-alternate []
-synonym: "Pyridylethyl" RELATED PSI-MS-label []
-synonym: "Pyridylethyl Cystenyl" EXACT DeltaMass-label []
-synonym: "S-(pyridin-2-ylethyl)-L-cysteine" EXACT PSI-MOD-alternate []
-synonym: "S-pyridylethylation" RELATED Unimod-description []
-property_value: DiffAvg "105.14" xsd:float
-property_value: DiffFormula "C 7 H 7 N 1" xsd:string
-property_value: DiffMono "105.057849" xsd:float
-property_value: Formula "C 10 H 12 N 2 O 1 S 1" xsd:string
-property_value: MassAvg "208.28" xsd:float
-property_value: MassMono "208.067034" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00424
-
-[Term]
-id: MOD:01439
-name: S-[2-(pyridin-4-yl)ethyl]-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-[2-(pyridin-4-yl)ethyl]-L-cysteine." [PubMed:18688235, PubMed:6528972]
-synonym: "4-PEC" EXACT PSI-MOD-alternate []
-synonym: "Pyridylethyl" RELATED PSI-MS-label []
-synonym: "Pyridylethyl Cystenyl" EXACT DeltaMass-label []
-synonym: "S-(pyridin-4-ylethyl)-L-cysteine" EXACT PSI-MOD-alternate []
-synonym: "S-pyridylethylation" RELATED Unimod-description []
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00424
-
-[Term]
-id: MOD:01440
-name: glutamyl semialdehyde
-def: "A protein modification that effectively converts a source amino acid residue to an L-glutamyl semialdehyde." [PubMed:18688235]
-synonym: "(S)-2-amino-5-oxopentanoic acid" EXACT PSI-MOD-alternate []
-synonym: "L-glutamic gamma-semialdehyde" EXACT PSI-MOD-alternate []
-property_value: Formula "C 5 H 7 N 1 O 2" xsd:string
-property_value: MassAvg "113.12" xsd:float
-property_value: MassMono "113.047678" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00859
-is_a: MOD:00594
-
-[Term]
-id: MOD:01441
-name: natural, standard, encoded residue
-def: "A protein modification that inserts or replaces a residue with a natural, standard, encoded residue." [PubMed:18688235, PubMed:6692818]
-subset: PSI-MOD-slim
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00009
-
-[Term]
-id: MOD:01442
-name: 3-(O4'-L-tyrosyl)-L-valine
-def: "A protein modification that effectively cross-links an L-valine residue and an L-tyrosine residue by an ether bond to form 3-(O4'-L-tyrosyl)-L-valine." [PubMed:19321420, RESID:AA0490]
-comment: Cross-link 2.
-synonym: "(2S)-2-amino-3-(4-[(2S)-2-amino-2-carboxyethyl]phenoxy)-3-methylbutanoic acid" EXACT RESID-systematic []
-synonym: "3-(O4'-L-tyrosyl)-L-valine" EXACT RESID-name []
-synonym: "CROSSLNK 3-(O4'-tyrosyl)-valine (Val-Tyr)" EXACT UniProt-feature []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 14 H 16 N 2 O 3" xsd:string
-property_value: MassAvg "260.29" xsd:float
-property_value: MassMono "260.116092" xsd:float
-property_value: Origin "V, Y" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0390
-is_a: MOD:00692
-is_a: MOD:02058
-is_a: MOD:02059
-
-[Term]
-id: MOD:01443
-name: tetrakis-L-glutamato bis-L-N1'-histidino lipid carboxylato manganese iron oxide
-def: "A protein modification that effectively converts four L-glutamic acid residues and two L-histidine residues to tetrakis-L-glutamato bis-L-N1'-histidino lipid carboxylato manganese iron oxide." [PubMed:19321420, RESID:AA0491]
-comment: Cross-link 6. It is not clear whether the lipid carboxylate is a cofactor or a substrate, and its identity is not certain. It was modeled as myristic acid [JSG].
-property_value: DiffAvg "350.12" xsd:float
-property_value: DiffFormula "C 14 Fe 1 H 23 Mn 1 N 0 O 3" xsd:string
-property_value: DiffMono "350.038251" xsd:float
-property_value: FormalCharge "1-" xsd:string
-property_value: Formula "C 46 Fe 1 H 65 Mn 1 N 10 O 17" xsd:string
-property_value: MassAvg "1140.86" xsd:float
-property_value: MassMono "1140.326447" xsd:float
-property_value: Origin "E, E, E, E, H, H" xsd:string
-property_value: Source "natural" xsd:string
-relationship: contains MOD:00438
-is_a: MOD:00738
-is_a: MOD:00740
-is_a: MOD:02068
-is_a: MOD:02070
-
-[Term]
-id: MOD:01444
-name: L-3,3-dihydroxyoalanine (Cys)
-def: "A protein modification that effectively converts an L-cysteine residue to L-3,3-dihydroxyoalanine." [PubMed:11435113, PubMed:17558559, RESID:AA0492#CYS]
-synonym: "(S)-2-amino-3,3-dihydroxypropanoic acid" EXACT RESID-systematic []
-synonym: "2-(dihydroxymethyl)glycine" EXACT RESID-alternate []
-synonym: "3,3-dihydroxy-L-alanine" EXACT RESID-name []
-synonym: "3,3-dihydroxyalanine" EXACT RESID-alternate []
-synonym: "3-hydroxy-L-serine" EXACT RESID-alternate []
-synonym: "3-oxoalanine hydrate" EXACT RESID-alternate []
-synonym: "C(alpha)-formylglycine hydrate" RELATED RESID-misnomer []
-property_value: DiffAvg "-0.06" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 2 S -1" xsd:string
-property_value: DiffMono "0.017758" xsd:float
-property_value: Formula "C 3 H 5 N 1 O 3" xsd:string
-property_value: MassAvg "103.08" xsd:float
-property_value: MassMono "103.026943" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00905
-is_a: MOD:01448
-
-[Term]
-id: MOD:01445
-name: L-3,3-dihydroxyoalanine (Ser)
-def: "A protein modification that effectively converts an L-serine residue to L-3,3-dihydroxyoalanine." [PubMed:11435113, PubMed:17558559, RESID:AA0492#SER]
-synonym: "(S)-2-amino-3,3-dihydroxypropanoic acid" EXACT RESID-systematic []
-synonym: "2-(dihydroxymethyl)glycine" EXACT RESID-alternate []
-synonym: "3,3-dihydroxy-L-alanine" EXACT RESID-name []
-synonym: "3,3-dihydroxyalanine" EXACT RESID-alternate []
-synonym: "3-hydroxy-L-serine" EXACT RESID-alternate []
-synonym: "3-oxoalanine hydrate" EXACT RESID-alternate []
-synonym: "C(alpha)-formylglycine hydrate" RELATED RESID-misnomer []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 3 H 5 N 1 O 3" xsd:string
-property_value: MassAvg "103.08" xsd:float
-property_value: MassMono "103.026943" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00916
-is_a: MOD:01448
-
-[Term]
-id: MOD:01446
-name: N-(dihydroxymethyl)-L-methionine (fMet)
-def: "A protein modification that effectively converts an N-formyl-Lmethionine residue to N-(dihydroxymethyl)-L-methionine." [PubMed:12595263, PubMed:9159480, RESID:AA0493]
-synonym: "(2S)-2-[(dihydroxymethyl)amino]-4-(methylsulfanyl)butanoic acid" EXACT RESID-systematic []
-synonym: "N-(dihydroxymethyl)-L-methionine" EXACT RESID-name []
-synonym: "N-formyl-L-methionine hydrate" EXACT RESID-alternate []
-synonym: "N-orthoformylmethionine" EXACT RESID-alternate []
-property_value: DiffAvg "18.02" xsd:float
-property_value: DiffFormula "C 0 H 2 N 0 O 1 S 0" xsd:string
-property_value: DiffMono "18.010565" xsd:float
-property_value: Formula "C 6 H 12 N 1 O 3 S 1" xsd:string
-property_value: MassAvg "178.23" xsd:float
-property_value: MassMono "178.053789" xsd:float
-property_value: Origin "MOD:00030" xsd:string
-property_value: Source "hypothetical" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:01450
-relationship: derives_from MOD:00030
-
-[Term]
-id: MOD:01447
-name: N-(dihydroxymethyl)-L-methionine (Met)
-def: "A protein modification that effectively converts an L-methionine residue to N-(dihydroxymethyl)-L-methionine (not known as a natural, post-translational modification process)." [PubMed:12595263, PubMed:9159480, RESID:AA0493]
-comment: This entry is for the artifactual formation of N-(dihydroxymethyl)-L-methionine from methionine. For N-(dihydroxymethyl)-L-methionine derived from encoded N-formyl-L-methionine, use MOD:01446.
-synonym: "(2S)-2-[(dihydroxymethyl)amino]-4-(methylsulfanyl)butanoic acid" EXACT RESID-systematic []
-synonym: "N-(dihydroxymethyl)-L-methionine" EXACT RESID-name []
-synonym: "N-formyl-L-methionine hydrate" EXACT RESID-alternate []
-synonym: "N-orthoformylmethionine" EXACT RESID-alternate []
-property_value: DiffAvg "46.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 2 S 0" xsd:string
-property_value: DiffMono "46.005479" xsd:float
-property_value: Formula "C 6 H 12 N 1 O 3 S 1" xsd:string
-property_value: MassAvg "178.23" xsd:float
-property_value: MassMono "178.053789" xsd:float
-property_value: Origin "M" xsd:string
-property_value: Source "hypothetical" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00913
-
-[Term]
-id: MOD:01448
-name: L-3,3-dihydroxyoalanine
-def: "A protein modification that effectively converts a source amino acid residue to L-3,3-dihydroxyoalanine." [PubMed:11435113, PubMed:17558559, RESID:AA0492]
-synonym: "(S)-2-amino-3,3-dihydroxypropanoic acid" EXACT RESID-systematic []
-synonym: "2-(dihydroxymethyl)glycine" EXACT RESID-alternate []
-synonym: "3,3-dihydroxy-L-alanine" EXACT RESID-name []
-synonym: "3,3-dihydroxyalanine" EXACT RESID-alternate []
-synonym: "3-hydroxy-L-serine" EXACT RESID-alternate []
-synonym: "3-oxoalanine hydrate" EXACT RESID-alternate []
-synonym: "C(alpha)-formylglycine hydrate" RELATED RESID-misnomer []
-property_value: Formula "C 3 H 5 N 1 O 3" xsd:string
-property_value: MassAvg "103.08" xsd:float
-property_value: MassMono "103.026943" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00859
-
-[Term]
-id: MOD:01449
-name: L-3,3-dihydroxyoalanine (Oxoalanine)
-def: "A protein modification that effectively converts an L-3-oxoalanine residue to L-3,3-dihydroxyoalanine." [PubMed:11435113, PubMed:17558559, PubMed:18688235]
-property_value: DiffAvg "18.02" xsd:float
-property_value: DiffFormula "C 0 H 2 N 0 O 1" xsd:string
-property_value: DiffMono "18.010565" xsd:float
-property_value: Formula "C 3 H 5 N 1 O 3" xsd:string
-property_value: MassAvg "103.08" xsd:float
-property_value: MassMono "103.026943" xsd:float
-property_value: Origin "MOD:01169" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:01448
-relationship: derives_from MOD:01169
-
-[Term]
-id: MOD:01450
-name: modified N-formyl-L-methionine residue
-def: "A protein modification that modifies an N-formyl-L-methionine residue." [PubMed:18688235]
-property_value: Origin "MOD:00030" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:01157
-relationship: derives_from MOD:00030
-
-[Term]
-id: MOD:01451
-name: O-phospho-L-serine arising from O-phosphopantetheine-L-serine after neutral loss of pantetheine
-def: "A protein modification that converts an L-serine residue to O-phosphopantetheine-L-serine with secondary neutral loss of pantetheine resulting in O-phospho-L-serine." [PubMed:17042494, PubMed:18688235]
-comment: Phosphoserine is generated and detected after the facile elimination of pantetheine from the phosphopantetheine tertiary phosphodiester. See MOD:01452 for alternate origin.
-subset: PSI-MOD-slim
-property_value: DiffAvg "79.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 0 O 3 P 1" xsd:string
-property_value: DiffMono "79.966331" xsd:float
-property_value: Formula "C 3 H 6 N 1 O 5 P 1" xsd:string
-property_value: MassAvg "167.06" xsd:float
-property_value: MassMono "166.998359" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00916
-is_a: MOD:00431
-relationship: derives_from MOD:00159
-
-[Term]
-id: MOD:01452
-name: O-phosphopantetheine-L-serine with neutral loss of pantetheine
-def: "Covalent modification of a peptide or protein amino acid O-phosphopantetheine-L-serine with secondary neutral loss of pantetheine resulting in O-phospho-L-serine." [PubMed:17042494, PubMed:18688235]
-comment: Phosphoserine is generated and detected after the facile elimination of pantethiene from the phosphopantethiene tertiary phosphodiester. See MOD:01451 for alternate origin.
-subset: PSI-MOD-slim
-property_value: DiffAvg "-260.35" xsd:float
-property_value: DiffFormula "C -11 H -20 N -2 O -3 P 0 S -1" xsd:string
-property_value: DiffMono "-260.119464" xsd:float
-property_value: Formula "C 3 H 6 N 1 O 5 P 1" xsd:string
-property_value: MassAvg "167.06" xsd:float
-property_value: MassMono "166.998359" xsd:float
-property_value: Origin "MOD:00159" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00916
-is_a: MOD:00431
-relationship: derives_from MOD:00159
-
-[Term]
-id: MOD:01453
-name: L-glutamic acid 5-methyl ester
-def: "A protein modification that effectively converts a source amino acid residue to L-glutamate 5-methyl ester." [RESID:AA0072]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-5-methoxy-5-oxopentanoic acid" EXACT RESID-systematic []
-synonym: "(5)-methyl L-hydrogen glutamate" EXACT RESID-alternate []
-synonym: "2-aminopentanedioic acid 5-methyl ester" EXACT RESID-alternate []
-synonym: "5-methyl esterified L-glutamic acid" EXACT PSI-MOD-alternate []
-synonym: "5-methyl L-2-aminoglutarate" EXACT RESID-alternate []
-synonym: "5-methyl L-glutamate" EXACT RESID-alternate []
-synonym: "glutamic acid 5-methyl ester" EXACT RESID-alternate []
-synonym: "glutamic acid gamma-methyl ester" EXACT RESID-alternate []
-synonym: "L-glutamic acid 5-methyl ester" EXACT RESID-name []
-synonym: "O-methyl Glutamyl" EXACT DeltaMass-label []
-synonym: "O5MeGlu" EXACT PSI-MOD-label []
-property_value: Formula "C 6 H 9 N 1 O 3" xsd:string
-property_value: MassAvg "143.14" xsd:float
-property_value: MassMono "143.058243" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00393
-is_a: MOD:00599
-is_a: MOD:00713
-is_a: MOD:00859
-
-[Term]
-id: MOD:01454
-name: N-(DNA-1',2'-dideoxyribos-1'-ylidene)-L-prolinium
-def: "A protein modification that effectively crosslinks an N-terminal L-proline residue and a strand of DNA at the C-1 of a ribose, freeing the nucleotide base and forming N-(DNA-1',2'-dideoxyribos-1'-ylidene)-L-prolinium." [PubMed:10833024, PubMed:11847126, PubMed:9030608, RESID:AA0494]
-comment: This linkage is not a Schiff-base [JSG].
-synonym: "(1Z,2S)-2-carboxy-1-[(3R,4R)-3,4-dihydroxy-5-(phosphonooxy)pentylidene]pyrrolidinium" EXACT RESID-systematic []
-synonym: "DNA glycosylase proline Schiff base intermediate" RELATED RESID-misnomer []
-synonym: "N-(DNA-1',2'-dideoxyribos-1'-ylidene)-L-prolinium" EXACT RESID-name []
-property_value: FormalCharge "1+" xsd:string
-property_value: Origin "P" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00750
-is_a: MOD:00915
-
-[Term]
-id: MOD:01455
-name: O-phosphorylated residue
-def: "A protein modification that effectively replaces a residue hydroxyl or carboxyl hydrogen with a phosphono group (H2PO3 or 'phosphate')." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "OPhosRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "79.98" xsd:float
-property_value: DiffFormula "H 1 O 3 P 1" xsd:string
-property_value: DiffMono "79.966331" xsd:float
-property_value: Origin "X" xsd:string
-is_a: MOD:00696
-
-[Term]
-id: MOD:01456
-name: N-phosphorylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of a residue amino or imino group with a phosphono group (H2PO3 or 'phosphate')." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "NPhosRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "79.98" xsd:float
-property_value: DiffFormula "H 1 O 3 P 1" xsd:string
-property_value: DiffMono "79.966331" xsd:float
-property_value: Origin "X" xsd:string
-is_a: MOD:00696
-
-[Term]
-id: MOD:01457
-name: L-cysteine (Ser)
-def: "A protein modification that effectively converts an L-serine residue to L-cysteine (not known as a natural, post-translational modification process)." [PubMed:1849824, PubMed:18688235]
-synonym: "Cys(Ser)" EXACT PSI-MOD-label []
-property_value: DiffAvg "-16.06" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1 S -1" xsd:string
-property_value: DiffMono "-15.977156" xsd:float
-property_value: Formula "C 3 H 5 N 1 O 1 S 1" xsd:string
-property_value: MassAvg "103.14" xsd:float
-property_value: MassMono "103.009185" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00749
-is_a: MOD:00916
-is_a: MOD:02088
-
-[Term]
-id: MOD:01458
-name: alpha-amino acetylated residue
-def: "A protein modification that effectively replaces a residue alpha-amino- or alpha-imino-hydrogen with an acetyl group." [OMSSA:10, Unimod:1#N-term]
-subset: PSI-MOD-slim
-synonym: "N2AcRes" EXACT PSI-MOD-label []
-synonym: "ntermacetyl" EXACT OMSSA-label []
-property_value: DiffAvg "42.04" xsd:float
-property_value: DiffFormula "C 2 H 2 N 0 O 1" xsd:string
-property_value: DiffMono "42.010565" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:1
-is_a: MOD:00408
-is_a: MOD:01696
-
-[Term]
-id: MOD:01459
-name: 4x(2)H labeled alpha-dimethylamino N-terminal residue
-def: "A protein modification that effectively converts an N-terminal residue to an 4x(2)H labeled alpha-dimethylamino N-terminal residue." [OMSSA:190, PubMed:14670044, Unimod:199#N-term]
-comment: Supposed to be alpha-amino and Lys-N6 derivatized by C(2)H2O and reduction.
-subset: PSI-MOD-slim
-synonym: "DiMethyl-CHD2" RELATED Unimod-description []
-synonym: "Dimethyl:2H(4)" RELATED PSI-MS-label []
-synonym: "mod190" EXACT OMSSA-label []
-property_value: DiffAvg "32.06" xsd:float
-property_value: DiffFormula "C 2 (2)H 4" xsd:string
-property_value: DiffMono "32.056407" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:199
-is_a: MOD:00552
-
-[Term]
-id: MOD:01460
-name: alpha-amino methylated residue
-def: "A protein modification that effectively replaces a residue alpha-amino- or alpha-imino-hydrogen with a methyl group." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "N2MeRes" EXACT PSI-MOD-label []
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00602
-
-[Term]
-id: MOD:01461
-name: N-methylated alanine
-def: "A protein modification that effectively replaces an L-alanine alpha amino hydrogen with a methyl group." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: Origin "A" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00665
-is_a: MOD:01460
-
-[Term]
-id: MOD:01462
-name: N-methylated proline
-def: "A protein modification that effectively replaces an L-proline alpha imino hydrogen with a methyl group." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: Origin "P" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00712
-is_a: MOD:01460
-
-[Term]
-id: MOD:01463
-name: N-methylated methionine
-def: "A protein modification that effectively replaces an L-methionine alpha amino hydrogen with a methyl group." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: Origin "M" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00716
-is_a: MOD:01460
-
-[Term]
-id: MOD:01464
-name: protonated L-methionine (L-methioninium) residue
-def: "A protein modification that effectively converts an L-methionine residue to an L-methioninium (protonated L-methionine)." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: DiffAvg "1.01" xsd:float
-property_value: DiffFormula "C 0 H 1 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "1.007276" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 5 H 11 N 1 O 1 S 1" xsd:string
-property_value: MassAvg "133.21" xsd:float
-property_value: MassMono "133.055586" xsd:float
-property_value: Origin "M" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00913
-is_a: MOD:01700
-
-[Term]
-id: MOD:01465
-name: N,N,N-trimethyl-L-methionine (from L-methioninium)
-def: "A protein modification that effectively converts an L-methioninium (protonated L-methionine) residue to an N6,N6,N6-trimethyl-L-methionine." [PubMed:18688235]
-comment: For amino acids residues, amine trimethylation can effectively only be accomplished with an aminium, protonated primary amino, group. This process accounts only for trimethylation and not protonation. The alternative N2Me3+Met process (MOD:01382) accounts for both protonation and trimethylation.
-subset: PSI-MOD-slim
-synonym: "N2Me3Met" EXACT PSI-MOD-label []
-property_value: DiffAvg "42.08" xsd:float
-property_value: DiffFormula "C 3 H 6 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "42.046402" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 8 H 17 N 1 O 1 S 1" xsd:string
-property_value: MassAvg "175.29" xsd:float
-property_value: MassMono "175.102537" xsd:float
-property_value: Origin "MOD:001464" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:01687
-relationship: derives_from MOD:01464
-
-[Term]
-id: MOD:01466
-name: menadione quinone derivative - site C
-def: "modification from Unimod Chemical derivative" [PubMed:15939799, Unimod:302#K]
-synonym: "Menadione" RELATED Unimod-interim []
-synonym: "Menadione quinone derivative" RELATED Unimod-description []
-property_value: DiffAvg "170.17" xsd:float
-property_value: DiffFormula "C 11 H 6 O 2" xsd:string
-property_value: DiffMono "170.036779" xsd:float
-property_value: Formula "C 14 H 11 N 1 O 3 S 1" xsd:string
-property_value: MassAvg "273.31" xsd:float
-property_value: MassMono "273.045964" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:302
-is_a: MOD:00621
-is_a: MOD:00905
-
-[Term]
-id: MOD:01467
-name: menadione quinone derivative - site K
-def: "modification from Unimod Chemical derivative" [PubMed:15939799, Unimod:302#K]
-synonym: "Menadione" RELATED Unimod-interim []
-synonym: "Menadione quinone derivative" RELATED Unimod-description []
-property_value: DiffAvg "170.17" xsd:float
-property_value: DiffFormula "C 11 H 6 O 2" xsd:string
-property_value: DiffMono "170.036779" xsd:float
-property_value: Formula "C 17 H 18 N 2 O 3" xsd:string
-property_value: MassAvg "298.34" xsd:float
-property_value: MassMono "298.131742" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:302
-is_a: MOD:00621
-is_a: MOD:00912
-
-[Term]
-id: MOD:01468
-name: L-selenocysteinyl molybdenum bis(molybdopterin guanine dinucleotide) (Cys)
-def: "A protein modification that effectively converts an L-cysteine residue to L-selenocysteinyl molybdenum bis(molybdopterin guanine dinucleotide) (not known as a natural, post-translational modification process)." [PubMed:14235557, PubMed:2211698, PubMed:8052647, PubMed:9036855, RESID:AA0248#CYS, Unimod:415]
-comment: This entry is for the artifactual formation of L-selenocysteinyl molybdenum bis(molybdopterin guanine dinucleotide) from cysteine. For natural formation from L-selenocysteine, use MOD:00253.
-synonym: "2-amino-5,6-dimercapto-7-methyl-3,7,8a,9-tetrahydro-8-oxa-1,3,9,10-tetraazaanthracen-4-one guanosine dinucleotide" EXACT RESID-alternate []
-synonym: "bis[8-amino-1a,2,4a,5,6,7,10-heptahydro-2-(trihydrogen diphosphate 5'-ester with guanosine)methyl-6-oxo-3,4-disulfanyl-pteridino[6,7-5,6]pyranoato-S3,S4]-selenocysteinyl-Se-molybdenum" EXACT RESID-systematic []
-synonym: "formate dehydrogenase selenocysteine molybdenum cofactor" EXACT RESID-alternate []
-synonym: "L-selenocysteinyl molybdenum bis(molybdopterin guanine dinucleotide)" RELATED Unimod-description []
-synonym: "L-selenocysteinyl molybdenum bis(molybdopterin guanine dinucleotide)" EXACT RESID-name []
-synonym: "molybdopterin-se" RELATED Unimod-interim []
-synonym: "MolybdopterinGD+Delta:S(-1)Se(1)" RELATED PSI-MS-label []
-property_value: DiffAvg "1618.93" xsd:float
-property_value: DiffFormula "C 40 H 47 Mo 1 N 20 O 26 P 4 S 3 Se 1" xsd:string
-property_value: DiffMono "1620.930226" xsd:float
-property_value: Formula "C 43 H 52 Mo 1 N 21 O 27 P 4 S 4 Se 1" xsd:string
-property_value: MassAvg "1722.07" xsd:float
-property_value: MassMono "1723.939410" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:415
-is_a: MOD:00744
-is_a: MOD:02073
-
-[Term]
-id: MOD:01469
-name: L-selenocysteinyl tungsten bis(molybdopterin guanine dinucleotide) (Cys)
-def: "A protein modification that effectively converts an L-cysteine residue to L-selenocysteinyl tungsten bis(molybdopterin guanine dinucleotide) (not known as a natural, post-translational modification process)." [PubMed:11372198, PubMed:12220497, RESID:AA0376#CYS]
-comment: This entry is for the artifactual formation of L-selenocysteinyl tungsten bis(molybdopterin guanine dinucleotide) from cysteine. For natural formation from L-selenocysteine, use MOD:00381.
-property_value: DiffAvg "1738.88" xsd:float
-property_value: DiffFormula "C 40 H 47 N 20 O 26 P 4 S 4 Se 1 W 1" xsd:string
-property_value: DiffMono "1738.947820" xsd:float
-property_value: Formula "C 43 H 52 N 21 O 27 P 4 S 5 Se 1 W 1" xsd:string
-property_value: MassAvg "1842.02" xsd:float
-property_value: MassMono "1841.957004" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00746
-is_a: MOD:00748
-is_a: MOD:02073
-
-[Term]
-id: MOD:01470
-name: (E)-dehydrobutyrine (Thr)
-def: "A protein modification that effectively converts an L-threonine residue to (E)-dehydrobutyrine." [DeltaMass:0, PubMed:1547888, PubMed:20805503, PubMed:3769923, RESID:AA0547]
-subset: PSI-MOD-slim
-synonym: "(2E)-2-aminobut-2-enoic acid" EXACT RESID-systematic []
-synonym: "(E)-2-amino-2-butenoic acid" EXACT RESID-alternate []
-synonym: "(E)-2-aminobutenoic acid" EXACT RESID-alternate []
-synonym: "(E)-dehydrobutyrine" EXACT RESID-name []
-synonym: "(E)dHAbu" EXACT PSI-MOD-label []
-synonym: "2,3-didehydrobutyrine" EXACT RESID-alternate []
-synonym: "3-methyldehydroalanine" EXACT RESID-alternate []
-synonym: "alpha,beta-dehydroaminobutyric acid" EXACT RESID-alternate []
-synonym: "anhydrothreonine" EXACT RESID-alternate []
-synonym: "Dehydrated" RELATED Unimod-interim []
-synonym: "Dehydration" RELATED Unimod-description []
-synonym: "Dehydroamino butyric acid" EXACT DeltaMass-label []
-synonym: "Dhb" EXACT RESID-alternate []
-synonym: "methyl-dehydroalanine" EXACT RESID-alternate []
-synonym: "MOD_RES (E)-2,3-didehydrobutyrine" EXACT UniProt-feature []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 4 H 5 N 1 O 1" xsd:string
-property_value: MassAvg "83.09" xsd:float
-property_value: MassMono "83.037114" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0441
-is_a: MOD:00190
-
-[Term]
-id: MOD:01471
-name: (Z)-dehydrobutyrine (Thr)
-def: "A protein modification that effectively converts an L-threonine residue to (Z)-dehydrobutyrine." [DeltaMass:0, PubMed:1547888, PubMed:3769923, RESID:AA0182]
-subset: PSI-MOD-slim
-synonym: "(2Z)-2-aminobut-2-enoic acid" EXACT RESID-systematic []
-synonym: "(Z)-2-amino-2-butenoic acid" EXACT RESID-alternate []
-synonym: "(Z)-2-aminobutenoic acid" EXACT RESID-alternate []
-synonym: "(Z)-dehydrobutyrine" EXACT RESID-name []
-synonym: "(Z)dHAbu" EXACT PSI-MOD-label []
-synonym: "2,3-didehydrobutyrine" EXACT RESID-alternate []
-synonym: "3-methyldehydroalanine" EXACT RESID-alternate []
-synonym: "alpha,beta-dehydroaminobutyric acid" EXACT RESID-alternate []
-synonym: "anhydrothreonine" EXACT RESID-alternate []
-synonym: "Dehydrated" RELATED Unimod-interim []
-synonym: "Dehydration" RELATED Unimod-description []
-synonym: "Dehydroamino butyric acid" EXACT DeltaMass-label []
-synonym: "Dhb" EXACT RESID-alternate []
-synonym: "methyl-dehydroalanine" EXACT RESID-alternate []
-synonym: "MOD_RES (Z)-2,3-didehydrobutyrine" EXACT UniProt-feature []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 4 H 5 N 1 O 1" xsd:string
-property_value: MassAvg "83.09" xsd:float
-property_value: MassMono "83.037114" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0440
-is_a: MOD:00190
-
-[Term]
-id: MOD:01472
-name: reduced residue
-def: "A protein modification that effectively either adds neutral hydrogen atoms (proton and electron), or removes oxygen atoms from a residue with or without the addition of hydrogen atoms." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "RedRes" EXACT PSI-MOD-label []
-is_a: MOD:01156
-
-[Term]
-id: MOD:01473
-name: hydrogenated residue
-def: "A protein modification that effectively adds neutral hydrogen atoms (proton and electron) to a residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "HRes" EXACT PSI-MOD-label []
-is_a: MOD:01472
-
-[Term]
-id: MOD:01474
-name: O-[S-(carboxymethyl)phosphopantetheine]-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O-[S-(carboxymethyl)phosphopantetheine]-L-serine." [PubMed:18688235]
-comment: This modification results from the derivatization of the pantetheine sulfhydryl with iodoacetic acid [JSG].
-property_value: DiffAvg "398.37" xsd:float
-property_value: DiffFormula "C 13 H 23 N 2 O 8 P 1 S 1" xsd:string
-property_value: DiffMono "398.091273" xsd:float
-property_value: Formula "C 16 H 28 N 3 O 10 P 1 S 1" xsd:string
-property_value: MassAvg "485.44" xsd:float
-property_value: MassMono "485.123302" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-relationship: derives_from MOD:00399
-is_a: MOD:00861
-is_a: MOD:00916
-relationship: derives_from MOD:00159
-
-[Term]
-id: MOD:01475
-name: O-[S-(carboxamidomethyl)phosphopantetheine]-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O-[S-(carboxamidomethyl)phosphopantetheine]-L-serine." [PubMed:18688235]
-comment: This modification results from the derivatization of the pantetheine sulfhydryl with iodoacetamide [JSG].
-property_value: DiffAvg "397.38" xsd:float
-property_value: DiffFormula "C 13 H 24 N 3 O 7 P 1 S 1" xsd:string
-property_value: DiffMono "397.107258" xsd:float
-property_value: Formula "C 16 H 29 N 4 O 9 P 1 S 1" xsd:string
-property_value: MassAvg "484.46" xsd:float
-property_value: MassMono "484.139286" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-relationship: derives_from MOD:00397
-is_a: MOD:00861
-is_a: MOD:00916
-relationship: derives_from MOD:00159
-
-[Term]
-id: MOD:01476
-name: 2'-fluoro-L-phenylalanine
-def: "A protein modification that effectively converts an L-phenylalanine residue to an 2'-fluoro-L-fluorophenylalanine." [PubMed:18688235, PubMed:8172898]
-synonym: "2-fluorophenylalanine" EXACT PSI-MOD-alternate []
-synonym: "o-fluorophenylalanine" EXACT PSI-MOD-alternate []
-synonym: "ortho-fluorophenylalanine" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "17.99" xsd:float
-property_value: DiffFormula "C 0 F 1 H -1 N 0 O 0" xsd:string
-property_value: DiffMono "17.990578" xsd:float
-property_value: Formula "C 9 F 1 H 8 N 1 O 1" xsd:string
-property_value: MassAvg "165.17" xsd:float
-property_value: MassMono "165.058992" xsd:float
-property_value: Origin "F" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01227
-
-[Term]
-id: MOD:01477
-name: 3'-fluoro-L-phenylalanine
-def: "A protein modification that effectively converts an L-phenylalanine residue to an 3'-fluoro-L-fluorophenylalanine." [PubMed:18688235, PubMed:8172898]
-synonym: "3-fluorophenylalanine" EXACT PSI-MOD-alternate []
-synonym: "m-fluorophenylalanine" EXACT PSI-MOD-alternate []
-synonym: "meta-fluorophenylalanine" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "17.99" xsd:float
-property_value: DiffFormula "C 0 F 1 H -1 N 0 O 0" xsd:string
-property_value: DiffMono "17.990578" xsd:float
-property_value: Formula "C 9 F 1 H 8 N 1 O 1" xsd:string
-property_value: MassAvg "165.17" xsd:float
-property_value: MassMono "165.058992" xsd:float
-property_value: Origin "F" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01227
-
-[Term]
-id: MOD:01478
-name: 4'-fluoro-L-phenylalanine
-def: "A protein modification that effectively converts an L-phenylalanine residue into an 4'-fluoro-L-fluorophenylalanine." [PubMed:18688235, PubMed:8172898]
-synonym: "4-fluorophenylalanine" EXACT PSI-MOD-alternate []
-synonym: "p-fluorophenylalanine" EXACT PSI-MOD-alternate []
-synonym: "para-fluorophenylalanine" EXACT PSI-MOD-alternate []
-synonym: "rho-fluorophenylalanine" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "17.99" xsd:float
-property_value: DiffFormula "C 0 F 1 H -1 N 0 O 0" xsd:string
-property_value: DiffMono "17.990578" xsd:float
-property_value: Formula "C 9 F 1 H 8 N 1 O 1" xsd:string
-property_value: MassAvg "165.17" xsd:float
-property_value: MassMono "165.058992" xsd:float
-property_value: Origin "F" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01227
-
-[Term]
-id: MOD:01479
-name: 4'-fluoro-L-tryptophan
-def: "A protein modification that effectively converts an L-tryptophan residue into an 4'-fluoro-L-tryptophan." [PubMed:18688235, PubMed:8172898]
-synonym: "4-fluorotryptophan" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "17.99" xsd:float
-property_value: DiffFormula "F 1 H -1" xsd:string
-property_value: DiffMono "17.990578" xsd:float
-property_value: Formula "C 11 F 1 H 9 N 2 O 1" xsd:string
-property_value: MassAvg "204.20" xsd:float
-property_value: MassMono "204.069891" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01226
-
-[Term]
-id: MOD:01480
-name: 5'-fluoro-L-tryptophan
-def: "A protein modification that effectively converts an L-tryptophan residue into an 5'-fluoro-L-tryptophan." [PubMed:18688235, PubMed:8172898]
-synonym: "5-fluorotryptophan" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "17.99" xsd:float
-property_value: DiffFormula "F 1 H -1" xsd:string
-property_value: DiffMono "17.990578" xsd:float
-property_value: Formula "C 11 F 1 H 9 N 2 O 1" xsd:string
-property_value: MassAvg "204.20" xsd:float
-property_value: MassMono "204.069891" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01226
-
-[Term]
-id: MOD:01481
-name: 6'-fluoro-L-tryptophan
-def: "A protein modification that effectively converts an L-tryptophan residue into an 6'-fluoro-L-tryptophan." [PubMed:18688235, PubMed:8172898]
-synonym: "6-fluorotryptophan" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "17.99" xsd:float
-property_value: DiffFormula "F 1 H -1" xsd:string
-property_value: DiffMono "17.990578" xsd:float
-property_value: Formula "C 11 F 1 H 9 N 2 O 1" xsd:string
-property_value: MassAvg "204.20" xsd:float
-property_value: MassMono "204.069891" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01226
-
-[Term]
-id: MOD:01482
-name: calcium containing modified residue
-def: "A protein modification that effectively substitutes a calcium atom or a cluster containing calcium for hydrogen atoms, or that coordinates a calcium ion." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "CaRes" EXACT PSI-MOD-label []
-is_a: MOD:00698
-
-[Term]
-id: MOD:01483
-name: O-formylated residue
-def: "A protein modification that effectively replaces a residue hydroxyl group with a formyloxy group." [PubMed:18688235]
-synonym: "OFoRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "28.01" xsd:float
-property_value: DiffFormula "C 1 O 1" xsd:string
-property_value: DiffMono "27.994915" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00493
-is_a: MOD:00671
-
-[Term]
-id: MOD:01484
-name: N6-(L-isoglutamyl)-L-lysine (Glu)
-def: "A protein modification that effectively crosslinks an L-glutamic acid residue and an L-lysine residue by an isopeptide bond to form N6-(L-isoglutamyl)-L-lysine and the release of water." [ChEBI:21863, PubMed:19015515, RESID:AA0124#GLU]
-comment: Cross-link 2. This cross-link is usually made by glutamine and releases ammonia, rather than glutamic acid and requiring the consumption of ATP.
-synonym: "(2S)-2-amino-6-([(4S)-4-amino-4-carboxybutanoyl]amino)hexanoic acid" EXACT RESID-systematic []
-synonym: "2-azanyl-6-([4-azanyl-4-carboxybutanoyl]azanyl)hexanoic acid" EXACT RESID-alternate []
-synonym: "5-glutamyl N6-lysine" EXACT RESID-alternate []
-synonym: "N alpha -(gamma-Glutamyl)-lysine" EXACT DeltaMass-label []
-synonym: "N(epsilon)-(gamma-glutamyl)lysine" EXACT RESID-alternate []
-synonym: "N6-(L-isoglutamyl)-L-lysine" EXACT RESID-name []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 11 H 17 N 3 O 3" xsd:string
-property_value: MassAvg "239.27" xsd:float
-property_value: MassMono "239.126991" xsd:float
-property_value: Origin "K, E" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:02045
-is_a: MOD:00954
-is_a: MOD:01630
-
-[Term]
-id: MOD:01485
-name: iTRAQ4plex-114 reporter+balance reagent acylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of a residue with the Applied Biosystems iTRAQ4plex-114 reporter+balance group." [Unimod:532]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Accurate mass for 114" RELATED Unimod-description []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ114" RELATED Unimod-interim []
-synonym: "iTRAQ4plex114" RELATED PSI-MS-label []
-property_value: DiffAvg "144.11" xsd:float
-property_value: DiffFormula "(12)C 5 (13)C 2 H 12 N 2 (18)O 1" xsd:string
-property_value: DiffMono "144.105919" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:532
-is_a: MOD:01428
-is_a: MOD:01430
-is_a: MOD:01516
-is_a: MOD:01518
-
-[Term]
-id: MOD:01486
-name: iTRAQ4plex-114 reporter+balance reagent acylated N-terminal
-def: "A protein modification that effectively replaces a hydrogen atom of a protein N-terminal with the Applied Biosystems iTRAQ4plex-114 reporter+balance group." [OMSSA:167, Unimod:532#N-term]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Accurate mass for 114" RELATED Unimod-description []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ114" RELATED Unimod-interim []
-synonym: "iTRAQ114nterm" EXACT OMSSA-label []
-synonym: "iTRAQ4plex114" RELATED PSI-MS-label []
-property_value: DiffAvg "144.11" xsd:float
-property_value: DiffFormula "(12)C 5 (13)C 2 H 12 N 2 (18)O 1" xsd:string
-property_value: DiffMono "144.105919" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:532
-is_a: MOD:01485
-is_a: MOD:01711
-
-[Term]
-id: MOD:01487
-name: iTRAQ4plex-114 reporter+balance reagent N6-acylated lysine
-def: "A protein modification that effectively replaces the N6'-hydrogen atom of a lysine residue with the Applied Biosystems iTRAQ4plex-114 reporter+balance group." [OMSSA:168, Unimod:532#K]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Accurate mass for 114" RELATED Unimod-description []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ114" RELATED Unimod-interim []
-synonym: "iTRAQ114K" EXACT OMSSA-label []
-synonym: "iTRAQ4plex114" RELATED PSI-MS-label []
-property_value: DiffAvg "144.11" xsd:float
-property_value: DiffFormula "(12)C 5 (13)C 2 H 12 N 2 (18)O 1" xsd:string
-property_value: DiffMono "144.105919" xsd:float
-property_value: Formula "(12)C 11 (13)C 2 H 24 N 4 (16)O 1 (18)O 1" xsd:string
-property_value: MassAvg "272.20" xsd:float
-property_value: MassMono "272.200882" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:532
-is_a: MOD:01485
-is_a: MOD:01709
-is_a: MOD:01875
-
-[Term]
-id: MOD:01488
-name: iTRAQ4plex-114 reporter+balance reagent O4'-acylated tyrosine
-def: "A protein modification that effectively replaces the O4'-hydrogen atom of a tyrosine residue with the Applied Biosystems iTRAQ4plex-114 reporter+balance group." [OMSSA:169, Unimod:532#Y]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Accurate mass for 114" RELATED Unimod-description []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ114" RELATED Unimod-interim []
-synonym: "iTRAQ114Y" EXACT OMSSA-label []
-synonym: "iTRAQ4plex114" RELATED PSI-MS-label []
-property_value: DiffAvg "144.11" xsd:float
-property_value: DiffFormula "(12)C 5 (13)C 2 H 12 N 2 (18)O 1" xsd:string
-property_value: DiffMono "144.105919" xsd:float
-property_value: Formula "(12)C 14 (13)C 2 H 21 N 3 (16)O 2 (18)O 1" xsd:string
-property_value: MassAvg "307.17" xsd:float
-property_value: MassMono "307.169248" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:532
-is_a: MOD:00919
-is_a: MOD:01485
-is_a: MOD:01713
-
-[Term]
-id: MOD:01489
-name: iTRAQ4plex-114 reporter+balance reagent N'-acylated histidine
-def: "A protein modification that effectively replaces an N'-hydrogen atom of a histidine residue with the Applied Biosystems iTRAQ4plex-114 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "iTRAQ4plex114" RELATED PSI-MS-label []
-property_value: DiffAvg "144.11" xsd:float
-property_value: DiffFormula "(12)C 5 (13)C 2 H 12 N 2 (18)O 1" xsd:string
-property_value: DiffMono "144.105919" xsd:float
-property_value: Formula "(12)C 11 (13)C 2 H 19 N 5 O 1 (18)O 1" xsd:string
-property_value: MassAvg "281.16" xsd:float
-property_value: MassMono "281.164831" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00909
-is_a: MOD:01485
-is_a: MOD:01709
-
-[Term]
-id: MOD:01490
-name: iTRAQ4plex-114 reporter+balance reagent O3-acylated serine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a serine residue with the Applied Biosystems iTRAQ4plex-114 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "iTRAQ4plex114" RELATED PSI-MS-label []
-property_value: DiffAvg "144.11" xsd:float
-property_value: DiffFormula "(12)C 5 (13)C 2 H 12 N 2 (18)O 1" xsd:string
-property_value: DiffMono "144.105919" xsd:float
-property_value: Formula "(12)C 8 (13)C 2 H 17 N 3 O 2 (18)O 1" xsd:string
-property_value: MassAvg "231.14" xsd:float
-property_value: MassMono "231.137947" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02003
-is_a: MOD:01485
-is_a: MOD:01713
-
-[Term]
-id: MOD:01491
-name: iTRAQ4plex-114 reporter+balance reagent O3-acylated threonine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a threonine residue with the Applied Biosystems iTRAQ4plex-114 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "iTRAQ4plex114" RELATED PSI-MS-label []
-property_value: DiffAvg "144.11" xsd:float
-property_value: DiffFormula "(12)C 5 (13)C 2 H 12 N 2 (18)O 1" xsd:string
-property_value: DiffMono "144.105919" xsd:float
-property_value: Formula "(12)C 9 (13)C 2 H 19 N 3 O 2 (18)O 1" xsd:string
-property_value: MassAvg "245.15" xsd:float
-property_value: MassMono "245.153598" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02004
-is_a: MOD:01485
-is_a: MOD:01713
-
-[Term]
-id: MOD:01492
-name: iTRAQ4plex-115 reporter+balance reagent acylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of a residue with the Applied Biosystems iTRAQ4plex-115 reporter+balance group." [Unimod:533]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Accurate mass for 115" RELATED Unimod-description []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ115" RELATED Unimod-interim []
-synonym: "iTRAQ4plex115" RELATED PSI-MS-label []
-property_value: DiffAvg "144.10" xsd:float
-property_value: DiffFormula "(12)C 6 (13)C 1 H 12 (14)N 1 (15)N 1 (18)O 1" xsd:string
-property_value: DiffMono "144.099599" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:533
-is_a: MOD:01428
-is_a: MOD:01429
-is_a: MOD:01430
-is_a: MOD:01516
-is_a: MOD:01518
-
-[Term]
-id: MOD:01493
-name: iTRAQ4plex-115 reporter+balance reagent acylated N-terminal
-def: "A protein modification that effectively replaces a hydrogen atom of a protein N-terminal with the Applied Biosystems iTRAQ4plex-115 reporter+balance group." [OMSSA:170, Unimod:533#N-term]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Accurate mass for 115" RELATED Unimod-description []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ115" RELATED Unimod-interim []
-synonym: "iTRAQ115nterm" EXACT OMSSA-label []
-synonym: "iTRAQ4plex115" RELATED PSI-MS-label []
-property_value: DiffAvg "144.10" xsd:float
-property_value: DiffFormula "(12)C 6 (13)C 1 H 12 (14)N 1 (15)N 1 (18)O 1" xsd:string
-property_value: DiffMono "144.099599" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:533
-is_a: MOD:01492
-is_a: MOD:01711
-
-[Term]
-id: MOD:01494
-name: iTRAQ4plex-115 reporter+balance reagent N6-acylated lysine
-def: "A protein modification that effectively replaces the N6'-hydrogen atom of a lysine residue with the Applied Biosystems iTRAQ4plex-115 reporter+balance group." [OMSSA:171, Unimod:533#K]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Accurate mass for 115" RELATED Unimod-description []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ115" RELATED Unimod-interim []
-synonym: "iTRAQ115K" EXACT OMSSA-label []
-synonym: "iTRAQ4plex115" RELATED PSI-MS-label []
-property_value: DiffAvg "144.10" xsd:float
-property_value: DiffFormula "(12)C 6 (13)C 1 H 12 (14)N 1 (15)N 1 (18)O 1" xsd:string
-property_value: DiffMono "144.099599" xsd:float
-property_value: Formula "(12)C 12 (13)C 1 H 24 (14)N 3 (15)N 1 (16)O 1 (18)O 1" xsd:string
-property_value: MassAvg "272.19" xsd:float
-property_value: MassMono "272.194562" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:533
-is_a: MOD:01492
-is_a: MOD:01709
-is_a: MOD:01875
-
-[Term]
-id: MOD:01495
-name: iTRAQ4plex-115 reporter+balance reagent O4'-acylated tyrosine
-def: "A protein modification that effectively replaces the O4'-hydrogen atom of a tyrosine residue with the Applied Biosystems iTRAQ4plex-115 reporter+balance group." [OMSSA:172, Unimod:533#Y]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Accurate mass for 115" RELATED Unimod-description []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ115" RELATED Unimod-interim []
-synonym: "iTRAQ115Y" EXACT OMSSA-label []
-synonym: "iTRAQ4plex115" RELATED PSI-MS-label []
-property_value: DiffAvg "144.10" xsd:float
-property_value: DiffFormula "(12)C 6 (13)C 1 H 12 (14)N 1 (15)N 1 (18)O 1" xsd:string
-property_value: DiffMono "144.099599" xsd:float
-property_value: Formula "(12)C 15 (13)C 1 H 21 (14)N 2 (15)N 1 (16)O 2 (18)O 1" xsd:string
-property_value: MassAvg "307.16" xsd:float
-property_value: MassMono "307.162928" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:533
-is_a: MOD:00919
-is_a: MOD:01492
-is_a: MOD:01713
-
-[Term]
-id: MOD:01496
-name: iTRAQ4plex-115 reporter+balance reagent N'-acylated histidine
-def: "A protein modification that effectively replaces an N'-hydrogen atom of a histidine residue with the Applied Biosystems iTRAQ4plex-115 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "iTRAQ4plex115" RELATED PSI-MS-label []
-property_value: DiffAvg "144.10" xsd:float
-property_value: DiffFormula "(12)C 6 (13)C 1 H 12 (14)N 1 (15)N 1 (18)O 1" xsd:string
-property_value: DiffMono "144.099599" xsd:float
-property_value: Formula "(12)C 12 (13)C 1 H 19 (14)N 4 (15)N 1 (16)O 1 (18)O 1" xsd:string
-property_value: MassAvg "281.16" xsd:float
-property_value: MassMono "281.158511" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00909
-is_a: MOD:01492
-is_a: MOD:01709
-
-[Term]
-id: MOD:01497
-name: iTRAQ4plex-115 reporter+balance reagent O3-acylated serine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a serine residue with the Applied Biosystems iTRAQ4plex-115 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "iTRAQ4plex115" RELATED PSI-MS-label []
-property_value: DiffAvg "144.10" xsd:float
-property_value: DiffFormula "(12)C 6 (13)C 1 H 12 (14)N 1 (15)N 1 (18)O 1" xsd:string
-property_value: DiffMono "144.099599" xsd:float
-property_value: Formula "(12)C 9 (13)C 1 H 17 N 1 (14)N 1 (15)N 1 (16)O 2 (18)O 1" xsd:string
-property_value: MassAvg "231.13" xsd:float
-property_value: MassMono "231.131628" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02003
-is_a: MOD:01492
-is_a: MOD:01713
-
-[Term]
-id: MOD:01498
-name: iTRAQ4plex-115 reporter+balance reagent O3-acylated threonine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a threonine residue with the Applied Biosystems iTRAQ4plex-115 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "iTRAQ4plex115" RELATED PSI-MS-label []
-property_value: DiffAvg "144.10" xsd:float
-property_value: DiffFormula "(12)C 6 (13)C 1 H 12 (14)N 1 (15)N 1 (18)O 1" xsd:string
-property_value: DiffMono "144.099599" xsd:float
-property_value: Formula "(12)C 10 (13)C 1 H 19 (14)N 2 (15)N 1 (16)O 2 (18)O 1" xsd:string
-property_value: MassAvg "245.15" xsd:float
-property_value: MassMono "245.147278" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02004
-is_a: MOD:01492
-is_a: MOD:01713
-
-[Term]
-id: MOD:01499
-name: iTRAQ4plex-116 reporter+balance reagent acylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of a residue with the Applied Biosystems iTRAQ4plex-116 reporter+balance group." [Unimod:214]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ" RELATED Unimod-interim []
-synonym: "iTRAQ4plex" RELATED PSI-MS-label []
-synonym: "Representative mass and accurate mass for 116 & 117" RELATED Unimod-description []
-property_value: DiffAvg "144.10" xsd:float
-property_value: DiffFormula "(12)C 4 (13)C 3 H 12 (14)N 1 (15)N 1 (16)O 1" xsd:string
-property_value: DiffMono "144.102062" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:214
-is_a: MOD:01428
-is_a: MOD:01429
-is_a: MOD:01517
-is_a: MOD:01518
-
-[Term]
-id: MOD:01500
-name: iTRAQ4plex-116 reporter+balance reagent acylated N-terminal
-def: "A protein modification that effectively replaces a hydrogen atom of a protein N-terminal with the Applied Biosystems iTRAQ4plex-116 reporter+balance group." [OMSSA:173, Unimod:214#N-term]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ" RELATED Unimod-interim []
-synonym: "iTRAQ116nterm" EXACT OMSSA-label []
-synonym: "iTRAQ4plex" RELATED PSI-MS-label []
-synonym: "Representative mass and accurate mass for 116 & 117" RELATED Unimod-description []
-property_value: DiffAvg "144.10" xsd:float
-property_value: DiffFormula "(12)C 4 (13)C 3 H 12 (14)N 1 (15)N 1 (16)O 1" xsd:string
-property_value: DiffMono "144.102062" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:214
-is_a: MOD:01499
-is_a: MOD:01711
-
-[Term]
-id: MOD:01501
-name: iTRAQ4plex-116 reporter+balance reagent N6-acylated lysine
-def: "A protein modification that effectively replaces the N6'-hydrogen atom of a lysine residue with the Applied Biosystems iTRAQ4plex-116 reporter+balance group." [OMSSA:174, Unimod:214#K]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ" RELATED Unimod-interim []
-synonym: "iTRAQ116K" EXACT OMSSA-label []
-synonym: "iTRAQ4plex" RELATED PSI-MS-label []
-synonym: "Representative mass and accurate mass for 116 & 117" RELATED Unimod-description []
-property_value: DiffAvg "144.10" xsd:float
-property_value: DiffFormula "(12)C 4 (13)C 3 H 12 (14)N 1 (15)N 1 (16)O 1" xsd:string
-property_value: DiffMono "144.102062" xsd:float
-property_value: Formula "(12)C 10 (13)C 3 H 24 N 2 (14)N 1 (15)N 1 O 1 (16)O 1" xsd:string
-property_value: MassAvg "272.20" xsd:float
-property_value: MassMono "272.197025" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:214
-is_a: MOD:01499
-is_a: MOD:01709
-is_a: MOD:01875
-
-[Term]
-id: MOD:01502
-name: iTRAQ4plex-116 reporter+balance reagent O4'-acylated tyrosine
-def: "A protein modification that effectively replaces the O4'-hydrogen atom of a tyrosine residue with the Applied Biosystems iTRAQ4plex-116 reporter+balance group." [OMSSA:175, Unimod:214#Y]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ" RELATED Unimod-interim []
-synonym: "iTRAQ116Y" EXACT OMSSA-label []
-synonym: "iTRAQ4plex" RELATED PSI-MS-label []
-synonym: "Representative mass and accurate mass for 116 & 117" RELATED Unimod-description []
-property_value: DiffAvg "144.10" xsd:float
-property_value: DiffFormula "(12)C 4 (13)C 3 H 12 (14)N 1 (15)N 1 (16)O 1" xsd:string
-property_value: DiffMono "144.102062" xsd:float
-property_value: Formula "(12)C 13 (13)C 3 H 21 N 1 (14)N 1 (15)N 1 O 2 (16)O 1" xsd:string
-property_value: MassAvg "307.17" xsd:float
-property_value: MassMono "307.165391" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:214
-is_a: MOD:00919
-is_a: MOD:01499
-is_a: MOD:01713
-
-[Term]
-id: MOD:01503
-name: iTRAQ4plex-116 reporter+balance reagent N'-acylated histidine
-def: "A protein modification that effectively replaces an N'-hydrogen atom of a histidine residue with the Applied Biosystems iTRAQ4plex-116 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "iTRAQ4plex" RELATED PSI-MS-label []
-property_value: DiffAvg "144.10" xsd:float
-property_value: DiffFormula "(12)C 4 (13)C 3 H 12 (14)N 1 (15)N 1 (16)O 1" xsd:string
-property_value: DiffMono "144.102062" xsd:float
-property_value: Formula "(12)C 10 (13)C 3 H 19 N 3 (14)N 1 (15)N 1 (16)O 2" xsd:string
-property_value: MassAvg "281.16" xsd:float
-property_value: MassMono "281.160974" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00909
-is_a: MOD:01499
-is_a: MOD:01709
-
-[Term]
-id: MOD:01504
-name: iTRAQ4plex-116 reporter+balance reagent O3-acylated serine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a serine residue with the Applied Biosystems iTRAQ4plex-116 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "iTRAQ4plex" RELATED PSI-MS-label []
-property_value: DiffAvg "144.10" xsd:float
-property_value: DiffFormula "(12)C 4 (13)C 3 H 12 (14)N 1 (15)N 1 (16)O 1" xsd:string
-property_value: DiffMono "144.102062" xsd:float
-property_value: Formula "(12)C 7 (13)C 3 H 17 (14)N 2 (15)N 1 (16)O 3" xsd:string
-property_value: MassAvg "231.13" xsd:float
-property_value: MassMono "231.134091" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02003
-is_a: MOD:01499
-is_a: MOD:01713
-
-[Term]
-id: MOD:01505
-name: iTRAQ4plex-116 reporter+balance reagent O3-acylated threonine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a threonine residue with the Applied Biosystems iTRAQ4plex-116 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "iTRAQ4plex" RELATED PSI-MS-label []
-property_value: DiffAvg "144.10" xsd:float
-property_value: DiffFormula "(12)C 4 (13)C 3 H 12 (14)N 1 (15)N 1 (16)O 1" xsd:string
-property_value: DiffMono "144.102062" xsd:float
-property_value: Formula "(12)C 8 (13)C 3 H 19 (14)N 2 (15)N 1 (16)O 3" xsd:string
-property_value: MassAvg "245.15" xsd:float
-property_value: MassMono "245.149741" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02004
-is_a: MOD:01499
-is_a: MOD:01713
-
-[Term]
-id: MOD:01506
-name: iTRAQ4plex-117, mTRAQ heavy, reporter+balance reagent acylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of a residue with the Applied Biosystems iTRAQ4plex-117 reporter+balance group." [Unimod:214, Unimod:889]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "Applied Biosystems mTRAQ(TM) reagent" RELATED Unimod-alternate []
-synonym: "iTRAQ" RELATED Unimod-interim []
-synonym: "iTRAQ4plex" RELATED PSI-MS-label []
-synonym: "mTRAQ heavy" RELATED Unimod-description []
-synonym: "Representative mass and accurate mass for 116 & 117" RELATED Unimod-description []
-property_value: DiffAvg "144.10" xsd:float
-property_value: DiffFormula "(12)C 4 (13)C 3 H 12 (14)N 1 (15)N 1 (16)O 1" xsd:string
-property_value: DiffMono "144.102062" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:214
-xref: Unimod:889
-is_a: MOD:01428
-is_a: MOD:01429
-is_a: MOD:01517
-is_a: MOD:01518
-is_a: MOD:01863
-
-[Term]
-id: MOD:01507
-name: iTRAQ4plex-117, mTRAQ heavy, reporter+balance reagent acylated N-terminal
-def: "A protein modification that effectively replaces a hydrogen atom of a protein N-terminal with the Applied Biosystems iTRAQ4plex-117 reporter+balance group." [OMSSA:176, OMSSA:211, Unimod:214#N-term, Unimod:889#N-term]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "Applied Biosystems mTRAQ(TM) reagent" RELATED Unimod-alternate []
-synonym: "iTRAQ" RELATED Unimod-interim []
-synonym: "iTRAQ117nterm" EXACT OMSSA-label []
-synonym: "iTRAQ4plex" RELATED PSI-MS-label []
-synonym: "mTRAQ heavy" RELATED Unimod-description []
-synonym: "mTRAQ heavy on nterm" EXACT OMSSA-label []
-synonym: "Representative mass and accurate mass for 116 & 117" RELATED Unimod-description []
-property_value: DiffAvg "144.10" xsd:float
-property_value: DiffFormula "(12)C 4 (13)C 3 H 12 (14)N 1 (15)N 1 (16)O 1" xsd:string
-property_value: DiffMono "144.102062" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:214
-xref: Unimod:889
-is_a: MOD:01506
-is_a: MOD:01711
-
-[Term]
-id: MOD:01508
-name: iTRAQ4plex-117, mTRAQ heavy, reporter+balance reagent N6-acylated lysine
-def: "A protein modification that effectively replaces the N6-hydrogen atom of a lysine residue with the Applied Biosystems iTRAQ4plex-117 reporter+balance group." [OMSSA:177, OMSSA:212, Unimod:214#K, Unimod:889#K]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "Applied Biosystems mTRAQ(TM) reagent" RELATED Unimod-alternate []
-synonym: "iTRAQ" RELATED Unimod-interim []
-synonym: "iTRAQ117K" EXACT OMSSA-label []
-synonym: "iTRAQ4plex" RELATED PSI-MS-label []
-synonym: "mTRAQ heavy" RELATED Unimod-description []
-synonym: "mTRAQ heavy on K" EXACT OMSSA-label []
-synonym: "Representative mass and accurate mass for 116 & 117" RELATED Unimod-description []
-property_value: DiffAvg "144.10" xsd:float
-property_value: DiffFormula "(12)C 4 (13)C 3 H 12 (14)N 1 (15)N 1 (16)O 1" xsd:string
-property_value: DiffMono "144.102062" xsd:float
-property_value: Formula "(12)C 10 (13)C 3 H 24 N 2 (14)N 1 (15)N 1 O 1 (16)O 1" xsd:string
-property_value: MassAvg "272.20" xsd:float
-property_value: MassMono "272.197025" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:214
-is_a: MOD:01506
-is_a: MOD:01709
-is_a: MOD:01875
-
-[Term]
-id: MOD:01509
-name: iTRAQ4plex-117, mTRAQ heavy, reporter+balance reagent O4'-acylated tyrosine
-def: "A protein modification that effectively replaces the O4'-hydrogen atom of a tyrosine residue with the Applied Biosystems iTRAQ4plex-117 reporter+balance group." [OMSSA:178, OMSSA:213, Unimod:214#Y, Unimod:889#Y]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "Applied Biosystems mTRAQ(TM) reagent" RELATED Unimod-alternate []
-synonym: "iTRAQ" RELATED Unimod-interim []
-synonym: "iTRAQ117Y" EXACT OMSSA-label []
-synonym: "iTRAQ4plex" RELATED PSI-MS-label []
-synonym: "mTRAQ heavy" RELATED Unimod-description []
-synonym: "mTRAQ heavy on Y" EXACT OMSSA-label []
-synonym: "Representative mass and accurate mass for 116 & 117" RELATED Unimod-description []
-property_value: DiffAvg "144.10" xsd:float
-property_value: DiffFormula "(12)C 4 (13)C 3 H 12 (14)N 1 (15)N 1 (16)O 1" xsd:string
-property_value: DiffMono "144.102062" xsd:float
-property_value: Formula "(12)C 13 (13)C 3 H 21 N 1 (14)N 1 (15)N 1 O 2 (16)O 1" xsd:string
-property_value: MassAvg "307.17" xsd:float
-property_value: MassMono "307.165391" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:214
-xref: Unimod:889
-is_a: MOD:00919
-is_a: MOD:01506
-is_a: MOD:01713
-
-[Term]
-id: MOD:01510
-name: iTRAQ4plex-117 reporter+balance reagent N'-acylated histidine
-def: "A protein modification that effectively replaces an N'-hydrogen atom of a histidine residue with the Applied Biosystems iTRAQ4plex-117 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "iTRAQ4plex" RELATED PSI-MS-label []
-property_value: DiffAvg "144.10" xsd:float
-property_value: DiffFormula "(12)C 4 (13)C 3 H 12 (14)N 1 (15)N 1 (16)O 1" xsd:string
-property_value: DiffMono "144.102062" xsd:float
-property_value: Formula "(12)C 10 (13)C 3 H 19 (14)N 4 (15)N 1 (16)O 2" xsd:string
-property_value: MassAvg "281.16" xsd:float
-property_value: MassMono "281.160974" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00909
-is_a: MOD:01506
-is_a: MOD:01709
-
-[Term]
-id: MOD:01511
-name: iTRAQ4plex-117 reporter+balance reagent O3-acylated serine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a serine residue with the Applied Biosystems iTRAQ4plex-117 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "iTRAQ4plex" RELATED PSI-MS-label []
-property_value: DiffAvg "144.10" xsd:float
-property_value: DiffFormula "(12)C 4 (13)C 3 H 12 (14)N 1 (15)N 1 (16)O 1" xsd:string
-property_value: DiffMono "144.102062" xsd:float
-property_value: Formula "(12)C 7 (13)C 3 H 17 (14)N 2 (15)N 1 (16)O 3" xsd:string
-property_value: MassAvg "231.13" xsd:float
-property_value: MassMono "231.134091" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02003
-is_a: MOD:01506
-is_a: MOD:01713
-
-[Term]
-id: MOD:01512
-name: iTRAQ4plex-117 reporter+balance reagent O3-acylated threonine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a threonine residue with the Applied Biosystems iTRAQ4plex-117 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "iTRAQ4plex" RELATED PSI-MS-label []
-property_value: DiffAvg "144.10" xsd:float
-property_value: DiffFormula "(12)C 4 (13)C 3 H 12 (14)N 1 (15)N 1 (16)O 1" xsd:string
-property_value: DiffMono "144.102062" xsd:float
-property_value: Formula "(12)C 8 (13)C 3 H 19 (14)N 2 (15)N 1 (16)O 3" xsd:string
-property_value: MassAvg "245.15" xsd:float
-property_value: MassMono "245.149741" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02004
-is_a: MOD:01506
-is_a: MOD:01713
-
-[Term]
-id: MOD:01513
-name: modifications with monoisotopic mass differences that are nominally equal at a resolution below 0.1 Da
-def: "Modifications that have monoisotopic mass differences from their respective origins that are nominally equal (sometimes called isobaric) at a resolution below 0.1 Da." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:00538
-
-[Term]
-id: MOD:01514
-name: modifications with monoisotopic mass differences that are nominally equal at a resolution below 0.01 Da
-def: "Modifications that have monoisotopic mass differences from their respective origins that are nominally equal (sometimes called isobaric) at a resolution below 0.01 Da." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:01513
-
-[Term]
-id: MOD:01515
-name: modifications with monoisotopic mass differences that are nominally equal at a resolution below 0.000001 Da
-def: "Modifications that have monoisotopic mass differences from their respective origins that are nominally equal (sometimes called isobaric) at a resolution below 0.000001 Da." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:01514
-
-[Term]
-id: MOD:01516
-name: modifications with monoisotopic mass diferences that are nominally equal at 144.099-144.106 Da.
-def: "Modifications that have monoisotopic mass differences from their respective origins of 144.099-144.106 Da." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:01514
-
-[Term]
-id: MOD:01517
-name: modifications with monoisotopic mass differences that are nominally equal at 144.102062 Da
-def: "Modifications that have monoisotopic mass differences from their respective origins of 144.102062 Da." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:01515
-is_a: MOD:01516
-
-[Term]
-id: MOD:01518
-name: iTRAQ4plex reporter+balance reagent acylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of a residue with one of the Applied Biosystems iTRAQ4plex reagent reporter+balance groups." [Unimod:214]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:214
-is_a: MOD:01426
-is_a: MOD:01705
-
-[Term]
-id: MOD:01519
-name: reporter fragment
-def: "A distinct molecular entity produced from a protein or a protein modification as the result of a fragmentation process." [PubMed:18688235]
-comment: The reporter fragment is either itself a modification consisting of atoms derived from the original amino acid residues, or its detection can be taken as evidence that particular modified residues had been present.
-subset: PSI-MOD-slim
-is_a: MOD:01156
-
-[Term]
-id: MOD:01520
-name: modification reporter fragment
-def: "A distinct molecular entity produced as the result of a fragmentation process performed on a particular modified residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:01519
-
-[Term]
-id: MOD:01521
-name: iTRAQ4plex reporter fragment
-def: "A protein modification reporter fragment produced by an Applied Biosystems iTRAQ4plex reagent derivatized residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:01520
-
-[Term]
-id: MOD:01522
-name: iTRAQ4plex-114 reporter fragment
-def: "The protein modification reporter fragment produced by an Applied Biosystems iTRAQ4plex 114 reagent derivatized residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "4-methyl-1-methylidenepiperazin-1-ium" EXACT PSI-MOD-alternate []
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "(12)C 5 (13)C 1 H 13 (14)N 2" xsd:string
-property_value: MassAvg "114.11" xsd:float
-property_value: MassMono "114.110680" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01521
-relationship: derives_from MOD:01485
-
-[Term]
-id: MOD:01523
-name: iTRAQ4plex-115 reporter fragment
-def: "The protein modification reporter fragment produced by an Applied Biosystems iTRAQ4plex 115 reagent derivatized residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "4-methyl-1-methylidenepiperazin-1-ium" EXACT PSI-MOD-alternate []
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "(12)C 5 (13)C 1 H 13 (14)N 1 (15)N 1" xsd:string
-property_value: MassAvg "115.11" xsd:float
-property_value: MassMono "115.107715" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01521
-relationship: derives_from MOD:01492
-
-[Term]
-id: MOD:01524
-name: iTRAQ4plex-116 reporter fragment
-def: "The protein modification reporter fragment produced by an Applied Biosystems iTRAQ4plex 116 reagent derivatized residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "4-methyl-1-methylidenepiperazin-1-ium" EXACT PSI-MOD-alternate []
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "(12)C 4 (13)C 2 H 13 (14)N 1 (15)N 1" xsd:string
-property_value: MassAvg "116.11" xsd:float
-property_value: MassMono "116.111069" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01521
-relationship: derives_from MOD:01499
-
-[Term]
-id: MOD:01525
-name: iTRAQ4plex-117, mTRAQ heavy, reporter fragment
-def: "The protein modification reporter fragment produced by an Applied Biosystems iTRAQ4plex 117 reagent derivatized residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "4-methyl-1-methylidenepiperazin-1-ium" EXACT PSI-MOD-alternate []
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "(12)C 3 (13)C 3 H 13 (14)N 1 (15)N 1" xsd:string
-property_value: MassAvg "117.11" xsd:float
-property_value: MassMono "117.114424" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01521
-is_a: MOD:01870
-relationship: derives_from MOD:01506
-
-[Term]
-id: MOD:01526
-name: iTRAQ8plex reporter+balance reagent acylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of a residue with one of the Applied Biosystems iTRAQ8plex reagent reporter+balance groups." [Unimod:730]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:730
-is_a: MOD:01426
-is_a: MOD:01705
-
-[Term]
-id: MOD:01527
-name: residue reporter fragment
-def: "A distinct molecular entity produced from a particular amino acid residue as the result of a fragmentation process." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:01519
-
-[Term]
-id: MOD:01528
-name: iTRAQ8plex-113 reporter+balance reagent acylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of a residue with the Applied Biosystems iTRAQ8plex-113 reporter+balance group." [Unimod:730]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex" RELATED Unimod-interim []
-synonym: "iTRAQ8plex:13C(7)15N(1)" RELATED Unimod-alternate []
-synonym: "Representative mass and accurate mass for 113, 114, 116 & 117" RELATED Unimod-description []
-property_value: DiffAvg "304.21" xsd:float
-property_value: DiffFormula "(12)C 7 (13)C 7 H 24 (14)N 3 (15)N 1 (16)O 3" xsd:string
-property_value: DiffMono "304.205359" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:730
-is_a: MOD:01428
-is_a: MOD:01429
-is_a: MOD:01526
-is_a: MOD:01591
-
-[Term]
-id: MOD:01529
-name: iTRAQ8plex-113 reporter+balance reagent acylated N-terminal
-def: "A protein modification that effectively replaces a hydrogen atom of a protein N-terminal with the Applied Biosystems iTRAQ8plex-113 reporter+balance group." [Unimod:730#N-term]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex" RELATED Unimod-interim []
-synonym: "iTRAQ8plex:13C(7)15N(1)" RELATED Unimod-alternate []
-synonym: "Representative mass and accurate mass for 113, 114, 116 & 117" RELATED Unimod-description []
-property_value: DiffAvg "304.21" xsd:float
-property_value: DiffFormula "(12)C 7 (13)C 7 H 24 (14)N 3 (15)N 1 (16)O 3" xsd:string
-property_value: DiffMono "304.205359" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:730
-is_a: MOD:01528
-is_a: MOD:01712
-
-[Term]
-id: MOD:01530
-name: iTRAQ8plex-113 reporter+balance reagent N6-acylated lysine
-def: "A protein modification that effectively replaces the N6'-hydrogen atom of a lysine residue with the Applied Biosystems iTRAQ8plex-113 reporter+balance group." [Unimod:730#K]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex" RELATED Unimod-interim []
-synonym: "iTRAQ8plex:13C(7)15N(1)" RELATED Unimod-alternate []
-synonym: "Representative mass and accurate mass for 113, 114, 116 & 117" RELATED Unimod-description []
-property_value: DiffAvg "304.21" xsd:float
-property_value: DiffFormula "(12)C 7 (13)C 7 H 24 (14)N 3 (15)N 1 (16)O 3" xsd:string
-property_value: DiffMono "304.205359" xsd:float
-property_value: Formula "(12)C 13 (13)C 7 H 36 (14)N 5 (15)N 1 (16)O 4" xsd:string
-property_value: MassAvg "432.30" xsd:float
-property_value: MassMono "432.300322" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:730
-is_a: MOD:01528
-is_a: MOD:01710
-is_a: MOD:01875
-
-[Term]
-id: MOD:01531
-name: iTRAQ8plex-113 reporter+balance reagent O4'-acylated tyrosine
-def: "A protein modification that effectively replaces the O4'-hydrogen atom of a tyrosine residue with the Applied Biosystems iTRAQ8plex-113 reporter+balance group." [Unimod:730#Y]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex" RELATED Unimod-interim []
-synonym: "iTRAQ8plex:13C(7)15N(1)" RELATED Unimod-alternate []
-synonym: "Representative mass and accurate mass for 113, 114, 116 & 117" RELATED Unimod-description []
-property_value: DiffAvg "304.21" xsd:float
-property_value: DiffFormula "(12)C 7 (13)C 7 H 24 (14)N 3 (15)N 1 (16)O 3" xsd:string
-property_value: DiffMono "304.205359" xsd:float
-property_value: Formula "(12)C 16 (13)C 7 H 33 (14)N 4 (15)N 1 (16)O 5" xsd:string
-property_value: MassAvg "467.27" xsd:float
-property_value: MassMono "467.268688" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:730
-is_a: MOD:00919
-is_a: MOD:01528
-is_a: MOD:01714
-
-[Term]
-id: MOD:01532
-name: iTRAQ8plex-113 reporter+balance reagent N'-acylated histidine
-def: "A protein modification that effectively replaces an N'-hydrogen atom of a histidine residue with the Applied Biosystems iTRAQ8plex-113 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex" RELATED Unimod-interim []
-synonym: "iTRAQ8plex:13C(7)15N(1)" RELATED Unimod-alternate []
-synonym: "Representative mass and accurate mass for 113, 114, 116 & 117" RELATED Unimod-description []
-property_value: DiffAvg "304.21" xsd:float
-property_value: DiffFormula "(12)C 7 (13)C 7 H 24 (14)N 3 (15)N 1 (16)O 3" xsd:string
-property_value: DiffMono "304.205359" xsd:float
-property_value: Formula "(12)C 13 (13)C 7 H 31 (14)N 6 (15)N 1 (16)O 4" xsd:string
-property_value: MassAvg "441.26" xsd:float
-property_value: MassMono "441.264271" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00909
-is_a: MOD:01528
-is_a: MOD:01710
-
-[Term]
-id: MOD:01533
-name: iTRAQ8plex-113 reporter+balance reagent O3-acylated serine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a serine residue with the Applied Biosystems iTRAQ8plex-113 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex" RELATED Unimod-interim []
-synonym: "iTRAQ8plex:13C(7)15N(1)" RELATED Unimod-alternate []
-synonym: "Representative mass and accurate mass for 113, 114, 116 & 117" RELATED Unimod-description []
-property_value: DiffAvg "304.21" xsd:float
-property_value: DiffFormula "(12)C 7 (13)C 7 H 24 (14)N 3 (15)N 1 (16)O 3" xsd:string
-property_value: DiffMono "304.205359" xsd:float
-property_value: Formula "(12)C 10 (13)C 7 H 29 (14)N 4 (15)N 1 (16)O 5" xsd:string
-property_value: MassAvg "391.24" xsd:float
-property_value: MassMono "391.237388" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02003
-is_a: MOD:01528
-is_a: MOD:01714
-
-[Term]
-id: MOD:01534
-name: iTRAQ8plex-113 reporter+balance reagent O3-acylated threonine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a threonine residue with the Applied Biosystems iTRAQ8plex-113 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex" RELATED Unimod-interim []
-synonym: "iTRAQ8plex:13C(7)15N(1)" RELATED Unimod-alternate []
-synonym: "Representative mass and accurate mass for 113, 114, 116 & 117" RELATED Unimod-description []
-property_value: DiffAvg "304.21" xsd:float
-property_value: DiffFormula "(12)C 7 (13)C 7 H 24 (14)N 3 (15)N 1 (16)O 3" xsd:string
-property_value: DiffMono "304.205359" xsd:float
-property_value: Formula "(12)C 11 (13)C 7 H 31 (14)N 4 (15)N 1 (16)O 5" xsd:string
-property_value: MassAvg "405.25" xsd:float
-property_value: MassMono "405.253038" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02004
-is_a: MOD:01528
-is_a: MOD:01714
-
-[Term]
-id: MOD:01535
-name: iTRAQ8plex-114 reporter+balance reagent acylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of a residue with the Applied Biosystems iTRAQ8plex-114 reporter+balance group." [Unimod:730]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex" RELATED Unimod-interim []
-synonym: "iTRAQ8plex:13C(7)15N(1)" RELATED Unimod-alternate []
-synonym: "Representative mass and accurate mass for 113, 114, 116 & 117" RELATED Unimod-description []
-property_value: DiffAvg "304.21" xsd:float
-property_value: DiffFormula "(12)C 7 (13)C 7 H 24 (14)N 3 (15)N 1 (16)O 3" xsd:string
-property_value: DiffMono "304.205359" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:730
-is_a: MOD:01428
-is_a: MOD:01429
-is_a: MOD:01526
-is_a: MOD:01591
-
-[Term]
-id: MOD:01536
-name: iTRAQ8plex-114 reporter+balance reagent acylated N-terminal
-def: "A protein modification that effectively replaces a hydrogen atom of a protein N-terminal with the Applied Biosystems iTRAQ8plex-114 reporter+balance group." [Unimod:730#N-term]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex" RELATED Unimod-interim []
-synonym: "iTRAQ8plex:13C(7)15N(1)" RELATED Unimod-alternate []
-synonym: "Representative mass and accurate mass for 113, 114, 116 & 117" RELATED Unimod-description []
-property_value: DiffAvg "304.21" xsd:float
-property_value: DiffFormula "(12)C 7 (13)C 7 H 24 (14)N 3 (15)N 1 (16)O 3" xsd:string
-property_value: DiffMono "304.205359" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:730
-is_a: MOD:01535
-is_a: MOD:01712
-
-[Term]
-id: MOD:01537
-name: iTRAQ8plex-114 reporter+balance reagent N6-acylated lysine
-def: "A protein modification that effectively replaces the N6'-hydrogen atom of a lysine residue with the Applied Biosystems iTRAQ8plex-114 reporter+balance group." [Unimod:730#K]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex" RELATED Unimod-interim []
-synonym: "iTRAQ8plex:13C(7)15N(1)" RELATED Unimod-alternate []
-synonym: "Representative mass and accurate mass for 113, 114, 116 & 117" RELATED Unimod-description []
-property_value: DiffAvg "304.21" xsd:float
-property_value: DiffFormula "(12)C 7 (13)C 7 H 24 (14)N 3 (15)N 1 (16)O 3" xsd:string
-property_value: DiffMono "304.205359" xsd:float
-property_value: Formula "(12)C 13 (13)C 7 H 36 (14)N 5 (15)N 1 (16)O 4" xsd:string
-property_value: MassAvg "432.30" xsd:float
-property_value: MassMono "432.300322" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:730
-is_a: MOD:01535
-is_a: MOD:01710
-is_a: MOD:01875
-
-[Term]
-id: MOD:01538
-name: iTRAQ8plex-114 reporter+balance reagent O4'-acylated tyrosine
-def: "A protein modification that effectively replaces the O4'-hydrogen atom of a tyrosine residue with the Applied Biosystems iTRAQ8plex-114 reporter+balance group." [Unimod:730#Y]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex" RELATED Unimod-interim []
-synonym: "iTRAQ8plex:13C(7)15N(1)" RELATED Unimod-alternate []
-synonym: "Representative mass and accurate mass for 113, 114, 116 & 117" RELATED Unimod-description []
-property_value: DiffAvg "304.21" xsd:float
-property_value: DiffFormula "(12)C 7 (13)C 7 H 24 (14)N 3 (15)N 1 (16)O 3" xsd:string
-property_value: DiffMono "304.205359" xsd:float
-property_value: Formula "(12)C 16 (13)C 7 H 33 (14)N 4 (15)N 1 (16)O 5" xsd:string
-property_value: MassAvg "467.27" xsd:float
-property_value: MassMono "467.268688" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:730
-is_a: MOD:00919
-is_a: MOD:01535
-is_a: MOD:01714
-
-[Term]
-id: MOD:01539
-name: iTRAQ8plex-114 reporter+balance reagent N'-acylated histidine
-def: "A protein modification that effectively replaces an N'-hydrogen atom of a histidine residue with the Applied Biosystems iTRAQ8plex-114 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex" RELATED Unimod-interim []
-synonym: "iTRAQ8plex:13C(7)15N(1)" RELATED Unimod-alternate []
-synonym: "Representative mass and accurate mass for 113, 114, 116 & 117" RELATED Unimod-description []
-property_value: DiffAvg "304.21" xsd:float
-property_value: DiffFormula "(12)C 7 (13)C 7 H 24 (14)N 3 (15)N 1 (16)O 3" xsd:string
-property_value: DiffMono "304.205359" xsd:float
-property_value: Formula "(12)C 13 (13)C 7 H 31 (14)N 6 (15)N 1 (16)O 4" xsd:string
-property_value: MassAvg "441.26" xsd:float
-property_value: MassMono "441.264271" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00909
-is_a: MOD:01535
-is_a: MOD:01710
-
-[Term]
-id: MOD:01540
-name: iTRAQ8plex-114 reporter+balance reagent O3-acylated serine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a serine residue with the Applied Biosystems iTRAQ8plex-114 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "304.21" xsd:float
-property_value: DiffFormula "(12)C 7 (13)C 7 H 24 (14)N 3 (15)N 1 (16)O 3" xsd:string
-property_value: DiffMono "304.205359" xsd:float
-property_value: Formula "(12)C 10 (13)C 7 H 29 (14)N 4 (15)N 1 (16)O 5" xsd:string
-property_value: MassAvg "391.24" xsd:float
-property_value: MassMono "391.237388" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02003
-is_a: MOD:01535
-is_a: MOD:01714
-
-[Term]
-id: MOD:01541
-name: iTRAQ8plex-114 reporter+balance reagent O3-acylated threonine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a threonine residue with the Applied Biosystems iTRAQ8plex-114 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "304.21" xsd:float
-property_value: DiffFormula "(12)C 7 (13)C 7 H 24 (14)N 3 (15)N 1 (16)O 3" xsd:string
-property_value: DiffMono "304.205359" xsd:float
-property_value: Formula "(12)C 11 (13)C 7 H 31 (14)N 4 (15)N 1 (16)O 5" xsd:string
-property_value: MassAvg "405.25" xsd:float
-property_value: MassMono "405.253038" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02004
-is_a: MOD:01535
-is_a: MOD:01714
-
-[Term]
-id: MOD:01542
-name: iTRAQ8plex-115 reporter+balance reagent acylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of a residue with the Applied Biosystems iTRAQ8plex-115 reporter+balance group." [Unimod:731]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Accurate mass for 115, 118, 119 & 121" RELATED Unimod-description []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex:13C(6)15N(2)" RELATED Unimod-interim []
-property_value: DiffAvg "304.20" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 6 H 24 (14)N 2 (15)N 2 (16)O 3" xsd:string
-property_value: DiffMono "304.199039" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:731
-is_a: MOD:01428
-is_a: MOD:01429
-is_a: MOD:01526
-is_a: MOD:01584
-
-[Term]
-id: MOD:01543
-name: iTRAQ8plex-115 reporter+balance reagent acylated N-terminal
-def: "A protein modification that effectively replaces a hydrogen atom of a protein N-terminal with the Applied Biosystems iTRAQ8plex-115 reporter+balance group." [Unimod:731#N-term]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Accurate mass for 115, 118, 119 & 121" RELATED Unimod-description []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex:13C(6)15N(2)" RELATED Unimod-interim []
-property_value: DiffAvg "304.20" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 6 H 24 (14)N 2 (15)N 2 (16)O 3" xsd:string
-property_value: DiffMono "304.199039" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:731
-is_a: MOD:01542
-is_a: MOD:01712
-
-[Term]
-id: MOD:01544
-name: iTRAQ8plex-115 reporter+balance reagent N6-acylated lysine
-def: "A protein modification that effectively replaces the N6'-hydrogen atom of a lysine residue with the Applied Biosystems iTRAQ8plex-115 reporter+balance group." [Unimod:731#K]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Accurate mass for 115, 118, 119 & 121" RELATED Unimod-description []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex:13C(6)15N(2)" RELATED Unimod-interim []
-property_value: DiffAvg "304.20" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 6 H 24 (14)N 2 (15)N 2 (16)O 3" xsd:string
-property_value: DiffMono "304.199039" xsd:float
-property_value: Formula "(12)C 14 (13)C 6 H 36 (14)N 4 (15)N 2 (16)O 4" xsd:string
-property_value: MassAvg "432.29" xsd:float
-property_value: MassMono "432.294002" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:731
-is_a: MOD:01542
-is_a: MOD:01710
-is_a: MOD:01875
-
-[Term]
-id: MOD:01545
-name: iTRAQ8plex-115 reporter+balance reagent O4'-acylated tyrosine
-def: "A protein modification that effectively replaces the O4'-hydrogen atom of a tyrosine residue with the Applied Biosystems iTRAQ8plex-115 reporter+balance group." [Unimod:731#Y]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Accurate mass for 115, 118, 119 & 121" RELATED Unimod-description []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex:13C(6)15N(2)" RELATED Unimod-interim []
-property_value: DiffAvg "304.20" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 6 H 24 (14)N 2 (15)N 2 (16)O 3" xsd:string
-property_value: DiffMono "304.199039" xsd:float
-property_value: Formula "(12)C 17 (13)C 6 H 33 (14)N 3 (15)N 2 (16)O 5" xsd:string
-property_value: MassAvg "467.26" xsd:float
-property_value: MassMono "467.262368" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:731
-is_a: MOD:00919
-is_a: MOD:01542
-is_a: MOD:01714
-
-[Term]
-id: MOD:01546
-name: iTRAQ8plex-115 reporter+balance reagent N'-derivatized histidine
-def: "A protein modification that effectively replaces an N'-hydrogen atom of a histidine residue with the Applied Biosystems iTRAQ8plex-115 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "304.20" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 6 H 24 (14)N 2 (15)N 2 (16)O 3" xsd:string
-property_value: DiffMono "304.199039" xsd:float
-property_value: Formula "(12)C 14 (13)C 6 H 31 (14)N 5 (15)N 2 (16)O 4" xsd:string
-property_value: MassAvg "441.26" xsd:float
-property_value: MassMono "441.257951" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00909
-is_a: MOD:01542
-is_a: MOD:01710
-
-[Term]
-id: MOD:01547
-name: iTRAQ8plex-115 reporter+balance reagent O3-acylated serine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a serine residue with the Applied Biosystems iTRAQ8plex-115 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "304.20" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 6 H 24 (14)N 2 (15)N 2 (16)O 3" xsd:string
-property_value: DiffMono "304.199039" xsd:float
-property_value: Formula "(12)C 11 (13)C 6 H 29 (14)N 3 (15)N 2 (16)O 5" xsd:string
-property_value: MassAvg "391.23" xsd:float
-property_value: MassMono "391.231068" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02003
-is_a: MOD:01542
-is_a: MOD:01714
-
-[Term]
-id: MOD:01548
-name: iTRAQ8plex-115 reporter+balance reagent O3-acylated threonine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a threonine residue with the Applied Biosystems iTRAQ8plex-115 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "304.20" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 6 H 24 (14)N 2 (15)N 2 (16)O 3" xsd:string
-property_value: DiffMono "304.199039" xsd:float
-property_value: Formula "(12)C 12 (13)C 6 H 31 (14)N 3 (15)N 2 (16)O 5" xsd:string
-property_value: MassAvg "405.25" xsd:float
-property_value: MassMono "405.246718" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02004
-is_a: MOD:01542
-is_a: MOD:01714
-
-[Term]
-id: MOD:01549
-name: iTRAQ8plex-116 reporter+balance reagent acylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of a residue with the Applied Biosystems iTRAQ8plex-116 reporter+balance group." [Unimod:730]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex" RELATED Unimod-interim []
-synonym: "iTRAQ8plex:13C(7)15N(1)" RELATED Unimod-alternate []
-synonym: "Representative mass and accurate mass for 113, 114, 116 & 117" RELATED Unimod-description []
-property_value: DiffAvg "304.21" xsd:float
-property_value: DiffFormula "(12)C 7 (13)C 7 H 24 (14)N 3 (15)N 1 (16)O 3" xsd:string
-property_value: DiffMono "304.205359" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:730
-is_a: MOD:01428
-is_a: MOD:01429
-is_a: MOD:01526
-is_a: MOD:01591
-
-[Term]
-id: MOD:01550
-name: iTRAQ8plex-116 reporter+balance reagent acylated N-terminal
-def: "A protein modification that effectively replaces a hydrogen atom of a protein N-terminal with the Applied Biosystems iTRAQ8plex-116 reporter+balance group." [Unimod:730#N-term]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex" RELATED Unimod-interim []
-synonym: "iTRAQ8plex:13C(7)15N(1)" RELATED Unimod-alternate []
-synonym: "Representative mass and accurate mass for 113, 114, 116 & 117" RELATED Unimod-description []
-property_value: DiffAvg "304.21" xsd:float
-property_value: DiffFormula "(12)C 7 (13)C 7 H 24 (14)N 3 (15)N 1 (16)O 3" xsd:string
-property_value: DiffMono "304.205359" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:730
-is_a: MOD:01549
-is_a: MOD:01712
-
-[Term]
-id: MOD:01551
-name: iTRAQ8plex-116 reporter+balance reagent N6-acylated lysine
-def: "A protein modification that effectively replaces the N6'-hydrogen atom of a lysine residue with the Applied Biosystems iTRAQ8plex-116 reporter+balance group." [Unimod:730#K]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex" RELATED Unimod-interim []
-synonym: "iTRAQ8plex:13C(7)15N(1)" RELATED Unimod-alternate []
-synonym: "Representative mass and accurate mass for 113, 114, 116 & 117" RELATED Unimod-description []
-property_value: DiffAvg "304.21" xsd:float
-property_value: DiffFormula "(12)C 7 (13)C 7 H 24 (14)N 3 (15)N 1 (16)O 3" xsd:string
-property_value: DiffMono "304.205359" xsd:float
-property_value: Formula "(12)C 13 (13)C 7 H 36 (14)N 5 (15)N 1 (16)O 4" xsd:string
-property_value: MassAvg "432.30" xsd:float
-property_value: MassMono "432.300322" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:730
-is_a: MOD:01549
-is_a: MOD:01710
-is_a: MOD:01875
-
-[Term]
-id: MOD:01552
-name: iTRAQ8plex-116 reporter+balance reagent O4'-acylated tyrosine
-def: "A protein modification that effectively replaces the O4'-hydrogen atom of a tyrosine residue with the Applied Biosystems iTRAQ8plex-116 reporter+balance group." [Unimod:730#Y]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex" RELATED Unimod-interim []
-synonym: "iTRAQ8plex:13C(7)15N(1)" RELATED Unimod-alternate []
-synonym: "Representative mass and accurate mass for 113, 114, 116 & 117" RELATED Unimod-description []
-property_value: DiffAvg "304.21" xsd:float
-property_value: DiffFormula "(12)C 7 (13)C 7 H 24 (14)N 3 (15)N 1 (16)O 3" xsd:string
-property_value: DiffMono "304.205359" xsd:float
-property_value: Formula "(12)C 16 (13)C 7 H 33 (14)N 4 (15)N 1 (16)O 5" xsd:string
-property_value: MassAvg "467.27" xsd:float
-property_value: MassMono "467.268688" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:730
-is_a: MOD:00919
-is_a: MOD:01549
-is_a: MOD:01714
-
-[Term]
-id: MOD:01553
-name: iTRAQ8plex-116 reporter+balance reagent N'-acylated histidine
-def: "A protein modification that effectively replaces an N'-hydrogen atom of a histidine residue with the Applied Biosystems iTRAQ8plex-116 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "304.21" xsd:float
-property_value: DiffFormula "(12)C 7 (13)C 7 H 24 (14)N 3 (15)N 1 (16)O 3" xsd:string
-property_value: DiffMono "304.205359" xsd:float
-property_value: Formula "(12)C 13 (13)C 7 H 31 (14)N 6 (15)N 1 (16)O 4" xsd:string
-property_value: MassAvg "441.26" xsd:float
-property_value: MassMono "441.264271" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00909
-is_a: MOD:01549
-is_a: MOD:01710
-
-[Term]
-id: MOD:01554
-name: iTRAQ8plex-116 reporter+balance reagent O3-acylated serine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a serine residue with the Applied Biosystems iTRAQ8plex-116 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "304.21" xsd:float
-property_value: DiffFormula "(12)C 7 (13)C 7 H 24 (14)N 3 (15)N 1 (16)O 3" xsd:string
-property_value: DiffMono "304.205359" xsd:float
-property_value: Formula "(12)C 10 (13)C 7 H 29 (14)N 4 (15)N 1 (16)O 5" xsd:string
-property_value: MassAvg "391.24" xsd:float
-property_value: MassMono "391.237388" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02003
-is_a: MOD:01549
-is_a: MOD:01714
-
-[Term]
-id: MOD:01555
-name: iTRAQ8plex-116 reporter+balance reagent O3-acylated threonine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a threonine residue with the Applied Biosystems iTRAQ8plex-116 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "304.21" xsd:float
-property_value: DiffFormula "(12)C 7 (13)C 7 H 24 (14)N 3 (15)N 1 (16)O 3" xsd:string
-property_value: DiffMono "304.205359" xsd:float
-property_value: Formula "(12)C 11 (13)C 7 H 31 (14)N 4 (15)N 1 (16)O 5" xsd:string
-property_value: MassAvg "405.25" xsd:float
-property_value: MassMono "405.253038" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02004
-is_a: MOD:01549
-is_a: MOD:01714
-
-[Term]
-id: MOD:01556
-name: iTRAQ8plex-117 reporter+balance reagent acylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of a residue with the Applied Biosystems iTRAQ8plex-117 reporter+balance group." [Unimod:730]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex" RELATED Unimod-interim []
-synonym: "iTRAQ8plex:13C(7)15N(1)" RELATED Unimod-alternate []
-synonym: "Representative mass and accurate mass for 113, 114, 116 & 117" RELATED Unimod-description []
-property_value: DiffAvg "304.21" xsd:float
-property_value: DiffFormula "(12)C 7 (13)C 7 H 24 (14)N 3 (15)N 1 (16)O 3" xsd:string
-property_value: DiffMono "304.205359" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:730
-is_a: MOD:01428
-is_a: MOD:01429
-is_a: MOD:01526
-is_a: MOD:01591
-
-[Term]
-id: MOD:01557
-name: iTRAQ8plex-117 reporter+balance reagent acylated N-terminal
-def: "A protein modification that effectively replaces a hydrogen atom of a protein N-terminal with the Applied Biosystems iTRAQ8plex-117 reporter+balance group." [Unimod:730#N-term]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex" RELATED Unimod-interim []
-synonym: "iTRAQ8plex:13C(7)15N(1)" RELATED Unimod-alternate []
-synonym: "Representative mass and accurate mass for 113, 114, 116 & 117" RELATED Unimod-description []
-property_value: DiffAvg "304.21" xsd:float
-property_value: DiffFormula "(12)C 7 (13)C 7 H 24 (14)N 3 (15)N 1 (16)O 3" xsd:string
-property_value: DiffMono "304.205359" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:730
-is_a: MOD:01556
-is_a: MOD:01712
-
-[Term]
-id: MOD:01558
-name: iTRAQ8plex-117 reporter+balance reagent N6-acylated lysine
-def: "A protein modification that effectively replaces the N6'-hydrogen atom of a lysine residue with the Applied Biosystems iTRAQ8plex-117 reporter+balance group." [Unimod:730#K]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex" RELATED Unimod-interim []
-synonym: "iTRAQ8plex:13C(7)15N(1)" RELATED Unimod-alternate []
-synonym: "Representative mass and accurate mass for 113, 114, 116 & 117" RELATED Unimod-description []
-property_value: DiffAvg "304.21" xsd:float
-property_value: DiffFormula "(12)C 7 (13)C 7 H 24 (14)N 3 (15)N 1 (16)O 3" xsd:string
-property_value: DiffMono "304.205359" xsd:float
-property_value: Formula "(12)C 13 (13)C 7 H 36 (14)N 5 (15)N 1 (16)O 4" xsd:string
-property_value: MassAvg "432.30" xsd:float
-property_value: MassMono "432.300322" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:730
-is_a: MOD:01556
-is_a: MOD:01710
-is_a: MOD:01875
-
-[Term]
-id: MOD:01559
-name: iTRAQ8plex-117 reporter+balance reagent O4'-acylated tyrosine
-def: "A protein modification that effectively replaces the O4'-hydrogen atom of a tyrosine residue with the Applied Biosystems iTRAQ8plex-117 reporter+balance group." [Unimod:730#Y]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex" RELATED Unimod-interim []
-synonym: "iTRAQ8plex:13C(7)15N(1)" RELATED Unimod-alternate []
-synonym: "Representative mass and accurate mass for 113, 114, 116 & 117" RELATED Unimod-description []
-property_value: DiffAvg "304.21" xsd:float
-property_value: DiffFormula "(12)C 7 (13)C 7 H 24 (14)N 3 (15)N 1 (16)O 3" xsd:string
-property_value: DiffMono "304.205359" xsd:float
-property_value: Formula "(12)C 16 (13)C 7 H 33 (14)N 4 (15)N 1 (16)O 5" xsd:string
-property_value: MassAvg "467.27" xsd:float
-property_value: MassMono "467.268688" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:730
-is_a: MOD:00919
-is_a: MOD:01556
-is_a: MOD:01714
-
-[Term]
-id: MOD:01560
-name: iTRAQ8plex-117 reporter+balance reagent N'-acylated histidine
-def: "A protein modification that effectively replaces an N'-hydrogen atom of a histidine residue with the Applied Biosystems iTRAQ8plex-117 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "304.21" xsd:float
-property_value: DiffFormula "(12)C 7 (13)C 7 H 24 (14)N 3 (15)N 1 (16)O 3" xsd:string
-property_value: DiffMono "304.205359" xsd:float
-property_value: Formula "(12)C 13 (13)C 7 H 31 (14)N 6 (15)N 1 (16)O 4" xsd:string
-property_value: MassAvg "441.26" xsd:float
-property_value: MassMono "441.264271" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00909
-is_a: MOD:01556
-is_a: MOD:01710
-
-[Term]
-id: MOD:01561
-name: iTRAQ8plex-117 reporter+balance reagent O3-acylated serine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a serine residue with the Applied Biosystems iTRAQ8plex-117 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "304.21" xsd:float
-property_value: DiffFormula "(12)C 7 (13)C 7 H 24 (14)N 3 (15)N 1 (16)O 3" xsd:string
-property_value: DiffMono "304.205359" xsd:float
-property_value: Formula "(12)C 10 (13)C 7 H 29 (14)N 4 (15)N 1 (16)O 5" xsd:string
-property_value: MassAvg "391.24" xsd:float
-property_value: MassMono "391.237388" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02003
-is_a: MOD:01556
-is_a: MOD:01714
-
-[Term]
-id: MOD:01562
-name: iTRAQ8plex-117 reporter+balance reagent O3-acylated threonine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a threonine residue with the Applied Biosystems iTRAQ8plex-117 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "304.21" xsd:float
-property_value: DiffFormula "(12)C 7 (13)C 7 H 24 (14)N 3 (15)N 1 (16)O 3" xsd:string
-property_value: DiffMono "304.205359" xsd:float
-property_value: Formula "(12)C 11 (13)C 7 H 31 (14)N 4 (15)N 1 (16)O 5" xsd:string
-property_value: MassAvg "405.25" xsd:float
-property_value: MassMono "405.253038" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02004
-is_a: MOD:01556
-is_a: MOD:01714
-
-[Term]
-id: MOD:01563
-name: iTRAQ8plex-118 reporter+balance reagent acylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of a residue with the Applied Biosystems iTRAQ8plex-118 reporter+balance group." [Unimod:731]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Accurate mass for 115, 118, 119 & 121" RELATED Unimod-description []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex:13C(6)15N(2)" RELATED Unimod-interim []
-property_value: DiffAvg "304.20" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 6 H 24 (14)N 2 (15)N 2 (16)O 3" xsd:string
-property_value: DiffMono "304.199039" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:731
-is_a: MOD:01428
-is_a: MOD:01429
-is_a: MOD:01526
-is_a: MOD:01584
-
-[Term]
-id: MOD:01564
-name: iTRAQ8plex-118 reporter+balance reagent acylated N-terminal
-def: "A protein modification that effectively replaces a hydrogen atom of a protein N-terminal with the Applied Biosystems iTRAQ8plex-118 reporter+balance group." [Unimod:731#N-term]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Accurate mass for 115, 118, 119 & 121" RELATED Unimod-description []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex:13C(6)15N(2)" RELATED Unimod-interim []
-property_value: DiffAvg "304.20" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 6 H 24 (14)N 2 (15)N 2 (16)O 3" xsd:string
-property_value: DiffMono "304.199039" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:731
-is_a: MOD:01563
-is_a: MOD:01712
-
-[Term]
-id: MOD:01565
-name: iTRAQ8plex-118 reporter+balance reagent N6-acylated lysine
-def: "A protein modification that effectively replaces the N6'-hydrogen atom of a lysine residue with the Applied Biosystems iTRAQ8plex-118 reporter+balance group." [Unimod:731#K]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Accurate mass for 115, 118, 119 & 121" RELATED Unimod-description []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex:13C(6)15N(2)" RELATED Unimod-interim []
-property_value: DiffAvg "304.20" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 6 H 24 (14)N 2 (15)N 2 (16)O 3" xsd:string
-property_value: DiffMono "304.199039" xsd:float
-property_value: Formula "(12)C 14 (13)C 6 H 36 (14)N 4 (15)N 2 (16)O 4" xsd:string
-property_value: MassAvg "432.29" xsd:float
-property_value: MassMono "432.294002" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:731
-is_a: MOD:01563
-is_a: MOD:01710
-is_a: MOD:01875
-
-[Term]
-id: MOD:01566
-name: iTRAQ8plex-118 reporter+balance reagent O4'-acylated tyrosine
-def: "A protein modification that effectively replaces the O4'-hydrogen atom of a tyrosine residue with the Applied Biosystems iTRAQ8plex-118 reporter+balance group." [Unimod:731#Y]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Accurate mass for 115, 118, 119 & 121" RELATED Unimod-description []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex:13C(6)15N(2)" RELATED Unimod-interim []
-property_value: DiffAvg "304.20" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 6 H 24 (14)N 2 (15)N 2 (16)O 3" xsd:string
-property_value: DiffMono "304.199039" xsd:float
-property_value: Formula "(12)C 17 (13)C 6 H 33 (14)N 3 (15)N 2 (16)O 5" xsd:string
-property_value: MassAvg "467.26" xsd:float
-property_value: MassMono "467.262368" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:731
-is_a: MOD:00919
-is_a: MOD:01563
-is_a: MOD:01714
-
-[Term]
-id: MOD:01567
-name: iTRAQ8plex-118 reporter+balance reagent N'-acylated histidine
-def: "A protein modification that effectively replaces an N'-hydrogen atom of a histidine residue with the Applied Biosystems iTRAQ8plex-118 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "304.20" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 6 H 24 (14)N 2 (15)N 2 (16)O 3" xsd:string
-property_value: DiffMono "304.199039" xsd:float
-property_value: Formula "(12)C 14 (13)C 6 H 31 (14)N 5 (15)N 2 (16)O 4" xsd:string
-property_value: MassAvg "441.26" xsd:float
-property_value: MassMono "441.257951" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00909
-is_a: MOD:01563
-is_a: MOD:01710
-
-[Term]
-id: MOD:01568
-name: iTRAQ8plex-118 reporter+balance reagent O3-acylated serine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a serine residue with the Applied Biosystems iTRAQ8plex-118 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "304.20" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 6 H 24 (14)N 2 (15)N 2 (16)O 3" xsd:string
-property_value: DiffMono "304.199039" xsd:float
-property_value: Formula "(12)C 11 (13)C 6 H 29 (14)N 3 (15)N 2 (16)O 5" xsd:string
-property_value: MassAvg "391.23" xsd:float
-property_value: MassMono "391.231068" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02003
-is_a: MOD:01563
-is_a: MOD:01714
-
-[Term]
-id: MOD:01569
-name: iTRAQ8plex-118 reporter+balance reagent O3-acylated threonine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a threonine residue with the Applied Biosystems iTRAQ8plex-118 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "304.20" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 6 H 24 (14)N 2 (15)N 2 (16)O 3" xsd:string
-property_value: DiffMono "304.199039" xsd:float
-property_value: Formula "(12)C 12 (13)C 6 H 31 (14)N 3 (15)N 2 (16)O 5" xsd:string
-property_value: MassAvg "405.25" xsd:float
-property_value: MassMono "405.246718" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02004
-is_a: MOD:01563
-is_a: MOD:01714
-
-[Term]
-id: MOD:01570
-name: iTRAQ8plex-119 reporter+balance reagent acylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of a residue with the Applied Biosystems iTRAQ8plex-119 reporter+balance group." [Unimod:731]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Accurate mass for 115, 118, 119 & 121" RELATED Unimod-description []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex:13C(6)15N(2)" RELATED Unimod-interim []
-property_value: DiffAvg "304.20" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 6 H 24 (14)N 2 (15)N 2 (16)O 3" xsd:string
-property_value: DiffMono "304.199039" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:731
-is_a: MOD:01428
-is_a: MOD:01429
-is_a: MOD:01526
-is_a: MOD:01584
-
-[Term]
-id: MOD:01571
-name: iTRAQ8plex-119 reporter+balance reagent acylated N-terminal
-def: "A protein modification that effectively replaces a hydrogen atom of a protein N-terminal with the Applied Biosystems iTRAQ8plex-119 reporter+balance group." [Unimod:731#N-term]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Accurate mass for 115, 118, 119 & 121" RELATED Unimod-description []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex:13C(6)15N(2)" RELATED Unimod-interim []
-property_value: DiffAvg "304.20" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 6 H 24 (14)N 2 (15)N 2 (16)O 3" xsd:string
-property_value: DiffMono "304.199039" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:731
-is_a: MOD:01570
-is_a: MOD:01712
-
-[Term]
-id: MOD:01572
-name: iTRAQ8plex-119 reporter+balance reagent N6-acylated lysine
-def: "A protein modification that effectively replaces the N6'-hydrogen atom of a lysine residue with the Applied Biosystems iTRAQ8plex-119 reporter+balance group." [Unimod:731#K]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Accurate mass for 115, 118, 119 & 121" RELATED Unimod-description []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex:13C(6)15N(2)" RELATED Unimod-interim []
-property_value: DiffAvg "304.20" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 6 H 24 (14)N 2 (15)N 2 (16)O 3" xsd:string
-property_value: DiffMono "304.199039" xsd:float
-property_value: Formula "(12)C 14 (13)C 6 H 36 (14)N 4 (15)N 2 (16)O 4" xsd:string
-property_value: MassAvg "432.29" xsd:float
-property_value: MassMono "432.294002" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:731
-is_a: MOD:01570
-is_a: MOD:01710
-is_a: MOD:01875
-
-[Term]
-id: MOD:01573
-name: iTRAQ8plex-119 reporter+balance reagent O4'-acylated tyrosine
-def: "A protein modification that effectively replaces the O4'-hydrogen atom of a tyrosine residue with the Applied Biosystems iTRAQ8plex-119 reporter+balance group." [Unimod:731#Y]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Accurate mass for 115, 118, 119 & 121" RELATED Unimod-description []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex:13C(6)15N(2)" RELATED Unimod-interim []
-property_value: DiffAvg "304.20" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 6 H 24 (14)N 2 (15)N 2 (16)O 3" xsd:string
-property_value: DiffMono "304.199039" xsd:float
-property_value: Formula "(12)C 17 (13)C 6 H 33 (14)N 3 (15)N 2 (16)O 5" xsd:string
-property_value: MassAvg "467.26" xsd:float
-property_value: MassMono "467.262368" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:731
-is_a: MOD:00919
-is_a: MOD:01570
-is_a: MOD:01714
-
-[Term]
-id: MOD:01574
-name: iTRAQ8plex-119 reporter+balance reagent N'-acylated histidine
-def: "A protein modification that effectively replaces an N'-hydrogen atom of a histidine residue with the Applied Biosystems iTRAQ8plex-119 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "304.20" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 6 H 24 (14)N 2 (15)N 2 (16)O 3" xsd:string
-property_value: DiffMono "304.199039" xsd:float
-property_value: Formula "(12)C 14 (13)C 6 H 31 (14)N 5 (15)N 2 (16)O 4" xsd:string
-property_value: MassAvg "441.26" xsd:float
-property_value: MassMono "441.257951" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00909
-is_a: MOD:01570
-is_a: MOD:01710
-
-[Term]
-id: MOD:01575
-name: iTRAQ8plex-119 reporter+balance reagent O3-acylated serine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a serine residue with the Applied Biosystems iTRAQ8plex-119 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "304.20" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 6 H 24 (14)N 2 (15)N 2 (16)O 3" xsd:string
-property_value: DiffMono "304.199039" xsd:float
-property_value: Formula "(12)C 11 (13)C 6 H 29 (14)N 3 (15)N 2 (16)O 5" xsd:string
-property_value: MassAvg "391.23" xsd:float
-property_value: MassMono "391.231068" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02003
-is_a: MOD:01570
-is_a: MOD:01714
-
-[Term]
-id: MOD:01576
-name: iTRAQ8plex-119 reporter+balance reagent O3-acylated threonine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a threonine residue with the Applied Biosystems iTRAQ8plex-119 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "304.20" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 6 H 24 (14)N 2 (15)N 2 (16)O 3" xsd:string
-property_value: DiffMono "304.199039" xsd:float
-property_value: Formula "(12)C 12 (13)C 6 H 31 (14)N 3 (15)N 2 (16)O 5" xsd:string
-property_value: MassAvg "405.25" xsd:float
-property_value: MassMono "405.246718" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02004
-is_a: MOD:01570
-is_a: MOD:01714
-
-[Term]
-id: MOD:01577
-name: iTRAQ8plex-121 reporter+balance reagent acylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of a residue with the Applied Biosystems iTRAQ8plex-121 reporter+balance group." [Unimod:731]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Accurate mass for 115, 118, 119 & 121" RELATED Unimod-description []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex:13C(6)15N(2)" RELATED Unimod-interim []
-property_value: DiffAvg "304.20" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 6 H 24 (14)N 2 (15)N 2 (16)O 3" xsd:string
-property_value: DiffMono "304.199039" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:731
-is_a: MOD:01428
-is_a: MOD:01429
-is_a: MOD:01526
-is_a: MOD:01584
-
-[Term]
-id: MOD:01578
-name: iTRAQ8plex-121 reporter+balance reagent acylated N-terminal
-def: "A protein modification that effectively replaces a hydrogen atom of a protein N-terminal with the Applied Biosystems iTRAQ8plex-121 reporter+balance group." [Unimod:731#N-term]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Accurate mass for 115, 118, 119 & 121" RELATED Unimod-description []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex:13C(6)15N(2)" RELATED Unimod-interim []
-property_value: DiffAvg "304.20" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 6 H 24 (14)N 2 (15)N 2 (16)O 3" xsd:string
-property_value: DiffMono "304.199039" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:731
-is_a: MOD:01577
-is_a: MOD:01712
-
-[Term]
-id: MOD:01579
-name: iTRAQ8plex-121 reporter+balance reagent N6-acylated lysine
-def: "A protein modification that effectively replaces the N6'-hydrogen atom of a lysine residue with the Applied Biosystems iTRAQ8plex-121 reporter+balance group." [Unimod:731#K]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Accurate mass for 115, 118, 119 & 121" RELATED Unimod-description []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex:13C(6)15N(2)" RELATED Unimod-interim []
-property_value: DiffAvg "304.20" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 6 H 24 (14)N 2 (15)N 2 (16)O 3" xsd:string
-property_value: DiffMono "304.199039" xsd:float
-property_value: Formula "(12)C 14 (13)C 6 H 36 (14)N 4 (15)N 2 (16)O 4" xsd:string
-property_value: MassAvg "432.29" xsd:float
-property_value: MassMono "432.294002" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:731
-is_a: MOD:01577
-is_a: MOD:01710
-is_a: MOD:01875
-
-[Term]
-id: MOD:01580
-name: iTRAQ8plex-121 reporter+balance reagent O4'-acylated tyrosine
-def: "A protein modification that effectively replaces the O4'-hydrogen atom of a tyrosine residue with the Applied Biosystems iTRAQ8plex-121 reporter+balance group." [Unimod:731#Y]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Accurate mass for 115, 118, 119 & 121" RELATED Unimod-description []
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED Unimod-alternate []
-synonym: "iTRAQ8plex:13C(6)15N(2)" RELATED Unimod-interim []
-property_value: DiffAvg "304.20" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 6 H 24 (14)N 2 (15)N 2 (16)O 3" xsd:string
-property_value: DiffMono "304.199039" xsd:float
-property_value: Formula "(12)C 17 (13)C 6 H 33 (14)N 3 (15)N 2 (16)O 5" xsd:string
-property_value: MassAvg "467.26" xsd:float
-property_value: MassMono "467.262368" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:731
-is_a: MOD:00919
-is_a: MOD:01577
-is_a: MOD:01714
-
-[Term]
-id: MOD:01581
-name: iTRAQ8plex-121 reporter+balance reagent N'-acylated histidine
-def: "A protein modification that effectively replaces an N'-hydrogen atom of a histidine residue with the Applied Biosystems iTRAQ8plex-121 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "304.20" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 6 H 24 (14)N 2 (15)N 2 (16)O 3" xsd:string
-property_value: DiffMono "304.199039" xsd:float
-property_value: Formula "(12)C 14 (13)C 6 H 31 (14)N 5 (15)N 2 (16)O 4" xsd:string
-property_value: MassAvg "441.26" xsd:float
-property_value: MassMono "441.257951" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00909
-is_a: MOD:01577
-is_a: MOD:01710
-
-[Term]
-id: MOD:01582
-name: iTRAQ8plex-121 reporter+balance reagent O3-acylated serine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a serine residue with the Applied Biosystems iTRAQ8plex-121 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "304.20" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 6 H 24 (14)N 2 (15)N 2 (16)O 3" xsd:string
-property_value: DiffMono "304.199039" xsd:float
-property_value: Formula "(12)C 11 (13)C 6 H 29 (14)N 3 (15)N 2 (16)O 5" xsd:string
-property_value: MassAvg "391.23" xsd:float
-property_value: MassMono "391.231068" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02003
-is_a: MOD:01577
-is_a: MOD:01714
-
-[Term]
-id: MOD:01583
-name: iTRAQ8plex-121 reporter+balance reagent O3-acylated threonine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a threonine residue with the Applied Biosystems iTRAQ8plex-121 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "304.20" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 6 H 24 (14)N 2 (15)N 2 (16)O 3" xsd:string
-property_value: DiffMono "304.199039" xsd:float
-property_value: Formula "(12)C 12 (13)C 6 H 31 (14)N 3 (15)N 2 (16)O 5" xsd:string
-property_value: MassAvg "405.25" xsd:float
-property_value: MassMono "405.246718" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02004
-is_a: MOD:01577
-is_a: MOD:01714
-
-[Term]
-id: MOD:01584
-name: modifications with monoisotopic mass differences that are nominally equal at 304.199039 Da
-def: "Modifications that have monoisotopic mass differences from their respective origins of 304.199039 Da." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:01515
-is_a: MOD:01592
-
-[Term]
-id: MOD:01585
-name: O-glycyl-L-serine
-def: "A protein modification that effectively crosslinks an L-serine residue and a glycine residue by an ester bond to form O-glycyl-L-serine." [PubMed:17502423, RESID:AA0495]
-comment: Cross-link 2.
-synonym: "(2S)-2-amino-3-[(aminoacetyl)oxy]propanoic acid" EXACT RESID-systematic []
-synonym: "O-(glycyl)-L-serine" EXACT RESID-name []
-synonym: "O3-(aminoacetyl)serine" EXACT RESID-alternate []
-synonym: "serine glycinate ester" EXACT RESID-alternate []
-synonym: "CROSSLNK Glycyl serine ester (Ser-Gly) (interchain with G-...)" EXACT UniProt-feature []
-synonym: "CROSSLNK Glycyl serine ester (Gly-Ser) (interchain with S-...)" EXACT UniProt-feature []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 5 H 7 N 2 O 3" xsd:string
-property_value: MassAvg "143.12" xsd:float
-property_value: MassMono "143.045667" xsd:float
-property_value: Origin "G, S" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0422
-is_a: MOD:00885
-is_a: MOD:02047
-is_a: MOD:02055
-is_a: MOD:00954
-
-[Term]
-id: MOD:01586
-name: O-glycyl-L-threonine
-def: "A protein modification that effectively crosslinks an L-threonine residue and a glycine residue by an ester bond to form O-glycyl-L-threonine." [PubMed:17502423, RESID:AA0496]
-comment: Cross-link 2.
-synonym: "(2S,3R)-2-amino-3-[(aminoacetyl)oxy]butanoic acid" EXACT RESID-systematic []
-synonym: "O-(glycyl)-L-threonine" EXACT RESID-name []
-synonym: "O3-(2-aminoacetyl)threonine" EXACT RESID-alternate []
-synonym: "threonine glycinate ester" EXACT RESID-alternate []
-synonym: "CROSSLNK Glycyl threonine ester (Thr-Gly) (interchain with G-...)" EXACT UniProt-feature []
-synonym: "CROSSLNK Glycyl threonine ester (Gly-Thr) (interchain with T-...)" EXACT UniProt-feature []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 6 H 9 N 2 O 3" xsd:string
-property_value: MassAvg "157.15" xsd:float
-property_value: MassMono "157.061317" xsd:float
-property_value: Origin "G, T" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0423
-is_a: MOD:00885
-is_a: MOD:02047
-is_a: MOD:00917
-is_a: MOD:00954
-
-[Term]
-id: MOD:01587
-name: O-(2-aminoethylphosphoryl)-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O-(2-aminoethylphosphoryl)-L-serine." [PubMed:15249686, PubMed:16825186, PubMed:16949362, RESID:AA0497]
-synonym: "(2S)-2-amino-3-([(2-aminoethoxy)(hydroxy)phosphoryl]oxy)propanoic acid" EXACT RESID-systematic []
-synonym: "MOD_RES O-(2-aminoethylphosphoryl)serine" EXACT UniProt-feature []
-synonym: "O-(2-aminoethylphosphoryl)-L-serine" EXACT RESID-name []
-synonym: "O3-(2-aminoethylphosphoryl)-L-serine" EXACT RESID-alternate []
-synonym: "O3-(phosphoethanolamine)-L-serine" EXACT RESID-alternate []
-synonym: "serine ethanolamine phosphate" EXACT RESID-alternate []
-synonym: "serine ethanolamine phosphodiester" EXACT RESID-alternate []
-property_value: DiffAvg "123.05" xsd:float
-property_value: DiffFormula "C 2 H 6 N 1 O 3 P 1" xsd:string
-property_value: DiffMono "123.008530" xsd:float
-property_value: Formula "C 5 H 11 N 2 O 5 P 1" xsd:string
-property_value: MassAvg "210.13" xsd:float
-property_value: MassMono "210.040558" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0399
-is_a: MOD:00861
-is_a: MOD:00916
-
-[Term]
-id: MOD:01588
-name: O-cholinephosphoryl-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O-cholinephosphoryl-L-serine." [PubMed:15249686, PubMed:16825186, PubMed:16949362, RESID:AA0498]
-synonym: "2-[([(2S)-2-amino-2-carboxyethoxy][hydroxy]phosphoryl)oxy]-N,N,N-trimethylethanaminium" EXACT RESID-systematic []
-synonym: "2-[([(2S)-2-azanyl-2-carboxyethoxy][hydroxy]phosphoryl)oxy]-N,N,N-trimethylethanazanium" EXACT RESID-alternate []
-synonym: "MOD_RES O-(2-cholinephosphoryl)serine" EXACT UniProt-feature []
-synonym: "O-cholinephosphoryl-L-serine" EXACT RESID-name []
-synonym: "O3-[(2-[trimethylammonio]ethyl)phosphoryl]-L-serine" EXACT RESID-alternate []
-synonym: "O3-phosphocholine-L-serine" EXACT RESID-alternate []
-synonym: "serine choline phosphate" EXACT RESID-alternate []
-synonym: "serine choline phosphodiester" EXACT RESID-alternate []
-property_value: DiffAvg "166.14" xsd:float
-property_value: DiffFormula "C 5 H 13 N 1 O 3 P 1" xsd:string
-property_value: DiffMono "166.062756" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 8 H 18 N 2 O 5 P 1" xsd:string
-property_value: MassAvg "253.21" xsd:float
-property_value: MassMono "253.094785" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0400
-is_a: MOD:00861
-is_a: MOD:00916
-
-[Term]
-id: MOD:01589
-name: O-(2,4-diacetamido-2,4-dideoxyglucosyl)-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O-(2,4-diacetamido-2,4-dideoxyglucosyl)-L-serine." [PubMed:15249686, PubMed:16949362, RESID:AA0499]
-synonym: "(2S)-2-amino-3-[(2,4-diacetamido-2,4-dideoxy-beta-D-glucopyranosyl)oxy]propanoic acid" EXACT RESID-systematic []
-synonym: "DADDGlc" EXACT RESID-alternate []
-synonym: "O-(2,4-diacetamido-2,4-dideoxy-beta-D-glucopyranosyl)-L-serine" EXACT RESID-alternate []
-synonym: "O-(2,4-diacetamido-2,4-dideoxy-D-glucosyl)-L-serine" EXACT RESID-name []
-synonym: "O-[2,4-bis(acetylamino)]glucosyl-L-serine" EXACT RESID-alternate []
-synonym: "O-seryl-beta-2,4-bis(acetylamino)glucoside" EXACT RESID-alternate []
-synonym: "O3-(2,4-diacetamido-2,4-dideoxy-beta-D-glucopyranosyl)-L-serine" EXACT RESID-alternate []
-synonym: "CARBOHYD O-linked (DADDGlc) serine" EXACT UniProt-feature []
-property_value: DiffAvg "244.25" xsd:float
-property_value: DiffFormula "C 10 H 16 N 2 O 5" xsd:string
-property_value: DiffMono "244.105922" xsd:float
-property_value: Formula "C 13 H 21 N 3 O 7" xsd:string
-property_value: MassAvg "331.33" xsd:float
-property_value: MassMono "331.137950" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0547
-is_a: MOD:00002
-
-[Term]
-id: MOD:01590
-name: 3'-farnesyl-2',3'-dihydro-2',N2-cyclo-L-tryptophan
-def: "A protein modification that effectively converts an L-tryptophan residue to 3'-farnesyl-2',3'-dihydro-2',N2-cyclo-L-tryptophan." [ChEBI:52950, PubMed:18323630, RESID:AA0500]
-synonym: "(2S,3aR,8aS)-3a-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]-1,2,3,3a,8,8a-hexahydropyrrolo[2,3-b]indole-2-carboxylic acid" EXACT RESID-systematic []
-synonym: "3'-farnesyl-2',3'-dihydro-2',N2-cyclo-L-tryptophan" EXACT RESID-name []
-synonym: "LIPID 3'-farnesyl-2',N2-cyclotryptophan" EXACT UniProt-feature []
-property_value: DiffAvg "204.36" xsd:float
-property_value: DiffFormula "C 15 H 24 N 0 O 0" xsd:string
-property_value: DiffMono "204.187801" xsd:float
-property_value: Formula "C 26 H 34 N 2 O 1" xsd:string
-property_value: MassAvg "390.57" xsd:float
-property_value: MassMono "390.267114" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00437
-is_a: MOD:00601
-is_a: MOD:01115
-
-[Term]
-id: MOD:01591
-name: modifications with monoisotopic mass differences that are nominally equal at 304.205359 Da
-def: "Modifications that have monoisotopic mass differences from their respective origins of 304.205359 Da." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:01515
-is_a: MOD:01592
-
-[Term]
-id: MOD:01592
-name: modifications with monoisotopic mass differences that are nominally equal at 304.199-304.206 Da
-def: "Modifications that have monoisotopic mass differences from their respective origins of 304.199-304.206 Da." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:01514
-
-[Term]
-id: MOD:01593
-name: iTRAQ8plex reporter fragment
-def: "A protein modification reporter fragment produced by an Applied Biosystems iTRAQ8plex reagent derivatized residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "4-methyl-1-methylidenepiperazin-1-ium" EXACT PSI-MOD-alternate []
-is_a: MOD:01520
-
-[Term]
-id: MOD:01594
-name: iTRAQ8plex-113 reporter fragment
-def: "The protein modification reporter fragment produced by an Applied Biosystems iTRAQ8plex-113 reagent derivatized residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "4-methyl-1-methylidenepiperazin-1-ium" EXACT PSI-MOD-alternate []
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "(12)C 6 H 13 (14)N 2" xsd:string
-property_value: MassAvg "113.11" xsd:float
-property_value: MassMono "113.107325" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01593
-relationship: derives_from MOD:01528
-
-[Term]
-id: MOD:01595
-name: iTRAQ8plex-114 reporter fragment
-def: "The protein modification reporter fragment produced by an Applied Biosystems iTRAQ8plex-114 reagent derivatized residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "4-methyl-1-methylidenepiperazin-1-ium" EXACT PSI-MOD-alternate []
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "(12)C 5 (13)C 1 H 13 (14)N 2" xsd:string
-property_value: MassAvg "114.11" xsd:float
-property_value: MassMono "114.110680" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01593
-relationship: derives_from MOD:01535
-
-[Term]
-id: MOD:01596
-name: iTRAQ8plex-115 reporter fragment
-def: "The protein modification reporter fragment produced by an Applied Biosystems iTRAQ8plex-115 reagent derivatized residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "4-methyl-1-methylidenepiperazin-1-ium" EXACT PSI-MOD-alternate []
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "(12)C 5 (13)C 1 H 13 (14)N 1 (15)N 1" xsd:string
-property_value: MassAvg "115.11" xsd:float
-property_value: MassMono "115.107715" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01593
-relationship: derives_from MOD:01542
-
-[Term]
-id: MOD:01597
-name: iTRAQ8plex-116 reporter fragment
-def: "The protein modification reporter fragment produced by an Applied Biosystems iTRAQ8plex-116 reagent derivatized residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "4-methyl-1-methylidenepiperazin-1-ium" EXACT PSI-MOD-alternate []
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "(12)C 4 (13)C 2 H 13 (14)N 1 (15)N 1" xsd:string
-property_value: MassAvg "116.11" xsd:float
-property_value: MassMono "116.111069" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01593
-relationship: derives_from MOD:01549
-
-[Term]
-id: MOD:01598
-name: iTRAQ8plex-117 reporter fragment
-def: "The protein modification reporter fragment produced by an Applied Biosystems iTRAQ8plex-117 reagent derivatized residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "4-methyl-1-methylidenepiperazin-1-ium" EXACT PSI-MOD-alternate []
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "(12)C 3 (13)C 3 H 13 (14)N 1 (15)N 1" xsd:string
-property_value: MassAvg "117.11" xsd:float
-property_value: MassMono "117.114424" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01593
-relationship: derives_from MOD:01556
-
-[Term]
-id: MOD:01599
-name: iTRAQ8plex-118 reporter fragment
-def: "The protein modification reporter fragment produced by an Applied Biosystems iTRAQ8plex-118 reagent derivatized residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "4-methyl-1-methylidenepiperazin-1-ium" EXACT PSI-MOD-alternate []
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "(12)C 3 (13)C 3 H 13 (15)N 2" xsd:string
-property_value: MassAvg "118.11" xsd:float
-property_value: MassMono "118.111459" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01593
-relationship: derives_from MOD:01563
-
-[Term]
-id: MOD:01600
-name: iTRAQ8plex-119 reporter fragment
-def: "The protein modification reporter fragment produced by an Applied Biosystems iTRAQ8plex-119 reagent derivatized residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "4-methyl-1-methylidenepiperazin-1-ium" EXACT PSI-MOD-alternate []
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "(12)C 2 (13)C 4 H 13 (15)N 2" xsd:string
-property_value: MassAvg "119.11" xsd:float
-property_value: MassMono "119.114814" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01593
-relationship: derives_from MOD:01570
-
-[Term]
-id: MOD:01601
-name: iTRAQ8plex-121 reporter fragment
-def: "The protein modification reporter fragment produced by an Applied Biosystems iTRAQ8plex-121 reagent derivatized residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "4-methyl-1-methylidenepiperazin-1-ium" EXACT PSI-MOD-alternate []
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "(13)C 6 H 13 (15)N 2" xsd:string
-property_value: MassAvg "121.12" xsd:float
-property_value: MassMono "121.121524" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01593
-relationship: derives_from MOD:01577
-
-[Term]
-id: MOD:01602
-name: S-(L-lysyl)-L-methionine sulfilimine
-def: "A protein modification that effectively converts an L-lysine residue, and an L-methionine residue to S-(L-lysyl)-L-methionine sulfilimine." [PubMed:12011424, PubMed:15951440, PubMed:19729652, RESID:AA0501]
-comment: Cross-link 2.
-synonym: "(2S)-2-amino-6-([(E)-[(3S)-3-amino-3-carboxypropyl](methyl)-lambda(4)-sulfanylidene]amino)hexanoic acid" EXACT RESID-systematic []
-synonym: "(E)-N6-([(3S)-3-amino-3-carboxypropyl](methyl)-lambda(4)-sulfanylidene)-L-lysine" EXACT RESID-alternate []
-synonym: "S-(L-lysyl)-L-methionine sulfilimine" EXACT RESID-name []
-synonym: "S-lysyl-methionine" EXACT RESID-alternate []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 11 H 19 N 3 O 2 S 1" xsd:string
-property_value: MassAvg "257.35" xsd:float
-property_value: MassMono "257.119798" xsd:float
-property_value: Origin "K, M" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0401
-is_a: MOD:02051
-is_a: MOD:02052
-
-[Term]
-id: MOD:01603
-name: 2x(15)N labeled L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to 2x(15)N labeled L-lysine." [PubMed:18688235, URL:http\://www.sigmaaldrich.com/catalog/ProductDetail.do?N4=609021|ALDRICH&N5=SEARCH_CONCAT_PNO|BRAND_KEY&F=SPEC&lang=en_US0.000000E+000]
-subset: PSI-MOD-slim
-property_value: DiffAvg "1.99" xsd:float
-property_value: DiffFormula "(14)N -2 (15)N 2" xsd:string
-property_value: DiffMono "1.994070" xsd:float
-property_value: Formula "C 6 H 12 (15)N 2 O 1" xsd:string
-property_value: MassAvg "130.09" xsd:float
-property_value: MassMono "130.089033" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:995
-is_a: MOD:00843
-is_a: MOD:00912
-
-[Term]
-id: MOD:01604
-name: 4x(15)N labeled L-arginine
-def: "A protein modification that effectively converts an L-arginine residue to 4x(15)N labeled L-arginine." [PubMed:18688235, URL:http\://www.sigmaaldrich.com/catalog/ProductDetail.do?N4=600113|ALDRICH&N5=SEARCH_CONCAT_PNO|BRAND_KEY&F=SPEC&lang=en_US0.000000E+000]
-subset: PSI-MOD-slim
-property_value: DiffAvg "3.99" xsd:float
-property_value: DiffFormula "(14)N -4 (15)N 4" xsd:string
-property_value: DiffMono "3.988140" xsd:float
-property_value: Formula "C 6 H 12 (15)N 4 O 1" xsd:string
-property_value: MassAvg "160.09" xsd:float
-property_value: MassMono "160.089251" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00843
-is_a: MOD:00902
-
-[Term]
-id: MOD:01605
-name: 5-glutamyl 2-aminoadipic acid
-def: "A protein modification that effectively converts an L-glutamic acid residue to 5-glutamyl 2-aminoadipic acid." [PubMed:19620981, RESID:AA0502, ChEBI:78503]
-synonym: "(2S)-2-([(4S)-4-amino-4-carboxybutanoyl]amino)hexanedioic acid" EXACT RESID-systematic []
-synonym: "5-glutamyl 2-aminoadipic acid" EXACT RESID-name []
-synonym: "MOD_RES 5-glutamyl 2-aminoadipic acid" EXACT UniProt-feature []
-synonym: "N2-(gamma-glutamyl)-2-aminoadipic acid" EXACT RESID-alternate []
-synonym: "N2-(isoglutamyl)-2-aminoadipic acid" EXACT RESID-alternate []
-property_value: DiffAvg "143.14" xsd:float
-property_value: DiffFormula "C 6 H 9 N 1 O 3" xsd:string
-property_value: DiffMono "143.058243" xsd:float
-property_value: Formula "C 11 H 16 N 2 O 6" xsd:string
-property_value: MassAvg "272.26" xsd:float
-property_value: MassMono "272.100836" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0406
-is_a: MOD:00906
-
-[Term]
-id: MOD:01606
-name: 5-glutamyl 2-aminoadipic 6-phosphoric anhydride
-def: "A protein modification that effectively converts an L-glutamic acid residue to 5-glutamyl 2-aminoadipic 6-phosphoric anhydride." [PubMed:19620981, RESID:AA0503]
-synonym: "(2S)-2-([(4S)-4-amino-4-carboxybutanoyl]amino)-6-oxo-6-(phosphonooxy)hexanoic acid" EXACT RESID-systematic []
-synonym: "5-glutamyl 2-aminoadipic 6-phosphoric anhydride" EXACT RESID-name []
-property_value: DiffAvg "223.12" xsd:float
-property_value: DiffFormula "C 6 H 10 N 1 O 6 P 1" xsd:string
-property_value: DiffMono "223.024574" xsd:float
-property_value: Formula "C 11 H 17 N 2 O 9 P 1" xsd:string
-property_value: MassAvg "352.24" xsd:float
-property_value: MassMono "352.067167" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "hypothetical" xsd:string
-is_a: MOD:00861
-is_a: MOD:00906
-
-[Term]
-id: MOD:01607
-name: 5-glutamyl allysine
-def: "A protein modification that effectively converts an L-glutamic acid residue to 5-glutamyl allysine." [PubMed:19620981, RESID:AA0504]
-synonym: "(2S)-2-([(4S)-4-amino-4-carboxybutanoyl]amino)-6-oxohexanoic acid" EXACT RESID-systematic []
-synonym: "2-(5-glutamyl)amino-6-oxohexanoic acid" EXACT RESID-alternate []
-synonym: "5-glutamyl allysine" EXACT RESID-name []
-synonym: "alpha-(gamma-glutamyl)allysine" EXACT RESID-alternate []
-synonym: "N2-(gamma-glutamyl)allysine" EXACT RESID-alternate []
-synonym: "N2-(isoglutamyl)allysine" EXACT RESID-alternate []
-property_value: DiffAvg "127.14" xsd:float
-property_value: DiffFormula "C 6 H 9 N 1 O 2" xsd:string
-property_value: DiffMono "127.063329" xsd:float
-property_value: Formula "C 11 H 16 N 2 O 5" xsd:string
-property_value: MassAvg "256.26" xsd:float
-property_value: MassMono "256.105922" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "hypothetical" xsd:string
-is_a: MOD:00906
-
-[Term]
-id: MOD:01608
-name: N2-(L-isoglutamyl)-L-lysine
-def: "A protein modification that effectively converts an L-glutamic acid residue to N2-(L-isoglutamyl)-L-lysine. This is not an isopeptide cross-link." [PubMed:19620981, RESID:AA0505]
-synonym: "(2S)-6-amino-2-([(4S)-4-amino-4-carboxybutanoyl]amino)hexanoic acid" EXACT RESID-systematic []
-synonym: "5-glutamyl N2-lysine" EXACT RESID-alternate []
-synonym: "alpha-(gamma-glutamyl)lysine" EXACT RESID-alternate []
-synonym: "gamma-glutamyl N2-lysine" EXACT RESID-alternate []
-synonym: "MOD_RES 5-glutamyl N2-lysine" EXACT UniProt-feature []
-synonym: "N2-(gamma-glutamyl)lysine" EXACT RESID-alternate []
-synonym: "N2-(L-isoglutamyl)-L-lysine" EXACT RESID-name []
-property_value: DiffAvg "128.18" xsd:float
-property_value: DiffFormula "C 6 H 12 N 2 O 1" xsd:string
-property_value: DiffMono "128.094963" xsd:float
-property_value: Formula "C 11 H 19 N 3 O 4" xsd:string
-property_value: MassAvg "257.29" xsd:float
-property_value: MassMono "257.137556" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0407
-is_a: MOD:00906
-
-[Term]
-id: MOD:01609
-name: 7'-hydroxy-2'-alpha-mannosyl-L-tryptophan
-def: "A protein modification that effectively converts an L-tryptophan residue to 7'-hydroxy-2'-alpha-mannosyl-L-tryptophan." [PubMed:19584055, RESID:AA0506]
-synonym: "(2S)-2-amino-3-[7-hydroxy-2-(alpha-D-mannopyranosyl)-1H-indol-3-yl]propanoic acid" EXACT RESID-systematic []
-synonym: "7'-hydroxy-2'-alpha-mannosyl-L-tryptophan" EXACT RESID-name []
-synonym: "CARBOHYD C-linked (Man) hydroxytryptophan" EXACT UniProt-feature []
-property_value: DiffAvg "178.14" xsd:float
-property_value: DiffFormula "C 6 H 10 N 0 O 6" xsd:string
-property_value: DiffMono "178.047738" xsd:float
-property_value: Formula "C 17 H 20 N 2 O 7" xsd:string
-property_value: MassAvg "364.35" xsd:float
-property_value: MassMono "364.127051" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0504
-is_a: MOD:00918
-relationship: has_functional_parent MOD:00222
-relationship: has_functional_parent MOD:01664
-
-[Term]
-id: MOD:01610
-name: L-threonine methyl ester
-def: "A protein modification that effectively converts an L-threonine residue to L-threonine methyl ester." [PubMed:19745839, RESID:AA0507]
-synonym: "L-threonine methyl ester" EXACT RESID-name []
-synonym: "methyl (2S,3R)-2-amino-3-hydroxybutanoate" EXACT RESID-systematic []
-synonym: "methyl L-threoninate" EXACT RESID-alternate []
-synonym: "MOD_RES Threonine methyl ester" EXACT UniProt-feature []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 5 H 10 N 1 O 3" xsd:string
-property_value: MassAvg "132.14" xsd:float
-property_value: MassMono "132.066068" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0412
-is_a: MOD:01689
-is_a: MOD:01803
-
-[Term]
-id: MOD:01611
-name: 6-(S-L-cysteinyl)-8alpha-(-3'-L-histidino)-FMN
-def: "A protein modification that crosslinks a cysteine and a histidine residue by forming the adduct 6-(S-L-cysteinyl)-8alpha-(-3'-L-histidino)-FMN." [PubMed:17935335, RESID:AA0508]
-comment: Cross-link 2.
-subset: PSI-MOD-slim
-synonym: "6-((R)-2-amino-2-carboxyethyl)sulfanyl-8alpha-[4-((S)-2-amino-2-carboxyethyl)imidazol-3-yl]-riboflavin 5'-trihydrogen phosphate" EXACT RESID-systematic []
-synonym: "6-(S-cysteinyl)-8alpha-(N(delta)-histidyl)-FMN" EXACT RESID-alternate []
-synonym: "6-(S-cysteinyl)-8alpha-(N(pi)-histidyl)-FMN" EXACT RESID-alternate []
-synonym: "6-(S-cysteinyl)-8alpha-(N3'-histidyl)-FMN" EXACT RESID-alternate []
-synonym: "6-(S-cysteinyl)-8alpha-(pros-histidyl)-FMN" EXACT RESID-alternate []
-synonym: "6-(S-L-cysteinyl)-8alpha-(N3'-L-histidino)-FMN" EXACT RESID-name []
-synonym: "BINDING FMN (covalent; via 2 links)" EXACT UniProt-feature []
-synonym: "BINDING FMN (covalent; via 2 links, pros nitrogen)" EXACT UniProt-feature []
-property_value: DiffAvg "452.32" xsd:float
-property_value: DiffFormula "C 17 H 17 N 4 O 9 P 1 S 0" xsd:string
-property_value: DiffMono "452.073315" xsd:float
-property_value: Formula "C 26 H 29 N 8 O 11 P 1 S 1" xsd:string
-property_value: MassAvg "692.60" xsd:float
-property_value: MassMono "692.141411" xsd:float
-property_value: Origin "C, H" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:02044
-is_a: MOD:02048
-is_a: MOD:01621
-
-[Term]
-id: MOD:01612
-name: 3'-iodo-L-tyrosine
-def: "A protein modification that effectively converts an L-tyrosine residue to 3'-iodo-L-tyrosine." [ChEBI:27847, PubMed:8995307, RESID:AA0509]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-(4-hydroxy-3-iodophenyl)propanoic acid" EXACT RESID-systematic []
-synonym: "3'-iodo-L-tyrosine" EXACT RESID-name []
-synonym: "3-iodo-L-tyrosine" EXACT RESID-alternate []
-synonym: "3-iodotyrosine" EXACT RESID-alternate []
-synonym: "4-hydroxy-3-iodo-phenylalanine" EXACT RESID-alternate []
-synonym: "MIT" EXACT RESID-alternate []
-synonym: "MOD_RES Iodotyrosine" EXACT UniProt-feature []
-property_value: DiffAvg "125.90" xsd:float
-property_value: DiffFormula "C 0 H -1 I 1 N 0 O 0" xsd:string
-property_value: DiffMono "125.896648" xsd:float
-property_value: Formula "C 9 H 8 I 1 N 1 O 2" xsd:string
-property_value: MassAvg "289.07" xsd:float
-property_value: MassMono "288.959976" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0411
-is_a: MOD:01228
-
-[Term]
-id: MOD:01613
-name: 3',5'-diiodo-L-tyrosine
-def: "A protein modification that effectively converts an L-tyrosine residue to 3',5'-diiodo-L-tyrosine." [ChEBI:15768, PubMed:8995307, RESID:AA0510]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-(4-hydroxy-3,5-diiodophenyl)propanoic acid" EXACT RESID-systematic []
-synonym: "3',5'-diiodo-L-tyrosine" EXACT RESID-name []
-synonym: "3,5-diiodo-L-tyrosine" EXACT RESID-alternate []
-synonym: "3,5-diiodotyrosine" EXACT RESID-alternate []
-synonym: "DIT" EXACT RESID-alternate []
-synonym: "iodogorgoic acid" EXACT RESID-alternate []
-synonym: "MOD_RES Diiodotyrosine" EXACT UniProt-feature []
-property_value: DiffAvg "251.79" xsd:float
-property_value: DiffFormula "C 0 H -2 I 2 N 0 O 0" xsd:string
-property_value: DiffMono "251.793295" xsd:float
-property_value: Formula "C 9 H 7 I 2 N 1 O 2" xsd:string
-property_value: MassAvg "414.97" xsd:float
-property_value: MassMono "414.856624" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0408
-is_a: MOD:01140
-
-[Term]
-id: MOD:01614
-name: glycyl phospho-5'-adenosine
-def: "A protein modification that effectively converts a glycine residue to glycyl phospho-5'-adenosine." [PubMed:16388576, PubMed:9632726, RESID:AA0511]
-synonym: "(2-aminoacetyl)oxy-([(2R,3R,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxy-oxolan-2-yl]methoxy)phosphinic acid" EXACT RESID-alternate []
-synonym: "([(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxy-oxolan-2-yl]methoxy-hydroxy-phosphoryl)-2-aminoethanoate" EXACT RESID-alternate []
-synonym: "5'-adenylic-glyinate" EXACT RESID-alternate []
-synonym: "aminoacetyl [5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methyl hydrogen phosphate" EXACT RESID-systematic []
-synonym: "glycine monoanhydride with 5'-adenylic acid" EXACT RESID-alternate []
-synonym: "glycyl 5'-adenylate" EXACT RESID-alternate []
-synonym: "glycyl adenosine-5'-phosphate" EXACT RESID-alternate []
-synonym: "glycyl phospho-5'-adenosine" EXACT RESID-name []
-synonym: "glycyladenylate" EXACT RESID-alternate []
-synonym: "MOD_RES Glycyl adenylate" EXACT UniProt-feature []
-property_value: DiffAvg "329.21" xsd:float
-property_value: DiffFormula "C 10 H 12 N 5 O 6 P 1" xsd:string
-property_value: DiffMono "329.052520" xsd:float
-property_value: Formula "C 12 H 16 N 6 O 8 P 1" xsd:string
-property_value: MassAvg "403.27" xsd:float
-property_value: MassMono "403.076723" xsd:float
-property_value: Origin "G" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0409
-is_a: MOD:00908
-is_a: MOD:01165
-
-[Term]
-id: MOD:01615
-name: glycyl cysteine dithioester
-def: "A protein modification that effectively crosslinks an L-cysteine residue and a glycine residue by a dithioester bond to form glycyl cysteine dithioester." [PubMed:11438688, PubMed:16388576, RESID:AA0512]
-comment: Cross-link 2.
-synonym: "(2R)-2-amino-3-[(aminoacetyl)disulfanyl]propanoic acid" EXACT RESID-systematic []
-synonym: "2-(glycyldithio)alanine" EXACT RESID-alternate []
-synonym: "glycyl cysteine dithioester" EXACT RESID-name []
-synonym: "S-glycyl cysteine persulfide" EXACT RESID-alternate []
-synonym: "S-glycyl thiocysteine" EXACT RESID-alternate []
-synonym: "thioglycine cysteine disulfide" EXACT RESID-alternate []
-property_value: DiffAvg "14.05" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1 S 1" xsd:string
-property_value: DiffMono "13.961506" xsd:float
-property_value: Formula "C 5 H 7 N 2 O 2 S 2" xsd:string
-property_value: MassAvg "191.24" xsd:float
-property_value: MassMono "190.994894" xsd:float
-property_value: Origin "C, G" xsd:string
-property_value: Source "hypothetical" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0410
-is_a: MOD:00395
-is_a: MOD:02047
-is_a: MOD:00954
-
-[Term]
-id: MOD:01616
-name: trithiocystine
-def: "A protein modification that effectively cross-links two L-cysteine residues and adds three sulfur atoms to form trithiocystine." [PubMed:19438211, RESID:AA0513]
-comment: Cross-link 2.
-synonym: "(2R,2'R)-3,3'-pentasulfane-1,5-diylbis(2-aminopropanoic acid)" EXACT RESID-systematic []
-synonym: "3,3'-pentathiobisalanine" EXACT RESID-alternate []
-synonym: "bis(2-amino-2-carboxyethyl)pentasulfide" EXACT RESID-alternate []
-synonym: "trithiocystine" EXACT RESID-name []
-property_value: DiffAvg "94.16" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0 S 3" xsd:string
-property_value: DiffMono "93.900563" xsd:float
-property_value: Formula "C 6 H 8 N 2 O 2 S 5" xsd:string
-property_value: MassAvg "300.44" xsd:float
-property_value: MassMono "299.918933" xsd:float
-property_value: Origin "C, C" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0417
-is_a: MOD:01620
-
-[Term]
-id: MOD:01617
-name: O-(6-phosphomannosyl)-L-threonine
-def: "A protein modification that effectively converts an L-threonine residue to O-(6-phosphomannosyl)-L-threonine." [PubMed:20044576, RESID:AA0514]
-synonym: "(2S,3R)-2-amino-3-[6-phosphonooxy-alpha-D-mannopyranosyloxy]butanoic acid" EXACT RESID-systematic []
-synonym: "O-(6-phosphomannosyl)-L-threonine" EXACT RESID-name []
-synonym: "O3-(6-phosphomannosyl)threonine" EXACT RESID-alternate []
-synonym: "CARBOHYD O-linked (Man6P) threonine" EXACT UniProt-feature []
-property_value: DiffAvg "242.12" xsd:float
-property_value: DiffFormula "C 6 H 11 N 0 O 8 P 1" xsd:string
-property_value: DiffMono "242.019154" xsd:float
-property_value: Formula "C 10 H 18 N 1 O 10 P 1" xsd:string
-property_value: MassAvg "343.22" xsd:float
-property_value: MassMono "343.066832" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0596
-is_a: MOD:00005
-is_a: MOD:01804
-
-[Term]
-id: MOD:01618
-name: L-alanyl-L-isoaspartyl cyclopeptide
-def: "A protein modification that effectively converts an L-alaine residue and an L-asparagine residue to L-alanyl-L-isoaspartyl cyclopeptide." [PubMed:19928958, PubMed:3207697, RESID:AA0515]
-comment: Cross-link 2.
-synonym: "(2S,5S)-2-methyl-3,7-dioxo-1,4-diazepane-5-carboxylic acid" EXACT RESID-systematic []
-synonym: "1,4.2-anhydro(L-alanyl-L-aspartic acid)" EXACT RESID-alternate []
-synonym: "CROSSLNK Alanine isoaspartyl cyclopeptide (Ala-Asn)" EXACT UniProt-feature []
-synonym: "L-alanyl-L-isoaspartyl cyclopeptide" EXACT RESID-name []
-property_value: DiffAvg "-17.03" xsd:float
-property_value: DiffFormula "C 0 H -3 N -1 O 0" xsd:string
-property_value: DiffMono "-17.026549" xsd:float
-property_value: Formula "C 7 H 9 N 2 O 3" xsd:string
-property_value: MassAvg "169.16" xsd:float
-property_value: MassMono "169.061317" xsd:float
-property_value: Origin "A, N" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0418
-is_a: MOD:00688
-is_a: MOD:02040
-is_a: MOD:02042
-is_a: MOD:00946
-
-[Term]
-id: MOD:01619
-name: multisulfide crosslinked residues
-def: "A protein modification that crosslinks two cysteine residues by formation of a chain of two or more bonded sulfur atoms." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:00033
-is_a: MOD:02044
-
-[Term]
-id: MOD:01620
-name: polysulfide crosslinked residues
-def: "A protein modification that crosslinks two cysteine residues by formation of a chain of three or more bonded sulfur atoms." [PubMed:18688235]
-is_a: MOD:00860
-is_a: MOD:01619
-
-[Term]
-id: MOD:01621
-name: flavin crosslinked residues
-def: "A protein modification that crosslinks two or more amino acid residues by forming an adduct with a compound containing a flavin group." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:00033
-is_a: MOD:00697
-
-[Term]
-id: MOD:01622
-name: monohydroxylated tryptophan
-def: "A protein modification that effectively converts an L-tryptophan residue to one of several monohydroxylated tryptophan residues, including 3-hydroxy-L-tryptophan and 7'-hydroxy-L-tryptophan." [OMSSA:90, Unimod:35#W]
-synonym: "Oxidation" RELATED PSI-MS-label []
-synonym: "oxyw" EXACT OMSSA-label []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 11 H 10 N 2 O 2" xsd:string
-property_value: MassAvg "202.21" xsd:float
-property_value: MassMono "202.074228" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:35
-is_a: MOD:00425
-is_a: MOD:00918
-
-[Term]
-id: MOD:01623
-name: 1-thioglycine (C-terminal)
-def: "A protein modification that effectively converts a glycine residue to a C-terminal 1-thioglycine." [PubMed:11463785, PubMed:19145231, PubMed:9367957, RESID:AA0265#var]
-subset: PSI-MOD-slim
-property_value: DiffAvg "16.06" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O -1 S 1" xsd:string
-property_value: DiffMono "15.977156" xsd:float
-property_value: Formula "C 2 H 3 N 1 S 1" xsd:string
-property_value: MassAvg "73.11" xsd:float
-property_value: MassMono "72.998620" xsd:float
-property_value: Origin "G" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-is_a: MOD:01625
-
-[Term]
-id: MOD:01624
-name: (2-aminosuccinimidyl)acetic acid (Asn)
-def: "A protein modification that crosslinks an asparagine and the following glycine residue with the formation of (2-aminosuccinimidyl)acetic acid and the release of ammonia." [PubMed:10801322, PubMed:2015294, RESID:AA0441#ASN]
-comment: Cross-link 2.
-subset: PSI-MOD-slim
-synonym: "(2-aminosuccinimidyl)acetic acid" EXACT RESID-name []
-synonym: "(3-amino-2,5-dioxo-1-pyrrolidinyl)acetic acid" EXACT RESID-alternate []
-synonym: "[(3S)-3-amino-2,5-dioxopyrrolidin-1-yl]acetic acid" EXACT RESID-systematic []
-synonym: "anhydroaspartyl glycine" EXACT RESID-alternate []
-synonym: "aspartimide glycine" EXACT RESID-alternate []
-synonym: "CROSSLNK (2-aminosuccinimidyl)acetic acid (Asn-Gly)" EXACT UniProt-feature []
-synonym: "N-(2-aminosuccinyl)glycine" EXACT RESID-alternate []
-property_value: DiffAvg "-17.03" xsd:float
-property_value: DiffFormula "C 0 H -3 N -1 O 0" xsd:string
-property_value: DiffMono "-17.026549" xsd:float
-property_value: Formula "C 6 H 6 N 2 O 3" xsd:string
-property_value: MassAvg "154.13" xsd:float
-property_value: MassMono "154.037842" xsd:float
-property_value: Origin "G, N" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: uniprot.ptm:PTM-0450
-is_a: MOD:02042
-is_a: MOD:00946
-is_a: MOD:01628
-
-[Term]
-id: MOD:01625
-name: 1-thioglycine
-def: "A protein modification that effectively converts a glycine residue to 1-thioglycine." [PubMed:11463785, PubMed:9367957, RESID:AA0265]
-comment: This modification occurs naturally in two forms. At an interior peptide location (MOD:00270) it exists as aminoethanethionic acid, or aminoethanethioic O-acid. At the C-terminal (MOD:01623) it exists as aminoethanethiolic acid, or aminoethanethioic S-acid [JSG].
-subset: PSI-MOD-slim
-synonym: "1-thioglycine" EXACT RESID-name []
-synonym: "2-amino-1-sulfanylethanone" EXACT RESID-alternate []
-synonym: "aminoethanethioic acid" EXACT RESID-systematic []
-synonym: "aminothioacetic acid" EXACT RESID-alternate []
-synonym: "Carboxy->Thiocarboxy" RELATED PSI-MS-label []
-synonym: "MOD_RES 1-thioglycine" EXACT UniProt-feature []
-synonym: "S(O)Gly" EXACT PSI-MOD-label []
-synonym: "thiocarboxylic acid" RELATED Unimod-description []
-property_value: DiffAvg "16.06" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O -1 S 1" xsd:string
-property_value: DiffMono "15.977156" xsd:float
-property_value: Origin "G" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00749
-is_a: MOD:00908
-
-[Term]
-id: MOD:01626
-name: L-cystine
-def: "A protein modification that forms L-cystine by forming a disulfide bond that either cross-links two peptidyl L-cysteine residues, or modifies a peptidyl cysteine with a free cysteine." [ChEBI:16283, PubMed:1988019, PubMed:2001356, PubMed:2076469, PubMed:3083866, PubMed:366603, PubMed:7918467, PubMed:8344916, RESID:AA0025]
-comment: This modification occurs naturally in two forms. It exists as a disulfide cross-link of two cysteine residues (MOD:00034), or as a disulfide cross-link of a cysteine residues and a free cysteine (MOD:00765).
-subset: PSI-MOD-slim
-synonym: "(2R,2'R)-3,3'-disulfane-1,2-diylbis(2-aminopropanoic acid)" EXACT RESID-systematic []
-synonym: "2-amino-3-(2-amino-2-carboxy-ethyl)disulfanyl-propanoic acid" RELATED RESID-misnomer []
-synonym: "3,3'-disulfane-1,2-diylbis(2-azanylpropanoic acid)" EXACT RESID-alternate []
-synonym: "3,3'-dithiobis(2-aminopropanoic acid)" EXACT RESID-alternate []
-synonym: "3,3'-dithiobisalanine" EXACT RESID-alternate []
-synonym: "3,3'-dithiodialanine" EXACT RESID-alternate []
-synonym: "beta,beta'-diamino-beta,beta'-dicarboxydiethyldisulfide" EXACT RESID-alternate []
-synonym: "beta,beta'-dithiodialanine" EXACT RESID-alternate []
-synonym: "bis(alpha-aminopropionic acid)-beta-disulfide" EXACT RESID-alternate []
-synonym: "bis(beta-amino-beta-carboxyethyl)disulfide" EXACT RESID-alternate []
-synonym: "Cys2" EXACT PSI-MOD-label []
-synonym: "Cystine ((Cys)2)" EXACT DeltaMass-label []
-synonym: "dicysteine" EXACT RESID-alternate []
-synonym: "L-cystine" EXACT RESID-name []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Source "natural" xsd:string
-is_a: MOD:00905
-
-[Term]
-id: MOD:01627
-name: L-cysteinyl-L-selenocysteine
-def: "A protein modification that forms L-cysteinyl-L-selenocysteine either by the natural process of cross-linking an L-cysteine residue and an L-selenocysteine residue, or by the hypothetical process of substituting a selenium for a sulfur atom in cystine." [PubMed:12911312, PubMed:18688235]
-comment: Cross-link 2.
-subset: PSI-MOD-slim
-property_value: Formula "C 6 H 8 N 2 O 2 S 1 Se 1" xsd:string
-property_value: MassAvg "251.17" xsd:float
-property_value: MassMono "251.947170" xsd:float
-property_value: Origin "C, X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00692
-is_a: MOD:00859
-is_a: MOD:02044
-
-[Term]
-id: MOD:01628
-name: (2-aminosuccinimidyl)acetic acid
-def: "A protein modification that forms (2-aminosuccinimidyl)acetic acid by crosslinking either an aspartic acid residue or an asparagine residue with the following glycine residue." [PubMed:10801322, PubMed:18688235]
-comment: Cross-link 2; this cross-link is formed by the condensation of an aspartic acid residue or an asparagine residue with the alpha-amido of the following residue.
-subset: PSI-MOD-slim
-property_value: Formula "C 6 H 6 N 2 O 3" xsd:string
-property_value: MassAvg "154.13" xsd:float
-property_value: MassMono "154.037842" xsd:float
-property_value: Origin "G, X" xsd:string
-property_value: Source "hypothetical" xsd:string
-is_a: MOD:02047
-is_a: MOD:01944
-
-[Term]
-id: MOD:01629
-name: cyclo[(prolylserin)-O-yl] cysteinate
-def: "A protein modification that forms cyclo[(prolylserin)-O-yl] cysteinate by the natural process of cross-linking an L-cysteine residue an L-proline residue, and an L-serine residue, or by effectively modifying a cysteine residue." [PubMed:7961166, RESID:AA0489]
-synonym: "(3,6-dioxopyrrolo[4,5-a]piperazin-2-yl)methyl cysteinate" EXACT RESID-alternate []
-synonym: "[(3S,8aS)-1,4-dioxooctahydropyrrolo[1,2-a]pyrazin-3-yl]methyl (2R)-2-amino-3-sulfanylpropanoate" EXACT RESID-systematic []
-synonym: "cyclo[(prolylserin)-O-yl] cysteinate" EXACT RESID-name []
-synonym: "MOD_RES Cyclo[(prolylserin)-O-yl] cysteinate" EXACT UniProt-feature []
-property_value: Formula "C 11 H 16 N 3 O 4 S 1" xsd:string
-property_value: MassAvg "286.33" xsd:float
-property_value: MassMono "286.086152" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-is_a: MOD:00859
-is_a: MOD:02044
-
-[Term]
-id: MOD:01630
-name: N6-(L-isoglutamyl)-L-lysine
-def: "A protein modification that effectively crosslinks either an  L-glutamine residue or an L-glutamic acid residue with an L-lysine residue by an isopeptide bond to form  N6-(L-isoglutamyl)-L-lysine ." [ChEBI:21863, DeltaMass:0, PubMed:2461365, PubMed:5637041, PubMed:5656070, PubMed:8598899, RESID:AA0124]
-comment: Cross-link 2.
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-6-([(4S)-4-amino-4-carboxybutanoyl]amino)hexanoic acid" EXACT RESID-systematic []
-synonym: "2-azanyl-6-([4-azanyl-4-carboxybutanoyl]azanyl)hexanoic acid" EXACT RESID-alternate []
-synonym: "5-glutamyl N6-lysine" EXACT RESID-alternate []
-synonym: "N alpha -(gamma-Glutamyl)-lysine" EXACT DeltaMass-label []
-synonym: "N(epsilon)-(gamma-glutamyl)lysine" EXACT RESID-alternate []
-synonym: "N6-(L-isoglutamyl)-L-lysine" EXACT RESID-name []
-property_value: Formula "C 11 H 17 N 3 O 3" xsd:string
-property_value: MassAvg "239.27" xsd:float
-property_value: MassMono "239.126991" xsd:float
-property_value: Origin "K, X" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0397
-is_a: MOD:02051
-is_a: MOD:01875
-is_a: MOD:00688
-is_a: MOD:00859
-
-[Term]
-id: MOD:01631
-name: L-alanine removal
-def: "A protein modification that effectively removes or replaces an L-alanine." [PubMed:18688235]
-comment: This represents the loss or replacement of an L-alanine residue in a polypeptide, and may be combined with the formula or mass of another entry that is the replacement residue to represent a mutation or substitution.
-subset: PSI-MOD-slim
-property_value: DiffAvg "-71.08" xsd:float
-property_value: DiffFormula "C -3 H -5 N -1 O -1" xsd:string
-property_value: DiffMono "-71.037114" xsd:float
-property_value: Origin "A" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00901
-is_a: MOD:01651
-
-[Term]
-id: MOD:01632
-name: L-arginine removal
-def: "A protein modification that effectively removes or replaces an L-arginine." [PubMed:18688235]
-comment: This represents the loss or replacement of an L-arginine residue in a polypeptide, and may be combined with the formula or mass of another entry that is the replacement residue to represent a mutation or substitution.
-subset: PSI-MOD-slim
-property_value: DiffAvg "-156.19" xsd:float
-property_value: DiffFormula "C -6 H -12 N -4 O -1" xsd:string
-property_value: DiffMono "-156.101111" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00902
-is_a: MOD:01651
-
-[Term]
-id: MOD:01633
-name: L-asparagine removal
-def: "A protein modification that effectively removes or replaces an L-asparagine." [PubMed:18688235]
-comment: This represents the loss or replacement of an L-asparagine residue in a polypeptide, and may be combined with the formula or mass of another entry that is the replacement residue to represent a mutation or substitution.
-subset: PSI-MOD-slim
-property_value: DiffAvg "-114.10" xsd:float
-property_value: DiffFormula "C -4 H -6 N -2 O -2" xsd:string
-property_value: DiffMono "-114.042927" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00903
-is_a: MOD:01651
-
-[Term]
-id: MOD:01634
-name: L-aspartic acid removal
-def: "A protein modification that effectively removes or replaces an L-aspartic acid." [PubMed:18688235]
-comment: This represents the loss or replacement of an L-aspartic acid residue in a polypeptide, and may be combined with the formula or mass of another entry that is the replacement residue to represent a mutation or substitution.
-subset: PSI-MOD-slim
-property_value: DiffAvg "-115.09" xsd:float
-property_value: DiffFormula "C -4 H -5 N -1 O -3" xsd:string
-property_value: DiffMono "-115.026943" xsd:float
-property_value: Origin "D" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00904
-is_a: MOD:01651
-
-[Term]
-id: MOD:01635
-name: L-cysteine removal
-def: "A protein modification that effectively removes or replaces an L-cysteine." [PubMed:18688235]
-comment: This represents the loss or replacement of an L-cysteine residue in a polypeptide, and may be combined with the formula or mass of another entry that is the replacement residue to represent a mutation or substitution.
-subset: PSI-MOD-slim
-property_value: DiffAvg "-103.14" xsd:float
-property_value: DiffFormula "C -3 H -5 N -1 O -1 S -1" xsd:string
-property_value: DiffMono "-103.009185" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00905
-is_a: MOD:01651
-
-[Term]
-id: MOD:01636
-name: L-glutamic acid removal
-def: "A protein modification that effectively removes or replaces an L-glutamic acid." [PubMed:18688235]
-comment: This represents the loss or replacement of an L-glutamic acid residue in a polypeptide, and may be combined with the formula or mass of another entry that is the replacement residue to represent a mutation or substitution.
-subset: PSI-MOD-slim
-property_value: DiffAvg "-129.12" xsd:float
-property_value: DiffFormula "C -5 H -7 N -1 O -3" xsd:string
-property_value: DiffMono "-129.042593" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00906
-is_a: MOD:01651
-
-[Term]
-id: MOD:01637
-name: L-glutamine removal
-def: "A protein modification that effectively removes or replaces an L-glutamine." [PubMed:18688235]
-comment: This represents the loss or replacement of an L-glutamine residue in a polypeptide, and may be combined with the formula or mass of another entry that is the replacement residue to represent a mutation or substitution.
-subset: PSI-MOD-slim
-property_value: DiffAvg "-128.13" xsd:float
-property_value: DiffFormula "C -5 H -8 N -2 O -2" xsd:string
-property_value: DiffMono "-128.058578" xsd:float
-property_value: Origin "Q" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00907
-is_a: MOD:01651
-
-[Term]
-id: MOD:01638
-name: glycine removal
-def: "A protein modification that effectively removes or replaces a glycine." [PubMed:18688235]
-comment: This represents the loss or replacement of an glycine residue in a polypeptide, and may be combined with the formula or mass of another entry that is the replacement residue to represent a mutation or substitution.
-subset: PSI-MOD-slim
-property_value: DiffAvg "-57.05" xsd:float
-property_value: DiffFormula "C -2 H -3 N -1 O -1" xsd:string
-property_value: DiffMono "-57.021464" xsd:float
-property_value: Origin "G" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00908
-is_a: MOD:01651
-
-[Term]
-id: MOD:01639
-name: L-histidine removal
-def: "A protein modification that effectively removes or replaces an L-histidine." [PubMed:18688235]
-comment: This represents the loss or replacement of an L-histidine residue in a polypeptide, and may be combined with the formula or mass of another entry that is the replacement residue to represent a mutation or substitution.
-subset: PSI-MOD-slim
-property_value: DiffAvg "-137.14" xsd:float
-property_value: DiffFormula "C -6 H -7 N -3 O -1" xsd:string
-property_value: DiffMono "-137.058912" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00909
-is_a: MOD:01651
-
-[Term]
-id: MOD:01640
-name: L-isoleucine removal
-def: "A protein modification that effectively removes or replaces an L-isoleucine." [PubMed:18688235]
-comment: This represents the loss or replacement of an L-isoleucine residue in a polypeptide, and may be combined with the formula or mass of another entry that is the replacement residue to represent a mutation or substitution.
-subset: PSI-MOD-slim
-property_value: DiffAvg "-113.16" xsd:float
-property_value: DiffFormula "C -6 H -11 N -1 O -1" xsd:string
-property_value: DiffMono "-113.084064" xsd:float
-property_value: Origin "I" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00910
-is_a: MOD:01651
-
-[Term]
-id: MOD:01641
-name: L-leucine removal
-def: "A protein modification that effectively removes or replaces an L-leucine." [PubMed:18688235]
-comment: This represents the loss or replacement of an L-leucine residue in a polypeptide, and may be combined with the formula or mass of another entry that is the replacement residue to represent a mutation or substitution.
-subset: PSI-MOD-slim
-property_value: DiffAvg "-113.16" xsd:float
-property_value: DiffFormula "C -6 H -11 N -1 O -1" xsd:string
-property_value: DiffMono "-113.084064" xsd:float
-property_value: Origin "L" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00911
-is_a: MOD:01651
-
-[Term]
-id: MOD:01642
-name: L-lysine removal
-def: "A protein modification that effectively removes or replaces an L-lysine." [PubMed:18688235]
-comment: This represents the loss or replacement of an L-lysine residue in a polypeptide, and may be combined with the formula or mass of another entry that is the replacement residue to represent a mutation or substitution.
-subset: PSI-MOD-slim
-property_value: DiffAvg "-128.18" xsd:float
-property_value: DiffFormula "C -6 H -12 N -2 O -1" xsd:string
-property_value: DiffMono "-128.094963" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00912
-is_a: MOD:01651
-
-[Term]
-id: MOD:01643
-name: L-methionine removal
-def: "A protein modification that effectively removes or replaces an L-methionine." [OMSSA:9, PubMed:3327521, Unimod:765]
-comment: This represents the loss or replacement of an L-methionine residue in a polypeptide, including initiator methionine removal in eukaryotes. It may be combined with the formula or mass of another entry that is the replacement residue to represent a mutation or substitution [JSG].
-subset: PSI-MOD-slim
-synonym: "Met-loss" RELATED Unimod-interim []
-synonym: "ntermmcleave" EXACT OMSSA-label []
-property_value: DiffAvg "-131.19" xsd:float
-property_value: DiffFormula "C -5 H -9 N -1 O -1 S -1" xsd:string
-property_value: DiffMono "-131.040485" xsd:float
-property_value: Origin "M" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:765
-is_a: MOD:00913
-is_a: MOD:01651
-
-[Term]
-id: MOD:01644
-name: L-phenylalanine removal
-def: "A protein modification that effectively removes or replaces an L-phenylalanine." [PubMed:18688235]
-comment: This represents the loss or replacement of an L-phenylalanine residue in a polypeptide, and may be combined with the formula or mass of another entry that is the replacement residue to represent a mutation or substitution.
-subset: PSI-MOD-slim
-property_value: DiffAvg "-147.18" xsd:float
-property_value: DiffFormula "C -9 H -9 N -1 O -1" xsd:string
-property_value: DiffMono "-147.068414" xsd:float
-property_value: Origin "F" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00914
-is_a: MOD:01651
-
-[Term]
-id: MOD:01645
-name: L-proline removal
-def: "A protein modification that effectively removes or replaces an L-proline." [PubMed:18688235]
-comment: This represents the loss or replacement of an L-proline residue in a polypeptide, and may be combined with the formula or mass of another entry that is the replacement residue to represent a mutation or substitution.
-subset: PSI-MOD-slim
-property_value: DiffAvg "-97.12" xsd:float
-property_value: DiffFormula "C -5 H -7 N -1 O -1" xsd:string
-property_value: DiffMono "-97.052764" xsd:float
-property_value: Origin "P" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00915
-is_a: MOD:01651
-
-[Term]
-id: MOD:01646
-name: L-serine removal
-def: "A protein modification that effectively removes or replaces an L-serine." [PubMed:18688235]
-comment: This represents the loss or replacement of an L-serine residue in a polypeptide, and may be combined with the formula or mass of another entry that is the replacement residue to represent a mutation or substitution.
-subset: PSI-MOD-slim
-property_value: DiffAvg "-87.08" xsd:float
-property_value: DiffFormula "C -3 H -5 N -1 O -2" xsd:string
-property_value: DiffMono "-87.032028" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00916
-is_a: MOD:01651
-
-[Term]
-id: MOD:01647
-name: L-threonine removal
-def: "A protein modification that effectively removes or replaces an L-threonine." [PubMed:18688235]
-comment: This represents the loss or replacement of an L-threonine residue in a polypeptide, and may be combined with the formula or mass of another entry that is the replacement residue to represent a mutation or substitution.
-subset: PSI-MOD-slim
-property_value: DiffAvg "-101.10" xsd:float
-property_value: DiffFormula "C -4 H -7 N -1 O -2" xsd:string
-property_value: DiffMono "-101.047678" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00917
-is_a: MOD:01651
-
-[Term]
-id: MOD:01648
-name: L-tryptophan removal
-def: "A protein modification that effectively removes or replaces an L-tryptophan." [PubMed:18688235]
-comment: This represents the loss or replacement of an L-tryptophan residue in a polypeptide, and may be combined with the formula or mass of another entry that is the replacement residue to represent a mutation or substitution.
-subset: PSI-MOD-slim
-property_value: DiffAvg "-186.21" xsd:float
-property_value: DiffFormula "C -11 H -10 N -2 O -1" xsd:string
-property_value: DiffMono "-186.079313" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00918
-is_a: MOD:01651
-
-[Term]
-id: MOD:01649
-name: L-tyrosine removal
-def: "A protein modification that effectively removes or replaces an L-tyrosine." [PubMed:18688235]
-comment: This represents the loss or replacement of an L-tyrosine residue in a polypeptide, and may be combined with the formula or mass of another entry that is the replacement residue to represent a mutation or substitution.
-subset: PSI-MOD-slim
-property_value: DiffAvg "-163.18" xsd:float
-property_value: DiffFormula "C -9 H -9 N -1 O -2" xsd:string
-property_value: DiffMono "-163.063329" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00919
-is_a: MOD:01651
-
-[Term]
-id: MOD:01650
-name: L-valine removal
-def: "A protein modification that effectively removes or replaces an L-valine." [PubMed:18688235]
-comment: This represents the loss or replacement of an L-valine residue in a polypeptide, and may be combined with the formula or mass of another entry that is the replacement residue to represent a mutation or substitution.
-subset: PSI-MOD-slim
-property_value: DiffAvg "-99.13" xsd:float
-property_value: DiffFormula "C -5 H -9 N -1 O -1" xsd:string
-property_value: DiffMono "-99.068414" xsd:float
-property_value: Origin "V" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00920
-is_a: MOD:01651
-
-[Term]
-id: MOD:01651
-name: natural, standard, encoded residue removal
-def: "A protein modification that effectively removes a natural, standard, encoded residue." [PubMed:18688235]
-comment: This represents the loss of an encoded residue in a polypeptide.
-subset: PSI-MOD-slim
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00009
-is_a: MOD:01156
-
-[Term]
-id: MOD:01652
-name: sulfonyl halide reagent derivatized residue
-def: "A protein modification that is produced by formation of an adduct with a sulfonyl halide compound used as a reagent." [PubMed:18688235]
-comment: These reagents typically react with N6-amino group of lysine residues and a free alpha-amino group of a peptide.
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-
-[Term]
-id: MOD:01653
-name: dansyl chloride derivatized residue
-def: "A protein modification that is produced by formation of an adduct with 5-dimethylaminonaphthalene-1-sulfonyl chloride, dansyl chloride." [DeltaMass:0, Unimod:139]
-synonym: "5-dimethylaminonaphthalene-1-sulfonyl" RELATED Unimod-description []
-synonym: "Dansyl" RELATED PSI-MS-label []
-synonym: "Dansyl (Dns)" EXACT DeltaMass-label []
-synonym: "DansylRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "233.29" xsd:float
-property_value: DiffFormula "C 12 H 11 N 1 O 2 S 1" xsd:string
-property_value: DiffMono "233.051050" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:139
-is_a: MOD:01652
-
-[Term]
-id: MOD:01654
-name: N6-Dansyl derivatized lysine
-def: "A protein modification that is produced by reaction with 5-dimethylaminonaphthalene-1-sulfonyl chloride, dansyl chloride, to form N6-Dansyl-lysine." [Unimod:139#K]
-synonym: "5-dimethylaminonaphthalene-1-sulfonyl" RELATED Unimod-description []
-synonym: "Dansyl" RELATED PSI-MS-label []
-synonym: "N6DansylLys" EXACT PSI-MOD-label []
-property_value: DiffAvg "233.29" xsd:float
-property_value: DiffFormula "C 12 H 11 N 1 O 2 S 1" xsd:string
-property_value: DiffMono "233.051050" xsd:float
-property_value: Formula "C 18 H 23 N 3 O 3 S 1" xsd:string
-property_value: MassAvg "361.46" xsd:float
-property_value: MassMono "361.146013" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:139
-is_a: MOD:00912
-is_a: MOD:01653
-
-[Term]
-id: MOD:01655
-name: alpha-amino-Dansyl derivatized residue
-def: "A protein modification that is produced by reaction with 5-dimethylaminonaphthalene-1-sulfonyl chloride, dansyl chloride, to form an alpha-amino-Dansyl-derivatized residue." [Unimod:139#N-term]
-synonym: "5-dimethylaminonaphthalene-1-sulfonyl" RELATED Unimod-description []
-synonym: "Dansyl" RELATED PSI-MS-label []
-synonym: "N2DansylRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "233.29" xsd:float
-property_value: DiffFormula "C 12 H 11 N 1 O 2 S 1" xsd:string
-property_value: DiffMono "233.051050" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:139
-is_a: MOD:01653
-
-[Term]
-id: MOD:01656
-name: Dabsyl chloride derivatized residue
-def: "A protein modification that is produced by formation of an adduct with 4-(4-dimethylaminophenylazo)benzenesulfonyl chloride, Dabsyl chloride." [PubMed:18688235]
-synonym: "4-([4-(dimethylamino)phenyl]diazenyl)benzenesulfonyl" EXACT PSI-MOD-alternate []
-synonym: "DabsylRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "287.34" xsd:float
-property_value: DiffFormula "C 14 H 13 N 3 O 2 S 1" xsd:string
-property_value: DiffMono "287.072848" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01652
-
-[Term]
-id: MOD:01657
-name: N6-Dabsyl derivatized lysine
-def: "A protein modification that is produced by reaction with 4-(4-dimethylaminophenylazo)benzenesulfonyl chloride, dabsyl chloride, to form N6-Dabsyl-lysine." [PubMed:18688235]
-synonym: "N6-[4-([4-(dimethylamino)phenyl]diazenyl)benzenesulfonyl]lysine" EXACT PSI-MOD-alternate []
-synonym: "N6DabsylLys" EXACT PSI-MOD-label []
-property_value: DiffAvg "287.34" xsd:float
-property_value: DiffFormula "C 14 H 13 N 3 O 2 S 1" xsd:string
-property_value: DiffMono "287.072848" xsd:float
-property_value: Formula "C 20 H 25 N 5 O 3 S 1" xsd:string
-property_value: MassAvg "415.51" xsd:float
-property_value: MassMono "415.167811" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00912
-is_a: MOD:01656
-
-[Term]
-id: MOD:01658
-name: alpha-amino-Dabsyl derivatized residue
-def: "A protein modification that is produced by reaction with 4-(4-dimethylaminophenylazo)benzenesulfonyl chloride, dabsyl chloride, to form an alpha-amino-Dabsyl-derivatized residue." [PubMed:18688235]
-synonym: "N2DabsylRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "287.34" xsd:float
-property_value: DiffFormula "C 14 H 13 N 3 O 2 S 1" xsd:string
-property_value: DiffMono "287.072848" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:01656
-
-[Term]
-id: MOD:01659
-name: Uniblue A derivatized residue
-def: "A protein modification that is produced by formation of an adduct with 1-amino-4-{[3-(ethenylsulfonyl)phenyl]amino}-9,10-dioxo-9,10-dihydroanthracene-2-sulfonate, Uniblue A." [PubMed:18688235]
-comment: This reagent has a reactive sulfonyl vinyl and typically reacts with the free thiol group of cysteine residues.
-synonym: "1-amino-4-{[3-(ethenylsulfonyl)phenyl]amino}-9,10-dioxo-9,10-dihydroanthracene-2-sulfonic acid" EXACT PSI-MOD-alternate []
-synonym: "1-amino-9,10-dioxo-4-{[3-(vinylsulfonyl)phenyl]amino}-9,10-dihydroanthracene-2-sulfonic acid" EXACT PSI-MOD-alternate []
-synonym: "Uniblue A" EXACT PSI-MOD-alternate []
-synonym: "UniblueARes" EXACT PSI-MOD-label []
-property_value: DiffAvg "484.50" xsd:float
-property_value: DiffFormula "C 22 H 16 N 2 O 7 S 2" xsd:string
-property_value: DiffMono "484.039893" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-
-[Term]
-id: MOD:01660
-name: Uniblue A derivatized cysteine
-def: "A protein modification that is produced by reaction with 1-amino-4-{[3-(ethenylsulfonyl)phenyl]amino}-9,10-dioxo-9,10-dihydroanthracene-2-sulfonate, Uniblue A, to form Uniblue A cysteine adduct." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "1-amino-4-{[3-(ethenylsulfonyl)phenyl]amino}-9,10-dioxo-9,10-dihydroanthracene-2-sulfonate" EXACT PSI-MOD-alternate []
-synonym: "1-amino-9,10-dioxo-4-{[3-(vinylsulfonyl)phenyl]amino}-9,10-dihydroanthracene-2-sulfonate" EXACT PSI-MOD-alternate []
-synonym: "SUniblueACys" EXACT PSI-MOD-label []
-synonym: "Uniblue A" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "484.50" xsd:float
-property_value: DiffFormula "C 22 H 16 N 2 O 7 S 2" xsd:string
-property_value: DiffMono "484.039893" xsd:float
-property_value: Formula "C 25 H 21 N 3 O 8 S 3" xsd:string
-property_value: MassAvg "587.64" xsd:float
-property_value: MassMono "587.049078" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00905
-is_a: MOD:01659
-
-[Term]
-id: MOD:01661
-name: pyruvic acid (Tyr)
-def: "A protein modification that effectively converts an L-tyrosine residue to pyruvic acid." [PubMed:10085076, PubMed:3042771, PubMed:500639, PubMed:8464063, RESID:AA0127#TYR]
-synonym: "2-oxopropanoic acid" EXACT RESID-systematic []
-synonym: "MOD_RES Pyruvic acid (Tyr)" EXACT UniProt-feature []
-synonym: "pyruvic acid" EXACT RESID-name []
-property_value: DiffAvg "-93.13" xsd:float
-property_value: DiffFormula "C -6 H -7 N -1 O 0" xsd:string
-property_value: DiffMono "-93.057849" xsd:float
-property_value: Formula "C 3 H 3 O 2" xsd:string
-property_value: MassAvg "71.06" xsd:float
-property_value: MassMono "71.013304" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0662
-is_a: MOD:00919
-is_a: MOD:01154
-
-[Term]
-id: MOD:01662
-name: N5-(ADP-ribosyl)-L-glutamine
-def: "A protein modification that effectively converts an L-glutamine residue to N5-(ADP-ribosyl)-L-glutamine." [PubMed:20185726, RESID:AA0518]
-synonym: "(S)-2-amino-4-([adenosine 5'-(trihydrogen diphosphate) 5'->5'-ester with alpha-D-ribofuranosyl]amino)-5-oxopentanoic acid" EXACT RESID-systematic []
-synonym: "N5-(ADP-ribosyl)-L-glutamine" EXACT RESID-name []
-synonym: "N5-[alpha-D-ribofuranoside 5'->5'-ester with adenosine 5'-(trihydrogen diphosphate)]-L-glutamine" EXACT RESID-alternate []
-synonym: "N5-alpha-D-ribofuranosyl-L-glutamine 5'->5'-ester with adenosine 5'-(trihydrogen diphosphate)" EXACT RESID-alternate []
-property_value: DiffAvg "541.30" xsd:float
-property_value: DiffFormula "C 15 H 21 N 5 O 13 P 2" xsd:string
-property_value: DiffMono "541.061109" xsd:float
-property_value: Formula "C 20 H 29 N 7 O 15 P 2" xsd:string
-property_value: MassAvg "669.43" xsd:float
-property_value: MassMono "669.119687" xsd:float
-property_value: Origin "Q" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00752
-is_a: MOD:00907
-
-[Term]
-id: MOD:01663
-name: O-(ADP-ribosyl)-L-threonine
-def: "A protein modification that effectively converts an L-threonine residue to O-(ADP-ribosyl)-L-threonine." [PubMed:20185726, RESID:AA0519]
-synonym: "(S)-2-amino-3-([adenosine 5'-(trihydrogen diphosphate) 5'->5'-ester with alpha-D-ribofuranosyl]oxy)-butanoic acid" EXACT RESID-systematic []
-synonym: "O-(ADP-ribosyl)-L-threonine" EXACT RESID-name []
-synonym: "O3-(ADP-ribosyl)-L-threonine" EXACT RESID-alternate []
-synonym: "O3-[alpha-D-ribofuranoside 5'->5'-ester with adenosine 5'-(trihydrogen diphosphate)]-L-threonine" EXACT RESID-alternate []
-synonym: "O3-alpha-D-ribofuranosyl-L-threonine 5'->5'-ester with adenosine 5'-(trihydrogen diphosphate)" EXACT RESID-alternate []
-property_value: DiffAvg "541.30" xsd:float
-property_value: DiffFormula "C 15 H 21 N 5 O 13 P 2" xsd:string
-property_value: DiffMono "541.061109" xsd:float
-property_value: Formula "C 19 H 28 N 6 O 15 P 2" xsd:string
-property_value: MassAvg "642.41" xsd:float
-property_value: MassMono "642.108787" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00752
-is_a: MOD:00917
-
-[Term]
-id: MOD:01664
-name: 7'-hydroxy-L-tryptophan
-def: "A protein modification that effectively converts an L-tryptophan residue to a 7'-hydroxy-L-tryptophan." [PubMed:20223990, RESID:AA0520]
-synonym: "(2S)-2-amino-3-(7-hydroxy-1H-indol-3-yl)propanoic acid" EXACT RESID-systematic []
-synonym: "7'-hydroxy-L-tryptophan" EXACT RESID-name []
-synonym: "7-hydroxy-L-tryptophan" EXACT RESID-alternate []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 11 H 10 N 2 O 2" xsd:string
-property_value: MassAvg "202.21" xsd:float
-property_value: MassMono "202.074228" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0427
-is_a: MOD:01622
-
-[Term]
-id: MOD:01665
-name: N-(DNA-1',2'-dideoxyribos-1'-ylidene)-L-valine
-def: "A protein modification that effectively crosslinks an N-terminal L-valine residue and a strand of DNA at the C-1 of a ribose, freeing the nucleotide base and forming N-(DNA-1',2'-dideoxyribos-1'-ylidene)-L-valine." [PubMed:20185759, RESID:AA0521]
-synonym: "(2S)-2-[(3R,4R)-3,4-dihydroxy-5-(phosphonooxy)pentylidene]amino-3-methylbutanoic acid" EXACT RESID-systematic []
-synonym: "ACT_SITE Schiff-base intermediate with DNA; via amino nitrogen" EXACT UniProt-feature []
-synonym: "DNA glycosylase valine Schiff base intermediate" EXACT RESID-alternate []
-synonym: "N-(DNA-1',2'-dideoxyribos-1'-ylidene)-L-valine" EXACT RESID-name []
-property_value: Origin "V" xsd:string
-property_value: Source "hypothetical" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00750
-is_a: MOD:00920
-
-[Term]
-id: MOD:01666
-name: epicocconone derivatized residue
-def: "A protein modification that is produced by formation of an adduct with epicocconone." [PubMed:18688235]
-synonym: "(6S,9aS)-6-(hydroxymethyl)-3-[(1Z,4E,6E,8E)-1-hydroxy-3-oxodeca-1,4,6,8-tetraen-1-yl]-9a-methyl-5,6-dihydro-2H-furo[3,2-g]isochromene-2,9(9aH)-dione" EXACT PSI-MOD-alternate []
-synonym: "Deep Purple" EXACT PSI-MOD-alternate []
-synonym: "LavaPurple" EXACT PSI-MOD-alternate []
-synonym: "Lightning Fast" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "410.42" xsd:float
-property_value: DiffFormula "C 23 H 22 O 7" xsd:string
-property_value: DiffMono "410.136553" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-
-[Term]
-id: MOD:01667
-name: N6-epicoccononyl lysine adduct
-def: "A protein modification that is produced by formation of an adduct with epicocconone." [PubMed:18688235]
-synonym: "(6Z,7aS)-3-[(1Z,4E,6E,8E)-1-hydroxy-3-oxodeca-1,4,6,8-tetraen-1-yl]-7a-methyl-6-[([(1S)-1-amino-1-carboxylpentyl]amino)methylidene]-5-[(2S)-2,3-dihydroxypropyl]-1-benzofuran-2,7(6H,7aH)-dione" EXACT PSI-MOD-alternate []
-synonym: "DeepPurple" EXACT PSI-MOD-alternate []
-synonym: "LavaPurple" EXACT PSI-MOD-alternate []
-synonym: "Lightning Fast" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "410.42" xsd:float
-property_value: DiffFormula "C 23 H 22 O 7" xsd:string
-property_value: DiffMono "410.136553" xsd:float
-property_value: Formula "C 29 H 34 N 2 O 8" xsd:string
-property_value: MassAvg "538.60" xsd:float
-property_value: MassMono "538.231516" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00912
-is_a: MOD:01666
-
-[Term]
-id: MOD:01668
-name: O4-(8alpha-FAD)-L-aspartate
-def: "A protein modification that effectively converts an L-aspartic acid residue to O4-(8alpha-FAD)-L-aspartate." [PubMed:20080101, RESID:AA0522]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-4-oxo-4-[8alpha-riboflavin 5'-(trihydrogen diphosphate) 5'->5'-ester with adenosine]oxybutanoic acid" EXACT RESID-systematic []
-synonym: "8alpha-[(4-aspartyl)oxy]FAD" EXACT RESID-alternate []
-synonym: "O4-(8alpha-FAD)-L-aspartate" EXACT RESID-name []
-property_value: DiffAvg "783.54" xsd:float
-property_value: DiffFormula "C 27 H 31 N 9 O 15 P 2" xsd:string
-property_value: DiffMono "783.141485" xsd:float
-property_value: Formula "C 31 H 36 N 10 O 18 P 2" xsd:string
-property_value: MassAvg "898.63" xsd:float
-property_value: MassMono "898.168428" xsd:float
-property_value: Origin "D" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00895
-is_a: MOD:00904
-
-[Term]
-id: MOD:01669
-name: trimethyl-L-arginine
-def: "A protein modification that effectively converts an L-arginine residue to N(omega),N(omega),N'(omega)-trimethyl-L-arginine." [OMSSA:117, PubMed:11704273, PubMed:602668, RESID:AA0523, Unimod:37#R]
-synonym: "(2S)-2-amino-5-([(dimethylamino)(methylamino)methylidene]amino)pentanoic acid" EXACT RESID-systematic []
-synonym: "(2S)-2-amino-5-([(dimethylamino)(methylimino)methyl]amino)pentanoic acid" EXACT RESID-alternate []
-synonym: "2-[(4S)-4-amino-5-oxopentyl]-1,1,3-trimethylguanidine" EXACT RESID-alternate []
-synonym: "N(G)-trimethylarginine" EXACT RESID-alternate []
-synonym: "N5-[(dimethylamino)(imino)methyl]ornithine" EXACT RESID-alternate []
-synonym: "NoNoNo'Me3Arg" EXACT PSI-MOD-label []
-synonym: "omega-N,omega-N,omega-N'-trimethyl-L-arginine" EXACT RESID-name []
-synonym: "tri-Methylation" RELATED Unimod-description []
-synonym: "Trimethyl" RELATED PSI-MS-label []
-synonym: "trimethylationr" EXACT OMSSA-label []
-property_value: DiffAvg "42.08" xsd:float
-property_value: DiffFormula "C 3 H 6 N 0 O 0" xsd:string
-property_value: DiffMono "42.046950" xsd:float
-property_value: Formula "C 9 H 18 N 4 O 1" xsd:string
-property_value: MassAvg "198.27" xsd:float
-property_value: MassMono "198.148061" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: Unimod:37
-is_a: MOD:00430
-is_a: MOD:00602
-is_a: MOD:00658
-
-[Term]
-id: MOD:01670
-name: N6-chloro-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-methyl-L-lysine." [PubMed:16091367, PubMed:16195462, PubMed:17260957, RESID:AA0524]
-synonym: "(2S)-2-amino-6-(chloroamino)hexanoic acid" EXACT RESID-systematic []
-synonym: "epsilon-chlorolysine" EXACT RESID-alternate []
-synonym: "lysine chloramine" EXACT RESID-alternate []
-synonym: "N(zeta)-chlorolysine" EXACT RESID-alternate []
-synonym: "N6-chloro-L-lysine" EXACT RESID-name []
-synonym: "N6ClLys" EXACT PSI-MOD-label []
-property_value: DiffAvg "34.44" xsd:float
-property_value: DiffFormula "C 0 Cl 1 H -1 N 0 O 0" xsd:string
-property_value: DiffMono "33.961028" xsd:float
-property_value: Formula "C 6 Cl 1 H 11 N 2 O 1" xsd:string
-property_value: MassAvg "162.62" xsd:float
-property_value: MassMono "162.055991" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "hypothetical" xsd:string
-is_a: MOD:00912
-is_a: MOD:01672
-is_a: MOD:01911
-
-[Term]
-id: MOD:01671
-name: O-(L-isoaspartyl)-L-threonine (active site intermediate)
-def: "A protein modification that effectively converts an L-threonine residue to O-(L-isoaspartyl)-L-threonine, using free L-asparagine and releasing ammonia." [PubMed:8706862, RESID:AA0525#THR]
-comment: This is a threonine active intermediate and not an ester cross-link of peptides [JSG].
-synonym: "(2S)-2-amino-4-([(1S,2R)-1-amino-1-carboxypropan-2-yl]oxy)-4-oxobutanoic acid" EXACT RESID-systematic []
-synonym: "(2S,3R)-2-amino-3-([(4S)-3-amino-3-carboxypropanoyl]oxy)propanoic acid" EXACT RESID-alternate []
-synonym: "ACT_SITE O-isoaspartyl threonine intermediate" EXACT UniProt-feature []
-synonym: "O(beta)-(beta-aspartyl)threonine" EXACT RESID-alternate []
-synonym: "O-(L-isoaspartyl)-L-threonine" EXACT RESID-name []
-synonym: "O3-(isoaspartyl)-threonine" EXACT RESID-alternate []
-property_value: DiffAvg "115.09" xsd:float
-property_value: DiffFormula "C 4 H 5 N 1 O 3" xsd:string
-property_value: DiffMono "115.026943" xsd:float
-property_value: Formula "C 8 H 12 N 2 O 5" xsd:string
-property_value: MassAvg "216.19" xsd:float
-property_value: MassMono "216.074621" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00671
-is_a: MOD:01978
-
-[Term]
-id: MOD:01672
-name: halogenated lysine
-def: "A protein modification that effectively substitutes a hydrogen atom of an L-lysine residue with a halogen atom." [PubMed:18688235]
-property_value: Origin "K" xsd:string
-is_a: MOD:00694
-
-[Term]
-id: MOD:01673
-name: N-acetylaminohexosylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with an N-acetylaminohexose group through a glycosidic bond." [Unimod:43]
-subset: PSI-MOD-slim
-synonym: "HexNAc" RELATED PSI-MS-label []
-synonym: "HexNAcRes" EXACT PSI-MOD-label []
-synonym: "N-Acetylhexosamine" RELATED Unimod-description []
-property_value: DiffAvg "203.19" xsd:float
-property_value: DiffFormula "C 8 H 13 N 1 O 5" xsd:string
-property_value: DiffMono "203.079373" xsd:float
-property_value: Origin "X" xsd:string
-xref: Unimod:43
-is_a: MOD:00436
-
-[Term]
-id: MOD:01674
-name: N4-(N-acetylamino)hexosyl-L-asparagine
-def: "A protein modification that effectively converts an L-asparagine residue to N4-(N-acetaminohexosyl)-L-asparagine." [OMSSA:182, Unimod:43#N]
-subset: PSI-MOD-slim
-synonym: "(S)-2-amino-4-(2-acetamido-2-deoxy-beta-D-hexopyranosyl)amino-4-oxobutanoic acid" EXACT PSI-MOD-alternate []
-synonym: "HexNAc" RELATED PSI-MS-label []
-synonym: "HexNAcAsn" EXACT PSI-MOD-label []
-synonym: "hexNAcN" EXACT OMSSA-label []
-synonym: "N-Acetylhexosamine" RELATED Unimod-description []
-synonym: "N4-(2-acetamido-2-deoxy-beta-D-hexopyranosyl)-L-asparagine" EXACT PSI-MOD-alternate []
-synonym: "N4-(2-acetylamino-2-deoxy-beta-D-hexopyranosyl)-L-asparagine" EXACT PSI-MOD-alternate []
-synonym: "N4-(N-acetylhexosaminyl)asparagine" EXACT PSI-MOD-alternate []
-synonym: "N4-asparagine-beta-N-acetylhexosaminide" EXACT PSI-MOD-alternate []
-synonym: "N4-glycosyl-L-asparagine" EXACT PSI-MOD-alternate []
-synonym: "N4-glycosylasparagine" EXACT PSI-MOD-alternate []
-synonym: "N4HexNAcAsn" EXACT PSI-MOD-label []
-property_value: DiffAvg "203.19" xsd:float
-property_value: DiffFormula "C 8 H 13 N 1 O 5" xsd:string
-property_value: DiffMono "203.079373" xsd:float
-property_value: Formula "C 12 H 19 N 3 O 7" xsd:string
-property_value: MassAvg "317.30" xsd:float
-property_value: MassMono "317.122300" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:43
-is_a: MOD:00160
-is_a: MOD:01673
-
-[Term]
-id: MOD:01675
-name: O-(N-acetylamino)hexosyl-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O3-(N-acetylaminohexosyl)-L-serine." [OMSSA:184, Unimod:43#S]
-subset: PSI-MOD-slim
-synonym: "(S)-2-amino-3-(2-acetamido-2-deoxy-beta-D-hexopyranosyloxy)propanoic acid" EXACT PSI-MOD-alternate []
-synonym: "HexNAc" RELATED PSI-MS-label []
-synonym: "hexNAcS" EXACT OMSSA-label []
-synonym: "N-Acetylhexosamine" RELATED Unimod-description []
-synonym: "O-(2-acetylamino-2-deoxy-beta-D-hexopyranosyl)-L-serine" EXACT PSI-MOD-alternate []
-synonym: "O-(N-acetylhexosaminyl)serine" EXACT PSI-MOD-alternate []
-synonym: "O-glycosylserine" EXACT PSI-MOD-alternate []
-synonym: "O-seryl-beta-N-acetylhexosaminide" EXACT PSI-MOD-alternate []
-synonym: "O3-(2-acetamido-2-deoxy-beta-D-hexopyranosyl)-L-serine" EXACT PSI-MOD-alternate []
-synonym: "OHexNAcSer" EXACT PSI-MOD-label []
-property_value: DiffAvg "203.19" xsd:float
-property_value: DiffFormula "C 8 H 13 N 1 O 5" xsd:string
-property_value: DiffMono "203.079373" xsd:float
-property_value: Formula "C 11 H 18 N 2 O 7" xsd:string
-property_value: MassAvg "290.27" xsd:float
-property_value: MassMono "290.111401" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:43
-is_a: MOD:00002
-is_a: MOD:01673
-
-[Term]
-id: MOD:01676
-name: O-(N-acetylamino)hexosyl-L-threonine
-def: "A protein modification that effectively converts an L-threonine residue to O3-(N-acetylaminohexosyl)-L-threonine." [OMSSA:185, Unimod:43#T]
-subset: PSI-MOD-slim
-synonym: "(2S,3R)-2-amino-3-(alpha-D-2-acetamido-2-deoxyhexopyranosyloxy)butanoic acid" EXACT PSI-MOD-alternate []
-synonym: "HexNAc" RELATED PSI-MS-label []
-synonym: "hexNAcT" EXACT OMSSA-label []
-synonym: "N-Acetylhexosamine" RELATED Unimod-description []
-synonym: "O-(N-acetylhexcosaminyl)-L-threonine" EXACT PSI-MOD-alternate []
-synonym: "O-glycosylthreonine" EXACT PSI-MOD-alternate []
-synonym: "O3-(N-acetylhexosaminyl)threonine" EXACT PSI-MOD-alternate []
-synonym: "OHexNAcThr" EXACT PSI-MOD-label []
-property_value: DiffAvg "203.19" xsd:float
-property_value: DiffFormula "C 8 H 13 N 1 O 5" xsd:string
-property_value: DiffMono "203.079373" xsd:float
-property_value: Formula "C 12 H 20 N 2 O 7" xsd:string
-property_value: MassAvg "304.30" xsd:float
-property_value: MassMono "304.127051" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:43
-is_a: MOD:00005
-is_a: MOD:01673
-
-[Term]
-id: MOD:01677
-name: O4-(N-acetylamino)hexosyl-L-hydroxyproline
-def: "A protein modification that effectively converts an L-proline residue to O4-(N-acetylamino)hexosyl-L-hydroxyproline." [PubMed:18688235]
-comment: secondary to RESID:AA0030
-subset: PSI-MOD-slim
-synonym: "(2S,4R)-4-[2-acetamido-2-deoxy-alpha-D-hexopyranosyloxy]pyrrolidine-2-carboxylic acid" EXACT PSI-MOD-alternate []
-synonym: "4-(N-acetylhexosaminyloxy)proline" EXACT PSI-MOD-alternate []
-synonym: "4-[(2-N-acetylamino)-alpha-D-hexopyranosyl]oxyproline" EXACT PSI-MOD-alternate []
-synonym: "alpha-2-(N-acetylamino)hexopyranosyl-4-hydroxyproline" EXACT PSI-MOD-alternate []
-synonym: "HexNAc" RELATED PSI-MS-label []
-synonym: "O4-glycosyl-hydroxyproline" EXACT PSI-MOD-alternate []
-synonym: "O4HexNAcHyPro" EXACT PSI-MOD-label []
-property_value: DiffAvg "219.19" xsd:float
-property_value: DiffFormula "C 8 H 13 N 1 O 6" xsd:string
-property_value: DiffMono "219.074287" xsd:float
-property_value: Formula "C 13 H 20 N 2 O 7" xsd:string
-property_value: MassAvg "316.31" xsd:float
-property_value: MassMono "316.127051" xsd:float
-property_value: Origin "P" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00915
-relationship: contains MOD:01673
-
-[Term]
-id: MOD:01678
-name: N6-carbamoyl-L-lysine
-def: "A protein modification that effectively coverts L-lysine to N6-carbamoyl-L-lysine." [DeltaMass:56, OMSSA:31, PubMed:10978403, PubMed:12203680, Unimod:5#K, ChEBI:144369]
-comment: This modification can be produced by hydrogen cyanate, either as a reagent or as released by urea degradation in solution [JSG].
-subset: PSI-MOD-slim
-synonym: "2-amino-6-ureido-hexanoic acid" EXACT PSI-MOD-alternate []
-synonym: "Carbamyl" RELATED Unimod-interim []
-synonym: "Carbamylation" RELATED Unimod-description []
-synonym: "carbamylk" EXACT OMSSA-label []
-synonym: "homocitrulline" EXACT PSI-MOD-alternate []
-synonym: "N6-(aminocarbonyl)-L-lysine" EXACT PSI-MOD-alternate []
-synonym: "N6CbmLys" EXACT PSI-MOD-label []
-synonym: "MOD_RES N6-carbamoyllysine" EXACT UniProt-feature []
-property_value: DiffAvg "43.02" xsd:float
-property_value: DiffFormula "C 1 H 1 N 1 O 1" xsd:string
-property_value: DiffMono "43.005814" xsd:float
-property_value: Formula "C 7 H 13 N 3 O 2" xsd:string
-property_value: MassAvg "171.20" xsd:float
-property_value: MassMono "171.100777" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:5
-xref: uniprot.ptm:PTM-0675
-is_a: MOD:00912
-is_a: MOD:00398
-
-[Term]
-id: MOD:01679
-name: alpha-aminocarbamoylated residue
-def: "A protein modification that effectively replaces a residue alpha amino or imino hydrogen with a carbamoyl group." [DeltaMass:56, OMSSA:32, PubMed:10978403, PubMed:12203680, Unimod:5#N-term]
-comment: This modification can be produced by hydrogen cyanate, either as a reagent or as released by urea degradation. This modification effectively blocks Edman degradation, and because it can dehydrate to a cyanate group and react with another peptide N-terminal, it can effectively block two peptide molecules [JSG].
-subset: PSI-MOD-slim
-synonym: "Carbamyl" RELATED Unimod-interim []
-synonym: "Carbamylation" RELATED Unimod-description []
-synonym: "N2CbmRes" EXACT PSI-MOD-label []
-synonym: "ntermcarbamyl" EXACT OMSSA-label []
-property_value: DiffAvg "43.02" xsd:float
-property_value: DiffFormula "C 1 H 1 N 1 O 1" xsd:string
-property_value: DiffMono "43.005814" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:5
-is_a: MOD:00398
-
-[Term]
-id: MOD:01680
-name: alpha-amino monomethylated residue
-def: "A protein modification that effectively replaces one residue alpha amino or imino hydrogen with one methyl group." [OMSSA:11, OMSSA:76, Unimod:34#N-term]
-comment: Polypeptides with monomethylated amino terminals can undergo premature cleavage during the coupling step of an Edman degradation. This can result in \"preview\" with both a residue and the following residue being seen from the first step on through a sequence [JSG].
-subset: PSI-MOD-slim
-synonym: "Methyl" RELATED PSI-MS-label []
-synonym: "Methylation" RELATED Unimod-description []
-synonym: "N2Me1Res" EXACT PSI-MOD-label []
-synonym: "ntermmethyl" EXACT OMSSA-label []
-synonym: "ntermpepmethyl" EXACT OMSSA-label []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:34
-is_a: MOD:00599
-is_a: MOD:01460
-
-[Term]
-id: MOD:01681
-name: monomethylated L-aspartic acid
-def: "A protein modification that effectively replaces one hydrogen atom of an L-aspartic acid residue with one methyl group." [OMSSA:16, Unimod:34#D]
-synonym: "Me1Asp" EXACT PSI-MOD-label []
-synonym: "Methyl" RELATED PSI-MS-label []
-synonym: "Methylation" RELATED Unimod-description []
-synonym: "methyld" EXACT OMSSA-label []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 5 H 7 N 1 O 3" xsd:string
-property_value: MassAvg "129.12" xsd:float
-property_value: MassMono "129.042593" xsd:float
-property_value: Origin "D" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:34
-is_a: MOD:00599
-is_a: MOD:00887
-
-[Term]
-id: MOD:01682
-name: monomethylated L-cysteine
-def: "A protein modification that effectively replaces one hydrogen atom of an L-cysteine residue with one methyl group." [OMSSA:73, Unimod:34#C]
-subset: PSI-MOD-slim
-synonym: "Me1Cys" EXACT PSI-MOD-label []
-synonym: "Methyl" RELATED PSI-MS-label []
-synonym: "Methylation" RELATED Unimod-description []
-synonym: "methylc" EXACT OMSSA-label []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 4 H 7 N 1 O 1 S 1" xsd:string
-property_value: MassAvg "117.17" xsd:float
-property_value: MassMono "117.024835" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:34
-is_a: MOD:00599
-is_a: MOD:00660
-
-[Term]
-id: MOD:01683
-name: monomethylated L-lysine
-def: "A protein modification that effectively replaces one hydrogen atom of an L-lysine residue with one methyl group." [OMSSA:0]
-subset: PSI-MOD-slim
-synonym: "Me1Lys" EXACT PSI-MOD-label []
-synonym: "Methyl" RELATED PSI-MS-label []
-synonym: "Methylation" RELATED Unimod-description []
-synonym: "methylk" EXACT OMSSA-label []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 7 H 15 N 2 O 2" xsd:string
-property_value: MassAvg "159.21" xsd:float
-property_value: MassMono "159.113353" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00599
-is_a: MOD:00663
-
-[Term]
-id: MOD:01684
-name: palmitoylated-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to a palmitoylated-L-cysteine, such as N-palmitoyl-L-cysteine or S-palmitoyl-L-cysteine." [OMSSA:92, Unimod:47]
-subset: PSI-MOD-slim
-synonym: "Palmitoyl" RELATED PSI-MS-label []
-synonym: "Palmitoylation" RELATED Unimod-description []
-synonym: "palmitoylationc" EXACT OMSSA-label []
-synonym: "PamCys" EXACT PSI-MOD-label []
-synonym: "Hexadecanoylated L-cysteine" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "238.41" xsd:float
-property_value: DiffFormula "C 16 H 30 N 0 O 1 S 0" xsd:string
-property_value: DiffMono "238.229666" xsd:float
-property_value: Formula "C 19 H 35 N 1 O 2 S 1" xsd:string
-property_value: MassAvg "341.55" xsd:float
-property_value: MassMono "341.238850" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:47
-is_a: MOD:00905
-
-[Term]
-id: MOD:01685
-name: alpha-amino palmitoylated residue
-def: "A protein modification that effectively replaces a residue alpha-amino group with a alpha-palmitoylamino group." [Unimod:47#N-term]
-subset: PSI-MOD-slim
-synonym: "N2PamRes" EXACT PSI-MOD-label []
-synonym: "Palmitoyl" RELATED PSI-MS-label []
-synonym: "Palmitoylation" RELATED Unimod-description []
-property_value: DiffAvg "238.41" xsd:float
-property_value: DiffFormula "C 16 H 30 N 0 O 1 S 0" xsd:string
-property_value: DiffMono "238.229666" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:47
-is_a: MOD:00651
-is_a: MOD:01696
-
-[Term]
-id: MOD:01686
-name: alpha-amino dimethylated residue
-def: "A protein modification that effectively replaces two alpha amino hydrogen atoms with two methyl group." [OMSSA:38, Unimod:36#N-term]
-comment: For alpha-amino acids, both N-alpha-monomethylation and complete N-alpha protonation and trimethylation have been observed, but incomplete dimethylation has not been reported as a natural process. For N-terminal proline residues, dimethylation can only be effectively accomplished with a protonated imino group, whereas this process accounts only for dimethylation and not protonation. See MOD:00889.
-synonym: "di-Methylation" RELATED Unimod-description []
-synonym: "Dimethyl" RELATED PSI-MS-label []
-synonym: "N2Me2Res" EXACT PSI-MOD-label []
-synonym: "ntermpepdimethyl" EXACT OMSSA-label []
-property_value: DiffAvg "28.05" xsd:float
-property_value: DiffFormula "C 2 H 4" xsd:string
-property_value: DiffMono "28.031300" xsd:float
-property_value: Origin "X" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:36
-is_a: MOD:00429
-is_a: MOD:01460
-
-[Term]
-id: MOD:01687
-name: alpha-amino trimethylated residue
-def: "A protein modification that effectively replaces an alpha-aminium group with a trimethylaminium group." [OMSSA:12, Unimod:37#N-term]
-comment: For amino acids residues, amine trimethylation can effectively only be accomplished with an aminium, protonated primary amino, group. This process accounts only for trimethylation and not protonation. The alternative N2Me3+Res process (MOD:01698) accounts for both protonation and trimethylation.
-subset: PSI-MOD-slim
-synonym: "N2Me3Res" EXACT PSI-MOD-label []
-synonym: "ntermtrimethyl" EXACT OMSSA-label []
-synonym: "tri-Methylation" RELATED Unimod-description []
-synonym: "Trimethyl" RELATED PSI-MS-label []
-property_value: DiffAvg "42.08" xsd:float
-property_value: DiffFormula "C 3 H 6 N 0 O 0" xsd:string
-property_value: DiffMono "42.046402" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:37
-is_a: MOD:00430
-is_a: MOD:01460
-relationship: derives_from MOD:01700
-
-[Term]
-id: MOD:01688
-name: 3-hydroxy-L-asparagine
-def: "A protein modification that effectively converts an L-asparagine residue to one of the diastereomeric 3-hydroxy-L-asparagine residues." [OMSSA:61, Unimod:35#N]
-subset: PSI-MOD-slim
-synonym: "3HyAsn" EXACT PSI-MOD-label []
-synonym: "hydroxylationn" EXACT OMSSA-label []
-synonym: "monohydroxylated asparagine" EXACT PSI-MOD-alternate []
-synonym: "Oxidation" RELATED PSI-MS-label []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 4 H 6 N 2 O 3" xsd:string
-property_value: MassAvg "130.10" xsd:float
-property_value: MassMono "130.037842" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:35
-is_a: MOD:00425
-is_a: MOD:00903
-
-[Term]
-id: MOD:01689
-name: alpha-carboxyl methylated residue
-def: "A protein modification that effectively converts a carboxyl-terminal residue to an alpha-carboxyl (1-carboxyl) methyl ester." [OMSSA:18, OMSSA:68, Unimod:34#C-term]
-subset: PSI-MOD-slim
-synonym: "C1OMeRes" EXACT PSI-MOD-label []
-synonym: "ctermpepmeester" EXACT OMSSA-label []
-synonym: "ctermpepmethyl" EXACT OMSSA-label []
-synonym: "Methyl" RELATED PSI-MS-label []
-synonym: "Methyl" RELATED Unimod-alternate []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: Unimod:34
-is_a: MOD:00393
-
-[Term]
-id: MOD:01690
-name: N-[(12R)-12-hydroxymyristoyl]-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to N-[(12R)-12-hydroxymyristoyl]-L-cysteine." [RESID:AA0516]
-synonym: "2-[(12R)-12-hydroxytetradecanoyl]amino-3-sulfanylpropanoic acid" EXACT RESID-systematic []
-synonym: "LIPID N-[(12R)-12-hydroxymyristoyl]cysteine" EXACT UniProt-feature []
-synonym: "N-[(12R)-12-hydroxymyristoyl]-L-cysteine" EXACT RESID-name []
-synonym: "N-[(12R)-12-hydroxytetradecanoyl]cysteine" EXACT RESID-alternate []
-property_value: DiffAvg "226.36" xsd:float
-property_value: DiffFormula "C 14 H 26 N 0 O 2 S 0" xsd:string
-property_value: DiffMono "226.193280" xsd:float
-property_value: Formula "C 17 H 32 N 1 O 3 S 1" xsd:string
-property_value: MassAvg "330.51" xsd:float
-property_value: MassMono "330.210290" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0419
-is_a: MOD:00905
-is_a: MOD:01696
-
-[Term]
-id: MOD:01691
-name: N-(12-ketomyristoyl)-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to N-(12-ketomyristoyl)-L-cysteine." [PubMed:19053188, RESID:AA0517]
-synonym: "2-(12-oxotetradecanoyl)amino-3-sulfanylpropanoic acid" EXACT RESID-systematic []
-synonym: "LIPID N-(12-oxomyristoyl)cysteine" EXACT UniProt-feature []
-synonym: "N-(12-ketomyristoyl)-L-cysteine" EXACT RESID-name []
-synonym: "N-(12-oxotetradecanoyl)cysteine" EXACT RESID-alternate []
-property_value: DiffAvg "224.34" xsd:float
-property_value: DiffFormula "C 14 H 24 N 0 O 2 S 0" xsd:string
-property_value: DiffMono "224.177630" xsd:float
-property_value: Formula "C 17 H 30 N 1 O 3 S 1" xsd:string
-property_value: MassAvg "328.49" xsd:float
-property_value: MassMono "328.194640" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0420
-is_a: MOD:00905
-is_a: MOD:01696
-
-[Term]
-id: MOD:01692
-name: glutamyl semialdehyde (Glu)
-def: "A protein modification that effectively converts an L-glutamic acid residue to L-glutamyl semialdehyde." [PubMed:18688235, PubMed:743268]
-synonym: "Deoxy" RELATED PSI-MS-label []
-synonym: "gamma-glutamyl semialdehyde" EXACT PSI-MOD-alternate []
-synonym: "glutamyl 5-semialdehyde" EXACT PSI-MOD-alternate []
-synonym: "glutamyl aldehyde" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "-16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O -1" xsd:string
-property_value: DiffMono "-15.994915" xsd:float
-property_value: Formula "C 5 H 7 N 1 O 2" xsd:string
-property_value: MassAvg "113.12" xsd:float
-property_value: MassMono "113.047678" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00906
-is_a: MOD:01161
-is_a: MOD:01440
-
-[Term]
-id: MOD:01693
-name: alpha-amino pyridylacetylated residue
-def: "A protein modification that effectively replaces a residue alpha amino or imino hydrogen with a (pyrid-3-yl)acetyl group." [OMSSA:107, PubMed:9276974, Unimod:25#N-term]
-comment: Produced by reaction with N-[(pyrid-3-yl)acetyl]oxy-succinimide [JSG].
-synonym: "ntermpeppyridyl" EXACT OMSSA-label []
-synonym: "Pyridylacetyl" RELATED PSI-MS-label []
-synonym: "pyridylacetyl" RELATED Unimod-description []
-property_value: DiffAvg "119.12" xsd:float
-property_value: DiffFormula "C 7 H 5 N 1 O 1" xsd:string
-property_value: DiffMono "119.037114" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:25
-is_a: MOD:00418
-is_a: MOD:01696
-
-[Term]
-id: MOD:01694
-name: S-(coelenterazin-3a-yl)-L-cysteine
-def: "A protein modification that effectively results from forming an adduct between an L-cysteine residue and the bioluminescent compound didehydrocoelenterazine to form S-(coelenterazin-3a-yl)-L-cysteine." [ChEBI:2311, PubMed:18997450, RESID:AA0526]
-synonym: "(2R)-2-amino-3-([(4-hydroxyphenyl)(8-benzyl-3-oxo-6-[4-hydroxyphenyl]-3,7-dihydroimidazo[1,2-a]pyrazin-2-yl)methyl]sulfanyl)propanoic acid" EXACT RESID-systematic []
-synonym: "dehydrocoelenterazine cysteine adduct" EXACT RESID-alternate []
-synonym: "MOD_RES S-(coelenterazin-3a-yl)cysteine" EXACT UniProt-feature []
-synonym: "S-(coelenterazin-3a-yl)-L-cysteine" EXACT RESID-name []
-synonym: "symplectin chromophore" EXACT RESID-alternate []
-property_value: DiffAvg "421.46" xsd:float
-property_value: DiffFormula "C 26 H 19 N 3 O 3 S 0" xsd:string
-property_value: DiffMono "421.142641" xsd:float
-property_value: Formula "C 29 H 24 N 4 O 4 S 1" xsd:string
-property_value: MassAvg "524.60" xsd:float
-property_value: MassMono "524.151826" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0428
-is_a: MOD:00905
-
-[Term]
-id: MOD:01695
-name: alpha-amino 3-(carboxamidomethylthio)propanoylated residue
-def: "A protein modification that effectively replaces a residue alpha-amino- or alpha-imino-hydrogen with an 3-(carboxamidomethylthio)propanoyl group." [PubMed:15121203, Unimod:293#N-term]
-synonym: "3-(carbamidomethylthio)propanoyl" RELATED Unimod-description []
-synonym: "CAMthiopropanoyl" RELATED PSI-MS-label []
-property_value: DiffAvg "145.18" xsd:float
-property_value: DiffFormula "C 5 H 7 N 1 O 2 S 1" xsd:string
-property_value: DiffMono "145.019749" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:293
-is_a: MOD:00612
-is_a: MOD:01696
-
-[Term]
-id: MOD:01696
-name: alpha-amino acylated residue
-def: "A protein modification that effectively replaces a residue alpha-amino- or alpha-imino-hydrogen with an acyl group." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00670
-
-[Term]
-id: MOD:01697
-name: alpha-amino 4-(2-aminoethyl)benzenesulfonylated residue
-def: "A protein modification that effectively replaces a residue alpha-amino- or alpha-imino-hydrogen with an 4-(2-aminoethyl)benzenesulfonyl group." [DeltaMass:235, PubMed:8597590, Unimod:276#N-term]
-comment: See the comment for MOD:00596 [JSG].
-synonym: "AEBS" RELATED PSI-MS-label []
-synonym: "Aminoethylbenzenesulfonylation" RELATED Unimod-description []
-property_value: DiffAvg "183.23" xsd:float
-property_value: DiffFormula "C 8 H 9 N 1 O 2 S 1" xsd:string
-property_value: DiffMono "183.035400" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:276
-is_a: MOD:00596
-
-[Term]
-id: MOD:01698
-name: alpha-amino trimethylated protonated-residue
-def: "A protein modification that effectively replaces an amino group with a trimethylaminium group." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "N2Me3+Res" EXACT PSI-MOD-label []
-synonym: "tri-Methylation" RELATED Unimod-description []
-synonym: "Trimethyl" RELATED PSI-MS-label []
-property_value: DiffAvg "43.09" xsd:float
-property_value: DiffFormula "C 3 H 7 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "43.054227" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00711
-is_a: MOD:01460
-
-[Term]
-id: MOD:01699
-name: protonated residue
-def: "A protein modification that effectively adds a hydrogen cation, a proton, forming a cationic residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "H+NRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "1.01" xsd:float
-property_value: DiffFormula "C 0 H 1 N 0 O 0" xsd:string
-property_value: DiffMono "1.007276" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:01156
-
-[Term]
-id: MOD:01700
-name: alpha-amino protonated residue
-def: "A protein modification that effectively adds a proton to a residue alpha-amnino or alpha-imino group forming an alpha-aminium or alpha-iminium group, respectively." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "N2H+NRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "1.01" xsd:float
-property_value: DiffFormula "C 0 H 1 N 0 O 0" xsd:string
-property_value: DiffMono "1.007276" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:01699
-
-[Term]
-id: MOD:01701
-name: deprotonated residue
-def: "A protein modification that effectively removes a hydrogen cation, a proton, forming an anionic residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "H-NRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "-1.01" xsd:float
-property_value: DiffFormula "C 0 H -1 N 0 O 0" xsd:string
-property_value: DiffMono "-1.007276" xsd:float
-property_value: FormalCharge "1-" xsd:string
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:01156
-
-[Term]
-id: MOD:01702
-name: alpha-carboxyl deprotonated residue
-def: "A protein modification that effectively removes a proton from a residue 1-carboxyl group (referred to as the alpha-carboxyl), forming a carboxylate anion." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "C1H-NRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "-1.01" xsd:float
-property_value: DiffFormula "C 0 H -1 N 0 O 0" xsd:string
-property_value: DiffMono "-1.007276" xsd:float
-property_value: FormalCharge "1-" xsd:string
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-is_a: MOD:01701
-
-[Term]
-id: MOD:01703
-name: dehydrobutyrine
-def: "A protein modification that effectively converts a source amino acid residue to dehydrobutyrine." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "beta-elim-t" EXACT OMSSA-label []
-synonym: "Dehydrated" RELATED PSI-MS-label []
-synonym: "Dehydrated" RELATED Unimod-interim []
-synonym: "Dehydration" RELATED Unimod-description []
-synonym: "dehydro" EXACT OMSSA-label []
-synonym: "Dehydroamino butyric acid" EXACT DeltaMass-label []
-synonym: "dHAbu" EXACT PSI-MOD-label []
-synonym: "phospholosst" EXACT OMSSA-label []
-property_value: Formula "C 4 H 5 N 1 O 1" xsd:string
-property_value: MassAvg "83.09" xsd:float
-property_value: MassMono "83.037114" xsd:float
-property_value: Origin "X" xsd:string
-is_a: MOD:00859
-
-[Term]
-id: MOD:01704
-name: dehydrobutyrine (Met)
-def: "A protein modification that effectively converts an L-methionine residue to dehydrobutyrine, by neutral loss of methyl sulfide." [PubMed:18688235]
-comment: It is expected that this neutral loss will produce a mix of (E)- and (Z)-isomers [JSG].
-subset: PSI-MOD-slim
-synonym: "dHAbu(Met)" EXACT PSI-MOD-label []
-property_value: DiffAvg "-48.10" xsd:float
-property_value: DiffFormula "C -1 H -4 N 0 O 0 S -1" xsd:string
-property_value: DiffMono "-48.003371" xsd:float
-property_value: Formula "C 4 H 5 N 1 O 1" xsd:string
-property_value: MassAvg "83.09" xsd:float
-property_value: MassMono "83.037114" xsd:float
-property_value: Origin "M" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00913
-is_a: MOD:01703
-
-[Term]
-id: MOD:01705
-name: isotope tagged reagent acylated residue
-def: "A protein modification that effectively replaces a residue hydrogen with an isotope tagged reagent acyl group." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00649
-
-[Term]
-id: MOD:01706
-name: isotope tagged reagent N-acylated residue
-def: "A protein modification that effectively replaces a residue alpha-amino- or alpha-imino-hydrogen with an isotope tagged reagent acyl group." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00670
-
-[Term]
-id: MOD:01707
-name: isotope tagged reagent O-acylated residue
-def: "A protein modification that effectively replaces a residue hydroxyl group with an isotope tagged reagent acyloxy group." [PubMed:18688235]
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00671
-
-[Term]
-id: MOD:01708
-name: isotope tagged reagent alpha-amino acylated residue
-def: "A protein modification that effectively replaces a residue alpha-amino- or alpha-imino-hydrogen with an isotope tagged reagent acyl group." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:01696
-is_a: MOD:01705
-is_a: MOD:01706
-
-[Term]
-id: MOD:01709
-name: iTRAQ4plex reporter+balance reagent N-acylated residue
-def: "A protein modification that effectively replaces a residue amino- or imino-hydrogen with one of the Applied Biosystems iTRAQ4plex reagent reporter+balance groups." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01706
-
-[Term]
-id: MOD:01710
-name: iTRAQ8plex reporter+balance reagent N-acylated residue
-def: "A protein modification that effectively replaces a residue amino- or imino-hydrogen with one of the Applied Biosystems iTRAQ8plex reagent reporter+balance groups." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01706
-
-[Term]
-id: MOD:01711
-name: iTRAQ4plex reporter+balance reagent acylated N-terminal
-def: "A protein modification that effectively replaces a residue alpha-amino- or alpha-imino-hydrogen with one of the Applied Biosystems iTRAQ4plex reagent reporter+balance groups." [Unimod:214#N-term]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:214
-is_a: MOD:01708
-is_a: MOD:01709
-
-[Term]
-id: MOD:01712
-name: iTRAQ8plex reporter+balance reagent acylated N-terminal
-def: "A protein modification that effectively replaces a residue alpha-amino- or alpha-imino-hydrogen with one of the Applied Biosystems iTRAQ8plex reagent reporter+balance groups." [Unimod:214#N-term]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:214
-is_a: MOD:01708
-is_a: MOD:01710
-
-[Term]
-id: MOD:01713
-name: iTRAQ4plex reporter+balance reagent O-acylated residue
-def: "A protein modification that effectively replaces a residue hydroxyl with one of the Applied Biosystems iTRAQ4plex reagent reporter+balance acyloxy groups." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01707
-
-[Term]
-id: MOD:01714
-name: iTRAQ8plex reporter+balance reagent O-acylated residue
-def: "A protein modification that effectively replaces a residue hydroxyl with one of the Applied Biosystems iTRAQ8plex reagent reporter+balance acyloxy groups." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01707
-
-[Term]
-id: MOD:01715
-name: TMT6plex reporter+balance reagent acylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of a residue with a Proteome Sciences TMT6plex reporter+balance group." [Unimod:214]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:214
-is_a: MOD:01426
-is_a: MOD:01428
-is_a: MOD:01429
-is_a: MOD:01705
-
-[Term]
-id: MOD:01716
-name: TMT6plex reporter fragment
-def: "The protein modification reporter fragment produced by an Proteome Sciences TMT6plex-126 reagent acylated residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "2,6-dimethyl-1-methylidenepiperidinium" EXACT PSI-MOD-alternate []
-synonym: "cysTMT6plex reporter fragment" EXACT PSI-MOD-alternate []
-is_a: MOD:01520
-relationship: derives_from MOD:01715
-relationship: derives_from MOD:01821
-
-[Term]
-id: MOD:01717
-name: TMT6plex reporter+balance reagent N-acylated residue
-def: "A protein modification that effectively replaces a residue amino- or imino-hydrogen with a Proteome Sciences TMT6plex reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01706
-
-[Term]
-id: MOD:01718
-name: TMT6plex reporter+balance reagent acylated N-terminal
-def: "A protein modification that effectively replaces a residue alpha-amino- or alpha-imino-hydrogen with a Proteome Sciences TMT6plex reporter+balance group." [Unimod:214#N-term]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:214
-is_a: MOD:01708
-is_a: MOD:01717
-
-[Term]
-id: MOD:01719
-name: TMT6plex reporter+balance reagent O-acylated residue
-def: "A protein modification that effectively replaces a residue hydroxyl with one of the Proteome Sciences TMT6plex reagent reporter+balance acyloxy groups." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01707
-
-[Term]
-id: MOD:01720
-name: TMT6plex-126 reporter+balance reagent acylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of a residue with the Proteome Sciences TMT6plex-126 reporter+balance group." [Unimod:737]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:737
-is_a: MOD:01715
-
-[Term]
-id: MOD:01721
-name: TMT6plex-126 reporter+balance reagent acylated N-terminal
-def: "A protein modification that effectively replaces a hydrogen atom of a protein N-terminal with the Proteome Sciences TMT6plex-126 reporter+balance group." [Unimod:737#N-term]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:737
-is_a: MOD:01718
-is_a: MOD:01720
-
-[Term]
-id: MOD:01722
-name: TMT6plex-126 reporter+balance reagent N6-acylated lysine
-def: "A protein modification that effectively replaces the N6'-hydrogen atom of a lysine residue with the Proteome Sciences TMT6plex-126 reporter+balance group." [Unimod:737#K]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Formula "(12)C 14 (13)C 4 H 32 (14)N 3 (15)N 1 O 3" xsd:string
-property_value: MassAvg "357.26" xsd:float
-property_value: MassMono "357.257895" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:737
-is_a: MOD:01717
-is_a: MOD:01720
-is_a: MOD:01875
-
-[Term]
-id: MOD:01723
-name: TMT6plex-126 reporter+balance reagent O4'-acylated tyrosine
-def: "A protein modification that effectively replaces the O4'-hydrogen atom of a tyrosine residue with the Proteome Sciences TMT6plex-126 reporter+balance group." [Unimod:737#Y]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Formula "(12)C 17 (13)C 4 H 29 (14)N 2 (15)N 1 O 4" xsd:string
-property_value: MassAvg "392.23" xsd:float
-property_value: MassMono "392.226261" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:737
-is_a: MOD:00919
-is_a: MOD:01719
-is_a: MOD:01720
-
-[Term]
-id: MOD:01724
-name: TMT6plex-126 reporter+balance reagent N'-acylated histidine
-def: "A protein modification that effectively replaces an N'-hydrogen atom of a histidine residue with the Proteome Sciences TMT6plex-126 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Formula "(12)C 14 (13)C 4 H 27 (14)N 4 (15)N 1 O 3" xsd:string
-property_value: MassAvg "366.22" xsd:float
-property_value: MassMono "366.221844" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00909
-is_a: MOD:01717
-is_a: MOD:01720
-
-[Term]
-id: MOD:01725
-name: TMT6plex-126 reporter+balance reagent O3-acylated serine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a serine residue with the Proteome Sciences TMT6plex-126 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Formula "(12)C 11 (13)C 4 H 25 (14)N 2 (15)N 1 O 4" xsd:string
-property_value: MassAvg "316.19" xsd:float
-property_value: MassMono "316.194961" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02003
-is_a: MOD:01719
-is_a: MOD:01720
-
-[Term]
-id: MOD:01726
-name: TMT6plex-126 reporter+balance reagent O3-acylated threonine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a threonine residue with the Proteome Sciences TMT6plex-126 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Formula "(12)C 12 (13)C 4 H 27 (14)N 2 (15)N 1 O 4" xsd:string
-property_value: MassAvg "330.21" xsd:float
-property_value: MassMono "330.210611" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02004
-is_a: MOD:01719
-is_a: MOD:01720
-
-[Term]
-id: MOD:01727
-name: TMT6plex-126 reporter fragment
-def: "The protein modification reporter fragment produced by an Proteome Sciences TMT6plex-126 reagent acylated residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "2,6-dimethyl-1-methylidenepiperidinium" EXACT PSI-MOD-alternate []
-synonym: "cysTMT6plex-126 reporter fragment" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "(12)C 8 H 16 (14)N 1" xsd:string
-property_value: MassAvg "126.13" xsd:float
-property_value: MassMono "126.127726" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01716
-relationship: derives_from MOD:01720
-relationship: derives_from MOD:01822
-relationship: derives_from MOD:01823
-
-[Term]
-id: MOD:01728
-name: TMT6plex-127 reporter+balance reagent acylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of a residue with the Proteome Sciences TMT6plex-127 reporter+balance group." [Unimod:737]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:737
-is_a: MOD:01715
-
-[Term]
-id: MOD:01729
-name: TMT6plex-127 reporter+balance reagent acylated N-terminal
-def: "A protein modification that effectively replaces a hydrogen atom of a protein N-terminal with the Proteome Sciences TMT6plex-127 reporter+balance group." [Unimod:737#N-term]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:01718
-is_a: MOD:01728
-
-[Term]
-id: MOD:01730
-name: TMT6plex-127 reporter+balance reagent N6-acylated lysine
-def: "A protein modification that effectively replaces the N6'-hydrogen atom of a lysine residue with the Proteome Sciences TMT6plex-127 reporter+balance group." [Unimod:737#K]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Formula "(12)C 14 (13)C 4 H 32 (14)N 3 (15)N 1 O 3" xsd:string
-property_value: MassAvg "357.26" xsd:float
-property_value: MassMono "357.257895" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:737
-is_a: MOD:01717
-is_a: MOD:01728
-is_a: MOD:01875
-
-[Term]
-id: MOD:01731
-name: TMT6plex-127 reporter+balance reagent O4'-acylated tyrosine
-def: "A protein modification that effectively replaces the O4'-hydrogen atom of a tyrosine residue with the Proteome Sciences TMT6plex-127 reporter+balance group." [Unimod:737#Y]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Formula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: MassAvg "229.16" xsd:float
-property_value: MassMono "229.162932" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00919
-is_a: MOD:01719
-is_a: MOD:01728
-
-[Term]
-id: MOD:01732
-name: TMT6plex-127 reporter+balance reagent N'-acylated histidine
-def: "A protein modification that effectively replaces an N'-hydrogen atom of a histidine residue with the Proteome Sciences TMT6plex-127 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Formula "(12)C 14 (13)C 4 H 27 (14)N 4 (15)N 1 O 3" xsd:string
-property_value: MassAvg "366.22" xsd:float
-property_value: MassMono "366.221844" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00909
-is_a: MOD:01717
-is_a: MOD:01728
-
-[Term]
-id: MOD:01733
-name: TMT6plex-127 reporter+balance reagent O3-acylated serine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a serine residue with the Proteome Sciences TMT6plex-127 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Formula "(12)C 11 (13)C 4 H 25 (14)N 2 (15)N 1 O 4" xsd:string
-property_value: MassAvg "316.19" xsd:float
-property_value: MassMono "316.194961" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02003
-is_a: MOD:01719
-is_a: MOD:01728
-
-[Term]
-id: MOD:01734
-name: TMT6plex-127 reporter+balance reagent O3-acylated threonine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a threonine residue with the Proteome Sciences TMT6plex-127 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Formula "(12)C 12 (13)C 4 H 27 (14)N 2 (15)N 1 O 4" xsd:string
-property_value: MassAvg "330.21" xsd:float
-property_value: MassMono "330.210611" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02004
-is_a: MOD:01719
-is_a: MOD:01728
-
-[Term]
-id: MOD:01735
-name: TMT6plex-127 reporter fragment
-def: "The protein modification reporter fragment produced by an Proteome Sciences TMT6plex-127 reagent acylated residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "2,6-dimethyl-1-methylidenepiperidinium" EXACT PSI-MOD-alternate []
-synonym: "cysTMT6plex-127 reporter fragment" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "(12)C 7 (13)C 1 H 16 (14)N 1" xsd:string
-property_value: MassAvg "127.13" xsd:float
-property_value: MassMono "127.131081" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01716
-relationship: derives_from MOD:01728
-relationship: derives_from MOD:01824
-
-[Term]
-id: MOD:01736
-name: TMT6plex-128 reporter+balance reagent acylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of a residue with the Proteome Sciences TMT6plex-128 reporter+balance group." [Unimod:737]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:737
-is_a: MOD:01715
-
-[Term]
-id: MOD:01737
-name: TMT6plex-128 reporter+balance reagent acylated N-terminal
-def: "A protein modification that effectively replaces a hydrogen atom of a protein N-terminal with the Proteome Sciences TMT6plex-128 reporter+balance group." [Unimod:737#N-term]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:737
-is_a: MOD:01718
-is_a: MOD:01736
-
-[Term]
-id: MOD:01738
-name: TMT6plex-128 reporter+balance reagent N6-acylated lysine
-def: "A protein modification that effectively replaces the N6'-hydrogen atom of a lysine residue with the Proteome Sciences TMT6plex-128 reporter+balance group." [Unimod:737#K]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Formula "(12)C 14 (13)C 4 H 32 (14)N 3 (15)N 1 O 3" xsd:string
-property_value: MassAvg "357.26" xsd:float
-property_value: MassMono "357.257895" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:737
-is_a: MOD:01717
-is_a: MOD:01736
-is_a: MOD:01875
-
-[Term]
-id: MOD:01739
-name: TMT6plex-128 reporter+balance reagent O4'-acylated tyrosine
-def: "A protein modification that effectively replaces the O4'-hydrogen atom of a tyrosine residue with the Proteome Sciences TMT6plex-128 reporter+balance group." [Unimod:737#Y]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Formula "(12)C 17 (13)C 4 H 29 (14)N 2 (15)N 1 O 4" xsd:string
-property_value: MassAvg "392.23" xsd:float
-property_value: MassMono "392.226261" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:737
-is_a: MOD:00919
-is_a: MOD:01719
-is_a: MOD:01736
-
-[Term]
-id: MOD:01740
-name: TMT6plex-128 reporter+balance reagent N'-acylated histidine
-def: "A protein modification that effectively replaces an N'-hydrogen atom of a histidine residue with the Proteome Sciences TMT6plex-128 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Formula "(12)C 14 (13)C 4 H 27 (14)N 4 (15)N 1 O 3" xsd:string
-property_value: MassAvg "366.22" xsd:float
-property_value: MassMono "366.221844" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00909
-is_a: MOD:01717
-is_a: MOD:01736
-
-[Term]
-id: MOD:01741
-name: TMT6plex-128 reporter+balance reagent O3-acylated serine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a serine residue with the Proteome Sciences TMT6plex-128 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Formula "(12)C 11 (13)C 4 H 25 (14)N 2 (15)N 1 O 4" xsd:string
-property_value: MassAvg "316.19" xsd:float
-property_value: MassMono "316.194961" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02003
-is_a: MOD:01719
-is_a: MOD:01736
-
-[Term]
-id: MOD:01742
-name: TMT6plex-128 reporter+balance reagent O3-acylated threonine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a threonine residue with the Proteome Sciences TMT6plex-128 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Formula "(12)C 12 (13)C 4 H 27 (14)N 2 (15)N 1 O 4" xsd:string
-property_value: MassAvg "330.21" xsd:float
-property_value: MassMono "330.210611" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02004
-is_a: MOD:01719
-is_a: MOD:01736
-
-[Term]
-id: MOD:01743
-name: TMT6plex-128 reporter fragment
-def: "The protein modification reporter fragment produced by an Proteome Sciences TMT6plex-128 reagent acylated residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "2,6-dimethyl-1-methylidenepiperidinium" EXACT PSI-MOD-alternate []
-synonym: "cysTMT6plex-128 reporter fragment" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "(12)C 6 (13)C 2 H 16 (14)N 1" xsd:string
-property_value: MassAvg "128.13" xsd:float
-property_value: MassMono "128.134436" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01716
-relationship: derives_from MOD:01736
-relationship: derives_from MOD:01825
-
-[Term]
-id: MOD:01744
-name: TMT6plex-129 reporter+balance reagent acylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of a residue with the Proteome Sciences TMT6plex-129 reporter+balance group." [Unimod:737]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:737
-is_a: MOD:01715
-
-[Term]
-id: MOD:01745
-name: TMT6plex-129 reporter+balance reagent acylated N-terminal
-def: "A protein modification that effectively replaces a hydrogen atom of a protein N-terminal with the Proteome Sciences TMT6plex-129 reporter+balance group." [Unimod:737#N-term]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:737
-is_a: MOD:01718
-is_a: MOD:01744
-
-[Term]
-id: MOD:01746
-name: TMT6plex-129 reporter+balance reagent N6-acylated lysine
-def: "A protein modification that effectively replaces the N6'-hydrogen atom of a lysine residue with the Proteome Sciences TMT6plex-129 reporter+balance group." [Unimod:737#K]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Formula "(12)C 14 (13)C 4 H 32 (14)N 3 (15)N 1 O 3" xsd:string
-property_value: MassAvg "357.26" xsd:float
-property_value: MassMono "357.257895" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:737
-is_a: MOD:01717
-is_a: MOD:01744
-is_a: MOD:01875
-
-[Term]
-id: MOD:01747
-name: TMT6plex-129 reporter+balance reagent O4'-acylated tyrosine
-def: "A protein modification that effectively replaces the O4'-hydrogen atom of a tyrosine residue with the Proteome Sciences TMT6plex-129 reporter+balance group." [Unimod:737#Y]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Formula "(12)C 17 (13)C 4 H 29 (14)N 2 (15)N 1 O 4" xsd:string
-property_value: MassAvg "392.23" xsd:float
-property_value: MassMono "392.226261" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:737
-is_a: MOD:00919
-is_a: MOD:01719
-is_a: MOD:01744
-
-[Term]
-id: MOD:01748
-name: TMT6plex-129 reporter+balance reagent N'-acylated histidine
-def: "A protein modification that effectively replaces an N'-hydrogen atom of a histidine residue with the Proteome Sciences TMT6plex-129 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Formula "(12)C 14 (13)C 4 H 27 (14)N 4 (15)N 1 O 3" xsd:string
-property_value: MassAvg "366.22" xsd:float
-property_value: MassMono "366.221844" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00909
-is_a: MOD:01717
-is_a: MOD:01744
-
-[Term]
-id: MOD:01749
-name: TMT6plex-129 reporter+balance reagent O3-acylated serine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a serine residue with the Proteome Sciences TMT6plex-129 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Formula "(12)C 11 (13)C 4 H 25 (14)N 2 (15)N 1 O 4" xsd:string
-property_value: MassAvg "316.19" xsd:float
-property_value: MassMono "316.194961" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02003
-is_a: MOD:01719
-is_a: MOD:01744
-
-[Term]
-id: MOD:01750
-name: TMT6plex-129 reporter+balance reagent O3-acylated threonine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a threonine residue with the Proteome Sciences TMT6plex-129 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Formula "(12)C 12 (13)C 4 H 27 (14)N 2 (15)N 1 O 4" xsd:string
-property_value: MassAvg "330.21" xsd:float
-property_value: MassMono "330.210611" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02004
-is_a: MOD:01719
-is_a: MOD:01744
-
-[Term]
-id: MOD:01751
-name: TMT6plex-129 reporter fragment
-def: "The protein modification reporter fragment produced by an Proteome Sciences TMT6plex-129 reagent acylated residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "2,6-dimethyl-1-methylidenepiperidinium" EXACT PSI-MOD-alternate []
-synonym: "cysTMT6plex-129 reporter fragment" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "(12)C 5 (13)C 3 H 16 (14)N 1" xsd:string
-property_value: MassAvg "129.14" xsd:float
-property_value: MassMono "129.137790" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01716
-relationship: derives_from MOD:01744
-relationship: derives_from MOD:01826
-
-[Term]
-id: MOD:01752
-name: TMT6plex-130 reporter+balance reagent acylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of a residue with the Proteome Sciences TMT6plex-130 reporter+balance group." [Unimod:737]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:737
-is_a: MOD:01715
-relationship: derives_from MOD:01827
-
-[Term]
-id: MOD:01753
-name: TMT6plex-130 reporter+balance reagent acylated N-terminal
-def: "A protein modification that effectively replaces a hydrogen atom of a protein N-terminal with the Proteome Sciences TMT6plex-130 reporter+balance group." [Unimod:737#N-term]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:737
-is_a: MOD:01718
-is_a: MOD:01752
-
-[Term]
-id: MOD:01754
-name: TMT6plex-130 reporter+balance reagent N6-acylated lysine
-def: "A protein modification that effectively replaces the N6'-hydrogen atom of a lysine residue with the Proteome Sciences TMT6plex-130 reporter+balance group." [Unimod:737#K]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Formula "(12)C 14 (13)C 4 H 32 (14)N 3 (15)N 1 O 3" xsd:string
-property_value: MassAvg "357.26" xsd:float
-property_value: MassMono "357.257895" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:737
-is_a: MOD:01717
-is_a: MOD:01752
-is_a: MOD:01875
-
-[Term]
-id: MOD:01755
-name: TMT6plex-130 reporter+balance reagent O4'-acylated tyrosine
-def: "A protein modification that effectively replaces the O4'-hydrogen atom of a tyrosine residue with the Proteome Sciences TMT6plex-130 reporter+balance group." [Unimod:737#Y]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Formula "(12)C 17 (13)C 4 H 29 (14)N 2 (15)N 1 O 4" xsd:string
-property_value: MassAvg "392.23" xsd:float
-property_value: MassMono "392.226261" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:737
-is_a: MOD:00919
-is_a: MOD:01719
-is_a: MOD:01752
-
-[Term]
-id: MOD:01756
-name: TMT6plex-130 reporter+balance reagent N'-acylated histidine
-def: "A protein modification that effectively replaces an N'-hydrogen atom of a histidine residue with the Proteome Sciences TMT6plex-130 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Formula "(12)C 14 (13)C 4 H 27 (14)N 4 (15)N 1 O 3" xsd:string
-property_value: MassAvg "366.22" xsd:float
-property_value: MassMono "366.221844" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00909
-is_a: MOD:01717
-is_a: MOD:01752
-
-[Term]
-id: MOD:01757
-name: TMT6plex-130 reporter+balance reagent O3-acylated serine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a serine residue with the Proteome Sciences TMT6plex-130 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Formula "(12)C 11 (13)C 4 H 25 (14)N 2 (15)N 1 O 4" xsd:string
-property_value: MassAvg "316.19" xsd:float
-property_value: MassMono "316.194961" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02003
-is_a: MOD:01719
-is_a: MOD:01752
-
-[Term]
-id: MOD:01758
-name: TMT6plex-130 reporter+balance reagent O3-acylated threonine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a threonine residue with the Proteome Sciences TMT6plex-130 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Formula "(12)C 12 (13)C 4 H 27 (14)N 2 (15)N 1 O 4" xsd:string
-property_value: MassAvg "330.21" xsd:float
-property_value: MassMono "330.210611" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02004
-is_a: MOD:01719
-is_a: MOD:01752
-
-[Term]
-id: MOD:01759
-name: TMT6plex-130 reporter fragment
-def: "The protein modification reporter fragment produced by an Proteome Sciences TMT6plex-130 reagent acylated residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "2,6-dimethyl-1-methylidenepiperidinium" EXACT PSI-MOD-alternate []
-synonym: "cysTMT6plex-130 reporter fragment" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "(12)C 4 (13)C 4 H 16 (14)N 1" xsd:string
-property_value: MassAvg "130.14" xsd:float
-property_value: MassMono "130.141145" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01716
-relationship: derives_from MOD:01752
-
-[Term]
-id: MOD:01760
-name: TMT6plex-131 reporter+balance reagent acylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of a residue with the Proteome Sciences TMT6plex-131 reporter+balance group." [Unimod:737]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "cysTMT6plex-131 reporter fragment" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:737
-is_a: MOD:01715
-relationship: derives_from MOD:01828
-
-[Term]
-id: MOD:01761
-name: TMT6plex-131 reporter+balance reagent acylated N-terminal
-def: "A protein modification that effectively replaces a hydrogen atom of a protein N-terminal with the Proteome Sciences TMT6plex-131 reporter+balance group." [Unimod:737#N-term]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:737
-is_a: MOD:01718
-is_a: MOD:01760
-
-[Term]
-id: MOD:01762
-name: TMT6plex-131 reporter+balance reagent N6-acylated lysine
-def: "A protein modification that effectively replaces the N6'-hydrogen atom of a lysine residue with the Proteome Sciences TMT6plex-131 reporter+balance group." [Unimod:737#K]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Formula "(12)C 14 (13)C 4 H 32 (14)N 3 (15)N 1 O 3" xsd:string
-property_value: MassAvg "357.26" xsd:float
-property_value: MassMono "357.257895" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:737
-is_a: MOD:01717
-is_a: MOD:01760
-is_a: MOD:01875
-
-[Term]
-id: MOD:01763
-name: TMT6plex-131 reporter+balance reagent O4'-acylated tyrosine
-def: "A protein modification that effectively replaces the O4'-hydrogen atom of a tyrosine residue with the Proteome Sciences TMT6plex-131 reporter+balance group." [Unimod:737#Y]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Formula "(12)C 17 (13)C 4 H 29 (14)N 2 (15)N 1 O 4" xsd:string
-property_value: MassAvg "392.23" xsd:float
-property_value: MassMono "392.226261" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:737
-is_a: MOD:00919
-is_a: MOD:01719
-is_a: MOD:01760
-
-[Term]
-id: MOD:01764
-name: TMT6plex-131 reporter+balance reagent N'-acylated histidine
-def: "A protein modification that effectively replaces an N'-hydrogen atom of a histidine residue with the Proteome Sciences TMT6plex-131 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Formula "(12)C 14 (13)C 4 H 27 (14)N 4 (15)N 1 O 3" xsd:string
-property_value: MassAvg "366.22" xsd:float
-property_value: MassMono "366.221844" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00909
-is_a: MOD:01717
-is_a: MOD:01760
-
-[Term]
-id: MOD:01765
-name: TMT6plex-131 reporter+balance reagent O3-acylated serine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a serine residue with the Proteome Sciences TMT6plex-131 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Formula "(12)C 11 (13)C 4 H 25 (14)N 2 (15)N 1 O 4" xsd:string
-property_value: MassAvg "316.19" xsd:float
-property_value: MassMono "316.194961" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02003
-is_a: MOD:01719
-is_a: MOD:01760
-
-[Term]
-id: MOD:01766
-name: TMT6plex-131 reporter+balance reagent O3-acylated threonine
-def: "A protein modification that effectively replaces an O3-hydrogen atom of a threonine residue with the Proteome Sciences TMT6plex-131 reporter+balance group." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: DiffAvg "229.16" xsd:float
-property_value: DiffFormula "(12)C 8 (13)C 4 H 20 (14)N 1 (15)N 1 O 2" xsd:string
-property_value: DiffMono "229.162932" xsd:float
-property_value: Formula "(12)C 12 (13)C 4 H 27 (14)N 2 (15)N 1 O 4" xsd:string
-property_value: MassAvg "330.21" xsd:float
-property_value: MassMono "330.210611" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02004
-is_a: MOD:01719
-is_a: MOD:01760
-
-[Term]
-id: MOD:01767
-name: TMT6plex-131 reporter fragment
-def: "The protein modification reporter fragment produced by an Proteome Sciences TMT6plex-131 reagent acylated residue." [PubMed:18688235]
-synonym: "2,6-dimethyl-1-methylidenepiperidinium" EXACT PSI-MOD-alternate []
-synonym: "Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "TMT6plex" RELATED Unimod-alternate []
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "(12)C 4 (13)C 4 H 16 (15)N 1" xsd:string
-property_value: MassAvg "131.14" xsd:float
-property_value: MassMono "131.138180" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01716
-relationship: derives_from MOD:01760
-
-[Term]
-id: MOD:01768
-name: O-palmitoleylated residue
-def: "A protein modification that effectively replaces a residue hydroxyl group with a palmitoleyloxy group." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: DiffAvg "236.40" xsd:float
-property_value: DiffFormula "C 16 H 28 N 0 O 1" xsd:string
-property_value: DiffMono "236.214016" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00671
-is_a: MOD:01423
-
-[Term]
-id: MOD:01769
-name: O-palmitoleyl-L-threonine
-def: "A protein modification that effectively converts an L-threonine residue to O-palmitoleyl-L-threonine." [OMSSA:188, PubMed:6642431, PubMed:8413602, RESID:AA0079#var, Unimod:431#T]
-subset: PSI-MOD-slim
-synonym: "(2S,3R)-2-amino-3-((Z)-9-hexadecenoyloxy)butanoic acid" EXACT PSI-MOD-alternate []
-synonym: "L-threonine cis-9-hexadecenoate ester" EXACT PSI-MOD-alternate []
-synonym: "mod188" EXACT OMSSA-label []
-synonym: "O-palmitoleylated L-threonine" EXACT PSI-MOD-alternate []
-synonym: "O3-palmitoleyl-threonine" EXACT PSI-MOD-alternate []
-synonym: "Palmitoleyl" RELATED PSI-MS-label []
-synonym: "palmitoleyl" RELATED Unimod-description []
-property_value: DiffAvg "236.40" xsd:float
-property_value: DiffFormula "C 16 H 28 N 0 O 1" xsd:string
-property_value: DiffMono "236.214016" xsd:float
-property_value: Formula "C 20 H 35 N 1 O 3" xsd:string
-property_value: MassAvg "337.50" xsd:float
-property_value: MassMono "337.261694" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:431
-is_a: MOD:02004
-is_a: MOD:01768
-
-[Term]
-id: MOD:01770
-name: O-palmitoyl-L-threonine amide
-def: "A protein modification that effectively converts an L-threonine residue to O-palmitoyl-L-threonine amide." [PubMed:8413602, RESID:AA0079#var, RESID:AA0097#var]
-synonym: "(2S,3R)-2-amino-3-(hexadecanoyloxy)butanamide" EXACT PSI-MOD-alternate []
-synonym: "OPamThrN" EXACT PSI-MOD-label []
-property_value: DiffAvg "254.44" xsd:float
-property_value: DiffFormula "C 16 H 32 N 1 O 1" xsd:string
-property_value: DiffMono "254.248390" xsd:float
-property_value: Formula "C 20 H 39 N 2 O 3" xsd:string
-property_value: MassAvg "355.54" xsd:float
-property_value: MassMono "355.296068" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-is_a: MOD:02004
-relationship: has_functional_parent MOD:00088
-relationship: has_functional_parent MOD:00106
-
-[Term]
-id: MOD:01771
-name: farnesyl reporter fragment
-def: "The farnesyl cation protein modification reporter fragment produced by fragmentation of some farnesyl modified residues." [PubMed:15609361, PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-ylium" EXACT PSI-MOD-alternate []
-synonym: "Farn+" EXACT PSI-MOD-label []
-synonym: "farnesyl cation" EXACT PSI-MOD-alternate []
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 15 H 25" xsd:string
-property_value: MassAvg "205.36" xsd:float
-property_value: MassMono "205.195077" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:01520
-relationship: derives_from MOD:00437
-
-[Term]
-id: MOD:01772
-name: palmityl reporter fragment
-def: "The palmityl cation protein modification reporter fragment produced by fragmentation of some palmitoyl modified residues." [PubMed:18688235, PubMed:8413602]
-subset: PSI-MOD-slim
-synonym: "palmityl cation" RELATED PSI-MS-label []
-synonym: "Pam+" EXACT PSI-MOD-label []
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 16 H 31 O 1" xsd:string
-property_value: MassAvg "239.42" xsd:float
-property_value: MassMono "239.236942" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:01520
-relationship: derives_from MOD:00440
-
-[Term]
-id: MOD:01773
-name: N6,N6,N6-trimethyl-L-lysine with neutral loss of trimethylamine
-def: "Covalent modification of a trimethyllysine residue with secondary loss of a neutral trimethylamine molecular fragment." [PubMed:17205979, PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "dMe3N6Me3+Lys" EXACT PSI-MOD-label []
-property_value: DiffAvg "-59.11" xsd:float
-property_value: DiffFormula "C -3 H -9 N -1 O 0" xsd:string
-property_value: DiffMono "-59.074048" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 6 H 10 N 1 O 1" xsd:string
-property_value: MassAvg "112.15" xsd:float
-property_value: MassMono "112.075690" xsd:float
-property_value: Origin "MOD:00083" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00431
-is_a: MOD:00912
-relationship: derives_from MOD:00083
-
-[Term]
-id: MOD:01774
-name: N6-octanoyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-octanoyl-L-lysine." [PubMed:12591875, PubMed:2215217, RESID:AA0527]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-6-(octanoylamino)hexanoic acid" EXACT RESID-systematic []
-synonym: "epsilon-octanoyllysine" EXACT RESID-alternate []
-synonym: "N(zeta)-octanoyllysine" EXACT RESID-alternate []
-synonym: "N6-(1-oxooctyl)-L-lysine" EXACT RESID-alternate []
-synonym: "N6-octanoyl-L-lysine" EXACT RESID-name []
-property_value: DiffAvg "126.20" xsd:float
-property_value: DiffFormula "C 8 H 14 N 0 O 1" xsd:string
-property_value: DiffMono "126.104465" xsd:float
-property_value: Formula "C 14 H 26 N 2 O 2" xsd:string
-property_value: MassAvg "254.37" xsd:float
-property_value: MassMono "254.199428" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00666
-is_a: MOD:01875
-
-[Term]
-id: MOD:01775
-name: 5-glutamyl serotonin
-def: "A protein modification that effectively converts an L-glutamine residue to 5-glutamyl serotonin." [PubMed:11805836, PubMed:14697203, RESID:AA0528]
-synonym: "(2S)-2-amino-5-([2-(5-hydroxy-1H-indol-3-yl)ethyl]amino)-5-oxopentanoic acid" EXACT RESID-systematic []
-synonym: "5-glutamyl serotonin" EXACT RESID-name []
-synonym: "N2-(gamma-glutamyl)-5-hydoxytryptamine" EXACT RESID-alternate []
-synonym: "N5-[2-(5-hydroxy-3-indolyl)ethyl]glutamine" EXACT RESID-alternate []
-property_value: DiffAvg "159.19" xsd:float
-property_value: DiffFormula "C 10 H 9 N 1 O 1" xsd:string
-property_value: DiffMono "159.068414" xsd:float
-property_value: Formula "C 15 H 17 N 3 O 3" xsd:string
-property_value: MassAvg "287.32" xsd:float
-property_value: MassMono "287.126991" xsd:float
-property_value: Origin "Q" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00907
-
-[Term]
-id: MOD:01776
-name: S-methylthiocarbonylaminoethylcysteine (Cys)
-def: "A protein modification that effectively converts an L-cysteine residue to S-methylthiocarbonylaminoethylcysteine." [PubMed:18688235, PubMed:20608637]
-comment: This modified residue is a chemical analog of N6-acetyl-L-lysine produced from L-cysteine by methylthiocarbonylaziridine (MTCA, S-methyl aziridine-1-carbothioate).
-synonym: "(2R)-2-amino-3-([2-([(methylsulfanyl)carbonyl]amino)ethyl]sulfanyl)propanoic acid" EXACT PSI-MOD-alternate []
-synonym: "L-cysteine N-(methylthiocarbonyl)aziridine adduct" EXACT PSI-MOD-alternate []
-synonym: "MTCTK" EXACT PSI-MOD-alternate []
-synonym: "N6-methylthiocarbonyl-4-thialysine" EXACT PSI-MOD-alternate []
-synonym: "S-[2-([(methylthio)carbonyl]amino)ethyl]-L-cysteine" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "117.17" xsd:float
-property_value: DiffFormula "C 4 H 7 N 1 O 1 S 1" xsd:string
-property_value: DiffMono "117.024835" xsd:float
-property_value: Formula "C 7 H 12 N 2 O 2 S 2" xsd:string
-property_value: MassAvg "220.31" xsd:float
-property_value: MassMono "220.034020" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-is_a: MOD:00905
-
-[Term]
-id: MOD:01777
-name: S-(glycyl)-L-cysteine (Gly)
-def: "A protein modification that effectively converts a C-terminal glycine residue to S-(glycyl)-L-cysteine by forming a thioester bond with a free L-cysteine." [ChEBI:22050, PubMed:17726030, PubMed:18359941, PubMed:18771296, PubMed:18799456, PubMed:18842002, PubMed:3306404, RESID:AA0206]
-comment: This is not the cross-linking of two peptides, but the modification of a C-terminal glycine by formation of an thioester bond with a free cysteine. For the cross-linking of two peptide see MOD:00211 [JSG].
-synonym: "(2R)-2-amino-3-[(aminoacetyl)sulfanyl]propanoic acid" EXACT RESID-systematic []
-synonym: "1-(cystein-S-yl)-glycinate" EXACT RESID-alternate []
-synonym: "glycine cysteine thioester" EXACT RESID-alternate []
-synonym: "MOD_RES CysO-cysteine adduct" EXACT UniProt-feature []
-synonym: "S-(2-amino-1-oxoethyl)cysteine" EXACT RESID-alternate []
-synonym: "S-(glycyl)-L-cysteine" EXACT RESID-name []
-property_value: DiffAvg "103.14" xsd:float
-property_value: DiffFormula "C 3 H 5 N 1 O 1 S 1" xsd:string
-property_value: DiffMono "103.009185" xsd:float
-property_value: Formula "C 5 H 9 N 2 O 3 S 1" xsd:string
-property_value: MassAvg "177.20" xsd:float
-property_value: MassMono "177.033388" xsd:float
-property_value: Origin "G" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-is_a: MOD:00908
-
-[Term]
-id: MOD:01778
-name: N-(glycyl)-L-cysteine
-def: "A protein modification that effectively converts a C-terminal glycine residue to N-(glycyl)-L-cysteine by forming a peptide bond with a free L-cysteine." [PubMed:18771296, PubMed:18799456, PubMed:18842002, RESID:AA0529]
-synonym: "(2R)-2-[(aminoacetyl)amino]-3-sulfanylpropanoic acid" EXACT RESID-systematic []
-synonym: "MOD_RES CysO-cysteine adduct" EXACT UniProt-feature []
-synonym: "N-(2-amino-1-oxoethyl)cysteine" EXACT RESID-alternate []
-synonym: "N-(glycyl)-L-cysteine" EXACT RESID-name []
-property_value: DiffAvg "103.14" xsd:float
-property_value: DiffFormula "C 3 H 5 N 1 O 1 S 1" xsd:string
-property_value: DiffMono "103.009185" xsd:float
-property_value: Formula "C 5 H 9 N 2 O 3 S 1" xsd:string
-property_value: MassAvg "177.20" xsd:float
-property_value: MassMono "177.033388" xsd:float
-property_value: Origin "G" xsd:string
-property_value: Source "hypothetical" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0433
-is_a: MOD:00908
-
-[Term]
-id: MOD:01779
-name: N6-(L-lysyl)-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-(L-lysyl)-L-lysine by formation of an isopeptide bond between the carboxyl group of a free lysine and the N6-amino group of the peptidyl L-lysine." [PubMed:18201202, PubMed:20729861, RESID:AA0530]
-comment: This is not the cross-linking of two peptides, but the modification of a peptidyl lysine by formation of an isopeptide bond with a free lysine [JSG].
-synonym: "(2S)-2-amino-6-([(2S)-2,6-diaminohexanoyl]amino)hexanoic acid" EXACT RESID-systematic []
-synonym: "N6-(alpha-lysyl)-lysine" EXACT RESID-alternate []
-synonym: "N6-(L-lysyl)-L-lysine" EXACT RESID-name []
-property_value: DiffAvg "128.18" xsd:float
-property_value: DiffFormula "C 6 H 12 N 2 O 1" xsd:string
-property_value: DiffMono "128.094963" xsd:float
-property_value: Formula "C 12 H 24 N 4 O 2" xsd:string
-property_value: MassAvg "256.35" xsd:float
-property_value: MassMono "256.189926" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:01875
-
-[Term]
-id: MOD:01780
-name: N6-(beta-lysyl)-L-5-hydroxylysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-(beta-lysyl)-L-5-hydroxylysine by formation of an isopeptide bond between the carboxyl group of a free beta-lysine and the N6-amino group of a peptidyl L-lysine." [PubMed:18201202, PubMed:20729861, RESID:AA0531]
-synonym: "(2S)-2-amino-6-([(3R)-3,6-diaminohexanoyl]amino)-5-hydroxyhexanoic acid" EXACT RESID-systematic []
-synonym: "5-hydroxy-N6-(beta-lysyl)-L-lysine" EXACT RESID-name []
-synonym: "5-hydroxy-N6-[(3R)-beta-lysyl]lysine" EXACT RESID-alternate []
-synonym: "EF-P lysine derivative" EXACT RESID-alternate []
-synonym: "lysyl spermidine derivative [misidentification]" EXACT RESID-alternate []
-synonym: "MOD_RES N6-(3,6-diaminohexanoyl)-5-hydroxylysine" EXACT UniProt-feature []
-synonym: "N6-[(3R)-3,6-diaminohexanoyl]-L-5-hydroxylysine" EXACT RESID-alternate []
-property_value: DiffAvg "144.17" xsd:float
-property_value: DiffFormula "C 6 H 12 N 2 O 2" xsd:string
-property_value: DiffMono "144.089878" xsd:float
-property_value: Formula "C 12 H 24 N 4 O 3" xsd:string
-property_value: MassAvg "272.35" xsd:float
-property_value: MassMono "272.184841" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: uniprot.ptm:PTM-0474
-relationship: derives_from MOD:00037
-is_a: MOD:01875
-
-[Term]
-id: MOD:01781
-name: N6-butanoyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-butanoyl-L-lysine." [PubMed:17267393, PubMed:20715035, RESID:AA0532, Unimod:1289]
-comment: The binding of histone peptides with butanoylated lysine to nuclear bromodomain proteins is non-specific and weaker than binding to the corresponding acetylated lysine peptides [JSG].
-synonym: "(2S)-2-amino-6-(butanoylamino)hexanoic acid" EXACT RESID-systematic []
-synonym: "(2S)-2-azanyl-6-(butanoylamino)hexanoic acid" EXACT RESID-alternate []
-synonym: "2-amino-6-butyrylaminocaproic acid" EXACT RESID-alternate []
-synonym: "epsilon-butanoyl-L-lysine" EXACT RESID-alternate []
-synonym: "epsilon-butyryl-L-lysine" EXACT RESID-alternate []
-synonym: "N(zeta)-butanoyllysine" EXACT RESID-alternate []
-synonym: "N6-(1-oxobutyl)-L-lysine" EXACT RESID-alternate []
-synonym: "N6-butanoyl-L-lysine" EXACT RESID-name []
-synonym: "N6-butyryllysine" EXACT RESID-alternate []
-synonym: "MOD_RES N6-butyryllysine" EXACT UniProt-feature []
-property_value: DiffAvg "70.09" xsd:float
-property_value: DiffFormula "C 4 H 6 N 0 O 1" xsd:string
-property_value: DiffMono "70.041865" xsd:float
-property_value: Formula "C 10 H 18 N 2 O 2" xsd:string
-property_value: MassAvg "198.27" xsd:float
-property_value: MassMono "198.136828" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: Unimod:1289
-xref: uniprot.ptm:PTM-0637
-is_a: MOD:01875
-is_a: MOD:01997
-
-[Term]
-id: MOD:01782
-name: N-methyl-L-serine
-def: "A protein modification that effectively converts an L-serine residue to N-methyl-L-serine." [PubMed:20668449, RESID:AA0533]
-subset: PSI-MOD-slim
-synonym: "(2S)-3-hydroxy-2-(methylamino)propanoic acid" EXACT RESID-systematic []
-synonym: "MOD_RES N-methylserine" EXACT UniProt-feature []
-synonym: "N-methyl-L-serine" EXACT RESID-name []
-synonym: "N-methylserine" EXACT RESID-alternate []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 4 H 7 N 1 O 2" xsd:string
-property_value: MassAvg "101.10" xsd:float
-property_value: MassMono "101.047678" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0432
-is_a: MOD:01680
-is_a: MOD:01800
-
-[Term]
-id: MOD:01783
-name: N,N-dimethyl-L-serine
-def: "A protein modification that effectively converts an L-serine residue to N,N-dimethyl-L-serine." [PubMed:20668449, RESID:AA0534]
-synonym: "(2S)-2-(dimethylamino)propanoic acid" EXACT RESID-systematic []
-synonym: "MOD_RES N,N-dimethylserine" EXACT UniProt-feature []
-synonym: "N,N-dimethyl-L-serine" EXACT RESID-name []
-synonym: "N,N-dimethylserine" EXACT RESID-alternate []
-property_value: DiffAvg "28.05" xsd:float
-property_value: DiffFormula "C 2 H 4 N 0 O 0" xsd:string
-property_value: DiffMono "28.031300" xsd:float
-property_value: Formula "C 5 H 10 N 1 O 2" xsd:string
-property_value: MassAvg "116.14" xsd:float
-property_value: MassMono "116.071154" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0431
-is_a: MOD:01686
-is_a: MOD:01800
-
-[Term]
-id: MOD:01784
-name: N,N,N-trimethyl-L-serine
-def: "A protein modification that effectively converts an L-serine residue to N,N,N-trimethyl-L-serine." [PubMed:20668449, PubMed:3979397, RESID:AA0535]
-subset: PSI-MOD-slim
-synonym: "(1S)-1-carboxy-2-hydroxy-N,N,N-trimethylethanaminium" EXACT RESID-systematic []
-synonym: "(1S)-1-carboxy-2-hydroxy-N,N,N-trimethylethanazanium" EXACT RESID-alternate []
-synonym: "(2S)-2-trimethylammonio-3-hydroxypropanoic acid" EXACT RESID-alternate []
-synonym: "MOD_RES N,N,N-trimethylserine" EXACT UniProt-feature []
-synonym: "N,N,N-trimethyl-L-serine" EXACT RESID-name []
-synonym: "N,N,N-trimethylserine cation" EXACT RESID-alternate []
-synonym: "N,N,N-trimethylserinium" EXACT RESID-alternate []
-property_value: DiffAvg "43.09" xsd:float
-property_value: DiffFormula "C 3 H 7 N 0 O 0" xsd:string
-property_value: DiffMono "43.054227" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 6 H 13 N 1 O 2" xsd:string
-property_value: MassAvg "131.17" xsd:float
-property_value: MassMono "131.094080" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0430
-is_a: MOD:01698
-is_a: MOD:01800
-
-[Term]
-id: MOD:01785
-name: O-(L-isoglutamyl)-L-threonine (active site intermediate)
-def: "A protein modification that effectively converts an L-threonine residue to O-(L-isoglutamyl)-L-threonine, using free L-glutamine and releasing ammonia." [PubMed:8706862, RESID:AA0536#THR]
-comment: This is not an ester cross-link of peptides [JSG].
-synonym: "(2S)-2-amino-5-([(1S,2R)-1-amino-1-carboxypropan-2-yl]oxy)-5-oxopentanoic acid" EXACT RESID-systematic []
-synonym: "(2S,3R)-2-amino-3-([(4S)-4-amino-4-carboxybutanoyl]oxy)-propanoic acid" EXACT RESID-alternate []
-synonym: "5-(threon-O3-yl)glutamate" EXACT RESID-alternate []
-synonym: "O(beta)-(gamma-glutamyl)threonine" EXACT RESID-alternate []
-synonym: "O-(L-isoglutamyl)-L-threonine" EXACT RESID-name []
-synonym: "O3-(isoglutamyl)threonine" EXACT RESID-alternate []
-property_value: DiffAvg "129.12" xsd:float
-property_value: DiffFormula "C 5 H 7 N 1 O 3" xsd:string
-property_value: DiffMono "129.042593" xsd:float
-property_value: Formula "C 9 H 14 N 2 O 5" xsd:string
-property_value: MassAvg "230.22" xsd:float
-property_value: MassMono "230.090272" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "hypothetical" xsd:string
-is_a: MOD:00671
-is_a: MOD:01979
-
-[Term]
-id: MOD:01786
-name: 3'-nitro-L-tyrosine
-def: "A protein modification that effectively converts an L-tyrosine residue to 3'-nitro-L-tyrosine." [ChEBI:44454, PubMed:16944230, PubMed:5339594, RESID:AA0537]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-(4-hydroxy-3-nitrophenyl)propanoic acid" EXACT RESID-systematic []
-synonym: "3'-nitro-L-tyrosine" EXACT RESID-name []
-synonym: "3-nitro-L-tyrosine" EXACT RESID-alternate []
-synonym: "3-nitrotyrosine" EXACT RESID-alternate []
-synonym: "m-nitrotyrosine" EXACT RESID-alternate []
-synonym: "meta-nitrotyrosine" EXACT RESID-alternate []
-synonym: "MOD_RES 3'-Nitrotyrosine" EXACT UniProt-feature []
-property_value: DiffAvg "45.00" xsd:float
-property_value: DiffFormula "C 0 H -1 N 1 O 2" xsd:string
-property_value: DiffMono "44.985078" xsd:float
-property_value: Formula "C 9 H 8 N 2 O 4" xsd:string
-property_value: MassAvg "208.17" xsd:float
-property_value: MassMono "208.048407" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0434
-is_a: MOD:01352
-
-[Term]
-id: MOD:01787
-name: 5'-(L-tyros-5'-yl)amino-L-tyrosine
-def: "A protein modification that effectively cross-links two L-tyrosine residues through their 5' positions by amine nitrogen to form 5'-(L-tyros-5'-yl)amino-L-tyrosine." [PubMed:18781570, RESID:AA0459]
-comment: Cross-link 2.
-synonym: "(2S,2'S)-3,3'-[iminobis(4-hydroxybenzene-3,1-diyl)]bis(2-aminopropanoic acid)" EXACT RESID-systematic []
-synonym: "5'-(L-tyros-5'-yl)amino-L-tyrosine" EXACT RESID-name []
-synonym: "5'-[(tyros-5'-yl)amino]tyrosine" EXACT RESID-alternate []
-synonym: "5'-tyrosyl-5'-aminotyrosine" EXACT RESID-alternate []
-synonym: "bis(LTQ) linkage" EXACT RESID-alternate []
-synonym: "CROSSLNK 5'-tyrosyl-5'-aminotyrosine (Tyr-Tyr) (interchain)" EXACT UniProt-feature []
-property_value: DiffAvg "13.00" xsd:float
-property_value: DiffFormula "C 0 H -1 N 1 O 0" xsd:string
-property_value: DiffMono "12.995249" xsd:float
-property_value: Formula "C 18 H 17 N 3 O 4" xsd:string
-property_value: MassAvg "339.35" xsd:float
-property_value: MassMono "339.121906" xsd:float
-property_value: Origin "Y, Y" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: uniprot.ptm:PTM-0320
-is_a: MOD:00692
-is_a: MOD:02058
-
-[Term]
-id: MOD:01788
-name: histidine immonium ion
-def: "A protein modification that effectively converts an N-terminal L-histidine residue to histidine immonium ion." [PubMed:17074506, PubMed:18688235]
-comment: This fragment corresponds to the first ion in an a+ series.
-subset: PSI-MOD-slim
-synonym: "2-(1H-imidazolyl)ethaniminium" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "-27.00" xsd:float
-property_value: DiffFormula "C -1 H 1 N 0 O -1" xsd:string
-property_value: DiffMono "-26.987638" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 5 H 8 N 3 O 0" xsd:string
-property_value: MassAvg "110.14" xsd:float
-property_value: MassMono "110.071274" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00909
-is_a: MOD:01527
-
-[Term]
-id: MOD:01789
-name: phenylalanine immonium ion
-def: "A protein modification that effectively converts an N-terminal L-phenylalanine residue to phenylalanine immonium ion." [PubMed:17074506, PubMed:18688235]
-comment: This fragment corresponds to the first ion in an a+ series.
-subset: PSI-MOD-slim
-synonym: "2-phenylethaniminium" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "-27.00" xsd:float
-property_value: DiffFormula "C -1 H 1 N 0 O -1" xsd:string
-property_value: DiffMono "-26.987638" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 8 H 10 N 1 O 0" xsd:string
-property_value: MassAvg "120.17" xsd:float
-property_value: MassMono "120.080776" xsd:float
-property_value: Origin "F" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00914
-is_a: MOD:01527
-
-[Term]
-id: MOD:01790
-name: tyrosine immonium ion
-def: "A protein modification that effectively converts an an N-terminal L-tyrosine residue to tyrosine immonium ion." [PubMed:17074506, PubMed:18688235]
-comment: This fragment corresponds to the first ion in an a+ series.
-subset: PSI-MOD-slim
-synonym: "2-(4-hydroxyphenyl)ethaniminium" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "-27.00" xsd:float
-property_value: DiffFormula "C -1 H 1 N 0 O -1" xsd:string
-property_value: DiffMono "-26.987638" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 8 H 10 N 1 O 1" xsd:string
-property_value: MassAvg "136.17" xsd:float
-property_value: MassMono "136.075690" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00919
-is_a: MOD:01527
-
-[Term]
-id: MOD:01791
-name: phosphohistidine immonium ion
-def: "A protein modification that effectively converts an N-terminal phosphohistidine residue to phosphohistidine immonium ion." [PubMed:17690871, PubMed:18688235, PubMed:20847263]
-comment: This fragment corresponds to the first ion in an a+ series.
-subset: PSI-MOD-slim
-synonym: "2-(1H-imidazolyl)ethaniminium" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "-27.00" xsd:float
-property_value: DiffFormula "C -1 H 1 N 0 O -1" xsd:string
-property_value: DiffMono "-26.987638" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 5 H 9 N 3 O 3 P 1" xsd:string
-property_value: MassAvg "190.12" xsd:float
-property_value: MassMono "190.037604" xsd:float
-property_value: Origin "MOD:00890" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00909
-is_a: MOD:01527
-relationship: derives_from MOD:00890
-
-[Term]
-id: MOD:01792
-name: phosphotyrosine immonium ion
-def: "A protein modification that effectively converts an N-terminal O4'-phospho-L-tyrosine residue to tyrosine immonium ion." [PubMed:17690871, PubMed:18688235]
-comment: This fragment corresponds to the first ion in an a+ series.
-subset: PSI-MOD-slim
-synonym: "2-(4-phosphonoxyphenyl)ethaniminium" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "-27.00" xsd:float
-property_value: DiffFormula "C -1 H 1 N 0 O -1" xsd:string
-property_value: DiffMono "-26.987638" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 8 H 11 N 1 O 4 P 1" xsd:string
-property_value: MassAvg "216.15" xsd:float
-property_value: MassMono "216.042021" xsd:float
-property_value: Origin "MOD:00048" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00919
-is_a: MOD:01527
-relationship: derives_from MOD:00048
-
-[Term]
-id: MOD:01793
-name: S-carboxamidomethyl-L-cysteine sulfoxide
-def: "A protein modification that effectively converts an L-cysteine residue to S-carboxamidomethyl-L-cysteine sulfoxide." [PubMed:11212008, PubMed:17689096, PubMed:18306178, PubMed:18688235]
-synonym: "CamCO" EXACT PSI-MOD-alternate []
-synonym: "S-carbamoylmethyl-L-cysteine sulfoxide" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "73.05" xsd:float
-property_value: DiffFormula "C 2 H 3 N 1 O 2" xsd:string
-property_value: DiffMono "73.016378" xsd:float
-property_value: Formula "C 5 H 8 N 2 O 3 S 1" xsd:string
-property_value: MassAvg "176.19" xsd:float
-property_value: MassMono "176.025563" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00708
-is_a: MOD:01854
-relationship: derives_from MOD:01060
-
-[Term]
-id: MOD:01794
-name: 1x(13)C,3x(2)H labeled monomethylated residue
-def: "A protein modification that effectively replaces the methyl group of a residue containing common isotopes with a 1x(13)C,3x(2)H labeled monomethylated residue." [PubMed:18688235]
-synonym: "Methyl:2H(3)13C(1)" RELATED PSI-MS-label []
-property_value: DiffAvg "18.04" xsd:float
-property_value: DiffFormula "(13)C 1 (1)H -1 (2)H 3" xsd:string
-property_value: DiffMono "18.037835" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00839
-is_a: MOD:00842
-
-[Term]
-id: MOD:01795
-name: 1x(13)C,3x(2)H C(6)-labeled L-methionine
-def: "A protein modification that effectively converts an L-methionine residue containing common isotopes to 1x(13)C,3x(2)H C(6)-labeled L-methionine." [PubMed:15782174, PubMed:18688235]
-synonym: "Methyl:2H(3)13C(1)" RELATED PSI-MS-label []
-property_value: DiffAvg "4.02" xsd:float
-property_value: DiffFormula "(12)C -1 (13)C 1 (1)H -3 (2)H 3" xsd:string
-property_value: DiffMono "4.022185" xsd:float
-property_value: Formula "(12)C 4 (13)C 1 (1)H 6 (2)H 3 N 1 O 1 S 1" xsd:string
-property_value: MassAvg "135.06" xsd:float
-property_value: MassMono "135.062670" xsd:float
-property_value: Origin "M" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00839
-is_a: MOD:00842
-is_a: MOD:00913
-
-[Term]
-id: MOD:01796
-name: 1x(13)C,3x(2)H C(6)-labeled L-methionine sulfoxide
-def: "A protein modification that effectively converts an L-methionine residue containing common isotopes to 1x(13)C,3x(2)H C(6)-labeled L-methionine sulfoxide." [PubMed:15782174, PubMed:18688235]
-property_value: DiffAvg "20.02" xsd:float
-property_value: DiffFormula "(12)C -1 (13)C 1 (1)H -3 (2)H 3 O 1" xsd:string
-property_value: DiffMono "20.017100" xsd:float
-property_value: Formula "(12)C 4 (13)C 1 (1)H 6 (2)H 3 N 1 O 2 S 1" xsd:string
-property_value: MassAvg "151.06" xsd:float
-property_value: MassMono "151.057585" xsd:float
-property_value: Origin "M" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00839
-is_a: MOD:00913
-
-[Term]
-id: MOD:01797
-name: 1'-phosphohistidine immonium ion
-def: "A protein modification that effectively converts an N-terminal 1'-phosphohistidine residue to 1'-phosphohistidine immonium ion." [PubMed:17690871, PubMed:18688235, PubMed:20847263]
-comment: This fragment corresponds to the first ion in an a+ series.
-synonym: "2-((1-phosphono-1H-imidazol-4-yl)ethaniminium" EXACT PSI-MOD-alternate []
-synonym: "Ntau-phosphorylated L-histidine" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "-27.00" xsd:float
-property_value: DiffFormula "C -1 H 1 N 0 O -1" xsd:string
-property_value: DiffMono "-26.987638" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 5 H 9 N 3 O 3 P 1" xsd:string
-property_value: MassAvg "190.12" xsd:float
-property_value: MassMono "190.037604" xsd:float
-property_value: Origin "MOD:00044" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01791
-relationship: derives_from MOD:00044
-
-[Term]
-id: MOD:01798
-name: 3'-phosphohistidine immonium ion
-def: "A protein modification that effectively converts an N-terminal 3'-phosphohistidine residue to 3'-phosphohistidine immonium ion." [PubMed:18688235]
-comment: This fragment corresponds to the first ion in an a+ series.
-synonym: "2-(1-phosphono-1H-imidazol-5-yl)ethaniminium" EXACT PSI-MOD-alternate []
-synonym: "Npi-phosphorylated L-histidine" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "-27.00" xsd:float
-property_value: DiffFormula "C -1 H 1 N 0 O -1" xsd:string
-property_value: DiffMono "-26.987638" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 5 H 9 N 3 O 3 P 1" xsd:string
-property_value: MassAvg "190.12" xsd:float
-property_value: MassMono "190.037604" xsd:float
-property_value: Origin "MOD:00045" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01791
-relationship: derives_from MOD:00045
-
-[Term]
-id: MOD:01799
-name: methylated serine
-def: "A protein modification that effectively converts an L-alanine residue to a methylated serine, such as N-methylserine, N,N-dimethylserine, or N,N,N-trimethylserine." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "MeSer" EXACT PSI-MOD-label []
-property_value: Origin "S" xsd:string
-is_a: MOD:00427
-is_a: MOD:00916
-
-[Term]
-id: MOD:01800
-name: N-methylated serine
-def: "A protein modification that effectively replaces an L-serine alpha amino hydrogen with a methyl group." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:01460
-is_a: MOD:01799
-
-[Term]
-id: MOD:01801
-name: protonated L-serine (L-serinium) residue
-def: "A protein modification that effectively converts an L-serine residue to an L-serinium (protonated L-serine)." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: DiffAvg "1.01" xsd:float
-property_value: DiffFormula "C 0 H 1 N 0 O 0" xsd:string
-property_value: DiffMono "1.007276" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 3 H 7 N 1 O 2" xsd:string
-property_value: MassAvg "89.09" xsd:float
-property_value: MassMono "89.047130" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00916
-is_a: MOD:01700
-
-[Term]
-id: MOD:01802
-name: N,N,N-trimethyl-L-serine (from L-serinium)
-def: "A protein modification that effectively converts an L-serinium (protonated L-serine) residue to an N,N,N-trimethyl-L-serine." [PubMed:18688235]
-comment: For amino acids residues, amine trimethylation can effectively only be accomplished with an aminium, protonated primary amino, group. This process accounts only for trimethylation and not protonation. The alternative N2Me3+Ser process (MOD:00071) accounts for both protonation and trimethylation.
-subset: PSI-MOD-slim
-synonym: "N2Me3Ala" EXACT PSI-MOD-label []
-property_value: DiffAvg "42.08" xsd:float
-property_value: DiffFormula "C 3 H 6 N 0 O 0" xsd:string
-property_value: DiffMono "42.046402" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 6 H 13 N 1 O 2" xsd:string
-property_value: MassAvg "131.17" xsd:float
-property_value: MassMono "131.094080" xsd:float
-property_value: Origin "MOD:01801" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:01687
-relationship: derives_from MOD:01801
-
-[Term]
-id: MOD:01803
-name: O-methylated threonine
-def: "A protein modification that effectively converts an L-threonine residue to a methylated threonine, such as O-methyl-L-threonine or L-threonine methyl ester." [PubMed:18688235]
-synonym: "OMeThr" EXACT PSI-MOD-label []
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00393
-is_a: MOD:01418
-
-[Term]
-id: MOD:01804
-name: glycosylphosphorylated residue
-def: "A protein modification that effectively results from forming an adduct with a glycosylphosphate through a phosphodiester bond." [PubMed:18688235]
-is_a: MOD:00764
-is_a: MOD:00861
-
-[Term]
-id: MOD:01805
-name: N-(L-isoaspartyl)-glycine (Asp)
-def: "A protein modification that effectively crosslinks an L-aspartic acid residue and a glycine residue by an isopeptide bond with formation of N-(L-isoaspartyl)-glycine and the release of water." [ChEBI:21479, PubMed:1826288, PubMed:18671394, RESID:AA0126]
-comment: Cross-link 2.
-synonym: "(2S)-2-amino-4-(carboxymethyl)amino-4-oxobutanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-N4-(carboxymethyl)-butanediamic acid" EXACT RESID-alternate []
-synonym: "CROSSLNK Isoaspartyl glycine isopeptide (Asp-Gly)" EXACT UniProt-feature []
-synonym: "CROSSLNK Isoaspartyl glycine isopeptide (Gly-Asp)" EXACT UniProt-feature []
-synonym: "isoaspartyl glycine" EXACT RESID-alternate []
-synonym: "N-(L-isoaspartyl)-glycine" EXACT RESID-name []
-synonym: "N-beta-aspartylglycine" EXACT RESID-alternate []
-synonym: "N4-(carboxymethyl)-asparagine" EXACT RESID-alternate []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 6 H 7 N 2 O 3" xsd:string
-property_value: MassAvg "155.13" xsd:float
-property_value: MassMono "155.045667" xsd:float
-property_value: Origin "D, G" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0490
-is_a: MOD:02043
-is_a: MOD:00954
-is_a: MOD:01928
-
-[Term]
-id: MOD:01806
-name: N,N-dimethyl-L-leucine
-def: "A protein modification that effectively converts an L-leucine residue to N,N-dimethyl-L-leucine." [PubMed:19522542, RESID:AA0538]
-synonym: "(2S)-2-(dimethylamino)-4-methylpentanoic acid" EXACT RESID-systematic []
-synonym: "2-(dimethylamino)-4-methylvaleric acid" EXACT RESID-alternate []
-synonym: "2-(dimethylazanyl)-4-methylpentanoic acid" EXACT RESID-alternate []
-synonym: "MOD_RES N,N-dimethylleucine" EXACT UniProt-feature []
-synonym: "N,N-dimethyl-L-leucine" EXACT RESID-name []
-synonym: "N,N-dimethylleucine" EXACT RESID-alternate []
-property_value: DiffAvg "28.05" xsd:float
-property_value: DiffFormula "C 2 H 4 N 0 O 0" xsd:string
-property_value: DiffMono "28.031300" xsd:float
-property_value: Formula "C 8 H 16 N 1 O 1" xsd:string
-property_value: MassAvg "142.22" xsd:float
-property_value: MassMono "142.123189" xsd:float
-property_value: Origin "L" xsd:string
-property_value: Source "hypothetical" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0435
-is_a: MOD:01686
-is_a: MOD:01808
-
-[Term]
-id: MOD:01807
-name: N-formyl-L-glutamic acid
-def: "A protein modification that effectively converts an L-glutamic acid residue to N-formyl-L-glutamic acid." [PubMed:18001127, RESID:AA0539]
-synonym: "(2S)-2-(formylamino)pentanedioic acid" EXACT RESID-systematic []
-synonym: "2-(formylazanyl)pentanedioic acid" EXACT RESID-alternate []
-synonym: "2-formamidopentanedioic acid" EXACT RESID-alternate []
-synonym: "2-formylaminopentanedioic acid" EXACT RESID-alternate []
-synonym: "N-formyl-L-glutamic acid" EXACT RESID-name []
-property_value: DiffAvg "28.01" xsd:float
-property_value: DiffFormula "C 1 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "27.994915" xsd:float
-property_value: Formula "C 6 H 8 N 1 O 4" xsd:string
-property_value: MassAvg "158.13" xsd:float
-property_value: MassMono "158.045333" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00409
-is_a: MOD:00906
-
-[Term]
-id: MOD:01808
-name: N-methylated leucine
-def: "A protein modification that effectively replaces an L-leucine alpha amino hydrogen with a methyl group." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "MeLeu" EXACT PSI-MOD-label []
-property_value: Origin "L" xsd:string
-is_a: MOD:00662
-is_a: MOD:01460
-
-[Term]
-id: MOD:01809
-name: 5x(13)C,1x(15)N labeled residue
-def: "A protein modification that effectively converts a residue containing common isotopes to a 5x(13)C,1x(15)N labeled residue." [PubMed:12771378, Unimod:268]
-synonym: "13C(5) 15N(1) Silac label" RELATED Unimod-description []
-synonym: "Label:13C(5)15N(1)" RELATED PSI-MS-label []
-property_value: DiffAvg "6.01" xsd:float
-property_value: DiffFormula "(12)C -5 (13)C 5 (14)N -1 (15)N 1" xsd:string
-property_value: DiffMono "6.013809" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:268
-is_a: MOD:00842
-is_a: MOD:00843
-
-[Term]
-id: MOD:01810
-name: 5x(13)C,1x(15)N labeled L-proline
-def: "A protein modification that effectively converts an L-proline residue to 5x(13)C,1x(15)N labeled L-proline." [PubMed:12771378, Unimod:268#P]
-synonym: "13C(5) 15N(1) Silac label" RELATED Unimod-description []
-synonym: "Label:13C(5)15N(1)" RELATED PSI-MS-label []
-property_value: DiffAvg "6.01" xsd:float
-property_value: DiffFormula "(12)C -5 (13)C 5 (14)N -1 (15)N 1" xsd:string
-property_value: DiffMono "6.013809" xsd:float
-property_value: Formula "(13)C 5 H 7 (15)N 1 O 1" xsd:string
-property_value: MassAvg "103.07" xsd:float
-property_value: MassMono "103.066573" xsd:float
-property_value: Origin "P" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:268
-is_a: MOD:00915
-is_a: MOD:01809
-
-[Term]
-id: MOD:01811
-name: 5x(13)C,1x(15)N labeled L-methionine
-def: "A protein modification that effectively converts an L-methionine residue to 5x(13)C,1x(15)N labeled L-methionine." [PubMed:12771378, Unimod:268#M]
-synonym: "13C(5) 15N(1) Silac label" RELATED Unimod-description []
-synonym: "Label:13C(5)15N(1)" RELATED PSI-MS-label []
-property_value: DiffAvg "6.01" xsd:float
-property_value: DiffFormula "(12)C -5 (13)C 5 (14)N -1 (15)N 1" xsd:string
-property_value: DiffMono "6.013809" xsd:float
-property_value: Formula "(13)C 5 H 9 (15)N 1 O 1 S 1" xsd:string
-property_value: MassAvg "137.05" xsd:float
-property_value: MassMono "137.054294" xsd:float
-property_value: Origin "M" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:268
-is_a: MOD:00913
-is_a: MOD:01809
-
-[Term]
-id: MOD:01812
-name: 5x(13)C,1x(15)N labeled L-methionine sulfoxide
-def: "A protein modification that effectively converts an L-methionine residue to 5x(13)C,1x(15)N labeled L-methionine sulfoxide." [PubMed:12771378, Unimod:268#M]
-synonym: "13C(5) 15N(1) Silac label" RELATED Unimod-description []
-synonym: "Label:13C(5)15N(1)" RELATED PSI-MS-label []
-property_value: DiffAvg "6.01" xsd:float
-property_value: DiffFormula "(12)C -5 (13)C 5 (14)N -1 (15)N 1" xsd:string
-property_value: DiffMono "6.013809" xsd:float
-property_value: Formula "(13)C 5 H 9 (15)N 1 O 2 S 1" xsd:string
-property_value: MassAvg "153.05" xsd:float
-property_value: MassMono "153.049209" xsd:float
-property_value: Origin "M" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:268
-relationship: derives_from MOD:00719
-is_a: MOD:01809
-
-[Term]
-id: MOD:01813
-name: morpholine-2-acetylated residue
-def: "A protein modification that effectively substitutes a morpholine-2-acetyl group for a hydrogen atom." [PubMed:10446193, Unimod:29]
-comment: The Unimod name \"N-Succinimidyl-3-morpholine acetate\" appears to have been a typographical error [JSG].
-synonym: "N-Succinimidyl-2-morpholine acetate" RELATED Unimod-description []
-synonym: "N-succinimidylmorpholine-2-acetate derivative" EXACT PSI-MOD-alternate []
-synonym: "SMA" RELATED PSI-MS-label []
-property_value: DiffAvg "127.14" xsd:float
-property_value: DiffFormula "C 6 H 9 N 1 O 2" xsd:string
-property_value: DiffMono "127.063329" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:29
-is_a: MOD:00649
-is_a: MOD:00848
-
-[Term]
-id: MOD:01814
-name: L-cysteine 3-hydroxy-2,5-pyridinedicarboxylic acid
-def: "A protein modification that effectively cross-links a cysteine and two serine residues to form L-cysteine 3-hydroxy-2,5-pyridinedicarboxylic acid." [PubMed:18406324, PubMed:19678698, PubMed:893891, RESID:AA0540]
-comment: Cross-link 3.
-synonym: "6-[(1R)-1-amino-2-sulfanylethyl]-3-hydroxypyridine-2,5-dicarboxylic acid" EXACT RESID-systematic []
-synonym: "6-[1-azanyl-2-sulfanylethyl]-3-hydroxypyridine-2,5-dicarboxylic acid" EXACT RESID-alternate []
-synonym: "L-cysteine 3-hydroxy-2,5-pyridinedicarboxylic acid" EXACT RESID-name []
-synonym: "CROSSLNK 3-hydroxypyridine-2,5-dicarboxylic acid (Ser-Cys)" RELATED UniProt-feature []
-property_value: DiffAvg "-54.07" xsd:float
-property_value: DiffFormula "C 0 H -8 N -1 O -2 S 0" xsd:string
-property_value: DiffMono "-54.055504" xsd:float
-property_value: Formula "C 9 H 7 N 2 O 3 S 1" xsd:string
-property_value: MassAvg "223.23" xsd:float
-property_value: MassMono "223.017738" xsd:float
-property_value: Origin "C, S, S" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0454
-is_a: MOD:02044
-is_a: MOD:02055
-is_a: MOD:01425
-
-[Term]
-id: MOD:01815
-name: L-glutamate thiazole-4-carboxylic acid
-def: "A protein modification that effectively crosslinks an L-cysteine residue and an L-glutamic acid residue to form L-glutamate thiazole-4-carboxylic acid." [PubMed:18406324, PubMed:19678698, PubMed:893891, RESID:AA0541]
-comment: Cross-link 2.
-synonym: "2-[(1S)-1-amino-3-carboxypropyl]-1,3-thiazole-4-carboxylic acid" EXACT RESID-systematic []
-synonym: "2-[-1-azanyl-3-carboxypropyl]-1,3-thiazole-4-carboxylic acid" EXACT RESID-alternate []
-synonym: "CROSSLNK Thiazole-4-carboxylic acid (Glu-Cys)" EXACT UniProt-feature []
-synonym: "L-glutamate thiazole-4-carboxylic acid" EXACT RESID-name []
-property_value: DiffAvg "-20.03" xsd:float
-property_value: DiffFormula "C 0 H -4 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-20.026215" xsd:float
-property_value: Formula "C 8 H 8 N 2 O 3 S 1" xsd:string
-property_value: MassAvg "212.22" xsd:float
-property_value: MassMono "212.025563" xsd:float
-property_value: Origin "C, E" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0456
-is_a: MOD:02045
-is_a: MOD:01420
-is_a: MOD:02082
-
-[Term]
-id: MOD:01816
-name: 2'-hydroxy-L-tryptophan
-def: "A protein modification that effectively converts an L-tryptophan residue to a 2'-hydroxy-L-tryptophan." [PubMed:11714714, RESID:AA0542]
-synonym: "(2S)-2-amino-3-(2-hydroxy-1H-indol-3-yl)propanoic acid" EXACT RESID-systematic []
-synonym: "2'-hydroxy-L-tryptophan" EXACT RESID-name []
-synonym: "2-azanyl-3-(2-hydroxy-1H-indol-3-yl)propanoic acid" EXACT RESID-alternate []
-synonym: "2-hydroxy-L-tryptophan" EXACT RESID-alternate []
-synonym: "2-hydroxy-tryptophan" EXACT RESID-alternate []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 11 H 10 N 2 O 2" xsd:string
-property_value: MassAvg "202.21" xsd:float
-property_value: MassMono "202.074228" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01622
-
-[Term]
-id: MOD:01817
-name: 2'-oxo-L-tryptophan
-def: "A protein modification that effectively converts an L-tryptophan residue to a 2'-oxo-L-tryptophan." [PubMed:9461080, RESID:AA0543]
-synonym: "(2S)-2-amino-3-[(3S)-2-oxo-2,3-dihydro-1H-indol-3-yl]propanoic acid" EXACT RESID-systematic []
-synonym: "2'-oxo-L-tryptophan" EXACT RESID-name []
-synonym: "2-azanyl-3-[(3S)-2-oxo-2,3-dihydro-1H-indol-3-yl]propanoic acid" EXACT RESID-alternate []
-synonym: "2-oxo-L-tryptophan" EXACT RESID-alternate []
-synonym: "2-oxotryptophan" EXACT RESID-alternate []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 11 H 10 N 2 O 2" xsd:string
-property_value: MassAvg "202.21" xsd:float
-property_value: MassMono "202.074228" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00679
-is_a: MOD:00918
-
-[Term]
-id: MOD:01818
-name: 1'-(L-tryptophan-3'-yl)-L-tryptophan
-def: "A protein modification that effectively cross-links two tryptophan residues to form 1'-(L-tryptophan-3'-yl)-L-tryptophan." [PubMed:20600836, RESID:AA0544]
-comment: Cross-link 2.
-synonym: "(2S,2'S)-3,3'-(3'H-1,3'-biindole-3,3'-diyl)bis(2-aminopropanoic acid)" EXACT RESID-alternate []
-synonym: "1-(L-tryptophan-3-yl)-L-tryptophan" EXACT RESID-name []
-synonym: "2-amino-3-[2-[2-amino-3-(2-carboxyethyl)-1H-indol-4-yl]-1H-indol-3-yl]propanoic acid" EXACT RESID-alternate []
-synonym: "3-[(2S)-2-amino-2-carboxyethyl]-3-(3-[(2S)-2-amino-2-carboxyethyl]-1H-indol-2-yl)-1H-indole" EXACT RESID-systematic []
-synonym: "3-[2-azanyl-2-carboxyethyl]-3-(3-[2-azanyl-2-carboxyethyl]-1H-indol-2-yl)-1H-indole" EXACT RESID-alternate []
-synonym: "ditryptophan" EXACT RESID-alternate []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 22 H 18 N 4 O 2" xsd:string
-property_value: MassAvg "370.41" xsd:float
-property_value: MassMono "370.142976" xsd:float
-property_value: Origin "W, W" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0544
-is_a: MOD:00692
-is_a: MOD:02057
-
-[Term]
-id: MOD:01819
-name: N6-succinyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-succinyl-L-lysine." [PubMed:16582421, PubMed:21151122, RESID:AA0545]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-6-[(3-carboxypropanoyl)amino]hexanoic acid" EXACT RESID-systematic []
-synonym: "2-azanyl-6-[(3-carboxypropanoyl)azanyl]hexanoic acid" EXACT RESID-alternate []
-synonym: "4-[[(5S)-5-amino-6-hydroxy-6-oxohexyl]amino]-4-oxobutanoate" EXACT RESID-alternate []
-synonym: "MOD_RES N6-succinyllysine" EXACT UniProt-feature []
-synonym: "N(epsilon)-(succinyl)lysine" EXACT RESID-alternate []
-synonym: "N6-succinyl-L-lysine" EXACT RESID-name []
-synonym: "succinyllysine" EXACT RESID-alternate []
-property_value: DiffAvg "100.07" xsd:float
-property_value: DiffFormula "C 4 H 4 N 0 O 3" xsd:string
-property_value: DiffMono "100.016044" xsd:float
-property_value: Formula "C 10 H 16 N 2 O 4" xsd:string
-property_value: MassAvg "228.25" xsd:float
-property_value: MassMono "228.111007" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0438
-is_a: MOD:01029
-is_a: MOD:01875
-
-[Term]
-id: MOD:01820
-name: isotope tagged sufhydryl reagent modified cysteine
-def: "A protein modification that effectively replaces a cysteine sulhydryl hydrogen with an isotope tagged sulfhydryl reagent group." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00905
-is_a: MOD:01426
-
-[Term]
-id: MOD:01821
-name: cysTMT6plex reporter+balance reagent cysteine disulfide
-def: "A protein modification that effectively replaces a residue sulfhydryl hydrogen with a Thermo Scientific cysTMT6plex reporter+balance group." [Unimod:985, URL:http\://www.piercenet.com/files/2162220.pdf]
-comment: The reagent consists of a reporter group, a balance group and a protein sulfhydryl reactive pyridine disulfanyl group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "cysteine-reactive Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "cysTMT6plex" RELATED Unimod-interim []
-synonym: "S-(2-{3-[2-(2,6-dimethylpiperidin-1-yl)acetamido]propanamido}ethyl)sulfanyl" EXACT PSI-MOD-alternate []
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:985
-is_a: MOD:01428
-is_a: MOD:01429
-is_a: MOD:01820
-
-[Term]
-id: MOD:01822
-name: cysTMT6plex-zero reporter+balance reagent cysteine disulfide
-def: "A protein modification that effectively replaces a residue sulfhydryl hydrogen with a Thermo Scientific cysTMT6plex-zero reporter+balance group." [Unimod:984, URL:http\://www.piercenet.com/files/2162220.pdf]
-comment: The reagent consists of a reporter group, a balance group and a protein sulfhydryl reactive pyridine disulfanyl group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "cysTMT" RELATED Unimod-interim []
-synonym: "Native cysteine-reactive Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "S-(2-{3-[2-(2,6-dimethylpiperidin-1-yl)acetamido]propanamido}ethyl)sulfanyl" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "299.17" xsd:float
-property_value: DiffFormula "(12)C 14 H 25 (14)N 3 O 2 S 1" xsd:string
-property_value: DiffMono "299.166748" xsd:float
-property_value: Formula "(12)C 17 H 32 (14)N 4 O 4 S 2" xsd:string
-property_value: MassAvg "420.19" xsd:float
-property_value: MassMono "420.186498" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:984
-is_a: MOD:01821
-
-[Term]
-id: MOD:01823
-name: cysTMT6plex-126 reporter+balance reagent cysteine disulfide
-def: "A protein modification that effectively replaces a residue sulfhydryl hydrogen with a Thermo Scientific cysTMT6plex-126 reporter+balance group." [PubMed:18688235, URL:http\://www.piercenet.com/files/2162220.pdf]
-comment: The reagent consists of a reporter group, a balance group and a protein sulfhydryl reactive pyridine disulfanyl group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "cysteine-reactive Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "cysTMT6plex" RELATED Unimod-interim []
-synonym: "S-(2-{3-[2-(2,6-dimethylpiperidin-1-yl)acetamido]propanamido}ethyl)sulfanyl" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "304.18" xsd:float
-property_value: DiffFormula "(12)C 10 (13)C 4 H 25 (14)N 2 (15)N 1 O 2 S 1" xsd:string
-property_value: DiffMono "304.177202" xsd:float
-property_value: Formula "(12)C 13 (13)C 4 H 32 (14)N 3 (15)N 1 O 4 S 2" xsd:string
-property_value: MassAvg "425.20" xsd:float
-property_value: MassMono "425.196952" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:985
-is_a: MOD:01821
-
-[Term]
-id: MOD:01824
-name: cysTMT6plex-127 reporter+balance reagent cysteine disulfide
-def: "A protein modification that effectively replaces a residue sulfhydryl hydrogen with a Thermo Scientific cysTMT6plex-127 reporter+balance group." [PubMed:18688235, URL:http\://www.piercenet.com/files/2162220.pdf]
-comment: The reagent consists of a reporter group, a balance group and a protein sulfhydryl reactive pyridine disulfanyl group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "cysteine-reactive Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "cysTMT6plex" RELATED Unimod-interim []
-synonym: "S-(2-{3-[2-(2,6-dimethylpiperidin-1-yl)acetamido]propanamido}ethyl)sulfanyl" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "304.18" xsd:float
-property_value: DiffFormula "(12)C 10 (13)C 4 H 25 (14)N 2 (15)N 1 O 2 S 1" xsd:string
-property_value: DiffMono "304.177202" xsd:float
-property_value: Formula "(12)C 13 (13)C 4 H 32 (14)N 3 (15)N 1 O 4 S 2" xsd:string
-property_value: MassAvg "425.20" xsd:float
-property_value: MassMono "425.196952" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01821
-
-[Term]
-id: MOD:01825
-name: cysTMT6plex-128 reporter+balance reagent cysteine disulfide
-def: "A protein modification that effectively replaces a residue sulfhydryl hydrogen with a Thermo Scientific cysTMT6plex-128 reporter+balance group." [PubMed:18688235, URL:http\://www.piercenet.com/files/2162220.pdf]
-comment: The reagent consists of a reporter group, a balance group and a protein sulfhydryl reactive pyridine disulfanyl group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "cysteine-reactive Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "cysTMT6plex" RELATED Unimod-interim []
-synonym: "S-(2-{3-[2-(2,6-dimethylpiperidin-1-yl)acetamido]propanamido}ethyl)sulfanyl" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "304.18" xsd:float
-property_value: DiffFormula "(12)C 10 (13)C 4 H 25 (14)N 2 (15)N 1 O 2 S 1" xsd:string
-property_value: DiffMono "304.177202" xsd:float
-property_value: Formula "(12)C 13 (13)C 4 H 32 (14)N 3 (15)N 1 O 4 S 2" xsd:string
-property_value: MassAvg "425.20" xsd:float
-property_value: MassMono "425.196952" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01821
-
-[Term]
-id: MOD:01826
-name: cysTMT6plex-129 reporter+balance reagent cysteine disulfide
-def: "A protein modification that effectively replaces a residue sulfhydryl hydrogen with a Thermo Scientific cysTMT6plex-129 reporter+balance group." [PubMed:18688235, URL:http\://www.piercenet.com/files/2162220.pdf]
-comment: The reagent consists of a reporter group, a balance group and a protein sulfhydryl reactive pyridine disulfanyl group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "cysteine-reactive Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "cysTMT6plex" RELATED Unimod-interim []
-synonym: "S-(2-{3-[2-(2,6-dimethylpiperidin-1-yl)acetamido]propanamido}ethyl)sulfanyl" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "304.18" xsd:float
-property_value: DiffFormula "(12)C 10 (13)C 4 H 25 (14)N 2 (15)N 1 O 2 S 1" xsd:string
-property_value: DiffMono "304.177202" xsd:float
-property_value: Formula "(12)C 13 (13)C 4 H 32 (14)N 3 (15)N 1 O 4 S 2" xsd:string
-property_value: MassAvg "425.20" xsd:float
-property_value: MassMono "425.196952" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01821
-
-[Term]
-id: MOD:01827
-name: cysTMT6plex-130 reporter+balance reagent cysteine disulfide
-def: "A protein modification that effectively replaces a residue sulfhydryl hydrogen with a Thermo Scientific cysTMT6plex-130 reporter+balance group." [PubMed:18688235, URL:http\://www.piercenet.com/files/2162220.pdf]
-comment: The reagent consists of a reporter group, a balance group and a protein sulfhydryl reactive pyridine disulfanyl group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "cysteine-reactive Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "cysTMT6plex" RELATED Unimod-interim []
-synonym: "S-(2-{3-[2-(2,6-dimethylpiperidin-1-yl)acetamido]propanamido}ethyl)sulfanyl" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "304.18" xsd:float
-property_value: DiffFormula "(12)C 10 (13)C 4 H 25 (14)N 2 (15)N 1 O 2 S 1" xsd:string
-property_value: DiffMono "304.177202" xsd:float
-property_value: Formula "(12)C 13 (13)C 4 H 32 (14)N 3 (15)N 1 O 4 S 2" xsd:string
-property_value: MassAvg "425.20" xsd:float
-property_value: MassMono "425.196952" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01821
-
-[Term]
-id: MOD:01828
-name: cysTMT6plex-131 reporter+balance reagent cysteine disulfide
-def: "A protein modification that effectively replaces a residue sulfhydryl hydrogen with a Thermo Scientific cysTMT6plex-131 reporter+balance group." [PubMed:18688235, URL:http\://www.piercenet.com/files/2162220.pdf]
-comment: The reagent consists of a reporter group, a balance group and a protein sulfhydryl reactive pyridine disulfanyl group. The reporter group, an isotopically labeled 1,2,6-trimethylpiperidine, is connected to a 3-(carbonylamino)propanoyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "cysteine-reactive Sixplex Tandem Mass Tag(TM)" RELATED Unimod-description []
-synonym: "cysTMT6plex" RELATED Unimod-interim []
-synonym: "S-(2-{3-[2-(2,6-dimethylpiperidin-1-yl)acetamido]propanamido}ethyl)sulfanyl" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "304.18" xsd:float
-property_value: DiffFormula "(12)C 10 (13)C 4 H 25 (14)N 2 (15)N 1 O 2 S 1" xsd:string
-property_value: DiffMono "304.177202" xsd:float
-property_value: Formula "(12)C 13 (13)C 4 H 32 (14)N 3 (15)N 1 O 4 S 2" xsd:string
-property_value: MassAvg "425.20" xsd:float
-property_value: MassMono "425.196952" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01821
-
-[Term]
-id: MOD:01829
-name: S-carboxymethyl-L-cysteine sulfoxide
-def: "A protein modification that effectively converts an L-cysteine residue to S-carboxymethyl-L-cysteine sulfoxide." [PubMed:17689096, PubMed:18688235]
-synonym: "CmCO" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "58.04" xsd:float
-property_value: DiffFormula "C 2 H 2 N 0 O 2 S 0" xsd:string
-property_value: DiffMono "58.005479" xsd:float
-property_value: Formula "C 5 H 7 N 1 O 3 S 1" xsd:string
-property_value: MassAvg "161.18" xsd:float
-property_value: MassMono "161.014664" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00399
-is_a: MOD:00708
-is_a: MOD:01854
-relationship: derives_from MOD:01061
-
-[Term]
-id: MOD:01830
-name: S-carboxymethyl-L-cysteine sulfone
-def: "A protein modification that effectively converts an L-cysteine residue to S-carboxymethyl-L-cysteine sulfone." [PubMed:18688235]
-synonym: "CmCO2" EXACT PSI-MOD-label []
-property_value: DiffAvg "74.03" xsd:float
-property_value: DiffFormula "C 2 H 2 N 0 O 3 S 0" xsd:string
-property_value: DiffMono "74.000394" xsd:float
-property_value: Formula "C 5 H 7 N 1 O 4 S 1" xsd:string
-property_value: MassAvg "177.17" xsd:float
-property_value: MassMono "177.009579" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00708
-is_a: MOD:01855
-relationship: derives_from MOD:01061
-
-[Term]
-id: MOD:01831
-name: S-carboxamidomethyl-L-cysteine sulfone
-def: "A protein modification that effectively converts an L-cysteine residue to S-carboxamidomethyl-L-cysteine sulfone." [PubMed:18688235]
-synonym: "CamCO2" EXACT PSI-MOD-label []
-synonym: "S-carbamoylmethyl-L-cysteine sulfone" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "89.05" xsd:float
-property_value: DiffFormula "C 2 H 3 N 1 O 3" xsd:string
-property_value: DiffMono "89.011293" xsd:float
-property_value: Formula "C 5 H 8 N 2 O 4 S 1" xsd:string
-property_value: MassAvg "192.19" xsd:float
-property_value: MassMono "192.020478" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00708
-is_a: MOD:01855
-relationship: derives_from MOD:01060
-
-[Term]
-id: MOD:01832
-name: 5x(13)C-labeled residue
-def: "A protein modification that effectively converts a residue containing common isotopes to a 5x(13)C-labeled residue." [PubMed:12771378, Unimod:772]
-synonym: "13C(5) Silac label" RELATED Unimod-description []
-synonym: "Label:13C(5)" RELATED PSI-MS-label []
-property_value: DiffAvg "5.02" xsd:float
-property_value: DiffFormula "(12)C -5 (13)C 5" xsd:string
-property_value: DiffMono "5.016774" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:772
-is_a: MOD:00842
-
-[Term]
-id: MOD:01833
-name: 5x(13)C-labeled L-methionine
-def: "A protein modification that effectively converts an L-methionine residue containing common isotopes to 5x(13)C-labeled L-methionine." [PubMed:18688235, url:]
-property_value: DiffAvg "5.02" xsd:float
-property_value: DiffFormula "(12)C -5 (13)C 5 H 0 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "5.016774" xsd:float
-property_value: Formula "(13)C 5 H 9 N 1 O 1 S 1" xsd:string
-property_value: MassAvg "136.06" xsd:float
-property_value: MassMono "136.057259" xsd:float
-property_value: Origin "M" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00913
-is_a: MOD:01832
-
-[Term]
-id: MOD:01834
-name: 5x(13)C-labeled L-methionine sulfoxide
-def: "A protein modification that effectively converts an L-methionine residue containing common isotopes to 5x(13)C-labeled L-methionine sulfoxide." [PubMed:18688235]
-property_value: DiffAvg "5.02" xsd:float
-property_value: DiffFormula "(12)C -5 (13)C 5 H 0 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "5.016774" xsd:float
-property_value: Formula "(13)C 5 H 9 N 1 O 2 S 1" xsd:string
-property_value: MassAvg "152.05" xsd:float
-property_value: MassMono "152.052174" xsd:float
-property_value: Origin "MOD:00719" xsd:string
-property_value: Source "artifact" xsd:string
-relationship: derives_from MOD:00719
-is_a: MOD:01832
-
-[Term]
-id: MOD:01835
-name: 5x(13)C-labeled L-methionine sulfone
-def: "A protein modification that effectively converts an L-methionine residue containing common isotopes to 5x(13)C-labeled L-methionine sulfone." [PubMed:18688235]
-property_value: DiffAvg "5.02" xsd:float
-property_value: DiffFormula "(12)C -5 (13)C 5 H 0 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "5.016774" xsd:float
-property_value: Formula "(13)C 5 H 9 N 1 O 3 S 1" xsd:string
-property_value: MassAvg "168.05" xsd:float
-property_value: MassMono "168.047088" xsd:float
-property_value: Origin "MOD:00256" xsd:string
-property_value: Source "artifact" xsd:string
-relationship: derives_from MOD:00256
-is_a: MOD:01832
-
-[Term]
-id: MOD:01836
-name: N6-[([1-(6-nitro-2H-1,3-benzodioxol-5-yl)ethoxy]carbonyl]lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-[([1-(6-nitro-2H-1,3-benzodioxol-5-yl)ethoxy]carbonyl]lysine." [PubMed:18688235, PubMed:20218600, PubMed:21271704]
-synonym: "(2S)-2-amino-6-[([1-(6-nitro-1,3-benzodioxol-5-yl)ethoxy]carbonyl)amino]hexanoic acid" EXACT PSI-MOD-alternate []
-synonym: "[(alpha-methyl-6-nitro-piperonyloxy)carbonyl]lysine" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "237.17" xsd:float
-property_value: DiffFormula "C 10 H 7 N 1 O 6" xsd:string
-property_value: DiffMono "237.027337" xsd:float
-property_value: Formula "C 16 H 19 N 3 O 7" xsd:string
-property_value: MassAvg "365.34" xsd:float
-property_value: MassMono "365.122300" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00848
-is_a: MOD:01875
-
-[Term]
-id: MOD:01837
-name: L-lanthionine (Cys-Cys)
-def: "A protein modification that effectively cross-links two L-cysteine residues with a thioether bond to form L-lanthionine." [ChEBI:21347, PubMed:20805503, PubMed:6007887, RESID:AA0110#CYS2]
-comment: Cross-link 2.
-synonym: "(2R,2'R)-3,3'-sulfanediylbis(2-aminopropanoic acid)" EXACT RESID-systematic []
-synonym: "(R)-S-(2-amino-2-carboxyethyl)-L-cysteine" EXACT RESID-alternate []
-synonym: "(R,R)-2,6-diamino-4-thiaheptanedioic acid" EXACT RESID-alternate []
-synonym: "(R,R)-3,3'-thiobis-(2-aminopropanoic acid)" EXACT RESID-alternate []
-synonym: "(R,R)-bis(2-amino-2-carboxyethyl)sulfide" EXACT RESID-alternate []
-synonym: "2-amino-3-(2-amino-2-carboxyethyl)sulfanylpropanoic acid" EXACT RESID-alternate []
-synonym: "3,3'-thiobis-L-alanine" EXACT RESID-alternate []
-synonym: "L-lanthionine" EXACT RESID-name []
-property_value: DiffAvg "-34.08" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0 S -1" xsd:string
-property_value: DiffMono "-33.987721" xsd:float
-property_value: Formula "C 6 H 8 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "172.20" xsd:float
-property_value: MassMono "172.030649" xsd:float
-property_value: Origin "C, C" xsd:string
-property_value: Source "hypothetical" xsd:string
-is_a: MOD:00687
-
-[Term]
-id: MOD:01838
-name: L-lysinoalanine (Lys)
-def: "A protein modification that effectively converts an L-lysine residue to L-lysinoalanine." [PubMed:19155267, PubMed:2544544, RESID:AA0123#LYS]
-comment: This entry is for the modification of peptidyl lysine by a free serine. For the crosslink of peptidyl serine and peptidyl lysine see MOD:00132.
-synonym: "(2R,9S)-lysinoalanine" EXACT RESID-alternate []
-synonym: "(2S)-2-amino-6-([(2R)-2-amino-2-carboxyethyl]amino)hexanoic acid" EXACT RESID-systematic []
-synonym: "alaninolysine" EXACT RESID-alternate []
-synonym: "L-lysinoalanine" EXACT RESID-name []
-synonym: "LAL" EXACT RESID-alternate []
-synonym: "lysino-D-alanine" EXACT RESID-alternate []
-synonym: "MOD_RES Lysino-D-alanine (Lys)" EXACT UniProt-feature []
-synonym: "N-epsilon-(2-amino-2-carboxyethyl)-L-lysine" EXACT RESID-alternate []
-synonym: "N6-(2-amino-2-carboxyethyl)-L-lysine" EXACT RESID-alternate []
-property_value: DiffAvg "87.08" xsd:float
-property_value: DiffFormula "C 3 H 5 N 1 O 2" xsd:string
-property_value: DiffMono "87.032028" xsd:float
-property_value: Formula "C 9 H 17 N 3 O 3" xsd:string
-property_value: MassAvg "215.25" xsd:float
-property_value: MassMono "215.126991" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0439
-is_a: MOD:01853
-
-[Term]
-id: MOD:01839
-name: L-lanthionine
-def: "A protein modification that effectively cross-links either two L-cysteine residues, or an L-cysteine residue and an L-serine residue by a thioether bond to form L-lanthionine." [PubMed:18688235]
-comment: Cross-link 2. For the natural form of the lanthionine cross-link see MOD:00120 meso-lanthionine [JSG].
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 6 H 8 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "172.20" xsd:float
-property_value: MassMono "172.030649" xsd:float
-property_value: Origin "C, X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00859
-is_a: MOD:01841
-is_a: MOD:00954
-
-[Term]
-id: MOD:01840
-name: L-allo-isoleucine
-def: "A protein modification that effectively converts an L-isoleucine residue to L-allo-isoleucine." [ChEBI:43433, PubMed:20805503, RESID:AA0546]
-synonym: "(2S,3R)-2-amino-3-methylpentanoic acid" EXACT RESID-systematic []
-synonym: "2-azanyl-3-methylpentanoic acid" EXACT RESID-alternate []
-synonym: "3-methyl-norvaline" EXACT RESID-alternate []
-synonym: "allo-L-isoleucine" EXACT RESID-alternate []
-synonym: "alpha-amino-beta-methylvaleric acid" EXACT RESID-alternate []
-synonym: "L-allo-isoleucine" EXACT RESID-name []
-synonym: "L-threo-isoleucine" EXACT RESID-alternate []
-synonym: "MOD_RES L-allo-isoleucine" EXACT UniProt-feature []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 6 H 11 N 1 O 1" xsd:string
-property_value: MassAvg "113.16" xsd:float
-property_value: MassMono "113.084064" xsd:float
-property_value: Origin "I" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0442
-is_a: MOD:00664
-is_a: MOD:00910
-is_a: MOD:00306
-
-[Term]
-id: MOD:01841
-name: lanthionine
-def: "A protein modification that effectively cross-links either two or an L-cysteine residue and an L-serine residue by a thioether bond to form a lanthionine, either D- or L- or meso-lanthionine." [PubMed:18688235]
-comment: Cross-link 2. [JSG].
-synonym: "2,6-diamino-4-thiaheptanedioic acid" EXACT PSI-MOD-alternate []
-synonym: "2-amino-3-(2-amino-2-carboxyethyl)sulfanylpropanoic acid" EXACT PSI-MOD-alternate []
-synonym: "3,3'-thiobis-(2-aminopropanoic acid)" EXACT PSI-MOD-alternate []
-synonym: "3,3'-thiobis-L-alanine" EXACT PSI-MOD-alternate []
-synonym: "bis(2-amino-2-carboxyethyl)sulfanediyl" EXACT PSI-MOD-alternate []
-synonym: "bis(2-amino-2-carboxyethyl)sulfide" EXACT PSI-MOD-alternate []
-synonym: "S-(2-amino-2-carboxyethyl)-L-cysteine" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 6 H 8 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "172.20" xsd:float
-property_value: MassMono "172.030649" xsd:float
-property_value: Origin "C, X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01993
-is_a: MOD:00954
-
-[Term]
-id: MOD:01842
-name: S-(2-aminovinyl)-L-cysteine
-def: "A protein modification that effectively converts two L-cysteine residues to S-(2-aminovinyl)-L-cysteine." [PubMed:20805503, RESID:AA0548]
-comment: Cross-link 2.
-synonym: "(2R)-2-amino-3-([(Z)-2-aminoethenyl]sulfanyl)propanoic acid" EXACT RESID-systematic []
-synonym: "(R,Z)-S-(2-aminovinyl)cysteine" EXACT RESID-alternate []
-synonym: "S-(2-aminovinyl)-L-cysteine" EXACT RESID-name []
-property_value: DiffAvg "-80.10" xsd:float
-property_value: DiffFormula "C -1 H -4 N 0 O -2 S -1" xsd:string
-property_value: DiffMono "-79.993200" xsd:float
-property_value: Formula "C 5 H 7 N 2 O 1 S 1" xsd:string
-property_value: MassAvg "143.18" xsd:float
-property_value: MassMono "143.027909" xsd:float
-property_value: Origin "C, C" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0443
-is_a: MOD:01851
-
-[Term]
-id: MOD:01843
-name: 5'-chloro-L-tryptophan
-def: "A protein modification that effectively converts an L-tryptophan residue to 5'-chloro-L-tryptophan." [PubMed:18215770, RESID:AA0549]
-synonym: "(2S)-2-amino-3-(5-chloro-1H-indol-3-yl)propanoic acid" EXACT RESID-systematic []
-synonym: "5'-chloro-L-tryptophan" EXACT RESID-name []
-synonym: "MOD_RES 5'-chlorotryptophan" EXACT UniProt-feature []
-property_value: DiffAvg "34.44" xsd:float
-property_value: DiffFormula "C 0 Cl 1 H -1 N 0 O 0" xsd:string
-property_value: DiffMono "33.961028" xsd:float
-property_value: Formula "C 11 Cl 1 H 9 N 2 O 1" xsd:string
-property_value: MassAvg "220.66" xsd:float
-property_value: MassMono "220.040341" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0444
-is_a: MOD:01913
-
-[Term]
-id: MOD:01844
-name: 2-(3-methylbutanoyl)-5-hydroxyoxazole-4-carbothionic acid
-def: "A protein modification that effectively converts an L-cysteine residue and an L-leucine residue to 2-(3-methylbutanoyl)-5-hydroxyoxazole-4-carbothionic acid." [PubMed:15361623, PubMed:18729522, PubMed:20961038, PubMed:21254756, RESID:AA0550]
-comment: Cross-link 2.
-synonym: "(4Z)-4-[hydroxy(sulfanyl)methylidene]-2-(3-methylbutanoyl)-1,3-oxazol-5(4H)-one [tautomer]" EXACT RESID-alternate []
-synonym: "2-(3-methylbutanoyl)-5-hydroxyoxazole-4-carbothionic acid" EXACT RESID-name []
-synonym: "5-hydroxy-2-(3-methylbutanoyl)-1,3-oxazole-4-carbothioic O-acid" EXACT RESID-systematic []
-synonym: "MOD_RES 2-(3-methylbutanoyl)-5-hydroxyoxazole-4-carbothionic acid (Leu-Cys)" EXACT UniProt-feature []
-property_value: DiffAvg "-5.06" xsd:float
-property_value: DiffFormula "C 0 H -7 N -1 O 1 S 0" xsd:string
-property_value: DiffMono "-5.062935" xsd:float
-property_value: Formula "C 9 H 10 N 1 O 3 S 1" xsd:string
-property_value: MassAvg "212.24" xsd:float
-property_value: MassMono "212.038139" xsd:float
-property_value: Origin "C, L" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0448
-is_a: MOD:02044
-is_a: MOD:02050
-is_a: MOD:01856
-
-[Term]
-id: MOD:01845
-name: L-proline 5-hydroxyoxazole-4-carbothionic acid
-def: "A protein modification that effectively converts an L-cysteine residue and an L-proline residue to L-proline 5-hydroxyoxazole-4-carbothionic acid." [PubMed:15361623, PubMed:18729522, PubMed:20961038, PubMed:21254756, RESID:AA0551]
-comment: Cross-link 2.
-synonym: "(4Z)-4-[hydroxy(sulfanyl)methylidene]-2-[(2S)-pyrrolidin-2-yl]-1,3-oxazol-5(4H)-one [tautomer]" EXACT RESID-alternate []
-synonym: "5-hydroxy-2-[(2S)-pyrrolidin-2-yl]-1,3-oxazole-4-carbothioic O-acid" EXACT RESID-systematic []
-synonym: "CROSSLNK Proline 5-hydroxy-oxazole-4-carbothionic acid (Pro-Cys)" EXACT UniProt-feature []
-synonym: "L-proline 5-hydroxy-oxazole-4-carbothionic acid" EXACT RESID-name []
-property_value: DiffAvg "-4.03" xsd:float
-property_value: DiffFormula "C 0 H -4 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "-4.031300" xsd:float
-property_value: Formula "C 8 H 8 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "196.22" xsd:float
-property_value: MassMono "196.030649" xsd:float
-property_value: Origin "C, P" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0449
-is_a: MOD:02044
-is_a: MOD:02054
-is_a: MOD:01856
-
-[Term]
-id: MOD:01846
-name: methanobactin OB3b copper complex
-def: "A protein modification that effectively converts two L-cysteine residues, and a copper atom to the methanobactin OB3b copper complex." [PubMed:15361623, PubMed:18729522, PubMed:20961038, PubMed:21254756, RESID:AA0552]
-comment: Cross-link 2.
-synonym: "bis[4-(hydroxy[sulfanyl-kappaS]methylidene)-1,3-oxazol-5(4H)-onato-kappaN]copper" EXACT RESID-systematic []
-synonym: "METAL copper [Cu-methanobactin OB3b complex]" EXACT UniProt-feature []
-synonym: "methanobactin OB3b copper complex" EXACT RESID-name []
-property_value: DiffAvg "85.46" xsd:float
-property_value: DiffFormula "C 0 Cu 1 H -10 N 0 O 2 S 0" xsd:string
-property_value: DiffMono "84.841176" xsd:float
-property_value: Formula "C 6 Cu 1 H 0 N 2 O 4 S 2" xsd:string
-property_value: MassAvg "291.74" xsd:float
-property_value: MassMono "290.859546" xsd:float
-property_value: Origin "C, C" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00742
-is_a: MOD:02067
-
-[Term]
-id: MOD:01847
-name: L-cysteine sulfinyl phosphate
-def: "A protein modification that effectively converts an L-cysteine residue to L-cysteine sulfinyl phosphate." [PubMed:16565085, RESID:AA0557]
-synonym: "(2R)-2-amino-3-[(phosphonooxy)sulfinyl]propanoic acid" EXACT RESID-systematic []
-synonym: "cysteine sulfinic phosphoryl ester" EXACT RESID-alternate []
-synonym: "L-cysteine sulfinyl phosphate" EXACT RESID-name []
-property_value: DiffAvg "111.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 0 O 5 P 1 S 0" xsd:string
-property_value: DiffMono "111.956160" xsd:float
-property_value: Formula "C 3 H 6 N 1 O 6 P 1 S 1" xsd:string
-property_value: MassAvg "215.12" xsd:float
-property_value: MassMono "214.965345" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "hypothetical" xsd:string
-is_a: MOD:00708
-is_a: MOD:00861
-
-[Term]
-id: MOD:01848
-name: S-(spermidinoglutathion-S-yl)-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-(spermidinoglutathion-S-yl)-L-cysteine." [ChEBI:16613, PubMed:20530482, RESID:AA0558]
-synonym: "(2R)-2-amino-3-([(2R)-2-([(4S)-4-amino-4-carboxybutanoyl]amino)-2-([2-([3-([4-aminobutyl]amino)propyl]carbamoyl)methyl]carbamoyl)ethyl]disulfanyl)propanoic acid" EXACT RESID-systematic []
-synonym: "cysteine glutathionylspermidine disulfide" EXACT RESID-alternate []
-synonym: "L-gamma-glutamyl-[S-(L-cystein-S-yl)]-L-cysteinyl-N-{3-[(4-aminobutyl)amino]propyl}glycinamide" EXACT RESID-alternate []
-synonym: "S-(spermidinoglutathion-S-yl)-L-cysteine" EXACT RESID-name []
-property_value: DiffAvg "432.54" xsd:float
-property_value: DiffFormula "C 17 H 32 N 6 O 5 S 1" xsd:string
-property_value: DiffMono "432.215489" xsd:float
-property_value: Formula "C 20 H 37 N 7 O 6 S 2" xsd:string
-property_value: MassAvg "535.68" xsd:float
-property_value: MassMono "535.224674" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00905
-is_a: MOD:01862
-
-[Term]
-id: MOD:01849
-name: S-(2-aminovinyl)-D-cysteine (Cys-Cys)
-def: "A protein modification that effectively cross-links two L-cysteine residues by a thioether bond to form S-(2-aminovinyl)-D-cysteine." [PubMed:20805503, RESID:AA0204#CYS2]
-comment: Cross-link 2.
-synonym: "(2S)-2-amino-3-([(Z)-2-aminoethenyl]sulfanyl)propanoic acid" EXACT RESID-systematic []
-synonym: "(S,Z)-S-(2-aminovinyl)cysteine" EXACT RESID-alternate []
-synonym: "CROSSLNK S-(2-aminovinyl)-D-cysteine (Cys-Cys)" EXACT UniProt-feature []
-synonym: "S-(2-aminovinyl)-D-cysteine" EXACT RESID-name []
-property_value: DiffAvg "-80.10" xsd:float
-property_value: DiffFormula "C -1 H -4 N 0 O -2 S -1" xsd:string
-property_value: DiffMono "-79.993200" xsd:float
-property_value: Formula "C 5 H 7 N 2 O 1 S 1" xsd:string
-property_value: MassAvg "143.18" xsd:float
-property_value: MassMono "143.027909" xsd:float
-property_value: Origin "C, C" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-xref: uniprot.ptm:PTM-0446
-is_a: MOD:01850
-
-[Term]
-id: MOD:01850
-name: S-(2-aminovinyl)-D-cysteine
-def: "A protein modification that effectively cross-links either two L-cysteine residues, or an L-cysteine residue and an L-serine residue by a thioether bond to form S-(2-aminovinyl)-D-cysteine." [RESID:AA0204]
-comment: Cross-link 2.
-synonym: "(2S)-2-amino-3-([(Z)-2-aminoethenyl]sulfanyl)propanoic acid" EXACT RESID-systematic []
-synonym: "(S,Z)-S-(2-aminovinyl)cysteine" EXACT RESID-alternate []
-synonym: "S-(2-aminovinyl)-D-cysteine" EXACT RESID-name []
-property_value: Formula "C 5 H 7 N 2 O 1 S 1" xsd:string
-property_value: MassAvg "143.18" xsd:float
-property_value: MassMono "143.027909" xsd:float
-property_value: Origin "C, X" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-is_a: MOD:01851
-
-[Term]
-id: MOD:01851
-name: S-(2-aminovinyl)-cysteine
-def: "A protein modification that effectively cross-links either two L-cysteine residues, or an L-cysteine residue and an L-serine residue by a thioether bond to form S-(2-aminovinyl)-cysteine." [PubMed:18688235]
-comment: Cross-link 2.
-synonym: "2-amino-3-([2-aminoethenyl]sulfanyl)propanoic acid" EXACT PSI-MOD-alternate []
-property_value: Formula "C 5 H 7 N 2 O 1 S 1" xsd:string
-property_value: MassAvg "143.18" xsd:float
-property_value: MassMono "143.027909" xsd:float
-property_value: Origin "C, X" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-is_a: MOD:00687
-is_a: MOD:00859
-
-[Term]
-id: MOD:01852
-name: L-lysinoalanine (Lys-Cys)
-def: "A protein modification that effectively crosslinks an L-cysteine residue and an L-lysine residue to release hydrogen sulfide and form 2-amino-6-(2-amino-2-carboxyethylamino)hexanoic acid." [DeltaMass:0]
-comment: Cross-link 2. This entry is for a crosslink of peptidyl cysteine and peptidyl lysine. For the modification of peptidyl lysine by a free serine see MOD:01838. From DeltaMass: Average Mass: -34 with no citation or formula. [JSG]
-synonym: "Lysinoalanine (from Cysteine)" EXACT DeltaMass-label []
-property_value: DiffAvg "-34.08" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0 S -1" xsd:string
-property_value: DiffMono "-33.987721" xsd:float
-property_value: Formula "C 9 H 15 N 3 O 2" xsd:string
-property_value: MassAvg "197.24" xsd:float
-property_value: MassMono "197.116427" xsd:float
-property_value: Origin "C, K" xsd:string
-property_value: Source "hypothetical" xsd:string
-is_a: MOD:00692
-is_a: MOD:02044
-is_a: MOD:02051
-is_a: MOD:01853
-
-[Term]
-id: MOD:01853
-name: L-lysinoalanine
-def: "A protein modification that effectively converts an L-lysine residue to L-lysinoalanine either by forming a cross-link with peptidyl-cysteine or peptidyl-serine, or by condensation with free serine." [PubMed:18688235]
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00859
-is_a: MOD:00912
-
-[Term]
-id: MOD:01854
-name: sulfur monooxygenated residue
-def: "A protein modification that effectively adds one oxygen atom to a sulfur atom of a residue without removing hydrogen atoms." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:00680
-
-[Term]
-id: MOD:01855
-name: sulfur dioxygenated residue
-def: "A protein modification that effectively adds two oxygen atoms to a sulfur atom of a residue without removing hydrogen atoms." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:00680
-
-[Term]
-id: MOD:01856
-name: oxazole/oxazoline ring crosslinked residues (Cys)
-def: "A protein modification that crosslinks two residues by rearrangement and condensation of a cysteine with the carbonyl of the preceding residue to form a 1,3-oxazole-4-carbothionic acid." [PubMed:18688235]
-is_a: MOD:01419
-
-[Term]
-id: MOD:01857
-name: 2-(L-cystein-S-yl)-methionine
-def: "A protein modification that effectively cross-links an L-cysteine residue and an L-methionine residue by a thioether bond to form 2-(L-cystein-S-yl)-methionine." [PubMed:20805502, RESID:AA0559]
-comment: Cross-link 2. The chirality around the methionine alpha-carbon has not been determined.
-synonym: "(2R)-2-amino-2-([2-amino-2-carboxyethyl]sulfanyl)-4-(methylsulfanyl)butanoic acid" EXACT RESID-systematic []
-synonym: "2-(L-cystein-S-yl)-methionine" EXACT RESID-name []
-synonym: "CROSSLNK 2-(S-cysteinyl)-methionine (Cys-Met)" EXACT UniProt-feature []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 8 H 12 N 2 O 2 S 2" xsd:string
-property_value: MassAvg "232.32" xsd:float
-property_value: MassMono "232.034020" xsd:float
-property_value: Origin "C, M" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0495
-is_a: MOD:02044
-is_a: MOD:02052
-is_a: MOD:01992
-
-[Term]
-id: MOD:01858
-name: S-(N-acetylamino)glucosyl-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-(N-acetylamino)glucosyl-L-cysteine." [ChEBI:61631, PubMed:21251913, PubMed:21395300, RESID:AA0560]
-synonym: "(2R)-2-amino-3-(2-acetamido-2-deoxy-beta-D-glucopyranosylsulfanyl)propanoic acid" EXACT RESID-systematic []
-synonym: "CARBOHYD S-linked (GlcNAc) cysteine" EXACT UniProt-feature []
-synonym: "S-(N-acetylamino)glucosyl-L-cysteine" EXACT RESID-name []
-synonym: "S-[(N-acetylamino)glycosyl]cysteine" EXACT RESID-alternate []
-synonym: "S-[beta-D-(N-acetylamino)glucopyranosyl]cysteine" EXACT RESID-alternate []
-property_value: DiffAvg "203.19" xsd:float
-property_value: DiffFormula "C 8 H 13 N 1 O 5 S 0" xsd:string
-property_value: DiffMono "203.079373" xsd:float
-property_value: Formula "C 11 H 18 N 2 O 6 S 1" xsd:string
-property_value: MassAvg "306.33" xsd:float
-property_value: MassMono "306.088557" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0628
-is_a: MOD:00426
-is_a: MOD:00448
-is_a: MOD:00905
-
-[Term]
-id: MOD:01859
-name: 4-amino-3-isothiazolidinone-L-phenylalanine
-def: "A protein modification that effectively crosslinks an L-cysteine residue and an L-phenylalanine residue to form 4-amino-3-isothiazolidinone-L-phenylalanine." [PubMed:17502599, RESID:AA0562]
-comment: Cross-link 2.
-synonym: "(2S)-2-[(4R)-4-amino-3-oxo-1,2-thiazolidin-2-yl]-3-phenylpropanoic acid" EXACT RESID-systematic []
-synonym: "2-(4-amino-3-oxo-isothiazolidin-2-yl)-3-phenylpropanoic acid" EXACT RESID-alternate []
-synonym: "4-amino-3-isothiazolidinone-L-phenylalanine" EXACT RESID-alternate []
-synonym: "CROSSLNK N,N-(cysteine-1,S-diyl)phenylalanine (Cys-Phe)" EXACT UniProt-feature []
-synonym: "cysteinyl phenylalanine sulfenamide" EXACT RESID-alternate []
-synonym: "N,N-(L-cysteine-1,S-diyl)-L-phenylalanine" EXACT RESID-name []
-synonym: "phenylalanine-cysteine sulfenyl amide cross-link" EXACT RESID-alternate []
-synonym: "phenylalanine-cysteine sulphenyl amide cross-link" EXACT RESID-alternate []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 12 H 12 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "248.30" xsd:float
-property_value: MassMono "248.061949" xsd:float
-property_value: Origin "C, F" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: uniprot.ptm:PTM-0451
-is_a: MOD:02044
-is_a: MOD:02053
-is_a: MOD:01861
-
-[Term]
-id: MOD:01860
-name: L-cysteine bacillithiol disulfide
-def: "A protein modification that effectively converts an L-cysteine residue to L-cysteine bacillithiol disulfide." [ChEBI:61338, PubMed:19578333, RESID:AA0563]
-synonym: "(2S)-(2-[S-(L-cystein-S-yl)-L-cysteinyl]amino-2-deoxy-alpha-D-glucopyranosyloxy)-butanedioic acid" EXACT RESID-systematic []
-synonym: "BSH" EXACT RESID-alternate []
-synonym: "L-cysteine bacillithiol disulfide" EXACT RESID-name []
-synonym: "MOD_RES S-bacillithiol cysteine disulfide" EXACT UniProt-feature []
-property_value: DiffAvg "396.37" xsd:float
-property_value: DiffFormula "C 13 H 20 N 2 O 10 S 1" xsd:string
-property_value: DiffMono "396.083866" xsd:float
-property_value: Formula "C 16 H 25 N 3 O 11 S 2" xsd:string
-property_value: MassAvg "499.51" xsd:float
-property_value: MassMono "499.093051" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0452
-is_a: MOD:00905
-is_a: MOD:01862
-
-[Term]
-id: MOD:01861
-name: isothiazolidinone ring crosslinked residues
-def: "A protein modification that crosslinks two residues by condensation of a cysteine thiol with the amido nitrogen of the following residue to form an isothiazolidinone ring." [PubMed:18688235]
-comment: The isothiazolidinone ring is usually formed by the reaction of a cysteine sulfenic acid with the amido nitrogen releasing water.
-is_a: MOD:00033
-
-[Term]
-id: MOD:01862
-name: disulfide conjugated residue
-def: "A protein modification that effectively replaces the hydrogen atom of a cysteine sulfanyl group with a substituted sulfanyl group, forming a disulfide bond that does not cross-link two encoded peptide chains." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "S-thiolation" EXACT PSI-MOD-alternate []
-property_value: Origin "C" xsd:string
-is_a: MOD:01886
-
-[Term]
-id: MOD:01863
-name: mTRAQ reporter+balance reagent acylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of a residue with one of the Applied Biosystems mTRAQ reagent reporter+balance groups." [PubMed:18688235]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Applied Biosystems mTRAQ(TM) reagent" RELATED Unimod-alternate []
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01426
-is_a: MOD:01705
-
-[Term]
-id: MOD:01864
-name: mTRAQ light reporter+balance reagent acylated residue
-def: "A protein modification that effectively replaces a hydrogen atom of a residue with the Applied Biosystems mTRAQ light reporter+balance group." [Unimod:888]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Applied Biosystems mTRAQ(TM) reagent" RELATED Unimod-alternate []
-synonym: "mTRAQ heavy" RELATED Unimod-description []
-property_value: DiffAvg "140.09" xsd:float
-property_value: DiffFormula "(12)C 7 H 12 (14)N 2 (16)O 1" xsd:string
-property_value: DiffMono "140.094963" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:888
-is_a: MOD:01863
-is_a: MOD:01868
-
-[Term]
-id: MOD:01865
-name: mTRAQ light reporter+balance reagent acylated N-terminal
-def: "A protein modification that effectively replaces a hydrogen atom of a protein N-terminal with the Applied Biosystems mTRAQ light reporter+balance group." [OMSSA:208, Unimod:888#N-term]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Applied Biosystems mTRAQ(TM) reagent" RELATED Unimod-alternate []
-synonym: "mTRAQ light" RELATED Unimod-description []
-synonym: "mTRAQ light on nterm" EXACT OMSSA-label []
-property_value: DiffAvg "140.09" xsd:float
-property_value: DiffFormula "(12)C 7 H 12 (14)N 2 (16)O 1" xsd:string
-property_value: DiffMono "140.094963" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:888
-is_a: MOD:01864
-
-[Term]
-id: MOD:01866
-name: mTRAQ light reporter+balance reagent N6-acylated lysine
-def: "A protein modification that effectively replaces the N6-amino hydrogen atom of a lysine residue with the Applied Biosystems mTRAQ light reporter+balance group." [OMSSA:209, Unimod:888#K]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Applied Biosystems mTRAQ(TM) reagent" RELATED Unimod-alternate []
-synonym: "mTRAQ light" RELATED Unimod-description []
-synonym: "mTRAQ light on K" EXACT OMSSA-label []
-property_value: DiffAvg "140.09" xsd:float
-property_value: DiffFormula "(12)C 7 H 12 (14)N 2 (16)O 1" xsd:string
-property_value: DiffMono "140.094963" xsd:float
-property_value: Formula "(12)C 13 H 24 N 2 (14)N 2 O 1 (16)O 1" xsd:string
-property_value: MassAvg "268.19" xsd:float
-property_value: MassMono "268.189926" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:888
-is_a: MOD:01864
-is_a: MOD:01875
-
-[Term]
-id: MOD:01867
-name: mTRAQ light reporter+balance reagent O4'-acylated tyrosine
-def: "A protein modification that effectively replaces the O4'-hydrogen atom of a tyrosine residue with the Applied Biosystems mTRAQ light reporter+balance group." [OMSSA:210, Unimod:888#Y]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification.
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "Applied Biosystems mTRAQ(TM) reagent" RELATED Unimod-alternate []
-synonym: "mTRAQ light" RELATED Unimod-description []
-synonym: "mTRAQ light on Y" EXACT OMSSA-label []
-property_value: DiffAvg "140.09" xsd:float
-property_value: DiffFormula "(12)C 7 H 12 (14)N 2 (16)O 1" xsd:string
-property_value: DiffMono "140.094963" xsd:float
-property_value: Formula "(12)C 16 H 21 (14)N 3 O 2 (16)O 1" xsd:string
-property_value: MassAvg "303.16" xsd:float
-property_value: MassMono "303.158292" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:888
-is_a: MOD:00919
-is_a: MOD:01864
-
-[Term]
-id: MOD:01868
-name: modifications with monoisotopic mass differences that are nominally equal at 140.094963 Da
-def: "Modifications that have monoisotopic mass differences from their respective origins of 140.094963 Da." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:01515
-
-[Term]
-id: MOD:01869
-name: mTRAQ light reporter fragment
-def: "The protein modification reporter fragment produced by an Applied Biosystems mTRAQ light reagent derivatized residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "4-methyl-1-methylidenepiperazin-1-ium" EXACT PSI-MOD-alternate []
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "(12)C 6 H 13 (14)N 2" xsd:string
-property_value: MassAvg "113.11" xsd:float
-property_value: MassMono "113.107325" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01870
-relationship: derives_from MOD:01864
-
-[Term]
-id: MOD:01870
-name: mTRAQ reporter fragment
-def: "A protein modification reporter fragment produced by an Applied Biosystems mTRAQ reagent derivatized residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-is_a: MOD:01520
-
-[Term]
-id: MOD:01871
-name: cyclized N-terminal S-carboxamidomethyl-L-cysteine
-def: "A protein modification that effectively cyclizes an S-carboxamidomethyl-L-cysteine residue to (R)-5-oxo-1,4-tetrahydrothiazine-3-carboxylic acid with the loss of ammonia." [DeltaMass:336, PubMed:12643538, Unimod:26]
-subset: PSI-MOD-slim
-synonym: "(R)-5-oxoperhydro-1,4-thiazine-3-carboxylic acid" EXACT DeltaMass-label []
-synonym: "5-oxothiomorpholine-3-carboxylic acid" EXACT PSI-MOD-alternate []
-synonym: "Otc" EXACT DeltaMass-label []
-synonym: "Pyro-carbamidomethyl" RELATED Unimod-interim []
-synonym: "S-carbamoylmethylcysteine cyclization (N-terminus)" RELATED Unimod-description []
-property_value: DiffAvg "-17.03" xsd:float
-property_value: DiffFormula "C 0 H -3 N -1 O 0 S 0" xsd:string
-property_value: DiffMono "-17.026549" xsd:float
-property_value: Formula "C 5 H 6 N 1 O 2 S 1" xsd:string
-property_value: MassAvg "144.17" xsd:float
-property_value: MassMono "144.011924" xsd:float
-property_value: Origin "MOD:01060" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:26
-is_a: MOD:01160
-relationship: contains MOD:00419
-relationship: derives_from MOD:01060
-
-[Term]
-id: MOD:01872
-name: cyclized N-terminal S-carboxymethyl-L-cysteine
-def: "A protein modification that effectively cyclizes an S-carboxymethyl-L-cysteine residue to (R)-5-oxo-1,4-tetrahydrothiazine-3-carboxylic acid with the loss of water." [PubMed:12643538, Unimod:26]
-comment: Contrary to the impression given in Unimod entry 26, the cyclization of N-terminal S-carboxymethyl-L-cysteine is not reported in PubMed:1263538. The cyclization would be expected to proceed under strongly acidic conditions [JSG].
-subset: PSI-MOD-slim
-synonym: "(R)-5-oxoperhydro-1,4-thiazine-3-carboxylic acid" EXACT DeltaMass-label []
-synonym: "5-oxothiomorpholine-3-carboxylic acid" EXACT PSI-MOD-alternate []
-synonym: "Otc" EXACT DeltaMass-label []
-synonym: "Pyro-carbamidomethyl" RELATED Unimod-interim []
-synonym: "S-carbamoylmethylcysteine cyclization (N-terminus)" RELATED Unimod-description []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 5 H 6 N 1 O 2 S 1" xsd:string
-property_value: MassAvg "144.17" xsd:float
-property_value: MassMono "144.011924" xsd:float
-property_value: Origin "MOD:01061" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:26
-is_a: MOD:00704
-relationship: contains MOD:00419
-relationship: derives_from MOD:01061
-
-[Term]
-id: MOD:01873
-name: N-carboxy-L-alanine
-def: "A protein modification that effectively converts an L-alanine residue to N-carboxy-L-alanine." [PubMed:18688235, PubMed:4593770, PubMed:4647257, PubMed:8312270]
-comment: This metastable modification can be formed by a protein N-terminal in solutions with a high concentration of dissolved carbon dioxide [JSG].
-synonym: "(S)-2-carboxyamino-propanoic acid" EXACT PSI-MOD-alternate []
-synonym: "2-carbamic-propanoic acid" EXACT PSI-MOD-alternate []
-synonym: "N-carboxymethionine" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "44.01" xsd:float
-property_value: DiffFormula "C 1 H 0 N 0 O 2" xsd:string
-property_value: DiffMono "43.989829" xsd:float
-property_value: Formula "C 4 H 6 N 1 O 3" xsd:string
-property_value: MassAvg "116.10" xsd:float
-property_value: MassMono "116.034768" xsd:float
-property_value: Origin "A" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00901
-is_a: MOD:01152
-
-[Term]
-id: MOD:01874
-name: N-carboxy-L-valine
-def: "A protein modification that effectively converts an L-alanine residue to N-carboxy-L-valine." [PubMed:18688235, PubMed:4593770, PubMed:4647257, PubMed:8312270]
-comment: This metastable modification can be formed by a protein N-terminal in solutions with a high concentration of dissolved carbon dioxide [JSG].
-synonym: "(S)-2-carboxyamino-propanoic acid" EXACT PSI-MOD-alternate []
-synonym: "2-carbamic-propanoic acid" EXACT PSI-MOD-alternate []
-synonym: "N-carboxymethionine" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "44.01" xsd:float
-property_value: DiffFormula "C 1 H 0 N 0 O 2" xsd:string
-property_value: DiffMono "43.989829" xsd:float
-property_value: Formula "C 6 H 10 N 1 O 3" xsd:string
-property_value: MassAvg "144.15" xsd:float
-property_value: MassMono "144.066068" xsd:float
-property_value: Origin "V" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00920
-is_a: MOD:01152
-
-[Term]
-id: MOD:01875
-name: N6-acylated L-lysine
-def: "A protein modification that effectively replaces an N6-amino hydrogen atom of L-lysine with an acyl group." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "N6AcylLys" EXACT PSI-MOD-label []
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00670
-is_a: MOD:00912
-
-[Term]
-id: MOD:01876
-name: 4x(1)H,4x(12)C-labeled alpha-amino succinylated residue
-def: "OBSOLETE because identical to MOD:00457" [PubMed:18688235]
-property_value: DiffAvg "100.02" xsd:float
-property_value: DiffFormula "(12)C 4 (1)H 4 O 3" xsd:string
-property_value: DiffMono "100.016044" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-replaced_by: MOD:00457
-is_obsolete: true
-
-[Term]
-id: MOD:01877
-name: 2-(4-guanidinobutanoyl)-5-hydroxyimidazole-4-carbothionic acid
-def: "A protein modification that effectively converts an L-cysteine residue and an L-arginine residue to 2-(4-guanidinobutanoyl)-5-hydroxyimidazole-4-carbothionic acid." [PubMed:20961038, RESID:AA0553]
-comment: Cross-link 2.
-synonym: "(4Z)-2-(4-guanidinobutanoyl)-5-oxo-4-(sulfanylmethylidene)-4,5-dihydro-1H-imidazole" EXACT RESID-alternate []
-synonym: "2-(4-guanidinobutanoyl)-5-hydroxy-1H-imidazole-4-carbothioic O-acid" EXACT RESID-systematic []
-synonym: "2-(4-guanidinobutanoyl)-5-hydroxy-4-thioformyl-1H-imidazole [tautomer]" EXACT RESID-alternate []
-synonym: "2-(4-guanidinobutanoyl)-5-hydroxyimidazole-4-carbothionic acid" EXACT RESID-name []
-synonym: "CROSSLNK 2-(4-guanidinobutanoyl)-5-hydroxyimidazole-4-carbothionic acid (Arg-Cys)" EXACT UniProt-feature []
-property_value: DiffAvg "-6.05" xsd:float
-property_value: DiffFormula "C 0 H -6 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "-6.046950" xsd:float
-property_value: Formula "C 9 H 12 N 5 O 2 S 1" xsd:string
-property_value: MassAvg "254.29" xsd:float
-property_value: MassMono "254.071171" xsd:float
-property_value: Origin "C, R" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0457
-is_a: MOD:02041
-is_a: MOD:02044
-is_a: MOD:01883
-
-[Term]
-id: MOD:01878
-name: L-threonine 5-hydroxyoxazole-4-carbonthionic acid
-def: "A protein modification that effectively converts an L-cysteine residue and an L-threonine residue to L-threonine 5-hydroxyoxazole-4-carbothionic acid." [PubMed:20961038, RESID:AA0554]
-comment: Cross-link 2.
-synonym: "(4Z)-2-[(1S,2R)-1-amino-2-hydroxypropyl]-4-(sulfanylmethylidene)-1,3-oxazol-5(4H)-one [tautomer]" EXACT RESID-alternate []
-synonym: "2-[(1S,2R)-1-amino-2-hydroxypropyl]-5-hydroxy-1,3-oxazole-4-carbothioic O-acid" EXACT RESID-systematic []
-synonym: "CROSSLNK Threonine 5-hydroxy-oxazole-4-carbonthionic acid (Thr-Cys)" EXACT UniProt-feature []
-synonym: "L-threonine 5-hydroxy-oxazole-4-carbonthionic acid" EXACT RESID-name []
-property_value: DiffAvg "-4.03" xsd:float
-property_value: DiffFormula "C 0 H -4 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "-4.031300" xsd:float
-property_value: Formula "C 7 H 8 N 2 O 3 S 1" xsd:string
-property_value: MassAvg "200.21" xsd:float
-property_value: MassMono "200.025563" xsd:float
-property_value: Origin "C, T" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0458
-is_a: MOD:02044
-is_a: MOD:02056
-is_a: MOD:01856
-
-[Term]
-id: MOD:01879
-name: methanobactin SB2 copper complex
-def: "A protein modification that effectively converts two L-cysteine residues, an L-arginine residue, an L-threonine residue and a copper atom to the methanobactin SB2 copper complex." [PubMed:20961038, RESID:AA0555]
-comment: Cross-link 2.
-synonym: "[5-(hydroxy[sulfanyl-kappaS]methylene)-3,5-dihydro-4H-imidazol-4-onato-kappaN1][4-(hydroxy[sulfanyl-kappaS]methylene)-1,3-oxazol-5(4H)-onato-kappaN]copper" EXACT RESID-systematic []
-synonym: "METAL copper [Cu-methanobactin SB2 complex]" EXACT UniProt-feature []
-synonym: "methanobactin SB2 copper complex" EXACT RESID-name []
-property_value: DiffAvg "84.48" xsd:float
-property_value: DiffFormula "C 0 Cu 1 H -9 N 1 O 1 S 0" xsd:string
-property_value: DiffMono "83.857161" xsd:float
-property_value: Formula "C 6 Cu 1 H 1 N 3 O 3 S 2" xsd:string
-property_value: MassAvg "290.76" xsd:float
-property_value: MassMono "289.875530" xsd:float
-property_value: Origin "C, C, R, T" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00742
-is_a: MOD:02067
-
-[Term]
-id: MOD:01880
-name: L-deoxyhypusine
-def: "modification from RESID" [ChEBI:50038, PubMed:16452303, RESID:AA0564]
-synonym: "(2S)-2-amino-6-[(4-aminobutyl)amino]hexanoic acid" EXACT RESID-systematic []
-synonym: "deoxyhypusine" EXACT RESID-alternate []
-synonym: "L-deoxyhypusine" EXACT RESID-name []
-synonym: "N6-(4-aminobutyl)lysine" EXACT RESID-alternate []
-synonym: "MOD_RES Deoxyhypusine" EXACT UniProt-feature []
-property_value: DiffAvg "71.12" xsd:float
-property_value: DiffFormula "C 4 H 9 N 1 O 0" xsd:string
-property_value: DiffMono "71.073499" xsd:float
-property_value: Formula "C 10 H 21 N 3 O 1" xsd:string
-property_value: MassAvg "199.30" xsd:float
-property_value: MassMono "199.168462" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0684
-is_a: MOD:00912
-is_a: MOD:01884
-
-[Term]
-id: MOD:01881
-name: 3-(L-phenylalan-2'-yl)-L-valine
-def: "A protein modification that effectively crosslinks an L-phenylalanine residue and an L-valine residue by a free radical process effectively releasing a hydrogen molecule and forming 3-(L-phenylalan-2'-yl)-L-valine." [PubMed:21596985, RESID:AA0565]
-comment: Cross-link 2.
-synonym: "(2S)-2-amino-4-(2-[(2S)-2-amino-2-carboxyethyl]phenyl)-3-methylbutanoic acid" EXACT RESID-systematic []
-synonym: "3-(L-phenylalan-2'-yl)-L-valine" EXACT RESID-name []
-synonym: "symerythrin valine-phenylalanine cross-link" EXACT RESID-alternate []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 14 H 16 N 2 O 2" xsd:string
-property_value: MassAvg "244.29" xsd:float
-property_value: MassMono "244.121178" xsd:float
-property_value: Origin "F, V" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00692
-is_a: MOD:02053
-is_a: MOD:02059
-
-[Term]
-id: MOD:01882
-name: 5-imidazolinone ring crosslinked residues (Gly)
-def: "A protein modification that effectively crosslinks the carbonyl of an amino acid residue at position n with the alpha amino of a glycine residue at position n+2 to form a 5-imidazolinone ring." [PubMed:18688235]
-is_a: MOD:00691
-
-[Term]
-id: MOD:01883
-name: 5-imidazolinone ring crosslinked residues (Cys)
-def: "A protein modification that crosslinks two residues by rearrangement and condensation of a cysteine with the carbonyl of the preceding residue to form a 5-imidazolinone ring." [PubMed:18688235]
-is_a: MOD:00691
-
-[Term]
-id: MOD:01884
-name: 4-aminobutylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with a 4-aminobutyl group, usually derived from spermidine." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: Origin "X" xsd:string
-is_a: MOD:00001
-
-[Term]
-id: MOD:01885
-name: biotinylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with a biotinyl group." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "5-((3aS,4S,6aR)-hexahydro-2-oxo-1H-thieno[3,4-d]imidazol-4-yl)-1-oxopentyl" EXACT PSI-MOD-alternate []
-synonym: "Biotinylation" EXACT PSI-MOD-alternate []
-synonym: "BtnRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "226.29" xsd:float
-property_value: DiffFormula "C 10 H 14 N 2 O 2 S 1" xsd:string
-property_value: DiffMono "226.077599" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00649
-
-[Term]
-id: MOD:01886
-name: thiolated residue
-def: "A protein modification that effectively replaces a hydrogen atom with an sulfanyl or substituted sulfanyl group." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: Origin "X" xsd:string
-is_a: MOD:00860
-
-[Term]
-id: MOD:01887
-name: Uniblue A derivatized lysine
-def: "A protein modification that is produced by reaction with 1-amino-4-{[3-(ethenylsulfonyl)phenyl]amino}-9,10-dioxo-9,10-dihydroanthracene-2-sulfonate, Uniblue A, to form Uniblue A lysine adduct." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "1-amino-4-{[3-(ethenylsulfonyl)phenyl]amino}-9,10-dioxo-9,10-dihydroanthracene-2-sulfonate" EXACT PSI-MOD-alternate []
-synonym: "1-amino-9,10-dioxo-4-{[3-(vinylsulfonyl)phenyl]amino}-9,10-dihydroanthracene-2-sulfonate" EXACT PSI-MOD-alternate []
-synonym: "N6UniblueALys" EXACT PSI-MOD-label []
-synonym: "Uniblue A" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "484.50" xsd:float
-property_value: DiffFormula "C 22 H 16 N 2 O 7 S 2" xsd:string
-property_value: DiffMono "484.039893" xsd:float
-property_value: Formula "C 28 H 28 N 4 O 8 S 2" xsd:string
-property_value: MassAvg "612.67" xsd:float
-property_value: MassMono "612.134856" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00912
-is_a: MOD:01659
-
-[Term]
-id: MOD:01888
-name: didehydrogenated residue
-def: "A protein modification that effectively removes two neutral hydrogen atoms (proton and electron) from a residue." [Unimod:401]
-subset: PSI-MOD-slim
-synonym: "2dHRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Origin "X" xsd:string
-xref: Unimod:401
-is_a: MOD:00683
-
-[Term]
-id: MOD:01889
-name: S-(2-succinyl)-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-(2-succinyl)-L-cysteine, by addition of either fumaric acid or maleic acid." [PubMed:16624247, PubMed:18448829, PubMed:20677745, RESID:AA0561, Unimod:957]
-synonym: "(2R)-2-amino-3-([(1R)-1,2-dicarboxyethyl]sulfanyl)propanoic acid" EXACT RESID-systematic []
-synonym: "(2R)-2-{[(2R)-2-amino-2-carboxyethyl]sulfanyl}butanedioic acid" EXACT RESID-alternate []
-synonym: "2-((2-amino-2-carboxyethyl)thio)butanedioic acid" EXACT RESID-alternate []
-synonym: "2-amino-3-(1,2-dicarboxyethylthio)propanoic acid" EXACT RESID-alternate []
-synonym: "S-(1,2-dicarboxyethyl)cysteine" EXACT RESID-alternate []
-synonym: "S-(2-succinyl)-L-cysteine" EXACT RESID-name []
-synonym: "S-(2-succinyl)cysteine" EXACT RESID-alternate []
-synonym: "S-[(2R)-2-succinyl]-L-cysteine" EXACT RESID-alternate []
-synonym: "MOD_RES S-(2-succinyl)cysteine" EXACT UniProt-feature []
-property_value: DiffAvg "116.07" xsd:float
-property_value: DiffFormula "C 4 H 4 N 0 O 4 S 0" xsd:string
-property_value: DiffMono "116.010959" xsd:float
-property_value: Formula "C 7 H 9 N 1 O 5 S 1" xsd:string
-property_value: MassAvg "219.21" xsd:float
-property_value: MassMono "219.020143" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:957
-xref: uniprot.ptm:PTM-0674
-is_a: MOD:00001
-is_a: MOD:00905
-
-[Term]
-id: MOD:01890
-name: N-[(L-histidin-1'-yl)methyl]-L-methionine (fMet)
-def: "A protein modification that effectively crosslinks an N-formyl-L-methionine residue and an L-histidine residue to form N-[(L-histidin-1'-yl)methyl]-L-methionine." [PubMed:19622680, RESID:AA0566#FMET]
-comment: Cross-link 2.
-synonym: "(2S)-2-([(4-[(2S)-2-amino-2-carboxyethyl]-1H-imidazol-1-yl)methyl]amino)-4-(methylsulfanyl)butanoic acid" EXACT RESID-systematic []
-synonym: "N-[(L-histidin-1'-yl)methyl]-L-methionine" EXACT RESID-name []
-property_value: DiffAvg "-16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-15.994915" xsd:float
-property_value: Formula "C 12 H 17 N 4 O 2 S 1" xsd:string
-property_value: MassAvg "281.35" xsd:float
-property_value: MassMono "281.107222" xsd:float
-property_value: Origin "H, MOD:00030" xsd:string
-property_value: Source "hypothetical" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:02048
-is_a: MOD:02062
-
-[Term]
-id: MOD:01891
-name: N-[(L-histidin-1'-yl)methyl]-L-methionine (Met)
-def: "A protein modification that effectively crosslinks an L-methionine residue and an L-histidine residue to form N-[(L-histidin-1'-yl)methyl]-L-methionine." [PubMed:19622680, RESID:AA0566#MET]
-comment: Cross-link 2.
-synonym: "(2S)-2-([(4-[(2S)-2-amino-2-carboxyethyl]-1H-imidazol-1-yl)methyl]amino)-4-(methylsulfanyl)butanoic acid" EXACT RESID-systematic []
-synonym: "N-[(L-histidin-1'-yl)methyl]-L-methionine" EXACT RESID-name []
-property_value: DiffAvg "12.01" xsd:float
-property_value: DiffFormula "C 1 H 0 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "12.000000" xsd:float
-property_value: Formula "C 12 H 17 N 4 O 2 S 1" xsd:string
-property_value: MassAvg "281.35" xsd:float
-property_value: MassMono "281.107222" xsd:float
-property_value: Origin "H, M" xsd:string
-property_value: Source "hypothetical" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:02048
-is_a: MOD:02052
-
-[Term]
-id: MOD:01892
-name: N6-crotonyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-crotonyl-L-lysine." [PubMed:21925322, RESID:AA0567]
-synonym: "(2S)-2-amino-6-[(2E)-but-2-enamido]hexanoic acid" EXACT RESID-alternate []
-synonym: "(2S)-2-amino-6-[(2E)-but-2-enoylamino]hexanoic acid" EXACT RESID-systematic []
-synonym: "(2S)-2-azanyl-6-[(2E)-but-2-enoylazanyl]hexanoic acid" EXACT RESID-alternate []
-synonym: "MOD_RES N6-crotonyl-L-lysine" EXACT UniProt-feature []
-synonym: "N(epsilon)-crotonyllysine" EXACT RESID-alternate []
-synonym: "N6-(E)-crotonyllysine" EXACT RESID-alternate []
-synonym: "N6-[(2E)-2-butenoyl]-L-lysine" EXACT RESID-alternate []
-synonym: "N6-crotonyl-L-lysine" EXACT RESID-name []
-synonym: "N6-crotonyllysine" EXACT RESID-alternate []
-synonym: "N6-trans-crotonyllysine" EXACT RESID-alternate []
-property_value: DiffAvg "68.07" xsd:float
-property_value: DiffFormula "C 4 H 4 N 0 O 1" xsd:string
-property_value: DiffMono "68.026215" xsd:float
-property_value: Formula "C 10 H 16 N 2 O 2" xsd:string
-property_value: MassAvg "196.25" xsd:float
-property_value: MassMono "196.121178" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: uniprot.ptm:PTM-0475
-is_a: MOD:01875
-
-[Term]
-id: MOD:01893
-name: N6-malonyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-malonyl-L-lysine." [PubMed:21908771, PubMed:8349414, RESID:AA0568]
-synonym: "(2S)-2-amino-6-[(carboxyacetyl)amino]hexanoic acid" EXACT RESID-systematic []
-synonym: "2-azanyl-6-[(carboxyacetyl)azanyl]hexanoic acid" EXACT RESID-alternate []
-synonym: "malonyllysine" EXACT RESID-alternate []
-synonym: "MOD_RES N6-malonyllysine" EXACT UniProt-feature []
-synonym: "N(epsilon)-(malonyl)lysine" EXACT RESID-alternate []
-synonym: "N6-(carboxyacetyl)lysine" EXACT RESID-alternate []
-synonym: "N6-malonyl-L-lysine" EXACT RESID-name []
-synonym: "N6-malonyllysine" EXACT RESID-alternate []
-property_value: DiffAvg "86.05" xsd:float
-property_value: DiffFormula "C 3 H 2 N 0 O 3" xsd:string
-property_value: DiffMono "86.000394" xsd:float
-property_value: Formula "C 9 H 14 N 2 O 4" xsd:string
-property_value: MassAvg "214.22" xsd:float
-property_value: MassMono "214.095357" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: uniprot.ptm:PTM-0467
-is_a: MOD:01875
-
-[Term]
-id: MOD:01894
-name: propanoylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with an propanoyl group." [PubMed:11857757, PubMed:11999733, PubMed:12175151, Unimod:58]
-synonym: "Propionate labeling reagent light form (N-term & K)" RELATED Unimod-description []
-synonym: "Propionyl" RELATED PSI-MS-label []
-property_value: DiffAvg "56.06" xsd:float
-property_value: DiffFormula "C 3 H 4 O 1" xsd:string
-property_value: DiffMono "56.026215" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:58
-is_a: MOD:00649
-
-[Term]
-id: MOD:01895
-name: alpha-amino 3x(12)C-labeled propanoylated residue
-def: "A protein modification that effectively replaces a residue alpha-amino- or alpha-imino-hydrogen with a 3x(12)C-labeled propanoyl group." [PubMed:11857757, PubMed:11999733, PubMed:12175151, Unimod:58#N-term]
-synonym: "Propionate labeling reagent light form (N-term & K)" RELATED Unimod-description []
-synonym: "Propionyl" RELATED PSI-MS-label []
-property_value: DiffAvg "56.03" xsd:float
-property_value: DiffFormula "(12)C 3 H 4 O 1" xsd:string
-property_value: DiffMono "56.026215" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:58
-relationship: derives_from MOD:00451
-is_a: MOD:01426
-
-[Term]
-id: MOD:01896
-name: trifluoroacetic acid adduct
-def: "A protein modification produced by trifluoroacetic acid forming an adduct, either a salt or a hydrogen bonded carboxylic acid dimer, with an amino acid residue." [PubMed:18688235]
-comment: Trifluoroacetic acid has been observed to form adducts in both negative and positive mode analysis (Mark Collins, private communication) [JSG].
-synonym: "TFA" EXACT DeltaMass-label []
-property_value: DiffAvg "114.02" xsd:float
-property_value: DiffFormula "C 2 F 3 H 1 O 2" xsd:string
-property_value: DiffMono "113.992864" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00498
-is_a: MOD:00848
-
-[Term]
-id: MOD:01897
-name: 5-hydroxy-3-methyl-L-proline (Ile)
-def: "A protein modification that effectively converts an L-isoleucine residue to 5-hydroxy-3-methyl-L-proline." [PubMed:21788474, PubMed:7592021, PubMed:8557573, RESID:AA0473]
-synonym: "(2S,3S,5Xi)-5-hydroxy-3-methylpyrrolidine-2-carboxylic acid" EXACT RESID-systematic []
-synonym: "5-hydroxy-3-methyl-L-proline" EXACT RESID-name []
-synonym: "5-hydroxy-3-methylproline" EXACT RESID-alternate []
-synonym: "5Hy3MePro(Ile)" EXACT PSI-MOD-label []
-synonym: "beta-methyl-delta-hydroxyproline" EXACT RESID-alternate []
-synonym: "MOD_RES 5-hydroxy-3-methylproline (Ile)" EXACT UniProt-feature []
-property_value: DiffAvg "13.98" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 1" xsd:string
-property_value: DiffMono "13.979265" xsd:float
-property_value: Formula "C 6 H 9 N 1 O 2" xsd:string
-property_value: MassAvg "127.14" xsd:float
-property_value: MassMono "127.063329" xsd:float
-property_value: Origin "I" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0466
-is_a: MOD:00601
-is_a: MOD:00679
-is_a: MOD:00910
-is_a: MOD:01905
-
-[Term]
-id: MOD:01898
-name: N2,N2-dimethyl-L-arginine
-def: "modification from RESID" [PubMed:21568297, PubMed:21950656, RESID:AA0569]
-synonym: "(2S)-5-[(diaminomethylidene)amino]-2-(dimethylamino)pentanoic acid" EXACT RESID-systematic []
-synonym: "(2S)-5-carbamimidamido-2-(dimethylamino)pentanoic acid [tautomer]" EXACT RESID-alternate []
-synonym: "MOD_RES N2,N2-dimethylarginine" EXACT UniProt-feature []
-synonym: "N(alpha),N(alpha)-dimethylarginine" EXACT RESID-alternate []
-synonym: "N2,N2-dimethyl-L-arginine" EXACT RESID-name []
-synonym: "N2,N2-dimethylarginine" EXACT RESID-alternate []
-property_value: DiffAvg "28.05" xsd:float
-property_value: DiffFormula "C 2 H 4 N 0 O 0" xsd:string
-property_value: DiffMono "28.031300" xsd:float
-property_value: Formula "C 8 H 17 N 4 O 1" xsd:string
-property_value: MassAvg "185.25" xsd:float
-property_value: MassMono "185.140236" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0459
-is_a: MOD:00783
-
-[Term]
-id: MOD:01899
-name: L-arginine thiazole-4-carboxylic acid
-def: "A protein modification that effectively crosslinks an L-arginine residue and an L-cysteine residue to form arginine thiazole-4-carboxylic acid." [PubMed:21568297, PubMed:21950656, RESID:AA0570]
-comment: Cross-link 2.
-synonym: "2-[(1S)-1-amino-4-([diaminomethylidene]amino)butyl]-1,3-thiazole-4-carboxylic acid" EXACT RESID-systematic []
-synonym: "CROSSLNK Thiazole-4-carboxylic acid (Arg-Cys)" EXACT UniProt-feature []
-synonym: "L-arginine thiazole-4-carboxylic acid" EXACT RESID-name []
-property_value: DiffAvg "-20.03" xsd:float
-property_value: DiffFormula "C 0 H -4 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-20.026215" xsd:float
-property_value: Formula "C 9 H 13 N 5 O 1 S 1" xsd:string
-property_value: MassAvg "239.30" xsd:float
-property_value: MassMono "239.084081" xsd:float
-property_value: Origin "C, R" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0460
-is_a: MOD:02041
-is_a: MOD:01420
-is_a: MOD:02082
-
-[Term]
-id: MOD:01900
-name: L-cysteine 5-methyloxazole-4-carboxylic acid
-def: "A protein modification that effectively crosslinks an L-cysteine residue and an L-threonine residue to form L-cysteine 5-methyloxazole-4-carboxylic acid." [PubMed:21568297, PubMed:21950656, RESID:AA0571]
-comment: Cross-link 2.
-synonym: "2-[(1R)-1-amino-2-sulfanylethyl]-5-methyl-1,3-oxazole-4-carboxylic acid" EXACT RESID-systematic []
-synonym: "2-[(1R)-1-azanyl-2-sulfanylethyl]-5-methyl-1,3-oxazole-4-carboxylic acid" EXACT RESID-alternate []
-synonym: "CROSSLNK 5-methyloxazole-4-carboxylic acid (Cys-Thr)" EXACT UniProt-feature []
-synonym: "L-cysteine 5-methyloxazole-4-carboxylic acid" EXACT RESID-name []
-property_value: DiffAvg "-20.03" xsd:float
-property_value: DiffFormula "C 0 H -4 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-20.026215" xsd:float
-property_value: Formula "C 7 H 8 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "184.21" xsd:float
-property_value: MassMono "184.030649" xsd:float
-property_value: Origin "C, T" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0461
-is_a: MOD:02044
-is_a: MOD:01422
-is_a: MOD:02082
-
-[Term]
-id: MOD:01901
-name: L-threonine 5-methyloxazole-4-carboxylic acid
-def: "A protein modification that effectively crosslinks two L-threonine residues to form L-threonine 5-methyloxazole-4-carboxylic acid." [PubMed:21568297, PubMed:21950656, RESID:AA0572]
-comment: Cross-link 2.
-synonym: "2-[(1S,2R)-1-amino-2-hydroxypropyl]-5-methyl-1,3-oxazole-4-carboxylic acid" EXACT RESID-systematic []
-synonym: "2-[(1S,2R)-1-azanyl-2-hydroxypropyl]-5-methyl-1,3-oxazole-4-carboxylic acid" EXACT RESID-alternate []
-synonym: "CROSSLNK 5-methyloxazole-4-carboxylic acid (Thr-Thr)" EXACT UniProt-feature []
-synonym: "L-threonine 5-methyloxazole-4-carboxylic acid" EXACT RESID-name []
-property_value: DiffAvg "-20.03" xsd:float
-property_value: DiffFormula "C 0 H -4 N 0 O -1" xsd:string
-property_value: DiffMono "-20.026215" xsd:float
-property_value: Formula "C 8 H 10 N 2 O 3" xsd:string
-property_value: MassAvg "182.18" xsd:float
-property_value: MassMono "182.069142" xsd:float
-property_value: Origin "T, T" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0462
-is_a: MOD:01422
-is_a: MOD:02082
-
-[Term]
-id: MOD:01902
-name: L-isoleucine oxazole-4-carboxylic acid
-def: "A protein modification that effectively crosslinks an L-isoleucine residue and an L-serine residue to form L-cysteine oxazole-4-carboxylic acid." [PubMed:21568297, PubMed:21950656, RESID:AA0573]
-comment: Cross-link 2.
-synonym: "2-[(1S,2S)-1-amino-2-methylbutyl]-1,3-oxazole-4-carboxylic acid" EXACT RESID-systematic []
-synonym: "2-[(1S,2S)-1-azanyl-2-methylbutyl]-1,3-oxazole-4-carboxylic acid" EXACT RESID-alternate []
-synonym: "CROSSLNK Oxazole-4-carboxylic acid (Ile-Ser)" EXACT UniProt-feature []
-synonym: "L-isoleucine oxazole-4-carboxylic acid" EXACT RESID-name []
-property_value: DiffAvg "-20.03" xsd:float
-property_value: DiffFormula "C 0 H -4 N 0 O -1" xsd:string
-property_value: DiffMono "-20.026215" xsd:float
-property_value: Formula "C 9 H 12 N 2 O 2" xsd:string
-property_value: MassAvg "180.21" xsd:float
-property_value: MassMono "180.089878" xsd:float
-property_value: Origin "I, S" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0463
-is_a: MOD:02049
-is_a: MOD:01421
-is_a: MOD:02082
-
-[Term]
-id: MOD:01903
-name: L-serine oxazole-4-carboxylic acid
-def: "A protein modification that effectively crosslinks two L-serine residues to form serine oxazole-4-carboxylic acid." [PubMed:21568297, PubMed:21950656, RESID:AA0574]
-comment: Cross-link 2.
-synonym: "2-[(1S)-1-amino-2-hydroxyethyl]-1,3-oxazole-4-carboxylic acid" EXACT RESID-systematic []
-synonym: "2-[(1S)-1-azanyl-2-hydroxyethyl]-1,3-oxazole-4-carboxylic acid" EXACT RESID-alternate []
-synonym: "CROSSLNK Oxazole-4-carboxylic acid (Ser-Ser)" EXACT UniProt-feature []
-synonym: "L-serine oxazole-4-carboxylic acid" EXACT RESID-name []
-property_value: DiffAvg "-20.03" xsd:float
-property_value: DiffFormula "C 0 H -4 N 0 O -1" xsd:string
-property_value: DiffMono "-20.026215" xsd:float
-property_value: Formula "C 6 H 6 N 2 O 3" xsd:string
-property_value: MassAvg "154.13" xsd:float
-property_value: MassMono "154.037842" xsd:float
-property_value: Origin "S, S" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0464
-is_a: MOD:01421
-is_a: MOD:02082
-
-[Term]
-id: MOD:01904
-name: L-serine 5-methyloxazoline-4-carboxylic acid
-def: "A protein modification that effectively crosslinks an L-serine residue and an L-threonine residue to form L-serine 5-methyloxazoline-4-carboxylic acid." [PubMed:21568297, PubMed:21950656, RESID:AA0575]
-comment: Cross-link 2.
-synonym: "2-[(1S)-1-amino-2-hydroxyethyl]-5-methyl-1,3-oxazoline-4-carboxylic acid" EXACT RESID-alternate []
-synonym: "2-[(1S)-1-amino-2-hydroxyethyl]-5-methyl-4,5-dihydro-1,3-oxazole-4-carboxylic acid" EXACT RESID-systematic []
-synonym: "2-[(1S)-1-azanyl-2-hydroxyethyl]-5-methyl-4,5-dihydro-1,3-oxazole-4-carboxylic acid" EXACT RESID-alternate []
-synonym: "CROSSLNK 5-methyloxazoline-4-carboxylic acid (Ser-Thr)" EXACT UniProt-feature []
-synonym: "L-serine 5-methyloxazoline-4-carboxylic acid" EXACT RESID-name []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 7 H 10 N 2 O 3" xsd:string
-property_value: MassAvg "170.17" xsd:float
-property_value: MassMono "170.069142" xsd:float
-property_value: Origin "S, T" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0465
-is_a: MOD:02055
-is_a: MOD:01422
-is_a: MOD:00954
-
-[Term]
-id: MOD:01905
-name: 5-hydroxy-3-methyl-L-proline
-def: "A protein modification that effectively converts a source amino acid residue to 5-hydroxy-3-methyl-L-proline." [PubMed:7592021, PubMed:8557573, RESID:AA0473]
-synonym: "(2S,3S,5Xi)-5-hydroxy-3-methylpyrrolidine-2-carboxylic acid" EXACT RESID-systematic []
-synonym: "5-hydroxy-3-methyl-L-proline" EXACT RESID-name []
-synonym: "5-hydroxy-3-methylproline" EXACT RESID-alternate []
-synonym: "5Hy3MePro" EXACT PSI-MOD-label []
-synonym: "beta-methyl-delta-hydroxyproline" EXACT RESID-alternate []
-synonym: "MOD_RES 5-hydroxy-3-methylproline (Ile)" EXACT UniProt-feature []
-property_value: Formula "C 6 H 9 N 1 O 2" xsd:string
-property_value: MassAvg "127.14" xsd:float
-property_value: MassMono "127.063329" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00859
-relationship: has_functional_parent MOD:01024
-
-[Term]
-id: MOD:01906
-name: dehydromethionine
-def: "A protein modification that effectively converts an L-methionine residue to dehydromethionine." [PubMed:18688235, PubMed:19775156]
-synonym: "(3S)-3-carboxy-1-methylisothiazolidin-1-ium" EXACT PSI-MOD-alternate []
-synonym: "L-dehydromethionine" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "-1.01" xsd:float
-property_value: DiffFormula "C 0 H -1 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "-1.008374" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 5 H 9 N 1 O 1 S 1" xsd:string
-property_value: MassAvg "131.19" xsd:float
-property_value: MassMono "131.039936" xsd:float
-property_value: Origin "M" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00601
-is_a: MOD:00913
-
-[Term]
-id: MOD:01907
-name: dehydromethionine (from L-methioninium)
-def: "A protein modification that effectively converts an L-methioninium (protonated L-methionine) residue to dehydromethionine." [PubMed:18688235, PubMed:19775156]
-comment: This process accounts only for cyclizaation and not protonation. The alternative process (MOD:01906) accounts for both protonation and cyclization.
-synonym: "(3S)-3-carboxy-1-methylisothiazolidin-1-ium" EXACT PSI-MOD-alternate []
-synonym: "L-dehydromethionine" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "-2.016199" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 5 H 9 N 1 O 1 S 1" xsd:string
-property_value: MassAvg "131.19" xsd:float
-property_value: MassMono "131.039936" xsd:float
-property_value: Origin "MOD:001464" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00601
-is_a: MOD:00913
-relationship: derives_from MOD:01464
-
-[Term]
-id: MOD:01908
-name: 4-sulfophenyl isothiocyanate alpha-amino derivatized residue
-def: "A protein modification that effectively converts a residue to the 4-sulfophenyl isothiocyanate adduct, alpha-amino-[(4-sulfophenyl)carbamothioyl] residue." [PubMed:14689565, PubMed:14745769, PubMed:15549660, PubMed:16526082, Unimod:261#N-term]
-synonym: "4-sulfophenyl isothiocyanate" RELATED Unimod-description []
-synonym: "alpha-amino-[(4-sulfophenyl)carbamothioyl] residue" EXACT PSI-MOD-alternate []
-synonym: "SPITC" RELATED PSI-MS-label []
-property_value: DiffAvg "215.24" xsd:float
-property_value: DiffFormula "C 7 H 5 N 1 O 3 S 2" xsd:string
-property_value: DiffMono "214.971085" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:261
-is_a: MOD:00584
-
-[Term]
-id: MOD:01909
-name: 6x(13)C labeled 4-sulfophenyl isothiocyanate alpha-amino derivatized residue
-def: "A protein modification that effectively converts a residue to the 6x(13)C labeled 4-sulfophenyl isothiocyanate adduct, alpha-amino-[(4-sulfophenyl)carbamothioyl] residue." [PubMed:11467524, PubMed:16526082, Unimod:464#N-term]
-synonym: "4-sulfophenyl isothiocyanate (Heavy C13)" RELATED Unimod-description []
-synonym: "SPITC:13C(6)" RELATED PSI-MS-label []
-property_value: DiffAvg "220.99" xsd:float
-property_value: DiffFormula "(12)C 1 (13)C 6 H 5 N 1 O 3 S 2" xsd:string
-property_value: DiffMono "220.991214" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:464
-is_a: MOD:00880
-
-[Term]
-id: MOD:01910
-name: monofluorinated residue
-def: "A protein modification that effectively substitutes one hydrogen atom of a residue with one fluorine atom." [Unimod:127]
-synonym: "F1Res" EXACT PSI-MOD-label []
-property_value: DiffAvg "17.99" xsd:float
-property_value: DiffFormula "C 0 F 1 H -1 N 0 O 0" xsd:string
-property_value: DiffMono "17.990578" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:127
-is_a: MOD:00498
-
-[Term]
-id: MOD:01911
-name: monochlorinated residue
-def: "A protein modification that effectively substitutes one hydrogen atom of a residue with one chlorine atom." [Unimod:936]
-synonym: "Cl1Res" EXACT PSI-MOD-label []
-property_value: DiffAvg "34.44" xsd:float
-property_value: DiffFormula "C 0 Cl 1 H -1 N 0 O 0" xsd:string
-property_value: DiffMono "33.961028" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:936
-is_a: MOD:00753
-
-[Term]
-id: MOD:01912
-name: monobrominated residue
-def: "A protein modification that effectively substitutes one hydrogen atom of a residue with one bromine atom." [Unimod:340]
-synonym: "Br1Res" EXACT PSI-MOD-label []
-property_value: DiffAvg "78.90" xsd:float
-property_value: DiffFormula "Br 1 C 0 H -1 N 0 O 0" xsd:string
-property_value: DiffMono "77.910512" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-xref: Unimod:340
-is_a: MOD:00754
-
-[Term]
-id: MOD:01913
-name: monochlorinated L-tryptophan
-def: "A protein modification that effectively substitutes one hydrogen atom of an L-tryptophan residue with one chlorine atom." [PubMed:18688235]
-synonym: "Cl1Trp" EXACT PSI-MOD-label []
-property_value: DiffAvg "34.44" xsd:float
-property_value: DiffFormula "C 0 Cl 1 H -1 N 0 O 0" xsd:string
-property_value: DiffMono "33.961028" xsd:float
-property_value: Formula "C 11 Cl 1 H 9 N 2 O 1" xsd:string
-property_value: MassAvg "220.66" xsd:float
-property_value: MassMono "220.040341" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01068
-is_a: MOD:01911
-
-[Term]
-id: MOD:01914
-name: O5-galactosyl-L-hydroxylysine
-def: "A protein modification that effectively converts a 5-hydroxy-L-lysine residue to O5-galactosyl-L-hydroxylysine." [PMID:743239, PubMed:17516569, Unimod:907]
-comment: Secondary to RESID:AA0028. This intermediate is rarely observed [JSG].
-subset: PSI-MOD-slim
-synonym: "Galactosyl hydroxylysine" RELATED Unimod-description []
-synonym: "OGal5HyLys" EXACT PSI-MOD-label []
-synonym: "CARBOHYD O-linked (Gal) hydroxylysine" EXACT UniProt-feature []
-property_value: DiffAvg "162.14" xsd:float
-property_value: DiffFormula "C 6 H 10 O 5" xsd:string
-property_value: DiffMono "162.052823" xsd:float
-property_value: Formula "C 16 H 22 N 2 O 7" xsd:string
-property_value: MassAvg "354.36" xsd:float
-property_value: MassMono "354.142701" xsd:float
-property_value: Origin "MOD:00037" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:907
-xref: uniprot.ptm:PTM-0556
-is_a: MOD:00476
-is_a: MOD:00396
-
-[Term]
-id: MOD:01915
-name: N-formyl-L-alanine
-def: "A protein modification that effectively converts an L-alanine residue to N-formyl-L-alanine." [PubMed:9334739, RESID:AA0576]
-synonym: "(2S)-2-(formylamino)propanoic acid" EXACT RESID-systematic []
-synonym: "2-formamidopropanoic acid" EXACT RESID-alternate []
-synonym: "2-formamidopropionic acid" EXACT RESID-alternate []
-synonym: "N-formyl-L-alanine" EXACT RESID-name []
-property_value: DiffAvg "28.01" xsd:float
-property_value: DiffFormula "C 1 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "27.994915" xsd:float
-property_value: Formula "C 4 H 6 N 1 O 2" xsd:string
-property_value: MassAvg "100.10" xsd:float
-property_value: MassMono "100.039853" xsd:float
-property_value: Origin "A" xsd:string
-property_value: Source "hypothetical" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00409
-is_a: MOD:00901
-
-[Term]
-id: MOD:01916
-name: O4'-(N-acetylamino)galactosyl-L-tyrosine
-def: "A protein modification that effectively converts an L-tyrosine residue to O4'-(N-acetylamino)galactosyl-L-tyrosine." [PubMed:21712440, PubMed:21983924, RESID:AA0577]
-synonym: "(2S)-2-amino-3-(D-2-acetamido-2-deoxygalactopyranosyloxy)phenylpropanoic acid" EXACT RESID-systematic []
-synonym: "CARBOHYD O-linked (GalNAc) tyrosine" EXACT UniProt-feature []
-synonym: "mucin type O-glycosyltyrosine" EXACT RESID-alternate []
-synonym: "O4'-(N-acetylamino)galactosyl-L-tyrosine" EXACT RESID-name []
-synonym: "O4'-(N-acetylgalactosaminyl)tyrosine" EXACT RESID-alternate []
-synonym: "O4'-glycosyl-L-tyrosine" EXACT RESID-alternate []
-property_value: DiffAvg "203.19" xsd:float
-property_value: DiffFormula "C 8 H 13 N 1 O 5" xsd:string
-property_value: DiffMono "203.079373" xsd:float
-property_value: Formula "C 17 H 22 N 2 O 7" xsd:string
-property_value: MassAvg "366.37" xsd:float
-property_value: MassMono "366.142701" xsd:float
-property_value: Origin "Y" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0570
-is_a: MOD:00563
-is_a: MOD:01927
-
-[Term]
-id: MOD:01917
-name: N6-(L-isoaspartyl)-L-lysine (Asp)
-def: "A protein modification that effectively crosslinks an L-aspartic acid residue and an L-lysine residue by an isopeptide bond with the formation of N6-(L-isoaspartyl)-L-lysine and the release of water." [ChEBI:21862, PubMed:11000116, PubMed:15044436, PubMed:18063798, PubMed:6503713, RESID:AA0294#ASP]
-comment: Cross-link 2.
-synonym: "(2S)-2-amino-6-([(3S)-3-amino-3-carboxypropanoyl]amino)hexanoic acid" EXACT RESID-systematic []
-synonym: "beta-(N6-lysyl)aspartyl acid" EXACT RESID-alternate []
-synonym: "CROSSLNK Isoaspartyl lysine isopeptide (Lys-Asn)" EXACT UniProt-feature []
-synonym: "isoaspartyl N6-lysine" EXACT RESID-alternate []
-synonym: "N(epsilon)-(beta-aspartyl)lysine" EXACT RESID-alternate []
-synonym: "N6-(L-isoaspartyl)-L-lysine" EXACT RESID-name []
-synonym: "XLNK-4Asp-N6Lys(Asp)" EXACT PSI-MOD-label []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 10 H 15 N 3 O 3" xsd:string
-property_value: MassAvg "225.25" xsd:float
-property_value: MassMono "225.111341" xsd:float
-property_value: Origin "D, K" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0486
-is_a: MOD:02043
-is_a: MOD:01929
-is_a: MOD:00954
-
-[Term]
-id: MOD:01918
-name: (2S,5S)-5-hydroxylysine
-def: "A protein modification that effectively converts an L-lysine residue to (2S,5S)-5-hydroxylysine." [PubMed:19574390, PubMed:22238144, RESID:AA0578]
-subset: PSI-MOD-slim
-synonym: "(2S,5S)-2,6-diamino-5-hydroxyhexanoic acid" EXACT RESID-systematic []
-synonym: "(2S,5S)-5-hydroxylysine" EXACT RESID-name []
-synonym: "2,6-bisazanyl-5-hydroxyhexanoic acid" EXACT RESID-alternate []
-synonym: "2,6-diamino-2,3,4,6-tetradeoxyhexonic acid" EXACT RESID-alternate []
-synonym: "alpha,epsilon-diamino-delta-hydroxycaproic acid" EXACT RESID-alternate []
-synonym: "L-allo-delta-hydroxylysine" EXACT RESID-alternate []
-synonym: "L-threo-delta-hydroxylysine" EXACT RESID-alternate []
-synonym: "MOD_RES (5S)-5-hydroxylysine" EXACT UniProt-feature []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 6 H 12 N 2 O 2" xsd:string
-property_value: MassAvg "144.17" xsd:float
-property_value: MassMono "144.089878" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0472
-is_a: MOD:00037
-
-[Term]
-id: MOD:01919
-name: (2S,3S)-3-hydroxyaspartic acid
-def: "A protein modification that effectively converts an L-aspartic acid residue to (2S,3S)-3-hydroxyaspartic acid." [ChEBI:10696, PubMed:21177872, RESID:AA0579, ChEBI:138111]
-subset: PSI-MOD-slim
-synonym: "(2S,3S)-2-amino-3-hydroxybutanedioic acid" EXACT RESID-systematic []
-synonym: "(2S,3S)-3-hydroxyaspartic acid" EXACT RESID-name []
-synonym: "(3S)-3-hydroxy-L-aspartic acid" EXACT RESID-alternate []
-synonym: "2-amino-3-hydroxysuccinic acid" EXACT RESID-alternate []
-synonym: "2-azanyl-3-hydroxybutanedioic acid" EXACT RESID-alternate []
-synonym: "3-hydroxyaspartic acid" EXACT RESID-alternate []
-synonym: "L-threo-3-hydroxyaspartic acid" EXACT RESID-alternate []
-synonym: "L-threo-beta-hydroxyaspartic acid" EXACT RESID-alternate []
-synonym: "MOD_RES (3S)-3-hydroxyaspartate" EXACT UniProt-feature []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 4 H 5 N 1 O 4" xsd:string
-property_value: MassAvg "131.09" xsd:float
-property_value: MassMono "131.021858" xsd:float
-property_value: Origin "D" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0473
-is_a: MOD:01926
-
-[Term]
-id: MOD:01920
-name: 3-hydroxy-L-histidine
-def: "A protein modification that effectively converts an L-histidine residue to 3-hydroxy-L-histidine." [PubMed:21251231, RESID:AA0580, ChEBI:138021]
-synonym: "(2S)-2-amino-3-hydroxy-3-(1H-imidazol-4-yl)propanoic acid" EXACT RESID-systematic []
-synonym: "3-hydroxy-L-histidine" EXACT RESID-name []
-synonym: "MOD_RES (3S)-3-hydroxyhistidine" EXACT UniProt-feature []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 6 H 7 N 3 O 2" xsd:string
-property_value: MassAvg "153.14" xsd:float
-property_value: MassMono "153.053826" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0477
-is_a: MOD:00909
-is_a: MOD:00677
-
-[Term]
-id: MOD:01921
-name: D-aspartic acid (Asp)
-def: "A protein modification that effectively converts an L-aspartic acid residue to D-aspartic acid." [ChEBI:48094, PubMed:9384562, RESID:AA0190#ASP]
-synonym: "(2R)-2-aminobutanedioic acid" EXACT RESID-systematic []
-synonym: "2-azanylbutanedioic acid" EXACT RESID-alternate []
-synonym: "aminosuccinic acid" EXACT RESID-alternate []
-synonym: "D-aspartic acid" EXACT RESID-name []
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Formula "C 4 H 5 N 1 O 3" xsd:string
-property_value: MassAvg "115.09" xsd:float
-property_value: MassMono "115.026943" xsd:float
-property_value: Origin "D" xsd:string
-property_value: Source "artifactual" xsd:string
-is_a: MOD:00904
-is_a: MOD:01942
-
-[Term]
-id: MOD:01922
-name: 3-methoxydehydroalanine
-def: "A protein modification that effectively converts an L-serine residue to 3-methoxydehydroalanine." [PubMed:19745839, RESID:AA0582]
-synonym: "2-amino-3-methoxyprop-2-enoic acid" EXACT RESID-systematic []
-synonym: "3-methoxydehydroalanine" EXACT RESID-name []
-synonym: "3-methoxydidehydroalanine" EXACT RESID-alternate []
-property_value: DiffAvg "12.01" xsd:float
-property_value: DiffFormula "C 1 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "12.000000" xsd:float
-property_value: Formula "C 4 H 5 N 1 O 2" xsd:string
-property_value: MassAvg "99.09" xsd:float
-property_value: MassMono "99.032028" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00916
-relationship: has_functional_parent MOD:00189
-
-[Term]
-id: MOD:01923
-name: N6-(L-aspartyl)-L-lysine
-def: "A protein modification that effectively crosslinks an L-aspartic acid residue and an L-lysine residue by an isopeptide bond to form N6-(L-aspartyl)-L-lysine and the release of water." [PubMed:15044436, RESID:AA0583]
-comment: Cross-link 2.
-synonym: "(2S)-2-amino-6-([(2S)-2-amino-3-carboxypropanoyl]amino)hexanoic acid" EXACT RESID-systematic []
-synonym: "alpha-(N6-lysyl)aspartyl acid" EXACT RESID-alternate []
-synonym: "aspartyl N6-lysine" EXACT RESID-alternate []
-synonym: "N(epsilon)-(alpha-aspartyl)lysine" EXACT RESID-alternate []
-synonym: "N6-(L-aspartyl)-L-lysine" EXACT RESID-name []
-synonym: "XLNK-4Asp-N6Lys(Asp)" EXACT PSI-MOD-label []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 10 H 16 N 3 O 4" xsd:string
-property_value: MassAvg "242.26" xsd:float
-property_value: MassMono "242.114081" xsd:float
-property_value: Origin "D, K" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-is_a: MOD:00688
-is_a: MOD:02043
-is_a: MOD:00954
-is_a: MOD:01875
-
-[Term]
-id: MOD:01924
-name: S-octanoyl-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-octanoyl-L-cysteine." [PubMed:12591875, PubMed:16342964, RESID:AA0584]
-synonym: "(2S)-2-amino-3-(octanoylsulfanyl)propanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-3-(octanoylthio)propanoic acid" EXACT RESID-alternate []
-synonym: "ACT_SITE Acyl-thioester intermediate" EXACT UniProt-feature []
-synonym: "cysteine octanoate thioester" EXACT RESID-alternate []
-synonym: "S-octanoyl-L-cysteine" EXACT RESID-name []
-property_value: DiffAvg "126.20" xsd:float
-property_value: DiffFormula "C 8 H 14 N 0 O 1 S 0" xsd:string
-property_value: DiffMono "126.104465" xsd:float
-property_value: Formula "C 11 H 19 N 1 O 2 S 1" xsd:string
-property_value: MassAvg "229.34" xsd:float
-property_value: MassMono "229.113650" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00666
-is_a: MOD:00672
-is_a: MOD:00905
-
-[Term]
-id: MOD:01925
-name: (2S,5R)-5-hydroxylysine
-def: "A protein modification that effectively converts an L-lysine residue to (2S,5R)-5-hydroxylysine." [ChEBI:18040, PubMed:13375629, PubMed:15504407, PubMed:16101297, PubMed:2857489, RESID:AA0028]
-subset: PSI-MOD-slim
-synonym: "(2S,5R)-2,6-diamino-5-hydroxyhexanoic acid" EXACT RESID-systematic []
-synonym: "(2S,5R)-5-hydroxylysine" EXACT RESID-name []
-synonym: "2,6-bisazanyl-5-hydroxyhexanoic acid" EXACT RESID-alternate []
-synonym: "2,6-diamino-2,3,4,6-tetradeoxyhexonic acid" EXACT RESID-alternate []
-synonym: "5-hydroxylated L-lysine" EXACT PSI-MOD-alternate []
-synonym: "5HyLys" EXACT PSI-MOD-label []
-synonym: "alpha,epsilon-diamino-delta-hydroxycaproic acid" EXACT RESID-alternate []
-synonym: "L-erythro-delta-hydroxylysine" EXACT RESID-alternate []
-synonym: "MOD_RES (2S,5R)-5-hydroxylysine" EXACT UniProt-feature []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 6 H 12 N 2 O 2" xsd:string
-property_value: MassAvg "144.17" xsd:float
-property_value: MassMono "144.089878" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0471
-is_a: MOD:00037
-
-[Term]
-id: MOD:01926
-name: 3-hydroxy-L-aspartic acid
-def: "A protein modification that effectively converts an L-aspartic acid residue to one of the diastereomeric 3-hydroxy-L-aspartic acid residues." [OMSSA:59, Unimod:35#D]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-hydroxybutanedioic acid" EXACT PSI-MOD-alternate []
-synonym: "(2S)-3-hydroxyaspartic acid" EXACT PSI-MOD-alternate []
-synonym: "3HyAsp" EXACT PSI-MOD-label []
-synonym: "erythro-beta-hydroxylated L-aspartic acid" EXACT PSI-MOD-alternate []
-synonym: "hydroxylationd" EXACT OMSSA-label []
-synonym: "monohydroxylated aspartic acid" EXACT PSI-MOD-alternate []
-synonym: "Oxidation" RELATED PSI-MS-label []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 4 H 5 N 1 O 4" xsd:string
-property_value: MassAvg "131.09" xsd:float
-property_value: MassMono "131.021858" xsd:float
-property_value: Origin "D" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:35
-is_a: MOD:00425
-is_a: MOD:00904
-
-[Term]
-id: MOD:01927
-name: O-glycosyl-L-tyrosine
-def: "A protein modification that effectively converts an L-tyrosine residue to O4'-glycosyltyrosine." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "OGlycoTyr" EXACT PSI-MOD-label []
-property_value: Origin "Y" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00396
-is_a: MOD:00919
-
-[Term]
-id: MOD:01928
-name: N-(L-isoaspartyl)-glycine
-def: "A protein modification that effectively crosslinks either an L-asparagine residue or an L-aspartic acid residue with a glycine residue by an isopeptide bond with formation of N-(L-isoaspartyl)glycine." [ChEBI:21479, PubMed:1826288, RESID:AA0126]
-comment: Cross-link 2.
-synonym: "(2S)-2-amino-4-(carboxymethyl)amino-4-oxobutanoic acid" EXACT RESID-systematic []
-synonym: "2-amino-N4-(carboxymethyl)-butanediamic acid" EXACT RESID-alternate []
-synonym: "isoaspartyl glycine" EXACT RESID-alternate []
-synonym: "N-(L-isoaspartyl)-glycine" EXACT RESID-name []
-synonym: "N-beta-aspartylglycine" EXACT RESID-alternate []
-synonym: "N4-(carboxymethyl)-asparagine" EXACT RESID-alternate []
-synonym: "XLNK-4Asp-NGly" EXACT PSI-MOD-label []
-property_value: Formula "C 6 H 7 N 2 O 3" xsd:string
-property_value: MassAvg "155.13" xsd:float
-property_value: MassMono "155.045667" xsd:float
-property_value: Origin "G" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00688
-is_a: MOD:02047
-
-[Term]
-id: MOD:01929
-name: N6-(L-isoaspartyl)-L-lysine
-def: "A protein modification that effectively crosslinks an either an L-asparagine residue or an L-aspartic acid residue with an L-lysine residue by an isopeptide bond with the formation of N6-(L-isoaspartyl)-L-lysine." [ChEBI:21862, DeltaMass:0, PubMed:11000116, PubMed:6503713, RESID:AA0294]
-comment: Cross-link 2.
-synonym: "(2S)-2-amino-6-([(3S)-3-amino-3-carboxypropanoyl]amino)hexanoic acid" EXACT RESID-systematic []
-synonym: "beta-(N6-lysyl)aspartyl acid" EXACT RESID-alternate []
-synonym: "CROSSLNK Isoaspartyl lysine isopeptide (Lys-Asn)" EXACT UniProt-feature []
-synonym: "isoaspartyl N6-lysine" EXACT RESID-alternate []
-synonym: "N(epsilon)-(beta-aspartyl)lysine" EXACT RESID-alternate []
-synonym: "N-(beta-Aspartyl)-Lysine (Crosslink)" EXACT DeltaMass-label []
-synonym: "N6-(L-isoaspartyl)-L-lysine" EXACT RESID-name []
-synonym: "XLNK-4Asp-N6Lys" EXACT PSI-MOD-label []
-property_value: Formula "C 10 H 15 N 3 O 3" xsd:string
-property_value: MassAvg "225.25" xsd:float
-property_value: MassMono "225.111341" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00688
-is_a: MOD:01875
-
-[Term]
-id: MOD:01930
-name: D-aspartic acid (Asn)
-def: "A protein modification that effectively converts an L-asparagine residue to D-aspartic acid." [ChEBI:48094, PubMed:9384562, RESID:AA0190#ASN]
-synonym: "(2R)-2-aminobutanedioic acid" EXACT RESID-systematic []
-synonym: "2-azanylbutanedioic acid" EXACT RESID-alternate []
-synonym: "aminosuccinic acid" EXACT RESID-alternate []
-synonym: "D-aspartic acid" EXACT RESID-name []
-property_value: DiffAvg "0.98" xsd:float
-property_value: DiffFormula "C 0 H -1 N -1 O 1" xsd:string
-property_value: DiffMono "0.984016" xsd:float
-property_value: Formula "C 4 H 5 N 1 O 3" xsd:string
-property_value: MassAvg "115.09" xsd:float
-property_value: MassMono "115.026943" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "artifactual" xsd:string
-is_a: MOD:00903
-is_a: MOD:01942
-
-[Term]
-id: MOD:01931
-name: N6-phospho-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-phospho-L-lysine." [PubMed:20144148, RESID:AA0585]
-synonym: "(2S)-2-amino-6-(phosphonoamino)hexanoic acid" EXACT RESID-systematic []
-synonym: "(2S)-2-azanyl-6-(phosphonoamino)hexanoic acid" EXACT RESID-alternate []
-synonym: "6-phospholysine" EXACT RESID-alternate []
-synonym: "N(6)-phosphonolysine" EXACT RESID-alternate []
-synonym: "N(epsilon)-phospholysine" EXACT RESID-alternate []
-synonym: "N(epsilon)-phosphonolysine" EXACT RESID-alternate []
-synonym: "N(epsilon)-phosphonyllysine" EXACT RESID-alternate []
-synonym: "N(epsilon)-phosphoryllysine" EXACT RESID-alternate []
-synonym: "N6-phospho-L-lysine" EXACT RESID-name []
-property_value: DiffAvg "79.98" xsd:float
-property_value: DiffFormula "C 0 H 1 N 0 O 3 P 1" xsd:string
-property_value: DiffMono "79.966331" xsd:float
-property_value: Formula "C 6 H 13 N 2 O 4 P 1" xsd:string
-property_value: MassAvg "208.15" xsd:float
-property_value: MassMono "208.061294" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "hypothetical" xsd:string
-is_a: MOD:00912
-is_a: MOD:01456
-
-[Term]
-id: MOD:01932
-name: L-lysinonorleucine
-def: "A protein modification that effectively cross-links two lysine residues with a carbon-nitrogen bond to form L-lysinonorleucine.." [PubMed:5117030, PubMed:5817620, PubMed:5879466, PubMed:6030254, RESID:AA0586]
-comment: Cross-link 2.
-synonym: "(2S)-2-amino-6-([(5S)-5-amino-5-carboxypentyl]amino)hexanoic acid" EXACT RESID-systematic []
-synonym: "(2S,2'S)-6,6'-iminobis(2-aminohexanoic acid)" EXACT RESID-alternate []
-synonym: "6-(N6-L-lysino)-L-norleucine" EXACT RESID-alternate []
-synonym: "L-lysinonorleucine" EXACT RESID-name []
-synonym: "lysinonorleucine" EXACT RESID-alternate []
-synonym: "lysinorleucine [misspelling]" EXACT RESID-alternate []
-synonym: "lysylnorleucine" EXACT RESID-alternate []
-synonym: "N6-[(5S)-5-amino-5-carboxypentyl]-L-lysine" EXACT RESID-alternate []
-property_value: DiffAvg "-17.03" xsd:float
-property_value: DiffFormula "C 0 H -3 N -1 O 0" xsd:string
-property_value: DiffMono "-17.026549" xsd:float
-property_value: Formula "C 12 H 21 N 3 O 2" xsd:string
-property_value: MassAvg "239.32" xsd:float
-property_value: MassMono "239.163377" xsd:float
-property_value: Origin "K, K" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:02051
-is_a: MOD:00946
-
-[Term]
-id: MOD:01933
-name: desmosine
-def: "A protein modification that effectively cross-links four L-lysine residues to form desmosine." [ChEBI:37629, PubMed:13941623, PubMed:14109938, PubMed:14109939, PubMed:5839176, RESID:AA0587]
-comment: Cross-link 4.
-synonym: "4-[(4S)-4-amino-4-carboxybutyl]-1-[(5S)-5-amino-5-carboxypentyl]-3,5-bis[(3S)-3-amino-3-carboxypropyl]pyridinium" EXACT RESID-systematic []
-synonym: "6-[4-(4-amino-4-carboxybutyl)-3,5-bis(3-amino-3-carboxypropyl)pyridinio]norleucine" EXACT RESID-alternate []
-synonym: "desmosine" EXACT RESID-name []
-property_value: DiffAvg "-58.15" xsd:float
-property_value: DiffFormula "C 0 H -16 N -3 O 0" xsd:string
-property_value: DiffMono "-58.134971" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 24 H 32 N 5 O 4" xsd:string
-property_value: MassAvg "454.55" xsd:float
-property_value: MassMono "454.244881" xsd:float
-property_value: Origin "K, K, K, K" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:02051
-is_a: MOD:01425
-
-[Term]
-id: MOD:01934
-name: isodesmosine
-def: "A protein modification that effectively cross-links four L-lysine residues to form isodesmosine." [ChEBI:37629, PubMed:13941623, PubMed:14109938, PubMed:14109939, PubMed:5839176, RESID:AA0588]
-comment: Cross-link 4.
-synonym: "2-[(4S)-4-amino-4-carboxybutyl]-1-[(5S)-5-amino-5-carboxypentyl]-3,5-bis[(3S)-3-amino-3-carboxypropyl]pyridinium" EXACT RESID-systematic []
-synonym: "6-[2-(4-amino-4-carboxybutyl)-3,5-bis(3-amino-3-carboxypropyl)pyridinio]norleucine" EXACT RESID-alternate []
-synonym: "isodesmosine" EXACT RESID-name []
-property_value: DiffAvg "-58.15" xsd:float
-property_value: DiffFormula "C 0 H -16 N -3 O 0" xsd:string
-property_value: DiffMono "-58.134971" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 24 H 32 N 5 O 4" xsd:string
-property_value: MassAvg "454.55" xsd:float
-property_value: MassMono "454.244881" xsd:float
-property_value: Origin "K, K, K, K" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:02051
-is_a: MOD:01425
-
-[Term]
-id: MOD:01935
-name: O-glucosyl-L-hydroxylysine
-def: "modification from RESID" [PubMed:22045808, RESID:AA0589]
-synonym: "(D-glucopyranosyl)oxy-L-lysine" EXACT RESID-systematic []
-synonym: "O-glucosyl-L-hydroxylysine" EXACT RESID-name []
-synonym: "CARBOHYD O-linked (Glc) hydroxylysine" EXACT UniProt-feature []
-property_value: DiffAvg "178.14" xsd:float
-property_value: DiffFormula "C 6 H 10 N 0 O 6" xsd:string
-property_value: DiffMono "178.047738" xsd:float
-property_value: Formula "C 12 H 22 N 2 O 7" xsd:string
-property_value: MassAvg "306.32" xsd:float
-property_value: MassMono "306.142701" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0572
-relationship: derives_from MOD:01047
-is_a: MOD:00396
-is_a: MOD:00912
-
-[Term]
-id: MOD:01936
-name: N6-oleoyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-oleoyl-L-lysine." [PubMed:20942504, RESID:AA0590]
-synonym: "(2S)-2-amino-6-([(9Z)-octadec-9-enoyl]amino)hexanoic acid" EXACT RESID-systematic []
-synonym: "N6-[(9Z)-1-oxo-9-octadecenyl]lysine" EXACT RESID-alternate []
-synonym: "N6-oleoyl-L-lysine" EXACT RESID-name []
-property_value: DiffAvg "264.45" xsd:float
-property_value: DiffFormula "C 18 H 32 N 0 O 1" xsd:string
-property_value: DiffMono "264.245316" xsd:float
-property_value: Formula "C 24 H 44 N 2 O 2" xsd:string
-property_value: MassAvg "392.63" xsd:float
-property_value: MassMono "392.340279" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:01875
-is_a: MOD:02011
-
-[Term]
-id: MOD:01937
-name: N-palmitoyl-L-methionine
-def: "A protein modification that effectively converts an L-methionine residue to N-palmitoyl-L-methionine." [PubMed:20942504, RESID:AA0591]
-synonym: "(2S)-2-(hexadecanoylamino)-4-(methylsulfanyl)butanoic acid" EXACT RESID-systematic []
-synonym: "2-(hexadecanamido)-4-(methylsulfanyl)butanoic acid" EXACT RESID-alternate []
-synonym: "LIPID N-palmitoyl methionine" EXACT UniProt-feature []
-synonym: "N-(1-oxohexadecyl)methionine" EXACT RESID-alternate []
-synonym: "N-palmitoyl-L-methionine" EXACT RESID-name []
-property_value: DiffAvg "238.41" xsd:float
-property_value: DiffFormula "C 16 H 30 N 0 O 1 S 0" xsd:string
-property_value: DiffMono "238.229666" xsd:float
-property_value: Formula "C 21 H 40 N 1 O 2 S 1" xsd:string
-property_value: MassAvg "370.62" xsd:float
-property_value: MassMono "370.277976" xsd:float
-property_value: Origin "M" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00913
-is_a: MOD:01685
-
-[Term]
-id: MOD:01938
-name: 2-(2-aminosuccinimidyl)-3-sulfanylpropanoic acid (Asn)
-def: "A protein modification that crosslinks an asparagine and the following cysteine residue with the formation of (2-aminosuccinimidyl)-3-sulfanylpropanoic acid and the release of ammonia." [RESID:AA0592#ASN]
-comment: Cross-link 2.
-synonym: "(2R)-2-[(3S)-3-amino-2,5-dioxopyrrolidin-1-yl]-3-sulfanylpropanoic acid" EXACT RESID-systematic []
-synonym: "2-(2-aminosuccinimidyl)-3-sulfanylpropanoic acid" EXACT RESID-name []
-synonym: "aspartimide cysteine" EXACT RESID-alternate []
-property_value: DiffAvg "-17.03" xsd:float
-property_value: DiffFormula "C 0 H -3 N -1 O 0 S 0" xsd:string
-property_value: DiffMono "-17.026549" xsd:float
-property_value: Formula "C 7 H 8 N 2 O 3 S 1" xsd:string
-property_value: MassAvg "200.21" xsd:float
-property_value: MassMono "200.025563" xsd:float
-property_value: Origin "C, N" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:02042
-is_a: MOD:01945
-is_a: MOD:00946
-
-[Term]
-id: MOD:01939
-name: 2-(2-aminosuccinimidyl)-3-sulfanylpropanoic acid (Asp)
-def: "A protein modification that crosslinks an aspartic acid and the following cysteine residue with the formation of (2-aminosuccinimidyl)-3-sulfanylpropanoic acid and the loss of a water molecule." [RESID:AA0592#ASP]
-comment: Cross-link 2.
-synonym: "(2R)-2-[(3S)-3-amino-2,5-dioxopyrrolidin-1-yl]-3-sulfanylpropanoic acid" EXACT RESID-systematic []
-synonym: "2-(2-aminosuccinimidyl)-3-sulfanylpropanoic acid" EXACT RESID-name []
-synonym: "aspartimide cysteine" EXACT RESID-alternate []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 7 H 8 N 2 O 3 S 1" xsd:string
-property_value: MassAvg "200.21" xsd:float
-property_value: MassMono "200.025563" xsd:float
-property_value: Origin "C, D" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:02043
-is_a: MOD:01945
-is_a: MOD:00954
-
-[Term]
-id: MOD:01940
-name: 2-(2-aminosuccinimidyl)pentanedioic acid (Asn)
-def: "A protein modification that crosslinks an asparagine and the following glutamic acid residue with the formation of (2-aminosuccinimidyl)pentanedioic acid and the release of ammonia." [RESID:AA0593#ASN]
-comment: Cross-link 2.
-synonym: "(4S)-4-[(3S)-3-amino-2,5-dioxopyrrolidin-1-yl]-5-oxopentanoic acid" EXACT RESID-systematic []
-synonym: "2-(2-aminosuccinimidyl)pentanedioic acid" EXACT RESID-name []
-synonym: "aspartimide glutamic acid" EXACT RESID-alternate []
-property_value: DiffAvg "-17.03" xsd:float
-property_value: DiffFormula "C 0 H -3 N -1 O 0" xsd:string
-property_value: DiffMono "-17.026549" xsd:float
-property_value: Formula "C 9 H 10 N 2 O 5" xsd:string
-property_value: MassAvg "226.19" xsd:float
-property_value: MassMono "226.058971" xsd:float
-property_value: Origin "E, N" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:02042
-is_a: MOD:01946
-is_a: MOD:00946
-
-[Term]
-id: MOD:01941
-name: 2-(2-aminosuccinimidyl)pentanedioic acid (Asp)
-def: "A protein modification that crosslinks an aspartic acid and the following glycine residue with the formation of (2-aminosuccinimidyl)pentanedioic acid and the loss of a water molecule." [RESID:AA0593#ASP]
-comment: Cross-link 2.
-synonym: "(4S)-4-[(3S)-3-amino-2,5-dioxopyrrolidin-1-yl]-5-oxopentanoic acid" EXACT RESID-systematic []
-synonym: "2-(2-aminosuccinimidyl)pentanedioic acid" EXACT RESID-name []
-synonym: "aspartimide glutamic acid" EXACT RESID-alternate []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 9 H 10 N 2 O 5" xsd:string
-property_value: MassAvg "226.19" xsd:float
-property_value: MassMono "226.058971" xsd:float
-property_value: Origin "D, E" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:02043
-is_a: MOD:01946
-is_a: MOD:00954
-
-[Term]
-id: MOD:01942
-name: D-aspartic acid
-def: "A protein modification that effectively converts a source amino acid residue to D-aspartic acid." [ChEBI:48094, PubMed:9384562, RESID:AA0190]
-synonym: "(2R)-2-aminobutanedioic acid" EXACT RESID-systematic []
-synonym: "2-azanylbutanedioic acid" EXACT RESID-alternate []
-synonym: "aminosuccinic acid" EXACT RESID-alternate []
-synonym: "D-aspartic acid" EXACT RESID-name []
-property_value: Formula "C 4 H 5 N 1 O 3" xsd:string
-property_value: MassAvg "115.09" xsd:float
-property_value: MassMono "115.026943" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifactual" xsd:string
-is_a: MOD:00664
-is_a: MOD:00859
-
-[Term]
-id: MOD:01943
-name: pyrrolidione ring crosslinked residues
-def: "A protein modification that crosslinks two adjacent residues by formation of a pyrrolidione ring." [PubMed:18688235]
-is_a: MOD:00033
-
-[Term]
-id: MOD:01944
-name: 2-aminosuccinimide ring crosslinked residues
-def: "A protein modification that forms (2-aminosuccinimidyl)acetic acid by crosslinking either an aspartic acid residue or an asparagine residue with the following residue." [PubMed:18688235]
-comment: Cross-link 2; this cross-link is formed by the condensation of an aspartic acid residue or an asparagine residue with the alpha-amido of the following residue.
-subset: PSI-MOD-slim
-property_value: Origin "X" xsd:string
-property_value: Source "hypothetical" xsd:string
-is_a: MOD:00033
-is_a: MOD:00859
-
-[Term]
-id: MOD:01945
-name: 2-(2-aminosuccinimidyl)-3-sulfanylpropanoic acid
-def: "A protein modification that forms (2-aminosuccinimidyl)-3-sulfanylpropanoic acid by crosslinking either an aspartic acid residue or an asparagine residue with the following cysteine residue." [PubMed:18688235]
-comment: Cross-link 2; this cross-link is formed by the condensation of an aspartic acid residue or an asparagine residue with the alpha-amido of the following residue.
-property_value: Formula "C 6 H 6 N 2 O 3" xsd:string
-property_value: MassAvg "154.13" xsd:float
-property_value: MassMono "154.037842" xsd:float
-property_value: Origin "C, X" xsd:string
-property_value: Source "hypothetical" xsd:string
-is_a: MOD:02044
-is_a: MOD:01944
-
-[Term]
-id: MOD:01946
-name: 2-(2-aminosuccinimidyl)pentanedioic acid
-def: "A protein modification that forms (2-aminosuccinimidyl)pentanedioicacid by crosslinking either an aspartic acid residue or an asparagine residue with the following glutamic acid\n residue." [PubMed:18688235]
-comment: Cross-link 2; this cross-link is formed by the condensation of an aspartic acid residue or an asparagine residue with the alpha-amido of the following residue.
-property_value: Formula "C 6 H 6 N 2 O 3" xsd:string
-property_value: MassAvg "154.13" xsd:float
-property_value: MassMono "154.037842" xsd:float
-property_value: Origin "E, X" xsd:string
-property_value: Source "hypothetical" xsd:string
-is_a: MOD:02045
-is_a: MOD:01944
-
-[Term]
-id: MOD:01947
-name: O-(L-isoaspartyl)-L-threonine (cross-link)
-def: "A protein modification that effectively cross-links an L-threonine residue and an L-aspartic acid residue with an ester bond to form  O-(L-isoaspartyl)-L-threonine." [PubMed:17157318, PubMed:8706862, RESID:AA0525#TDX]
-comment: Cross-link 2.
-synonym: "(2S)-2-amino-4-([(1S,2R)-1-amino-1-carboxypropan-2-yl]oxy)-4-oxobutanoic acid" EXACT RESID-systematic []
-synonym: "(2S,3R)-2-amino-3-([(4S)-3-amino-3-carboxypropanoyl]oxy)propanoic acid" EXACT RESID-alternate []
-synonym: "CROSSLNK isoaspartyl threonine ester (Thr-Asp)" EXACT UniProt-feature []
-synonym: "O(beta)-(beta-aspartyl)threonine" EXACT RESID-alternate []
-synonym: "O-(L-isoaspartyl)-L-threonine" EXACT RESID-name []
-synonym: "O3-(isoaspartyl)-threonine" EXACT RESID-alternate []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 8 H 10 N 2 O 4" xsd:string
-property_value: MassAvg "198.18" xsd:float
-property_value: MassMono "198.064057" xsd:float
-property_value: Origin "D, T" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00885
-is_a: MOD:02043
-is_a: MOD:00954
-is_a: MOD:01978
-
-[Term]
-id: MOD:01948
-name: labionin
-def: "A protein modification that effectively cross-links an L-cysteine residue and two L-serine residues by a thioether bond and a carbon-carbon bond to form labionin." [PubMed:20082397, RESID:AA0594]
-comment: Cross-link 3.
-synonym: "(2S,4S)-2,4-diamino-2-[([(2R)-2-amino-2-carboxyethyl]sulfanyl)methyl]pentanedioic acid" EXACT RESID-systematic []
-synonym: "(2S,4S,8R)-2,4,8-triamino-4-carboxy-6-thianonanedioic acid" EXACT RESID-alternate []
-synonym: "(2S,4S,8R)-labionin" EXACT RESID-alternate []
-synonym: "labionin" EXACT RESID-name []
-property_value: DiffAvg "-36.03" xsd:float
-property_value: DiffFormula "C 0 H -4 N 0 O -2 S 0" xsd:string
-property_value: DiffMono "-36.021129" xsd:float
-property_value: Formula "C 9 H 11 N 3 O 3 S 1" xsd:string
-property_value: MassAvg "241.26" xsd:float
-property_value: MassMono "241.052112" xsd:float
-property_value: Origin "C, S, S" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:02055
-is_a: MOD:01993
-
-[Term]
-id: MOD:01949
-name: coelenterazine
-def: "A protein modification that effectively cross-links a phenylalanine and two tyrosine residues to form coelenterazine." [ChEBI:2311, PubMed:10830969, PubMed:11572972, PubMed:19833098, RESID:AA0595]
-comment: Cross-link 3.
-synonym: "8-benzyl-2-(4-hydroxybenzyl)-6-(4-hydroxyphenyl)imidazo[1,2-a]pyrazin-3(7H)-one" EXACT RESID-systematic []
-synonym: "coelenterazine" EXACT RESID-name []
-synonym: "Oplophorus luciferin" EXACT RESID-alternate []
-property_value: DiffAvg "-50.06" xsd:float
-property_value: DiffFormula "C -1 H -6 N 0 O -2" xsd:string
-property_value: DiffMono "-50.036779" xsd:float
-property_value: Formula "C 26 H 21 N 3 O 3" xsd:string
-property_value: MassAvg "423.47" xsd:float
-property_value: MassMono "423.158292" xsd:float
-property_value: Origin "F, Y, Y" xsd:string
-property_value: Source "hypothetical" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00033
-is_a: MOD:02053
-is_a: MOD:02058
-
-[Term]
-id: MOD:01950
-name: L-isoglutamyl histamine
-def: "A protein modification that effectively converts an L-glutamine residue to L-isoglutamyl histamine." [PubMed:23022564, RESID:AA0596]
-synonym: "(2S)-2-amino-5-([2-(1H-imidazol-5-yl)ethyl]amino)-5-oxopentanoic acid" EXACT RESID-systematic []
-synonym: "(gamma-glutamyl)histamine" EXACT RESID-alternate []
-synonym: "L-isoglutamyl histamine" EXACT RESID-name []
-property_value: DiffAvg "94.12" xsd:float
-property_value: DiffFormula "C 5 H 6 N 2 O 0" xsd:string
-property_value: DiffMono "94.053098" xsd:float
-property_value: Formula "C 10 H 14 N 4 O 2" xsd:string
-property_value: MassAvg "222.25" xsd:float
-property_value: MassMono "222.111676" xsd:float
-property_value: Origin "Q" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0488
-is_a: MOD:00907
-
-[Term]
-id: MOD:01951
-name: O-(L-isoglutamyl)-L-serine (Gln-Ser)
-def: "A protein modification that effectively crosslinks an L-glutamine residue and an L-serine residue by an ester bond and releasing ammonia to form O-(L-isoglutamyl)-L-serine." [PubMed:17051152, RESID:AA0597#QSX]
-comment: Cross-link 2.
-synonym: "(2S)-2-amino-5-[(2S)-2-amino-2-carboxyethoxy]-5-oxopentanoic acid" EXACT RESID-systematic []
-synonym: "O(beta)-(gamma-glutamyl)serine" EXACT RESID-alternate []
-synonym: "O-(L-isoglutamyl)-L-serine" EXACT RESID-name []
-synonym: "O3-(isoglutamyl)-serine" EXACT RESID-alternate []
-property_value: DiffAvg "-17.03" xsd:float
-property_value: DiffFormula "C 0 H -3 N -1 O 0" xsd:string
-property_value: DiffMono "-17.026549" xsd:float
-property_value: Formula "C 8 H 10 N 2 O 4" xsd:string
-property_value: MassAvg "198.18" xsd:float
-property_value: MassMono "198.064057" xsd:float
-property_value: Origin "Q, S" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:02046
-is_a: MOD:00946
-is_a: MOD:01977
-
-[Term]
-id: MOD:01952
-name: O-(L-isoglutamyl)-L-threonine (Gln-Thr)
-def: "A protein modification that effectively cross-links an L-threonine residue and an L-glutamine residue with an ester bond releasing ammonia to form O-(L-isoglutamyl)-L-threonine." [PubMed:17051152, RESID:AA0536#TQX]
-comment: Cross-link 2.
-synonym: "(2S)-2-amino-5-([(1S,2R)-1-amino-1-carboxypropan-2-yl]oxy)-5-oxopentanoic acid" EXACT RESID-systematic []
-synonym: "(2S,3R)-2-amino-3-([(4S)-4-amino-4-carboxybutanoyl]oxy)-propanoic acid" EXACT RESID-alternate []
-synonym: "5-(threon-O3-yl)glutamate" EXACT RESID-alternate []
-synonym: "O(beta)-(gamma-glutamyl)threonine" EXACT RESID-alternate []
-synonym: "O-(L-isoglutamyl)-L-threonine" EXACT RESID-name []
-synonym: "O3-(isoglutamyl)threonine" EXACT RESID-alternate []
-property_value: DiffAvg "-17.03" xsd:float
-property_value: DiffFormula "C 0 H -3 N -1 O 0" xsd:string
-property_value: DiffMono "-17.026549" xsd:float
-property_value: Formula "C 9 H 12 N 2 O 4" xsd:string
-property_value: MassAvg "212.20" xsd:float
-property_value: MassMono "212.079707" xsd:float
-property_value: Origin "Q, T" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:02046
-is_a: MOD:02056
-is_a: MOD:01979
-is_a: MOD:00885
-is_a: MOD:00946
-
-[Term]
-id: MOD:01953
-name: tetrakis-L-cysteinyl tetrairon octanitrosyl
-def: "A protein modification that effectively converts four L-cysteine residues and a four-iron cluster to tetrakis-L-cysteinyl tetrairon octanitrosyl." [PubMed:21182249, RESID:AA0599]
-comment: Cross-link 4.
-property_value: DiffAvg "459.40" xsd:float
-property_value: DiffFormula "C 0 Fe 4 H -4 N 8 O 8 S 0" xsd:string
-property_value: DiffMono "459.692359" xsd:float
-property_value: Formula "C 12 Fe 4 H 16 N 12 O 12 S 4" xsd:string
-property_value: MassAvg "871.95" xsd:float
-property_value: MassMono "871.729098" xsd:float
-property_value: Origin "C, C, C, C" xsd:string
-property_value: Source "hypothetical" xsd:string
-is_a: MOD:00738
-is_a: MOD:02067
-
-[Term]
-id: MOD:01954
-name: dehydroalanine (Sec)
-def: "A protein modification that effectively converts an L-selenocysteine residue to dehydroalanine." [ChEBI:17123, PubMed:10220322, PubMed:12781460, PubMed:1547888, PubMed:1815586, PubMed:20805503, PubMed:21420488, PubMed:22031445, PubMed:2914619, PubMed:7947813, PubMed:8239649, RESID:AA0181]
-synonym: "2,3-didehydroalanine" EXACT RESID-alternate []
-synonym: "2-aminoacrylic acid" EXACT RESID-alternate []
-synonym: "2-aminopropenoic acid" EXACT RESID-systematic []
-synonym: "4-methylidene-imidazole-5-one (MIO) active site" EXACT RESID-alternate []
-synonym: "anhydroserine" EXACT RESID-alternate []
-synonym: "dehydroalanine" EXACT RESID-name []
-synonym: "Dha" EXACT RESID-alternate []
-property_value: DiffAvg "-80.99" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0 Se -1" xsd:string
-property_value: DiffMono "-81.932171" xsd:float
-property_value: Formula "C 3 H 3 N 1 O 1" xsd:string
-property_value: MassAvg "69.06" xsd:float
-property_value: MassMono "69.021464" xsd:float
-property_value: Origin "U" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:01158
-is_a: MOD:01168
-
-[Term]
-id: MOD:01955
-name: L-alaninato bis-L-aspartato tris-L-glutamato L-histidino calcium tetramanganese pentoxide
-def: "modification from RESID" [PubMed:21499260, RESID:AA0600]
-comment: Cross-link 7.
-synonym: "4Mn-Ca-5O cluster" EXACT RESID-alternate []
-synonym: "L-alaninato bis-L-aspartato tris-L-glutamato L-histidino calcium tetramanganese pentoxide" EXACT RESID-name []
-synonym: "mu2-alaninato-1kappaO(1),3kappaO(1')-mu2-aspartato-1kappaO(4),5kappaO(4')-mu2-aspartato-2kappaO(4),3kappaO(4')-mu2-glutamato-3kappaO(5),4kappaO(5')-mu2-glutamato-4kappaO(5),5kappaO(5')-mu-glutamato-2kappaO(5)-mu-histidino-2kappaN(tau)-mu4-oxido-1:2:4:5kappa(4)O-tri-mu3-oxido-1:2:3kappa(3)O;1:3:4kappa(3)O;2:3:4kappa(3)O;mu-oxido-4:5kappa(2)O-calciumtetramanganese" EXACT RESID-systematic []
-synonym: "photosystem II catalytic cluster" EXACT RESID-alternate []
-property_value: DiffAvg "333.78" xsd:float
-property_value: DiffFormula "C 0 Ca 1 H -6 Mn 4 N 0 O 5" xsd:string
-property_value: DiffMono "333.642394" xsd:float
-property_value: Formula "C 32 Ca 1 H 38 Mn 4 N 9 O 23" xsd:string
-property_value: MassAvg "1176.53" xsd:float
-property_value: MassMono "1175.922825" xsd:float
-property_value: Origin "A, D, D, E, E, E, H" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "C-term" xsd:string
-is_a: MOD:00740
-is_a: MOD:01482
-is_a: MOD:02065
-is_a: MOD:02066
-is_a: MOD:02068
-is_a: MOD:02070
-
-[Term]
-id: MOD:01956
-name: (3R)-3-hydroxy-L-arginine
-def: "A protein modification that effectively converts an L-arginine residue to (3R)-3-hydroxy-L-arginine." [PubMed:10094780, PubMed:23103944, PubMed:786730, RESID:AA0601]
-synonym: "(2S,3R)-2-amino-5-[(diaminomethylidene)amino]-3-hydroxypentanoic acid" EXACT RESID-systematic []
-synonym: "(3R)-3-hydroxy-L-arginine" EXACT RESID-name []
-synonym: "2-amino-5-(carbamimidamido)-3-hydroxypentanoic acid [tautomer]" EXACT RESID-alternate []
-synonym: "2-amino-5-[(aminoiminomethyl)amino]-3-hydroxypentanoic acid [tautomer]" EXACT RESID-alternate []
-synonym: "2-amino-5-guanidino-3-hydroxypentanoic acid" EXACT RESID-alternate []
-synonym: "beta-hydroxyarginine" EXACT RESID-alternate []
-synonym: "C(beta)-hydroxyarginine" EXACT RESID-alternate []
-synonym: "MOD_RES (3R)-3-hydroxyarginine" EXACT UniProt-feature []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 6 H 12 N 4 O 2" xsd:string
-property_value: MassAvg "172.19" xsd:float
-property_value: MassMono "172.096026" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0476
-is_a: MOD:00682
-
-[Term]
-id: MOD:01957
-name: 2-hydroxyproline
-def: "A protein modification that effectively converts an L-proline residue to 2-hydroxyproline." [PubMed:23385463, RESID:AA0602, ChEBI:141809]
-synonym: "(2R)-2-hydroxypyrrolidine-2-carboxylic acid" EXACT RESID-systematic []
-synonym: "2-hydroxyproline" EXACT RESID-name []
-synonym: "2-oxidanylpyrrolidine-2-carboxylic acid" EXACT RESID-alternate []
-synonym: "alpha-hydroxyproline" EXACT RESID-alternate []
-synonym: "MOD_RES 2-hydroxyproline" EXACT UniProt-feature []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 5 H 7 N 1 O 2" xsd:string
-property_value: MassAvg "113.12" xsd:float
-property_value: MassMono "113.047678" xsd:float
-property_value: Origin "P" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: uniprot.ptm:PTM-0668
-is_a: MOD:01024
-
-[Term]
-id: MOD:01958
-name: bis-L-cysteinyl bisglutathion-S-yl diiron disulfide
-def: "A protein modification that effectively converts four L-cysteine residues and a two-iron two-sulfur cluster to bis-L-cysteinyl bisglutathion-S-yl diiron disulfide." [PubMed:17121859, RESID:AA0603]
-comment: Cross-link 2.
-synonym: "bis-L-cysteinyl bisglutathion-S-yl diiron disulfide" EXACT RESID-name []
-synonym: "di-mu-sulfido-bis(cysteinato)-1kappaS,2kappaS-bis(glutathionato)-1kappaS,2kappaS-diiron" EXACT RESID-systematic []
-synonym: "mitochondrial glutaredoxin 2 dimer iron-sulfur cluster" EXACT RESID-alternate []
-synonym: "plant glutaredoxin C1 dimer iron-sulfur cluster" EXACT RESID-alternate []
-property_value: DiffAvg "786.42" xsd:float
-property_value: DiffFormula "C 20 Fe 2 H 30 N 6 O 12 S 4" xsd:string
-property_value: DiffMono "785.950329" xsd:float
-property_value: Formula "C 26 Fe 2 H 40 N 8 O 14 S 6" xsd:string
-property_value: MassAvg "992.70" xsd:float
-property_value: MassMono "991.968699" xsd:float
-property_value: Origin "C, C" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00739
-is_a: MOD:02067
-
-[Term]
-id: MOD:01959
-name: tris-L-cysteinyl L-glutamato tetrairon tetrasulfide
-def: "A protein modification that effectively converts three L-cysteine residues, an L-glutamic acid and a four-iron four-sulfur cluster to tris-L-cysteinyl L-glutamato tetrairon tetrasulfide." [PubMed:21167158, RESID:AA0604]
-comment: Cross-link 4.
-synonym: "tris-L-cysteinyl L-glutamato tetrairon tetrasulfide" EXACT RESID-name []
-synonym: "tris-mu3-sulfido-tris(cysteinato)-1kappaS,2kappaS,3kappaS-glutamato-4kappaO(5),4kappaO(5')-tetrairon" EXACT RESID-systematic []
-property_value: DiffAvg "347.59" xsd:float
-property_value: DiffFormula "C 0 Fe 4 H -4 N 0 O 0 S 4" xsd:string
-property_value: DiffMono "347.596734" xsd:float
-property_value: Formula "C 14 Fe 4 H 18 N 4 O 6 S 7" xsd:string
-property_value: MassAvg "786.12" xsd:float
-property_value: MassMono "785.666881" xsd:float
-property_value: Origin "C, C, C, E" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00739
-is_a: MOD:02067
-is_a: MOD:02068
-
-[Term]
-id: MOD:01960
-name: tris-L-cysteinyl L-glutamin-O6-yl tetrairon tetrasulfide
-def: "A protein modification that effectively converts three L-cysteine residues, an L-glutamine residue and a four-iron four-sulfur cluster to tris-L-cysteinyl L-glutamin-O6-yl tetrairon tetrasulfide." [PubMed:11796730, RESID:AA0605]
-comment: Cross-link 4.
-synonym: "METAL Iron-sulfur (4Fe-4S)" EXACT UniProt-feature []
-synonym: "tris-L-cysteinyl L-glutamin-O6-yl tetrairon tetrasulfide" EXACT RESID-name []
-synonym: "tris-mu3-sulfido-tris(cysteinato)-1kappaS,2kappaS,3kappaS-glutaminato-4kappaN(5)-tetrairon" EXACT RESID-systematic []
-property_value: DiffAvg "347.59" xsd:float
-property_value: DiffFormula "C 0 Fe 4 H -4 N 0 O 0 S 4" xsd:string
-property_value: DiffMono "347.596734" xsd:float
-property_value: Formula "C 14 Fe 4 H 19 N 5 O 5 S 7" xsd:string
-property_value: MassAvg "785.14" xsd:float
-property_value: MassMono "784.682866" xsd:float
-property_value: Origin "C, C, C, Q" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00739
-is_a: MOD:02067
-is_a: MOD:02069
-
-[Term]
-id: MOD:01961
-name: O-(L-isoglutamyl)-L-threonine (THR)
-def: "OBSOLETE because redundant and identical to MOD:01785. Remap to MOD:01785." [PubMed:16618936, PubMed:17051152, PubMed:17687277, PubMed:18555071, RESID:AA0536#THR]
-synonym: "(2S)-2-amino-5-([(1S,2R)-1-amino-1-carboxypropan-2-yl]oxy)-5-oxopentanoic acid" EXACT RESID-systematic []
-synonym: "(2S,3R)-2-amino-3-([(4S)-4-amino-4-carboxybutanoyl]oxy)-propanoic acid" EXACT RESID-alternate []
-synonym: "5-(threon-O3-yl)glutamate" EXACT RESID-alternate []
-synonym: "O(beta)-(gamma-glutamyl)threonine" EXACT RESID-alternate []
-synonym: "O-(L-isoglutamyl)-L-threonine" EXACT RESID-name []
-synonym: "O3-(isoglutamyl)threonine" EXACT RESID-alternate []
-property_value: DiffAvg "129.12" xsd:float
-property_value: DiffFormula "C 5 H 7 N 1 O 3" xsd:string
-property_value: DiffMono "129.042593" xsd:float
-property_value: Formula "C 9 H 14 N 2 O 5" xsd:string
-property_value: MassAvg "230.22" xsd:float
-property_value: MassMono "230.090272" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-replaced_by: MOD:01785
-is_obsolete: true
-
-[Term]
-id: MOD:01962
-name: N4-(2,4-diacetamido-2,4,6-trideoxy-D-glucosyl)-L-asparagine
-def: "A protein modification that effectively converts an L-asparagine residue to N4-(2,4-diacetamido-2,4,6-trideoxy-D-glucosyl)-L-asparagine." [PubMed:12186869, PubMed:19236052, RESID:AA0606]
-synonym: "(2S)-2-amino-4-[(2,4-diacetylamino-2,4,6-trideoxy-beta-D-glucopyranosyl)amino]-4-oxobutanoic acid" EXACT RESID-systematic []
-synonym: "DABA" EXACT RESID-alternate []
-synonym: "DATDH" EXACT RESID-alternate []
-synonym: "DiNAcBac" EXACT RESID-alternate []
-synonym: "N4-(2,4-diacetamido-2,4,6-trideoxy-D-glucosyl)-L-asparagine" EXACT RESID-name []
-synonym: "N4-[2,4-bis(acetylamino)-2,4,6-trideoxy-beta-D-glucopyranosyl]-L-asparagine" EXACT RESID-alternate []
-synonym: "N4-[N,N-diacetylbacillosaminyl]asparagine" EXACT RESID-alternate []
-synonym: "N4-[N2,N4-diacetylbacillosaminyl]asparagine" EXACT RESID-alternate []
-synonym: "CARBOHYD N-linked (DATDGlc) asparagine" EXACT UniProt-feature []
-property_value: DiffAvg "228.25" xsd:float
-property_value: DiffFormula "C 10 H 16 N 2 O 4" xsd:string
-property_value: DiffMono "228.111007" xsd:float
-property_value: Formula "C 14 H 22 N 4 O 6" xsd:string
-property_value: MassAvg "342.35" xsd:float
-property_value: MassMono "342.153934" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0506
-is_a: MOD:00160
-
-[Term]
-id: MOD:01963
-name: O-(2,4-diacetamido-2,4,6-trideoxy-D-glucosyl)-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O-(2,4-diacetamido-2,4,6-trideoxy-D-glucosyl)-L-serine." [PubMed:23030644, RESID:AA0607]
-synonym: "(2S)-2-amino-4-[(2,4-diacetamido-2,4,6-trideoxy-beta-D-glucopyranosyl)oxy]propanoic acid" EXACT RESID-systematic []
-synonym: "DABA" EXACT RESID-alternate []
-synonym: "DATDH" EXACT RESID-alternate []
-synonym: "DiNAcBac" EXACT RESID-alternate []
-synonym: "O-(2,4-diacetamido-2,4,6-trideoxy-D-glucosyl)-L-serine" EXACT RESID-name []
-synonym: "O-[2,4-bis(acetylamino)-2,4,6-trideoxy-beta-D-glucopyranosyl]-L-serine" EXACT RESID-alternate []
-synonym: "O-[N,N-diacetylbacillosaminyl]serine" EXACT RESID-alternate []
-synonym: "O-[N2,N4-diacetylbacillosaminyl]serine" EXACT RESID-alternate []
-synonym: "CARBOHYD O-linked (DATDGlc) serine" EXACT UniProt-feature []
-property_value: DiffAvg "228.25" xsd:float
-property_value: DiffFormula "C 10 H 16 N 2 O 4" xsd:string
-property_value: DiffMono "228.111007" xsd:float
-property_value: Formula "C 13 H 21 N 3 O 6" xsd:string
-property_value: MassAvg "315.33" xsd:float
-property_value: MassMono "315.143035" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0548
-is_a: MOD:00002
-
-[Term]
-id: MOD:01964
-name: O-(2-acetamido-4-glyceramido-2,4,6-trideoxy-D-glucosyl)-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O-(2-acetamido-4-glyceramido-2,4,6-trideoxy-D-glucosyl)-L-serine." [PubMed:17804791, RESID:AA0608]
-synonym: "(2S)-2-amino-3-[(2-acetamido-4-glycerylamino-2,4,6-trideoxy-D-glucopyranosyl)oxy]propanoic acid" EXACT RESID-systematic []
-synonym: "GATDH" EXACT RESID-alternate []
-synonym: "O-(2-acetamido-4-glyceramido-2,4,6-trideoxy-D-glucopyranosyl)-L-serine" EXACT RESID-alternate []
-synonym: "O-(2-acetamido-4-glyceramido-2,4,6-trideoxy-D-glucosyl)-L-serine" EXACT RESID-name []
-synonym: "O-(N2-acetyl-N4-glycerylbacillosaminyl)-L-serine" EXACT RESID-alternate []
-synonym: "CARBOHYD O-linked (GATDGlc) serine" EXACT UniProt-feature []
-property_value: DiffAvg "274.27" xsd:float
-property_value: DiffFormula "C 11 H 18 N 2 O 6" xsd:string
-property_value: DiffMono "274.116486" xsd:float
-property_value: Formula "C 14 H 23 N 3 O 8" xsd:string
-property_value: MassAvg "361.35" xsd:float
-property_value: MassMono "361.148515" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0549
-is_a: MOD:00002
-
-[Term]
-id: MOD:01965
-name: 2xC(13),3x(2)H labeled N6-acetyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to 2xC(13),3x(2)H labeled N6-acetyl-L-lysine." [PubMed:18688235]
-synonym: "Acetate labeling reagent (K) (heavy form, +5amu)" EXACT PSI-MOD-alternate []
-synonym: "COFRADIC heavy acetyl 13C2 2H3" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "47.04" xsd:float
-property_value: DiffFormula "(13)C 2 (1)H -1 (2)H 3 O 1" xsd:string
-property_value: DiffMono "47.036105" xsd:float
-property_value: Formula "(12)C 6 (13)C 2 (1)H 11 (2)H 3 N 2 O 2" xsd:string
-property_value: MassAvg "175.13" xsd:float
-property_value: MassMono "175.131068" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "artifact" xsd:string
-relationship: derives_from MOD:00064
-is_a: MOD:01428
-is_a: MOD:01431
-
-[Term]
-id: MOD:01966
-name: L-methionine (R)-sulfoxide
-def: "OBSOLETE because redundant and identical to MOD:00720. Remap to MOD:00720." [ChEBI:45764, PubMed:21406390, PubMed:22116028, PubMed:23911929, RESID:AA0581]
-synonym: "(2S)-2-amino-4-[(R)-methylsulfinyl]butanoic acid" EXACT RESID-systematic []
-synonym: "L-methionine (R)-S-oxide" EXACT RESID-alternate []
-synonym: "L-methionine (R)-sulfoxide" EXACT RESID-name []
-synonym: "MOD_RES Methionine (R)-sulfoxide" EXACT UniProt-feature []
-property_value: DiffAvg "16.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 1 S 0" xsd:string
-property_value: DiffMono "15.994915" xsd:float
-property_value: Formula "C 5 H 9 N 1 O 2 S 1" xsd:string
-property_value: MassAvg "147.19" xsd:float
-property_value: MassMono "147.035400" xsd:float
-property_value: Origin "M" xsd:string
-property_value: Source "natural" xsd:string
-replaced_by: MOD:00720
-is_obsolete: true
-
-[Term]
-id: MOD:01967
-name: omega-N-(N-acetylamino)glucosyl-L-arginine
-def: "A protein modification that effectively converts an L-arginine residue to  omega-N-(N-acetylamino)glucosyl-L-arginine." [PubMed:23955153, RESID:AA0609]
-synonym: "(2S)-2-amino-5-[(amino[(2-N-acetylamino-2-deoxy-D-glucopyranosyl)amino]methylidene)amino]pentanoic acid" EXACT RESID-systematic []
-synonym: "N(omega)-(2-acetamido-2-deoxy-D-glucopyranosyl)-L-arginine" EXACT RESID-alternate []
-synonym: "N(omega)-(2-acetylamino-2-deoxy-D-glucopyranosyl)-L-arginine" EXACT RESID-alternate []
-synonym: "N(omega)-(2-N-acetylaminoglucosyl)arginine" EXACT RESID-alternate []
-synonym: "NG-(2-acetamido-2-deoxy-D-glucopyranosyl)-L-arginine" EXACT RESID-alternate []
-synonym: "NG-(2-acetylamino-2-deoxy-D-glucopyranosyl)-L-arginine" EXACT RESID-alternate []
-synonym: "NG-(2-N-acetylaminoglucosyl)arginine" EXACT RESID-alternate []
-synonym: "omega-N-(2-acetamido-2-deoxy-D-glucopyranosyl)-L-arginine" EXACT RESID-alternate []
-synonym: "omega-N-(2-acetylamino-2-deoxy-D-glucopyranosyl)-L-arginine" EXACT RESID-alternate []
-synonym: "omega-N-(2-N-acetylaminoglucosyl)arginine" EXACT RESID-alternate []
-synonym: "omega-N-(N-acetylamino)glucosyl-L-arginine" EXACT RESID-name []
-synonym: "CARBOHYD N-linked (GlcNAc) arginine" EXACT UniProt-feature []
-property_value: DiffAvg "203.19" xsd:float
-property_value: DiffFormula "C 8 H 13 N 1 O 5" xsd:string
-property_value: DiffMono "203.079373" xsd:float
-property_value: Formula "C 14 H 25 N 5 O 6" xsd:string
-property_value: MassAvg "359.38" xsd:float
-property_value: MassMono "359.180484" xsd:float
-property_value: Origin "R" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0518
-is_a: MOD:00448
-is_a: MOD:01980
-
-[Term]
-id: MOD:01968
-name: (2R,3R,2'R)-3-methyllanthionine
-def: "A protein modification that effectively cross-links an L-cysteine residue and an L-threonine residue by a thioether bond to form (2R,3R,2'R)-3-methyllanthionine." [PubMed:23314913, RESID:AA0610]
-comment: Cross-link 2.
-synonym: "(2R,3R)-2-amino-3-([(2R)-2-amino-2-carboxyethyl]sulfanyl)butanoic acid" EXACT RESID-systematic []
-synonym: "(2R,3R,2'R)-2-amino-3-[(2-amino-2-carboxyethyl)thio]butanoic acid" EXACT RESID-alternate []
-synonym: "(2R,3R,2'R)-3-methyllanthionine" EXACT RESID-name []
-synonym: "(2R,3R,6R)-2,6-diamino-3-methyl-4-thiaheptanedioic acid" EXACT RESID-alternate []
-synonym: "(2R,3R,6R)-3-methyllanthionine" EXACT RESID-alternate []
-synonym: "2-azanyl-3-[(2-azanyl-2-carboxyethyl)sulfanyl]butanoic acid" EXACT RESID-alternate []
-synonym: "3-methyl-L,L-lanthionine" EXACT RESID-alternate []
-synonym: "cysteine-3-L-butyrine thioether" EXACT RESID-alternate []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 7 H 10 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "186.23" xsd:float
-property_value: MassMono "186.046299" xsd:float
-property_value: Origin "C, T" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:01981
-
-[Term]
-id: MOD:01969
-name: S-(gamma-glutamyl-cysteinyl-glycyl)-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-(gamma-glutamyl-cysteinyl-glycyl)-cysteine." [PubMed:9398217, RESID:AA0611]
-synonym: "(2S)-2-amino-5-([(2R)-1-([2-([(2R)-2-amino-2-carboxyethyl]sulfanyl)-2-oxoethyl]amino)-1-oxo-3-sulfanylpropan-2-yl]amino)-5-oxopentanoic acid" EXACT RESID-systematic []
-synonym: "ACT_SITE S-(gamma-glutamyl-cysteinyl-glycyl)-cysteine intermediate" EXACT UniProt-feature []
-synonym: "S-(gamma-glutamyl-cysteinyl-glycyl)-cysteine" EXACT RESID-name []
-synonym: "S-(glutathion-1-yl)-L-cysteine" EXACT RESID-alternate []
-property_value: DiffAvg "289.31" xsd:float
-property_value: DiffFormula "C 10 H 15 N 3 O 5 S 1" xsd:string
-property_value: DiffMono "289.073242" xsd:float
-property_value: Formula "C 13 H 20 N 4 O 6 S 2" xsd:string
-property_value: MassAvg "392.44" xsd:float
-property_value: MassMono "392.082426" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00860
-is_a: MOD:00905
-
-[Term]
-id: MOD:01970
-name: 5-glutamyl glutamic acid
-def: "A protein modification that effectively converts an L-glutamic acid residue to 5-glutamyl glutamic acid, forming an isopeptide bond with a free glutamic acid." [PubMed:10747868, PubMed:15525938, PubMed:1680872, PubMed:23434852, RESID:AA0612, Unimod:450]
-synonym: "(2S)-2-([(4S)-4-amino-4-carboxybutanoyl]amino)pentanedioic acid" EXACT RESID-systematic []
-synonym: "(2S)-2-[(4S)-4-amino-4-carboxybutanamido]pentanedioic acid" EXACT RESID-alternate []
-synonym: "2-([4-azanyl-4-carboxybutanoyl]azanyl)pentanedioic acid" EXACT RESID-alternate []
-synonym: "5-glutamyl glutamic acid" EXACT RESID-name []
-synonym: "gamma-glutamylglutamate" EXACT RESID-alternate []
-synonym: "Glu" RELATED Unimod-interim []
-synonym: "isoglutamyl glutamic acid" EXACT RESID-alternate []
-synonym: "isoglutamyl monoglutamic acid" EXACT RESID-alternate []
-synonym: "MOD_RES 5-glutamyl glutamate" EXACT UniProt-feature []
-synonym: "monoglutamyl" RELATED Unimod-description []
-synonym: "N alpha -(gamma-Glutamyl)-Glu" EXACT DeltaMass-label []
-synonym: "N-(gamma-L-glutamyl)-L-glutamic acid" EXACT RESID-alternate []
-property_value: DiffAvg "129.12" xsd:float
-property_value: DiffFormula "C 5 H 7 N 1 O 3" xsd:string
-property_value: DiffMono "129.042593" xsd:float
-property_value: Formula "C 10 H 14 N 2 O 6" xsd:string
-property_value: MassAvg "258.23" xsd:float
-property_value: MassMono "258.085186" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:450
-xref: uniprot.ptm:PTM-0479
-is_a: MOD:00207
-
-[Term]
-id: MOD:01971
-name: 5-glutamyl N2-ornithine
-def: "A protein modification that effectively converts an L-glutamic acid residue to N2-ornithine." [PubMed:23434852, RESID:AA0613, ChEBI:136763]
-synonym: "(2S)-5-amino-2-([(4S)-4-amino-4-carboxybutanoyl]amino)pentanoic acid" EXACT RESID-alternate []
-synonym: "(2S)-5-amino-2-[(4S)-4-amino-4-carboxybutanamido]pentanoic acid" EXACT RESID-systematic []
-synonym: "4-amino-5-[(4-amino-1-carboxy-butyl)amino]-5-ketovaleric acid" EXACT RESID-alternate []
-synonym: "4-amino-5-[(4-amino-1-carboxy-butyl)amino]-5-oxopentanoic acid" EXACT RESID-alternate []
-synonym: "5-glutamyl N2-ornithine" EXACT RESID-name []
-synonym: "gamma-glutamylornithine" EXACT RESID-alternate []
-synonym: "MOD_RES 5-glutamyl N2-ornithine" EXACT UniProt-feature []
-synonym: "N2-(gamma-glutamyl)ornithine" EXACT RESID-alternate []
-synonym: "N2-(L-isoglutamyl)-L-ornithine" EXACT RESID-alternate []
-property_value: DiffAvg "114.15" xsd:float
-property_value: DiffFormula "C 5 H 10 N 2 O 1" xsd:string
-property_value: DiffMono "114.079313" xsd:float
-property_value: Formula "C 10 H 17 N 3 O 4" xsd:string
-property_value: MassAvg "243.26" xsd:float
-property_value: MassMono "243.121906" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "hypothetical" xsd:string
-xref: uniprot.ptm:PTM-0478
-is_a: MOD:00906
-
-[Term]
-id: MOD:01972
-name: 5-glutamyl coenzyme A thioester
-def: "A protein modification that effectively converts an L-glutamic acid residue to 5-glutamyl coenzyme A thioester." [PubMed:16253988, PubMed:20977214, PubMed:7915164, RESID:AA0614]
-synonym: "(2S)-2-amino-5-(2-[([3-([(2R)-2-hydroxy-3,3-dimethyl-4-([3'-phospho-adenosyl-5'-diphosphoryl]-oxy)-butanoyl]-amino)-propanoyl]-amino)-ethyl]-sulfanyl)-5-oxopentanoic acid" EXACT RESID-alternate []
-synonym: "(2S)-2-amino-5-([2-(3-[(2R)-2-hydroxy-3,3-dimethyl-4-([3'-phospho-adenosyl-5'-diphosphoryl]-oxy)-butanamido]-propanamido)-ethyl]-sulfanyl)-5-oxopentanoic acid" EXACT RESID-systematic []
-synonym: "5-glutamyl 4-[(3'-phospho-adenosyl-5'-diphosphoryl)oxy]pantetheine thioester" EXACT RESID-alternate []
-synonym: "5-glutamyl coenzyme A thioester" EXACT RESID-name []
-synonym: "5-glutamyl coenzyme A thioester intermediate" EXACT UniProt-feature []
-property_value: DiffAvg "749.52" xsd:float
-property_value: DiffFormula "C 21 H 34 N 7 O 15 P 3 S 1" xsd:string
-property_value: DiffMono "749.104644" xsd:float
-property_value: Formula "C 26 H 41 N 8 O 18 P 3 S 1" xsd:string
-property_value: MassAvg "878.63" xsd:float
-property_value: MassMono "878.147237" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00860
-is_a: MOD:00861
-is_a: MOD:00906
-
-[Term]
-id: MOD:01973
-name: N6-(3-phosphoglyceryl)-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-(3-phosphoglyceryl)-L-lysine." [PubMed:23908237, RESID:AA0615]
-synonym: "(2S)-2-amino-6-([(2R)-2-hydroxy-3-(phosphonooxy)propanoyl]amino)hexanoic acid" EXACT RESID-alternate []
-synonym: "(2S)-2-amino-6-[(2R)-2-hydroxy-3-(phosphonooxy)propanamido]hexanoic acid" EXACT RESID-systematic []
-synonym: "3-phosphoglyceryl-lysine" EXACT RESID-alternate []
-synonym: "N6-(3-phosphoglyceryl)-L-lysine" EXACT RESID-name []
-property_value: DiffAvg "168.04" xsd:float
-property_value: DiffFormula "C 3 H 5 N 0 O 6 P 1" xsd:string
-property_value: DiffMono "167.982375" xsd:float
-property_value: Formula "C 9 H 17 N 2 O 7 P 1" xsd:string
-property_value: MassAvg "296.22" xsd:float
-property_value: MassMono "296.077338" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00861
-is_a: MOD:01875
-
-[Term]
-id: MOD:01974
-name: S-methyl-L-methionine
-def: "A protein modification that effectively converts an L-methionine residue to S-methyl-L-methionine." [ChEBI:17728, PubMed:23532849, RESID:AA0616]
-synonym: "(2S)-2-amino-4-(dimethylsulfonio)butanoate" EXACT RESID-alternate []
-synonym: "(3S)-(3-amino-3-carboxypropyl)dimethylsulfanium" EXACT RESID-systematic []
-synonym: "[(3S)-3-amino-3-carboxypropyl](dimethyl)sulfonium" EXACT RESID-alternate []
-synonym: "S-methyl-L-methionine" EXACT RESID-name []
-synonym: "S-methylmethionine" EXACT RESID-alternate []
-synonym: "S-methylmethioninium" EXACT RESID-alternate []
-synonym: "vitamin U" EXACT RESID-alternate []
-property_value: DiffAvg "15.03" xsd:float
-property_value: DiffFormula "C 1 H 3 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "15.022927" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 6 H 12 N 1 O 1 S 1" xsd:string
-property_value: MassAvg "146.23" xsd:float
-property_value: MassMono "146.063411" xsd:float
-property_value: Origin "M" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0636
-is_a: MOD:00716
-
-[Term]
-id: MOD:01975
-name: S-poly(3-hydroxybutyrate)-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to S-(poly-3-hydroxybutyrate)-L-cysteine." [PubMed:19711985, PubMed:9888824, RESID:AA0617]
-synonym: "(alpha)-([(2R)-2-amino-2-carboxyethyl]sulfanyl)-(omega)-[(3R)-3-hydroxybutanoyl]-poly([(3R)-3-methyl-1-oxopropane-1,3-diyl]oxy)" EXACT RESID-systematic []
-synonym: "S-poly(3-hydroxybutanoate)cysteine" EXACT RESID-alternate []
-synonym: "S-poly(3-hydroxybutanoic acid)cysteine" EXACT RESID-alternate []
-synonym: "S-poly(3-hydroxybutyrate)-L-cysteine" EXACT RESID-name []
-synonym: "S-poly(3-hydroxybutyrate)cysteine" EXACT RESID-alternate []
-synonym: "S-poly(3-hydroxybutyric acid)cysteine" EXACT RESID-alternate []
-synonym: "S-poly(beta-hydroxybutyrate)cysteine" EXACT RESID-alternate []
-synonym: "S-poly[(R)-3-hydroxybutyrate]cysteine" EXACT RESID-alternate []
-synonym: "MOD_RES S-poly(beta-hydroxybutyryl)lysine" EXACT UniProt-feature []
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0641
-is_a: MOD:00672
-is_a: MOD:00905
-
-[Term]
-id: MOD:01976
-name: O3-(poly-3-hydroxybutyrate)-L-serine
-def: "A protein modification that effectively converts an L-serine residue to O3-(poly-3-hydroxybutyrate)-L-serine." [PubMed:17659252, PubMed:20004640, RESID:AA0618]
-subset: PSI-MOD-slim
-synonym: "(2S)-2-amino-3-[([(3R)-3-hydroxybutanoyl]oxy)-poly([(3R)-3-methyl-1-oxopropane-1,3-diyl]oxy)]propanoic acid" EXACT RESID-systematic []
-synonym: "O3-(poly-3-hydroxybutyrate)-L-serine" EXACT RESID-name []
-synonym: "O3-poly(3-hydroxybutanoate)serine" EXACT RESID-alternate []
-synonym: "O3-poly(3-hydroxybutanoic acid)serine" EXACT RESID-alternate []
-synonym: "O3-poly(3-hydroxybutyrate)serine" EXACT RESID-alternate []
-synonym: "O3-poly(3-hydroxybutyric acid)serine" EXACT RESID-alternate []
-synonym: "O3-poly(beta-hydroxybutyrate)serine" EXACT RESID-alternate []
-synonym: "O3-poly[(R)-3-hydroxybutyrate]serine" EXACT RESID-alternate []
-synonym: "MOD_RES O3-poly(beta-hydroxybutyryl)lysine" EXACT UniProt-feature []
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0640
-is_a: MOD:00671
-is_a: MOD:00916
-
-[Term]
-id: MOD:01977
-name: O-(L-isoglutamyl)-L-serine
-def: "A protein modification that effectively crosslinks either an L-glutamine residue or an L-glutamic acid residue with an L-serine residue by an ester bond  to form O-(L-isoglutamyl)-L-serine." [PubMed:17051152, RESID:AA0597]
-comment: Cross-link 2.
-synonym: "(2S)-2-amino-5-[(2S)-2-amino-2-carboxyethoxy]-5-oxopentanoic acid" EXACT RESID-systematic []
-synonym: "O(beta)-(gamma-glutamyl)serine" EXACT RESID-alternate []
-synonym: "O-(L-isoglutamyl)-L-serine" EXACT RESID-name []
-synonym: "O3-(isoglutamyl)-serine" EXACT RESID-alternate []
-property_value: Formula "C 8 H 10 N 2 O 4" xsd:string
-property_value: MassAvg "198.18" xsd:float
-property_value: MassMono "198.064057" xsd:float
-property_value: Origin "S, X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00859
-is_a: MOD:00885
-is_a: MOD:02055
-
-[Term]
-id: MOD:01978
-name: O-(L-isoaspartyl)-L-threonine
-def: "A protein modification that effectively converts an L-threonine residue to O-(L-isoaspartyl)-L-threonine, using either free L-asparagine and releasing ammonia or using a peptidyl L-aspartic acid residue and releasing water." [PubMed:8706862, RESID:AA0525]
-comment: This is a threonine active intermediate and not an ester cross-link of peptides [JSG].
-synonym: "(2S)-2-amino-4-([(1S,2R)-1-amino-1-carboxypropan-2-yl]oxy)-4-oxobutanoic acid" EXACT RESID-systematic []
-synonym: "(2S,3R)-2-amino-3-([(4S)-3-amino-3-carboxypropanoyl]oxy)propanoic acid" EXACT RESID-alternate []
-synonym: "O(beta)-(beta-aspartyl)threonine" EXACT RESID-alternate []
-synonym: "O-(L-isoaspartyl)-L-threonine" EXACT RESID-name []
-synonym: "O3-(isoaspartyl)-threonine" EXACT RESID-alternate []
-property_value: Formula "C 8 H 12 N 2 O 5" xsd:string
-property_value: MassAvg "216.19" xsd:float
-property_value: MassMono "216.074621" xsd:float
-property_value: Origin "T, X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00859
-is_a: MOD:02056
-
-[Term]
-id: MOD:01979
-name: O-(L-isoglutamyl)-L-threonine
-def: "A protein modification that effectively converts an L-threonine residue to O-(L-isoglutamyl)-L-threonine, using free L-glutamine and releasing ammonia, or using a peptidyl L-glutamine and releasing ammonia." [PubMed:8706862, RESID:AA0536]
-comment: This is not an ester cross-link of peptides [JSG].
-synonym: "(2S)-2-amino-5-([(1S,2R)-1-amino-1-carboxypropan-2-yl]oxy)-5-oxopentanoic acid" EXACT RESID-systematic []
-synonym: "(2S,3R)-2-amino-3-([(4S)-4-amino-4-carboxybutanoyl]oxy)-propanoic acid" EXACT RESID-alternate []
-synonym: "5-(threon-O3-yl)glutamate" EXACT RESID-alternate []
-synonym: "O(beta)-(gamma-glutamyl)threonine" EXACT RESID-alternate []
-synonym: "O-(L-isoglutamyl)-L-threonine" EXACT RESID-name []
-synonym: "O3-(isoglutamyl)threonine" EXACT RESID-alternate []
-property_value: Formula "C 9 H 14 N 2 O 5" xsd:string
-property_value: MassAvg "230.22" xsd:float
-property_value: MassMono "230.090272" xsd:float
-property_value: Origin "T, X" xsd:string
-property_value: Source "hypothetical" xsd:string
-is_a: MOD:00859
-is_a: MOD:02056
-
-[Term]
-id: MOD:01980
-name: omega-N-glycosyl-L-arginine
-def: "A protein modification that effectively converts an L-arginine residue to N4-glycosyl-arginine." [PubMed:15279557, PubMed:8521968, PubMed:9536051, RESID:AA0327, Unimod:41#R]
-synonym: "(2S)-2-amino-5-(beta-D-glucopyranosyl[imino(methylamino)methyl]amino)pentanoic acid" EXACT RESID-systematic []
-synonym: "Hex" RELATED PSI-MS-label []
-synonym: "Hexose" RELATED Unimod-description []
-synonym: "NG-beta-D-glucosylarginine" EXACT RESID-alternate []
-synonym: "omega-N-(beta-D-glucosyl)-L-arginine" EXACT RESID-alternate []
-synonym: "omega-N-glucosyl-L-arginine" EXACT RESID-name []
-synonym: "omega-N-glycosyl-L-arginine" EXACT RESID-alternate []
-property_value: Origin "R" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:41
-is_a: MOD:00006
-is_a: MOD:00902
-
-[Term]
-id: MOD:01981
-name: 3-methyllanthionine
-def: "A protein modification that effectively cross-links an L-cysteine residue and an L-threonine residue by a thioether bond to form 3-methyllanthionine with unresolved stereospecificity." [PubMed:18688235]
-comment: Cross-link 2.
-synonym: "2,6-diamino-3-methyl-4-thiaheptanedioic acid" EXACT PSI-MOD-alternate []
-synonym: "2-amino-3-([2-amino-2-carboxyethyl]sulfanyl)butanoic acid" EXACT PSI-MOD-alternate []
-synonym: "2-amino-3-[(2-amino-2-carboxyethyl)thio]butanoic acid" EXACT PSI-MOD-alternate []
-synonym: "2-azanyl-3-[(2-azanyl-2-carboxyethyl)sulfanyl]butanoic acid" EXACT PSI-MOD-alternate []
-synonym: "3-methyllanthionine" EXACT PSI-MOD-alternate []
-synonym: "cysteine-3-L-butyrine thioether" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "-18.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O -1 S 0" xsd:string
-property_value: DiffMono "-18.010565" xsd:float
-property_value: Formula "C 7 H 10 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "186.23" xsd:float
-property_value: MassMono "186.046299" xsd:float
-property_value: Origin "C, T" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:02056
-is_a: MOD:00954
-is_a: MOD:01993
-
-[Term]
-id: MOD:01982
-name: N,N,N-trimethylglycine
-def: "modification from RESID" [ChEBI:17750, PubMed:23818633, PubMed:23978223, RESID:AA0619]
-subset: PSI-MOD-slim
-synonym: "(trimethylammonio)ethanoic acid" EXACT RESID-alternate []
-synonym: "1-carboxy-N,N,N-trimethylmethanazanium" EXACT RESID-alternate []
-synonym: "2-trimethylammonioacetate" EXACT RESID-alternate []
-synonym: "betaine" EXACT RESID-alternate []
-synonym: "carboxy-N,N,N-trimethylmethanaminium" EXACT RESID-systematic []
-synonym: "carboxymethyl-trimethylazanium" EXACT RESID-alternate []
-synonym: "glycine betaine" EXACT RESID-alternate []
-synonym: "MOD_RES N,N,N-trimethylglycine" EXACT UniProt-feature []
-synonym: "N,N,N-trimethylglycine cation" EXACT RESID-alternate []
-synonym: "N,N,N-trimethylglycinium" EXACT RESID-alternate []
-synonym: "N2Me3+Gly" EXACT PSI-MOD-label []
-property_value: DiffAvg "43.09" xsd:float
-property_value: DiffFormula "C 3 H 7 N 0 O 0" xsd:string
-property_value: DiffMono "43.054775" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 5 H 11 N 1 O 1" xsd:string
-property_value: MassAvg "101.15" xsd:float
-property_value: MassMono "101.084064" xsd:float
-property_value: Origin "G" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0485
-is_a: MOD:00714
-is_a: MOD:01698
-
-[Term]
-id: MOD:01983
-name: N,N-dimethylglycine
-def: "A protein modification that effectively converts a glycine residue to N,N-dimethyllglycine." [ChEBI:17724, PubMed:23818633, PubMed:23978223, RESID:AA0620]
-synonym: "(dimethylamino)ethanoic acid" EXACT RESID-systematic []
-synonym: "1-carboxy-N,N-dimethylaminomethane" EXACT RESID-alternate []
-synonym: "2-(dimethylamino)acetic acid" EXACT RESID-alternate []
-synonym: "MOD_RES N,N-dimethylglycine" EXACT UniProt-feature []
-synonym: "vitamin B16" EXACT RESID-alternate []
-property_value: DiffAvg "28.05" xsd:float
-property_value: DiffFormula "C 2 H 4 N 0 O 0" xsd:string
-property_value: DiffMono "28.031300" xsd:float
-property_value: Formula "C 4 H 8 N 1 O 1" xsd:string
-property_value: MassAvg "86.11" xsd:float
-property_value: MassMono "86.060589" xsd:float
-property_value: Origin "G" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: uniprot.ptm:PTM-0484
-is_a: MOD:00714
-is_a: MOD:01686
-
-[Term]
-id: MOD:01984
-name: 2-(L-cystein-S-yl)-L-alanine
-def: "A protein modification that effectively cross-links an L-cysteine residue and an L-alanine residue by a thioether bond to form 2-(S-L-cysteinyl)-L-alanine." [PubMed:21526839, RESID:AA0621]
-comment: Cross-link 2.
-synonym: "(2R)-2-amino-2-[(2R)-2-amino-2-carboxyethyl]sulfanyl-3-hydroxybutanoic acid" EXACT RESID-systematic []
-synonym: "(2R,5R)-2,5-diamino-5-methyl-4-thiahexanedioic acid" EXACT RESID-alternate []
-synonym: "alpha-(L-cystein-S-yl)-L-alanine" EXACT RESID-alternate []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 6 H 8 N 2 O 2 S 1" xsd:string
-property_value: MassAvg "172.20" xsd:float
-property_value: MassMono "172.030649" xsd:float
-property_value: Origin "A, C" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:02040
-is_a: MOD:01992
-
-[Term]
-id: MOD:01985
-name: 2-(L-cystein-S-yl)-D-asparagine
-def: "A protein modification that effectively cross-links an L-cysteine residue and an L-asparagine residue by a thioether bond to form 2-(S-L-cysteinyl)-D-asparagine." [PubMed:21786372, RESID:AA0622]
-comment: Cross-link 2.
-synonym: "(2S)-2,4-diamino-2-([(2R)-2-amino-2-carboxyethyl]sulfanyl)-4-oxobutanoic acid" EXACT RESID-systematic []
-synonym: "alpha-(L-cystein-S-yl)-D-asparagine" EXACT RESID-alternate []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 7 H 9 N 3 O 3 S 1" xsd:string
-property_value: MassAvg "215.23" xsd:float
-property_value: MassMono "215.036462" xsd:float
-property_value: Origin "C, N" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00664
-is_a: MOD:02060
-is_a: MOD:01992
-
-[Term]
-id: MOD:01986
-name: 2-(L-cystein-S-yl)-L-serine
-def: "A protein modification that effectively cross-links an L-cysteine residue and an L-serine residue by a thioether bond to form 2-(S-L-cysteinyl)-L-serine." [PubMed:21526839, RESID:AA0623]
-comment: Cross-link 2.
-synonym: "(2R)-2-amino-2-([(2R)-2-amino-2-carboxyethyl]sulfanyl)-3-hydroxypropanoic acid" EXACT RESID-systematic []
-synonym: "(2R,5R)-2,5-diamino-5-carboxy-6-hydroxy-4-thiahexanoic acid" EXACT RESID-alternate []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 6 H 8 N 2 O 3 S 1" xsd:string
-property_value: MassAvg "188.20" xsd:float
-property_value: MassMono "188.025563" xsd:float
-property_value: Origin "C, S" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:02055
-is_a: MOD:01992
-
-[Term]
-id: MOD:01987
-name: 2-(L-cystein-S-yl)-D-serine
-def: "A protein modification that effectively cross-links an L-cysteine residue and an L-serine residue by a thioether bond to form 2-(S-L-cysteinyl)-D-serine." [PubMed:21786372, RESID:AA0624]
-comment: Cross-link 2.
-synonym: "(2R,5S)-2,5-diamino-5-carboxy-6-hydroxy-4-thiahexanoic acid" EXACT RESID-alternate []
-synonym: "(2S)-2-amino-2-([(2R)-2-amino-2-carboxyethyl]sulfanyl)-3-hydroxypropanoic acid" EXACT RESID-systematic []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 6 H 8 N 2 O 3 S 1" xsd:string
-property_value: MassAvg "188.20" xsd:float
-property_value: MassMono "188.025563" xsd:float
-property_value: Origin "C, S" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00664
-is_a: MOD:02064
-is_a: MOD:01992
-
-[Term]
-id: MOD:01988
-name: 2-(L-cystein-S-yl)-L-threonine
-def: "A protein modification that effectively cross-links an L-cysteine residue and an L-threonine residue by a thioether bond to form 2-(S-L-cysteinyl)-L-threonine." [PubMed:21526839, RESID:AA0625]
-comment: Cross-link 2.
-synonym: "(2R,3R)-2-amino-2-[(2R)-2-amino-2-carboxyethyl]sulfanyl-3-hydroxybutanoic acid" EXACT RESID-systematic []
-synonym: "(2R,5R,6R)-2,5-diamino-5-carboxy-6-hydroxy-4-thiaheptanoic acid" EXACT RESID-alternate []
-synonym: "alpha-(L-cystein-S-yl)-L-threonine" EXACT RESID-alternate []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 7 H 10 N 2 O 3 S 1" xsd:string
-property_value: MassAvg "202.23" xsd:float
-property_value: MassMono "202.041213" xsd:float
-property_value: Origin "C, T" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:02056
-is_a: MOD:01992
-
-[Term]
-id: MOD:01989
-name: 2-(L-cystein-S-yl)-D-tyrosine
-def: "A protein modification that effectively cross-links an L-cysteine residue and an L-tyrosine residue by a thioether bond to form 2-(S-L-cysteinyl)-D-tyrosine." [PubMed:21526839, RESID:AA0626]
-comment: Cross-link 2.
-synonym: "(2R,5S)-2,5-diamino-5-carboxyl-6-(hydroxyphenyl)-4-thiahexanoic acid" EXACT RESID-alternate []
-synonym: "(2S)-2-amino-2-([(2R)-2-amino-2-carboxyethyl]sulfanyl)-3-(4-hydroxyphenyl)propanoic acid" EXACT RESID-systematic []
-synonym: "alpha-(L-cystein-S-yl)-D-tyrosine" EXACT RESID-alternate []
-property_value: DiffAvg "-2.02" xsd:float
-property_value: DiffFormula "C 0 H -2 N 0 O 0 S 0" xsd:string
-property_value: DiffMono "-2.015650" xsd:float
-property_value: Formula "C 12 H 12 N 2 O 3 S 1" xsd:string
-property_value: MassAvg "264.30" xsd:float
-property_value: MassMono "264.056863" xsd:float
-property_value: Origin "C, Y" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00664
-is_a: MOD:02058
-is_a: MOD:01992
-
-[Term]
-id: MOD:01990
-name: protonated glycine (glycinium) residue
-def: "A protein modification that effectively converts a glycine residue to a glycinium (protonated glycine)." [ChEBI:64723, PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: DiffAvg "1.01" xsd:float
-property_value: DiffFormula "C 0 H 1 N 0 O 0" xsd:string
-property_value: DiffMono "1.007276" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 2 H 5 N 1 O 1" xsd:string
-property_value: MassAvg "59.07" xsd:float
-property_value: MassMono "59.036565" xsd:float
-property_value: Origin "G" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:00908
-is_a: MOD:01700
-
-[Term]
-id: MOD:01991
-name: N,N,N-trimethylglycine (from glycinium)
-def: "A protein modification that effectively converts a glycinium (protonated glycine) residue to an N,N,N-trimethylglycine." [ChEBI:17750, PubMed:23818633, PubMed:23978223, RESID:AA0619]
-comment: For amino acids residues, amine trimethylation can effectively only be accomplished with an aminium, protonated primary amino, group. This process accounts only for trimethylation and not protonation. The alternative N2Me3+Gly process (MOD:01982) accounts for both protonation and trimethylation.
-subset: PSI-MOD-slim
-synonym: "N2Me3Gly" EXACT PSI-MOD-label []
-property_value: DiffAvg "42.08" xsd:float
-property_value: DiffFormula "C 3 H 6 N 0 O 0" xsd:string
-property_value: DiffMono "42.046402" xsd:float
-property_value: FormalCharge "1+" xsd:string
-property_value: Formula "C 5 H 11 N 1 O 1" xsd:string
-property_value: MassAvg "101.15" xsd:float
-property_value: MassMono "101.083515" xsd:float
-property_value: Origin "MOD:01990" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:01687
-relationship: derives_from MOD:01990
-
-[Term]
-id: MOD:01992
-name: alpha-carbon thioether crosslinked residues
-def: "A protein modification that crosslinks two residues by formation of a thioether bond between a cysteine thiol and the alpha-carbon of another amino acid residue." [PubMed:18688235]
-is_a: MOD:00687
-
-[Term]
-id: MOD:01993
-name: beta-carbon thioether crosslinked residues
-def: "A protein modification that crosslinks two residues by formation of a thioether bond between a cysteine thiol and the beta-carbon of another amino acid residue." [PubMed:18688235]
-comment: These are typical lanthionine-like crosslinks.
-is_a: MOD:00687
-
-[Term]
-id: MOD:01994
-name: N1'-formyl-L-tryptophan
-def: "A protein modification that effectively converts an L-tryptophan residue to N1'-formyl-L-tryptophan." [PubMed:18688235]
-comment: This modifications has not been reported as commonly encountered [JSG].
-synonym: "N1'FoTrp" EXACT PSI-MOD-label []
-property_value: DiffAvg "28.01" xsd:float
-property_value: DiffFormula "C 1 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "27.994915" xsd:float
-property_value: Formula "C 12 H 10 N 2 O 2" xsd:string
-property_value: MassAvg "214.22" xsd:float
-property_value: MassMono "214.074228" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "hypothetical" xsd:string
-is_a: MOD:01106
-
-[Term]
-id: MOD:01995
-name: N2-formyl-L-tryptophan
-def: "A protein modification that effectively converts an L-tryptophan residue to N2-formyl-L-tryptophan." [PubMed:18688235]
-comment: This modifications has not been reported as commonly encountered [JSG].
-synonym: "N2FoTrp" EXACT PSI-MOD-label []
-property_value: DiffAvg "28.01" xsd:float
-property_value: DiffFormula "C 1 H 0 N 0 O 1" xsd:string
-property_value: DiffMono "27.994915" xsd:float
-property_value: Formula "C 12 H 11 N 2 O 2" xsd:string
-property_value: MassAvg "215.23" xsd:float
-property_value: MassMono "215.082053" xsd:float
-property_value: Origin "W" xsd:string
-property_value: Source "hypothetical" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:01106
-
-[Term]
-id: MOD:01996
-name: butanoylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with an butanoyl group." [PubMed:18688235]
-comment: Amino hydrogens are replaced to produce amides; hydroxyl hydrogens are replaced to produce esters; and hydrosulfanyl (thiol) hydrogens are replaced to produce sulfanyl esters (thiol esters).
-synonym: "ButRes" EXACT PSI-MOD-label []
-synonym: "Butyryl" RELATED Unimod-interim []
-synonym: "butyrylation" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "70.09" xsd:float
-property_value: DiffFormula "C 4 H 6 O 1" xsd:string
-property_value: DiffMono "70.041865" xsd:float
-property_value: Origin "X" xsd:string
-is_a: MOD:00649
-
-[Term]
-id: MOD:01997
-name: N-butanoylated residue
-def: "A protein modification that effectively replaces a residue amino or imino hydrogen with a butanoyl group." [PubMed:18688235]
-synonym: "N-butanoyl" EXACT PSI-MOD-alternate []
-synonym: "N-butanoylation" EXACT PSI-MOD-alternate []
-synonym: "N-butyryl" EXACT PSI-MOD-alternate []
-synonym: "N-butyrylation" EXACT PSI-MOD-alternate []
-synonym: "NButRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "70.09" xsd:float
-property_value: DiffFormula "C 4 H 6 N 0 O 1" xsd:string
-property_value: DiffMono "70.041865" xsd:float
-property_value: Origin "X" xsd:string
-is_a: MOD:01996
-
-[Term]
-id: MOD:01998
-name: alpha-amino butanoylated residue
-def: "A protein modification that effectively replaces a residue alpha-amino- or alpha-imino-hydrogen with a butanoyl group." [PubMed:18688235]
-synonym: "N2ButRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "70.09" xsd:float
-property_value: DiffFormula "C 4 H 6 N 0 O 1" xsd:string
-property_value: DiffMono "70.041865" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-property_value: TermSpec "N-term" xsd:string
-is_a: MOD:01997
-
-[Term]
-id: MOD:01999
-name: N6-(11-cis)-retinylidene-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-retinylidene-(11-cis)-L-lysine." [PubMed:18688235]
-synonym: "(2S)-2-amino-6-[(2E,4Z,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-en-1-yl)-2,4,6,8-nonatetraenylidene]aminohexanoic acid" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "266.43" xsd:float
-property_value: DiffFormula "C 20 H 26 N 0 O 0" xsd:string
-property_value: DiffMono "266.203451" xsd:float
-property_value: Formula "C 26 H 38 N 2 O 1" xsd:string
-property_value: MassAvg "394.60" xsd:float
-property_value: MassMono "394.298414" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:02000
-
-[Term]
-id: MOD:02000
-name: N6-retinylidene-L-lysine (unspecified geometric isomer)
-def: "A protein modification that effectively converts an L-lysine residue to N6-retinylidene-L-lysine (unspecified geometric isomer)." [PubMed:18688235]
-synonym: "(2S)-2-amino-6-[3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-en-1-yl)-2,4,6,8-nonatetraenylidene]aminohexanoic acid" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "266.43" xsd:float
-property_value: DiffFormula "C 20 H 26 N 0 O 0" xsd:string
-property_value: DiffMono "266.203451" xsd:float
-property_value: Formula "C 26 H 38 N 2 O 1" xsd:string
-property_value: MassAvg "394.60" xsd:float
-property_value: MassMono "394.298414" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00912
-
-[Term]
-id: MOD:02001
-name: stearoylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with a stearoyl group." []
-subset: PSI-MOD-slim
-property_value: DiffAvg "266.47" xsd:float
-property_value: DiffFormula "C 18 H 34 O 1" xsd:string
-property_value: DiffMono "266.260966" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00649
-is_a: MOD:01155
-
-[Term]
-id: MOD:02002
-name: S-palmitoleylated residue
-def: "A protein modification that effectively replaces a residue sulfanyl group with a palmitoleylsulfanyl group." []
-subset: PSI-MOD-slim
-property_value: DiffAvg "236.40" xsd:float
-property_value: DiffFormula "C 16 H 28 N 0 O 1" xsd:string
-property_value: DiffMono "236.214016" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00672
-is_a: MOD:01423
-
-[Term]
-id: MOD:02003
-name: O3-acylated L-serine
-def: "A protein modification that effectively replaces an O3-hydroxy hydrogen atom of L-serine with an acyl group." []
-subset: PSI-MOD-slim
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00671
-is_a: MOD:00916
-
-[Term]
-id: MOD:02004
-name: O3-acylated L-threonine
-def: "A protein modification that effectively replaces an O3-hydroxy hydrogen atom of L-threonine with an acyl group." []
-subset: PSI-MOD-slim
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00671
-is_a: MOD:00917
-
-[Term]
-id: MOD:02005
-name: S-acylated L-cysteine
-def: "A protein modification that effectively replaces an sulfanyl hydrogen atom of L-cysteine with an acyl group." []
-subset: PSI-MOD-slim
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00672
-is_a: MOD:00905
-
-[Term]
-id: MOD:02006
-name: S-stearoylated residue
-def: "A protein modification that effectively replaces a residue sulfanyl group with a stearoylsulfanyl group." []
-subset: PSI-MOD-slim
-property_value: DiffAvg "266.47" xsd:float
-property_value: DiffFormula "C 18 H 34 O 1" xsd:string
-property_value: DiffMono "266.260966" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00672
-is_a: MOD:02001
-
-[Term]
-id: MOD:02007
-name: N6-palmitoleyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-palmitoleyl-L-lysine." []
-subset: PSI-MOD-slim
-property_value: DiffAvg "236.40" xsd:float
-property_value: DiffFormula "C 16 H 28 N 0 O 1" xsd:string
-property_value: DiffMono "236.214016" xsd:float
-property_value: Formula "C 22 H 40 N 2 O 2" xsd:string
-property_value: MassAvg "364.58" xsd:float
-property_value: MassMono "364.308979" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:01875
-is_a: MOD:02008
-
-[Term]
-id: MOD:02008
-name: N-palmitoleylated residue
-def: "A protein modification that effectively replaces a residue amino group with a palmitoleylamino group." []
-subset: PSI-MOD-slim
-property_value: DiffAvg "236.40" xsd:float
-property_value: DiffFormula "C 16 H 28 N 0 O 1" xsd:string
-property_value: DiffMono "236.214016" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00670
-is_a: MOD:01423
-
-[Term]
-id: MOD:02009
-name: N6-stearoyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-stearoyl-L-lysine." []
-subset: PSI-MOD-slim
-property_value: DiffAvg "266.47" xsd:float
-property_value: DiffFormula "C 18 H 34 O 1" xsd:string
-property_value: DiffMono "266.260966" xsd:float
-property_value: Formula "C 24 H 46 N 2 O 2" xsd:string
-property_value: MassAvg "394.65" xsd:float
-property_value: MassMono "394.355929" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:01875
-is_a: MOD:02010
-
-[Term]
-id: MOD:02010
-name: N-stearoylated residue
-def: "A protein modification that effectively replaces a residue amino group with a stearoylamino group." []
-subset: PSI-MOD-slim
-property_value: DiffAvg "266.47" xsd:float
-property_value: DiffFormula "C 18 H 34 O 1" xsd:string
-property_value: DiffMono "266.260966" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00670
-is_a: MOD:02001
-
-[Term]
-id: MOD:02011
-name: N-oleoylated residue
-def: "A protein modification that effectively replaces a residue amino group with a oleoylamino group." []
-subset: PSI-MOD-slim
-property_value: DiffAvg "264.45" xsd:float
-property_value: DiffFormula "C 18 H 32 N 0 O 1" xsd:string
-property_value: DiffMono "264.245316" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00670
-is_a: MOD:02012
-
-[Term]
-id: MOD:02012
-name: oleoylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with a oleoyl group." []
-subset: PSI-MOD-slim
-property_value: DiffAvg "264.45" xsd:float
-property_value: DiffFormula "C 18 H 32 N 0 O 1" xsd:string
-property_value: DiffMono "264.245316" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00649
-is_a: MOD:01155
-
-[Term]
-id: MOD:02013
-name: N6-linoloyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-linoloyl-L-lysine." []
-subset: PSI-MOD-slim
-property_value: DiffAvg "262.45" xsd:float
-property_value: DiffFormula "C 18 H 30 N 0 O 1" xsd:string
-property_value: DiffMono "262.229666" xsd:float
-property_value: Formula "C 24 H 42 N 2 O 2" xsd:string
-property_value: MassAvg "390.63" xsd:float
-property_value: MassMono "390.324629" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:01875
-is_a: MOD:02014
-
-[Term]
-id: MOD:02014
-name: N-linoloylated residue
-def: "A protein modification that effectively replaces a residue amino group with a linoloylamino group." []
-subset: PSI-MOD-slim
-property_value: DiffAvg "262.45" xsd:float
-property_value: DiffFormula "C 18 H 30 N 0 O 1" xsd:string
-property_value: DiffMono "262.229666" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00670
-is_a: MOD:02015
-
-[Term]
-id: MOD:02015
-name: linoloylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with a linoloyl group." []
-subset: PSI-MOD-slim
-property_value: DiffAvg "262.45" xsd:float
-property_value: DiffFormula "C 18 H 30 N 0 O 1" xsd:string
-property_value: DiffMono "262.229666" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00649
-is_a: MOD:01155
-
-[Term]
-id: MOD:02016
-name: N6-arachidonoyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-arachidonoyl-L-lysine." []
-subset: PSI-MOD-slim
-property_value: DiffAvg "286.49" xsd:float
-property_value: DiffFormula "C 20 H 30 N 0 O 1" xsd:string
-property_value: DiffMono "286.229666" xsd:float
-property_value: Formula "C 26 H 42 N 2 O 2" xsd:string
-property_value: MassAvg "414.67" xsd:float
-property_value: MassMono "414.324629" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:01875
-is_a: MOD:02017
-
-[Term]
-id: MOD:02017
-name: N-arachidonoylated residue
-def: "A protein modification that effectively replaces a residue amino group with an arachidonoylamino group." []
-subset: PSI-MOD-slim
-property_value: DiffAvg "286.49" xsd:float
-property_value: DiffFormula "C 20 H 30 N 0 O 1" xsd:string
-property_value: DiffMono "286.229666" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00670
-is_a: MOD:02018
-
-[Term]
-id: MOD:02018
-name: arachidonoylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with an arachidonoyl group." []
-subset: PSI-MOD-slim
-property_value: DiffAvg "286.49" xsd:float
-property_value: DiffFormula "C 20 H 30 N 0 O 1" xsd:string
-property_value: DiffMono "286.229666" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00649
-is_a: MOD:01155
-
-[Term]
-id: MOD:02019
-name: N6-timnodonoyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-timnodonoyl-L-lysine." []
-subset: PSI-MOD-slim
-property_value: DiffAvg "284.48" xsd:float
-property_value: DiffFormula "C 20 H 28 N 0 O 1" xsd:string
-property_value: DiffMono "284.214016" xsd:float
-property_value: Formula "C 26 H 40 N 2 O 2" xsd:string
-property_value: MassAvg "412.66" xsd:float
-property_value: MassMono "412.308979" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:01875
-is_a: MOD:02020
-
-[Term]
-id: MOD:02020
-name: N-timnodonoylated residue
-def: "A protein modification that effectively replaces a residue amino group with a timnodonoylamino group." []
-subset: PSI-MOD-slim
-property_value: DiffAvg "284.48" xsd:float
-property_value: DiffFormula "C 20 H 28 N 0 O 1" xsd:string
-property_value: DiffMono "284.214016" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00670
-is_a: MOD:02021
-
-[Term]
-id: MOD:02021
-name: timnodonoylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with a timnodonoyl group." []
-subset: PSI-MOD-slim
-property_value: DiffAvg "284.48" xsd:float
-property_value: DiffFormula "C 20 H 28 N 0 O 1" xsd:string
-property_value: DiffMono "284.214016" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00649
-is_a: MOD:01155
-
-[Term]
-id: MOD:02022
-name: N6-cervonoyl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-cervonoyl-L-lysine." []
-subset: PSI-MOD-slim
-property_value: DiffAvg "310.53" xsd:float
-property_value: DiffFormula "C 22 H 30 N 0 O 1" xsd:string
-property_value: DiffMono "310.229666" xsd:float
-property_value: Formula "C 28 H 42 N 2 O 2" xsd:string
-property_value: MassAvg "438.71" xsd:float
-property_value: MassMono "438.324629" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:01875
-is_a: MOD:02023
-
-[Term]
-id: MOD:02023
-name: N-cervonoylated residue
-def: "A protein modification that effectively replaces a residue amino group with a cervonoylamino group." []
-subset: PSI-MOD-slim
-property_value: DiffAvg "310.53" xsd:float
-property_value: DiffFormula "C 22 H 30 N 0 O 1" xsd:string
-property_value: DiffMono "310.229666" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00670
-is_a: MOD:02024
-
-[Term]
-id: MOD:02024
-name: cervonoylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with a cervonoyl group." []
-subset: PSI-MOD-slim
-property_value: DiffAvg "310.53" xsd:float
-property_value: DiffFormula "C 22 H 30 N 0 O 1" xsd:string
-property_value: DiffMono "310.229666" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00649
-is_a: MOD:01155
-
-[Term]
-id: MOD:02025
-name: 5-glutaminyl glutamic acid
-def: "A protein modification that effectively converts the alpha amino group of a glutamine residue to glutaminyl glutamic acid by forming an isopeptide bond with the side chain carboxyl group of a free glutamic acid." [PubMed:28801462]
-property_value: DiffAvg "128.13" xsd:float
-property_value: DiffFormula "C 5 H 8 N 2 O 2" xsd:string
-property_value: DiffMono "128.058576" xsd:float
-property_value: Formula "C 10 H 15 N 3 O 5" xsd:string
-property_value: MassAvg "257.24" xsd:float
-property_value: MassMono "257.101167" xsd:float
-property_value: Origin "E" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00906
-
-[Term]
-id: MOD:02026
-name: S-(cysteinyl-glycyl)-L-cysteine
-def: "A protein modification that effectively cross-links an L-cysteinyl-L-glycine dipeptide and an L-cysteine residue by a disulfide bond to form S-(cysteinyl-glycyl)-L-cysteine." [PubMed:27936627, PubMed:20594348, PubMed:29627744]
-comment: Glutamyl-transpeptidase cleaves glutathione into cysteinylglycine (Cys-Gly) and a Glu residue. [PubMed:28537416]
-property_value: DiffAvg "176.17" xsd:float
-property_value: DiffFormula "C 5 H 8 N 2 O 3 S 1" xsd:string
-property_value: DiffMono "176.025563" xsd:float
-property_value: Formula "C 8 H 13 N 3 O 4 S 2" xsd:string
-property_value: MassAvg "279.33" xsd:float
-property_value: MassMono "279.034748" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00905
-is_a: MOD:01862
-relationship: part_of MOD:00234
-
-[Term]
-id: MOD:02027
-name: urmylated lysine
-def: "A protein modification that effectively crosslinks the N6-amino of a peptidyl lysine with the carboxyl-terminal glycine of a URM1 protein." [PubMed:10713047, PubMed:21209336]
-subset: PSI-MOD-slim
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:02047
-is_a: MOD:02051
-is_a: MOD:01875
-relationship: contains MOD:00134
-
-[Term]
-id: MOD:02028
-name: iTRAQ4plex reporter+balance reagent acylated residue, average mass modification
-def: "A protein modification that effectively replaces a hydrogen atom of a residue with one of the Applied Biosystems iTRAQ4plex reagent reporter+balance groups." [Unimod:214]
-comment: The reagent consists of a reporter group, a balance group and a protein reactive N-oxysuccinimide group. The reporter group, an isotopically labeled 1,4-dimethylpiperazine, is connected to a carbonyl balance group that is isotopically labeled to produce a nominally isobaric combined modification. Four versions of chemically identical iTRAQ4plex moyeties, but with different isotope distribution. This modification is calculated as the average of the four species. It has no isotopic distribution reality, the exact mass does not correspond to any real isotopic distribution.
-subset: PSI-MOD-slim
-synonym: "(4-methylpiperazin-1-yl)acetyl" EXACT PSI-MOD-alternate []
-synonym: "iTRAQ" RELATED Unimod-interim []
-property_value: DiffAvg "144.10" xsd:float
-property_value: DiffMono "144.102411" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:01426
-is_a: MOD:01705
-is_a: MOD:01709
-is_a: MOD:01513
-
-[Term]
-id: MOD:02029
-name: cis-peptidyl-L-proline
-def: "A protein modification that effectively specifies the boundary conformation of two adjacent source amino acid residues, the second (C-term side) being a L-proline, where the carbonyl group of the amide bond of the N-side of the L-proline is positioned such that the organodiyl group is in the cis orientation (omega=0)" [ChEBI:83833, PubMed:15735342, PubMed:15311922, PubMed:24116866, PubMed:5485910]
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Origin "X, P" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00915
-
-[Term]
-id: MOD:02030
-name: trans-peptidyl-L-proline
-def: "A protein modification that effectively specifies the boundary conformation of two adjacent source amino acid residues, the second (C-term side) being a L-proline, where the carbonyl group of the amide bond of the N-side of the L-proline is positioned such that the organodiyl group is in the trans orientation (omega=180)" [ChEBI:83834, PubMed:15735342, PubMed:15311922, PubMed:24116866, PubMed:5485910]
-property_value: DiffAvg "0.00" xsd:float
-property_value: DiffFormula "C 0 H 0 N 0 O 0" xsd:string
-property_value: DiffMono "0.000000" xsd:float
-property_value: Origin "X, P" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00915
-
-[Term]
-id: MOD:02031
-name: dHex1Hex4HexNAc5 N4-glycosylated asparagine
-def: "modification from Unimod N-linked glycosylation, dHex Hex(4) HexNAc(5)" [PubMed:33135055, Unimod:1519]
-synonym: "dHex Hex(4) HexNAc(5)" RELATED Unimod-description []
-property_value: DiffAvg "1810.68" xsd:float
-property_value: DiffFormula "C 70 H 115 N 5 O 49" xsd:string
-property_value: DiffMono "1809.666065" xsd:float
-property_value: Formula "C 74 H 121 N 7 O 51" xsd:string
-property_value: MassAvg "1924.78" xsd:float
-property_value: MassMono "1923.708993" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:1519
-xref: GNO:G03382KH
-is_a: MOD:00725
-is_a: MOD:00160
-
-[Term]
-id: MOD:02032
-name: dHex2Hex4HexNAc5 N4-glycosylated asparagine
-def: "modification from Unimod N-linked glycosylation, dHex(2) Hex(4) HexNAc(5)" [PubMed:33135055, Unimod:1785]
-synonym: "dHex(2) Hex(4) HexNAc(5)" RELATED Unimod-description []
-property_value: DiffAvg "1956.82" xsd:float
-property_value: DiffFormula "C 76 H 125 N 5 O 53" xsd:string
-property_value: DiffMono "1955.723974" xsd:float
-property_value: Formula "C 80 H 131 N 7 O 55" xsd:string
-property_value: MassAvg "2070.92" xsd:float
-property_value: MassMono "2069.766901" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:1785
-xref: GNO:G70418MS
-is_a: MOD:00725
-is_a: MOD:00160
-
-[Term]
-id: MOD:02033
-name: dHex1Hex5HexNAc3 N4-glycosylated asparagine
-def: "modification from Unimod N-linked glycosylation, dHex Hex(5) HexNAc(3)" [PubMed:33135055, Unimod:1484]
-synonym: "dHex Hex(5) HexNAc(3)" RELATED Unimod-description []
-property_value: DiffAvg "1566.43" xsd:float
-property_value: DiffFormula "C 60 H 99 N 3 O 44" xsd:string
-property_value: DiffMono "1565.560143" xsd:float
-property_value: Formula "C 64 H 105 N 5 O 46" xsd:string
-property_value: MassAvg "1680.53" xsd:float
-property_value: MassMono "1679.603071" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:1484
-xref: GNO:G82119TF
-is_a: MOD:00725
-is_a: MOD:00160
-
-[Term]
-id: MOD:02034
-name: dHex1Hex3HexNAc6 N4-glycosylated asparagine
-def: "modification from Unimod N-linked glycosylation, dHex Hex(3) HexNAc(6)" [PubMed:33135055, Unimod:1781]
-synonym: "dHex Hex(3) HexNAc(6)" RELATED Unimod-description []
-property_value: DiffAvg "1851.73" xsd:float
-property_value: DiffFormula "C 72 H 118 N 6 O 49" xsd:string
-property_value: DiffMono "1850.692614" xsd:float
-property_value: Formula "C 76 H 124 N 8 O 51" xsd:string
-property_value: MassAvg "1965.83" xsd:float
-property_value: MassMono "1964.735542" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:1781
-xref: GNO:G50757KG
-is_a: MOD:00725
-is_a: MOD:00160
-
-[Term]
-id: MOD:02035
-name: dHex1Hex6HexNAc3 N4-glycosylated asparagine
-def: "modification from Unimod N-linked glycosylation, dHex Hex(6) HexNAc(3)" [PubMed:33135055, Unimod:1509]
-synonym: "dHex Hex(6) HexNAc(3)" RELATED Unimod-description []
-property_value: DiffAvg "1728.57" xsd:float
-property_value: DiffFormula "C 66 H 109 N 3 O 49" xsd:string
-property_value: DiffMono "1727.612967" xsd:float
-property_value: Formula "C 70 H 115 N 5 O 51" xsd:string
-property_value: MassAvg "1842.67" xsd:float
-property_value: MassMono "1841.655894" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:1509
-xref: GNO:G84820NF
-is_a: MOD:00725
-is_a: MOD:00160
-
-[Term]
-id: MOD:02036
-name: Hex9HexNAc2 N4-glycosylated asparagine
-def: "modification from Unimod N-linked glycosylation, Hex(9)HexNAc(2)" [PubMed:33135055, Unimod:1531]
-synonym: "M9/Man9" RELATED Unimod-description []
-property_value: DiffAvg "1865.66" xsd:float
-property_value: DiffFormula "C 70 H 116 N 2 O 55" xsd:string
-property_value: DiffMono "1864.634156" xsd:float
-property_value: Formula "C 74 H 122 N 4 O 57" xsd:string
-property_value: MassAvg "1979.76" xsd:float
-property_value: MassMono "1978.677083" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:1531
-xref: GNO:G70101JE
-is_a: MOD:00725
-is_a: MOD:00160
-
-[Term]
-id: MOD:02037
-name: Hex7HexNAc2 N4-glycosylated asparagine
-def: "modification from Unimod N-linked glycosylation, Hex(7) HexNAc(2)" [PubMed:33135055, Unimod:1480]
-synonym: "M7/Man7" RELATED Unimod-description []
-property_value: DiffAvg "1541.38" xsd:float
-property_value: DiffFormula "C 58 H 96 N 2 O 45" xsd:string
-property_value: DiffMono "1540.528509" xsd:float
-property_value: Formula "C 62 H 102 N 4 O 47" xsd:string
-property_value: MassAvg "1655.48" xsd:float
-property_value: MassMono "1654.571436" xsd:float
-property_value: MassMono "1654.571436" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:1480
-xref: GNO:G05724UK
-is_a: MOD:00725
-is_a: MOD:00160
-
-[Term]
-id: MOD:02038
-name: monomethylated L-histidine
-def: "A protein modification that effectively replaces one hydrogen atom of an L-histidine residue with one methyl group." [DeltaMass:215, OMSSA:77, Unimod:34#H]
-subset: PSI-MOD-slim
-synonym: "Me1His" EXACT PSI-MOD-label []
-synonym: "Methyl" RELATED PSI-MS-label []
-synonym: "methylh" EXACT OMSSA-label []
-synonym: "MOD_RES Methylhistidine" EXACT UniProt-feature []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 7 H 9 N 3 O 1" xsd:string
-property_value: MassAvg "151.17" xsd:float
-property_value: MassMono "151.074562" xsd:float
-property_value: Origin "H" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:34
-xref: uniprot.ptm:PTM-0176
-is_a: MOD:00599
-is_a: MOD:00661
-
-[Term]
-id: MOD:02039
-name: aminated residue
-def: "A protein modification that effectively replaces a hydrogen group with a amino group" []
-synonym: "AmRes" EXACT PSI-MOD-label []
-property_value: Origin "X" xsd:string
-is_a: MOD:01156
-
-[Term]
-id: MOD:02040
-name: crosslinked L-alanine residue
-def: "A protein modification that contains an L-alanine residue crosslinked to one or more amino acid residues." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "XlnkAla" EXACT PSI-MOD-label []
-property_value: Origin "A" xsd:string
-is_a: MOD:00901
-
-[Term]
-id: MOD:02041
-name: crosslinked L-arginine residue
-def: "A protein modification that contains an L-arginine residue crosslinked to one or more amino acid residues." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "XlnkArg" EXACT PSI-MOD-label []
-property_value: Origin "R" xsd:string
-is_a: MOD:00902
-
-[Term]
-id: MOD:02042
-name: crosslinked L-asparagine residue
-def: "A protein modification that contains an L-asparagine residue crosslinked to one or more amino acid residues." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "XlnkAsn" EXACT PSI-MOD-label []
-property_value: Origin "N" xsd:string
-is_a: MOD:00903
-
-[Term]
-id: MOD:02043
-name: crosslinked L-aspartic acid residue
-def: "A protein modification that contains an L-aspartic acid residue crosslinked to one or more amino acid residues." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "XlnkAsp" EXACT PSI-MOD-label []
-property_value: Origin "D" xsd:string
-is_a: MOD:00904
-
-[Term]
-id: MOD:02044
-name: crosslinked L-cysteine residue
-def: "A protein modification that contains an L-cysteine residue crosslinked to one or more amino acid residues." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "XlnkCys" EXACT PSI-MOD-label []
-property_value: Origin "C" xsd:string
-is_a: MOD:00905
-
-[Term]
-id: MOD:02045
-name: crosslinked L-glutamic acid residue
-def: "A protein modification that contains an L-glutamic acid residue crosslinked to one or more amino acid residues." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "XlnkGlu" EXACT PSI-MOD-label []
-property_value: Origin "E" xsd:string
-is_a: MOD:00906
-
-[Term]
-id: MOD:02046
-name: crosslinked L-glutamine residue
-def: "A protein modification that contains an L-glutamine residue crosslinked to one or more amino acid residues." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "XlnkGln" EXACT PSI-MOD-label []
-property_value: Origin "Q" xsd:string
-is_a: MOD:00907
-
-[Term]
-id: MOD:02047
-name: crosslinked glycine residue
-def: "A protein modification that contains a glycine residue crosslinked to one or more amino acid residues." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "XlnkGly" EXACT PSI-MOD-label []
-property_value: Origin "G" xsd:string
-is_a: MOD:00908
-
-[Term]
-id: MOD:02048
-name: crosslinked L-histidine residue
-def: "A protein modification that contains an L-histidine residue crosslinked to one or more amino acid residues." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "XlnkHis" EXACT PSI-MOD-label []
-property_value: Origin "H" xsd:string
-is_a: MOD:00909
-
-[Term]
-id: MOD:02049
-name: crosslinked L-isoleucine residue
-def: "A protein modification that contains an L-isoleucine residue crosslinked to one or more amino acid residues." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "XlnkIle" EXACT PSI-MOD-label []
-property_value: Origin "I" xsd:string
-is_a: MOD:00910
-
-[Term]
-id: MOD:02050
-name: crosslinked L-leucine residue
-def: "A protein modification that contains an L-leucine residue crosslinked to one or more amino acid residues." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "XlnkLeu" EXACT PSI-MOD-label []
-property_value: Origin "L" xsd:string
-is_a: MOD:00911
-
-[Term]
-id: MOD:02051
-name: crosslinked L-lysine residue
-def: "A protein modification that contains an L-lysine residue crosslinked to one or more amino acid residues." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "XlnkLys" EXACT PSI-MOD-label []
-property_value: Origin "K" xsd:string
-is_a: MOD:00912
-
-[Term]
-id: MOD:02052
-name: crosslinked L-methionine residue
-def: "A protein modification that contains an L-methionine residue crosslinked to one or more amino acid residues." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "XlnkMet" EXACT PSI-MOD-label []
-property_value: Origin "M" xsd:string
-is_a: MOD:00913
-
-[Term]
-id: MOD:02053
-name: crosslinked L-phenylalanine residue
-def: "A protein modification that contains an L-phenylalanine residue crosslinked to one or more amino acid residues." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "XlnkPhe" EXACT PSI-MOD-label []
-property_value: Origin "F" xsd:string
-is_a: MOD:00914
-
-[Term]
-id: MOD:02054
-name: crosslinked L-proline residue
-def: "A protein modification that contains an L-proline residue crosslinked to one or more amino acid residues." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "XlnkPro" EXACT PSI-MOD-label []
-property_value: Origin "P" xsd:string
-is_a: MOD:00915
-
-[Term]
-id: MOD:02055
-name: crosslinked L-serine residue
-def: "A protein modification that contains an L-serine residue crosslinked to one or more amino acid residues." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "XlnkSer" EXACT PSI-MOD-label []
-property_value: Origin "S" xsd:string
-is_a: MOD:00916
-
-[Term]
-id: MOD:02056
-name: crosslinked L-threonine residue
-def: "A protein modification that contains an L-threonine residue crosslinked to one or more amino acid residues." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "XlnkThr" EXACT PSI-MOD-label []
-property_value: Origin "T" xsd:string
-is_a: MOD:00917
-
-[Term]
-id: MOD:02057
-name: crosslinked L-tryptophan residue
-def: "A protein modification that contains an L-tryptophan residue crosslinked to one or more amino acid residues." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "XlnkTrp" EXACT PSI-MOD-label []
-property_value: Origin "W" xsd:string
-is_a: MOD:00918
-
-[Term]
-id: MOD:02058
-name: crosslinked L-tyrosine residue
-def: "A protein modification that contains an L-tyrosine residue crosslinked to one or more amino acid residues." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "XlnkTyr" EXACT PSI-MOD-label []
-property_value: Origin "Y" xsd:string
-is_a: MOD:00919
-
-[Term]
-id: MOD:02059
-name: crosslinked L-valine residue
-def: "A protein modification that contains an L-valine residue crosslinked to one or more amino acid residues." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "XlnkVal" EXACT PSI-MOD-label []
-property_value: Origin "V" xsd:string
-is_a: MOD:00920
-
-[Term]
-id: MOD:02060
-name: crosslinked D-asparagine residue
-def: "A protein modification that contains an D-asparagine residue crosslinked to one or more amino acid residues." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "XlnkDAsn" EXACT PSI-MOD-label []
-property_value: Origin "MOD:00203" xsd:string
-is_a: MOD:02097
-
-[Term]
-id: MOD:02061
-name: crosslinked L-selenocysteine residue
-def: "A protein modification that contains an L-selenocysteine residue crosslinked to one or more amino acid residues." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: Origin "U" xsd:string
-is_a: MOD:01158
-
-[Term]
-id: MOD:02062
-name: crosslinked N-formyl-L-methionine residue
-def: "A protein modification that contains an N-formyl-L-methionine residue crosslinked to one or more amino acid residues." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: Origin "MOD:00030" xsd:string
-is_a: MOD:01450
-
-[Term]
-id: MOD:02063
-name: crosslinked D-phenylalanine residue
-def: "A protein modification that contains an D-phenylalanine residue crosslinked to one or more amino acid residues." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "XlnkDPhe" EXACT PSI-MOD-label []
-property_value: Origin "F" xsd:string
-is_a: MOD:00201
-
-[Term]
-id: MOD:02064
-name: crosslinked D-serine residue
-def: "A protein modification that contains an D-serine residue crosslinked to one or more amino acid residues." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "XlnkDSer" EXACT PSI-MOD-label []
-property_value: Origin "S" xsd:string
-is_a: MOD:00202
-
-[Term]
-id: MOD:02065
-name: metal or metal cluster coordinated L-alanine residue
-def: "A protein modification that contains an L-alanine residue coordinated to one or more metal atoms or metal clusters." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: Origin "A" xsd:string
-is_a: MOD:00901
-
-[Term]
-id: MOD:02066
-name: metal or metal cluster coordinated L-aspartic acid residue
-def: "A protein modification that contains an L-aspartic acid residue coordinated to one or more metal atoms or metal clusters." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: Origin "D" xsd:string
-is_a: MOD:00904
-
-[Term]
-id: MOD:02067
-name: metal or metal cluster coordinated L-cysteine residue
-def: "A protein modification that contains an L-cysteine residue coordinated to one or more metal atoms or metal clusters." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: Origin "C" xsd:string
-is_a: MOD:00905
-
-[Term]
-id: MOD:02068
-name: metal or metal cluster coordinated L-glutamic acid residue
-def: "A protein modification that contains an L-glutamic acid residue coordinated to one or more metal atoms or metal clusters." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: Origin "E" xsd:string
-is_a: MOD:00906
-
-[Term]
-id: MOD:02069
-name: metal or metal cluster coordinated L-glutamine residue
-def: "A protein modification that contains an L-glutamine residue coordinated to one or more metal atoms or metal clusters." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: Origin "Q" xsd:string
-is_a: MOD:00907
-
-[Term]
-id: MOD:02070
-name: metal or metal cluster coordinated L-histidine residue
-def: "A protein modification that contains an L-histidine residue coordinated to one or more metal atoms or metal clusters." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: Origin "H" xsd:string
-is_a: MOD:00909
-
-[Term]
-id: MOD:02071
-name: metal or metal cluster coordinated L-methionine residue
-def: "A protein modification that contains an L-methionine residue coordinated to one or more metal atoms or metal clusters." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: Origin "M" xsd:string
-is_a: MOD:00913
-
-[Term]
-id: MOD:02072
-name: metal or metal cluster coordinated L-serine residue
-def: "A protein modification that contains an L-serine residue coordinated to one or more metal atoms or metal clusters." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: Origin "S" xsd:string
-is_a: MOD:00916
-
-[Term]
-id: MOD:02073
-name: metal or metal cluster coordinated L-selenocysteine residue
-def: "A protein modification that contains an L-selenocysteine residue coordinated to one or more metal atoms or metal clusters." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: Origin "U" xsd:string
-is_a: MOD:01158
-
-[Term]
-id: MOD:02074
-name: metal or metal cluster coordinated L-lysine residue
-def: "A protein modification that contains an L-lysine residue coordinated to one or more metal atoms or metal clusters." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: Origin "K" xsd:string
-is_a: MOD:00912
-
-[Term]
-id: MOD:02075
-name: metal or metal cluster coordinated L-tyrosine residue
-def: "A protein modification that contains an L-tyrosine residue coordinated to one or more metal atoms or metal clusters." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: Origin "Y" xsd:string
-is_a: MOD:00919
-
-[Term]
-id: MOD:02076
-name: metal or metal cluster coordinated L-arginine residue
-def: "A protein modification that contains an L-arginine residue coordinated to one or more metal atoms or metal clusters." [PubMed:18688235]
-subset: PSI-MOD-slim
-property_value: Origin "R" xsd:string
-is_a: MOD:00902
-
-[Term]
-id: MOD:02077
-name: nitrosylated residue
-def: "A protein modification that effectively replaces a hydrogen atom with an nitrosyl (NO) group." [PubMed:10442087, PubMed:11562475, PubMed:15688001, PubMed:8626764, PubMed:8637569, Unimod:275]
-subset: PSI-MOD-slim
-synonym: "Nitrosyl" RELATED PSI-MS-label []
-property_value: DiffAvg "29.00" xsd:float
-property_value: DiffFormula "C 0 H -1 N 1 O 1 S 0" xsd:string
-property_value: DiffMono "28.990164" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:275
-is_a: MOD:01156
-
-[Term]
-id: MOD:02078
-name: acetylated residue
-def: "A protein modification that effectively replaces one or more hydrogen atoms with one or more acetyl groups." [PubMed:11857757, PubMed:11999733, PubMed:12175151, PubMed:14730666, PubMed:15350136]
-subset: PSI-MOD-slim
-synonym: "Acetyl" RELATED PSI-MS-label []
-synonym: "AcRes" EXACT PSI-MOD-label []
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:00649
-
-[Term]
-id: MOD:02079
-name: diacetylated residue
-def: "A protein modification that effectively replaces one hydrogen atom with one acetyl group." [PubMed:11857757, PubMed:11999733, PubMed:12175151, PubMed:14730666, PubMed:15350136, Unimod:1]
-comment: Amino hydrogens are replaced to produce amides; hydroxyl hydrogens are replaced to produce esters; and hydrosulfanyl (thiol) hydrogens are replaced to produce sulfanyl esters (thiol esters). From DeltaMass: Average Mass: 42
-subset: PSI-MOD-slim
-synonym: "Diacetyl" RELATED PSI-MS-label []
-synonym: "Ac2Res" EXACT PSI-MOD-label []
-property_value: DiffAvg "84.07" xsd:float
-property_value: DiffFormula "C 4 H 4 N 0 O 2" xsd:string
-property_value: DiffMono "84.021129" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "artifact" xsd:string
-is_a: MOD:02078
-
-[Term]
-id: MOD:02080
-name: diacetylated L-serine
-def: "A protein modification that effectively converts an L-serine residue to either N-acetyl-L-serine, O-acetyl-L-serine, or N,O-diacetyl-L-serine." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "Ac2Ser" EXACT PSI-MOD-label []
-property_value: DiffAvg "84.07" xsd:float
-property_value: DiffFormula "C 4 H 4 N 0 O 2" xsd:string
-property_value: DiffMono "84.021129" xsd:float
-property_value: Formula "C 7 H 10 N 1 O 4" xsd:string
-property_value: MassAvg "172.16" xsd:float
-property_value: MassMono "172.060983" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:02079
-is_a: MOD:00916
-
-[Term]
-id: MOD:02081
-name: alpha-amino succinylated residue
-def: "A protein modification that effectively replaces a residue alpha-amino- or alpha-imino-hydrogen with a succinyl group." [PubMed:11857757, PubMed:12175151, Unimod:64#N-term]
-synonym: "Succinyl" RELATED PSI-MS-label []
-property_value: DiffAvg "100.07" xsd:float
-property_value: DiffFormula "C 4 H 4 O 3" xsd:string
-property_value: DiffMono "100.016044" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-property_value: TermSpec "N-term" xsd:string
-xref: Unimod:64
-is_a: MOD:01029
-is_a: MOD:01696
-is_a: MOD:01426
-
-[Term]
-id: MOD:02082
-name: didehydrogenated and dehydrated residue
-def: "A protein modification that effectively removes two neutral hydrogen atoms (proton and electron) and a water moiety from a residue." [Unimod:401]
-subset: PSI-MOD-slim
-synonym: "2dHdH2ORes" EXACT PSI-MOD-label []
-property_value: DiffAvg "-20.03" xsd:float
-property_value: DiffFormula "C 0 H -4 N 0 O -1" xsd:string
-property_value: DiffMono "-20.026215" xsd:float
-property_value: Origin "X" xsd:string
-is_a: MOD:00683
-
-[Term]
-id: MOD:02083
-name: 4alpha-FMN modified residue
-def: "A protein modification that effectively results from forming an adduct with a compound containing a riboflavin phosphate (flavin mononucleotide, FMN) group through the 4-alpha position of FMN." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "4aFMNRes" EXACT PSI-MOD-label []
-property_value: DiffFormula "C 17 H 21 N 4 O 9 P 1" xsd:string
-property_value: DiffAvg "456.35" xsd:float
-property_value: DiffMono "456.104615" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00896
-
-[Term]
-id: MOD:02084
-name: 6-FMN modified residue
-def: "A protein modification that effectively results from forming an adduct with a compound containing a riboflavin phosphate (flavin mononucleotide, FMN) group through the 6 position of FMN." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "6-FMNRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "454.33" xsd:float
-property_value: DiffFormula "C 17 H 19 N 4 O 9 P 1" xsd:string
-property_value: DiffMono "454.088965" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00896
-
-[Term]
-id: MOD:02085
-name: 8alpha-FMN modified residue
-def: "A protein modification that effectively results from forming an adduct with a compound containing a riboflavin phosphate (flavin mononucleotide, FMN) group through the 8-alpha position of FMN." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "8a-FMNRes" EXACT PSI-MOD-label []
-property_value: DiffAvg "454.33" xsd:float
-property_value: DiffFormula "C 17 H 19 N 4 O 9 P 1" xsd:string
-property_value: DiffMono "454.088965" xsd:float
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00896
-
-[Term]
-id: MOD:02086
-name: brominated phenylalanine
-def: "A protein modification that effectively substitutes a hydrogen atom of an L-phenylalanine residue with a bromine atom." [PubMed:18688235]
-synonym: "BrPhe" EXACT PSI-MOD-label []
-property_value: Origin "F" xsd:string
-is_a: MOD:00754
-is_a: MOD:01066
-
-[Term]
-id: MOD:02087
-name: adenosine diphosphoribosyl (ADP-ribosyl) modified residue
-def: "A protein modification that effectively results from forming an adduct with one or more ADP-ribose moieties or to modified residues through formation of a glycosidic bond." [DeltaMass:0]
-subset: PSI-MOD-slim
-synonym: "ADPRibRes" EXACT PSI-MOD-label []
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00701
-
-[Term]
-id: MOD:02088
-name: natural, standard, encoded residue substitution
-def: "A protein modification that effectively replaces a natural, standard, encoded residue." [PubMed:18688235]
-comment: This represents the replacement of an encoded residue in a polypeptide, and must be combined with the formula or mass of another entry that is the replacement residue to represent a mutation or substitution.
-subset: PSI-MOD-slim
-property_value: Origin "X" xsd:string
-property_value: Source "natural" xsd:string
-is_a: MOD:00009
-is_a: MOD:01156
-
-[Term]
-id: MOD:02089
-name: O-(phospho-5'-uridine)-L-serine
-def: "A protein modification that effectively crosslinks an L-serine residue and 5'-phosphouridine through a phosphodiester bond to form O-(phospho-5'-uridine)-L-serine." [DeltaMass:0, PubMed:22504181, Unimod:417#S, ChEBI:156051]
-subset: PSI-MOD-slim
-synonym: "MOD_RES O-UMP-serine" EXACT UniProt-feature []
-synonym: "OUMPSer" EXACT PSI-MOD-label []
-synonym: "PhosphoUridine" RELATED PSI-MS-label []
-property_value: DiffAvg "306.17" xsd:float
-property_value: DiffFormula "C 9 H 11 N 2 O 8 P 1" xsd:string
-property_value: DiffMono "306.025302" xsd:float
-property_value: Formula "C 12 H 16 N 3 O 9 P 1" xsd:string
-property_value: MassAvg "377.24" xsd:float
-property_value: MassMono "377.062416" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:417
-xref: uniprot.ptm:PTM-0501
-is_a: MOD:00916
-is_a: MOD:01166
-
-[Term]
-id: MOD:02090
-name: O-(phospho-5'-uridine)-L-threonine
-def: "A protein modification that effectively modifies an L-threonine residue with 5'-phosphouridine through a phosphodiester bond to form O-(phospho-5'-uridine)-L-threonine." [DeltaMass:0, PubMed:22504181, Unimod:417#T, ChEBI:156052]
-subset: PSI-MOD-slim
-synonym: "MOD_RES O-UMP-threonine" EXACT UniProt-feature []
-synonym: "OUMPThr" EXACT PSI-MOD-label []
-synonym: "PhosphoUridine" RELATED PSI-MS-label []
-property_value: DiffAvg "306.17" xsd:float
-property_value: DiffFormula "C 9 H 11 N 2 O 8 P 1" xsd:string
-property_value: DiffMono "306.025302" xsd:float
-property_value: Formula "C 13 H 18 N 3 O 9 P 1" xsd:string
-property_value: MassAvg "391.27" xsd:float
-property_value: MassMono "391.078066" xsd:float
-property_value: Origin "T" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:417
-xref: uniprot.ptm:PTM-0502
-is_a: MOD:00917
-is_a: MOD:01166
-
-[Term]
-id: MOD:02091
-name: O-(phospho-5'-adenosine)-L-serine
-def: "A protein modification that effectively modifies an L-serine residue with 5'-phosphoadenosine through a phosphodiester bond to form O-(phospho-5'-adenosine)-L-serine." [PubMed:21472612, Unimod:405#S]
-subset: PSI-MOD-slim
-synonym: "MOD_RES O-AMP-serine" EXACT UniProt-feature []
-synonym: "Phosphoadenosine" RELATED PSI-MS-label []
-property_value: DiffAvg "329.21" xsd:float
-property_value: DiffFormula "C 10 H 12 N 5 O 6 P 1" xsd:string
-property_value: DiffMono "329.052520" xsd:float
-property_value: Formula "C 13 H 17 N 6 O 8 P 1" xsd:string
-property_value: MassAvg "416.28" xsd:float
-property_value: MassMono "416.084549" xsd:float
-property_value: Origin "S" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:405
-xref: uniprot.ptm:PTM-0651
-is_a: MOD:00916
-is_a: MOD:01165
-
-[Term]
-id: MOD:02092
-name: S-methylbutanedioic acid-L-cysteine
-def: "A protein modification that effectively converts an L-cysteine residue to form S-methylbutanedioic acid-L-cysteine by alkylation with itaconate through a thioether bond." [PubMed:29590092]
-subset: PSI-MOD-slim
-synonym: "MOD_RES S-(2,3-dicarboxypropyl)cysteine" EXACT UniProt-feature []
-property_value: DiffAvg "130.10" xsd:float
-property_value: DiffFormula "C 5 H 6 N 0 O 4 P 0 S 0" xsd:string
-property_value: DiffMono "130.026609" xsd:float
-property_value: Formula "C 8 H 11 N 1 O 5 P 0 S 1" xsd:string
-property_value: MassAvg "233.24" xsd:float
-property_value: MassMono "233.035793" xsd:float
-property_value: Origin "C" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0676
-is_a: MOD:00905
-is_a: MOD:00001
-
-[Term]
-id: MOD:02093
-name: N6-(2-hydroxyisobutanoyl)-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-(2-hydroxyisobutanoyl)-L-lysine." [PubMed:29775581, PubMed:24681537, ChEBI:144968, Unimod:1849]
-synonym: "MOD_RES N6-(2-hydroxyisobutyryl)lysine" EXACT UniProt-feature []
-property_value: DiffAvg "86.09" xsd:float
-property_value: DiffFormula "C 4 H 6 N 0 O 2" xsd:string
-property_value: DiffMono "86.036779" xsd:float
-property_value: Formula "C 10 H 18 N 2 O 3" xsd:string
-property_value: MassAvg "214.27" xsd:float
-property_value: MassMono "214.131742" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: Unimod:1849
-xref: uniprot.ptm:PTM-0638
-is_a: MOD:01875
-
-[Term]
-id: MOD:02094
-name: N6-((3R)-3-hydroxybutanoyl)-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-((3R)-3-hydroxybutanoyl)-L-lysine." [PubMed:27105115, ChEBI:149490]
-synonym: "MOD_RES N6-(beta-hydroxybutyryl)lysine" EXACT UniProt-feature []
-property_value: DiffAvg "86.09" xsd:float
-property_value: DiffFormula "C 4 H 6 N 0 O 2" xsd:string
-property_value: DiffMono "86.036779" xsd:float
-property_value: Formula "C 10 H 18 N 2 O 3" xsd:string
-property_value: MassAvg "214.27" xsd:float
-property_value: MassMono "214.131742" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0499
-is_a: MOD:01875
-
-[Term]
-id: MOD:02095
-name: N6-glutaryl-L-lysine
-def: "A protein modification that effectively converts an L-lysine residue to N6-glutaryl-L-lysine." [PubMed:24703693, ChEBI:87828]
-synonym: "MOD_RES N6-glutaryllysine" EXACT UniProt-feature []
-property_value: DiffAvg "114.10" xsd:float
-property_value: DiffFormula "C 5 H 6 N 0 O 3" xsd:string
-property_value: DiffMono "114.031694" xsd:float
-property_value: Formula "C 11 H 18 N 2 O 4" xsd:string
-property_value: MassAvg "242.28" xsd:float
-property_value: MassMono "242.126657" xsd:float
-property_value: Origin "K" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0487
-is_a: MOD:01875
-
-[Term]
-id: MOD:02096
-name: N4-methyl-D-asparagine
-def: "A protein modification that effectively converts a D-asparagine residue to N4-methyl-D-asparagine." [PubMed:22983711, ChEBI:149514]
-subset: PSI-MOD-slim
-synonym: "MOD_RES N4-methyl-D-asparagine" EXACT UniProt-feature []
-synonym: "N4-methylated D-asparagine" EXACT PSI-MOD-alternate []
-property_value: DiffAvg "14.03" xsd:float
-property_value: DiffFormula "C 1 H 2 N 0 O 0" xsd:string
-property_value: DiffMono "14.015650" xsd:float
-property_value: Formula "C 5 H 8 N 2 O 2" xsd:string
-property_value: MassAvg "128.13" xsd:float
-property_value: MassMono "128.058578" xsd:float
-property_value: Origin "N" xsd:string
-property_value: Source "natural" xsd:string
-xref: uniprot.ptm:PTM-0691
-is_a: MOD:00599
-is_a: MOD:00602
-is_a: MOD:00673
-is_a: MOD:02097
-is_a: MOD:00894
-
-[Term]
-id: MOD:02097
-name: modified D-asparagine residue
-def: "A protein modification that modifies a D-asparagine residue." [PubMed:18688235]
-subset: PSI-MOD-slim
-synonym: "ModDAsn" EXACT PSI-MOD-label []
-is_a: MOD:00203
-
-[Typedef]
-id: contains
-name: contains
-def: "'Entity A' contains 'Entity B' implies that 'Entity B' is a part of the structure of 'Entity A'." [PubMed:18688235]
-comment: The inverse relationship to \"part of\".
-is_transitive: true
-
-[Typedef]
-id: derives_from
-name: derives from
-def: "'Entity A' derives_from 'Entity B' implies that 'Entity A' is chemically derived from 'Entity B'." [PubMed:18688235]
-is_transitive: true
-
-[Typedef]
-id: has_functional_parent
-name: has functional parent
-def: "'Entity A' has_functional_parent 'Entity B' implies that 'Entity B' has at least one chacteristic group from which 'Entity A' can be derived by functional modification." [PubMed:18688235]
-comment: This relationship indicates that the formula and mass of the child are not inherited from the mass of the parent.
-is_transitive: true
-
-[Typedef]
-id: part_of
-name: part of
-def: "'Entity A' part_of 'Entity B' implies that 'Entity A' is a part of the structure of 'Entity B'." [PubMed:18688235]
-is_transitive: true
diff --git a/rustyms-generate-databases/data/RESID-RESIDUES.XML b/rustyms-generate-databases/data/RESID-RESIDUES.XML
deleted file mode 100644
index f21353e8..00000000
--- a/rustyms-generate-databases/data/RESID-RESIDUES.XML
+++ /dev/null
@@ -1,54807 +0,0 @@
-<?xml version="1.0" encoding="UTF-8" standalone="no"?>
-<!DOCTYPE Database SYSTEM "RESIDUES.DTD">
-<Database id="RESID" release="76.00" date="31-May-2018">
-<DBAuthor>John S. Garavelli</DBAuthor>
-<Address>Center for Bioinformatics &amp; Computational Biology, Delaware Biotechnology Institute, University of Delaware, 15 Innovation Way, Suite 205, Newark, DE  19711-5449, USA</Address>
-<Copyright>Copyright 2001, 2018 John S. Garavelli</Copyright>
-<DBdescription>The RESID Database is a comprehensive collection of annotations and structures for protein modifications including amino-terminal, carboxyl-terminal and peptide chain cross-link, pre-, co- and post-translational modifications.</DBdescription>
-<DBkeywords>amino acids, modified amino acids, protein modifications, protein structure</DBkeywords>
-<Entry id="AA0000">
-<Header>
-<Code>AA0000</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>20-Apr-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>alpha-amino acid</Name>
-<Xref>ChEBI:33710</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 2 H 3 N 1 O 1 +</Formula>
-<Weight type="chemical">57.05 +</Weight>
-<Weight type="physical">57.021464 +</Weight>
-</FormulaBlock>
-<ReferenceBlock>
-<Authors>
-<Anonymous />
-<Group>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN)</Group>
-</Authors>
-<Citation>Eur. J. Biochem. 138, 9-37, 1984</Citation>
-<Title>Nomenclature and symbolism for amino acids and peptides. Recommendations 1983.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1984.tb07877.x</Xref>
-<Xref>PMID:6692818</Xref>
-<Note>standard three-letter and one-letter symbols, and nomenclature</Note>
-</ReferenceBlock>
-<Comment>This entry represents an unknown or unidentified alpha-amino or alpha-imino carboxylic acid residue.</Comment>
-<SequenceCode>
-<SequenceSpec>X</SequenceSpec>
-<Abbreviation>Unk</Abbreviation>
-<Xref>PSI-MOD:00009</Xref>
-</SequenceCode>
-<Source>ambiguity</Source>
-<Image src="/images/AA0000.GIF" alt="DUMMY.GIF" />
-</Entry>
-<Entry id="AA0001">
-<Header>
-<Code>AA0001</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Sep-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-alanine</Name>
-<AlternateName>2-aminopropionic acid</AlternateName>
-<AlternateName>2-azanylpropanoic acid</AlternateName>
-<AlternateName>alpha-alanine</AlternateName>
-<AlternateName>alpha-aminopropionic acid</AlternateName>
-<SystematicName>(2S)-2-aminopropanoic acid</SystematicName>
-<Xref>CAS:56-41-7</Xref>
-<Xref>ChEBI:46217</Xref>
-<Xref>PDBHET:ALA</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 5 N 1 O 1</Formula>
-<Weight type="chemical">71.08</Weight>
-<Weight type="physical">71.037114</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0001" label="ALA">
-<Formula>C 0 H 0 N 0 O 0</Formula>
-<Weight type="chemical">0.00</Weight>
-<Weight type="physical">0.000000</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0004" label="ASP">
-<Formula>C -1 H 0 N 0 O -2</Formula>
-<Weight type="chemical">-44.01</Weight>
-<Weight type="physical">-43.989829</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Anonymous />
-<Group>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN)</Group>
-</Authors>
-<Citation>Eur. J. Biochem. 138, 9-37, 1984</Citation>
-<Title>Nomenclature and symbolism for amino acids and peptides. Recommendations 1983.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1984.tb07877.x</Xref>
-<Xref>PMID:6692818</Xref>
-<Note>standard three-letter and one-letter symbols, and nomenclature</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Jankowski, V.</Author>
-<Author>Vanholder, R.</Author>
-<Author>van der Giet, M.</Author>
-<Author>Tölle, M.</Author>
-<Author>Karadogan, S.</Author>
-<Author>Gobom, J.</Author>
-<Author>Furkert, J.</Author>
-<Author>Oksche, A.</Author>
-<Author>Krause, E.</Author>
-<Author>Tran, T.N.</Author>
-<Author>Tepel, M.</Author>
-<Author>Schuchardt, M.</Author>
-<Author>Schlüter, H.</Author>
-<Author>Wiedon, A.</Author>
-<Author>Beyermann, M.</Author>
-<Author>Bader, M.</Author>
-<Author>Todiras, M.</Author>
-<Author>Zidek, W.</Author>
-<Author>Jankowski, J.</Author>
-</Authors>
-<Citation>Arterioscler. Thromb. Vasc. Biol. 27, 297-302, 2007</Citation>
-<Title>Mass-spectrometric identification of a novel angiotensin peptide in human plasma.</Title>
-<Xref>DOI:10.1161/01.ATV.0000253889.09765.5f</Xref>
-<Xref>PMID:17138938</Xref>
-<Note>identification of an alanine residue apparently arising from a decarboxylated aspartic acid residue</Note>
-</ReferenceBlock>
-<Comment>Alanine has not been reported to act as an active site residue.</Comment>
-<SequenceCode link="ALA">
-<SequenceSpec>A</SequenceSpec>
-<Abbreviation>Ala</Abbreviation>
-<Xref>PSI-MOD:00010</Xref>
-</SequenceCode>
-<SequenceCode link="ASP">
-<SequenceSpec>D</SequenceSpec>
-<Xref>PSI-MOD:00869</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<FeatureNote>
-<Feature type="UniProt" link="ALA">Not available</Feature>
-<Note>UniProt has no active site feature annotations for this residue</Note>
-</FeatureNote>
-<Feature type="UniProt" key="mod_res__beta-decarboxylated aspartate__d" link="ASP">MOD_RES Beta-decarboxylated aspartate</Feature>
-</Features>
-<Image src="/images/AA0001.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0001.PDB" />
-</Entry>
-<Entry id="AA0002">
-<Header>
-<Code>AA0002</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Jun-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-arginine</Name>
-<AlternateName>2-amino-5-(carbamimidamido)pentanoic acid [tautomer]</AlternateName>
-<AlternateName>2-amino-5-guanidinopentanoic acid</AlternateName>
-<AlternateName>2-amino-5-guanidinovaleric acid</AlternateName>
-<AlternateName>2-amino-5-[(aminoiminomethyl)amino]pentanoic acid [tautomer]</AlternateName>
-<AlternateName>2-azanyl-5-[bis(azanyl)methylideneazanyl]pentanoic acid</AlternateName>
-<AlternateName>alpha-amino-delta-guanidinovaleric acid</AlternateName>
-<SystematicName>(2S)-2-amino-5-[(diaminomethylidene)amino]pentanoic acid</SystematicName>
-<Xref>CAS:74-79-3</Xref>
-<Xref>ChEBI:29952</Xref>
-<Xref>PDBHET:ARG</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 12 N 4 O 1</Formula>
-<Weight type="chemical">156.19</Weight>
-<Weight type="physical">156.101111</Weight>
-</FormulaBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Malinowski, D.P.</Author>
-<Author>Fridovich, I.</Author>
-</Authors>
-<Citation>Biochemistry 18, 5909-5917, 1979</Citation>
-<Title>Chemical modification of arginine at the active site of the bovine erythrocyte superoxide dismutase.</Title>
-<Xref>DOI:10.1021/bi00593a023</Xref>
-<Xref>PMID:518876</Xref>
-<Note>chemical modification of an active site arginine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Anonymous />
-<Group>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN)</Group>
-</Authors>
-<Citation>Eur. J. Biochem. 138, 9-37, 1984</Citation>
-<Title>Nomenclature and symbolism for amino acids and peptides. Recommendations 1983.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1984.tb07877.x</Xref>
-<Xref>PMID:6692818</Xref>
-<Note>standard three-letter and one-letter symbols, and nomenclature</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>R</SequenceSpec>
-<Abbreviation>Arg</Abbreviation>
-<Xref>PSI-MOD:00011</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="act_site____r">ACT_SITE</Feature>
-</Features>
-<Image src="/images/AA0002.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0002.PDB" />
-</Entry>
-<Entry id="AA0003">
-<Header>
-<Code>AA0003</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Sep-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-asparagine</Name>
-<AlternateName>2,4-bis(azanyl)-4-oxobutanoic acid</AlternateName>
-<AlternateName>2,4-diamino-4-oxobutanoic acid</AlternateName>
-<AlternateName>2-amino-3-carbamoylpropanoic acid</AlternateName>
-<AlternateName>2-amino-4-butanediamic acid</AlternateName>
-<AlternateName>2-aminosuccinamic acid</AlternateName>
-<AlternateName>2-aminosuccinic acid 4-amide</AlternateName>
-<AlternateName>alpha-amino-beta-carbamylpropionic acid</AlternateName>
-<AlternateName>alpha-aminosuccinamic acid</AlternateName>
-<AlternateName>aspartic acid 4-amide</AlternateName>
-<AlternateName>aspartic acid beta-amide</AlternateName>
-<AlternateName>beta-asparagine</AlternateName>
-<SystematicName>(2S)-2-amino-4-butanediamic acid</SystematicName>
-<Xref>CAS:70-47-3</Xref>
-<Xref>ChEBI:50347</Xref>
-<Xref>PDBHET:ASN</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 6 N 2 O 2</Formula>
-<Weight type="chemical">114.10</Weight>
-<Weight type="physical">114.042927</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0003" label="ASN">
-<Formula>C 0 H 0 N 0 O 0</Formula>
-<Weight type="chemical">0.00</Weight>
-<Weight type="physical">0.000000</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0004" label="ASP">
-<Formula>C 0 H 1 N 1 O -1</Formula>
-<Weight type="chemical">-0.98</Weight>
-<Weight type="physical">-0.984016</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Vauquelin, L.N.</Author>
-<Author>Robiquet, P.J.</Author>
-</Authors>
-<Citation>Ann. Chim. 57, 88-93, 1806</Citation>
-<Title>Découverte d'un nouveau principe végétal dans les Asperges (Asparagus sativus, Linn.)  [The discovery of a new plant principle in asparagus (Asparagus sativus, L.)].</Title>
-<Note>article in French; isolation and naming</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Drenth, J.</Author>
-<Author>Jansonius, J.N.</Author>
-<Author>Koekoek, R.</Author>
-<Author>Swen, H.M.</Author>
-<Author>Wolthers, B.G.</Author>
-</Authors>
-<Citation>Nature 218, 929-932, 1968</Citation>
-<Title>Structure of papain.</Title>
-<Xref>DOI:10.1038/218929a0</Xref>
-<Xref>PMID:5681232</Xref>
-<Note>asparagine as an active site residue in a thiol proteinase</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Anonymous />
-<Group>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN)</Group>
-</Authors>
-<Citation>Eur. J. Biochem. 138, 9-37, 1984</Citation>
-<Title>Nomenclature and symbolism for amino acids and peptides. Recommendations 1983.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1984.tb07877.x</Xref>
-<Xref>PMID:6692818</Xref>
-<Note>standard three-letter and one-letter symbols, and nomenclature</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Curnow, A.W.</Author>
-<Author>Tumbula, D.L.</Author>
-<Author>Pelaschier, J.T.</Author>
-<Author>Min, B.</Author>
-<Author>Soll, D.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 95, 12838-12843, 1998</Citation>
-<Title>Glutamyl-tRNA(Gln) amidotransferase in Deinococcus radiodurans may be confined to asparagine biosynthesis.</Title>
-<Xref>DOI:10.1073/pnas.95.22.12838</Xref>
-<Xref>PMID:9789001</Xref>
-<Note>"mischarged" aspartyl-tRNA(Asn) is amidated by glutamyl-tRNA(Gln) amidotransferase in Deinococcus radiodurans</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Paradisi, F.</Author>
-<Author>Dean, J.L.</Author>
-<Author>Geoghegan, K.F.</Author>
-<Author>Engel, P.C.</Author>
-</Authors>
-<Citation>Biochemistry 44, 3636-3643, 2005</Citation>
-<Title>Spontaneous chemical reversion of an active site mutation: deamidation of an asparagine residue replacing the catalytic aspartic acid of glutamate dehydrogenase.</Title>
-<Xref>DOI:10.1021/bi047679u</Xref>
-<Xref>PMID:15736973</Xref>
-<Note>an Asp to Asn mutation at an enzyme active site seemingly has partial activity; however, the asparagine form is shown to be inactive, and enhanced spontaneous deamidation results in the partial recovery of activity</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kolodkin-Gal, I.</Author>
-<Author>Hazan, R.</Author>
-<Author>Gaathon, A.</Author>
-<Author>Carmeli, S.</Author>
-<Author>Engelberg-Kulka, H.</Author>
-</Authors>
-<Citation>Science 318, 652-655, 2007</Citation>
-<Title>A linear pentapeptide is a quorum-sensing factor required for mazEF-mediated cell death in Escherichia coli.</Title>
-<Xref>DOI:10.1126/science.1147248</Xref>
-<Xref>PMID:17962566</Xref>
-<Note>enzymatic amidation of an aspartic acid residue in a peptide; the enzyme is currently identified by an activity that is different from the new activity</Note>
-</ReferenceBlock>
-<Comment>Some bacteria or archaea incorporate asparagine produced by the amidation of aspartyl-tRNA(Asn).</Comment>
-<GeneratingEnzyme>
-<EnzymeName link="ASN">aspartate--tRNA(Asn) ligase (EC 6.1.1.23)</EnzymeName>
-<EnzymeName link="ASN">asparaginyl-tRNA synthase (glutamine-hydrolysing) (EC 6.3.5.6)</EnzymeName>
-<EnzymeName link="ASP">aspartate--ammonia ligase (EC 6.3.1.1)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode link="ASN">
-<SequenceSpec>N</SequenceSpec>
-<Abbreviation>Asn</Abbreviation>
-<Xref>PSI-MOD:00012</Xref>
-</SequenceCode>
-<SequenceCode link="ASP">
-<SequenceSpec>D</SequenceSpec>
-<Xref>PSI-MOD:01185</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="act_site____n" link="ASN">ACT_SITE</Feature>
-<Feature type="UniProt" key="mod_res__amidated aspartic acid__d" link="ASP">MOD_RES Amidated aspartic acid</Feature>
-</Features>
-<Image src="/images/AA0003.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0003.PDB" />
-</Entry>
-<Entry id="AA0004">
-<Header>
-<Code>AA0004</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-Mar-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-aspartic acid</Name>
-<AlternateName>2-azanylbutanedioic acid</AlternateName>
-<AlternateName>aminosuccinic acid</AlternateName>
-<SystematicName>(2S)-2-aminobutanedioic acid</SystematicName>
-<Xref>CAS:56-84-8</Xref>
-<Xref>ChEBI:29958</Xref>
-<Xref>PDBHET:ASP</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 5 N 1 O 3</Formula>
-<Weight type="chemical">115.09</Weight>
-<Weight type="physical">115.026943</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0004" label="ASP">
-<Formula>C 0 H 0 N 0 O 0</Formula>
-<Weight type="chemical">0.00</Weight>
-<Weight type="physical">0.000000</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0003" label="ASN">
-<Formula>C 0 H -1 N -1 O 1</Formula>
-<Weight type="chemical">0.98</Weight>
-<Weight type="physical">0.984016</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Blow, D.M.</Author>
-<Author>Birktoft, J.J.</Author>
-<Author>Hartley, B.S.</Author>
-</Authors>
-<Citation>Nature 221, 337-340, 1969</Citation>
-<Title>Role of a buried acid group in the mechanism of action of chymotrypsin.</Title>
-<Xref>DOI:10.1038/221337a0</Xref>
-<Xref>PMID:5764436</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Birktoft, J.J.</Author>
-<Author>Blow, D.M.</Author>
-<Author>Henderson, R.</Author>
-<Author>Steitz, T.A.</Author>
-</Authors>
-<Citation>Philos. Trans. R. Soc. Lond., B, Biol. Sci. 257, 67-76, 1970</Citation>
-<Title>I. Serine proteinases. The structure of alpha-chymotrypsin.</Title>
-<Xref>PMID:4399050</Xref>
-<Note>X-ray diffraction</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sepulveda, P.</Author>
-<Author>Marciniszyn Jr., J.</Author>
-<Author>Liu, D.</Author>
-<Author>Tang, J.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 250, 5082-5088, 1975</Citation>
-<Title>Primary structure of porcine pepsin. III. Amino acid sequence of a cyanogen bromide fragment, CB2A, and the complete structure of porcine pepsin.</Title>
-<Xref>PMID:1097438</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Andreeva, N.S.</Author>
-<Author>Gustchina, A.E.</Author>
-<Author>Fedorov, A.A.</Author>
-<Author>Shutzkever, N.E.</Author>
-<Author>Volnova, T.V.</Author>
-</Authors>
-<Citation>Adv. Exp. Med. Biol. 95, 23-31, 1977</Citation>
-<Title>X-ray crystallographic studies of pepsin.</Title>
-<Xref>PMID:339692</Xref>
-<Note>X-ray diffraction, 2.7-3.0 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Anonymous />
-<Group>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN)</Group>
-</Authors>
-<Citation>Eur. J. Biochem. 138, 9-37, 1984</Citation>
-<Title>Nomenclature and symbolism for amino acids and peptides. Recommendations 1983.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1984.tb07877.x</Xref>
-<Xref>PMID:6692818</Xref>
-<Note>standard three-letter and one-letter symbols, and nomenclature</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Stewart, A.E.</Author>
-<Author>Arfin, S.M.</Author>
-<Author>Bradshaw, R.A.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 269, 23509-23517, 1994</Citation>
-<Title>Protein NH2-terminal asparagine deamidase. Isolation and characterization of a new enzyme.</Title>
-<Xref>PMID:8089117</Xref>
-<Note>enzyme that deamidates amino-terminal asparagine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Jedrzejewski, P.T.</Author>
-<Author>Girod, A.</Author>
-<Author>Tholey, A.</Author>
-<Author>Koenig, N.</Author>
-<Author>Thullner, S.</Author>
-<Author>Kinzel, V.</Author>
-<Author>Bossemeyer, D.</Author>
-</Authors>
-<Citation>Protein Sci. 7, 457-469, 1998</Citation>
-<Title>A conserved deamidation site at Asn 2 in the catalytic subunit of mammalian cAMP-dependent protein kinase detected by capillary LC-MS and tandem mass spectrometry.</Title>
-<Xref>DOI:10.1002/pro.5560070227</Xref>
-<Xref>PMID:9521123</Xref>
-<Note>chromatographic and mass spectrometric identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lindner, H.</Author>
-<Author>Sarg, B.</Author>
-<Author>Hoertnagl, B.</Author>
-<Author>Helliger, W.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 273, 13324-13330, 1998</Citation>
-<Title>The microheterogeneity of the mammalian H1(0) histone. Evidence for an age-dependent deamidation.</Title>
-<Xref>DOI:10.1074/jbc.273.21.13324</Xref>
-<Xref>PMID:9582379</Xref>
-<Note>this deamidation may be non-enzymatic</Note>
-</ReferenceBlock>
-<Comment>Some active site aspartic acids may form transient covalent bonds with substrates that are not distinguished in protein sequence database features.</Comment>
-<Comment>The deamidation of asparagine is coupled with myristoylation of the immediately preceding glycine (see RESID:AA0059).</Comment>
-<GeneratingEnzyme>
-<EnzymeName link="ASN">protein NH2-terminal asparagine deamidase (EC 3.5.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode link="ASP">
-<SequenceSpec>D</SequenceSpec>
-<Abbreviation>Asp</Abbreviation>
-<Xref>PSI-MOD:00013</Xref>
-</SequenceCode>
-<SequenceCode link="ASN">
-<SequenceSpec>N</SequenceSpec>
-<Condition>incidental to RESID:AA0059</Condition>
-<Xref>PSI-MOD:00684</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="act_site____d" link="ASP">ACT_SITE</Feature>
-<Feature type="UniProt" key="mod_res__deamidated asparagine__n" link="ASN">MOD_RES Deamidated asparagine</Feature>
-</Features>
-<Image src="/images/AA0004.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0004.PDB" />
-</Entry>
-<Entry id="AA0005">
-<Header>
-<Code>AA0005</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-cysteine</Name>
-<AlternateName>(R)-cysteine</AlternateName>
-<AlternateName>2-amino-3-mercaptopropanoic acid</AlternateName>
-<AlternateName>2-amino-3-mercaptopropionic acid</AlternateName>
-<AlternateName>2-azanyl-3-sulfanylpropanoic acid</AlternateName>
-<AlternateName>3-mercapto-L-alanine</AlternateName>
-<AlternateName>alpha-amino-beta-mercaptopropanoic acid</AlternateName>
-<AlternateName>alpha-amino-beta-mercaptopropionic acid</AlternateName>
-<AlternateName>alpha-amino-beta-thiolpropionic acid</AlternateName>
-<AlternateName>beta-mercaptoalanine</AlternateName>
-<AlternateName>half-cystine</AlternateName>
-<AlternateName>L-(+)-cysteine</AlternateName>
-<AlternateName>thioserine</AlternateName>
-<SystematicName>(2R)-2-amino-3-sulfanylpropanoic acid</SystematicName>
-<Xref>CAS:4371-52-2</Xref>
-<Xref>CAS:52-90-4</Xref>
-<Xref>ChEBI:29950</Xref>
-<Xref>PDBHET:CYS</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 5 N 1 O 1 S 1</Formula>
-<Weight type="chemical">103.14</Weight>
-<Weight type="physical">103.009185</Weight>
-</FormulaBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Grau, U.M.</Author>
-<Author>Trommer, W.E.</Author>
-<Author>Rossmann, M.G.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 151, 289-307, 1981</Citation>
-<Title>Structure of the active ternary complex of pig heart lactate dehydrogenase with S-lac-NAD at 2.7 angstrom resolution.</Title>
-<Xref>DOI:10.1016/0022-2836(81)90516-7</Xref>
-<Xref>PMID:7338899</Xref>
-<Note>X-ray diffraction, 2.7 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Anonymous />
-<Group>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN)</Group>
-</Authors>
-<Citation>Eur. J. Biochem. 138, 9-37, 1984</Citation>
-<Title>Nomenclature and symbolism for amino acids and peptides. Recommendations 1983.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1984.tb07877.x</Xref>
-<Xref>PMID:6692818</Xref>
-<Note>standard three-letter and one-letter symbols, and nomenclature</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Takishima, K.</Author>
-<Author>Mamiya, G.</Author>
-</Authors>
-<Citation>Protein Seq. Data Anal. 1, 103-106, 1987</Citation>
-<Title>Location of the essential cysteine residue of jack bean urease.</Title>
-<Xref>PMID:3447159</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wagner, A.F.V.</Author>
-<Author>Frey, M.</Author>
-<Author>Neugebauer, F.A.</Author>
-<Author>Schäfer, D.</Author>
-<Author>Knappe, J.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 89, 996-1000, 1992</Citation>
-<Title>The free radical in pyruvate formate-lyase is located on glycine-734.</Title>
-<Xref>DOI:10.1073/pnas.89.3.996</Xref>
-<Xref>PMID:1310545</Xref>
-<Note>evidence for intermediate cysteine thiyl radical</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sauerwald, A.</Author>
-<Author>Zhu, W.</Author>
-<Author>Major, T.A.</Author>
-<Author>Roy, H.</Author>
-<Author>Palioura, S.</Author>
-<Author>Jahn, D.</Author>
-<Author>Whitman, W.B.</Author>
-<Author>Yates 3rd, J.R.</Author>
-<Author>Ibba, M.</Author>
-<Author>Söll, D.</Author>
-</Authors>
-<Citation>Science 307, 1969-1972, 2005</Citation>
-<Title>RNA-dependent cysteine biosynthesis in archaea.</Title>
-<Xref>DOI:10.1126/science.1108329</Xref>
-<Xref>PMID:15790858</Xref>
-</ReferenceBlock>
-<Comment>Some methanogenic archaea incorporate cysteine produced by the transsulfuration of O-phosphoserine-tRNA(Cys).</Comment>
-<Comment>Some active site cysteines may form transient covalent bonds with substrates that are not distinguished in protein sequence database features.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>O-phosphoserine--tRNA(Cys) ligase</EnzymeName>
-<EnzymeName>O-phospho-L-seryl-tRNA:Cys-tRNA synthase (EC 2.5.1.73)</EnzymeName>
-<EnzymeName>O-phospho-L-serine:tRNA(Cys) ligase (AMP-forming) (EC 6.1.1.27)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Abbreviation>Cys</Abbreviation>
-<Xref>PSI-MOD:00014</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="act_site____c">ACT_SITE</Feature>
-<Feature type="UniProt" key="act_site__cysteine radical intermediate__c">ACT_SITE Cysteine radical intermediate</Feature>
-</Features>
-<Image src="/images/AA0005.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0005.PDB" />
-</Entry>
-<Entry id="AA0006">
-<Header>
-<Code>AA0006</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>13-Sep-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-glutamic acid</Name>
-<AlternateName>1-aminopropane-1,3-dicarboxylic acid</AlternateName>
-<AlternateName>2-aminoglutaric acid</AlternateName>
-<AlternateName>2-azanylpentanedioic acid</AlternateName>
-<AlternateName>alpha-aminoglutaric acid</AlternateName>
-<AlternateName>glutaminic acid</AlternateName>
-<SystematicName>(2S)-2-aminopentanedioic acid</SystematicName>
-<Xref>CAS:56-86-0</Xref>
-<Xref>ChEBI:29972</Xref>
-<Xref>PDBHET:GLU</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 7 N 1 O 3</Formula>
-<Weight type="chemical">129.12</Weight>
-<Weight type="physical">129.042593</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0006" label="GLU">
-<Formula>C 0 H 0 N 0 O 0</Formula>
-<Weight type="chemical">0.00</Weight>
-<Weight type="physical">0.000000</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0007" label="GLN">
-<Formula>C 0 H -1 N -1 O 1</Formula>
-<Weight type="chemical">0.98</Weight>
-<Weight type="physical">0.984016</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
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-</Authors>
-<Citation>Biochemistry 10, 146-154, 1971</Citation>
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-</ReferenceBlock>
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-</Authors>
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-<Title>Identification of a glutamic acid at the active center of bovine carboxypeptidase B.</Title>
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-</Authors>
-<Citation>J. Mol. Biol. 103, 175-190, 1976</Citation>
-<Title>Structure of carboxypeptidase B at 2.8 angstrom resolution.</Title>
-<Xref>DOI:10.1016/0022-2836(76)90058-9</Xref>
-<Xref>PMID:957425</Xref>
-<Note>X-ray diffraction, 2.8 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Anonymous />
-<Group>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN)</Group>
-</Authors>
-<Citation>Eur. J. Biochem. 138, 9-37, 1984</Citation>
-<Title>Nomenclature and symbolism for amino acids and peptides. Recommendations 1983.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1984.tb07877.x</Xref>
-<Xref>PMID:6692818</Xref>
-<Note>standard three-letter and one-letter symbols, and nomenclature</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
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-<Author>Collins, E.J.</Author>
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-</Authors>
-<Citation>Proteins 10, 251-259, 1991</Citation>
-<Title>Structure of ricin A-chain at 2.5 angstroms.</Title>
-<Xref>DOI:10.1002/prot.340100309</Xref>
-<Xref>PMID:1881881</Xref>
-<Note>X-ray diffraction, 2.5 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Schmidt, G.</Author>
-<Author>Sehr, P.</Author>
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-</Authors>
-<Citation>Nature 387, 725-729, 1997</Citation>
-<Title>Gln 63 of Rho is deamidated by Escherichia coli cytotoxic necrotizing factor-1.</Title>
-<Xref>DOI:10.1038/42735</Xref>
-<Xref>PMID:9192900</Xref>
-<Note>enzymatic deamidation of glutamine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Striebel, F.</Author>
-<Author>Imkamp, F.</Author>
-<Author>Sutter, M.</Author>
-<Author>Steiner, M.</Author>
-<Author>Mamedov, A.</Author>
-<Author>Weber-Ban, E.</Author>
-</Authors>
-<Citation>Nature Struct. Mol. Biol. 16, 647-651, 2009</Citation>
-<Title>Bacterial ubiquitin-like modifier Pup is deamidated and conjugated to substrates by distinct but homologous enzymes.</Title>
-<Xref>DOI:10.1038/nsmb.1597</Xref>
-<Xref>PMID:19448618</Xref>
-<Note>Pup activated through deamidation of C-terminal glutamine by depupylase/deamidase Dop</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Horiguchi, Y.</Author>
-<Author>Inoue, N.</Author>
-<Author>Masuda, M.</Author>
-<Author>Kashimoto, T.</Author>
-<Author>Katahira, J.</Author>
-<Author>Sugimoto, N.</Author>
-<Author>Matsuda, M.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 94, 11623-11626, 1997</Citation>
-<Title>Bordetella bronchiseptica dermonecrotizing toxin induces reorganization of actin stress fibers through deamidation of Gln-63 of the GTP-binding protein Rho.</Title>
-<Xref>DOI:10.1073/pnas.94.21.11623</Xref>
-<Xref>PMID:9326660</Xref>
-<Note>enzymatic deamidation of glutamine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wang, H.</Author>
-<Author>Piatkov, K.I.</Author>
-<Author>Brower, C.S.</Author>
-<Author>Varshavsky, A.</Author>
-</Authors>
-<Citation>Mol. Cell 34, 686-695, 2009</Citation>
-<Title>Glutamine-specific N-terminal amidase, a component of the N-end rule pathway.</Title>
-<Xref>DOI:10.1016/j.molcel.2009.04.032</Xref>
-<Xref>PMID:19560421</Xref>
-<Note>enzymatic deamidation of N-terminal glutamine targets a protein for degradation</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Cui, J.</Author>
-<Author>Yao, Q.</Author>
-<Author>Li, S.</Author>
-<Author>Ding, X.</Author>
-<Author>Lu, Q.</Author>
-<Author>Mao, H.</Author>
-<Author>Liu, L.</Author>
-<Author>Zheng, N.</Author>
-<Author>Chen, S.</Author>
-<Author>Shao, F.</Author>
-</Authors>
-<Citation>Science 329, 1215-1218, 2010</Citation>
-<Title>Glutamine deamidation and dysfunction of ubiquitin/NEDD8 induced by a bacterial effector family.</Title>
-<Xref>DOI:10.1126/science.1193844</Xref>
-<Xref>PMID:20688984</Xref>
-<Note>deamidation of glutamine in host ubiquitin is catalyzed by Cif homolog of enteropathogenic bacteria</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Cruz-Migoni, A.</Author>
-<Author>Hautbergue, G.M.</Author>
-<Author>Artymiuk, P.J.</Author>
-<Author>Baker, P.J.</Author>
-<Author>Bokori-Brown, M.</Author>
-<Author>Chang, C.T.</Author>
-<Author>Dickman, M.J.</Author>
-<Author>Essex-Lopresti, A.</Author>
-<Author>Harding, S.V.</Author>
-<Author>Mahadi, N.M.</Author>
-<Author>Marshall, L.E.</Author>
-<Author>Mobbs, G.W.</Author>
-<Author>Mohamed, R.</Author>
-<Author>Nathan, S.</Author>
-<Author>Ngugi, S.A.</Author>
-<Author>Ong, C.</Author>
-<Author>Ooi, W.F.</Author>
-<Author>Partridge, L.J.</Author>
-<Author>Phillips, H.L.</Author>
-<Author>Raih, M.F.</Author>
-<Author>Ruzheinikov, S.</Author>
-<Author>Sarkar-Tyson, M.</Author>
-<Author>Sedelnikova, S.E.</Author>
-<Author>Smither, S.J.</Author>
-<Author>Tan, P.</Author>
-<Author>Titball, R.W.</Author>
-<Author>Wilson, S.A.</Author>
-<Author>Rice, D.W.</Author>
-</Authors>
-<Citation>Science 334, 821-824, 2011</Citation>
-<Title>A Burkholderia pseudomallei toxin inhibits helicase activity of translation factor eIF4A.</Title>
-<Xref>DOI:10.1126/science.1211915</Xref>
-<Xref>PMID:22076380</Xref>
-<Note>deamidation of glutamine in host eIF4A is catalyzed by lethal factor 1 of enteropathogenic bacteria</Note>
-</ReferenceBlock>
-<Comment>Some active site glutamic acids may form transient covalent bonds with substrates that are not distinguished in protein sequence database features.</Comment>
-<GeneratingEnzyme>
-<EnzymeName> protein-glutamine glutaminase (EC 3.5.1.44)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode link="GLU">
-<SequenceSpec>E</SequenceSpec>
-<Abbreviation>Glu</Abbreviation>
-<Xref>PSI-MOD:00015</Xref>
-</SequenceCode>
-<SequenceCode link="GLN">
-<SequenceSpec>Q</SequenceSpec>
-<Xref>PSI-MOD:00685</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="act_site____e" link="GLU">ACT_SITE</Feature>
-<Feature type="UniProt" key="mod_res__deamidated glutamine__q" link="GLN">MOD_RES Deamidated glutamine</Feature>
-</Features>
-<Image src="/images/AA0006.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0006.PDB" />
-</Entry>
-<Entry id="AA0007">
-<Header>
-<Code>AA0007</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Jun-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-glutamine</Name>
-<AlternateName>2,5-bis(azanyl)-5-oxopentanoic acid</AlternateName>
-<AlternateName>2,5-diamino-5-oxopentanoic acid</AlternateName>
-<AlternateName>2-amino-4-carbamoylbutanoic acid</AlternateName>
-<AlternateName>2-aminoglutaramic acid</AlternateName>
-<AlternateName>alpha-amino-gamma-carbamylbutyric acid</AlternateName>
-<AlternateName>glutamic acid 5-amide</AlternateName>
-<AlternateName>glutamic acid gamma-amide</AlternateName>
-<AlternateName>glutamide</AlternateName>
-<SystematicName>(2S)-2-amino-5-pentanediamic acid</SystematicName>
-<Xref>CAS:56-85-9</Xref>
-<Xref>ChEBI:30011</Xref>
-<Xref>PDBHET:GLN</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 8 N 2 O 2</Formula>
-<Weight type="chemical">128.13</Weight>
-<Weight type="physical">128.058578</Weight>
-</FormulaBlock>
-<ReferenceBlock>
-<Authors>
-<Anonymous />
-<Group>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN)</Group>
-</Authors>
-<Citation>Eur. J. Biochem. 138, 9-37, 1984</Citation>
-<Title>Nomenclature and symbolism for amino acids and peptides. Recommendations 1983.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1984.tb07877.x</Xref>
-<Xref>PMID:6692818</Xref>
-<Note>standard three-letter and one-letter symbols, and nomenclature</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Schon, A.</Author>
-<Author>Kannangara, C.G.</Author>
-<Author>Gough, S.</Author>
-<Author>Soll, D.</Author>
-</Authors>
-<Citation>Nature 331, 187-190, 1988</Citation>
-<Title>Protein biosynthesis in organelles requires misaminoacylation of tRNA.</Title>
-<Xref>DOI:10.1038/331187a0</Xref>
-<Xref>PMID:3340166</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Curnow, A.W.</Author>
-<Author>Hong, K.W.</Author>
-<Author>Yuan, R.</Author>
-<Author>Kim, S.I.</Author>
-<Author>Martins, O.</Author>
-<Author>Winkler, W.</Author>
-<Author>Henkin, T.M.</Author>
-<Author>Soll, D.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 94, 11819-11826, 1997</Citation>
-<Title>Glu-tRNA(Gln) amidotransferase: a novel heterotrimeric enzyme required for correct decoding of glutamine codons during translation.</Title>
-<Xref>DOI:10.1073/pnas.94.22.11819</Xref>
-<Xref>PMID:9342321</Xref>
-</ReferenceBlock>
-<Comment>Glutamine has not been reported to act as active site residue.</Comment>
-<Comment>Eukaryotic organelles, along with some bacteria and archaea incorporate glutamine produced by the amidation of "missacylated" glutamyl-tRNA(Gln).</Comment>
-<GeneratingEnzyme>
-<EnzymeName>glutaminyl-tRNA synthase (glutamine-hydrolysing) (EC 6.3.5.7)</EnzymeName>
-<EnzymeName>glutamate--tRNA(Gln) ligase (EC 6.1.1.24)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>Q</SequenceSpec>
-<Abbreviation>Gln</Abbreviation>
-<Xref>PSI-MOD:00016</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>UniProt has no active site feature annotations for this residue</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0007.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0007.PDB" />
-</Entry>
-<Entry id="AA0008">
-<Header>
-<Code>AA0008</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Jun-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>glycine</Name>
-<AlternateName>aminoacetic acid</AlternateName>
-<AlternateName>azanylethanoic acid</AlternateName>
-<AlternateName>glycocoll</AlternateName>
-<SystematicName>aminoethanoic acid</SystematicName>
-<Xref>CAS:56-40-6</Xref>
-<Xref>ChEBI:29947</Xref>
-<Xref>PDBHET:GLY</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 2 H 3 N 1 O 1</Formula>
-<Weight type="chemical">57.05</Weight>
-<Weight type="physical">57.021464</Weight>
-</FormulaBlock>
-<ReferenceBlock>
-<Authors>
-<Anonymous />
-<Group>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN)</Group>
-</Authors>
-<Citation>Eur. J. Biochem. 138, 9-37, 1984</Citation>
-<Title>Nomenclature and symbolism for amino acids and peptides. Recommendations 1983.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1984.tb07877.x</Xref>
-<Xref>PMID:6692818</Xref>
-<Note>standard three-letter and one-letter symbols, and nomenclature</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wagner, A.F.V.</Author>
-<Author>Frey, M.</Author>
-<Author>Neugebauer, F.A.</Author>
-<Author>Schäfer, D.</Author>
-<Author>Knappe, J.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 89, 996-1000, 1992</Citation>
-<Title>The free radical in pyruvate formate-lyase is located on glycine-734.</Title>
-<Xref>DOI:10.1073/pnas.89.3.996</Xref>
-<Xref>PMID:1310545</Xref>
-<Note>evidence for stabilized glycine radical</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>G</SequenceSpec>
-<Abbreviation>Gly</Abbreviation>
-<Xref>PSI-MOD:00017</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="mod_res__glycine radical__g">MOD_RES Glycine radical</Feature>
-</Features>
-<Image src="/images/AA0008.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0008.PDB" />
-</Entry>
-<Entry id="AA0009">
-<Header>
-<Code>AA0009</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>04-May-2001</StrucRevDate>
-<TextChngDate>30-Jun-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-histidine</Name>
-<AlternateName>(2S)-2-amino-3-(1H-imidazol-5-yl)propanoic acid [tautomer]</AlternateName>
-<AlternateName>2-azanyl-3-(1H-imidazol-4-yl)propanoic acid</AlternateName>
-<AlternateName>2-azanyl-3-(1H-imidazol-5-yl)propanoic acid [tautomer]</AlternateName>
-<AlternateName>4-(2-amino-2-carboxyethyl)imidazole</AlternateName>
-<AlternateName>alpha-amino-beta-(4-imidazole)propionic acid</AlternateName>
-<AlternateName>glyoxaline-5-alanine</AlternateName>
-<SystematicName>(2S)-2-amino-3-(1H-imidazol-4-yl)propanoic acid</SystematicName>
-<Xref>CAS:71-00-1</Xref>
-<Xref>ChEBI:29979</Xref>
-<Xref>PDBHET:HIS</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 7 N 3 O 1</Formula>
-<Weight type="chemical">137.14</Weight>
-<Weight type="physical">137.058912</Weight>
-</FormulaBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kossel, A.</Author>
-</Authors>
-<Citation>Hoppe-Seyler's Z. Physiol. Chem. 22, 176-187, 1896</Citation>
-<Title>Ueber die basischen Stoffe des Zellkerns [On the basic substances of the nucleus].</Title>
-<Xref>DOI:10.1515/bchm2.1897.22.2.176</Xref>
-<Xref>http://vlp.mpiwg-berlin.mpg.de/library/data/lit17105?</Xref>
-<Note>article in German; isolation, crystallization and naming</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hedin, S.G.</Author>
-</Authors>
-<Citation>Hoppe-Seyler's Z. Physiol. Chem. 22, 191-195, 1896</Citation>
-<Title>Zur Kenntniss der Spaltungsproducte der Proteïinkörper [Toward knowledge of the cleavage products of proteins].</Title>
-<Xref>DOI:10.1515/bchm2.1897.22.2.191</Xref>
-<Xref>http://vlp.mpiwg-berlin.mpg.de/library/data/lit17107?</Xref>
-<Note>article in German; determination of molecular weight and elemental composition</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Pauly, H.</Author>
-</Authors>
-<Citation>Hoppe-Seyler's Z. Physiol. Chem. 42, 508-518, 1904</Citation>
-<Title>Über die Konstitution des Histidins. I. Mitteilung  [On the constitution of histidine. I. Communication].</Title>
-<Xref>DOI:10.1515/bchm2.1904.42.5-6.508</Xref>
-<Xref>http://vlp.mpiwg-berlin.mpg.de/library/data/lit18003?</Xref>
-<Note>article in German; determination of molecular structure</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Pyman, F.L.</Author>
-</Authors>
-<Citation>J. Chem. Soc. Trans. 99, 1386-1401, 1911</Citation>
-<Title>CLVII. - The synthesis of histidine.</Title>
-<Xref>DOI:10.1039/CT9119901386</Xref>
-<Note>chemical synthesis; proof of structure and relative stereochemistry</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Heinrikson, R.L.</Author>
-<Author>Stein, W.H.</Author>
-<Author>Crestfield, A.M.</Author>
-<Author>Moore, S.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 240, 2921-2934, 1965</Citation>
-<Title>The reactivities of the histidine residues at the active site of ribonuclease toward halo acids of different structures.</Title>
-<Xref>PMID:14342316</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wyckoff, H.W.</Author>
-<Author>Tsernoglou, D.</Author>
-<Author>Hanson, A.W.</Author>
-<Author>Knox, J.R.</Author>
-<Author>Lee, B.</Author>
-<Author>Richards, F.M.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 245, 305-328, 1970</Citation>
-<Title>The three-dimensional structure of ribonuclease-S. Interpretation of an electron density map at a nominal resolution of 2 A.</Title>
-<Xref>PMID:5460889</Xref>
-<Note>X-ray diffraction, 2.0 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bode, W.</Author>
-<Author>Schwager, P.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 98, 693-717, 1975</Citation>
-<Title>The refined crystal structure of bovine beta-trypsin at 1.8 angstrom resolution.</Title>
-<Xref>DOI:10.1016/S0022-2836(75)80005-2</Xref>
-<Xref>PMID:512</Xref>
-<Note>X-ray diffraction, 1.8 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Swenson, R.P.</Author>
-<Author>Williams Jr., C.H.</Author>
-<Author>Massey, V.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 258, 497-502, 1983</Citation>
-<Title>Identification of the histidine residue in D-amino acid oxidase that is covalently modified during inactivation by 5-dimethylaminonaphthalene-1-sulfonyl chloride.</Title>
-<Xref>PMID:6129252</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Dijkstra, B.W.</Author>
-<Author>Renetseder, R.</Author>
-<Author>Kalk, K.H.</Author>
-<Author>Hol, W.G.J.</Author>
-<Author>Drenth, J.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 168, 163-179, 1983</Citation>
-<Title>Structure of porcine pancreatic phospholipase A-2 at 2.6 angstrom resolution and comparison with bovine phospholipase A-2.</Title>
-<Xref>DOI:10.1016/S0022-2836(83)80328-3</Xref>
-<Xref>PMID:6876174</Xref>
-<Note>X-ray diffraction, 2.6 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Anonymous />
-<Group>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN)</Group>
-</Authors>
-<Citation>Eur. J. Biochem. 138, 9-37, 1984</Citation>
-<Title>Nomenclature and symbolism for amino acids and peptides. Recommendations 1983.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1984.tb07877.x</Xref>
-<Xref>PMID:6692818</Xref>
-<Note>standard three-letter and one-letter symbols, and nomenclature</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>van den Bergh, C.J.</Author>
-<Author>Slotboom, A.J.</Author>
-<Author>Verheij, H.M.</Author>
-<Author>de Haas, G.H.</Author>
-</Authors>
-<Citation>J. Cell. Biochem. 39, 379-390, 1989</Citation>
-<Title>The role of Asp-49 and other conserved amino acids in phospholipases A2 and their importance for enzymatic activity.</Title>
-<Xref>DOI:10.1002/jcb.240390404</Xref>
-<Xref>PMID:2722967</Xref>
-</ReferenceBlock>
-<Comment>Some active site histidines may form transient covalent bonds with substrates that are not distinguished in protein sequence database features.</Comment>
-<SequenceCode>
-<SequenceSpec>H</SequenceSpec>
-<Abbreviation>His</Abbreviation>
-<Xref>PSI-MOD:00018</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="act_site____h">ACT_SITE</Feature>
-</Features>
-<Image src="/images/AA0009.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0009.PDB" />
-</Entry>
-<Entry id="AA0010">
-<Header>
-<Code>AA0010</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Jun-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-isoleucine</Name>
-<AlternateName>2-azanyl-3-methylpentanoic acid</AlternateName>
-<AlternateName>3-methyl-norvaline</AlternateName>
-<AlternateName>alpha-amino-beta-methylvaleric acid</AlternateName>
-<AlternateName>L-erythro-isoleucine</AlternateName>
-<SystematicName>(2S,3S)-2-amino-3-methylpentanoic acid</SystematicName>
-<Xref>CAS:73-32-5</Xref>
-<Xref>ChEBI:30009</Xref>
-<Xref>PDBHET:ILE</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 11 N 1 O 1</Formula>
-<Weight type="chemical">113.16</Weight>
-<Weight type="physical">113.084064</Weight>
-</FormulaBlock>
-<ReferenceBlock>
-<Authors>
-<Anonymous />
-<Group>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN)</Group>
-</Authors>
-<Citation>Eur. J. Biochem. 138, 9-37, 1984</Citation>
-<Title>Nomenclature and symbolism for amino acids and peptides. Recommendations 1983.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1984.tb07877.x</Xref>
-<Xref>PMID:6692818</Xref>
-<Note>standard three-letter and one-letter symbols, and nomenclature</Note>
-</ReferenceBlock>
-<Comment>The alpha carboxyl group of a C-terminal isoleucine is predicted to act as a proton acceptor in the active site of an enzyme.</Comment>
-<SequenceCode>
-<SequenceSpec>I</SequenceSpec>
-<Abbreviation>Ile</Abbreviation>
-<Xref>PSI-MOD:00019</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="act_site__proton acceptor; via carboxylate__i">ACT_SITE Proton acceptor; via carboxylate</Feature>
-</Features>
-<Image src="/images/AA0010.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0010.PDB" />
-</Entry>
-<Entry id="AA0011">
-<Header>
-<Code>AA0011</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Jun-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-leucine</Name>
-<AlternateName>2-azanyl-4-methylpentanoic acid</AlternateName>
-<AlternateName>4-methyl-norvaline</AlternateName>
-<AlternateName>alpha-amino-gamma-methylvaleric acid</AlternateName>
-<AlternateName>alpha-aminoisocaproic acid</AlternateName>
-<SystematicName>(2S)-2-amino-4-methylpentanoic acid</SystematicName>
-<Xref>CAS:61-90-5</Xref>
-<Xref>ChEBI:30006</Xref>
-<Xref>PDBHET:LEU</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 11 N 1 O 1</Formula>
-<Weight type="chemical">113.16</Weight>
-<Weight type="physical">113.084064</Weight>
-</FormulaBlock>
-<ReferenceBlock>
-<Authors>
-<Anonymous />
-<Group>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN)</Group>
-</Authors>
-<Citation>Eur. J. Biochem. 138, 9-37, 1984</Citation>
-<Title>Nomenclature and symbolism for amino acids and peptides. Recommendations 1983.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1984.tb07877.x</Xref>
-<Xref>PMID:6692818</Xref>
-<Note>standard three-letter and one-letter symbols, and nomenclature</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Farazi, T.A.</Author>
-<Author>Manchester, J.K.</Author>
-<Author>Waksman, G.</Author>
-<Author>Gordon, J.I.</Author>
-</Authors>
-<Citation>Biochemistry 40, 9177-9186, 2001</Citation>
-<Title>Pre-steady-state kinetic studies of Saccharomyces cerevisiae myristoylCoA:protein N-myristoyltransferase mutants identify residues involved in catalysis.</Title>
-<Xref>DOI:10.1021/bi0107997</Xref>
-<Xref>PMID:11478885</Xref>
-<Note>the alpha carboxyl group of a C-terminal leucine is reported to act as a proton acceptor in the active site of an enzyme</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>L</SequenceSpec>
-<Abbreviation>Leu</Abbreviation>
-<Xref>PSI-MOD:00020</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="act_site__proton acceptor; via carboxylate__l">ACT_SITE Proton acceptor; via carboxylate</Feature>
-</Features>
-<Image src="/images/AA0011.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0011.PDB" />
-</Entry>
-<Entry id="AA0012">
-<Header>
-<Code>AA0012</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Jun-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-lysine</Name>
-<AlternateName>2,6-bis(azanyl)hexanoic acid</AlternateName>
-<AlternateName>6-amino-L-norleucine</AlternateName>
-<AlternateName>alpha,epsilon-diaminocaproic acid</AlternateName>
-<SystematicName>(2S)-2,6-diaminohexanoic acid</SystematicName>
-<Xref>CAS:56-87-1</Xref>
-<Xref>ChEBI:29967</Xref>
-<Xref>PDBHET:LYS</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 12 N 2 O 1</Formula>
-<Weight type="chemical">128.18</Weight>
-<Weight type="physical">128.094963</Weight>
-</FormulaBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Swenson, R.P.</Author>
-<Author>Williams Jr., C.H.</Author>
-<Author>Massey, V.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 257, 1937-1944, 1982</Citation>
-<Title>Chemical modification of D-amino acid oxidase. Amino acid sequence of the tryptic peptides containing tyrosine and lysine residues modified by fluorodinitrobenzene.</Title>
-<Xref>PMID:6120171</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Anonymous />
-<Group>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN)</Group>
-</Authors>
-<Citation>Eur. J. Biochem. 138, 9-37, 1984</Citation>
-<Title>Nomenclature and symbolism for amino acids and peptides. Recommendations 1983.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1984.tb07877.x</Xref>
-<Xref>PMID:6692818</Xref>
-<Note>standard three-letter and one-letter symbols, and nomenclature</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lusty, C.J.</Author>
-<Author>Ratner, S.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 84, 3176-3180, 1987</Citation>
-<Title>Reaction of argininosuccinase with bromomesaconic acid: role of an essential lysine in the active site.</Title>
-<Xref>DOI:10.1073/pnas.84.10.3176</Xref>
-<Xref>PMID:3106962</Xref>
-</ReferenceBlock>
-<Comment>Some active site lysines may form transient covalent bonds with substrates that are not distinguished in the protein sequence database features.</Comment>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Abbreviation>Lys</Abbreviation>
-<Xref>PSI-MOD:00021</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="act_site____k">ACT_SITE</Feature>
-<Feature type="UniProt" key="act_site__schiff-base intermediate with substrate__k">ACT_SITE Schiff-base intermediate with substrate</Feature>
-</Features>
-<Image src="/images/AA0012.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0012.PDB" />
-</Entry>
-<Entry id="AA0013">
-<Header>
-<Code>AA0013</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>25-Feb-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-methionine</Name>
-<AlternateName>2-amino-4-(methylthio)butanoic acid</AlternateName>
-<AlternateName>2-amino-4-(methylthio)butyric acid</AlternateName>
-<AlternateName>2-azanyl-4-(methylsulfanyl)butanoic acid</AlternateName>
-<AlternateName>alpha-amino-gamma-methylmercaptobutyric acid</AlternateName>
-<AlternateName>alpha-amino-gamma-methylthiobutyric acid</AlternateName>
-<AlternateName>gamma-methylthio-alpha-aminobutyric acid</AlternateName>
-<AlternateName>L-(-)-methionine</AlternateName>
-<AlternateName>S-methyl-L-homocysteine</AlternateName>
-<SystematicName>(2S)-2-amino-4-(methylsulfanyl)butanoic acid</SystematicName>
-<Xref>CAS:24425-78-3</Xref>
-<Xref>CAS:63-68-3</Xref>
-<Xref>CAS:7005-18-7</Xref>
-<Xref>ChEBI:16044</Xref>
-<Xref>PDBHET:MET</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 9 N 1 O 1 S 1</Formula>
-<Weight type="chemical">131.19</Weight>
-<Weight type="physical">131.040485</Weight>
-</FormulaBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mueller, J.H.</Author>
-</Authors>
-<Citation>Proc. Soc. Exp. Biol. Med. 19, 161-163, 1922</Citation>
-<Title>A new sulphur-containing amino acid isolated from casein.</Title>
-<Note>identification as a hydrolytic product of casein; isolation; chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mueller, J.H.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 56, 157-169, 1923</Citation>
-<Title>A new sulfur-containing amino-acid isolated from the hydrolytic products of protein.</Title>
-<Note>identification as a hydrolytic product of several proteins; isolation; determination of molecular formula</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Barger, G.</Author>
-<Author>Coyne, F.P.</Author>
-</Authors>
-<Citation>Biochem. J. 22, 1417-1425, 1928</Citation>
-<Title>CLXXVI. The amino-acid methionine; constitution and synthesis.</Title>
-<Xref>PMID:16744158</Xref>
-<Note>determination of structure by synthesis; naming</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fowler, A.V.</Author>
-<Author>Smith, P.J.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 258, 10204-10207, 1983</Citation>
-<Title>The active site regions of lacZ and ebg beta-galactosidases are homologous.</Title>
-<Xref>PMID:6411710</Xref>
-<Note>chemical modification of an active site methionine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Anonymous />
-<Group>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN)</Group>
-</Authors>
-<Citation>Eur. J. Biochem. 138, 9-37, 1984</Citation>
-<Title>Nomenclature and symbolism for amino acids and peptides. Recommendations 1983.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1984.tb07877.x</Xref>
-<Xref>PMID:6692818</Xref>
-<Note>standard three-letter and one-letter symbols, and nomenclature</Note>
-</ReferenceBlock>
-<Comment>Although appropriate, the keyword "thioether bond" normally does not appear for this amino acid, except for certain active site feature annotations.</Comment>
-<SequenceCode>
-<SequenceSpec>M</SequenceSpec>
-<Abbreviation>Met</Abbreviation>
-<Xref>PSI-MOD:00022</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>*thioether bond</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>UniProt has no active site feature annotations for this residue</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0013.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0013.PDB" />
-</Entry>
-<Entry id="AA0014">
-<Header>
-<Code>AA0014</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Jun-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-phenylalanine</Name>
-<AlternateName>2-azanyl-3-phenylpropanoic acid</AlternateName>
-<AlternateName>alpha-amino-beta-phenylpropionic acid</AlternateName>
-<SystematicName>(2S)-2-amino-3-phenylpropanoic acid</SystematicName>
-<Xref>CAS:63-91-2</Xref>
-<Xref>ChEBI:29997</Xref>
-<Xref>PDBHET:PHE</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 9 N 1 O 1</Formula>
-<Weight type="chemical">147.18</Weight>
-<Weight type="physical">147.068414</Weight>
-</FormulaBlock>
-<ReferenceBlock>
-<Authors>
-<Anonymous />
-<Group>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN)</Group>
-</Authors>
-<Citation>Eur. J. Biochem. 138, 9-37, 1984</Citation>
-<Title>Nomenclature and symbolism for amino acids and peptides. Recommendations 1983.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1984.tb07877.x</Xref>
-<Xref>PMID:6692818</Xref>
-<Note>standard three-letter and one-letter symbols, and nomenclature</Note>
-</ReferenceBlock>
-<Comment>Phenylalanine has not been demonstrated to act as active site residue.</Comment>
-<SequenceCode>
-<SequenceSpec>F</SequenceSpec>
-<Abbreviation>Phe</Abbreviation>
-<Xref>PSI-MOD:00023</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>UniProt has no active site feature annotations for this residue</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0014.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0014.PDB" />
-</Entry>
-<Entry id="AA0015">
-<Header>
-<Code>AA0015</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Sep-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-proline</Name>
-<AlternateName>pyrrolidine-2-carboxylic acid</AlternateName>
-<SystematicName>(2S)-2-pyrrolidinecarboxylic acid</SystematicName>
-<Xref>CAS:147-85-3</Xref>
-<Xref>ChEBI:50342</Xref>
-<Xref>PDBHET:PRO</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 7 N 1 O 1</Formula>
-<Weight type="chemical">97.12</Weight>
-<Weight type="physical">97.052764</Weight>
-</FormulaBlock>
-<ReferenceBlock>
-<Authors>
-<Anonymous />
-<Group>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN)</Group>
-</Authors>
-<Citation>Eur. J. Biochem. 138, 9-37, 1984</Citation>
-<Title>Nomenclature and symbolism for amino acids and peptides. Recommendations 1983.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1984.tb07877.x</Xref>
-<Xref>PMID:6692818</Xref>
-<Note>standard three-letter and one-letter symbols, and nomenclature</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Subramanya, H.S.</Author>
-<Author>Roper, D.I.</Author>
-<Author>Dauter, Z.</Author>
-<Author>Dodson, E.J.</Author>
-<Author>Davies, G.J.</Author>
-<Author>Wilson, K.S.</Author>
-<Author>Wigley, D.B.</Author>
-</Authors>
-<Citation>Biochemistry 35, 792-802, 1996</Citation>
-<Title>Enzymatic ketonization of 2-hydroxymuconate: specificity and mechanism investigated by the crystal structures of two isomerases.</Title>
-<Xref>DOI:10.1021/bi951732k</Xref>
-<Xref>PMID:8547259</Xref>
-<Note>evidence for amino-terminal proline active site</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>P</SequenceSpec>
-<Abbreviation>Pro</Abbreviation>
-<Xref>PSI-MOD:00024</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="act_site__proton acceptor; via carboxylate__p">ACT_SITE Proton acceptor; via carboxylate</Feature>
-<Feature type="UniProt" key="act_site__proton acceptor; via imino nitrogen__p">ACT_SITE Proton acceptor; via imino nitrogen</Feature>
-</Features>
-<Image src="/images/AA0015.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0015.PDB" />
-</Entry>
-<Entry id="AA0016">
-<Header>
-<Code>AA0016</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Jun-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-serine</Name>
-<AlternateName>2-azanyl-3-hydroxypropanoic acid</AlternateName>
-<AlternateName>3-hydroxy-L-alanine</AlternateName>
-<AlternateName>alpha-amino-beta-hydroxypropionic acid</AlternateName>
-<AlternateName>beta-hydroxyalanine</AlternateName>
-<SystematicName>(2S)-2-amino-3-hydroxypropanoic acid</SystematicName>
-<Xref>CAS:56-45-1</Xref>
-<Xref>ChEBI:29999</Xref>
-<Xref>PDBHET:SER</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 5 N 1 O 2</Formula>
-<Weight type="chemical">87.08</Weight>
-<Weight type="physical">87.032028</Weight>
-</FormulaBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Birktoft, J.J.</Author>
-<Author>Blow, D.M.</Author>
-<Author>Henderson, R.</Author>
-<Author>Steitz, T.A.</Author>
-</Authors>
-<Citation>Philos. Trans. R. Soc. Lond., B, Biol. Sci. 257, 67-76, 1970</Citation>
-<Title>I. Serine proteinases. The structure of alpha-chymotrypsin.</Title>
-<Xref>PMID:4399050</Xref>
-<Note>X-ray diffraction</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Anonymous />
-<Group>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN)</Group>
-</Authors>
-<Citation>Eur. J. Biochem. 138, 9-37, 1984</Citation>
-<Title>Nomenclature and symbolism for amino acids and peptides. Recommendations 1983.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1984.tb07877.x</Xref>
-<Xref>PMID:6692818</Xref>
-<Note>standard three-letter and one-letter symbols, and nomenclature</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Abbreviation>Ser</Abbreviation>
-<Xref>PSI-MOD:00025</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="act_site____s">ACT_SITE</Feature>
-</Features>
-<Image src="/images/AA0016.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0016.PDB" />
-</Entry>
-<Entry id="AA0017">
-<Header>
-<Code>AA0017</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-Dec-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-threonine</Name>
-<AlternateName>2-azanyl-3-hydroxybutanoic acid</AlternateName>
-<AlternateName>alpha-amino-beta-hydroxybutyric acid</AlternateName>
-<AlternateName>beta-methylserine</AlternateName>
-<AlternateName>L-threo-threonine</AlternateName>
-<SystematicName>(2S,3R)-2-amino-3-hydroxybutanoic acid</SystematicName>
-<Xref>CAS:72-19-5</Xref>
-<Xref>ChEBI:30013</Xref>
-<Xref>PDBHET:THR</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 7 N 1 O 2</Formula>
-<Weight type="chemical">101.10</Weight>
-<Weight type="physical">101.047678</Weight>
-</FormulaBlock>
-<ReferenceBlock>
-<Authors>
-<Author>McCoy, R.E.</Author>
-<Author>Meyer, C.E.</Author>
-<Author>Rose, W.C.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 112, 283-302, 1935</Citation>
-<Title>Feeding experiments with mixtures of highly purified amino acids. VIII. Isolation and identificaton of a new essential amino acid.</Title>
-<Note>identification as an essential dietary amino acid; isolation, purification and structure determination</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Meyer, C.E.</Author>
-<Author>Rose, W.C.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 115, 721-729, 1936</Citation>
-<Title>The spatial configuration of alpha-amino-beta-hydroxy-n-butyric acid.</Title>
-<Note>relative stereochemical determination; naming for stereochemical relationship to D-threose</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Anonymous />
-<Group>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN)</Group>
-</Authors>
-<Citation>Eur. J. Biochem. 138, 9-37, 1984</Citation>
-<Title>Nomenclature and symbolism for amino acids and peptides. Recommendations 1983.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1984.tb07877.x</Xref>
-<Xref>PMID:6692818</Xref>
-<Note>standard three-letter and one-letter symbols, and nomenclature</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Culp, J.S.</Author>
-<Author>Blytt, H.J.</Author>
-<Author>Hermodson, M.</Author>
-<Author>Butler, L.G.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 260, 8320-8324, 1985</Citation>
-<Title>Amino acid sequence of the active site peptide of bovine intestinal 5'-nucleotide phosphodiesterase and identification of the active site residue as threonine.</Title>
-<Xref>PMID:2989287</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Simoni, R.D.</Author>
-<Author>Hill, R.L.</Author>
-<Author>Vaughan, M.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 277, E25, 2002</Citation>
-<Title>The discovery of the amino acid threonine: the work of William C. Rose.</Title>
-<Xref>PMID:12218068</Xref>
-<Note>historical review</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>T</SequenceSpec>
-<Abbreviation>Thr</Abbreviation>
-<Xref>PSI-MOD:00026</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="act_site____t">ACT_SITE</Feature>
-</Features>
-<Image src="/images/AA0017.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0017.PDB" />
-</Entry>
-<Entry id="AA0018">
-<Header>
-<Code>AA0018</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>25-Feb-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-tryptophan</Name>
-<AlternateName>2-azanyl-3-(1H-indol-3-yl)propanoic acid</AlternateName>
-<AlternateName>alpha-amino-beta-(3-indolyl)propionoic acid</AlternateName>
-<AlternateName>beta(3-indolyl)alanine</AlternateName>
-<SystematicName>(2S)-2-amino-3-(1H-indol-3-yl)propanoic acid</SystematicName>
-<Xref>CAS:73-22-3</Xref>
-<Xref>ChEBI:29954</Xref>
-<Xref>PDBHET:TRP</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 11 H 10 N 2 O 1</Formula>
-<Weight type="chemical">186.21</Weight>
-<Weight type="physical">186.079313</Weight>
-</FormulaBlock>
-<ReferenceBlock>
-<Authors>
-<Anonymous />
-<Group>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN)</Group>
-</Authors>
-<Citation>Eur. J. Biochem. 138, 9-37, 1984</Citation>
-<Title>Nomenclature and symbolism for amino acids and peptides. Recommendations 1983.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1984.tb07877.x</Xref>
-<Xref>PMID:6692818</Xref>
-<Note>standard three-letter and one-letter symbols, and nomenclature</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Li, Y.F.</Author>
-<Author>Heelis, P.F.</Author>
-<Author>Sancar, A.</Author>
-</Authors>
-<Citation>Biochemistry 30, 6322-6329, 1991</Citation>
-<Title>Active site of DNA photolyase: tryptophan-306 is the intrinsic hydrogen atom donor essential for flavin radical photoreduction and DNA repair in vitro.</Title>
-<Xref>DOI:10.1021/bi00239a034</Xref>
-<Xref>PMID:2059637</Xref>
-<Note>spectrographic characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Starks, C.M.</Author>
-<Author>Back, K.</Author>
-<Author>Chappell, J.</Author>
-<Author>Noel, J.P.</Author>
-</Authors>
-<Citation>Science 277, 1815-1820, 1997</Citation>
-<Title>Structural basis for cyclic terpene biosynthesis by tobacco 5-epi-aristolochene synthase.</Title>
-<Xref>DOI:10.1126/science.277.5333.1815</Xref>
-<Xref>PMID:9295271</Xref>
-<Note>a protonated tryptophan cation active site is proposed</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>W</SequenceSpec>
-<Abbreviation>Trp</Abbreviation>
-<Xref>PSI-MOD:00027</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="act_site__tryptophan radical intermediate__w">ACT_SITE Tryptophan radical intermediate</Feature>
-<Feature type="UniProt" key="site__electron transfer via tryptophanyl radical__w">SITE Electron transfer via tryptophanyl radical</Feature>
-</Features>
-<Image src="/images/AA0018.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0018.PDB" />
-</Entry>
-<Entry id="AA0019">
-<Header>
-<Code>AA0019</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Sep-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-tyrosine</Name>
-<AlternateName>2-azanyl-3-(4-hydoxyphenyl)propanoic acid</AlternateName>
-<AlternateName>alpha-amino-beta-(para-hydroxyphenyl)propionic acid</AlternateName>
-<AlternateName>p-tyrosine</AlternateName>
-<AlternateName>para-hydroxyphenylalanine</AlternateName>
-<SystematicName>(2S)-2-amino-3-(4-hydoxyphenyl)propanoic acid</SystematicName>
-<Xref>CAS:60-18-4</Xref>
-<Xref>ChEBI:46858</Xref>
-<Xref>PDBHET:TYR</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 9 N 1 O 2</Formula>
-<Weight type="chemical">163.18</Weight>
-<Weight type="physical">163.063329</Weight>
-</FormulaBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Takahashi, K.</Author>
-<Author>Stein, W.H.</Author>
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-</Authors>
-<Citation>J. Biol. Chem. 242, 4682-4690, 1967</Citation>
-<Title>The identification of a glutamic acid residue as part of the active site of ribonuclease T-1.</Title>
-<Xref>PMID:6061414</Xref>
-</ReferenceBlock>
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-</Authors>
-<Citation>J. Biochem. 69, 331-338, 1971</Citation>
-<Title>The structure and function of ribonuclese T-1. XII. Further studies on rose bengal-catalyzed photooxidation of ribonuclease T-1- identification of a critical histidine residue.</Title>
-<Xref>PMID:5550972</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Swenson, R.P.</Author>
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-<Author>Massey, V.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 257, 1937-1944, 1982</Citation>
-<Title>Chemical modification of D-amino acid oxidase. Amino acid sequence of the tryptic peptides containing tyrosine and lysine residues modified by fluorodinitrobenzene.</Title>
-<Xref>PMID:6120171</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Anonymous />
-<Group>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN)</Group>
-</Authors>
-<Citation>Eur. J. Biochem. 138, 9-37, 1984</Citation>
-<Title>Nomenclature and symbolism for amino acids and peptides. Recommendations 1983.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1984.tb07877.x</Xref>
-<Xref>PMID:6692818</Xref>
-<Note>standard three-letter and one-letter symbols, and nomenclature</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lynn, R.M.</Author>
-<Author>Bjornsti, M.A.</Author>
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-<Author>Wang, J.C.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 86, 3559-3563, 1989</Citation>
-<Title>Peptide sequencing and site-directed mutagenesis identify tyrosine-727 as the active site tyrosine of Saccharomyces cerevisiae DNA topoisomerase I.</Title>
-<Xref>DOI:10.1073/pnas.86.10.3559</Xref>
-<Xref>PMID:2542938</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Nordlund, P.</Author>
-<Author>Sjoeberg, B.M.</Author>
-<Author>Eklund, H.</Author>
-</Authors>
-<Citation>Nature 345, 593-598, 1990</Citation>
-<Title>Three-dimensional structure of the free radical protein of ribonucleotide reductase.</Title>
-<Xref>DOI:10.1038/345593a0</Xref>
-<Xref>PMID:2190093</Xref>
-<Note>X-ray diffraction</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>Y</SequenceSpec>
-<Abbreviation>Tyr</Abbreviation>
-<Xref>PSI-MOD:00028</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="act_site____y">ACT_SITE</Feature>
-</Features>
-<Image src="/images/AA0019.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0019.PDB" />
-</Entry>
-<Entry id="AA0020">
-<Header>
-<Code>AA0020</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Jun-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-valine</Name>
-<AlternateName>2-azanyl-3-methylbutanoic acid</AlternateName>
-<AlternateName>alpha-amino-beta-methylbutyric acid</AlternateName>
-<AlternateName>alpha-aminoisovaleric acid</AlternateName>
-<SystematicName>(2S)-2-amino-3-methylbutanoic acid</SystematicName>
-<Xref>CAS:72-18-4</Xref>
-<Xref>ChEBI:30015</Xref>
-<Xref>PDBHET:VAL</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 9 N 1 O 1</Formula>
-<Weight type="chemical">99.13</Weight>
-<Weight type="physical">99.068414</Weight>
-</FormulaBlock>
-<ReferenceBlock>
-<Authors>
-<Anonymous />
-<Group>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN)</Group>
-</Authors>
-<Citation>Eur. J. Biochem. 138, 9-37, 1984</Citation>
-<Title>Nomenclature and symbolism for amino acids and peptides. Recommendations 1983.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1984.tb07877.x</Xref>
-<Xref>PMID:6692818</Xref>
-<Note>standard three-letter and one-letter symbols, and nomenclature</Note>
-</ReferenceBlock>
-<Comment>The alpha carboxyl group of a C-terminal valine is predicted to act as a proton acceptor in the active site of an enzyme.</Comment>
-<SequenceCode>
-<SequenceSpec>V</SequenceSpec>
-<Abbreviation>Val</Abbreviation>
-<Xref>PSI-MOD:00029</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="act_site__proton acceptor; via carboxylate__v">ACT_SITE Proton acceptor; via carboxylate</Feature>
-</Features>
-<Image src="/images/AA0020.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0020.PDB" />
-</Entry>
-<Entry id="AA0021">
-<Header>
-<Code>AA0021</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-formyl-L-methionine</Name>
-<AlternateName>2-formamido-4-(methylsulfanyl)butanoic acid</AlternateName>
-<AlternateName>2-formylamino-4-(methylthio)butanoic acid</AlternateName>
-<AlternateName>2-formylazanyl-4-(methylsulfanyl)butanoic acid</AlternateName>
-<SystematicName>(2S)-2-formylamino-4-(methylsulfanyl)butanoic acid</SystematicName>
-<Xref>CAS:4289-98-9</Xref>
-<Xref>ChEBI:49298</Xref>
-<Xref>PDBHET:FME</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 10 N 1 O 2 S 1</Formula>
-<Weight type="chemical">160.21</Weight>
-<Weight type="physical">160.043225</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0021" label="FMET">
-<Formula>C 0 H 0 N 0 O 0 S 0</Formula>
-<Weight type="chemical">0.00</Weight>
-<Weight type="physical">0.000000</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0013" label="MET">
-<Formula>C 1 H 0 N 0 O 1 S 0</Formula>
-<Weight type="chemical">28.01</Weight>
-<Weight type="physical">27.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Adams, J.M.</Author>
-<Author>Capecchi, M.R.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 55, 147-155, 1966</Citation>
-<Title>N-formylmethionyl-sRNA as the initiator of protein synthesis.</Title>
-<Xref>DOI:10.1073/pnas.55.1.147</Xref>
-<Xref>PMID:5328638</Xref>
-<Note>identification of N-formylmethionyl-tRNA as necessary for the initiation of protein synthesis in Escherichia coli</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Webster, R.E.</Author>
-<Author>Engelhardt, D.L.</Author>
-<Author>Zinder, N.D.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 55, 155-161, 1966</Citation>
-<Title>In vitro protein synthesis: chain initiation.</Title>
-<Xref>DOI:10.1073/pnas.55.1.155</Xref>
-<Xref>PMID:5220863</Xref>
-<Note>identification of N-formylmethionine as the blocked N-terminal of phage coat protein synthesized by Escherichia coli</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
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-</Authors>
-<Citation>Science 153, 416-418, 1966</Citation>
-<Title>Formylmethionine codon AUG as an initiator of polypeptide synthesis.</Title>
-<Xref>DOI:10.1126/science.153.3734.416</Xref>
-<Xref>PMID:5328567</Xref>
-<Note>determination that the AUG codon was translated by the N-formylmethionyl-tRNA during the initiation of protein synthesis in Escherichia coli</Note>
-</ReferenceBlock>
-<ReferenceBlock>
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-</Authors>
-<Citation>Acta Crystallogr. B 33, 3332-3336, 1977</Citation>
-<Title>Structure and conformation of amino acids containing sulfur. V. N-Formyl-L-methionine.</Title>
-<Xref>DOI:10.1107/S0567740877010942</Xref>
-<Note>X-ray diffraction</Note>
-</ReferenceBlock>
-<ReferenceBlock>
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-</Authors>
-<Citation>J. Biol. Chem. 263, 11516-11522, 1988</Citation>
-<Title>Structural characterization of Escherichia coli phosphatidylserine decarboxylase.</Title>
-<Xref>PMID:3042771</Xref>
-<Note>identification and removal of formyl group using 25% trifluoroacetic acid</Note>
-</ReferenceBlock>
-<ReferenceBlock>
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-</Authors>
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-<Note>HPLC identification of N-formylhomoserine; N-formylmethionine initiates protein synthesis on vertebrate mitochondrial ribosomes</Note>
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-<Xref>PMID:9159480</Xref>
-<Note>X-ray diffraction, 2.50 angstroms; an N-formyl carbonyl group axially ligates the magnesium ion of bacteriochlorophyll a in light-harvesting protein B-800/850 alpha chain; it is probably the hydrated form, N-(dihydroxymethyl)methionine</Note>
-</ReferenceBlock>
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-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, August 1996</Citation>
-<Description>Integral membrane peripheral light harvesting complex from Rhodopseudomonas acidophila strain 10050.</Description>
-<Xref>PDB:1KZU</Xref>
-<Note>X-ray diffraction, 2.50 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
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-<Note>mass spectrometric identification of N-formyl-methionine; deformylation with acetyl chloride</Note>
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-<Xref>PMID:12054867</Xref>
-<Note>N-formylmethionine detected by mass spectrometry; authors' initials in the PubMed citation are corrected</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Walker, J.E.</Author>
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-<Xref>PMID:19348885</Xref>
-<Note>top-down mass-spectrometry; all of 13 proteins encoded in bovine mitochondrial DNA retain the N-formylmethionine initiator except cytochrome c oxidase subunit 3 which undergoes partial processing to remove the formyl group or the N-formylmethionine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Tucker, E.J.</Author>
-<Author>Hershman, S.G.</Author>
-<Author>Köhrer, C.</Author>
-<Author>Belcher-Timme, C.A.</Author>
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-<Author>Goldberger, O.A.</Author>
-<Author>Christodoulou, J.</Author>
-<Author>Silberstein, J.M.</Author>
-<Author>McKenzie, M.</Author>
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-<Author>Compton, A.G.</Author>
-<Author>Jaffe, J.D.</Author>
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-<Author>Calvo, S.E.</Author>
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-</Authors>
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-<Title>Mutations in MTFMT underlie a human disorder of formylation causing impaired mitochondrial translation.</Title>
-<Xref>DOI:10.1016/j.cmet.2011.07.010</Xref>
-<Xref>PMID:21907147</Xref>
-<Note>mutations in the gene for human methionyl-tRNA formyltransferase can cause combined severe oxidative phosphorylation deficiency by impairing mitochondrial protein synthesis</Note>
-</ReferenceBlock>
-<Comment>N-formylmethionine is translated for the initiator codon in bacteria, and there are different tRNA's with specific tRNA synthases for the initiator N-formylmethionine and the elongation methionine forms.</Comment>
-<Comment>In eukaryotic organelles there is only one tRNA for methionine. A portion of the Met-tRNA is N-formylated by mitochondrion specific methionyl-tRNA formyltransferase and recruited by mitochondrial translation initiation factor 2.</Comment>
-<Comment>As an aldehyde, the formyl group readily undergoes hydration. For the hydrated form N-(dihydroxymethyl)-L-methionine of this residue, see RESID:AA0493.</Comment>
-<Comment>Although appropriate, the keyword "thioether bond" normally does not appear for this amino acid.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>methionine--tRNA ligase (EC 6.1.1.10)</EnzymeName>
-<EnzymeName>methionyl-tRNA formyltransferase (EC 2.1.2.9)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode link="FMET">
-<SequenceSpec>M</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>PSI-MOD:00030</Xref>
-</SequenceCode>
-<SequenceCode link="MET">
-<SequenceSpec>M</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>PSI-MOD:00482</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>*thioether bond</Keyword>
-<Keyword>blocked amino end</Keyword>
-<Keyword>formylation</Keyword>
-<Keyword>pretranslational modification</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n-formylmethionine__m">MOD_RES N-formylmethionine</Feature>
-</Features>
-<Image src="/images/AA0021.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0021.PDB" />
-</Entry>
-<Entry id="AA0022">
-<Header>
-<Code>AA0022</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-selenocysteine</Name>
-<AlternateName>2-azanyl-3-selanylpropanoic acid</AlternateName>
-<AlternateName>3-selenylalanine</AlternateName>
-<AlternateName>SeCys</AlternateName>
-<AlternateName>selenium cysteine</AlternateName>
-<SystematicName>(2R)-2-amino-3-selanylpropanoic acid</SystematicName>
-<Xref>CAS:10236-58-5</Xref>
-<Xref>ChEBI:30000</Xref>
-<Xref>PDBHET:CSE</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 5 N 1 O 1 Se 1</Formula>
-<Weight type="chemical">150.05</Weight>
-<Weight type="physical">150.953635</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0022" label="SEC">
-<Formula>C 0 H 0 N 0 O 0 Se 0</Formula>
-<Weight type="chemical">0.00</Weight>
-<Weight type="physical">0.000000</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0005" label="CYS">
-<Formula>C 0 H 0 N 0 O 0 S -1 Se 1</Formula>
-<Weight type="chemical">46.91</Weight>
-<Weight type="physical">47.944450</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Huber, R.E.</Author>
-<Author>Criddle, R.S.</Author>
-</Authors>
-<Citation>Arch. Biochem. Biophys. 122, 164-173, 1967</Citation>
-<Title>Comparison of the chemical properties of selenocysteine and selenocystine with their sulfur analogs.</Title>
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-</ReferenceBlock>
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-</Authors>
-<Citation>Arch. Biochem. Biophys. 154, 366-381, 1973</Citation>
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-</Authors>
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-<Xref>DOI:10.1126/science.1068186</Xref>
-<Xref>PMID:11884747</Xref>
-<Note>X-ray diffraction, 1.6 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Jormakka, M.</Author>
-<Author>Tornroth, S.</Author>
-<Author>Byrne, B.</Author>
-<Author>Iwata, S.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, January 2002</Citation>
-<Description>Formate dehydrogenase N from E. coli.</Description>
-<Xref>PDB:1KQF</Xref>
-<Note>X-ray diffraction, 1.60 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Itoh, Y.</Author>
-<Author>Bröcker, M.J.</Author>
-<Author>Sekine, S.</Author>
-<Author>Hammond, G.</Author>
-<Author>Suetsugu, S.</Author>
-<Author>Söll, D.</Author>
-<Author>Yokoyama, S.</Author>
-</Authors>
-<Citation>Science 340, 75-78, 2013</Citation>
-<Title>Decameric SelA.tRNA(Sec) ring structure reveals mechanism of bacterial selenocysteine formation.</Title>
-<Xref>DOI:10.1126/science.1229521</Xref>
-<Xref>PMID:23559248</Xref>
-<Note>in bacteria selenocysteine is produced by serine acylation to tRNA(Sec) followed by reaction with selenophosphate to form selenocysteinyl-tRNA(Sec)</Note>
-</ReferenceBlock>
-<Comment>Selenocysteine is translated for the UGA codon in some genetic systems. It has not yet been demonstrated to arise alternatively from a post-translational modification.</Comment>
-<Comment>Although the single letter symbol U is recommended by IUBMB, many software applications fail to recognize it, and some sequence databases may use the single letter symbol C.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>serine--tRNA ligase (EC 6.1.1.11)</EnzymeName>
-<EnzymeName>L-seryl-tRNA(Sec) selenium transferase, SelA (EC 2.9.1.1)</EnzymeName>
-<EnzymeName>O-phosphoseryl-tRNA(Sec) kinase (EC 2.7.1.164)</EnzymeName>
-<EnzymeName>O-phospho-L-seryl-tRNA(Sec):L-selenocysteinyl-tRNA synthase, SepSecS (EC 2.9.1.2)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode link="SEC">
-<SequenceSpec>U</SequenceSpec>
-<Abbreviation>Sec</Abbreviation>
-<Xref>GO:0001514</Xref>
-<Xref>PSI-MOD:00031</Xref>
-</SequenceCode>
-<SequenceCode link="CYS">
-<SequenceSpec>C</SequenceSpec>
-<Xref>PSI-MOD:00686</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>pretranslational modification</Keyword>
-<Keyword>selenium</Keyword>
-<Keyword>selenocysteine</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="non_std__selenocysteine__u">NON_STD Selenocysteine</Feature>
-</Features>
-<Image src="/images/AA0022.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0022.PDB" />
-</Entry>
-<Entry id="AA0023">
-<Header>
-<Code>AA0023</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Apr-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-aspartic acid or L-asparagine</Name>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 5 N 1 O 3, C 4 H 6 N 2 O 2</Formula>
-<Weight type="chemical">115.09, 114.10</Weight>
-<Weight type="physical">115.026943, 114.042927</Weight>
-</FormulaBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Airoldi, L.P.</Author>
-<Author>Doonan, S.</Author>
-</Authors>
-<Citation>FEBS Lett. 50, 155-158, 1975</Citation>
-<Title>A method of distinguishing between aspartic acid and asparagine and between glutamic acid and glutamine during sequence analysis by the dansyl-Edman procedure.</Title>
-<Xref>DOI:10.1016/0014-5793(75)80478-9</Xref>
-<Xref>PMID:1089562</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Anonymous />
-<Group>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN)</Group>
-</Authors>
-<Citation>Eur. J. Biochem. 138, 9-37, 1984</Citation>
-<Title>Nomenclature and symbolism for amino acids and peptides. Recommendations 1983.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1984.tb07877.x</Xref>
-<Xref>PMID:6692818</Xref>
-<Note>standard three-letter and one-letter symbols, and nomenclature</Note>
-</ReferenceBlock>
-<Comment>This represents an uncertain amidation of an aspartic acid.</Comment>
-<SequenceCode>
-<SequenceSpec>B</SequenceSpec>
-<Abbreviation>Asx</Abbreviation>
-</SequenceCode>
-<Source>ambiguity</Source>
-<Image src="/images/AA0023.GIF" alt="DUMMY.GIF" />
-</Entry>
-<Entry id="AA0024">
-<Header>
-<Code>AA0024</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Apr-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-glutamic acid or L-glutamine</Name>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 7 N 1 O 3, C 5 H 8 N 2 O 2</Formula>
-<Weight type="chemical">129.11, 128.13</Weight>
-<Weight type="physical">129.042593, 128.058578</Weight>
-</FormulaBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Airoldi, L.P.</Author>
-<Author>Doonan, S.</Author>
-</Authors>
-<Citation>FEBS Lett. 50, 155-158, 1975</Citation>
-<Title>A method of distinguishing between aspartic acid and asparagine and between glutamic acid and glutamine during sequence analysis by the dansyl-Edman procedure.</Title>
-<Xref>DOI:10.1016/0014-5793(75)80478-9</Xref>
-<Xref>PMID:1089562</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Anonymous />
-<Group>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN)</Group>
-</Authors>
-<Citation>Eur. J. Biochem. 138, 9-37, 1984</Citation>
-<Title>Nomenclature and symbolism for amino acids and peptides. Recommendations 1983.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1984.tb07877.x</Xref>
-<Xref>PMID:6692818</Xref>
-<Note>standard three-letter and one-letter symbols, and nomenclature</Note>
-</ReferenceBlock>
-<Comment>This represents an uncertain amidation of a glutamic acid.</Comment>
-<SequenceCode>
-<SequenceSpec>Z</SequenceSpec>
-<Abbreviation>Glx</Abbreviation>
-</SequenceCode>
-<Source>ambiguity</Source>
-<Image src="/images/AA0024.GIF" alt="DUMMY.GIF" />
-</Entry>
-<Entry id="AA0025">
-<Header>
-<Code>AA0025</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-cystine</Name>
-<AlternateName>2-amino-3-(2-amino-2-carboxy-ethyl)disulfanyl-propanoic acid [misnomer]</AlternateName>
-<AlternateName>3,3'-disulfane-1,2-diylbis(2-azanylpropanoic acid)</AlternateName>
-<AlternateName>3,3'-dithiobis(2-aminopropanoic acid)</AlternateName>
-<AlternateName>3,3'-dithiobisalanine</AlternateName>
-<AlternateName>3,3'-dithiodialanine</AlternateName>
-<AlternateName>beta,beta'-diamino-beta,beta'-dicarboxydiethyldisulfide</AlternateName>
-<AlternateName>beta,beta'-dithiodialanine</AlternateName>
-<AlternateName>bis(alpha-aminopropionic acid)-beta-disulfide</AlternateName>
-<AlternateName>bis(beta-amino-beta-carboxyethyl)disulfide</AlternateName>
-<AlternateName>dicysteine</AlternateName>
-<SystematicName>(2R,2'R)-3,3'-disulfane-1,2-diylbis(2-aminopropanoic acid)</SystematicName>
-<Xref>CAS:56-89-3</Xref>
-<Xref>ChEBI:50058</Xref>
-<Xref>PDBHET:CYS</Xref>
-</Names>
-<FormulaBlock label="CYS2">
-<Formula>C 6 H 8 N 2 O 2 S 2</Formula>
-<Weight type="chemical">204.26</Weight>
-<Weight type="physical">204.002720</Weight>
-</FormulaBlock>
-<FormulaBlock label="CYS1">
-<Formula>C 6 H 10 N 2 O 3 S 2</Formula>
-<Weight type="chemical">222.28</Weight>
-<Weight type="physical">222.013284</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005" link="CYS2">
-<Formula>C 0 H -2 N 0 O 0 S 0</Formula>
-<Weight type="chemical">-2.02</Weight>
-<Weight type="physical">-2.015650</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0005" link="CYS1">
-<Formula>C 3 H 5 N 1 O 2 S 1</Formula>
-<Weight type="chemical">119.14</Weight>
-<Weight type="physical">119.004099</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Soderberg, B.O.</Author>
-<Author>Sjoberg, B.M.</Author>
-<Author>Sonnerstam, U.</Author>
-<Author>Branden, C.I.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 75, 5827-5830, 1978</Citation>
-<Title>Three-dimensional structure of thioredoxin induced by bacteriophage T4.</Title>
-<Xref>DOI:10.1073/pnas.75.12.5827</Xref>
-<Xref>PMID:366603</Xref>
-<Note>X-ray diffraction, 2.8 angstroms; redox-active disulfide bond</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bergenhem, N.</Author>
-<Author>Carlsson, U.</Author>
-<Author>Strid, L.</Author>
-</Authors>
-<Citation>Biochim. Biophys. Acta 871, 55-60, 1986</Citation>
-<Title>The existence of glutathione and cysteine disulfide-linked to erythrocyte carbonic anhydrase from tiger shark.</Title>
-<Xref>DOI:10.1016/0167-4838(86)90132-9</Xref>
-<Xref>PMID:3083866</Xref>
-<Note>chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sørensen, H.H.</Author>
-<Author>Thomsen, J.</Author>
-<Author>Bayne, S.</Author>
-<Author>Højrup, P.</Author>
-<Author>Roepstorff, P.</Author>
-</Authors>
-<Citation>Biomed. Environ. Mass Spectrom. 19, 713-720, 1990</Citation>
-<Title>Strategies for determination of disulphide bridges in proteins using plasma desorption mass spectrometry.</Title>
-<Xref>DOI:10.1002/bms.1200191110</Xref>
-<Xref>PMID:2076469</Xref>
-<Note>the spellings of "Sorensen, H.H." and "Hojrup, P." in the PubMed citation are corrected</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Balhorn, R.</Author>
-<Author>Corzett, M.</Author>
-<Author>Mazrimas, J.</Author>
-<Author>Watkins, B.</Author>
-</Authors>
-<Citation>Biochemistry 30, 175-181, 1991</Citation>
-<Title>Identification of bull protamine disulfides.</Title>
-<Xref>DOI:10.1021/bi00215a026</Xref>
-<Xref>PMID:1988019</Xref>
-<Note>chemical titration and characterization of disulfide bonds; results from this methodology must be carefully evaluated</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Forman-Kay, J.D.</Author>
-<Author>Clore, G.M.</Author>
-<Author>Wingfield, P.T.</Author>
-<Author>Gronenborn, A.M.</Author>
-</Authors>
-<Citation>Biochemistry 30, 2685-2698, 1991</Citation>
-<Title>High-resolution three-dimensional structure of reduced recombinant human thioredoxin in solution.</Title>
-<Xref>DOI:10.1021/bi00224a017</Xref>
-<Xref>PMID:2001356</Xref>
-<Note>(1)H-NMR and (15)N-NMR analysis; redox-active disulfide bond</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Dörmann, P.</Author>
-<Author>Börchers, T.</Author>
-<Author>Korf, U.</Author>
-<Author>Højrup, P.</Author>
-<Author>Roepstorff, P.</Author>
-<Author>Spener, F.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 268, 16286-16292, 1993</Citation>
-<Title>Amino acid exchange and covalent modification by cysteine and glutathione explain isoforms of fatty acid-binding protein occurring in bovine liver.</Title>
-<Xref>PMID:8344916</Xref>
-<Note>mass spectrometric detection</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yang, C.Y.</Author>
-<Author>Gu, Z.W.</Author>
-<Author>Blanco-Vaca, F.</Author>
-<Author>Gaskell, S.J.</Author>
-<Author>Yang, M.</Author>
-<Author>Massey, J.B.</Author>
-<Author>Gotto Jr., A.M.</Author>
-<Author>Pownall, H.J.</Author>
-</Authors>
-<Citation>Biochemistry 33, 12451-12455, 1994</Citation>
-<Title>Structure of human apolipoprotein D: locations of the intermolecular and intramolecular disulfide links.</Title>
-<Xref>DOI:10.1021/bi00207a011</Xref>
-<Xref>PMID:7918467</Xref>
-<Note>mass spectrometric identification of disulfide bonds</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hadfield, A.</Author>
-<Author>Shammas, C.</Author>
-<Author>Kryger, G.</Author>
-<Author>Ringe, D.</Author>
-<Author>Petsko, G.A.</Author>
-<Author>Ouyang, J.</Author>
-<Author>Viola, R.E.</Author>
-</Authors>
-<Citation>Biochemistry 40, 14475-14483, 2001</Citation>
-<Title>Active site analysis of the potential antimicrobial target aspartate semialdehyde dehydrogenase.</Title>
-<Xref>DOI:10.1021/bi015713o</Xref>
-<Xref>PMID:11724560</Xref>
-<Note>X-ray diffraction, 2.60 angstroms; inhibitor S-methyl cysteine sulfoxide may react with the active site cysteine to form a disulfide bond and release methanol; although not a natural formation of cystine, it is a model for enzymes inhibited by oxidative disulfide formation with free cysteine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hadfield, A.T.</Author>
-<Author>Kryger, G.</Author>
-<Author>Ouyang, J.</Author>
-<Author>Ringe, D.</Author>
-<Author>Petsko, G.A.</Author>
-<Author>Viola, R.E.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, August 2001</Citation>
-<Description>Aspartate beta-semialdehyde dehydrogenase in complex with NADP and substrate analogue S-methyl cysteine sulfoxide.</Description>
-<Xref>PDB:1GL3</Xref>
-<Note>X-ray diffraction, 2.60 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Metanis, N.</Author>
-<Author>Keinan, E.</Author>
-<Author>Dawson, P.E.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 128, 16684-16691, 2006</Citation>
-<Title>Synthetic seleno-glutaredoxin 3 analogues are highly reducing oxidoreductases with enhanced catalytic efficiency.</Title>
-<Xref>DOI:10.1021/ja0661414</Xref>
-<Xref>PMID:17177418</Xref>
-<Note>comparative redox potentials of cystine, cysteinylselenocysteine and selenocystine in synthetic glutaredoxins with a [C/U]XX[C/U] motif</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kolarich, D.</Author>
-<Author>Weber, A.</Author>
-<Author>Turecek, P.L.</Author>
-<Author>Schwarz, H.P.</Author>
-<Author>Altmann, F.</Author>
-</Authors>
-<Citation>Proteomics 6, 3369-3380, 2006</Citation>
-<Title>Comprehensive glyco-proteomic analysis of human alpha1-antitrypsin and its charge isoforms.</Title>
-<Xref>DOI:10.1002/pmic.200500751</Xref>
-<Xref>PMID:16622833</Xref>
-<Note>mass spectrometric determination of cysteine disulfide bonded to peptidyl cysteine</Note>
-</ReferenceBlock>
-<Comment>Most extracellular proteins appear to undergo normal disulfide bond formation spontaneously during secretion. Some proteins require assistance from chaperonins and protein disulfide-isomerase.</Comment>
-<Comment>Binding of free cysteine extracellularly is probably not enzymatically catalyzed.</Comment>
-<Comment>The experimental redox potential of cystine in synthetic glutaredoxin 3 is -194 mV. See RESID:AA0358 and RESID:AA0437.</Comment>
-<Comment>The formula and records labeled "CYS2" refers to cystine produced as a disulfide cross-link of two peptidyl cysteine residues.</Comment>
-<Comment>The formula and records labeled "CYS1" refers to cystine produced as a peptidyl cysteine residue disulfide bonded to a free cysteine.</Comment>
-<GeneratingEnzyme>
-<EnzymeName link="CYS2">protein-disulfide reductase (EC 1.8.1.8)</EnzymeName>
-<EnzymeName link="CYS2">protein disulfide-isomerase (EC 5.3.4.1)</EnzymeName>
-<EnzymeName link="CYS1">autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode link="CYS2">
-<SequenceSpec>C, C</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>GO:0018316</Xref>
-<Xref>PSI-MOD:00034</Xref>
-</SequenceCode>
-<SequenceCode link="CYS1">
-<SequenceSpec>C</SequenceSpec>
-<Xref>PSI-MOD:00765</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>*redox-active center</Keyword>
-<Keyword>disulfide bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="act_site__redox-active__c" link="CYS2">ACT_SITE Redox-active</Feature>
-<Feature type="UniProt" key="disulfid____c__c" link="CYS2">DISULFID</Feature>
-<Feature type="UniProt" key="disulfid__interchain__c" link="CYS2">DISULFID Interchain</Feature>
-<Feature type="UniProt" key="disulfid__interchain (between__c__c" link="CYS2">DISULFID Interchain (between ... chains)</Feature>
-<Feature type="UniProt" key="disulfid__interchain (with__c" link="CYS2">DISULFID Interchain (with C-...)</Feature>
-<Feature type="UniProt" key="disulfid__redox-active__c__c" link="CYS2">DISULFID Redox-active</Feature>
-<Feature type="UniProt" key="mod_res__s-cysteinyl cysteine__c" link="CYS1">MOD_RES S-cysteinyl cysteine</Feature>
-</Features>
-<Image src="/images/AA0025.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0025.PDB" />
-</Entry>
-<Entry id="AA0026">
-<Header>
-<Code>AA0026</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>25-Feb-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>(2S,3R)-3-hydroxyasparagine</Name>
-<AlternateName>(2S,3R)-2,4-diamino-3-hydroxy-4-oxobutanoic acid</AlternateName>
-<AlternateName>2-azanyl-3-hydroxy-4-butanediamic acid</AlternateName>
-<AlternateName>L-erythro-beta-hydroxyasparagine</AlternateName>
-<SystematicName>(2S,3R)-2-amino-3-hydroxy-4-butanediamic acid</SystematicName>
-<Xref>CAS:20790-74-3</Xref>
-<Xref>PDBHET:AHB</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 6 N 2 O 3</Formula>
-<Weight type="chemical">130.10</Weight>
-<Weight type="physical">130.037842</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0003">
-<Formula>C 0 H 0 N 0 O 1</Formula>
-<Weight type="chemical">16.00</Weight>
-<Weight type="physical">15.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Stenflo, J.</Author>
-<Author>Lundwall, A.</Author>
-<Author>Dahlbäck, B.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 84, 368-372, 1987</Citation>
-<Title>beta-Hydroxyasparagine in domains homologous to the epidermal growth factor precursor in vitamin K-dependent protein S.</Title>
-<Xref>DOI:10.1073/pnas.84.2.368</Xref>
-<Xref>PMID:2948188</Xref>
-<Note>chromatographic detection; the stereochemistry was determined by hydrolysis and comparison with "erythro-beta-hydroxyaspartic acid"</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Arlaud, G.J.</Author>
-<Author>Van Dorsselaer, A.</Author>
-<Author>Bell, A.</Author>
-<Author>Mancini, M.</Author>
-<Author>Aude, C.</Author>
-<Author>Gagnon, J.</Author>
-</Authors>
-<Citation>FEBS Lett. 222, 129-134, 1987</Citation>
-<Title>Identification of erythro-beta-hydroxyasparagine in the EGF-like domain of human C1r.</Title>
-<Xref>DOI:10.1016/0014-5793(87)80205-3</Xref>
-<Xref>PMID:2820791</Xref>
-<Note>mass spectrometric detection; the stereochemistry was determined by hydrolysis and comparison with "erythro-beta-hydroxyaspartic acid"</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Feinberg, H.</Author>
-<Author>Uitdehaag, J.C.</Author>
-<Author>Davies, J.M.</Author>
-<Author>Wallis, R.</Author>
-<Author>Drickamer, K.</Author>
-<Author>Weis, W.I.</Author>
-</Authors>
-<Citation>EMBO J. 22, 2348-2359, 2003</Citation>
-<Title>Crystal structure of the CUB1-EGF-CUB2 region of mannose-binding protein associated serine protease-2.</Title>
-<Xref>DOI:10.1093/emboj/cdg236</Xref>
-<Xref>PMID:12743029</Xref>
-<Note>X-ray diffraction, 2.70 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Feinberg, H.</Author>
-<Author>Uitdehaag, J.C.</Author>
-<Author>Davies, J.M.</Author>
-<Author>Wallis, R.</Author>
-<Author>Drickamer, K.</Author>
-<Author>Weis, W.I.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, January 2003</Citation>
-<Description>Crystal structure of the CUB1-EGF-CUB2 region of MASP2 molecule: mannose-binding protein associated serine protease-2.</Description>
-<Xref>PDB:1NT0</Xref>
-<Note>X-ray diffraction, 2.70 angstroms</Note>
-</ReferenceBlock>
-<Comment>This diastereomeric form has been found in the EGF domain of many proteins. For the (2S,3S)-diastereomer, see RESID:AA0478.</Comment>
-<Comment>The PDB group code includes models with both the (2S,3R) and the (2S,3S) stereoconfiguration.</Comment>
-<Comment>The Enzyme Commission has not yet distinguished the different stereospecific enzyme activities.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptide-aspartate beta-dioxygenase (EC 1.14.11.16)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>N</SequenceSpec>
-<Xref>GO:0018376</Xref>
-<Xref>PSI-MOD:00035</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__(3r)-3-hydroxyasparagine__n">MOD_RES (3R)-3-hydroxyasparagine</Feature>
-</Features>
-<Image src="/images/AA0026.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0026.PDB" />
-</Entry>
-<Entry id="AA0027">
-<Header>
-<Code>AA0027</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>(2S,3R)-3-hydroxyaspartic acid</Name>
-<AlternateName>2-amino-3-hydroxysuccinic acid</AlternateName>
-<AlternateName>2-azanyl-3-hydroxybutanedioic acid</AlternateName>
-<AlternateName>3-hydroxyaspartic acid</AlternateName>
-<AlternateName>L-erythro-beta-hydroxyaspartic acid</AlternateName>
-<SystematicName>(2S,3R)-2-amino-3-hydroxybutanedioic acid</SystematicName>
-<Xref>CAS:17576</Xref>
-<Xref>CAS:7298-98-8</Xref>
-<Xref>ChEBI:17576</Xref>
-<Xref>PDBHET:BH2</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 5 N 1 O 4</Formula>
-<Weight type="chemical">131.09</Weight>
-<Weight type="physical">131.021858</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0004">
-<Formula>C 0 H 0 N 0 O 1</Formula>
-<Weight type="chemical">16.00</Weight>
-<Weight type="physical">15.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kornguth, M.L.</Author>
-<Author>Sallach, H.J.</Author>
-</Authors>
-<Citation>Arch. Biochem. Biophys. 91, 39-42, 1960</Citation>
-<Title>(beta)-Hydroxyaspartic acid: synthesis and separation of its diastereoisomers.</Title>
-<Xref>PMID:13753215</Xref>
-<Note>chemical synthesis and diastereomeric separation</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Drakenberg, T.</Author>
-<Author>Fernlund, P.</Author>
-<Author>Roepstorff, P.</Author>
-<Author>Stenflo, J.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 80, 1802-1806, 1983</Citation>
-<Title>beta-Hydroxyaspartic acid in vitamin K-dependent protein C.</Title>
-<Xref>DOI:10.1073/pnas.80.7.1802</Xref>
-<Xref>PMID:6572939</Xref>
-<Note>mass spectrometric detection; the stereochemistry was determined by hydrolysis and comparison with "erythro-beta-hydroxyaspartic acid"</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>McMullen, B.A.</Author>
-<Author>Fujikawa, K.</Author>
-<Author>Kisiel, W.</Author>
-<Author>Sasagawa, T.</Author>
-<Author>Howald, W.N.</Author>
-<Author>Kwa, E.Y.</Author>
-<Author>Weinstein, B.</Author>
-</Authors>
-<Citation>Biochemistry 22, 2875-2884, 1983</Citation>
-<Title>Complete amino acid sequence of the light chain of human blood coagulation factor X: evidence for identification of residue 63 as beta-hydroxyaspartic acid.</Title>
-<Xref>DOI:10.1021/bi00281a016</Xref>
-<Xref>PMID:6871167</Xref>
-<Note>mass spectrometric and (1)H-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kessler, H.</Author>
-<Author>Steuernagel, S.</Author>
-<Author>Will, M.</Author>
-<Author>Jung, G.</Author>
-<Author>Kellner, R.</Author>
-<Author>Gillessen, D.</Author>
-<Author>Kamiyama, T.</Author>
-</Authors>
-<Citation>Helv. Chim. Acta 71, 1924-1929, 1988</Citation>
-<Title>The structure of the polycyclic nonadecapeptide Ro 09-0198.</Title>
-<Xref>DOI:10.1002/hlca.19880710811</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Padmanabhan, K.</Author>
-<Author>Padmanabhan, K.P.</Author>
-<Author>Tulinsky, A.</Author>
-<Author>Park, C.H.</Author>
-<Author>Bode, W.</Author>
-<Author>Huber, R.</Author>
-<Author>Blankenship, D.T.</Author>
-<Author>Cardin, A.D.</Author>
-<Author>Kisiel, W.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 232, 947-966, 1993</Citation>
-<Title>Structure of human des(1-45) factor Xa at 2.2 angstroms resolution.</Title>
-<Xref>DOI:10.1006/jmbi.1993.1441</Xref>
-<Xref>PMID:8355279</Xref>
-<Note>X-ray diffraction, 2.2 angstroms</Note>
-</ReferenceBlock>
-<Comment>This diastereomeric form has been found in the EGF domain of many proteins. For the (2S,3S)-diastereomer, see RESID:AA0579.</Comment>
-<Comment>The Enzyme Commission has not yet distinguished the different stereospecific enzyme activities.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptide-aspartate beta-dioxygenase (EC 1.14.11.16)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>D</SequenceSpec>
-<Xref>GO:0019715</Xref>
-<Xref>PSI-MOD:00036</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__(3r)-3-hydroxyaspartate__d">MOD_RES (3R)-3-hydroxyaspartate</Feature>
-</Features>
-<Image src="/images/AA0027.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0027.PDB" />
-</Entry>
-<Entry id="AA0028">
-<Header>
-<Code>AA0028</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-Mar-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>(2S,5R)-5-hydroxylysine</Name>
-<AlternateName>2,6-bisazanyl-5-hydroxyhexanoic acid</AlternateName>
-<AlternateName>2,6-diamino-2,3,4,6-tetradeoxyhexonic acid</AlternateName>
-<AlternateName>alpha,epsilon-diamino-delta-hydroxycaproic acid</AlternateName>
-<AlternateName>L-erythro-delta-hydroxylysine</AlternateName>
-<SystematicName>(2S,5R)-2,6-diamino-5-hydroxyhexanoic acid</SystematicName>
-<Xref>CAS:1190-94-9</Xref>
-<Xref>ChEBI:18040</Xref>
-<Xref>PDBHET:LYZ</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 12 N 2 O 2</Formula>
-<Weight type="chemical">144.17</Weight>
-<Weight type="physical">144.089878</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 0 H 0 N 0 O 1</Formula>
-<Weight type="chemical">16.00</Weight>
-<Weight type="physical">15.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bergstrom, S.</Author>
-<Author>Lindstedt, S.</Author>
-</Authors>
-<Citation>Acta Chem. Scand. 5, 157-167, 1951</Citation>
-<Title>On the isolation and structure of hydroxylysine.</Title>
-<Xref>DOI:10.3891/acta.chem.scand.05-0157</Xref>
-<Note>structure of collagen derived compound established as 5-hydroxylysine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Witkop, B.</Author>
-</Authors>
-<Citation>Experientia 12, 372-374, 1956</Citation>
-<Title>The application of Hudson's lactone rule to gamma- and delta-hydroxyamino acids and the question of the configuration of delta-hydroxy-L-lysine from collagen.</Title>
-<Xref>DOI:10.1007/BF02157272</Xref>
-<Xref>PMID:13375629</Xref>
-<Note>determination of the relative configurations for the two chiral centers of collagen derived 5-hydroxylysine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Spiess, J.</Author>
-<Author>Noe, B.D.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 82, 277-281, 1985</Citation>
-<Title>Processing of an anglerfish somatostatin precursor to a hydroxylysine-containing somatostatin 28.</Title>
-<Xref>DOI:10.1073/pnas.82.2.277</Xref>
-<Xref>PMID:2857489</Xref>
-<Note>chromatographic detection of PTH derivative</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Teshima, T.</Author>
-<Author>Ueki, Y.</Author>
-<Author>Nakai, T.</Author>
-<Author>Shiba, T.</Author>
-</Authors>
-<Citation>Tetrahedron 42, 829-834, 1986</Citation>
-<Title>Structure determination of lepidopteran, self-defense substance produced by silkworm.</Title>
-<Xref>DOI:10.1016/S0040-4020(01)87488-3</Xref>
-<Note>chromatographic detection</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Doust, A.B.</Author>
-<Author>Marai, C.N.J.</Author>
-<Author>Harrop, S.J.</Author>
-<Author>Wilk, K.E.</Author>
-<Author>Curmi, P.M.G.</Author>
-<Author>Scholes, G.D.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 344, 135-153, 2004</Citation>
-<Title>Developing a structure-function model for the cryptophyte phycoerythrin 545 using ultrahigh resolution crystallography and ultrafast laser spectroscopy.</Title>
-<Xref>DOI:10.1016/j.jmb.2004.09.044</Xref>
-<Xref>PMID:15504407</Xref>
-<Note>X-ray diffraction, 0.97 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Doust, A.B.</Author>
-<Author>Marai, C.N.J.</Author>
-<Author>Harrop, S.J.</Author>
-<Author>Wilk, K.E.</Author>
-<Author>Curmi, P.M.G.</Author>
-<Author>Scholes, G.D.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, September 2004</Citation>
-<Description>High resolution crystal structure of phycoerythrin 545 from the marine cryptophyte Rhodomonas CS24.</Description>
-<Xref>PDB:1XG0</Xref>
-<Note>X-ray diffraction, 0.97 angstroms; the stereoisomer is (2S,5R)</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Aguilar, M.B.</Author>
-<Author>Lopez-Vera, E.</Author>
-<Author>Ortiz, E.</Author>
-<Author>Becerril, B.</Author>
-<Author>Possani, L.D.</Author>
-<Author>Olivera, B.M.</Author>
-<Author>Heimer de la Cotera, E.P.</Author>
-</Authors>
-<Citation>Biochemistry 44, 11130-11136, 2005</Citation>
-<Title>A novel conotoxin from Conus delessertii with posttranslationally modified lysine residues.</Title>
-<Xref>DOI:10.1021/bi050518l</Xref>
-<Xref>PMID:16101297</Xref>
-<Note>mass spectrometric detection; chromatographic identification of the PTH derivative (2S,5R) stereoisomer</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Myllylä, R.</Author>
-<Author>Wang, C.</Author>
-<Author>Heikkinen, J.</Author>
-<Author>Juffer, A.</Author>
-<Author>Lampela, O.</Author>
-<Author>Risteli, M.</Author>
-<Author>Ruotsalainen, H.</Author>
-<Author>Salo, A.</Author>
-<Author>Sipilä, L.</Author>
-</Authors>
-<Citation>J. Cell. Physiol. 212, 323-329, 2007</Citation>
-<Title>Expanding the lysyl hydroxylase toolbox: new insights into the localization and activities of lysyl hydroxylase 3 (LH3).</Title>
-<Xref>DOI:10.1002/jcp.21036</Xref>
-<Xref>PMID:17516569</Xref>
-<Note>lysyl hydroxylase 3 (LH3) also possesses galactosyl transferase and glucosyl transferase activities</Note>
-</ReferenceBlock>
-<Comment>Some forms of lysyl hydroxylase are multifunctional and possess both galactosyltransferase (EC 2.4.1.50) and glucosyltransferase (EC 2.4.1.66) activities.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>procollagen-lysine 5-dioxygenase (EC 1.14.11.4)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Condition>incidental to RESID:AA0153</Condition>
-<Xref>GO:0018395</Xref>
-<Xref>PSI-MOD:00037</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__5-hydroxylysine__k">MOD_RES (2S,5R)-5-hydroxylysine</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="mod_res__5-hydroxylysine__k">MOD_RES 5-hydroxylysine</Feature>
-<Note>this UniProt feature is used when the stereochemistry has not been determined</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0028.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0028.PDB" />
-</Entry>
-<Entry id="AA0029">
-<Header>
-<Code>AA0029</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>3-hydroxy-L-proline</Name>
-<AlternateName>3-trans-hydroxy-L-proline</AlternateName>
-<AlternateName>beta-hydroxypyrrolidine-alpha-carboxylic acid</AlternateName>
-<AlternateName>L-threo-3-hydroxyproline</AlternateName>
-<SystematicName>(2S,3S)-3-hydroxypyrrolidine-2-carboxylic acid</SystematicName>
-<Xref>CAS:4298-08-2</Xref>
-<Xref>ChEBI:85428</Xref>
-<Xref>PDBHET:HY3</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 7 N 1 O 2</Formula>
-<Weight type="chemical">113.12</Weight>
-<Weight type="physical">113.047678</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0015">
-<Formula>C 0 H 0 N 0 O 1</Formula>
-<Weight type="chemical">16.00</Weight>
-<Weight type="physical">15.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ogle, J.D.</Author>
-<Author>Arlinghaus, R.B.</Author>
-<Author>Logan, M.A.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 237, 3667-3673, 1962</Citation>
-<Title>3-Hydroxyproline, a new amino acid of collagen.</Title>
-<Xref>PMID:13939597</Xref>
-<Note>mass spectrometric and chemical characterization; the spelling of Logan in the PubMed citation is corrected</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fietzek, P.P.</Author>
-<Author>Rexrodt, F.W.</Author>
-<Author>Wendt, P.</Author>
-<Author>Stark, M.</Author>
-<Author>Kuehn, K.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 30, 163-168, 1972</Citation>
-<Title>The covalent structure of collagen. Amino acid sequence of peptide alpha1-CB6-C2.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1972.tb02083.x</Xref>
-<Xref>PMID:4343807</Xref>
-<Note>chromatographic detection</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Waite, J.H.</Author>
-</Authors>
-<Citation>J. Comp. Physiol. B, Biochem. Syst. Environ. Physiol. 156, 491-496, 1986</Citation>
-<Title>Mussel glue from Mytilus californianus Conrad: a comparative study.</Title>
-<Xref>DOI:10.1007/BF00691034</Xref>
-<Xref>PMID:3734192</Xref>
-<Note>chromatographic detection</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kassel, D.B.</Author>
-<Author>Biemann, K.</Author>
-</Authors>
-<Citation>Anal. Chem. 62, 1691-1695, 1990</Citation>
-<Title>Differentiation of hydroxyproline isomers and isobars in peptides by tandem mass spectrometry.</Title>
-<Xref>DOI:10.1021/ac00214a032</Xref>
-<Xref>PMID:2400108</Xref>
-<Note>attempts to distinguish from isobaric 4-hydroxyproline (see RESID:AA0030) with tandem mass spectrometry</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Eyre, D.R.</Author>
-<Author>Weis, M.</Author>
-<Author>Hudson, D.M.</Author>
-<Author>Wu, J.J.</Author>
-<Author>Kim, L.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 286, 7732-7736, 2011</Citation>
-<Title>A novel 3-hydroxyproline (3Hyp)-rich motif marks the triple-helical C terminus of tendon type I collagen.</Title>
-<Xref>DOI:10.1074/jbc.C110.195768</Xref>
-<Xref>PMID:21239503</Xref>
-<Note>mass spectrometric and chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Loenarz, C.</Author>
-<Author>Sekirnik, R.</Author>
-<Author>Thalhammer, A.</Author>
-<Author>Ge, W.</Author>
-<Author>Spivakovsky, E.</Author>
-<Author>Mackeen, M.M.</Author>
-<Author>McDonough, M.A.</Author>
-<Author>Cockman, M.E.</Author>
-<Author>Kessler, B.M.</Author>
-<Author>Ratcliffe, P.J.</Author>
-<Author>Wolf, A.</Author>
-<Author>Schofield, C.J.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 111, 4019-4024, 2014</Citation>
-<Title>Hydroxylation of the eukaryotic ribosomal decoding center affects termination efficiency.</Title>
-<Xref>DOI:10.1073/pnas.1311750111</Xref>
-<Xref>PMID:24550462</Xref>
-<Note>modification of Saccharomyces cerevisiae ribosomal protein S23 proline-64 to trans-3-hydroxyproline improves translation accuracy</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Katz, M.J.</Author>
-<Author>Acevedo, J.M.</Author>
-<Author>Loenarz, C.</Author>
-<Author>Galagovsky, D.</Author>
-<Author>Liu-Yi, P.</Author>
-<Author>Pérez-Pepe, M.</Author>
-<Author>Thalhammer, A.</Author>
-<Author>Sekirnik, R.</Author>
-<Author>Ge, W.</Author>
-<Author>Melani, M.</Author>
-<Author>Thomas, M.G.</Author>
-<Author>Simonetta, S.</Author>
-<Author>Boccaccio, G.L.</Author>
-<Author>Schofield, C.J.</Author>
-<Author>Cockman, M.E.</Author>
-<Author>Ratcliffe, P.J.</Author>
-<Author>Wappner, P.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 111, 4025-4030, 2014</Citation>
-<Title>Sudestada1, a Drosophila ribosomal prolyl-hydroxylase required for mRNA translation, cell homeostasis, and organ growth.</Title>
-<Xref>DOI:10.1073/pnas.1314485111</Xref>
-<Xref>PMID:24550463</Xref>
-<Note>modification of Drosophila melanogaster ribosomal protein S23 proline-62 to hydroxyproline; the regioisomer and the stereoisomer were not determined</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Singleton, R.S.</Author>
-<Author>Liu-Yi, P.</Author>
-<Author>Formenti, F.</Author>
-<Author>Ge, W.</Author>
-<Author>Sekirnik, R.</Author>
-<Author>Fischer, R.</Author>
-<Author>Adam, J.</Author>
-<Author>Pollard, P.J.</Author>
-<Author>Wolf, A.</Author>
-<Author>Thalhammer, A.</Author>
-<Author>Loenarz, C.</Author>
-<Author>Flashman, E.</Author>
-<Author>Yamamoto, A.</Author>
-<Author>Coleman, M.L.</Author>
-<Author>Kessler, B.M.</Author>
-<Author>Wappner, P.</Author>
-<Author>Schofield, C.J.</Author>
-<Author>Ratcliffe, P.J.</Author>
-<Author>Cockman, M.E.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 111, 4031-4036, 2014</Citation>
-<Title>OGFOD1 catalyzes prolyl hydroxylation of RPS23 and is involved in translation control and stress granule formation.</Title>
-<Xref>DOI:10.1073/pnas.1314482111</Xref>
-<Xref>PMID:24550447</Xref>
-<Note>modification of human ribosomal protein S23 proline-62 to hydroxyproline; the regioisomer and the stereoisomer were not determined</Note>
-</ReferenceBlock>
-<Comment>There are at least three different genes for procollagen-proline 3-dioxygenase in mammals with different specificities and patterns of tissue expression. Usually proline 3-hydroxylation occurs at the second position of specific GPP sequences in collagen chains and is preceded by proline 4-hydroxylation of the proline in the third position. See RESID:AA0030.</Comment>
-<Comment>Eukaryotic ribosomal protein S23 can be hydroxylated at a specific proline and the modification affects translation accuracy and termination efficiency.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>procollagen-proline 3-dioxygenase (EC 1.14.11.7)</EnzymeName>
-<EnzymeName>[ribosomal protein S23]-proline 3-dioxygenase, OGFOD1, Sudestada1, Tpa1p, (EC 1.14.11.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>P</SequenceSpec>
-<Condition>incidental to RESID:AA0030</Condition>
-<Xref>GO:0018400</Xref>
-<Xref>PSI-MOD:00038</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__3-hydroxyproline__p">MOD_RES 3-hydroxyproline</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="mod_res__hydroxyproline__p">MOD_RES Hydroxyproline</Feature>
-<Note>this UniProt feature is used when the isomeric structure has not been determined</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0029.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0029.PDB" />
-</Entry>
-<Entry id="AA0030">
-<Header>
-<Code>AA0030</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>4-hydroxy-L-proline</Name>
-<AlternateName>4-hydroxyproline</AlternateName>
-<AlternateName>4-trans-hydroxy-L-proline</AlternateName>
-<AlternateName>gamma-hydroxypyrrolidine-alpha-carboxylic acid</AlternateName>
-<AlternateName>L-threo-4-hydroxyproline</AlternateName>
-<SystematicName>(2S,4R)-4-hydroxypyrrolidine-2-carboxylic acid</SystematicName>
-<Xref>CAS:51-35-4</Xref>
-<Xref>ChEBI:61965</Xref>
-<Xref>PDBHET:HYP</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 7 N 1 O 2</Formula>
-<Weight type="chemical">113.12</Weight>
-<Weight type="physical">113.047678</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0015">
-<Formula>C 0 H 0 N 0 O 1</Formula>
-<Weight type="chemical">16.00</Weight>
-<Weight type="physical">15.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Waite, J.H.</Author>
-</Authors>
-<Citation>J. Comp. Physiol. B, Biochem. Syst. Environ. Physiol. 156, 491-496, 1986</Citation>
-<Title>Mussel glue from Mytilus californianus Conrad: a comparative study.</Title>
-<Xref>DOI:10.1007/BF00691034</Xref>
-<Xref>PMID:3734192</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kassel, D.B.</Author>
-<Author>Biemann, K.</Author>
-</Authors>
-<Citation>Anal. Chem. 62, 1691-1695, 1990</Citation>
-<Title>Differentiation of hydroxyproline isomers and isobars in peptides by tandem mass spectrometry.</Title>
-<Xref>DOI:10.1021/ac00214a032</Xref>
-<Xref>PMID:2400108</Xref>
-<Note>attempts to distinguish from isobaric 3-hydroxyproline (see RESID:AA0029) with tandem mass spectrometry</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Jaakkola, P.</Author>
-<Author>Mole, D.R.</Author>
-<Author>Tian, Y.M.</Author>
-<Author>Wilson, M.I.</Author>
-<Author>Gielbert, J.</Author>
-<Author>Gaskell, S.J.</Author>
-<Author>von Kriegsheim, A.</Author>
-<Author>Hebestreit, H.F.</Author>
-<Author>Mukherji, M.</Author>
-<Author>Schofield, C.J.</Author>
-<Author>Maxwell, P.H.</Author>
-<Author>Pugh, C.W.</Author>
-<Author>Ratcliffe, P.J.</Author>
-</Authors>
-<Citation>Science 292, 468-472, 2001</Citation>
-<Title>Targeting of HIF-alpha to the von Hippel-Lindau ubiquitylation complex by O2-regulated prolyl hydroxylation.</Title>
-<Xref>DOI:10.1126/science.1059796</Xref>
-<Xref>PMID:11292861</Xref>
-<Note>mass spectrometric detection; the stereochemistry was not determined; in this protein this is a regulatory modification, apparently competitive with hydoxylation of an asparagine in another domain (see RESID:AA0026)</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Min, J.H.</Author>
-<Author>Yang, H.</Author>
-<Author>Ivan, M.</Author>
-<Author>Gertler, F.</Author>
-<Author>Kaelin Jr., W.G.</Author>
-<Author>Pavletich, N.P.</Author>
-</Authors>
-<Citation>Science 296, 1886-1889, 2002</Citation>
-<Title>Structure of an HIF-1alpha-pVHL complex: hydroxyproline recognition in signaling.</Title>
-<Xref>DOI:10.1126/science.1073440</Xref>
-<Xref>PMID:12004076</Xref>
-<Note>X-ray diffraction, 1.85 angstroms; the bound peptide containing (2S,4R)-4-hydroxyproline is synthetic</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Min, J.-H.</Author>
-<Author>Yang, H.</Author>
-<Author>Ivan, M.</Author>
-<Author>Gertler, F.</Author>
-<Author>Kaelin, W. G. Jr.</Author>
-<Author>Pavletich, N.P.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, April 2002</Citation>
-<Description>Structure of a HIF-1A-PVHL-ElonginB-ElonginC Complex.</Description>
-<Xref>PDB:1LM8</Xref>
-<Note>X-ray diffraction, 1.85 angstroms</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>procollagen-proline 4-dioxygenase (EC 1.14.11.2)</EnzymeName>
-<EnzymeName>hypoxia-inducible factor-proline dioxygenase (EC 1.14.11.29)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>P</SequenceSpec>
-<Xref>GO:0018401</Xref>
-<Xref>PSI-MOD:00039</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__4-hydroxyproline__p">MOD_RES 4-hydroxyproline</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="mod_res__hydroxyproline__p">MOD_RES Hydroxyproline</Feature>
-<Note>this UniProt feature is used when the isomeric structure has not been determined</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0030.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0030.PDB" />
-</Entry>
-<Entry id="AA0031">
-<Header>
-<Code>AA0031</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Sep-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>2-pyrrolidone-5-carboxylic acid</Name>
-<AlternateName>2-oxopyrrolidine-5-carboxylic acid</AlternateName>
-<AlternateName>5-oxoproline</AlternateName>
-<AlternateName>5-oxopyrrolidine-2-carboxylic acid</AlternateName>
-<AlternateName>5-pyrrolidone-2-carboxylic acid</AlternateName>
-<AlternateName>PCA</AlternateName>
-<AlternateName>pyroglutamic acid</AlternateName>
-<SystematicName>(2S)-5-oxo-2-pyrrolidinecarboxylic acid</SystematicName>
-<Xref>CAS:98-79-3</Xref>
-<Xref>ChEBI:30652</Xref>
-<Xref>PDBHET:PCA</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 6 N 1 O 2</Formula>
-<Weight type="chemical">112.11</Weight>
-<Weight type="physical">112.039853</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0006" label="GLU">
-<Formula>C 0 H -2 N 0 O -1</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0007" label="GLN">
-<Formula>C 0 H -3 N -1 O 0</Formula>
-<Weight type="chemical">-17.03</Weight>
-<Weight type="physical">-17.026549</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sanger, F.</Author>
-<Author>Thompson, E.O.</Author>
-<Author>Kitai, R.</Author>
-</Authors>
-<Citation>Biochem. J. 59, 509-518, 1955</Citation>
-<Title>The amide groups of insulin.</Title>
-<Xref>PMID:14363129</Xref>
-<Note>observes that an N-terminal glutaminyl residue tends to cyclize to a pyrrolidone carboxylic acid under acid conditions</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Podell, D.N.</Author>
-<Author>Abraham, G.N.</Author>
-</Authors>
-<Citation>Biochem. Biophys. Res. Commun. 81, 176-185, 1978</Citation>
-<Title>A technique for the removal of pyroglutamic acid from the amino terminus of proteins using calf liver pyroglutamate amino peptidase.</Title>
-<Xref>DOI:10.1016/0006-291X(78)91646-7</Xref>
-<Xref>PMID:26343</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fischer, W.H.</Author>
-<Author>Spiess, J.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 84, 3628-3632, 1987</Citation>
-<Title>Identification of a mammalian glutaminyl cyclase converting glutaminyl into pyroglutamyl peptides.</Title>
-<Xref>DOI:10.1073/pnas.84.11.3628</Xref>
-<Xref>PMID:3473473</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Betancourt, L.</Author>
-<Author>Takao, T.</Author>
-<Author>Hernandez, L.</Author>
-<Author>Padron, G.</Author>
-<Author>Shimonishi, Y.</Author>
-</Authors>
-<Citation>J. Mass Spectrom. 34, 169-174, 1999</Citation>
-<Title>Structural characterization of Acetobacter diazotropicus levansucrase by matrix-assisted laser desorption/ionization mass spectrometry: identification of an N-terminal blocking group and a free-thiol cysteine residue.</Title>
-<Xref>DOI:10.1002/(SICI)1096-9888(199903)34:3&lt;169::AID-JMS780&gt;3.0.CO;2-4</Xref>
-<Xref>PMID:10214721</Xref>
-<Note>mass spectrometric detection</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Garden, R.W.</Author>
-<Author>Moroz, T.P.</Author>
-<Author>Gleeson, J.M.</Author>
-<Author>Floyd, P.D.</Author>
-<Author>Li, L.</Author>
-<Author>Rubakhin, S.S.</Author>
-<Author>Sweedler, J.V.</Author>
-</Authors>
-<Citation>J. Neurochem. 72, 676-681, 1999</Citation>
-<Title>Formation of N-pyroglutamyl peptides from N-Glu and N-Gln precursors in Aplysia neurons.</Title>
-<Xref>PMID:9930740</Xref>
-<Note>mass spectrometric detection; the source was peptide in single neuron cells; partial conversion of N-terminal glutamate was observed and appeared to be dependent on a temperature sensitive factor</Note>
-</ReferenceBlock>
-<Comment>This modification can form artifactually from amino-terminal glutamine under mildly acid conditions, and from amino-terminal glutamic acid under very acid or anhydrous conditions.</Comment>
-<Comment>The presumed enzyme in Aplysia neurons has not been characterized. The reaction probably requires concomitant hydrolysis of a compound such as ATP.</Comment>
-<GeneratingEnzyme>
-<EnzymeName link="GLN">glutaminyl-peptide cyclotransferase (EC 2.3.2.5)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode link="GLN">
-<SequenceSpec>Q</SequenceSpec>
-<Abbreviation>Glp</Abbreviation>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0017186</Xref>
-<Xref>PSI-MOD:00040</Xref>
-</SequenceCode>
-<SequenceCode link="GLU">
-<SequenceSpec>E</SequenceSpec>
-<Abbreviation>Glp</Abbreviation>
-<Condition>amino-terminal</Condition>
-<Xref>PSI-MOD:00420</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-<Keyword>pyroglutamic acid</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__pyrrolidone carboxylic acid__q" link="GLN">MOD_RES Pyrrolidone carboxylic acid</Feature>
-<Feature type="UniProt" key="mod_res__pyrrolidone carboxylic acid ?glu?__e" link="GLU">MOD_RES Pyrrolidone carboxylic acid (Glu)</Feature>
-</Features>
-<Image src="/images/AA0031.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0031.PDB" />
-</Entry>
-<Entry id="AA0032">
-<Header>
-<Code>AA0032</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-gamma-carboxyglutamic acid</Name>
-<AlternateName>(3S)-3-azanylpropane-1,1,3-tricarboxylic acid</AlternateName>
-<AlternateName>1-carboxyglutamic acid [misnomer]</AlternateName>
-<AlternateName>3-amino-1,1,3-propanetricarboxylic acid</AlternateName>
-<AlternateName>3-azanylpropane-1,1,3-tricarboxylic acid</AlternateName>
-<AlternateName>4-carboxyglutamic acid</AlternateName>
-<SystematicName>(3S)-3-aminopropane-1,1,3-tricarboxylic acid</SystematicName>
-<Xref>CAS:53861-57-7</Xref>
-<Xref>ChEBI:61939</Xref>
-<Xref>PDBHET:CGU</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 7 N 1 O 5</Formula>
-<Weight type="chemical">173.12</Weight>
-<Weight type="physical">173.032422</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0006">
-<Formula>C 1 H 0 N 0 O 2</Formula>
-<Weight type="chemical">44.01</Weight>
-<Weight type="physical">43.989829</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Stenflo, J.</Author>
-<Author>Fernlund, P.</Author>
-<Author>Egan, W.</Author>
-<Author>Roepstorff, P.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 71, 2730-2733, 1974</Citation>
-<Title>Vitamin K dependent modifications of glutamic acid residues in prothrombin.</Title>
-<Xref>DOI:10.1073/pnas.71.7.2730</Xref>
-<Xref>PMID:4528109</Xref>
-<Note>mass spectrometric and (1)H-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hauschka, P.V.</Author>
-<Author>Henson, E.B.</Author>
-<Author>Gallop, P.M.</Author>
-</Authors>
-<Citation>Anal. Biochem. 108, 57-63, 1980</Citation>
-<Title>Quantitative analysis and comparative decarboxylation of aminomalonic acid, beta-carboxyaspartic acid, and gamma-carboxyglutamic acid.</Title>
-<Xref>DOI:10.1016/0003-2697(80)90691-0</Xref>
-<Xref>PMID:7457858</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Smalley, D.M.</Author>
-<Author>Preusch, P.C.</Author>
-</Authors>
-<Citation>Anal. Biochem. 172, 241-247, 1988</Citation>
-<Title>Analysis of gamma-carboxyglutamic acid by reverse phase HPLC of its phenylthiocarbamyl derivative.</Title>
-<Xref>DOI:10.1016/0003-2697(88)90438-1</Xref>
-<Xref>PMID:3263814</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Cairns, J.R.</Author>
-<Author>Williamson, M.K.</Author>
-<Author>Price, P.A.</Author>
-</Authors>
-<Citation>Anal. Biochem. 199, 93-97, 1991</Citation>
-<Title>Direct identification of gamma-carboxyglutamic acid in the sequencing of vitamin K-dependent proteins.</Title>
-<Xref>DOI:10.1016/0003-2697(91)90274-W</Xref>
-<Xref>PMID:1807167</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Nishimoto, S.K.</Author>
-<Author>Zhao, J.</Author>
-<Author>Dass, C.</Author>
-</Authors>
-<Citation>Anal. Biochem. 216, 159-164, 1994</Citation>
-<Title>Isolation and characterization of the reaction product of 4-diazobenzenesulfonic acid and gamma-carboxyglutamic acid: modification of the assay for measurement of beta-carboxyaspartic acid.</Title>
-<Xref>DOI:10.1006/abio.1994.1020</Xref>
-<Xref>PMID:8135347</Xref>
-<Note>colorimetric detection</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Morris, D.P.</Author>
-<Author>Stevens, R.D.</Author>
-<Author>Wright, D.J.</Author>
-<Author>Stafford, D.W.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 270, 30491-30498, 1995</Citation>
-<Title>Processive post-translational modification. Vitamin K-dependent carboxylation of a peptide substrate.</Title>
-<Xref>PMID:8530480</Xref>
-<Note>processing mechanism of vitamin K-dependent gamma-glutamyl carboxylase</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Nakamura, T.</Author>
-<Author>Yu, Z.</Author>
-<Author>Fainzilber, M.</Author>
-<Author>Burlingame, A.L.</Author>
-</Authors>
-<Citation>Protein Sci. 5, 524-530, 1996</Citation>
-<Title>Mass spectrometric-based revision of the structure of a cysteine-rich peptide toxin with gamma-carboxyglutamic acid, TxVIIA, from the sea snail, Conus textile.</Title>
-<Xref>DOI:10.1002/pro.5560050315</Xref>
-<Xref>PMID:8868490</Xref>
-<Note>mass spectrometric identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Rigby, A.C.</Author>
-<Author>Baleja, J.D.</Author>
-<Author>Furie, B.C.</Author>
-<Author>Furie, B.</Author>
-</Authors>
-<Citation>Biochemistry 36, 6906-6914, 1997</Citation>
-<Title>Three-dimensional structure of a gamma-carboxyglutamic acid-containing conotoxin, conantokin G, from the marine snail Conus geographus: the metal-free conformer.</Title>
-<Xref>DOI:10.1021/bi970321w</Xref>
-<Xref>PMID:9188685</Xref>
-<Note>characterization and conformation by (1)H-NMR</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kelleher, N.L.</Author>
-<Author>Zubarev, R.A.</Author>
-<Author>Bush, K.</Author>
-<Author>Furie, B.</Author>
-<Author>Furie, B.C.</Author>
-<Author>McLafferty, F.W.</Author>
-<Author>Walsh, C.T.</Author>
-</Authors>
-<Citation>Anal. Chem. 71, 4250-4253, 1999</Citation>
-<Title>Localization of labile posttranslational modifications by electron capture dissociation: the case of gamma-carboxyglutamic acid.</Title>
-<Xref>DOI:10.1021/ac990684x</Xref>
-<Xref>PMID:10517147</Xref>
-<Note>detection in tandem mass spectrometry by electron capture dissociation</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bandyopadhyay, P.K.</Author>
-<Author>Garrett, J.E.</Author>
-<Author>Shetty, R.P.</Author>
-<Author>Keate, T.</Author>
-<Author>Walker, C.S.</Author>
-<Author>Olivera, B.M.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 99, 1264-1269, 2002</Citation>
-<Title>γ-Glutamyl carboxylation: An extracellular posttranslational modification that antedates the divergence of molluscs, arthropods, and chordates.</Title>
-<Xref>DOI:10.1073/pnas.022637099</Xref>
-<Xref>PMID:11818531</Xref>
-<Note>evolutionary considerations</Note>
-</ReferenceBlock>
-<Comment>The gamma-carboxylation of glutamic acid residues is performed by a vitamin K-dependent enzyme.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptidyl-glutamate 4-carboxylase</EnzymeName>
-<EnzymeName>peptidyl-glutamate 4-carboxylase (2-methyl-3-phytyl-1,4-naphthoquinol-epoxidizing) (EC 4.1.1.90)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>E</SequenceSpec>
-<Abbreviation>Gla</Abbreviation>
-<Xref>GO:0017187</Xref>
-<Xref>PSI-MOD:00041</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>carboxyglutamic acid</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__4-carboxyglutamate__e">MOD_RES 4-carboxyglutamate</Feature>
-</Features>
-<Image src="/images/AA0032.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0032.PDB" />
-</Entry>
-<Entry id="AA0033">
-<Header>
-<Code>AA0033</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-aspartic 4-phosphoric anhydride</Name>
-<AlternateName>2-aminobutanedioic 4-phosphoric anhydride</AlternateName>
-<AlternateName>2-azanyl-4-oxo-4-(phosphonooxy)butanoic acid</AlternateName>
-<AlternateName>4-oxo-O-phosphono-L-homoserine</AlternateName>
-<AlternateName>4-phosphoaspartic acid</AlternateName>
-<AlternateName>beta-aspartyl phosphate</AlternateName>
-<SystematicName>(2S)-2-amino-4-oxo-4-(phosphonooxy)butanoic acid</SystematicName>
-<Xref>CAS:22138-53-0</Xref>
-<Xref>ChEBI:137319</Xref>
-<Xref>ChEBI:15836</Xref>
-<Xref>PDBHET:PHD</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 6 N 1 O 6 P 1</Formula>
-<Weight type="chemical">195.07</Weight>
-<Weight type="physical">194.993274</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0004">
-<Formula>C 0 H 1 N 0 O 3 P 1</Formula>
-<Weight type="chemical">79.98</Weight>
-<Weight type="physical">79.966331</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bastide, F.</Author>
-<Author>Meissner, G.</Author>
-<Author>Fleischer, S.</Author>
-<Author>Post, R.L.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 248, 8385-8391, 1973</Citation>
-<Title>Similarity of the active site of phosphorylation of the adenosine triphosphatase for transport of sodium and potassium ions in kidney to that for transport of calcium ions in the sarcoplasmic reticulum of muscle.</Title>
-<Xref>PMID:4357737</Xref>
-<Note>chromatographic detection; chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Collet, J.F.</Author>
-<Author>Stroobant, V.</Author>
-<Author>Pirard, M.</Author>
-<Author>Delpierre, G.</Author>
-<Author>Van Schaftingen, E.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 273, 14107-14112, 1998</Citation>
-<Title>A new class of phosphotransferases phosphorylated on an aspartate residue in an amino-terminal DXDX(T/V) motif.</Title>
-<Xref>PMID:9603909</Xref>
-<Note>chemical detection using sodium borohydride</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>D</SequenceSpec>
-<Xref>GO:0018443</Xref>
-<Xref>PSI-MOD:00042</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="act_site__4-aspartylphosphate intermediate__d">ACT_SITE 4-aspartylphosphate intermediate</Feature>
-<Feature type="UniProt" key="mod_res__4-aspartylphosphate__d">MOD_RES 4-aspartylphosphate</Feature>
-</Features>
-<Image src="/images/AA0033.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0033.PDB" />
-</Entry>
-<Entry id="AA0034">
-<Header>
-<Code>AA0034</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-Dec-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-phospho-L-cysteine</Name>
-<AlternateName>2-azanyl-3-(phosphonosulfanyl)propanoic acid</AlternateName>
-<AlternateName>cysteine phosphate thioester</AlternateName>
-<AlternateName>S-phosphonocysteine</AlternateName>
-<AlternateName>S3-phosphocysteine</AlternateName>
-<SystematicName>(2R)-2-amino-3-(phosphonosulfanyl)propanoic acid</SystematicName>
-<Xref>CAS:115562-30-6</Xref>
-<Xref>ChEBI:61956</Xref>
-<Xref>PDBHET:CSP</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 6 N 1 O 4 P 1 S 1</Formula>
-<Weight type="chemical">183.12</Weight>
-<Weight type="physical">182.975515</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 0 H 1 N 0 O 3 P 1 S 0</Formula>
-<Weight type="chemical">79.98</Weight>
-<Weight type="physical">79.966331</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Pas, H.H.</Author>
-<Author>Robillard, G.T.</Author>
-</Authors>
-<Citation>Biochemistry 27, 5835-5839, 1988</Citation>
-<Title>S-Phosphocysteine and phosphohistidine are intermediates in the phosphoenolpyruvate-dependent mannitol transport catalyzed by Escherichia coli EII(Mtl).</Title>
-<Xref>DOI:10.1021/bi00416a002</Xref>
-<Xref>PMID:3142516</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Barford, D.</Author>
-<Author>Flint, A.J.</Author>
-<Author>Tonks, N.K.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, September 1994</Citation>
-<Description>Crystal structure of human protein tyrosine phosphatase 1B.</Description>
-<Xref>PDB:2HNP</Xref>
-<Note>X-ray diffraction, 2.8 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Barford, D.</Author>
-<Author>Flint, A.J.</Author>
-<Author>Tonks, N.K.</Author>
-</Authors>
-<Citation>Science 263, 1397-1404, 1994</Citation>
-<Title>Crystal structure of human protein tyrosine phosphatase 1B.</Title>
-<Xref>DOI:10.1126/science.8128219</Xref>
-<Xref>PMID:8128219</Xref>
-<Note>X-ray diffraction, 2.8 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Zhou, G.</Author>
-<Author>Denu, J.M.</Author>
-<Author>Wu, L.</Author>
-<Author>Dixon, J.E.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 269, 28084-28090, 1994</Citation>
-<Title>The catalytic role of Cys(124) in the dual specificity phosphatase VHR.</Title>
-<Xref>PMID:7961745</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sun, F.</Author>
-<Author>Ding, Y.</Author>
-<Author>Ji, Q.</Author>
-<Author>Liang, Z.</Author>
-<Author>Deng, X.</Author>
-<Author>Wong, C.C.</Author>
-<Author>Yi, C.</Author>
-<Author>Zhang, L.</Author>
-<Author>Xie, S.</Author>
-<Author>Alvarez, S.</Author>
-<Author>Hicks, L.M.</Author>
-<Author>Luo, C.</Author>
-<Author>Jiang, H.</Author>
-<Author>Lan, L.</Author>
-<Author>He, C.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 109, 15461-15466, 2012</Citation>
-<Title>Protein cysteine phosphorylation of SarA/MgrA family transcriptional regulators mediates bacterial virulence and antibiotic resistance.</Title>
-<Xref>DOI:10.1073/pnas.1205952109</Xref>
-<Xref>PMID:22927394</Xref>
-<Note>evidence for a catalytically produced, regulatory S-phosphocysteine</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>GO:0018218</Xref>
-<Xref>GO:0018325</Xref>
-<Xref>PSI-MOD:00043</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="act_site__phosphocysteine intermediate__c">ACT_SITE Phosphocysteine intermediate</Feature>
-<Feature type="UniProt" key="mod_res__phosphocysteine__c">MOD_RES Phosphocysteine</Feature>
-</Features>
-<Image src="/images/AA0034.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0034.PDB" />
-</Entry>
-<Entry id="AA0035">
-<Header>
-<Code>AA0035</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>04-May-2001</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>1'-phospho-L-histidine</Name>
-<AlternateName>2-azanyl-3-(1-phosphono-1H-imidazol-4-yl)propanoic acid</AlternateName>
-<AlternateName>histidine-3-phosphate [misnomer]</AlternateName>
-<AlternateName>histidine-N(epsilon)-phosphate</AlternateName>
-<AlternateName>histidine-N1'-phosphate</AlternateName>
-<AlternateName>N(tau)-phosphohistidine</AlternateName>
-<AlternateName>N1-phosphonohistidine</AlternateName>
-<AlternateName>NE2-phosphonohistidine</AlternateName>
-<AlternateName>tele-phosphohistidine</AlternateName>
-<SystematicName>(2S)-2-amino-3-(1-phosphono-1H-imidazol-4-yl)propanoic acid</SystematicName>
-<Xref>CAS:5789-14-0</Xref>
-<Xref>ChEBI:83585</Xref>
-<Xref>PDBHET:NEP</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 8 N 3 O 4 P 1</Formula>
-<Weight type="chemical">217.12</Weight>
-<Weight type="physical">217.025242</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0009">
-<Formula>C 0 H 1 N 0 O 3 P 1</Formula>
-<Weight type="chemical">79.98</Weight>
-<Weight type="physical">79.966331</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hultquist, D.E.</Author>
-<Author>Moyer, R.W.</Author>
-<Author>Boyer, P.D.</Author>
-</Authors>
-<Citation>Biochemistry 5, 322-331, 1966</Citation>
-<Title>The preparation and characterization of 1-phosphohistidine and 3-phosphohistidine.</Title>
-<Xref>DOI:10.1021/bi00865a041</Xref>
-<Xref>PMID:5938947</Xref>
-<Note>the diagram page 330 indicates that what the authors call "3-phosphohistidine" corresponds to tele-phosphohistidine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hultquist, D.E.</Author>
-</Authors>
-<Citation>Biochim. Biophys. Acta 153, 329-340, 1968</Citation>
-<Title>The preparation and characterization of phosphorylated derivatives of histidine.</Title>
-<Xref>DOI:10.1016/0005-2728(68)90078-9</Xref>
-<Xref>PMID:5642389</Xref>
-<Note>chemical synthesis; chemical characterization; spectrographic characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Anonymous />
-<Group>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN)</Group>
-</Authors>
-<Citation>Eur. J. Biochem. 138, 9-37, 1984</Citation>
-<Title>Nomenclature and symbolism for amino acids and peptides. Recommendations 1983.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1984.tb07877.x</Xref>
-<Xref>PMID:6692818</Xref>
-<Note>tele-, tau-, and pros-, pi-, nomenclature</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bond, C.S.</Author>
-<Author>White, M.F.</Author>
-<Author>Hunter, W.N.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 276, 3247-3253, 2001</Citation>
-<Title>High resolution structure of the phosphohistidine-activated form of Escherichia coli cofactor-dependent phosphoglycerate mutase.</Title>
-<Xref>DOI:10.1074/jbc.M007318200</Xref>
-<Xref>PMID:11038361</Xref>
-<Note>X-ray diffraction, 1.25 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bond, C.S.</Author>
-<Author>Hunter, W.N.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, July 2000</Citation>
-<Description>E. coli cofactor-dependent phosphoglycerate mutase.</Description>
-<Xref>PDB:1E58</Xref>
-<Note>X-ray diffraction, 1.25 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Khan, S.R.</Author>
-<Author>Deutscher, J.</Author>
-<Author>Vishwakarma, R.A.</Author>
-<Author>Monedero, V.</Author>
-<Author>Bhatnagar, N.B.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 268, 521-530, 2001</Citation>
-<Title>The ptsH gene from Bacillus thuringiensis israelensis. Characterization of a new phosphorylation site on the protein HPr.</Title>
-<Xref>DOI:10.1046/j.1432-1327.2001.01878</Xref>
-<Xref>PMID:11168390</Xref>
-<Note>alternate tele-phosphorylation of a histidine, normally pros-phosphorylated, inactivates an enzyme; methods for distinguishing the isomers</Note>
-</ReferenceBlock>
-<Comment>In the older biochemical literature this is usually called histidine-3-phosphate. See also RESID:AA0036.</Comment>
-<Comment>The crystallographic designation for the substituted nitrogen is epsilon-2, E2.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>protein-histidine tele-kinase (EC 2.7.3.12)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>H</SequenceSpec>
-<Xref>GO:0018106</Xref>
-<Xref>GO:0018327</Xref>
-<Xref>PSI-MOD:00044</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>phosphohistidine</Keyword>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="act_site__tele-phosphohistidine intermediate__h">ACT_SITE Tele-phosphohistidine intermediate</Feature>
-<Feature type="UniProt" key="mod_res__tele-phosphohistidine__h">MOD_RES Tele-phosphohistidine</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="act_site__phosphohistidine intermediate__h">ACT_SITE Phosphohistidine intermediate</Feature>
-<Note>this UniProt feature is used when the isomeric structure has not been determined</Note>
-</FeatureNote>
-<FeatureNote>
-<Feature type="UniProt" key="mod_res__phosphohistidine__h">MOD_RES Phosphohistidine</Feature>
-<Note>this UniProt feature is used when the isomeric structure has not been determined</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0035.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0035.PDB" />
-</Entry>
-<Entry id="AA0036">
-<Header>
-<Code>AA0036</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>04-May-2001</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>3'-phospho-L-histidine</Name>
-<AlternateName>2-azanyl-3-(3-phosphono-3H-imidazol-4-yl)propanoic acid</AlternateName>
-<AlternateName>histidine-1-phosphate [misnomer]</AlternateName>
-<AlternateName>histidine-N(delta)-phosphate</AlternateName>
-<AlternateName>histidine-N3'-phosphate</AlternateName>
-<AlternateName>N(pi)-phosphohistidine</AlternateName>
-<AlternateName>N3-phosphonohistidine</AlternateName>
-<AlternateName>ND1-phosphonohistidine</AlternateName>
-<AlternateName>pros-phosphohistidine</AlternateName>
-<SystematicName>(2S)-2-amino-3-(3-phosphono-3H-imidazol-4-yl)propanoic acid</SystematicName>
-<Xref>CAS:5789-15-1</Xref>
-<Xref>ChEBI:64936</Xref>
-<Xref>PDBHET:HIP</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 8 N 3 O 4 P 1</Formula>
-<Weight type="chemical">217.12</Weight>
-<Weight type="physical">217.025242</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0009">
-<Formula>C 0 H 1 N 0 O 3 P 1</Formula>
-<Weight type="chemical">79.98</Weight>
-<Weight type="physical">79.966331</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hultquist, D.E.</Author>
-<Author>Moyer, R.W.</Author>
-<Author>Boyer, P.D.</Author>
-</Authors>
-<Citation>Biochemistry 5, 322-331, 1966</Citation>
-<Title>The preparation and characterization of 1-phosphohistidine and 3-phosphohistidine.</Title>
-<Xref>DOI:10.1021/bi00865a041</Xref>
-<Xref>PMID:5938947</Xref>
-<Note>the diagram page 330 indicates that what the authors would call "1-phosphohistidine" corresponds to pros-phosphohistidine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hultquist, D.E.</Author>
-</Authors>
-<Citation>Biochim. Biophys. Acta 153, 329-340, 1968</Citation>
-<Title>The preparation and characterization of phosphorylated derivatives of histidine.</Title>
-<Xref>DOI:10.1016/0005-2728(68)90078-9</Xref>
-<Xref>PMID:5642389</Xref>
-<Note>chemical synthesis; chemical characterization; spectrographic characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Anonymous />
-<Group>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN)</Group>
-</Authors>
-<Citation>Eur. J. Biochem. 138, 9-37, 1984</Citation>
-<Title>Nomenclature and symbolism for amino acids and peptides. Recommendations 1983.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1984.tb07877.x</Xref>
-<Xref>PMID:6692818</Xref>
-<Note>tele-, tau-, and pros-, pi-, nomenclature</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Herzberg, O.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, September 1992</Citation>
-<Description>Histidine-containing phosphocarrier protein HPr mutant with Met 51 replaced by Val and Ser 83 replaced by Cys (M51V, S83C).</Description>
-<Xref>PDB:2HPR</Xref>
-<Note>X-ray diffraction, 2.0 angstroms; the description is taken from the PDB COMPND record</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Herzberg, O.</Author>
-<Author>Reddy, P.</Author>
-<Author>Sutrina, S.</Author>
-<Author>Saier Jr., M.H.</Author>
-<Author>Reizer, J.</Author>
-<Author>Kapadia, G.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 89, 2499-2503, 1992</Citation>
-<Title>Structure of the histidine-containing phosphocarrier protein HPr from Bacillus subtilis at 2.0-angstrom resolution.</Title>
-<Xref>DOI:10.1073/pnas.89.6.2499</Xref>
-<Xref>PMID:1549615</Xref>
-<Note>X-ray diffraction, 2.0 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Rajagopal, P.</Author>
-<Author>Waygood, E.B.</Author>
-<Author>Klevit, R.E.</Author>
-</Authors>
-<Citation>Biochemistry 33, 15271-15282, 1994</Citation>
-<Title>Structural consequences of histidine phosphorylation: NMR characterization of the phosphohistidine form of histidine-containing protein from Bacillus subtilis and Escherichia coli.</Title>
-<Xref>DOI:10.1021/bi00255a008</Xref>
-<Xref>PMID:7803390</Xref>
-<Note>conformation by (1)H-NMR</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Jones, B.E.</Author>
-<Author>Rajagopal, P.</Author>
-<Author>Klevit, R.E.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, May 1996</Citation>
-<Description>Refined NMR structure of phosphocarrier histidine containing protein from Bacillus subtilis.</Description>
-<Xref>PDB:2HID</Xref>
-<Note>conformation by (1)H-NMR</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Morera, S.</Author>
-<Author>Chiadmi, M.</Author>
-<Author>LeBras, G.</Author>
-<Author>Lascu, I.</Author>
-<Author>Janin, J.</Author>
-</Authors>
-<Citation>Biochemistry 34, 11062-11070, 1995</Citation>
-<Title>Mechanism of phosphate transfer by nucleoside diphosphate kinase: X-ray structures of the phosphohistidine intermediate of the enzymes from Drosophila and Dictyostelium.</Title>
-<Xref>DOI:10.1021/bi00035a011</Xref>
-<Xref>PMID:7669763</Xref>
-<Note>X-ray diffraction, 2.2 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Janin, J.</Author>
-<Author>Chiadmi, M.</Author>
-<Author>Morera, S.</Author>
-<Author>LeBras, G.</Author>
-<Author>Lascu, I.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, April 1995</Citation>
-<Description>Nucleoside diphosphate kinase (E.C. 2.7.4.6).</Description>
-<Xref>PDB:1NSQ</Xref>
-<Note>X-ray diffraction, 2.2 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Khan, S.R.</Author>
-<Author>Deutscher, J.</Author>
-<Author>Vishwakarma, R.A.</Author>
-<Author>Monedero, V.</Author>
-<Author>Bhatnagar, N.B.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 268, 521-530, 2001</Citation>
-<Title>The ptsH gene from Bacillus thuringiensis israelensis. Characterization of a new phosphorylation site on the protein HPr.</Title>
-<Xref>DOI:10.1046/j.1432-1327.2001.01878</Xref>
-<Xref>PMID:11168390</Xref>
-<Note>alternate tele-phosphorylation of a histidine, normally pros-phosphorylated, inactivates an enzyme; methods for distinguishing the isomers</Note>
-</ReferenceBlock>
-<Comment>In the older biochemical literature this is usually called histidine-1-phosphate. See also RESID:AA0035.</Comment>
-<Comment>The crystallographic designation for the substituted nitrogen is delta-1, D1.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>protein-histidine pros-kinase (EC 2.7.3.11)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>H</SequenceSpec>
-<Xref>GO:0018106</Xref>
-<Xref>GO:0018328</Xref>
-<Xref>PSI-MOD:00045</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>phosphohistidine</Keyword>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="act_site__pros-phosphohistidine intermediate__h">ACT_SITE Pros-phosphohistidine intermediate</Feature>
-<Feature type="UniProt" key="mod_res__pros-phosphohistidine__h">MOD_RES Pros-phosphohistidine</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="act_site__phosphohistidine intermediate__h">ACT_SITE Phosphohistidine intermediate</Feature>
-<Note>this UniProt feature is used when the isomeric structure has not been determined</Note>
-</FeatureNote>
-<FeatureNote>
-<Feature type="UniProt" key="mod_res__phosphohistidine__h">MOD_RES Phosphohistidine</Feature>
-<Note>this UniProt feature is used when the isomeric structure has not been determined</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0036.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0036.PDB" />
-</Entry>
-<Entry id="AA0037">
-<Header>
-<Code>AA0037</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-phospho-L-serine</Name>
-<AlternateName>2-amino-3-hydroxypropanoic acid 3-phosphate</AlternateName>
-<AlternateName>2-azanyl-3-(phosphonooxy)propanoic acid</AlternateName>
-<AlternateName>O-phosphonoserine</AlternateName>
-<AlternateName>O3-phosphoserine</AlternateName>
-<AlternateName>serine phosphate ester</AlternateName>
-<SystematicName>(2S)-2-amino-3-(phosphonooxy)propanoic acid</SystematicName>
-<Xref>CAS:407-41-0</Xref>
-<Xref>ChEBI:45522</Xref>
-<Xref>PDBHET:SEP</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 6 N 1 O 5 P 1</Formula>
-<Weight type="chemical">167.06</Weight>
-<Weight type="physical">166.998359</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 0 H 1 N 0 O 3 P 1</Formula>
-<Weight type="chemical">79.98</Weight>
-<Weight type="physical">79.966331</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lipmann, F.A.</Author>
-<Author>Levene, P.A.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 98, 109-114, 1932</Citation>
-<Title>Serinephosphoric acid obtained on hydrolysis of vitellinic acid.</Title>
-<Note>phosphoserine isolated from a protein hydrolysate</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fischer, E.H.</Author>
-<Author>Graves, D.J.</Author>
-<Author>Crittenden, E.R.</Author>
-<Author>Krebs, E.G.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 234, 1698-1704, 1959</Citation>
-<Title>Structure of the site phosphorylated in the phosphorylase b to a reaction.</Title>
-<Xref>PMID:13672948</Xref>
-<Note>radiolabeling, determination of peptide sequence, demonstration of specific enzymatic production and removal</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Clark, R.C.</Author>
-</Authors>
-<Citation>Int. J. Biochem. 17, 983-988, 1985</Citation>
-<Title>The primary structure of avian phosvitins. Contributions through the Edman degradation of methylmercaptovitins prepared from the constituent phosphoproteins.</Title>
-<Xref>DOI:10.1016/0020-711X(85)90243-5</Xref>
-<Xref>PMID:4065410</Xref>
-<Note>phosphoserine converted to dl-S-methylcysteine for phenylthiohydantoin identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Price, P.A.</Author>
-<Author>Rice, J.S.</Author>
-<Author>Williamson, M.K.</Author>
-</Authors>
-<Citation>Protein Sci. 3, 822-830, 1994</Citation>
-<Title>Conserved phosphorylation of serines in the Ser-X-Glu/Ser(P) sequences of the vitamin K-dependent matrix Gla protein from shark, lamb, rat, cow, and human.</Title>
-<Xref>DOI:10.1002/pro.5560030511</Xref>
-<Xref>PMID:8061611</Xref>
-<Note>improved methodology for conversion to dl-S-methylcysteine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Knight, Z.A.</Author>
-<Author>Schilling, B.</Author>
-<Author>Row, R.H.</Author>
-<Author>Kenski, D.M.</Author>
-<Author>Gibson, B.W.</Author>
-<Author>Shokat, K.M.</Author>
-</Authors>
-<Citation>Nature Biotechnol. 21, 1047-1054, 2003</Citation>
-<Title>Phosphospecific proteolysis for mapping sites of protein phosphorylation.</Title>
-<Xref>DOI:10.1038/nbt863</Xref>
-<Xref>PMID:12923550</Xref>
-<Note>method for converting phosphoserine and phosphothreonine to analogs of lysine for enzymatic analysis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Park, H.S.</Author>
-<Author>Hohn, M.J.</Author>
-<Author>Umehara, T.</Author>
-<Author>Guo, L.T.</Author>
-<Author>Osborne, E.M.</Author>
-<Author>Benner, J.</Author>
-<Author>Noren, C.J.</Author>
-<Author>Rinehart, J.</Author>
-<Author>Söll, D.</Author>
-</Authors>
-<Citation>Science 333, 1151-1154, 2011</Citation>
-<Title>Expanding the genetic code of Escherichia coli with phosphoserine.</Title>
-<Xref>DOI:10.1126/science.1207203</Xref>
-<Xref>PMID:21868676</Xref>
-<Note>engineered system for encoding phosphoserine as a pretranslational modification</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>protein-serine kinase (EC 2.7.1.37)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>GO:0018105</Xref>
-<Xref>GO:0018331</Xref>
-<Xref>PSI-MOD:00046</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="act_site__phosphoserine intermediate__s">ACT_SITE Phosphoserine intermediate</Feature>
-<Feature type="UniProt" key="mod_res__phosphoserine__s">MOD_RES Phosphoserine</Feature>
-</Features>
-<Image src="/images/AA0037.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0037.PDB" />
-</Entry>
-<Entry id="AA0038">
-<Header>
-<Code>AA0038</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-phospho-L-threonine</Name>
-<AlternateName>2-amino-3-hydroxybutanoic acid 3-phosphate</AlternateName>
-<AlternateName>2-azanyl-3-(phosphonooxy)butanoic acid</AlternateName>
-<AlternateName>O3-phosphothreonine</AlternateName>
-<AlternateName>threonine phosphate ester</AlternateName>
-<SystematicName>(2S,3R)-2-amino-3-(phosphonooxy)butanoic acid</SystematicName>
-<Xref>CAS:1114-81-4</Xref>
-<Xref>ChEBI:61971</Xref>
-<Xref>PDBHET:TPO</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 8 N 1 O 5 P 1</Formula>
-<Weight type="chemical">181.08</Weight>
-<Weight type="physical">181.014009</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0017">
-<Formula>C 0 H 1 N 0 O 3 P 1</Formula>
-<Weight type="chemical">79.98</Weight>
-<Weight type="physical">79.966331</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lindberg, R.A.</Author>
-<Author>Fischer, W.H.</Author>
-<Author>Hunter, T.</Author>
-</Authors>
-<Citation>Oncogene 8, 351-359, 1993</Citation>
-<Title>Characterization of a human protein threonine kinase isolated by screening an expression library with antibodies to phosphotyrosine.</Title>
-<Xref>PMID:7678926</Xref>
-<Note>antibody detection</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Knight, Z.A.</Author>
-<Author>Schilling, B.</Author>
-<Author>Row, R.H.</Author>
-<Author>Kenski, D.M.</Author>
-<Author>Gibson, B.W.</Author>
-<Author>Shokat, K.M.</Author>
-</Authors>
-<Citation>Nature Biotechnol. 21, 1047-1054, 2003</Citation>
-<Title>Phosphospecific proteolysis for mapping sites of protein phosphorylation.</Title>
-<Xref>DOI:10.1038/nbt863</Xref>
-<Xref>PMID:12923550</Xref>
-<Note>method for converting phosphoserine and phosphothreonine to analogs of lysine for enzymatic analysis</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>protein-threonine kinase (EC 2.7.1.37)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>T</SequenceSpec>
-<Xref>GO:0018107</Xref>
-<Xref>GO:0018333</Xref>
-<Xref>PSI-MOD:00047</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__phosphothreonine__t">MOD_RES Phosphothreonine</Feature>
-</Features>
-<Image src="/images/AA0038.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0038.PDB" />
-</Entry>
-<Entry id="AA0039">
-<Header>
-<Code>AA0039</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O4'-phospho-L-tyrosine</Name>
-<AlternateName>2-amino-3-(4-hydroxyphenyl)propanoic acid 4'-phosphate</AlternateName>
-<AlternateName>2-azanyl-3-(4-phosphonooxyphenyl)propanoic acid</AlternateName>
-<AlternateName>O4-phosphotyrosine</AlternateName>
-<AlternateName>tyrosine phosphate</AlternateName>
-<SystematicName>(2S)-2-amino-3-(4-phosphonooxyphenyl)propanoic acid</SystematicName>
-<Xref>CAS:21820-51-9</Xref>
-<Xref>ChEBI:61972</Xref>
-<Xref>PDBHET:PTR</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 10 N 1 O 5 P 1</Formula>
-<Weight type="chemical">243.15</Weight>
-<Weight type="physical">243.029659</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0019">
-<Formula>C 0 H 1 N 0 O 3 P 1</Formula>
-<Weight type="chemical">79.98</Weight>
-<Weight type="physical">79.966331</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Aebersold, R.</Author>
-<Author>Watts, J.D.</Author>
-<Author>Morrison, H.D.</Author>
-<Author>Bures, E.J.</Author>
-</Authors>
-<Citation>Anal. Biochem. 199, 51-60, 1991</Citation>
-<Title>Determination of the site of tyrosine phosphorylation at the low picomole level by automated solid-phase sequence analysis.</Title>
-<Xref>DOI:10.1016/0003-2697(91)90268-X</Xref>
-<Xref>PMID:1725475</Xref>
-<Note>chromatographic detection</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wolfender, J.L.</Author>
-<Author>Chu, F.</Author>
-<Author>Ball, H.</Author>
-<Author>Wolfender, F.</Author>
-<Author>Fainzilber, M.</Author>
-<Author>Baldwin, M.A.</Author>
-<Author>Burlingame, A.L.</Author>
-</Authors>
-<Citation>J. Mass Spectrom. 34, 447-454, 1999</Citation>
-<Title>Identification of tyrosine sulfation in Conus pennaceus conotoxins alpha-PnIA and alpha-PnIB: further investigation of labile sulfo- and phosphopeptides by electrospray, matrix-assisted laser desorption/ionization (MALDI) and atmospheric pressure MALDI mass spectrometry.</Title>
-<Xref>DOI:10.1002/(SICI)1096-9888(199904)34:4&lt;447::AID-JMS801&gt;3.3.CO;2-T</Xref>
-<Xref>PMID:10226369</Xref>
-<Note>attempt to distinguish between the essentially isobaric protonated forms of phosphotyrosine and sulfotyrosine (see RESID:AA0172) by negative ion mode MALDI</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>protein-tyrosine kinase (EC 2.7.1.112)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>Y</SequenceSpec>
-<Xref>GO:0018108</Xref>
-<Xref>GO:0018334</Xref>
-<Xref>PSI-MOD:00048</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__phosphotyrosine__y">MOD_RES Phosphotyrosine</Feature>
-</Features>
-<Image src="/images/AA0039.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0039.PDB" />
-</Entry>
-<Entry id="AA0040">
-<Header>
-<Code>AA0040</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>30-Jun-2005</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>2'-[3-carboxamido-3-(trimethylammonio)propyl]-L-histidine</Name>
-<AlternateName>(3-[4-(2-amino-2-carboxy-ethyl)-1H-imidazol-2-yl]-1-carbamoyl-propyl)-trimethylammonium</AlternateName>
-<AlternateName>1-azanyl-4-(4-[2-azanyl-2-carboxyethyl]-1H-imidazol-2-yl)-N,N,N-trimethyl-1-oxobutan-2-azanium</AlternateName>
-<AlternateName>2-amino-3-[[2-(3-amino-3-carbamoyl-prop-1-enyl)-1,1,3-trimethyl-2,3-dihydroimidazol-5-yl]]propanoic acid</AlternateName>
-<AlternateName>2-amino-4-[[5-(2-amino-2-carboxylato-ethyl)-1,1,3-trimethyl-2,3-dihydroimidazol-2-yl]]but-3-enamide</AlternateName>
-<AlternateName>2-[(R)-3-carboxamido-3-(trimethylammonio)propyl]-4-((S)-2-amino-2-carboxyethyl)-1H-imidazole</AlternateName>
-<AlternateName>2-[3-carboxamido-3-(trimethylammonio)propyl]histidine</AlternateName>
-<AlternateName>alpha-(aminocarbonyl)-4-(2-amino-2-carboxyethyl)-N,N,N-trimethyl-1H-imidazole-2-propanaminium</AlternateName>
-<AlternateName>diphthamide</AlternateName>
-<SystematicName>(2R)-1-amino-4-(4-[(2S)-2-amino-2-carboxyethyl]-1H-imidazol-2-yl)-N,N,N-trimethyl-1-oxobutan-2-aminium</SystematicName>
-<Xref>CAS:75645-22-6</Xref>
-<Xref>ChEBI:16692</Xref>
-<Xref>PDBHET:DDE</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 13 H 22 N 5 O 2</Formula>
-<FormalCharge>1+</FormalCharge>
-<Weight type="chemical">280.35</Weight>
-<Weight type="physical">280.176801</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0009">
-<Formula>C 7 H 15 N 2 O 1</Formula>
-<FormalCharge>1+</FormalCharge>
-<Weight type="chemical">143.21</Weight>
-<Weight type="physical">143.117890</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Van Ness, B.G.</Author>
-<Author>Howard, J.B.</Author>
-<Author>Bodley, J.W.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 255, 10710-10716, 1980</Citation>
-<Title>ADP-ribosylation of elongation factor 2 by diphtheria toxin. NMR spectra and proposed structures of ribosyl-diphthamide and its hydrolysis products.</Title>
-<Xref>PMID:7430147</Xref>
-<Note>(1)H-NMR and (13)C-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Jorgensen, R.</Author>
-<Author>Yates, S.P.</Author>
-<Author>Teal, D.J.</Author>
-<Author>Nilsson, J.</Author>
-<Author>Prentice, G.A.</Author>
-<Author>Merrill, A.R.</Author>
-<Author>Andersen, G.R.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 279, 45919-45925, 2004</Citation>
-<Title>Crystal structure of ADP-ribosylated ribosomal translocase from Saccharomyces cerevisiae.</Title>
-<Xref>DOI:10.1074/jbc.M406218200</Xref>
-<Xref>PMID:15316019</Xref>
-<Note>X-ray diffraction, 2.6 angstroms; resolution of second chiral center</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Jorgensen, R.</Author>
-<Author>Yates, S.P.</Author>
-<Author>Nilsson, J.</Author>
-<Author>Prentice, G.A.</Author>
-<Author>Teal, D.J.</Author>
-<Author>Merrill, A.R.</Author>
-<Author>Andersen, G.R.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, July 2004</Citation>
-<Description>Crystal structure of ADP-ribosylated ribosomal translocase from Saccharomyces cerevisiae.</Description>
-<Xref>PDB:1U2R</Xref>
-<Note>X-ray diffraction, 2.6 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Zhang, Y.</Author>
-<Author>Zhu, X.</Author>
-<Author>Torelli, A.T.</Author>
-<Author>Lee, M.</Author>
-<Author>Dzikovski, B.</Author>
-<Author>Koralewski, R.M.</Author>
-<Author>Wang, E.</Author>
-<Author>Freed, J.</Author>
-<Author>Krebs, C.</Author>
-<Author>Ealick, S.E.</Author>
-<Author>Lin, H.</Author>
-</Authors>
-<Citation>Nature 465, 891-896, 2010</Citation>
-<Title>Diphthamide biosynthesis requires an organic radical generated by an iron-sulphur enzyme.</Title>
-<Xref>DOI:10.1038/nature09138</Xref>
-<Xref>PMID:20559380</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Dong, M.</Author>
-<Author>Kathiresan, V.</Author>
-<Author>Fenwick, M.K.</Author>
-<Author>Torelli, A.T.</Author>
-<Author>Zhang, Y.</Author>
-<Author>Caranto, J.D.</Author>
-<Author>Dzikovski, B.</Author>
-<Author>Sharma, A.</Author>
-<Author>Lancaster, K.M.</Author>
-<Author>Freed, J.H.</Author>
-<Author>Ealick, S.E.</Author>
-<Author>Hoffman, B.M.</Author>
-<Author>Lin, H.</Author>
-</Authors>
-<Citation>Science 359, 1247-1250, 2018</Citation>
-<Title>Organometallic and radical intermediates reveal mechanism of diphthamide biosynthesis.</Title>
-<Xref>DOI:10.1126/science.aao6595</Xref>
-<Xref>PMID:29590073</Xref>
-<Note>electron paramagnetic resonance spectroscopy; electron nuclear double-resonance spectroscopy</Note>
-</ReferenceBlock>
-<Comment>Diphthamide appears to occur uniquely in translation elongation factor eEF-2.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>2-(3-amino-3-carboxypropyl)histidine synthase</EnzymeName>
-<EnzymeName>S-adenosyl-L-methionine:L-histidine-[translation elongation factor 2] 2-[(3S)-3-amino-3-carboxypropyl]transferase (EC 2.5.1.108)</EnzymeName>
-<EnzymeName>diphthine synthase</EnzymeName>
-<EnzymeName>S-adenosyl-L-methionine:2-[(3S)-3-carboxy-3-aminopropyl]-L-histidine-[translation elongation factor 2] methyltransferase (diphthine-[translation elongation factor 2]-forming) (EC 2.1.1.98)</EnzymeName>
-<EnzymeName>diphthine--ammonia ligase</EnzymeName>
-<EnzymeName>diphthine-[translation elongation factor 2]:ammonia ligase (AMP-forming) (EC 6.3.1.14)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>H</SequenceSpec>
-<Xref>GO:0006471</Xref>
-<Xref>GO:0017183</Xref>
-<Xref>PSI-MOD:00049</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>diphthamide</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__diphthamide__h">MOD_RES Diphthamide</Feature>
-</Features>
-<Image src="/images/AA0040.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0040.PDB" />
-</Entry>
-<Entry id="AA0041">
-<Header>
-<Code>AA0041</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-acetyl-L-alanine</Name>
-<AlternateName>2-(acetylamino)propanoic acid</AlternateName>
-<AlternateName>2-(acetylazanyl)propanoic acid</AlternateName>
-<AlternateName>acetylalanine</AlternateName>
-<SystematicName>(2S)-2-(acetamido)propanoic acid</SystematicName>
-<Xref>CAS:97-69-8</Xref>
-<Xref>ChEBI:61920</Xref>
-<Xref>PDBHET:ACE</Xref>
-<Xref>PDBHET:AYA</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 8 N 1 O 2</Formula>
-<Weight type="chemical">114.12</Weight>
-<Weight type="physical">114.055504</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0001">
-<Formula>C 2 H 2 N 0 O 1</Formula>
-<Weight type="chemical">42.04</Weight>
-<Weight type="physical">42.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Coffee, C.J.</Author>
-<Author>Bradshaw, R.A.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 248, 3305-3312, 1973</Citation>
-<Title>Carp muscle calcium-binding protein. I. Characterization of the tryptic peptides and the complete amino acid sequence of component B.</Title>
-<Xref>PMID:4700462</Xref>
-<Note>chemical characterization and mass spectrometric identification; the first page number in the PubMed citation is corrected</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kretsinger, R.H.</Author>
-<Author>Nockolds, C.E.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 248, 3313-3326, 1973</Citation>
-<Title>Carp muscle calcium-binding protein. II. Structure determination and general description.</Title>
-<Xref>PMID:4700463</Xref>
-<Note>X-ray diffraction, 1.85 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wittmann-Liebold, B.</Author>
-<Author>Greuer, B.</Author>
-</Authors>
-<Citation>FEBS Lett. 95, 91-98, 1978</Citation>
-<Title>The primary structure of protein S5 from the small subunit of the Escherichia coli ribosome.</Title>
-<Xref>DOI:10.1016/0014-5793(78)80059-3</Xref>
-<Xref>PMID:363452</Xref>
-<Note>chemical characterization and mass spectrometric identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Swain, A.L.</Author>
-<Author>Kretsinger, R.H.</Author>
-<Author>Amma, E.L.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, January 1990</Citation>
-<Description>Restrained least squares refinement of native (calcium) and cadmium-substituted carp parvalbumin using X-ray crystallographic data at 1.6-A resolution.</Description>
-<Xref>PDB:5CPV</Xref>
-<Note>X-ray diffraction, 1.6 angstroms</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>N-terminal amino-acid Nα-acetyltransferase NatA</EnzymeName>
-<EnzymeName>acetyl-CoA:ribosomal-protein-L-alanine N-acetyltransferase (EC 2.3.1.128)</EnzymeName>
-<EnzymeName>acetyl-CoA:N-terminal-Gly/Ala/Ser/Val/Cys/Thr-[protein] Nα-acetyltransferase (EC 2.3.1.256)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>A</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0017189</Xref>
-<Xref>PSI-MOD:00050</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>acetylated amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n-acetylalanine__a">MOD_RES N-acetylalanine</Feature>
-</Features>
-<Image src="/images/AA0041.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0041.PDB" />
-</Entry>
-<Entry id="AA0042">
-<Header>
-<Code>AA0042</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-acetyl-L-aspartic acid</Name>
-<AlternateName>2-(acetylamino)butanedioic acid</AlternateName>
-<AlternateName>2-(acetylazanyl)butanedioic acid</AlternateName>
-<AlternateName>acetylaspartic acid</AlternateName>
-<SystematicName>(2S)-2-(acetamido)butanedioic acid</SystematicName>
-<Xref>CAS:997-55-7</Xref>
-<Xref>ChEBI:21547</Xref>
-<Xref>PDBHET:ACE</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 8 N 1 O 4</Formula>
-<Weight type="chemical">158.13</Weight>
-<Weight type="physical">158.045333</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0004">
-<Formula>C 2 H 2 N 0 O 1</Formula>
-<Weight type="chemical">42.04</Weight>
-<Weight type="physical">42.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kabsch, W.</Author>
-<Author>Mannherz, H.G.</Author>
-<Author>Suck, D.</Author>
-<Author>Pai, E.</Author>
-<Author>Holmes, K.C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, March 1991</Citation>
-<Description>Atomic structure of the actin: DNase I complex.</Description>
-<Xref>PDB:1ATN</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kabsch, W.</Author>
-<Author>Mannherz, H.G.</Author>
-<Author>Suck, D.</Author>
-<Author>Pai, E.F.</Author>
-<Author>Holmes, K.C.</Author>
-</Authors>
-<Citation>Nature 347, 37-44, 1990</Citation>
-<Title>Atomic structure of the actin: DNase I complex.</Title>
-<Xref>DOI:10.1038/347037a0</Xref>
-<Xref>PMID:2395459</Xref>
-<Note>X-ray diffraction, 2.8 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Martin, P.</Author>
-<Author>Edwards, B.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, April 1992</Citation>
-<Description>The structure of residues 7-16 of the Aalpha-chain of human fibrinogen bound to bovine thrombin at 2.3-A resolution.</Description>
-<Xref>PDB:1BBR</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Martin, P.D.</Author>
-<Author>Robertson, W.</Author>
-<Author>Turk, D.</Author>
-<Author>Huber, R.</Author>
-<Author>Bode, W.</Author>
-<Author>Edwards, B.F.P.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 267, 7911-7920, 1992</Citation>
-<Title>The structure of residues 7-16 of the Aalpha-chain of human fibrinogen bound to bovine thrombin at 2.3-angstroms resolution.</Title>
-<Xref>PMID:1560020</Xref>
-<Note>X-ray diffraction, 2.3 angstroms</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>D</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0017190</Xref>
-<Xref>PSI-MOD:00051</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>acetylated amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n-acetylaspartate__d">MOD_RES N-acetylaspartate</Feature>
-</Features>
-<Image src="/images/AA0042.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0042.PDB" />
-</Entry>
-<Entry id="AA0043">
-<Header>
-<Code>AA0043</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-acetyl-L-cysteine</Name>
-<AlternateName>2-acetylamino-3-mercaptopropanoic acid</AlternateName>
-<AlternateName>2-acetylamino-3-sulfanylpropanoic acid</AlternateName>
-<AlternateName>2-acetylazanyl-3-sulfanylpropanoic acid</AlternateName>
-<AlternateName>N-acetylcysteine</AlternateName>
-<SystematicName>(2R)-2-acetamido-3-sulfanylpropanoic acid</SystematicName>
-<Xref>CAS:616-91-1</Xref>
-<Xref>ChEBI:28939</Xref>
-<Xref>PDBHET:ACE</Xref>
-<Xref>PDBHET:SC2</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 8 N 1 O 2 S 1</Formula>
-<Weight type="chemical">146.18</Weight>
-<Weight type="physical">146.027574</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 2 H 2 N 0 O 1 S 0</Formula>
-<Weight type="chemical">42.04</Weight>
-<Weight type="physical">42.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Grand, R.J.</Author>
-<Author>Perry, S.V.</Author>
-</Authors>
-<Citation>Biochem. J. 211, 267-272, 1983</Citation>
-<Title>Preparation of the alkali and P light chains of chicken gizzard myosin. Amino acid sequence of the alkali light chain.</Title>
-<Xref>PMID:6870825</Xref>
-<Note>(1)H-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Strauch, A.R.</Author>
-<Author>Rubenstein, P.A.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 259, 7224-7229, 1984</Citation>
-<Title>A vascular smooth muscle alpha-isoactin biosynthetic intermediate in BC3H1 cells. Identification of acetylcysteine at the NH2 terminus.</Title>
-<Xref>PMID:6725286</Xref>
-<Note>radioisotope labeling; identification of transient modification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hasegawa, Y.</Author>
-<Author>Ueda, Y.</Author>
-<Author>Watanabe, M.</Author>
-<Author>Morita, F.</Author>
-</Authors>
-<Citation>J. Biochem. 111, 798-803, 1992</Citation>
-<Title>Studies on amino acid sequences of two isoforms of 17-kDa essential light chain of smooth muscle myosin from porcine aorta media.</Title>
-<Xref>PMID:1500421</Xref>
-<Note>mass spectrometric identification</Note>
-</ReferenceBlock>
-<Comment>See also RESID:AA0044.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>N-terminal amino-acid Nα-acetyltransferase NatA</EnzymeName>
-<EnzymeName>acetyl-CoA:N-terminal-Gly/Ala/Ser/Val/Cys/Thr-[protein] Nα-acetyltransferase (EC 2.3.1.256)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Condition>incidental to RESID:AA0223</Condition>
-<Xref>GO:0018275</Xref>
-<Xref>PSI-MOD:00052</Xref>
-<Xref>PSI-MOD:00897</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>acetylated amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n-acetylcysteine__c">MOD_RES N-acetylcysteine</Feature>
-</Features>
-<Image src="/images/AA0043.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0043.PDB" />
-</Entry>
-<Entry id="AA0044">
-<Header>
-<Code>AA0044</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-acetyl-L-glutamic acid</Name>
-<AlternateName>2-(acetylamino)pentanedioic acid</AlternateName>
-<AlternateName>2-(acetylazanyl)pentanedioic acid</AlternateName>
-<AlternateName>acetylglutamic acid</AlternateName>
-<SystematicName>(2S)-2-(acetamido)pentanedioic acid</SystematicName>
-<Xref>CAS:1188-37-0</Xref>
-<Xref>ChEBI:17533</Xref>
-<Xref>PDBHET:ACE</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 10 N 1 O 4</Formula>
-<Weight type="chemical">172.16</Weight>
-<Weight type="physical">172.060983</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0006">
-<Formula>C 2 H 2 N 0 O 1</Formula>
-<Weight type="chemical">42.04</Weight>
-<Weight type="physical">42.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Strauch, A.R.</Author>
-<Author>Rubenstein, P.A.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 259, 7224-7229, 1984</Citation>
-<Title>A vascular smooth muscle alpha-isoactin biosynthetic intermediate in BC3H1 cells. Identification of acetylcysteine at the NH2 terminus.</Title>
-<Xref>PMID:6725286</Xref>
-<Note>identification after a transient primary acetylation</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hill, C.P.</Author>
-<Author>Anderson, D.H.</Author>
-<Author>Wesson, L.</Author>
-<Author>DeGrado, W.F.</Author>
-<Author>Eisenberg, D.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, July 1990</Citation>
-<Description>Crystal structure of alpha1: implications for protein design.</Description>
-<Xref>PDB:1AL1</Xref>
-<Note>synthetic peptide; X-ray diffraction, 2.7 angstroms</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>E</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Condition>incidental to RESID:AA0043</Condition>
-<Xref>GO:0018002</Xref>
-<Xref>PSI-MOD:00053</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>acetylated amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n-acetylglutamate__e">MOD_RES N-acetylglutamate</Feature>
-</Features>
-<Image src="/images/AA0044.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0044.PDB" />
-</Entry>
-<Entry id="AA0045">
-<Header>
-<Code>AA0045</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-acetyl-L-glutamine</Name>
-<AlternateName>2-acetylamino-5-amino-5-oxopentanoic acid</AlternateName>
-<AlternateName>2-acetylamino-5-pentanediamic acid</AlternateName>
-<AlternateName>2-acetylazanyl-5-azanyl-5-oxopentanoic acid</AlternateName>
-<AlternateName>acetylglutamine</AlternateName>
-<SystematicName>(2S)-2-acetamido-5-pentanediamic acid</SystematicName>
-<Xref>CAS:2490-97-3</Xref>
-<Xref>ChEBI:21553</Xref>
-<Xref>PDBHET:ACE</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 11 N 2 O 3</Formula>
-<Weight type="chemical">171.18</Weight>
-<Weight type="physical">171.076967</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0007">
-<Formula>C 2 H 2 N 0 O 1</Formula>
-<Weight type="chemical">42.04</Weight>
-<Weight type="physical">42.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Edmundson, A.B.</Author>
-<Author>Harris, D.L.</Author>
-<Author>Fan, Z.C.</Author>
-<Author>Guddat, L.W.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, February 1993</Citation>
-<Description>Principles and pitfalls in designing site-directed peptide ligands.</Description>
-<Xref>PDB:1MCC</Xref>
-<Note>synthetic peptide; X-ray diffraction, 2.7 angstroms</Note>
-</ReferenceBlock>
-<Comment>The occurrence of this modification has not been confirmed. Formerly, its annotation in sequence databases was due to either the misidentification of 2-pyrrolidone-5-carboxylic acid, or inappropriate homolog comparisons when proteolytic modification was more probable.</Comment>
-<SequenceCode>
-<SequenceSpec>Q</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0017192</Xref>
-<Xref>PSI-MOD:00054</Xref>
-</SequenceCode>
-<Source>deprecated</Source>
-<Keywords>
-<Keyword>acetylated amino end</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this dubious modification is not currently annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0045.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0045.PDB" />
-</Entry>
-<Entry id="AA0046">
-<Header>
-<Code>AA0046</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-acetylglycine</Name>
-<AlternateName>(acetylamino)acetic acid</AlternateName>
-<AlternateName>(acetylazanyl)ethanoic acid</AlternateName>
-<AlternateName>2-(acetylamino)ethanoic acid</AlternateName>
-<AlternateName>aceturic acid</AlternateName>
-<SystematicName>2-(acetamido)ethanoic acid</SystematicName>
-<Xref>CAS:543-24-8</Xref>
-<Xref>ChEBI:61888</Xref>
-<Xref>PDBHET:ACE</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 6 N 1 O 2</Formula>
-<Weight type="chemical">100.10</Weight>
-<Weight type="physical">100.039853</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0008">
-<Formula>C 2 H 2 N 0 O 1</Formula>
-<Weight type="chemical">42.04</Weight>
-<Weight type="physical">42.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Luo, Y.</Author>
-<Author>Brayer, G.D.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, August 1994</Citation>
-<Description>High-resolution three-dimensional structure of horse heart cytochrome c.</Description>
-<Xref>PDB:1HRC</Xref>
-<Note>X-ray diffraction, 1.9 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Dickerson, R.E.</Author>
-<Author>Takano, T.</Author>
-<Author>Eisenberg, D.</Author>
-<Author>Kallai, O.B.</Author>
-<Author>Samson, L.</Author>
-<Author>Cooper, A.</Author>
-<Author>Margoliash, E.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 246, 1511-1535, 1971</Citation>
-<Title>Ferricytochrome c. I. General features of the horse and bonito proteins at 2.8 A resolution.</Title>
-<Xref>PMID:5545094</Xref>
-<Note>X-ray diffraction, 2.8 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Tsunasawa, S.</Author>
-<Author>Narita, K.</Author>
-</Authors>
-<Citation>J. Biochem. 92, 607-613, 1982</Citation>
-<Title>Micro-identification of amino-terminal acetylamino acids in proteins.</Title>
-<Xref>PMID:6754709</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Palmiter, R.D.</Author>
-<Author>Gagnon, J.</Author>
-<Author>Walsh, K.A.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 75, 94-98, 1978</Citation>
-<Title>Ovalbumin: a secreted protein without a transient hydrophobic leader sequence.</Title>
-<Xref>DOI:10.1073/pnas.75.1.94</Xref>
-<Xref>PMID:272676</Xref>
-<Note>biosynthesis</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>N-terminal amino-acid Nα-acetyltransferase NatA</EnzymeName>
-<EnzymeName>acetyl-CoA:N-terminal-Gly/Ala/Ser/Val/Cys/Thr-[protein] Nα-acetyltransferase (EC 2.3.1.256)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>G</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0017193</Xref>
-<Xref>PSI-MOD:00055</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>acetylated amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n-acetylglycine__g">MOD_RES N-acetylglycine</Feature>
-</Features>
-<Image src="/images/AA0046.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0046.PDB" />
-</Entry>
-<Entry id="AA0047">
-<Header>
-<Code>AA0047</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-2001</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-acetyl-L-isoleucine</Name>
-<AlternateName>2-acetylamino-3-methylpentanoic acid</AlternateName>
-<AlternateName>2-acetylazanyl-3-methylpentanoic acid</AlternateName>
-<AlternateName>acetylisoleucine</AlternateName>
-<SystematicName>(2S,3S)-2-acetamido-3-methylpentanoic acid</SystematicName>
-<Xref>CAS:3077-46-1</Xref>
-<Xref>ChEBI:21555</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 8 H 14 N 1 O 2</Formula>
-<Weight type="chemical">156.20</Weight>
-<Weight type="physical">156.102454</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0010">
-<Formula>C 2 H 2 N 0 O 1</Formula>
-<Weight type="chemical">42.04</Weight>
-<Weight type="physical">42.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gowda, L.R.</Author>
-<Author>Savithri, H.S.</Author>
-<Author>Rao, D.R.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 269, 18789-18793, 1994</Citation>
-<Title>The complete primary structure of a unique mannose/glucose-specific lectin from field bean (Dolichos lab lab).</Title>
-<Xref>PMID:8034631</Xref>
-<Note>the authors say a chain is blocked but do not show that it is acetylated</Note>
-</ReferenceBlock>
-<Comment>The occurrence of this modification has not been confirmed.</Comment>
-<SequenceCode>
-<SequenceSpec>I</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0017194</Xref>
-<Xref>PSI-MOD:00056</Xref>
-</SequenceCode>
-<Source>deprecated</Source>
-<Keywords>
-<Keyword>acetylated amino end</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this dubious modification is not currently annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0047.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0047.PDB" />
-</Entry>
-<Entry id="AA0048">
-<Header>
-<Code>AA0048</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>25-Feb-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N2-acetyl-L-lysine</Name>
-<AlternateName>2-acetylamino-6-aminohexanoic acid</AlternateName>
-<AlternateName>2-acetylazanyl-6-azanylhexanoic acid</AlternateName>
-<AlternateName>N2-acetyllysine</AlternateName>
-<SystematicName>(2S)-2-acetamido-6-aminohexanoic acid</SystematicName>
-<Xref>CAS:1946-82-3</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 8 H 15 N 2 O 2</Formula>
-<Weight type="chemical">171.22</Weight>
-<Weight type="physical">171.113353</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 2 H 2 N 0 O 1</Formula>
-<Weight type="chemical">42.04</Weight>
-<Weight type="physical">42.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>McInnes, C.</Author>
-<Author>Sonnichsen, F.D.</Author>
-<Author>Kay, C.M.</Author>
-<Author>Hodges, R.S.</Author>
-<Author>Sykes, B.D.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, August 1993</Citation>
-<Description>NMR solution structure and flexibility of a peptide antigen representing the receptor binding domain of Pseudomonas aeruginosa.</Description>
-<Xref>PDB:1PAJ</Xref>
-<Note>synthetic peptide; (1)H-NMR</Note>
-</ReferenceBlock>
-<Comment>The occurrence of this modification has not been confirmed. The common peptide alpha-N-acetyltransferase does not acetylate basic residues.</Comment>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0017195</Xref>
-<Xref>PSI-MOD:00057</Xref>
-</SequenceCode>
-<Source>deprecated</Source>
-<Keywords>
-<Keyword>acetylated amino end</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this dubious modification is not currently annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0048.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0048.PDB" />
-</Entry>
-<Entry id="AA0049">
-<Header>
-<Code>AA0049</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-acetyl-L-methionine</Name>
-<AlternateName>2-acetylamino-4-(methylsulfanyl)butanoic acid</AlternateName>
-<AlternateName>2-acetylamino-4-(methylthio)butanoic acid</AlternateName>
-<AlternateName>2-acetylazanyl-4-(methylsulfanyl)butanoic acid</AlternateName>
-<AlternateName>acetylmethionine</AlternateName>
-<AlternateName>methionamine</AlternateName>
-<SystematicName>(2S)-2-acetamido-4-(methylsulfanyl)butanoic acid</SystematicName>
-<Xref>CAS:65-82-7</Xref>
-<Xref>ChEBI:21557</Xref>
-<Xref>PDBHET:ACE</Xref>
-<Xref>PDBHET:AME</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 12 N 1 O 2 S 1</Formula>
-<Weight type="chemical">174.24</Weight>
-<Weight type="physical">174.058875</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0013">
-<Formula>C 2 H 2 N 0 O 1 S 0</Formula>
-<Weight type="chemical">42.04</Weight>
-<Weight type="physical">42.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Huang, W.Y.</Author>
-<Author>Chirala, S.S.</Author>
-<Author>Wakil, S.J.</Author>
-</Authors>
-<Citation>Arch. Biochem. Biophys. 314, 45-49, 1994</Citation>
-<Title>Amino-terminal blocking group and sequence of the animal fatty acid synthase.</Title>
-<Xref>DOI:10.1006/abbi.1994.1410</Xref>
-<Xref>PMID:7944406</Xref>
-<Note>chromatographic and chemical characterization; chemical synthesis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Scott, D.C.</Author>
-<Author>Monda, J.K.</Author>
-<Author>Bennett, E.J.</Author>
-<Author>Harper, J.W.</Author>
-<Author>Schulman, B.A.</Author>
-</Authors>
-<Citation>Science 334, 674-678, 2011</Citation>
-<Title>N-terminal acetylation acts as an avidity enhancer within an interconnected multiprotein complex.</Title>
-<Xref>DOI:10.1126/science.1209307</Xref>
-<Xref>PMID:21940857</Xref>
-<Note>mass spectrometric identification; N-acetylmethionine is specifically recognized and required for NEDD8 transfer</Note>
-</ReferenceBlock>
-<Comment>Although appropriate, the keyword "thioether bond" normally does not appear for this amino acid.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>N-terminal methionine N(α)-acetyltransferase NatB</EnzymeName>
-<EnzymeName>acetyl-CoA:N-terminal Met-Asn/Gln/Asp/Glu-[protein] Met-N(α)-acetyltransferase (EC 2.3.1.225)</EnzymeName>
-<EnzymeName>N-terminal methionine N(α)-acetyltransferase NatC</EnzymeName>
-<EnzymeName>acetyl-CoA:N-terminal Met-Leu/Ile/Phe/Trp/Tyr-[protein] Met-N(α)-acetyltransferase (EC 2.3.1.226)</EnzymeName>
-<EnzymeName>N-terminal methionine N(α)-acetyltransferase NatE</EnzymeName>
-<EnzymeName>acetyl-CoA:N-terminal Met-Ala/Ser/Val/Thr/Lys/Leu/Phe/Tyr-[protein] Met-N(α)-acetyltransferase (EC 2.3.1.258)</EnzymeName>
-<EnzymeName>N-terminal methionine N(α)-acetyltransferase NatF</EnzymeName>
-<EnzymeName>acetyl-CoA:N-terminal Met-Lys/Ser/Val/Leu/Gln/Ile/Tyr/Thr-[transmembrane protein] Met-N(α)-acetyltransferase (EC 2.3.1.259)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>M</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0017196</Xref>
-<Xref>PSI-MOD:00058</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>*thioether bond</Keyword>
-<Keyword>acetylated amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n-acetylmethionine__m">MOD_RES N-acetylmethionine</Feature>
-</Features>
-<Image src="/images/AA0049.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0049.PDB" />
-</Entry>
-<Entry id="AA0050">
-<Header>
-<Code>AA0050</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-acetyl-L-proline</Name>
-<AlternateName>1-acetylproline</AlternateName>
-<AlternateName>acetylproline</AlternateName>
-<AlternateName>N-acetylproline</AlternateName>
-<SystematicName>(2S)-1-acetyl-2-pyrrolidinecarboxylic acid</SystematicName>
-<Xref>CAS:68-95-1</Xref>
-<Xref>ChEBI:21560</Xref>
-<Xref>PDBHET:ACE</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 10 N 1 O 2</Formula>
-<Weight type="chemical">140.16</Weight>
-<Weight type="physical">140.071154</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0015">
-<Formula>C 2 H 2 N 0 O 1</Formula>
-<Weight type="chemical">42.04</Weight>
-<Weight type="physical">42.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sielecki, A.R.</Author>
-<Author>James, M.N.G.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, May 1990</Citation>
-<Description>Structures of product and inhibitor complexes of Streptomyces griseus protease A at 1.8 A resolution. A model for serine protease catalysis.</Description>
-<Xref>PDB:3SGA</Xref>
-<Note>X-ray diffraction, 1.8 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lim, W.A.</Author>
-<Author>Richards, F.M.</Author>
-<Author>Fox, R.O.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, March 1995</Citation>
-<Description>Structural determinants of peptide-binding orientation and of sequence specificity in SH3 domains.</Description>
-<Xref>PDB:1SEM</Xref>
-<Note>X-ray diffraction, 2.0 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Houtz, R.L.</Author>
-<Author>Stults, J.T.</Author>
-<Author>Mulligan, R.M.</Author>
-<Author>Tolbert, N.E.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 86, 1855-1859, 1989</Citation>
-<Title>Post-translational modifications in the large subunit of ribulose bisphosphate carboxylase/oxygenase.</Title>
-<Xref>DOI:10.1073/pnas.86.6.1855</Xref>
-<Xref>PMID:2928307</Xref>
-<Note>mass spectrometric identification</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>P</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0017197</Xref>
-<Xref>PSI-MOD:00059</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>acetylated amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n-acetylproline__p">MOD_RES N-acetylproline</Feature>
-</Features>
-<Image src="/images/AA0050.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0050.PDB" />
-</Entry>
-<Entry id="AA0051">
-<Header>
-<Code>AA0051</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-acetyl-L-serine</Name>
-<AlternateName>2-acetylamino-3-hydroxypropanoic acid</AlternateName>
-<AlternateName>2-acetylazanyl-3-hydroxypropanoic acid</AlternateName>
-<AlternateName>N-acetylserine</AlternateName>
-<SystematicName>(2S)-2-acetamido-3-hydroxypropanoic acid</SystematicName>
-<Xref>CAS:16354-58-8</Xref>
-<Xref>ChEBI:45441</Xref>
-<Xref>PDBHET:ACE</Xref>
-<Xref>PDBHET:SAC</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 8 N 1 O 3</Formula>
-<Weight type="chemical">130.12</Weight>
-<Weight type="physical">130.050418</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 2 H 2 N 0 O 1</Formula>
-<Weight type="chemical">42.04</Weight>
-<Weight type="physical">42.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Strickland, W.N.</Author>
-<Author>Strickland, M.S.</Author>
-<Author>de Groot, P.C.</Author>
-<Author>von Holt, C.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 109, 151-158, 1980</Citation>
-<Title>The primary structure of histone H2A from the sperm cell of the sea urchin Parechinus angulosus.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1980.tb04779.x</Xref>
-<Xref>PMID:6997045</Xref>
-<Note>N-acetylserine converted by N-&gt;O acyl shift to remove blockage</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wellner, D.</Author>
-<Author>Panneerselvam, C.</Author>
-<Author>Horecker, B.L.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 87, 1947-1949, 1990</Citation>
-<Title>Sequencing of peptides and proteins with blocked N-terminal amino acids: N-acetylserine or N-acetylthreonine.</Title>
-<Xref>DOI:10.1073/pnas.87.5.1947</Xref>
-<Xref>PMID:2106685</Xref>
-<Note>N-acetylserine converted by N-&gt;O acyl shift to remove blockage</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Declercq, J.P.</Author>
-<Author>Tinant, B.</Author>
-<Author>Parello, J.</Author>
-<Author>Rambaud, J.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 220, 1017-1039, 1991</Citation>
-<Title>Ionic interactions with parvalbumins: crystal structure determination of pike 4.10 parvalbumin in four different ionic environments.</Title>
-<Xref>DOI:10.1016/0022-2836(91)90369-H</Xref>
-<Xref>PMID:1880797</Xref>
-<Note>X-ray diffraction, 1.65 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Declercq, J.P.</Author>
-<Author>Tinant, B.</Author>
-<Author>Parello, J.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, January 1995</Citation>
-<Description>X-ray structure of a new crystal form of pike 4.10 beta parvalbumin.</Description>
-<Xref>PDB:1PVB</Xref>
-<Note>X-ray diffraction, 1.75 angstroms</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>N-terminal amino-acid Nα-acetyltransferase NatA</EnzymeName>
-<EnzymeName>acetyl-CoA:N-terminal-Gly/Ala/Ser/Val/Cys/Thr-[protein] Nα-acetyltransferase (EC 2.3.1.256)</EnzymeName>
-<EnzymeName>N-terminal L-serine Nα-acetyltransferase NatD</EnzymeName>
-<EnzymeName>acetyl-CoA:N-terminal-L-seryl-[histone 4/2A] L-serine Nα-acetyltransferase (EC 2.3.1.257)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0017198</Xref>
-<Xref>PSI-MOD:00060</Xref>
-<Xref>PSI-MOD:00648</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>acetylated amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n-acetylserine__s">MOD_RES N-acetylserine</Feature>
-</Features>
-<Image src="/images/AA0051.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0051.PDB" />
-</Entry>
-<Entry id="AA0052">
-<Header>
-<Code>AA0052</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-acetyl-L-threonine</Name>
-<AlternateName>2-acetylamino-3-hydroxybutanoic acid</AlternateName>
-<AlternateName>2-acetylazanyl-3-hydroxybutanoic acid</AlternateName>
-<AlternateName>N-acetylthreonine</AlternateName>
-<AlternateName>N-methylcarbonylthreonine</AlternateName>
-<SystematicName>(2S,3R)-2-acetamido-3-hydroxybutanoic acid</SystematicName>
-<Xref>CAS:17093-74-2</Xref>
-<Xref>ChEBI:45826</Xref>
-<Xref>PDBHET:ACE</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 10 N 1 O 3</Formula>
-<Weight type="chemical">144.15</Weight>
-<Weight type="physical">144.066068</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0017">
-<Formula>C 2 H 2 N 0 O 1</Formula>
-<Weight type="chemical">42.04</Weight>
-<Weight type="physical">42.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Strickland, W.N.</Author>
-<Author>Strickland, M.S.</Author>
-<Author>de Groot, P.C.</Author>
-<Author>von Holt, C.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 109, 151-158, 1980</Citation>
-<Title>The primary structure of histone H2A from the sperm cell of the sea urchin Parechinus angulosus.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1980.tb04779.x</Xref>
-<Xref>PMID:6997045</Xref>
-<Note>N-acetylthreonine converted by N-&gt;O acyl shift to remove blockage</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wellner, D.</Author>
-<Author>Panneerselvam, C.</Author>
-<Author>Horecker, B.L.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 87, 1947-1949, 1990</Citation>
-<Title>Sequencing of peptides and proteins with blocked N-terminal amino acids: N-acetylserine or N-acetylthreonine.</Title>
-<Xref>DOI:10.1073/pnas.87.5.1947</Xref>
-<Xref>PMID:2106685</Xref>
-<Note>N-acetylthreonine converted by N-&gt;O acyl shift to remove blockage</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>N-terminal amino-acid Nα-acetyltransferase NatA</EnzymeName>
-<EnzymeName>acetyl-CoA:N-terminal-Gly/Ala/Ser/Val/Cys/Thr-[protein] Nα-acetyltransferase (EC 2.3.1.256)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>T</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0017199</Xref>
-<Xref>PSI-MOD:00061</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>acetylated amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n-acetylthreonine__t">MOD_RES N-acetylthreonine</Feature>
-</Features>
-<Image src="/images/AA0052.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0052.PDB" />
-</Entry>
-<Entry id="AA0053">
-<Header>
-<Code>AA0053</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-acetyl-L-tyrosine</Name>
-<AlternateName>2-acetylamino-3-(4-hydoxyphenyl)propanoic acid</AlternateName>
-<AlternateName>2-acetylazanyl-3-(4-hydoxyphenyl)propanoic acid</AlternateName>
-<AlternateName>N-acetyltyrosine</AlternateName>
-<SystematicName>(2S)-2-acetamido-3-(4-hydoxyphenyl)propanoic acid</SystematicName>
-<Xref>CAS:537-55-3</Xref>
-<Xref>ChEBI:21563</Xref>
-<Xref>PDBHET:ACE</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 11 H 12 N 1 O 3</Formula>
-<Weight type="chemical">206.22</Weight>
-<Weight type="physical">206.081718</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0019">
-<Formula>C 2 H 2 N 0 O 1</Formula>
-<Weight type="chemical">42.04</Weight>
-<Weight type="physical">42.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Smyth, D.G.</Author>
-<Author>Massey, D.E.</Author>
-<Author>Zakarian, S.</Author>
-<Author>Finnie, M.D.</Author>
-</Authors>
-<Citation>Nature 279, 252-254, 1979</Citation>
-<Title>Endorphins are stored in biologically active and inactive forms: isolation of alpha-N-acetyl peptides.</Title>
-<Xref>DOI:10.1038/279252a0</Xref>
-<Xref>PMID:440436</Xref>
-<Note>mass spectrometric identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kawauchi, H.</Author>
-<Author>Tubokawa, M.</Author>
-<Author>Muramoto, K.</Author>
-</Authors>
-<Citation>Biochem. Biophys. Res. Commun. 88, 1249-1254, 1979</Citation>
-<Title>Isolation and primary structure of endorphin from salmon pituitary glands.</Title>
-<Xref>DOI:10.1016/0006-291X(79)91114-8</Xref>
-<Xref>PMID:475783</Xref>
-<Note>chromatographic identification of N-acetyl-O5'-dansyl-tyrosine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lee, M.S.</Author>
-<Author>Gippert, G.P.</Author>
-<Author>Soman, K.V.</Author>
-<Author>Case, D.A.</Author>
-<Author>Wright, P.E.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, September 1989</Citation>
-<Description>Three-dimensional solution structure of a single zinc finger DNA-binding domain.</Description>
-<Xref>PDB:1ZNF</Xref>
-<Note>synthetic peptide; conformation by (1)H-NMR</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lee, M.S.</Author>
-<Author>Cavanagh, J.</Author>
-<Author>Wright, P.E.</Author>
-</Authors>
-<Citation>FEBS Lett. 254, 159-164, 1989</Citation>
-<Title>Complete assignment of the (1)H NMR spectrum of a synthetic zinc finger from Xfin. Sequential resonance assignments and secondary structure.</Title>
-<Xref>DOI:10.1016/0014-5793(89)81030-0</Xref>
-<Xref>PMID:2506074</Xref>
-<Note>(1)H-NMR characterization, synthetic peptide</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Tong, L.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, November 1995</Citation>
-<Description>Human P56-Lck tyrosine kinase SH2 Domain in complex with the phosphotyrosyl peptide Ac-PTyr-Glu-Glu-Ile (PYEEI peptide).</Description>
-<Xref>PDB:1LKK</Xref>
-<Note>X-ray diffraction, 1.0 angstroms, synthetic peptide</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>Y</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0018000</Xref>
-<Xref>PSI-MOD:00062</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>acetylated amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n-acetyltyrosine__y">MOD_RES N-acetyltyrosine</Feature>
-</Features>
-<Image src="/images/AA0053.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0053.PDB" />
-</Entry>
-<Entry id="AA0054">
-<Header>
-<Code>AA0054</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-acetyl-L-valine</Name>
-<AlternateName>2-acetylamino-3-methylbutanoic acid</AlternateName>
-<AlternateName>2-acetylazanyl-3-methylbutanoic acid</AlternateName>
-<AlternateName>N-acetylvaline</AlternateName>
-<SystematicName>(2S)-2-acetamido-3-methylbutanoic acid</SystematicName>
-<Xref>CAS:96-81-1</Xref>
-<Xref>ChEBI:21565</Xref>
-<Xref>PDBHET:ACE</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 12 N 1 O 2</Formula>
-<Weight type="chemical">142.18</Weight>
-<Weight type="physical">142.086804</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0020">
-<Formula>C 2 H 2 N 0 O 1</Formula>
-<Weight type="chemical">42.04</Weight>
-<Weight type="physical">42.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Medzihradszky, K.F.</Author>
-<Author>Gibson, B.W.</Author>
-<Author>Kaur, S.</Author>
-<Author>Yu, Z.H.</Author>
-<Author>Medzihradszky, D.</Author>
-<Author>Burlingame, A.L.</Author>
-<Author>Bass, N.M.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 203, 327-339, 1992</Citation>
-<Title>The primary structure of fatty-acid-binding protein from nurse shark liver. Structural and evolutionary relationship to the mammalian fatty-acid-binding protein family.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1992.tb16553.x</Xref>
-<Xref>PMID:1735421</Xref>
-<Note>mass spectrometric identification</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>N-terminal amino-acid Nα-acetyltransferase NatA</EnzymeName>
-<EnzymeName>acetyl-CoA:N-terminal-Gly/Ala/Ser/Val/Cys/Thr-[protein] Nα-acetyltransferase (EC 2.3.1.256)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>V</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0018001</Xref>
-<Xref>PSI-MOD:00063</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>acetylated amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n-acetylvaline__v">MOD_RES N-acetylvaline</Feature>
-</Features>
-<Image src="/images/AA0054.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0054.PDB" />
-</Entry>
-<Entry id="AA0055">
-<Header>
-<Code>AA0055</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6-acetyl-L-lysine</Name>
-<AlternateName>6-acetylamino-2-aminohexanoic acid</AlternateName>
-<AlternateName>6-acetylazanyl-2-aminohexanoic acid</AlternateName>
-<AlternateName>epsilon-acetyllysine</AlternateName>
-<AlternateName>N(zeta)-acetyllysine</AlternateName>
-<SystematicName>(2S)-6-acetamido-2-aminohexanoic acid</SystematicName>
-<Xref>CAS:692-04-6</Xref>
-<Xref>ChEBI:61930</Xref>
-<Xref>PDBHET:ALY</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 8 H 14 N 2 O 2</Formula>
-<Weight type="chemical">170.21</Weight>
-<Weight type="physical">170.105528</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 2 H 2 N 0 O 1</Formula>
-<Weight type="chemical">42.04</Weight>
-<Weight type="physical">42.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hase, T.</Author>
-<Author>Wakabayashi, S.</Author>
-<Author>Matsubara, H.</Author>
-<Author>Kerscher, L.</Author>
-<Author>Oesterhelt, D.</Author>
-<Author>Rao, K.K.</Author>
-<Author>Hall, D.O.</Author>
-</Authors>
-<Citation>J. Biochem. 83, 1657-1670, 1978</Citation>
-<Title>Complete amino acid sequence of Halobacterium halobium ferredoxin containing an N(epsilon)-acetyllysine residue.</Title>
-<Xref>PMID:670159</Xref>
-<Note>chemical synthesis; chromatographic detection</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Edde, B.</Author>
-<Author>Rossier, J.</Author>
-<Author>Le Caer, J.P.</Author>
-<Author>Berwald-Netter, Y.</Author>
-<Author>Koulakoff, A.</Author>
-<Author>Gros, F.</Author>
-<Author>Denoulet, P.</Author>
-</Authors>
-<Citation>J. Cell. Biochem. 46, 134-142, 1991</Citation>
-<Title>A combination of posttranslational modifications is responsible for the production of neuronal alpha-tubulin heterogeneity.</Title>
-<Xref>DOI:10.1002/jcb.240460207</Xref>
-<Xref>PMID:1680872</Xref>
-<Note>chromatographic detection and radioisotope labeling</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Frolow, F.</Author>
-<Author>Harel, M.</Author>
-<Author>Sussman, J.L.</Author>
-<Author>Shoham, M.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, April 1996</Citation>
-<Description>2Fe-2S Ferredoxin from Haloarcula marismortui.</Description>
-<Xref>PDB:1DOI</Xref>
-<Note>X-ray diffraction, 1.9 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lapko, V.N.</Author>
-<Author>Smith, D.L.</Author>
-<Author>Smith, J.B.</Author>
-</Authors>
-<Citation>Protein Sci. 10, 1130-1136, 2001</Citation>
-<Title>In vivo carbamylation and acetylation of water-soluble human lens alphaB-crystallin lysine 92.</Title>
-<Xref>DOI:10.1110/ps.40901</Xref>
-<Xref>PMID:11369851</Xref>
-<Note>mass spectrometric detection with N6-carboxy-L-lysine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hirota, J.</Author>
-<Author>Satomi, Y.</Author>
-<Author>Yoshikawa, K.</Author>
-<Author>Takao, T.</Author>
-</Authors>
-<Citation>Rapid Commun. Mass Spectrom. 17, 371-376, 2003</Citation>
-<Title>Epsilon-N,N,N-trimethyllysine-specific ions in matrix-assisted laser desorption/ionization-tandem mass spectrometry.</Title>
-<Xref>DOI:10.1002/rcm.924</Xref>
-<Xref>PMID:12590383</Xref>
-<Note>attempts to distinguish from nominally isobaric N6,N6,N6-trimethyllysine (see RESID:AA0074)</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>histone acetyltransferase (EC 2.3.1.48)</EnzymeName>
-<EnzymeName>tubulin N-acetyltransferase (EC 2.3.1.108)</EnzymeName>
-<EnzymeName>protein lysine N6-acetyltransferase (EC 2.3.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>GO:0018003</Xref>
-<Xref>PSI-MOD:00064</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>acetyllysine</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n6-acetyllysine__k">MOD_RES N6-acetyllysine</Feature>
-</Features>
-<Image src="/images/AA0055.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0055.PDB" />
-</Entry>
-<Entry id="AA0056">
-<Header>
-<Code>AA0056</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>13-Sep-2013</StrucRevDate>
-<TextChngDate>13-Sep-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-acetyl-L-cysteine</Name>
-<AlternateName>2-amino-3-(acetylthio)propanoic acid</AlternateName>
-<AlternateName>2-azanyl-3-(acetylsulfanyl)propanoic acid</AlternateName>
-<AlternateName>cysteine acetate thioester</AlternateName>
-<AlternateName>S-acetylcysteine</AlternateName>
-<SystematicName>(2R)-3-acetylsulfanyl-2-aminopropanoic acid</SystematicName>
-<Xref>CAS:15312-11-5</Xref>
-<Xref>PDBHET:SCY</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 7 N 1 O 2 S 1</Formula>
-<Weight type="chemical">145.18</Weight>
-<Weight type="physical">145.019749</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 2 H 2 N 0 O 1 S 0</Formula>
-<Weight type="chemical">42.04</Weight>
-<Weight type="physical">42.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wagner, A.F.V.</Author>
-<Author>Frey, M.</Author>
-<Author>Neugebauer, F.A.</Author>
-<Author>Schäfer, D.</Author>
-<Author>Knappe, J.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 89, 996-1000, 1992</Citation>
-<Title>The free radical in pyruvate formate-lyase is located on glycine-734.</Title>
-<Xref>DOI:10.1073/pnas.89.3.996</Xref>
-<Xref>PMID:1310545</Xref>
-<Note>evidence for an S-acetylcysteine intermediate</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>GO:0018219</Xref>
-<Xref>GO:0018326</Xref>
-<Xref>PSI-MOD:00065</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>thioester bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="act_site__s-acetylcysteine intermediate__c">ACT_SITE S-acetylcysteine intermediate</Feature>
-</Features>
-<Image src="/images/AA0056.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0056.PDB" />
-</Entry>
-<Entry id="AA0057">
-<Header>
-<Code>AA0057</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-formylglycine</Name>
-<AlternateName>(formylamino)acetic acid</AlternateName>
-<AlternateName>(formylazanyl)ethanoic acid</AlternateName>
-<AlternateName>2-formamidoacetic acid</AlternateName>
-<AlternateName>2-formamidoethanoic acid</AlternateName>
-<AlternateName>N(alpha)-formylglycine</AlternateName>
-<SystematicName>(formylamino)ethanoic acid</SystematicName>
-<Xref>CAS:2491-15-8</Xref>
-<Xref>ChEBI:21717</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 4 N 1 O 2</Formula>
-<Weight type="chemical">86.07</Weight>
-<Weight type="physical">86.024203</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0008">
-<Formula>C 1 H 0 N 0 O 1</Formula>
-<Weight type="chemical">28.01</Weight>
-<Weight type="physical">27.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lübke, K.</Author>
-<Author>Matthes, S.</Author>
-<Author>Kloss, G.</Author>
-</Authors>
-<Citation>Experientia 27, 765-767, 1971</Citation>
-<Title>Isolation and structure of N(α)-formyl melittin.</Title>
-<Xref>DOI:10.1007/BF02136852</Xref>
-<Xref>PMID:5139483</Xref>
-<Note>blocked N-terminal, apparent mass spectrometric and gas chromatographic detection; a typographic error in the title of the PubMed citation is corrected</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Dianoux, A.C.</Author>
-<Author>Tsugita, A.</Author>
-<Author>Przybylski, M.</Author>
-</Authors>
-<Citation>FEBS Lett. 174, 151-156, 1984</Citation>
-<Title>Mass spectral identification of the blocked N-terminal tryptic peptide of the ATPase inhibitor from beef heart mitochondria.</Title>
-<Xref>PMID:6236102</Xref>
-<Note>bovine mitochondrial ATPase inhibitor peptide with N-formylglycine supposedly identified by mass-spectrometry</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Runswick, M.J.</Author>
-<Author>Walker, J.E.</Author>
-<Author>Gibson, B.W.</Author>
-<Author>Williams, D.H.</Author>
-</Authors>
-<Citation>Biochem. J. 235, 515-519, 1986</Citation>
-<Title>The frayed N-terminal of the inhibitor protein of bovine mitochondrial F1-ATPase.</Title>
-<Xref>PMID:2874795</Xref>
-<Note>failure to confirm the presence of N-formylglycine in bovine mitochondrial ATPase inhibitor peptide</Note>
-</ReferenceBlock>
-<Comment>This modification should not be confused with L-3-oxoalanine, also referred to as C(alpha)-formylglycine (see RESID:AA0185).</Comment>
-<SequenceCode>
-<SequenceSpec>G</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0018005</Xref>
-<Xref>PSI-MOD:00066</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-<Keyword>formylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n-formylglycine__g">MOD_RES N-formylglycine</Feature>
-</Features>
-<Image src="/images/AA0057.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0057.PDB" />
-</Entry>
-<Entry id="AA0058">
-<Header>
-<Code>AA0058</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-2001</StrucRevDate>
-<TextChngDate>25-Feb-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-D-glucuronoyl-glycine</Name>
-<AlternateName>N-D-glucuronyl-glycine</AlternateName>
-<SystematicName>2-(glucuronoylamino)ethanoic acid</SystematicName>
-<Xref>CAS:62532-50-7</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 8 H 12 N 1 O 7</Formula>
-<Weight type="chemical">234.18</Weight>
-<Weight type="physical">234.061377</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0008">
-<Formula>C 6 H 8 N 0 O 6</Formula>
-<Weight type="chemical">176.12</Weight>
-<Weight type="physical">176.032088</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lin, T.S.</Author>
-<Author>Kolattukudy, P.E.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 106, 341-351, 1980</Citation>
-<Title>Structural studies on cutinase, a glycoprotein containing novel amino acids and glucuronic acid amide at the N terminus.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1980.tb04580.x</Xref>
-<Xref>PMID:7398618</Xref>
-<Note>chromatographic detection; chemical and spectrographic characterization; demonstration of amide linkage</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kolattukudy, P.E.</Author>
-</Authors>
-<Citation>Meth. Enzymol. 106, 210-217, 1984</Citation>
-<Title>Detection of an N-terminal glucuronamide linkage in proteins.</Title>
-<Xref>DOI:10.1016/0076-6879(84)06022-5</Xref>
-<Xref>PMID:6493057</Xref>
-<Note>chemical characterization</Note>
-</ReferenceBlock>
-<Comment>The glucuronic acid is linked as an amide, rather than as a glycoside (see RESID:AA0291). The alpha glucuronoyl form is shown.</Comment>
-<SequenceCode>
-<SequenceSpec>G</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0018007</Xref>
-<Xref>PSI-MOD:00067</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n-d-glucuronoyl glycine__g">MOD_RES N-D-glucuronoyl glycine</Feature>
-</Features>
-<Image src="/images/AA0058.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0058.PDB" />
-</Entry>
-<Entry id="AA0059">
-<Header>
-<Code>AA0059</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-2001</StrucRevDate>
-<TextChngDate>31-May-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-myristoyl-glycine</Name>
-<AlternateName>N-(1-oxotetradecyl)glycine</AlternateName>
-<AlternateName>N-myristylglycine</AlternateName>
-<AlternateName>N-tetradecanoylglycine</AlternateName>
-<SystematicName>(tetradecanoylamino)ethanoic acid</SystematicName>
-<Xref>CAS:14246-55-0</Xref>
-<Xref>PDBHET:MYR</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 16 H 30 N 1 O 2 +</Formula>
-<Weight type="chemical">268.42 +</Weight>
-<Weight type="physical">268.227654 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0008">
-<Formula>C 14 H 26 N 0 O 1 +</Formula>
-<Weight type="chemical">210.36 +</Weight>
-<Weight type="physical">210.198365 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ozols, J.</Author>
-<Author>Carr, S.A.</Author>
-<Author>Strittmatter, P.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 259, 13349-13354, 1984</Citation>
-<Title>Identification of the NH2-terminal blocking group of NADH-cytochrome b5 reductase as myristic acid and the complete amino acid sequence of the membrane-binding domain.</Title>
-<Xref>PMID:6436247</Xref>
-<Note>GC and FAB mass spectrometric characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Dizhoor, A.M.</Author>
-<Author>Ericsson, L.H.</Author>
-<Author>Johnson, R.S.</Author>
-<Author>Kumar, S.</Author>
-<Author>Olshevskaya, E.</Author>
-<Author>Zozulya, S.</Author>
-<Author>Neubert, T.A.</Author>
-<Author>Stryer, L.</Author>
-<Author>Hurley, J.B.</Author>
-<Author>Walsh, K.A.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 267, 16033-16036, 1992</Citation>
-<Title>The NH-2 terminus of retinal recoverin is acylated by a small family of fatty acids.</Title>
-<Xref>PMID:1386601</Xref>
-<Note>mass spectrometric characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Neubert, T.A.</Author>
-<Author>Johnson, R.S.</Author>
-<Author>Hurley, J.B.</Author>
-<Author>Walsh, K.A.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 267, 18274-18277, 1992</Citation>
-<Title>The rod transducin alpha subunit amino terminus is heterogeneously fatty acylated.</Title>
-<Xref>PMID:1326520</Xref>
-<Note>mass spectrometric and chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Griffith, J.P.</Author>
-<Author>Kim, J.L.</Author>
-<Author>Kim, E.E.</Author>
-<Author>Sintchak, M.D.</Author>
-<Author>Thomson, J.A.</Author>
-<Author>Fitzgibbon, M.J.</Author>
-<Author>Fleming, M.A.</Author>
-<Author>Caron, P.R.</Author>
-<Author>Hsiao, K.</Author>
-<Author>Navia, M.A.</Author>
-</Authors>
-<Citation>Cell 82, 507-522, 1995</Citation>
-<Title>X-ray structure of calcineurin inhibited by the immunophilin-immunosuppressant FKBP12-FK506 complex.</Title>
-<Xref>DOI:10.1016/0092-8674(95)90439-5</Xref>
-<Xref>PMID:7543369</Xref>
-<Note>X-ray diffraction, 2.5 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Griffith, J.P.</Author>
-<Author>Kim, J.L.</Author>
-<Author>Kim, E.E.</Author>
-<Author>Sintchak, M.D.</Author>
-<Author>Thomson, J.A.</Author>
-<Author>Fitzgibbon, M.J.</Author>
-<Author>Fleming, M.A.</Author>
-<Author>Caron, P.R.</Author>
-<Author>Hsiao, K.</Author>
-<Author>Navia, M.A.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, August 1996</Citation>
-<Description>Ternary complex of a calcineurin A fragment, calcineurin B, Fkbp12 and the immunosuppressant drug FK506 (tacrolimus).</Description>
-<Xref>PDB:1TCO</Xref>
-<Note>X-ray diffraction, 2.5 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Maurer-Stroh, S.</Author>
-<Author>Eisenhaber, B.</Author>
-<Author>Eisenhaber, F.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 317, 523-540, 2002</Citation>
-<Title>N-terminal N-myristoylation of proteins: refinement of the sequence motif and its taxon-specific differences.</Title>
-<Xref>DOI:10.1006/jmbi.2002.5425</Xref>
-<Xref>PMID:11955007</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Maurer-Stroh, S.</Author>
-<Author>Eisenhaber, B.</Author>
-<Author>Eisenhaber, F.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 317, 541-557, 2002</Citation>
-<Title>N-terminal N-myristoylation of proteins: prediction of substrate proteins from amino acid sequence.</Title>
-<Xref>DOI:10.1006/jmbi.2002.5426</Xref>
-<Xref>PMID:11955008</Xref>
-<Note>improved profile prediction for the modification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Vilas, G.L.</Author>
-<Author>Corvi, M.M.</Author>
-<Author>Plummer, G.J.</Author>
-<Author>Seime, A.M.</Author>
-<Author>Lambkin, G.R.</Author>
-<Author>Berthiaume, L.G.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 103, 6542-6547, 2006</Citation>
-<Title>Posttranslational myristoylation of caspase-activated p21-activated protein kinase 2 (PAK2) potentiates late apoptotic events.</Title>
-<Xref>DOI:10.1073/pnas.0600824103</Xref>
-<Xref>PMID:16617111</Xref>
-<Note>post-translational myristoylation of a proteolytically produced N-terminal glycine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Burnaevskiy, N.</Author>
-<Author>Fox, T.G.</Author>
-<Author>Plymire, D.A.</Author>
-<Author>Ertelt, J.M.</Author>
-<Author>Weigele, B.A.</Author>
-<Author>Selyunin, A.S.</Author>
-<Author>Way, S.S.</Author>
-<Author>Patrie, S.M.</Author>
-<Author>Alto, N.M.</Author>
-</Authors>
-<Citation>Nature 496, 106-109, 2013</Citation>
-<Title>Proteolytic elimination of N-myristoyl modifications by the Shigella virulence factor IpaJ.</Title>
-<Xref>DOI:10.1038/nature12004</Xref>
-<Xref>PMID:23535599</Xref>
-<Note>peptidase from an infective organism that removes N-myristoyl glycine</Note>
-</ReferenceBlock>
-<Comment>The myristyl group represents a mixture of saturated and unsaturated fatty acids. Depending on the membrane composition, fatty acids including C12:0, C14:0, C14:1, and C14:2 may be incorporated.</Comment>
-<Comment>This modification is usually co-translational, occurring as the protein N-terminal emerges from the ribosome and immediately after the initial methionine is cleaved. However, glycine myristoylation can in some cases be performed on an N-terminal glycine produced by a post-translational proteolytic cleavage.</Comment>
-<Comment>The ExPASy Prosite pattern PS00008 should only be used with extreme caution. Because that pattern is not anchored to an N-terminal glycine, it extravagantly overpredicts "myristoylation" sites throughout the entire length of many protein sequences. Glycine myristoylation can only occur once in any protein sequence - at the N-terminal.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>glycylpeptide N-tetradecanoyltransferase (EC 2.3.1.97)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>G</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0018008</Xref>
-<Xref>PSI-MOD:00068</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-<Keyword>lipoprotein</Keyword>
-<Keyword>myristoylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__n-myristoyl glycine__g">LIPID N-myristoyl glycine</Feature>
-</Features>
-<Image src="/images/AA0059.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0059.PDB" />
-</Entry>
-<Entry id="AA0060">
-<Header>
-<Code>AA0060</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-palmitoyl-L-cysteine</Name>
-<AlternateName>2-hexadecanamido-3-sulfanylpropanoic acid</AlternateName>
-<AlternateName>2-hexadecanoylamino-3-mercaptopropanoic acid</AlternateName>
-<AlternateName>N-(1-oxahexadecyl)-L-cysteine</AlternateName>
-<SystematicName>(2R)-2-hexadecanoylamino-3-sulfanylpropanoic acid</SystematicName>
-<Xref>CAS:67603-49-0</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 19 H 36 N 1 O 2 S 1 +</Formula>
-<Weight type="chemical">342.56 +</Weight>
-<Weight type="physical">342.246675 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 16 H 30 N 0 O 1 S 0 +</Formula>
-<Weight type="chemical">238.41 +</Weight>
-<Weight type="physical">238.229666 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hantke, K.</Author>
-<Author>Braun, V.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 34, 284-296, 1973</Citation>
-<Title>Covalent binding of lipid to protein.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1973.tb02757.x</Xref>
-<Xref>PMID:4575979</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bouchon, B.</Author>
-<Author>Klein, M.</Author>
-<Author>Bischoff, R.</Author>
-<Author>Van Dorsselaer, A.</Author>
-<Author>Roitsch, C.</Author>
-</Authors>
-<Citation>Anal. Biochem. 246, 52-61, 1997</Citation>
-<Title>Analysis of the lipidated recombinant outer surface protein A from Borrelia burgdorferi by mass spectrometry.</Title>
-<Xref>DOI:10.1006/abio.1996.9982</Xref>
-<Xref>PMID:9056182</Xref>
-<Note>mass spectrometric characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Pepinsky, R.B.</Author>
-<Author>Zeng, C.</Author>
-<Author>Wen, D.</Author>
-<Author>Rayhorn, P.</Author>
-<Author>Baker, D.P.</Author>
-<Author>Williams, K.P.</Author>
-<Author>Bixler, S.A.</Author>
-<Author>Ambrose, C.M.</Author>
-<Author>Garber, E.A.</Author>
-<Author>Miatkowski, K.</Author>
-<Author>Taylor, F.R.</Author>
-<Author>Wang, E.A.</Author>
-<Author>Galdes, A.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 273, 14037-14045, 1998</Citation>
-<Title>Identification of a palmitic acid-modified form of human Sonic hedgehog.</Title>
-<Xref>DOI:10.1074/jbc.273.22.14037</Xref>
-<Xref>PMID:9593755</Xref>
-<Note>chemical characterization and mutational analysis of the modified human protein in fly and other cell lines</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Le Henaff, M.</Author>
-<Author>Fontenelle, C.</Author>
-</Authors>
-<Citation>Arch. Microbiol. 173, 339-345, 2000</Citation>
-<Title>Chemical analysis of processing of spiralin, the major lipoprotein of Spiroplasma melliferum.</Title>
-<Xref>DOI:10.1007/s002030000145</Xref>
-<Xref>PMID:10896212</Xref>
-<Note>chemical characterization of N-palmitoyl cysteine and S-diacylated glyceryl cysteine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kulathila, R.</Author>
-<Author>Kulathila, R.</Author>
-<Author>Indic, M.</Author>
-<Author>van den Berg, B.</Author>
-</Authors>
-<Citation>PLoS One 6, e15610, 2011</Citation>
-<Title>Crystal structure of Escherichia coli CusC, the outer membrane component of a heavy metal efflux pump.</Title>
-<Xref>DOI:10.1371/journal.pone.0015610</Xref>
-<Xref>PMID:21249122</Xref>
-<Note>X-ray diffraction, 2.30 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>van den Berg, B.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, November 2010</Citation>
-<Description>Outer membrane protein cusC.</Description>
-<Xref>PDB:3PIK</Xref>
-<Note>X-ray diffraction, 2.30 angstroms</Note>
-</ReferenceBlock>
-<Comment>In bacteria, the enzyme producing this modification may use a mixture of saturated and unsaturated fatty acids and act in close association with the enzyme producing S-diacylglycerol-L-cysteine (see RESID:AA0107). The signal peptide that is cleaved immediately before the modified cysteine typically ends in the motif [ILMV]X[AGS]C.</Comment>
-<Comment>In eukaryotes, the enzyme acts in the absence of modification of the cysteine thiol and may proceed after initial S-acylation (see RESID:AA0106) through a cyclic intermediate to the final N-acyl form. The eukaryotic enzyme appears to act more efficiently following formation of a carboxyl-terminal cholesterol ester (see RESID:AA0309).</Comment>
-<Comment>This modification should not be confused with S-palmitoyl-cysteine (see RESID:AA0106).</Comment>
-<GeneratingEnzyme>
-<EnzymeName>protein S-acyltransferase</EnzymeName>
-<EnzymeName>palmitoyl-CoA:[protein]-L-cysteine S-palmitoyltransferase (EC 2.3.1.225)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Condition>incidental to RESID:AA0107</Condition>
-<Condition>incidental to RESID:AA0309</Condition>
-<Xref>GO:0018009</Xref>
-<Xref>PSI-MOD:00069</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-<Keyword>lipoprotein</Keyword>
-<Keyword>palmitoylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__n-palmitoyl cysteine__c">LIPID N-palmitoyl cysteine</Feature>
-</Features>
-<Image src="/images/AA0060.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0060.PDB" />
-</Entry>
-<Entry id="AA0061">
-<Header>
-<Code>AA0061</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-2001</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-methyl-L-alanine</Name>
-<AlternateName>2-methylazanylpropanoic acid</AlternateName>
-<AlternateName>N-methylalanine</AlternateName>
-<SystematicName>(2S)-2-methylaminopropanoic acid</SystematicName>
-<Xref>CAS:3913-67-5</Xref>
-<Xref>ChEBI:61922</Xref>
-<Xref>PDBHET:MAA</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 7 N 1 O 1</Formula>
-<Weight type="chemical">85.11</Weight>
-<Weight type="physical">85.052764</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0001">
-<Formula>C 1 H 2 N 0 O 0</Formula>
-<Weight type="chemical">14.03</Weight>
-<Weight type="physical">14.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Chen, R.</Author>
-<Author>Chen-Schmeisser, U.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 74, 4905-4908, 1977</Citation>
-<Title>Isopeptide linkage between N-alpha-monomethylalanine and lysine in ribosomal protein S11 from Escherichia coli.</Title>
-<Xref>DOI:10.1073/pnas.74.11.4905</Xref>
-<Xref>PMID:337304</Xref>
-<Note>isopeptide linkage erroneously reported because of preview</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Chen, R.</Author>
-<Author>Brosius, J.</Author>
-<Author>Wittmann-Liebold, B.</Author>
-<Author>Schäfer, W.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 111, 173-181, 1977</Citation>
-<Title>Occurrence of methylated amino acids as N-termini of proteins from Escherichia coli ribosomes.</Title>
-<Xref>DOI:10.1016/S0022-2836(77)80121-6</Xref>
-<Xref>PMID:323502</Xref>
-<Note>chemical characterization and synthesis; chromatographic and mass spectrometric identification; the omission of author "Schäfer, W." in the PubMed citation is corrected</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kamp, R.</Author>
-<Author>Wittmann-Liebold, B.</Author>
-</Authors>
-<Citation>FEBS Lett. 121, 117-122, 1980</Citation>
-<Title>Primary structure of protein S11 from Escherichia coli ribosomes.</Title>
-<Xref>DOI:10.1016/0014-5793(80)81278-6</Xref>
-<Xref>PMID:7007074</Xref>
-<Note>confirmation of monomethylation and premature cleavage during Edman coupling</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Janzen, C.J.</Author>
-<Author>Fernandez, J.P.</Author>
-<Author>Deng, H.</Author>
-<Author>Diaz, R.</Author>
-<Author>Hake, S.B.</Author>
-<Author>Cross, G.A.M.</Author>
-</Authors>
-<Citation>FEBS Lett. 580, 2306-2310, 2006</Citation>
-<Title>Unusual histone modifications in Trypanosoma brucei.</Title>
-<Xref>DOI:10.1016/j.febslet.2006.03.044</Xref>
-<Xref>PMID:16580668</Xref>
-<Note>mass-spectrometric identification of N-terminal N-methylalanine; the initials of G.A.M. Cross in the PubMed citation are corrected</Note>
-</ReferenceBlock>
-<Comment>Polypeptides with monomethylated amino terminals can undergo premature cleavage during the coupling step of an Edman degradation. This can result in "preview" with both a residue and the following residue being seen from the first step on through a sequence.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>N-terminal RCC1 methyltransferase</EnzymeName>
-<EnzymeName>protein N-terminal methyltransferase</EnzymeName>
-<EnzymeName>S-adenosyl-L-methionine:N-terminal-(A,P,S)PK-[protein] methyltransferase (EC 2.1.1.244)</EnzymeName>
-<EnzymeName>protein N-terminal monomethyltransferase</EnzymeName>
-<EnzymeName>S-adenosyl-L-methionine:N-terminal-(A,P,S)PK-[protein] monomethyltransferase (EC 2.1.1.299)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>A</SequenceSpec>
-<Xref>GO:0018011</Xref>
-<Xref>GO:0019716</Xref>
-<Xref>PSI-MOD:00070</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>methylated amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n-methylalanine__a">MOD_RES N-methylalanine</Feature>
-</Features>
-<Image src="/images/AA0061.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0061.PDB" />
-</Entry>
-<Entry id="AA0062">
-<Header>
-<Code>AA0062</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N,N,N-trimethyl-L-alanine</Name>
-<AlternateName>(1S)-1-carboxy-N,N,N-trimethylethanazanium</AlternateName>
-<AlternateName>(2S)-2-(trimethylammonio)propanoic acid</AlternateName>
-<AlternateName>N,N,N-trimethylalanine cation</AlternateName>
-<AlternateName>N,N,N-trimethylalaninium</AlternateName>
-<SystematicName>(1S)-1-carboxy-N,N,N-trimethylethanaminium</SystematicName>
-<Xref>CAS:44802-94-0</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 13 N 1 O 1</Formula>
-<FormalCharge>1+</FormalCharge>
-<Weight type="chemical">115.18</Weight>
-<Weight type="physical">115.099165</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0001">
-<Formula>C 3 H 7 N 0 O 0</Formula>
-<FormalCharge>1+</FormalCharge>
-<Weight type="chemical">43.09</Weight>
-<Weight type="physical">43.054227</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lederer, F.</Author>
-<Author>Alix, J.H.</Author>
-<Author>Hayes, D.</Author>
-</Authors>
-<Citation>Biochem. Biophys. Res. Commun. 77, 470-480, 1977</Citation>
-<Title>N-Trimethylalanine, a novel blocking group, found in E. coli ribosomal protein L11.</Title>
-<Xref>DOI:10.1016/S0006-291X(77)80004-1</Xref>
-<Xref>PMID:332162</Xref>
-<Note>radioisotope labeling; chromatographic and mass spectrographic identification; chemical synthesis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Dognin, M.J.</Author>
-<Author>Wittmann-Liebold, B.</Author>
-</Authors>
-<Citation>Hoppe-Seyler's Z. Physiol. Chem. 361, 1697-1705, 1980</Citation>
-<Title>Identification of methylated amino acids during sequence analysis. Application to the Escherichia coli ribosomal protein L11.</Title>
-<Xref>DOI:10.1515/bchm2.1980.361.2.1697</Xref>
-<Xref>PMID:6778808</Xref>
-<Note>chromatographic detection; mass spectrometric identification; chemical synthesis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Henry, G.D.</Author>
-<Author>Dalgarno, D.C.</Author>
-<Author>Levine, B.A.</Author>
-<Author>Trayer, I.P.</Author>
-</Authors>
-<Citation>Biochem. Soc. Trans. 10, 362-363, 1982</Citation>
-<Title>Discovery of alpha-N-trimethylalanine in myosin light chains and its role in actomyosin interaction.</Title>
-<Xref>DOI:10.1042/bst0100362</Xref>
-<Note>(1)H-NMR identification; chemical synthesis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Henry, G.D.</Author>
-<Author>Trayer, I.P.</Author>
-<Author>Brewer, S.</Author>
-<Author>Levine, B.A.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 148, 75-82, 1985</Citation>
-<Title>The widespread distribution of alpha-N-trimethylalanine as the N-terminal amino acid of light chains from vertebrate striated muscle myosins.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1985.tb08809.x</Xref>
-<Xref>PMID:3979397</Xref>
-<Note>mass spectrometric and (1)H-NMR detection</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Vanet, A.</Author>
-<Author>Plumbridge, J.A.</Author>
-<Author>Guerin, M.F.</Author>
-<Author>Alix, J.H.</Author>
-</Authors>
-<Citation>Mol. Microbiol. 14, 947-958, 1994</Citation>
-<Title>Ribosomal protein methylation in Escherichia coli: the gene prmA, encoding the ribosomal protein L11 methyltransferase, is dispensable.</Title>
-<Xref>DOI:10.1111/j.1365-2958.1994.tb01330.x</Xref>
-<Xref>PMID:7715456</Xref>
-</ReferenceBlock>
-<Comment>Consult FAQ at http://pir.georgetown.edu/resid/faq.shtml#q12 concerning calculation of the difference formula.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>ribosomal protein L11 methyltransferase prmA (EC 2.1.1.-)</EnzymeName>
-<EnzymeName>N-terminal RCC1 methyltransferase</EnzymeName>
-<EnzymeName>protein N-terminal methyltransferase</EnzymeName>
-<EnzymeName>S-adenosyl-L-methionine:N-terminal-(A,P,S)PK-[protein] methyltransferase (EC 2.1.1.244)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>A</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0018011</Xref>
-<Xref>GO:0018012</Xref>
-<Xref>PSI-MOD:00071</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-<Keyword>methylated amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n,n,n-trimethylalanine__a">MOD_RES N,N,N-trimethylalanine</Feature>
-</Features>
-<Image src="/images/AA0062.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0062.PDB" />
-</Entry>
-<Entry id="AA0063">
-<Header>
-<Code>AA0063</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-2001</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-methylglycine</Name>
-<AlternateName>L-sarcosine</AlternateName>
-<AlternateName>methylaminoacetic acid</AlternateName>
-<SystematicName>methylaminoethanoic acid</SystematicName>
-<Xref>CAS:107-97-1</Xref>
-<Xref>ChEBI:15611</Xref>
-<Xref>PDBHET:SAR</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 5 N 1 O 1</Formula>
-<Weight type="chemical">71.08</Weight>
-<Weight type="physical">71.037114</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0008">
-<Formula>C 1 H 2 N 0 O 0</Formula>
-<Weight type="chemical">14.03</Weight>
-<Weight type="physical">14.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kamitori, S.</Author>
-<Author>Takusagawa, F.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 225, 445-456, 1992</Citation>
-<Title>Crystal structure of the 2:1 complex between d(GAAGCTTC) and the anticancer drug actinomycin D.</Title>
-<Xref>DOI:10.1016/0022-2836(92)90931-9</Xref>
-<Xref>PMID:1593629</Xref>
-<Note>X-ray diffraction, 3.0 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bailey, A.O.</Author>
-<Author>Panchenko, T.</Author>
-<Author>Sathyan, K.M.</Author>
-<Author>Petkowski, J.J.</Author>
-<Author>Pai, P.J.</Author>
-<Author>Bai, D.L.</Author>
-<Author>Russell, D.H.</Author>
-<Author>Macara, I.G.</Author>
-<Author>Shabanowitz, J.</Author>
-<Author>Hunt, D.F.</Author>
-<Author>Black, B.E.</Author>
-<Author>Foltz, D.R.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 110, 11827-11832, 2013</Citation>
-<Title>Posttranslational modification of CENP-A influences the conformation of centromeric chromatin.</Title>
-<Xref>DOI:10.1073/pnas.1300325110</Xref>
-<Xref>PMID:23818633</Xref>
-<Note>mass spectrometric identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Dai, X.</Author>
-<Author>Otake, K.</Author>
-<Author>You, C.</Author>
-<Author>Cai, Q.</Author>
-<Author>Wang, Z.</Author>
-<Author>Masumoto, H.</Author>
-<Author>Wang, Y.</Author>
-</Authors>
-<Citation>J. Proteome Res. 12, 4167-4175, 2013</Citation>
-<Title>Identification of novel α-n-methylation of CENP-B that regulates its binding to the centromeric DNA.</Title>
-<Xref>DOI:10.1021/pr400498y</Xref>
-<Xref>PMID:23978223</Xref>
-<Note>mass spectrometric identification</Note>
-</ReferenceBlock>
-<Comment>Sarcosine occurs internally in some nonencoded peptides. It has been observed as a minor post-translational modification arising from the incomplete trimethylation of N-terminal glycine.  See RESID:AA0619 and RESID:AA0620.</Comment>
-<Comment>Polypeptides with monomethylated amino terminals can undergo premature cleavage during the coupling step of an Edman degradation. This can result in "preview" with both a residue and the following residue being seen from the first step on through a sequence.</Comment>
-<Comment>It is not clear whether the N-terminal methyltransferase responsible for methylating N-terminal glycine is distinguishable from the enzyme activities of EC 2.1.1.244 or EC 2.1.1.299.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>protein N-terminal methyltransferase (EC 2.1.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>G</SequenceSpec>
-<Xref>GO:0018013</Xref>
-<Xref>GO:0019736</Xref>
-<Xref>PSI-MOD:00072</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>methylated amino acid</Keyword>
-<Keyword>methylated amino end</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0063.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0063.PDB" />
-</Entry>
-<Entry id="AA0064">
-<Header>
-<Code>AA0064</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-2001</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-methyl-L-methionine</Name>
-<AlternateName>2-methylamino-4-(methylthio)butanoic acid</AlternateName>
-<AlternateName>N-methylmethionine</AlternateName>
-<SystematicName>(2S)-2-methylamino-4-(methylsulfanyl)butanoic acid</SystematicName>
-<Xref>CAS:42537-72-4</Xref>
-<Xref>ChEBI:61886</Xref>
-<Xref>PDBHET:MME</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 11 N 1 O 1 S 1</Formula>
-<Weight type="chemical">145.22</Weight>
-<Weight type="physical">145.056135</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0013">
-<Formula>C 1 H 2 N 0 O 0 S 0</Formula>
-<Weight type="chemical">14.03</Weight>
-<Weight type="physical">14.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Brosius, J.</Author>
-<Author>Chen, R.</Author>
-</Authors>
-<Citation>FEBS Lett. 68, 105-109, 1976</Citation>
-<Title>The primary structure of protein L16 located at the peptidyltransferase center of Escherichia coli ribosomes.</Title>
-<Xref>DOI:10.1016/0014-5793(76)80415-2</Xref>
-<Xref>PMID:786730</Xref>
-<Note>N-methylmethionine observed in Escherichia coli ribosomal protein L16</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Chen, R.</Author>
-<Author>Brosius, J.</Author>
-<Author>Wittmann-Liebold, B.</Author>
-<Author>Schäfer, W.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 111, 173-181, 1977</Citation>
-<Title>Occurrence of methylated amino acids as N-termini of proteins from Escherichia coli ribosomes.</Title>
-<Xref>DOI:10.1016/S0022-2836(77)80121-6</Xref>
-<Xref>DOI:10.1016/S0022-2836(77)80121-6</Xref>
-<Xref>PMID:323502</Xref>
-<Note>chemical characterization and synthesis; chromatographic and mass spectrometric identification; the omission of author "Schäfer, W." in the PubMed citation is corrected</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Stock, A.</Author>
-<Author>Schaeffer, E.</Author>
-<Author>Koshland Jr., D.E.</Author>
-<Author>Stock, J.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 262, 8011-8014, 1987</Citation>
-<Title>A second type of protein methylation reaction in bacterial chemotaxis.</Title>
-<Xref>PMID:3298225</Xref>
-<Note>radioisotope labeling; chromatographic detection of PTH derivative</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Forest, K.T.</Author>
-<Author>Dunham, S.A.</Author>
-<Author>Koomey, M.</Author>
-<Author>Tainer, J.A.</Author>
-</Authors>
-<Citation>Mol. Microbiol. 31, 743-752, 1999</Citation>
-<Title>Crystallographic structure reveals phosphorylated pilin from Neisseria: phosphoserine sites modify type IV pilus surface chemistry and fibre morphology.</Title>
-<Xref>DOI:10.1046/J.1365-2958.1999.01184.X</Xref>
-<Xref>PMID:10048019</Xref>
-<Note>X-ray diffraction, 2.60 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Forest, K.T.</Author>
-<Author>Dunham, S.A.</Author>
-<Author>Koomey, M.</Author>
-<Author>Tainer, J.A.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, March 1998</Citation>
-<Description>Crystallographic structure of phosphorylated pilin from Neisseria: phosphoserine sites modify type IV pilus surface chemistry.</Description>
-<Xref>PDB:1PIL</Xref>
-<Note>X-ray diffraction, 2.60 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Taylor, T.C.</Author>
-<Author>Backlund, A.</Author>
-<Author>Bjorhall, K.</Author>
-<Author>Spreitzer, R.J.</Author>
-<Author>Andersson, I.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 276, 48159-48164, 2001</Citation>
-<Title>First crystal structure of Rubisco from a green alga, Chlamydomonas reinhardtii.</Title>
-<Xref>DOI:10.1074/jbc.M107765200</Xref>
-<Xref>PMID:11641402</Xref>
-<Note>X-ray diffraction, 1.40 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Taylor, T.C.</Author>
-<Author>Spreitzer, R.J.</Author>
-<Author>Andersson, I.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, August 2001</Citation>
-<Description>Rubisco from Chlamydomonas reinhardtii.</Description>
-<Xref>PDB:1GK8</Xref>
-<Note>X-ray diffraction, 1.40 angstroms</Note>
-</ReferenceBlock>
-<Comment>Polypeptides with monomethylated amino terminals can undergo premature cleavage during the coupling step of an Edman degradation. This can result in "preview" with both a residue and the following residue being seen from the first step on through a sequence.</Comment>
-<Comment>Although appropriate, the keyword "thioether bond" normally does not appear for this amino acid.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>S-adenosylmethionine--methionyl-peptide N-methyltransferase (EC 2.1.1.-)</EnzymeName>
-<EnzymeName>prepilin peptidase (EC 3.4.23.43)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>M</SequenceSpec>
-<Xref>GO:0018014</Xref>
-<Xref>PSI-MOD:00073</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>*thioether bond</Keyword>
-<Keyword>methylated amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n-methylmethionine__m">MOD_RES N-methylmethionine</Feature>
-</Features>
-<Image src="/images/AA0064.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0064.PDB" />
-</Entry>
-<Entry id="AA0065">
-<Header>
-<Code>AA0065</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-2001</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-methyl-L-phenylalanine</Name>
-<AlternateName>N-methylphenylalanine</AlternateName>
-<SystematicName>(2S)-2-methylamino-3-phenylpropanoic acid</SystematicName>
-<Xref>CAS:2566-30-5</Xref>
-<Xref>ChEBI:61884</Xref>
-<Xref>PDBHET:MEA</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 10 H 11 N 1 O 1</Formula>
-<Weight type="chemical">161.20</Weight>
-<Weight type="physical">161.084064</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0014">
-<Formula>C 1 H 2 N 0 O 0</Formula>
-<Weight type="chemical">14.03</Weight>
-<Weight type="physical">14.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hermodson, M.A.</Author>
-<Author>Chen, K.C.S.</Author>
-<Author>Buchanan, T.M.</Author>
-</Authors>
-<Citation>Biochemistry 17, 442-445, 1978</Citation>
-<Title>Neisseria pili proteins: amino-terminal amino acid sequences and identification of an unusual amino acid.</Title>
-<Xref>DOI:10.1021/bi00596a010</Xref>
-<Xref>PMID:413571</Xref>
-<Note>chromatographic determination</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>McKern, N.M.</Author>
-<Author>Stewart, D.J.</Author>
-<Author>Strike, P.M.</Author>
-</Authors>
-<Citation>J. Protein Chem. 7, 157-164, 1988</Citation>
-<Title>Amino acid sequences of pilins from serologically distinct strains of Bacteroides nodosus.</Title>
-<Xref>DOI:10.1007/BF01025245</Xref>
-<Xref>PMID:2577730</Xref>
-<Note>chromatographic determination</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Strom, M.S.</Author>
-<Author>Lory, S.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 266, 1656-1664, 1991</Citation>
-<Title>Amino acid substitutions in pilin of Pseudomonas aeruginosa. Effect on leader peptide cleavage, amino-terminal methylation, and pilus assembly.</Title>
-<Xref>PMID:1671038</Xref>
-<Note>the amino-terminal methyltransferase activity of prepilin peptidase is not specific for phenylalanine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Forest, K.T.</Author>
-<Author>Dunham, S.A.</Author>
-<Author>Koomey, M.</Author>
-<Author>Tainer, J.A.</Author>
-</Authors>
-<Citation>Mol. Microbiol. 31, 743-752, 1999</Citation>
-<Title>Crystallographic structure reveals phosphorylated pilin from Neisseria: phosphoserine sites modify type IV pilus surface chemistry and fibre morphology.</Title>
-<Xref>DOI:10.1046/J.1365-2958.1999.01184.X</Xref>
-<Xref>PMID:10048019</Xref>
-<Note>X-ray diffraction, 2.60 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Forest, K.T.</Author>
-<Author>Dunham, S.A.</Author>
-<Author>Koomey, M.</Author>
-<Author>Tainer, J.A.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, March 1998</Citation>
-<Description>Crystallographic structure of phosphorylated pilin from Neisseria: phosphoserine sites modify type IV pilus surface chemistry.</Description>
-<Xref>PDB:1PIL</Xref>
-<Note>X-ray diffraction, 2.60 angstroms</Note>
-</ReferenceBlock>
-<Comment>Polypeptides with monomethylated amino terminals can undergo premature cleavage during the coupling step of an Edman degradation. This can result in "preview" with both a residue and the following residue being seen from the first step on through a sequence.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>prepilin peptidase (EC 3.4.23.43)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>F</SequenceSpec>
-<Xref>GO:0018015</Xref>
-<Xref>PSI-MOD:00074</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>methylated amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n-methylphenylalanine__f">MOD_RES N-methylphenylalanine</Feature>
-</Features>
-<Image src="/images/AA0065.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0065.PDB" />
-</Entry>
-<Entry id="AA0066">
-<Header>
-<Code>AA0066</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N,N-dimethyl-L-proline</Name>
-<AlternateName>1,1-dimethyl-L-prolinium</AlternateName>
-<AlternateName>N,N-dimethyl-L-prolinium</AlternateName>
-<AlternateName>stachydrin</AlternateName>
-<SystematicName>(2S)-2-carboxy-1,1-dimethylpyrrolidinium</SystematicName>
-<Xref>CAS:51705-67-0</Xref>
-<Xref>ChEBI:21451</Xref>
-<Xref>PDBHET:PBE</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 13 N 1 O 1</Formula>
-<FormalCharge>1+</FormalCharge>
-<Weight type="chemical">127.19</Weight>
-<Weight type="physical">127.099165</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0015">
-<Formula>C 2 H 5 N 0 O 0</Formula>
-<FormalCharge>1+</FormalCharge>
-<Weight type="chemical">29.06</Weight>
-<Weight type="physical">29.038577</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Pettigrew, G.W.</Author>
-<Author>Smith, G.M.</Author>
-</Authors>
-<Citation>Nature 265, 661-662, 1977</Citation>
-<Title>Novel N-terminal protein blocking group identified as dimethylproline.</Title>
-<Xref>DOI:10.1038/265661a0</Xref>
-<Xref>PMID:193025</Xref>
-<Note>(1)H-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Smith, G.M.</Author>
-<Author>Pettigrew, G.W.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 110, 123-130, 1980</Citation>
-<Title>Identification of N,N-dimethylproline as the N-terminal blocking group of Crithidia oncopelti cytochrome c557.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1980.tb04847.x</Xref>
-<Xref>PMID:6254758</Xref>
-<Note>chromatographic separation; mass spectrometric, (1)H-NMR and (13)C-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Martinage, A.</Author>
-<Author>Briand, G.</Author>
-<Author>Van Dorsselaer, A.</Author>
-<Author>Turner, C.H.</Author>
-<Author>Sautiere, P.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 147, 351-359, 1985</Citation>
-<Title>Primary structure of histone H2B from gonads of the starfish Asterias rubens. Identification of an N-dimethylproline residue at the amino-terminal.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1985.tb08757.x</Xref>
-<Xref>PMID:3882426</Xref>
-<Note>mass spectrometric and (1)H-NMR identification</Note>
-</ReferenceBlock>
-<Comment>Consult FAQ at http://pir.georgetown.edu/resid/faq.shtml#q12 concerning calculation of the difference formula.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>N-terminal RCC1 methyltransferase</EnzymeName>
-<EnzymeName>protein N-terminal methyltransferase</EnzymeName>
-<EnzymeName>S-adenosyl-L-methionine:N-terminal-(A,P,S)PK-[protein] methyltransferase (EC 2.1.1.244)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>P</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0018016</Xref>
-<Xref>GO:0035568</Xref>
-<Xref>PSI-MOD:00075</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-<Keyword>methylated amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n,n-dimethylproline__p">MOD_RES N,N-dimethylproline</Feature>
-</Features>
-<Image src="/images/AA0066.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0066.PDB" />
-</Entry>
-<Entry id="AA0067">
-<Header>
-<Code>AA0067</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N(omega)-,N(omega')-dimethyl-L-arginine</Name>
-<AlternateName>N3,N4-dimethylarginine</AlternateName>
-<AlternateName>N5-[(methylamino)(methylimino)methyl]ornithine</AlternateName>
-<AlternateName>NG,N'G-dimethylarginine</AlternateName>
-<AlternateName>symmetric dimethylarginine</AlternateName>
-<SystematicName>(2S)-2-amino-5-[((methylamino)(methylimino)methyl)amino]pentanoic acid</SystematicName>
-<Xref>CAS:30344-00-4</Xref>
-<Xref>ChEBI:61916</Xref>
-<Xref>PDBHET:2MR</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 8 H 16 N 4 O 1</Formula>
-<Weight type="chemical">184.24</Weight>
-<Weight type="physical">184.132411</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0002">
-<Formula>C 2 H 4 N 0 O 0</Formula>
-<Weight type="chemical">28.05</Weight>
-<Weight type="physical">28.031300</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Baldwin, G.S.</Author>
-<Author>Carnegie, P.R.</Author>
-</Authors>
-<Citation>Biochem. J. 123, 69-74, 1971</Citation>
-<Title>Isolation and partial characterization of methylated arginines from the encephalitogenic basic protein of myelin.</Title>
-<Xref>PMID:5128665</Xref>
-<Note>chromatographic isolation; chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Scoble, H.A.</Author>
-<Author>Whitaker, J.N.</Author>
-<Author>Biemann, K.</Author>
-</Authors>
-<Citation>J. Neurochem. 47, 614-616, 1986</Citation>
-<Title>Analysis of the primary sequence of human myelin basic protein peptides 1-44 and 90-170 by fast atom bombardment mass spectrometry.</Title>
-<Xref>DOI:10.1111/j.1471-4159.1986.tb04544.x</Xref>
-<Xref>PMID:2426402</Xref>
-<Note>mass spectrometric analysis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Zou, Y.</Author>
-<Author>Wang, Y.</Author>
-</Authors>
-<Citation>Biochemistry 44, 6293-6301, 2005</Citation>
-<Title>Tandem mass spectrometry for the examination of the posttranslational modifications of high-mobility group A1 proteins: symmetric and asymmetric dimethylation of Arg25 in HMGA1a protein.</Title>
-<Xref>DOI:10.1021/bi0475525</Xref>
-<Xref>PMID:15835918</Xref>
-<Note>mass spectrometric differentiation between symmetric and asymmetric dimethylarginine by neutral loss fragments</Note>
-</ReferenceBlock>
-<Comment>This modification should not be confused with omega-N,omega-N-dimethyl-L-arginine (see RESID:AA0068) or N2,N2-dimethyl-L-arginine (see RESID:AA0569).</Comment>
-<GeneratingEnzyme>
-<EnzymeName>[myelin basic protein]-arginine N-methyltransferase (EC 2.1.1.126)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>R</SequenceSpec>
-<Xref>GO:0018216</Xref>
-<Xref>GO:0019918</Xref>
-<Xref>PSI-MOD:00076</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>methylated amino acid</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__symmetric dimethylarginine__r">MOD_RES Symmetric dimethylarginine</Feature>
-<Feature type="UniProt" key="mod_res__omega-n-methylated arginine__r">MOD_RES Omega-N-methylated arginine</Feature>
-</Features>
-<Image src="/images/AA0067.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0067.PDB" />
-</Entry>
-<Entry id="AA0068">
-<Header>
-<Code>AA0068</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N(omega)-,N(omega)-dimethyl-L-arginine</Name>
-<AlternateName>asymmetric dimethylarginine</AlternateName>
-<AlternateName>N5-[(dimethylamino)(imino)methyl]ornithine</AlternateName>
-<AlternateName>NG,NG-dimethylarginine</AlternateName>
-<SystematicName>(2S)-2-amino-5-([(dimethylamino)(imino)methyl]amino)pentanoic acid</SystematicName>
-<Xref>CAS:30315-93-6</Xref>
-<Xref>ChEBI:61896</Xref>
-<Xref>PDBHET:DA2</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 8 H 16 N 4 O 1</Formula>
-<Weight type="chemical">184.24</Weight>
-<Weight type="physical">184.132411</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0002">
-<Formula>C 2 H 4 N 0 O 0</Formula>
-<Weight type="chemical">28.05</Weight>
-<Weight type="physical">28.031300</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Merrill, B.M.</Author>
-<Author>Lopresti, M.B.</Author>
-<Author>Stone, K.L.</Author>
-<Author>Williams, K.R.</Author>
-</Authors>
-<Citation>Int. J. Pept. Protein Res. 29, 21-39, 1987</Citation>
-<Title>Amino acid sequence of UP1, an hnRNP-derived single-stranded nucleic acid binding protein from calf thymus.</Title>
-<Xref>PMID:3032834</Xref>
-<Note>chromatographic identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yague, J.</Author>
-<Author>Vazquez, J.</Author>
-<Author>Lopez de Castro, J.A.</Author>
-</Authors>
-<Citation>Protein Sci. 9, 2210-2217, 2000</Citation>
-<Title>A post-translational modification of nuclear proteins, N(G),N(G)-dimethyl-Arg, found in a natural HLA class I peptide ligand.</Title>
-<Xref>DOI:10.1110/ps.9.11.2210</Xref>
-<Xref>PMID:11152131</Xref>
-<Note>mass spectrometric detection</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Zou, Y.</Author>
-<Author>Wang, Y.</Author>
-</Authors>
-<Citation>Biochemistry 44, 6293-6301, 2005</Citation>
-<Title>Tandem mass spectrometry for the examination of the posttranslational modifications of high-mobility group A1 proteins: symmetric and asymmetric dimethylation of Arg25 in HMGA1a protein.</Title>
-<Xref>DOI:10.1021/bi0475525</Xref>
-<Xref>PMID:15835918</Xref>
-<Note>mass spectrometric differentiation between symmetric and asymmetric dimethylarginine by neutral loss fragments</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kuhn, P.</Author>
-<Author>Xu, Q.</Author>
-<Author>Cline, E.</Author>
-<Author>Zhang, D.</Author>
-<Author>Ge, Y.</Author>
-<Author>Xu, W.</Author>
-</Authors>
-<Citation>Protein Sci. 18, 1272-1280, 2009</Citation>
-<Title>Delineating Anopheles gambiae coactivator associated arginine methyltransferase 1 automethylation using top-down high resolution tandem mass spectrometry.</Title>
-<Xref>DOI:10.1002/pro.139</Xref>
-<Xref>PMID:19472346</Xref>
-<Note>mass spectrometric detection of an intermolecular autocatalytic modification</Note>
-</ReferenceBlock>
-<Comment>This modification should not be confused with omega-N,omega-N'-dimethyl-L-arginine (see RESID:AA0067) or N2,N2-dimethyl-L-arginine (see RESID:AA0569).</Comment>
-<GeneratingEnzyme>
-<EnzymeName>histone-arginine N-methyltransferase (EC 2.1.1.125)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>R</SequenceSpec>
-<Xref>GO:0018216</Xref>
-<Xref>GO:0019919</Xref>
-<Xref>PSI-MOD:00077</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>methylated amino acid</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__asymmetric dimethylarginine__r">MOD_RES Asymmetric dimethylarginine</Feature>
-<Feature type="UniProt" key="mod_res__omega-n-methylated arginine__r">MOD_RES Omega-N-methylated arginine</Feature>
-</Features>
-<Image src="/images/AA0068.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0068.PDB" />
-</Entry>
-<Entry id="AA0069">
-<Header>
-<Code>AA0069</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N(omega)-methyl-L-arginine</Name>
-<AlternateName>NG-methylarginine</AlternateName>
-<SystematicName>(2S)-2-amino-5-[(imino(methylamino)methyl)amino]pentanoic acid</SystematicName>
-<Xref>CAS:17035-90-4</Xref>
-<Xref>ChEBI:65309</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 14 N 4 O 1</Formula>
-<Weight type="chemical">170.22</Weight>
-<Weight type="physical">170.116761</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0002">
-<Formula>C 1 H 2 N 0 O 0</Formula>
-<Weight type="chemical">14.03</Weight>
-<Weight type="physical">14.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Baldwin, G.S.</Author>
-<Author>Carnegie, P.R.</Author>
-</Authors>
-<Citation>Biochem. J. 123, 69-74, 1971</Citation>
-<Title>Isolation and partial characterization of methylated arginines from the encephalitogenic basic protein of myelin.</Title>
-<Xref>PMID:5128665</Xref>
-<Note>chromatographic isolation; chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Scoble, H.A.</Author>
-<Author>Whitaker, J.N.</Author>
-<Author>Biemann, K.</Author>
-</Authors>
-<Citation>J. Neurochem. 47, 614-616, 1986</Citation>
-<Title>Analysis of the primary sequence of human myelin basic protein peptides 1-44 and 90-170 by fast atom bombardment mass spectrometry.</Title>
-<Xref>DOI:10.1111/j.1471-4159.1986.tb04544.x</Xref>
-<Xref>PMID:2426402</Xref>
-<Note>mass spectrometric analysis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Zou, Y.</Author>
-<Author>Wang, Y.</Author>
-</Authors>
-<Citation>Biochemistry 44, 6293-6301, 2005</Citation>
-<Title>Tandem mass spectrometry for the examination of the posttranslational modifications of high-mobility group A1 proteins: symmetric and asymmetric dimethylation of Arg25 in HMGA1a protein.</Title>
-<Xref>DOI:10.1021/bi0475525</Xref>
-<Xref>PMID:15835918</Xref>
-<Note>mass spectrometric differentiation between symmetric and asymmetric dimethylarginine by neutral loss fragments</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>histone-arginine N-methyltransferase (EC 2.1.1.125)</EnzymeName>
-<EnzymeName>[myelin basic protein]-arginine N-methyltransferase (EC 2.1.1.126)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>R</SequenceSpec>
-<Xref>GO:0018216</Xref>
-<Xref>GO:0019918</Xref>
-<Xref>GO:0019919</Xref>
-<Xref>PSI-MOD:00078</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>methylated amino acid</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__omega-n-methylarginine__r">MOD_RES Omega-N-methylarginine</Feature>
-<Feature type="UniProt" key="mod_res__omega-n-methylated arginine__r">MOD_RES Omega-N-methylated arginine</Feature>
-</Features>
-<Image src="/images/AA0069.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0069.PDB" />
-</Entry>
-<Entry id="AA0070">
-<Header>
-<Code>AA0070</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N4-methyl-L-asparagine</Name>
-<AlternateName>beta-aspartyl methylamide</AlternateName>
-<AlternateName>beta-methylasparagine [misnomer]</AlternateName>
-<AlternateName>N(gamma)-methylasparagine</AlternateName>
-<AlternateName>N-methylasparagine</AlternateName>
-<SystematicName>(2S)-2-amino-N4-methylbutanediamic acid</SystematicName>
-<Xref>CAS:7175-34-0</Xref>
-<Xref>ChEBI:61960</Xref>
-<Xref>PDBHET:MEN</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 8 N 2 O 2</Formula>
-<Weight type="chemical">128.13</Weight>
-<Weight type="physical">128.058578</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0003">
-<Formula>C 1 H 2 N 0 O 0</Formula>
-<Weight type="chemical">14.03</Weight>
-<Weight type="physical">14.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Klotz, A.V.</Author>
-<Author>Leary, J.A.</Author>
-<Author>Glazer, A.N.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 261, 15891-15894, 1986</Citation>
-<Title>Post-translational methylation of asparaginyl residues. Identification of beta-71 gamma-N-methylasparagine in allophycocyanin.</Title>
-<Xref>PMID:3782095</Xref>
-<Note>mass spectrometric and (1)H-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Klotz, A.V.</Author>
-<Author>Thomas, B.A.</Author>
-<Author>Glazer, A.N.</Author>
-<Author>Blacher, R.W.</Author>
-</Authors>
-<Citation>Anal. Biochem. 186, 95-100, 1990</Citation>
-<Title>Detection of methylated asparagine and glutamine residues in polypeptides.</Title>
-<Xref>DOI:10.1016/0003-2697(90)90579-X</Xref>
-<Xref>PMID:2356973</Xref>
-<Note>chemical characterization; chemical synthesis; (1)H-NMR characterization; chromatographic detection; PTH derivative</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Stec, B.</Author>
-<Author>Troxler, R.F.</Author>
-<Author>Teeter, M.M.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, June 1995</Citation>
-<Description>Structure of phycocyanin from Cyanidium caldarium at 1.65A resolution.</Description>
-<Xref>PDB:1PHN</Xref>
-<Note>X-ray diffraction, 1.65 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kettenring, J.</Author>
-<Author>Colombo, L.</Author>
-<Author>Ferrari, P.</Author>
-<Author>Tavecchia, P.</Author>
-<Author>Nebuloni, M.</Author>
-<Author>Vékey, K.</Author>
-<Author>Gallo, G.G.</Author>
-<Author>Selva, E.</Author>
-</Authors>
-<Citation>J. Antibiot. 44, 702-715, 1991</Citation>
-<Title>Antibiotic GE2270 a: a novel inhibitor of bacterial protein synthesis. II. Structure elucidation.</Title>
-<Xref>PMID:1880060</Xref>
-<Note>mass spectrometric, (1)H-NMR, (13)C-NMR, and IR identification</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>N</SequenceSpec>
-<Xref>GO:0019710</Xref>
-<Xref>PSI-MOD:00079</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>methylated amino acid</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n4-methylasparagine__n">MOD_RES N4-methylasparagine</Feature>
-</Features>
-<Image src="/images/AA0070.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0070.PDB" />
-</Entry>
-<Entry id="AA0071">
-<Header>
-<Code>AA0071</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N5-methyl-L-glutamine</Name>
-<AlternateName>2-amino-N5-methylpentanediamic acid</AlternateName>
-<AlternateName>gamma-methylglutamine</AlternateName>
-<AlternateName>N(delta)-methylglutamine</AlternateName>
-<AlternateName>N-methylglutamine</AlternateName>
-<SystematicName>(2S)-2-amino-5-methylamino-5-oxopentanoic acid</SystematicName>
-<Xref>CAS:3031-62-7</Xref>
-<Xref>ChEBI:61891</Xref>
-<Xref>PDBHET:MEQ</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 10 N 2 O 2</Formula>
-<Weight type="chemical">142.16</Weight>
-<Weight type="physical">142.074228</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0007">
-<Formula>C 1 H 2 N 0 O 0</Formula>
-<Weight type="chemical">14.03</Weight>
-<Weight type="physical">14.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lhoest, J.</Author>
-<Author>Colson, C.</Author>
-</Authors>
-<Citation>Mol. Gen. Genet. 154, 175-180, 1977</Citation>
-<Title>Genetics of ribosomal protein methylation in Escherichia coli. II. A mutant lacking a new type of methylated amino acid, N5-methylglutamine, in protein L3.</Title>
-<Xref>DOI:10.1007/BF00330833</Xref>
-<Xref>PMID:331083</Xref>
-<Note>radioisotope labeling; chromatographic identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Muranova, T.A.</Author>
-<Author>Muranov, A.V.</Author>
-<Author>Markova, L.F.</Author>
-<Author>Ovchinnikov, Y.A.</Author>
-</Authors>
-<Citation>FEBS Lett. 96, 301-305, 1978</Citation>
-<Title>The primary structure of ribosomal protein L3 from Escherichia coli 70 S ribosomes.</Title>
-<Xref>DOI:10.1016/0014-5793(78)80423-2</Xref>
-<Xref>PMID:365579</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Klotz, A.V.</Author>
-<Author>Thomas, B.A.</Author>
-<Author>Glazer, A.N.</Author>
-<Author>Blacher, R.W.</Author>
-</Authors>
-<Citation>Anal. Biochem. 186, 95-100, 1990</Citation>
-<Title>Detection of methylated asparagine and glutamine residues in polypeptides.</Title>
-<Xref>DOI:10.1016/0003-2697(90)90579-X</Xref>
-<Xref>PMID:2356973</Xref>
-<Note>chemical characterization; chemical synthesis; (1)H-NMR characterization; chromatographic detection; PTH derivative</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Dincbas-Renqvist, V.</Author>
-<Author>Engstrom, A.</Author>
-<Author>Mora, L.</Author>
-<Author>Heurgue-Hamard, V.</Author>
-<Author>Buckingham, R.</Author>
-<Author>Ehrenberg, M.</Author>
-</Authors>
-<Citation>EMBO J. 19, 6900-6907, 2000</Citation>
-<Title>A post-translational modification in the GGQ motif of RF2 from Escherichia coli stimulates termination of translation.</Title>
-<Xref>DOI:10.1093/emboj/19.24.6900</Xref>
-<Xref>PMID:11118225</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Tessarz, P.</Author>
-<Author>Santos-Rosa, H.</Author>
-<Author>Robson, S.C.</Author>
-<Author>Sylvestersen, K.B.</Author>
-<Author>Nelson, C.J.</Author>
-<Author>Nielsen, M.L.</Author>
-<Author>Kouzarides, T.</Author>
-</Authors>
-<Citation>Nature 505, 564-568, 2014</Citation>
-<Title>Glutamine methylation in histone H2A is an RNA-polymerase-I-dedicated modification.</Title>
-<Xref>DOI:10.1038/nature12819</Xref>
-<Xref>PMID:24352239</Xref>
-<Note>mass spectrometric identification</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>Q</SequenceSpec>
-<Xref>GO:0018019</Xref>
-<Xref>PSI-MOD:00080</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>methylated amino acid</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n5-methylglutamine__q">MOD_RES N5-methylglutamine</Feature>
-</Features>
-<Image src="/images/AA0071.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0071.PDB" />
-</Entry>
-<Entry id="AA0072">
-<Header>
-<Code>AA0072</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-glutamic acid 5-methyl ester</Name>
-<AlternateName>(5)-methyl L-hydrogen glutamate</AlternateName>
-<AlternateName>2-aminopentanedioic acid 5-methyl ester</AlternateName>
-<AlternateName>5-methyl L-2-aminoglutarate</AlternateName>
-<AlternateName>5-methyl L-glutamate</AlternateName>
-<AlternateName>glutamic acid 5-methyl ester</AlternateName>
-<AlternateName>glutamic acid gamma-methyl ester</AlternateName>
-<SystematicName>(2S)-2-amino-5-methoxy-5-oxopentanoic acid</SystematicName>
-<Xref>CAS:1499-55-4</Xref>
-<Xref>ChEBI:82795</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 9 N 1 O 3</Formula>
-<Weight type="chemical">143.14</Weight>
-<Weight type="physical">143.058243</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0006" label="GLU">
-<Formula>C 1 H 2 N 0 O 0</Formula>
-<Weight type="chemical">14.03</Weight>
-<Weight type="physical">14.015650</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0007" label="GLN">
-<Formula>C 1 H 1 N -1 O 1</Formula>
-<Weight type="chemical">15.01</Weight>
-<Weight type="physical">14.999666</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kleene, S.J.</Author>
-<Author>Toews, M.L.</Author>
-<Author>Adler, J.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 252, 3214-3218, 1977</Citation>
-<Title>Isolation of glutamic acid methyl ester from an Escherichia coli membrane protein involved in chemotaxis.</Title>
-<Xref>PMID:16888</Xref>
-<Note>radioisotope labeling; chromatographic detection</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kehry, M.R.</Author>
-<Author>Engstroem, P.</Author>
-<Author>Dahlquist, F.W.</Author>
-<Author>Hazelbauer, G.L.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 258, 5050-5055, 1983</Citation>
-<Title>Multiple covalent modifications of Trg, a sensory transducer of Escherichia coli.</Title>
-<Xref>PMID:6300110</Xref>
-<Note>methylated tryptic peptides were isolated</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Xiao, H.</Author>
-<Author>El Bissati, K.</Author>
-<Author>Verdier-Pinard, P.</Author>
-<Author>Burd, B.</Author>
-<Author>Zhang, H.</Author>
-<Author>Kim, K.</Author>
-<Author>Fiser, A.</Author>
-<Author>Angeletti, R.H.</Author>
-<Author>Weiss, L.M.</Author>
-</Authors>
-<Citation>J. Proteome Res. 9, 359-372, 2010</Citation>
-<Title>Post-translational modifications to Toxoplasma gondii α- and β-tubulins include novel C-terminal methylation.</Title>
-<Xref>DOI:10.1021/pr900699a</Xref>
-<Xref>PMID:19886702</Xref>
-<Note>detection of multiple glutamate methylations by mass-spectrometry in negative ion mode</Note>
-</ReferenceBlock>
-<Comment>Glutamate methylesterase can also act as a glutamine amidohydrolase.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>protein-glutamate O-methyltransferase (EC 2.1.1.80)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode link="GLU">
-<SequenceSpec>E</SequenceSpec>
-<Xref>GO:0008983</Xref>
-<Xref>GO:0018390</Xref>
-<Xref>GO:0019712</Xref>
-<Xref>PSI-MOD:00081</Xref>
-</SequenceCode>
-<SequenceCode link="GLN">
-<SequenceSpec>Q</SequenceSpec>
-<Xref>GO:0018390</Xref>
-<Xref>GO:0019713</Xref>
-<Xref>PSI-MOD:00657</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>methylated amino acid</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__glutamate methyl ester (gln)__q" link="GLN">MOD_RES Glutamate methyl ester (Gln)</Feature>
-<Feature type="UniProt" key="mod_res__glutamate methyl ester (glu)__e" link="GLU">MOD_RES Glutamate methyl ester (Glu)</Feature>
-</Features>
-<Image src="/images/AA0072.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0072.PDB" />
-</Entry>
-<Entry id="AA0073">
-<Header>
-<Code>AA0073</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-2001</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>3'-methyl-L-histidine</Name>
-<AlternateName>1-methylhistidine [misnomer]</AlternateName>
-<AlternateName>N(delta)-methylhistidine</AlternateName>
-<AlternateName>N(pi)-methylhistidine</AlternateName>
-<AlternateName>pros-methylhistidine</AlternateName>
-<SystematicName>(2S)-2-amino-3-(3-methyl-3H-imidazol-4-yl)propanoic acid</SystematicName>
-<Xref>CAS:368-16-1</Xref>
-<Xref>ChEBI:43903</Xref>
-<Xref>PDBHET:MHS</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 9 N 3 O 1</Formula>
-<Weight type="chemical">151.17</Weight>
-<Weight type="physical">151.074562</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0009">
-<Formula>C 1 H 2 N 0 O 0</Formula>
-<Weight type="chemical">14.03</Weight>
-<Weight type="physical">14.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Edmondson, D.E.</Author>
-<Author>Kenney, W.C.</Author>
-<Author>Singer, T.P.</Author>
-</Authors>
-<Citation>Biochemistry 15, 2937-2945, 1976</Citation>
-<Title>Structural elucidation and properties of 8alpha-(N1-histidyl)riboflavin: the flavin component of thiamine dehydrogenase and beta-cyclopiazonate oxidocyclase.</Title>
-<Xref>DOI:10.1021/bi00659a001</Xref>
-<Xref>PMID:8076</Xref>
-<Note>chemical and spectrographic characterization of both 1'- and 3'-methylhistidine; the authors use biochemical rather than IUPAC numbering</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Anonymous />
-<Group>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN)</Group>
-</Authors>
-<Citation>Eur. J. Biochem. 138, 9-37, 1984</Citation>
-<Title>Nomenclature and symbolism for amino acids and peptides. Recommendations 1983.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1984.tb07877.x</Xref>
-<Xref>PMID:6692818</Xref>
-<Note>tele-, tau-, and pros-, pi-, nomenclature</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Maita, T.</Author>
-<Author>Hayashida, M.</Author>
-<Author>Tanioka, Y.</Author>
-<Author>Komine, Y.</Author>
-<Author>Matsuda, G.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 84, 416-420, 1987</Citation>
-<Title>The primary structure of the myosin head.</Title>
-<Xref>DOI:10.1073/pnas.84.2.416</Xref>
-<Xref>PMID:3467365</Xref>
-<Note>identification of 3'-methylhistidine along with methyl- and trimethyllysine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Raftery, M.J.</Author>
-<Author>Harrison, C.A.</Author>
-<Author>Alewood, P.</Author>
-<Author>Jones, A.</Author>
-<Author>Geczy, C.L.</Author>
-</Authors>
-<Citation>Biochem. J. 316, 285-293, 1996</Citation>
-<Title>Isolation of the murine S100 protein MRP14 (14 kDa migration-inhibitory-factor-related protein) from activated spleen cells: characterization of post-translational modifications and zinc binding.</Title>
-<Xref>PMID:8645219</Xref>
-<Note>mass spectrometric detection; chromatographic identification of PTC derivatives of 1'- and 3'-methylhistidine; the authors' source for the reference standard acknowledges that their name, 1'-methylhistidine, is a misnomer for the IUPAC standard name 3'-methylhistidine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Selmer, T.</Author>
-<Author>Kahnt, J.</Author>
-<Author>Goubeaud, M.</Author>
-<Author>Shima, S.</Author>
-<Author>Grabarse, W.</Author>
-<Author>Ermler, U.</Author>
-<Author>Thauer, R.K.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 275, 3755-3760, 2000</Citation>
-<Title>The biosynthesis of methylated amino acids in the active site region of methyl-coenzyme M reductase.</Title>
-<Xref>DOI:10.1074/jbc.275.6.3755</Xref>
-<Xref>PMID:10660523</Xref>
-<Note>mass spectrometric characterization; in methyl-coenzyme M reductase the biosynthetic origin of the methyl group is S-adenosyl methionine, not methyl-coenzyme M</Note>
-</ReferenceBlock>
-<Comment>In the older biochemical literature this is usually called 1-methylhistidine. See also RESID:AA0317.</Comment>
-<Comment>The crystallographic designation for the substituted nitrogen is delta-1, D1.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>protein-L-histidine N-pros-methyltransferase (EC 2.1.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>H</SequenceSpec>
-<Xref>GO:0018021</Xref>
-<Xref>GO:0042037</Xref>
-<Xref>PSI-MOD:00082</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>methylated amino acid</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__pros-methylhistidine__h">MOD_RES Pros-methylhistidine</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="mod_res__methylhistidine__h">MOD_RES Methylhistidine</Feature>
-<Note>this UniProt feature is used when the isomeric structure has not been determined</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0073.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0073.PDB" />
-</Entry>
-<Entry id="AA0074">
-<Header>
-<Code>AA0074</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-Dec-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6,N6,N6-trimethyl-L-lysine</Name>
-<AlternateName>2-amino-6-(trimethylammonio)hexanoic acid</AlternateName>
-<AlternateName>5-azanyl-5-carboxy-N,N,N-trimethylpentanazanium</AlternateName>
-<AlternateName>epsilon-trimethyllysine</AlternateName>
-<AlternateName>N(zeta)-trimethyllysine</AlternateName>
-<AlternateName>N6,N6,N6-trimethyllysin-N6-ium</AlternateName>
-<AlternateName>N6,N6,N6-trimethyllysine cation</AlternateName>
-<SystematicName>(5S)-5-amino-5-carboxy-N,N,N-trimethylpentan-1-aminium</SystematicName>
-<Xref>CAS:19253-88-4</Xref>
-<Xref>ChEBI:61961</Xref>
-<Xref>PDBHET:M3L</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 19 N 2 O 1</Formula>
-<FormalCharge>1+</FormalCharge>
-<Weight type="chemical">171.26</Weight>
-<Weight type="physical">171.149190</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 3 H 7 N 0 O 0</Formula>
-<FormalCharge>1+</FormalCharge>
-<Weight type="chemical">43.09</Weight>
-<Weight type="physical">43.054227</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>DeLange, R.J.</Author>
-<Author>Glazer, A.N.</Author>
-<Author>Smith, E.L.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 244, 1385-1388, 1969</Citation>
-<Title>Presence and location of an unusual amino acid, epsilon-N-trimethyllysine, in cytochrome c of wheat germ and Neurospora.</Title>
-<Xref>PMID:4304194</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Dognin, M.J.</Author>
-<Author>Wittmann-Liebold, B.</Author>
-</Authors>
-<Citation>Hoppe-Seyler's Z. Physiol. Chem. 361, 1697-1705, 1980</Citation>
-<Title>Identification of methylated amino acids during sequence analysis. Application to the Escherichia coli ribosomal protein L11.</Title>
-<Xref>DOI:10.1515/bchm2.1980.361.2.1697</Xref>
-<Xref>PMID:6778808</Xref>
-<Note>chromatographic detection; mass spectrometric identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bloxham, D.P.</Author>
-<Author>Parmelee, D.C.</Author>
-<Author>Kumar, S.</Author>
-<Author>Walsh, K.A.</Author>
-<Author>Titani, K.</Author>
-</Authors>
-<Citation>Biochemistry 21, 2028-2036, 1982</Citation>
-<Title>Complete amino acid sequence of porcine heart citrate synthase.</Title>
-<Xref>DOI:10.1021/bi00538a009</Xref>
-<Xref>PMID:7093227</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Babu, Y.S.</Author>
-<Author>Bugg, C.E.</Author>
-<Author>Cook, W.J.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, May 1988</Citation>
-<Description>Structure of calmodulin refined at 2.2 A resolution.</Description>
-<Xref>PDB:3CLN</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Babu, Y.S.</Author>
-<Author>Bugg, C.E.</Author>
-<Author>Cook, W.J.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 204, 191-204, 1988</Citation>
-<Title>Structure of calmodulin refined at 2.2 A resolution.</Title>
-<Xref>DOI:10.1016/0022-2836(88)90608-0</Xref>
-<Xref>PMID:3145979</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sundaralingam, M.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, August 1993</Citation>
-<Description>Structure of the recombinant Paramecium tetraurelia calmodulin at 1.68 Angstrom resolution.</Description>
-<Xref>PDB:1OSA</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Rao, S.T.</Author>
-<Author>Wu, S.</Author>
-<Author>Satyshur, K.A.</Author>
-<Author>Ling, K.Y.</Author>
-<Author>Kung, C.</Author>
-<Author>Sundaralingam, M.</Author>
-</Authors>
-<Citation>Protein Sci. 2, 436-447, 1993</Citation>
-<Title>Structure of Paramecium tetraurelia calmodulin at 1.8 angstroms resolution.</Title>
-<Xref>DOI:10.1002/pro.5560020316</Xref>
-<Xref>PMID:8453381</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hirota, J.</Author>
-<Author>Satomi, Y.</Author>
-<Author>Yoshikawa, K.</Author>
-<Author>Takao, T.</Author>
-</Authors>
-<Citation>Rapid Commun. Mass Spectrom. 17, 371-376, 2003</Citation>
-<Title>Epsilon-N,N,N-trimethyllysine-specific ions in matrix-assisted laser desorption/ionization-tandem mass spectrometry.</Title>
-<Xref>DOI:10.1002/rcm.924</Xref>
-<Xref>PMID:12590383</Xref>
-<Note>attempts to distinguish from nominally isobaric N6-acetyllysine (see RESID:AA0055); the authors say trimethylation "causes an incremental increase in mass of 42.0470 Da from the corresponding MH+ ion"; the correct value to four decimal places is 43.0542 when the difference is taken instead from the neutral parent mass as all other difference calculations are</Note>
-</ReferenceBlock>
-<Comment>Consult FAQ at http://pir.georgetown.edu/resid/faq.shtml#q12 concerning calculation of the difference formula.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>histone-lysine N-methyltransferase (EC 2.1.1.43)</EnzymeName>
-<EnzymeName>cytochrome-c-lysine N-methyltransferase (EC 2.1.1.59)</EnzymeName>
-<EnzymeName>calmodulin-lysine N-methyltransferase (EC 2.1.1.60)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>GO:0018023</Xref>
-<Xref>GO:0018024</Xref>
-<Xref>PSI-MOD:00083</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>methylated amino acid</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n6,n6,n6-trimethyllysine__k">MOD_RES N6,N6,N6-trimethyllysine</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="mod_res__n6-methylated lysine__k">MOD_RES N6-methylated lysine</Feature>
-<Note>this UniProt feature is used when the extent of methylation has not been determined</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0074.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0074.PDB" />
-</Entry>
-<Entry id="AA0075">
-<Header>
-<Code>AA0075</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-Dec-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6,N6-dimethyl-L-lysine</Name>
-<AlternateName>epsilon-dimethyllysine</AlternateName>
-<AlternateName>lysine derivative Lys(y)</AlternateName>
-<AlternateName>N(zeta)-dimethyllysine</AlternateName>
-<SystematicName>(2S)-2-amino-6-(dimethylamino)hexanoic acid</SystematicName>
-<Xref>CAS:2259-86-1</Xref>
-<Xref>ChEBI:61969</Xref>
-<Xref>PDBHET:MLY</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 8 H 16 N 2 O 1</Formula>
-<Weight type="chemical">156.23</Weight>
-<Weight type="physical">156.126263</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 2 H 4 N 0 O 0</Formula>
-<Weight type="chemical">28.05</Weight>
-<Weight type="physical">28.031300</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Schaefer, W.H.</Author>
-<Author>Lukas, T.J.</Author>
-<Author>Blair, I.A.</Author>
-<Author>Schultz, J.E.</Author>
-<Author>Watterson, D.M.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 262, 1025-1029, 1987</Citation>
-<Title>Amino acid sequence of a novel calmodulin from Paramecium tetraurelia that contains dimethyllysine in the first domain.</Title>
-<Xref>PMID:3100523</Xref>
-<Note>mass spectrometric identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sundaralingam, M.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, August 1993</Citation>
-<Description>Structure of the recombinant Paramecium tetraurelia calmodulin at 1.68 Angstrom resolution.</Description>
-<Xref>PDB:1OSA</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Rao, S.T.</Author>
-<Author>Wu, S.</Author>
-<Author>Satyshur, K.A.</Author>
-<Author>Ling, K.Y.</Author>
-<Author>Kung, C.</Author>
-<Author>Sundaralingam, M.</Author>
-</Authors>
-<Citation>Protein Sci. 2, 436-447, 1993</Citation>
-<Title>Structure of Paramecium tetraurelia calmodulin at 1.8 angstroms resolution.</Title>
-<Xref>DOI:10.1002/pro.5560020316</Xref>
-<Xref>PMID:8453381</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Rayment, I.</Author>
-<Author>Rypniewski, W.R.</Author>
-<Author>Schmidt-Bäse, K.</Author>
-<Author>Smith, R.</Author>
-<Author>Tomchick, D.R.</Author>
-<Author>Benning, M.M.</Author>
-<Author>Winkelmann, D.A.</Author>
-<Author>Wesenberg, G.</Author>
-<Author>Holden, H.M.</Author>
-</Authors>
-<Citation>Science 261, 50-58, 1993</Citation>
-<Title>Three-dimensional structure of myosin subfragment-1: a molecular motor.</Title>
-<Xref>DOI:10.1126/science.8316857</Xref>
-<Xref>PMID:8316857</Xref>
-<Note>chemical method for specific dimthylation of lysine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kroeger, N.</Author>
-<Author>Deutzmann, R.</Author>
-<Author>Sumper, M.</Author>
-</Authors>
-<Citation>Science 286, 1129-1132, 1999</Citation>
-<Title>Polycationic peptides from diatom biosilica that direct silica nanosphere formation.</Title>
-<Xref>DOI:10.1126/science.286.5442.1129</Xref>
-<Xref>PMID:10550045</Xref>
-<Note>chromatographic, mass spectrometric and (1)H-NMR identification</Note>
-</ReferenceBlock>
-<Comment>This modification is readily formed artifactually by reductive methylation using formaldehyde.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>histone-lysine N-methyltransferase (EC 2.1.1.43)</EnzymeName>
-<EnzymeName>cytochrome-c-lysine N-methyltransferase (EC 2.1.1.59)</EnzymeName>
-<EnzymeName>calmodulin-lysine N-methyltransferase (EC 2.1.1.60)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>GO:0018024</Xref>
-<Xref>GO:0018027</Xref>
-<Xref>PSI-MOD:00084</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>methylated amino acid</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n6,n6-dimethyllysine__k">MOD_RES N6,N6-dimethyllysine</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="mod_res__n6-methylated lysine__k">MOD_RES N6-methylated lysine</Feature>
-<Note>this UniProt feature is used when the extent of methylation has not been determined</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0075.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0075.PDB" />
-</Entry>
-<Entry id="AA0076">
-<Header>
-<Code>AA0076</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6-methyl-L-lysine</Name>
-<AlternateName>epsilon-methyllysine</AlternateName>
-<AlternateName>N(zeta)-methyllysine</AlternateName>
-<SystematicName>(2S)-2-amino-6-methylaminohexanoic acid</SystematicName>
-<Xref>CAS:1188-07-4</Xref>
-<Xref>ChEBI:61928</Xref>
-<Xref>PDBHET:MLZ</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 14 N 2 O 1</Formula>
-<Weight type="chemical">142.20</Weight>
-<Weight type="physical">142.110613</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 1 H 2 N 0 O 0</Formula>
-<Weight type="chemical">14.03</Weight>
-<Weight type="physical">14.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Minami, Y.</Author>
-<Author>Wakabayashi, S.</Author>
-<Author>Wada, K.</Author>
-<Author>Matsubara, H.</Author>
-<Author>Kerscher, L.</Author>
-<Author>Oesterhelt, D.</Author>
-</Authors>
-<Citation>J. Biochem. 97, 745-753, 1985</Citation>
-<Title>Amino acid sequence of a ferredoxin from thermoacidophilic archaebacterium, Sulfolobus acidocaldarius. Presence of an N(6)-monomethyllysine and phyletic consideration of archaebacteria.</Title>
-<Xref>PMID:3926756</Xref>
-<Note>chromatographic and mass spectrometric identification</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>histone-lysine N-methyltransferase (EC 2.1.1.43)</EnzymeName>
-<EnzymeName>cytochrome-c-lysine N-methyltransferase (EC 2.1.1.59)</EnzymeName>
-<EnzymeName>calmodulin-lysine N-methyltransferase (EC 2.1.1.60)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>GO:0018024</Xref>
-<Xref>GO:0018026</Xref>
-<Xref>PSI-MOD:00085</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>methylated amino acid</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n6-methyllysine__k">MOD_RES N6-methyllysine</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="mod_res__n6-methylated lysine__k">MOD_RES N6-methylated lysine</Feature>
-<Note>this UniProt feature is used when the extent of methylation has not been determined</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0076.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0076.PDB" />
-</Entry>
-<Entry id="AA0077">
-<Header>
-<Code>AA0077</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6-palmitoyl-L-lysine</Name>
-<AlternateName>2-amino-6-(hexadecanamido)hexanoic acid</AlternateName>
-<AlternateName>epsilon-palmitoyllysine</AlternateName>
-<AlternateName>N(zeta)-palmitoyllysine</AlternateName>
-<AlternateName>N6-(1-oxohexadecyl)-L-lysine</AlternateName>
-<SystematicName>(2S)-2-amino-6-(hexadecanoylamino)hexanoic acid</SystematicName>
-<Xref>CAS:559012-43-0</Xref>
-<Xref>ChEBI:21895</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 22 H 42 N 2 O 2</Formula>
-<Weight type="chemical">366.59</Weight>
-<Weight type="physical">366.324629</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 16 H 30 N 0 O 1</Formula>
-<Weight type="chemical">238.41</Weight>
-<Weight type="physical">238.229666</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Tomasselli, A.G.</Author>
-<Author>Hui, J.</Author>
-<Author>Fisher, J.</Author>
-<Author>Zuercher-Neely, H.</Author>
-<Author>Reardon, I.M.</Author>
-<Author>Oriaku, E.</Author>
-<Author>Kezdy, F.J.</Author>
-<Author>Heinrikson, R.L.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 264, 10041-10047, 1989</Citation>
-<Title>Dimerization and activation of porcine pancreatic phospholipase A2 via substrate level acylation of lysine 56.</Title>
-<Xref>PMID:2498336</Xref>
-<Note>the autocatalytic transfer of a fatty acid, normally palmitate, from substrate to lysine is described; octanoate transfer from a chromogenic substrate analog is artifactual</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hackett, M.</Author>
-<Author>Guo, L.</Author>
-<Author>Shabanowitz, J.</Author>
-<Author>Hunt, D.F.</Author>
-<Author>Hewlett, E.L.</Author>
-</Authors>
-<Citation>Science 266, 433-435, 1994</Citation>
-<Title>Internal lysine palmitoylation in adenylate cyclase toxin from Bordetella pertussis.</Title>
-<Xref>DOI:10.1126/science.7939682</Xref>
-<Xref>PMID:7939682</Xref>
-<Note>mass spectrometric identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Stanley, P.</Author>
-<Author>Packman, L.C.</Author>
-<Author>Koronakis, V.</Author>
-<Author>Hughes, C.</Author>
-</Authors>
-<Citation>Science 266, 1992-1996, 1994</Citation>
-<Title>Fatty acylation of two internal lysine residues required for the toxic activity of Escherichia coli hemolysin.</Title>
-<Xref>DOI:10.1126/science.7801126</Xref>
-<Xref>PMID:7801126</Xref>
-<Note>radioisotope labeling</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Jiang, H.</Author>
-<Author>Khan, S.</Author>
-<Author>Wang, Y.</Author>
-<Author>Charron, G.</Author>
-<Author>He, B.</Author>
-<Author>Sebastian, C.</Author>
-<Author>Du, J.</Author>
-<Author>Kim, R.</Author>
-<Author>Ge, E.</Author>
-<Author>Mostoslavsky, R.</Author>
-<Author>Hang, H.C.</Author>
-<Author>Hao, Q.</Author>
-<Author>Lin, H.</Author>
-</Authors>
-<Citation>Nature 496, 110-113, 2013</Citation>
-<Title>SIRT6 regulates TNF-α secretion through hydrolysis of long-chain fatty acyl lysine.</Title>
-<Xref>DOI:10.1038/nature12038</Xref>
-<Xref>PMID:23552949</Xref>
-<Note>hydrolase from an infective organism that preferentially removes myristoyl and palmitoyl groups from N6-acylated lysine peptides</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>peptidyl-lysine N6-palmitoyltransferase (EC 2.3.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>GO:0018029</Xref>
-<Xref>PSI-MOD:00086</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lipoprotein</Keyword>
-<Keyword>palmitoylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__n6-palmitoyl lysine__k">LIPID N6-palmitoyl lysine</Feature>
-</Features>
-<Image src="/images/AA0077.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0077.PDB" />
-</Entry>
-<Entry id="AA0078">
-<Header>
-<Code>AA0078</Code>
-<Dates>
-<CreationDate>09-Aug-1995</CreationDate>
-<StrucRevDate>09-Aug-1995</StrucRevDate>
-<TextChngDate>31-May-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6-myristoyl-L-lysine</Name>
-<AlternateName>2-amino-6-(tetradecanamido)hexanoic acid</AlternateName>
-<AlternateName>epsilon-myristoyllysine</AlternateName>
-<AlternateName>N(zeta)-myristoyllysine</AlternateName>
-<AlternateName>N6-(1-oxotetradecyl)-L-lysine</AlternateName>
-<SystematicName>(2S)-2-amino-6-(tetradecanoylamino)hexanoic acid</SystematicName>
-<Xref>CAS:62471-07-2</Xref>
-<Xref>ChEBI:21894</Xref>
-<Xref>PDBHET:MYK</Xref>
-<Xref>PDBHET:MYR</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 20 H 38 N 2 O 2</Formula>
-<Weight type="chemical">338.54</Weight>
-<Weight type="physical">338.293328</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 14 H 26 N 0 O 1</Formula>
-<Weight type="chemical">210.36</Weight>
-<Weight type="physical">210.198365</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Stevenson, F.T.</Author>
-<Author>Bursten, S.L.</Author>
-<Author>Locksley, R.M.</Author>
-<Author>Lovett, D.H.</Author>
-</Authors>
-<Citation>J. Exp. Med. 176, 1053-1062, 1992</Citation>
-<Title>Myristyl acylation of the tumor necrosis factor alpha precursor on specific lysine residues.</Title>
-<Xref>DOI:10.1084/jem.176.4.1053</Xref>
-<Xref>PMID:1402651</Xref>
-<Note>radioisotope labeling; biosynthesis; chromatographic detection</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Stevenson, F.T.</Author>
-<Author>Bursten, S.L.</Author>
-<Author>Fanton, C.</Author>
-<Author>Locksley, R.M.</Author>
-<Author>Lovett, D.H.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 90, 7245-7249, 1993</Citation>
-<Title>The 31-kDa precursor of interleukin 1alpha is myristoylated on specific lysines within the 16-kDa N-terminal propiece.</Title>
-<Xref>DOI:10.1073/pnas.90.15.7245</Xref>
-<Xref>PMID:8346241</Xref>
-<Note>biosynthesis; chemical synthesis; chromatographic detection</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Whittingham, J.L.</Author>
-<Author>Havelund, S.</Author>
-<Author>Jonassen, I.</Author>
-</Authors>
-<Citation>Biochemistry 36, 2826-2831, 1997</Citation>
-<Title>Crystal structure of a prolonged-acting insulin with albumin-binding properties.</Title>
-<Xref>DOI:10.1021/bi9625105</Xref>
-<Xref>PMID:9062110</Xref>
-<Note>crystallographic structure of artifically produced modification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Whittingham, J.L.</Author>
-<Author>Havelund, S.</Author>
-<Author>Jonassen, I.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, December 1996</Citation>
-<Description>Structure of insulin.</Description>
-<Xref>PDB:1XDA</Xref>
-<Note>X-ray diffraction, 1.80 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Jiang, H.</Author>
-<Author>Khan, S.</Author>
-<Author>Wang, Y.</Author>
-<Author>Charron, G.</Author>
-<Author>He, B.</Author>
-<Author>Sebastian, C.</Author>
-<Author>Du, J.</Author>
-<Author>Kim, R.</Author>
-<Author>Ge, E.</Author>
-<Author>Mostoslavsky, R.</Author>
-<Author>Hang, H.C.</Author>
-<Author>Hao, Q.</Author>
-<Author>Lin, H.</Author>
-</Authors>
-<Citation>Nature 496, 110-113, 2013</Citation>
-<Title>SIRT6 regulates TNF-α secretion through hydrolysis of long-chain fatty acyl lysine.</Title>
-<Xref>DOI:10.1038/nature12038</Xref>
-<Xref>PMID:23552949</Xref>
-<Note>hydrolase from an infective organism that preferentially removes myristoyl and palmitoyl groups from N6-acylated lysine peptides</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>peptidyl-lysine N6-myristoyltransferase (EC 2.3.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>GO:0018028</Xref>
-<Xref>PSI-MOD:00087</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lipoprotein</Keyword>
-<Keyword>myristoylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__n6-myristoyl lysine__k">LIPID N6-myristoyl lysine</Feature>
-</Features>
-<Image src="/images/AA0078.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0078.PDB" />
-</Entry>
-<Entry id="AA0079">
-<Header>
-<Code>AA0079</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-palmitoyl-L-threonine</Name>
-<AlternateName>L-threonine hexadecanoate ester</AlternateName>
-<AlternateName>O3-palmitoyl-threonine</AlternateName>
-<AlternateName>threonine palmitate ester</AlternateName>
-<SystematicName>(2S,3R)-2-amino-3-(hexadecanoyloxy)butanoic acid</SystematicName>
-<Xref>CAS:88467-30-5</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 20 H 37 N 1 O 3</Formula>
-<Weight type="chemical">339.52</Weight>
-<Weight type="physical">339.277344</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0017">
-<Formula>C 16 H 30 N 0 O 1</Formula>
-<Weight type="chemical">238.41</Weight>
-<Weight type="physical">238.229666</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Stoffel, W.</Author>
-<Author>Hillen, H.</Author>
-<Author>Schroeder, W.</Author>
-<Author>Deutzmann, R.</Author>
-</Authors>
-<Citation>Hoppe-Seyler's Z. Physiol. Chem. 364, 1455-1466, 1983</Citation>
-<Title>The primary structure of bovine brain myelin lipophilin (proteolipid apoprotein).</Title>
-<Xref>DOI:10.1515/bchm2.1983.364.2.1455</Xref>
-<Xref>PMID:6642431</Xref>
-<Note>chromatographic and mass spectrometric identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Branton, W.D.</Author>
-<Author>Rudnick, M.S.</Author>
-<Author>Zhou, Y.</Author>
-<Author>Eccleston, E.D.</Author>
-<Author>Fields, G.B.</Author>
-<Author>Bowers, L.D.</Author>
-</Authors>
-<Citation>Nature 365, 496-497, 1993</Citation>
-<Title>Fatty acylated toxin structure.</Title>
-<Xref>DOI:10.1038/365496a0</Xref>
-<Xref>PMID:8413602</Xref>
-<Note>chromatographic and mass spectrometric identification</Note>
-</ReferenceBlock>
-<Comment>The palmitate represents a mixture of saturated and unsaturated fatty acids.</Comment>
-<SequenceCode>
-<SequenceSpec>T</SequenceSpec>
-<Condition>incidental to RESID:AA0097</Condition>
-<Xref>GO:0018220</Xref>
-<Xref>PSI-MOD:00088</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lipoprotein</Keyword>
-<Keyword>palmitoylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__o-palmitoyl threonine__t">LIPID O-palmitoyl threonine</Feature>
-</Features>
-<Image src="/images/AA0079.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0079.PDB" />
-</Entry>
-<Entry id="AA0080">
-<Header>
-<Code>AA0080</Code>
-<Dates>
-<CreationDate>25-Aug-1995</CreationDate>
-<StrucRevDate>25-Aug-1995</StrucRevDate>
-<TextChngDate>30-Sep-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-palmitoyl-L-serine</Name>
-<AlternateName>L-serine hexadecanoate ester</AlternateName>
-<AlternateName>O3-palmitoyl-serine</AlternateName>
-<AlternateName>serine palmitate ester</AlternateName>
-<SystematicName>(2S)-2-amino-3-(hexadecanoyloxy)propanoic acid</SystematicName>
-<Xref>CAS:88815-78-5</Xref>
-<Xref>PDBHET:PLM</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 19 H 35 N 1 O 3</Formula>
-<Weight type="chemical">325.49</Weight>
-<Weight type="physical">325.261694</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 16 H 30 N 0 O 1</Formula>
-<Weight type="chemical">238.41</Weight>
-<Weight type="physical">238.229666</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Diehl, H.J.</Author>
-<Author>Schaich, M.</Author>
-<Author>Budzinski, R.M.</Author>
-<Author>Stoffel, W.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 83, 9807-9811, 1986</Citation>
-<Title>Individual exons encode the integral membrane domains of human myelin proteolipid protein.</Title>
-<Xref>DOI:10.1073/pnas.83.24.9807</Xref>
-<Xref>PMID:3467339</Xref>
-<Note>the fatty acid attachment site is shown without evidence</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bellizzi 3rd, J.J.</Author>
-<Author>Widom, J.</Author>
-<Author>Kemp, C.</Author>
-<Author>Lu, J.Y.</Author>
-<Author>Das, A.K.</Author>
-<Author>Hofmann, S.L.</Author>
-<Author>Clardy, J.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 97, 4573-4578, 2000</Citation>
-<Title>The crystal structure of palmitoyl protein thioesterase 1 and the molecular basis of infantile neuronal ceroid lipofuscinosis.</Title>
-<Xref>DOI:10.1073/pnas.080508097</Xref>
-<Xref>PMID:10781062</Xref>
-<Note>X-ray diffraction, 2.50 angstroms; active site intermediate</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bellizzi 3rd, J.J.</Author>
-<Author>Widom, J.</Author>
-<Author>Kemp, C.</Author>
-<Author>Lu, J.Y.</Author>
-<Author>Das, A.K.</Author>
-<Author>Hofmann, S.L.</Author>
-<Author>Clardy, J.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, February 2000</Citation>
-<Description>Crystal structure of palmitoyl protein thioesterase 1 complexed with palmitate.</Description>
-<Xref>PDB:1EH5</Xref>
-<Note>X-ray diffraction, 2.50 angstroms; active site intermediate</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Zou, C.</Author>
-<Author>Ellis, B.M.</Author>
-<Author>Smith, R.M.</Author>
-<Author>Chen, B.B.</Author>
-<Author>Zhao, Y.</Author>
-<Author>Mallampalli, R.K.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 286, 28019-28025, 2011</Citation>
-<Title>Acyl-CoA:lysophosphatidylcholine acyltransferase I (Lpcat1) catalyzes histone protein O-palmitoylation to regulate mRNA synthesis.</Title>
-<Xref>DOI:10.1074/jbc.M111.253385</Xref>
-<Xref>PMID:21685381</Xref>
-<Note>radiolabeling with palmitoyl CoA; Lpcat1 migrated to nuclei during exogenous calcium flux and specifically modified histone H4</Note>
-</ReferenceBlock>
-<Comment>The palmitate represents a mixture of saturated and unsaturated fatty acids.</Comment>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>GO:0018221</Xref>
-<Xref>PSI-MOD:00089</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lipoprotein</Keyword>
-<Keyword>palmitoylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__o-palmitoyl serine__s">LIPID O-palmitoyl serine</Feature>
-<Feature type="UniProt" key="act_site__o-palmitoyl serine intermediate__s">ACT_SITE O-palmitoyl serine intermediate</Feature>
-</Features>
-<Image src="/images/AA0080.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0080.PDB" />
-</Entry>
-<Entry id="AA0081">
-<Header>
-<Code>AA0081</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-alanine amide</Name>
-<AlternateName>alaninamide</AlternateName>
-<SystematicName>(2S)-2-aminopropanamide</SystematicName>
-<Xref>CAS:7324-05-2</Xref>
-<Xref>ChEBI:21217</Xref>
-<Xref>PDBHET:NH2</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 7 N 2 O 1</Formula>
-<Weight type="chemical">87.10</Weight>
-<Weight type="physical">87.055838</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0001">
-<Formula>C 0 H 1 N 1 O -1</Formula>
-<Weight type="chemical">-0.98</Weight>
-<Weight type="physical">-0.984016</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fernlund, P.</Author>
-</Authors>
-<Citation>Biochim. Biophys. Acta 439, 17-25, 1976</Citation>
-<Title>Structure of a light-adapting hormone from the shrimp, Pandalus borealis.</Title>
-<Xref>DOI:10.1016/0005-2795(76)90155-0</Xref>
-<Xref>PMID:952951</Xref>
-<Note>chromatographic identification of dansyl derivative</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lancelin, J.M.</Author>
-<Author>Kohda, D.</Author>
-<Author>Tate, S.I.</Author>
-<Author>Yanagawa, Y.</Author>
-<Author>Abe, T.</Author>
-<Author>Satake, M.</Author>
-<Author>Inagaki, F.</Author>
-</Authors>
-<Citation>Biochemistry 30, 6908-6916, 1991</Citation>
-<Title>Tertiary structure of conotoxin GIIIA in aqueous solution.</Title>
-<Xref>DOI:10.1021/bi00242a014</Xref>
-<Xref>PMID:2069951</Xref>
-<Note>(1)H-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lohr, J.</Author>
-<Author>Klein, J.</Author>
-<Author>Webster, S.G.</Author>
-<Author>Dircksen, H.</Author>
-</Authors>
-<Citation>Comp. Biochem. Physiol., B 104, 699-706, 1993</Citation>
-<Title>Quantification, immunoaffinity purification and sequence analysis of a pigment-dispersing hormone of the shore crab, Carcinus maenas (L.).</Title>
-<Xref>DOI:10.1016/0305-0491(93)90200-O</Xref>
-<Xref>PMID:8472537</Xref>
-<Note>mass spectrometric characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Takamatsu, K.</Author>
-<Author>Tatemoto, K.</Author>
-</Authors>
-<Citation>Neurochem. Res. 17, 239-246, 1992</Citation>
-<Title>Isolation and characterization of two novel peptide amides originating from myelin basic protein in bovine brain.</Title>
-<Xref>DOI:10.1007/BF00966665</Xref>
-<Xref>PMID:1377792</Xref>
-<Note>this peptide has a carboxyl-terminal amide probably produced by a non-enzymatic reaction</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>peptidylglycine monooxygenase (EC 1.14.17.3)</EnzymeName>
-<EnzymeName>peptidylamidoglycolate lyase (EC 4.3.2.5)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>A</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0018034</Xref>
-<Xref>PSI-MOD:00090</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>amidated carboxyl end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__alanine amide__a">MOD_RES Alanine amide</Feature>
-</Features>
-<Image src="/images/AA0081.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0081.PDB" />
-</Entry>
-<Entry id="AA0082">
-<Header>
-<Code>AA0082</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-arginine amide</Name>
-<AlternateName>2-amino-5-carbamimidamidopentanamide</AlternateName>
-<AlternateName>2-amino-5-guanidinopentanamide</AlternateName>
-<AlternateName>argininamide</AlternateName>
-<SystematicName>(2S)-2-amino-5-[(diaminomethylidene)amino]pentanamide</SystematicName>
-<Xref>CAS:2788-83-2</Xref>
-<Xref>ChEBI:21236</Xref>
-<Xref>PDBHET:AAR</Xref>
-<Xref>PDBHET:NH2</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 14 N 5 O 1</Formula>
-<Weight type="chemical">172.21</Weight>
-<Weight type="physical">172.119835</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0002">
-<Formula>C 0 H 1 N 1 O -1</Formula>
-<Weight type="chemical">-0.98</Weight>
-<Weight type="physical">-0.984016</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Maeda, N.</Author>
-<Author>Tamiya, N.</Author>
-</Authors>
-<Citation>Biochem. J. 175, 507-517, 1978</Citation>
-<Title>Three neurotoxins from the venom of a sea snake Astrotia stokesii, including two long-chain neurotoxic proteins with amidated C-termini.</Title>
-<Xref>PMID:743209</Xref>
-<Note>chromatographic identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Orskov, C.</Author>
-<Author>Bersani, M.</Author>
-<Author>Johnsen, A.H.</Author>
-<Author>Højrup, P.</Author>
-<Author>Holst, J.J.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 264, 12826-12829, 1989</Citation>
-<Title>Complete sequences of glucagon-like peptide-1 from human and pig small intestine.</Title>
-<Xref>PMID:2753890</Xref>
-<Note>mass spectrometric identification by differential methyl esterification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Muta, T.</Author>
-<Author>Fujimoto, T.</Author>
-<Author>Nakajima, H.</Author>
-<Author>Iwanaga, S.</Author>
-</Authors>
-<Citation>J. Biochem. 108, 261-266, 1990</Citation>
-<Title>Tachyplesins isolated from hemocytes of southeast Asian horseshoe crabs (Carcinoscorpius rotundicauda and Tachypleus gigas): identification of a new tachyplesin, tachyplesin III, and a processing intermediate of its precursor.</Title>
-<Xref>PMID:2229025</Xref>
-<Note>chromatographic identification of the phenylthiocarbamyl derivative</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>peptidylglycine monooxygenase (EC 1.14.17.3)</EnzymeName>
-<EnzymeName>peptidylamidoglycolate lyase (EC 4.3.2.5)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>R</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0018035</Xref>
-<Xref>PSI-MOD:00091</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>amidated carboxyl end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__arginine amide__r">MOD_RES Arginine amide</Feature>
-</Features>
-<Image src="/images/AA0082.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0082.PDB" />
-</Entry>
-<Entry id="AA0083">
-<Header>
-<Code>AA0083</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-asparagine amide</Name>
-<AlternateName>asparaginamide</AlternateName>
-<SystematicName>(2S)-2-aminobutanediamide</SystematicName>
-<Xref>CAS:16748-73-5</Xref>
-<Xref>ChEBI:21243</Xref>
-<Xref>PDBHET:NH2</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 8 N 3 O 2</Formula>
-<Weight type="chemical">130.13</Weight>
-<Weight type="physical">130.061652</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0003">
-<Formula>C 0 H 1 N 1 O -1</Formula>
-<Weight type="chemical">-0.98</Weight>
-<Weight type="physical">-0.984016</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Tatemoto, K.</Author>
-<Author>Mutt, V.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 75, 4115-4119, 1978</Citation>
-<Title>Chemical determination of polypeptide hormones.</Title>
-<Xref>DOI:10.1073/pnas.75.9.4115</Xref>
-<Xref>PMID:279902</Xref>
-<Note>chromatographic identification of the dansyl derivatives of most of the amino acid amides</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Jaffe, H.</Author>
-<Author>Raina, A.K.</Author>
-<Author>Riley, C.T.</Author>
-<Author>Fraser, B.A.</Author>
-<Author>Bird, T.G.</Author>
-<Author>Tseng, C.M.</Author>
-<Author>Zhang, Y.S.</Author>
-<Author>Hayes, D.K.</Author>
-</Authors>
-<Citation>Biochem. Biophys. Res. Commun. 155, 344-350, 1988</Citation>
-<Title>Isolation and primary structure of a neuropeptide hormone from Heliothis zea with hypertrehalosemic and adipokinetic activities.</Title>
-<Xref>DOI:10.1016/S0006-291X(88)81091-X</Xref>
-<Xref>PMID:3415690</Xref>
-<Note>mass spectrometric detection</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Veenstra, J.A.</Author>
-</Authors>
-<Citation>FEBS Lett. 250, 231-234, 1989</Citation>
-<Title>Isolation and structure of corazonin, a cardioactive peptide from the american cockroach.</Title>
-<Xref>DOI:10.1016/0014-5793(89)80727-6</Xref>
-<Xref>PMID:2753132</Xref>
-<Note>chromatographic identification of the phenylthiocarbamyl derivative</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>peptidylglycine monooxygenase (EC 1.14.17.3)</EnzymeName>
-<EnzymeName>peptidylamidoglycolate lyase (EC 4.3.2.5)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>N</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0018036</Xref>
-<Xref>PSI-MOD:00092</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>amidated carboxyl end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__asparagine amide__n">MOD_RES Asparagine amide</Feature>
-</Features>
-<Image src="/images/AA0083.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0083.PDB" />
-</Entry>
-<Entry id="AA0084">
-<Header>
-<Code>AA0084</Code>
-<Dates>
-<CreationDate>22-Nov-1996</CreationDate>
-<StrucRevDate>22-Nov-1996</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-aspartic acid 1-amide</Name>
-<AlternateName>3,4-diamino-4-oxobutanoic acid</AlternateName>
-<AlternateName>3-amino-succinamic acid</AlternateName>
-<AlternateName>alpha-asparagine</AlternateName>
-<AlternateName>isoasparagine</AlternateName>
-<SystematicName>(2S)-2-amino-1-butanediamic acid</SystematicName>
-<Xref>CAS:498-25-9</Xref>
-<Xref>ChEBI:49010</Xref>
-<Xref>PDBHET:NH2</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 7 N 2 O 3</Formula>
-<Weight type="chemical">131.11</Weight>
-<Weight type="physical">131.045667</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0004">
-<Formula>C 0 H 1 N 1 O -1</Formula>
-<Weight type="chemical">-0.98</Weight>
-<Weight type="physical">-0.984016</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kreil, G.</Author>
-<Author>Barra, D.</Author>
-<Author>Simmaco, M.</Author>
-<Author>Erspamer, V.</Author>
-<Author>Erspamer, G.F.</Author>
-<Author>Negri, L.</Author>
-<Author>Severini, C.</Author>
-<Author>Corsi, R.</Author>
-<Author>Melchiorri, P.</Author>
-</Authors>
-<Citation>Eur. J. Pharmacol. 162, 123-128, 1989</Citation>
-<Title>Deltorphin, a novel amphibian skin peptide with high selectivity and affinity for delta opioid receptors.</Title>
-<Xref>DOI:10.1016/0014-2999(89)90611-0</Xref>
-<Xref>PMID:2542051</Xref>
-<Note>chemical synthesis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Regni, C.A.</Author>
-<Author>Roush, R.F.</Author>
-<Author>Miller, D.</Author>
-<Author>Nourse, A.</Author>
-<Author>Walsh, C.T.</Author>
-<Author>Schulman, B.A.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, April 2009</Citation>
-<Description>Crystal structure of E. coli MccB + MccA-N7IsoAsn.</Description>
-<Xref>PDB:3H9G</Xref>
-<Note>X-ray diffraction, 2.20 angstroms</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>peptidylglycine monooxygenase (EC 1.14.17.3)</EnzymeName>
-<EnzymeName>peptidylamidoglycolate lyase (EC 4.3.2.5)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>D</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0018037</Xref>
-<Xref>PSI-MOD:00093</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>amidated carboxyl end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__aspartic acid 1-amide__d">MOD_RES Aspartic acid 1-amide</Feature>
-</Features>
-<Image src="/images/AA0084.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0084.PDB" />
-</Entry>
-<Entry id="AA0085">
-<Header>
-<Code>AA0085</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-cysteine amide</Name>
-<AlternateName>2-amino-3-mercaptopropanamide</AlternateName>
-<AlternateName>cysteinamide</AlternateName>
-<SystematicName>(2R)-2-amino-3-sulfanylpropanamide</SystematicName>
-<Xref>CAS:74401-72-2</Xref>
-<Xref>ChEBI:21262</Xref>
-<Xref>PDBHET:CY3</Xref>
-<Xref>PDBHET:NH2</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 7 N 2 O 1 S 1</Formula>
-<Weight type="chemical">119.16</Weight>
-<Weight type="physical">119.027909</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 0 H 1 N 1 O -1 S 0</Formula>
-<Weight type="chemical">-0.98</Weight>
-<Weight type="physical">-0.984016</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>McIntosh, M.</Author>
-<Author>Cruz, L.J.</Author>
-<Author>Hunkapiller, M.W.</Author>
-<Author>Gray, W.R.</Author>
-<Author>Olivera, B.M.</Author>
-</Authors>
-<Citation>Arch. Biochem. Biophys. 218, 329-334, 1982</Citation>
-<Title>Isolation and structure of a peptide toxin from the marine snail Conus magus.</Title>
-<Xref>DOI:10.1016/0003-9861(82)90351-4</Xref>
-<Xref>PMID:7149738</Xref>
-<Note>chromatographic identification of radioisotope labeled S-carboxymethyl derivative</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Myers, R.A.</Author>
-<Author>Zafaralla, G.C.</Author>
-<Author>Gray, W.R.</Author>
-<Author>Abbott, J.</Author>
-<Author>Cruz, L.J.</Author>
-<Author>Olivera, B.M.</Author>
-</Authors>
-<Citation>Biochemistry 30, 9370-9377, 1991</Citation>
-<Title>alpha-Conotoxins, small peptide probes of nicotinic acetylcholine receptors.</Title>
-<Xref>DOI:10.1021/bi00102a034</Xref>
-<Xref>PMID:1892838</Xref>
-<Note>mass spectrometric detection</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>peptidylglycine monooxygenase (EC 1.14.17.3)</EnzymeName>
-<EnzymeName>peptidylamidoglycolate lyase (EC 4.3.2.5)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0018038</Xref>
-<Xref>PSI-MOD:00094</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>amidated carboxyl end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__cysteine amide__c">MOD_RES Cysteine amide</Feature>
-</Features>
-<Image src="/images/AA0085.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0085.PDB" />
-</Entry>
-<Entry id="AA0086">
-<Header>
-<Code>AA0086</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-glutamine amide</Name>
-<AlternateName>glutaminamide</AlternateName>
-<SystematicName>(2S)-2-aminopentanediamide</SystematicName>
-<Xref>CAS:2013-17-4</Xref>
-<Xref>ChEBI:21309</Xref>
-<Xref>PDBHET:NH2</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 10 N 3 O 2</Formula>
-<Weight type="chemical">144.15</Weight>
-<Weight type="physical">144.077302</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0007">
-<Formula>C 0 H 1 N 1 O -1</Formula>
-<Weight type="chemical">-0.98</Weight>
-<Weight type="physical">-0.984016</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hopkins, C.</Author>
-<Author>Grilley, M.</Author>
-<Author>Miller, C.</Author>
-<Author>Shon, K.J.</Author>
-<Author>Cruz, L.J.</Author>
-<Author>Gray, W.R.</Author>
-<Author>Dykert, J.</Author>
-<Author>Rivier, J.</Author>
-<Author>Yoshikami, D.</Author>
-<Author>Olivera, B.M.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 270, 22361-22367, 1995</Citation>
-<Title>A new family of Conus peptides targeted to the nicotinic acetylcholinereceptor.</Title>
-<Xref>DOI:10.1074/jbc.270.38.22361</Xref>
-<Xref>PMID:7673220</Xref>
-<Note>chemical synthesis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Han, K.H.</Author>
-<Author>Hwang, K.J.</Author>
-<Author>Kim, S.M.</Author>
-<Author>Kim, S.K.</Author>
-<Author>Gray, W.R.</Author>
-<Author>Olivera, B.M.</Author>
-<Author>Rivier, J.</Author>
-<Author>Shon, K.J.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, December 1996</Citation>
-<Description>[Pro7,13] alphaA-conotoxin PIVa, NMR, 12 structures.</Description>
-<Xref>PDB:1P1P</Xref>
-<Note>conformation and disulfide bond assignments by (1)H-NMR</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Han, K.H.</Author>
-<Author>Hwang, K.J.</Author>
-<Author>Kim, S.M.</Author>
-<Author>Kim, S.K.</Author>
-<Author>Gray, W.R.</Author>
-<Author>Olivera, B.M.</Author>
-<Author>Rivier, J.</Author>
-<Author>Shon, K.J.</Author>
-</Authors>
-<Citation>Biochemistry 36, 1669-1677, 1997</Citation>
-<Title>NMR structure determination of a novel conotoxin, [Pro 7,13] alpha A-conotoxin PIVA.</Title>
-<Xref>DOI:10.1021/bi962301k</Xref>
-<Xref>PMID:9048550</Xref>
-<Note>conformation and disulfide bond assignments by (1)H-NMR</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>peptidylglycine monooxygenase (EC 1.14.17.3)</EnzymeName>
-<EnzymeName>peptidylamidoglycolate lyase (EC 4.3.2.5)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>Q</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0018039</Xref>
-<Xref>PSI-MOD:00095</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>amidated carboxyl end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__glutamine amide__q">MOD_RES Glutamine amide</Feature>
-</Features>
-<Image src="/images/AA0086.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0086.PDB" />
-</Entry>
-<Entry id="AA0087">
-<Header>
-<Code>AA0087</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-glutamic acid 1-amide</Name>
-<AlternateName>4,5-diamino-5-oxopentanoic acid</AlternateName>
-<AlternateName>isoglutamine</AlternateName>
-<SystematicName>(2S)-2-amino-1-pentanediamic acid</SystematicName>
-<Xref>CAS:328-48-3</Xref>
-<Xref>ChEBI:21305</Xref>
-<Xref>PDBHET:NH2</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 9 N 2 O 3</Formula>
-<Weight type="chemical">145.14</Weight>
-<Weight type="physical">145.061317</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0006">
-<Formula>C 0 H 1 N 1 O -1</Formula>
-<Weight type="chemical">-0.98</Weight>
-<Weight type="physical">-0.984016</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kreil, G.</Author>
-</Authors>
-<Citation>FEBS Lett. 54, 100-102, 1975</Citation>
-<Title>The structure of Apis dorsata melittin: phylogenetic relationships between honeybees as deduced from sequence data.</Title>
-<Xref>DOI:10.1016/0014-5793(75)81079-9</Xref>
-<Xref>PMID:1093875</Xref>
-<Note>chromatographic identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sudarslal, S.</Author>
-<Author>Majumdar, S.</Author>
-<Author>Ramasamy, P.</Author>
-<Author>Dhawan, R.</Author>
-<Author>Pal, P.P.</Author>
-<Author>Ramaswami, M.</Author>
-<Author>Lala, A.K.</Author>
-<Author>Sikdar, S.K.</Author>
-<Author>Sarma, S.P.</Author>
-<Author>Krishnan, K.S.</Author>
-<Author>Balaram, P.</Author>
-</Authors>
-<Citation>FEBS Lett. 553, 209-212, 2003</Citation>
-<Title>Sodium channel modulating activity in a delta-conotoxin from an Indian marine snail.</Title>
-<Xref>DOI:10.1016/S0014-5793(03)01016-0</Xref>
-<Xref>PMID:14550575</Xref>
-<Note>mass spectrometric detection</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>peptidylglycine monooxygenase (EC 1.14.17.3)</EnzymeName>
-<EnzymeName>peptidylamidoglycolate lyase (EC 4.3.2.5)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>E</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0018040</Xref>
-<Xref>PSI-MOD:00096</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>amidated carboxyl end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__glutamic acid 1-amide__e">MOD_RES Glutamic acid 1-amide</Feature>
-</Features>
-<Image src="/images/AA0087.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0087.PDB" />
-</Entry>
-<Entry id="AA0088">
-<Header>
-<Code>AA0088</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>glycine amide</Name>
-<AlternateName>2-aminoacetamide</AlternateName>
-<AlternateName>2-azanylethanamide</AlternateName>
-<AlternateName>glycinamide</AlternateName>
-<SystematicName>2-aminoethanamide</SystematicName>
-<Xref>CAS:598-41-4</Xref>
-<Xref>ChEBI:42843</Xref>
-<Xref>PDBHET:NH2</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 2 H 5 N 2 O 1</Formula>
-<Weight type="chemical">73.07</Weight>
-<Weight type="physical">73.040188</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0008">
-<Formula>C 0 H 1 N 1 O -1</Formula>
-<Weight type="chemical">-0.98</Weight>
-<Weight type="physical">-0.984016</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Light, A.</Author>
-<Author>du Vigneaud, V.</Author>
-</Authors>
-<Citation>Proc. Soc. Exp. Biol. Med. 98, 692-696, 1958</Citation>
-<Title>On the nature of oxytocin and vasopressin from human pituitary.</Title>
-<Xref>PMID:13591312</Xref>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>peptidylglycine monooxygenase (EC 1.14.17.3)</EnzymeName>
-<EnzymeName>peptidylamidoglycolate lyase (EC 4.3.2.5)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>G</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0018041</Xref>
-<Xref>PSI-MOD:00097</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>amidated carboxyl end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__glycine amide__g">MOD_RES Glycine amide</Feature>
-</Features>
-<Image src="/images/AA0088.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0088.PDB" />
-</Entry>
-<Entry id="AA0089">
-<Header>
-<Code>AA0089</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-histidine amide</Name>
-<AlternateName>histidinamide</AlternateName>
-<SystematicName>(2S)-2-amino-3-(1H-imidazol-4-yl)propanamide</SystematicName>
-<Xref>CAS:7621-14-9</Xref>
-<Xref>ChEBI:43042</Xref>
-<Xref>PDBHET:HIA</Xref>
-<Xref>PDBHET:NH2</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 9 N 4 O 1</Formula>
-<Weight type="chemical">153.16</Weight>
-<Weight type="physical">153.077636</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0009">
-<Formula>C 0 H 1 N 1 O -1</Formula>
-<Weight type="chemical">-0.98</Weight>
-<Weight type="physical">-0.984016</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Chicchi, G.G.</Author>
-<Author>Gimenez-Gallego, G.</Author>
-<Author>Ber, E.</Author>
-<Author>Garcia, M.L.</Author>
-<Author>Winquist, R.</Author>
-<Author>Cascieri, M.A.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 263, 10192-10197, 1988</Citation>
-<Title>Purification and characterization of a unique, potent inhibitor of apamin binding from Leiurus quinquestriatus hebraeus venom.</Title>
-<Xref>PMID:2839478</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Auguste, P.</Author>
-<Author>Hugues, M.</Author>
-<Author>Grave, B.</Author>
-<Author>Gesquiere, J.C.</Author>
-<Author>Maes, P.</Author>
-<Author>Tartar, A.</Author>
-<Author>Romey, G.</Author>
-<Author>Schweitz, H.</Author>
-<Author>Lazdunski, M.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 265, 4753-4759, 1990</Citation>
-<Title>Leiurotoxin I (scyllatoxin), a peptide ligand for Ca2(+)-activated K+ channels. Chemical synthesis, radiolabeling, and receptor characterization.</Title>
-<Xref>PMID:2307683</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Martins, J.C.</Author>
-<Author>Zhang, W.G.</Author>
-<Author>Tartar, A.</Author>
-<Author>Lazdunski, M.</Author>
-<Author>Borremans, F.A.</Author>
-</Authors>
-<Citation>FEBS Lett. 260, 249-253, 1990</Citation>
-<Title>Solution conformation of leiurotoxin I (scyllatoxin) by 1H nuclear magnetic resonance. Resonance assignment and secondary structure.</Title>
-<Xref>DOI:10.1016/0014-5793(90)80115-Y</Xref>
-<Xref>PMID:2153586</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Martins, J.C.</Author>
-<Author>van de Ven, F.J.M.</Author>
-<Author>Borremans, F.A.M.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, June 1994</Citation>
-<Description>Determination of the three-dimensional solution structure of scyllatoxin by 1H nuclear magnetic resonance.</Description>
-<Xref>PDB:1SCY</Xref>
-<Note>(1)H-NMR characterization</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>peptidylglycine monooxygenase (EC 1.14.17.3)</EnzymeName>
-<EnzymeName>peptidylamidoglycolate lyase (EC 4.3.2.5)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>H</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0018042</Xref>
-<Xref>PSI-MOD:00098</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>amidated carboxyl end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__histidine amide__h">MOD_RES Histidine amide</Feature>
-</Features>
-<Image src="/images/AA0089.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0089.PDB" />
-</Entry>
-<Entry id="AA0090">
-<Header>
-<Code>AA0090</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-isoleucine amide</Name>
-<AlternateName>isoleucinamide</AlternateName>
-<SystematicName>(2S,3S)-2-amino-3-methylpentanamide</SystematicName>
-<Xref>CAS:14445-54-6</Xref>
-<Xref>ChEBI:21345</Xref>
-<Xref>PDBHET:NH2</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 13 N 2 O 1</Formula>
-<Weight type="chemical">129.18</Weight>
-<Weight type="physical">129.102788</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0010">
-<Formula>C 0 H 1 N 1 O -1</Formula>
-<Weight type="chemical">-0.98</Weight>
-<Weight type="physical">-0.984016</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Teshima, T.</Author>
-<Author>Ueki, Y.</Author>
-<Author>Nakai, T.</Author>
-<Author>Shiba, T.</Author>
-</Authors>
-<Citation>Tetrahedron 42, 829-834, 1986</Citation>
-<Title>Structure determination of lepidopteran, self-defense substance produced by silkworm.</Title>
-<Xref>DOI:10.1016/S0040-4020(01)87488-3</Xref>
-<Note>chromatographic detection; chemical synthesis</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>peptidylglycine monooxygenase (EC 1.14.17.3)</EnzymeName>
-<EnzymeName>peptidylamidoglycolate lyase (EC 4.3.2.5)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>I</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0018043</Xref>
-<Xref>PSI-MOD:00099</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>amidated carboxyl end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__isoleucine amide__i">MOD_RES Isoleucine amide</Feature>
-</Features>
-<Image src="/images/AA0090.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0090.PDB" />
-</Entry>
-<Entry id="AA0091">
-<Header>
-<Code>AA0091</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-leucine amide</Name>
-<AlternateName>2-amino-4-methylvaleramide</AlternateName>
-<AlternateName>2-azanyl-4-methylpentanamide</AlternateName>
-<AlternateName>alpha-aminoisocaproamide</AlternateName>
-<AlternateName>leucinamide</AlternateName>
-<SystematicName>(2S)-2-amino-4-methylpentanamide</SystematicName>
-<Xref>CAS:687-51-4</Xref>
-<Xref>ChEBI:21349</Xref>
-<Xref>PDBHET:NH2</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 13 N 2 O 1</Formula>
-<Weight type="chemical">129.18</Weight>
-<Weight type="physical">129.102788</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0011">
-<Formula>C 0 H 1 N 1 O -1</Formula>
-<Weight type="chemical">-0.98</Weight>
-<Weight type="physical">-0.984016</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Argiolas, A.</Author>
-<Author>Pisano, J.J.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 260, 1437-1444, 1985</Citation>
-<Title>Bombolitins, a new class of mast cell degranulating peptides from the venom of the bumblebee Megabombus pennsylvanicus.</Title>
-<Xref>PMID:2578459</Xref>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>peptidylglycine monooxygenase (EC 1.14.17.3)</EnzymeName>
-<EnzymeName>peptidylamidoglycolate lyase (EC 4.3.2.5)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>L</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0018044</Xref>
-<Xref>PSI-MOD:00100</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>amidated carboxyl end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__leucine amide__l">MOD_RES Leucine amide</Feature>
-</Features>
-<Image src="/images/AA0091.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0091.PDB" />
-</Entry>
-<Entry id="AA0092">
-<Header>
-<Code>AA0092</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-lysine amide</Name>
-<AlternateName>lysinamide</AlternateName>
-<SystematicName>(2S)-2,6-diaminohexanamide</SystematicName>
-<Xref>CAS:32388-19-5</Xref>
-<Xref>ChEBI:21353</Xref>
-<Xref>PDBHET:NH2</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 14 N 3 O 1</Formula>
-<Weight type="chemical">144.20</Weight>
-<Weight type="physical">144.113687</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 0 H 1 N 1 O -1</Formula>
-<Weight type="chemical">-0.98</Weight>
-<Weight type="physical">-0.984016</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Andreu, D.</Author>
-<Author>Merrifield, R.B.</Author>
-<Author>Steiner, H.</Author>
-<Author>Boman, H.G.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 80, 6475-6479, 1983</Citation>
-<Title>Solid-phase synthesis of cecropin A and related peptides.</Title>
-<Xref>DOI:10.1073/pnas.80.21.6475</Xref>
-<Xref>PMID:6579533</Xref>
-<Note>mass spectrometric identification; chemical synthesis</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>peptidylglycine monooxygenase (EC 1.14.17.3)</EnzymeName>
-<EnzymeName>peptidylamidoglycolate lyase (EC 4.3.2.5)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0018045</Xref>
-<Xref>PSI-MOD:00101</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>amidated carboxyl end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__lysine amide__k">MOD_RES Lysine amide</Feature>
-</Features>
-<Image src="/images/AA0092.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0092.PDB" />
-</Entry>
-<Entry id="AA0093">
-<Header>
-<Code>AA0093</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-methionine amide</Name>
-<AlternateName>2-amino-4-(methylthio)butanamide</AlternateName>
-<AlternateName>methioninamide</AlternateName>
-<SystematicName>(2S)-2-amino-4-(methylsulfanyl)butanamide</SystematicName>
-<Xref>CAS:4510-08-1</Xref>
-<Xref>ChEBI:21362</Xref>
-<Xref>PDBHET:NH2</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 11 N 2 O 1 S 1</Formula>
-<Weight type="chemical">147.22</Weight>
-<Weight type="physical">147.059209</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0013">
-<Formula>C 0 H 1 N 1 O -1 S 0</Formula>
-<Weight type="chemical">-0.98</Weight>
-<Weight type="physical">-0.984016</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lowry, P.J.</Author>
-<Author>Bennett, H.P.</Author>
-<Author>McMartin, C.</Author>
-</Authors>
-<Citation>Biochem. J. 141, 427-437, 1974</Citation>
-<Title>The isolation and amino acid sequence of an adrenocorticotrophin from the pars distalis and a corticotrophin-like intermediate-lobe peptide from the neurointermediate lobe of the pituitary of the dogfish Squalus acanthias.</Title>
-<Xref>PMID:4375977</Xref>
-</ReferenceBlock>
-<Comment>Although appropriate, the keyword "thioether bond" normally does not appear for this amino acid.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptidylglycine monooxygenase (EC 1.14.17.3)</EnzymeName>
-<EnzymeName>peptidylamidoglycolate lyase (EC 4.3.2.5)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>M</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0018046</Xref>
-<Xref>PSI-MOD:00102</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>*thioether bond</Keyword>
-<Keyword>amidated carboxyl end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__methionine amide__m">MOD_RES Methionine amide</Feature>
-</Features>
-<Image src="/images/AA0093.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0093.PDB" />
-</Entry>
-<Entry id="AA0094">
-<Header>
-<Code>AA0094</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-phenylalanine amide</Name>
-<AlternateName>phenylalaninamide</AlternateName>
-<SystematicName>(2S)-2-amino-3-phenylpropanamide</SystematicName>
-<Xref>CAS:5241-58-7</Xref>
-<Xref>ChEBI:21371</Xref>
-<Xref>PDBHET:NFA</Xref>
-<Xref>PDBHET:NH2</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 11 N 2 O 1</Formula>
-<Weight type="chemical">163.20</Weight>
-<Weight type="physical">163.087138</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0014">
-<Formula>C 0 H 1 N 1 O -1</Formula>
-<Weight type="chemical">-0.98</Weight>
-<Weight type="physical">-0.984016</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Grimmelikhuijzen, C.J.P.</Author>
-<Author>Hahn, M.</Author>
-<Author>Rinehart, K.L.</Author>
-<Author>Spencer, A.N.</Author>
-</Authors>
-<Citation>Brain Res. 475, 198-203, 1988</Citation>
-<Title>Isolation of &lt;Glu-Leu-Leu-Gly-Gly-Arg-Phe-NH-2(Pol-RFamide), a novel neuropeptide from hydromedusae.</Title>
-<Xref>DOI:10.1016/0006-8993(88)90219-3</Xref>
-<Xref>PMID:2905621</Xref>
-<Note>chromatographic and radioimmunoassay identification; chemical synthesis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Nakamura, T.</Author>
-<Author>Yu, Z.</Author>
-<Author>Fainzilber, M.</Author>
-<Author>Burlingame, A.L.</Author>
-</Authors>
-<Citation>Protein Sci. 5, 524-530, 1996</Citation>
-<Title>Mass spectrometric-based revision of the structure of a cysteine-rich peptide toxin with gamma-carboxyglutamic acid, TxVIIA, from the sea snail, Conus textile.</Title>
-<Xref>DOI:10.1002/pro.5560050315</Xref>
-<Xref>PMID:8868490</Xref>
-<Note>mass spectrometric identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Remington, S.J.</Author>
-<Author>Wachter, R.M.</Author>
-<Author>Yarbrough, D.K.</Author>
-<Author>Branchaud, B.</Author>
-<Author>Anderson, D.C.</Author>
-<Author>Kallio, K.</Author>
-<Author>Lukyanov, K.A.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, August 2004</Citation>
-<Description>Crystal Structure of Wild Type Yellow Fluorescent Protein zFP538 from Zoanthus.</Description>
-<Xref>PDB:1XAE</Xref>
-<Note>X-ray diffraction, 2.70 angstroms; this amide is produced by an autolytic process</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>peptidylglycine monooxygenase (EC 1.14.17.3)</EnzymeName>
-<EnzymeName>peptidylamidoglycolate lyase (EC 4.3.2.5)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>F</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0018047</Xref>
-<Xref>PSI-MOD:00103</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>amidated carboxyl end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__phenylalanine amide__f">MOD_RES Phenylalanine amide</Feature>
-</Features>
-<Image src="/images/AA0094.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0094.PDB" />
-</Entry>
-<Entry id="AA0095">
-<Header>
-<Code>AA0095</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-proline amide</Name>
-<AlternateName>prolinamide</AlternateName>
-<SystematicName>(2S)-pyrrolidine-2-carboxamide</SystematicName>
-<Xref>CAS:7531-52-4</Xref>
-<Xref>ChEBI:21374</Xref>
-<Xref>PDBHET:NH2</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 9 N 2 O 1</Formula>
-<Weight type="chemical">113.14</Weight>
-<Weight type="physical">113.071488</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0015">
-<Formula>C 0 H 1 N 1 O -1</Formula>
-<Weight type="chemical">-0.98</Weight>
-<Weight type="physical">-0.984016</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Neher, R.</Author>
-<Author>Riniker, B.</Author>
-<Author>Rittel, W.</Author>
-<Author>Zuber, H.</Author>
-</Authors>
-<Citation>Helv. Chim. Acta 51, 1900-1905, 1968</Citation>
-<Title>Menschliches calcitonin. III. Struktur von calcitonin M und D.</Title>
-<Xref>DOI:10.1002/hlca.19680510811</Xref>
-<Xref>PMID:5760861</Xref>
-<Note>chemical identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bøler, J.</Author>
-<Author>Enzmann, F.</Author>
-<Author>Folkers, K.</Author>
-<Author>Bowers, C.Y.</Author>
-<Author>Schally, A.V.</Author>
-</Authors>
-<Citation>Biochem. Biophys. Res. Commun. 37, 705-710, 1969</Citation>
-<Title>The identity of chemical and hormonal properties of the thyrotropin releasing hormone and pyroglutamyl-histidyl-proline amide.</Title>
-<Xref>DOI:10.1016/0006-291X(69)90868-7</Xref>
-<Xref>PMID:4982117</Xref>
-<Note>chemical synthesis; the spelling of "Boler, J." in the PubMed citation is corrected</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>peptidylglycine monooxygenase (EC 1.14.17.3)</EnzymeName>
-<EnzymeName>peptidylamidoglycolate lyase (EC 4.3.2.5)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>P</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0018048</Xref>
-<Xref>PSI-MOD:00104</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>amidated carboxyl end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__proline amide__p">MOD_RES Proline amide</Feature>
-</Features>
-<Image src="/images/AA0095.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0095.PDB" />
-</Entry>
-<Entry id="AA0096">
-<Header>
-<Code>AA0096</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-serine amide</Name>
-<AlternateName>serinamide</AlternateName>
-<SystematicName>(2S)-2-amino-3-hydroxypropanamide</SystematicName>
-<Xref>CAS:6791-49-7</Xref>
-<Xref>ChEBI:21389</Xref>
-<Xref>PDBHET:NH2</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 7 N 2 O 2</Formula>
-<Weight type="chemical">103.10</Weight>
-<Weight type="physical">103.050752</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 0 H 1 N 1 O -1</Formula>
-<Weight type="chemical">-0.98</Weight>
-<Weight type="physical">-0.984016</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Maeda, N.</Author>
-<Author>Tamiya, N.</Author>
-</Authors>
-<Citation>Biochem. J. 175, 507-517, 1978</Citation>
-<Title>Three neurotoxins from the venom of a sea snake Astrotia stokesii, including two long-chain neurotoxic proteins with amidated C-termini.</Title>
-<Xref>PMID:743209</Xref>
-<Note>chromatographic identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yu, Y.</Author>
-<Author>Guo, H.</Author>
-<Author>Zhang, Q.</Author>
-<Author>Duan, L.</Author>
-<Author>Ding, Y.</Author>
-<Author>Liao, R.</Author>
-<Author>Lei, C.</Author>
-<Author>Shen, B.</Author>
-<Author>Liu, W.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 132, 16324-16326, 2010</Citation>
-<Title>NosA Catalyzing Carboxyl-Terminal Amide Formation in Nosiheptide Maturation via an Enamine Dealkylation on the Serine-Extended Precursor Peptide.</Title>
-<Xref>DOI:10.1021/ja106571g</Xref>
-<Xref>PMID:21047073</Xref>
-<Note>serine amide in a bacterial antibiotic is formed by oxidative cleavage of a terminal serine residue</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>peptidylglycine monooxygenase (EC 1.14.17.3)</EnzymeName>
-<EnzymeName>peptidylamidoglycolate lyase (EC 4.3.2.5)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0018049</Xref>
-<Xref>PSI-MOD:00105</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>amidated carboxyl end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__serine amide__s">MOD_RES Serine amide</Feature>
-</Features>
-<Image src="/images/AA0096.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0096.PDB" />
-</Entry>
-<Entry id="AA0097">
-<Header>
-<Code>AA0097</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-threonine amide</Name>
-<AlternateName>threoninamide</AlternateName>
-<SystematicName>(2S,3R)-2-amino-3-hydroxybutanamide</SystematicName>
-<Xref>CAS:2280-40-2</Xref>
-<Xref>ChEBI:21404</Xref>
-<Xref>PDBHET:NH2</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 9 N 2 O 2</Formula>
-<Weight type="chemical">117.13</Weight>
-<Weight type="physical">117.066403</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0017">
-<Formula>C 0 H 1 N 1 O -1</Formula>
-<Weight type="chemical">-0.98</Weight>
-<Weight type="physical">-0.984016</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ramilo, C.A.</Author>
-<Author>Zafaralla, G.C.</Author>
-<Author>Nadasdi, L.</Author>
-<Author>Hammerland, L.G.</Author>
-<Author>Yoshikami, D.</Author>
-<Author>Gray, W.R.</Author>
-<Author>Kristipati, R.</Author>
-<Author>Ramachandran, J.</Author>
-<Author>Miljanich, G.</Author>
-<Author>Olivera, B.M.</Author>
-</Authors>
-<Citation>Biochemistry 31, 9919-9926, 1992</Citation>
-<Title>Novel alpha- and omega-conotoxins from Conus striatus venom.</Title>
-<Xref>DOI:10.1021/bi00156a009</Xref>
-<Xref>PMID:1390774</Xref>
-<Note>chemical synthesis</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>peptidylglycine monooxygenase (EC 1.14.17.3)</EnzymeName>
-<EnzymeName>peptidylamidoglycolate lyase (EC 4.3.2.5)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>T</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0018050</Xref>
-<Xref>PSI-MOD:00106</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>amidated carboxyl end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__threonine amide__t">MOD_RES Threonine amide</Feature>
-</Features>
-<Image src="/images/AA0097.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0097.PDB" />
-</Entry>
-<Entry id="AA0098">
-<Header>
-<Code>AA0098</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-tryptophan amide</Name>
-<AlternateName>tryptophanamide</AlternateName>
-<SystematicName>(2S)-2-amino-3-(1H-indol-3-yl)propanamide</SystematicName>
-<Xref>CAS:20696-57-5</Xref>
-<Xref>ChEBI:16533</Xref>
-<Xref>PDBHET:NH2</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 11 H 12 N 3 O 1</Formula>
-<Weight type="chemical">202.24</Weight>
-<Weight type="physical">202.098037</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0018">
-<Formula>C 0 H 1 N 1 O -1</Formula>
-<Weight type="chemical">-0.98</Weight>
-<Weight type="physical">-0.984016</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gäde, G.</Author>
-<Author>Goldsworthy, G.J.</Author>
-<Author>Schaffer, M.H.</Author>
-<Author>Cook, J.C.</Author>
-<Author>Rinehart Jr., K.L.</Author>
-</Authors>
-<Citation>Biochem. Biophys. Res. Commun. 134, 723-730, 1986</Citation>
-<Title>Sequence analyses of adipokinetic hormones II from corpora cardiaca of Schistocerca nitans, Schistocerca gregaria, and Locusta migratoria by fast atom bombardment mass spectrometry.</Title>
-<Xref>DOI:10.1016/S0006-291X(86)80480-6</Xref>
-<Xref>PMID:3947348</Xref>
-<Note>mass spectrometric identification</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>peptidylglycine monooxygenase (EC 1.14.17.3)</EnzymeName>
-<EnzymeName>peptidylamidoglycolate lyase (EC 4.3.2.5)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>W</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0018051</Xref>
-<Xref>PSI-MOD:00107</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>amidated carboxyl end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__tryptophan amide__w">MOD_RES Tryptophan amide</Feature>
-</Features>
-<Image src="/images/AA0098.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0098.PDB" />
-</Entry>
-<Entry id="AA0099">
-<Header>
-<Code>AA0099</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-tyrosine amide</Name>
-<AlternateName>tyrosinamide</AlternateName>
-<SystematicName>(2S)-2-amino-3-(4-hydoxyphenyl)propanamide</SystematicName>
-<Xref>CAS:4985-46-0</Xref>
-<Xref>ChEBI:21412</Xref>
-<Xref>PDBHET:NH2</Xref>
-<Xref>PDBHET:TYC</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 11 N 2 O 2</Formula>
-<Weight type="chemical">179.20</Weight>
-<Weight type="physical">179.082053</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0019">
-<Formula>C 0 H 1 N 1 O -1</Formula>
-<Weight type="chemical">-0.98</Weight>
-<Weight type="physical">-0.984016</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Olivera, B.M.</Author>
-<Author>McIntosh, J.M.</Author>
-<Author>Cruz, L.J.</Author>
-<Author>Luque, F.A.</Author>
-<Author>Gray, W.R.</Author>
-</Authors>
-<Citation>Biochemistry 23, 5087-5090, 1984</Citation>
-<Title>Purification and sequence of a presynaptic peptide toxin from Conus geographus venom.</Title>
-<Xref>DOI:10.1021/bi00317a001</Xref>
-<Xref>PMID:6509012</Xref>
-<Note>chromatographic identification of PTC derivative</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Conlon, J.M.</Author>
-<Author>Schmidt, W.E.</Author>
-<Author>Gallwitz, B.</Author>
-<Author>Falkmer, S.</Author>
-<Author>Thim, L.</Author>
-</Authors>
-<Citation>Regul. Pept. 16, 261-268, 1986</Citation>
-<Title>Characterization of an amidated form of pancreatic polypeptide from the daddy sculpin (Cottus scorpius).</Title>
-<Xref>DOI:10.1016/0167-0115(86)90025-X</Xref>
-<Xref>PMID:3562898</Xref>
-<Note>mass spectrometric characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Takamatsu, K.</Author>
-<Author>Tatemoto, K.</Author>
-</Authors>
-<Citation>Neurochem. Res. 17, 239-246, 1992</Citation>
-<Title>Isolation and characterization of two novel peptide amides originating from myelin basic protein in bovine brain.</Title>
-<Xref>DOI:10.1007/BF00966665</Xref>
-<Xref>PMID:1377792</Xref>
-<Note>this peptide has a carboxyl-terminal amide probably produced by a non-enzymatic reaction</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>peptidylglycine monooxygenase (EC 1.14.17.3)</EnzymeName>
-<EnzymeName>peptidylamidoglycolate lyase (EC 4.3.2.5)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>Y</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0018052</Xref>
-<Xref>PSI-MOD:00108</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>amidated carboxyl end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__tyrosine amide__y">MOD_RES Tyrosine amide</Feature>
-</Features>
-<Image src="/images/AA0099.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0099.PDB" />
-</Entry>
-<Entry id="AA0100">
-<Header>
-<Code>AA0100</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-valine amide</Name>
-<AlternateName>valinamide</AlternateName>
-<SystematicName>(2S)-2-amino-3-methylbutanamide</SystematicName>
-<Xref>CAS:4540-60-7</Xref>
-<Xref>ChEBI:21418</Xref>
-<Xref>PDBHET:NH2</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 11 N 2 O 1</Formula>
-<Weight type="chemical">115.16</Weight>
-<Weight type="physical">115.087138</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0020">
-<Formula>C 0 H 1 N 1 O -1</Formula>
-<Weight type="chemical">-0.98</Weight>
-<Weight type="physical">-0.984016</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mutt, V.</Author>
-<Author>Jorpes, J.E.</Author>
-<Author>Magnusson, S.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 15, 513-519, 1970</Citation>
-<Title>Structure of porcine secretin. The amino acid sequence.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1970.tb01034.x</Xref>
-<Xref>PMID:5465996</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Argiolas, A.</Author>
-<Author>Pisano, J.J.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 260, 1437-1444, 1985</Citation>
-<Title>Bombolitins, a new class of mast cell degranulating peptides from the venom of the bumblebee Megabombus pennsylvanicus.</Title>
-<Xref>PMID:2578459</Xref>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>peptidylglycine monooxygenase (EC 1.14.17.3)</EnzymeName>
-<EnzymeName>peptidylamidoglycolate lyase (EC 4.3.2.5)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>V</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0018053</Xref>
-<Xref>PSI-MOD:00109</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>amidated carboxyl end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__valine amide__v">MOD_RES Valine amide</Feature>
-</Features>
-<Image src="/images/AA0100.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0100.PDB" />
-</Entry>
-<Entry id="AA0101">
-<Header>
-<Code>AA0101</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Jun-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-cysteine methyl disulfide</Name>
-<AlternateName>2-amino-3-(methyldisulfanediyl)propanoic acid</AlternateName>
-<AlternateName>2-amino-3-(methyldithio)propanoic acid</AlternateName>
-<AlternateName>2-amino-3-methyldisulfanylpropanoic acid</AlternateName>
-<AlternateName>2-azanyl-3-(methyldisulfanediyl)-propanoic acid</AlternateName>
-<AlternateName>L-3-(methyldithio)alanine</AlternateName>
-<AlternateName>S-methylthio-L-cysteine</AlternateName>
-<AlternateName>S-methylthiocysteine</AlternateName>
-<SystematicName>(2R)-2-amino-3-(methyldisulfanediyl)propanoic acid</SystematicName>
-<Xref>CAS:33784-54-2</Xref>
-<Xref>PDBHET:SCH</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 7 N 1 O 1 S 2</Formula>
-<Weight type="chemical">149.23</Weight>
-<Weight type="physical">148.996906</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 1 H 2 N 0 O 0 S 1</Formula>
-<Weight type="chemical">46.09</Weight>
-<Weight type="physical">45.987721</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lo, S.S.</Author>
-<Author>Fraser, B.A.</Author>
-<Author>Liu, T.Y.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 259, 11041-11045, 1984</Citation>
-<Title>The mixed disulfide in the zymogen of streptococcal proteinase. Characterization and implication for its biosynthesis.</Title>
-<Xref>PMID:6381494</Xref>
-<Note>mass spectrometric detection; isotope labeling</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kissinger, C.R.</Author>
-<Author>Sieker, L.C.</Author>
-<Author>Adman, E.T.</Author>
-<Author>Jensen, L.H.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 219, 693-715, 1991</Citation>
-<Title>Refined crystal structure of ferredoxin II from Desulfovibrio gigas at 1.7 A.</Title>
-<Xref>DOI:10.1016/0022-2836(91)90665-S</Xref>
-<Xref>PMID:2056535</Xref>
-<Note>X-ray diffraction, 1.7 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kissinger, C.R.</Author>
-<Author>Sieker, L.C.</Author>
-<Author>Adman, E.T.</Author>
-<Author>Jensen, L.H.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, April 1991</Citation>
-<Description>Refined crystal structure of ferredoxin II from Desulfovibrio gigas at 1.7 A.</Description>
-<Xref>PDB:1FXD</Xref>
-<Note>X-ray diffraction, 1.70 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Goodfellow, B.J.</Author>
-<Author>Macedo, A.L.</Author>
-<Author>Rodrigues, P.</Author>
-<Author>Moura, I.</Author>
-<Author>Wray, V.</Author>
-<Author>Moura, J.J.</Author>
-</Authors>
-<Citation>J. Biol. Inorg. Chem. 4, 421-430, 1999</Citation>
-<Title>The solution structure of a [3Fe-4S] ferredoxin: oxidised ferredoxin II from Desulfovibrio gigas.</Title>
-<Xref>DOI:10.1007/s007750050328</Xref>
-<Xref>PMID:10555576</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Goodfellow, B.J.</Author>
-<Author>Macedo, A.L.</Author>
-<Author>Rodrigues, P.</Author>
-<Author>Wray, V.</Author>
-<Author>Moura, I.</Author>
-<Author>Moura, J.J.G.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, October 1998</Citation>
-<Description>The NMR solution structure of the 3Fe ferredoxin II from Desulfovibrio gigas, 15 structures.</Description>
-<Xref>PDB:1F2G</Xref>
-<Note>COSY, TOCSY, and NOESY NMR spectroscopy; the cysteine methyl disulfide modification is not reported for this structure</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>GO:0018222</Xref>
-<Xref>PSI-MOD:00110</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>disulfide bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__cysteine methyl disulfide__c">MOD_RES Cysteine methyl disulfide</Feature>
-</Features>
-<Image src="/images/AA0101.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0101.PDB" />
-</Entry>
-<Entry id="AA0102">
-<Header>
-<Code>AA0102</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-farnesyl-L-cysteine</Name>
-<AlternateName>2-amino-3-(3,7,11-trimethyl-2,6,10-dodecatrienylthio)propanoic acid</AlternateName>
-<SystematicName>(2R)-2-amino-3-([(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]sulfanyl)propanoic acid</SystematicName>
-<Xref>CAS:68000-92-0</Xref>
-<Xref>ChEBI:86019</Xref>
-<Xref>PDBHET:FAR</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 18 H 29 N 1 O 1 S 1</Formula>
-<Weight type="chemical">307.50</Weight>
-<Weight type="physical">307.196986</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 15 H 24 N 0 O 0 S 0</Formula>
-<Weight type="chemical">204.36</Weight>
-<Weight type="physical">204.187801</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Farnsworth, C.C.</Author>
-<Author>Wolda, S.L.</Author>
-<Author>Gelb, M.H.</Author>
-<Author>Glomset, J.A.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 264, 20422-20429, 1989</Citation>
-<Title>Human lamin B contains a farnesylated cysteine residue.</Title>
-<Xref>PMID:2684976</Xref>
-<Note>radiolabeling; mass spectrometric and chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Tuinman, A.A.</Author>
-<Author>Thomas, D.A.</Author>
-<Author>Cook, K.D.</Author>
-<Author>Xue, C.B.</Author>
-<Author>Naider, F.</Author>
-<Author>Becker, J.M.</Author>
-</Authors>
-<Citation>Anal. Biochem. 193, 173-177, 1991</Citation>
-<Title>Mass spectrometric signature of S-prenylated cysteine peptides.</Title>
-<Xref>DOI:10.1016/0003-2697(91)90004-D</Xref>
-<Xref>PMID:1872463</Xref>
-<Note>mass spectrometric identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Heilmeyer Jr., L.M.G.</Author>
-<Author>Serwe, M.</Author>
-<Author>Weber, C.</Author>
-<Author>Metzger, J.</Author>
-<Author>Hoffmann-Posorske, E.</Author>
-<Author>Meyer, H.E.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 89, 9554-9558, 1992</Citation>
-<Title>Farnesylcysteine, a constituent of the alpha and beta subunits of rabbit skeletal muscle phosphorylase kinase: localization by conversion to S-ethylcysteine and by tandem mass spectrometry.</Title>
-<Xref>DOI:10.1073/pnas.89.20.9554</Xref>
-<Xref>PMID:1409665</Xref>
-<Note>farnesylation not followed by cleavage of the terminal peptide and methylation of the new carboxyl end</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Long, S.B.</Author>
-<Author>Casey, P.J.</Author>
-<Author>Beese, L.S.</Author>
-</Authors>
-<Citation>Nature 419, 645-650, 2002</Citation>
-<Title>Reaction path of protein farnesyltransferase at atomic resolution.</Title>
-<Xref>DOI:10.1038/nature00986</Xref>
-<Xref>PMID:12374986</Xref>
-<Note>X-ray diffraction, 2.10 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Long, S.B.</Author>
-<Author>Casey, P.J.</Author>
-<Author>Beese, L.S.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, February 2002</Citation>
-<Description>Protein farnesyltransferase complexed with a farnesylated K-Ras4B peptide product.</Description>
-<Xref>PDB:1KZP</Xref>
-<Note>X-ray diffraction, 2.10 angstroms</Note>
-</ReferenceBlock>
-<Comment>Formation of S-farnesycysteine may be coupled with subsequent cleavage of a carboxy-terminal tripeptide for the CXXX motif and methyl esterification of the farnesylated cysteine. See L-cysteine methyl ester (RESID:AA0105).</Comment>
-<Comment>This modification may be found at the first position in the sequence motif CXX[SAQCMT]* where the second and third positions are usually aliphatic.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>protein farnesyltransferase</EnzymeName>
-<EnzymeName>farnesyl-diphosphate:protein-cysteine farnesyltransferase (EC 2.5.1.58)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Condition>incidental to RESID:AA0105</Condition>
-<Xref>GO:0018226</Xref>
-<Xref>PSI-MOD:00111</Xref>
-<Xref>PSI-MOD:01116</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lipoprotein</Keyword>
-<Keyword>prenylation</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__s-farnesyl cysteine__c">LIPID S-farnesyl cysteine</Feature>
-</Features>
-<Image src="/images/AA0102.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0102.PDB" />
-</Entry>
-<Entry id="AA0103">
-<Header>
-<Code>AA0103</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Sep-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-12-hydroxyfarnesyl-L-cysteine</Name>
-<AlternateName>2-amino-3-(12-hydroxy-3,7,11-trimethyl-3,6,10-dodecatrienylthio)propanoic acid</AlternateName>
-<SystematicName>(2R)-2-amino-3-([(2E,6E,10Z)-12-hydroxy-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]sulfanyl)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 18 H 29 N 1 O 2 S 1</Formula>
-<Weight type="chemical">323.50</Weight>
-<Weight type="physical">323.191900</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 15 H 24 N 0 O 1 S 0</Formula>
-<Weight type="chemical">220.36</Weight>
-<Weight type="physical">220.182715</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sakagami, Y.</Author>
-<Author>Yoshida, M.</Author>
-<Author>Isogai, A.</Author>
-<Author>Suzuki, A.</Author>
-</Authors>
-<Citation>Science 212, 1525-1527, 1981</Citation>
-<Title>Peptidal sex hormones inducing conjugation tube formation in compatible mating-type cells of Tremella mesenterica.</Title>
-<Xref>DOI:10.1126/science.212.4502.1525</Xref>
-<Xref>PMID:17790543</Xref>
-<Note>possible identification of 12-hydroxyfarnesyl</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ishibashi, Y.</Author>
-<Author>Sakagami, Y.</Author>
-<Author>Isogai, A.</Author>
-<Author>Suzuki, A.</Author>
-</Authors>
-<Citation>Biochemistry 23, 1399-1404, 1984</Citation>
-<Title>Structures of tremerogens A-9291-I and A-9291-VIII: peptidal sex hormones of Tremella brasiliensis.</Title>
-<Xref>DOI:10.1021/bi00302a010</Xref>
-<Note>mass spectrometric and (1)H-NMR characterization</Note>
-</ReferenceBlock>
-<Comment>Formation of S-12-hydroxyfarnesylcysteine may be coupled with subsequent cleavage of a carboxy-terminal tripeptide for the CAAX motif and methyl esterification of the farnesylated cysteine. See L-cysteine methyl ester (RESID:AA0105).</Comment>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Condition>incidental to RESID:AA0105</Condition>
-<Xref>GO:0018227</Xref>
-<Xref>GO:0042050</Xref>
-<Xref>PSI-MOD:00112</Xref>
-<Xref>PSI-MOD:01133</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lipoprotein</Keyword>
-<Keyword>prenylation</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__s-12-hydroxyfarnesyl cysteine__c">LIPID S-12-hydroxyfarnesyl cysteine</Feature>
-</Features>
-<Image src="/images/AA0103.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0103.PDB" />
-</Entry>
-<Entry id="AA0104">
-<Header>
-<Code>AA0104</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-geranylgeranyl-L-cysteine</Name>
-<AlternateName>2-amino-3-(3,7,11,15-tetramethyl-2,6,10,14-hexadecatetraenylthio)propanoic acid</AlternateName>
-<SystematicName>(2R)-2-amino-3-([(2E,6E,10Z)-12-hydroxy-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]sulfanyl)propanoic acid</SystematicName>
-<Xref>CAS:131404-69-8</Xref>
-<Xref>ChEBI:86021</Xref>
-<Xref>PDBHET:GER</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 23 H 37 N 1 O 1 S 1</Formula>
-<Weight type="chemical">375.62</Weight>
-<Weight type="physical">375.259586</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 20 H 32 N 0 O 0 S 0</Formula>
-<Weight type="chemical">272.48</Weight>
-<Weight type="physical">272.250401</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Morishita, R.</Author>
-<Author>Fukada, Y.</Author>
-<Author>Kokame, K.</Author>
-<Author>Yoshizawa, T.</Author>
-<Author>Masuda, K.</Author>
-<Author>Niwa, M.</Author>
-<Author>Kato, K.</Author>
-<Author>Asano, T.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 210, 1061-1069, 1992</Citation>
-<Title>Identification and isolation of common and tissue-specific geranylgeranylated gamma subunits of guanine-nucleotide-binding regulatory proteins in various tissues.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1992.tb17512.x</Xref>
-<Xref>PMID:1483450</Xref>
-<Note>mass spectrometric and chemical characterization</Note>
-</ReferenceBlock>
-<Comment>For the type I geranylgeranyltransferase the residue may be found at the first position in the sequence motif CXX[LF]* where the second and third positions are usually aliphatic.</Comment>
-<Comment>For the type II geranylgeranyltransferase the residue may be found at the first and final positions in the sequence motif CXC* or at the final two positions in the sequence motif CC*. These motifs are necessary but not sufficient for modification.</Comment>
-<Comment>Formation of S-geranylgeranylcysteine may be coupled with subsequent cleavage of a carboxy-terminal tripeptide for the CAAX motif and methyl esterification of the geranylgeranylated cysteine. Methyl esterification without cleavage occurs for the CXC motif.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>protein geranylgeranyltransferase type I</EnzymeName>
-<EnzymeName>geranylgeranyl-diphosphate:protein-cysteine geranyltransferase (EC 2.5.1.59)</EnzymeName>
-<EnzymeName>protein geranylgeranyltransferase type II</EnzymeName>
-<EnzymeName>geranylgeranyl-diphosphate:protein-cysteine geranyltransferase (EC 2.5.1.60)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Condition>incidental to RESID:AA0105</Condition>
-<Xref>GO:0018228</Xref>
-<Xref>PSI-MOD:00113</Xref>
-<Xref>PSI-MOD:01119</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lipoprotein</Keyword>
-<Keyword>prenylation</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__s-geranylgeranyl cysteine__c">LIPID S-geranylgeranyl cysteine</Feature>
-</Features>
-<Image src="/images/AA0104.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0104.PDB" />
-</Entry>
-<Entry id="AA0105">
-<Header>
-<Code>AA0105</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-cysteine methyl ester</Name>
-<AlternateName>2-amino-3-mercaptopropanoic methyl ester</AlternateName>
-<AlternateName>2-amino-3-sulfanylpropanoic methyl ester</AlternateName>
-<AlternateName>mecysteine</AlternateName>
-<AlternateName>methyl L-cysteinate</AlternateName>
-<SystematicName>methyl (2R)-2-amino-3-sulfanylpropanoate</SystematicName>
-<Xref>CAS:2485-63-3</Xref>
-<Xref>ChEBI:61989</Xref>
-<Xref>PDBHET:CMT</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 8 N 1 O 2 S 1</Formula>
-<Weight type="chemical">134.17</Weight>
-<Weight type="physical">134.027574</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 1 H 2 N 0 O 0 S 0</Formula>
-<Weight type="chemical">14.03</Weight>
-<Weight type="physical">14.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ota, I.M.</Author>
-<Author>Clarke, S.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 264, 12879-12884, 1989</Citation>
-<Title>Enzymatic methylation of 23-29-kDa bovine retinal rod outer segment membrane proteins. Evidence for methyl ester formation at carboxyl-terminal cysteinyl residues.</Title>
-<Xref>PMID:2753892</Xref>
-<Note>chemical and radiolabeling evidence for carboxyl methylation of a C-terminal cysteine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Tuinman, A.A.</Author>
-<Author>Thomas, D.A.</Author>
-<Author>Cook, K.D.</Author>
-<Author>Xue, C.B.</Author>
-<Author>Naider, F.</Author>
-<Author>Becker, J.M.</Author>
-</Authors>
-<Citation>Anal. Biochem. 193, 173-177, 1991</Citation>
-<Title>Mass spectrometric signature of S-prenylated cysteine peptides.</Title>
-<Xref>DOI:10.1016/0003-2697(91)90004-D</Xref>
-<Xref>PMID:1872463</Xref>
-<Note>mass spectrometric identification</Note>
-</ReferenceBlock>
-<Comment>The term "carboxyl methylation" applies to this modification. The terms "carboxy methylation" and "carboxymethylation" are sometimes used incorrectly for this modification. Since those terms mean "replacement by a methylcarboxylic acid", they actually refer to a different, artifactual modification.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>protein-S-isoprenylcysteine O-methyltransferase (EC 2.1.1.100)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Condition>secondary to RESID:AA0102</Condition>
-<Condition>secondary to RESID:AA0103</Condition>
-<Condition>secondary to RESID:AA0104</Condition>
-<Xref>GO:0018229</Xref>
-<Xref>PSI-MOD:00114</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>methylated carboxyl end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__cysteine methyl ester__c">MOD_RES Cysteine methyl ester</Feature>
-</Features>
-<Image src="/images/AA0105.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0105.PDB" />
-</Entry>
-<Entry id="AA0106">
-<Header>
-<Code>AA0106</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-palmitoyl-L-cysteine</Name>
-<AlternateName>2-amino-3-(hexadecanoylthio)propanoic acid</AlternateName>
-<AlternateName>cysteine hexadecanoate thioester</AlternateName>
-<AlternateName>cysteine palmitate thioester</AlternateName>
-<SystematicName>(2R)-2-amino-3-(hexadecanoylsulfanyl)propanoic acid</SystematicName>
-<Xref>CAS:114507-35-6</Xref>
-<Xref>ChEBI:74151</Xref>
-<Xref>PDBHET:PLM</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 19 H 35 N 1 O 2 S 1</Formula>
-<Weight type="chemical">341.55</Weight>
-<Weight type="physical">341.238850</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 16 H 30 N 0 O 1 S 0</Formula>
-<Weight type="chemical">238.41</Weight>
-<Weight type="physical">238.229666</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bach, R.</Author>
-<Author>Konigsberg, W.H.</Author>
-<Author>Nemerson, Y.</Author>
-</Authors>
-<Citation>Biochemistry 27, 4227-4231, 1988</Citation>
-<Title>Human tissue factor contains thioester-linked palmitate and stearate on the cytoplasmic half-cystine.</Title>
-<Xref>DOI:10.1021/bi00412a004</Xref>
-<Xref>PMID:3166978</Xref>
-<Note>chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Stults, J.T.</Author>
-<Author>Griffin, P.R.</Author>
-<Author>Lesikar, D.D.</Author>
-<Author>Naidu, A.</Author>
-<Author>Moffat, B.</Author>
-<Author>Benson, B.J.</Author>
-</Authors>
-<Citation>Am. J. Physiol. 261, L118-L125, 1991</Citation>
-<Title>Lung surfactant protein SP-C from human, bovine, and canine sources contains palmityl cysteine thioester linkages.</Title>
-<Xref>PMID:1872406</Xref>
-<Note>mass spectrometric identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Johansson, J.</Author>
-<Author>Szyperski, T.</Author>
-<Author>Curstedt, T.</Author>
-<Author>Wuthrich, K.</Author>
-</Authors>
-<Citation>Biochemistry 33, 6015-6023, 1994</Citation>
-<Title>The NMR structure of the pulmonary surfactant-associated polypeptide sp-C in an apolar solvent contains a valyl-rich alpha-helix.</Title>
-<Xref>DOI:10.1021/bi00185a042</Xref>
-<Xref>PMID:8180229</Xref>
-<Note>(1)H-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Steinert, P.M.</Author>
-<Author>Kim, S.Y.</Author>
-<Author>Chung, S.I.</Author>
-<Author>Marekov, L.N.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 271, 26242-26250, 1996</Citation>
-<Title>The transglutaminase 1 enzyme is variably acylated by myristate and palmitate during differentiation in epidermal keratinocytes.</Title>
-<Xref>DOI:10.1074/jbc.271.42.26242</Xref>
-<Xref>PMID:8824274</Xref>
-<Note>mass spectrometric identification; differential S-palmitoylation and S-myristoylation (see RESID:AA0307)</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ducker, C.E.</Author>
-<Author>Stettler, E.M.</Author>
-<Author>French, K.J.</Author>
-<Author>Upson, J.J.</Author>
-<Author>Smith, C.D.</Author>
-</Authors>
-<Citation>Oncogene 23, 9230-9237, 2004</Citation>
-<Title>Huntingtin interacting protein 14 is an oncogenic human protein: palmitoyl acyltransferase.</Title>
-<Xref>DOI:10.1038/sj.onc.1208171</Xref>
-<Xref>PMID:15489887</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Huang, K.</Author>
-<Author>Yanai, A.</Author>
-<Author>Kang, R.</Author>
-<Author>Arstikaitis, P.</Author>
-<Author>Singaraja, R.R.</Author>
-<Author>Metzler, M.</Author>
-<Author>Mullard, A.</Author>
-<Author>Haigh, B.</Author>
-<Author>Gauthier-Campbell, C.</Author>
-<Author>Gutekunst, C.A.</Author>
-<Author>Hayden, M.R.</Author>
-<Author>El-Husseini, A.</Author>
-</Authors>
-<Citation>Neuron 44, 977-986, 2004</Citation>
-<Title>Huntingtin-interacting protein HIP14 is a palmitoyl transferase involved in palmitoylation and trafficking of multiple neuronal proteins.</Title>
-<Xref>DOI:10.1016/j.neuron.2004.11.027</Xref>
-<Xref>PMID:15603740</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wilson, J.P.</Author>
-<Author>Raghavan, A.S.</Author>
-<Author>Yang, Y.Y.</Author>
-<Author>Charron, G.</Author>
-<Author>Hang, H.C.</Author>
-</Authors>
-<Citation>Mol. Cell. Proteomics 10, M110.001198, 2011</Citation>
-<Title>Proteomic analysis of fatty-acylated proteins in mammalian cells with chemical reporters reveals S-acylation of histone H3 variants.</Title>
-<Xref>DOI:10.1074/mcp.M110.001198</Xref>
-<Xref>PMID:21076176</Xref>
-<Note>biotin-tagged reagent; observed S-palmitoylation of several histone 3 varieties, in particular 3.2, in human lymphoma T cell (Jurkat) cultures</Note>
-</ReferenceBlock>
-<Comment>Although the predominant palmitoyl transferase in mammalian systems appears to utilize a mixture of saturated and unsaturated fatty acids, some systems may be more specific in their incorporation of other fatty acids.  See RESID:AA0307 and RESID:AA0308.</Comment>
-<Comment>This modification should not be confused with N-palmitoyl-cysteine (see RESID:AA0060).</Comment>
-<GeneratingEnzyme>
-<EnzymeName>protein S-acyltransferase</EnzymeName>
-<EnzymeName>palmitoyl-CoA:[protein]-L-cysteine S-palmitoyltransferase (EC 2.3.1.225)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>GO:0018230</Xref>
-<Xref>PSI-MOD:00115</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lipoprotein</Keyword>
-<Keyword>palmitoylation</Keyword>
-<Keyword>thioester bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="act_site__s-palmitoyl cysteine intermediate__c">ACT_SITE S-palmitoyl cysteine intermediate</Feature>
-<Feature type="UniProt" key="lipid__s-palmitoyl cysteine__c">LIPID S-palmitoyl cysteine</Feature>
-</Features>
-<Image src="/images/AA0106.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0106.PDB" />
-</Entry>
-<Entry id="AA0107">
-<Header>
-<Code>AA0107</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-Mar-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-diacylglycerol-L-cysteine</Name>
-<AlternateName>2-amino-3-[(S)-2-((Z)-9-octadecenoyloxy)-3-(hexadecanoyloxy)propyl]thiopropanoic acid</AlternateName>
-<AlternateName>S-(1-2'-oleoyl-3'-palmitoyl-glycerol)cysteine</AlternateName>
-<SystematicName>(2R)-2-amino-3-[(2S)-2-((9Z)-9-octadecenoyloxy)-3-(hexadecanoyloxy)propyl]sulfanylpropanoic acid</SystematicName>
-<Xref>PDBHET:DGA</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 40 H 73 N 1 O 5 S 1</Formula>
-<Weight type="chemical">680.09</Weight>
-<Weight type="physical">679.520945</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 37 H 68 N 0 O 4 S 0</Formula>
-<Weight type="chemical">576.95</Weight>
-<Weight type="physical">576.511761</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hantke, K.</Author>
-<Author>Braun, V.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 34, 284-296, 1973</Citation>
-<Title>Covalent binding of lipid to protein.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1973.tb02757.x</Xref>
-<Xref>PMID:4575979</Xref>
-<Note>chromatographic and mass spectrometric identification; chemical synthesis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Weyer, K.A.</Author>
-<Author>Schäfer, D.</Author>
-<Author>Lottspeich, F.</Author>
-<Author>Michel, H.</Author>
-</Authors>
-<Citation>Biochemistry 26, 2909-2914, 1987</Citation>
-<Title>The cytochrome subunit of the photosynthetic reaction center from Rhodopseudomonas viridis is a lipoprotein.</Title>
-<Xref>DOI:10.1021/bi00384a036</Xref>
-<Note>chromatographic and mass spectrometric identification; this amino-terminal cysteine has a free alpha-amino group</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bouchon, B.</Author>
-<Author>Klein, M.</Author>
-<Author>Bischoff, R.</Author>
-<Author>Van Dorsselaer, A.</Author>
-<Author>Roitsch, C.</Author>
-</Authors>
-<Citation>Anal. Biochem. 246, 52-61, 1997</Citation>
-<Title>Analysis of the lipidated recombinant outer surface protein A from Borrelia burgdorferi by mass spectrometry.</Title>
-<Xref>DOI:10.1006/abio.1996.9982</Xref>
-<Xref>PMID:9056182</Xref>
-<Note>mass spectrometric characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Le Hénaff, M.</Author>
-<Author>Fontenelle, C.</Author>
-</Authors>
-<Citation>Arch. Microbiol. 173, 339-345, 2000</Citation>
-<Title>Chemical analysis of processing of spiralin, the major lipoprotein of Spiroplasma melliferum.</Title>
-<Xref>DOI:10.1007/s002030000145</Xref>
-<Xref>PMID:10896212</Xref>
-<Note>chemical characterization of N-palmitoyl cysteine and S-diacylated glyceryl cysteine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kulathila, R.</Author>
-<Author>Kulathila, R.</Author>
-<Author>Indic, M.</Author>
-<Author>van den Berg, B.</Author>
-</Authors>
-<Citation>PLoS One 6, e15610, 2011</Citation>
-<Title>Crystal structure of Escherichia coli CusC, the outer membrane component of a heavy metal efflux pump.</Title>
-<Xref>DOI:10.1371/journal.pone.0015610</Xref>
-<Xref>PMID:21249122</Xref>
-<Note>X-ray diffraction, 2.30 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>van den Berg, B.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, November 2010</Citation>
-<Description>Outer membrane protein cusC.</Description>
-<Xref>PDB:3PIK</Xref>
-<Note>X-ray diffraction, 2.30 angstroms</Note>
-</ReferenceBlock>
-<Comment>The oleate and palmitate actually represent mixtures of saturated (generally at 3') and unsaturated (generally at 2') fatty acids.</Comment>
-<Comment>The signal peptide that is cleaved immediately before the modified cysteine typically ends in the motif [ILMV]X[AGS]C. Cleavage and formation of this modification may occur without N-palmitoylation, see RESID:AA0060.</Comment>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Condition>incidental to RESID:AA0060</Condition>
-<Xref>GO:0018231</Xref>
-<Xref>GO:0042050</Xref>
-<Xref>PSI-MOD:00116</Xref>
-<Xref>PSI-MOD:00898</Xref>
-<Xref>PSI-MOD:00899</Xref>
-<Xref>PSI-MOD:01144</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lipoprotein</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__s-diacylglycerol cysteine__c">LIPID S-diacylglycerol cysteine</Feature>
-</Features>
-<Image src="/images/AA0107.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0107.PDB" />
-</Entry>
-<Entry id="AA0108">
-<Header>
-<Code>AA0108</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Sep-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-(L-isoglutamyl)-L-cysteine</Name>
-<AlternateName>(S,R)-2-amino-4-[S-(2-amino-2-carboxyethyl)thiocarboxy]butanoic acid</AlternateName>
-<AlternateName>2-amino-5-(2-amino-2-carboxyethyl)thio-5-oxopentanoic acid</AlternateName>
-<AlternateName>gamma-(S-cysteinyl)glutamic acid</AlternateName>
-<SystematicName>(2S)-2-amino-5-[(2R)-2-amino-2-carboxyethyl]sulfanyl-5-oxopentanoic acid</SystematicName>
-<Xref>CAS:105580-05-0</Xref>
-<Xref>ChEBI:22021</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 8 H 10 N 2 O 3 S 1</Formula>
-<Weight type="chemical">214.24</Weight>
-<Weight type="physical">214.041213</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0007">
-<Formula>C 0 H -3 N -1 O 0 S 0</Formula>
-<Weight type="chemical">-17.03</Weight>
-<Weight type="physical">-17.026549</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Thomas, M.L.</Author>
-<Author>Tack, B.F.</Author>
-</Authors>
-<Citation>Biochemistry 22, 942-947, 1983</Citation>
-<Title>Identification and alignment of a thiol ester site in the third component of guinea pig complement.</Title>
-<Xref>DOI:10.1021/bi00273a036</Xref>
-<Xref>PMID:6838833</Xref>
-<Note>chemical characterization</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>C, Q</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>GO:0018232</Xref>
-<Xref>PSI-MOD:00117</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>thioester bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__isoglutamyl cysteine thioester (cys-gln)__c__q">CROSSLNK Isoglutamyl cysteine thioester (Cys-Gln)</Feature>
-</Features>
-<Image src="/images/AA0108.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0108.PDB" />
-</Entry>
-<Entry id="AA0109">
-<Header>
-<Code>AA0109</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-Mar-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>2'-(L-cystein-S-yl)-L-histidine</Name>
-<AlternateName>(2S)-2-amino-3-[2-([(2R)-2-amino-2-carboxyethyl]sulfanyl)-1H-imidazol-4-yl]propanoic acid</AlternateName>
-<AlternateName>S-(2'-histidyl)cysteine</AlternateName>
-<SystematicName>(2R)-2-amino-3-[(4-[(2S)-2-amino-2-carboxyethyl]-1H-imidazol-2-yl)sulfanyl]propanoic acid</SystematicName>
-<Xref>CAS:77504-36-0</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 10 N 4 O 2 S 1</Formula>
-<Weight type="chemical">238.26</Weight>
-<Weight type="physical">238.052447</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0009">
-<Formula>C 0 H -2 N 0 O 0 S 0</Formula>
-<Weight type="chemical">-2.02</Weight>
-<Weight type="physical">-2.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lerch, K.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 257, 6414-6419, 1982</Citation>
-<Title>Primary structure of tyrosinase from Neurospora crassa. II. Complete amino acid sequence and chemical structure of a tripeptide containing an unusual thioether.</Title>
-<Xref>PMID:6210696</Xref>
-<Note>chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Virador, V.M.</Author>
-<Author>Reyes Grajeda, J.P.</Author>
-<Author>Blanco-Labra, A.</Author>
-<Author>Mendiola-Olaya, E.</Author>
-<Author>Smith, G.M.</Author>
-<Author>Moreno, A.</Author>
-<Author>Whitaker, J.R.</Author>
-</Authors>
-<Citation>J. Agric. Food Chem. 58, 1189-1201, 2010</Citation>
-<Title>Cloning, sequencing, purification, and crystal structure of Grenache (Vitis vinifera) polyphenol oxidase.</Title>
-<Xref>DOI:10.1021/jf902939q</Xref>
-<Xref>PMID:20039636</Xref>
-<Note>X-ray diffraction, 2.20 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Reyes Grajeda, J.P.</Author>
-<Author>Virador, V.M.</Author>
-<Author>Blanco-Labra, A.</Author>
-<Author>Mendiola-Olaya, E.</Author>
-<Author>Smith, G.M.</Author>
-<Author>Moreno, A.</Author>
-<Author>Whitaker, J.R.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, March 2007</Citation>
-<Description>Crystal structure of Grenache (Vitis vinifera) polyphenol oxidase.</Description>
-<Xref>PDB:2P3X</Xref>
-<Note>X-ray diffraction, 2.20 angstroms</Note>
-</ReferenceBlock>
-<Comment>Cysteinylhistidine probably does not have a functional role in the enzymatic activity of Neurospora crassa tyrosinase.</Comment>
-<SequenceCode>
-<SequenceSpec>C, H</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>GO:0018233</Xref>
-<Xref>PSI-MOD:00118</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__2&apos;-(s-cysteinyl)-histidine (cys-his)__c__h">CROSSLNK 2'-(S-cysteinyl)-histidine (Cys-His)</Feature>
-</Features>
-<Image src="/images/AA0109.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0109.PDB" />
-</Entry>
-<Entry id="AA0110">
-<Header>
-<Code>AA0110</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>24-Oct-2008</StrucRevDate>
-<TextChngDate>13-Sep-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-lanthionine</Name>
-<AlternateName>(R)-S-(2-amino-2-carboxyethyl)-L-cysteine</AlternateName>
-<AlternateName>(R,R)-2,6-diamino-4-thiaheptanedioic acid</AlternateName>
-<AlternateName>(R,R)-3,3'-thiobis-(2-aminopropanoic acid)</AlternateName>
-<AlternateName>(R,R)-bis(2-amino-2-carboxyethyl)sulfide</AlternateName>
-<AlternateName>2-amino-3-(2-amino-2-carboxyethyl)sulfanylpropanoic acid</AlternateName>
-<AlternateName>3,3'-thiobis-L-alanine</AlternateName>
-<SystematicName>(2R,2'R)-3,3'-sulfanediylbis(2-aminopropanoic acid)</SystematicName>
-<Xref>CAS:922-55-4</Xref>
-<Xref>ChEBI:21347</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 8 N 2 O 2 S 1</Formula>
-<Weight type="chemical">172.20</Weight>
-<Weight type="physical">172.030649</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005" label="CYS2">
-<Formula>C 0 H -2 N 0 O 0 S -1</Formula>
-<Weight type="chemical">-34.08</Weight>
-<Weight type="physical">-33.987721</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0005 AA0016" label="CSX">
-<Formula>C 0 H -2 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sloane, N.H.</Author>
-<Author>Unich, K.G.</Author>
-</Authors>
-<Citation>Biochemistry 5, 2658-2665, 1966</Citation>
-<Title>Studies on amino acids in embryonic tissue. I. L-Lanthionine, a naturally occurring amino acid in the chick embryo.</Title>
-<Xref>DOI:10.1021/bi00872a026</Xref>
-<Xref>PMID:6007887</Xref>
-<Note>L-lanthionine and meso-lanthionine were isolated from heat and acid treated samples, and the meso form was assumed to be unnatural</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Claesen, J.</Author>
-<Author>Bibb, M.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 107, 16297-16302, 2010</Citation>
-<Title>Genome mining and genetic analysis of cypemycin biosynthesis reveal an unusual class of posttranslationally modified peptides.</Title>
-<Xref>DOI:10.1073/pnas.1008608107</Xref>
-<Xref>PMID:20805503</Xref>
-<Note>biosynthesis as an intermediate from two cysteines</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Tang, W.</Author>
-<Author>van der Donk, W.A.</Author>
-</Authors>
-<Citation>Nature Chem. Biol. 9, 157-159, 2013</Citation>
-<Title>The sequence of the enterococcal cytolysin imparts unusual lanthionine stereochemistry.</Title>
-<Xref>DOI:10.1038/nchembio.1162</Xref>
-<Xref>PMID:23314913</Xref>
-<Note>chiral gas chromatographic and mass spectrometric identification</Note>
-</ReferenceBlock>
-<Comment>This diastereomeric form, which retains the conformation of the R chiral center of L-cysteine, does occur naturally but is not common. See RESID:AA0111.</Comment>
-<SequenceCode link="CYS2">
-<SequenceSpec>C, C</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:01837</Xref>
-</SequenceCode>
-<SequenceCode link="CSX">
-<SequenceSpec>C, S</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>GO:0018081</Xref>
-<Xref>GO:0018154</Xref>
-<Xref>PSI-MOD:00119</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>lanthionine</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0110.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0110.PDB" />
-</Entry>
-<Entry id="AA0111">
-<Header>
-<Code>AA0111</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>13-Sep-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>meso-lanthionine</Name>
-<AlternateName>(2R,2'S)-3,3'-thiobis-(2-aminopropanoic acid)</AlternateName>
-<AlternateName>(2R,6S)-2,6-diamino-4-thiaheptanedioic acid</AlternateName>
-<AlternateName>(2R,6S)-meso-lanthionine</AlternateName>
-<AlternateName>(2S)-2-amino-3-[[(2R)-2-amino-2-carboxyethyl]sulfanyl]propanoic acid</AlternateName>
-<AlternateName>(2S,6R)-meso-lanthionine [misnomer]</AlternateName>
-<AlternateName>(R)-S-(2-amino-2-carboxyethyl)-D-cysteine</AlternateName>
-<AlternateName>(R,S)-bis(2-amino-2-carboxyethyl)sulfide</AlternateName>
-<AlternateName>3,3'-thiobis-meso-alanine</AlternateName>
-<AlternateName>cysteine-3-D-alanine thioether</AlternateName>
-<SystematicName>(2R,2'S)-3,3'-sulfanediylbis(2-aminopropanoic acid)</SystematicName>
-<Xref>CAS:922-56-5</Xref>
-<Xref>ChEBI:25013</Xref>
-<Xref>PDBHET:DAL</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 8 N 2 O 2 S 1</Formula>
-<Weight type="chemical">172.20</Weight>
-<Weight type="physical">172.030649</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0016">
-<Formula>C 0 H -2 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Allgaier, H.</Author>
-<Author>Jung, G.</Author>
-<Author>Werner, R.G.</Author>
-<Author>Schneider, U.</Author>
-<Author>Zaehner, H.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 160, 9-22, 1986</Citation>
-<Title>Epidermin: sequencing of a heterodet tetracyclic 21-peptide amide antibiotic.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1986.tb09933.x</Xref>
-<Xref>PMID:3769923</Xref>
-<Note>(1)H-NMR and (13)C-NMR identification; chemical synthesis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Martin, N.I.</Author>
-<Author>Sprules, T.</Author>
-<Author>Carpenter, M.R.</Author>
-<Author>Cotter, P.D.</Author>
-<Author>Hill, C.</Author>
-<Author>Ross, R.P.</Author>
-<Author>Vederas, J.C.</Author>
-</Authors>
-<Citation>Biochemistry 43, 3049-3056, 2004</Citation>
-<Title>Structural characterization of lacticin 3147, a two-peptide lantibiotic with synergistic activity.</Title>
-<Xref>DOI:10.1021/bi0362065</Xref>
-<Xref>PMID:15023056</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>He, Z.</Author>
-<Author>Kisla, D.</Author>
-<Author>Zhang, L.</Author>
-<Author>Yuan, C.</Author>
-<Author>Green-Church, K.B.</Author>
-<Author>Yousef, A.E.</Author>
-</Authors>
-<Citation>Appl. Environ. Microbiol. 73, 168-178, 2007</Citation>
-<Title>Isolation and identification of a Paenibacillus polymyxa strain that coproduces a novel lantibiotic and polymyxin.</Title>
-<Xref>DOI:10.1128/AEM.02023-06</Xref>
-<Xref>PMID:17071789</Xref>
-<Note>desulfuration and reduction with nickel dichloride and isotope labeled sodium borohydride</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Li, B.</Author>
-<Author>Sher, D.</Author>
-<Author>Kelly, L.</Author>
-<Author>Shi, Y.</Author>
-<Author>Huang, K.</Author>
-<Author>Knerr, P.J.</Author>
-<Author>Joewono, I.</Author>
-<Author>Rusch, D.</Author>
-<Author>Chisholm, S.W.</Author>
-<Author>van der Donk, W.A.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 107, 10430-10435, 2010</Citation>
-<Title>Catalytic promiscuity in the biosynthesis of cyclic peptide secondary metabolites in planktonic marine cyanobacteria.</Title>
-<Xref>DOI:10.1073/pnas.0913677107</Xref>
-<Xref>PMID:20479271</Xref>
-</ReferenceBlock>
-<Comment>This diastereomeric form, despite the appearance of the same stereochemical designator, inverts the conformation of the S chiral center of L-serine to a D-alanine skeleton with S chiralty because of the altered prority of the beta-carbon. The stereosymmetry of the meso-form is broken within a peptide chain.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptidyl-phosphoserine/phosphothreonine dehydratase (EC 4.2.1.-)</EnzymeName>
-<EnzymeName>peptidyl-cysteine dehydroalanine/dehydrobutyrine ligase (EC 6.2.-.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C, S</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>GO:0018081</Xref>
-<Xref>GO:0018155</Xref>
-<Xref>PSI-MOD:00120</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lanthionine</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__lanthionine (cys-ser)__c__s">CROSSLNK Lanthionine (Cys-Ser)</Feature>
-<Feature type="UniProt" key="crosslnk__lanthionine (ser-cys)__s__c">CROSSLNK Lanthionine (Ser-Cys)</Feature>
-</Features>
-<Image src="/images/AA0111.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0111.PDB" />
-</Entry>
-<Entry id="AA0112">
-<Header>
-<Code>AA0112</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>13-Sep-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>(2S,3S,2'R)-3-methyllanthionine</Name>
-<AlternateName>(2S,3S,2'R)-2-amino-3-[(2-amino-2-carboxyethyl)thio]butanoic acid</AlternateName>
-<AlternateName>(2S,3S,6R)-2,6-diamino-3-methyl-4-thiaheptanedioic acid</AlternateName>
-<AlternateName>(2S,3S,6R)-3-methyllanthionine</AlternateName>
-<AlternateName>(2S-[2R*,3R*(S*)])-2-amino-3-[(2-amino-2-carboxyethyl)thio]butanoic acid</AlternateName>
-<AlternateName>3-methyl-D,L-lanthionine</AlternateName>
-<AlternateName>cysteine-3-D-butyrine thioether</AlternateName>
-<SystematicName>(2S,3S)-2-amino-3-([(2R)-2-amino-2-carboxyethyl]sulfanyl)butanoic acid</SystematicName>
-<Xref>CAS:42849-28-5</Xref>
-<Xref>ChEBI:20118</Xref>
-<Xref>PDBHET:DBB</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 10 N 2 O 2 S 1</Formula>
-<Weight type="chemical">186.23</Weight>
-<Weight type="physical">186.046299</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0017">
-<Formula>C 0 H -2 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Allgaier, H.</Author>
-<Author>Jung, G.</Author>
-<Author>Werner, R.G.</Author>
-<Author>Schneider, U.</Author>
-<Author>Zaehner, H.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 160, 9-22, 1986</Citation>
-<Title>Epidermin: sequencing of a heterodet tetracyclic 21-peptide amide antibiotic.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1986.tb09933.x</Xref>
-<Xref>PMID:3769923</Xref>
-<Note>(1)H-NMR and (13)C-NMR identification; chemical synthesis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>He, Z.</Author>
-<Author>Kisla, D.</Author>
-<Author>Zhang, L.</Author>
-<Author>Yuan, C.</Author>
-<Author>Green-Church, K.B.</Author>
-<Author>Yousef, A.E.</Author>
-</Authors>
-<Citation>Appl. Environ. Microbiol. 73, 168-178, 2007</Citation>
-<Title>Isolation and identification of a Paenibacillus polymyxa strain that coproduces a novel lantibiotic and polymyxin.</Title>
-<Xref>DOI:10.1128/AEM.02023-06</Xref>
-<Xref>PMID:17071789</Xref>
-<Note>desulfuration and reduction with nickel dichloride and isotope labeled sodium borohydride</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Li, B.</Author>
-<Author>Sher, D.</Author>
-<Author>Kelly, L.</Author>
-<Author>Shi, Y.</Author>
-<Author>Huang, K.</Author>
-<Author>Knerr, P.J.</Author>
-<Author>Joewono, I.</Author>
-<Author>Rusch, D.</Author>
-<Author>Chisholm, S.W.</Author>
-<Author>van der Donk, W.A.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 107, 10430-10435, 2010</Citation>
-<Title>Catalytic promiscuity in the biosynthesis of cyclic peptide secondary metabolites in planktonic marine cyanobacteria.</Title>
-<Xref>DOI:10.1073/pnas.0913677107</Xref>
-<Xref>PMID:20479271</Xref>
-</ReferenceBlock>
-<Comment>There are 3 chiral centers, so there are 8 possible stereoisomers. Bacterial peptidyl-cysteine dehydroalanine/dehydrobutyrine ligase and peptide conformation preferentially produce the (2S,3S,2'R) diastereomer. The cysteine maintains its L configuration (R chirality), while the threonine 2-aminobutanoate skeleton has a D configuration (S chirality). For the (2R,3R,2'R) diastereomer, see RESID:AA0610.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptidyl-phosphoserine/phosphothreonine dehydratase (EC 4.2.1.-)</EnzymeName>
-<EnzymeName>peptidyl-cysteine dehydroalanine/dehydrobutyrine ligase (EC 6.2.-.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C, T</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>GO:0018081</Xref>
-<Xref>GO:0018156</Xref>
-<Xref>PSI-MOD:00121</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lanthionine</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__beta-methyllanthionine (cys-thr)__c__t">CROSSLNK Beta-methyllanthionine (Cys-Thr)</Feature>
-<Feature type="UniProt" key="crosslnk__beta-methyllanthionine (thr-cys)__t__c">CROSSLNK Beta-methyllanthionine (Thr-Cys)</Feature>
-</Features>
-<Image src="/images/AA0112.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0112.PDB" />
-</Entry>
-<Entry id="AA0113">
-<Header>
-<Code>AA0113</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-Mar-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>3'-(L-cystein-S-yl)-L-tyrosine</Name>
-<AlternateName>2-amino-3-[3-(2-amino-2-carboxyethylthio)-4-hydroxyphenyl]propanoic acid</AlternateName>
-<AlternateName>3'-(cystein-S-yl)tyrosine</AlternateName>
-<AlternateName>S-(tyros-3'-yl)cysteine</AlternateName>
-<SystematicName>(2S)-2-amino-3-(3-[(2R)2-amino-2-carboxyethylsulfanyl]-4-hydroxyphenyl)propanoic acid</SystematicName>
-<Xref>COMe:BIM000265</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 12 H 12 N 2 O 3 S 1</Formula>
-<Weight type="chemical">264.30</Weight>
-<Weight type="physical">264.056863</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0019">
-<Formula>C 0 H -2 N 0 O 0 S 0</Formula>
-<Weight type="chemical">-2.02</Weight>
-<Weight type="physical">-2.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ito, N.</Author>
-<Author>Phililips, S.E.V.</Author>
-<Author>Stevens, C.</Author>
-<Author>Ogel, Z.B.</Author>
-<Author>McPherson, M.J.</Author>
-<Author>Keen, J.N.</Author>
-<Author>Yadav, K.D.S.</Author>
-<Author>Knowles, P.F.</Author>
-</Authors>
-<Citation>Nature 350, 87-90, 1991</Citation>
-<Title>Novel thioether bond revealed by a 1.7 angstrom crystal structure of galactose oxidase.</Title>
-<Xref>DOI:10.1038/350087a0</Xref>
-<Xref>PMID:2002850</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Schnell, R.</Author>
-<Author>Sandalova, T.</Author>
-<Author>Hellman, U.</Author>
-<Author>Lindqvist, Y.</Author>
-<Author>Schneider, G.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 280, 27319-27328, 2005</Citation>
-<Title>Siroheme- and [Fe4S4]-dependent NirA from Mycobacterium tuberculosis is a sulfite reductase with a covalent Cys-Tyr bond in the active site.</Title>
-<Xref>DOI:10.1074/jbc.M502560200</Xref>
-<Xref>PMID:15917234</Xref>
-<Note>X-ray diffraction, 2.8 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Schnell, R.</Author>
-<Author>Sandalova, T.</Author>
-<Author>Hellman, U.</Author>
-<Author>Lindqvist, Y.</Author>
-<Author>Schneider, G.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, April 2005</Citation>
-<Description>Structure of Mycobacterium tuberculosis NirA protein.</Description>
-<Xref>PDB:1ZJ8</Xref>
-<Note>X-ray diffraction, 2.8 angstroms</Note>
-</ReferenceBlock>
-<Comment>In galactose oxidase, cysteinyltyrosine may exist as a stable free radical; the bond between the sulfur and the phenyl ring appears to have some double bond character.</Comment>
-<Comment>This modification should not be confused with 3-(S-L-cysteinyl)-L-tyrosine (see RESID:AA0396).</Comment>
-<SequenceCode>
-<SequenceSpec>C, Y</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>GO:0018234</Xref>
-<Xref>PSI-MOD:00122</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__3&apos;-(s-cysteinyl)-tyrosine (cys-tyr)__c__y">CROSSLNK 3'-(S-cysteinyl)-tyrosine (Cys-Tyr)</Feature>
-<Feature type="UniProt" key="crosslnk__3&apos;-(s-cysteinyl)-tyrosine (tyr-cys)__y__c">CROSSLNK 3'-(S-cysteinyl)-tyrosine (Tyr-Cys)</Feature>
-</Features>
-<Image src="/images/AA0113.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0113.PDB" />
-</Entry>
-<Entry id="AA0114">
-<Header>
-<Code>AA0114</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6-carboxy-L-lysine</Name>
-<AlternateName>2-amino-6-carbamic hexanoic acid</AlternateName>
-<AlternateName>2-amino-6-carboxamido hexanoic acid</AlternateName>
-<AlternateName>2-azanyl-6-(carboxyazanyl)hexanoic acid</AlternateName>
-<AlternateName>lysine NZ-carboxylic acid</AlternateName>
-<AlternateName>N6-carbamyllysine [misnomer]</AlternateName>
-<AlternateName>N6-carboxylysine</AlternateName>
-<SystematicName>(2S)-2-amino-6-(carboxyamino)hexanoic acid</SystematicName>
-<Xref>CAS:45101-60-8</Xref>
-<Xref>ChEBI:49185</Xref>
-<Xref>PDBHET:FMT</Xref>
-<Xref>PDBHET:KCX</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 12 N 2 O 3</Formula>
-<Weight type="chemical">172.18</Weight>
-<Weight type="physical">172.084792</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 1 H 0 N 0 O 2</Formula>
-<Weight type="chemical">44.01</Weight>
-<Weight type="physical">43.989829</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Morrow, J.S.</Author>
-<Author>Keim, P.</Author>
-<Author>Gurd, F.R.N.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 249, 7484-7494, 1974</Citation>
-<Title>CO-2 adducts of certain amino acids, peptides, and sperm whale myoglobin studied by carbon 13 and proton nuclear magnetic resonance.</Title>
-<Xref>PMID:4436319</Xref>
-<Note>(1)H-NMR and (13)C-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Stringer, C.D.</Author>
-<Author>Hartman, F.C.</Author>
-</Authors>
-<Citation>Biochem. Biophys. Res. Commun. 80, 1043-1048, 1978</Citation>
-<Title>Sequences of two active-site peptides from spinach ribulosebisphosphate carboxylase/oxygenase.</Title>
-<Xref>DOI:10.1016/0006-291X(78)91351-7</Xref>
-<Xref>PMID:637859</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Jabri, E.</Author>
-<Author>Carr, M.B.</Author>
-<Author>Hausinger, R.P.</Author>
-<Author>Karplus, P.A.</Author>
-</Authors>
-<Citation>Science 268, 998-1004, 1995</Citation>
-<Title>The crystal structure of urease from Klebsiella aerogenes.</Title>
-<Xref>DOI:10.1126/science.7754395</Xref>
-<Xref>PMID:7754395</Xref>
-<Note>X-ray diffraction, 2.2 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lapko, V.N.</Author>
-<Author>Smith, D.L.</Author>
-<Author>Smith, J.B.</Author>
-</Authors>
-<Citation>Protein Sci. 10, 1130-1136, 2001</Citation>
-<Title>In vivo carbamylation and acetylation of water-soluble human lens alphaB-crystallin lysine 92.</Title>
-<Xref>DOI:10.1110/ps.40901</Xref>
-<Xref>PMID:11369851</Xref>
-<Note>mass spectrometric detection of N6-carbamoyllysine with N6-acetyl-L-lysine; the carbamoyl group (mass 43.02) attached to an amine, forming a ureido group, and produced by reaction with cyanate or isocyanate should be carefully distinguished from the carboxy group (mass 44.01) attached to an amine, forming a carbamoyl group</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Golemi, D.</Author>
-<Author>Maveyraud, L.</Author>
-<Author>Vakulenko, S.</Author>
-<Author>Samama, J.P.</Author>
-<Author>Mobashery, S.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 98, 14280-14285, 2001</Citation>
-<Title>Critical involvement of a carbamylated lysine in catalytic function of class D beta-lactamases.</Title>
-<Xref>DOI:10.1073/pnas.241442898</Xref>
-<Xref>PMID:11724923</Xref>
-</ReferenceBlock>
-<Comment>N6-carboxylysine can be produced by artifactual, catalytic or auto-catalytic processes.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>ribulose-bisphosphate carboxylase activase (EC 6.3.4.-)</EnzymeName>
-<EnzymeName>urease activase (EC 6.3.4.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>GO:0018235</Xref>
-<Xref>PSI-MOD:00123</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="mod_res__n6-carboxylysine__k">MOD_RES N6-carboxylysine</Feature>
-</Features>
-<Image src="/images/AA0114.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0114.PDB" />
-</Entry>
-<Entry id="AA0115">
-<Header>
-<Code>AA0115</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>13-Sep-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6-(1-carboxyethyl)-L-lysine</Name>
-<AlternateName>N6-(1-carboxyethyl)lysine</AlternateName>
-<AlternateName>NZ-(1-carboxyethyl)lysine</AlternateName>
-<SystematicName>(2S)-2-amino-6-([(1S)-1-carboxyethyl]amino)hexanoic acid</SystematicName>
-<Xref>CAS:68852-50-6</Xref>
-<Xref>ChEBI:53015</Xref>
-<Xref>PDBHET:MCL</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 16 N 2 O 3</Formula>
-<Weight type="chemical">200.24</Weight>
-<Weight type="physical">200.116092</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 3 H 4 N 0 O 2</Formula>
-<Weight type="chemical">72.06</Weight>
-<Weight type="physical">72.021129</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Thompson, J.</Author>
-<Author>Miller, S.P.F.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 263, 2064-2069, 1988</Citation>
-<Title>N6-(1-carboxyethyl)lysine formation by Stretococcus lactis. Purification, synthesis, and stereochemical structure.</Title>
-<Xref>PMID:3123486</Xref>
-<Note>chromatographic detection; (1)H-NMR identification; chemical synthesis confirmation of stereochemistry</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Krook, M.</Author>
-<Author>Ghosh, D.</Author>
-<Author>Stroemberg, R.</Author>
-<Author>Carlquist, M.</Author>
-<Author>Joernvall, H.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 90, 502-506, 1993</Citation>
-<Title>Carboxyethyllysine in a protein: native carbonyl reductase/NADP+-dependent prostaglandin dehydrogenase.</Title>
-<Xref>DOI:10.1073/pnas.90.2.502</Xref>
-<Xref>PMID:8421682</Xref>
-<Note>mass spectrometric detection; (1)H-NMR identification; chemical synthesis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wermuth, B.</Author>
-<Author>Bohren, K.M.</Author>
-<Author>Ernst, E.</Author>
-</Authors>
-<Citation>FEBS Lett. 335, 151-154, 1993</Citation>
-<Title>Autocatalytic modification of human carbonyl reductase by 2-oxocarboxylic acids.</Title>
-<Xref>DOI:10.1016/0014-5793(93)80719-B</Xref>
-<Xref>PMID:8253186</Xref>
-<Note>demonstration that the modification can be produced auto-catalytically</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>GO:0018238</Xref>
-<Xref>PSI-MOD:00124</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="mod_res__n6-1-carboxyethyl lysine__k">MOD_RES N6-1-carboxyethyl lysine</Feature>
-</Features>
-<Image src="/images/AA0115.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0115.PDB" />
-</Entry>
-<Entry id="AA0116">
-<Header>
-<Code>AA0116</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-hypusine</Name>
-<AlternateName>(2S,9R)-2,11-diazanyl-9-hydroxy-7-azaundecanoic acid</AlternateName>
-<AlternateName>(2S,9R)-hypusine</AlternateName>
-<AlternateName>2-azanyl-6-[(4-azanyl-2-hydroxybutyl)azanyl]hexanoic acid</AlternateName>
-<AlternateName>epsilon-(4-amino-2-hydroxybutyl)-L-lysine</AlternateName>
-<AlternateName>N(epsilon)-(4-amino-2-hydroxybutyl)-L-lysine</AlternateName>
-<AlternateName>N(zeta)-(4-amino-2-hydroxybutyl)-L-lysine</AlternateName>
-<AlternateName>N6-(4-amino-2-hydroxybutyl)-L-lysine</AlternateName>
-<SystematicName>(2S)-2-amino-6-([(2R)-4-amino-2-hydroxybutyl]amino)hexanoic acid</SystematicName>
-<Xref>CAS:34994-11-1</Xref>
-<Xref>ChEBI:64640</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 10 H 21 N 3 O 2</Formula>
-<Weight type="chemical">215.30</Weight>
-<Weight type="physical">215.163377</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 4 H 9 N 1 O 1</Formula>
-<Weight type="chemical">87.12</Weight>
-<Weight type="physical">87.068414</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Shiba, T.</Author>
-<Author>Mizote, H.</Author>
-<Author>Kaneko, T.</Author>
-<Author>Nakajima, T.</Author>
-<Author>Kakimoto, Y.</Author>
-</Authors>
-<Citation>Biochim. Biophys. Acta 244, 523-531, 1971</Citation>
-<Title>Hypusine, a new amino acid occurring in bovine brain. Isolation and structural determination.</Title>
-<Xref>DOI:10.1016/0304-4165(71)90069-9</Xref>
-<Xref>PMID:4334286</Xref>
-<Note>isolation, mass spectrometric and (1)H-NMR identification, chemical characterization, naming</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Park, M.H.</Author>
-<Author>Cooper, H.L.</Author>
-<Author>Folk, J.E.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 257, 7217-7222, 1982</Citation>
-<Title>The biosynthesis of protein-bound hypusine (N(epsilon)-(4-amino-2-hydroxybutyl)lysine). Lysine as the amino acid precursor and the intermediate role of deoxyhypusine (N(epsilon)-(4-aminobutyl)lysine).</Title>
-<Xref>PMID:6806267</Xref>
-<Note>biosynthesis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Tice, C.M.</Author>
-<Author>Ganem, B.</Author>
-</Authors>
-<Citation>J. Org. Chem. 48, 5048-5050, 1983</Citation>
-<Title>Chemistry of naturally occurring polyamines. 8. Total synthesis of (+)-hypusine.</Title>
-<Xref>DOI:10.1021/jo00173a050</Xref>
-<Note>chemical synthesis; proof of structure and stereochemistry</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Park, M.H.</Author>
-<Author>Wolff, E.C.</Author>
-<Author>Folk, J.E.</Author>
-</Authors>
-<Citation>Trends Biochem. Sci. 18, 475-479, 1993</Citation>
-<Title>Is hypusine essential for eukaryotic cell proliferation?</Title>
-<Xref>DOI:10.1016/0968-0004(93)90010-K</Xref>
-<Xref>PMID:8108861</Xref>
-<Note>review article</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wolff, E.C.</Author>
-<Author>Kang, K.R.</Author>
-<Author>Kim, Y.S.</Author>
-<Author>Park, M.H.</Author>
-</Authors>
-<Citation>Amino Acids 33, 341-350, 2007</Citation>
-<Title>Posttranslational synthesis of hypusine: evolutionary progression and specificity of the hypusine modification.</Title>
-<Xref>DOI:10.1007/s00726-007-0525-0</Xref>
-<Xref>PMID:17476569</Xref>
-<Note>evolutionary considerations</Note>
-</ReferenceBlock>
-<Comment>Hypusine appears to occur uniquely in translation initiation factor eIF-5A. For the detectable intermediate form, L-deoxyhypusine, in either deoxyhypusine synthase or in initiation factor 5A, eIF5A, see RESID:AA0564.</Comment>
-<Comment>It is highly probable that, like prokaryotic elongation factor EF-P, eIF-5A acts to relieve ribosome stalling during the translation of polyproline and prolylglycine sequences. The hypusine residue may extend into the ribosome active site and assist in catalysis of the petidyl transfer.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>deoxyhypusine synthase (EC 2.5.1.46)</EnzymeName>
-<EnzymeName>deoxyhypusine monooxygenase (EC 1.14.99.29)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>GO:0008612</Xref>
-<Xref>PSI-MOD:00125</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-<Keyword>hypusine</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__hypusine__k">MOD_RES Hypusine</Feature>
-</Features>
-<Image src="/images/AA0116.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0116.PDB" />
-</Entry>
-<Entry id="AA0117">
-<Header>
-<Code>AA0117</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6-biotinyl-L-lysine</Name>
-<AlternateName>(3aS-(3aalpha,4beta,6aalpha))-N6-(5-(hexahydro-2-oxo-1H-thieno(3,4-d)imidazol-4-yl)-1-oxopentyl)-L-lysine</AlternateName>
-<AlternateName>biocytin</AlternateName>
-<AlternateName>epsilon-N-biotinyllysine</AlternateName>
-<AlternateName>N6-biotinyllysine</AlternateName>
-<AlternateName>N6-[5-((3aS,4S,6aR)-hexahydro-2-oxo-1H-thieno[3,4-d]imidazol-4-yl)-1-oxopentyl]-L-lysine</AlternateName>
-<SystematicName>(2S)-2-amino-6-(5-[(3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl]pentanoylamino)hexanoic acid</SystematicName>
-<Xref>CAS:576-19-2</Xref>
-<Xref>CAS:58-85-5</Xref>
-<Xref>ChEBI:83144</Xref>
-<Xref>COMe:BIM000388</Xref>
-<Xref>PDBHET:BTN</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 16 H 26 N 4 O 3 S 1</Formula>
-<Weight type="chemical">354.47</Weight>
-<Weight type="physical">354.172562</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 10 H 14 N 2 O 2 S 1</Formula>
-<Weight type="chemical">226.29</Weight>
-<Weight type="physical">226.077599</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Thampy, K.G.</Author>
-<Author>Huang, W.Y.</Author>
-<Author>Wakil, S.J.</Author>
-</Authors>
-<Citation>Arch. Biochem. Biophys. 266, 270-276, 1988</Citation>
-<Title>A rapid purification method for rat liver pyruvate carboxylase and amino acid sequence analyses of NH2-terminal and biotin peptide.</Title>
-<Xref>DOI:10.1016/0003-9861(88)90258-5</Xref>
-<Xref>PMID:3178228</Xref>
-<Note>affinity chromatography and chromatographic detection</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Duval, M.</Author>
-<Author>DeRose, R.T.</Author>
-<Author>Job, C.</Author>
-<Author>Faucher, D.</Author>
-<Author>Douce, R.</Author>
-<Author>Job, D.</Author>
-</Authors>
-<Citation>Plant Mol. Biol. 26, 265-273, 1994</Citation>
-<Title>The major biotinyl protein from Pisum sativum seeds covalently binds biotin at a novel site.</Title>
-<Xref>DOI:10.1007/BF00039537</Xref>
-<Xref>PMID:7948875</Xref>
-<Note>biotin covalently bound at a site differing from the usual biotin binding homology</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Athappilly, F.K.</Author>
-<Author>Hendrickson, W.A.</Author>
-</Authors>
-<Citation>Structure 3, 1407-1419, 1995</Citation>
-<Title>Structure of the biotinyl domain of acetyl-coenzyme A carboxylase determined by MAD phasing.</Title>
-<Xref>DOI:10.1016/S0969-2126(01)00277-5</Xref>
-<Xref>PMID:8747466</Xref>
-<Note>X-ray diffraction, 1.8 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Athappilly, F.K.</Author>
-<Author>Hendrickson, W.A.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, November 1995</Citation>
-<Description>Structure of the biotinyl domain of acetyl-coenzyme A carboxylase determined by MAD phasing.</Description>
-<Xref>PDB:1BDO</Xref>
-<Note>X-ray diffraction, 1.8 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Chew, Y.C.</Author>
-<Author>Camporeale, G.</Author>
-<Author>Kothapalli, N.</Author>
-<Author>Sarath, G.</Author>
-<Author>Zempleni, J.</Author>
-</Authors>
-<Citation>J. Nutr. Biochem. 17, 225-233, 2006</Citation>
-<Title>Lysine residues in N-terminal and C-terminal regions of human histone H2A are targets for biotinylation by biotinidase.</Title>
-<Xref>DOI:10.1016/j.jnutbio.2005.05.003</Xref>
-<Xref>PMID:16109483</Xref>
-<Note>reports the natural biotinylation of histone lysines</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>biotin--protein ligase (EC 6.3.4.-)</EnzymeName>
-<EnzymeName>biotin--[methylmalonyl-CoA-carboxyltransferase] ligase (EC 6.3.4.9)</EnzymeName>
-<EnzymeName>biotin--[propionyl-CoA-carboxylase (ATP-hydrolysing)] ligase (EC 6.3.4.10)</EnzymeName>
-<EnzymeName>biotin--[methylcrotonoyl-CoA-carboxylase] ligase (EC 6.3.4.11)</EnzymeName>
-<EnzymeName>biotin--[acetyl-CoA-carboxylase] ligase (EC 6.3.4.15)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>GO:0018054</Xref>
-<Xref>PSI-MOD:00126</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>biotin</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n6-biotinyllysine__k">MOD_RES N6-biotinyllysine</Feature>
-</Features>
-<Image src="/images/AA0117.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0117.PDB" />
-</Entry>
-<Entry id="AA0118">
-<Header>
-<Code>AA0118</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6-lipoyl-L-lysine</Name>
-<AlternateName>(2S)-2-amino-6-(5-[(3R)-1,2-dithiolan-3-yl]pentanamido)hexanoic acid</AlternateName>
-<AlternateName>(2S,6'R)-2-amino-6-(6,8-dithiooctanamido)hexanoic acid</AlternateName>
-<AlternateName>2-amino-6-(5-[1,2-dithiolan-3-yl]-1-oxopentyl)aminohexanoic acid</AlternateName>
-<AlternateName>N6-6,8-dithiooctanoyllysine</AlternateName>
-<AlternateName>N6-lipoyllysine</AlternateName>
-<SystematicName>(2S)-2-amino-6-[(5-[(3R)-1,2-dithiolan-3-yl]pentanoyl)amino]hexanoic acid</SystematicName>
-<Xref>CAS:1200-22-2</Xref>
-<Xref>CAS:1676-89-7</Xref>
-<Xref>ChEBI:14919</Xref>
-<Xref>COMe:BIM000394</Xref>
-<Xref>PDBHET:LPA</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 14 H 24 N 2 O 2 S 2</Formula>
-<Weight type="chemical">316.48</Weight>
-<Weight type="physical">316.127920</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 8 H 12 N 0 O 1 S 2</Formula>
-<Weight type="chemical">188.30</Weight>
-<Weight type="physical">188.032957</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fujiwara, K.</Author>
-<Author>Okamura-Ikeda, K.</Author>
-<Author>Motokawa, Y.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 261, 8836-8841, 1986</Citation>
-<Title>Chicken liver H-protein, a component of the glycine cleavage system: amino acid sequence and identification of the N-lipoyllysine residue.</Title>
-<Xref>PMID:3522581</Xref>
-<Note>detection of radioisotope labeled N-ethylmaleimide PTH derivative</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Packman, L.C.</Author>
-<Author>Borges, A.</Author>
-<Author>Perham, R.N.</Author>
-</Authors>
-<Citation>Biochem. J. 252, 79-86, 1988</Citation>
-<Title>Amino acid sequence analysis of the lipoyl and peripheral subunit-binding domains in the lipoate acetyltransferase component of the pyruvate dehydrogenase complex from Bacillus stearothermophilus.</Title>
-<Xref>PMID:3421911</Xref>
-<Note>mass spectrometric identification of bis-pyridethylated derivative</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Cohen-Addad, C.</Author>
-<Author>Pares, S.</Author>
-<Author>Sieker, L.</Author>
-<Author>Neuburger, M.</Author>
-<Author>Douce, R.</Author>
-</Authors>
-<Citation>Nature Struct. Biol. 2, 63-68, 1995</Citation>
-<Title>The lipoamide arm in the glycine decarboxylase complex is not freely swinging.</Title>
-<Xref>DOI:10.1038/nsb0195-63</Xref>
-<Xref>PMID:7719855</Xref>
-<Note>X-ray diffraction, 2.6 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Pares, S.</Author>
-<Author>Cohen-Addad, C.</Author>
-<Author>Sieker, L.</Author>
-<Author>Neuburger, M.</Author>
-<Author>Douce, R.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, February 1994</Citation>
-<Description>H protein of the glycine cleavage system (aminomethyltransferase) (E.C.1.4.4.2).</Description>
-<Xref>PDB:1HPC</Xref>
-<Note>X-ray diffraction, 2.6 angstroms</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>lipoate--protein ligase</EnzymeName>
-<EnzymeName>[lipoyl-carrier protein]-L-lysine:lipoate ligase (AMP-forming) (EC 6.3.1.20)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>GO:0018055</Xref>
-<Xref>PSI-MOD:00127</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lipoamide</Keyword>
-<Keyword>redox-active center</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n6-lipoyllysine__k">MOD_RES N6-lipoyllysine</Feature>
-</Features>
-<Image src="/images/AA0118.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0118.PDB" />
-</Entry>
-<Entry id="AA0119">
-<Header>
-<Code>AA0119</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Jun-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6-pyridoxal phosphate-L-lysine</Name>
-<SystematicName>(2S)-2-amino-6-[([3-hydroxy-2-methyl-5-phosphonooxymethylpyridin-4-yl]methylidene)amino]hexanoic acid</SystematicName>
-<Xref>CAS:2440-59-7</Xref>
-<Xref>COMe:BIM000270</Xref>
-<Xref>PDBHET:LLP</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 14 H 20 N 3 O 6 P 1</Formula>
-<Weight type="chemical">357.30</Weight>
-<Weight type="physical">357.108972</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 8 H 8 N 1 O 5 P 1</Formula>
-<Weight type="chemical">229.13</Weight>
-<Weight type="physical">229.014009</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bohney, J.P.</Author>
-<Author>Fonda, M.L.</Author>
-<Author>Feldhoff, R.C.</Author>
-</Authors>
-<Citation>FEBS Lett. 298, 266-268, 1992</Citation>
-<Title>Identification of Lys(190) as the primary binding site for pyridoxal 5'-phosphate in human serum albumin.</Title>
-<Xref>DOI:10.1016/0014-5793(92)80073-P</Xref>
-<Xref>PMID:1544460</Xref>
-<Note>sequencing after reaction with (3)H-pyridoxal phosphate and borohydride reduction</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>GO:0018272</Xref>
-<Xref>PSI-MOD:00128</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>phosphoprotein</Keyword>
-<Keyword>pyridine ring</Keyword>
-<Keyword>pyridoxal phosphate</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n6-(pyridoxal phosphate)lysine__k">MOD_RES N6-(pyridoxal phosphate)lysine</Feature>
-</Features>
-<Image src="/images/AA0119.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0119.PDB" />
-</Entry>
-<Entry id="AA0120">
-<Header>
-<Code>AA0120</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Sep-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6-retinylidene-L-lysine</Name>
-<AlternateName>N6-retinal-L-lysine</AlternateName>
-<AlternateName>N6-retinyl-lysine</AlternateName>
-<SystematicName>(2S)-2-amino-6-[(2E,4E,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-en-1-yl)-2,4,6,8-nonatetraenylidene]aminohexanoic acid</SystematicName>
-<Xref>CAS:116-31-4</Xref>
-<Xref>CAS:130443-70-8</Xref>
-<Xref>COMe:BIM000139</Xref>
-<Xref>PDBHET:LYR</Xref>
-<Xref>PDBHET:RET</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 26 H 38 N 2 O 1</Formula>
-<Weight type="chemical">394.60</Weight>
-<Weight type="physical">394.298414</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 20 H 26 N 0 O 0</Formula>
-<Weight type="chemical">266.43</Weight>
-<Weight type="physical">266.203451</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mullen, E.</Author>
-<Author>Akhtar, M.</Author>
-</Authors>
-<Citation>Biochem. J. 211, 45-54, 1983</Citation>
-<Title>Structural studies on membrane-bound bovine rhodopsin.</Title>
-<Xref>PMID:6870827</Xref>
-<Note>chemical conversion and identification as carboxymethyllysine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Katre, N.V.</Author>
-<Author>Wolber, P.K.</Author>
-<Author>Stoeckenius, W.</Author>
-<Author>Stroud, R.M.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 78, 4068-4072, 1981</Citation>
-<Title>Attachment site(s) of retinal in bacteriorhodopsin.</Title>
-<Xref>DOI:10.1073/pnas.78.7.4068</Xref>
-<Xref>PMID:6794028</Xref>
-<Note>radioisotope labeling; chemical conversion and identification as retinyllysine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Standfuss, J.</Author>
-<Author>Xie, G.</Author>
-<Author>Edwards, P.C.</Author>
-<Author>Burghammer, M.</Author>
-<Author>Oprian, D.D.</Author>
-<Author>Schertler, G.F.X.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 372, 1179-1188, 2007</Citation>
-<Title>Crystal structure of a thermally stable rhodopsin mutant.</Title>
-<Xref>DOI:10.1016/j.jmb.2007.03.007</Xref>
-<Xref>PMID:17825322</Xref>
-<Note>X-ray diffraction, 3.40 angstroms; the initials of "G.F. Schertler" in the PubMed citation are corrected</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Standfuss, J.</Author>
-<Author>Xie, G.</Author>
-<Author>Edwards, P.C.</Author>
-<Author>Burghammer, M.</Author>
-<Author>Oprian, D.D.</Author>
-<Author>Schertler, G.F.X.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, September 2006</Citation>
-<Description>Crystal structure of a rhodopsin stabilizing mutant  expressed in mammalian cells.</Description>
-<Xref>PDB:2J4Y</Xref>
-<Note>X-ray diffraction, 2.60 angstroms</Note>
-</ReferenceBlock>
-<Comment>The all-trans form is shown. Light-induced interconversion with the 11-cis (4Z) form in rhodopsin is the basis for light sensing in animals. Light-induced interconversion with the 13-cis (2Z) form in bacteriorhodopsin is utilized for proton pumping in some archaea.</Comment>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>GO:0018273</Xref>
-<Xref>PSI-MOD:00129</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chromoprotein</Keyword>
-<Keyword>retinal</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n6-(retinylidene)lysine__k">MOD_RES N6-(retinylidene)lysine</Feature>
-</Features>
-<Image src="/images/AA0120.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0120.PDB" />
-</Entry>
-<Entry id="AA0121">
-<Header>
-<Code>AA0121</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-allysine</Name>
-<AlternateName>2-amino-5-formylvaleric acid</AlternateName>
-<AlternateName>2-amino-adipic acid semialdahyde</AlternateName>
-<AlternateName>2-aminoadipate 6-semialdehyde</AlternateName>
-<AlternateName>5-formyl-norvaline</AlternateName>
-<AlternateName>6-oxonorleucine</AlternateName>
-<AlternateName>AASA</AlternateName>
-<AlternateName>alpha-amino-adipic acid delta-semialdahyde</AlternateName>
-<SystematicName>(2S)-2-amino-6-oxohexanoic acid</SystematicName>
-<Xref>CAS:1962-83-0</Xref>
-<Xref>CAS:6665-12-9</Xref>
-<Xref>ChEBI:131803</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 9 N 1 O 2</Formula>
-<Weight type="chemical">127.14</Weight>
-<Weight type="physical">127.063329</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 0 H -3 N -1 O 1</Formula>
-<Weight type="chemical">-1.03</Weight>
-<Weight type="physical">-1.031634</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kang, A.H.</Author>
-<Author>Bornstein, P.</Author>
-<Author>Piez, K.A.</Author>
-</Authors>
-<Citation>Biochemistry 6, 788-795, 1967</Citation>
-<Title>The amino acid sequence of peptides from the cross-linking region of rat skin collagen.</Title>
-<Xref>DOI:10.1021/bi00855a019</Xref>
-<Xref>PMID:5337886</Xref>
-<Note>chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Click, E.M.</Author>
-<Author>Bornstein, P.</Author>
-</Authors>
-<Citation>Biochemistry 9, 4699-4706, 1970</Citation>
-<Title>Isolation and characterization of the cyanogen bromide peptides from the alpha 1 and alpha 2 chains of human skin collagen.</Title>
-<Xref>DOI:10.1021/bi00826a012</Xref>
-<Xref>PMID:5529814</Xref>
-<Note>chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Diedrich, D.L.</Author>
-<Author>Schnaitman, C.A.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 75, 3708-3712, 1978</Citation>
-<Title>Lysyl-derived aldehydes in outer membrane proteins of Escherichia coli.</Title>
-<Xref>DOI:10.1073/pnas.75.8.3708</Xref>
-<Xref>PMID:358196</Xref>
-<Note>mass spectrometric detection</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Umeda, H.</Author>
-<Author>Kawamorita, K.</Author>
-<Author>Suyama, K.</Author>
-</Authors>
-<Citation>Amino Acids 20, 187-199, 2001</Citation>
-<Title>High-performance liquid chromatographic quantification of allysine as bis-p-cresol derivative in elastin.</Title>
-<Xref>DOI:10.1007/s007260170059</Xref>
-<Xref>PMID:11332453</Xref>
-<Note>chromatographic detection</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Herranz, N.</Author>
-<Author>Dave, N.</Author>
-<Author>Millanes-Romero, A.</Author>
-<Author>Morey, L.</Author>
-<Author>Díaz, V.M.</Author>
-<Author>Lórenz-Fonfría, V.</Author>
-<Author>Gutierrez-Gallego, R.</Author>
-<Author>Jerónimo, C.</Author>
-<Author>Di Croce, L.</Author>
-<Author>García de Herreros, A.</Author>
-<Author>Peiró, S.</Author>
-</Authors>
-<Citation>Mol. Cell 46, 369-376, 2012</Citation>
-<Title>Lysyl oxidase-like 2 deaminates lysine 4 in histone H3.</Title>
-<Xref>DOI:10.1016/j.molcel.2012.03.002</Xref>
-<Xref>PMID:22483618</Xref>
-<Note>mass spectrometric detection; lysyl oxidase-like 2, LOXL2, is reported to convert histone H3-trimethyl-lysine-4 to allysine</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>protein-lysine 6-oxidase (EC 1.4.3.13)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Condition>incidental to RESID:AA0028</Condition>
-<Xref>GO:0018057</Xref>
-<Xref>PSI-MOD:00130</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="mod_res__allysine__k">MOD_RES Allysine</Feature>
-</Features>
-<Image src="/images/AA0121.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0121.PDB" />
-</Entry>
-<Entry id="AA0122">
-<Header>
-<Code>AA0122</Code>
-<Dates>
-<CreationDate>02-Nov-2001</CreationDate>
-<StrucRevDate>02-Nov-2001</StrucRevDate>
-<TextChngDate>30-Sep-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-2-aminoadipic acid</Name>
-<AlternateName>2-amino-1,4-butanedicarboxylic acid</AlternateName>
-<AlternateName>L-alpha-aminoadipic acid</AlternateName>
-<SystematicName>(2S)-2-aminohexanedioic acid</SystematicName>
-<Xref>CAS:1118-90-7</Xref>
-<Xref>CAS:542-32-5</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 9 N 1 O 3</Formula>
-<Weight type="chemical">143.14</Weight>
-<Weight type="physical">143.058243</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 0 H -3 N -1 O 2</Formula>
-<Weight type="chemical">14.97</Weight>
-<Weight type="physical">14.963280</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hiraoka, B.Y.</Author>
-<Author>Fukasawa, K.</Author>
-<Author>Fukasawa, K.M.</Author>
-<Author>Harada, M.</Author>
-</Authors>
-<Citation>J. Biochem. 88, 373-377, 1980</Citation>
-<Title>Identification and quantification of alpha-amino adipic acid in bovine dentine phosphoprotein.</Title>
-<Xref>PMID:7419498</Xref>
-<Note>chromatographic detection</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Diedrich, D.L.</Author>
-<Author>Schnaitman, C.A.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 75, 3708-3712, 1978</Citation>
-<Title>Lysyl-derived aldehydes in outer membrane proteins of Escherichia coli.</Title>
-<Xref>DOI:10.1073/pnas.75.8.3708</Xref>
-<Xref>PMID:358196</Xref>
-<Note>mass spectrometric characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bailey, A.J.</Author>
-<Author>Ranta, M.H.</Author>
-<Author>Nicholls, A.C.</Author>
-<Author>Partridge, S.M.</Author>
-<Author>Elsden, D.F.</Author>
-</Authors>
-<Citation>Biochem. Biophys. Res. Commun. 78, 1403-1410, 1977</Citation>
-<Title>Isolation of alpha-amino adipic acid from mature dermal collagen and elastin. Evidence for an oxidative pathway in the maturation of collagen and elastin.</Title>
-<Xref>DOI:10.1016/0006-291X(77)91448-6</Xref>
-<Xref>PMID:336041</Xref>
-</ReferenceBlock>
-<Comment>The oxidation of allysine to 2-aminoadipic acid is not well characterized.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>protein-lysine 6-oxidase (EC 1.4.3.13)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>GO:0019728</Xref>
-<Xref>PSI-MOD:00131</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0122.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0122.PDB" />
-</Entry>
-<Entry id="AA0123">
-<Header>
-<Code>AA0123</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-lysinoalanine</Name>
-<AlternateName>(2R,9S)-lysinoalanine</AlternateName>
-<AlternateName>alaninolysine</AlternateName>
-<AlternateName>LAL</AlternateName>
-<AlternateName link="LYS">lysino-D-alanine</AlternateName>
-<AlternateName>N-epsilon-(2-amino-2-carboxyethyl)-L-lysine</AlternateName>
-<AlternateName>N6-(2-amino-2-carboxyethyl)-L-lysine</AlternateName>
-<SystematicName>(2S)-2-amino-6-([(2R)-2-amino-2-carboxyethyl]amino)hexanoic acid</SystematicName>
-<Xref>CAS:18810-04-3</Xref>
-</Names>
-<FormulaBlock label="KSX">
-<Formula>C 9 H 15 N 3 O 2</Formula>
-<Weight type="chemical">197.24</Weight>
-<Weight type="physical">197.116427</Weight>
-</FormulaBlock>
-<FormulaBlock label="LYS">
-<Formula>C 9 H 17 N 3 O 3</Formula>
-<Weight type="chemical">215.25</Weight>
-<Weight type="physical">215.126991</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012 AA0016" link="KSX">
-<Formula>C 0 H -2 N 0 O -1</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0012" link="LYS">
-<Formula>C 3 H 5 N 1 O 2</Formula>
-<Weight type="chemical">87.08</Weight>
-<Weight type="physical">87.032028</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Naruse, N.</Author>
-<Author>Tenmyo, O.</Author>
-<Author>Tomita, K.</Author>
-<Author>Konishi, M.</Author>
-<Author>Miyaki, T.</Author>
-<Author>Kawaguchi, H.</Author>
-<Author>Fukase, K.</Author>
-<Author>Wakamiya, T.</Author>
-<Author>Shiba, T.</Author>
-</Authors>
-<Citation>J. Antibiot. 42, 837-845, 1989</Citation>
-<Title>Lanthiopeptin, a new peptide antibiotic. Production, isolation and properties of lanthiopeptin.</Title>
-<Xref>PMID:2544544</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yamauchi, T.</Author>
-<Author>Goto, M.</Author>
-<Author>Wu, H.Y.</Author>
-<Author>Uo, T.</Author>
-<Author>Yoshimura, T.</Author>
-<Author>Mihara, H.</Author>
-<Author>Kurihara, T.</Author>
-<Author>Miyahara, I.</Author>
-<Author>Hirotsu, K.</Author>
-<Author>Esaki, N.</Author>
-</Authors>
-<Citation>J. Biochem. 145, 421-424, 2009</Citation>
-<Title>Serine racemase with catalytically active lysinoalanyl residue.</Title>
-<Xref>DOI:10.1093/jb/mvp010</Xref>
-<Xref>PMID:19155267</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hosoda, K.</Author>
-<Author>Ohya, M.</Author>
-<Author>Kohno, T.</Author>
-<Author>Maeda, T.</Author>
-<Author>Endo, S.</Author>
-<Author>Wakamatsu, K.</Author>
-</Authors>
-<Citation>J. Biochem. 119, 226-230, 1996</Citation>
-<Title>Structure determination of an immunopotentiator peptide, cinnamycin, complexed with lysophosphatidylethanolamine by 1H-NMR1.</Title>
-<Xref>PMID:8882709</Xref>
-<Note>(1)H-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hosoda, K.</Author>
-<Author>Ohya, M.</Author>
-<Author>Kohno, T.</Author>
-<Author>Maeda, T.</Author>
-<Author>Endo, S.</Author>
-<Author>Wakamatsu, K.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, January 2006</Citation>
-<Description>Structure of cinnamycin complexed with lysophosphatidylethanolamine.</Description>
-<Xref>PDB:2DDE</Xref>
-<Note>NMR</Note>
-</ReferenceBlock>
-<Comment>The formula and records labeled "KSX" refers to a lysinoalanine residue produced as a cross-link between a peptidyl lysine and a peptidyl serine residue. For the cross-link the stereochemistry of the second chiral center has not been resolved; it appears to epimerize rapidly during acid hydrolysis. The (2R,9S) form is shown.</Comment>
-<Comment>The formula and records labeled "LYS" refers to a lysinoalanine residue produced as a peptidyl lysine residue bonded to a free serine. For the lysine modification by D-serine, the diastereomer is (2R,9S).</Comment>
-<SequenceCode link="KSX">
-<SequenceSpec>K, S</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>GO:0018274</Xref>
-<Xref>PSI-MOD:00132</Xref>
-</SequenceCode>
-<SequenceCode link="LYS">
-<SequenceSpec>K</SequenceSpec>
-<Xref>PSI-MOD:01838</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="crosslnk__lysinoalanine (ser-lys)__s__k" link="KSX">CROSSLNK Lysinoalanine (Ser-Lys)</Feature>
-<Feature type="UniProt" key="mod_res__lysino-d-alanine (lys)__k" link="LYS">MOD_RES Lysino-D-alanine (Lys)</Feature>
-</Features>
-<Image src="/images/AA0123.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0123.PDB" />
-</Entry>
-<Entry id="AA0124">
-<Header>
-<Code>AA0124</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>13-Sep-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6-(L-isoglutamyl)-L-lysine</Name>
-<AlternateName>2-azanyl-6-([4-azanyl-4-carboxybutanoyl]azanyl)hexanoic acid</AlternateName>
-<AlternateName>5-glutamyl N6-lysine</AlternateName>
-<AlternateName>N(epsilon)-(gamma-glutamyl)lysine</AlternateName>
-<SystematicName>(2S)-2-amino-6-([(4S)-4-amino-4-carboxybutanoyl]amino)hexanoic acid</SystematicName>
-<Xref>CAS:17105-15-6</Xref>
-<Xref>ChEBI:21863</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 11 H 17 N 3 O 3</Formula>
-<Weight type="chemical">239.27</Weight>
-<Weight type="physical">239.126991</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0007 AA0012" label="GLN">
-<Formula>C 0 H -3 N -1 O 0</Formula>
-<Weight type="chemical">-17.03</Weight>
-<Weight type="physical">-17.026549</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0006 AA0012" label="GLU">
-<Formula>C 0 H -2 N 0 O -1</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lorand, L.</Author>
-<Author>Downey, J.</Author>
-<Author>Gotoh, T.</Author>
-<Author>Jacobsen, A.</Author>
-<Author>Tokura, S.</Author>
-</Authors>
-<Citation>Biochem. Biophys. Res. Commun. 31, 222-230, 1968</Citation>
-<Title>The transpeptidase system which crosslinks fibrin by gamma-glutamyl-epsilon-lysine bonds.</Title>
-<Xref>DOI:10.1016/0006-291X(68)90734-1</Xref>
-<Xref>PMID:5656070</Xref>
-<Note>title typographical errors in the PubMed citation are corrected</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Matačić, S.</Author>
-<Author>Loewy, A.G.</Author>
-</Authors>
-<Citation>Biochem. Biophys. Res. Commun. 30, 356-362, 1968</Citation>
-<Title>The identification of isopeptide crosslinks in insoluble fibrin.</Title>
-<Xref>DOI:10.1016/0006-291X(68)90750-X</Xref>
-<Xref>PMID:5637041</Xref>
-<Note>chemical characterization; the encoding of an author's name in the PubMed citation is corrected to UTF8</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Simon, M.</Author>
-<Author>Green, H.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 263, 18093-18098, 1988</Citation>
-<Title>The glutamine residues reactive in transglutaminase-catalyzed cross-linking of involucrin.</Title>
-<Xref>PMID:2461365</Xref>
-<Note>radioisotope labeling and linkage analysis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Shimizu, T.</Author>
-<Author>Hozumi, K.</Author>
-<Author>Horiike, S.</Author>
-<Author>Nunomura, K.</Author>
-<Author>Ikegami, S.</Author>
-<Author>Takao, T.</Author>
-<Author>Shimonishi, Y.</Author>
-</Authors>
-<Citation>Nature 380, 32, 1996</Citation>
-<Title>A covalently crosslinked histone.</Title>
-<Xref>DOI:10.1038/380032a0</Xref>
-<Xref>PMID:8598899</Xref>
-<Note>mass spectrometric and linkage analysis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kudryashov, D.S.</Author>
-<Author>Durer, Z.A.</Author>
-<Author>Ytterberg, A.J.</Author>
-<Author>Sawaya, M.R.</Author>
-<Author>Pashkov, I.</Author>
-<Author>Prochazkova, K.</Author>
-<Author>Yeates, T.O.</Author>
-<Author>Loo, R.R.</Author>
-<Author>Loo, J.A.</Author>
-<Author>Satchell, K.J.</Author>
-<Author>Reisler, E.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 105, 18537-18542, 2008</Citation>
-<Title>Connecting actin monomers by iso-peptide bond is a toxicity mechanism of the Vibrio cholerae MARTX toxin.</Title>
-<Xref>DOI:10.1073/pnas.0808082105</Xref>
-<Xref>PMID:19015515</Xref>
-<Note>mass spectrometric identification; X-ray diffraction, 3.21 angstroms; ATP is required to produce the isopeptide bond between lysine and glutamic acid</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sawaya, M.R.</Author>
-<Author>Kudryashov, D.S.</Author>
-<Author>Pashkov, I.</Author>
-<Author>Reisler, E.</Author>
-<Author>Loo, R.R.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, March 2008</Citation>
-<Description>Actin dimer cross-linked by V. cholerae MARTX toxin and complexed with gelsolin-segment 1.</Description>
-<Xref>PDB:3CJB</Xref>
-<Note>X-ray diffraction, 3.21 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Pearce, M.J.</Author>
-<Author>Mintseris, J.</Author>
-<Author>Ferreyra, J.</Author>
-<Author>Gygi, S.P.</Author>
-<Author>Darwin, K.H.</Author>
-</Authors>
-<Citation>Science 322, 1104-1107, 2008</Citation>
-<Title>Ubiquitin-like protein involved in the proteasome pathway of Mycobacterium tuberculosis.</Title>
-<Xref>DOI:10.1126/science.1163885</Xref>
-<Xref>PMID:18832610</Xref>
-<Note>identification of prokaryotic ubiquitin-like protein, pup, cross-linkage of terminal glutamine to N6-lysine after deamidation</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Iyer, L.M.</Author>
-<Author>Burroughs, A.M.</Author>
-<Author>Aravind, L.</Author>
-</Authors>
-<Citation>Biol. Direct 3, 45, 2008</Citation>
-<Title>Unraveling the biochemistry and provenance of pupylation: a prokaryotic analog of ubiquitination.</Title>
-<Xref>DOI:10.1186/1745-6150-3-45</Xref>
-<Xref>PMID:18980670</Xref>
-<Note>the homology of pafa, which activates the C-terminal glutamate of pup, suggests but does not establish that the linkage is through the gamma-carboxyl; the pup homologs in various bacteria have either glutamine or glutamic acid as the C-terminus</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sutter, M.</Author>
-<Author>Damberger, F.F.</Author>
-<Author>Imkamp, F.</Author>
-<Author>Allain, F.H.</Author>
-<Author>Weber-Ban, E.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 132, 5610-5612, 2010</Citation>
-<Title>Prokaryotic ubiquitin-like protein (Pup) is coupled to substrates via the side chain of its C-terminal glutamate.</Title>
-<Xref>DOI:10.1021/ja910546x</Xref>
-<Xref>PMID:20355727</Xref>
-<Note>(1)H-, (13)C-, (15)N-NMR characterization establishes that the bond is through the C5-carboxyl</Note>
-</ReferenceBlock>
-<Comment>Cross-linking of pup has been established to be through the gamma-carboxyl group of the C-terminal glutamine or glutamic acid.</Comment>
-<Comment>For the modification of a peptidyl glutamic acid by formation of an isopeptide bond through the gamma-carboxyl group to the N2-amino group of a non-peptidyl lysine, see RESID:AA0505.</Comment>
-<Comment>The structure shown in PubChem for this name is incorrect, being instead alpha-(gamma-glutamyl)-lysine, which is not the product of peptide transamidation.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>protein-glutamine gamma-glutamyltransferase (EC 2.3.2.13)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode link="GLN">
-<SequenceSpec>K, Q</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>GO:0003810</Xref>
-<Xref>GO:0018153</Xref>
-<Xref>PSI-MOD:00133</Xref>
-</SequenceCode>
-<SequenceCode link="GLU">
-<SequenceSpec>E, K</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:01484</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>isopeptide bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__isoglutamyl lysine isopeptide (gln-lys) (interchain with k-__q" link="GLN">CROSSLNK Isoglutamyl lysine isopeptide (Gln-Lys) (interchain with K-...)</Feature>
-<Feature type="UniProt" key="crosslnk__isoglutamyl lysine isopeptide (glu-lys) (interchain with k-__e" link="GLU">CROSSLNK Isoglutamyl lysine isopeptide (Glu-Lys) (interchain with K-...)</Feature>
-<Feature type="UniProt" key="crosslnk__isoglutamyl lysine isopeptide (lys-gln)__k__q" link="GLN">CROSSLNK Isoglutamyl lysine isopeptide (Lys-Gln)</Feature>
-<Feature type="UniProt" key="crosslnk__isoglutamyl lysine isopeptide (lys-gln) (interchain with q-__k" link="GLN">CROSSLNK Isoglutamyl lysine isopeptide (Lys-Gln) (interchain with Q-...)</Feature>
-<Feature type="UniProt" key="crosslnk__isoglutamyl lysine isopeptide (lys-glu) (interchain with e-__k" link="GLU">CROSSLNK Isoglutamyl lysine isopeptide (Lys-Glu) (interchain with E-...)</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="crosslnk__glutamyl lysine isopeptide (gln-lys) (interchain with k-__q" link="GLN">CROSSLNK Glutamyl lysine isopeptide (Gln-Lys) (interchain with K-...)</Feature>
-<Note>this UniProt feature is used when it has not been determined whether the linkage is through the alpha- or gamma-carboxyl group</Note>
-</FeatureNote>
-<FeatureNote>
-<Feature type="UniProt" key="crosslnk__glutamyl lysine isopeptide (glu-lys) (interchain with k-__e" link="GLU">CROSSLNK Glutamyl lysine isopeptide (Glu-Lys) (interchain with K-...)</Feature>
-<Note>this UniProt feature is used when it has not been determined whether the linkage is through the alpha- or gamma-carboxyl group</Note>
-</FeatureNote>
-<FeatureNote>
-<Feature type="UniProt" key="crosslnk__glutamyl lysine isopeptide (lys-gln) (interchain with q-__k" link="GLN">CROSSLNK Glutamyl lysine isopeptide (Lys-Gln) (interchain with Q-...)</Feature>
-<Note>this UniProt feature is used when it has not been determined whether the linkage is through the alpha- or gamma-carboxyl group</Note>
-</FeatureNote>
-<FeatureNote>
-<Feature type="UniProt" key="crosslnk__glutamyl lysine isopeptide (lys-glu) (interchain with e-__k" link="GLU">CROSSLNK Glutamyl lysine isopeptide (Lys-Glu) (interchain with E-...)</Feature>
-<Note>this UniProt feature is used when it has not been determined whether the linkage is through the alpha- or gamma-carboxyl group</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0124.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0124.PDB" />
-</Entry>
-<Entry id="AA0125">
-<Header>
-<Code>AA0125</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Sep-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6-(glycyl)-L-lysine</Name>
-<AlternateName>N6-glycyllysine</AlternateName>
-<SystematicName>(2S)-2-amino-6-[(aminoacetyl)amino]hexanoic acid</SystematicName>
-<Xref>CAS:191-22-6</Xref>
-<Xref>ChEBI:21885</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 8 H 14 N 3 O 2</Formula>
-<Weight type="chemical">184.22</Weight>
-<Weight type="physical">184.108602</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0008 AA0012">
-<Formula>C 0 H -2 N 0 O -1</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Vierstra, R.D.</Author>
-<Author>Langan, S.M.</Author>
-<Author>Schaller, G.E.</Author>
-</Authors>
-<Citation>Biochemistry 25, 3105-3108, 1986</Citation>
-<Title>Complete amino acid sequence of ubiquitin from the higher plant Avena sativa.</Title>
-<Xref>DOI:10.1021/bi00359a006</Xref>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>G, K</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Condition>cross-link 2</Condition>
-<Xref>GO:0018276</Xref>
-<Xref>PSI-MOD:00134</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>isopeptide bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__glycyl lysine isopeptide (gly-lys) (interchain with k-__g">CROSSLNK Glycyl lysine isopeptide (Gly-Lys) (interchain with K-...)</Feature>
-<Feature type="UniProt" key="crosslnk__glycyl lysine isopeptide (lys-gly) (interchain with g-cter__k">CROSSLNK Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter ...)</Feature>
-</Features>
-<Image src="/images/AA0125.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0125.PDB" />
-</Entry>
-<Entry id="AA0126">
-<Header>
-<Code>AA0126</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>01-Mar-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-(L-isoaspartyl)-glycine</Name>
-<AlternateName>2-amino-N4-(carboxymethyl)-butanediamic acid</AlternateName>
-<AlternateName>isoaspartyl glycine</AlternateName>
-<AlternateName>N-beta-aspartylglycine</AlternateName>
-<AlternateName>N4-(carboxymethyl)-asparagine</AlternateName>
-<SystematicName>(2S)-2-amino-4-(carboxymethyl)amino-4-oxobutanoic acid</SystematicName>
-<Xref>CAS:3790-52-1</Xref>
-<Xref>ChEBI:21479</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 7 N 2 O 3</Formula>
-<Weight type="chemical">155.13</Weight>
-<Weight type="physical">155.045667</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0003 AA0008" label="ASN">
-<Formula>C 0 H -3 N -1 O 0</Formula>
-<Weight type="chemical">-17.03</Weight>
-<Weight type="physical">-17.026549</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0004 AA0008" label="ASP">
-<Formula>C 0 H -2 N 0 O -1</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wyss, D.F.</Author>
-<Author>Lahm, H.W.</Author>
-<Author>Manneberg, M.</Author>
-<Author>Labhardt, A.M.</Author>
-</Authors>
-<Citation>J. Antibiot. 44, 172-180, 1991</Citation>
-<Title>Anantin -- a peptide antagonist of the atrial natriuretic factor (ANF). II. Determination of the primary sequence by NMR on the basis of proton assignments.</Title>
-<Xref>PMID:1826288</Xref>
-<Note>(1)H-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Knappe, T.A.</Author>
-<Author>Linne, U.</Author>
-<Author>Zirah, S.</Author>
-<Author>Rebuffat, S.</Author>
-<Author>Xie, X.</Author>
-<Author>Marahiel, M.A.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 130, 11446-11454, 2008</Citation>
-<Title>Isolation and structural characterization of capistruin, a lasso peptide predicted from the genome sequence of Burkholderia thailandensis E264.</Title>
-<Xref>DOI:10.1021/ja802966g</Xref>
-<Xref>PMID:18671394</Xref>
-<Note>mass spectrometric characterization and (1)H-NMR identification; gene sequence and biosynthetic studies establish that aspartic acid is activated by ATP to form the isopeptide bond</Note>
-</ReferenceBlock>
-<Comment>For the "lariat" or "lasso" cross-link between glycine and glutamic acid, see RESID:AA0360.</Comment>
-<GeneratingEnzyme>
-<EnzymeName link="ASP">capistruin synthase, beta-aspartyl-glycine cyclo-ligase CapC (EC 6.3.3.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode link="ASN">
-<SequenceSpec>G, N</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Condition>cross-link 2</Condition>
-<Xref>GO:0018264</Xref>
-<Xref>PSI-MOD:00135</Xref>
-</SequenceCode>
-<SequenceCode link="ASP">
-<SequenceSpec>D, G</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:01805</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-<Keyword>isopeptide bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__isoaspartyl glycine isopeptide (gly-asn)__g__n" link="ASN">CROSSLNK Isoaspartyl glycine isopeptide (Gly-Asn)</Feature>
-<Feature type="UniProt" key="crosslnk__isoaspartyl glycine isopeptide (gly-asp)__g__d" link="ASP">CROSSLNK Isoaspartyl glycine isopeptide (Gly-Asp)</Feature>
-<Feature type="UniProt" key="crosslnk__isoaspartyl glycine isopeptide (asn-gly)__n__g" link="ASN">CROSSLNK Isoaspartyl glycine isopeptide (Asn-Gly)</Feature>
-<Feature type="UniProt" key="crosslnk__isoaspartyl glycine isopeptide (asp-gly)__d__g" link="ASP">CROSSLNK Isoaspartyl glycine isopeptide (Asp-Gly)</Feature>
-</Features>
-<Image src="/images/AA0126.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0126.PDB" />
-</Entry>
-<Entry id="AA0127">
-<Header>
-<Code>AA0127</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Sep-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>pyruvic acid</Name>
-<SystematicName>2-oxopropanoic acid</SystematicName>
-<Xref>CAS:127-17-3</Xref>
-<Xref>COMe:BIM000277</Xref>
-<Xref>PDBHET:PYR</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 3 O 2</Formula>
-<Weight type="chemical">71.06</Weight>
-<Weight type="physical">71.013304</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005" label="CYS">
-<Formula>C 0 H -3 N -1 O 1 S -1</Formula>
-<Weight type="chemical">-33.09</Weight>
-<Weight type="physical">-33.003705</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0016" label="SER">
-<Formula>C 0 H -3 N -1 O 0</Formula>
-<Weight type="chemical">-17.03</Weight>
-<Weight type="physical">-17.026549</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0019" label="TYR">
-<Formula>C -6 H -7 N -1 O 0</Formula>
-<Weight type="chemical">-93.13</Weight>
-<Weight type="physical">-93.057849</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Dixon, H.B.F.</Author>
-<Author>Fields, R.</Author>
-</Authors>
-<Citation>Meth. Enzymol. 25, 409-419, 1972</Citation>
-<Title>Specific modification of NH2-terminal residues by transamination.</Title>
-<Xref>DOI:10.1016/S0076-6879(72)25036-4</Xref>
-<Note>chemical detection and amino terminal release using 1,2-diaminobenzene</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gavaret, J.M.</Author>
-<Author>Cahnmann, H.J.</Author>
-<Author>Nunez, J.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 254, 11218-11222, 1979</Citation>
-<Title>The fate of the &#x201c;lost side chain&#x201d; during thyroid hormonogenesis.</Title>
-<Xref>PMID:500639</Xref>
-<Note>radiolabeling and chemical identification of pyruvate from tyrosine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Li, Q.X.</Author>
-<Author>Dowhan, W.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 263, 11516-11522, 1988</Citation>
-<Title>Structural characterization of Escherichia coli phosphatidylserine decarboxylase.</Title>
-<Xref>PMID:3042771</Xref>
-<Note>chemical conversion to alanine using sodium cyanoborohydride</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gallagher, T.</Author>
-<Author>Rozwarski, D.A.</Author>
-<Author>Ernst, S.R.</Author>
-<Author>Hackert, M.L.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 230, 516-528, 1993</Citation>
-<Title>Refined structure of the pyruvoyl-dependent histidine decarboxylase from Lactobacillus 30a.</Title>
-<Xref>DOI:10.1006/jmbi.1993.1168</Xref>
-<Xref>PMID:8464063</Xref>
-<Note>X-ray diffraction, 2.5 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gallagher, T.</Author>
-<Author>Rozwarski, D.A.</Author>
-<Author>Ernst, S.R.</Author>
-<Author>Hackert, M.L.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, December 1992</Citation>
-<Description>Refined structure of the pyruvoyl-dependent histidine decarboxylase from Lactobacillus 30a.</Description>
-<Xref>PDB:1PYA</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Albert, A.</Author>
-<Author>Dhanaraj, V.</Author>
-<Author>Genschel, U.</Author>
-<Author>Khan, G.</Author>
-<Author>Ramjee, M.K.</Author>
-<Author>Pulido, R.</Author>
-<Author>Sibanda, B.L.</Author>
-<Author>von Delft, F.</Author>
-<Author>Witty, M.</Author>
-<Author>Blundell, T.L.</Author>
-<Author>Smith, A.G.</Author>
-<Author>Abell, C.</Author>
-</Authors>
-<Citation>Nature Struct. Biol. 5, 289-293, 1998</Citation>
-<Title>Crystal structure of aspartate decarboxylase at 2.2 A resolution provides evidence for an ester in protein self-processing.</Title>
-<Xref>DOI:10.1038/nsb0498-289</Xref>
-<Xref>PMID:9546220</Xref>
-<Note>X-ray diffraction, 2.20 angstroms; structure of ester intermediate formed after the N to O acyl shift</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Albert, A.</Author>
-<Author>Dhanaraj, V.</Author>
-<Author>Genschel, U.</Author>
-<Author>Khan, G.</Author>
-<Author>Ramjee, M.K.</Author>
-<Author>Pulido, R.</Author>
-<Author>Sybanda, B.L.</Author>
-<Author>Vondelf, F.</Author>
-<Author>Witty, M.</Author>
-<Author>Blundell, T.L.</Author>
-<Author>Smith, A.G.</Author>
-<Author>Abell, C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, October 1997</Citation>
-<Description>Pyruvoyl dependent aspartate decarboxylase.</Description>
-<Xref>PDB:1AW8</Xref>
-<Note>X-ray diffraction, 2.00 angstroms; evidence is presented for partial presence of the ester formed after the N to O acyl shift</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kabisch, U.C.</Author>
-<Author>Graentzdoerffer, A.</Author>
-<Author>Schierhorn, A.</Author>
-<Author>Ruecknagel, K.P.</Author>
-<Author>Andreesen, J.R.</Author>
-<Author>Pich, A.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 274, 8445-8454, 1999</Citation>
-<Title>Identification of D-proline reductase from clostridium sticklandii as a selenoenzyme and indications for a catalytically active pyruvoyl group derived from a cysteine residue by cleavage of a proprotein.</Title>
-<Xref>DOI:10.1074/jbc.274.13.8445</Xref>
-<Xref>PMID:10085076</Xref>
-<Note>mass spectrometric and chemical characterization</Note>
-</ReferenceBlock>
-<Comment>The pyruvic acid forming an amide bond between its 1-carboxyl group and an amino terminal residue arises from oxidative deamination of an encoded amino acid, either cysteine or serine. It is important to distinguish this modification from an exogenous pyruvic acid forming a ketimine bond with its 2-keto group and an amino terminal residue (see RESID:AA0274 and RESID:AA0275).</Comment>
-<SequenceCode link="CYS">
-<SequenceSpec>C</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0018058</Xref>
-<Xref>GO:0018387</Xref>
-<Xref>PSI-MOD:00136</Xref>
-<Xref>PSI-MOD:01154</Xref>
-</SequenceCode>
-<SequenceCode link="SER">
-<SequenceSpec>S</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0018058</Xref>
-<Xref>GO:0018387</Xref>
-<Xref>PSI-MOD:00807</Xref>
-<Xref>PSI-MOD:01154</Xref>
-</SequenceCode>
-<SequenceCode link="TYR">
-<SequenceSpec>Y</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>PSI-MOD:01661</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__pyruvic acid (cys)__c" link="CYS">MOD_RES Pyruvic acid (Cys)</Feature>
-<Feature type="UniProt" key="mod_res__pyruvic acid (ser)__s" link="SER">MOD_RES Pyruvic acid (Ser)</Feature>
-<Feature type="UniProt" key="mod_res__pyruvic acid (tyr)__y" link="TYR">MOD_RES Pyruvic acid (Tyr)</Feature>
-</Features>
-<Image src="/images/AA0127.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0127.PDB" />
-</Entry>
-<Entry id="AA0128">
-<Header>
-<Code>AA0128</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Sep-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-3-phenyllactic acid</Name>
-<SystematicName>(2S)-2-hydroxy-3-phenylpropanoic acid</SystematicName>
-<Xref>CAS:20312-36-1</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 9 O 2</Formula>
-<Weight type="chemical">149.17</Weight>
-<Weight type="physical">149.060255</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0014">
-<Formula>C 0 H -1 N -1 O 1</Formula>
-<Weight type="chemical">0.98</Weight>
-<Weight type="physical">0.984016</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Grimmelikhuijzen, C.J.P.</Author>
-<Author>Rinehart, K.L.</Author>
-<Author>Jacob, E.</Author>
-<Author>Graff, D.</Author>
-<Author>Reinscheid, R.K.</Author>
-<Author>Nothacker, H.P.</Author>
-<Author>Staley, A.L.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 87, 5410-5414, 1990</Citation>
-<Title>Isolation of L-3-phenyllactyl-Leu-Arg-Asn-NH2 (Antho-RNamide), a sea anemone neuropeptide containing an unusual amino-terminal blocking group.</Title>
-<Xref>DOI:10.1073/pnas.87.14.5410</Xref>
-<Xref>PMID:1973541</Xref>
-<Note>mass spectrometric and (1)H-NMR identification; chromatographic stereochemical characterization; chemical synthesis</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>F</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0018058</Xref>
-<Xref>GO:0018061</Xref>
-<Xref>PSI-MOD:00137</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__3-phenyllactic acid__f">MOD_RES 3-phenyllactic acid</Feature>
-</Features>
-<Image src="/images/AA0128.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0128.PDB" />
-</Entry>
-<Entry id="AA0129">
-<Header>
-<Code>AA0129</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>25-Feb-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>2-oxobutanoic acid</Name>
-<AlternateName>2-ketobutyric acid</AlternateName>
-<AlternateName>2-oxobutyric acid</AlternateName>
-<SystematicName>2-oxobutanoic acid</SystematicName>
-<Xref>CAS:600-18-0</Xref>
-<Xref>ChEBI:30831</Xref>
-<Xref>PDBHET:2KT</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 5 O 2</Formula>
-<Weight type="chemical">85.08</Weight>
-<Weight type="physical">85.028954</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0017">
-<Formula>C 0 H -3 N -1 O 0</Formula>
-<Weight type="chemical">-17.03</Weight>
-<Weight type="physical">-17.026549</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kaletta, C.</Author>
-<Author>Entian, K.D.</Author>
-<Author>Kellner, R.</Author>
-<Author>Jung, G.</Author>
-<Author>Reis, M.</Author>
-<Author>Sahl, H.G.</Author>
-</Authors>
-<Citation>Arch. Microbiol. 152, 16-19, 1989</Citation>
-<Title>Pep5, a new lantibiotic: structural gene isolation and prepeptide sequence.</Title>
-<Xref>DOI:10.1007/BF00447005</Xref>
-<Xref>PMID:2764678</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Weil, H.P.</Author>
-<Author>Beck-Sickinger, A.G.</Author>
-<Author>Metzger, J.</Author>
-<Author>Stevanovic, S.</Author>
-<Author>Jung, G.</Author>
-<Author>Josten, M.</Author>
-<Author>Sahl, H.G.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 194, 217-223, 1990</Citation>
-<Title>Biosynthesis of the lantibiotic Pep5. Isolation and characterization of a prepeptide containing dehydroamino acids.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1990.tb19446.x</Xref>
-<Xref>PMID:2253617</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Martin, N.I.</Author>
-<Author>Sprules, T.</Author>
-<Author>Carpenter, M.R.</Author>
-<Author>Cotter, P.D.</Author>
-<Author>Hill, C.</Author>
-<Author>Ross, R.P.</Author>
-<Author>Vederas, J.C.</Author>
-</Authors>
-<Citation>Biochemistry 43, 3049-3056, 2004</Citation>
-<Title>Structural characterization of lacticin 3147, a two-peptide lantibiotic with synergistic activity.</Title>
-<Xref>DOI:10.1021/bi0362065</Xref>
-<Xref>PMID:15023056</Xref>
-<Note>chemical method for removing the amino terminal block</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>T</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0018058</Xref>
-<Xref>GO:0018278</Xref>
-<Xref>PSI-MOD:00138</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__2-oxobutanoic acid__t">MOD_RES 2-oxobutanoic acid</Feature>
-</Features>
-<Image src="/images/AA0129.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0129.PDB" />
-</Entry>
-<Entry id="AA0130">
-<Header>
-<Code>AA0130</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Jun-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N2-succinyl-L-tryptophan</Name>
-<AlternateName>(2S)-2-amino-(6,7-dihydro-6,7-dioxo-1H-indole)-3-propanoic acid</AlternateName>
-<SystematicName>(2S)-2-(3-carboxypropanoyl)amino-3-(1H-indol-3-yl)propanoic acid</SystematicName>
-<Xref>CAS:514803-26-0</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 15 H 15 N 2 O 4</Formula>
-<Weight type="chemical">287.29</Weight>
-<Weight type="physical">287.103182</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0018">
-<Formula>C 4 H 4 N 0 O 3</Formula>
-<Weight type="chemical">100.07</Weight>
-<Weight type="physical">100.016044</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Chan, W.C.</Author>
-<Author>Bycroft, B.W.</Author>
-<Author>Leyland, M.L.</Author>
-<Author>Lian, L.Y.</Author>
-<Author>Roberts, G.C.K.</Author>
-</Authors>
-<Citation>Biochem. J. 291, 23-27, 1993</Citation>
-<Title>A novel post-translational modification of the peptide antibiotic subtilin: isolation and characterization of a natural variant from Bacillus subtilis A.T.C.C. 6633.</Title>
-<Xref>PMID:8471040</Xref>
-<Note>mass spectrometric, (1)H-NMR, and (13)C-NMR identification; chemical synthesis</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>W</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0018062</Xref>
-<Xref>PSI-MOD:00139</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n2-succinyltryptophan__w">MOD_RES N2-succinyltryptophan</Feature>
-</Features>
-<Image src="/images/AA0130.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0130.PDB" />
-</Entry>
-<Entry id="AA0131">
-<Header>
-<Code>AA0131</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Sep-2008</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-phycocyanobilin-L-cysteine</Name>
-<AlternateName>(2R,3R)-3-[(1R)-1-(((2R)-2-amino-2-carboxy)ethylsulfanyl)ethyl]-18-ethyl-1,2,3,19,21,22,24-heptahydro-2,7,13,17-tetramethyl-1,19-dioxo-(21H,22H,24H)-bilin-8,12-dipropanoic acid</AlternateName>
-<AlternateName>PCB</AlternateName>
-<AlternateName>phycobilin cysteine</AlternateName>
-<AlternateName>phycocyanobilin cysteine adduct</AlternateName>
-<SystematicName>(2R,3R)-3-[(1R)-1-(((2R)-2-amino-2-carboxy)ethylsulfanyl)ethyl]-8,12-bis(2-carboxyethyl)-18-ethyl-2,7,13,17-tetramethyl-1,2,3,19,21,22,24-heptahydrobilin-1,19(21H,22H,24H)-dione</SystematicName>
-<Xref>CAS:20298-86-6</Xref>
-<Xref>ChEBI:15617</Xref>
-<Xref>COMe:BIM000148</Xref>
-<Xref>PDBHET:CYC</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 36 H 43 N 5 O 7 S 1</Formula>
-<Weight type="chemical">689.83</Weight>
-<Weight type="physical">689.288320</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 33 H 38 N 4 O 6 S 0</Formula>
-<Weight type="chemical">586.69</Weight>
-<Weight type="physical">586.279135</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Nagy, J.O.</Author>
-<Author>Bishop, J.E.</Author>
-<Author>Klotz, A.V.</Author>
-<Author>Glazer, A.N.</Author>
-<Author>Rapoport, H.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 260, 4864-4868, 1985</Citation>
-<Title>Bilin attachment sites in the alpha, beta, and gamma subunits of R-phycoerythrin. Structural studies on singly and doubly linked phycourobilins.</Title>
-<Xref>PMID:3838747</Xref>
-<Note>mass spectrometric and (1)H-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Moss, G.P.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 178, 277-328, 1988</Citation>
-<Title>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN). Nomenclature of tetrapyrroles. Recommendations 1986.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1988.tb14453.x</Xref>
-<Xref>PMID:3208761</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Szalontai, B.</Author>
-<Author>Gombos, Z.</Author>
-<Author>Csizmadia, V.</Author>
-<Author>Bagyinka, C.</Author>
-<Author>Lutz, M.</Author>
-</Authors>
-<Citation>Biochemistry 33, 11823-11832, 1994</Citation>
-<Title>Structure and interactions of phycocyanobilin chromophores in phycocyanin and allophycocyanin from an analysis of their resonance Raman spectra.</Title>
-<Xref>DOI:10.1021/bi00205a019</Xref>
-<Xref>PMID:7918400</Xref>
-<Note>raman spectroscopy of covalently bound (14)N and (15)N isotopic chromophores</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Stec, B.</Author>
-<Author>Troxler, R.F.</Author>
-<Author>Teeter, M.M.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, June 1995</Citation>
-<Description>Structure of phycocyanin from Cyanidium caldarium at 1.65A resolution.</Description>
-<Xref>PDB:1PHN</Xref>
-<Note>X-ray diffraction, 1.65 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Shen, G.</Author>
-<Author>Saunee, N.A.</Author>
-<Author>Williams, S.R.</Author>
-<Author>Gallo, E.F.</Author>
-<Author>Schluchter, W.M.</Author>
-<Author>Bryant, D.A.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 281, 17768-17778, 2006</Citation>
-<Title>Identification and characterization of a new nlass of bilin lyase: the cpcT gene encodes a bilin lyase responsible for attachment of phycocyanobilin to Cys-153 on the beta-subunit of phycocyanin in Synechococcus sp. PCC 7002.</Title>
-<Xref>DOI:10.1074/jbc.M602563200</Xref>
-<Xref>PMID:16644722</Xref>
-</ReferenceBlock>
-<Comment>A second linkage, an ester between a serine and one of the propanoic acid groups, was reported at one time but was not confirmed. A second cysteine linkage has also been reported to a moiety thought to be phycocyanobilin.</Comment>
-<Comment>The phycocyanobilins transmit blue.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>phycocyanobilin lyase (EC 4.4.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>GO:0017009</Xref>
-<Xref>GO:0018353</Xref>
-<Xref>PSI-MOD:00140</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chromoprotein</Keyword>
-<Keyword>phycocyanobilin</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="binding__phycocyanobilin chromophore (covalent; via 1 link)__c">BINDING Phycocyanobilin chromophore (covalent; via 1 link)</Feature>
-</Features>
-<Image src="/images/AA0131.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0131.PDB" />
-</Entry>
-<Entry id="AA0132">
-<Header>
-<Code>AA0132</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>30-Jun-2005</StrucRevDate>
-<TextChngDate>30-Sep-2008</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-phycoerythrobilin-L-cysteine</Name>
-<AlternateName>18-ethenyl-3-[1-((2-amino-2-carboxy)ethylsulfanyl)ethyl]-2,3,15,16-tetrahydro-2,7,13,17-tetramethyl-1,19-dioxo-(21H,22H,24H)-bilin-8,12-dipropanoic acid</AlternateName>
-<AlternateName>PEB</AlternateName>
-<AlternateName>phycoerythrobilin cysteine adduct</AlternateName>
-<SystematicName>(2S,3R,16R)-18-ethenyl-3-[(1R)-1-(((2R)-2-amino-2-carboxy)ethylsulfanyl)ethyl]-8,12-bis(2-carboxyethyl)-2,7,13,17-tetramethyl-2,3,15,16-tetrahydrobilin-1,19(21H,22H,24H)-dione</SystematicName>
-<Xref>CAS:18097-67-1</Xref>
-<Xref>ChEBI:15618</Xref>
-<Xref>COMe:BIM000147</Xref>
-<Xref>PDBHET:PEB</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 36 H 43 N 5 O 7 S 1</Formula>
-<Weight type="chemical">689.83</Weight>
-<Weight type="physical">689.288320</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 33 H 38 N 4 O 6 S 0</Formula>
-<Weight type="chemical">586.69</Weight>
-<Weight type="physical">586.279135</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Nagy, J.O.</Author>
-<Author>Bishop, J.E.</Author>
-<Author>Klotz, A.V.</Author>
-<Author>Glazer, A.N.</Author>
-<Author>Rapoport, H.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 260, 4864-4868, 1985</Citation>
-<Title>Bilin attachment sites in the alpha, beta, and gamma subunits of R-phycoerythrin. Structural studies on singly and doubly linked phycourobilins.</Title>
-<Xref>PMID:3838747</Xref>
-<Note>mass spectrometric and (1)H-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Moss, G.P.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 178, 277-328, 1988</Citation>
-<Title>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN). Nomenclature of tetrapyrroles. Recommendations 1986.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1988.tb14453.x</Xref>
-<Xref>PMID:3208761</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Chang, W.R.</Author>
-<Author>Jiang, T.</Author>
-<Author>Wan, Z.L.</Author>
-<Author>Zhang, J.P.</Author>
-<Author>Yang, Z.X.</Author>
-<Author>Liang, D.C.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 262, 721-731, 1996</Citation>
-<Title>Crystal structure of R-phycoerythrin from Polysiphonia urceolata at 2.8 angstroms resolution.</Title>
-<Xref>DOI:10.1006/jmbi.1996.0547</Xref>
-<Xref>PMID:8876649</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Liang, D.C.</Author>
-<Author>Jiang, T.</Author>
-<Author>Chang, W.R.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, January 1996</Citation>
-<Description>Crystal structure of R-phycoerythrin from Polysiphonia at 2.8 A resolution.</Description>
-<Xref>PDB:1LIA</Xref>
-</ReferenceBlock>
-<Comment>See the comment for S-phycocyanobilin-L-cysteine (RESID:AA0131). There is an additional chiral center at C-16.</Comment>
-<Comment>The phytochromobilins and phycoerythrobilins transmit red.</Comment>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>GO:0017011</Xref>
-<Xref>GO:0018168</Xref>
-<Xref>PSI-MOD:00141</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chromoprotein</Keyword>
-<Keyword>phycoerythrobilin</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="binding__phycoerythrobilin chromophore (covalent; via 1 link)__c">BINDING Phycoerythrobilin chromophore (covalent; via 1 link)</Feature>
-</Features>
-<Image src="/images/AA0132.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0132.PDB" />
-</Entry>
-<Entry id="AA0133">
-<Header>
-<Code>AA0133</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-Mar-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-phytochromobilin-L-cysteine</Name>
-<AlternateName>18-ethenyl-3-[1-((2-amino-2-carboxy)ethylsulfanyl)ethyl]-1,2,3,19,22,24-hexahydro-2,7,13,17-tetramethyl-1,19-dioxo-21H-biline-8,12-dipropanoic acid</AlternateName>
-<AlternateName>phytochrome chromophore</AlternateName>
-<AlternateName>phytochromobilin cysteine adduct</AlternateName>
-<SystematicName>(2R,3R)-3-[(1R)-1-(((2R)-2-amino-2-carboxy)ethylsulfanyl)ethyl]-8,12-bis(2-carboxyethyl)-18-ethyl-2,7,13,17-tetramethyl-1,2,3,19,21,22,24-heptahydrobilin-1,19(21H,22H,24H)-dione</SystematicName>
-<Xref>CAS:143392-71-6</Xref>
-<Xref>ChEBI:15619</Xref>
-<Xref>COMe:BIM000255</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 36 H 41 N 5 O 7 S 1</Formula>
-<Weight type="chemical">687.81</Weight>
-<Weight type="physical">687.272670</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 33 H 36 N 4 O 6 S 0</Formula>
-<Weight type="chemical">584.67</Weight>
-<Weight type="physical">584.263485</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lagarias, J.C.</Author>
-<Author>Rapoport, H.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 102, 4821-4828, 1980</Citation>
-<Title>Chromopeptides from phytochrome. The structure and linkage of the P(R) form of the phytochrome chromophore.</Title>
-<Xref>DOI:10.1021/ja00534a042</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ruediger, W.</Author>
-<Author>Thuemmler, F.</Author>
-<Author>Cmiel, E.</Author>
-<Author>Schneider, S.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 80, 6244-6248, 1983</Citation>
-<Title>Chromophore structure of the physiologically active form (P(fr)) of phytochrome.</Title>
-<Xref>DOI:10.1073/pnas.80.20.6244</Xref>
-<Xref>PMID:16593380</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Moss, G.P.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 178, 277-328, 1988</Citation>
-<Title>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN). Nomenclature of tetrapyrroles. Recommendations 1986.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1988.tb14453.x</Xref>
-<Xref>PMID:3208761</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Cornejo, J.</Author>
-<Author>Beale, S.I.</Author>
-<Author>Terry, M.J.</Author>
-<Author>Lagarias, J.C.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 267, 14790-14798, 1992</Citation>
-<Title>Phytochrome assembly. The structure and biological activity of 2(R),3(E)-phytochromobilin derived from phycobiliproteins.</Title>
-<Xref>PMID:1634523</Xref>
-</ReferenceBlock>
-<Comment>The phytochromobilins and phycoerythrobilins transmit red.</Comment>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>GO:0017012</Xref>
-<Xref>GO:0018358</Xref>
-<Xref>PSI-MOD:00142</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chromoprotein</Keyword>
-<Keyword>phytochromobilin</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="binding__phytochromobilin chromophore (covalent; via 1 link)__c">BINDING Phytochromobilin chromophore (covalent; via 1 link)</Feature>
-</Features>
-<Image src="/images/AA0133.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0133.PDB" />
-</Entry>
-<Entry id="AA0134">
-<Header>
-<Code>AA0134</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-Dec-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>heme-bis-L-cysteine</Name>
-<AlternateName>2,4-bis[1-(S-cysteinyl)ethyl]protoporphyrin IX</AlternateName>
-<AlternateName>biscysteinyl heme</AlternateName>
-<SystematicName>(7,12-bis[(1S)-1-([(2R)-2-amino-2-carboxyethyl]sulfanyl)ethyl]-3,8,13,17-tetramethyl-21H,23H-porphine-2,18-bis[2-carboxyethyl]-N21,N22,N23,N24)-ferrate</SystematicName>
-<Xref>CAS:14875-96-8</Xref>
-<Xref>ChEBI:17627</Xref>
-<Xref>COMe:BIM000241</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 40 Fe 1 H 42 N 6 O 6 S 2</Formula>
-<Weight type="chemical">822.78</Weight>
-<Weight type="physical">822.195663</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005">
-<Formula>C 34 Fe 1 H 32 N 4 O 4 S 0</Formula>
-<Weight type="chemical">616.50</Weight>
-<Weight type="physical">616.177293</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Dickerson, R.E.</Author>
-<Author>Takano, T.</Author>
-<Author>Eisenberg, D.</Author>
-<Author>Kallai, O.B.</Author>
-<Author>Samson, L.</Author>
-<Author>Cooper, A.</Author>
-<Author>Margoliash, E.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 246, 1511-1535, 1971</Citation>
-<Title>Ferricytochrome c. I. General features of the horse and bonito proteins at 2.8 A resolution.</Title>
-<Xref>PMID:5545094</Xref>
-<Note>X-ray diffraction, 2.8 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gans, P.</Author>
-<Author>Simorre, J.P.</Author>
-<Author>Caffrey, M.</Author>
-<Author>Marion, D.</Author>
-<Author>Richaud, P.</Author>
-<Author>Vermeglio, A.</Author>
-</Authors>
-<Citation>J. Biochem. 119, 1131-1142, 1996</Citation>
-<Title>Sequential 1H and 15N NMR resonance assignment and secondary structure of ferrocytochrome c2 from Rhodobacter sphaeroides.</Title>
-<Xref>PMID:8827449</Xref>
-<Note>(1)H-NMR and (15)N-NMR characterization; conformation of residues 22-145</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Allen, J.W.</Author>
-<Author>Tomlinson, E.J.</Author>
-<Author>Hong, L.</Author>
-<Author>Ferguson, S.J.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 277, 33559-33563, 2002</Citation>
-<Title>The Escherichia coli cytochrome c maturation (Ccm) system does not detectably attach heme to single cysteine variants of an apocytochrome c.</Title>
-<Xref>DOI:10.1074/jbc.M204963200</Xref>
-<Xref>PMID:12048216</Xref>
-<Note>evidence that a disulfide bond is transiently present in apocytochrome c prior to heme attachment</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>holocytochrome-c synthase (EC 4.4.1.17)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C, C</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>GO:0018063</Xref>
-<Xref>GO:0018379</Xref>
-<Xref>PSI-MOD:00143</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chromoprotein</Keyword>
-<Keyword>heme</Keyword>
-<Keyword>iron</Keyword>
-<Keyword>metalloprotein</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="binding__heme (covalent)__c">BINDING Heme (covalent)</Feature>
-</Features>
-<Image src="/images/AA0134.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0134.PDB" />
-</Entry>
-<Entry id="AA0135">
-<Header>
-<Code>AA0135</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>01-Mar-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>heme-L-cysteine</Name>
-<AlternateName>4-[1-(S-cysteinyl)ethyl]protoporphyrin IX</AlternateName>
-<AlternateName>cysteinyl heme</AlternateName>
-<SystematicName>(12-ethenyl-7-[(1S)-1-([(2R)-2-amino-2-carboxyethyl]sulfanyl)ethyl]-3,8,13,17-tetramethyl-21H,23H-porphine-2,18-bis[2-carboxyethyl]-N21,N22,N23,N24)-ferrate</SystematicName>
-<Xref>CAS:14875-96-8</Xref>
-<Xref>ChEBI:17627</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 37 Fe 1 H 37 N 5 O 5 S 1</Formula>
-<Weight type="chemical">719.64</Weight>
-<Weight type="physical">719.186478</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 34 Fe 1 H 32 N 4 O 4 S 0</Formula>
-<Weight type="chemical">616.50</Weight>
-<Weight type="physical">616.177293</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Pettigrew, G.W.</Author>
-<Author>Leaver, J.L.</Author>
-<Author>Meyer, T.E.</Author>
-<Author>Ryle, A.P.</Author>
-</Authors>
-<Citation>Biochem. J. 147, 291-302, 1975</Citation>
-<Title>Purification, properties and amino acid sequence of atypical cytochrome c from two protozoa, Euglena gracilis and Crithidia oncopelti.</Title>
-<Xref>PMID:170910</Xref>
-<Note>chemical and spectrographic characterization; it is uncertain whether the cysteine is linked through the 7-vinyl (as indicated) or through the 12-vinyl group</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mukai, K.</Author>
-<Author>Yoshida, M.</Author>
-<Author>Toyosaki, H.</Author>
-<Author>Yao, Y.</Author>
-<Author>Wakabayashi, S.</Author>
-<Author>Matsubara, H.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 178, 649-656, 1989</Citation>
-<Title>An atypical heme-binding structure of cytochrome c1 of Euglena gracilis mitochondrial complex III.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1989.tb14494.x</Xref>
-<Xref>PMID:2536325</Xref>
-<Note>chemical and spectrographic characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Miller, M.J.</Author>
-<Author>Rapoport, H.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 99, 3479-3485, 1977</Citation>
-<Title>Porphyrin-protein bond of cytochrome c558 from Euglena gracilis.</Title>
-<Xref>DOI:10.1021/ja00452a048</Xref>
-<Xref>PMID:192772</Xref>
-<Note>chemical characterization; the linkage is established to be through the 7-ethenyl group</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yu, J.</Author>
-<Author>Le Brun, N.E.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 273, 8860-8866, 1998</Citation>
-<Title>Studies of the cytochrome subunits of menaquinone:cytochrome c reductase (bc complex) of Bacillus subtilis. Evidence for the covalent attachment of heme to the cytochrome b subunit.</Title>
-<Xref>DOI:10.1074/jbc.273.15.8860</Xref>
-<Xref>PMID:9535866</Xref>
-<Note>chemical characterization; demonstration of an unusual covalent heme attachment in a cytochrome b</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ginger, M.L.</Author>
-<Author>Sam, K.A.</Author>
-<Author>Allen, J.W.</Author>
-</Authors>
-<Citation>Biochem. J. 448, 253-260, 2012</Citation>
-<Title>Probing why trypanosomes assemble atypical cytochrome c with an AxxCH haem-binding motif instead of CxxCH.</Title>
-<Xref>DOI:10.1042/BJ20120757</Xref>
-<Xref>PMID:22928879</Xref>
-<Note>attchment of heme to atypical AXXCH motifs in trypanosome mitochondrial cytochromes</Note>
-</ReferenceBlock>
-<Comment>The stereochemistry of the 7-alpha carbon has not been determined. The S form is shown.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>holocytochrome-c synthase (EC 4.4.1.17)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>GO:0018063</Xref>
-<Xref>GO:0018378</Xref>
-<Xref>PSI-MOD:00144</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chromoprotein</Keyword>
-<Keyword>heme</Keyword>
-<Keyword>iron</Keyword>
-<Keyword>metalloprotein</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="binding__heme (covalent; via 1 link)__c">BINDING Heme (covalent; via 1 link)</Feature>
-</Features>
-<Image src="/images/AA0135.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0135.PDB" />
-</Entry>
-<Entry id="AA0136">
-<Header>
-<Code>AA0136</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>01-Mar-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>tetrakis-L-cysteinyl iron</Name>
-<SystematicName>tetrakis(cysteinato-kappaS)-iron</SystematicName>
-<Xref>COMe:BIM000027</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 12 Fe 1 H 16 N 4 O 4 S 4</Formula>
-<FormalCharge>2-</FormalCharge>
-<Weight type="chemical">464.37</Weight>
-<Weight type="physical">463.941474</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005 AA0005 AA0005">
-<Formula>C 0 Fe 1 H -4 N 0 O 0 S 0</Formula>
-<FormalCharge>2-</FormalCharge>
-<Weight type="chemical">51.81</Weight>
-<Weight type="physical">51.904735</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Watenpaugh, K.D.</Author>
-<Author>Siecker, L.C.</Author>
-<Author>Herriott, J.R.</Author>
-<Author>Jensen, L.H.</Author>
-</Authors>
-<Citation>Acta Crystallogr. B 29, 943-956, 1973</Citation>
-<Title>Refinement of the model of a protein: rubredoxin at 1.5 angstrom resolution.</Title>
-<Xref>DOI:10.1107/S0567740873003675</Xref>
-<Note>X-ray diffraction, 1.5 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Day, M.W.</Author>
-<Author>Hsu, B.T.</Author>
-<Author>Joshua-Tor, L.</Author>
-<Author>Park, J.B.</Author>
-<Author>Zhou, Z.H.</Author>
-<Author>Adams, M.W.W.</Author>
-<Author>Rees, D.C.</Author>
-</Authors>
-<Citation>Protein Sci. 1, 1494-1507, 1992</Citation>
-<Title>X-ray crystal structures of the oxidized and reduced forms of the rubredoxin from the marine hyperthermophilic archaebacterium Pyrococcus furiosus.</Title>
-<Xref>DOI:10.1002/pro.5560011111</Xref>
-<Xref>PMID:1303768</Xref>
-<Note>X-ray diffraction, 1.8 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Day, M.W.</Author>
-<Author>Hsu, B.T.</Author>
-<Author>Joshua-Tor, L.</Author>
-<Author>Park, J.B.</Author>
-<Author>Zhou, Z.H.</Author>
-<Author>Adams, M.W.W.</Author>
-<Author>Rees, D.C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, May 1992</Citation>
-<Description>X-ray crystal structures of the oxidized and reduced forms of the rubredoxin from the marine hyperthermophilic archaebacterium Pyrococcus furiosus.</Description>
-<Xref>PDB:1CAA</Xref>
-<Note>X-ray diffraction, 1.80 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Day, M.W.</Author>
-<Author>Hsu, B.T.</Author>
-<Author>Joshua-Tor, L.</Author>
-<Author>Park, J.B.</Author>
-<Author>Zhou, Z.H.</Author>
-<Author>Adams, M.W.W.</Author>
-<Author>Rees, D.C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, May 1992</Citation>
-<Description>X-ray crystal structures of the oxidized and reduced forms of the rubredoxin from the marine hyperthermophilic archaebacterium Pyrococcus furiosus.</Description>
-<Xref>PDB:1CAD</Xref>
-<Note>X-ray diffraction, 1.80 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Meyer, J.</Author>
-<Author>Gagnon, J.</Author>
-<Author>Sieker, L.C.</Author>
-<Author>Van Dorsselaer, A.</Author>
-<Author>Moulis, J.M.</Author>
-</Authors>
-<Citation>Biochem. J. 271, 839-841, 1990</Citation>
-<Title>Rubredoxin from Clostridium thermosaccharolyticum. Amino acid sequence, mass-spectrometric and preliminary crystallographic data.</Title>
-<Xref>PMID:2244884</Xref>
-<Note>mass spectrometric detection</Note>
-</ReferenceBlock>
-<Comment>The stabilization of Fe(3+) by protein in tetrakis-S-cysteinyliron in the oxidized state can be regarded as a model for formation of the simplest iron-sulfur cluster. The formal charge of the reduced state, Fe(2+), is used for the mass calculation.</Comment>
-<SequenceCode>
-<SequenceSpec>C, C, C, C</SequenceSpec>
-<Condition>cross-link 4</Condition>
-<Xref>GO:0018284</Xref>
-<Xref>PSI-MOD:00145</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>iron</Keyword>
-<Keyword>metalloprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="metal__iron__c">METAL Iron</Feature>
-</Features>
-<Image src="/images/AA0136.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0136.PDB" />
-</Entry>
-<Entry id="AA0137">
-<Header>
-<Code>AA0137</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>01-Mar-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>tetrakis-L-cysteinyl diiron disulfide</Name>
-<SystematicName>tetrakiscysteinato-1kappa(2)S,2kappa(2)S-di-mu-sulfido-diiron</SystematicName>
-<Xref>COMe:BIM000055</Xref>
-<Xref>PDBHET:FES</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 12 Fe 2 H 16 N 4 O 4 S 6</Formula>
-<FormalCharge>2-</FormalCharge>
-<Weight type="chemical">584.34</Weight>
-<Weight type="physical">583.820553</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005 AA0005 AA0005">
-<Formula>C 0 Fe 2 H -4 N 0 O 0 S 2</Formula>
-<FormalCharge>2-</FormalCharge>
-<Weight type="chemical">171.78</Weight>
-<Weight type="physical">171.783814</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Tsukihara, T.</Author>
-<Author>Fukuyama, K.</Author>
-<Author>Nakamura, M.</Author>
-<Author>Katsube, Y.</Author>
-<Author>Tanaka, N.</Author>
-<Author>Kakudo, M.</Author>
-<Author>Wada, K.</Author>
-<Author>Hase, T.</Author>
-<Author>Matsubara, H.</Author>
-</Authors>
-<Citation>J. Biochem. 90, 1763-1773, 1981</Citation>
-<Title>X-Ray analysis of a [2Fe-2S] ferredoxin from Spirulina platensis. Main chain fold and location of side chains at 2.5 angstroms resolution.</Title>
-<Xref>PMID:6801028</Xref>
-<Note>X-ray diffraction, 2.5 angstroms; the spelling of "Tsukihira, T." in the PubMed citation is corrected</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Tsukihara, T.</Author>
-<Author>Fukuyama, K.</Author>
-<Author>Mizushima, M.</Author>
-<Author>Harioka, T.</Author>
-<Author>Kusunoki, M.</Author>
-<Author>Katsube, Y.</Author>
-<Author>Hase, T.</Author>
-<Author>Matsubara, H.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 216, 399-410, 1990</Citation>
-<Title>Structure of the [2Fe-2S] ferredoxin I from the blue-green alga Aphanothece sacrum at 2.2 angstroms resolution.</Title>
-<Xref>DOI:10.1016/S0022-2836(05)80330-4</Xref>
-<Xref>PMID:2123937</Xref>
-<Note>X-ray diffraction, 2.2 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Pochapsky, T. C.</Author>
-<Author>Ye, X. M.</Author>
-<Author>Ratnaswamy, G.</Author>
-<Author>Lyons, T. A.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, July 1994</Citation>
-<Description>An NMR-derived model for the solution structure of oxidized putidaredoxin, a 2-Fe, 2-S ferredoxin from Pseudomonas.</Description>
-<Xref>PDB:1PUT</Xref>
-<Note>NMR</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Petillot, Y.</Author>
-<Author>Golinelli, M.P.</Author>
-<Author>Forest, E.</Author>
-<Author>Meyer, J.</Author>
-</Authors>
-<Citation>Biochem. Biophys. Res. Commun. 210, 686-694, 1995</Citation>
-<Title>Electrospray-ionization mass spectrometry of molecular variants of a [2Fe-2S] ferredoxin.</Title>
-<Xref>DOI:10.1006/bbrc.1995.1714</Xref>
-<Xref>PMID:7763242</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Golinelli, M.P.</Author>
-<Author>Akin, L.A.</Author>
-<Author>Crouse, B.R.</Author>
-<Author>Johnson, M.K.</Author>
-<Author>Meyer, J.</Author>
-</Authors>
-<Citation>Biochemistry 35, 8995-9002, 1996</Citation>
-<Title>Cysteine ligand swapping on a deletable loop of the [2Fe-2S] ferredoxin from Clostridium pasteurianum.</Title>
-<Xref>DOI:10.1021/bi9604284</Xref>
-<Xref>PMID:8688437</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Frolow, F.</Author>
-<Author>Harel, M.</Author>
-<Author>Sussman, J.L.</Author>
-<Author>Shoham, M.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, April 1996</Citation>
-<Description>2Fe-2S Ferredoxin from Haloarcula marismortui.</Description>
-<Xref>PDB:1DOI</Xref>
-<Note>X-ray diffraction, 1.9 angstroms</Note>
-</ReferenceBlock>
-<Comment>See also RESID:AA0225.</Comment>
-<SequenceCode>
-<SequenceSpec>C, C, C, C</SequenceSpec>
-<Condition>cross-link 4</Condition>
-<Xref>GO:0018285</Xref>
-<Xref>PSI-MOD:00146</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>2Fe-2S</Keyword>
-<Keyword>iron-sulfur protein</Keyword>
-<Keyword>metalloprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="metal__iron-sulfur (2fe-2s)__c">METAL Iron-sulfur (2Fe-2S)</Feature>
-<Feature type="UniProt" key="metal__iron-sulfur (2fe-2s); shared with dimeric partner__c">METAL Iron-sulfur (2Fe-2S); shared with dimeric partner</Feature>
-</Features>
-<Image src="/images/AA0137.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0137.PDB" />
-</Entry>
-<Entry id="AA0138">
-<Header>
-<Code>AA0138</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-2005</StrucRevDate>
-<TextChngDate>31-May-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>hexakis-L-cysteinyl triiron trisulfide</Name>
-<AlternateName>tri-mu-sulfidotris(biscysteinato-kappaS-iron)</AlternateName>
-<SystematicName>tri-mu-sulfido-hexakiscysteinato-1kappa(2)S,2kappa(2)S,3kappa(2)S-triiron</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 18 Fe 3 H 24 N 6 O 6 S 9</Formula>
-<FormalCharge>3-</FormalCharge>
-<Weight type="chemical">876.50</Weight>
-<Weight type="physical">875.730830</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005 AA0005 AA0005 AA0005 AA0005">
-<Formula>C 0 Fe 3 H -6 N 0 O 0 S 3</Formula>
-<FormalCharge>3-</FormalCharge>
-<Weight type="chemical">257.67</Weight>
-<Weight type="physical">257.675721</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Stout, C.D.</Author>
-<Author>Ghosh, D.</Author>
-<Author>Pattabhi, V.</Author>
-<Author>Robbins, A.H.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 255, 1797-1800, 1980</Citation>
-<Title>Iron-sulfur clusters in Azotobacter ferredoxin at 2.5 A resolution.</Title>
-<Xref>PMID:7354058</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>George, D.G.</Author>
-<Author>Hunt, L.T.</Author>
-<Author>Yeh, L.S.</Author>
-<Author>Barker, W.C.</Author>
-</Authors>
-<Citation>J. Mol. Evol. 22, 20-31, 1985</Citation>
-<Title>New perspectives on bacterial ferredoxin evolution.</Title>
-<Xref>DOI:10.1007/BF02105801</Xref>
-<Xref>PMID:3932661</Xref>
-<Note>proposal for a model of a 3Fe-3S cluster</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Stout, C.D.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 263, 9256-9260, 1988</Citation>
-<Title>7-Iron ferredoxin revisited.</Title>
-<Xref>PMID:3379067</Xref>
-<Note>the cluster is identified as being 3Fe-4S</Note>
-</ReferenceBlock>
-<Comment>The three-iron three-sulfur cluster is now thought not to exist except possibly as an intermediate form. See RESID:AA0139 and RESID:AA0140.</Comment>
-<SequenceCode>
-<SequenceSpec>C, C, C, C, C, C</SequenceSpec>
-<Condition>cross-link 6</Condition>
-<Xref>GO:0018286</Xref>
-<Xref>PSI-MOD:00147</Xref>
-</SequenceCode>
-<Source>deprecated</Source>
-<Keywords>
-<Keyword>iron-sulfur protein</Keyword>
-<Keyword>metalloprotein</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this dubious modification is not currently annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0138.GIF" alt="DUMMY.GIF" />
-</Entry>
-<Entry id="AA0139">
-<Header>
-<Code>AA0139</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>tris-L-cysteinyl triiron tetrasulfide</Name>
-<AlternateName>mu3-sulfido tri-mu-sulfido tris-S-L-cysteinyl triiron</AlternateName>
-<AlternateName>tris-L-cysteinyl triiron tetrasulfide C3 cluster</AlternateName>
-<AlternateName>tris-L-cysteinyl triiron tetrasulfide cubane form</AlternateName>
-<AlternateName>tris-L-cysteinyl triiron tetrasulfide cuboid cluster</AlternateName>
-<AlternateName>tris-L-cysteinyl triiron tetrasulfide trigonal cluster</AlternateName>
-<SystematicName>mu3-sulfido-tri-mu-sulfido-triscysteinato-1kappaS,2kappaS,3kappaS-triiron</SystematicName>
-<Xref>COMe:BIM000054</Xref>
-<Xref>PDBHET:F3S</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 9 Fe 3 H 12 N 3 O 3 S 7</Formula>
-<FormalCharge>3-</FormalCharge>
-<Weight type="chemical">602.17</Weight>
-<Weight type="physical">601.698821</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005 AA0005">
-<Formula>C 0 Fe 3 H -3 N 0 O 0 S 4</Formula>
-<FormalCharge>3-</FormalCharge>
-<Weight type="chemical">292.75</Weight>
-<Weight type="physical">292.671267</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Howard, J.B.</Author>
-<Author>Lorsbach, T.W.</Author>
-<Author>Ghosh, D.</Author>
-<Author>Melis, K.</Author>
-<Author>Stout, C.D.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 258, 508-522, 1983</Citation>
-<Title>Structure of Azotobacter vinelandii 7Fe ferredoxin. Amino acid sequence and electron density maps of residues.</Title>
-<Xref>PMID:6848518</Xref>
-<Note>X-ray diffraction, 2 angstroms; 3Fe-4S and 4Fe-4S clusters</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Stout, G.H.</Author>
-<Author>Turley, S.</Author>
-<Author>Sieker, L.C.</Author>
-<Author>Jensen, L.H.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 85, 1020-1022, 1988</Citation>
-<Title>Structure of ferredoxin I from Azotobacter vinelandii.</Title>
-<Xref>DOI:10.1073/pnas.85.4.1020</Xref>
-<Xref>PMID:3422475</Xref>
-<Note>X-ray diffraction, 2.6 angstroms; 3Fe-4S and 4Fe-4S clusters</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Stout, C.D.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, June 1993</Citation>
-<Description>Crystal structures of oxidized and reduced Azotobacter vinelandii ferredoxin at pH 8 and 6.</Description>
-<Xref>PDB:1FDA</Xref>
-<Note>X-ray diffraction, 2.10 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kissinger, C.R.</Author>
-<Author>Sieker, L.C.</Author>
-<Author>Adman, E.T.</Author>
-<Author>Jensen, L.H.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 219, 693-715, 1991</Citation>
-<Title>Refined crystal structure of ferredoxin II from Desulfovibrio gigas at 1.7 A.</Title>
-<Xref>DOI:10.1016/0022-2836(91)90665-S</Xref>
-<Xref>PMID:2056535</Xref>
-<Note>X-ray diffraction, 1.7 angstroms; 3Fe-4S cluster, disulfide and methyl mercaptan (see RESID:AA0101)</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kissinger, C.R.</Author>
-<Author>Sieker, L.C.</Author>
-<Author>Adman, E.T.</Author>
-<Author>Jensen, L.H.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, April 1991</Citation>
-<Description>Refined crystal structure of ferredoxin II from Desulfovibrio gigas at 1.7 A.</Description>
-<Xref>PDB:1FXD</Xref>
-<Note>X-ray diffraction, 1.70 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gorst, C.M.</Author>
-<Author>Yeh, Y.H.</Author>
-<Author>Teng, Q.</Author>
-<Author>Calzolai, L.</Author>
-<Author>Zhou, Z.H.</Author>
-<Author>Adams, M.W.W.</Author>
-<Author>La Mar, G.N.</Author>
-</Authors>
-<Citation>Biochemistry 34, 600-610, 1995</Citation>
-<Title>[1]H NMR investigation of the paramagnetic cluster environment in Pyrococcus furiosus three-iron ferredoxin: sequence-specific assignment of ligated cysteines independent of tertiary structure.</Title>
-<Xref>DOI:10.1021/bi00002a027</Xref>
-<Xref>PMID:7819255</Xref>
-<Note>conformation, binding site, and disulfide bond assignments by (1)H-NMR; this ferredoxin can form a 4Fe-4S cluster but it readily converts to a stable 3Fe-4S cluster</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fujii, T.</Author>
-<Author>Hata, Y.</Author>
-<Author>Oozeki, M.</Author>
-<Author>Moriyama, H.</Author>
-<Author>Wakagi, T.</Author>
-<Author>Tanaka, N.</Author>
-<Author>Oshima, T.</Author>
-</Authors>
-<Citation>Biochemistry 36, 1505-1513, 1997</Citation>
-<Title>The crystal structure of zinc-containing ferredoxin from the thermoacidophilic archaeon Sulfolobus sp. strain 7.</Title>
-<Xref>DOI:10.1021/bi961966j</Xref>
-<Xref>PMID:9063899</Xref>
-<Note>X-ray diffraction, 2.0 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fujii, T.</Author>
-<Author>Hata, Y.</Author>
-<Author>Moriyama, H.</Author>
-<Author>Wakagi, T.</Author>
-<Author>Tanaka, N.</Author>
-<Author>Oshima, T.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, August 1996</Citation>
-<Description>Structure of ferredoxin.</Description>
-<Xref>PDB:1XER</Xref>
-<Note>X-ray diffraction, 2.0 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Goodfellow, B.J.</Author>
-<Author>Macedo, A.L.</Author>
-<Author>Rodrigues, P.</Author>
-<Author>Moura, I.</Author>
-<Author>Wray, V.</Author>
-<Author>Moura, J.J.</Author>
-</Authors>
-<Citation>J. Biol. Inorg. Chem. 4, 421-430, 1999</Citation>
-<Title>The solution structure of a [3Fe-4S] ferredoxin: oxidised ferredoxin II from Desulfovibrio gigas.</Title>
-<Xref>DOI:10.1007/s007750050328</Xref>
-<Xref>PMID:10555576</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Goodfellow, B.J.</Author>
-<Author>Macedo, A.L.</Author>
-<Author>Rodrigues, P.</Author>
-<Author>Wray, V.</Author>
-<Author>Moura, I.</Author>
-<Author>Moura, J.J.G.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, October 1998</Citation>
-<Description>The NMR solution structure of the 3Fe ferredoxin II from Desulfovibrio gigas, 15 structures.</Description>
-<Xref>PDB:1F2G</Xref>
-<Note>COSY, TOCSY, and NOESY NMR spectroscopy</Note>
-</ReferenceBlock>
-<Comment>The activity of some trigonal 3Fe-4S clusters has been questioned. Reconfiguration to linear 3Fe-4S clusters or to 4Fe-4S clusters may occur. See RESID:AA0140 and RESID:AA0326.</Comment>
-<Comment>Observed oxidation states for the ligated cluster are 3-, 4-, and 5-.</Comment>
-<SequenceCode>
-<SequenceSpec>C, C, C</SequenceSpec>
-<Condition>cross-link 3</Condition>
-<Xref>GO:0018287</Xref>
-<Xref>PSI-MOD:00148</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>3Fe-4S</Keyword>
-<Keyword>iron-sulfur protein</Keyword>
-<Keyword>metalloprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="metal__iron-sulfur (3fe-4s)__c">METAL Iron-sulfur (3Fe-4S)</Feature>
-</Features>
-<Image src="/images/AA0139.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0139.PDB" />
-</Entry>
-<Entry id="AA0140">
-<Header>
-<Code>AA0140</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>tetrakis-L-cysteinyl tetrairon tetrasulfide</Name>
-<AlternateName>tetra-mu3-sulfidotetrakis(S-cysteinyliron)</AlternateName>
-<SystematicName>tetra-mu3-sulfido-tetrakis(cysteinato)-1kappaS,2kappaS,3kappaS,4kappaS-tetrahedro-tetrairon</SystematicName>
-<Xref>COMe:BIM000008</Xref>
-<Xref>PDBHET:SF4</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 12 Fe 4 H 16 N 4 O 4 S 8</Formula>
-<FormalCharge>2-</FormalCharge>
-<Weight type="chemical">760.15</Weight>
-<Weight type="physical">759.634570</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005 AA0005 AA0005">
-<Formula>C 0 Fe 4 H -4 N 0 O 0 S 4</Formula>
-<FormalCharge>2-</FormalCharge>
-<Weight type="chemical">347.59</Weight>
-<Weight type="physical">347.597831</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Adman, E.T.</Author>
-<Author>Sieker, L.C.</Author>
-<Author>Jensen, L.H.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 251, 3801-3806, 1976</Citation>
-<Title>Structure of Peptococcus aerogenes ferredoxin. Refinement at 2 angstroms resolution.</Title>
-<Xref>PMID:932007</Xref>
-<Note>X-ray diffraction, 2.0 angstroms; monomer with two 4Fe-4S clusters; the spelling of "Siefker, L.C." in the PubMed citation is corrected</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Backes, G.</Author>
-<Author>Mino, Y.</Author>
-<Author>Loehr, T.M.</Author>
-<Author>Meyer, T.E.</Author>
-<Author>Cusanovich, M.A.</Author>
-<Author>Sweeney, W.V.</Author>
-<Author>Adman, E.T.</Author>
-<Author>Sanders-Loehr, J.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 113, 2055-2064, 1991</Citation>
-<Title>The environment of Fe4S4 clusters in ferredoxins and high-potential iron proteins. New information from x-ray crystallography and resonance Raman spectroscopy.</Title>
-<Xref>DOI:10.1021/ja00006a027</Xref>
-<Note>X-ray diffraction, 2.0 angstroms; Raman spectroscopy; monomer with two 4Fe-4S clusters compared with HiPIP type</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Huber, J.G.</Author>
-<Author>Gaillard, J.</Author>
-<Author>Moulis, J.M.</Author>
-</Authors>
-<Citation>Biochemistry 34, 194-205, 1995</Citation>
-<Title>NMR of Chromatium vinosum ferredoxin: evidence for structural inequivalence and impeded electron transfer between the two [4Fe-4S] clusters.</Title>
-<Xref>DOI:10.1021/bi00001a024</Xref>
-<Xref>PMID:7819196</Xref>
-<Note>conformation by (1)H-NMR and (13)C-NMR; monomer with two 4Fe-4S clusters</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sery, A.</Author>
-<Author>Housset, D.</Author>
-<Author>Serre, L.</Author>
-<Author>Bonicel, J.</Author>
-<Author>Hatchikian, C.</Author>
-<Author>Frey, M.</Author>
-<Author>Roth, M.</Author>
-</Authors>
-<Citation>Biochemistry 33, 15408-15417, 1994</Citation>
-<Title>Crystal structure of the ferredoxin I from Desulfovibrio africanus at 2.3 angstrom resolution.</Title>
-<Xref>DOI:10.1021/bi00255a022</Xref>
-<Xref>PMID:7803404</Xref>
-<Note>X-ray diffraction, 2.3 angstroms; single 4Fe-4S cluster</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fukuyama, K.</Author>
-<Author>Nagahara, Y.</Author>
-<Author>Tsukihara, T.</Author>
-<Author>Katsube, Y.</Author>
-<Author>Hase, T.</Author>
-<Author>Matsubara, H.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 199, 183-193, 1988</Citation>
-<Title>Tertiary structure of Bacillus thermoproteolyticus [4Fe-4S] ferredoxin. Evolutionary implications for bacterial ferredoxins.</Title>
-<Xref>DOI:10.1016/0022-2836(88)90388-9</Xref>
-<Xref>PMID:3351918</Xref>
-<Note>X-ray diffraction, 2.3 angstroms; single 4Fe-4S cluster</Note>
-</ReferenceBlock>
-<Comment>Several different types of 4Fe-4S cluster are observed. Typically two 4Fe-4S clusters are shared in a single domain. Also observed are: one 4Fe-4S cluster and one 3Fe-4S cluster (see RESID:AA0139) in a single domain, a single 4Fe-4S cluster, one 4Fe-4S cluster shared between dimeric partners, and two 4Fe-4S clusters shared between two different chains.</Comment>
-<Comment>Three cysteine ligands may denote that the fourth iron is labile or that it binds another prosthetic group.</Comment>
-<Comment>The oxidation states usually observed for the ligated cluster are 2- and 3-.</Comment>
-<SequenceCode>
-<SequenceSpec>C, C, C, C</SequenceSpec>
-<Condition>cross-link 4</Condition>
-<Xref>GO:0018288</Xref>
-<Xref>PSI-MOD:00149</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>4Fe-4S</Keyword>
-<Keyword>iron-sulfur protein</Keyword>
-<Keyword>metalloprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="metal__iron-sulfur (4fe-4s)__c">METAL Iron-sulfur (4Fe-4S)</Feature>
-<Feature type="UniProt" key="metal__iron-sulfur (4fe-4s); shared with dimeric partner__c">METAL Iron-sulfur (4Fe-4S); shared with dimeric partner</Feature>
-</Features>
-<Image src="/images/AA0140.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0140.PDB" />
-</Entry>
-<Entry id="AA0141">
-<Header>
-<Code>AA0141</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Dec-2011</StrucRevDate>
-<TextChngDate>01-Mar-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-cysteinyl-L-histidino-homocitryl molybdenum heptairon nonasulfide carbide</Name>
-<AlternateName>nitrogenase iron-molybdenum cofactor</AlternateName>
-<SystematicName>cysteinato-8kappaS-histidino-1kappaN(tau)-[(2R)-4-carboxy-2-(carboxymethyl)-2-oxidobutanoate-1kappaO(1),1kappaO(2)]-mu6-carbido-2:3:4:5:6:7kappa(6)C-hexa-mu3-sulfido-1:2:3kappa(3)S;1:2:4kappa(3)S;1:3:4kappa(3)S;5:6:8kappa(3)S;5:7:8kappa(3)S;6:7:8kappa(3)S-tri-mu2-sulfido-2:5kappa(2)S;3:6kappa(2)S;4:7kappa(2)S molybdenum heptairon</SystematicName>
-<Xref>COMe:BIM000057</Xref>
-<Xref>PDBHET:CFM</Xref>
-<Xref>PDBHET:CFN</Xref>
-<Xref>PDBHET:HCA</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 17 Fe 7 H 18 Mo 1 N 4 O 9 S 10</Formula>
-<Weight type="chemical">1229.82</Weight>
-<Weight type="physical">1231.278059</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0009">
-<Formula>C 8 Fe 7 H 6 Mo 1 N 0 O 7 S 9</Formula>
-<Weight type="chemical">989.53</Weight>
-<Weight type="physical">991.209962</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kim, J.</Author>
-<Author>Rees, D.C.</Author>
-</Authors>
-<Citation>Science 257, 1677-1682, 1992</Citation>
-<Title>Structural models for the metal centers in the nitrogenase molybdenum-iron protein.</Title>
-<Xref>DOI:10.1126/science.1529354</Xref>
-<Xref>PMID:1529354</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kim, J.</Author>
-<Author>Rees, D.C.</Author>
-</Authors>
-<Citation>Nature 360, 553-560, 1992</Citation>
-<Title>Crystallographic structure and functional implications of the nitrogenase molybdenum-iron protein from Azotobacter vinelandii.</Title>
-<Xref>DOI:10.1038/360553a0</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ma, L.</Author>
-<Author>Gavini, N.</Author>
-<Author>Liu, H.I.</Author>
-<Author>Hedman, B.</Author>
-<Author>Hodgson, K.O.</Author>
-<Author>Burgess, B.K.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 269, 18007-18015, 1994</Citation>
-<Title>Large scale isolation and characterization of the molybdenum-iron cluster from nitrogenase.</Title>
-<Xref>PMID:8027059</Xref>
-<Note>EPR and X-ray absorption spectrographic analysis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mayer, S.M.</Author>
-<Author>Lawson, D.M.</Author>
-<Author>Gormal, C.A.</Author>
-<Author>Roe, S.M.</Author>
-<Author>Smith, B.E.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 292, 871-891, 1999</Citation>
-<Title>New insights into structure-function relationships in nitrogenase: A 1.6 Angstom resolution X-ray crystallographic study of Klebsiella pneumoniae MoFe-protein.</Title>
-<Xref>DOI:10.1006/jmbi.1999.3107</Xref>
-<Xref>PMID:10525412</Xref>
-<Note>X-ray diffraction, 1.6 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mayer, S.M.</Author>
-<Author>Lawson, D.M.</Author>
-<Author>Gormal, C.A.</Author>
-<Author>Roe, S.M.</Author>
-<Author>Smith, B.E.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, May 1999</Citation>
-<Description>Nitrogenase Mo-Fe protein from Klebsiella pneumoniae, dithionite-reduced state.</Description>
-<Xref>PDB:1QGU</Xref>
-<Note>X-ray diffraction, 1.6 angstroms, reduced form</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Einsle, O.</Author>
-<Author>Tezcan, F.A.</Author>
-<Author>Andrade, S.L.A.</Author>
-<Author>Schmid, B.</Author>
-<Author>Yoshida, M.</Author>
-<Author>Howard, J.B.</Author>
-<Author>Rees, D.C.</Author>
-</Authors>
-<Citation>Science 297, 1696-1700, 2002</Citation>
-<Title>Nitrogenase MoFe-protein at 1.16 A resolution: a central ligand in the FeMo-cofactor.</Title>
-<Xref>DOI:10.1126/science.1073877</Xref>
-<Xref>PMID:12215645</Xref>
-<Note>X-ray diffraction, 1.16 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Einsle, O.</Author>
-<Author>Tezcan, F.A.</Author>
-<Author>Andrade, S.L.A.</Author>
-<Author>Schmid, B.</Author>
-<Author>Yoshida, M.</Author>
-<Author>Howard, J.B.</Author>
-<Author>Rees, D.C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, June 2002</Citation>
-<Description>Nitrogenase MoFe protein from Azotobacter vinelandii.</Description>
-<Xref>PDB:1M1N</Xref>
-<Note>X-ray diffraction, 1.16 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lee, H.I.</Author>
-<Author>Benton, P.M.C.</Author>
-<Author>Laryukhin, M.</Author>
-<Author>Igarashi, R.Y.</Author>
-<Author>Dean, D.R.</Author>
-<Author>Seefeldt, L.C.</Author>
-<Author>Hoffman, B.M.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 125, 5604-5605, 2003</Citation>
-<Title>The interstitial atom of the nitrogenase FeMo-Cofactor: ENDOR and ESEEM show it is not an exchangeable nitrogen.</Title>
-<Xref>DOI:10.1021/ja034383n</Xref>
-<Xref>PMID:12733878</Xref>
-<Note>electron-nuclear double resonance (ENDOR) spectroscopic analysis, and electron spin-echo envelope modulation (ESEEM) spectroscopic analysis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lancaster, K.M.</Author>
-<Author>Roemelt, M.</Author>
-<Author>Ettenhuber, P.</Author>
-<Author>Hu, Y.</Author>
-<Author>Ribbe, M.W.</Author>
-<Author>Neese, F.</Author>
-<Author>Bergmann, U.</Author>
-<Author>DeBeer, S.</Author>
-</Authors>
-<Citation>Science 334, 974-977, 2011</Citation>
-<Title>X-ray emission spectroscopy evidences a central carbon in the nitrogenase iron-molybdenum cofactor.</Title>
-<Xref>DOI:10.1126/science.1206445</Xref>
-<Xref>PMID:22096198</Xref>
-<Note>X-ray emission spectroscopy indicates that the central atom is a C(4-) ion</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Spatzal, T.</Author>
-<Author>Aksoyoglu, M.</Author>
-<Author>Zhang, L.</Author>
-<Author>Andrade, S.L.</Author>
-<Author>Schleicher, E.</Author>
-<Author>Weber, S.</Author>
-<Author>Rees, D.C.</Author>
-<Author>Einsle, O.</Author>
-</Authors>
-<Citation>Science 334, 940, 2011</Citation>
-<Title>Evidence for interstitial carbon in nitrogenase FeMo cofactor.</Title>
-<Xref>DOI:10.1126/science.1214025</Xref>
-<Xref>PMID:22096190</Xref>
-<Note>X-ray diffraction, 1.00 angstroms, and electron spin-echo envelope modulation (ESEEM) spectroscopic analysis with (13)C labeled cofactor</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Spatzal, T.</Author>
-<Author>Einsle, O.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, October 2011</Citation>
-<Description>A. vinelandii nitrogenase MoFe protein at atomic resolution.</Description>
-<Xref>PDB:3U7Q</Xref>
-<Note>X-ray diffraction, 1.00 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wiig, J.A.</Author>
-<Author>Hu, Y.</Author>
-<Author>Lee, C.C.</Author>
-<Author>Ribbe, M.W.</Author>
-</Authors>
-<Citation>Science 337, 1672-1675, 2012</Citation>
-<Title>Radical SAM-dependent carbon insertion into the nitrogenase M-cluster.</Title>
-<Xref>DOI:10.1126/science.1224603</Xref>
-<Xref>PMID:23019652</Xref>
-<Note>the nitrogenase synthase NifB protein is a radical SAM that helps assemble 4Fe-4S clusters and provides the central carbide atom from a SAM with at least one free radical hydrogen abstraction</Note>
-</ReferenceBlock>
-<Comment>Cysteine binds one iron of a 4Fe-3S cluster; the other three irons are connected by three mu(2)-sulfides and one mu(6)-carbon to three irons of a Mo-3Fe-3S cluster; the molybdenum is further bound by the 2-oxide and 2-carboxylate of homocitrate (2-hydroxy-1,2,4-butanetricarboxylic acid) and the pros-N of histidine.</Comment>
-<SequenceCode>
-<SequenceSpec>C, H</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Condition>incidental to RESID:AA0300</Condition>
-<Xref>GO:0018290</Xref>
-<Xref>PSI-MOD:00150</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>iron-sulfur protein</Keyword>
-<Keyword>metalloprotein</Keyword>
-<Keyword>molybdenum</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt" key="metal__molybdenum-iron-sulfur (7fe-mo-9s-x-homocitryl)__c">METAL Molybdenum-iron-sulfur (7Fe-Mo-9S-X-homocitryl)</Feature>
-<Note>these UniProt features have not been revised</Note>
-</FeatureNote>
-<FeatureNote>
-<Feature type="UniProt" key="metal__molybdenum-iron-sulfur (7fe-mo-9s-x-homocitryl); via pros nitrogen__h">METAL Molybdenum-iron-sulfur (7Fe-Mo-9S-X-homocitryl); via pros nitrogen</Feature>
-<Note>these UniProt features have not been revised</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0141.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0141.PDB" />
-</Entry>
-<Entry id="AA0142">
-<Header>
-<Code>AA0142</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>27-Feb-1998</StrucRevDate>
-<TextChngDate>31-May-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-cysteinyl molybdopterin</Name>
-<AlternateName>cysteinyl Mo-molybdopterin</AlternateName>
-<AlternateName>cysteinyl Mo-pterin</AlternateName>
-<AlternateName>molybdoenzyme molybdenum cofactor</AlternateName>
-<SystematicName>(4R,5aR,11aR)-8-amino-2-[(2R)-2-amino-2-carboxyethyl]sulfanyl-4,5a,6,9,10,11,11a-heptahydro-4-(phosphoric acid)methyl-2,2,10-trioxo-pteridino[6,7-5,6]pyrano[3,4-4,3][1,2,5]molybdadithiolene</SystematicName>
-<Xref>CAS:73508-07-3</Xref>
-<Xref>PDBHET:MO</Xref>
-<Xref>PDBHET:MPN</Xref>
-<Xref>PDBHET:MSS</Xref>
-<Xref>PDBHET:MTE</Xref>
-<Xref>PDBHET:MTQ</Xref>
-<Xref>PDBHET:MTV</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 13 H 16 Mo 1 N 6 O 9 P 1 S 3</Formula>
-<Weight type="chemical">623.41</Weight>
-<Weight type="physical">624.893259</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 10 H 11 Mo 1 N 5 O 8 P 1 S 2</Formula>
-<Weight type="chemical">520.27</Weight>
-<Weight type="physical">521.884074</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Chan, M.K.</Author>
-<Author>Mukund, S.</Author>
-<Author>Kletzin, A.</Author>
-<Author>Adams, M.W.W.</Author>
-<Author>Rees, D.C.</Author>
-</Authors>
-<Citation>Science 267, 1463-1469, 1995</Citation>
-<Title>Structure of a hyperthermophilic tungstopterin enzyme, aldehyde ferredoxin oxidoreductase.</Title>
-<Xref>DOI:10.1126/science.7878465</Xref>
-<Xref>PMID:7878465</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kisker, C.</Author>
-<Author>Schindelin, H.</Author>
-<Author>Pacheco, A.</Author>
-<Author>Wehbi, W.A.</Author>
-<Author>Garrett, R.M.</Author>
-<Author>Rajagopalan, K.V.</Author>
-<Author>Enemark, J.H.</Author>
-<Author>Rees, D.C.</Author>
-</Authors>
-<Citation>Cell 91, 973-983, 1997</Citation>
-<Title>Molecular basis of sulfite oxidase deficiency from the structure of sulfite oxidase.</Title>
-<Xref>DOI:10.1016/S0092-8674(00)80488-2</Xref>
-<Xref>PMID:9428520</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Schrader, N.</Author>
-<Author>Fischer, K.</Author>
-<Author>Theis, K.</Author>
-<Author>Mendel, R.R.</Author>
-<Author>Schwarz, G.</Author>
-<Author>Kisker, C.</Author>
-</Authors>
-<Citation>Structure 11, 1251-1263, 2003</Citation>
-<Title>The crystal structure of plant sulfite oxidase provides insights into sulfite oxidation in plants and animals.</Title>
-<Xref>DOI:10.1016/j.str.2003.09.001</Xref>
-<Xref>PMID:14527393</Xref>
-<Note>X-ray diffraction, 2.6 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Schrader, N.</Author>
-<Author>Fischer, K.</Author>
-<Author>Theis, K.</Author>
-<Author>Mendel, R.R.</Author>
-<Author>Schwarz, G.</Author>
-<Author>Kisker, C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, May 2003</Citation>
-<Description>The crystal structure of plant sulfite oxidase provides insight into sulfite oxidation in plants and animals.</Description>
-<Xref>PDB:1OGP</Xref>
-<Note>X-ray diffraction, 2.6 angstroms</Note>
-</ReferenceBlock>
-<Comment>A hydrogenated (+4H) structure is shown. The fully oxidized form would be the corresponding 4,9,10-trihydro form.</Comment>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>GO:0018292</Xref>
-<Xref>PSI-MOD:00151</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>metalloprotein</Keyword>
-<Keyword>molybdenum</Keyword>
-<Keyword>molybdopterin</Keyword>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="metal__molybdenum-pterin__c">METAL Molybdenum-pterin</Feature>
-</Features>
-<Image src="/images/AA0142.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0142.PDB" />
-</Entry>
-<Entry id="AA0143">
-<Header>
-<Code>AA0143</Code>
-<Dates>
-<CreationDate>01-Sep-1995</CreationDate>
-<StrucRevDate>01-Sep-1995</StrucRevDate>
-<TextChngDate>31-May-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-(8alpha-FAD)-L-cysteine</Name>
-<AlternateName>8alpha-(S-cysteinyl)FAD</AlternateName>
-<SystematicName>(2R)-2-amino-3-[8alpha-riboflavin 5'-(trihydrogen diphosphate) 5'-&gt;5'-ester with adenosine]sulfanylpropanoic acid</SystematicName>
-<Xref>COMe:BIM000201</Xref>
-<Xref>PDBHET:FAD</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 30 H 36 N 10 O 16 P 2 S 1</Formula>
-<Weight type="chemical">886.68</Weight>
-<Weight type="physical">886.150669</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 27 H 31 N 9 O 15 P 2 S 0</Formula>
-<Weight type="chemical">783.54</Weight>
-<Weight type="physical">783.141485</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wagner, M.A.</Author>
-<Author>Khanna, P.</Author>
-<Author>Jorns, M.S.</Author>
-</Authors>
-<Citation>Biochemistry 38, 5588-5595, 1999</Citation>
-<Title>Structure of the flavocoenzyme of two homologous amine oxidases: monomeric sarcosine oxidase and N-methyltryptophan oxidase.</Title>
-<Xref>DOI:10.1021/bi982955o</Xref>
-<Xref>PMID:10220347</Xref>
-<Note>mass spectrometric and chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Trickey, P.</Author>
-<Author>Wagner, M.A.</Author>
-<Author>Jorns, M.S.</Author>
-<Author>Mathews, F.S.</Author>
-</Authors>
-<Citation>Structure 7, 331-345, 1999</Citation>
-<Title>Monomeric sarcosine oxidase: structure of a covalently flavinylated amine oxidizing enzyme.</Title>
-<Xref>DOI:10.1016/S0969-2126(99)80043-4</Xref>
-<Xref>PMID:10368302</Xref>
-<Note>X-ray diffraction, 1.80 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wagner, M.A.</Author>
-<Author>Trickey, P.</Author>
-<Author>Chen, Z.-W.</Author>
-<Author>Mathews, F.S.</Author>
-<Author>Jorns, M.S.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, March 2000</Citation>
-<Description>Complex of monomeric sarcosine oxidase with the inhibitor dimethylglycine.</Description>
-<Xref>PDB:1EL5</Xref>
-<Note>X-ray diffraction, 1.80 angstroms</Note>
-</ReferenceBlock>
-<Comment>The arrangement of the attachment has not been completely established in some cases.</Comment>
-<Comment>The keyword "phosphoprotein" is not used with flavin modifications linked through the flavin.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>GO:0018294</Xref>
-<Xref>PSI-MOD:00152</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>*phosphoprotein</Keyword>
-<Keyword>FAD</Keyword>
-<Keyword>flavoprotein</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__s-8alpha-fad cysteine__c">MOD_RES S-8alpha-FAD cysteine</Feature>
-</Features>
-<Image src="/images/AA0143.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0143.PDB" />
-</Entry>
-<Entry id="AA0144">
-<Header>
-<Code>AA0144</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>01-Sep-1995</StrucRevDate>
-<TextChngDate>31-Mar-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>3'-(8alpha-FAD)-L-histidine</Name>
-<AlternateName>8alpha-(N(delta)-histidyl)FAD</AlternateName>
-<AlternateName>8alpha-(N3'-histidyl)FAD</AlternateName>
-<AlternateName>8alpha-N1-histidyl FAD [misnomer]</AlternateName>
-<AlternateName>N(pi)-(8alpha-FAD)-histidine</AlternateName>
-<AlternateName>pros-(8alpha-FAD)-histidine</AlternateName>
-<SystematicName>(2S)-2-amino-3-(3-[8alpha-riboflavin 5'-(trihydrogen diphosphate) 5'-&gt;5'-ester with adenosine]imidazol-4-yl)propanoic acid</SystematicName>
-<Xref>COMe:BIM000202</Xref>
-<Xref>PDBHET:FAD</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 33 H 38 N 12 O 16 P 2</Formula>
-<Weight type="chemical">920.68</Weight>
-<Weight type="physical">920.200396</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0009">
-<Formula>C 27 H 31 N 9 O 15 P 2</Formula>
-<Weight type="chemical">783.54</Weight>
-<Weight type="physical">783.141485</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Edmondson, D.E.</Author>
-<Author>Kenney, W.C.</Author>
-<Author>Singer, T.P.</Author>
-</Authors>
-<Citation>Biochemistry 15, 2937-2945, 1976</Citation>
-<Title>Structural elucidation and properties of 8alpha-(N1-histidyl)riboflavin: the flavin component of thiamine dehydrogenase and beta-cyclopiazonate oxidocyclase.</Title>
-<Xref>DOI:10.1021/bi00659a001</Xref>
-<Xref>PMID:8076</Xref>
-<Note>chemical and spectrographic characterization; the authors use biochemical rather than IUPAC numbering</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Malito, E.</Author>
-<Author>Coda, A.</Author>
-<Author>Bilyeu, K.D.</Author>
-<Author>Fraaije, M.W.</Author>
-<Author>Mattevi, A.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 341, 1237-1249, 2004</Citation>
-<Title>Structures of Michaelis and product complexes of plant cytokinin dehydrogenase: implications for flavoenzyme catalysis.</Title>
-<Xref>DOI:10.1016/j.jmb.2004.06.083</Xref>
-<Xref>PMID:15321719</Xref>
-<Note>X-ray diffraction, 1.7 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Malito, E.</Author>
-<Author>Mattevi, A.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, June 2004</Citation>
-<Description>Native cytokinin dehydrogenase.</Description>
-<Xref>PDB:1W1O</Xref>
-<Note>X-ray diffraction, 1.7 angstroms</Note>
-</ReferenceBlock>
-<Comment>The arrangement of the attachment has not been completely established in some cases.</Comment>
-<Comment>The keyword "phosphoprotein" is not used with flavin modifications linked through the flavin.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>H</SequenceSpec>
-<Xref>GO:0018295</Xref>
-<Xref>PSI-MOD:00153</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>*phosphoprotein</Keyword>
-<Keyword>FAD</Keyword>
-<Keyword>flavoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__pros-8alpha-fad histidine__h">MOD_RES Pros-8alpha-FAD histidine</Feature>
-</Features>
-<Image src="/images/AA0144.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0144.PDB" />
-</Entry>
-<Entry id="AA0145">
-<Header>
-<Code>AA0145</Code>
-<Dates>
-<CreationDate>01-Sep-1995</CreationDate>
-<StrucRevDate>01-Sep-1995</StrucRevDate>
-<TextChngDate>31-Mar-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O4'-(8alpha-FAD)-L-tyrosine</Name>
-<AlternateName>8alpha-(O4'-tyrosyl)FAD</AlternateName>
-<SystematicName>(2S)-2-amino-3-(4-[8alpha-riboflavin 5'-(trihydrogen diphosphate) 5'-&gt;5'-ester with adenosine]oxyphenyl)propanoic acid</SystematicName>
-<Xref>COMe:BIM000196</Xref>
-<Xref>PDBHET:FAD</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 36 H 40 N 10 O 17 P 2</Formula>
-<Weight type="chemical">946.72</Weight>
-<Weight type="physical">946.204813</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0019">
-<Formula>C 27 H 31 N 9 O 15 P 2</Formula>
-<Weight type="chemical">783.54</Weight>
-<Weight type="physical">783.141485</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>McIntire, W.</Author>
-<Author>Edmondson, D.E.</Author>
-<Author>Singer, T.P.</Author>
-<Author>Hopper, D.J.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 255, 6553-6555, 1980</Citation>
-<Title>8alpha-O-tyrosyl-FAD: a new form of covalently bound flavin from p-cresol methylhydroxylase.</Title>
-<Xref>PMID:7391034</Xref>
-<Note>chemical and spectrographic characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mathews, F.S.</Author>
-<Author>Chen, Z.W.</Author>
-<Author>Bellamy, H.D.</Author>
-<Author>McIntire, W.S.</Author>
-</Authors>
-<Citation>Biochemistry 30, 238-247, 1991</Citation>
-<Title>Three-dimensional structure of p-cresol methylhydroxylase (flavocytochrome c) from Pseudomonas putida at 3.0-A resolution.</Title>
-<Xref>DOI:10.1021/bi00215a034</Xref>
-<Xref>PMID:1846290</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Cunane, L.M.</Author>
-<Author>Chen, Z.W.</Author>
-<Author>Shamala, N.</Author>
-<Author>Mathews, F.S.</Author>
-<Author>Cronin, C.N.</Author>
-<Author>McIntire, W.S.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, November 1999</Citation>
-<Description>Crystal structure of p-cresol methylhydroxylase at 2.5 A resolution.</Description>
-<Xref>PDB:1DII</Xref>
-<Note>X-ray diffraction, 2.50 angstroms</Note>
-</ReferenceBlock>
-<Comment>The keyword "phosphoprotein" is not used with flavin modifications linked through the flavin.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>Y</SequenceSpec>
-<Xref>GO:0018296</Xref>
-<Xref>PSI-MOD:00154</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>*phosphoprotein</Keyword>
-<Keyword>FAD</Keyword>
-<Keyword>flavoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__o-8alpha-fad tyrosine__y">MOD_RES O-8alpha-FAD tyrosine</Feature>
-</Features>
-<Image src="/images/AA0145.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0145.PDB" />
-</Entry>
-<Entry id="AA0146">
-<Header>
-<Code>AA0146</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-Mar-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-3',4'-dihydroxyphenylalanine</Name>
-<AlternateName>L-3'-hydroxytyrosine</AlternateName>
-<AlternateName>L-DOPA</AlternateName>
-<AlternateName>levodopa</AlternateName>
-<SystematicName>(2S)-2-amino-3-(3,4-dihydroxyphenyl)propanoic acid</SystematicName>
-<Xref>CAS:59-92-7</Xref>
-<Xref>PDBHET:DAH</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 9 N 1 O 3</Formula>
-<Weight type="chemical">179.18</Weight>
-<Weight type="physical">179.058243</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0019">
-<Formula>C 0 H 0 N 0 O 1</Formula>
-<Weight type="chemical">16.00</Weight>
-<Weight type="physical">15.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Waite, J.H.</Author>
-</Authors>
-<Citation>J. Comp. Physiol. B, Biochem. Syst. Environ. Physiol. 156, 491-496, 1986</Citation>
-<Title>Mussel glue from Mytilus californianus Conrad: a comparative study.</Title>
-<Xref>DOI:10.1007/BF00691034</Xref>
-<Xref>PMID:3734192</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Waite, J.H.</Author>
-<Author>Jensen, R.A.</Author>
-<Author>Morse, D.E.</Author>
-</Authors>
-<Citation>Biochemistry 31, 5733-5738, 1992</Citation>
-<Title>Cement precursor proteins of the reef-building polychaete Phragmatopoma californica (Fewkes).</Title>
-<Xref>DOI:10.1021/bi00140a007</Xref>
-<Xref>PMID:1610822</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Waite, J.H.</Author>
-</Authors>
-<Citation>Anal. Biochem. 192, 429-433, 1991</Citation>
-<Title>Detection of peptidyl-3,4-dihydroxyphenylalanine by amino acid analysis and microsequencing techniques.</Title>
-<Xref>DOI:10.1016/0003-2697(91)90560-G</Xref>
-<Xref>PMID:1903612</Xref>
-<Note>chromatographic identification; PTH derivative</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>Y</SequenceSpec>
-<Condition>incidental to RESID:AA0368</Condition>
-<Xref>GO:0018067</Xref>
-<Xref>PSI-MOD:00155</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__3&apos;,4&apos;-dihydroxyphenylalanine__y">MOD_RES 3',4'-dihydroxyphenylalanine</Feature>
-</Features>
-<Image src="/images/AA0146.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0146.PDB" />
-</Entry>
-<Entry id="AA0147">
-<Header>
-<Code>AA0147</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-2',4',5'-topaquinone</Name>
-<AlternateName>2,4,5-trihydroxyphenylalanine quinone</AlternateName>
-<AlternateName>5-(2-carboxy-2-aminoethyl)-2-hydroxy-1,4-benzoquinone</AlternateName>
-<AlternateName>L-2,4,5-TOPAquinone</AlternateName>
-<AlternateName>TPQ</AlternateName>
-<SystematicName>(2S)-2-amino-3-(5-hydroxy-2,5-cyclohexadien-1,4-dion-2-yl)propanoic acid</SystematicName>
-<Xref>ChEBI:21187</Xref>
-<Xref>COMe:BIM000264</Xref>
-<Xref>PDBHET:TPQ</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 7 N 1 O 4</Formula>
-<Weight type="chemical">193.16</Weight>
-<Weight type="physical">193.037508</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0019">
-<Formula>C 0 H -2 N 0 O 2</Formula>
-<Weight type="chemical">29.98</Weight>
-<Weight type="physical">29.974179</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Janes, S.M.</Author>
-<Author>Mu, D.</Author>
-<Author>Wemmer, D.</Author>
-<Author>Smith, A.J.</Author>
-<Author>Kaur, S.</Author>
-<Author>Maltby, D.</Author>
-<Author>Burlingame, A.L.</Author>
-<Author>Klinman, J.P.</Author>
-</Authors>
-<Citation>Science 248, 981-987, 1990</Citation>
-<Title>A new redox cofactor in eukaryotic enzymes: 6-hydroxydopa at the active site of bovine serum amine oxidase.</Title>
-<Xref>DOI:10.1126/science.2111581</Xref>
-<Xref>PMID:2111581</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mu, D.</Author>
-<Author>Janes, S.M.</Author>
-<Author>Smith, A.J.</Author>
-<Author>Brown, D.E.</Author>
-<Author>Dooley, D.M.</Author>
-<Author>Klinman, J.P.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 267, 7979-7982, 1992</Citation>
-<Title>Tyrosine codon corresponds to topa quinone at the active site of copper amine oxidases.</Title>
-<Xref>PMID:1569055</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Janes, S.M.</Author>
-<Author>Palcic, M.M.</Author>
-<Author>Scaman, C.H.</Author>
-<Author>Smith, A.J.</Author>
-<Author>Brown, D.E.</Author>
-<Author>Dooley, D.M.</Author>
-<Author>Mure, M.</Author>
-<Author>Klinman, J.P.</Author>
-</Authors>
-<Citation>Biochemistry 31, 12147-12154, 1992</Citation>
-<Title>Identification of topaquinone and its consensus sequence in copper amine oxidases.</Title>
-<Xref>DOI:10.1021/bi00163a025</Xref>
-<Xref>PMID:1457410</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Murray, J.M.</Author>
-<Author>Saysell, C.G.</Author>
-<Author>Wilmot, C.M.</Author>
-<Author>Tambyrajah, W.S.</Author>
-<Author>Jaeger, J.</Author>
-<Author>Knowles, P.F.</Author>
-<Author>Phillips, S.E.</Author>
-<Author>McPherson, M.J.</Author>
-</Authors>
-<Citation>Biochemistry 38, 8217-8227, 1999</Citation>
-<Title>The active site base controls cofactor reactivity in Escherichia coli amine oxidase: x-ray crystallographic studies with mutational variants.</Title>
-<Xref>DOI:10.1021/bi9900469</Xref>
-<Xref>PMID:10387067</Xref>
-<Note>this modification forms active site Schiff base intermediates with amine substrates</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>Y</SequenceSpec>
-<Xref>GO:0018068</Xref>
-<Xref>PSI-MOD:00156</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>quinoprotein</Keyword>
-<Keyword>topaquinone</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__2&apos;,4&apos;,5&apos;-topaquinone__y">MOD_RES 2',4',5'-topaquinone</Feature>
-</Features>
-<Image src="/images/AA0147.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0147.PDB" />
-</Entry>
-<Entry id="AA0148">
-<Header>
-<Code>AA0148</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Jun-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-tryptophyl quinone</Name>
-<AlternateName>2-amino-3-(6,7-dioxo-6,7-dihydro-1H-indol-3-yl)-propionic acid</AlternateName>
-<AlternateName>3-[(2S)-2-amino-2-carboxyethyl]-6,7-indolinedione</AlternateName>
-<AlternateName>N-(3-carboxy-1-oxopropyl)-L-tryptophan</AlternateName>
-<SystematicName>(2S)-2-amino-3-(6,7-dioxo-1H-indol-3-yl)propanoic acid</SystematicName>
-<Xref>CAS:73205-73-9</Xref>
-<Xref>PDBHET:TRQ</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 11 H 8 N 2 O 3</Formula>
-<Weight type="chemical">216.20</Weight>
-<Weight type="physical">216.053492</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0018">
-<Formula>C 0 H -2 N 0 O 2</Formula>
-<Weight type="chemical">29.98</Weight>
-<Weight type="physical">29.974179</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>McIntire, W.S.</Author>
-<Author>Wemmer, D.E.</Author>
-<Author>Chistoserdov, A.</Author>
-<Author>Lidstrom, M.E.</Author>
-</Authors>
-<Citation>Science 252, 817-824, 1991</Citation>
-<Title>A new cofactor in a prokaryotic enzyme: tryptophan tryptophylquinone as the redox prosthetic group in methylamine dehydrogenase.</Title>
-<Xref>DOI:10.1126/science.2028257</Xref>
-<Xref>PMID:2028257</Xref>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>W</SequenceSpec>
-<Condition>incidental to RESID:AA0149</Condition>
-<Condition>incidental to RESID:AA0313</Condition>
-<Condition>secondary to RESID:AA0521</Condition>
-<Xref>GO:0019926</Xref>
-<Xref>PSI-MOD:00157</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>quinoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__tryptophylquinone__w">MOD_RES Tryptophylquinone</Feature>
-</Features>
-<Image src="/images/AA0148.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0148.PDB" />
-</Entry>
-<Entry id="AA0149">
-<Header>
-<Code>AA0149</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-Dec-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>4-(L-tryptophan-2-yl)-L-tryptophyl quinone</Name>
-<AlternateName>2-amino-3-[2-[2-amino-3-(2-carboxyethyl)-6,7-dioxo-1H-indol-4-yl]-1H-indol-3-yl]propanoic acid</AlternateName>
-<AlternateName>4'-tryptophan-tryptophylquinone</AlternateName>
-<AlternateName>4-(2'-tryptophyl)tryptophan-6,7-dione</AlternateName>
-<AlternateName>alpha,alpha'-diamino-6',7'-dihydro-6',7'-dioxo-(2,4'-bi-1H-indole)-3,3'-dipropanoic acid</AlternateName>
-<AlternateName>TTQ</AlternateName>
-<SystematicName>3-[(2S)-2-amino-2-carboxyethyl]-4-(3-[(2S)-2-amino-2-carboxyethyl]-1H-indol-2-yl)-6,7-indolinedione</SystematicName>
-<Xref>CAS:134645-25-3</Xref>
-<Xref>ChEBI:20251</Xref>
-<Xref>COMe:BIM000262</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 22 H 16 N 4 O 4</Formula>
-<Weight type="chemical">400.39</Weight>
-<Weight type="physical">400.117155</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0018 AA0018">
-<Formula>C 0 H -4 N 0 O 2</Formula>
-<Weight type="chemical">27.97</Weight>
-<Weight type="physical">27.958529</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>McIntire, W.S.</Author>
-<Author>Wemmer, D.E.</Author>
-<Author>Chistoserdov, A.</Author>
-<Author>Lidstrom, M.E.</Author>
-</Authors>
-<Citation>Science 252, 817-824, 1991</Citation>
-<Title>A new cofactor in a prokaryotic enzyme: tryptophan tryptophylquinone as the redox prosthetic group in methylamine dehydrogenase.</Title>
-<Xref>DOI:10.1126/science.2028257</Xref>
-<Xref>PMID:2028257</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Jensen, L.M.</Author>
-<Author>Sanishvili, R.</Author>
-<Author>Davidson, V.L.</Author>
-<Author>Wilmot, C.M.</Author>
-</Authors>
-<Citation>Science 327, 1392-1394, 2010</Citation>
-<Title>In crystallo posttranslational modification within a MauG/pre-methylamine dehydrogenase complex.</Title>
-<Xref>DOI:10.1126/science.1182492</Xref>
-<Xref>PMID:20223990</Xref>
-<Note>X-ray diffraction, 2.1 angstroms; complex of methylamine dehydrogenase with the enzyme forming the modification</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>methylamine dehydrogenase activase MauG (EC 6.-.-.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>W, W</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Condition>secondary to RESID:AA0148</Condition>
-<Xref>GO:0018069</Xref>
-<Xref>PSI-MOD:00158</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>quinoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__tryptophan tryptophylquinone (trp-trp)__w__w">CROSSLNK Tryptophan tryptophylquinone (Trp-Trp)</Feature>
-</Features>
-<Image src="/images/AA0149.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0149.PDB" />
-</Entry>
-<Entry id="AA0150">
-<Header>
-<Code>AA0150</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-phosphopantetheine-L-serine</Name>
-<SystematicName>(2R)-2-hydroxy-3,3-dimethyl-4-[(2S)-2-amino-2-carboxyethyl]phosphonato-N-(3-oxo-3-[(2-sulfanylethyl)amino]propyl)butanamide</SystematicName>
-<Xref>ChEBI:64891</Xref>
-<Xref>PDBHET:PNS</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 14 H 26 N 3 O 8 P 1 S 1</Formula>
-<Weight type="chemical">427.41</Weight>
-<Weight type="physical">427.117822</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 11 H 21 N 2 O 6 P 1 S 1</Formula>
-<Weight type="chemical">340.33</Weight>
-<Weight type="physical">340.085794</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Majerus, P.W.</Author>
-<Author>Alberts, A.W.</Author>
-<Author>Vagelos, P.R.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 240, 4723-4726, 1965</Citation>
-<Title>Acyl carrier protein. VII. The primary structure of the substrate-binding site.</Title>
-<Xref>PMID:5321310</Xref>
-<Note>chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Pugh, E.L.</Author>
-<Author>Wakil, S.J.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 240, 4727-4733, 1965</Citation>
-<Title>Studies on the mechanism of fatty acid synthesis. XIV. The prosthetic group of acyl carrier protein and the mode of its attachment to the protein.</Title>
-<Xref>PMID:5321311</Xref>
-<Note>chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Roncari, D.A.</Author>
-<Author>Bradshaw, R.A.</Author>
-<Author>Vagelos, P.R.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 247, 6234-6242, 1972</Citation>
-<Title>Acyl carrier protein. XIX. Amino acid sequence of liver fatty acid synthetase peptides containing 4'-phosphopantetheine.</Title>
-<Xref>PMID:4568609</Xref>
-<Note>radioisotope labeling</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ehmann, D.E.</Author>
-<Author>Gehring, A.M.</Author>
-<Author>Walsh, C.T.</Author>
-</Authors>
-<Citation>Biochemistry 38, 6171-6177, 1999</Citation>
-<Title>Lysine biosynthesis in Saccharomyces cerevisiae: mechanism of alpha-aminoadipate reductase (Lys2) involves posttranslational phosphopantetheinylation by Lys5.</Title>
-<Xref>DOI:10.1021/bi9829940</Xref>
-<Xref>PMID:10320345</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Parris, K.D.</Author>
-<Author>Lin, L.</Author>
-<Author>Tam, A.</Author>
-<Author>Mathew, R.</Author>
-<Author>Hixon, J.</Author>
-<Author>Stahl, M.</Author>
-<Author>Fritz, C.C.</Author>
-<Author>Seehra, J.</Author>
-<Author>Somers, W.S.</Author>
-</Authors>
-<Citation>Structure 8, 883-895, 2000</Citation>
-<Title>Crystal structures of substrate binding to Bacillus subtilis holo-(acyl carrier protein) synthase reveal a novel trimeric arrangement of molecules resulting in three active sites.</Title>
-<Xref>DOI:10.1016/S0969-2126(00)00178-7</Xref>
-<Xref>PMID:10997907</Xref>
-<Note>X-ray diffraction, 2.3 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Parris, K.D.</Author>
-<Author>Lin, L.</Author>
-<Author>Tam, A.</Author>
-<Author>Mathew, R.</Author>
-<Author>Hixon, J.</Author>
-<Author>Stahl, M.</Author>
-<Author>Fritz, C.C.</Author>
-<Author>Seehra, J.</Author>
-<Author>Somers, W.S.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, June 2000</Citation>
-<Description>Holo-(acyl carrier protein) synthase in complex with holo-(acyl carrier protein).</Description>
-<Xref>PDB:1F80</Xref>
-<Note>X-ray diffraction, 2.3 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Roujeinikova, A.</Author>
-<Author>Baldock, C.</Author>
-<Author>Simon, W.J.</Author>
-<Author>Gilroy, J.</Author>
-<Author>Baker, P.J.</Author>
-<Author>Stuitje, A.R.</Author>
-<Author>Rice, D.W.</Author>
-<Author>Slabas, A.R.</Author>
-<Author>Rafferty, J.B.</Author>
-</Authors>
-<Citation>Structure 10, 825-835, 2002</Citation>
-<Title>X-ray crystallographic studies on butyryl-ACP reveal flexibility of the structure around a putative acyl chain binding site.</Title>
-<Xref>DOI:10.1016/S0969-2126(02)00775-X</Xref>
-<Xref>PMID:12057197</Xref>
-<Note>X-ray diffraction, 1.2 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Roujeinikova, A.</Author>
-<Author>Baldock, C.</Author>
-<Author>Simon, W.J.</Author>
-<Author>Gilroy, J.</Author>
-<Author>Baker, P.J.</Author>
-<Author>Stuitje, A.R.</Author>
-<Author>Rice, D.W.</Author>
-<Author>Slabas, A.R.</Author>
-<Author>Rafferty, J.B.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, February 2002</Citation>
-<Description>Crystal structure of butyryl-ACP I62M mutant.</Description>
-<Xref>PDB:1L0I</Xref>
-<Note>X-ray diffraction, 1.2 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Raychaudhuri, S.</Author>
-<Author>Rajasekharan, R.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 278, 37648-37657, 2003</Citation>
-<Title>Nonorganellar acyl carrier protein from oleaginous yeast is a homologue of ribosomal protein P2.</Title>
-<Xref>DOI:10.1074/jbc.M305052200</Xref>
-<Xref>PMID:12869567</Xref>
-<Note>radioisotope labeling and mass spectrometric identification; this protein does not have homology with acyl carrier protein, and many homologs of this protein are not modified by phosphopantetheine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Dorrestein, P.C.</Author>
-<Author>Bumpus, S.B.</Author>
-<Author>Calderone, C.T.</Author>
-<Author>Garneau-Tsodikova, S.</Author>
-<Author>Aron, Z.D.</Author>
-<Author>Straight, P.D.</Author>
-<Author>Kolter, R.</Author>
-<Author>Walsh, C.T.</Author>
-<Author>Kelleher, N.L.</Author>
-</Authors>
-<Citation>Biochemistry 45, 12756-12766, 2006</Citation>
-<Title>Facile detection of acyl and peptidyl intermediates on thiotemplate carrier domains via phosphopantetheinyl elimination reactions during tandem mass spectrometry.</Title>
-<Xref>DOI:10.1021/bi061169d</Xref>
-<Xref>PMID:17042494</Xref>
-<Note>mass spectrometric analysis with detection with detection of phosphoserine after secondary neutral loss of pantetheine</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>holo-[acyl-carrier-protein] synthase (EC 2.7.8.7)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>GO:0018070</Xref>
-<Xref>PSI-MOD:00159</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>phosphopantetheine</Keyword>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__o-(pantetheine 4'-phosphoryl)serine__s">MOD_RES O-(pantetheine 4'-phosphoryl)serine</Feature>
-</Features>
-<Image src="/images/AA0150.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0150.PDB" />
-</Entry>
-<Entry id="AA0151">
-<Header>
-<Code>AA0151</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>26-May-2006</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N4-(N-acetylamino)glucosyl-L-asparagine</Name>
-<AlternateName>N4-(2-acetamido-2-deoxy-beta-D-glucopyranosyl)-L-asparagine</AlternateName>
-<AlternateName>N4-(2-acetylamino-2-deoxy-beta-D-glucopyranosyl)-L-asparagine</AlternateName>
-<AlternateName>N4-(N-acetylglucosaminyl)asparagine</AlternateName>
-<AlternateName>N4-asparagine-beta-N-acetylglucosaminide</AlternateName>
-<AlternateName>N4-glycosyl-L-asparagine</AlternateName>
-<AlternateName>N4-glycosylasparagine</AlternateName>
-<SystematicName>(2S)-2-amino-4-(2-acetamido-2-deoxy-beta-D-glucopyranosyl)amino-4-oxobutanoic acid</SystematicName>
-<Xref>CAS:10036-64-3</Xref>
-<Xref>CAS:2776-93-4</Xref>
-<Xref>ChEBI:132248</Xref>
-<Xref>PDBHET:NAG</Xref>
-<Xref>PDBHET:NDG</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 12 H 19 N 3 O 7 +</Formula>
-<Weight type="chemical">317.30 +</Weight>
-<Weight type="physical">317.122300 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0003">
-<Formula>C 8 H 13 N 1 O 5 +</Formula>
-<Weight type="chemical">203.19 +</Weight>
-<Weight type="physical">203.079373 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Baker, J.R.</Author>
-<Author>Cifonelli, J.A.</Author>
-<Author>Rodén, L.</Author>
-</Authors>
-<Citation>Biochem. J. 115, 11P, 1969</Citation>
-<Title>The linkage of corneal keratosulphate to protein.</Title>
-<Xref>PMID:4242854</Xref>
-<Note>chemical characterization of keratan sulfate linkage to protein</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hunt, L.T.</Author>
-<Author>Dayhoff, M.O.</Author>
-</Authors>
-<Citation>Biochem. Biophys. Res. Commun. 39, 757-765, 1970</Citation>
-<Title>The occurrence in proteins of the tripeptides Asn-X-Ser and Asn-X-Thr and of bound carbohydrate.</Title>
-<Xref>DOI:10.1016/0006-291X(70)90270-6</Xref>
-<Xref>PMID:5490222</Xref>
-<Note>recognition of glycosylation motif</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bergman, L.W.</Author>
-<Author>Kuehl, W.M.</Author>
-</Authors>
-<Citation>Biochemistry 16, 4490-4497, 1977</Citation>
-<Title>Addition of glucosamine and mannose to nascent immunoglobulin heavy chains.</Title>
-<Xref>DOI:10.1021/bi00639a025</Xref>
-<Xref>PMID:410438</Xref>
-<Note>demonstration that in mammals N-glycosylation is a co-translational process; modification can begin before peptide release from the ribosome</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kehry, M.</Author>
-<Author>Sibley, C.</Author>
-<Author>Fuhrman, J.</Author>
-<Author>Schilling, J.</Author>
-<Author>Hood, L.E.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 76, 2932-2936, 1979</Citation>
-<Title>Amino acid sequence of a mouse immunoglobulin mu chain.</Title>
-<Xref>DOI:10.1073/pnas.76.6.2932</Xref>
-<Xref>PMID:111247</Xref>
-<Note>glycosylation at an N-G-G-T site</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Miletich, J.P.</Author>
-<Author>Broze Jr., G.J.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 265, 11397-11404, 1990</Citation>
-<Title>Beta protein C is not glycosylated at asparagine 329. The rate of translation may influence the frequency of usage at asparagine-X-cysteine sites.</Title>
-<Xref>PMID:1694179</Xref>
-<Note>partial glycosylation at an N-X-C site</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lizak, C.</Author>
-<Author>Gerber, S.</Author>
-<Author>Numao, S.</Author>
-<Author>Aebi, M.</Author>
-<Author>Locher, K.P.</Author>
-</Authors>
-<Citation>Nature 474, 350-355, 2011</Citation>
-<Title>X-ray structure of a bacterial oligosaccharyltransferase.</Title>
-<Xref>DOI:10.1038/nature10151</Xref>
-<Xref>PMID:21677752</Xref>
-<Note>X-ray diffraction, 3.40 angstroms; detail of sequon interaction with active site</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lizak, C.</Author>
-<Author>Gerber, S.</Author>
-<Author>Numao, S.</Author>
-<Author>Aebi, M.</Author>
-<Author>Locher, K.P.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, March 2011</Citation>
-<Description>Bacterial oligosaccharyltransferase PglB.</Description>
-<Xref>PDB:3RCE</Xref>
-<Note>X-ray diffraction, 3.40 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Matczuk, A.K.</Author>
-<Author>Kunec, D.</Author>
-<Author>Veit, M.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 288, 35396-35405, 2013</Citation>
-<Title>Co-translational processing of glycoprotein 3 from equine arteritis virus: N-glycosylation adjacent to the signal peptide prevents cleavage.</Title>
-<Xref>DOI:10.1074/jbc.M113.505420</Xref>
-<Xref>PMID:24142700</Xref>
-<Note>the sequence NNTT can be efficiently glycosylated on both asparagines, and N-glycosylation can block signal peptide processing</Note>
-</ReferenceBlock>
-<Comment>This modification typically occurs in extracellar peptides with an NX[ST] motif. Partial modification has been observed to occur with cysteine, rather than serine or threonine, in the third position. Secondary structure features are important, and proline in the second or fourth positions inhibits modification.</Comment>
-<Comment>See also RESID:AA0420 and RESID:AA0421 for other N4-glycosylated asparagines.</Comment>
-<Comment>The PDB has some entries with asparagine apparently alpha-glycosylated with N-acetylglucosamine, those with PDBHET:NDG. These are low resolution structures and appear to be erroneous.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>dolichyl-diphosphooligosaccharide-protein glycotransferase (EC 2.4.1.119)</EnzymeName>
-<EnzymeName>protein N-acetylglucosaminyltransferase (EC 2.4.1.94)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>N</SequenceSpec>
-<Xref>GO:0006487</Xref>
-<Xref>GO:0018279</Xref>
-<Xref>PSI-MOD:00831</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__n-linked (glcnac) asparagine__n">CARBOHYD N-linked (GlcNAc) asparagine</Feature>
-<Feature type="UniProt" key="carbohyd__n-linked (glcnac or glcnac...) asparagine__n">CARBOHYD N-linked (GlcNAc or GlcNAc...) asparagine</Feature>
-<Feature type="UniProt" key="carbohyd__n-linked (glcnac...) asparagine__n">CARBOHYD N-linked (GlcNAc...) asparagine</Feature>
-<Feature type="UniProt" key="carbohyd__n-linked (glcnac...) (keratan sulfate) asparagine__n">CARBOHYD N-linked (GlcNAc...) (keratan sulfate) asparagine</Feature>
-<Feature type="UniProt" key="carbohyd__n-linked (glcnac...) (polylactosaminoglycan) asparagine__n">CARBOHYD N-linked (GlcNAc...) (polylactosaminoglycan) asparagine</Feature>
-</Features>
-<Image src="/images/AA0151.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0151.PDB" />
-</Entry>
-<Entry id="AA0152">
-<Header>
-<Code>AA0152</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>02-Dec-2005</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-glucosyl-L-cysteine</Name>
-<AlternateName>S-(beta-D-glucopyranosyl)cysteine</AlternateName>
-<AlternateName>S-glycosyl-cysteine</AlternateName>
-<SystematicName>(2R)-2-amino-3-[(beta-D-glucopyranosyl)sulfanyl]propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 15 N 1 O 6 S 1 +</Formula>
-<Weight type="chemical">265.28 +</Weight>
-<Weight type="physical">265.062008 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 6 H 10 N 0 O 5 S 0 +</Formula>
-<Weight type="chemical">162.14 +</Weight>
-<Weight type="physical">162.052823 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Weiss, J.B.</Author>
-<Author>Lote, C.J.</Author>
-<Author>Bobinski, H.</Author>
-</Authors>
-<Citation>Nature New Biol. 234, 25-26, 1971</Citation>
-<Title>New low molecular weight glycopeptide containing triglucosylcysteine in human erythrocyte membrane.</Title>
-<Xref>DOI:10.1038/newbio234025a0</Xref>
-<Xref>PMID:5286858</Xref>
-<Note>chromatographic detection and chemical characterization; S-triglucosylcysteine peptide; the peptide was not isolated or characterized in subsequent work, and the reported peptide sequence has not been found in the human proteome</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Elsayed, S.</Author>
-<Author>Bennich, H.</Author>
-</Authors>
-<Citation>Scand. J. Immunol. 4, 203-208, 1975</Citation>
-<Title>The primary structure of allergen M from cod.</Title>
-<Xref>DOI:10.1111/j.1365-3083.1975.tb02618.x</Xref>
-<Xref>PMID:1145128</Xref>
-<Note>chromatographic detection and chemical characterization; S-glucosylcysteine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Olsen, E.H.</Author>
-<Author>Rahbek-Nielsen, H.</Author>
-<Author>Thogersen, I.B.</Author>
-<Author>Roepstorff, P.</Author>
-<Author>Enghild, J.J.</Author>
-</Authors>
-<Citation>Biochemistry 37, 408-416, 1998</Citation>
-<Title>Posttranslational modifications of human inter-alpha-inhibitor: identification of glycans and disulfide bridges in heavy chains 1 and 2.</Title>
-<Xref>DOI:10.1021/bi971137d</Xref>
-<Xref>PMID:9425062</Xref>
-<Note>mass spectrometric detection; the dihexosylation modification is not chemically characterized</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Oman, T.J.</Author>
-<Author>Boettcher, J.M.</Author>
-<Author>Wang, H.</Author>
-<Author>Okalibe, X.N.</Author>
-<Author>van der Donk, W.A.</Author>
-</Authors>
-<Citation>Nature Chem. Biol. 7, 78-80, 2011</Citation>
-<Title>Sublancin is not a lantibiotic but an S-linked glycopeptide.</Title>
-<Xref>DOI:10.1038/nchembio.509</Xref>
-<Xref>PMID:21196935</Xref>
-<Note>chromatographic, mass spectrometric, (1)H-NMR, and (13)C-NMR identification; chemical characterization; biosynthesis</Note>
-</ReferenceBlock>
-<Comment>The beta anomeric form is shown.</Comment>
-<Comment>See also RESID:AA0392 and RESID:AA0560 for other S-glycosylated cysteines.</Comment>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>GO:0018240</Xref>
-<Xref>PSI-MOD:00161</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__s-linked (glc) cysteine__c">CARBOHYD S-linked (Glc) cysteine</Feature>
-<Feature type="UniProt" key="carbohyd__s-linked (glc...) cysteine__c">CARBOHYD S-linked (Glc...) cysteine</Feature>
-<Feature type="UniProt" key="carbohyd__s-linked (hex...) cysteine__c">CARBOHYD S-linked (Hex...) cysteine</Feature>
-</Features>
-<Image src="/images/AA0152.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0152.PDB" />
-</Entry>
-<Entry id="AA0153">
-<Header>
-<Code>AA0153</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>30-Sep-2005</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O5-glucosylgalactosyl-L-hydroxylysine</Name>
-<AlternateName>5-(2-O-alpha-D-glucopyranosyl-beta-D-galactopyranosyl)oxy-L-lysine</AlternateName>
-<SystematicName>(2S,5R)-2,6-diamino-5-[2-O-(alpha-D-glucopyranosyl)-beta-D-galactopyranosyloxy]hexanoic acid</SystematicName>
-<Xref>CAS:32448-35-4</Xref>
-<Xref>ChEBI:138659</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 18 H 32 N 2 O 12</Formula>
-<Weight type="chemical">468.46</Weight>
-<Weight type="physical">468.195524</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 12 H 20 N 0 O 11</Formula>
-<Weight type="chemical">340.28</Weight>
-<Weight type="physical">340.100561</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Butler, W.T.</Author>
-<Author>Cunningham, L.W.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 241, 3882-3888, 1966</Citation>
-<Title>Evidence for the linkage of a disaccharide to hydroxylysine in tropocollagen.</Title>
-<Xref>PMID:4288358</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Morgan, P.H.</Author>
-<Author>Jacobs, H.G.</Author>
-<Author>Segrest, J.P.</Author>
-<Author>Cunningham, L.W.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 245, 5042-5048, 1970</Citation>
-<Title>Comparative study of glycopeptides derived from selected vertebrate collagens. A possible role of the carbohydrate in fibril formation.</Title>
-<Xref>PMID:4319110</Xref>
-<Note>attachment of 2-O-alpha-D-glucosyl-O-beta-D-galactose to 5-hydroxylysine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Allevi, P.</Author>
-<Author>Anastasia, M.</Author>
-<Author>Paroni, R.</Author>
-<Author>Ragusa, A.</Author>
-</Authors>
-<Citation>Bioorg. Med. Chem. Lett. 14, 3319-3321, 2004</Citation>
-<Title>The first synthesis of glucosylgalactosyl hydroxylysine (Glu-Gal-Hyl), an important biological indicator of collagen turnover.</Title>
-<Xref>DOI:10.1016/j.bmcl.2004.03.068</Xref>
-<Xref>PMID:15149698</Xref>
-<Note>chemical synthesis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Myllylä, R.</Author>
-<Author>Wang, C.</Author>
-<Author>Heikkinen, J.</Author>
-<Author>Juffer, A.</Author>
-<Author>Lampela, O.</Author>
-<Author>Risteli, M.</Author>
-<Author>Ruotsalainen, H.</Author>
-<Author>Salo, A.</Author>
-<Author>Sipilä, L.</Author>
-</Authors>
-<Citation>J. Cell. Physiol. 212, 323-329, 2007</Citation>
-<Title>Expanding the lysyl hydroxylase toolbox: new insights into the localization and activities of lysyl hydroxylase 3 (LH3).</Title>
-<Xref>DOI:10.1002/jcp.21036</Xref>
-<Xref>PMID:17516569</Xref>
-<Note>lysyl hydroxylase 3 (LH3) also possesses galactosyl transferase and glucosyl transferase activities</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Vitorino, R.</Author>
-<Author>Alves, R.</Author>
-<Author>Barros, A.</Author>
-<Author>Caseiro, A.</Author>
-<Author>Ferreira, R.</Author>
-<Author>Lobo, M.C.</Author>
-<Author>Bastos, A.</Author>
-<Author>Duarte, J.</Author>
-<Author>Carvalho, D.</Author>
-<Author>Santos, L.L.</Author>
-<Author>Amado, F.L.</Author>
-</Authors>
-<Citation>Proteomics 10, 3732-3742, 2010</Citation>
-<Title>Finding new posttranslational modifications in salivary proline-rich proteins.</Title>
-<Xref>DOI:10.1002/pmic.201000261</Xref>
-<Xref>PMID:20879038</Xref>
-<Note>mass spectrometric detection</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Perdivara, I.</Author>
-<Author>Perera, L.</Author>
-<Author>Sricholpech, M.</Author>
-<Author>Terajima, M.</Author>
-<Author>Pleshko, N.</Author>
-<Author>Yamauchi, M.</Author>
-<Author>Tomer, K.B.</Author>
-</Authors>
-<Citation>J. Am. Soc. Mass Spectrom. 24, 1072-1081, 2013</Citation>
-<Title>Unusual fragmentation pathways in collagen glycopeptides.</Title>
-<Xref>DOI:10.1007/s13361-013-0624-y</Xref>
-<Xref>PMID:23633013</Xref>
-<Note>mass spectrometric analysis of CID fragmentation patterns</Note>
-</ReferenceBlock>
-<Comment>Some forms of lysyl hydroxylase (EC 1.14.11.4) are multifunctional and possess both transferase activities.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>procollagen galactosyltransferase (EC 2.4.1.50)</EnzymeName>
-<EnzymeName>procollagen glucosyltransferase (EC 2.4.1.66)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Condition>secondary to RESID:AA0028</Condition>
-<Xref>GO:0006493</Xref>
-<Xref>GO:0018241</Xref>
-<Xref>PSI-MOD:00162</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__o-linked (gal...) hydroxylysine__k">CARBOHYD O-linked (Gal...) hydroxylysine</Feature>
-</Features>
-<Image src="/images/AA0153.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0153.PDB" />
-</Entry>
-<Entry id="AA0154">
-<Header>
-<Code>AA0154</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-2006</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-(N-acetylamino)galactosyl-L-serine</Name>
-<AlternateName>mucin type O-glycosylserine</AlternateName>
-<AlternateName>O3-(N-acetylgalactosaminyl)serine</AlternateName>
-<SystematicName>(2S)-2-amino-3-(2-acetamido-2-deoxy-alpha-D-galactopyranosyloxy)propanoic acid</SystematicName>
-<Xref>ChEBI:53604</Xref>
-<Xref>ChEBI:87078</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 11 H 18 N 2 O 7 +</Formula>
-<Weight type="chemical">290.27 +</Weight>
-<Weight type="physical">290.111401 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 8 H 13 N 1 O 5 +</Formula>
-<Weight type="chemical">203.19 +</Weight>
-<Weight type="physical">203.079373 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Robinson, E.A.</Author>
-<Author>Appella, E.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 254, 11418-11430, 1979</Citation>
-<Title>Amino acid sequence of a mouse myeloma immunoglobin heavy chain (MOPC 47 A) with a 100-residue deletion.</Title>
-<Xref>PMID:115869</Xref>
-<Note>O-glycosylation by N-acetylgalactosamine only</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wang, Y.</Author>
-<Author>Agrwal, N.</Author>
-<Author>Eckhardt, A.E.</Author>
-<Author>Stevens, R.D.</Author>
-<Author>Hill, R.L.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 268, 22979-22983, 1993</Citation>
-<Title>The acceptor substrate specificity of porcine submaxillary UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase is dependent on the amino acid sequences adjacent to serine and threonine residues.</Title>
-<Xref>PMID:8226812</Xref>
-<Note>N-acetylgalactosaminyltransferase transfers to either serine or threonine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hansen, J.E.</Author>
-<Author>Lund, O.</Author>
-<Author>Engelbrecht, J.</Author>
-<Author>Bohr, H.</Author>
-<Author>Nielsen, J.O.</Author>
-<Author>Hansen, J.E.S.</Author>
-<Author>Brunak, S.</Author>
-</Authors>
-<Citation>Biochem. J. 308, 801-813, 1995</Citation>
-<Title>Prediction of O-glycosylation of mammalian proteins: specificity patterns of UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase.</Title>
-<Xref>PMID:8948436</Xref>
-<Note>prediction using neural network; the omission of author "Brunak, S." in the PubMed citation is corrected</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gerken, T.A.</Author>
-<Author>Owens, C.L.</Author>
-<Author>Pasumarthy, M.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 272, 9709-9719, 1997</Citation>
-<Title>Determination of the site-specific O-glycosylation pattern of the porcine submaxillary mucin tandem repeat glycopeptide. Model proposed for the polypeptide:galnac transferase peptide binding site.</Title>
-<Xref>DOI:10.1074/jbc.272.15.9709</Xref>
-<Xref>PMID:9092502</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hang, H.C.</Author>
-<Author>Bertozzi, C.R.</Author>
-</Authors>
-<Citation>Bioorg. Med. Chem. 13, 5021-5034, 2005</Citation>
-<Title>The chemistry and biology of mucin-type O-linked glycosylation.</Title>
-<Xref>DOI:10.1016/j.bmc.2005.04.085</Xref>
-<Xref>PMID:16005634</Xref>
-</ReferenceBlock>
-<Comment>See also RESID:AA0208, RESID:AA0209, RESID:AA0210, RESID:AA0291, RESID:AA0296, RESID:AA0297, RESID:AA0397, RESID:AA0398, RESID:AA0400, RESID:AA0402, RESID:AA0404, RESID:AA0406, and RESID:AA0422 for other O-glycosylated serines.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>polypeptide N-acetylgalactosaminyltransferase (EC 2.4.1.41)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>GO:0006493</Xref>
-<Xref>GO:0018242</Xref>
-<Xref>PSI-MOD:00163</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__o-linked (galnac) serine__s">CARBOHYD O-linked (GalNAc) serine</Feature>
-<Feature type="UniProt" key="carbohyd__o-linked (galnac...) serine__s">CARBOHYD O-linked (GalNAc...) serine</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="carbohyd__o-linked (hexnac...) serine__s">CARBOHYD O-linked (HexNAc...) serine</Feature>
-<Note>this UniProt feature is used when the identity of the sugar has not been determined</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0154.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0154.PDB" />
-</Entry>
-<Entry id="AA0155">
-<Header>
-<Code>AA0155</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-2006</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-(N-acetylamino)galactosyl-L-threonine</Name>
-<AlternateName>mucin type O-glycosylthreonine</AlternateName>
-<AlternateName>O3-(N-acetylgalactosaminyl)threonine</AlternateName>
-<SystematicName>(2S,3R)-2-amino-3-(2-acetamido-2-deoxy-alpha-D-galactopyranosyloxy)butanoic acid</SystematicName>
-<Xref>ChEBI:87075</Xref>
-<Xref>PDBHET:GTH</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 12 H 20 N 2 O 7 +</Formula>
-<Weight type="chemical">304.30 +</Weight>
-<Weight type="physical">304.127051 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0017">
-<Formula>C 8 H 13 N 1 O 5 +</Formula>
-<Weight type="chemical">203.19 +</Weight>
-<Weight type="physical">203.079373 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Talbo, G.</Author>
-<Author>Højrup, P.</Author>
-<Author>Rahbek-Nielsen, H.</Author>
-<Author>Andersen, S.O.</Author>
-<Author>Roepstorff, P.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 195, 495-504, 1991</Citation>
-<Title>Determination of the covalent structure of an N- and C-terminally blocked glycoprotein from endocuticle of Locusta migratoria. Combined use of plasma desorption mass spectrometry and Edman degradation to study post-translationally modified proteins.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1991.tb15730.x</Xref>
-<Xref>PMID:1997327</Xref>
-<Note>O-glycosylation by N-acetylgalactosamine only</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wang, Y.</Author>
-<Author>Agrwal, N.</Author>
-<Author>Eckhardt, A.E.</Author>
-<Author>Stevens, R.D.</Author>
-<Author>Hill, R.L.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 268, 22979-22983, 1993</Citation>
-<Title>The acceptor substrate specificity of porcine submaxillary UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase is dependent on the amino acid sequences adjacent to serine and threonine residues.</Title>
-<Xref>PMID:8226812</Xref>
-<Note>N-acetylgalactosaminyltransferase transfers to either serine or threonine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hansen, J.E.</Author>
-<Author>Lund, O.</Author>
-<Author>Engelbrecht, J.</Author>
-<Author>Bohr, H.</Author>
-<Author>Nielsen, J.O.</Author>
-<Author>Hansen, J.E.S.</Author>
-<Author>Brunak, S.</Author>
-</Authors>
-<Citation>Biochem. J. 308, 801-813, 1995</Citation>
-<Title>Prediction of O-glycosylation of mammalian proteins: specificity patterns of UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase.</Title>
-<Xref>PMID:8948436</Xref>
-<Note>prediction using neural network; the omission of author "Brunak, S." in the PubMed citation is corrected</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gerken, T.A.</Author>
-<Author>Owens, C.L.</Author>
-<Author>Pasumarthy, M.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 272, 9709-9719, 1997</Citation>
-<Title>Determination of the site-specific O-glycosylation pattern of the porcine submaxillary mucin tandem repeat glycopeptide. Model proposed for the polypeptide:galnac transferase peptide binding site.</Title>
-<Xref>DOI:10.1074/jbc.272.15.9709</Xref>
-<Xref>PMID:9092502</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hang, H.C.</Author>
-<Author>Bertozzi, C.R.</Author>
-</Authors>
-<Citation>Bioorg. Med. Chem. 13, 5021-5034, 2005</Citation>
-<Title>The chemistry and biology of mucin-type O-linked glycosylation.</Title>
-<Xref>DOI:10.1016/j.bmc.2005.04.085</Xref>
-<Xref>PMID:16005634</Xref>
-</ReferenceBlock>
-<Comment>See also RESID:AA0247, RESID:AA0399, RESID:AA0401, RESID:AA0403, RESID:AA0405, and RESID:AA0515 for other O-glycosylated threonines.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>polypeptide N-acetylgalactosaminyltransferase (EC 2.4.1.41)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>T</SequenceSpec>
-<Xref>GO:0006493</Xref>
-<Xref>GO:0018243</Xref>
-<Xref>PSI-MOD:00164</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__o-linked (galnac) threonine__t">CARBOHYD O-linked (GalNAc) threonine</Feature>
-<Feature type="UniProt" key="carbohyd__o-linked (galnac...) threonine__t">CARBOHYD O-linked (GalNAc...) threonine</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="carbohyd__o-linked (hexnac) threonine__t">CARBOHYD O-linked (HexNAc) threonine</Feature>
-<Note>this UniProt feature is used when the identity of the sugar has not been determined</Note>
-</FeatureNote>
-<FeatureNote>
-<Feature type="UniProt" key="carbohyd__o-linked (hexnac...) threonine__t">CARBOHYD O-linked (HexNAc...) threonine</Feature>
-<Note>this UniProt feature is used when the identity of the sugar has not been determined</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0155.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0155.PDB" />
-</Entry>
-<Entry id="AA0156">
-<Header>
-<Code>AA0156</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-2006</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>1'-mannosyl-L-tryptophan</Name>
-<AlternateName>1'-glycosyl-L-tryptophan</AlternateName>
-<AlternateName>N-mannosyl-tryptophan</AlternateName>
-<AlternateName>N1-mannosyl-tryptophan</AlternateName>
-<SystematicName>(2S)-2-amino-3-(1-D-mannopyranosyloxy-1H-indol-3-yl)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 17 H 20 N 2 O 6</Formula>
-<Weight type="chemical">348.36</Weight>
-<Weight type="physical">348.132136</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0018">
-<Formula>C 6 H 10 N 0 O 5</Formula>
-<Weight type="chemical">162.14</Weight>
-<Weight type="physical">162.052823</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gäde, G.</Author>
-<Author>Kellner, R.</Author>
-<Author>Rinehart, K.L.</Author>
-<Author>Proefke, M.L.</Author>
-</Authors>
-<Citation>Biochem. Biophys. Res. Commun. 189, 1303-1309, 1992</Citation>
-<Title>A tryptophan-substituted member of the AKH/RPCH family isolated from a stick insect corpus cardiacum.</Title>
-<Xref>DOI:10.1016/0006-291X(92)90215-7</Xref>
-<Xref>PMID:1482345</Xref>
-<Note>proposed, without evidence, to be 1'- or N-linked</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gäde, G.</Author>
-</Authors>
-<Citation>Ann. N. Y. Acad. Sci. 839, 101-104, 1998</Citation>
-<Title>The adipokinetic hormone/red pigment-concentrating hormone family. New structure, unique post-translational modifications and a unique new physiological role.</Title>
-<Xref>DOI:10.1111/j.1749-6632.1998.tb10739.x</Xref>
-<Note>identified as a mannosyltryptophan, it was assumed to be 2'- or C-linked rather than 1'- or N-linked</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Schnabel, M.</Author>
-<Author>Römpp, B.</Author>
-<Author>Ruckdeschel, D.</Author>
-<Author>Unverzagt, C.</Author>
-</Authors>
-<Citation>Tetrahedron Lett. 45, 295-297, 2004</Citation>
-<Title>Synthesis of tryptophan N-glucoside.</Title>
-<Xref>DOI:10.1016/j.tetlet.2003.10.190</Xref>
-<Note>synthesis of 1'-glycosyltryptophan compounds</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Li, J.S.</Author>
-<Author>Cui, L.</Author>
-<Author>Rock, D.L.</Author>
-<Author>Li, J.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 280, 38513-38521, 2005</Citation>
-<Title>Novel glycosidic linkage in Aedes aegypti chorion peroxidase: N-mannosyl tryptophan.</Title>
-<Xref>DOI:10.1074/jbc.M508449200</Xref>
-<Xref>PMID:16150691</Xref>
-<Note>evidence that the 1'-mannosyltryptophan modification occurs in arthropods </Note>
-</ReferenceBlock>
-<Comment>In 1992, the hexose was not identified and it was proposed, but not established, that this modification had an N-linked glycosidic bond. After C-linked 2'-mannosyltryptophan was found in vertebrate proteins, it was generally assumed that the tryptophan N-glycoside structure was wrong. See RESID:AA0217 for 2'-mannosyltryptophan.</Comment>
-<Comment>The alpha anomeric form is shown.</Comment>
-<SequenceCode>
-<SequenceSpec>W</SequenceSpec>
-<Xref>GO:0006487</Xref>
-<Xref>GO:0018244</Xref>
-<Xref>PSI-MOD:00165</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__n-linked (man) tryptophan__w">CARBOHYD N-linked (Man) tryptophan</Feature>
-</Features>
-<Image src="/images/AA0156.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0156.PDB" />
-</Entry>
-<Entry id="AA0157">
-<Header>
-<Code>AA0157</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O4'-glucosyl-L-tyrosine</Name>
-<AlternateName>O4'-glycosyl-L-tyrosine</AlternateName>
-<SystematicName>(2S)-2-amino-3-(4-alpha-D-glucopyranosyloxy)phenylpropanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 15 H 19 N 1 O 7 +</Formula>
-<Weight type="chemical">325.32 +</Weight>
-<Weight type="physical">325.116152 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0019">
-<Formula>C 6 H 10 N 0 O 5 +</Formula>
-<Weight type="chemical">162.14 +</Weight>
-<Weight type="physical">162.052823 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Smythe, C.</Author>
-<Author>Caudwell, F.B.</Author>
-<Author>Ferguson, M.</Author>
-<Author>Cohen, P.</Author>
-</Authors>
-<Citation>EMBO J. 7, 2681-2686, 1988</Citation>
-<Title>Isolation and structural analysis of a peptide containing the novel tyrosyl-glucose linkage in glycogenin.</Title>
-<Xref>PMID:3181138</Xref>
-<Note>mass spectrometric and linkage analysis</Note>
-</ReferenceBlock>
-<Comment>The carbohydrate is glucose, the origin for glycogen. One to eleven alpha-1,4-linked glucose units may be auto-catalytically attached.</Comment>
-<Comment>See also RESID:AA0577 for other O-glycosylated tyrosines.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>glycogenin glucosyltransferase (EC 2.4.1.186)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>Y</SequenceSpec>
-<Xref>GO:0006493</Xref>
-<Xref>GO:0018245</Xref>
-<Xref>PSI-MOD:00166</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__o-linked (glc...) tyrosine__y">CARBOHYD O-linked (Glc...) tyrosine</Feature>
-</Features>
-<Image src="/images/AA0157.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0157.PDB" />
-</Entry>
-<Entry id="AA0158">
-<Header>
-<Code>AA0158</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Apr-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-asparaginyl-glycosylphosphatidylinositolethanolamine</Name>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 13 N 3 O 6 P 1 +</Formula>
-<Weight type="chemical">254.16 +</Weight>
-<Weight type="physical">254.054197 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0003">
-<Formula>C 2 H 6 N 1 O 3 P 1 +</Formula>
-<Weight type="chemical">123.05 +</Weight>
-<Weight type="physical">123.008530 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Nuoffer, C.</Author>
-<Author>Jenoe, P.</Author>
-<Author>Conzelmann, A.</Author>
-<Author>Riezman, H.</Author>
-</Authors>
-<Citation>Mol. Cell. Biol. 11, 27-37, 1991</Citation>
-<Title>Determinants for glycophospholipid anchoring of the Saccharomyces cerevisiae GAS1 protein to the plasma membrane.</Title>
-<Xref>PMID:1824714</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sugita, Y.</Author>
-<Author>Nakano, Y.</Author>
-<Author>Oda, E.</Author>
-<Author>Noda, K.</Author>
-<Author>Tobe, T.</Author>
-<Author>Miura, N.H.</Author>
-<Author>Tomita, M.</Author>
-</Authors>
-<Citation>J. Biochem. 114, 473-477, 1993</Citation>
-<Title>Determination of carboxyl-terminal residue and disulfide bonds of MACIF(CD59), a glycosyl-phosphatidylinositol-anchored membrane protein.</Title>
-<Xref>PMID:8276756</Xref>
-</ReferenceBlock>
-<Comment>A representative glycan core structure is shown.</Comment>
-<Comment>Cleavage of a carboxyl terminal propeptide accompanies transamidation.</Comment>
-<SequenceCode>
-<SequenceSpec>N</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0018265</Xref>
-<Xref>GO:0042050</Xref>
-<Xref>PSI-MOD:00167</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>glycoprotein</Keyword>
-<Keyword>lipoprotein</Keyword>
-<Keyword>phosphatidylinositol linkage</Keyword>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__gpi-anchor amidated asparagine__n">LIPID GPI-anchor amidated asparagine</Feature>
-</Features>
-<Image src="/images/AA0158.GIF" alt="DUMMY.GIF" />
-</Entry>
-<Entry id="AA0159">
-<Header>
-<Code>AA0159</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Apr-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-aspartyl-glycosylphosphatidylinositolethanolamine</Name>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 12 N 2 O 7 P 1 +</Formula>
-<Weight type="chemical">255.14 +</Weight>
-<Weight type="physical">255.038212 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0004">
-<Formula>C 2 H 6 N 1 O 3 P 1 +</Formula>
-<Weight type="chemical">123.05 +</Weight>
-<Weight type="physical">123.008530 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Allen, G.</Author>
-<Author>Gurnett, L.P.</Author>
-<Author>Cross, G.A.M.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 157, 527-546, 1982</Citation>
-<Title>Complete amino acid sequence of a variant surface glycoprotein (VSG 117) from Trypanosoma brucei.</Title>
-<Xref>DOI:10.1016/0022-2836(82)90474-0</Xref>
-<Xref>PMID:7120400</Xref>
-</ReferenceBlock>
-<Comment>A representative glycan core structure is shown.</Comment>
-<Comment>Cleavage of a carboxyl terminal propeptide accompanies transamidation.</Comment>
-<SequenceCode>
-<SequenceSpec>D</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0018266</Xref>
-<Xref>GO:0042050</Xref>
-<Xref>PSI-MOD:00168</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>glycoprotein</Keyword>
-<Keyword>lipoprotein</Keyword>
-<Keyword>phosphatidylinositol linkage</Keyword>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__gpi-anchor amidated aspartate__d">LIPID GPI-anchor amidated aspartate</Feature>
-</Features>
-<Image src="/images/AA0159.GIF" alt="DUMMY.GIF" />
-</Entry>
-<Entry id="AA0160">
-<Header>
-<Code>AA0160</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Apr-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-cysteinyl-glycosylphosphatidylinositolethanolamine</Name>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 12 N 2 O 5 P 1 S 1 +</Formula>
-<Weight type="chemical">243.19 +</Weight>
-<Weight type="physical">243.020454 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 2 H 6 N 1 O 3 P 1 S 0 +</Formula>
-<Weight type="chemical">123.05 +</Weight>
-<Weight type="physical">123.008530 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Homans, S.W.</Author>
-<Author>Ferguson, M.A.J.</Author>
-<Author>Dwek, R.A.</Author>
-<Author>Rademacher, T.W.</Author>
-<Author>Anand, R.</Author>
-<Author>Williams, A.F.</Author>
-</Authors>
-<Citation>Nature 333, 269-272, 1988</Citation>
-<Title>Complete structure of the glycosyl phosphatidylinositol membrane anchor of rat brain Thy-1 glycoprotein.</Title>
-<Xref>DOI:10.1038/333269a0</Xref>
-<Xref>PMID:2897081</Xref>
-</ReferenceBlock>
-<Comment>A representative glycan core structure is shown.</Comment>
-<Comment>Cleavage of a carboxyl terminal propeptide accompanies transamidation.</Comment>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0018267</Xref>
-<Xref>GO:0042050</Xref>
-<Xref>PSI-MOD:00169</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>glycoprotein</Keyword>
-<Keyword>lipoprotein</Keyword>
-<Keyword>phosphatidylinositol linkage</Keyword>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__gpi-anchor amidated cysteine__c">LIPID GPI-anchor amidated cysteine</Feature>
-</Features>
-<Image src="/images/AA0160.GIF" alt="DUMMY.GIF" />
-</Entry>
-<Entry id="AA0161">
-<Header>
-<Code>AA0161</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Apr-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-glycyl-glycosylphosphatidylinositolethanolamine</Name>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 10 N 2 O 5 P 1 +</Formula>
-<Weight type="chemical">197.11 +</Weight>
-<Weight type="physical">197.032733 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0008">
-<Formula>C 2 H 6 N 1 O 3 P 1 +</Formula>
-<Weight type="chemical">123.05 +</Weight>
-<Weight type="physical">123.008530 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hefta, S.A.</Author>
-<Author>Paxton, R.J.</Author>
-<Author>Shively, J.E.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 265, 8618-8626, 1990</Citation>
-<Title>Sequence and glycosylation site identity of two distinct glycoforms of nonspecific cross-reacting antigen as demonstrated by sequence analysis and fast atom bombardment mass spectrometry.</Title>
-<Xref>PMID:2341397</Xref>
-</ReferenceBlock>
-<Comment>A representative glycan core structure is shown.</Comment>
-<Comment>Cleavage of a carboxyl terminal propeptide accompanies transamidation.</Comment>
-<SequenceCode>
-<SequenceSpec>G</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0018268</Xref>
-<Xref>GO:0042050</Xref>
-<Xref>PSI-MOD:00170</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>glycoprotein</Keyword>
-<Keyword>lipoprotein</Keyword>
-<Keyword>phosphatidylinositol linkage</Keyword>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__gpi-anchor amidated glycine__g">LIPID GPI-anchor amidated glycine</Feature>
-</Features>
-<Image src="/images/AA0161.GIF" alt="DUMMY.GIF" />
-</Entry>
-<Entry id="AA0162">
-<Header>
-<Code>AA0162</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Apr-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-seryl-glycosylphosphatidylinositolethanolamine</Name>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 12 N 2 O 6 P 1 +</Formula>
-<Weight type="chemical">227.13 +</Weight>
-<Weight type="physical">227.043298 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 2 H 6 N 1 O 3 P 1 +</Formula>
-<Weight type="chemical">123.05 +</Weight>
-<Weight type="physical">123.008530 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Zhu, X.L.</Author>
-<Author>Sly, W.S.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 265, 8795-8801, 1990</Citation>
-<Title>Carbonic anhydrase IV from human lung. Purification, characterization, and comparison with membrane carbonic anhydrase from human kidney.</Title>
-<Xref>PMID:2111324</Xref>
-<Note>evidence for glycosyl phosphatidylinositol anchor</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Stahl, N.</Author>
-<Author>Baldwin, M.A.</Author>
-<Author>Teplow, D.B.</Author>
-<Author>Hood, L.</Author>
-<Author>Gibson, B.W.</Author>
-<Author>Burlingame, A.L.</Author>
-<Author>Prusiner, S.B.</Author>
-</Authors>
-<Citation>Biochemistry 32, 1991-2002, 1993</Citation>
-<Title>Structural studies of the scrapie prion protein using mass spectrometry and amino acid sequencing.</Title>
-<Xref>DOI:10.1021/bi00059a016</Xref>
-<Xref>PMID:8448158</Xref>
-<Note>mass spectrometric and chemical characterization</Note>
-</ReferenceBlock>
-<Comment>A representative glycan core structure is shown.</Comment>
-<Comment>Cleavage of a carboxyl terminal propeptide accompanies transamidation.</Comment>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0018269</Xref>
-<Xref>GO:0042050</Xref>
-<Xref>PSI-MOD:00171</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>glycoprotein</Keyword>
-<Keyword>lipoprotein</Keyword>
-<Keyword>phosphatidylinositol linkage</Keyword>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__gpi-anchor amidated serine__s">LIPID GPI-anchor amidated serine</Feature>
-</Features>
-<Image src="/images/AA0162.GIF" alt="DUMMY.GIF" />
-</Entry>
-<Entry id="AA0163">
-<Header>
-<Code>AA0163</Code>
-<Dates>
-<CreationDate>28-Jan-2000</CreationDate>
-<StrucRevDate>28-Jan-2000</StrucRevDate>
-<TextChngDate>30-Apr-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-alanyl-glycosylphosphatidylinositolethanolamine</Name>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 12 N 2 O 5 P 1 +</Formula>
-<Weight type="chemical">211.13 +</Weight>
-<Weight type="physical">211.048383 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0001">
-<Formula>C 2 H 6 N 1 O 3 P 1 +</Formula>
-<Weight type="chemical">123.05 +</Weight>
-<Weight type="physical">123.008530 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Moy, P.</Author>
-<Author>Lobb, R.</Author>
-<Author>Tizard, R.</Author>
-<Author>Olson, D.</Author>
-<Author>Hession, C.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 268, 8835-8841, 1993</Citation>
-<Title>Cloning of an inflammation-specific phosphatidyl inositol-linked form of murine vascular cell adhesion molecule-1.</Title>
-<Xref>PMID:7682556</Xref>
-<Note>predicted cleavage site</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Vergas Romero, C.</Author>
-<Author>Neudorfer, I.</Author>
-<Author>Mann, K.</Author>
-<Author>Schäfer, D.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 229, 262-269, 1995</Citation>
-<Title>Purification and amino acid sequence of aminopeptidase P from pig kidney.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1995.0262l.x</Xref>
-<Xref>PMID:7744038</Xref>
-<Note>enzymatic and sequence evidence</Note>
-</ReferenceBlock>
-<Comment>A representative glycan core structure is shown.</Comment>
-<Comment>Cleavage of a carboxyl terminal propeptide accompanies transamidation.</Comment>
-<SequenceCode>
-<SequenceSpec>A</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0018270</Xref>
-<Xref>GO:0042050</Xref>
-<Xref>PSI-MOD:00172</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>glycoprotein</Keyword>
-<Keyword>lipoprotein</Keyword>
-<Keyword>phosphatidylinositol linkage</Keyword>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__gpi-anchor amidated alanine__a">LIPID GPI-anchor amidated alanine</Feature>
-</Features>
-<Image src="/images/AA0163.GIF" alt="DUMMY.GIF" />
-</Entry>
-<Entry id="AA0164">
-<Header>
-<Code>AA0164</Code>
-<Dates>
-<CreationDate>30-Sep-2003</CreationDate>
-<StrucRevDate>30-Sep-2003</StrucRevDate>
-<TextChngDate>30-Apr-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-threonyl-glycosylphosphatidylinositolethanolamine</Name>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 14 N 2 O 6 P 1 +</Formula>
-<Weight type="chemical">241.16 +</Weight>
-<Weight type="physical">241.058948 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0017">
-<Formula>C 2 H 6 N 1 O 3 P 1 +</Formula>
-<Weight type="chemical">123.05 +</Weight>
-<Weight type="physical">123.008530 +</Weight>
-</CorrectionBlock>
-<Comment>This modification is predicted for proteins with sequence characteristics for the GPI-anchor modification, and with threonine at the cleavage and anchor attachment site.</Comment>
-<Comment>A representative glycan core structure is shown.</Comment>
-<Comment>Cleavage of a carboxyl terminal propeptide accompanies transamidation.</Comment>
-<SequenceCode>
-<SequenceSpec>T</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0050493</Xref>
-<Xref>PSI-MOD:00173</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>glycoprotein</Keyword>
-<Keyword>lipoprotein</Keyword>
-<Keyword>phosphatidylinositol linkage</Keyword>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__gpi-anchor amidated threonine__t">LIPID GPI-anchor amidated threonine</Feature>
-</Features>
-<Image src="/images/AA0164.GIF" alt="DUMMY.GIF" />
-</Entry>
-<Entry id="AA0165">
-<Header>
-<Code>AA0165</Code>
-<Dates>
-<CreationDate>30-Sep-2003</CreationDate>
-<StrucRevDate>30-Sep-2003</StrucRevDate>
-<TextChngDate>30-Apr-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-glycyl-glycosylsphingolipidinositolethanolamine</Name>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 10 N 2 O 5 P 1 +</Formula>
-<Weight type="chemical">197.11 +</Weight>
-<Weight type="physical">197.032733 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0008">
-<Formula>C 2 H 6 N 1 O 3 P 1 +</Formula>
-<Weight type="chemical">123.05 +</Weight>
-<Weight type="physical">123.008530 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Haynes, P.A.</Author>
-<Author>Gooley, A.A.</Author>
-<Author>Ferguson, M.A.</Author>
-<Author>Redmond, J.W.</Author>
-<Author>Williams, K.L.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 216, 729-737, 1993</Citation>
-<Title>Post-translational modifications of the Dictyostelium discoideum glycoprotein PsA. Glycosylphosphatidylinositol membrane anchor and composition of O-linked oligosaccharides.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1993.tb18192.x</Xref>
-<Xref>PMID:8404891</Xref>
-<Note>despite identifying the lipid as monoacylated phosphoceramide inositol, which does not contain glycerol, the authors repeatedly refer to it incorrectly as a phosphatidyl inositol, which would contain glycerol</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fontaine, T.</Author>
-<Author>Magnin, T.</Author>
-<Author>Melhert, A.</Author>
-<Author>Lamont, D.</Author>
-<Author>Latge, J.P.</Author>
-<Author>Ferguson, M.A.</Author>
-</Authors>
-<Citation>Glycobiology 13, 169-177, 2003</Citation>
-<Title>Structures of the glycosylphosphatidylinositol membrane anchors from Aspergillus fumigatus membrane proteins.</Title>
-<Xref>DOI:10.1093/glycob/cwg004</Xref>
-<Xref>PMID:12626404</Xref>
-</ReferenceBlock>
-<Comment>A representative glycan core structure is shown.</Comment>
-<Comment>Cleavage of a carboxyl terminal propeptide accompanies transamidation.</Comment>
-<SequenceCode>
-<SequenceSpec>G</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0050494</Xref>
-<Xref>PSI-MOD:00174</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>glycoprotein</Keyword>
-<Keyword>lipoprotein</Keyword>
-<Keyword>phosphoprotein</Keyword>
-<Keyword>sphingolipidinositol linkage</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__gpi-like-anchor amidated glycine__g">LIPID GPI-like-anchor amidated glycine</Feature>
-</Features>
-<Image src="/images/AA0165.GIF" alt="DUMMY.GIF" />
-</Entry>
-<Entry id="AA0166">
-<Header>
-<Code>AA0166</Code>
-<Dates>
-<CreationDate>09-Aug-1995</CreationDate>
-<StrucRevDate>09-Aug-1995</StrucRevDate>
-<TextChngDate>30-Apr-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-seryl-glycosylsphingolipidinositolethanolamine</Name>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 12 N 2 O 6 P 1 +</Formula>
-<Weight type="chemical">227.13 +</Weight>
-<Weight type="physical">227.043298 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 2 H 6 N 1 O 3 P 1 +</Formula>
-<Weight type="chemical">123.05 +</Weight>
-<Weight type="physical">123.008530 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Stadler, J.</Author>
-<Author>Keenan, T.W.</Author>
-<Author>Bauer, G.</Author>
-<Author>Gerisch, G.</Author>
-</Authors>
-<Citation>EMBO J. 8, 371-377, 1989</Citation>
-<Title>The contact site A glycoprotein of Dictyostelium discoideum carries a phospholipid anchor of a novel type.</Title>
-<Xref>PMID:2721485</Xref>
-<Note>partial chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Saito, T.</Author>
-<Author>Ochiai, H.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 218, 623-628, 1993</Citation>
-<Title>Evidence for a glycolipid anchor of gp64, a putative cell-cell adhesion protein of Polysphondylium pallidum.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1993.tb18415.x</Xref>
-<Xref>PMID:8269952</Xref>
-<Note>mass spectrometric and chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fontaine, T.</Author>
-<Author>Magnin, T.</Author>
-<Author>Melhert, A.</Author>
-<Author>Lamont, D.</Author>
-<Author>Latge, J.P.</Author>
-<Author>Ferguson, M.A.</Author>
-</Authors>
-<Citation>Glycobiology 13, 169-177, 2003</Citation>
-<Title>Structures of the glycosylphosphatidylinositol membrane anchors from Aspergillus fumigatus membrane proteins.</Title>
-<Xref>DOI:10.1093/glycob/cwg004</Xref>
-<Xref>PMID:12626404</Xref>
-</ReferenceBlock>
-<Comment>A representative glycan core structure is shown.</Comment>
-<Comment>Cleavage of a carboxyl terminal propeptide accompanies transamidation.</Comment>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0018281</Xref>
-<Xref>GO:0042050</Xref>
-<Xref>PSI-MOD:00175</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>glycoprotein</Keyword>
-<Keyword>lipoprotein</Keyword>
-<Keyword>phosphoprotein</Keyword>
-<Keyword>sphingolipidinositol linkage</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__gpi-like-anchor amidated serine__s">LIPID GPI-like-anchor amidated serine</Feature>
-</Features>
-<Image src="/images/AA0166.GIF" alt="DUMMY.GIF" />
-</Entry>
-<Entry id="AA0167">
-<Header>
-<Code>AA0167</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Sep-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-(phosphoribosyl dephospho-coenzyme A)-L-serine</Name>
-<AlternateName>O3-(phosphate-5-ribosyl-alpha-2-adenosine-5-diphosphate pantetheine)-L-serine</AlternateName>
-<AlternateName>O3-(phosphoribosyl dephospho-coenzyme A)-L-serine</AlternateName>
-<AlternateName>O3-2'-(5''-phosphoribosyl-3'-dephosphocoenzyme A)-L-serine</AlternateName>
-</Names>
-<FormulaBlock>
-<Formula>C 29 H 47 N 8 O 21 P 3 S 1</Formula>
-<Weight type="chemical">968.71</Weight>
-<Weight type="physical">968.178931</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 26 H 42 N 7 O 19 P 3 S 1</Formula>
-<Weight type="chemical">881.63</Weight>
-<Weight type="physical">881.146903</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Dimroth, P.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 64, 269-281, 1976</Citation>
-<Title>The prosthetic group of citrate-lyase acyl-carrier protein.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1976.00269.pp.x</Xref>
-<Xref>PMID:179809</Xref>
-<Note>chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Robinson Jr., J.B.</Author>
-<Author>Singh, M.</Author>
-<Author>Srere, P.A.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 73, 1872-1876, 1976</Citation>
-<Title>Structure of the prosthetic group of Klebsiella aerogenes citrate (pro-3S)-lyase.</Title>
-<Xref>DOI:10.1073/pnas.73.6.1872</Xref>
-<Xref>PMID:180526</Xref>
-<Note>chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Oppenheimer, N.J.</Author>
-<Author>Singh, M.</Author>
-<Author>Sweeley, C.C.</Author>
-<Author>Sung, S.J.</Author>
-<Author>Srere, P.A.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 254, 1000-1002, 1979</Citation>
-<Title>The configuration and location of the ribosidic linkage in the prosthetic group of citrate lyase (Klebsiella aerogenes).</Title>
-<Xref>PMID:368065</Xref>
-<Note>NMR and mass spectrometry of permethylation derivatives establish that phosphoribosyl glycosidic linkage is alpha 1-&gt;2</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Schneider, K.</Author>
-<Author>Dimroth, P.</Author>
-<Author>Bott, M.</Author>
-</Authors>
-<Citation>Biochemistry 39, 9438-9450, 2000</Citation>
-<Title>Biosynthesis of the prosthetic group of citrate lyase.</Title>
-<Xref>DOI:10.1021/bi000401r</Xref>
-<Xref>PMID:10924139</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hoenke, S.</Author>
-<Author>Wild, M.R.</Author>
-<Author>Dimroth, P.</Author>
-</Authors>
-<Citation>Biochemistry 39, 13223-13232, 2000</Citation>
-<Title>Biosynthesis of triphosphoribosyl-dephospho-coenzyme A, the precursor of the prosthetic group of malonate decarboxylase.</Title>
-<Xref>DOI:10.1021/bi0011532</Xref>
-<Xref>PMID:11052675</Xref>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>holo-ACP synthase (EC 2.7.7.61)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>GO:0018247</Xref>
-<Xref>PSI-MOD:00176</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>coenzyme A</Keyword>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__o-(phosphoribosyl dephospho-coenzyme a)serine__s">MOD_RES O-(phosphoribosyl dephospho-coenzyme A)serine</Feature>
-</Features>
-<Image src="/images/AA0167.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0167.PDB" />
-</Entry>
-<Entry id="AA0168">
-<Header>
-<Code>AA0168</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N(omega)-(ADP-ribosyl)-L-arginine</Name>
-<AlternateName>N(omega)-alpha-D-ribofuranosyl-L-arginine 5'-&gt;5'-ester with adenosine 5'-(trihydrogen diphosphate)</AlternateName>
-<AlternateName>N(omega)-[alpha-D-ribofuranoside 5'-&gt;5'-ester with adenosine 5'-(trihydrogen diphosphate)]-L-arginine</AlternateName>
-<SystematicName>(S)-2-amino-5-([imino([adenosine 5'-(trihydrogen diphosphate) 5'-&gt;5'-ester with alpha-D-ribofuranosyl]amino)methyl]amino)pentanoic acid</SystematicName>
-<Xref>CAS:71388-78-8</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 21 H 33 N 9 O 14 P 2</Formula>
-<Weight type="chemical">697.49</Weight>
-<Weight type="physical">697.162220</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0002">
-<Formula>C 15 H 21 N 5 O 13 P 2</Formula>
-<Weight type="chemical">541.30</Weight>
-<Weight type="physical">541.061109</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Oppenheimer, N.J.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 253, 4907-4910, 1978</Citation>
-<Title>Structural determination and stereospecificity of the choleragen-catalyzed reaction of NAD+ with guanidines.</Title>
-<Xref>PMID:209022</Xref>
-<Note>mass spectrometric and (1)H-NMR characterization; chemical synthesis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Van Dop, C.</Author>
-<Author>Tsubokawa, M.</Author>
-<Author>Bourne, H.R.</Author>
-<Author>Ramachandran, J.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 259, 696-698, 1984</Citation>
-<Title>Amino acid sequence of retinal transducin at the site ADP-ribosylated by cholera toxin.</Title>
-<Xref>PMID:6582062</Xref>
-<Note>mass spectrometric analysis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Pope, M.R.</Author>
-<Author>Murrell, S.A.</Author>
-<Author>Ludden, P.W.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 82, 3173-3177, 1985</Citation>
-<Title>Covalent modification of the iron protein of nitrogenase from Rhodospirillum rubrum by adenosine diphosphoribosylation of a specific arginine residue.</Title>
-<Xref>DOI:10.1073/pnas.82.10.3173</Xref>
-<Xref>PMID:3923473</Xref>
-<Note>mass spectrometric, (1)H-NMR and (31)P-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Pope, M.R.</Author>
-<Author>Saari, L.L.</Author>
-<Author>Ludden, P.W.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 261, 10104-10111, 1986</Citation>
-<Title>N-glycohydrolysis of adenosine diphosphoribosyl arginine linkages by dinitrogenase reductase activating glycohydrolase (activating enzyme) from Rhodospirillum rubrum.</Title>
-<Xref>PMID:3090031</Xref>
-<Note>stereochemical characterization; ADP-ribosyl-nitrogenase hydrolase (EC 3.2.2.24) appears to remove only the alpha anomeric form</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Osago, H.</Author>
-<Author>Yamada, K.</Author>
-<Author>Shibata, T.</Author>
-<Author>Yoshino, K.-I.</Author>
-<Author>Hara, N.</Author>
-<Author>Tsuchiya, M.</Author>
-</Authors>
-<Citation>Anal. Biochem. 393, 248-254, 2009</Citation>
-<Title>Precursor ion scanning and sequencing of arginine-ADP-ribosylated peptide by mass spectrometry.</Title>
-<Xref>DOI:10.1016/j.ab.2009.06.028</Xref>
-<Xref>PMID:19560435</Xref>
-<Note>detection of N-(ADP-ribosyl)-carbodiimide as a marker ion for ADP-ribosylation in MS/MS analysis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Matic, I.</Author>
-<Author>Ahel, I.</Author>
-<Author>Hay, R.T.</Author>
-</Authors>
-<Citation>Nature Methods 9, 771-772, 2012</Citation>
-<Title>Reanalysis of phosphoproteomics data uncovers ADP-ribosylation sites.</Title>
-<Xref>DOI:10.1038/nmeth.2106</Xref>
-<Xref>PMID:22847107</Xref>
-<Note>mass spectrometric detection in reanalysis of phosphoproteomics data</Note>
-</ReferenceBlock>
-<Comment>Cholera toxin appears to catalyze formation of the alpha form which subsequently anomerizes to approximately equal concentrations of the alpha and beta forms. The alpha form is presented.</Comment>
-<Comment>The keyword "phosphoprotein" is not used with toxin modification.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>NAD(P)+--arginine ADP-ribosyltransferase (EC 2.4.2.31)</EnzymeName>
-<EnzymeName>NAD+--nitrogenase ADP-D-ribosyltransferase (EC 2.4.2.37)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>R</SequenceSpec>
-<Xref>GO:0006471</Xref>
-<Xref>GO:0018120</Xref>
-<Xref>PSI-MOD:00177</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>*phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__adp-ribosylarginine__r">MOD_RES ADP-ribosylarginine</Feature>
-</Features>
-<Image src="/images/AA0168.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0168.PDB" />
-</Entry>
-<Entry id="AA0169">
-<Header>
-<Code>AA0169</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Sep-2008</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-(ADP-ribosyl)-L-cysteine</Name>
-<AlternateName>S-alpha-D-ribofuranosyl-L-cysteine 5'-&gt;5'-ester with adenosine 5'-(trihydrogen diphosphate)</AlternateName>
-<AlternateName>S-L-cysteine alpha-D-ribofuranoside 5'-&gt;5'-ester with adenosine 5'-(trihydrogen diphosphate)</AlternateName>
-<SystematicName>(R)-2-amino-3-([adenosine 5'-(trihydrogen diphosphate) 5'-&gt;5'-ester with alpha-D-ribofuranosyl]sulfanyl)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 18 H 26 N 6 O 14 P 2 S 1</Formula>
-<Weight type="chemical">644.44</Weight>
-<Weight type="physical">644.070294</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 15 H 21 N 5 O 13 P 2 S 0</Formula>
-<Weight type="chemical">541.30</Weight>
-<Weight type="physical">541.061109</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>West Jr., R.E.</Author>
-<Author>Moss, J.</Author>
-<Author>Vaughan, M.</Author>
-<Author>Liu, T.</Author>
-<Author>Liu, T.Y.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 260, 14428-14430, 1985</Citation>
-<Title>Pertussis toxin-catalyzed ADP-ribosylation of transducin. Cysteine 347 is the ADP-ribose acceptor site.</Title>
-<Xref>PMID:3863818</Xref>
-<Note>radioisotope labeling; chromatographic separation</Note>
-</ReferenceBlock>
-<Comment>The anomeric form of the pertussis toxin product has not been characterized; the alpha form is presented.</Comment>
-<Comment>The keywords "phosphoprotein" and "thioether bond" are not used with toxin modification.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>NAD(P)+--cysteine ADP-ribosyltransferase (EC 2.4.2.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>GO:0006471</Xref>
-<Xref>GO:0018123</Xref>
-<Xref>PSI-MOD:00178</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>*phosphoprotein</Keyword>
-<Keyword>*thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__adp-ribosylcysteine__c">MOD_RES ADP-ribosylcysteine</Feature>
-</Features>
-<Image src="/images/AA0169.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0169.PDB" />
-</Entry>
-<Entry id="AA0170">
-<Header>
-<Code>AA0170</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>20-Nov-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>5-L-glutamyl glycerylphosphorylethanolamine</Name>
-<AlternateName>L-glutamyl 5-glycerophosphoethanolamine</AlternateName>
-<AlternateName>L-glutamyl 5-glycerophosphorylethanolamine</AlternateName>
-<AlternateName>L-glutamyl 5-glycerylphosphorylethanolamine</AlternateName>
-<SystematicName>(S)-2-amino-5-[2-([([2,3-dihydroxypropyl]oxy)(hydroxy)phosphoryl]oxy)ethyl]amino-5-oxopentanoic acid</SystematicName>
-<Xref>CAS:1190-00-7</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 10 H 19 N 2 O 8 P 1</Formula>
-<Weight type="chemical">326.24</Weight>
-<Weight type="physical">326.087902</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0006">
-<Formula>C 5 H 12 N 1 O 5 P 1</Formula>
-<Weight type="chemical">197.13</Weight>
-<Weight type="physical">197.045309</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Dever, T.E.</Author>
-<Author>Costello, C.E.</Author>
-<Author>Owens, C.L.</Author>
-<Author>Rosenberry, T.L.</Author>
-<Author>Merrick, W.C.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 264, 20518-20525, 1989</Citation>
-<Title>Location of seven post-translational modifications in rabbit elongation factor 1alpha including dimethyllysine, trimethyllysine, and glycerylphosphorylethanolamine.</Title>
-<Xref>PMID:2511205</Xref>
-<Note>mass spectrometric and chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Whiteheart, S.W.</Author>
-<Author>Shenbagamurthi, P.</Author>
-<Author>Chen, L.</Author>
-<Author>Cotter, R.J.</Author>
-<Author>Hart, G.W.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 264, 14334-14341, 1989</Citation>
-<Title>Murine elongation factor 1alpha (EF-1alpha) is posttranslationally modified by novel amide-linked ethanolamine-phosphoglycerol moieties. Addition of ethanolamine-phosphoglycerol to specific glutamic acid residues on EF-1alpha.</Title>
-<Xref>PMID:2569467</Xref>
-<Note>mass spectrometric and chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ransom, W.D.</Author>
-<Author>Lao, P.-C.</Author>
-<Author>Gage, D.A.</Author>
-<Author>Boss, W.F.</Author>
-</Authors>
-<Citation>Plant Physiol. 117, 949-960, 1998</Citation>
-<Title>Phosphoglycerylethanolamine posttranslational modification of plant eukaryotic elongation factor 1alpha.</Title>
-<Xref>DOI:10.1104/pp.117.3.949</Xref>
-<Xref>PMID:9662537</Xref>
-<Note>mass spectrometric detection; isotope labeling; possible secondary modification by long chain fatty acylation; the punctuation of "Lao, P.C." in the PubMed citation is corrected</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Signorell, A.</Author>
-<Author>Jelk, J.</Author>
-<Author>Rauch, M.</Author>
-<Author>Bütikofer, P.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 283, 20320-20329, 2008</Citation>
-<Title>Phosphatidylethanolamine is the precursor of the ethanolamine phosphoglycerol moiety bound to eukaryotic elongation factor 1A.</Title>
-<Xref>DOI:10.1074/jbc.M802430200</Xref>
-<Xref>PMID:18499667</Xref>
-<Note>mass spectrometric detection and linkage analysis</Note>
-</ReferenceBlock>
-<Comment>5-Glutamyl glycerylphosphorylethanolamine appears to occur uniquely in translation elongation factor eEF-1 alpha chains. It is known to be a modification of glutamic acid. The stereochemistry of the glycerol phosphate has not been determined. The sn-3 form is shown.</Comment>
-<Comment>It has been established that is possible for the glycerol group to be secondarily modified by conjugation with long chain fatty acids, but probably not with inositol-containing lipids or glycolipids. The predominant soluble form is not lipidated, and the modified protein does not appear to be membrane associated.</Comment>
-<SequenceCode>
-<SequenceSpec>E</SequenceSpec>
-<Xref>GO:0018072</Xref>
-<Xref>PSI-MOD:00179</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__5-glutamyl glycerylphosphorylethanolamine__e">MOD_RES 5-glutamyl glycerylphosphorylethanolamine</Feature>
-</Features>
-<Image src="/images/AA0170.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0170.PDB" />
-</Entry>
-<Entry id="AA0171">
-<Header>
-<Code>AA0171</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-Dec-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-sulfo-L-cysteine</Name>
-<AlternateName>2-amino-3-(sulfothio)propanoic acid</AlternateName>
-<AlternateName>3-(sulfosulfanyl)-L-alanine</AlternateName>
-<AlternateName>cysteine sulfate thioester</AlternateName>
-<AlternateName>cysteine-S-sulfonic acid</AlternateName>
-<AlternateName>S-sulfocysteine</AlternateName>
-<SystematicName>(2R)-2-amino-3-(sulfosulfanyl)propanoic acid</SystematicName>
-<Xref>CAS:1637-71-4</Xref>
-<Xref>ChEBI:27891</Xref>
-<Xref>PDBHET:CSU</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 5 N 1 O 4 S 2</Formula>
-<Weight type="chemical">183.20</Weight>
-<Weight type="physical">182.966000</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 0 H 0 N 0 O 3 S 1</Formula>
-<Weight type="chemical">80.06</Weight>
-<Weight type="physical">79.956815</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ploegman, J.H.</Author>
-<Author>Drent, G.</Author>
-<Author>Kalk, K.H.</Author>
-<Author>Hol, W.G.J.</Author>
-<Author>Heinrikson, R.L.</Author>
-<Author>Keim, P.</Author>
-<Author>Weng, L.</Author>
-<Author>Russell, J.</Author>
-</Authors>
-<Citation>Nature 273, 124-129, 1978</Citation>
-<Title>The covalent and tertiary structure of bovine liver rhodanese.</Title>
-<Xref>DOI:10.1038/273124a0</Xref>
-<Xref>PMID:643076</Xref>
-<Note>X-ray diffraction, 2.9 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lim, A.</Author>
-<Author>Prokaeva, T.</Author>
-<Author>McComb, M.E.</Author>
-<Author>Connors, L.H.</Author>
-<Author>Skinner, M.</Author>
-<Author>Costello, C.E.</Author>
-</Authors>
-<Citation>Protein Sci. 12, 1775-1785, 2003</Citation>
-<Title>Identification of S-sulfonation and S-thiolation of a novel transthyretin Phe33Cys variant from a patient diagnosed with familial transthyretin amyloidosis.</Title>
-<Xref>DOI:10.1110/ps.0349703</Xref>
-<Xref>PMID:12876326</Xref>
-<Note>mass spectrometric detection of S-sulfocysteine in a mutant protein</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gales, L.</Author>
-<Author>Saraiva, M.J.</Author>
-<Author>Damas, A.M.</Author>
-</Authors>
-<Citation>Biochim. Biophys. Acta 1774, 59-64, 2007</Citation>
-<Title>Structural basis for the protective role of sulfite against transthyretin amyloid formation.</Title>
-<Xref>DOI:10.1016/j.bbapap.2006.10.015</Xref>
-<Xref>PMID:17175208</Xref>
-<Note>X-ray diffraction, 1.45 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gales, L.</Author>
-<Author>Damas, A.M.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, May 2006</Citation>
-<Description>Crystal structure of Cys10 sulfonated transthyretin.</Description>
-<Xref>PDB:2H4E</Xref>
-<Note>X-ray diffraction, 1.45 angstroms</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>GO:0018248</Xref>
-<Xref>PSI-MOD:00180</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>sulfoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="act_site____c">ACT_SITE</Feature>
-</Features>
-<Image src="/images/AA0171.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0171.PDB" />
-</Entry>
-<Entry id="AA0172">
-<Header>
-<Code>AA0172</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O4'-sulfo-L-tyrosine</Name>
-<AlternateName>2-amino-3-(4-hydroxyphenyl)propanoic acid 4'-sulfate</AlternateName>
-<AlternateName>O4-sulfotyrosine</AlternateName>
-<AlternateName>tyrosine sulfate</AlternateName>
-<AlternateName>tyrosine-O-sulfonic acid</AlternateName>
-<AlternateName>tyrosine-O-sulphonic acid</AlternateName>
-<SystematicName>(S)-2-amino-3-(4-sulfooxyphenyl)propanoic acid</SystematicName>
-<Xref>CAS:956-46-7</Xref>
-<Xref>ChEBI:65316</Xref>
-<Xref>PDBHET:TYS</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 9 N 1 O 5 S 1</Formula>
-<Weight type="chemical">243.23</Weight>
-<Weight type="physical">243.020143</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0019">
-<Formula>C 0 H 0 N 0 O 3 S 1</Formula>
-<Weight type="chemical">80.06</Weight>
-<Weight type="physical">79.956815</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Nachman, R.J.</Author>
-<Author>Holman, G.M.</Author>
-<Author>Cook, B.J.</Author>
-<Author>Haddon, W.F.</Author>
-<Author>Ling, N.</Author>
-</Authors>
-<Citation>Biochem. Biophys. Res. Commun. 140, 357-364, 1986</Citation>
-<Title>Leucosulfakinin-II, a blocked sulfated insect neuropeptide with homology to cholecystokinin and gastrin.</Title>
-<Xref>DOI:10.1016/0006-291X(86)91098-3</Xref>
-<Xref>PMID:3778455</Xref>
-<Note>chromatographic detection; mass spectrometric identification; chemical synthesis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hortin, G.</Author>
-<Author>Folz, R.</Author>
-<Author>Gordon, J.I.</Author>
-<Author>Strauss, A.W.</Author>
-</Authors>
-<Citation>Biochem. Biophys. Res. Commun. 141, 326-333, 1986</Citation>
-<Title>Characterization of sites of tyrosine sulfation in proteins and criteria for predicting their occurrence.</Title>
-<Xref>DOI:10.1016/S0006-291X(86)80372-2</Xref>
-<Xref>PMID:3801003</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Johnsen, A.H.</Author>
-<Author>Rehfeld, J.F.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 265, 3054-3058, 1990</Citation>
-<Title>Cionin: a disulfotyrosyl hybrid of cholecystokinin and gastrin from the neural ganglion of the protochordate Ciona intestinalis.</Title>
-<Xref>PMID:2303439</Xref>
-<Note>sulfotyrosyl-sulfotyrosyl sequence confirmed by enzymatic analysis and synthesis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wolfender, J.L.</Author>
-<Author>Chu, F.</Author>
-<Author>Ball, H.</Author>
-<Author>Wolfender, F.</Author>
-<Author>Fainzilber, M.</Author>
-<Author>Baldwin, M.A.</Author>
-<Author>Burlingame, A.L.</Author>
-</Authors>
-<Citation>J. Mass Spectrom. 34, 447-454, 1999</Citation>
-<Title>Identification of tyrosine sulfation in Conus pennaceus conotoxins alpha-PnIA and alpha-PnIB: further investigation of labile sulfo- and phosphopeptides by electrospray, matrix-assisted laser desorption/ionization (MALDI) and atmospheric pressure MALDI mass spectrometry.</Title>
-<Xref>DOI:10.1002/(SICI)1096-9888(199904)34:4&lt;447::AID-JMS801&gt;3.3.CO;2-T</Xref>
-<Xref>PMID:10226369</Xref>
-<Note>attempt to distinguish between the essentially isobaric protonated forms of phosphotyrosine (see RESID:AA0039) and sulfotyrosine by negative ion mode MALDI</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>protein-tyrosine sulfotransferase (EC 2.8.2.20)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>Y</SequenceSpec>
-<Xref>GO:0006478</Xref>
-<Xref>PSI-MOD:00181</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>sulfoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__sulfotyrosine__y">MOD_RES Sulfotyrosine</Feature>
-</Features>
-<Image src="/images/AA0172.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0172.PDB" />
-</Entry>
-<Entry id="AA0173">
-<Header>
-<Code>AA0173</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Sep-2008</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-bromohistidine</Name>
-</Names>
-<FormulaBlock>
-<Formula>Br 1 C 6 H 6 N 3 O 1</Formula>
-<Weight type="chemical">216.04</Weight>
-<Weight type="physical">214.969424</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0009">
-<Formula>Br 1 C 0 H -1 N 0 O 0</Formula>
-<Weight type="chemical">78.90</Weight>
-<Weight type="physical">77.910512</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Takao, T.</Author>
-<Author>Yoshino, K.</Author>
-<Author>Suzuki, N.</Author>
-<Author>Shimonishi, Y.</Author>
-</Authors>
-<Citation>Biomed. Environ. Mass Spectrom. 19, 705-712, 1990</Citation>
-<Title>Analysis of post-translational modifications of proteins by accurate mass measurement in fast atom bombardment mass spectrometry.</Title>
-<Xref>DOI:10.1002/bms.1200191109</Xref>
-<Xref>PMID:2076468</Xref>
-<Note>mass spectrometric identification</Note>
-</ReferenceBlock>
-<Comment>The position of the bromine substitution is uncertain. The 2'-bromohistidine is shown.</Comment>
-<SequenceCode>
-<SequenceSpec>H</SequenceSpec>
-<Xref>GO:0018074</Xref>
-<Xref>PSI-MOD:00182</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>bromine</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__bromohistidine__h">MOD_RES Bromohistidine</Feature>
-</Features>
-<Image src="/images/AA0173.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0173.PDB" />
-</Entry>
-<Entry id="AA0174">
-<Header>
-<Code>AA0174</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Sep-2008</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-2'-bromophenylalanine</Name>
-<AlternateName>o-bromophenylalanine</AlternateName>
-<AlternateName>ortho-bromophenylalanine</AlternateName>
-<SystematicName>(S)-2-amino-3-(2-bromophenyl)propanoic acid</SystematicName>
-<Xref>CAS:42538-40-9</Xref>
-</Names>
-<FormulaBlock>
-<Formula>Br 1 C 9 H 8 N 1 O 1</Formula>
-<Weight type="chemical">226.07</Weight>
-<Weight type="physical">224.978926</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0014">
-<Formula>Br 1 C 0 H -1 N 0 O 0</Formula>
-<Weight type="chemical">78.90</Weight>
-<Weight type="physical">77.910512</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yoshino, K.</Author>
-<Author>Takao, T.</Author>
-<Author>Suhara, M.</Author>
-<Author>Kitai, T.</Author>
-<Author>Hori, H.</Author>
-<Author>Nomura, K.</Author>
-<Author>Yamaguchi, M.</Author>
-<Author>Shimonishi, Y.</Author>
-<Author>Suzuki, N.</Author>
-</Authors>
-<Citation>Biochemistry 30, 6203-6209, 1991</Citation>
-<Title>Identification of a novel amino acid, o-bromo-L-phenylalanine, in egg-associated peptides that activate spermatozoa.</Title>
-<Xref>DOI:10.1021/bi00239a018</Xref>
-<Xref>PMID:2059627</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Takao, T.</Author>
-<Author>Yoshino, K.</Author>
-<Author>Suzuki, N.</Author>
-<Author>Shimonishi, Y.</Author>
-</Authors>
-<Citation>Biomed. Environ. Mass Spectrom. 19, 705-712, 1990</Citation>
-<Title>Analysis of post-translational modifications of proteins by accurate mass measurement in fast atom bombardment mass spectrometry.</Title>
-<Xref>DOI:10.1002/bms.1200191109</Xref>
-<Xref>PMID:2076468</Xref>
-<Note>chromatographic and mass spectrometric identification; chemical synthesis</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>F</SequenceSpec>
-<Xref>GO:0018075</Xref>
-<Xref>GO:0018397</Xref>
-<Xref>PSI-MOD:00183</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>bromine</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0174.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0174.PDB" />
-</Entry>
-<Entry id="AA0175">
-<Header>
-<Code>AA0175</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Sep-2008</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-3'-bromophenylalanine</Name>
-<AlternateName>m-bromophenylalanine</AlternateName>
-<AlternateName>meta-bromophenylalanine</AlternateName>
-<SystematicName>(S)-2-amino-3-(3-bromophenyl)propanoic acid</SystematicName>
-<Xref>CAS:82311-69-1</Xref>
-</Names>
-<FormulaBlock>
-<Formula>Br 1 C 9 H 8 N 1 O 1</Formula>
-<Weight type="chemical">226.07</Weight>
-<Weight type="physical">224.978926</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0014">
-<Formula>Br 1 C 0 H -1 N 0 O 0</Formula>
-<Weight type="chemical">78.90</Weight>
-<Weight type="physical">77.910512</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Takao, T.</Author>
-<Author>Yoshino, K.</Author>
-<Author>Suzuki, N.</Author>
-<Author>Shimonishi, Y.</Author>
-</Authors>
-<Citation>Biomed. Environ. Mass Spectrom. 19, 705-712, 1990</Citation>
-<Title>Analysis of post-translational modifications of proteins by accurate mass measurement in fast atom bombardment mass spectrometry.</Title>
-<Xref>DOI:10.1002/bms.1200191109</Xref>
-<Xref>PMID:2076468</Xref>
-<Note>chemical synthesis</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>F</SequenceSpec>
-<Xref>GO:0018075</Xref>
-<Xref>GO:0018398</Xref>
-<Xref>PSI-MOD:00184</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>bromine</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0175.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0175.PDB" />
-</Entry>
-<Entry id="AA0176">
-<Header>
-<Code>AA0176</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-Dec-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-4'-bromophenylalanine</Name>
-<AlternateName>p-bromophenylalanine</AlternateName>
-<AlternateName>para-bromophenylalanine</AlternateName>
-<SystematicName>(2S)-2-amino-3-(4-bromophenyl)propanoic acid</SystematicName>
-<Xref>CAS:24250-84-8</Xref>
-<Xref>PDBHET:4BF</Xref>
-</Names>
-<FormulaBlock>
-<Formula>Br 1 C 9 H 8 N 1 O 1</Formula>
-<Weight type="chemical">226.07</Weight>
-<Weight type="physical">224.978926</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0014">
-<Formula>Br 1 C 0 H -1 N 0 O 0</Formula>
-<Weight type="chemical">78.90</Weight>
-<Weight type="physical">77.910512</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Takao, T.</Author>
-<Author>Yoshino, K.</Author>
-<Author>Suzuki, N.</Author>
-<Author>Shimonishi, Y.</Author>
-</Authors>
-<Citation>Biomed. Environ. Mass Spectrom. 19, 705-712, 1990</Citation>
-<Title>Analysis of post-translational modifications of proteins by accurate mass measurement in fast atom bombardment mass spectrometry.</Title>
-<Xref>DOI:10.1002/bms.1200191109</Xref>
-<Xref>PMID:2076468</Xref>
-<Note>chemical synthesis</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>F</SequenceSpec>
-<Xref>GO:0018075</Xref>
-<Xref>GO:0018399</Xref>
-<Xref>PSI-MOD:00185</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>bromine</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0176.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0176.PDB" />
-</Entry>
-<Entry id="AA0177">
-<Header>
-<Code>AA0177</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>3',3'',5'-triiodo-L-thyronine</Name>
-<AlternateName>3,3',5-triiodo-L-thyronine</AlternateName>
-<AlternateName>3,5,3'-triiodo-L-thyronine</AlternateName>
-<AlternateName>4-(4-hydroxy-3-iodophenoxy)-3,5-diiodo-L-phenylalanine</AlternateName>
-<AlternateName>liothyronine</AlternateName>
-<AlternateName>O-(4-hydroxy-3-iodophenyl)-3,5-diiodo-L-tyrosine</AlternateName>
-<AlternateName>T3</AlternateName>
-<SystematicName>(S)-2-amino-3-[4-(4-hydroxy-3-iodophenoxy)-3,5-diiodophenyl]propanoic acid</SystematicName>
-<Xref>CAS:6893-02-3</Xref>
-<Xref>ChEBI:90874</Xref>
-<Xref>PDBHET:T3</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 15 H 10 I 3 N 1 O 3</Formula>
-<Weight type="chemical">632.96</Weight>
-<Weight type="physical">632.779486</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0019">
-<Formula>C 6 H 1 I 3 N 0 O 1</Formula>
-<Weight type="chemical">469.79</Weight>
-<Weight type="physical">469.716158</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Marriq, C.</Author>
-<Author>Rolland, M.</Author>
-<Author>Lissitzky, S.</Author>
-</Authors>
-<Citation>Biochem. Biophys. Res. Commun. 112, 206-213, 1983</Citation>
-<Title>Amino acid sequence of the unique 3,5,3'-triiodothyronine-containing sequence from porcine thyroglobulin.</Title>
-<Xref>DOI:10.1016/0006-291X(83)91817-X </Xref>
-<Xref>PMID:6838607</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Salek, M.</Author>
-<Author>Lehmann, W.D.</Author>
-</Authors>
-<Citation>Proteomics 5, 351-353, 2005</Citation>
-<Title>Analysis of thyroglobulin iodination by tandem mass spectrometry using immonium ions of monoiodo- and diiodo-tyrosine.</Title>
-<Xref>DOI:10.1002/pmic.200400949</Xref>
-<Xref>PMID:15627961</Xref>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>Y</SequenceSpec>
-<Xref>GO:0018078</Xref>
-<Xref>GO:0018407</Xref>
-<Xref>PSI-MOD:00186</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>iodine</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__triiodothyronine__y">MOD_RES Triiodothyronine</Feature>
-</Features>
-<Image src="/images/AA0177.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0177.PDB" />
-</Entry>
-<Entry id="AA0178">
-<Header>
-<Code>AA0178</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-thyroxine</Name>
-<AlternateName>3',3'',5',5''-tetraiodo-L-thyronine</AlternateName>
-<AlternateName>3,3',5,5'-tetraiodo-L-thyronine</AlternateName>
-<AlternateName>3,5,3',5'-tetraiodo-L-thyronine</AlternateName>
-<AlternateName>4-(4-hydroxy-3,5-diiodophenoxy)-3,5-diiodo-L-phenylalanine</AlternateName>
-<AlternateName>O-(4-hydroxy-3,5-diiodophenyl)-3,5-diiodo-L-tyrosine</AlternateName>
-<AlternateName>T4</AlternateName>
-<SystematicName>(S)-2-amino-3-[4-(4-hydroxy-3,5-diiodophenoxy)-3,5-diiodophenyl]propanoic acid</SystematicName>
-<Xref>CAS:51-48-9</Xref>
-<Xref>ChEBI:90872</Xref>
-<Xref>PDBHET:T44</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 15 H 9 I 4 N 1 O 3</Formula>
-<Weight type="chemical">758.86</Weight>
-<Weight type="physical">758.676134</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0019">
-<Formula>C 6 H 0 I 4 N 0 O 1</Formula>
-<Weight type="chemical">595.68</Weight>
-<Weight type="physical">595.612805</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Rawitch, A.B.</Author>
-<Author>Litwer, M.R.</Author>
-<Author>Gregg, J.</Author>
-<Author>Turner, C.D.</Author>
-<Author>Rouse, J.B.</Author>
-<Author>Hamilton, J.W.</Author>
-</Authors>
-<Citation>Biochem. Biophys. Res. Commun. 118, 423-429, 1984</Citation>
-<Title>The isolation of identical thyroxine containing amino acid sequences from bovine, ovine and porcine thyroglobulins.</Title>
-<Xref>DOI:10.1016/0006-291X(84)91320-2</Xref>
-<Xref>PMID:6704086</Xref>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>Y</SequenceSpec>
-<Xref>GO:0018078</Xref>
-<Xref>GO:0018408</Xref>
-<Xref>PSI-MOD:00187</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>iodine</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__thyroxine__y">MOD_RES Thyroxine</Feature>
-</Features>
-<Image src="/images/AA0178.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0178.PDB" />
-</Entry>
-<Entry id="AA0179">
-<Header>
-<Code>AA0179</Code>
-<Dates>
-<CreationDate>28-Feb-1997</CreationDate>
-<StrucRevDate>28-Feb-1997</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>6'-bromo-L-tryptophan</Name>
-<SystematicName>(2S)-2-amino-3-(6-bromo-1H-indol-3-yl)propanoic acid</SystematicName>
-<Xref>CAS:52448-17-6</Xref>
-<Xref>ChEBI:61899</Xref>
-<Xref>PDBHET:BTR</Xref>
-</Names>
-<FormulaBlock>
-<Formula>Br 1 C 11 H 9 N 2 O 1</Formula>
-<Weight type="chemical">265.11</Weight>
-<Weight type="physical">263.989825</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0018">
-<Formula>Br 1 C 0 H -1 N 0 O 0</Formula>
-<Weight type="chemical">78.90</Weight>
-<Weight type="physical">77.910512</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Jimenez, E.C.</Author>
-<Author>Craig, A.G.</Author>
-<Author>Watkins, M.</Author>
-<Author>Hillyard, D.R.</Author>
-<Author>Gray, W.R.</Author>
-<Author>Gulyas, J.</Author>
-<Author>Rivier, J.E.</Author>
-<Author>Cruz, L.J.</Author>
-<Author>Olivera, B.M.</Author>
-</Authors>
-<Citation>Biochemistry 36, 989-994, 1997</Citation>
-<Title>Bromocontryphan: post-translational bromination of tryptophan.</Title>
-<Xref>DOI:10.1021/bi962840p</Xref>
-<Xref>PMID:9033387</Xref>
-<Note>mass spectrometric detection; chromatographic characterization; chemical synthesis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Craig, A.G.</Author>
-<Author>Jimenez, E.C.</Author>
-<Author>Dykert, J.</Author>
-<Author>Nielsen, D.B.</Author>
-<Author>Gulyas, J.</Author>
-<Author>Abogadie, F.C.</Author>
-<Author>Porter, J.</Author>
-<Author>Rivier, J.E.</Author>
-<Author>Cruz, L.J.</Author>
-<Author>Olivera, B.M.</Author>
-<Author>McIntosh, J.M.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 272, 4689-4698, 1997</Citation>
-<Title>A novel post-translational modification involving bromination of tryptophan. Identification of the residue, L-6-bromotryptophan, in peptides from Conus imperialis and Conus radiatus venom.</Title>
-<Xref>DOI:10.1074/jbc.272.8.4689</Xref>
-<Xref>PMID:9030520</Xref>
-<Note>mass spectrometric detection; chromatographic characterization; chemical synthesis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Taylor, S.W.</Author>
-<Author>Kammerer, B.</Author>
-<Author>Nicholson, G.J.</Author>
-<Author>Pusecker, K.</Author>
-<Author>Walk, T.</Author>
-<Author>Bayer, E.</Author>
-<Author>Scippa, S.</Author>
-<Author>de Vincentiis, M.</Author>
-</Authors>
-<Citation>Arch. Biochem. Biophys. 348, 278-288, 1997</Citation>
-<Title>Morulin Pm: a modified polypeptide containing TOPA and 6-bromotryptophan from the morula cells of the ascidian, Phallusia mammillata.</Title>
-<Xref>DOI:10.1006/abbi.1997.0371</Xref>
-<Xref>PMID:9434739</Xref>
-<Note>(1)H-NMR and (13)C-NMR characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Rigby, A.C.</Author>
-<Author>Lucas-Meunier, E.</Author>
-<Author>Kalume, D.E.</Author>
-<Author>Czerwiec, E.</Author>
-<Author>Hambe, B.</Author>
-<Author>Dahlqvist, I.</Author>
-<Author>Fossier, P.</Author>
-<Author>Baux, G.</Author>
-<Author>Roepstorff, P.</Author>
-<Author>Baleja, J.D.</Author>
-<Author>Furie, B.C.</Author>
-<Author>Furie, B.</Author>
-<Author>Stenflo, J.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 96, 5758-5763, 1999</Citation>
-<Title>A conotoxin from Conus textile with unusual posttranslational modifications reduces presynaptic Ca2+ influx.</Title>
-<Xref>DOI:10.1073/pnas.96.10.5758</Xref>
-<Xref>PMID:10318957</Xref>
-<Note>mass spectrometric and (1)H-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Rigby, A.C.</Author>
-<Author>Hambe, B.</Author>
-<Author>Czerwiec, E.</Author>
-<Author>Baleja, J.D.</Author>
-<Author>Furie, B.C.</Author>
-<Author>Furie, B.</Author>
-<Author>Stenflo, J.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, June 1999</Citation>
-<Description>A novel conotoxin from Conus textile with unusual post-translational modifications reduces presynaptic calcium influx, NMR, 1 structure, glycosylated protein.</Description>
-<Xref>PDB:1WCT</Xref>
-<Note>conformation by (1)H-NMR</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fujii, R.</Author>
-<Author>Yoshida, H.</Author>
-<Author>Fukusumi, S.</Author>
-<Author>Habata, Y.</Author>
-<Author>Hosoya, M.</Author>
-<Author>Kawamata, Y.</Author>
-<Author>Yano, T.</Author>
-<Author>Hinuma, S.</Author>
-<Author>Kitada, C.</Author>
-<Author>Asami, T.</Author>
-<Author>Mori, M.</Author>
-<Author>Fujisawa, Y.</Author>
-<Author>Fujino, M.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 277, 34010-34016, 2002</Citation>
-<Title>Identification of a neuropeptide modified with bromine as an endogenous ligand for GPR7.</Title>
-<Xref>DOI:10.1074/jbc.M205883200</Xref>
-<Xref>PMID:12118011</Xref>
-<Note>identification of an edogenous ligand for an "orphan" G protein-coupled receptor</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>W</SequenceSpec>
-<Xref>GO:0018080</Xref>
-<Xref>PSI-MOD:00188</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>bromine</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__6&apos;-bromotryptophan__w">MOD_RES 6'-bromotryptophan</Feature>
-</Features>
-<Image src="/images/AA0179.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0179.PDB" />
-</Entry>
-<Entry id="AA0180">
-<Header>
-<Code>AA0180</Code>
-<Dates>
-<CreationDate>31-Dec-2006</CreationDate>
-<StrucRevDate>31-Dec-2006</StrucRevDate>
-<TextChngDate>31-Dec-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>6'-chloro-L-tryptophan</Name>
-<SystematicName>(2S)-2-amino-3-(6-chloro-1H-indol-3-yl)propanoic acid</SystematicName>
-<Xref>CAS:17808-35-4</Xref>
-<Xref>PDBHET:6CW</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 11 Cl 1 H 9 N 2 O 1</Formula>
-<Weight type="chemical">220.66</Weight>
-<Weight type="physical">220.040341</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0018">
-<Formula>C 0 Cl 1 H -1 N 0 O 0</Formula>
-<Weight type="chemical">34.44</Weight>
-<Weight type="physical">33.961028</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lazzarini, A.</Author>
-<Author>Gastaldo, L.</Author>
-<Author>Candiani, G.</Author>
-<Author>Ciciliato, I.</Author>
-<Author>Losi, D.</Author>
-<Author>Marinelli, F.</Author>
-<Author>Selva, E.</Author>
-<Author>Parenti, F.</Author>
-</Authors>
-<Citation type="submission">submitted to the European Patent Office, 17 February 2005</Citation>
-<Description>Antibiotic 107891, its factors A1 and A2, pharmaceutically acceptable salts and compositions, and use thereof.</Description>
-<Xref>EPO:EP1646646</Xref>
-<Xref>WIPO:WO2005014628</Xref>
-<Note>mass spectrometric and (1)H-NMR identification</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>W</SequenceSpec>
-<Xref>PSI-MOD:00886</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chlorine</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__6&apos;-chlorotryptophan__w">MOD_RES 6'-chlorotryptophan</Feature>
-</Features>
-<Image src="/images/AA0180.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0180.PDB" />
-</Entry>
-<Entry id="AA0181">
-<Header>
-<Code>AA0181</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>13-Sep-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>dehydroalanine</Name>
-<AlternateName>2,3-didehydroalanine</AlternateName>
-<AlternateName>2-aminoacrylic acid</AlternateName>
-<AlternateName>4-methylidene-imidazole-5-one (MIO) active site</AlternateName>
-<AlternateName>anhydroserine</AlternateName>
-<AlternateName>Dha</AlternateName>
-<SystematicName>2-aminopropenoic acid</SystematicName>
-<Xref>CAS:1948-56-7</Xref>
-<Xref>ChEBI:17123</Xref>
-<Xref>PDBHET:DHA</Xref>
-<Xref>PDBHET:MDO</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 3 N 1 O 1</Formula>
-<Weight type="chemical">69.06</Weight>
-<Weight type="physical">69.021464</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005" label="CYS">
-<Formula>C 0 H -2 N 0 O 0 S -1</Formula>
-<Weight type="chemical">-34.08</Weight>
-<Weight type="physical">-33.987721</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0022" label="SEC">
-<Formula>C 0 H -2 N 0 O 0 Se -1</Formula>
-<Weight type="chemical">-80.99</Weight>
-<Weight type="physical">-81.932171</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0016" label="SER">
-<Formula>C 0 H -2 N 0 O -1</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0019" label="TYR">
-<Formula>C -6 H -6 N 0 O -1</Formula>
-<Weight type="chemical">-94.11</Weight>
-<Weight type="physical">-94.041865</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Marriq, C.</Author>
-<Author>Lejeune, P.J.</Author>
-<Author>Venot, N.</Author>
-<Author>Vinet, L.</Author>
-</Authors>
-<Citation>FEBS Lett. 242, 414-418, 1989</Citation>
-<Title>Hormone synthesis in human thyroglobulin: possible cleavage of the polypeptide chain at the tyrosine donor site.</Title>
-<Xref>DOI:10.1016/0014-5793(89)80513-7</Xref>
-<Xref>PMID:2914619</Xref>
-<Note>formation of thyroxine and dehydroalanine by tyrosine ring donation</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bartone, N.A.</Author>
-<Author>Bentley, J.D.</Author>
-<Author>Maclaren, J.A.</Author>
-</Authors>
-<Citation>J. Protein Chem. 10, 603-607, 1991</Citation>
-<Title>Determination of dehydroalanine residues in proteins and peptides: an improved method.</Title>
-<Xref>DOI:10.1007/BF01025712</Xref>
-<Xref>PMID:1815586</Xref>
-<Note>conversion with 4-pyridoethanethiol to 4-pyridoethyl cysteine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Chan, W.C.</Author>
-<Author>Bycroft, B.W.</Author>
-<Author>Leyland, M.L.</Author>
-<Author>Lian, L.Y.</Author>
-<Author>Yang, J.C.</Author>
-<Author>Roberts, G.C.K.</Author>
-</Authors>
-<Citation>FEBS Lett. 300, 56-62, 1992</Citation>
-<Title>Sequence-specific resonance assignment and conformational analysis of subtilin by 2D NMR.</Title>
-<Xref>DOI:10.1016/0014-5793(92)80163-B</Xref>
-<Xref>PMID:1547888</Xref>
-<Note>(1)H-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hernandez, D.</Author>
-<Author>Stroh, J.G.</Author>
-<Author>Phillips, A.T.</Author>
-</Authors>
-<Citation>Arch. Biochem. Biophys. 307, 126-132, 1993</Citation>
-<Title>Identification of Ser(143) as the site of modification in the active site of histidine ammonia-lyase.</Title>
-<Xref>DOI:10.1006/abbi.1993.1570</Xref>
-<Xref>PMID:8239649</Xref>
-<Note>mass spectrometric and UV spectrographic characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Langer, M.</Author>
-<Author>Lieber, A.</Author>
-<Author>Retey, J.</Author>
-</Authors>
-<Citation>Biochemistry 33, 14034-14038, 1994</Citation>
-<Title>Histidine ammonia-lyase mutant S143C is posttranslationally converted into fully active wild-type enzyme. Evidence for serine 143 to be the precursor of active site dehydroalanine.</Title>
-<Xref>DOI:10.1021/bi00251a011</Xref>
-<Xref>PMID:7947813</Xref>
-<Note>mutational analysis; no chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Schwede, T.F.</Author>
-<Author>Retey, J.</Author>
-<Author>Schulz, G.E.</Author>
-</Authors>
-<Citation>Biochemistry 38, 5355-5361, 1999</Citation>
-<Title>Crystal structure of histidine ammonia-lyase revealing a novel polypeptide modification as the catalytic electrophile.</Title>
-<Xref>DOI:10.1021/bi982929q</Xref>
-<Xref>PMID:10220322</Xref>
-<Note>X-ray diffraction, 2.1 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ma, S.</Author>
-<Author>Caprioli, R.M.</Author>
-<Author>Hill, K.E.</Author>
-<Author>Burk, R.F.</Author>
-</Authors>
-<Citation>J. Am. Soc. Mass Spectrom. 14, 593-600, 2003</Citation>
-<Title>Loss of selenium from selenoproteins: conversion of selenocysteine to dehydroalanine in vitro.</Title>
-<Xref>DOI:10.1016/S1044-0305(03)00141-7</Xref>
-<Xref>PMID:12781460</Xref>
-<Note>observation of artifactual conversion of seleocysteine to dehydroalanine </Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Claesen, J.</Author>
-<Author>Bibb, M.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 107, 16297-16302, 2010</Citation>
-<Title>Genome mining and genetic analysis of cypemycin biosynthesis reveal an unusual class of posttranslationally modified peptides.</Title>
-<Xref>DOI:10.1073/pnas.1008608107</Xref>
-<Xref>PMID:20805503</Xref>
-<Note>gene sequence for the encoded peptide, biosynthesis as an intermediate from cysteine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Chatterjee, A.</Author>
-<Author>Abeydeera, N.D.</Author>
-<Author>Bale, S.</Author>
-<Author>Pai, P.J.</Author>
-<Author>Dorrestein, P.C.</Author>
-<Author>Russell, D.H.</Author>
-<Author>Ealick, S.E.</Author>
-<Author>Begley, T.P.</Author>
-</Authors>
-<Citation>Nature 478, 542-546, 2011</Citation>
-<Title>Saccharomyces cerevisiae THI4p is a suicide thiamine thiazole synthase.</Title>
-<Xref>DOI:10.1038/nature10503</Xref>
-<Xref>PMID:22031445</Xref>
-<Note>X-ray diffraction, 1.82 angstroms; one protein molecule is shown to synthesize a thiazole for thiamine from NAD by donating a sulfur from a peptide cysteine and forming dehydroalanine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bale, S.</Author>
-<Author>Chatterjee, A.</Author>
-<Author>Dorrestein, P.C.</Author>
-<Author>Begley, T.P.</Author>
-<Author>Ealick, S.E.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, January 2009</Citation>
-<Description>Saccharomyces cerevisiae THI4p is a suicide thiamin thiazole synthase.</Description>
-<Xref>PDB:3FPZ</Xref>
-<Note>X-ray diffraction, 1.82 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wang, S.K.</Author>
-<Author>Weaver, J.D.</Author>
-<Author>Zhang, S.</Author>
-<Author>Lei, X.G.</Author>
-</Authors>
-<Citation>Free Radic. Biol. Med. 51, 197-204, 2011</Citation>
-<Title>Knockout of SOD1 promotes conversion of selenocysteine to dehydroalanine in murine hepatic GPX1 protein.</Title>
-<Xref>DOI:10.1016/j.freeradbiomed.2011.03.018</Xref>
-<Xref>PMID:21420488</Xref>
-<Note>deselenation of seleocysteine to dehydroalanine in glutathione peroxidase-1 caused by superoxide radical accumulating in the absence of superoxide dismutase</Note>
-</ReferenceBlock>
-<Comment>The modification of serine to dehydroalanine coupled with the formation of 5-imidazolinone by the two neighboring residues produces the 4-methylidene-imidazole-5-one (MIO) active site of some amino acid ammonia-lyases that differs by UV and mass spectrometric evidence from other known dehydroalanine containing peptides not containing the second modification.</Comment>
-<Comment>The formation of iodinated thyronine, O-(4-hydroxyphenyl)-tyrosine, by phenoxy radical transfer from tyrosine in thyroglobulin produces dehydroalanine as a by-product. See RESID:AA0177 and RESID:AA0178.</Comment>
-<Comment>The formation of S-(2-aminovinyl)-L-cysteine, see RESID:AA0548, requires that an interior cysteine first undergoes oxidative dethiolation to form dehydroalanine. This reaction is normally followed by formation of an L-lanthionine through reformation of an L-cysteine in a thioether bond with the C-terminal cysteine. The C-terminal cysteine is subsequently decarboxylated. Because the intermediate dehydroalanine formed from cysteine is not normally observed, it is not annotated as a feature in UniProt.</Comment>
-<Comment>Either free or in a peptide chain, dehydroalanine is unstable, undergoing hydrolysis with formation of 2-hydroxyalanine which can, like 2-hydroxyglycine (see RESID:AA0434), decompose by deamination breaking the peptide backbone to form a peptide amide and a pyruvoyl peptide (see RESID:AA0127). A 2,3-didehydro amino acid blocks Edman degradation.</Comment>
-<GeneratingEnzyme>
-<EnzymeName link="CYS">protein-cysteine dethiolase (EC 4.4.1.-)</EnzymeName>
-<EnzymeName link="SEC">autocatalytic</EnzymeName>
-<EnzymeName link="SER">protein-serine dehydratase (EC 4.2.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode link="CYS">
-<SequenceSpec>C</SequenceSpec>
-<Xref>PSI-MOD:00793</Xref>
-<Xref>PSI-MOD:01168</Xref>
-</SequenceCode>
-<SequenceCode link="SEC">
-<SequenceSpec>U</SequenceSpec>
-<Xref>PSI-MOD:01954</Xref>
-</SequenceCode>
-<SequenceCode link="SER">
-<SequenceSpec>S</SequenceSpec>
-<Condition>incidental to RESID:AA0187</Condition>
-<Condition>incidental to RESID:AA0188</Condition>
-<Xref>PSI-MOD:00189</Xref>
-<Xref>PSI-MOD:01168</Xref>
-</SequenceCode>
-<SequenceCode link="TYR">
-<SequenceSpec>Y</SequenceSpec>
-<Condition>incidental to RESID:AA0178</Condition>
-<Xref>GO:0018250</Xref>
-<Xref>PSI-MOD:00824</Xref>
-<Xref>PSI-MOD:01168</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="mod_res__2,3-didehydroalanine (ser)__s" link="SER">MOD_RES 2,3-didehydroalanine (Ser)</Feature>
-<Feature type="UniProt" key="mod_res__2,3-didehydroalanine (cys)__c" link="CYS">MOD_RES 2,3-didehydroalanine (Cys)</Feature>
-</Features>
-<Image src="/images/AA0181.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0181.PDB" />
-</Entry>
-<Entry id="AA0182">
-<Header>
-<Code>AA0182</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>13-Sep-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>(Z)-dehydrobutyrine</Name>
-<AlternateName>(Z)-2-amino-2-butenoic acid</AlternateName>
-<AlternateName>(Z)-2-aminobutenoic acid</AlternateName>
-<AlternateName>2,3-didehydrobutyrine</AlternateName>
-<AlternateName>3-methyldehydroalanine</AlternateName>
-<AlternateName>alpha,beta-dehydroaminobutyric acid</AlternateName>
-<AlternateName>anhydrothreonine</AlternateName>
-<AlternateName>Dhb</AlternateName>
-<AlternateName>methyl-dehydroalanine</AlternateName>
-<SystematicName>(2Z)-2-aminobut-2-enoic acid</SystematicName>
-<Xref>CAS:71018-10-5</Xref>
-<Xref>PDBHET:DBU</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 5 N 1 O 1</Formula>
-<Weight type="chemical">83.09</Weight>
-<Weight type="physical">83.037114</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0017">
-<Formula>C 0 H -2 N 0 O -1</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Allgaier, H.</Author>
-<Author>Jung, G.</Author>
-<Author>Werner, R.G.</Author>
-<Author>Schneider, U.</Author>
-<Author>Zaehner, H.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 160, 9-22, 1986</Citation>
-<Title>Epidermin: sequencing of a heterodet tetracyclic 21-peptide amide antibiotic.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1986.tb09933.x</Xref>
-<Xref>PMID:3769923</Xref>
-<Note>(1)H-NMR and (13)C-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Chan, W.C.</Author>
-<Author>Bycroft, B.W.</Author>
-<Author>Leyland, M.L.</Author>
-<Author>Lian, L.Y.</Author>
-<Author>Yang, J.C.</Author>
-<Author>Roberts, G.C.K.</Author>
-</Authors>
-<Citation>FEBS Lett. 300, 56-62, 1992</Citation>
-<Title>Sequence-specific resonance assignment and conformational analysis of subtilin by 2D NMR.</Title>
-<Xref>DOI:10.1016/0014-5793(92)80163-B</Xref>
-<Xref>PMID:1547888</Xref>
-<Note>(1)H-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Piard, J.C.</Author>
-<Author>Kuipers, O.P.</Author>
-<Author>Rollema, H.S.</Author>
-<Author>Desmazeaud, M.J.</Author>
-<Author>de Vos, W.M.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 268, 16361-16368, 1993</Citation>
-<Title>Structure, organization, and expression of the lct gene for lacticin 481, a novel lantibiotic produced by Lactococcus lactis.</Title>
-<Xref>PMID:8344922</Xref>
-<Note>the (E)- and (Z)-isomers are distinguished by (1)H-NOE NMR</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Li, H.</Author>
-<Author>Xu, H.</Author>
-<Author>Zhou, Y.</Author>
-<Author>Zhang, J.</Author>
-<Author>Long, C.</Author>
-<Author>Li, S.</Author>
-<Author>Chen, S.</Author>
-<Author>Zhou, J.M.</Author>
-<Author>Shao, F.</Author>
-</Authors>
-<Citation>Science 315, 1000-1003, 2007</Citation>
-<Title>The phosphothreonine lyase activity of a bacterial type III effector family.</Title>
-<Xref>DOI:10.1126/science.1138960</Xref>
-<Xref>PMID:17303758</Xref>
-<Note>mass spectrometric identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Shenkarev, Z.O.</Author>
-<Author>Finkina, E.I.</Author>
-<Author>Nurmukhamedova, E.K.</Author>
-<Author>Balandin, S.V.</Author>
-<Author>Mineev, K.S.</Author>
-<Author>Nadezhdin, K.D.</Author>
-<Author>Yakimenko, Z.A.</Author>
-<Author>Tagaev, A.A.</Author>
-<Author>Temirov, Y.V.</Author>
-<Author>Arseniev, A.S.</Author>
-<Author>Ovchinnikova, T.V.</Author>
-</Authors>
-<Citation>Biochemistry 49, 6462-6472, 2010</Citation>
-<Title>Isolation, structure elucidation, and synergistic antibacterial activity of a novel two-component lantibiotic lichenicidin from Bacillus licheniformis VK21.</Title>
-<Xref>DOI:10.1021/bi100871b</Xref>
-<Xref>PMID:20578714</Xref>
-<Note>the (E)- and (Z)- isomers are distinguished by (1)H-NOE NMR</Note>
-</ReferenceBlock>
-<Comment>In some cases it has not been firmly established whether the natural form is the Z or the E isomer. For the E isomer, see RESID:AA0547.</Comment>
-<Comment>A 2,3-didehydro amino acid blocks Edman degradation.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>protein-threonine dehydratase (EC 4.2.1.-)</EnzymeName>
-<EnzymeName>phosphothreonine lyase (EC 4.3.2.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>T</SequenceSpec>
-<Xref>GO:0018082</Xref>
-<Xref>PSI-MOD:00190</Xref>
-<Xref>PSI-MOD:01471</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="mod_res__(z)-2,3-didehydrobutyrine__t">MOD_RES (Z)-2,3-didehydrobutyrine</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="mod_res__2,3-didehydrobutyrine__t">MOD_RES 2,3-didehydrobutyrine</Feature>
-<Note>this UniProt feature is used when the stereochemistry has not been determined</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0182.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0182.PDB" />
-</Entry>
-<Entry id="AA0183">
-<Header>
-<Code>AA0183</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>(Z)-2,3-didehydrotyrosine</Name>
-<AlternateName>amino-(para-hydroxybenzylidenyl)acetic acid</AlternateName>
-<AlternateName>cis-dehydrotyrosine</AlternateName>
-<AlternateName>green fluorescent protein chromophore</AlternateName>
-<AlternateName>para-hydroxybenzylidene-imidazolidinone chromophore</AlternateName>
-<AlternateName>red fluorescent protein chromophore</AlternateName>
-<SystematicName>(2Z)-2-amino-3-(4-hydroxyphenyl)prop-2-enoic acid</SystematicName>
-<Xref>PDBHET:CH6</Xref>
-<Xref>PDBHET:CRO</Xref>
-<Xref>PDBHET:CRQ</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 7 N 1 O 2</Formula>
-<Weight type="chemical">161.16</Weight>
-<Weight type="physical">161.047678</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0019">
-<Formula>C 0 H -2 N 0 O 0</Formula>
-<Weight type="chemical">-2.02</Weight>
-<Weight type="physical">-2.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Prasher, D.C.</Author>
-<Author>Eckenrode, V.K.</Author>
-<Author>Ward, W.W.</Author>
-<Author>Prendergast, F.G.</Author>
-<Author>Cormier, M.J.</Author>
-</Authors>
-<Citation>Gene 111, 229-233, 1992</Citation>
-<Title>Primary structure of the Aequorea victoria green-fluorescent protein.</Title>
-<Xref>DOI:10.1016/0378-1119(92)90691-H</Xref>
-<Xref>PMID:1347277</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yang, F.</Author>
-<Author>Moss, L.G.</Author>
-<Author>Phillips Jr., G.N.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, August 1996</Citation>
-<Description>Structure of green fluorescent protein.</Description>
-<Xref>PDB:1GFL</Xref>
-<Note>X-ray diffraction, 1.9 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yang, F.</Author>
-<Author>Moss, L.G.</Author>
-<Author>Phillips Jr., G.N.</Author>
-</Authors>
-<Citation>Nature Biotechnol. 14, 1246-1251, 1996</Citation>
-<Title>The molecular structure of green fluorescent protein.</Title>
-<Xref>DOI:10.1038/nbt1096-1246</Xref>
-<Xref>PMID:9631087</Xref>
-<Note>X-ray diffraction, 1.9 angstroms</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>Y</SequenceSpec>
-<Condition>incidental to RESID:AA0184</Condition>
-<Condition>incidental to RESID:AA0187</Condition>
-<Condition>incidental to RESID:AA0188</Condition>
-<Condition>incidental to RESID:AA0189</Condition>
-<Condition>incidental to RESID:AA0378</Condition>
-<Condition>incidental to RESID:AA0379</Condition>
-<Condition>incidental to RESID:AA0380</Condition>
-<Condition>incidental to RESID:AA0381</Condition>
-<Xref>GO:0018251</Xref>
-<Xref>GO:0030921</Xref>
-<Xref>PSI-MOD:00191</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="mod_res__(z)-2,3-didehydrotyrosine__y">MOD_RES (Z)-2,3-didehydrotyrosine</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="mod_res__2,3-didehydrotyrosine__y">MOD_RES 2,3-didehydrotyrosine</Feature>
-<Note>this UniProt feature is used when the isomeric structure has not been determined</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0183.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0183.PDB" />
-</Entry>
-<Entry id="AA0184">
-<Header>
-<Code>AA0184</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>02-Nov-1999</StrucRevDate>
-<TextChngDate>13-Sep-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-serine 5-imidazolinone glycine</Name>
-<AlternateName>2-[1-amino-2-hydroxyethyl]-1-carboxymethyl-1-imidazolin-5-one</AlternateName>
-<AlternateName>4-methylidene-imidazole-5-one (MIO) active site</AlternateName>
-<AlternateName>green fluorescent protein chromophore</AlternateName>
-<AlternateName>para-hydroxybenzylidene-imidazolidinone chromophore</AlternateName>
-<AlternateName>seryl-5-imidazolinone glycine</AlternateName>
-<SystematicName>(2-[(1R)-1-amino-2-hydroxyethyl]-5-oxo-4,5-dihydro-1H-imidazol-1-yl)acetic acid</SystematicName>
-<Xref>PDBHET:GYS</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 6 N 2 O 2</Formula>
-<Weight type="chemical">126.11</Weight>
-<Weight type="physical">126.042927</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016 AA0008">
-<Formula>C 0 H -2 N 0 O -1</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Prasher, D.C.</Author>
-<Author>Eckenrode, V.K.</Author>
-<Author>Ward, W.W.</Author>
-<Author>Prendergast, F.G.</Author>
-<Author>Cormier, M.J.</Author>
-</Authors>
-<Citation>Gene 111, 229-233, 1992</Citation>
-<Title>Primary structure of the Aequorea victoria green-fluorescent protein.</Title>
-<Xref>DOI:10.1016/0378-1119(92)90691-H</Xref>
-<Xref>PMID:1347277</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yang, F.</Author>
-<Author>Moss, L.G.</Author>
-<Author>Phillips Jr., G.N.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, August 1996</Citation>
-<Description>Structure of green fluorescent protein.</Description>
-<Xref>PDB:1GFL</Xref>
-<Note>X-ray diffraction, 1.9 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yang, F.</Author>
-<Author>Moss, L.G.</Author>
-<Author>Phillips Jr., G.N.</Author>
-</Authors>
-<Citation>Nature Biotechnol. 14, 1246-1251, 1996</Citation>
-<Title>The molecular structure of green fluorescent protein.</Title>
-<Xref>DOI:10.1038/nbt1096-1246</Xref>
-<Xref>PMID:9631087</Xref>
-<Note>X-ray diffraction, 1.9 angstroms</Note>
-</ReferenceBlock>
-<Comment>This entry represents the cross-link of the peptide backbone from the alpha-carboxyl carbon of residue N, a serine, to the alpha-amino nitrogen of residue N+2, a glycine, coupled with the formation of a double bond to the alpha-amino nitrogen of residue N+1 which loses one hydrogen, and the loss of a molecule of water.</Comment>
-<Comment>This cross-link is accompanied by modification of residue N+1. The modified residue N+1 is presented in a separate entry and is not included in the mass accounting of this entry. The backbone atoms of residue N+1 are shown in gray in the diagram.</Comment>
-<Comment>The chirality of residue N is (R) rather then (S) because of the reversed order of precedence with respect to the beta-carbon methoxy group of the 5-imidazolinone group replacing the carboxyl group.</Comment>
-<Comment>The modification of serine to dehydroalanine coupled with the formation of 5-imidazolinone by the two neighboring residues produces the 4-methylidene-imidazole-5-one (MIO) active site of some amino acid ammonia-lyases that differs by UV and mass spectrometric evidence from other known dehydroalanine containing peptides not containing the second modification.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>G, S</SequenceSpec>
-<Condition>carboxamidine</Condition>
-<Condition>cross-link 1</Condition>
-<Condition>incidental to RESID:AA0183</Condition>
-<Condition>incidental to RESID:AA0365</Condition>
-<Xref>GO:0018252</Xref>
-<Xref>GO:0018253</Xref>
-<Xref>PSI-MOD:00192</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chromoprotein</Keyword>
-<Keyword>imidazolinone/oxazolinone ring</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__5-imidazolinone (ser-gly)__s__g">CROSSLNK 5-imidazolinone (Ser-Gly)</Feature>
-</Features>
-<Image src="/images/AA0184.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0184.PDB" />
-</Entry>
-<Entry id="AA0185">
-<Header>
-<Code>AA0185</Code>
-<Dates>
-<CreationDate>26-Oct-1995</CreationDate>
-<StrucRevDate>26-Oct-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-3-oxoalanine</Name>
-<AlternateName>2-amino-3-oxopropionic acid</AlternateName>
-<AlternateName>C(alpha)-formylglycine [misnomer]</AlternateName>
-<AlternateName>L-amino-malonic acid semialdehyde</AlternateName>
-<AlternateName>L-aminomalonaldehydic acid</AlternateName>
-<AlternateName>L-serinesemialdehyde [misnomer]</AlternateName>
-<SystematicName>(S)-2-amino-3-oxopropanoic acid</SystematicName>
-<Xref>CAS:5735-66-0</Xref>
-<Xref>ChEBI:85621</Xref>
-<Xref>PDBHET:FGL</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 3 N 1 O 2</Formula>
-<Weight type="chemical">85.06</Weight>
-<Weight type="physical">85.016378</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005" label="CYS">
-<Formula>C 0 H -2 N 0 O 1 S -1</Formula>
-<Weight type="chemical">-18.08</Weight>
-<Weight type="physical">-17.992806</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0016" label="SER">
-<Formula>C 0 H -2 N 0 O 0</Formula>
-<Weight type="chemical">-2.02</Weight>
-<Weight type="physical">-2.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Schmidt, B.</Author>
-<Author>Selmer, T.</Author>
-<Author>Ingendoh, A.</Author>
-<Author>von Figura, K.</Author>
-</Authors>
-<Citation>Cell 82, 271-278, 1995</Citation>
-<Title>A novel amino acid modification in sulfatases that is defective in multiple sulfatase deficiency.</Title>
-<Xref>DOI:10.1016/0092-8674(95)90314-3</Xref>
-<Xref>PMID:7628016</Xref>
-<Note>mass spectrometric detection</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Selmer, T.</Author>
-<Author>Hallmann, A.</Author>
-<Author>Schmidt, B.</Author>
-<Author>Sumper, M.</Author>
-<Author>von Figura, K.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 238, 341-345, 1996</Citation>
-<Title>The evolutionary conservation of a novel protein modification, the conversion of cysteine to serinesemialdehyde in arylsulfatase from Volvox carteri.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1996.0341z.x</Xref>
-<Xref>PMID:8681943</Xref>
-<Note>mass spectrometric and chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Miech, C.</Author>
-<Author>Dierks, T.</Author>
-<Author>Selmer, T.</Author>
-<Author>von Figura, K.</Author>
-<Author>Schmidt, B.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 273, 4835-4837, 1998</Citation>
-<Title>Arylsulfatase from Klebsiella pneumoniae carries a formylglycine generated from a serine.</Title>
-<Xref>DOI:10.1074/jbc.273.9.4835</Xref>
-<Xref>PMID:9478923</Xref>
-<Note>mass spectrometric and chemical characterization; radioisotope labeling; modification of serine is demonstrated</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Landgrebe, J.</Author>
-<Author>Dierks, T.</Author>
-<Author>Schmidt, B.</Author>
-<Author>von Figura, K.</Author>
-</Authors>
-<Citation>Gene 316, 47-56, 2003</Citation>
-<Title>The human SUMF1 gene, required for posttranslational sulfatase modification, defines a new gene family which is conserved from pro- to eukaryotes.</Title>
-<Xref>DOI:10.1016/S0378-1119(03)00746-7</Xref>
-<Xref>PMID:14563551</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Peng, J.</Author>
-<Author>Schmidt, B.</Author>
-<Author>von Figura, K.</Author>
-<Author>Dierks, T.</Author>
-</Authors>
-<Citation>J. Mass Spectrom. 38, 80-86, 2003</Citation>
-<Title>Identification of formylglycine in sulfatases by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.</Title>
-<Xref>DOI:10.1002/jms.404</Xref>
-<Xref>PMID:12526009</Xref>
-<Note>mass spectrometric detection</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Benjdia, A.</Author>
-<Author>Subramanian, S.</Author>
-<Author>Leprince, J.</Author>
-<Author>Vaudry, H.</Author>
-<Author>Johnson, M.K.</Author>
-<Author>Berteau, O.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 283, 17815-17826, 2008</Citation>
-<Title>Anaerobic sulfatase-maturating enzymes, first dual substrate radical S-adenosylmethionine enzymes.</Title>
-<Xref>DOI:10.1074/jbc.M710074200</Xref>
-<Xref>PMID:18408004</Xref>
-<Note>one bacterial "radical-SAM" enzyme uses S-adenosylmethionine to convert both serine and cysteine at sulfatase active sites</Note>
-</ReferenceBlock>
-<Comment>The modified cysteine is found in sulfatases at the second position in the sequence motif [L/V]C[A/C/S/T]PSR.</Comment>
-<Comment>In at least one case, the oxidation acceptor or cofactor for the generating enzyme is known to be S-adenosylmethionine. The generating enzyme activity acting on serine would be EC 1.1.99.-, and acting on cysteine would be EC 1.8.99.-.</Comment>
-<Comment>This modification should not be confused with N-formylglycine (see RESID:AA0057). The use of the misleading, non-standard name "C-alpha-formyl glycine" should be avoided.</Comment>
-<Comment>This active site residue occurs in the hydrated form, 2-amino-3,3-dihydroxypropanoic acid, as observed in crystallographic structures.  See RESID:AA0492.</Comment>
-<Comment>The PDB Hetgroup FGL was originally designated as the "C(alpha)-formyl glycine" active site residue L-3-oxoalanine observed in its hydrated form. That structure, a gem-diol with an sp(3) carbon, was misinterpreted as a carboxyl with an sp(2) carbon, and assigned to aminomalonic acid (see RESID:AA0458) instead.</Comment>
-<GeneratingEnzyme>
-<EnzymeName link="SER">sulfatase maturing enzyme (sulfatase modifying factor, C-alpha-formylglycine-generating enzyme) (EC 1.1.99.-)</EnzymeName>
-<EnzymeName link="CYS">sulfatase maturing enzyme (sulfatase modifying factor, C-alpha-formylglycine-generating enzyme) (EC 1.8.99.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode link="CYS">
-<SequenceSpec>C</SequenceSpec>
-<Xref>GO:0018083</Xref>
-<Xref>PSI-MOD:00193</Xref>
-<Xref>PSI-MOD:01169</Xref>
-</SequenceCode>
-<SequenceCode link="SER">
-<SequenceSpec>S</SequenceSpec>
-<Xref>GO:0018083</Xref>
-<Xref>PSI-MOD:00835</Xref>
-<Xref>PSI-MOD:01169</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="mod_res__3-oxoalanine (cys)__c" link="CYS">MOD_RES 3-oxoalanine (Cys)</Feature>
-<Feature type="UniProt" key="mod_res__3-oxoalanine (ser)__s" link="SER">MOD_RES 3-oxoalanine (Ser)</Feature>
-</Features>
-<Image src="/images/AA0185.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0185.PDB" />
-</Entry>
-<Entry id="AA0186">
-<Header>
-<Code>AA0186</Code>
-<Dates>
-<CreationDate>23-Jan-1998</CreationDate>
-<StrucRevDate>31-Dec-2011</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>lactic acid</Name>
-<AlternateName>2-hydroxypropionic acid</AlternateName>
-<AlternateName>alpha-hydroxypropionic acid</AlternateName>
-<SystematicName>(2R)-2-hydroxypropanoic acid</SystematicName>
-<Xref>CAS:10326-41-7</Xref>
-<Xref>ChEBI:42111</Xref>
-<Xref>PDBHET:LAC</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 5 O 2</Formula>
-<Weight type="chemical">73.07</Weight>
-<Weight type="physical">73.028954</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 0 H -1 N -1 O 0</Formula>
-<Weight type="chemical">-15.02</Weight>
-<Weight type="physical">-15.010899</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>van de Kamp, M.</Author>
-<Author>van den Hooven, H.W.</Author>
-<Author>Konings, R.N.H.</Author>
-<Author>Bierbaum, G.</Author>
-<Author>Sahl, H.G.</Author>
-<Author>Kuipers, O.P.</Author>
-<Author>Siezen, R.J.</Author>
-<Author>de Vos, W.M.</Author>
-<Author>Hilbers, C.W.</Author>
-<Author>van de Ven, F.J.M.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 230, 587-600, 1995</Citation>
-<Title>Elucidation of the primary structure of the lantibiotic epilancin K7 from Staphylococcus epidermidis K7. Cloning and characterisation of the epilancin-K7-encoding gene and NMR analysis of mature epilancin K7.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1995.tb20600.x</Xref>
-<Xref>PMID:7607233</Xref>
-<Note>(1)H-NMR and (13)C-NMR identification; the stereochemistry was not determined</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Velásquez, J.E.</Author>
-<Author>Zhang, X.</Author>
-<Author>van der Donk, W.A.</Author>
-</Authors>
-<Citation>Chem. Biol. 18, 857-867, 2011</Citation>
-<Title>Biosynthesis of the antimicrobial peptide epilancin 15X and its N-terminal lactate.</Title>
-<Xref>DOI:10.1016/j.chembiol.2011.05.007</Xref>
-<Xref>PMID:21802007</Xref>
-<Note>the lactoyl group of epilancin 15X is shown to be the D- stereoisomer by enzymatic analysis</Note>
-</ReferenceBlock>
-<Comment>The stereochemistry has not been determined in all the peptides with this modification.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>protein-serine dehydratase ElxB (EC 4.2.1.-)</EnzymeName>
-<EnzymeName>D-lactoyl-protein dehydrogenase ElxO (EC 1.1.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0018084</Xref>
-<Xref>PSI-MOD:00194</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__lactic acid__s">MOD_RES Lactic acid</Feature>
-</Features>
-<Image src="/images/AA0186.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0186.PDB" />
-</Entry>
-<Entry id="AA0187">
-<Header>
-<Code>AA0187</Code>
-<Dates>
-<CreationDate>14-May-1999</CreationDate>
-<StrucRevDate>02-Nov-2001</StrucRevDate>
-<TextChngDate>30-Sep-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-alanine 5-imidazolinone glycine</Name>
-<AlternateName>2-[1-aminoethyl]-1-carboxymethyl-1-imidazolin-5-one</AlternateName>
-<AlternateName>4-methylidene-imidazole-5-one active site</AlternateName>
-<AlternateName>alanyl-5-imidazolinone glycine</AlternateName>
-<AlternateName>para-hydroxybenzylidene-imidazolidinone chromophore</AlternateName>
-<SystematicName>(2-[(1S)-1-aminoethyl]-5-oxo-4,5-dihydro-1H-imidazol-1-yl)acetic acid</SystematicName>
-<Xref>PDBHET:AYG</Xref>
-<Xref>PDBHET:MDO</Xref>
-<Xref>PDBHET:X9Q</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 6 N 2 O 1</Formula>
-<Weight type="chemical">110.12</Weight>
-<Weight type="physical">110.048013</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0001 AA0008">
-<Formula>C 0 H -2 N 0 O -1</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Schwede, T.F.</Author>
-<Author>Retey, J.</Author>
-<Author>Schulz, G.E.</Author>
-</Authors>
-<Citation>Biochemistry 38, 5355-5361, 1999</Citation>
-<Title>Crystal structure of histidine ammonia-lyase revealing a novel polypeptide modification as the catalytic electrophile.</Title>
-<Xref>DOI:10.1021/bi982929q</Xref>
-<Xref>PMID:10220322</Xref>
-<Note>X-ray diffraction, 2.1 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Baedeker, M.</Author>
-<Author>Schulz, G.E.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 269, 1790-1797, 2002</Citation>
-<Title>Structures of two histidine ammonia-lyase modifications and implications for the catalytic mechanism.</Title>
-<Xref>DOI:10.1046/j.1432-1327.2002.02827.x</Xref>
-<Xref>PMID:11895450</Xref>
-<Note>X-ray diffraction, 1.7 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Baedeker, M.</Author>
-<Author>Schulz, G.E.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, August 2001</Citation>
-<Description>Histidine ammonia-lyase (HAL) from Pseudomonas putida inhibited with L-cysteine.</Description>
-<Xref>PDB:1GKM</Xref>
-<Note>X-ray diffraction, 1.00 angstroms</Note>
-</ReferenceBlock>
-<Comment>This entry represents the cross-link of the peptide backbone from the alpha-carboxyl carbon of residue N, an alanine, to the alpha-amino nitrogen of residue N+2, a glycine, coupled with the formation of a double bond to the alpha-amino nitrogen of residue N+1 which loses one hydrogen, and the loss of a molecule of water.</Comment>
-<Comment>This cross-link is accompanied by modification of residue N+1. The modified residue N+1 is presented in a separate entry and is not included in the mass accounting of this entry. The backbone atoms of residue N+1 are shown in gray in the diagram.</Comment>
-<SequenceCode>
-<SequenceSpec>A, G</SequenceSpec>
-<Condition>carboxamidine</Condition>
-<Condition>cross-link 1</Condition>
-<Condition>incidental to RESID:AA0181</Condition>
-<Condition>incidental to RESID:AA0183</Condition>
-<Condition>incidental to RESID:AA0365</Condition>
-<Xref>GO:0018253</Xref>
-<Xref>GO:0018313</Xref>
-<Xref>PSI-MOD:00195</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chromoprotein</Keyword>
-<Keyword>imidazolinone/oxazolinone ring</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__5-imidazolinone (ala-gly)__a__g">CROSSLNK 5-imidazolinone (Ala-Gly)</Feature>
-</Features>
-<Image src="/images/AA0187.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0187.PDB" />
-</Entry>
-<Entry id="AA0188">
-<Header>
-<Code>AA0188</Code>
-<Dates>
-<CreationDate>24-Nov-1999</CreationDate>
-<StrucRevDate>24-Nov-1999</StrucRevDate>
-<TextChngDate>13-Sep-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-cysteine 5-imidazolinone glycine</Name>
-<AlternateName>2-[1-amino-2-sulfanylethyl]-1-carboxymethyl-1-imidazolin-5-one</AlternateName>
-<AlternateName>4-methylidene-imidazole-5-one (MIO) active site</AlternateName>
-<AlternateName>cysteinyl-5-imidazolinone glycine</AlternateName>
-<AlternateName>para-hydroxybenzylidene-imidazolidinone chromophore</AlternateName>
-<SystematicName>(2-[(1R)-1-amino-2-sulfanylethyl]-5-oxo-4,5-dihydro-1H-imidazol-1-yl)acetic acid</SystematicName>
-<Xref>PDBHET:GYC</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 6 N 2 O 1 S 1</Formula>
-<Weight type="chemical">142.18</Weight>
-<Weight type="physical">142.020084</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0008">
-<Formula>C 0 H -2 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wu, P.C.</Author>
-<Author>Kroening, T.A.</Author>
-<Author>White, P.J.</Author>
-<Author>Kendrick, K.E.</Author>
-</Authors>
-<Citation>J. Bacteriol. 174, 1647-1655, 1992</Citation>
-<Title>Purification of histidase from Streptomyces griseus and nucleotide sequence of the hutH structural gene.</Title>
-<Xref>PMID:1537807</Xref>
-<Note>prediction of dehydroalanine active site</Note>
-</ReferenceBlock>
-<Comment>This entry represents the cross-link of the peptide backbone from the alpha-carboxyl carbon of residue N, a cysteine, to the alpha-amino nitrogen of residue N+2, a glycine, coupled with the formation of a double bond to the alpha-amino nitrogen of residue N+1 which loses one hydrogen, and the loss of a molecule of water.</Comment>
-<Comment>This cross-link is accompanied by modification of residue N+1.</Comment>
-<Comment>The modification of serine to dehydroalanine coupled with the formation of 5-imidazolinone by the two neighboring residues produces the 4-methylidene-imidazole-5-one (MIO) active site of some amino acid ammonia-lyases that differs by UV and mass spectrometric evidence from other known dehydroalanine containing peptides not containing the second modification.</Comment>
-<SequenceCode>
-<SequenceSpec>C, G</SequenceSpec>
-<Condition>carboxamidine</Condition>
-<Condition>cross-link 1</Condition>
-<Condition>incidental to RESID:AA0181</Condition>
-<Condition>incidental to RESID:AA0183</Condition>
-<Condition>incidental to RESID:AA0365</Condition>
-<Xref>GO:0018253</Xref>
-<Xref>GO:0050745</Xref>
-<Xref>PSI-MOD:00196</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chromoprotein</Keyword>
-<Keyword>imidazolinone/oxazolinone ring</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__5-imidazolinone (cys-gly)__c__g">CROSSLNK 5-imidazolinone (Cys-Gly)</Feature>
-</Features>
-<Image src="/images/AA0188.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0188.PDB" />
-</Entry>
-<Entry id="AA0189">
-<Header>
-<Code>AA0189</Code>
-<Dates>
-<CreationDate>02-Nov-2001</CreationDate>
-<StrucRevDate>02-Nov-2001</StrucRevDate>
-<TextChngDate>20-May-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>2-imino-glutamine 5-imidazolinone glycine</Name>
-<AlternateName>2,N-didehydroglutaminyl-5-imidazolinone glycine</AlternateName>
-<AlternateName>2-(3-carbamoyl-1-imino-propyl)-1-carboxymethyl-1-imidazolin-5-one</AlternateName>
-<AlternateName>fluorescent protein FP583 chromophore</AlternateName>
-<AlternateName>para-hydroxybenzylidene-imidazolidinone chromophore</AlternateName>
-<AlternateName>red fluorescent protein chromophore</AlternateName>
-<AlternateName>[2-(3-carbamoyl-1-imino-propyl)-5-oxo-4,5-dihydro-imidazol-1-yl]-acetic acid</AlternateName>
-<SystematicName>[2-(4-amino-4-oxobutanimidoyl)-5-oxo-4,5-dihydro-1H-imidazol-1-yl]acetic acid</SystematicName>
-<Xref>PDBHET:CRQ</Xref>
-<Xref>PDBHET:QLG</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 7 N 3 O 2</Formula>
-<Weight type="chemical">165.15</Weight>
-<Weight type="physical">165.053826</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0007 AA0008">
-<Formula>C 0 H -4 N 0 O -1</Formula>
-<Weight type="chemical">-20.03</Weight>
-<Weight type="physical">-20.026215</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gross, L.A.</Author>
-<Author>Baird, G.S.</Author>
-<Author>Hoffman, R.C.</Author>
-<Author>Baldridge, K.K.</Author>
-<Author>Tsien, R.Y.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 97, 11990-11995, 2000</Citation>
-<Title>The structure of the chromophore within DsRed, a red fluorescent protein from coral.</Title>
-<Xref>DOI:10.1073/pnas.97.22.11990</Xref>
-<Xref>PMID:11050230</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yarbrough, D.</Author>
-<Author>Wachter, R.M.</Author>
-<Author>Kallio, K.</Author>
-<Author>Matz, M.V.</Author>
-<Author>Remington, S.J.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, December 2000</Citation>
-<Description>Crystal structure of DsRed, a red fluorescent protein from Discosoma sp. red.</Description>
-<Xref>PDB:1G7K</Xref>
-<Note>X-ray diffraction, 2.00 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yarbrough, D.</Author>
-<Author>Wachter, R.M.</Author>
-<Author>Kallio, K.</Author>
-<Author>Matz, M.V.</Author>
-<Author>Remington, S.J.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 98, 462-467, 2001</Citation>
-<Title>Refined crystal structure of DsRed, a red fluorescent protein from coral, at 2.0-A resolution.</Title>
-<Xref>DOI:10.1073/pnas.98.2.462</Xref>
-<Xref>PMID:11209050</Xref>
-</ReferenceBlock>
-<Comment>This entry represents the cross-link of the peptide backbone from the alpha-carboxyl carbon of residue N, a glutamine, to the alpha-amino nitrogen of residue N+2, a glycine, coupled with the formation of a double bond to the alpha-amino nitrogen of residue N, and the loss of a molecule of water.</Comment>
-<Comment>This cross-link is accompanied by modification of residue N+1. The modified residue N+1 is presented in a separate entry and is not included in the mass accounting of this entry. The backbone atoms of residue N+1 are shown in gray in the diagram.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>G, Q</SequenceSpec>
-<Condition>carboxamidine</Condition>
-<Condition>cross-link 1</Condition>
-<Condition>incidental to RESID:AA0183</Condition>
-<Condition>incidental to RESID:AA0365</Condition>
-<Xref>GO:0019729</Xref>
-<Xref>PSI-MOD:00197</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chromoprotein</Keyword>
-<Keyword>imidazolinone/oxazolinone ring</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__2-iminomethyl-5-imidazolinone (gln-gly)__q__g">CROSSLNK 2-iminomethyl-5-imidazolinone (Gln-Gly)</Feature>
-</Features>
-<Image src="/images/AA0189.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0189.PDB" />
-</Entry>
-<Entry id="AA0190">
-<Header>
-<Code>AA0190</Code>
-<Dates>
-<CreationDate>30-Jun-2012</CreationDate>
-<StrucRevDate>30-Jun-2012</StrucRevDate>
-<TextChngDate>30-Jun-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>D-aspartic acid</Name>
-<AlternateName>2-azanylbutanedioic acid</AlternateName>
-<AlternateName>aminosuccinic acid</AlternateName>
-<SystematicName>(2R)-2-aminobutanedioic acid</SystematicName>
-<Xref>CAS:1783-96-6</Xref>
-<Xref>ChEBI:48094</Xref>
-<Xref>PDBHET:DAS</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 5 N 1 O 3</Formula>
-<Weight type="chemical">115.09</Weight>
-<Weight type="physical">115.026943</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0004" label="ASP">
-<Formula>C 0 H 0 N 0 O 0</Formula>
-<Weight type="chemical">0.00</Weight>
-<Weight type="physical">0.000000</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0003" label="ASN">
-<Formula>C 0 H -1 N -1 O 1</Formula>
-<Weight type="chemical">0.98</Weight>
-<Weight type="physical">0.984016</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Di Marco, S.</Author>
-<Author>Priestle, J.P.</Author>
-</Authors>
-<Citation>Structure 5, 1465-1474, 1997</Citation>
-<Title>Structure of the complex of leech-derived tryptase inhibitor (LDTI) with trypsin and modeling of the LDTI-tryptase system.</Title>
-<Xref>PMID:9384562</Xref>
-<Note>X-ray diffraction, 2.03 angstroms; porcine trypsin in complex with leech-derived tryptase inhibitor can apparently crystallize only after the spontaneous conversion of Asn-115 to D-Asp via a succinimde intermediate</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Di Marco, S.</Author>
-<Author>Priestle, J.P.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, June 1997</Citation>
-<Description>Leech-derived tryptase inhibitor/trypsin complex.</Description>
-<Xref>PDB:1AN1</Xref>
-<Note>X-ray diffraction, 2.03 angstroms</Note>
-</ReferenceBlock>
-<Comment>The stereoisomeric conversion of L-aspartic acid or L-asparagine to D-aspartic acid is probably mediated by the spontaneous cyclization and deamidation to a 2-aminosuccinimidyl group (see RESID:AA0441).</Comment>
-<SequenceCode link="ASP">
-<SequenceSpec>D</SequenceSpec>
-<Xref>PSI-MOD:01921</Xref>
-</SequenceCode>
-<SequenceCode link="ASN">
-<SequenceSpec>N</SequenceSpec>
-<Xref>PSI-MOD:01930</Xref>
-</SequenceCode>
-<Source>artifactual</Source>
-<Keywords>
-<Keyword>D-amino acid</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0190.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0190.PDB" />
-</Entry>
-<Entry id="AA0191">
-<Header>
-<Code>AA0191</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>25-Feb-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>D-alanine</Name>
-<SystematicName>(R)-2-aminopropanoic acid</SystematicName>
-<Xref>CAS:338-69-2</Xref>
-<Xref>ChEBI:29949</Xref>
-<Xref>PDBHET:DAL</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 5 N 1 O 1</Formula>
-<Weight type="chemical">71.08</Weight>
-<Weight type="physical">71.037114</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0001" label="ALA">
-<Formula>C 0 H 0 N 0 O 0</Formula>
-<Weight type="chemical">0.00</Weight>
-<Weight type="physical">0.000000</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0016" label="SER">
-<Formula>C 0 H 0 N 0 O -1</Formula>
-<Weight type="chemical">-16.00</Weight>
-<Weight type="physical">-15.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Montecucchi, P.C.</Author>
-<Author>de Castiglione, R.</Author>
-<Author>Erspamer, V.</Author>
-</Authors>
-<Citation>Int. J. Pept. Protein Res. 17, 316-321, 1981</Citation>
-<Title>Identification of dermorphin and Hyp(6)-dermorphin in skin extracts of the Brazilian frog Phyllomedusa rhodei.</Title>
-<Xref>PMID:7287302</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Skaugen, M.</Author>
-<Author>Nissen-Meyer, J.</Author>
-<Author>Jung, G.</Author>
-<Author>Stevanovic, S.</Author>
-<Author>Sletten, K.</Author>
-<Author>Abildgaard, C.I.M.</Author>
-<Author>Nes, I.F.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 269, 27183-27185, 1994</Citation>
-<Title>In vivo conversion of L-serine to D-alanine in a ribosomally synthesized polypeptide.</Title>
-<Xref>PMID:7961627</Xref>
-<Note>the spelling of "C.I.M. Abildgaard" in the PubMed citation is corrected, and the name "C. Inger" is removed</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Martin, N.I.</Author>
-<Author>Sprules, T.</Author>
-<Author>Carpenter, M.R.</Author>
-<Author>Cotter, P.D.</Author>
-<Author>Hill, C.</Author>
-<Author>Ross, R.P.</Author>
-<Author>Vederas, J.C.</Author>
-</Authors>
-<Citation>Biochemistry 43, 3049-3056, 2004</Citation>
-<Title>Structural characterization of lacticin 3147, a two-peptide lantibiotic with synergistic activity.</Title>
-<Xref>DOI:10.1021/bi0362065</Xref>
-<Xref>PMID:15023056</Xref>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>protein-alanine epimerase (EC 5.1.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode link="ALA">
-<SequenceSpec>A</SequenceSpec>
-<Xref>GO:0019122</Xref>
-<Xref>GO:0019916</Xref>
-<Xref>PSI-MOD:00198</Xref>
-<Xref>PSI-MOD:00862</Xref>
-</SequenceCode>
-<SequenceCode link="SER">
-<SequenceSpec>S</SequenceSpec>
-<Xref>GO:0019122</Xref>
-<Xref>GO:0019917</Xref>
-<Xref>PSI-MOD:00858</Xref>
-<Xref>PSI-MOD:00862</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>D-amino acid</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__d-alanine (ala)__a" link="ALA">MOD_RES D-alanine (Ala)</Feature>
-<Feature type="UniProt" key="mod_res__d-alanine (ser)__s" link="SER">MOD_RES D-alanine (Ser)</Feature>
-</Features>
-<Image src="/images/AA0191.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0191.PDB" />
-</Entry>
-<Entry id="AA0192">
-<Header>
-<Code>AA0192</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>25-Feb-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>D-allo-isoleucine</Name>
-<AlternateName>2-azanyl-3-methylpentanoic acid</AlternateName>
-<AlternateName>3-methyl-norvaline</AlternateName>
-<AlternateName>allo-D-isoleucine</AlternateName>
-<AlternateName>alpha-amino-beta-methylvaleric acid</AlternateName>
-<AlternateName>D-threo-isoleucine</AlternateName>
-<SystematicName>(2R,3S)-2-amino-3-methylpentanoic acid</SystematicName>
-<Xref>CAS:1509-35-9</Xref>
-<Xref>ChEBI:30007</Xref>
-<Xref>PDBHET:DIL</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 11 N 1 O 1</Formula>
-<Weight type="chemical">113.16</Weight>
-<Weight type="physical">113.084064</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0010">
-<Formula>C 0 H 0 N 0 O 0</Formula>
-<Weight type="chemical">0.00</Weight>
-<Weight type="physical">0.000000</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mignogna, G.</Author>
-<Author>Simmaco, M.</Author>
-<Author>Kreil, G.</Author>
-<Author>Barra, D.</Author>
-</Authors>
-<Citation>EMBO J. 12, 4829-4832, 1993</Citation>
-<Title>Antibacterial and haemolytic peptides containing D-alloisoleucine from the skin of Bombina variegata.</Title>
-<Xref>PMID:8223491</Xref>
-<Note>chromatographic separation</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>protein-isoleucine 2-epimerase (EC 5.1.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>I</SequenceSpec>
-<Xref>GO:0019124</Xref>
-<Xref>PSI-MOD:00199</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>D-amino acid</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__d-allo-isoleucine__i">MOD_RES D-allo-isoleucine</Feature>
-</Features>
-<Image src="/images/AA0192.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0192.PDB" />
-</Entry>
-<Entry id="AA0193">
-<Header>
-<Code>AA0193</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>30-Sep-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>D-methionine</Name>
-<AlternateName>2-amino-4-(methylthio)butanoic acid</AlternateName>
-<AlternateName>2-amino-4-(methylthio)butyric acid</AlternateName>
-<SystematicName>(2R)-2-amino-4-(methylsulfanyl)butanoic acid</SystematicName>
-<Xref>CAS:348-67-4</Xref>
-<Xref>ChEBI:29984</Xref>
-<Xref>PDBHET:MED</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 9 N 1 O 1 S 1</Formula>
-<Weight type="chemical">131.19</Weight>
-<Weight type="physical">131.040485</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0013">
-<Formula>C 0 H 0 N 0 O 0 S 0</Formula>
-<Weight type="chemical">0.00</Weight>
-<Weight type="physical">0.000000</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kreil, G.</Author>
-<Author>Barra, D.</Author>
-<Author>Simmaco, M.</Author>
-<Author>Erspamer, V.</Author>
-<Author>Erspamer, G.F.</Author>
-<Author>Negri, L.</Author>
-<Author>Severini, C.</Author>
-<Author>Corsi, R.</Author>
-<Author>Melchiorri, P.</Author>
-</Authors>
-<Citation>Eur. J. Pharmacol. 162, 123-128, 1989</Citation>
-<Title>Deltorphin, a novel amphibian skin peptide with high selectivity and affinity for delta opioid receptors.</Title>
-<Xref>DOI:10.1016/0014-2999(89)90611-0</Xref>
-<Xref>PMID:2542051</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Torres, A.M.</Author>
-<Author>Tsampazi, C.</Author>
-<Author>Geraghty, D.P.</Author>
-<Author>Bansal, P.S.</Author>
-<Author>Alewood, P.F.</Author>
-<Author>Kuchel, P.W.</Author>
-</Authors>
-<Citation>Biochem. J. 391, 215-220, 2005</Citation>
-<Title>D-amino acid residue in a defensin-like peptide from platypus venom: effect on structure and chromatographic properties.</Title>
-<Xref>DOI:10.1042/BJ20050900</Xref>
-<Xref>PMID:16033333</Xref>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>protein-methionine epimerase (EC 5.1.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>M</SequenceSpec>
-<Xref>GO:0019123</Xref>
-<Xref>PSI-MOD:00200</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>D-amino acid</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__d-methionine__m">MOD_RES D-methionine</Feature>
-</Features>
-<Image src="/images/AA0193.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0193.PDB" />
-</Entry>
-<Entry id="AA0194">
-<Header>
-<Code>AA0194</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>20-May-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>D-phenylalanine</Name>
-<SystematicName>(R)-2-amino-3-phenylpropanoic acid</SystematicName>
-<Xref>CAS:673-06-3</Xref>
-<Xref>ChEBI:29996</Xref>
-<Xref>PDBHET:DPN</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 9 N 1 O 1</Formula>
-<Weight type="chemical">147.18</Weight>
-<Weight type="physical">147.068414</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0014">
-<Formula>C 0 H 0 N 0 O 0</Formula>
-<Weight type="chemical">0.00</Weight>
-<Weight type="physical">0.000000</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kamatani, Y.</Author>
-<Author>Minakata, H.</Author>
-<Author>Kenny, P.T.M.</Author>
-<Author>Iwashita, T.</Author>
-<Author>Watanabe, K.</Author>
-<Author>Funase, K.</Author>
-<Author>Sun, X.P.</Author>
-<Author>Yongsiri, A.</Author>
-<Author>Kim, K.H.</Author>
-<Author>Novales-Li, P.</Author>
-<Author>Novales, E.T.</Author>
-<Author>Kanapi, C.G.</Author>
-<Author>Takeuchi, H.</Author>
-<Author>Nomoto, K.</Author>
-</Authors>
-<Citation>Biochem. Biophys. Res. Commun. 160, 1015-1020, 1989</Citation>
-<Title>Achatin-I, an endogenous neuroexcitatory tetrapeptide from Achatina fulica Férussac containing a D-amino acid residue.</Title>
-<Xref>DOI:10.1016/S0006-291X(89)80103-2</Xref>
-<Xref>PMID:2597281</Xref>
-<Note>(1)H-NMR identification; chemical synthesis confirmation of stereochemistry; the truncated list of authors in the PubMed citation is corrected</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ishida, T.</Author>
-<Author>In, Y.</Author>
-<Author>Inoue, M.</Author>
-<Author>Yasuda-Kamatani, Y.</Author>
-<Author>Minakata, H.</Author>
-<Author>Iwashita, T.</Author>
-<Author>Nomoto, K.</Author>
-</Authors>
-<Citation>FEBS Lett. 307, 253-256, 1992</Citation>
-<Title>Effect of the D-Phe(2) residue on molecular conformation of an endogenous neuropeptide achatin-I. Comparison of X-ray crystal structures of achatin-I (H-Gly-D-Phe-Ala-Asp-OH) and achatin-II (H-Gly-Phe-Ala-Asp-OH).</Title>
-<Xref>DOI:10.1016/0014-5793(92)80689-E</Xref>
-<Xref>PMID:1644179</Xref>
-<Note>X-ray diffraction, 0.85 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Matsuyama, T.</Author>
-<Author>Kaneda, K.</Author>
-<Author>Nakagawa, Y.</Author>
-<Author>Isa, K.</Author>
-<Author>Hara-Hotta, H.</Author>
-<Author>Yano, I.</Author>
-</Authors>
-<Citation>J. Bacteriol. 174, 1769-1776, 1992</Citation>
-<Title>A novel extracellular cyclic lipopeptide which promotes flagellum-dependent and -independent spreading growth of Serratia marcescens.</Title>
-<Xref>PMID:1548227</Xref>
-<Note>mass spectrometric and (1)H-NMR characterization</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>protein-phenylalanine epimerase (EC 5.1.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>F</SequenceSpec>
-<Xref>GO:0019125</Xref>
-<Xref>PSI-MOD:00201</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>D-amino acid</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__d-phenylalanine__f">MOD_RES D-phenylalanine</Feature>
-</Features>
-<Image src="/images/AA0194.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0194.PDB" />
-</Entry>
-<Entry id="AA0195">
-<Header>
-<Code>AA0195</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>20-May-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>D-serine</Name>
-<SystematicName>(R)-2-amino-3-hydroxypropanoic acid</SystematicName>
-<Xref>CAS:312-84-5</Xref>
-<Xref>ChEBI:29998</Xref>
-<Xref>PDBHET:DSN</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 5 N 1 O 2</Formula>
-<Weight type="chemical">87.08</Weight>
-<Weight type="physical">87.032028</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016" label="SER">
-<Formula>C 0 H 0 N 0 O 0</Formula>
-<Weight type="chemical">0.00</Weight>
-<Weight type="physical">0.000000</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0005" label="CYS">
-<Formula>C 0 H 0 N 0 O 1 S -1</Formula>
-<Weight type="chemical">-16.06</Weight>
-<Weight type="physical">-15.977156</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Faulstich, H.</Author>
-<Author>Buku, A.</Author>
-<Author>Bodenmüller, H.</Author>
-<Author>Wieland, T.</Author>
-</Authors>
-<Citation>Biochemistry 19, 3334-3343, 1980</Citation>
-<Title>Virotoxins: actin-binding cyclic peptides of Amanita virosa mushrooms.</Title>
-<Xref>DOI:10.1021/bi00555a036</Xref>
-<Xref>PMID:6893271</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Heck, S.D.</Author>
-<Author>Siok, C.J.</Author>
-<Author>Krapcho, K.J.</Author>
-<Author>Kelbaugh, P.R.</Author>
-<Author>Thadeio, P.F.</Author>
-<Author>Welch, M.J.</Author>
-<Author>Williams, R.D.</Author>
-<Author>Ganong, A.H.</Author>
-<Author>Kelly, M.E.</Author>
-<Author>Lanzetti, A.J.</Author>
-<Author>Gray, W.R.</Author>
-<Author>Phillips, D.</Author>
-<Author>Parks, T.N.</Author>
-<Author>Jackson, H.</Author>
-<Author>Ahlijanian, M.K.</Author>
-<Author>Saccomano, N.A.</Author>
-<Author>Volkmann, R.A.</Author>
-</Authors>
-<Citation>Science 266, 1065-1068, 1994</Citation>
-<Title>Functional consequences of posttranslational isomerization of Ser(46) in a calcium channel toxin.</Title>
-<Xref>DOI:10.1126/science.7973665</Xref>
-<Xref>PMID:7973665</Xref>
-<Note>identification of enzymatically racemized serine; the truncated list of authors in the PubMed citation is corrected</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Shikata, Y.</Author>
-<Author>Watanabe, T.</Author>
-<Author>Teramoto, T.</Author>
-<Author>Inoue, A.</Author>
-<Author>Kawakami, Y.</Author>
-<Author>Nishizawa, Y.</Author>
-<Author>Katayama, K.</Author>
-<Author>Kuwada, M.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 270, 16719-16723, 1995</Citation>
-<Title>Isolation and characterization of a peptide isomerase from funnel web spider venom.</Title>
-<Xref>DOI:10.1074/jbc.270.28.16719</Xref>
-<Xref>PMID:7622482</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hallen, H.E.</Author>
-<Author>Luo, H.</Author>
-<Author>Scott-Craig, J.S.</Author>
-<Author>Walton, J.D.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 104, 19097-19101, 2007</Citation>
-<Title>Gene family encoding the major toxins of lethal Amanita mushrooms.</Title>
-<Xref>DOI:10.1073/pnas.0707340104</Xref>
-<Xref>PMID:18025465</Xref>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>protein-serine epimerase (EC 5.1.1.16)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode link="SER">
-<SequenceSpec>S</SequenceSpec>
-<Xref>GO:0019126</Xref>
-<Xref>PSI-MOD:00202</Xref>
-<Xref>PSI-MOD:00891</Xref>
-</SequenceCode>
-<SequenceCode link="CYS">
-<SequenceSpec>C</SequenceSpec>
-<Xref>PSI-MOD:00891</Xref>
-<Xref>PSI-MOD:00892</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>D-amino acid</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__d-serine (ser)__s" link="ser">MOD_RES D-serine (Ser)</Feature>
-<Feature type="UniProt" key="mod_res__d-serine (cys)__c" link="cys">MOD_RES D-serine (Cys)</Feature>
-</Features>
-<Image src="/images/AA0195.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0195.PDB" />
-</Entry>
-<Entry id="AA0196">
-<Header>
-<Code>AA0196</Code>
-<Dates>
-<CreationDate>30-Jun-1995</CreationDate>
-<StrucRevDate>22-Nov-1996</StrucRevDate>
-<TextChngDate>25-Feb-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>D-asparagine</Name>
-<AlternateName>D-alpha-aminosuccinamic acid</AlternateName>
-<AlternateName>D-aspartic acid beta-amide</AlternateName>
-<SystematicName>(R)-2-amino-4-butanediamic acid</SystematicName>
-<Xref>CAS:2058-58-4</Xref>
-<Xref>ChEBI:29957</Xref>
-<Xref>PDBHET:DSG</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 6 N 2 O 2</Formula>
-<Weight type="chemical">114.10</Weight>
-<Weight type="physical">114.042927</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0003">
-<Formula>C 0 H 0 N 0 O 0</Formula>
-<Weight type="chemical">0.00</Weight>
-<Weight type="physical">0.000000</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ohta, N.</Author>
-<Author>Kubota, I.</Author>
-<Author>Takao, T.</Author>
-<Author>Shimonishi, Y.</Author>
-<Author>Yasuda-Kamatani, Y.</Author>
-<Author>Minakata, H.</Author>
-<Author>Nomoto, K.</Author>
-<Author>Muneoka, Y.</Author>
-<Author>Kobayashi, M.</Author>
-</Authors>
-<Citation>Biochem. Biophys. Res. Commun. 178, 486-493, 1991</Citation>
-<Title>Fulicin, a novel neuropeptide containing a D-amino acid residue isolated from the ganglia of Achatina fulica.</Title>
-<Xref>DOI:10.1016/0006-291X(91)90133-R</Xref>
-<Xref>PMID:1859408</Xref>
-<Note>chromatographic spectrographic identification; stereochemical determination; chemical synthesis</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>protein-asparagine epimerase (EC 5.1.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>N</SequenceSpec>
-<Xref>GO:0018091</Xref>
-<Xref>PSI-MOD:00203</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>D-amino acid</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__d-asparagine__n">MOD_RES D-asparagine</Feature>
-</Features>
-<Image src="/images/AA0196.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0196.PDB" />
-</Entry>
-<Entry id="AA0197">
-<Header>
-<Code>AA0197</Code>
-<Dates>
-<CreationDate>22-Nov-1996</CreationDate>
-<StrucRevDate>22-Nov-1996</StrucRevDate>
-<TextChngDate>20-May-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>D-leucine</Name>
-<AlternateName>alpha-aminoisocaproic acid</AlternateName>
-<SystematicName>(2R)-2-amino-4-methylpentanoic acid</SystematicName>
-<Xref>CAS:328-38-1</Xref>
-<Xref>ChEBI:30005</Xref>
-<Xref>PDBHET:DLE</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 11 N 1 O 1</Formula>
-<Weight type="chemical">113.16</Weight>
-<Weight type="physical">113.084064</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0011">
-<Formula>C 0 H 0 N 0 O 0</Formula>
-<Weight type="chemical">0.00</Weight>
-<Weight type="physical">0.000000</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fujisawa, Y.</Author>
-<Author>Ikeda, T.</Author>
-<Author>Nomoto, K.</Author>
-<Author>Yasuda-Kamatani, Y.</Author>
-<Author>Minakata, H.</Author>
-<Author>Kenny, P.T.M.</Author>
-<Author>Kubota, I.</Author>
-<Author>Muneoka, Y.</Author>
-</Authors>
-<Citation>Comp. Biochem. Physiol. C, Comp. Pharmacol. Toxicol. 102, 91-95, 1992</Citation>
-<Title>The FMRFamide-related decapeptide of Mytilus contains a D-amino acid residue.</Title>
-<Xref>DOI:10.1016/0742-8413(92)90049-D</Xref>
-<Xref>PMID:1358533</Xref>
-<Note>chromatographic detection; chemical synthesis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Matsuyama, T.</Author>
-<Author>Kaneda, K.</Author>
-<Author>Nakagawa, Y.</Author>
-<Author>Isa, K.</Author>
-<Author>Hara-Hotta, H.</Author>
-<Author>Yano, I.</Author>
-</Authors>
-<Citation>J. Bacteriol. 174, 1769-1776, 1992</Citation>
-<Title>A novel extracellular cyclic lipopeptide which promotes flagellum-dependent and -independent spreading growth of Serratia marcescens.</Title>
-<Xref>PMID:1548227</Xref>
-<Note>mass spectrometric and (1)H-NMR characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Jacobsen, R.B.</Author>
-<Author>Jimenez, E.C.</Author>
-<Author>De la Cruz, R.G.</Author>
-<Author>Gray, W.R.</Author>
-<Author>Cruz, L.J.</Author>
-<Author>Olivera, B.M.</Author>
-</Authors>
-<Citation>J. Pept. Res. 54, 93-99, 1999</Citation>
-<Title>A novel D-leucine-containing Conus peptide: diverse conformational dynamics in the contryphan family.</Title>
-<Xref>DOI:10.1034/j.1399-3011.1999.00093.x</Xref>
-<Xref>PMID:10461743</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Torres, A.M.</Author>
-<Author>Menz, I.</Author>
-<Author>Alewood, P.F.</Author>
-<Author>Bansal, P.</Author>
-<Author>Lahnstein, J.</Author>
-<Author>Gallagher, C.H.</Author>
-<Author>Kuchel, P.W.</Author>
-</Authors>
-<Citation>FEBS Lett. 524, 172-176, 2002</Citation>
-<Title>D-Amino acid residue in the C-type natriuretic peptide from the venom of the mammal, Ornithorhynchus anatinus, the Australian platypus.</Title>
-<Xref>DOI:10.1016/S0014-5793(02)03050-8</Xref>
-<Xref>PMID:12135762</Xref>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>protein-leucine epimerase (EC 5.1.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>L</SequenceSpec>
-<Xref>GO:0019129</Xref>
-<Xref>PSI-MOD:00204</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>D-amino acid</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__d-leucine__l">MOD_RES D-leucine</Feature>
-</Features>
-<Image src="/images/AA0197.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0197.PDB" />
-</Entry>
-<Entry id="AA0198">
-<Header>
-<Code>AA0198</Code>
-<Dates>
-<CreationDate>22-Nov-1996</CreationDate>
-<StrucRevDate>22-Nov-1996</StrucRevDate>
-<TextChngDate>31-Mar-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>D-tryptophan</Name>
-<AlternateName>alpha-amino-beta-(3-indolyl)propionoic acid</AlternateName>
-<SystematicName>(R)-2-amino-3-(1H-indol-3-yl)propanoic acid</SystematicName>
-<Xref>CAS:153-94-6</Xref>
-<Xref>ChEBI:29955</Xref>
-<Xref>PDBHET:DTR</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 11 H 10 N 2 O 1</Formula>
-<Weight type="chemical">186.21</Weight>
-<Weight type="physical">186.079313</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0018">
-<Formula>C 0 H 0 N 0 O 0</Formula>
-<Weight type="chemical">0.00</Weight>
-<Weight type="physical">0.000000</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Jimenez, E.C.</Author>
-<Author>Olivera, B.M.</Author>
-<Author>Gray, W.R.</Author>
-<Author>Cruz, L.J.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 271, 28002-28005, 1996</Citation>
-<Title>Contryphan is a D-tryptophan-containing Conus peptide.</Title>
-<Xref>DOI:10.1074/jbc.271.45.28002</Xref>
-<Xref>PMID:8910408</Xref>
-<Note>chromatographic detection; chemical synthesis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yano, K.</Author>
-<Author>Toki, S.</Author>
-<Author>Nakanishi, S.</Author>
-<Author>Ochiai, K.</Author>
-<Author>Ando, K.</Author>
-<Author>Yoshida, M.</Author>
-<Author>Matsuda, Y.</Author>
-<Author>Yamasaki, M.</Author>
-</Authors>
-<Citation>Bioorg. Med. Chem. 4, 115-120, 1996</Citation>
-<Title>MS-271, a novel inhibitor of calmodulin-activated myosin light chain kinase from Streptomyces sp.--I. Isolation, structural determination and biological properties of MS-271.</Title>
-<Xref>DOI:10.1016/0968-0896(95)00175-1</Xref>
-<Xref>PMID:8689231</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Pallaghy, P.K.</Author>
-<Author>He, W.</Author>
-<Author>Jimenez, E.C.</Author>
-<Author>Olivera, B.M.</Author>
-<Author>Norton, R.S.</Author>
-</Authors>
-<Citation>Biochemistry 39, 12845-12852, 2000</Citation>
-<Title>Structures of the contryphan family of cyclic peptides. Role of electrostatic interactions in cis-trans isomerism.</Title>
-<Xref>DOI:10.1021/bi0010930</Xref>
-<Xref>PMID:11041849</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Pallaghy, P.K.</Author>
-<Author>He, W.</Author>
-<Author>Jimenez, E.C.</Author>
-<Author>Olivera, B.M.</Author>
-<Author>Norton, R.S.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, November 1999</Citation>
-<Description>NMR structure of contryphan-SM cyclic peptide (major form - cis).</Description>
-<Xref>PDB:1DFY</Xref>
-<Note>conformation by (1)H-NMR</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>protein-tryptophan epimerase (EC 5.1.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>W</SequenceSpec>
-<Xref>GO:0019128</Xref>
-<Xref>PSI-MOD:00205</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>D-amino acid</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__d-tryptophan__w">MOD_RES D-tryptophan</Feature>
-</Features>
-<Image src="/images/AA0198.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0198.PDB" />
-</Entry>
-<Entry id="AA0199">
-<Header>
-<Code>AA0199</Code>
-<Dates>
-<CreationDate>31-Dec-2007</CreationDate>
-<StrucRevDate>31-Dec-2007</StrucRevDate>
-<TextChngDate>25-Feb-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>D-threonine</Name>
-<SystematicName>(2R,3R)-2-amino-3-hydroxybutanoic acid</SystematicName>
-<Xref>CAS:632-20-2</Xref>
-<Xref>ChEBI:32826</Xref>
-<Xref>PDBHET:DTH</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 7 N 1 O 2</Formula>
-<Weight type="chemical">101.10</Weight>
-<Weight type="physical">101.047678</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0017">
-<Formula>C 0 H 0 N 0 O 0</Formula>
-<Weight type="chemical">0.00</Weight>
-<Weight type="physical">0.000000</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Faulstich, H.</Author>
-<Author>Buku, A.</Author>
-<Author>Bodenmüller, H.</Author>
-<Author>Wieland, T.</Author>
-</Authors>
-<Citation>Biochemistry 19, 3334-3343, 1980</Citation>
-<Title>Virotoxins: actin-binding cyclic peptides of Amanita virosa mushrooms.</Title>
-<Xref>DOI:10.1021/bi00555a036</Xref>
-<Xref>PMID:6893271</Xref>
-<Note>it is not clear from the report whether D-threonine or D-allo-threonine was found; D-threonine is shown</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hallen, H.E.</Author>
-<Author>Luo, H.</Author>
-<Author>Scott-Craig, J.S.</Author>
-<Author>Walton, J.D.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 104, 19097-19101, 2007</Citation>
-<Title>Gene family encoding the major toxins of lethal Amanita mushrooms.</Title>
-<Xref>DOI:10.1073/pnas.0707340104</Xref>
-<Xref>PMID:18025465</Xref>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>protein-threonine 2-epimerase (EC 5.1.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>T</SequenceSpec>
-<Xref>PSI-MOD:00863</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>D-amino acid</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__d-threonine__t">MOD_RES D-threonine</Feature>
-</Features>
-<Image src="/images/AA0199.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0199.PDB" />
-</Entry>
-<Entry id="AA0200">
-<Header>
-<Code>AA0200</Code>
-<Dates>
-<CreationDate>28-Oct-2005</CreationDate>
-<StrucRevDate>28-Oct-2005</StrucRevDate>
-<TextChngDate>25-Feb-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>D-valine</Name>
-<AlternateName>alpha-amino-beta-methylbutyric acid</AlternateName>
-<AlternateName>alpha-aminoisovaleric acid</AlternateName>
-<SystematicName>(R)-2-amino-3-methylbutanoic acid</SystematicName>
-<Xref>CAS:640-68-6</Xref>
-<Xref>ChEBI:30016</Xref>
-<Xref>PDBHET:DVA</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 9 N 1 O 1</Formula>
-<Weight type="chemical">99.13</Weight>
-<Weight type="physical">99.068414</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0020">
-<Formula>C 0 H 0 N 0 O 0</Formula>
-<Weight type="chemical">0.00</Weight>
-<Weight type="physical">0.000000</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Pisarewicz, K.</Author>
-<Author>Mora, D.</Author>
-<Author>Pflueger, F.C.</Author>
-<Author>Fields, G.B.</Author>
-<Author>Mari, F.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 127, 6207-6215, 2005</Citation>
-<Title>Polypeptide chains containing D-gamma-hydroxyvaline.</Title>
-<Xref>DOI:10.1021/ja050088m</Xref>
-<Xref>PMID:15853325</Xref>
-<Note>mass spectrographic, and 1D- and 2D-TOCSY NMR analysis</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>protein-valine epimerase (EC 5.1.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>V</SequenceSpec>
-<Xref>PSI-MOD:00705</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>D-amino acid</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__d-valine__v">MOD_RES D-valine</Feature>
-</Features>
-<Image src="/images/AA0200.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0200.PDB" />
-</Entry>
-<Entry id="AA0201">
-<Header>
-<Code>AA0201</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>20-Nov-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-isoglutamyl-polyglycine</Name>
-<AlternateName>gamma-glutamylpolyglycine</AlternateName>
-<Xref>ChEBI:21343</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 10 N 2 O 4 +</Formula>
-<Weight type="chemical">186.17 +</Weight>
-<Weight type="physical">186.064057 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0006">
-<Formula>C 2 H 3 N 1 O 1 +</Formula>
-<Weight type="chemical">57.05 +</Weight>
-<Weight type="physical">57.021464 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Redeker, V.</Author>
-<Author>Levilliers, N.</Author>
-<Author>Schmitter, J.M.</Author>
-<Author>Le Caer, J.P.</Author>
-<Author>Rossier, J.</Author>
-<Author>Adoutte, A.</Author>
-<Author>Bre, M.H.</Author>
-</Authors>
-<Citation>Science 266, 1688-1691, 1994</Citation>
-<Title>Polyglycylation of tubulin: a posttranslational modification in axonemal microtubules.</Title>
-<Xref>DOI:10.1126/science.7992051</Xref>
-<Xref>PMID:7992051</Xref>
-<Note>mass spectrometric identification; the polyglycine is composed of 3 to 34 residues</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Vinh, J.</Author>
-<Author>Langridge, J.I.</Author>
-<Author>Bre, M.H.</Author>
-<Author>Levilliers, N.</Author>
-<Author>Redeker, V.</Author>
-<Author>Loyaux, D.</Author>
-<Author>Rossier, J.</Author>
-</Authors>
-<Citation>Biochemistry 38, 3133-3139, 1999</Citation>
-<Title>Structural characterization by tandem mass spectrometry of the posttranslational polyglycylation of tubulin.</Title>
-<Xref>DOI:10.1021/bi982304s</Xref>
-<Xref>PMID:10074368</Xref>
-<Note>mass spectrometric characterization; multiple sites are identified</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lalle, M.</Author>
-<Author>Salzano, A.M.</Author>
-<Author>Crescenzi, M.</Author>
-<Author>Pozio, E.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 281, 5137-5148, 2006</Citation>
-<Title>The Giardia duodenalis 14-3-3 protein is post-translationally modified by phosphorylation and polyglycylation of the C-terminal tail.</Title>
-<Xref>DOI:10.1074/jbc.M509673200</Xref>
-<Xref>PMID:16368691</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Rogowski, K.</Author>
-<Author>Juge, F.</Author>
-<Author>van Dijk, J.</Author>
-<Author>Wloga, D.</Author>
-<Author>Strub, J.M.</Author>
-<Author>Levilliers, N.</Author>
-<Author>Thomas, D.</Author>
-<Author>Bré, M.H.</Author>
-<Author>Van Dorsselaer, A.</Author>
-<Author>Gaertig, J.</Author>
-<Author>Janke, C.</Author>
-</Authors>
-<Citation>Cell 137, 1076-1087, 2009</Citation>
-<Title>Evolutionary divergence of enzymatic mechanisms for posttranslational polyglycylation.</Title>
-<Xref>DOI:10.1016/j.cell.2009.05.020</Xref>
-<Xref>PMID:19524510</Xref>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>glycine:protein-glutamate gamma-ligase (ADP-forming) (EC 6.3.2.-)</EnzymeName>
-<EnzymeName>glycine:protein-glutamyl(gamma-polyglycine) N-ligase (ADP-forming) (EC 6.3.2.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>E</SequenceSpec>
-<Xref>GO:0018094</Xref>
-<Xref>PSI-MOD:00206</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="mod_res__5-glutamyl polyglycine__e">MOD_RES 5-glutamyl polyglycine</Feature>
-</Features>
-<Image src="/images/AA0201.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0201.PDB" />
-</Entry>
-<Entry id="AA0202">
-<Header>
-<Code>AA0202</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>13-Sep-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-isoglutamyl-polyglutamic acid</Name>
-<AlternateName>gamma-glutamylpolyglutamic acid</AlternateName>
-</Names>
-<FormulaBlock>
-<Formula>C 10 H 14 N 2 O 6 +</Formula>
-<Weight type="chemical">258.23 +</Weight>
-<Weight type="physical">258.085186 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0006">
-<Formula>C 5 H 7 N 1 O 3 +</Formula>
-<Weight type="chemical">129.12 +</Weight>
-<Weight type="physical">129.042593 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Edde, B.</Author>
-<Author>Rossier, J.</Author>
-<Author>Le Caer, J.P.</Author>
-<Author>Berwald-Netter, Y.</Author>
-<Author>Koulakoff, A.</Author>
-<Author>Gros, F.</Author>
-<Author>Denoulet, P.</Author>
-</Authors>
-<Citation>J. Cell. Biochem. 46, 134-142, 1991</Citation>
-<Title>A combination of posttranslational modifications is responsible for the production of neuronal alpha-tubulin heterogeneity.</Title>
-<Xref>DOI:10.1002/jcb.240460207</Xref>
-<Xref>PMID:1680872</Xref>
-<Note>the polyglutamate is composed of 3 to 6 residues</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Regnard, C.</Author>
-<Author>Desbruyeres, E.</Author>
-<Author>Huet, J.C.</Author>
-<Author>Beauvallet, C.</Author>
-<Author>Pernollet, J.C.</Author>
-<Author>Edde, B.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 275, 15969-15976, 2000</Citation>
-<Title>Polyglutamylation of nucleosome assembly proteins.</Title>
-<Xref>DOI:10.1074/jbc.M000045200</Xref>
-<Xref>PMID:10747868</Xref>
-<Note>monoclonal antibody detection of modification in proteins other than tubulin</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Xiao, H.</Author>
-<Author>El Bissati, K.</Author>
-<Author>Verdier-Pinard, P.</Author>
-<Author>Burd, B.</Author>
-<Author>Zhang, H.</Author>
-<Author>Kim, K.</Author>
-<Author>Fiser, A.</Author>
-<Author>Angeletti, R.H.</Author>
-<Author>Weiss, L.M.</Author>
-</Authors>
-<Citation>J. Proteome Res. 9, 359-372, 2010</Citation>
-<Title>Post-translational modifications to Toxoplasma gondii α- and β-tubulins include novel C-terminal methylation.</Title>
-<Xref>DOI:10.1021/pr900699a</Xref>
-<Xref>PMID:19886702</Xref>
-<Note>detection of multiple glutamylations by mass-spectrometry in reflector mode</Note>
-</ReferenceBlock>
-<Comment>This entry is for L-isoglutamyl-polyglutamic acid where there are 2 to 6 alpha-peptide linked glutamic acid residues attached to a peptide glutamyl residue by an isopeptide bond. For a single glutamic acid attached to a peptide glutamyl residue by an isopeptide bond, see 5-glutamyl glutamic acid, RESID:AA0612.</Comment>
-<SequenceCode>
-<SequenceSpec>E</SequenceSpec>
-<Xref>GO:0018095</Xref>
-<Xref>PSI-MOD:00207</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0202.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0202.PDB" />
-</Entry>
-<Entry id="AA0203">
-<Header>
-<Code>AA0203</Code>
-<Dates>
-<CreationDate>31-Mar-1995</CreationDate>
-<StrucRevDate>31-Mar-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O4'-(phospho-5'-adenosine)-L-tyrosine</Name>
-<AlternateName>5'-adenylic-O-tyrosine</AlternateName>
-<AlternateName>hydrogen 5'-adenylate tyrosine ester</AlternateName>
-<AlternateName>O-adenyl-L-tyrosine</AlternateName>
-<AlternateName>O4'-L-tyrosine 5'-adenosine phosphodiester</AlternateName>
-<SystematicName>(2S)-2-amino-3-[4-(5'-adenosine phosphonoxy)phenyl]propanoic acid</SystematicName>
-<Xref>CAS:93957-03-0</Xref>
-<Xref>ChEBI:83625</Xref>
-<Xref>PDBHET:AMP</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 19 H 21 N 6 O 8 P 1</Formula>
-<Weight type="chemical">492.38</Weight>
-<Weight type="physical">492.115848</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0019">
-<Formula>C 10 H 12 N 5 O 6 P 1</Formula>
-<Weight type="chemical">329.21</Weight>
-<Weight type="physical">329.052520</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Heinrikson, R.L.</Author>
-<Author>Kingdon, H.S.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 246, 1099-1106, 1971</Citation>
-<Title>Primary structure of Escherichia coli glutamine synthetase. II. The complete amino acid sequence of a tryptic heneicosapeptide containing covalently bound adenylic acid.</Title>
-<Xref>PMID:5543675</Xref>
-<Note>chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Müller, M.P.</Author>
-<Author>Peters, H.</Author>
-<Author>Blümer, J.</Author>
-<Author>Blankenfeldt, W.</Author>
-<Author>Goody, R.S.</Author>
-<Author>Itzen, A.</Author>
-</Authors>
-<Citation>Science 329, 946-949, 2010</Citation>
-<Title>The Legionella effector protein DrrA AMPylates the membrane traffic regulator Rab1b.</Title>
-<Xref>DOI:10.1126/science.1192276</Xref>
-<Xref>PMID:20651120</Xref>
-<Note>X-ray diffraction, 1.70 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Muller, M.P.</Author>
-<Author>Peters, H.</Author>
-<Author>Blumer, J.</Author>
-<Author>Blankenfeldt, W.</Author>
-<Author>Goody, R.S.</Author>
-<Author>Itzen, A.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, June 2010</Citation>
-<Description>Crystal structure of RAB1B covalently modified with AMP at Y77.</Description>
-<Xref>PDB:3NKV</Xref>
-<Note>X-ray diffraction, 1.70 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Li, Y.</Author>
-<Author>Al-Eryani, R.</Author>
-<Author>Yarbrough, M.L.</Author>
-<Author>Orth, K.</Author>
-<Author>Ball, H.L.</Author>
-</Authors>
-<Citation>J. Am. Soc. Mass Spectrom. 22, 752-761, 2011</Citation>
-<Title>Characterization of AMPylation on Threonine, Serine, and Tyrosine Using Mass Spectrometry.</Title>
-<Xref>DOI:10.1007/s13361-011-0084-1</Xref>
-<Xref>PMID:21472612</Xref>
-<Note>mass spectrometric detection and characterization of tandem-MS fragmentation</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>Y</SequenceSpec>
-<Xref>GO:0018254</Xref>
-<Xref>PSI-MOD:00208</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__o-amp-tyrosine__y">MOD_RES O-AMP-tyrosine</Feature>
-</Features>
-<Image src="/images/AA0203.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0203.PDB" />
-</Entry>
-<Entry id="AA0204">
-<Header>
-<Code>AA0204</Code>
-<Dates>
-<CreationDate>30-Jun-1995</CreationDate>
-<StrucRevDate>30-Jun-1995</StrucRevDate>
-<TextChngDate>20-May-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-(2-aminovinyl)-D-cysteine</Name>
-<AlternateName>(S,Z)-S-(2-aminovinyl)cysteine</AlternateName>
-<SystematicName>(2S)-2-amino-3-([(Z)-2-aminoethenyl]sulfanyl)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 7 N 2 O 1 S 1</Formula>
-<Weight type="chemical">143.18</Weight>
-<Weight type="physical">143.027909</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005" label="CYS2">
-<Formula>C -1 H -4 N 0 O -2 S -1</Formula>
-<Weight type="chemical">-80.10</Weight>
-<Weight type="physical">-79.993200</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0005 AA0016" label="SER">
-<Formula>C -1 H -4 N 0 O -3 S 0</Formula>
-<Weight type="chemical">-64.04</Weight>
-<Weight type="physical">-64.016044</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Allgaier, H.</Author>
-<Author>Jung, G.</Author>
-<Author>Werner, R.G.</Author>
-<Author>Schneider, U.</Author>
-<Author>Zaehner, H.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 160, 9-22, 1986</Citation>
-<Title>Epidermin: sequencing of a heterodet tetracyclic 21-peptide amide antibiotic.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1986.tb09933.x</Xref>
-<Xref>PMID:3769923</Xref>
-<Note>mass spectrometric, (1)H-NMR, and (13)C-NMR identification; stereochemical determination</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kellner, R.</Author>
-<Author>Jung, G.</Author>
-<Author>Hoerner, T.</Author>
-<Author>Zaehner, H.</Author>
-<Author>Schnell, N.</Author>
-<Author>Entian, K.D.</Author>
-<Author>Goetz, F.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 177, 53-59, 1988</Citation>
-<Title>Gallidermin: a new lanthionine-containing polypeptide antibiotic.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1988.tb14344.x</Xref>
-<Xref>PMID:3181159</Xref>
-<Note>mass spectrometric identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Minami, Y.</Author>
-<Author>Yoshida, K.</Author>
-<Author>Azuma, R.</Author>
-<Author>Urakawa, A.</Author>
-<Author>Kawauchi, T.</Author>
-<Author>Otani, T.</Author>
-<Author>Komiyama, K.</Author>
-<Author>Omura, S.</Author>
-</Authors>
-<Citation>Tetrahedron Lett. 35, 8001-8004, 1994</Citation>
-<Title>Structure of cypemycin, a new peptide antibiotic.</Title>
-<Xref>DOI:10.1016/0040-4039(94)80033-2</Xref>
-<Note>mass spectrometric, (1)H-NMR, and (13)C-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Li, B.</Author>
-<Author>Sher, D.</Author>
-<Author>Kelly, L.</Author>
-<Author>Shi, Y.</Author>
-<Author>Huang, K.</Author>
-<Author>Knerr, P.J.</Author>
-<Author>Joewono, I.</Author>
-<Author>Rusch, D.</Author>
-<Author>Chisholm, S.W.</Author>
-<Author>van der Donk, W.A.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 107, 10430-10435, 2010</Citation>
-<Title>Catalytic promiscuity in the biosynthesis of cyclic peptide secondary metabolites in planktonic marine cyanobacteria.</Title>
-<Xref>DOI:10.1073/pnas.0913677107</Xref>
-<Xref>PMID:20479271</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Claesen, J.</Author>
-<Author>Bibb, M.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 107, 16297-16302, 2010</Citation>
-<Title>Genome mining and genetic analysis of cypemycin biosynthesis reveal an unusual class of posttranslationally modified peptides.</Title>
-<Xref>DOI:10.1073/pnas.1008608107</Xref>
-<Xref>PMID:20805503</Xref>
-<Note>gene sequence for the encoded peptide, biosynthesis; the authors did not have enough material to determine the stereochemistry and assume that it was the D stereoisomer [private communication]</Note>
-</ReferenceBlock>
-<Comment>This cross-link arises from the decarboxylation of the carboxyl-terminal portion of a lanthionine, either L-lanthionine (see RESID:AA0110) or meso-lanthionine (see RESID:AA0111).</Comment>
-<Comment>This residue is acid labile. It may be identified as (2-aminoethyl)-D-cysteine (D-4-thialysine) after hydrogenation with palladium/charcoal catalyst.</Comment>
-<Comment>For the L stereoisomer, see RESID:AA0548. The stereochemistry of the (2-aminovinyl)-cysteine derived from two L-cysteine residues in cypemycin has not been determined.</Comment>
-<GeneratingEnzyme>
-<EnzymeName link="CYS2">peptidyl-cysteine dethiolase (EC 4.4.1.-)</EnzymeName>
-<EnzymeName link="SER">peptidyl-phosphoserine/phosphothreonine dehydratase (EC 4.2.1.-)</EnzymeName>
-<EnzymeName>peptidyl-cysteine dehydroalanine/dehydrobutyrine ligase (EC 6.2.-.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode link="CYS2">
-<SequenceSpec>C, C</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:01849</Xref>
-</SequenceCode>
-<SequenceCode link="SER">
-<SequenceSpec>C, S</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Condition>cross-link 2</Condition>
-<Xref>GO:0018096</Xref>
-<Xref>PSI-MOD:00209</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>lanthionine</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__s-(2-aminovinyl)-d-cysteine (cys-cys)__c__c" link="CYS2">CROSSLNK S-(2-aminovinyl)-D-cysteine (Cys-Cys)</Feature>
-<Feature type="UniProt" key="crosslnk__s-(2-aminovinyl)-d-cysteine (ser-cys)__s__c" link="SER">CROSSLNK S-(2-aminovinyl)-D-cysteine (Ser-Cys)</Feature>
-</Features>
-<Image src="/images/AA0204.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0204.PDB" />
-</Entry>
-<Entry id="AA0205">
-<Header>
-<Code>AA0205</Code>
-<Dates>
-<CreationDate>30-Jun-1995</CreationDate>
-<StrucRevDate>30-Jun-1995</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-cysteine sulfenic acid</Name>
-<AlternateName>(2R)-2-amino-3-(oxido-lambda(4)-sulfanyl)propanoic acid [tautomer]</AlternateName>
-<AlternateName>2-amino-2-carboxyethanesulfenic acid</AlternateName>
-<AlternateName>2-amino-3-sulfinylpropanoic acid [tautomer]</AlternateName>
-<AlternateName>3-sulfenoalanine</AlternateName>
-<AlternateName>cysteine S-oxide [tautomer]</AlternateName>
-<AlternateName>cysteine sulfoxide [tautomer]</AlternateName>
-<AlternateName>cysteine sulphenic acid</AlternateName>
-<AlternateName>S-hydroxycysteine</AlternateName>
-<AlternateName>S-oxocysteine [tautomer]</AlternateName>
-<AlternateName>S-oxycysteine [tautomer]</AlternateName>
-<SystematicName>(2R)-2-amino-3-(hydroxysulfanyl)propanoic acid</SystematicName>
-<Xref>CAS:5722-80-5</Xref>
-<Xref>CAS:73243-12-6</Xref>
-<Xref>ChEBI:61962</Xref>
-<Xref>ChEBI:61973</Xref>
-<Xref>PDBHET:CSO</Xref>
-<Xref>PDBHET:CSX</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 5 N 1 O 2 S 1</Formula>
-<Weight type="chemical">119.14</Weight>
-<Weight type="physical">119.004099</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 0 H 0 N 0 O 1 S 0</Formula>
-<Weight type="chemical">16.00</Weight>
-<Weight type="physical">15.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Poole, L.B.</Author>
-<Author>Claiborne, A.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 264, 12330-12338, 1989</Citation>
-<Title>The non-flavin redox center of the streptococcal NADH peroxidase. II. Evidence for a stabilized cysteine-sulfenic acid.</Title>
-<Xref>PMID:2501303</Xref>
-<Note>mass spectrometric and chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yeh, J.I.</Author>
-<Author>Claiborne, A.</Author>
-<Author>Hol, W.G.J.</Author>
-</Authors>
-<Citation>Biochemistry 35, 9951-9957, 1996</Citation>
-<Title>Structure of the native cysteine-sulfenic acid redox center of enterococcal NADH peroxidase refined at 2.8 Angstroms resolution.</Title>
-<Xref>DOI:10.1021/bi961037s</Xref>
-<Xref>PMID:8756456</Xref>
-<Note>X-ray diffraction, 2.8 angstroms, active cysteine sulfenic acid form</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Crane 3rd, E.J.</Author>
-<Author>Vervoort, J.</Author>
-<Author>Claiborne, A.</Author>
-</Authors>
-<Citation>Biochemistry 36, 8611-8618, 1997</Citation>
-<Title>13C NMR analysis of the cysteine-sulfenic acid redox center of enterococcal NADH peroxidase.</Title>
-<Xref>DOI:10.1021/bi9707990</Xref>
-<Xref>PMID:9214307</Xref>
-<Note>(13)C-NMR characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Choi, H.J.</Author>
-<Author>Kang, S.W.</Author>
-<Author>Yang, C.H.</Author>
-<Author>Rhee, S.G.</Author>
-<Author>Ryu, S.E.</Author>
-</Authors>
-<Citation>Nature Struct. Biol. 5, 400-406, 1998</Citation>
-<Title>Crystal structure of a novel human peroxidase enzyme at 2.0 angstroms resolution.</Title>
-<Xref>DOI:10.1038/nsb0598-400</Xref>
-<Xref>PMID:9587003</Xref>
-<Note>X-ray diffraction, 2.0 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Nagashima, S.</Author>
-<Author>Nakasako, M.</Author>
-<Author>Dohmae, N.</Author>
-<Author>Tsujimura, M.</Author>
-<Author>Takio, K.</Author>
-<Author>Odaka, M.</Author>
-<Author>Yohda, M.</Author>
-<Author>Kamiya, N.</Author>
-<Author>Endo, I.</Author>
-</Authors>
-<Citation>Nature Struct. Biol. 5, 347-351, 1998</Citation>
-<Title>Novel non-heme iron center of nitrile hydratase with a claw setting of oxygen atoms.</Title>
-<Xref>DOI:10.1038/nsb0598-347</Xref>
-<Xref>PMID:9586994</Xref>
-<Note>X-ray diffraction, 1.7 angstroms; mass spectroscopic identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Boschi-Muller, S.</Author>
-<Author>Azza, S.</Author>
-<Author>Sanglier-Cianferani, S.</Author>
-<Author>Talfournier, F.</Author>
-<Author>Van Dorsselaer, A.</Author>
-<Author>Branlant, G.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 275, 35908-35913, 2000</Citation>
-<Title>A sulfenic acid enzyme intermediate is involved in the catalytic mechanism of peptide methionine sulfoxide reductase from Escherichia coli.</Title>
-<Xref>DOI:10.1074/jbc.M006137200</Xref>
-<Xref>PMID:10964927</Xref>
-<Note>sulfenic acid intermediate; the spelling of "Van Dorsselear" in the journal and in the PubMed citation is corrected</Note>
-</ReferenceBlock>
-<Comment>This reactive residue must be stabilized by the protein structure. As a active site it may be reduced to cysteine or cysteine anion and reoxidized during the reaction cycle.</Comment>
-<Comment>The "active site" feature is used if the stable form is the reduced cysteine; the "modified site" feature is used if the stable form is the oxidized cysteine sulfenic acid.</Comment>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>GO:0018171</Xref>
-<Xref>GO:0018324</Xref>
-<Xref>PSI-MOD:00210</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="act_site__cysteine sulfenic acid (-soh) intermediate__c">ACT_SITE Cysteine sulfenic acid (-SOH) intermediate</Feature>
-<Feature type="UniProt" key="act_site__redox-active__c">ACT_SITE Redox-active</Feature>
-<Feature type="UniProt" key="mod_res__cysteine sulfenic acid (-soh)__c">MOD_RES Cysteine sulfenic acid (-SOH)</Feature>
-</Features>
-<Image src="/images/AA0205.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0205.PDB" />
-</Entry>
-<Entry id="AA0206">
-<Header>
-<Code>AA0206</Code>
-<Dates>
-<CreationDate>30-Jun-1995</CreationDate>
-<StrucRevDate>30-Jun-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-(glycyl)-L-cysteine</Name>
-<AlternateName>1-(cystein-S-yl)-glycinate</AlternateName>
-<AlternateName>glycine cysteine thioester</AlternateName>
-<AlternateName>S-(2-amino-1-oxoethyl)cysteine</AlternateName>
-<SystematicName>(2R)-2-amino-3-[(aminoacetyl)sulfanyl]propanoic acid</SystematicName>
-<Xref>ChEBI:22050</Xref>
-</Names>
-<FormulaBlock label="GCX">
-<Formula>C 5 H 7 N 2 O 2 S 1</Formula>
-<Weight type="chemical">159.18</Weight>
-<Weight type="physical">159.022823</Weight>
-</FormulaBlock>
-<FormulaBlock label="GLY">
-<Formula>C 5 H 9 N 2 O 3 S 1</Formula>
-<Weight type="chemical">177.20</Weight>
-<Weight type="physical">177.033388</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0008" link="GCX">
-<Formula>C 0 H -2 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0008" link="GLY">
-<Formula>C 3 H 5 N 1 O 1 S 1</Formula>
-<Weight type="chemical">103.14</Weight>
-<Weight type="physical">103.009185</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Jentsch, S.</Author>
-<Author>McGrath, J.P.</Author>
-<Author>Varshavsky, A.</Author>
-</Authors>
-<Citation>Nature 329, 131-134, 1987</Citation>
-<Title>The yeast DNA repair gene RAD6 encodes a ubiquitin-conjugating enzyme.</Title>
-<Xref>DOI:10.1038/329131a0</Xref>
-<Xref>PMID:3306404</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mossessova, E.</Author>
-<Author>Lima, C.D.</Author>
-</Authors>
-<Citation>Mol. Cell 5, 865-876, 2000</Citation>
-<Title>Ulp1-SUMO crystal structure and genetic analysis reveal conserved interactions and a regulatory element essential for cell growth in yeast.</Title>
-<Xref>PMID:10882122</Xref>
-<Note>X-ray diffraction, 1.60 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mossessova, E.</Author>
-<Author>Lima, C.D.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, April 2000</Citation>
-<Description>X-ray structure of the C-terminal Ulp1 protease domain in complex with Smt3, the yeast ortholog of SUMO.</Description>
-<Xref>PDB:1EUV</Xref>
-<Note>X-ray diffraction, 1.60 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Carvalho, A.F.</Author>
-<Author>Pinto, M.P.</Author>
-<Author>Grou, C.P.</Author>
-<Author>Alencastre, I.S.</Author>
-<Author>Fransen, M.</Author>
-<Author>Sá-Miranda, C.</Author>
-<Author>Azevedo, J.E.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 282, 31267-31272, 2007</Citation>
-<Title>Ubiquitination of mammalian Pex5p, the peroxisomal import receptor.</Title>
-<Xref>DOI:10.1074/jbc.M706325200</Xref>
-<Xref>PMID:17726030</Xref>
-<Note>chemical and directed mutation analysis; thioester formed with a target protein, not an intermediate</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Grou, C.P.</Author>
-<Author>Carvalho, A.F.</Author>
-<Author>Pinto, M.P.</Author>
-<Author>Wiese, S.</Author>
-<Author>Piechura, H.</Author>
-<Author>Meyer, H.E.</Author>
-<Author>Warscheid, B.</Author>
-<Author>Sá-Miranda, C.</Author>
-<Author>Azevedo, J.E.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 283, 14190-14197, 2008</Citation>
-<Title>Members of the E2D (UbcH5) family mediate the ubiquitination of the conserved cysteine of Pex5p, the peroxisomal import receptor.</Title>
-<Xref>DOI:10.1074/jbc.M800402200</Xref>
-<Xref>PMID:18359941</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ågren, D.</Author>
-<Author>Schnell, R.</Author>
-<Author>Oehlmann, W.</Author>
-<Author>Singh, M.</Author>
-<Author>Schneider, G.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 283, 31567-31574, 2008</Citation>
-<Title>Cysteine synthase (CysM) of Mycobacterium tuberculosis is an O-phosphoserine sulfhydrylase: evidence for an alternative cysteine biosynthesis pathway in mycobacteria.</Title>
-<Xref>DOI:10.1074/jbc.M804877200</Xref>
-<Xref>PMID:18799456</Xref>
-<Note>the encoding of an author's name in the PubMed citation is corrected to UTF8</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Jurgenson, C.T.</Author>
-<Author>Burns, K.E.</Author>
-<Author>Begley, T.P.</Author>
-<Author>Ealick, S.E.</Author>
-</Authors>
-<Citation>Biochemistry 47, 10354-10364, 2008</Citation>
-<Title>Crystal structure of a sulfur carrier protein complex found in the cysteine biosynthetic pathway of Mycobacterium tuberculosis.</Title>
-<Xref>DOI:10.1021/bi800915j</Xref>
-<Xref>PMID:18771296</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>O'Leary, S.E.</Author>
-<Author>Jurgenson, C.T.</Author>
-<Author>Ealick, S.E.</Author>
-<Author>Begley, T.P.</Author>
-</Authors>
-<Citation>Biochemistry 47, 11606-11615, 2008</Citation>
-<Title>O-phospho-L-serine and the thiocarboxylated sulfur carrier protein CysO-COSH are substrates for CysM, a cysteine synthase from Mycobacterium tuberculosis.</Title>
-<Xref>DOI:10.1021/bi8013664</Xref>
-<Xref>PMID:18842002</Xref>
-<Note>cysteine thioester linked to a carboxyl terminal glycine is formed by condensation of a carboxyl terminal thioglycine with free phosphoserine</Note>
-</ReferenceBlock>
-<Comment>The formula and records labeled "GCX" refers to a carboxyl end glycine residue thioester cross-linked to a peptidyl cysteine residue.</Comment>
-<Comment>The formula and records labeled "GLY" refers to a carboxyl end glycine residue thioester bonded to a free cysteine. A carboxyl end thioglycine residue (see RESID:AA0265) is converted to this S-(glycyl)-L-cysteine. It then transamidates, transiently forming a peptide bond to a free cysteine (see RESID:AA0529) before the cysteine is released by a peptidase activity.</Comment>
-<SequenceCode link="GCX">
-<SequenceSpec>C, G</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Condition>cross-link 2</Condition>
-<Xref>GO:0018255</Xref>
-<Xref>PSI-MOD:00211</Xref>
-</SequenceCode>
-<SequenceCode link="GLY">
-<SequenceSpec>G</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>PSI-MOD:01777</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>thioester bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="act_site__glycyl thioester intermediate__c" link="GCX">ACT_SITE Glycyl thioester intermediate</Feature>
-<Feature type="UniProt" key="crosslnk__glycyl cysteine thioester (cys-gly) (interchain with g-cter__c" link="GCX">CROSSLNK Glycyl cysteine thioester (Cys-Gly) (interchain with G-Cter ...)</Feature>
-<Feature type="UniProt" key="mod_res__cyso-cysteine adduct__g" link="GLY">MOD_RES CysO-cysteine adduct</Feature>
-</Features>
-<Image src="/images/AA0206.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0206.PDB" />
-</Entry>
-<Entry id="AA0207">
-<Header>
-<Code>AA0207</Code>
-<Dates>
-<CreationDate>30-Jun-1995</CreationDate>
-<StrucRevDate>30-Jun-1995</StrucRevDate>
-<TextChngDate>31-Mar-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-4-hydroxycinnamyl-L-cysteine</Name>
-<AlternateName>cinnamate cysteine thioester</AlternateName>
-<AlternateName>S-para-coumaryl-L-cysteine</AlternateName>
-<SystematicName>(2R)-2-amino-3-([(2E)-3-(4-hydroxyphenyl)prop-2-enoyl]sulfanyl)propanoic acid</SystematicName>
-<Xref>COMe:BIM000151</Xref>
-<Xref>PDBHET:HC4</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 12 H 11 N 1 O 3 S 1</Formula>
-<Weight type="chemical">249.28</Weight>
-<Weight type="physical">249.045964</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 9 H 6 N 0 O 2 S 0</Formula>
-<Weight type="chemical">146.14</Weight>
-<Weight type="physical">146.036779</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hoff, W.D.</Author>
-<Author>Duex, P.</Author>
-<Author>Haard, K.</Author>
-<Author>Devreese, B.</Author>
-<Author>Nugteren-Roodzant, I.M.</Author>
-<Author>Crielaard, W.</Author>
-<Author>Boelens, R.</Author>
-<Author>Kaptein, R.</Author>
-<Author>Van Beeumen, J.</Author>
-<Author>Hellingwerf, K.J.</Author>
-</Authors>
-<Citation>Biochemistry 33, 13959-13962, 1994</Citation>
-<Title>Thiol ester-linked p-coumaric acid as a new photoactive prosthetic group in a protein with rhodopsin-like photochemistry.</Title>
-<Xref>DOI:10.1021/bi00251a001</Xref>
-<Xref>PMID:7947803</Xref>
-<Note>spectrographic characterization; (1)H-NMR and (13)C-NMR identification; the capitalization of "van Beeumen" in the PubMed citation is corrected</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Baca, M.</Author>
-<Author>Borgstahl, G.E.O.</Author>
-<Author>Boissinot, M.</Author>
-<Author>Burke, P.M.</Author>
-<Author>Williams, D.R.</Author>
-<Author>Slater, K.A.</Author>
-<Author>Getzoff, E.D.</Author>
-</Authors>
-<Citation>Biochemistry 33, 14369-14377, 1994</Citation>
-<Title>Complete chemical structure of photoactive yellow protein: novel thioester-linked 4-hydroxycinnamyl chromophore and photocycle chemistry.</Title>
-<Xref>DOI:10.1021/bi00252a001</Xref>
-<Xref>PMID:7981196</Xref>
-<Note>mass spectrometric and chemical characterization; X-ray diffraction, 1.4 angstroms</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>GO:0018097</Xref>
-<Xref>PSI-MOD:00212</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chromoprotein</Keyword>
-<Keyword>hydroxylation</Keyword>
-<Keyword>photoreceptor</Keyword>
-<Keyword>thioester bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__s-(4-hydroxycinnamyl)cysteine__c">MOD_RES S-(4-hydroxycinnamyl)cysteine</Feature>
-</Features>
-<Image src="/images/AA0207.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0207.PDB" />
-</Entry>
-<Entry id="AA0208">
-<Header>
-<Code>AA0208</Code>
-<Dates>
-<CreationDate>30-Jun-1995</CreationDate>
-<StrucRevDate>30-Jun-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>chondroitin sulfate D-glucuronosyl-D-galactosyl-D-galactosyl-D-xylosyl-L-serine</Name>
-<AlternateName>chondroitin 4-sulfate (chondroitin sulfate A)</AlternateName>
-<AlternateName>chondroitin 6-sulfate (chondroitin sulfate C)</AlternateName>
-<SystematicName>poly[beta-1,4-D-glucopyranuronosyl-beta-1,3-(2-acetamido-2-deoxy-4-sulfate-D-galactosyl)]-beta-1,4-D-glucopyranuronosyl-beta-1,3-D-galactosyl-beta-1,3-D-galactosyl-beta-1,4-D-xylosyl-beta-1,3-L-serine; poly[beta-1,4-D-glucopyranuronosyl-beta-1,3-(2-acetamido-2-deoxy-6-sulfate D-galactosyl)]-beta-1,4-D-glucopyranuronosyl-beta-1,3-D-galactosyl-beta-1,3-D-galactosyl-beta-1,4-D-xylosyl-beta-1,3-L-serine</SystematicName>
-<Xref>CAS:24967-93-9</Xref>
-<Xref>CAS:25322-46-7</Xref>
-<Xref>CAS:9007-28-7</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 4 N 1 O 2 +</Formula>
-<Weight type="chemical">86.07 +</Weight>
-<Weight type="physical">86.024203 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 0 H -1 N 0 O 0 +</Formula>
-<Weight type="chemical">-1.01 +</Weight>
-<Weight type="physical">-1.007825 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bourdon, M.A.</Author>
-<Author>Krusius, T.</Author>
-<Author>Campbell, S.</Author>
-<Author>Schwartz, N.B.</Author>
-<Author>Ruoslahti, E.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 84, 3194-3198, 1987</Citation>
-<Title>Identification and synthesis of a recognition signal for the attachment of glycosaminoglycans to proteins.</Title>
-<Xref>DOI:10.1073/pnas.84.10.3194</Xref>
-<Xref>PMID:3472204</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Enghild, J.J.</Author>
-<Author>Salvesen, G.</Author>
-<Author>Hefta, S.A.</Author>
-<Author>Thogersen, I.B.</Author>
-<Author>Rutherfurd, S.</Author>
-<Author>Pizzo, S.V.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 266, 747-751, 1991</Citation>
-<Title>Chondroitin 4-sulfate covalently cross-links the chains of the human blood protein pre-alpha-inhibitor.</Title>
-<Xref>PMID:1898736</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Chirat, F.</Author>
-<Author>Balduyck, M.</Author>
-<Author>Mizon, C.</Author>
-<Author>Laroui, S.</Author>
-<Author>Sautiere, P.</Author>
-<Author>Mizon, J.</Author>
-</Authors>
-<Citation>Int. J. Biochem. 23, 1201-1203, 1991</Citation>
-<Title>A chondroitin-sulfate chain is located on serine-10 of the urinary trypsin inhibitor.</Title>
-<Xref>DOI:10.1016/0020-711X(91)90216-A</Xref>
-<Xref>PMID:1794445</Xref>
-</ReferenceBlock>
-<Comment>The attachment polysaccharide has not been characterized for all forms of the chondroitin sulfate proteoglycans.</Comment>
-<Comment>Chondroitin 4-sulfate, chondroitin sulfate A, is shown.</Comment>
-<Comment>See also RESID:AA0154, RESID:AA0209, RESID:AA0210, RESID:AA0291, RESID:AA0296, RESID:AA0297, RESID:AA0397, RESID:AA0398, RESID:AA0400, RESID:AA0402, RESID:AA0404, RESID:AA0406, and RESID:AA0422 for other O-glycosylated serines.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>protein xylosyltransferase (EC 2.4.2.26)</EnzymeName>
-<EnzymeName>xylosylprotein 4-beta-galactosyltransferase (EC 2.4.1.133)</EnzymeName>
-<EnzymeName>galactosylxylosylprotein 3-beta-galactosyltransferase (EC 2.4.1.134)</EnzymeName>
-<EnzymeName>galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase (EC 2.4.1.135)</EnzymeName>
-<EnzymeName>glucuronylgalactosylproteoglycan beta-1,4-N-acetylgalactosaminyltransferase (EC 2.4.1.174)</EnzymeName>
-<EnzymeName>chondroitin 4-sulfotransferase (EC 2.8.2.5)</EnzymeName>
-<EnzymeName>chondroitin 6-sulfotransferase (EC 2.8.2.17)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>GO:0018402</Xref>
-<Xref>PSI-MOD:00213</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chondroitin sulfate proteoglycan</Keyword>
-<Keyword>glycoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__o-linked (xyl...) (chondroitin sulfate) serine__s">CARBOHYD O-linked (Xyl...) (chondroitin sulfate) serine</Feature>
-<Feature type="UniProt" key="carbohyd__o-linked (xyl...) (glycosaminoglycan) serine__s">CARBOHYD O-linked (Xyl...) (glycosaminoglycan) serine</Feature>
-</Features>
-<Image src="/images/AA0208.GIF" alt="DUMMY.GIF" />
-</Entry>
-<Entry id="AA0209">
-<Header>
-<Code>AA0209</Code>
-<Dates>
-<CreationDate>30-Jun-1995</CreationDate>
-<StrucRevDate>30-Jun-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>dermatan 4-sulfate D-glucuronosyl-D-galactosyl-D-galactosyl-D-xylosyl-L-serine</Name>
-<AlternateName>beta-heparin</AlternateName>
-<AlternateName>chondroitin sulfate B</AlternateName>
-<SystematicName>poly[beta-1,4-L-idopyranuronosyl-alpha-1,3-(2-acetamido-2-deoxy-4-sulfate D-galactosyl)]-beta-1,4-D-glucopyranuronosyl-beta-1,3-D-galactosyl-beta-1,3-D-galactosyl-beta-1,4-D-xylosyl-beta-1,3-L-serine</SystematicName>
-<Xref>CAS:24967-94-0</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 4 N 1 O 2 +</Formula>
-<Weight type="chemical">86.07 +</Weight>
-<Weight type="physical">86.024203 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 0 H -1 N 0 O 0 +</Formula>
-<Weight type="chemical">-1.01 +</Weight>
-<Weight type="physical">-1.007825 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bourdon, M.A.</Author>
-<Author>Krusius, T.</Author>
-<Author>Campbell, S.</Author>
-<Author>Schwartz, N.B.</Author>
-<Author>Ruoslahti, E.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 84, 3194-3198, 1987</Citation>
-<Title>Identification and synthesis of a recognition signal for the attachment of glycosaminoglycans to proteins.</Title>
-<Xref>DOI:10.1073/pnas.84.10.3194</Xref>
-<Xref>PMID:3472204</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Choi, H.U.</Author>
-<Author>Johnson, T.L.</Author>
-<Author>Pal, S.</Author>
-<Author>Tang, L.H.</Author>
-<Author>Rosenberg, L.</Author>
-<Author>Neame, P.J.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 264, 2876-2884, 1989</Citation>
-<Title>Characterization of the dermatan sulfate proteoglycans, DS-PGI and DS-PGII, from bovine articular cartilage and skin isolated by octyl-sepharose chromatography.</Title>
-<Xref>PMID:2914936</Xref>
-</ReferenceBlock>
-<Comment>The attachment polysaccharide has not been characterized for all forms of the chondroitin sulfate proteoglycans.</Comment>
-<Comment>See also RESID:AA0154, RESID:AA0208, RESID:AA0210, RESID:AA0291, RESID:AA0296, RESID:AA0297, RESID:AA0397, RESID:AA0398, RESID:AA0400, RESID:AA0402, RESID:AA0404, RESID:AA0406, and RESID:AA0422 for other O-glycosylated serines.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>protein xylosyltransferase (EC 2.4.2.26)</EnzymeName>
-<EnzymeName>xylosylprotein 4-beta-galactosyltransferase (EC 2.4.1.133)</EnzymeName>
-<EnzymeName>galactosylxylosylprotein 3-beta-galactosyltransferase (EC 2.4.1.134)</EnzymeName>
-<EnzymeName>galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase (EC 2.4.1.135)</EnzymeName>
-<EnzymeName>glucuronylgalactosylproteoglycan beta-1,4-N-acetylgalactosaminyltransferase (EC 2.4.1.174)</EnzymeName>
-<EnzymeName>chondroitin 4-sulfotransferase (EC 2.8.2.5)</EnzymeName>
-<EnzymeName>chondroitin 6-sulfotransferase (EC 2.8.2.17)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>GO:0018403</Xref>
-<Xref>PSI-MOD:00214</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chondroitin sulfate proteoglycan</Keyword>
-<Keyword>dermatan sulfate</Keyword>
-<Keyword>glycoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__o-linked (xyl...) (dermatan sulfate) serine__s">CARBOHYD O-linked (Xyl...) (dermatan sulfate) serine</Feature>
-<Feature type="UniProt" key="carbohyd__o-linked (xyl...) (glycosaminoglycan) serine__s">CARBOHYD O-linked (Xyl...) (glycosaminoglycan) serine</Feature>
-</Features>
-<Image src="/images/AA0209.GIF" alt="DUMMY.GIF" />
-</Entry>
-<Entry id="AA0210">
-<Header>
-<Code>AA0210</Code>
-<Dates>
-<CreationDate>30-Jun-1995</CreationDate>
-<StrucRevDate>30-Jun-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>heparan sulfate D-glucuronosyl-D-galactosyl-D-galactosyl-D-xylosyl-L-serine</Name>
-<AlternateName>heparin</AlternateName>
-<AlternateName>heparitin sulfate</AlternateName>
-<SystematicName>poly[alpha-1,4-(2-sulfate D-glucopyranuronosyl)-beta-1,4-(2-sulfamino-2-deoxy-6-sulfate D-glucosyl)]-beta-1,4-D-glucopyranuronosyl-beta-1,3-D-galactosyl-beta-1,3-D-galactosyl-beta-1,4-D-xylosyl-beta-1,3-L-serine</SystematicName>
-<Xref>CAS:9005-49-6</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 4 N 1 O 2 +</Formula>
-<Weight type="chemical">86.07 +</Weight>
-<Weight type="physical">86.024203 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 0 H -1 N 0 O 0 +</Formula>
-<Weight type="chemical">-1.01 +</Weight>
-<Weight type="physical">-1.007825 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bourdon, M.A.</Author>
-<Author>Krusius, T.</Author>
-<Author>Campbell, S.</Author>
-<Author>Schwartz, N.B.</Author>
-<Author>Ruoslahti, E.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 84, 3194-3198, 1987</Citation>
-<Title>Identification and synthesis of a recognition signal for the attachment of glycosaminoglycans to proteins.</Title>
-<Xref>DOI:10.1073/pnas.84.10.3194</Xref>
-<Xref>PMID:3472204</Xref>
-</ReferenceBlock>
-<Comment>The attachment polysaccharide has not been characterized for all forms of the chondroitin sulfate proteoglycans.</Comment>
-<Comment>The glucosamine 2-amino groups are to some extent acetylated rather than sulfated.</Comment>
-<Comment>See also RESID:AA0154, RESID:AA0208, RESID:AA0209, RESID:AA0291, RESID:AA0296, RESID:AA0297, RESID:AA0397, RESID:AA0398, RESID:AA0400, RESID:AA0402, RESID:AA0404, RESID:AA0406, and RESID:AA0422 for other O-glycosylated serines.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>protein xylosyltransferase (EC 2.4.2.26)</EnzymeName>
-<EnzymeName>xylosylprotein 4-beta-galactosyltransferase (EC 2.4.1.133)</EnzymeName>
-<EnzymeName>galactosylxylosylprotein 3-beta-galactosyltransferase (EC 2.4.1.134)</EnzymeName>
-<EnzymeName>galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase (EC 2.4.1.135)</EnzymeName>
-<EnzymeName>glucuronylgalactosylproteoglycan beta-1,4-N-acetylgalactosaminyltransferase (EC 2.4.1.174)</EnzymeName>
-<EnzymeName>chondroitin 4-sulfotransferase (EC 2.8.2.5)</EnzymeName>
-<EnzymeName>chondroitin 6-sulfotransferase (EC 2.8.2.17)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>GO:0015012</Xref>
-<Xref>GO:0018404</Xref>
-<Xref>PSI-MOD:00215</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chondroitin sulfate proteoglycan</Keyword>
-<Keyword>glycoprotein</Keyword>
-<Keyword>heparan sulfate</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__o-linked (xyl...) (heparan sulfate) serine__s">CARBOHYD O-linked (Xyl...) (heparan sulfate) serine</Feature>
-<Feature type="UniProt" key="carbohyd__o-linked (xyl...) (glycosaminoglycan) serine__s">CARBOHYD O-linked (Xyl...) (glycosaminoglycan) serine</Feature>
-</Features>
-<Image src="/images/AA0210.GIF" alt="DUMMY.GIF" />
-</Entry>
-<Entry id="AA0211">
-<Header>
-<Code>AA0211</Code>
-<Dates>
-<CreationDate>09-Aug-1995</CreationDate>
-<StrucRevDate>09-Aug-1995</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6-formyl-L-lysine</Name>
-<AlternateName>epsilon-formyllysine</AlternateName>
-<AlternateName>N(zeta)-formyllysine</AlternateName>
-<SystematicName>(2S)-2-amino-6-(formylamino)hexanoic acid</SystematicName>
-<Xref>CAS:1190-48-3</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 12 N 2 O 2</Formula>
-<Weight type="chemical">156.19</Weight>
-<Weight type="physical">156.089878</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 1 H 0 N 0 O 1</Formula>
-<Weight type="chemical">28.01</Weight>
-<Weight type="physical">27.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Doonan, S.</Author>
-<Author>Garman, A.J.</Author>
-<Author>Hanson, J.M.</Author>
-<Author>Loudon, A.G.</Author>
-<Author>Vernon, C.A.</Author>
-</Authors>
-<Citation>J. Chem. Soc. Perkin Trans. I 1978, 1157-1160, 1978</Citation>
-<Title>Identification by mass spectrometry of N(epsilon)-formyl-lysine residues in a peptide from bee venom.</Title>
-<Xref>DOI:10.1039/P19780001157</Xref>
-<Note>mass spectrometric identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Jiang, T.</Author>
-<Author>Zhou, X.</Author>
-<Author>Taghizadeh, K.</Author>
-<Author>Dong, M.</Author>
-<Author>Dedon, P.C.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 104, 60-65, 2007</Citation>
-<Title>N-formylation of lysine in histone proteins as a secondary modification arising from oxidative DNA damage.</Title>
-<Xref>DOI:10.1073/pnas.0606775103</Xref>
-<Xref>PMID:17190813</Xref>
-<Note>N6-formyllysine in histone is formed as an artifact of oxidative DNA damage</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wiśniewski, J.R.</Author>
-<Author>Zougman, A.</Author>
-<Author>Mann, M.</Author>
-</Authors>
-<Citation>Nucleic Acids Res. 36, 570-577, 2008</Citation>
-<Title>N(epsilon)-formylation of lysine is a widespread post-translational modification of nuclear proteins occurring at residues involved in regulation of chromatin function.</Title>
-<Xref>DOI:10.1093/nar/gkm1057</Xref>
-<Xref>PMID:18056081</Xref>
-<Note>mass spectrometric identification; distinguishes from nominally isobaric N6,N6-dimethyllysine (see RESID:AA0075); care was taken not to expose the sample to either formic acid or formaldehyde, however oxidation of N6-methyllysine was not precluded; the encoding of an author's name in the PubMed citation is corrected to UTF8</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>GO:0018257</Xref>
-<Xref>PSI-MOD:00216</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>formylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n6-formyllysine__k">MOD_RES N6-formyllysine</Feature>
-</Features>
-<Image src="/images/AA0211.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0211.PDB" />
-</Entry>
-<Entry id="AA0212">
-<Header>
-<Code>AA0212</Code>
-<Dates>
-<CreationDate>18-Aug-1995</CreationDate>
-<StrucRevDate>28-Oct-2005</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O4-arabinosyl-L-hydroxyproline</Name>
-<AlternateName>4-(beta-L-arabinofuranosyloxy)proline</AlternateName>
-<AlternateName>beta-arabinofuranosyl-4-hydroxyproline</AlternateName>
-<AlternateName>O4-glycosyl-hydroxyproline</AlternateName>
-<SystematicName>(2S,4R)-4-(beta-L-arabinofuranosyloxy)pyrrolidine-2-carboxylic acid</SystematicName>
-<Xref>ChEBI:131610</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 10 H 15 N 1 O 6 +</Formula>
-<Weight type="chemical">245.23 +</Weight>
-<Weight type="physical">245.089937 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0015">
-<Formula>C 5 H 8 N 0 O 5 +</Formula>
-<Weight type="chemical">148.11 +</Weight>
-<Weight type="physical">148.037173 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Allen, A.K.</Author>
-<Author>Desai, N.N.</Author>
-<Author>Neuberger, A.</Author>
-<Author>Creeth, J.M.</Author>
-</Authors>
-<Citation>Biochem. J. 171, 665-674, 1978</Citation>
-<Title>Properties of potato lectin and the nature of its glycoprotein linkages.</Title>
-<Xref>PMID:666730</Xref>
-<Note>the modification is identified as beta-L-arabinofuranosyloxy-4-proline</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kieliszewski, M.J.</Author>
-<Author>O'Neill, M.</Author>
-<Author>Leykam, J.</Author>
-<Author>Orlando, R.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 270, 2541-2549, 1995</Citation>
-<Title>Tandem mass spectrometry and structural elucidation of glycopeptides from a hydroxyproline-rich plant cell wall glycoprotein indicate that contiguous hydroxyproline residues are the major sites of hydroxyproline O-arabinosylation.</Title>
-<Xref>DOI:10.1074/jbc.270.6.2541</Xref>
-<Xref>PMID:7852316</Xref>
-<Note>mass spectrometric detection; the glycan in plant hydroxyproline-rich cell wall glycoprotein typically consists of 1 to 5 arabinose units 1-2 alpha-linked</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ogawa-Ohnishi, M.</Author>
-<Author>Matsushita, W.</Author>
-<Author>Matsubayashi, Y.</Author>
-</Authors>
-<Citation>Nature Chem. Biol. 9, 726-730, 2013</Citation>
-<Title>Identification of three hydroxyproline O-arabinosyltransferases in Arabidopsis thaliana.</Title>
-<Xref>DOI:10.1038/nchembio.1351</Xref>
-<Xref>PMID:24036508</Xref>
-<Note>biosynthesis</Note>
-</ReferenceBlock>
-<Comment>See also RESID:AA0389 and RESID:AA0390 for other O4-glycosylated 4-hydroxyprolines.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>hydroxyproline O-arabinosyltransferase</EnzymeName>
-<EnzymeName>UDP-β-L-arabinofuranose:[protein]-trans-4-hydroxy-L-proline L-arabinofuranosyl transferase (configuration-retaining) (EC 2.4.2.58)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>P</SequenceSpec>
-<Condition>secondary to RESID:AA0030</Condition>
-<Xref>GO:0006493</Xref>
-<Xref>GO:0018258</Xref>
-<Xref>PSI-MOD:00217</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__o-linked (ara...) hydroxyproline__p">CARBOHYD O-linked (Ara...) hydroxyproline</Feature>
-</Features>
-<Image src="/images/AA0212.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0212.PDB" />
-</Entry>
-<Entry id="AA0213">
-<Header>
-<Code>AA0213</Code>
-<Dates>
-<CreationDate>18-Aug-1995</CreationDate>
-<StrucRevDate>28-Feb-1997</StrucRevDate>
-<TextChngDate>20-May-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-(phospho-5'-RNA)-L-serine</Name>
-<AlternateName>O3-(phospho-5'-RNA)-L-serine</AlternateName>
-<AlternateName>O3-L-serine 5'-RNA phosphodiester</AlternateName>
-<SystematicName>(S)-2-amino-3-(5'-ribonucleic acid phosphonoxy)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 5 N 1 O 5 P 1 +</Formula>
-<Weight type="chemical">166.05 +</Weight>
-<Weight type="physical">165.990534 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 0 H 0 N 0 O 3 P 1 +</Formula>
-<Weight type="chemical">78.97 +</Weight>
-<Weight type="physical">78.958505 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Samad, A.</Author>
-<Author>Carroll, R.B.</Author>
-</Authors>
-<Citation>Mol. Cell. Biol. 11, 1598-1606, 1991</Citation>
-<Title>The tumor suppressor p53 is bound to RNA by a stable covalent linkage.</Title>
-<Xref>DOI:10.1128/MCB.11.3.1598</Xref>
-<Xref>PMID:1705009</Xref>
-<Note>chromatographic detection; chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Olspert, A.</Author>
-<Author>Peil, L.</Author>
-<Author>Hébrard, E.</Author>
-<Author>Fargette, D.</Author>
-<Author>Truve, E.</Author>
-</Authors>
-<Citation>J. Gen. Virol. 92, 445-452, 2011</Citation>
-<Title>Protein-RNA linkage and post-translational modifications of two sobemovirus VPgs.</Title>
-<Xref>DOI:10.1099/vir.0.026476-0</Xref>
-<Xref>PMID:21068217</Xref>
-<Note>mass spectrometric identification; for the genome-linked protein (VPg) of rice yellow mottle virus, the 5'-end is adenosine and pAp was identified attached to Ser-1</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>GO:0018259</Xref>
-<Xref>PSI-MOD:00218</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>genome-linked protein</Keyword>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__o-(5&apos;-phospho-rna)-serine__s">MOD_RES O-(5'-phospho-RNA)-serine</Feature>
-</Features>
-<Image src="/images/AA0213.GIF" alt="DUMMY.GIF" />
-</Entry>
-<Entry id="AA0214">
-<Header>
-<Code>AA0214</Code>
-<Dates>
-<CreationDate>25-Aug-1995</CreationDate>
-<StrucRevDate>25-Aug-1995</StrucRevDate>
-<TextChngDate>31-Dec-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-citrulline</Name>
-<AlternateName>2-amino-5-(aminocarbonyl)aminopentanoic acid</AlternateName>
-<AlternateName>alpha-amino-delta-ureidovaleric acid</AlternateName>
-<AlternateName>delta-ureidonorvaline</AlternateName>
-<AlternateName>N5-(aminocarbonyl)ornithine</AlternateName>
-<AlternateName>N5-carbamoylornithine</AlternateName>
-<AlternateName>N5-carbamylornithine</AlternateName>
-<SystematicName>(S)-2-amino-5-(carbamoylamino)pentanoic acid</SystematicName>
-<Xref>CAS:372-75-8</Xref>
-<Xref>PDBHET:CIR</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 11 N 3 O 2</Formula>
-<Weight type="chemical">157.17</Weight>
-<Weight type="physical">157.085127</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0002">
-<Formula>C 0 H -1 N -1 O 1</Formula>
-<Weight type="chemical">0.98</Weight>
-<Weight type="physical">0.984016</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wood, D.D.</Author>
-<Author>Moscarello, M.A.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 264, 5121-5127, 1989</Citation>
-<Title>The isolation, characterization, and lipid-aggregating properties of a citrulline containing myelin basic protein.</Title>
-<Xref>PMID:2466844</Xref>
-<Note>chromatographic identification; the mechanism for non-specific formation of citrulline from arginine in myelin is not known, but is probably artifactual</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Loos, T.</Author>
-<Author>Mortier, A.</Author>
-<Author>Gouwy, M.</Author>
-<Author>Ronsse, I.</Author>
-<Author>Put, W.</Author>
-<Author>Lenaerts, J.P.</Author>
-<Author>Van Damme, J.</Author>
-<Author>Proost, P.</Author>
-</Authors>
-<Citation>Blood 112, 2648-2656, 2008</Citation>
-<Title>Citrullination of CXCL10 and CXCL11 by peptidylarginine deiminase: a naturally occurring posttranslational modification of chemokines and new dimension of immunoregulation.</Title>
-<Xref>DOI:10.1182/blood-2008-04-149039</Xref>
-<Xref>PMID:18645041</Xref>
-<Note>the deimination of a specific arginine in a protein by peptidylarginine deiminase is established</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>protein-arginine deiminase (EC 3.5.3.15)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>R</SequenceSpec>
-<Xref>GO:0018101</Xref>
-<Xref>PSI-MOD:00219</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>citrulline</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__citrulline__r">MOD_RES Citrulline</Feature>
-</Features>
-<Image src="/images/AA0214.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0214.PDB" />
-</Entry>
-<Entry id="AA0215">
-<Header>
-<Code>AA0215</Code>
-<Dates>
-<CreationDate>03-Nov-1995</CreationDate>
-<StrucRevDate>03-Nov-1995</StrucRevDate>
-<TextChngDate>31-Jul-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>4-hydroxy-L-arginine</Name>
-<AlternateName>2-amino-5-(carbamimidamido)-4-hydroxypentanoic acid [tautomer]</AlternateName>
-<AlternateName>2-amino-5-guanidino-4-hydroxypentanoic acid</AlternateName>
-<AlternateName>2-amino-5-[(aminoiminomethyl)amino]-4-hydroxypentanoic acid [tautomer]</AlternateName>
-<AlternateName>C(gamma)-hydroxyarginine</AlternateName>
-<AlternateName>gamma-hydroxyarginine</AlternateName>
-<SystematicName>(2S,4Xi)-2-amino-5-[(diaminomethylidene)amino]-4-hydroxypentanoic acid</SystematicName>
-<Xref>CAS:2524-31-4</Xref>
-<Xref>CAS:61370-10-3</Xref>
-<Xref>PDBHET:ARO</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 12 N 4 O 2</Formula>
-<Weight type="chemical">172.19</Weight>
-<Weight type="physical">172.096026</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0002">
-<Formula>C 0 H 0 N 0 O 1</Formula>
-<Weight type="chemical">16.00</Weight>
-<Weight type="physical">15.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Papov, V.V.</Author>
-<Author>Diamond, T.V.</Author>
-<Author>Biemann, K.</Author>
-<Author>Waite, J.H.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 270, 20183-20192, 1995</Citation>
-<Title>Hydroxyarginine-containing polyphenolic proteins in the adhesive plaques of the marine mussel Mytilus edulis.</Title>
-<Xref>DOI:10.1074/jbc.270.34.20183</Xref>
-<Xref>PMID:7650037</Xref>
-<Note>chromatographic detection; mass spectrometric and chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Haenzelmann, P.</Author>
-<Author>Dobbek, H.</Author>
-<Author>Gremer, L.</Author>
-<Author>Huber, R.</Author>
-<Author>Meyer, O.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 301, 1221-1235, 2000</Citation>
-<Title>The effect of intracellular molybdenum in Hydrogenophaga pseudoflava on the crystallographic structure of the seleno-molybdo-iron-sulfur flavoenzyme carbon monoxide dehydrogenase.</Title>
-<Xref>DOI:10.1006/jmbi.2000.4023</Xref>
-<Xref>PMID:10966817</Xref>
-<Note>X-ray diffraction, 2.25 angstroms; an arginine residue involved in binding molybdopterin appears to be modified to (2S,4R)-4-hydroxyarginine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Haenzelmann, P.</Author>
-<Author>Dobbek, H.</Author>
-<Author>Gremer, L.</Author>
-<Author>Huber, R.</Author>
-<Author>Meyer, O.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, September 2000</Citation>
-<Description>Carbon monoxide dehydrogenase from Hydrogenophaga pseudoflava.</Description>
-<Xref>PDB:1FFV</Xref>
-<Note>X-ray diffraction, 2.25 angstroms</Note>
-</ReferenceBlock>
-<Comment>The stereochemistry for the second chiral center has not been resolved. The (2S,4R) diastereomer is shown.</Comment>
-<SequenceCode>
-<SequenceSpec>R</SequenceSpec>
-<Xref>GO:0018102</Xref>
-<Xref>PSI-MOD:00220</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__4-hydroxyarginine__r">MOD_RES 4-hydroxyarginine</Feature>
-</Features>
-<Image src="/images/AA0215.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0215.PDB" />
-</Entry>
-<Entry id="AA0216">
-<Header>
-<Code>AA0216</Code>
-<Dates>
-<CreationDate>01-Sep-1995</CreationDate>
-<StrucRevDate>01-Sep-1995</StrucRevDate>
-<TextChngDate>20-Nov-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-(L-isoaspartyl)-L-cysteine</Name>
-<AlternateName>2-(3-amino-3-carboxypropanoyl)amino-3-mercaptopropanoic acid</AlternateName>
-<AlternateName>2-amino-N4-(1-carboxy-2-mercaptoethyl)butanediamic acid</AlternateName>
-<AlternateName>N-beta-aspartylcysteine</AlternateName>
-<AlternateName>N-isoaspartyl cysteine</AlternateName>
-<SystematicName>(S)-2-amino-4-((R)-1-carboxy-2-sulfanylethyl)amino-4-oxobutanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 9 N 2 O 3 S 1</Formula>
-<Weight type="chemical">201.22</Weight>
-<Weight type="physical">201.033388</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0003">
-<Formula>C 0 H -3 N -1 O 0 S 0</Formula>
-<Weight type="chemical">-17.03</Weight>
-<Weight type="physical">-17.026549</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Frechet, D.</Author>
-<Author>Guitton, J.D.</Author>
-<Author>Herman, F.</Author>
-<Author>Faucher, D.</Author>
-<Author>Helynck, G.</Author>
-<Author>Monegier du Sorbier, B.</Author>
-<Author>Ridoux, J.P.</Author>
-<Author>James-Surcouf, E.</Author>
-<Author>Vuilhorgne, M.</Author>
-</Authors>
-<Citation>Biochemistry 33, 42-50, 1994</Citation>
-<Title>Solution structure of RP 71955, a new 21 amino acid tricyclic peptide active against HIV-1 virus.</Title>
-<Xref>DOI:10.1021/bi00167a006</Xref>
-<Xref>PMID:8286361</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Frechet, D.</Author>
-<Author>Guitton, J.D.</Author>
-<Author>Herman, F.</Author>
-<Author>Faucher, D.</Author>
-<Author>Helynck, G.</Author>
-<Author>Monegier du Sorbier, B.</Author>
-<Author>Ridoux, J.P.</Author>
-<Author>James-Surcouf, E.</Author>
-<Author>Vuilhorgne, M.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, August 1993</Citation>
-<Description>Solution structure of RP 71955, a new 21 amino acid tricyclic peptide active against HIV-1 virus.</Description>
-<Xref>PDB:1RPB</Xref>
-<Note>conformation by (1)H-NMR</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>C, N</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Condition>cross-link 2</Condition>
-<Xref>GO:0018263</Xref>
-<Xref>PSI-MOD:00221</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-<Keyword>isopeptide bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__isoaspartyl cysteine isopeptide (cys-asn)__c__n">CROSSLNK Isoaspartyl cysteine isopeptide (Cys-Asn)</Feature>
-</Features>
-<Image src="/images/AA0216.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0216.PDB" />
-</Entry>
-<Entry id="AA0217">
-<Header>
-<Code>AA0217</Code>
-<Dates>
-<CreationDate>01-Sep-1995</CreationDate>
-<StrucRevDate>24-Jul-1997</StrucRevDate>
-<TextChngDate>20-Apr-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>2'-mannosyl-L-tryptophan</Name>
-<AlternateName>2'-tryptophan C-mannoside</AlternateName>
-<SystematicName>(2S)-2-amino-3-(2-beta-D-mannopyranosyl-1H-indol-3-yl)propanoic acid</SystematicName>
-<Xref>PDBHET:BMA</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 17 H 20 N 2 O 6</Formula>
-<Weight type="chemical">348.36</Weight>
-<Weight type="physical">348.132136</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0018">
-<Formula>C 6 H 10 N 0 O 5</Formula>
-<Weight type="chemical">162.14</Weight>
-<Weight type="physical">162.052823</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hofsteenge, J.</Author>
-<Author>Mueller, D.R.</Author>
-<Author>de Beer, T.</Author>
-<Author>Loeffler, A.</Author>
-<Author>Richter, W.J.</Author>
-<Author>Vliegenthart, J.F.G.</Author>
-</Authors>
-<Citation>Biochemistry 33, 13524-13530, 1994</Citation>
-<Title>New type of linkage between a carbohydrate and a protein: C-glycosylation of a specific tryptophan residue in human RNase U-s.</Title>
-<Xref>DOI:10.1021/bi00250a003</Xref>
-<Xref>PMID:7947762</Xref>
-<Note>mass spectrometric, (1)H-NMR, and (13)C-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>de Beer, T.</Author>
-<Author>Vliegenthart, J.F.</Author>
-<Author>Loffler, A.</Author>
-<Author>Hofsteenge, J.</Author>
-</Authors>
-<Citation>Biochemistry 34, 11785-11789, 1995</Citation>
-<Title>The hexopyranosyl residue that is C-glycosidically linked to the side chain of tryptophan-7 in human RNase Us is alpha-mannopyranose.</Title>
-<Xref>DOI:10.1021/bi00037a016</Xref>
-<Xref>PMID:7547911</Xref>
-<Note>(1)H-NMR and (13)C-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lovelace, L.L.</Author>
-<Author>Cooper, C.L.</Author>
-<Author>Sodetz, J.M.</Author>
-<Author>Lebioda, L.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 286, 17585-17592, 2011</Citation>
-<Title>Structure of human C8 protein provides mechanistic insight into membrane pore formation by complement.</Title>
-<Xref>DOI:10.1074/jbc.M111.219766</Xref>
-<Xref>PMID:21454577</Xref>
-<Note>X-ray diffraction, 2.51 angstroms; the authors note that the multiple sites of mannosylated tryptophan are fit better by the beta anomeric structure</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lovelace, L.L.</Author>
-<Author>Cooper, C.L.</Author>
-<Author>Sodetz, J.M.</Author>
-<Author>Lebioda, L.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, August 2010</Citation>
-<Description>Crystal structure of human complement component C8.</Description>
-<Xref>PDB:3OJY</Xref>
-<Note>X-ray diffraction, 2.51 angstroms</Note>
-</ReferenceBlock>
-<Comment>The carbohydrate, identified as mannose, is linked to tryptophan by an unusual C-glycosidic linkage.</Comment>
-<Comment>The structures determined in NMR and X-ray diffraction studies differ in assigning the glycosylation as being alpha or beta, respectively.  The beta anomeric form is shown.</Comment>
-<SequenceCode>
-<SequenceSpec>W</SequenceSpec>
-<Xref>GO:0018103</Xref>
-<Xref>GO:0018406</Xref>
-<Xref>PSI-MOD:00222</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__c-linked (man)__w">CARBOHYD C-linked (Man)</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="carbohyd__c-linked (hex)__w">CARBOHYD C-linked (Hex)</Feature>
-<Note>this UniProt feature is used when the identity of the sugar has not been determined</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0217.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0217.PDB" />
-</Entry>
-<Entry id="AA0218">
-<Header>
-<Code>AA0218</Code>
-<Dates>
-<CreationDate>01-Sep-1995</CreationDate>
-<StrucRevDate>01-Sep-1995</StrucRevDate>
-<TextChngDate>30-Apr-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6-mureinyl-L-lysine</Name>
-<AlternateName>N6-[(2R,6S)-2-(N-(N-mureinyl-(R)-alanyl)-(S)-glutamyl)amino-6-amino-6-carboxy-1-oxohex-1-yl]lysine</AlternateName>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 11 N 2 O 1 +</Formula>
-<Weight type="chemical">127.17 +</Weight>
-<Weight type="physical">127.087138 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 0 H -1 N 0 O 0 +</Formula>
-<Weight type="chemical">-1.01 +</Weight>
-<Weight type="physical">-1.007825 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Braun, V.</Author>
-<Author>Bosch, V.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 28, 51-69, 1972</Citation>
-<Title>Sequence of the murein-lipoprotein and the attachment site of the lipid.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1972.tb01883.x</Xref>
-<Xref>PMID:4261992</Xref>
-<Note>chemical characterization</Note>
-</ReferenceBlock>
-<Comment>The epsilon-amino group of lysine is covalently linked to bacterial cell wall murein by a peptide-like L-alanyl-D-glutamyl-2,6-diaminopimelic acid linkage.</Comment>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>GO:0019121</Xref>
-<Xref>PSI-MOD:00223</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>peptidoglycan</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n6-murein peptidoglycan lysine__k">MOD_RES N6-murein peptidoglycan lysine</Feature>
-</Features>
-<Image src="/images/AA0218.GIF" alt="DUMMY.GIF" />
-</Entry>
-<Entry id="AA0219">
-<Header>
-<Code>AA0219</Code>
-<Dates>
-<CreationDate>19-May-2000</CreationDate>
-<StrucRevDate>19-May-2000</StrucRevDate>
-<TextChngDate>31-Mar-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>1-chondroitin sulfate-L-aspartic acid ester</Name>
-<AlternateName>1-aspartic acid ester with 6-chondroitin 4-sulfate</AlternateName>
-<AlternateName>poly[beta-1,4-D-glucopyranuronosyl-beta-1,3-(2-acetamido-2-deoxy-4-sulfate D-galactosyl)]beta-1,4-D-glucopyranuronosyl-beta-1,3-(2-acetamido-2-deoxy-4-sulfate-6-(1-L-aspartyl)-D-galactose)</AlternateName>
-<AlternateName>protein-glycosaminoglycan-protein cross-link</AlternateName>
-</Names>
-<FormulaBlock>
-<Formula>C 18 H 25 N 2 O 17 S 1 +</Formula>
-<Weight type="chemical">573.45 +</Weight>
-<Weight type="physical">573.087393 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0004">
-<Formula>C 14 H 19 N 1 O 13 S 1 +</Formula>
-<Weight type="chemical">441.36 +</Weight>
-<Weight type="physical">441.057711 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Enghild, J.J.</Author>
-<Author>Salvesen, G.</Author>
-<Author>Hefta, S.A.</Author>
-<Author>Thogersen, I.B.</Author>
-<Author>Rutherfurd, S.</Author>
-<Author>Pizzo, S.V.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 266, 747-751, 1991</Citation>
-<Title>Chondroitin 4-sulfate covalently cross-links the chains of the human blood protein pre-alpha-inhibitor.</Title>
-<Xref>PMID:1898736</Xref>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>D</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0019800</Xref>
-<Xref>PSI-MOD:00224</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>chondroitin sulfate proteoglycan</Keyword>
-<Keyword>glycoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__aspartate 1-(chondroitin 4-sulfate)-ester__d">MOD_RES Aspartate 1-(chondroitin 4-sulfate)-ester</Feature>
-</Features>
-<Image src="/images/AA0219.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0219.PDB" />
-</Entry>
-<Entry id="AA0220">
-<Header>
-<Code>AA0220</Code>
-<Dates>
-<CreationDate>01-Sep-1995</CreationDate>
-<StrucRevDate>01-Sep-1995</StrucRevDate>
-<TextChngDate>30-Apr-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-(6-FMN)-L-cysteine</Name>
-<AlternateName>6-[S-cysteinyl]flavin mononucleotide</AlternateName>
-<AlternateName>6-[S-cysteinyl]FMN</AlternateName>
-<SystematicName>(R)-2-amino-3-[6-riboflavin 5'-dihydrogen phosphate]sulfanylpropanoic acid</SystematicName>
-<Xref>COMe:BIM000137</Xref>
-<Xref>PDBHET:FMN</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 20 H 24 N 5 O 10 P 1 S 1</Formula>
-<Weight type="chemical">557.47</Weight>
-<Weight type="physical">557.098150</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 17 H 19 N 4 O 9 P 1 S 0</Formula>
-<Weight type="chemical">454.33</Weight>
-<Weight type="physical">454.088965</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kenney, W.C.</Author>
-<Author>McIntire, W.</Author>
-<Author>Steenkamp, D.J.</Author>
-<Author>Benisek, W.F.</Author>
-</Authors>
-<Citation>FEBS Lett. 85, 137-140, 1978</Citation>
-<Title>Amino acid sequence of a cofactor peptide from trimethylamine dehydrogenase.</Title>
-<Xref>DOI:10.1016/0014-5793(78)81265-4</Xref>
-<Xref>PMID:620783</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Barber, M.J.</Author>
-<Author>Neame, P.J.</Author>
-<Author>Lim, L.W.</Author>
-<Author>White, S.</Author>
-<Author>Matthews, F.S.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 267, 6611-6619, 1992</Citation>
-<Title>Correlation of X-ray deduced and experimental amino acid sequences of trimethylamine dehydrogenase.</Title>
-<Xref>PMID:1551870</Xref>
-<Note>X-ray diffraction, 2.4 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mathews, F.S.</Author>
-<Author>Lim, L.W.</Author>
-<Author>White, S.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, October 1993</Citation>
-<Description>Correlation of X-ray deduced and experimental amino acid sequences of trimethylamine dehydrogenase.</Description>
-<Xref>PDB:2TMD</Xref>
-<Note>X-ray diffraction, 2.4 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Trickey, P.</Author>
-<Author>Basran, J.</Author>
-<Author>Lian, L.Y.</Author>
-<Author>Chen, Z.</Author>
-<Author>Barton, J.D.</Author>
-<Author>Sutcliffe, M.J.</Author>
-<Author>Scrutton, N.S.</Author>
-<Author>Mathews, F.S.</Author>
-</Authors>
-<Citation>Biochemistry 39, 7678-7688, 2000</Citation>
-<Title>Structural and biochemical characterization of recombinant wild type and a C30A mutant of trimethylamine dehydrogenase from methylophilus methylotrophus (sp. W(3)A(1)).</Title>
-<Xref>DOI:10.1021/bi9927181</Xref>
-<Xref>PMID:10869173</Xref>
-<Note>X-ray diffraction, 2.2 angstroms</Note>
-</ReferenceBlock>
-<Comment>The keyword "phosphoprotein" is not used with flavin modifications linked through the flavin.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>GO:0018310</Xref>
-<Xref>PSI-MOD:00225</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>*phosphoprotein</Keyword>
-<Keyword>flavoprotein</Keyword>
-<Keyword>FMN</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__s-6-fmn cysteine__c">MOD_RES S-6-FMN cysteine</Feature>
-</Features>
-<Image src="/images/AA0220.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0220.PDB" />
-</Entry>
-<Entry id="AA0221">
-<Header>
-<Code>AA0221</Code>
-<Dates>
-<CreationDate>01-Sep-1995</CreationDate>
-<StrucRevDate>01-Sep-1995</StrucRevDate>
-<TextChngDate>31-Mar-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>1'-(8alpha-FAD)-L-histidine</Name>
-<AlternateName>8alpha-(N(epsilon)-histidyl)FAD</AlternateName>
-<AlternateName>8alpha-(N1'-histidyl)FAD</AlternateName>
-<AlternateName>8alpha-N3-histidyl FAD [misnomer]</AlternateName>
-<AlternateName>N(tau)-(8alpha-FAD)-histidine</AlternateName>
-<AlternateName>tele-(8alpha-FAD)-histidine</AlternateName>
-<SystematicName>(S)-2-amino-3-(1-[8alpha riboflavin 5'-(trihydrogen diphosphate) 5'-&gt;5'-ester with adenosine]imidazol-4-yl)propanoic acid</SystematicName>
-<Xref>COMe:BIM000138</Xref>
-<Xref>PDBHET:FAD</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 33 H 38 N 12 O 16 P 2</Formula>
-<Weight type="chemical">920.68</Weight>
-<Weight type="physical">920.200396</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0009">
-<Formula>C 27 H 31 N 9 O 15 P 2</Formula>
-<Weight type="chemical">783.54</Weight>
-<Weight type="physical">783.141485</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Walker, W.H.</Author>
-<Author>Singer, T.P.</Author>
-<Author>Ghisla, S.</Author>
-<Author>Hemmerich, P.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 26, 279-289, 1972</Citation>
-<Title>Studies on succinate dehydrogenase. 8alpha-Histidyl-FAD as the active center of succinate dehydrogenase.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1972.tb01766.x</Xref>
-<Xref>PMID:4339951</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Pinto, J.T.</Author>
-<Author>Frisell, W.R.</Author>
-</Authors>
-<Citation>Arch. Biochem. Biophys. 169, 483-491, 1975</Citation>
-<Title>Characterization of the peptide-bound flavin of a bacterial sarcosine dehydrogenase.</Title>
-<Xref>DOI:10.1016/0003-9861(75)90191-5</Xref>
-<Xref>PMID:241294</Xref>
-<Note>chemical and spectrographic characterization; the authors use biochemical rather than IUPAC numbering</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>de Jong, E.</Author>
-<Author>van Berkel, W.J.</Author>
-<Author>van der Zwan, R.P.</Author>
-<Author>de Bont, J.A.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 208, 651-657, 1992</Citation>
-<Title>Purification and characterization of vanillyl-alcohol oxidase from Penicillium simplicissimum. A novel aromatic alcohol oxidase containing covalently bound FAD.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1992.tb17231.x</Xref>
-<Xref>PMID:1396672</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mattevi, A.</Author>
-<Author>Fraaije, M.W.</Author>
-<Author>Mozzarelli, A.</Author>
-<Author>Olivi, L.</Author>
-<Author>Coda, A.</Author>
-<Author>van Berkel, W.J.</Author>
-</Authors>
-<Citation>Structure 5, 907-920, 1997</Citation>
-<Title>Crystal structures and inhibitor binding in the octameric flavoenzyme vanillyl-alcohol oxidase: the shape of the active-site cavity controls substrate specificity.</Title>
-<Xref>DOI:10.1016/S0969-2126(97)00245-1</Xref>
-<Xref>PMID:9261083</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mattevi, A.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, April 1997</Citation>
-<Description>Structure of the octameric flavoenzyme vanillyl-alcohol oxidase.</Description>
-<Xref>PDB:1VAO</Xref>
-<Note>X-ray diffraction, 2.50 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fraaije, M.W.</Author>
-<Author>van den Heuvel, R.H.</Author>
-<Author>van Berkel, W.J.</Author>
-<Author>Mattevi, A.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 274, 35514-35520, 1999</Citation>
-<Title>Covalent flavinylation is essential for efficient redox catalysis in vanillyl-alcohol oxidase.</Title>
-<Xref>DOI:10.1074/jbc.274.50.35514</Xref>
-<Xref>PMID:10585424</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hao, H.X.</Author>
-<Author>Khalimonchuk, O.</Author>
-<Author>Schraders, M.</Author>
-<Author>Dephoure, N.</Author>
-<Author>Bayley, J.P.</Author>
-<Author>Kunst, H.</Author>
-<Author>Devilee, P.</Author>
-<Author>Cremers, C.W.</Author>
-<Author>Schiffman, J.D.</Author>
-<Author>Bentz, B.G.</Author>
-<Author>Gygi, S.P.</Author>
-<Author>Winge, D.R.</Author>
-<Author>Kremer, H.</Author>
-<Author>Rutter, J.</Author>
-</Authors>
-<Citation>Science 325, 1139-1142, 2009</Citation>
-<Title>SDH5, a gene required for flavination of succinate dehydrogenase, is mutated in paraganglioma.</Title>
-<Xref>DOI:10.1126/science.1175689</Xref>
-<Xref>PMID:19628817</Xref>
-<Note>genetic, mutant and interaction analysis in yeast and human; directed mutagenesis in yeast</Note>
-</ReferenceBlock>
-<Comment>The arrangement of the attachment has not been completely established in some cases.</Comment>
-<Comment>The keyword "phosphoprotein" is not used with flavin modifications linked through the flavin.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>apo mitochondrial succinate dehydrogenase [ubiquinone] flavoprotein subunit---FAD ligase sdh5 (EC 6.3.4.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>H</SequenceSpec>
-<Xref>GO:0018297</Xref>
-<Xref>PSI-MOD:00226</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>*phosphoprotein</Keyword>
-<Keyword>FAD</Keyword>
-<Keyword>flavoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__tele-8alpha-fad histidine__h">MOD_RES Tele-8alpha-FAD histidine</Feature>
-</Features>
-<Image src="/images/AA0221.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0221.PDB" />
-</Entry>
-<Entry id="AA0222">
-<Header>
-<Code>AA0222</Code>
-<Dates>
-<CreationDate>10-Nov-1995</CreationDate>
-<StrucRevDate>10-Nov-1995</StrucRevDate>
-<TextChngDate>31-Jul-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>omega-N-phospho-L-arginine</Name>
-<AlternateName>(2S)-2-amino-5-(N'-phosphonocarbamimidamido)pentanoic acid</AlternateName>
-<AlternateName>alpha-amino-delta-phosphonoguanidinovaleric acid</AlternateName>
-<AlternateName>N(gamma)-phosphoarginine</AlternateName>
-<AlternateName>N(omega)-phosphono-L-arginine</AlternateName>
-<AlternateName>N5-[imino(phosphonoamino)methyl]-L-ornithine</AlternateName>
-<AlternateName>phosphoarginine</AlternateName>
-<SystematicName>(2S)-2-amino-5-([amino(phosphonoamino)methylidene]amino)pentanoic acid</SystematicName>
-<Xref>CAS:1189-11-3</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 13 N 4 O 4 P 1</Formula>
-<Weight type="chemical">236.17</Weight>
-<Weight type="physical">236.067442</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0002">
-<Formula>C 0 H 1 N 0 O 3 P 1</Formula>
-<Weight type="chemical">79.98</Weight>
-<Weight type="physical">79.966331</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wakim, B.T.</Author>
-<Author>Aswad, G.D.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 269, 2722-2727, 1994</Citation>
-<Title>Ca(2+)-calmodulin-dependent phosphorylation of arginine in histone 3 by a nuclear kinase from mouse leukemia cells.</Title>
-<Xref>PMID:8300603</Xref>
-<Note>chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fuhrmann, J.</Author>
-<Author>Schmidt, A.</Author>
-<Author>Spiess, S.</Author>
-<Author>Lehner, A.</Author>
-<Author>Turgay, K.</Author>
-<Author>Mechtler, K.</Author>
-<Author>Charpentier, E.</Author>
-<Author>Clausen, T.</Author>
-</Authors>
-<Citation>Science 324, 1323-1327, 2009</Citation>
-<Title>McsB is a protein arginine kinase that phosphorylates and inhibits the heat-shock regulator CtsR.</Title>
-<Xref>DOI:10.1126/science.1170088</Xref>
-<Xref>PMID:19498169</Xref>
-<Note>mass spectrometric and (31)P-NMR identification; in Bacillus stearothermophilus McsB is identified as a protein-arginine kinase acting on CtsR</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>histone-arginine kinase (EC 2.7.3.-)</EnzymeName>
-<EnzymeName>protein-arginine kinase (EC 2.7.3.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>R</SequenceSpec>
-<Xref>GO:0018109</Xref>
-<Xref>PSI-MOD:00227</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__phosphoarginine__r">MOD_RES Phosphoarginine</Feature>
-</Features>
-<Image src="/images/AA0222.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0222.PDB" />
-</Entry>
-<Entry id="AA0223">
-<Header>
-<Code>AA0223</Code>
-<Dates>
-<CreationDate>05-Jan-1996</CreationDate>
-<StrucRevDate>05-Jan-1996</StrucRevDate>
-<TextChngDate>31-Mar-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-(diphytanylglyceryl)-L-cysteine</Name>
-<AlternateName>S-archaeol cysteine</AlternateName>
-<AlternateName>S-[2',3'-bis(phytanyloxy)propyl]cysteine</AlternateName>
-<SystematicName>(2R)-2-amino-3-([(2S)-2,3-bis(3,7,11,15-tetramethylhexadecanyloxy)propyl]sulfanyl)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 46 H 91 N 1 O 3 S 1</Formula>
-<Weight type="chemical">738.30</Weight>
-<Weight type="physical">737.671967</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 43 H 86 N 0 O 2 S 0</Formula>
-<Weight type="chemical">635.16</Weight>
-<Weight type="physical">634.662782</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mattar, S.</Author>
-<Author>Scharf, B.</Author>
-<Author>Kent, S.B.H.</Author>
-<Author>Rodewald, K.</Author>
-<Author>Oesterhelt, D.</Author>
-<Author>Engelhard, M.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 269, 14939-14945, 1994</Citation>
-<Title>The primary structure of halocyanin, an archaeal blue copper protein, predicts a lipid anchor for membrane fixation.</Title>
-<Xref>PMID:8195126</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sagami, H.</Author>
-<Author>Kikuchi, A.</Author>
-<Author>Ogura, K.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 270, 14851-14854, 1995</Citation>
-<Title>A novel type of protein modification by isoprenoid-derived materials. Diphytanylglycerylated proteins in Halobacteria.</Title>
-<Xref>DOI:10.1074/jbc.270.25.14851</Xref>
-<Xref>PMID:7797461</Xref>
-<Note>chromatographic, mass spectrometric and (1)H-NMR identification</Note>
-</ReferenceBlock>
-<Comment>The stereochemistry of the glycerol has not been determined. The S form is shown.</Comment>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Condition>incidental to RESID:AA0043</Condition>
-<Xref>GO:0018115</Xref>
-<Xref>GO:0042050</Xref>
-<Xref>PSI-MOD:00228</Xref>
-<Xref>PSI-MOD:00897</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lipoprotein</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__s-archaeol cysteine__c">LIPID S-archaeol cysteine</Feature>
-</Features>
-<Image src="/images/AA0223.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0223.PDB" />
-</Entry>
-<Entry id="AA0224">
-<Header>
-<Code>AA0224</Code>
-<Dates>
-<CreationDate>26-Jan-1996</CreationDate>
-<StrucRevDate>26-Jan-1996</StrucRevDate>
-<TextChngDate>30-Apr-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>alpha-1-microglobulin-Ig alpha complex chromophore</Name>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 8 N 2 O 2 S 2 +</Formula>
-<Weight type="chemical">204.26 +</Weight>
-<Weight type="physical">204.002720 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005">
-<Formula>C 0 H -2 N 0 O 0 S 0 +</Formula>
-<Weight type="chemical">-2.02 +</Weight>
-<Weight type="physical">-2.015650 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Calero, M.</Author>
-<Author>Escribano, J.</Author>
-<Author>Grubb, A.</Author>
-<Author>Méndez, E.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 269, 384-389, 1994</Citation>
-<Title>Location of a novel type of interpolypeptide chain linkage in the human protein HC-IgA complex (HC-IgA) and identification of a heterogeneous chromophore associated with the complex.</Title>
-<Xref>PMID:7506257</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Åkerström, B.</Author>
-<Author>Bratt, T.</Author>
-<Author>Enghild, J.J.</Author>
-</Authors>
-<Citation>FEBS Lett. 362, 50-54, 1995</Citation>
-<Title>Formation of the α1-microglobulin chromophore in mammalian and insect cells: a novel post-translational mechanism?</Title>
-<Xref>DOI:10.1016/0014-5793(95)00206-O</Xref>
-<Xref>PMID:7535251</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Åkerström, B.</Author>
-<Author>Lögdberg, L.</Author>
-<Author>Berggård, T.</Author>
-<Author>Osmark, P.</Author>
-<Author>Lindqvist, A.</Author>
-</Authors>
-<Citation>Biochim. Biophys. Acta 1482, 172-184, 2000</Citation>
-<Title>α1-Microglobulin: a yellow-brown lipocalin.</Title>
-<Xref>DOI:10.1016/S0167-4838(00)00157-6</Xref>
-<Xref>PMID:11058759</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Allhorn, M.</Author>
-<Author>Berggård, T.</Author>
-<Author>Nordberg, J.</Author>
-<Author>Olsson, M.L.</Author>
-<Author>Åkerström, B.</Author>
-</Authors>
-<Citation>Blood 99, 1894-1901, 2002</Citation>
-<Title>Processing of the lipocalin α1-microglobulin by hemoglobin induces heme-binding and heme-degradation properties.</Title>
-<Xref>DOI:10.1182/blood.V99.6.1894</Xref>
-<Xref>PMID:11877257</Xref>
-</ReferenceBlock>
-<Comment>The structure of the chromophore is not known. It is probably heterogeneous, and involves two cysteines in thioether bonds.</Comment>
-<SequenceCode>
-<SequenceSpec>C, C</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>GO:0019923</Xref>
-<Xref>PSI-MOD:00229</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chromoprotein</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="binding__multimeric 3-hydroxykynurenine chromophore (covalent)__c">BINDING Multimeric 3-hydroxykynurenine chromophore (covalent)</Feature>
-</Features>
-<Image src="/images/AA0224.GIF" alt="DUMMY.GIF" />
-</Entry>
-<Entry id="AA0225">
-<Header>
-<Code>AA0225</Code>
-<Dates>
-<CreationDate>08-Mar-1996</CreationDate>
-<StrucRevDate>16-Jul-1998</StrucRevDate>
-<TextChngDate>20-Apr-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>bis-L-cysteinyl bis-L-histidino diiron disulfide</Name>
-<AlternateName>Rieske iron-sulfur cofactor</AlternateName>
-<SystematicName>di-mu-sulfido(bis-S-cysteinyliron)(bis-N3'-histidinoiron)</SystematicName>
-<Xref>COMe:BIM000056</Xref>
-<Xref>PDBHET:FES</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 18 Fe 2 H 20 N 8 O 4 S 4</Formula>
-<FormalCharge>2-</FormalCharge>
-<Weight type="chemical">652.34</Weight>
-<Weight type="physical">651.920007</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005 AA0009 AA0009">
-<Formula>C 0 Fe 2 H -4 N 0 O 0 S 2</Formula>
-<FormalCharge>2-</FormalCharge>
-<Weight type="chemical">171.78</Weight>
-<Weight type="physical">171.783814</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Rieske, J.S.</Author>
-<Author>MacLennan, D.H.</Author>
-<Author>Coleman, R.</Author>
-</Authors>
-<Citation>Biochem. Biophys. Res. Commun. 15, 338-344, 1964</Citation>
-<Title>Isolation and properties of an iron-protein from the (reduced coenzyme Q)-cytochrome C reductase complex of the respiratory chain.</Title>
-<Xref>DOI:10.1016/0006-291X(64)90171-8</Xref>
-<Note>elemental analysis; EPR spectrometry</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gurbiel, R.J.</Author>
-<Author>Batie, C.J.</Author>
-<Author>Sivaraja, M.</Author>
-<Author>True, A.E.</Author>
-<Author>Fee, J.A.</Author>
-<Author>Hoffman, B.M.</Author>
-<Author>Ballou, D.P.</Author>
-</Authors>
-<Citation>Biochemistry 28, 4861-4871, 1989</Citation>
-<Title>Electron-nuclear double resonance spectroscopy of (15)N-enriched phthalate dioxygenase from Pseudomonas cepacia proves that two histidines are coordinated to the [2Fe-2S] Rieske-type clusters.</Title>
-<Xref>DOI:10.1021/bi00437a051</Xref>
-<Xref>PMID:2765515</Xref>
-<Note>(15)N-NMR characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Iwata, S.</Author>
-<Author>Saynovits, M.</Author>
-<Author>Link, T.A.</Author>
-<Author>Michel, H.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, February 1996</Citation>
-<Description>Structure of a water soluble fragment of the Rieske iron-sulfur protein of the bovine heart mitochondrial cytochrome bc1-complex.</Description>
-<Xref>PDB:1RIE</Xref>
-<Note>X-ray diffraction, 1.5 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Iwata, S.</Author>
-<Author>Lee, J.W.</Author>
-<Author>Okada, K.</Author>
-<Author>Lee, J.K.</Author>
-<Author>Iwata, M.</Author>
-<Author>Rasmussen, B.</Author>
-<Author>Link, T.A.</Author>
-<Author>Ramaswamy, S.</Author>
-<Author>Jap, B.K.</Author>
-</Authors>
-<Citation>Science 281, 64-71, 1998</Citation>
-<Title>Complete structure of the 11-subunit bovine mitochondrial cytochrome bc1 complex.</Title>
-<Xref>DOI:10.1126/science.281.5373.64</Xref>
-<Xref>PMID:9651245</Xref>
-<Note>X-ray diffraction, 4.0 angstroms</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>C, C, H, H</SequenceSpec>
-<Condition>cross-link 4</Condition>
-<Xref>GO:0018299</Xref>
-<Xref>PSI-MOD:00230</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>2Fe-2S</Keyword>
-<Keyword>metalloprotein</Keyword>
-<Keyword>Rieske iron-sulfur protein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="metal__iron-sulfur (2fe-2s)__c">METAL Iron-sulfur (2Fe-2S)</Feature>
-<Feature type="UniProt" key="metal__iron-sulfur (2fe-2s); via pros nitrogen__h">METAL Iron-sulfur (2Fe-2S); via pros nitrogen</Feature>
-</Features>
-<Image src="/images/AA0225.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0225.PDB" />
-</Entry>
-<Entry id="AA0226">
-<Header>
-<Code>AA0226</Code>
-<Dates>
-<CreationDate>08-Mar-1996</CreationDate>
-<StrucRevDate>08-Mar-1996</StrucRevDate>
-<TextChngDate>01-Mar-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>hexakis-L-cysteinyl hexairon hexasulfide</Name>
-<AlternateName>hexa-mu3-sulfido-hexakis(S-cysteinyliron)</AlternateName>
-<AlternateName>prismane iron-sulfur cofactor</AlternateName>
-<SystematicName>hexa-mu3-sulfido-hexakis(cysteinato-kappaS)-hexairon</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 18 Fe 6 H 24 N 6 O 6 S 12</Formula>
-<FormalCharge>1-</FormalCharge>
-<Weight type="chemical">1140.22</Weight>
-<Weight type="physical">1139.450758</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005 AA0005 AA0005 AA0005 AA0005">
-<Formula>C 0 Fe 6 H -6 N 0 O 0 S 6</Formula>
-<FormalCharge>1-</FormalCharge>
-<Weight type="chemical">521.38</Weight>
-<Weight type="physical">521.395649</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Moura, I.</Author>
-<Author>Tavares, P.</Author>
-<Author>Moura, J.J.</Author>
-<Author>Ravi, N.</Author>
-<Author>Huynh, B.H.</Author>
-<Author>Liu, M.Y.</Author>
-<Author>LeGall, J.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 267, 4489-4496, 1992</Citation>
-<Title>Direct spectroscopic evidence for the presence of a 6Fe cluster in an iron-sulfur protein isolated from Desulfovibrio desulfuricans (ATCC 27774).</Title>
-<Xref>PMID:1311311</Xref>
-<Note>EPR and Moessbauer spectrographic analysis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Pierik, A.J.</Author>
-<Author>Hagen, W.R.</Author>
-<Author>Dunham, W.R.</Author>
-<Author>Sands, R.H.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 206, 705-719, 1992</Citation>
-<Title>Multi-frequency EPR and high-resolution Mössbauer spectroscopy of a putative [6Fe-6S] prismane-cluster-containing protein from Desulfovibrio vulgaris (Hildenborough).</Title>
-<Xref>DOI:10.1111/j.1432-1033.1992.tb16977.x</Xref>
-<Xref>PMID:1318833</Xref>
-<Note>EPR and Moessbauer spectrographic analysis</Note>
-</ReferenceBlock>
-<Comment>The prismane 6Fe-6S cluster is now thought not to exist. The structure determined by X-ray consists of a 4Fe-4S cluster, see RESID:AA0140, and a four iron cluster with mixed ligands, see RESID:AA0268.</Comment>
-<Comment>The formal charge for the hypothetical "as-isolated" ligated cluster was 1-.</Comment>
-<SequenceCode>
-<SequenceSpec>C, C, C, C, C, C</SequenceSpec>
-<Condition>cross-link 6</Condition>
-<Xref>GO:0018300</Xref>
-<Xref>PSI-MOD:00231</Xref>
-</SequenceCode>
-<Source>deprecated</Source>
-<Keywords>
-<Keyword>iron-sulfur protein</Keyword>
-<Keyword>metalloprotein</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this dubious modification is not currently annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0226.GIF" alt="DUMMY.GIF" />
-</Entry>
-<Entry id="AA0227">
-<Header>
-<Code>AA0227</Code>
-<Dates>
-<CreationDate>17-May-1996</CreationDate>
-<StrucRevDate>17-May-1996</StrucRevDate>
-<TextChngDate>31-Dec-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6-(phospho-5'-adenosine)-L-lysine</Name>
-<AlternateName>5'-adenylic-N6-L-lysine</AlternateName>
-<AlternateName>epsilon-5'-adenylic-L-lysine</AlternateName>
-<AlternateName>L-lysine monoanhydride with 5'-adenylic acid</AlternateName>
-<AlternateName>N(zeta)-5'-adenylic-L-lysine</AlternateName>
-<AlternateName>N6-L-lysine 5'-adenosine phosphoramidester</AlternateName>
-<SystematicName>(2S)-2-amino-6-(5'-adenosine phosphonamino)hexanoic acid</SystematicName>
-<Xref>CAS:35985-27-4</Xref>
-<Xref>PDBHET:AMP</Xref>
-<Xref>PDBHET:APK</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 16 H 24 N 7 O 7 P 1</Formula>
-<Weight type="chemical">457.38</Weight>
-<Weight type="physical">457.147483</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 10 H 12 N 5 O 6 P 1</Formula>
-<Weight type="chemical">329.21</Weight>
-<Weight type="physical">329.052520</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gumport, R.I.</Author>
-<Author>Lehman, I.R.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 68, 2559-2563, 1971</Citation>
-<Title>Structure of the DNA ligase-adenylate intermediate: lysine (epsilon-amino)-linked adenosine monophosphoramidate.</Title>
-<Xref>DOI:10.1073/pnas.68.10.2559</Xref>
-<Xref>PMID:4944632</Xref>
-<Note>chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Thogersen, H.C.</Author>
-<Author>Morris, H.R.</Author>
-<Author>Rand, K.N.</Author>
-<Author>Gait, M.J.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 147, 325-329, 1985</Citation>
-<Title>Location of the adenylylation site in T4 RNA ligase.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1985.tb08753.x</Xref>
-<Xref>PMID:3882425</Xref>
-<Note>mass spectrometric characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Cotner-Gohara, E.</Author>
-<Author>Kim, I.-K.</Author>
-<Author>Hammel, M.</Author>
-<Author>Tainer, J.A.</Author>
-<Author>Tomkinson, A.E.</Author>
-<Author>Ellenberger, T.</Author>
-</Authors>
-<Citation>Biochemistry 49, 6165-6176, 2010</Citation>
-<Title>Human DNA ligase III recognizes DNA ends by dynamic switching between two DNA-bound states.</Title>
-<Xref>DOI:10.1021/bi100503w</Xref>
-<Xref>PMID:20518483</Xref>
-<Note>X-ray diffraction, 3.00 angstroms; authors' initials in the PubMed citation are corrected</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Cotner-Gohara, E.</Author>
-<Author>Kim, I.-K.</Author>
-<Author>Hammel, M.</Author>
-<Author>Tainer, J.A.</Author>
-<Author>Tomkinson, A.E.</Author>
-<Author>Ellenberger, T.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, December 2009</Citation>
-<Description>Human DNA ligase III recognizes DNA ends by dynamic switching between two DNA bound states.</Description>
-<Xref>PDB:3L2P</Xref>
-<Note>X-ray diffraction, 3.00 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hansen, T.</Author>
-<Author>Albers, M.</Author>
-<Author>Hedberg, C.</Author>
-<Author>Sickmann, A.</Author>
-</Authors>
-<Citation>Proteomics 13, 955-963, 2013</Citation>
-<Title>Adenylylation, MS, and proteomics --- Introducing a "new" modification to bottom-up proteomics.</Title>
-<Xref>DOI:10.1002/pmic.201200344</Xref>
-<Xref>PMID:23335384</Xref>
-<Note>mass spectrometric detection; analysis comparison; confirms that phosphodiester modifications, such as adenylylation, can be incorrectly identified as phosphorylations in some experiments</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>GO:0018116</Xref>
-<Xref>GO:0018329</Xref>
-<Xref>PSI-MOD:00232</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="act_site__n6-amp-lysine intermediate__k">ACT_SITE N6-AMP-lysine intermediate</Feature>
-</Features>
-<Image src="/images/AA0227.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0227.PDB" />
-</Entry>
-<Entry id="AA0228">
-<Header>
-<Code>AA0228</Code>
-<Dates>
-<CreationDate>17-May-1996</CreationDate>
-<StrucRevDate>17-May-1996</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6-(phospho-5'-guanosine)-L-lysine</Name>
-<AlternateName>5'-guanylic-N6-L-lysine</AlternateName>
-<AlternateName>epsilon-5'-guanylic-L-lysine</AlternateName>
-<AlternateName>L-lysine monoanhydride with 5'-guanylic acid</AlternateName>
-<AlternateName>lysine guanosine-5'-monophosphate</AlternateName>
-<AlternateName>N(zeta)-5'-guanylic-lysine</AlternateName>
-<AlternateName>N6-(5'-guanylyl)-lysine </AlternateName>
-<AlternateName>N6-L-lysine 5'-guanosine phosphoramidester</AlternateName>
-<SystematicName>(2S)-2-amino-6-(5'-guanosine phosphonamino)hexanoic acid</SystematicName>
-<Xref>ChEBI:138294</Xref>
-<Xref>PDBHET:GPL</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 16 H 24 N 7 O 8 P 1</Formula>
-<Weight type="chemical">473.38</Weight>
-<Weight type="physical">473.142397</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 10 H 12 N 5 O 7 P 1</Formula>
-<Weight type="chemical">345.21</Weight>
-<Weight type="physical">345.047434</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Shuman, S.</Author>
-<Author>Hurwitz, J.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 78, 187-191, 1981</Citation>
-<Title>Mechanism of mRNA capping by vaccinia virus guanylyltransferase: characterization of an enzyme-guanylate intermediate.</Title>
-<Xref>DOI:10.1073/pnas.78.1.187</Xref>
-<Xref>PMID:6264433</Xref>
-<Note>chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Roth, M.J.</Author>
-<Author>Hurwitz, J.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 259, 13488-13494, 1984</Citation>
-<Title>RNA capping by the vaccinia virus guanylyltransferase. Structure of enzyme-guanylate intermediate.</Title>
-<Xref>PMID:6092377</Xref>
-<Note>chemical characterization</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>GO:0018261</Xref>
-<Xref>GO:0018330</Xref>
-<Xref>PSI-MOD:00233</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="act_site__n6-gmp-lysine intermediate__k">ACT_SITE N6-GMP-lysine intermediate</Feature>
-</Features>
-<Image src="/images/AA0228.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0228.PDB" />
-</Entry>
-<Entry id="AA0229">
-<Header>
-<Code>AA0229</Code>
-<Dates>
-<CreationDate>17-May-1996</CreationDate>
-<StrucRevDate>17-May-1996</StrucRevDate>
-<TextChngDate>13-Sep-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-cysteine glutathione disulfide</Name>
-<AlternateName>cysteinyl glutathione</AlternateName>
-<AlternateName>L-gamma-glutamyl-L-cysteinyl-glycine (2-1')-disulfide with L-cysteine</AlternateName>
-<AlternateName>N-(N-gamma-glutamyl-cystinyl)-glycine</AlternateName>
-<SystematicName>(2S)-2-amino-3-((2S)-2-((4R)-4-amino-4-carboxyl-1-oxobutyl)amino-3-(carboxylmethyl)amino-3-oxo-propyl)dithio-propanoic acid</SystematicName>
-<Xref>CAS:13081-14-6</Xref>
-<Xref>ChEBI:21264</Xref>
-<Xref>PDBHET:GSH</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 13 H 20 N 4 O 7 S 2</Formula>
-<Weight type="chemical">408.44</Weight>
-<Weight type="physical">408.077341</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 10 H 15 N 3 O 6 S 1</Formula>
-<Weight type="chemical">305.30</Weight>
-<Weight type="physical">305.068156</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bergenhem, N.</Author>
-<Author>Carlsson, U.</Author>
-<Author>Strid, L.</Author>
-</Authors>
-<Citation>Biochim. Biophys. Acta 871, 55-60, 1986</Citation>
-<Title>The existence of glutathione and cysteine disulfide-linked to erythrocyte carbonic anhydrase from tiger shark.</Title>
-<Xref>DOI:10.1016/0167-4838(86)90132-9</Xref>
-<Xref>PMID:3083866</Xref>
-<Note>chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Dörmann, P.</Author>
-<Author>Börchers, T.</Author>
-<Author>Korf, U.</Author>
-<Author>Højrup, P.</Author>
-<Author>Roepstorff, P.</Author>
-<Author>Spener, F.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 268, 16286-16292, 1993</Citation>
-<Title>Amino acid exchange and covalent modification by cysteine and glutathione explain isoforms of fatty acid-binding protein occurring in bovine liver.</Title>
-<Xref>PMID:8344916</Xref>
-<Note>chemical characterization</Note>
-</ReferenceBlock>
-<Comment>Disulfide formation with free glutatione extracellularly is probably not enzymatically catalyzed.</Comment>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>GO:0018118</Xref>
-<Xref>PSI-MOD:00234</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>disulfide bond</Keyword>
-<Keyword>glutathione</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__s-glutathionyl cysteine__c">MOD_RES S-glutathionyl cysteine</Feature>
-</Features>
-<Image src="/images/AA0229.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0229.PDB" />
-</Entry>
-<Entry id="AA0230">
-<Header>
-<Code>AA0230</Code>
-<Dates>
-<CreationDate>17-May-1996</CreationDate>
-<StrucRevDate>17-May-1996</StrucRevDate>
-<TextChngDate>01-Mar-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-nitrosyl-L-cysteine</Name>
-<AlternateName>L-cysteine nitrite ester</AlternateName>
-<AlternateName>S-nitrosocysteine</AlternateName>
-<SystematicName>(2R)-2-amino-3-nitrososulfanyl-propanoic acid</SystematicName>
-<Xref>CAS:51209-75-7</Xref>
-<Xref>PDBHET:NO</Xref>
-<Xref>PDBHET:SNC</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 4 N 2 O 2 S 1</Formula>
-<Weight type="chemical">132.14</Weight>
-<Weight type="physical">131.999348</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 0 H -1 N 1 O 1 S 0</Formula>
-<Weight type="chemical">29.00</Weight>
-<Weight type="physical">28.990164</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Jia, L.</Author>
-<Author>Bonaventura, C.</Author>
-<Author>Bonaventura, J.</Author>
-<Author>Stamler, J.S.</Author>
-</Authors>
-<Citation>Nature 380, 221-226, 1996</Citation>
-<Title>S-Nitrosohaemoglobin: a dynamic activity of blood involved in vascular control.</Title>
-<Xref>DOI:10.1038/380221a0</Xref>
-<Xref>PMID:8637569</Xref>
-<Note>evidence is presented for the binding of nitrosonium to form S-nitrosocysteine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mohr, S.</Author>
-<Author>Stamler, J.S.</Author>
-<Author>Bruene, B.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 271, 4209-4214, 1996</Citation>
-<Title>Posttranslational modification of glyceraldehyde-3-phosphate dehydrogenase by S-nitrosylation and subsequent NADH attachment.</Title>
-<Xref>DOI:10.1074/jbc.271.8.4209</Xref>
-<Xref>PMID:8626764</Xref>
-<Note>chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Chan, N.L.</Author>
-<Author>Rogers, P.H.</Author>
-<Author>Arnone, A.</Author>
-</Authors>
-<Citation>Biochemistry 37, 16459-16464, 1998</Citation>
-<Title>Crystal structure of the S-nitroso form of liganded human hemoglobin.</Title>
-<Xref>DOI:10.1021/bi9816711</Xref>
-<Xref>PMID:9843411</Xref>
-<Note>X-ray diffraction, 1.8 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sun, J.H.</Author>
-<Author>Xin, C.L.</Author>
-<Author>Eu, J.P.</Author>
-<Author>Stamler, J.S.</Author>
-<Author>Meissner, G.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 98, 11158-11162, 2001</Citation>
-<Title>Cysteine-3635 is responsible for skeletal muscle ryanodine receptor modulation by NO.</Title>
-<Xref>DOI:10.1073/pnas.201289098</Xref>
-<Xref>PMID:11562475</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Doulias, P.T.</Author>
-<Author>Greene, J.L.</Author>
-<Author>Greco, T.M.</Author>
-<Author>Tenopoulou, M.</Author>
-<Author>Seeholzer, S.H.</Author>
-<Author>Dunbrack, R.L.</Author>
-<Author>Ischiropoulos, H.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 107, 16958-16963, 2010</Citation>
-<Title>Structural profiling of endogenous S-nitrosocysteine residues reveals unique features that accommodate diverse mechanisms for protein S-nitrosylation.</Title>
-<Xref>DOI:10.1073/pnas.1008036107</Xref>
-<Xref>PMID:20837516</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kornberg, M.D.</Author>
-<Author>Sen, N.</Author>
-<Author>Hara, M.R.</Author>
-<Author>Juluri, K.R.</Author>
-<Author>Nguyen, J.V.</Author>
-<Author>Snowman, A.M.</Author>
-<Author>Law, L.</Author>
-<Author>Hester, L.D.</Author>
-<Author>Snyder, S.H.</Author>
-</Authors>
-<Citation>Nature Cell Biol. 12, 1094-1100, 2010</Citation>
-<Title>GAPDH mediates nitrosylation of nuclear proteins.</Title>
-<Xref>DOI:10.1038/ncb2114</Xref>
-<Xref>PMID:20972425</Xref>
-<Note>S-nitrosylated glyceraldehyde-3-phosphate dehydrogenase can transfer the nitrosyl group to cysteine residues of other proteins, acting as a carrier protein</Note>
-</ReferenceBlock>
-<Comment>The reaction of nitrosonium (NO+) with cysteine residues may not be enzymatically catalyzed; the reaction of a cysteine residue with, or the reductive production of, nitric oxide (NO) has not been clarified.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-<EnzymeName>peptidyl-cysteine S-nitrosyltransferase (EC 2.6.99.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>GO:0018119</Xref>
-<Xref>PSI-MOD:00235</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="mod_res__s-nitrosocysteine__c">MOD_RES S-nitrosocysteine</Feature>
-</Features>
-<Image src="/images/AA0230.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0230.PDB" />
-</Entry>
-<Entry id="AA0231">
-<Header>
-<Code>AA0231</Code>
-<Dates>
-<CreationDate>24-May-1996</CreationDate>
-<StrucRevDate>24-May-1996</StrucRevDate>
-<TextChngDate>30-Sep-2008</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N4-(ADP-ribosyl)-L-asparagine</Name>
-<AlternateName>N4-alpha-D-ribofuranosyl-L-asparagine 5'-&gt;5'-ester with adenosine 5'-(trihydrogen diphosphate)</AlternateName>
-<AlternateName>N4-[alpha-D-ribofuranoside 5'-&gt;5'-ester with adenosine 5'-(trihydrogen diphosphate)]-L-asparagine</AlternateName>
-<SystematicName>(S)-2-amino-4-([adenosine 5'-(trihydrogen diphosphate) 5'-&gt;5'-ester with alpha-D-ribofuranosyl]amino)-4-oxobutanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 19 H 27 N 7 O 15 P 2</Formula>
-<Weight type="chemical">655.41</Weight>
-<Weight type="physical">655.104036</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0003">
-<Formula>C 15 H 21 N 5 O 13 P 2</Formula>
-<Weight type="chemical">541.30</Weight>
-<Weight type="physical">541.061109</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sekine, A.</Author>
-<Author>Fujiwara, M.</Author>
-<Author>Narumiya, S.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 264, 8602-8605, 1989</Citation>
-<Title>Asparagine residue in the rho gene product is the modification site for botulinum ADP-ribosyltransferase.</Title>
-<Xref>PMID:2498316</Xref>
-<Note>identification of ADP-ribosylation site</Note>
-</ReferenceBlock>
-<Comment>It is not known whether botulinum exoenzyme C3 catalyzes formation of the alpha or beta isomer. The alpha form is presented.</Comment>
-<Comment>The keyword "phosphoprotein" is not used with toxin modification.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>NAD(P)+--asparagine ADP-ribosyltransferase (EC 2.4.2.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>N</SequenceSpec>
-<Xref>GO:0006471</Xref>
-<Xref>GO:0018122</Xref>
-<Xref>PSI-MOD:00236</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>*phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__adp-ribosylasparagine__n">MOD_RES ADP-ribosylasparagine</Feature>
-</Features>
-<Image src="/images/AA0231.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0231.PDB" />
-</Entry>
-<Entry id="AA0232">
-<Header>
-<Code>AA0232</Code>
-<Dates>
-<CreationDate>16-Aug-1996</CreationDate>
-<StrucRevDate>30-Sep-2009</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>3-(methylthio)-L-aspartic acid</Name>
-<AlternateName>3-carboxy-S-methyl-cysteine</AlternateName>
-<AlternateName>3-methylthio-aspartic acid</AlternateName>
-<AlternateName>beta-methylthio-aspartic acid</AlternateName>
-<SystematicName>(2R,3Xi)-2-amino-3-(methylsulfanyl)butanedioic acid</SystematicName>
-<Xref>CAS:180420-54-6</Xref>
-<Xref>ChEBI:73619</Xref>
-<Xref>PDBHET:OTD</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 7 N 1 O 3 S 1</Formula>
-<Weight type="chemical">161.18</Weight>
-<Weight type="physical">161.014664</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0004">
-<Formula>C 1 H 2 N 0 O 0 S 1</Formula>
-<Weight type="chemical">46.09</Weight>
-<Weight type="physical">45.987721</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kowalak, J.A.</Author>
-<Author>Walsh, K.A.</Author>
-</Authors>
-<Citation>Protein Sci. 5, 1625-1632, 1996</Citation>
-<Title>beta-Methylthio-aspartic acid: Identification of a novel posttranslational modification in ribosomal protein S12 from Escherichia coli.</Title>
-<Xref>DOI:10.1002/pro.5560050816</Xref>
-<Xref>PMID:8844851</Xref>
-<Note>mass spectrometric identification; chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Strader, M.B.</Author>
-<Author>VerBerkmoes, N.C.</Author>
-<Author>Tabb, D.L.</Author>
-<Author>Connelly, H.M.</Author>
-<Author>Barton, J.W.</Author>
-<Author>Bruce, B.D.</Author>
-<Author>Pelletier, D.A.</Author>
-<Author>Davison, B.H.</Author>
-<Author>Hettich, R.L.</Author>
-<Author>Larimer, F.W.</Author>
-<Author>Hurst, G.B.</Author>
-</Authors>
-<Citation>J. Proteome Res. 3, 965-978, 2004</Citation>
-<Title>Characterization of the 70S Ribosome from Rhodopseudomonas palustris Using an Integrated "Top-Down" and "Bottom-Up" Mass Spectrometric Approach.</Title>
-<Xref>DOI:10.1021/pr049940z</Xref>
-<Xref>PMID:15473684</Xref>
-<Note>the capitalization of "Verberkmoes" in the PubMed citation is corrected</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Anton, B.P.</Author>
-<Author>Saleh, L.</Author>
-<Author>Benner, J.S.</Author>
-<Author>Raleigh, E.A.</Author>
-<Author>Kasif, S.</Author>
-<Author>Roberts, R.J.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 105, 1826-1831, 2008</Citation>
-<Title>RimO, a MiaB-like enzyme, methylthiolates the universally conserved Asp88 residue of ribosomal protein S12 in Escherichia coli.</Title>
-<Xref>DOI:10.1073/pnas.0708608105</Xref>
-<Xref>PMID:18252828</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Demirci, H.</Author>
-<Author>Murphy IV, F.</Author>
-<Author>Murphy, E.</Author>
-<Author>Gregory, S.T.</Author>
-<Author>Dahlberg, A.E.</Author>
-<Author>Jogl, G.</Author>
-</Authors>
-<Citation>Nature Commun. 4, 1355, 2013</Citation>
-<Title>A structural basis for streptomycin-induced misreading of the genetic code.</Title>
-<Xref>DOI:10.1038/ncomms2346</Xref>
-<Xref>PMID:23322043</Xref>
-<Note>X-ray diffraction, 3.60 angstroms; a structure was built incorporating the (2R,3S) model; the suffix of F. Murphy IV in the PubMed citation is corrected</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Demirci, H.</Author>
-<Author>Murphy IV, F.</Author>
-<Author>Murphy, E.</Author>
-<Author>Gregory, S.T.</Author>
-<Author>Dahlberg, A.E.</Author>
-<Author>Jogl, G.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, February 2012</Citation>
-<Description>Crystal structure of the apo 30s ribosomal subunit from Thermus thermophilus (HB8).</Description>
-<Xref>PDB:4DR1</Xref>
-<Note>X-ray diffraction, 3.60 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Arragain, S.</Author>
-<Author>Garcia-Serres, R.</Author>
-<Author>Blondin, G.</Author>
-<Author>Douki, T.</Author>
-<Author>Clemancey, M.</Author>
-<Author>Latour, J.M.</Author>
-<Author>Forouhar, F.</Author>
-<Author>Neely, H.</Author>
-<Author>Montelione, G.T.</Author>
-<Author>Hunt, J.F.</Author>
-<Author>Mulliez, E.</Author>
-<Author>Fontecave, M.</Author>
-<Author>Atta, M.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 285, 5792-5801, 2010</Citation>
-<Title>Post-translational modification of ribosomal proteins: structural and functional characterization of RimO from Thermotoga maritima, a radical S-adenosylmethionine methylthiotransferase.</Title>
-<Xref>DOI:10.1074/jbc.M109.065516</Xref>
-<Xref>PMID:20007320</Xref>
-<Note>the modification enzyme contains a [4Fe-4S-AdoMet] radical-SAM cluster and an additional [4Fe-4S] cluster with 3 cysteine ligands; double modification can occur with the model substrate</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Forouhar, F.</Author>
-<Author>Arragain, S.</Author>
-<Author>Atta, M.</Author>
-<Author>Gambarelli, S.</Author>
-<Author>Mouesca, J.M.</Author>
-<Author>Hussain, M.</Author>
-<Author>Xiao, R.</Author>
-<Author>Kieffer-Jaquinod, S.</Author>
-<Author>Seetharaman, J.</Author>
-<Author>Acton, T.B.</Author>
-<Author>Montelione, G.T.</Author>
-<Author>Mulliez, E.</Author>
-<Author>Hunt, J.F.</Author>
-<Author>Fontecave, M.</Author>
-</Authors>
-<Citation>Nature Chem. Biol. 9, 333-338, 2013</Citation>
-<Title>Two Fe-S clusters catalyze sulfur insertion by radical-SAM methylthiotransferases.</Title>
-<Xref>DOI:10.1038/nchembio.1229</Xref>
-<Xref>PMID:23542644</Xref>
-<Note>enzymatic mechanism of modification; the enzyme contains 3 to 5 additional exogenous sulfur atoms connecting the iron-sulfur clusters; evidence that first a hydrogen radical is abstracted, a sulfur atom is inserted, then a methyl radical is transferred; double modification can occur with a model substrate</Note>
-</ReferenceBlock>
-<Comment>The stereochemistry for the second chiral center has not been resolved. The (2R,3S) form is shown.</Comment>
-<Comment>beta-Methylthioaspartic acid probably occurs uniquely in ribosomal protein S12. Althouh the aspartic acid is invariant, the modification is not required for activity.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>ribosomal protein S12 methylthiotransferase RimO (EC 2.-.-.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>D</SequenceSpec>
-<Xref>GO:0018339</Xref>
-<Xref>PSI-MOD:00237</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__3-methylthioaspartic acid__d">MOD_RES 3-methylthioaspartic acid</Feature>
-</Features>
-<Image src="/images/AA0232.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0232.PDB" />
-</Entry>
-<Entry id="AA0233">
-<Header>
-<Code>AA0233</Code>
-<Dates>
-<CreationDate>06-Sep-1996</CreationDate>
-<StrucRevDate>06-Sep-1996</StrucRevDate>
-<TextChngDate>31-Jul-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>2'-(L-lys-N6-yl)-L-4',5'-topaquinone</Name>
-<AlternateName>2'-(L-lysine)-L-tyrosyl-4',5'-quinone</AlternateName>
-<AlternateName>LTQ</AlternateName>
-<AlternateName>lysyl oxidase cofactor</AlternateName>
-<SystematicName>1-[(S)-5-amino-5-carboxypentyl]amino-2-[(S)-2-amino-2-carboxyethyl]-2,6-cyclohexadien-4,5-dione</SystematicName>
-<Xref>COMe:BIM000263</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 15 H 17 N 3 O 4</Formula>
-<Weight type="chemical">303.32</Weight>
-<Weight type="physical">303.121906</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012 AA0019">
-<Formula>C 0 H -4 N 0 O 1</Formula>
-<Weight type="chemical">11.97</Weight>
-<Weight type="physical">11.963614</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wang, S.X.</Author>
-<Author>Mure, M.</Author>
-<Author>Medzihradszky, K.F.</Author>
-<Author>Burlingame, A.L.</Author>
-<Author>Brown, D.E.</Author>
-<Author>Dooley, D.M.</Author>
-<Author>Smith, A.J.</Author>
-<Author>Kagan, H.M.</Author>
-<Author>Klinman, J.P.</Author>
-</Authors>
-<Citation>Science 273, 1078-1084, 1996</Citation>
-<Title>A crosslinked cofactor in lysyl oxidase: redox function for amino acid side chains.</Title>
-<Xref>DOI:10.1126/science.273.5278.1078</Xref>
-<Xref>PMID:8688089</Xref>
-<Note>mass spectrometric, raman spectrographic, visible/UV spectrographic, and chemical characterization; phenylhydrazine derivative</Note>
-</ReferenceBlock>
-<Comment>The linkage between the two components has not been established with certainty. The relation of this cofactor to the copper binding site has not been established.</Comment>
-<SequenceCode>
-<SequenceSpec>K, Y</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Condition>secondary to RESID:AA0147</Condition>
-<Xref>GO:0018124</Xref>
-<Xref>PSI-MOD:00238</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>quinoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__lysine tyrosylquinone (lys-tyr)__k__y">CROSSLNK Lysine tyrosylquinone (Lys-Tyr)</Feature>
-<Feature type="UniProt" key="crosslnk__lysine tyrosylquinone (tyr-lys)__y__k">CROSSLNK Lysine tyrosylquinone (Tyr-Lys)</Feature>
-</Features>
-<Image src="/images/AA0233.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0233.PDB" />
-</Entry>
-<Entry id="AA0234">
-<Header>
-<Code>AA0234</Code>
-<Dates>
-<CreationDate>06-Sep-1996</CreationDate>
-<StrucRevDate>06-Sep-1996</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-methyl-L-cysteine</Name>
-<AlternateName>L-3-(methylthio)alanine</AlternateName>
-<SystematicName>(R)-2-amino-3-(methylsulfanyl)propanoic acid</SystematicName>
-<Xref>CAS:1187-84-4</Xref>
-<Xref>ChEBI:82612</Xref>
-<Xref>PDBHET:SMC</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 7 N 1 O 1 S 1</Formula>
-<Weight type="chemical">117.17</Weight>
-<Weight type="physical">117.024835</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 1 H 2 N 0 O 0 S 0</Formula>
-<Weight type="chemical">14.03</Weight>
-<Weight type="physical">14.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gonzalez, J.C.</Author>
-<Author>Banerjee, R.V.</Author>
-<Author>Huang, S.</Author>
-<Author>Sumner, J.S.</Author>
-<Author>Matthews, R.G.</Author>
-</Authors>
-<Citation>Biochemistry 31, 6045-6056, 1992</Citation>
-<Title>Comparison of cobalamin-independent and cobalamin-dependent methionine synthases from Escherichia coli: two solutions to the same chemical problem.</Title>
-<Xref>DOI:10.1021/bi00141a013</Xref>
-<Xref>PMID:1339288</Xref>
-<Note>radioisotope labeling</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Selmer, T.</Author>
-<Author>Kahnt, J.</Author>
-<Author>Goubeaud, M.</Author>
-<Author>Shima, S.</Author>
-<Author>Grabarse, W.</Author>
-<Author>Ermler, U.</Author>
-<Author>Thauer, R.K.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 275, 3755-3760, 2000</Citation>
-<Title>The biosynthesis of methylated amino acids in the active site region of methyl-coenzyme M reductase.</Title>
-<Xref>DOI:10.1074/jbc.275.6.3755</Xref>
-<Xref>PMID:10660523</Xref>
-<Note>mass spectrometric characterization; in methyl-coenzyme M reductase the biosynthetic origin of the methyl group is S-adenosyl methionine, not methyl-coenzyme M</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Taylor, T.C.</Author>
-<Author>Backlund, A.</Author>
-<Author>Bjorhall, K.</Author>
-<Author>Spreitzer, R.J.</Author>
-<Author>Andersson, I.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 276, 48159-48164, 2001</Citation>
-<Title>First crystal structure of Rubisco from a green alga, Chlamydomonas reinhardtii.</Title>
-<Xref>DOI:10.1074/jbc.M107765200</Xref>
-<Xref>PMID:11641402</Xref>
-<Note>X-ray diffraction, 1.40 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Taylor, T.C.</Author>
-<Author>Spreitzer, R.J.</Author>
-<Author>Andersson, I.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, August 2001</Citation>
-<Description>Rubisco from Chlamydomonas reinhardtii.</Description>
-<Xref>PDB:1GK8</Xref>
-<Note>X-ray diffraction, 1.40 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Grove, T.L.</Author>
-<Author>Benner, J.S.</Author>
-<Author>Radle, M.I.</Author>
-<Author>Ahlum, J.H.</Author>
-<Author>Landgraf, B.J.</Author>
-<Author>Krebs, C.</Author>
-<Author>Booker, S.J.</Author>
-</Authors>
-<Citation>Science 332, 604-607, 2011</Citation>
-<Title>A radically different mechanism for S-adenosylmethionine-dependent methyltransferases.</Title>
-<Xref>DOI:10.1126/science.1200877</Xref>
-<Xref>PMID:21415317</Xref>
-<Note>isotope labeling mass spectrometric detection</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Boal, A.K.</Author>
-<Author>Grove, T.L.</Author>
-<Author>McLaughlin, M.I.</Author>
-<Author>Yennawar, N.H.</Author>
-<Author>Booker, S.J.</Author>
-<Author>Rosenzweig, A.C.</Author>
-</Authors>
-<Citation>Science 332, 1089-1092, 2011</Citation>
-<Title>Structural basis for methyl transfer by a radical SAM enzyme.</Title>
-<Xref>DOI:10.1126/science.1205358</Xref>
-<Xref>PMID:21527678</Xref>
-<Note>X-ray diffraction, 2.05 angstroms; an S-methylcysteine is generated in the enzyme, converted to a radical, and transfered as a methyl radical</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Boal, A.K.</Author>
-<Author>Grove, T.L.</Author>
-<Author>McLaughlin, M.I.</Author>
-<Author>Yennawar, N.H.</Author>
-<Author>Booker, S.J.</Author>
-<Author>Rosenzweig, A.C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, April 2005</Citation>
-<Description>X-ray structure of RlmN from Escherichia coli in complex with S-adenosylmethionine.</Description>
-<Xref>PDB:3RFA</Xref>
-<Note>X-ray diffraction, 2.05 angstroms; trapped S-methyl-cysteine intermediate</Note>
-</ReferenceBlock>
-<Comment>For methylated--DNA--[protein]-cysteine S-methyltransferase (EC 2.2.1.63), the Enzyme Commission acknowledges that "This enzyme catalyses only one turnover and therefore is not strictly catalytic."</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-<EnzymeName>methylated--DNA--[protein]-cysteine S-methyltransferase (EC 2.2.1.63)</EnzymeName>
-<EnzymeName>protein-cysteine methyltransferase, NleE (EC 2.2.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>GO:0018125</Xref>
-<Xref>GO:0018320</Xref>
-<Xref>PSI-MOD:00239</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>methylated amino acid</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="act_site__s-methylcysteine intermediate__c">ACT_SITE S-methylcysteine intermediate</Feature>
-<Feature type="UniProt" key="mod_res__s-methylcysteine__c">MOD_RES S-methylcysteine</Feature>
-</Features>
-<Image src="/images/AA0234.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0234.PDB" />
-</Entry>
-<Entry id="AA0235">
-<Header>
-<Code>AA0235</Code>
-<Dates>
-<CreationDate>08-Nov-1996</CreationDate>
-<StrucRevDate>08-Nov-1996</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>4-hydroxy-L-lysine</Name>
-<AlternateName>alpha,epsilon-diamino-gamma-hydroxycaproic acid</AlternateName>
-<AlternateName>L-threo-gamma-hydroxylysine</AlternateName>
-<SystematicName>(2S,4R)-2,6-diamino-4-hydroxyhexanoic acid</SystematicName>
-<Xref>CAS:60594-62-9</Xref>
-<Xref>ChEBI:86271</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 12 N 2 O 2</Formula>
-<Weight type="chemical">144.17</Weight>
-<Weight type="physical">144.089878</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 0 H 0 N 0 O 1</Formula>
-<Weight type="chemical">16.00</Weight>
-<Weight type="physical">15.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sidler, W.</Author>
-<Author>Kumpf, B.</Author>
-<Author>Suter, F.</Author>
-<Author>Morisset, W.</Author>
-<Author>Wehrmeyer, W.</Author>
-<Author>Zuber, H.</Author>
-</Authors>
-<Citation>Biol. Chem. Hoppe-Seyler 366, 233-244, 1985</Citation>
-<Title>Structural studies on cryptomonad biliprotein subunits. Two different alpha-subunits in Chroomonas phycocyanin-645 and Cryptomonas phycoerythrin-545.</Title>
-<Xref>PMID:4005040</Xref>
-<Note>chromatographic evidence with no comparison to 5-hydroxylysine; the stereochemistry was not established</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Feng, T.</Author>
-<Author>Yamamoto, A.</Author>
-<Author>Wilkins, S.E.</Author>
-<Author>Sokolova, E.</Author>
-<Author>Yates, L.A.</Author>
-<Author>Münzel, M.</Author>
-<Author>Singh, P.</Author>
-<Author>Hopkinson, R.J.</Author>
-<Author>Fischer, R.</Author>
-<Author>Cockman, M.E.</Author>
-<Author>Shelley, J.</Author>
-<Author>Trudgian, D.C.</Author>
-<Author>Schödel, J.</Author>
-<Author>McCullagh, J.S.</Author>
-<Author>Ge, W.</Author>
-<Author>Kessler, B.M.</Author>
-<Author>Gilbert, R.J.</Author>
-<Author>Frolova, L.Y.</Author>
-<Author>Alkalaeva, E.</Author>
-<Author>Ratcliffe, P.J.</Author>
-<Author>Schofield, C.J.</Author>
-<Author>Coleman, M.L.</Author>
-</Authors>
-<Citation>Mol. Cell 53, 645-654, 2014</Citation>
-<Title>Optimal translational termination requires C4 lysyl hydroxylation of eRF1.</Title>
-<Xref>DOI:10.1016/j.molcel.2013.12.028</Xref>
-<Xref>PMID:24486019</Xref>
-<Note>chromatographic and mass spectrometric identification</Note>
-</ReferenceBlock>
-<Comment>5-Hydroxy-L-lysine (see RESID:AA0028) was found at a homologous position in the closely related species Rhodomonas CS24. See also RESID:AA0370.</Comment>
-<Comment>The (2S,4R) diastereomer is shown.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>[protein]-lysine 4-dioxygenase, Jmjd4 (EC 1.14.11.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>GO:0018396</Xref>
-<Xref>PSI-MOD:00240</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not currently annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0235.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0235.PDB" />
-</Entry>
-<Entry id="AA0236">
-<Header>
-<Code>AA0236</Code>
-<Dates>
-<CreationDate>08-Nov-1996</CreationDate>
-<StrucRevDate>22-Nov-1996</StrucRevDate>
-<TextChngDate>30-Sep-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N4-hydroxymethyl-L-asparagine</Name>
-<AlternateName>2-amino-N4-hydroxymethylbutanediamic acid</AlternateName>
-<AlternateName>beta-hydroxymethylasparagine</AlternateName>
-<AlternateName>N(gamma)-hydroxymethylasparagine</AlternateName>
-<AlternateName>N4-hydroxymethylasparagine</AlternateName>
-<SystematicName>(2S)-2-amino-4-[(hydroxymethyl)amino]-4-oxobutanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 8 N 2 O 3</Formula>
-<Weight type="chemical">144.13</Weight>
-<Weight type="physical">144.053492</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0003">
-<Formula>C 1 H 2 N 0 O 1</Formula>
-<Weight type="chemical">30.03</Weight>
-<Weight type="physical">30.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Minami, Y.</Author>
-<Author>Yamada, F.</Author>
-<Author>Hase, T.</Author>
-<Author>Matsubara, H.</Author>
-<Author>Murakami, A.</Author>
-<Author>Fujita, Y.</Author>
-<Author>Takao, T.</Author>
-<Author>Shimonishi, Y.</Author>
-</Authors>
-<Citation>FEBS Lett. 191, 216-220, 1985</Citation>
-<Title>Amino acid sequences of allophycocyanin alpha- and beta-subunits isolated from Anabaena cylindrica.</Title>
-<Xref>DOI:10.1016/0014-5793(85)80011-9</Xref>
-<Note>chromatographic and mass spectrometric characterization</Note>
-</ReferenceBlock>
-<Comment>N4-methyl-L-asparagine (see RESID:AA0070) was found at a homologous position in the closely related species Anabaena variabilis. Since the peptide containing this modification was obtained by enzymatic cleavage, not cyanogen bromide cleavage, it could have experienced oxidation of the following methionine residue, leading to the erroneous attribution of a mass of 29 for the modification rather than 14.</Comment>
-<SequenceCode>
-<SequenceSpec>N</SequenceSpec>
-<Xref>GO:0018311</Xref>
-<Xref>PSI-MOD:00241</Xref>
-</SequenceCode>
-<Source>deprecated</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-<Keyword>methylated amino acid</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this dubious modification is not currently annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0236.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0236.PDB" />
-</Entry>
-<Entry id="AA0237">
-<Header>
-<Code>AA0237</Code>
-<Dates>
-<CreationDate>22-Nov-1996</CreationDate>
-<StrucRevDate>22-Nov-1996</StrucRevDate>
-<TextChngDate>30-Sep-2008</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-(ADP-ribosyl)-L-serine</Name>
-<AlternateName>O3-(ADP-ribosyl)-L-serine</AlternateName>
-<AlternateName>O3-alpha-D-ribofuranosyl-L-serine 5'-&gt;5'-ester with adenosine 5'-(trihydrogen diphosphate)</AlternateName>
-<AlternateName>O3-[alpha-D-ribofuranoside 5'-&gt;5'-ester with adenosine 5'-(trihydrogen diphosphate)]-L-serine</AlternateName>
-<SystematicName>(S)-2-amino-3-([adenosine 5'-(trihydrogen diphosphate) 5'-&gt;5'-ester with alpha-D-ribofuranosyl]oxy)-propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 18 H 26 N 6 O 15 P 2</Formula>
-<Weight type="chemical">628.38</Weight>
-<Weight type="physical">628.093137</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 15 H 21 N 5 O 13 P 2</Formula>
-<Weight type="chemical">541.30</Weight>
-<Weight type="physical">541.061109</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bokoch, G.M.</Author>
-<Author>Parkos, C.A.</Author>
-<Author>Mumby, S.M.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 263, 16744-16749, 1988</Citation>
-<Title>Purification and characterization of the 22,000-Dalton GTP-binding protein substrate for ADP-ribosylation by botulinum toxin, G-22K.</Title>
-<Xref>PMID:3141412</Xref>
-<Note>ADP-ribosylation detected; neither the residue nor the location is determined</Note>
-</ReferenceBlock>
-<Comment>It is not known whether botulinum exoenzyme C3 catalyzes formation of the alpha or beta isomer. The alpha form is presented.</Comment>
-<Comment>The keyword "phosphoprotein" is not used with toxin modification.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>NAD(P)+--serine ADP-ribosyltransferase (EC 2.4.2.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>GO:0006471</Xref>
-<Xref>GO:0018312</Xref>
-<Xref>PSI-MOD:00242</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>*phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__adp-ribosylserine__s">MOD_RES ADP-ribosylserine</Feature>
-</Features>
-<Image src="/images/AA0237.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0237.PDB" />
-</Entry>
-<Entry id="AA0238">
-<Header>
-<Code>AA0238</Code>
-<Dates>
-<CreationDate>06-Dec-1996</CreationDate>
-<StrucRevDate>06-Dec-1996</StrucRevDate>
-<TextChngDate>25-Feb-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-cysteine oxazole-4-carboxylic acid</Name>
-<AlternateName>2-(1-azanyl-2-sulfanylethyl)-4-oxazolecarboxylic acid</AlternateName>
-<SystematicName>2-[(1R)-1-amino-2-sulfanylethyl]-1,3-oxazole-4-carboxylic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 6 N 2 O 2 S 1</Formula>
-<Weight type="chemical">170.19</Weight>
-<Weight type="physical">170.014998</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0016">
-<Formula>C 0 H -4 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-20.03</Weight>
-<Weight type="physical">-20.026215</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Li, Y.M.</Author>
-<Author>Milne, J.C.</Author>
-<Author>Madison, L.L.</Author>
-<Author>Kolter, R.</Author>
-<Author>Walsh, C.T.</Author>
-</Authors>
-<Citation>Science 274, 1188-1193, 1996</Citation>
-<Title>From peptide precursors to oxazole and thiazole-containing peptide antibiotics: microcin B17 synthase.</Title>
-<Xref>DOI:10.1126/science.274.5290.1188</Xref>
-<Xref>PMID:8895467</Xref>
-<Note>mass spectrometric identification of peptides and biosynthetic intermediates</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yorgey, P.</Author>
-<Author>Lee, J.</Author>
-<Author>Koerdel, J.</Author>
-<Author>Vivas, E.</Author>
-<Author>Warner, P.</Author>
-<Author>Jebaratnam, D.</Author>
-<Author>Kolter, R.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 91, 4519-4523, 1994</Citation>
-<Title>Posttranslational modifications in microcin B17 define an additional class of DNA gyrase inhibitor.</Title>
-<Xref>DOI:10.1073/pnas.91.10.4519</Xref>
-<Xref>PMID:8183941</Xref>
-<Note>(1)H-NMR identification</Note>
-</ReferenceBlock>
-<Comment>Formed by the condensation of a serine hydroxyl with the carbonyl of the preceding residue and alpha-beta dehydrogenation.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptidyl-serine cyclase (EC 4.2.1.-)</EnzymeName>
-<EnzymeName>peptidyl-oxazoline dehydrogenase (EC 1.3.-.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C, S</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Xref>GO:0018132</Xref>
-<Xref>PSI-MOD:00243</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>oxazole/thiazole ring</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__oxazole-4-carboxylic acid (cys-ser)__c__s">CROSSLNK Oxazole-4-carboxylic acid (Cys-Ser)</Feature>
-</Features>
-<Image src="/images/AA0238.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0238.PDB" />
-</Entry>
-<Entry id="AA0239">
-<Header>
-<Code>AA0239</Code>
-<Dates>
-<CreationDate>06-Dec-1996</CreationDate>
-<StrucRevDate>06-Dec-1996</StrucRevDate>
-<TextChngDate>25-Feb-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-cysteine oxazoline-4-carboxylic acid</Name>
-<AlternateName>2-[1-azanyl-2-sulfanylethyl]-4,5-dihydro-1,3-oxazole-4-carboxylic acid</AlternateName>
-<SystematicName>(4S)-2-[(1R)-1-amino-2-sulfanylethyl]-4,5-dihydro-1,3-oxazole-4-carboxylic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 8 N 2 O 2 S 1</Formula>
-<Weight type="chemical">172.20</Weight>
-<Weight type="physical">172.030649</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0016">
-<Formula>C 0 H -2 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kettenring, J.</Author>
-<Author>Colombo, L.</Author>
-<Author>Ferrari, P.</Author>
-<Author>Tavecchia, P.</Author>
-<Author>Nebuloni, M.</Author>
-<Author>Vekey, K.</Author>
-<Author>Gallo, G.G.</Author>
-<Author>Selva, E.</Author>
-</Authors>
-<Citation>J. Antibiot. 44, 702-715, 1991</Citation>
-<Title>Antibiotic GE2270 A: a novel inhibitor of bacterial protein synthesis. II. Structure elucidation.</Title>
-<Xref>PMID:1880060</Xref>
-<Note>mass spectrometric, (1)H-NMR, (13)C-NMR, and IR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Tavecchia, P.</Author>
-<Author>Gentili, P.</Author>
-<Author>Kurz, M.</Author>
-<Author>Sottani, C.</Author>
-<Author>Bonfichi, R.</Author>
-<Author>Lociuro, S.</Author>
-<Author>Selva, E.</Author>
-</Authors>
-<Citation>J. Antibiot. 47, 1564-1567, 1994</Citation>
-<Title>Revised structure of the antibiotic GE 2270A.</Title>
-<Xref>PMID:7844053</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Heffron, S.E.</Author>
-<Author>Jurnak, F.</Author>
-</Authors>
-<Citation>Biochemistry 39, 37-45, 2000</Citation>
-<Title>Structure of an EF-Tu complex with a thiazolyl peptide antibiotic determined at 2.35 A resolution: atomic basis for GE2270A inhibition of EF-Tu.</Title>
-<Xref>DOI:10.1021/bi9913597</Xref>
-<Xref>PMID:10625477</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Heffron, S.E.</Author>
-<Author>Jurnak, F.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, October 1999</Citation>
-<Description>Crystal structure of elongation factor, Tu (EF-Tu-MGGDP) complexed with GE2270A, a thiazolyl peptide antibiotic.</Description>
-<Xref>PDB:1D8T</Xref>
-<Note>X-ray diffraction, 2.35 angstroms</Note>
-</ReferenceBlock>
-<Comment>Formed by the condensation of a serine hydroxyl with the carbonyl of the preceding residue.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptidyl-serine cyclase (EC 4.2.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C, S</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Xref>GO:0018133</Xref>
-<Xref>PSI-MOD:00244</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>oxazole/thiazole ring</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__oxazoline-4-carboxylic acid (cys-ser)__c__s">CROSSLNK Oxazoline-4-carboxylic acid (Cys-Ser)</Feature>
-</Features>
-<Image src="/images/AA0239.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0239.PDB" />
-</Entry>
-<Entry id="AA0240">
-<Header>
-<Code>AA0240</Code>
-<Dates>
-<CreationDate>06-Dec-1996</CreationDate>
-<StrucRevDate>06-Dec-1996</StrucRevDate>
-<TextChngDate>25-Feb-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>glycine oxazole-4-carboxylic acid</Name>
-<AlternateName>2-azanylmethyl-1,3-oxazole-4-carboxylic acid</AlternateName>
-<SystematicName>2-aminomethyl-1,3-oxazole-4-carboxylic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 4 N 2 O 2</Formula>
-<Weight type="chemical">124.10</Weight>
-<Weight type="physical">124.027277</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0008 AA0016">
-<Formula>C 0 H -4 N 0 O -1</Formula>
-<Weight type="chemical">-20.03</Weight>
-<Weight type="physical">-20.026215</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Li, Y.M.</Author>
-<Author>Milne, J.C.</Author>
-<Author>Madison, L.L.</Author>
-<Author>Kolter, R.</Author>
-<Author>Walsh, C.T.</Author>
-</Authors>
-<Citation>Science 274, 1188-1193, 1996</Citation>
-<Title>From peptide precursors to oxazole and thiazole-containing peptide antibiotics: microcin B17 synthase.</Title>
-<Xref>DOI:10.1126/science.274.5290.1188</Xref>
-<Xref>PMID:8895467</Xref>
-<Note>mass spectrometric identification of peptides and biosynthetic intermediates</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yorgey, P.</Author>
-<Author>Lee, J.</Author>
-<Author>Koerdel, J.</Author>
-<Author>Vivas, E.</Author>
-<Author>Warner, P.</Author>
-<Author>Jebaratnam, D.</Author>
-<Author>Kolter, R.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 91, 4519-4523, 1994</Citation>
-<Title>Posttranslational modifications in microcin B17 define an additional class of DNA gyrase inhibitor.</Title>
-<Xref>DOI:10.1073/pnas.91.10.4519</Xref>
-<Xref>PMID:8183941</Xref>
-<Note>(1)H-NMR identification</Note>
-</ReferenceBlock>
-<Comment>Formed by the condensation of a serine hydroxyl with the carbonyl of the preceding residue and alpha-beta dehydrogenation.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptidyl-serine cyclase (EC 4.2.1.-)</EnzymeName>
-<EnzymeName>peptidyl-oxazoline dehydrogenase (EC 1.3.-.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>G, S</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Xref>GO:0018134</Xref>
-<Xref>PSI-MOD:00245</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>oxazole/thiazole ring</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__oxazole-4-carboxylic acid (gly-ser)__g__s">CROSSLNK Oxazole-4-carboxylic acid (Gly-Ser)</Feature>
-</Features>
-<Image src="/images/AA0240.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0240.PDB" />
-</Entry>
-<Entry id="AA0241">
-<Header>
-<Code>AA0241</Code>
-<Dates>
-<CreationDate>06-Dec-1996</CreationDate>
-<StrucRevDate>06-Dec-1996</StrucRevDate>
-<TextChngDate>30-Sep-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>glycine thiazole-4-carboxylic acid</Name>
-<AlternateName>2-(azanylmethyl)-1,3-thiazole-4-carboxylic acid</AlternateName>
-<SystematicName>2-(aminomethyl)-1,3-thiazole-4-carboxylic acid</SystematicName>
-<Xref>CAS:25438-22-6</Xref>
-<Xref>ChEBI:21276</Xref>
-<Xref>PDBHET:BB9</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 4 N 2 O 1 S 1</Formula>
-<Weight type="chemical">140.16</Weight>
-<Weight type="physical">140.004434</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0008 AA0005">
-<Formula>C 0 H -4 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-20.03</Weight>
-<Weight type="physical">-20.026215</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Li, Y.M.</Author>
-<Author>Milne, J.C.</Author>
-<Author>Madison, L.L.</Author>
-<Author>Kolter, R.</Author>
-<Author>Walsh, C.T.</Author>
-</Authors>
-<Citation>Science 274, 1188-1193, 1996</Citation>
-<Title>From peptide precursors to oxazole and thiazole-containing peptide antibiotics: microcin B17 synthase.</Title>
-<Xref>DOI:10.1126/science.274.5290.1188</Xref>
-<Xref>PMID:8895467</Xref>
-<Note>mass spectrometric identification of peptides and biosynthetic intermediates</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yorgey, P.</Author>
-<Author>Lee, J.</Author>
-<Author>Koerdel, J.</Author>
-<Author>Vivas, E.</Author>
-<Author>Warner, P.</Author>
-<Author>Jebaratnam, D.</Author>
-<Author>Kolter, R.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 91, 4519-4523, 1994</Citation>
-<Title>Posttranslational modifications in microcin B17 define an additional class of DNA gyrase inhibitor.</Title>
-<Xref>DOI:10.1073/pnas.91.10.4519</Xref>
-<Xref>PMID:8183941</Xref>
-<Note>(1)H-NMR identification</Note>
-</ReferenceBlock>
-<Comment>Formed by the condensation of a cysteine thiol with the carbonyl of the preceding residue and alpha-beta dehydrogenation.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptidyl-cysteine cyclase (EC 4.2.1.-)</EnzymeName>
-<EnzymeName>peptidyl-thiazoline dehydrogenase (EC 1.3.-.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C, G</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Xref>GO:0018137</Xref>
-<Xref>PSI-MOD:00246</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>oxazole/thiazole ring</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__thiazole-4-carboxylic acid (gly-cys)__g__c">CROSSLNK Thiazole-4-carboxylic acid (Gly-Cys)</Feature>
-</Features>
-<Image src="/images/AA0241.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0241.PDB" />
-</Entry>
-<Entry id="AA0242">
-<Header>
-<Code>AA0242</Code>
-<Dates>
-<CreationDate>06-Dec-1996</CreationDate>
-<StrucRevDate>06-Dec-1996</StrucRevDate>
-<TextChngDate>30-Sep-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-serine thiazole-4-carboxylic acid</Name>
-<AlternateName>2-[1-azanyl-2-hydroxyethyl]-1,3-thiazole-4-carboxylic acid</AlternateName>
-<SystematicName>2-[(1S)-1-amino-2-hydroxyethyl]-1,3-thiazole-4-carboxylic acid</SystematicName>
-<Xref>PDBHET:BB9</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 6 N 2 O 2 S 1</Formula>
-<Weight type="chemical">170.19</Weight>
-<Weight type="physical">170.014998</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016 AA0005">
-<Formula>C 0 H -4 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-20.03</Weight>
-<Weight type="physical">-20.026215</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Li, Y.M.</Author>
-<Author>Milne, J.C.</Author>
-<Author>Madison, L.L.</Author>
-<Author>Kolter, R.</Author>
-<Author>Walsh, C.T.</Author>
-</Authors>
-<Citation>Science 274, 1188-1193, 1996</Citation>
-<Title>From peptide precursors to oxazole and thiazole-containing peptide antibiotics: microcin B17 synthase.</Title>
-<Xref>DOI:10.1126/science.274.5290.1188</Xref>
-<Xref>PMID:8895467</Xref>
-<Note>mass spectrometric identification of peptides and biosynthetic intermediates</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yorgey, P.</Author>
-<Author>Lee, J.</Author>
-<Author>Koerdel, J.</Author>
-<Author>Vivas, E.</Author>
-<Author>Warner, P.</Author>
-<Author>Jebaratnam, D.</Author>
-<Author>Kolter, R.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 91, 4519-4523, 1994</Citation>
-<Title>Posttranslational modifications in microcin B17 define an additional class of DNA gyrase inhibitor.</Title>
-<Xref>DOI:10.1073/pnas.91.10.4519</Xref>
-<Xref>PMID:8183941</Xref>
-<Note>(1)H-NMR identification</Note>
-</ReferenceBlock>
-<Comment>Formed by the condensation of a cysteine thiol with the carbonyl of the preceding residue and alpha-beta dehydrogenation.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptidyl-cysteine cyclase (EC 4.2.1.-)</EnzymeName>
-<EnzymeName>peptidyl-thiazoline dehydrogenase (EC 1.3.-.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C, S</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Xref>GO:0018138</Xref>
-<Xref>PSI-MOD:00247</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>oxazole/thiazole ring</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__thiazole-4-carboxylic acid (ser-cys)__s__c">CROSSLNK Thiazole-4-carboxylic acid (Ser-Cys)</Feature>
-</Features>
-<Image src="/images/AA0242.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0242.PDB" />
-</Entry>
-<Entry id="AA0243">
-<Header>
-<Code>AA0243</Code>
-<Dates>
-<CreationDate>06-Dec-1996</CreationDate>
-<StrucRevDate>06-Dec-1996</StrucRevDate>
-<TextChngDate>30-Sep-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-phenylalanine thiazole-4-carboxylic acid</Name>
-<AlternateName>2-[1-azanyl-2-phenylethyl]-1,3-thiazole-4-carboxylic acid</AlternateName>
-<SystematicName>2-[(1S)-1-amino-2-phenylethyl]-1,3-thiazole-4-carboxylic acid</SystematicName>
-<Xref>PDBHET:BB9</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 12 H 10 N 2 O 1 S 1</Formula>
-<Weight type="chemical">230.29</Weight>
-<Weight type="physical">230.051384</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0014 AA0005">
-<Formula>C 0 H -4 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-20.03</Weight>
-<Weight type="physical">-20.026215</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kettenring, J.</Author>
-<Author>Colombo, L.</Author>
-<Author>Ferrari, P.</Author>
-<Author>Tavecchia, P.</Author>
-<Author>Nebuloni, M.</Author>
-<Author>Vekey, K.</Author>
-<Author>Gallo, G.G.</Author>
-<Author>Selva, E.</Author>
-</Authors>
-<Citation>J. Antibiot. 44, 702-715, 1991</Citation>
-<Title>Antibiotic GE2270 A: a novel inhibitor of bacterial protein synthesis. II. Structure elucidation.</Title>
-<Xref>PMID:1880060</Xref>
-<Note>mass spectrometric, (1)H-NMR, (13)C-NMR, and IR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Tavecchia, P.</Author>
-<Author>Gentili, P.</Author>
-<Author>Kurz, M.</Author>
-<Author>Sottani, C.</Author>
-<Author>Bonfichi, R.</Author>
-<Author>Lociuro, S.</Author>
-<Author>Selva, E.</Author>
-</Authors>
-<Citation>J. Antibiot. 47, 1564-1567, 1994</Citation>
-<Title>Revised structure of the antibiotic GE 2270A.</Title>
-<Xref>PMID:7844053</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Heffron, S.E.</Author>
-<Author>Jurnak, F.</Author>
-</Authors>
-<Citation>Biochemistry 39, 37-45, 2000</Citation>
-<Title>Structure of an EF-Tu complex with a thiazolyl peptide antibiotic determined at 2.35 A resolution: atomic basis for GE2270A inhibition of EF-Tu.</Title>
-<Xref>DOI:10.1021/bi9913597</Xref>
-<Xref>PMID:10625477</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Heffron, S.E.</Author>
-<Author>Jurnak, F.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, October 1999</Citation>
-<Description>Crystal structure of elongation factor, Tu (EF-Tu-MGGDP) complexed with GE2270A, a thiazolyl peptide antibiotic.</Description>
-<Xref>PDB:1D8T</Xref>
-<Note>X-ray diffraction, 2.35 angstroms</Note>
-</ReferenceBlock>
-<Comment>Formed by the condensation of a cysteine thiol with the carbonyl of the preceding residue and alpha-beta dehydrogenation.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptidyl-cysteine cyclase (EC 4.2.1.-)</EnzymeName>
-<EnzymeName>peptidyl-thiazoline dehydrogenase (EC 1.3.-.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C, F</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Xref>GO:0018139</Xref>
-<Xref>PSI-MOD:00248</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>oxazole/thiazole ring</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__thiazole-4-carboxylic acid (phe-cys)__f__c">CROSSLNK Thiazole-4-carboxylic acid (Phe-Cys)</Feature>
-</Features>
-<Image src="/images/AA0243.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0243.PDB" />
-</Entry>
-<Entry id="AA0244">
-<Header>
-<Code>AA0244</Code>
-<Dates>
-<CreationDate>06-Dec-1996</CreationDate>
-<StrucRevDate>06-Dec-1996</StrucRevDate>
-<TextChngDate>30-Sep-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-cysteine thiazole-4-carboxylic acid</Name>
-<AlternateName>2-[1-azanyl-2-sulfanylethyl]-1,3-thiazole-4-carboxylic acid</AlternateName>
-<SystematicName>2-[(1S)-1-amino-2-sulfanylethyl]-1,3-thiazole-4-carboxylic acid</SystematicName>
-<Xref>PDBHET:BB9</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 6 N 2 O 1 S 2</Formula>
-<Weight type="chemical">186.25</Weight>
-<Weight type="physical">185.992155</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005">
-<Formula>C 0 H -4 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-20.03</Weight>
-<Weight type="physical">-20.026215</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kettenring, J.</Author>
-<Author>Colombo, L.</Author>
-<Author>Ferrari, P.</Author>
-<Author>Tavecchia, P.</Author>
-<Author>Nebuloni, M.</Author>
-<Author>Vekey, K.</Author>
-<Author>Gallo, G.G.</Author>
-<Author>Selva, E.</Author>
-</Authors>
-<Citation>J. Antibiot. 44, 702-715, 1991</Citation>
-<Title>Antibiotic GE2270 A: a novel inhibitor of bacterial protein synthesis. II. Structure elucidation.</Title>
-<Xref>PMID:1880060</Xref>
-<Note>mass spectrometric, (1)H-NMR, (13)C-NMR, and IR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Tavecchia, P.</Author>
-<Author>Gentili, P.</Author>
-<Author>Kurz, M.</Author>
-<Author>Sottani, C.</Author>
-<Author>Bonfichi, R.</Author>
-<Author>Lociuro, S.</Author>
-<Author>Selva, E.</Author>
-</Authors>
-<Citation>J. Antibiot. 47, 1564-1567, 1994</Citation>
-<Title>Revised structure of the antibiotic GE 2270A.</Title>
-<Xref>PMID:7844053</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Heffron, S.E.</Author>
-<Author>Jurnak, F.</Author>
-</Authors>
-<Citation>Biochemistry 39, 37-45, 2000</Citation>
-<Title>Structure of an EF-Tu complex with a thiazolyl peptide antibiotic determined at 2.35 A resolution: atomic basis for GE2270A inhibition of EF-Tu.</Title>
-<Xref>DOI:10.1021/bi9913597</Xref>
-<Xref>PMID:10625477</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Heffron, S.E.</Author>
-<Author>Jurnak, F.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, October 1999</Citation>
-<Description>Crystal structure of elongation factor, Tu (EF-Tu-MGGDP) complexed with GE2270A, a thiazolyl peptide antibiotic.</Description>
-<Xref>PDB:1D8T</Xref>
-<Note>X-ray diffraction, 2.35 angstroms</Note>
-</ReferenceBlock>
-<Comment>Formed by the condensation of a cysteine thiol with the carbonyl of the preceding residue and alpha-beta dehydrogenation.</Comment>
-<Comment>The first cysteine may be condensed on the carbonyl of the residue preceding it, forming a 2,4'-bithiazole structure.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptidyl-cysteine cyclase (EC 4.2.1.-)</EnzymeName>
-<EnzymeName>peptidyl-thiazoline dehydrogenase (EC 1.3.-.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C, C</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Xref>GO:0018140</Xref>
-<Xref>PSI-MOD:00249</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>oxazole/thiazole ring</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__thiazole-4-carboxylic acid (cys-cys)__c__c">CROSSLNK Thiazole-4-carboxylic acid (Cys-Cys)</Feature>
-</Features>
-<Image src="/images/AA0244.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0244.PDB" />
-</Entry>
-<Entry id="AA0245">
-<Header>
-<Code>AA0245</Code>
-<Dates>
-<CreationDate>06-Dec-1996</CreationDate>
-<StrucRevDate>06-Dec-1996</StrucRevDate>
-<TextChngDate>25-Feb-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-lysine thiazole-4-carboxylic acid</Name>
-<AlternateName>2-[1,5-bis(azanyl)pentyl]-1,3-thiazole-4-carboxylic acid</AlternateName>
-<SystematicName>2-[(1S)-1,5-diaminopentyl]-1,3-thiazole-4-carboxylic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 13 N 3 O 1 S 1</Formula>
-<Weight type="chemical">211.28</Weight>
-<Weight type="physical">211.077933</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012 AA0005">
-<Formula>C 0 H -4 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-20.03</Weight>
-<Weight type="physical">-20.026215</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kettenring, J.</Author>
-<Author>Colombo, L.</Author>
-<Author>Ferrari, P.</Author>
-<Author>Tavecchia, P.</Author>
-<Author>Nebuloni, M.</Author>
-<Author>Vekey, K.</Author>
-<Author>Gallo, G.G.</Author>
-<Author>Selva, E.</Author>
-</Authors>
-<Citation>J. Antibiot. 44, 702-715, 1991</Citation>
-<Title>Antibiotic GE2270 A: a novel inhibitor of bacterial protein synthesis. II. Structure elucidation.</Title>
-<Xref>PMID:1880060</Xref>
-<Note>mass spectrometric, (1)H-NMR, (13)C-NMR, and IR identification</Note>
-</ReferenceBlock>
-<Comment>Lysine is now thought not to be encoded in the peptide sequence modified to produce GE2270. See RESID:AA0470.</Comment>
-<SequenceCode>
-<SequenceSpec>C, K</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Xref>GO:0018141</Xref>
-<Xref>PSI-MOD:00250</Xref>
-</SequenceCode>
-<Source>deprecated</Source>
-<Keywords>
-<Keyword>oxazole/thiazole ring</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this dubious modification is not currently annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0245.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0245.PDB" />
-</Entry>
-<Entry id="AA0246">
-<Header>
-<Code>AA0246</Code>
-<Dates>
-<CreationDate>28-Feb-1997</CreationDate>
-<StrucRevDate>28-Feb-1997</StrucRevDate>
-<TextChngDate>30-Apr-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-(phospho-5'-DNA)-L-serine</Name>
-<AlternateName>O3-(phospho-5'-DNA)-L-serine</AlternateName>
-<AlternateName>O3-L-serine 5'-DNA phosphodiester</AlternateName>
-<SystematicName>(S)-2-amino-3-(5'-deoxyribonucleic acid phosphonoxy)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 5 N 1 O 5 P 1 +</Formula>
-<Weight type="chemical">166.05 +</Weight>
-<Weight type="physical">165.990534 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 0 H 0 N 0 O 3 P 1 +</Formula>
-<Weight type="chemical">78.97 +</Weight>
-<Weight type="physical">78.958505 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Desiderio, S.V.</Author>
-<Author>Kelly Jr., T.J.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 145, 319-337, 1981</Citation>
-<Title>Structure of the linkage between adenovirus DNA and the 55,000 molecular weight terminal protein.</Title>
-<Xref>DOI:10.1016/0022-2836(81)90208-4</Xref>
-<Xref>PMID:7265205</Xref>
-<Note>chromatographic detection; chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Smart, J.E.</Author>
-<Author>Stillman, B.W.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 257, 13499-13506, 1982</Citation>
-<Title>Adenovirus terminal protein precursor. Partial amino acid sequence and the site of covalent linkage to virus DNA.</Title>
-<Xref>PMID:7142163</Xref>
-<Note>chromatographic detection; chemical characterization</Note>
-</ReferenceBlock>
-<Comment>The keyword "phosphoprotein" is not used with polynucleotide-linked intermediate modifications.</Comment>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>GO:0018145</Xref>
-<Xref>PSI-MOD:00251</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>*phosphoprotein</Keyword>
-<Keyword>genome-linked protein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="act_site__o-(5&apos;-phospho-dna)-serine intermediate__s">ACT_SITE O-(5'-phospho-DNA)-serine intermediate</Feature>
-<Feature type="UniProt" key="mod_res__o-(5&apos;-phospho-dna)-serine__s">MOD_RES O-(5'-phospho-DNA)-serine</Feature>
-</Features>
-<Image src="/images/AA0246.GIF" alt="DUMMY.GIF" />
-</Entry>
-<Entry id="AA0247">
-<Header>
-<Code>AA0247</Code>
-<Dates>
-<CreationDate>21-Mar-1997</CreationDate>
-<StrucRevDate>21-Mar-1997</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>keratan sulfate D-glucuronosyl-D-galactosyl-D-galactosyl-D-xylosyl-L-threonine</Name>
-<AlternateName>keratosulfate</AlternateName>
-<SystematicName>poly[beta-1,4-(2-acetamido-2-deoxy-6-sulfate D-glucosyl)-beta-1,3-D-galactosyl]-beta-1,4-D-glucopyranuronosyl-beta-1,3-D-galactosyl-beta-1,3-D-galactosyl-beta-1,4-D-xylosyl-beta-1,3-L-threonine</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 6 N 1 O 2 +</Formula>
-<Weight type="chemical">100.10 +</Weight>
-<Weight type="physical">100.039853 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0017">
-<Formula>C 0 H -1 N 0 O 0 +</Formula>
-<Weight type="chemical">-1.01 +</Weight>
-<Weight type="physical">-1.007825 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bourdon, M.A.</Author>
-<Author>Krusius, T.</Author>
-<Author>Campbell, S.</Author>
-<Author>Schwartz, N.B.</Author>
-<Author>Ruoslahti, E.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 84, 3194-3198, 1987</Citation>
-<Title>Identification and synthesis of a recognition signal for the attachment of glycosaminoglycans to proteins.</Title>
-<Xref>DOI:10.1073/pnas.84.10.3194</Xref>
-<Xref>PMID:3472204</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Barry, F.P.</Author>
-<Author>Gaw, J.U.</Author>
-<Author>Young, C.N.</Author>
-<Author>Neame, P.J.</Author>
-</Authors>
-<Citation>Biochem. J. 286, 761-769, 1992</Citation>
-<Title>Hyaluronan-binding region of aggrecan from pig laryngeal cartilage. Amino acid sequence, analysis of N-linked oligosaccharides and location of the keratan sulphate.</Title>
-<Xref>PMID:1417734</Xref>
-<Note>antibody detection during sequencing</Note>
-</ReferenceBlock>
-<Comment>The attachment polysaccharide has not been characterized for all forms of the chondroitin sulfate proteoglycans.</Comment>
-<Comment>See also RESID:AA0155, RESID:AA0399, RESID:AA0401, RESID:AA0403, RESID:AA0405, and RESID:AA0515 for other O-glycosylated threonines.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>protein xylosyltransferase (EC 2.4.2.26)</EnzymeName>
-<EnzymeName>xylosylprotein 4-beta-galactosyltransferase (EC 2.4.1.133)</EnzymeName>
-<EnzymeName>galactosylxylosylprotein 3-beta-galactosyltransferase (EC 2.4.1.134)</EnzymeName>
-<EnzymeName>galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase (EC 2.4.1.135)</EnzymeName>
-<EnzymeName>glucuronylgalactosylproteoglycan beta-1,4-N-acetylgalactosaminyltransferase (EC 2.4.1.174)</EnzymeName>
-<EnzymeName>chondroitin 4-sulfotransferase (EC 2.8.2.5)</EnzymeName>
-<EnzymeName>chondroitin 6-sulfotransferase (EC 2.8.2.17)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>T</SequenceSpec>
-<Xref>GO:0018146</Xref>
-<Xref>GO:0018405</Xref>
-<Xref>PSI-MOD:00252</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chondroitin sulfate proteoglycan</Keyword>
-<Keyword>glycoprotein</Keyword>
-<Keyword>keratan sulfate</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__o-linked (xyl...) (keratan sulfate) threonine__t">CARBOHYD O-linked (Xyl...) (keratan sulfate) threonine</Feature>
-</Features>
-<Image src="/images/AA0247.GIF" alt="DUMMY.GIF" />
-</Entry>
-<Entry id="AA0248">
-<Header>
-<Code>AA0248</Code>
-<Dates>
-<CreationDate>12-Sep-1997</CreationDate>
-<StrucRevDate>07-Sep-2001</StrucRevDate>
-<TextChngDate>31-Mar-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-selenocysteinyl molybdenum bis(molybdopterin guanine dinucleotide)</Name>
-<AlternateName>2-amino-5,6-dimercapto-7-methyl-3,7,8a,9-tetrahydro-8-oxa-1,3,9,10-tetraazaanthracen-4-one guanosine dinucleotide</AlternateName>
-<AlternateName>formate dehydrogenase selenocysteine molybdenum cofactor</AlternateName>
-<SystematicName>bis[8-amino-1a,2,4a,5,6,7,10-heptahydro-2-(trihydrogen diphosphate 5'-ester with guanosine)methyl-6-oxo-3,4-disulfanyl-pteridino[6,7-5,6]pyranoato-S3,S4]-selenocysteinyl-Se-molybdenum</SystematicName>
-<Xref>PDBHET:MGD</Xref>
-<Xref>PDBHET:MO</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 43 H 52 Mo 1 N 21 O 27 P 4 S 4 Se 1</Formula>
-<Weight type="chemical">1722.07</Weight>
-<Weight type="physical">1723.939410</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005" label="CYS">
-<Formula>C 40 H 47 Mo 1 N 20 O 26 P 4 S 3 Se 1</Formula>
-<Weight type="chemical">1618.93</Weight>
-<Weight type="physical">1620.930226</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0022" label="SEC">
-<Formula>C 40 H 47 Mo 1 N 20 O 26 P 4 S 4 Se 0</Formula>
-<Weight type="chemical">1572.02</Weight>
-<Weight type="physical">1572.985775</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Axley, M.J.</Author>
-<Author>Grahame, D.A.</Author>
-<Author>Stadtman, T.C.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 265, 18213-18218, 1990</Citation>
-<Title>Escherichia coli formate-hydrogen lyase. Purification and properties of the selenium-dependent formate dehydrogenase component.</Title>
-<Xref>PMID:2211698</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gladyshev, V.N.</Author>
-<Author>Khangulov, S.V.</Author>
-<Author>Axley, M.J.</Author>
-<Author>Stadtman, T.C.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 91, 7708-7711, 1994</Citation>
-<Title>Coordination of selenium to molybdenum in formate dehydrogenase H from Escherichia coli.</Title>
-<Xref>DOI:10.1073/pnas.91.16.7708</Xref>
-<Xref>PMID:8052647</Xref>
-<Note>selenium coordination of cofactor by EPR</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sun, P.D.</Author>
-<Author>Boyington, J.C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, January 1997</Citation>
-<Description>Reduced form of formate dehydrogenase H from E. coli.</Description>
-<Xref>PDB:1AA6</Xref>
-<Note>X-ray diffraction, 2.3 angstroms, reduced form</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sun, P.D.</Author>
-<Author>Boyington, J.C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, January 1997</Citation>
-<Description>Oxidized form of Formate Dehydrogenase H from E. coli.</Description>
-<Xref>PDB:1FDO</Xref>
-<Note>X-ray diffraction, 2.8 angstroms, oxidized form</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Boyington, J.C.</Author>
-<Author>Gladyshev, V.N.</Author>
-<Author>Khangulov, S.V.</Author>
-<Author>Stadtman, T.C.</Author>
-<Author>Sun, P.D.</Author>
-</Authors>
-<Citation>Science 275, 1305-1308, 1997</Citation>
-<Title>Crystal structure of formate dehydrogenase H: catalysis involving Mo, molybdopterin, selenocysteine, and an Fe4S4 cluster.</Title>
-<Xref>DOI:10.1126/science.275.5304.1305</Xref>
-<Xref>PMID:9036855</Xref>
-<Note>X-ray diffraction</Note>
-</ReferenceBlock>
-<Comment>One possible structure of a reduced form (+4H) is shown. The fully reduced form would be 1a,2,3,4,4a,5,6,7,10-nonahydro. The fully oxidized form would be 2,6,7-trihydro.</Comment>
-<SequenceCode link="CYS">
-<SequenceSpec>C</SequenceSpec>
-<Condition>secondary to RESID:AA0022</Condition>
-<Xref>GO:0018147</Xref>
-<Xref>PSI-MOD:01468</Xref>
-</SequenceCode>
-<SequenceCode link="SEC">
-<SequenceSpec>U</SequenceSpec>
-<Xref>PSI-MOD:00253</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>metalloprotein</Keyword>
-<Keyword>molybdenum</Keyword>
-<Keyword>molybdopterin</Keyword>
-<Keyword>phosphoprotein</Keyword>
-<Keyword>selenium</Keyword>
-<Keyword>selenocysteine</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt" key="metal__molybdenum__c">METAL Molybdenum</Feature>
-<Note>this UniProt feature has a structural misrepresentation</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0248.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0248.PDB" />
-</Entry>
-<Entry id="AA0249">
-<Header>
-<Code>AA0249</Code>
-<Dates>
-<CreationDate>12-Sep-1997</CreationDate>
-<StrucRevDate>12-Sep-1997</StrucRevDate>
-<TextChngDate>20-May-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O4'-(phospho-5'-RNA)-L-tyrosine</Name>
-<AlternateName>O4'-L-tyrosine 5'-RNA phosphodiester</AlternateName>
-<SystematicName>(S)-2-amino-3-[4-(5'-ribonucleic acid phosphonoxy)phenyl]propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 10 N 1 O 5 P 1 +</Formula>
-<Weight type="chemical">243.15 +</Weight>
-<Weight type="physical">243.029659 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0019">
-<Formula>C 0 H 1 N 0 O 3 P 1 +</Formula>
-<Weight type="chemical">79.98 +</Weight>
-<Weight type="physical">79.966331 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ambros, V.</Author>
-<Author>Baltimore, D.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 253, 5263-5266, 1978</Citation>
-<Title>Protein is linked to the 5' end of poliovirus RNA by a phosphodiester linkage to tyrosine.</Title>
-<Xref>PMID:209034</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Rothberg, P.G.</Author>
-<Author>Harris, T.J.</Author>
-<Author>Nomoto, A.</Author>
-<Author>Wimmer, E.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 75, 4868-4872, 1978</Citation>
-<Title>O4-(5'-Uridylyl)tyrosine is the bond between the genome-linked protein and the RNA of poliovirus.</Title>
-<Xref>DOI:10.1038/291547a0</Xref>
-<Xref>PMID:217003</Xref>
-<Note>chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kitamura, N.</Author>
-<Author>Semler, B.L.</Author>
-<Author>Rothberg, P.G.</Author>
-<Author>Larsen, G.R.</Author>
-<Author>Adler, C.J.</Author>
-<Author>Dorner, A.J.</Author>
-<Author>Emini, E.A.</Author>
-<Author>Hanecak, R.</Author>
-<Author>Lee, J.J.</Author>
-<Author>van der Werf, S.</Author>
-<Author>Anderson, C.W.</Author>
-<Author>Wimmer, E.</Author>
-</Authors>
-<Citation>Nature 291, 547-553, 1981</Citation>
-<Title>Primary structure, gene organization and polypeptide expression of poliovirus RNA.</Title>
-<Xref>DOI:10.1038/291547a0</Xref>
-<Xref>PMID:6264310</Xref>
-<Note>protein sequence</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Murphy, J.F.</Author>
-<Author>Rychlik, W.</Author>
-<Author>Rhoads, R.E.</Author>
-<Author>Hunt, A.G.</Author>
-<Author>Shaw, J.G.</Author>
-</Authors>
-<Citation>J. Virol. 65, 511-513, 1991</Citation>
-<Title>A tyrosine residue in the small nuclear inclusion protein of tobacco vein mottling virus links the VPg to the viral RNA.</Title>
-<Xref>PMID:1702164</Xref>
-<Note>chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Olspert, A.</Author>
-<Author>Peil, L.</Author>
-<Author>Hébrard, E.</Author>
-<Author>Fargette, D.</Author>
-<Author>Truve, E.</Author>
-</Authors>
-<Citation>J. Gen. Virol. 92, 445-452, 2011</Citation>
-<Title>Protein-RNA linkage and post-translational modifications of two sobemovirus VPgs.</Title>
-<Xref>DOI:10.1099/vir.0.026476-0</Xref>
-<Xref>PMID:21068217</Xref>
-<Note>mass spectrometric identification; for the genome-linked protein (VPg) of cocksfoot mottle virus, the 5'-end is guanosine and pGp was identified attached to Tyr-5</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>Y</SequenceSpec>
-<Xref>GO:0018148</Xref>
-<Xref>PSI-MOD:00254</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>genome-linked protein</Keyword>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__o-(5&apos;-phospho-rna)-tyrosine__y">MOD_RES O-(5'-phospho-RNA)-tyrosine</Feature>
-</Features>
-<Image src="/images/AA0249.GIF" alt="DUMMY.GIF" />
-</Entry>
-<Entry id="AA0250">
-<Header>
-<Code>AA0250</Code>
-<Dates>
-<CreationDate>21-Nov-1997</CreationDate>
-<StrucRevDate>21-Nov-1997</StrucRevDate>
-<TextChngDate>31-Mar-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>3-(3'-L-histidyl)-L-tyrosine</Name>
-<AlternateName>3-(N3'-histidyl)tyrosine</AlternateName>
-<AlternateName>3-(pi-histidyl)tyrosine</AlternateName>
-<AlternateName>3-(pros-histidyl)tyrosine</AlternateName>
-<AlternateName>beta-(N(delta)-histidyl)tyrosine</AlternateName>
-<AlternateName>beta-(N3'-histidyl)tyrosine</AlternateName>
-<SystematicName>(2S,3R)-2-amino-3-(5-[(2S)-2-amino-2-carboxyethyl]-1H-imidazol-1-yl)-3-(4-hydroxyphenyl)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 15 H 14 N 4 O 3</Formula>
-<Weight type="chemical">298.30</Weight>
-<Weight type="physical">298.106590</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0009 AA0019">
-<Formula>C 0 H -2 N 0 O 0</Formula>
-<Weight type="chemical">-2.02</Weight>
-<Weight type="physical">-2.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bravo, J.</Author>
-<Author>Fita, I.</Author>
-<Author>Ferrer, J.C.</Author>
-<Author>Ens, W.</Author>
-<Author>Hillar, A.</Author>
-<Author>Switala, J.</Author>
-<Author>Loewen, P.C.</Author>
-</Authors>
-<Citation>Protein Sci. 6, 1016-1023, 1997</Citation>
-<Title>Identification of a novel bond between a histidine and the essential tyrosine in catalase HPII of Escherichia coli.</Title>
-<Xref>DOI:10.1002/pro.5560060507</Xref>
-<Xref>PMID:9144772</Xref>
-<Note>X-ray diffraction identification, 1.9 angstroms; mass spectrometric detection</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Melik-Adamyan, W.R.</Author>
-<Author>Bravo, J.</Author>
-<Author>Carpena, X.</Author>
-<Author>Switala, J.</Author>
-<Author>Mate, M.J.</Author>
-<Author>Fita, I.</Author>
-<Author>Loewen, P.C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, August 2000</Citation>
-<Description>Crystal structure of catalase HPII from Escherichia coli, native structure at 1.9 A resolution.</Description>
-<Xref>PDB:1GGE</Xref>
-<Note>X-ray diffraction, 1.89 angstroms</Note>
-</ReferenceBlock>
-<Comment>The chirality of tyrosine C-3 is not specified; from the model it appears to be 3R.</Comment>
-<Comment>This modification is different from the modification 3'-(1'-L-histidyl)-L-tyrosine, see RESID:AA0270.</Comment>
-<SequenceCode>
-<SequenceSpec>H, Y</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>GO:0018150</Xref>
-<Xref>PSI-MOD:00255</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="crosslnk__3&apos;-histidyl-3-tyrosine (his-tyr)__h__y">CROSSLNK 3'-histidyl-3-tyrosine (His-Tyr)</Feature>
-</Features>
-<Image src="/images/AA0250.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0250.PDB" />
-</Entry>
-<Entry id="AA0251">
-<Header>
-<Code>AA0251</Code>
-<Dates>
-<CreationDate>21-Nov-1997</CreationDate>
-<StrucRevDate>21-Nov-1997</StrucRevDate>
-<TextChngDate>31-Mar-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-methionine sulfone</Name>
-<AlternateName>L-methionine S,S-dioxide</AlternateName>
-<AlternateName>S,S-dioxymethionine</AlternateName>
-<SystematicName>(2S)-2-amino-4-(methylsulfonyl)butanoic acid</SystematicName>
-<Xref>CAS:7314-32-1</Xref>
-<Xref>PDBHET:OMT</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 9 N 1 O 3 S 1</Formula>
-<Weight type="chemical">163.19</Weight>
-<Weight type="physical">163.030314</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0013">
-<Formula>C 0 H 0 N 0 O 2 S 0</Formula>
-<Weight type="chemical">32.00</Weight>
-<Weight type="physical">31.989829</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Buzy, A.</Author>
-<Author>Bracchi, V.</Author>
-<Author>Sterjiades, R.</Author>
-<Author>Chroboczek, J.</Author>
-<Author>Thibault, P.</Author>
-<Author>Gagnon, J.</Author>
-<Author>Jouve, H.M.</Author>
-<Author>Hudry-Clergeon, G.</Author>
-</Authors>
-<Citation>J. Protein Chem. 14, 59-72, 1995</Citation>
-<Title>Complete amino acid sequence of Proteus mirabilis PR catalase. Occurrence of a methionine sulfone in the close proximity of the active site.</Title>
-<Xref>DOI:10.1007/BF01888363</Xref>
-<Xref>PMID:7786407</Xref>
-<Note>mass spectrometric detection</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gouet, P.</Author>
-<Author>Jouve, H.M.</Author>
-<Author>Dideberg, O.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 249, 933-954, 1995</Citation>
-<Title>Crystal structure of Proteus mirabilis PR catalase with and without bound NADPH.</Title>
-<Xref>DOI:10.1006/jmbi.1995.0350</Xref>
-<Xref>PMID:7791219</Xref>
-<Note>X-ray diffraction, 2.2 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gouet, P.</Author>
-<Author>Jouve, H.M.</Author>
-<Author>Dideberg, O.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, July 1996</Citation>
-<Description>Structure of Proteus mirabilis PR catalase for the native form (E-Fe(III)) complexed with NADPH.</Description>
-<Xref>PDB:2CAH</Xref>
-<Note>X-ray diffraction, 2.7 angstroms</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>M</SequenceSpec>
-<Xref>GO:0018159</Xref>
-<Xref>PSI-MOD:00256</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="mod_res__methionine sulfone__m">MOD_RES Methionine sulfone</Feature>
-</Features>
-<Image src="/images/AA0251.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0251.PDB" />
-</Entry>
-<Entry id="AA0252">
-<Header>
-<Code>AA0252</Code>
-<Dates>
-<CreationDate>12-Dec-1997</CreationDate>
-<StrucRevDate>18-May-2001</StrucRevDate>
-<TextChngDate>31-Mar-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>dipyrrolylmethanemethyl-L-cysteine</Name>
-<AlternateName>3-[5-(3-acetic acid-4-propanoic acid-1-pyrrol-2-yl)methyl-3-acetic acid-4-propanoic acid-1-pyrrol-2-yl]methylthio-2-aminopropanoic acid</AlternateName>
-<AlternateName>dipyrrole cofactor</AlternateName>
-<AlternateName>dipyrrolylmethyl-L-cysteine</AlternateName>
-<AlternateName>dipyrromethane cofactor</AlternateName>
-<AlternateName>pyrromethane cofactor</AlternateName>
-<SystematicName>(2S)-3-[5-[4-(2-carboxy)ethyl-3-carboxymethyl-1-pyrrol-2-yl]methyl-4-(2-carboxy)ethyl-3-carboxymethyl-1-pyrrol-2-yl]methylthio-2-aminopropanoic acid</SystematicName>
-<Xref>CAS:29261-13-0</Xref>
-<Xref>ChEBI:23842</Xref>
-<Xref>PDBHET:DPM</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 23 H 27 N 3 O 9 S 1</Formula>
-<Weight type="chemical">521.54</Weight>
-<Weight type="physical">521.146800</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 20 H 22 N 2 O 8 S 0</Formula>
-<Weight type="chemical">418.40</Weight>
-<Weight type="physical">418.137616</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Jordan, P.M.</Author>
-<Author>Warren, M.J.</Author>
-<Author>Williams, H.J.</Author>
-<Author>Stolowich, N.J.</Author>
-<Author>Roessner, C.A.</Author>
-<Author>Grant, S.K.</Author>
-<Author>Scott, A.I.</Author>
-</Authors>
-<Citation>FEBS Lett. 235, 189-193, 1988</Citation>
-<Title>Identification of a cysteine residue as the binding site for the dipyrromethane cofactor at the active site of Escherichia coli porphobilinogen deaminase.</Title>
-<Xref>DOI:10.1016/0014-5793(88)81260-2</Xref>
-<Xref>PMID:3042456</Xref>
-<Note>radioisotope labeling; (13)C-NMR characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hart, G.J.</Author>
-<Author>Miller, A.D.</Author>
-<Author>Battersby, A.R.</Author>
-</Authors>
-<Citation>Biochem. J. 252, 909-912, 1988</Citation>
-<Title>Evidence that the pyrromethane cofactor of hydroxymethylbilane synthase (porphobilinogen deaminase) is bound through the sulphur atom of a cysteine residue.</Title>
-<Xref>PMID:3421931</Xref>
-<Note>chemical characterization; (13)C-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Miller, A.D.</Author>
-<Author>Hart, G.J.</Author>
-<Author>Packman, L.C.</Author>
-<Author>Battersby, A.R.</Author>
-</Authors>
-<Citation>Biochem. J. 254, 915-918, 1988</Citation>
-<Title>Evidence that the pyrromethane cofactor of hydroxymethylbilane synthase (porphobilinogen deaminase) is bound to the protein through the sulphur atom of cysteine-242.</Title>
-<Xref>PMID:3196304</Xref>
-<Note>chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Louie, G.V.</Author>
-<Author>Brownlie, P.D.</Author>
-<Author>Lambert, R.</Author>
-<Author>Cooper, J.B.</Author>
-<Author>Blundell, T.L.</Author>
-<Author>Wood, S.P.</Author>
-<Author>Malashkevich, V.N.</Author>
-<Author>Haedener, A.</Author>
-<Author>Warren, M.J.</Author>
-<Author>Shoolingin-Jordan, P.M.</Author>
-</Authors>
-<Citation>Proteins 25, 48-78, 1996</Citation>
-<Title>The three-dimensional structure of Escherichia coli porphobilinogen deaminase at 1.76-angstroms resolution.</Title>
-<Xref>DOI:10.1002/(SICI)1097-0134(199605)25:1&lt;48::AID-PROT5&gt;3.0.CO;2-G</Xref>
-<Xref>PMID:8727319</Xref>
-<Note>X-ray diffraction, 1.76 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Louie, G.V.</Author>
-<Author>Brownlie, P.D.</Author>
-<Author>Lambert, R.</Author>
-<Author>Cooper, J.B.</Author>
-<Author>Blundell, T.L.</Author>
-<Author>Wood, S.P.</Author>
-<Author>Warren, M.J.</Author>
-<Author>Woodcock, S.C.</Author>
-<Author>Jordan, P.M.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, November 1992</Citation>
-<Description>Structure of porphobilinogen deaminase reveals a flexible multidomain polymerase with a single catalytic site.</Description>
-<Xref>PDB:1PDA</Xref>
-<Note>X-ray diffraction, 1.76 angstroms</Note>
-</ReferenceBlock>
-<Comment>The pyrromethane cofactor is synthesized on the enzyme autocatalytically by condensation of two porphobilinogen molecules.</Comment>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>GO:0018160</Xref>
-<Xref>PSI-MOD:00257</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__s-(dipyrrolylmethanemethyl)cysteine__c">MOD_RES S-(dipyrrolylmethanemethyl)cysteine</Feature>
-</Features>
-<Image src="/images/AA0252.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0252.PDB" />
-</Entry>
-<Entry id="AA0253">
-<Header>
-<Code>AA0253</Code>
-<Dates>
-<CreationDate>23-Jan-1998</CreationDate>
-<StrucRevDate>23-Jan-1998</StrucRevDate>
-<TextChngDate>30-Sep-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-(2-aminovinyl)-3-methyl-D-cysteine</Name>
-<AlternateName>2-amino-3-[(2-aminovinyl)sulfanyl]butanoic acid</AlternateName>
-<AlternateName>decarboxylated methyllanthionine</AlternateName>
-<SystematicName>(2S,3S)-2-amino-3-[((Z)-2-aminoethenyl)sulfanyl]butanoic acid</SystematicName>
-<Xref>PDBHET:ABA</Xref>
-<Xref>PDBHET:DBB</Xref>
-<Xref>PDBHET:DHL</Xref>
-<Xref>PDBHET:TEE</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 9 N 2 O 1 S 1</Formula>
-<Weight type="chemical">157.21</Weight>
-<Weight type="physical">157.043559</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0017 AA0005">
-<Formula>C -1 H -4 N 0 O -3 S 0</Formula>
-<Weight type="chemical">-64.04</Weight>
-<Weight type="physical">-64.016044</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Prasch, T.</Author>
-<Author>Naumann, T.</Author>
-<Author>Markert, R.L.M.</Author>
-<Author>Sattler, M.</Author>
-<Author>Schubert, W.</Author>
-<Author>Schaal, S.</Author>
-<Author>Bauch, M.</Author>
-<Author>Kogler, H.</Author>
-<Author>Griesinger, C.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 244, 501-512, 1997</Citation>
-<Title>Constitution and solution conformation of the antibiotic mersacidin determined by NMR and molecular dynamics.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1997.00501.x</Xref>
-<Xref>PMID:9119018</Xref>
-<Note>identification by (1)H- and (13)C-NMR</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Schneider, T.R.</Author>
-<Author>Kärcher, J.</Author>
-<Author>Pohl, E.</Author>
-<Author>Lubini, P.</Author>
-<Author>Sheldrick, G.M.</Author>
-</Authors>
-<Citation>Acta Crystallogr. D Biol. Crystallogr. 56, 705-713, 2000</Citation>
-<Title>Ab initio structure determination of the lantibiotic mersacidin.</Title>
-<Xref>DOI:10.1107/S0907444900003711</Xref>
-<Xref>PMID:10818347</Xref>
-<Note>X-ray diffraction, 1.06 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Schneider, T.R.</Author>
-<Author>Kärcher, J.</Author>
-<Author>Sheldrick, G.M.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, November 1999</Citation>
-<Description>Ab initio structure determination of the lantibiotic mersacidin.</Description>
-<Xref>PDB:1QOW</Xref>
-<Note>X-ray diffraction, 1.06 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Li, B.</Author>
-<Author>Sher, D.</Author>
-<Author>Kelly, L.</Author>
-<Author>Shi, Y.</Author>
-<Author>Huang, K.</Author>
-<Author>Knerr, P.J.</Author>
-<Author>Joewono, I.</Author>
-<Author>Rusch, D.</Author>
-<Author>Chisholm, S.W.</Author>
-<Author>van der Donk, W.A.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 107, 10430-10435, 2010</Citation>
-<Title>Catalytic promiscuity in the biosynthesis of cyclic peptide secondary metabolites in planktonic marine cyanobacteria.</Title>
-<Xref>DOI:10.1073/pnas.0913677107</Xref>
-<Xref>PMID:20479271</Xref>
-</ReferenceBlock>
-<Comment>This cross-link arises from the decarboxylation of the carboxyl-terminal portion of 3-methyllanthionine.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptidyl-phosphoserine/phosphothreonine dehydratase (EC 4.2.1.-)</EnzymeName>
-<EnzymeName>peptidyl-cysteine dehydroalanine/dehydrobutyrine ligase (EC 6.2.-.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C, T</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Condition>cross-link 2</Condition>
-<Xref>GO:0018162</Xref>
-<Xref>PSI-MOD:00258</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>lanthionine</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__s-(2-aminovinyl)-3-methyl-d-cysteine (thr-cys)__t__c">CROSSLNK S-(2-aminovinyl)-3-methyl-D-cysteine (Thr-Cys)</Feature>
-</Features>
-<Image src="/images/AA0253.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0253.PDB" />
-</Entry>
-<Entry id="AA0254">
-<Header>
-<Code>AA0254</Code>
-<Dates>
-<CreationDate>29-May-1998</CreationDate>
-<StrucRevDate>29-May-1998</StrucRevDate>
-<TextChngDate>30-Apr-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O4'-(phospho-5'-DNA)-L-tyrosine</Name>
-<AlternateName>O4'-L-tyrosine 5'-DNA phosphodiester</AlternateName>
-<SystematicName>(S)-2-amino-3-[4-(5'-deoxyribonucleic acid phosphonoxy)phenyl]propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 10 N 1 O 5 P 1 +</Formula>
-<Weight type="chemical">243.15 +</Weight>
-<Weight type="physical">243.029659 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0019">
-<Formula>C 0 H 1 N 0 O 3 P 1 +</Formula>
-<Weight type="chemical">79.98 +</Weight>
-<Weight type="physical">79.966331 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>van Mansfeld, A.D.M.</Author>
-<Author>van Teeffelen, H.A.A.M.</Author>
-<Author>Baas, P.D.</Author>
-<Author>Jansz, H.S.</Author>
-</Authors>
-<Citation>Nucleic Acids Res. 14, 4229-4238, 1986</Citation>
-<Title>Two juxtaposed tyrosyl-OH groups participate in phi X174 gene A protein catalysed cleavage and ligation of DNA.</Title>
-<Xref>DOI:10.1093/nar/14.10.4229</Xref>
-<Xref>PMID:2940511</Xref>
-<Note>isotope labeling</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hsieh, J.C.</Author>
-<Author>Jung, G.H.</Author>
-<Author>Leavitt, M.C.</Author>
-<Author>Ito, J.</Author>
-</Authors>
-<Citation>Nucleic Acids Res. 15, 8999-9009, 1987</Citation>
-<Title>Primary structure of the DNA terminal protein of bacteriophage PRD1.</Title>
-<Xref>DOI:10.1093/nar/15.21.8999</Xref>
-<Xref>PMID:3684578</Xref>
-<Note>structure prediction</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Shiue, S.Y.</Author>
-<Author>Hsieh, J.C.</Author>
-<Author>Ito, J.</Author>
-</Authors>
-<Citation>Nucleic Acids Res. 19, 3805-3810, 1991</Citation>
-<Title>Mapping of the DNA linking tyrosine residue of the PRD1 terminal protein.</Title>
-<Xref>DOI:10.1093/nar/19.14.3805</Xref>
-<Xref>PMID:1861973</Xref>
-<Note>directed mutation analysis</Note>
-</ReferenceBlock>
-<Comment>The keyword "phosphoprotein" is not used with polynucleotide-linked intermediate modifications.</Comment>
-<SequenceCode>
-<SequenceSpec>Y</SequenceSpec>
-<Xref>GO:0018163</Xref>
-<Xref>PSI-MOD:00259</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>*phosphoprotein</Keyword>
-<Keyword>genome-linked protein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="act_site__o-(5'-phospho-dna)-tyrosine intermediate__y">ACT_SITE O-(5'-phospho-DNA)-tyrosine intermediate</Feature>
-<Feature type="UniProt" key="mod_res__o-(5'-phospho-dna)-tyrosine__y">MOD_RES O-(5'-phospho-DNA)-tyrosine</Feature>
-</Features>
-<Image src="/images/AA0254.GIF" alt="DUMMY.GIF" />
-</Entry>
-<Entry id="AA0255">
-<Header>
-<Code>AA0255</Code>
-<Dates>
-<CreationDate>05-Jun-1998</CreationDate>
-<StrucRevDate>05-Jun-1998</StrucRevDate>
-<TextChngDate>30-Apr-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-(phospho-5'-DNA)-L-threonine</Name>
-<AlternateName>O3-(phospho-5'-DNA)-L-threonine</AlternateName>
-<AlternateName>O3-L-threonine 5'-DNA phosphodiester</AlternateName>
-<SystematicName>(S)-2-amino-3-(5'-deoxyribonucleic acid phosphonoxy)butanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 7 N 1 O 5 P 1 +</Formula>
-<Weight type="chemical">180.08 +</Weight>
-<Weight type="physical">180.006184 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0017">
-<Formula>C 0 H 0 N 0 O 3 P 1 +</Formula>
-<Weight type="chemical">78.97 +</Weight>
-<Weight type="physical">78.958505 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Garcia, P.</Author>
-<Author>Hermoso, J.M.</Author>
-<Author>Garcia, J.A.</Author>
-<Author>Garcia, E.</Author>
-<Author>Lopez, R.</Author>
-<Author>Salas, M.</Author>
-</Authors>
-<Citation>J. Virol. 58, 31-35, 1986</Citation>
-<Title>Formation of a covalent complex between the terminal protein of pneumococcal bacteriophage Cp-1 and 5'-dAMP.</Title>
-<Xref>PMID:3081736</Xref>
-<Note>chemical characterization</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>T</SequenceSpec>
-<Xref>GO:0018164</Xref>
-<Xref>PSI-MOD:00260</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>genome-linked protein</Keyword>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0255.GIF" alt="DUMMY.GIF" />
-</Entry>
-<Entry id="AA0256">
-<Header>
-<Code>AA0256</Code>
-<Dates>
-<CreationDate>11-Sep-1998</CreationDate>
-<StrucRevDate>11-Sep-1998</StrucRevDate>
-<TextChngDate>30-Sep-2008</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O4'-(phospho-5'-uridine)-L-tyrosine</Name>
-<AlternateName>5'-uridylic-O-tyrosine</AlternateName>
-<AlternateName>hydrogen 5'-uridylate tyrosine ester</AlternateName>
-<AlternateName>O4'-L-tyrosine 5'-uridine phosphodiester</AlternateName>
-<SystematicName>(S)-2-amino-3-[4-(5'-uridine phosphonoxy)phenyl]propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 18 H 20 N 3 O 10 P 1</Formula>
-<Weight type="chemical">469.34</Weight>
-<Weight type="physical">469.088630</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0019">
-<Formula>C 9 H 11 N 2 O 8 P 1</Formula>
-<Weight type="chemical">306.17</Weight>
-<Weight type="physical">306.025302</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Son, H.S.</Author>
-<Author>Rhee, S.G.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 262, 8690-8695, 1987</Citation>
-<Title>Cascade control of Escherichia coli glutamine synthetase: purification and properties of P-II protein and nucleotide sequence of its structural gene.</Title>
-<Xref>PMID:2885322</Xref>
-<Note>chemical detection and spectrographic characterization</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>uridylyltransferase (EC 2.7.7.59)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>Y</SequenceSpec>
-<Xref>GO:0018165</Xref>
-<Xref>PSI-MOD:00261</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__o-ump-tyrosine__y">MOD_RES O-UMP-tyrosine</Feature>
-</Features>
-<Image src="/images/AA0256.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0256.PDB" />
-</Entry>
-<Entry id="AA0257">
-<Header>
-<Code>AA0257</Code>
-<Dates>
-<CreationDate>11-Sep-1998</CreationDate>
-<StrucRevDate>31-Dec-2012</StrucRevDate>
-<TextChngDate>31-Dec-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-glutamyl L-tyrosine</Name>
-<AlternateName>N-(L-glutamyl)-L-tyrosine</AlternateName>
-<SystematicName>(S,S)-2-(2-aminopentanedio-1-yl)amino-3-(4-hydoxyphenyl)propanoic acid</SystematicName>
-<Xref>ChEBI:21477</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 14 H 17 N 2 O 6</Formula>
-<Weight type="chemical">309.30</Weight>
-<Weight type="physical">309.108661</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0006">
-<Formula>C 9 H 9 N 1 O 2</Formula>
-<Weight type="chemical">163.18</Weight>
-<Weight type="physical">163.063329</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Flavin, M.</Author>
-<Author>Murofushi, H.</Author>
-</Authors>
-<Citation>Meth. Enzymol. 106, 223-237, 1984</Citation>
-<Title>Tyrosine incorporation in tubulin.</Title>
-<Xref>DOI:10.1016/0076-6879(84)06024-9</Xref>
-<Xref>PMID:6387372</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ersfeld, K.</Author>
-<Author>Wehland, J.</Author>
-<Author>Plessmann, U.</Author>
-<Author>Dodemont, H.</Author>
-<Author>Gerke, V.</Author>
-<Author>Weber, K.</Author>
-</Authors>
-<Citation>J. Cell Biol. 120, 725-732, 1993</Citation>
-<Title>Characterization of the tubulin-tyrosine ligase.</Title>
-<Xref>DOI:10.1083/jcb.120.3.725</Xref>
-<Xref>PMID:8093886</Xref>
-<Note>biosynthesis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Xiao, H.</Author>
-<Author>El Bissati, K.</Author>
-<Author>Verdier-Pinard, P.</Author>
-<Author>Burd, B.</Author>
-<Author>Zhang, H.</Author>
-<Author>Kim, K.</Author>
-<Author>Fiser, A.</Author>
-<Author>Angeletti, R.H.</Author>
-<Author>Weiss, L.M.</Author>
-</Authors>
-<Citation>J. Proteome Res. 9, 359-372, 2010</Citation>
-<Title>Post-translational modifications to Toxoplasma gondii α- and β-tubulins include novel C-terminal methylation.</Title>
-<Xref>DOI:10.1021/pr900699a</Xref>
-<Xref>PMID:19886702</Xref>
-<Note>detection by mass-spectrometry in reflector mode</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>tubulin--tyrosine ligase (EC 6.3.2.25)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>E</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0018166</Xref>
-<Xref>PSI-MOD:00262</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="site__involved in polymerization__y">SITE Involved in polymerization</Feature>
-</Features>
-<Image src="/images/AA0257.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0257.PDB" />
-</Entry>
-<Entry id="AA0258">
-<Header>
-<Code>AA0258</Code>
-<Dates>
-<CreationDate>30-Sep-1999</CreationDate>
-<StrucRevDate>30-Sep-1999</StrucRevDate>
-<TextChngDate>29-Oct-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-phycoviolobilin-L-cysteine</Name>
-<AlternateName>cryptobiliviolin</AlternateName>
-<AlternateName>cryptoviolin</AlternateName>
-<AlternateName>cryptoviolobilin</AlternateName>
-<AlternateName>PBV</AlternateName>
-<AlternateName>PVB</AlternateName>
-<AlternateName>PXB</AlternateName>
-<AlternateName>S-phycobiliviolin-L-cysteine</AlternateName>
-<SystematicName>(4S)-3-[(1R)-1-(((2R)-2-amino-2-carboxy)ethylsulfanyl)ethyl]-8,12-bis(2-carboxyethyl)-18-ethyl-4,5-dihydro-2,7,13,17-tetramethyl-(21H,22H,24H)-biladiene-bc-1,19-dione</SystematicName>
-<Xref>CAS:124861-40-1</Xref>
-<Xref>COMe:BIM000254</Xref>
-<Xref>PDBHET:PVN</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 36 H 43 N 5 O 7 S 1</Formula>
-<Weight type="chemical">689.83</Weight>
-<Weight type="physical">689.288320</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 33 H 38 N 4 O 6 S 0</Formula>
-<Weight type="chemical">586.69</Weight>
-<Weight type="physical">586.279135</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bishop, J.E.</Author>
-<Author>Rapoport, H.</Author>
-<Author>Klotz, A.V.</Author>
-<Author>Chan, C.F.</Author>
-<Author>Glazer, A.N.</Author>
-<Author>Fueglistaller, P.</Author>
-<Author>Zuber, H.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 109, 875-881, 1987</Citation>
-<Title>Chromopeptides from phycoerythrocyanin. Structure and linkage of the three bilin groups.</Title>
-<Xref>DOI:10.1021/ja00237a039</Xref>
-<Note>spectrographic characterization; mass spectrometric and (1)H-NMR identification; peptide linkage</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Moss, G.P.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 178, 277-328, 1988</Citation>
-<Title>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN). Nomenclature of tetrapyrroles. Recommendations 1986.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1988.tb14453.x</Xref>
-<Xref>PMID:3208761</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Duerring, M.</Author>
-<Author>Huber, R.</Author>
-<Author>Bode, W.</Author>
-<Author>Ruembeli, R.</Author>
-<Author>Zuber, H.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 211, 633-644, 1990</Citation>
-<Title>Refined three-dimensional structure of phycoerythrocyanin from the cyanobacterium Mastigocladus laminosus at 2.7 A.</Title>
-<Xref>DOI:10.1016/0022-2836(90)90270-V</Xref>
-<Xref>PMID:2106585</Xref>
-<Note>X-ray diffraction, 2.7 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Zhao, K.H.</Author>
-<Author>Deng, M.G.</Author>
-<Author>Zheng, M.</Author>
-<Author>Zhou, M.</Author>
-<Author>Parbel, A.</Author>
-<Author>Storf, M.</Author>
-<Author>Meyer, M.</Author>
-<Author>Strohmann, B.</Author>
-<Author>Scheer, H.</Author>
-</Authors>
-<Citation>FEBS Lett. 469, 9-13, 2000</Citation>
-<Title>Novel activity of a phycobiliprotein lyase: both the attachment of phycocyanobilin and the isomerization to phycoviolobilin are catalyzed by the proteins PecE and PecF encoded by the phycoerythrocyanin operon.</Title>
-<Xref>DOI:10.1016/S0014-5793(00)01245-X</Xref>
-<Xref>PMID:10708746</Xref>
-</ReferenceBlock>
-<Comment>The phycoviolobilins transmit violet.</Comment>
-<Comment>It has not been established whether the chromophores that have been referred to as cryptoviolins have the same structure as phycoviolobilin.</Comment>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>GO:0017008</Xref>
-<Xref>GO:0018356</Xref>
-<Xref>PSI-MOD:00263</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chromoprotein</Keyword>
-<Keyword>phycoviolobilin</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="binding__phycoviolobilin chromophore (covalent; via 1 link)__c">BINDING Phycoviolobilin chromophore (covalent; via 1 link)</Feature>
-</Features>
-<Image src="/images/AA0258.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0258.PDB" />
-</Entry>
-<Entry id="AA0259">
-<Header>
-<Code>AA0259</Code>
-<Dates>
-<CreationDate>30-Sep-1999</CreationDate>
-<StrucRevDate>30-Sep-1999</StrucRevDate>
-<TextChngDate>30-Sep-2008</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>phycoerythrobilin-bis-L-cysteine</Name>
-<AlternateName>3,18-bis-[1-((2-amino-2-carboxy)ethylsulfanyl)ethyl]-2,3,15,16-tetrahydro-2,7,13,17-tetramethyl-1,19-dioxo-(21H,22H,24H)-biladiene-ab-8,12-dipropanoic acid</AlternateName>
-<AlternateName>PEB</AlternateName>
-<AlternateName>phycoerythrobilin biscysteine adduct</AlternateName>
-<SystematicName>(2S,3R,16R)-3,18-bis-[(R)-1-(((2R)-2-amino-2-carboxy)ethylsulfanyl)ethyl]-8,12-bis(2-carboxyethyl)-2,7,13,17-tetramethyl-2,3,15,16-tetrahydrobilin-1,19(21H,22H,24H)-dione</SystematicName>
-<Xref>CAS:18097-67-1</Xref>
-<Xref>COMe:BIM000150</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 39 H 48 N 6 O 8 S 2</Formula>
-<Weight type="chemical">792.97</Weight>
-<Weight type="physical">792.297505</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005">
-<Formula>C 33 H 38 N 4 O 6 S 0</Formula>
-<Weight type="chemical">586.69</Weight>
-<Weight type="physical">586.279135</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Nagy, J.O.</Author>
-<Author>Bishop, J.E.</Author>
-<Author>Klotz, A.V.</Author>
-<Author>Glazer, A.N.</Author>
-<Author>Rapoport, H.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 260, 4864-4868, 1985</Citation>
-<Title>Bilin attachment sites in the alpha, beta, and gamma subunits of R-phycoerythrin. Structural studies on singly and doubly linked phycourobilins.</Title>
-<Xref>PMID:3838747</Xref>
-<Note>mass spectrometric and (1)H-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Moss, G.P.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 178, 277-328, 1988</Citation>
-<Title>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN). Nomenclature of tetrapyrroles. Recommendations 1986.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1988.tb14453.x</Xref>
-<Xref>PMID:3208761</Xref>
-</ReferenceBlock>
-<Comment>There are additional chiral centers at C-2, C-3, and C-16.</Comment>
-<Comment>The phytochromobilins and phycoerythrobilins transmit red.</Comment>
-<SequenceCode>
-<SequenceSpec>C, C</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>GO:0017011</Xref>
-<Xref>GO:0018167</Xref>
-<Xref>PSI-MOD:00264</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chromoprotein</Keyword>
-<Keyword>phycoerythrobilin</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="binding__phycoerythrobilin chromophore (covalent; via 2 links)__c__c">BINDING Phycoerythrobilin chromophore (covalent; via 2 links)</Feature>
-</Features>
-<Image src="/images/AA0259.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0259.PDB" />
-</Entry>
-<Entry id="AA0260">
-<Header>
-<Code>AA0260</Code>
-<Dates>
-<CreationDate>30-Sep-1999</CreationDate>
-<StrucRevDate>08-Jun-2001</StrucRevDate>
-<TextChngDate>20-May-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>phycourobilin-bis-L-cysteine</Name>
-<AlternateName>3,18-bis(1-[(R)-2-amino-2-carboxyethyl]sulfanylethyl)-2,7,13,17-tetramethyl-1,19-dioxo-4,5,15,16-tetrahydro-(21H,22H,24H)-bilene-b-8,12-dipropanoic acid</AlternateName>
-<AlternateName>phycourobilin biscysteine adduct</AlternateName>
-<AlternateName>PUB</AlternateName>
-<SystematicName>3,18-bis(1-[(R)-2-amino-2-carboxyethyl]sulfanylethyl)-8,12-bis(2-carboxyethyl)-2,7,13,17-tetramethyl-4,5,15,16-tetrahydro-(21H,22H,24H)-bilene-b-1,19(4H,16H)-dione</SystematicName>
-<Xref>CAS:61932-71-6</Xref>
-<Xref>COMe:BIM000146</Xref>
-<Xref>PDBHET:PUB</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 39 H 48 N 6 O 8 S 2</Formula>
-<Weight type="chemical">792.97</Weight>
-<Weight type="physical">792.297505</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005">
-<Formula>C 33 H 38 N 4 O 6 S 0</Formula>
-<Weight type="chemical">586.69</Weight>
-<Weight type="physical">586.279135</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Nagy, J.O.</Author>
-<Author>Bishop, J.E.</Author>
-<Author>Klotz, A.V.</Author>
-<Author>Glazer, A.N.</Author>
-<Author>Rapoport, H.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 260, 4864-4868, 1985</Citation>
-<Title>Bilin attachment sites in the alpha, beta, and gamma subunits of R-phycoerythrin. Structural studies on singly and doubly linked phycourobilins.</Title>
-<Xref>PMID:3838747</Xref>
-<Note>mass spectrometric and (1)H-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Killilea, S.D.</Author>
-<Author>O'Carra, P.</Author>
-</Authors>
-<Citation>Biochem. J. 226, 723-731, 1985</Citation>
-<Title>Structure and apoprotein linkages of phycourobilin.</Title>
-<Xref>PMID:3838665</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Moss, G.P.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 178, 277-328, 1988</Citation>
-<Title>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN). Nomenclature of tetrapyrroles. Recommendations 1986.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1988.tb14453.x</Xref>
-<Xref>PMID:3208761</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Chang, W.R.</Author>
-<Author>Jiang, T.</Author>
-<Author>Wan, Z.L.</Author>
-<Author>Zhang, J.P.</Author>
-<Author>Yang, Z.X.</Author>
-<Author>Liang, D.C.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 262, 721-731, 1996</Citation>
-<Title>Crystal structure of R-phycoerythrin from Polysiphonia urceolata at 2.8 angstroms resolution.</Title>
-<Xref>DOI:10.1006/jmbi.1996.0547</Xref>
-<Xref>PMID:8876649</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Liang, D.C.</Author>
-<Author>Jiang, T.</Author>
-<Author>Chang, W.R.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, January 1996</Citation>
-<Description>Crystal structure of R-phycoerythrin from Polysiphonia at 2.8 A resolution.</Description>
-<Xref>PDB:1LIA</Xref>
-</ReferenceBlock>
-<Comment>There are additional chiral centers at C-3alpha, C-4, C-16 and C-18alpha.</Comment>
-<SequenceCode>
-<SequenceSpec>C, C</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>GO:0017010</Xref>
-<Xref>GO:0018357</Xref>
-<Xref>PSI-MOD:00265</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chromoprotein</Keyword>
-<Keyword>phycourobilin</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="binding__phycourobilin chromophore (covalent; via 2 links)__c__c">BINDING Phycourobilin chromophore (covalent; via 2 links)</Feature>
-</Features>
-<Image src="/images/AA0260.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0260.PDB" />
-</Entry>
-<Entry id="AA0261">
-<Header>
-<Code>AA0261</Code>
-<Dates>
-<CreationDate>11-Sep-1998</CreationDate>
-<StrucRevDate>31-Dec-2012</StrucRevDate>
-<TextChngDate>31-Dec-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-(L-glutamyl)-poly-L-glutamic acid</Name>
-</Names>
-<FormulaBlock>
-<Formula>C 10 H 15 N 2 O 7 +</Formula>
-<Weight type="chemical">275.24 +</Weight>
-<Weight type="physical">275.087926 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0006">
-<Formula>C 5 H 7 N 1 O 3 +</Formula>
-<Weight type="chemical">129.12 +</Weight>
-<Weight type="physical">129.042593 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hitz, H.</Author>
-<Author>Schäfer, D.</Author>
-<Author>Wittmann-Liebold, B.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 75, 497-512, 1977</Citation>
-<Title>Determination of the complete amino-acid sequence of protein S6 from the wild-type and a mutant of Escherichia coli.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1977.00497.pp.x</Xref>
-<Xref>PMID:328274</Xref>
-<Note>five forms of the protein, which differ only in the number of carboxyl-terminal glutamic acid residues, were isolated and sequenced</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kang, W.K.</Author>
-<Author>Icho, T.</Author>
-<Author>Isono, S.</Author>
-<Author>Kitakawa, M.</Author>
-<Author>Isono, K.</Author>
-</Authors>
-<Citation>Mol. Gen. Genet. 217, 281-288, 1989</Citation>
-<Title>Characterization of the gene rimK responsible for the addition of glutamic acid residues to the C-terminus of ribosomal protein S6 in Escherichia coli K12.</Title>
-<Xref>DOI:10.1007/BF02464894</Xref>
-<Xref>PMID:2570347</Xref>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>ribosomal S6--glutamic acid ligase (EC 6.3.2.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>E</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0018170</Xref>
-<Xref>PSI-MOD:00266</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">CHAIN 30S ribosomal protein S6, fully modified isoform</Feature>
-<Note>this is not annotated as a modification in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0261.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0261.PDB" />
-</Entry>
-<Entry id="AA0262">
-<Header>
-<Code>AA0262</Code>
-<Dates>
-<CreationDate>30-Sep-1999</CreationDate>
-<StrucRevDate>30-Sep-1999</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-cysteine sulfinic acid</Name>
-<AlternateName>2-amino-2-carboxyethanesulfinic acid</AlternateName>
-<AlternateName>2-amino-3-(dioxido-lambda(6)-sulfanyl)propanoic acid [tautomer]</AlternateName>
-<AlternateName>2-amino-3-sulfonylpropanoic acid [tautomer]</AlternateName>
-<AlternateName>3-sulfinoalanine</AlternateName>
-<AlternateName>3-sulphinoalanine</AlternateName>
-<AlternateName>cysteine sulphinic acid</AlternateName>
-<AlternateName>cysteine-S,S-dioxide [tautomer]</AlternateName>
-<AlternateName>S-cysteinesulfinic acid</AlternateName>
-<AlternateName>S-hydroxy-S-oxo-L-cysteine residue </AlternateName>
-<AlternateName>S-sulfinocysteine</AlternateName>
-<SystematicName>(2R)-2-amino-3-sulfinopropanoic acid</SystematicName>
-<Xref>CAS:1115-65-7</Xref>
-<Xref>CAS:2381-08-0</Xref>
-<Xref>ChEBI:61964</Xref>
-<Xref>ChEBI:61967</Xref>
-<Xref>PDBHET:CSD</Xref>
-<Xref>PDBHET:CSW</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 5 N 1 O 3 S 1</Formula>
-<Weight type="chemical">135.14</Weight>
-<Weight type="physical">134.999014</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 0 H 0 N 0 O 2 S 0</Formula>
-<Weight type="chemical">32.00</Weight>
-<Weight type="physical">31.989829</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Nagashima, S.</Author>
-<Author>Nakasako, M.</Author>
-<Author>Dohmae, N.</Author>
-<Author>Tsujimura, M.</Author>
-<Author>Takio, K.</Author>
-<Author>Odaka, M.</Author>
-<Author>Yohda, M.</Author>
-<Author>Kamiya, N.</Author>
-<Author>Endo, I.</Author>
-</Authors>
-<Citation>Nature Struct. Biol. 5, 347-351, 1998</Citation>
-<Title>Novel non-heme iron center of nitrile hydratase with a claw setting of oxygen atoms.</Title>
-<Xref>DOI:10.1038/nsb0598-347</Xref>
-<Xref>PMID:9586994</Xref>
-<Note>X-ray diffraction, 1.7 angstroms; mass spectroscopic identification</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>GO:0018171</Xref>
-<Xref>GO:0018323</Xref>
-<Xref>PSI-MOD:00267</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="act_site__redox-active__c">ACT_SITE Redox-active</Feature>
-<Feature type="UniProt" key="mod_res__cysteine sulfinic acid (-so2h)__c">MOD_RES Cysteine sulfinic acid (-SO2H)</Feature>
-</Features>
-<Image src="/images/AA0262.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0262.PDB" />
-</Entry>
-<Entry id="AA0263">
-<Header>
-<Code>AA0263</Code>
-<Dates>
-<CreationDate>30-Sep-1999</CreationDate>
-<StrucRevDate>30-Sep-1999</StrucRevDate>
-<TextChngDate>24-Oct-2008</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-3',4',5'-trihydroxyphenylalanine</Name>
-<AlternateName>L-3,4,5-TOPA</AlternateName>
-<SystematicName>(S)-2-amino-3-(3,4,5-trihydroxyphenyl)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 9 N 1 O 4</Formula>
-<Weight type="chemical">195.17</Weight>
-<Weight type="physical">195.053158</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0019">
-<Formula>C 0 H 0 N 0 O 2</Formula>
-<Weight type="chemical">32.00</Weight>
-<Weight type="physical">31.989829</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Taylor, S.W.</Author>
-<Author>Ross, M.M.</Author>
-<Author>Waite, J.H.</Author>
-</Authors>
-<Citation>Arch. Biochem. Biophys. 324, 228-240, 1995</Citation>
-<Title>Novel 3,4-di- and 3,4,5-trihydroxyphenylalanine-containing polypeptides from the blood cells of the ascidians Ascidia ceratodes and Molgula manhattensis.</Title>
-<Xref>DOI:10.1006/abbi.1995.0035</Xref>
-<Xref>PMID:8554314</Xref>
-<Note>chromatographic and mass spectrometric detection; (1)H-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Taylor, S.W.</Author>
-<Author>Kammerer, B.</Author>
-<Author>Nicholson, G.J.</Author>
-<Author>Pusecker, K.</Author>
-<Author>Walk, T.</Author>
-<Author>Bayer, E.</Author>
-<Author>Scippa, S.</Author>
-<Author>de Vincentiis, M.</Author>
-</Authors>
-<Citation>Arch. Biochem. Biophys. 348, 278-288, 1997</Citation>
-<Title>Morulin Pm: a modified polypeptide containing TOPA and 6-bromotryptophan from the morula cells of the ascidian, Phallusia mammillata.</Title>
-<Xref>DOI:10.1006/abbi.1997.0371</Xref>
-<Xref>PMID:9434739</Xref>
-<Note>(1)H-NMR and (13)C-NMR characterization</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>Y</SequenceSpec>
-<Xref>GO:0018172</Xref>
-<Xref>PSI-MOD:00268</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0263.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0263.PDB" />
-</Entry>
-<Entry id="AA0264">
-<Header>
-<Code>AA0264</Code>
-<Dates>
-<CreationDate>04-Dec-1998</CreationDate>
-<StrucRevDate>04-Dec-1998</StrucRevDate>
-<TextChngDate>31-Mar-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-(sn-1-glycerophosphoryl)-L-serine</Name>
-<AlternateName>alpha-glycerophosphoryl serine</AlternateName>
-<AlternateName>glycerophosphoserine</AlternateName>
-<AlternateName>O3-(sn-1-glycerophosphoryl)-L-serine</AlternateName>
-<AlternateName>O3-2,3-dihydroxypropyl hydrogen phosphate-L-serine ester</AlternateName>
-<AlternateName>O3-L-serine glyceryl-1-phosphodiester</AlternateName>
-<SystematicName>(2S)-2-amino-3-[(2Xi)-2,3-dihydroxypropyl]phosphonoxypropanoic acid</SystematicName>
-<Xref>CAS:26289-09-8</Xref>
-<Xref>PDBHET:OPE</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 12 N 1 O 7 P 1</Formula>
-<Weight type="chemical">241.14</Weight>
-<Weight type="physical">241.035138</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 3 H 7 N 0 O 5 P 1</Formula>
-<Weight type="chemical">154.06</Weight>
-<Weight type="physical">154.003110</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Stimson, E.</Author>
-<Author>Virji, M.</Author>
-<Author>Barker, S.</Author>
-<Author>Panico, M.</Author>
-<Author>Blench, I.</Author>
-<Author>Saunders, J.</Author>
-<Author>Payne, G.</Author>
-<Author>Moxon, E.R.</Author>
-<Author>Dell, A.</Author>
-<Author>Morris, H.R.</Author>
-</Authors>
-<Citation>Biochem. J. 316, 29-33, 1996</Citation>
-<Title>Discovery of a novel protein modification: alpha-glycerophosphate is a substituent of meningococcal pilin.</Title>
-<Xref>PMID:8645220</Xref>
-<Note>mass spectrometric identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Forest, K.T.</Author>
-<Author>Dunham, S.A.</Author>
-<Author>Koomey, M.</Author>
-<Author>Tainer, J.A.</Author>
-</Authors>
-<Citation>Mol. Microbiol. 31, 743-752, 1999</Citation>
-<Title>Crystallographic structure reveals phosphorylated pilin from Neisseria: phosphoserine sites modify type IV pilus surface chemistry and fibre morphology.</Title>
-<Xref>DOI:10.1046/J.1365-2958.1999.01184.X</Xref>
-<Xref>PMID:10048019</Xref>
-<Note>X-ray diffraction, 2.60 angstroms; density was observed at the predicted position of the phosphoryl group, but was too low to model due to low occupancy or disorder</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Chamot-Rooke, J.</Author>
-<Author>Mikaty, G.</Author>
-<Author>Malosse, C.</Author>
-<Author>Soyer, M.</Author>
-<Author>Dumont, A.</Author>
-<Author>Gault, J.</Author>
-<Author>Imhaus, A.F.</Author>
-<Author>Martin, P.</Author>
-<Author>Trellet, M.</Author>
-<Author>Clary, G.</Author>
-<Author>Chafey, P.</Author>
-<Author>Camoin, L.</Author>
-<Author>Nilges, M.</Author>
-<Author>Nassif, X.</Author>
-<Author>Duménil, G.</Author>
-</Authors>
-<Citation>Science 331, 778-782, 2011</Citation>
-<Title>Posttranslational modification of pili upon cell contact triggers N. meningitidis dissemination.</Title>
-<Xref>DOI:10.1126/science.1200729</Xref>
-<Xref>PMID:21311024</Xref>
-<Note>mass spectrometric detection; directed mutation analysis</Note>
-</ReferenceBlock>
-<Comment>The stereochemistry of the glycerol phosphate has not been determined. The sn-1 form is assumed.</Comment>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>GO:0018340</Xref>
-<Xref>PSI-MOD:00269</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__o-(sn-1-glycerophosphoryl)serine__s">MOD_RES O-(sn-1-glycerophosphoryl)serine</Feature>
-</Features>
-<Image src="/images/AA0264.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0264.PDB" />
-</Entry>
-<Entry id="AA0265">
-<Header>
-<Code>AA0265</Code>
-<Dates>
-<CreationDate>30-Apr-1999</CreationDate>
-<StrucRevDate>30-Apr-1999</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>1-thioglycine</Name>
-<AlternateName>2-amino-1-sulfanylethanone</AlternateName>
-<AlternateName link="INT">aminoethanethioic O-acid</AlternateName>
-<AlternateName link="CTER">aminoethanethioic S-acid</AlternateName>
-<AlternateName link="CTER">aminoethanethiolic acid</AlternateName>
-<AlternateName link="INT">aminoethanethionic acid</AlternateName>
-<AlternateName>aminothioacetic acid</AlternateName>
-<SystematicName>aminoethanethioic acid</SystematicName>
-<Xref>CAS:758-10-1</Xref>
-<Xref>PDBHET:GL3</Xref>
-</Names>
-<FormulaBlock label="INT">
-<Formula>C 2 H 3 N 1 O 0 S 1</Formula>
-<Weight type="chemical">73.11</Weight>
-<Weight type="physical">72.998620</Weight>
-</FormulaBlock>
-<FormulaBlock label="CTER">
-<Formula>C 2 H 4 N 1 O 1 S 1</Formula>
-<Weight type="chemical">90.12</Weight>
-<Weight type="physical">90.001360</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0008" link="INT">
-<Formula>C 0 H 0 N 0 O -1 S 1</Formula>
-<Weight type="chemical">16.06</Weight>
-<Weight type="physical">15.977156</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0008" link="CTER">
-<Formula>C 0 H 0 N 0 O -1 S 1</Formula>
-<Weight type="chemical">16.06</Weight>
-<Weight type="physical">15.977156</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ermler, U.</Author>
-<Author>Grabarse, W.</Author>
-<Author>Shima, S.</Author>
-<Author>Goubeaud, M.</Author>
-<Author>Thauer, R.K.</Author>
-</Authors>
-<Citation>Science 278, 1457-1462, 1997</Citation>
-<Title>Crystal structure of methyl-coenzyme M reductase: the key enzyme of biological methane formation.</Title>
-<Xref>DOI:10.1126/science.278.5342.1457</Xref>
-<Xref>PMID:9367957</Xref>
-<Note>X-ray diffraction, 1.45 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Leimkuehler, S.</Author>
-<Author>Wuebbens, M.M.</Author>
-<Author>Rajagopalan, K.V.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 276, 34695-34701, 2001</Citation>
-<Title>Characterization of Escherichia coli MoeB and its involvement in the activation of molybdopterin synthase for the biosynthesis of the molybdenum cofactor.</Title>
-<Xref>DOI:10.1074/jbc.M102787200</Xref>
-<Xref>PMID:11463785</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Leidel, S.</Author>
-<Author>Pedrioli, P.G.</Author>
-<Author>Bucher, T.</Author>
-<Author>Brost, R.</Author>
-<Author>Costanzo, M.</Author>
-<Author>Schmidt, A.</Author>
-<Author>Aebersold, R.</Author>
-<Author>Boone, C.</Author>
-<Author>Hofmann, K.</Author>
-<Author>Peter, M.</Author>
-</Authors>
-<Citation>Nature 458, 228-232, 2009</Citation>
-<Title>Ubiquitin-related modifier Urm1 acts as a sulphur carrier in thiolation of eukaryotic transfer RNA.</Title>
-<Xref>DOI:10.1038/nature07643</Xref>
-<Xref>PMID:19145231</Xref>
-</ReferenceBlock>
-<Comment>As a peptide this may exist predominantly in the iminyl-thiol [-C(SH)=N-] tautomeric form.</Comment>
-<Comment>See also RESID:AA0206.</Comment>
-<Comment>The formula and records labeled "INT" refers to thioglycine occurring as an internal residue with a thioamide peptide bond.</Comment>
-<Comment>The formula and records labeled "CTER" refers to thioglycine occurring as a carboxyl end residue.</Comment>
-<SequenceCode link="INT">
-<SequenceSpec>G</SequenceSpec>
-<Xref>GO:0018173</Xref>
-<Xref>GO:0019920</Xref>
-<Xref>PSI-MOD:00270</Xref>
-</SequenceCode>
-<SequenceCode link="CTER">
-<SequenceSpec>G</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0018173</Xref>
-<Xref>GO:0019921</Xref>
-<Xref>PSI-MOD:01623</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>thiopeptide bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__1-thioglycine__g">MOD_RES 1-thioglycine</Feature>
-</Features>
-<Image src="/images/AA0265.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0265.PDB" />
-</Entry>
-<Entry id="AA0266">
-<Header>
-<Code>AA0266</Code>
-<Dates>
-<CreationDate>30-Apr-1999</CreationDate>
-<StrucRevDate>31-Dec-2009</StrucRevDate>
-<TextChngDate>31-Dec-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>heme P460-bis-L-cysteine-L-tyrosine</Name>
-<AlternateName>bis(S-cysteinyl)-(tyros-3'-yl)-heme</AlternateName>
-<SystematicName>(10S,11S)-[7,12-bis((S)-1-[((R)-2-amino-2-carboxy)ethylsulfanyl]ethyl)-10-(2-hydroxy-5-[(S)-2-amino-2-carboxy]ethylphenyl)-3,8,13,17-tetramethyl-21H,23H-10,11-dihydroporphine-2,18-bis(2-carboxyethyl)-N21,N22,N23,N24]-ferrate</SystematicName>
-<Xref>COMe:BIM000242</Xref>
-<Xref>PDBHET:HEC</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 49 Fe 1 H 51 N 7 O 8 S 2</Formula>
-<Weight type="chemical">985.95</Weight>
-<Weight type="physical">985.258991</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005 AA0019">
-<Formula>C 34 Fe 1 H 32 N 4 O 4 S 0</Formula>
-<Weight type="chemical">616.50</Weight>
-<Weight type="physical">616.177293</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Arciero, D.M.</Author>
-<Author>Hooper, A.B.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 268, 14645-14654, 1993</Citation>
-<Title>Hydroxylamine oxidoreductase from Nitrosomonas europaea is a multimer of an octa-heme subunit.</Title>
-<Xref>PMID:8325841</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Tanaka, N.</Author>
-<Author>Igarashi, N.</Author>
-<Author>Moriyama, H.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, March 1997</Citation>
-<Description>X-Ray structure of hydroxylamine oxidoreductase.</Description>
-<Xref>PDB:1FGJ</Xref>
-<Note>X-ray diffraction, 2.8 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Igarashi, N.</Author>
-<Author>Moriyama, H.</Author>
-<Author>Fujiwara, T.</Author>
-<Author>Fukumori, Y.</Author>
-<Author>Tanaka, N.</Author>
-</Authors>
-<Citation>Nature Struct. Biol. 4, 276-284, 1997</Citation>
-<Title>The 2.8 A structure of hydroxylamine oxidoreductase from a nitrifying chemoautotrophic bacterium, Nitrosomonas europaea.</Title>
-<Xref>DOI:10.1038/nsb0497-276</Xref>
-<Xref>PMID:9095195</Xref>
-<Note>X-ray diffraction, 2.8 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Pearson, A.R.</Author>
-<Author>Elmore, B.O.</Author>
-<Author>Yang, C.</Author>
-<Author>Ferrara, J.D.</Author>
-<Author>Hooper, A.B.</Author>
-<Author>Wilmot, C.M.</Author>
-</Authors>
-<Citation>Biochemistry 46, 8340-8349, 2007</Citation>
-<Title>The crystal structure of cytochrome P460 of Nitrosomonas europaea reveals a novel cytochrome fold and heme-protein cross-link.</Title>
-<Xref>DOI:10.1021/bi700086r</Xref>
-<Xref>PMID:17583915</Xref>
-<Note>an alternative structure is proposed for the tyrosyl-heme linkage based on the higher resolution structure obtained for a lysyl-heme linkage</Note>
-</ReferenceBlock>
-<Comment>The diagram has been corrected for reduction of the protoporphyrin C10-C11 bond. A corrected model is not available.</Comment>
-<Comment>A mechanism for free radical reductive addition is not provided by the authors of the proposed structure, and the alternative structure with a tyrosyl-O linkage seems more plausible. See RESID:AA0271.</Comment>
-<Comment>The heavy atom coordinates of the model are assigned according to the coordinates in PDB:1FDJ and the instructions for transformation given by the authors.</Comment>
-<SequenceCode>
-<SequenceSpec>C, C, Y</SequenceSpec>
-<Condition>cross-link 3</Condition>
-<Xref>GO:0018174</Xref>
-<Xref>GO:0018359</Xref>
-<Xref>PSI-MOD:00271</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chromoprotein</Keyword>
-<Keyword>heme</Keyword>
-<Keyword>iron</Keyword>
-<Keyword>metalloprotein</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="binding__heme (covalent; via 3 links)__y">BINDING Heme (covalent; via 3 links)</Feature>
-</Features>
-<Image src="/images/AA0266.GIF" alt="DUMMY.GIF" />
-</Entry>
-<Entry id="AA0267">
-<Header>
-<Code>AA0267</Code>
-<Dates>
-<CreationDate>30-Apr-1999</CreationDate>
-<StrucRevDate>30-Apr-1999</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-(phospho-5'-adenosine)-L-threonine</Name>
-<AlternateName>5'-adenylic-O3-L-threonine</AlternateName>
-<AlternateName>beta-5'-adenylic-L-threonine</AlternateName>
-<AlternateName>L-threonine monoanhydride with 5'-adenylic acid</AlternateName>
-<AlternateName>O(gamma)-5'-adenylic-L-threonine</AlternateName>
-<AlternateName>O3-(phospho-5'-adenosine)-L-threonine</AlternateName>
-<AlternateName>O3-L-threonine 5'-adenosine phosphodiester</AlternateName>
-<SystematicName>(2S,3R)-2-amino-3-(5'-adenosine phosphonoxy)butanoic acid</SystematicName>
-<Xref>ChEBI:138113</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 14 H 19 N 6 O 8 P 1</Formula>
-<Weight type="chemical">430.31</Weight>
-<Weight type="physical">430.100198</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0017">
-<Formula>C 10 H 12 N 5 O 6 P 1</Formula>
-<Weight type="chemical">329.21</Weight>
-<Weight type="physical">329.052520</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Culp, J.S.</Author>
-<Author>Blytt, H.J.</Author>
-<Author>Hermodson, M.</Author>
-<Author>Butler, L.G.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 260, 8320-8324, 1985</Citation>
-<Title>Amino acid sequence of the active site peptide of bovine intestinal 5'-nucleotide phosphodiesterase and identification of the active site residue as threonine.</Title>
-<Xref>PMID:2989287</Xref>
-<Note>radioisotope labeling</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Stefan, C.</Author>
-<Author>Stalmans, W.</Author>
-<Author>Bollen, M.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 241, 338-342, 1996</Citation>
-<Title>Threonine autophosphorylation and nucleotidylation of the hepatic membrane protein PC-1.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1996.00338.x</Xref>
-<Xref>PMID:8917428</Xref>
-<Note>radioisotope labeling; linkage analysis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yarbrough, M.L.</Author>
-<Author>Li, Y.</Author>
-<Author>Kinch, L.N.</Author>
-<Author>Grishin, N.V.</Author>
-<Author>Ball, H.L.</Author>
-<Author>Orth, K.</Author>
-</Authors>
-<Citation>Science 323, 269-272, 2009</Citation>
-<Title>AMPylation of Rho GTPases by Vibrio VopS disrupts effector binding and downstream signaling.</Title>
-<Xref>DOI:10.1126/science.1166382</Xref>
-<Xref>PMID:19039103</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kinch, L.N.</Author>
-<Author>Yarbrough, M.L.</Author>
-<Author>Orth, K.</Author>
-<Author>Grishin, N.V.</Author>
-</Authors>
-<Citation>PLoS One 4, e5818, 2009</Citation>
-<Title>Fido, a novel AMPylation domain common to fic, doc, and AvrB.</Title>
-<Xref>DOI:10.1371/journal.pone.0005818</Xref>
-<Xref>PMID:19503829</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Li, Y.</Author>
-<Author>Al-Eryani, R.</Author>
-<Author>Yarbrough, M.L.</Author>
-<Author>Orth, K.</Author>
-<Author>Ball, H.L.</Author>
-</Authors>
-<Citation>J. Am. Soc. Mass Spectrom. 22, 752-761, 2011</Citation>
-<Title>Characterization of AMPylation on Threonine, Serine, and Tyrosine Using Mass Spectrometry.</Title>
-<Xref>DOI:10.1007/s13361-011-0084-1</Xref>
-<Xref>PMID:21472612</Xref>
-<Note>mass spectrometric detection and characterization of tandem-MS fragmentation</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>T</SequenceSpec>
-<Xref>GO:0018178</Xref>
-<Xref>GO:0018332</Xref>
-<Xref>PSI-MOD:00272</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="act_site__amp-threonine intermediate__t">ACT_SITE AMP-threonine intermediate</Feature>
-<Feature type="UniProt" key="mod_res__o-amp-threonine__t">MOD_RES O-AMP-threonine</Feature>
-</Features>
-<Image src="/images/AA0267.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0267.PDB" />
-</Entry>
-<Entry id="AA0268">
-<Header>
-<Code>AA0268</Code>
-<Dates>
-<CreationDate>07-May-1999</CreationDate>
-<StrucRevDate>07-May-1999</StrucRevDate>
-<TextChngDate>31-Dec-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>tris-L-cysteinyl L-cysteine persulfido bis-L-glutamato L-histidino tetrairon disulfide trioxide</Name>
-<AlternateName>4Fe-2S-3O cluster</AlternateName>
-<AlternateName>hybrid four iron cluster 2</AlternateName>
-<AlternateName>prismane iron-sulfur cofactor [misnomer]</AlternateName>
-<SystematicName>mu-1:2kappaO-oxido-mu-1:3kappaO-oxido-mu-2:4kappaO-oxido-mu-3:4kappaS-sulfido-mu3-2:3:4kappaS-sulfido-S-cysteinyl-N1'-histidino-O5-glutamato 1-iron-S5-cysteine persulfido-O5-glutamato 2-iron-3,4-bis-(S-cysteinyl iron)</SystematicName>
-<Xref>COMe:BIM000058</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 28 Fe 4 H 34 N 9 O 14 S 7</Formula>
-<Weight type="chemical">1168.43</Weight>
-<Weight type="physical">1167.766769</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0009 AA0006 AA0005 AA0005 AA0005 AA0005 AA0006">
-<Formula>C 0 Fe 4 H -7 N 0 O 3 S 3</Formula>
-<Weight type="chemical">360.50</Weight>
-<Weight type="physical">360.585932</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Arendsen, A.F.</Author>
-<Author>Hadden, J.</Author>
-<Author>Card, G.</Author>
-<Author>McAlpine, A.S.</Author>
-<Author>Bailey, S.</Author>
-<Author>Zaitsev, V.</Author>
-<Author>Duke, E.H.M.</Author>
-<Author>Lindley, P.F.</Author>
-<Author>Kroeckel, M.</Author>
-<Author>Trautwein, A.X.</Author>
-<Author>Feiters, M.C.</Author>
-<Author>Charnock, J.M.</Author>
-<Author>Garner, C.D.</Author>
-<Author>Marritt, S.J.</Author>
-<Author>Thomson, A.J.</Author>
-<Author>Kooter, I.M.</Author>
-<Author>Johnson, M.K.</Author>
-<Author>van den Berg, W.A.M.</Author>
-<Author>van Dongen, W.M.A.M.</Author>
-<Author>Hagen, W.R.</Author>
-</Authors>
-<Citation>J. Biol. Inorg. Chem. 3, 81-95, 1998</Citation>
-<Title>The "prismane" protein resolved: X-ray structure at 1.7 angstroms and multiple spectroscopy of two novel 4Fe clusters.</Title>
-<Xref>DOI:10.1007/s007750050210</Xref>
-<Note>oxidized form; X-ray diffraction, 1.7 angstroms; EPR, Moessbauer, and MCD spectrographic analysis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Aragao, D.</Author>
-<Author>Macedo, S.</Author>
-<Author>Mitchell, E.P.</Author>
-<Author>Romao, C.V.</Author>
-<Author>Liu, M.Y.</Author>
-<Author>Frazao, C.</Author>
-<Author>Saraiva, L.M.</Author>
-<Author>Xavier, A.V.</Author>
-<Author>LeGall, J.</Author>
-<Author>van Dongen, W.M.A.M.</Author>
-<Author>Hagen, W.R.</Author>
-<Author>Teixeira, M.</Author>
-<Author>Carrondo, M.A.</Author>
-<Author>Lindley, P.</Author>
-</Authors>
-<Citation>J. Biol. Inorg. Chem. 8, 540-548, 2003</Citation>
-<Title>Reduced hybrid cluster proteins (HCP) from Desulfovibrio desulfuricans ATCC 27774 and Desulfovibrio vulgaris (Hildenborough): X-ray structures at high resolution using synchrotron radiation.</Title>
-<Xref>DOI:10.1007/s00775-003-0443-x</Xref>
-<Xref>PMID:12764602</Xref>
-<Note>X-ray diffraction, 1.25 angstroms; structure after reduction by dithionite; it is not demonstrated that the oxidized structure can be recovered after reduction by dithionite</Note>
-</ReferenceBlock>
-<Comment>The name "prismane" for this hybrid cluster is a now known to be a misnomer. The structure determined by X-ray consists of a four iron cluster with mixed ligands. One of the oxygen ligands, designated here as the mu-1:3-oxido, is actually partially occupied by an unidentified atom and is probably the reactive center.</Comment>
-<Comment>Because of the uncertainty in the structure, a formal charge cannot be calculated.</Comment>
-<SequenceCode>
-<SequenceSpec>C, C, C, C, E, E, H</SequenceSpec>
-<Condition>cross-link 7</Condition>
-<Condition>secondary to RESID:AA0269</Condition>
-<Xref>GO:0018301</Xref>
-<Xref>PSI-MOD:00273</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>4Fe-2S-3O</Keyword>
-<Keyword>iron-sulfur protein</Keyword>
-<Keyword>metalloprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="metal__iron-oxo-sulfur (4fe-2o-2s)">METAL Iron-oxo-sulfur (4Fe-2O-2S)</Feature>
-<Feature type="UniProt" key="metal__iron-oxo-sulfur (4fe-2o-2s); via tele nitrogen__h">METAL Iron-oxo-sulfur (4Fe-2O-2S); via tele nitrogen</Feature>
-<Feature type="UniProt" key="metal__iron-oxo-sulfur (4fe-2o-2s); via persulfide group__h">METAL Iron-oxo-sulfur (4Fe-2O-2S); via persulfide group</Feature>
-</Features>
-<Image src="/images/AA0268.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0268.PDB" />
-</Entry>
-<Entry id="AA0269">
-<Header>
-<Code>AA0269</Code>
-<Dates>
-<CreationDate>14-May-1999</CreationDate>
-<StrucRevDate>14-May-1999</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-cysteine persulfide</Name>
-<AlternateName>2-amino-3-disulfanylpropanoic acid</AlternateName>
-<AlternateName>2-amino-3-hydrodisulfidopropanoic acid</AlternateName>
-<AlternateName>2-amino-3-hydropersulfidopropanoic acid</AlternateName>
-<AlternateName>2-amino-3-persulfhydrylpropanoic acid</AlternateName>
-<AlternateName>3-(thiosulfeno)-alanine</AlternateName>
-<AlternateName>3-disulfanylalanine</AlternateName>
-<AlternateName>S-mercaptocysteine</AlternateName>
-<AlternateName>S-sulfanylcysteine</AlternateName>
-<AlternateName>thiocysteine</AlternateName>
-<SystematicName>(R)-2-amino-3-disulfanylpropanoic acid</SystematicName>
-<Xref>CAS:5652-32-4</Xref>
-<Xref>ChEBI:61963</Xref>
-<Xref>PDBHET:CSS</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 5 N 1 O 1 S 2</Formula>
-<Weight type="chemical">135.20</Weight>
-<Weight type="physical">134.981256</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 0 H 0 N 0 O 0 S 1</Formula>
-<Weight type="chemical">32.06</Weight>
-<Weight type="physical">31.972071</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Branzoli, U.</Author>
-<Author>Massey, V.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 249, 4346-4349, 1974</Citation>
-<Title>Evidence for an active site persulfide residue in rabbit liver aldehyde oxidase.</Title>
-<Xref>PMID:4276457</Xref>
-<Note>investigation of persulfide group chemistry</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Zheng, L.</Author>
-<Author>White, R.H.</Author>
-<Author>Cash, V.L.</Author>
-<Author>Dean, D.R.</Author>
-</Authors>
-<Citation>Biochemistry 33, 4714-4720, 1994</Citation>
-<Title>Mechanism for the desulfurization of L-cysteine catalyzed by the nifS gene product.</Title>
-<Xref>DOI:10.1021/bi00181a031</Xref>
-<Xref>PMID:8161529</Xref>
-<Note>chemical detection of persulfide group</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Arendsen, A.F.</Author>
-<Author>Hadden, J.</Author>
-<Author>Card, G.</Author>
-<Author>McAlpine, A.S.</Author>
-<Author>Bailey, S.</Author>
-<Author>Zaitsev, V.</Author>
-<Author>Duke, E.H.M.</Author>
-<Author>Lindley, P.F.</Author>
-<Author>Kroeckel, M.</Author>
-<Author>Trautwein, A.X.</Author>
-<Author>Feiters, M.C.</Author>
-<Author>Charnock, J.M.</Author>
-<Author>Garner, C.D.</Author>
-<Author>Marritt, S.J.</Author>
-<Author>Thomson, A.J.</Author>
-<Author>Kooter, I.M.</Author>
-<Author>Johnson, M.K.</Author>
-<Author>van den Berg, W.A.M.</Author>
-<Author>van Dongen, W.M.A.M.</Author>
-<Author>Hagen, W.R.</Author>
-</Authors>
-<Citation>J. Biol. Inorg. Chem. 3, 81-95, 1998</Citation>
-<Title>The "prismane" protein resolved: X-ray structure at 1.7 angstroms and multiple spectroscopy of two novel 4Fe clusters.</Title>
-<Xref>DOI:10.1007/s007750050210</Xref>
-<Note>X-ray diffraction, 1.7 angstroms; EPR, Moessbauer, and MCD spectrographic analysis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>de Beus, M.D.</Author>
-<Author>Chung, J.</Author>
-<Author>Colon, W.</Author>
-</Authors>
-<Citation>Protein Sci. 13, 1347-1355, 2004</Citation>
-<Title>Modification of cysteine 111 in Cu/Zn superoxide dismutase results in altered spectroscopic and biophysical properties.</Title>
-<Xref>DOI:10.1110/ps.03576904</Xref>
-<Xref>PMID:15096637</Xref>
-<Note>spectrographic, and mass spectrometric detection; chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Urich, T.</Author>
-<Author>Gomes, C.M.</Author>
-<Author>Kletzin, A.</Author>
-<Author>Frazão, C.</Author>
-</Authors>
-<Citation>Science 311, 996-1000, 2006</Citation>
-<Title>X-ray Structure of a self-compartmentalizing sulfur cycle metalloenzyme.</Title>
-<Xref>DOI:10.1126/science.1120306</Xref>
-<Xref>PMID:16484493</Xref>
-<Note>X-ray diffraction, 1.70 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Urich, T.</Author>
-<Author>Gomes, C.M.</Author>
-<Author>Kletzin, A.</Author>
-<Author>Frazao, C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, December 2005</Citation>
-<Description>Sulfur oxygenase reductase from Acidianus ambivalens.</Description>
-<Xref>PDB:2CB2</Xref>
-<Note>X-ray diffraction, 1.70 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mustafa, A.K.</Author>
-<Author>Gadalla, M.M.</Author>
-<Author>Sen, N.</Author>
-<Author>Kim, S.</Author>
-<Author>Mu, W.</Author>
-<Author>Gazi, S.K.</Author>
-<Author>Barrow, R.K.</Author>
-<Author>Yang, G.</Author>
-<Author>Wang, R.</Author>
-<Author>Snyder, S.H.</Author>
-</Authors>
-<Citation>Science Signal. 2, ra72, 2009</Citation>
-<Title>H2S signals through protein S-sulfhydration.</Title>
-<Xref>DOI:10.1126/scisignal.2000464</Xref>
-<Xref>PMID:19903941</Xref>
-</ReferenceBlock>
-<Comment>In desulfurization, the sulfur is donated by free cysteine to peptidyl-cysteine producing free alanine and peptidyl-cysteine persulfide. See also RESID:AA0101 and RESID:AA0268.</Comment>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>GO:0018179</Xref>
-<Xref>GO:0018192</Xref>
-<Xref>PSI-MOD:00274</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="act_site____c">ACT_SITE</Feature>
-<Feature type="UniProt" key="act_site__cysteine persulfide intermediate__c">ACT_SITE Cysteine persulfide intermediate</Feature>
-<Feature type="UniProt" key="mod_res__cysteine persulfide__c">MOD_RES Cysteine persulfide</Feature>
-</Features>
-<Image src="/images/AA0269.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0269.PDB" />
-</Entry>
-<Entry id="AA0270">
-<Header>
-<Code>AA0270</Code>
-<Dates>
-<CreationDate>14-May-1999</CreationDate>
-<StrucRevDate>14-May-1999</StrucRevDate>
-<TextChngDate>31-Dec-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>3'-(1'-L-histidyl)-L-tyrosine</Name>
-<AlternateName>3'-(N(epsilon)-histidyl)tyrosine</AlternateName>
-<AlternateName>3'-(N1'-histidyl)tyrosine</AlternateName>
-<AlternateName>3'-(tau-histidyl)tyrosine</AlternateName>
-<AlternateName>3'-(tele-histidyl)tyrosine</AlternateName>
-<SystematicName>(2S)-2-amino-3-[1-(5-[(2S)-2-amino-2-carboxyethyl]-2-hydroxyphenyl)-1H-imidazol-4-yl]propanoic acid</SystematicName>
-<Xref>ChEBI:19837</Xref>
-<Xref>COMe:BIM000381</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 15 H 14 N 4 O 3</Formula>
-<Weight type="chemical">298.30</Weight>
-<Weight type="physical">298.106590</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0009 AA0019">
-<Formula>C 0 H -2 N 0 O 0</Formula>
-<Weight type="chemical">-2.02</Weight>
-<Weight type="physical">-2.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Buse, G.</Author>
-<Author>Soulimane, T.</Author>
-<Author>Dewor, M.</Author>
-<Author>Meyer, H.E.</Author>
-<Author>Blueggel, M.</Author>
-</Authors>
-<Citation>Protein Sci. 8, 985-990, 1999</Citation>
-<Title>Evidence for a copper-coordinated histidine-tyrosine cross-link in the active site of cytochrome oxidase.</Title>
-<Xref>DOI:10.1110/ps.8.5.985</Xref>
-<Xref>PMID:10338009</Xref>
-<Note>mass spectrometric and chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hemp, J.</Author>
-<Author>Robinson, D.E.</Author>
-<Author>Ganesan, K.B.</Author>
-<Author>Martinez, T.J.</Author>
-<Author>Kelleher, N.L.</Author>
-<Author>Gennis, R.B.</Author>
-</Authors>
-<Citation>Biochemistry 45, 15405-15410, 2006</Citation>
-<Title>Evolutionary migration of a post-translationally modified active-site residue in the proton-pumping heme-copper oxygen reductases.</Title>
-<Xref>DOI:10.1021/bi062026u</Xref>
-<Xref>PMID:17176062</Xref>
-<Note>mass spectrometric detection</Note>
-</ReferenceBlock>
-<Comment>This modification is different from the modification 3-(3'-L-histidyl)-L-tyrosine, see RESID:AA0250.</Comment>
-<SequenceCode>
-<SequenceSpec>H, Y</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>GO:0018152</Xref>
-<Xref>PSI-MOD:00275</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="crosslnk__1&apos;-histidyl-3&apos;-tyrosine (his-tyr)__h__y">CROSSLNK 1'-histidyl-3'-tyrosine (His-Tyr)</Feature>
-</Features>
-<Image src="/images/AA0270.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0270.PDB" />
-</Entry>
-<Entry id="AA0271">
-<Header>
-<Code>AA0271</Code>
-<Dates>
-<CreationDate>30-Sep-1999</CreationDate>
-<StrucRevDate>31-Dec-2009</StrucRevDate>
-<TextChngDate>31-Dec-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>heme P460-bis-L-cysteine-L-lysine</Name>
-<AlternateName>bis(S-cysteinyl)-N6-lysino-heme</AlternateName>
-<SystematicName>(19S,20S)-[7,12-bis((S)-1-[((R)-2-amino-2-carboxy)ethylsulfanyl]ethyl)-20-([(S)-5-amino-5-carboxypentyl]amino)-3,8,13,17-tetramethyl-21H,23H-19,20-dihydroporphine-2,18-bis(2-carboxyethyl)-N21,N22,N23,N24]-ferrate</SystematicName>
-<Xref>PDBHET:HEC</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 46 Fe 1 H 54 N 8 O 7 S 2</Formula>
-<Weight type="chemical">950.95</Weight>
-<Weight type="physical">950.290626</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005 AA0012">
-<Formula>C 34 Fe 1 H 32 N 4 O 4 S 0</Formula>
-<Weight type="chemical">616.50</Weight>
-<Weight type="physical">616.177293</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Arciero, D.M.</Author>
-<Author>Hooper, A.B.</Author>
-</Authors>
-<Citation>FEBS Lett. 410, 457-460, 1997</Citation>
-<Title>Evidence for a crosslink between c-heme and a lysine residue in cytochrome P460 of Nitrosomonas europaea.</Title>
-<Xref>DOI:10.1016/S0014-5793(97)00635-2</Xref>
-<Xref>PMID:9237682</Xref>
-<Note>spectrographic characterization; chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bergmann, D.J.</Author>
-<Author>Hooper, A.B.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 270, 1935-1941, 2003</Citation>
-<Title>Cytochrome P460 of Nitrosomonas europaea. Formation of the heme-lysine cross-link in a heterologous host and mutagenic conversion to a non-cross-linked cytochrome c'.</Title>
-<Xref>DOI:10.1046/j.1432-1033.2003.03550.x</Xref>
-<Xref>PMID:12709052</Xref>
-<Note>mutagenic analysis; catalytic characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Pearson, A.R.</Author>
-<Author>Elmore, B.O.</Author>
-<Author>Yang, C.</Author>
-<Author>Ferrara, J.D.</Author>
-<Author>Hooper, A.B.</Author>
-<Author>Wilmot, C.M.</Author>
-</Authors>
-<Citation>Biochemistry 46, 8340-8349, 2007</Citation>
-<Title>The crystal structure of cytochrome P460 of Nitrosomonas europaea reveals a novel cytochrome fold and heme-protein cross-link.</Title>
-<Xref>DOI:10.1021/bi700086r</Xref>
-<Xref>PMID:17583915</Xref>
-<Note>X-ray diffraction, 1.8 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Pearson, A.R.</Author>
-<Author>Elmore, B.O.</Author>
-<Author>Yang, C.</Author>
-<Author>Ferrara, J.D.</Author>
-<Author>Hooper, A.B.</Author>
-<Author>Wilmot, C.M.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, January 2007</Citation>
-<Description>Cytochrome P460 from Nitrosomonas europaea - probable physiological form.</Description>
-<Xref>PDB:2JE3</Xref>
-<Note>X-ray diffraction, 1.8 angstroms</Note>
-</ReferenceBlock>
-<Comment>The heme-lysine cross-link is probably produced auto-catalytically. See RESID:AA0266.</Comment>
-<SequenceCode>
-<SequenceSpec>C, C, K</SequenceSpec>
-<Condition>cross-link 3</Condition>
-<Xref>GO:0018174</Xref>
-<Xref>GO:0018360</Xref>
-<Xref>PSI-MOD:00276</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chromoprotein</Keyword>
-<Keyword>heme</Keyword>
-<Keyword>iron</Keyword>
-<Keyword>metalloprotein</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="binding__heme (covalent; via 3 links)__k">BINDING Heme (covalent; via 3 links)</Feature>
-</Features>
-<Image src="/images/AA0271.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0271.PDB" />
-</Entry>
-<Entry id="AA0272">
-<Header>
-<Code>AA0272</Code>
-<Dates>
-<CreationDate>30-Sep-1999</CreationDate>
-<StrucRevDate>30-Sep-1999</StrucRevDate>
-<TextChngDate>30-Sep-2008</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>5-methyl-L-arginine</Name>
-<AlternateName>2-amino-5-guanidinohexanoic acid</AlternateName>
-<AlternateName>4-methylarginine [misnomer]</AlternateName>
-<AlternateName>delta-methylarginine</AlternateName>
-<SystematicName>(2S,5S)-2-amino-5-carbamimidamidohexanoic acid</SystematicName>
-<Xref>PDBHET:AGM</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 14 N 4 O 1</Formula>
-<Weight type="chemical">170.22</Weight>
-<Weight type="physical">170.116761</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0002">
-<Formula>C 1 H 2 N 0 O 0</Formula>
-<Weight type="chemical">14.03</Weight>
-<Weight type="physical">14.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ermler, U.</Author>
-<Author>Grabarse, W.</Author>
-<Author>Shima, S.</Author>
-<Author>Goubeaud, M.</Author>
-<Author>Thauer, R.K.</Author>
-</Authors>
-<Citation>Science 278, 1457-1462, 1997</Citation>
-<Title>Crystal structure of methyl-coenzyme M reductase: the key enzyme of biological methane formation.</Title>
-<Xref>DOI:10.1126/science.278.5342.1457</Xref>
-<Xref>PMID:9367957</Xref>
-<Note>X-ray diffraction, 1.45 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Selmer, T.</Author>
-<Author>Kahnt, J.</Author>
-<Author>Goubeaud, M.</Author>
-<Author>Shima, S.</Author>
-<Author>Grabarse, W.</Author>
-<Author>Ermler, U.</Author>
-<Author>Thauer, R.K.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 275, 3755-3760, 2000</Citation>
-<Title>The biosynthesis of methylated amino acids in the active site region of methyl-coenzyme M reductase.</Title>
-<Xref>DOI:10.1074/jbc.275.6.3755</Xref>
-<Xref>PMID:10660523</Xref>
-<Note>mass spectrometric characterization; the biosynthetic origin of the methyl group is S-adenosyl methionine, not methyl-coenzyme M</Note>
-</ReferenceBlock>
-<Comment>This modification should not be confused with N5-methylarginine (see RESID:AA0305).</Comment>
-<Comment>In methyl-coenzyme M reductase the arginine 5-methyl group is derived from S-adenosyl-methionine and is not produced as a side reaction of the enzyme.</Comment>
-<SequenceCode>
-<SequenceSpec>R</SequenceSpec>
-<Xref>GO:0018181</Xref>
-<Xref>PSI-MOD:00277</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>methylated amino acid</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__5-methylarginine__r">MOD_RES 5-methylarginine</Feature>
-</Features>
-<Image src="/images/AA0272.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0272.PDB" />
-</Entry>
-<Entry id="AA0273">
-<Header>
-<Code>AA0273</Code>
-<Dates>
-<CreationDate>30-Sep-1999</CreationDate>
-<StrucRevDate>30-Sep-1999</StrucRevDate>
-<TextChngDate>30-Sep-2008</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>2-methyl-L-glutamine</Name>
-<AlternateName>2-methylglutamine</AlternateName>
-<AlternateName>alpha-methylglutamine</AlternateName>
-<SystematicName>(S)-2-amino-2-methylpentanediamic acid</SystematicName>
-<Xref>CAS:4247-16-9</Xref>
-<Xref>PDBHET:MGN</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 10 N 2 O 2</Formula>
-<Weight type="chemical">142.16</Weight>
-<Weight type="physical">142.074228</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0007">
-<Formula>C 1 H 2 N 0 O 0</Formula>
-<Weight type="chemical">14.03</Weight>
-<Weight type="physical">14.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ermler, U.</Author>
-<Author>Grabarse, W.</Author>
-<Author>Shima, S.</Author>
-<Author>Goubeaud, M.</Author>
-<Author>Thauer, R.K.</Author>
-</Authors>
-<Citation>Science 278, 1457-1462, 1997</Citation>
-<Title>Crystal structure of methyl-coenzyme M reductase: the key enzyme of biological methane formation.</Title>
-<Xref>DOI:10.1126/science.278.5342.1457</Xref>
-<Xref>PMID:9367957</Xref>
-<Note>X-ray diffraction, 1.45 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Selmer, T.</Author>
-<Author>Kahnt, J.</Author>
-<Author>Goubeaud, M.</Author>
-<Author>Shima, S.</Author>
-<Author>Grabarse, W.</Author>
-<Author>Ermler, U.</Author>
-<Author>Thauer, R.K.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 275, 3755-3760, 2000</Citation>
-<Title>The biosynthesis of methylated amino acids in the active site region of methyl-coenzyme M reductase.</Title>
-<Xref>DOI:10.1074/jbc.275.6.3755</Xref>
-<Xref>PMID:10660523</Xref>
-<Note>mass spectrometric characterization; the biosynthetic origin of the methyl group is S-adenosyl methionine, not methyl-coenzyme M</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>Q</SequenceSpec>
-<Xref>GO:0018361</Xref>
-<Xref>PSI-MOD:00278</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>methylated amino acid</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__2-methylglutamine__q">MOD_RES 2-methylglutamine</Feature>
-</Features>
-<Image src="/images/AA0273.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0273.PDB" />
-</Entry>
-<Entry id="AA0274">
-<Header>
-<Code>AA0274</Code>
-<Dates>
-<CreationDate>30-Sep-1999</CreationDate>
-<StrucRevDate>30-Sep-1999</StrucRevDate>
-<TextChngDate>30-Sep-2008</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-pyruvic acid 2-iminyl-L-cysteine</Name>
-<SystematicName>(R)-2-(1-carboxy-2-sulfanylethanimino)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 8 N 1 O 3 S 1</Formula>
-<Weight type="chemical">174.19</Weight>
-<Weight type="physical">174.022489</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 3 H 2 N 0 O 2 S 0</Formula>
-<Weight type="chemical">70.05</Weight>
-<Weight type="physical">70.005479</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Rose, K.</Author>
-<Author>Simona, M.G.</Author>
-<Author>Savoy, L.A.</Author>
-<Author>Regamey, P.O.</Author>
-<Author>Green, B.N.</Author>
-<Author>Clore, G.M.</Author>
-<Author>Gronenborn, A.M.</Author>
-<Author>Wingfield, P.T.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 267, 19101-19106, 1992</Citation>
-<Title>Pyruvic acid is attached through its central carbon atom to the amino terminus of the recombinant DNA-derived DNA-binding protein Ner of bacteriophage Mu.</Title>
-<Xref>PMID:1388164</Xref>
-<Note>mass spectrometric and chemical characterization; (1)H-NMR identification; 2,4-dinitrophenylhydrazine used for detection</Note>
-</ReferenceBlock>
-<Comment>The cysteine sulfhydryl may cyclize with the imine to form 2-methyl-thiazolidine-2,4-dicarboxylic acid [CAS:152574-58-8].</Comment>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0018386</Xref>
-<Xref>PSI-MOD:00279</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n-pyruvate 2-iminyl-cysteine__c">MOD_RES N-pyruvate 2-iminyl-cysteine</Feature>
-</Features>
-<Image src="/images/AA0274.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0274.PDB" />
-</Entry>
-<Entry id="AA0275">
-<Header>
-<Code>AA0275</Code>
-<Dates>
-<CreationDate>30-Sep-1999</CreationDate>
-<StrucRevDate>30-Sep-1999</StrucRevDate>
-<TextChngDate>30-Sep-2008</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-pyruvic acid 2-iminyl-L-valine</Name>
-<SystematicName>(S)-2-(1-carboxy-2-methylpropanimino)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 8 H 12 N 1 O 3</Formula>
-<Weight type="chemical">170.19</Weight>
-<Weight type="physical">170.081718</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0020">
-<Formula>C 3 H 2 N 0 O 2</Formula>
-<Weight type="chemical">70.05</Weight>
-<Weight type="physical">70.005479</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Prome, D.</Author>
-<Author>Blouquit, Y.</Author>
-<Author>Ponthus, C.</Author>
-<Author>Prome, J.C.</Author>
-<Author>Rosa, J.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 266, 13050-13054, 1991</Citation>
-<Title>Structure of the human adult hemoglobin minor fraction A-1b by electrospray and secondary ion mass spectrometry. Pyruvic acid as amino-terminal blocking group.</Title>
-<Xref>PMID:2071591</Xref>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>V</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0018388</Xref>
-<Xref>PSI-MOD:00280</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n-pyruvate 2-iminyl-valine__v">MOD_RES N-pyruvate 2-iminyl-valine</Feature>
-</Features>
-<Image src="/images/AA0275.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0275.PDB" />
-</Entry>
-<Entry id="AA0276">
-<Header>
-<Code>AA0276</Code>
-<Dates>
-<CreationDate>30-Sep-1999</CreationDate>
-<StrucRevDate>31-Dec-2002</StrucRevDate>
-<TextChngDate>13-Sep-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>3'-heme-L-histidine</Name>
-<AlternateName>2-[1-(N3'-histidyl)ethyl]protoporphyrin IX</AlternateName>
-<AlternateName>N(delta)-histidyl heme</AlternateName>
-<AlternateName>N(pi)-histidyl heme</AlternateName>
-<AlternateName>N3'-histidyl heme</AlternateName>
-<AlternateName>pros-histidyl heme</AlternateName>
-<SystematicName>[7-ethenyl-12-((S)-1-[((R)-2-amino-2-carboxyethyl)-3H-imidazol-3-yl]ethyl)-3,8,13,17-tetramethyl-21H,23H-porphine-2,18-bis(2-carboxyethyl)-N21,N22,N23,N24]-ferrate</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 40 Fe 1 H 39 N 7 O 5</Formula>
-<Weight type="chemical">753.64</Weight>
-<Weight type="physical">753.236205</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0009">
-<Formula>C 34 Fe 1 H 32 N 4 O 4</Formula>
-<Weight type="chemical">616.50</Weight>
-<Weight type="physical">616.177293</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Schulz, H.</Author>
-<Author>Hennecke, H.</Author>
-<Author>Thoeny-Meyer, L.</Author>
-</Authors>
-<Citation>Science 281, 1197-1200, 1998</Citation>
-<Title>Prototype of a heme chaperone essential for cytochrome c maturation.</Title>
-<Xref>DOI:10.1126/science.281.5380.1197</Xref>
-<Xref>PMID:9712585</Xref>
-<Note>mass spectrometric identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Daltrop, O.</Author>
-<Author>Stevens, J.M.</Author>
-<Author>Higham, C.W.</Author>
-<Author>Ferguson, S.J.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 99, 9703-9708, 2002</Citation>
-<Title>The CcmE protein of the c-type cytochrome biogenesis system: Unusual in vitro heme incorporation into apo-CcmE and transfer from holo-CcmE to apocytochrome.</Title>
-<Xref>DOI:10.1073/pnas.152120699</Xref>
-<Xref>PMID:12119398</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Enggist, E.</Author>
-<Author>Thoeny-Meyer, L.</Author>
-<Author>Guentert, P.</Author>
-<Author>Pervushin, K.</Author>
-</Authors>
-<Citation>Structure 10, 1551-1557, 2002</Citation>
-<Title>NMR structure of the heme chaperone CcmE reveals a novel functional motif.</Title>
-<Xref>DOI:10.1016/S0969-2126(02)00885-7</Xref>
-<Xref>PMID:12429096</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Enggist, E.</Author>
-<Author>Schneider, M.J.</Author>
-<Author>Schulz, H.</Author>
-<Author>Thoeny-Meyer, L.</Author>
-</Authors>
-<Citation>J. Bacteriol. 185, 175-183, 2003</Citation>
-<Title>Biochemical and mutational characterization of the heme chaperone CcmE reveals a heme binding site.</Title>
-<Xref>DOI:10.1128/JB.185.1.175-183.2003</Xref>
-<Xref>PMID:12486054</Xref>
-<Note>directed mutation analysis; spectrographic characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Enggist, E.</Author>
-<Author>Thony-Meyer, L.</Author>
-<Author>Guntert, P.</Author>
-<Author>Pervushin, K.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, March 2004</Citation>
-<Description>Solution structure of the heme chaperone CcmE of Escherichia coli.</Description>
-<Xref>PDB:1SR3</Xref>
-<Note>conformation by NMR; these models do not include the heme</Note>
-</ReferenceBlock>
-<Comment>The NMR model structure and the spectrographic characterization suggest, but do not establish, that the heme is attached to the pros-nitrogen.</Comment>
-<SequenceCode>
-<SequenceSpec>H</SequenceSpec>
-<Xref>GO:0018182</Xref>
-<Xref>PSI-MOD:00281</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chromoprotein</Keyword>
-<Keyword>heme</Keyword>
-<Keyword>iron</Keyword>
-<Keyword>metalloprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="binding__heme (covalent; via pros nitrogen)__h">BINDING Heme (covalent; via pros nitrogen)</Feature>
-</Features>
-<Image src="/images/AA0276.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0276.PDB" />
-</Entry>
-<Entry id="AA0277">
-<Header>
-<Code>AA0277</Code>
-<Dates>
-<CreationDate>24-Nov-1999</CreationDate>
-<StrucRevDate>24-Nov-1999</StrucRevDate>
-<TextChngDate>24-Aug-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-selanyl-L-cysteine</Name>
-<AlternateName>2-amino-3-hydroselenosulfidopropanoic acid</AlternateName>
-<AlternateName>2-amino-3-hydroselenylsulfidopropanoic acid</AlternateName>
-<AlternateName>2-amino-3-hydroselenylthiopropanoic acid</AlternateName>
-<AlternateName>cysteine perselenide [misnomer]</AlternateName>
-<AlternateName>S-selanylcysteine</AlternateName>
-<AlternateName>S-selenylcysteine</AlternateName>
-<SystematicName>(R)-2-amino-3-(selanylsulfanyl)propanoic acid</SystematicName>
-<Xref>PDBHET:CSZ</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 5 N 1 O 1 S 1 Se 1</Formula>
-<Weight type="chemical">182.11</Weight>
-<Weight type="physical">182.925706</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 0 H 0 N 0 O 0 S 0 Se 1</Formula>
-<Weight type="chemical">78.97</Weight>
-<Weight type="physical">79.916521</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Dobbek, H.</Author>
-<Author>Gremer, L.</Author>
-<Author>Meyer, O.</Author>
-<Author>Huber, R.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 96, 8884-8889, 1999</Citation>
-<Title>Crystal structure and mechanism of CO dehydrogenase, a molybdo iron-sulfur flavoprotein containing S-selanylcysteine.</Title>
-<Xref>DOI:10.1073/pnas.96.16.8884</Xref>
-<Xref>PMID:10430865</Xref>
-<Note>X-ray diffraction, 2.2 angstroms; this structure has been revised with a metal cluster that does not contain selenium, see RESID:AA0355</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Haenzelmann, P.</Author>
-<Author>Dobbek, H.</Author>
-<Author>Gremer, L.</Author>
-<Author>Huber, R.</Author>
-<Author>Meyer, O.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 301, 1221-1235, 2000</Citation>
-<Title>The effect of intracellular molybdenum in Hydrogenophaga pseudoflava on the crystallographic structure of the seleno-molybdo-iron-sulfur flavoenzyme carbon monoxide dehydrogenase.</Title>
-<Xref>DOI:10.1006/jmbi.2000.4023</Xref>
-<Xref>PMID:10966817</Xref>
-<Note>X-ray diffraction, 2.25 angstroms; this structure may not be correct, see RESID:AA0355</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Haenzelmann, P.</Author>
-<Author>Dobbek, H.</Author>
-<Author>Gremer, L.</Author>
-<Author>Huber, R.</Author>
-<Author>Meyer, O.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, September 2000</Citation>
-<Description>Carbon monoxide dehydrogenase from Hydrogenophaga pseudoflava.</Description>
-<Xref>PDB:1FFV</Xref>
-<Note>X-ray diffraction, 2.25 angstroms; this structure may not be correct, see RESID:AA0355</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lima, C.D.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 315, 1199-1208, 2002</Citation>
-<Title>Analysis of the E. coli NifS CsdB protein at 2.0 A reveals the structural basis for perselenide and persulfide intermediate formation.</Title>
-<Xref>DOI:10.1006/jmbi.2001.5308</Xref>
-<Xref>PMID:11827487</Xref>
-<Note>X-ray diffraction, 2.2 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lima, C.D.</Author>
-<Author>Burley, S.K.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, December 2001</Citation>
-<Description>E. coli NifS/CsdB protein at 2.20 A with the cysteine perselenide intermediate (residue CSZ).</Description>
-<Xref>PDB:1KMK</Xref>
-<Note>X-ray diffraction, 2.20 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wolfe, M.D.</Author>
-<Author>Ahmed, F.</Author>
-<Author>Lacourciere, G.M.</Author>
-<Author>Lauhon, C.T.</Author>
-<Author>Stadtman, T.C.</Author>
-<Author>Larson, T.J.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 279, 1801-1809, 2004</Citation>
-<Title>Functional diversity of the rhodanese homology domain: the Escherichia coli ybbB gene encodes a selenophosphate-dependent tRNA 2-selenouridine synthase.</Title>
-<Xref>DOI:10.1074/jbc.M310442200</Xref>
-<Xref>PMID:14594807</Xref>
-<Note>evidence for a potential active site S-selanylcysteine intermediate in 2-selenouridine synthetase</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>GO:0018183</Xref>
-<Xref>PSI-MOD:00282</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>selenium</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="act_site__s-selanylcysteine intermediate__c">ACT_SITE S-selanylcysteine intermediate</Feature>
-<Feature type="UniProt" key="mod_res__s-selanylcysteine__c">MOD_RES S-selanylcysteine</Feature>
-</Features>
-<Image src="/images/AA0277.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0277.PDB" />
-</Entry>
-<Entry id="AA0278">
-<Header>
-<Code>AA0278</Code>
-<Dates>
-<CreationDate>24-Nov-1999</CreationDate>
-<StrucRevDate>06-Feb-2004</StrucRevDate>
-<TextChngDate>30-Jun-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6-propylamino-poly(propylmethylamino)-propyldimethylamine-L-lysine</Name>
-<AlternateName>lysine derivative Lys(x)</AlternateName>
-<AlternateName>N6-[3-([(omega)-(dimethyl)aminopropyl-poly(3-[methylamino]propyl)]amino)propyl]lysine</AlternateName>
-<AlternateName>silaffin polycationic lysine derivative</AlternateName>
-<SystematicName>(alpha)- ([([(5S)-5-amino-5-carboxypentyl]amino)propyl][(methyl)amino])-(omega)-methyl poly[propane-1,3-diyl(methylimino)]</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 30 H 66 N 8 O 1 +</Formula>
-<Weight type="chemical">554.91 +</Weight>
-<Weight type="physical">554.535959 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 24 H 54 N 6 O 0 +</Formula>
-<Weight type="chemical">426.74 +</Weight>
-<Weight type="physical">426.440996 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kroeger, N.</Author>
-<Author>Deutzmann, R.</Author>
-<Author>Sumper, M.</Author>
-</Authors>
-<Citation>Science 286, 1129-1132, 1999</Citation>
-<Title>Polycationic peptides from diatom biosilica that direct silica nanosphere formation.</Title>
-<Xref>DOI:10.1126/science.286.5442.1129</Xref>
-<Xref>PMID:10550045</Xref>
-<Note>chromatographic, mass spectrometric and (1)H-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kroeger, N.</Author>
-<Author>Deutzmann, R.</Author>
-<Author>Sumper, M.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 276, 26066-26070, 2001</Citation>
-<Title>Silica-precipitating peptides from diatoms. The chemical structure of silaffin-A from Cylindrotheca fusiformis.</Title>
-<Xref>DOI:10.1074/jbc.M102093200</Xref>
-<Xref>PMID:11349130</Xref>
-<Note>chromatographic and mass spectrometric identification</Note>
-</ReferenceBlock>
-<Comment>In silaffin from the diatom Cylindrotheca fusiformis there are five to eleven N-methyl-propylamine monomeric units on each lysine. Six are shown.</Comment>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>GO:0018185</Xref>
-<Xref>PSI-MOD:00283</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>methylated amino acid</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n6-poly(methylaminopropyl)lysine__k">MOD_RES N6-poly(methylaminopropyl)lysine</Feature>
-</Features>
-<Image src="/images/AA0278.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0278.PDB" />
-</Entry>
-<Entry id="AA0279">
-<Header>
-<Code>AA0279</Code>
-<Dates>
-<CreationDate>24-Nov-1999</CreationDate>
-<StrucRevDate>24-Nov-1999</StrucRevDate>
-<TextChngDate>24-Oct-2008</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>dihydroxyheme-L-aspartate ester-L-glutamate ester</Name>
-<AlternateName>1,5-bishydroxymethyl protoporphyrin IX 1-glutamate ester 5-aspartate ester</AlternateName>
-<AlternateName>peroxidase heme cofactor</AlternateName>
-<SystematicName>[13-[(S)-(4-amino-4-carboxy)butanoyloxymethyl]-3-[(S)-(3-amino-3-carboxy)propanoyloxymethyl]-7,12-diethenyl-8,17-dimethyl-21H,23H-porphine-2,18-bis(2-carboxyethyl)-N21,N22,N23,N24]-ferrate</SystematicName>
-<Xref>COMe:BIM000243</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 43 Fe 1 H 40 N 6 O 10</Formula>
-<Weight type="chemical">856.67</Weight>
-<Weight type="physical">856.215529</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0004 AA0006">
-<Formula>C 34 Fe 1 H 28 N 4 O 4</Formula>
-<Weight type="chemical">612.47</Weight>
-<Weight type="physical">612.145993</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kooter, I.M.</Author>
-<Author>Moguilevsky, N.</Author>
-<Author>Bollen, A.</Author>
-<Author>Sijtsema, N.M.</Author>
-<Author>Otto, C.</Author>
-<Author>Dekker, H.L.</Author>
-<Author>Wever, R.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 264, 211-217, 1999</Citation>
-<Title>Characterization of the Asp94 and Glu242 mutants in myeloperoxidase, the residues linking the heme group via ester bonds.</Title>
-<Xref>DOI:10.1046/j.1432-1327.1999.00606.x</Xref>
-<Xref>PMID:10447690</Xref>
-<Note>directed mutation analysis; activity comparison</Note>
-</ReferenceBlock>
-<Comment>For structural studies of the myeloperoxidase heme cofactor, see RESID:AA0280.</Comment>
-<SequenceCode>
-<SequenceSpec>D, E</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>GO:0018186</Xref>
-<Xref>GO:0018362</Xref>
-<Xref>PSI-MOD:00284</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>chromoprotein</Keyword>
-<Keyword>heme</Keyword>
-<Keyword>hydroxylation</Keyword>
-<Keyword>iron</Keyword>
-<Keyword>metalloprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="binding__heme (covalent; via 2 links)">BINDING Heme (covalent; via 2 links)</Feature>
-</Features>
-<Image src="/images/AA0279.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0279.PDB" />
-</Entry>
-<Entry id="AA0280">
-<Header>
-<Code>AA0280</Code>
-<Dates>
-<CreationDate>24-Nov-1999</CreationDate>
-<StrucRevDate>24-Nov-1999</StrucRevDate>
-<TextChngDate>31-Dec-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>dihydroxyheme-L-aspartate ester-L-glutamate ester-L-methionine sulfonium</Name>
-<AlternateName>1,5-bishydroxymethyl protoporphyrin IX 1-glutamate ester 5-aspartate ester 2-methionine sulfonium</AlternateName>
-<AlternateName>myeloperoxidase heme cofactor</AlternateName>
-<SystematicName>[13-[(S)-(4-amino-4-carboxy)butanoyloxymethyl]-3-[(S)-(3-amino-3-carboxy)propanoyloxymethyl]-12-[(S)-(3-amino-3-carboxy)propylsulfoniumethyl]-7-ethenyl-8,17-dimethyl-21H,23H-porphine-2,18-bis(2-carboxyethyl)-N21,N22,N23,N24]-ferrate</SystematicName>
-<Xref>COMe:BIM000245</Xref>
-<Xref>PDBHET:HEM</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 48 Fe 1 H 50 N 7 O 11 S 1</Formula>
-<FormalCharge>1+</FormalCharge>
-<Weight type="chemical">988.87</Weight>
-<Weight type="physical">988.263290</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0004 AA0006 AA0013">
-<Formula>C 34 Fe 1 H 29 N 4 O 4 S 0</Formula>
-<FormalCharge>1+</FormalCharge>
-<Weight type="chemical">613.47</Weight>
-<Weight type="physical">613.153269</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kooter, I.M.</Author>
-<Author>Moguilevsky, N.</Author>
-<Author>Bollen, A.</Author>
-<Author>van der Veen, L.A.</Author>
-<Author>Otto, C.</Author>
-<Author>Dekker, H.L.</Author>
-<Author>Wever, R.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 274, 26794-26802, 1999</Citation>
-<Title>The sulfonium ion linkage in myeloperoxidase. Direct spectroscopic detection by and effect of mutation.</Title>
-<Xref>DOI:10.1074/jbc.274.38.26794</Xref>
-<Xref>PMID:10480885</Xref>
-<Note>radioisotope labeling; spectrographic characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kooter, I.M.</Author>
-<Author>Moguilevsky, N.</Author>
-<Author>Bollen, A.</Author>
-<Author>Sijtsema, N.M.</Author>
-<Author>Otto, C.</Author>
-<Author>Dekker, H.L.</Author>
-<Author>Wever, R.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 264, 211-217, 1999</Citation>
-<Title>Characterization of the Asp94 and Glu242 mutants in myeloperoxidase, the residues linking the heme group via ester bonds.</Title>
-<Xref>DOI:10.1046/j.1432-1327.1999.00606.x</Xref>
-<Xref>PMID:10447690</Xref>
-<Note>directed mutation analysis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fenna, R.E.</Author>
-<Author>Zeng, J.</Author>
-<Author>Davey, C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, June 1995</Citation>
-<Description>Crystal structure of human myeloperoxidase isoform C crystallized in space group P2(1) at pH 5.5 and 20 deg C.</Description>
-<Xref>PDB:1MHL</Xref>
-<Note>X-ray diffraction, 2.25 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fenna, R.</Author>
-<Author>Zeng, J.</Author>
-<Author>Davey, C.</Author>
-</Authors>
-<Citation>Arch. Biochem. Biophys. 316, 653-656, 1995</Citation>
-<Title>Structure of the green heme in myeloperoxidase.</Title>
-<Xref>DOI:10.1006/abbi.1995.1086</Xref>
-<Xref>PMID:7840679</Xref>
-<Note>X-ray diffraction, 2.25 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fenna, R.E.</Author>
-<Author>Zeng, J.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, April 1992</Citation>
-<Description>X-ray crystal structure of canine myeloperoxidase at 3 A resolution.</Description>
-<Xref>PDB:1MYP</Xref>
-<Note>X-ray diffraction, 3.0 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Zeng, J.</Author>
-<Author>Fenna, R.E.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 226, 185-207, 1992</Citation>
-<Title>X-ray crystal structure of canine myeloperoxidase at 3 Angstroms resolution.</Title>
-<Xref>DOI:10.1016/0022-2836(92)90133-5</Xref>
-<Xref>PMID:1320128</Xref>
-<Note>X-ray diffraction, 3.0 angstroms</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>D, E, M</SequenceSpec>
-<Condition>cross-link 3</Condition>
-<Xref>GO:0018186</Xref>
-<Xref>GO:0018363</Xref>
-<Xref>PSI-MOD:00285</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chromoprotein</Keyword>
-<Keyword>heme</Keyword>
-<Keyword>hydroxylation</Keyword>
-<Keyword>iron</Keyword>
-<Keyword>metalloprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="binding__heme (covalent; via 3 links)">BINDING Heme (covalent; via 3 links)</Feature>
-</Features>
-<Image src="/images/AA0280.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0280.PDB" />
-</Entry>
-<Entry id="AA0281">
-<Header>
-<Code>AA0281</Code>
-<Dates>
-<CreationDate>03-Dec-1999</CreationDate>
-<StrucRevDate>07-Sep-2001</StrucRevDate>
-<TextChngDate>31-Mar-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-cysteinyl molybdenum bis(molybdopterin guanine dinucleotide)</Name>
-<AlternateName>2-amino-5,6-dimercapto-7-methyl-3,7,8a,9-tetrahydro-8-oxa-1,3,9,10-tetraazaanthracen-4-one guanosine dinucleotide</AlternateName>
-<SystematicName>bis[8-amino-1a,2,4a,5,6,7,10-heptahydro-2-(trihydrogen diphosphate 5'-ester with guanosine)methyl-6-oxo-3,4-disulfanyl-pteridino[6,7-5,6]pyranoato-S3,S4]-cystein-S-yl-molybdenum</SystematicName>
-<Xref>CAS:128007-95-4</Xref>
-<Xref>PDBHET:MGD</Xref>
-<Xref>PDBHET:MO</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 43 H 52 Mo 1 N 21 O 27 P 4 S 5</Formula>
-<Weight type="chemical">1675.15</Weight>
-<Weight type="physical">1675.994960</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 40 H 47 Mo 1 N 20 O 26 P 4 S 4</Formula>
-<Weight type="chemical">1572.02</Weight>
-<Weight type="physical">1572.985775</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Arnoux, P.</Author>
-<Author>Sabaty, M.</Author>
-<Author>Alric, J.</Author>
-<Author>Frangioni, B.</Author>
-<Author>Guigliarelli, B.</Author>
-<Author>Adriano, J.M.</Author>
-<Author>Pignol, D.</Author>
-</Authors>
-<Citation>Nature Struct. Biol. 10, 928-934, 2003</Citation>
-<Title>Structural and redox plasticity in the heterodimeric periplasmic nitrate reductase.</Title>
-<Xref>DOI:10.1038/nsb994</Xref>
-<Xref>PMID:14528294</Xref>
-<Note>X-ray diffraction, 3.20 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Arnoux, P.</Author>
-<Author>Sabaty, M.</Author>
-<Author>Alric, J.</Author>
-<Author>Frangioni, B.</Author>
-<Author>Guigliarelli, B.</Author>
-<Author>Adriano, J.M.</Author>
-<Author>Pignol, D.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, May 2003</Citation>
-<Description>Crystal structure of the heterodimeric nitrate reductase from Rhodobacter sphaeroides.</Description>
-<Xref>PDB:1OGY</Xref>
-<Note>X-ray diffraction, 3.20 angstroms</Note>
-</ReferenceBlock>
-<Comment>One possible structure of a reduced form (+4H) is shown. The fully reduced form would be 1a,2,3,4,4a,5,6,7,10-nonahydro. The fully oxidized form would be 2,6,7-trihydro.</Comment>
-<Comment>This modification occurs in enzymes homologous to formate dehydrogenase in organisms where the position corresponding to selenocysteine instead encodes cysteine (see RESID:AA0248).</Comment>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>GO:0018187</Xref>
-<Xref>PSI-MOD:00286</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>metalloprotein</Keyword>
-<Keyword>molybdenum</Keyword>
-<Keyword>molybdopterin</Keyword>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0281.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0281.PDB" />
-</Entry>
-<Entry id="AA0282">
-<Header>
-<Code>AA0282</Code>
-<Dates>
-<CreationDate>28-Jan-2000</CreationDate>
-<StrucRevDate>28-Jan-2000</StrucRevDate>
-<TextChngDate>31-Mar-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>(2S,3R,4S)-3,4-dihydroxyproline</Name>
-<AlternateName>2,3-trans-3,4-cis-3,4-dihydroxy-L-proline</AlternateName>
-<AlternateName>2-alpha-3-beta-4-beta-3,4-dihydroxyproline</AlternateName>
-<AlternateName>trans-2,3-cis-3,4-dihydroxy-L-proline</AlternateName>
-<SystematicName>(2S,3R,4S)-3,4-dihydroxypyrrolidine-2-carboxylic acid</SystematicName>
-<Xref>CAS:95341-64-3</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 7 N 1 O 3</Formula>
-<Weight type="chemical">129.12</Weight>
-<Weight type="physical">129.042593</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0015">
-<Formula>C 0 H 0 N 0 O 2</Formula>
-<Weight type="chemical">32.00</Weight>
-<Weight type="physical">31.989829</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Taylor, S.W.</Author>
-<Author>Waite, J.H.</Author>
-<Author>Ross, M.M.</Author>
-<Author>Shabanowitz, J.</Author>
-<Author>Hunt, D.F.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 116, 10803-10804, 1994</Citation>
-<Title>trans-2,3-cis-3,4-Dihydroxyproline, a new naturally occurring amino acid, is the sixth residue in the tandemly repeated consensus decapeptides of an adhesive protein from Mytilus edulis.</Title>
-<Xref>DOI:10.1021/ja00102a063</Xref>
-<Note>chromatographic detection; mass spectrometric and (1)H-NMR identification</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>P</SequenceSpec>
-<Xref>GO:0018188</Xref>
-<Xref>PSI-MOD:00287</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__(3r,4s)-3,4-dihydroxyproline__p">MOD_RES (3R,4S)-3,4-dihydroxyproline</Feature>
-</Features>
-<Image src="/images/AA0282.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0282.PDB" />
-</Entry>
-<Entry id="AA0283">
-<Header>
-<Code>AA0283</Code>
-<Dates>
-<CreationDate>18-Feb-2000</CreationDate>
-<StrucRevDate>18-Feb-2000</StrucRevDate>
-<TextChngDate>30-Sep-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>pyrroloquinoline quinone</Name>
-<AlternateName>2,4,6-tricarboxylic-pyrrolo[2,3-5,6]quinoline 8,9-quinone</AlternateName>
-<AlternateName>2,7,9-tricarboxy-1H-pyrrolo(2,3-f)quinoline-4,5-dione</AlternateName>
-<AlternateName>coenzyme PQQ</AlternateName>
-<AlternateName>methoxatin</AlternateName>
-<SystematicName>4,5-dihydro-4,5-dioxo-1H-pyrrolo[2,3-5,6]quinoline-2,7,9-tricarboxylic acid</SystematicName>
-<Xref>CAS:72909-34-3</Xref>
-<Xref>ChEBI:18315</Xref>
-<Xref>PDBHET:PQQ</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 14 H 6 N 2 O 8</Formula>
-<Weight type="chemical">330.21</Weight>
-<Weight type="physical">330.012415</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0006 AA0019">
-<Formula>C 0 H -10 N 0 O 3</Formula>
-<Weight type="chemical">37.92</Weight>
-<Weight type="physical">37.906494</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Salisbury, S.A.</Author>
-<Author>Forrest, H.S.</Author>
-<Author>Cruse, W.B.</Author>
-<Author>Kennard, O.</Author>
-</Authors>
-<Citation>Nature 280, 843-844, 1979</Citation>
-<Title>A novel coenzyme from bacterial primary alcohol dehydrogenases.</Title>
-<Xref>PMID:471057</Xref>
-<Note>X-ray diffraction</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Duine, J.A.</Author>
-<Author>Frank Jzn., J.</Author>
-<Author>Verwiel, P.E.J.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 108, 187-192, 1980</Citation>
-<Title>Structure and Activity of the Prosthetic Group of Methanol Dehydrogenase.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1980.tb04711.x</Xref>
-<Note>chemical characterization; mass spectrometric and (1)H-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Goosen, N.</Author>
-<Author>Huinen, R.G.</Author>
-<Author>van de Putte, P.</Author>
-</Authors>
-<Citation>J. Bacteriol. 174, 1426-1427, 1992</Citation>
-<Title>A 24-amino-acid polypeptide is essential for the biosynthesis of the coenzyme pyrrolo-quinoline-quinone.</Title>
-<Xref>PMID:1310505</Xref>
-<Note>mutagenic evidence that specific glutamic acid and tyrosine residues of the pqqA protein were utilized</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Velterop, J.S.</Author>
-<Author>Sellink, E.</Author>
-<Author>Meulenberg, J.J.</Author>
-<Author>David, S.</Author>
-<Author>Bulder, I.</Author>
-<Author>Postma, P.W.</Author>
-</Authors>
-<Citation>J. Bacteriol. 177, 5088-5098, 1995</Citation>
-<Title>Synthesis of pyrroloquinoline quinone in vivo and in vitro and detection of an intermediate in the biosynthetic pathway.</Title>
-<Xref>PMID:7665488</Xref>
-<Note>evidence that the pqqA protein was the origin of pyrroloquinoline quinone</Note>
-</ReferenceBlock>
-<Comment>In some prokaryotes, the pqqA protein is the origin of pyrroloquinoline quinone. In other organisms the endogenous source, if there is one, has not been established.</Comment>
-<SequenceCode>
-<SequenceSpec>E, Y</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>GO:0018189</Xref>
-<Xref>PSI-MOD:00288</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>quinoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__pyrroloquinoline quinone (glu-tyr)__e__y">CROSSLNK Pyrroloquinoline quinone (Glu-Tyr)</Feature>
-</Features>
-<Image src="/images/AA0283.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0283.PDB" />
-</Entry>
-<Entry id="AA0284">
-<Header>
-<Code>AA0284</Code>
-<Dates>
-<CreationDate>17-Mar-2000</CreationDate>
-<StrucRevDate>17-Mar-2000</StrucRevDate>
-<TextChngDate>25-Feb-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>tris-L-cysteinyl L-N1'-histidino tetrairon tetrasulfide</Name>
-<SystematicName>tetra-mu3-sulfidotris(S-cysteinyliron)(N1'-histidinoiron)</SystematicName>
-<Xref>COMe:BIM000059</Xref>
-<Xref>PDBHET:SF4</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 15 Fe 4 H 18 N 6 O 4 S 7</Formula>
-<FormalCharge>2-</FormalCharge>
-<Weight type="chemical">794.15</Weight>
-<Weight type="physical">793.684297</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005 AA0005 AA0009">
-<Formula>C 0 Fe 4 H -4 N 0 O 0 S 4</Formula>
-<FormalCharge>2-</FormalCharge>
-<Weight type="chemical">347.59</Weight>
-<Weight type="physical">347.597831</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Peters, J.W.</Author>
-<Author>Lanzilotta, W.N.</Author>
-<Author>Lemon, B.J.</Author>
-<Author>Seefeldt, L.C.</Author>
-</Authors>
-<Citation>Science 282, 1853-1858, 1998</Citation>
-<Title>X-ray crystal structure of the Fe-only hydrogenase (CpI) from Clostridium pasteurianum to 1.8 angstrom resolution.</Title>
-<Xref>DOI:10.1126/science.282.5395.1853</Xref>
-<Xref>PMID:9836629</Xref>
-<Note>X-ray diffraction, 1.8 angstroms</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>C, C, C, H</SequenceSpec>
-<Condition>cross-link 4</Condition>
-<Xref>GO:0018302</Xref>
-<Xref>PSI-MOD:00289</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>4Fe-4S</Keyword>
-<Keyword>iron-sulfur protein</Keyword>
-<Keyword>metalloprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="metal__iron-sulfur (4fe-4s)__c">METAL Iron-sulfur (4Fe-4S)</Feature>
-<Feature type="UniProt" key="metal__iron-sulfur (4fe-4s); via tele nitrogen__h">METAL Iron-sulfur (4Fe-4S); via tele nitrogen</Feature>
-</Features>
-<Image src="/images/AA0284.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0284.PDB" />
-</Entry>
-<Entry id="AA0285">
-<Header>
-<Code>AA0285</Code>
-<Dates>
-<CreationDate>17-Mar-2000</CreationDate>
-<StrucRevDate>17-Mar-2000</StrucRevDate>
-<TextChngDate>25-Feb-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>tris-L-cysteinyl L-N3'-histidino tetrairon tetrasulfide</Name>
-<SystematicName>tetra-mu3-sulfidotris(S-cysteinyliron)(N3'-histidinoiron)</SystematicName>
-<Xref>COMe:BIM000060</Xref>
-<Xref>PDBHET:SF4</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 15 Fe 4 H 18 N 6 O 4 S 7</Formula>
-<FormalCharge>2-</FormalCharge>
-<Weight type="chemical">794.15</Weight>
-<Weight type="physical">793.684297</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005 AA0005 AA0009">
-<Formula>C 0 Fe 4 H -4 N 0 O 0 S 4</Formula>
-<FormalCharge>2-</FormalCharge>
-<Weight type="chemical">347.59</Weight>
-<Weight type="physical">347.597831</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Volbeda, A.</Author>
-<Author>Charon, M.H.</Author>
-<Author>Piras, C.</Author>
-<Author>Hatchikian, E.C.</Author>
-<Author>Frey, M.</Author>
-<Author>Fontecilla-Camps, J.C.</Author>
-</Authors>
-<Citation>Nature 373, 580-587, 1995</Citation>
-<Title>Crystal structure of the nickel-iron hydrogenase from Desulfovibrio gigas.</Title>
-<Xref>DOI:10.1038/373580a0</Xref>
-<Xref>PMID:7854413</Xref>
-<Note>X-ray diffraction, 2.85 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Volbeda, A.</Author>
-<Author>Frey, M.</Author>
-<Author>Fontecilla-Camps, J.C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, March 1996</Citation>
-<Description>Crystal structure of the oxidized form of Ni-Fe hydrogenase.</Description>
-<Xref>PDB:1FRV</Xref>
-<Note>annotation; X-ray diffraction, 2.85 angstroms</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>C, C, C, H</SequenceSpec>
-<Condition>cross-link 4</Condition>
-<Xref>GO:0018303</Xref>
-<Xref>PSI-MOD:00290</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>4Fe-4S</Keyword>
-<Keyword>iron-sulfur protein</Keyword>
-<Keyword>metalloprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="metal__iron-sulfur (4fe-4s)__c">METAL Iron-sulfur (4Fe-4S)</Feature>
-<Feature type="UniProt" key="metal__iron-sulfur (4fe-4s); via pros nitrogen__h">METAL Iron-sulfur (4Fe-4S); via pros nitrogen</Feature>
-</Features>
-<Image src="/images/AA0285.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0285.PDB" />
-</Entry>
-<Entry id="AA0286">
-<Header>
-<Code>AA0286</Code>
-<Dates>
-<CreationDate>17-Mar-2000</CreationDate>
-<StrucRevDate>17-Mar-2000</StrucRevDate>
-<TextChngDate>25-Feb-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>tris-L-cysteinyl L-aspartato tetrairon tetrasulfide</Name>
-<SystematicName>tetra-mu3-sulfidotris(S-cysteinyliron)(O4-aspartatoiron)</SystematicName>
-<Xref>COMe:BIM000061</Xref>
-<Xref>PDBHET:SF4</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 13 Fe 4 H 16 N 4 O 6 S 7</Formula>
-<FormalCharge>2-</FormalCharge>
-<Weight type="chemical">772.09</Weight>
-<Weight type="physical">771.652328</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0004 AA0005 AA0005 AA0005">
-<Formula>C 0 Fe 4 H -4 N 0 O 0 S 4</Formula>
-<FormalCharge>2-</FormalCharge>
-<Weight type="chemical">347.59</Weight>
-<Weight type="physical">347.597831</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gorst, C.M.</Author>
-<Author>Yeh, Y.H.</Author>
-<Author>Teng, Q.</Author>
-<Author>Calzolai, L.</Author>
-<Author>Zhou, Z.H.</Author>
-<Author>Adams, M.W.W.</Author>
-<Author>La Mar, G.N.</Author>
-</Authors>
-<Citation>Biochemistry 34, 600-610, 1995</Citation>
-<Title>[1]H NMR investigation of the paramagnetic cluster environment in Pyrococcus furiosus three-iron ferredoxin: sequence-specific assignment of ligated cysteines independent of tertiary structure.</Title>
-<Xref>DOI:10.1021/bi00002a027</Xref>
-<Xref>PMID:7819255</Xref>
-<Note>conformation, binding site, and disulfide bond assignments by (1)H-NMR</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Zhou, Z.H.</Author>
-<Author>Adams, M.W.W.</Author>
-</Authors>
-<Citation>Biochemistry 36, 10892-10900, 1997</Citation>
-<Title>Site-directed mutations of the 4Fe-ferredoxin from the hyperthermophilic archaeon Pyrococcus furiosus: role of the cluster-coordinating aspartate in physiological electron transfer reactions.</Title>
-<Xref>DOI:10.1021/bi9708141</Xref>
-<Xref>PMID:9283079</Xref>
-<Note>demonstration of aspartate binding</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>C, C, C, D</SequenceSpec>
-<Condition>cross-link 4</Condition>
-<Xref>GO:0018304</Xref>
-<Xref>PSI-MOD:00291</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>4Fe-4S</Keyword>
-<Keyword>iron-sulfur protein</Keyword>
-<Keyword>metalloprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="metal__iron-sulfur (4fe-4s)__d">METAL Iron-sulfur (4Fe-4S)</Feature>
-</Features>
-<Image src="/images/AA0286.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0286.PDB" />
-</Entry>
-<Entry id="AA0287">
-<Header>
-<Code>AA0287</Code>
-<Dates>
-<CreationDate>17-Mar-2000</CreationDate>
-<StrucRevDate>17-Mar-2000</StrucRevDate>
-<TextChngDate>30-Jun-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6-pyruvic acid 2-iminyl-L-lysine</Name>
-<SystematicName>(2S)-2-amino-6-([1-carboxyethylidene]amino)hexanoic acid</SystematicName>
-<Xref>PDBHET:KPI</Xref>
-<Xref>PDBHET:PYR</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 14 N 2 O 3</Formula>
-<Weight type="chemical">198.22</Weight>
-<Weight type="physical">198.100442</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 3 H 2 N 0 O 2</Formula>
-<Weight type="chemical">70.05</Weight>
-<Weight type="physical">70.005479</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Laber, B.</Author>
-<Author>Gomis-Rueth, F.X.</Author>
-<Author>Romao, M.J.</Author>
-<Author>Huber, R.</Author>
-</Authors>
-<Citation>Biochem. J. 288, 691-695, 1992</Citation>
-<Title>Escherichia coli dihydrodipicolinate synthase. Identification of the active site and crystallization.</Title>
-<Xref>PMID:1463470</Xref>
-<Note>evidence for covalent intermediate</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mirwaldt, C.</Author>
-<Author>Korndoerfer, I.</Author>
-<Author>Huber, R.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 246, 227-239, 1995</Citation>
-<Title>The crystal structure of dihydrodipicolinate synthase from Escherichia coli at 2.5 angstroms resolution.</Title>
-<Xref>DOI:10.1006/jmbi.1994.0078</Xref>
-<Xref>PMID:7853400</Xref>
-<Note>X-ray diffraction, 2.5 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mirwaldt, C.</Author>
-<Author>Korndoerfer, I.</Author>
-<Author>Huber, R.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, February 1995</Citation>
-<Description>Dihydrodipicolinate synthase.</Description>
-<Xref>PDB:1DHP</Xref>
-<Note>X-ray diffraction, 2.5 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lawrence, M.C.</Author>
-<Author>Barbosa, J.A.R.G.</Author>
-<Author>Smith, B.J.</Author>
-<Author>Hall, N.E.</Author>
-<Author>Pilling, P.A.</Author>
-<Author>Ooi, H.C.</Author>
-<Author>Marcuccio, S.M.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, July 1996</Citation>
-<Description>N-Acetylneuraminate lyase in complex with hydroxypyruvate.</Description>
-<Xref>PDB:1FDY</Xref>
-<Note>X-ray diffraction, 2.45 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lawrence, M.C.</Author>
-<Author>Barbosa, J.A.R.G.</Author>
-<Author>Smith, B.J.</Author>
-<Author>Hall, N.E.</Author>
-<Author>Pilling, P.A.</Author>
-<Author>Ooi, H.C.</Author>
-<Author>Marcuccio, S.M.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 266, 381-399, 1997</Citation>
-<Title>Structure and mechanism of a sub-family of enzymes related to N-acetylneuraminate lyase.</Title>
-<Xref>DOI:10.1006/jmbi.1996.0769</Xref>
-<Xref>PMID:9047371</Xref>
-<Note>X-ray diffraction, 2.45 angstroms</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>GO:0018308</Xref>
-<Xref>PSI-MOD:00292</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="act_site____k">ACT_SITE</Feature>
-<Feature type="UniProt" key="act_site__schiff-base intermediate with substrate__k">ACT_SITE Schiff-base intermediate with substrate</Feature>
-</Features>
-<Image src="/images/AA0287.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0287.PDB" />
-</Entry>
-<Entry id="AA0288">
-<Header>
-<Code>AA0288</Code>
-<Dates>
-<CreationDate>20-Apr-2000</CreationDate>
-<StrucRevDate>20-Apr-2000</StrucRevDate>
-<TextChngDate>31-May-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>tris-L-cysteinyl L-serinyl tetrairon tetrasulfide</Name>
-<SystematicName>tetra-mu3-sulfidotris(S-cysteinyliron)(O3-serinyliron)</SystematicName>
-<Xref>PDBHET:SF4</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 12 Fe 4 H 16 N 4 O 5 S 7</Formula>
-<FormalCharge>2-</FormalCharge>
-<Weight type="chemical">744.08</Weight>
-<Weight type="physical">743.657414</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005 AA0005 AA0016">
-<Formula>C 0 Fe 4 H -4 N 0 O 0 S 4</Formula>
-<FormalCharge>2-</FormalCharge>
-<Weight type="chemical">347.59</Weight>
-<Weight type="physical">347.597831</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mansy, S.S.</Author>
-<Author>Xiong, Y.</Author>
-<Author>Hemann, C.</Author>
-<Author>Hille, R.</Author>
-<Author>Sundaralingam, M.</Author>
-<Author>Cowan, J.A.</Author>
-</Authors>
-<Citation>Biochemistry 41, 1195-1201, 2002</Citation>
-<Title>Crystal structure and stability studies of C77S HiPIP: a serine ligated [4Fe-4S] cluster.</Title>
-<Xref>PMID:11802718</Xref>
-<Note>X-ray diffraction, 1.90 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mansy, S.S.</Author>
-<Author>Xiong, Y.</Author>
-<Author>Hemann, C.</Author>
-<Author>Hille, R.</Author>
-<Author>Sundaralingam, M.</Author>
-<Author>Cowan, J.A.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, August 2001</Citation>
-<Description>Crystal structure of C77S HIPIP: a serine ligated [4Fe-4S] cluster.</Description>
-<Xref>PDB:1JS2</Xref>
-<Note>X-ray diffraction, 1.90 angstroms</Note>
-</ReferenceBlock>
-<Comment>The occurrence of serine rather than cysteine in an otherwise strongly conserved homology domain known to bind the 4Fe-4S cluster in other proteins suggested that serine might also bind iron-sulfur clusters. The engineered replacement of a cysteine ligand to a [4Fe-4S] cluster with serine resulted in a ligand bond that was 0.11 angstroms shorter. However, the cluster was less stable because of increased sensitivity to proton mediated solvolysis.</Comment>
-<SequenceCode>
-<SequenceSpec>C, C, C, S</SequenceSpec>
-<Condition>cross-link 4</Condition>
-<Xref>GO:0018305</Xref>
-<Xref>PSI-MOD:00293</Xref>
-</SequenceCode>
-<Source>deprecated</Source>
-<Keywords>
-<Keyword>4Fe-4S</Keyword>
-<Keyword>iron-sulfur protein</Keyword>
-<Keyword>metalloprotein</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0288.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0288.PDB" />
-</Entry>
-<Entry id="AA0289">
-<Header>
-<Code>AA0289</Code>
-<Dates>
-<CreationDate>20-Apr-2000</CreationDate>
-<StrucRevDate>20-Apr-2000</StrucRevDate>
-<TextChngDate>25-Feb-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>bis-L-cysteinyl L-N3'-histidino L-serinyl tetrairon tetrasulfide</Name>
-<SystematicName>tetra-mu3-sulfidobis(S-cysteinyliron)(N3'-histidinoiron)(O3-serinyliron)</SystematicName>
-<Xref>PDBHET:SF4</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 15 Fe 4 H 18 N 6 O 5 S 6</Formula>
-<FormalCharge>2-</FormalCharge>
-<Weight type="chemical">778.09</Weight>
-<Weight type="physical">777.707141</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005 AA0009 AA0016">
-<Formula>C 0 Fe 4 H -4 N 0 O 0 S 4</Formula>
-<FormalCharge>2-</FormalCharge>
-<Weight type="chemical">347.59</Weight>
-<Weight type="physical">347.597831</Weight>
-</CorrectionBlock>
-<Comment>The occurrence of serine rather than cysteine in an otherwise strongly conserved homology domain known to bind the 4Fe-4S cluster in other proteins suggests that serine may also bind iron-sulfur clusters.</Comment>
-<SequenceCode>
-<SequenceSpec>C, C, H, S</SequenceSpec>
-<Condition>cross-link 4</Condition>
-<Xref>GO:0018306</Xref>
-<Xref>PSI-MOD:00294</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>4Fe-4S</Keyword>
-<Keyword>iron-sulfur protein</Keyword>
-<Keyword>metalloprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="metal__iron-sulfur (4fe-4s)__s">METAL Iron-sulfur (4Fe-4S)</Feature>
-<Feature type="UniProt" key="metal__iron-sulfur (4fe-4s); via pros nitrogen__h">METAL Iron-sulfur (4Fe-4S); via pros nitrogen</Feature>
-</Features>
-<Image src="/images/AA0289.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0289.PDB" />
-</Entry>
-<Entry id="AA0290">
-<Header>
-<Code>AA0290</Code>
-<Dates>
-<CreationDate>16-Jun-2000</CreationDate>
-<StrucRevDate>16-Jun-2000</StrucRevDate>
-<TextChngDate>25-Feb-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-octanoyl-L-serine</Name>
-<AlternateName>L-serine octanoate ester</AlternateName>
-<AlternateName>O3-octanoyl-L-serine</AlternateName>
-<SystematicName>(2S)-2-amino-3-(octanoyloxy)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 11 H 19 N 1 O 3</Formula>
-<Weight type="chemical">213.28</Weight>
-<Weight type="physical">213.136493</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 8 H 14 N 0 O 1</Formula>
-<Weight type="chemical">126.20</Weight>
-<Weight type="physical">126.104465</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kojima, M.</Author>
-<Author>Hosoda, H.</Author>
-<Author>Date, Y.</Author>
-<Author>Nakazato, M.</Author>
-<Author>Matsuo, H.</Author>
-<Author>Kangawa, K.</Author>
-</Authors>
-<Citation>Nature 402, 656-660, 1999</Citation>
-<Title>Ghrelin is a growth-hormone-releasing acylated peptide from stomach.</Title>
-<Xref>DOI:10.1038/45230</Xref>
-<Xref>PMID:10604470</Xref>
-<Note>chromatographic and mass spectrometric identification; chemical synthesis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yang, J.</Author>
-<Author>Brown, M.S.</Author>
-<Author>Liang, G.</Author>
-<Author>Grishin, N.V.</Author>
-<Author>Goldstein, J.L.</Author>
-</Authors>
-<Citation>Cell 132, 387-396, 2008</Citation>
-<Title>Identification of the acyltransferase that octanoylates ghrelin, an appetite-stimulating peptide hormone.</Title>
-<Xref>DOI:10.1016/j.cell.2008.01.017</Xref>
-<Xref>PMID:18267071</Xref>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>ghrelin O-acyltransferase, GOAT (EC 2.3.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>GO:0018191</Xref>
-<Xref>GO:0042050</Xref>
-<Xref>PSI-MOD:00295</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lipoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__o-octanoyl serine__s">LIPID O-octanoyl serine</Feature>
-</Features>
-<Image src="/images/AA0290.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0290.PDB" />
-</Entry>
-<Entry id="AA0291">
-<Header>
-<Code>AA0291</Code>
-<Dates>
-<CreationDate>31-Mar-2001</CreationDate>
-<StrucRevDate>31-Mar-2001</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-D-glucuronosyl-L-serine</Name>
-<AlternateName>O3-D-glucuronosyl-L-serine</AlternateName>
-<SystematicName>(2S)-2-amino-3-(beta-D-glucopyranuronosyl)propanoic acid</SystematicName>
-<Xref>CAS:528-16-5</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 13 N 1 O 8</Formula>
-<Weight type="chemical">263.20</Weight>
-<Weight type="physical">263.064116</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 6 H 8 N 0 O 6</Formula>
-<Weight type="chemical">176.12</Weight>
-<Weight type="physical">176.032088</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Jonsson, A.P.</Author>
-<Author>Griffiths, W.J.</Author>
-<Author>Bratt, P.</Author>
-<Author>Johansson, I.</Author>
-<Author>Stroemberg, N.</Author>
-<Author>Joernvall, H.</Author>
-<Author>Bergman, T.</Author>
-</Authors>
-<Citation>FEBS Lett. 475, 131-134, 2000</Citation>
-<Title>A novel Ser O-glucuronidation in acidic proline-rich proteins identified by tandem mass spectrometry.</Title>
-<Xref>DOI:10.1016/S0014-5793(00)01645-8</Xref>
-<Xref>PMID:10858503</Xref>
-<Note>neither the identity of the hexuronic acid nor the mode of linkage is definitively established</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Vitorino, R.</Author>
-<Author>Alves, R.</Author>
-<Author>Barros, A.</Author>
-<Author>Caseiro, A.</Author>
-<Author>Ferreira, R.</Author>
-<Author>Lobo, M.C.</Author>
-<Author>Bastos, A.</Author>
-<Author>Duarte, J.</Author>
-<Author>Carvalho, D.</Author>
-<Author>Santos, L.L.</Author>
-<Author>Amado, F.L.</Author>
-</Authors>
-<Citation>Proteomics 10, 3732-3742, 2010</Citation>
-<Title>Finding new posttranslational modifications in salivary proline-rich proteins.</Title>
-<Xref>DOI:10.1002/pmic.201000261</Xref>
-<Xref>PMID:20879038</Xref>
-<Note>mass spectrometric detection</Note>
-</ReferenceBlock>
-<Comment>The beta glucuronosyl form is shown.</Comment>
-<Comment>See also RESID:AA0154, RESID:AA0208, RESID:AA0209, RESID:AA0210, RESID:AA0296, RESID:AA0297, RESID:AA0397, RESID:AA0398, RESID:AA0400, RESID:AA0402, RESID:AA0404, RESID:AA0406, and RESID:AA0422 for other O-glycosylated serines.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>UDP-glucuronate beta-D-glucuronosyltransferase (acceptor-unspecific) (EC 2.4.1.17)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>GO:0018413</Xref>
-<Xref>PSI-MOD:00296</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__o-linked (glca) serine__s">CARBOHYD O-linked (GlcA) serine</Feature>
-</Features>
-<Image src="/images/AA0291.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0291.PDB" />
-</Entry>
-<Entry id="AA0292">
-<Header>
-<Code>AA0292</Code>
-<Dates>
-<CreationDate>31-Mar-2001</CreationDate>
-<StrucRevDate>31-Mar-2001</StrucRevDate>
-<TextChngDate>31-Mar-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>tris-L-cysteinyl L-cysteine persulfido bis-L-glutamato L-histidino nickel triiron disulfide trioxide</Name>
-<AlternateName>carbon monoxide dehydrogenase nickel-iron cofactor</AlternateName>
-<AlternateName>hybrid nickel-triiron cluster</AlternateName>
-<AlternateName>Ni-3Fe-2S-3O cluster</AlternateName>
-<SystematicName>mu-1:2kappaO-oxido-mu-1:3kappaO-oxido-mu-2:4kappaO-oxido-mu-3:4kappaS-sulfido-mu3-2:3:4kappaS-sulfido-S-cysteinyl-N1'-histidino-O5-glutamato 1-iron-S5-cysteine persulfido-O5-glutamato 2-nickel-3,4-bis-(S-cysteinyl iron)</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 28 Fe 3 H 34 N 9 Ni 1 O 14 S 7</Formula>
-<Weight type="chemical">1171.28</Weight>
-<Weight type="physical">1169.767174</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0009 AA0006 AA0005 AA0005 AA0005 AA0005 AA0006">
-<Formula>C 0 Fe 3 H -7 N 0 Ni 1 O 3 S 3</Formula>
-<Weight type="chemical">363.35</Weight>
-<Weight type="physical">362.586337</Weight>
-</CorrectionBlock>
-<Comment>This one nickel, three iron cluster with mixed ligands is now thought not to exist. See RESID:AA0310.</Comment>
-<SequenceCode>
-<SequenceSpec>C, C, C, C, E, E, H</SequenceSpec>
-<Condition>cross-link 7</Condition>
-<Condition>secondary to RESID:AA0269</Condition>
-<Xref>GO:0018415</Xref>
-<Xref>GO:0018416</Xref>
-<Xref>PSI-MOD:00297</Xref>
-</SequenceCode>
-<Source>deprecated</Source>
-<Keywords>
-<Keyword>iron-sulfur protein</Keyword>
-<Keyword>metalloprotein</Keyword>
-<Keyword>Ni-3Fe-2S-3O</Keyword>
-<Keyword>nickel</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this dubious modification is not currently annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0292.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0292.PDB" />
-</Entry>
-<Entry id="AA0293">
-<Header>
-<Code>AA0293</Code>
-<Dates>
-<CreationDate>31-Mar-2001</CreationDate>
-<StrucRevDate>31-Mar-2001</StrucRevDate>
-<TextChngDate>31-Mar-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>tris-L-cysteinyl L-cysteine persulfido L-glutamato L-histidino L-serinyl nickel triiron disulfide trioxide</Name>
-<AlternateName>carbon monoxide dehydrogenase nickel-iron cofactor</AlternateName>
-<AlternateName>hybrid nickel-triiron cluster</AlternateName>
-<AlternateName>Ni-3Fe-2S-3O cluster</AlternateName>
-<SystematicName>mu-1:2kappaO-oxido-mu-1:3kappaO-oxido-mu-2:4kappaO-oxido-mu-3:4kappaS-sulfido-mu3-2:3:4kappaS-sulfido-S-cysteinyl-N1'-histidino-O5-glutamato 1-iron-S5-cysteine persulfido-O3-serinyl 2-nickel-3,4-bis-(S-cysteinyl iron)</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 26 Fe 3 H 32 N 9 Ni 1 O 13 S 7</Formula>
-<Weight type="chemical">1129.24</Weight>
-<Weight type="physical">1127.756609</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0009 AA0006 AA0005 AA0005 AA0005 AA0005 AA0016">
-<Formula>C 0 Fe 3 H -7 N 0 Ni 1 O 3 S 3</Formula>
-<Weight type="chemical">363.35</Weight>
-<Weight type="physical">362.586337</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Stephens, P.J.</Author>
-<Author>McKenna, M.C.</Author>
-<Author>Ensign, S.A.</Author>
-<Author>Bonam, D.</Author>
-<Author>Ludden, P.W.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 264, 16347-16350, 1989</Citation>
-<Title>Identification of a Ni- and Fe-containing cluster in Rhodospirillum rubrum carbon monoxide dehydrogenase.</Title>
-<Xref>PMID:2550436</Xref>
-</ReferenceBlock>
-<Comment>This one nickel, three iron cluster with mixed ligands is now thought not to exist. See RESID:AA0310.</Comment>
-<SequenceCode>
-<SequenceSpec>C, C, C, C, E, H, S</SequenceSpec>
-<Condition>cross-link 7</Condition>
-<Condition>secondary to RESID:AA0269</Condition>
-<Xref>GO:0018417</Xref>
-<Xref>GO:0018418</Xref>
-<Xref>PSI-MOD:00298</Xref>
-</SequenceCode>
-<Source>deprecated</Source>
-<Keywords>
-<Keyword>iron-sulfur protein</Keyword>
-<Keyword>metalloprotein</Keyword>
-<Keyword>Ni-3Fe-2S-3O</Keyword>
-<Keyword>nickel</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this dubious modification is not currently annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0293.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0293.PDB" />
-</Entry>
-<Entry id="AA0294">
-<Header>
-<Code>AA0294</Code>
-<Dates>
-<CreationDate>31-Mar-2001</CreationDate>
-<StrucRevDate>31-Mar-2001</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6-(L-isoaspartyl)-L-lysine</Name>
-<AlternateName>beta-(N6-lysyl)aspartyl acid</AlternateName>
-<AlternateName>isoaspartyl N6-lysine</AlternateName>
-<AlternateName>N(epsilon)-(beta-aspartyl)lysine</AlternateName>
-<SystematicName>(2S)-2-amino-6-([(3S)-3-amino-3-carboxypropanoyl]amino)hexanoic acid</SystematicName>
-<Xref>CAS:5853-83-8</Xref>
-<Xref>ChEBI:21862</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 10 H 15 N 3 O 3</Formula>
-<Weight type="chemical">225.25</Weight>
-<Weight type="physical">225.111341</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0003 AA0012" label="ASN">
-<Formula>C 0 H -3 N -1 O 0</Formula>
-<Weight type="chemical">-17.03</Weight>
-<Weight type="physical">-17.026549</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0004 AA0012" label="ASP">
-<Formula>C 0 H -2 N 0 O -1</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Klostermeyer, H.</Author>
-</Authors>
-<Citation>Meth. Enzymol. 107, 258-261, 1984</Citation>
-<Title>Nepsilon-(beta-Aspartyl)lysine.</Title>
-<Xref>DOI:10.1016/0076-6879(84)07016-6</Xref>
-<Xref>PMID:6503713</Xref>
-<Note>review; discussion of occurrence as an excretion product from an unknown metabolic or dietary source</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wikoff, W.R.</Author>
-<Author>Liljas, L.</Author>
-<Author>Duda, R.L.</Author>
-<Author>Tsuruta, H.</Author>
-<Author>Hendrix, R.W.</Author>
-<Author>Johnson, J.E.</Author>
-</Authors>
-<Citation>Science 289, 2129-2133, 2000</Citation>
-<Title>Topologically linked protein rings in the bacteriophage HK97 capsid.</Title>
-<Xref>DOI:10.1126/science.289.5487.2129</Xref>
-<Xref>PMID:11000116</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Osička, R.</Author>
-<Author>Procházková, K.</Author>
-<Author>Šulc, M.</Author>
-<Author>Linhartová, I.</Author>
-<Author>Havlíček, V.</Author>
-<Author>Šebo, P.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 279, 24944-24956, 2004</Citation>
-<Title>A novel &quot;clip-and-link&quot; activity of repeat in toxin (RTX) proteins from gram-negative pathogens. Covalent protein cross-linking by an Asp-Lys isopeptide bond upon calcium-dependent processing at an Asp-Pro bond.</Title>
-<Xref>DOI:10.1074/jbc.M314013200</Xref>
-<Xref>PMID:15044436</Xref>
-<Note>chemical characterization and mass spectrometric identification; directed mutation analysis; it was not determined whether the cross-links were through the aspartyl C1 or C4 carboxyl, and both are probably formed, see also RESID:AA0583; the encoding of an author's name in the PubMed citation is corrected to UTF8</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kang, H.J.</Author>
-<Author>Coulibaly, F.</Author>
-<Author>Clow, F.</Author>
-<Author>Proft, T.</Author>
-<Author>Baker, E.N.</Author>
-</Authors>
-<Citation>Science 318, 1625-1628, 2007</Citation>
-<Title>Stabilizing isopeptide bonds revealed in gram-positive bacterial pilus structure.</Title>
-<Xref>DOI:10.1126/science.1145806</Xref>
-<Xref>PMID:18063798</Xref>
-<Note>X-ray diffraction, 2.2 angstroms; evidence for multiple intrachain isoaspartyl lysine isopeptide cross-links</Note>
-</ReferenceBlock>
-<SequenceCode link="ASN">
-<SequenceSpec>K, N</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>GO:0018420</Xref>
-<Xref>GO:0019937</Xref>
-<Xref>GO:0019938</Xref>
-<Xref>PSI-MOD:00299</Xref>
-</SequenceCode>
-<SequenceCode link="ASP">
-<SequenceSpec>D, K</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:01917</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>isopeptide bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__isoaspartyl lysine isopeptide (lys-asn)__k__n" link="ASN">CROSSLNK Isoaspartyl lysine isopeptide (Lys-Asn)</Feature>
-<Feature type="UniProt" key="crosslnk__isoaspartyl lysine isopeptide (asn-lys) (interchain with k-__n" link="ASN">CROSSLNK Isoaspartyl lysine isopeptide (Asn-Lys) (interchain with K-...)</Feature>
-<Feature type="UniProt" key="crosslnk__isoaspartyl lysine isopeptide (lys-asn) (interchain with n-__k" link="ASN">CROSSLNK Isoaspartyl lysine isopeptide (Lys-Asn) (interchain with N-...)</Feature>
-<Feature type="UniProt" key="crosslnk__isoaspartyl lysine isopeptide (asp-lys) (interchain with k-__d" link="ASP">CROSSLNK Isoaspartyl lysine isopeptide (Asp-Lys) (interchain with K-...)</Feature>
-<Feature type="UniProt" key="crosslnk__isoaspartyl lysine isopeptide (lys-asp) (interchain with d-__k" link="ASP">CROSSLNK Isoaspartyl lysine isopeptide (Lys-Asp) (interchain with D-...)</Feature>
-<Feature type="UniProt" key="crosslnk__isoaspartyl lysine isopeptide (lys-asp)__k__d" link="ASP">CROSSLNK Isoaspartyl lysine isopeptide (Lys-Asp)</Feature>
-</Features>
-<Image src="/images/AA0294.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0294.PDB" />
-</Entry>
-<Entry id="AA0295">
-<Header>
-<Code>AA0295</Code>
-<Dates>
-<CreationDate>04-May-2001</CreationDate>
-<StrucRevDate>04-May-2001</StrucRevDate>
-<TextChngDate>30-Sep-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-glutamyl-5-poly(ADP-ribose)</Name>
-<AlternateName>L-isoglutamyl-poly(ADP-ribose)</AlternateName>
-<SystematicName>(S)-2-amino-5-poly[2'-adenosine 5'-(trihydrogen diphosphate) 5'-&gt;5'-ester with 1alpha-D-ribofuranosyl]oxy-5-oxopentanoic acid</SystematicName>
-<Xref>CAS:26656-46-2</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 20 H 28 N 6 O 16 P 2 +</Formula>
-<Weight type="chemical">670.42 +</Weight>
-<Weight type="physical">670.103702 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0006">
-<Formula>C 15 H 21 N 5 O 13 P 2 +</Formula>
-<Weight type="chemical">541.30 +</Weight>
-<Weight type="physical">541.061109 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Smith, S.</Author>
-</Authors>
-<Citation>Trends Biochem. Sci. 26, 174-179, 2001</Citation>
-<Title>The world according to PARP.</Title>
-<Xref>DOI:10.1016/S0968-0004(00)01780-1</Xref>
-<Xref>PMID:11246023</Xref>
-<Note>review</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lindahl, T.</Author>
-<Author>Satoh, M.S.</Author>
-<Author>Poirier, G.G.</Author>
-<Author>Klungland, A.</Author>
-</Authors>
-<Citation>Trends Biochem. Sci. 20, 405-411, 1995</Citation>
-<Title>Post-translational modification of poly(ADP-ribose) polymerase induced by DNA strand breaks.</Title>
-<Xref>DOI:10.1016/S0968-0004(00)89089-1</Xref>
-<Xref>PMID:8533153</Xref>
-<Note>review</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Matic, I.</Author>
-<Author>Ahel, I.</Author>
-<Author>Hay, R.T.</Author>
-</Authors>
-<Citation>Nature Methods 9, 771-772, 2012</Citation>
-<Title>Reanalysis of phosphoproteomics data uncovers ADP-ribosylation sites.</Title>
-<Xref>DOI:10.1038/nmeth.2106</Xref>
-<Xref>PMID:22847107</Xref>
-<Note>mass spectrometric detection of modification by mono-ADPR in reanalysis of phosphoproteomics data</Note>
-</ReferenceBlock>
-<Comment>The alpha form is presented.</Comment>
-<Comment>This entry represents modification by one or more subunits of ADP-ribose.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>NAD+ ADP-ribosyltransferase (EC 2.4.2.30)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>E</SequenceSpec>
-<Xref>GO:0006471</Xref>
-<Xref>GO:0018424</Xref>
-<Xref>PSI-MOD:00300</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>phosphoprotein</Keyword>
-<Keyword>poly adenosine diphosphate ribose</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__polyadp-ribosyl glutamic acid__e">MOD_RES PolyADP-ribosyl glutamic acid</Feature>
-</Features>
-<Image src="/images/AA0295.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0295.PDB" />
-</Entry>
-<Entry id="AA0296">
-<Header>
-<Code>AA0296</Code>
-<Dates>
-<CreationDate>08-Jun-2001</CreationDate>
-<StrucRevDate>08-Jun-2001</StrucRevDate>
-<TextChngDate>20-Apr-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-(N-acetylglucosamine-1-phosphoryl)-L-serine</Name>
-<AlternateName>O-beta(N-acetyl-glucosamine-alpha1-phosphate)serine</AlternateName>
-<AlternateName>O3-(N-acetylglucosamine-1-phosphoryl)-L-serine</AlternateName>
-<AlternateName>O3-L-serine 2-(acetylamino)-2-deoxy-D-glucopyranose 1-phosphodiester</AlternateName>
-<SystematicName>(2S)-2-amino-3-[([(2-acetamido-2-deoxy-alpha-D-glucopyranosyl)oxy][hydroxy]phosphoryl)oxy]propanoic acid</SystematicName>
-<Xref>CAS:6866-69-9</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 11 H 19 N 2 O 10 P 1</Formula>
-<Weight type="chemical">370.25</Weight>
-<Weight type="physical">370.077731</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 8 H 14 N 1 O 8 P 1</Formula>
-<Weight type="chemical">283.17</Weight>
-<Weight type="physical">283.045703</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gustafson, G.L.</Author>
-<Author>Milner, L.A.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 255, 7208-7210, 1980</Citation>
-<Title>Occurrence of N-acetylglucosamine-1-phosphate in proteinase I from Dictyostelium discoideum.</Title>
-<Xref>PMID:6993483</Xref>
-<Note>chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gustafson, G.L.</Author>
-<Author>Gander, J.E.</Author>
-</Authors>
-<Citation>Meth. Enzymol. 107, 172-183, 1984</Citation>
-<Title>O beta-(N-acetyl-alpha-glucosamine-1-phosphoryl)serine in proteinase I from Dictyostelium discoideum.</Title>
-<Xref>DOI:10.1016/0076-6879(84)07011-7</Xref>
-<Xref>PMID:6438439</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mehta, D.P.</Author>
-<Author>Ichikawa, M.</Author>
-<Author>Salimath, P.V.</Author>
-<Author>Etchison, J.R.</Author>
-<Author>Haak, R.</Author>
-<Author>Manzi, A.</Author>
-<Author>Freeze, H.H.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 271, 10897-10903, 1996</Citation>
-<Title>A lysosomal cysteine proteinase from Dictyostelium discoideum contains N-acetylglucosamine-1-phosphate bound to serine but not mannose-6-phosphate on N-linked oligosaccharides.</Title>
-<Xref>DOI:10.1074/jbc.271.18.10897</Xref>
-<Xref>PMID:8631906</Xref>
-</ReferenceBlock>
-<Comment>See also RESID:AA0154, RESID:AA0208, RESID:AA0209, RESID:AA0210, RESID:AA0291, RESID:AA0297, RESID:AA0397, RESID:AA0398, RESID:AA0400, RESID:AA0402, RESID:AA0404, RESID:AA0406, and RESID:AA0422 for other O-glycosylated serines.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>UDP-N-acetylglucosamine:serine-protein N-acetylglucosamine-1-phosphotransferase (EC 2.7.8.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>GO:0018425</Xref>
-<Xref>PSI-MOD:00301</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0296.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0296.PDB" />
-</Entry>
-<Entry id="AA0297">
-<Header>
-<Code>AA0297</Code>
-<Dates>
-<CreationDate>08-Jun-2001</CreationDate>
-<StrucRevDate>30-Jun-2006</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-(D-mannose-1-phosphoryl)-L-serine</Name>
-<AlternateName>O-(alpha-D-mannosyl-1-phosphoryl)-L-serine</AlternateName>
-<AlternateName>O3-(D-mannose-1-phosphoryl)-L-serine</AlternateName>
-<AlternateName>O3-L-serine alpha-D-mannopyranose 1-phosphodiester</AlternateName>
-<SystematicName>O-[alpha-D-mannopyranosyloxy(hydroxy)phosphoryl]-L-serine</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 16 N 1 O 10 P 1 +</Formula>
-<Weight type="chemical">329.20 +</Weight>
-<Weight type="physical">329.051182 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 6 H 11 N 0 O 8 P 1 +</Formula>
-<Weight type="chemical">242.12 +</Weight>
-<Weight type="physical">242.019154 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Moss, J.M.</Author>
-<Author>Reid, G.E.</Author>
-<Author>Mullin, K.A.</Author>
-<Author>Zawadzki, J.L.</Author>
-<Author>Simpson, R.J.</Author>
-<Author>McConville, M.J.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 274, 6678-6688, 1999</Citation>
-<Title>Characterization of a novel GDP-mannose:Serine-protein mannose-1-phosphotransferase from Leishmania mexicana.</Title>
-<Xref>DOI:10.1074/jbc.274.10.6678</Xref>
-<Xref>PMID:10037765</Xref>
-<Note>biosynthesis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Macrae, J.I.</Author>
-<Author>Acosta-Serrano, A.</Author>
-<Author>Morrice, N.A.</Author>
-<Author>Mehlert, A.</Author>
-<Author>Ferguson, M.A.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 280, 12201-12211, 2005</Citation>
-<Title>Structural characterization of NETNES, a novel glycoconjugate in Trypanosoma cruzi epimastigotes.</Title>
-<Xref>DOI:10.1074/jbc.M412939200</Xref>
-<Xref>PMID:15649890</Xref>
-</ReferenceBlock>
-<Comment>Mannose oligosaccharides and short phosphoglycan chains may be attached to the mannose 1-phosphate at the 2 position.</Comment>
-<Comment>See also RESID:AA0154, RESID:AA0208, RESID:AA0209, RESID:AA0210, RESID:AA0291, RESID:AA0296, RESID:AA0397, RESID:AA0398, RESID:AA0400, RESID:AA0402, RESID:AA0404, RESID:AA0406, and RESID:AA0422 for other O-glycosylated serines.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>GDP-mannose:serine-protein mannose-1-phosphotransferase (EC 2.7.8.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>GO:0018426</Xref>
-<Xref>PSI-MOD:00302</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__o-linked (p-man...) serine__s">CARBOHYD O-linked (P-Man...) serine</Feature>
-</Features>
-<Image src="/images/AA0297.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0297.PDB" />
-</Entry>
-<Entry id="AA0298">
-<Header>
-<Code>AA0298</Code>
-<Dates>
-<CreationDate>08-Jun-2001</CreationDate>
-<StrucRevDate>08-Jun-2001</StrucRevDate>
-<TextChngDate>31-Dec-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>heptakis-L-histidino tetracopper mu4-sulfide hydroxide</Name>
-<AlternateName>nitrous oxide reductase nosZ CuZ cluster</AlternateName>
-<AlternateName>pentakis-L-N1'-histidino-bis-L-N3'-histidino tetracopper sulfide hydroxide</AlternateName>
-<SystematicName>mu4-sulfido bis(bis-N1'-histidino copper)(N1'-histidino-N3'-histidino copper)(N3'-histidino hydroxide copper)</SystematicName>
-<Xref>COMe:BIM000109</Xref>
-<Xref>PDBHET:CUZ</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 42 Cu 4 H 43 N 21 O 8 S 1</Formula>
-<Weight type="chemical">1256.19</Weight>
-<Weight type="physical">1253.050808</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0009 AA0009 AA0009 AA0009 AA0009 AA0009 AA0009">
-<Formula>C 0 Cu 4 H -6 N 0 O 1 S 1</Formula>
-<Weight type="chemical">296.19</Weight>
-<Weight type="physical">293.638425</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Rasmussen, T.</Author>
-<Author>Berks, B.C.</Author>
-<Author>Sanders-Loehr, J.</Author>
-<Author>Dooley, D.M.</Author>
-<Author>Zumft, W.G.</Author>
-<Author>Thomson, A.J.</Author>
-</Authors>
-<Citation>Biochemistry 39, 12753-12756, 2000</Citation>
-<Title>The catalytic center in nitrous oxide reductase, CuZ, is a copper-sulfide cluster.</Title>
-<Xref>DOI:10.1021/bi001811i</Xref>
-<Xref>PMID:11041839</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Brown, K.</Author>
-<Author>Djinovic-Carugo, K.</Author>
-<Author>Haltia, T.</Author>
-<Author>Cabrito, I.</Author>
-<Author>Saraste, M.</Author>
-<Author>Moura, J.J.</Author>
-<Author>Moura, I.</Author>
-<Author>Tegoni, M.</Author>
-<Author>Cambillau, C.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 275, 41133-41136, 2000</Citation>
-<Title>Revisiting the catalytic CuZ cluster of nitrous oxide (N2O) reductase. Evidence of a bridging inorganic sulfur.</Title>
-<Xref>DOI:10.1074/jbc.M008617200</Xref>
-<Xref>PMID:11024061</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Brown, K.</Author>
-<Author>Tegoni, M.</Author>
-<Author>Cambillau, C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, October 1999</Citation>
-<Description>Crystal structure of nitrous oxide reductase from Pseudomonas nautica, at 2.4A resolution.</Description>
-<Xref>PDB:1QNI</Xref>
-<Note>X-ray diffraction, 2.40 angstroms</Note>
-</ReferenceBlock>
-<Comment>The hydroxide is probably replaced by the nitrous oxide substrate. An undetermined number of the histidine ligands are protonated and there is, as yet, no evidence for calculation of the formal charge.</Comment>
-<SequenceCode>
-<SequenceSpec>H, H, H, H, H, H, H</SequenceSpec>
-<Condition>cross-link 7</Condition>
-<Xref>GO:0018429</Xref>
-<Xref>PSI-MOD:00303</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>copper</Keyword>
-<Keyword>metalloprotein</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt" key="metal__copper z__h">METAL Copper Z</Feature>
-<Note>this UniProt feature has a structural misrepresentation</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0298.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0298.PDB" />
-</Entry>
-<Entry id="AA0299">
-<Header>
-<Code>AA0299</Code>
-<Dates>
-<CreationDate>30-Jun-2001</CreationDate>
-<StrucRevDate>30-Jun-2001</StrucRevDate>
-<TextChngDate>31-Dec-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-leucine methyl ester</Name>
-<AlternateName>2-amino-4-methylpentanoic methyl ester</AlternateName>
-<AlternateName>alpha-aminoisocaproic methyl ester</AlternateName>
-<AlternateName>methyl L-leucinate</AlternateName>
-<SystematicName>methyl (2S)-2-amino-4-methylpentanoate</SystematicName>
-<Xref>CAS:2666-93-5</Xref>
-<Xref>ChEBI:44075</Xref>
-<Xref>PDBHET:MLL</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 14 N 1 O 2</Formula>
-<Weight type="chemical">144.19</Weight>
-<Weight type="physical">144.102454</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0011">
-<Formula>C 1 H 2 N 0 O 0</Formula>
-<Weight type="chemical">14.03</Weight>
-<Weight type="physical">14.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Xie, H.</Author>
-<Author>Clarke, S.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 268, 13364-13371, 1993</Citation>
-<Title>Methyl esterification of C-terminal leucine residues in cytosolic 36-kDa polypeptides of bovine brain. A novel eucaryotic protein carboxyl methylation reaction.</Title>
-<Xref>PMID:8514774</Xref>
-<Note>radiolabeling and enzymatic evidence for carboxyl methylation of the C-terminal leucine of an unidentified cytoplasmic protein</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Favre, B.</Author>
-<Author>Zolnierowicz, S.</Author>
-<Author>Turowski, P.</Author>
-<Author>Hemmings, B.A.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 269, 16311-16317, 1994</Citation>
-<Title>The catalytic subunit of protein phosphatase 2A is carboxyl-methylated in vivo.</Title>
-<Xref>PMID:8206937</Xref>
-<Note>chemical and immunological characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bryant, J.C.</Author>
-<Author>Westphal, R.S.</Author>
-<Author>Wadzinski, B.E.</Author>
-</Authors>
-<Citation>Biochem. J. 339, 241-246, 1999</Citation>
-<Title>Methylated C-terminal leucine residue of PP2A catalytic subunit is important for binding of regulatory Balpha subunit.</Title>
-<Xref>DOI:10.1042/0264-6021:3390241</Xref>
-<Xref>PMID:10191253</Xref>
-<Note>biochemical role of modification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Cho, U.S.</Author>
-<Author>Xu, W.</Author>
-</Authors>
-<Citation>Nature 445, 53-57, 2007</Citation>
-<Title>Crystal structure of a protein phosphatase 2A heterotrimeric holoenzyme.</Title>
-<Xref>DOI:10.1038/nature05351</Xref>
-<Xref>PMID:17086192</Xref>
-<Note>X-ray diffraction, 3.50 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>CHO, U.S.</Author>
-<Author>XU, W.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, September 2006</Citation>
-<Description>Crystal structure of a protein phosphatase 2A (PP2A) holoenzyme.</Description>
-<Xref>PDB:2IAE</Xref>
-<Note>X-ray diffraction, 3.50 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Xing, Y.</Author>
-<Author>Li, Z.</Author>
-<Author>Chen, Y.</Author>
-<Author>Stock, J.B.</Author>
-<Author>Jeffrey, P.D.</Author>
-<Author>Shi, Y.</Author>
-</Authors>
-<Citation>Cell 133, 154-163, 2008</Citation>
-<Title>Structural mechanism of demethylation and inactivation of protein phosphatase 2A.</Title>
-<Xref>DOI:10.1016/j.cell.2008.02.041</Xref>
-<Xref>PMID:18394995</Xref>
-<Note>the modification of serine/threonine-protein phosphatase 2A catalytic subunit beta is required for protein phosphatase 2A (PP2A) activity, and is reversed by PP2A-specific methylesterase PME-1(EC 3.1.1.89)</Note>
-</ReferenceBlock>
-<Comment>The carboxy-terminal motif for this modification, [PAMV][DG]YFL*, is strongly conserved.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>[phosphatase 2A protein]-leucine-carboxy methyltransferase (EC 2.1.1.233)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>L</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Condition>incidental to RESID:AA0039</Condition>
-<Xref>GO:0018439</Xref>
-<Xref>PSI-MOD:00304</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>methylated carboxyl end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__leucine methyl ester__l">MOD_RES Leucine methyl ester</Feature>
-</Features>
-<Image src="/images/AA0299.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0299.PDB" />
-</Entry>
-<Entry id="AA0300">
-<Header>
-<Code>AA0300</Code>
-<Dates>
-<CreationDate>30-Jun-2001</CreationDate>
-<StrucRevDate>30-Jun-2001</StrucRevDate>
-<TextChngDate>31-Dec-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>hexakis-L-cysteinyl L-serinyl octairon heptasulfide</Name>
-<AlternateName>nitrogenase P-cluster</AlternateName>
-<Xref>COMe:BIM000067</Xref>
-<Xref>PDBHET:CLF</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 21 Fe 8 H 27 N 7 O 8 S 13</Formula>
-<FormalCharge>3-</FormalCharge>
-<Weight type="chemical">1369.03</Weight>
-<Weight type="physical">1368.310179</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005 AA0005 AA0005 AA0005 AA0005 AA0016">
-<Formula>C 0 Fe 8 H -8 N 0 O 0 S 7</Formula>
-<FormalCharge>3-</FormalCharge>
-<Weight type="chemical">663.12</Weight>
-<Weight type="physical">663.223042</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Peters, J.W.</Author>
-<Author>Stowell, M.H.</Author>
-<Author>Soltis, S.M.</Author>
-<Author>Finnegan, M.G.</Author>
-<Author>Johnson, M.K.</Author>
-<Author>Rees, D.C.</Author>
-</Authors>
-<Citation>Biochemistry 36, 1181-1187, 1997</Citation>
-<Title>Redox-dependent structural changes in the nitrogenase P-cluster.</Title>
-<Xref>DOI:10.1021/bi9626665</Xref>
-<Xref>PMID:9063865</Xref>
-<Note>structural reinterpretation</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mayer, S.M.</Author>
-<Author>Lawson, D.M.</Author>
-<Author>Gormal, C.A.</Author>
-<Author>Roe, S.M.</Author>
-<Author>Smith, B.E.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 292, 871-891, 1999</Citation>
-<Title>New insights into structure-function relationships in nitrogenase: A 1.6 Angstom resolution X-ray crystallographic study of Klebsiella pneumoniae MoFe-protein.</Title>
-<Xref>DOI:10.1006/jmbi.1999.3107</Xref>
-<Xref>PMID:10525412</Xref>
-<Note>X-ray diffraction, 1.6 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mayer, S.M.</Author>
-<Author>Lawson, D.M.</Author>
-<Author>Gormal, C.A.</Author>
-<Author>Roe, S.M.</Author>
-<Author>Smith, B.E.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, May 1999</Citation>
-<Description>Nitrogenase Mo-Fe protein from Klebsiella pneumoniae, dithionite-reduced state.</Description>
-<Xref>PDB:1QGU</Xref>
-<Note>X-ray diffraction, 1.6 angstroms, reduced form</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mayer, S.M.</Author>
-<Author>Lawson, D.M.</Author>
-<Author>Gormal, C.A.</Author>
-<Author>Roe, S.M.</Author>
-<Author>Smith, B.E.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, May 1999</Citation>
-<Description>Nitrogenase Mo-Fe protein from Klebsiella pneumoniae, phenosafranin oxidized state.</Description>
-<Xref>PDB:1QH1</Xref>
-<Note>X-ray diffraction, 1.6 angstroms, oxidized form</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Einsle, O.</Author>
-<Author>Tezcan, F.A.</Author>
-<Author>Andrade, S.L.A.</Author>
-<Author>Schmid, B.</Author>
-<Author>Yoshida, M.</Author>
-<Author>Howard, J.B.</Author>
-<Author>Rees, D.C.</Author>
-</Authors>
-<Citation>Science 297, 1696-1700, 2002</Citation>
-<Title>Nitrogenase MoFe-protein at 1.16 A resolution: a central ligand in the FeMo-cofactor.</Title>
-<Xref>DOI:10.1126/science.1073877</Xref>
-<Xref>PMID:12215645</Xref>
-<Note>X-ray diffraction, 1.16 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Einsle, O.</Author>
-<Author>Tezcan, F.A.</Author>
-<Author>Andrade, S.L.A.</Author>
-<Author>Schmid, B.</Author>
-<Author>Yoshida, M.</Author>
-<Author>Howard, J.B.</Author>
-<Author>Rees, D.C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, June 2002</Citation>
-<Description>Nitrogenase MoFe protein from Azotobacter vinelandii.</Description>
-<Xref>PDB:1M1N</Xref>
-<Note>X-ray diffraction, 1.16 angstroms</Note>
-</ReferenceBlock>
-<Comment>In the oxidized state the cluster can be described as two 4Fe-3S subclusters, one ligated by two cysteines, the other ligated by two cysteines and a serine, with the subclusters bridged by one mu-3 sulfur and two cysteine mu-2 sulfurs, one of these cysteines also being ligated through its alpha-amino group. In the reduced state, the serine and cysteine amino ligands are protonated and the bridging sulfur is mu-4 ligated.</Comment>
-<SequenceCode>
-<SequenceSpec>C, C, C, C, C, C, S</SequenceSpec>
-<Condition>cross-link 7</Condition>
-<Condition>incidental to RESID:AA0141</Condition>
-<Xref>GO:0018441</Xref>
-<Xref>PSI-MOD:00305</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>iron-sulfur protein</Keyword>
-<Keyword>metalloprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="metal__iron-sulfur (8fe-7s)__c">METAL Iron-sulfur (8Fe-7S)</Feature>
-</Features>
-<Image src="/images/AA0300.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0300.PDB" />
-</Entry>
-<Entry id="AA0301">
-<Header>
-<Code>AA0301</Code>
-<Dates>
-<CreationDate>24-Aug-2001</CreationDate>
-<StrucRevDate>24-Aug-2001</StrucRevDate>
-<TextChngDate>30-Apr-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-isoleucine or L-leucine</Name>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 11 N 1 O 1</Formula>
-<Weight type="chemical">113.16</Weight>
-<Weight type="physical">113.084064</Weight>
-</FormulaBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Dixon, H.B.F.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 264, 607-609, 1999</Citation>
-<Title>IUPAC-IUBMB Joint Commission on Biochemical Nomenclature (JCBN) and Nomenclature Committee of IUBMB (NC-IUBMB), newsletter 1999.</Title>
-<Xref>PMID:10523135</Xref>
-<Note>http://www.chem.qmul.ac.uk/iubmb/newsletter/1999/item3.html</Note>
-</ReferenceBlock>
-<Comment>This represents an uncertainty between L-isoleucine and L-leucine, sometimes encountered in mass spectrometry and NMR. The symbol and abbreviation have not officially been adopted by IUPAC or IUBMB.</Comment>
-<SequenceCode>
-<SequenceSpec>J</SequenceSpec>
-<Abbreviation>Xle</Abbreviation>
-<Xref>PSI-MOD:00306</Xref>
-</SequenceCode>
-<Source>ambiguity</Source>
-<Image src="/images/AA0301.GIF" alt="DUMMY.GIF" />
-</Entry>
-<Entry id="AA0302">
-<Header>
-<Code>AA0302</Code>
-<Dates>
-<CreationDate>24-Aug-2001</CreationDate>
-<StrucRevDate>24-Aug-2001</StrucRevDate>
-<TextChngDate>30-Jun-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-aspartimide</Name>
-<AlternateName>2-amino-butanimide</AlternateName>
-<AlternateName>alpha-aminosuccinimide</AlternateName>
-<AlternateName>ASI</AlternateName>
-<AlternateName>L-2-aminosuccinimide</AlternateName>
-<AlternateName>L-3-aminosuccinimide [misnomer]</AlternateName>
-<AlternateName>L-asparaginimide</AlternateName>
-<SystematicName>(3S)-3-amino-2,5-pyrrolidinedione</SystematicName>
-<Xref>CAS:5615-80-5</Xref>
-<Xref>PDBHET:SNN</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 5 N 2 O 2</Formula>
-<Weight type="chemical">113.10</Weight>
-<Weight type="physical">113.035102</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0003">
-<Formula>C 0 H -2 N 0 O -1</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Robson, V.M.</Author>
-<Author>Rae, I.D.</Author>
-<Author>Ng, F.</Author>
-</Authors>
-<Citation>Biol. Chem. Hoppe-Seyler 371, 423-431, 1990</Citation>
-<Title>Identification of the aspartimide structure in a previously-reported peptide.</Title>
-<Xref>PMID:2378679</Xref>
-<Note>report of modification not in an intein, probably artifactual</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Toney, K.</Author>
-<Author>Bateman, A.</Author>
-<Author>Gagnon, C.</Author>
-<Author>Bennett, H.P.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 268, 1024-1031, 1993</Citation>
-<Title>Aspartimide formation in the joining peptide sequence of porcine and mouse pro-opiomelanocortin.</Title>
-<Xref>PMID:8380403</Xref>
-<Note>mass spectrometric detection and enzymatic evidence for natural formation of aspartimide intermediate</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Xu, M.Q.</Author>
-<Author>Comb, D.G.</Author>
-<Author>Paulus, H.</Author>
-<Author>Noren, C.J.</Author>
-<Author>Shao, Y.</Author>
-<Author>Perler, F.B.</Author>
-</Authors>
-<Citation>EMBO J. 13, 5517-5522, 1994</Citation>
-<Title>Protein splicing: an analysis of the branched intermediate and its resolution by succinimide formation.</Title>
-<Xref>PMID:7988548</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Shao, Y.</Author>
-<Author>Xu, M.Q.</Author>
-<Author>Paulus, H.</Author>
-</Authors>
-<Citation>Biochemistry 34, 10844-10850, 1995</Citation>
-<Title>Protein splicing: characterization of the aminosuccinimide residue at the carboxyl terminus of the excised intervening sequence.</Title>
-<Xref>DOI:10.1021/bi00034a017</Xref>
-<Xref>PMID:7662664</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Shao, Y.</Author>
-<Author>Paulus, H.</Author>
-</Authors>
-<Citation>J. Pept. Res. 50, 193-198, 1997</Citation>
-<Title>Protein splicing: estimation of the rate of O-N and S-N acyl rearrangements, the last step of the splicing process.</Title>
-<Xref>PMID:9309583</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Regni, C.A.</Author>
-<Author>Roush, R.F.</Author>
-<Author>Miller, D.J.</Author>
-<Author>Nourse, A.</Author>
-<Author>Walsh, C.T.</Author>
-<Author>Schulman, B.A.</Author>
-</Authors>
-<Citation>EMBO J. 28, 1953-1964, 2009</Citation>
-<Title>How the MccB bacterial ancestor of ubiquitin E1 initiates biosynthesis of the microcin C7 antibiotic.</Title>
-<Xref>DOI:10.1038/emboj.2009.146</Xref>
-<Xref>PMID:19494832</Xref>
-<Note>this modification is produced as an intermediate by the MccB enzyme</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Regni, C.A.</Author>
-<Author>Roush, R.F.</Author>
-<Author>Miller, D.</Author>
-<Author>Nourse, A.</Author>
-<Author>Walsh, C.T.</Author>
-<Author>Schulman, B.A.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, April 2009</Citation>
-<Description>Crystal structure of E. coli MccB + succinimide.</Description>
-<Xref>PDB:3H5R</Xref>
-<Note>X-ray diffraction, 2.10 angstroms</Note>
-</ReferenceBlock>
-<Comment>This modification is autocatalytically produced from the carboxyl-terminal asparagine of spliced inteins.</Comment>
-<Comment>This modification is produced by the MccB enzyme as an intermediate in the process of biosynthesizing (3-aminopropyl)(L-aspartyl-1-amino)phosphoryl-5'-adenosine. See RESID:AA0328.</Comment>
-<SequenceCode>
-<SequenceSpec>N</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0019801</Xref>
-<Xref>PSI-MOD:00307</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>protein splicing</Keyword>
-<Keyword>succinimide ring</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0302.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0302.PDB" />
-</Entry>
-<Entry id="AA0303">
-<Header>
-<Code>AA0303</Code>
-<Dates>
-<CreationDate>24-Aug-2001</CreationDate>
-<StrucRevDate>24-Aug-2001</StrucRevDate>
-<TextChngDate>30-Jun-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-glutamimide</Name>
-<AlternateName>2-aminopentanimide</AlternateName>
-<AlternateName>3-amino-2,6-piperidinedione</AlternateName>
-<AlternateName>alpha-aminoglutarimide</AlternateName>
-<SystematicName>(3S)-3-aminopiperidine-2,6-dione</SystematicName>
-<Xref>CAS:2353-44-8</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 7 N 2 O 2</Formula>
-<Weight type="chemical">127.12</Weight>
-<Weight type="physical">127.050752</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0007">
-<Formula>C 0 H -2 N 0 O -1</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Amitai, G.</Author>
-<Author>Dassa, B.</Author>
-<Author>Pietrokovski, S.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 279, 3121-3131, 2004</Citation>
-<Title>Protein splicing of inteins with atypical glutamine and aspartate C-terminal residues.</Title>
-<Xref>DOI:10.1074/jbc.M311343200</Xref>
-<Xref>PMID:14593103</Xref>
-<Note>mass spectrometric identification</Note>
-</ReferenceBlock>
-<Comment>This modification is autocatalytically produced from the carboxyl-terminal glutamine of spliced inteins.</Comment>
-<SequenceCode>
-<SequenceSpec>Q</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0019802</Xref>
-<Xref>PSI-MOD:00308</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>protein splicing</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0303.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0303.PDB" />
-</Entry>
-<Entry id="AA0304">
-<Header>
-<Code>AA0304</Code>
-<Dates>
-<CreationDate>24-Aug-2001</CreationDate>
-<StrucRevDate>24-Aug-2001</StrucRevDate>
-<TextChngDate>30-Sep-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>3-carboxy-L-aspartic acid</Name>
-<AlternateName>2-amino-3-carboxybutanedioic acid</AlternateName>
-<AlternateName>3-carboxyaspartic acid</AlternateName>
-<AlternateName>beta-carboxyaspartic acid</AlternateName>
-<SystematicName>(2S)-2-aminoethane-1,1,2-tricarboxylic acid</SystematicName>
-<Xref>CAS:75898-26-9</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 5 N 1 O 5</Formula>
-<Weight type="chemical">159.10</Weight>
-<Weight type="physical">159.016772</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0004">
-<Formula>C 1 H 0 N 0 O 2</Formula>
-<Weight type="chemical">44.01</Weight>
-<Weight type="physical">43.989829</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hauschka, P.V.</Author>
-<Author>Henson, E.B.</Author>
-<Author>Gallop, P.M.</Author>
-</Authors>
-<Citation>Anal. Biochem. 108, 57-63, 1980</Citation>
-<Title>Quantitative analysis and comparative decarboxylation of aminomalonic acid, beta-carboxyaspartic acid, and gamma-carboxyglutamic acid.</Title>
-<Xref>DOI:10.1016/0003-2697(80)90691-0</Xref>
-<Xref>PMID:7457858</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Richey, B.</Author>
-<Author>Christy, M.R.</Author>
-<Author>Haltiwanger, R.C.</Author>
-<Author>Koch, T.H.</Author>
-<Author>Gill, S.J.</Author>
-</Authors>
-<Citation>Biochemistry 21, 4819-4823, 1982</Citation>
-<Title>Unusual zwitterion of D,L-beta-carboxyaspartic acid: pKa and X-ray crystallographic measurements.</Title>
-<Xref>DOI:10.1021/bi00262a046</Xref>
-<Xref>PMID:7138832</Xref>
-<Note>X-ray diffraction; pKa determinations</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Koch, T.H.</Author>
-<Author>Christy, M.R.</Author>
-<Author>Barkley, R.M.</Author>
-<Author>Sluski, R.</Author>
-<Author>Bohemier, D.</Author>
-<Author>Van Buskirk, J.J.</Author>
-<Author>Kirsch, W.M.</Author>
-</Authors>
-<Citation>Meth. Enzymol. 107, 563-575, 1984</Citation>
-<Title>beta-Carboxyaspartic acid.</Title>
-<Xref>DOI:10.1016/0076-6879(84)07040-3</Xref>
-<Xref>PMID:6390094</Xref>
-<Note>review</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Nishimoto, S.K.</Author>
-<Author>Zhao, J.</Author>
-<Author>Dass, C.</Author>
-</Authors>
-<Citation>Anal. Biochem. 216, 159-164, 1994</Citation>
-<Title>Isolation and characterization of the reaction product of 4-diazobenzenesulfonic acid and gamma-carboxyglutamic acid: modification of the assay for measurement of beta-carboxyaspartic acid.</Title>
-<Xref>DOI:10.1006/abio.1994.1020</Xref>
-<Xref>PMID:8135347</Xref>
-<Note>colorimetric detection</Note>
-</ReferenceBlock>
-<Comment>This extremely acid labile modification has been detected but not located by sequencing in proteins.</Comment>
-<SequenceCode>
-<SequenceSpec>D</SequenceSpec>
-<Xref>GO:0019803</Xref>
-<Xref>PSI-MOD:00309</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0304.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0304.PDB" />
-</Entry>
-<Entry id="AA0305">
-<Header>
-<Code>AA0305</Code>
-<Dates>
-<CreationDate>24-Aug-2001</CreationDate>
-<StrucRevDate>24-Aug-2001</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N5-methyl-L-arginine</Name>
-<AlternateName>delta-N-methylarginine</AlternateName>
-<AlternateName>N5-carbamimidoyl-N5-methyl-L-ornithine</AlternateName>
-<SystematicName>(2S)-2-amino-5-(N-methylcarbamimidamido)pentanoic acid</SystematicName>
-<Xref>ChEBI:21848</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 14 N 4 O 1</Formula>
-<Weight type="chemical">170.22</Weight>
-<Weight type="physical">170.116761</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0002">
-<Formula>C 1 H 2 N 0 O 0</Formula>
-<Weight type="chemical">14.03</Weight>
-<Weight type="physical">14.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Zobel-Thropp, P.</Author>
-<Author>Gary, J.D.</Author>
-<Author>Clarke, S.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 273, 29283-29286, 1998</Citation>
-<Title>delta-N-methylarginine is a novel posttranslational modification of arginine residues in yeast proteins.</Title>
-<Xref>DOI:10.1074/jbc.273.45.29283</Xref>
-<Xref>PMID:9792625</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Niewmierzycka, A.</Author>
-<Author>Clarke, S.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 274, 814-824, 1999</Citation>
-<Title>S-Adenosylmethionine-dependent methylation in Saccharomyces cerevisiae. Identification of a novel protein arginine methyltransferase.</Title>
-<Xref>DOI:10.1074/jbc.274.2.814</Xref>
-<Xref>PMID:9873020</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Chern, M.K.</Author>
-<Author>Chang, K.N.</Author>
-<Author>Liu, L.F.</Author>
-<Author>Tam, T.C.</Author>
-<Author>Liu, Y.C.</Author>
-<Author>Liang, Y.L.</Author>
-<Author>Tam, M.F.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 277, 15345-15353, 2002</Citation>
-<Title>Yeast ribosomal protein L12 is a substrate of protein-arginine methyltransferase 2.</Title>
-<Xref>DOI:10.1074/jbc.M111379200</Xref>
-<Xref>PMID:11856739</Xref>
-</ReferenceBlock>
-<Comment>This modification should not be confused with 5-methylarginine (see RESID:AA0272).</Comment>
-<GeneratingEnzyme>
-<EnzymeName>protein-arginine N5-methyltransferase (EC 2.1.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>R</SequenceSpec>
-<Xref>GO:0019701</Xref>
-<Xref>PSI-MOD:00310</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>methylated amino acid</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n5-methylarginine__r">MOD_RES N5-methylarginine</Feature>
-</Features>
-<Image src="/images/AA0305.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0305.PDB" />
-</Entry>
-<Entry id="AA0306">
-<Header>
-<Code>AA0306</Code>
-<Dates>
-<CreationDate>24-Aug-2001</CreationDate>
-<StrucRevDate>24-Aug-2001</StrucRevDate>
-<TextChngDate>30-Sep-2008</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-cysteine coenzyme A disulfide</Name>
-<AlternateName>coenzyme A L-cysteine mixed disulfide</AlternateName>
-<SystematicName>(2R)-2-amino-3-(2-((3-(((2R)-2,4-dihydroxy-3,3-dimethyl-1-oxobutyl)amino)-1-oxopropyl)amino)ethyl)dithio-propanoic acid 4'-ester with adenosine 5'-(trihydrogen diphosphate) 3'-(dihydrogen phosphate)</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 24 H 39 N 8 O 17 P 3 S 2</Formula>
-<Weight type="chemical">868.66</Weight>
-<Weight type="physical">868.108744</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 21 H 34 N 7 O 16 P 3 S 1</Formula>
-<Weight type="chemical">765.52</Weight>
-<Weight type="physical">765.099559</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Thorneley, R.N.</Author>
-<Author>Abell, C.</Author>
-<Author>Ashby, G.A.</Author>
-<Author>Drummond, M.H.</Author>
-<Author>Eady, R.R.</Author>
-<Author>Huff, S.</Author>
-<Author>Macdonald, C.J.</Author>
-<Author>Shneier, A.</Author>
-</Authors>
-<Citation>Biochemistry 31, 1216-1224, 1992</Citation>
-<Title>Posttranslational modification of Klebsiella pneumoniae flavodoxin by covalent attachment of coenzyme A, shown by 31P NMR and electrospray mass spectrometry, prevents electron transfer from the nifJ protein to nitrogenase. A possible new regulatory mechanism for biological nitrogen fixation.</Title>
-<Xref>DOI:10.1021/bi00119a035</Xref>
-<Xref>PMID:1734967</Xref>
-<Note>this modification, of a Klebsiella pneumoniae protein over-expressed in Escherichia coli cells, has not been demonstrated under natural conditions</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>GO:0019703</Xref>
-<Xref>PSI-MOD:00311</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>coenzyme A</Keyword>
-<Keyword>disulfide bond</Keyword>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0306.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0306.PDB" />
-</Entry>
-<Entry id="AA0307">
-<Header>
-<Code>AA0307</Code>
-<Dates>
-<CreationDate>07-Sep-2001</CreationDate>
-<StrucRevDate>07-Sep-2001</StrucRevDate>
-<TextChngDate>01-Mar-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-myristoyl-L-cysteine</Name>
-<AlternateName>tetradecanoate cysteine thioester</AlternateName>
-<SystematicName>(R)-2-amino-3-(tetradecanoylsulfanyl)propanoic acid</SystematicName>
-<Xref>ChEBI:22061</Xref>
-<Xref>PDBHET:MYR</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 17 H 31 N 1 O 2 S 1</Formula>
-<Weight type="chemical">313.50</Weight>
-<Weight type="physical">313.207550</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 14 H 26 N 0 O 1 S 0</Formula>
-<Weight type="chemical">210.36</Weight>
-<Weight type="physical">210.198365</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Armah, D.A.</Author>
-<Author>Mensa-Wilmot, K.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 274, 5931-5938, 1999</Citation>
-<Title>S-Myristoylation of a glycosylphosphatidylinositol-specific phospholipase C in Trypanosoma brucei.</Title>
-<Xref>DOI:10.1074/jbc.274.9.5931</Xref>
-<Xref>PMID:10026218</Xref>
-<Note>chemical characterization; chromatographic detection; radioisotope labeling</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Armah, D.A.</Author>
-<Author>Mensa-Wilmot, K.</Author>
-</Authors>
-<Citation>Biochem. Biophys. Res. Commun. 256, 569-572, 1999</Citation>
-<Title>Protein S-myristoylation in Leishmania revealed with a heterologous reporter.</Title>
-<Xref>DOI:10.1006/bbrc.1999.0376</Xref>
-<Xref>PMID:10080938</Xref>
-<Note>chemical characterization; chromatographic detection; radioisotope labeling</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Steinert, P.M.</Author>
-<Author>Kim, S.Y.</Author>
-<Author>Chung, S.I.</Author>
-<Author>Marekov, L.N.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 271, 26242-26250, 1996</Citation>
-<Title>The transglutaminase 1 enzyme is variably acylated by myristate and palmitate during differentiation in epidermal keratinocytes.</Title>
-<Xref>DOI:10.1074/jbc.271.42.26242</Xref>
-<Xref>PMID:8824274</Xref>
-<Note>mass spectrometric identification; differential S-palmitoylation and S-myristoylation (see RESID:AA0106)</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kim, Y.G.</Author>
-<Author>Sohn, E.J.</Author>
-<Author>Seo, J.</Author>
-<Author>Lee, K.J.</Author>
-<Author>Lee, H.S.</Author>
-<Author>Hwang, I.</Author>
-<Author>Whiteway, M.</Author>
-<Author>Sacher, M.</Author>
-<Author>Oh, B.H.</Author>
-</Authors>
-<Citation>Nature Struct. Mol. Biol. 12, 38-45, 2005</Citation>
-<Title>Crystal structure of bet3 reveals a novel mechanism for Golgi localization of tethering factor TRAPP.</Title>
-<Xref>DOI:10.1038/nsmb871</Xref>
-<Xref>PMID:15608655</Xref>
-<Note>X-ray diffraction, 1.60 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kim, Y.-G.</Author>
-<Author>Sacher, M.</Author>
-<Author>Oh, B.-H.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, November 2004</Citation>
-<Description>The Crystal Structure of Truncated Mouse Bet3P.</Description>
-<Xref>PDB:1WC9</Xref>
-<Note>X-ray diffraction, 1.60 angstroms</Note>
-</ReferenceBlock>
-<Comment>The predominant palmitoyl transferase in mammalian systems appears to utilize a mixture of saturated and unsaturated fatty acids including myristoic acid. Some systems may be more specific in their incorporation of other fatty acids. See RESID:AA0106 and RESID:AA0308.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>protein-cysteine S-myristoyltransferase (EC 2.3.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>GO:0019704</Xref>
-<Xref>GO:0042050</Xref>
-<Xref>PSI-MOD:00312</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lipoprotein</Keyword>
-<Keyword>myristoylation</Keyword>
-<Keyword>thioester bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__s-myristoyl cysteine__c">LIPID S-myristoyl cysteine</Feature>
-</Features>
-<Image src="/images/AA0307.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0307.PDB" />
-</Entry>
-<Entry id="AA0308">
-<Header>
-<Code>AA0308</Code>
-<Dates>
-<CreationDate>07-Sep-2001</CreationDate>
-<StrucRevDate>07-Sep-2001</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-palmitoleoyl-L-cysteine</Name>
-<AlternateName>cis-9-hexadecenoate cysteine thioester</AlternateName>
-<AlternateName>S-palmitoleyl-L-cysteine [misnomer]</AlternateName>
-<SystematicName>(R)-2-amino-3-((Z)-9-hexadecenoylsulfanyl)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 19 H 33 N 1 O 2 S 1</Formula>
-<Weight type="chemical">339.54</Weight>
-<Weight type="physical">339.223200</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 16 H 28 N 0 O 1 S 0</Formula>
-<Weight type="chemical">236.40</Weight>
-<Weight type="physical">236.214016</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Casey, W.M.</Author>
-<Author>Gibson, K.J.</Author>
-<Author>Parks, L.W.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 269, 2082-2085, 1994</Citation>
-<Title>Covalent attachment of palmitoleic acid (C16:1 Delta 9) to proteins in Saccharomyces cerevisiae. Evidence for a third class of acylated proteins.</Title>
-<Xref>PMID:8294460</Xref>
-</ReferenceBlock>
-<Comment>This specific modification has been detected but not located by sequencing in proteins. This modification may also arise from non-specific activity of the enzymes that produce S-palmitoyl-L-cysteine; see RESID:AA0106.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>protein-cysteine S-palmitoleoyltransferase (EC 2.3.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>GO:0019939</Xref>
-<Xref>GO:0042050</Xref>
-<Xref>PSI-MOD:00313</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>lipoprotein</Keyword>
-<Keyword>thioester bond</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0308.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0308.PDB" />
-</Entry>
-<Entry id="AA0309">
-<Header>
-<Code>AA0309</Code>
-<Dates>
-<CreationDate>07-Sep-2001</CreationDate>
-<StrucRevDate>07-Sep-2001</StrucRevDate>
-<TextChngDate>29-Nov-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>glycine cholesterol ester</Name>
-<AlternateName>cholesteryl glycinate</AlternateName>
-<AlternateName>hedgehog lipophilic adduct</AlternateName>
-<SystematicName>glycine cholest-5-en-3beta-ol ester</SystematicName>
-<Xref>CAS:57-88-5</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 29 H 48 N 1 O 2</Formula>
-<Weight type="chemical">442.71</Weight>
-<Weight type="physical">442.368505</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0008">
-<Formula>C 27 H 44 N 0 O 0</Formula>
-<Weight type="chemical">368.65</Weight>
-<Weight type="physical">368.344301</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Porter, J.A.</Author>
-<Author>Young, K.E.</Author>
-<Author>Beachy, P.A.</Author>
-</Authors>
-<Citation>Science 274, 255-259, 1996</Citation>
-<Title>Cholesterol modification of hedgehog signaling proteins in animal development.</Title>
-<Xref>DOI:10.1126/science.274.5285.255</Xref>
-<Xref>PMID:8824192</Xref>
-<Note>chemical characterization; chromatographic detection; radioisotope labeling</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mann, R.K.</Author>
-<Author>Beachy, P.A.</Author>
-</Authors>
-<Citation>Biochim. Biophys. Acta 1529, 188-202, 2000</Citation>
-<Title>Cholesterol modification of proteins.</Title>
-<Xref>DOI:10.1016/S1388-1981(00)00148-7</Xref>
-<Xref>PMID:11111088</Xref>
-<Note>review article</Note>
-</ReferenceBlock>
-<Comment>This modification occurs at the carboxyl end released during autolytic cleavage.</Comment>
-<SequenceCode>
-<SequenceSpec>G</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Condition>incidental to RESID:AA0060</Condition>
-<Xref>GO:0019708</Xref>
-<Xref>PSI-MOD:00314</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>lipoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__cholesterol glycine ester__g">LIPID Cholesterol glycine ester</Feature>
-</Features>
-<Image src="/images/AA0309.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0309.PDB" />
-</Entry>
-<Entry id="AA0310">
-<Header>
-<Code>AA0310</Code>
-<Dates>
-<CreationDate>30-Sep-2001</CreationDate>
-<StrucRevDate>30-Sep-2001</StrucRevDate>
-<TextChngDate>31-Dec-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>pentakis-L-cysteinyl L-histidino nickel tetrairon pentasulfide</Name>
-<AlternateName>carbon monoxide dehydrogenase nickel-iron cofactor</AlternateName>
-<AlternateName>Ni-4Fe-5S cluster</AlternateName>
-<SystematicName>mu-1:2kappaS-sulfido-mu3-1:3:5kappaS-sulfido-mu3-2:3:4kappaS-sulfido-mu3-2:4:5kappaS-sulfido-mu3-3:4:5kappaS-sulfido-N1'-histidino-S-cysteinyl-1-iron-S-cysteinyl-2-nickel-3,4,5-tris-(S-cysteinyl iron)</SystematicName>
-<Xref>COMe:BIM000272</Xref>
-<Xref>PDBHET:NFS</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 21 Fe 4 H 26 N 8 Ni 1 O 6 S 10</Formula>
-<Weight type="chemical">1089.16</Weight>
-<Weight type="physical">1087.593333</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005 AA0005 AA0005 AA0005 AA0009">
-<Formula>C 0 Fe 4 H -6 N 0 Ni 1 O 0 S 5</Formula>
-<Weight type="chemical">436.33</Weight>
-<Weight type="physical">435.488498</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Stephens, P.J.</Author>
-<Author>McKenna, M.C.</Author>
-<Author>Ensign, S.A.</Author>
-<Author>Bonam, D.</Author>
-<Author>Ludden, P.W.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 264, 16347-16350, 1989</Citation>
-<Title>Identification of a Ni- and Fe-containing cluster in Rhodospirillum rubrum carbon monoxide dehydrogenase.</Title>
-<Xref>PMID:2550436</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Dobbek, H.</Author>
-<Author>Svetlitchnyi, V.</Author>
-<Author>Gremer, L.</Author>
-<Author>Huber, R.</Author>
-<Author>Meyer, O.</Author>
-</Authors>
-<Citation>Science 293, 1281-1285, 2001</Citation>
-<Title>Crystal structure of a carbon monoxide dehydrogenase reveals a [Ni-4Fe-5S] cluster.</Title>
-<Xref>DOI:10.1126/science.1061500</Xref>
-<Xref>PMID:11509720</Xref>
-<Note>X-ray diffraction, 1.6 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Dobbek, H.</Author>
-<Author>Svetlitchnyi, V.</Author>
-<Author>Liss, J.</Author>
-<Author>Meyer, O.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 126, 5382-5387, 2004</Citation>
-<Title>Carbon monoxide induced decomposition of the active site [Ni-4Fe-5S] cluster of CO dehydrogenase.</Title>
-<Xref>DOI:10.1021/ja037776v</Xref>
-<Xref>PMID:15113209</Xref>
-<Note>X-ray diffraction, 1.12 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Dobbek, H.</Author>
-<Author>Svetlitchnyi, V.</Author>
-<Author>Gremer, L.</Author>
-<Author>Huber, R.</Author>
-<Author>Meyer, O.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, May 2004</Citation>
-<Description>Carbon monoxide dehydrogenase from Carboxydothermus hydrogenoformans - DTT reduced state.</Description>
-<Xref>PDB:1SU7</Xref>
-<Note>X-ray diffraction, 1.12 angstroms</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>C, C, C, C, C, H</SequenceSpec>
-<Condition>cross-link 6</Condition>
-<Xref>GO:0019709</Xref>
-<Xref>GO:0042075</Xref>
-<Xref>PSI-MOD:00315</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>iron-sulfur protein</Keyword>
-<Keyword>metalloprotein</Keyword>
-<Keyword>Ni-4Fe-5S</Keyword>
-<Keyword>nickel</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="metal__nickel-iron-sulfur (ni-4fe-5s)__c">METAL Nickel-iron-sulfur (Ni-4Fe-5S)</Feature>
-<Feature type="UniProt" key="metal__nickel-iron-sulfur (ni-4fe-5s); via tele nitrogen__h">METAL Nickel-iron-sulfur (Ni-4Fe-5S); via tele nitrogen</Feature>
-</Features>
-<Image src="/images/AA0310.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0310.PDB" />
-</Entry>
-<Entry id="AA0311">
-<Header>
-<Code>AA0311</Code>
-<Dates>
-<CreationDate>30-Sep-2001</CreationDate>
-<StrucRevDate>30-Sep-2001</StrucRevDate>
-<TextChngDate>30-Sep-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N4,N4-dimethyl-L-asparagine</Name>
-<AlternateName>2-amino-N4,N4-dimethylbutanediamic acid</AlternateName>
-<AlternateName>beta-dimethylasparagine [misnomer]</AlternateName>
-<AlternateName>N(gamma),N(gamma)-dimethylasparagine</AlternateName>
-<SystematicName>(2S)-2-amino-4-(dimethylamino)-4-oxobutanoic acid</SystematicName>
-<Xref>PDBHET:DMH</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 10 N 2 O 2</Formula>
-<Weight type="chemical">142.16</Weight>
-<Weight type="physical">142.074228</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0003">
-<Formula>C 2 H 4 N 0 O 0</Formula>
-<Weight type="chemical">28.05</Weight>
-<Weight type="physical">28.031300</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ducret, A.</Author>
-<Author>Bruun, C.F.</Author>
-<Author>Bures, E.J.</Author>
-<Author>Marhaug, G.</Author>
-<Author>Husby, G.</Author>
-<Author>Aebersold, R.</Author>
-</Authors>
-<Citation>Electrophoresis 17, 866-876, 1996</Citation>
-<Title>Characterization of human serum amyloid A protein isoforms separated by two-dimensional electrophoresis by liquid chromatography/electrospray ionization tandem mass spectrometry.</Title>
-<Xref>DOI:10.1002/elps.1150170508</Xref>
-<Xref>PMID:8783012</Xref>
-<Note>mass spectrometric detection</Note>
-</ReferenceBlock>
-<Comment>This structure has not been confirmed.</Comment>
-<SequenceCode>
-<SequenceSpec>N</SequenceSpec>
-<Xref>GO:0019710</Xref>
-<Xref>PSI-MOD:00316</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>methylated amino acid</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n4,n4-dimethylasparagine__n">MOD_RES N4,N4-dimethylasparagine</Feature>
-</Features>
-<Image src="/images/AA0311.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0311.PDB" />
-</Entry>
-<Entry id="AA0312">
-<Header>
-<Code>AA0312</Code>
-<Dates>
-<CreationDate>31-Dec-2001</CreationDate>
-<StrucRevDate>31-Dec-2001</StrucRevDate>
-<TextChngDate>13-Sep-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6-(3,4-didehydroretinylidene)-L-lysine</Name>
-<AlternateName>N6-3-dehydroretinal-L-lysine</AlternateName>
-<AlternateName>N6-3-dehydroretinyl-lysine</AlternateName>
-<SystematicName>(S)-2-amino-6-[(2E,4E,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethylcyclohexa-1,3-dien-1-yl)-2,4,6,8-nonatetraenylidene]aminohexanoic acid</SystematicName>
-<Xref>CAS:472-87-7</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 26 H 36 N 2 O 1</Formula>
-<Weight type="chemical">392.59</Weight>
-<Weight type="physical">392.282764</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 20 H 24 N 0 O 0</Formula>
-<Weight type="chemical">264.41</Weight>
-<Weight type="physical">264.187801</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Suzuki, T.</Author>
-<Author>Maeda, Y.</Author>
-<Author>Toh, Y.</Author>
-<Author>Eguchi, E.</Author>
-</Authors>
-<Citation>Vision Res. 28, 1061-1070, 1988</Citation>
-<Title>Retinyl and 3-dehydroretinyl esters in the crayfish retina.</Title>
-<Xref>DOI:10.1016/0042-6989(88)90132-0</Xref>
-<Xref>PMID:3257009</Xref>
-<Note>identification of covalently bound 3-dehydroretinal as the visual pigment in a porphyropsin</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Tsin, A.T.</Author>
-<Author>Santos, F.R.</Author>
-</Authors>
-<Citation>J. Exp. Zool. 235, 181-186, 1985</Citation>
-<Title>The 3,4-didehydroretinal chromophore of goldfish porphyropsin.</Title>
-<Xref>DOI:10.1002/jez.1402350204</Xref>
-<Xref>PMID:4056688</Xref>
-<Note>interconversion of the all-trans and 11-cis forms in a porphyropsin</Note>
-</ReferenceBlock>
-<Comment>The all-trans form is shown. Light-induced interconversion with the 11-cis (4Z) form in porphyropsin and cyanopsin is utilized for light sensing in some animals.</Comment>
-<Comment>This modification has been detected but not located by sequencing in proteins. It may be substituted for retinal (see RESID:AA0120) in opsin.</Comment>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>GO:0019931</Xref>
-<Xref>PSI-MOD:00317</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chromoprotein</Keyword>
-<Keyword>retinal</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0312.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0312.PDB" />
-</Entry>
-<Entry id="AA0313">
-<Header>
-<Code>AA0313</Code>
-<Dates>
-<CreationDate>31-Dec-2001</CreationDate>
-<StrucRevDate>31-Dec-2001</StrucRevDate>
-<TextChngDate>24-Aug-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>4'-(L-cystein-S-yl)-L-tryptophyl quinone</Name>
-<AlternateName>3-(2-amino-2-carboxyethyl)-4-[2-amino-2-carboxyethyl]sulfanyl-6,7-indolinedione</AlternateName>
-<AlternateName>4-(S-cysteinyl)tryptophan-6,7-dione</AlternateName>
-<AlternateName>CTQ</AlternateName>
-<AlternateName>cysteine tryptophylquinone</AlternateName>
-<SystematicName>(2R)-2-amino-3-[(3-[(2S)-2-amino-2-carboxyethyl]-6,7-dioxo-6,7-dihydro-1H-indol-4-yl)sulfanyl]propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 14 H 11 N 3 O 4 S 1</Formula>
-<Weight type="chemical">317.32</Weight>
-<Weight type="physical">317.047027</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0018">
-<Formula>C 0 H -4 N 0 O 2 S 0</Formula>
-<Weight type="chemical">27.97</Weight>
-<Weight type="physical">27.958529</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Datta, S.</Author>
-<Author>Mori, Y.</Author>
-<Author>Takagi, K.</Author>
-<Author>Kawaguchi, K.</Author>
-<Author>Chen, Z.W.</Author>
-<Author>Okajima, T.</Author>
-<Author>Kuroda, S.</Author>
-<Author>Ikeda, T.</Author>
-<Author>Kano, K.</Author>
-<Author>Tanizawa, K.</Author>
-<Author>Mathews, F.S.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 98, 14268-14273, 2001</Citation>
-<Title>Structure of a quinohemoprotein amine dehydrogenase with an uncommon redox cofactor and highly unusual crosslinking.</Title>
-<Xref>DOI:10.1073/pnas.241429098</Xref>
-<Xref>PMID:11717396</Xref>
-<Note>X-ray diffraction, 2.05 angstroms; mass spectrometric characterization; p-nitrophenylhydrazine derivative of cysteine tryptophylquinone</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Datta, S.</Author>
-<Author>Mori, Y.</Author>
-<Author>Takagi, K.</Author>
-<Author>Kawaguchi, K.</Author>
-<Author>Chen, Z.W.</Author>
-<Author>Kano, K.</Author>
-<Author>Ikeda, T.</Author>
-<Author>Okajima, T.</Author>
-<Author>Kuroda, S.</Author>
-<Author>Tanizawa, K.</Author>
-<Author>Mathews, F.S.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, July 2001</Citation>
-<Description>Structure of a quinohemoprotein amine dehydrogenase with a unique redox cofactor and highly unusual crosslinking.</Description>
-<Xref>PDB:1JJU</Xref>
-<Note>X-ray diffraction, 2.05 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Vandenberghe, I.</Author>
-<Author>Kim, J.K.</Author>
-<Author>Devreese, B.</Author>
-<Author>Hacisalihoglu, A.</Author>
-<Author>Iwabuki, H.</Author>
-<Author>Okajima, T.</Author>
-<Author>Kuroda, S.</Author>
-<Author>Adachi, O.</Author>
-<Author>Jongejan, J.A.</Author>
-<Author>Duine, J.A.</Author>
-<Author>Tanizawa, K.</Author>
-<Author>Van Beeumen, J.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 276, 42923-42931, 2001</Citation>
-<Title>The covalent structure of the small subunit from Pseudomonas putida amine dehydrogenase reveals the presence of three novel types of internal cross-linkages, all involving cysteine in a thioether bond.</Title>
-<Xref>DOI:10.1074/jbc.M107164200</Xref>
-<Xref>PMID:11555656</Xref>
-<Note>mass spectrometric and chemical characterization</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>C, W</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Condition>secondary to RESID:AA0148</Condition>
-<Xref>GO:0019927</Xref>
-<Xref>PSI-MOD:00318</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>quinoprotein</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__4&apos;-cysteinyl-tryptophylquinone (cys-trp)__c__w">CROSSLNK 4'-cysteinyl-tryptophylquinone (Cys-Trp)</Feature>
-</Features>
-<Image src="/images/AA0313.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0313.PDB" />
-</Entry>
-<Entry id="AA0314">
-<Header>
-<Code>AA0314</Code>
-<Dates>
-<CreationDate>31-Dec-2001</CreationDate>
-<StrucRevDate>31-Dec-2001</StrucRevDate>
-<TextChngDate>31-Mar-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>3-(L-cystein-S-yl)-L-aspartic acid</Name>
-<AlternateName>(2R,3S,6R)-2,6-diamino-3-carboxy-4-thiaheptanedioic acid</AlternateName>
-<AlternateName>3-carboxy-L-lanthionine</AlternateName>
-<SystematicName>(2R,3S)-2-amino-3-([(2R)-2-amino-2-carboxyethyl]sulfanyl)butanedioic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 8 N 2 O 4 S 1</Formula>
-<Weight type="chemical">216.21</Weight>
-<Weight type="physical">216.020478</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0004 AA0005">
-<Formula>C 0 H -2 N 0 O 0 S 0</Formula>
-<Weight type="chemical">-2.02</Weight>
-<Weight type="physical">-2.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Datta, S.</Author>
-<Author>Mori, Y.</Author>
-<Author>Takagi, K.</Author>
-<Author>Kawaguchi, K.</Author>
-<Author>Chen, Z.W.</Author>
-<Author>Okajima, T.</Author>
-<Author>Kuroda, S.</Author>
-<Author>Ikeda, T.</Author>
-<Author>Kano, K.</Author>
-<Author>Tanizawa, K.</Author>
-<Author>Mathews, F.S.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 98, 14268-14273, 2001</Citation>
-<Title>Structure of a quinohemoprotein amine dehydrogenase with an uncommon redox cofactor and highly unusual crosslinking.</Title>
-<Xref>DOI:10.1073/pnas.241429098</Xref>
-<Xref>PMID:11717396</Xref>
-<Note>X-ray diffraction, 2.05 angstroms; mass spectrometric characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Datta, S.</Author>
-<Author>Mori, Y.</Author>
-<Author>Takagi, K.</Author>
-<Author>Kawaguchi, K.</Author>
-<Author>Chen, Z.W.</Author>
-<Author>Kano, K.</Author>
-<Author>Ikeda, T.</Author>
-<Author>Okajima, T.</Author>
-<Author>Kuroda, S.</Author>
-<Author>Tanizawa, K.</Author>
-<Author>Mathews, F.S.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, July 2001</Citation>
-<Description>Structure of a quinohemoprotein amine dehydrogenase with a unique redox cofactor and highly unusual crosslinking.</Description>
-<Xref>PDB:1JJU</Xref>
-<Note>X-ray diffraction, 2.05 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Vandenberghe, I.</Author>
-<Author>Kim, J.K.</Author>
-<Author>Devreese, B.</Author>
-<Author>Hacisalihoglu, A.</Author>
-<Author>Iwabuki, H.</Author>
-<Author>Okajima, T.</Author>
-<Author>Kuroda, S.</Author>
-<Author>Adachi, O.</Author>
-<Author>Jongejan, J.A.</Author>
-<Author>Duine, J.A.</Author>
-<Author>Tanizawa, K.</Author>
-<Author>Van Beeumen, J.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 276, 42923-42931, 2001</Citation>
-<Title>The covalent structure of the small subunit from Pseudomonas putida amine dehydrogenase reveals the presence of three novel types of internal cross-linkages, all involving cysteine in a thioether bond.</Title>
-<Xref>DOI:10.1074/jbc.M107164200</Xref>
-<Xref>PMID:11555656</Xref>
-<Note>mass spectrometric and chemical characterization</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>C, D</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>GO:0019928</Xref>
-<Xref>PSI-MOD:00319</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lanthionine</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__3-cysteinyl-aspartic acid (cys-asp)__c__d">CROSSLNK 3-cysteinyl-aspartic acid (Cys-Asp)</Feature>
-</Features>
-<Image src="/images/AA0314.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0314.PDB" />
-</Entry>
-<Entry id="AA0315">
-<Header>
-<Code>AA0315</Code>
-<Dates>
-<CreationDate>31-Dec-2001</CreationDate>
-<StrucRevDate>31-Dec-2001</StrucRevDate>
-<TextChngDate>31-Mar-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>4-(L-cystein-S-yl)-L-glutamic acid</Name>
-<AlternateName>(2S,3S,7R)-2,7-diamino-4-carboxy-5-thiaoctanedioic acid</AlternateName>
-<SystematicName>(2S,4S)-2-amino-4-[(R)-2-amino-2-carboxyethyl]sulfanylpentanedioic acid</SystematicName>
-<Xref>ChEBI:20293</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 8 H 10 N 2 O 4 S 1</Formula>
-<Weight type="chemical">230.24</Weight>
-<Weight type="physical">230.036128</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0006">
-<Formula>C 0 H -2 N 0 O 0 S 0</Formula>
-<Weight type="chemical">-2.02</Weight>
-<Weight type="physical">-2.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Datta, S.</Author>
-<Author>Mori, Y.</Author>
-<Author>Takagi, K.</Author>
-<Author>Kawaguchi, K.</Author>
-<Author>Chen, Z.W.</Author>
-<Author>Okajima, T.</Author>
-<Author>Kuroda, S.</Author>
-<Author>Ikeda, T.</Author>
-<Author>Kano, K.</Author>
-<Author>Tanizawa, K.</Author>
-<Author>Mathews, F.S.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 98, 14268-14273, 2001</Citation>
-<Title>Structure of a quinohemoprotein amine dehydrogenase with an uncommon redox cofactor and highly unusual crosslinking.</Title>
-<Xref>DOI:10.1073/pnas.241429098</Xref>
-<Xref>PMID:11717396</Xref>
-<Note>X-ray diffraction, 2.05 angstroms; mass spectrometric characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Datta, S.</Author>
-<Author>Mori, Y.</Author>
-<Author>Takagi, K.</Author>
-<Author>Kawaguchi, K.</Author>
-<Author>Chen, Z.W.</Author>
-<Author>Kano, K.</Author>
-<Author>Ikeda, T.</Author>
-<Author>Okajima, T.</Author>
-<Author>Kuroda, S.</Author>
-<Author>Tanizawa, K.</Author>
-<Author>Mathews, F.S.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, July 2001</Citation>
-<Description>Structure of a quinohemoprotein amine dehydrogenase with a unique redox cofactor and highly unusual crosslinking.</Description>
-<Xref>PDB:1JJU</Xref>
-<Note>X-ray diffraction, 2.05 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Vandenberghe, I.</Author>
-<Author>Kim, J.K.</Author>
-<Author>Devreese, B.</Author>
-<Author>Hacisalihoglu, A.</Author>
-<Author>Iwabuki, H.</Author>
-<Author>Okajima, T.</Author>
-<Author>Kuroda, S.</Author>
-<Author>Adachi, O.</Author>
-<Author>Jongejan, J.A.</Author>
-<Author>Duine, J.A.</Author>
-<Author>Tanizawa, K.</Author>
-<Author>Van Beeumen, J.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 276, 42923-42931, 2001</Citation>
-<Title>The covalent structure of the small subunit from Pseudomonas putida amine dehydrogenase reveals the presence of three novel types of internal cross-linkages, all involving cysteine in a thioether bond.</Title>
-<Xref>DOI:10.1074/jbc.M107164200</Xref>
-<Xref>PMID:11555656</Xref>
-<Note>mass spectrometric and chemical characterization</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>C, E</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>GO:0019929</Xref>
-<Xref>PSI-MOD:00320</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__4-cysteinyl-glutamic acid (cys-glu)__c__e">CROSSLNK 4-cysteinyl-glutamic acid (Cys-Glu)</Feature>
-</Features>
-<Image src="/images/AA0315.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0315.PDB" />
-</Entry>
-<Entry id="AA0316">
-<Header>
-<Code>AA0316</Code>
-<Dates>
-<CreationDate>31-Dec-2001</CreationDate>
-<StrucRevDate>31-Dec-2001</StrucRevDate>
-<TextChngDate>20-May-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>cis-14-hydroxy-10,13-dioxo-7-heptadecenoic acid L-aspartate ester</Name>
-<AlternateName>barley lipid transfer protein modification</AlternateName>
-<SystematicName>(7Z,14Xi)-14-[(S)-3-amino-3-carboxy-propanoyl]oxy-10,13-dioxo-7-heptadecenoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 21 H 31 N 1 O 7</Formula>
-<Weight type="chemical">409.48</Weight>
-<Weight type="physical">409.210052</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0004">
-<Formula>C 17 H 26 N 0 O 4</Formula>
-<Weight type="chemical">294.39</Weight>
-<Weight type="physical">294.183109</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lindorff-Larsen, K.</Author>
-<Author>Lerche, M.H.</Author>
-<Author>Poulsen, F.M.</Author>
-<Author>Roepstorff, P.</Author>
-<Author>Winther, J.R.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 276, 33547-33553, 2001</Citation>
-<Title>Barley lipid transfer protein, LTP1, contains a new type of lipid-like post-translational modification.</Title>
-<Xref>DOI:10.1074/jbc.M104841200</Xref>
-<Xref>PMID:11435437</Xref>
-<Note>mass spectrometric, (1)H-NMR, and (13)C-NMR characterization</Note>
-</ReferenceBlock>
-<Comment>The stereochemistry for the second chiral center has not been resolved. The (14S) form is shown.</Comment>
-<SequenceCode>
-<SequenceSpec>D</SequenceSpec>
-<Xref>GO:0019930</Xref>
-<Xref>GO:0042050</Xref>
-<Xref>PSI-MOD:00321</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lipoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__cis-14-hydroxy-10,13-dioxo-7-heptadecenoic acid aspartate ester__d">LIPID Cis-14-hydroxy-10,13-dioxo-7-heptadecenoic acid aspartate ester</Feature>
-</Features>
-<Image src="/images/AA0316.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0316.PDB" />
-</Entry>
-<Entry id="AA0317">
-<Header>
-<Code>AA0317</Code>
-<Dates>
-<CreationDate>18-Jan-2002</CreationDate>
-<StrucRevDate>18-Jan-2002</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>1'-methyl-L-histidine</Name>
-<AlternateName>3-methylhistidine [misnomer]</AlternateName>
-<AlternateName>4-methyl-histidine [misnomer]</AlternateName>
-<AlternateName>N(epsilon)-methylhistidine</AlternateName>
-<AlternateName>N(tau)-methylhistidine</AlternateName>
-<AlternateName>tele-methylhistidine</AlternateName>
-<SystematicName>(S)-2-amino-3-(1-methyl-1H-imidazol-4-yl)propanoic acid</SystematicName>
-<Xref>CAS:332-80-9</Xref>
-<Xref>ChEBI:16367</Xref>
-<Xref>PDBHET:HIC</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 9 N 3 O 1</Formula>
-<Weight type="chemical">151.17</Weight>
-<Weight type="physical">151.074562</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0009">
-<Formula>C 1 H 2 N 0 O 0</Formula>
-<Weight type="chemical">14.03</Weight>
-<Weight type="physical">14.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Asatoor, A.M.</Author>
-<Author>Armstrong, M.D.</Author>
-</Authors>
-<Citation>Biochem. Biophys. Res. Commun. 26, 168-174, 1967</Citation>
-<Title>3-methyl histidine, a component of actin.</Title>
-<Xref>DOI:10.1016/0006-291X(67)90229-X</Xref>
-<Xref>PMID:6067661</Xref>
-<Note>identified as 1'-methylhistidine (tele-) and distinguished from 3'-methylhistidine (pros-) by ion exchange chromatography</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Edmondson, D.E.</Author>
-<Author>Kenney, W.C.</Author>
-<Author>Singer, T.P.</Author>
-</Authors>
-<Citation>Biochemistry 15, 2937-2945, 1976</Citation>
-<Title>Structural elucidation and properties of 8alpha-(N1-histidyl)riboflavin: the flavin component of thiamine dehydrogenase and beta-cyclopiazonate oxidocyclase.</Title>
-<Xref>DOI:10.1021/bi00659a001</Xref>
-<Xref>PMID:8076</Xref>
-<Note>chemical and spectrographic characterization of both 1'- and 3'-methylhistidine; the authors use biochemical rather than IUPAC numbering</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Anonymous />
-<Group>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN)</Group>
-</Authors>
-<Citation>Eur. J. Biochem. 138, 9-37, 1984</Citation>
-<Title>Nomenclature and symbolism for amino acids and peptides. Recommendations 1983.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1984.tb07877.x</Xref>
-<Xref>PMID:6692818</Xref>
-<Note>tele-, tau-, and pros-, pi-, nomenclature</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Raftery, M.J.</Author>
-<Author>Harrison, C.A.</Author>
-<Author>Alewood, P.</Author>
-<Author>Jones, A.</Author>
-<Author>Geczy, C.L.</Author>
-</Authors>
-<Citation>Biochem. J. 316, 285-293, 1996</Citation>
-<Title>Isolation of the murine S100 protein MRP14 (14 kDa migration-inhibitory-factor-related protein) from activated spleen cells: characterization of post-translational modifications and zinc binding.</Title>
-<Xref>PMID:8645219</Xref>
-<Note>mass spectrometric detection; chromatographic identification of PTC derivatives of 1'- and 3'-methylhistidine; the authors' source for the reference standard acknowledges that their name, 1'-methylhistidine, is a misnomer for the IUPAC standard name 3'-methylhistidine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yao, X.</Author>
-<Author>Grade, S.</Author>
-<Author>Wriggers, W.</Author>
-<Author>Rubenstein, P.A.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 274, 37443-37449, 1999</Citation>
-<Title>His(73), often methylated, is an important structural determinant for actin. A mutagenic analysis of HIS(73) of yeast actin.</Title>
-<Xref>DOI:10.1074/jbc.274.52.37443</Xref>
-<Xref>PMID:10601317</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Otterbein, L.R.</Author>
-<Author>Graceffa, P.</Author>
-<Author>Dominguez, R.</Author>
-</Authors>
-<Citation>Science 293, 708-711, 2001</Citation>
-<Title>The crystal structure of uncomplexed actin in the ADP state.</Title>
-<Xref>DOI:10.1126/science.1059700</Xref>
-<Xref>PMID:11474115</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Otterbein, L.R.</Author>
-<Author>Graceffa, P.</Author>
-<Author>Dominguez, R.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, May 2001</Citation>
-<Description>Uncomplexed actin.</Description>
-<Xref>PDB:1J6Z</Xref>
-<Note>X-ray diffraction, 1.54 angstroms</Note>
-</ReferenceBlock>
-<Comment>In the older biochemical literature this is usually called 3-methylhistidine. See also RESID:AA0073.</Comment>
-<Comment>The crystallographic designation for the substituted nitrogen is epsilon-2, E2.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>S-adenosyl-L-methionine:protein-L-histidine N-tele-methyltransferase (EC 2.1.1.85)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>H</SequenceSpec>
-<Xref>GO:0018021</Xref>
-<Xref>GO:0042038</Xref>
-<Xref>PSI-MOD:00322</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>methylated amino acid</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__tele-methylhistidine__h">MOD_RES Tele-methylhistidine</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="mod_res__methylhistidine__h">MOD_RES Methylhistidine</Feature>
-<Note>this UniProt feature is used when the isomeric structure has not been determined</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0317.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0317.PDB" />
-</Entry>
-<Entry id="AA0318">
-<Header>
-<Code>AA0318</Code>
-<Dates>
-<CreationDate>18-Jan-2002</CreationDate>
-<StrucRevDate>18-Jan-2002</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-lysine methyl ester</Name>
-<AlternateName>2,6-diaminohexanoic methyl ester</AlternateName>
-<AlternateName>alpha,epsilon-diaminocaproic methyl ester</AlternateName>
-<AlternateName>methyl L-lysinate</AlternateName>
-<SystematicName>methyl (S)-2,6-diaminohexanoate</SystematicName>
-<Xref>CAS:687-64-9</Xref>
-<Xref>ChEBI:21354</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 15 N 2 O 2</Formula>
-<Weight type="chemical">159.21</Weight>
-<Weight type="physical">159.113353</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 1 H 2 N 0 O 0</Formula>
-<Weight type="chemical">14.03</Weight>
-<Weight type="physical">14.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Zobel-Thropp, P.</Author>
-<Author>Yang, M.C.</Author>
-<Author>Machado, L.</Author>
-<Author>Clarke, S.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 275, 37150-37158, 2000</Citation>
-<Title>A novel post-translational modification of yeast elongation factor 1A. Methylesterification at the C terminus.</Title>
-<Xref>DOI:10.1074/jbc.M001005200</Xref>
-<Xref>PMID:10973948</Xref>
-<Note>chemical characterization</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>protein-lysine O-methyltransferase (EC 2.1.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0042034</Xref>
-<Xref>PSI-MOD:00323</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>methylated carboxyl end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__lysine methyl ester__k">MOD_RES Lysine methyl ester</Feature>
-</Features>
-<Image src="/images/AA0318.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0318.PDB" />
-</Entry>
-<Entry id="AA0319">
-<Header>
-<Code>AA0319</Code>
-<Dates>
-<CreationDate>31-Mar-2002</CreationDate>
-<StrucRevDate>31-Mar-2002</StrucRevDate>
-<TextChngDate>31-Mar-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-serinyl molybdenum bis(molybdopterin guanine dinucleotide)</Name>
-<AlternateName>2-amino-5,6-dimercapto-7-methyl-3,7,8a,9-tetrahydro-8-oxa-1,3,9,10-tetraazaanthracen-4-one guanosine dinucleotide</AlternateName>
-<SystematicName>bis[8-amino-1a,2,4a,5,6,7,10-heptahydro-2-(trihydrogen diphosphate 5'-ester with guanosine)methyl-6-oxo-3,4-disulfanyl-pteridino[6,7-5,6]pyranoato-S3,S4]-O3-serinyl-molybdenum oxide</SystematicName>
-<Xref>CAS:128007-95-4</Xref>
-<Xref>PDBHET:MGD</Xref>
-<Xref>PDBHET:MO</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 43 H 52 Mo 1 N 21 O 29 P 4 S 4</Formula>
-<Weight type="chemical">1675.09</Weight>
-<Weight type="physical">1676.012718</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 40 H 47 Mo 1 N 20 O 27 P 4 S 4</Formula>
-<Weight type="chemical">1588.01</Weight>
-<Weight type="physical">1588.980690</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Schindelin, H.</Author>
-<Author>Kisker, C.</Author>
-<Author>Hilton, J.</Author>
-<Author>Rajagopalan, K.V.</Author>
-<Author>Rees, D.C.</Author>
-</Authors>
-<Citation>Science 272, 1615-1621, 1996</Citation>
-<Title>Crystal structure of DMSO reductase: redox-linked changes in molybdopterin coordination.</Title>
-<Xref>DOI:10.1126/science.272.5268.1615</Xref>
-<Xref>PMID:8658134</Xref>
-<Note>X-ray diffraction, 1.30 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Li, H.-K.</Author>
-<Author>Temple, C.</Author>
-<Author>Rajagopalan, K.V.</Author>
-<Author>Schindelin, H.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 122, 7673-7680, 2000</Citation>
-<Title>The 1.3 Å Crystal Structure of Rhodobacter sphaeroides Dimethyl Sulfoxide Reductase Reveals Two Distinct Molybdenum Coordination Environments.</Title>
-<Xref>DOI:10.1021/ja000643e</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Li, H.K.</Author>
-<Author>Temple, K.</Author>
-<Author>Rajagopalan, K.V.</Author>
-<Author>Schindelin, H.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, April 2000</Citation>
-<Description>The crystal structure of Rhodobacter sphaeroides dimethylsulfoxide reductase reveals two distinct molybdenum coordination environments.</Description>
-<Xref>PDB:1EU1</Xref>
-<Note>X-ray diffraction, 1.30 angstroms</Note>
-</ReferenceBlock>
-<Comment>One possible structure of a reduced form (+4H) is shown. The fully reduced form would be 1a,2,3,4,4a,5,6,7,10-nonahydro. The fully oxidized form would be 2,6,7-trihydro.</Comment>
-<Comment>There is a distantly bound oxygen, which could exist as an oxide, a hydroxide or as a coordinating water. It is shown as an oxide.</Comment>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>GO:0042258</Xref>
-<Xref>PSI-MOD:00324</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>metalloprotein</Keyword>
-<Keyword>molybdenum</Keyword>
-<Keyword>molybdopterin</Keyword>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt" key="act_site____s">ACT_SITE</Feature>
-<Note>this UniProt feature lacks a descriptive representation</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0319.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0319.PDB" />
-</Entry>
-<Entry id="AA0320">
-<Header>
-<Code>AA0320</Code>
-<Dates>
-<CreationDate>31-Mar-2002</CreationDate>
-<StrucRevDate>31-Mar-2002</StrucRevDate>
-<TextChngDate>31-Mar-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>3-(methylthio)-L-asparagine</Name>
-<AlternateName>2,4-diamino-3-(methylsulfanyl)-4-oxobutanoic acid</AlternateName>
-<AlternateName>3-carboxamido-S-methyl-cysteine</AlternateName>
-<AlternateName>beta-(methylthio)asparagine</AlternateName>
-<SystematicName>(2R,3Xi)-2-amino-3-(methylsulfanyl)-4-butanediamic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 8 N 2 O 2 S 1</Formula>
-<Weight type="chemical">160.19</Weight>
-<Weight type="physical">160.030649</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0003">
-<Formula>C 1 H 2 N 0 O 0 S 1</Formula>
-<Weight type="chemical">46.09</Weight>
-<Weight type="physical">45.987721</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Carr, J.F.</Author>
-<Author>Hamburg, D.M.</Author>
-<Author>Gregory, S.T.</Author>
-<Author>Limbach, P.A.</Author>
-<Author>Dahlberg, A.E.</Author>
-</Authors>
-<Citation>J. Bacteriol. 188, 2020-2023, 2006</Citation>
-<Title>Effects of streptomycin resistance mutations on posttranslational modification of ribosomal protein S12.</Title>
-<Xref>DOI:10.1128/JB.188.5.2020-2023.2006</Xref>
-<Xref>PMID:16484214</Xref>
-<Note>noting that mutations of the S12 methylthioaspartic acid were lethal in Thermus thermophilus, the Bacillus subtilis S12 gene was resequenced and found to differ from the reported genome sequence</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lauber, M.A.</Author>
-<Author>Running, W.E.</Author>
-<Author>Reilly, J.P.</Author>
-</Authors>
-<Citation>J. Proteome Res. 8, 4193-4206, 2009</Citation>
-<Title>B. subtilis Ribosomal Proteins: Structural Homology and Post-Translational Modifications.</Title>
-<Xref>DOI:10.1021/pr801114k</Xref>
-<Xref>PMID:19653700</Xref>
-<Note>numerous genome sequencing errors are noted, including the S12 methylthioaspartic acid site; B. subtilis lacks the RimO modifying enzyme, and the S12 invariant aspartic acid is not modified</Note>
-</ReferenceBlock>
-<Comment>There is a second chiral center. The (2R,3R) form is shown.</Comment>
-<Comment>This modification was predicted for ribosomal protein S12 in Bacillus subtilis when the sequence in the original version of the genome was reported to have asparagine rather than aspartic acid at the position of the methylthioaspartic acid modification (see RESID:AA0232). Two groups independently confirmed that the genome sequence was erroroneous. The sequence in the revised genome has aspartic acid at that position.</Comment>
-<SequenceCode>
-<SequenceSpec>N</SequenceSpec>
-<Xref>GO:0042259</Xref>
-<Xref>PSI-MOD:00325</Xref>
-</SequenceCode>
-<Source>deprecated</Source>
-<Keywords>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0320.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0320.PDB" />
-</Entry>
-<Entry id="AA0321">
-<Header>
-<Code>AA0321</Code>
-<Dates>
-<CreationDate>24-May-2002</CreationDate>
-<StrucRevDate>24-May-2002</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-pyrrolysine</Name>
-<AlternateName>2-azanyl-6-[(2R,3R)-3-methyl-3,4-dihydro-2H-pyrrol-2-ylcarbonyl]azanylhexanoic acid</AlternateName>
-<AlternateName>monomethylamine methyltransferase cofactor lysine adduct</AlternateName>
-<AlternateName>N6-(4-methyl-1,2-didehydropyrrolidine-5-carboxyl)-L-lysine</AlternateName>
-<AlternateName>N6-(4-methyl-delta-1-pyrroline-5-carboxyl)-L-lysine</AlternateName>
-<AlternateName>N6-([(2R,3R)-3-methyl-3,4-dihydro-2H-pyrrol-2-yl]carbonyl)-L-lysine</AlternateName>
-<SystematicName>(2S)-2-amino-6-[(2R,3R)-3-methyl-3,4-dihydro-2H-pyrrol-2-ylcarbonyl]aminohexanoic acid</SystematicName>
-<Xref>CAS:448235-52-7</Xref>
-<Xref>ChEBI:21860</Xref>
-<Xref>PDBHET:BGX</Xref>
-<Xref>PDBHET:PYH</Xref>
-<Xref>PDBHET:X7O</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 12 H 19 N 3 O 2</Formula>
-<Weight type="chemical">237.30</Weight>
-<Weight type="physical">237.147727</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0321" label="PYL">
-<Formula>C 0 H 0 N 0 O 0</Formula>
-<Weight type="chemical">0.00</Weight>
-<Weight type="physical">0.000000</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0012" label="LYS">
-<Formula>C 6 H 7 N 1 O 1</Formula>
-<Weight type="chemical">109.13</Weight>
-<Weight type="physical">109.052764</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>James, C.M.</Author>
-<Author>Ferguson, T.K.</Author>
-<Author>Leykam, J.F.</Author>
-<Author>Krzycki, J.A.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 276, 34252-34258, 2001</Citation>
-<Title>The amber codon in the gene encoding the monomethylamine methyltransferase isolated from Methanosarcina barkeri is translated as a sense codon.</Title>
-<Xref>DOI:10.1074/jbc.M102929200</Xref>
-<Xref>PMID:11435424</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hao, B.</Author>
-<Author>Gong, W.</Author>
-<Author>Ferguson, T.K.</Author>
-<Author>James, C.M.</Author>
-<Author>Krzycki, J.A.</Author>
-<Author>Chan, M.K.</Author>
-</Authors>
-<Citation>Science 296, 1462-1466, 2002</Citation>
-<Title>A new UAG-encoded residue in the structure of a methanogen methyltransferase.</Title>
-<Xref>DOI:10.1126/science.1069556</Xref>
-<Xref>PMID:12029132</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Srinivasan, G.</Author>
-<Author>James, C.M.</Author>
-<Author>Krzycki, J.A.</Author>
-</Authors>
-<Citation>Science 296, 1459-1462, 2002</Citation>
-<Title>Pyrrolysine encoded by UAG in Archaea: charging of a UAG-decoding specialized tRNA.</Title>
-<Xref>DOI:10.1126/science.1069588</Xref>
-<Xref>PMID:12029131</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hao, B.</Author>
-<Author>Gong, W.</Author>
-<Author>Ferguson, T.K.</Author>
-<Author>James, C.M.</Author>
-<Author>Krzycki, J.A.</Author>
-<Author>Chan, M.K.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, February 2002</Citation>
-<Description>Crystal Structure of the Methanosarcina barkeri Monomethylamine Methyltransferase (MtmB).</Description>
-<Xref>PDB:1L2Q</Xref>
-<Note>X-ray diffraction, 1.55 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hao, B.</Author>
-<Author>Gong, W.</Author>
-<Author>Ferguson, T.K.</Author>
-<Author>James, C.M.</Author>
-<Author>Krzycki, J.A.</Author>
-<Author>Chan, M.K.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, January 2003</Citation>
-<Description>Crystal Structure of the Methanosarcina barkeri Monomethylamine Methyltransferase (MtmB).</Description>
-<Xref>PDB:1NTH</Xref>
-<Note>X-ray diffraction, 1.55 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Blight, S.K.</Author>
-<Author>Larue, R.C.</Author>
-<Author>Mahapatra, A.</Author>
-<Author>Longstaff, D.G.</Author>
-<Author>Chang, E.</Author>
-<Author>Zhao, G.</Author>
-<Author>Kang, P.T.</Author>
-<Author>Green-Church, K.B.</Author>
-<Author>Chan, M.K.</Author>
-<Author>Krzycki, J.A.</Author>
-</Authors>
-<Citation>Nature 431, 333-335, 2004</Citation>
-<Title>Direct charging of tRNA(CUA) with pyrrolysine in vitro and in vivo.</Title>
-<Xref>DOI:10.1038/nature02895</Xref>
-<Xref>PMID:15329732</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Polycarpo, C.</Author>
-<Author>Ambrogelly, A.</Author>
-<Author>Berube, A.</Author>
-<Author>Winbush, S.M.</Author>
-<Author>McCloskey, J.A.</Author>
-<Author>Crain, P.F.</Author>
-<Author>Wood, J.L.</Author>
-<Author>Soell, D.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 101, 12450-12454, 2004</Citation>
-<Title>An aminoacyl-tRNA synthetase that specifically activates pyrrolysine.</Title>
-<Xref>DOI:10.1073/pnas.0405362101</Xref>
-<Xref>PMID:15314242</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Krzycki, J.A.</Author>
-</Authors>
-<Citation>Curr. Opin. Chem. Biol. 8, 484-491, 2004</Citation>
-<Title>Function of genetically encoded pyrrolysine in corrinoid-dependent methylamine methyltransferases.</Title>
-<Xref>DOI:10.1016/j.cbpa.2004.08.012</Xref>
-<Xref>PMID:15450490</Xref>
-<Note>proposed functional role of pyrrolysine in methylamine methyltransferases</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Soares, J.A.</Author>
-<Author>Zhang, L.</Author>
-<Author>Pitsch, R.L.</Author>
-<Author>Kleinholz, N.M.</Author>
-<Author>Jones, R.B.</Author>
-<Author>Wolff, J.J.</Author>
-<Author>Amster, J.</Author>
-<Author>Green-Church, K.B.</Author>
-<Author>Krzycki, J.A.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 280, 36962-36969, 2005</Citation>
-<Title>The residue mass of L-pyrrolysine in three distinct methylamine methyltransferases.</Title>
-<Xref>DOI:10.1074/jbc.M506402200</Xref>
-<Xref>PMID:16096277</Xref>
-<Note>mass spectrometric characterization; the substituent at the 3 position on the pyrrol ring is established as a methyl group</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Heinemann, I.U.</Author>
-<Author>O'Donoghue, P.</Author>
-<Author>Madinger, C.</Author>
-<Author>Benner, J.</Author>
-<Author>Randau, L.</Author>
-<Author>Noren, C.J.</Author>
-<Author>Söll, D.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 106, 21103-21108, 2009</Citation>
-<Title>The appearance of pyrrolysine in tRNAHis guanylyltransferase by neutral evolution.</Title>
-<Xref>DOI:10.1073/pnas.0912072106</Xref>
-<Xref>PMID:19965368</Xref>
-<Note>report of a pyrrolysine apparently incorporated for termination suppression and not catalytically active</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gaston, M.A.</Author>
-<Author>Zhang, L.</Author>
-<Author>Green-Church, K.B.</Author>
-<Author>Krzycki, J.A.</Author>
-</Authors>
-<Citation>Nature 471, 647-650, 2011</Citation>
-<Title>The complete biosynthesis of the genetically encoded amino acid pyrrolysine from lysine.</Title>
-<Xref>DOI:10.1038/nature09918</Xref>
-<Xref>PMID:21455182</Xref>
-<Note>mass spectrometric identification of intermediate using (13)C and (15)N labels</Note>
-</ReferenceBlock>
-<Comment>Pyrrolysine is encoded by the UAG codon in some genetic systems.</Comment>
-<Comment>Although the single letter symbol O is recommended by IUBMB, most software applications fail to recognize it, and many sequence databases use the single letter symbol K.</Comment>
-<Comment>Proposed enzyme names are presented. There is evidence for the third reaction with an ornithine substrate, but not yet for the 3-methylornithine substrate, and the redox cofactor has not been identified.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>lysine--tRNA(Pyl) ligase (EC 6.1.1.25)</EnzymeName>
-<EnzymeName>pyrrolysine--tRNA(Pyl) ligase (EC 6.1.1.26)</EnzymeName>
-<EnzymeName>(3R)-3methyl-D-ornithine carboxy-aminomethylmutase, PylB (EC 5.4.99.-)</EnzymeName>
-<EnzymeName>(3R)-3-methyl-D-ornithine--L-lysine ligase, PylC (EC 6.3.2.-)</EnzymeName>
-<EnzymeName>N6-[(3R)-3-methyl-D-ornithinyl]-L-lysine N5-ornithine dehydrogenase, PylD (EC 1.4.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode link="PYL">
-<SequenceSpec>O</SequenceSpec>
-<Abbreviation>Pyl</Abbreviation>
-<Xref>GO:0030631</Xref>
-<Xref>PSI-MOD:01187</Xref>
-</SequenceCode>
-<SequenceCode link="LYS">
-<SequenceSpec>K</SequenceSpec>
-<Xref>PSI-MOD:00326</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>pyrrolysine</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="non_std__pyrrolysine__o">NON_STD Pyrrolysine</Feature>
-</Features>
-<Image src="/images/AA0321.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0321.PDB" />
-</Entry>
-<Entry id="AA0322">
-<Header>
-<Code>AA0322</Code>
-<Dates>
-<CreationDate>31-May-2002</CreationDate>
-<StrucRevDate>31-May-2002</StrucRevDate>
-<TextChngDate>31-Dec-2008</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>3-hydroxy-L-tryptophan</Name>
-<AlternateName>3-hydroxytryptophan</AlternateName>
-<AlternateName>beta-hydroxytryptophan</AlternateName>
-<SystematicName>(2S,3S)-2-amino-3-hydroxy-3-(1H-indol-3-yl)propanoic acid</SystematicName>
-<Xref>PDBHET:HTR</Xref>
-<Xref>PDBHET:HYD</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 11 H 10 N 2 O 2</Formula>
-<Weight type="chemical">202.21</Weight>
-<Weight type="physical">202.074228</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0018">
-<Formula>C 0 H 0 N 0 O 1</Formula>
-<Weight type="chemical">16.00</Weight>
-<Weight type="physical">15.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Choinowski, T.</Author>
-<Author>Blodig, W.</Author>
-<Author>Winterhalter, K.H.</Author>
-<Author>Piontek, K.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 286, 809-827, 1999</Citation>
-<Title>The crystal structure of lignin peroxidase at 1.70 A resolution reveals a hydroxy group on the Cbeta of tryptophan 171: a novel radical site formed during the redox cycle.</Title>
-<Xref>DOI:10.1006/jmbi.1998.2507</Xref>
-<Xref>PMID:10024453</Xref>
-<Note>X-ray diffraction, 1.7 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Choinowski, T.H.</Author>
-<Author>Piontek, K.</Author>
-<Author>Glumoff, T.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, November 1995</Citation>
-<Description>Lignin peroxidase (isozyme H2) pI=4.15.</Description>
-<Xref>PDB:1LLP</Xref>
-<Note>X-ray diffraction, 1.7 angstroms; it is uncertain whether this modification is required for enzyme activity, or is the byproduct of a redox cycle involving formation of a tryptophyl radical</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Liu, A.</Author>
-<Author>Ho, R.Y.</Author>
-<Author>Que Jr., L.</Author>
-<Author>Ryle, M.J.</Author>
-<Author>Phinney, B.S.</Author>
-<Author>Hausinger, R.P.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 123, 5126-5127, 2001</Citation>
-<Title>Alternative reactivity of an alpha-ketoglutarate-dependent iron(II) oxygenase: enzyme self-hydroxylation.</Title>
-<Xref>DOI:10.1021/ja005879x</Xref>
-<Xref>PMID:11457355</Xref>
-<Note>resonance Raman spectroscopic detection; mass spectrometric identification; the modification is shown to be autocatalytic, requires ascorbate, and converts alpha-ketoglutarate to succinate and CO2</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>W</SequenceSpec>
-<Xref>GO:0045325</Xref>
-<Xref>PSI-MOD:00327</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__3-hydroxytryptophan__w">MOD_RES 3-hydroxytryptophan</Feature>
-</Features>
-<Image src="/images/AA0322.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0322.PDB" />
-</Entry>
-<Entry id="AA0323">
-<Header>
-<Code>AA0323</Code>
-<Dates>
-<CreationDate>30-Jun-2002</CreationDate>
-<StrucRevDate>30-Jun-2002</StrucRevDate>
-<TextChngDate>30-Apr-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O4'-(phospho-3'-DNA)-L-tyrosine</Name>
-<AlternateName>O4'-L-tyrosine 3'-DNA phosphodiester</AlternateName>
-<SystematicName>(S)-2-amino-3-[4-(3'-deoxyribonucleic acid phosphonoxy)phenyl]propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 10 N 1 O 5 P 1 +</Formula>
-<Weight type="chemical">243.15 +</Weight>
-<Weight type="physical">243.029659 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0019">
-<Formula>C 0 H 1 N 0 O 3 P 1 +</Formula>
-<Weight type="chemical">79.98 +</Weight>
-<Weight type="physical">79.966331 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Evans, B.R.</Author>
-<Author>Chen, J.W.</Author>
-<Author>Parsons, R.L.</Author>
-<Author>Bauer, T.K.</Author>
-<Author>Teplow, D.B.</Author>
-<Author>Jayaram, M.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 265, 18504-18510, 1990</Citation>
-<Title>Identification of the active site tyrosine of Flp recombinase. Possible relevance of its location to the mechanism of recombination.</Title>
-<Xref>PMID:2211714</Xref>
-</ReferenceBlock>
-<Comment>The keyword "phosphoprotein" is not used with polynucleotide-linked intermediate modifications.</Comment>
-<SequenceCode>
-<SequenceSpec>Y</SequenceSpec>
-<Xref>GO:0045326</Xref>
-<Xref>PSI-MOD:00328</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>*phosphoprotein</Keyword>
-<Keyword>genome-linked protein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="act_site__o-(3&apos;-phospho-dna)-tyrosine intermediate__y">ACT_SITE O-(3'-phospho-DNA)-tyrosine intermediate</Feature>
-</Features>
-<Image src="/images/AA0323.GIF" alt="DUMMY.GIF" />
-</Entry>
-<Entry id="AA0324">
-<Header>
-<Code>AA0324</Code>
-<Dates>
-<CreationDate>30-Jun-2002</CreationDate>
-<StrucRevDate>30-Jun-2002</StrucRevDate>
-<TextChngDate>31-Dec-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>hydroxyheme-L-glutamate ester</Name>
-<AlternateName>5-hydroxymethyl protoporphyrin IX 5-glutamate ester</AlternateName>
-<AlternateName>cytochrome P450 CYP4A family heme cofactor</AlternateName>
-<SystematicName>[3-[(S)-(4-amino-4-carboxy)butanoyloxymethyl]-7,12-diethenyl-8,13,17-trimethyl-21H,23H-porphine-2,18-bis(2-carboxyethyl)-N21,N22,N23,N24]-ferrate</SystematicName>
-<Xref>COMe:BIM000314</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 39 Fe 1 H 37 N 5 O 7</Formula>
-<Weight type="chemical">743.60</Weight>
-<Weight type="physical">743.204236</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0006">
-<Formula>C 34 Fe 1 H 30 N 4 O 4</Formula>
-<Weight type="chemical">614.48</Weight>
-<Weight type="physical">614.161643</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hoch, U.</Author>
-<Author>Ortiz De Montellano, P.R.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 276, 11339-11346, 2001</Citation>
-<Title>Covalently linked heme in cytochrome P4504A fatty acid hydroxylases.</Title>
-<Xref>DOI:10.1074/jbc.M009969200</Xref>
-<Xref>PMID:11139583</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>LeBrun, L.A.</Author>
-<Author>Hoch, U.</Author>
-<Author>Ortiz de Montellano, P.R.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 277, 12755-12761, 2002</Citation>
-<Title>Autocatalytic mechanism and consequences of covalent heme attachment in the cytochrome P4504A family.</Title>
-<Xref>DOI:10.1074/jbc.M112155200</Xref>
-<Xref>PMID:11821421</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>LeBrun, L.A.</Author>
-<Author>Xu, F.Y.</Author>
-<Author>Kroetz, D.L.</Author>
-<Author>Ortiz de Montellano, P.R.</Author>
-</Authors>
-<Citation>Biochemistry 41, 5931-5937, 2002</Citation>
-<Title>Covalent attachment of the heme prosthetic group in the CYP4F cytochrome P450 family.</Title>
-<Xref>DOI:10.1021/bi025527y</Xref>
-<Xref>PMID:11980497</Xref>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>E</SequenceSpec>
-<Xref>GO:0045328</Xref>
-<Xref>PSI-MOD:00329</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chromoprotein</Keyword>
-<Keyword>heme</Keyword>
-<Keyword>hydroxylation</Keyword>
-<Keyword>iron</Keyword>
-<Keyword>metalloprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="binding__heme (covalent; via 1 link)__e">BINDING Heme (covalent; via 1 link)</Feature>
-</Features>
-<Image src="/images/AA0324.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0324.PDB" />
-</Entry>
-<Entry id="AA0325">
-<Header>
-<Code>AA0325</Code>
-<Dates>
-<CreationDate>12-Jul-2002</CreationDate>
-<StrucRevDate>12-Jul-2002</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>1'-(phospho-5'-guanosine)-L-histidine</Name>
-<AlternateName>L-histidine 5'-guanosine phosphoramidester</AlternateName>
-<AlternateName>L-histidine monoanhydride with 5'-guanylic acid</AlternateName>
-<AlternateName>N(tau)-5'-guanylic-L-histidine</AlternateName>
-<AlternateName>N1'-guanylylated histidine</AlternateName>
-<AlternateName>tele-5'-guanylic-L-histidine</AlternateName>
-<SystematicName>(2S)-2-amino-3-(1-(5'-adenosine phosphono)imidazol-4-yl)propanoic acid</SystematicName>
-<Xref>PDBHET:5GP</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 16 H 19 N 8 O 8 P 1</Formula>
-<Weight type="chemical">482.35</Weight>
-<Weight type="physical">482.106346</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0009">
-<Formula>C 10 H 12 N 5 O 7 P 1</Formula>
-<Weight type="chemical">345.21</Weight>
-<Weight type="physical">345.047434</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>O'Toole, G.A.</Author>
-<Author>Escalante-Semerena, J.C.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 270, 23560-23569, 1995</Citation>
-<Title>Purification and characterization of the bifunctional CobU enzyme of Salmonella typhimurium LT2. Evidence for a CobU-GMP intermediate.</Title>
-<Xref>DOI:10.1074/jbc.270.40.23560</Xref>
-<Xref>PMID:7559521</Xref>
-<Note>chemical evidence for guanylyl phosphoramide intermediate</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Thompson, T.B.</Author>
-<Author>Thomas, M.G.</Author>
-<Author>Escalante-Semerena, J.C.</Author>
-<Author>Rayment, I.</Author>
-</Authors>
-<Citation>Biochemistry 38, 12995-13005, 1999</Citation>
-<Title>Three-dimensional structure of adenosylcobinamide kinase/adenosylcobinamide phosphate guanylyltransferase (CobU) complexed with GMP: evidence for a substrate-induced transferase active site.</Title>
-<Xref>DOI:10.1021/bi990910x</Xref>
-<Xref>PMID:10529169</Xref>
-<Note>X-ray diffraction, 2.2 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Thompson, T.B.</Author>
-<Author>Thomas, M.G.</Author>
-<Author>Escalante-Semerena, J.C.</Author>
-<Author>Rayment, I.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, August 1999</Citation>
-<Description>The three-dimensional structure of adenosylcobinamide kinase/adenosylcobinamide phosphate guanylyltransferase (CobU) complexed with GMP: evidence for a substrate-induced transferase active site.</Description>
-<Xref>PDB:1C9K</Xref>
-<Note>X-ray diffraction, 2.2 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Thomas, M.G.</Author>
-<Author>Thompson, T.B.</Author>
-<Author>Rayment, I.</Author>
-<Author>Escalante-Semerena, J.C.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 275, 27576-27586, 2000</Citation>
-<Title>Analysis of the adenosylcobinamide kinase/adenosylcobinamide-phosphate guanylyltransferase (CobU) enzyme of Salmonella typhimurium LT2. Identification of residue His-46 as the site of guanylylation.</Title>
-<Xref>DOI:10.1074/jbc.M000977200</Xref>
-<Xref>PMID:10869342</Xref>
-<Note>location of histidine modification</Note>
-</ReferenceBlock>
-<Comment>It is not known whether the phosphoramide bond is formed with the tele- or pros-nitrogen of histidine. The tele-linked form is presented.</Comment>
-<SequenceCode>
-<SequenceSpec>H</SequenceSpec>
-<Xref>GO:0045427</Xref>
-<Xref>PSI-MOD:00330</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="act_site__gmp-histidine intermediate__h">ACT_SITE GMP-histidine intermediate</Feature>
-</Features>
-<Image src="/images/AA0325.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0325.PDB" />
-</Entry>
-<Entry id="AA0326">
-<Header>
-<Code>AA0326</Code>
-<Dates>
-<CreationDate>02-Aug-2002</CreationDate>
-<StrucRevDate>02-Aug-2002</StrucRevDate>
-<TextChngDate>31-Dec-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>tetrakis-L-cysteinyl triiron tetrasulfide</Name>
-<AlternateName>bis[bis-L-cysteinyl iron disulfido]iron</AlternateName>
-<AlternateName>tetra-mu-sulfido tetrakis-S-L-cysteinyl triiron</AlternateName>
-<AlternateName>tetrakis-L-cysteinyl linear [3Fe-4S] cluster</AlternateName>
-<AlternateName>tetrakis-L-cysteinyl triiron tetrasulfide D2 cluster</AlternateName>
-<SystematicName>di-mu-1:2kappaS-sulfido di-mu-2:3kappaS-sulfido iron bis(bis-S-cysteinyliron)</SystematicName>
-<Xref>COMe:BIM000318</Xref>
-<Xref>PDBHET:F3S</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 12 Fe 3 H 16 N 4 O 4 S 8</Formula>
-<FormalCharge>3-</FormalCharge>
-<Weight type="chemical">704.30</Weight>
-<Weight type="physical">703.700181</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005 AA0005 AA0005">
-<Formula>C 0 Fe 3 H -4 N 0 O 0 S 4</Formula>
-<FormalCharge>3-</FormalCharge>
-<Weight type="chemical">291.74</Weight>
-<Weight type="physical">291.663442</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kennedy, M.C.</Author>
-<Author>Kent, T.A.</Author>
-<Author>Emptage, M.</Author>
-<Author>Merkle, H.</Author>
-<Author>Beinert, H.</Author>
-<Author>Munck, E.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 259, 14463-14471, 1984</Citation>
-<Title>Evidence for the formation of a linear [3Fe-4S] cluster in partially unfolded aconitase.</Title>
-<Xref>PMID:6094558</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Plank, D.W.</Author>
-<Author>Kennedy, M.C.</Author>
-<Author>Beinert, H.</Author>
-<Author>Howard, J.B.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 264, 20385-20393, 1989</Citation>
-<Title>Cysteine labeling studies of beef heart aconitase containing a 4Fe, a cubane 3Fe, or a linear 3Fe cluster.</Title>
-<Xref>PMID:2511202</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gailer, J.</Author>
-<Author>George, G.N.</Author>
-<Author>Pickering, I.J.</Author>
-<Author>Prince, R.C.</Author>
-<Author>Kohlhepp, P.</Author>
-<Author>Zhang, D.</Author>
-<Author>Walker, F.A.</Author>
-<Author>Winzerling, J.J.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 123, 10121-10122, 2001</Citation>
-<Title>Human cytosolic iron regulatory protein 1 contains a linear iron-sulfur cluster.</Title>
-<Xref>DOI:10.1021/ja0158915</Xref>
-<Xref>PMID:11592901</Xref>
-<Note>X-ray absorption fine structure spectroscopy</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Jones, K.</Author>
-<Author>Gomes, C.M.</Author>
-<Author>Huber, H.</Author>
-<Author>Teixeira, M.</Author>
-<Author>Wittung-Stafshede, P.</Author>
-</Authors>
-<Citation>J. Biol. Inorg. Chem. 7, 357-362, 2002</Citation>
-<Title>Formation of a linear [3Fe-4S] cluster in a seven-iron ferredoxin triggered by polypeptide unfolding.</Title>
-<Xref>DOI:10.1007/s00775-001-0304-4</Xref>
-<Xref>PMID:11941493</Xref>
-</ReferenceBlock>
-<Comment>The linear 3Fe-4S cluster may form from the reconfiguration of trigonal 3Fe-4S clusters. See RESID:AA0139.</Comment>
-<SequenceCode>
-<SequenceSpec>C, C, C, C</SequenceSpec>
-<Condition>cross-link 4</Condition>
-<Xref>GO:0045459</Xref>
-<Xref>PSI-MOD:00331</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>3Fe-4S</Keyword>
-<Keyword>iron-sulfur protein</Keyword>
-<Keyword>metalloprotein</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0326.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0326.PDB" />
-</Entry>
-<Entry id="AA0327">
-<Header>
-<Code>AA0327</Code>
-<Dates>
-<CreationDate>06-Sep-2002</CreationDate>
-<StrucRevDate>06-Sep-2002</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>omega-N-glucosyl-L-arginine</Name>
-<AlternateName>NG-beta-D-glucosylarginine</AlternateName>
-<AlternateName>omega-N-(beta-D-glucosyl)-L-arginine</AlternateName>
-<AlternateName>omega-N-glycosyl-L-arginine</AlternateName>
-<SystematicName>(2S)-2-amino-5-(beta-D-glucopyranosyl[imino(methylamino)methyl]amino)pentanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 12 H 22 N 4 O 6</Formula>
-<Weight type="chemical">318.33</Weight>
-<Weight type="physical">318.153934</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0002">
-<Formula>C 6 H 10 N 0 O 5</Formula>
-<Weight type="chemical">162.14</Weight>
-<Weight type="physical">162.052823</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Singh, D.G.</Author>
-<Author>Lomako, J.</Author>
-<Author>Lomako, W.M.</Author>
-<Author>Whelan, W.J.</Author>
-<Author>Meyer, H.E.</Author>
-<Author>Serwe, M.</Author>
-<Author>Metzger, J.W.</Author>
-</Authors>
-<Citation>FEBS Lett. 376, 61-64, 1995</Citation>
-<Title>beta-Glucosylarginine: a new glucose-protein bond in a self-glucosylating protein from sweet corn.</Title>
-<Xref>DOI:10.1016/0014-5793(95)01247-6</Xref>
-<Xref>PMID:8521968</Xref>
-<Note>sequence analysis; mass spectrometric and linkage analysis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Delgado, I.J.</Author>
-<Author>Wang, Z.</Author>
-<Author>de Rocher, A.</Author>
-<Author>Keegstra, K.</Author>
-<Author>Raikhel, N.V.</Author>
-</Authors>
-<Citation>Plant Physiol. 116, 1339-1350, 1998</Citation>
-<Title>Cloning and characterization of AtRGP1. A reversibly autoglycosylated arabidopsis protein implicated in cell wall biosynthesis.</Title>
-<Xref>DOI:10.1104/pp.116.4.1339</Xref>
-<Xref>PMID:9536051</Xref>
-</ReferenceBlock>
-<Comment>Although proposed as the origin for plant starch, the anomeric isomer was beta, rather than alpha, and only a monosaccharide was observed.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>amylogenin glucosyltransferase (EC 2.4.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>R</SequenceSpec>
-<Xref>GO:0042543</Xref>
-<Xref>PSI-MOD:00332</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__n-linked (glc...) arginine__r">CARBOHYD N-linked (Glc...) arginine</Feature>
-</Features>
-<Image src="/images/AA0327.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0327.PDB" />
-</Entry>
-<Entry id="AA0328">
-<Header>
-<Code>AA0328</Code>
-<Dates>
-<CreationDate>11-Oct-2002</CreationDate>
-<StrucRevDate>11-Oct-2002</StrucRevDate>
-<TextChngDate>25-Feb-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>(3-aminopropyl)(L-aspartyl-1-amino)phosphoryl-5'-adenosine</Name>
-<AlternateName>9-(5'-O-[(3-aminopropoxy)(L-aspart-1-ylamino)phosphoryl]-beta-D-ribofuranosyl)adenine</AlternateName>
-<AlternateName>microcin C7 asparagine modification</AlternateName>
-<AlternateName>N-(aspart-1-yl)-O-(3-aminopropyl)-O-(5'-adenosyl)phosphoramide</AlternateName>
-<SystematicName>5'-O-[(3-aminopropoxy)(L-aspart-1-ylamino)phosphoryl]adenosine</SystematicName>
-<Xref>ChEBI:60869</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 17 H 26 N 8 O 9 P 1</Formula>
-<Weight type="chemical">517.42</Weight>
-<Weight type="physical">517.156036</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0003">
-<Formula>C 13 H 19 N 6 O 6 P 1</Formula>
-<Weight type="chemical">386.30</Weight>
-<Weight type="physical">386.110369</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gonzalez-Pastor, J.E.</Author>
-<Author>San Millan, J.L.</Author>
-<Author>Moreno, F.</Author>
-</Authors>
-<Citation>Nature 369, 281, 1994</Citation>
-<Title>The smallest known gene.</Title>
-<Xref>DOI:10.1038/369281a0</Xref>
-<Xref>PMID:8183363</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Metlitskaya, A.Z.</Author>
-<Author>Katrukha, G.S.</Author>
-<Author>Shashkov, A.S.</Author>
-<Author>Zaitsev, D.A.</Author>
-<Author>Egorov, Ts.A.</Author>
-<Author>Khmel, I.A.</Author>
-</Authors>
-<Citation>FEBS Lett. 357, 235-238, 1995</Citation>
-<Title>Structure of microcin C51, a new antibiotic with a broad spectrum of activity.</Title>
-<Xref>DOI:10.1016/0014-5793(94)01345-2</Xref>
-<Xref>PMID:7835418</Xref>
-<Note>the proposed structure of the peptide has an N4-propylphosphoryl-5'-ribosylisopurine asparagine, and a highly unstable aminoxy-threonine; the initials of "T.A. Egorov" in the PubMed citation are corrected</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Guijarro, J.I.</Author>
-<Author>Gonzalez-Pastor, J.E.</Author>
-<Author>Baleux, F.</Author>
-<Author>San Millan, J.L.</Author>
-<Author>Castilla, M.A.</Author>
-<Author>Rico, M.</Author>
-<Author>Moreno, F.</Author>
-<Author>Delepierre, M.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 270, 23520-23532, 1995</Citation>
-<Title>Chemical structure and translation inhibition studies of the antibiotic microcin C7.</Title>
-<Xref>DOI:10.1074/jbc.270.40.23520</Xref>
-<Xref>PMID:7559516</Xref>
-<Note>the proposed structure of the peptide has a relatively unstable aspartyl-phosphoramidate diester with 3-aminopropanol and 5'-adenosine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Roush, R.F.</Author>
-<Author>Nolan, E.M.</Author>
-<Author>Löhr, F.</Author>
-<Author>Walsh, C.T.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 130, 3603-3609, 2008</Citation>
-<Title>Maturation of an Escherichia coli ribosomal peptide antibiotic by ATP-consuming N-P bond formation in microcin C7.</Title>
-<Xref>DOI:10.1021/ja7101949</Xref>
-<Xref>PMID:18290647</Xref>
-<Note>biosynthesis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Regni, C.A.</Author>
-<Author>Roush, R.F.</Author>
-<Author>Miller, D.J.</Author>
-<Author>Nourse, A.</Author>
-<Author>Walsh, C.T.</Author>
-<Author>Schulman, B.A.</Author>
-</Authors>
-<Citation>EMBO J. 28, 1953-1964, 2009</Citation>
-<Title>How the MccB bacterial ancestor of ubiquitin E1 initiates biosynthesis of the microcin C7 antibiotic.</Title>
-<Xref>DOI:10.1038/emboj.2009.146</Xref>
-<Xref>PMID:19494832</Xref>
-<Note>biosynthesis</Note>
-</ReferenceBlock>
-<Comment>The structure shown has been independently confirmed. Asparagine is converted to an aspartyl-1-amide by a process requiring two ATP molecules and the formation of a peptidyl-succinimide intermediate.</Comment>
-<Comment>The phosphorus atom is a chiral center that has not been resolved.</Comment>
-<SequenceCode>
-<SequenceSpec>N</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0046550</Xref>
-<Xref>PSI-MOD:00333</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__aspartic acid 1-[(3-aminopropyl)(5'-adenosyl)phosphono]amide__n">MOD_RES Aspartic acid 1-[(3-aminopropyl)(5'-adenosyl)phosphono]amide</Feature>
-</Features>
-<Image src="/images/AA0328.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0328.PDB" />
-</Entry>
-<Entry id="AA0329">
-<Header>
-<Code>AA0329</Code>
-<Dates>
-<CreationDate>31-Dec-2002</CreationDate>
-<StrucRevDate>31-Dec-2009</StrucRevDate>
-<TextChngDate>30-Apr-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>1'-heme-L-histidine</Name>
-<AlternateName>2-[1-(N1'-histidyl)ethyl]protoporphyrin IX</AlternateName>
-<AlternateName>N(epsilon)-histidyl heme</AlternateName>
-<AlternateName>N(tau)-histidyl heme</AlternateName>
-<AlternateName>N1'-histidyl heme</AlternateName>
-<AlternateName>tele-histidyl heme</AlternateName>
-<SystematicName>(S)-[7-ethenyl-12-[1-((2-amino-2-carboxyethyl)-1H-imidazol-1-yl)ethyl]-3,8,13,17-tetramethyl-21H,23H-porphine-2,18-bis(2-carboxyethyl)-N21,N22,N23,N24]-ferrate</SystematicName>
-<Xref>COMe:BIM000351</Xref>
-<Xref>PDBHET:HEM</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 40 Fe 1 H 39 N 7 O 5</Formula>
-<Weight type="chemical">753.64</Weight>
-<Weight type="physical">753.236205</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0009">
-<Formula>C 34 Fe 1 H 32 N 4 O 4</Formula>
-<Weight type="chemical">616.50</Weight>
-<Weight type="physical">616.177293</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Scott, N.L.</Author>
-<Author>Falzone, C.J.</Author>
-<Author>Vuletich, D.A.</Author>
-<Author>Zhao, J.</Author>
-<Author>Bryant, D.A.</Author>
-<Author>Lecomte, J.T.</Author>
-</Authors>
-<Citation>Biochemistry 41, 6902-6910, 2002</Citation>
-<Title>Truncated hemoglobin from the cyanobacterium Synechococcus sp. PCC 7002: evidence for hexacoordination and covalent adduct formation in the ferric recombinant protein.</Title>
-<Xref>DOI:10.1021/bi025609m</Xref>
-<Xref>PMID:12033922</Xref>
-<Note>NOESY, 2QF-COSY, and TOCSY NMR detection; it is possible that the cross-link forms abnormally in the recombinant system</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Vu, B.C.</Author>
-<Author>Jones, A.D.</Author>
-<Author>Lecomte, J.T.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 124, 8544-8545, 2002</Citation>
-<Title>Novel histidine-heme covalent linkage in a hemoglobin.</Title>
-<Xref>DOI:10.1021/ja026569c</Xref>
-<Xref>PMID:12121092</Xref>
-<Note>mass spectrometric characterization; (1)H-(15)N-HMQC NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Falzone, C.J.</Author>
-<Author>Vu, B.C.</Author>
-<Author>Scott, N.L.</Author>
-<Author>Lecomte, J.T.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 324, 1015-1029, 2002</Citation>
-<Title>The solution structure of the recombinant hemoglobin from the cyanobacterium Synechocystis sp. PCC 6803 in its hemichrome state.</Title>
-<Xref>DOI:10.1016/S0022-2836(02)01093-8</Xref>
-<Xref>PMID:12470956</Xref>
-<Note>(1)H-NMR and (15)N-NMR characterization; the initials of "C.B. Vu" in the PubMed citation are corrected</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Falzone, C.J.</Author>
-<Author>Vu, B.C.</Author>
-<Author>Scott, N.L.</Author>
-<Author>Lecomte, J.T.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, September 2002</Citation>
-<Description>Solution structure of the recombinant hemoglobin from the cyanobacterium Synechocystis sp. PCC 6803 in its hemichrome state.</Description>
-<Xref>PDB:1MWB</Xref>
-<Note>conformation by (1)H-NMR and (15)N-NMR</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hoy, J.A.</Author>
-<Author>Kundu, S.</Author>
-<Author>Trent III, J.T.</Author>
-<Author>Ramaswamy, S.</Author>
-<Author>Hargrove, M.S.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 279, 16535-16542, 2004</Citation>
-<Title>The crystal structure of Synechocystis hemoglobin with a covalent heme linkage.</Title>
-<Xref>DOI:10.1074/jbc.M313707200</Xref>
-<Xref>PMID:14736872</Xref>
-<Note>X-ray diffraction, 1.8 angstroms; the spelling "Trent, J.T. 3rd", in the PubMed citation is corrected</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hoy, J.A.</Author>
-<Author>Kundu, S.</Author>
-<Author>Trent, J.T.</Author>
-<Author>Ramaswamy, S.</Author>
-<Author>Hargrove, M.S.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, December 2003</Citation>
-<Description>Crystal structure of Synechocystis hemoglobin with a covalent heme linkage.</Description>
-<Xref>PDB:1RTX</Xref>
-<Note>X-ray diffraction, 1.8 angstroms</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>H</SequenceSpec>
-<Xref>GO:0046805</Xref>
-<Xref>PSI-MOD:00334</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chromoprotein</Keyword>
-<Keyword>heme</Keyword>
-<Keyword>iron</Keyword>
-<Keyword>metalloprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="binding__heme (covalent; via tele nitrogen)__h">BINDING Heme (covalent; via tele nitrogen)</Feature>
-</Features>
-<Image src="/images/AA0329.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0329.PDB" />
-</Entry>
-<Entry id="AA0330">
-<Header>
-<Code>AA0330</Code>
-<Dates>
-<CreationDate>31-Dec-2002</CreationDate>
-<StrucRevDate>31-Dec-2002</StrucRevDate>
-<TextChngDate>31-Mar-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>3-methyl-L-lanthionine sulfoxide</Name>
-<AlternateName>(2S,3S,4Xi,6R)-2,6-diamino-3-methyl-4-oxo-4-thiaheptanedioic acid</AlternateName>
-<AlternateName>3-methyl-L-lanthionine S-oxide</AlternateName>
-<AlternateName>S-oxy-3-methyllanthionine</AlternateName>
-<SystematicName>(2S,3S,SXi)-2-amino-3-([(R)-2-amino-2-carboxyethyl]sulfinyl)butanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 10 N 2 O 3 S 1</Formula>
-<Weight type="chemical">202.23</Weight>
-<Weight type="physical">202.041213</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0017">
-<Formula>C 0 H -2 N 0 O 0 S 0</Formula>
-<Weight type="chemical">-2.02</Weight>
-<Weight type="physical">-2.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Zimmermann, N.</Author>
-<Author>Metzger, J.W.</Author>
-<Author>Jung, G.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 228, 786-797, 1995</Citation>
-<Title>The tetracyclic lantibiotic actagardine. 1H-NMR and 13C-NMR assignments and revised primary structure.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1995.tb20324.x</Xref>
-<Xref>PMID:7737178</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Zimmermann, N.</Author>
-<Author>Jung, G.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 246, 809-819, 1997</Citation>
-<Title>The three-dimensional solution structure of the lantibiotic murein-biosynthesis-inhibitor actagardine determined by NMR.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1997.00809.x</Xref>
-<Xref>PMID:9219543</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Zimmermann, N.</Author>
-<Author>Jung, G.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, May 1997</Citation>
-<Description>NMR structure of the lantibiotic actagardine, 15 structures.</Description>
-<Xref>PDB:1AJ1</Xref>
-<Note>conformation by (1)H-NMR; the sulfoxide is not modeled in the NMR-determined structure</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Shi, Y.</Author>
-<Author>Bueno, A.</Author>
-<Author>van der Donk, W.A.</Author>
-</Authors>
-<Citation>Chem. Commun. (Camb.) 48, 10966-10968, 2012</Citation>
-<Title>Heterologous production of the lantibiotic Ala(0)actagardine in Escherichia coli.</Title>
-<Xref>DOI:10.1039/c2cc36336d</Xref>
-<Xref>PMID:23034674</Xref>
-<Note>use of GarO, a luciferase-like monooxygenase, to produce the sulfoxide</Note>
-</ReferenceBlock>
-<Comment>The S-oxide of 3-methyl-L-lanthionine is a chiral center, and the stereoisomer has not been determined.</Comment>
-<SequenceCode>
-<SequenceSpec>C, T</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>GO:0046804</Xref>
-<Xref>PSI-MOD:00335</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lanthionine</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__beta-methyllanthionine sulfoxide (thr-cys)__t__c">CROSSLNK Beta-methyllanthionine sulfoxide (Thr-Cys)</Feature>
-</Features>
-<Image src="/images/AA0330.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0330.PDB" />
-</Entry>
-<Entry id="AA0331">
-<Header>
-<Code>AA0331</Code>
-<Dates>
-<CreationDate>21-Feb-2003</CreationDate>
-<StrucRevDate>21-Feb-2003</StrucRevDate>
-<TextChngDate>31-Dec-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>tris-L-cysteinyl L-aspartato diiron disulfide</Name>
-<SystematicName>di-mu-sulfido(bis-S-cysteinyliron)(S-cysteinyl-O4-aspartatoiron)</SystematicName>
-<Xref>COMe:BIM000062</Xref>
-<Xref>PDBHET:FES</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 13 Fe 2 H 16 N 4 O 6 S 5</Formula>
-<FormalCharge>2-</FormalCharge>
-<Weight type="chemical">596.28</Weight>
-<Weight type="physical">595.838311</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005 AA0005 AA0004">
-<Formula>C 0 Fe 2 H -4 N 0 O 0 S 2</Formula>
-<FormalCharge>2-</FormalCharge>
-<Weight type="chemical">171.78</Weight>
-<Weight type="physical">171.783814</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Werth, M.T.</Author>
-<Author>Sices, H.</Author>
-<Author>Cecchini, G.</Author>
-<Author>Schroeder, I.</Author>
-<Author>Lasage, S.</Author>
-<Author>Gunsalus, R.P.</Author>
-<Author>Johnson, M.K.</Author>
-</Authors>
-<Citation>FEBS Lett. 299, 1-4, 1992</Citation>
-<Title>Evidence for non-cysteinyl coordination of the [2Fe-2S] cluster in Escherichia coli succinate dehydrogenase.</Title>
-<Xref>DOI:10.1016/0014-5793(92)80086-V</Xref>
-<Xref>PMID:1312028</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Meyer, J.</Author>
-<Author>Fujinaga, J.</Author>
-<Author>Gaillard, J.</Author>
-<Author>Lutz, M.</Author>
-</Authors>
-<Citation>Biochemistry 33, 13642-13650, 1994</Citation>
-<Title>Mutated forms of the [2Fe-2S] ferredoxin from Clostridium pasteurianum with noncysteinyl ligands to the iron-sulfur cluster.</Title>
-<Xref>DOI:10.1021/bi00250a014</Xref>
-<Xref>PMID:7947772</Xref>
-<Note>an atypical 2Fe-2S cluster; three of four ligands are determined</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hagen, W.R.</Author>
-<Author>Silva, P.J.</Author>
-<Author>Amorim, M.A.</Author>
-<Author>Hagedoorn, P.L.</Author>
-<Author>Wassink, H.</Author>
-<Author>Haaker, H.</Author>
-<Author>Robb, F.T.</Author>
-</Authors>
-<Citation>J. Biol. Inorg. Chem. 5, 527-534, 2000</Citation>
-<Title>Novel structure and redox chemistry of the prosthetic groups of the iron-sulfur flavoprotein sulfide dehydrogenase from Pyrococcus furiosus; evidence for a [2Fe-2S] cluster with Asp(Cys)3 ligands.</Title>
-<Xref>DOI:10.1007/s007750050013</Xref>
-<Xref>PMID:10968624</Xref>
-</ReferenceBlock>
-<Comment>The occurrence of aspartic acid rather than cysteine in an otherwise strongly conserved homology domain known to bind the 2Fe-2S cluster in other proteins suggests that aspartic acid may also bind iron-sulfur clusters.</Comment>
-<SequenceCode>
-<SequenceSpec>C, C, C, D</SequenceSpec>
-<Condition>cross-link 4</Condition>
-<Xref>GO:0046869</Xref>
-<Xref>PSI-MOD:00336</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>2Fe-2S</Keyword>
-<Keyword>iron-sulfur protein</Keyword>
-<Keyword>metalloprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="metal__iron-sulfur (2fe-2s)__d">METAL Iron-sulfur (2Fe-2S)</Feature>
-</Features>
-<Image src="/images/AA0331.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0331.PDB" />
-</Entry>
-<Entry id="AA0332">
-<Header>
-<Code>AA0332</Code>
-<Dates>
-<CreationDate>14-Mar-2003</CreationDate>
-<StrucRevDate>14-Mar-2003</StrucRevDate>
-<TextChngDate>20-Nov-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-carbamoyl-L-cysteine</Name>
-<AlternateName>2-amino-3-(aminocarbonyl)sulfanylpropanoic acid</AlternateName>
-<AlternateName>2-amino-3-(aminocarbonyl)thiopropanoic acid</AlternateName>
-<AlternateName>alpha-amino-beta-carbamylthiopropionic acid</AlternateName>
-<AlternateName>beta-carbamylthioalanine</AlternateName>
-<AlternateName>S-(aminocarbonyl)cysteine</AlternateName>
-<AlternateName>S-carbamoylcysteine</AlternateName>
-<AlternateName>S-carbamylcysteine</AlternateName>
-<AlternateName>S-cysteinyl carbamate ester</AlternateName>
-<SystematicName>(R)-2-amino-3-(carbamoylsulfanyl)propanoic acid</SystematicName>
-<Xref>CAS:2072-71-1</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 6 N 2 O 2 S 1</Formula>
-<Weight type="chemical">146.16</Weight>
-<Weight type="physical">146.014998</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 1 H 1 N 1 O 1 S 0</Formula>
-<Weight type="chemical">43.02</Weight>
-<Weight type="physical">43.005814</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Anderson, P.M.</Author>
-<Author>Carlson, J.D.</Author>
-</Authors>
-<Citation>Biochemistry 14, 3688-3694, 1975</Citation>
-<Title>Reversible reaction of cyanate with a reactive sulfhydryl group at the glutamine binding site of carbamyl phosphate synthetase.</Title>
-<Xref>DOI:10.1021/bi00687a027</Xref>
-<Xref>PMID:240389</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Reissmann, S.</Author>
-<Author>Hochleitner, E.</Author>
-<Author>Wang, H.</Author>
-<Author>Paschos, A.</Author>
-<Author>Lottspeich, F.</Author>
-<Author>Glass, R.S.</Author>
-<Author>Bock, A.</Author>
-</Authors>
-<Citation>Science 299, 1067-1070, 2003</Citation>
-<Title>Taming of a Poison: Biosynthesis of the NiFe-Hydrogenase Cyanide Ligands.</Title>
-<Xref>DOI:10.1126/science.1080972</Xref>
-<Xref>PMID:12586941</Xref>
-<Note>the modification is observed when dehydration, an auto-catalyzed process using ATP in the HypE protein, is blocked</Note>
-</ReferenceBlock>
-<Comment>This modification can undergo dehydration to produce S-cyanocysteine. See RESID:AA0333.</Comment>
-<Comment>Carbamoylation of the sulfhydryl group can be artifactual, in particular when urea buffers are used.</Comment>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>GO:0046891</Xref>
-<Xref>PSI-MOD:00337</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="mod_res__s-carbamoylcysteine__c">MOD_RES S-carbamoylcysteine</Feature>
-</Features>
-<Image src="/images/AA0332.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0332.PDB" />
-</Entry>
-<Entry id="AA0333">
-<Header>
-<Code>AA0333</Code>
-<Dates>
-<CreationDate>14-Mar-2003</CreationDate>
-<StrucRevDate>14-Mar-2003</StrucRevDate>
-<TextChngDate>30-Sep-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-cyano-L-cysteine</Name>
-<AlternateName>alpha-amino-beta-thiocyanatopropionic acid</AlternateName>
-<AlternateName>beta-thiocyanatoalanine</AlternateName>
-<AlternateName>S-cyanocysteine</AlternateName>
-<AlternateName>serine thiocyanic acid ester</AlternateName>
-<SystematicName>(2R)-2-amino-3-thiocyanatopropanoic acid</SystematicName>
-<Xref>CAS:5652-31-3</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 4 N 2 O 1 S 1</Formula>
-<Weight type="chemical">128.15</Weight>
-<Weight type="physical">128.004434</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 1 H -1 N 1 O 0 S 0</Formula>
-<Weight type="chemical">25.01</Weight>
-<Weight type="physical">24.995249</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Degani, Y.</Author>
-<Author>Patchornik, A.</Author>
-</Authors>
-<Citation>Biochemistry 13, 1-11, 1974</Citation>
-<Title>Cyanylation of sulfhydryl groups by 2-nitro-5-thiocyanobenzoic acid. High-yield modification and cleavage of peptides at cysteine residues.</Title>
-<Xref>DOI:10.1021/bi00698a001</Xref>
-<Xref>PMID:4808702</Xref>
-<Note>modification by reagent of cysteine in the presence of cystine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Reissmann, S.</Author>
-<Author>Hochleitner, E.</Author>
-<Author>Wang, H.</Author>
-<Author>Paschos, A.</Author>
-<Author>Lottspeich, F.</Author>
-<Author>Glass, R.S.</Author>
-<Author>Bock, A.</Author>
-</Authors>
-<Citation>Science 299, 1067-1070, 2003</Citation>
-<Title>Taming of a Poison: Biosynthesis of the NiFe-Hydrogenase Cyanide Ligands.</Title>
-<Xref>DOI:10.1126/science.1080972</Xref>
-<Xref>PMID:12586941</Xref>
-<Note>the modification is observed when cyanide transfer to iron is blocked</Note>
-</ReferenceBlock>
-<Comment>This modification is produced naturally when the HypE protein undergoes an auto-catalyzed dehydration, using ATP, of its carboxy-terminal S-carbamoyl cysteine. See RESID:AA0332.</Comment>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>GO:0046892</Xref>
-<Xref>PSI-MOD:00338</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="mod_res__s-cyanocysteine__c">MOD_RES S-cyanocysteine</Feature>
-</Features>
-<Image src="/images/AA0333.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0333.PDB" />
-</Entry>
-<Entry id="AA0334">
-<Header>
-<Code>AA0334</Code>
-<Dates>
-<CreationDate>14-Mar-2003</CreationDate>
-<StrucRevDate>31-Dec-2013</StrucRevDate>
-<TextChngDate>31-Dec-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-cysteinyl hydrogenase diiron subcluster</Name>
-<AlternateName>1,7-biscarbonyl-1-(cystein-S-yl)-8-oxo-4-aza-2lambda(3),6 lambda(3)-dithia-1,7-diferratricyclo[4.2.0.0(2,7)]octane-1,7-dicarbonitrile</AlternateName>
-<SystematicName>mu-carbonyl-dicarbonyl-1kappaC,2kappaC-dicyanido-1kappaC,2kappaC-cysteinato-1kS-1,2-azadimethanthiol-1kS,2kS'-diiron</SystematicName>
-<Xref>PDBHET:HCN</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 10 Fe 2 H 9 N 4 O 4 S 3</Formula>
-<Weight type="chemical">457.08</Weight>
-<Weight type="physical">456.848468</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 7 Fe 2 H 4 N 3 O 3 S 2</Formula>
-<Weight type="chemical">353.94</Weight>
-<Weight type="physical">353.839283</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Peters, J.W.</Author>
-<Author>Lanzilotta, W.N.</Author>
-<Author>Lemon, B.J.</Author>
-<Author>Seefeldt, L.C.</Author>
-</Authors>
-<Citation>Science 282, 1853-1858, 1998</Citation>
-<Title>X-ray crystal structure of the Fe-only hydrogenase (CpI) from Clostridium pasteurianum to 1.8 angstrom resolution.</Title>
-<Xref>DOI:10.1126/science.282.5395.1853</Xref>
-<Xref>PMID:9836629</Xref>
-<Note>X-ray diffraction, 1.80 angstroms; a heterologous ligand containing sulfur is modeled</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Peters, J.W.</Author>
-<Author>Lanzilotta, W.N.</Author>
-<Author>Lemon, B.J.</Author>
-<Author>Seefeldt, L.C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, June 1993</Citation>
-<Description>Fe-only hydrogenase from Clostridium pasteurianum.</Description>
-<Xref>PDB:1FEH</Xref>
-<Note>X-ray diffraction, 1.80 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Nicolet, Y.</Author>
-<Author>Piras, C.</Author>
-<Author>Legrand, P.</Author>
-<Author>Hatchikian, C.E.</Author>
-<Author>Fontecilla-Camps, J.C.</Author>
-</Authors>
-<Citation>Structure 7, 13-23, 1999</Citation>
-<Title>Desulfovibrio desulfuricans iron hydrogenase: the structure shows unusual coordination to an active site Fe binuclear center.</Title>
-<Xref>PMID:10368269</Xref>
-<Note>X-ray diffraction, 1.60 angstroms; in the iron-only hydrogenase from a related species the heterologous group is modeled as propane-1,3-dithiol</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Nicolet, Y.</Author>
-<Author>Piras, C.</Author>
-<Author>Legrand, P.</Author>
-<Author>Hatchikian, C.E.</Author>
-<Author>Fontecilla-Camps, J.C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, November 1998</Citation>
-<Description>1.6 A resolution structure of the Fe-only hydrogenase from Desulfovibrio desulfuricans.</Description>
-<Xref>PDB:1HFE</Xref>
-<Note>X-ray diffraction, 1.60 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Pandey, A.S.</Author>
-<Author>Harris, T.V.</Author>
-<Author>Giles, L.J.</Author>
-<Author>Peters, J.W.</Author>
-<Author>Szilagyi, R.K.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 130, 4533-4540, 2008</Citation>
-<Title>Dithiomethylether as a ligand in the hydrogenase h-cluster.</Title>
-<Xref>DOI:10.1021/ja711187e</Xref>
-<Xref>PMID:18324814</Xref>
-<Note>X-ray diffraction, 1.39 angstroms; the heterologous group is modeled using density functional theory as oxydimethanethiol</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Pandey, A.S.</Author>
-<Author>Lemon, B.J.</Author>
-<Author>Peters, J.W.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, February 2008</Citation>
-<Description>1.39 Angstrom crystal structure of FE-only hydrogenase.</Description>
-<Xref>PDB:3C8Y</Xref>
-<Note>X-ray diffraction, 1.39 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Berggren, G.</Author>
-<Author>Adamska, A.</Author>
-<Author>Lambertz, C.</Author>
-<Author>Simmons, T.R.</Author>
-<Author>Esselborn, J.</Author>
-<Author>Atta, M.</Author>
-<Author>Gambarelli, S.</Author>
-<Author>Mouesca, J.M.</Author>
-<Author>Reijerse, E.</Author>
-<Author>Lubitz, W.</Author>
-<Author>Happe, T.</Author>
-<Author>Artero, V.</Author>
-<Author>Fontecave, M.</Author>
-</Authors>
-<Citation>Nature 499, 66-69, 2013</Citation>
-<Title>Biomimetic assembly and activation of [FeFe]-hydrogenases.</Title>
-<Xref>DOI:10.1038/nature12239</Xref>
-<Xref>PMID:23803769</Xref>
-<Note>determination of molecular structure by partial chemical synthesis of intermediates</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Esselborn, J.</Author>
-<Author>Lambertz, C.</Author>
-<Author>Adamska-Venkatesh, A.</Author>
-<Author>Simmons, T.</Author>
-<Author>Berggren, G.</Author>
-<Author>Noth, J.</Author>
-<Author>Siebel, J.</Author>
-<Author>Hemschemeier, A.</Author>
-<Author>Artero, V.</Author>
-<Author>Reijerse, E.</Author>
-<Author>Fontecave, M.</Author>
-<Author>Lubitz, W.</Author>
-<Author>Happe, T.</Author>
-</Authors>
-<Citation>Nature Chem. Biol. 9, 607-609, 2013</Citation>
-<Title>Spontaneous activation of [FeFe]-hydrogenases by an inorganic [2Fe] active site mimic.</Title>
-<Xref>DOI:10.1038/nchembio.1311</Xref>
-<Xref>PMID:23934246</Xref>
-<Note>a synthetic iron subcluster is incorporated and supports full enzyme activity</Note>
-</ReferenceBlock>
-<Comment>The structure of the metal cluster in this enzyme may vary in related organisms. The structure of the small heterologous ligand has been determined by incorporation of synthetic intermediates.</Comment>
-<Comment>Because of possible variations in the structure, a formal charge cannot be calculated.</Comment>
-<Comment>The cysteine sulfur is a mu(3) ligand that also ligates a 4Fe-4S cluster. For the metabolic source of the carbon monoxide and cyanide components of the cluster, see RESID:AA0332 and RESID:AA0333.</Comment>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Condition>incidental to RESID:AA0140</Condition>
-<Xref>GO:0046893</Xref>
-<Xref>PSI-MOD:00339</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>iron-sulfur protein</Keyword>
-<Keyword>metalloprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="metal__diiron subcluster__c">METAL Diiron subcluster</Feature>
-</Features>
-<Image src="/images/AA0334.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0334.PDB" />
-</Entry>
-<Entry id="AA0335">
-<Header>
-<Code>AA0335</Code>
-<Dates>
-<CreationDate>14-Mar-2003</CreationDate>
-<StrucRevDate>14-Mar-2003</StrucRevDate>
-<TextChngDate>31-Mar-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-amidino-L-cysteine</Name>
-<AlternateName>2-amino-3-amidinosulfanylpropanoic acid</AlternateName>
-<AlternateName>2-amino-3-amidinothiopropanoic acid</AlternateName>
-<AlternateName>alpha-amino-beta-amidinothiopropionic acid</AlternateName>
-<AlternateName>beta-(S-isothiourea)alanine</AlternateName>
-<AlternateName>beta-amidinothioalanine</AlternateName>
-<AlternateName>S-amidinocysteine</AlternateName>
-<SystematicName>(2R)-2-amino-3-(carbamimidoylsulfanyl)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 7 N 3 O 1 S 1</Formula>
-<Weight type="chemical">145.18</Weight>
-<Weight type="physical">145.030983</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 1 H 2 N 2 O 0 S 0</Formula>
-<Weight type="chemical">42.04</Weight>
-<Weight type="physical">42.021798</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Humm, A.</Author>
-<Author>Fritsche, E.</Author>
-<Author>Mann, K.</Author>
-<Author>Goehl, M.</Author>
-<Author>Huber, R.</Author>
-</Authors>
-<Citation>Biochem. J. 322, 771-776, 1997</Citation>
-<Title>Recombinant expression and isolation of human L-arginine:glycine amidinotransferase and identification of its active-site cysteine residue.</Title>
-<Xref>PMID:9148748</Xref>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>glycine amidinotransferase (EC 2.1.4.1)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>GO:0046894</Xref>
-<Xref>PSI-MOD:00340</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="act_site__amidino-cysteine intermediate__c">ACT_SITE Amidino-cysteine intermediate</Feature>
-</Features>
-<Image src="/images/AA0335.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0335.PDB" />
-</Entry>
-<Entry id="AA0336">
-<Header>
-<Code>AA0336</Code>
-<Dates>
-<CreationDate>14-Mar-2003</CreationDate>
-<StrucRevDate>14-Mar-2003</StrucRevDate>
-<TextChngDate>30-Jun-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-methyl-L-isoleucine</Name>
-<AlternateName>N-methylisoleucine</AlternateName>
-<SystematicName>(2S,3S)-2-methylamino-3-methylpentanoic acid</SystematicName>
-<Xref>CAS:4125-98-8</Xref>
-<Xref>PDBHET:IML</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 13 N 1 O 1</Formula>
-<Weight type="chemical">127.19</Weight>
-<Weight type="physical">127.099714</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0010">
-<Formula>C 1 H 2 N 0 O 0</Formula>
-<Weight type="chemical">14.03</Weight>
-<Weight type="physical">14.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Strom, M.S.</Author>
-<Author>Lory, S.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 266, 1656-1664, 1991</Citation>
-<Title>Amino acid substitutions in pilin of Pseudomonas aeruginosa. Effect on leader peptide cleavage, amino-terminal methylation, and pilus assembly.</Title>
-<Xref>PMID:1671038</Xref>
-<Note>the amino-terminal methyltransferase activity of prepilin peptidase is not specific for phenylalanine</Note>
-</ReferenceBlock>
-<Comment>This modification is predicted for proteins homologous to pilin in certain organisms where the position corresponding to N-methylphenylalanine instead encodes isoleucine.</Comment>
-<Comment>Polypeptides with monomethylated amino terminals can undergo premature cleavage during the coupling step of an Edman degradation. This can result in "preview" with both a residue and the following residue being seen from the first step on through a sequence.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>prepilin peptidase (EC 3.4.23.43)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>I</SequenceSpec>
-<Xref>GO:0046895</Xref>
-<Xref>PSI-MOD:00341</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>methylated amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n-methylisoleucine__i">MOD_RES N-methylisoleucine</Feature>
-</Features>
-<Image src="/images/AA0336.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0336.PDB" />
-</Entry>
-<Entry id="AA0337">
-<Header>
-<Code>AA0337</Code>
-<Dates>
-<CreationDate>14-Mar-2003</CreationDate>
-<StrucRevDate>14-Mar-2003</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-methyl-L-leucine</Name>
-<AlternateName>2-(methylamino)-4-methyl-valeric acid</AlternateName>
-<AlternateName>N-methylleucine</AlternateName>
-<SystematicName>(S)-2-methylamino-4-methylpentanoic acid</SystematicName>
-<Xref>CAS:3060-46-6</Xref>
-<Xref>PDBHET:MLE</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 13 N 1 O 1</Formula>
-<Weight type="chemical">127.19</Weight>
-<Weight type="physical">127.099714</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0011">
-<Formula>C 1 H 2 N 0 O 0</Formula>
-<Weight type="chemical">14.03</Weight>
-<Weight type="physical">14.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Strom, M.S.</Author>
-<Author>Lory, S.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 266, 1656-1664, 1991</Citation>
-<Title>Amino acid substitutions in pilin of Pseudomonas aeruginosa. Effect on leader peptide cleavage, amino-terminal methylation, and pilus assembly.</Title>
-<Xref>PMID:1671038</Xref>
-<Note>the amino-terminal methyltransferase activity of prepilin peptidase is not specific for phenylalanine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Armirotti, A.</Author>
-<Author>Damonte, G.</Author>
-<Author>Pozzolini, M.</Author>
-<Author>Mussino, F.</Author>
-<Author>Cerrano, C.</Author>
-<Author>Salis, A.</Author>
-<Author>Benatti, U.</Author>
-<Author>Giovine, M.</Author>
-</Authors>
-<Citation>J. Proteome Res. 8, 3995-4004, 2009</Citation>
-<Title>Primary structure and post-translational modifications of silicatein beta from the marine sponge Petrosia ficiformis (Poiret, 1789).</Title>
-<Xref>DOI:10.1021/pr900342y</Xref>
-<Xref>PMID:19522542</Xref>
-<Note>mass spectrometric identification; the authors do not provide numeric data to support their mass-spectrometric interpretations</Note>
-</ReferenceBlock>
-<Comment>This modification is predicted for proteins homologous to pilin in certain organisms where the position corresponding to N-methylphenylalanine instead encodes leucine.</Comment>
-<Comment>Polypeptides with monomethylated amino terminals can undergo premature cleavage during the coupling step of an Edman degradation. This can result in "preview" with both a residue and the following residue being seen from the first step on through a sequence.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>prepilin peptidase (EC 3.4.23.43)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>L</SequenceSpec>
-<Xref>GO:0046896</Xref>
-<Xref>PSI-MOD:00342</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>methylated amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n-methylleucine__l">MOD_RES N-methylleucine</Feature>
-</Features>
-<Image src="/images/AA0337.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0337.PDB" />
-</Entry>
-<Entry id="AA0338">
-<Header>
-<Code>AA0338</Code>
-<Dates>
-<CreationDate>14-Mar-2003</CreationDate>
-<StrucRevDate>14-Mar-2003</StrucRevDate>
-<TextChngDate>29-Oct-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-methyl-L-tyrosine</Name>
-<AlternateName>N-methyltyrosine</AlternateName>
-<SystematicName>(2S)-3-(4-hydroxyphenyl)-2-(methylamino)propanoic acid</SystematicName>
-<Xref>CAS:537-49-5</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 10 H 11 N 1 O 2</Formula>
-<Weight type="chemical">177.20</Weight>
-<Weight type="physical">177.078979</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0019">
-<Formula>C 1 H 2 N 0 O 0</Formula>
-<Weight type="chemical">14.03</Weight>
-<Weight type="physical">14.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Strom, M.S.</Author>
-<Author>Lory, S.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 266, 1656-1664, 1991</Citation>
-<Title>Amino acid substitutions in pilin of Pseudomonas aeruginosa. Effect on leader peptide cleavage, amino-terminal methylation, and pilus assembly.</Title>
-<Xref>PMID:1671038</Xref>
-<Note>the amino-terminal methyltransferase activity of prepilin peptidase is not specific for phenylalanine</Note>
-</ReferenceBlock>
-<Comment>This modification is predicted for proteins homologous to pilin in certain organisms where the position corresponding to N-methylphenylalanine instead encodes tyrosine.</Comment>
-<Comment>Polypeptides with monomethylated amino terminals can undergo premature cleavage during the coupling step of an Edman degradation. This can result in "preview" with both a residue and the following residue being seen from the first step on through a sequence.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>prepilin peptidase (EC 3.4.23.43)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>Y</SequenceSpec>
-<Xref>GO:0046897</Xref>
-<Xref>PSI-MOD:00343</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>methylated amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n-methyltyrosine__y">MOD_RES N-methyltyrosine</Feature>
-</Features>
-<Image src="/images/AA0338.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0338.PDB" />
-</Entry>
-<Entry id="AA0339">
-<Header>
-<Code>AA0339</Code>
-<Dates>
-<CreationDate>25-Apr-2003</CreationDate>
-<StrucRevDate>25-Apr-2003</StrucRevDate>
-<TextChngDate>30-Sep-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-palmitoyl-glycine</Name>
-<AlternateName>(hexadecanamido)acetic acid</AlternateName>
-<AlternateName>(hexadecanoylamino)acetic acid</AlternateName>
-<AlternateName>N-(1-oxohexadecyl)glycine</AlternateName>
-<SystematicName>(hexadecanoylamino)ethanoic acid</SystematicName>
-<Xref>CAS:2441-41-0</Xref>
-<Xref>PDBHET:140</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 18 H 34 N 1 O 2</Formula>
-<Weight type="chemical">296.47</Weight>
-<Weight type="physical">296.258954</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0008">
-<Formula>C 16 H 30 N 0 O 1 S 0</Formula>
-<Weight type="chemical">238.41</Weight>
-<Weight type="physical">238.229666</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kleuss, C.</Author>
-<Author>Krause, E.</Author>
-</Authors>
-<Citation>EMBO J. 22, 826-832, 2003</Citation>
-<Title>Galpha(s) is palmitoylated at the N-terminal glycine.</Title>
-<Xref>DOI:10.1093/emboj/cdg095</Xref>
-<Xref>PMID:12574119</Xref>
-<Note>mass spectrometric characterization</Note>
-</ReferenceBlock>
-<Comment>This modification should not be confused with N-myristoyl-glycine (see RESID:AA0059).</Comment>
-<GeneratingEnzyme>
-<EnzymeName>glycylpeptide N-palmitoyltransferase (EC 2.3.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>G</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Condition>incidental to RESID:AA0060</Condition>
-<Xref>GO:0046918</Xref>
-<Xref>PSI-MOD:00344</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-<Keyword>lipoprotein</Keyword>
-<Keyword>palmitoylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__n-palmitoyl glycine__g">LIPID N-palmitoyl glycine</Feature>
-</Features>
-<Image src="/images/AA0339.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0339.PDB" />
-</Entry>
-<Entry id="AA0340">
-<Header>
-<Code>AA0340</Code>
-<Dates>
-<CreationDate>09-May-2003</CreationDate>
-<StrucRevDate>09-May-2003</StrucRevDate>
-<TextChngDate>31-Mar-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>2-(L-cystein-S-yl)-L-phenylalanine</Name>
-<AlternateName>(2R,5R)-2,5-diamino-3-thia-2-phenylmethylhexanedioic acid</AlternateName>
-<AlternateName>alpha-(L-cystein-S-yl)-L-phenylalanine</AlternateName>
-<SystematicName>(2R)-2-amino-2-[(2R)-2-amino-2-carboxyethyl]sulfanyl-3-phenylpropanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 12 H 12 N 2 O 2 S 1</Formula>
-<Weight type="chemical">248.30</Weight>
-<Weight type="physical">248.061949</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0014">
-<Formula>C 0 H -2 N 0 O 0 S 0</Formula>
-<Weight type="chemical">-2.02</Weight>
-<Weight type="physical">-2.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Babasaki, K.</Author>
-<Author>Takao, T.</Author>
-<Author>Shimonishi, Y.</Author>
-<Author>Kurahashi, K.</Author>
-</Authors>
-<Citation>J. Biochem. 98, 585-603, 1985</Citation>
-<Title>Subtilosin A, a new antibiotic peptide produced by Bacillus subtilis 168: isolation, structural analysis, and biogenesis.</Title>
-<Xref>PMID:3936839</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kawulka, K.</Author>
-<Author>Sprules, T.</Author>
-<Author>McKay, R.T.</Author>
-<Author>Mercier, P.</Author>
-<Author>Diaper, C.M.</Author>
-<Author>Zuber, P.</Author>
-<Author>Vederas, J.C.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 125, 4726-4727, 2003</Citation>
-<Title>Structure of subtilosin A, an antimicrobial peptide from Bacillus subtilis with unusual posttranslational modifications linking cysteine sulfurs to alpha-carbons of phenylalanine and threonine.</Title>
-<Xref>DOI:10.1021/ja029654t</Xref>
-<Xref>PMID:12696888</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kawulka, K.E.</Author>
-<Author>Sprules, T.</Author>
-<Author>Diaper, C.M.</Author>
-<Author>Whittal, R.M.</Author>
-<Author>McKay, R.T.</Author>
-<Author>Mercier, P.</Author>
-<Author>Zuber, P.</Author>
-<Author>Vederas, J.C.</Author>
-</Authors>
-<Citation>Biochemistry 43, 3385-3395, 2004</Citation>
-<Title>Structure of subtilosin A, a cyclic antimicrobial peptide from Bacillus subtilis with unusual sulfur to alpha-carbon cross-links: formation and reduction of alpha-thio-alpha-amino acid derivatives.</Title>
-<Xref>DOI:10.1021/bi0359527</Xref>
-<Xref>PMID:15035610</Xref>
-<Note>mass spectrometric, (1)H-NMR, (13)C-NMR and (15)N-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kawulka, K.E.</Author>
-<Author>Sprules, T.</Author>
-<Author>McKay, R.T.</Author>
-<Author>Mercier, P.</Author>
-<Author>Diaper, C.M.</Author>
-<Author>Zuber, P.</Author>
-<Author>Vederas, J.C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, July 2003</Citation>
-<Description>Structure of subtilosin A.</Description>
-<Xref>PDB:1PXQ</Xref>
-<Note>conformation by (1)H-NMR, (13)C-NMR and (15)N-NMR</Note>
-</ReferenceBlock>
-<Comment>The L-stereoisomer of the 2-S-cysteinyl substituted phenylalanine has R configuration.</Comment>
-<SequenceCode>
-<SequenceSpec>C, F</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>GO:0046924</Xref>
-<Xref>PSI-MOD:00345</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__2-cysteinyl-l-phenylalanine (cys-phe)__c__f">CROSSLNK 2-cysteinyl-L-phenylalanine (Cys-Phe)</Feature>
-</Features>
-<Image src="/images/AA0340.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0340.PDB" />
-</Entry>
-<Entry id="AA0341">
-<Header>
-<Code>AA0341</Code>
-<Dates>
-<CreationDate>09-May-2003</CreationDate>
-<StrucRevDate>09-May-2003</StrucRevDate>
-<TextChngDate>20-May-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>2-(L-cystein-S-yl)-D-phenylalanine</Name>
-<AlternateName>(2S,5R)-2,5-diamino-3-thia-2-phenylmethylhexanedioic acid</AlternateName>
-<AlternateName>alpha-(L-cystein-S-yl)-D-phenylalanine</AlternateName>
-<SystematicName>(2S)-2-amino-2-[(2R)-2-amino-2-carboxyethyl]sulfanyl-3-phenylpropanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 12 H 12 N 2 O 2 S 1</Formula>
-<Weight type="chemical">248.30</Weight>
-<Weight type="physical">248.061949</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0014">
-<Formula>C 0 H -2 N 0 O 0 S 0</Formula>
-<Weight type="chemical">-2.02</Weight>
-<Weight type="physical">-2.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Babasaki, K.</Author>
-<Author>Takao, T.</Author>
-<Author>Shimonishi, Y.</Author>
-<Author>Kurahashi, K.</Author>
-</Authors>
-<Citation>J. Biochem. 98, 585-603, 1985</Citation>
-<Title>Subtilosin A, a new antibiotic peptide produced by Bacillus subtilis 168: isolation, structural analysis, and biogenesis.</Title>
-<Xref>PMID:3936839</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kawulka, K.</Author>
-<Author>Sprules, T.</Author>
-<Author>McKay, R.T.</Author>
-<Author>Mercier, P.</Author>
-<Author>Diaper, C.M.</Author>
-<Author>Zuber, P.</Author>
-<Author>Vederas, J.C.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 125, 4726-4727, 2003</Citation>
-<Title>Structure of subtilosin A, an antimicrobial peptide from Bacillus subtilis with unusual posttranslational modifications linking cysteine sulfurs to alpha-carbons of phenylalanine and threonine.</Title>
-<Xref>DOI:10.1021/ja029654t</Xref>
-<Xref>PMID:12696888</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kawulka, K.E.</Author>
-<Author>Sprules, T.</Author>
-<Author>Diaper, C.M.</Author>
-<Author>Whittal, R.M.</Author>
-<Author>McKay, R.T.</Author>
-<Author>Mercier, P.</Author>
-<Author>Zuber, P.</Author>
-<Author>Vederas, J.C.</Author>
-</Authors>
-<Citation>Biochemistry 43, 3385-3395, 2004</Citation>
-<Title>Structure of subtilosin A, a cyclic antimicrobial peptide from Bacillus subtilis with unusual sulfur to alpha-carbon cross-links: formation and reduction of alpha-thio-alpha-amino acid derivatives.</Title>
-<Xref>DOI:10.1021/bi0359527</Xref>
-<Xref>PMID:15035610</Xref>
-<Note>mass spectrometric, (1)H-NMR, (13)C-NMR and (15)N-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kawulka, K.E.</Author>
-<Author>Sprules, T.</Author>
-<Author>McKay, R.T.</Author>
-<Author>Mercier, P.</Author>
-<Author>Diaper, C.M.</Author>
-<Author>Zuber, P.</Author>
-<Author>Vederas, J.C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, July 2003</Citation>
-<Description>Structure of subtilosin A.</Description>
-<Xref>PDB:1PXQ</Xref>
-<Note>conformation by (1)H-NMR, (13)C-NMR and (15)N-NMR</Note>
-</ReferenceBlock>
-<Comment>The D-stereoisomer of the 2-S-cysteinyl substituted phenylalanine has S configuration.</Comment>
-<SequenceCode>
-<SequenceSpec>C, F</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>GO:0046925</Xref>
-<Xref>PSI-MOD:00346</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>D-amino acid</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__2-cysteinyl-d-phenylalanine (cys-phe)__c__f">CROSSLNK 2-cysteinyl-D-phenylalanine (Cys-Phe)</Feature>
-</Features>
-<Image src="/images/AA0341.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0341.PDB" />
-</Entry>
-<Entry id="AA0342">
-<Header>
-<Code>AA0342</Code>
-<Dates>
-<CreationDate>09-May-2003</CreationDate>
-<StrucRevDate>09-May-2003</StrucRevDate>
-<TextChngDate>31-Dec-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>2-(L-cystein-S-yl)-D-allo-threonine</Name>
-<AlternateName>(2R,5S,6R)-2,5-diamino-5-carboxy-6-hydroxy-4-thiaheptanoic acid</AlternateName>
-<AlternateName>alpha-(L-cystein-S-yl)-D-allo-threonine</AlternateName>
-<SystematicName>(2S,3R)-2-amino-2-[(2R)-2-amino-2-carboxyethyl]sulfanyl-3-hydroxybutanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 10 N 2 O 3 S 1</Formula>
-<Weight type="chemical">202.23</Weight>
-<Weight type="physical">202.041213</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0017">
-<Formula>C 0 H -2 N 0 O 0 S 0</Formula>
-<Weight type="chemical">-2.02</Weight>
-<Weight type="physical">-2.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Babasaki, K.</Author>
-<Author>Takao, T.</Author>
-<Author>Shimonishi, Y.</Author>
-<Author>Kurahashi, K.</Author>
-</Authors>
-<Citation>J. Biochem. 98, 585-603, 1985</Citation>
-<Title>Subtilosin A, a new antibiotic peptide produced by Bacillus subtilis 168: isolation, structural analysis, and biogenesis.</Title>
-<Xref>PMID:3936839</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kawulka, K.</Author>
-<Author>Sprules, T.</Author>
-<Author>McKay, R.T.</Author>
-<Author>Mercier, P.</Author>
-<Author>Diaper, C.M.</Author>
-<Author>Zuber, P.</Author>
-<Author>Vederas, J.C.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 125, 4726-4727, 2003</Citation>
-<Title>Structure of subtilosin A, an antimicrobial peptide from Bacillus subtilis with unusual posttranslational modifications linking cysteine sulfurs to alpha-carbons of phenylalanine and threonine.</Title>
-<Xref>DOI:10.1021/ja029654t</Xref>
-<Xref>PMID:12696888</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kawulka, K.E.</Author>
-<Author>Sprules, T.</Author>
-<Author>Diaper, C.M.</Author>
-<Author>Whittal, R.M.</Author>
-<Author>McKay, R.T.</Author>
-<Author>Mercier, P.</Author>
-<Author>Zuber, P.</Author>
-<Author>Vederas, J.C.</Author>
-</Authors>
-<Citation>Biochemistry 43, 3385-3395, 2004</Citation>
-<Title>Structure of subtilosin A, a cyclic antimicrobial peptide from Bacillus subtilis with unusual sulfur to alpha-carbon cross-links: formation and reduction of alpha-thio-alpha-amino acid derivatives.</Title>
-<Xref>DOI:10.1021/bi0359527</Xref>
-<Xref>PMID:15035610</Xref>
-<Note>mass spectrometric, (1)H-NMR, (13)C-NMR and (15)N-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kawulka, K.E.</Author>
-<Author>Sprules, T.</Author>
-<Author>McKay, R.T.</Author>
-<Author>Mercier, P.</Author>
-<Author>Diaper, C.M.</Author>
-<Author>Zuber, P.</Author>
-<Author>Vederas, J.C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, July 2003</Citation>
-<Description>Structure of subtilosin A.</Description>
-<Xref>PDB:1PXQ</Xref>
-<Note>(1)H-NMR, (13)C-NMR and (15)N-NMR geometry constraint modeling; stereochemical determination</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sit, C.S.</Author>
-<Author>van Belkum, M.J.</Author>
-<Author>McKay, R.T.</Author>
-<Author>Worobo, R.W.</Author>
-<Author>Vederas, J.C.</Author>
-</Authors>
-<Citation>Angew. Chem. Int. Ed. Engl. 50, 8718-8721, 2011</Citation>
-<Title>The 3D solution structure of thurincin H, a bacteriocin with four sulfur to α-carbon crosslinks.</Title>
-<Xref>DOI:10.1002/anie.201102527</Xref>
-<Xref>PMID:21786372</Xref>
-<Note>mass spectrometric, (1)H-NMR, (13)C-NMR and (15)N-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sit, C.S.</Author>
-<Author>van Belkum, M.J.</Author>
-<Author>McKay, R.T.</Author>
-<Author>Worobo, R.W.</Author>
-<Author>Vederas, J.C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, April 2011</Citation>
-<Description>Thurincin H.</Description>
-<Xref>PDB:2LBZ</Xref>
-<Note>(1)H-NMR, (13)C-NMR and (15)N-NMR geometry constraint modeling; stereochemical determination</Note>
-</ReferenceBlock>
-<Comment>The D-stereoisomer of the 2-S-cysteinyl substituted threonine has S configuration. The second chiral center of the threonine is not inverted from the L-threo diastereomer (J.C. Vederas, private communication, 2003), and is thus D-allo.</Comment>
-<SequenceCode>
-<SequenceSpec>C, T</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>GO:0046926</Xref>
-<Xref>PSI-MOD:00347</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>D-amino acid</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__2-cysteinyl-d-allo-threonine (cys-thr)__c__t">CROSSLNK 2-cysteinyl-D-allo-threonine (Cys-Thr)</Feature>
-</Features>
-<Image src="/images/AA0342.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0342.PDB" />
-</Entry>
-<Entry id="AA0343">
-<Header>
-<Code>AA0343</Code>
-<Dates>
-<CreationDate>30-May-2003</CreationDate>
-<StrucRevDate>30-May-2003</StrucRevDate>
-<TextChngDate>31-Dec-2008</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-carbamoyl-L-alanine</Name>
-<AlternateName>2-ureidopropanoic acid</AlternateName>
-<AlternateName>N-carbamylalanine</AlternateName>
-<SystematicName>(S)-2-(carbamoylamino)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 7 N 2 O 2</Formula>
-<Weight type="chemical">115.11</Weight>
-<Weight type="physical">115.050752</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0001">
-<Formula>C 1 H 1 N 1 O 1</Formula>
-<Weight type="chemical">43.02</Weight>
-<Weight type="physical">43.005814</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Van Driessche, G.</Author>
-<Author>Vandenberghe, I.</Author>
-<Author>Jacquemotte, F.</Author>
-<Author>Devreese, B.</Author>
-<Author>Van Beeumen, J.J.</Author>
-</Authors>
-<Citation>J. Mass Spectrom. 37, 858-866, 2002</Citation>
-<Title>Mass spectrometric identification of in vivo carbamylation of the amino terminus of Ectothiorhodospira mobilis high-potential iron-sulfur protein, isozyme 1.</Title>
-<Xref>DOI:10.1002/jms.348</Xref>
-<Xref>PMID:12203680</Xref>
-<Note>an apparently natural alpha-amino carbamoylation; mass spectrometric detection and characterization by collision-induced dissociation (CID) MS/MS; identification by synthesis</Note>
-</ReferenceBlock>
-<Comment>Carbamoylation of the alpha-amino group can be artifactual, especially when urea buffers are used.</Comment>
-<SequenceCode>
-<SequenceSpec>A</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0046945</Xref>
-<Xref>PSI-MOD:00348</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n-carbamoylalanine__a">MOD_RES N-carbamoylalanine</Feature>
-</Features>
-<Image src="/images/AA0343.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0343.PDB" />
-</Entry>
-<Entry id="AA0344">
-<Header>
-<Code>AA0344</Code>
-<Dates>
-<CreationDate>30-Jun-2003</CreationDate>
-<StrucRevDate>30-Jun-2003</StrucRevDate>
-<TextChngDate>30-Jun-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N,N-(L-cysteine-1,S-diyl)-L-serine</Name>
-<AlternateName>2-(4-amino-3-oxo-isothiazolidin-2-yl)-3-hydroxy-propanoic acid</AlternateName>
-<AlternateName>4-amino-3-isothiazolidinone-L-serine</AlternateName>
-<AlternateName>serine-cysteine sulfenyl amide cross-link</AlternateName>
-<AlternateName>serine-cysteine sulphenyl amide cross-link</AlternateName>
-<SystematicName>(2S)-2-[(4R)-4-amino-3-oxo-1,2-thiazolidin-2-yl]-3-hydroxypropanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 8 N 2 O 3 S 1</Formula>
-<Weight type="chemical">188.20</Weight>
-<Weight type="physical">188.025563</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0016">
-<Formula>C 0 H -2 N 0 O 0 S 0</Formula>
-<Weight type="chemical">-2.02</Weight>
-<Weight type="physical">-2.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Salmeen, A.</Author>
-<Author>Andersen, J.N.</Author>
-<Author>Myers, M.P.</Author>
-<Author>Meng, T.C.</Author>
-<Author>Hinks, J.A.</Author>
-<Author>Tonks, N.K.</Author>
-<Author>Barford, D.</Author>
-</Authors>
-<Citation>Nature 423, 769-773, 2003</Citation>
-<Title>Redox regulation of protein tyrosine phosphatase 1B involves a sulphenyl-amide intermediate.</Title>
-<Xref>DOI:10.1038/nature01680</Xref>
-<Xref>PMID:12802338</Xref>
-<Note>X-ray diffraction, 1.8 angstroms; (18)O labeling; mass spectrometric identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Salmeen, A.</Author>
-<Author>Andersen, J.N.</Author>
-<Author>Myers, M.P.</Author>
-<Author>Meng, T.C.</Author>
-<Author>Hinks, J.A.</Author>
-<Author>Tonks, N.K.</Author>
-<Author>Barford, D.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, March 2003</Citation>
-<Description>PTP1B with the catalytic cysteine oxidized to a sulfenyl-amide bond.</Description>
-<Xref>PDB:1OEM</Xref>
-<Note>X-ray diffraction, 1.8 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>van Montfort, R.L.M.</Author>
-<Author>Congreve, M.</Author>
-<Author>Tisi, D.</Author>
-<Author>Carr, R.</Author>
-<Author>Jhoti, H.</Author>
-</Authors>
-<Citation>Nature 423, 773-777, 2003</Citation>
-<Title>Oxidation state of the active-site cysteine in protein tyrosine phosphatase 1B.</Title>
-<Xref>DOI:10.1038/nature01681</Xref>
-<Xref>PMID:12802339</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>van Montfort, R.L.M.</Author>
-<Author>Congreve, M.</Author>
-<Author>Tisi, D.</Author>
-<Author>Carr, R.</Author>
-<Author>Jhoti, H.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, March 2003</Citation>
-<Description>Oxidation state of protein tyrosine phosphatase 1B.</Description>
-<Xref>PDB:1OES</Xref>
-<Note>X-ray diffraction, 2.2 angstroms</Note>
-</ReferenceBlock>
-<Comment>This cross-link is formed by the condensation of a cysteine sulfenic acid with the alpha-amido of the following residue. It can apparently be reversed by simple disulfhydryl reduction under physiological conditions.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C, S</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Xref>GO:0048109</Xref>
-<Xref>PSI-MOD:00349</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>isothiazole ring</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__n,n-(cysteine-1,s-diyl)serine (cys-ser)__c__s">CROSSLNK N,N-(cysteine-1,S-diyl)serine (Cys-Ser)</Feature>
-</Features>
-<Image src="/images/AA0344.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0344.PDB" />
-</Entry>
-<Entry id="AA0345">
-<Header>
-<Code>AA0345</Code>
-<Dates>
-<CreationDate>05-Sep-2003</CreationDate>
-<StrucRevDate>05-Sep-2003</StrucRevDate>
-<TextChngDate>30-Apr-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-threonyl-pentaglycyl-murein peptidoglycan</Name>
-<AlternateName>(2R,6S)-2-(N-mureinyl-(R)-alanyl-(S)-isoglutamyl)amino-6-(threonyl-pentaglycyl)amino-pimeloyl-(S)-alanyl-(S)-alanine</AlternateName>
-</Names>
-<FormulaBlock>
-<Formula>C 14 H 22 N 6 O 7 +</Formula>
-<Weight type="chemical">386.37 +</Weight>
-<Weight type="physical">386.154997 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0017">
-<Formula>C 10 H 14 N 5 O 4 +</Formula>
-<Weight type="chemical">268.25 +</Weight>
-<Weight type="physical">268.104579 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Schneewind, O.</Author>
-<Author>Model, P.</Author>
-<Author>Fischetti, V.A.</Author>
-</Authors>
-<Citation>Cell 70, 267-281, 1992</Citation>
-<Title>Sorting of protein A to the staphylococcal cell wall.</Title>
-<Xref>DOI:10.1016/0092-8674(92)90101-H</Xref>
-<Xref>PMID:1638631</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Novick, R.P.</Author>
-</Authors>
-<Citation>Trends Microbiol. 8, 148-151, 2000</Citation>
-<Title>Sortase: the surface protein anchoring transpeptidase and the LPXTG motif.</Title>
-<Xref>DOI:10.1016/S0966-842X(00)01741-8</Xref>
-<Xref>PMID:10754567</Xref>
-<Note>review</Note>
-</ReferenceBlock>
-<Comment>Some bacterial proteins containing the sequence motif LPXTG are covalently attached to the cell wall murein. These proteins are cleaved after the threonine and transacylated to a pentaglycyl "crossbridge" peptide attached to the 6(D)-amino of meso-2,6-diaminopimelic acid in the murein peptidoglycan. In some gram-positive bacteria the meso-2,6-diaminopimelic acid is replaced by L-lysine. The form with meso-2,6-diaminopimelic acid is shown.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>sortase aminoacyltransferase (EC 2.3.2.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>T</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0042902</Xref>
-<Xref>PSI-MOD:00350</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>glycoprotein</Keyword>
-<Keyword>peptidoglycan</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__pentaglycyl murein peptidoglycan amidated threonine__t ">MOD_RES Pentaglycyl murein peptidoglycan amidated threonine</Feature>
-</Features>
-<Image src="/images/AA0345.GIF" alt="DUMMY.GIF" />
-</Entry>
-<Entry id="AA0346">
-<Header>
-<Code>AA0346</Code>
-<Dates>
-<CreationDate>30-Sep-2003</CreationDate>
-<StrucRevDate>30-Sep-2003</StrucRevDate>
-<TextChngDate>31-Mar-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-glycyl-1-(phosphatidyl)ethanolamine</Name>
-<AlternateName>N-glycyl-1-palmitoyl-2-oleoyl-sn-glycero-3-phosphoethanolamine</AlternateName>
-<SystematicName>(R)-1-hexadecanoyloxy-2-((Z)-9-octadecenoyloxy)-3-[2-(aminoacetylamino)ethyloxyphospho]propane</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 41 H 78 N 2 O 9 P 1 +</Formula>
-<Weight type="chemical">774.05 +</Weight>
-<Weight type="physical">773.544494 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0008">
-<Formula>C 39 H 74 N 1 O 7 P 1 +</Formula>
-<Weight type="chemical">699.99 +</Weight>
-<Weight type="physical">699.520290 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ichimura, Y.</Author>
-<Author>Kirisako, T.</Author>
-<Author>Takao, T.</Author>
-<Author>Satomi, Y.</Author>
-<Author>Shimonishi, Y.</Author>
-<Author>Ishihara, N.</Author>
-<Author>Mizushima, N.</Author>
-<Author>Tanida, I.</Author>
-<Author>Kominami, E.</Author>
-<Author>Ohsumi, M.</Author>
-<Author>Noda, T.</Author>
-<Author>Ohsumi, Y.</Author>
-</Authors>
-<Citation>Nature 408, 488-492, 2000</Citation>
-<Title>A ubiquitin-like system mediates protein lipidation.</Title>
-<Xref>DOI:10.1038/35044114</Xref>
-<Xref>PMID:11100732</Xref>
-</ReferenceBlock>
-<Comment>A representative phospholipid structure is shown.</Comment>
-<Comment>Cleavage of a carboxyl terminal propeptide accompanies transamidation.</Comment>
-<SequenceCode>
-<SequenceSpec>G</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0050495</Xref>
-<Xref>PSI-MOD:00351</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>lipoprotein</Keyword>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__phosphatidylethanolamine amidated glycine__g">LIPID Phosphatidylethanolamine amidated glycine</Feature>
-</Features>
-<Image src="/images/AA0346.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0346.PDB" />
-</Entry>
-<Entry id="AA0347">
-<Header>
-<Code>AA0347</Code>
-<Dates>
-<CreationDate>30-Sep-2003</CreationDate>
-<StrucRevDate>30-Sep-2003</StrucRevDate>
-<TextChngDate>29-Jan-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-glutamyl 5-omega-hydroxyceramide ester</Name>
-<AlternateName>2-[30-(isoglutamyloxy)triacontanoyl]icosasphingosine</AlternateName>
-<SystematicName>(S)-2-amino-5-[30-((2S,3R,4E)-1,3-dihydroxyicos-4-en-2-ylamino)-30-oxotriacontan-1-yloxy]-5-oxopentanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 55 H 104 N 2 O 6 +</Formula>
-<Weight type="chemical">889.44 +</Weight>
-<Weight type="physical">888.789439 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0007">
-<Formula>C 50 H 96 N 0 O 4 +</Formula>
-<Weight type="chemical">761.31 +</Weight>
-<Weight type="physical">760.730862 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Marekov, L.N.</Author>
-<Author>Steinert, P.M.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 273, 17763-17770, 1998</Citation>
-<Title>Ceramides are bound to structural proteins of the human foreskin epidermal cornified cell envelope.</Title>
-<Xref>DOI:10.1074/jbc.273.28.17763</Xref>
-<Xref>PMID:9651377</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Nemes, Z.</Author>
-<Author>Marekov, L.N.</Author>
-<Author>Fesus, L.</Author>
-<Author>Steinert, P.M.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 96, 8402-8407, 1999</Citation>
-<Title>A novel function for transglutaminase 1: attachment of long-chain omega-hydroxyceramides to involucrin by ester bond formation.</Title>
-<Xref>DOI:10.1073/pnas.96.15.8402</Xref>
-<Xref>PMID:10411887</Xref>
-</ReferenceBlock>
-<Comment>This lipid modification is thought to span the lipid bilayer.</Comment>
-<Comment>A representative structure is shown.</Comment>
-<SequenceCode>
-<SequenceSpec>Q</SequenceSpec>
-<Xref>GO:0050496</Xref>
-<Xref>PSI-MOD:00352</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lipoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__omega-hydroxyceramide glutamate ester__q">LIPID Omega-hydroxyceramide glutamate ester</Feature>
-</Features>
-<Image src="/images/AA0347.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0347.PDB" />
-</Entry>
-<Entry id="AA0348">
-<Header>
-<Code>AA0348</Code>
-<Dates>
-<CreationDate>31-Oct-2003</CreationDate>
-<StrucRevDate>31-Oct-2003</StrucRevDate>
-<TextChngDate>31-Dec-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-[5'-(L-tryptoph-6'-yl)-L-tyrosin-3'-yl]-L-methionin-S-ium</Name>
-<AlternateName>5'-(6'-tryptophyl)-tyrosin-3'-yl-methionin-S-ium</AlternateName>
-</Names>
-<FormulaBlock>
-<Formula>C 25 H 25 N 4 O 4 S 1</Formula>
-<FormalCharge>1+</FormalCharge>
-<Weight type="chemical">477.56</Weight>
-<Weight type="physical">477.159103</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0013 AA0018 AA0019">
-<Formula>C 0 H -3 N 0 O 0 S 0</Formula>
-<FormalCharge>1+</FormalCharge>
-<Weight type="chemical">-3.02</Weight>
-<Weight type="physical">-3.024024</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yamada, Y.</Author>
-<Author>Fujiwara, T.</Author>
-<Author>Sato, T.</Author>
-<Author>Igarashi, N.</Author>
-<Author>Tanaka, N.</Author>
-</Authors>
-<Citation>Nature Struct. Biol. 9, 691-695, 2002</Citation>
-<Title>The 2.0 A crystal structure of catalase-peroxidase from Haloarcula marismortui.</Title>
-<Xref>DOI:10.1038/nsb834</Xref>
-<Xref>PMID:12172540</Xref>
-<Note>X-ray diffraction, 2.0 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yamada, Y.</Author>
-<Author>Fujiwara, T.</Author>
-<Author>Sato, T.</Author>
-<Author>Igarashi, N.</Author>
-<Author>Tanaka, N.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, January 2002</Citation>
-<Description>Crystal structure of catalase-peroxidase from Haloarcula marismortui.</Description>
-<Xref>PDB:1ITK</Xref>
-<Note>X-ray diffraction, 2.0 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ghiladi, R.A.</Author>
-<Author>Medzihradszky, K.F.</Author>
-<Author>Ortiz de Montellano, P.R.</Author>
-</Authors>
-<Citation>Biochemistry 44, 15093-15105, 2005</Citation>
-<Title>Role of the Met-Tyr-Trp cross-link in Mycobacterium tuberculosis catalase-peroxidase (KatG) as revealed by KatG(M255I).</Title>
-<Xref>DOI:10.1021/bi051463q</Xref>
-<Xref>PMID:16285713</Xref>
-<Note>chemical characterization; directed mutation analysis</Note>
-</ReferenceBlock>
-<Comment>This modification is produced auto-catalytically.</Comment>
-<SequenceCode>
-<SequenceSpec>M, W, Y</SequenceSpec>
-<Condition>cross-link 3</Condition>
-<Xref>GO:0050739</Xref>
-<Xref>PSI-MOD:00353</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="crosslnk__tryptophyl-tyrosyl-methioninium (trp-tyr) (with m-__w__y">CROSSLNK Tryptophyl-tyrosyl-methioninium (Trp-Tyr) (with M-...)</Feature>
-<Feature type="UniProt" key="crosslnk__tryptophyl-tyrosyl-methioninium (tyr-met) (with w-__y__m">CROSSLNK Tryptophyl-tyrosyl-methioninium (Tyr-Met) (with W-...)</Feature>
-</Features>
-<Image src="/images/AA0348.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0348.PDB" />
-</Entry>
-<Entry id="AA0349">
-<Header>
-<Code>AA0349</Code>
-<Dates>
-<CreationDate>31-Oct-2003</CreationDate>
-<StrucRevDate>31-Oct-2003</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-(riboflavin phosphoryl)-L-threonine</Name>
-<AlternateName>O3-threonyl flavin mononucleotide</AlternateName>
-<AlternateName>O3-threonyl FMN</AlternateName>
-<SystematicName>(2S,3R)-2-amino-3-(riboflavin 5'-hydrogen phosphonoxy)butanoic acid</SystematicName>
-<Xref>ChEBI:74346</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 21 H 26 N 5 O 10 P 1</Formula>
-<Weight type="chemical">539.44</Weight>
-<Weight type="physical">539.141729</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0017">
-<Formula>C 17 H 19 N 4 O 8 P 1</Formula>
-<Weight type="chemical">438.33</Weight>
-<Weight type="physical">438.094050</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Zhou, W.</Author>
-<Author>Bertsova, Y.V.</Author>
-<Author>Feng, B.</Author>
-<Author>Tsatsos, P.</Author>
-<Author>Verkhovskaya, M.L.</Author>
-<Author>Gennis, R.B.</Author>
-<Author>Bogachev, A.V.</Author>
-<Author>Barquera, B.</Author>
-</Authors>
-<Citation>Biochemistry 38, 16246-16252, 1999</Citation>
-<Title>Sequencing and preliminary characterization of the Na+-translocating NADH:ubiquinone oxidoreductase from Vibrio harveyi.</Title>
-<Xref>DOI:10.1021/bi991664s</Xref>
-<Xref>PMID:10587447</Xref>
-<Note>original identification as 1'-(8alpha-FMN)-histidine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hayashi, M.</Author>
-<Author>Nakayama, Y.</Author>
-<Author>Yasui, M.</Author>
-<Author>Maeda, M.</Author>
-<Author>Furuishi, K.</Author>
-<Author>Unemoto, T.</Author>
-</Authors>
-<Citation>FEBS Lett. 488, 5-8, 2001</Citation>
-<Title>FMN is covalently attached to a threonine residue in the NqrB and NqrC subunits of Na(+)-translocating NADH-quinone reductase from Vibrio alginolyticus.</Title>
-<Xref>DOI:10.1016/S0014-5793(00)02404-2</Xref>
-<Xref>PMID:11163785</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Barquera, B.</Author>
-<Author>Haese, C.C.</Author>
-<Author>Gennis, R.B.</Author>
-</Authors>
-<Citation>FEBS Lett. 492, 45-49, 2001</Citation>
-<Title>Expression and mutagenesis of the NqrC subunit of the NQR respiratory Na(+) pump from Vibrio cholerae with covalently attached FMN.</Title>
-<Xref>DOI:10.1016/S0014-5793(01)02224-4</Xref>
-<Xref>PMID:11248234</Xref>
-<Note>cloning and expression of the gene in Escherichia coli results in the production of an unmodified protein, which may indicate that an enzyme required for this modification is not present</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Backiel, J.</Author>
-<Author>Juárez, O.</Author>
-<Author>Zagorevski, D.V.</Author>
-<Author>Wang, Z.</Author>
-<Author>Nilges, M.J.</Author>
-<Author>Barquera, B.</Author>
-</Authors>
-<Citation>Biochemistry 47, 11273-11284, 2008</Citation>
-<Title>Covalent binding of flavins to RnfG and RnfD in the Rnf complex from Vibrio cholerae.</Title>
-<Xref>DOI:10.1021/bi800920j</Xref>
-<Xref>PMID:18831535</Xref>
-<Note>mass spectrometric detection; EPR spectrographic analysis; mass spectrometric data presented in Figure 4 (but not discussed by the authors) of a phosphopeptide resulting from neutral loss of riboflavin provides proof of the phosphodiester linkage</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>T</SequenceSpec>
-<Xref>GO:0050740</Xref>
-<Xref>PSI-MOD:00354</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>flavoprotein</Keyword>
-<Keyword>FMN</Keyword>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__fmn phosphoryl threonine__t">MOD_RES FMN phosphoryl threonine</Feature>
-</Features>
-<Image src="/images/AA0349.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0349.PDB" />
-</Entry>
-<Entry id="AA0350">
-<Header>
-<Code>AA0350</Code>
-<Dates>
-<CreationDate>31-Oct-2003</CreationDate>
-<StrucRevDate>31-Oct-2003</StrucRevDate>
-<TextChngDate>05-Dec-2008</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-(riboflavin phosphoryl)-L-serine</Name>
-<AlternateName>O3-seryl flavin mononucleotide</AlternateName>
-<AlternateName>O3-seryl FMN</AlternateName>
-<SystematicName>(R)-2-amino-3-(riboflavin 5'-hydrogen phosphonoxy)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 20 H 24 N 5 O 10 P 1</Formula>
-<Weight type="chemical">525.41</Weight>
-<Weight type="physical">525.126079</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 17 H 19 N 4 O 8 P 1</Formula>
-<Weight type="chemical">438.33</Weight>
-<Weight type="physical">438.094050</Weight>
-</CorrectionBlock>
-<Comment>This modification is predicted for proteins homologous to Na(+)-translocating NADH:quinone oxidoreductase B and C chains in certain organisms where the position corresponding to O3-(ribofavin phosphoryl)-threonine instead encodes serine.</Comment>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>GO:0050741</Xref>
-<Xref>PSI-MOD:00355</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>flavoprotein</Keyword>
-<Keyword>FMN</Keyword>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__fmn phosphoryl serine__s">MOD_RES FMN phosphoryl serine</Feature>
-</Features>
-<Image src="/images/AA0350.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0350.PDB" />
-</Entry>
-<Entry id="AA0351">
-<Header>
-<Code>AA0351</Code>
-<Dates>
-<CreationDate>31-Oct-2003</CreationDate>
-<StrucRevDate>31-Oct-2003</StrucRevDate>
-<TextChngDate>30-Apr-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-(4a-FMN)-L-cysteine</Name>
-<AlternateName>4a-(S-cysteinyl)flavin mononucleotide</AlternateName>
-<AlternateName>4a-(S-cysteinyl)FMN</AlternateName>
-<SystematicName>(R)-2-amino-3-(4a-riboflavin 5'-dihydrogen phosphate)sulfanylpropanoic acid</SystematicName>
-<Xref>PDBHET:FMN</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 20 H 26 N 5 O 10 P 1 S 1</Formula>
-<Weight type="chemical">559.49</Weight>
-<Weight type="physical">559.113800</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 17 H 21 N 4 O 9 P 1 S 0</Formula>
-<Weight type="chemical">456.35</Weight>
-<Weight type="physical">456.104615</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Chlumsky, L.J.</Author>
-<Author>Zhang, L.</Author>
-<Author>Ramsey, A.J.</Author>
-<Author>Jorns, M.S.</Author>
-</Authors>
-<Citation>Biochemistry 32, 11132-11142, 1993</Citation>
-<Title>Preparation and properties of recombinant corynebacterial sarcosine oxidase: evidence for posttranslational modification during turnover with sarcosine.</Title>
-<Xref>DOI:10.1021/bi00092a024</Xref>
-<Xref>PMID:7692961</Xref>
-<Note>detection of 4a-FMN cysteinyl adduct as an intermediate</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fedorov, R.</Author>
-<Author>Schlichting, I.</Author>
-<Author>Hartmann, E.</Author>
-<Author>Domratcheva, T.</Author>
-<Author>Fuhrmann, M.</Author>
-<Author>Hegemann, P.</Author>
-</Authors>
-<Citation>Biophys. J. 84, 2474-2482, 2003</Citation>
-<Title>Crystal Structures and Molecular Mechanism of a Light-Induced Signaling Switch: The Phot-LOV1 Domain from Chlamydomonas reinhardtii.</Title>
-<Xref>DOI:10.1021/bi0345135</Xref>
-<Xref>PMID:12668455</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Iwata, T.</Author>
-<Author>Nozaki, D.</Author>
-<Author>Tokutomi, S.</Author>
-<Author>Kagawa, T.</Author>
-<Author>Wada, M.</Author>
-<Author>Kandori, H.</Author>
-</Authors>
-<Citation>Biochemistry 42, 8183-8191, 2003</Citation>
-<Title>Light-induced structural changes in the LOV2 domain of Adiantum phytochrome3 studied by low-temperature FTIR and UV-visible spectroscopy.</Title>
-<Xref>DOI:10.1021/bi0345135</Xref>
-<Xref>PMID:12846567</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Nakasako, M.</Author>
-<Author>Zikihara, K.</Author>
-<Author>Matsuoka, D.</Author>
-<Author>Katsura, H.</Author>
-<Author>Tokutomi, S.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 381, 718-733, 2008</Citation>
-<Title>Structural basis of the LOV1 dimerization of Arabidopsis phototropins 1 and 2.</Title>
-<Xref>DOI:10.1016/j.jmb.2008.06.033</Xref>
-<Xref>PMID:18585389</Xref>
-<Note>X-ray diffraction, 2.00 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Nakasako, M.</Author>
-<Author>Matsuoka, D.</Author>
-<Author>Tokutomi, S.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, July 2007</Citation>
-<Description>Crystal structure of LOV1 domain of phototropin2 from Arabidopsis thaliana.</Description>
-<Xref>PDB:2Z6D</Xref>
-<Note>X-ray diffraction, 2.00 angstroms; the covalent linkage is not annotated in the PDB entries</Note>
-</ReferenceBlock>
-<Comment>This modification forms as an intermediate in light transduction and some redox reactions.</Comment>
-<Comment>The keyword "phosphoprotein" is not used with flavin modifications linked through the flavin.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>GO:0050742</Xref>
-<Xref>PSI-MOD:00356</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>*phosphoprotein</Keyword>
-<Keyword>flavoprotein</Keyword>
-<Keyword>FMN</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__s-4a-fmn cysteine__c">MOD_RES S-4a-FMN cysteine</Feature>
-</Features>
-<Image src="/images/AA0351.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0351.PDB" />
-</Entry>
-<Entry id="AA0352">
-<Header>
-<Code>AA0352</Code>
-<Dates>
-<CreationDate>31-Oct-2003</CreationDate>
-<StrucRevDate>31-Oct-2003</StrucRevDate>
-<TextChngDate>30-Apr-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>1'-(8alpha-FMN)-L-histidine</Name>
-<AlternateName>8alpha-(N(epsilon)-histidyl)FMN</AlternateName>
-<AlternateName>8alpha-(N1'-histidyl)FMN</AlternateName>
-<AlternateName>N(tau)-(8alpha-FMN)-histidine</AlternateName>
-<AlternateName>tele-(8alpha-FMN)-histidine</AlternateName>
-<SystematicName>(S)-2-amino-3-(1-[8alpha riboflavin 5'-dihydrogen phosphate]imidazol-4-yl)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 23 H 26 N 7 O 10 P 1</Formula>
-<Weight type="chemical">591.47</Weight>
-<Weight type="physical">591.147877</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0009">
-<Formula>C 17 H 19 N 4 O 9 P 1</Formula>
-<Weight type="chemical">454.33</Weight>
-<Weight type="physical">454.088965</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Willie, A.</Author>
-<Author>Edmondson, D.E.</Author>
-<Author>Jorns, M.S.</Author>
-</Authors>
-<Citation>Biochemistry 35, 5292-5299, 1996</Citation>
-<Title>Sarcosine oxidase contains a novel covalently bound FMN.</Title>
-<Xref>DOI:10.1021/bi952995h</Xref>
-<Xref>PMID:8611516</Xref>
-<Note>(31)P-NMR, enzymatic and spectrographic characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mukouyama, E.B.</Author>
-<Author>Ohsawa, H.</Author>
-<Author>Suzuki, H.</Author>
-</Authors>
-<Citation>J. Protein Chem. 21, 59-64, 2002</Citation>
-<Title>Cofactors in sarcosine oxidase from Corynebacterium sp. U-96.</Title>
-<Xref>DOI:10.1023/A:1014135216860</Xref>
-<Xref>PMID:11902668</Xref>
-<Note>mass spectrometric, enzymatic and spectrographic characterization</Note>
-</ReferenceBlock>
-<Comment>The arrangement of the attachment has not been completely established in some cases.</Comment>
-<Comment>The keyword "phosphoprotein" is not used with flavin modifications linked through the flavin.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>H</SequenceSpec>
-<Xref>GO:0050743</Xref>
-<Xref>PSI-MOD:00357</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>*phosphoprotein</Keyword>
-<Keyword>flavoprotein</Keyword>
-<Keyword>FMN</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__tele-8alpha-fmn histidine__h">MOD_RES Tele-8alpha-FMN histidine</Feature>
-</Features>
-<Image src="/images/AA0352.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0352.PDB" />
-</Entry>
-<Entry id="AA0353">
-<Header>
-<Code>AA0353</Code>
-<Dates>
-<CreationDate>31-Oct-2003</CreationDate>
-<StrucRevDate>31-Oct-2003</StrucRevDate>
-<TextChngDate>30-Apr-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>3'-(8alpha-FMN)-L-histidine</Name>
-<AlternateName>8alpha-(N(delta)-histidyl)FMN</AlternateName>
-<AlternateName>8alpha-(N3'-histidyl)FMN</AlternateName>
-<AlternateName>N(pi)-(8alpha-FMN)-histidine</AlternateName>
-<AlternateName>pros-(8alpha-FMN)-histidine</AlternateName>
-<SystematicName>(S)-2-amino-3-(3-[8alpha riboflavin 5'-dihydrogen phosphate]imidazol-4-yl)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 23 H 26 N 7 O 10 P 1</Formula>
-<Weight type="chemical">591.47</Weight>
-<Weight type="physical">591.147877</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0009">
-<Formula>C 17 H 19 N 4 O 9 P 1</Formula>
-<Weight type="chemical">454.33</Weight>
-<Weight type="physical">454.088965</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bandeiras, T.M.</Author>
-<Author>Salgueiro, C.</Author>
-<Author>Kletzin, A.</Author>
-<Author>Gomes, C.M.</Author>
-<Author>Teixeira, M.</Author>
-</Authors>
-<Citation>FEBS Lett. 531, 273-277, 2002</Citation>
-<Title>Acidianus ambivalens type-II NADH dehydrogenase: genetic characterisation and identification of the flavin moiety as FMN.</Title>
-<Xref>DOI:10.1016/S0014-5793(02)03514-7</Xref>
-<Xref>PMID:12417325</Xref>
-<Note>(31)P-NMR, enzymatic and spectrographic characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Brito, J.A.</Author>
-<Author>Sousa, F.L.</Author>
-<Author>Stelter, M.</Author>
-<Author>Bandeiras, T.M.</Author>
-<Author>Vonrhein, C.</Author>
-<Author>Teixeira, M.</Author>
-<Author>Pereira, M.M.</Author>
-<Author>Archer, M.</Author>
-</Authors>
-<Citation>Biochemistry 48, 5613-5622, 2009</Citation>
-<Title>Structural and functional insights into sulfide:quinone oxidoreductase.</Title>
-<Xref>DOI:10.1021/bi9003827</Xref>
-<Xref>PMID:19438211</Xref>
-<Note>X-ray diffraction, 2.57 angstroms; reassessment of original report</Note>
-</ReferenceBlock>
-<Comment>In a later publication the authors changed the enzyme activity, the connection from a histidine nitrogen to a cysteine sulfur, and the identity of the flavin from FMN to FAD. They now believe the modification is S-(8alpha-FAD)-L-cysteine, see RESID:AA0143.</Comment>
-<Comment>The keyword "phosphoprotein" is not used with flavin modifications linked through the flavin.</Comment>
-<SequenceCode>
-<SequenceSpec>H</SequenceSpec>
-<Xref>GO:0050744</Xref>
-<Xref>PSI-MOD:00358</Xref>
-</SequenceCode>
-<Source>deprecated</Source>
-<Keywords>
-<Keyword>*phosphoprotein</Keyword>
-<Keyword>flavoprotein</Keyword>
-<Keyword>FMN</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0353.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0353.PDB" />
-</Entry>
-<Entry id="AA0354">
-<Header>
-<Code>AA0354</Code>
-<Dates>
-<CreationDate>28-Nov-2003</CreationDate>
-<StrucRevDate>28-Nov-2003</StrucRevDate>
-<TextChngDate>28-Aug-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N2-acetyl-L-arginine</Name>
-<AlternateName>2-acetamido-5-guanidinopentanoic acid</AlternateName>
-<AlternateName>2-acetylamino-5-guanidinopentanoic acid</AlternateName>
-<AlternateName>acetylarginine</AlternateName>
-<AlternateName>alpha-acetylamino-delta-guanidinovaleric acid</AlternateName>
-<AlternateName>N(alpha)-acetylarginine</AlternateName>
-<SystematicName>(S)-2-acetamido-5-carbamimidamidopentanoic acid</SystematicName>
-<Xref>CAS:155-84-0</Xref>
-<Xref>PDBHET:ACE</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 8 H 15 N 4 O 2</Formula>
-<Weight type="chemical">199.23</Weight>
-<Weight type="physical">199.119501</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0002">
-<Formula>C 2 H 2 N 0 O 1</Formula>
-<Weight type="chemical">42.04</Weight>
-<Weight type="physical">42.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Michel, H.</Author>
-<Author>Griffin, P.R.</Author>
-<Author>Shabanowitz, J.</Author>
-<Author>Hunt, D.F.</Author>
-<Author>Bennett, J.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 266, 17584-17591, 1991</Citation>
-<Title>Tandem mass spectrometry identifies sites of three post-translational modifications of spinach light-harvesting chlorophyll protein II. Proteolytic cleavage, acetylation, and phosphorylation.</Title>
-<Xref>PMID:1894641</Xref>
-<Note>mass spectrometric identification; chemical synthesis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hansson, M.</Author>
-<Author>Vener, A.V.</Author>
-</Authors>
-<Citation>Mol. Cell. Proteomics 2, 550-559, 2003</Citation>
-<Title>Identification of Three Previously Unknown in Vivo Protein Phosphorylation Sites in Thylakoid Membranes of Arabidopsis thaliana.</Title>
-<Xref>DOI:10.1074/mcp.M300050-MCP200</Xref>
-<Xref>PMID:12883043</Xref>
-<Note>mass spectrometric identification</Note>
-</ReferenceBlock>
-<Comment>The common peptide alpha-N-acetyltransferase does not acetylate basic residues, so another alpha-acetyltransferase activity must be producing this modification in a thylakoid protein.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>arginylpeptide alpha-N-acetyltransferase (EC 2.3.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>R</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0048275</Xref>
-<Xref>PSI-MOD:00359</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>acetylated amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n2-acetylarginine__r">MOD_RES N2-acetylarginine</Feature>
-</Features>
-<Image src="/images/AA0354.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0354.PDB" />
-</Entry>
-<Entry id="AA0355">
-<Header>
-<Code>AA0355</Code>
-<Dates>
-<CreationDate>06-Feb-2004</CreationDate>
-<StrucRevDate>06-Feb-2004</StrucRevDate>
-<TextChngDate>31-Dec-2008</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-cysteinyl copper sulfido molybdopterin cytosine dinucleotide</Name>
-<AlternateName>cysteinyl copper mu-sulfido Mo-pterin cytosine dinucleotide</AlternateName>
-<SystematicName>[8-amino-1a,2,4a,5,6,7,10-heptahydro-2-(trihydrogen diphosphate 5'-ester with cytosine)methyl-6-oxo-3,4-dimercapto-pteridino[6,7-5,6]pyranoato-S3,S4]-cysteinyl-S-copper-mu-sulfido-molybdenum hydroxide oxide</SystematicName>
-<Xref>COMe:BIM000360</Xref>
-<Xref>PDBHET:CUN</Xref>
-<Xref>PDBHET:MCN</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 22 Cu 1 H 29 Mo 1 N 9 O 16 P 2 S 4</Formula>
-<Weight type="chemical">1025.20</Weight>
-<Weight type="physical">1025.844039</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 19 Cu 1 H 24 Mo 1 N 8 O 15 P 2 S 3</Formula>
-<Weight type="chemical">922.07</Weight>
-<Weight type="physical">922.834854</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Dobbek, H.</Author>
-<Author>Gremer, L.</Author>
-<Author>Kiefersauer, R.</Author>
-<Author>Huber, R.</Author>
-<Author>Meyer, O.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 99, 15971-15976, 2002</Citation>
-<Title>Catalysis at a dinuclear [CuSMo(==O)OH] cluster in a CO dehydrogenase resolved at 1.1-A resolution.</Title>
-<Xref>DOI:10.1073/pnas.212640899</Xref>
-<Xref>PMID:12475995</Xref>
-<Note>X-ray diffraction, 1.50 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Dobbek, H.</Author>
-<Author>Gremer, L.</Author>
-<Author>Kiefersauer, R.</Author>
-<Author>Huber, R.</Author>
-<Author>Meyer, O.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, November 2002</Citation>
-<Description>Crystal structure of the Cu,Mo-CO dehydrogenase (CODH); oxidized form.</Description>
-<Xref>PDB:1N5W</Xref>
-<Note>X-ray diffraction, 1.50 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Dobbek, H.</Author>
-<Author>Gremer, L.</Author>
-<Author>Kiefersauer, R.</Author>
-<Author>Huber, R.</Author>
-<Author>Meyer, O.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, November 2002</Citation>
-<Description>Crystal structure of the Cu,Mo-CO dehydrogenase (CODH); carbon monoxide reduced state.</Description>
-<Xref>PDB:1N63</Xref>
-<Note>X-ray diffraction, 1.21 angstroms</Note>
-</ReferenceBlock>
-<Comment>A hydrogenated (+4H) structure is shown. The fully oxidized form would be the corresponding 4,9,10-trihydro form.</Comment>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>GO:0050834</Xref>
-<Xref>GO:0050842</Xref>
-<Xref>PSI-MOD:00360</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>copper</Keyword>
-<Keyword>metalloprotein</Keyword>
-<Keyword>molybdenum</Keyword>
-<Keyword>molybdopterin</Keyword>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0355.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0355.PDB" />
-</Entry>
-<Entry id="AA0356">
-<Header>
-<Code>AA0356</Code>
-<Dates>
-<CreationDate>06-Feb-2004</CreationDate>
-<StrucRevDate>06-Feb-2004</StrucRevDate>
-<TextChngDate>25-Feb-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>tris-L-cysteinyl S-adenosylmethion-N,O-diyl tetrairon tetrasulfide</Name>
-<SystematicName>tetra-mu3-sulfido(S-adenosylmethion-N,O-diyliron)tris(S-cysteinyliron)</SystematicName>
-<Xref>COMe:BIM000462</Xref>
-<Xref>PDBHET:SAM</Xref>
-<Xref>PDBHET:SF4</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 24 Fe 4 H 34 N 9 O 8 S 8</Formula>
-<FormalCharge>1-</FormalCharge>
-<Weight type="chemical">1056.45</Weight>
-<Weight type="physical">1055.769901</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005 AA0005">
-<Formula>C 15 Fe 4 H 19 N 6 O 5 S 5</Formula>
-<FormalCharge>1-</FormalCharge>
-<Weight type="chemical">747.03</Weight>
-<Weight type="physical">746.742346</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Berkovitch, F.</Author>
-<Author>Nicolet, Y.</Author>
-<Author>Wan, J.T.</Author>
-<Author>Jarrett, J.T.</Author>
-<Author>Drennan, C.L.</Author>
-</Authors>
-<Citation>Science 303, 76-79, 2004</Citation>
-<Title>Crystal structure of biotin synthase, an S-adenosylmethionine-dependent radical enzyme.</Title>
-<Xref>DOI:10.1126/science.1088493</Xref>
-<Xref>PMID:14704425</Xref>
-<Note>X-ray diffraction, 3.4 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Berkovitch, F.</Author>
-<Author>Nicolet, Y.</Author>
-<Author>Wan, J.T.</Author>
-<Author>Jarrett, J.T.</Author>
-<Author>Drennan, C.L.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, September 2003</Citation>
-<Description>The crystal structure of biotin synthase, an S-adenosylmethionine-dependent radical enzyme.</Description>
-<Xref>PDB:1R30</Xref>
-<Note>X-ray diffraction, 3.4 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sofia, H.J.</Author>
-<Author>Chen, G.</Author>
-<Author>Hetzler, B.G.</Author>
-<Author>Reyes-Spindola, J.F.</Author>
-<Author>Miller, N.E.</Author>
-</Authors>
-<Citation>Nucleic Acids Res. 29, 1097-1106, 2001</Citation>
-<Title>Radical SAM, a novel protein superfamily linking unresolved steps in familiar biosynthetic pathways with radical mechanisms: functional characterization using new analysis and information visualization methods.</Title>
-<Xref>DOI:10.1093/nar/29.5.1097</Xref>
-<Xref>PMID:11222759</Xref>
-<Note>review article</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>C, C, C</SequenceSpec>
-<Condition>cross-link 3</Condition>
-<Xref>GO:0050835</Xref>
-<Xref>PSI-MOD:00361</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>4Fe-4S</Keyword>
-<Keyword>iron-sulfur protein</Keyword>
-<Keyword>metalloprotein</Keyword>
-<Keyword>S-adenosyl-L-methionine</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="metal__iron-sulfur (4fe-4s-s-adomet)__c">METAL Iron-sulfur (4Fe-4S-S-AdoMet)</Feature>
-</Features>
-<Image src="/images/AA0356.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0356.PDB" />
-</Entry>
-<Entry id="AA0357">
-<Header>
-<Code>AA0357</Code>
-<Dates>
-<CreationDate>06-Feb-2004</CreationDate>
-<StrucRevDate>06-Feb-2004</StrucRevDate>
-<TextChngDate>31-Dec-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>tris-L-cysteinyl L-arginyl diiron disulfide</Name>
-<SystematicName>di-mu-sulfido(N(eta1)-arginyl-S-cysteinyliron)(bis-S-cysteinyliron)</SystematicName>
-<Xref>COMe:BIM000469</Xref>
-<Xref>PDBHET:FES</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 15 Fe 2 H 24 N 7 O 4 S 5</Formula>
-<FormalCharge>2-</FormalCharge>
-<Weight type="chemical">638.39</Weight>
-<Weight type="physical">637.920304</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0002 AA0005 AA0005 AA0005">
-<Formula>C 0 Fe 2 H -3 N 0 O 0 S 2</Formula>
-<FormalCharge>2-</FormalCharge>
-<Weight type="chemical">172.79</Weight>
-<Weight type="physical">172.791639</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Berkovitch, F.</Author>
-<Author>Nicolet, Y.</Author>
-<Author>Wan, J.T.</Author>
-<Author>Jarrett, J.T.</Author>
-<Author>Drennan, C.L.</Author>
-</Authors>
-<Citation>Science 303, 76-79, 2004</Citation>
-<Title>Crystal structure of biotin synthase, an S-adenosylmethionine-dependent radical enzyme.</Title>
-<Xref>DOI:10.1126/science.1088493</Xref>
-<Xref>PMID:14704425</Xref>
-<Note>X-ray diffraction, 3.4 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Berkovitch, F.</Author>
-<Author>Nicolet, Y.</Author>
-<Author>Wan, J.T.</Author>
-<Author>Jarrett, J.T.</Author>
-<Author>Drennan, C.L.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, September 2003</Citation>
-<Description>The crystal structure of biotin synthase, an S-adenosylmethionine-dependent radical enzyme.</Description>
-<Xref>PDB:1R30</Xref>
-<Note>X-ray diffraction, 3.4 angstroms</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>C, C, C, R</SequenceSpec>
-<Condition>cross-link 4</Condition>
-<Xref>GO:0050836</Xref>
-<Xref>PSI-MOD:00362</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>2Fe-2S</Keyword>
-<Keyword>iron-sulfur protein</Keyword>
-<Keyword>metalloprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="metal__iron-sulfur (2fe-2s)__r">METAL Iron-sulfur (2Fe-2S)</Feature>
-</Features>
-<Image src="/images/AA0357.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0357.PDB" />
-</Entry>
-<Entry id="AA0358">
-<Header>
-<Code>AA0358</Code>
-<Dates>
-<CreationDate>06-Feb-2004</CreationDate>
-<StrucRevDate>06-Feb-2004</StrucRevDate>
-<TextChngDate>31-Mar-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-cysteinyl-L-selenocysteine</Name>
-<SystematicName>(R,R)-2-amino-3-[3-(2-aminopropanoic acid)sulfanyl]selanylpropanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 8 N 2 O 2 S 1 Se 1</Formula>
-<Weight type="chemical">251.17</Weight>
-<Weight type="physical">251.947170</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005" label="CYS">
-<Formula>C 0 H -2 N 0 O 0 S -1 Se 1</Formula>
-<Weight type="chemical">44.90</Weight>
-<Weight type="physical">45.928800</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0005 AA0022" label="SEC">
-<Formula>C 0 H -2 N 0 O 0 S 0 Se 0</Formula>
-<Weight type="chemical">-2.02</Weight>
-<Weight type="physical">-2.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Zhong, L.</Author>
-<Author>Arner, E.S.</Author>
-<Author>Holmgren, A.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 97, 5854-5859, 2000</Citation>
-<Title>Structure and mechanism of mammalian thioredoxin reductase: the active site is a redox-active selenolthiol/selenenylsulfide formed from the conserved cysteine-selenocysteine sequence.</Title>
-<Xref>DOI:10.1073/pnas.100114897</Xref>
-<Xref>PMID:10801974</Xref>
-<Note>mass spectrometric detection of selenide-sulfide bond</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ma, S.</Author>
-<Author>Hill, K.E.</Author>
-<Author>Burk, R.F.</Author>
-<Author>Caprioli, R.M.</Author>
-</Authors>
-<Citation>Biochemistry 42, 9703-9711, 2003</Citation>
-<Title>Mass spectrometric identification of N- and O-glycosylation sites of full-length rat selenoprotein P and determination of selenide-sulfide and disulfide linkages in the shortest isoform.</Title>
-<Xref>DOI:10.1021/bi0346300</Xref>
-<Xref>PMID:12911312</Xref>
-<Note>mass spectrometric detection of selenide-sulfide bond</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Metanis, N.</Author>
-<Author>Keinan, E.</Author>
-<Author>Dawson, P.E.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 128, 16684-16691, 2006</Citation>
-<Title>Synthetic seleno-glutaredoxin 3 analogues are highly reducing oxidoreductases with enhanced catalytic efficiency.</Title>
-<Xref>DOI:10.1021/ja0661414</Xref>
-<Xref>PMID:17177418</Xref>
-<Note>comparative redox potentials of cystine, cysteinylselenocysteine and selenocystine in synthetic glutaredoxins with a [C/U]XX[C/U] motif</Note>
-</ReferenceBlock>
-<Comment>The experimental redox potential of cysteinylselenocysteine in synthetic glutaredoxin 3 is -260 to -275 mV. See RESID:AA0025 and RESID:AA0437.</Comment>
-<SequenceCode link="CYS">
-<SequenceSpec>C, C</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Condition>secondary to RESID:AA0022</Condition>
-<Xref>GO:0050837</Xref>
-<Xref>PSI-MOD:00867</Xref>
-</SequenceCode>
-<SequenceCode link="SEC">
-<SequenceSpec>C, U</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:00363</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>redox-active center</Keyword>
-<Keyword>selenium</Keyword>
-<Keyword>selenocysteine</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__cysteinyl-selenocysteine (cys-sec)__c__u">CROSSLNK Cysteinyl-selenocysteine (Cys-Sec)</Feature>
-<Feature type="UniProt" key="crosslnk__cysteinyl-selenocysteine (sec-cys)__u__c">CROSSLNK Cysteinyl-selenocysteine (Sec-Cys)</Feature>
-</Features>
-<Image src="/images/AA0358.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0358.PDB" />
-</Entry>
-<Entry id="AA0359">
-<Header>
-<Code>AA0359</Code>
-<Dates>
-<CreationDate>06-Feb-2004</CreationDate>
-<StrucRevDate>06-Feb-2004</StrucRevDate>
-<TextChngDate>31-May-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>5-hydroxy-N6,N6,N6-trimethyl-L-lysine</Name>
-<AlternateName>(2Xi,5S)-5-amino-5-carboxy-2-hydroxy-N,N,N-trimethylpentanaminium</AlternateName>
-<AlternateName>(2Xi,5S)-5-azanyl-5-carboxy-2-hydroxy-N,N,N-trimethylpentanazanium</AlternateName>
-<AlternateName>5-hydroxy-N(zeta)-trimethyllysine</AlternateName>
-<AlternateName>5-hydroxy-N6,N6,N6-trimethyllysin-N6-ium</AlternateName>
-<AlternateName>5-hydroxy-N6,N6,N6-trimethyllysine cation</AlternateName>
-<AlternateName>alpha-amino-epsilon-dimethylamino-delta-hydroxycaproic acid</AlternateName>
-<AlternateName>delta-hydroxy-epsilon-N,N,N-trimethyllysine</AlternateName>
-<AlternateName>lysine derivative Lys(z)</AlternateName>
-<SystematicName>(2R,5Xi)-5-amino-5-carboxy-2-hydroxy-N,N,N-trimethylpentan-1-aminium</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 19 N 2 O 2</Formula>
-<FormalCharge>1+</FormalCharge>
-<Weight type="chemical">187.26</Weight>
-<Weight type="physical">187.144104</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 3 H 7 N 0 O 1</Formula>
-<FormalCharge>1+</FormalCharge>
-<Weight type="chemical">59.09</Weight>
-<Weight type="physical">59.049141</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kroeger, N.</Author>
-<Author>Deutzmann, R.</Author>
-<Author>Sumper, M.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 276, 26066-26070, 2001</Citation>
-<Title>Silica-precipitating peptides from diatoms. The chemical structure of silaffin-A from Cylindrotheca fusiformis.</Title>
-<Xref>DOI:10.1074/jbc.M102093200</Xref>
-<Xref>PMID:11349130</Xref>
-<Note>chromatographic and mass spectrometric identification</Note>
-</ReferenceBlock>
-<Comment>Hydroxylation at C-5 is assumed. Neither the position of the hydroxylation nor the stereochemistry for the second chiral center it produces have been determined. The (2S,5R) diastereomer is shown.</Comment>
-<Comment>Consult FAQ at http://pir.georgetown.edu/resid/faq.shtml#q12 concerning calculation of the difference formula.</Comment>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Condition>incidental to RESID:AA0278</Condition>
-<Condition>secondary to RESID:AA0028</Condition>
-<Condition>secondary to RESID:AA0074</Condition>
-<Xref>GO:0050838</Xref>
-<Xref>GO:0050841</Xref>
-<Xref>PSI-MOD:00364</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-<Keyword>methylated amino acid</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n6,n6,n6-trimethyl-5-hydroxylysine__k">MOD_RES N6,N6,N6-trimethyl-5-hydroxylysine</Feature>
-</Features>
-<Image src="/images/AA0359.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0359.PDB" />
-</Entry>
-<Entry id="AA0360">
-<Header>
-<Code>AA0360</Code>
-<Dates>
-<CreationDate>27-Feb-2004</CreationDate>
-<StrucRevDate>27-Feb-2004</StrucRevDate>
-<TextChngDate>29-Oct-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-(L-isoglutamyl)-glycine</Name>
-<AlternateName>2-amino-N5-(carboxymethyl)-pentanediamic acid</AlternateName>
-<AlternateName>isoglutamyl glycine</AlternateName>
-<AlternateName>N-gamma-glutamylglycine</AlternateName>
-<SystematicName>(S)-2-amino-5-(carboxymethyl)amino-5-oxopentanoic acid</SystematicName>
-<Xref>CAS:1948-29-4</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 9 N 2 O 3</Formula>
-<Weight type="chemical">169.16</Weight>
-<Weight type="physical">169.061317</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0006 AA0008">
-<Formula>C 0 H -2 N 0 O -1</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bayro, M.J.</Author>
-<Author>Mukhopadhyay, J.</Author>
-<Author>Swapna, G.V.T.</Author>
-<Author>Huang, J.Y.</Author>
-<Author>Ma, L.-C.</Author>
-<Author>Sineva, E.</Author>
-<Author>Dawson, P.E.</Author>
-<Author>Montelione, G.T.</Author>
-<Author>Ebright, R.H.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 125, 12382-12383, 2003</Citation>
-<Title>Structure of antibacterial peptide microcin J25: a 21-residue lariat protoknot.</Title>
-<Xref>DOI:10.1021/ja036677e</Xref>
-<Xref>PMID:14531661</Xref>
-<Note>the initials of G.V.T. Swapna in the PubMed citation are corrected</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bayro, M.J.</Author>
-<Author>Swapna, G.V.T.</Author>
-<Author>Huang, J.Y.</Author>
-<Author>Ma, L.-C.</Author>
-<Author>Mukhopadhyay, J.</Author>
-<Author>Ebright, R.H.</Author>
-<Author>Montelione, G.T.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, June 2003</Citation>
-<Description>Structure of antibacterial peptide microcin J25: a 21-residue lariat protoknot.</Description>
-<Xref>PDB:1PP5</Xref>
-<Note>solution structure by (1)H-, (13)C- and (15)N-NMR</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wilson, K.A.</Author>
-<Author>Kalkum, M.</Author>
-<Author>Ottesen, J.</Author>
-<Author>Yuzenkova, J.</Author>
-<Author>Chait, B.T.</Author>
-<Author>Landick, R.</Author>
-<Author>Muir, T.</Author>
-<Author>Severinov, K.</Author>
-<Author>Darst, S.A.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 125, 12475-12483, 2003</Citation>
-<Title>Structure of microcin J25, a peptide inhibitor of bacterial RNA polymerase, is a lassoed tail.</Title>
-<Xref>DOI:10.1021/ja036756q</Xref>
-<Xref>PMID:14531691</Xref>
-<Note>mass spectrometric and (1)H-NMR identification; chemical synthesis</Note>
-</ReferenceBlock>
-<Comment>For the "lariat" or "lasso" cross-link between glycine and aspartic acid, see RESID:AA0126.</Comment>
-<SequenceCode>
-<SequenceSpec>E, G</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Condition>cross-link 2</Condition>
-<Xref>GO:0050986</Xref>
-<Xref>PSI-MOD:00365</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-<Keyword>isopeptide bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__isoglutamyl glycine isopeptide (gly-glu)__g__e">CROSSLNK Isoglutamyl glycine isopeptide (Gly-Glu)</Feature>
-</Features>
-<Image src="/images/AA0360.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0360.PDB" />
-</Entry>
-<Entry id="AA0361">
-<Header>
-<Code>AA0361</Code>
-<Dates>
-<CreationDate>27-Feb-2004</CreationDate>
-<StrucRevDate>27-Feb-2004</StrucRevDate>
-<TextChngDate>31-Dec-2008</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-sulfo-L-serine</Name>
-<AlternateName>2-amino-3-hydroxypropanoic acid 3-sulfate</AlternateName>
-<AlternateName>O3-sulfonoserine</AlternateName>
-<AlternateName>O3-sulfoserine</AlternateName>
-<AlternateName>serine sulfate ester</AlternateName>
-<SystematicName>(2S)-2-amino-3-(sulfooxy)propanoic acid</SystematicName>
-<Xref>CAS:626-69-7</Xref>
-<Xref>PDBHET:OSE</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 5 N 1 O 5 S 1</Formula>
-<Weight type="chemical">167.13</Weight>
-<Weight type="physical">166.988843</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 0 H 0 N 0 O 3 S 1</Formula>
-<Weight type="chemical">80.06</Weight>
-<Weight type="physical">79.956815</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Medzihradszky, K.F.</Author>
-<Author>Darula, Z.</Author>
-<Author>Perlson, E.</Author>
-<Author>Fainzilber, M.</Author>
-<Author>Chalkley, R.J.</Author>
-<Author>Ball, H.</Author>
-<Author>Greenbaum, D.</Author>
-<Author>Bogyo, M.</Author>
-<Author>Tyson, D.R.</Author>
-<Author>Bradshaw, R.A.</Author>
-<Author>Burlingame, A.L.</Author>
-</Authors>
-<Citation>Mol. Cell. Proteomics 3, 429-440, 2004</Citation>
-<Title>O-Sulfonation of serine and threonine - mass spectrometric detection and characterization of a new posttranslational modification in diverse proteins throughout the eukaryotes.</Title>
-<Xref>DOI:10.1074/mcp.M300140-MCP200</Xref>
-<Xref>PMID:14752058</Xref>
-<Note>chromatographic detection; mass spectrometric identification</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>GO:0050984</Xref>
-<Xref>GO:0050987</Xref>
-<Xref>PSI-MOD:00366</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>sulfoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__sulfoserine__s">MOD_RES Sulfoserine</Feature>
-</Features>
-<Image src="/images/AA0361.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0361.PDB" />
-</Entry>
-<Entry id="AA0362">
-<Header>
-<Code>AA0362</Code>
-<Dates>
-<CreationDate>27-Feb-2004</CreationDate>
-<StrucRevDate>27-Feb-2004</StrucRevDate>
-<TextChngDate>31-Dec-2008</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-sulfo-L-threonine</Name>
-<AlternateName>2-amino-3-hydroxybutanoic acid 3-sulfate</AlternateName>
-<AlternateName>O3-sulfonothreonine</AlternateName>
-<AlternateName>O3-sulfothreonine</AlternateName>
-<AlternateName>threonine sulfate ester</AlternateName>
-<SystematicName>(2S,3R)-2-amino-3-(sulfooxy)butanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 7 N 1 O 5 S 1</Formula>
-<Weight type="chemical">181.16</Weight>
-<Weight type="physical">181.004493</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0017">
-<Formula>C 0 H 0 N 0 O 3 S 1</Formula>
-<Weight type="chemical">80.06</Weight>
-<Weight type="physical">79.956815</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Medzihradszky, K.F.</Author>
-<Author>Darula, Z.</Author>
-<Author>Perlson, E.</Author>
-<Author>Fainzilber, M.</Author>
-<Author>Chalkley, R.J.</Author>
-<Author>Ball, H.</Author>
-<Author>Greenbaum, D.</Author>
-<Author>Bogyo, M.</Author>
-<Author>Tyson, D.R.</Author>
-<Author>Bradshaw, R.A.</Author>
-<Author>Burlingame, A.L.</Author>
-</Authors>
-<Citation>Mol. Cell. Proteomics 3, 429-440, 2004</Citation>
-<Title>O-Sulfonation of serine and threonine - mass spectrometric detection and characterization of a new posttranslational modification in diverse proteins throughout the eukaryotes.</Title>
-<Xref>DOI:10.1074/mcp.M300140-MCP200</Xref>
-<Xref>PMID:14752058</Xref>
-<Note>chromatographic detection; mass spectrometric identification</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>T</SequenceSpec>
-<Xref>GO:0050985</Xref>
-<Xref>GO:0050991</Xref>
-<Xref>PSI-MOD:00367</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>sulfoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__sulfothreonine__t">MOD_RES Sulfothreonine</Feature>
-</Features>
-<Image src="/images/AA0362.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0362.PDB" />
-</Entry>
-<Entry id="AA0363">
-<Header>
-<Code>AA0363</Code>
-<Dates>
-<CreationDate>27-Feb-2004</CreationDate>
-<StrucRevDate>27-Feb-2004</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-carboxy-L-methionine</Name>
-<AlternateName>2-carbamic-4-(methylsulfanyl)butanoic acid</AlternateName>
-<AlternateName>2-carbamic-4-(methylthio)butanoic acid</AlternateName>
-<AlternateName>N-carboxymethionine</AlternateName>
-<SystematicName>(S)-2-carboxyamino-4-(methylsulfanyl)butanoic acid</SystematicName>
-<Xref>ChEBI:61924</Xref>
-<Xref>PDBHET:CXM</Xref>
-<Xref>PDBHET:FMT</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 10 N 1 O 3 S 1</Formula>
-<Weight type="chemical">176.21</Weight>
-<Weight type="physical">176.038139</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0013">
-<Formula>C 1 H 0 N 0 O 2 S 0</Formula>
-<Weight type="chemical">44.01</Weight>
-<Weight type="physical">43.989829</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fauman, E.B.</Author>
-<Author>Rutenber, E.E.</Author>
-<Author>Maley, G.F.</Author>
-<Author>Maley, F.</Author>
-<Author>Stroud, R.M.</Author>
-</Authors>
-<Citation>Biochemistry 33, 1502-1511, 1994</Citation>
-<Title>Water-mediated substrate/product discrimination: the product complex of thymidylate synthase at 1.83 A.</Title>
-<Xref>DOI:10.1021/bi00172a029</Xref>
-<Xref>PMID:8312270</Xref>
-<Note>X-ray diffraction, 1.83 angstroms; the modification is described as "a carbamate involving the N-terminal nitrogen"</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fauman, E.</Author>
-<Author>Rutenber, E.</Author>
-<Author>Stroud, R.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, May 1993</Citation>
-<Description>Thymidylate synthase (E.C.2.1.1.45) mutant with Cys 146 replaced by Ser (C146S).</Description>
-<Xref>PDB:1TYS</Xref>
-<Note>X-ray diffraction, 1.83 angstroms; the modification is described as "a formate group bound to N of Met 1 forming a carbamate group"</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Benini, S.</Author>
-<Author>Rypniewski, W.R.</Author>
-<Author>Wilson, K.S.</Author>
-<Author>Miletti, S.</Author>
-<Author>Ciurli, S.</Author>
-<Author>Mangani, S.</Author>
-</Authors>
-<Citation>Structure 7, 205-216, 1999</Citation>
-<Title>A new proposal for urease mechanism based on the crystal structures of the native and inhibited enzyme from Bacillus pasteurii: why urea hydrolysis costs two nickels.</Title>
-<Xref>DOI:10.1016/S0969-2126(99)80026-4</Xref>
-<Xref>PMID:10368287</Xref>
-<Note>X-ray diffraction, 2.0 angstroms; the modification is described as "a formate group bound to N of Met 1 forming a carbamate group"</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Benini, S.</Author>
-<Author>Rypniewski, W.R.</Author>
-<Author>Wilson, K.S.</Author>
-<Author>Ciurli, S.</Author>
-<Author>Mangani, S.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, April 2001</Citation>
-<Description>Phosphate inhibited Bacillus pasteurii urease crystal structure.</Description>
-<Xref>PDB:1IE7</Xref>
-<Note>X-ray diffraction, 1.85 angstroms; modeled earlier as an acetyl group in PDB:2UBP</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Papiz, M.Z.</Author>
-<Author>Prince, S.M.</Author>
-<Author>Howard, T.</Author>
-<Author>Cogdell, R.J.</Author>
-<Author>Isaacs, N.W.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 326, 1523-1538, 2003</Citation>
-<Title>The structure and thermal motion of the B800-850 LH2 complex from Rps. acidophila at 2.0 angstroms resolution and 100 K: new structural features and functionally relevant motions.</Title>
-<Xref>DOI:10.1016/S0022-2836(03)00024-X</Xref>
-<Xref>PMID:12595263</Xref>
-<Note>X-ray diffraction, 2.0 angstroms; the formyl group ligand is remodeled with two oxygens as a carboxyl group, but appears to be tetrahedral rather than trigonal planar</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Papiz, M.Z.</Author>
-<Author>Prince, S.M.</Author>
-<Author>Howard, T.</Author>
-<Author>Cogdell, R.J.</Author>
-<Author>Isaacs, N.W.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, September 1994</Citation>
-<Description>Crystal structure LH2 B800-850 from Rps. acidophila at 2.0 angstrom resolution.</Description>
-<Xref>PDB:1NKZ</Xref>
-<Note>X-ray diffraction, 2.0 angstroms; the formyl group ligand is remodeled with two oxygens as a carboxyl group, but appears to be tetrahedral rather than trigonal planar</Note>
-</ReferenceBlock>
-<Comment>At least three protein crystallographic structures have been reported with this modification. However, no chemical evidence for this modification is provided, there were no reports of this modification before these crystallographic reports, and there is no metabolic explanation for the conversion of a formyl group to a carboxy group. There is confusion in its description, and misnaming is common.</Comment>
-<Comment>This modification is probably a misidentification of N-(dihydroxymethyl)methionine, the hydrated form of N-formylmethionine. See RESID:AA0493.</Comment>
-<SequenceCode>
-<SequenceSpec>M</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0050988</Xref>
-<Xref>PSI-MOD:00368</Xref>
-</SequenceCode>
-<Source>deprecated</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this dubious modification is not currently annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0363.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0363.PDB" />
-</Entry>
-<Entry id="AA0364">
-<Header>
-<Code>AA0364</Code>
-<Dates>
-<CreationDate>31-Mar-2004</CreationDate>
-<StrucRevDate>31-Mar-2004</StrucRevDate>
-<TextChngDate>31-Mar-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-acetyl-L-serine</Name>
-<AlternateName>O-acetylserine</AlternateName>
-<AlternateName>serine acetate ester</AlternateName>
-<SystematicName>(2S)-3-(acetyloxy)-2-aminopropanoic acid</SystematicName>
-<Xref>CAS:4985-36-8</Xref>
-<Xref>ChEBI:17981</Xref>
-<Xref>PDBHET:OAS</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 7 N 1 O 3</Formula>
-<Weight type="chemical">129.12</Weight>
-<Weight type="physical">129.042593</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 2 H 2 N 0 O 1</Formula>
-<Weight type="chemical">42.04</Weight>
-<Weight type="physical">42.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Rudman, D.</Author>
-<Author>Chawla, R.K.</Author>
-<Author>Hollins, B.M.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 254, 10102-10108, 1979</Citation>
-<Title>N,O-Diacetylserine-1 alpha-melanocyte-stimulating hormone, a naturally occurring melanotropic peptide.</Title>
-<Xref>PMID:489587</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Buckley, D.I.</Author>
-<Author>Houghten, R.A.</Author>
-<Author>Ramachandran, J.</Author>
-</Authors>
-<Citation>Int. J. Pept. Protein Res. 17, 508-513, 1981</Citation>
-<Title>Isolation of alpha-melanotropin and N, O-diacetylserine1-alpha-melanotropin from porcine pituitary extracts.</Title>
-<Xref>PMID:7309355</Xref>
-<Note>in this report it is not clear whether O-acetylation is separately catalyzed from N-acetylation, or follows from it by internal transacetylation</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mukherjee, S.</Author>
-<Author>Keitany, G.</Author>
-<Author>Li, Y.</Author>
-<Author>Wang, Y.</Author>
-<Author>Ball, H.L.</Author>
-<Author>Goldsmith, E.J.</Author>
-<Author>Orth, K.</Author>
-</Authors>
-<Citation>Science 312, 1211-1214, 2006</Citation>
-<Title>Yersinia YopJ acetylates and inhibits kinase activation by blocking phosphorylation.</Title>
-<Xref>DOI:10.1126/science.1126867</Xref>
-<Xref>PMID:16728640</Xref>
-<Note>O-acetylation of serine in host kinases is catalyzed by yersinia toxin blocking the normal phosphorylation</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Condition>incidental to RESID:AA0051</Condition>
-<Xref>GO:0030919</Xref>
-<Xref>PSI-MOD:00369</Xref>
-<Xref>PSI-MOD:00648</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="mod_res__o-acetylserine__s">MOD_RES O-acetylserine</Feature>
-</Features>
-<Image src="/images/AA0364.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0364.PDB" />
-</Entry>
-<Entry id="AA0365">
-<Header>
-<Code>AA0365</Code>
-<Dates>
-<CreationDate>31-Mar-2004</CreationDate>
-<StrucRevDate>31-Mar-2004</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>(E)-2,3-didehydrotyrosine</Name>
-<AlternateName>amino-(para-hydroxybenzylidenyl)acetic acid</AlternateName>
-<AlternateName>blue non-fluorescent pocilloporin chromophore</AlternateName>
-<AlternateName>para-hydroxybenzylidene-imidazolidinone chromophore</AlternateName>
-<AlternateName>trans-dehydrotyrosine</AlternateName>
-<SystematicName>(2E)-2-amino-3-(4-hydroxyphenyl)prop-2-enoic acid</SystematicName>
-<Xref>PDBHET:CRK</Xref>
-<Xref>PDBHET:CRQ</Xref>
-<Xref>PDBHET:NRQ</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 7 N 1 O 2</Formula>
-<Weight type="chemical">161.16</Weight>
-<Weight type="physical">161.047678</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0019">
-<Formula>C 0 H -2 N 0 O 0</Formula>
-<Weight type="chemical">-2.02</Weight>
-<Weight type="physical">-2.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Prescott, M.</Author>
-<Author>Ling, M.</Author>
-<Author>Beddoe, T.</Author>
-<Author>Oakley, A.J.</Author>
-<Author>Dove, S.</Author>
-<Author>Hoegh-Guldberg, O.</Author>
-<Author>Devenish, R.J.</Author>
-<Author>Rossjohn, J.</Author>
-</Authors>
-<Citation>Structure 11, 275-284, 2003</Citation>
-<Title>The 2.2 A crystal structure of a pocilloporin pigment reveals a nonplanar chromophore conformation.</Title>
-<Xref>DOI:10.1016/S0969-2126(03)00028-5</Xref>
-<Xref>PMID:12623015</Xref>
-<Note>X-ray diffraction, 2.2 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Prescott, M.</Author>
-<Author>Ling, M.</Author>
-<Author>Beddoe, T.</Author>
-<Author>Oakley, A.J.</Author>
-<Author>Dove, S.</Author>
-<Author>Hoegh-Guldberg, O.</Author>
-<Author>Devenish, R.J.</Author>
-<Author>Rossjohn, J.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, September 2002</Citation>
-<Description>Crystal structure of coral pigment.</Description>
-<Xref>PDB:1MOU</Xref>
-<Note>X-ray diffraction, 2.2 angstroms</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>Y</SequenceSpec>
-<Condition>incidental to RESID:AA0184</Condition>
-<Condition>incidental to RESID:AA0187</Condition>
-<Condition>incidental to RESID:AA0188</Condition>
-<Condition>incidental to RESID:AA0189</Condition>
-<Condition>incidental to RESID:AA0378</Condition>
-<Condition>incidental to RESID:AA0379</Condition>
-<Condition>incidental to RESID:AA0380</Condition>
-<Condition>incidental to RESID:AA0381</Condition>
-<Xref>GO:0018251</Xref>
-<Xref>GO:0030922</Xref>
-<Xref>PSI-MOD:00370</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="mod_res__(e)-2,3-didehydrotyrosine__y">MOD_RES (E)-2,3-didehydrotyrosine</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="mod_res__2,3-didehydrotyrosine__y">MOD_RES 2,3-didehydrotyrosine</Feature>
-<Note>this UniProt feature is used when the isomeric structure has not been determined</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0365.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0365.PDB" />
-</Entry>
-<Entry id="AA0366">
-<Header>
-<Code>AA0366</Code>
-<Dates>
-<CreationDate>31-Mar-2004</CreationDate>
-<StrucRevDate>31-Mar-2004</StrucRevDate>
-<TextChngDate>01-Mar-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>bis-L-aspartato tris-L-glutamato L-histidino calcium tetramanganese tetroxide</Name>
-<AlternateName>4Mn-Ca-4O cluster</AlternateName>
-<AlternateName>photosystem II catalytic cluster</AlternateName>
-<SystematicName>mu3-1:2:3kappaO-oxido-mu3-1:3:4kappaO-oxido-mu3-2:3:4kappaO-oxido-mu4-1:2:4:5kappaO-oxido-N1'-histidino-O5-glutamato 2-manganese-O5,O5-glutamato 3-manganese-O4-aspartato 4-manganese-O4-aspartato-O5-glutamato 5-manganese</SystematicName>
-<Xref>PDBHET:OEC</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 29 Ca 1 H 32 Mn 4 N 8 O 20</Formula>
-<Weight type="chemical">1072.44</Weight>
-<Weight type="physical">1071.888057</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0004 AA0004 AA0006 AA0006 AA0006 AA0009">
-<Formula>C 0 Ca 1 H -6 Mn 4 N 0 O 4</Formula>
-<Weight type="chemical">317.78</Weight>
-<Weight type="physical">317.647480</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ferreira, K.N.</Author>
-<Author>Iverson, T.M.</Author>
-<Author>Maghlaoui, K.</Author>
-<Author>Barber, J.</Author>
-<Author>Iwata, S.</Author>
-</Authors>
-<Citation>Science 303, 1831-1838, 2004</Citation>
-<Title>Architecture of the photosynthetic oxygen-evolving center.</Title>
-<Xref>DOI:10.1126/science.1093087</Xref>
-<Xref>PMID:14764885</Xref>
-<Note>X-ray diffraction, 3.5 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ferreira, K.N.</Author>
-<Author>Iverson, T.M.</Author>
-<Author>Maghlaoui, K.</Author>
-<Author>Barber, J.</Author>
-<Author>Iwata, S.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, January 2004</Citation>
-<Description>Architecture of the photosynthetic oxygen evolving center.</Description>
-<Xref>PDB:1S5L</Xref>
-<Note>X-ray diffraction, 3.5 angstroms</Note>
-</ReferenceBlock>
-<Comment>The metal cluster was modeled as a three manganese, calcium, four oxygen cubane with one oxygen ligating the calcium also ligating a fourth manganese. The reactive center for converting several water molecules to dioxygen may be between the calcium and the fourth manganese where electron density was modeled as bicarbonate and chloride ions.</Comment>
-<Comment>Because of the uncertainty in the structure, a formal charge cannot be calculated.</Comment>
-<Comment>This model for the photosystem II catalytic cluster has been superseded by RESID:AA0600.</Comment>
-<SequenceCode>
-<SequenceSpec>D, D, E, E, E, H</SequenceSpec>
-<Condition>cross-link 6</Condition>
-<Xref>GO:0030926</Xref>
-<Xref>GO:0030927</Xref>
-<Xref>PSI-MOD:00371</Xref>
-</SequenceCode>
-<Source>deprecated</Source>
-<Keywords>
-<Keyword>calcium</Keyword>
-<Keyword>manganese</Keyword>
-<Keyword>metalloprotein</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0366.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0366.PDB" />
-</Entry>
-<Entry id="AA0367">
-<Header>
-<Code>AA0367</Code>
-<Dates>
-<CreationDate>30-Jun-2004</CreationDate>
-<StrucRevDate>30-Jun-2004</StrucRevDate>
-<TextChngDate>30-Jun-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>3'-(L-tyros-3'-yl)-L-tyrosine</Name>
-<AlternateName>6,6'-dihydroxy-(1,1'-biphenyl)-3,3'-bis(2-aminopropanoic acid)</AlternateName>
-<AlternateName>alpha,alpha'-diamino-6,6'-dihydroxy-(1,1'-biphenyl)-3,3'-dipropanoic acid</AlternateName>
-<AlternateName>bityrosine</AlternateName>
-<AlternateName>o,o-dityrosine</AlternateName>
-<SystematicName>(2S,2'S)-3,3'-(6,6'-dihydroxybiphenyl-3,3'-diyl)bis(2-aminopropanoic acid)</SystematicName>
-<Xref>CAS:980-21-2</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 18 H 16 N 2 O 4</Formula>
-<Weight type="chemical">324.34</Weight>
-<Weight type="physical">324.111007</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0019 AA0019">
-<Formula>C 0 H -2 N 0 O 0</Formula>
-<Weight type="chemical">-2.02</Weight>
-<Weight type="physical">-2.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Andersen, S.O.</Author>
-</Authors>
-<Citation>Biochim. Biophys. Acta 93, 213-215, 1964</Citation>
-<Title>The cross-links in resilin identified as dityrosine and trityrosine.</Title>
-<Xref>DOI:10.1016/0304-4165(64)90289-2</Xref>
-<Xref>PMID:14249161</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>DeVore, D.P.</Author>
-<Author>Gruebel, R.J.</Author>
-</Authors>
-<Citation>Biochem. Biophys. Res. Commun. 80, 993-999, 1978</Citation>
-<Title>Dityrosine in adhesive formed by the sea mussel, Mytilus edulis.</Title>
-<Xref>DOI:10.1016/0006-291X(78)91343-8</Xref>
-<Xref>PMID:637884</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Malencik, D.A.</Author>
-<Author>Sprouse, J.F.</Author>
-<Author>Swanson, C.A.</Author>
-<Author>Anderson, S.R.</Author>
-</Authors>
-<Citation>Anal. Biochem. 242, 202-213, 1996</Citation>
-<Title>Dityrosine: preparation, isolation, and analysis.</Title>
-<Xref>DOI:10.1006/abio.1996.0454</Xref>
-<Xref>PMID:8937563</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Jacob, J.S.</Author>
-<Author>Cistola, D.P.</Author>
-<Author>Hsu, F.F.</Author>
-<Author>Muzaffar, S.</Author>
-<Author>Mueller, D.M.</Author>
-<Author>Hazen, S.L.</Author>
-<Author>Heinecke, J.W.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 271, 19950-19956, 1996</Citation>
-<Title>Human phagocytes employ the myeloperoxidase-hydrogen peroxide system to synthesize dityrosine, trityrosine, pulcherosine, and isodityrosine by a tyrosyl radical-dependent pathway.</Title>
-<Xref>DOI:10.1074/jbc.271.33.19950</Xref>
-<Xref>PMID:8702710</Xref>
-<Note>biosynthesis</Note>
-</ReferenceBlock>
-<Comment>This cross-link can be produced as an oxidation artifact, or enzymatically by enzymes like myeloperoxidase. Since the enzymatic reaction proceeds by a free-radical mechanism, the cross-link can be aleatoric with 2, 3 or 4 tyrosines rings becoming linked in several possible ways.  See also RESID:AA0368.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>myeloperoxidase (EC 1.11.1.7)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>Y, Y</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>GO:0030959</Xref>
-<Xref>PSI-MOD:00372</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>aleatoric crosslink</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0367.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0367.PDB" />
-</Entry>
-<Entry id="AA0368">
-<Header>
-<Code>AA0368</Code>
-<Dates>
-<CreationDate>30-Jun-2004</CreationDate>
-<StrucRevDate>30-Jun-2004</StrucRevDate>
-<TextChngDate>30-Jun-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>3'-(L-tyros-O4'-yl)-L-tyrosine</Name>
-<AlternateName>2-amino-3-[4-(5-[(2S)-2-amino-2-carboxyethyl]-2-hydroxyphenoxy)phenyl]propanoic acid</AlternateName>
-<AlternateName>isodityrosine</AlternateName>
-<AlternateName>O-(5-(2-amino-2-carboxyethyl)-2-hydroxyphenyl)-L-tyrosine</AlternateName>
-<SystematicName>(2S)-2-amino-3-[3-(4-[(2S)-2-amino-2-carboxyethyl]phenoxy)-4-hydroxyphenyl]propanoic acid</SystematicName>
-<Xref>CAS:83118-65-4</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 18 H 16 N 2 O 4</Formula>
-<Weight type="chemical">324.34</Weight>
-<Weight type="physical">324.111007</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0019 AA0019">
-<Formula>C 0 H -2 N 0 O 0</Formula>
-<Weight type="chemical">-2.02</Weight>
-<Weight type="physical">-2.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fry, S.C.</Author>
-</Authors>
-<Citation>Biochem. J. 204, 449-455, 1982</Citation>
-<Title>Isodityrosine, a new cross-linking amino acid from plant cell-wall glycoprotein.</Title>
-<Xref>PMID:7115340</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Jacob, J.S.</Author>
-<Author>Cistola, D.P.</Author>
-<Author>Hsu, F.F.</Author>
-<Author>Muzaffar, S.</Author>
-<Author>Mueller, D.M.</Author>
-<Author>Hazen, S.L.</Author>
-<Author>Heinecke, J.W.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 271, 19950-19956, 1996</Citation>
-<Title>Human phagocytes employ the myeloperoxidase-hydrogen peroxide system to synthesize dityrosine, trityrosine, pulcherosine, and isodityrosine by a tyrosyl radical-dependent pathway.</Title>
-<Xref>DOI:10.1074/jbc.271.33.19950</Xref>
-<Xref>PMID:8702710</Xref>
-<Note>biosynthesis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Milani, M.</Author>
-<Author>Savard, P.Y.</Author>
-<Author>Ouellet, H.</Author>
-<Author>Ascenzi, P.</Author>
-<Author>Guertin, M.</Author>
-<Author>Bolognesi, M.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 100, 5766-5771, 2003</Citation>
-<Title>A TyrCD1/TrpG8 hydrogen bond network and a TyrB10--TyrCD1 covalent link shape the heme distal site of Mycobacterium tuberculosis hemoglobin O.</Title>
-<Xref>DOI:10.1073/pnas.1037676100</Xref>
-<Xref>PMID:12719529</Xref>
-<Note>X-ray diffraction, 2.1 angstroms; mass spectrometric detection; this is an apparently specific formation of the isodityrosine cross-link</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Milani, M.</Author>
-<Author>Savard, P.-Y.</Author>
-<Author>Ouellet, H.</Author>
-<Author>Ascenzi, P.</Author>
-<Author>Guertin, M.</Author>
-<Author>Bolognesi, M.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, May 2003</Citation>
-<Description>Crystallographic structure of Mycobacterium tuberculosis hemoglobin O.</Description>
-<Xref>PDB:1NGK</Xref>
-<Note>X-ray diffraction, 2.11 angstroms</Note>
-</ReferenceBlock>
-<Comment>This cross-link can be produced as an oxidation artifact, or enzymatically by enzymes like myeloperoxidase. Since the enzymatic reaction proceeds by a free-radical mechanism, the cross-link can be aleatoric with 2, 3 or 4 tyrosines rings becoming linked in several possible ways.  See also RESID:AA0367.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>myeloperoxidase (EC 1.11.1.7)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>Y, Y</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Condition>secondary to RESID:AA0146</Condition>
-<Xref>GO:0030960</Xref>
-<Xref>PSI-MOD:00373</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>aleatoric crosslink</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__isodityrosine (tyr-tyr)__y__y">CROSSLNK Isodityrosine (Tyr-Tyr)</Feature>
-</Features>
-<Image src="/images/AA0368.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0368.PDB" />
-</Entry>
-<Entry id="AA0369">
-<Header>
-<Code>AA0369</Code>
-<Dates>
-<CreationDate>30-Jun-2004</CreationDate>
-<StrucRevDate>30-Jun-2004</StrucRevDate>
-<TextChngDate>24-Oct-2008</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>3,4-dihydroxy-L-arginine</Name>
-<AlternateName>2-amino-5-guanidino-3,4-dihydroxypentanoic acid</AlternateName>
-<AlternateName>beta,gamma-dihydroxyarginine</AlternateName>
-<SystematicName>(2S,3Xi,4Xi)-2-amino-5-carbamimidamido-3,4-dihydroxypentanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 12 N 4 O 3</Formula>
-<Weight type="chemical">188.19</Weight>
-<Weight type="physical">188.090940</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0002">
-<Formula>C 0 H 0 N 0 O 2</Formula>
-<Weight type="chemical">32.00</Weight>
-<Weight type="physical">31.989829</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Taylor, S.W.</Author>
-<Author>Craig, A.G.</Author>
-<Author>Fischer, W.H.</Author>
-<Author>Park, M.</Author>
-<Author>Lehrer, R.I.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 275, 38417-38426, 2000</Citation>
-<Title>Styelin D, an extensively modified antimicrobial peptide from ascidian hemocytes.</Title>
-<Xref>DOI:10.1074/jbc.M006762200</Xref>
-<Xref>PMID:10978343</Xref>
-</ReferenceBlock>
-<Comment>Hydroxylations at C-3 and C-4 are assumed. Neither the positions of the hydroxylations nor the stereochemistry for the chiral centers they produce have been determined. The (2S,3R,4R) stereoisomer is shown.</Comment>
-<SequenceCode>
-<SequenceSpec>R</SequenceSpec>
-<Xref>GO:0030961</Xref>
-<Xref>PSI-MOD:00374</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__3,4-dihydroxyarginine__r">MOD_RES 3,4-dihydroxyarginine</Feature>
-</Features>
-<Image src="/images/AA0369.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0369.PDB" />
-</Entry>
-<Entry id="AA0370">
-<Header>
-<Code>AA0370</Code>
-<Dates>
-<CreationDate>30-Jun-2004</CreationDate>
-<StrucRevDate>30-Jun-2004</StrucRevDate>
-<TextChngDate>30-Sep-2008</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>4,5-dihydroxy-L-lysine</Name>
-<AlternateName>alpha,epsilon-diamino-delta,gamma-dihydroxycaproic acid</AlternateName>
-<AlternateName>delta,gamma-dihydroxylysine</AlternateName>
-<SystematicName>(2S,4Xi,5Xi)-2,6-diamino-4,5-dihydroxyhexanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 12 N 2 O 3</Formula>
-<Weight type="chemical">160.17</Weight>
-<Weight type="physical">160.084792</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 0 H 0 N 0 O 2</Formula>
-<Weight type="chemical">32.00</Weight>
-<Weight type="physical">31.989829</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Taylor, S.W.</Author>
-<Author>Craig, A.G.</Author>
-<Author>Fischer, W.H.</Author>
-<Author>Park, M.</Author>
-<Author>Lehrer, R.I.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 275, 38417-38426, 2000</Citation>
-<Title>Styelin D, an extensively modified antimicrobial peptide from ascidian hemocytes.</Title>
-<Xref>DOI:10.1074/jbc.M006762200</Xref>
-<Xref>PMID:10978343</Xref>
-</ReferenceBlock>
-<Comment>Hydroxylations at C-4 and C-5 are assumed. Neither the positions of the hydroxylations nor the stereochemistry for the chiral centers they produce have been determined. The (2S,4R,5R) stereoisomer is shown.</Comment>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>GO:0030963</Xref>
-<Xref>PSI-MOD:00375</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__4,5-dihydroxylysine__k">MOD_RES 4,5-dihydroxylysine</Feature>
-</Features>
-<Image src="/images/AA0370.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0370.PDB" />
-</Entry>
-<Entry id="AA0371">
-<Header>
-<Code>AA0371</Code>
-<Dates>
-<CreationDate>30-Jul-2004</CreationDate>
-<StrucRevDate>30-Jul-2004</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>1'-(phospho-5'-adenosine)-L-histidine</Name>
-<AlternateName>L-histidine 5'-adenosine phosphoramidester</AlternateName>
-<AlternateName>L-histidine monoanhydride with 5'-adenylic acid</AlternateName>
-<AlternateName>N(tau)-5'-adenylic-L-histidine</AlternateName>
-<AlternateName>N1'-adenylylated histidine</AlternateName>
-<AlternateName>tele-5'-adenylic-L-histidine</AlternateName>
-<SystematicName>(2S)-2-amino-3-[1-(5'-adenosine phosphono)imidazol-4-yl]propanoic acid</SystematicName>
-<Xref>PDBHET:AMP</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 16 H 19 N 8 O 7 P 1</Formula>
-<Weight type="chemical">466.35</Weight>
-<Weight type="physical">466.111432</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0009">
-<Formula>C 10 H 12 N 5 O 6 P 1</Formula>
-<Weight type="chemical">329.21</Weight>
-<Weight type="physical">329.052520</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lima, C.D.</Author>
-<Author>Klein, M.G.</Author>
-<Author>Hendrickson, W.A.</Author>
-</Authors>
-<Citation>Science 278, 286-290, 1997</Citation>
-<Title>Structure-based analysis of catalysis and substrate definition in the HIT protein family.</Title>
-<Xref>DOI:10.1126/science.278.5336.286</Xref>
-<Xref>PMID:9323207</Xref>
-<Note>X-ray diffraction, 1.8 angstroms; chemical evidence for adenylyl phosphoramide intermediate</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Huang, K.</Author>
-<Author>Arabshahi, A.</Author>
-<Author>Wei, Y.</Author>
-<Author>Frey, P.A.</Author>
-</Authors>
-<Citation>Biochemistry 43, 7637-7642, 2004</Citation>
-<Title>The mechanism of action of the fragile histidine triad, Fhit: isolation of a covalent adenylyl enzyme and chemical rescue of H96G-Fhit.</Title>
-<Xref>DOI:10.1021/bi049762n</Xref>
-<Xref>PMID:15182206</Xref>
-<Note>chemical evidence for adenylyl phosphoramide intermediate</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>McCoy, J.G.</Author>
-<Author>Arabshahi, A.</Author>
-<Author>Bitto, E.</Author>
-<Author>Bingman, C.A.</Author>
-<Author>Ruzicka, F.J.</Author>
-<Author>Frey, P.A.</Author>
-<Author>Phillips Jr., G.N.</Author>
-</Authors>
-<Citation>Biochemistry 45, 3154-3162, 2006</Citation>
-<Title>Structure and mechanism of an ADP-glucose phosphorylase from Arabidopsis thaliana.</Title>
-<Xref>DOI:10.1021/bi052232m</Xref>
-<Xref>PMID:16519510</Xref>
-<Note>X-ray diffraction, 1.83 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>McCoy, J.G.</Author>
-<Author>Bitto, E.</Author>
-<Author>Phillips Jr., G.N.</Author>
-<Author>Bingman, C.A.</Author>
-<Author>Bingman, C.A.</Author>
-<Author>Center for Eukaryotic Structural Genomics (CESG)</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, March 2005</Citation>
-<Description>X-ray structure of GalTt-like protein from Arabidopsis thaliana At5g18200.</Description>
-<Xref>PDB:1Z84</Xref>
-<Note>X-ray diffraction, 1.83 angstroms, of the the trapped covalent intermediate</Note>
-</ReferenceBlock>
-<Comment>The phosphoramide bond is probably formed with the tele-nitrogen of histidine in most cases.</Comment>
-<SequenceCode>
-<SequenceSpec>H</SequenceSpec>
-<Xref>GO:0051111</Xref>
-<Xref>GO:0051112</Xref>
-<Xref>GO:0051113</Xref>
-<Xref>PSI-MOD:00376</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="act_site__tele-amp-histidine intermediate__h">ACT_SITE Tele-AMP-histidine intermediate</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="act_site__amp-histidine intermediate__h">ACT_SITE AMP-histidine intermediate</Feature>
-<Note>this UniProt feature is used when the isomeric structure has not been determined</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0371.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0371.PDB" />
-</Entry>
-<Entry id="AA0372">
-<Header>
-<Code>AA0372</Code>
-<Dates>
-<CreationDate>30-Jul-2004</CreationDate>
-<StrucRevDate>30-Jul-2004</StrucRevDate>
-<TextChngDate>31-Jul-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>1'-(phospho-5'-uridine)-L-histidine</Name>
-<AlternateName>L-histidine 5'-uridine phosphoramidester</AlternateName>
-<AlternateName>L-histidine monoanhydride with 5'-uridylic acid</AlternateName>
-<AlternateName>N(tau)-5'-uridylic-L-histidine</AlternateName>
-<AlternateName>N1'-uridylylated histidine</AlternateName>
-<AlternateName>tele-5'-uridylic-L-histidine</AlternateName>
-<SystematicName>(S)-2-amino-3-[1-(5'-uridine phosphono)imidazol-4-yl]propanoic acid</SystematicName>
-<Xref>PDBHET:U5P</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 15 H 18 N 5 O 9 P 1</Formula>
-<Weight type="chemical">443.31</Weight>
-<Weight type="physical">443.084214</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0009">
-<Formula>C 9 H 11 N 2 O 8 P 1</Formula>
-<Weight type="chemical">306.17</Weight>
-<Weight type="physical">306.025302</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wong, L.J.</Author>
-<Author>Sheu, K.F.</Author>
-<Author>Lee, S.L.</Author>
-<Author>Frey, P.A.</Author>
-</Authors>
-<Citation>Biochemistry 16, 1010-1016, 1977</Citation>
-<Title>Galactose-1-phosphate uridylyltransferase: isolation and properties of a uridylyl-enzyme intermediate.</Title>
-<Xref>DOI:10.1021/bi00624a032</Xref>
-<Xref>PMID:321007</Xref>
-<Note>chemical evidence for uridylyl phosphoramide intermediate</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yang, S.L.</Author>
-<Author>Frey, P.A.</Author>
-</Authors>
-<Citation>Biochemistry 18, 2980-2984, 1979</Citation>
-<Title>Nucleophile in the active site of Escherichia coli galactose-1-phosphate uridylyltransferase: degradation of the uridylyl-enzyme intermediate to N3-phosphohistidine.</Title>
-<Xref>DOI:10.1021/bi00581a011</Xref>
-<Xref>PMID:380639</Xref>
-<Note>chemical evidence for tele-nitrogen uridylyl phosphoramide intermediate; the 1'-nitrogen is called N(3)</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wedekind, J.E.</Author>
-<Author>Frey, P.A.</Author>
-<Author>Rayment, I.</Author>
-</Authors>
-<Citation>Biochemistry 35, 11560-11569, 1996</Citation>
-<Title>The structure of nucleotidylated histidine-166 of galactose-1-phosphate uridylyltransferase provides insight into phosphoryl group transfer.</Title>
-<Xref>DOI:10.1021/bi9612677</Xref>
-<Xref>PMID:8794735</Xref>
-<Note>X-ray diffraction, 1.86 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wedekind, J.E.</Author>
-<Author>Frey, P.A.</Author>
-<Author>Rayment, I.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, June 1996</Citation>
-<Description>The structure of nucleotidylated galactose-1-phosphate uridylyltransferase from Escherichia coli at 1.86 Angstroms resolution.</Description>
-<Xref>PDB:1HXQ</Xref>
-<Note>X-ray diffraction, 1.86 angstroms</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>H</SequenceSpec>
-<Xref>GO:0051110</Xref>
-<Xref>GO:0051114</Xref>
-<Xref>GO:0051115</Xref>
-<Xref>PSI-MOD:00377</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="act_site__tele-ump-histidine intermediate__h">ACT_SITE Tele-UMP-histidine intermediate</Feature>
-</Features>
-<Image src="/images/AA0372.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0372.PDB" />
-</Entry>
-<Entry id="AA0373">
-<Header>
-<Code>AA0373</Code>
-<Dates>
-<CreationDate>30-Sep-2004</CreationDate>
-<StrucRevDate>30-Sep-2004</StrucRevDate>
-<TextChngDate>30-Sep-2008</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-aspartyl aldehyde</Name>
-<AlternateName>L-aminosuccinaldehydic acid</AlternateName>
-<AlternateName>L-aminosuccinic acid semialdehyde</AlternateName>
-<AlternateName>L-aspartate-beta-semialdehyde</AlternateName>
-<AlternateName>L-aspartic beta-semialdehyde</AlternateName>
-<AlternateName>L-beta-formylalanine</AlternateName>
-<SystematicName>(S)-2-amino-4-oxobutanoic acid</SystematicName>
-<Xref>CAS:498-20-4</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 5 N 1 O 2</Formula>
-<Weight type="chemical">99.09</Weight>
-<Weight type="physical">99.032028</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0004">
-<Formula>C 0 H 0 N 0 O -1</Formula>
-<Weight type="chemical">-16.00</Weight>
-<Weight type="physical">-15.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Anderson, L.B.</Author>
-<Author>Ouellette, A.J.</Author>
-<Author>Eaton-Rye, J.</Author>
-<Author>Maderia, M.</Author>
-<Author>MacCoss, M.J.</Author>
-<Author>Yates 3rd, J.R.</Author>
-<Author>Barry, B.A.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 126, 8399-8405, 2004</Citation>
-<Title>Evidence for a post-translational modification, aspartyl aldehyde, in a photosynthetic membrane protein.</Title>
-<Xref>DOI:10.1021/ja0478781</Xref>
-<Xref>PMID:15237995</Xref>
-<Note>amine and hydrazine derivatization; chemical characterization and mass spectrometric identification</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>D</SequenceSpec>
-<Xref>GO:0051203</Xref>
-<Xref>PSI-MOD:00378</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="mod_res__aspartyl aldehyde__d">MOD_RES Aspartyl aldehyde</Feature>
-</Features>
-<Image src="/images/AA0373.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0373.PDB" />
-</Entry>
-<Entry id="AA0374">
-<Header>
-<Code>AA0374</Code>
-<Dates>
-<CreationDate>22-Oct-2004</CreationDate>
-<StrucRevDate>22-Oct-2004</StrucRevDate>
-<TextChngDate>05-Dec-2008</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-serine microcin E492 siderophore ester</Name>
-<SystematicName>N-[5-(6-O-seryl-beta-glucosyl)-2,3-dihydroxybenzoyl]-O-[N-(2,3-dihydroxybenzoyl)-O-[N-(2,3-dihydroxybenzoyl)seryl]seryl]serine</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 39 H 43 N 4 O 23</Formula>
-<Weight type="chemical">935.78</Weight>
-<Weight type="physical">935.231809</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 36 H 37 N 3 O 20</Formula>
-<Weight type="chemical">831.69</Weight>
-<Weight type="physical">831.197041</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Thomas, X.</Author>
-<Author>Destoumieux-Garzón, D.</Author>
-<Author>Peduzzi, J.</Author>
-<Author>Afonso, C.</Author>
-<Author>Blond, A.</Author>
-<Author>Birlirakis, N.</Author>
-<Author>Goulard, C.</Author>
-<Author>Dubost, L.</Author>
-<Author>Thai, R.</Author>
-<Author>Tabet, J.C.</Author>
-<Author>Rebuffat, S.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 279, 28233-28242, 2004</Citation>
-<Title>Siderophore peptide, a new type of post-translationally modified antibacterial peptide with potent activity.</Title>
-<Xref>DOI:10.1074/jbc.M400228200</Xref>
-<Xref>PMID:15102848</Xref>
-<Note>mass spectrometric, (1)H-NMR, and (13)C-NMR identification; the encoding of an author's name in the PubMed citation is corrected to UTF8</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Nolan, E.M.</Author>
-<Author>Walsh, C.T.</Author>
-</Authors>
-<Citation>Biochemistry 47, 9289-9299, 2008</Citation>
-<Title>Investigations of the MceIJ-catalyzed posttranslational modification of the microcin E492 C-terminus: linkage of ribosomal and nonribosomal peptides to form &#x201c;trojan horse&#x201d; antibiotics.</Title>
-<Xref>DOI:10.1021/bi800826j</Xref>
-<Xref>PMID:18690711</Xref>
-<Note>biosynthesis</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0051263</Xref>
-<Xref>PSI-MOD:00379</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__serine microcin e492 siderophore ester__s">MOD_RES Serine microcin E492 siderophore ester</Feature>
-</Features>
-<Image src="/images/AA0374.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0374.PDB" />
-</Entry>
-<Entry id="AA0375">
-<Header>
-<Code>AA0375</Code>
-<Dates>
-<CreationDate>12-Nov-2004</CreationDate>
-<StrucRevDate>12-Nov-2004</StrucRevDate>
-<TextChngDate>31-Mar-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-aspartyl molybdenum bis(molybdopterin guanine dinucleotide)</Name>
-<AlternateName>2-amino-5,6-dimercapto-7-methyl-3,7,8a,9-tetrahydro-8-oxa-1,3,9,10-tetraazaanthracen-4-one guanosine dinucleotide</AlternateName>
-<AlternateName>nitrate reductase A aspartyl Mo-bisMGD cofactor</AlternateName>
-<AlternateName>phosphoric acid 4-(2-amino-4-oxo-3,4,5,6,-tetrahydro-pteridin-6-yl)-2-hydroxy-3,4-dimercapto-but-3-en-yl ester guanylate ester</AlternateName>
-<SystematicName>bis[8-amino-1a,2,4a,5,6,7,10-heptahydro-2-(trihydrogen diphosphate 5'-ester with guanosine)methyl-6-oxo-3,4-disulfanyl-pteridino[6,7-5,6]pyranoato-S3,S4]-aspartyl-molybdenum</SystematicName>
-<Xref>PDBHET:MGD</Xref>
-<Xref>PDBHET:MO</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 44 H 52 Mo 1 N 21 O 29 P 4 S 4</Formula>
-<Weight type="chemical">1687.10</Weight>
-<Weight type="physical">1688.012718</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0004">
-<Formula>C 40 H 47 Mo 1 N 20 O 26 P 4 S 4</Formula>
-<Weight type="chemical">1572.02</Weight>
-<Weight type="physical">1572.985775</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bertero, M.G.</Author>
-<Author>Rothery, R.A.</Author>
-<Author>Palak, M.</Author>
-<Author>Hou, C.</Author>
-<Author>Lim, D.</Author>
-<Author>Blasco, F.</Author>
-<Author>Weiner, J.H.</Author>
-<Author>Strynadka, N.C.J.</Author>
-</Authors>
-<Citation>Nature Struct. Biol. 10, 681-687, 2003</Citation>
-<Title>Insights into the respiratory electron transfer pathway from the structure of nitrate reductase A.</Title>
-<Xref>DOI:10.1038/nsb969</Xref>
-<Xref>PMID:12910261</Xref>
-<Note>X-ray diffraction, 1.90 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bertero, M.G.</Author>
-<Author>Strynadka, N.C.J.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, July 2003</Citation>
-<Description>Crystal structure of nitrate reductase A, NarGHI, from Escherichia coli.</Description>
-<Xref>PDB:1Q16</Xref>
-<Note>X-ray diffraction, 1.90 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Jormakka, M.</Author>
-<Author>Richardson, D.</Author>
-<Author>Byrne, B.</Author>
-<Author>Iwata, S.</Author>
-</Authors>
-<Citation>Structure 12, 95-104, 2004</Citation>
-<Title>Architecture of NarGH reveals a structural classification of Mo-bisMGD enzymes.</Title>
-<Xref>DOI:10.1016/j.str.2003.11.020</Xref>
-<Xref>PMID:14725769</Xref>
-<Note>X-ray diffraction, 2.00 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Jormakka, M.</Author>
-<Author>Richardson, D.</Author>
-<Author>Byrne, B.</Author>
-<Author>Iwata, S.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, September 2003</Citation>
-<Description>Crystal structure of NarGH complex.</Description>
-<Xref>PDB:1R27</Xref>
-<Note>X-ray diffraction, 2.00 angstroms</Note>
-</ReferenceBlock>
-<Comment>One possible structure of a reduced form (+4H) is shown. The fully reduced form would be 1a,2,3,4,4a,5,6,7,10-nonahydro. The fully oxidized form would be 2,6,7-trihydro.</Comment>
-<Comment>The model is based on the structure of 1Q16 in which one of the molybdopterin ring systems is in the tricyclic form, and the other is in a bicyclic form with an opened pyran ring.</Comment>
-<SequenceCode>
-<SequenceSpec>D</SequenceSpec>
-<Xref>GO:0051217</Xref>
-<Xref>PSI-MOD:00380</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>metalloprotein</Keyword>
-<Keyword>molybdenum</Keyword>
-<Keyword>molybdopterin</Keyword>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt" key="metal__molybdenum__d">METAL Molybdenum</Feature>
-<Note>this UniProt feature has a structural misrepresentation</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0375.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0375.PDB" />
-</Entry>
-<Entry id="AA0376">
-<Header>
-<Code>AA0376</Code>
-<Dates>
-<CreationDate>12-Nov-2004</CreationDate>
-<StrucRevDate>12-Nov-2004</StrucRevDate>
-<TextChngDate>31-Mar-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-selenocysteinyl tungsten bis(molybdopterin guanine dinucleotide)</Name>
-<AlternateName>2-amino-5,6-dimercapto-7-methyl-3,7,8a,9-tetrahydro-8-oxa-1,3,9,10-tetraazaanthracen-4-one guanosine dinucleotide</AlternateName>
-<AlternateName>formate dehydrogenase selenocysteine W-bisMGD cofactor</AlternateName>
-<AlternateName>guanylate-O'-phosphoric acid mono-(2-amino-5,6-dimercapto-4-oxo-3,5,6,7,8a,9,10,10a-octahydro-4h-8-oxa-1,3,9,10-tetraaza-anthracen-7-ylmethyl) ester</AlternateName>
-<SystematicName>bis[8-amino-1a,2,4a,5,6,7,10-heptahydro-2-(trihydrogen diphosphate 5'-ester with guanosine)methyl-6-oxo-3,4-disulfanyl-pteridino[6,7-5,6]pyranoato-S3,S4]-selenocysteinyl-Se-tungsten sulfide</SystematicName>
-<Xref>PDBHET:2MD</Xref>
-<Xref>PDBHET:MGD</Xref>
-<Xref>PDBHET:W</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 43 H 52 N 21 O 27 P 4 S 5 Se 1 W 1</Formula>
-<Weight type="chemical">1842.02</Weight>
-<Weight type="physical">1841.957004</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005" label="CYS">
-<Formula>C 40 H 47 N 20 O 26 P 4 S 4 Se 1 W 1</Formula>
-<Weight type="chemical">1738.88</Weight>
-<Weight type="physical">1738.947820</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0022" label="SEC">
-<Formula>C 40 H 47 N 20 O 26 P 4 S 5 Se 0 W 1</Formula>
-<Weight type="chemical">1691.97</Weight>
-<Weight type="physical">1691.003369</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Raaijmakers, H.</Author>
-<Author>Teixeira, S.</Author>
-<Author>Dias, J.M.</Author>
-<Author>Almendra, M.J.</Author>
-<Author>Brondino, C.D.</Author>
-<Author>Moura, I.</Author>
-<Author>Moura, J.J.G.</Author>
-<Author>Romao, M.J.</Author>
-</Authors>
-<Citation>J. Biol. Inorg. Chem. 6, 398-404, 2001</Citation>
-<Title>Tungsten-containing formate dehydrogenase from Desulfovibrio gigas: metal identification and preliminary structural data by multi-wavelength crystallography.</Title>
-<Xref>DOI:10.1007/s007750100215</Xref>
-<Xref>PMID:11372198</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Raaijmakers, H.</Author>
-<Author>Macieira, S.</Author>
-<Author>Dias, J.M.</Author>
-<Author>Teixeira, S.</Author>
-<Author>Bursakov, S.</Author>
-<Author>Huber, R.</Author>
-<Author>Moura, J.J.G.</Author>
-<Author>Moura, I.</Author>
-<Author>Romao, M.J.</Author>
-</Authors>
-<Citation>Structure 10, 1261-1272, 2002</Citation>
-<Title>Gene sequence and the 1.8 A crystal structure of the tungsten-containing formate dehydrogenase from Desulfovibrio gigas.</Title>
-<Xref>DOI:10.1016/S0969-2126(02)00826-2</Xref>
-<Xref>PMID:12220497</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Raaijmakers, H.C.A.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, June 2002</Citation>
-<Description>Tungsten containing formate dehydrogenase from Desulfovibrio gigas.</Description>
-<Xref>PDB:1H0H</Xref>
-<Note>X-ray diffraction, 1.8 angstroms</Note>
-</ReferenceBlock>
-<Comment>One possible structure of a reduced form (+4H) is shown. The fully reduced form would be 1a,2,3,4,4a,5,6,7,10-nonahydro. The fully oxidized form would be 2,6,7-trihydro.</Comment>
-<SequenceCode link="CYS">
-<SequenceSpec>C</SequenceSpec>
-<Condition>secondary to RESID:AA0022</Condition>
-<Xref>GO:0051218</Xref>
-<Xref>PSI-MOD:01469</Xref>
-</SequenceCode>
-<SequenceCode link="SEC">
-<SequenceSpec>U</SequenceSpec>
-<Xref>PSI-MOD:00381</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>metalloprotein</Keyword>
-<Keyword>molybdopterin</Keyword>
-<Keyword>phosphoprotein</Keyword>
-<Keyword>selenium</Keyword>
-<Keyword>selenocysteine</Keyword>
-<Keyword>tungsten</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt" key="metal__tungsten__c">METAL Tungsten</Feature>
-<Note>this UniProt feature has a structural misrepresentation</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0376.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0376.PDB" />
-</Entry>
-<Entry id="AA0377">
-<Header>
-<Code>AA0377</Code>
-<Dates>
-<CreationDate>31-Dec-2004</CreationDate>
-<StrucRevDate>31-Dec-2004</StrucRevDate>
-<TextChngDate>24-Oct-2008</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>3-(2-methylthio)ethyl-6-(4-hydroxybenzylidene)-5-iminopiperazin-2-one</Name>
-<AlternateName>3-(2-methylthio)ethyl-6-(4-hydroxybenzylidene)-5-amino-3,6-didehydropyrazin-2-ol</AlternateName>
-<AlternateName>GFP-like chromoprotein asFP595 chromophore</AlternateName>
-<AlternateName>L-methionyl-L-tyrosyl-2-keto-5-iminopiperazine</AlternateName>
-<SystematicName>3-(2-methylsulfanyl)ethyl-6-(4-hydroxybenzylidene)-5-iminopiperazin-2-one</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 14 H 15 N 2 O 2 S 1</Formula>
-<Weight type="chemical">275.35</Weight>
-<Weight type="physical">275.085424</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0013 AA0019">
-<Formula>C 0 H -4 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-20.03</Weight>
-<Weight type="physical">-20.026215</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lukyanov, K.A.</Author>
-<Author>Fradkov, A.F.</Author>
-<Author>Gurskaya, N.G.</Author>
-<Author>Matz, M.V.</Author>
-<Author>Labas, Y.A.</Author>
-<Author>Savitsky, A.P.</Author>
-<Author>Markelov, M.L.</Author>
-<Author>Zaraisky, A.G.</Author>
-<Author>Zhao, X.</Author>
-<Author>Fang, Y.</Author>
-<Author>Tan, W.</Author>
-<Author>Lukyanov, S.A.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 275, 25879-25882, 2000</Citation>
-<Title>Natural animal coloration can be determined by a nonfluorescent green fluorescent protein homolog.</Title>
-<Xref>DOI:10.1074/jbc.C000338200</Xref>
-<Xref>PMID:10852900</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Martynov, V.I.</Author>
-<Author>Savitsky, A.P.</Author>
-<Author>Martynova, N.Y.</Author>
-<Author>Savitsky, P.A.</Author>
-<Author>Lukyanov, K.A.</Author>
-<Author>Lukyanov, S.A.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 276, 21012-21016, 2001</Citation>
-<Title>Alternative cyclization in GFP-like proteins family. The formation and structure of the chromophore of a purple chromoprotein from Anemonia sulcata.</Title>
-<Xref>DOI:10.1074/jbc.M100500200</Xref>
-<Xref>PMID:11259412</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Zagranichny, V.E.</Author>
-<Author>Rudenko, N.V.</Author>
-<Author>Gorokhovatsky, A.Y.</Author>
-<Author>Zakharov, M.V.</Author>
-<Author>Balashova, T.A.</Author>
-<Author>Arseniev, A.S.</Author>
-</Authors>
-<Citation>Biochemistry 43, 13598-13603, 2004</Citation>
-<Title>Traditional GFP-type cyclization and unexpected fragmentation site in a purple chromoprotein from Anemonia sulcata, asFP595.</Title>
-<Xref>DOI:10.1021/bi0488247</Xref>
-<Xref>PMID:15491166</Xref>
-</ReferenceBlock>
-<Comment>The correct structure for the asFP595 chromophore is now thought to be a para-hydroxybenzylidene-5-imidazolidinone. See RESID:AA0379.</Comment>
-<Comment>The diagram presents structures for two tautomeric forms with the glycine, which is linked by either an imino or amino group, shown in gray. In the correct structure, the glycine amino group forms part of a 5-member ring.</Comment>
-<SequenceCode>
-<SequenceSpec>M, Y</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Condition>carboxamidine</Condition>
-<Condition>cross-link 1</Condition>
-<Xref>GO:0051357</Xref>
-<Xref>PSI-MOD:00382</Xref>
-</SequenceCode>
-<Source>deprecated</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this dubious modification is not currently annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0377.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0377.PDB" />
-</Entry>
-<Entry id="AA0378">
-<Header>
-<Code>AA0378</Code>
-<Dates>
-<CreationDate>31-Dec-2004</CreationDate>
-<StrucRevDate>31-Dec-2004</StrucRevDate>
-<TextChngDate>20-May-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>2-imino-glutamic acid 5-imidazolinone glycine</Name>
-<AlternateName>2,N-didehydroglutamyl-5-imidazolinone glycine</AlternateName>
-<AlternateName>2-(3-carboxy-1-iminopropyl)-1-carboxymethyl-1-imidazolin-5-one</AlternateName>
-<AlternateName>2-imino-glutamyl-5-imidazolinone glycine</AlternateName>
-<AlternateName>para-hydroxybenzylidene-imidazolidinone chromophore</AlternateName>
-<AlternateName>[2-(3-carboxy-1-iminopropyl)-5-oxo-4,5-dihydro-imidazol-1-yl]-acetic acid</AlternateName>
-<SystematicName>4-[1-(carboxymethyl)-5-oxo-4,5-dihydro-1H-imidazol-2-yl]-4-iminobutanoic acid</SystematicName>
-<Xref>PDBHET:CRU</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 6 N 2 O 3</Formula>
-<Weight type="chemical">166.14</Weight>
-<Weight type="physical">166.037842</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0006 AA0008">
-<Formula>C 0 H -4 N 0 O -1</Formula>
-<Weight type="chemical">-20.03</Weight>
-<Weight type="physical">-20.026215</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gurskaya, N.G.</Author>
-<Author>Fradkov, A.F.</Author>
-<Author>Terskikh, A.</Author>
-<Author>Matz, M.V.</Author>
-<Author>Labas, Y.A.</Author>
-<Author>Martynov, V.I.</Author>
-<Author>Yanushevich, Y.G.</Author>
-<Author>Lukyanov, K.A.</Author>
-<Author>Lukyanov, S.A.</Author>
-</Authors>
-<Citation>FEBS Lett. 507, 16-20, 2001</Citation>
-<Title>GFP-like chromoproteins as a source of far-red fluorescent proteins.</Title>
-<Xref>DOI:10.1016/S0014-5793(01)02930-1</Xref>
-<Xref>PMID:11682051</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wilmann, P.G.</Author>
-<Author>Petersen, J.</Author>
-<Author>Pettikiriarachchi, A.</Author>
-<Author>Buckle, A.M.</Author>
-<Author>Smith, S.C.</Author>
-<Author>Olsen, S.</Author>
-<Author>Perugini, M.A.</Author>
-<Author>Devenish, R.J.</Author>
-<Author>Prescott, M.</Author>
-<Author>Rossjohn, J.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 349, 223-237, 2005</Citation>
-<Title>The 2.1A crystal structure of the far-red fluorescent protein HcRed: inherent conformational flexibility of the chromophore.</Title>
-<Xref>DOI:10.1016/j.jmb.2005.03.020</Xref>
-<Xref>PMID:15876379</Xref>
-<Note>spectrofluorimetric analysis; X-ray diffraction, 2.10 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wilmann, P.G.</Author>
-<Author>Petersen, J.</Author>
-<Author>Pettikiriarachchi, A.</Author>
-<Author>Buckle, A.M.</Author>
-<Author>Devenish, R.J.</Author>
-<Author>Prescott, M.</Author>
-<Author>Rossjohn, J.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, February 2005</Citation>
-<Description>The 2.1A crystal structure of the far-red fluorescent protein HcRed: inherent conformational flexibility of the chromophore.</Description>
-<Xref>PDB:1YZW</Xref>
-<Note>X-ray diffraction, 2.10 angstroms</Note>
-</ReferenceBlock>
-<Comment>This entry represents the cross-link of the peptide backbone from the alpha-carboxyl carbon of residue N, a glutamic acid, to the alpha-amino nitrogen of residue N+2, a glycine, coupled with the formation of a double bond to the alpha-amino nitrogen of residue N, and the loss of a molecule of water.</Comment>
-<Comment>This cross-link is accompanied by modification of residue N+1. The modified residue N+1 is presented in a separate entry and is not included in the mass accounting of this entry. The backbone atoms of residue N+1 are shown in gray in the diagram.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>E, G</SequenceSpec>
-<Condition>carboxamidine</Condition>
-<Condition>cross-link 1</Condition>
-<Condition>incidental to RESID:AA0183</Condition>
-<Condition>incidental to RESID:AA0365</Condition>
-<Xref>GO:0051358</Xref>
-<Xref>PSI-MOD:00383</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>chromoprotein</Keyword>
-<Keyword>imidazolinone/oxazolinone ring</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__2-iminomethyl-5-imidazolinone (glu-gly)__e__g">CROSSLNK 2-iminomethyl-5-imidazolinone (Glu-Gly)</Feature>
-</Features>
-<Image src="/images/AA0378.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0378.PDB" />
-</Entry>
-<Entry id="AA0379">
-<Header>
-<Code>AA0379</Code>
-<Dates>
-<CreationDate>31-Dec-2004</CreationDate>
-<StrucRevDate>31-Dec-2004</StrucRevDate>
-<TextChngDate>20-May-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>2-imino-methionine 5-imidazolinone glycine</Name>
-<AlternateName>(2-[1-imino-3-(methylsulfanyl)propyl]-5-oxo-4,5-dihydro-imidazol-1-yl)acetic acid</AlternateName>
-<AlternateName>2,N-didehydromethionyl-5-imidazolinone glycine</AlternateName>
-<AlternateName>2-imino-methionyl-5-imidazolinone glycine</AlternateName>
-<AlternateName>2-[1-imino-3-(methylsulfanyl)propyl]-1-carboxymethyl-1-imidazolin-5-one</AlternateName>
-<AlternateName>GFP-like chromoprotein asFP595 chromophore</AlternateName>
-<AlternateName>para-hydroxybenzylidene-imidazolidinone chromophore</AlternateName>
-<AlternateName>red fluorescent protein eqFP611 chromophore</AlternateName>
-<SystematicName>(2-[3-(methylsulfanyl)propanimidoyl]-5-oxo-4,5-dihydro-1H-imidazol-1-yl)acetic acid</SystematicName>
-<Xref>PDBHET:NRQ</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 8 N 2 O 1 S 1</Formula>
-<Weight type="chemical">168.21</Weight>
-<Weight type="physical">168.035734</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0008 AA0013">
-<Formula>C 0 H -4 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-20.03</Weight>
-<Weight type="physical">-20.026215</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lukyanov, K.A.</Author>
-<Author>Fradkov, A.F.</Author>
-<Author>Gurskaya, N.G.</Author>
-<Author>Matz, M.V.</Author>
-<Author>Labas, Y.A.</Author>
-<Author>Savitsky, A.P.</Author>
-<Author>Markelov, M.L.</Author>
-<Author>Zaraisky, A.G.</Author>
-<Author>Zhao, X.</Author>
-<Author>Fang, Y.</Author>
-<Author>Tan, W.</Author>
-<Author>Lukyanov, S.A.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 275, 25879-25882, 2000</Citation>
-<Title>Natural animal coloration can be determined by a nonfluorescent green fluorescent protein homolog.</Title>
-<Xref>DOI:10.1074/jbc.C000338200</Xref>
-<Xref>PMID:10852900</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wiedenmann, J.</Author>
-<Author>Schenk, A.</Author>
-<Author>Roecker, C.</Author>
-<Author>Girod, A.</Author>
-<Author>Spindler, K.-D.</Author>
-<Author>Nienhaus, G.U.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 99, 11646-11651, 2002</Citation>
-<Title>A far-red fluorescent protein with fast maturation and reduced oligomerization tendency from Entacmaea quadricolor (Anthozoa, Actinaria).</Title>
-<Xref>DOI:10.1073/pnas.182157199</Xref>
-<Xref>PMID:12185250</Xref>
-<Note>the punctuation of "Spindler, K.D." in the PubMed citation is corrected</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Petersen, J.</Author>
-<Author>Wilmann, P.G.</Author>
-<Author>Beddoe, T.</Author>
-<Author>Oakley, A.J.</Author>
-<Author>Devenish, R.J.</Author>
-<Author>Prescott, M.</Author>
-<Author>Rossjohn, J.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 278, 44626-44631, 2003</Citation>
-<Title>The 2.0-A crystal structure of eqFP611, a far red fluorescent protein from the sea anemone Entacmaea quadricolor.</Title>
-<Xref>DOI:10.1074/jbc.M307896200</Xref>
-<Xref>PMID:12909624</Xref>
-<Note>X-ray diffraction, 2.00 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Petersen, J.</Author>
-<Author>Wilmann, P.G.</Author>
-<Author>Beddoe, T.</Author>
-<Author>Oakley, A.J.</Author>
-<Author>Devenish, R.J.</Author>
-<Author>Prescott, M.</Author>
-<Author>Rossjohn, J.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, July 2003</Citation>
-<Description>The 2.0 crystal structure of eqFP611, a far-red fluorescent protein from the sea anemone Entacmaea quadricolor.</Description>
-<Xref>PDB:1UIS</Xref>
-<Note>X-ray diffraction, 2.00 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wilmann, P.G.</Author>
-<Author>Petersen, J.</Author>
-<Author>Devenish, R.J.</Author>
-<Author>Prescott, M.</Author>
-<Author>Rossjohn, J.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 280, 2401-2404, 2005</Citation>
-<Title>Variations on the GFP chromophore: A polypeptide fragmentation within the chromophore revealed in the 2.1-A crystal structure of a nonfluorescent chromoprotein from Anemonia sulcata.</Title>
-<Xref>DOI:10.1074/jbc.C400484200</Xref>
-<Xref>PMID:15542608</Xref>
-<Note>X-ray diffraction, 2.10 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Petersen, J.</Author>
-<Author>Wilmann, P.G.</Author>
-<Author>Beddoe, T.</Author>
-<Author>Oakley, A.J.</Author>
-<Author>Devenish, R.J.</Author>
-<Author>Prescott, M.</Author>
-<Author>Rossjohn, J.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, October 2004</Citation>
-<Description>Variations on the GFP chromophore: A fragmented 5-membered heterocycle revealed in the 2.1A crystal structure of a non-fluorescent chromoprotein.</Description>
-<Xref>PDB:1XQM</Xref>
-<Note>X-ray diffraction, 2.10 angstroms</Note>
-</ReferenceBlock>
-<Comment>This entry represents the cross-link of the peptide backbone from the alpha-carboxyl carbon of residue N, a methionine, to the alpha-amino nitrogen of residue N+2, a glycine, coupled with the formation of a double bond to the alpha-amino nitrogen of residue N, and the loss of a molecule of water.</Comment>
-<Comment>This cross-link is accompanied by modification of residue N+1. The modified residue N+1 is presented in a separate entry and is not included in the mass accounting of this entry. The backbone atoms of residue N+1 are shown in gray in the diagram.</Comment>
-<Comment>In the asFP595 chromoprotein, the peptide chain is cleaved at the methionine alpha-amino. For a previously proposed structure of the asFP595 chromoprotein, see RESID:AA0377.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>G, M</SequenceSpec>
-<Condition>carboxamidine</Condition>
-<Condition>cross-link 1</Condition>
-<Condition>incidental to RESID:AA0183</Condition>
-<Condition>incidental to RESID:AA0365</Condition>
-<Xref>GO:0051359</Xref>
-<Xref>PSI-MOD:00384</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chromoprotein</Keyword>
-<Keyword>imidazolinone/oxazolinone ring</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__2-iminomethyl-5-imidazolinone (met-gly)__m__g">CROSSLNK 2-iminomethyl-5-imidazolinone (Met-Gly)</Feature>
-</Features>
-<Image src="/images/AA0379.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0379.PDB" />
-</Entry>
-<Entry id="AA0380">
-<Header>
-<Code>AA0380</Code>
-<Dates>
-<CreationDate>31-Dec-2004</CreationDate>
-<StrucRevDate>31-Dec-2004</StrucRevDate>
-<TextChngDate>20-May-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-asparagine 5-imidazolinone glycine</Name>
-<AlternateName>2-[(S)-1,3-diamino-3-oxopropyl]-1-carboxymethyl-1-imidazolin-5-one</AlternateName>
-<AlternateName>asparaginyl-5-imidazolinone glycine</AlternateName>
-<AlternateName>para-hydroxybenzylidene-imidazolidinone chromophore</AlternateName>
-<AlternateName>Zoanthus sp. fluorescent protein FP506 chromophore</AlternateName>
-<AlternateName>[2-(1,3-diamino-3-oxopropyl)-5-oxo-4,5-dihydro-imidazol-1-yl]-acetic acid</AlternateName>
-<SystematicName>(2-[(1S)-1,3-diamino-3-oxopropyl]-5-oxo-4,5-dihydro-1H-imidazol-1-yl)acetic acid</SystematicName>
-<Xref>PDBHET:NYG</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 7 N 3 O 2</Formula>
-<Weight type="chemical">153.14</Weight>
-<Weight type="physical">153.053826</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0003 AA0008">
-<Formula>C 0 H -2 N 0 O -1</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Matz, M.V.</Author>
-<Author>Fradkov, A.F.</Author>
-<Author>Labas, Y.A.</Author>
-<Author>Savitsky, A.P.</Author>
-<Author>Zaraisky, A.G.</Author>
-<Author>Markelov, M.L.</Author>
-<Author>Lukyanov, S.A.</Author>
-</Authors>
-<Citation>Nature Biotechnol. 17, 969-973, 1999</Citation>
-<Title>Fluorescent proteins from nonbioluminescent Anthozoa species.</Title>
-<Xref>DOI:10.1038/13657</Xref>
-<Xref>PMID:10504696</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Pletneva, N.</Author>
-<Author>Pletnev, V.</Author>
-<Author>Tikhonova, T.</Author>
-<Author>Pakhomov, A.A.</Author>
-<Author>Popov, V.</Author>
-<Author>Martynov, V.I.</Author>
-<Author>Wlodawer, A.</Author>
-<Author>Dauter, Z.</Author>
-<Author>Pletnev, S.</Author>
-</Authors>
-<Citation>Acta Crystallogr. D Biol. Crystallogr. 63, 1082-1093, 2007</Citation>
-<Title>Refined crystal structures of red and green fluorescent proteins from the button polyp Zoanthus.</Title>
-<Xref>DOI:10.1107/S0907444907042461</Xref>
-<Xref>PMID:17881826</Xref>
-<Note>X-ray diffraction, 2.20 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Pletneva, N.</Author>
-<Author>Pletnev, V.</Author>
-<Author>Tikhonova, T.</Author>
-<Author>Pletnev, S.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, January 2007</Citation>
-<Description>Crystal structures of green fluorescent proteins from Zoanthus sp. at 2.2 A resolution.</Description>
-<Xref>PDB:2OJK</Xref>
-<Note>X-ray diffraction, 2.20 angstroms</Note>
-</ReferenceBlock>
-<Comment>This entry represents the cross-link of the peptide backbone from the alpha-carboxyl carbon of residue N, an asparagine, to the alpha-amino nitrogen of residue N+2, a glycine, coupled with the formation of a double bond to the alpha-amino nitrogen of residue N+1 which loses one hydrogen, and the loss of a molecule of water.</Comment>
-<Comment>This cross-link is accompanied by modification of residue N+1. The modified residue N+1 is presented in a separate entry and is not included in the mass accounting of this entry. The backbone atoms of residue N+1 are shown in gray in the diagram.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>G, N</SequenceSpec>
-<Condition>carboxamidine</Condition>
-<Condition>cross-link 1</Condition>
-<Condition>incidental to RESID:AA0183</Condition>
-<Condition>incidental to RESID:AA0365</Condition>
-<Xref>GO:0051360</Xref>
-<Xref>PSI-MOD:00385</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>chromoprotein</Keyword>
-<Keyword>imidazolinone/oxazolinone ring</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__5-imidazolinone (asn-gly)__n__g">CROSSLNK 5-imidazolinone (Asn-Gly)</Feature>
-</Features>
-<Image src="/images/AA0380.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0380.PDB" />
-</Entry>
-<Entry id="AA0381">
-<Header>
-<Code>AA0381</Code>
-<Dates>
-<CreationDate>31-Dec-2004</CreationDate>
-<StrucRevDate>31-Dec-2004</StrucRevDate>
-<TextChngDate>20-May-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-lysine 5-imidazolinone glycine</Name>
-<AlternateName>2-[(S)-1,5-diaminopentanyl]-1-carboxymethyl-1-imidazolin-5-one</AlternateName>
-<AlternateName>Anemonia majano fluorescent protein FP486 chromophore</AlternateName>
-<AlternateName>lysyl-5-imidazolinone glycine</AlternateName>
-<AlternateName>para-hydroxybenzylidene-imidazolidinone chromophore</AlternateName>
-<AlternateName>[2-(1,5-diaminopentanyl)-5-oxo-4,5-dihydro-imidazol-1-yl]-acetic acid</AlternateName>
-<SystematicName>(2-[(1S)-1,5-diaminopentyl]-5-oxo-4,5-dihydro-1H-imidazol-1-yl)acetic acid</SystematicName>
-<Xref>PDBHET:CR7</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 8 H 13 N 3 O 1</Formula>
-<Weight type="chemical">167.21</Weight>
-<Weight type="physical">167.105862</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012 AA0008">
-<Formula>C 0 H -2 N 0 O -1</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Matz, M.V.</Author>
-<Author>Fradkov, A.F.</Author>
-<Author>Labas, Y.A.</Author>
-<Author>Savitsky, A.P.</Author>
-<Author>Zaraisky, A.G.</Author>
-<Author>Markelov, M.L.</Author>
-<Author>Lukyanov, S.A.</Author>
-</Authors>
-<Citation>Nature Biotechnol. 17, 969-973, 1999</Citation>
-<Title>Fluorescent proteins from nonbioluminescent Anthozoa species.</Title>
-<Xref>DOI:10.1038/13657</Xref>
-<Xref>PMID:10504696</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Henderson, J.N.</Author>
-<Author>Remington, S.J.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 102, 12712-12717, 2005</Citation>
-<Title>Crystal structures and mutational analysis of amFP486, a cyan fluorescent protein from Anemonia majano.</Title>
-<Xref>DOI:10.1073/pnas.0502250102</Xref>
-<Xref>PMID:16120682</Xref>
-<Note>spectrofluorimetric analysis; X-ray diffraction, 1.65 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Henderson, J.N.</Author>
-<Author>Remington, S.J.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, June 2005</Citation>
-<Description>Crystal structures of amFP486, a cyan fluorescent protein from Anemonia majano, and variants.</Description>
-<Xref>PDB:2A46</Xref>
-<Note>X-ray diffraction, 1.65 angstroms</Note>
-</ReferenceBlock>
-<Comment>This entry represents the cross-link of the peptide backbone from the alpha-carboxyl carbon of residue N, a lysine, to the alpha-amino nitrogen of residue N+2, a glycine, coupled with the formation of a double bond to the alpha-amino nitrogen of residue N+1 which loses one hydrogen, and the loss of a molecule of water.</Comment>
-<Comment>This cross-link is accompanied by modification of residue N+1. The modified residue N+1 is presented in a separate entry and is not included in the mass accounting of this entry. The backbone atoms of residue N+1 are shown in gray in the diagram.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>G, K</SequenceSpec>
-<Condition>carboxamidine</Condition>
-<Condition>cross-link 1</Condition>
-<Condition>incidental to RESID:AA0183</Condition>
-<Condition>incidental to RESID:AA0365</Condition>
-<Xref>GO:0051361</Xref>
-<Xref>PSI-MOD:00386</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>chromoprotein</Keyword>
-<Keyword>imidazolinone/oxazolinone ring</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__5-imidazolinone (lys-gly)__k__g">CROSSLNK 5-imidazolinone (Lys-Gly)</Feature>
-</Features>
-<Image src="/images/AA0381.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0381.PDB" />
-</Entry>
-<Entry id="AA0382">
-<Header>
-<Code>AA0382</Code>
-<Dates>
-<CreationDate>25-Feb-2005</CreationDate>
-<StrucRevDate>25-Feb-2005</StrucRevDate>
-<TextChngDate>30-Jun-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>2-tetrahydropyridinyl-5-imidazolinone glycine</Name>
-<AlternateName>2-(3,4,5,6-tetrahydropyridin-2-yl)-1-carboxymethyl-1-imidazolin-5-one</AlternateName>
-<AlternateName>2-(tetrahydropyrid-2-yl)-5-imidazolinone glycine</AlternateName>
-<AlternateName>para-hydroxybenzylidene-imidazolidinone chromophore</AlternateName>
-<AlternateName>Zoanthus sp. fluorescent protein zFP538 chromophore</AlternateName>
-<AlternateName>[5-oxo-2-(3,4,5,6-tetrahydropyridin-2-yl)-4,5-dihydro-1H-imidazol-1-yl]acetic acid</AlternateName>
-<SystematicName>[5-oxo-2-(3,4,5,6-tetrahydropyridin-2-yl)-4,5-dihydro-1H-imidazol-1-yl]acetic acid</SystematicName>
-<Xref>PDBHET:CH7</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 8 H 9 N 2 O 1</Formula>
-<Weight type="chemical">149.17</Weight>
-<Weight type="physical">149.071488</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012 AA0008">
-<Formula>C 0 H -7 N -1 O -1</Formula>
-<Weight type="chemical">-37.06</Weight>
-<Weight type="physical">-37.052764</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Matz, M.V.</Author>
-<Author>Fradkov, A.F.</Author>
-<Author>Labas, Y.A.</Author>
-<Author>Savitsky, A.P.</Author>
-<Author>Zaraisky, A.G.</Author>
-<Author>Markelov, M.L.</Author>
-<Author>Lukyanov, S.A.</Author>
-</Authors>
-<Citation>Nature Biotechnol. 17, 969-973, 1999</Citation>
-<Title>Fluorescent proteins from nonbioluminescent Anthozoa species.</Title>
-<Xref>DOI:10.1038/13657</Xref>
-<Xref>PMID:10504696</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Remington, S.J.</Author>
-<Author>Wachter, R.M.</Author>
-<Author>Yarbrough, D.K.</Author>
-<Author>Branchaud, B.</Author>
-<Author>Anderson, D.C.</Author>
-<Author>Kallio, K.</Author>
-<Author>Lukyanov, K.A.</Author>
-</Authors>
-<Citation>Biochemistry 44, 202-212, 2005</Citation>
-<Title>zFP538, a yellow-fluorescent protein from Zoanthus, contains a novel three-ring chromophore.</Title>
-<Xref>DOI:10.1021/bi048383r</Xref>
-<Xref>PMID:15628861</Xref>
-<Note>X-ray diffraction, 2.70 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Remington, S.J.</Author>
-<Author>Wachter, R.M.</Author>
-<Author>Yarbrough, D.K.</Author>
-<Author>Branchaud, B.</Author>
-<Author>Anderson, D.C.</Author>
-<Author>Kallio, K.</Author>
-<Author>Lukyanov, K.A.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, August 2004</Citation>
-<Description>Crystal Structure of Wild Type Yellow Fluorescent Protein zFP538 from Zoanthus.</Description>
-<Xref>PDB:1XAE</Xref>
-<Note>X-ray diffraction, 2.70 angstroms</Note>
-</ReferenceBlock>
-<Comment>This entry represents the cross-link of the peptide backbone from the alpha-carboxyl carbon of residue N, a lysine, to the alpha-amino nitrogen of residue N+2, a glycine, coupled with the formation of a double bond to the alpha-amino nitrogen of residue N+1 which loses one hydrogen, and the loss of a molecule of water. In addition, the residue N lysine undergoes cyclization. The alpha-amino nitrogen is replaced by the epsilon-amino nitrogen, the peptide chain is broken, residue N-1 is released as an amide, and a double bond is formed between the alpha-carbon and the nitrogen so that a tetrahydropyridine ring results.</Comment>
-<Comment>This cross-link is accompanied by modification of residue N+1. The modified residue N+1 is presented in a separate entry and is not included in the mass accounting of this entry. The backbone atoms of residue N+1 are shown in gray in the diagram.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>G, K</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Condition>carboxamidine</Condition>
-<Condition>cross-link 1</Condition>
-<Condition>incidental to RESID:AA0183</Condition>
-<Condition>incidental to RESID:AA0365</Condition>
-<Xref>GO:0051362</Xref>
-<Xref>PSI-MOD:00387</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chromoprotein</Keyword>
-<Keyword>imidazolinone/oxazolinone ring</Keyword>
-<Keyword>pyridine ring</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__2-tetrahydro-2-pyridyl-5-imidazolinone (lys-gly)__k__g">CROSSLNK 2-tetrahydro-2-pyridyl-5-imidazolinone (Lys-Gly)</Feature>
-</Features>
-<Image src="/images/AA0382.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0382.PDB" />
-</Entry>
-<Entry id="AA0383">
-<Header>
-<Code>AA0383</Code>
-<Dates>
-<CreationDate>25-Feb-2005</CreationDate>
-<StrucRevDate>25-Feb-2005</StrucRevDate>
-<TextChngDate>30-Apr-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-alanyl-pentaglycyl-murein peptidoglycan</Name>
-<AlternateName>(2R,6S)-2-(N-mureinyl-(R)-alanyl-(S)-isoglutamyl)amino-6-(alanyl-pentaglycyl)amino-pimeloyl-(S)-alanyl-(S)-alanine</AlternateName>
-</Names>
-<FormulaBlock>
-<Formula>C 13 H 20 N 6 O 6 +</Formula>
-<Weight type="chemical">356.34 +</Weight>
-<Weight type="physical">356.144432 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0001">
-<Formula>C 10 H 14 N 5 O 4 +</Formula>
-<Weight type="chemical">268.25 +</Weight>
-<Weight type="physical">268.104579 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>de Chateau, M.</Author>
-<Author>Bjoerck, L.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 269, 12147-12151, 1994</Citation>
-<Title>Protein PAB, a mosaic albumin-binding bacterial protein representing the first contemporary example of module shuffling.</Title>
-<Xref>PMID:8163519</Xref>
-</ReferenceBlock>
-<Comment>This modification may be unique to the species Finegoldia magna (Peptostreptococcus magnus).</Comment>
-<GeneratingEnzyme>
-<EnzymeName>sortase aminoacyltransferase (EC 2.3.2.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>A</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>GO:0051363</Xref>
-<Xref>PSI-MOD:00388</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>glycoprotein</Keyword>
-<Keyword>peptidoglycan</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__pentaglycyl murein peptidoglycan amidated alanine__a">MOD_RES Pentaglycyl murein peptidoglycan amidated alanine</Feature>
-</Features>
-<Image src="/images/AA0383.GIF" alt="DUMMY.GIF" />
-</Entry>
-<Entry id="AA0384">
-<Header>
-<Code>AA0384</Code>
-<Dates>
-<CreationDate>25-Feb-2005</CreationDate>
-<StrucRevDate>25-Feb-2005</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-formyl-L-proline</Name>
-<AlternateName>1-formyl-2-pyrrolidinecarboxylic acid</AlternateName>
-<AlternateName>1-formylproline</AlternateName>
-<SystematicName>(2S)-1-formylpyrrolidine-2-carboxylic acid</SystematicName>
-<Xref>CAS:13200-83-4</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 8 N 1 O 2</Formula>
-<Weight type="chemical">126.14</Weight>
-<Weight type="physical">126.055504</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0015">
-<Formula>C 1 H 0 N 0 O 1</Formula>
-<Weight type="chemical">28.01</Weight>
-<Weight type="physical">27.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fujiki, H.</Author>
-<Author>Braunitzer, G.</Author>
-<Author>Rudloff, V.</Author>
-</Authors>
-<Citation>Hoppe-Seyler's Z. Physiol. Chem. 351, 901-902, 1970</Citation>
-<Title>N-Formylproline as N-terminal amino acid of lamprey haemoglobin.</Title>
-<Xref>DOI:10.1515/bchm2.1970.351.2.893</Xref>
-<Xref>PMID:5464655</Xref>
-<Note>this reported modification is probably artifactual; the publisher's DOI is incorrectly processed, the article can be accessed with the preceeding article beginning at page 893</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fuchigami, T.</Author>
-<Author>Misumi, S.</Author>
-<Author>Takamune, N.</Author>
-<Author>Takahashi, I.</Author>
-<Author>Takama, M.</Author>
-<Author>Shoji, S.</Author>
-</Authors>
-<Citation>Biochem. Biophys. Res. Commun. 293, 1107-1113, 2002</Citation>
-<Title>Acid-labile formylation of amino terminal proline of human immunodeficiency virus type 1 p24(gag) was found by proteomics using two-dimensional gel electrophoresis and matrix-assisted laser desorption/ionization-time-of-flight mass spectrometry.</Title>
-<Xref>DOI:10.1016/S0006-291X(02)00329-7</Xref>
-<Xref>PMID:12051774</Xref>
-<Note>it is not demonstrated that this modification is enzymatically produced</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gevaert, K.</Author>
-<Author>Goethals, M.</Author>
-<Author>Martens, L.</Author>
-<Author>Van Damme, J.</Author>
-<Author>Staes, A.</Author>
-<Author>Thomas, G.R.</Author>
-<Author>Vandekerckhove, J.</Author>
-</Authors>
-<Citation>Nature Biotechnol. 21, 566-569, 2003</Citation>
-<Title>Exploring proteomes and analyzing protein processing by mass spectrometric identification of sorted N-terminal peptides.</Title>
-<Xref>DOI:10.1038/nbt810</Xref>
-<Xref>PMID:12665801</Xref>
-<Note>the peptide proposed to have an N-formylproline was supposedly isolated from human tissue, but the sequence identified by mass analysis was the product of an engineered, artificial gene sequence; the identification has been acknowledged to be spurious (by private communication) and no alternative interpretation has been offered</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>P</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0051364</Xref>
-<Xref>PSI-MOD:00389</Xref>
-</SequenceCode>
-<Source>deprecated</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-<Keyword>formylation</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0384.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0384.PDB" />
-</Entry>
-<Entry id="AA0385">
-<Header>
-<Code>AA0385</Code>
-<Dates>
-<CreationDate>27-May-2005</CreationDate>
-<StrucRevDate>27-May-2005</StrucRevDate>
-<TextChngDate>25-Feb-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-decanoyl-L-serine</Name>
-<AlternateName>L-serine decanoate ester</AlternateName>
-<AlternateName>O3-decanoyl-L-serine</AlternateName>
-<SystematicName>(2S)-2-amino-3-(decanoyloxy)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 13 H 23 N 1 O 3</Formula>
-<Weight type="chemical">241.33</Weight>
-<Weight type="physical">241.167794</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 10 H 18 N 0 O 1</Formula>
-<Weight type="chemical">154.25</Weight>
-<Weight type="physical">154.135765</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kaiya, H.</Author>
-<Author>Kojima, M.</Author>
-<Author>Hosoda, H.</Author>
-<Author>Riley, L.G.</Author>
-<Author>Hirano, T.</Author>
-<Author>Grau, E.G.</Author>
-<Author>Kangawa, K.</Author>
-</Authors>
-<Citation>J. Endocrinol. 176, 415-423, 2003</Citation>
-<Title>Amidated fish ghrelin: purification, cDNA cloning in the Japanese eel and its biological activity.</Title>
-<Xref>DOI:10.1677/joe.0.1760415</Xref>
-<Xref>PMID:12630926</Xref>
-<Note>mass spectrometric identification</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>ghrelin O-acyltransferase, GOAT (EC 2.3.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>GO:0042050</Xref>
-<Xref>GO:0051367</Xref>
-<Xref>PSI-MOD:00390</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lipoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__o-decanoyl serine__s">LIPID O-decanoyl serine</Feature>
-</Features>
-<Image src="/images/AA0385.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0385.PDB" />
-</Entry>
-<Entry id="AA0386">
-<Header>
-<Code>AA0386</Code>
-<Dates>
-<CreationDate>27-May-2005</CreationDate>
-<StrucRevDate>27-May-2005</StrucRevDate>
-<TextChngDate>30-Sep-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-octanoyl-L-threonine</Name>
-<AlternateName>L-threonine octanoate ester</AlternateName>
-<AlternateName>O3-octanoyl-L-threonine</AlternateName>
-<SystematicName>(2S)-2-amino-3-(octanoyloxy)butanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 12 H 21 N 1 O 3</Formula>
-<Weight type="chemical">227.30</Weight>
-<Weight type="physical">227.152144</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0017">
-<Formula>C 8 H 14 N 0 O 1</Formula>
-<Weight type="chemical">126.20</Weight>
-<Weight type="physical">126.104465</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kaiya, H.</Author>
-<Author>Kojima, M.</Author>
-<Author>Hosoda, H.</Author>
-<Author>Koda, A.</Author>
-<Author>Yamamoto, K.</Author>
-<Author>Kitajima, Y.</Author>
-<Author>Matsumoto, M.</Author>
-<Author>Minamitake, Y.</Author>
-<Author>Kikuyama, S.</Author>
-<Author>Kangawa, K.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 276, 40441-40448, 2001</Citation>
-<Title>Bullfrog ghrelin is modified by n-octanoic acid at its third threonine residue.</Title>
-<Xref>DOI:10.1074/jbc.M105212200</Xref>
-<Xref>PMID:11546772</Xref>
-<Note>mass spectrometric identification</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>ghrelin O-acyltransferase, GOAT (EC 2.3.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>T</SequenceSpec>
-<Xref>GO:0042050</Xref>
-<Xref>GO:0051368</Xref>
-<Xref>PSI-MOD:00391</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lipoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__o-octanoyl threonine__t">LIPID O-octanoyl threonine</Feature>
-</Features>
-<Image src="/images/AA0386.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0386.PDB" />
-</Entry>
-<Entry id="AA0387">
-<Header>
-<Code>AA0387</Code>
-<Dates>
-<CreationDate>27-May-2005</CreationDate>
-<StrucRevDate>27-May-2005</StrucRevDate>
-<TextChngDate>25-Feb-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-decanoyl-L-threonine</Name>
-<AlternateName>L-threonine decanoate ester</AlternateName>
-<AlternateName>O3-decanoyl-L-threonine</AlternateName>
-<SystematicName>(2S)-2-amino-3-(decanoyloxy)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 14 H 25 N 1 O 3</Formula>
-<Weight type="chemical">255.36</Weight>
-<Weight type="physical">255.183444</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0017">
-<Formula>C 10 H 18 N 0 O 1</Formula>
-<Weight type="chemical">154.25</Weight>
-<Weight type="physical">154.135765</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kaiya, H.</Author>
-<Author>Kojima, M.</Author>
-<Author>Hosoda, H.</Author>
-<Author>Koda, A.</Author>
-<Author>Yamamoto, K.</Author>
-<Author>Kitajima, Y.</Author>
-<Author>Matsumoto, M.</Author>
-<Author>Minamitake, Y.</Author>
-<Author>Kikuyama, S.</Author>
-<Author>Kangawa, K.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 276, 40441-40448, 2001</Citation>
-<Title>Bullfrog ghrelin is modified by n-octanoic acid at its third threonine residue.</Title>
-<Xref>DOI:10.1074/jbc.M105212200</Xref>
-<Xref>PMID:11546772</Xref>
-<Note>mass spectrometric identification</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>ghrelin O-acyltransferase, GOAT (EC 2.3.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>T</SequenceSpec>
-<Xref>GO:0042050</Xref>
-<Xref>GO:0051369</Xref>
-<Xref>PSI-MOD:00392</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lipoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__o-decanoyl threonine__t">LIPID O-decanoyl threonine</Feature>
-</Features>
-<Image src="/images/AA0387.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0387.PDB" />
-</Entry>
-<Entry id="AA0388">
-<Header>
-<Code>AA0388</Code>
-<Dates>
-<CreationDate>28-Oct-2005</CreationDate>
-<StrucRevDate>28-Oct-2005</StrucRevDate>
-<TextChngDate>30-Sep-2008</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>4-hydroxy-D-valine</Name>
-<AlternateName>D-gamma-hydroxyvaline</AlternateName>
-<SystematicName>(2R,3Xi)-2-amino-4-hydroxy-3-methylbutanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 9 N 1 O 2</Formula>
-<Weight type="chemical">115.13</Weight>
-<Weight type="physical">115.063329</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0020">
-<Formula>C 0 H 0 N 0 O 1</Formula>
-<Weight type="chemical">16.00</Weight>
-<Weight type="physical">15.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Pisarewicz, K.</Author>
-<Author>Mora, D.</Author>
-<Author>Pflueger, F.C.</Author>
-<Author>Fields, G.B.</Author>
-<Author>Mari, F.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 127, 6207-6215, 2005</Citation>
-<Title>Polypeptide chains containing D-gamma-hydroxyvaline.</Title>
-<Xref>DOI:10.1021/ja050088m</Xref>
-<Xref>PMID:15853325</Xref>
-<Note>mass spectrographic, and 1D- and 2D-TOCSY NMR analysis; both the (2R,3R) and the (2R,3S) diastereomeric forms are apparently produced</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>V</SequenceSpec>
-<Condition>secondary to RESID:AA0200</Condition>
-<Xref>PSI-MOD:00756</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>D-amino acid</Keyword>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__d-4-hydroxyvaline__v">MOD_RES D-4-hydroxyvaline</Feature>
-</Features>
-<Image src="/images/AA0388.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0388.PDB" />
-</Entry>
-<Entry id="AA0389">
-<Header>
-<Code>AA0389</Code>
-<Dates>
-<CreationDate>28-Oct-2005</CreationDate>
-<StrucRevDate>28-Oct-2005</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O4-galactosyl-L-hydroxyproline</Name>
-<AlternateName>4-(beta-D-galactopyranosyloxy)proline</AlternateName>
-<AlternateName>4-(galactosyloxy)proline</AlternateName>
-<AlternateName>beta-galactopyranosyl-4-hydroxyproline</AlternateName>
-<AlternateName>O4-glycosyl-hydroxyproline</AlternateName>
-<SystematicName>(2S,4R)-4-(beta-D-galactopyranosyloxy)pyrrolidine-2-carboxylic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 11 H 17 N 1 O 7 +</Formula>
-<Weight type="chemical">275.26 +</Weight>
-<Weight type="physical">275.100502 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0015">
-<Formula>C 6 H 10 N 0 O 6 +</Formula>
-<Weight type="chemical">178.14 +</Weight>
-<Weight type="physical">178.047738 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fincher, G.B.</Author>
-<Author>Stone, B.A.</Author>
-</Authors>
-<Citation>Annu. Rev. Plant Physiol. 34, 47-70, 1983</Citation>
-<Title>Arabinogalactan-proteins: structure, biosynthesis, and function.</Title>
-<Xref>DOI:10.1146/annurev.pp.34.060183.000403</Xref>
-<Note>review</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Van den Bulck, K.</Author>
-<Author>Loosveld, A.M.A.</Author>
-<Author>Courtin, C.M.</Author>
-<Author>Proost, P.</Author>
-<Author>Van Damme, J.</Author>
-<Author>Robben, J.</Author>
-<Author>Mort, A.</Author>
-<Author>Delcour, J.A.</Author>
-</Authors>
-<Citation>Cereal Chem. 79, 329-331, 2002</Citation>
-<Title>Amino acid sequence of wheat flour arabinogalactan-peptide is identical to part of grain softness protein GSP-1, leads to an improved structural model.</Title>
-<Xref>DOI:10.1094/CCHEM.2002.79.3.329</Xref>
-</ReferenceBlock>
-<Comment>See also RESID:AA0212 and RESID:AA0390 for other O4-glycosylated 4-hydroxyprolines.</Comment>
-<SequenceCode>
-<SequenceSpec>P</SequenceSpec>
-<Condition>secondary to RESID:AA0030</Condition>
-<Xref>PSI-MOD:00757</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__o-linked (gal...) proline__p">CARBOHYD O-linked (Gal...) hydroxyproline</Feature>
-</Features>
-<Image src="/images/AA0389.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0389.PDB" />
-</Entry>
-<Entry id="AA0390">
-<Header>
-<Code>AA0390</Code>
-<Dates>
-<CreationDate>28-Oct-2005</CreationDate>
-<StrucRevDate>28-Oct-2005</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O4-(N-acetylamino)glucosyl-L-hydroxyproline</Name>
-<AlternateName>4-(N-acetylglucosaminyloxy)proline</AlternateName>
-<AlternateName>4-[(2-N-acetylamino)-alpha-D-glucopyranosyl]oxyproline</AlternateName>
-<AlternateName>alpha-2-(N-acetylamino)glucopyranosyl-4-hydroxyproline</AlternateName>
-<AlternateName>O4-glycosyl-hydroxyproline</AlternateName>
-<SystematicName>(2S,4R)-4-[2-acetamido-2-deoxy-alpha-D-glucopyranosyloxy]pyrrolidine-2-carboxylic acid</SystematicName>
-<Xref>CAS:10036-64-3</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 13 H 20 N 2 O 7 +</Formula>
-<Weight type="chemical">316.31 +</Weight>
-<Weight type="physical">316.127051 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0015">
-<Formula>C 8 H 13 N 1 O 6 +</Formula>
-<Weight type="chemical">219.19 +</Weight>
-<Weight type="physical">219.074287 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Teng-umnuay, P.</Author>
-<Author>Morris, H.R.</Author>
-<Author>Dell, A.</Author>
-<Author>Panico, M.</Author>
-<Author>Paxton, T.</Author>
-<Author>West, C.M.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 273, 18242-18249, 1998</Citation>
-<Title>The cytoplasmic F-box binding protein SKP1 contains a novel pentasaccharide linked to hydroxyproline in Dictyostelium.</Title>
-<Xref>DOI:10.1074/jbc.273.29.18242</Xref>
-<Xref>PMID:9660787</Xref>
-<Note>the polysaccharide structure is described with N-acetylglucosamine glycosylating hydroxyproline</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>West, C.M.</Author>
-<Author>Van Der Wel, H.</Author>
-<Author>Sassi, S.</Author>
-<Author>Gaucher, E.A.</Author>
-</Authors>
-<Citation>Biochim. Biophys. Acta 1673, 29-44, 2004</Citation>
-<Title>Cytoplasmic glycosylation of protein-hydroxyproline and its relationship to other glycosylation pathways.</Title>
-<Xref>DOI:10.1016/j.bbagen.2004.04.007</Xref>
-<Xref>PMID:15238247</Xref>
-<Note>the initial enzymatic reactions are described and the modification is identified as O4-alpha-(N-acetylamino)glucosyl-hydroxyproline</Note>
-</ReferenceBlock>
-<Comment>See also RESID:AA0212 and RESID:AA0389 for other O4-glycosylated 4-hydroxyprolines.</Comment>
-<SequenceCode>
-<SequenceSpec>P</SequenceSpec>
-<Condition>secondary to RESID:AA0030</Condition>
-<Xref>PSI-MOD:00758</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__o-linked (glcnac...) hydroxyproline__p">CARBOHYD O-linked (GlcNAc...) hydroxyproline</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="carbohyd__o-linked (hexnac...) hydroxyproline__p">CARBOHYD O-linked (HexNAc...) hydroxyproline</Feature>
-<Note>this UniProt feature is used when the identity of the sugar has not been determined</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0390.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0390.PDB" />
-</Entry>
-<Entry id="AA0391">
-<Header>
-<Code>AA0391</Code>
-<Dates>
-<CreationDate>02-Dec-2005</CreationDate>
-<StrucRevDate>02-Dec-2005</StrucRevDate>
-<TextChngDate>31-Dec-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>2-(S-L-cysteinyl)pyruvic acid O-phosphothioketal</Name>
-<AlternateName>2-([(2R)-2-amino-2-carboxyethyl]sulfanyl)-2-(phosphonooxy)propanoic acid</AlternateName>
-<AlternateName>2-([(2R)-2-azanyl-2-carboxyethyl]sulfanyl)-2-(phosphonooxy)propanoic acid</AlternateName>
-<AlternateName>cysteinyl pyruvate O-phosphothioketal</AlternateName>
-<AlternateName>phosphoenolpyruvate cysteine adduct</AlternateName>
-<AlternateName>phospholactoyl cysteine adduct</AlternateName>
-<AlternateName>S-[1-carboxy-1-(phosphonooxy)ethyl]cysteine</AlternateName>
-<SystematicName>(2R)-2-amino-3-[1-carboxy-1-(phosphonooxy)ethyl]sulfanylpropanoic acid</SystematicName>
-<Xref>PDBHET:QPA</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 10 N 1 O 7 P 1 S 1</Formula>
-<Weight type="chemical">271.18</Weight>
-<Weight type="physical">270.991559</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 3 H 5 N 0 O 6 P 1 S 0</Formula>
-<Weight type="chemical">168.04</Weight>
-<Weight type="physical">167.982375</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Cassidy, P.J.</Author>
-<Author>Kahan, F.M.</Author>
-</Authors>
-<Citation>Biochemistry 12, 1364-1374, 1973</Citation>
-<Title>A stable enzyme-phosphoenolpyruvate intermediate in the synthesis of uridine-5'-diphospho-N-acetyl-2-amino-2-deoxyglucose 3-O-enolpyruvyl ether.</Title>
-<Xref>DOI:10.1021/bi00731a017</Xref>
-<Xref>PMID:4696757</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ramilo, C.</Author>
-<Author>Appleyard, R.J.</Author>
-<Author>Wanke, C.</Author>
-<Author>Krekel, F.</Author>
-<Author>Amrhein, N.</Author>
-<Author>Evans, J.N.</Author>
-</Authors>
-<Citation>Biochemistry 33, 15071-15079, 1994</Citation>
-<Title>Detection of the covalent intermediate of UDP-N-acetylglucosamine enolpyruvyl transferase by solution-state and time-resolved solid-state NMR spectroscopy.</Title>
-<Xref>DOI:10.1021/bi00254a016</Xref>
-<Xref>PMID:7999765</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kim, D.H.</Author>
-<Author>Lees, W.J.</Author>
-<Author>Kempsell, K.E.</Author>
-<Author>Lane, W.S.</Author>
-<Author>Duncan, K.</Author>
-<Author>Walsh, C.T.</Author>
-</Authors>
-<Citation>Biochemistry 35, 4923-4928, 1996</Citation>
-<Title>Characterization of a Cys115 to Asp substitution in the Escherichia coli cell wall biosynthetic enzyme UDP-GlcNAc enolpyruvyl transferase (MurA) that confers resistance to inactivation by the antibiotic fosfomycin.</Title>
-<Xref>DOI:10.1021/bi952937w</Xref>
-<Xref>PMID:8664284</Xref>
-<Note>it is demonstrated that Cys-115 acts catalytically as a proton donor, but that formation of the covalent adduct with phosphoenolpyruvate is not required for catalysis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Zhu, J.Y.</Author>
-<Author>Yang, Y.</Author>
-<Author>Han, H.</Author>
-<Author>Betzi, S.</Author>
-<Author>Olesen, S.H.</Author>
-<Author>Marsilio, F.</Author>
-<Author>Schönbrunn, E.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 287, 12657-12667, 2012</Citation>
-<Title>Functional consequence of covalent reaction of phosphoenolpyruvate with UDP-N-acetylglucosamine 1-carboxyvinyltransferase (MurA).</Title>
-<Xref>DOI:10.1074/jbc.M112.342725</Xref>
-<Xref>PMID:22378791</Xref>
-<Note>X-ray diffraction, 1.81 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Zhu, J.Y.</Author>
-<Author>Schonbrunn, E.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, August 1996</Citation>
-<Description>Aquifex aeolicus MurA in complex with UDP-N-acetylmuramic acid and covalent adduct of PEP with Cys124.</Description>
-<Xref>PDB:3SWG</Xref>
-<Note>X-ray diffraction, 1.81 angstroms; an alternative model to PDB:2YVW</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>3-phosphoshikimate 1-carboxyvinyltransferase (EC 2.5.1.19)</EnzymeName>
-<EnzymeName>UDP-N-acetylglucosamine 1-carboxyvinyltransferase (EC 2.5.1.7)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>PSI-MOD:00797</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>phosphoprotein</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__2-(S-cysteinyl)pyruvic acid o-phosphothioketal__c">MOD_RES 2-(S-cysteinyl)pyruvic acid O-phosphothioketal</Feature>
-</Features>
-<Image src="/images/AA0391.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0391.PDB" />
-</Entry>
-<Entry id="AA0392">
-<Header>
-<Code>AA0392</Code>
-<Dates>
-<CreationDate>02-Dec-2005</CreationDate>
-<StrucRevDate>02-Dec-2005</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-galactosyl-L-cysteine</Name>
-<AlternateName>S-(beta-D-galactopyranosyl)cysteine</AlternateName>
-<AlternateName>S-glycosyl-cysteine</AlternateName>
-<SystematicName>(2R)-2-amino-3-(D-galactopyranosylsulfanyl)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 15 N 1 O 6 S 1 +</Formula>
-<Weight type="chemical">265.28 +</Weight>
-<Weight type="physical">265.062008 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 6 H 10 N 0 O 5 S 0 +</Formula>
-<Weight type="chemical">162.14 +</Weight>
-<Weight type="physical">162.052823 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lote, C.J.</Author>
-<Author>Weiss, J.B.</Author>
-</Authors>
-<Citation>FEBS Lett. 16, 81-85, 1971</Citation>
-<Title>Identification of digalactosylcysteine in a glycopeptide isolated from urine by a new preparative technique.</Title>
-<Xref>DOI:10.1016/0014-5793(71)80337-X</Xref>
-<Xref>PMID:11945907</Xref>
-<Note>chromatographic detection and chemical characterization; S-galactosylcysteine peptide; the peptide was not isolated or characterized in subsequent work, and the reported peptide sequence has not been found in the human proteome</Note>
-</ReferenceBlock>
-<Comment>The beta form is shown.</Comment>
-<Comment>See also RESID:AA0152 and RESID:AA0560 for other S-glycosylated cysteines.</Comment>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>PSI-MOD:00799</Xref>
-</SequenceCode>
-<Source>deprecated</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__s-linked (gal...) cysteine__c">CARBOHYD S-linked (Gal...) cysteine</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="carbohyd__s-linked (hex...) cysteine__c">CARBOHYD S-linked (Hex...) cysteine</Feature>
-<Note>this UniProt feature is used when the identity of the sugar has not been determined</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0392.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0392.PDB" />
-</Entry>
-<Entry id="AA0393">
-<Header>
-<Code>AA0393</Code>
-<Dates>
-<CreationDate>31-Dec-2005</CreationDate>
-<StrucRevDate>31-Dec-2011</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-cysteinyl-L-histidino-homocitryl vanadium heptairon nonasulfide carbide</Name>
-<AlternateName>nitrogenase iron-vanadium cofactor</AlternateName>
-</Names>
-<FormulaBlock>
-<Formula>C 17 Fe 7 H 18 N 4 O 9 S 10 V 1</Formula>
-<Weight type="chemical">1184.81</Weight>
-<Weight type="physical">1184.316610</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0009">
-<Formula>C 8 Fe 7 H 6 N 0 O 7 S 9 V 1</Formula>
-<Weight type="chemical">944.53</Weight>
-<Weight type="physical">944.248513</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Joerger, R.D.</Author>
-<Author>Loveless, T.M.</Author>
-<Author>Pau, R.N.</Author>
-<Author>Mitchenall, L.A.</Author>
-<Author>Simon, B.H.</Author>
-<Author>Bishop, P.E.</Author>
-</Authors>
-<Citation>J. Bacteriol. 172, 3400-3408, 1990</Citation>
-<Title>Nucleotide sequences and mutational analysis of the structural genes for nitrogenase 2 of Azotobacter vinelandii.</Title>
-<Xref>PMID:2345152</Xref>
-</ReferenceBlock>
-<Comment>The structure is presumed to be analagous to the molybendum-iron-sulfur cluster (see RESID:AA0141). Cysteine binds one iron of a 4Fe-3S cluster; the other three irons are connected by three mu(2)-sulfides and one mu(6)-carbon to three irons of a V-3Fe-3S cluster; the vanadium is further bound by the 2-oxide and 2-carboxylate of homocitrate (2-hydroxy-1,2,4-butanetricarboxylic acid) and the pros-N of histidine.</Comment>
-<SequenceCode>
-<SequenceSpec>C, H</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Condition>incidental to RESID:AA0300</Condition>
-<Xref>PSI-MOD:00800</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>iron-sulfur protein</Keyword>
-<Keyword>metalloprotein</Keyword>
-<Keyword>vanadium</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt" key="metal__vanadium-iron-sulfur (7fe-v-9s-x-homocitryl)__c">METAL Vanadium-iron-sulfur (7Fe-V-9S-X-homocitryl)</Feature>
-<Note>these UniProt features have not been revised</Note>
-</FeatureNote>
-<FeatureNote>
-<Feature type="UniProt" key="metal__vanadium-iron-sulfur (7fe-v-9s-x-homocitryl); via pros nitrogen__h">METAL Vanadium-iron-sulfur (7Fe-V-9S-X-homocitryl); via pros nitrogen</Feature>
-<Note>these UniProt features have not been revised</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0393.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0393.PDB" />
-</Entry>
-<Entry id="AA0394">
-<Header>
-<Code>AA0394</Code>
-<Dates>
-<CreationDate>31-Dec-2005</CreationDate>
-<StrucRevDate>31-Dec-2011</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-cysteinyl-L-histidino-homocitryl octairon nonasulfide carbide</Name>
-<AlternateName>nitrogenase iron-iron cofactor</AlternateName>
-</Names>
-<FormulaBlock>
-<Formula>C 17 Fe 8 H 18 N 4 O 9 S 10</Formula>
-<FormalCharge>2-</FormalCharge>
-<Weight type="chemical">1189.71</Weight>
-<Weight type="physical">1189.308685</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0009">
-<Formula>C 8 Fe 8 H 6 N 0 O 7 S 9</Formula>
-<FormalCharge>2-</FormalCharge>
-<Weight type="chemical">949.43</Weight>
-<Weight type="physical">949.240588</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Pau, R.N.</Author>
-<Author>Eldridge, M.E.</Author>
-<Author>Lowe, D.J.</Author>
-<Author>Mitchenall, L.A.</Author>
-<Author>Eady, R.R.</Author>
-</Authors>
-<Citation>Biochem. J. 293, 101-107, 1993</Citation>
-<Title>Molybdenum-independent nitrogenases of Azotobacter vinelandii: a functional species of alternative nitrogenase-3 isolated from a molybdenum-tolerant strain contains an iron-molybdenum cofactor.</Title>
-<Xref>PMID:8392330</Xref>
-</ReferenceBlock>
-<Comment>The structure is presumed to be analagous to the molybendum-iron-sulfur cluster (see RESID:AA0141). Cysteine binds one iron of a 4Fe-3S cluster; the other three irons are connected by three mu-sulfides and one mu(6)-carbon to three irons of a Mo-3Fe-3S cluster; the molybdenum is further bound by the 2-oxide and 2-carboxylate of homocitrate (2-hydroxy-1,2,4-butanetricarboxylic acid) and the pros-N of histidine.</Comment>
-<SequenceCode>
-<SequenceSpec>C, H</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Condition>incidental to RESID:AA0300</Condition>
-<Xref>PSI-MOD:00801</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>iron-sulfur protein</Keyword>
-<Keyword>metalloprotein</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt" key="metal__iron-sulfur (8fe-9s-x-homocitryl)__c">METAL Iron-sulfur (8Fe-9S-X-homocitryl)</Feature>
-<Note>these UniProt features have not been revised</Note>
-</FeatureNote>
-<FeatureNote>
-<Feature type="UniProt" key="metal__iron-sulfur (8fe-9s-x-homocitryl); via pros nitrogen__h">METAL Iron-sulfur (8Fe-9S-X-homocitryl); via pros nitrogen</Feature>
-<Note>these UniProt features have not been revised</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0394.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0394.PDB" />
-</Entry>
-<Entry id="AA0395">
-<Header>
-<Code>AA0395</Code>
-<Dates>
-<CreationDate>31-Mar-2006</CreationDate>
-<StrucRevDate>31-Mar-2006</StrucRevDate>
-<TextChngDate>31-Jul-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-histidino vanadium tetraoxide</Name>
-<AlternateName>(4-[(2S)-2-amino-2-carboxyethyl]-1H-imidazol-1-yl) (dihydroxy)dioxovanadium</AlternateName>
-<AlternateName>1'-vanadato-L-histidine</AlternateName>
-<AlternateName>bromoperoxidase vanadium cofactor</AlternateName>
-<AlternateName>chloroperoxidase vanadium cofactor</AlternateName>
-<AlternateName>haloperoxidase vanadium cofactor</AlternateName>
-<AlternateName>histidine-1-vanadate</AlternateName>
-<AlternateName>histidine-N(epsilon)-vanadate</AlternateName>
-<AlternateName>histidine-N1'-vanadate</AlternateName>
-<AlternateName>N(tau)-vanadatohistidine</AlternateName>
-<AlternateName>tele-vanadatohistidine</AlternateName>
-<SystematicName>dihydrogen (4-[(2S)-2-amino-2-carboxyethyl]-1H-imidazol-1-yl) (tetraoxido)vanadate</SystematicName>
-<Xref>CAS:14333-18-7</Xref>
-<Xref>COMe:BIM000195</Xref>
-<Xref>PDBHET:VO4</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 9 N 3 O 5 V 1</Formula>
-<Weight type="chemical">254.10</Weight>
-<Weight type="physical">253.998180</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0009">
-<Formula>C 0 H 2 N 0 O 4 V 1</Formula>
-<Weight type="chemical">116.95</Weight>
-<Weight type="physical">116.939268</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Messerschmidt, A.</Author>
-<Author>Wever, R.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 93, 392-396, 1996</Citation>
-<Title>X-ray structure of a vanadium-containing enzyme: chloroperoxidase from the fungus Curvularia inaequalis.</Title>
-<Xref>DOI:10.1073/pnas.93.1.392</Xref>
-<Xref>PMID:8552646</Xref>
-<Note>X-ray diffraction, 2.1 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Messerschmidt, A.</Author>
-<Author>Prade, L.</Author>
-<Author>Wever, R.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, April 2001</Citation>
-<Description>Crystal structure of native vanadium-containing chloroperoxidase from Curvularia inaequalis.</Description>
-<Xref>PDB:1IDQ</Xref>
-<Note>X-ray diffraction, 2.03 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Weyand, M.</Author>
-<Author>Hecht, H.</Author>
-<Author>Kiess, M.</Author>
-<Author>Liaud, M.</Author>
-<Author>Vilter, H.</Author>
-<Author>Schomburg, D.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 293, 595-611, 1999</Citation>
-<Title>X-ray structure determination of a vanadium-dependent haloperoxidase from Ascophyllum nodosum at 2.0 A resolution.</Title>
-<Xref>DOI:10.1006/jmbi.1999.3179</Xref>
-<Xref>PMID:10543953</Xref>
-<Note>X-ray diffraction, 2.0 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Weyand, M.</Author>
-<Author>Hecht, H.J.</Author>
-<Author>Kiess, M.</Author>
-<Author>Liaud, M.F.</Author>
-<Author>Vilter, H.</Author>
-<Author>Schomburg, D.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, June 1999</Citation>
-<Description>X-ray SIRAS structure determination of a vanadium-dependent haloperoxidase from Ascophyllum nodosum at 2.0 A resolution.</Description>
-<Xref>PDB:1QI9</Xref>
-<Note>X-ray diffraction, 2.05 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Raugei, S.</Author>
-<Author>Carloni, P.</Author>
-</Authors>
-<Citation>J. Phys. Chem. B 110, 3747-3758, 2006</Citation>
-<Title>Structure and function of vanadium haloperoxidase.</Title>
-<Xref>DOI:10.1021/jp054901b</Xref>
-<Xref>PMID:16494433</Xref>
-<Note>quantum and molecular mechanics model study of electon configuartion, protonation and enzyme mechanism</Note>
-</ReferenceBlock>
-<Comment>The resting state electron configuration and protonation probably corresponds to dihydrogen (tetraoxido)vanadate(6+).</Comment>
-<SequenceCode>
-<SequenceSpec>H</SequenceSpec>
-<Xref>PSI-MOD:00802</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>metalloprotein</Keyword>
-<Keyword>vanadium</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt" key="metal__vanadium__h">METAL Vanadium</Feature>
-<Note>this UniProt feature has a structural misrepresentation</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0395.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0395.PDB" />
-</Entry>
-<Entry id="AA0396">
-<Header>
-<Code>AA0396</Code>
-<Dates>
-<CreationDate>31-Mar-2006</CreationDate>
-<StrucRevDate>31-Mar-2006</StrucRevDate>
-<TextChngDate>31-Mar-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>3-(L-cystein-S-yl)-L-tyrosine</Name>
-<AlternateName>2-amino-3-(2-amino-2-carboxyethylthio)-3-(4-hydroxyphenyl)propanoic acid</AlternateName>
-<AlternateName>S-(tyros-3'-yl)cysteine</AlternateName>
-<SystematicName>(2S,3R)-2-amino-3-([(2R)-2-amino-2-carboxyethyl]sulfanyl)-3-(4-hydroxyphenyl)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 12 H 12 N 2 O 3 S 1</Formula>
-<Weight type="chemical">264.30</Weight>
-<Weight type="physical">264.056863</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0019">
-<Formula>C 0 H -2 N 0 O 0 S 0</Formula>
-<Weight type="chemical">-2.02</Weight>
-<Weight type="physical">-2.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Diaz, A.</Author>
-<Author>Horjales, E.</Author>
-<Author>Rudino-Pinera, E.</Author>
-<Author>Arreola, R.</Author>
-<Author>Hansberg, W.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 342, 971-985, 2004</Citation>
-<Title>Unusual Cys-Tyr covalent bond in a large catalase.</Title>
-<Xref>DOI:10.1016/j.jmb.2004.07.027</Xref>
-<Xref>PMID:15342250</Xref>
-<Note>X-ray diffraction, 1.75 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Diaz, A.</Author>
-<Author>Horjales, E.</Author>
-<Author>Rudio-Piera, E.</Author>
-<Author>Arreola, R.</Author>
-<Author>Hansberg, W.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, April 2004</Citation>
-<Description>Crystal structure of the catalase-1 from Neurospora crassa, native structure at 1.75A resolution.</Description>
-<Xref>PDB:1SY7</Xref>
-<Note>X-ray diffraction, 1.75 angstroms</Note>
-</ReferenceBlock>
-<Comment>This modification should not be confused with 3'-(S-L-cysteinyl)-L-tyrosine (see RESID:AA0113).</Comment>
-<SequenceCode>
-<SequenceSpec>C, Y</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:00803</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__3-(s-cysteinyl)-tyrosine (cys-tyr)__c__y">CROSSLNK 3-(S-cysteinyl)-tyrosine (Cys-Tyr)</Feature>
-</Features>
-<Image src="/images/AA0396.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0396.PDB" />
-</Entry>
-<Entry id="AA0397">
-<Header>
-<Code>AA0397</Code>
-<Dates>
-<CreationDate>31-Mar-2006</CreationDate>
-<StrucRevDate>31-Mar-2006</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-glucosyl-L-serine</Name>
-<AlternateName>O-glycosylserine</AlternateName>
-<AlternateName>O3-glucosylserine</AlternateName>
-<SystematicName>(2S)-2-amino-3-(beta-D-glucopyranosyloxy)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 15 N 1 O 7 +</Formula>
-<Weight type="chemical">249.22 +</Weight>
-<Weight type="physical">249.084852 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 6 H 10 N 0 O 5 +</Formula>
-<Weight type="chemical">162.14 +</Weight>
-<Weight type="physical">162.052823 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Nishimura, H.</Author>
-<Author>Kawabata, S.</Author>
-<Author>Kisiel, W.</Author>
-<Author>Hase, S.</Author>
-<Author>Ikenaka, T.</Author>
-<Author>Takao, T.</Author>
-<Author>Shimonishi, Y.</Author>
-<Author>Iwanaga, S.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 264, 20320-20325, 1989</Citation>
-<Title>Identification of a disaccharide (Xyl-Glc) and a trisaccharide (Xyl2-Glc) O-glycosidically linked to a serine residue in the first epidermal growth factor-like domain of human factors VII and IX and protein Z and bovine protein Z.</Title>
-<Xref>PMID:2511201</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hase, S.</Author>
-<Author>Nishimura, H.</Author>
-<Author>Kawabata, S.</Author>
-<Author>Iwanaga, S.</Author>
-<Author>Ikenaka, T.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 265, 1858-1861, 1990</Citation>
-<Title>The structure of (xylose)2glucose-O-serine 53 found in the first epidermal growth factor-like domain of bovine blood clotting factor IX.</Title>
-<Xref>PMID:2105311</Xref>
-<Note>structural analysis; this modification has a beta-glycosidic linkage</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Moloney, D.J.</Author>
-<Author>Shair, L.H.</Author>
-<Author>Lu, F.M.</Author>
-<Author>Xia, J.</Author>
-<Author>Locke, R.</Author>
-<Author>Matta, K.L.</Author>
-<Author>Haltiwanger, R.S.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 275, 9604-9611, 2000</Citation>
-<Title>Mammalian Notch1 is modified with two unusual forms of O-linked glycosylation found on epidermal growth factor-like modules.</Title>
-<Xref>DOI:10.1074/jbc.275.13.9604</Xref>
-<Xref>PMID:10734111</Xref>
-</ReferenceBlock>
-<Comment>See also RESID:AA0154, RESID:AA0208, RESID:AA0209, RESID:AA0210, RESID:AA0291, RESID:AA0296, RESID:AA0297, RESID:AA0397, RESID:AA0398, RESID:AA0400, RESID:AA0402, RESID:AA0404, RESID:AA0406, and RESID:AA0422 for other O-glycosylated serines.</Comment>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>PSI-MOD:00804</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__o-linked (glc) serine__s">CARBOHYD O-linked (Glc) serine</Feature>
-<Feature type="UniProt" key="carbohyd__o-linked (glc...) serine__s">CARBOHYD O-linked (Glc...) serine</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="carbohyd__o-linked (hex) serine__s">CARBOHYD O-linked (Hex) serine</Feature>
-<Note>this UniProt feature is used when the identity of the sugar has not been determined</Note>
-</FeatureNote>
-<FeatureNote>
-<Feature type="UniProt" key="carbohyd__o-linked (hex...) serine__s">CARBOHYD O-linked (Hex...) serine</Feature>
-<Note>this UniProt feature is used when the identity of the sugar has not been determined</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0397.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0397.PDB" />
-</Entry>
-<Entry id="AA0398">
-<Header>
-<Code>AA0398</Code>
-<Dates>
-<CreationDate>31-Mar-2006</CreationDate>
-<StrucRevDate>31-Mar-2006</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-(N-acetylamino)glucosyl-L-serine</Name>
-<AlternateName>O-(2-acetylamino-2-deoxy-beta-D-glucopyranosyl)-L-serine</AlternateName>
-<AlternateName>O-(N-acetylglucosaminyl)serine</AlternateName>
-<AlternateName>O-glycosylserine</AlternateName>
-<AlternateName>O-seryl-beta-N-acetylglucosaminide</AlternateName>
-<AlternateName>O3-(2-acetamido-2-deoxy-beta-D-glucopyranosyl)-L-serine</AlternateName>
-<AlternateName>O3-(N-acetylglucosaminyl)serine</AlternateName>
-<SystematicName>(2S)-2-amino-3-(2-acetamido-2-deoxy-beta-D-glucopyranosyloxy)propanoic acid</SystematicName>
-<Xref>CAS:17041-36-0</Xref>
-<Xref>ChEBI:90838</Xref>
-<Xref>PDBHET:NAG</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 11 H 18 N 2 O 7 +</Formula>
-<Weight type="chemical">290.27 +</Weight>
-<Weight type="physical">290.111401 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 8 H 13 N 1 O 5 +</Formula>
-<Weight type="chemical">203.19 +</Weight>
-<Weight type="physical">203.079373 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Torres, C.R.</Author>
-<Author>Hart, G.W.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 259, 3308-3317, 1984</Citation>
-<Title>Topography and polypeptide distribution of terminal N-acetylglucosamine residues on the surfaces of intact lymphocytes. Evidence for O-linked GlcNAc.</Title>
-<Xref>PMID:6421821</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>D'Onofrio, M.</Author>
-<Author>Starr, C.M.</Author>
-<Author>Park, M.K.</Author>
-<Author>Holt, G.D.</Author>
-<Author>Haltiwanger, R.S.</Author>
-<Author>Hart, G.W.</Author>
-<Author>Hanover, J.A.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 85, 9595-9599, 1988</Citation>
-<Title>Partial cDNA sequence encoding a nuclear pore protein modified by O-linked N-acetylglucosamine.</Title>
-<Xref>DOI:10.1073/pnas.85.24.9595</Xref>
-<Xref>PMID:3200844</Xref>
-<Note>enzymatic radiolabeling and sequencing evidence for intracellular O-GlcNAc glycosylation of serine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Haynes, P.A.</Author>
-<Author>Gooley, A.A.</Author>
-<Author>Ferguson, M.A.</Author>
-<Author>Redmond, J.W.</Author>
-<Author>Williams, K.L.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 216, 729-737, 1993</Citation>
-<Title>Post-translational modifications of the Dictyostelium discoideum glycoprotein PsA. Glycosylphosphatidylinositol membrane anchor and composition of O-linked oligosaccharides.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1993.tb18192.x</Xref>
-<Xref>PMID:8404891</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Butkinaree, C.</Author>
-<Author>Park, K.</Author>
-<Author>Hart, G.W.</Author>
-</Authors>
-<Citation>Biochim. Biophys. Acta 1800, 96-106, 2010</Citation>
-<Title>O-linked beta-N-acetylglucosamine (O-GlcNAc): Extensive crosstalk with phosphorylation to regulate signaling and transcription in response to nutrients and stress.</Title>
-<Xref>DOI:10.1016/j.bbagen.2009.07.018</Xref>
-<Xref>PMID:19647786</Xref>
-<Note>review of regulatory GlcNAc O-glycosylation</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lazarus, M.B.</Author>
-<Author>Nam, Y.</Author>
-<Author>Jiang, J.</Author>
-<Author>Sliz, P.</Author>
-<Author>Walker, S.</Author>
-</Authors>
-<Citation>Nature 469, 564-567, 2011</Citation>
-<Title>Structure of human O-GlcNAc transferase and its complex with a peptide substrate.</Title>
-<Xref>DOI:10.1038/nature09638</Xref>
-<Xref>PMID:21240259</Xref>
-<Note>X-ray diffraction of generating enzyme with substrate, at 1.95 and 2.78 angstroms</Note>
-</ReferenceBlock>
-<Comment>See also RESID:AA0154, RESID:AA0208, RESID:AA0209, RESID:AA0210, RESID:AA0291, RESID:AA0296, RESID:AA0297, RESID:AA0397, RESID:AA0400, RESID:AA0402, RESID:AA0404, RESID:AA0406, and RESID:AA0422 for other O-glycosylated serines.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>protein O-GlcNAc transferase (EC 2.4.1.255)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>PSI-MOD:00805</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__o-linked (glcnac) serine__s">CARBOHYD O-linked (GlcNAc) serine</Feature>
-<Feature type="UniProt" key="carbohyd__o-linked (glcnac...) serine__s">CARBOHYD O-linked (GlcNAc...) serine</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="carbohyd__o-linked (hexnac) serine__s">CARBOHYD O-linked (HexNAc) serine</Feature>
-<Note>this UniProt feature is used when the identity of the sugar has not been determined</Note>
-</FeatureNote>
-<FeatureNote>
-<Feature type="UniProt" key="carbohyd__o-linked (hexnac...) serine__s">CARBOHYD O-linked (HexNAc...) serine</Feature>
-<Note>this UniProt feature is used when the identity of the sugar has not been determined</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0398.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0398.PDB" />
-</Entry>
-<Entry id="AA0399">
-<Header>
-<Code>AA0399</Code>
-<Dates>
-<CreationDate>31-Mar-2006</CreationDate>
-<StrucRevDate>31-Mar-2006</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-(N-acetylamino)glucosyl-L-threonine</Name>
-<AlternateName>O-(2-acetylamino-2-deoxy-beta-D-glucopyranosyl)-L-threonine</AlternateName>
-<AlternateName>O-(N-acetylglucosaminyl)-L-threonine</AlternateName>
-<AlternateName>O-glycosylthreonine</AlternateName>
-<AlternateName>O-threonyl-beta-N-acetylglucosaminide</AlternateName>
-<AlternateName>O3-(2-acetamido-2-deoxy-beta-D-glucopyranosyl)-L-threonine</AlternateName>
-<AlternateName>O3-(N-acetylglucosaminyl)threonine</AlternateName>
-<SystematicName>(2S,3R)-2-amino-3-(2-acetamido-2-deoxy-beta-D-glucopyranosyloxy)butanoic acid</SystematicName>
-<Xref>ChEBI:90840</Xref>
-<Xref>PDBHET:NDG</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 12 H 20 N 2 O 7 +</Formula>
-<Weight type="chemical">304.30 +</Weight>
-<Weight type="physical">304.127051 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0017">
-<Formula>C 8 H 13 N 1 O 5 +</Formula>
-<Weight type="chemical">203.19 +</Weight>
-<Weight type="physical">203.079373 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Torres, C.R.</Author>
-<Author>Hart, G.W.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 259, 3308-3317, 1984</Citation>
-<Title>Topography and polypeptide distribution of terminal N-acetylglucosamine residues on the surfaces of intact lymphocytes. Evidence for O-linked GlcNAc.</Title>
-<Xref>PMID:6421821</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Haynes, P.A.</Author>
-<Author>Gooley, A.A.</Author>
-<Author>Ferguson, M.A.</Author>
-<Author>Redmond, J.W.</Author>
-<Author>Williams, K.L.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 216, 729-737, 1993</Citation>
-<Title>Post-translational modifications of the Dictyostelium discoideum glycoprotein PsA. Glycosylphosphatidylinositol membrane anchor and composition of O-linked oligosaccharides.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1993.tb18192.x</Xref>
-<Xref>PMID:8404891</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Butkinaree, C.</Author>
-<Author>Park, K.</Author>
-<Author>Hart, G.W.</Author>
-</Authors>
-<Citation>Biochim. Biophys. Acta 1800, 96-106, 2010</Citation>
-<Title>O-linked beta-N-acetylglucosamine (O-GlcNAc): Extensive crosstalk with phosphorylation to regulate signaling and transcription in response to nutrients and stress.</Title>
-<Xref>DOI:10.1016/j.bbagen.2009.07.018</Xref>
-<Xref>PMID:19647786</Xref>
-<Note>review of regulatory GlcNAc O-glycosylation</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lazarus, M.B.</Author>
-<Author>Nam, Y.</Author>
-<Author>Jiang, J.</Author>
-<Author>Sliz, P.</Author>
-<Author>Walker, S.</Author>
-</Authors>
-<Citation>Nature 469, 564-567, 2011</Citation>
-<Title>Structure of human O-GlcNAc transferase and its complex with a peptide substrate.</Title>
-<Xref>DOI:10.1038/nature09638</Xref>
-<Xref>PMID:21240259</Xref>
-<Note>X-ray diffraction of generating enzyme with substrate, at 1.95 and 2.78 angstroms</Note>
-</ReferenceBlock>
-<Comment>See also RESID:AA0155, RESID:AA0247, RESID:AA0401, RESID:AA0403, RESID:AA0405, and RESID:AA0515 for other O-glycosylated threonines.</Comment>
-<Comment>The PDB has some entries with threonine apparently alpha-glycosylated with N-acetylglucosamine. These are low resolution structures and appear to be erroneous.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>protein O-GlcNAc transferase (EC 2.4.1.255)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>T</SequenceSpec>
-<Xref>PSI-MOD:00806</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__o-linked (glcnac) threonine__t">CARBOHYD O-linked (GlcNAc) threonine</Feature>
-<Feature type="UniProt" key="carbohyd__o-linked (glcnac...) threonine__t">CARBOHYD O-linked (GlcNAc...) threonine</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="carbohyd__o-linked (hexnac) threonine__t">CARBOHYD O-linked (HexNAc) threonine</Feature>
-<Note>this UniProt feature is used when the identity of the sugar has not been determined</Note>
-</FeatureNote>
-<FeatureNote>
-<Feature type="UniProt" key="carbohyd__o-linked (hexnac...) threonine__t">CARBOHYD O-linked (HexNAc...) threonine</Feature>
-<Note>this UniProt feature is used when the identity of the sugar has not been determined</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0399.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0399.PDB" />
-</Entry>
-<Entry id="AA0400">
-<Header>
-<Code>AA0400</Code>
-<Dates>
-<CreationDate>31-Mar-2006</CreationDate>
-<StrucRevDate>31-Mar-2006</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-galactosyl-L-serine</Name>
-<AlternateName>O-glycosylserine</AlternateName>
-<AlternateName>O3-galactosylserine</AlternateName>
-<SystematicName>(2S)-2-amino-3-(alpha-D-galactopyranosyloxy)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 15 N 1 O 7</Formula>
-<Weight type="chemical">249.22</Weight>
-<Weight type="physical">249.084852</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 6 H 10 N 0 O 5</Formula>
-<Weight type="chemical">162.14</Weight>
-<Weight type="physical">162.052823</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Allen, A.K.</Author>
-<Author>Desai, N.N.</Author>
-<Author>Neuberger, A.</Author>
-<Author>Creeth, J.M.</Author>
-</Authors>
-<Citation>Biochem. J. 171, 665-674, 1978</Citation>
-<Title>Properties of potato lectin and the nature of its glycoprotein linkages.</Title>
-<Xref>PMID:666730</Xref>
-<Note>the modification is identified as O3-(alpha-galactosyl)-serine</Note>
-</ReferenceBlock>
-<Comment>See also RESID:AA0154, RESID:AA0208, RESID:AA0209, RESID:AA0210, RESID:AA0291, RESID:AA0296, RESID:AA0297, RESID:AA0397, RESID:AA0398, RESID:AA0402, RESID:AA0404, RESID:AA0406, and RESID:AA0422 for other O-glycosylated serines.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>galactosyltransferase (EC 2.4.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>PSI-MOD:00808</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__o-linked (gal) serine__s">CARBOHYD O-linked (Gal) serine</Feature>
-<Feature type="UniProt" key="carbohyd__o-linked (gal...) serine__s">CARBOHYD O-linked (Gal...) serine</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="carbohyd__o-linked (hex) serine__s">CARBOHYD O-linked (Hex) serine</Feature>
-<Note>this UniProt feature is used when the identity of the sugar has not been determined</Note>
-</FeatureNote>
-<FeatureNote>
-<Feature type="UniProt" key="carbohyd__o-linked (hex...) serine__s">CARBOHYD O-linked (Hex...) serine</Feature>
-<Note>this UniProt feature is used when the identity of the sugar has not been determined</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0400.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0400.PDB" />
-</Entry>
-<Entry id="AA0401">
-<Header>
-<Code>AA0401</Code>
-<Dates>
-<CreationDate>31-Mar-2006</CreationDate>
-<StrucRevDate>31-Mar-2006</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-galactosyl-L-threonine</Name>
-<AlternateName>O-glycosylthreonine</AlternateName>
-<AlternateName>O3-galactosylthreonine</AlternateName>
-<SystematicName>(2S,3R)-2-amino-3-(alpha-D-galactopyranosyloxy)butanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 10 H 17 N 1 O 7 +</Formula>
-<Weight type="chemical">263.25 +</Weight>
-<Weight type="physical">263.100502 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0017">
-<Formula>C 6 H 10 N 0 O 5 +</Formula>
-<Weight type="chemical">162.14 +</Weight>
-<Weight type="physical">162.052823 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lechner, J.</Author>
-<Author>Wieland, F.</Author>
-</Authors>
-<Citation>Annu. Rev. Biochem. 58, 173-194, 1989</Citation>
-<Title>Structure and biosynthesis of prokaryotic glycoproteins.</Title>
-<Xref>DOI:10.1146/annurev.bi.58.070189.001133</Xref>
-<Xref>PMID:2673008</Xref>
-</ReferenceBlock>
-<Comment>See also RESID:AA0155, RESID:AA0247, RESID:AA0399, RESID:AA0403, RESID:AA0405, and RESID:AA0515 for other O-glycosylated threonines.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>galactosyltransferase (EC 2.4.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>T</SequenceSpec>
-<Xref>PSI-MOD:00809</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__o-linked (gal) threonine__t">CARBOHYD O-linked (Gal) threonine</Feature>
-<Feature type="UniProt" key="carbohyd__o-linked (gal...) threonine__t">CARBOHYD O-linked (Gal...) threonine</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="carbohyd__o-linked (hex) threonine__t">CARBOHYD O-linked (Hex) threonine</Feature>
-<Note>this UniProt feature is used when the identity of the sugar has not been determined</Note>
-</FeatureNote>
-<FeatureNote>
-<Feature type="UniProt" key="carbohyd__o-linked (hex...) threonine__t">CARBOHYD O-linked (Hex...) threonine</Feature>
-<Note>this UniProt feature is used when the identity of the sugar has not been determined</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0401.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0401.PDB" />
-</Entry>
-<Entry id="AA0402">
-<Header>
-<Code>AA0402</Code>
-<Dates>
-<CreationDate>31-Mar-2006</CreationDate>
-<StrucRevDate>31-Mar-2006</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-mannosyl-L-serine</Name>
-<AlternateName>O-glycosylserine</AlternateName>
-<AlternateName>O-mannopyranosylserine</AlternateName>
-<AlternateName>O3-mannosylserine</AlternateName>
-<SystematicName>(2S)-2-amino-3-(alpha-D-mannopyranosyloxy)propanoic acid</SystematicName>
-<Xref>CAS:78609-14-0</Xref>
-<Xref>ChEBI:137321</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 15 N 1 O 7 +</Formula>
-<Weight type="chemical">249.22 +</Weight>
-<Weight type="physical">249.084852 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 6 H 10 N 0 O 5 +</Formula>
-<Weight type="chemical">162.14 +</Weight>
-<Weight type="physical">162.052823 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bause, E.</Author>
-<Author>Lehle, L.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 101, 531-540, 1979</Citation>
-<Title>Enzymatic N-glycosylation and O-glycosylation of synthetic peptide acceptors by dolichol-linked sugar derivatives in yeast.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1979.00531.pp.x</Xref>
-<Xref>PMID:391559</Xref>
-<Note>the enzyme was shown to produce alpha anomeric glycosides</Note>
-</ReferenceBlock>
-<Comment>See also RESID:AA0154, RESID:AA0208, RESID:AA0209, RESID:AA0210, RESID:AA0291, RESID:AA0296, RESID:AA0297, RESID:AA0397, RESID:AA0398, RESID:AA0400, RESID:AA0404, RESID:AA0406, and RESID:AA0422 for other O-glycosylated serines.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>dolichyl-phosphate-mannose-protein mannosyltransferase (EC 2.4.1.109)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>PSI-MOD:00810</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__o-linked (man) serine__s">CARBOHYD O-linked (Man) serine</Feature>
-<Feature type="UniProt" key="carbohyd__o-linked (man...) serine__s">CARBOHYD O-linked (Man...) serine</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="carbohyd__o-linked (hex) serine__s">CARBOHYD O-linked (Hex) serine</Feature>
-<Note>this UniProt feature is used when the identity of the sugar has not been determined</Note>
-</FeatureNote>
-<FeatureNote>
-<Feature type="UniProt" key="carbohyd__o-linked (hex...) serine__s">CARBOHYD O-linked (Hex...) serine</Feature>
-<Note>this UniProt feature is used when the identity of the sugar has not been determined</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0402.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0402.PDB" />
-</Entry>
-<Entry id="AA0403">
-<Header>
-<Code>AA0403</Code>
-<Dates>
-<CreationDate>31-Mar-2006</CreationDate>
-<StrucRevDate>31-Mar-2006</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-mannosyl-L-threonine</Name>
-<AlternateName>O-glycosylthreonine</AlternateName>
-<AlternateName>O3-mannosylthreonine</AlternateName>
-<SystematicName>(2S,3R)-2-amino-3-(alpha-D-mannopyranosyloxy)butanoic acid</SystematicName>
-<Xref>ChEBI:137323</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 10 H 17 N 1 O 7 +</Formula>
-<Weight type="chemical">263.25 +</Weight>
-<Weight type="physical">263.100502 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0017">
-<Formula>C 6 H 10 N 0 O 5 +</Formula>
-<Weight type="chemical">162.14 +</Weight>
-<Weight type="physical">162.052823 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bause, E.</Author>
-<Author>Lehle, L.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 101, 531-540, 1979</Citation>
-<Title>Enzymatic N-glycosylation and O-glycosylation of synthetic peptide acceptors by dolichol-linked sugar derivatives in yeast.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1979.00531.pp.x</Xref>
-<Xref>PMID:391559</Xref>
-<Note>the enzyme was shown to produce alpha anomeric glycosides</Note>
-</ReferenceBlock>
-<Comment>See also RESID:AA0155, RESID:AA0247, RESID:AA0399, RESID:AA0401, RESID:AA0405, and RESID:AA0515 for other O-glycosylated threonines.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>dolichyl-phosphate-mannose-protein mannosyltransferase (EC 2.4.1.109)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>T</SequenceSpec>
-<Xref>PSI-MOD:00811</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__o-linked (man) threonine__t">CARBOHYD O-linked (Man) threonine</Feature>
-<Feature type="UniProt" key="carbohyd__o-linked (man...) threonine__t">CARBOHYD O-linked (Man...) threonine</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="carbohyd__o-linked (hex) threonine__t">CARBOHYD O-linked (Hex) threonine</Feature>
-<Note>this UniProt feature is used when the identity of the sugar has not been determined</Note>
-</FeatureNote>
-<FeatureNote>
-<Feature type="UniProt" key="carbohyd__o-linked (hex...) threonine__t">CARBOHYD O-linked (Hex...) threonine</Feature>
-<Note>this UniProt feature is used when the identity of the sugar has not been determined</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0403.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0403.PDB" />
-</Entry>
-<Entry id="AA0404">
-<Header>
-<Code>AA0404</Code>
-<Dates>
-<CreationDate>31-Mar-2006</CreationDate>
-<StrucRevDate>31-Mar-2006</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-fucosyl-L-serine</Name>
-<AlternateName>O-glycosylserine</AlternateName>
-<AlternateName>O3-fucosylserine</AlternateName>
-<SystematicName>(2S)-2-amino-3-(6-deoxy-alpha-D-galactopyranosyloxy)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 15 N 1 O 6 +</Formula>
-<Weight type="chemical">233.22 +</Weight>
-<Weight type="physical">233.089937 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 6 H 10 N 0 O 4 +</Formula>
-<Weight type="chemical">146.14 +</Weight>
-<Weight type="physical">146.057909 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bjoern, S.</Author>
-<Author>Foster, D.C.</Author>
-<Author>Thim, L.</Author>
-<Author>Wiberg, F.C.</Author>
-<Author>Christensen, M.</Author>
-<Author>Komiyama, Y.</Author>
-<Author>Pedersen, A.H.</Author>
-<Author>Kisiel, W.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 266, 11051-11057, 1991</Citation>
-<Title>Human plasma and recombinant factor VII. Characterization of O-glycosylations at serine residues 52 and 60 and effects of site-directed mutagenesis of serine 52 to alanine.</Title>
-<Xref>PMID:1904059</Xref>
-<Note>detection by carbohydrate analysis; location by radioisotope labeling; characterized as a single fucose glycosylation</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Nishimura, H.</Author>
-<Author>Takao, T.</Author>
-<Author>Hase, S.</Author>
-<Author>Shimonishi, Y.</Author>
-<Author>Iwanaga, S.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 267, 17520-17525, 1992</Citation>
-<Title>Human factor IX has a tetrasaccharide O-glycosidically linked to serine 61 through the fucose residue.</Title>
-<Xref>PMID:1517205</Xref>
-<Note>detection by carbohydrate analysis; characterized as a tetrasaccharide glycosylation</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Moloney, D.J.</Author>
-<Author>Shair, L.H.</Author>
-<Author>Lu, F.M.</Author>
-<Author>Xia, J.</Author>
-<Author>Locke, R.</Author>
-<Author>Matta, K.L.</Author>
-<Author>Haltiwanger, R.S.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 275, 9604-9611, 2000</Citation>
-<Title>Mammalian Notch1 is modified with two unusual forms of O-linked glycosylation found on epidermal growth factor-like modules.</Title>
-<Xref>DOI:10.1074/jbc.275.13.9604</Xref>
-<Xref>PMID:10734111</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hofsteenge, J.</Author>
-<Author>Huwiler, K.G.</Author>
-<Author>Macek, B.</Author>
-<Author>Hess, D.</Author>
-<Author>Lawler, J.</Author>
-<Author>Mosher, D.F.</Author>
-<Author>Peter-Katalinic, J.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 276, 6485-6498, 2001</Citation>
-<Title>C-mannosylation and O-fucosylation of the thrombospondin type 1 module.</Title>
-<Xref>DOI:10.1074/jbc.M008073200</Xref>
-<Xref>PMID:11067851</Xref>
-<Note>mass spectrographic and linkage analysis; characterized as a tetrasaccharide glycosylation</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gonzalez de Peredo, A.</Author>
-<Author>Klein, D.</Author>
-<Author>Macek, B.</Author>
-<Author>Hess, D.</Author>
-<Author>Peter-Katalinic, J.</Author>
-<Author>Hofsteenge, J.</Author>
-</Authors>
-<Citation>Mol. Cell. Proteomics 1, 11-18, 2002</Citation>
-<Title>C-mannosylation and o-fucosylation of thrombospondin type 1 repeats.</Title>
-<Xref>DOI:10.1074/mcp.M100011-MCP200</Xref>
-<Xref>PMID:12096136</Xref>
-</ReferenceBlock>
-<Comment>See also RESID:AA0154, RESID:AA0208, RESID:AA0209, RESID:AA0210, RESID:AA0291, RESID:AA0296, RESID:AA0297, RESID:AA0397, RESID:AA0398, RESID:AA0400, RESID:AA0402, RESID:AA0406, and RESID:AA0422 for other O-glycosylated serines.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptide-O-fucosyltransferase (EC 2.4.1.221)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>PSI-MOD:00812</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__o-linked (fuc) serine__s">CARBOHYD O-linked (Fuc) serine</Feature>
-<Feature type="UniProt" key="carbohyd__o-linked (fuc...) serine__s">CARBOHYD O-linked (Fuc...) serine</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="carbohyd__o-linked (dhex) serine__t">CARBOHYD O-linked (dHex) serine</Feature>
-<Note>this UniProt feature is used when the identity of the sugar has not been determined</Note>
-</FeatureNote>
-<FeatureNote>
-<Feature type="UniProt" key="carbohyd__o-linked (dhex...) serine__t">CARBOHYD O-linked (dHex...) serine</Feature>
-<Note>this UniProt feature is used when the identity of the sugar has not been determined</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0404.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0404.PDB" />
-</Entry>
-<Entry id="AA0405">
-<Header>
-<Code>AA0405</Code>
-<Dates>
-<CreationDate>31-Mar-2006</CreationDate>
-<StrucRevDate>31-Mar-2006</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-fucosyl-L-threonine</Name>
-<AlternateName>O-glycosylthreonine</AlternateName>
-<AlternateName>O3-fucosylthreonine</AlternateName>
-<SystematicName>(2S,3R)-2-amino-3-(6-deoxy-alpha-D-galactopyranosyloxy)butanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 10 H 17 N 1 O 6 +</Formula>
-<Weight type="chemical">247.25 +</Weight>
-<Weight type="physical">247.105587 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0017">
-<Formula>C 6 H 10 N 0 O 4 +</Formula>
-<Weight type="chemical">146.14 +</Weight>
-<Weight type="physical">146.057909 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Harris, R.J.</Author>
-<Author>Leonard, C.K.</Author>
-<Author>Guzzetta, A.W.</Author>
-<Author>Spellman, M.W.</Author>
-</Authors>
-<Citation>Biochemistry 30, 2311-2314, 1991</Citation>
-<Title>Tissue plasminogen activator has an O-linked fucose attached to threonine-61 in the epidermal growth factor domain.</Title>
-<Xref>DOI:10.1021/bi00223a004</Xref>
-<Xref>PMID:1900431</Xref>
-<Note>this modification has an alpha-glycosidic linkage</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Nakakura, N.</Author>
-<Author>Hietter, H.</Author>
-<Author>Van Dorsselaer, A.</Author>
-<Author>Luu, B.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 204, 147-153, 1992</Citation>
-<Title>Isolation and structural determination of three peptides from the insect Locusta migratoria. Identification of a deoxyhexose-linked peptide.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1992.tb16617.x</Xref>
-<Xref>PMID:1740125</Xref>
-<Note>chromatographic and mass spectrometric identification of fucosyl threonine</Note>
-</ReferenceBlock>
-<Comment>See also RESID:AA0155, RESID:AA0247, RESID:AA0399, RESID:AA0401, RESID:AA0403, and RESID:AA0515 for other O-glycosylated threonines.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptide-O-fucosyltransferase (EC 2.4.1.221)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>T</SequenceSpec>
-<Xref>PSI-MOD:00813</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__o-linked (fuc) threonine__t">CARBOHYD O-linked (Fuc) threonine</Feature>
-<Feature type="UniProt" key="carbohyd__o-linked (fuc...) threonine__t">CARBOHYD O-linked (Fuc...) threonine</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="carbohyd__o-linked (dhex) threonine__t">CARBOHYD O-linked (dHex) threonine</Feature>
-<Note>this UniProt feature is used when the identity of the sugar has not been determined</Note>
-</FeatureNote>
-<FeatureNote>
-<Feature type="UniProt" key="carbohyd__o-linked (dhex...) threonine__t">CARBOHYD O-linked (dHex...) threonine</Feature>
-<Note>this UniProt feature is used when the identity of the sugar has not been determined</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0405.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0405.PDB" />
-</Entry>
-<Entry id="AA0406">
-<Header>
-<Code>AA0406</Code>
-<Dates>
-<CreationDate>31-Mar-2006</CreationDate>
-<StrucRevDate>31-Mar-2006</StrucRevDate>
-<TextChngDate>20-Apr-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-xylosyl-L-serine</Name>
-<AlternateName>O-(beta-D-xylopyranosyl)-L-serine</AlternateName>
-<AlternateName>O-glycosylserine</AlternateName>
-<AlternateName>O3-xylosylserine</AlternateName>
-<SystematicName>(2S)-2-amino-3-(alpha-D-xylopyranosyloxy)propanoic acid</SystematicName>
-<Xref>CAS:6050-71-1</Xref>
-<Xref>PDBHET:XYS</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 8 H 13 N 1 O 6</Formula>
-<Weight type="chemical">219.19</Weight>
-<Weight type="physical">219.074287</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 5 H 8 N 0 O 4</Formula>
-<Weight type="chemical">132.12</Weight>
-<Weight type="physical">132.042259</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sundaramoorthy, M.</Author>
-<Author>Terner, J.</Author>
-<Author>Poulos, T.L.</Author>
-</Authors>
-<Citation>Structure 3, 1367-1377, 1995</Citation>
-<Title>The crystal structure of chloroperoxidase: a heme peroxidase--cytochrome P450 functional hybrid.</Title>
-<Xref>DOI:10.1016/S0969-2126(01)00274-X</Xref>
-<Xref>PMID:8747463</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sundaramoorthy, M.</Author>
-<Author>Poulos, T.L.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, February 1996</Citation>
-<Description>Chloroperoxidase.</Description>
-<Xref>PDB:1CPO</Xref>
-<Note>X-ray diffraction, 1.9 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sundaramoorthy, M.</Author>
-<Author>Poulos, T.L.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, February 1996</Citation>
-<Description>Chloroperoxidase.</Description>
-<Xref>PDB:2CPO</Xref>
-<Note>X-ray diffraction, 2.16 angstroms</Note>
-</ReferenceBlock>
-<Comment>One glycosylated serine with weak electron density was modeled as O3-alpha-xylosylserine, while O3-alpha-mannosyl serine and threonine were modeled at ten other positions. The authors do not discuss this exception or provide chemical evidence for it. Since an O3-xylosyl serine modification has not been reported in any other fungal proteins, the modification is probably also an O3-alpha-mannosyl serine (see RESID:AA0402).</Comment>
-<Comment>See also RESID:AA0154, RESID:AA0208, RESID:AA0209, RESID:AA0210, RESID:AA0291, RESID:AA0296, RESID:AA0297, RESID:AA0397, RESID:AA0398, RESID:AA0400, RESID:AA0402, RESID:AA0404, and RESID:AA0422 for other O-glycosylated serines.</Comment>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>PSI-MOD:00814</Xref>
-</SequenceCode>
-<Source>deprecated</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this dubious modification is not currently annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0406.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0406.PDB" />
-</Entry>
-<Entry id="AA0407">
-<Header>
-<Code>AA0407</Code>
-<Dates>
-<CreationDate>31-Mar-2006</CreationDate>
-<StrucRevDate>31-Mar-2006</StrucRevDate>
-<TextChngDate>30-Sep-2008</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-stearoyl-L-cysteine</Name>
-<AlternateName>2-amino-3-(octadecanoylthio)propanoic acid</AlternateName>
-<AlternateName>cysteine octadecanoate thioester</AlternateName>
-<AlternateName>cysteine stearate thioester</AlternateName>
-<SystematicName>(R)-2-amino-3-(octadecanoylsulfanyl)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 21 H 39 N 1 O 2 S 1</Formula>
-<Weight type="chemical">369.61</Weight>
-<Weight type="physical">369.270150</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 18 H 34 N 0 O 1 S 0</Formula>
-<Weight type="chemical">266.47</Weight>
-<Weight type="physical">266.260966</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Schmidt, M.</Author>
-<Author>Schmidt, M.F.</Author>
-<Author>Rott, R.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 263, 18635-18639, 1988</Citation>
-<Title>Chemical identification of cysteine as palmitoylation site in a transmembrane protein (Semliki Forest virus E1).</Title>
-<Xref>PMID:3143715</Xref>
-<Note>misidentification of modification as S-palmitoyl cysteine after use of radiolabeled palmitate without accounting for metabolic conversion</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bach, R.</Author>
-<Author>Konigsberg, W.H.</Author>
-<Author>Nemerson, Y.</Author>
-</Authors>
-<Citation>Biochemistry 27, 4227-4231, 1988</Citation>
-<Title>Human tissue factor contains thioester-linked palmitate and stearate on the cytoplasmic half-cystine.</Title>
-<Xref>DOI:10.1021/bi00412a004</Xref>
-<Xref>PMID:3166978</Xref>
-<Note>identification of modification produced by an enzyme with relaxed specificity</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Veit, M.</Author>
-<Author>Herrler, G.</Author>
-<Author>Schmidt, M.F.</Author>
-<Author>Rott, R.</Author>
-<Author>Klenk, H.D.</Author>
-</Authors>
-<Citation>Virology 177, 807-811, 1990</Citation>
-<Title>The hemagglutinating glycoproteins of influenza B and C viruses are acylated with different fatty acids.</Title>
-<Xref>DOI:10.1016/0042-6822(90)90554-5</Xref>
-<Xref>PMID:2371783</Xref>
-<Note>recognition of preferential modification formation of S-stearoyl cysteine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Veit, M.</Author>
-<Author>Reverey, H.</Author>
-<Author>Schmidt, M.F.</Author>
-</Authors>
-<Citation>Biochem. J. 318, 163-172, 1996</Citation>
-<Title>Cytoplasmic tail length influences fatty acid selection for acylation of viral glycoproteins.</Title>
-<Xref>PMID:8761467</Xref>
-<Note>chemical characterization; examines conditions for selection of stearate in preference to palmitate</Note>
-</ReferenceBlock>
-<Comment>Although the predominant palmitoyl transferase in mammalian systems appears to utilize a mixture of saturated and unsaturated fatty acids, some systems may be more specific in their incorporation of other fatty acids.  See RESID:AA0307 and RESID:AA0308.</Comment>
-<Comment>This modification may be misidentified as S-palmitoyl-cysteine (see RESID:AA0106) when labeled palmitate is used without determining whether metabolic conversion has occurred.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>protein-cysteine S-stearoyltransferase (EC 2.3.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>PSI-MOD:00816</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lipoprotein</Keyword>
-<Keyword>stearate</Keyword>
-<Keyword>thioester bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__s-stearoyl cysteine__c">LIPID S-stearoyl cysteine</Feature>
-</Features>
-<Image src="/images/AA0407.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0407.PDB" />
-</Entry>
-<Entry id="AA0408">
-<Header>
-<Code>AA0408</Code>
-<Dates>
-<CreationDate>31-Mar-2006</CreationDate>
-<StrucRevDate>31-Mar-2006</StrucRevDate>
-<TextChngDate>31-Dec-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>3'-geranyl-2',3'-dihydro-2',N2-cyclo-L-tryptophan</Name>
-<AlternateName>(2S,3R)-3-geranyl-2,3-dihydro-2,N(alpha)-cyclo-L-tryptophan</AlternateName>
-<SystematicName>(2S,3aR,8aS)-3a-[(2E)-3,7-dimethylocta-2,6-dien-1-yl]-1,2,3,3a,8,8a-hexahydropyrrolo[2,3-b]indole-2-carboxylic acid</SystematicName>
-<Xref>ChEBI:35304</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 21 H 26 N 2 O 1</Formula>
-<Weight type="chemical">322.45</Weight>
-<Weight type="physical">322.204513</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0018">
-<Formula>C 10 H 16 N 0 O 0</Formula>
-<Weight type="chemical">136.24</Weight>
-<Weight type="physical">136.125201</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Magnuson, R.</Author>
-<Author>Solomon, J.</Author>
-<Author>Grossman, A.D.</Author>
-</Authors>
-<Citation>Cell 77, 207-216, 1994</Citation>
-<Title>Biochemical and genetic characterization of a competence pheromone from B. subtilis.</Title>
-<Xref>DOI:10.1016/0092-8674(94)90313-1</Xref>
-<Xref>PMID:8168130</Xref>
-<Note>peptide structure and identification as a tryptophan modification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Okada, M.</Author>
-<Author>Sato, I.</Author>
-<Author>Cho, S.J.</Author>
-<Author>Iwata, H.</Author>
-<Author>Nishio, T.</Author>
-<Author>Dubnau, D.</Author>
-<Author>Sakagami, Y.</Author>
-</Authors>
-<Citation>Nature Chem. Biol. 1, 23-24, 2005</Citation>
-<Title>Structure of the Bacillus subtilis quorum-sensing peptide pheromone ComX.</Title>
-<Xref>DOI:10.1038/nchembio709</Xref>
-<Xref>PMID:16407988</Xref>
-<Note>mass spectrographic, (1)H-NMR, DQF-COSY, and ROESY identification; chemical synthesis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Okada, M.</Author>
-</Authors>
-<Citation>Biosci. Biotechnol. Biochem. 75, 1413-1417, 2011</Citation>
-<Title>Post-translational isoprenylation of tryptophan.</Title>
-<Xref>PMID:21821957</Xref>
-<Note>review article</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>W</SequenceSpec>
-<Xref>PSI-MOD:00817</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lipoprotein</Keyword>
-<Keyword>prenylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__3&apos;-geranyl-2&apos;,n2-cyclotryptophan__w">LIPID 3'-geranyl-2',N2-cyclotryptophan</Feature>
-</Features>
-<Image src="/images/AA0408.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0408.PDB" />
-</Entry>
-<Entry id="AA0409">
-<Header>
-<Code>AA0409</Code>
-<Dates>
-<CreationDate>26-May-2006</CreationDate>
-<StrucRevDate>26-May-2006</StrucRevDate>
-<TextChngDate>25-Feb-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-2-aminobutanoic acid</Name>
-<AlternateName>L-2-amino-n-butyric acid</AlternateName>
-<AlternateName>L-2-aminobutyric acid</AlternateName>
-<AlternateName>L-alpha-amino-n-butyric acid</AlternateName>
-<AlternateName>L-alpha-aminobutyric acid</AlternateName>
-<AlternateName>L-butyrine</AlternateName>
-<SystematicName>(S)-2-aminobutanoic acid</SystematicName>
-<Xref>CAS:1492-24-6</Xref>
-<Xref>ChEBI:35619</Xref>
-<Xref>PDBHET:ABA</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 7 N 1 O 1</Formula>
-<Weight type="chemical">85.11</Weight>
-<Weight type="physical">85.052764</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0006">
-<Formula>C -1 H 0 N 0 O -2</Formula>
-<Weight type="chemical">-44.01</Weight>
-<Weight type="physical">-43.989829</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>van Thor, J.J.</Author>
-<Author>Gensch, T.</Author>
-<Author>Hellingwerf, K.J.</Author>
-<Author>Johnson, L.N.</Author>
-</Authors>
-<Citation>Nature Struct. Biol. 9, 37-41, 2002</Citation>
-<Title>Phototransformation of green fluorescent protein with UV and visible light leads to decarboxylation of glutamate 222.</Title>
-<Xref>DOI:10.1038/nsb739</Xref>
-<Xref>PMID:11740505</Xref>
-<Note>X-ray diffraction, 1.80 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>van Thor, J.J.</Author>
-<Author>Gensch, T.</Author>
-<Author>Hellingwerf, K.J.</Author>
-<Author>Johnson, L.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, May 2001</Citation>
-<Description>Photoproduct of the wild-type Aequorea victoria green fluorescent protein.</Description>
-<Xref>PDB:1HCJ</Xref>
-<Note>X-ray diffraction, 1.80 angstroms; the modification is mentioned in the PDB entry but is presented as glutamic acid</Note>
-</ReferenceBlock>
-<Comment>Exposure of green fluorescent protein to 254 nm UV light or to 390 nm visible light causes gamma decarboxylation of glutamic acid 222.</Comment>
-<Comment>Unlike the threonine in 3-methylanthionine, the L configuration (S chirality) of the 2-aminobutanoate skeleton is maintained.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>E</SequenceSpec>
-<Condition>incidental to RESID:AA0183</Condition>
-<Condition>incidental to RESID:AA0184</Condition>
-<Xref>PSI-MOD:00819</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0409.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0409.PDB" />
-</Entry>
-<Entry id="AA0410">
-<Header>
-<Code>AA0410</Code>
-<Dates>
-<CreationDate>26-May-2006</CreationDate>
-<StrucRevDate>26-May-2006</StrucRevDate>
-<TextChngDate>20-May-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>2-imino-alanine 5-imidazolinone glycine</Name>
-<AlternateName>2,N-didehydroalanyl-5-imidazolinone glycine</AlternateName>
-<AlternateName>2-(1-iminoethyl)-1-carboxymethyl-1-imidazolin-5-one</AlternateName>
-<AlternateName>2-imino-alanyl-5-imidazolinone glycine</AlternateName>
-<AlternateName>alanyl-5-imidazolinone glycine</AlternateName>
-<AlternateName>para-hydroxybenzylidene-imidazolidinone chromophore</AlternateName>
-<AlternateName>red fluorescent protein zRFP574 chromophore</AlternateName>
-<AlternateName>[2-(1-iminoethyl)-5-oxo-4,5-dihydro-imidazol-1-yl]-acetic acid</AlternateName>
-<SystematicName>(2-ethanimidoyl-5-oxo-4,5-dihydro-1H-imidazol-1-yl)acetic acid</SystematicName>
-<Xref>PDBHET:XYG</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 4 N 2 O 1</Formula>
-<Weight type="chemical">108.10</Weight>
-<Weight type="physical">108.032363</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0004 AA0008">
-<Formula>C -1 H -4 N 0 O -3</Formula>
-<Weight type="chemical">-64.04</Weight>
-<Weight type="physical">-64.016044</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Pletneva, N.</Author>
-<Author>Pletnev, S.</Author>
-<Author>Tikhonova, T.</Author>
-<Author>Popov, V.</Author>
-<Author>Martynov, V.</Author>
-<Author>Pletnev, V.</Author>
-</Authors>
-<Citation>Acta Crystallogr. D Biol. Crystallogr. 62, 527-532, 2006</Citation>
-<Title>Structure of a red fluorescent protein from Zoanthus, zRFP574, reveals a novel chromophore.</Title>
-<Xref>DOI:10.1107/S0907444906007852</Xref>
-<Xref>PMID:16627946</Xref>
-<Note>the authors have not published the sequence</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Pletneva, N.</Author>
-<Author>Pletnev, S.</Author>
-<Author>Tikhonova, T.</Author>
-<Author>Popov, V.</Author>
-<Author>Martynov, V.</Author>
-<Author>Pletnev, V.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, January 2006</Citation>
-<Description>Crystal structure of red fluorescent protein from Zoanthus, zRFP574, at 2.4 A resolution.</Description>
-<Xref>PDB:2FL1</Xref>
-<Note>X-ray diffraction, 2.40 angstroms</Note>
-</ReferenceBlock>
-<Comment>This entry represents the cross-link of the peptide backbone from the alpha-carboxyl carbon of residue N, an aspartic acid, to the alpha-amino nitrogen of residue N+2, a glycine, coupled with the formation of a double bond to the alpha-amino nitrogen of residue N, the loss of a molecule of water, and the beta-decarboxylation of the aspartic acid.</Comment>
-<Comment>This cross-link is accompanied by modification of residue N+1. The modified residue N+1 is presented in a separate entry and is not included in the mass accounting of this entry. The backbone atoms of residue N+1 are shown in gray in the diagram.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>D, G</SequenceSpec>
-<Condition>carboxamidine</Condition>
-<Condition>cross-link 1</Condition>
-<Condition>incidental to RESID:AA0183</Condition>
-<Condition>incidental to RESID:AA0365</Condition>
-<Xref>PSI-MOD:00820</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chromoprotein</Keyword>
-<Keyword>imidazolinone/oxazolinone ring</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0410.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0410.PDB" />
-</Entry>
-<Entry id="AA0411">
-<Header>
-<Code>AA0411</Code>
-<Dates>
-<CreationDate>26-May-2006</CreationDate>
-<StrucRevDate>26-May-2006</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-(L-alanyl)-L-cysteine</Name>
-<AlternateName>alanine cysteine thioester</AlternateName>
-<AlternateName>S-(2-aminopropanoyl)cysteine</AlternateName>
-<SystematicName>(2R)-2-amino-3-([(2S)-2-aminopropanoyl]sulfanyl)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 9 N 2 O 2 S 1</Formula>
-<Weight type="chemical">173.21</Weight>
-<Weight type="physical">173.038474</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0001 AA0005">
-<Formula>C 0 H -2 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Dufour, P.</Author>
-<Author>Jarraud, S.</Author>
-<Author>Vandenesch, F.</Author>
-<Author>Greenland, T.</Author>
-<Author>Novick, R.P.</Author>
-<Author>Bes, M.</Author>
-<Author>Etienne, J.</Author>
-<Author>Lina, G.</Author>
-</Authors>
-<Citation>J. Bacteriol. 184, 1180-1186, 2002</Citation>
-<Title>High genetic variability of the agr locus in Staphylococcus species.</Title>
-<Xref>DOI:10.1128/jb.184.4.1180-1186.2002</Xref>
-<Xref>PMID:11807079</Xref>
-</ReferenceBlock>
-<Comment>These are thioester cross-links formed between cysteine residues and the alanine carboxyl end of a peptide.</Comment>
-<Comment>This modification is predicted for proteins homologous to autoinducing peptides in certain organisms where the position corresponding to the carboxyl end encodes alanine.</Comment>
-<SequenceCode>
-<SequenceSpec>A, C</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:00821</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>thioester bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__alanyl cysteine thioester (cys-ala)__c__a">CROSSLNK Alanyl cysteine thioester (Cys-Ala)</Feature>
-</Features>
-<Image src="/images/AA0411.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0411.PDB" />
-</Entry>
-<Entry id="AA0412">
-<Header>
-<Code>AA0412</Code>
-<Dates>
-<CreationDate>26-May-2006</CreationDate>
-<StrucRevDate>26-May-2006</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-(L-leucyl)-L-cysteine</Name>
-<AlternateName>leucine cysteine thioester</AlternateName>
-<AlternateName>S-(2-amino-4-methylpentanoyl)cysteine</AlternateName>
-<SystematicName>(2R)-2-amino-3-([(2S)-2-amino-4-methylpentanoyl]sulfanyl)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 15 N 2 O 2 S 1</Formula>
-<Weight type="chemical">215.29</Weight>
-<Weight type="physical">215.085424</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0011">
-<Formula>C 0 H -2 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kalkum, M.</Author>
-<Author>Lyon, G.J.</Author>
-<Author>Chait, B.T.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 100, 2795-2800, 2003</Citation>
-<Title>Detection of secreted peptides by using hypothesis-driven multistage mass spectrometry.</Title>
-<Xref>DOI:10.1073/pnas.0436605100</Xref>
-<Xref>PMID:12591958</Xref>
-</ReferenceBlock>
-<Comment>These are thioester cross-links formed between cysteine residues and the leucine carboxyl end of a peptide.</Comment>
-<SequenceCode>
-<SequenceSpec>C, L</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:00822</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>thioester bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__leucyl cysteine thioester (cys-leu)__c__l">CROSSLNK Leucyl cysteine thioester (Cys-Leu)</Feature>
-</Features>
-<Image src="/images/AA0412.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0412.PDB" />
-</Entry>
-<Entry id="AA0413">
-<Header>
-<Code>AA0413</Code>
-<Dates>
-<CreationDate>26-May-2006</CreationDate>
-<StrucRevDate>26-May-2006</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-(L-methionyl)-L-cysteine</Name>
-<AlternateName>methionine cysteine thioester</AlternateName>
-<AlternateName>S-(2-amino-4-methylthiobutanoyl)cysteine</AlternateName>
-<SystematicName>(2R)-2-amino-3-([(2S)-2-amino-4-(methylsulfanyl)butanoyl]sulfanyl)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 8 H 13 N 2 O 2 S 2</Formula>
-<Weight type="chemical">233.32</Weight>
-<Weight type="physical">233.041845</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0013">
-<Formula>C 0 H -2 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lyon, G.J.</Author>
-<Author>Wright, J.S.</Author>
-<Author>Muir, T.W.</Author>
-<Author>Novick, R.P.</Author>
-</Authors>
-<Citation>Biochemistry 41, 10095-10104, 2002</Citation>
-<Title>Key determinants of receptor activation in the agr autoinducing peptides of Staphylococcus aureus.</Title>
-<Xref>DOI:10.1021/bi026049u</Xref>
-<Xref>PMID:12146974</Xref>
-</ReferenceBlock>
-<Comment>These are thioester cross-links formed between cysteine residues and the methionine carboxyl end of a peptide.</Comment>
-<SequenceCode>
-<SequenceSpec>C, M</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:00823</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>thioester bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__methionyl cysteine thioester (cys-met)__c__m">CROSSLNK Methionyl cysteine thioester (Cys-Met)</Feature>
-</Features>
-<Image src="/images/AA0413.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0413.PDB" />
-</Entry>
-<Entry id="AA0414">
-<Header>
-<Code>AA0414</Code>
-<Dates>
-<CreationDate>26-May-2006</CreationDate>
-<StrucRevDate>26-May-2006</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-(L-phenylalanyl)-L-cysteine</Name>
-<AlternateName>phenylalanine cysteine thioester</AlternateName>
-<AlternateName>S-(2-amino-3-phenylpropanoyl)cysteine</AlternateName>
-<SystematicName>(2R)-2-amino-3-([(2S)-2-amino-3-phenylpropanoyl]sulfanyl)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 12 H 13 N 2 O 2 S 1</Formula>
-<Weight type="chemical">249.31</Weight>
-<Weight type="physical">249.069774</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0014">
-<Formula>C 0 H -2 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kalkum, M.</Author>
-<Author>Lyon, G.J.</Author>
-<Author>Chait, B.T.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 100, 2795-2800, 2003</Citation>
-<Title>Detection of secreted peptides by using hypothesis-driven multistage mass spectrometry.</Title>
-<Xref>DOI:10.1073/pnas.0436605100</Xref>
-<Xref>PMID:12591958</Xref>
-</ReferenceBlock>
-<Comment>These are thioester cross-links formed between cysteine residues and the phenylalanine carboxyl end of a peptide.</Comment>
-<SequenceCode>
-<SequenceSpec>C, F</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:00825</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>thioester bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__phenylalanyl cysteine thioester (cys-phe)__c__f">CROSSLNK Phenylalanyl cysteine thioester (Cys-Phe)</Feature>
-</Features>
-<Image src="/images/AA0414.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0414.PDB" />
-</Entry>
-<Entry id="AA0415">
-<Header>
-<Code>AA0415</Code>
-<Dates>
-<CreationDate>26-May-2006</CreationDate>
-<StrucRevDate>26-May-2006</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-(L-threonyl)-L-cysteine</Name>
-<AlternateName>S-(2-amino-3-hydroxybutanoyl)cysteine</AlternateName>
-<AlternateName>threonine cysteine thioester</AlternateName>
-<SystematicName>(2R)-2-amino-3-([(2S,3R)-2-amino-3-hydroxybutanoyl]sulfanyl)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 11 N 2 O 3 S 1</Formula>
-<Weight type="chemical">203.24</Weight>
-<Weight type="physical">203.049038</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0017">
-<Formula>C 0 H -2 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sakinc, T.</Author>
-<Author>Kulczak, P.</Author>
-<Author>Henne, K.</Author>
-<Author>Gatermann, S.G.</Author>
-</Authors>
-<Citation>FEMS Microbiol. Lett. 237, 157-161, 2004</Citation>
-<Title>Cloning of an agr homologue of Staphylococcus saprophyticus.</Title>
-<Xref>DOI:10.1016/j.femsle.2004.06.030</Xref>
-<Xref>PMID:15268951</Xref>
-</ReferenceBlock>
-<Comment>These are thioester cross-links formed between cysteine residues and the threonine carboxyl end of a peptide.</Comment>
-<Comment>This modification is predicted for proteins homologous to autoinducing peptides in certain organisms where the position corresponding to the carboxyl end encodes threonine.</Comment>
-<SequenceCode>
-<SequenceSpec>C, T</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:00826</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>thioester bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__threonyl cysteine thioester (cys-thr)__c__t">CROSSLNK Threonyl cysteine thioester (Cys-Thr)</Feature>
-</Features>
-<Image src="/images/AA0415.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0415.PDB" />
-</Entry>
-<Entry id="AA0416">
-<Header>
-<Code>AA0416</Code>
-<Dates>
-<CreationDate>26-May-2006</CreationDate>
-<StrucRevDate>26-May-2006</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-(L-tyrosyl)-L-cysteine</Name>
-<AlternateName>S-[2-amino-3-(4-hydoxyphenyl)propanoyl]cysteine</AlternateName>
-<AlternateName>tyrosine cysteine thioester</AlternateName>
-<SystematicName>(2R)-2-amino-3-([(2S)-2-amino-3-(4-hydroxyphenyl)propanoyl]sulfanyl)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 12 H 13 N 2 O 3 S 1</Formula>
-<Weight type="chemical">265.31</Weight>
-<Weight type="physical">265.064688</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0019">
-<Formula>C 0 H -2 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Dufour, P.</Author>
-<Author>Jarraud, S.</Author>
-<Author>Vandenesch, F.</Author>
-<Author>Greenland, T.</Author>
-<Author>Novick, R.P.</Author>
-<Author>Bes, M.</Author>
-<Author>Etienne, J.</Author>
-<Author>Lina, G.</Author>
-</Authors>
-<Citation>J. Bacteriol. 184, 1180-1186, 2002</Citation>
-<Title>High genetic variability of the agr locus in Staphylococcus species.</Title>
-<Xref>DOI:10.1128/jb.184.4.1180-1186.2002</Xref>
-<Xref>PMID:11807079</Xref>
-</ReferenceBlock>
-<Comment>These are thioester cross-links formed between cysteine residues and the tyrosine carboxyl end of a peptide.</Comment>
-<Comment>This modification is predicted for proteins homologous to autoinducing peptides in certain organisms where the position corresponding to the carboxyl end encodes tyrosine.</Comment>
-<SequenceCode>
-<SequenceSpec>C, Y</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:00827</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>thioester bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__tyrosyl cysteine thioester (cys-tyr)__c__y">CROSSLNK Tyrosyl cysteine thioester (Cys-Tyr)</Feature>
-</Features>
-<Image src="/images/AA0416.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0416.PDB" />
-</Entry>
-<Entry id="AA0417">
-<Header>
-<Code>AA0417</Code>
-<Dates>
-<CreationDate>26-May-2006</CreationDate>
-<StrucRevDate>26-May-2006</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-(L-tryptophanyl)-L-cysteine</Name>
-<AlternateName>S-[2-amino-3-(1H-indol-3-yl)propanoyl]cysteine</AlternateName>
-<AlternateName>tryptophan cysteine thioester</AlternateName>
-<SystematicName>(2R)-2-amino-3-([(2S)-2-amino-3-(1H-indol-3-yl)propanoyl]sulfanyl)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 14 H 14 N 3 O 2 S 1</Formula>
-<Weight type="chemical">288.35</Weight>
-<Weight type="physical">288.080673</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0018">
-<Formula>C 0 H -2 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sturme, M.H.</Author>
-<Author>Nakayama, J.</Author>
-<Author>Molenaar, D.</Author>
-<Author>Murakami, Y.</Author>
-<Author>Kunugi, R.</Author>
-<Author>Fujii, T.</Author>
-<Author>Vaughan, E.E.</Author>
-<Author>Kleerebezem, M.</Author>
-<Author>de Vos, W.M.</Author>
-</Authors>
-<Citation>J. Bacteriol. 187, 5224-5235, 2005</Citation>
-<Title>An agr-like two-component regulatory system in Lactobacillus plantarum is involved in production of a novel cyclic peptide and regulation of adherence.</Title>
-<Xref>DOI:10.1128/JB.187.15.5224-5235.2005</Xref>
-<Xref>PMID:16030216</Xref>
-</ReferenceBlock>
-<Comment>These are thioester cross-links formed between cysteine residues and the tryptophan carboxyl end of a peptide.</Comment>
-<SequenceCode>
-<SequenceSpec>C, W</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:00828</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>thioester bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__tryptophanyl cysteine thioester (cys-trp)__c__w">CROSSLNK Tryptophanyl cysteine thioester (Cys-Trp)</Feature>
-</Features>
-<Image src="/images/AA0417.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0417.PDB" />
-</Entry>
-<Entry id="AA0418">
-<Header>
-<Code>AA0418</Code>
-<Dates>
-<CreationDate>26-May-2006</CreationDate>
-<StrucRevDate>26-May-2006</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-(L-phenylalanyl)-L-serine</Name>
-<AlternateName>O-(2-amino-3-phenylpropanoyl)serine</AlternateName>
-<AlternateName>phenylalanine serine ester</AlternateName>
-<SystematicName>(2S)-2-amino-3-([(2S)-2-amino-3-phenylpropanoyl]oxy)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 12 H 13 N 2 O 3</Formula>
-<Weight type="chemical">233.25</Weight>
-<Weight type="physical">233.092617</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0014 AA0016">
-<Formula>C 0 H -2 N 0 O -1</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kalkum, M.</Author>
-<Author>Lyon, G.J.</Author>
-<Author>Chait, B.T.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 100, 2795-2800, 2003</Citation>
-<Title>Detection of secreted peptides by using hypothesis-driven multistage mass spectrometry.</Title>
-<Xref>DOI:10.1073/pnas.0436605100</Xref>
-<Xref>PMID:12591958</Xref>
-</ReferenceBlock>
-<Comment>These are ester cross-links formed between serine residues and the phenylalanine carboxyl end of a peptide.</Comment>
-<SequenceCode>
-<SequenceSpec>F, S</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:00829</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__phenylalanyl serine ester (ser-phe)__s__f">CROSSLNK Phenylalanyl serine ester (Ser-Phe)</Feature>
-</Features>
-<Image src="/images/AA0418.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0418.PDB" />
-</Entry>
-<Entry id="AA0419">
-<Header>
-<Code>AA0419</Code>
-<Dates>
-<CreationDate>26-May-2006</CreationDate>
-<StrucRevDate>26-May-2006</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-methyl-L-proline</Name>
-<AlternateName>1-methylpyrrolidine-2-carboxylic acid</AlternateName>
-<AlternateName>hygric acid</AlternateName>
-<SystematicName>(S)-1-methylpyrrolidine-2-carboxylic acid</SystematicName>
-<Xref>CAS:475-11-6</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 10 N 1 O 1</Formula>
-<Weight type="chemical">112.15</Weight>
-<Weight type="physical">112.076239</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0015">
-<Formula>C 1 H 2 N 0 O 0</Formula>
-<Weight type="chemical">14.03</Weight>
-<Weight type="physical">14.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Desrosiers, R.</Author>
-<Author>Tanguay, R.M.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 263, 4686-4692, 1988</Citation>
-<Title>Methylation of Drosophila histones at proline, lysine, and arginine residues during heat shock.</Title>
-<Xref>PMID:3127388</Xref>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>N-terminal RCC1 methyltransferase</EnzymeName>
-<EnzymeName>protein N-terminal methyltransferase</EnzymeName>
-<EnzymeName>S-adenosyl-L-methionine:N-terminal-(A,P,S)PK-[protein] methyltransferase (EC 2.1.1.244)</EnzymeName>
-<EnzymeName>protein N-terminal monomethyltransferase</EnzymeName>
-<EnzymeName>S-adenosyl-L-methionine:N-terminal-(A,P,S)PK-[protein] monomethyltransferase (EC 2.1.1.299)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>P</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0035568</Xref>
-<Xref>PSI-MOD:00830</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-<Keyword>methylated amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n-methylproline__p">MOD_RES N-methylproline</Feature>
-</Features>
-<Image src="/images/AA0419.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0419.PDB" />
-</Entry>
-<Entry id="AA0420">
-<Header>
-<Code>AA0420</Code>
-<Dates>
-<CreationDate>26-May-2006</CreationDate>
-<StrucRevDate>26-May-2006</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N4-(N-acetylamino)galactosyl-L-asparagine</Name>
-<AlternateName>N4-(2-acetamido-2-deoxy-beta-D-galactopyranosyl)-L-asparagine</AlternateName>
-<AlternateName>N4-(2-acetylamino-2-deoxy-beta-D-galactopyranosyl)-L-asparagine</AlternateName>
-<AlternateName>N4-(N-acetylgalactosaminyl)asparagine</AlternateName>
-<AlternateName>N4-asparagine-beta-N-acetylgalactosaminide</AlternateName>
-<AlternateName>N4-glycosyl-L-asparagine</AlternateName>
-<AlternateName>N4-glycosylasparagine</AlternateName>
-<SystematicName>(2S)-2-amino-4-(2-acetamido-2-deoxy-beta-D-galactopyranosyl)amino-4-oxobutanoic acid</SystematicName>
-<Xref>CAS:100991-94-4</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 12 H 19 N 3 O 7 +</Formula>
-<Weight type="chemical">317.30 +</Weight>
-<Weight type="physical">317.122300 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0003">
-<Formula>C 8 H 13 N 1 O 5 +</Formula>
-<Weight type="chemical">203.19 +</Weight>
-<Weight type="physical">203.079373 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kaercher, U.</Author>
-<Author>Schroeder, H.</Author>
-<Author>Haslinger, E.</Author>
-<Author>Allmaier, G.</Author>
-<Author>Schreiner, R.</Author>
-<Author>Wieland, F.</Author>
-<Author>Haselbeck, A.</Author>
-<Author>Koenig, H.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 268, 26821-26826, 1993</Citation>
-<Title>Primary structure of the heterosaccharide of the surface glycoprotein of Methanothermus fervidus.</Title>
-<Xref>PMID:8262914</Xref>
-<Note>probably an alpha-N-glycosidic linkage</Note>
-</ReferenceBlock>
-<Comment>This modification occurs in archaebacterial cell surface proteins with an NX[ST] motif.</Comment>
-<Comment>See also RESID:AA0151 and RESID:AA0421 for other N4-glycosylated asparagines.</Comment>
-<SequenceCode>
-<SequenceSpec>N</SequenceSpec>
-<Xref>PSI-MOD:00832</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__n-linked (galnac...) asparagine__n">CARBOHYD N-linked (GalNAc...) asparagine</Feature>
-<Feature type="UniProt" key="carbohyd__n-linked (galnac...) (glycosaminoglycan) asparagine__n">CARBOHYD N-linked (GalNAc...) (glycosaminoglycan) asparagine</Feature>
-</Features>
-<Image src="/images/AA0420.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0420.PDB" />
-</Entry>
-<Entry id="AA0421">
-<Header>
-<Code>AA0421</Code>
-<Dates>
-<CreationDate>26-May-2006</CreationDate>
-<StrucRevDate>26-May-2006</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N4-glucosyl-L-asparagine</Name>
-<AlternateName>N4-(D-glucopyranosyl)-L-asparagine</AlternateName>
-<AlternateName>N4-(D-glucopyranosyl)-L-asparagine</AlternateName>
-<AlternateName>N4-asparagine-glucoside</AlternateName>
-<AlternateName>N4-glucosylasparagine</AlternateName>
-<AlternateName>N4-glycosyl-L-asparagine</AlternateName>
-<AlternateName>N4-glycosylasparagine</AlternateName>
-<SystematicName>(2S)-2-amino-4-(D-glucopyranosyl)amino-4-oxobutanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 10 H 16 N 2 O 7 +</Formula>
-<Weight type="chemical">276.25 +</Weight>
-<Weight type="physical">276.095751 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0003">
-<Formula>C 6 H 10 N 0 O 5 +</Formula>
-<Weight type="chemical">162.14 +</Weight>
-<Weight type="physical">162.052823 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Shibata, S.</Author>
-<Author>Takeda, T.</Author>
-<Author>Natori, Y.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 263, 12483-12485, 1988</Citation>
-<Title>The structure of nephritogenoside. A nephritogenic glycopeptide with alpha-N-glycosidic linkage.</Title>
-<Xref>PMID:3410849</Xref>
-<Note>glycopeptide with trisaccharide glucose attached by an alpha-N-glycosidic linkage, and the NX[ST] motif is not present</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mengele, R.</Author>
-<Author>Sumper, M.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 267, 8182-8185, 1992</Citation>
-<Title>Drastic differences in glycosylation of related S-layer glycoproteins from moderate and extreme halophiles.</Title>
-<Xref>PMID:1569073</Xref>
-<Note>the anomeric form was not determined</Note>
-</ReferenceBlock>
-<Comment>The alpha anomeric form is shown.</Comment>
-<Comment>See also RESID:AA0151 and RESID:AA0420 for other N4-glycosylated asparagines.</Comment>
-<SequenceCode>
-<SequenceSpec>N</SequenceSpec>
-<Xref>PSI-MOD:00833</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__n-linked (glc) asparagine__n">CARBOHYD N-linked (Glc) asparagine</Feature>
-<Feature type="UniProt" key="carbohyd__n-linked (glc...) asparagine__n">CARBOHYD N-linked (Glc...) asparagine</Feature>
-</Features>
-<Image src="/images/AA0421.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0421.PDB" />
-</Entry>
-<Entry id="AA0422">
-<Header>
-<Code>AA0422</Code>
-<Dates>
-<CreationDate>26-May-2006</CreationDate>
-<StrucRevDate>26-May-2006</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-(N-acetylamino)fucosyl-L-serine</Name>
-<AlternateName>O-(2-acetylamino-2-deoxy-beta-D-fucopyranosyl)-L-serine</AlternateName>
-<AlternateName>O-(N-acetylfucosaminyl)serine</AlternateName>
-<AlternateName>O-seryl-beta-N-acetylfucosaminide</AlternateName>
-<AlternateName>O3-(2-acetamido-2-deoxy-beta-D-fucopyranosyl)-L-serine</AlternateName>
-<AlternateName>O3-(N-acetylfucosaminyl)serine</AlternateName>
-<SystematicName>(2S)-2-amino-3-(2-acetamido-2-deoxy-beta-D-fucopyranosyloxy)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 11 H 18 N 2 O 6</Formula>
-<Weight type="chemical">274.27</Weight>
-<Weight type="physical">274.116486</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 8 H 13 N 1 O 4</Formula>
-<Weight type="chemical">187.19</Weight>
-<Weight type="physical">187.084458</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Castric, P.</Author>
-<Author>Cassels, F.J.</Author>
-<Author>Carlson, R.W.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 276, 26479-26485, 2001</Citation>
-<Title>Structural characterization of the Pseudomonas aeruginosa 1244 pilin glycan.</Title>
-<Xref>DOI:10.1074/jbc.M102685200</Xref>
-<Xref>PMID:11342554</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Comer, J.E.</Author>
-<Author>Marshall, M.A.</Author>
-<Author>Blanch, V.J.</Author>
-<Author>Deal, C.D.</Author>
-<Author>Castric, P.</Author>
-</Authors>
-<Citation>Infect. Immun. 70, 2837-2845, 2002</Citation>
-<Title>Identification of the Pseudomonas aeruginosa 1244 pilin glycosylation site.</Title>
-<Xref>DOI:10.1128/IAI.70.6.2837-2845.2002</Xref>
-<Xref>PMID:12010970</Xref>
-<Note>beta-N-glycosidic linkage</Note>
-</ReferenceBlock>
-<Comment>See also RESID:AA0154, RESID:AA0208, RESID:AA0209, RESID:AA0210, RESID:AA0291, RESID:AA0296, RESID:AA0297, RESID:AA0397, RESID:AA0398, RESID:AA0400, RESID:AA0402, RESID:AA0404, and RESID:AA0406 for other O-glycosylated serines.</Comment>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>PSI-MOD:00834</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__o-linked (fucnac...) serine__s">CARBOHYD O-linked (FucNAc...) serine</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="carbohyd__o-linked (dhexnac...) serine__s">CARBOHYD O-linked (dHexNAc...) serine</Feature>
-<Note>this UniProt feature is used when the identity of the sugar has not been determined</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0422.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0422.PDB" />
-</Entry>
-<Entry id="AA0423">
-<Header>
-<Code>AA0423</Code>
-<Dates>
-<CreationDate>30-Jun-2006</CreationDate>
-<StrucRevDate>30-Jun-2006</StrucRevDate>
-<TextChngDate>30-Jun-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-acetyl-L-threonine</Name>
-<AlternateName>O-acetylthreonine</AlternateName>
-<AlternateName>threonine acetate ester</AlternateName>
-<SystematicName>(2S,3R)-3-(acetyloxy)-2-aminobutanoic acid</SystematicName>
-<Xref>CAS:17012-42-9</Xref>
-<Xref>PDBHET:TH5</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 9 N 1 O 3</Formula>
-<Weight type="chemical">143.14</Weight>
-<Weight type="physical">143.058243</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0017">
-<Formula>C 2 H 2 N 0 O 1</Formula>
-<Weight type="chemical">42.04</Weight>
-<Weight type="physical">42.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mukherjee, S.</Author>
-<Author>Keitany, G.</Author>
-<Author>Li, Y.</Author>
-<Author>Wang, Y.</Author>
-<Author>Ball, H.L.</Author>
-<Author>Goldsmith, E.J.</Author>
-<Author>Orth, K.</Author>
-</Authors>
-<Citation>Science 312, 1211-1214, 2006</Citation>
-<Title>Yersinia YopJ acetylates and inhibits kinase activation by blocking phosphorylation.</Title>
-<Xref>DOI:10.1126/science.1126867</Xref>
-<Xref>PMID:16728640</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Iqbal, A.</Author>
-<Author>Clifton, I.J.</Author>
-<Author>Bagonis, M.</Author>
-<Author>Kershaw, N.J.</Author>
-<Author>Domene, C.</Author>
-<Author>Claridge, T.D.</Author>
-<Author>Wharton, C.W.</Author>
-<Author>Schofield, C.J.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 131, 749-757, 2009</Citation>
-<Title>Anatomy of a simple acyl intermediate in enzyme catalysis: combined biophysical and modeling studies on ornithine acetyl transferase.</Title>
-<Xref>DOI:10.1021/ja807215u</Xref>
-<Xref>PMID:19105697</Xref>
-</ReferenceBlock>
-<Comment>O-acetylation of threonine in host kinases is catalyzed by yersinia toxin blocking the normal phosphorylation.</Comment>
-<SequenceCode>
-<SequenceSpec>T</SequenceSpec>
-<Xref>PSI-MOD:01171</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="mod_res__o-acetylthreonine__t">MOD_RES O-acetylthreonine</Feature>
-<Feature type="UniProt" key="act_site__o-acetylthreonine intermediate__t">ACT_SITE O-acetylthreonine intermediate</Feature>
-</Features>
-<Image src="/images/AA0423.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0423.PDB" />
-</Entry>
-<Entry id="AA0424">
-<Header>
-<Code>AA0424</Code>
-<Dates>
-<CreationDate>30-Jun-2006</CreationDate>
-<StrucRevDate>30-Jun-2006</StrucRevDate>
-<TextChngDate>30-Apr-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-alanyl-glycosylsphingolipidinositolethanolamine</Name>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 12 N 2 O 5 P 1 +</Formula>
-<Weight type="chemical">211.13 +</Weight>
-<Weight type="physical">211.048383 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0001">
-<Formula>C 2 H 6 N 1 O 3 P 1 +</Formula>
-<Weight type="chemical">123.05 +</Weight>
-<Weight type="physical">123.008530 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fontaine, T.</Author>
-<Author>Magnin, T.</Author>
-<Author>Melhert, A.</Author>
-<Author>Lamont, D.</Author>
-<Author>Latge, J.P.</Author>
-<Author>Ferguson, M.A.</Author>
-</Authors>
-<Citation>Glycobiology 13, 169-177, 2003</Citation>
-<Title>Structures of the glycosylphosphatidylinositol membrane anchors from Aspergillus fumigatus membrane proteins.</Title>
-<Xref>DOI:10.1093/glycob/cwg004</Xref>
-<Xref>PMID:12626404</Xref>
-</ReferenceBlock>
-<Comment>This modification is predicted for proteins with sequence characteristics for the GPI-like-anchor modification with sphingolipid, and with alanine at the cleavage and anchor attachment site.</Comment>
-<Comment>A representative glycan core structure is shown.</Comment>
-<Comment>Cleavage of a carboxyl terminal propeptide accompanies transamidation.</Comment>
-<SequenceCode>
-<SequenceSpec>A</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>PSI-MOD:01172</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>glycoprotein</Keyword>
-<Keyword>lipoprotein</Keyword>
-<Keyword>phosphoprotein</Keyword>
-<Keyword>sphingolipidinositol linkage</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__gpi-like-anchor amidated alanine__a">LIPID GPI-like-anchor amidated alanine</Feature>
-</Features>
-<Image src="/images/AA0424.GIF" alt="DUMMY.GIF" />
-</Entry>
-<Entry id="AA0425">
-<Header>
-<Code>AA0425</Code>
-<Dates>
-<CreationDate>30-Jun-2006</CreationDate>
-<StrucRevDate>30-Jun-2006</StrucRevDate>
-<TextChngDate>30-Apr-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-asparaginyl-glycosylsphingolipidinositolethanolamine</Name>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 13 N 3 O 6 P 1 +</Formula>
-<Weight type="chemical">254.16 +</Weight>
-<Weight type="physical">254.054197 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0003">
-<Formula>C 2 H 6 N 1 O 3 P 1 +</Formula>
-<Weight type="chemical">123.05 +</Weight>
-<Weight type="physical">123.008530 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Stevens, B.A.</Author>
-<Author>White, I.J.</Author>
-<Author>Hames, B.D.</Author>
-<Author>Hooper, N.M.</Author>
-</Authors>
-<Citation>Biochim. Biophys. Acta 1511, 317-329, 2001</Citation>
-<Title>The carboxyl terminus of Dictyostelium discoideum protein 1I encodes a functional glycosyl-phosphatidylinositol signal sequence.</Title>
-<Xref>DOI:10.1016/S0005-2736(01)00289-9</Xref>
-<Xref>PMID:11286975</Xref>
-<Note>evidence for asparagine at the cleavage and anchor attachment site; lipid resistance to phospholipase C indicates it does not contain phosphatidylinositol</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fontaine, T.</Author>
-<Author>Magnin, T.</Author>
-<Author>Melhert, A.</Author>
-<Author>Lamont, D.</Author>
-<Author>Latge, J.P.</Author>
-<Author>Ferguson, M.A.</Author>
-</Authors>
-<Citation>Glycobiology 13, 169-177, 2003</Citation>
-<Title>Structures of the glycosylphosphatidylinositol membrane anchors from Aspergillus fumigatus membrane proteins.</Title>
-<Xref>DOI:10.1093/glycob/cwg004</Xref>
-<Xref>PMID:12626404</Xref>
-</ReferenceBlock>
-<Comment>This modification is predicted for proteins with sequence characteristics for the GPI-like anchor modification with sphingolipid, and with asparagine at the cleavage and anchor attachment site.</Comment>
-<Comment>A representative glycan core structure is shown.</Comment>
-<Comment>Cleavage of a carboxyl terminal propeptide accompanies transamidation.</Comment>
-<SequenceCode>
-<SequenceSpec>N</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>PSI-MOD:01173</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>glycoprotein</Keyword>
-<Keyword>lipoprotein</Keyword>
-<Keyword>phosphoprotein</Keyword>
-<Keyword>sphingolipidinositol linkage</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__gpi-like-anchor amidated asparagine__n">LIPID GPI-like-anchor amidated asparagine</Feature>
-</Features>
-<Image src="/images/AA0425.GIF" alt="DUMMY.GIF" />
-</Entry>
-<Entry id="AA0426">
-<Header>
-<Code>AA0426</Code>
-<Dates>
-<CreationDate>30-Jun-2006</CreationDate>
-<StrucRevDate>30-Jun-2006</StrucRevDate>
-<TextChngDate>20-May-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-(15-deoxy-Delta12,14-prostaglandin J2-9-yl)-L-cysteine</Name>
-<AlternateName>(2R)-2-amino-3-([(5Z,9Xi,12E,14Z)-1-hydroxy-1,11-oxoprosta-5,12,14-trien-9-yl]sulfanyl)propanoic acid</AlternateName>
-<SystematicName>(5Z,9Xi,12E,14Z)-9-([(2R)-2-amino-3-carboxyethyl]sulfanyl)-11-oxoprosta-5,12,14-trien-1-oic acid</SystematicName>
-<Xref>CAS:60203-57-8</Xref>
-<Xref>ChEBI:27485</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 23 H 33 N 1 O 4 S 1</Formula>
-<Weight type="chemical">419.58</Weight>
-<Weight type="physical">419.213030</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 20 H 28 N 0 O 3 S 0</Formula>
-<Weight type="chemical">316.44</Weight>
-<Weight type="physical">316.203845</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Cernuda-Morollon, E.</Author>
-<Author>Pineda-Molina, E.</Author>
-<Author>Canada, F.J.</Author>
-<Author>Perez-Sala, D.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 276, 35530-35536, 2001</Citation>
-<Title>15-Deoxy-(Delta)12,14-prostaglandin J2 inhibition of NF-(kappa)B-DNA binding through covalent modification of the p50 subunit.</Title>
-<Xref>DOI:10.1074/jbc.M104518200</Xref>
-<Xref>PMID:11466314</Xref>
-<Note>mass spectrometric detection; directed mutation analysis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Oliva, J.L.</Author>
-<Author>Perez-Sala, D.</Author>
-<Author>Castrillo, A.</Author>
-<Author>Martinez, N.</Author>
-<Author>Canada, F.J.</Author>
-<Author>Bosca, L.</Author>
-<Author>Rojas, J.M.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 100, 4772-4777, 2003</Citation>
-<Title>The cyclopentenone 15-deoxy-(delta)12,14-prostaglandin J2 binds to and activates H-Ras.</Title>
-<Xref>DOI:10.1073/pnas.0735842100</Xref>
-<Xref>PMID:12684535</Xref>
-<Note>mass spectrometric detection; directed mutation analysis</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>PSI-MOD:01174</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lipoprotein</Keyword>
-<Keyword>prostaglandin</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__s-(15-deoxy-delta12,14-prostaglandin j2-9-yl)cysteine__c">LIPID S-(15-deoxy-Delta12,14-prostaglandin J2-9-yl)cysteine</Feature>
-</Features>
-<Image src="/images/AA0426.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0426.PDB" />
-</Entry>
-<Entry id="AA0427">
-<Header>
-<Code>AA0427</Code>
-<Dates>
-<CreationDate>30-Sep-2006</CreationDate>
-<StrucRevDate>30-Sep-2006</StrucRevDate>
-<TextChngDate>30-Sep-2008</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-phycourobilin-L-cysteine</Name>
-<AlternateName>18-ethenyl-3-[1-(2-amino-2-carboxyethylsulfanyl)ethyl]-2,3,15,16-dihydro-2,7,13,17-tetramethyl-1,19-dioxo-(21H,22H,24H)-bilin-8,12-dipropanoic acid</AlternateName>
-<AlternateName>phycourobilin cysteine adduct</AlternateName>
-<AlternateName>PUB</AlternateName>
-<SystematicName>(2S,3R,16R)-18-ethenyl-3-[(1R)-1-([(R)-2-amino-2-carboxyethyl]sulfanyl)ethyl]-8,12-bis(2-carboxyethyl)-2,7,13,17-tetramethyl-4,5,15,16-tetrahydrobiline-1,19(21H,22H,24H)-dione</SystematicName>
-<Xref>CAS:61932-71-6</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 36 H 43 N 5 O 7 S 1</Formula>
-<Weight type="chemical">689.83</Weight>
-<Weight type="physical">689.288320</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 33 H 38 N 4 O 6 S 0</Formula>
-<Weight type="chemical">586.69</Weight>
-<Weight type="physical">586.279135</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Nagy, J.O.</Author>
-<Author>Bishop, J.E.</Author>
-<Author>Klotz, A.V.</Author>
-<Author>Glazer, A.N.</Author>
-<Author>Rapoport, H.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 260, 4864-4868, 1985</Citation>
-<Title>Bilin attachment sites in the alpha, beta, and gamma subunits of R-phycoerythrin. Structural studies on singly and doubly linked phycourobilins.</Title>
-<Xref>PMID:3838747</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Moss, G.P.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 178, 277-328, 1988</Citation>
-<Title>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN). Nomenclature of tetrapyrroles. Recommendations 1986.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1988.tb14453.x</Xref>
-<Xref>PMID:3208761</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ong, L.J.</Author>
-<Author>Glazer, A.N.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 266, 9515-9527, 1991</Citation>
-<Title>Phycoerythrins of marine unicellular cyanobacteria. I. Bilin types and locations and energy transfer pathways in Synechococcus spp. phycoerythrins.</Title>
-<Xref>PMID:1903388</Xref>
-</ReferenceBlock>
-<Comment>There are additional chiral centers at C-3alpha, C-4, and C-16.</Comment>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>PSI-MOD:01175</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chromoprotein</Keyword>
-<Keyword>phycourobilin</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="binding__phycourobilin chromophore (covalent; via 1 link)__c">BINDING Phycourobilin chromophore (covalent; via 1 link)</Feature>
-</Features>
-<Image src="/images/AA0427.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0427.PDB" />
-</Entry>
-<Entry id="AA0428">
-<Header>
-<Code>AA0428</Code>
-<Dates>
-<CreationDate>30-Jun-2008</CreationDate>
-<StrucRevDate>30-Jun-2008</StrucRevDate>
-<TextChngDate>31-Mar-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-15,16-dihydrobiliverdin-L-cysteine</Name>
-<AlternateName>15,16-Dhbv</AlternateName>
-<AlternateName>15,16-dihydrobiliverdin cysteine adduct</AlternateName>
-<AlternateName>15,16-dihydrobiliverdin IXalpha</AlternateName>
-<AlternateName>18-ethenyl-8,12-bis(2-carboxyethyl)-3-(2-(cysteinyl-S)-ethyl)-2,7,13,17-tetramethylbiladiene-ab-1,19(16H,21H)-dione</AlternateName>
-<AlternateName>3'-cysteinyl-15,16-dihydrobiliverdin</AlternateName>
-<AlternateName>3alpha-cysteinyl-15,16-dihydrobiliverdin</AlternateName>
-<AlternateName>DBV</AlternateName>
-<SystematicName>(16R)-18-ethenyl-8,12-bis(2-carboxyethyl)-3-[(1R)-1-(((2R)-2-amino-2-carboxy)ethylsulfanyl)ethyl]-2,7,13,17-tetramethyl-15,16-dihydrobilin-1,19(21H,24H)-dione</SystematicName>
-<Xref>CAS:137429-14-2</Xref>
-<Xref>PDBHET:DBV</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 36 H 41 N 5 O 7 S 1</Formula>
-<Weight type="chemical">687.81</Weight>
-<Weight type="physical">687.272670</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 33 H 36 N 4 O 6 S 0</Formula>
-<Weight type="chemical">584.67</Weight>
-<Weight type="physical">584.263485</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Moss, G.P.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 178, 277-328, 1988</Citation>
-<Title>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN). Nomenclature of tetrapyrroles. Recommendations 1986.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1988.tb14453.x</Xref>
-<Xref>PMID:3208761</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wedemayer, G.J.</Author>
-<Author>Kidd, D.G.</Author>
-<Author>Wemmer, D.E.</Author>
-<Author>Glazer, A.N.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 267, 7315-7331, 1992</Citation>
-<Title>Phycobilins of cryptophycean algae. Occurrence of dihydrobiliverdin and mesobiliverdin in cryptomonad biliproteins.</Title>
-<Xref>PMID:1559975</Xref>
-<Note>a "cryptoviolin-like" chromophore is identified as 15,16-dihydrobiliverdin</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wilk, K.E.</Author>
-<Author>Harrop, S.J.</Author>
-<Author>Jankova, L.</Author>
-<Author>Edler, D.</Author>
-<Author>Keenan, G.</Author>
-<Author>Sharples, F.</Author>
-<Author>Hiller, R.G.</Author>
-<Author>Curmi, P.M.G.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 96, 8901-8906, 1999</Citation>
-<Title>Evolution of a light-harvesting protein by addition of new subunits and rearrangement of conserved elements: crystal structure of a cryptophyte phycoerythrin at 1.63-A resolution.</Title>
-<Xref>DOI:10.1073/pnas.96.16.8901</Xref>
-<Xref>PMID:10430868</Xref>
-<Note>X-ray diffraction, 1.63 angstroms; the initials of "P.M. Curmi" in the PubMed citation are corrected</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Harrop, S.J.</Author>
-<Author>Wilk, K.E.</Author>
-<Author>Hiller, R.G.</Author>
-<Author>Curmi, P.M.G.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, May 1999</Citation>
-<Description>Crystal structure of phycoerythrin 545 from the marine cryptophyte Rhodomonas CS24.</Description>
-<Xref>PDB:1QGW</Xref>
-<Note>X-ray diffraction, 1.63 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Doust, A.B.</Author>
-<Author>Marai, C.N.J.</Author>
-<Author>Harrop, S.J.</Author>
-<Author>Wilk, K.E.</Author>
-<Author>Curmi, P.M.G.</Author>
-<Author>Scholes, G.D.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 344, 135-153, 2004</Citation>
-<Title>Developing a structure-function model for the cryptophyte phycoerythrin 545 using ultrahigh resolution crystallography and ultrafast laser spectroscopy.</Title>
-<Xref>DOI:10.1016/j.jmb.2004.09.044</Xref>
-<Xref>PMID:15504407</Xref>
-<Note>X-ray diffraction, 1.63 angstroms; the initials of "C.N. Marai" and "P.M. Curmi" in the PubMed citation are corrected</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Doust, A.B.</Author>
-<Author>Marai, C.N.J.</Author>
-<Author>Harrop, S.J.</Author>
-<Author>Wilk, K.E.</Author>
-<Author>Curmi, P.M.G.</Author>
-<Author>Scholes, G.D.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, September 2004</Citation>
-<Description>High resolution crystal structure of phycoerythrin 545 from the marine cryptophyte Rhodomonas CS24.</Description>
-<Xref>PDB:1XF6</Xref>
-<Note>X-ray diffraction, 1.10 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Doust, A.B.</Author>
-<Author>Marai, C.N.J.</Author>
-<Author>Harrop, S.J.</Author>
-<Author>Wilk, K.E.</Author>
-<Author>Curmi, P.M.G.</Author>
-<Author>Scholes, G.D.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, September 2004</Citation>
-<Description>High resolution crystal structure of phycoerythrin 545 from the marine cryptophyte Rhodomonas CS24.</Description>
-<Xref>PDB:1XG0</Xref>
-<Note>X-ray diffraction, 0.97 angstroms</Note>
-</ReferenceBlock>
-<Comment>15,16-dihydrobiliverdin transmits violet.</Comment>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>PSI-MOD:01142</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chromoprotein</Keyword>
-<Keyword>dihydrobiliverdin</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="binding__15,16-dihydrobiliverdin (covalent; via 1 link)__c">BINDING 15,16-dihydrobiliverdin (covalent; via 1 link)</Feature>
-</Features>
-<Image src="/images/AA0428.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0428.PDB" />
-</Entry>
-<Entry id="AA0429">
-<Header>
-<Code>AA0429</Code>
-<Dates>
-<CreationDate>30-Jun-2008</CreationDate>
-<StrucRevDate>30-Jun-2008</StrucRevDate>
-<TextChngDate>30-Jan-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>15,16-dihydrobiliverdin-bis-L-cysteine</Name>
-<AlternateName>15,16-Dhbv</AlternateName>
-<AlternateName>15,16-dihydrobiliverdin cysteine adduct</AlternateName>
-<AlternateName>15,16-dihydrobiliverdin IXalpha</AlternateName>
-<AlternateName>3'',18'-biscysteinyl-15,16-dihydrobiliverdin</AlternateName>
-<AlternateName>3beta,18alpha-biscysteinyl-15,16-dihydrobiliverdin</AlternateName>
-<AlternateName>8,12-bis(2-carboxyethyl)-3-(2-(cysteinyl-S)-ethyl)-18-(1-(cysteinyl-S)-ethyl)-2,7,13,17-tetramethylbiladiene-ab-1,19(16H,21H)-dione</AlternateName>
-<AlternateName>DBV</AlternateName>
-<SystematicName>(16R)-8,12-bis(2-carboxyethyl)-3-[2-(((2R)-2-amino-2-carboxy)ethylsulfanyl)ethyl]-18-[(1Xi)-1-(((2R)-2-amino-2-carboxy)ethylsulfanyl)ethyl]-2,7,13,17-tetramethyl-15,16-dihydrobilin-1,19(21H,24H)-dione</SystematicName>
-<Xref>CAS:137429-14-2</Xref>
-<Xref>PDBHET:DBV</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 39 H 46 N 6 O 8 S 2</Formula>
-<Weight type="chemical">790.95</Weight>
-<Weight type="physical">790.281854</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005">
-<Formula>C 33 H 36 N 4 O 6 S 0</Formula>
-<Weight type="chemical">584.67</Weight>
-<Weight type="physical">584.263485</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Moss, G.P.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 178, 277-328, 1988</Citation>
-<Title>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN). Nomenclature of tetrapyrroles. Recommendations 1986.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1988.tb14453.x</Xref>
-<Xref>PMID:3208761</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sidler, W.</Author>
-<Author>Nutt, H.</Author>
-<Author>Kumpf, B.</Author>
-<Author>Frank, G.</Author>
-<Author>Suter, F.</Author>
-<Author>Brenzel, A.</Author>
-<Author>Wehrmeyer, W.</Author>
-<Author>Zuber, H.</Author>
-</Authors>
-<Citation>Biol. Chem. Hoppe-Seyler 371, 537-547, 1990</Citation>
-<Title>The complete amino-acid sequence and the phylogenetic origin of phycocyanin-645 from the cryptophytan alga Chroomonas sp.</Title>
-<Xref>PMID:2222853</Xref>
-<Note>a double-linked, "cryptoviolin-like" chromophore is detected</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wedemayer, G.J.</Author>
-<Author>Kidd, D.G.</Author>
-<Author>Wemmer, D.E.</Author>
-<Author>Glazer, A.N.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 267, 7315-7331, 1992</Citation>
-<Title>Phycobilins of cryptophycean algae. Occurrence of dihydrobiliverdin and mesobiliverdin in cryptomonad biliproteins.</Title>
-<Xref>PMID:1559975</Xref>
-<Note>the "cryptoviolin-like" chromophore is identified as 15,16-dihydrobiliverdin</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wemmer, D.E.</Author>
-<Author>Wedemayer, G.J.</Author>
-<Author>Glazer, A.N.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 268, 1658-1669, 1993</Citation>
-<Title>Phycobilins of cryptophycean algae. Novel linkage of dihydrobiliverdin in a phycoerythrin 555 and a phycocyanin 645.</Title>
-<Xref>PMID:8420941</Xref>
-<Note>by mass spectrometric, (1)H-NMR, and (13)C-NMR analysis, the 15,16-dihydrobiliverdin is determined to be attached to Cys-50 by C18', and to Cys-61 by C33''</Note>
-</ReferenceBlock>
-<Comment>This bilin transmits violet.</Comment>
-<Comment>The stereochemistry for the 18' chiral center has not been resolved.</Comment>
-<SequenceCode>
-<SequenceSpec>C, C</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:01143</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chromoprotein</Keyword>
-<Keyword>dihydrobiliverdin</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="binding__15,16-dihydrobiliverdin (covalent; via 2 links)__c__c">BINDING  15,16-dihydrobiliverdin (covalent; via 2 links)</Feature>
-</Features>
-<Image src="/images/AA0429.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0429.PDB" />
-</Entry>
-<Entry id="AA0430">
-<Header>
-<Code>AA0430</Code>
-<Dates>
-<CreationDate>30-Sep-2006</CreationDate>
-<StrucRevDate>30-Sep-2006</StrucRevDate>
-<TextChngDate>30-Jun-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-dehydrolysinonorleucine</Name>
-<AlternateName>6-(N6-L-didehydrolysino)-L-norleucine</AlternateName>
-<AlternateName>dehydrolysinorleucine [misspelling]</AlternateName>
-<AlternateName>dehydrolysylnorleucine</AlternateName>
-<AlternateName>didehydrolysinonorleucine</AlternateName>
-<AlternateName>N6-[(5S)-5-amino-5-carboxypentylidene]-L-lysine</AlternateName>
-<SystematicName>(2S)-2-amino-6-([(5S)-5-amino-5-carboxypentylidene]amino)hexanoic acid</SystematicName>
-<Xref>CAS:31504-14-0</Xref>
-<Xref>ChEBI:64748</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 12 H 19 N 3 O 2</Formula>
-<Weight type="chemical">237.30</Weight>
-<Weight type="physical">237.147727</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012 AA0012">
-<Formula>C 0 H -5 N -1 O 0</Formula>
-<Weight type="chemical">-19.05</Weight>
-<Weight type="physical">-19.042199</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Franzblau, C.</Author>
-<Author>Sinex, F.M.</Author>
-<Author>Faris, B.</Author>
-<Author>Lampidis, R.</Author>
-</Authors>
-<Citation>Biochem. Biophys. Res. Commun. 21, 575-581, 1965</Citation>
-<Title>Identification of a new crosslinking amino acid in elastin.</Title>
-<Xref>PMID:5879466</Xref>
-<Note>isolation of reduced form; chemical characterization and naming of lysinonorleucine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Franzblau, C.</Author>
-<Author>Faris, B.</Author>
-<Author>Papaioannou, R.</Author>
-</Authors>
-<Citation>Biochemistry 8, 2833-2837, 1969</Citation>
-<Title>Lysinonorleucine. A new amino acid from hydrolysates of elastin.</Title>
-<Xref>PMID:5817620</Xref>
-<Note>mass spectrometric and chemical characterization of the reduced form; stereochemical determination</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lent, R.</Author>
-<Author>Franzblau, C.</Author>
-</Authors>
-<Citation>Biochem. Biophys. Res. Commun. 26, 43-50, 1967</Citation>
-<Title>Studies on the reduction of bovine elastin: evidence for the presence of Delta-6,7-dehydrolysinonorleucine.</Title>
-<Xref>PMID:6030254</Xref>
-<Note>observation of the aldimine form</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bailey, A.J.</Author>
-<Author>Peach, C.M.</Author>
-</Authors>
-<Citation>Biochem. J. 121, 257-259, 1971</Citation>
-<Title>The chemistry of the collagen cross-links. The absence of reduction of dehydrolysinonorleucine and dehydrohydroxylysinonorleucine in vivo.</Title>
-<Xref>PMID:5117030</Xref>
-<Note>the non-reduced aldimine form is the predominant form in collagen, and in insoluble collagens there is less hydroxylation; the predominant form in elastin is the reduced lysinonorleucine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Duff, A.P.</Author>
-<Author>Cohen, A.E.</Author>
-<Author>Ellis, P.J.</Author>
-<Author>Hilmer, K.</Author>
-<Author>Langley, D.B.</Author>
-<Author>Dooley, D.M.</Author>
-<Author>Freeman, H.C.</Author>
-<Author>Guss, J.M.</Author>
-</Authors>
-<Citation>Acta Crystallogr. D Biol. Crystallogr. 62, 1073-1084, 2006</Citation>
-<Title>The 1.23 A structure of Pichia pastoris lysyl oxidase reveals a lysine-lysine cross-link.</Title>
-<Xref>DOI:10.1107/S0907444906026333</Xref>
-<Xref>PMID:16929109</Xref>
-<Note>X-ray diffraction, 1.23 angstroms; the authors estimate that 35% of the protein molecules in the crystal contain this cross-link</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Duff, A.P.</Author>
-<Author>Cohen, A.E.</Author>
-<Author>Ellis, P.J.</Author>
-<Author>Guss, J.M.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, September 2004</Citation>
-<Description>PPLO at 1.23 angstroms.</Description>
-<Xref>PDB:1W7C</Xref>
-<Note>X-ray diffraction, 1.23 angstroms</Note>
-</ReferenceBlock>
-<Comment>Although it should not be possible to distinguish dehydrolysinonorleucine from lysinonorleucine in the X-ray structure, the cross-link was probably not reduced.</Comment>
-<Comment>After the oxidation of a lysine to allysine (see RESID:AA0121), this cross-link forms spontaneously with a Schiff-base reaction. In this aleatoric modification two peptide chains may be crosslinked with the peptides contributing a lysine in either biosynthetic position.</Comment>
-<Comment>The lysines forming the cross-link may also be hydroxylated and glycosylated (see RESID:AA0028 and RESID:AA0153).</Comment>
-<GeneratingEnzyme>
-<EnzymeName>lysyl oxidase (EC 1.4.3.13)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>K, K</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Condition>incidental to RESID:AA0028</Condition>
-<Condition>incidental to RESID:AA0147</Condition>
-<Condition>secondary to RESID:AA0121</Condition>
-<Xref>PSI-MOD:01176</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>aleatoric crosslink</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__dehydrolysinonorleucine (lys-lys)__k__k">CROSSLNK Dehydrolysinonorleucine (Lys-Lys)</Feature>
-</Features>
-<Image src="/images/AA0430.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0430.PDB" />
-</Entry>
-<Entry id="AA0431">
-<Header>
-<Code>AA0431</Code>
-<Dates>
-<CreationDate>31-Dec-2006</CreationDate>
-<StrucRevDate>31-Dec-2006</StrucRevDate>
-<TextChngDate>29-Jan-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>1'-(1,2,3-trihydroxyprop-2-yl)-L-histidine</Name>
-<AlternateName>1-[1,2-dihydroxy-1-(hydroxymethyl)ethyl]-L-histidine</AlternateName>
-<AlternateName>N(epsilon)-histidine dihydroxyacetone adduct</AlternateName>
-<AlternateName>N(tau)-(1,2,3-trihydroxypropan-2-yl)histidine</AlternateName>
-<AlternateName>tele-(1,2,3-trihydroxypropan-2-yl)histidine</AlternateName>
-<SystematicName>(S)-2-amino-3-[1-(1,2,3-trihydroxypropan-2-yl)-1H-imidazol-4-yl]propanoic acid</SystematicName>
-<Xref>PDBHET:HIQ</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 13 N 3 O 4</Formula>
-<Weight type="chemical">227.22</Weight>
-<Weight type="physical">227.090606</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0009">
-<Formula>C 3 H 6 N 0 O 3</Formula>
-<Weight type="chemical">90.08</Weight>
-<Weight type="physical">90.031694</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Christen, S.</Author>
-<Author>Srinivas, A.</Author>
-<Author>Baehler, P.</Author>
-<Author>Zeller, A.</Author>
-<Author>Pridmore, D.</Author>
-<Author>Bieniossek, C.</Author>
-<Author>Baumann, U.</Author>
-<Author>Erni, B.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 281, 23129-23137, 2006</Citation>
-<Title>Regulation of the Dha operon of Lactococcus lactis: a deviation from the rule followed by the Tetr family of transcription regulators.</Title>
-<Xref>DOI:10.1074/jbc.M603486200</Xref>
-<Xref>PMID:16760471</Xref>
-<Note>X-ray diffraction, 1.96 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Srinivas, A.</Author>
-<Author>Christen, S.</Author>
-<Author>Baumann, U.</Author>
-<Author>Erni, B.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, May 2006</Citation>
-<Description>Dihydroxyacetone kinase operon co-activator Dha-dhaQ.</Description>
-<Xref>PDB:2IU4</Xref>
-<Note>X-ray diffraction, 1.96 angstroms</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>H</SequenceSpec>
-<Xref>PSI-MOD:01177</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="binding__tele-(1,2,3-trihydroxypropan-2-yl)histidine__h">MOD_RES Tele-(1,2,3-trihydroxypropan-2-yl)histidine</Feature>
-</Features>
-<Image src="/images/AA0431.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0431.PDB" />
-</Entry>
-<Entry id="AA0432">
-<Header>
-<Code>AA0432</Code>
-<Dates>
-<CreationDate>30-Sep-2007</CreationDate>
-<StrucRevDate>30-Sep-2007</StrucRevDate>
-<TextChngDate>30-Jun-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-(aspart-4-yloxy) thiocarbonate</Name>
-<AlternateName>4-aspartyloxysulfanylcarbonate</AlternateName>
-<AlternateName>O-carboxysulfanyl-4-oxo-L-homoserine</AlternateName>
-<SystematicName>(2S)-2-amino-4-(carboxysulfanyl)oxy-4-oxobutanoic acid</SystematicName>
-<Xref>PDBHET:OHS</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 5 N 1 O 5 S 1</Formula>
-<Weight type="chemical">191.16</Weight>
-<Weight type="physical">190.988843</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0004">
-<Formula>C 1 H 0 N 0 O 2 S 1</Formula>
-<Weight type="chemical">76.07</Weight>
-<Weight type="physical">75.961900</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Shimon, L.J.</Author>
-<Author>Goihberg, E.</Author>
-<Author>Peretz, M.</Author>
-<Author>Burstein, Y.</Author>
-<Author>Frolow, F.</Author>
-</Authors>
-<Citation>Acta Crystallogr. D Biol. Crystallogr. 62, 541-547, 2006</Citation>
-<Title>Structure of alcohol dehydrogenase from Entamoeba histolytica.</Title>
-<Xref>DOI:10.1107/S0907444906009292</Xref>
-<Xref>PMID:16627948</Xref>
-<Note>X-ray diffraction, 1.8 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Shimon, L.J.</Author>
-<Author>Peretz, M.</Author>
-<Author>Goihberg, E.</Author>
-<Author>Burstein, Y.</Author>
-<Author>Frolow, F.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, December 2004</Citation>
-<Description>Alcohol dehydrogenase from Entamoeba histolotica in complex with cacodylate.</Description>
-<Xref>PDB:1Y9A</Xref>
-<Note>X-ray diffraction, 1.81 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Goihberg, E.</Author>
-<Author>Dym, O.</Author>
-<Author>Tel-Or, S.</Author>
-<Author>Shimon, L.</Author>
-<Author>Frolow, F.</Author>
-<Author>Peretz, M.</Author>
-<Author>Burstein, Y.</Author>
-</Authors>
-<Citation>Proteins 72, 711-719, 2008</Citation>
-<Title>Thermal stabilization of the protozoan Entamoeba histolytica alcohol dehydrogenase by a single proline substitution.</Title>
-<Xref>DOI:10.1002/prot.21946</Xref>
-<Xref>PMID:18260103</Xref>
-<Note>X-ray diffraction, 1.77 angstroms; the modification is not mentioned</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Frolow, F.</Author>
-<Author>Shimon, L.</Author>
-<Author>Burstein, Y.</Author>
-<Author>Goihberg, E.</Author>
-<Author>Peretz, M.</Author>
-<Author>Dym, O.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, February 2007</Citation>
-<Description>D275P mutant of alcohol dehydrogenase from protozoa Entamoeba histolytica.</Description>
-<Xref>PDB:2OUI</Xref>
-<Note>X-ray diffraction, 1.77 angstroms; the modification is not presented in the model</Note>
-</ReferenceBlock>
-<Comment>This modification was originally observed in the enzyme expressed in Escherichia coli. It was not chemically confirmed or characterized. It did not appear in a later model at higher resolution by the same group.</Comment>
-<SequenceCode>
-<SequenceSpec>D</SequenceSpec>
-<Xref>PSI-MOD:01178</Xref>
-</SequenceCode>
-<Source>deprecated</Source>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this dubious modification is not currently annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0432.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0432.PDB" />
-</Entry>
-<Entry id="AA0433">
-<Header>
-<Code>AA0433</Code>
-<Dates>
-<CreationDate>30-Sep-2007</CreationDate>
-<StrucRevDate>30-Sep-2007</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N,N-dimethyl-L-alanine</Name>
-<AlternateName>(S)-1-carboxy-N,N-dimethylaminoethane</AlternateName>
-<AlternateName>N,N-dimethylalanine</AlternateName>
-<SystematicName>(S)-2-(dimethylamino)propanoic acid</SystematicName>
-<Xref>CAS:2812-31-9</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 10 N 1 O 1</Formula>
-<Weight type="chemical">100.14</Weight>
-<Weight type="physical">100.076239</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0001">
-<Formula>C 2 H 4 N 0 O 0</Formula>
-<Weight type="chemical">28.05</Weight>
-<Weight type="physical">28.031300</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Alix, J.H.</Author>
-<Author>Hayes, D.</Author>
-<Author>Lontie, J.F.</Author>
-<Author>Colson, C.</Author>
-<Author>Glatigny, A.</Author>
-<Author>Lederer, F.</Author>
-</Authors>
-<Citation>Biochimie 61, 671-679, 1979</Citation>
-<Title>Methylated amino acids in ribosomal proteins from Escherichia coli treated with ethionine and from a mutant lacking methylation of protein L11.</Title>
-<Xref>DOI:10.1016/S0300-9084(79)80165-0</Xref>
-<Xref>PMID:387091</Xref>
-<Note>N,N-dimethylalanine identified in ribosomal protein L11 after ethionine treatment</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Minami, Y.</Author>
-<Author>Yoshida, K.</Author>
-<Author>Azuma, R.</Author>
-<Author>Urakawa, A.</Author>
-<Author>Kawauchi, T.</Author>
-<Author>Otani, T.</Author>
-<Author>Komiyama, K.</Author>
-<Author>Omura, S.</Author>
-</Authors>
-<Citation>Tetrahedron Lett. 35, 8001-8004, 1994</Citation>
-<Title>Structure of cypemycin, a new peptide antibiotic.</Title>
-<Xref>DOI:10.1016/0040-4039(94)80033-2</Xref>
-<Note>mass spectrometric, (1)H-NMR, and (13)C-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bergmüller, E.</Author>
-<Author>Gehrig, P.M.</Author>
-<Author>Gruissem, W.</Author>
-</Authors>
-<Citation>J. Proteome Res. 6, 3655-3668, 2007</Citation>
-<Title>Characterization of Post-Translational Modifications of Histone H2B-Variants Isolated from Arabidopsis thaliana.</Title>
-<Xref>DOI:10.1021/pr0702159</Xref>
-<Xref>PMID:17691833</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Claesen, J.</Author>
-<Author>Bibb, M.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 107, 16297-16302, 2010</Citation>
-<Title>Genome mining and genetic analysis of cypemycin biosynthesis reveal an unusual class of posttranslationally modified peptides.</Title>
-<Xref>DOI:10.1073/pnas.1008608107</Xref>
-<Xref>PMID:20805503</Xref>
-<Note>gene sequence for the encoded peptide</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>ribosomal protein L11 methyltransferase prmA (EC 2.1.1.-)</EnzymeName>
-<EnzymeName>N-terminal RCC1 methyltransferase</EnzymeName>
-<EnzymeName>protein N-terminal methyltransferase</EnzymeName>
-<EnzymeName>S-adenosyl-L-methionine:N-terminal-(A,P,S)PK-[protein] methyltransferase (EC 2.1.1.244)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>A</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0018011</Xref>
-<Xref>PSI-MOD:01179</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-<Keyword>methylated amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n,n-dimethylalanine__a">MOD_RES N,N-dimethylalanine</Feature>
-</Features>
-<Image src="/images/AA0433.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0433.PDB" />
-</Entry>
-<Entry id="AA0434">
-<Header>
-<Code>AA0434</Code>
-<Dates>
-<CreationDate>30-Sep-2007</CreationDate>
-<StrucRevDate>30-Sep-2007</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>2-hydroxyglycine</Name>
-<AlternateName>alpha-hydroxyglycine</AlternateName>
-<AlternateName>aminohydroxyacetic acid</AlternateName>
-<SystematicName>amino(hydroxy)acetic acid</SystematicName>
-<Xref>CAS:4746-62-7</Xref>
-<Xref>ChEBI:38048</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 2 H 3 N 1 O 2</Formula>
-<Weight type="chemical">73.05</Weight>
-<Weight type="physical">73.016378</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0008">
-<Formula>C 0 H 0 N 0 O 1</Formula>
-<Weight type="chemical">16.00</Weight>
-<Weight type="physical">15.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Young, S.D.</Author>
-<Author>Tamburini, P.P.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 111, 1933-1934, 1989</Citation>
-<Title>Enzymatic peptidyl alpha-amidation proceeds through formation of an alpha-hydroxyglycine intermediate.</Title>
-<Xref>DOI:10.1021/ja00187a088</Xref>
-<Note>demonstration that the first step of peptide amide formation is the monooxidation of peptidylglycine to 2-hydroxyglycine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hoefnagel, A.J.</Author>
-<Author>van Bekkum, H.</Author>
-<Author>Peters, J.A.</Author>
-</Authors>
-<Citation>J. Org. Chem. 57, 3916-3921, 1992</Citation>
-<Title>The reaction of glyoxylic acid with ammonia revisited.</Title>
-<Xref>DOI:10.1021/jo00040a035</Xref>
-<Note>synthesis of hydoxyglycine peptides and observation of their decomposition</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hagelin, G.</Author>
-</Authors>
-<Citation>J. Mass Spectrom. 40, 1287-1299, 2005</Citation>
-<Title>Structure investigation of Maltacine D1a, D1b and D1c-cyclic peptide lactones of the Maltacine complex from Bacillus subtilis.</Title>
-<Xref>DOI:10.1002/jms.897</Xref>
-<Xref>PMID:16178056</Xref>
-<Note>reported mass spectrometric detection of hydroxyglycine in an antibiotic peptide</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Asara, J.M.</Author>
-<Author>Schweitzer, M.H.</Author>
-<Author>Freimark, L.M.</Author>
-<Author>Phillips, M.</Author>
-<Author>Cantley, L.C.</Author>
-</Authors>
-<Citation>Science 316, 280-285, 2007</Citation>
-<Title>Protein sequences from mastodon and Tyrannosaurus rex revealed by mass spectrometry.</Title>
-<Xref>DOI:10.1126/science.1137614</Xref>
-<Xref>PMID:17431180</Xref>
-<Note>reported mass spectrometric detection of hydroxyglycine in archaeological samples of collagen peptides</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Asara, J.M.</Author>
-<Author>Garavelli, J.S.</Author>
-<Author>Slatter, D.A.</Author>
-<Author>Schweitzer, M.H.</Author>
-<Author>Freimark, L.M.</Author>
-<Author>Phillips, M.</Author>
-<Author>Cantley, L.C.</Author>
-</Authors>
-<Citation>Science 317, 1324-1325, 2007</Citation>
-<Title>Interpreting Sequences from Mastodon and T. rex.</Title>
-<Xref>DOI:10.1126/science.317.5843.1324</Xref>
-<Xref>PMID:17823333</Xref>
-<Note>reinterpretation of mass spectrograms of collagen peptides</Note>
-</ReferenceBlock>
-<Comment>The S form, produced by peptidylglycine alpha-hydroxylating monooxygenase, is shown.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptidylglycine monooxygenase (EC 1.14.17.3)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>G</SequenceSpec>
-<Xref>PSI-MOD:01180</Xref>
-</SequenceCode>
-<Source>deprecated</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this dubious modification is not currently annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0434.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0434.PDB" />
-</Entry>
-<Entry id="AA0435">
-<Header>
-<Code>AA0435</Code>
-<Dates>
-<CreationDate>30-Sep-2007</CreationDate>
-<StrucRevDate>30-Sep-2007</StrucRevDate>
-<TextChngDate>30-Sep-2008</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-aspartic acid 4-methyl ester</Name>
-<AlternateName>2-aminobutanedioic acid 4-methyl ester</AlternateName>
-<AlternateName>4-methyl L-2-aminosuccinic acid</AlternateName>
-<AlternateName>4-methyl L-aspartate</AlternateName>
-<AlternateName>4-methyl L-hydrogen aspartate</AlternateName>
-<AlternateName>aspartic acid 4-methyl ester</AlternateName>
-<AlternateName>aspartic acid beta-methyl ester</AlternateName>
-<SystematicName>(2S)-2-amino-4-methoxy-4-oxobutanoic acid</SystematicName>
-<Xref>CAS:16856-13-6</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 7 N 1 O 3</Formula>
-<Weight type="chemical">129.12</Weight>
-<Weight type="physical">129.042593</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0004">
-<Formula>C 1 H 2 N 0 O 0</Formula>
-<Weight type="chemical">14.03</Weight>
-<Weight type="physical">14.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lowenson, J.D.</Author>
-<Author>Clarke, S.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 267, 5985-5995, 1992</Citation>
-<Title>Recognition of D-aspartyl residues in polypeptides by the erythrocyte L-isoaspartyl/D-aspartyl protein methyltransferase. Implications for the repair hypothesis.</Title>
-<Xref>PMID:1556110</Xref>
-<Note>repair enzyme acts on L-isoaspartyl and D-aspartyl peptides</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Haebel, S.</Author>
-<Author>Albrecht, T.</Author>
-<Author>Sparbier, K.</Author>
-<Author>Walden, P.</Author>
-<Author>Körner, R.</Author>
-<Author>Steup, M.</Author>
-</Authors>
-<Citation>Electrophoresis 19, 679-686, 1998</Citation>
-<Title>Electrophoresis-related protein modification: alkylation of carboxy residues revealed by mass spectrometry.</Title>
-<Xref>DOI:10.1002/elps.1150190513</Xref>
-<Xref>PMID:9629898</Xref>
-<Note>artifactual production of aspartyl and glutamyl methyl esters</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hoelz, D.J.</Author>
-<Author>Arnold, R.J.</Author>
-<Author>Dobrolecki, L.E.</Author>
-<Author>Abdel-Aziz, W.</Author>
-<Author>Loehrer, A.P.</Author>
-<Author>Novotny, M.V.</Author>
-<Author>Schnaper, L.</Author>
-<Author>Hickey, R.J.</Author>
-<Author>Malkas, L.H.</Author>
-</Authors>
-<Citation>Proteomics 6, 4808-4816, 2006</Citation>
-<Title>The discovery of labile methyl esters on proliferating cell nuclear antigen by MS/MS.</Title>
-<Xref>DOI:10.1002/pmic.200600142</Xref>
-<Xref>PMID:16888766</Xref>
-<Note>aspartate methyl ester is reported, but not located, resolved as either D- or L-aspartate, or otherwise chemically characterized</Note>
-</ReferenceBlock>
-<Comment>An enzyme acting to form the methyl ester of L-aspartyl peptides might interfere with the D-aspartyl peptide repair mechanism.</Comment>
-<SequenceCode>
-<SequenceSpec>D</SequenceSpec>
-<Xref>PSI-MOD:01181</Xref>
-</SequenceCode>
-<Source>deprecated</Source>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this dubious modification is not currently annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0435.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0435.PDB" />
-</Entry>
-<Entry id="AA0436">
-<Header>
-<Code>AA0436</Code>
-<Dates>
-<CreationDate>09-Nov-2007</CreationDate>
-<StrucRevDate>09-Nov-2007</StrucRevDate>
-<TextChngDate>30-Apr-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>6-(S-L-cysteinyl)-8alpha-(N3'-L-histidino)-FAD</Name>
-<AlternateName>6-(S-cysteinyl)-8alpha-(N(delta1)-histidyl)-FAD</AlternateName>
-<AlternateName>6-(S-cysteinyl)-8alpha-(N(pi)-histidyl)-FAD</AlternateName>
-<AlternateName>6-(S-cysteinyl)-8alpha-(N3'-histidyl)-FAD</AlternateName>
-<AlternateName>6-(S-cysteinyl)-8alpha-(pros-histidyl)-FAD</AlternateName>
-<SystematicName>6-((R)-2-amino-2-carboxyethyl)sulfanyl-8alpha-[4-((S)-2-amino-2-carboxyethyl)imidazol-3-yl]-riboflavin 5'-(trihydrogen diphosphate) 5'-&gt;5'-ester with adenosine</SystematicName>
-<Xref>PDBHET:FAD</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 36 H 41 N 13 O 17 P 2 S 1</Formula>
-<Weight type="chemical">1021.81</Weight>
-<Weight type="physical">1021.193931</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0009">
-<Formula>C 27 H 29 N 9 O 15 P 2 S 0</Formula>
-<Weight type="chemical">781.52</Weight>
-<Weight type="physical">781.125835</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Huang, C.H.</Author>
-<Author>Lai, W.L.</Author>
-<Author>Lee, M.H.</Author>
-<Author>Chen, C.J.</Author>
-<Author>Vasella, A.</Author>
-<Author>Tsai, Y.C.</Author>
-<Author>Liaw, S.H.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 280, 38831-38838, 2005</Citation>
-<Title>Crystal structure of glucooligosaccharide oxidase from Acremonium strictum: a novel flavinylation of 6-S-cysteinyl, 8alpha-N1-histidyl FAD.</Title>
-<Xref>DOI:10.1074/jbc.M506078200</Xref>
-<Xref>PMID:16154992</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Huang, C.-H.</Author>
-<Author>Lai, W.-L.</Author>
-<Author>Vasella, A.</Author>
-<Author>Tsai, Y.-C.</Author>
-<Author>Liaw, S.-H.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, September 2005</Citation>
-<Description>Crystal structure of glucooligosaccharide oxidase from Acremonium strictum: a novel flavinylation of 6-S-cysteinyl, 8alpha-N1-histidyl FAD.</Description>
-<Xref>PDB:2AXR</Xref>
-<Note>X-ray diffraction, 1.98 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Alexeev, I.</Author>
-<Author>Sultana, A.</Author>
-<Author>Mäntsälä, P.</Author>
-<Author>Niemi, J.</Author>
-<Author>Schneider, G.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 104, 6170-6175, 2007</Citation>
-<Title>Aclacinomycin oxidoreductase (AknOx) from the biosynthetic pathway of the antibiotic aclacinomycin is an unusual flavoenzyme with a dual active site.</Title>
-<Xref>DOI:10.1073/pnas.0700579104</Xref>
-<Xref>PMID:17395717</Xref>
-<Note>X-ray diffraction, 1.65 angstroms</Note>
-</ReferenceBlock>
-<Comment>The keyword "phosphoprotein" is not used with flavin modifications linked through the flavin.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C, H</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:01182</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>*phosphoprotein</Keyword>
-<Keyword>FAD</Keyword>
-<Keyword>flavoprotein</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="binding__fad (covalent; via 2 links, pros nitrogen)__h">BINDING FAD (covalent; via 2 links, pros nitrogen)</Feature>
-<Feature type="UniProt" key="binding__fad (covalent; via 2 links)__c">BINDING FAD (covalent; via 2 links)</Feature>
-</Features>
-<Image src="/images/AA0436.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0436.PDB" />
-</Entry>
-<Entry id="AA0437">
-<Header>
-<Code>AA0437</Code>
-<Dates>
-<CreationDate>09-Nov-2007</CreationDate>
-<StrucRevDate>09-Nov-2007</StrucRevDate>
-<TextChngDate>30-Jun-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-selenocystine</Name>
-<AlternateName>3,3'-diselenobis(2-aminopropanoic acid)</AlternateName>
-<AlternateName>3,3'-diselenobisalanine</AlternateName>
-<AlternateName>3,3'-diselenodialanine</AlternateName>
-<AlternateName>beta,beta'-diamino-beta,beta'-dicarboxydiethyldiselenide</AlternateName>
-<AlternateName>beta,beta'-diselenodialanine</AlternateName>
-<AlternateName>bis(alpha-aminopropionic acid)-beta-diselenide</AlternateName>
-<AlternateName>bis(beta-amino-beta-carboxyethyl)diselenide</AlternateName>
-<AlternateName>diselenocysteine</AlternateName>
-<AlternateName>selenium cystine</AlternateName>
-<SystematicName>(R,R)-3,3'-diselane-1,2-diylbis(2-aminopropanoic acid)</SystematicName>
-<Xref>CAS:1464-43-3</Xref>
-<Xref>ChEBI:28553</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 8 N 2 O 2 Se 2</Formula>
-<Weight type="chemical">298.08</Weight>
-<Weight type="physical">299.891620</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0022 AA0022" label="SEC2">
-<Formula>C 0 H -2 N 0 O 0 Se 0</Formula>
-<Weight type="chemical">-2.02</Weight>
-<Weight type="physical">-2.015650</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0005 AA0005" label="CYS2">
-<Formula>C 0 H -2 N 0 O 0 S -2 Se 2</Formula>
-<Weight type="chemical">91.81</Weight>
-<Weight type="physical">93.873250</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Huber, R.E.</Author>
-<Author>Criddle, R.S.</Author>
-</Authors>
-<Citation>Arch. Biochem. Biophys. 122, 164-173, 1967</Citation>
-<Title>Comparison of the chemical properties of selenocysteine and selenocystine with their sulfur analogs.</Title>
-<Xref>DOI:10.1016/0003-9861(67)90136-1</Xref>
-<Xref>PMID:6076213</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Shchedrina, V.A.</Author>
-<Author>Novoselov, S.V.</Author>
-<Author>Malinouski, M.Y.</Author>
-<Author>Gladyshev, V.N.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 104, 13919-13924, 2007</Citation>
-<Title>Identification and characterization of a selenoprotein family containing a diselenide bond in a redox motif.</Title>
-<Xref>DOI:10.1073/pnas.0703448104</Xref>
-<Xref>PMID:17715293</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Metanis, N.</Author>
-<Author>Keinan, E.</Author>
-<Author>Dawson, P.E.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 128, 16684-16691, 2006</Citation>
-<Title>Synthetic seleno-glutaredoxin 3 analogues are highly reducing oxidoreductases with enhanced catalytic efficiency.</Title>
-<Xref>DOI:10.1021/ja0661414</Xref>
-<Xref>PMID:17177418</Xref>
-<Note>comparative redox potentials of cystine, cysteinylselenocysteine and selenocystine in synthetic glutaredoxins with a [C/U]XX[C/U] motif</Note>
-</ReferenceBlock>
-<Comment>The experimental redox potential of selenocystine in synthetic glutaredoxin 3 is -309 mV. See RESID:AA0025 and RESID:AA0358.</Comment>
-<SequenceCode link="SEC2">
-<SequenceSpec>U, U</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:01183</Xref>
-</SequenceCode>
-<SequenceCode link="CYS2">
-<SequenceSpec>C, C</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Condition>secondary to RESID:AA0022</Condition>
-<Xref>PSI-MOD:01184</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>redox-active center</Keyword>
-<Keyword>selenium</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__selenocystine (sec-sec)__u__u">CROSSLNK Selenocystine (Sec-Sec)</Feature>
-</Features>
-<Image src="/images/AA0437.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0437.PDB" />
-</Entry>
-<Entry id="AA0438">
-<Header>
-<Code>AA0438</Code>
-<Dates>
-<CreationDate>31-Dec-2007</CreationDate>
-<StrucRevDate>31-Dec-2007</StrucRevDate>
-<TextChngDate>20-Apr-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>tris-L-cysteinyl L-histidino diiron disulfide</Name>
-<AlternateName>CDGSH domain iron-sulfur cluster</AlternateName>
-<SystematicName>di-mu-sulfido(bis-S-cysteinyliron)(S-cysteinyl-N3'-histidinoiron)</SystematicName>
-<Xref>PDBHET:FES</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 15 Fe 2 H 18 N 6 O 4 S 5</Formula>
-<FormalCharge>2-</FormalCharge>
-<Weight type="chemical">618.34</Weight>
-<Weight type="physical">617.870280</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005 AA0005 AA0009">
-<Formula>C 0 Fe 2 H -4 N 0 O 0 S 2</Formula>
-<FormalCharge>2-</FormalCharge>
-<Weight type="chemical">171.78</Weight>
-<Weight type="physical">171.783814</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Paddock, M.L.</Author>
-<Author>Wiley, S.E.</Author>
-<Author>Axelrod, H.L.</Author>
-<Author>Cohen, A.E.</Author>
-<Author>Roy, M.</Author>
-<Author>Abresch, E.C.</Author>
-<Author>Capraro, D.</Author>
-<Author>Murphy, A.N.</Author>
-<Author>Nechushtai, R.</Author>
-<Author>Dixon, J.E.</Author>
-<Author>Jennings, P.A.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 104, 14342-14347, 2007</Citation>
-<Title>MitoNEET is a uniquely folded 2Fe 2S outer mitochondrial membrane protein stabilized by pioglitazone.</Title>
-<Xref>DOI:10.1073/pnas.0707189104</Xref>
-<Xref>PMID:17766440</Xref>
-<Note>X-ray diffraction, 1.50 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Paddock, M.L.</Author>
-<Author>Wiley, S.E.</Author>
-<Author>Axelrod, H.L.</Author>
-<Author>Cohen, A.E.</Author>
-<Author>Roy, M.</Author>
-<Author>Abresch, E.C.</Author>
-<Author>Capraro, D.</Author>
-<Author>Murphy, A.N.</Author>
-<Author>Nechushtai, R.</Author>
-<Author>Dixon, J.E.</Author>
-<Author>Jennings, P.A.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, June 2007</Citation>
-<Description>MitoNEET is a uniquely folded 2Fe 2S outer mitochondrial membrane protein stabilized by pioglitazone.</Description>
-<Xref>PDB:2QH7</Xref>
-<Note>X-ray diffraction, 1.50 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lin, J.</Author>
-<Author>Zhou, T.</Author>
-<Author>Ye, K.</Author>
-<Author>Wang, J.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 104, 14640-14645, 2007</Citation>
-<Title>Crystal structure of human mitoNEET reveals distinct groups of iron sulfur proteins.</Title>
-<Xref>DOI:10.1073/pnas.0702426104</Xref>
-<Xref>PMID:17766439</Xref>
-<Note>X-ray diffraction, 1.81 angstroms</Note>
-</ReferenceBlock>
-<Comment>The CDGSH homology domain containing this iron-sulfur cluster had been predicted to be a "zinc finger".</Comment>
-<SequenceCode>
-<SequenceSpec>C, C, C, H</SequenceSpec>
-<Condition>cross-link 4</Condition>
-<Xref>PSI-MOD:00864</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>2Fe-2S</Keyword>
-<Keyword>iron-sulfur protein</Keyword>
-<Keyword>metalloprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="metal__iron-sulfur (2fe-2s)__c">METAL Iron-sulfur (2Fe-2S)</Feature>
-<Feature type="UniProt" key="metal__iron-sulfur (2fe-2s); via pros nitrogen__h">METAL Iron-sulfur (2Fe-2S); via pros nitrogen</Feature>
-</Features>
-<Image src="/images/AA0438.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0438.PDB" />
-</Entry>
-<Entry id="AA0439">
-<Header>
-<Code>AA0439</Code>
-<Dates>
-<CreationDate>31-Dec-2007</CreationDate>
-<StrucRevDate>31-Dec-2007</StrucRevDate>
-<TextChngDate>30-Apr-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-aspartyl-glycosylsphingolipidinositolethanolamine</Name>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 12 N 2 O 7 P 1 +</Formula>
-<Weight type="chemical">255.14 +</Weight>
-<Weight type="physical">255.038212 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0004">
-<Formula>C 2 H 6 N 1 O 3 P 1 +</Formula>
-<Weight type="chemical">123.05 +</Weight>
-<Weight type="physical">123.008530 +</Weight>
-</CorrectionBlock>
-<Comment>This modification is predicted for proteins with sequence characteristics for the GPI-like anchor modification with sphingolipid, and with asparatic acid at the cleavage and anchor attachment site.</Comment>
-<Comment>A representative glycan core structure is shown.</Comment>
-<Comment>Cleavage of a carboxyl terminal propeptide accompanies transamidation.</Comment>
-<SequenceCode>
-<SequenceSpec>D</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>PSI-MOD:00865</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>glycoprotein</Keyword>
-<Keyword>lipoprotein</Keyword>
-<Keyword>phosphoprotein</Keyword>
-<Keyword>sphingolipidinositol linkage</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__gpi-like-anchor amidated aspartate__n">LIPID GPI-like-anchor amidated aspartate</Feature>
-</Features>
-<Image src="/images/AA0439.GIF" alt="DUMMY.GIF" />
-</Entry>
-<Entry id="AA0440">
-<Header>
-<Code>AA0440</Code>
-<Dates>
-<CreationDate>31-Mar-2008</CreationDate>
-<StrucRevDate>31-Mar-2008</StrucRevDate>
-<TextChngDate>26-Feb-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6-(L-threonyl)-L-lysine</Name>
-<AlternateName>N6-threonyl-lysine</AlternateName>
-<SystematicName>(2S)-2-amino-6-([(2S,3R)-2-amino-3-hydroxybutanoyl]amino)hexanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 10 H 18 N 3 O 3</Formula>
-<Weight type="chemical">228.27</Weight>
-<Weight type="physical">228.134816</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012 AA0017">
-<Formula>C 0 H -2 N 0 O -1</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kang, H.J.</Author>
-<Author>Coulibaly, F.</Author>
-<Author>Clow, F.</Author>
-<Author>Proft, T.</Author>
-<Author>Baker, E.N.</Author>
-</Authors>
-<Citation>Science 318, 1625-1628, 2007</Citation>
-<Title>Stabilizing isopeptide bonds revealed in gram-positive bacterial pilus structure.</Title>
-<Xref>DOI:10.1126/science.1145806</Xref>
-<Xref>PMID:18063798</Xref>
-<Note>X-ray diffraction, 2.2 angstroms; evidence for multiple intrachain isoaspartyl lysine isopeptide cross-links</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kang, H.J.</Author>
-<Author>Coulibaly, F.</Author>
-<Author>Proft, T.</Author>
-<Author>Baker, E.N.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, October 2007</Citation>
-<Description>Crystal structure of the major pilin from Streptococcus pyogenes.</Description>
-<Xref>PDB:3B2M</Xref>
-<Note>X-ray diffraction, 2.22 angstroms</Note>
-</ReferenceBlock>
-<Comment>This interchain cross-link is formed between a lysine residue and a threonine residue in polymerized streptococcal pilin.</Comment>
-<SequenceCode>
-<SequenceSpec>K, T</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Condition>cross-link 2</Condition>
-<Condition>incidental to RESID:AA0345</Condition>
-<Xref>PSI-MOD:00924</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>isopeptide bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__threonyl lysine isopeptide (lys-thr) (interchain with t-__k">CROSSLNK Threonyl lysine isopeptide (Lys-Thr) (interchain with T-...)</Feature>
-<Feature type="UniProt" key="crosslnk__threonyl lysine isopeptide (thr-lys) (interchain with k-__t">CROSSLNK Threonyl lysine isopeptide (Thr-Lys) (interchain with K-...)</Feature>
-</Features>
-<Image src="/images/AA0440.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0440.PDB" />
-</Entry>
-<Entry id="AA0441">
-<Header>
-<Code>AA0441</Code>
-<Dates>
-<CreationDate>31-Mar-2008</CreationDate>
-<StrucRevDate>31-Mar-2008</StrucRevDate>
-<TextChngDate>30-Jun-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>(2-aminosuccinimidyl)acetic acid</Name>
-<AlternateName>(3-amino-2,5-dioxo-1-pyrrolidinyl)acetic acid</AlternateName>
-<AlternateName>anhydroaspartyl glycine</AlternateName>
-<AlternateName>aspartimide glycine</AlternateName>
-<AlternateName>N-(2-aminosuccinyl)glycine</AlternateName>
-<SystematicName>[(3S)-3-amino-2,5-dioxopyrrolidin-1-yl]acetic acid</SystematicName>
-<Xref>ChEBI:45890</Xref>
-<Xref>PDBHET:ACY</Xref>
-<Xref>PDBHET:SNN</Xref>
-<Xref>PDBHET:SUI</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 6 N 2 O 3</Formula>
-<Weight type="chemical">154.13</Weight>
-<Weight type="physical">154.037842</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0003 AA0008" label="ASN">
-<Formula>C 0 H -3 N -1 O 0</Formula>
-<Weight type="chemical">-17.03</Weight>
-<Weight type="physical">-17.026549</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0004 AA0008" label="ASP">
-<Formula>C 0 H -2 N 0 O -1</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Anonymous />
-<Group>IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN)</Group>
-</Authors>
-<Citation>Eur. J. Biochem. 183, 1-4, 1989</Citation>
-<Title>Nomenclature Committee of IUB (NC-IUB) and IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN), newsletter 1989.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1989.tb14887.x</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Højrup, P.</Author>
-<Author>Gerola, P.</Author>
-<Author>Hansen, H.F.</Author>
-<Author>Mikkelsen, J.M.</Author>
-<Author>Shahed, A.E.</Author>
-<Author>Knudsen, J.</Author>
-<Author>Roepstorff, P.</Author>
-<Author>Olson, J.M.</Author>
-</Authors>
-<Citation>Biochim. Biophys. Acta 1077, 220-224, 1991</Citation>
-<Title>The amino acid sequence of a major protein component in the light harvesting complex of the green photosynthetic bacterium Chlorobium limicola f. thiosulfatophilum.</Title>
-<Xref>DOI:10.1016/0167-4838(91)90061-4</Xref>
-<Xref>PMID:2015294</Xref>
-<Note>detection of a blocked N-terminal Asn-Gly sequence with a mass loss of "approx. 18 Da"; the formation of (2-aminosuccinimidyl)acetic acid, with a mass loss of 17 Da, would probably block imidazolinone cyclization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hernandez, J.F.</Author>
-<Author>Gagnon, J.</Author>
-<Author>Chiche, L.</Author>
-<Author>Nguyen, T.M.</Author>
-<Author>Andrieu, J.P.</Author>
-<Author>Heitz, A.</Author>
-<Author>Trinh Hong, T.</Author>
-<Author>Pham, T.T.</Author>
-<Author>Le Nguyen, D.</Author>
-</Authors>
-<Citation>Biochemistry 39, 5722-5730, 2000</Citation>
-<Title>Squash trypsin inhibitors from Momordica cochinchinensis exhibit an atypical macrocyclic structure.</Title>
-<Xref>DOI:10.1021/bi9929756 S0006-2960(99)02975-X</Xref>
-<Xref>PMID:10801322</Xref>
-<Note>probable mass spectrometric detection of cyclic anhydride formed from aspartic acid</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fitzgerald, P.M.D.</Author>
-<Author>Sharma, N.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, July 2001</Citation>
-<Description>IMP-1 metallo beta-lactamase from Pseudomonas aeruginosa in complex with a biaryl succinic acid inhibitor (1).</Description>
-<Xref>PDB:1JJT</Xref>
-<Note>X-ray diffraction, 1.80 angstroms; the cross-link is mentioned in the PDB entry and not in the publication</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Erskine, P.T.</Author>
-<Author>Coates, L.</Author>
-<Author>Mall, S.</Author>
-<Author>Gill, R.S.</Author>
-<Author>Wood, S.P.</Author>
-<Author>Myles, D.A.A.</Author>
-<Author>Cooper, J.B.</Author>
-</Authors>
-<Citation>Protein Sci. 12, 1741-1749, 2003</Citation>
-<Title>Atomic resolution analysis of the catalytic site of an aspartic proteinase and an unexpected mode of binding by short peptides.</Title>
-<Xref>DOI:10.1110/ps.0305203</Xref>
-<Xref>PMID:12876323</Xref>
-<Note>X-ray diffraction, 0.9 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Coates, L.</Author>
-<Author>Erskine, P.T.</Author>
-<Author>Mall, S.</Author>
-<Author>Gill, R.S.</Author>
-<Author>Wood, S.P.</Author>
-<Author>Myles, D.A.A.</Author>
-<Author>Cooper, J.B.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, March 2003</Citation>
-<Description>Atomic resolution structure of native endothiapepsin.</Description>
-<Xref>PDB:1OEW</Xref>
-<Note>X-ray diffraction, 0.9 angstroms</Note>
-</ReferenceBlock>
-<Comment>This cross-link is formed by the condensation of an aspartic acid or asparagine residue with the alpha-amido of the following residue.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode link="ASN">
-<SequenceSpec>G, N</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Xref>PSI-MOD:01624</Xref>
-</SequenceCode>
-<SequenceCode link="ASP">
-<SequenceSpec>D, G</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Xref>PSI-MOD:00952</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>succinimide ring</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__(2-aminosuccinimidyl)acetic acid (asn-gly)__n__g" link="ASN">CROSSLNK (2-aminosuccinimidyl)acetic acid (Asn-Gly)</Feature>
-<Feature type="UniProt" key="crosslnk__(2-aminosuccinimidyl)acetic acid (asp-gly)__d__g" link="ASP">CROSSLNK (2-aminosuccinimidyl)acetic acid (Asp-Gly)</Feature>
-</Features>
-<Image src="/images/AA0441.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0441.PDB" />
-</Entry>
-<Entry id="AA0442">
-<Header>
-<Code>AA0442</Code>
-<Dates>
-<CreationDate>08-Aug-2008</CreationDate>
-<StrucRevDate>08-Aug-2008</StrucRevDate>
-<TextChngDate>30-Jan-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>(2S)-4-hydroxyleucine</Name>
-<AlternateName>gamma-hydroxyleucine</AlternateName>
-<SystematicName>(2S)-2-amino-4-hydroxy-4-methylpentanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 11 N 1 O 2</Formula>
-<Weight type="chemical">129.16</Weight>
-<Weight type="physical">129.078979</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0011">
-<Formula>C 0 H 0 N 0 O 1</Formula>
-<Weight type="chemical">16.00</Weight>
-<Weight type="physical">15.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wieland, T.</Author>
-<Author>Faulstich, H.</Author>
-</Authors>
-<Citation>C.R.C. Crit. Rev. Biochem. 5, 185-260, 1978</Citation>
-<Title>Amatoxins, phallotoxins, phallolysin, and antamanide: the biologically active components of poisonous Amanita mushrooms.</Title>
-<Xref>PMID:363352</Xref>
-<Note>described as a constituent of the phallotoxin phalloin</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fu, S.L.</Author>
-<Author>Dean, R.T.</Author>
-</Authors>
-<Citation>Biochem. J. 324, 41-48, 1997</Citation>
-<Title>Structural characterization of the products of hydroxyl-radical damage to leucine and their detection on proteins.</Title>
-<Xref>PMID:9164839</Xref>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>L</SequenceSpec>
-<Xref>PSI-MOD:01372</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0442.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0442.PDB" />
-</Entry>
-<Entry id="AA0443">
-<Header>
-<Code>AA0443</Code>
-<Dates>
-<CreationDate>08-Aug-2008</CreationDate>
-<StrucRevDate>08-Aug-2008</StrucRevDate>
-<TextChngDate>30-Sep-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>(2S,4R)-5-hydroxyleucine</Name>
-<AlternateName>(4R)-5-hydroxyleucine</AlternateName>
-<AlternateName>delta-hydroxyleucine</AlternateName>
-<SystematicName>(2S,4R)-2-amino-5-hydroxy-4-methylpentanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 11 N 1 O 2</Formula>
-<Weight type="chemical">129.16</Weight>
-<Weight type="physical">129.078979</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0011">
-<Formula>C 0 H 0 N 0 O 1</Formula>
-<Weight type="chemical">16.00</Weight>
-<Weight type="physical">15.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wilson, J.B.</Author>
-<Author>Brennan, S.O.</Author>
-<Author>Allen, J.</Author>
-<Author>Shaw, J.G.</Author>
-<Author>Gu, L.H.</Author>
-<Author>Huisman, T.H.</Author>
-</Authors>
-<Citation>J. Chromatogr. 617, 37-42, 1993</Citation>
-<Title>The M gamma chain of human fetal hemoglobin is an A gamma chain with an in vitro modification of gamma 141 leucine to hydroxyleucine.</Title>
-<Xref>DOI:10.1016/0378-4347(93)80418-4</Xref>
-<Xref>PMID:7690768</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fu, S.L.</Author>
-<Author>Dean, R.T.</Author>
-</Authors>
-<Citation>Biochem. J. 324, 41-48, 1997</Citation>
-<Title>Structural characterization of the products of hydroxyl-radical damage to leucine and their detection on proteins.</Title>
-<Xref>PMID:9164839</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sundheim, O.</Author>
-<Author>Vågbø, C.B.</Author>
-<Author>Bjørås, M.</Author>
-<Author>Sousa, M.M.L.</Author>
-<Author>Talstad, V.</Author>
-<Author>Aas, P.A.</Author>
-<Author>Drabløs, F.</Author>
-<Author>Krokan, H.E.</Author>
-<Author>Tainer, J.A.</Author>
-<Author>Slupphaug, G.</Author>
-</Authors>
-<Citation>EMBO J. 25, 3389-3397, 2006</Citation>
-<Title>Human ABH3 structure and key residues for oxidative demethylation to reverse DNA/RNA damage.</Title>
-<Xref>DOI:10.1038/sj.emboj.7601219</Xref>
-<Xref>PMID:16858410</Xref>
-<Note>X-ray diffraction, 1.50 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sundheim, O.</Author>
-<Author>Vagbo, C.B.</Author>
-<Author>Bjoras, M.</Author>
-<Author>DeSousa, M.M.L.</Author>
-<Author>Talstad, V.</Author>
-<Author>Aas, P.A.</Author>
-<Author>Drablos, F.</Author>
-<Author>Krokan, H.E.</Author>
-<Author>Tainer, J.A.</Author>
-<Author>Slupphaug, G.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, June 2006</Citation>
-<Description>Human ABH3 structure and key residues for oxidative demethylation to reverse DNA/RNA damage.</Description>
-<Xref>PDB:2IUW</Xref>
-<Note>X-ray diffraction, 1.50 angstroms</Note>
-</ReferenceBlock>
-<Comment>The oxidation artifacts 5-hydroxyleucine and 5-oxoleucine can form autocatalytically and stereospecifically, but not selectively. It is not clear whether the modified residue subsequently takes part in catalytic reactions at the active site of alpha-ketoglutarate-dependent dioxygenase alkB homolog 3 (ABH3).</Comment>
-<SequenceCode>
-<SequenceSpec>L</SequenceSpec>
-<Xref>PSI-MOD:01373</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0443.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0443.PDB" />
-</Entry>
-<Entry id="AA0444">
-<Header>
-<Code>AA0444</Code>
-<Dates>
-<CreationDate>08-Aug-2008</CreationDate>
-<StrucRevDate>08-Aug-2008</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>(2S,4R)-5-oxoleucine</Name>
-<AlternateName>(4R)-5-oxo-L-leucine</AlternateName>
-<SystematicName>(2S,4R)-2-amino-4-methyl-5-oxopentanoic acid</SystematicName>
-<Xref>ChEBI:43739</Xref>
-<Xref>PDBHET:LED</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 9 N 1 O 2</Formula>
-<Weight type="chemical">127.14</Weight>
-<Weight type="physical">127.063329</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0011">
-<Formula>C 0 H -2 N 0 O 1</Formula>
-<Weight type="chemical">13.98</Weight>
-<Weight type="physical">13.979265</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sundheim, O.</Author>
-<Author>Vågbø, C.B.</Author>
-<Author>Bjørås, M.</Author>
-<Author>Sousa, M.M.L.</Author>
-<Author>Talstad, V.</Author>
-<Author>Aas, P.A.</Author>
-<Author>Drabløs, F.</Author>
-<Author>Krokan, H.E.</Author>
-<Author>Tainer, J.A.</Author>
-<Author>Slupphaug, G.</Author>
-</Authors>
-<Citation>EMBO J. 25, 3389-3397, 2006</Citation>
-<Title>Human ABH3 structure and key residues for oxidative demethylation to reverse DNA/RNA damage.</Title>
-<Xref>DOI:10.1038/sj.emboj.7601219</Xref>
-<Xref>PMID:16858410</Xref>
-<Note>X-ray diffraction, 1.50 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sundheim, O.</Author>
-<Author>Vagbo, C.B.</Author>
-<Author>Bjoras, M.</Author>
-<Author>DeSousa, M.M.L.</Author>
-<Author>Talstad, V.</Author>
-<Author>Aas, P.A.</Author>
-<Author>Drablos, F.</Author>
-<Author>Krokan, H.E.</Author>
-<Author>Tainer, J.A.</Author>
-<Author>Slupphaug, G.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, June 2006</Citation>
-<Description>Human ABH3 structure and key residues for oxidative demethylation to reverse DNA/RNA damage.</Description>
-<Xref>PDB:2IUW</Xref>
-<Note>X-ray diffraction, 1.50 angstroms</Note>
-</ReferenceBlock>
-<Comment>The oxidation artifacts 5-hydroxyleucine and 5-oxoleucine can form autocatalytically and stereospecifically, but not selectively. It is not clear whether the modified residue subsequently takes part in catalytic reactions at the active site of alpha-ketoglutarate-dependent dioxygenase alkB homolog 3 (ABH3).</Comment>
-<SequenceCode>
-<SequenceSpec>L</SequenceSpec>
-<Xref>PSI-MOD:01374</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Features>
-<Feature type="UniProt" key="mod_res__(4r)-5-oxoleucine__l">MOD_RES (4R)-5-oxoleucine</Feature>
-</Features>
-<Image src="/images/AA0444.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0444.PDB" />
-</Entry>
-<Entry id="AA0445">
-<Header>
-<Code>AA0445</Code>
-<Dates>
-<CreationDate>08-Aug-2008</CreationDate>
-<StrucRevDate>08-Aug-2008</StrucRevDate>
-<TextChngDate>30-Jan-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>(2S,4R)-4,5-dihydroxyleucine</Name>
-<AlternateName>(4R)-4,5-dihydroxyleucine</AlternateName>
-<AlternateName>gamma,delta-dihydroxyleucine</AlternateName>
-<SystematicName>(2S,4R)-2-amino-4,5-dihydroxy-4-methylpentanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 11 N 1 O 3</Formula>
-<Weight type="chemical">145.16</Weight>
-<Weight type="physical">145.073893</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0011">
-<Formula>C 0 H 0 N 0 O 2</Formula>
-<Weight type="chemical">32.00</Weight>
-<Weight type="physical">31.989829</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Georgi, V.</Author>
-<Author>Wieland, T.</Author>
-</Authors>
-<Citation>Justus Liebigs Ann. Chem. 700, 149-156, 1966</Citation>
-<Title>Über die Inhaltsstoffe des grünen Knollenblätterpilzes. XXIX. Synthese von gamma-delta-Dihydroxy-isoleucin, der lactonisierenden Aminosäure von alpha- und beta-Amanitin. [On the ingredients of the green amanita. XXIX. Synthesis of gamma-delta-dihydroxyleucine, the lactonizing amino acid of alpha- and beta-amanitin].</Title>
-<Xref>DOI:10.1002/jlac.19667000118</Xref>
-<Xref>PMID:6010785</Xref>
-<Note>article in German</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Faulstich, H.</Author>
-<Author>Buku, A.</Author>
-<Author>Bodenmüller, H.</Author>
-<Author>Wieland, T.</Author>
-</Authors>
-<Citation>Biochemistry 19, 3334-3343, 1980</Citation>
-<Title>Virotoxins: actin-binding cyclic peptides of Amanita virosa mushrooms.</Title>
-<Xref>DOI:10.1021/bi00555a036</Xref>
-<Xref>PMID:6893271</Xref>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>L</SequenceSpec>
-<Xref>PSI-MOD:01375</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__(4r)-4,5-dihydroxyleucine__l">MOD_RES (4R)-4,5-dihydroxyleucine</Feature>
-</Features>
-<Image src="/images/AA0445.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0445.PDB" />
-</Entry>
-<Entry id="AA0446">
-<Header>
-<Code>AA0446</Code>
-<Dates>
-<CreationDate>31-Mar-2009</CreationDate>
-<StrucRevDate>31-Mar-2009</StrucRevDate>
-<TextChngDate>30-Jun-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>(2S,4S)-4,5-dihydroxyleucine</Name>
-<AlternateName>(4S)-4,5-dihydroxyleucine</AlternateName>
-<AlternateName>gamma,delta-dihydroxyleucine</AlternateName>
-<SystematicName>(2S,4S)-2-amino-4,5-dihydroxy-4-methylpentanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 11 N 1 O 3</Formula>
-<Weight type="chemical">145.16</Weight>
-<Weight type="physical">145.073893</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0011">
-<Formula>C 0 H 0 N 0 O 2</Formula>
-<Weight type="chemical">32.00</Weight>
-<Weight type="physical">31.989829</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Little, M.C.</Author>
-<Author>Preston III, J.F.</Author>
-<Author>Jackson, C.</Author>
-<Author>Bonetti, S.</Author>
-<Author>King, R.W.</Author>
-<Author>Taylor, L.C.</Author>
-</Authors>
-<Citation>Biochemistry 25, 2867-2872, 1986</Citation>
-<Title>Alloviroidin, the naturally occurring toxic isomer of the cyclopeptide viroidin.</Title>
-<Xref>DOI:10.1021/bi00358a019</Xref>
-<Xref>PMID:3718926</Xref>
-<Note>the name of J.F. Preston III in the PubMed citation is corrected</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>L</SequenceSpec>
-<Xref>PSI-MOD:01432</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0446.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0446.PDB" />
-</Entry>
-<Entry id="AA0447">
-<Header>
-<Code>AA0447</Code>
-<Dates>
-<CreationDate>24-Oct-2008</CreationDate>
-<StrucRevDate>24-Oct-2008</StrucRevDate>
-<TextChngDate>30-Apr-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>(2S,3S,4R)-3,4-dihydroxyisoleucine</Name>
-<AlternateName>(3S,4R)-3,4-dihydroxyisoleucine</AlternateName>
-<AlternateName>beta,gamma-dihydroxyisoleucine</AlternateName>
-<SystematicName>(2S,3S,4R)-2-amino-3,4-dihydroxy-3-methylpentanoic acid</SystematicName>
-<Xref>PDBHET:TSI</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 11 N 1 O 3</Formula>
-<Weight type="chemical">145.16</Weight>
-<Weight type="physical">145.073893</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0010">
-<Formula>C 0 H 0 N 0 O 2</Formula>
-<Weight type="chemical">32.00</Weight>
-<Weight type="physical">31.989829</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bond, C.S.</Author>
-<Author>Shaw, M.P.</Author>
-<Author>Alphey, M.S.</Author>
-<Author>Hunter, W.N.</Author>
-</Authors>
-<Citation>Acta Crystallogr. D Biol. Crystallogr. 57, 755-758, 2001</Citation>
-<Title>Structure of the macrocycle thiostrepton solved using the anomalous dispersion contribution of sulfur.</Title>
-<Xref>DOI:10.1107/S0907444901003134</Xref>
-<Xref>PMID:11320328</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bond, C.S.</Author>
-<Author>Shaw, M.P.</Author>
-<Author>Alphey, M.S.</Author>
-<Author>Hunter, W.N.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, October 2000</Citation>
-<Description>Structure of the macrocycle thiostrepton solved using the anomalous dispersion contribution of sulfur.</Description>
-<Xref>PDB:1E9W</Xref>
-<Note>X-ray diffraction, 1.02 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mukai, A.</Author>
-<Author>Fukai, T.</Author>
-<Author>Hoshino, Y.</Author>
-<Author>Yazawa, K.</Author>
-<Author>Harada, K.-I.</Author>
-<Author>Mikami, Y.</Author>
-</Authors>
-<Citation>J. Antibiot. 62, 613-619, 2009</Citation>
-<Title>Nocardithiocin, a novel thiopeptide antibiotic, produced by pathogenic Nocardia pseudobrasiliensis IFM 0757.</Title>
-<Xref>DOI:10.1038/ja.2009.90</Xref>
-<Xref>PMID:19745839</Xref>
-<Note>the initials of K.-I. Harada in the PubMed citation are corrected</Note>
-</ReferenceBlock>
-<Comment>In some cases the stereochemistry for the second and third chiral centers have not been resolved.</Comment>
-<SequenceCode>
-<SequenceSpec>I</SequenceSpec>
-<Condition>incidental to RESID:AA0466</Condition>
-<Xref>PSI-MOD:01376</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__(3s,4r)-3,4-dihydroxyisoleucine__i">MOD_RES (3S,4R)-3,4-dihydroxyisoleucine</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="mod_res__3,4-dihydroxyisoleucine__i">MOD_RES 3,4-dihydroxyisoleucine</Feature>
-<Note>this UniProt feature is used when the stereochemistry has not been determined</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0447.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0447.PDB" />
-</Entry>
-<Entry id="AA0448">
-<Header>
-<Code>AA0448</Code>
-<Dates>
-<CreationDate>08-Aug-2008</CreationDate>
-<StrucRevDate>08-Aug-2008</StrucRevDate>
-<TextChngDate>30-Sep-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>(2S,3R,4S)-4-hydroxyisoleucine</Name>
-<AlternateName>(2S,3R,4S)-2-amino-3-methyl-4-hydroxyvaleric acid</AlternateName>
-<AlternateName>(3R,4S)-4-hydroxyisoleucine</AlternateName>
-<AlternateName>gamma-hydroxyisoleucine</AlternateName>
-<SystematicName>(2S,3R,4S)-2-amino-4-hydroxy-3-methylpentanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 11 N 1 O 2</Formula>
-<Weight type="chemical">129.16</Weight>
-<Weight type="physical">129.078979</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0010">
-<Formula>C 0 H 0 N 0 O 1</Formula>
-<Weight type="chemical">16.00</Weight>
-<Weight type="physical">15.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gieren, A.</Author>
-<Author>Narayana, P.</Author>
-<Author>Hoppe, W.</Author>
-<Author>Hasan, M.</Author>
-<Author>Michl, K.</Author>
-<Author>Wieland, T.</Author>
-<Author>Smith, H.O.</Author>
-<Author>Jung, G.</Author>
-<Author>Breitmai, E.</Author>
-</Authors>
-<Citation>Justus Liebigs Ann. Chem. 1974, 1561-1569, 1974</Citation>
-<Title>Über die Inhaltsstoffe des grünen Knollenblätterpilzes. XLIV. Die Konfiguration der hydroxylierten Isoleucine der Amatoxine. [Components of Green Deathcap Toadstool, Amanita Phalloides. XLIV. Configuration of hydroxylated isoleucines from Amatoxins].</Title>
-<Xref>DOI:10.1002/jlac.197419741004</Xref>
-<Note>article in German</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wieland, T.</Author>
-<Author>Faulstich, H.</Author>
-</Authors>
-<Citation>C.R.C. Crit. Rev. Biochem. 5, 185-260, 1978</Citation>
-<Title>Amatoxins, phallotoxins, phallolysin, and antamanide: the biologically active components of poisonous Amanita mushrooms.</Title>
-<Xref>PMID:363352</Xref>
-<Note>described as a constituent of the amatoxin gamma-amanitin</Note>
-</ReferenceBlock>
-<Comment>In peptide sequencing work prior to 1968, this modification was reported as a beta-methylleucine derivative that could arise by either beta-methylation of leucine or gamma-methylation of isoleucine. The correct structure has been determined to be derived from isoleucine without methylation.</Comment>
-<SequenceCode>
-<SequenceSpec>I</SequenceSpec>
-<Xref>PSI-MOD:01377</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__(3r,4s)-4-hydroxyisoleucine__i">MOD_RES (3R,4S)-4-hydroxyisoleucine</Feature>
-</Features>
-<Image src="/images/AA0448.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0448.PDB" />
-</Entry>
-<Entry id="AA0449">
-<Header>
-<Code>AA0449</Code>
-<Dates>
-<CreationDate>08-Aug-2008</CreationDate>
-<StrucRevDate>08-Aug-2008</StrucRevDate>
-<TextChngDate>30-Sep-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>(2S,3R,4R)-4,5-dihydroxyisoleucine</Name>
-<AlternateName>(3R,4R)-4,5-dihydroxyisoleucine</AlternateName>
-<AlternateName>gamma,delta-dihydroxyisoleucine</AlternateName>
-<SystematicName>(2S,3R,4R)-2-amino-4,5-dihydroxy-3-methylpentanoic acid</SystematicName>
-<Xref>PDBHET:ILX</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 11 N 1 O 3</Formula>
-<Weight type="chemical">145.16</Weight>
-<Weight type="physical">145.073893</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0010">
-<Formula>C 0 H 0 N 0 O 2</Formula>
-<Weight type="chemical">32.00</Weight>
-<Weight type="physical">31.989829</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gieren, A.</Author>
-<Author>Narayana, P.</Author>
-<Author>Hoppe, W.</Author>
-<Author>Hasan, M.</Author>
-<Author>Michl, K.</Author>
-<Author>Wieland, T.</Author>
-<Author>Smith, H.O.</Author>
-<Author>Jung, G.</Author>
-<Author>Breitmai, E.</Author>
-</Authors>
-<Citation>Justus Liebigs Ann. Chem. 1974, 1561-1569, 1974</Citation>
-<Title>Über die Inhaltsstoffe des grünen Knollenblätterpilzes, XLIV. Die Konfiguration der hydroxylierten Isoleucine der Amatoxine. [Components of Green Deathcap Toadstool, Amanita Phalloides. XLIV. Configuration of hydroxylated isoleucines from Amatoxins].</Title>
-<Xref>DOI:10.1002/jlac.197419741004</Xref>
-<Note>article in German</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wieland, T.</Author>
-<Author>Faulstich, H.</Author>
-</Authors>
-<Citation>C.R.C. Crit. Rev. Biochem. 5, 185-260, 1978</Citation>
-<Title>Amatoxins, phallotoxins, phallolysin, and antamanide: the biologically active components of poisonous Amanita mushrooms.</Title>
-<Xref>PMID:363352</Xref>
-<Note>described as a constituent of the amatoxin alpha-amanitin</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bushnell, D.A.</Author>
-<Author>Cramer, P.</Author>
-<Author>Kornberg, R.D.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 99, 1218-1222, 2002</Citation>
-<Title>Structural basis of transcription: alpha-amanitin-RNA polymerase II cocrystal at 2.8 A resolution.</Title>
-<Xref>DOI:10.1073/pnas.251664698</Xref>
-<Xref>PMID:11805306</Xref>
-<Note>X-ray diffraction with modeled peptide, 2.80 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bushnell, D.A.</Author>
-<Author>Cramer, P.</Author>
-<Author>Kornberg, R.D.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, October 2001</Citation>
-<Description>Crystal structure of yeast RNA polymerase II complexed with the inhibitor alpha amanitin.</Description>
-<Xref>PDB:1K83</Xref>
-<Note>X-ray diffraction with modeled peptide, 2.80 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Brueckner, F.</Author>
-<Author>Cramer, P.</Author>
-</Authors>
-<Citation>Nature Struct. Mol. Biol. 15, 811-818, 2008</Citation>
-<Title>Structural basis of transcription inhibition by alpha-amanitin and implications for RNA polymerase II translocation.</Title>
-<Xref>DOI:10.1038/nsmb.1458</Xref>
-<Xref>PMID:18552824</Xref>
-<Note>X-ray diffraction, 3.40 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Brueckner, F.</Author>
-<Author>Cramer, P.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, May 2008</Citation>
-<Description>Alpha-amanitin inhibited complete RNA polymerase II elongation complex.</Description>
-<Xref>PDB:2VUM</Xref>
-<Note>X-ray diffraction, 3.40 angstroms</Note>
-</ReferenceBlock>
-<Comment>In peptide sequencing work prior to 1968, this modification was reported as a beta-methylleucine derivative that could arise by either beta-methylation of leucine or gamma-methylation of isoleucine. The correct structure has been determined to be derived from isoleucine without methylation.</Comment>
-<SequenceCode>
-<SequenceSpec>I</SequenceSpec>
-<Xref>PSI-MOD:01378</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__(3r,4r)-4,5-dihydroxyisoleucine__i">MOD_RES (3R,4R)-4,5-dihydroxyisoleucine</Feature>
-</Features>
-<Image src="/images/AA0449.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0449.PDB" />
-</Entry>
-<Entry id="AA0450">
-<Header>
-<Code>AA0450</Code>
-<Dates>
-<CreationDate>08-Aug-2008</CreationDate>
-<StrucRevDate>08-Aug-2008</StrucRevDate>
-<TextChngDate>30-Jan-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>2'-methylsulfonyl-L-tryptophan</Name>
-<SystematicName>2-methylsulfonyl-3-((2S)-2-amino-2-carboxyethyl)-1H-indole</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 12 H 12 N 2 O 3 S 1</Formula>
-<Weight type="chemical">264.30</Weight>
-<Weight type="physical">264.056863</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0018">
-<Formula>C 1 H 2 N 0 O 2 S 1</Formula>
-<Weight type="chemical">78.09</Weight>
-<Weight type="physical">77.977550</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Faulstich, H.</Author>
-<Author>Buku, A.</Author>
-<Author>Bodenmüller, H.</Author>
-<Author>Wieland, T.</Author>
-</Authors>
-<Citation>Biochemistry 19, 3334-3343, 1980</Citation>
-<Title>Virotoxins: actin-binding cyclic peptides of Amanita virosa mushrooms.</Title>
-<Xref>DOI:10.1021/bi00555a036</Xref>
-<Xref>PMID:6893271</Xref>
-</ReferenceBlock>
-<Comment>In virotoxin this modified tryptophan is formed after a 2'-(S-cysteinyl)tryptophan crosslink is broken.</Comment>
-<SequenceCode>
-<SequenceSpec>W</SequenceSpec>
-<Xref>PSI-MOD:01379</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="mod_res__2'-methylsulfonyltryptophan__w">MOD_RES 2'-methylsulfonyltryptophan</Feature>
-</Features>
-<Image src="/images/AA0450.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0450.PDB" />
-</Entry>
-<Entry id="AA0451">
-<Header>
-<Code>AA0451</Code>
-<Dates>
-<CreationDate>08-Aug-2008</CreationDate>
-<StrucRevDate>08-Aug-2008</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>2'-(S-L-cysteinyl)-6'-hydroxy-L-tryptophan sulfoxide</Name>
-<AlternateName>6'-hydroxy-S-oxo-tryptathionine</AlternateName>
-<SystematicName>2-{(R)-[(2R)-2-amino-2-carboxyethyl]sulfinyl}-3-[(2S)-2-amino-2-carboxyethyl]-6-hydroxy-1H-indole</SystematicName>
-<Xref>PDBHET:CSX</Xref>
-<Xref>PDBHET:TRX</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 14 H 13 N 3 O 4 S 1</Formula>
-<Weight type="chemical">319.33</Weight>
-<Weight type="physical">319.062677</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0018">
-<Formula>C 0 H -2 N 0 O 2 S 0</Formula>
-<Weight type="chemical">29.98</Weight>
-<Weight type="physical">29.974179</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wieland, T.</Author>
-</Authors>
-<Citation>Science 159, 946-952, 1968</Citation>
-<Title>Poisonous principles of mushrooms of the genus Amanita. Four-carbon amines acting on the central nervous system and cell-destroying cyclic peptides are produced.</Title>
-<Xref>DOI:10.1126/science.159.3818.946</Xref>
-<Xref>PMID:4865716</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wieland, T.</Author>
-<Author>Faulstich, H.</Author>
-</Authors>
-<Citation>C.R.C. Crit. Rev. Biochem. 5, 185-260, 1978</Citation>
-<Title>Amatoxins, phallotoxins, phallolysin, and antamanide: the biologically active components of poisonous Amanita mushrooms.</Title>
-<Xref>PMID:363352</Xref>
-<Note>described as a constituent of the amatoxins alpha- and gamma-amanitin</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bushnell, D.A.</Author>
-<Author>Cramer, P.</Author>
-<Author>Kornberg, R.D.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 99, 1218-1222, 2002</Citation>
-<Title>Structural basis of transcription: alpha-amanitin-RNA polymerase II cocrystal at 2.8 A resolution.</Title>
-<Xref>DOI:10.1073/pnas.251664698</Xref>
-<Xref>PMID:11805306</Xref>
-<Note>X-ray diffraction with modeled peptide, 2.80 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bushnell, D.A.</Author>
-<Author>Cramer, P.</Author>
-<Author>Kornberg, R.D.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, October 2001</Citation>
-<Description>Crystal structure of yeast RNA polymerase II complexed with the inhibitor alpha amanitin.</Description>
-<Xref>PDB:1K83</Xref>
-<Note>X-ray diffraction with modeled peptide, 2.80 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Brueckner, F.</Author>
-<Author>Cramer, P.</Author>
-</Authors>
-<Citation>Nature Struct. Mol. Biol. 15, 811-818, 2008</Citation>
-<Title>Structural basis of transcription inhibition by alpha-amanitin and implications for RNA polymerase II translocation.</Title>
-<Xref>DOI:10.1038/nsmb.1458</Xref>
-<Xref>PMID:18552824</Xref>
-<Note>X-ray diffraction, 3.40 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Brueckner, F.</Author>
-<Author>Cramer, P.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, May 2008</Citation>
-<Description>Alpha-amanitin inhibited complete RNA polymerase II elongation complex.</Description>
-<Xref>PDB:2VUM</Xref>
-<Note>X-ray diffraction, 3.40 angstroms</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>C, W</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:01380</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__2'-cysteinyl-6'-hydroxytryptophan sulfoxide (trp-cys)__w__c">CROSSLNK 2'-cysteinyl-6'-hydroxytryptophan sulfoxide (Trp-Cys)</Feature>
-</Features>
-<Image src="/images/AA0451.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0451.PDB" />
-</Entry>
-<Entry id="AA0455">
-<Header>
-<Code>AA0455</Code>
-<Dates>
-<CreationDate>08-Aug-2008</CreationDate>
-<StrucRevDate>08-Aug-2008</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-palmitoleoyl-L-serine</Name>
-<AlternateName>L-serine cis-9-hexadecenoate ester</AlternateName>
-<AlternateName>O3-palmitoleoyl-serine</AlternateName>
-<SystematicName>(2S)-2-amino-3-((9Z)-9-hexadecenoyloxy)propanoic acid</SystematicName>
-<Xref>ChEBI:85189</Xref>
-<Xref>PDBHET:PAM</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 19 H 33 N 1 O 3</Formula>
-<Weight type="chemical">323.48</Weight>
-<Weight type="physical">323.246044</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 16 H 28 N 0 O 1</Formula>
-<Weight type="chemical">236.40</Weight>
-<Weight type="physical">236.214016</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Takada, R.</Author>
-<Author>Satomi, Y.</Author>
-<Author>Kurata, T.</Author>
-<Author>Ueno, N.</Author>
-<Author>Norioka, S.</Author>
-<Author>Kondoh, H.</Author>
-<Author>Takao, T.</Author>
-<Author>Takada, S.</Author>
-</Authors>
-<Citation>Dev. Cell 11, 791-801, 2006</Citation>
-<Title>Monounsaturated fatty acid modification of Wnt protein: its role in Wnt secretion.</Title>
-<Xref>DOI:10.1016/j.devcel.2006.10.003</Xref>
-<Xref>PMID:17141155</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Janda, C.Y.</Author>
-<Author>Waghray, D.</Author>
-<Author>Levin, A.M.</Author>
-<Author>Thomas, C.</Author>
-<Author>Garcia, K.C.</Author>
-</Authors>
-<Citation>Science 337, 59-64, 2012</Citation>
-<Title>Structural Basis of Wnt Recognition by Frizzled.</Title>
-<Xref>DOI:10.1126/science.1222879</Xref>
-<Xref>PMID:22653731</Xref>
-<Note>X-ray diffraction, 3.25 angstroms; the modification was produced with Xenopus laevis Wnt8 expressed in Drosophila melanogaster</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Janda, C.Y.</Author>
-<Author>Waghray, D.</Author>
-<Author>Levin, A.M.</Author>
-<Author>Thomas, C.</Author>
-<Author>Garcia, K.C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, May 2012</Citation>
-<Description>Crystal structure of XWnt8 in complex with the cysteine-rich domain of Frizzled 8.</Description>
-<Xref>PDB:4F0A</Xref>
-<Note>X-ray diffraction, 3.25 angstroms; electron density of the lipid is incomplete and the model does not have the expected geometry</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>O-palmitoleoyl transferase</EnzymeName>
-<EnzymeName>(9Z)-hexadec-9-enoyl-CoA:[Wnt]-L-serine O-hexadecenoyltransferase (EC 2.3.1.250)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>PSI-MOD:01381</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lipoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__o-palmitoleyl serine__s">LIPID O-palmitoleyl serine</Feature>
-</Features>
-<Image src="/images/AA0455.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0455.PDB" />
-</Entry>
-<Entry id="AA0456">
-<Header>
-<Code>AA0456</Code>
-<Dates>
-<CreationDate>29-Aug-2008</CreationDate>
-<StrucRevDate>29-Aug-2008</StrucRevDate>
-<TextChngDate>31-May-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N,N,N-trimethyl-L-methionine</Name>
-<AlternateName>(1S)-1-carboxy-N,N,N-trimethyl-3-(methylsulfanyl)propanazanium</AlternateName>
-<AlternateName>2-trimethylammonio-4-(methylthio)butanoic acid</AlternateName>
-<AlternateName>N,N,N-trimethylmethionine cation</AlternateName>
-<AlternateName>N,N,N-trimethylmethioninium</AlternateName>
-<SystematicName>(1S)-1-carboxy-N,N,N-trimethyl-3-(methylsulfanyl)propanaminium</SystematicName>
-<Xref>PDBHET:4MM</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 8 H 17 N 1 O 1 S 1</Formula>
-<FormalCharge>1+</FormalCharge>
-<Weight type="chemical">175.29</Weight>
-<Weight type="physical">175.102537</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0013">
-<Formula>C 3 H 7 N 0 O 0 S 0</Formula>
-<FormalCharge>1+</FormalCharge>
-<Weight type="chemical">43.09</Weight>
-<Weight type="physical">43.054227</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Demirci, H.</Author>
-<Author>Gregory, S.T.</Author>
-<Author>Dahlberg, A.E.</Author>
-<Author>Jogl, G.</Author>
-</Authors>
-<Citation>Structure 16, 1059-1066, 2008</Citation>
-<Title>Multiple-site trimethylation of ribosomal protein L11 by the PrmA methyltransferase.</Title>
-<Xref>DOI:10.1016/j.str.2008.03.016</Xref>
-<Xref>PMID:18611379</Xref>
-<Note>X-ray diffraction, 1.75 angstroms; the model submitted as PDB 3CJU was corrected and replaced by 3EGV</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Demirci, H.</Author>
-<Author>Gregory, S.T.</Author>
-<Author>Dahlberg, A.E.</Author>
-<Author>Jogl, G.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, September 2008</Citation>
-<Description>Ribosomal protein L11 methyltransferase (PrmA) in complex with trimethylated ribosomal protein L11.</Description>
-<Xref>PDB:3EGV</Xref>
-<Note>X-ray diffraction, 1.75 angstroms</Note>
-</ReferenceBlock>
-<Comment>Although appropriate, the keyword "thioether bond" normally does not appear for this amino acid.</Comment>
-<Comment>Consult FAQ at http://pir.georgetown.edu/resid/faq.shtml#q12 concerning calculation of the difference formula.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>ribosomal protein L11 methyltransferase (EC 2.1.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>M</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0018014</Xref>
-<Xref>PSI-MOD:01382</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>*thioether bond</Keyword>
-<Keyword>blocked amino end</Keyword>
-<Keyword>methylated amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n,n,n-trimethylmethionine__m">MOD_RES N,N,N-trimethylmethionine</Feature>
-</Features>
-<Image src="/images/AA0456.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0456.PDB" />
-</Entry>
-<Entry id="AA0457">
-<Header>
-<Code>AA0457</Code>
-<Dates>
-<CreationDate>29-Aug-2008</CreationDate>
-<StrucRevDate>29-Aug-2008</StrucRevDate>
-<TextChngDate>26-Feb-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-cystine S-oxide</Name>
-<AlternateName>cystine sulfoxide</AlternateName>
-<AlternateName>S-cysteinyl 3-(oxidosulfanyl)alanine</AlternateName>
-<AlternateName>S-[(2R)-2-amino-3-oxopropyl] (2R)-2-amino-3-oxopropane-1-sulfinothioate</AlternateName>
-<SystematicName>(2R)-2-amino-3-[([(2R)-2-amino-2-carboxyethyl]sulfanyl)sulfinyl]propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 8 N 2 O 3 S 2</Formula>
-<Weight type="chemical">220.26</Weight>
-<Weight type="physical">219.997634</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005">
-<Formula>C 0 H -2 N 0 O 1 S 0</Formula>
-<Weight type="chemical">13.98</Weight>
-<Weight type="physical">13.979265</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Oke, M.</Author>
-<Author>Ching, R.T.Y.</Author>
-<Author>Carter, L.G.</Author>
-<Author>Johnson, K.A.</Author>
-<Author>Liu, H.</Author>
-<Author>McMahon, S.A.</Author>
-<Author>White, M.F.</Author>
-<Author>Bloch Jr., C.</Author>
-<Author>Botting, C.H.</Author>
-<Author>Walsh, M.A.</Author>
-<Author>Latiff, A.A.</Author>
-<Author>Kennedy, M.W.</Author>
-<Author>Cooper, A.</Author>
-<Author>Naismith, J.H.</Author>
-</Authors>
-<Citation>Angew. Chem. Int. Ed. Engl. 47, 7853-7856, 2008</Citation>
-<Title>Unusual chromophore and cross-links in ranasmurfin: a blue protein from the foam nests of a tropical frog.</Title>
-<Xref>DOI:10.1002/anie.200802901</Xref>
-<Xref>PMID:18781570</Xref>
-<Note>X-ray diffraction, 1.16 angstroms; the authors' names in the PubMed citation are corrected</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Oke, M.</Author>
-<Author>Ching, R.Y.</Author>
-<Author>Carter, L.G.</Author>
-<Author>Johnson, K.A.</Author>
-<Author>Liu, H.</Author>
-<Author>McMahon, S.A.</Author>
-<Author>Bloch Jr., C.</Author>
-<Author>Botting, C.H.</Author>
-<Author>Walsh, M.A.</Author>
-<Author>Latiff, A.A.</Author>
-<Author>Kennedy, M.W.</Author>
-<Author>Cooper, A.</Author>
-<Author>Naismith, J.H.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, November 2007</Citation>
-<Description>Ranasmurfin.</Description>
-<Xref>PDB:2VH3</Xref>
-<Note>X-ray diffraction, 1.16 angstroms</Note>
-</ReferenceBlock>
-<Comment>This modification in the modeled protein has not been chemically confirmed.</Comment>
-<SequenceCode>
-<SequenceSpec>C, C</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:01383</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>disulfide bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__s-cysteinyl 3-(oxidosulfanyl)alanine (cys-cys)__c__c">CROSSLNK S-cysteinyl 3-(oxidosulfanyl)alanine (Cys-Cys)</Feature>
-</Features>
-<Image src="/images/AA0457.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0457.PDB" />
-</Entry>
-<Entry id="AA0458">
-<Header>
-<Code>AA0458</Code>
-<Dates>
-<CreationDate>29-Aug-2008</CreationDate>
-<StrucRevDate>29-Aug-2008</StrucRevDate>
-<TextChngDate>26-Feb-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>aminomalonic acid</Name>
-<AlternateName>2-carboxyglycine</AlternateName>
-<AlternateName>Ama</AlternateName>
-<SystematicName>aminopropanedioic acid</SystematicName>
-<Xref>CAS:1068-84-4</Xref>
-<Xref>PDBHET:FGL</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 3 N 1 O 3</Formula>
-<Weight type="chemical">101.06</Weight>
-<Weight type="physical">101.011293</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 0 H -2 N 0 O 1 S 0</Formula>
-<Weight type="chemical">13.98</Weight>
-<Weight type="physical">13.979265</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Thanassi, J.W.</Author>
-</Authors>
-<Citation>Biochemistry 9, 525-532, 1970</Citation>
-<Title>Aminomalonic acid. Spontaneous decarboxylation and reaction with 5-deoxypyridoxal.</Title>
-<Xref>DOI:10.1021/bi00805a011</Xref>
-<Xref>PMID:5415959</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hauschka, P.V.</Author>
-<Author>Henson, E.B.</Author>
-<Author>Gallop, P.M.</Author>
-</Authors>
-<Citation>Anal. Biochem. 108, 57-63, 1980</Citation>
-<Title>Quantitative analysis and comparative decarboxylation of aminomalonic acid, beta-carboxyaspartic acid, and gamma-carboxyglutamic acid.</Title>
-<Xref>DOI:10.1016/0003-2697(80)90691-0</Xref>
-<Xref>PMID:7457858</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Van Buskirk, J.J.</Author>
-<Author>Kirsch, W.M.</Author>
-<Author>Kleyer, D.L.</Author>
-<Author>Barkley, R.M.</Author>
-<Author>Koch, T.H.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 81, 722-725, 1984</Citation>
-<Title>Aminomalonic acid: identification in Escherichia coli and atherosclerotic plaque.</Title>
-<Xref>DOI:10.1073/pnas.81.3.722</Xref>
-<Xref>PMID:6366787</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Copley, S.D.</Author>
-<Author>Frank, E.</Author>
-<Author>Kirsch, W.M.</Author>
-<Author>Koch, T.H.</Author>
-</Authors>
-<Citation>Anal. Biochem. 201, 152-157, 1992</Citation>
-<Title>Detection and possible origins of aminomalonic acid in protein hydrolysates.</Title>
-<Xref>DOI:10.1016/0003-2697(92)90188-D</Xref>
-<Xref>PMID:1621954</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Oke, M.</Author>
-<Author>Ching, R.T.Y.</Author>
-<Author>Carter, L.G.</Author>
-<Author>Johnson, K.A.</Author>
-<Author>Liu, H.</Author>
-<Author>McMahon, S.A.</Author>
-<Author>White, M.F.</Author>
-<Author>Bloch Jr., C.</Author>
-<Author>Botting, C.H.</Author>
-<Author>Walsh, M.A.</Author>
-<Author>Latiff, A.A.</Author>
-<Author>Kennedy, M.W.</Author>
-<Author>Cooper, A.</Author>
-<Author>Naismith, J.H.</Author>
-</Authors>
-<Citation>Angew. Chem. Int. Ed. Engl. 47, 7853-7856, 2008</Citation>
-<Title>Unusual chromophore and cross-links in ranasmurfin: a blue protein from the foam nests of a tropical frog.</Title>
-<Xref>DOI:10.1002/anie.200802901</Xref>
-<Xref>PMID:18781570</Xref>
-<Note>X-ray diffraction, 1.16 angstroms; the authors' names in the PubMed citation are corrected</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Oke, M.</Author>
-<Author>Ching, R.Y.</Author>
-<Author>Carter, L.G.</Author>
-<Author>Johnson, K.A.</Author>
-<Author>Liu, H.</Author>
-<Author>McMahon, S.A.</Author>
-<Author>Bloch Jr., C.</Author>
-<Author>Botting, C.H.</Author>
-<Author>Walsh, M.A.</Author>
-<Author>Latiff, A.A.</Author>
-<Author>Kennedy, M.W.</Author>
-<Author>Cooper, A.</Author>
-<Author>Naismith, J.H.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, November 2007</Citation>
-<Description>Ranasmurfin.</Description>
-<Xref>PDB:2VH3</Xref>
-<Note>X-ray diffraction, 1.16 angstroms</Note>
-</ReferenceBlock>
-<Comment>This modification in the modeled protein has not been chemically confirmed.</Comment>
-<Comment>As a free amino acid, aminomalonic acid is achiral. However, originating from (2S)-serine in a protein, the residue would be named as a (2R)-2,3-diamino-3-oxopropanoic acid, with the serine carbon-3 carboxyl taking precedence, becoming carbon-1, and changing the stereochemical designation.</Comment>
-<Comment>The PDB Hetgroup FGL was originally designated as the "C(alpha)-formyl glycine" active site residue L-3-oxoalanine (see RESID:AA0185) observed in its hydrated form. That structure, a gem-diol with an sp(3) carbon, was misinterpreted as a carboxyl with an sp(2) carbon and assigned to aminomalonic acid instead.</Comment>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>PSI-MOD:01384</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Features>
-<Feature type="UniProt" key="mod_res__aminomalonic acid (ser)__s">MOD_RES Aminomalonic acid (Ser)</Feature>
-</Features>
-<Image src="/images/AA0458.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0458.PDB" />
-</Entry>
-<Entry id="AA0459">
-<Header>
-<Code>AA0459</Code>
-<Dates>
-<CreationDate>26-Feb-2010</CreationDate>
-<StrucRevDate>26-Feb-2010</StrucRevDate>
-<TextChngDate>29-Oct-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>5'-(L-tyros-5'-yl)amino-L-tyrosine</Name>
-<AlternateName>5'-tyrosyl-5'-aminotyrosine</AlternateName>
-<AlternateName>5'-[(tyros-5'-yl)amino]tyrosine</AlternateName>
-<AlternateName>bis(LTQ) linkage</AlternateName>
-<SystematicName>(2S,2'S)-3,3'-[iminobis(4-hydroxybenzene-3,1-diyl)]bis(2-aminopropanoic acid)</SystematicName>
-<Xref>PDBHET:TY2</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 18 H 17 N 3 O 4</Formula>
-<Weight type="chemical">339.35</Weight>
-<Weight type="physical">339.121906</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0019 AA0019">
-<Formula>C 0 H -1 N 1 O 0</Formula>
-<Weight type="chemical">13.00</Weight>
-<Weight type="physical">12.995249</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Oke, M.</Author>
-<Author>Ching, R.T.Y.</Author>
-<Author>Carter, L.G.</Author>
-<Author>Johnson, K.A.</Author>
-<Author>Liu, H.</Author>
-<Author>McMahon, S.A.</Author>
-<Author>White, M.F.</Author>
-<Author>Bloch Jr., C.</Author>
-<Author>Botting, C.H.</Author>
-<Author>Walsh, M.A.</Author>
-<Author>Latiff, A.A.</Author>
-<Author>Kennedy, M.W.</Author>
-<Author>Cooper, A.</Author>
-<Author>Naismith, J.H.</Author>
-</Authors>
-<Citation>Angew. Chem. Int. Ed. Engl. 47, 7853-7856, 2008</Citation>
-<Title>Unusual chromophore and cross-links in ranasmurfin: a blue protein from the foam nests of a tropical frog.</Title>
-<Xref>DOI:10.1002/anie.200802901</Xref>
-<Xref>PMID:18781570</Xref>
-<Note>X-ray diffraction, 1.16 angstroms; the authors' names in the PubMed citation are corrected</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Oke, M.</Author>
-<Author>Ching, R.Y.</Author>
-<Author>Carter, L.G.</Author>
-<Author>Johnson, K.A.</Author>
-<Author>Liu, H.</Author>
-<Author>McMahon, S.A.</Author>
-<Author>Bloch Jr., C.</Author>
-<Author>Botting, C.H.</Author>
-<Author>Walsh, M.A.</Author>
-<Author>Latiff, A.A.</Author>
-<Author>Kennedy, M.W.</Author>
-<Author>Cooper, A.</Author>
-<Author>Naismith, J.H.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, November 2007</Citation>
-<Description>Ranasmurfin.</Description>
-<Xref>PDB:2VH3</Xref>
-<Note>X-ray diffraction, 1.16 angstroms</Note>
-</ReferenceBlock>
-<Comment>This structure represents the cross-linked tyrosine portion of a four residue bis(lysine tyrosylquinone) structure which is itself part of a zinc binding complex with two histidine residues.</Comment>
-<Comment>This modification in the modeled protein has not been chemically confirmed.</Comment>
-<SequenceCode>
-<SequenceSpec>Y, Y</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Condition>secondary to RESID:AA0233</Condition>
-<Xref>PSI-MOD:01787</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Features>
-<Feature type="UniProt" key="crosslnk__5'-tyrosyl-5'-aminotyrosine (tyr-tyr) (interchain)__y__y">CROSSLNK 5'-tyrosyl-5'-aminotyrosine (Tyr-Tyr) (interchain)</Feature>
-</Features>
-<Image src="/images/AA0459.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0459.PDB" />
-</Entry>
-<Entry id="AA0462">
-<Header>
-<Code>AA0462</Code>
-<Dates>
-<CreationDate>24-Oct-2008</CreationDate>
-<StrucRevDate>24-Oct-2008</StrucRevDate>
-<TextChngDate>26-Feb-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>3-hydroxy-L-phenylalanine</Name>
-<AlternateName>3-hydoxyphenylalanine</AlternateName>
-<AlternateName>3-phenyl-L-serine</AlternateName>
-<AlternateName>beta-hydroxyphenylalanine</AlternateName>
-<AlternateName>beta-phenylserine</AlternateName>
-<AlternateName>L-threo-3-phenylserine</AlternateName>
-<SystematicName>(2S,3S)-2-amino-3-hydroxy-3-phenylpropanoic acid</SystematicName>
-<Xref>CAS:1078-17-7</Xref>
-<Xref>CAS:587-33-7</Xref>
-<Xref>CAS:6254-48-4</Xref>
-<Xref>ChEBI:16795</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 9 N 1 O 2</Formula>
-<Weight type="chemical">163.18</Weight>
-<Weight type="physical">163.063329</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0014">
-<Formula>C 0 H 0 N 0 O 1</Formula>
-<Weight type="chemical">16.00</Weight>
-<Weight type="physical">15.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lin, T.S.</Author>
-<Author>Kolattukudy, P.E.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 106, 341-351, 1980</Citation>
-<Title>Structural studies on cutinase, a glycoprotein containing novel amino acids and glucuronic acid amide at the N terminus.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1980.tb04580.x</Xref>
-<Xref>PMID:7398618</Xref>
-<Note>the location of the modification in the sequence was not determined; all crystallographic determinations have used proteins not expressed in the original species, and thus lacking the modification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kettenring, J.</Author>
-<Author>Colombo, L.</Author>
-<Author>Ferrari, P.</Author>
-<Author>Tavecchia, P.</Author>
-<Author>Nebuloni, M.</Author>
-<Author>Vekey, K.</Author>
-<Author>Gallo, G.G.</Author>
-<Author>Selva, E.</Author>
-</Authors>
-<Citation>J. Antibiot. 44, 702-715, 1991</Citation>
-<Title>Antibiotic GE2270 A: a novel inhibitor of bacterial protein synthesis. II. Structure elucidation.</Title>
-<Xref>PMID:1880060</Xref>
-<Note>mass spectrometric, (1)H-NMR, (13)C-NMR, and IR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Tavecchia, P.</Author>
-<Author>Gentili, P.</Author>
-<Author>Kurz, M.</Author>
-<Author>Sottani, C.</Author>
-<Author>Bonfichi, R.</Author>
-<Author>Lociuro, S.</Author>
-<Author>Selva, E.</Author>
-</Authors>
-<Citation>J. Antibiot. 47, 1564-1567, 1994</Citation>
-<Title>Revised structure of the antibiotic GE 2270A.</Title>
-<Xref>PMID:7844053</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Heffron, S.E.</Author>
-<Author>Jurnak, F.</Author>
-</Authors>
-<Citation>Biochemistry 39, 37-45, 2000</Citation>
-<Title>Structure of an EF-Tu complex with a thiazolyl peptide antibiotic determined at 2.35 A resolution: atomic basis for GE2270A inhibition of EF-Tu.</Title>
-<Xref>DOI:10.1021/bi9913597</Xref>
-<Xref>PMID:10625477</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Heffron, S.E.</Author>
-<Author>Jurnak, F.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, October 1999</Citation>
-<Description>Crystal structure of elongation factor, Tu (EF-Tu-MGGDP) complexed with GE2270A, a thiazolyl peptide antibiotic.</Description>
-<Xref>PDB:1D8T</Xref>
-<Note>X-ray diffraction, 2.35 angstroms; in this low resolution, dimeric structure the modification was modeled as the (2S,3R) diastereomer in one molecule and (2S,3S) in the other</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Heckmann, G.</Author>
-<Author>Bach, T.</Author>
-</Authors>
-<Citation>Angew. Chem. Int. Ed. Engl. 44, 1199-1201, 2005</Citation>
-<Title>Synthesis of the heterocyclic core of the GE 2270 antibiotics and structure elucidation of a major degradation product.</Title>
-<Xref>DOI:10.1002/anie.200461715</Xref>
-<Xref>PMID:15651011</Xref>
-<Note>(1)H-NMR, specific rotation analysis, and chemical synthesis; establishes that the modification is the (2S,3S) diastereomer</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Parmeggiani, A.</Author>
-<Author>Krab, I.M.</Author>
-<Author>Okamura, S.</Author>
-<Author>Nielsen, R.C.</Author>
-<Author>Nyborg, J.</Author>
-<Author>Nissen, P.</Author>
-</Authors>
-<Citation>Biochemistry 45, 6846-6857, 2006</Citation>
-<Title>Structural basis of the action of pulvomycin and GE2270 A on elongation factor Tu.</Title>
-<Xref>DOI:10.1021/bi0525122</Xref>
-<Xref>PMID:16734421</Xref>
-<Note>X-ray diffraction, 1.60 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Parmeggiani, A.</Author>
-<Author>Krab, I.M.</Author>
-<Author>Okamura, S.</Author>
-<Author>Nielsen, R.C.</Author>
-<Author>Nyborg, J.</Author>
-<Author>Nissen, P.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, November 2005</Citation>
-<Description>EF-Tu complexed with a GTP analog and the antibiotic GE2270 A.</Description>
-<Xref>PDB:2C77</Xref>
-<Note>X-ray diffraction, 1.60 angstroms</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>F</SequenceSpec>
-<Xref>PSI-MOD:01385</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__3-hydroxyphenylalanine__f">MOD_RES 3-hydroxyphenylalanine</Feature>
-</Features>
-<Image src="/images/AA0462.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0462.PDB" />
-</Entry>
-<Entry id="AA0463">
-<Header>
-<Code>AA0463</Code>
-<Dates>
-<CreationDate>24-Oct-2008</CreationDate>
-<StrucRevDate>24-Oct-2008</StrucRevDate>
-<TextChngDate>30-Jan-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>3-hydroxy-L-valine</Name>
-<AlternateName>3-hydroxyvaline</AlternateName>
-<SystematicName>(2S)-2-amino-3-hydroxy-3-methylbutanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 9 N 1 O 2</Formula>
-<Weight type="chemical">115.13</Weight>
-<Weight type="physical">115.063329</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0020">
-<Formula>C 0 H 0 N 0 O 1</Formula>
-<Weight type="chemical">16.00</Weight>
-<Weight type="physical">15.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Shoji, J.</Author>
-<Author>Kato, T.</Author>
-<Author>Yoshimura, Y.</Author>
-<Author>Tori, K.</Author>
-</Authors>
-<Citation>J. Antibiot. 34, 1126-1136, 1981</Citation>
-<Title>Structural studies on thiocillins I, II and III (studies on antibiotics from the genus Bacillus XXIX).</Title>
-<Xref>PMID:7328054</Xref>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>V</SequenceSpec>
-<Xref>PSI-MOD:01386</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__3-hydroxyvaline__v">MOD_RES 3-hydroxyvaline</Feature>
-</Features>
-<Image src="/images/AA0463.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0463.PDB" />
-</Entry>
-<Entry id="AA0464">
-<Header>
-<Code>AA0464</Code>
-<Dates>
-<CreationDate>24-Oct-2008</CreationDate>
-<StrucRevDate>24-Oct-2008</StrucRevDate>
-<TextChngDate>31-Dec-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-methyl-L-threonine</Name>
-<AlternateName>O-methyl threonine</AlternateName>
-<AlternateName>threonine methyl ether</AlternateName>
-<SystematicName>(2S,3R)-2-amino-3-methoxybutanoic acid</SystematicName>
-<Xref>CAS:4385-90-4</Xref>
-<Xref>PDBHET:OLT</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 9 N 1 O 2</Formula>
-<Weight type="chemical">115.13</Weight>
-<Weight type="physical">115.063329</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0017">
-<Formula>C 1 H 2 N 0 O 0</Formula>
-<Weight type="chemical">14.03</Weight>
-<Weight type="physical">14.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Shoji, J.</Author>
-<Author>Kato, T.</Author>
-<Author>Yoshimura, Y.</Author>
-<Author>Tori, K.</Author>
-</Authors>
-<Citation>J. Antibiot. 34, 1126-1136, 1981</Citation>
-<Title>Structural studies on thiocillins I, II and III (studies on antibiotics from the genus Bacillus XXIX).</Title>
-<Xref>PMID:7328054</Xref>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>T</SequenceSpec>
-<Condition>incidental to RESID:AA0483</Condition>
-<Xref>PSI-MOD:01387</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>methylated amino acid</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__o-methylthreonine__t">MOD_RES O-methylthreonine</Feature>
-</Features>
-<Image src="/images/AA0464.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0464.PDB" />
-</Entry>
-<Entry id="AA0465">
-<Header>
-<Code>AA0465</Code>
-<Dates>
-<CreationDate>24-Oct-2008</CreationDate>
-<StrucRevDate>24-Oct-2008</StrucRevDate>
-<TextChngDate>30-Jan-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>1-amino-2-propanol</Name>
-<AlternateName>1-amino-2-hydroxypropane</AlternateName>
-<AlternateName>1-methyl-2-aminoethanol</AlternateName>
-<AlternateName>2-amino-1-methylethanol</AlternateName>
-<AlternateName>2-hydroxy-1-propylamine</AlternateName>
-<AlternateName>2-hydroxypropanamine</AlternateName>
-<AlternateName>2-hydroxypropylamine</AlternateName>
-<AlternateName>alpha-aminoisopropyl alcohol</AlternateName>
-<AlternateName>decarboxylated threonine</AlternateName>
-<AlternateName>isopropanolamine</AlternateName>
-<AlternateName>threamine</AlternateName>
-<SystematicName>(2R)-1-aminopropan-2-ol</SystematicName>
-<Xref>CAS:35320-23-1</Xref>
-<Xref>ChEBI:15675</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 8 N 1 O 1</Formula>
-<Weight type="chemical">74.10</Weight>
-<Weight type="physical">74.060589</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0017">
-<Formula>C -1 H 0 N 0 O -2</Formula>
-<Weight type="chemical">-44.01</Weight>
-<Weight type="physical">-43.989829</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Shoji, J.</Author>
-<Author>Kato, T.</Author>
-<Author>Yoshimura, Y.</Author>
-<Author>Tori, K.</Author>
-</Authors>
-<Citation>J. Antibiot. 34, 1126-1136, 1981</Citation>
-<Title>Structural studies on thiocillins I, II and III (studies on antibiotics from the genus Bacillus XXIX).</Title>
-<Xref>PMID:7328054</Xref>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>T</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>PSI-MOD:01388</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__decarboxylated threonine__t">MOD_RES Decarboxylated threonine</Feature>
-</Features>
-<Image src="/images/AA0465.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0465.PDB" />
-</Entry>
-<Entry id="AA0466">
-<Header>
-<Code>AA0466</Code>
-<Dates>
-<CreationDate>24-Oct-2008</CreationDate>
-<StrucRevDate>24-Oct-2008</StrucRevDate>
-<TextChngDate>30-Sep-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-isoleucine thiazole-4-carboxylic acid</Name>
-<AlternateName>2-[1-zanyl-2-methylbutyl]-1,3-thiazole-4-carboxylic acid</AlternateName>
-<SystematicName>2-[(1S,2S)-1-amino-2-methylbutyl]-1,3-thiazole-4-carboxylic acid</SystematicName>
-<Xref>PDBHET:BB9</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 12 N 2 O 1 S 1</Formula>
-<Weight type="chemical">196.27</Weight>
-<Weight type="physical">196.067034</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0010">
-<Formula>C 0 H -4 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-20.03</Weight>
-<Weight type="physical">-20.026215</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bond, C.S.</Author>
-<Author>Shaw, M.P.</Author>
-<Author>Alphey, M.S.</Author>
-<Author>Hunter, W.N.</Author>
-</Authors>
-<Citation>Acta Crystallogr. D Biol. Crystallogr. 57, 755-758, 2001</Citation>
-<Title>Structure of the macrocycle thiostrepton solved using the anomalous dispersion contribution of sulfur.</Title>
-<Xref>DOI:10.1107/S0907444901003134</Xref>
-<Xref>PMID:11320328</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bond, C.S.</Author>
-<Author>Shaw, M.P.</Author>
-<Author>Alphey, M.S.</Author>
-<Author>Hunter, W.N.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, October 2000</Citation>
-<Description>Structure of the macrocycle thiostrepton solved using the anomalous dispersion contribution of sulfur.</Description>
-<Xref>PDB:1E9W</Xref>
-<Note>X-ray diffraction, 1.02 angstroms</Note>
-</ReferenceBlock>
-<Comment>Formed by the condensation of a cysteine thiol with the carbonyl of the preceding residue and alpha-beta dehydrogenation.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptidyl-cysteine cyclase (EC 4.2.1.-)</EnzymeName>
-<EnzymeName>peptidyl-thiazoline dehydrogenase (EC 1.3.-.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C, I</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Xref>PSI-MOD:01389</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>oxazole/thiazole ring</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__thiazole-4-carboxylic acid (ile-cys)__i__c">CROSSLNK Thiazole-4-carboxylic acid (Ile-Cys)</Feature>
-</Features>
-<Image src="/images/AA0466.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0466.PDB" />
-</Entry>
-<Entry id="AA0467">
-<Header>
-<Code>AA0467</Code>
-<Dates>
-<CreationDate>24-Oct-2008</CreationDate>
-<StrucRevDate>24-Oct-2008</StrucRevDate>
-<TextChngDate>30-Sep-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-valine thiazole-4-carboxylic acid</Name>
-<AlternateName>2-[1-azanyl-2-methylpropyl]-1,3-thiazole-4-carboxylic acid</AlternateName>
-<SystematicName>2-[(1S)-1-amino-2-methylpropyl]-1,3-thiazole-4-carboxylic acid</SystematicName>
-<Xref>PDBHET:BB9</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 8 H 10 N 2 O 1 S 1</Formula>
-<Weight type="chemical">182.24</Weight>
-<Weight type="physical">182.051384</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0020">
-<Formula>C 0 H -4 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-20.03</Weight>
-<Weight type="physical">-20.026215</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Shoji, J.</Author>
-<Author>Kato, T.</Author>
-<Author>Yoshimura, Y.</Author>
-<Author>Tori, K.</Author>
-</Authors>
-<Citation>J. Antibiot. 34, 1126-1136, 1981</Citation>
-<Title>Structural studies on thiocillins I, II and III (studies on antibiotics from the genus Bacillus XXIX).</Title>
-<Xref>PMID:7328054</Xref>
-</ReferenceBlock>
-<Comment>Formed by the condensation of a cysteine thiol with the carbonyl of the preceding residue and alpha-beta dehydrogenation.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptidyl-cysteine cyclase (EC 4.2.1.-)</EnzymeName>
-<EnzymeName>peptidyl-thiazoline dehydrogenase (EC 1.3.-.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C, V</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Xref>PSI-MOD:01390</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>oxazole/thiazole ring</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__thiazole-4-carboxylic acid (val-cys)__v__c">CROSSLNK Thiazole-4-carboxylic acid (Val-Cys)</Feature>
-</Features>
-<Image src="/images/AA0467.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0467.PDB" />
-</Entry>
-<Entry id="AA0468">
-<Header>
-<Code>AA0468</Code>
-<Dates>
-<CreationDate>24-Oct-2008</CreationDate>
-<StrucRevDate>30-Jan-2009</StrucRevDate>
-<TextChngDate>25-Feb-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-valine 5-(methoxymethyl)thiazole-4-carboxylic acid</Name>
-<AlternateName>2-[1-azanyl-2-methylpropyl]-5-(methoxymethyl)-1,3-thiazole-4-carboxylic acid</AlternateName>
-<SystematicName>2-[(1S)-1-amino-2-methylpropyl]-5-(methoxymethyl)-1,3-thiazole-4-carboxylic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 10 H 14 N 2 O 2 S 1</Formula>
-<Weight type="chemical">226.29</Weight>
-<Weight type="physical">226.077599</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0020">
-<Formula>C 2 H 0 N 0 O 0 S 0</Formula>
-<Weight type="chemical">24.02</Weight>
-<Weight type="physical">24.000000</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kettenring, J.</Author>
-<Author>Colombo, L.</Author>
-<Author>Ferrari, P.</Author>
-<Author>Tavecchia, P.</Author>
-<Author>Nebuloni, M.</Author>
-<Author>Vekey, K.</Author>
-<Author>Gallo, G.G.</Author>
-<Author>Selva, E.</Author>
-</Authors>
-<Citation>J. Antibiot. 44, 702-715, 1991</Citation>
-<Title>Antibiotic GE2270 A: a novel inhibitor of bacterial protein synthesis. II. Structure elucidation.</Title>
-<Xref>PMID:1880060</Xref>
-<Note>mass spectrometric, (1)H-NMR, (13)C-NMR, and IR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Tavecchia, P.</Author>
-<Author>Gentili, P.</Author>
-<Author>Kurz, M.</Author>
-<Author>Sottani, C.</Author>
-<Author>Bonfichi, R.</Author>
-<Author>Lociuro, S.</Author>
-<Author>Selva, E.</Author>
-</Authors>
-<Citation>J. Antibiot. 47, 1564-1567, 1994</Citation>
-<Title>Revised structure of the antibiotic GE 2270A.</Title>
-<Xref>PMID:7844053</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Heffron, S.E.</Author>
-<Author>Jurnak, F.</Author>
-</Authors>
-<Citation>Biochemistry 39, 37-45, 2000</Citation>
-<Title>Structure of an EF-Tu complex with a thiazolyl peptide antibiotic determined at 2.35 A resolution: atomic basis for GE2270A inhibition of EF-Tu.</Title>
-<Xref>DOI:10.1021/bi9913597</Xref>
-<Xref>PMID:10625477</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Heffron, S.E.</Author>
-<Author>Jurnak, F.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, October 1999</Citation>
-<Description>Crystal structure of elongation factor, Tu (EF-Tu-MGGDP) complexed with GE2270A, a thiazolyl peptide antibiotic.</Description>
-<Xref>PDB:1D8T</Xref>
-<Note>X-ray diffraction, 2.35 angstroms</Note>
-</ReferenceBlock>
-<Comment>Formed by the condensation of a cysteine thiol with the carbonyl of the preceding residue and alpha-beta dehydrogenation.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptidyl-cysteine cyclase (EC 4.2.1.-)</EnzymeName>
-<EnzymeName>peptidyl-thiazoline dehydrogenase (EC 1.3.-.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C, V</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Xref>PSI-MOD:01391</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>methylated amino acid</Keyword>
-<Keyword>oxazole/thiazole ring</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__5-(methoxymethyl)thiazole-4-carboxylic acid (val-cys)__v__c">CROSSLNK 5-(methoxymethyl)thiazole-4-carboxylic acid (Val-Cys)</Feature>
-</Features>
-<Image src="/images/AA0468.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0468.PDB" />
-</Entry>
-<Entry id="AA0469">
-<Header>
-<Code>AA0469</Code>
-<Dates>
-<CreationDate>24-Oct-2008</CreationDate>
-<StrucRevDate>24-Oct-2008</StrucRevDate>
-<TextChngDate>25-Feb-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-asparagine 5-methylthiazole-4-carboxylic acid</Name>
-<AlternateName>2-[(1S)-1,3-bisazanyl-3-oxopropyl]-5-methyl-1,3-thiazole-4-carboxylic acid</AlternateName>
-<SystematicName>2-[(1S)-1,3-diamino-3-oxopropyl]-5-methyl-1,3-thiazole-4-carboxylic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 8 H 9 N 3 O 2 S 1</Formula>
-<Weight type="chemical">211.24</Weight>
-<Weight type="physical">211.041548</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0003 AA0005">
-<Formula>C 1 H -2 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-6.00</Weight>
-<Weight type="physical">-6.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kettenring, J.</Author>
-<Author>Colombo, L.</Author>
-<Author>Ferrari, P.</Author>
-<Author>Tavecchia, P.</Author>
-<Author>Nebuloni, M.</Author>
-<Author>Vekey, K.</Author>
-<Author>Gallo, G.G.</Author>
-<Author>Selva, E.</Author>
-</Authors>
-<Citation>J. Antibiot. 44, 702-715, 1991</Citation>
-<Title>Antibiotic GE2270 A: a novel inhibitor of bacterial protein synthesis. II. Structure elucidation.</Title>
-<Xref>PMID:1880060</Xref>
-<Note>mass spectrometric, (1)H-NMR, (13)C-NMR, and IR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Tavecchia, P.</Author>
-<Author>Gentili, P.</Author>
-<Author>Kurz, M.</Author>
-<Author>Sottani, C.</Author>
-<Author>Bonfichi, R.</Author>
-<Author>Lociuro, S.</Author>
-<Author>Selva, E.</Author>
-</Authors>
-<Citation>J. Antibiot. 47, 1564-1567, 1994</Citation>
-<Title>Revised structure of the antibiotic GE 2270A.</Title>
-<Xref>PMID:7844053</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Heffron, S.E.</Author>
-<Author>Jurnak, F.</Author>
-</Authors>
-<Citation>Biochemistry 39, 37-45, 2000</Citation>
-<Title>Structure of an EF-Tu complex with a thiazolyl peptide antibiotic determined at 2.35 A resolution: atomic basis for GE2270A inhibition of EF-Tu.</Title>
-<Xref>DOI:10.1021/bi9913597</Xref>
-<Xref>PMID:10625477</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Heffron, S.E.</Author>
-<Author>Jurnak, F.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, October 1999</Citation>
-<Description>Crystal structure of elongation factor, Tu (EF-Tu-MGGDP) complexed with GE2270A, a thiazolyl peptide antibiotic.</Description>
-<Xref>PDB:1D8T</Xref>
-<Note>X-ray diffraction, 2.35 angstroms</Note>
-</ReferenceBlock>
-<Comment>Formed by the condensation of a cysteine thiol with the carbonyl of the preceding residue and alpha-beta dehydrogenation.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptidyl-cysteine cyclase (EC 4.2.1.-)</EnzymeName>
-<EnzymeName>peptidyl-thiazoline dehydrogenase (EC 1.3.-.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C, N</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Xref>PSI-MOD:01392</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>methylated amino acid</Keyword>
-<Keyword>oxazole/thiazole ring</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__5-methylthiazole-4-carboxylic acid (asn-cys)__n__c">CROSSLNK 5-methylthiazole-4-carboxylic acid (Asn-Cys)</Feature>
-</Features>
-<Image src="/images/AA0469.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0469.PDB" />
-</Entry>
-<Entry id="AA0470">
-<Header>
-<Code>AA0470</Code>
-<Dates>
-<CreationDate>24-Oct-2008</CreationDate>
-<StrucRevDate>24-Oct-2008</StrucRevDate>
-<TextChngDate>29-Nov-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-cysteine pyridine-2,5-dicarboxylic acid</Name>
-<SystematicName>6-[(1R)-1-amino-2-sulfanylethyl]pyridine-2,5-dicarboxylic acid</SystematicName>
-<Xref>PDBHET:GEA</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 7 N 2 O 2 S 1</Formula>
-<Weight type="chemical">207.23</Weight>
-<Weight type="physical">207.022823</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0016 AA0016">
-<Formula>C 0 H -8 N -1 O -3 S 0</Formula>
-<Weight type="chemical">-70.07</Weight>
-<Weight type="physical">-70.050418</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kettenring, J.</Author>
-<Author>Colombo, L.</Author>
-<Author>Ferrari, P.</Author>
-<Author>Tavecchia, P.</Author>
-<Author>Nebuloni, M.</Author>
-<Author>Vekey, K.</Author>
-<Author>Gallo, G.G.</Author>
-<Author>Selva, E.</Author>
-</Authors>
-<Citation>J. Antibiot. 44, 702-715, 1991</Citation>
-<Title>Antibiotic GE2270 A: a novel inhibitor of bacterial protein synthesis. II. Structure elucidation.</Title>
-<Xref>PMID:1880060</Xref>
-<Note>mass spectrometric, (1)H-NMR, (13)C-NMR, and IR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Tavecchia, P.</Author>
-<Author>Gentili, P.</Author>
-<Author>Kurz, M.</Author>
-<Author>Sottani, C.</Author>
-<Author>Bonfichi, R.</Author>
-<Author>Lociuro, S.</Author>
-<Author>Selva, E.</Author>
-</Authors>
-<Citation>J. Antibiot. 47, 1564-1567, 1994</Citation>
-<Title>Revised structure of the antibiotic GE 2270A.</Title>
-<Xref>PMID:7844053</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Heffron, S.E.</Author>
-<Author>Jurnak, F.</Author>
-</Authors>
-<Citation>Biochemistry 39, 37-45, 2000</Citation>
-<Title>Structure of an EF-Tu complex with a thiazolyl peptide antibiotic determined at 2.35 A resolution: atomic basis for GE2270A inhibition of EF-Tu.</Title>
-<Xref>DOI:10.1021/bi9913597</Xref>
-<Xref>PMID:10625477</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Heffron, S.E.</Author>
-<Author>Jurnak, F.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, October 1999</Citation>
-<Description>Crystal structure of elongation factor, Tu (EF-Tu-MGGDP) complexed with GE2270A, a thiazolyl peptide antibiotic.</Description>
-<Xref>PDB:1D8T</Xref>
-<Note>X-ray diffraction, 2.35 angstroms</Note>
-</ReferenceBlock>
-<Comment>Formed by the metathesis of two didehydroalanines made from serines, condensation with a cysteine carbonyl and dehydrogenation.</Comment>
-<Comment>This modification is currently represented in the PDB as part of the HET group for the entire molecule of antibiotic GE2270 A.</Comment>
-<SequenceCode>
-<SequenceSpec>C, S, S</SequenceSpec>
-<Condition>cross-link 3</Condition>
-<Condition>incidental to RESID:AA0244</Condition>
-<Xref>PSI-MOD:01393</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>pyridine ring</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__pyridine-2,5-dicarboxylic acid (ser-ser) (with c-__s__s">CROSSLNK Pyridine-2,5-dicarboxylic acid (Ser-Ser) (with C-...)</Feature>
-<Feature type="UniProt" key="crosslnk__pyridine-2,5-dicarboxylic acid (ser-cys) (with s-__s__c">CROSSLNK Pyridine-2,5-dicarboxylic acid (Ser-Cys) (with S-...)</Feature>
-</Features>
-<Image src="/images/AA0470.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0470.PDB" />
-</Entry>
-<Entry id="AA0471">
-<Header>
-<Code>AA0471</Code>
-<Dates>
-<CreationDate>24-Oct-2008</CreationDate>
-<StrucRevDate>24-Oct-2008</StrucRevDate>
-<TextChngDate>30-Jun-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-cysteine 5-amino-3,4,5,6-tetrahydropyridine-2,5-dicarboxylic acid</Name>
-<AlternateName>L-cysteine 5-aminopiperideine-2,5-dicarboxylic acid</AlternateName>
-<SystematicName>(5R,6R)-5-amino-6-[(1R)-1-amino-2-sulfanylethyl]-3,4,5,6-tetrahydropyridine-2,5-dicarboxylic acid</SystematicName>
-<Xref>PDBHET:XBB</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 11 N 3 O 2 S 1</Formula>
-<Weight type="chemical">225.27</Weight>
-<Weight type="physical">225.057198</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0016 AA0016">
-<Formula>C 0 H -5 N 0 O -3 S 0</Formula>
-<Weight type="chemical">-53.04</Weight>
-<Weight type="physical">-53.023869</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bond, C.S.</Author>
-<Author>Shaw, M.P.</Author>
-<Author>Alphey, M.S.</Author>
-<Author>Hunter, W.N.</Author>
-</Authors>
-<Citation>Acta Crystallogr. D Biol. Crystallogr. 57, 755-758, 2001</Citation>
-<Title>Structure of the macrocycle thiostrepton solved using the anomalous dispersion contribution of sulfur.</Title>
-<Xref>DOI:10.1107/S0907444901003134</Xref>
-<Xref>PMID:11320328</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bond, C.S.</Author>
-<Author>Shaw, M.P.</Author>
-<Author>Alphey, M.S.</Author>
-<Author>Hunter, W.N.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, October 2000</Citation>
-<Description>Structure of the macrocycle thiostrepton solved using the anomalous dispersion contribution of sulfur.</Description>
-<Xref>PDB:1E9W</Xref>
-<Note>X-ray diffraction, 1.02 angstroms</Note>
-</ReferenceBlock>
-<Comment>Formed by the metathesis of two didehydroalanines made from serines, condensation with a cysteine carbonyl and dehydrogenation.</Comment>
-<SequenceCode>
-<SequenceSpec>C, S, S</SequenceSpec>
-<Condition>cross-link 3</Condition>
-<Condition>amino-terminal</Condition>
-<Condition>incidental to RESID:AA0244</Condition>
-<Xref>PSI-MOD:01394</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-<Keyword>pyridine ring</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__5-amino-piperideine-2,5-dicarboxylic acid (ser-cys) (with s-__s__c">CROSSLNK 5-amino-piperideine-2,5-dicarboxylic acid (Ser-Cys) (with S-...)</Feature>
-<Feature type="UniProt" key="crosslnk__5-amino-piperideine-2,5-dicarboxylic acid (ser-ser) (with c-__s__s">CROSSLNK 5-amino-piperideine-2,5-dicarboxylic acid (Ser-Ser) (with C-...)</Feature>
-</Features>
-<Image src="/images/AA0471.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0471.PDB" />
-</Entry>
-<Entry id="AA0472">
-<Header>
-<Code>AA0472</Code>
-<Dates>
-<CreationDate>24-Oct-2008</CreationDate>
-<StrucRevDate>24-Oct-2008</StrucRevDate>
-<TextChngDate>28-Oct-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>4-(1-hydroxyethyl)-7-isoleucino-2-(threonin-O3-ylcarbonyl)-7,8-dihydroquinolin-8-ol</Name>
-<SystematicName>(7R,8S)-7-[(1S,2S)-1-carboxy-2-methylbutyl]amino-2-([(1S,2R)-1-amino-1-carboxypropan-2-yl]oxy)carbonyl-8-hydroxy-4-[(1S)-1-hydroxyethyl]-7,8-dihydroquinoline</SystematicName>
-<Xref>PDBHET:QUA</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 22 H 28 N 3 O 6</Formula>
-<Weight type="chemical">430.48</Weight>
-<Weight type="physical">430.197811</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0010 AA0017">
-<Formula>C 12 H 9 N 1 O 3</Formula>
-<Weight type="chemical">215.21</Weight>
-<Weight type="physical">215.058243</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bond, C.S.</Author>
-<Author>Shaw, M.P.</Author>
-<Author>Alphey, M.S.</Author>
-<Author>Hunter, W.N.</Author>
-</Authors>
-<Citation>Acta Crystallogr. D Biol. Crystallogr. 57, 755-758, 2001</Citation>
-<Title>Structure of the macrocycle thiostrepton solved using the anomalous dispersion contribution of sulfur.</Title>
-<Xref>DOI:10.1107/S0907444901003134</Xref>
-<Xref>PMID:11320328</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bond, C.S.</Author>
-<Author>Shaw, M.P.</Author>
-<Author>Alphey, M.S.</Author>
-<Author>Hunter, W.N.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, October 2000</Citation>
-<Description>Structure of the macrocycle thiostrepton solved using the anomalous dispersion contribution of sulfur.</Description>
-<Xref>PDB:1E9W</Xref>
-<Note>X-ray diffraction, 1.02 angstroms</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>I, T</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:01395</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="binding__4-(1-hydroxyethyl)-7,8-dihydroquinolin-8-ol (covalent; via 2 links)">BINDING 4-(1-hydroxyethyl)-7,8-dihydroquinolin-8-ol (covalent; via 2 links)</Feature>
-</Features>
-<Image src="/images/AA0472.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0472.PDB" />
-</Entry>
-<Entry id="AA0473">
-<Header>
-<Code>AA0473</Code>
-<Dates>
-<CreationDate>05-Dec-2008</CreationDate>
-<StrucRevDate>05-Dec-2008</StrucRevDate>
-<TextChngDate>28-Oct-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>5-hydroxy-3-methyl-L-proline</Name>
-<AlternateName>5-hydroxy-3-methylproline</AlternateName>
-<AlternateName>beta-methyl-delta-hydroxyproline</AlternateName>
-<SystematicName>(2S,3S,5Xi)-5-hydroxy-3-methylpyrrolidine-2-carboxylic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 9 N 1 O 2</Formula>
-<Weight type="chemical">127.14</Weight>
-<Weight type="physical">127.063329</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0010">
-<Formula>C 0 H -2 N 0 O 1</Formula>
-<Weight type="chemical">13.98</Weight>
-<Weight type="physical">13.979265</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Stella, S.</Author>
-<Author>Montanini, N.</Author>
-<Author>Le Monnier, F.</Author>
-<Author>Ferrari, P.</Author>
-<Author>Colombo, L.</Author>
-<Author>Marinelli, F.</Author>
-<Author>Landini, P.</Author>
-<Author>Ciciliato, I.</Author>
-<Author>Goldstein, B.P.</Author>
-<Author>Selva, E.</Author>
-</Authors>
-<Citation>J. Antibiot. 48, 780-786, 1995</Citation>
-<Title>Antibiotic GE37468 A: a new inhibitor of bacterial protein synthesis. I. Isolation and characterization.</Title>
-<Xref>PMID:7592021</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ferrari, P.</Author>
-<Author>Colombo, L.</Author>
-<Author>Stella, S.</Author>
-<Author>Selva, E.</Author>
-<Author>Zerilli, L.F.</Author>
-</Authors>
-<Citation>J. Antibiot. 48, 1304-1311, 1995</Citation>
-<Title>Antibiotic GE37468 A: a novel inhibitor of bacterial protein synthesis. II. Structure elucidation.</Title>
-<Xref>PMID:8557573</Xref>
-<Note>mass spectrometric, (1)H-NMR and (13)C-NMR analysis; chemical characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Young, T.S.</Author>
-<Author>Walsh, C.T.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 108, 13053-13058, 2011</Citation>
-<Title>Identification of the thiazolyl peptide GE37468 gene cluster from Streptomyces ATCC 55365 and heterologous expression in Streptomyces lividans.</Title>
-<Xref>DOI:10.1073/pnas.1110435108</Xref>
-<Xref>PMID:21788474</Xref>
-<Note>gene sequence for the encoded peptide; mass spectrometric identification, isotope labeling and (1)H-NMR identification; biosynthesis</Note>
-</ReferenceBlock>
-<Comment>The stereochemistry at C3 and C5 has not been resolved, but (3S) can be assumed by derivation from L-isoleucine. The (3S,5S) form is shown.</Comment>
-<SequenceCode>
-<SequenceSpec>L</SequenceSpec>
-<Xref>PSI-MOD:01897</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__5-hydroxy-3-methylproline (ile)__i">MOD_RES 5-hydroxy-3-methylproline (Ile)</Feature>
-</Features>
-<Image src="/images/AA0473.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0473.PDB" />
-</Entry>
-<Entry id="AA0474">
-<Header>
-<Code>AA0474</Code>
-<Dates>
-<CreationDate>05-Dec-2008</CreationDate>
-<StrucRevDate>05-Dec-2008</StrucRevDate>
-<TextChngDate>25-Feb-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-serine 5-methyloxazole-4-carboxylic acid</Name>
-<AlternateName>2-[1-azanyl-2-hydroxyethyl]-5-methyl-1,3-oxazole-4-carboxylic acid</AlternateName>
-<SystematicName>2-[(1S)-1-amino-2-hydroxyethyl]-5-methyl-1,3-oxazole-4-carboxylic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 8 N 2 O 3</Formula>
-<Weight type="chemical">168.15</Weight>
-<Weight type="physical">168.053492</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016 AA0017">
-<Formula>C 0 H -4 N 0 O -1</Formula>
-<Weight type="chemical">-20.03</Weight>
-<Weight type="physical">-20.026215</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Stella, S.</Author>
-<Author>Montanini, N.</Author>
-<Author>Le Monnier, F.</Author>
-<Author>Ferrari, P.</Author>
-<Author>Colombo, L.</Author>
-<Author>Marinelli, F.</Author>
-<Author>Landini, P.</Author>
-<Author>Ciciliato, I.</Author>
-<Author>Goldstein, B.P.</Author>
-<Author>Selva, E.</Author>
-</Authors>
-<Citation>J. Antibiot. 48, 780-786, 1995</Citation>
-<Title>Antibiotic GE37468 A: a new inhibitor of bacterial protein synthesis. I. Isolation and characterization.</Title>
-<Xref>PMID:7592021</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ferrari, P.</Author>
-<Author>Colombo, L.</Author>
-<Author>Stella, S.</Author>
-<Author>Selva, E.</Author>
-<Author>Zerilli, L.F.</Author>
-</Authors>
-<Citation>J. Antibiot. 48, 1304-1311, 1995</Citation>
-<Title>Antibiotic GE37468 A: a novel inhibitor of bacterial protein synthesis. II. Structure elucidation.</Title>
-<Xref>PMID:8557573</Xref>
-<Note>mass spectrometric, (1)H-NMR and (13)C-NMR analysis; chemical characterization</Note>
-</ReferenceBlock>
-<Comment>Formed by the condensation of a threonine hydroxyl with the carbonyl of the preceding residue and alpha-beta dehydrogenation.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptidyl-threonine cyclase (EC 4.2.1.-)</EnzymeName>
-<EnzymeName>peptidyl-oxazoline dehydrogenase (EC 1.3.-.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>S, T</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Xref>PSI-MOD:01397</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>oxazole/thiazole ring</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__5-methyloxazole-4-carboxylic acid (ser-thr)__s__t">CROSSLNK 5-methyloxazole-4-carboxylic acid (Ser-Thr)</Feature>
-</Features>
-<Image src="/images/AA0474.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0474.PDB" />
-</Entry>
-<Entry id="AA0475">
-<Header>
-<Code>AA0475</Code>
-<Dates>
-<CreationDate>05-Dec-2008</CreationDate>
-<StrucRevDate>05-Dec-2008</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6-propanoyl-L-lysine</Name>
-<AlternateName>2-amino-6-propionylaminocaproic acid</AlternateName>
-<AlternateName>epsilon-propanoyl-L-lysine</AlternateName>
-<AlternateName>epsilon-propionyl-L-lysine</AlternateName>
-<AlternateName>N(zeta)-propanoyllysine</AlternateName>
-<AlternateName>N6-(1-oxopropyl)-L-lysine</AlternateName>
-<AlternateName>N6-propionyllysine</AlternateName>
-<SystematicName>(2S)-2-amino-6-(propanoylamino)hexanoic acid</SystematicName>
-<Xref>CAS:1974-17-0</Xref>
-<Xref>PDBHET:PRK</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 16 N 2 O 2</Formula>
-<Weight type="chemical">184.24</Weight>
-<Weight type="physical">184.121178</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 3 H 4 N 0 O 1</Formula>
-<Weight type="chemical">56.06</Weight>
-<Weight type="physical">56.026215</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kawai, Y.</Author>
-<Author>Fujii, H.</Author>
-<Author>Okada, M.</Author>
-<Author>Tsuchie, Y.</Author>
-<Author>Uchida, K.</Author>
-<Author>Osawa, T.</Author>
-</Authors>
-<Citation>J. Lipid Res. 47, 1386-1398, 2006</Citation>
-<Title>Formation of Nepsilon-(succinyl)lysine in vivo: a novel marker for docosahexaenoic acid-derived protein modification.</Title>
-<Xref>DOI:10.1194/jlr.M600091-JLR200</Xref>
-<Xref>PMID:16582421</Xref>
-<Note>chromatographic detection; mass spectrometric identification; a major product after radical-catalyzed peroxidation of docosahexaenoic acid</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Chen, Y.</Author>
-<Author>Sprung, R.</Author>
-<Author>Tang, Y.</Author>
-<Author>Ball, H.</Author>
-<Author>Sangras, B.</Author>
-<Author>Kim, S.C.</Author>
-<Author>Falck, J.R.</Author>
-<Author>Peng, J.</Author>
-<Author>Gu, W.</Author>
-<Author>Zhao, Y.</Author>
-</Authors>
-<Citation>Mol. Cell. Proteomics 6, 812-819, 2007</Citation>
-<Title>Lysine propionylation and butyrylation are novel post-translational modifications in histones.</Title>
-<Xref>DOI:10.1074/mcp.M700021-MCP200</Xref>
-<Xref>PMID:17267393</Xref>
-<Note>the modification is not chemically characterized and isobaric alternatives are not eliminated</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Garrity, J.</Author>
-<Author>Gardner, J.G.</Author>
-<Author>Hawse, W.</Author>
-<Author>Wolberger, C.</Author>
-<Author>Escalante-Semerena, J.C.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 282, 30239-30245, 2007</Citation>
-<Title>N-lysine propionylation controls the activity of propionyl-CoA synthetase.</Title>
-<Xref>DOI:10.1074/jbc.M704409200</Xref>
-<Xref>PMID:17684016</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Vollmuth, F.</Author>
-<Author>Geyer, M.</Author>
-</Authors>
-<Citation>Angew. Chem. Int. Ed. Engl. 49, 6768-6772, 2010</Citation>
-<Title>Interaction of propionylated and butyrylated histone H3 lysine marks with Brd4 bromodomains.</Title>
-<Xref>DOI:10.1002/anie.201002724</Xref>
-<Xref>PMID:20715035</Xref>
-<Note>X-ray diffraction, 1.75 angstroms; iosthermal titration calorimetry; binding of propanoylated lysine histone peptide is found to be unspecific and weaker than for the corresponding acetylated peptide</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Vollmuth, V.</Author>
-<Author>Geyer, M.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, May 2010</Citation>
-<Description>Crystal structure of Brd4 bromodomain 1 with propionylated histone H3-K(buty)14.</Description>
-<Xref>PDB:3MUK</Xref>
-<Note>X-ray diffraction, 1.75 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bheda, P.</Author>
-<Author>Wang, J.T.</Author>
-<Author>Escalante-Semerena, J.C.</Author>
-<Author>Wolberger, C.</Author>
-</Authors>
-<Citation>Protein Sci. 20, 131-139, 2011</Citation>
-<Title>Structure of Sir2Tm bound to a propionylated peptide.</Title>
-<Xref>DOI:10.1002/pro.544</Xref>
-<Xref>PMID:21080423</Xref>
-<Note>X-ray diffraction, 1.8 angstroms; artificial peptide complexed with protein that naturally binds N6-acetyllysine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wolberger, C.</Author>
-<Author>Bheda, P.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, October 2010</Citation>
-<Description>Structure of Sir2Tm bound to a propionylated peptide.</Description>
-<Xref>PDB:3PDH</Xref>
-<Note>X-ray diffraction, 1.80 angstroms</Note>
-</ReferenceBlock>
-<Comment>A metabolic source for propanoic acid in the nucleus is not evident; the modification would be isobaric with lactaldehyde adduct, an advanced glycation end product of artifactual nucleic acid degradation</Comment>
-<Comment>This modification has been shown to be produced by Gcn-5-related N-acetyltransferases in some bacterial systems.</Comment>
-<Comment>In eukaryotes, a metabolic source for propanoic acid in the nucleus is not evident, and a responsible generating enzyme activity is not identified.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>lysine N6-acyltransferase, acetoin utilization protein AcuA (EC 2.3.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>PSI-MOD:01398</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lipoprotein</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0475.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0475.PDB" />
-</Entry>
-<Entry id="AA0476">
-<Header>
-<Code>AA0476</Code>
-<Dates>
-<CreationDate>05-Dec-2008</CreationDate>
-<StrucRevDate>05-Dec-2008</StrucRevDate>
-<TextChngDate>30-Jun-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6-(ADP-ribosyl)-L-lysine</Name>
-<AlternateName>2-amino-6-(ADP-ribosyl)amino-hexanoic acid</AlternateName>
-<AlternateName>epsilon-ADP-ribosyllysine</AlternateName>
-<AlternateName>N(zeta)-ADP-ribosyllysine</AlternateName>
-<AlternateName>N6-alpha-D-ribofuranosyl-L-lysine 5'-&gt;5'-ester with adenosine 5'-(trihydrogen diphosphate)</AlternateName>
-<AlternateName>N6-[alpha-D-ribofuranoside 5'-&gt;5'-ester with adenosine 5'-(trihydrogen diphosphate)]-L-lysine</AlternateName>
-<SystematicName>(S)-2-amino-6-([adenosine 5'-(trihydrogen diphosphate) 5'-&gt;5'-ester with alpha-D-ribofuranosyl]amino)hexanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 21 H 33 N 7 O 14 P 2</Formula>
-<Weight type="chemical">669.48</Weight>
-<Weight type="physical">669.156072</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 15 H 21 N 5 O 13 P 2</Formula>
-<Weight type="chemical">541.30</Weight>
-<Weight type="physical">541.061109</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Haenni, S.S.</Author>
-<Author>Hassa, P.O.</Author>
-<Author>Altmeyer, M.</Author>
-<Author>Fey, M.</Author>
-<Author>Imhof, R.</Author>
-<Author>Hottiger, M.O.</Author>
-</Authors>
-<Citation>Int. J. Biochem. Cell Biol. 40, 2274-2283, 2008</Citation>
-<Title>Identification of lysines 36 and 37 of PARP-2 as targets for acetylation and auto-ADP-ribosylation.</Title>
-<Xref>DOI:10.1016/j.biocel.2008.03.008</Xref>
-<Xref>PMID:18436469</Xref>
-</ReferenceBlock>
-<Comment>The alpha form is presented.</Comment>
-<Comment>The keyword "phosphoprotein" is not used with ADP-ribosylation.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>NAD(P)+--lysine ADP-ribosyltransferase (EC 2.4.2.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>PSI-MOD:01399</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>*phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n6-(adp-ribosyl)lysine__k">MOD_RES N6-(ADP-ribosyl)lysine</Feature>
-</Features>
-<Image src="/images/AA0476.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0476.PDB" />
-</Entry>
-<Entry id="AA0477">
-<Header>
-<Code>AA0477</Code>
-<Dates>
-<CreationDate>05-Dec-2008</CreationDate>
-<StrucRevDate>05-Dec-2008</StrucRevDate>
-<TextChngDate>30-Jan-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-lysyl-poly(ADP-ribose)</Name>
-<SystematicName>poly[2'-adenosine 5'-(trihydrogen diphosphate) 5'-&gt;5'-ester with 1alpha-D-ribofuranosyl] (2S)-2,6-diaminohexanoate</SystematicName>
-<Xref>CAS:26656-46-2</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 21 H 34 N 7 O 15 P 2 +</Formula>
-<Weight type="chemical">686.48 +</Weight>
-<Weight type="physical">686.158812 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 15 H 21 N 5 O 13 P 2 +</Formula>
-<Weight type="chemical">541.30 +</Weight>
-<Weight type="physical">541.061109 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ogata, N.</Author>
-<Author>Ueda, K.</Author>
-<Author>Kagamiyama, H.</Author>
-<Author>Hayaishi, O.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 255, 7616-7620, 1980</Citation>
-<Title>ADP-ribosylation of histone H1. Identification of glutamic acid residues 2, 14, and the COOH-terminal lysine residue as modification sites.</Title>
-<Xref>PMID:6772638</Xref>
-</ReferenceBlock>
-<Comment>The alpha form is presented.</Comment>
-<Comment>The keyword "phosphoprotein" is not used with ADP-ribosylation.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>NAD+ ADP-ribosyltransferase (EC 2.4.2.30)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>PSI-MOD:01400</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>*phosphoprotein</Keyword>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>poly adenosine diphosphate ribose</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__lysyl polyadp-ribose__k">MOD_RES Lysyl poly(ADP-ribose)</Feature>
-</Features>
-<Image src="/images/AA0477.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0477.PDB" />
-</Entry>
-<Entry id="AA0478">
-<Header>
-<Code>AA0478</Code>
-<Dates>
-<CreationDate>31-Dec-2008</CreationDate>
-<StrucRevDate>31-Dec-2008</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>(2S,3S)-3-hydroxyasparagine</Name>
-<AlternateName>(2S,3S)-2,4-diamino-3-hydroxy-4-oxobutanoic acid</AlternateName>
-<AlternateName>(3S)-3-hydroxy-L-asparagine</AlternateName>
-<AlternateName>L-threo-beta-hydroxyasparagine</AlternateName>
-<SystematicName>(2S,3S)-2-amino-3-hydroxy-4-butanediamic acid</SystematicName>
-<Xref>ChEBI:138107</Xref>
-<Xref>PDBHET:AHB</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 6 N 2 O 3</Formula>
-<Weight type="chemical">130.10</Weight>
-<Weight type="physical">130.037842</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0003">
-<Formula>C 0 H 0 N 0 O 1</Formula>
-<Weight type="chemical">16.00</Weight>
-<Weight type="physical">15.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lando, D.</Author>
-<Author>Peet, D.J.</Author>
-<Author>Whelan, D.A.</Author>
-<Author>Gorman, J.J.</Author>
-<Author>Whitelaw, M.L.</Author>
-</Authors>
-<Citation>Science 295, 858-861, 2002</Citation>
-<Title>Asparagine hydroxylation of the HIF transactivation domain a hypoxic switch.</Title>
-<Xref>DOI:10.1126/science.1068592</Xref>
-<Xref>PMID:11823643</Xref>
-<Note>mass spectrometric detection; located in the C-terminal transactivation domain; the stereochemistry was not determined</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hewitson, K.S.</Author>
-<Author>McNeill, L.A.</Author>
-<Author>Riordan, M.V.</Author>
-<Author>Tian, Y.M.</Author>
-<Author>Bullock, A.N.</Author>
-<Author>Welford, R.W.</Author>
-<Author>Elkins, J.M.</Author>
-<Author>Oldham, N.J.</Author>
-<Author>Bhattacharya, S.</Author>
-<Author>Gleadle, J.M.</Author>
-<Author>Ratcliffe, P.J.</Author>
-<Author>Pugh, C.W.</Author>
-<Author>Schofield, C.J.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 277, 26351-26355, 2002</Citation>
-<Title>Hypoxia-inducible factor (HIF) asparagine hydroxylase is identical to factor inhibiting HIF (FIH) and is related to the cupin structural family.</Title>
-<Xref>DOI:10.1074/jbc.C200273200</Xref>
-<Xref>PMID:12042299</Xref>
-<Note>characterization of the enzyme producing the modification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>McNeill, L.A.</Author>
-<Author>Hewitson, K.S.</Author>
-<Author>Claridge, T.D.</Author>
-<Author>Seibel, J.F.</Author>
-<Author>Horsfall, L.E.</Author>
-<Author>Schofield, C.J.</Author>
-</Authors>
-<Citation>Biochem. J. 367, 571-575, 2002</Citation>
-<Title>Hypoxia-inducible factor asparaginyl hydroxylase (FIH-1) catalyses hydroxylation at the beta-carbon of asparagine-803.</Title>
-<Xref>DOI:10.1042/BJ20021162</Xref>
-<Xref>PMID:12215170</Xref>
-<Note>the modification is identified as the (2S,3S), threo, diastereomer </Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Coleman, M.L.</Author>
-<Author>McDonough, M.A.</Author>
-<Author>Hewitson, K.S.</Author>
-<Author>Coles, C.</Author>
-<Author>Mecinovic, J.</Author>
-<Author>Edelmann, M.</Author>
-<Author>Cook, K.M.</Author>
-<Author>Cockman, M.E.</Author>
-<Author>Lancaster, D.E.</Author>
-<Author>Kessler, B.M.</Author>
-<Author>Oldham, N.J.</Author>
-<Author>Ratcliffe, P.J.</Author>
-<Author>Schofield, C.J.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 282, 24027-24038, 2007</Citation>
-<Title>Asparaginyl hydroxylation of the Notch ankyrin repeat domain by factor inhibiting hypoxia-inducible factor.</Title>
-<Xref>DOI:10.1074/jbc.M704102200</Xref>
-<Xref>PMID:17573339</Xref>
-<Note>mass spectrometric detection; X-ray diffraction, 2.35 angstroms; located in the ankyrin repeat domains of notch 1</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>McDonough, M.A.</Author>
-<Author>Schofield, C.J.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, June 2007</Citation>
-<Description>Mouse notch 1 ankyrin repeat intracellular domain.</Description>
-<Xref>PDB:2QC9</Xref>
-<Note>X-ray diffraction, 2.35 angstroms</Note>
-</ReferenceBlock>
-<Comment>This diastereomeric form has been found in the C-terminal transactivation domain (CAD) of hypoxia-inducible factor (HIF), and in the ankyrin repeat domains of notch 1, which probably also contains the other diastereomeric form of the modification in its EGF domains.</Comment>
-<Comment>The PDB group code includes models with both the (2S,3R) and the (2S,3S) stereoconfiguration.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>hypoxia-inducible factor-asparagine dioxygenase (EC 1.14.11.30)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>N</SequenceSpec>
-<Xref>PSI-MOD:01401</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__(3S)-3-hydroxyasparagine__n">MOD_RES (3S)-3-hydroxyasparagine</Feature>
-</Features>
-<Image src="/images/AA0478.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0478.PDB" />
-</Entry>
-<Entry id="AA0479">
-<Header>
-<Code>AA0479</Code>
-<Dates>
-<CreationDate>31-Dec-2008</CreationDate>
-<StrucRevDate>31-Dec-2008</StrucRevDate>
-<TextChngDate>31-Mar-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>(2S,3R,4R)-3,4-dihydroxyproline</Name>
-<AlternateName>2,3-trans-3,4-trans-3,4-dihydroxy-L-proline</AlternateName>
-<AlternateName>2-alpha-3-beta-4-alpha-3,4-dihydroxyproline</AlternateName>
-<SystematicName>(2S,3R,4R)-3,4-dihydroxypyrrolidine-2-carboxylic acid</SystematicName>
-<Xref>CAS:74644-88-5</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 7 N 1 O 3</Formula>
-<Weight type="chemical">129.12</Weight>
-<Weight type="physical">129.042593</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0015">
-<Formula>C 0 H 0 N 0 O 2</Formula>
-<Weight type="chemical">32.00</Weight>
-<Weight type="physical">31.989829</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Faulstich, H.</Author>
-<Author>Buku, A.</Author>
-<Author>Bodenmüller, H.</Author>
-<Author>Wieland, T.</Author>
-</Authors>
-<Citation>Biochemistry 19, 3334-3343, 1980</Citation>
-<Title>Virotoxins: actin-binding cyclic peptides of Amanita virosa mushrooms.</Title>
-<Xref>DOI:10.1021/bi00555a036</Xref>
-<Xref>PMID:6893271</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Buku, A.</Author>
-<Author>Faulstich, H.</Author>
-<Author>Wieland, T.</Author>
-<Author>Dabrowski, J.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 77, 2370-2371, 1980</Citation>
-<Title>2,3-trans-3,4-trans-3,4-Dihydroxy-L-proline: An amino acid in toxic peptides of Amanita virosa mushrooms.</Title>
-<Xref>DOI:10.1073/pnas.77.5.2370</Xref>
-<Xref>PMID:16592813</Xref>
-<Note>chemical characteriztion, stereochemistry, (1)H-NMR identification</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>P</SequenceSpec>
-<Xref>PSI-MOD:01402</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__(3r,4r)-3,4-dihydroxyproline__p">MOD_RES (3R,4R)-3,4-dihydroxyproline</Feature>
-</Features>
-<Image src="/images/AA0479.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0479.PDB" />
-</Entry>
-<Entry id="AA0480">
-<Header>
-<Code>AA0480</Code>
-<Dates>
-<CreationDate>31-Dec-2008</CreationDate>
-<StrucRevDate>31-Dec-2008</StrucRevDate>
-<TextChngDate>30-Jan-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>(2S)-4,5,5'-trihydroxyleucine</Name>
-<AlternateName>4,5,5'-trihydroxyleucine</AlternateName>
-<AlternateName>gamma,delta,delta'-trihydroxyleucine</AlternateName>
-<SystematicName>(2S)-2-amino-4,5-dihydroxy-4-(hydroxymethyl)pentanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 11 N 1 O 4</Formula>
-<Weight type="chemical">161.16</Weight>
-<Weight type="physical">161.068808</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0011">
-<Formula>C 0 H 0 N 0 O 3</Formula>
-<Weight type="chemical">48.00</Weight>
-<Weight type="physical">47.984744</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Faulstich, H.</Author>
-<Author>Buku, A.</Author>
-<Author>Bodenmüller, H.</Author>
-<Author>Wieland, T.</Author>
-</Authors>
-<Citation>Biochemistry 19, 3334-3343, 1980</Citation>
-<Title>Virotoxins: actin-binding cyclic peptides of Amanita virosa mushrooms.</Title>
-<Xref>DOI:10.1021/bi00555a036</Xref>
-<Xref>PMID:6893271</Xref>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>L</SequenceSpec>
-<Xref>PSI-MOD:01403</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__4,5,5'-trihydroxyleucine__l">MOD_RES 4,5,4'-trihydroxyleucine</Feature>
-</Features>
-<Image src="/images/AA0480.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0480.PDB" />
-</Entry>
-<Entry id="AA0481">
-<Header>
-<Code>AA0481</Code>
-<Dates>
-<CreationDate>30-Jan-2009</CreationDate>
-<StrucRevDate>30-Jan-2009</StrucRevDate>
-<TextChngDate>25-Feb-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-asparagine thiazole-4-carboxylic acid</Name>
-<AlternateName>2-[1,3-bisazanyl-3-oxopropyl]-1,3-thiazole-4-carboxylic acid</AlternateName>
-<SystematicName>2-[(1S)-1,3-diamino-3-oxopropyl]-1,3-thiazole-4-carboxylic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 7 N 3 O 2 S 1</Formula>
-<Weight type="chemical">197.21</Weight>
-<Weight type="physical">197.025897</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0003 AA0005">
-<Formula>C 0 H -4 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-20.03</Weight>
-<Weight type="physical">-20.026215</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Stella, S.</Author>
-<Author>Montanini, N.</Author>
-<Author>Le Monnier, F.</Author>
-<Author>Ferrari, P.</Author>
-<Author>Colombo, L.</Author>
-<Author>Marinelli, F.</Author>
-<Author>Landini, P.</Author>
-<Author>Ciciliato, I.</Author>
-<Author>Goldstein, B.P.</Author>
-<Author>Selva, E.</Author>
-</Authors>
-<Citation>J. Antibiot. 48, 780-786, 1995</Citation>
-<Title>Antibiotic GE37468 A: a new inhibitor of bacterial protein synthesis. I. Isolation and characterization.</Title>
-<Xref>PMID:7592021</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ferrari, P.</Author>
-<Author>Colombo, L.</Author>
-<Author>Stella, S.</Author>
-<Author>Selva, E.</Author>
-<Author>Zerilli, L.F.</Author>
-</Authors>
-<Citation>J. Antibiot. 48, 1304-1311, 1995</Citation>
-<Title>Antibiotic GE37468 A: a novel inhibitor of bacterial protein synthesis. II. Structure elucidation.</Title>
-<Xref>PMID:8557573</Xref>
-<Note>mass spectrometric, (1)H-NMR and (13)C-NMR analysis; chemical characterization</Note>
-</ReferenceBlock>
-<Comment>Formed by the condensation of a cysteine thiol with the carbonyl of the preceding residue and alpha-beta dehydrogenation.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptidyl-cysteine cyclase (EC 4.2.1.-)</EnzymeName>
-<EnzymeName>peptidyl-thiazoline dehydrogenase (EC 1.3.-.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C, N</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Xref>PSI-MOD:01404</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>oxazole/thiazole ring</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__thiazole-4-carboxylic acid (asn-cys)__n__c">CROSSLNK Thiazole-4-carboxylic acid (Asn-Cys)</Feature>
-</Features>
-<Image src="/images/AA0481.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0481.PDB" />
-</Entry>
-<Entry id="AA0482">
-<Header>
-<Code>AA0482</Code>
-<Dates>
-<CreationDate>30-Jan-2009</CreationDate>
-<StrucRevDate>30-Jan-2009</StrucRevDate>
-<TextChngDate>29-Nov-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-proline thiazole-4-carboxylic acid</Name>
-<SystematicName>2-[(2S)-pyrrolidin-2-yl]-1,3-thiazole-4-carboxylic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 8 H 8 N 2 O 1 S 1</Formula>
-<Weight type="chemical">180.22</Weight>
-<Weight type="physical">180.035734</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0015">
-<Formula>C 0 H -4 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-20.03</Weight>
-<Weight type="physical">-20.026215</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Stella, S.</Author>
-<Author>Montanini, N.</Author>
-<Author>Le Monnier, F.</Author>
-<Author>Ferrari, P.</Author>
-<Author>Colombo, L.</Author>
-<Author>Marinelli, F.</Author>
-<Author>Landini, P.</Author>
-<Author>Ciciliato, I.</Author>
-<Author>Goldstein, B.P.</Author>
-<Author>Selva, E.</Author>
-</Authors>
-<Citation>J. Antibiot. 48, 780-786, 1995</Citation>
-<Title>Antibiotic GE37468 A: a new inhibitor of bacterial protein synthesis. I. Isolation and characterization.</Title>
-<Xref>PMID:7592021</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ferrari, P.</Author>
-<Author>Colombo, L.</Author>
-<Author>Stella, S.</Author>
-<Author>Selva, E.</Author>
-<Author>Zerilli, L.F.</Author>
-</Authors>
-<Citation>J. Antibiot. 48, 1304-1311, 1995</Citation>
-<Title>Antibiotic GE37468 A: a novel inhibitor of bacterial protein synthesis. II. Structure elucidation.</Title>
-<Xref>PMID:8557573</Xref>
-<Note>mass spectrometric, (1)H-NMR and (13)C-NMR analysis; chemical characterization</Note>
-</ReferenceBlock>
-<Comment>Formed by the condensation of a cysteine thiol with the carbonyl of the preceding residue and alpha-beta dehydrogenation.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptidyl-cysteine cyclase (EC 4.2.1.-)</EnzymeName>
-<EnzymeName>peptidyl-thiazoline dehydrogenase (EC 1.3.-.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C, P</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Xref>PSI-MOD:01405</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>oxazole/thiazole ring</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__thiazole-4-carboxylic acid (pro-cys)__p__c">CROSSLNK Thiazole-4-carboxylic acid (Pro-Cys)</Feature>
-</Features>
-<Image src="/images/AA0482.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0482.PDB" />
-</Entry>
-<Entry id="AA0483">
-<Header>
-<Code>AA0483</Code>
-<Dates>
-<CreationDate>30-Jan-2009</CreationDate>
-<StrucRevDate>30-Jan-2009</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-threonine thiazole-4-carboxylic acid</Name>
-<AlternateName>2-[1-azanyl-2-hydroxypropyl]-1,3-thiazole-4-carboxylic acid</AlternateName>
-<SystematicName>2-[(1S,2R)-1-amino-2-hydroxypropyl]-1,3-thiazole-4-carboxylic acid</SystematicName>
-<Xref>PDBHET:XAA</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 8 N 2 O 2 S 1</Formula>
-<Weight type="chemical">184.21</Weight>
-<Weight type="physical">184.030649</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0017">
-<Formula>C 0 H -4 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-20.03</Weight>
-<Weight type="physical">-20.026215</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bond, C.S.</Author>
-<Author>Shaw, M.P.</Author>
-<Author>Alphey, M.S.</Author>
-<Author>Hunter, W.N.</Author>
-</Authors>
-<Citation>Acta Crystallogr. D Biol. Crystallogr. 57, 755-758, 2001</Citation>
-<Title>Structure of the macrocycle thiostrepton solved using the anomalous dispersion contribution of sulfur.</Title>
-<Xref>DOI:10.1107/S0907444901003134</Xref>
-<Xref>PMID:11320328</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bond, C.S.</Author>
-<Author>Shaw, M.P.</Author>
-<Author>Alphey, M.S.</Author>
-<Author>Hunter, W.N.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, October 2000</Citation>
-<Description>Structure of the macrocycle thiostrepton solved using the anomalous dispersion contribution of sulfur.</Description>
-<Xref>PDB:1E9W</Xref>
-<Note>X-ray diffraction, 1.02 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kalyon, B.</Author>
-<Author>Helaly, S.E.</Author>
-<Author>Scholz, R.</Author>
-<Author>Nachtigall, J.</Author>
-<Author>Vater, J.</Author>
-<Author>Borriss, R.</Author>
-<Author>Süssmuth, R.D.</Author>
-</Authors>
-<Citation>Org. Lett. 13, 2996-2999, 2011</Citation>
-<Title>Plantazolicin A and B: Structure Elucidation of Ribosomally Synthesized Thiazole/Oxazole Peptides from Bacillus amyloliquefaciens FZB42.</Title>
-<Xref>DOI:10.1021/ol200809m</Xref>
-<Xref>PMID:21568297</Xref>
-<Note>mass spectrometric, (1)H-NMR, (13)C-NMR and (15)N-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Molohon, K.J.</Author>
-<Author>Melby, J.O.</Author>
-<Author>Lee, J.</Author>
-<Author>Evans, B.S.</Author>
-<Author>Dunbar, K.L.</Author>
-<Author>Bumpus, S.B.</Author>
-<Author>Kelleher, N.L.</Author>
-<Author>Mitchell, D.A.</Author>
-</Authors>
-<Citation>ACS Chem. Biol. 6, 1307-1313, 2011</Citation>
-<Title>Structure determination and interception of biosynthetic intermediates for the plantazolicin class of highly discriminating antibiotics.</Title>
-<Xref>DOI:10.1021/cb200339d</Xref>
-<Xref>PMID:21950656</Xref>
-<Note>mass spectrometric, (1)H-NMR and (13)C-NMR identification</Note>
-</ReferenceBlock>
-<Comment>Formed by the condensation of a cysteine thiol with the carbonyl of the preceding residue and alpha-beta dehydrogenation.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptidyl-cysteine cyclase (EC 4.2.1.-)</EnzymeName>
-<EnzymeName>peptidyl-thiazoline dehydrogenase (EC 1.3.-.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C, T</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Xref>PSI-MOD:01406</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>oxazole/thiazole ring</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__thiazole-4-carboxylic acid (thr-cys)__t__c">CROSSLNK Thiazole-4-carboxylic acid (Thr-Cys)</Feature>
-</Features>
-<Image src="/images/AA0483.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0483.PDB" />
-</Entry>
-<Entry id="AA0484">
-<Header>
-<Code>AA0484</Code>
-<Dates>
-<CreationDate>30-Jan-2009</CreationDate>
-<StrucRevDate>30-Jan-2009</StrucRevDate>
-<TextChngDate>25-Feb-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-phenylalanine thiazoline-4-carboxylic acid</Name>
-<AlternateName>2-[1-azanyl-2-phenylethyl]-4,5-dihydro-1,3-thiazole-4-carboxylic acid</AlternateName>
-<SystematicName>(4R)-2-[(1S)-1-amino-2-phenylethyl]-4,5-dihydro-1,3-thiazole-4-carboxylic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 12 H 12 N 2 O 1 S 1</Formula>
-<Weight type="chemical">232.30</Weight>
-<Weight type="physical">232.067034</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0014 AA0005">
-<Formula>C 0 H -2 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Stella, S.</Author>
-<Author>Montanini, N.</Author>
-<Author>Le Monnier, F.</Author>
-<Author>Ferrari, P.</Author>
-<Author>Colombo, L.</Author>
-<Author>Marinelli, F.</Author>
-<Author>Landini, P.</Author>
-<Author>Ciciliato, I.</Author>
-<Author>Goldstein, B.P.</Author>
-<Author>Selva, E.</Author>
-</Authors>
-<Citation>J. Antibiot. 48, 780-786, 1995</Citation>
-<Title>Antibiotic GE37468 A: a new inhibitor of bacterial protein synthesis. I. Isolation and characterization.</Title>
-<Xref>PMID:7592021</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ferrari, P.</Author>
-<Author>Colombo, L.</Author>
-<Author>Stella, S.</Author>
-<Author>Selva, E.</Author>
-<Author>Zerilli, L.F.</Author>
-</Authors>
-<Citation>J. Antibiot. 48, 1304-1311, 1995</Citation>
-<Title>Antibiotic GE37468 A: a novel inhibitor of bacterial protein synthesis. II. Structure elucidation.</Title>
-<Xref>PMID:8557573</Xref>
-<Note>mass spectrometric, (1)H-NMR and (13)C-NMR analysis; chemical characterization</Note>
-</ReferenceBlock>
-<Comment>Formed by the condensation of a cysteine thiol with the carbonyl of the preceding residue.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptidyl-cysteine cyclase (EC 4.2.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C, F</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Xref>PSI-MOD:01407</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>oxazole/thiazole ring</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__thiazoline-4-carboxylic acid (phe-cys)__f__c">CROSSLNK Thiazoline-4-carboxylic acid (Phe-Cys)</Feature>
-</Features>
-<Image src="/images/AA0484.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0484.PDB" />
-</Entry>
-<Entry id="AA0485">
-<Header>
-<Code>AA0485</Code>
-<Dates>
-<CreationDate>30-Jan-2009</CreationDate>
-<StrucRevDate>12-Jun-2009</StrucRevDate>
-<TextChngDate>31-Dec-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-threonine (4S)-thiazoline-4-carboxylic acid</Name>
-<AlternateName>2-[1-azanyl-2-hydroxypropyl]-4,5-dihydro-1,3-thiazole-4-carboxylic acid</AlternateName>
-<SystematicName>(4S)-2-[(1S,2R)-1-amino-2-hydroxypropyl]-4,5-dihydro-1,3-thiazole-4-carboxylic acid</SystematicName>
-<Xref>PDBHET:BB9</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 10 N 2 O 2 S 1</Formula>
-<Weight type="chemical">186.23</Weight>
-<Weight type="physical">186.046299</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0017">
-<Formula>C 0 H -2 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bond, C.S.</Author>
-<Author>Shaw, M.P.</Author>
-<Author>Alphey, M.S.</Author>
-<Author>Hunter, W.N.</Author>
-</Authors>
-<Citation>Acta Crystallogr. D Biol. Crystallogr. 57, 755-758, 2001</Citation>
-<Title>Structure of the macrocycle thiostrepton solved using the anomalous dispersion contribution of sulfur.</Title>
-<Xref>DOI:10.1107/S0907444901003134</Xref>
-<Xref>PMID:11320328</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bond, C.S.</Author>
-<Author>Shaw, M.P.</Author>
-<Author>Alphey, M.S.</Author>
-<Author>Hunter, W.N.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, October 2000</Citation>
-<Description>Structure of the macrocycle thiostrepton solved using the anomalous dispersion contribution of sulfur.</Description>
-<Xref>PDB:1E9W</Xref>
-<Note>X-ray diffraction, 1.02 angstroms</Note>
-</ReferenceBlock>
-<Comment>Formed by the condensation of a cysteine thiol with the carbonyl of the preceding residue. The ring may be oxidized to thiazole and then reduced from the opposite side effectively inverting the cysteine alpha-carbon chirality.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptidyl-cysteine cyclase (EC 4.2.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C, T</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Xref>PSI-MOD:01408</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>oxazole/thiazole ring</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__(4s)-thiazoline-4-carboxylic acid (thr-cys)__t__c">CROSSLNK (4S)-thiazoline-4-carboxylic acid (Thr-Cys)</Feature>
-</Features>
-<Image src="/images/AA0485.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0485.PDB" />
-</Entry>
-<Entry id="AA0486">
-<Header>
-<Code>AA0486</Code>
-<Dates>
-<CreationDate>31-Mar-2009</CreationDate>
-<StrucRevDate>31-Mar-2009</StrucRevDate>
-<TextChngDate>31-Mar-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>1-amino-2-propanone</Name>
-<AlternateName>1-aminopropan-2-one</AlternateName>
-<AlternateName>aminoacetone</AlternateName>
-<SystematicName>1-aminopropanone</SystematicName>
-<Xref>CAS:298-08-8</Xref>
-<Xref>ChEBI:17906</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 6 N 1 O 1</Formula>
-<Weight type="chemical">72.09</Weight>
-<Weight type="physical">72.044939</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0017">
-<Formula>C -1 H -2 N 0 O -2</Formula>
-<Weight type="chemical">-46.03</Weight>
-<Weight type="physical">-46.005479</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Suzumura, K.</Author>
-<Author>Yokoi, T.</Author>
-<Author>Funatsu, M.</Author>
-<Author>Nagai, K.</Author>
-<Author>Tanaka, K.</Author>
-<Author>Zhang, H.</Author>
-<Author>Suzuki, K.</Author>
-</Authors>
-<Citation>J. Antibiot. 56, 129-134, 2003</Citation>
-<Title>YM-266183 and YM-266184, novel thiopeptide antibiotics produced by Bacillus cereus isolated from a marine sponge II. Structure elucidation.</Title>
-<Xref>PMID:12715872</Xref>
-<Note>mass spectrometric, (1)H-NMR, and (13)C-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wieland Brown, L.C.</Author>
-<Author>Acker, M.G.</Author>
-<Author>Clardy, J.</Author>
-<Author>Walsh, C.T.</Author>
-<Author>Fischbach, M.A.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 106, 2549-2553, 2009</Citation>
-<Title>Thirteen posttranslational modifications convert a 14-residue peptide into the antibiotic thiocillin.</Title>
-<Xref>DOI:10.1073/pnas.0900008106</Xref>
-<Xref>PMID:19196969</Xref>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>T</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>PSI-MOD:01433</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__1-amino-2-propanone__t">MOD_RES 1-amino-2-propanone</Feature>
-</Features>
-<Image src="/images/AA0486.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0486.PDB" />
-</Entry>
-<Entry id="AA0487">
-<Header>
-<Code>AA0487</Code>
-<Dates>
-<CreationDate>31-Mar-2009</CreationDate>
-<StrucRevDate>31-Mar-2009</StrucRevDate>
-<TextChngDate>30-Sep-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>4-hydroxy-L-glutamic acid</Name>
-<AlternateName>gamma-hydroxy glutaminic acid</AlternateName>
-<AlternateName>threo-4-hydroxy-L-glutamic acid</AlternateName>
-<SystematicName>(2S,4Xi)-2-amino-4-hydroxypentanedioic acid</SystematicName>
-<Xref>CAS:3913-68-6</Xref>
-<Xref>PDBHET:3GL</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 7 N 1 O 4</Formula>
-<Weight type="chemical">145.11</Weight>
-<Weight type="physical">145.037508</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0006">
-<Formula>C 0 H 0 N 0 O 1</Formula>
-<Weight type="chemical">16.00</Weight>
-<Weight type="physical">15.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Pascard, C.</Author>
-<Author>Ducruix, A.</Author>
-<Author>Lunel, J.</Author>
-<Author>Prangé, T.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 99, 6418-6423, 1977</Citation>
-<Title>Highly modified cysteine-containing antibiotics. Chemical structure and configuration of nosiheptide.</Title>
-<Xref>DOI:10.1021/ja00461a039</Xref>
-<Xref>PMID:893891</Xref>
-<Note>X-ray diffraction; the resolution is not specified; the structure deposited in the Cambridge Structural Database (NOSHEP10) is presented as (2S,4R)</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Harms, J.M.</Author>
-<Author>Wilson, D.N.</Author>
-<Author>Schluenzen, F.</Author>
-<Author>Connell, S.R.</Author>
-<Author>Stachelhaus, T.</Author>
-<Author>Zaborowska, Z.</Author>
-<Author>Spahn, C.M.</Author>
-<Author>Fucini, P.</Author>
-</Authors>
-<Citation>Mol. Cell 30, 26-38, 2008</Citation>
-<Title>Translational regulation via L11: molecular switches on the ribosome turned on and off by thiostrepton and micrococcin.</Title>
-<Xref>DOI:10.1016/j.molcel.2008.01.009</Xref>
-<Xref>PMID:18406324</Xref>
-<Note>X-ray diffraction, 2.50 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Harms, J.M.</Author>
-<Author>Wilson, D.N.</Author>
-<Author>Schluenzen, F.</Author>
-<Author>Connell, S.R.</Author>
-<Author>Stachelhaus, T.</Author>
-<Author>Zaborowska, Z.</Author>
-<Author>Spahn, C.M.</Author>
-<Author>Fucini, P.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, March 2008</Citation>
-<Description>Thiopeptide antibiotic nosiheptide bound to the large ribosomal subunit of Deinococcus radiodurans.</Description>
-<Xref>PDB:2ZJP</Xref>
-<Note>X-ray diffraction, 3.70 angstroms; the structure is presented as (2S,4S)</Note>
-</ReferenceBlock>
-<Comment>This modification is currently represented in the PDB as part of the HET group for the entire molecule of nosiheptide.</Comment>
-<Comment>The chirality of C-4 is not settled. The (2S,4S) diastereomer is shown.</Comment>
-<SequenceCode>
-<SequenceSpec>E</SequenceSpec>
-<Condition>incidental to RESID:AA0488</Condition>
-<Condition>incidental to RESID:AA0541</Condition>
-<Xref>PSI-MOD:01434</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="mod_res__4-hydroxyglutamate__e">MOD_RES 4-hydroxyglutamate</Feature>
-</Features>
-<Image src="/images/AA0487.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0487.PDB" />
-</Entry>
-<Entry id="AA0488">
-<Header>
-<Code>AA0488</Code>
-<Dates>
-<CreationDate>31-Mar-2009</CreationDate>
-<StrucRevDate>31-Mar-2009</StrucRevDate>
-<TextChngDate>30-Sep-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>2-(cystein-S-ylcarbonyl)-3-methyl-4-(glutam-5-yloxy)methylindole</Name>
-<AlternateName>2-(cystein-S-ylcarbonyl)-4-[(glutam-5-yloxy)methyl]-3-methyl-1H-indole</AlternateName>
-<SystematicName>2-([(1R)-1-amino-1-carboxyeth-2-yl]sulfanyl)carbonyl-3-methyl-4-([(1S)-1-amino-1-carboxy-4-oxobutan-4-yl]oxy)methyl-1H-indole</SystematicName>
-<Xref>PDBHET:NO1</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 19 H 19 N 3 O 5 S 1</Formula>
-<Weight type="chemical">401.44</Weight>
-<Weight type="physical">401.104542</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0006">
-<Formula>C 11 H 7 N 1 O 1 S 0</Formula>
-<Weight type="chemical">169.18</Weight>
-<Weight type="physical">169.052764</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Pascard, C.</Author>
-<Author>Ducruix, A.</Author>
-<Author>Lunel, J.</Author>
-<Author>Prangé, T.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 99, 6418-6423, 1977</Citation>
-<Title>Highly modified cysteine-containing antibiotics. Chemical structure and configuration of nosiheptide.</Title>
-<Xref>DOI:10.1021/ja00461a039</Xref>
-<Xref>PMID:893891</Xref>
-<Note>X-ray diffraction; the resolution is not specified; the structure is deposited in the Cambridge Structural Database entry NOSHEP10</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Harms, J.M.</Author>
-<Author>Wilson, D.N.</Author>
-<Author>Schluenzen, F.</Author>
-<Author>Connell, S.R.</Author>
-<Author>Stachelhaus, T.</Author>
-<Author>Zaborowska, Z.</Author>
-<Author>Spahn, C.M.</Author>
-<Author>Fucini, P.</Author>
-</Authors>
-<Citation>Mol. Cell 30, 26-38, 2008</Citation>
-<Title>Translational regulation via L11: molecular switches on the ribosome turned on and off by thiostrepton and micrococcin.</Title>
-<Xref>DOI:10.1016/j.molcel.2008.01.009</Xref>
-<Xref>PMID:18406324</Xref>
-<Note>X-ray diffraction, 2.50 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Harms, J.M.</Author>
-<Author>Wilson, D.N.</Author>
-<Author>Schluenzen, F.</Author>
-<Author>Connell, S.R.</Author>
-<Author>Stachelhaus, T.</Author>
-<Author>Zaborowska, Z.</Author>
-<Author>Spahn, C.M.</Author>
-<Author>Fucini, P.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, March 2008</Citation>
-<Description>Thiopeptide antibiotic nosiheptide bound to the large ribosomal subunit of Deinococcus radiodurans.</Description>
-<Xref>PDB:2ZJP</Xref>
-<Note>X-ray diffraction, 3.70 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yu, Y.</Author>
-<Author>Duan, L.</Author>
-<Author>Zhang, Q.</Author>
-<Author>Liao, R.</Author>
-<Author>Ding, Y.</Author>
-<Author>Pan, H.</Author>
-<Author>Wendt-Pienkowski, E.</Author>
-<Author>Tang, G.</Author>
-<Author>Shen, B.</Author>
-<Author>Liu, W.</Author>
-</Authors>
-<Citation>ACS Chem. Biol. 4, 855-864, 2009</Citation>
-<Title>Nosiheptide biosynthesis featuring a unique indole side ring formation on the characteristic thiopeptide framework.</Title>
-<Xref>DOI:10.1021/cb900133x</Xref>
-<Xref>PMID:19678698</Xref>
-</ReferenceBlock>
-<Comment>This modification is currently represented in the PDB as part of the HET group for the entire molecule of nosiheptide.</Comment>
-<SequenceCode>
-<SequenceSpec>C, E</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Condition>incidental to RESID:AA0487</Condition>
-<Condition>incidental to RESID:AA0541</Condition>
-<Xref>PSI-MOD:01435</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="binding__3-methyl-4-hydroxymethylindole-2-carboxylic acid (covalent; via 2 links)__">BINDING 3-methyl-4-hydroxymethylindole-2-carboxylic acid (covalent; via 2 links)</Feature>
-</Features>
-<Image src="/images/AA0488.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0488.PDB" />
-</Entry>
-<Entry id="AA0489">
-<Header>
-<Code>AA0489</Code>
-<Dates>
-<CreationDate>31-Mar-2009</CreationDate>
-<StrucRevDate>31-Mar-2009</StrucRevDate>
-<TextChngDate>24-Aug-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>cyclo[(prolylserin)-O-yl] cysteinate</Name>
-<AlternateName>(3,6-dioxopyrrolo[4,5-a]piperazin-2-yl)methyl cysteinate</AlternateName>
-<SystematicName>[(3S,8aS)-1,4-dioxooctahydropyrrolo[1,2-a]pyrazin-3-yl]methyl (2R)-2-amino-3-sulfanylpropanoate</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 11 H 16 N 3 O 4 S 1</Formula>
-<Weight type="chemical">286.33</Weight>
-<Weight type="physical">286.086152</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005" label="CYS">
-<Formula>C 8 H 10 N 2 O 2 S 0</Formula>
-<Weight type="chemical">166.18</Weight>
-<Weight type="physical">166.074228</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0005 AA0015 AA0016" label="TRI">
-<Formula>C 0 H -2 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Shimanaka, K.</Author>
-<Author>Takahashi, Y.</Author>
-<Author>Iinuma, H.</Author>
-<Author>Naganawa, H.</Author>
-<Author>Takeuchi, T.</Author>
-</Authors>
-<Citation>J. Antibiot. 47, 1153-1159, 1994</Citation>
-<Title>Novel antibiotics, amythiamicins. III. Structure elucidations of amythiamicins A, B and C.</Title>
-<Xref>PMID:7961166</Xref>
-</ReferenceBlock>
-<Comment>This diketopiperazine ester is formed by cyclization of the C-terminal seryl-proline dipeptide and transesterification to cysteine.</Comment>
-<Comment>Although it is constructed from three C-terminal amino acids, for simplicity it is represented in the UniProt feature as a modification of cysteine and not as a crosslink.</Comment>
-<SequenceCode link="CYS">
-<SequenceSpec>C</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>PSI-MOD:01436</Xref>
-</SequenceCode>
-<SequenceCode link="TRI">
-<SequenceSpec>C, P, S</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Condition>cross-link 3</Condition>
-<Xref>PSI-MOD:01437</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>diketopiperazine ring</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__cyclo[(prolylserin)-o-yl] cysteinate__c">MOD_RES Cyclo[(prolylserin)-O-yl] cysteinate</Feature>
-</Features>
-<Image src="/images/AA0489.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0489.PDB" />
-</Entry>
-<Entry id="AA0490">
-<Header>
-<Code>AA0490</Code>
-<Dates>
-<CreationDate>12-Jun-2009</CreationDate>
-<StrucRevDate>12-Jun-2009</StrucRevDate>
-<TextChngDate>12-Jun-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>3-(O4'-L-tyrosyl)-L-valine</Name>
-<SystematicName>(2S)-2-amino-3-(4-[(2S)-2-amino-2-carboxyethyl]phenoxy)-3-methylbutanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 14 H 16 N 2 O 3</Formula>
-<Weight type="chemical">260.29</Weight>
-<Weight type="physical">260.116092</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0019 AA0020">
-<Formula>C 0 H -2 N 0 O 0</Formula>
-<Weight type="chemical">-2.02</Weight>
-<Weight type="physical">-2.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Andersson, C.S.</Author>
-<Author>Högbom, M.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 106, 5633-5638, 2009</Citation>
-<Title>A Mycobacterium tuberculosis ligand-binding Mn/Fe protein reveals a new cofactor in a remodeled R2-protein scaffold.</Title>
-<Xref>DOI:10.1073/pnas.0812971106</Xref>
-<Xref>PMID:19321420</Xref>
-<Note>X-ray diffraction, 1.90 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Andersson, C.S.</Author>
-<Author>Jones, T.A.</Author>
-<Author>Hogbom, M.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, September 2008</Citation>
-<Description>R2-like ligand binding Mn/Fe oxidase from M. tuberculosis.</Description>
-<Xref>PDB:3EE4</Xref>
-<Note>X-ray diffraction, 1.90 angstroms</Note>
-</ReferenceBlock>
-<Comment>This cross-link may be formed by a free-radical process during maturation of a metal cluster.</Comment>
-<SequenceCode>
-<SequenceSpec>V, Y</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Condition>incidental to RESID:AA0491</Condition>
-<Xref>PSI-MOD:01442</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="crosslnk__3-(o4'-tyrosyl)-valine (val-tyr)__v__y">CROSSLNK 3-(O4'-tyrosyl)-valine (Val-Tyr)</Feature>
-</Features>
-<Image src="/images/AA0490.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0490.PDB" />
-</Entry>
-<Entry id="AA0491">
-<Header>
-<Code>AA0491</Code>
-<Dates>
-<CreationDate>12-Jun-2009</CreationDate>
-<StrucRevDate>12-Jun-2009</StrucRevDate>
-<TextChngDate>31-Dec-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>tetrakis-L-glutamato bis-L-N1'-histidino lipid carboxylato manganese iron oxide</Name>
-</Names>
-<FormulaBlock>
-<Formula>C 46 Fe 1 H 65 Mn 1 N 10 O 17</Formula>
-<FormalCharge>1-</FormalCharge>
-<Weight type="chemical">1140.86</Weight>
-<Weight type="physical">1140.326447</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0006 AA0006 AA0006 AA0006 AA0009 AA0009">
-<Formula>C 14 Fe 1 H 23 Mn 1 N 0 O 3</Formula>
-<FormalCharge>1-</FormalCharge>
-<Weight type="chemical">350.12</Weight>
-<Weight type="physical">350.038251</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Andersson, C.S.</Author>
-<Author>Högbom, M.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 106, 5633-5638, 2009</Citation>
-<Title>A Mycobacterium tuberculosis ligand-binding Mn/Fe protein reveals a new cofactor in a remodeled R2-protein scaffold.</Title>
-<Xref>DOI:10.1073/pnas.0812971106</Xref>
-<Xref>PMID:19321420</Xref>
-<Note>X-ray diffraction, 1.90 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Andersson, C.S.</Author>
-<Author>Jones, T.A.</Author>
-<Author>Hogbom, M.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, September 2008</Citation>
-<Description>R2-like ligand binding Mn/Fe oxidase from M. tuberculosis.</Description>
-<Xref>PDB:3EE4</Xref>
-<Note>X-ray diffraction, 1.90 angstroms</Note>
-</ReferenceBlock>
-<Comment>It is not clear whether the lipid carboxylate is a cofactor or a substrate, and its identity is not certain. It was modeled as myristic acid.</Comment>
-<SequenceCode>
-<SequenceSpec>E, E, E, E, H, H</SequenceSpec>
-<Condition>cross-link 6</Condition>
-<Condition>incidental to RESID:AA0490</Condition>
-<Xref>PSI-MOD:01443</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>iron</Keyword>
-<Keyword>lipoprotein</Keyword>
-<Keyword>manganese</Keyword>
-<Keyword>metalloprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="metal__iron__e">METAL Iron</Feature>
-<Feature type="UniProt" key="metal__iron; via pros nitrogen__h">METAL Iron; via pros nitrogen</Feature>
-<Feature type="UniProt" key="metal__manganese__e">METAL Manganese</Feature>
-<Feature type="UniProt" key="metal__manganese; via pros nitrogen__h">METAL Manganese; via pros nitrogen</Feature>
-</Features>
-<Image src="/images/AA0491.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0491.PDB" />
-</Entry>
-<Entry id="AA0492">
-<Header>
-<Code>AA0492</Code>
-<Dates>
-<CreationDate>12-Jun-2009</CreationDate>
-<StrucRevDate>12-Jun-2009</StrucRevDate>
-<TextChngDate>30-Sep-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>3,3-dihydroxy-L-alanine</Name>
-<AlternateName>2-(dihydroxymethyl)glycine</AlternateName>
-<AlternateName>3,3-dihydroxyalanine</AlternateName>
-<AlternateName>3-hydroxy-L-serine</AlternateName>
-<AlternateName>3-oxoalanine hydrate</AlternateName>
-<AlternateName>C(alpha)-formylglycine hydrate [misnomer]</AlternateName>
-<SystematicName>(S)-2-amino-3,3-dihydroxypropanoic acid</SystematicName>
-<Xref>PDBHET:DDZ</Xref>
-<Xref>PDBHET:FGL</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 5 N 1 O 3</Formula>
-<Weight type="chemical">103.08</Weight>
-<Weight type="physical">103.026943</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005" label="CYS">
-<Formula>C 0 H 0 N 0 O 2 S -1</Formula>
-<Weight type="chemical">-0.06</Weight>
-<Weight type="physical">0.017758</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0016" label="SER">
-<Formula>C 0 H 0 N 0 O 1</Formula>
-<Weight type="chemical">16.00</Weight>
-<Weight type="physical">15.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Jackson, W.G.</Author>
-<Author>McLaughlin, G.M.</Author>
-<Author>Sargeson, A.M.</Author>
-<Author>Watson, A.D.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 105, 2426-2430, 1983</Citation>
-<Title>Synthesis, molecular structure and chemistry of p-[CoIII(tren)(2-(dihydroxymethyl)glycinato)]ZnCl4.2H2O.</Title>
-<Xref>DOI:10.1021/ja00346a052</Xref>
-<Note>chemical synthesis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Waldow, A.</Author>
-<Author>Schmidt, B.</Author>
-<Author>Dierks, T.</Author>
-<Author>von Bülow, R.</Author>
-<Author>von Figura, K.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 274, 12284-12288, 1999</Citation>
-<Title>Amino acid residues forming the active site of arylsulfatase A. Role in catalytic activity and substrate binding.</Title>
-<Xref>DOI:10.1074/jbc.274.18.12284</Xref>
-<Xref>PMID:10212197</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Boltes, I.</Author>
-<Author>Czapinska, H.</Author>
-<Author>Kahnert, A.</Author>
-<Author>von Bülow, R.</Author>
-<Author>Dierks, T.</Author>
-<Author>Schmidt, B.</Author>
-<Author>von Figura, K.</Author>
-<Author>Kertesz, M.A.</Author>
-<Author>Usón, I.</Author>
-</Authors>
-<Citation>Structure 9, 483-491, 2001</Citation>
-<Title>1.3 A structure of arylsulfatase from Pseudomonas aeruginosa establishes the catalytic mechanism of sulfate ester cleavage in the sulfatase family.</Title>
-<Xref>DOI:10.1016/S0969-2126(01)00609-8</Xref>
-<Xref>PMID:11435113</Xref>
-<Note>X-ray diffraction, 1.3 angstroms; the active site residue is shown as a gem-diol and referred to as a "formylglycine hydrate"</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Boltes, I.</Author>
-<Author>Czapinska, H.</Author>
-<Author>Kahnert, A.</Author>
-<Author>von Buelow, R.</Author>
-<Author>Dierks, T.</Author>
-<Author>Schmidt, B.</Author>
-<Author>von Figura, K.</Author>
-<Author>Kertesz, M.A.</Author>
-<Author>Uson, I.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, November 2000</Citation>
-<Description>Arylsulfatase from Pseudomonas aeruginosa.</Description>
-<Xref>PDB:1HDH</Xref>
-<Note>X-ray diffraction, 1.3 angstroms; the depositors refer to the modified residue as "formylglycine hydrate", but it is incorrectly annotated as FGL, 2-aminopropanedioic acid</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ghosh, D.</Author>
-</Authors>
-<Citation>Cell. Mol. Life Sci. 64, 2013-2022, 2007</Citation>
-<Title>Human sulfatases: a structural perspective to catalysis.</Title>
-<Xref>DOI:10.1007/s00018-007-7175-y</Xref>
-<Xref>PMID:17558559</Xref>
-<Note>review article discussing the functioning of the dihydroxymethyl group in the active site</Note>
-</ReferenceBlock>
-<Comment>This active site residue is formed by the spontaneous hydration of the aldehyde, 2-amino-3oxopropanoic acid. See RESID:AA0185.</Comment>
-<Comment>The PDB hetgroup FGL was originally designated as the "C(alpha)-formyl glycine" active site residue L-3-oxoalanine observed in its hydrated form. That structure, a gem-diol with an sp(3) carbon, was misinterpreted as a carboxyl with an sp(2) carbon, and assigned to aminomalonic acid (see RESID:AA0458) instead. The hetgroup DDZ is being introduced for 3,3-dihydroxyalanine.</Comment>
-<GeneratingEnzyme>
-<EnzymeName link="SER">sulfatase maturing enzyme (sulfatase modifying factor, C-alpha-formylglycine-generating enzyme) (EC 1.1.99.-)</EnzymeName>
-<EnzymeName link="CYS">sulfatase maturing enzyme (sulfatase modifying factor, C-alpha-formylglycine-generating enzyme) (EC 1.8.99.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode link="CYS">
-<SequenceSpec>C</SequenceSpec>
-<Xref>PSI-MOD:01444</Xref>
-<Xref>PSI-MOD:01448</Xref>
-</SequenceCode>
-<SequenceCode link="SER">
-<SequenceSpec>S</SequenceSpec>
-<Xref>PSI-MOD:01445</Xref>
-<Xref>PSI-MOD:01448</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not currently annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0492.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0492.PDB" />
-</Entry>
-<Entry id="AA0493">
-<Header>
-<Code>AA0493</Code>
-<Dates>
-<CreationDate>12-Jun-2009</CreationDate>
-<StrucRevDate>12-Jun-2009</StrucRevDate>
-<TextChngDate>30-Sep-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-(dihydroxymethyl)-L-methionine</Name>
-<AlternateName>N-formyl-L-methionine hydrate</AlternateName>
-<AlternateName>N-orthoformylmethionine</AlternateName>
-<SystematicName>(2S)-2-[(dihydroxymethyl)amino]-4-(methylsulfanyl)butanoic acid</SystematicName>
-<Xref>PDBHET:CXM</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 12 N 1 O 3 S 1</Formula>
-<Weight type="chemical">178.23</Weight>
-<Weight type="physical">178.053789</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0021" label="FMET">
-<Formula>C 0 H 2 N 0 O 1 S 0</Formula>
-<Weight type="chemical">18.02</Weight>
-<Weight type="physical">18.010565</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0013" label="MET">
-<Formula>C 1 H 2 N 0 O 2 S 0</Formula>
-<Weight type="chemical">46.03</Weight>
-<Weight type="physical">46.005479</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Prince, S.M.</Author>
-<Author>Papiz, M.Z.</Author>
-<Author>Freer, A.A.</Author>
-<Author>McDermott, G.</Author>
-<Author>Hawthornthwaite-Lawless, A.M.</Author>
-<Author>Cogdell, R.J.</Author>
-<Author>Isaacs, N.W.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 268, 412-423, 1997</Citation>
-<Title>Apoprotein structure in the LH2 complex from Rhodopseudomonas acidophila strain 10050: modular assembly and protein pigment interactions.</Title>
-<Xref>DOI:10.1006/jmbi.1997.0966</Xref>
-<Xref>PMID:9159480</Xref>
-<Note>X-ray diffraction, 2.50 angstroms; an N-formyl carbonyl group axially ligates the magnesium ion of bacteriochlorophyll a in light-harvesting protein B-800/850 alpha chain</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Cogdell, R.J.</Author>
-<Author>Freer, A.A.</Author>
-<Author>Isaacs, N.W.</Author>
-<Author>Hawthornthwaite-Lawless, A.M.</Author>
-<Author>McDermott, G.</Author>
-<Author>Papiz, M.Z.</Author>
-<Author>Prince, S.M.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, August 1996</Citation>
-<Description>Integral membrane peripheral light harvesting complex from Rhodopseudomonas acidophila strain 10050.</Description>
-<Xref>PDB:1KZU</Xref>
-<Note>X-ray diffraction, 2.50 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Papiz, M.Z.</Author>
-<Author>Prince, S.M.</Author>
-<Author>Howard, T.</Author>
-<Author>Cogdell, R.J.</Author>
-<Author>Isaacs, N.W.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 326, 1523-1538, 2003</Citation>
-<Title>The structure and thermal motion of the B800-850 LH2 complex from Rps. acidophila at 2.0 angstroms resolution and 100 K: new structural features and functionally relevant motions.</Title>
-<Xref>DOI:10.1016/S0022-2836(03)00024-X</Xref>
-<Xref>PMID:12595263</Xref>
-<Note>X-ray diffraction, 2.0 angstroms; the formyl group ligand is remodeled with two oxygens as a carboxyl group, but appears to be tetrahedral rather than trigonal planar</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Papiz, M.Z.</Author>
-<Author>Prince, S.M.</Author>
-<Author>Howard, T.</Author>
-<Author>Cogdell, R.J.</Author>
-<Author>Isaacs, N.W.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, January 2003</Citation>
-<Description>Crystal structure of LH2 B800-850 from Rps. acidophila at 2.0 Angstrom resolution.</Description>
-<Xref>PDB:1NKZ</Xref>
-<Note>X-ray diffraction, 2.00 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Demirci, H.</Author>
-<Author>Larsen, L.H.</Author>
-<Author>Hansen, T.</Author>
-<Author>Rasmussen, A.</Author>
-<Author>Cadambi, A.</Author>
-<Author>Gregory, S.T.</Author>
-<Author>Kirpekar, F.</Author>
-<Author>Jogl, G.</Author>
-</Authors>
-<Citation>RNA 16, 1584-1596, 2010</Citation>
-<Title>Multi-site-specific 16S rRNA methyltransferase RsmF from Thermus thermophilus.</Title>
-<Xref>DOI:10.1261/rna.2088310</Xref>
-<Xref>PMID:20558545</Xref>
-<Note>X-ray diffraction, 1.68 angstroms; the N-formylmethionine group observed with extra density is interpreted as N-(dihydroxymethyl)-L-methionine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Demirci, H.</Author>
-<Author>Larsen, L.H.</Author>
-<Author>Hansen, T.</Author>
-<Author>Rasmussen, A.</Author>
-<Author>Cadambi, A.</Author>
-<Author>Gregory, S.T.</Author>
-<Author>Kirpekar, F.</Author>
-<Author>Jogl, G.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, March 2010</Citation>
-<Description>Multi-site-specific 16S rRNA methyltransferase RsmF from Thermus thermophilus in space group P21212.</Description>
-<Xref>PDB:3M6X</Xref>
-<Note>X-ray diffraction, 1.68 angstroms</Note>
-</ReferenceBlock>
-<Comment>The formyl group of N-formylmethionine, as an aldehyde, may undergo spontaneous addition of water to form a dihydoxymethyl group. It is detectable by mass spectrometry and other methods.</Comment>
-<Comment>Although appropriate, the keyword "thioether bond" normally does not appear for this amino acid.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>methionine--tRNA ligase (EC 6.1.1.10)</EnzymeName>
-<EnzymeName>methionyl-tRNA formyltransferase (EC 2.1.2.9)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode link="FMET">
-<SequenceSpec>M</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>PSI-MOD:01446</Xref>
-</SequenceCode>
-<SequenceCode link="MET">
-<SequenceSpec>M</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>PSI-MOD:01447</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>*thioether bond</Keyword>
-<Keyword>blocked amino end</Keyword>
-<Keyword>formylation</Keyword>
-<Keyword>pretranslational modification</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not currently annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0493.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0493.PDB" />
-</Entry>
-<Entry id="AA0494">
-<Header>
-<Code>AA0494</Code>
-<Dates>
-<CreationDate>30-Jun-2009</CreationDate>
-<StrucRevDate>30-Jun-2009</StrucRevDate>
-<TextChngDate>31-Mar-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-(DNA-1',2'-dideoxyribos-1'-ylidene)-L-prolinium</Name>
-<AlternateName>DNA glycosylase proline Schiff base intermediate [misnomer]</AlternateName>
-<SystematicName>(1Z,2S)-2-carboxy-1-[(3R,4R)-3,4-dihydroxy-5-(phosphonooxy)pentylidene]pyrrolidinium</SystematicName>
-<Xref>PDBHET:PED</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 10 H 16 N 1 O 6 P 1 +</Formula>
-<FormalCharge>1+</FormalCharge>
-<Weight type="chemical">277.21 +</Weight>
-<Weight type="physical">277.070975 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0015">
-<Formula>C 5 H 8 N 0 O 5 P 1 +</Formula>
-<FormalCharge>1+</FormalCharge>
-<Weight type="chemical">179.09 +</Weight>
-<Weight type="physical">179.010386 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Zharkov, D.O.</Author>
-<Author>Rieger, R.A.</Author>
-<Author>Iden, C.R.</Author>
-<Author>Grollman, A.P.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 272, 5335-5341, 1997</Citation>
-<Title>NH2-terminal proline acts as a nucleophile in the glycosylase/AP-lyase reaction catalyzed by Escherichia coli formamidopyrimidine-DNA glycosylase (Fpg) protein.</Title>
-<Xref>DOI:10.1074/jbc.272.8.5335</Xref>
-<Xref>PMID:9030608</Xref>
-<Note>chemical identification and characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Rieger, R.A.</Author>
-<Author>McTigue, M.M.</Author>
-<Author>Kycia, J.H.</Author>
-<Author>Gerchman, S.E.</Author>
-<Author>Grollman, A.P.</Author>
-<Author>Iden, C.R.</Author>
-</Authors>
-<Citation>J. Am. Soc. Mass Spectrom. 11, 505-515, 2000</Citation>
-<Title>Characterization of a cross-linked DNA-endonuclease VIII repair complex by electrospray ionization mass spectrometry.</Title>
-<Xref>DOI:10.1016/S1044-0305(00)00117-3</Xref>
-<Xref>PMID:10833024</Xref>
-<Note>mass spectrometric detection and linkage analysis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Zharkov, D.O.</Author>
-<Author>Golan, G.</Author>
-<Author>Gilboa, R.</Author>
-<Author>Fernandes, A.S.</Author>
-<Author>Gerchman, S.E.</Author>
-<Author>Kycia, J.H.</Author>
-<Author>Rieger, R.A.</Author>
-<Author>Grollman, A.P.</Author>
-<Author>Shoham, G.</Author>
-</Authors>
-<Citation>EMBO J. 21, 789-800, 2002</Citation>
-<Title>Structural analysis of an Escherichia coli endonuclease VIII covalent reaction intermediate.</Title>
-<Xref>DOI:10.1093/emboj/21.4.789</Xref>
-<Xref>PMID:11847126</Xref>
-<Note>X-ray diffraction, 1.25 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Golan, G.</Author>
-<Author>Zharkov, D.O.</Author>
-<Author>Gilboa, R.</Author>
-<Author>Fernandes, A.S.</Author>
-<Author>Kycia, J.H.</Author>
-<Author>Gerchman, S.E.</Author>
-<Author>Rieger, R.A.</Author>
-<Author>Grollman, A.P.</Author>
-<Author>Shoham, G.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, October 2001</Citation>
-<Description>Crystal structure of a trapped reaction intermediate of the DNA repair enzyme endonuclease VIII with DNA.</Description>
-<Xref>PDB:1KZU</Xref>
-<Note>X-ray diffraction, 1.42 angstroms</Note>
-</ReferenceBlock>
-<Comment>The modification is frequently referred to as a "Schiff base". As an iminium bonded to three carbons, this is not a Schiff base, defined in the IUPAC Compendium of Chemical Terminology, 2nd ed. ("the Gold Book", http://goldbook.iupac.org/index.html) as an imine (uncharged, double bonded nitrogen) bonded to two carbons. Chemically it is not a "base" because it cannot act as either a proton acceptor (a "Brønsted-Lowry base") or as an electron pair donor (a "Lewis base").</Comment>
-<Comment>The model has three open valences, one on the proline carboxyl group and two in the DNA nucleotide segment on the 5'-phosphate and the 3'-hydroxyl.</Comment>
-<Comment>The keyword "phosphoprotein" is not used with polynucleotide-linked intermediate modifications.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>formamidopyrimidine-DNA glycosylase (EC 3.2.2.23)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>P</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>PSI-MOD:01454</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>*phosphoprotein</Keyword>
-<Keyword>blocked amino end</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt" key="act_site__schiff-base intermediate with dna__p">ACT_SITE Schiff-base intermediate with DNA</Feature>
-<Note>this UniProt feature has a structural misrepresentation</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0494.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0494.PDB" />
-</Entry>
-<Entry id="AA0495">
-<Header>
-<Code>AA0495</Code>
-<Dates>
-<CreationDate>28-Aug-2009</CreationDate>
-<StrucRevDate>28-Aug-2009</StrucRevDate>
-<TextChngDate>30-Sep-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-(glycyl)-L-serine</Name>
-<AlternateName>O3-(aminoacetyl)serine</AlternateName>
-<AlternateName>serine glycinate ester</AlternateName>
-<SystematicName>(2S)-2-amino-3-[(aminoacetyl)oxy]propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 7 N 2 O 3</Formula>
-<Weight type="chemical">143.12</Weight>
-<Weight type="physical">143.045667</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0008 AA0016">
-<Formula>C 0 H -2 N 0 O -1</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wang, X.</Author>
-<Author>Herr, R.A.</Author>
-<Author>Chua, W.J.</Author>
-<Author>Lybarger, L.</Author>
-<Author>Wiertz, E.J.</Author>
-<Author>Hansen, T.H.</Author>
-</Authors>
-<Citation>J. Cell Biol. 177, 613-624, 2007</Citation>
-<Title>Ubiquitination of serine, threonine, or lysine residues on the cytoplasmic tail can induce ERAD of MHC-I by viral E3 ligase mK3.</Title>
-<Xref>DOI:10.1083/jcb.200611063</Xref>
-<Xref>PMID:17502423</Xref>
-<Note>chemical and directed mutation analysis</Note>
-</ReferenceBlock>
-<Comment>These are ester cross-links formed between internal serine residues and the carboxyl end of ubiquitin and other proteins.</Comment>
-<SequenceCode>
-<SequenceSpec>G, S</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:01585</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__glycyl serine ester (ser-gly) (interchain with g-cter__s">CROSSLNK Glycyl serine ester (Ser-Gly) (interchain with G-Cter ...)</Feature>
-</Features>
-<Image src="/images/AA0495.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0495.PDB" />
-</Entry>
-<Entry id="AA0496">
-<Header>
-<Code>AA0496</Code>
-<Dates>
-<CreationDate>28-Aug-2009</CreationDate>
-<StrucRevDate>28-Aug-2009</StrucRevDate>
-<TextChngDate>30-Sep-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-(glycyl)-L-threonine</Name>
-<AlternateName>O3-(2-aminoacetyl)threonine</AlternateName>
-<AlternateName>threonine glycinate ester</AlternateName>
-<SystematicName>(2S,3R)-2-amino-3-[(aminoacetyl)oxy]butanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 9 N 2 O 3</Formula>
-<Weight type="chemical">157.15</Weight>
-<Weight type="physical">157.061317</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0008 AA0017">
-<Formula>C 0 H -2 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wang, X.</Author>
-<Author>Herr, R.A.</Author>
-<Author>Chua, W.J.</Author>
-<Author>Lybarger, L.</Author>
-<Author>Wiertz, E.J.</Author>
-<Author>Hansen, T.H.</Author>
-</Authors>
-<Citation>J. Cell Biol. 177, 613-624, 2007</Citation>
-<Title>Ubiquitination of serine, threonine, or lysine residues on the cytoplasmic tail can induce ERAD of MHC-I by viral E3 ligase mK3.</Title>
-<Xref>DOI:10.1083/jcb.200611063</Xref>
-<Xref>PMID:17502423</Xref>
-<Note>chemical and directed mutation analysis</Note>
-</ReferenceBlock>
-<Comment>These are ester cross-links formed between internal threonine residues and the carboxyl end of ubiquitin and other proteins.</Comment>
-<SequenceCode>
-<SequenceSpec>G, T</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:01586</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__glycyl threonine ester (thr-gly) (interchain with g-cter__t">CROSSLNK Glycyl threonine ester (Thr-Gly) (interchain with G-Cter ...)</Feature>
-</Features>
-<Image src="/images/AA0496.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0496.PDB" />
-</Entry>
-<Entry id="AA0497">
-<Header>
-<Code>AA0497</Code>
-<Dates>
-<CreationDate>28-Aug-2009</CreationDate>
-<StrucRevDate>28-Aug-2009</StrucRevDate>
-<TextChngDate>28-Aug-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-(2-aminoethylphosphoryl)-L-serine</Name>
-<AlternateName>O3-(2-aminoethylphosphoryl)-L-serine</AlternateName>
-<AlternateName>O3-(phosphoethanolamine)-L-serine</AlternateName>
-<AlternateName>serine ethanolamine phosphate</AlternateName>
-<AlternateName>serine ethanolamine phosphodiester</AlternateName>
-<SystematicName>(2S)-2-amino-3-([(2-aminoethoxy)(hydroxy)phosphoryl]oxy)propanoic acid</SystematicName>
-<Xref>CAS:1186-34-1</Xref>
-<Xref>PDBHET:OPE</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 11 N 2 O 5 P 1</Formula>
-<Weight type="chemical">210.13</Weight>
-<Weight type="physical">210.040558</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 2 H 6 N 1 O 3 P 1</Formula>
-<Weight type="chemical">123.05</Weight>
-<Weight type="physical">123.008530</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hegge, F.T.</Author>
-<Author>Hitchen, P.G.</Author>
-<Author>Aas, F.E.</Author>
-<Author>Kristiansen, H.</Author>
-<Author>Løvold, C.</Author>
-<Author>Egge-Jacobsen, W.</Author>
-<Author>Panico, M.</Author>
-<Author>Leong, W.Y.</Author>
-<Author>Bull, V.</Author>
-<Author>Virji, M.</Author>
-<Author>Morris, H.R.</Author>
-<Author>Dell, A.</Author>
-<Author>Koomey, M.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 101, 10798-10803, 2004</Citation>
-<Title>Unique modifications with phosphocholine and phosphoethanolamine define alternate antigenic forms of Neisseria gonorrhoeae type IV pili.</Title>
-<Xref>DOI:10.1073/pnas.0402397101</Xref>
-<Xref>PMID:15249686</Xref>
-<Note>mass spectrometric detection</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Aas, F.E.</Author>
-<Author>Egge-Jacobsen, W.</Author>
-<Author>Winther-Larsen, H.C.</Author>
-<Author>Løvold, C.</Author>
-<Author>Hitchen, P.G.</Author>
-<Author>Dell, A.</Author>
-<Author>Koomey, M.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 281, 27712-27723, 2006</Citation>
-<Title>Neisseria gonorrhoeae type IV pili undergo multisite, hierarchical modifications with phosphoethanolamine and phosphocholine requiring an enzyme structurally related to lipopolysaccharide phosphoethanolamine transferases.</Title>
-<Xref>DOI:10.1074/jbc.M604324200</Xref>
-<Xref>PMID:16825186</Xref>
-<Note>mass spectrometric identification, directed mutation analysis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Craig, L.</Author>
-<Author>Volkmann, N.</Author>
-<Author>Arvai, A.S.</Author>
-<Author>Pique, M.E.</Author>
-<Author>Yeager, M.</Author>
-<Author>Egelman, E.H.</Author>
-<Author>Tainer, J.A.</Author>
-</Authors>
-<Citation>Mol. Cell 23, 651-662, 2006</Citation>
-<Title>Type IV pilus structure by cryo-electron microscopy and crystallography: implications for pilus assembly and functions.</Title>
-<Xref>DOI:10.1016/j.molcel.2006.07.004</Xref>
-<Xref>PMID:16949362</Xref>
-<Note>X-ray diffraction, 2.30 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Craig, L.</Author>
-<Author>Volkmann, N.</Author>
-<Author>Arvai, A.S.</Author>
-<Author>Pique, M.E.</Author>
-<Author>Yeager, M.</Author>
-<Author>Egelman, E.H.</Author>
-<Author>Tainer, J.A.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, June 2006</Citation>
-<Description>Crystal structure of native Neisseria gonorrhoeae type IV pilin at 2.3 Angstroms resolution.</Description>
-<Xref>PDB:2HI2</Xref>
-<Note>X-ray diffraction, 2.30 angstroms</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>PSI-MOD:01587</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__o-(2-aminoethylphosphoryl)serine__s">MOD_RES O-(2-aminoethylphosphoryl)serine</Feature>
-</Features>
-<Image src="/images/AA0497.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0497.PDB" />
-</Entry>
-<Entry id="AA0498">
-<Header>
-<Code>AA0498</Code>
-<Dates>
-<CreationDate>28-Aug-2009</CreationDate>
-<StrucRevDate>28-Aug-2009</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-cholinephosphoryl-L-serine</Name>
-<AlternateName>2-[([(2S)-2-azanyl-2-carboxyethoxy][hydroxy]phosphoryl)oxy]-N,N,N-trimethylethanazanium</AlternateName>
-<AlternateName>O3-phosphocholine-L-serine</AlternateName>
-<AlternateName>O3-[(2-[trimethylammonio]ethyl)phosphoryl]-L-serine</AlternateName>
-<AlternateName>serine choline phosphate</AlternateName>
-<AlternateName>serine choline phosphodiester</AlternateName>
-<SystematicName>2-[([(2S)-2-amino-2-carboxyethoxy][hydroxy]phosphoryl)oxy]-N,N,N-trimethylethanaminium</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 8 H 18 N 2 O 5 P 1</Formula>
-<FormalCharge>1+</FormalCharge>
-<Weight type="chemical">253.21</Weight>
-<Weight type="physical">253.094785</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 5 H 13 N 1 O 3 P 1</Formula>
-<FormalCharge>1+</FormalCharge>
-<Weight type="chemical">166.14</Weight>
-<Weight type="physical">166.062756</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hegge, F.T.</Author>
-<Author>Hitchen, P.G.</Author>
-<Author>Aas, F.E.</Author>
-<Author>Kristiansen, H.</Author>
-<Author>Løvold, C.</Author>
-<Author>Egge-Jacobsen, W.</Author>
-<Author>Panico, M.</Author>
-<Author>Leong, W.Y.</Author>
-<Author>Bull, V.</Author>
-<Author>Virji, M.</Author>
-<Author>Morris, H.R.</Author>
-<Author>Dell, A.</Author>
-<Author>Koomey, M.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 101, 10798-10803, 2004</Citation>
-<Title>Unique modifications with phosphocholine and phosphoethanolamine define alternate antigenic forms of Neisseria gonorrhoeae type IV pili.</Title>
-<Xref>DOI:10.1073/pnas.0402397101</Xref>
-<Xref>PMID:15249686</Xref>
-<Note>mass spectrometric detection</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Aas, F.E.</Author>
-<Author>Egge-Jacobsen, W.</Author>
-<Author>Winther-Larsen, H.C.</Author>
-<Author>Løvold, C.</Author>
-<Author>Hitchen, P.G.</Author>
-<Author>Dell, A.</Author>
-<Author>Koomey, M.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 281, 27712-27723, 2006</Citation>
-<Title>Neisseria gonorrhoeae type IV pili undergo multisite, hierarchical modifications with phosphoethanolamine and phosphocholine requiring an enzyme structurally related to lipopolysaccharide phosphoethanolamine transferases.</Title>
-<Xref>DOI:10.1074/jbc.M604324200</Xref>
-<Xref>PMID:16825186</Xref>
-<Note>mass spectrometric identification, directed mutation analysis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Craig, L.</Author>
-<Author>Volkmann, N.</Author>
-<Author>Arvai, A.S.</Author>
-<Author>Pique, M.E.</Author>
-<Author>Yeager, M.</Author>
-<Author>Egelman, E.H.</Author>
-<Author>Tainer, J.A.</Author>
-</Authors>
-<Citation>Mol. Cell 23, 651-662, 2006</Citation>
-<Title>Type IV pilus structure by cryo-electron microscopy and crystallography: implications for pilus assembly and functions.</Title>
-<Xref>DOI:10.1016/j.molcel.2006.07.004</Xref>
-<Xref>PMID:16949362</Xref>
-<Note>X-ray diffraction, 2.3 angstroms; this modification is discussed but not modeled</Note>
-</ReferenceBlock>
-<Comment>In Neisseria this is produced as a secondary modification by methylation of O-(2-aminoethylphosphoryl)-L-serine. See RESID:AA0497.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>phosphocholine transferase AnkX (EC 2.7.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Condition>secondary to RESID:AA0497</Condition>
-<Xref>PSI-MOD:01588</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__o-(2-cholinephosphoryl)serine__s">MOD_RES O-(2-cholinephosphoryl)serine</Feature>
-</Features>
-<Image src="/images/AA0498.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0498.PDB" />
-</Entry>
-<Entry id="AA0499">
-<Header>
-<Code>AA0499</Code>
-<Dates>
-<CreationDate>28-Aug-2009</CreationDate>
-<StrucRevDate>28-Aug-2009</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-(2,4-diacetamido-2,4-dideoxy-D-glucosyl)-L-serine</Name>
-<AlternateName>DADDGlc</AlternateName>
-<AlternateName>O-(2,4-diacetamido-2,4-dideoxy-beta-D-glucopyranosyl)-L-serine</AlternateName>
-<AlternateName>O-seryl-beta-2,4-bis(acetylamino)glucoside</AlternateName>
-<AlternateName>O-[2,4-bis(acetylamino)]glucosyl-L-serine</AlternateName>
-<AlternateName>O3-(2,4-diacetamido-2,4-dideoxy-beta-D-glucopyranosyl)-L-serine</AlternateName>
-<SystematicName>(2S)-2-amino-3-[(2,4-diacetamido-2,4-dideoxy-beta-D-glucopyranosyl)oxy]propanoic acid</SystematicName>
-<Xref>PDBHET:DT6</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 13 H 21 N 3 O 7</Formula>
-<Weight type="chemical">331.33</Weight>
-<Weight type="physical">331.137950</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 10 H 16 N 2 O 5</Formula>
-<Weight type="chemical">244.25</Weight>
-<Weight type="physical">244.105922</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hegge, F.T.</Author>
-<Author>Hitchen, P.G.</Author>
-<Author>Aas, F.E.</Author>
-<Author>Kristiansen, H.</Author>
-<Author>Løvold, C.</Author>
-<Author>Egge-Jacobsen, W.</Author>
-<Author>Panico, M.</Author>
-<Author>Leong, W.Y.</Author>
-<Author>Bull, V.</Author>
-<Author>Virji, M.</Author>
-<Author>Morris, H.R.</Author>
-<Author>Dell, A.</Author>
-<Author>Koomey, M.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 101, 10798-10803, 2004</Citation>
-<Title>Unique modifications with phosphocholine and phosphoethanolamine define alternate antigenic forms of Neisseria gonorrhoeae type IV pili.</Title>
-<Xref>DOI:10.1073/pnas.0402397101</Xref>
-<Xref>PMID:15249686</Xref>
-<Note>mass spectrometric detection; reported as 2,4-diacetamido-2,4,6-trideoxyhexoside in Nesseria gonorrhoeae strain MS11</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Craig, L.</Author>
-<Author>Volkmann, N.</Author>
-<Author>Arvai, A.S.</Author>
-<Author>Pique, M.E.</Author>
-<Author>Yeager, M.</Author>
-<Author>Egelman, E.H.</Author>
-<Author>Tainer, J.A.</Author>
-</Authors>
-<Citation>Mol. Cell 23, 651-662, 2006</Citation>
-<Title>Type IV pilus structure by cryo-electron microscopy and crystallography: implications for pilus assembly and functions.</Title>
-<Xref>DOI:10.1016/j.molcel.2006.07.004</Xref>
-<Xref>PMID:16949362</Xref>
-<Note>X-ray diffraction, 2.30 angstroms, cryoelectron microscopy, 12.5 angstroms; the modification is not chemically characterized</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Craig, L.</Author>
-<Author>Volkmann, N.</Author>
-<Author>Arvai, A.S.</Author>
-<Author>Pique, M.E.</Author>
-<Author>Yeager, M.</Author>
-<Author>Egelman, E.H.</Author>
-<Author>Tainer, J.A.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, June 2006</Citation>
-<Description>Crystal structure of native Neisseria gonorrhoeae type IV pilin at 2.3 Angstroms resolution.</Description>
-<Xref>PDB:2HI2</Xref>
-<Note>X-ray diffraction, 2.30 angstroms</Note>
-</ReferenceBlock>
-<Comment>It is not clear whether or not there is a chemical difference in the glycosylation of the two varieties of strain MS11 used in these experiments.</Comment>
-<Comment>For O-(2,4-diacetamido-2,4,6-trideoxy-D-glucosyl)-L-serine, see RESID:AA0607.</Comment>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>PSI-MOD:01589</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__o-linked (daddglc...) serine__s">CARBOHYD O-linked (DADDGlc...) serine</Feature>
-</Features>
-<Image src="/images/AA0499.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0499.PDB" />
-</Entry>
-<Entry id="AA0500">
-<Header>
-<Code>AA0500</Code>
-<Dates>
-<CreationDate>28-Aug-2009</CreationDate>
-<StrucRevDate>28-Aug-2009</StrucRevDate>
-<TextChngDate>01-Mar-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>3'-farnesyl-2',3'-dihydro-2',N2-cyclo-L-tryptophan</Name>
-<SystematicName>(2S,3aR,8aS)-3a-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]-1,2,3,3a,8,8a-hexahydropyrrolo[2,3-b]indole-2-carboxylic acid</SystematicName>
-<Xref>ChEBI:52950</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 26 H 34 N 2 O 1</Formula>
-<Weight type="chemical">390.57</Weight>
-<Weight type="physical">390.267114</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0018">
-<Formula>C 15 H 24 N 0 O 0</Formula>
-<Weight type="chemical">204.36</Weight>
-<Weight type="physical">204.187801</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Okada, M.</Author>
-<Author>Yamaguchi, H.</Author>
-<Author>Sato, I.</Author>
-<Author>Tsuji, F.</Author>
-<Author>Dubnau, D.</Author>
-<Author>Sakagami, Y.</Author>
-</Authors>
-<Citation>Biosci. Biotechnol. Biochem. 72, 914-918, 2008</Citation>
-<Title>Chemical structure of posttranslational modification with a farnesyl group on tryptophan.</Title>
-<Xref>DOI:10.1271/bbb.80006</Xref>
-<Xref>PMID:18323630</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Okada, M.</Author>
-</Authors>
-<Citation>Biosci. Biotechnol. Biochem. 75, 1413-1417, 2011</Citation>
-<Title>Post-translational isoprenylation of tryptophan.</Title>
-<Xref>DOI:10.1271/bbb.110087</Xref>
-<Xref>PMID:21821957</Xref>
-<Note>review article</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>W</SequenceSpec>
-<Xref>PSI-MOD:01590</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lipoprotein</Keyword>
-<Keyword>prenylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__3&apos;-farnesyl-2&apos;,n2-cyclotryptophan__w">LIPID 3'-farnesyl-2',N2-cyclotryptophan</Feature>
-</Features>
-<Image src="/images/AA0500.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0500.PDB" />
-</Entry>
-<Entry id="AA0501">
-<Header>
-<Code>AA0501</Code>
-<Dates>
-<CreationDate>30-Sep-2009</CreationDate>
-<StrucRevDate>30-Sep-2009</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-(L-lysyl)-L-methionine sulfilimine</Name>
-<AlternateName>(E)-N6-([(3S)-3-amino-3-carboxypropyl](methyl)-lambda(4)-sulfanylidene)-L-lysine</AlternateName>
-<AlternateName>S-lysyl-methionine</AlternateName>
-<SystematicName>(2S)-2-amino-6-([(E)-[(3S)-3-amino-3-carboxypropyl](methyl)-lambda(4)-sulfanylidene]amino)hexanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 11 H 19 N 3 O 2 S 1</Formula>
-<Weight type="chemical">257.35</Weight>
-<Weight type="physical">257.119798</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012 AA0013">
-<Formula>C 0 H -2 N 0 O 0 S 0</Formula>
-<Weight type="chemical">-2.02</Weight>
-<Weight type="physical">-2.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Than, M.E.</Author>
-<Author>Henrich, S.</Author>
-<Author>Huber, R.</Author>
-<Author>Ries, A.</Author>
-<Author>Mann, K.</Author>
-<Author>Kühn, K.</Author>
-<Author>Timpl, R.</Author>
-<Author>Bourenkov, G.P.</Author>
-<Author>Bartunik, H.D.</Author>
-<Author>Bode, W.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 99, 6607-6612, 2002</Citation>
-<Title>The 1.9-A crystal structure of the noncollagenous (NC1) domain of human placenta collagen IV shows stabilization via a novel type of covalent Met-Lys cross-link.</Title>
-<Xref>DOI:10.1073/pnas.062183499</Xref>
-<Xref>PMID:12011424</Xref>
-<Note>X-ray diffraction, 1.9 angstroms; the cross-link is detected and postulated to be a thioether</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Than, M.E.</Author>
-<Author>Henrich, S.</Author>
-<Author>Huber, R.</Author>
-<Author>Ries, A.</Author>
-<Author>Mann, K.</Author>
-<Author>Kuhn, K.</Author>
-<Author>Timpl, R.</Author>
-<Author>Bourenkov, G.P.</Author>
-<Author>Bartunik, H.D.</Author>
-<Author>Bode, W.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, April 2002</Citation>
-<Description>The 1.9-a crystal structure of the noncollagenous (NC1) domain of human placenta collagen IV shows stabilization via a novel type of covalent Met-Lys cross-link.</Description>
-<Xref>PDB:1LI1</Xref>
-<Note>X-ray diffraction, 1.9 angstroms; although the cross-link is discussed as a thioether in the paper, it is not modeled in the PDB entry</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Vanacore, R.M.</Author>
-<Author>Friedman, D.B.</Author>
-<Author>Ham, A.J.</Author>
-<Author>Sundaramoorthy, M.</Author>
-<Author>Hudson, B.G.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 280, 29300-29310, 2005</Citation>
-<Title>Identification of S-hydroxylysyl-methionine as the covalent cross-link of the noncollagenous (NC1) hexamer of the alpha1alpha1alpha2 collagen IV network: a role for the post-translational modification of lysine 211 to hydroxylysine 211 in hexamer assembly.</Title>
-<Xref>DOI:10.1074/jbc.M502752200</Xref>
-<Xref>PMID:15951440</Xref>
-<Note>mass spectrometric detection and linkage analysis; the linkage is reduced by dithiothreitol, but the proposed link is a thioether</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Vanacore, R.</Author>
-<Author>Ham, A.J.</Author>
-<Author>Voehler, M.</Author>
-<Author>Sanders, C.R.</Author>
-<Author>Conrads, T.P.</Author>
-<Author>Veenstra, T.D.</Author>
-<Author>Sharpless, K.B.</Author>
-<Author>Dawson, P.E.</Author>
-<Author>Hudson, B.G.</Author>
-</Authors>
-<Citation>Science 325, 1230-1234, 2009</Citation>
-<Title>A sulfilimine bond identified in collagen IV.</Title>
-<Xref>DOI:10.1126/science.1176811</Xref>
-<Xref>PMID:19729652</Xref>
-<Note>mass spectrometric, (1)H-NMR, and (13)C-NMR identification; the proposed link is a sulfanylidene amine (-S=N-), referred to by the authors and Chemical Abstracts as a sulfilimine, and by IUPAC as a sulfimide</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ončák, M.</Author>
-<Author>Berka, K.</Author>
-<Author>Slavíček, P.</Author>
-</Authors>
-<Citation>Chemphyschem 12, 3449-3457, 2011</Citation>
-<Title>Novel covalent bond in proteins: calculations on model systems question the bond stability.</Title>
-<Xref>DOI:10.1002/cphc.201100664</Xref>
-<Xref>PMID:22144375</Xref>
-<Note>quantum mechanical molecular modeling</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bhave, G.</Author>
-<Author>Cummings, C.F.</Author>
-<Author>Vanacore, R.M.</Author>
-<Author>Kumagai-Cresse, C.</Author>
-<Author>Ero-Tolliver, I.A.</Author>
-<Author>Rafi, M.</Author>
-<Author>Kang, J.S.</Author>
-<Author>Pedchenko, V.</Author>
-<Author>Fessler, L.I.</Author>
-<Author>Fessler, J.H.</Author>
-<Author>Hudson, B.G.</Author>
-</Authors>
-<Citation>Nat. Chem. Biol. 8, 784-790, 2012</Citation>
-<Title>Peroxidasin forms sulfilimine chemical bonds using hypohalous acids in tissue genesis.</Title>
-<Xref>DOI:10.1038/nchembio.1038</Xref>
-<Xref>PMID:22842973</Xref>
-<Note>bromine oxidized to hypobromous acid by peroxidasin in basement membranes generates methionine bromosulfoniun that spontaneously reacts with lysine to form sulfilimine cross-link</Note>
-</ReferenceBlock>
-<Comment>The process for formation of the sulfanylimine bond has not been determined. It might involve the initial formation of methionine sulfoxide.</Comment>
-<Comment>The lysine involved in this cross-link in collagen IV is usually hydroxylated, but it is not subsequently glycosylated.</Comment>
-<SequenceCode>
-<SequenceSpec>K, M</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Condition>incidental to RESID:AA0028</Condition>
-<Xref>PSI-MOD:01602</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="crosslnk__s-lysyl-methionine sulfilimine (lys-met) (interchain with M-__k">CROSSLNK S-Lysyl-methionine sulfilimine (Lys-Met) (interchain with M-...)</Feature>
-<Feature type="UniProt" key="crosslnk__s-lysyl-methionine sulfilimine (met-lys) (interchain with K-__m">CROSSLNK S-Lysyl-methionine sulfilimine (Met-Lys) (interchain with K-...)</Feature>
-</Features>
-<Image src="/images/AA0501.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0501.PDB" />
-</Entry>
-<Entry id="AA0502">
-<Header>
-<Code>AA0502</Code>
-<Dates>
-<CreationDate>20-Nov-2009</CreationDate>
-<StrucRevDate>20-Nov-2009</StrucRevDate>
-<TextChngDate>13-Sep-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>5-glutamyl 2-aminoadipic acid</Name>
-<AlternateName>N2-(gamma-glutamyl)-2-aminoadipic acid</AlternateName>
-<AlternateName>N2-(isoglutamyl)-2-aminoadipic acid</AlternateName>
-<SystematicName>(2S)-2-([(4S)-4-amino-4-carboxybutanoyl]amino)hexanedioic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 11 H 16 N 2 O 6</Formula>
-<Weight type="chemical">272.26</Weight>
-<Weight type="physical">272.100836</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0006">
-<Formula>C 6 H 9 N 1 O 3</Formula>
-<Weight type="chemical">143.14</Weight>
-<Weight type="physical">143.058243</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Horie, A.</Author>
-<Author>Tomita, T.</Author>
-<Author>Saiki, A.</Author>
-<Author>Kono, H.</Author>
-<Author>Taka, H.</Author>
-<Author>Mineki, R.</Author>
-<Author>Fujimura, T.</Author>
-<Author>Nishiyama, C.</Author>
-<Author>Kuzuyama, T.</Author>
-<Author>Nishiyama, M.</Author>
-</Authors>
-<Citation>Nature Chem. Biol. 5, 673-679, 2009</Citation>
-<Title>Discovery of proteinaceous N-modification in lysine biosynthesis of Thermus thermophilus.</Title>
-<Xref>DOI:10.1038/nchembio.198</Xref>
-<Xref>PMID:19620981</Xref>
-<Note>mass spectrometric detection and linkage analysis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ouchi, T.</Author>
-<Author>Tomita, T.</Author>
-<Author>Horie, A.</Author>
-<Author>Yoshida, A.</Author>
-<Author>Takahashi, K.</Author>
-<Author>Nishida, H.</Author>
-<Author>Lassak, K.</Author>
-<Author>Taka, H.</Author>
-<Author>Mineki, R.</Author>
-<Author>Fujimura, T.</Author>
-<Author>Kosono, S.</Author>
-<Author>Nishiyama, C.</Author>
-<Author>Masui, R.</Author>
-<Author>Kuramitsu, S.</Author>
-<Author>Albers, S.V.</Author>
-<Author>Kuzuyama, T.</Author>
-<Author>Nishiyama, M.</Author>
-</Authors>
-<Citation>Nature Chem. Biol. 9, 277-283, 2013</Citation>
-<Title>Lysine and arginine biosyntheses mediated by a common carrier protein in Sulfolobus.</Title>
-<Xref>DOI:10.1038/nchembio.1200</Xref>
-<Xref>PMID:23434852</Xref>
-<Note>biosynthesis; mass spectrometric detection</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>alpha-aminoadipate--LysW ligase, LysX (EC 6.3.2.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>E</SequenceSpec>
-<Xref>PSI-MOD:01605</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="mod_res__5-glutamyl 2-aminoadipic acid__e">MOD_RES 5-glutamyl 2-aminoadipic acid</Feature>
-</Features>
-<Image src="/images/AA0502.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0502.PDB" />
-</Entry>
-<Entry id="AA0503">
-<Header>
-<Code>AA0503</Code>
-<Dates>
-<CreationDate>20-Nov-2009</CreationDate>
-<StrucRevDate>20-Nov-2009</StrucRevDate>
-<TextChngDate>13-Sep-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>5-glutamyl 2-aminoadipic 6-phosphoric anhydride</Name>
-<SystematicName>(2S)-2-([(4S)-4-amino-4-carboxybutanoyl]amino)-6-oxo-6-(phosphonooxy)hexanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 11 H 17 N 2 O 9 P 1</Formula>
-<Weight type="chemical">352.24</Weight>
-<Weight type="physical">352.067167</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0006">
-<Formula>C 6 H 10 N 1 O 6 P 1</Formula>
-<Weight type="chemical">223.12</Weight>
-<Weight type="physical">223.024574</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Horie, A.</Author>
-<Author>Tomita, T.</Author>
-<Author>Saiki, A.</Author>
-<Author>Kono, H.</Author>
-<Author>Taka, H.</Author>
-<Author>Mineki, R.</Author>
-<Author>Fujimura, T.</Author>
-<Author>Nishiyama, C.</Author>
-<Author>Kuzuyama, T.</Author>
-<Author>Nishiyama, M.</Author>
-</Authors>
-<Citation>Nature Chem. Biol. 5, 673-679, 2009</Citation>
-<Title>Discovery of proteinaceous N-modification in lysine biosynthesis of Thermus thermophilus.</Title>
-<Xref>DOI:10.1038/nchembio.198</Xref>
-<Xref>PMID:19620981</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ouchi, T.</Author>
-<Author>Tomita, T.</Author>
-<Author>Horie, A.</Author>
-<Author>Yoshida, A.</Author>
-<Author>Takahashi, K.</Author>
-<Author>Nishida, H.</Author>
-<Author>Lassak, K.</Author>
-<Author>Taka, H.</Author>
-<Author>Mineki, R.</Author>
-<Author>Fujimura, T.</Author>
-<Author>Kosono, S.</Author>
-<Author>Nishiyama, C.</Author>
-<Author>Masui, R.</Author>
-<Author>Kuramitsu, S.</Author>
-<Author>Albers, S.V.</Author>
-<Author>Kuzuyama, T.</Author>
-<Author>Nishiyama, M.</Author>
-</Authors>
-<Citation>Nature Chem. Biol. 9, 277-283, 2013</Citation>
-<Title>Lysine and arginine biosyntheses mediated by a common carrier protein in Sulfolobus.</Title>
-<Xref>DOI:10.1038/nchembio.1200</Xref>
-<Xref>PMID:23434852</Xref>
-<Note>biosynthesis; chemical detection using hydroxyl amine; mass spectrometric detection</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>LysW-L-glutamate/LysW-L-2-aminoadipate kinase, LysZ (EC 2.7.2.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>E</SequenceSpec>
-<Xref>PSI-MOD:01606</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0503.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0503.PDB" />
-</Entry>
-<Entry id="AA0504">
-<Header>
-<Code>AA0504</Code>
-<Dates>
-<CreationDate>20-Nov-2009</CreationDate>
-<StrucRevDate>20-Nov-2009</StrucRevDate>
-<TextChngDate>20-Nov-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>5-glutamyl allysine</Name>
-<AlternateName>2-(5-glutamyl)amino-6-oxohexanoic acid</AlternateName>
-<AlternateName>alpha-(gamma-glutamyl)allysine</AlternateName>
-<AlternateName>N2-(gamma-glutamyl)allysine</AlternateName>
-<AlternateName>N2-(isoglutamyl)allysine</AlternateName>
-<SystematicName>(2S)-2-([(4S)-4-amino-4-carboxybutanoyl]amino)-6-oxohexanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 11 H 16 N 2 O 5</Formula>
-<Weight type="chemical">256.26</Weight>
-<Weight type="physical">256.105922</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0006">
-<Formula>C 6 H 9 N 1 O 2</Formula>
-<Weight type="chemical">127.14</Weight>
-<Weight type="physical">127.063329</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Horie, A.</Author>
-<Author>Tomita, T.</Author>
-<Author>Saiki, A.</Author>
-<Author>Kono, H.</Author>
-<Author>Taka, H.</Author>
-<Author>Mineki, R.</Author>
-<Author>Fujimura, T.</Author>
-<Author>Nishiyama, C.</Author>
-<Author>Kuzuyama, T.</Author>
-<Author>Nishiyama, M.</Author>
-</Authors>
-<Citation>Nature Chem. Biol. 5, 673-679, 2009</Citation>
-<Title>Discovery of proteinaceous N-modification in lysine biosynthesis of Thermus thermophilus.</Title>
-<Xref>DOI:10.1038/nchembio.198</Xref>
-<Xref>PMID:19620981</Xref>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>E</SequenceSpec>
-<Xref>PSI-MOD:01607</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0504.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0504.PDB" />
-</Entry>
-<Entry id="AA0505">
-<Header>
-<Code>AA0505</Code>
-<Dates>
-<CreationDate>20-Nov-2009</CreationDate>
-<StrucRevDate>20-Nov-2009</StrucRevDate>
-<TextChngDate>20-Nov-2009</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N2-(L-isoglutamyl)-L-lysine</Name>
-<AlternateName>5-glutamyl N2-lysine</AlternateName>
-<AlternateName>alpha-(gamma-glutamyl)lysine</AlternateName>
-<AlternateName>gamma-glutamyl N2-lysine</AlternateName>
-<AlternateName>N2-(gamma-glutamyl)lysine</AlternateName>
-<SystematicName>(2S)-6-amino-2-([(4S)-4-amino-4-carboxybutanoyl]amino)hexanoic acid</SystematicName>
-<Xref>CAS:5978-23-4</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 11 H 19 N 3 O 4</Formula>
-<Weight type="chemical">257.29</Weight>
-<Weight type="physical">257.137556</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0006">
-<Formula>C 6 H 12 N 2 O 1</Formula>
-<Weight type="chemical">128.18</Weight>
-<Weight type="physical">128.094963</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Horie, A.</Author>
-<Author>Tomita, T.</Author>
-<Author>Saiki, A.</Author>
-<Author>Kono, H.</Author>
-<Author>Taka, H.</Author>
-<Author>Mineki, R.</Author>
-<Author>Fujimura, T.</Author>
-<Author>Nishiyama, C.</Author>
-<Author>Kuzuyama, T.</Author>
-<Author>Nishiyama, M.</Author>
-</Authors>
-<Citation>Nature Chem. Biol. 5, 673-679, 2009</Citation>
-<Title>Discovery of proteinaceous N-modification in lysine biosynthesis of Thermus thermophilus.</Title>
-<Xref>DOI:10.1038/nchembio.198</Xref>
-<Xref>PMID:19620981</Xref>
-<Note>mass spectrometric detection and linkage analysis</Note>
-</ReferenceBlock>
-<Comment>For the cross-linking of a peptidyl glutamine or glutamic acid by isopeptide bond through the gamma-carboxyl group to the N6-amino of a peptidyl lysine, see RESID:AA0124.</Comment>
-<SequenceCode>
-<SequenceSpec>E</SequenceSpec>
-<Xref>PSI-MOD:01608</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>isopeptide bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__5-glutamyl n2-lysine__e">MOD_RES 5-glutamyl N2-lysine</Feature>
-</Features>
-<Image src="/images/AA0505.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0505.PDB" />
-</Entry>
-<Entry id="AA0506">
-<Header>
-<Code>AA0506</Code>
-<Dates>
-<CreationDate>20-Nov-2009</CreationDate>
-<StrucRevDate>20-Nov-2009</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>7'-hydroxy-2'-alpha-mannosyl-L-tryptophan</Name>
-<SystematicName>(2S)-2-amino-3-[7-hydroxy-2-(alpha-D-mannopyranosyl)-1H-indol-3-yl]propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 17 H 20 N 2 O 7</Formula>
-<Weight type="chemical">364.35</Weight>
-<Weight type="physical">364.127051</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0018">
-<Formula>C 6 H 10 N 0 O 6</Formula>
-<Weight type="chemical">178.14</Weight>
-<Weight type="physical">178.047738</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Zhao, H.</Author>
-<Author>Sagert, J.</Author>
-<Author>Hwang, D.S.</Author>
-<Author>Waite, J.H.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 284, 23344-23352, 2009</Citation>
-<Title>Glycosylated hydroxytryptophan in a mussel adhesive protein from Perna viridis.</Title>
-<Xref>DOI:10.1074/jbc.M109.022517</Xref>
-<Xref>PMID:19584055</Xref>
-<Note>mass spectrometric detection, spectrographic and chemical characterization</Note>
-</ReferenceBlock>
-<Comment>The 7'-hydroxylation of tryptophan apparently makes it susceptible to oxidation and cross-linking, however these secondary products have not been characterized.</Comment>
-<SequenceCode>
-<SequenceSpec>W</SequenceSpec>
-<Condition>secondary to RESID:AA0217</Condition>
-<Condition>secondary to RESID:AA0521</Condition>
-<Xref>PSI-MOD:01609</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__c-linked (man) hydroxytryptophan__w">CARBOHYD C-linked (Man) hydroxytryptophan</Feature>
-</Features>
-<Image src="/images/AA0506.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0506.PDB" />
-</Entry>
-<Entry id="AA0507">
-<Header>
-<Code>AA0507</Code>
-<Dates>
-<CreationDate>31-Dec-2009</CreationDate>
-<StrucRevDate>31-Dec-2009</StrucRevDate>
-<TextChngDate>30-Jun-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-threonine methyl ester</Name>
-<AlternateName>methyl L-threoninate</AlternateName>
-<SystematicName>methyl (2S,3R)-2-amino-3-hydroxybutanoate</SystematicName>
-<Xref>CAS:3373-59-9</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 10 N 1 O 3</Formula>
-<Weight type="chemical">132.14</Weight>
-<Weight type="physical">132.066068</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0017">
-<Formula>C 1 H 2 N 0 O 0</Formula>
-<Weight type="chemical">14.03</Weight>
-<Weight type="physical">14.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mukai, A.</Author>
-<Author>Fukai, T.</Author>
-<Author>Hoshino, Y.</Author>
-<Author>Yazawa, K.</Author>
-<Author>Harada, K.-I.</Author>
-<Author>Mikami, Y.</Author>
-</Authors>
-<Citation>J. Antibiot. 62, 613-619, 2009</Citation>
-<Title>Nocardithiocin, a novel thiopeptide antibiotic, produced by pathogenic Nocardia pseudobrasiliensis IFM 0757.</Title>
-<Xref>DOI:10.1038/ja.2009.90</Xref>
-<Xref>PMID:19745839</Xref>
-<Note>the initials of K.-I. Harada in the PubMed citation are corrected</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>T</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Condition>incidental to RESID:AA0182</Condition>
-<Xref>GO:0044608</Xref>
-<Xref>PSI-MOD:01610</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>methylated carboxyl end</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0507.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0507.PDB" />
-</Entry>
-<Entry id="AA0508">
-<Header>
-<Code>AA0508</Code>
-<Dates>
-<CreationDate>31-Dec-2009</CreationDate>
-<StrucRevDate>31-Dec-2009</StrucRevDate>
-<TextChngDate>30-Apr-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>6-(S-L-cysteinyl)-8alpha-(N3'-L-histidino)-FMN</Name>
-<AlternateName>6-(S-cysteinyl)-8alpha-(N(delta)-histidyl)-FMN</AlternateName>
-<AlternateName>6-(S-cysteinyl)-8alpha-(N(pi)-histidyl)-FMN</AlternateName>
-<AlternateName>6-(S-cysteinyl)-8alpha-(N3'-histidyl)-FMN</AlternateName>
-<AlternateName>6-(S-cysteinyl)-8alpha-(pros-histidyl)-FMN</AlternateName>
-<SystematicName>6-((R)-2-amino-2-carboxyethyl)sulfanyl-8alpha-[4-((S)-2-amino-2-carboxyethyl)imidazol-3-yl]-riboflavin 5'-trihydrogen phosphate</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 26 H 29 N 8 O 11 P 1 S 1</Formula>
-<Weight type="chemical">692.60</Weight>
-<Weight type="physical">692.141411</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0009">
-<Formula>C 17 H 17 N 4 O 9 P 1 S 0</Formula>
-<Weight type="chemical">452.32</Weight>
-<Weight type="physical">452.073315</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Li, Y.S.</Author>
-<Author>Ho, J.Y.</Author>
-<Author>Huang, C.C.</Author>
-<Author>Lyu, S.Y.</Author>
-<Author>Lee, C.Y.</Author>
-<Author>Huang, Y.T.</Author>
-<Author>Wu, C.J.</Author>
-<Author>Chan, H.C.</Author>
-<Author>Huang, C.J.</Author>
-<Author>Hsu, N.S.</Author>
-<Author>Tsai, M.D.</Author>
-<Author>Li, T.L.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 129, 13384-13385, 2007</Citation>
-<Title>A unique flavin mononucleotide-linked primary alcohol oxidase for glycopeptide A40926 maturation.</Title>
-<Xref>DOI:10.1021/ja075748x</Xref>
-<Xref>PMID:17935335</Xref>
-<Note>mass spectrometric identification, directed mutation analysis</Note>
-</ReferenceBlock>
-<Comment>The keyword "phosphoprotein" is not used with flavin modifications linked through the flavin.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C, H</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:01611</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>*phosphoprotein</Keyword>
-<Keyword>flavoprotein</Keyword>
-<Keyword>FMN</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="binding__fmn (covalent; via 2 links, pros nitrogen)__h">BINDING FMN (covalent; via 2 links, pros nitrogen)</Feature>
-<Feature type="UniProt" key="binding__fmn (covalent; via 2 links)__c">BINDING FMN (covalent; via 2 links)</Feature>
-</Features>
-<Image src="/images/AA0508.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0508.PDB" />
-</Entry>
-<Entry id="AA0509">
-<Header>
-<Code>AA0509</Code>
-<Dates>
-<CreationDate>31-Dec-2009</CreationDate>
-<StrucRevDate>31-Dec-2009</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>3'-iodo-L-tyrosine</Name>
-<AlternateName>3-iodo-L-tyrosine</AlternateName>
-<AlternateName>3-iodotyrosine</AlternateName>
-<AlternateName>4-hydroxy-3-iodo-phenylalanine</AlternateName>
-<AlternateName>MIT</AlternateName>
-<SystematicName>(2S)-2-amino-3-(4-hydroxy-3-iodophenyl)propanoic acid</SystematicName>
-<Xref>CAS:70-78-0</Xref>
-<Xref>ChEBI:90870</Xref>
-<Xref>PDBHET:IYR</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 8 I 1 N 1 O 2</Formula>
-<Weight type="chemical">289.07</Weight>
-<Weight type="physical">288.959976</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0019">
-<Formula>C 0 H -1 I 1 N 0 O 0</Formula>
-<Weight type="chemical">125.90</Weight>
-<Weight type="physical">125.896648</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gentile, F.</Author>
-<Author>Ferranti, P.</Author>
-<Author>Mamone, G.</Author>
-<Author>Malorni, A.</Author>
-<Author>Salvatore, G.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 272, 639-646, 1997</Citation>
-<Title>Identification of hormonogenic tyrosines in fragment 1218-1591 of bovine thyroglobulin by mass spectrometry. Hormonogenic acceptor TYR-12donor TYR-1375.</Title>
-<Xref>DOI:10.1074/jbc.272.1.639</Xref>
-<Xref>PMID:8995307</Xref>
-<Note>mass spectrometric detection</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>Y</SequenceSpec>
-<Xref>PSI-MOD:01612</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>iodine</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__iodotyrosine__y">MOD_RES Iodotyrosine</Feature>
-</Features>
-<Image src="/images/AA0509.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0509.PDB" />
-</Entry>
-<Entry id="AA0510">
-<Header>
-<Code>AA0510</Code>
-<Dates>
-<CreationDate>31-Dec-2009</CreationDate>
-<StrucRevDate>31-Dec-2009</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>3',5'-diiodo-L-tyrosine</Name>
-<AlternateName>3,5-diiodo-L-tyrosine</AlternateName>
-<AlternateName>3,5-diiodotyrosine</AlternateName>
-<AlternateName>DIT</AlternateName>
-<AlternateName>iodogorgoic acid</AlternateName>
-<SystematicName>(2S)-2-amino-3-(4-hydroxy-3,5-diiodophenyl)propanoic acid</SystematicName>
-<Xref>CAS:300-39-0</Xref>
-<Xref>ChEBI:90871</Xref>
-<Xref>PDBHET:TYI</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 7 I 2 N 1 O 2</Formula>
-<Weight type="chemical">414.97</Weight>
-<Weight type="physical">414.856624</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0019">
-<Formula>C 0 H -2 I 2 N 0 O 0</Formula>
-<Weight type="chemical">251.79</Weight>
-<Weight type="physical">251.793295</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gentile, F.</Author>
-<Author>Ferranti, P.</Author>
-<Author>Mamone, G.</Author>
-<Author>Malorni, A.</Author>
-<Author>Salvatore, G.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 272, 639-646, 1997</Citation>
-<Title>Identification of hormonogenic tyrosines in fragment 1218-1591 of bovine thyroglobulin by mass spectrometry. Hormonogenic acceptor TYR-12donor TYR-1375.</Title>
-<Xref>DOI:10.1074/jbc.272.1.639</Xref>
-<Xref>PMID:8995307</Xref>
-<Note>mass spectrometric detection</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>Y</SequenceSpec>
-<Xref>PSI-MOD:01613</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>iodine</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__diiodotyrosine__y">MOD_RES Diiodotyrosine</Feature>
-</Features>
-<Image src="/images/AA0510.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0510.PDB" />
-</Entry>
-<Entry id="AA0511">
-<Header>
-<Code>AA0511</Code>
-<Dates>
-<CreationDate>31-Dec-2009</CreationDate>
-<StrucRevDate>31-Dec-2009</StrucRevDate>
-<TextChngDate>20-May-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>glycyl phospho-5'-adenosine</Name>
-<AlternateName>(2-aminoacetyl)oxy-([(2R,3R,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxy-oxolan-2-yl]methoxy)phosphinic acid</AlternateName>
-<AlternateName>([(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxy-oxolan-2-yl]methoxy-hydroxy-phosphoryl)-2-aminoethanoate</AlternateName>
-<AlternateName>5'-adenylic-glyinate</AlternateName>
-<AlternateName>glycine monoanhydride with 5'-adenylic acid</AlternateName>
-<AlternateName>glycyl 5'-adenylate</AlternateName>
-<AlternateName>glycyl adenosine-5'-phosphate</AlternateName>
-<AlternateName>glycyladenylate</AlternateName>
-<SystematicName>aminoacetyl [5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methyl hydrogen phosphate</SystematicName>
-<Xref>CAS:35985-26-3</Xref>
-<Xref>PDBHET:AMP</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 12 H 16 N 6 O 8 P 1</Formula>
-<Weight type="chemical">403.27</Weight>
-<Weight type="physical">403.076723</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0008">
-<Formula>C 10 H 12 N 5 O 6 P 1</Formula>
-<Weight type="chemical">329.21</Weight>
-<Weight type="physical">329.052520</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Taylor, S.V.</Author>
-<Author>Kelleher, N.L.</Author>
-<Author>Kinsland, C.</Author>
-<Author>Chiu, H.J.</Author>
-<Author>Costello, C.A.</Author>
-<Author>Backstrom, A.D.</Author>
-<Author>McLafferty, F.W.</Author>
-<Author>Begley, T.P.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 273, 16555-16560, 1998</Citation>
-<Title>Thiamin biosynthesis in Escherichia coli. Identification of ThiS thiocarboxylate as the immediate sulfur donor in the thiazole formation.</Title>
-<Xref>DOI:10.1074/jbc.273.26.16555</Xref>
-<Xref>PMID:9632726</Xref>
-<Note>mass spectrometric identification; the capitalization of ThiS in the PubMed citation is corrected</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lake, M.W.</Author>
-<Author>Wuebbens, M.M.</Author>
-<Author>Rajagopalan, K.V.</Author>
-<Author>Schindelin, H.</Author>
-</Authors>
-<Citation>Nature 414, 325-329, 2001</Citation>
-<Title>Mechanism of ubiquitin activation revealed by the structure of a bacterial MoeB-MoaD complex.</Title>
-<Xref>DOI:10.1038/35104586</Xref>
-<Xref>PMID:11713534</Xref>
-<Note>X-ray diffraction, 2.10 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lake, M.W.</Author>
-<Author>Wuebbens, M.M.</Author>
-<Author>Rajagopalan, K.V.</Author>
-<Author>Schindelin, H.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, September 2001</Citation>
-<Description>Structure of the covalent acyl-adenylate form of the MoeB-MoaD protein complex.</Description>
-<Xref>PDB:1JWB</Xref>
-<Note>X-ray diffraction, 2.50 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lehmann, C.</Author>
-<Author>Begley, T.P.</Author>
-<Author>Ealick, S.E.</Author>
-</Authors>
-<Citation>Biochemistry 45, 11-19, 2006</Citation>
-<Title>Structure of the Escherichia coli ThiS-ThiF complex, a key component of the sulfur transfer system in thiamin biosynthesis.</Title>
-<Xref>DOI:10.1021/bi051502y</Xref>
-<Xref>PMID:16388576</Xref>
-<Note>X-ray diffraction, 1.98 angstroms, of the ThiS-ThiF complex with discussion of models of the proposed intermediates</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>G</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>PSI-MOD:01614</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__glycyl adenylate__g">MOD_RES Glycyl adenylate</Feature>
-</Features>
-<Image src="/images/AA0511.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0511.PDB" />
-</Entry>
-<Entry id="AA0512">
-<Header>
-<Code>AA0512</Code>
-<Dates>
-<CreationDate>31-Dec-2009</CreationDate>
-<StrucRevDate>31-Dec-2009</StrucRevDate>
-<TextChngDate>25-Feb-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>glycyl cysteine dithioester</Name>
-<AlternateName>2-(glycyldithio)alanine</AlternateName>
-<AlternateName>S-glycyl cysteine persulfide</AlternateName>
-<AlternateName>S-glycyl thiocysteine</AlternateName>
-<AlternateName>thioglycine cysteine disulfide</AlternateName>
-<SystematicName>(2R)-2-amino-3-[(aminoacetyl)disulfanyl]propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 7 N 2 O 2 S 2</Formula>
-<Weight type="chemical">191.24</Weight>
-<Weight type="physical">190.994894</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0008">
-<Formula>C 0 H -2 N 0 O -1 S 1</Formula>
-<Weight type="chemical">14.05</Weight>
-<Weight type="physical">13.961506</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Xi, J.</Author>
-<Author>Ge, Y.</Author>
-<Author>Kinsland, C.</Author>
-<Author>McLafferty, F.W.</Author>
-<Author>Begley, T.P.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 98, 8513-8518, 2001</Citation>
-<Title>Biosynthesis of the thiazole moiety of thiamin in Escherichia coli: identification of an acyldisulfide-linked protein--protein conjugate that is functionally analogous to the ubiquitin/E1 complex.</Title>
-<Xref>DOI:10.1073/pnas.141226698</Xref>
-<Xref>PMID:11438688</Xref>
-<Note>mass spectrometric evidence</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lehmann, C.</Author>
-<Author>Begley, T.P.</Author>
-<Author>Ealick, S.E.</Author>
-</Authors>
-<Citation>Biochemistry 45, 11-19, 2006</Citation>
-<Title>Structure of the Escherichia coli ThiS-ThiF complex, a key component of the sulfur transfer system in thiamin biosynthesis.</Title>
-<Xref>DOI:10.1021/bi051502y</Xref>
-<Xref>PMID:16388576</Xref>
-<Note>X-ray diffraction, 1.98 angstroms, of the ThiS-ThiF complex with discussion of models of the proposed intermediates</Note>
-</ReferenceBlock>
-<Comment>These are highly reactive dithioester cross-links formed between internal cysteine residues of ThiF and the carboxyl end of ThiS and other similar proteins.</Comment>
-<SequenceCode>
-<SequenceSpec>C, G</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:01615</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>thioester bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__glycyl cysteine dithioester (gly-cys) (interchain with c-__g">CROSSLNK Glycyl cysteine dithioester (Gly-Cys) (interchain with C-...)</Feature>
-<Feature type="UniProt" key="crosslnk__glycyl cysteine dithioester (cys-gly) (interchain with g-cter__c">CROSSLNK Glycyl cysteine dithioester (Cys-Gly) (interchain with G-Cter ...)</Feature>
-</Features>
-<Image src="/images/AA0512.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0512.PDB" />
-</Entry>
-<Entry id="AA0513">
-<Header>
-<Code>AA0513</Code>
-<Dates>
-<CreationDate>29-Jan-2010</CreationDate>
-<StrucRevDate>29-Jan-2010</StrucRevDate>
-<TextChngDate>29-Jan-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>trithiocystine</Name>
-<AlternateName>3,3'-pentathiobisalanine</AlternateName>
-<AlternateName>bis(2-amino-2-carboxyethyl)pentasulfide</AlternateName>
-<SystematicName>(2R,2'R)-3,3'-pentasulfane-1,5-diylbis(2-aminopropanoic acid)</SystematicName>
-<Xref>PDBHET:S3H</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 8 N 2 O 2 S 5</Formula>
-<Weight type="chemical">300.44</Weight>
-<Weight type="physical">299.918933</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005">
-<Formula>C 0 H -2 N 0 O 0 S 3</Formula>
-<Weight type="chemical">94.16</Weight>
-<Weight type="physical">93.900563</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Brito, J.A.</Author>
-<Author>Sousa, F.L.</Author>
-<Author>Stelter, M.</Author>
-<Author>Bandeiras, T.M.</Author>
-<Author>Vonrhein, C.</Author>
-<Author>Teixeira, M.</Author>
-<Author>Pereira, M.M.</Author>
-<Author>Archer, M.</Author>
-</Authors>
-<Citation>Biochemistry 48, 5613-5622, 2009</Citation>
-<Title>Structural and functional insights into sulfide:quinone oxidoreductase.</Title>
-<Xref>DOI:10.1021/bi9003827</Xref>
-<Xref>PMID:19438211</Xref>
-<Note>X-ray diffraction, 2.57 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Brito, J.A.</Author>
-<Author>Sousa, F.L.</Author>
-<Author>Stelter, M.</Author>
-<Author>Bandeiras, T.M.</Author>
-<Author>Vonrhein, C.</Author>
-<Author>Teixeira, M.</Author>
-<Author>Pereira, M.M.</Author>
-<Author>Archer, M.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, April 2009</Citation>
-<Description>The first X-ray structure of a sulfide:quinone oxidoreductase: insights into sulfide oxidation mechanism.</Description>
-<Xref>PDB:3H8L</Xref>
-<Note>X-ray diffraction, 2.57 angstroms</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>C, C</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:01616</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0513.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0513.PDB" />
-</Entry>
-<Entry id="AA0514">
-<Header>
-<Code>AA0514</Code>
-<Dates>
-<CreationDate>29-Jan-2010</CreationDate>
-<StrucRevDate>29-Jan-2010</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-(6-phosphomannosyl)-L-threonine</Name>
-<AlternateName>O3-(6-phosphomannosyl)threonine</AlternateName>
-<SystematicName>(2S,3R)-2-amino-3-[6-phosphonooxy-alpha-D-mannopyranosyloxy]butanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 10 H 18 N 1 O 10 P 1 +</Formula>
-<Weight type="chemical">343.22 +</Weight>
-<Weight type="physical">343.066832 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0017">
-<Formula>C 6 H 11 N 0 O 8 P 1 +</Formula>
-<Weight type="chemical">242.12 +</Weight>
-<Weight type="physical">242.019154 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yoshida-Moriguchi, T.</Author>
-<Author>Yu, L.</Author>
-<Author>Stalnaker, S.H.</Author>
-<Author>Davis, S.</Author>
-<Author>Kunz, S.</Author>
-<Author>Madson, M.</Author>
-<Author>Oldstone, M.B.</Author>
-<Author>Schachter, H.</Author>
-<Author>Wells, L.</Author>
-<Author>Campbell, K.P.</Author>
-</Authors>
-<Citation>Science 327, 88-92, 2010</Citation>
-<Title>O-mannosyl phosphorylation of alpha-dystroglycan is required for laminin binding.</Title>
-<Xref>DOI:10.1126/science.1180512</Xref>
-<Xref>PMID:20044576</Xref>
-<Note>mass spectrometric, (1)H-NMR, and (13)C-NMR identification; the structure was determined to be O3-[N-acetylgalactosaminyl-beta-1,3-N-acetylglucosaminyl-beta-1,4-(6-phospho-)mannosyl]threonine</Note>
-</ReferenceBlock>
-<Comment>The alpha anomeric form is shown.</Comment>
-<Comment>See also RESID:AA0155, RESID:AA0247, RESID:AA0399, RESID:AA0401, RESID:AA0403, and RESID:AA0405 for other O-glycosylated threonines.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>protein O-mannosyl transferase (EC 2.4.1.109)</EnzymeName>
-<EnzymeName>protein O-mannose beta-1,4-N-acetylglucosaminyltransferase (EC 2.4.1.-)</EnzymeName>
-<EnzymeName>protein O-(N-acetylglucosaminyl-beta-1,4)-mannose beta-1,4-N-acetylgalactosaminyltransferase (EC 2.4.1.-)</EnzymeName>
-<EnzymeName>protein O-mannose 6-phosphotransferase (EC 2.7.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>T</SequenceSpec>
-<Xref>PSI-MOD:01617</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__o-linked (man6p...) threonine__t">CARBOHYD O-linked (Man6P...) threonine</Feature>
-</Features>
-<Image src="/images/AA0514.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0514.PDB" />
-</Entry>
-<Entry id="AA0515">
-<Header>
-<Code>AA0515</Code>
-<Dates>
-<CreationDate>29-Jan-2010</CreationDate>
-<StrucRevDate>29-Jan-2010</StrucRevDate>
-<TextChngDate>30-Jun-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-alanyl-L-isoaspartyl cyclopeptide</Name>
-<AlternateName>1,4.2-anhydro(L-alanyl-L-aspartic acid)</AlternateName>
-<SystematicName>(2S,5S)-2-methyl-3,7-dioxo-1,4-diazepane-5-carboxylic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 9 N 2 O 3</Formula>
-<Weight type="chemical">169.16</Weight>
-<Weight type="physical">169.061317</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0001 AA0003">
-<Formula>C 0 H -3 N -1 O 0</Formula>
-<Weight type="chemical">-17.03</Weight>
-<Weight type="physical">-17.026549</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lura, R.</Author>
-<Author>Schirch, V.</Author>
-</Authors>
-<Citation>Biochemistry 27, 7671-7677, 1988</Citation>
-<Title>Role of peptide conformation in the rate and mechanism of deamidation of asparaginyl residues.</Title>
-<Xref>DOI:10.1021/bi00420a015</Xref>
-<Xref>PMID:3207697</Xref>
-<Note>chemical and (1)H-NMR evidence for formation of a valyl-isoaspartyl cyclopeptide from a synthetic tetrapeptide valyl-asparaginyl-glycyl-alanine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kita, M.</Author>
-<Author>Black, D.S.</Author>
-<Author>Ohno, O.</Author>
-<Author>Yamada, K.</Author>
-<Author>Kigoshi, H.</Author>
-<Author>Uemura, D.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 131, 18038-18039, 2009</Citation>
-<Title>Duck-billed platypus venom peptides induce Ca2+ influx in neuroblastoma cells.</Title>
-<Xref>DOI:10.1021/ja908148z</Xref>
-<Xref>PMID:19928958</Xref>
-<Note>mass spectrometric detection of cyclic deamidation; an alternate cyclization is not ruled out</Note>
-</ReferenceBlock>
-<Comment>This is a proposed cyclization between asparagine and the free amino group of the preceding amino acid in a peptide. It is more probable that asparagine cyclizes with the amino group of the following glycine, see RESID:AA0441.</Comment>
-<SequenceCode>
-<SequenceSpec>A, N</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Condition>cross-link 1</Condition>
-<Xref>PSI-MOD:01618</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Features>
-<Feature type="UniProt" key="crosslnk__alanine isoaspartyl cyclopeptide (ala-asn)__a__n">CROSSLNK Alanine isoaspartyl cyclopeptide (Ala-Asn)</Feature>
-</Features>
-<Image src="/images/AA0515.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0515.PDB" />
-</Entry>
-<Entry id="AA0516">
-<Header>
-<Code>AA0516</Code>
-<Dates>
-<CreationDate>26-Feb-2010</CreationDate>
-<StrucRevDate>26-Feb-2010</StrucRevDate>
-<TextChngDate>29-May-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-[(12R)-12-hydroxymyristoyl]-L-cysteine</Name>
-<AlternateName>N-[(12R)-12-hydroxytetradecanoyl]cysteine</AlternateName>
-<SystematicName>2-[(12R)-12-hydroxytetradecanoyl]amino-3-sulfanylpropanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 17 H 32 N 1 O 3 S 1</Formula>
-<Weight type="chemical">330.51</Weight>
-<Weight type="physical">330.210290</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 14 H 26 N 0 O 2 S 0</Formula>
-<Weight type="chemical">226.36</Weight>
-<Weight type="physical">226.193280</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Whitson, E.L.</Author>
-<Author>Ratnayake, A.S.</Author>
-<Author>Bugni, T.S.</Author>
-<Author>Harper, M.K.</Author>
-<Author>Ireland, C.M.</Author>
-</Authors>
-<Citation>J. Org. Chem. 74, 1156-1162, 2009</Citation>
-<Title>Isolation, structure elucidation, and synthesis of eudistomides A and B, lipopeptides from a Fijian ascidian Eudistoma sp.</Title>
-<Xref>DOI:10.1021/jo8022582</Xref>
-<Xref>PMID:19053188</Xref>
-<Note>mass spectrometric, (1)H-NMR, and (13)C-NMR identification; chemical synthesis</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>PSI-MOD:01690</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lipoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__n-[(12r)-12-hydroxymyristoyl]cysteine">LIPID N-[(12R)-12-hydroxymyristoyl]cysteine</Feature>
-</Features>
-<Image src="/images/AA0516.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0516.PDB" />
-</Entry>
-<Entry id="AA0517">
-<Header>
-<Code>AA0517</Code>
-<Dates>
-<CreationDate>26-Feb-2010</CreationDate>
-<StrucRevDate>26-Feb-2010</StrucRevDate>
-<TextChngDate>29-May-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-(12-ketomyristoyl)-L-cysteine</Name>
-<AlternateName>N-(12-oxotetradecanoyl)cysteine</AlternateName>
-<SystematicName>2-(12-oxotetradecanoyl)amino-3-sulfanylpropanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 17 H 30 N 1 O 3 S 1</Formula>
-<Weight type="chemical">328.49</Weight>
-<Weight type="physical">328.194640</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 14 H 24 N 0 O 2 S 0</Formula>
-<Weight type="chemical">224.34</Weight>
-<Weight type="physical">224.177630</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Whitson, E.L.</Author>
-<Author>Ratnayake, A.S.</Author>
-<Author>Bugni, T.S.</Author>
-<Author>Harper, M.K.</Author>
-<Author>Ireland, C.M.</Author>
-</Authors>
-<Citation>J. Org. Chem. 74, 1156-1162, 2009</Citation>
-<Title>Isolation, structure elucidation, and synthesis of eudistomides A and B, lipopeptides from a Fijian ascidian Eudistoma sp.</Title>
-<Xref>DOI:10.1021/jo8022582</Xref>
-<Xref>PMID:19053188</Xref>
-<Note>mass spectrometric, (1)H-NMR, and (13)C-NMR identification; chemical synthesis</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>PSI-MOD:01691</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lipoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__n-(12-oxomyristoyl)cysteine">LIPID N-(12-oxomyristoyl)cysteine</Feature>
-</Features>
-<Image src="/images/AA0517.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0517.PDB" />
-</Entry>
-<Entry id="AA0518">
-<Header>
-<Code>AA0518</Code>
-<Dates>
-<CreationDate>31-Mar-2010</CreationDate>
-<StrucRevDate>31-Mar-2010</StrucRevDate>
-<TextChngDate>29-Oct-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N5-(ADP-ribosyl)-L-glutamine</Name>
-<AlternateName>N5-alpha-D-ribofuranosyl-L-glutamine 5'->5'-ester with adenosine 5'-(trihydrogen diphosphate)</AlternateName>
-<AlternateName>N5-[alpha-D-ribofuranoside 5'->5'-ester with adenosine 5'-(trihydrogen diphosphate)]-L-glutamine</AlternateName>
-<SystematicName>(S)-2-amino-4-([adenosine 5'-(trihydrogen diphosphate) 5'->5'-ester with alpha-D-ribofuranosyl]amino)-5-oxopentanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 20 H 29 N 7 O 15 P 2</Formula>
-<Weight type="chemical">669.43</Weight>
-<Weight type="physical">669.119687</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0007">
-<Formula>C 15 H 21 N 5 O 13 P 2</Formula>
-<Weight type="chemical">541.30</Weight>
-<Weight type="physical">541.061109</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lang, A.E.</Author>
-<Author>Schmidt, G.</Author>
-<Author>Schlosser, A.</Author>
-<Author>Hey, T.D.</Author>
-<Author>Larrinua, I.M.</Author>
-<Author>Sheets, J.J.</Author>
-<Author>Mannherz, H.G.</Author>
-<Author>Aktories, K.</Author>
-</Authors>
-<Citation>Science 327, 1139-1142, 2010</Citation>
-<Title>Photorhabdus luminescens toxins ADP-ribosylate actin and RhoA to force actin clustering.</Title>
-<Xref>DOI:10.1126/science.1184557</Xref>
-<Xref>PMID:20185726</Xref>
-</ReferenceBlock>
-<Comment>It is not known whether Photorhabdus luminescens toxin catalyzes formation of the alpha or beta isomer. The alpha form is presented.</Comment>
-<Comment>The keyword "phosphoprotein" is not used with toxin modification.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>NAD(P)+--glutamine ADP-ribosyltransferase TccC5 (EC 2.4.2.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>Q</SequenceSpec>
-<Xref>PSI-MOD:01662</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>*phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0518.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0518.PDB" />
-</Entry>
-<Entry id="AA0519">
-<Header>
-<Code>AA0519</Code>
-<Dates>
-<CreationDate>31-Mar-2010</CreationDate>
-<StrucRevDate>31-Mar-2010</StrucRevDate>
-<TextChngDate>29-Oct-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-(ADP-ribosyl)-L-threonine</Name>
-<AlternateName>O3-(ADP-ribosyl)-L-threonine</AlternateName>
-<AlternateName>O3-alpha-D-ribofuranosyl-L-threonine 5'->5'-ester with adenosine 5'-(trihydrogen diphosphate)</AlternateName>
-<AlternateName>O3-[alpha-D-ribofuranoside 5'->5'-ester with adenosine 5'-(trihydrogen diphosphate)]-L-threonine</AlternateName>
-<SystematicName>(S)-2-amino-3-([adenosine 5'-(trihydrogen diphosphate) 5'->5'-ester with alpha-D-ribofuranosyl]oxy)-butanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 19 H 28 N 6 O 15 P 2</Formula>
-<Weight type="chemical">642.41</Weight>
-<Weight type="physical">642.108787</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0017">
-<Formula>C 15 H 21 N 5 O 13 P 2</Formula>
-<Weight type="chemical">541.30</Weight>
-<Weight type="physical">541.061109</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lang, A.E.</Author>
-<Author>Schmidt, G.</Author>
-<Author>Schlosser, A.</Author>
-<Author>Hey, T.D.</Author>
-<Author>Larrinua, I.M.</Author>
-<Author>Sheets, J.J.</Author>
-<Author>Mannherz, H.G.</Author>
-<Author>Aktories, K.</Author>
-</Authors>
-<Citation>Science 327, 1139-1142, 2010</Citation>
-<Title>Photorhabdus luminescens toxins ADP-ribosylate actin and RhoA to force actin clustering.</Title>
-<Xref>DOI:10.1126/science.1184557</Xref>
-<Xref>PMID:20185726</Xref>
-</ReferenceBlock>
-<Comment>It is not known whether Photorhabdus luminescens toxin catalyzes formation of the alpha or beta isomer. The alpha form is presented.</Comment>
-<Comment>The keyword "phosphoprotein" is not used with toxin modification.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>NAD(P)+--threonine ADP-ribosyltransferase TccC3 (EC 2.4.2.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>T</SequenceSpec>
-<Xref>PSI-MOD:01663</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>*phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0519.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0519.PDB" />
-</Entry>
-<Entry id="AA0520">
-<Header>
-<Code>AA0520</Code>
-<Dates>
-<CreationDate>31-Mar-2010</CreationDate>
-<StrucRevDate>31-Mar-2010</StrucRevDate>
-<TextChngDate>31-Mar-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>7'-hydroxy-L-tryptophan</Name>
-<AlternateName>7-hydroxy-L-tryptophan</AlternateName>
-<SystematicName>(2S)-2-amino-3-(7-hydroxy-1H-indol-3-yl)propanoic acid</SystematicName>
-<Xref>PDBHET:0AF</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 11 H 10 N 2 O 2</Formula>
-<Weight type="chemical">202.21</Weight>
-<Weight type="physical">202.074228</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0018">
-<Formula>C 0 H 0 N 0 O 1</Formula>
-<Weight type="chemical">16.00</Weight>
-<Weight type="physical">15.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Jensen, L.M.</Author>
-<Author>Sanishvili, R.</Author>
-<Author>Davidson, V.L.</Author>
-<Author>Wilmot, C.M.</Author>
-</Authors>
-<Citation>Science 327, 1392-1394, 2010</Citation>
-<Title>In crystallo posttranslational modification within a MauG/pre-methylamine dehydrogenase complex.</Title>
-<Xref>DOI:10.1126/science.1182492</Xref>
-<Xref>PMID:20223990</Xref>
-<Note>X-ray diffraction, 2.1 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Jensen, L.M.</Author>
-<Author>Wilmot, C.M.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, December 2009</Citation>
-<Description>Crystal structure of the MauG/pre-methylamine dehydrogenase complex.</Description>
-<Xref>PDB:3L4M</Xref>
-<Note>X-ray diffraction, 2.1 angstroms; this previously modified tryptophan is one of the two substrate residues of the enzyme</Note>
-</ReferenceBlock>
-<Comment>This modification without secondary glycosylation (see RESID:AA0506) has only been observed as the first precursor form of 4'-(L-tryptophan)-L-tryptophyl quinone (see RESID:AA0149).</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptidyl-tryptophan 7-oxygenase MauX (EC 1.-.-.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>W</SequenceSpec>
-<Xref>PSI-MOD:01664</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt" key="mod_res__7'-hydroxytryptophan__w">MOD_RES 7'-hydroxytryptophan</Feature>
-<Note>this modification does not occur in UniProt features without secondary modifications</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0520.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0520.PDB" />
-</Entry>
-<Entry id="AA0521">
-<Header>
-<Code>AA0521</Code>
-<Dates>
-<CreationDate>31-Mar-2010</CreationDate>
-<StrucRevDate>31-Mar-2010</StrucRevDate>
-<TextChngDate>30-Sep-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-(DNA-1',2'-dideoxyribos-1'-ylidene)-L-valine</Name>
-<AlternateName>DNA glycosylase valine Schiff base intermediate</AlternateName>
-<SystematicName>(2S)-2-[(3R,4R)-3,4-dihydroxy-5-(phosphonooxy)pentylidene]amino-3-methylbutanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 10 H 17 N 1 O 6 P 1</Formula>
-<Weight type="chemical">278.22</Weight>
-<Weight type="physical">278.079349</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0020">
-<Formula>C 5 H 7 N 0 O 5 P 1</Formula>
-<Weight type="chemical">178.08</Weight>
-<Weight type="physical">178.003110</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Liu, M.</Author>
-<Author>Bandaru, V.</Author>
-<Author>Bond, J.P.</Author>
-<Author>Jaruga, P.</Author>
-<Author>Zhao, X.</Author>
-<Author>Christov, P.P.</Author>
-<Author>Burrows, C.J.</Author>
-<Author>Rizzo, C.J.</Author>
-<Author>Dizdaroglu, M.</Author>
-<Author>Wallace, S.S.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 107, 4925-4930, 2010</Citation>
-<Title>The mouse ortholog of NEIL3 is a functional DNA glycosylase in vitro and in vivo.</Title>
-<Xref>DOI:10.1073/pnas.0908307107</Xref>
-<Xref>PMID:20185759</Xref>
-<Note>chemical evidence of N-terminal valine linkage to DNA</Note>
-</ReferenceBlock>
-<Comment>The model has three open valences, one on the valine carboxyl group and two in the DNA nucleotide segment on the 5'-phosphate and the 3'-hydroxyl.</Comment>
-<Comment>The keyword "phosphoprotein" is not used with polynucleotide-linked intermediate modifications.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>DNA glycosylase (EC 3.2.2.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>V</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>PSI-MOD:01665</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>*phosphoprotein</Keyword>
-<Keyword>blocked amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="act_site__schiff-base intermediate with dna; via amino nitrogen__v">ACT_SITE Schiff-base intermediate with DNA; via amino nitrogen</Feature>
-</Features>
-<Image src="/images/AA0521.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0521.PDB" />
-</Entry>
-<Entry id="AA0522">
-<Header>
-<Code>AA0522</Code>
-<Dates>
-<CreationDate>30-Apr-2010</CreationDate>
-<StrucRevDate>30-Apr-2010</StrucRevDate>
-<TextChngDate>30-Apr-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O4-(8alpha-FAD)-L-aspartate</Name>
-<AlternateName>8alpha-[(4-aspartyl)oxy]FAD</AlternateName>
-<SystematicName>(2S)-2-amino-4-oxo-4-[8alpha-riboflavin 5'-(trihydrogen diphosphate) 5'->5'-ester with adenosine]oxybutanoic acid</SystematicName>
-<Xref>PDBHET:FAD</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 31 H 36 N 10 O 18 P 2</Formula>
-<Weight type="chemical">898.63</Weight>
-<Weight type="physical">898.168428</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0004">
-<Formula>C 27 H 31 N 9 O 15 P 2</Formula>
-<Weight type="chemical">783.54</Weight>
-<Weight type="physical">783.141485</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Podzelinska, K.</Author>
-<Author>Latimer, R.</Author>
-<Author>Bhattacharya, A.</Author>
-<Author>Vining, L.C.</Author>
-<Author>Zechel, D.L.</Author>
-<Author>Jia, Z.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 397, 316-331, 2010</Citation>
-<Title>Chloramphenicol biosynthesis: the structure of CmlS, a flavin-dependent halogenase showing a covalent flavin-aspartate bond.</Title>
-<Xref>DOI:10.1016/j.jmb.2010.01.020</Xref>
-<Xref>PMID:20080101</Xref>
-<Note>X-ray diffraction, 2.20 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Podzelinska, K.</Author>
-<Author>Soares, A.</Author>
-<Author>Jia, Z.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, June 2009</Citation>
-<Description>Crystal structure of CmlS, a flavin-dependent halogenase.</Description>
-<Xref>PDB:3I3L</Xref>
-<Note>X-ray diffraction, 2.20 angstroms</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>D</SequenceSpec>
-<Xref>PSI-MOD:01668</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>*phosphoprotein</Keyword>
-<Keyword>FAD</Keyword>
-<Keyword>flavoprotein</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0522.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0522.PDB" />
-</Entry>
-<Entry id="AA0523">
-<Header>
-<Code>AA0523</Code>
-<Dates>
-<CreationDate>30-Apr-2010</CreationDate>
-<StrucRevDate>30-Apr-2010</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N(omega)-,N(omega)-,N(omega')-trimethyl-L-arginine</Name>
-<AlternateName>(2S)-2-amino-5-([(dimethylamino)(methylimino)methyl]amino)pentanoic acid</AlternateName>
-<AlternateName>2-[(4S)-4-amino-5-oxopentyl]-1,1,3-trimethylguanidine</AlternateName>
-<AlternateName>N(G)-trimethylarginine</AlternateName>
-<AlternateName>N5-[(dimethylamino)(imino)methyl]ornithine</AlternateName>
-<SystematicName>(2S)-2-amino-5-([(dimethylamino)(methylamino)methylidene]amino)pentanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 18 N 4 O 1</Formula>
-<Weight type="chemical">198.27</Weight>
-<Weight type="physical">198.148061</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0002">
-<Formula>C 3 H 6 N 0 O 0</Formula>
-<Weight type="chemical">42.08</Weight>
-<Weight type="physical">42.046950</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Patthy, A.</Author>
-<Author>Bajusz, S.</Author>
-<Author>Patthy, L.</Author>
-</Authors>
-<Citation>Acta Biochim. Biophys. Acad. Sci. Hung. 12, 191-196, 1977</Citation>
-<Title>Preparation and characterization of N(G)-mono-, di- and trimethylated arginines.</Title>
-<Xref>PMID:602668</Xref>
-<Note>chemical synthesis; chromatographic detection; the free amino acid was not found in human urine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Pelletier, M.</Author>
-<Author>Xu, Y.</Author>
-<Author>Wang, X.</Author>
-<Author>Zahariev, S.</Author>
-<Author>Pongor, S.</Author>
-<Author>Aletta, J.M.</Author>
-<Author>Read, L.K.</Author>
-</Authors>
-<Citation>Mol. Biochem. Parasitol. 118, 49-59, 2001</Citation>
-<Title>Arginine methylation of a mitochondrial guide RNA binding protein from Trypanosoma brucei.</Title>
-<Xref>DOI:10.1016/S0166-6851(01)00367-X</Xref>
-<Xref>PMID:11704273</Xref>
-<Note>mass spectrometric detection reported in one tryptic peptide of RNA-binding protein 16; the mass difference is reported as 42.981 Da, measured from the neutral parent, spectral data not shown; subsequently, it has not been confirmed or characterized, or detected in other proteins (Laurie K. Read, private communication, 2010)</Note>
-</ReferenceBlock>
-<Comment>No enzyme activities capable of producing this modification under physiological conditions have been reported.</Comment>
-<SequenceCode>
-<SequenceSpec>R</SequenceSpec>
-<Xref>PSI-MOD:01669</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>methylated amino acid</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0523.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0523.PDB" />
-</Entry>
-<Entry id="AA0524">
-<Header>
-<Code>AA0524</Code>
-<Dates>
-<CreationDate>30-Apr-2010</CreationDate>
-<StrucRevDate>30-Apr-2010</StrucRevDate>
-<TextChngDate>30-Apr-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6-chloro-L-lysine</Name>
-<AlternateName>epsilon-chlorolysine</AlternateName>
-<AlternateName>lysine chloramine</AlternateName>
-<AlternateName>N(zeta)-chlorolysine</AlternateName>
-<SystematicName>(2S)-2-amino-6-(chloroamino)hexanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 6 Cl 1 H 11 N 2 O 1</Formula>
-<Weight type="chemical">162.62</Weight>
-<Weight type="physical">162.055991</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 0 Cl 1 H -1 N 0 O 0</Formula>
-<Weight type="chemical">34.44</Weight>
-<Weight type="physical">33.961028</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Peng, D.Q.</Author>
-<Author>Wu, Z.</Author>
-<Author>Brubaker, G.</Author>
-<Author>Zheng, L.</Author>
-<Author>Settle, M.</Author>
-<Author>Gross, E.</Author>
-<Author>Kinter, M.</Author>
-<Author>Hazen, S.L.</Author>
-<Author>Smith, J.D.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 280, 33775-33784, 2005</Citation>
-<Title>Tyrosine modification is not required for myeloperoxidase-induced loss of apolipoprotein A-I functional activities.</Title>
-<Xref>DOI:10.1074/jbc.M504092200</Xref>
-<Xref>PMID:16091367</Xref>
-<Note>conversion of lysine residues to chlorolysine by myeloperoxidase is assayed with 5-thio-2-nitrobenzoic acid (TNB)</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Dong, C.</Author>
-<Author>Flecks, S.</Author>
-<Author>Unversucht, S.</Author>
-<Author>Haupt, C.</Author>
-<Author>van Pée, K.H.</Author>
-<Author>Naismith, J.H.</Author>
-</Authors>
-<Citation>Science 309, 2216-2219, 2005</Citation>
-<Title>Tryptophan 7-halogenase (PrnA) structure suggests a mechanism for regioselective chlorination.</Title>
-<Xref>DOI:10.1126/science.1116510</Xref>
-<Xref>PMID:16195462</Xref>
-<Note>X-ray diffraction, 1.95 angstroms; proposal for a mechanism with hypochlorite bound between lysine and glutamate</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yeh, E.</Author>
-<Author>Blasiak, L.C.</Author>
-<Author>Koglin, A.</Author>
-<Author>Drennan, C.L.</Author>
-<Author>Walsh, C.T.</Author>
-</Authors>
-<Citation>Biochemistry 46, 1284-1292, 2007</Citation>
-<Title>Chlorination by a long-lived intermediate in the mechanism of flavin-dependent halogenases.</Title>
-<Xref>DOI:10.1021/bi0621213</Xref>
-<Xref>PMID:17260957</Xref>
-<Note>X-ray diffraction, 2.08 angstroms; proposal for the formation of lysine chloramine as an intermediate based on the persistence of chlorinating activity after dialysis removal of flavin and chloride; the proposed intermediate is not modeled in the deposited structures</Note>
-</ReferenceBlock>
-<Comment>In tryptophan 7-halogenase (EC 1.14.14.7), the modification is formed by autocatalysis as an intermediate in the catalytic cycle. The formation by myeloperoxidase (EC 1.11.1.7) is probably not a normal metabolic process.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-<EnzymeName>myeloperoxidase (EC 1.11.1.7)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>PSI-MOD:01670</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>chlorine</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0524.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0524.PDB" />
-</Entry>
-<Entry id="AA0525">
-<Header>
-<Code>AA0525</Code>
-<Dates>
-<CreationDate>30-Apr-2010</CreationDate>
-<StrucRevDate>30-Apr-2010</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-(L-isoaspartyl)-L-threonine</Name>
-<AlternateName>(2S,3R)-2-amino-3-([(4S)-3-amino-3-carboxypropanoyl]oxy)propanoic acid</AlternateName>
-<AlternateName>O(beta)-(beta-aspartyl)threonine</AlternateName>
-<AlternateName>O3-(isoaspartyl)-threonine</AlternateName>
-<SystematicName>(2S)-2-amino-4-([(1S,2R)-1-amino-1-carboxypropan-2-yl]oxy)-4-oxobutanoic acid</SystematicName>
-<Xref>PDBHET:AEI</Xref>
-</Names>
-<FormulaBlock label="TDX">
-<Formula>C 8 H 10 N 2 O 4</Formula>
-<Weight type="chemical">198.18</Weight>
-<Weight type="physical">198.064057</Weight>
-</FormulaBlock>
-<FormulaBlock label="THR">
-<Formula>C 8 H 12 N 2 O 5</Formula>
-<Weight type="chemical">216.19</Weight>
-<Weight type="physical">216.074621</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0004 AA0017" link="TDX">
-<Formula>C 0 H -2 N 0 O -1</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0017" link="THR">
-<Formula>C 4 H 5 N 1 O 3</Formula>
-<Weight type="chemical">115.09</Weight>
-<Weight type="physical">115.026943</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ishitsuka, M.O.</Author>
-<Author>Kusumi, T.</Author>
-<Author>Kakisawa, H.</Author>
-<Author>Kaya, K.</Author>
-<Author>Watanabe, M.M.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 112, 8180-8182, 1990</Citation>
-<Title>Microviridin. A novel tricyclic depsipeptide from the toxic cyanobacterium Microcystis viridis.</Title>
-<Xref>DOI:10.1021/ja00178a060</Xref>
-<Note>amino acid composition; (1)H-NMR and (13)C-NMR identification; chemical characterization of the ester cross-links</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Palm, G.J.</Author>
-<Author>Lubkowski, J.</Author>
-<Author>Derst, C.</Author>
-<Author>Schleper, S.</Author>
-<Author>Röhm, K.H.</Author>
-<Author>Wlodawer, A.</Author>
-</Authors>
-<Citation>FEBS Lett. 390, 211-216, 1996</Citation>
-<Title>A covalently bound catalytic intermediate in Escherichia coli asparaginase: crystal structure of a Thr-89-Val mutant.</Title>
-<Xref>DOI:10.1016/0014-5793(96)00660-6</Xref>
-<Xref>PMID:8706862</Xref>
-<Note>X-ray diffraction, 2.20 angstroms; a Thr-89-Val mutant has a trapped covalent intermediate</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Palm, G.J.</Author>
-<Author>Lubkowski, J.</Author>
-<Author>Derst, C.</Author>
-<Author>Wlodawer, A.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, February 1997</Citation>
-<Description>Asparaginase from E. coli, mutant T89V with covalently bound aspartate.</Description>
-<Xref>PDB:4ECA</Xref>
-<Note>X-ray diffraction, 2.20 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wang, Y.</Author>
-<Author>Guo, H.C.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 366, 82-92, 2007</Citation>
-<Title>Crystallographic snapshot of a productive glycosylasparaginase-substrate complex.</Title>
-<Xref>DOI:10.1016/j.jmb.2006.09.051</Xref>
-<Xref>PMID:17157318</Xref>
-<Note>X-ray diffraction, 2.00 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wang, Y.</Author>
-<Author>Guo, H.C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, April 2006</Citation>
-<Description>Crystal structure of glycosylasparaginase-substrate complex.</Description>
-<Xref>PDB:2GL9</Xref>
-<Note>X-ray diffraction, 2.00 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Philmus, B.</Author>
-<Author>Christiansen, G.</Author>
-<Author>Yoshida, W.Y.</Author>
-<Author>Hemscheidt, T.K.</Author>
-</Authors>
-<Citation>Chembiochem 9, 3066-3073, 2008</Citation>
-<Title>Post-translational modification in microviridin biosynthesis.</Title>
-<Xref>DOI:10.1002/cbic.200800560</Xref>
-<Xref>PMID:19035375</Xref>
-<Note>(1)H-NMR and (13)C-NMR analysis; mass spectrometric and chemical characterization; directed mutation analysis; gene sequence for the encoded peptide</Note>
-</ReferenceBlock>
-<Comment>The formula and records labeled "TDX" refers to O3-(isoaspartyl)-threonine produced as an ester cross-link of a peptidyl threonine residue and a peptidyl aspartic acid residue. The ester cross-link is formed by an RimK related enzyme using ATP.</Comment>
-<Comment>The formula and records labeled "THR" refers to O3-(isoaspartyl)-threonine produced as peptidyl threonine residue ester bonded to a free asparagine with the release of ammonia. The isoaspartylation modification of threonine by asparagine is produced by autocatalysis as an intermediate in the catalytic cycle of asparginase.</Comment>
-<GeneratingEnzyme>
-<EnzymeName link="TDX">peptidyl-threonine--peptidyl-aspartate ligase MvdD (EC 6.1.2.-)</EnzymeName>
-<EnzymeName link="THR">autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode link="TDX">
-<SequenceSpec>D, T</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:01947</Xref>
-</SequenceCode>
-<SequenceCode link="THR">
-<SequenceSpec>T</SequenceSpec>
-<Xref>PSI-MOD:01671</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="act_site__o-isoaspartyl threonine intermediate__t" link="THR">ACT_SITE O-isoaspartyl threonine intermediate</Feature>
-<Feature type="UniProt" key="crosslnk__isoaspartyl threonine ester (thr-asp)__t__d" link="TDX">CROSSLNK isoaspartyl threonine ester (Thr-Asp)</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="act_site__acyl-ester intermediate__t" link="THR">ACT_SITE Acyl-ester intermediate</Feature>
-<Note>this ambiguous form is used for enzymes with glutaminase-asparaginase activity</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0525.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0525.PDB" />
-</Entry>
-<Entry id="AA0526">
-<Header>
-<Code>AA0526</Code>
-<Dates>
-<CreationDate>28-May-2010</CreationDate>
-<StrucRevDate>28-May-2010</StrucRevDate>
-<TextChngDate>31-Dec-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-(coelenterazin-3a-yl)-L-cysteine</Name>
-<AlternateName>dehydrocoelenterazine cysteine adduct</AlternateName>
-<AlternateName>symplectin chromophore</AlternateName>
-<SystematicName>(2R)-2-amino-3-([(4-hydroxyphenyl)(8-benzyl-3-oxo-6-[4-hydroxyphenyl]-3,7-dihydroimidazo[1,2-a]pyrazin-2-yl)methyl]sulfanyl)propanoic acid</SystematicName>
-<Xref>CAS:55779-48-1</Xref>
-<Xref>ChEBI:2311</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 29 H 24 N 4 O 4 S 1</Formula>
-<Weight type="chemical">524.60</Weight>
-<Weight type="physical">524.151826</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 26 H 19 N 3 O 3 S 0</Formula>
-<Weight type="chemical">421.46</Weight>
-<Weight type="physical">421.142641</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Isobe, M.</Author>
-<Author>Kuse, M.</Author>
-<Author>Tani, N.</Author>
-<Author>Fujii, T.</Author>
-<Author>Matsuda, T.</Author>
-</Authors>
-<Citation>Proc. Jpn. Acad., Ser. B, Phys. Biol. Sci. 84, 386-392, 2008</Citation>
-<Title>Cysteine-390 is the binding site of luminous substance with symplectin, a photoprotein from Okinawan squid, Symplectoteuthis oualaniensis.</Title>
-<Xref>DOI:10.2183/pjab/84.386</Xref>
-<Xref>PMID:18997450</Xref>
-</ReferenceBlock>
-<Comment>Coelenterazine is one of the four major marine luciferins, being used by various bioluminescent species in at least eight phyla. Coelenterazine may result from modification of a phenylalanyl-tyrosyl-tyrosine peptide produced by an unidentified endosymbiotic organism.  See RESID:AA0595.</Comment>
-<Comment>The chirality of the cysteine adduct has not been determined.</Comment>
-<Comment>This entry presents coelenterazine as a heterogen cross-linked to a cysteine. For coelenterazine as a modification produced by the cross-linking of a tripeptide precursor see RESID:AA0595.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>PSI-MOD:01694</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chromoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__s-(coelenterazin-3a-yl)cysteine__c">MOD_RES S-(coelenterazin-3a-yl)cysteine</Feature>
-</Features>
-<Image src="/images/AA0526.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0526.PDB" />
-</Entry>
-<Entry id="AA0527">
-<Header>
-<Code>AA0527</Code>
-<Dates>
-<CreationDate>30-Jun-2010</CreationDate>
-<StrucRevDate>30-Jun-2010</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6-octanoyl-L-lysine</Name>
-<AlternateName>epsilon-octanoyllysine</AlternateName>
-<AlternateName>N(zeta)-octanoyllysine</AlternateName>
-<AlternateName>N6-(1-oxooctyl)-L-lysine</AlternateName>
-<SystematicName>(2S)-2-amino-6-(octanoylamino)hexanoic acid</SystematicName>
-<Xref>CAS:23735-96-8</Xref>
-<Xref>ChEBI:78809</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 14 H 26 N 2 O 2</Formula>
-<Weight type="chemical">254.37</Weight>
-<Weight type="physical">254.199428</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 8 H 14 N 0 O 1</Formula>
-<Weight type="chemical">126.20</Weight>
-<Weight type="physical">126.104465</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ali, S.T.</Author>
-<Author>Moir, A.J.</Author>
-<Author>Ashton, P.R.</Author>
-<Author>Engel, P.C.</Author>
-<Author>Guest, J.R.</Author>
-</Authors>
-<Citation>Mol. Microbiol. 4, 943-950, 1990</Citation>
-<Title>Octanoylation of the lipoyl domains of the pyruvate dehydrogenase complex in a lipoyl-deficient strain of Escherichia coli.</Title>
-<Xref>DOI:10.1111/j.1365-2958.1990.tb00667.x</Xref>
-<Xref>PMID:2215217</Xref>
-<Note>mass spectrometric detection at the same site as lipoic acid modification in dihydrolipoamide acetyltransferase when it is over-expressed</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Jordan, S.W.</Author>
-<Author>Cronan Jr., J.E.</Author>
-</Authors>
-<Citation>J. Bacteriol. 185, 1582-1589, 2003</Citation>
-<Title>The Escherichia coli lipB gene encodes lipoyl (octanoyl)-acyl carrier protein:protein transferase.</Title>
-<Xref>DOI:10.1128/JB.185.5.1582-1589.2003</Xref>
-<Xref>PMID:12591875</Xref>
-<Note>identification of enzyme activity for the modification</Note>
-</ReferenceBlock>
-<Comment>The metabolic role of this modification is uncertain.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>octanoyltransferase (EC 2.3.1.181)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>PSI-MOD:01774</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lipoprotein</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0527.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0527.PDB" />
-</Entry>
-<Entry id="AA0528">
-<Header>
-<Code>AA0528</Code>
-<Dates>
-<CreationDate>30-Jun-2010</CreationDate>
-<StrucRevDate>30-Jun-2010</StrucRevDate>
-<TextChngDate>31-May-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>5-glutamyl serotonin</Name>
-<AlternateName>N2-(gamma-glutamyl)-5-hydoxytryptamine</AlternateName>
-<AlternateName>N5-[2-(5-hydroxy-3-indolyl)ethyl]glutamine</AlternateName>
-<SystematicName>(2S)-2-amino-5-([2-(5-hydroxy-1H-indol-3-yl)ethyl]amino)-5-oxopentanoic acid</SystematicName>
-<Xref>CAS:61059-62-9</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 15 H 17 N 3 O 3</Formula>
-<Weight type="chemical">287.32</Weight>
-<Weight type="physical">287.126991</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0007">
-<Formula>C 10 H 9 N 1 O 1</Formula>
-<Weight type="chemical">159.19</Weight>
-<Weight type="physical">159.068414</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Dale, G.L.</Author>
-<Author>Friese, P.</Author>
-<Author>Batar, P.</Author>
-<Author>Hamilton, S.F.</Author>
-<Author>Reed, G.L.</Author>
-<Author>Jackson, K.W.</Author>
-<Author>Clemetson, K.J.</Author>
-<Author>Alberio, L.</Author>
-</Authors>
-<Citation>Nature 415, 175-179, 2002</Citation>
-<Title>Stimulated platelets use serotonin to enhance their retention of procoagulant proteins on the cell surface.</Title>
-<Xref>DOI:10.1038/415175a</Xref>
-<Xref>PMID:11805836</Xref>
-<Note>chromatographic detection on COAT-platelet alpha-granule proteins after hydrolysis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Walther, D.J.</Author>
-<Author>Peter, J.U.</Author>
-<Author>Winter, S.</Author>
-<Author>Höltje, M.</Author>
-<Author>Paulmann, N.</Author>
-<Author>Grohmann, M.</Author>
-<Author>Vowinckel, J.</Author>
-<Author>Alamo-Bethencourt, V.</Author>
-<Author>Wilhelm, C.S.</Author>
-<Author>Ahnert-Hilger, G.</Author>
-<Author>Bader, M.</Author>
-</Authors>
-<Citation>Cell 115, 851-862, 2003</Citation>
-<Title>Serotonylation of small GTPases is a signal transduction pathway that triggers platelet alpha-granule release.</Title>
-<Xref>DOI:10.1016/S0092-8674(03)01014-6</Xref>
-<Xref>PMID:14697203</Xref>
-<Note>radiolabeling demonstrates serotonin transamidation to RhoA and small GTPases during activation; glutamine-63 is suggested, but not demonstrated, to be transamidated by serotonin</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lin, J.C.</Author>
-<Author>Chou, C.C.</Author>
-<Author>Gao, S.</Author>
-<Author>Wu, S.C.</Author>
-<Author>Khoo, K.H.</Author>
-<Author>Lin, C.H.</Author>
-</Authors>
-<Citation>Chembiochem 14, 813-817, 2013</Citation>
-<Title>An in Vivo Tagging Method Reveals that Ras Undergoes Sustained Activation upon Transglutaminase-Mediated Protein Serotonylation.</Title>
-<Xref>DOI:10.1002/cbic.201300050</Xref>
-<Xref>PMID:23592595</Xref>
-<Note>chemical derivatization; mass spectrometric identification and localization</Note>
-</ReferenceBlock>
-<Comment>The structure shown in PubChem for this name is incorrect being instead alpha-glutamyl serotonin, which is not the product of transamidation.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>protein-glutamine gamma-glutamyltransferase (EC 2.3.2.13)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>Q</SequenceSpec>
-<Xref>PSI-MOD:01775</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>serotonylation</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0528.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0528.PDB" />
-</Entry>
-<Entry id="AA0529">
-<Header>
-<Code>AA0529</Code>
-<Dates>
-<CreationDate>30-Sep-2010</CreationDate>
-<StrucRevDate>30-Sep-2010</StrucRevDate>
-<TextChngDate>30-Sep-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-(glycyl)-L-cysteine</Name>
-<AlternateName>N-(2-amino-1-oxoethyl)cysteine</AlternateName>
-<SystematicName>(2R)-2-[(aminoacetyl)amino]-3-sulfanylpropanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 9 N 2 O 3 S 1</Formula>
-<Weight type="chemical">177.20</Weight>
-<Weight type="physical">177.033388</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0008">
-<Formula>C 3 H 5 N 1 O 1 S 1</Formula>
-<Weight type="chemical">103.14</Weight>
-<Weight type="physical">103.009185</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ågren, D.</Author>
-<Author>Schnell, R.</Author>
-<Author>Oehlmann, W.</Author>
-<Author>Singh, M.</Author>
-<Author>Schneider, G.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 283, 31567-31574, 2008</Citation>
-<Title>Cysteine synthase (CysM) of Mycobacterium tuberculosis is an O-phosphoserine sulfhydrylase: evidence for an alternative cysteine biosynthesis pathway in mycobacteria.</Title>
-<Xref>DOI:10.1074/jbc.M804877200</Xref>
-<Xref>PMID:18799456</Xref>
-<Note>the encoding of an author's name in the PubMed citation is corrected to UTF8</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Jurgenson, C.T.</Author>
-<Author>Burns, K.E.</Author>
-<Author>Begley, T.P.</Author>
-<Author>Ealick, S.E.</Author>
-</Authors>
-<Citation>Biochemistry 47, 10354-10364, 2008</Citation>
-<Title>Crystal structure of a sulfur carrier protein complex found in the cysteine biosynthetic pathway of Mycobacterium tuberculosis.</Title>
-<Xref>DOI:10.1021/bi800915j</Xref>
-<Xref>PMID:18771296</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>O'Leary, S.E.</Author>
-<Author>Jurgenson, C.T.</Author>
-<Author>Ealick, S.E.</Author>
-<Author>Begley, T.P.</Author>
-</Authors>
-<Citation>Biochemistry 47, 11606-11615, 2008</Citation>
-<Title>O-phospho-L-serine and the thiocarboxylated sulfur carrier protein CysO-COSH are substrates for CysM, a cysteine synthase from Mycobacterium tuberculosis.</Title>
-<Xref>DOI:10.1021/bi8013664</Xref>
-<Xref>PMID:18842002</Xref>
-<Note>cysteine thioester linked to a carboxyl terminal glycine is formed by condensation of a carboxyl terminal thioglycine with free phosphoserine</Note>
-</ReferenceBlock>
-<Comment>This modified carboxyl end glycine residue is produced by transamidation of S-(glycyl)-L-cysteine (see RESID:AA0206) transiently forming a peptide bond to a free cysteine before the cysteine is released by a peptidase activity.</Comment>
-<SequenceCode>
-<SequenceSpec>G</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Xref>PSI-MOD:01778</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__cyso-cysteine adduct__g">MOD_RES CysO-cysteine adduct</Feature>
-</Features>
-<Image src="/images/AA0529.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0529.PDB" />
-</Entry>
-<Entry id="AA0530">
-<Header>
-<Code>AA0530</Code>
-<Dates>
-<CreationDate>30-Sep-2010</CreationDate>
-<StrucRevDate>30-Sep-2010</StrucRevDate>
-<TextChngDate>01-Mar-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6-(L-lysyl)-L-lysine</Name>
-<AlternateName>N6-(alpha-lysyl)-lysine</AlternateName>
-<SystematicName>(2S)-2-amino-6-([(2S)-2,6-diaminohexanoyl]amino)hexanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 12 H 24 N 4 O 2</Formula>
-<Weight type="chemical">256.35</Weight>
-<Weight type="physical">256.189926</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 6 H 12 N 2 O 1</Formula>
-<Weight type="chemical">128.18</Weight>
-<Weight type="physical">128.094963</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Aoki, H.</Author>
-<Author>Xu, J.</Author>
-<Author>Emili, A.</Author>
-<Author>Chosay, J.G.</Author>
-<Author>Golshani, A.</Author>
-<Author>Ganoza, M.C.</Author>
-</Authors>
-<Citation>FEBS J. 275, 671-681, 2008</Citation>
-<Title>Interactions of elongation factor EF-P with the Escherichia coli ribosome.</Title>
-<Xref>DOI:10.1111/j.1742-4658.2007.06228.x</Xref>
-<Xref>PMID:18201202</Xref>
-<Note>mass spectrometric detection of a modification with a change in mass of 143.8 Da probably at Lys-34; proposed to be a spermidine derivative</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yanagisawa, T.</Author>
-<Author>Sumida, T.</Author>
-<Author>Ishii, R.</Author>
-<Author>Takemoto, C.</Author>
-<Author>Yokoyama, S.</Author>
-</Authors>
-<Citation>Nature Struct. Mol. Biol. 17, 1136-1143, 2010</Citation>
-<Title>A paralog of lysyl-tRNA synthetase aminoacylates a conserved lysine residue in translation elongation factor P.</Title>
-<Xref>DOI:10.1038/nsmb.1889</Xref>
-<Xref>PMID:20729861</Xref>
-<Note>mass spectrometric detection of a modification with a change in mass of 127.7 Da at Lys-34; identified as probably being N6-(L-lysyl)-L-lysine produced by enzymatic transfer from lysyl-tRNA</Note>
-</ReferenceBlock>
-<Comment>This modification occurs transiently in prokaryotic elogation factor P during production of the mature protein. For the mature form of the EF-P modification, see RESID:AA0531.</Comment>
-<Comment>The modified lysine residue is homologous to the lysine modified to hypusine (see RESID:AA0116) in eukaryotic and archaeal translation initiation factor 5A.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>translation elongation factor P-lysine N6-lysyltransferase YjeA (EC 2.3.2.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>GO:0071915</Xref>
-<Xref>GO:0072580</Xref>
-<Xref>PSI-MOD:01779</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0530.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0530.PDB" />
-</Entry>
-<Entry id="AA0531">
-<Header>
-<Code>AA0531</Code>
-<Dates>
-<CreationDate>30-Sep-2010</CreationDate>
-<StrucRevDate>24-Aug-2012</StrucRevDate>
-<TextChngDate>31-Dec-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>5-hydroxy-N6-(beta-lysyl)-L-lysine</Name>
-<AlternateName>5-hydroxy-N6-[(3R)-beta-lysyl]lysine</AlternateName>
-<AlternateName>EF-P lysine derivative</AlternateName>
-<AlternateName>lysyl spermidine derivative [misidentification]</AlternateName>
-<AlternateName>N6-[(3R)-3,6-diaminohexanoyl]-L-5-hydroxylysine</AlternateName>
-<SystematicName>(2S)-2-amino-6-([(3R)-3,6-diaminohexanoyl]amino)-5-hydroxyhexanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 12 H 24 N 4 O 3</Formula>
-<Weight type="chemical">272.35</Weight>
-<Weight type="physical">272.184841</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 6 H 12 N 2 O 2</Formula>
-<Weight type="chemical">144.17</Weight>
-<Weight type="physical">144.089878</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Aoki, H.</Author>
-<Author>Xu, J.</Author>
-<Author>Emili, A.</Author>
-<Author>Chosay, J.G.</Author>
-<Author>Golshani, A.</Author>
-<Author>Ganoza, M.C.</Author>
-</Authors>
-<Citation>FEBS J. 275, 671-681, 2008</Citation>
-<Title>Interactions of elongation factor EF-P with the Escherichia coli ribosome.</Title>
-<Xref>DOI:10.1111/j.1742-4658.2007.06228.x</Xref>
-<Xref>PMID:18201202</Xref>
-<Note>mass spectrometric detection of a modification with a change in mass of 143.8 Da probably at Lys-34; proposed to be a spermidine derivative</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yanagisawa, T.</Author>
-<Author>Sumida, T.</Author>
-<Author>Ishii, R.</Author>
-<Author>Takemoto, C.</Author>
-<Author>Yokoyama, S.</Author>
-</Authors>
-<Citation>Nature Struct. Mol. Biol. 17, 1136-1143, 2010</Citation>
-<Title>A paralog of lysyl-tRNA synthetase aminoacylates a conserved lysine residue in translation elongation factor P.</Title>
-<Xref>DOI:10.1038/nsmb.1889</Xref>
-<Xref>PMID:20729861</Xref>
-<Note>mass spectrometric detection of a modification with a change in mass of 127.7 Da at Lys-34; isobaric product of N6-(L-lysyl)-L-lysine produced by an enzyme similar to lysine 2,3-aminomutase.</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Roy, H.</Author>
-<Author>Zou, S.B.</Author>
-<Author>Bullwinkle, T.J.</Author>
-<Author>Wolfe, B.S.</Author>
-<Author>Gilreath, M.S.</Author>
-<Author>Forsyth, C.J.</Author>
-<Author>Navarre, W.W.</Author>
-<Author>Ibba, M.</Author>
-</Authors>
-<Citation>Nature Chem. Biol. 7, 667-669, 2011</Citation>
-<Title>The tRNA synthetase paralog PoxA modifies elongation factor-P with (R)-beta-lysine.</Title>
-<Xref>DOI:10.1038/nchembio.632</Xref>
-<Xref>PMID:21841797</Xref>
-<Note>enzyme kinetics suggests that the preferred substrate for (3R)-beta-lysine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Peil, L.</Author>
-<Author>Starosta, A.L..</Author>
-<Author>Virumäe, K.</Author>
-<Author>Atkinson, G.C.</Author>
-<Author>Tenson, T.</Author>
-<Author>Remme, J.</Author>
-<Author>Wilson, D.N.</Author>
-</Authors>
-<Citation>Nature Chem. Biol. 8, 695-697, 2012</Citation>
-<Title>Lys34 of translation elongation factor EF-P is hydroxylated by YfcM.</Title>
-<Xref>DOI:10.1038/nchembio.1001</Xref>
-<Xref>PMID:22706199</Xref>
-<Note>mass spectrometric identification; radiolabeling</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ude, S.</Author>
-<Author>Lassak, J.</Author>
-<Author>Starosta, A.L.</Author>
-<Author>Kraxenberger, T.</Author>
-<Author>Wilson, D.N.</Author>
-<Author>Jung, K.</Author>
-</Authors>
-<Citation>Science 339, 82-85, 2013</Citation>
-<Title>Translation elongation factor EF-P alleviates ribosome stalling at polyproline stretches.</Title>
-<Xref>DOI:10.1126/science.1228985</Xref>
-<Xref>PMID:23239623</Xref>
-<Note>determination of function</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Doerfel, L.K.</Author>
-<Author>Wohlgemuth, I.</Author>
-<Author>Kothe, C.</Author>
-<Author>Peske, F.</Author>
-<Author>Urlaub, H.</Author>
-<Author>Rodnina, M.V.</Author>
-</Authors>
-<Citation>Science 339, 85-88, 2013</Citation>
-<Title>EF-P is essential for rapid synthesis of proteins containing consecutive proline residues.</Title>
-<Xref>DOI:10.1126/science.1229017</Xref>
-<Xref>PMID:23239624</Xref>
-<Note>determination of function</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yanagisawa, T.</Author>
-<Author>Sumida, T.</Author>
-<Author>Ishii, R.</Author>
-<Author>Takemoto, C.</Author>
-<Author>Yokoyama, S.</Author>
-</Authors>
-<Citation>Nature Struct. Mol. Biol. 17, 1136-1143, 2010</Citation>
-<Title>A paralog of lysyl-tRNA synthetase aminoacylates a conserved lysine residue in translation elongation factor P.</Title>
-<Xref>DOI:10.1038/nsmb.1889</Xref>
-<Xref>PMID:20729861</Xref>
-<Note>mass spectrometric detection</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sumida, T.</Author>
-<Author>Yanagisawa, T.</Author>
-<Author>Ishii, R.</Author>
-<Author>Yokoyama, S.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, August 2009</Citation>
-<Description>Crystal Structure of Escherichia coli GenX in complex with elongation factor P.</Description>
-<Xref>PDB:3A5Z</Xref>
-<Note>X-ray diffraction, 2.50 angstroms</Note>
-</ReferenceBlock>
-<Comment>This modification is produced from N6-acylation of lysine by a lysyl-adenylate. However, evidence on whether alpha- or beta-lysyl adenylate is used, and the intermediates on the pathway appears to be in conflict (see RESID:AA0530). The modified lysine residue is homologous to the lysine modified to hypusine in eukaryotic and archaeal translation initiation factor 5A.</Comment>
-<Comment>The structure of this modification has not been established. The original proposed structure was not hydroxylated. Neither the location of the hydroxyl, shown as a 5-hydroxy, or its stereochemistry is known.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>translation elongation factor P-lysine 2,3-aminomutase YjeK (EC 5.4.3.-)</EnzymeName>
-<EnzymeName>translation elongation factor P-lysine monooxygenase YfcM (EC 1.14.99.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>GO:0072580</Xref>
-<Xref>GO:0072581</Xref>
-<Xref>PSI-MOD:01780</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Features>
-<Feature type="UniProt" key="mod_res__n6-(3,6-diaminohexanoyl)-5-hydroxylysine__k">MOD_RES N6-(3,6-diaminohexanoyl)-5-hydroxylysine</Feature>
-</Features>
-<Image src="/images/AA0531.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0531.PDB" />
-</Entry>
-<Entry id="AA0532">
-<Header>
-<Code>AA0532</Code>
-<Dates>
-<CreationDate>30-Sep-2010</CreationDate>
-<StrucRevDate>30-Sep-2010</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6-butanoyl-L-lysine</Name>
-<AlternateName>(2S)-2-azanyl-6-(butanoylamino)hexanoic acid</AlternateName>
-<AlternateName>2-amino-6-butyrylaminocaproic acid</AlternateName>
-<AlternateName>epsilon-butanoyl-L-lysine</AlternateName>
-<AlternateName>epsilon-butyryl-L-lysine</AlternateName>
-<AlternateName>N(zeta)-butanoyllysine</AlternateName>
-<AlternateName>N6-(1-oxobutyl)-L-lysine</AlternateName>
-<AlternateName>N6-butyryllysine</AlternateName>
-<SystematicName>(2S)-2-amino-6-(butanoylamino)hexanoic acid</SystematicName>
-<Xref>PDBHET:BTK</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 10 H 18 N 2 O 2</Formula>
-<Weight type="chemical">198.27</Weight>
-<Weight type="physical">198.136828</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 4 H 6 N 0 O 1</Formula>
-<Weight type="chemical">70.09</Weight>
-<Weight type="physical">70.041865</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Chen, Y.</Author>
-<Author>Sprung, R.</Author>
-<Author>Tang, Y.</Author>
-<Author>Ball, H.</Author>
-<Author>Sangras, B.</Author>
-<Author>Kim, S.C.</Author>
-<Author>Falck, J.R.</Author>
-<Author>Peng, J.</Author>
-<Author>Gu, W.</Author>
-<Author>Zhao, Y.</Author>
-</Authors>
-<Citation>Mol. Cell. Proteomics 6, 812-819, 2007</Citation>
-<Title>Lysine propionylation and butyrylation are novel post-translational modifications in histones.</Title>
-<Xref>DOI:10.1074/mcp.M700021-MCP200</Xref>
-<Xref>PMID:17267393</Xref>
-<Note>the modification is not chemically characterized and isobaric alternatives are not eliminated</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Vollmuth, F.</Author>
-<Author>Geyer, M.</Author>
-</Authors>
-<Citation>Angew. Chem. Int. Ed. Engl. 49, 6768-6772, 2010</Citation>
-<Title>Interaction of propionylated and butyrylated histone H3 lysine marks with Brd4 bromodomains.</Title>
-<Xref>DOI:10.1002/anie.201002724</Xref>
-<Xref>PMID:20715035</Xref>
-<Note>X-ray diffraction, 1.65 angstroms; iosthermal titration calorimetry; binding of butanoylated lysine histone peptide is found to be unspecific and too weak to be measured as compared with the corresponding acetylated peptide</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Vollmuth, V.</Author>
-<Author>Geyer, M.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, May 2010</Citation>
-<Description>Crystal structure of Brd4 bromodomain 1 with butyrylated histone H3-K(buty)14.</Description>
-<Xref>PDB:3MUL</Xref>
-<Note>X-ray diffraction, 1.65 angstroms</Note>
-</ReferenceBlock>
-<Comment>A metabolic source for butanoic acid in the nucleus is not evident, and a responsible generating enzyme activity is not identified.</Comment>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>PSI-MOD:01781</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>lipoprotein</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0532.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0532.PDB" />
-</Entry>
-<Entry id="AA0533">
-<Header>
-<Code>AA0533</Code>
-<Dates>
-<CreationDate>30-Sep-2010</CreationDate>
-<StrucRevDate>30-Sep-2010</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-methyl-L-serine</Name>
-<AlternateName>N-methylserine</AlternateName>
-<SystematicName>(2S)-3-hydroxy-2-(methylamino)propanoic acid</SystematicName>
-<Xref>CAS:2480-26-4</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 7 N 1 O 2</Formula>
-<Weight type="chemical">101.10</Weight>
-<Weight type="physical">101.047678</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 1 H 2 N 0 O 0</Formula>
-<Weight type="chemical">14.03</Weight>
-<Weight type="physical">14.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Tooley, C.E.</Author>
-<Author>Petkowski, J.J.</Author>
-<Author>Muratore-Schroeder, T.L.</Author>
-<Author>Balsbaugh, J.L.</Author>
-<Author>Shabanowitz, J.</Author>
-<Author>Sabat, M.</Author>
-<Author>Minor, W.</Author>
-<Author>Hunt, D.F.</Author>
-<Author>Macara, I.G.</Author>
-</Authors>
-<Citation>Nature 466, 1125-1128, 2010</Citation>
-<Title>NRMT is an alpha-N-methyltransferase that methylates RCC1 and retinoblastoma protein.</Title>
-<Xref>DOI:10.1038/nature09343</Xref>
-<Xref>PMID:20668449</Xref>
-</ReferenceBlock>
-<Comment>Polypeptides with monomethylated amino terminals can undergo premature cleavage during the coupling step of an Edman degradation. This can result in "preview" with both a residue and the following residue being seen from the first step on through a sequence.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>N-terminal RCC1 methyltransferase</EnzymeName>
-<EnzymeName>protein N-terminal methyltransferase</EnzymeName>
-<EnzymeName>S-adenosyl-L-methionine:N-terminal-(A,P,S)PK-[protein] methyltransferase (EC 2.1.1.244)</EnzymeName>
-<EnzymeName>protein N-terminal monomethyltransferase</EnzymeName>
-<EnzymeName>S-adenosyl-L-methionine:N-terminal-(A,P,S)PK-[protein] monomethyltransferase (EC 2.1.1.299)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>GO:0035570</Xref>
-<Xref>GO:0035571</Xref>
-<Xref>PSI-MOD:01782</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>methylated amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n-methylserine__s">MOD_RES N-methylserine</Feature>
-</Features>
-<Image src="/images/AA0533.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0533.PDB" />
-</Entry>
-<Entry id="AA0534">
-<Header>
-<Code>AA0534</Code>
-<Dates>
-<CreationDate>30-Sep-2010</CreationDate>
-<StrucRevDate>30-Sep-2010</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N,N-dimethyl-L-serine</Name>
-<AlternateName>N,N-dimethylserine</AlternateName>
-<SystematicName>(2S)-2-(dimethylamino)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 10 N 1 O 2</Formula>
-<Weight type="chemical">116.14</Weight>
-<Weight type="physical">116.071154</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 2 H 4 N 0 O 0</Formula>
-<Weight type="chemical">28.05</Weight>
-<Weight type="physical">28.031300</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Tooley, C.E.</Author>
-<Author>Petkowski, J.J.</Author>
-<Author>Muratore-Schroeder, T.L.</Author>
-<Author>Balsbaugh, J.L.</Author>
-<Author>Shabanowitz, J.</Author>
-<Author>Sabat, M.</Author>
-<Author>Minor, W.</Author>
-<Author>Hunt, D.F.</Author>
-<Author>Macara, I.G.</Author>
-</Authors>
-<Citation>Nature 466, 1125-1128, 2010</Citation>
-<Title>NRMT is an alpha-N-methyltransferase that methylates RCC1 and retinoblastoma protein.</Title>
-<Xref>DOI:10.1038/nature09343</Xref>
-<Xref>PMID:20668449</Xref>
-</ReferenceBlock>
-<Comment>For alpha-aino acids, both N-alpha-monomethylation, and N-alpha protonation and complete trimethylation have been observed, but incomplete dimethylation has not been reported as the end result of a natural process.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>N-terminal RCC1 methyltransferase</EnzymeName>
-<EnzymeName>protein N-terminal methyltransferase</EnzymeName>
-<EnzymeName>S-adenosyl-L-methionine:N-terminal-(A,P,S)PK-[protein] methyltransferase (EC 2.1.1.244)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0035570</Xref>
-<Xref>GO:0035572</Xref>
-<Xref>PSI-MOD:01783</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-<Keyword>methylated amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n,n-dimethylserine__s">MOD_RES N,N-dimethylserine</Feature>
-</Features>
-<Image src="/images/AA0534.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0534.PDB" />
-</Entry>
-<Entry id="AA0535">
-<Header>
-<Code>AA0535</Code>
-<Dates>
-<CreationDate>30-Sep-2010</CreationDate>
-<StrucRevDate>30-Sep-2010</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N,N,N-trimethyl-L-serine</Name>
-<AlternateName>(1S)-1-carboxy-2-hydroxy-N,N,N-trimethylethanazanium</AlternateName>
-<AlternateName>(2S)-2-trimethylammonio-3-hydroxypropanoic acid</AlternateName>
-<AlternateName>N,N,N-trimethylserine cation</AlternateName>
-<AlternateName>N,N,N-trimethylserinium</AlternateName>
-<SystematicName>(1S)-1-carboxy-2-hydroxy-N,N,N-trimethylethanaminium</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 13 N 1 O 2</Formula>
-<FormalCharge>1+</FormalCharge>
-<Weight type="chemical">131.17</Weight>
-<Weight type="physical">131.094080</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 3 H 7 N 0 O 0</Formula>
-<FormalCharge>1+</FormalCharge>
-<Weight type="chemical">43.09</Weight>
-<Weight type="physical">43.054227</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Henry, G.D.</Author>
-<Author>Trayer, I.P.</Author>
-<Author>Brewer, S.</Author>
-<Author>Levine, B.A.</Author>
-</Authors>
-<Citation>Eur. J. Biochem. 148, 75-82, 1985</Citation>
-<Title>The widespread distribution of alpha-N-trimethylalanine as the N-terminal amino acid of light chains from vertebrate striated muscle myosins.</Title>
-<Xref>DOI:10.1111/j.1432-1033.1985.tb08809.x</Xref>
-<Xref>PMID:3979397</Xref>
-<Note>(1)H-NMR detection of N,N,N-trimethylated amino terminal "slightly downfield" of N,N,N-trimethylalanine in bovine cardiac myosin regulatory light chain 2, see UniProtKB:Q3SZE5</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Tooley, C.E.</Author>
-<Author>Petkowski, J.J.</Author>
-<Author>Muratore-Schroeder, T.L.</Author>
-<Author>Balsbaugh, J.L.</Author>
-<Author>Shabanowitz, J.</Author>
-<Author>Sabat, M.</Author>
-<Author>Minor, W.</Author>
-<Author>Hunt, D.F.</Author>
-<Author>Macara, I.G.</Author>
-</Authors>
-<Citation>Nature 466, 1125-1128, 2010</Citation>
-<Title>NRMT is an alpha-N-methyltransferase that methylates RCC1 and retinoblastoma protein.</Title>
-<Xref>DOI:10.1038/nature09343</Xref>
-<Xref>PMID:20668449</Xref>
-</ReferenceBlock>
-<Comment>Consult FAQ at http://pir.georgetown.edu/resid/faq.shtml#q12 concerning calculation of the difference formula.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>N-terminal RCC1 methyltransferase</EnzymeName>
-<EnzymeName>protein N-terminal methyltransferase</EnzymeName>
-<EnzymeName>S-adenosyl-L-methionine:N-terminal-(A,P,S)PK-[protein] methyltransferase (EC 2.1.1.244)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>GO:0035570</Xref>
-<Xref>GO:0035573</Xref>
-<Xref>PSI-MOD:01784</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-<Keyword>methylated amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n,n,n-trimethylserine__s">MOD_RES N,N,N-trimethylserine</Feature>
-</Features>
-<Image src="/images/AA0535.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0535.PDB" />
-</Entry>
-<Entry id="AA0536">
-<Header>
-<Code>AA0536</Code>
-<Dates>
-<CreationDate>30-Sep-2010</CreationDate>
-<StrucRevDate>13-Sep-2013</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-(L-isoglutamyl)-L-threonine</Name>
-<AlternateName>(2S,3R)-2-amino-3-([(4S)-4-amino-4-carboxybutanoyl]oxy)-propanoic acid</AlternateName>
-<AlternateName>5-(threon-O3-yl)glutamate</AlternateName>
-<AlternateName>O(beta)-(gamma-glutamyl)threonine</AlternateName>
-<AlternateName>O3-(isoglutamyl)threonine</AlternateName>
-<SystematicName>(2S)-2-amino-5-([(1S,2R)-1-amino-1-carboxypropan-2-yl]oxy)-5-oxopentanoic acid</SystematicName>
-</Names>
-<FormulaBlock label="THR">
-<Formula>C 9 H 14 N 2 O 5</Formula>
-<Weight type="chemical">230.22</Weight>
-<Weight type="physical">230.090272</Weight>
-</FormulaBlock>
-<FormulaBlock label="TQX">
-<Formula>C 9 H 12 N 2 O 4</Formula>
-<Weight type="chemical">212.20</Weight>
-<Weight type="physical">212.079707</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0017" link="THR">
-<Formula>C 5 H 7 N 1 O 3</Formula>
-<Weight type="chemical">129.12</Weight>
-<Weight type="physical">129.042593</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0007 AA0017" link="TQX">
-<Formula>C 0 H -3 N -1 O 0</Formula>
-<Weight type="chemical">-17.03</Weight>
-<Weight type="physical">-17.026549</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Palm, G.J.</Author>
-<Author>Lubkowski, J.</Author>
-<Author>Derst, C.</Author>
-<Author>Schleper, S.</Author>
-<Author>Röhm, K.H.</Author>
-<Author>Wlodawer, A.</Author>
-</Authors>
-<Citation>FEBS Lett. 390, 211-216, 1996</Citation>
-<Title>A covalently bound catalytic intermediate in Escherichia coli asparaginase: crystal structure of a Thr-89-Val mutant.</Title>
-<Xref>DOI:10.1016/0014-5793(96)00660-6</Xref>
-<Xref>PMID:8706862</Xref>
-<Note>X-ray diffraction, 2.20 angstroms; a Thr-89-Val mutant has a trapped covalent intermediate</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Inoue, M.</Author>
-<Author>Hiratake, J.</Author>
-<Author>Suzuki, H.</Author>
-<Author>Kumagai, H.</Author>
-<Author>Sakata, K.</Author>
-</Authors>
-<Citation>Biochemistry 39, 7764-7771, 2000</Citation>
-<Title>Identification of catalytic nucleophile of Escherichia coli gamma-glutamyltranspeptidase by gamma-monofluorophosphono derivative of glutamic acid: N-terminal thr-391 in small subunit is the nucleophile.</Title>
-<Xref>DOI:10.1021/bi000220p</Xref>
-<Xref>PMID:10869181</Xref>
-<Note>mass-spectrometric analysis of chemically labeled active site; Fig. 6 sequence should read TTHYSVVDK which matches the translation and the masses</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Okada, T.</Author>
-<Author>Suzuki, H.</Author>
-<Author>Wada, K.</Author>
-<Author>Kumagai, H.</Author>
-<Author>Fukuyama, K.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 103, 6471-6476, 2006</Citation>
-<Title>Crystal structures of gamma-glutamyltranspeptidase from Escherichia coli, a key enzyme in glutathione metabolism, and its reaction intermediate.</Title>
-<Xref>DOI:10.1073/pnas.0511020103</Xref>
-<Xref>PMID:16618936</Xref>
-<Note>the active site threonine of gamma-glutamyltranspeptidase forms a gamma-glutamyl ester intermediate</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Okada, T.</Author>
-<Author>Wada, K.</Author>
-<Author>Fukuyama, K.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, December 2005</Citation>
-<Description>Crystal structure of gamma-glutamyltranspeptidase from Escherichia coli acyl-enzyme intermediate.</Description>
-<Xref>PDB:2DBW</Xref>
-<Note>X-ray diffraction, 1.80 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Abdul Ajees, A.</Author>
-<Author>Gunasekaran, K.</Author>
-<Author>Volanakis, J.E.</Author>
-<Author>Narayana, S.V.</Author>
-<Author>Kotwal, G.J.</Author>
-<Author>Murthy, H.M.</Author>
-</Authors>
-<Citation>Nature 444, 221-225, 2006</Citation>
-<Title>The structure of complement C3b provides insights into complement activation and regulation.</Title>
-<Xref>DOI:10.1038/nature05258</Xref>
-<Xref>PMID:17051152</Xref>
-<Note>X-ray diffraction, 2.26 angstroms; N-acetyl-L-threonine is the model substrate</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Abdul Ajees, A.</Author>
-<Author>Gunasekaran, K.</Author>
-<Author>Volanakis, J.E.</Author>
-<Author>Narayana, S.V.</Author>
-<Author>Kotwal, G.J.</Author>
-<Author>Murthy, H.M.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, July 2006</Citation>
-<Description>Structure of complement C3B: Insights into complement activation and regulation.</Description>
-<Xref>PDB:2HR0</Xref>
-<Note>X-ray diffraction, 2.26 angstroms; N-acetyl-L-threonine is the model substrate; Caution: structures from the laboratory of H.M. Murthy have been withdrawn at the request of the University of Alabama, and although this report has been questioned, it has not been withdrwan</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Janssen, B.J.</Author>
-<Author>Read, R.J.</Author>
-<Author>Brünger, A.T.</Author>
-<Author>Gros, P.</Author>
-</Authors>
-<Citation>Nature 448, E1-2; discussion E2-E1-2; discussion E3, 2007</Citation>
-<Title>Crystallography: crystallographic evidence for deviating C3b structure.</Title>
-<Xref>DOI:10.1038/nature06102</Xref>
-<Xref>PMID:17687277</Xref>
-<Note>report of inconsistencies among structures</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Wada, K.</Author>
-<Author>Hiratake, J.</Author>
-<Author>Irie, M.</Author>
-<Author>Okada, T.</Author>
-<Author>Yamada, C.</Author>
-<Author>Kumagai, H.</Author>
-<Author>Suzuki, H.</Author>
-<Author>Fukuyama, K.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 380, 361-372, 2008</Citation>
-<Title>Crystal structures of Escherichia coli gamma-glutamyltranspeptidase in complex with azaserine and acivicin: novel mechanistic implication for inhibition by glutamine antagonists.</Title>
-<Xref>DOI:10.1016/j.jmb.2008.05.007</Xref>
-<Xref>PMID:18555071</Xref>
-<Note>X-ray diffraction, 1.65 angstroms</Note>
-</ReferenceBlock>
-<Comment>The formula and records labeled "TQX" refers to O3-(isoglutamyl)threonine produced as an ester cross-link of a peptidyl threonine residue and a peptidyl glutamic acid residue. The ester cross-link between threonine residues of target proteins and complement C3 and C4 glutamine residues occurs autocatalytically after C3 and C4 form internal intermediate thioester cross-links with the liberation of ammonia.</Comment>
-<Comment>The formula and records labeled "THR" refers to O3-(isoglutamyl)threonine produced as a peptidyl threonine residue ester bonded to a free glutamine with the release of ammonia. The isoglutamylation modification of threonine by glutamine is predicted to be produced by autocatalysis as an intermediate in the catalytic cycle of glutaminases that are homologous to asparaginase.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode link="THR">
-<SequenceSpec>T</SequenceSpec>
-<Xref>PSI-MOD:01785</Xref>
-</SequenceCode>
-<SequenceCode link="TQX">
-<SequenceSpec>Q, T</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:01952</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0536.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0536.PDB" />
-</Entry>
-<Entry id="AA0537">
-<Header>
-<Code>AA0537</Code>
-<Dates>
-<CreationDate>30-Sep-2010</CreationDate>
-<StrucRevDate>30-Sep-2010</StrucRevDate>
-<TextChngDate>29-Oct-2010</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>3'-nitro-L-tyrosine</Name>
-<AlternateName>3-nitro-L-tyrosine</AlternateName>
-<AlternateName>3-nitrotyrosine</AlternateName>
-<AlternateName>m-nitrotyrosine</AlternateName>
-<AlternateName>meta-nitrotyrosine</AlternateName>
-<SystematicName>(2S)-2-amino-3-(4-hydroxy-3-nitrophenyl)propanoic acid</SystematicName>
-<Xref>CAS:3604-79-3</Xref>
-<Xref>CAS:621-44-3</Xref>
-<Xref>ChEBI:44454</Xref>
-<Xref>PDBHET:NIY</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 8 N 2 O 4</Formula>
-<Weight type="chemical">208.17</Weight>
-<Weight type="physical">208.048407</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0019">
-<Formula>C 0 H -1 N 1 O 2</Formula>
-<Weight type="chemical">45.00</Weight>
-<Weight type="physical">44.985078</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lyashenko, A.V.</Author>
-<Author>Bento, I.</Author>
-<Author>Zaitsev, V.N.</Author>
-<Author>Zhukhlistova, N.E.</Author>
-<Author>Zhukova, Y.N.</Author>
-<Author>Gabdoulkhakov, A.G.</Author>
-<Author>Morgunova, E.Y.</Author>
-<Author>Voelter, W.</Author>
-<Author>Kachalova, G.S.</Author>
-<Author>Stepanova, E.V.</Author>
-<Author>Koroleva, O.V.</Author>
-<Author>Lamzin, V.S.</Author>
-<Author>Tishkov, V.I.</Author>
-<Author>Betzel, C.</Author>
-<Author>Lindley, P.F.</Author>
-<Author>Mikhailov, A.M.</Author>
-</Authors>
-<Citation>J. Biol. Inorg. Chem. 11, 963-973, 2006</Citation>
-<Title>X-ray structural studies of the fungal laccase from Cerrena maxima.</Title>
-<Xref>DOI:10.1007/s00775-006-0158-x</Xref>
-<Xref>PMID:16944230</Xref>
-<Note>X-ray diffraction, 1.9 angstroms; the sequence was modeled by homology; the protein was not artifactually exposed to peroxynitrite; no chemical evidence was obtained for this modification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lyashenko, A.V.</Author>
-<Author>Zhukova, Y.N.</Author>
-<Author>Mikhailov, A.M.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, June 2008</Citation>
-<Description>Crystal structure studies of laccase from Cerrena maxima at 1.76 A resolution.</Description>
-<Xref>PDB:3DIV</Xref>
-<Note>X-ray diffraction, 1.76 angstroms</Note>
-</ReferenceBlock>
-<Comment>This modification is produced artifactually by treatment with peroxynitrite.</Comment>
-<SequenceCode>
-<SequenceSpec>Y</SequenceSpec>
-<Xref>PSI-MOD:01786</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="mod_res__3'-nitrotyrosine__y">MOD_RES 3'-Nitrotyrosine</Feature>
-</Features>
-<Image src="/images/AA0537.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0537.PDB" />
-</Entry>
-<Entry id="AA0538">
-<Header>
-<Code>AA0538</Code>
-<Dates>
-<CreationDate>29-Oct-2010</CreationDate>
-<StrucRevDate>29-Oct-2010</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N,N-dimethyl-L-leucine</Name>
-<AlternateName>2-(dimethylamino)-4-methylvaleric acid</AlternateName>
-<AlternateName>2-(dimethylazanyl)-4-methylpentanoic acid</AlternateName>
-<AlternateName>N,N-dimethylleucine</AlternateName>
-<SystematicName>(2S)-2-(dimethylamino)-4-methylpentanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 8 H 16 N 1 O 1</Formula>
-<Weight type="chemical">142.22</Weight>
-<Weight type="physical">142.123189</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0011">
-<Formula>C 2 H 4 N 0 O 0</Formula>
-<Weight type="chemical">28.05</Weight>
-<Weight type="physical">28.031300</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Armirotti, A.</Author>
-<Author>Damonte, G.</Author>
-<Author>Pozzolini, M.</Author>
-<Author>Mussino, F.</Author>
-<Author>Cerrano, C.</Author>
-<Author>Salis, A.</Author>
-<Author>Benatti, U.</Author>
-<Author>Giovine, M.</Author>
-</Authors>
-<Citation>J. Proteome Res. 8, 3995-4004, 2009</Citation>
-<Title>Primary structure and post-translational modifications of silicatein beta from the marine sponge Petrosia ficiformis (Poiret, 1789).</Title>
-<Xref>DOI:10.1021/pr900342y</Xref>
-<Xref>PMID:19522542</Xref>
-<Note>mass spectrometric identification; the authors do not provide numeric data to support their mass-spectrometric interpretations</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>protein N-terminal methyltransferase (EC 2.1.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>L</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>PSI-MOD:01806</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-<Keyword>methylated amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n,n-dimethylleucine__l">MOD_RES N,N-dimethylleucine</Feature>
-</Features>
-<Image src="/images/AA0538.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0538.PDB" />
-</Entry>
-<Entry id="AA0539">
-<Header>
-<Code>AA0539</Code>
-<Dates>
-<CreationDate>29-Oct-2010</CreationDate>
-<StrucRevDate>29-Oct-2010</StrucRevDate>
-<TextChngDate>31-Mar-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-formyl-L-glutamic acid</Name>
-<AlternateName>2-(formylazanyl)pentanedioic acid</AlternateName>
-<AlternateName>2-formamidopentanedioic acid</AlternateName>
-<AlternateName>2-formylaminopentanedioic acid</AlternateName>
-<SystematicName>(2S)-2-(formylamino)pentanedioic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 8 N 1 O 4</Formula>
-<Weight type="chemical">158.13</Weight>
-<Weight type="physical">158.045333</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0006">
-<Formula>C 1 H 0 N 0 O 1</Formula>
-<Weight type="chemical">28.01</Weight>
-<Weight type="physical">27.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Shen, P.-T.</Author>
-<Author>Hsu, J.-L.</Author>
-<Author>Chen, S.-H.</Author>
-</Authors>
-<Citation>Anal. Chem. 79, 9520-9530, 2007</Citation>
-<Title>Dimethyl isotope-coded affinity selection for the analysis of free and blocked N-termini of proteins using LC-MS/MS.</Title>
-<Xref>DOI:10.1021/ac701678h</Xref>
-<Xref>PMID:18001127</Xref>
-<Note>it is extremely improbable that the source tissue MCF-7, a mammary tumor cell line, produces a processed immunoglobulin, and the enzymatic origin of the modification in that tissue is not explained; authors' initials in the PubMed citation are corrected</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>E</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>PSI-MOD:01807</Xref>
-</SequenceCode>
-<Source>deprecated</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-<Keyword>formylation</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this dubious modification is not currently annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0539.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0539.PDB" />
-</Entry>
-<Entry id="AA0540">
-<Header>
-<Code>AA0540</Code>
-<Dates>
-<CreationDate>29-Nov-2010</CreationDate>
-<StrucRevDate>29-Nov-2010</StrucRevDate>
-<TextChngDate>30-Sep-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-cysteine 3-hydroxy-2,5-pyridinedicarboxylic acid</Name>
-<AlternateName>6-[1-azanyl-2-sulfanylethyl]-3-hydroxypyridine-2,5-dicarboxylic acid</AlternateName>
-<SystematicName>6-[(1R)-1-amino-2-sulfanylethyl]-3-hydroxypyridine-2,5-dicarboxylic acid</SystematicName>
-<Xref>PDBHET:MH6</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 7 N 2 O 3 S 1</Formula>
-<Weight type="chemical">223.23</Weight>
-<Weight type="physical">223.017738</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0016 AA0016">
-<Formula>C 0 H -8 N -1 O -2 S 0</Formula>
-<Weight type="chemical">-54.07</Weight>
-<Weight type="physical">-54.055504</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Pascard, C.</Author>
-<Author>Ducruix, A.</Author>
-<Author>Lunel, J.</Author>
-<Author>Prangé, T.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 99, 6418-6423, 1977</Citation>
-<Title>Highly modified cysteine-containing antibiotics. Chemical structure and configuration of nosiheptide.</Title>
-<Xref>DOI:10.1021/ja00461a039</Xref>
-<Xref>PMID:893891</Xref>
-<Note>X-ray diffraction; the resolution is not specified; the structure is deposited in the Cambridge Structural Database entry NOSHEP10</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Harms, J.M.</Author>
-<Author>Wilson, D.N.</Author>
-<Author>Schluenzen, F.</Author>
-<Author>Connell, S.R.</Author>
-<Author>Stachelhaus, T.</Author>
-<Author>Zaborowska, Z.</Author>
-<Author>Spahn, C.M.</Author>
-<Author>Fucini, P.</Author>
-</Authors>
-<Citation>Mol. Cell 30, 26-38, 2008</Citation>
-<Title>Translational regulation via L11: molecular switches on the ribosome turned on and off by thiostrepton and micrococcin.</Title>
-<Xref>DOI:10.1016/j.molcel.2008.01.009</Xref>
-<Xref>PMID:18406324</Xref>
-<Note>X-ray diffraction, 2.50 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Harms, J.M.</Author>
-<Author>Wilson, D.N.</Author>
-<Author>Schluenzen, F.</Author>
-<Author>Connell, S.R.</Author>
-<Author>Stachelhaus, T.</Author>
-<Author>Zaborowska, Z.</Author>
-<Author>Spahn, C.M.</Author>
-<Author>Fucini, P.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, March 2008</Citation>
-<Description>Thiopeptide antibiotic nosiheptide bound to the large ribosomal subunit of Deinococcus radiodurans.</Description>
-<Xref>PDB:2ZJP</Xref>
-<Note>X-ray diffraction, 3.70 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yu, Y.</Author>
-<Author>Duan, L.</Author>
-<Author>Zhang, Q.</Author>
-<Author>Liao, R.</Author>
-<Author>Ding, Y.</Author>
-<Author>Pan, H.</Author>
-<Author>Wendt-Pienkowski, E.</Author>
-<Author>Tang, G.</Author>
-<Author>Shen, B.</Author>
-<Author>Liu, W.</Author>
-</Authors>
-<Citation>ACS Chem. Biol. 4, 855-864, 2009</Citation>
-<Title>Nosiheptide biosynthesis featuring a unique indole side ring formation on the characteristic thiopeptide framework.</Title>
-<Xref>DOI:10.1021/cb900133x</Xref>
-<Xref>PMID:19678698</Xref>
-</ReferenceBlock>
-<Comment>Formed by the metathesis of two didehydroalanines made from serines, condensation with a cysteine carbonyl and dehydrogenation.</Comment>
-<Comment>This modification is currently represented in the PDB as part of the HET group for the entire molecule of nosiheptide.</Comment>
-<SequenceCode>
-<SequenceSpec>C, S, S</SequenceSpec>
-<Condition>cross-link 3</Condition>
-<Condition>incidental to RESID:AA0244</Condition>
-<Xref>PSI-MOD:01814</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>pyridine ring</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__3-hydroxypyridine-2,5-dicarboxylic acid (ser-ser) (with c-__s__s">CROSSLNK 3-hydroxypyridine-2,5-dicarboxylic acid (Ser-Ser) (with C-...)</Feature>
-<Feature type="UniProt" key="crosslnk__3-hydroxypyridine-2,5-dicarboxylic acid (ser-cys) (with s-__s__c">CROSSLNK 3-hydroxypyridine-2,5-dicarboxylic acid (Ser-Cys) (with S-...)</Feature>
-</Features>
-<Image src="/images/AA0540.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0540.PDB" />
-</Entry>
-<Entry id="AA0541">
-<Header>
-<Code>AA0541</Code>
-<Dates>
-<CreationDate>29-Nov-2010</CreationDate>
-<StrucRevDate>29-Nov-2010</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-glutamate thiazole-4-carboxylic acid</Name>
-<AlternateName>2-[-1-azanyl-3-carboxypropyl]-1,3-thiazole-4-carboxylic acid</AlternateName>
-<SystematicName>2-[(1S)-1-amino-3-carboxypropyl]-1,3-thiazole-4-carboxylic acid</SystematicName>
-<Xref>PDBHET:BB9</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 8 H 8 N 2 O 3 S 1</Formula>
-<Weight type="chemical">212.22</Weight>
-<Weight type="physical">212.025563</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0006">
-<Formula>C 0 H -4 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-20.03</Weight>
-<Weight type="physical">-20.026215</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Pascard, C.</Author>
-<Author>Ducruix, A.</Author>
-<Author>Lunel, J.</Author>
-<Author>Prangé, T.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 99, 6418-6423, 1977</Citation>
-<Title>Highly modified cysteine-containing antibiotics. Chemical structure and configuration of nosiheptide.</Title>
-<Xref>DOI:10.1021/ja00461a039</Xref>
-<Xref>PMID:893891</Xref>
-<Note>X-ray diffraction</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Harms, J.M.</Author>
-<Author>Wilson, D.N.</Author>
-<Author>Schluenzen, F.</Author>
-<Author>Connell, S.R.</Author>
-<Author>Stachelhaus, T.</Author>
-<Author>Zaborowska, Z.</Author>
-<Author>Spahn, C.M.</Author>
-<Author>Fucini, P.</Author>
-</Authors>
-<Citation>Mol. Cell 30, 26-38, 2008</Citation>
-<Title>Translational regulation via L11: molecular switches on the ribosome turned on and off by thiostrepton and micrococcin.</Title>
-<Xref>DOI:10.1016/j.molcel.2008.01.009</Xref>
-<Xref>PMID:18406324</Xref>
-<Note>X-ray diffraction, 2.50 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Harms, J.M.</Author>
-<Author>Wilson, D.N.</Author>
-<Author>Schluenzen, F.</Author>
-<Author>Connell, S.R.</Author>
-<Author>Stachelhaus, T.</Author>
-<Author>Zaborowska, Z.</Author>
-<Author>Spahn, C.M.</Author>
-<Author>Fucini, P.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, March 2008</Citation>
-<Description>Thiopeptide antibiotic nosiheptide bound to the large ribosomal subunit of Deinococcus radiodurans.</Description>
-<Xref>PDB:2ZJP</Xref>
-<Note>X-ray diffraction, 3.70 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yu, Y.</Author>
-<Author>Duan, L.</Author>
-<Author>Zhang, Q.</Author>
-<Author>Liao, R.</Author>
-<Author>Ding, Y.</Author>
-<Author>Pan, H.</Author>
-<Author>Wendt-Pienkowski, E.</Author>
-<Author>Tang, G.</Author>
-<Author>Shen, B.</Author>
-<Author>Liu, W.</Author>
-</Authors>
-<Citation>ACS Chem. Biol. 4, 855-864, 2009</Citation>
-<Title>Nosiheptide biosynthesis featuring a unique indole side ring formation on the characteristic thiopeptide framework.</Title>
-<Xref>DOI:10.1021/cb900133x</Xref>
-<Xref>PMID:19678698</Xref>
-</ReferenceBlock>
-<Comment>Formed by the condensation of a cysteine thiol with the carbonyl of the preceding residue and alpha-beta dehydrogenation.</Comment>
-<Comment>This modification is currently represented in the PDB as part of the HET group for the entire molecule of nosiheptide.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptidyl-cysteine cyclase (EC 4.2.1.-)</EnzymeName>
-<EnzymeName>peptidyl-thiazoline dehydrogenase (EC 1.3.-.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C, E</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Condition>incidental to RESID:AA0487</Condition>
-<Condition>incidental to RESID:AA0488</Condition>
-<Xref>PSI-MOD:01815</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>oxazole/thiazole ring</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__thiazole-4-carboxylic acid (glu-cys)__e__c">CROSSLNK Thiazole-4-carboxylic acid (Glu-Cys)</Feature>
-</Features>
-<Image src="/images/AA0541.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0541.PDB" />
-</Entry>
-<Entry id="AA0542">
-<Header>
-<Code>AA0542</Code>
-<Dates>
-<CreationDate>31-Dec-2010</CreationDate>
-<StrucRevDate>31-Dec-2010</StrucRevDate>
-<TextChngDate>25-Feb-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>2'-hydroxy-L-tryptophan</Name>
-<AlternateName>2-azanyl-3-(2-hydroxy-1H-indol-3-yl)propanoic acid</AlternateName>
-<AlternateName>2-hydroxy-L-tryptophan</AlternateName>
-<AlternateName>2-hydroxy-tryptophan</AlternateName>
-<SystematicName>(2S)-2-amino-3-(2-hydroxy-1H-indol-3-yl)propanoic acid</SystematicName>
-<Xref>PDBHET:TRO</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 11 H 10 N 2 O 2</Formula>
-<Weight type="chemical">202.21</Weight>
-<Weight type="physical">202.074228</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0018">
-<Formula>C 0 H 0 N 0 O 1</Formula>
-<Weight type="chemical">16.00</Weight>
-<Weight type="physical">15.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Oubrie, A.</Author>
-<Author>Rozeboom, H.J.</Author>
-<Author>Kalk, K.H.</Author>
-<Author>Huizinga, E.G.</Author>
-<Author>Dijkstra, B.W.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 277, 3727-3732, 2002</Citation>
-<Title>Crystal structure of quinohemoprotein alcohol dehydrogenase from Comamonas testosteroni: structural basis for substrate oxidation and electron transfer.</Title>
-<Xref>DOI:10.1074/jbc.M109403200</Xref>
-<Xref>PMID:11714714</Xref>
-<Note>X-ray diffraction, 1.44 angstroms; the modification is not discussed in the paper</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Rozeboom, H.J.</Author>
-<Author>Oubrie, A.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, November 2001</Citation>
-<Description>Crystal structure of quinohemoprotein alcohol dehydrogenase from Comamonas testosteroni.</Description>
-<Xref>PDB:1KB0</Xref>
-<Note>X-ray diffraction, 1.44 angstroms; in the PDB entry the modification is assigned the HET group TRO and called 2-hydroxy-tryptophan; both CG and CD1 are trigonal planar</Note>
-</ReferenceBlock>
-<Comment>This modification may be produced artifactually.</Comment>
-<SequenceCode>
-<SequenceSpec>W</SequenceSpec>
-<Xref>PSI-MOD:01816</Xref>
-</SequenceCode>
-<Source>artifactual</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0542.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0542.PDB" />
-</Entry>
-<Entry id="AA0543">
-<Header>
-<Code>AA0543</Code>
-<Dates>
-<CreationDate>31-Dec-2010</CreationDate>
-<StrucRevDate>31-Dec-2010</StrucRevDate>
-<TextChngDate>25-Feb-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>2'-oxo-L-tryptophan</Name>
-<AlternateName>2-azanyl-3-[(3S)-2-oxo-2,3-dihydro-1H-indol-3-yl]propanoic acid</AlternateName>
-<AlternateName>2-oxo-L-tryptophan</AlternateName>
-<AlternateName>2-oxotryptophan</AlternateName>
-<SystematicName>(2S)-2-amino-3-[(3S)-2-oxo-2,3-dihydro-1H-indol-3-yl]propanoic acid</SystematicName>
-<Xref>PDBHET:TRO</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 11 H 10 N 2 O 2</Formula>
-<Weight type="chemical">202.21</Weight>
-<Weight type="physical">202.074228</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0018">
-<Formula>C 0 H 0 N 0 O 1</Formula>
-<Weight type="chemical">16.00</Weight>
-<Weight type="physical">15.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lubkowski, J.</Author>
-<Author>Hennecke, F.</Author>
-<Author>Plückthun, A.</Author>
-<Author>Wlodawer, A.</Author>
-</Authors>
-<Citation>Nature Struct. Biol. 5, 140-147, 1998</Citation>
-<Title>The structural basis of phage display elucidated by the crystal structure of the N-terminal domains of g3p.</Title>
-<Xref>DOI:10.1038/nsb0298-140</Xref>
-<Xref>PMID:9461080</Xref>
-<Note>X-ray diffraction, 1.46 angstroms; the authors model the modification as 2'-oxotryptophan with CD1 trigonal planar and CG tetrahedral; the modification is not chemically characterized</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lubkowski, J.</Author>
-<Author>Hennecke, F.</Author>
-<Author>Pluckthun, A.</Author>
-<Author>Wlodawer, A.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, December 1997</Citation>
-<Description>Crystal structure of the N-terminal domains of bacteriophage minor coat protein G3P.</Description>
-<Xref>PDB:1G3P</Xref>
-<Note>X-ray diffraction, 1.46 angstroms; in the PDB entry the modification is assigned the HET group TRO and called 2-hydroxy-tryptophan</Note>
-</ReferenceBlock>
-<Comment>This modification, which is not observed in other preparations of the same protein, is probably produced artifactually.</Comment>
-<SequenceCode>
-<SequenceSpec>W</SequenceSpec>
-<Xref>PSI-MOD:01817</Xref>
-</SequenceCode>
-<Source>artifactual</Source>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0543.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0543.PDB" />
-</Entry>
-<Entry id="AA0544">
-<Header>
-<Code>AA0544</Code>
-<Dates>
-<CreationDate>31-Dec-2010</CreationDate>
-<StrucRevDate>31-Dec-2010</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>1-(L-tryptophan-3-yl)-L-tryptophan</Name>
-<AlternateName>(2S,2'S)-3,3'-(3'H-1,3'-biindole-3,3'-diyl)bis(2-aminopropanoic acid)</AlternateName>
-<AlternateName>2-amino-3-[2-[2-amino-3-(2-carboxyethyl)-1H-indol-4-yl]-1H-indol-3-yl]propanoic acid</AlternateName>
-<AlternateName>3-[2-azanyl-2-carboxyethyl]-3-(3-[2-azanyl-2-carboxyethyl]-1H-indol-2-yl)-1H-indole</AlternateName>
-<AlternateName>ditryptophan</AlternateName>
-<SystematicName>3-[(2S)-2-amino-2-carboxyethyl]-3-(3-[(2S)-2-amino-2-carboxyethyl]-1H-indol-2-yl)-1H-indole</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 22 H 18 N 4 O 2</Formula>
-<Weight type="chemical">370.41</Weight>
-<Weight type="physical">370.142976</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0018 AA0018">
-<Formula>C 0 H -2 N 0 O 0</Formula>
-<Weight type="chemical">-2.02</Weight>
-<Weight type="physical">-2.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Medinas, D.B.</Author>
-<Author>Gozzo, F.C.</Author>
-<Author>Santos, L.F.</Author>
-<Author>Iglesias, A.H.</Author>
-<Author>Augusto, O.</Author>
-</Authors>
-<Citation>Free Radic. Biol. Med. 49, 1046-1053, 2010</Citation>
-<Title>A ditryptophan cross-link is responsible for the covalent dimerization of human superoxide dismutase 1 during its bicarbonate-dependent peroxidase activity.</Title>
-<Xref>DOI:10.1016/j.freeradbiomed.2010.06.018</Xref>
-<Xref>PMID:20600836</Xref>
-<Note>mass spectrometric and linkage analysis</Note>
-</ReferenceBlock>
-<Comment>The production of this cross-link during bicarbonate-dependent peroxidase catalysis may be artifactual.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>W, W</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:01818</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="crosslnk__1-(tryptophan-3-yl)-tryptophan (trp-trp)__w__w">CROSSLNK 1-(tryptophan-3-yl)-tryptophan (Trp-Trp)</Feature>
-</Features>
-<Image src="/images/AA0544.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0544.PDB" />
-</Entry>
-<Entry id="AA0545">
-<Header>
-<Code>AA0545</Code>
-<Dates>
-<CreationDate>31-Dec-2010</CreationDate>
-<StrucRevDate>31-Dec-2010</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6-succinyl-L-lysine</Name>
-<AlternateName>2-azanyl-6-[(3-carboxypropanoyl)azanyl]hexanoic acid</AlternateName>
-<AlternateName>4-[[(5S)-5-amino-6-hydroxy-6-oxohexyl]amino]-4-oxobutanoate</AlternateName>
-<AlternateName>N(epsilon)-(succinyl)lysine</AlternateName>
-<AlternateName>succinyllysine</AlternateName>
-<SystematicName>(2S)-2-amino-6-[(3-carboxypropanoyl)amino]hexanoic acid</SystematicName>
-<Xref>CAS:52685-16-2</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 10 H 16 N 2 O 4</Formula>
-<Weight type="chemical">228.25</Weight>
-<Weight type="physical">228.111007</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 4 H 4 N 0 O 3</Formula>
-<Weight type="chemical">100.07</Weight>
-<Weight type="physical">100.016044</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Platt, T.</Author>
-<Author>Files, J.G.</Author>
-<Author>Weber, K.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 248, 110-121, 1973</Citation>
-<Title>Lac repressor. Specific proteolytic destruction of the NH2-terminal region and loss of the deoxyribonucleic acid-binding activity.</Title>
-<Xref>PMID:4571224</Xref>
-<Note>chemical synthesis and chromatographic detection</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Dimick, S.M.</Author>
-<Author>Powell, S.C.</Author>
-<Author>McMahon, S.A.</Author>
-<Author>Moothoo D.N.</Author>
-<Author>Naismith, J.H.</Author>
-<Author>Toone, E.J.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 121, 10286-10296, 1999</Citation>
-<Title>On the Meaning of Affinity: Cluster Glycoside Effects and Concanavalin A.</Title>
-<Xref>DOI:10.1021/ja991729e</Xref>
-<Note>X-ray diffraction, 2.66 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Naismith, J.H.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, April 1999</Citation>
-<Description>Room temperature structure of concanavalin A complexed to bivalent ligand.</Description>
-<Xref>PDB:1QGL</Xref>
-<Note>X-ray diffraction, 2.66 angstroms; each subunit of a homodimer contains one succinylated lysine, but the modification can be resolved only in one subunit, and the distance from NZ to C1 is 4.44 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kawai, Y.</Author>
-<Author>Fujii, H.</Author>
-<Author>Okada, M.</Author>
-<Author>Tsuchie, Y.</Author>
-<Author>Uchida, K.</Author>
-<Author>Osawa, T.</Author>
-</Authors>
-<Citation>J. Lipid Res. 47, 1386-1398, 2006</Citation>
-<Title>Formation of Nepsilon-(succinyl)lysine in vivo: a novel marker for docosahexaenoic acid-derived protein modification.</Title>
-<Xref>DOI:10.1194/jlr.M600091-JLR200</Xref>
-<Xref>PMID:16582421</Xref>
-<Note>chromatographic detection; mass spectrometric identification; a major product after radical-catalyzed peroxidation of docosahexaenoic acid</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Zhang, Z.</Author>
-<Author>Tan, M.</Author>
-<Author>Xie, Z.</Author>
-<Author>Dai, L.</Author>
-<Author>Chen, Y.</Author>
-<Author>Zhao, Y.</Author>
-</Authors>
-<Citation>Nature Chem. Biol. 7, 58-63, 2011</Citation>
-<Title>Identification of lysine succinylation as a new post-translational modification.</Title>
-<Xref>DOI:10.1038/nchembio.495</Xref>
-<Xref>PMID:21151122</Xref>
-<Note>mass spectrometric detection; chromatographic and radiolabeling identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Du, J.</Author>
-<Author>Zhou, Y.</Author>
-<Author>Su, X.</Author>
-<Author>Yu, J.J.</Author>
-<Author>Khan, S.</Author>
-<Author>Jiang, H.</Author>
-<Author>Kim, J.</Author>
-<Author>Woo, J.</Author>
-<Author>Kim, J.H.</Author>
-<Author>Choi, B.H.</Author>
-<Author>He, B.</Author>
-<Author>Chen, W.</Author>
-<Author>Zhang, S.</Author>
-<Author>Cerione, R.A.</Author>
-<Author>Auwerx, J.</Author>
-<Author>Hao, Q.</Author>
-<Author>Lin, H.</Author>
-</Authors>
-<Citation>Science 334, 806-809, 2011</Citation>
-<Title>Sirt5 is a NAD-dependent protein lysine demalonylase and desuccinylase.</Title>
-<Xref>DOI:10.1126/science.1207861</Xref>
-<Xref>PMID:22076378</Xref>
-<Note>mass spectrometric identification in a number of mitochondrial proteins; identification of Sirt5 as a desuccinylase and increase of detectable succinylation of carbamoyl phosphate synthase 1 when Sirt5 is deleted</Note>
-</ReferenceBlock>
-<Comment>The responsible generating enzyme activity is not identified. This modification can be reversed by Sirt5.</Comment>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>PSI-MOD:01819</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="mod_res__n6-succinyllysine__k">MOD_RES N6-succinyllysine</Feature>
-</Features>
-<Image src="/images/AA0545.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0545.PDB" />
-</Entry>
-<Entry id="AA0546">
-<Header>
-<Code>AA0546</Code>
-<Dates>
-<CreationDate>25-Feb-2011</CreationDate>
-<StrucRevDate>25-Feb-2011</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-allo-isoleucine</Name>
-<AlternateName>2-azanyl-3-methylpentanoic acid</AlternateName>
-<AlternateName>3-methyl-norvaline</AlternateName>
-<AlternateName>allo-L-isoleucine</AlternateName>
-<AlternateName>alpha-amino-beta-methylvaleric acid</AlternateName>
-<AlternateName>L-threo-isoleucine</AlternateName>
-<SystematicName>(2S,3R)-2-amino-3-methylpentanoic acid</SystematicName>
-<Xref>CAS:1509-34-8</Xref>
-<Xref>ChEBI:30008</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 11 N 1 O 1</Formula>
-<Weight type="chemical">113.16</Weight>
-<Weight type="physical">113.084064</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0010">
-<Formula>C 0 H 0 N 0 O 0</Formula>
-<Weight type="chemical">0.00</Weight>
-<Weight type="physical">0.000000</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Minami, Y.</Author>
-<Author>Yoshida, K.</Author>
-<Author>Azuma, R.</Author>
-<Author>Urakawa, A.</Author>
-<Author>Kawauchi, T.</Author>
-<Author>Otani, T.</Author>
-<Author>Komiyama, K.</Author>
-<Author>Omura, S.</Author>
-</Authors>
-<Citation>Tetrahedron Lett. 35, 8001-8004, 1994</Citation>
-<Title>Structure of cypemycin, a new peptide antibiotic.</Title>
-<Xref>DOI:10.1016/0040-4039(94)80033-2</Xref>
-<Note>mass spectrometric, (1)H-NMR, and (13)C-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Claesen, J.</Author>
-<Author>Bibb, M.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 107, 16297-16302, 2010</Citation>
-<Title>Genome mining and genetic analysis of cypemycin biosynthesis reveal an unusual class of posttranslationally modified peptides.</Title>
-<Xref>DOI:10.1073/pnas.1008608107</Xref>
-<Xref>PMID:20805503</Xref>
-<Note>gene sequence for the encoded peptide, biosynthesis</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>protein-isoleucine 3-epimerase (EC 5.1.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>I</SequenceSpec>
-<Xref>PSI-MOD:01840</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="mod_res__l-allo-isoleucine__i">MOD_RES L-allo-isoleucine</Feature>
-</Features>
-<Image src="/images/AA0546.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0546.PDB" />
-</Entry>
-<Entry id="AA0547">
-<Header>
-<Code>AA0547</Code>
-<Dates>
-<CreationDate>25-Feb-2011</CreationDate>
-<StrucRevDate>25-Feb-2011</StrucRevDate>
-<TextChngDate>20-May-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>(E)-dehydrobutyrine</Name>
-<AlternateName>(E)-2-amino-2-butenoic acid</AlternateName>
-<AlternateName>(E)-2-aminobutenoic acid</AlternateName>
-<AlternateName>2,3-didehydrobutyrine</AlternateName>
-<AlternateName>3-methyldehydroalanine</AlternateName>
-<AlternateName>alpha,beta-dehydroaminobutyric acid</AlternateName>
-<AlternateName>anhydrothreonine</AlternateName>
-<AlternateName>Dhb</AlternateName>
-<AlternateName>methyl-dehydroalanine</AlternateName>
-<SystematicName>(2E)-2-aminobut-2-enoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 5 N 1 O 1</Formula>
-<Weight type="chemical">83.09</Weight>
-<Weight type="physical">83.037114</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0017">
-<Formula>C 0 H -2 N 0 O -1</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Piard, J.C.</Author>
-<Author>Kuipers, O.P.</Author>
-<Author>Rollema, H.S.</Author>
-<Author>Desmazeaud, M.J.</Author>
-<Author>de Vos, W.M.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 268, 16361-16368, 1993</Citation>
-<Title>Structure, organization, and expression of the lct gene for lacticin 481, a novel lantibiotic produced by Lactococcus lactis.</Title>
-<Xref>PMID:8344922</Xref>
-<Note>the E- and Z- isomers are distinguished by (1)H-NOE NMR</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Minami, Y.</Author>
-<Author>Yoshida, K.</Author>
-<Author>Azuma, R.</Author>
-<Author>Urakawa, A.</Author>
-<Author>Kawauchi, T.</Author>
-<Author>Otani, T.</Author>
-<Author>Komiyama, K.</Author>
-<Author>Omura, S.</Author>
-</Authors>
-<Citation>Tetrahedron Lett. 35, 8001-8004, 1994</Citation>
-<Title>Structure of cypemycin, a new peptide antibiotic.</Title>
-<Xref>DOI:10.1016/0040-4039(94)80033-2</Xref>
-<Note>mass spectrometric, (1)H-NMR, and (13)C-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Claesen, J.</Author>
-<Author>Bibb, M.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 107, 16297-16302, 2010</Citation>
-<Title>Genome mining and genetic analysis of cypemycin biosynthesis reveal an unusual class of posttranslationally modified peptides.</Title>
-<Xref>DOI:10.1073/pnas.1008608107</Xref>
-<Xref>PMID:20805503</Xref>
-<Note>gene sequence for the encoded peptide, biosynthesis</Note>
-</ReferenceBlock>
-<Comment>In some cases it has not been firmly established whether the natural form is the Z or the E isomer. For the Z isomer, see RESID:AA0182.</Comment>
-<Comment>A 2,3-didehydro amino acid blocks Edman degradation.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>protein-threonine dehydratase (EC 4.2.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>T</SequenceSpec>
-<Xref>PSI-MOD:00190</Xref>
-<Xref>PSI-MOD:01470</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="mod_res__(e)-2,3-didehydrobutyrine__t">MOD_RES (E)-2,3-didehydrobutyrine</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="mod_res__2,3-didehydrobutyrine__t">MOD_RES 2,3-didehydrobutyrine</Feature>
-<Note>this UniProt feature is used when the stereochemistry has not been determined</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0547.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0547.PDB" />
-</Entry>
-<Entry id="AA0548">
-<Header>
-<Code>AA0548</Code>
-<Dates>
-<CreationDate>25-Feb-2011</CreationDate>
-<StrucRevDate>25-Feb-2011</StrucRevDate>
-<TextChngDate>20-May-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-(2-aminovinyl)-L-cysteine</Name>
-<AlternateName>(R,Z)-S-(2-aminovinyl)cysteine</AlternateName>
-<SystematicName>(2R)-2-amino-3-([(Z)-2-aminoethenyl]sulfanyl)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 7 N 2 O 1 S 1</Formula>
-<Weight type="chemical">143.18</Weight>
-<Weight type="physical">143.027909</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005">
-<Formula>C -1 H -4 N 0 O -2 S -1</Formula>
-<Weight type="chemical">-80.10</Weight>
-<Weight type="physical">-79.993200</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Minami, Y.</Author>
-<Author>Yoshida, K.</Author>
-<Author>Azuma, R.</Author>
-<Author>Urakawa, A.</Author>
-<Author>Kawauchi, T.</Author>
-<Author>Otani, T.</Author>
-<Author>Komiyama, K.</Author>
-<Author>Omura, S.</Author>
-</Authors>
-<Citation>Tetrahedron Lett. 35, 8001-8004, 1994</Citation>
-<Title>Structure of cypemycin, a new peptide antibiotic.</Title>
-<Xref>DOI:10.1016/0040-4039(94)80033-2</Xref>
-<Note>mass spectrometric, (1)H-NMR, and (13)C-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Claesen, J.</Author>
-<Author>Bibb, M.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 107, 16297-16302, 2010</Citation>
-<Title>Genome mining and genetic analysis of cypemycin biosynthesis reveal an unusual class of posttranslationally modified peptides.</Title>
-<Xref>DOI:10.1073/pnas.1008608107</Xref>
-<Xref>PMID:20805503</Xref>
-<Note>gene sequence for the encoded peptide, biosynthesis; the authors did not have enough material to determine the stereochemistry and assume that it was the D stereoisomer [private communication]</Note>
-</ReferenceBlock>
-<Comment>This cross-link arises from the decarboxylation of the carboxyl-terminal portion of a lanthionine, either L-lanthionine (see RESID:AA0110) or meso-lanthionine (see RESID:AA0111).</Comment>
-<Comment>The stereochemistry of the (2-aminovinyl)-cysteine in cypemycin has not been determined. For the D stereoisomer, see RESID:AA0204.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptidyl-cysteine dethiolase (EC 4.4.1.-)</EnzymeName>
-<EnzymeName>peptidyl-cysteine dehydroalanine/dehydrobutyrine ligase (EC 6.2.-.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C, C</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:01842</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>lanthionine</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0548.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0548.PDB" />
-</Entry>
-<Entry id="AA0549">
-<Header>
-<Code>AA0549</Code>
-<Dates>
-<CreationDate>25-Feb-2011</CreationDate>
-<StrucRevDate>25-Feb-2011</StrucRevDate>
-<TextChngDate>25-Feb-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>5'-chloro-L-tryptophan</Name>
-<SystematicName>(2S)-2-amino-3-(5-chloro-1H-indol-3-yl)propanoic acid</SystematicName>
-<Xref>CAS:33468-35-8</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 11 Cl 1 H 9 N 2 O 1</Formula>
-<Weight type="chemical">220.66</Weight>
-<Weight type="physical">220.040341</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0018">
-<Formula>C 0 Cl 1 H -1 N 0 O 0</Formula>
-<Weight type="chemical">34.44</Weight>
-<Weight type="physical">33.961028</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Castiglione, F.</Author>
-<Author>Lazzarini, A.</Author>
-<Author>Carrano, L.</Author>
-<Author>Corti, E.</Author>
-<Author>Ciciliato, I.</Author>
-<Author>Gastaldo, L.</Author>
-<Author>Candiani, P.</Author>
-<Author>Losi, D.</Author>
-<Author>Marinelli, F.</Author>
-<Author>Selva, E.</Author>
-<Author>Parenti, F.</Author>
-</Authors>
-<Citation>Chem. Biol. 15, 22-31, 2008</Citation>
-<Title>Determining the structure and mode of action of microbisporicin, a potent lantibiotic active against multiresistant pathogens.</Title>
-<Xref>DOI:10.1016/j.chembiol.2007.11.009</Xref>
-<Xref>PMID:18215770</Xref>
-<Note>mass spectrometric, (1)H-NMR, and (13)C-NMR identification</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>W</SequenceSpec>
-<Xref>PSI-MOD:01843</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>chlorine</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__5'-chlorotryptophan__w">MOD_RES 5'-chlorotryptophan</Feature>
-</Features>
-<Image src="/images/AA0549.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0549.PDB" />
-</Entry>
-<Entry id="AA0550">
-<Header>
-<Code>AA0550</Code>
-<Dates>
-<CreationDate>31-Mar-2011</CreationDate>
-<StrucRevDate>31-Mar-2011</StrucRevDate>
-<TextChngDate>28-Oct-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>2-(3-methylbutanoyl)-5-hydroxyoxazole-4-carbothionic acid</Name>
-<AlternateName>(4Z)-4-[hydroxy(sulfanyl)methylidene]-2-(3-methylbutanoyl)-1,3-oxazol-5(4H)-one [tautomer]</AlternateName>
-<SystematicName>5-hydroxy-2-(3-methylbutanoyl)-1,3-oxazole-4-carbothioic O-acid</SystematicName>
-<Xref>PDBHET:8LI</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 10 N 1 O 3 S 1</Formula>
-<Weight type="chemical">212.24</Weight>
-<Weight type="physical">212.038139</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0011">
-<Formula>C 0 H -7 N -1 O 1 S 0</Formula>
-<Weight type="chemical">-5.06</Weight>
-<Weight type="physical">-5.062935</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kim, H.J.</Author>
-<Author>Graham, D.W.</Author>
-<Author>DiSpirito, A.A.</Author>
-<Author>Alterman, M.A.</Author>
-<Author>Galeva, N.</Author>
-<Author>Larive, C.K.</Author>
-<Author>Asunskis, D.</Author>
-<Author>Sherwood, P.M.</Author>
-</Authors>
-<Citation>Science 305, 1612-1615, 2004</Citation>
-<Title>Methanobactin, a copper-acquisition compound from methane-oxidizing bacteria.</Title>
-<Xref>DOI:10.1126/science.1098322</Xref>
-<Xref>PMID:15361623</Xref>
-<Note>mass spectrometric and chemical characterization; X-ray diffraction, 1.5 angstroms; proposed structure in Cambridge Crystallographic Data Center (241254)</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Behling, L.A.</Author>
-<Author>Hartsel, S.C.</Author>
-<Author>Lewis, D.E.</Author>
-<Author>DiSpirito, A.A.</Author>
-<Author>Choi, D.W.</Author>
-<Author>Masterson, L.R.</Author>
-<Author>Veglia, G.</Author>
-<Author>Gallagher, W.H.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 130, 12604-12605, 2008</Citation>
-<Title>NMR, mass spectrometry and chemical evidence reveal a different chemical structure for methanobactin that contains oxazolone rings.</Title>
-<Xref>DOI:10.1021/ja804747d</Xref>
-<Xref>PMID:18729522</Xref>
-<Note>(1)H-NMR, (13)C-NMR and (15)N-NMR identification; structure revision</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Krentz, B.D.</Author>
-<Author>Mulheron, H.J.</Author>
-<Author>Semrau, J.D.</Author>
-<Author>Dispirito, A.A.</Author>
-<Author>Bandow, N.L.</Author>
-<Author>Haft, D.H.</Author>
-<Author>Vuilleumier, S.</Author>
-<Author>Murrell, J.C.</Author>
-<Author>McEllistrem, M.T.</Author>
-<Author>Hartsel, S.C.</Author>
-<Author>Gallagher, W.H.</Author>
-</Authors>
-<Citation>Biochemistry 49, 10117-10130, 2010</Citation>
-<Title>A comparison of methanobactins from Methylosinus trichosporium OB3b and Methylocystis strain Sb2 predicts methanobactins are synthesized from diverse peptide precursors modified to create a common core for binding and reducing copper ions.</Title>
-<Xref>DOI:10.1021/bi1014375</Xref>
-<Xref>PMID:20961038</Xref>
-<Note>(1)H-NMR, (13)C-NMR and (15)N-NMR identification; structure revision; gene sequence for the encoded peptide</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>El Ghazouani, A.</Author>
-<Author>Baslé, A.</Author>
-<Author>Firbank, S.J.</Author>
-<Author>Knapp, C.W.</Author>
-<Author>Gray, J.</Author>
-<Author>Graham, D.W.</Author>
-<Author>Dennison, C.</Author>
-</Authors>
-<Citation>Inorg. Chem. 50, 1378-1391, 2011</Citation>
-<Title>Copper-Binding Properties and Structures of Methanobactins from Methylosinus trichosporium OB3b.</Title>
-<Xref>DOI:10.1021/ic101965j</Xref>
-<Xref>PMID:21254756</Xref>
-<Note>X-ray diffraction, 0.92 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>El Ghazouani, A.</Author>
-<Author>Basle, A.</Author>
-<Author>Firbank, S.J.</Author>
-<Author>Knapp, C.W.</Author>
-<Author>Gray, J.</Author>
-<Author>Graham, D.W.</Author>
-<Author>Dennison, C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, July 2010</Citation>
-<Description>Structures and copper-binding properties of methanobactins from Methylosinus trichosporium OB3b.</Description>
-<Xref>PDB:2XJH</Xref>
-<Note>X-ray diffraction, 2.50 angstroms</Note>
-</ReferenceBlock>
-<Comment>The amino group of the following amino acid forms a thiopeptide bond. The amino(sulfanyl)methylidene tautomeric form is shown in the diagram and model.</Comment>
-<Comment>The biosynthesis of this modification from the encoded cysteine peptide has not been elaborated.</Comment>
-<SequenceCode>
-<SequenceSpec> C, L</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Condition>cross-link 1</Condition>
-<Xref>PSI-MOD:01844</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>imidazolinone/oxazolinone ring</Keyword>
-<Keyword>thiopeptide bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__2-(3-methylbutanoyl)-5-hydroxyoxazole-4-carbothionic acid (leu-cys)__l__c">MOD_RES 2-(3-methylbutanoyl)-5-hydroxyoxazole-4-carbothionic acid (Leu-Cys)</Feature>
-</Features>
-<Image src="/images/AA0550.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0550.PDB" />
-</Entry>
-<Entry id="AA0551">
-<Header>
-<Code>AA0551</Code>
-<Dates>
-<CreationDate>31-Mar-2011</CreationDate>
-<StrucRevDate>31-Mar-2011</StrucRevDate>
-<TextChngDate>28-Oct-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-proline 5-hydroxy-oxazole-4-carbothionic acid</Name>
-<AlternateName>(4Z)-4-[hydroxy(sulfanyl)methylidene]-2-[(2S)-pyrrolidin-2-yl]-1,3-oxazol-5(4H)-one [tautomer]</AlternateName>
-<SystematicName>5-hydroxy-2-[(2S)-pyrrolidin-2-yl]-1,3-oxazole-4-carbothioic O-acid</SystematicName>
-<Xref>PDBHET:66G</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 8 H 8 N 2 O 2 S 1</Formula>
-<Weight type="chemical">196.22</Weight>
-<Weight type="physical">196.030649</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0015">
-<Formula>C 0 H -4 N 0 O 0 S 0</Formula>
-<Weight type="chemical">-4.03</Weight>
-<Weight type="physical">-4.031300</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kim, H.J.</Author>
-<Author>Graham, D.W.</Author>
-<Author>DiSpirito, A.A.</Author>
-<Author>Alterman, M.A.</Author>
-<Author>Galeva, N.</Author>
-<Author>Larive, C.K.</Author>
-<Author>Asunskis, D.</Author>
-<Author>Sherwood, P.M.</Author>
-</Authors>
-<Citation>Science 305, 1612-1615, 2004</Citation>
-<Title>Methanobactin, a copper-acquisition compound from methane-oxidizing bacteria.</Title>
-<Xref>DOI:10.1126/science.1098322</Xref>
-<Xref>PMID:15361623</Xref>
-<Note>mass spectrometric and chemical characterization; X-ray diffraction, 1.5 angstroms; proposed structure in Cambridge Crystallographic Data Center (241254)</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Behling, L.A.</Author>
-<Author>Hartsel, S.C.</Author>
-<Author>Lewis, D.E.</Author>
-<Author>DiSpirito, A.A.</Author>
-<Author>Choi, D.W.</Author>
-<Author>Masterson, L.R.</Author>
-<Author>Veglia, G.</Author>
-<Author>Gallagher, W.H.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 130, 12604-12605, 2008</Citation>
-<Title>NMR, mass spectrometry and chemical evidence reveal a different chemical structure for methanobactin that contains oxazolone rings.</Title>
-<Xref>DOI:10.1021/ja804747d</Xref>
-<Xref>PMID:18729522</Xref>
-<Note>(1)H-NMR, (13)C-NMR and (15)N-NMR identification; structure revision</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Krentz, B.D.</Author>
-<Author>Mulheron, H.J.</Author>
-<Author>Semrau, J.D.</Author>
-<Author>Dispirito, A.A.</Author>
-<Author>Bandow, N.L.</Author>
-<Author>Haft, D.H.</Author>
-<Author>Vuilleumier, S.</Author>
-<Author>Murrell, J.C.</Author>
-<Author>McEllistrem, M.T.</Author>
-<Author>Hartsel, S.C.</Author>
-<Author>Gallagher, W.H.</Author>
-</Authors>
-<Citation>Biochemistry 49, 10117-10130, 2010</Citation>
-<Title>A comparison of methanobactins from Methylosinus trichosporium OB3b and Methylocystis strain Sb2 predicts methanobactins are synthesized from diverse peptide precursors modified to create a common core for binding and reducing copper ions.</Title>
-<Xref>DOI:10.1021/bi1014375</Xref>
-<Xref>PMID:20961038</Xref>
-<Note>(1)H-NMR, (13)C-NMR and (15)N-NMR identification; structure revision; gene sequence for the encoded peptide</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>El Ghazouani, A.</Author>
-<Author>Baslé, A.</Author>
-<Author>Firbank, S.J.</Author>
-<Author>Knapp, C.W.</Author>
-<Author>Gray, J.</Author>
-<Author>Graham, D.W.</Author>
-<Author>Dennison, C.</Author>
-</Authors>
-<Citation>Inorg. Chem. 50, 1378-1391, 2011</Citation>
-<Title>Copper-Binding Properties and Structures of Methanobactins from Methylosinus trichosporium OB3b.</Title>
-<Xref>DOI:10.1021/ic101965j</Xref>
-<Xref>PMID:21254756</Xref>
-<Note>X-ray diffraction, 0.92 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>El Ghazouani, A.</Author>
-<Author>Basle, A.</Author>
-<Author>Firbank, S.J.</Author>
-<Author>Knapp, C.W.</Author>
-<Author>Gray, J.</Author>
-<Author>Graham, D.W.</Author>
-<Author>Dennison, C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, July 2010</Citation>
-<Description>Structures and copper-binding properties of methanobactins from Methylosinus trichosporium OB3b.</Description>
-<Xref>PDB:2XJH</Xref>
-<Note>X-ray diffraction, 2.50 angstroms</Note>
-</ReferenceBlock>
-<Comment>The amino group of the following amino acid forms a thiopeptide bond. The amino(sulfanyl)methylidene tautomeric form is shown in the diagram and model.</Comment>
-<Comment>The biosynthesis of this modification from the encoded cysteine peptide has not been elaborated.</Comment>
-<SequenceCode>
-<SequenceSpec> C, P</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Xref>PSI-MOD:01845</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>imidazolinone/oxazolinone ring</Keyword>
-<Keyword>thiopeptide bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__proline 5-hydroxy-oxazole-4-carbothionic acid (pro-cys)__p__c">CROSSLNK Proline 5-hydroxy-oxazole-4-carbothionic acid (Pro-Cys)</Feature>
-</Features>
-<Image src="/images/AA0551.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0551.PDB" />
-</Entry>
-<Entry id="AA0552">
-<Header>
-<Code>AA0552</Code>
-<Dates>
-<CreationDate>31-Mar-2011</CreationDate>
-<StrucRevDate>28-Oct-2011</StrucRevDate>
-<TextChngDate>28-Oct-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>methanobactin OB3b copper complex</Name>
-<SystematicName>bis[4-(hydroxy[sulfanyl-kappaS]methylidene)-1,3-oxazol-5(4H)-onato-kappaN]copper</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 6 Cu 1 H 0 N 2 O 4 S 2</Formula>
-<Weight type="chemical">291.74</Weight>
-<Weight type="physical">290.859546</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005">
-<Formula>C 0 Cu 1 H -10 N 0 O 2 S 0</Formula>
-<Weight type="chemical">85.46</Weight>
-<Weight type="physical">84.841176</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kim, H.J.</Author>
-<Author>Graham, D.W.</Author>
-<Author>DiSpirito, A.A.</Author>
-<Author>Alterman, M.A.</Author>
-<Author>Galeva, N.</Author>
-<Author>Larive, C.K.</Author>
-<Author>Asunskis, D.</Author>
-<Author>Sherwood, P.M.</Author>
-</Authors>
-<Citation>Science 305, 1612-1615, 2004</Citation>
-<Title>Methanobactin, a copper-acquisition compound from methane-oxidizing bacteria.</Title>
-<Xref>DOI:10.1126/science.1098322</Xref>
-<Xref>PMID:15361623</Xref>
-<Note>mass spectrometric and chemical characterization; X-ray diffraction, 1.5 angstroms; proposed structure in Cambridge Crystallographic Data Center (241254)</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Behling, L.A.</Author>
-<Author>Hartsel, S.C.</Author>
-<Author>Lewis, D.E.</Author>
-<Author>DiSpirito, A.A.</Author>
-<Author>Choi, D.W.</Author>
-<Author>Masterson, L.R.</Author>
-<Author>Veglia, G.</Author>
-<Author>Gallagher, W.H.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 130, 12604-12605, 2008</Citation>
-<Title>NMR, mass spectrometry and chemical evidence reveal a different chemical structure for methanobactin that contains oxazolone rings.</Title>
-<Xref>DOI:10.1021/ja804747d</Xref>
-<Xref>PMID:18729522</Xref>
-<Note>(1)H-NMR, (13)C-NMR and (15)N-NMR identification; structure revision</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Krentz, B.D.</Author>
-<Author>Mulheron, H.J.</Author>
-<Author>Semrau, J.D.</Author>
-<Author>Dispirito, A.A.</Author>
-<Author>Bandow, N.L.</Author>
-<Author>Haft, D.H.</Author>
-<Author>Vuilleumier, S.</Author>
-<Author>Murrell, J.C.</Author>
-<Author>McEllistrem, M.T.</Author>
-<Author>Hartsel, S.C.</Author>
-<Author>Gallagher, W.H.</Author>
-</Authors>
-<Citation>Biochemistry 49, 10117-10130, 2010</Citation>
-<Title>A comparison of methanobactins from Methylosinus trichosporium OB3b and Methylocystis strain Sb2 predicts methanobactins are synthesized from diverse peptide precursors modified to create a common core for binding and reducing copper ions.</Title>
-<Xref>DOI:10.1021/bi1014375</Xref>
-<Xref>PMID:20961038</Xref>
-<Note>(1)H-NMR, (13)C-NMR and (15)N-NMR identification; structure revision; gene sequence for the encoded peptide</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>El Ghazouani, A.</Author>
-<Author>Baslé, A.</Author>
-<Author>Firbank, S.J.</Author>
-<Author>Knapp, C.W.</Author>
-<Author>Gray, J.</Author>
-<Author>Graham, D.W.</Author>
-<Author>Dennison, C.</Author>
-</Authors>
-<Citation>Inorg. Chem. 50, 1378-1391, 2011</Citation>
-<Title>Copper-Binding Properties and Structures of Methanobactins from Methylosinus trichosporium OB3b.</Title>
-<Xref>DOI:10.1021/ic101965j</Xref>
-<Xref>PMID:21254756</Xref>
-<Note>X-ray diffraction, 0.92 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>El Ghazouani, A.</Author>
-<Author>Basle, A.</Author>
-<Author>Firbank, S.J.</Author>
-<Author>Knapp, C.W.</Author>
-<Author>Gray, J.</Author>
-<Author>Graham, D.W.</Author>
-<Author>Dennison, C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, July 2010</Citation>
-<Description>Structures and copper-binding properties of methanobactins from Methylosinus trichosporium OB3b.</Description>
-<Xref>PDB:2XJH</Xref>
-<Note>X-ray diffraction, 2.50 angstroms</Note>
-</ReferenceBlock>
-<Comment>This entry represents the copper binding portions of methanobactin OB3b, which are derived from cysteine residues. The modification of these cysteines, which has not been experimentally elaborated, includes crosslinking with the carboxyl group of residue N-1 to form 1,3-oxazol-5-one rings, and formation of a thiopeptide bond with the amino group of residue N+1.</Comment>
-<Comment>The modified residue N-1 is presented in a separate entry and is not included in the mass accounting of this entry. The original carboxyl atom of residue N-1, and the hydroxyl lost from thionic acid in forming the thiopeptide are shown in gray in the diagram.</Comment>
-<SequenceCode>
-<SequenceSpec> C, C</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Condition>secondary to RESID:AA0550</Condition>
-<Condition>secondary to RESID:AA0551</Condition>
-<Xref>PSI-MOD:01846</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>copper</Keyword>
-<Keyword>metalloprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="metal__copper [cu-methanobactin ob3b complex]__c">METAL copper [Cu-methanobactin OB3b complex]</Feature>
-</Features>
-<Image src="/images/AA0552.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0552.PDB" />
-</Entry>
-<Entry id="AA0553">
-<Header>
-<Code>AA0553</Code>
-<Dates>
-<CreationDate>30-Jun-2011</CreationDate>
-<StrucRevDate>30-Jun-2011</StrucRevDate>
-<TextChngDate>28-Oct-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>2-(4-guanidinobutanoyl)-5-hydroxyimidazole-4-carbothionic acid</Name>
-<AlternateName>(4Z)-2-(4-guanidinobutanoyl)-5-oxo-4-(sulfanylmethylidene)-4,5-dihydro-1H-imidazole</AlternateName>
-<AlternateName>2-(4-guanidinobutanoyl)-5-hydroxy-4-thioformyl-1H-imidazole [tautomer]</AlternateName>
-<SystematicName>2-(4-guanidinobutanoyl)-5-hydroxy-1H-imidazole-4-carbothioic O-acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 12 N 5 O 2 S 1</Formula>
-<Weight type="chemical">254.29</Weight>
-<Weight type="physical">254.071171</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0002 AA0005">
-<Formula>C 0 H -6 N 0 O 0 S 0</Formula>
-<Weight type="chemical">-6.05</Weight>
-<Weight type="physical">-6.046950</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Krentz, B.D.</Author>
-<Author>Mulheron, H.J.</Author>
-<Author>Semrau, J.D.</Author>
-<Author>Dispirito, A.A.</Author>
-<Author>Bandow, N.L.</Author>
-<Author>Haft, D.H.</Author>
-<Author>Vuilleumier, S.</Author>
-<Author>Murrell, J.C.</Author>
-<Author>McEllistrem, M.T.</Author>
-<Author>Hartsel, S.C.</Author>
-<Author>Gallagher, W.H.</Author>
-</Authors>
-<Citation>Biochemistry 49, 10117-10130, 2010</Citation>
-<Title>A comparison of methanobactins from Methylosinus trichosporium OB3b and Methylocystis strain Sb2 predicts methanobactins are synthesized from diverse peptide precursors modified to create a common core for binding and reducing copper ions.</Title>
-<Xref>DOI:10.1021/bi1014375</Xref>
-<Xref>PMID:20961038</Xref>
-<Note>(1)H-NMR, (13)C-NMR and (15)N-NMR identification</Note>
-</ReferenceBlock>
-<Comment>The amino group of the following amino acid forms a thiopeptide bond. This is an amino(sulfanyl)methylidene in the tautomeric form, which is shown in the diagram and model.</Comment>
-<SequenceCode>
-<SequenceSpec>C, R</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Condition>cross-link 1</Condition>
-<Xref>PSI-MOD:01877</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>imidazolinone/oxazolinone ring</Keyword>
-<Keyword>thiopeptide bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__2-(4-guanidinobutanoyl)-5-hydroxyimidazole-4-carbothionic acid (arg-cys)__r__c">CROSSLNK 2-(4-guanidinobutanoyl)-5-hydroxyimidazole-4-carbothionic acid (Arg-Cys)</Feature>
-</Features>
-<Image src="/images/AA0553.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0553.PDB" />
-</Entry>
-<Entry id="AA0554">
-<Header>
-<Code>AA0554</Code>
-<Dates>
-<CreationDate>30-Jun-2011</CreationDate>
-<StrucRevDate>30-Jun-2011</StrucRevDate>
-<TextChngDate>28-Oct-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-threonine 5-hydroxy-oxazole-4-carbonthionic acid</Name>
-<AlternateName>(4Z)-2-[(1S,2R)-1-amino-2-hydroxypropyl]-4-(sulfanylmethylidene)-1,3-oxazol-5(4H)-one [tautomer]</AlternateName>
-<SystematicName>2-[(1S,2R)-1-amino-2-hydroxypropyl]-5-hydroxy-1,3-oxazole-4-carbothioic O-acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 8 N 2 O 3 S 1</Formula>
-<Weight type="chemical">200.21</Weight>
-<Weight type="physical">200.025563</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0017">
-<Formula>C 0 H -4 N 0 O 0 S 0</Formula>
-<Weight type="chemical">-4.03</Weight>
-<Weight type="physical">-4.031300</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Krentz, B.D.</Author>
-<Author>Mulheron, H.J.</Author>
-<Author>Semrau, J.D.</Author>
-<Author>Dispirito, A.A.</Author>
-<Author>Bandow, N.L.</Author>
-<Author>Haft, D.H.</Author>
-<Author>Vuilleumier, S.</Author>
-<Author>Murrell, J.C.</Author>
-<Author>McEllistrem, M.T.</Author>
-<Author>Hartsel, S.C.</Author>
-<Author>Gallagher, W.H.</Author>
-</Authors>
-<Citation>Biochemistry 49, 10117-10130, 2010</Citation>
-<Title>A comparison of methanobactins from Methylosinus trichosporium OB3b and Methylocystis strain Sb2 predicts methanobactins are synthesized from diverse peptide precursors modified to create a common core for binding and reducing copper ions.</Title>
-<Xref>DOI:10.1021/bi1014375</Xref>
-<Xref>PMID:20961038</Xref>
-<Note>(1)H-NMR, (13)C-NMR and (15)N-NMR identification</Note>
-</ReferenceBlock>
-<Comment>The amino group of the following amino acid forms a thiopeptide bond. This is an amino(sulfanyl)methylidene in the tautomeric form, which is shown in the diagram and model.</Comment>
-<SequenceCode>
-<SequenceSpec>C, T</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Xref>PSI-MOD:01878</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>imidazolinone/oxazolinone ring</Keyword>
-<Keyword>thiopeptide bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__threonine 5-hydroxy-oxazole-4-carbonthionic acid (thr-cys)__t__c">CROSSLNK Threonine 5-hydroxy-oxazole-4-carbonthionic acid (Thr-Cys)</Feature>
-</Features>
-<Image src="/images/AA0554.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0554.PDB" />
-</Entry>
-<Entry id="AA0555">
-<Header>
-<Code>AA0555</Code>
-<Dates>
-<CreationDate>30-Jun-2011</CreationDate>
-<StrucRevDate>28-Oct-2011</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>methanobactin SB2 copper complex</Name>
-<SystematicName>[5-(hydroxy[sulfanyl-kappaS]methylene)-3,5-dihydro-4H-imidazol-4-onato-kappaN1][4-(hydroxy[sulfanyl-kappaS]methylene)-1,3-oxazol-5(4H)-onato-kappaN]copper</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 6 Cu 1 H 1 N 3 O 3 S 2</Formula>
-<Weight type="chemical">290.76</Weight>
-<Weight type="physical">289.875530</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005">
-<Formula>C 0 Cu 1 H -9 N 1 O 1 S 0</Formula>
-<Weight type="chemical">84.48</Weight>
-<Weight type="physical">83.857161</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Krentz, B.D.</Author>
-<Author>Mulheron, H.J.</Author>
-<Author>Semrau, J.D.</Author>
-<Author>Dispirito, A.A.</Author>
-<Author>Bandow, N.L.</Author>
-<Author>Haft, D.H.</Author>
-<Author>Vuilleumier, S.</Author>
-<Author>Murrell, J.C.</Author>
-<Author>McEllistrem, M.T.</Author>
-<Author>Hartsel, S.C.</Author>
-<Author>Gallagher, W.H.</Author>
-</Authors>
-<Citation>Biochemistry 49, 10117-10130, 2010</Citation>
-<Title>A comparison of methanobactins from Methylosinus trichosporium OB3b and Methylocystis strain Sb2 predicts methanobactins are synthesized from diverse peptide precursors modified to create a common core for binding and reducing copper ions.</Title>
-<Xref>DOI:10.1021/bi1014375</Xref>
-<Xref>PMID:20961038</Xref>
-<Note>(1)H-NMR, (13)C-NMR and (15)N-NMR identification</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>C, C</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Condition>secondary to RESID:AA0553</Condition>
-<Condition>secondary to RESID:AA0554</Condition>
-<Xref>PSI-MOD:01879</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>copper</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="metal__copper [cu-methanobactin sb2 complex]__c">METAL copper [Cu-methanobactin SB2 complex]</Feature>
-</Features>
-<Image src="/images/AA0555.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0555.PDB" />
-</Entry>
-<Entry id="AA0556">
-<Header>
-<Code>AA0556</Code>
-<Dates>
-<CreationDate>31-Mar-2011</CreationDate>
-<StrucRevDate>31-Mar-2011</StrucRevDate>
-<TextChngDate>31-Mar-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-cysteine sulfonic acid</Name>
-<AlternateName>2-amino-2-carboxyethanesulfonic acid</AlternateName>
-<AlternateName>2-azanyl-3-sulfopropanoic acid</AlternateName>
-<AlternateName>3-sulfoalanine</AlternateName>
-<AlternateName>cysteic acid</AlternateName>
-<AlternateName>cysteine sulphonic acid</AlternateName>
-<SystematicName>(2R)-2-amino-3-sulfopropanoic acid</SystematicName>
-<Xref>CAS:498-40-8</Xref>
-<Xref>ChEBI:17285</Xref>
-<Xref>PDBHET:OCS</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 5 N 1 O 4 S 1</Formula>
-<Weight type="chemical">151.14</Weight>
-<Weight type="physical">150.993929</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 0 H 0 N 0 O 3 S 0</Formula>
-<Weight type="chemical">48.00</Weight>
-<Weight type="physical">47.984744</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Armirotti, A.</Author>
-<Author>Damonte, G.</Author>
-<Author>Pozzolini, M.</Author>
-<Author>Mussino, F.</Author>
-<Author>Cerrano, C.</Author>
-<Author>Salis, A.</Author>
-<Author>Benatti, U.</Author>
-<Author>Giovine, M.</Author>
-</Authors>
-<Citation>J. Proteome Res. 8, 3995-4004, 2009</Citation>
-<Title>Primary structure and post-translational modifications of silicatein beta from the marine sponge Petrosia ficiformis (Poiret, 1789).</Title>
-<Xref>DOI:10.1021/pr900342y</Xref>
-<Xref>PMID:19522542</Xref>
-<Note>mass spectrometric identification after treatment with sulfuric/nitric acid (4:1), and ammonium fluoride and hydrofluoric acid; the authors do not provide numeric data to support their mass-spectrometric interpretations</Note>
-</ReferenceBlock>
-<Comment>This modification is easily produced artifactually. Cysteine sulfinic acid (see RESID:AA0262) exposed to air oxidizes to cysteic acid.</Comment>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>PSI-MOD:00460</Xref>
-</SequenceCode>
-<Source>artifactual</Source>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this dubious modification is not currently annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0556.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0556.PDB" />
-</Entry>
-<Entry id="AA0557">
-<Header>
-<Code>AA0557</Code>
-<Dates>
-<CreationDate>31-Mar-2011</CreationDate>
-<StrucRevDate>31-Mar-2011</StrucRevDate>
-<TextChngDate>31-Mar-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-cysteine sulfinyl phosphate</Name>
-<AlternateName>cysteine sulfinic phosphoryl ester</AlternateName>
-<SystematicName>(2R)-2-amino-3-[(phosphonooxy)sulfinyl]propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 3 H 6 N 1 O 6 P 1 S 1</Formula>
-<Weight type="chemical">215.12</Weight>
-<Weight type="physical">214.965345</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 0 H 1 N 0 O 5 P 1 S 0</Formula>
-<Weight type="chemical">111.98</Weight>
-<Weight type="physical">111.956160</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Jeong, W.</Author>
-<Author>Park, S.J.</Author>
-<Author>Chang, T.S.</Author>
-<Author>Lee, D.Y.</Author>
-<Author>Rhee, S.G.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 281, 14400-14407, 2006</Citation>
-<Title>Molecular mechanism of the reduction of cysteine sulfinic acid of peroxiredoxin to cysteine by mammalian sulfiredoxin.</Title>
-<Xref>DOI:10.1074/jbc.M511082200</Xref>
-<Xref>PMID:16565085</Xref>
-</ReferenceBlock>
-<Comment>This modification is probably produced as an intermediate during the ATP mediated reduction of cysteine sulfinic acid (see RESID:AA0262) formed in some proteins during oxidative stress.</Comment>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>PSI-MOD:01847</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0557.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0557.PDB" />
-</Entry>
-<Entry id="AA0558">
-<Header>
-<Code>AA0558</Code>
-<Dates>
-<CreationDate>31-Mar-2011</CreationDate>
-<StrucRevDate>31-Mar-2011</StrucRevDate>
-<TextChngDate>20-May-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-(spermidinoglutathion-S-yl)-L-cysteine</Name>
-<AlternateName>cysteine glutathionylspermidine disulfide</AlternateName>
-<AlternateName>L-gamma-glutamyl-[S-(L-cystein-S-yl)]-L-cysteinyl-N-{3-[(4-aminobutyl)amino]propyl}glycinamide</AlternateName>
-<SystematicName>(2R)-2-amino-3-([(2R)-2-([(4S)-4-amino-4-carboxybutanoyl]amino)-2-([2-([3-([4-aminobutyl]amino)propyl]carbamoyl)methyl]carbamoyl)ethyl]disulfanyl)propanoic acid</SystematicName>
-<Xref>CAS:33932-35-3</Xref>
-<Xref>ChEBI:16613</Xref>
-<Xref>PDBHET:TS5</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 20 H 37 N 7 O 6 S 2</Formula>
-<Weight type="chemical">535.68</Weight>
-<Weight type="physical">535.224674</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 17 H 32 N 6 O 5 S 1</Formula>
-<Weight type="chemical">432.54</Weight>
-<Weight type="physical">432.215489</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Chiang, B.Y.</Author>
-<Author>Chen, T.C.</Author>
-<Author>Pai, C.H.</Author>
-<Author>Chou, C.C.</Author>
-<Author>Chen, H.H.</Author>
-<Author>Ko, T.P.</Author>
-<Author>Hsu, W.H.</Author>
-<Author>Chang, C.Y.</Author>
-<Author>Wu, W.F.</Author>
-<Author>Wang, A.H.</Author>
-<Author>Lin, C.H.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 285, 25345-25353, 2010</Citation>
-<Title>Protein S-thiolation by Glutathionylspermidine (Gsp): the role of Escherichia coli Gsp synthetASE/amidase in redox regulation.</Title>
-<Xref>DOI:10.1074/jbc.M110.133363</Xref>
-<Xref>PMID:20530482</Xref>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hofmann, B.</Author>
-<Author>Budde, H.</Author>
-<Author>Bruns, K.</Author>
-<Author>Guerrero, S.A.</Author>
-<Author>Kalisz, H.M.</Author>
-<Author>Menge, U.</Author>
-<Author>Montemartini, M.</Author>
-<Author>Nogoceke, E.</Author>
-<Author>Steinert, P.</Author>
-<Author>Wissing, J.B.</Author>
-<Author>Flohé, L.</Author>
-<Author>Hecht, H.J.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 382, 459-471, 2001</Citation>
-<Title>Structures of tryparedoxins revealing interaction with trypanothione.</Title>
-<Xref>DOI:10.1515/BC.2001.056</Xref>
-<Xref>PMID:11347894</Xref>
-<Note>X-ray diffraction, 1.40 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hofmann, B.</Author>
-<Author>Budde, H.</Author>
-<Author>Bruns, K.</Author>
-<Author>Guerrero, S.A.</Author>
-<Author>Kalisz, H.M.</Author>
-<Author>Menge, U.</Author>
-<Author>Montemartini, M.</Author>
-<Author>Nogoceke, E.</Author>
-<Author>Steinert, P.</Author>
-<Author>Wissing, J.B.</Author>
-<Author>Flohe, L.</Author>
-<Author>Hecht, H.J.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, February 2001</Citation>
-<Description>Tryparedoxin II complexed with glutathionylspermidine.</Description>
-<Xref>PDB:1I5G</Xref>
-<Note>X-ray diffraction, 1.40 angstroms</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>PSI-MOD:01848</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>disulfide bond</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0558.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0558.PDB" />
-</Entry>
-<Entry id="AA0559">
-<Header>
-<Code>AA0559</Code>
-<Dates>
-<CreationDate>20-May-2011</CreationDate>
-<StrucRevDate>20-May-2011</StrucRevDate>
-<TextChngDate>24-Aug-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>2-(L-cystein-S-yl)-methionine</Name>
-<SystematicName>(2R)-2-amino-2-([2-amino-2-carboxyethyl]sulfanyl)-4-(methylsulfanyl)butanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 8 H 12 N 2 O 2 S 2</Formula>
-<Weight type="chemical">232.32</Weight>
-<Weight type="physical">232.034020</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0013">
-<Formula>C 0 H -2 N 0 O 0 S 0</Formula>
-<Weight type="chemical">-2.02</Weight>
-<Weight type="physical">-2.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Liu, W.T.</Author>
-<Author>Yang, Y.L.</Author>
-<Author>Xu, Y.</Author>
-<Author>Lamsa, A.</Author>
-<Author>Haste, N.M.</Author>
-<Author>Yang, J.Y.</Author>
-<Author>Ng, J.</Author>
-<Author>Gonzalez, D.</Author>
-<Author>Ellermeier, C.D.</Author>
-<Author>Straight, P.D.</Author>
-<Author>Pevzner, P.A.</Author>
-<Author>Pogliano, J.</Author>
-<Author>Nizet, V.</Author>
-<Author>Pogliano, K.</Author>
-<Author>Dorrestein, P.C.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 107, 16286-16290, 2010</Citation>
-<Title>Imaging mass spectrometry of intraspecies metabolic exchange revealed the cannibalistic factors of Bacillus subtilis.</Title>
-<Xref>DOI:10.1073/pnas.1008368107</Xref>
-<Xref>PMID:20805502</Xref>
-<Note>mass spectrometric and (1)H-NMR identification; the sterochemistry was not determined</Note>
-</ReferenceBlock>
-<Comment>The stereochemistry of the methionine alpha-carbon has not been determined. The R form is shown.</Comment>
-<SequenceCode>
-<SequenceSpec>C, M</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:01857</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__2-(s-cysteinyl)-methionine (cys-met)__c__m">CROSSLNK 2-(S-cysteinyl)-methionine (Cys-Met)</Feature>
-</Features>
-<Image src="/images/AA0559.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0559.PDB" />
-</Entry>
-<Entry id="AA0560">
-<Header>
-<Code>AA0560</Code>
-<Dates>
-<CreationDate>20-May-2011</CreationDate>
-<StrucRevDate>20-May-2011</StrucRevDate>
-<TextChngDate>20-Apr-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-(N-acetylamino)glucosyl-L-cysteine</Name>
-<AlternateName>S-[(N-acetylamino)glycosyl]cysteine</AlternateName>
-<AlternateName>S-[beta-D-(N-acetylamino)glucopyranosyl]cysteine</AlternateName>
-<SystematicName>(2R)-2-amino-3-(2-acetamido-2-deoxy-beta-D-glucopyranosylsulfanyl)propanoic acid</SystematicName>
-<Xref>CAS:10036-64-3</Xref>
-<Xref>ChEBI:61631</Xref>
-<Xref>PDBHET:NAG</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 11 H 18 N 2 O 6 S 1</Formula>
-<Weight type="chemical">306.33</Weight>
-<Weight type="physical">306.088557</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 8 H 13 N 1 O 5 S 0</Formula>
-<Weight type="chemical">203.19</Weight>
-<Weight type="physical">203.079373</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Stepper, J.</Author>
-<Author>Shastri, S.</Author>
-<Author>Loo, T.S.</Author>
-<Author>Preston, J.C.</Author>
-<Author>Novak, P.</Author>
-<Author>Man, P.</Author>
-<Author>Moore, C.H.</Author>
-<Author>Havlíček, V.</Author>
-<Author>Patchett, M.L.</Author>
-<Author>Norris, G.E.</Author>
-</Authors>
-<Citation>FEBS Lett. 585, 645-650, 2011</Citation>
-<Title>Cysteine S-glycosylation, a new post-translational modification found in glycopeptide bacteriocins.</Title>
-<Xref>DOI:10.1016/j.febslet.2011.01.023</Xref>
-<Xref>PMID:21251913</Xref>
-<Note>mass spectrometric detection</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Venugopal, H.</Author>
-<Author>Edwards, P.J.</Author>
-<Author>Schwalbe, M.</Author>
-<Author>Claridge, J.K.</Author>
-<Author>Libich, D.S.</Author>
-<Author>Stepper, J.</Author>
-<Author>Loo, T.</Author>
-<Author>Patchett, M.L.</Author>
-<Author>Norris, G.E.</Author>
-<Author>Pascal, S.M.</Author>
-</Authors>
-<Citation>Biochemistry 50, 2748-2755, 2011</Citation>
-<Title>Structural, dynamic, and chemical characterization of a novel s-glycosylated bacteriocin.</Title>
-<Xref>DOI:10.1021/bi200217u</Xref>
-<Xref>PMID:21395300</Xref>
-<Note>(1)H-NMR, (13)C-NMR and (15)N-NMR identification; stereochemical determination</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Venugopal, H.</Author>
-<Author>Edwards, P.</Author>
-<Author>Schwalbe, M.</Author>
-<Author>Claridge, J.</Author>
-<Author>Stepper, J.</Author>
-<Author>Patchett, M.</Author>
-<Author>Loo, T.</Author>
-<Author>Libich, D.</Author>
-<Author>Norris, G.</Author>
-<Author>Pascal, S.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, March 2010</Citation>
-<Description>Structure of glycocin A.</Description>
-<Xref>PDB:2KUY</Xref>
-<Note>NMR structural determination</Note>
-</ReferenceBlock>
-<Comment>See also RESID:AA0152 and RESID:AA0392 for other S-glycosylated cysteines.</Comment>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>PSI-MOD:01858</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__s-linked (glcnac)__c">CARBOHYD S-linked (GlcNAc)</Feature>
-<Feature type="UniProt" key="carbohyd__s-linked (glcnac...)__c">CARBOHYD S-linked (GlcNAc...)</Feature>
-<Feature type="UniProt" key="carbohyd__s-linked (hexnac...)__c">CARBOHYD S-linked (HexNAc...)</Feature>
-</Features>
-<Image src="/images/AA0560.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0560.PDB" />
-</Entry>
-<Entry id="AA0561">
-<Header>
-<Code>AA0561</Code>
-<Dates>
-<CreationDate>30-Sep-2011</CreationDate>
-<StrucRevDate>30-Sep-2011</StrucRevDate>
-<TextChngDate>30-Sep-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-(2-succinyl)-L-cysteine</Name>
-<AlternateName>(2R)-2-{[(2R)-2-amino-2-carboxyethyl]sulfanyl}butanedioic acid</AlternateName>
-<AlternateName>2-((2-amino-2-carboxyethyl)thio)butanedioic acid</AlternateName>
-<AlternateName>2-amino-3-(1,2-dicarboxyethylthio)propanoic acid</AlternateName>
-<AlternateName>S-(1,2-dicarboxyethyl)cysteine</AlternateName>
-<AlternateName>S-(2-succinyl)cysteine</AlternateName>
-<AlternateName>S-[(2R)-2-succinyl]-L-cysteine</AlternateName>
-<SystematicName>(2R)-2-amino-3-([(1R)-1,2-dicarboxyethyl]sulfanyl)propanoic acid</SystematicName>
-<Xref>CAS:34317-60-7</Xref>
-<Xref>PDBHET:SIN</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 9 N 1 O 5 S 1</Formula>
-<Weight type="chemical">219.21</Weight>
-<Weight type="physical">219.020143</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 4 H 4 N 0 O 4 S 0</Formula>
-<Weight type="chemical">116.07</Weight>
-<Weight type="physical">116.010959</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Alderson, N.L.</Author>
-<Author>Wang, Y.</Author>
-<Author>Blatnik, M.</Author>
-<Author>Frizzell, N.</Author>
-<Author>Walla, M.D.</Author>
-<Author>Lyons, T.J.</Author>
-<Author>Alt, N.</Author>
-<Author>Carson, J.A.</Author>
-<Author>Nagai, R.</Author>
-<Author>Thorpe, S.R.</Author>
-<Author>Baynes, J.W.</Author>
-</Authors>
-<Citation>Arch. Biochem. Biophys. 450, 1-8, 2006</Citation>
-<Title>S-(2-Succinyl)cysteine: a novel chemical modification of tissue proteins by a Krebs cycle intermediate.</Title>
-<Xref>DOI:10.1016/j.abb.2006.03.005</Xref>
-<Xref>PMID:16624247</Xref>
-<Note>chromatographic detection; mass spectrometric identification; identified as an advanced glycation artifact</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Blatnik, M.</Author>
-<Author>Thorpe, S.R.</Author>
-<Author>Baynes, J.W.</Author>
-</Authors>
-<Citation>Ann. N. Y. Acad. Sci. 1126, 272-275, 2008</Citation>
-<Title>Succination of proteins by fumarate: mechanism of inactivation of glyceraldehyde-3-phosphate dehydrogenase in diabetes.</Title>
-<Xref>DOI:10.1196/annals.1433.047</Xref>
-<Xref>PMID:18448829</Xref>
-<Note>mass spectrometric identification; identified as the active site cysteine inhibited product of glyceraldehyde-3-phosphate dehydrogenase; an artifact of diabetic stress</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fisch, F.</Author>
-<Author>Fleites, C.M.</Author>
-<Author>Delenne, M.</Author>
-<Author>Baudendistel, N.</Author>
-<Author>Hauer, B.</Author>
-<Author>Turkenburg, J.P.</Author>
-<Author>Hart, S.</Author>
-<Author>Bruce, N.C.</Author>
-<Author>Grogan, G.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 132, 11455-11457, 2010</Citation>
-<Title>A covalent succinylcysteine-like intermediate in the enzyme-catalyzed transformation of maleate to fumarate by maleate isomerase.</Title>
-<Xref>DOI:10.1021/ja1053576</Xref>
-<Xref>PMID:20677745</Xref>
-<Note>X-ray diffraction, 1.95 angstroms; directed mutation analysis; trapping of covalent intermediate</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fisch, F.</Author>
-<Author>Martinez-Fleites, C.</Author>
-<Author>Baudendistel, N.</Author>
-<Author>Hauer, B.</Author>
-<Author>Turkenburg, J.P.</Author>
-<Author>Hart, S.</Author>
-<Author>Bruce, N.C.</Author>
-<Author>Grogan, G.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, May 2010</Citation>
-<Description>Nocardia farcinica maleate cis-trans isomerase C194S mutant with A covalently bound succinylcysteine intermediate.</Description>
-<Xref>PDB:2XED</Xref>
-<Note>X-ray diffraction, 1.95 angstroms</Note>
-</ReferenceBlock>
-<Comment>This modification is produced in the active site inhibition of glyceraldehyde-3-phosphate dehydrogenase by fumarate, but as the active site intermediate in maleate isomerase.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>PSI-MOD:01889</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0561.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0561.PDB" />
-</Entry>
-<Entry id="AA0562">
-<Header>
-<Code>AA0562</Code>
-<Dates>
-<CreationDate>20-May-2011</CreationDate>
-<StrucRevDate>20-May-2011</StrucRevDate>
-<TextChngDate>30-Jun-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N,N-(L-cysteine-1,S-diyl)-L-phenylalanine</Name>
-<AlternateName>2-(4-amino-3-oxo-isothiazolidin-2-yl)-3-phenylpropanoic acid</AlternateName>
-<AlternateName>4-amino-3-isothiazolidinone-L-phenylalanine</AlternateName>
-<AlternateName>cysteinyl phenylalanine sulfenamide</AlternateName>
-<AlternateName>phenylalanine-cysteine sulfenyl amide cross-link</AlternateName>
-<AlternateName>phenylalanine-cysteine sulphenyl amide cross-link</AlternateName>
-<SystematicName>(2S)-2-[(4R)-4-amino-3-oxo-1,2-thiazolidin-2-yl]-3-phenylpropanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 12 H 12 N 2 O 2 S 1</Formula>
-<Weight type="chemical">248.30</Weight>
-<Weight type="physical">248.061949</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0014">
-<Formula>C 0 H -2 N 0 O 0 S 0</Formula>
-<Weight type="chemical">-2.02</Weight>
-<Weight type="physical">-2.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lee, J.W.</Author>
-<Author>Soonsanga, S.</Author>
-<Author>Helmann, J.D.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 104, 8743-8748, 2007</Citation>
-<Title>A complex thiolate switch regulates the Bacillus subtilis organic peroxide sensor OhrR.</Title>
-<Xref>DOI:10.1073/pnas.0702081104</Xref>
-<Xref>PMID:17502599</Xref>
-<Note>mass spectrometric detection; the modification is not chemically characterized</Note>
-</ReferenceBlock>
-<Comment>This cross-link is formed by the condensation of a cysteine residue sulfhydryl with the alpha-amido of the following residue.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C, F</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Xref>PSI-MOD:01859</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>isothiazole ring</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__n,n-(cysteine-1,s-diyl)phenylalanine (cys-phe)__c__f">CROSSLNK N,N-(cysteine-1,S-diyl)phenylalanine (Cys-Phe)</Feature>
-</Features>
-<Image src="/images/AA0562.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0562.PDB" />
-</Entry>
-<Entry id="AA0563">
-<Header>
-<Code>AA0563</Code>
-<Dates>
-<CreationDate>20-May-2011</CreationDate>
-<StrucRevDate>20-May-2011</StrucRevDate>
-<TextChngDate>30-Sep-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-cysteine bacillithiol disulfide</Name>
-<AlternateName>BSH</AlternateName>
-<AlternateName>BSH</AlternateName>
-<SystematicName>(2S)-(2-[S-(L-cystein-S-yl)-L-cysteinyl]amino-2-deoxy-alpha-D-glucopyranosyloxy)-butanedioic acid</SystematicName>
-<Xref>ChEBI:61338</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 16 H 25 N 3 O 11 S 2</Formula>
-<Weight type="chemical">499.51</Weight>
-<Weight type="physical">499.093051</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 13 H 20 N 2 O 10 S 1</Formula>
-<Weight type="chemical">396.37</Weight>
-<Weight type="physical">396.083866</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lee, J.W.</Author>
-<Author>Soonsanga, S.</Author>
-<Author>Helmann, J.D.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 104, 8743-8748, 2007</Citation>
-<Title>A complex thiolate switch regulates the Bacillus subtilis organic peroxide sensor OhrR.</Title>
-<Xref>DOI:10.1073/pnas.0702081104</Xref>
-<Xref>PMID:17502599</Xref>
-<Note>mass spectrometric detection; the modification is not chemically characterized</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Newton, G.L.</Author>
-<Author>Rawat, M.</Author>
-<Author>La Clair, J.J.</Author>
-<Author>Jothivasan, V.K.</Author>
-<Author>Budiarto, T.</Author>
-<Author>Hamilton, C.J.</Author>
-<Author>Claiborne, A.</Author>
-<Author>Helmann, J.D.</Author>
-<Author>Fahey, R.C.</Author>
-</Authors>
-<Citation>Nature Chem. Biol. 5, 625-627, 2009</Citation>
-<Title>Bacillithiol is an antioxidant thiol produced in Bacilli.</Title>
-<Xref>DOI:10.1038/nchembio.189</Xref>
-<Xref>PMID:19578333</Xref>
-<Note>mass spectrometric and (1)H-NMR identification; chemical characterization; naming</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>PSI-MOD:01860</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>disulfide bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__s-bacillithiol cysteine disulfide">MOD_RES S-bacillithiol cysteine disulfide</Feature>
-</Features>
-<Image src="/images/AA0563.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0563.PDB" />
-</Entry>
-<Entry id="AA0564">
-<Header>
-<Code>AA0564</Code>
-<Dates>
-<CreationDate>30-Jun-2011</CreationDate>
-<StrucRevDate>30-Jun-2011</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-deoxyhypusine</Name>
-<AlternateName>deoxyhypusine</AlternateName>
-<AlternateName>N6-(4-aminobutyl)lysine </AlternateName>
-<SystematicName>(2S)-2-amino-6-[(4-aminobutyl)amino]hexanoic acid</SystematicName>
-<Xref>CAS:82543-85-9</Xref>
-<Xref>ChEBI:91176</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 10 H 21 N 3 O 1</Formula>
-<Weight type="chemical">199.30</Weight>
-<Weight type="physical">199.168462</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 4 H 9 N 1 O 0</Formula>
-<Weight type="chemical">71.12</Weight>
-<Weight type="physical">71.073499</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Park, M.H.</Author>
-</Authors>
-<Citation>J. Biochem. 139, 161-169, 2006</Citation>
-<Title>The post-translational synthesis of a polyamine-derived amino acid, hypusine, in the eukaryotic translation initiation factor 5A (eIF5A).</Title>
-<Xref>DOI:10.1093/jb/mvj034</Xref>
-<Xref>PMID:16452303</Xref>
-<Note>review article</Note>
-</ReferenceBlock>
-<Comment>Deoxyhypusine is generated as an intermediate modification of initiation factor 5A, eIF5A, and as a modified lysine reaction intermediate in deoxyhypusine synthase before transfer of the 4-aminobutyl group.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-<EnzymeName>deoxyhypusine synthase (EC 2.5.1.46)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>GO:0034038</Xref>
-<Xref>PSI-MOD:01880</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0564.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0564.PDB" />
-</Entry>
-<Entry id="AA0565">
-<Header>
-<Code>AA0565</Code>
-<Dates>
-<CreationDate>30-Jun-2011</CreationDate>
-<StrucRevDate>30-Jun-2011</StrucRevDate>
-<TextChngDate>30-Jun-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>3-(L-phenylalan-2'-yl)-L-valine</Name>
-<AlternateName>symerythrin valine-phenylalanine cross-link</AlternateName>
-<SystematicName>(2S)-2-amino-4-(2-[(2S)-2-amino-2-carboxyethyl]phenyl)-3-methylbutanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 14 H 16 N 2 O 2</Formula>
-<Weight type="chemical">244.29</Weight>
-<Weight type="physical">244.121178</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0014 AA0020">
-<Formula>C 0 H -2 N 0 O 0</Formula>
-<Weight type="chemical">-2.02</Weight>
-<Weight type="physical">-2.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Cooley, R.B.</Author>
-<Author>Rhoads, T.W.</Author>
-<Author>Arp, D.J.</Author>
-<Author>Karplus, P.A.</Author>
-</Authors>
-<Citation>Science 332, 929, 2011</Citation>
-<Title>A diiron protein autogenerates a valine-phenylalanine cross-link.</Title>
-<Xref>DOI:10.1126/science.1205687</Xref>
-<Xref>PMID:21596985</Xref>
-<Note>X-ray diffraction, 1.20 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Cooley, R.B.</Author>
-<Author>Arp, D.J.</Author>
-<Author>Karplus, P.A.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, January 2011</Citation>
-<Description>Crystal structure of oxidized symerythrin from Cyanophora paradoxa.</Description>
-<Xref>PDB:3QHB</Xref>
-<Note>X-ray diffraction, 1.20 angstroms</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>F, V</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:01881</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0565.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0565.PDB" />
-</Entry>
-<Entry id="AA0566">
-<Header>
-<Code>AA0566</Code>
-<Dates>
-<CreationDate>30-Sep-2011</CreationDate>
-<StrucRevDate>30-Sep-2011</StrucRevDate>
-<TextChngDate>30-Sep-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-[(L-histidin-1'-yl)methyl]-L-methionine</Name>
-<SystematicName>(2S)-2-([(4-[(2S)-2-amino-2-carboxyethyl]-1H-imidazol-1-yl)methyl]amino)-4-(methylsulfanyl)butanoic acid</SystematicName>
-<Xref>PDBHET:FME</Xref>
-<Xref>PDBHET:HIC</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 12 H 17 N 4 O 2 S 1</Formula>
-<Weight type="chemical">281.35</Weight>
-<Weight type="physical">281.107222</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0009 AA0021" label="FMET">
-<Formula>C 0 H 0 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-16.00</Weight>
-<Weight type="physical">-15.994915</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0009 AA0013" label="MET">
-<Formula>C 1 H 0 N 0 O 0 S 0</Formula>
-<Weight type="chemical">12.01</Weight>
-<Weight type="physical">12.000000</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gregory, S.T.</Author>
-<Author>Demirci, H.</Author>
-<Author>Belardinelli, R.</Author>
-<Author>Monshupanee, T.</Author>
-<Author>Gualerzi, C.</Author>
-<Author>Dahlberg, A.E.</Author>
-<Author>Jogl, G.</Author>
-</Authors>
-<Citation>RNA 15, 1693-1704, 2009</Citation>
-<Title>Structural and functional studies of the Thermus thermophilus 16S rRNA methyltransferase RsmG.</Title>
-<Xref>DOI:10.1261/rna.1652709</Xref>
-<Xref>PMID:19622680</Xref>
-<Note>X-ray diffraction, 1.50 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Demirci, H.</Author>
-<Author>Gregory, S.T.</Author>
-<Author>Belardinelli, R.</Author>
-<Author>Gualerzi, C.</Author>
-<Author>Dahlberg, A.E.</Author>
-<Author>Jogl, G.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, February 2009</Citation>
-<Description>T. thermophilus 16S rRNA G527 methyltransferase in complex with AdoMet and AMP in space group P61.</Description>
-<Xref>PDB:3G89</Xref>
-<Note>X-ray diffraction, 1.50 angstroms</Note>
-</ReferenceBlock>
-<Comment>The electron density model has contradictory characteristics. The bond distances from the "formyl" carbon to the two nitrogens are in the single bond range, and the torsion angles around those bonds are not planar, suggesting that neither is a double bond. However, the bond angle between that carbon and the two nitrogens is closer to trigonal than to tetrahedral, suggesting sp2 hybridization. The modification is shown in a reduced state.</Comment>
-<Comment>Since both the source organism and the expression host encode N-formylmethionine initiator and the autocatalytic modification can occur before completion of translation, it is probable but not yet established that the modification occurs under natural conditions.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode link="FMET">
-<SequenceSpec>H, M</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:01890</Xref>
-</SequenceCode>
-<SequenceCode link="MET">
-<SequenceSpec>H, M</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:01891</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0566.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0566.PDB" />
-</Entry>
-<Entry id="AA0567">
-<Header>
-<Code>AA0567</Code>
-<Dates>
-<CreationDate>30-Sep-2011</CreationDate>
-<StrucRevDate>30-Sep-2011</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6-crotonyl-L-lysine</Name>
-<AlternateName>(2S)-2-amino-6-[(2E)-but-2-enamido]hexanoic acid</AlternateName>
-<AlternateName>(2S)-2-azanyl-6-[(2E)-but-2-enoylazanyl]hexanoic acid</AlternateName>
-<AlternateName>N(epsilon)-crotonyllysine</AlternateName>
-<AlternateName>N6-(E)-crotonyllysine</AlternateName>
-<AlternateName>N6-crotonyllysine</AlternateName>
-<AlternateName>N6-trans-crotonyllysine</AlternateName>
-<AlternateName>N6-[(2E)-2-butenoyl]-L-lysine</AlternateName>
-<SystematicName>(2S)-2-amino-6-[(2E)-but-2-enoylamino]hexanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 10 H 16 N 2 O 2</Formula>
-<Weight type="chemical">196.25</Weight>
-<Weight type="physical">196.121178</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 4 H 4 N 0 O 1</Formula>
-<Weight type="chemical">68.07</Weight>
-<Weight type="physical">68.026215</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Tan, M.</Author>
-<Author>Luo, H.</Author>
-<Author>Lee, S.</Author>
-<Author>Jin, F.</Author>
-<Author>Yang, J.S.</Author>
-<Author>Montellier, E.</Author>
-<Author>Buchou, T.</Author>
-<Author>Cheng, Z.</Author>
-<Author>Rousseaux, S.</Author>
-<Author>Rajagopal, N.</Author>
-<Author>Lu, Z.</Author>
-<Author>Ye, Z.</Author>
-<Author>Zhu, Q.</Author>
-<Author>Wysocka, J.</Author>
-<Author>Ye, Y.</Author>
-<Author>Khochbin, S.</Author>
-<Author>Ren, B.</Author>
-<Author>Zhao, Y.</Author>
-</Authors>
-<Citation>Cell 146, 1016-1028, 2011</Citation>
-<Title>Identification of 67 histone marks and histone lysine crotonylation as a new type of histone modification.</Title>
-<Xref>DOI:10.1016/j.cell.2011.08.008</Xref>
-<Xref>PMID:21925322</Xref>
-<Note>chromatographic and mass spectrometric identification; modification specific antibody</Note>
-</ReferenceBlock>
-<Comment>A metabolic source for crotonic acid or crotonyl-CoA in the nucleus is not evident, and a responsible enzyme activity is not identified.</Comment>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>PSI-MOD:01892</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Features>
-<Feature type="UniProt" key="mod_res__n6-crotonyllysine__k">MOD_RES N6-crotonyllysine</Feature>
-</Features>
-<Image src="/images/AA0567.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0567.PDB" />
-</Entry>
-<Entry id="AA0568">
-<Header>
-<Code>AA0568</Code>
-<Dates>
-<CreationDate>30-Sep-2011</CreationDate>
-<StrucRevDate>30-Sep-2011</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6-malonyl-L-lysine</Name>
-<AlternateName>2-azanyl-6-[(carboxyacetyl)azanyl]hexanoic acid</AlternateName>
-<AlternateName>malonyllysine</AlternateName>
-<AlternateName>N(epsilon)-(malonyl)lysine</AlternateName>
-<AlternateName>N6-(carboxyacetyl)lysine</AlternateName>
-<AlternateName>N6-malonyllysine</AlternateName>
-<SystematicName>(2S)-2-amino-6-[(carboxyacetyl)amino]hexanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 14 N 2 O 4</Formula>
-<Weight type="chemical">214.22</Weight>
-<Weight type="physical">214.095357</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 3 H 2 N 0 O 3</Formula>
-<Weight type="chemical">86.05</Weight>
-<Weight type="physical">86.000394</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Dalpozzo, A.</Author>
-<Author>Kanai, K.</Author>
-<Author>Kereszturi, G.</Author>
-<Author>Calabrese, G.</Author>
-</Authors>
-<Citation>Int. J. Pept. Protein Res. 41, 561-566, 1993</Citation>
-<Title>H-Gly-His psi (NHCO)Lys-OH, partially modified retro-inverso analogue of the growth factor glycyl-L-histidyl-L-lysine with enhanced enzymatic stability.</Title>
-<Xref>DOI:10.1111/j.1399-3011.1993.tb00478.x</Xref>
-<Xref>PMID:8349414</Xref>
-<Note>chemical synthesis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Peng, C.</Author>
-<Author>Lu, Z.</Author>
-<Author>Xie, Z.</Author>
-<Author>Cheng, Z.</Author>
-<Author>Chen, Y.</Author>
-<Author>Tan, M.</Author>
-<Author>Luo, H.</Author>
-<Author>Zhang, Y.</Author>
-<Author>He, W.</Author>
-<Author>Yang, K.</Author>
-<Author>Zwaans, B.M.</Author>
-<Author>Tishkoff, D.</Author>
-<Author>Ho, L.</Author>
-<Author>Lombard, D.</Author>
-<Author>He, T.C.</Author>
-<Author>Dai, J.</Author>
-<Author>Verdin, E.</Author>
-<Author>Ye, Y.</Author>
-<Author>Zhao, Y.</Author>
-</Authors>
-<Citation>Mol. Cell. Proteomics 10, M111.012658, 2011</Citation>
-<Title>The first identification of lysine malonylation substrates and its regulatory enzyme.</Title>
-<Xref>DOI:10.1074/mcp.M111.012658</Xref>
-<Xref>PMID:21908771</Xref>
-<Note>chromatographic and mass spectrometric identification; modification specific antibody</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Du, J.</Author>
-<Author>Zhou, Y.</Author>
-<Author>Su, X.</Author>
-<Author>Yu, J.J.</Author>
-<Author>Khan, S.</Author>
-<Author>Jiang, H.</Author>
-<Author>Kim, J.</Author>
-<Author>Woo, J.</Author>
-<Author>Kim, J.H.</Author>
-<Author>Choi, B.H.</Author>
-<Author>He, B.</Author>
-<Author>Chen, W.</Author>
-<Author>Zhang, S.</Author>
-<Author>Cerione, R.A.</Author>
-<Author>Auwerx, J.</Author>
-<Author>Hao, Q.</Author>
-<Author>Lin, H.</Author>
-</Authors>
-<Citation>Science 334, 806-809, 2011</Citation>
-<Title>Sirt5 is a NAD-dependent protein lysine demalonylase and desuccinylase.</Title>
-<Xref>DOI:10.1126/science.1207861</Xref>
-<Xref>PMID:22076378</Xref>
-<Note>mass spectrometric identification in a number of mitochondrial proteins; identification of Sirt5 as a demalonylase</Note>
-</ReferenceBlock>
-<Comment>The responsible generating enzyme activity is not identified. This modification can be reversed by Sirt5.</Comment>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>GO:0044392</Xref>
-<Xref>PSI-MOD:01893</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="mod_res__n6-malonyllysine__k">MOD_RES N6-malonyllysine</Feature>
-</Features>
-<Image src="/images/AA0568.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0568.PDB" />
-</Entry>
-<Entry id="AA0569">
-<Header>
-<Code>AA0569</Code>
-<Dates>
-<CreationDate>28-Oct-2011</CreationDate>
-<StrucRevDate>28-Oct-2011</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N2,N2-dimethyl-L-arginine</Name>
-<AlternateName>(2S)-5-carbamimidamido-2-(dimethylamino)pentanoic acid [tautomer]</AlternateName>
-<AlternateName>N(alpha),N(alpha)-dimethylarginine</AlternateName>
-<AlternateName>N2,N2-dimethylarginine</AlternateName>
-<SystematicName>(2S)-5-[(diaminomethylidene)amino]-2-(dimethylamino)pentanoic acid</SystematicName>
-<Xref>CAS:190784-00-0</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 8 H 17 N 4 O 1</Formula>
-<Weight type="chemical">185.25</Weight>
-<Weight type="physical">185.140236</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0002">
-<Formula>C 2 H 4 N 0 O 0</Formula>
-<Weight type="chemical">28.05</Weight>
-<Weight type="physical">28.031300</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kalyon, B.</Author>
-<Author>Helaly, S.E.</Author>
-<Author>Scholz, R.</Author>
-<Author>Nachtigall, J.</Author>
-<Author>Vater, J.</Author>
-<Author>Borriss, R.</Author>
-<Author>Süssmuth, R.D.</Author>
-</Authors>
-<Citation>Org. Lett. 13, 2996-2999, 2011</Citation>
-<Title>Plantazolicin A and B: Structure Elucidation of Ribosomally Synthesized Thiazole/Oxazole Peptides from Bacillus amyloliquefaciens FZB42.</Title>
-<Xref>DOI:10.1021/ol200809m</Xref>
-<Xref>PMID:21568297</Xref>
-<Note>mass spectrometric, (1)H-NMR, (13)C-NMR and (15)N-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Molohon, K.J.</Author>
-<Author>Melby, J.O.</Author>
-<Author>Lee, J.</Author>
-<Author>Evans, B.S.</Author>
-<Author>Dunbar, K.L.</Author>
-<Author>Bumpus, S.B.</Author>
-<Author>Kelleher, N.L.</Author>
-<Author>Mitchell, D.A.</Author>
-</Authors>
-<Citation>ACS Chem. Biol. 6, 1307-1313, 2011</Citation>
-<Title>Structure determination and interception of biosynthetic intermediates for the plantazolicin class of highly discriminating antibiotics.</Title>
-<Xref>DOI:10.1021/cb200339d</Xref>
-<Xref>PMID:21950656</Xref>
-<Note>mass spectrometric, (1)H-NMR and (13)C-NMR identification</Note>
-</ReferenceBlock>
-<Comment>This modification should not be confused with omega-N,omega-N'-dimethyl-L-arginine (see RESID:AA0067) or omega-N,omega-N-dimethyl-L-arginine (see RESID:AA0068).</Comment>
-<GeneratingEnzyme>
-<EnzymeName>protein N-terminal methyltransferase (EC 2.1.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>R</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>PSI-MOD:01898</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-<Keyword>methylated amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n2,n2-dimethylarginine">MOD_RES N2,N2-dimethylarginine</Feature>
-</Features>
-<Image src="/images/AA0569.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0569.PDB" />
-</Entry>
-<Entry id="AA0570">
-<Header>
-<Code>AA0570</Code>
-<Dates>
-<CreationDate>28-Oct-2011</CreationDate>
-<StrucRevDate>28-Oct-2011</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-arginine thiazole-4-carboxylic acid</Name>
-<SystematicName>2-[(1S)-1-amino-4-([diaminomethylidene]amino)butyl]-1,3-thiazole-4-carboxylic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 13 N 5 O 1 S 1</Formula>
-<Weight type="chemical">239.30</Weight>
-<Weight type="physical">239.084081</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0002 AA0005">
-<Formula>C 0 H -4 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-20.03</Weight>
-<Weight type="physical">-20.026215</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kalyon, B.</Author>
-<Author>Helaly, S.E.</Author>
-<Author>Scholz, R.</Author>
-<Author>Nachtigall, J.</Author>
-<Author>Vater, J.</Author>
-<Author>Borriss, R.</Author>
-<Author>Süssmuth, R.D.</Author>
-</Authors>
-<Citation>Org. Lett. 13, 2996-2999, 2011</Citation>
-<Title>Plantazolicin A and B: Structure Elucidation of Ribosomally Synthesized Thiazole/Oxazole Peptides from Bacillus amyloliquefaciens FZB42.</Title>
-<Xref>DOI:10.1021/ol200809m</Xref>
-<Xref>PMID:21568297</Xref>
-<Note>mass spectrometric, (1)H-NMR, (13)C-NMR and (15)N-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Molohon, K.J.</Author>
-<Author>Melby, J.O.</Author>
-<Author>Lee, J.</Author>
-<Author>Evans, B.S.</Author>
-<Author>Dunbar, K.L.</Author>
-<Author>Bumpus, S.B.</Author>
-<Author>Kelleher, N.L.</Author>
-<Author>Mitchell, D.A.</Author>
-</Authors>
-<Citation>ACS Chem. Biol. 6, 1307-1313, 2011</Citation>
-<Title>Structure determination and interception of biosynthetic intermediates for the plantazolicin class of highly discriminating antibiotics.</Title>
-<Xref>DOI:10.1021/cb200339d</Xref>
-<Xref>PMID:21950656</Xref>
-<Note>mass spectrometric, (1)H-NMR and (13)C-NMR identification</Note>
-</ReferenceBlock>
-<Comment>Formed by the condensation of a cysteine thiol with the carbonyl of the preceding residue and alpha-beta dehydrogenation.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptidyl-cysteine cyclase (EC 4.2.1.-)</EnzymeName>
-<EnzymeName>peptidyl-thiazoline dehydrogenase (EC 1.3.-.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C, R</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Xref>PSI-MOD:01899</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>oxazole/thiazole ring</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__thiazole-4-carboxylic acid ?arg-cys?__r__c">CROSSLNK Thiazole-4-carboxylic acid (Arg-Cys)</Feature>
-</Features>
-<Image src="/images/AA0570.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0570.PDB" />
-</Entry>
-<Entry id="AA0571">
-<Header>
-<Code>AA0571</Code>
-<Dates>
-<CreationDate>28-Oct-2011</CreationDate>
-<StrucRevDate>28-Oct-2011</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-cysteine 5-methyloxazole-4-carboxylic acid</Name>
-<AlternateName>2-[(1R)-1-azanyl-2-sulfanylethyl]-5-methyl-1,3-oxazole-4-carboxylic acid</AlternateName>
-<SystematicName>2-[(1R)-1-amino-2-sulfanylethyl]-5-methyl-1,3-oxazole-4-carboxylic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 8 N 2 O 2 S 1</Formula>
-<Weight type="chemical">184.21</Weight>
-<Weight type="physical">184.030649</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0017">
-<Formula>C 0 H -4 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-20.03</Weight>
-<Weight type="physical">-20.026215</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kalyon, B.</Author>
-<Author>Helaly, S.E.</Author>
-<Author>Scholz, R.</Author>
-<Author>Nachtigall, J.</Author>
-<Author>Vater, J.</Author>
-<Author>Borriss, R.</Author>
-<Author>Süssmuth, R.D.</Author>
-</Authors>
-<Citation>Org. Lett. 13, 2996-2999, 2011</Citation>
-<Title>Plantazolicin A and B: Structure Elucidation of Ribosomally Synthesized Thiazole/Oxazole Peptides from Bacillus amyloliquefaciens FZB42.</Title>
-<Xref>DOI:10.1021/ol200809m</Xref>
-<Xref>PMID:21568297</Xref>
-<Note>mass spectrometric, (1)H-NMR, (13)C-NMR and (15)N-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Molohon, K.J.</Author>
-<Author>Melby, J.O.</Author>
-<Author>Lee, J.</Author>
-<Author>Evans, B.S.</Author>
-<Author>Dunbar, K.L.</Author>
-<Author>Bumpus, S.B.</Author>
-<Author>Kelleher, N.L.</Author>
-<Author>Mitchell, D.A.</Author>
-</Authors>
-<Citation>ACS Chem. Biol. 6, 1307-1313, 2011</Citation>
-<Title>Structure determination and interception of biosynthetic intermediates for the plantazolicin class of highly discriminating antibiotics.</Title>
-<Xref>DOI:10.1021/cb200339d</Xref>
-<Xref>PMID:21950656</Xref>
-<Note>mass spectrometric, (1)H-NMR and (13)C-NMR identification</Note>
-</ReferenceBlock>
-<Comment>Formed by the condensation of a cysteine thiol with the carbonyl of the preceding residue and alpha-beta dehydrogenation.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptidyl-threonine cyclase (EC 4.2.1.-)</EnzymeName>
-<EnzymeName>peptidyl-oxazoline dehydrogenase (EC 1.3.-.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C, T</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Xref>PSI-MOD:01900</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>oxazole/thiazole ring</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__5-methyloxazole-4-carboxylic acid ?cys-thr?__c__t">CROSSLNK 5-methyloxazole-4-carboxylic acid (Cys-Thr)</Feature>
-</Features>
-<Image src="/images/AA0571.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0571.PDB" />
-</Entry>
-<Entry id="AA0572">
-<Header>
-<Code>AA0572</Code>
-<Dates>
-<CreationDate>28-Oct-2011</CreationDate>
-<StrucRevDate>28-Oct-2011</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-threonine 5-methyloxazole-4-carboxylic acid</Name>
-<AlternateName>2-[(1S,2R)-1-azanyl-2-hydroxypropyl]-5-methyl-1,3-oxazole-4-carboxylic acid</AlternateName>
-<SystematicName>2-[(1S,2R)-1-amino-2-hydroxypropyl]-5-methyl-1,3-oxazole-4-carboxylic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 8 H 10 N 2 O 3</Formula>
-<Weight type="chemical">182.18</Weight>
-<Weight type="physical">182.069142</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0017 AA0017">
-<Formula>C 0 H -4 N 0 O -1</Formula>
-<Weight type="chemical">-20.03</Weight>
-<Weight type="physical">-20.026215</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kalyon, B.</Author>
-<Author>Helaly, S.E.</Author>
-<Author>Scholz, R.</Author>
-<Author>Nachtigall, J.</Author>
-<Author>Vater, J.</Author>
-<Author>Borriss, R.</Author>
-<Author>Süssmuth, R.D.</Author>
-</Authors>
-<Citation>Org. Lett. 13, 2996-2999, 2011</Citation>
-<Title>Plantazolicin A and B: Structure Elucidation of Ribosomally Synthesized Thiazole/Oxazole Peptides from Bacillus amyloliquefaciens FZB42.</Title>
-<Xref>DOI:10.1021/ol200809m</Xref>
-<Xref>PMID:21568297</Xref>
-<Note>mass spectrometric, (1)H-NMR, (13)C-NMR and (15)N-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Molohon, K.J.</Author>
-<Author>Melby, J.O.</Author>
-<Author>Lee, J.</Author>
-<Author>Evans, B.S.</Author>
-<Author>Dunbar, K.L.</Author>
-<Author>Bumpus, S.B.</Author>
-<Author>Kelleher, N.L.</Author>
-<Author>Mitchell, D.A.</Author>
-</Authors>
-<Citation>ACS Chem. Biol. 6, 1307-1313, 2011</Citation>
-<Title>Structure determination and interception of biosynthetic intermediates for the plantazolicin class of highly discriminating antibiotics.</Title>
-<Xref>DOI:10.1021/cb200339d</Xref>
-<Xref>PMID:21950656</Xref>
-<Note>mass spectrometric, (1)H-NMR and (13)C-NMR identification</Note>
-</ReferenceBlock>
-<Comment>Formed by the condensation of a cysteine thiol with the carbonyl of the preceding residue and alpha-beta dehydrogenation.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptidyl-threonine cyclase (EC 4.2.1.-)</EnzymeName>
-<EnzymeName>peptidyl-oxazoline dehydrogenase (EC 1.3.-.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>T, T</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Xref>PSI-MOD:01901</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>oxazole/thiazole ring</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__5-methyloxazole-4-carboxylic acid (thr-thr)__t__t">CROSSLNK 5-methyloxazole-4-carboxylic acid (Thr-Thr)</Feature>
-</Features>
-<Image src="/images/AA0572.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0572.PDB" />
-</Entry>
-<Entry id="AA0573">
-<Header>
-<Code>AA0573</Code>
-<Dates>
-<CreationDate>28-Oct-2011</CreationDate>
-<StrucRevDate>28-Oct-2011</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-isoleucine oxazole-4-carboxylic acid</Name>
-<AlternateName>2-[(1S,2S)-1-azanyl-2-methylbutyl]-1,3-oxazole-4-carboxylic acid</AlternateName>
-<SystematicName>2-[(1S,2S)-1-amino-2-methylbutyl]-1,3-oxazole-4-carboxylic acid </SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 12 N 2 O 2</Formula>
-<Weight type="chemical">180.21</Weight>
-<Weight type="physical">180.089878</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0010 AA0016">
-<Formula>C 0 H -4 N 0 O -1</Formula>
-<Weight type="chemical">-20.03</Weight>
-<Weight type="physical">-20.026215</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kalyon, B.</Author>
-<Author>Helaly, S.E.</Author>
-<Author>Scholz, R.</Author>
-<Author>Nachtigall, J.</Author>
-<Author>Vater, J.</Author>
-<Author>Borriss, R.</Author>
-<Author>Süssmuth, R.D.</Author>
-</Authors>
-<Citation>Org. Lett. 13, 2996-2999, 2011</Citation>
-<Title>Plantazolicin A and B: Structure Elucidation of Ribosomally Synthesized Thiazole/Oxazole Peptides from Bacillus amyloliquefaciens FZB42.</Title>
-<Xref>DOI:10.1021/ol200809m</Xref>
-<Xref>PMID:21568297</Xref>
-<Note>mass spectrometric, (1)H-NMR, (13)C-NMR and (15)N-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Molohon, K.J.</Author>
-<Author>Melby, J.O.</Author>
-<Author>Lee, J.</Author>
-<Author>Evans, B.S.</Author>
-<Author>Dunbar, K.L.</Author>
-<Author>Bumpus, S.B.</Author>
-<Author>Kelleher, N.L.</Author>
-<Author>Mitchell, D.A.</Author>
-</Authors>
-<Citation>ACS Chem. Biol. 6, 1307-1313, 2011</Citation>
-<Title>Structure determination and interception of biosynthetic intermediates for the plantazolicin class of highly discriminating antibiotics.</Title>
-<Xref>DOI:10.1021/cb200339d</Xref>
-<Xref>PMID:21950656</Xref>
-<Note>mass spectrometric, (1)H-NMR and (13)C-NMR identification</Note>
-</ReferenceBlock>
-<Comment>Formed by the condensation of a cysteine thiol with the carbonyl of the preceding residue and alpha-beta dehydrogenation.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptidyl-serine cyclase (EC 4.2.1.-)</EnzymeName>
-<EnzymeName>peptidyl-oxazoline dehydrogenase (EC 1.3.-.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>I, S</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Xref>PSI-MOD:01902</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>oxazole/thiazole ring</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__oxazole-4-carboxylic acid (ile-ser)__i__s">CROSSLNK Oxazole-4-carboxylic acid (Ile-Ser)</Feature>
-</Features>
-<Image src="/images/AA0573.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0573.PDB" />
-</Entry>
-<Entry id="AA0574">
-<Header>
-<Code>AA0574</Code>
-<Dates>
-<CreationDate>28-Oct-2011</CreationDate>
-<StrucRevDate>28-Oct-2011</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-serine oxazole-4-carboxylic acid</Name>
-<AlternateName>2-[(1S)-1-azanyl-2-hydroxyethyl]-1,3-oxazole-4-carboxylic acid </AlternateName>
-<SystematicName>2-[(1S)-1-amino-2-hydroxyethyl]-1,3-oxazole-4-carboxylic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 6 N 2 O 3</Formula>
-<Weight type="chemical">154.13</Weight>
-<Weight type="physical">154.037842</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016 AA0016">
-<Formula>C 0 H -4 N 0 O -1</Formula>
-<Weight type="chemical">-20.03</Weight>
-<Weight type="physical">-20.026215</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kalyon, B.</Author>
-<Author>Helaly, S.E.</Author>
-<Author>Scholz, R.</Author>
-<Author>Nachtigall, J.</Author>
-<Author>Vater, J.</Author>
-<Author>Borriss, R.</Author>
-<Author>Süssmuth, R.D.</Author>
-</Authors>
-<Citation>Org. Lett. 13, 2996-2999, 2011</Citation>
-<Title>Plantazolicin A and B: Structure Elucidation of Ribosomally Synthesized Thiazole/Oxazole Peptides from Bacillus amyloliquefaciens FZB42.</Title>
-<Xref>DOI:10.1021/ol200809m</Xref>
-<Xref>PMID:21568297</Xref>
-<Note>mass spectrometric, (1)H-NMR, (13)C-NMR and (15)N-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Molohon, K.J.</Author>
-<Author>Melby, J.O.</Author>
-<Author>Lee, J.</Author>
-<Author>Evans, B.S.</Author>
-<Author>Dunbar, K.L.</Author>
-<Author>Bumpus, S.B.</Author>
-<Author>Kelleher, N.L.</Author>
-<Author>Mitchell, D.A.</Author>
-</Authors>
-<Citation>ACS Chem. Biol. 6, 1307-1313, 2011</Citation>
-<Title>Structure determination and interception of biosynthetic intermediates for the plantazolicin class of highly discriminating antibiotics.</Title>
-<Xref>DOI:10.1021/cb200339d</Xref>
-<Xref>PMID:21950656</Xref>
-<Note>mass spectrometric, (1)H-NMR and (13)C-NMR identification</Note>
-</ReferenceBlock>
-<Comment>Formed by the condensation of a cysteine thiol with the carbonyl of the preceding residue and alpha-beta dehydrogenation.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptidyl-serine cyclase (EC 4.2.1.-)</EnzymeName>
-<EnzymeName>peptidyl-oxazoline dehydrogenase (EC 1.3.-.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>S, S</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Xref>PSI-MOD:01903</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>oxazole/thiazole ring</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__oxazole-4-carboxylic acid (ser-ser)__s__s">CROSSLNK Oxazole-4-carboxylic acid (Ser-Ser)</Feature>
-</Features>
-<Image src="/images/AA0574.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0574.PDB" />
-</Entry>
-<Entry id="AA0575">
-<Header>
-<Code>AA0575</Code>
-<Dates>
-<CreationDate>28-Oct-2011</CreationDate>
-<StrucRevDate>28-Oct-2011</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-serine 5-methyloxazoline-4-carboxylic acid</Name>
-<AlternateName>2-[(1S)-1-amino-2-hydroxyethyl]-5-methyl-1,3-oxazoline-4-carboxylic acid</AlternateName>
-<AlternateName>2-[(1S)-1-azanyl-2-hydroxyethyl]-5-methyl-4,5-dihydro-1,3-oxazole-4-carboxylic acid</AlternateName>
-<SystematicName>2-[(1S)-1-amino-2-hydroxyethyl]-5-methyl-4,5-dihydro-1,3-oxazole-4-carboxylic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 10 N 2 O 3</Formula>
-<Weight type="chemical">170.17</Weight>
-<Weight type="physical">170.069142</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016 AA0017">
-<Formula>C 0 H -2 N 0 O -1</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kalyon, B.</Author>
-<Author>Helaly, S.E.</Author>
-<Author>Scholz, R.</Author>
-<Author>Nachtigall, J.</Author>
-<Author>Vater, J.</Author>
-<Author>Borriss, R.</Author>
-<Author>Süssmuth, R.D.</Author>
-</Authors>
-<Citation>Org. Lett. 13, 2996-2999, 2011</Citation>
-<Title>Plantazolicin A and B: Structure Elucidation of Ribosomally Synthesized Thiazole/Oxazole Peptides from Bacillus amyloliquefaciens FZB42.</Title>
-<Xref>DOI:10.1021/ol200809m</Xref>
-<Xref>PMID:21568297</Xref>
-<Note>mass spectrometric, (1)H-NMR, (13)C-NMR and (15)N-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Molohon, K.J.</Author>
-<Author>Melby, J.O.</Author>
-<Author>Lee, J.</Author>
-<Author>Evans, B.S.</Author>
-<Author>Dunbar, K.L.</Author>
-<Author>Bumpus, S.B.</Author>
-<Author>Kelleher, N.L.</Author>
-<Author>Mitchell, D.A.</Author>
-</Authors>
-<Citation>ACS Chem. Biol. 6, 1307-1313, 2011</Citation>
-<Title>Structure determination and interception of biosynthetic intermediates for the plantazolicin class of highly discriminating antibiotics.</Title>
-<Xref>DOI:10.1021/cb200339d</Xref>
-<Xref>PMID:21950656</Xref>
-<Note>mass spectrometric, (1)H-NMR and (13)C-NMR identification</Note>
-</ReferenceBlock>
-<Comment>Formed by the condensation of a cysteine thiol with the carbonyl of the preceding residue and alpha-beta dehydrogenation.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptidyl-threonine cyclase (EC 4.2.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>S, T</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Xref>PSI-MOD:01904</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>oxazole/thiazole ring</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__5-methyloxazoline-4-carboxylic acid (ser-thr)__t__t">CROSSLNK 5-methyloxazoline-4-carboxylic acid (Ser-Thr)</Feature>
-</Features>
-<Image src="/images/AA0575.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0575.PDB" />
-</Entry>
-<Entry id="AA0576">
-<Header>
-<Code>AA0576</Code>
-<Dates>
-<CreationDate>31-Dec-2011</CreationDate>
-<StrucRevDate>31-Dec-2011</StrucRevDate>
-<TextChngDate>31-Dec-2011</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-formyl-L-alanine</Name>
-<AlternateName>2-formamidopropanoic acid</AlternateName>
-<AlternateName>2-formamidopropionic acid</AlternateName>
-<SystematicName>(2S)-2-(formylamino)propanoic acid</SystematicName>
-<Xref>CAS:10512-86-4</Xref>
-<Xref>PDBHET:FOR</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 6 N 1 O 2</Formula>
-<Weight type="chemical">100.10</Weight>
-<Weight type="physical">100.039853</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0001">
-<Formula>C 1 H 0 N 0 O 1</Formula>
-<Weight type="chemical">28.01</Weight>
-<Weight type="physical">27.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Transue, T.R.</Author>
-<Author>Smith, A.K.</Author>
-<Author>Mo, H.</Author>
-<Author>Goldstein, I.J.</Author>
-<Author>Saper, M.A.</Author>
-</Authors>
-<Citation>Nature Struct. Biol. 4, 779-783, 1997</Citation>
-<Title>Structure of benzyl T-antigen disaccharide bound to Amaranthus caudatus agglutinin.</Title>
-<Xref>DOI:10.1038/nsb1097-779</Xref>
-<Xref>PMID:9334739</Xref>
-<Note>X-ray diffraction, 2.20 angstroms; the amino-terminal is blocked; there is no chemical evidence for the identity of the blocking group; a formyl group fits the electron density</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Transue, T.R.</Author>
-<Author>Smith, A.K.</Author>
-<Author>Mo, H.</Author>
-<Author>Goldstein, I.J.</Author>
-<Author>Saper, M.A.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, July 1997</Citation>
-<Description>Crystal structure of Amaranthus caudatus agglutinin.</Description>
-<Xref>PDB:1JLY</Xref>
-<Note>X-ray diffraction, 2.20 angstroms</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>A</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>PSI-MOD:01915</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-<Keyword>formylation</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0576.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0576.PDB" />
-</Entry>
-<Entry id="AA0577">
-<Header>
-<Code>AA0577</Code>
-<Dates>
-<CreationDate>31-Dec-2011</CreationDate>
-<StrucRevDate>31-Dec-2011</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O4'-(N-acetylamino)galactosyl-L-tyrosine</Name>
-<AlternateName>mucin type O-glycosyltyrosine</AlternateName>
-<AlternateName>O4'-(N-acetylgalactosaminyl)tyrosine</AlternateName>
-<AlternateName>O4'-glycosyl-L-tyrosine</AlternateName>
-<SystematicName>(2S)-2-amino-3-[4-(2-acetamido-2-deoxy-beta-D-galactopyranosyloxy)phenyl]propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 17 H 22 N 2 O 7 +</Formula>
-<Weight type="chemical">366.37 +</Weight>
-<Weight type="physical">366.142701 +</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0019">
-<Formula>C 8 H 13 N 1 O 5 +</Formula>
-<Weight type="chemical">203.19 +</Weight>
-<Weight type="physical">203.079373 +</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Halim, A.</Author>
-<Author>Brinkmalm, G.</Author>
-<Author>Rüetschi, U.</Author>
-<Author>Westman-Brinkmalm, A.</Author>
-<Author>Portelius, E.</Author>
-<Author>Zetterberg, H.</Author>
-<Author>Blennow, K.</Author>
-<Author>Larson, G.</Author>
-<Author>Nilsson, J.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 108, 11848-11853, 2011</Citation>
-<Title>Site-specific characterization of threonine, serine, and tyrosine glycosylations of amyloid precursor protein/amyloid beta-peptides in human cerebrospinal fluid.</Title>
-<Xref>DOI:10.1073/pnas.1102664108</Xref>
-<Xref>PMID:21712440</Xref>
-<Note>mass spectrometric detection</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Steentoft, C.</Author>
-<Author>Vakhrushev, S.Y.</Author>
-<Author>Vester-Christensen, M.B.</Author>
-<Author>Schjoldager, K.T.</Author>
-<Author>Kong, Y.</Author>
-<Author>Bennett, E.P.</Author>
-<Author>Mandel, U.</Author>
-<Author>Wandall, H.</Author>
-<Author>Levery, S.B.</Author>
-<Author>Clausen, H.</Author>
-</Authors>
-<Citation>Nature Methods 8, 977-982, 2011</Citation>
-<Title>Mining the O-glycoproteome using zinc-finger nuclease-glycoengineered SimpleCell lines.</Title>
-<Xref>DOI:10.1038/nmeth.1731</Xref>
-<Xref>PMID:21983924</Xref>
-<Note>mass spectrometric detection; assumed to be (N-acetylamino)galactose in alpha linkage because of the disialylated core structure</Note>
-</ReferenceBlock>
-<Comment>The alpha anomeric form is shown.</Comment>
-<Comment>See also RESID:AA0157 for other O-glycosylated tyrosines.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>polypeptide N-acetylgalactosaminyltransferase (EC 2.4.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>Y</SequenceSpec>
-<Xref>PSI-MOD:01916</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="carbohyd__o-linked (galnac) tyrosine__y">CARBOHYD O-linked (GalNAc) tyrosine</Feature>
-<Feature type="UniProt" key="carbohyd__o-linked (galnac...) tyrosine__y">CARBOHYD O-linked (GalNAc...) tyrosine</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="carbohyd__o-linked (hexnac...) tyrosine__y">CARBOHYD O-linked (HexNAc...) tyrosine</Feature>
-<Note>this UniProt feature is used when the identity of the sugar has not been determined</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0577.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0577.PDB" />
-</Entry>
-<Entry id="AA0578">
-<Header>
-<Code>AA0578</Code>
-<Dates>
-<CreationDate>31-Mar-2012</CreationDate>
-<StrucRevDate>31-Mar-2012</StrucRevDate>
-<TextChngDate>31-Mar-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>(2S,5S)-5-hydroxylysine</Name>
-<AlternateName>2,6-bisazanyl-5-hydroxyhexanoic acid</AlternateName>
-<AlternateName>2,6-diamino-2,3,4,6-tetradeoxyhexonic acid</AlternateName>
-<AlternateName>alpha,epsilon-diamino-delta-hydroxycaproic acid</AlternateName>
-<AlternateName>L-allo-delta-hydroxylysine</AlternateName>
-<AlternateName>L-threo-delta-hydroxylysine</AlternateName>
-<SystematicName>(2S,5S)-2,6-diamino-5-hydroxyhexanoic acid</SystematicName>
-<Xref>CAS:18899-29-1</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 12 N 2 O 2</Formula>
-<Weight type="chemical">144.17</Weight>
-<Weight type="physical">144.089878</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 0 H 0 N 0 O 1</Formula>
-<Weight type="chemical">16.00</Weight>
-<Weight type="physical">15.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Webby, C.J.</Author>
-<Author>Wolf, A.</Author>
-<Author>Gromak, N.</Author>
-<Author>Dreger, M.</Author>
-<Author>Kramer, H.</Author>
-<Author>Kessler, B.</Author>
-<Author>Nielsen, M.L.</Author>
-<Author>Schmitz, C.</Author>
-<Author>Butler, D.S.</Author>
-<Author>Yates 3rd, J.R.</Author>
-<Author>Delahunty, C.M.</Author>
-<Author>Hahn, P.</Author>
-<Author>Lengeling, A.</Author>
-<Author>Mann, M.</Author>
-<Author>Proudfoot, N.J.</Author>
-<Author>Schofield, C.J.</Author>
-<Author>Böttger, A.</Author>
-</Authors>
-<Citation>Science 325, 90-93, 2009</Citation>
-<Title>Jmjd6 Catalyses Lysyl-Hydroxylation of U2AF65, a Protein Associated with RNA Splicing.</Title>
-<Xref>DOI:10.1126/science.1175865</Xref>
-<Xref>PMID:19574390</Xref>
-<Note>identification of JMJD6 (Jumonji domain-6) protein as a lysyl-5-hydroxylase acting on U2AF65; JMJD6 had earlier been identified as an iron and 2-oxoglutarate-dependent oxygenase acting as a histone arginine demethylase</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mantri, M.</Author>
-<Author>Loik, N.D.</Author>
-<Author>Hamed, R.B.</Author>
-<Author>Claridge, T.D.</Author>
-<Author>McCullagh, J.S.</Author>
-<Author>Schofield, C.J.</Author>
-</Authors>
-<Citation>Chembiochem 12, 531-534, 2011</Citation>
-<Title>The 2-Oxoglutarate-Dependent Oxygenase JMJD6 Catalyses Oxidation of Lysine Residues to give 5S-Hydroxylysine Residues.</Title>
-<Xref>DOI:10.1002/cbic.201000641</Xref>
-<Xref>PMID:22238144</Xref>
-<Note>synthesis of diastereomers, and (1)H-NMR identification</Note>
-</ReferenceBlock>
-<Comment>This diastereomeric form has been found in some splicing regulatory proteins. For the (2S,5R)-diastereomer, see RESID:AA0028.</Comment>
-<Comment>The Enzyme Commission has not yet distinguished the different stereospecific enzyme activities.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptide-lysine 5-dioxygenase JMJD6 (EC 1.14.11.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>PSI-MOD:01918</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__?5s?-5-hydroxylysine__k">MOD_RES (5S)-5-hydroxylysine</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="mod_res__5-hydroxylysine__k">MOD_RES 5-hydroxylysine</Feature>
-<Note>this UniProt feature is used when the stereochemistry has not been determined</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0578.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0578.PDB" />
-</Entry>
-<Entry id="AA0579">
-<Header>
-<Code>AA0579</Code>
-<Dates>
-<CreationDate>31-Mar-2012</CreationDate>
-<StrucRevDate>31-Mar-2012</StrucRevDate>
-<TextChngDate>01-Mar-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>(2S,3S)-3-hydroxyaspartic acid</Name>
-<AlternateName>(3S)-3-hydroxy-L-aspartic acid</AlternateName>
-<AlternateName>2-amino-3-hydroxysuccinic acid</AlternateName>
-<AlternateName>2-azanyl-3-hydroxybutanedioic acid</AlternateName>
-<AlternateName>3-hydroxyaspartic acid</AlternateName>
-<AlternateName>L-threo-3-hydroxyaspartic acid</AlternateName>
-<AlternateName>L-threo-beta-hydroxyaspartic acid</AlternateName>
-<SystematicName>(2S,3S)-2-amino-3-hydroxybutanedioic acid</SystematicName>
-<Xref>CAS:7298-99-9</Xref>
-<Xref>ChEBI:10696</Xref>
-<Xref>PDBHET:BHD</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 5 N 1 O 4</Formula>
-<Weight type="chemical">131.09</Weight>
-<Weight type="physical">131.021858</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0004">
-<Formula>C 0 H 0 N 0 O 1</Formula>
-<Weight type="chemical">16.00</Weight>
-<Weight type="physical">15.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yang, M.</Author>
-<Author>Ge, W.</Author>
-<Author>Chowdhury, R.</Author>
-<Author>Claridge, T.D.</Author>
-<Author>Kramer, H.B.</Author>
-<Author>Schmierer, B.</Author>
-<Author>McDonough, M.A.</Author>
-<Author>Gong, L.</Author>
-<Author>Kessler, B.M.</Author>
-<Author>Ratcliffe, P.J.</Author>
-<Author>Coleman, M.L.</Author>
-<Author>Schofield, C.J.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 286, 7648-7660, 2011</Citation>
-<Title>Asparagine and aspartate hydroxylation of the cytoskeletal ankyrin family is catalyzed by factor-inhibiting hypoxia-inducible factor.</Title>
-<Xref>DOI:10.1074/jbc.M110.193540</Xref>
-<Xref>PMID:21177872</Xref>
-<Note>mass spectrometric detection; (1)H-NMR and (13)C-NMR identification; X-ray diffraction, 2.20 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yang, M.</Author>
-<Author>Ge, W.</Author>
-<Author>Chowdhury, R.</Author>
-<Author>McDonough, M.A.</Author>
-<Author>Schofield, C.J.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, October 2010</Citation>
-<Description>Factor-inhibiting HIF (FIH) Q239H mutant in complex with Zn(II), NOG and Asp-substrate peptide (20-mer).</Description>
-<Xref>PDB:2XUM</Xref>
-<Note>X-ray diffraction, 2.20 angstroms</Note>
-</ReferenceBlock>
-<Comment>This diastereomeric form has been found in the ankyrin repeat domain of many proteins. For the (2S,3R)-diastereomer, see RESID:AA0027.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>hypoxia-inducible factor-asparagine dioxygenase (EC 1.14.11.30)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>D</SequenceSpec>
-<Xref>PSI-MOD:01919</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__(3s)-3-hydroxyaspartate__d">MOD_RES (3S)-3-hydroxyaspartate</Feature>
-</Features>
-<Image src="/images/AA0579.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0579.PDB" />
-</Entry>
-<Entry id="AA0580">
-<Header>
-<Code>AA0580</Code>
-<Dates>
-<CreationDate>31-Mar-2012</CreationDate>
-<StrucRevDate>31-Mar-2012</StrucRevDate>
-<TextChngDate>20-Apr-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>3-hydroxy-L-histidine</Name>
-<SystematicName>(2S)-2-amino-3-hydroxy-3-(1H-imidazol-4-yl)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 7 N 3 O 2</Formula>
-<Weight type="chemical">153.14</Weight>
-<Weight type="physical">153.053826</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0009">
-<Formula>C 0 H 0 N 0 O 1</Formula>
-<Weight type="chemical">16.00</Weight>
-<Weight type="physical">15.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Yang, M.</Author>
-<Author>Chowdhury, R.</Author>
-<Author>Ge, W.</Author>
-<Author>Hamed, R.B.</Author>
-<Author>McDonough, M.A.</Author>
-<Author>Claridge, T.D.</Author>
-<Author>Kessler, B.M.</Author>
-<Author>Cockman, M.E.</Author>
-<Author>Ratcliffe, P.J.</Author>
-<Author>Schofield, C.J.</Author>
-</Authors>
-<Citation>FEBS J. 278, 1086-1097, 2011</Citation>
-<Title>Factor-inhibiting hypoxia-inducible factor (FIH) catalyses the post-translational hydroxylation of histidinyl residues within ankyrin repeat domains.</Title>
-<Xref>DOI:10.1111/j.1742-4658.2011.08022.x</Xref>
-<Xref>PMID:21251231</Xref>
-<Note>mass spectrometric detection; (1)H-NMR identification; X-ray diffraction, 2.28 angstroms; the unmodified peptide was used in the crystallographic work</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Chowdhury, R.</Author>
-<Author>McDonough, M.A.</Author>
-<Author>Schofield, C.J.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, December 2010</Citation>
-<Description>Factor-inhibiting HIF-1 alpha in complex with tankyrase-2 (TNKS2) fragment peptide (21-mer).</Description>
-<Xref>PDB:2Y0I</Xref>
-<Note>X-ray diffraction, 2.28 angstroms</Note>
-</ReferenceBlock>
-<Comment>This modified histidine has been found in an ankyrin repeat domain in a position occupied by asparagine in homologous sequences. The diastereomeric form has not been determined.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptide-histidine beta-dioxygenase (EC 1.14.11.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>H</SequenceSpec>
-<Xref>PSI-MOD:01920</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__3-hydroxyhistidine__h">MOD_RES 3-hydroxyhistidine</Feature>
-</Features>
-<Image src="/images/AA0580.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0580.PDB" />
-</Entry>
-<Entry id="AA0581">
-<Header>
-<Code>AA0581</Code>
-<Dates>
-<CreationDate>31-Mar-2012</CreationDate>
-<StrucRevDate>13-Sep-2013</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-methionine (R)-sulfoxide</Name>
-<AlternateName>L-methionine (R)-S-oxide</AlternateName>
-<SystematicName>(2S)-2-amino-4-[(R)-methylsulfinyl]butanoic acid </SystematicName>
-<Xref>CAS:3226-66-2</Xref>
-<Xref>ChEBI:45764</Xref>
-<Xref>PDBHET:SME</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 9 N 1 O 2 S 1</Formula>
-<Weight type="chemical">147.19</Weight>
-<Weight type="physical">147.035400</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0013">
-<Formula>C 0 H 0 N 0 O 1 S 0</Formula>
-<Weight type="chemical">16.00</Weight>
-<Weight type="physical">15.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ghesquière, B.</Author>
-<Author>Jonckheere, V.</Author>
-<Author>Colaert, N.</Author>
-<Author>Van Durme, J.</Author>
-<Author>Timmerman, E.</Author>
-<Author>Goethals, M.</Author>
-<Author>Schymkowitz, J.</Author>
-<Author>Rousseau, F.</Author>
-<Author>Vandekerckhove, J.</Author>
-<Author>Gevaert, K.</Author>
-</Authors>
-<Citation>Mol. Cell. Proteomics 10, M110.006866, 2011</Citation>
-<Title>Redox proteomics of protein-bound methionine oxidation.</Title>
-<Xref>DOI:10.1074/mcp.M110.006866</Xref>
-<Xref>PMID:21406390</Xref>
-<Note>mass spectrometric and enzymatic analysis</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Hung, R.J.</Author>
-<Author>Pak, C.W.</Author>
-<Author>Terman, J.R.</Author>
-</Authors>
-<Citation>Science 334, 1710-1713, 2011</Citation>
-<Title>Direct redox regulation of F-actin assembly and disassembly by Mical.</Title>
-<Xref>DOI:10.1126/science.1211956</Xref>
-<Xref>PMID:22116028</Xref>
-<Note>mass spectrometric detection; directed mutation analysis; the stereochemistry was not determined; observation of a 64 Da neutral loss in the dioxidized peptide indicates that at least one of the methionine residues was probably an S-oxide</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lee, B.C.</Author>
-<Author>Péterfi, Z.</Author>
-<Author>Hoffmann, F.W.</Author>
-<Author>Moore, R.E.</Author>
-<Author>Kaya, A.</Author>
-<Author>Avanesov, A.</Author>
-<Author>Tarrago, L.</Author>
-<Author>Zhou, Y.</Author>
-<Author>Weerapana, E.</Author>
-<Author>Fomenko, D.E.</Author>
-<Author>Hoffmann, P.R.</Author>
-<Author>Gladyshev, V.N.</Author>
-</Authors>
-<Citation>Mol. Cell 51, 397-404, 2013</Citation>
-<Title>MsrB1 and MICALs Regulate Actin Assembly and Macrophage Function via Reversible Stereoselective Methionine Oxidation.</Title>
-<Xref>DOI:10.1016/j.molcel.2013.06.019</Xref>
-<Xref>PMID:23911929</Xref>
-<Note>it is established that the methionine sulfoxide residues of oxidized, and depolymerized, actin are stereoselctively reduced to methionine by the selenoenzyme methionine-R-sulfoxide reductase B1, and thus that the modified form is methionine (R)-sulfoxide</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Gruez, A.</Author>
-<Author>Libiad, M.</Author>
-<Author>Boschi-Muller, S.</Author>
-<Author>Branlant, G.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, April 2010</Citation>
-<Description>X-ray structure of free methionine-R-sulfoxide reductase from Neisseria meningitidis in complex with its substrate.</Description>
-<Xref>PDB:3MMH</Xref>
-<Note>X-ray diffraction, 1.25 angstroms; the free amino acid is modeled in the active site of the stereospecific methionine (R)-sulfoxide MsrB reductase</Note>
-</ReferenceBlock>
-<Comment>The S-oxide of methionine is a chiral center. The oxidized methionine in actin has been determined to be the (R)-sulfoxide.</Comment>
-<Comment>The methionine (R)-sulfoxides in actin can be reduced to methionine by methionine-R-sulfoxide reductase B1, MsrB1 (EC 1.8.4.12).</Comment>
-<GeneratingEnzyme>
-<EnzymeName>[F-actin]-L-methionine,NADPH:O2 S-oxidoreductase (EC 1.14.13.225)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>M</SequenceSpec>
-<Xref>PSI-MOD:00721</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__methionine (r)-sulfoxide__m">MOD_RES Methionine (R)-sulfoxide</Feature>
-<FeatureNote>
-<Feature type="UniProt" key="mod_res__methionine sulfoxide__m">MOD_RES Methionine sulfoxide</Feature>
-<Note>this UniProt feature is used when the stereochemistry has not been determined</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0581.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0581.PDB" />
-</Entry>
-<Entry id="AA0582">
-<Header>
-<Code>AA0582</Code>
-<Dates>
-<CreationDate>31-Mar-2012</CreationDate>
-<StrucRevDate>31-Mar-2012</StrucRevDate>
-<TextChngDate>31-Mar-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>3-methoxydehydroalanine</Name>
-<AlternateName>3-methoxydidehydroalanine</AlternateName>
-<SystematicName>2-amino-3-methoxyprop-2-enoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 5 N 1 O 2</Formula>
-<Weight type="chemical">99.09</Weight>
-<Weight type="physical">99.032028</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 1 H 0 N 0 O 0</Formula>
-<Weight type="chemical">12.01</Weight>
-<Weight type="physical">12.000000</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Mukai, A.</Author>
-<Author>Fukai, T.</Author>
-<Author>Hoshino, Y.</Author>
-<Author>Yazawa, K.</Author>
-<Author>Harada, K.-I.</Author>
-<Author>Mikami, Y.</Author>
-</Authors>
-<Citation>J. Antibiot. 62, 613-619, 2009</Citation>
-<Title>Nocardithiocin, a novel thiopeptide antibiotic, produced by pathogenic Nocardia pseudobrasiliensis IFM 0757.</Title>
-<Xref>DOI:10.1038/ja.2009.90</Xref>
-<Xref>PMID:19745839</Xref>
-<Note>the initials of K.-I. Harada in the PubMed citation are corrected</Note>
-</ReferenceBlock>
-<Comment>It has not been established whether the natural form is the Z or the E isomer. The Z isomer is shown.</Comment>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Condition>incidental to RESID:AA0242</Condition>
-<Xref>PSI-MOD:01922</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>methylated amino acid</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0582.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0582.PDB" />
-</Entry>
-<Entry id="AA0583">
-<Header>
-<Code>AA0583</Code>
-<Dates>
-<CreationDate>31-Mar-2012</CreationDate>
-<StrucRevDate>31-Mar-2012</StrucRevDate>
-<TextChngDate>31-Dec-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6-(L-aspartyl)-L-lysine</Name>
-<AlternateName>alpha-(N6-lysyl)aspartyl acid</AlternateName>
-<AlternateName>aspartyl N6-lysine</AlternateName>
-<AlternateName>N(epsilon)-(alpha-aspartyl)lysine</AlternateName>
-<SystematicName>(2S)-2-amino-6-([(2S)-2-amino-3-carboxypropanoyl]amino)hexanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 10 H 16 N 3 O 4</Formula>
-<Weight type="chemical">242.26</Weight>
-<Weight type="physical">242.114081</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0004 AA0012">
-<Formula>C 0 H -2 N 0 O -1</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Osička, R.</Author>
-<Author>Procházková, K.</Author>
-<Author>Šulc, M.</Author>
-<Author>Linhartová, I.</Author>
-<Author>Havlíček, V.</Author>
-<Author>Šebo, P.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 279, 24944-24956, 2004</Citation>
-<Title>A novel &quot;clip-and-link&quot; activity of repeat in toxin (RTX) proteins from gram-negative pathogens. Covalent protein cross-linking by an Asp-Lys isopeptide bond upon calcium-dependent processing at an Asp-Pro bond.</Title>
-<Xref>DOI:10.1074/jbc.M314013200</Xref>
-<Xref>PMID:15044436</Xref>
-<Note>chemical characterization and mass spectrometric identification; directed mutation analysis; it was not determined whether the cross-link was through the aspartyl C1 or C4 carboxyl, and both are probably formed, see also RESID:AA0294; the encoding of an author's name in the PubMed citation is corrected to UTF8</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Osipiuk, J.</Author>
-<Author>Mulligan, R.</Author>
-<Author>Bargassa, M.</Author>
-<Author>Hamilton, J.E.</Author>
-<Author>Cunningham, M.A.</Author>
-<Author>Joachimiak, A.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 287, 19452-19461, 2012</Citation>
-<Title>Characterization of member of DUF1888 protein family, self-cleaving and self-assembling endopeptidase.</Title>
-<Xref>DOI:10.1074/jbc.M112.358069</Xref>
-<Xref>PMID:22493430</Xref>
-<Note>X-ray diffraction, 1.57 angstroms; the cross-link is discussed and is annotated in the revised PDB entry</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Osipiuk, J.</Author>
-<Author>Mulligan, R.</Author>
-<Author>Collart, A.</Author>
-<Author>Joachimiak, A.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, May 2010</Citation>
-<Description>SO1698 protein, an aspartic peptidase from Shewanella oneidensis.</Description>
-<Xref>PDB:3N55</Xref>
-<Note>X-ray diffraction, 1.57 angstroms</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>D, K</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:01923</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked carboxyl end</Keyword>
-<Keyword>isopeptide bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__aspartyl lysine isopeptide (asp-lys) (interchain with k-__d">CROSSLNK Aspartyl lysine isopeptide (Asp-Lys) (interchain with K-...)</Feature>
-<Feature type="UniProt" key="crosslnk__aspartyl lysine isopeptide (lys-asp) (interchain with d-__k">CROSSLNK Aspartyl lysine isopeptide (Lys-Asp) (interchain with D-...)</Feature>
-</Features>
-<Image src="/images/AA0583.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0583.PDB" />
-</Entry>
-<Entry id="AA0584">
-<Header>
-<Code>AA0584</Code>
-<Dates>
-<CreationDate>31-Mar-2012</CreationDate>
-<StrucRevDate>31-Mar-2012</StrucRevDate>
-<TextChngDate>31-Mar-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-octanoyl-L-cysteine</Name>
-<AlternateName>2-amino-3-(octanoylthio)propanoic acid</AlternateName>
-<AlternateName>cysteine octanoate thioester</AlternateName>
-<SystematicName>(2S)-2-amino-3-(octanoylsulfanyl)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 11 H 19 N 1 O 2 S 1</Formula>
-<Weight type="chemical">229.34</Weight>
-<Weight type="physical">229.113650</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 8 H 14 N 0 O 1 S 0</Formula>
-<Weight type="chemical">126.20</Weight>
-<Weight type="physical">126.104465</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Jordan, S.W.</Author>
-<Author>Cronan Jr., J.E.</Author>
-</Authors>
-<Citation>J. Bacteriol. 185, 1582-1589, 2003</Citation>
-<Title>The Escherichia coli lipB gene encodes lipoyl (octanoyl)-acyl carrier protein:protein transferase.</Title>
-<Xref>DOI:10.1128/JB.185.5.1582-1589.2003</Xref>
-<Xref>PMID:12591875</Xref>
-<Note>identification of enzyme activity for the modification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Zhao, X.</Author>
-<Author>Miller, J.R.</Author>
-<Author>Cronan, J.E.</Author>
-</Authors>
-<Citation>Biochemistry 44, 16737-16746, 2005</Citation>
-<Title>The reaction of LipB, the octanoyl-[acyl carrier protein]:protein N-octanoyltransferase of lipoic acid synthesis, proceeds through an acyl-enzyme intermediate.</Title>
-<Xref>DOI:10.1021/bi051865y</Xref>
-<Xref>PMID:16342964</Xref>
-<Note>chemical characterization and mass spectrometric identification; directed mutation analysis</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>PSI-MOD:01924</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lipoprotein</Keyword>
-<Keyword>thioester bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="act_site__acyl-thioester intermediate__c">ACT_SITE Acyl-thioester intermediate</Feature>
-</Features>
-<Image src="/images/AA0584.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0584.PDB" />
-</Entry>
-<Entry id="AA0585">
-<Header>
-<Code>AA0585</Code>
-<Dates>
-<CreationDate>30-Jun-2012</CreationDate>
-<StrucRevDate>30-Jun-2012</StrucRevDate>
-<TextChngDate>30-Jun-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6-phospho-L-lysine</Name>
-<AlternateName>(2S)-2-azanyl-6-(phosphonoamino)hexanoic acid</AlternateName>
-<AlternateName>6-phospholysine</AlternateName>
-<AlternateName>N(6)-phosphonolysine</AlternateName>
-<AlternateName>N(epsilon)-phospholysine</AlternateName>
-<AlternateName>N(epsilon)-phosphonolysine</AlternateName>
-<AlternateName>N(epsilon)-phosphonyllysine</AlternateName>
-<AlternateName>N(epsilon)-phosphoryllysine</AlternateName>
-<SystematicName>(2S)-2-amino-6-(phosphonoamino)hexanoic acid</SystematicName>
-<Xref>CAS:14721-74-5</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 13 N 2 O 4 P 1</Formula>
-<Weight type="chemical">208.15</Weight>
-<Weight type="physical">208.061294</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 0 H 1 N 0 O 3 P 1</Formula>
-<Weight type="chemical">79.98</Weight>
-<Weight type="physical">79.966331</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Kowalewska, K.</Author>
-<Author>Stefanowicz, P.</Author>
-<Author>Ruman, T.</Author>
-<Author>Fraczyk, T.</Author>
-<Author>Rode, W.</Author>
-<Author>Szewczuk, Z.</Author>
-</Authors>
-<Citation>Biosci. Rep. 30, 433-443, 2010</Citation>
-<Title>Electron capture dissociation mass spectrometric analysis of lysine-phosphorylated peptides.</Title>
-<Xref>DOI:10.1042/BSR20090167</Xref>
-<Xref>PMID:20144148</Xref>
-<Note>mass spectrometric and (1)H-NMR analysis; chemical stability</Note>
-</ReferenceBlock>
-<Comment>N6-phospho-L-lysine hydrolyzes rapidly at acidic pH, but is more stable at neutral pH and below freezing.</Comment>
-<Comment>Although N6-phospho-L-lysine has been proposed to occur in histone H1, its occurrence has not been reported in a sequenced peptide.</Comment>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>PSI-MOD:01931</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0585.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0585.PDB" />
-</Entry>
-<Entry id="AA0586">
-<Header>
-<Code>AA0586</Code>
-<Dates>
-<CreationDate>30-Jun-2012</CreationDate>
-<StrucRevDate>30-Jun-2012</StrucRevDate>
-<TextChngDate>01-Mar-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-lysinonorleucine</Name>
-<AlternateName>(2S,2'S)-6,6'-iminobis(2-aminohexanoic acid)</AlternateName>
-<AlternateName>6-(N6-L-lysino)-L-norleucine</AlternateName>
-<AlternateName>lysinonorleucine</AlternateName>
-<AlternateName>lysinorleucine [misspelling]</AlternateName>
-<AlternateName>lysylnorleucine</AlternateName>
-<AlternateName>N6-[(5S)-5-amino-5-carboxypentyl]-L-lysine</AlternateName>
-<SystematicName>(2S)-2-amino-6-([(5S)-5-amino-5-carboxypentyl]amino)hexanoic acid</SystematicName>
-<Xref>CAS:25612-46-8</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 12 H 21 N 3 O 2</Formula>
-<Weight type="chemical">239.32</Weight>
-<Weight type="physical">239.163377</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012 AA0012">
-<Formula>C 0 H -3 N -1 O 0</Formula>
-<Weight type="chemical">-17.03</Weight>
-<Weight type="physical">-17.026549</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Franzblau, C.</Author>
-<Author>Sinex, F.M.</Author>
-<Author>Faris, B.</Author>
-<Author>Lampidis, R.</Author>
-</Authors>
-<Citation>Biochem. Biophys. Res. Commun. 21, 575-581, 1965</Citation>
-<Title>Identification of a new crosslinking amino acid in elastin.</Title>
-<Xref>DOI:10.1016/0006-291X(65)90524-3</Xref>
-<Xref>PMID:5879466</Xref>
-<Note>isolation of reduced form; chemical characterization and naming of lysinonorleucine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Franzblau, C.</Author>
-<Author>Faris, B.</Author>
-<Author>Papaioannou, R.</Author>
-</Authors>
-<Citation>Biochemistry 8, 2833-2837, 1969</Citation>
-<Title>Lysinonorleucine. A new amino acid from hydrolysates of elastin.</Title>
-<Xref>DOI:10.1021/bi00835a021</Xref>
-<Xref>PMID:5817620</Xref>
-<Note>mass spectrometric and chemical characterization of the reduced form; stereochemical determination</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lent, R.</Author>
-<Author>Franzblau, C.</Author>
-</Authors>
-<Citation>Biochem. Biophys. Res. Commun. 26, 43-50, 1967</Citation>
-<Title>Studies on the reduction of bovine elastin: evidence for the presence of Delta-6,7-dehydrolysinonorleucine.</Title>
-<Xref>DOI:10.1016/0006-291X(67)90250-1</Xref>
-<Xref>PMID:6030254</Xref>
-<Note>observation of the aldimine form</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bailey, A.J.</Author>
-<Author>Peach, C.M.</Author>
-</Authors>
-<Citation>Biochem. J. 121, 257-259, 1971</Citation>
-<Title>The chemistry of the collagen cross-links. The absence of reduction of dehydrolysinonorleucine and dehydrohydroxylysinonorleucine in vivo.</Title>
-<Xref>PMID:5117030</Xref>
-<Note>the non-reduced aldimine form is the predominant form in collagen, and in insoluble collagens there is less hydroxylation; the predominant form in elastin is the reduced lysinonorleucine</Note>
-</ReferenceBlock>
-<Comment>After the oxidation of a lysine to allysine (see RESID:AA0121), this cross-link forms spontaneously with a Schiff-base reaction. In this aleatoric modification two peptide chains may be crosslinked with the peptides contributing a lysine in either biosynthetic position.</Comment>
-<Comment>The lysines forming the cross-link may also be hydroxylated and glycosylated (see RESID:AA0028 and RESID:AA0153).</Comment>
-<GeneratingEnzyme>
-<EnzymeName>lysyl oxidase (EC 1.4.3.13)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>K, K</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Condition>incidental to RESID:AA0028</Condition>
-<Condition>secondary to RESID:AA0121</Condition>
-<Xref>PSI-MOD:01932</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>aleatoric crosslink</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0586.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0586.PDB" />
-</Entry>
-<Entry id="AA0587">
-<Header>
-<Code>AA0587</Code>
-<Dates>
-<CreationDate>30-Jun-2012</CreationDate>
-<StrucRevDate>30-Jun-2012</StrucRevDate>
-<TextChngDate>01-Mar-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>desmosine</Name>
-<AlternateName>6-[4-(4-amino-4-carboxybutyl)-3,5-bis(3-amino-3-carboxypropyl)pyridinio]norleucine</AlternateName>
-<SystematicName>4-[(4S)-4-amino-4-carboxybutyl]-1-[(5S)-5-amino-5-carboxypentyl]-3,5-bis[(3S)-3-amino-3-carboxypropyl]pyridinium</SystematicName>
-<Xref>CAS:11003-57-9</Xref>
-<Xref>ChEBI:37629</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 24 H 32 N 5 O 4</Formula>
-<FormalCharge>1+</FormalCharge>
-<Weight type="chemical">454.55</Weight>
-<Weight type="physical">454.244881</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012 AA0012 AA0012 AA0012">
-<Formula>C 0 H -16 N -3 O 0</Formula>
-<FormalCharge>1+</FormalCharge>
-<Weight type="chemical">-58.15</Weight>
-<Weight type="physical">-58.134971</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Partridge, S.M.</Author>
-<Author>Elsden, D.F.</Author>
-<Author>Thomas, J.</Author>
-</Authors>
-<Citation>Nature 197, 1297-1298, 1963</Citation>
-<Title>Constitution of the cross-linkages in elastin.</Title>
-<Xref>DOI:10.1038/1971297a0</Xref>
-<Xref>PMID:13941623</Xref>
-<Note>isolation; chemical characterization; determination of molecular weight and elemental composition; spectrographic characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Thomas, J.</Author>
-<Author>Elsden, D.F.</Author>
-<Author>Partridge, S.M.</Author>
-</Authors>
-<Citation>Nature 200, 651-652, 1963</Citation>
-<Title>Partial structure of two major degradation products from the cross-linkages in elastin.</Title>
-<Xref>DOI:10.1038/200651a0</Xref>
-<Xref>PMID:14109938</Xref>
-<Note>determination of molecular weight and elemental composition</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bedford, G.R.</Author>
-<Author>Katritzky, A.R.</Author>
-</Authors>
-<Citation>Nature 200, 652, 1963</Citation>
-<Title>Proton magnetic resonance spectra of degradation products from elastin.</Title>
-<Xref>DOI:10.1038/200652a0</Xref>
-<Xref>PMID:14109939</Xref>
-<Note>(1)H-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Partridge, S.M.</Author>
-<Author>Elsden, D.F.</Author>
-<Author>Thomas, J.</Author>
-<Author>Dorfman, A.</Author>
-<Author>Telser, A.</Author>
-<Author>Ho, P.L.</Author>
-</Authors>
-<Citation>Biochem. J. 93, 30C-33C, 1964</Citation>
-<Title>Biosynthesis of the desmosine and isodesmosine cross-bridges in elastin.</Title>
-<Xref>PMID:5839176</Xref>
-<Note>determination of molecular structure; radiolabeling; biosynthesis; the initials of P.-L. Ho in the PubMed citation are corrected</Note>
-</ReferenceBlock>
-<Comment>After the oxidation of three of the four lysines to allysine (see RESID:AA0121), this cross-link forms spontaneously with a Schiff-base reaction, and a series of one aldimine and two aldol condensation reactions. In this aleatoric modification up to four peptide chains may be crosslinked, with each peptide contributing a lysine potentially in any of the four biosynthetic positions. Isodesmosine is a structural isomer (see RESID:AA0588).</Comment>
-<Comment>Up to two of the lysines forming the cross-link may also be hydroxylated and glycosylated (see RESID:AA0028 and RESID:AA0153).</Comment>
-<GeneratingEnzyme>
-<EnzymeName>lysyl oxidase (EC 1.4.3.13)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>K, K, K, K</SequenceSpec>
-<Condition>cross-link 4</Condition>
-<Condition>incidental to RESID:AA0028</Condition>
-<Condition>secondary to RESID:AA0121</Condition>
-<Xref>PSI-MOD:01933</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>aleatoric crosslink</Keyword>
-<Keyword>pyridine ring</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0587.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0587.PDB" />
-</Entry>
-<Entry id="AA0588">
-<Header>
-<Code>AA0588</Code>
-<Dates>
-<CreationDate>30-Jun-2012</CreationDate>
-<StrucRevDate>30-Jun-2012</StrucRevDate>
-<TextChngDate>01-Mar-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>isodesmosine</Name>
-<AlternateName>6-[2-(4-amino-4-carboxybutyl)-3,5-bis(3-amino-3-carboxypropyl)pyridinio]norleucine</AlternateName>
-<SystematicName>2-[(4S)-4-amino-4-carboxybutyl]-1-[(5S)-5-amino-5-carboxypentyl]-3,5-bis[(3S)-3-amino-3-carboxypropyl]pyridinium</SystematicName>
-<Xref>CAS:991-01-5</Xref>
-<Xref>ChEBI:64366</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 24 H 32 N 5 O 4</Formula>
-<FormalCharge>1+</FormalCharge>
-<Weight type="chemical">454.55</Weight>
-<Weight type="physical">454.244881</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012 AA0012 AA0012 AA0012">
-<Formula>C 0 H -16 N -3 O 0</Formula>
-<FormalCharge>1+</FormalCharge>
-<Weight type="chemical">-58.15</Weight>
-<Weight type="physical">-58.134971</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Partridge, S.M.</Author>
-<Author>Elsden, D.F.</Author>
-<Author>Thomas, J.</Author>
-</Authors>
-<Citation>Nature 197, 1297-1298, 1963</Citation>
-<Title>Constitution of the cross-linkages in elastin.</Title>
-<Xref>DOI:10.1038/1971297a0</Xref>
-<Xref>PMID:13941623</Xref>
-<Note>isolation; chemical characterization; determination of molecular weight and elemental composition; spectrographic characterization</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Thomas, J.</Author>
-<Author>Elsden, D.F.</Author>
-<Author>Partridge, S.M.</Author>
-</Authors>
-<Citation>Nature 200, 651-652, 1963</Citation>
-<Title>Partial structure of two major degradation products from the cross-linkages in elastin.</Title>
-<Xref>DOI:10.1038/200651a0</Xref>
-<Xref>PMID:14109938</Xref>
-<Note>determination of molecular weight and elemental composition</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bedford, G.R.</Author>
-<Author>Katritzky, A.R.</Author>
-</Authors>
-<Citation>Nature 200, 652, 1963</Citation>
-<Title>Proton magnetic resonance spectra of degradation products from elastin.</Title>
-<Xref>DOI:10.1038/200652a0</Xref>
-<Xref>PMID:14109939</Xref>
-<Note>(1)H-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Partridge, S.M.</Author>
-<Author>Elsden, D.F.</Author>
-<Author>Thomas, J.</Author>
-<Author>Dorfman, A.</Author>
-<Author>Telser, A.</Author>
-<Author>Ho, P.L.</Author>
-</Authors>
-<Citation>Biochem. J. 93, 30C-33C, 1964</Citation>
-<Title>Biosynthesis of the desmosine and isodesmosine cross-bridges in elastin.</Title>
-<Xref>PMID:5839176</Xref>
-<Note>determination of molecular structure; radiolabeling; biosynthesis; the initials of P.-L. Ho in the PubMed citation are corrected</Note>
-</ReferenceBlock>
-<Comment>After the oxidation of three of the four lysines to allysine (see RESID:AA0121), this cross-link forms spontaneously with a Schiff-base reaction, and a series of one aldimine and two aldol condensation reactions. In this aleatoric modification up to four peptide chains may be crosslinked, with each peptide contributing a lysine potentially in any of the four biosynthetic positions. Desmosine is a structural isomer (see RESID:AA0587).</Comment>
-<Comment>Up to two of the lysines forming the cross-link may also be hydroxylated and glycosylated (see RESID:AA0028 and RESID:AA0153).</Comment>
-<GeneratingEnzyme>
-<EnzymeName>lysyl oxidase (EC 1.4.3.13)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>K, K, K, K</SequenceSpec>
-<Condition>cross-link 4</Condition>
-<Condition>incidental to RESID:AA0028</Condition>
-<Condition>secondary to RESID:AA0121</Condition>
-<Xref>PSI-MOD:01934</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>aleatoric crosslink</Keyword>
-<Keyword>pyridine ring</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0588.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0588.PDB" />
-</Entry>
-<Entry id="AA0589">
-<Header>
-<Code>AA0589</Code>
-<Dates>
-<CreationDate>30-Jun-2012</CreationDate>
-<StrucRevDate>30-Jun-2012</StrucRevDate>
-<TextChngDate>30-Jun-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-glucosyl-L-hydroxylysine</Name>
-<SystematicName>(D-glucopyranosyl)oxy-L-lysine</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 12 H 22 N 2 O 7</Formula>
-<Weight type="chemical">306.32</Weight>
-<Weight type="physical">306.142701</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 6 H 10 N 0 O 6</Formula>
-<Weight type="chemical">178.14</Weight>
-<Weight type="physical">178.047738</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Luther, K.B.</Author>
-<Author>Hülsmeier, A.J.</Author>
-<Author>Schegg, B.</Author>
-<Author>Deuber, S.A.</Author>
-<Author>Raoult, D.</Author>
-<Author>Hennet, T.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 286, 43701-43709, 2011</Citation>
-<Title>Mimivirus collagen is modified by bifunctional lysyl hydroxylase and glycosyltransferase enzyme.</Title>
-<Xref>DOI:10.1074/jbc.M111.309096</Xref>
-<Xref>PMID:22045808</Xref>
-<Note>biosynthesis; cloning, expression and directed mutation analysis of the enzyme</Note>
-</ReferenceBlock>
-<Comment>The mimivirus enzyme is bifunctional and carries out both hydroxylation and glucosylation. Neither the regiospecificity nor stereospecificity of the hydroxylation, nor the anomeric specificity of the glucosylation have been determined.</Comment>
-<Comment>The 5-hydroxy, beta anomeric form is shown.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>lysine dioxygenase (EC 1.14.11.-)</EnzymeName>
-<EnzymeName>hydroxylysine glucosyltransferase (EC 2.4.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>PSI-MOD:01935</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0589.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0589.PDB" />
-</Entry>
-<Entry id="AA0590">
-<Header>
-<Code>AA0590</Code>
-<Dates>
-<CreationDate>30-Jun-2012</CreationDate>
-<StrucRevDate>30-Jun-2012</StrucRevDate>
-<TextChngDate>30-Jun-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6-oleoyl-L-lysine</Name>
-<AlternateName>N6-[(9Z)-1-oxo-9-octadecenyl]lysine</AlternateName>
-<SystematicName>(2S)-2-amino-6-([(9Z)-octadec-9-enoyl]amino)hexanoic acid</SystematicName>
-<Xref>CAS:23499-75-4</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 24 H 44 N 2 O 2</Formula>
-<Weight type="chemical">392.63</Weight>
-<Weight type="physical">392.340279</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 18 H 32 N 0 O 1</Formula>
-<Weight type="chemical">264.45</Weight>
-<Weight type="physical">264.245316</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Schey, K.L.</Author>
-<Author>Gutierrez, D.B.</Author>
-<Author>Wang, Z.</Author>
-<Author>Wei, J.</Author>
-<Author>Grey, A.C.</Author>
-</Authors>
-<Citation>Biochemistry 49, 9858-9865, 2010</Citation>
-<Title>Novel fatty acid acylation of lens integral membrane protein aquaporin-0.</Title>
-<Xref>DOI:10.1021/bi101415w</Xref>
-<Xref>PMID:20942504</Xref>
-<Note>mass spectrometric detection</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>peptidyl-lysine N6-oleoyltransferase (EC 2.3.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>PSI-MOD:01936</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lipoprotein</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0590.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0590.PDB" />
-</Entry>
-<Entry id="AA0591">
-<Header>
-<Code>AA0591</Code>
-<Dates>
-<CreationDate>30-Jun-2012</CreationDate>
-<StrucRevDate>30-Jun-2012</StrucRevDate>
-<TextChngDate>30-Jun-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N-palmitoyl-L-methionine</Name>
-<AlternateName>2-(hexadecanamido)-4-(methylsulfanyl)butanoic acid</AlternateName>
-<AlternateName>N-(1-oxohexadecyl)methionine</AlternateName>
-<SystematicName>(2S)-2-(hexadecanoylamino)-4-(methylsulfanyl)butanoic acid</SystematicName>
-<Xref>CAS:36416-81-6</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 21 H 40 N 1 O 2 S 1</Formula>
-<Weight type="chemical">370.62</Weight>
-<Weight type="physical">370.277976</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0013">
-<Formula>C 16 H 30 N 0 O 1 S 0</Formula>
-<Weight type="chemical">238.41</Weight>
-<Weight type="physical">238.229666</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Schey, K.L.</Author>
-<Author>Gutierrez, D.B.</Author>
-<Author>Wang, Z.</Author>
-<Author>Wei, J.</Author>
-<Author>Grey, A.C.</Author>
-</Authors>
-<Citation>Biochemistry 49, 9858-9865, 2010</Citation>
-<Title>Novel fatty acid acylation of lens integral membrane protein aquaporin-0.</Title>
-<Xref>DOI:10.1021/bi101415w</Xref>
-<Xref>PMID:20942504</Xref>
-<Note>mass spectrometric detection</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>methionylpeptide N-palmitoyltransferase (EC 2.3.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>M</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>PSI-MOD:01937</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-<Keyword>lipoprotein</Keyword>
-<Keyword>palmitoylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="lipid__n-palmitoyl methionine__m">LIPID N-palmitoyl methionine</Feature>
-</Features>
-<Image src="/images/AA0591.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0591.PDB" />
-</Entry>
-<Entry id="AA0592">
-<Header>
-<Code>AA0592</Code>
-<Dates>
-<CreationDate>30-Jun-2012</CreationDate>
-<StrucRevDate>30-Jun-2012</StrucRevDate>
-<TextChngDate>30-Jun-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>2-(2-aminosuccinimidyl)-3-sulfanylpropanoic acid</Name>
-<AlternateName>aspartimide cysteine</AlternateName>
-<SystematicName>(2R)-2-[(3S)-3-amino-2,5-dioxopyrrolidin-1-yl]-3-sulfanylpropanoic acid</SystematicName>
-<Xref>PDBHET:SIC</Xref>
-<Xref>PDBHET:SNN</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 8 N 2 O 3 S 1</Formula>
-<Weight type="chemical">200.21</Weight>
-<Weight type="physical">200.025563</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0003 AA0005" label="ASN">
-<Formula>C 0 H -3 N -1 O 0 S 0</Formula>
-<Weight type="chemical">-17.03</Weight>
-<Weight type="physical">-17.026549</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0004 AA0005" label="ASP">
-<Formula>C 0 H -2 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bonanno, J.B.</Author>
-<Author>Freeman, J.</Author>
-<Author>Bain, K.T.</Author>
-<Author>Zhang, F.</Author>
-<Author>Ozyurt, S.</Author>
-<Author>Smith, D.</Author>
-<Author>Wasserman, S.</Author>
-<Author>Sauder, J.M.</Author>
-<Author>Burley, S.K.</Author>
-<Author>Almo, S.C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, June 2008</Citation>
-<Description>Crystal structure of an enolase protein from the environmental genome shotgun sequencing of the Sargasso Sea.</Description>
-<Xref>PDB:3DIP</Xref>
-<Note>X-ray diffraction, 2.50 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Vetting, M.W.</Author>
-<Author>Bouvier, J.T.</Author>
-<Author>Toro, R.</Author>
-<Author>Bhosle, R.</Author>
-<Author>Al Obaidi, N.F.</Author>
-<Author>Morisco, L.L.</Author>
-<Author>Wasserman, S.R.</Author>
-<Author>Sojitra, S.</Author>
-<Author>Imker, H.J.</Author>
-<Author>Gerlt, J.A.</Author>
-<Author>Almo, S.C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, February 2012</Citation>
-<Description>Crystal structure of an enolase (Mandelate racemase subgroup, Target EFI-502086) from Agrobacterium tumefaciens, with a succinimide residue.</Description>
-<Xref>PDB:4DX3</Xref>
-<Note>X-ray diffraction, 1.65 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Vetting, M.W.</Author>
-<Author>Bouvier, J.T.</Author>
-<Author>Toro, R.</Author>
-<Author>Bhosle, R.</Author>
-<Author>Al Obaidi, N.F.</Author>
-<Author>Morisco, L.L.</Author>
-<Author>Wasserman, S.R.</Author>
-<Author>Sojitra, S.</Author>
-<Author>Imker, H.J.</Author>
-<Author>Gerlt, J.A.</Author>
-<Author>Almo, S.C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, February 2012</Citation>
-<Description>Crystal structure of an enolase (Mandelate racemase subgroup, target EFI-502086) from Agrobacterium tumefaciens, with a succinimide residue, Na and phosphate.</Description>
-<Xref>PDB:4DXK</Xref>
-<Note>X-ray diffraction, 1.25 angstroms</Note>
-</ReferenceBlock>
-<Comment>This cross-link is formed by the condensation of an aspartic acid or asparagine residue with the alpha-amido of the following residue.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode link="ASN">
-<SequenceSpec>C, N</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Xref>PSI-MOD:01938</Xref>
-</SequenceCode>
-<SequenceCode link="ASP">
-<SequenceSpec>C, D</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Xref>PSI-MOD:01939</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>succinimide ring</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0592.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0592.PDB" />
-</Entry>
-<Entry id="AA0593">
-<Header>
-<Code>AA0593</Code>
-<Dates>
-<CreationDate>30-Jun-2012</CreationDate>
-<StrucRevDate>30-Jun-2012</StrucRevDate>
-<TextChngDate>30-Jun-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>2-(2-aminosuccinimidyl)pentanedioic acid</Name>
-<AlternateName>aspartimide glutamic acid</AlternateName>
-<SystematicName>(4S)-4-[(3S)-3-amino-2,5-dioxopyrrolidin-1-yl]-5-oxopentanoic acid</SystematicName>
-<Xref>PDBHET:SNN</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 10 N 2 O 5</Formula>
-<Weight type="chemical">226.19</Weight>
-<Weight type="physical">226.058971</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0003 AA0006" label="ASN">
-<Formula>C 0 H -3 N -1 O 0</Formula>
-<Weight type="chemical">-17.03</Weight>
-<Weight type="physical">-17.026549</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0004 AA0006" label="ASP">
-<Formula>C 0 H -2 N 0 O -1</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lokanath, N.K.</Author>
-<Author>Kunishima, N.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, June 2004</Citation>
-<Description>Crystal structure of PH1346 protein from Pyrococcus horikoshii.</Description>
-<Xref>PDB:1WL8</Xref>
-<Note>X-ray diffraction, 1.45 angstroms</Note>
-</ReferenceBlock>
-<Comment>This cross-link is formed by the condensation of an aspartic acid or asparagine residue with the alpha-amido of the following residue.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode link="ASN">
-<SequenceSpec>E, N</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Xref>PSI-MOD:01940</Xref>
-</SequenceCode>
-<SequenceCode link="ASP">
-<SequenceSpec>D, E</SequenceSpec>
-<Condition>cross-link 1</Condition>
-<Xref>PSI-MOD:01941</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>succinimide ring</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0593.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0593.PDB" />
-</Entry>
-<Entry id="AA0594">
-<Header>
-<Code>AA0594</Code>
-<Dates>
-<CreationDate>24-Aug-2012</CreationDate>
-<StrucRevDate>24-Aug-2012</StrucRevDate>
-<TextChngDate>31-May-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>labionin</Name>
-<AlternateName>(2S,4S,8R)-2,4,8-triamino-4-carboxy-6-thianonanedioic acid</AlternateName>
-<AlternateName>(2S,4S,8R)-labionin</AlternateName>
-<SystematicName>(2S,4S)-2,4-diamino-2-[([(2R)-2-amino-2-carboxyethyl]sulfanyl)methyl]pentanedioic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 11 N 3 O 3 S 1</Formula>
-<Weight type="chemical">241.26</Weight>
-<Weight type="physical">241.052112</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0016 AA0016">
-<Formula>C 0 H -4 N 0 O -2 S 0</Formula>
-<Weight type="chemical">-36.03</Weight>
-<Weight type="physical">-36.021129</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Meindl, K.</Author>
-<Author>Schmiederer, T.</Author>
-<Author>Schneider, K.</Author>
-<Author>Reicke, A.</Author>
-<Author>Butz, D.</Author>
-<Author>Keller, S.</Author>
-<Author>Gühring, H.</Author>
-<Author>Vértesy, L.</Author>
-<Author>Wink, J.</Author>
-<Author>Hoffmann, H.</Author>
-<Author>Brönstrup, M.</Author>
-<Author>Sheldrick, G.M.</Author>
-<Author>Süssmuth, R.D.</Author>
-</Authors>
-<Citation>Angew. Chem. Int. Ed. Engl. 49, 1151-1154, 2010</Citation>
-<Title>Labyrinthopeptins: a new class of carbacyclic lantibiotics.</Title>
-<Xref>DOI:10.1002/anie.200905773</Xref>
-<Xref>PMID:20082397</Xref>
-<Note>mass spectrometric characterization and chemical characterization; gene sequence for the encoded peptide; X-ray diffraction, 1.0 angstroms; structure in Cambridge Crystallographic Data Center (721326); naming</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Pesic, A.</Author>
-<Author>Henkel, M.</Author>
-<Author>Süssmuth, R.D.</Author>
-</Authors>
-<Citation>Chem. Commun. (Camb.) 47, 7401-7403, 2011</Citation>
-<Title>Identification of the amino acid labionin and its desulfurised derivative in the type-III lantibiotic LabA2 by means of GC/MS.</Title>
-<Xref>DOI:10.1039/c1cc11573a</Xref>
-<Xref>PMID:21603709</Xref>
-<Note>mass spectrometric identification</Note>
-</ReferenceBlock>
-<Comment>This three residue cross-link modification includes both a thioether bond and an alpha-linked carbon-carbon bond.</Comment>
-<SequenceCode>
-<SequenceSpec>C, S, S</SequenceSpec>
-<Condition>cross-link 3</Condition>
-<Xref>PSI-MOD:01948</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lanthionine</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="crosslnk__labionin (ser-ser) (with c-__s__s">CROSSLNK Labionin (Ser-Ser) (with C-...)</Feature>
-<Feature type="UniProt" key="crosslnk__labionin (ser-cys) (with s-__s__c">CROSSLNK Labionin (Ser-Cys) (with S-...)</Feature>
-</Features>
-<Image src="/images/AA0594.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0594.PDB" />
-</Entry>
-<Entry id="AA0595">
-<Header>
-<Code>AA0595</Code>
-<Dates>
-<CreationDate>24-Aug-2012</CreationDate>
-<StrucRevDate>24-Aug-2012</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>coelenterazine</Name>
-<AlternateName>Oplophorus luciferin</AlternateName>
-<SystematicName>8-benzyl-2-(4-hydroxybenzyl)-6-(4-hydroxyphenyl)imidazo[1,2-a]pyrazin-3(7H)-one</SystematicName>
-<Xref>CAS:55779-48-1</Xref>
-<Xref>ChEBI:2311</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 26 H 21 N 3 O 3</Formula>
-<Weight type="chemical">423.47</Weight>
-<Weight type="physical">423.158292</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0014 AA0019 AA0019">
-<Formula>C -1 H -8 N 0 O -3</Formula>
-<Weight type="chemical">-68.07</Weight>
-<Weight type="physical">-68.047344</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ward, W.W.</Author>
-<Author>Chalfie, M.</Author>
-</Authors>
-<Citation type="submission">submitted to the United States Patent Office, 21 April 1998</Citation>
-<Description>Expression of a gene for a modified green-fluorescent protein.</Description>
-<Xref>USPTO:US5741668</Xref>
-<Note>a claim of autocatalytic production of coelenterazine from a green fluorescent protein with a modified FYYG sequence has not been confirmed in a subsequent publication</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Head, J.F.</Author>
-<Author>Inouye, S.</Author>
-<Author>Teranishi, K.</Author>
-<Author>Shimomura, O.</Author>
-</Authors>
-<Citation>Nature 405, 372-376, 2000</Citation>
-<Title>The crystal structure of the photoprotein aequorin at 2.3 A resolution.</Title>
-<Xref>DOI:10.1038/35012659</Xref>
-<Xref>PMID:10830969</Xref>
-<Note>X-ray diffraction, 2.3 angstroms; contains the activated form colenterazine-2-hydroperoxide</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Head, J.F.</Author>
-<Author>Inouye, S.</Author>
-<Author>Teranishi, K.</Author>
-<Author>Shimomura, O.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, February 2000</Citation>
-<Description>Crystal structure of aequorin.</Description>
-<Xref>PDB:1EJ3</Xref>
-<Note>X-ray diffraction, 2.3 angstroms; contains the activated form colenterazine-2-hydroperoxide</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Haddock, S.H.</Author>
-<Author>Rivers, T.J.</Author>
-<Author>Robison, B.H.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 98, 11148-11151, 2001</Citation>
-<Title>Can coelenterates make coelenterazine? Dietary requirement for luciferin in cnidarian bioluminescence.</Title>
-<Xref>DOI:10.1073/pnas.201329798</Xref>
-<Xref>PMID:11572972</Xref>
-<Note>coelenterates cannot biosynthesize coelenterazine and acquire it by dietary intake</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Oba, Y.</Author>
-<Author>Kato, S.</Author>
-<Author>Ojika, M.</Author>
-<Author>Inouye, S.</Author>
-</Authors>
-<Citation>Biochem. Biophys. Res. Commun. 390, 684-688, 2009</Citation>
-<Title>Biosynthesis of coelenterazine in the deep-sea copepod, Metridia pacifica.</Title>
-<Xref>DOI:10.1016/j.bbrc.2009.10.028</Xref>
-<Xref>PMID:19833098</Xref>
-<Note>radiolabeling experiments establish that the coelenterazine is constucted from one molecule of phenylalanine and two of tyrosine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Francis, W.R.</Author>
-<Author>Shaner, N.C.</Author>
-<Author>Christianson, L.M.</Author>
-<Author>Powers, M.L.</Author>
-<Author>Haddock, S.H.</Author>
-</Authors>
-<Citation>PLoS ONE 10, e0128742, 2015</Citation>
-<Title>Occurrence of Isopenicillin-N-Synthase Homologs in Bioluminescent Ctenophores and Implications for Coelenterazine Biosynthesis.</Title>
-<Xref>DOI:10.1371/journal.pone.0128742</Xref>
-<Xref>PMID:26125183</Xref>
-<Note>candidate genes for coelenterazine precursors, found in luminous ctenophore species and not in non-luminous species, have Phe-Tyr-Tyr at their C-terminus and are conserved non-heme iron oxidases similar to isopenicillin-N-synthase</Note>
-</ReferenceBlock>
-<Comment>The structure of the amino acid components of coelenterazine suggest that it is biosynthesized from a phenylalanyl-tyrosyl-tyrosine peptide.</Comment>
-<Comment>This entry presents coelenterazine as a modification produced by the cross-linking of a tripeptide precursor. For coelenterazine as a heterogen cross-linked to a cysteine see RESID:AA0526.</Comment>
-<SequenceCode>
-<SequenceSpec>F, Y, Y</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Condition>carboxyl-terminal</Condition>
-<Condition>cross-link 3</Condition>
-<Xref>PSI-MOD:01949</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-<Keyword>blocked carboxyl end</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0595.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0595.PDB" />
-</Entry>
-<Entry id="AA0596">
-<Header>
-<Code>AA0596</Code>
-<Dates>
-<CreationDate>31-Dec-2012</CreationDate>
-<StrucRevDate>31-Dec-2012</StrucRevDate>
-<TextChngDate>31-Dec-2012</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-isoglutamyl histamine</Name>
-<AlternateName>(gamma-glutamyl)histamine</AlternateName>
-<SystematicName>(2S)-2-amino-5-([2-(1H-imidazol-5-yl)ethyl]amino)-5-oxopentanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 10 H 14 N 4 O 2</Formula>
-<Weight type="chemical">222.25</Weight>
-<Weight type="physical">222.111676</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0007">
-<Formula>C 5 H 6 N 2 O 0</Formula>
-<Weight type="chemical">94.12</Weight>
-<Weight type="physical">94.053098</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Vowinckel, J.</Author>
-<Author>Stahlberg, S.</Author>
-<Author>Paulmann, N.</Author>
-<Author>Bluemlein, K.</Author>
-<Author>Grohmann, M.</Author>
-<Author>Ralser, M.</Author>
-<Author>Walther, D.J.</Author>
-</Authors>
-<Citation>FEBS Lett. 586, 3819-3824, 2012</Citation>
-<Title>Histaminylation of glutamine residues is a novel posttranslational modification implicated in G-protein signaling.</Title>
-<Xref>DOI:10.1016/j.febslet.2012.09.027</Xref>
-<Xref>PMID:23022564</Xref>
-<Note>mass spectrometric identification</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>protein-glutamine gamma-glutamyltransferase (EC 2.3.2.13)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>Q</SequenceSpec>
-<Xref>PSI-MOD:01950</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0596.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0596.PDB" />
-</Entry>
-<Entry id="AA0597">
-<Header>
-<Code>AA0597</Code>
-<Dates>
-<CreationDate>31-Dec-2012</CreationDate>
-<StrucRevDate>31-Dec-2012</StrucRevDate>
-<TextChngDate>31-May-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-(L-isoglutamyl)-L-serine</Name>
-<AlternateName>O(beta)-(gamma-glutamyl)serine</AlternateName>
-<AlternateName>O3-(isoglutamyl)-serine</AlternateName>
-<SystematicName>(2S)-2-amino-5-[(2S)-2-amino-2-carboxyethoxy]-5-oxopentanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 8 H 10 N 2 O 4</Formula>
-<Weight type="chemical">198.18</Weight>
-<Weight type="physical">198.064057</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0006 AA0016" label="ESX">
-<Formula>C 0 H -2 N 0 O -1</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<CorrectionBlock uids="AA0007 AA0016" label="QSX">
-<Formula>C 0 H -3 N -1 O 0</Formula>
-<Weight type="chemical">-17.03</Weight>
-<Weight type="physical">-17.026549</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ishitsuka, M.O.</Author>
-<Author>Kusumi, T.</Author>
-<Author>Kakisawa, H.</Author>
-<Author>Kaya, K.</Author>
-<Author>Watanabe, M.M.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 112, 8180-8182, 1990</Citation>
-<Title>Microviridin. A novel tricyclic depsipeptide from the toxic cyanobacterium Microcystis viridis.</Title>
-<Xref>DOI:10.1021/ja00178a060</Xref>
-<Note>amino acid composition; (1)H-NMR and (13)C-NMR identification; chemical characterization of the ester cross-links</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Philmus, B.</Author>
-<Author>Christiansen, G.</Author>
-<Author>Yoshida, W.Y.</Author>
-<Author>Hemscheidt, T.K.</Author>
-</Authors>
-<Citation>Chembiochem 9, 3066-3073, 2008</Citation>
-<Title>Post-translational modification in microviridin biosynthesis.</Title>
-<Xref>DOI:10.1002/cbic.200800560</Xref>
-<Xref>PMID:19035375</Xref>
-<Note>(1)H-NMR and (13)C-NMR analysis; mass spectrometric and chemical characterization; directed mutation analysis; gene sequence for the encoded peptide</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Abdul Ajees, A.</Author>
-<Author>Gunasekaran, K.</Author>
-<Author>Volanakis, J.E.</Author>
-<Author>Narayana, S.V.</Author>
-<Author>Kotwal, G.J.</Author>
-<Author>Murthy, H.M.</Author>
-</Authors>
-<Citation>Nature 444, 221-225, 2006</Citation>
-<Title>The structure of complement C3b provides insights into complement activation and regulation.</Title>
-<Xref>DOI:10.1038/nature05258</Xref>
-<Xref>PMID:17051152</Xref>
-<Note>X-ray diffraction, 2.26 angstroms; N-acetyl-L-threonine is the model substrate</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Abdul Ajees, A.</Author>
-<Author>Gunasekaran, K.</Author>
-<Author>Volanakis, J.E.</Author>
-<Author>Narayana, S.V.</Author>
-<Author>Kotwal, G.J.</Author>
-<Author>Murthy, H.M.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, July 2006</Citation>
-<Description>Structure of complement C3B: Insights into complement activation and regulation.</Description>
-<Xref>PDB:2HR0</Xref>
-<Note>X-ray diffraction, 2.26 angstroms; N-acetyl-L-threonine is the model substrate</Note>
-</ReferenceBlock>
-<Comment>The ester cross-link of glutamate with serine is formed by an RimK related enzyme using ATP.</Comment>
-<Comment>The formation of an ester cross-link between serine residues of target proteins and complement C3 and C4 glutamine residues occurs autocatalytically after C3 and C4 form internal intermediate thioester cross-links with the liberation of ammonia.</Comment>
-<GeneratingEnzyme>
-<EnzymeName link="ESX">peptidyl-threonine--peptidyl-aspartate ligase MvdD (EC 6.1.2.-)</EnzymeName>
-<EnzymeName link="QSX">autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode link="ESX">
-<SequenceSpec>E, S</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:00953</Xref>
-</SequenceCode>
-<SequenceCode link="QSX">
-<SequenceSpec>Q, S</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:01951</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<Feature type="UniProt" key="crosslnk__isoglutamyl serine ester (ser-glu)__s__e" link="ESX">CROSSLNK isoglutamyl serine ester (Ser-Glu)</Feature>
-</Features>
-<Image src="/images/AA0597.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0597.PDB" />
-</Entry>
-<Entry id="AA0599">
-<Header>
-<Code>AA0599</Code>
-<Dates>
-<CreationDate>31-Dec-2012</CreationDate>
-<StrucRevDate>31-Dec-2012</StrucRevDate>
-<TextChngDate>31-Mar-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>tetrakis-L-cysteinyl tetrairon octanitrosyl</Name>
-<SystematicName>tetrakis(mu3-cysteinato-kappa(3)S)-octanitrosyl-1kappa(2)N,2kappa(2)N,3kappa(2),4kappa(2)N-tetrahedro-tetrairon</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 12 Fe 4 H 16 N 12 O 12 S 4</Formula>
-<Weight type="chemical">871.95</Weight>
-<Weight type="physical">871.729098</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005 AA0005 AA0005">
-<Formula>C 0 Fe 4 H -4 N 8 O 8 S 0</Formula>
-<Weight type="chemical">459.40</Weight>
-<Weight type="physical">459.692359</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Crack, J.C.</Author>
-<Author>Smith, L.J.</Author>
-<Author>Stapleton, M.R.</Author>
-<Author>Peck, J.</Author>
-<Author>Watmough, N.J.</Author>
-<Author>Buttner, M.J.</Author>
-<Author>Buxton, R.S.</Author>
-<Author>Green, J.</Author>
-<Author>Oganesyan, V.S.</Author>
-<Author>Thomson, A.J.</Author>
-<Author>Le Brun, N.E.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 133, 1112-1121, 2011</Citation>
-<Title>Mechanistic insight into the nitrosylation of the [4Fe-4S] cluster of WhiB-like proteins.</Title>
-<Xref>DOI:10.1021/ja109581t</Xref>
-<Xref>PMID:21182249</Xref>
-<Note>spectrographic characterization</Note>
-</ReferenceBlock>
-<Comment>It has been proposed that in the WhiD protein of Streptomyces coelicolor and Mycobacterium this cluster is rapidly and specifically produced by nitrosylation of a tetrakis-L-cysteinyl tetrairon tetrasulfide cluster. See RESID:AA0140.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C, C, C, C</SequenceSpec>
-<Condition>cross-link 4</Condition>
-<Xref>PSI-MOD:01953</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>iron</Keyword>
-<Keyword>metalloprotein</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0599.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0599.PDB" />
-</Entry>
-<Entry id="AA0600">
-<Header>
-<Code>AA0600</Code>
-<Dates>
-<CreationDate>01-Mar-2013</CreationDate>
-<StrucRevDate>01-Mar-2013</StrucRevDate>
-<TextChngDate>01-Mar-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>L-alaninato bis-L-aspartato tris-L-glutamato L-histidino calcium tetramanganese pentoxide</Name>
-<AlternateName>4Mn-Ca-5O cluster</AlternateName>
-<AlternateName>photosystem II catalytic cluster</AlternateName>
-<SystematicName>mu2-alaninato-1kappaO(1),3kappaO(1')-mu2-aspartato-1kappaO(4),5kappaO(4')-mu2-aspartato-2kappaO(4),3kappaO(4')-mu2-glutamato-3kappaO(5),4kappaO(5')-mu2-glutamato-4kappaO(5),5kappaO(5')-mu-glutamato-2kappaO(5)-mu-histidino-2kappaN(tau)-mu4-oxido-1:2:4:5kappa(4)O-tri-mu3-oxido-1:2:3kappa(3)O;1:3:4kappa(3)O;2:3:4kappa(3)O;mu-oxido-4:5kappa(2)O-calciumtetramanganese</SystematicName>
-<Xref>PDBHET:OEX</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 32 Ca 1 H 38 Mn 4 N 9 O 23</Formula>
-<Weight type="chemical">1176.53</Weight>
-<Weight type="physical">1175.922825</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0001 AA0004 AA0004 AA0006 AA0006 AA0006 AA0009">
-<Formula>C 0 Ca 1 H -6 Mn 4 N 0 O 5</Formula>
-<Weight type="chemical">333.78</Weight>
-<Weight type="physical">333.642394</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Umena, Y.</Author>
-<Author>Kawakami, K.</Author>
-<Author>Shen, J.R.</Author>
-<Author>Kamiya, N.</Author>
-</Authors>
-<Citation>Nature 473, 55-60, 2011</Citation>
-<Title>Crystal structure of oxygen-evolving photosystem II at a resolution of 1.9 Å.</Title>
-<Xref>DOI:10.1038/nature09913</Xref>
-<Xref>PMID:21499260</Xref>
-<Note>X-ray diffraction, 1.9 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Umena, Y.</Author>
-<Author>Kawakami, K.</Author>
-<Author>Shen, J.-R.</Author>
-<Author>Kamiya, N.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, October 2012</Citation>
-<Description>Crystal structure of oxygen-evolving photosystem II at 1.9 angstrom resolution.</Description>
-<Xref>PDB:3ARC</Xref>
-<Note>X-ray diffraction, 1.90 angstroms</Note>
-</ReferenceBlock>
-<Comment>The metal cluster consists of a three-manganese, one-calcium, four-oxygen cubane with a cubane oxygen that ligates the calcium also ligating a fourth manganese, and a fifth oxygen that ligates the fourth manganese and a cubane manganese. Additionally but not shown in the model, one omega amino group of an arginine donates hydrogen bonds to two cubane oxygens, and the tele-nitrogen of a histidine donates a hydrogen bond to another cubane oxygen.</Comment>
-<Comment>The reactive center for converting several water molecules to dioxygen may be between the calcium and the fourth manganese where electron density was modeled as bicarbonate and chloride ions.</Comment>
-<Comment>The formal charge is uncertain.</Comment>
-<SequenceCode>
-<SequenceSpec>A, D, D, E, E, E, H</SequenceSpec>
-<Condition>carboxyl-terminal</Condition>
-<Condition>cross-link 7</Condition>
-<Xref>PSI-MOD:01955</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>calcium</Keyword>
-<Keyword>manganese</Keyword>
-<Keyword>metalloprotein</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0600.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0600.PDB" />
-</Entry>
-<Entry id="AA0601">
-<Header>
-<Code>AA0601</Code>
-<Dates>
-<CreationDate>01-Mar-2013</CreationDate>
-<StrucRevDate>01-Mar-2013</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>(3R)-3-hydroxy-L-arginine</Name>
-<AlternateName>2-amino-5-(carbamimidamido)-3-hydroxypentanoic acid [tautomer]</AlternateName>
-<AlternateName>2-amino-5-guanidino-3-hydroxypentanoic acid</AlternateName>
-<AlternateName>2-amino-5-[(aminoiminomethyl)amino]-3-hydroxypentanoic acid [tautomer]</AlternateName>
-<AlternateName>beta-hydroxyarginine</AlternateName>
-<AlternateName>C(beta)-hydroxyarginine</AlternateName>
-<SystematicName>(2S,3R)-2-amino-5-[(diaminomethylidene)amino]-3-hydroxypentanoic acid</SystematicName>
-<Xref>ChEBI:29965</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 12 N 4 O 2</Formula>
-<Weight type="chemical">172.19</Weight>
-<Weight type="physical">172.096026</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0002">
-<Formula>C 0 H 0 N 0 O 1</Formula>
-<Weight type="chemical">16.00</Weight>
-<Weight type="physical">15.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Brosius, J.</Author>
-<Author>Chen, R.</Author>
-</Authors>
-<Citation>FEBS Lett. 68, 105-109, 1976</Citation>
-<Title>The primary structure of protein L16 located at the peptidyltransferase center of Escherichia coli ribosomes.</Title>
-<Xref>DOI:10.1016/0014-5793(76)80415-2</Xref>
-<Xref>PMID:786730</Xref>
-<Note>modified arginine observed in Escherichia coli ribosomal protein L16</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Arnold, R.J.</Author>
-<Author>Reilly, J.P.</Author>
-</Authors>
-<Citation>Anal. Biochem. 269, 105-112, 1999</Citation>
-<Title>Observation of Escherichia coli ribosomal proteins and their posttranslational modifications by mass spectrometry.</Title>
-<Xref>DOI:10.1006/abio.1998.3077</Xref>
-<Xref>PMID:10094780</Xref>
-<Note>top-down mass-spectrometry; in a private communication from J. Brosius the modification was identified as a probable hydroxyarginine</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ge, W.</Author>
-<Author>Wolf, A.</Author>
-<Author>Feng, T.</Author>
-<Author>Ho, C.H.</Author>
-<Author>Sekirnik, R.</Author>
-<Author>Zayer, A.</Author>
-<Author>Granatino, N.</Author>
-<Author>Cockman, M.E.</Author>
-<Author>Loenarz, C.</Author>
-<Author>Loik, N.D.</Author>
-<Author>Hardy, A.P.</Author>
-<Author>Claridge, T.D.</Author>
-<Author>Hamed, R.B.</Author>
-<Author>Chowdhury, R.</Author>
-<Author>Gong, L.</Author>
-<Author>Robinson, C.V.</Author>
-<Author>Trudgian, D.C.</Author>
-<Author>Jiang, M.</Author>
-<Author>Mackeen, M.M.</Author>
-<Author>McCullagh, J.S.</Author>
-<Author>Gordiyenko, Y.</Author>
-<Author>Thalhammer, A.</Author>
-<Author>Yamamoto, A.</Author>
-<Author>Yang, M.</Author>
-<Author>Liu-Yi, P.</Author>
-<Author>Zhang, Z.</Author>
-<Author>Schmidt-Zachmann, M.</Author>
-<Author>Kessler, B.M.</Author>
-<Author>Ratcliffe, P.J.</Author>
-<Author>Preston, G.M.</Author>
-<Author>Coleman, M.L.</Author>
-<Author>Schofield, C.J.</Author>
-</Authors>
-<Citation>Nature Chem. Biol. 8, 960-962, 2012</Citation>
-<Title>Oxygenase-catalyzed ribosome hydroxylation occurs in prokaryotes and humans.</Title>
-<Xref>DOI:10.1038/nchembio.1093</Xref>
-<Xref>PMID:23103944</Xref>
-<Note>mass spectrometry; NMR; radiolabeling; amino acid analysis indicate that the modification is the (2S,3R) diastereomer, by comparison with the synthetic diastereomers</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>van Staalduinen, L.M.</Author>
-<Author>Novakowski, S.K.</Author>
-<Author>Jia, Z.</Author>
-</Authors>
-<Citation>J. Mol. Biol. 426, 1898-1910, 2014</Citation>
-<Title>Structure and functional analysis of YcfD, a novel 2-oxoglutarate/Fe²⁺-dependent oxygenase involved in translational regulation in Escherichia coli.</Title>
-<Xref>DOI:10.1016/j.jmb.2014.02.008</Xref>
-<Xref>PMID:24530688</Xref>
-<Note>Jumonji C-domain-containing protein ycfD modifies E.coli ribosomal protein L16 arginine-81 to (3R)-3-hydroxy-L-arginine</Note>
-</ReferenceBlock>
-<Comment>The diastereomer (2S,3S)-3-hydroxyarginine is produced in non-ribosomal antibiotic peptides of Streptomyces vinaceus.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>ribosomal protein L16 arginine hydroxylase ycfD</EnzymeName>
-<EnzymeName>50S ribosomal protein L16 3-hydroxylase</EnzymeName>
-<EnzymeName>[50S ribosomal protein L16]-L-Arg81,2-oxoglutarate:oxygen oxidoreductase (3-hydroxylating) (EC 1.14.11.47)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>R</SequenceSpec>
-<Xref>PSI-MOD:01956</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__?3r?-3-hydroxyarginine__r">MOD_RES (3R)-3-hydroxyarginine</Feature>
-</Features>
-<Image src="/images/AA0601.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0601.PDB" />
-</Entry>
-<Entry id="AA0602">
-<Header>
-<Code>AA0602</Code>
-<Dates>
-<CreationDate>01-Mar-2013</CreationDate>
-<StrucRevDate>01-Mar-2013</StrucRevDate>
-<TextChngDate>30-Jun-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>2-hydroxyproline</Name>
-<AlternateName>2-oxidanylpyrrolidine-2-carboxylic acid</AlternateName>
-<AlternateName>alpha-hydroxyproline</AlternateName>
-<SystematicName>(2R)-2-hydroxypyrrolidine-2-carboxylic acid</SystematicName>
-<Xref>PDBHET:PXU</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 7 N 1 O 2</Formula>
-<Weight type="chemical">113.12</Weight>
-<Weight type="physical">113.047678</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0015">
-<Formula>C 0 H 0 N 0 O 1</Formula>
-<Weight type="chemical">16.00</Weight>
-<Weight type="physical">15.994915</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fadouloglou, V.E.</Author>
-<Author>Kapanidou, M.</Author>
-<Author>Agiomirgianaki, A.</Author>
-<Author>Arnaouteli, S.</Author>
-<Author>Bouriotis, V.</Author>
-<Author>Glykos, N.M.</Author>
-<Author>Kokkinidis, M.</Author>
-</Authors>
-<Citation>Acta Crystallogr. D Biol. Crystallogr. 69, 276-283, 2013</Citation>
-<Title>Structure determination through homology modelling and torsion-angle simulated annealing: application to a polysaccharide deacetylase from Bacillus cereus.</Title>
-<Xref>DOI:10.1107/S0907444912045829</Xref>
-<Xref>PMID:23385463</Xref>
-<Note>X-ray diffraction, 2.50 angstroms; electron density of a first row element appears to replace the alpha-carbon hydrogen in the neighborhood of a bound zinc atom; it is modeled as an alpha-hydroxyl group; there is no supporting chemical or mass-spectrometic evidence</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fadouloglou, V.E.</Author>
-<Author>Kokkinidis, M.</Author>
-<Author>Glykos, N.M.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, October 2012</Citation>
-<Description>Crystal structure of BC0361, a polysaccharide deacetylase from Bacillus cereus.</Description>
-<Xref>PDB:4HD5</Xref>
-<Note>X-ray diffraction, 2.50 angstroms</Note>
-</ReferenceBlock>
-<Comment>The chemical stability of this modification has been questioned. However, a similar modification in an homologous enzyme has apparently been observed by another group in work that has not yet been published.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>P</SequenceSpec>
-<Xref>PSI-MOD:01957</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>hydroxylation</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0602.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0602.PDB" />
-</Entry>
-<Entry id="AA0603">
-<Header>
-<Code>AA0603</Code>
-<Dates>
-<CreationDate>31-Mar-2013</CreationDate>
-<StrucRevDate>31-Mar-2013</StrucRevDate>
-<TextChngDate>31-Mar-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>bis-L-cysteinyl bisglutathion-S-yl diiron disulfide</Name>
-<AlternateName>mitochondrial glutaredoxin 2 dimer iron-sulfur cluster</AlternateName>
-<AlternateName>plant glutaredoxin C1 dimer iron-sulfur cluster</AlternateName>
-<SystematicName>di-mu-sulfido-bis(cysteinato)-1kappaS,2kappaS-bis(glutathionato)-1kappaS,2kappaS-diiron</SystematicName>
-<Xref>PDBHET:FES</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 26 Fe 2 H 40 N 8 O 14 S 6</Formula>
-<Weight type="chemical">992.70</Weight>
-<Weight type="physical">991.968699</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005">
-<Formula>C 20 Fe 2 H 30 N 6 O 12 S 4</Formula>
-<Weight type="chemical">786.42</Weight>
-<Weight type="physical">785.950329</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Johansson, C.</Author>
-<Author>Kavanagh, K.L.</Author>
-<Author>Gileadi, O.</Author>
-<Author>Oppermann, U.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 282, 3077-3082, 2007</Citation>
-<Title>Reversible sequestration of active site cysteines in a 2Fe-2S-bridged dimer provides a mechanism for glutaredoxin 2 regulation in human mitochondria.</Title>
-<Xref>DOI:10.1074/jbc.M608179200</Xref>
-<Xref>PMID:17121859</Xref>
-<Note>X-ray diffraction, 1.90 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Johansson, C.</Author>
-<Author>Smee, C.</Author>
-<Author>Kavanagh, K.L.</Author>
-<Author>Debreczeni, J.</Author>
-<Author>Von Delft, F.</Author>
-<Author>Gileadi, O.</Author>
-<Author>Arrowsmith, C.</Author>
-<Author>Weigelt, J.</Author>
-<Author>Edwards, A.</Author>
-<Author>Sundstrom, M.</Author>
-<Author>Oppermann, U.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, August 1996</Citation>
-<Description>The structure of dimeric human glutaredoxin 2.</Description>
-<Xref>PDB:2HT9</Xref>
-<Note>X-ray diffraction, 1.90 angstroms</Note>
-</ReferenceBlock>
-<Comment>The iron-sulfur cluster binding, dimeric form is described as "quiescent", and the reactivity is regulated by the relative redox potential determined by the GSH/GSSG ratio and the concentration of Fe(2+).</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C, C</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:01958</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>2Fe-2S</Keyword>
-<Keyword>iron-sulfur protein</Keyword>
-<Keyword>metalloprotein</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0603.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0603.PDB" />
-</Entry>
-<Entry id="AA0604">
-<Header>
-<Code>AA0604</Code>
-<Dates>
-<CreationDate>31-Mar-2013</CreationDate>
-<StrucRevDate>31-Mar-2013</StrucRevDate>
-<TextChngDate>31-Mar-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>tris-L-cysteinyl L-glutamato tetrairon tetrasulfide</Name>
-<SystematicName>tris-mu3-sulfido-tris(cysteinato)-1kappaS,2kappaS,3kappaS-glutamato-4kappaO(5),4kappaO(5')-tetrairon</SystematicName>
-<Xref>PDBHET:SF4</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 14 Fe 4 H 18 N 4 O 6 S 7</Formula>
-<Weight type="chemical">786.12</Weight>
-<Weight type="physical">785.666881</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005 AA0005 AA0006">
-<Formula>C 0 Fe 4 H -4 N 0 O 0 S 4</Formula>
-<Weight type="chemical">347.59</Weight>
-<Weight type="physical">347.596734</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Rekittke, I.</Author>
-<Author>Nonaka, T.</Author>
-<Author>Wiesner, J.</Author>
-<Author>Demmer, U.</Author>
-<Author>Warkentin, E.</Author>
-<Author>Jomaa, H.</Author>
-<Author>Ermler, U.</Author>
-</Authors>
-<Citation>FEBS Lett. 585, 447-451, 2011</Citation>
-<Title>Structure of the E-1-hydroxy-2-methyl-but-2-enyl-4-diphosphate synthase (GcpE) from Thermus thermophilus.</Title>
-<Xref>DOI:10.1016/j.febslet.2010.12.012</Xref>
-<Xref>PMID:21167158</Xref>
-<Note>X-ray diffraction, 2.50 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Rekittke, I.</Author>
-<Author>Nonaka, T.</Author>
-<Author>Wiesner, J.</Author>
-<Author>Demmer, U.</Author>
-<Author>Warkentin, E.</Author>
-<Author>Jomaa, H.</Author>
-<Author>Ermler, U.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, December 2010</Citation>
-<Description>Structure of GcpE (IspG) from Thermus thermophilus HB27.</Description>
-<Xref>PDB:2Y0F</Xref>
-<Note>X-ray diffraction, 2.50 angstroms</Note>
-</ReferenceBlock>
-<Comment>Both mono- and bidentate ligation by the glutamate were observed. Bidentate ligation is shown.</Comment>
-<Comment>The glutamate ligation is weak and is preferentially displaced by the substrate.</Comment>
-<SequenceCode>
-<SequenceSpec>C, C, C, E</SequenceSpec>
-<Condition>cross-link 4</Condition>
-<Xref>PSI-MOD:01959</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>4Fe-4S</Keyword>
-<Keyword>iron-sulfur protein</Keyword>
-<Keyword>metalloprotein</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0604.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0604.PDB" />
-</Entry>
-<Entry id="AA0605">
-<Header>
-<Code>AA0605</Code>
-<Dates>
-<CreationDate>31-Mar-2013</CreationDate>
-<StrucRevDate>31-Mar-2013</StrucRevDate>
-<TextChngDate>31-Dec-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>tris-L-cysteinyl L-glutamin-O6-yl tetrairon tetrasulfide</Name>
-<SystematicName>tris-mu3-sulfido-tris(cysteinato)-1kappaS,2kappaS,3kappaS-glutaminato-4kappaN(5)-tetrairon</SystematicName>
-<Xref>PDBHET:SF4</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 14 Fe 4 H 19 N 5 O 5 S 7</Formula>
-<Weight type="chemical">785.14</Weight>
-<Weight type="physical">784.682866</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0005 AA0005 AA0007">
-<Formula>C 0 Fe 4 H -4 N 0 O 0 S 4</Formula>
-<Weight type="chemical">347.59</Weight>
-<Weight type="physical">347.596734</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Dobritzsch, D.</Author>
-<Author>Ricagno, S.</Author>
-<Author>Schneider, G.</Author>
-<Author>Schnackerz, K.D.</Author>
-<Author>Lindqvist, Y.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 277, 13155-13166, 2002</Citation>
-<Title>Crystal structure of the productive ternary complex of dihydropyrimidine dehydrogenase with NADPH and 5-iodouracil. Implications for mechanism of inhibition and electron transfer.</Title>
-<Xref>DOI:10.1074/jbc.M111877200</Xref>
-<Xref>PMID:11796730</Xref>
-<Note>X-ray diffraction, 1.65 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Dobritzsch, D.</Author>
-<Author>Ricagno, S.</Author>
-<Author>Schneider, G.</Author>
-<Author>Schnackerz, K.D.</Author>
-<Author>Lindqvist, Y.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, January 2002</Citation>
-<Description>Dihydropyrimidine dehydrogenase (DPD) from pig, binaty complex with 5-iodouracil.</Description>
-<Xref>PDB:1GTE</Xref>
-<Note>X-ray diffraction, 1.65 angstroms</Note>
-</ReferenceBlock>
-<Comment>The glutamine ligation could be by either O(5) or N(5), and could not be distinguished at this resolution. The ligation was modeled as O(5) and that is the tautomeric form that is shown.</Comment>
-<SequenceCode>
-<SequenceSpec>C, C, C, Q</SequenceSpec>
-<Condition>cross-link 4</Condition>
-<Xref>PSI-MOD:01960</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>4Fe-4S</Keyword>
-<Keyword>iron-sulfur protein</Keyword>
-<Keyword>metalloprotein</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="metal__iron-sulfur (4fe-4s)__q">METAL Iron-sulfur (4Fe-4S)</Feature>
-</Features>
-<Image src="/images/AA0605.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0605.PDB" />
-</Entry>
-<Entry id="AA0606">
-<Header>
-<Code>AA0606</Code>
-<Dates>
-<CreationDate>31-May-2013</CreationDate>
-<StrucRevDate>31-May-2013</StrucRevDate>
-<TextChngDate>30-Jun-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N4-(2,4-diacetamido-2,4,6-trideoxy-D-glucosyl)-L-asparagine</Name>
-<AlternateName>DABA</AlternateName>
-<AlternateName>DATDH</AlternateName>
-<AlternateName>DiNAcBac</AlternateName>
-<AlternateName>N4-[2,4-bis(acetylamino)-2,4,6-trideoxy-beta-D-glucopyranosyl]-L-asparagine</AlternateName>
-<AlternateName>N4-[N,N-diacetylbacillosaminyl]asparagine</AlternateName>
-<AlternateName>N4-[N2,N4-diacetylbacillosaminyl]asparagine</AlternateName>
-<SystematicName>(2S)-2-amino-4-[(2,4-diacetylamino-2,4,6-trideoxy-beta-D-glucopyranosyl)amino]-4-oxobutanoic acid</SystematicName>
-<Xref>PDBHET:B6D</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 14 H 22 N 4 O 6</Formula>
-<Weight type="chemical">342.35</Weight>
-<Weight type="physical">342.153934</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0003">
-<Formula>C 10 H 16 N 2 O 4</Formula>
-<Weight type="chemical">228.25</Weight>
-<Weight type="physical">228.111007</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Young, N.M.</Author>
-<Author>Brisson, J.R.</Author>
-<Author>Kelly, J.</Author>
-<Author>Watson, D.C.</Author>
-<Author>Tessier, L.</Author>
-<Author>Lanthier, P.H.</Author>
-<Author>Jarrell, H.C.</Author>
-<Author>Cadotte, N.</Author>
-<Author>St. Michael, F.</Author>
-<Author>Aberg, E.</Author>
-<Author>Szymanski, C.M.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 277, 42530-42539, 2002</Citation>
-<Title>Structure of the N-linked glycan present on multiple glycoproteins in the Gram-negative bacterium, Campylobacter jejuni.</Title>
-<Xref>DOI:10.1074/jbc.M206114200</Xref>
-<Xref>PMID:12186869</Xref>
-<Note>mass spectrometric identification and (1)H-NMR characterization; large scale proteomic analysis; the spelling of St. Michael in the PubMed citation is corrected</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Min, T.</Author>
-<Author>Vedadi, M.</Author>
-<Author>Watson, D.C.</Author>
-<Author>Wasney, G.A.</Author>
-<Author>Munger, C.</Author>
-<Author>Cygler, M.</Author>
-<Author>Matte, A.</Author>
-<Author>Young, N.M.</Author>
-</Authors>
-<Citation>Biochemistry 48, 3057-3067, 2009</Citation>
-<Title>Specificity of Campylobacter jejuni adhesin PEB3 for phosphates and structural differences among its ligand complexes.</Title>
-<Xref>DOI:10.1021/bi802195d</Xref>
-<Xref>PMID:19236052</Xref>
-<Note>X-ray diffraction, 2.00 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Min, T.</Author>
-<Author>Matte, A.</Author>
-<Author>Cygler, M.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, December 2008</Citation>
-<Description>Crystal structure of glycosylated K135E PEB3.</Description>
-<Xref>PDB:3FIR</Xref>
-<Note>X-ray diffraction, 2.00 angstroms</Note>
-</ReferenceBlock>
-<Comment>Bacillosamine is a trivial name formed by modification of a non-standard monosaccharide parent name, and is not recommended by the IUPAC Nomenclature Committee. Some authors use bacillosamine to refer to the diacetylated form, rather than the unacetylated form.</Comment>
-<SequenceCode>
-<SequenceSpec>N</SequenceSpec>
-<Xref>PSI-MOD:01962</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0606.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0606.PDB" />
-</Entry>
-<Entry id="AA0607">
-<Header>
-<Code>AA0607</Code>
-<Dates>
-<CreationDate>31-May-2013</CreationDate>
-<StrucRevDate>31-May-2013</StrucRevDate>
-<TextChngDate>30-Jun-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-(2,4-diacetamido-2,4,6-trideoxy-D-glucosyl)-L-serine</Name>
-<AlternateName>DABA</AlternateName>
-<AlternateName>DATDH</AlternateName>
-<AlternateName>DiNAcBac</AlternateName>
-<AlternateName>O-[2,4-bis(acetylamino)-2,4,6-trideoxy-beta-D-glucopyranosyl]-L-serine</AlternateName>
-<AlternateName>O-[N,N-diacetylbacillosaminyl]serine</AlternateName>
-<AlternateName>O-[N2,N4-diacetylbacillosaminyl]serine</AlternateName>
-<SystematicName>(2S)-2-amino-4-[(2,4-diacetamido-2,4,6-trideoxy-beta-D-glucopyranosyl)oxy]propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 13 H 21 N 3 O 6</Formula>
-<Weight type="chemical">315.33</Weight>
-<Weight type="physical">315.143035</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 10 H 16 N 2 O 4</Formula>
-<Weight type="chemical">228.25</Weight>
-<Weight type="physical">228.111007</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Anonsen, J.H.</Author>
-<Author>Vik, Å.</Author>
-<Author>Egge-Jacobsen, W.</Author>
-<Author>Koomey, M.</Author>
-</Authors>
-<Citation>J. Proteome Res. 11, 5781-5793, 2012</Citation>
-<Title>An extended spectrum of target proteins and modification sites in the general O-linked protein glycosylation system in Neisseria gonorrhoeae.</Title>
-<Xref>DOI:10.1021/pr300584x</Xref>
-<Xref>PMID:23030644</Xref>
-<Note>mass spectrometric identification; large scale proteomic analysis</Note>
-</ReferenceBlock>
-<Comment>Bacillosamine is a trivial name formed by modification of a non-standard monosaccharide parent name, and is not recommended by the IUPAC Nomenclature Committee. Some authors use bacillosamine to refer to the diacetylated form, rather than the unacetylated form.</Comment>
-<Comment>For O-(2,4-diacetamido-2,4-dideoxy-D-glucosyl)-L-serine, see RESID:AA0499.</Comment>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>PSI-MOD:01963</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0607.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0607.PDB" />
-</Entry>
-<Entry id="AA0608">
-<Header>
-<Code>AA0608</Code>
-<Dates>
-<CreationDate>31-May-2013</CreationDate>
-<StrucRevDate>31-May-2013</StrucRevDate>
-<TextChngDate>30-Jun-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O-(2-acetamido-4-glyceramido-2,4,6-trideoxy-D-glucosyl)-L-serine</Name>
-<AlternateName>GATDH</AlternateName>
-<AlternateName>O-(2-acetamido-4-glyceramido-2,4,6-trideoxy-D-glucopyranosyl)-L-serine</AlternateName>
-<AlternateName>O-(N2-acetyl-N4-glycerylbacillosaminyl)-L-serine</AlternateName>
-<SystematicName>(2S)-2-amino-3-[(2-acetamido-4-glycerylamino-2,4,6-trideoxy-D-glucopyranosyl)oxy]propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 14 H 23 N 3 O 8</Formula>
-<Weight type="chemical">361.35</Weight>
-<Weight type="physical">361.148515</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 11 H 18 N 2 O 6</Formula>
-<Weight type="chemical">274.27</Weight>
-<Weight type="physical">274.116486</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Chamot-Rooke, J.</Author>
-<Author>Rousseau, B.</Author>
-<Author>Lanternier, F.</Author>
-<Author>Mikaty, G.</Author>
-<Author>Mairey, E.</Author>
-<Author>Malosse, C.</Author>
-<Author>Bouchoux, G.</Author>
-<Author>Pelicic, V.</Author>
-<Author>Camoin, L.</Author>
-<Author>Nassif, X.</Author>
-<Author>Duménil, G.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 104, 14783-14788, 2007</Citation>
-<Title>Alternative Neisseria spp. type IV pilin glycosylation with a glyceramido acetamido trideoxyhexose residue.</Title>
-<Xref>DOI:10.1073/pnas.0705335104</Xref>
-<Xref>PMID:17804791</Xref>
-<Note>mass spectrometric identification; the identity of the sugar is inferred by genomic analysis</Note>
-</ReferenceBlock>
-<Comment>The stereochemical identity of the sugar and the glyceryl group have not been established by chemical methods.</Comment>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>PSI-MOD:01964</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0608.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0608.PDB" />
-</Entry>
-<Entry id="AA0609">
-<Header>
-<Code>AA0609</Code>
-<Dates>
-<CreationDate>13-Sep-2013</CreationDate>
-<StrucRevDate>13-Sep-2013</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N(omega)-(N-acetylamino)glucosyl-L-arginine</Name>
-<AlternateName>N(omega)-(2-acetamido-2-deoxy-D-glucopyranosyl)-L-arginine</AlternateName>
-<AlternateName>N(omega)-(2-acetylamino-2-deoxy-D-glucopyranosyl)-L-arginine</AlternateName>
-<AlternateName>N(omega)-(2-N-acetylaminoglucosyl)arginine</AlternateName>
-<AlternateName>NG-(2-acetamido-2-deoxy-D-glucopyranosyl)-L-arginine</AlternateName>
-<AlternateName>NG-(2-acetylamino-2-deoxy-D-glucopyranosyl)-L-arginine</AlternateName>
-<AlternateName>NG-(2-N-acetylaminoglucosyl)arginine</AlternateName>
-<AlternateName>omega-N-(2-acetamido-2-deoxy-D-glucopyranosyl)-L-arginine</AlternateName>
-<AlternateName>omega-N-(2-acetylamino-2-deoxy-D-glucopyranosyl)-L-arginine</AlternateName>
-<AlternateName>omega-N-(2-N-acetylaminoglucosyl)arginine</AlternateName>
-<SystematicName>(2S)-2-amino-5-[(amino[(2-N-acetylamino-2-deoxy-D-glucopyranosyl)amino]methylidene)amino]pentanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 14 H 25 N 5 O 6</Formula>
-<Weight type="chemical">359.38</Weight>
-<Weight type="physical">359.180484</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0002">
-<Formula>C 8 H 13 N 1 O 5</Formula>
-<Weight type="chemical">203.19</Weight>
-<Weight type="physical">203.079373</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Li, S.</Author>
-<Author>Zhang, L.</Author>
-<Author>Yao, Q.</Author>
-<Author>Li, L.</Author>
-<Author>Dong, N.</Author>
-<Author>Rong, J.</Author>
-<Author>Gao, W.</Author>
-<Author>Ding, X.</Author>
-<Author>Sun, L.</Author>
-<Author>Chen, X.</Author>
-<Author>Chen, S.</Author>
-<Author>Shao, F.</Author>
-</Authors>
-<Citation>Nature 501, 242-246, 2013</Citation>
-<Title>Pathogen blocks host death receptor signalling by arginine GlcNAcylation of death domains.</Title>
-<Xref>DOI:10.1038/nature12436</Xref>
-<Xref>PMID:23955153</Xref>
-<Note>chromatographic and mass spectrometric identification; biosynthesis; the anomeric stereochemistry was not determined</Note>
-</ReferenceBlock>
-<Comment>This modification is produced in host proteins by a secretion system effector of some enteropathogenic bacteria. The anomeric form of the product has not been characterized; the beta form is presented.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>[protein]-L-arginine N-acetyl-D-glucosaminyl-transferase NleB (EC 2.4.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>R</SequenceSpec>
-<Xref>PSI-MOD:01967</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glycoprotein</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0609.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0609.PDB" />
-</Entry>
-<Entry id="AA0610">
-<Header>
-<Code>AA0610</Code>
-<Dates>
-<CreationDate>13-Sep-2013</CreationDate>
-<StrucRevDate>13-Sep-2013</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>(2R,3R,2'R)-3-methyllanthionine</Name>
-<AlternateName>(2R,3R,2'R)-2-amino-3-[(2-amino-2-carboxyethyl)thio]butanoic acid</AlternateName>
-<AlternateName>(2R,3R,6R)-2,6-diamino-3-methyl-4-thiaheptanedioic acid</AlternateName>
-<AlternateName>(2R,3R,6R)-3-methyllanthionine</AlternateName>
-<AlternateName>2-azanyl-3-[(2-azanyl-2-carboxyethyl)sulfanyl]butanoic acid</AlternateName>
-<AlternateName>3-methyl-L,L-lanthionine</AlternateName>
-<AlternateName>cysteine-3-L-butyrine thioether</AlternateName>
-<SystematicName>(2R,3R)-2-amino-3-([(2R)-2-amino-2-carboxyethyl]sulfanyl)butanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 10 N 2 O 2 S 1</Formula>
-<Weight type="chemical">186.23</Weight>
-<Weight type="physical">186.046299</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0017">
-<Formula>C 0 H -2 N 0 O -1 S 0</Formula>
-<Weight type="chemical">-18.02</Weight>
-<Weight type="physical">-18.010565</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Tang, W.</Author>
-<Author>van der Donk, W.A.</Author>
-</Authors>
-<Citation>Nature Chem. Biol. 9, 157-159, 2013</Citation>
-<Title>The sequence of the enterococcal cytolysin imparts unusual lanthionine stereochemistry.</Title>
-<Xref>DOI:10.1038/nchembio.1162</Xref>
-<Xref>PMID:23314913</Xref>
-<Note>chiral gas chromatographic and mass spectrometric identification</Note>
-</ReferenceBlock>
-<Comment>There are 3 chiral centers, so there are 8 possible stereoisomers. Bacterial peptidyl-cysteine dehydroalanine/dehydrobutyrine ligase and peptide conformation preferentially produce the (2S,3S,2'R) diastereomer. The cysteine maintains its L configuration (R chirality), while the threonine 2-aminobutanoate skeleton loses and then regains an L configuration (R chirality). For the (2S,3S,2'R), see RESID:AA0112.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>peptidyl-phosphoserine/phosphothreonine dehydratase (EC 4.2.1.-)</EnzymeName>
-<EnzymeName>peptidyl-cysteine dehydroalanine/dehydrobutyrine ligase (EC 6.2.-.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C, T</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:01968</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>lanthionine</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0610.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0610.PDB" />
-</Entry>
-<Entry id="AA0611">
-<Header>
-<Code>AA0611</Code>
-<Dates>
-<CreationDate>13-Sep-2013</CreationDate>
-<StrucRevDate>13-Sep-2013</StrucRevDate>
-<TextChngDate>13-Sep-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-(gamma-glutamyl-cysteinyl-glycyl)-cysteine</Name>
-<AlternateName>S-(glutathion-1-yl)-L-cysteine</AlternateName>
-<SystematicName>(2S)-2-amino-5-([(2R)-1-([2-([(2R)-2-amino-2-carboxyethyl]sulfanyl)-2-oxoethyl]amino)-1-oxo-3-sulfanylpropan-2-yl]amino)-5-oxopentanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 13 H 20 N 4 O 6 S 2</Formula>
-<Weight type="chemical">392.44</Weight>
-<Weight type="physical">392.082426</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 10 H 15 N 3 O 5 S 1</Formula>
-<Weight type="chemical">289.31</Weight>
-<Weight type="physical">289.073242</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Lin, C.H.</Author>
-<Author>Kwon, D.S.</Author>
-<Author>Bollinger Jr., J.M.</Author>
-<Author>Walsh, C.T.</Author>
-</Authors>
-<Citation>Biochemistry 36, 14930-14938, 1997</Citation>
-<Title>Evidence for a glutathionyl-enzyme intermediate in the amidase activity of the bifunctional glutathionylspermidine synthetase/amidase from Escherichia coli.</Title>
-<Xref>DOI:10.1021/bi9714464</Xref>
-<Xref>PMID:9398217</Xref>
-<Note>chemical characterization; directed mutation analysis</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>PSI-MOD:01969</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>glutathione</Keyword>
-<Keyword>thioester bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="act_site__s-(gamma-glutamyl-cysteinyl-glycyl)-cysteine intermediate__c">ACT_SITE S-(gamma-glutamyl-cysteinyl-glycyl)-cysteine intermediate</Feature>
-</Features>
-<Image src="/images/AA0611.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0611.PDB" />
-</Entry>
-<Entry id="AA0612">
-<Header>
-<Code>AA0612</Code>
-<Dates>
-<CreationDate>13-Sep-2013</CreationDate>
-<StrucRevDate>13-Sep-2013</StrucRevDate>
-<TextChngDate>30-Sep-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>5-glutamyl glutamic acid</Name>
-<AlternateName>(2S)-2-[(4S)-4-amino-4-carboxybutanamido]pentanedioic acid</AlternateName>
-<AlternateName>2-([4-azanyl-4-carboxybutanoyl]azanyl)pentanedioic acid</AlternateName>
-<AlternateName>gamma-glutamylglutamate</AlternateName>
-<AlternateName>isoglutamyl glutamic acid</AlternateName>
-<AlternateName>isoglutamyl monoglutamic acid</AlternateName>
-<AlternateName>N-(gamma-L-glutamyl)-L-glutamic acid</AlternateName>
-<SystematicName>(2S)-2-([(4S)-4-amino-4-carboxybutanoyl]amino)pentanedioic acid</SystematicName>
-<Xref>CAS:1116-22-9</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 10 H 14 N 2 O 6</Formula>
-<Weight type="chemical">258.23</Weight>
-<Weight type="physical">258.085186</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0006">
-<Formula>C 5 H 7 N 1 O 3</Formula>
-<Weight type="chemical">129.12</Weight>
-<Weight type="physical">129.042593</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ouchi, T.</Author>
-<Author>Tomita, T.</Author>
-<Author>Horie, A.</Author>
-<Author>Yoshida, A.</Author>
-<Author>Takahashi, K.</Author>
-<Author>Nishida, H.</Author>
-<Author>Lassak, K.</Author>
-<Author>Taka, H.</Author>
-<Author>Mineki, R.</Author>
-<Author>Fujimura, T.</Author>
-<Author>Kosono, S.</Author>
-<Author>Nishiyama, C.</Author>
-<Author>Masui, R.</Author>
-<Author>Kuramitsu, S.</Author>
-<Author>Albers, S.V.</Author>
-<Author>Kuzuyama, T.</Author>
-<Author>Nishiyama, M.</Author>
-</Authors>
-<Citation>Nature Chem. Biol. 9, 277-283, 2013</Citation>
-<Title>Lysine and arginine biosyntheses mediated by a common carrier protein in Sulfolobus.</Title>
-<Xref>DOI:10.1038/nchembio.1200</Xref>
-<Xref>PMID:23434852</Xref>
-<Note>biosynthesis; mass spectrometric detection</Note>
-</ReferenceBlock>
-<Comment>This entry is for isoglutamyl glutamic acid where there is a single glutamic acid attached to a peptide glutamyl residue by an isopeptide bond. For L-isoglutamyl-polyglutamic acid where there are 2 to 6 alpha-peptide linked glutamic acid residues attached to a peptide glutamyl residue by an isopeptide bond, see RESID:AA0202.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>glutamate--LysW ligase, ArgX (EC 6.3.2.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>E</SequenceSpec>
-<Xref>PSI-MOD:01970</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>isopeptide bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__5-glutamyl glutamate__e">MOD_RES 5-glutamyl glutamate</Feature>
-</Features>
-<Image src="/images/AA0612.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0612.PDB" />
-</Entry>
-<Entry id="AA0613">
-<Header>
-<Code>AA0613</Code>
-<Dates>
-<CreationDate>13-Sep-2013</CreationDate>
-<StrucRevDate>13-Sep-2013</StrucRevDate>
-<TextChngDate>13-Sep-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>5-glutamyl N2-ornithine</Name>
-<AlternateName>(2S)-5-amino-2-([(4S)-4-amino-4-carboxybutanoyl]amino)pentanoic acid</AlternateName>
-<AlternateName>4-amino-5-[(4-amino-1-carboxy-butyl)amino]-5-ketovaleric acid</AlternateName>
-<AlternateName>4-amino-5-[(4-amino-1-carboxy-butyl)amino]-5-oxopentanoic acid</AlternateName>
-<AlternateName>gamma-glutamylornithine</AlternateName>
-<AlternateName>N2-(gamma-glutamyl)ornithine</AlternateName>
-<AlternateName>N2-(L-isoglutamyl)-L-ornithine</AlternateName>
-<SystematicName>(2S)-5-amino-2-[(4S)-4-amino-4-carboxybutanamido]pentanoic acid</SystematicName>
-<Xref>CAS:56523-61-6</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 10 H 17 N 3 O 4</Formula>
-<Weight type="chemical">243.26</Weight>
-<Weight type="physical">243.121906</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0006">
-<Formula>C 5 H 10 N 2 O 1</Formula>
-<Weight type="chemical">114.15</Weight>
-<Weight type="physical">114.079313</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Ouchi, T.</Author>
-<Author>Tomita, T.</Author>
-<Author>Horie, A.</Author>
-<Author>Yoshida, A.</Author>
-<Author>Takahashi, K.</Author>
-<Author>Nishida, H.</Author>
-<Author>Lassak, K.</Author>
-<Author>Taka, H.</Author>
-<Author>Mineki, R.</Author>
-<Author>Fujimura, T.</Author>
-<Author>Kosono, S.</Author>
-<Author>Nishiyama, C.</Author>
-<Author>Masui, R.</Author>
-<Author>Kuramitsu, S.</Author>
-<Author>Albers, S.V.</Author>
-<Author>Kuzuyama, T.</Author>
-<Author>Nishiyama, M.</Author>
-</Authors>
-<Citation>Nature Chem. Biol. 9, 277-283, 2013</Citation>
-<Title>Lysine and arginine biosyntheses mediated by a common carrier protein in Sulfolobus.</Title>
-<Xref>DOI:10.1038/nchembio.1200</Xref>
-<Xref>PMID:23434852</Xref>
-<Note>biosynthesis; this intermediate product was not directly observed but was inferred</Note>
-</ReferenceBlock>
-<Comment>This modification is probably produced on the C-terminal glutamic acid of a carrier protein as one of a series of intermediates.</Comment>
-<SequenceCode>
-<SequenceSpec>E</SequenceSpec>
-<Xref>PSI-MOD:01971</Xref>
-</SequenceCode>
-<Source>hypothetical</Source>
-<Keywords>
-<Keyword>isopeptide bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__5-glutamyl n2-ornithine__e">MOD_RES 5-glutamyl N2-ornithine</Feature>
-</Features>
-<Image src="/images/AA0613.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0613.PDB" />
-</Entry>
-<Entry id="AA0614">
-<Header>
-<Code>AA0614</Code>
-<Dates>
-<CreationDate>13-Sep-2013</CreationDate>
-<StrucRevDate>13-Sep-2013</StrucRevDate>
-<TextChngDate>30-Sep-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>5-glutamyl coenzyme A thioester</Name>
-<AlternateName>(2S)-2-amino-5-(2-[([3-([(2R)-2-hydroxy-3,3-dimethyl-4-([3'-phospho-adenosyl-5'-diphosphoryl]-oxy)-butanoyl]-amino)-propanoyl]-amino)-ethyl]-sulfanyl)-5-oxopentanoic acid</AlternateName>
-<AlternateName>5-glutamyl 4-[(3'-phospho-adenosyl-5'-diphosphoryl)oxy]pantetheine thioester</AlternateName>
-<SystematicName>(2S)-2-amino-5-([2-(3-[(2R)-2-hydroxy-3,3-dimethyl-4-([3'-phospho-adenosyl-5'-diphosphoryl]-oxy)-butanamido]-propanamido)-ethyl]-sulfanyl)-5-oxopentanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 26 H 41 N 8 O 18 P 3 S 1</Formula>
-<Weight type="chemical">878.63</Weight>
-<Weight type="physical">878.147237</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0006">
-<Formula>C 21 H 34 N 7 O 15 P 3 S 1</Formula>
-<Weight type="chemical">749.52</Weight>
-<Weight type="physical">749.104644</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Rochet, J.C.</Author>
-<Author>Bridger, W.A.</Author>
-</Authors>
-<Citation>Protein Sci. 3, 975-981, 1994</Citation>
-<Title>Identification of glutamate 344 as the catalytic residue in the active site of pig heart CoA transferase.</Title>
-<Xref>DOI:10.1002/pro.5560030613</Xref>
-<Xref>PMID:7915164</Xref>
-<Note>mass spectrometric identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fraser, M.E.</Author>
-<Author>Hayakawa, K.</Author>
-<Author>Brown, W.D.</Author>
-</Authors>
-<Citation>Biochemistry 49, 10319-10328, 2010</Citation>
-<Title>Catalytic role of the conformational change in succinyl-CoA:3-oxoacid CoA transferase on binding CoA.</Title>
-<Xref>DOI:10.1021/bi100659s</Xref>
-<Xref>PMID:20977214</Xref>
-<Note>X-ray diffraction, 2.30 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Fraser, M.E.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, September 2010</Citation>
-<Description>Succinyl-CoA:3-ketoacid CoA transferase from pig heart covalently bound to CoA.</Description>
-<Xref>PDB:3OXO</Xref>
-<Note>X-ray diffraction, 2.30 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Rangarajan, E.S.</Author>
-<Author>Li, Y.</Author>
-<Author>Ajamian, E.</Author>
-<Author>Iannuzzi, P.</Author>
-<Author>Kernaghan, S.D.</Author>
-<Author>Fraser, M.E.</Author>
-<Author>Cygler, M.</Author>
-<Author>Matte, A.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 280, 42919-42928, 2005</Citation>
-<Title>Crystallographic trapping of the glutamyl-CoA thioester intermediate of family I CoA transferases.</Title>
-<Xref>DOI:10.1074/jbc.M510522200</Xref>
-<Xref>PMID:16253988</Xref>
-<Note>X-ray diffraction, 2.00 angstroms</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Rangarajan, E.S.</Author>
-<Author>Li, Y.</Author>
-<Author>Ajamian, E.</Author>
-<Author>Iannuzzi, P.</Author>
-<Author>Kernaghan, S.D.</Author>
-<Author>Fraser, M.E.</Author>
-<Author>Cygler, M.</Author>
-<Author>Matte, A.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, July 2005</Citation>
-<Description>Crystal structure of acyl-CoA transferase from E. coli O157:H7 (YdiF)- thioester complex with CoA- 1.</Description>
-<Xref>PDB:2AHV</Xref>
-<Note>X-ray diffraction, 2.00 angstroms</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>E</SequenceSpec>
-<Xref>PSI-MOD:01972</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>coenzyme A</Keyword>
-<Keyword>thioester bond</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="act_site__5-glutamyl coenzyme a thioester intermediate__e">5-glutamyl coenzyme A thioester intermediate</Feature>
-</Features>
-<Image src="/images/AA0614.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0614.PDB" />
-</Entry>
-<Entry id="AA0615">
-<Header>
-<Code>AA0615</Code>
-<Dates>
-<CreationDate>13-Sep-2013</CreationDate>
-<StrucRevDate>13-Sep-2013</StrucRevDate>
-<TextChngDate>13-Sep-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N6-(3-phosphoglyceryl)-L-lysine</Name>
-<AlternateName>(2S)-2-amino-6-([(2R)-2-hydroxy-3-(phosphonooxy)propanoyl]amino)hexanoic acid</AlternateName>
-<AlternateName>3-phosphoglyceryl-lysine</AlternateName>
-<SystematicName>(2S)-2-amino-6-[(2R)-2-hydroxy-3-(phosphonooxy)propanamido]hexanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 9 H 17 N 2 O 7 P 1</Formula>
-<Weight type="chemical">296.22</Weight>
-<Weight type="physical">296.077338</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0012">
-<Formula>C 3 H 5 N 0 O 6 P 1</Formula>
-<Weight type="chemical">168.04</Weight>
-<Weight type="physical">167.982375</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Moellering, R.E.</Author>
-<Author>Cravatt, B.F.</Author>
-</Authors>
-<Citation>Science 341, 549-553, 2013</Citation>
-<Title>Functional lysine modification by an intrinsically reactive primary glycolytic metabolite.</Title>
-<Xref>DOI:10.1126/science.1238327</Xref>
-<Xref>PMID:23908237</Xref>
-<Note>mass-spectrometic detection; radiolabeling</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>K</SequenceSpec>
-<Xref>PSI-MOD:01973</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>phosphoprotein</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0615.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0615.PDB" />
-</Entry>
-<Entry id="AA0616">
-<Header>
-<Code>AA0616</Code>
-<Dates>
-<CreationDate>13-Sep-2013</CreationDate>
-<StrucRevDate>13-Sep-2013</StrucRevDate>
-<TextChngDate>13-Sep-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-methyl-L-methionine</Name>
-<AlternateName>(2S)-2-amino-4-(dimethylsulfonio)butanoate</AlternateName>
-<AlternateName>S-methylmethionine</AlternateName>
-<AlternateName>S-methylmethioninium</AlternateName>
-<AlternateName>vitamin U</AlternateName>
-<AlternateName>[(3S)-3-amino-3-carboxypropyl](dimethyl)sulfonium</AlternateName>
-<SystematicName>(3S)-(3-amino-3-carboxypropyl)dimethylsulfanium</SystematicName>
-<Xref>CAS:4727-40-6</Xref>
-<Xref>ChEBI:17728</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 12 N 1 O 1 S 1</Formula>
-<FormalCharge>1+</FormalCharge>
-<Weight type="chemical">146.23</Weight>
-<Weight type="physical">146.063411</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0013">
-<Formula>C 1 H 3 N 0 O 0 S 0</Formula>
-<FormalCharge>1+</FormalCharge>
-<Weight type="chemical">15.03</Weight>
-<Weight type="physical">15.022927</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Patananan, A.N.</Author>
-<Author>Palmer, J.M.</Author>
-<Author>Garvey, G.S.</Author>
-<Author>Keller, N.P.</Author>
-<Author>Clarke, S.G.</Author>
-</Authors>
-<Citation>J. Biol. Chem. 288, 14032-14045, 2013</Citation>
-<Title>A novel automethylation reaction in the Aspergillus nidulans LaeA protein generates S-methylmethionine.</Title>
-<Xref>DOI:10.1074/jbc.M113.465765</Xref>
-<Xref>PMID:23532849</Xref>
-<Note>radiolabeling detection; chromatographic identification; no protein was detected as a methylation target other than the LaeA protein itself, but the modified methionine was not required for transcription regulating activity</Note>
-</ReferenceBlock>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>M</SequenceSpec>
-<Xref>PSI-MOD:01974</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>methylated amino acid</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0616.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0616.PDB" />
-</Entry>
-<Entry id="AA0617">
-<Header>
-<Code>AA0617</Code>
-<Dates>
-<CreationDate>30-Sep-2013</CreationDate>
-<StrucRevDate>30-Sep-2013</StrucRevDate>
-<TextChngDate>31-Dec-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>S-poly(3-hydroxybutyrate)-L-cysteine</Name>
-<AlternateName>S-poly(3-hydroxybutanoate)cysteine</AlternateName>
-<AlternateName>S-poly(3-hydroxybutanoic acid)cysteine</AlternateName>
-<AlternateName>S-poly(3-hydroxybutyrate)cysteine</AlternateName>
-<AlternateName>S-poly(3-hydroxybutyric acid)cysteine</AlternateName>
-<AlternateName>S-poly(beta-hydroxybutyrate)cysteine</AlternateName>
-<AlternateName>S-poly[(R)-3-hydroxybutyrate]cysteine</AlternateName>
-<SystematicName>(alpha)-([(2R)-2-amino-2-carboxyethyl]sulfanyl)-(omega)-[(3R)-3-hydroxybutanoyl]-poly([(3R)-3-methyl-1-oxopropane-1,3-diyl]oxy)</SystematicName>
-<Xref>CAS:29435-48-1</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 11 H 17 N 1 O 5 S 1</Formula>
-<Weight type="chemical">275.32</Weight>
-<Weight type="physical">275.082744</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005">
-<Formula>C 8 H 12 N 0 O 4 S 0</Formula>
-<Weight type="chemical">172.18</Weight>
-<Weight type="physical">172.073559</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Müh, U.</Author>
-<Author>Sinskey, A.J.</Author>
-<Author>Kirby, D.P.</Author>
-<Author>Lane, W.S.</Author>
-<Author>Stubbe, J.</Author>
-</Authors>
-<Citation>Biochemistry 38, 826-837, 1999</Citation>
-<Title>PHA synthase from chromatium vinosum: cysteine 149 is involved in covalent catalysis.</Title>
-<Xref>DOI:10.1021/bi9818319</Xref>
-<Xref>PMID:9888824</Xref>
-<Note>biosynthesis; chromatographic and mass spectrometric identification; radiolabeling; directed mutation analysis; the production of poly-3-hydroxybutyrate by Escherichia coli polyhydroxybutyrate synthase requires Cys-149</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Li, P.</Author>
-<Author>Chakraborty, S.</Author>
-<Author>Stubbe, J.</Author>
-</Authors>
-<Citation>Biochemistry 48, 9202-9211, 2009</Citation>
-<Title>Detection of covalent and noncovalent intermediates in the polymerization reaction catalyzed by a C149S class III polyhydroxybutyrate synthase.</Title>
-<Xref>DOI:10.1021/bi901329b</Xref>
-<Xref>PMID:19711985</Xref>
-<Note>biosynthesis; chromatographic and mass spectrometric identification; radiolabeling; directed mutation analysis; the autocatalytic covalent modification by polymeric 3-hydroxybutyrate of Cys-149 in Escherichia coli polyhydroxybutyrate synthase is demonstrated</Note>
-</ReferenceBlock>
-<Comment>The mechanism of biosynthesis may involve transfer of the polymer to and from a noncovalently bound coenzyme A.</Comment>
-<Comment>The intermediate modification with two polymeric units is presented.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>autocatalytic</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>C</SequenceSpec>
-<Xref>PSI-MOD:01975</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0617.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0617.PDB" />
-</Entry>
-<Entry id="AA0618">
-<Header>
-<Code>AA0618</Code>
-<Dates>
-<CreationDate>30-Sep-2013</CreationDate>
-<StrucRevDate>30-Sep-2013</StrucRevDate>
-<TextChngDate>30-Sep-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>O3-(poly-3-hydroxybutyrate)-L-serine</Name>
-<AlternateName>O3-poly(3-hydroxybutanoate)serine</AlternateName>
-<AlternateName>O3-poly(3-hydroxybutanoic acid)serine</AlternateName>
-<AlternateName>O3-poly(3-hydroxybutyrate)serine</AlternateName>
-<AlternateName>O3-poly(3-hydroxybutyric acid)serine</AlternateName>
-<AlternateName>O3-poly(beta-hydroxybutyrate)serine</AlternateName>
-<AlternateName>O3-poly[(R)-3-hydroxybutyrate]serine</AlternateName>
-<SystematicName>(2S)-2-amino-3-[([(3R)-3-hydroxybutanoyl]oxy)-poly([(3R)-3-methyl-1-oxopropane-1,3-diyl]oxy)]propanoic acid</SystematicName>
-<Xref>CAS:29435-48-1</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 11 H 17 N 1 O 6</Formula>
-<Weight type="chemical">259.26</Weight>
-<Weight type="physical">259.105587</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0016">
-<Formula>C 8 H 12 N 0 O 4</Formula>
-<Weight type="chemical">172.18</Weight>
-<Weight type="physical">172.073559</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Xian, M.</Author>
-<Author>Fuerst, M.M.</Author>
-<Author>Shabalin, Y.</Author>
-<Author>Reusch, R.N.</Author>
-</Authors>
-<Citation>Biochim. Biophys. Acta 1768, 2660-2666, 2007</Citation>
-<Title>Sorting signal of Escherichia coli OmpA is modified by oligo-(R)-3-hydroxybutyrate.</Title>
-<Xref>DOI:10.1016/j.bbamem.2007.06.019</Xref>
-<Xref>PMID:17659252</Xref>
-<Note>chromatographic and mass spectrometric identification; directed mutation analysis; probably both Ser-184 and Ser-188 of E.coli OmpA (UniProt:P0A910) are modified by a polymer of 6-10 units, but degradation during isolation was possible</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Negoda, A.</Author>
-<Author>Negoda, E.</Author>
-<Author>Reusch, R.N.</Author>
-</Authors>
-<Citation>Biochim. Biophys. Acta 1798, 1480-1484, 2010</Citation>
-<Title>Oligo-(R)-3-hydroxybutyrate modification of sorting signal enables pore formation by Escherichia coli OmpA.</Title>
-<Xref>DOI:10.1016/j.bbamem.2009.11.023</Xref>
-<Xref>PMID:20004640</Xref>
-<Note>modification of OmpA is necessary for targeting to membrane and pore formation</Note>
-</ReferenceBlock>
-<Comment>The mechanism for transfer of the polymer from the synthase is uncertain.</Comment>
-<Comment>The modification with two polymeric units is presented.</Comment>
-<SequenceCode>
-<SequenceSpec>S</SequenceSpec>
-<Xref>PSI-MOD:01976</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0618.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0618.PDB" />
-</Entry>
-<Entry id="AA0619">
-<Header>
-<Code>AA0619</Code>
-<Dates>
-<CreationDate>31-Dec-2013</CreationDate>
-<StrucRevDate>31-Dec-2013</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N,N,N-trimethylglycine</Name>
-<AlternateName>(trimethylammonio)ethanoic acid</AlternateName>
-<AlternateName>1-carboxy-N,N,N-trimethylmethanazanium</AlternateName>
-<AlternateName>2-trimethylammonioacetate</AlternateName>
-<AlternateName>betaine</AlternateName>
-<AlternateName>carboxymethyl-trimethylazanium</AlternateName>
-<AlternateName>glycine betaine</AlternateName>
-<AlternateName>N,N,N-trimethylglycine cation</AlternateName>
-<AlternateName>N,N,N-trimethylglycinium</AlternateName>
-<SystematicName>carboxy-N,N,N-trimethylmethanaminium</SystematicName>
-<Xref>CAS:107-43-7</Xref>
-<Xref>ChEBI:17750</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 5 H 11 N 1 O 1</Formula>
-<FormalCharge>1+</FormalCharge>
-<Weight type="chemical">101.15</Weight>
-<Weight type="physical">101.083515</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0008">
-<Formula>C 3 H 7 N 0 O 0</Formula>
-<FormalCharge>1+</FormalCharge>
-<Weight type="chemical">43.09</Weight>
-<Weight type="physical">43.054227</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bailey, A.O.</Author>
-<Author>Panchenko, T.</Author>
-<Author>Sathyan, K.M.</Author>
-<Author>Petkowski, J.J.</Author>
-<Author>Pai, P.J.</Author>
-<Author>Bai, D.L.</Author>
-<Author>Russell, D.H.</Author>
-<Author>Macara, I.G.</Author>
-<Author>Shabanowitz, J.</Author>
-<Author>Hunt, D.F.</Author>
-<Author>Black, B.E.</Author>
-<Author>Foltz, D.R.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 110, 11827-11832, 2013</Citation>
-<Title>Posttranslational modification of CENP-A influences the conformation of centromeric chromatin.</Title>
-<Xref>DOI:10.1073/pnas.1300325110</Xref>
-<Xref>PMID:23818633</Xref>
-<Note>mass spectrometric identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Dai, X.</Author>
-<Author>Otake, K.</Author>
-<Author>You, C.</Author>
-<Author>Cai, Q.</Author>
-<Author>Wang, Z.</Author>
-<Author>Masumoto, H.</Author>
-<Author>Wang, Y.</Author>
-</Authors>
-<Citation>J. Proteome Res. 12, 4167-4175, 2013</Citation>
-<Title>Identification of novel α-n-methylation of CENP-B that regulates its binding to the centromeric DNA.</Title>
-<Xref>DOI:10.1021/pr400498y</Xref>
-<Xref>PMID:23978223</Xref>
-<Note>mass spectrometric identification</Note>
-</ReferenceBlock>
-<Comment>This modification is the major post-translational modification in the methylation of N-terminal glycine. See also RESID:AA0063 and RESID:AA0620.</Comment>
-<Comment>Consult FAQ at http://pir.georgetown.edu/resid/faq.shtml#q12 concerning calculation of the difference formula.</Comment>
-<Comment>It is not clear whether the N-terminal methyltransferase responsible for methylating N-terminal glycine is distinguishable from the enzyme activities of EC 2.1.1.244 or EC 2.1.1.299.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>protein N-terminal methyltransferase (EC 2.1.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>G</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>PSI-MOD:01982</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-<Keyword>methylated amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n,n,n-trimethylglycine__g">MOD_RES N,N,N-trimethylglycine</Feature>
-</Features>
-<Image src="/images/AA0619.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0619.PDB" />
-</Entry>
-<Entry id="AA0620">
-<Header>
-<Code>AA0620</Code>
-<Dates>
-<CreationDate>31-Dec-2013</CreationDate>
-<StrucRevDate>31-Dec-2013</StrucRevDate>
-<TextChngDate>31-May-2018</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>N,N-dimethylglycine</Name>
-<AlternateName>1-carboxy-N,N-dimethylaminomethane</AlternateName>
-<AlternateName>2-(dimethylamino)acetic acid</AlternateName>
-<AlternateName>vitamin B16</AlternateName>
-<SystematicName>(dimethylamino)ethanoic acid</SystematicName>
-<Xref>CAS:1118-68-9</Xref>
-<Xref>ChEBI:17724</Xref>
-<Xref>PDBHET:DMG</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 4 H 8 N 1 O 1</Formula>
-<Weight type="chemical">86.11</Weight>
-<Weight type="physical">86.060589</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0008">
-<Formula>C 2 H 4 N 0 O 0</Formula>
-<Weight type="chemical">28.05</Weight>
-<Weight type="physical">28.031300</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Bailey, A.O.</Author>
-<Author>Panchenko, T.</Author>
-<Author>Sathyan, K.M.</Author>
-<Author>Petkowski, J.J.</Author>
-<Author>Pai, P.J.</Author>
-<Author>Bai, D.L.</Author>
-<Author>Russell, D.H.</Author>
-<Author>Macara, I.G.</Author>
-<Author>Shabanowitz, J.</Author>
-<Author>Hunt, D.F.</Author>
-<Author>Black, B.E.</Author>
-<Author>Foltz, D.R.</Author>
-</Authors>
-<Citation>Proc. Natl. Acad. Sci. U.S.A. 110, 11827-11832, 2013</Citation>
-<Title>Posttranslational modification of CENP-A influences the conformation of centromeric chromatin.</Title>
-<Xref>DOI:10.1073/pnas.1300325110</Xref>
-<Xref>PMID:23818633</Xref>
-<Note>mass spectrometric identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Dai, X.</Author>
-<Author>Otake, K.</Author>
-<Author>You, C.</Author>
-<Author>Cai, Q.</Author>
-<Author>Wang, Z.</Author>
-<Author>Masumoto, H.</Author>
-<Author>Wang, Y.</Author>
-</Authors>
-<Citation>J. Proteome Res. 12, 4167-4175, 2013</Citation>
-<Title>Identification of novel α-n-methylation of CENP-B that regulates its binding to the centromeric DNA.</Title>
-<Xref>DOI:10.1021/pr400498y</Xref>
-<Xref>PMID:23978223</Xref>
-<Note>mass spectrometric identification</Note>
-</ReferenceBlock>
-<Comment>This modification is a minor post-translational modification in the incomplete trimethylation of N-terminal glycine. See also RESID:AA0063 and RESID:AA0619.</Comment>
-<Comment>This modification is readily formed artifactually from N-terminal glycine by reductive methylation using formaldehyde.</Comment>
-<Comment>It is not clear whether the N-terminal methyltransferase responsible for methylating N-terminal glycine is distinguishable from the enzyme activities of EC 2.1.1.244 or EC 2.1.1.299.</Comment>
-<GeneratingEnzyme>
-<EnzymeName>protein N-terminal methyltransferase (EC 2.1.1.-)</EnzymeName>
-</GeneratingEnzyme>
-<SequenceCode>
-<SequenceSpec>G</SequenceSpec>
-<Condition>amino-terminal</Condition>
-<Xref>PSI-MOD:01983</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>blocked amino end</Keyword>
-<Keyword>methylated amino end</Keyword>
-</Keywords>
-<Features>
-<Feature type="UniProt" key="mod_res__n,n-dimethylglycine__g">MOD_RES N,N-dimethylglycine</Feature>
-</Features>
-<Image src="/images/AA0620.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0620.PDB" />
-</Entry>
-<Entry id="AA0621">
-<Header>
-<Code>AA0621</Code>
-<Dates>
-<CreationDate>31-Dec-2013</CreationDate>
-<StrucRevDate>31-Dec-2013</StrucRevDate>
-<TextChngDate>31-Dec-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>2-(L-cystein-S-yl)-L-alanine</Name>
-<AlternateName>(2R,5R)-2,5-diamino-5-methyl-4-thiahexanedioic acid</AlternateName>
-<AlternateName>alpha-(L-cystein-S-yl)-L-alanine</AlternateName>
-<SystematicName>(2R)-2-amino-2-[(2R)-2-amino-2-carboxyethyl]sulfanyl-3-hydroxybutanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 8 N 2 O 2 S 1</Formula>
-<Weight type="chemical">172.20</Weight>
-<Weight type="physical">172.030649</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0001 AA0005">
-<Formula>C 0 H -2 N 0 O 0 S 0</Formula>
-<Weight type="chemical">-2.02</Weight>
-<Weight type="physical">-2.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sit, C.S.</Author>
-<Author>McKay, R.T.</Author>
-<Author>Hill, C.</Author>
-<Author>Ross, R.P.</Author>
-<Author>Vederas, J.C.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 133, 7680-7683, 2011</Citation>
-<Title>The 3D structure of thuricin CD, a two-component bacteriocin with cysteine sulfur to α-carbon cross-links.</Title>
-<Xref>DOI:10.1021/ja201802f</Xref>
-<Xref>PMID:21526839</Xref>
-<Note>(1)H-NMR, (13)C-NMR and (15)N-NMR geometry constraint modeling; stereochemical determination</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sit, C.S.</Author>
-<Author>McKay, R.T.</Author>
-<Author>Hill, C.</Author>
-<Author>Ross, R.P.</Author>
-<Author>Vederas, J.C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, February 2011</Citation>
-<Description>Trn- peptide of the two-component bacteriocin thuricin CD.</Description>
-<Xref>PDB:2LA0</Xref>
-<Note>this is Trn-beta peptide; (1)H-NMR, (13)C-NMR and (15)N-NMR geometry constraint modeling; stereochemical determination</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>A, C</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:01984</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0621.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0621.PDB" />
-</Entry>
-<Entry id="AA0622">
-<Header>
-<Code>AA0622</Code>
-<Dates>
-<CreationDate>31-Dec-2013</CreationDate>
-<StrucRevDate>31-Dec-2013</StrucRevDate>
-<TextChngDate>31-Dec-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>2-(L-cystein-S-yl)-D-asparagine</Name>
-<AlternateName>alpha-(L-cystein-S-yl)-D-asparagine</AlternateName>
-<SystematicName>(2S)-2,4-diamino-2-([(2R)-2-amino-2-carboxyethyl]sulfanyl)-4-oxobutanoic acid</SystematicName>
-<Xref>PDBHET:DSG</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 9 N 3 O 3 S 1</Formula>
-<Weight type="chemical">215.23</Weight>
-<Weight type="physical">215.036462</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0003 AA0005">
-<Formula>C 0 H -2 N 0 O 0 S 0</Formula>
-<Weight type="chemical">-2.02</Weight>
-<Weight type="physical">-2.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sit, C.S.</Author>
-<Author>van Belkum, M.J.</Author>
-<Author>McKay, R.T.</Author>
-<Author>Worobo, R.W.</Author>
-<Author>Vederas, J.C.</Author>
-</Authors>
-<Citation>Angew. Chem. Int. Ed. Engl. 50, 8718-8721, 2011</Citation>
-<Title>The 3D solution structure of thurincin H, a bacteriocin with four sulfur to α-carbon crosslinks.</Title>
-<Xref>DOI:10.1002/anie.201102527</Xref>
-<Xref>PMID:21786372</Xref>
-<Note>mass spectrometric, (1)H-NMR, (13)C-NMR and (15)N-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sit, C.S.</Author>
-<Author>van Belkum, M.J.</Author>
-<Author>McKay, R.T.</Author>
-<Author>Worobo, R.W.</Author>
-<Author>Vederas, J.C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, April 2011</Citation>
-<Description>Thurincin H.</Description>
-<Xref>PDB:2LBZ</Xref>
-<Note>(1)H-NMR, (13)C-NMR and (15)N-NMR geometry constraint modeling; stereochemical determination</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>C, N</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:01985</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>D-amino acid</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0622.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0622.PDB" />
-</Entry>
-<Entry id="AA0623">
-<Header>
-<Code>AA0623</Code>
-<Dates>
-<CreationDate>31-Dec-2013</CreationDate>
-<StrucRevDate>31-Dec-2013</StrucRevDate>
-<TextChngDate>31-Dec-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>2-(L-cystein-S-yl)-L-serine</Name>
-<AlternateName>(2R,5R)-2,5-diamino-5-carboxy-6-hydroxy-4-thiahexanoic acid</AlternateName>
-<SystematicName>(2R)-2-amino-2-([(2R)-2-amino-2-carboxyethyl]sulfanyl)-3-hydroxypropanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 8 N 2 O 3 S 1</Formula>
-<Weight type="chemical">188.20</Weight>
-<Weight type="physical">188.025563</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0016">
-<Formula>C 0 H -2 N 0 O 0 S 0</Formula>
-<Weight type="chemical">-2.02</Weight>
-<Weight type="physical">-2.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sit, C.S.</Author>
-<Author>McKay, R.T.</Author>
-<Author>Hill, C.</Author>
-<Author>Ross, R.P.</Author>
-<Author>Vederas, J.C.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 133, 7680-7683, 2011</Citation>
-<Title>The 3D structure of thuricin CD, a two-component bacteriocin with cysteine sulfur to α-carbon cross-links.</Title>
-<Xref>DOI:10.1021/ja201802f</Xref>
-<Xref>PMID:21526839</Xref>
-<Note>(1)H-NMR, (13)C-NMR and (15)N-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sit, C.S.</Author>
-<Author>McKay, R.T.</Author>
-<Author>Hill, C.</Author>
-<Author>Ross, R.P.</Author>
-<Author>Vederas, J.C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, February 2011</Citation>
-<Description>Thurincin H.</Description>
-<Xref>PDB:2L9X</Xref>
-<Note>(1)H-NMR, (13)C-NMR and (15)N-NMR geometry constraint modeling; stereochemical determination</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>C, S</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:01986</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0623.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0623.PDB" />
-</Entry>
-<Entry id="AA0624">
-<Header>
-<Code>AA0624</Code>
-<Dates>
-<CreationDate>31-Dec-2013</CreationDate>
-<StrucRevDate>31-Dec-2013</StrucRevDate>
-<TextChngDate>31-Dec-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>2-(L-cystein-S-yl)-D-serine</Name>
-<AlternateName>(2R,5S)-2,5-diamino-5-carboxy-6-hydroxy-4-thiahexanoic acid</AlternateName>
-<SystematicName>(2S)-2-amino-2-([(2R)-2-amino-2-carboxyethyl]sulfanyl)-3-hydroxypropanoic acid</SystematicName>
-<Xref>PDBHET:DSN</Xref>
-</Names>
-<FormulaBlock>
-<Formula>C 6 H 8 N 2 O 3 S 1</Formula>
-<Weight type="chemical">188.20</Weight>
-<Weight type="physical">188.025563</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0016">
-<Formula>C 0 H -2 N 0 O 0 S 0</Formula>
-<Weight type="chemical">-2.02</Weight>
-<Weight type="physical">-2.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sit, C.S.</Author>
-<Author>van Belkum, M.J.</Author>
-<Author>McKay, R.T.</Author>
-<Author>Worobo, R.W.</Author>
-<Author>Vederas, J.C.</Author>
-</Authors>
-<Citation>Angew. Chem. Int. Ed. Engl. 50, 8718-8721, 2011</Citation>
-<Title>The 3D solution structure of thurincin H, a bacteriocin with four sulfur to α-carbon crosslinks.</Title>
-<Xref>DOI:10.1002/anie.201102527</Xref>
-<Xref>PMID:21786372</Xref>
-<Note>mass spectrometric, (1)H-NMR, (13)C-NMR and (15)N-NMR identification</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sit, C.S.</Author>
-<Author>van Belkum, M.J.</Author>
-<Author>McKay, R.T.</Author>
-<Author>Worobo, R.W.</Author>
-<Author>Vederas, J.C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, April 2011</Citation>
-<Description>Thurincin H.</Description>
-<Xref>PDB:2LBZ</Xref>
-<Note>(1)H-NMR, (13)C-NMR and (15)N-NMR geometry constraint modeling; stereochemical determination</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>C, S</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:01987</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>D-amino acid</Keyword>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0624.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0624.PDB" />
-</Entry>
-<Entry id="AA0625">
-<Header>
-<Code>AA0625</Code>
-<Dates>
-<CreationDate>31-Dec-2013</CreationDate>
-<StrucRevDate>31-Dec-2013</StrucRevDate>
-<TextChngDate>31-Dec-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>2-(L-cystein-S-yl)-L-threonine</Name>
-<AlternateName>(2R,5R,6R)-2,5-diamino-5-carboxy-6-hydroxy-4-thiaheptanoic acid</AlternateName>
-<AlternateName>alpha-(L-cystein-S-yl)-L-threonine</AlternateName>
-<SystematicName>(2R,3R)-2-amino-2-[(2R)-2-amino-2-carboxyethyl]sulfanyl-3-hydroxybutanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 7 H 10 N 2 O 3 S 1</Formula>
-<Weight type="chemical">202.23</Weight>
-<Weight type="physical">202.041213</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0017">
-<Formula>C 0 H -2 N 0 O 0 S 0</Formula>
-<Weight type="chemical">-2.02</Weight>
-<Weight type="physical">-2.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sit, C.S.</Author>
-<Author>McKay, R.T.</Author>
-<Author>Hill, C.</Author>
-<Author>Ross, R.P.</Author>
-<Author>Vederas, J.C.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 133, 7680-7683, 2011</Citation>
-<Title>The 3D structure of thuricin CD, a two-component bacteriocin with cysteine sulfur to α-carbon cross-links.</Title>
-<Xref>DOI:10.1021/ja201802f</Xref>
-<Xref>PMID:21526839</Xref>
-<Note>(1)H-NMR, (13)C-NMR and (15)N-NMR geometry constraint modeling; stereochemical determination</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sit, C.S.</Author>
-<Author>McKay, R.T.</Author>
-<Author>Hill, C.</Author>
-<Author>Ross, R.P.</Author>
-<Author>Vederas, J.C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, February 2011</Citation>
-<Description>Trn- peptide of the two-component bacteriocin thuricin CD.</Description>
-<Xref>PDB:2LBX</Xref>
-<Note>this is Trn-alpha peptide; (1)H-NMR, (13)C-NMR and (15)N-NMR geometry constraint modeling; stereochemical determination</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sit, C.S.</Author>
-<Author>McKay, R.T.</Author>
-<Author>Hill, C.</Author>
-<Author>Ross, R.P.</Author>
-<Author>Vederas, J.C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, February 2011</Citation>
-<Description>Trn- peptide of the two-component bacteriocin thuricin CD.</Description>
-<Xref>PDB:2LA0</Xref>
-<Note>this is Trn-beta peptide; (1)H-NMR, (13)C-NMR and (15)N-NMR geometry constraint modeling; stereochemical determination</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>C, T</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:01988</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0625.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0625.PDB" />
-</Entry>
-<Entry id="AA0626">
-<Header>
-<Code>AA0626</Code>
-<Dates>
-<CreationDate>31-Dec-2013</CreationDate>
-<StrucRevDate>31-Dec-2013</StrucRevDate>
-<TextChngDate>31-Dec-2013</TextChngDate>
-</Dates>
-</Header>
-<Names>
-<Name>2-(L-cystein-S-yl)-D-tyrosine</Name>
-<AlternateName>(2R,5S)-2,5-diamino-5-carboxyl-6-(hydroxyphenyl)-4-thiahexanoic acid</AlternateName>
-<AlternateName>alpha-(L-cystein-S-yl)-D-tyrosine</AlternateName>
-<SystematicName>(2S)-2-amino-2-([(2R)-2-amino-2-carboxyethyl]sulfanyl)-3-(4-hydroxyphenyl)propanoic acid</SystematicName>
-</Names>
-<FormulaBlock>
-<Formula>C 12 H 12 N 2 O 3 S 1</Formula>
-<Weight type="chemical">264.30</Weight>
-<Weight type="physical">264.056863</Weight>
-</FormulaBlock>
-<CorrectionBlock uids="AA0005 AA0019">
-<Formula>C 0 H -2 N 0 O 0 S 0</Formula>
-<Weight type="chemical">-2.02</Weight>
-<Weight type="physical">-2.015650</Weight>
-</CorrectionBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sit, C.S.</Author>
-<Author>McKay, R.T.</Author>
-<Author>Hill, C.</Author>
-<Author>Ross, R.P.</Author>
-<Author>Vederas, J.C.</Author>
-</Authors>
-<Citation>J. Am. Chem. Soc. 133, 7680-7683, 2011</Citation>
-<Title>The 3D structure of thuricin CD, a two-component bacteriocin with cysteine sulfur to α-carbon cross-links.</Title>
-<Xref>DOI:10.1021/ja201802f</Xref>
-<Xref>PMID:21526839</Xref>
-<Note>(1)H-NMR, (13)C-NMR and (15)N-NMR geometry constraint modeling; stereochemical determination</Note>
-</ReferenceBlock>
-<ReferenceBlock>
-<Authors>
-<Author>Sit, C.S.</Author>
-<Author>McKay, R.T.</Author>
-<Author>Hill, C.</Author>
-<Author>Ross, R.P.</Author>
-<Author>Vederas, J.C.</Author>
-</Authors>
-<Citation type="submission">submitted to the Protein Data Bank, February 2011</Citation>
-<Description>Trn- peptide of the two-component bacteriocin thuricin CD.</Description>
-<Xref>PDB:2LA0</Xref>
-<Note>this is Trn-beta peptide; (1)H-NMR, (13)C-NMR and (15)N-NMR geometry constraint modeling; stereochemical determination</Note>
-</ReferenceBlock>
-<SequenceCode>
-<SequenceSpec>C, Y</SequenceSpec>
-<Condition>cross-link 2</Condition>
-<Xref>PSI-MOD:01989</Xref>
-</SequenceCode>
-<Source>natural</Source>
-<Keywords>
-<Keyword>thioether bond</Keyword>
-</Keywords>
-<Features>
-<FeatureNote>
-<Feature type="UniProt">Not available</Feature>
-<Note>this modification is not annotated in UniProt features</Note>
-</FeatureNote>
-</Features>
-<Image src="/images/AA0626.GIF" alt="DUMMY.GIF" />
-<Model src="/models/AA0626.PDB" />
-</Entry>
-</Database>
diff --git a/rustyms-generate-databases/data/XLMOD.obo b/rustyms-generate-databases/data/XLMOD.obo
deleted file mode 100644
index 1fc3f3a2..00000000
--- a/rustyms-generate-databases/data/XLMOD.obo
+++ /dev/null
@@ -1,10313 +0,0 @@
-format-version: 1.2
-data-version: release/2019-10-28
-ontology: xlmod
-date: 23:03:2021 20:08
-saved-by: Paul Thomas
-auto-generated-by: OBO-Edit 2.3.1
-default-namespace: XLMOD
-remark: version: 1.1.12
-remark: coverage: cross-linking reagents, cross-linker related post-translational modifications, and derivatization reagents for GC-MS and LC-MS
-remark: creator: Lutz Fischer <lfischer <-at-> staffmail.ed.ac.uk>
-remark: creator: Alexander Leitner <leitner <-at-> imsb.biol.ethz.ch>
-remark: creator: Nils Hoffmann <nils.hoffmann <-at-> isas.de>
-remark: creator: Gerhard Mayer <mayerg97 <-at-> rub.de>
-remark: This work is licensed under the Creative Commons Attribution 4.0 International (CC BY 4.0) license.
-remark: To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/ or send a letter to Creative Commons, 444 Castro Street, Suite 900, Mountain View, California, 94041, USA.
-
-[Typedef]
-id: part_of
-name: part_of
-is_transitive: true
-def: "The basic part of relationship indicating a top-level branch of this ontology." [OBO:defs]
-
-[Typedef]
-id: is_activatable
-name: is_activatable
-def: "Indicates how the cross-linking reagent can be activated." [OBO:defs]
-
-[Typedef]
-id: is_analog_of
-name: is_analog_of
-def: "Indicates biochemical analogues of nucleobases, nucleosides or amino acids." [OBO:defs]
-
-[Typedef]
-id: is_cleavable
-name: is_cleavable
-def: "Indicates that the cross-linking reagent is cleavable." [OBO:defs]
-
-[Typedef]
-id: is_labelled
-name: is_labelled
-def: "Indicates that the cross-linking or derivatization reagent has an isotopic label." [OBO:defs]
-
-[Typedef]
-id: is_partially_reacted
-name: is_partially_reacted
-def: "Specifies the type of the cross-linker related chemical modification." [OBO:defs]
-
-[Typedef]
-id: is_reactive_with
-name: is_reactive_with
-def: "Indicates the chemical group that can react with the cross-linking or derivatization reagent." [OBO:defs]
-
-[Typedef]
-id: is_side_product_of
-name: is_side_product_of
-def: "Indicates the cross-linking reagent from which the chemical modification is derived." [OBO:defs]
-
-[Typedef]
-id: has_handle
-name: has_handle
-def: "Indicates that the cross-linking reagent has a handle that can be used for detection/identification, enrichment or purification." [OBO:defs]
-
-[Typedef]
-id: has_click_enabled_linker
-name: has_click_enabled_linker
-def: "Indicates that the cross-linking reagent has a linker that can be enabled by click chemistry." [OBO:defs]
-
-[Typedef]
-id: has_neutral_loss_reporter
-name: has_neutral_loss_reporter
-def: "Indicates that the cross-linking reagent has a neutral loss reporter." [OBO:defs]
-
-[Typedef]
-id: has_property
-name: has_property
-def: "Indicates a property of a cross-linking or derivatization reagent." [OBO:defs]
-
-[Typedef]
-id: has_chromophore
-name: has_chromophore
-def: "Indicates that the derivatization reagent can be detected by the specified chromophore." [OBO:defs]
-
-[Typedef]
-id: has_electrophore
-name: has_electrophore
-def: "Indicates that the derivatization reagent can be detected by the specified electrophore." [OBO:defs]
-
-[Typedef]
-id: has_fluorophore
-name: has_fluorophore
-def: "Indicates that the derivatization reagent can be detected by the specified fluorophore." [OBO:defs]
-
-[Typedef]
-id: has_reactive_group
-name: has_reactive_group
-def: "Indicates that the cross-linking or derivatization reagent has the specified reactive group." [OBO:defs]
-
-[Term]
-id: XLMOD:00000
-name: Proteomics Standards Initiative cross-linking and derivatization controlled vocabulary
-def: "Proteomics Standards Initiative cross-linking and derivatization controlled vocabulary." [PSI:XL]
-
-[Term]
-id: XLMOD:00001
-name: cross-linking entity
-def: "Entity relevant to the domain of cross-linking in proteomics." [PSI:XL]
-relationship: part_of XLMOD:00000 ! Proteomics Standards Initiative cross-linking and derivatization controlled vocabulary
-
-[Term]
-id: XLMOD:00002
-name: cross-linker related chemical modification
-def: "Dead-end modification resulting from a cross-linker reagent reacting only with one peptide." [PSI:XL]
-relationship: part_of XLMOD:00000 ! Proteomics Standards Initiative cross-linking and derivatization controlled vocabulary
-
-[Term]
-id: XLMOD:00003
-name: label transfer reagent
-def: "A cross-linker acting as label transfer reagent." [PSI:XL]
-relationship: part_of XLMOD:00000 ! Proteomics Standards Initiative cross-linking and derivatization controlled vocabulary
-
-[Term]
-id: XLMOD:00004
-name: cross-linker
-def: "Compound that can link two or more polymer chains." [PSI:XL]
-is_a: XLMOD:00001 ! cross-linking entity
-
-[Term]
-id: XLMOD:00005
-name: homofunctional cross-linker
-def: "A cross-linking reagent with identical reactive groups at each end of the spacer arm." [PSI:XL]
-is_a: XLMOD:00004 ! cross-linker
-
-[Term]
-id: XLMOD:00006
-name: heterofunctional cross-linker
-def: "A cross-linking reagent with at least two different reactive groups." [PSI:XL]
-is_a: XLMOD:00004 ! cross-linker
-
-[Term]
-id: XLMOD:00007
-name: photoreactive cross-linker
-def: "OBSOLETE A cross-linking reagent that becomes reactive when exposed to ultraviolet or visible light." [PSI:XL]
-comment: This term was made obsolete because photo-reactivity is now encoded for the reactive groups of the cross-linkers, see (XLMOD:00108).
-is_obsolete: true
-
-[Term]
-id: XLMOD:00008
-name: zero-length cross-linker
-def: "A cross-linking reagent causing direct conjugation without becoming part of the final cross-link between the target molecules." [PSI:XL]
-is_a: XLMOD:00004 ! cross-linker
-
-[Term]
-id: XLMOD:00009
-name: cross-linking attribute
-def: "An attribute describing a cross-linker." [PSI:XL]
-is_a: XLMOD:00001 ! cross-linking entity
-
-[Term]
-id: XLMOD:00010
-name: deuterium labelled
-def: "Indicates that a cross-linker is deuterium labelled." [PSI:XL]
-is_a: XLMOD:00009 ! cross-linking attribute
-
-[Term]
-id: XLMOD:00011
-name: hydrolyzed
-def: "Indicates that a cross-linker is hydrolyzed, for example for NHS-type reagents -C(=O)-NHS was converted to -C(=O)-OH." [PSI:XL]
-is_a: XLMOD:00009 ! cross-linking attribute
-
-[Term]
-id: XLMOD:00012
-name: amidated
-def: "Indicates that a cross-linker is amidated." [PSI:XL]
-is_a: XLMOD:00009 ! cross-linking attribute
-
-[Term]
-id: XLMOD:00013
-name: membrane permeable
-def: "Indicates that a cross-linker is membrane permeable." [PSI:XL]
-is_a: XLMOD:00009 ! cross-linking attribute
-
-[Term]
-id: XLMOD:00014
-name: hydrophilic
-def: "Indicates that a cross-linker is hydrophilic." [PSI:XL]
-is_a: XLMOD:00009 ! cross-linking attribute
-
-[Term]
-id: XLMOD:00015
-name: fluorescent
-def: "Indicates that a cross-linker is fluorescent." [PSI:XL]
-is_a: XLMOD:00009 ! cross-linking attribute
-
-[Term]
-id: XLMOD:00016
-name: cleavable
-def: "Indicates that a cross-linker is cleavable." [PSI:XL]
-is_a: XLMOD:00009 ! cross-linking attribute
-
-[Term]
-id: XLMOD:00017
-name: chemically cleavable
-def: "Indicates that a cross-linker is chemically cleavable." [PSI:XL]
-is_a: XLMOD:00016 ! cleavable
-
-[Term]
-id: XLMOD:00018
-name: cleavable by MS2 labile bond
-def: "Indicates that a cross-linker is mass-spectrometrically cleavable, i.e. contains a MS2 labile bond leading to fragments detected in MS3." [PSI:XL]
-is_a: XLMOD:00016 ! cleavable
-
-[Term]
-id: XLMOD:00019
-name: enrichable
-def: "Indicates that a cross-linker facilitates enrichment." [PSI:XL]
-is_a: XLMOD:00009 ! cross-linking attribute
-
-[Term]
-id: XLMOD:00020
-name: iodinatable
-def: "Indicates that a cross-linker is iodinatable, e.g. for autoradiographic detection by radio-labelling with J-131." [PSI:XL]
-is_a: XLMOD:00009 ! cross-linking attribute
-
-[Term]
-id: XLMOD:00021
-name: ammonium amidated
-def: "Indicates a dead-end modification that was amidated by an ammonium salt, like e.g. bicarbonate, phosphate, chloride, for example for NHS-type reagents -C(=O)-NHS was converted to -C(=O)-NH2." [PSI:XL]
-is_a: XLMOD:00012 ! amidated
-
-[Term]
-id: XLMOD:00022
-name: Tris amidated
-def: "Indicates a dead-end modification that was amidated by Tris(hydroxymethyl)-aminomethane, for example for NHS-type reagents -C(=O)-NHS was converted to -C(=O)-NHC(CH2OH)3." [PSI:XL]
-is_a: XLMOD:00012 ! amidated
-
-[Term]
-id: XLMOD:00023
-name: cleavable S-S bond
-def: "Indicates that a cross-linker contains a cleavable S-S bond, which is chemically cleavable by reducing agents like e.g. thiols, beta-mercaptoethanol, dithiothreitol (DTT), mercaptomethylamine or Tris(2-carboxyethyl)phosphin (TCEP)." [PSI:XL]
-is_a: XLMOD:00017 ! chemically cleavable
-relationship: is_cleavable XLMOD:00041 ! thiol cleavable
-relationship: is_cleavable XLMOD:00038 ! DTT cleavable
-relationship: is_cleavable XLMOD:00042 ! TCEP cleavable
-relationship: is_cleavable XLMOD:00043 ! mercaptoethanol cleavable
-
-[Term]
-id: XLMOD:00024
-name: periodate cleavable
-def: "Indicates that a cross-linker is chemically cleavable by the oxidizing agent periodate." [PSI:XL]
-is_a: XLMOD:00017 ! chemically cleavable
-
-[Term]
-id: XLMOD:00025
-name: hydroxylamine cleavable
-def: "Indicates that a cross-linker is chemically cleavable by hydroxylamine." [PSI:XL]
-is_a: XLMOD:00017 ! chemically cleavable
-
-[Term]
-id: XLMOD:00026
-name: reactive group attribute
-def: "An attribute describing a reactive group." [PSI:XL]
-relationship: part_of XLMOD:00001 ! cross-linking entity
-
-[Term]
-id: XLMOD:00027
-name: chemically reactive
-def: "Indicates that a reactive group reacts with specific functional groups." [PSI:XL]
-is_a: XLMOD:00026 ! reactive group attribute
-
-[Term]
-id: XLMOD:00028
-name: primary amine reactive
-def: "Indicates that a reactive group is reactive with primary amino (-NH2) groups." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:00029
-name: sulfhydryl reactive
-def: "Indicates that a reactive group is reactive with sulfhydryl (-SH) groups." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:00030
-name: carboxyl reactive
-def: "Indicates that a reactive group is reactive with carboxyl (-COOH) groups." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:00031
-name: aldehyde reactive
-def: "Indicates that a reactive group is reactive with aldehyde (-CHO) or carbonyl (-CO) groups." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:00032
-name: hydroxyl reactive
-def: "Indicates that a reactive group is reactive with hydroxyl (-OH) groups." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:00033
-name: azide reactive
-def: "Indicates that a reactive group is reactive with azide (-N3) groups." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:00034
-name: photo cleavable
-def: "Indicates that a cross-linker is cleavable by light." [PSI:XL]
-is_a: XLMOD:00016 ! cleavable
-
-[Term]
-id: XLMOD:00035
-name: CID cleavable
-def: "Indicates that a cross-linker is mass-spectrometrically cleavable by collission induced dissociation." [PSI:XL]
-is_a: XLMOD:00016 ! cleavable
-
-[Term]
-id: XLMOD:00036
-name: 13C labelled
-def: "Indicates that a cross-linker is labelled with carbon-13." [PSI:XL]
-is_a: XLMOD:00009 ! cross-linking attribute
-
-[Term]
-id: XLMOD:00037
-name: non-selective
-def: "Indicates that a cross-linker is non-selective (i.e. can react with different amino acids, but also with DNA/RNA and carbohydrates (aldehyde reactive))." [PSI:XL]
-is_a: XLMOD:00026 ! reactive group attribute
-
-[Term]
-id: XLMOD:00038
-name: DTT cleavable
-def: "Indicates that a cross-linker is chemically cleavable by the reducing agent DTT (dithiothreitol)." [PSI:XL]
-is_a: XLMOD:00017 ! chemically cleavable
-
-[Term]
-id: XLMOD:00039
-name: ammonium cleavable
-def: "Indicates that a cross-linker is chemically cleavable by ammonium hydroxide." [PSI:XL]
-is_a: XLMOD:00017 ! chemically cleavable
-
-[Term]
-id: XLMOD:00040
-name: ISD cleavable
-def: "Indicates that a cross-linker is mass-spectrometrically cleavable by in-source decay." [PSI:XL]
-is_a: XLMOD:00016 ! cleavable
-
-[Term]
-id: XLMOD:00041
-name: thiol cleavable
-def: "Indicates that a cross-linker is mass-spectrometrically cleavable (reducible) by thiols." [PSI:XL]
-synonym: "DTT cleavable" RELATED []
-synonym: "TCEP cleavable" RELATED []
-synonym: "mercaptoethanol cleavable" RELATED []
-is_a: XLMOD:00016 ! cleavable
-
-[Term]
-id: XLMOD:00042
-name: TCEP cleavable
-def: "Indicates that a cross-linker is chemically cleavable by the reducing agent TCEP (Tris(2-carboxyethyl)phosphin)." [PSI:XL]
-is_a: XLMOD:00017 ! chemically cleavable
-
-[Term]
-id: XLMOD:00043
-name: mercaptoethanol cleavable
-def: "Indicates that a cross-linker is chemically cleavable by the reducing agent mercaptoethanol." [PSI:XL]
-is_a: XLMOD:00017 ! chemically cleavable
-
-[Term]
-id: XLMOD:00044
-name: mass defect labelled
-def: "Indicates that a cross-linker is mass defect labelled." [PSI:XL]
-is_a: XLMOD:00009 ! cross-linking attribute
-
-[Term]
-id: XLMOD:00045
-name: thioether reactive
-def: "Indicates that a reactive group is reactive with thioether (R1-S-R2) groups." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:00046
-name: imidazole reactive
-def: "Indicates that a reactive group is reactive with the heterocyclic imidazole groups." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:00047
-name: thioesterized
-def: "Indicates that a cross-linker is thioesterized." [PSI:XL]
-is_a: XLMOD:00009 ! cross-linking attribute
-
-[Term]
-id: XLMOD:00048
-name: nucleic acid reactive
-def: "Indicates that a reactive group is reactive with RNA or DNA." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:00049
-name: amino acid derivative
-def: "An amino acid derivative used in cross-linking experiments." [PSI:XL]
-is_a: XLMOD:00001 ! cross-linking entity
-
-[Term]
-id: XLMOD:00050
-name: handle
-def: "A handle attached to a cross-linker used for detection, affinity enrichment or purification." [PSI:XL]
-is_a: XLMOD:00001 ! cross-linking entity
-relationship: part_of XLMOD:00004 ! cross-linker
-
-[Term]
-id: XLMOD:00051
-name: biotin
-def: "A Biotin affinity handle, enrichable with avidin, streptavidin or neutravidin, attached to a cross-linker." [PSI:XL]
-is_a: XLMOD:00050 ! handle
-is_a: XLMOD:00019 ! enrichable
-
-[Term]
-id: XLMOD:00052
-name: NO2 neutral loss reporter
-def: "A NO2 detection tag." [PMID:19496583]
-is_a: XLMOD:00050 ! handle
-
-[Term]
-id: XLMOD:00053
-name: alkyne
-def: "An alkyne (hadrocarbon with at least one C-C triple bond) tag, e.g. BARAC (biarylazacycloctynone) to enable enrichment of cross-linked peptides by either coupling of an affinity group with alkyne-azido click chemistry or by using immobilized azide linkers." [PMID:19496583]
-is_a: XLMOD:00050 ! handle
-is_a: XLMOD:00019 ! enrichable
-
-[Term]
-id: XLMOD:00054
-name: DNB
-def: "A dinitrobenzole affinity handle for enrichment with anti-DNB antibodies, attached to a cross-linker." [PSI:XL]
-is_a: XLMOD:00050 ! handle
-is_a: XLMOD:00019 ! enrichable
-
-[Term]
-id: XLMOD:00055
-name: azide
-def: "A photoreactive azide (-N3) tag to enable enrichment of cross-linked peptides with either immobilized alkyne linkers or by azide-alkyne click chemistry using biotin-alkyne respective biotin-phosphine." [PMID:20472459]
-is_a: XLMOD:00050 ! handle
-is_a: XLMOD:00019 ! enrichable
-is_a: XLMOD:00100 ! reactive group
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-relationship: is_reactive_with XLMOD:00037 ! non-selective
-
-[Term]
-id: XLMOD:00056
-name: CHCA
-def: "An alpha-cyano-4-hydroxycinnamic acid UV-absorbing label for signal enhancement." [PMID:19902427]
-is_a: XLMOD:00050 ! handle
-
-[Term]
-id: XLMOD:00057
-name: generic neutral loss reporter
-def: "A generic neutral loss reporter." [PXI:XL]
-is_a: XLMOD:00050 ! handle
-
-[Term]
-id: XLMOD:00058
-name: amino acid
-def: "An amino acid compound." [PSI:XL]
-is_a: XLMOD:00001 ! cross-linking entity
-
-[Term]
-id: XLMOD:00059
-name: L-Leucine
-def: "The amino acid L-Leucine." [PXI:XL]
-is_a: XLMOD:00058 ! amino acid
-
-[Term]
-id: XLMOD:00060
-name: L-Methionine
-def: "The amino acid L-Methionine." [PXI:XL]
-is_a: XLMOD:00058 ! amino acid
-
-[Term]
-id: XLMOD:00061
-name: base cleavable
-def: "Indicates that a cross-linker is chemically cleavable by bases." [PSI:XL]
-is_a: XLMOD:00017 ! chemically cleavable
-
-[Term]
-id: XLMOD:00062
-name: hydrazine reactive
-def: "Indicates that a reactive group is reactive with hydrazines (N2H4)." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:00063
-name: carbonyl reactive
-def: "Indicates that a reactive group is reactive with carbonyl (R1-CO-R2) groups." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:00064
-name: oxidized
-def: "Indicates that a cross-linker is oxidized, e.g. by oxidizing a carbonyl to a carboxyl functional group." [PSI:XL]
-is_a: XLMOD:00009 ! cross-linking attribute
-
-[Term]
-id: XLMOD:00065
-name: alkenized
-def: "Indicates that a cross-linker is modified to it's alkene form (loss of two hydrogen atoms by forming a C=C double bond)." [PSI:XL]
-is_a: XLMOD:00009 ! cross-linking attribute
-
-[Term]
-id: XLMOD:00066
-name: acid cleavable
-def: "Indicates that a cross-linker is chemically cleavable by acids." [PSI:XL]
-is_a: XLMOD:00017 ! chemically cleavable
-
-[Term]
-id: XLMOD:00067
-name: CID cleavable C-S bond
-def: "Indicates that a cross-linker contains a CID (Collision Induced Dissociation) cleavable C-S bond." [PSI:XL]
-is_a: XLMOD:00035 ! CID cleavable
-relationship: is_cleavable XLMOD:00018 ! cleavable by MS2 labile bond
-
-[Term]
-id: XLMOD:00068
-name: L-Isoleucine
-def: "The amino acid L-Isoleucine." [PXI:XL]
-is_a: XLMOD:00058 ! amino acid
-
-[Term]
-id: XLMOD:00069
-name: 18O labelled
-def: "Indicates that a cross-linker is labelled with oxygen-18." [PSI:XL]
-is_a: XLMOD:00009 ! cross-linking attribute
-
-[Term]
-id: XLMOD:00070
-name: L-Phenylalanine
-def: "The amino acid L-Phenylalanine." [PXI:XL]
-is_a: XLMOD:00058 ! amino acid
-
-[Term]
-id: XLMOD:00071
-name: iminobiotintrifluoroacetamide
-def: "A Iminobiotin trifluoroacetamide affinity handle, enrichable with avidin, streptavidin or neutravidin, attached to a cross-linker." [PSI:XL]
-is_a: XLMOD:00050 ! handle
-is_a: XLMOD:00019 ! enrichable
-relationship: is_reactive_with XLMOD:00072 ! avidin reactive
-
-[Term]
-id: XLMOD:00072
-name: avidin reactive
-def: "Indicates that a reactive group is reactive with either of the glycoproteins avidin, streptavidin or neutravidin." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:00073
-name: nucleobase
-def: "A nitrogeneous base occurring in nucleic acids." [PSI:XL]
-is_a: XLMOD:00001 ! cross-linking entity
-
-[Term]
-id: XLMOD:00074
-name: purine base
-def: "A purine base occurring in nucleic acids." [PSI:XL]
-is_a: XLMOD:00073 ! nucleobase
-
-[Term]
-id: XLMOD:00075
-name: pyrimidine base
-def: "A pyrimidine base occurring in nucleic acids." [PSI:XL]
-is_a: XLMOD:00073 ! nucleobase
-
-[Term]
-id: XLMOD:00076
-name: adenine
-def: "The nucleobase adenine." [PXI:XL]
-is_a: XLMOD:00074 ! purine base
-
-[Term]
-id: XLMOD:00077
-name: guanine
-def: "The nucleobase guanine." [PXI:XL]
-is_a: XLMOD:00074 ! purine base
-
-[Term]
-id: XLMOD:00078
-name: cytosine
-def: "The nucleobase cytosine." [PXI:XL]
-is_a: XLMOD:00075 ! pyrimidine base
-
-[Term]
-id: XLMOD:00079
-name: thymine
-def: "The nucleobase thymine." [PXI:XL]
-is_a: XLMOD:00075 ! pyrimidine base
-
-[Term]
-id: XLMOD:00080
-name: uracil
-def: "The nucleobase uracil." [PXI:XL]
-is_a: XLMOD:00075 ! pyrimidine base
-
-[Term]
-id: XLMOD:00081
-name: nucleobase derivative
-def: "A nucleobase derivative used in cross-linking experiments for protein-oligonucleotide cross-linking." [PSI:XL]
-is_a: XLMOD:00001 ! cross-linking entity
-relationship: is_analog_of XLMOD:00073 ! nucleobase
-
-[Term]
-id: XLMOD:00082
-name: nucleoside
-def: "A combination of a nucleobase and a sugar (either ribose or deoxyribose)." [PSI:XL]
-is_a: XLMOD:00001 ! cross-linking entity
-
-[Term]
-id: XLMOD:00083
-name: adenosine
-def: "The nucleoside adenosine." [PXI:XL]
-is_a: XLMOD:00082 ! nucleoside
-
-[Term]
-id: XLMOD:00084
-name: guanosine
-def: "The nucleoside guanosine." [PXI:XL]
-is_a: XLMOD:00082 ! nucleoside
-
-[Term]
-id: XLMOD:00085
-name: cytidine
-def: "The nucleoside cytidine." [PXI:XL]
-is_a: XLMOD:00082 ! nucleoside
-
-[Term]
-id: XLMOD:00086
-name: uridine
-def: "The nucleoside uridine." [PXI:XL]
-is_a: XLMOD:00082 ! nucleoside
-
-[Term]
-id: XLMOD:00087
-name: 5-methyluridine
-def: "The nucleoside 5-methyluridine." [PXI:XL]
-is_a: XLMOD:00082 ! nucleoside
-
-[Term]
-id: XLMOD:00088
-name: nucleoside derivative
-def: "A nucleoside derivative used in cross-linking experiments for protein-oligonucleotide cross-linking." [PSI:XL]
-is_a: XLMOD:00001 ! cross-linking entity
-relationship: is_analog_of XLMOD:00082 ! nucleoside
-
-[Term]
-id: XLMOD:00089
-name: RNA-SH
-def: "Thiol-modified RNA." [PSI:XL]
-is_a: XLMOD:00001 ! cross-linking entity
-
-[Term]
-id: XLMOD:00090
-name: biotin-alkyne
-def: "A biotin-alkyne affinity handle, which can be used for enrichment with click-chemistry." [PSI:XL]
-is_a: XLMOD:00050 ! handle
-is_a: XLMOD:00019 ! enrichable
-relationship: is_reactive_with XLMOD:00033 ! azide reactive
-
-[Term]
-id: XLMOD:00091
-name: tetramethylrhodamine-alkyne
-def: "A tetramethylrhodamine-alkyne affinity handle, which can be used for enrichment with click-chemistry." [PSI:XL]
-synonym: "TAMRA" EXACT []
-is_a: XLMOD:00050 ! handle
-is_a: XLMOD:00019 ! enrichable
-relationship: is_reactive_with XLMOD:00033 ! azide reactive
-
-[Term]
-id: XLMOD:00092
-name: lipid analogue
-def: "A lipid analogue used in cross-linking experiments for lipid-protein cross-linking." [PSI:XL]
-is_a: XLMOD:00001 ! cross-linking entity
-
-[Term]
-id: XLMOD:00093
-name: sialic acid analogue
-def: "A sialic acid analogue used in cross-linking experiments for glycan-protein cross-linking." [PSI:XL]
-is_a: XLMOD:00001 ! cross-linking entity
-
-[Term]
-id: XLMOD:00094
-name: alkenized cross-linker related chemical modification
-def: "Alkenization dead-end modification resulting from a cross-linker reagent reacting only with one peptide." [PSI:XL]
-is_a: XLMOD:00002 ! cross-linker related chemical modification
-
-[Term]
-id: XLMOD:00095
-name: ammonium amidation cross-linker related chemical modification
-def: "Ammonium amidation dead-end modification resulting from a cross-linker reagent reacting only with one peptide." [PSI:XL]
-is_a: XLMOD:00002 ! cross-linker related chemical modification
-
-[Term]
-id: XLMOD:00096
-name: hydrolization cross-linker related chemical modification
-def: "Hydrolization dead-end modification resulting from a cross-linker reagent reacting only with one peptide." [PSI:XL]
-is_a: XLMOD:00002 ! cross-linker related chemical modification
-
-[Term]
-id: XLMOD:00097
-name: oxidation cross-linker related chemical modification
-def: "Oxidition dead-end modification resulting from a cross-linker reagent reacting only with one peptide." [PSI:XL]
-is_a: XLMOD:00002 ! cross-linker related chemical modification
-
-[Term]
-id: XLMOD:00098
-name: thioesterization cross-linker related chemical modification
-def: "Thio-esterization dead-end modification resulting from a cross-linker reagent reacting only with one peptide." [PSI:XL]
-is_a: XLMOD:00002 ! cross-linker related chemical modification
-
-[Term]
-id: XLMOD:00099
-name: formic acid cleavable
-def: "Indicates that a cross-linker is chemically cleavable by formic acid." [PSI:XL]
-is_a: XLMOD:00017 ! chemically cleavable
-
-[Term]
-id: XLMOD:00100
-name: reactive group
-def: "Part of a cross-linker that reacts with the amino-acids of the protein." [PSI:XL]
-is_a: XLMOD:00009 ! cross-linking attribute
-
-[Term]
-id: XLMOD:00101
-name: NHS ester
-def: "A reactive group (N-hydroxysuccinimide) that reacts with lysines and N-termini but also serines, threonines and tyrosines." [PSI:XL]
-synonym: "N-hydroxysuccinimide ester" EXACT []
-property_value: specificities: "(K,Protein N-term)" xsd:string
-property_value: secondarySpecificities: "(S,T,Y)" xsd:string
-is_a: XLMOD:00100 ! reactive group
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:00102
-name: Sulfo NHS ester
-def: "A reactive group (N-hydroxysulfosuccinimide) that reacts with lysines and N-termini but also serines, threonines and tyrosines." [PSI:XL]
-synonym: "N-hydroxysulfosuccinimide ester" EXACT []
-property_value: specificities: "(K,Protein N-term)" xsd:string
-property_value: secondarySpecificities: "(S,T,Y)" xsd:string
-is_a: XLMOD:00100 ! reactive group
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:00103
-name: diazirine
-def: "Photoreactive group (R1-CN2-R2) that inserts into any C-H or N-H bond." [PSI:XL]
-property_value: waveLengthRange: "330-370 nm" xsd:string
-is_a: XLMOD:00100 ! reactive group
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-relationship: is_reactive_with XLMOD:00037 ! non-selective
-
-[Term]
-id: XLMOD:00104
-name: N-hydroxyphthalimide
-def: "A reactive group that reacts with amines." [PMID:19994840]
-property_value: specificities: "(K,N,Q,R,Protein N-term)" xsd:string
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:00105
-name: carbodiimide
-def: "A Carboxyl-to-amine (R1-N=C=N_R2) reactive chemical group." [PSI:XL]
-property_value: specificities: "(K,N,Q,R,Protein N-term)&(E,D,Protein C-term)" xsd:string
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:00106
-name: maleimide
-def: "A reactive group that reacts with sulfhydryl groups." [PSI:XL]
-property_value: specificities: "(C)" xsd:string
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00029 ! sulfhydryl reactive
-
-[Term]
-id: XLMOD:00107
-name: nitrophenyl azide
-def: "A nitrophenyl azide photoreactive group." [PSI:XL]
-property_value: waveLengthRange: "320-370 nm" xsd:string
-is_a: XLMOD:00114 ! aryl azide
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-relationship: is_reactive_with XLMOD:00037 ! non-selective
-relationship: is_reactive_with XLMOD:00089 ! RNA-SH
-
-[Term]
-id: XLMOD:00108
-name: photoreactive
-def: "Indicates that a reactive group is photoreactive." [PSI:XL]
-is_a: XLMOD:00026 ! reactive group attribute
-
-[Term]
-id: XLMOD:00109
-name: pyridinyldisulfide
-def: "A pyridinyldisulfide reactive group that reacts with sulfhydryl groups to form disulfide bonds." [PSI:XL]
-synonym: "pyridyl disulfide" EXACT []
-synonym: "pyridyldithiol" EXACT []
-property_value: specificities: "(C)" xsd:string
-is_a: XLMOD:00100 ! reactive group
-relationship: is_cleavable XLMOD:00023 ! cleavable S-S bond
-relationship: is_reactive_with XLMOD:00029 ! sulfhydryl reactive
-
-[Term]
-id: XLMOD:00110
-name: hydrazide
-def: "A hydrazide reactive group (-CO-NH-NH2) that reacts with carbonyls to form hydrazone bonds." [PSI:XL]
-property_value: specificities: "(D,E,Protein C-term)" xsd:string
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-relationship: is_reactive_with XLMOD:00031 ! aldehyde reactive
-relationship: is_reactive_with XLMOD:06510 ! ketone reactive
-
-[Term]
-id: XLMOD:00111
-name: imidoester
-def: "An amine-reactive chemical group (R1-C(=NH)-OR2)." [PSI:XL]
-property_value: specificities: "(K,N,Q,R,Protein N-term)" xsd:string
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:00112
-name: haloacetyl
-def: "A reactive group (alpha-haloacetyl, halo-C2H5), mostly a iodoacetyl, bromoacetyl or chloroacetyl group, that reacts with sulfhydryl groups." [PSI:XL]
-property_value: specificities: "(C)" xsd:string
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00029 ! sulfhydryl reactive
-
-[Term]
-id: XLMOD:00113
-name: alkoxyamine
-def: "A reactive group (R-O-N-R2) that conjugates to carbonyls." [PSI:XL]
-property_value: specificities: "(D,E,Protein C-term)" xsd:string
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00031 ! aldehyde reactive
-
-[Term]
-id: XLMOD:00114
-name: aryl azide
-def: "Photoreactive aryl(Ar)-substitited azide (N=N=N) group, that initiates addition reactions with double bonds or insertion into C-H and N-H bonds or reacts with primary amines." [PSI:XL]
-property_value: waveLengthRange: "250-350 nm" xsd:string
-is_a: XLMOD:00055 ! azide
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:00037 ! non-selective
-
-[Term]
-id: XLMOD:00115
-name: glyoxal
-def: "An arginine-specific reactive group (H-CO-CO-H)." [PSI:XL]
-property_value: baseSpecificities: "(Guanine)" xsd:string
-property_value: specificities: "(R)" xsd:string
-is_a: XLMOD:00100 ! reactive group
-
-[Term]
-id: XLMOD:00116
-name: aldehyde group
-def: "An aldehyde (R-CO-H) reactive group." [PSI:XL]
-property_value: specificities: "(K,N,R,Q,Y,Protein N-term)" xsd:string
-property_value: secondarySpecificities: "(C,F,H,S,T,W)" xsd:string
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:00117
-name: acryl
-def: "A reactive group (CH2=CH-CO-R) that reacts with sulfhydryl (-SH) groups." [PMID:22641729]
-property_value: specificities: "(C)" xsd:string
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00029 ! sulfhydryl reactive
-
-[Term]
-id: XLMOD:00118
-name: tetrafluorophenyl azide
-def: "Tetrafluorophenyl (TFP) azide (N=N=N) photoreactive group." [PMID:22641729]
-is_a: XLMOD:00114 ! aryl azide
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-relationship: is_reactive_with XLMOD:00037 ! non-selective
-
-[Term]
-id: XLMOD:00119
-name: benzophenone
-def: "Benzophenone photoreactive group." [PMID:22641729]
-property_value: waveLengthRange: "350-360 nm" xsd:string
-is_a: XLMOD:00100 ! reactive group
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-relationship: is_reactive_with XLMOD:00037 ! non-selective
-relationship: is_reactive_with XLMOD:00089 ! RNA-SH
-
-[Term]
-id: XLMOD:00120
-name: pentafluorophenyl
-def: "A reactive group (F5-Ph) that reacts with amines." [PMID:22067100]
-synonym: "PFP ester" EXACT []
-property_value: specificities: "(K,N,Q,R,Protein N-term)" xsd:string
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:00121
-name: methanethiosulfonate
-def: "A reactive group (Ch3-SO2-S-R) that reacts with sulfhydryl (-SH) groups." [PSI:XL]
-synonym: "MTS" EXACT []
-property_value: specificities: "(C)" xsd:string
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00029 ! sulfhydryl reactive
-
-[Term]
-id: XLMOD:00122
-name: 4-azido-2,3,5,6-tetrafluorobenzene
-def: "Photoreactive group that inserts into any C-H bond." [PSI:XL]
-synonym: "ATFB" EXACT []
-property_value: waveLengthRange: "UV" xsd:string
-is_a: XLMOD:00100 ! reactive group
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-relationship: is_reactive_with XLMOD:00037 ! non-selective
-
-[Term]
-id: XLMOD:00123
-name: thermoreactive
-def: "Indicates that a reactive group is thermoreactive." [PSI:XL]
-is_a: XLMOD:00026 ! reactive group attribute
-
-[Term]
-id: XLMOD:00124
-name: isocyanate
-def: "An isocyanate (-N=C=O) that reacts with hydroxyl groups." [PMID:21557289]
-property_value: specificities: "(S,T,Y)" xsd:string
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06500 ! secondary amine reactive
-
-[Term]
-id: XLMOD:00125
-name: hydroxyphenyl azide
-def: "A hydroxyphenyl azid photoreactive group." [PSI:XL]
-property_value: waveLengthRange: "320-350 nm" xsd:string
-is_a: XLMOD:00114 ! aryl azide
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-relationship: is_reactive_with XLMOD:00037 ! non-selective
-
-[Term]
-id: XLMOD:00126
-name: phenyl azide
-def: "A phenyl azide photoreactive group." [PSI:XL]
-synonym: "aryl nitrene" EXACT []
-property_value: waveLengthRange: "320-350 nm" xsd:string
-is_a: XLMOD:00114 ! aryl azide
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-relationship: is_reactive_with XLMOD:00037 ! non-selective
-
-[Term]
-id: XLMOD:00127
-name: iodoacetyl
-def: "A iodoacetyl reactive group, that reacts with sulfhydryl groups." [PSI:XL]
-property_value: specificities: "(C,H)" xsd:string
-is_a: XLMOD:00112 ! haloacetyl
-relationship: is_reactive_with XLMOD:00029 ! sulfhydryl reactive
-
-[Term]
-id: XLMOD:00128
-name: bromoacetyl
-def: "A bromoacetyl reactive group, that reacts with sulfhydryl groups." [PSI:XL]
-property_value: specificities: "(C,H)" xsd:string
-is_a: XLMOD:00112 ! haloacetyl
-relationship: is_reactive_with XLMOD:00029 ! sulfhydryl reactive
-
-[Term]
-id: XLMOD:00129
-name: hydroxybenzotriazole
-def: "A reactive group that reacts with amines." [PMID:19994840]
-property_value: specificities: "(K,N,Q,R,Protein N-term)" xsd:string
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:00130
-name: 1-hydroxy-7-azabenzotriazole
-def: "A reactive group that reacts with amines." [PMID:19994840]
-property_value: specificities: "(K,N,Q,R,Protein N-term)" xsd:string
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:00131
-name: thioimidate
-def: "A reactive group that reacts with amines." [PMID:20795639]
-property_value: specificities: "(K,N,Q,R,Protein N-term)" xsd:string
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:00132
-name: platinum(II)
-def: "Platinum(II) coordinates with the side chains of methionine (Met), cysteine (Cys), and histidine(His), namely, thioether, sulfhydryl, and imidazole." [PMID:21591778]
-property_value: baseSpecificities: "(Guanine)" xsd:string
-property_value: secondaryBaseSpecificities: "(Adenine, Cytosine)" xsd:string
-property_value: specificities: "(C,H,M)" xsd:string
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00029 ! sulfhydryl reactive
-relationship: is_reactive_with XLMOD:00045 ! thioether reactive
-relationship: is_reactive_with XLMOD:00046 ! imidazole reactive
-
-[Term]
-id: XLMOD:00133
-name: amine reactive group
-def: "Reactive group (-NH2) that reacts with carboxyl (-COOH) groups." [PSI:XL]
-property_value: specificities: "(D,E)" xsd:string
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-relationship: is_reactive_with XLMOD:00031 ! aldehyde reactive
-relationship: is_reactive_with XLMOD:06510 ! ketone reactive
-
-[Term]
-id: XLMOD:00134
-name: psoralen
-def: "A photoreactive group that reacts with pyrimidines, especially thymines of nucleic acids." [PSI:XL]
-property_value: specificities: "(Thy)" xsd:string
-is_a: XLMOD:00100 ! reactive group
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-relationship: is_reactive_with XLMOD:00048 ! nucleic acid reactive
-
-[Term]
-id: XLMOD:00135
-name: azido-methylcoumarin
-def: "A photoreactive azido-methylcoumarin group." [PSI:XL]
-is_a: XLMOD:00100 ! reactive group
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-relationship: is_reactive_with XLMOD:00037 ! non-selective
-
-[Term]
-id: XLMOD:00136
-name: perfluoroaryl azide
-def: "A photoreactive perfluoroaryl azide group." [PSI:XL]
-is_a: XLMOD:00114 ! aryl azide
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-relationship: is_reactive_with XLMOD:00037 ! non-selective
-
-[Term]
-id: XLMOD:00137
-name: diazo group
-def: "A photoreactive diazo (R1R2C=N=N) group." [PSI:XL]
-is_a: XLMOD:00100 ! reactive group
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-relationship: is_reactive_with XLMOD:00037 ! non-selective
-
-[Term]
-id: XLMOD:00138
-name: carboxyl
-def: "A reactive group (-COOH) that reacts with primary amine (-NH2) groups." [PSI:XL]
-property_value: specificities: "(K,N,Q,R,Protein N-term)" xsd:string
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:00139
-name: hydroxymethyl phosphine
-def: "A reactive group that reacts with amine groups." [PSI:XL]
-property_value: specificities: "(K,N,Q,R,Protein N-term)" xsd:string
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:00140
-name: vinyl sulfone
-def: "A reactive group that reacts with hydroxyl groups." [PSI:XL]
-property_value: specificities: "(C,K,N,Q,R,S,T,Y)" xsd:string
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:00029 ! sulfhydryl reactive
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-
-[Term]
-id: XLMOD:00141
-name: carbonyl
-def: "A reactive group (C=O)that reacts with hydrazines (N2H4)." [PSI:XL]
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00062 ! hydrazine reactive
-
-[Term]
-id: XLMOD:00142
-name: phenylglyoxal
-def: "An arginine-specific reactive group." [PSI:XL]
-property_value: specificities: "(R)" xsd:string
-is_a: XLMOD:00115 ! glyoxal
-
-[Term]
-id: XLMOD:00143
-name: hydrazone
-def: "A hydrazone reactive group (C=NH-NHR) that reacts with carbonyls." [PSI:XL]
-property_value: specificities: "(D,E,Protein C-term)" xsd:string
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00031 ! aldehyde reactive
-
-[Term]
-id: XLMOD:00144
-name: S-acetyl
-def: "A S-acetyl group." [PSI:XL]
-comment: Used to incorporate sulfhydryl (-SH) groups into proteins as part of a two-step or heterobifunctional crosslinking strategy.
-synonym: "SAT" EXACT []
-is_a: XLMOD:00100 ! reactive group
-
-[Term]
-id: XLMOD:00145
-name: aryl halide
-def: "An aryl halide group (Ar-halogen) that reacts with primary amines." [PSI:XL]
-property_value: specificities: "(K,N,Q,R,Protein N-term)" xsd:string
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:00037 ! non-selective
-
-[Term]
-id: XLMOD:00146
-name: dimethylether
-def: "A dimethylether (Ch3-O-CH3) reactive group that reacts with carboxyl groups." [PSI:XL]
-property_value: specificities: "(D,E)" xsd:string
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:00147
-name: photocleavable
-def: "Indicates that a reactive group is photocleavable." [PSI:XL]
-is_a: XLMOD:00108 ! photoreactive
-
-[Term]
-id: XLMOD:00148
-name: nitrobenzylester
-def: "A photocleavable group." [PSI:XL]
-is_a: XLMOD:00100 ! reactive group
-relationship: is_cleavable XLMOD:00147 ! photocleavable
-relationship: is_reactive_with XLMOD:00037 ! non-selective
-
-[Term]
-id: XLMOD:00149
-name: photoactivatable
-def: "Indicates that a reactive group is photoactivatable." [PSI:XL]
-is_a: XLMOD:00108 ! photoreactive
-
-[Term]
-id: XLMOD:00150
-name: tetrafluorophenyl ester
-def: "Tetrafluorophenyl (TFP, F4-Ph) ester." [PMID:22641729]
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:00151
-name: pentylamine
-def: "A pentylamine (CH3(CH2)4-NH2) reactive group that reacts with carboxyl groups." [PSI:XL]
-property_value: specificities: "(D,E)" xsd:string
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:00152
-name: Biotin
-def: "A biotin reactive group that reacts with avidin, streptavidin or neutravidin." [PSI:XL]
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00072 ! avidin reactive
-
-[Term]
-id: XLMOD:00153
-name: chloroethyl
-def: "A reactive group that reacts with guanin." [PSI:XL]
-is_a: XLMOD:00100 ! reactive group
-property_value: baseSpecificities: "(Guanine)" xsd:string
-property_value: secondaryBaseSpecificities: "(Adenine, Cytosine)" xsd:string
-
-[Term]
-id: XLMOD:00154
-name: imino
-def: "An imino (R1R2-C=N-R3) reactive group that reacts with primary amines." [PSI:XL]
-property_value: specificities: "(D,E,K,Protein N-term)" xsd:string
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:00155
-name: acyl chloride
-def: "An acyl chloride (R-CO-Cl) reactive group that reacts with alcohol, phenol, thiol and amines." [PMID:21557289]
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06500 ! secondary amine reactive
-relationship: is_reactive_with XLMOD:06509 ! phenol reactive
-relationship: is_reactive_with XLMOD:06513 ! thiol reactive
-
-[Term]
-id: XLMOD:00156
-name: sulfonyl chloride
-def: "A sulfonyl chloride (R-SO2-Cl) reactive group." [PMID:21557289]
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06500 ! secondary amine reactive
-relationship: is_reactive_with XLMOD:06509 ! phenol reactive
-relationship: is_reactive_with XLMOD:06513 ! thiol reactive
-
-[Term]
-id: XLMOD:00157
-name: benzofurazan
-def: "A benzofurazan (2,1,3-benzoxadiazole) reactive group." [PMID:21557289]
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-relationship: is_reactive_with XLMOD:00031 ! aldehyde reactive
-relationship: is_reactive_with XLMOD:06510 ! ketone reactive
-
-[Term]
-id: XLMOD:00158
-name: halobenzofurazan
-def: "A halobenzofurazan (2,1,3-benzoxadiazole) reactive group with a halogen (-F, -Cl) modification." [PMID:21557289]
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:00159
-name: hydrazine
-def: "A hydrazine (R-NHNH2-) reactive group." [PMID:21557289]
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-relationship: is_reactive_with XLMOD:00031 ! aldehyde reactive
-relationship: is_reactive_with XLMOD:06510 ! ketone reactive
-
-[Term]
-id: XLMOD:00160
-name: TAD
-def: "A 4-substituted 1,2,4-triazoline-3,5-dione (TAD) reactive group." [PMID:21557289]
-synonym: "1,2,4-triazoline-3,5-dione" EXACT []
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:06514 ! Vitamin D metabolite reactive
-
-[Term]
-id: XLMOD:00161
-name: boronic acid
-def: "An (alkyl- or aryl-substituted) boronic acid (R-B-(OH)2) reactive group." [PMID:21557289]
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-relationship: is_reactive_with XLMOD:06506 ! carbohydrate reactive
-
-[Term]
-id: XLMOD:00162
-name: isothiocyanate
-def: "An isothiocyanate (-N=C=S) reactive group." [PMID:21557289]
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:06500 ! secondary amine reactive
-
-[Term]
-id: XLMOD:00163
-name: chloroformate reactive group
-def: "A chloroformate (Cl-CO-OR) reactive group." [PMID:21557289]
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:06500 ! secondary amine reactive
-
-[Term]
-id: XLMOD:00164
-name: carabamate
-def: "A carbamate (O-CO-N) reactive group." [PMID:21557289]
-synonym: "urethane" EXACT []
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:06500 ! secondary amine reactive
-
-[Term]
-id: XLMOD:00165
-name: sulfonate
-def: "A sulfonate (R1-SO2O-R2) reactive group." [PMID:21557289]
-synonym: "sulphonate" EXACT []
-synonym: "sulfonic ester" EXACT []
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:00166
-name: anhydride
-def: "An anhydride (R1-CO-O-CO-R2) reactive group." [PMID:21557289]
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-
-[Term]
-id: XLMOD:00167
-name: carboxyl reactive group
-def: "Reactive group (-COOH) that reacts with amino (-NH2) groups." [PSI:XL]
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00028 ! amine reactive
-
-[Term]
-id: XLMOD:00168
-name: benzyl bromide reactive group
-def: "A benzyl bromide (C6H5CH2Br) reactive group." [PMID:21557289]
-synonym: "Bn-Br" EXACT []
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00029 ! sulfhydryl reactive
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-relationship: is_reactive_with XLMOD:06509 ! phenol reactive
-relationship: is_reactive_with XLMOD:06521 ! phosphate reactive
-
-[Term]
-id: XLMOD:00169
-name: sodium dithionite cleavable
-def: "Indicates that a cross-linker is chemically cleavable by sodium dithionite." [PSI:XL]
-is_a: XLMOD:00017 ! chemically cleavable
-
-[Term]
-id: XLMOD:00170
-name: benzoyl bromide
-def: "A benzoyl bromide (C6H5COBr) reactive group." [PMID:21557289]
-synonym: "Bz-Br" EXACT []
-is_a: XLMOD:00100 ! reactive group
-relationship: is_reactive_with XLMOD:00029 ! sulfhydryl reactive
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-relationship: is_reactive_with XLMOD:06509 ! phenol reactive
-relationship: is_reactive_with XLMOD:06521 ! phosphate reactive
-
-[Term]
-id: XLMOD:00171
-name: Ortho-phthalaldehyde
-def: "A lysine-specific reactive group." [PSI:XL]
-synonym: "OPA" EXACT []
-property_value: specificities: "(K)" xsd:string
-is_a: XLMOD:00116 ! aldehyde
-
-[Term]
-id: XLMOD:00172
-name: IMAC-enrichable
-def: "Indicates a cross-linker facilitating IMAC (immobilized metal affinity chromatography) enrichment." [PSI:XL]
-is_a: XLMOD:00019 ! enrichable
-
-[Term]
-id: XLMOD:00173
-name: phosphonic acid
-def: "A phosphonic acid handle, which can be used for IMAC-enrichment." [PSI:XL]
-is_a: XLMOD:00050 ! handle
-is_a: XLMOD:00172 ! IMAC-enrichable
-
-[Term]
-id: XLMOD:01000
-name: hydrolyzed BS3
-def: "Hydrolyzed bis(sulfosuccinimidyl)suberate." [PSI:XL]
-property_value: deadEndFormula: "C8 H12 O3" xsd:string
-property_value: monoIsotopicMass: "156.07864431" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02000 ! BS3
-
-[Term]
-id: XLMOD:01001
-name: ammonium amidated BS3
-def: "Ammonium amidated bis(sulfosuccinimidyl)suberate." [PSI:XL]
-property_value: deadEndFormula: "C8 H13 O2 N" xsd:string
-property_value: monoIsotopicMass: "155.094628715" xsd:double
-is_a: XLMOD:00095 ! ammonium amidation cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00021 ! ammonium amidated
-relationship: is_side_product_of XLMOD:02000 ! BS3
-
-[Term]
-id: XLMOD:01002
-name: hydrolyzed DSS
-def: "Hydrolyzed disuccinimidyl suberate." [PSI:XL]
-property_value: deadEndFormula: "C8 H12 O3" xsd:string
-property_value: monoIsotopicMass: "156.07864431" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02001 ! DSS
-
-[Term]
-id: XLMOD:01003
-name: ammonium amidated DSS
-def: "Ammonium amidated disuccinimidyl suberate." [PSI:XL]
-property_value: deadEndFormula: "C8 H13 O2 N" xsd:string
-property_value: monoIsotopicMass: "155.094628715" xsd:double
-is_a: XLMOD:00095 ! ammonium amidation cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00021 ! ammonium amidated
-relationship: is_side_product_of XLMOD:02001 ! DSS
-
-[Term]
-id: XLMOD:01004
-name: hydrolyzed DSS-d4
-def: "Deuterium labelled hydrolyzed disuccinimidyl 2,2,7,7-suberate." [PSI:XL]
-property_value: monoIsotopicMass: "160.1037416836" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02002 ! DSS-d4
-
-[Term]
-id: XLMOD:01005
-name: ammonium amidated DSS-d4
-def: "Deuterium labelled ammonium amidated disuccinimidyl 2,2,7,7-suberate." [PSI:XL]
-property_value: monoIsotopicMass: "159.1197260886" xsd:double
-is_a: XLMOD:00095 ! ammonium amidation cross-linker related chemical modification
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_partially_reacted XLMOD:00021 ! ammonium amidated
-relationship: is_side_product_of XLMOD:02002 ! DSS-d4
-
-[Term]
-id: XLMOD:01006
-name: hydrolyzed DSS-d12
-def: "Deuterium labelled hydrolyzed disuccinimidyl 2,2,3,3,4,4,5,5,6,6,7,7-suberate." [PSI:XL]
-property_value: monoIsotopicMass: "168.153965238" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02003 ! DSS-d12
-
-[Term]
-id: XLMOD:01007
-name: ammonium amidated DSS-d12
-def: "Deuterium labelled ammonium amidated disuccinimidyl 2,2,3,3,4,4,5,5,6,6,7,7-suberate." [PSI:XL]
-property_value: monoIsotopicMass: "167.169949643" xsd:double
-is_a: XLMOD:00095 ! ammonium amidation cross-linker related chemical modification
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_partially_reacted XLMOD:00021 ! ammonium amidated
-relationship: is_side_product_of XLMOD:02003 ! DSS-d12
-
-[Term]
-id: XLMOD:01008
-name: hydrolyzed BS3-d4
-def: "Deuterium labelled hydrolyzed bis(sulfosuccinimidyl) 2,2,7,7-suberate." [PSI:XL]
-property_value: deadEndFormula: "C8 D4 H8 O3" xsd:string
-property_value: monoIsotopicMass: "160.103751286" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02004 ! BS3-d4
-
-[Term]
-id: XLMOD:01009
-name: ammonium amidated BS3-d4
-def: "Deuterium labelled ammonium amidated bis(sulfosuccinimidyl) 2,2,7,7-suberate." [PSI:XL]
-property_value: deadEndFormula: "C8 D4 H9 N1 O2" xsd:string
-property_value: monoIsotopicMass: "159.119735691" xsd:double
-is_a: XLMOD:00095 ! ammonium amidation cross-linker related chemical modification
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_partially_reacted XLMOD:00021 ! ammonium amidated
-relationship: is_side_product_of XLMOD:02004 ! BS3-d4
-
-[Term]
-id: XLMOD:01010
-name: hydrolyzed BS2G
-def: "Hydrolyzed bis(sulfosuccinimidyl) glutarate." [PSI:XL]
-property_value: deadEndFormula: "C5 H6 O3" xsd:string
-property_value: monoIsotopicMass: "114.0316941" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02005 ! BS2G
-
-[Term]
-id: XLMOD:01011
-name: ammonium amidated BS2G
-def: "Ammonium amidated bis(sulfosuccinimidyl) glutarate." [PSI:XL]
-property_value: deadEndFormula: "C5 H7 N1 O2" xsd:string
-property_value: monoIsotopicMass: "113.047678505" xsd:double
-is_a: XLMOD:00095 ! ammonium amidation cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00021 ! ammonium amidated
-relationship: is_side_product_of XLMOD:02005 ! BS2G
-
-[Term]
-id: XLMOD:01012
-name: hydrolyzed DSG
-def: "Hydrolyzed disuccinimidyl glutarate." [PSI:XL]
-property_value: deadEndFormula: "C5 H6 O3" xsd:string
-property_value: monoIsotopicMass: "114.0316941" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02006 ! DSG
-
-[Term]
-id: XLMOD:01013
-name: ammonium amidated DSG
-def: "Ammonium amidated disuccinimidyl glutarate." [PSI:XL]
-property_value: deadEndFormula: "C5 H7 N1 O2" xsd:string
-property_value: monoIsotopicMass: "113.047678505" xsd:double
-is_a: XLMOD:00095 ! ammonium amidation cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00021 ! ammonium amidated
-relationship: is_side_product_of XLMOD:02006 ! DSG
-
-[Term]
-id: XLMOD:01014
-name: hydrolyzed DSG-d4
-def: "Deuterium labelled hydrolyzed disuccinimidyl 2,2,4,4-glutarate." [PSI:XL]
-property_value: deadEndFormula: "C5 D4 H2 O3" xsd:string
-property_value: monoIsotopicMass: "118.0567741" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02007 ! DSG-d4
-
-[Term]
-id: XLMOD:01015
-name: ammonium amidated DSG-d4
-def: "Deuterium labelled ammonium amidated disuccinimidyl 2,2,4,4-glutarate." [PSI:XL]
-property_value: deadEndFormula: "C5 D4 H3 N1 O2" xsd:string
-property_value: monoIsotopicMass: "117.072758505" xsd:double
-is_a: XLMOD:00095 ! ammonium amidation cross-linker related chemical modification
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_partially_reacted XLMOD:00021 ! ammonium amidated
-relationship: is_side_product_of XLMOD:02007 ! DSG-d4
-
-[Term]
-id: XLMOD:01016
-name: hydrolyzed BS2G-d4
-def: "Deuterium labelled hydrolyzed bis(sulfosuccinimidyl) 2,2,4,4-glutarate." [PSI:XL]
-property_value: deadEndFormula: "C5 D4 H2 O3" xsd:string
-property_value: monoIsotopicMass: "118.056801076" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02008 ! BS2G-d4
-
-[Term]
-id: XLMOD:01017
-name: ammonium amidated BS2G-d4
-def: "Deuterium labelled ammonium amidated bis(sulfosuccinimidyl) 2,2,4,4-glutarate." [PSI:XL]
-property_value: deadEndFormula: "C5 D4 H3 N1 O2" xsd:string
-property_value: monoIsotopicMass: "117.072785481" xsd:double
-is_a: XLMOD:00095 ! ammonium amidation cross-linker related chemical modification
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_partially_reacted XLMOD:00021 ! ammonium amidated
-relationship: is_side_product_of XLMOD:02008 ! BS2G-d4
-
-[Term]
-id: XLMOD:01018
-name: BDP-NHP-stump
-def: "Biotin Aspartate Proline n-hydroxyphthalimide-stump." [PMID:23413883, PMID:26235782, PMID:27089058]
-property_value: monoIsotopicMass: "197.032422395" xsd:double
-is_a: XLMOD:00002 ! cross-linker related chemical modification
-relationship: is_side_product_of XLMOD:02011 ! BDP-NHP
-
-[Term]
-id: XLMOD:01019
-name: hydrolyzed DSP
-def: "Hydrolyzed dithiobis[succinimidyl propionate." [PSI:XL]
-property_value: deadEndFormula: "C6 H8 O3 S2" xsd:string
-property_value: monoIsotopicMass: "191.99148557" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02029 ! DSP
-
-[Term]
-id: XLMOD:01020
-name: ammonium amidated DSP
-def: "Ammonium amidated dithiobis[succinimidyl propionate." [PSI:XL]
-property_value: deadEndFormula: "C6 H9 N1 O2 S2" xsd:string
-property_value: monoIsotopicMass: "191.007469975" xsd:double
-is_a: XLMOD:00095 ! ammonium amidation cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00021 ! ammonium amidated
-relationship: is_side_product_of XLMOD:02029 ! DSP
-
-[Term]
-id: XLMOD:01021
-name: hydrolyzed EGS
-def: "Hydrolyzed ethylene glycolbis(succinimidylsuccinate)." [PSI:XL]
-property_value: deadEndFormula: "C10 H12 O7" xsd:string
-property_value: monoIsotopicMass: "244.0583027" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02034 ! EGS
-
-[Term]
-id: XLMOD:01022
-name: ammonium amidated EGS
-def: "Ammonium amidated ethylene glycolbis(succinimidylsuccinate)." [PSI:XL]
-property_value: deadEndFormula: "C10 H13 N1 O6" xsd:string
-property_value: monoIsotopicMass: "243.074287105" xsd:double
-is_a: XLMOD:00095 ! ammonium amidation cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00021 ! ammonium amidated
-relationship: is_side_product_of XLMOD:02034 ! EGS
-
-[Term]
-id: XLMOD:01023
-name: hydrolyzed BiPS
-def: "Hydrolyzed bimane bisthiopropionic acid N-succinimidyl ester." [PMID:18838738]
-property_value: deadEndFormula: "C16 H18 N2 O5 S2" xsd:string
-property_value: monoIsotopicMass: "382.06571" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02040 ! BiPS
-
-[Term]
-id: XLMOD:01024
-name: ammonium amidated BiPS
-def: "Ammonium amidated bimane bisthiopropionic acid N-succinimidyl ester." [PMID:18838738]
-property_value: deadEndFormula: "C16 H18 N3 O4 S2" xsd:string
-property_value: monoIsotopicMass: "381.08169" xsd:double
-is_a: XLMOD:00095 ! ammonium amidation cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00021 ! ammonium amidated
-relationship: is_side_product_of XLMOD:02040 ! BiPS
-
-[Term]
-id: XLMOD:01025
-name: hydrolyzed CBDPS
-def: "Hydrolyzed cyanurbiotindipropionylsuccinimide." [PMID:20622150]
-property_value: deadEndFormula: "C19 H25 N7 O5 S3" xsd:string
-property_value: monoIsotopicMass: "527.10738" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02041 ! CBDPS
-
-[Term]
-id: XLMOD:01026
-name: ammonium amidated CBDPS
-def: "Ammonium amidated cyanurbiotindipropionylsuccinimide." [PMID:20622150]
-property_value: deadEndFormula: "C19 H25 N8 O4 S3" xsd:string
-property_value: monoIsotopicMass: "526.12336" xsd:double
-is_a: XLMOD:00095 ! ammonium amidation cross-linker related chemical modification
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: is_partially_reacted XLMOD:00021 ! ammonium amidated
-relationship: is_side_product_of XLMOD:02041 ! CBDPS
-
-[Term]
-id: XLMOD:01027
-name: hydrolyzed DSA
-def: "Hydrolyzed disuccinimidyladipic acid." [PSI:XL]
-property_value: deadEndFormula: "C6 H8 O3" xsd:string
-property_value: monoIsotopicMass: "128.04680" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02044 ! DSA
-
-[Term]
-id: XLMOD:01028
-name: ammonium amidated DSA
-def: "Ammonium amidated disuccinimidyladipic acid." [PSI:XL]
-property_value: deadEndFormula: "C6 H9 N1 O2" xsd:string
-property_value: monoIsotopicMass: "127.06278" xsd:double
-is_a: XLMOD:00095 ! ammonium amidation cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00021 ! ammonium amidated
-relationship: is_side_product_of XLMOD:02044 ! DSA
-
-[Term]
-id: XLMOD:01029
-name: hydrolyzed DNBDPS
-def: "Hydrolyzed DNBDPS." [PMID:20109223]
-property_value: deadEndFormula: "C12 H10 N2 O7 S2" xsd:string
-property_value: monoIsotopicMass: "357.99294" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: has_handle XLMOD:00054 ! DNB
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02045 ! DNBDPS
-
-[Term]
-id: XLMOD:01030
-name: ammonium amidated DNBDPS
-def: "Ammonium amidated DNBDPS." [PMID:20109223]
-property_value: deadEndFormula: "C12 H10 N3 O6 S2" xsd:string
-property_value: monoIsotopicMass: "357.00892" xsd:double
-is_a: XLMOD:00095 ! ammonium amidation cross-linker related chemical modification
-relationship: has_handle XLMOD:00054 ! DNB
-relationship: is_partially_reacted XLMOD:00021 ! ammonium amidated
-relationship: is_side_product_of XLMOD:02045 ! DNBDPS
-
-[Term]
-id: XLMOD:01031
-name: hydrolyzed TEABS
-def: "Hydrolyzed TEABS cross-linking reagent." [PMID:20109223]
-property_value: deadEndFormula: "C28 H41 N5 O12 S1" xsd:string
-property_value: monoIsotopicMass: "671.24724" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02046 ! TEABS
-
-[Term]
-id: XLMOD:01032
-name: ammonium amidated TEABS
-def: "Ammonium amidated TEABS cross-linking reagent." [PMID:20109223]
-property_value: deadEndFormula: "C28 H41 N6 O11 S1" xsd:string
-property_value: monoIsotopicMass: "670.26322" xsd:double
-is_a: XLMOD:00095 ! ammonium amidation cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00021 ! ammonium amidated
-relationship: is_side_product_of XLMOD:02046 ! TEABS
-
-[Term]
-id: XLMOD:01033
-name: hydrolyzed DTSSP-d8
-def: "Hydrolyzed deuterium labelled 3,3'-Dithiobis[sulfosuccinimidylpropionate]." [PMID:10975572, PMID:18510349]
-property_value: deadEndFormula: "C6 D8 O3 S2" xsd:string
-property_value: monoIsotopicMass: "191.99149" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02049 ! DTSSP
-
-[Term]
-id: XLMOD:01034
-name: ammonium amidated DTSSP-d8
-def: "Ammonium amidated deuterium labelled 3,3'-Dithiobis[sulfosuccinimidylpropionate]." [PMID:10975572, PMID:18510349]
-property_value: deadEndFormula: "C6 D8 H1 N1 O2 S2" xsd:string
-property_value: monoIsotopicMass: "191.00747" xsd:double
-is_a: XLMOD:00095 ! ammonium amidation cross-linker related chemical modification
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_partially_reacted XLMOD:00021 ! ammonium amidated
-relationship: is_side_product_of XLMOD:02049 ! DTSSP
-
-[Term]
-id: XLMOD:01035
-name: hydrolyzed DSP-d8
-def: "Hydrolyzed deuterium-labelled dithiobis[succinimidyl propionate." [PSI:XL]
-property_value: deadEndFormula: "C6 D8 O3 S2" xsd:string
-property_value: monoIsotopicMass: "200.04165" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02030 ! DSP-d8
-
-[Term]
-id: XLMOD:01036
-name: ammonium amidated DSP-d8
-def: "Ammonium amidated deuterium-labelled dithiobis[succinimidyl propionate." [PSI:XL]
-property_value: deadEndFormula: "C6 D8 H1 N1 O2 S2" xsd:string
-property_value: monoIsotopicMass: "199.05763" xsd:double
-is_a: XLMOD:00095 ! ammonium amidation cross-linker related chemical modification
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_partially_reacted XLMOD:00021 ! ammonium amidated
-relationship: is_side_product_of XLMOD:02030 ! DSP-d8
-
-[Term]
-id: XLMOD:01037
-name: hydrolyzed Sulfo-EGS
-def: "Hydrolyzed ethylene glycolbis(sulfosuccinimidylsuccinate)." [PSI:XL]
-property_value: deadEndFormula: "C10 H12 O7" xsd:string
-property_value: monoIsotopicMass: "244.0583028" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02035 ! Sulfo-EGS
-
-[Term]
-id: XLMOD:01038
-name: ammonium amidated Sulfo-EGS
-def: "Ammonium amidated ethylene glycolbis(sulfosuccinimidylsuccinate)." [PSI:XL]
-property_value: deadEndFormula: "C10 H12 N1 O6" xsd:string
-property_value: monoIsotopicMass: "243.07428" xsd:double
-is_a: XLMOD:00095 ! ammonium amidation cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00021 ! ammonium amidated
-relationship: is_side_product_of XLMOD:02035 ! Sulfo-EGS
-
-[Term]
-id: XLMOD:01039
-name: hydrolyzed EGS-d12
-def: "Deuterium labelled hydrolyzed ethylene glycolbis(succinimidylsuccinate)." [PSI:XL]
-property_value: deadEndFormula: "C10 D12 O7" xsd:string
-property_value: monoIsotopicMass: "256.13403" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02050 ! EGS-d12
-
-[Term]
-id: XLMOD:01040
-name: ammonium amidated EGS-d12
-def: "Deuterium labelled ammonium amidated ethylene glycolbis(succinimidylsuccinate)." [PSI:XL]
-property_value: deadEndFormula: "C10 D12 N1 O6" xsd:string
-property_value: monoIsotopicMass: "255.15001" xsd:double
-is_a: XLMOD:00095 ! ammonium amidation cross-linker related chemical modification
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_partially_reacted XLMOD:00021 ! ammonium amidated
-relationship: is_side_product_of XLMOD:02050 ! EGS-d12
-
-[Term]
-id: XLMOD:01041
-name: hydrolyzed Sulfo-EGS-d12
-def: "Deuterium labelled hydrolyzed ethylene glycolbis(sulfosuccinimidylsuccinate)." [PSI:XL]
-property_value: deadEndFormula: "C10 D12 O7" xsd:string
-property_value: monoIsotopicMass: "256.13403" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02050 ! Sulfo-EGS-d12
-
-[Term]
-id: XLMOD:01042
-name: ammonium amidated Sulfo-EGS-d12
-def: "Deuterium labelled ammonium amidated ethylene glycolbis(sulfosuccinimidylsuccinate)." [PSI:XL]
-property_value: deadEndFormula: "C10 D12 N1 O6" xsd:string
-property_value: monoIsotopicMass: "255.15001" xsd:double
-is_a: XLMOD:00095 ! ammonium amidation cross-linker related chemical modification
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_partially_reacted XLMOD:00021 ! ammonium amidated
-relationship: is_side_product_of XLMOD:02050 ! Sulfo-EGS-d12
-
-[Term]
-id: XLMOD:01043
-name: hydrolyzed DSA-13C6
-def: "Hydrolyzed 13C labelled disuccinimidyladipic acid." [PSI:XL]
-property_value: deadEndFormula: "13C6 H8 O3" xsd:string
-property_value: monoIsotopicMass: "134.06696" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_labelled XLMOD:00036 ! 13C labelled
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02054 ! DSA-13C6
-
-[Term]
-id: XLMOD:01044
-name: ammonium amidated DSA-13C6
-def: "Ammonium amidated 13C labelled disuccinimidyladipic acid." [PSI:XL]
-property_value: deadEndFormula: "13C6 H9 N1 O2" xsd:string
-property_value: monoIsotopicMass: "133.08294" xsd:double
-is_a: XLMOD:00095 ! ammonium amidation cross-linker related chemical modification
-relationship: is_labelled XLMOD:00036 ! 13C labelled
-relationship: is_partially_reacted XLMOD:00021 ! ammonium amidated
-relationship: is_side_product_of XLMOD:02054 ! DSA-13C6
-
-[Term]
-id: XLMOD:01045
-name: hydrolyzed CBDPS-d8
-def: "Deuterium labelled hydrolyzed cyanurbiotindipropionylsuccinimide." [PMID:20622150]
-property_value: deadEndFormula: "C19 D8 H17 N7 O5 S3" xsd:string
-property_value: monoIsotopicMass: "535.15754" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02055 ! CBDPS-d8
-
-[Term]
-id: XLMOD:01046
-name: ammonium amidated CBDPS-d8
-def: "Deuterium labelled ammonium amidated cyanurbiotindipropionylsuccinimide." [PMID:20622150]
-property_value: deadEndFormula: "C19 D8 H17 N8 O4 S3" xsd:string
-property_value: monoIsotopicMass: "534.17352" xsd:double
-is_a: XLMOD:00095 ! ammonium amidation cross-linker related chemical modification
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_partially_reacted XLMOD:00021 ! ammonium amidated
-relationship: is_side_product_of XLMOD:02055 ! CBDPS-d8
-
-[Term]
-id: XLMOD:01047
-name: hydrolyzed CBDPSS
-def: "Hydrolyzed cyanurbiotindimercaptopropionylsulfosuccinimide." [PMID:20622150]
-property_value: deadEndFormula: "C19 H25 N7 O5 S3" xsd:string
-property_value: monoIsotopicMass: "527.10738" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02056 ! CBDPSS
-
-[Term]
-id: XLMOD:01048
-name: ammonium amidated CBDPSS
-def: "Ammonium amidated cyanurbiotindimercaptopropionylsulfosuccinimide." [PMID:20622150]
-property_value: deadEndFormula: "C19 H25 N8 O4 S3" xsd:string
-property_value: monoIsotopicMass: "526.12336" xsd:double
-is_a: XLMOD:00095 ! ammonium amidation cross-linker related chemical modification
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: is_partially_reacted XLMOD:00021 ! ammonium amidated
-relationship: is_side_product_of XLMOD:02056 ! CBDPSS
-
-[Term]
-id: XLMOD:01049
-name: hydrolyzed CBDPSS-d8
-def: "Deuterium labelled hydrolyzed cyanurbiotindimercaptopropionylsulfosuccinimide." [PMID:20622150]
-property_value: deadEndFormula: "C19 D8 H17 N7 O5 S3" xsd:string
-property_value: monoIsotopicMass: "535.15754" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02057 ! CBDPSS-d8
-
-[Term]
-id: XLMOD:01050
-name: ammonium amidated CBDPSS-d8
-def: "Deuterium labelled ammonium amidated cyanurbiotindimercaptopropionylsulfosuccinimide." [PMID:20622150]
-property_value: deadEndFormula: "C19 D8 H17 N8 O4 S3" xsd:string
-property_value: monoIsotopicMass: "534.17352" xsd:double
-is_a: XLMOD:00095 ! ammonium amidation cross-linker related chemical modification
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_partially_reacted XLMOD:00021 ! ammonium amidated
-relationship: is_side_product_of XLMOD:02057 ! CBDPSS-d8
-
-[Term]
-id: XLMOD:01051
-name: hydrolyzed BS3-d12
-def: "Deuterium labelled hydrolyzed bis(sulfosuccinimidyl) 2,2,3,3,4,4,5,5,6,6,7,7-suberate." [PSI:XL]
-property_value: deadEndFormula: "C8 D12 O3" xsd:string
-property_value: monoIsotopicMass: "168.15437" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02064 ! BS3-d12
-
-[Term]
-id: XLMOD:01052
-name: ammonium amidated BS3-d12
-def: "Deuterium labelled ammonium amidated bis(sulfosuccinimidyl) 2,2,3,3,4,4,5,5,6,6,7,7-suberate." [PSI:XL]
-property_value: deadEndFormula: "C8 D12 H1 N1 O2" xsd:string
-property_value: monoIsotopicMass: "167.17035" xsd:double
-is_a: XLMOD:00095 ! ammonium amidation cross-linker related chemical modification
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_partially_reacted XLMOD:00021 ! ammonium amidated
-relationship: is_side_product_of XLMOD:02064 ! BS3-d12
-
-[Term]
-id: XLMOD:01053
-name: hydrolyzed DSG-d6
-def: "Deuterium labelled hydrolyzed disuccinimidyl 2,2,3,3,4,4-glutarate." [PSI:XL]
-property_value: deadEndFormula: "C5 D6 O3" xsd:string
-property_value: monoIsotopicMass: "120.07483" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02065 ! DSG-d6
-
-[Term]
-id: XLMOD:01054
-name: ammonium amidated DSG-d6
-def: "Deuterium labelled ammonium amidated disuccinimidyl 2,2,3,3,4,4-glutarate." [PSI:XL]
-property_value: deadEndFormula: "C5 D6 H1 N1 O2" xsd:string
-property_value: monoIsotopicMass: "119.09081" xsd:double
-is_a: XLMOD:00095 ! ammonium amidation cross-linker related chemical modification
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_partially_reacted XLMOD:00021 ! ammonium amidated
-relationship: is_side_product_of XLMOD:02065 ! DSG-d6
-
-[Term]
-id: XLMOD:01055
-name: hydrolyzed BS2G-d6
-def: "Deuterium labelled hydrolyzed bis(sulfosuccinimidyl) 2,2,3,3,4,4-glutarate." [PSI:XL]
-property_value: deadEndFormula: "C5 D6 O3" xsd:string
-property_value: monoIsotopicMass: "120.06877" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02066 ! BS2G-d6
-
-[Term]
-id: XLMOD:01056
-name: ammonium amidated BS2G-d6
-def: "Deuterium labelled ammonium amidated bis(sulfosuccinimidyl) 2,2,3,3,4,4-glutarate." [PSI:XL]
-property_value: deadEndFormula: "C5 D6 H1 N1 O2" xsd:string
-property_value: monoIsotopicMass: "119.08475" xsd:double
-is_a: XLMOD:00095 ! ammonium amidation cross-linker related chemical modification
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_partially_reacted XLMOD:00021 ! ammonium amidated
-relationship: is_side_product_of XLMOD:02066 ! BS2G-d6
-
-[Term]
-id: XLMOD:01057
-name: hydrolyzed SDH
-def: "Hydrolyzed Suberic acid 1,8-dihydrazide." [PMID:24938783]
-property_value: deadEndFormula: "C8 H16 N4 O1" xsd:string
-property_value: monoIsotopicMass: "184.13241119" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02058 ! SDH
-
-[Term]
-id: XLMOD:01058
-name: hydrolyzed SDH-d12
-def: "Deuterium labelled hydrolyzed suberic acid 1,8-dihydrazide." [PMID:24938783]
-property_value: deadEndFormula: "C8 D12 H4 N4 O1" xsd:string
-property_value: monoIsotopicMass: "196.207732118" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02059 ! SDH-d12
-
-[Term]
-id: XLMOD:01059
-name: hydrolyzed ADH
-def: "Hydrolyzed adipic acid 1,6-dihydrazide." [PMID:24938783]
-property_value: deadEndFormula: "C6 H12 N4 O1" xsd:string
-property_value: monoIsotopicMass: "156.10111105" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02060 ! ADH
-
-[Term]
-id: XLMOD:01060
-name: hydrolyzed ADH-d8
-def: "Deuterium labelled hydrolyzed adipic acid 1,6-dihydrazide." [PMID:24938783]
-property_value: deadEndFormula: "C6 D8 H4 N4 O1" xsd:string
-property_value: monoIsotopicMass: "164.151325002" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02060 ! ADH-d8
-
-[Term]
-id: XLMOD:01061
-name: hydrolyzed GDH
-def: "Hydrolyzed glutaric acid 1,5-dihydrazide." [PMID:24938783]
-property_value: deadEndFormula: "C5 H10 N4 O1" xsd:string
-property_value: monoIsotopicMass: "142.08546098" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02062 ! GDH
-
-[Term]
-id: XLMOD:01062
-name: hydrolyzed GDH-d6
-def: "Deuterium labelled hydrolyzed glutaric acid 1,5-dihydrazide." [PMID:24938783]
-property_value: deadEndFormula: "C5 D6 H4 N4 O1" xsd:string
-property_value: monoIsotopicMass: "148.123121444" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02063 ! GDH-d6
-
-[Term]
-id: XLMOD:01063
-name: hydrolyzed BCCL1
-def: "Hydrolyzed bis-(N-hydroxysuccinimidyl) 3-amino-N-biotinoyl-1,5-pentanedioate." [PMID:19412923]
-property_value: monoIsotopicMass: "355.12019" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02108 ! BCCL1
-
-[Term]
-id: XLMOD:01064
-name: hydrolyzed BCCL2
-def: "Hydrolyzed bis-(N-hydroxysuccinimidyl) 5-amino-N-biotinoyl-1,9-nonanedioate." [PMID:19412923]
-property_value: monoIsotopicMass: "411.18179" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02109 ! BCCL2
-
-[Term]
-id: XLMOD:01065
-name: hydrolyzed IRCX
-def: "Hydrolyzed dibenzoyloxysuccinimidylethyl phosphate." [PMID:18517224]
-property_value: monoIsotopicMass: "348.0" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02116 ! ICRX
-
-[Term]
-id: XLMOD:01066
-name: hydrolyzed azide-DSG
-def: "Hydrolyzed bis(succinimidyl)-3-azidomethyl glutarate." [PMID:20472459]
-property_value: monoIsotopicMass: "229.0" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02118 ! azide-DSG
-
-[Term]
-id: XLMOD:01067
-name: hydrolyzed JMV 3378
-def: "Hydrolyzed crosslinking reagent JMV 3378." [PMID:19902427]
-property_value: monoIsotopicMass: "286.0" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02120 ! JMV 3378
-
-[Term]
-id: XLMOD:01068
-name: hydrolyzed BuTuGPG
-def: "Hydrolyzed 4-[3-(2-{2-[(2,5-dioxo-pyrrolidin-1-yloxycarbonyl-methyl)-carbamoyl]-pyrrolidin-1-yl}-2-oxo-ethyl)-thioureido]-butyric acid 2,5-dioxo-pyrrolidin-1-yl ester." [PMID:19950134]
-property_value: monoIsotopicMass: "1704.86" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02121 ! BuTuGPG
-
-[Term]
-id: XLMOD:01069
-name: hydrolyzed BuUrBu
-def: "Hydrolyzed NHS-amino butyric acid-urea-amino butyric acid-NHS." [PMID:21157862]
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02122 ! BuUrBu
-
-[Term]
-id: XLMOD:01070
-name: hydrolyzed DEST
-def: "Hydrolyzed diethylsuberthioimidate." [PMID:20795639, PMID:22460622]
-property_value: deadEndFormula: "C8 H14 N2 O1" xsd:string
-property_value: monoIsotopicMass: "154.11061312" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02129 ! DEST
-
-[Term]
-id: XLMOD:01071
-name: ammonium amidated DEST
-def: "Ammonium amidated diethylsuberthioimidate." [PMID:20795639, PMID:22460622]
-property_value: deadEndFormula: "C8 H15 N3" xsd:string
-property_value: monoIsotopicMass: "153.126593" xsd:double
-is_a: XLMOD:00095 ! ammonium amidation cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00021 ! ammonium amidated
-relationship: is_side_product_of XLMOD:02129 ! DEST
-
-[Term]
-id: XLMOD:01072
-name: thioesterized DEST
-def: "Thioesterized diethylsuberthioimidate." [PMID:20795639, PMID:22460622]
-property_value: deadEndFormula: "C10 H17 N1 O1 S1" xsd:string
-property_value: monoIsotopicMass: "199.103084925" xsd:double
-is_a: XLMOD:00098 ! thioesterization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00047 ! thioesterized
-relationship: is_side_product_of XLMOD:02129 ! DEST
-
-[Term]
-id: XLMOD:01073
-name: hydrolyzed BS(PEG)5
-def: "Hydrolyzed bis(sulfosuccinimidyl)suberate pentaethyleneglycol." [PSI:XL]
-property_value: deadEndFormula: "C14 H24 O8" xsd:string
-property_value: monoIsotopicMass: "320.1471147" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02198 ! BS(PEG)5
-
-[Term]
-id: XLMOD:01074
-name: ammonium amidated BS(PEG)5
-def: "Ammonium amidated bis(sulfosuccinimidyl)suberate pentaethyleneglycol." [PSI:XL]
-property_value: deadEndFormula: "C14 H27 N1 O7" xsd:string
-property_value: monoIsotopicMass: "320.1471147" xsd:double
-is_a: XLMOD:00095 ! ammonium amidation cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00021 ! ammonium amidated
-relationship: is_side_product_of XLMOD:02198 ! BS(PEG)5
-
-[Term]
-id: XLMOD:01075
-name: hydrolyzed BSOCOES
-def: "Hydrolyzed bis(2-[Succinimidooxycarbonyloxy]ethyl) sulfone." [PSI:XL]
-property_value: deadEndFormula: "C6 H8 O7 S1" xsd:string
-property_value: monoIsotopicMass: "223.9990767" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02079 ! BSOCOES
-
-[Term]
-id: XLMOD:01076
-name: ammonium amidated BSOCOES
-def: "Ammonium amidated bis(2-[Succinimidooxycarbonyloxy]ethyl) sulfone." [PSI:XL]
-property_value: deadEndFormula: "C6 H9 N1 O6 S1" xsd:string
-property_value: monoIsotopicMass: "223.015061105" xsd:double
-is_a: XLMOD:00095 ! ammonium amidation cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00021 ! ammonium amidated
-relationship: is_side_product_of XLMOD:02079 ! BSOCOES
-
-[Term]
-id: XLMOD:01077
-name: hydrolyzed DST
-def: "Hydrolyzed disuccinimidyl tartrate." [PSI:XL]
-property_value: deadEndFormula: "C4 H4 O5" xsd:string
-property_value: monoIsotopicMass: "132.0058747" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02032 ! DST
-
-[Term]
-id: XLMOD:01078
-name: ammonium amidated DST
-def: "Ammonium amidated disuccinimidyl tartrate." [PSI:XL]
-property_value: deadEndFormula: "C4 H5 N1 O4" xsd:string
-property_value: monoIsotopicMass: "131.021859105" xsd:double
-is_a: XLMOD:00095 ! ammonium amidation cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00021 ! ammonium amidated
-relationship: is_side_product_of XLMOD:02032 ! DST
-
-[Term]
-id: XLMOD:01079
-name: hydrolyzed SDA
-def: "Hydrolyzed succinimidyl-ester diazirine." [PSI:XL]
-property_value: deadEndFormula: "C5 H8 O2" xsd:string
-property_value: monoIsotopicMass: "100.05242954" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02138 ! SDA
-
-[Term]
-id: XLMOD:01080
-name: oxidized SDA
-def: "Oxidized succinimidyl-ester diazirine." [PSI:XL]
-property_value: deadEndFormula: "C5 H6 O2" xsd:string
-property_value: monoIsotopicMass: "98.03677947" xsd:double
-is_a: XLMOD:00097 ! oxidation cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00064 ! oxidized
-relationship: is_side_product_of XLMOD:02138 ! SDA
-
-[Term]
-id: XLMOD:01081
-name: alkenized SDA
-def: "Alkenized succinimidyl-ester diazirine." [PSI:XL]
-property_value: deadEndFormula: "C4 H4 O1" xsd:string
-property_value: monoIsotopicMass: "68.02621477" xsd:double
-is_a: XLMOD:00094 ! alkenization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00065 ! alkenized
-relationship: is_side_product_of XLMOD:02138 ! SDA
-
-[Term]
-id: XLMOD:01082
-name: hydrolyzed LC-SDA
-def: "Hydrolyzed LC-SDA." [PSI:XL]
-property_value: deadEndFormula: "C11 H19 N1 O3" xsd:string
-property_value: monoIsotopicMass: "213.136493555" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02139 ! LC-SDA
-
-[Term]
-id: XLMOD:01083
-name: oxidized LC-SDA
-def: "Oxidized LC-SDA." [PSI:XL]
-property_value: deadEndFormula: "C11 H17 N1 O3" xsd:string
-property_value: monoIsotopicMass: "211.120843485" xsd:double
-is_a: XLMOD:00097 ! oxidation cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00064 ! oxidized
-relationship: is_side_product_of XLMOD:02139 ! LC-SDA
-
-[Term]
-id: XLMOD:01084
-name: alkenized LC-SDA
-def: "Alkenized LC-SDA." [PSI:XL]
-property_value: deadEndFormula: "C10 H15 N1 O2" xsd:string
-property_value: monoIsotopicMass: "181.110278785" xsd:double
-is_a: XLMOD:00094 ! alkenization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00065 ! alkenized
-relationship: is_side_product_of XLMOD:02139 ! LC-SDA
-
-[Term]
-id: XLMOD:01085
-name: hydrolyzed L-Photo-Leucine
-def: "Hydrolyzed L-2-amino-4,4-azi-pentanoic acid." [PSI:XL]
-property_value: deadEndFormula: "-C1 -H2 O1" xsd:string
-property_value: monoIsotopicMass: "1.97926456" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:01900 ! L-Photo-Leucine
-
-[Term]
-id: XLMOD:01086
-name: oxidized L-Photo-Leucine
-def: "Oxidized L-2-amino-4,4-azi-pentanoic acid." [PSI:XL]
-property_value: deadEndFormula: "-C1 -H4 O1" xsd:string
-property_value: monoIsotopicMass: "-0.036385501" xsd:double
-is_a: XLMOD:00097 ! oxidation cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00064 ! oxidized
-relationship: is_side_product_of XLMOD:01900 ! L-Photo-Leucine
-
-[Term]
-id: XLMOD:01087
-name: alkenized L-Photo-Leucine
-def: "Alkenized L-2-amino-4,4-azi-pentanoic acid." [PSI:XL]
-property_value: deadEndFormula: "-C2 -H6" xsd:string
-property_value: monoIsotopicMass: "-30.04695021" xsd:double
-is_a: XLMOD:00094 ! alkenization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00065 ! alkenized
-relationship: is_side_product_of XLMOD:01900 ! L-Photo-Leucine
-
-[Term]
-id: XLMOD:01088
-name: hydrolyzed L-Photo-Methionine
-def: "Hydrolyzed L-2-amino-5,5-azi-hexanoic acid." [PSI:XL]
-property_value: deadEndFormula: "C1 H2 O1 -S1" xsd:string
-property_value: monoIsotopicMass: "-1.96150744" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:01901 ! L-Photo-Methionine
-
-[Term]
-id: XLMOD:01089
-name: oxidized L-Photo-Methionine
-def: "Oxidized L-2-amino-5,5-azi-hexanoic acid." [PSI:XL]
-property_value: deadEndFormula: "C1 O1 -S1" xsd:string
-property_value: monoIsotopicMass: "-3.97715607" xsd:double
-is_a: XLMOD:00097 ! oxidation cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00064 ! oxidized
-relationship: is_side_product_of XLMOD:01901 ! L-Photo-Methionine
-
-[Term]
-id: XLMOD:01090
-name: alkenized L-Photo-Methionine
-def: "Alkenized L-2-amino-5,5-azi-hexanoic acid." [PSI:XL]
-property_value: deadEndFormula: "-H2 -S1" xsd:string
-property_value: monoIsotopicMass: "-33.98772221" xsd:double
-is_a: XLMOD:00094 ! alkenization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00065 ! alkenized
-relationship: is_side_product_of XLMOD:01901 ! L-Photo-Methionine
-
-[Term]
-id: XLMOD:01091
-name: hydrolyzed BMOE
-def: "Hydrolyzed bis-Maleimidoethane." [PSI:XL]
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02188 ! BMOE
-
-[Term]
-id: XLMOD:01092
-name: hydrolyzed BMPS
-def: "Hydrolyzed N-(beta-Maleimidopropyloxy)succinimide ester." [PSI:XL]
-property_value: bridgeFormula: "C7 H7 O4 N1" xsd:string
-property_value: monoIsotopicMass: "169.037507765" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02013 ! BMPS
-
-[Term]
-id: XLMOD:01093
-name: ammonium amidated BMPS
-def: "Ammonium amidated N-(beta-Maleimidopropyloxy)succinimide ester." [PSI:XL]
-property_value: bridgeFormula: "C7 H8 O3 N2" xsd:string
-property_value: monoIsotopicMass: "168.05349217" xsd:double
-is_a: XLMOD:00095 ! ammonium amidation cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00021 ! ammonium amidated
-relationship: is_side_product_of XLMOD:02013 ! BMPS
-
-[Term]
-id: XLMOD:01094
-name: hydrolyzed PDH
-def: "Hydrolyzed pimelic acid dihydrazide." [PSI:XL]
-property_value: bridgeFormula: "C7 H12 N4" xsd:string
-property_value: monoIsotopicMass: "170.11676112" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02223 ! PDH
-
-[Term]
-id: XLMOD:01095
-name: hydrolyzed PDH-d10
-def: "Deuterium labelled hydrolyzed pimelic acid dihydrazide." [PSI:XL]
-property_value: bridgeFormula: "C7 D10 H2 N4" xsd:string
-property_value: doubletDeltaMass: "10.06276744" xsd:double
-property_value: monoIsotopicMass: "180.17952856" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02224 ! PDH-d10
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-
-[Term]
-id: XLMOD:01096
-name: hydrolyzed SuDP
-def: "Hydrolyzed disuccinimidyl-succinamyl-aspartyl-proline." [PMID:26091612]
-property_value: monoIsotopicMass: "294.0852" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02112 ! SuDP
-
-[Term]
-id: XLMOD:01097
-name: hydrolyzed L-Photo-Isoleucine
-def: "Hydrolyzed L-Photo-Isoleucine." [PSI:XL]
-property_value: deadEndFormula: "-C1 -H2 O1" xsd:string
-property_value: monoIsotopicMass: "1.97926456" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:01902 ! L-Photo-Isoleucine
-
-[Term]
-id: XLMOD:01098
-name: oxidized L-Photo-Isoleucine
-def: "Oxidized L-Photo-Isoleucine." [PSI:XL]
-property_value: deadEndFormula: "-C1 -H4 O1" xsd:string
-property_value: monoIsotopicMass: "-0.036385501" xsd:double
-is_a: XLMOD:00097 ! oxidation cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00064 ! oxidized
-relationship: is_side_product_of XLMOD:01902 ! L-Photo-Isoleucine
-
-[Term]
-id: XLMOD:01099
-name: alkenized L-Photo-Isoleucine
-def: "Alkenized L-Photo-Isoleucine." [PSI:XL]
-property_value: deadEndFormula: "-C2 -H6" xsd:string
-property_value: monoIsotopicMass: "-30.04695021" xsd:double
-is_a: XLMOD:00094 ! alkenization cross-linker related chemical modification
-relationship: is_partially_reacted XLMOD:00065 ! alkenized
-relationship: is_side_product_of XLMOD:01902 ! L-Photo-Isoleucine
-
-[Term]
-id: XLMOD:01100
-name: hydrolyzed Sulfo-SBED
-def: "Hydrolyzed Sulfo-SBED cross-linker." [PMID:16246579]
-property_value: monoIsotopicMass: "652.217" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:03002 ! Sulfo-SBED
-
-[Term]
-id: XLMOD:01101
-name: hydrolyzed PIR
-def: "Hydrolized Protein Interaction Reporter." [PMID:15623310]
-property_value: CID_Fragment: "828.5" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_cleavable XLMOD:00035 ! CID cleavable
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02237 ! PIR
-
-[Term]
-id: XLMOD:01102
-name: hydrolized PL
-def: "Hydrolyzed photo-cleavable Leiker." [PMID:26952210, PMID:27734140]
-property_value: monoIsotopicMass: "334.15" xsd:double
-is_a: XLMOD:00096 ! hydrolization cross-linker related chemical modification
-relationship: is_cleavable XLMOD:00147 ! photocleavable
-relationship: is_partially_reacted XLMOD:00011 ! hydrolyzed
-relationship: is_side_product_of XLMOD:02227 ! PL
-
-[Term]
-id: XLMOD:01700
-name: 8-methoxypsoralen
-def: "8-methoxypsoralen reagent." [CAS:298-81-7, PubChem_Compound:4114, ChemSpiderID:3971, ChemicalBookNo:CB6733540, PMID:9013628]
-synonym: "8-MOP" EXACT []
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-is_a: XLMOD:00100 ! reactive group
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-
-[Term]
-id: XLMOD:01701
-name: 4'-hydroxymethyl-4,5'8-trimethylpsoralen
-def: "4'-hydroxymethyl-4,5'8-trimethylpsoralen reagent." [CAS:62442-59-5, PubChem_Compound:104953, ChemSpiderID:94710, MDL:MFCD00036888, ChemicalBookNo:CB7358269, PMID:9013628]
-synonym: "HMT" EXACT []
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-is_a: XLMOD:00100 ! reactive group
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-
-[Term]
-id: XLMOD:01702
-name: 5-iodouracil
-def: "5-iodouracil reagent." [CAS:696-07-1, PubChem_Compound:69672, MDL:MFCD00006020, ChemSpiderID:62873, ChemicalBookNo:CB8771577, PMID:12476441, PMID:9013628]
-synonym: "5-IU" EXACT []
-synonym: "5IU" EXACT []
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-is_a: XLMOD:00081 ! nucleobase derivative
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-relationship: is_analog_of XLMOD:00080 ! uracil
-
-[Term]
-id: XLMOD:01703
-name: 4-thiouracil
-def: "4-thiouracil reagent." [CAS:591-28-6, PubChem_Compound:2734394, MDL:MFCD00090842, ChemSpiderID:2016146, ChemicalBookNo:CB4469328, PMID:12476441, PMID:22575267]
-synonym: "4-SU" EXACT []
-synonym: "4SU" EXACT []
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-is_a: XLMOD:00081 ! nucleobase derivative
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-relationship: is_analog_of XLMOD:00080 ! uracil
-
-[Term]
-id: XLMOD:01704
-name: 6-thioguanosine
-def: "6-thioguanosine reagent." [CAS:85-31-4, PubChem_Compound:2724387, ChemSpiderID:2006534, ChemicalBookNo:CB3722231, PMID:20946768, PMID:22575267]
-synonym: "6-SG" EXACT []
-synonym: "6SG" EXACT []
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-is_a: XLMOD:00088 ! nucleoside derivative
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-relationship: is_analog_of XLMOD:00084 ! guanosine
-
-[Term]
-id: XLMOD:01705
-name: 5-bromouracil
-def: "5-bromouracil reagent." [CAS:51-20-7, PubChem_Compound:5802, ChemSpiderID:5597, Beilstein:127176, MDL:MFCD00006017, ChemicalBookNo:CB6388195, PMID:9145285, PMID:22575267]
-synonym: "5-BU" EXACT []
-synonym: "5BU" EXACT []
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-is_a: XLMOD:00081 ! nucleobase derivative
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-relationship: is_analog_of XLMOD:00080 ! uracil
-
-[Term]
-id: XLMOD:01706
-name: 5-iodocytosine
-def: "5-iodocytosine reagent." [CAS:1122-44-7, PubChem_Compound:14281, MDL:MFCD00023162, ChemSpiderID:13643, ChemicalBookNo:CB9203633, PMID:9145285]
-synonym: "5-IC" EXACT []
-synonym: "5IC" EXACT []
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-is_a: XLMOD:00088 ! nucleoside derivative
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-relationship: is_analog_of XLMOD:00078 ! cytosine
-
-[Term]
-id: XLMOD:01707
-name: 8-azidoadenosine
-def: "8-azidoadenosine reagent." [CAS:4372-67-2, ChemSpiderID:141244, ChemicalBookNo:CB7166563, PMID:9145285]
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-is_a: XLMOD:00088 ! nucleoside derivative
-relationship: has_reactive_group XLMOD:00055 ! azide
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-relationship: is_analog_of XLMOD:00083 ! adenosine
-
-[Term]
-id: XLMOD:01708
-name: 2-azidoadenosine
-def: "2-azidoadenosine reagent." [CAS:59587-07-4, PubChem_Compound:510978, ChemicalBookNo:CB01175626, PMID:9145285]
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-is_a: XLMOD:00088 ! nucleoside derivative
-relationship: has_reactive_group XLMOD:00055 ! azide
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-relationship: is_analog_of XLMOD:00083 ! adenosine
-
-[Term]
-id: XLMOD:01709
-name: 8-azidoguanosine
-def: "8-azidoguanosine reagent." [PubChem_Compound:23375450, ChemSpiderID:8034117, PMID:9145285]
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-is_a: XLMOD:00088 ! nucleoside derivative
-relationship: has_reactive_group XLMOD:00055 ! azide
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-relationship: is_analog_of XLMOD:00084 ! guanosine
-
-[Term]
-id: XLMOD:01710
-name: 5-azidouridine
-def: "5-azidouridine reagent." [CAS:1261272-24-5, PubChem_Compound:20832934, ChemSpiderID:18697526, ChemicalBookNo:CB62543444, PMID:9145285]
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-is_a: XLMOD:00088 ! nucleoside derivative
-relationship: has_reactive_group XLMOD:00055 ! azide
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-relationship: is_analog_of XLMOD:00086 ! uridine
-
-[Term]
-id: XLMOD:01711
-name: bis-[3-(2-ketobutyraldehyde)ether
-def: "bis-[3-(2-ketobutyraldehyde)ether reagent." [CAS:84031-85-6, PubChem_Compound:134685, ChemSpiderID:118706, ChemicalBookNo:CB81338982, PMID:16875836]
-synonym: "Bikethoxal" EXACT []
-synonym: "BKT" EXACT []
-property_value: monoIsotopicMass: "230.079" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "5.4" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00115 ! glyoxal
-
-[Term]
-id: XLMOD:01712
-name: mechlorethamine
-def: "Mechlorethamine reagent." [CAS:55-86-7, PubChem_Compound:4033, MDL:MFCD00012517, ChemSpiderID:3893, ChemicalBookNo:CB5270716, PMID:16875836]
-synonym: "Nitrogen mustard" EXACT []
-synonym: "NM" EXACT []
-property_value: monoIsotopicMass: "83.073" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "9.5" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00153 ! chloroethyl
-
-[Term]
-id: XLMOD:01713
-name: 4-[bis-(2-chloroethyl)amino]benzenebutanoic acid
-def: "4-[bis-(2-chloroethyl)amino]benzenebutanoic acid reagent." [CAS:305-03-3, PubChem_Compound:2708, Beilstein:999011, MDL:MFCD00021783, ChemSpiderID:2607, ChemicalBookNo:CB5270716, PMID:16875836]
-synonym: "Chlorambucil" EXACT []
-synonym: "CHB" EXACT []
-property_value: monoIsotopicMass: "231.126" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "9.5" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00153 ! chloroethyl
-
-[Term]
-id: XLMOD:01714
-name: sym-triazine trichloride
-def: "Sym-triazine trichloride reagent." [CAS:108-80-5, PubChem_Compound:24851182, Beilstein:126982, MDL:MFCD00082990, ChemSpiderID:7668, ChemicalBookNo:CB5852763, PMID:16875836]
-synonym: "Cyanuric acid" EXACT []
-synonym: "STT" EXACT []
-property_value: monoIsotopicMass: "110.962" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "2.4" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-
-[Term]
-id: XLMOD:01715
-name: Heteroconjugate 20
-def: "Heteroconjugate 20 reagent." [PMID:26335278]
-synonym: "HC20" EXACT []
-property_value: monoIsotopicMass: "1554.6871" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! bifunctional cross-linker
-relationship: has_handle XLMOD:00051 ! biotin
-
-[Term]
-id: XLMOD:01716
-name: benzophenone-4-iodoacetamide
-def: "Benzophenone-4-iodoacetamide reagent." [CAS:76809-63-7, PubChem_Compound:131289, ChemicalBookNo:CB3488704, PMID:10208813]
-synonym: "BPI" EXACT []
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00119 ! benzophenone
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-
-[Term]
-id: XLMOD:01717
-name: azidophenacyl bromide
-def: "Azidophenacyl bromide reagent." [CAS:57018-46-9, PubChem_Compound:92627, Beilstein:1961705, MDL:MFCD00042637, ChemSpiderID:83619, ChemicalBookNo:CB3120420, PMID:10208813]
-synonym: "APB" EXACT []
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_fluorophore XLMOD:06110 ! phenacyl
-relationship: has_reactive_group XLMOD:00126 ! phenyl azide
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-
-[Term]
-id: XLMOD:01718
-name: benzophenone-phosphatidylcholine
-def: "Benzophenone-phosphatidylcholine." [PMID:19171301]
-synonym: "benzophenone-PC" EXACT []
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-is_a: XLMOD:00092 ! lipid analogue
-relationship: has_reactive_group XLMOD:00119 ! benzophenone
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-
-[Term]
-id: XLMOD:01719
-name: phenylazide-phosphatidylcholine
-def: "Phenylazide-phosphatidylcholine." [PMID:19171301]
-synonym: "phenylazide-PC" EXACT []
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-is_a: XLMOD:00092 ! lipid analogue
-relationship: has_reactive_group XLMOD:00126 ! phenyl azide
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-
-[Term]
-id: XLMOD:01720
-name: N-(4-azidosalicylamidyl)-1,2-dilauroyl-sn-glycero-3-phosphoethanolamine
-def: "The N-(4-azidosalicylamidyl)-1,2-dilauroyl-sn-glycero-3-phosphoethanolamine lipid analogue used for lipid-protein cross-linking." [PMID:19171301]
-synonym: "ASA" EXACT []
-is_a: XLMOD:00092 ! lipid analogue
-
-[Term]
-id: XLMOD:01721
-name: Ac5-5-SiaDAz
-def: "The Ac5-5-SiaDAz sialic acid analogue used for glycan-protein cross-linking." [PMID:18293988, PMID:19536272]
-is_a: XLMOD:00093 ! sialic acid analogue
-
-[Term]
-id: XLMOD:01722
-name: Ac4-ManNDAz
-def: "The Ac4-ManNDAz sialic acid analogue used for glycan-protein cross-linking." [PMID:18293988, PMID:19536272, PMID:20816498]
-is_a: XLMOD:00093 ! sialic acid analogue
-
-[Term]
-id: XLMOD:01723
-name: Ac4-ManNAc
-def: "The Ac4-ManNAc sialic acid analogue used for glycan-protein cross-linking." [PMID:19536272]
-is_a: XLMOD:00093 ! sialic acid analogue
-
-[Term]
-id: XLMOD:01724
-name: Ac4-GlcNDAz
-def: "The Ac4-GlcNDAz sialic acid analogue used for glycan-protein cross-linking." [PMID:19536272, PMID:20816498]
-is_a: XLMOD:00093 ! sialic acid analogue
-
-[Term]
-id: XLMOD:01725
-name: Ac5-methyl-SiaDAz
-def: "The Ac5-methyl-SiaDAz sialic acid analogue used for glycan-protein cross-linking." [PMID:20816498]
-is_a: XLMOD:00093 ! sialic acid analogue
-
-[Term]
-id: XLMOD:01726
-name: sialylated LacNAc-biotin
-def: "Sialylated LacNAc-biotin used for glycan-protein cross-linking." [PMID:26541974]
-is_a: XLMOD:00093 ! sialic acid analogue
-
-[Term]
-id: XLMOD:01800
-name: Psoralen-PEG3-Biotin
-def: "Psoralen-PEG3-Biotin biotinylation reagent." [PSI:XL]
-property_value: hydrophilicPEGchain: "3" xsd:nonNegativeInteger
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-property_value: spacerLength: "36.86" xsd:float
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00134 ! psoralen
-
-[Term]
-id: XLMOD:01801
-name: Photoactivatable Biotin
-def: "Photoactivatable Biotin biotinylation reagent." [PSI:XL]
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-property_value: spacerLength: "30.0" xsd:float
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_reactive_group XLMOD:00107 ! nitrophenyl azide
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-
-[Term]
-id: XLMOD:01802
-name: TFPA-PEG3-Biotin
-def: "TFPA-PEG3-Biotin biotinylation reagent." [CAS:1264662-85-2, ChemSpiderID:59757057]
-property_value: hydrophilicPEGchain: "3" xsd:nonNegativeInteger
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-property_value: spacerLength: "33.4" xsd:float
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00118 ! tetrafluorophenyl azide
-
-[Term]
-id: XLMOD:01803
-name: Biotin-LC-ASA
-def: "1-(4-azidosalicylamido)-6(biotinamido)-hexane." [ChemicalBookNo:CB9438943]
-synonym: "Biotin-Long Chain-ASA" EXACT []
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-property_value: spacerLength: "29.9" xsd:float
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_property XLMOD:00020 ! iodinatable
-relationship: has_reactive_group XLMOD:00125 ! hydroxyphenyl azide
-
-[Term]
-id: XLMOD:01804
-name: Sulfo-NHS-Biotin
-def: "Biotin 3-sulfo-N-hydroxysuccinimide ester sodium salt." [CAS:119616-38-5, PubChem_Compound:56846292, ChemSpiderID:28568147, ChemicalBookNo:CB8277468]
-synonym: "Sulfosuccinimidyl biotin" EXACT []
-synonym: "N-Hydroxysulfosuccinimidobiotin" EXACT []
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-property_value: spacerLength: "13.5" xsd:float
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-
-[Term]
-id: XLMOD:01805
-name: Sulfo-NHS-LC-Biotin
-def: "Sulfo-NHS-LC-Biotin biotinylation reagent." [CAS:127062-22-0, PubChem_Compound:71571497, ChemSpiderID:29788101, ChemicalBookNo:CB7387089]
-synonym: "Long chain Sulfo-NHS-Biotin" EXACT []
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-property_value: spacerLength: "22.4" xsd:float
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-
-[Term]
-id: XLMOD:01806
-name: NHS-PEG12-Biotin
-def: "NHS-PEG12-Biotin biotinylation reagent." [CAS:365441-71-0, PubChem_Compound:58481068, ChemSpiderID:29354431, ChemicalBookNo:CB52546796]
-synonym: "Biotin-PEG12-NHS ester" EXACT []
-property_value: hydrophilicPEGchain: "12" xsd:nonNegativeInteger
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-property_value: spacerLength: "56" xsd:float
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-
-[Term]
-id: XLMOD:01807
-name: NHS-SS-PEG4-Biotin
-def: "NHS-SS-PEG4-Biotin biotinylation reagent." [PSI:XL]
-property_value: hydrophilicPEGchain: "4" xsd:nonNegativeInteger
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-property_value: spacerLength: "37.9" xsd:float
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00023 ! cleavable S-S bond
-
-[Term]
-id: XLMOD:01808
-name: NHS-Biotin
-def: "Biotin N-hydroxysuccinimide ester." [CAS:35013-72-0, PubChem_Compound:434213, ChemSpiderID:5142865, ChemicalBookNo:CB7371998]
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-property_value: spacerLength: "13.5" xsd:float
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-
-[Term]
-id: XLMOD:01809
-name: NHS-LC-Biotin
-def: "Biotinamidohexanoyl-6-aminohexanoic acid N-hydroxysuccinimide ester." [CAS:89889-52-1, PubChem_Compound:4072290, ChemSpiderID:17346377, ChemicalBookNo:CB1412590]
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-property_value: spacerLength: "30.5" xsd:float
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-
-[Term]
-id: XLMOD:01810
-name: NHS-SS-Biotin
-def: "Biotin disulfide N-hydroxysuccinimide ester." [CAS:142439-92-7, PubChem_Compound:71312116, ChemSpiderID:3405732, ChemicalBookNo:CB4216304]
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-property_value: spacerLength: "24.3" xsd:float
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00023 ! cleavable S-S bond
-
-[Term]
-id: XLMOD:01811
-name: NHS-Iminobiotin trifluoroacetamide
-def: "NHS-Iminobiotin trifluoroacetamide biotinylation reagent." [ChemicalBookNo:CB6315012]
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-property_value: spacerLength: "13.5" xsd:float
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00071 ! iminobiotintrifluoroacetamide
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-
-[Term]
-id: XLMOD:01812
-name: PFP-Biotin
-def: "Pentafluorophenyl-Biotin." [CAS:120550-35-8, PubChem_Compound:11122445, ChemSpiderID:9297574, ChemicalBookNo:CB6307189]
-synonym: "Biotin-PFP-ester" EXACT []
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-property_value: spacerLength: "9.6" xsd:float
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_reactive_group XLMOD:00120 ! pentafluorophenyl
-
-[Term]
-id: XLMOD:01813
-name: TFP-PEG3-Biotin
-def: "Tetrafluorophenyl-PEG3-Biotin." [PSI:XL]
-property_value: hydrophilicPEGchain: "3" xsd:nonNegativeInteger
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-property_value: spacerLength: "32.6" xsd:float
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00150 ! tetrafluorophenyl ester
-
-[Term]
-id: XLMOD:01814
-name: Maleimide-PEG11-Biotin
-def: "Maleimide-PEG11-Biotin biotinylation reagent." [PSI:XL]
-property_value: hydrophilicPEGchain: "11" xsd:nonNegativeInteger
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-property_value: spacerLength: "59.1" xsd:float
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:01815
-name: Biotin-BMCC
-def: "1-Biotinamido-4-[4´-(maleimidomethyl)cyclohexanecarboxamido]butane." [ChemicalBookNo:CB5366406]
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-property_value: spacerLength: "32.6" xsd:float
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:01816
-name: Iodoacetyl-PEG2-Biotin
-def: "Iodoacetyl-PEG2-Biotin biotinylation reagent." [PSI:XL]
-property_value: hydrophilicPEGchain: "2" xsd:nonNegativeInteger
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-property_value: spacerLength: "24.7" xsd:float
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00127 ! iodoacetyl
-
-[Term]
-id: XLMOD:01817
-name: Iodoacetyl-LC-Biotin
-def: "Iodoacetyl-LC-Biotin biotinylation reagent." [CAS:93285-75-7, PubChem_Compound:125043, ChemSpiderID:4248811, ChemicalBookNo:CB5664328]
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-property_value: spacerLength: "27.1" xsd:float
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_reactive_group XLMOD:00127 ! iodoacetyl
-
-[Term]
-id: XLMOD:01818
-name: Pentylamine-Biotin
-def: "5-(Biotinamido)pentylamine." [CAS:115416-38-1, PubChem_Compound:83906, ChemSpiderID:75715, ChemicalBookNo:CB8415868]
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-property_value: spacerLength: "18.9" xsd:float
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00151 ! pentylamine
-
-[Term]
-id: XLMOD:01819
-name: Amine-PEG2-Biotin
-def: "5-(Biotinamido)pentylamine." [PubChem_Compound:11199678]
-synonym: "Biotin-PEG2-amine" EXACT []
-property_value: hydrophilicPEGchain: "2" xsd:nonNegativeInteger
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-property_value: spacerLength: "20.4" xsd:float
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00133 ! amine reactive group
-
-[Term]
-id: XLMOD:01820
-name: Amine-PEG3-Biotin
-def: "Amine-PEG3-Biotin biotinylation reagent." [PubChem_Compound:53384310]
-synonym: "Biotin-PEG3-amine" EXACT []
-property_value: hydrophilicPEGchain: "3" xsd:nonNegativeInteger
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-property_value: spacerLength: "22.9" xsd:float
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00133 ! amine reactive group
-
-[Term]
-id: XLMOD:01821
-name: Biocytine-Hydrazide
-def: "Biocytine-Hydrazide biotinylation reagent." [CS:102743-85-1, PubChem_Compound:128197]
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-property_value: spacerLength: "19.7" xsd:float
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00110 ! hydrazide
-
-[Term]
-id: XLMOD:01822
-name: Biotin-Hydrazide
-def: "Biocytine-Hydrazide biotinylation reagent." [CAS:66640-86-6, PubChem_Compound:83872, ChemSpiderID:75684, ChemicalBookNo:CB3175354]
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-property_value: spacerLength: "15.7" xsd:float
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_reactive_group XLMOD:00110 ! hydrazide
-
-[Term]
-id: XLMOD:01823
-name: Biotin-LC-Hydrazide
-def: "Long chain Biocytine-Hydrazide biotinylation reagent." [CAS:109276-34-8, PubChem_Compound:3504484, ChemSpiderID:75709, ChemicalBookNo:CB4309220]
-synonym: "Biotin-LC-Hz" EXACT []
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-property_value: spacerLength: "24.7" xsd:float
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00110 ! hydrazide
-
-[Term]
-id: XLMOD:01824
-name: Biotin-PEG4-Hydrazide
-def: "Biotin-PEG4-Hydrazide biotinylation reagent." [PubChem_Compound:51340934]
-property_value: hydrophilicPEGchain: "4" xsd:nonNegativeInteger
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-property_value: spacerLength: "31.3" xsd:float
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00110 ! hydrazide
-
-[Term]
-id: XLMOD:01825
-name: Photobiotin
-def: "Photoactivatable Biotin." [CAS:96087-37-5, PubChem_Compound:15949227, ChemSpiderID:2299671, ChemicalBookNo:CB7301795]
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-property_value: spacerLength: "30.0" xsd:float
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_reactive_group XLMOD:00107 ! nitrophenyl azide 
-
-[Term]
-id: XLMOD:01826
-name: Biotin-PEG2-Alkyne
-def: "Biotin-PEG2-Alkyne." [PubChem_Compound:91757772]
-property_value: hydrophilicPEGchain: "2" xsd:nonNegativeInteger
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_handle XLMOD:00053 ! alkyne
-relationship: is_cleavable XLMOD:00034 ! photo cleavable
-
-[Term]
-id: XLMOD:01827
-name: Biotin-PEG2-C4-Alkyne
-def: "Biotin-PEG2-C4-Alkyne." [CAS:109276-34-8, PubChem_Compound:91757769, ChemSpiderID:75709, ChemicalBookNo:CB73062389]
-property_value: hydrophilicPEGchain: "2" xsd:nonNegativeInteger
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_handle XLMOD:00053 ! alkyne
-relationship: is_cleavable XLMOD:00034 ! photo cleavable
-
-[Term]
-id: XLMOD:01828
-name: Biotin-PEG4-Alkyne
-def: "Biotin-PEG4-Alkyne." [CAS:1458576-00-5, PubChem_Compound:75409985, ChemicalBookNo:CB82984377]
-property_value: hydrophilicPEGchain: "4" xsd:nonNegativeInteger
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_handle XLMOD:00053 ! alkyne
-relationship: is_cleavable XLMOD:00034 ! photo cleavable
-
-[Term]
-id: XLMOD:01829
-name: 2-iminothiolane
-def: "2-iminothiolane reagent." [CAS:4781-83-3, PubChem_Compound:433941, MDL:MFCD00039013, ChemSpiderID:10732937, ChemicalBookNo:CB7373482, PMID:6170935, PMID:11350598]
-synonym: "Traut's reagent" EXACT []
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00154 ! imino
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-
-[Term]
-id: XLMOD:01830
-name: 3-Azidopyridine-adenine dinucleotide
-def: "3-Azidopyridine-adenine dinucleotide reagent." [CAS:50695-15-3, PubChem_Compound:189126, MDL:MFCD00078882, ChemSpiderID:164324, ChemicalBookNo:CB91349828, PMID:20946768, PMID:6770736]
-synonym: "APA" EXACT []
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00114 ! aryl azide
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-
-[Term]
-id: XLMOD:01900
-name: L-Photo-Leucine
-def: "L-2-amino-4,4-azi-pentanoic acid." [CAS:851960-91-3, ChemSpiderID:32980228, PMID:15782218, PMID:26700045]
-synonym: "L-Photo-Leu" EXACT []
-comment: A photoreactive amino acid analog of L-Leucine for incorporation during protein synthesis that can be used for in vivo labelling, cross-linking and protein-protein interaction studies in live cells.
-property_value: bridgeFormula: "-C1 -H4" xsd:string
-property_value: monoIsotopicMass: "-16.0313" xsd:double
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-is_a: XLMOD:00049 ! amino acid derivative
-relationship: has_reactive_group XLMOD:00103 ! diazirine
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-relationship: is_analog_of XLMOD:00059 ! L-Leucine
-
-[Term]
-id: XLMOD:01901
-name: L-Photo-Methionine
-def: "L-2-amino-5,5-azi-hexanoic acid." [CAS:851960-68-4, ChemSpiderID:61327213, PMID:15782218, PMID:26700045]
-synonym: "L-Photo-Met" EXACT []
-comment: A photoreactive amino acid analog of L-Methionine for incorporation during protein synthesis that can be used for in vivo labelling, cross-linking and protein-protein interaction studies in live cells.
-property_value: bridgeFormula: "C1 -S1" xsd:string
-property_value: monoIsotopicMass: "-19.972072" xsd:double
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-is_a: XLMOD:00049 ! amino acid derivative
-relationship: has_reactive_group XLMOD:00103 ! diazirine
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-relationship: is_analog_of XLMOD:00060 ! L-Methionine
-
-[Term]
-id: XLMOD:01902
-name: L-Photo-Isoleucine
-def: "L-Photo-Isoleucine." [PMID:16477643]
-synonym: "L-Photo-Ile" EXACT []
-comment: A photoreactive amino acid analog of L-Isoleucine for incorporation during protein synthesis that can be used for in vivo labelling, cross-linking and protein-protein interaction studies in live cells.
-property_value: bridgeFormula: "-C1 -H4" xsd:string
-property_value: monoIsotopicMass: "-16.0313" xsd:double
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-is_a: XLMOD:00049 ! amino acid derivative
-relationship: has_reactive_group XLMOD:00103 ! diazirine
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-relationship: is_analog_of XLMOD:00068 ! L-Isoleucine
-
-[Term]
-id: XLMOD:01903
-name: pBpa
-def: "p-benzoyl-L-phenylalanine." [PMID:16170867]
-comment: A photoreactive amino acid analog of L-Phenylalanine for incorporation during protein synthesis that can be used for in vivo labelling, cross-linking and protein-protein interaction studies in live cells.
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-is_a: XLMOD:00049 ! amino acid derivative
-relationship: has_reactive_group XLMOD:00119 ! benzophenone
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-relationship: is_analog_of XLMOD:00070 ! L-Phenylalanine
-
-[Term]
-id: XLMOD:01904
-name: pBpa-d11
-def: "Deuterium labelled p-benzoyl-L-phenylalanine." [PMID:18704231]
-comment: A photoreactive deuterium-labelled amino acid analog of L-Phenylalanine for incorporation during protein synthesis that can be used for in vivo labelling, cross-linking and protein-protein interaction studies in live cells.
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-is_a: XLMOD:00049 ! amino acid derivative
-relationship: has_reactive_group XLMOD:00119 ! benzophenone
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-relationship: is_analog_of XLMOD:00070 ! L-Phenylalanine
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-
-[Term]
-id: XLMOD:02000
-name: BS3
-def: "Bis(sulfosuccinimidyl)suberate." [CAS:82436-77-9, PubChem_Compound:6097991, PMID:12892908, ChemSpiderID:110394, ChemicalBookNo:CB0136444]
-synonym: "Suberic acid bis(3-sulfo-N-hydroxysuccinimide ester)" EXACT []
-synonym: "Bis(sulfosuccinimidyl)suberate" EXACT []
-synonym: "Sulfo-DSS" EXACT []
-synonym: "BSSS" EXACT []
-synonym: "BS3-d0" EXACT []
-synonym: "BS3-H12" EXACT []
-property_value: bridgeFormula: "C8 H10 O2" xsd:string
-property_value: monoIsotopicMass: "138.06807961" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "11.4" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-
-[Term]
-id: XLMOD:02001
-name: DSS
-def: "Disuccinimidyl suberate." [CAS:68528-80-3, PubChem_Compound:100658, PMID:16944939, ChemSpiderID:90944, ChemicalBookNo:CB1219157]
-synonym: "Bis(succinimidyl) suberate" EXACT []
-synonym: "Suberic acid bis(N-hydroxysuccinimide ester)" EXACT []
-synonym: "Disuccinimidyl octanedioate" EXACT []
-synonym: "DSS-d0" EXACT []
-synonym: "DSS-H12" EXACT []
-synonym: "1,1'-[(1,8-Dioxooctane-1,8-diyl)bis(oxy)]dipyrrolidine-2,5-dione" EXACT []
-property_value: bridgeFormula: "C8 H10 O2" xsd:string
-property_value: monoIsotopicMass: "138.06807961" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "11.4" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-
-[Term]
-id: XLMOD:02002
-name: DSS-d4
-def: "Deuterium labelled disuccinimidyl 2,2,7,7-suberate." [PubChem_Compound:91757798, PMID:11354472]
-property_value: bridgeFormula: "C8 D4 H6 O2" xsd:string
-property_value: doubletDeltaMass: "4.02508" xsd:double
-property_value: monoIsotopicMass: "142.093186586" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "11.4" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-
-[Term]
-id: XLMOD:02003
-name: DSS-d12
-def: "Deuterium labelled disuccinimidyl 2,2,3,3,4,4,5,5,6,6,7,7-suberate." [PSI:XL, PMID:11354472, PMID:16944939]
-property_value: bridgeFormula: "C8 D10 O2" xsd:string
-property_value: doubletDeltaMass: "12.07573" xsd:double
-property_value: monoIsotopicMass: "150.143400538" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "11.4" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-
-[Term]
-id: XLMOD:02004
-name: BS3-d4
-def: "Deuterium labelled (bis(sulfosuccinimidyl) 2,2,7,7-suberate)." [PubChem_Compound:91757801]
-property_value: doubletDeltaMass: "4.02508" xsd:double
-property_value: monoIsotopicMass: "142.093186586" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "11.4" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-
-[Term]
-id: XLMOD:02005
-name: BS2G
-def: "Bis(sulfosuccinimidyl) glutarate." [PubChem_Compound:91757794, ChemicalBookNo:CB91307211]
-synonym: "Glutaric acid bis(3-sulfo-N-hydroxysuccinimide ester)" EXACT []
-synonym: "Sulfo-DSG" EXACT []
-synonym: "Disulfosuccinimidylglutarate" EXACT []
-synonym: "DSSG" EXACT []
-synonym: "BS2G-d0" EXACT []
-property_value: bridgeFormula: "C5 H4 O2" xsd:string
-property_value: monoIsotopicMass: "96.0211294" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "7.7" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-
-[Term]
-id: XLMOD:02006
-name: DSG
-def: "Disuccinimidyl glutarate." [CAS:79642-50-5, PubChem_Compound:4432628, Beilstein:8575145, MDL:MFCD00153597, ChemSpiderID:3632504, ChemicalBookNo:CB0373852]
-synonym: "Di(N-succinimidyl) glutarate" EXACT []
-synonym: "Di-succinimidyl glutarate" EXACT []
-synonym: "Di N-succinimidyl glutarate" EXACT []
-synonym: "Bis-NHS glutarate" EXACT []
-synonym: "Disuccinimidyl glutaric dicarboxylate" EXACT []
-synonym: "DSG-d0" EXACT []
-property_value: bridgeFormula: "C5 H4 O2" xsd:string
-property_value: monoIsotopicMass: "96.0211294" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "7.7" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-
-[Term]
-id: XLMOD:02007
-name: DSG-d4
-def: "Deuterium labelled disuccinimidyl 2,2,4,4-glutarate." [PubChem_Compound:91757797]
-property_value: bridgeFormula: "C5 D4 O2" xsd:string
-property_value: doubletDeltaMass: "4.02508" xsd:double
-property_value: monoIsotopicMass: "100.046236376" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "7.7" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-
-[Term]
-id: XLMOD:02008
-name: BS2G-d4
-def: "Deuterium labelled bis(sulfosuccinimidyl) 2,2,4,4-glutarate." [PubChem_Compound:91757799]
-synonym: "DSSG-d4" EXACT []
-property_value: bridgeFormula: "C5 D4 O2" xsd:string
-property_value: doubletDeltaMass: "4.02508" xsd:double
-property_value: monoIsotopicMass: "100.046236376" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "7.7" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-
-[Term]
-id: XLMOD:02009
-name: Disulfide
-def: "Disulfide." [PSI:XL]
-property_value: bridgeFormula: "-H2" xsd:string
-property_value: monoIsotopicMass: "-2.01565007" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: specificities: "(C)&(C)" xsd:string
-is_a: XLMOD:00005 ! homofunctional cross-linker
-is_a: XLMOD:00008 ! zero-length cross-linker
-
-[Term]
-id: XLMOD:02010
-name: 1-ethyl-3-(3-Dimethylaminopropyl)carbodiimide hydrochloride
-def: "1-ethyl-3-(3-Dimethylaminopropyl)carbodiimide hydrochloride." [CAS:25952-53-8, PubChem_Compound:2723939, Beilstein:5764110, ChemSpiderID:2006116, ChemicalBookNo:CB7403031, MDL:MFCD00012503, PMID:19136724, PMID:3394930]
-comment: Used to conjugate carboxyl functional groups to primary amines from peptides and proteins and is ideal for covalently binding proteins or peptides to carboxyl containing beads, resins, or nanoparticles.
-synonym: "3-(3-Dimethylaminopropyl)-1-ethyl-carbodiimide hydrochloride" EXACT []
-synonym: "EDAC-HCl" EXACT []
-synonym: "EDCI" EXACT []
-synonym: "EDC-HCl" EXACT []
-property_value: bridgeFormula: "-H2 -O1" xsd:string
-property_value: monoIsotopicMass: "-18.01056027" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00008 ! zero-length cross-linker
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00105 ! Carbodiimide
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:02011
-name: BDP-NHP
-def: "Biotin Aspartate Proline n-hydroxyphthalamide." [PSI:XL]
-property_value: monoIsotopicMass: "1241.469925525" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: is_cleavable XLMOD:00018 ! cleavable by MS2 labile bond
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_reactive_group XLMOD:00104 ! N-hydroxyphthalimide
-
-[Term]
-id: XLMOD:02012
-name: ANB-NOS
-def: "N-5-Azido-2-nitrobenzoyloxysuccinimide." [CAS:60117-35-3, PubChem_Compound:3080866, Beilstein:1555224, MDL:MFCD00054962, ChemSpiderID:2338587, ChemicalBookNo:CB7381289]
-synonym: "N-Succinimidyl 5-azido-2-nitrobenzoate" EXACT []
-synonym: "5-Azido-2-nitrobenzoic acid N-hydroxysuccinimide ester" EXACT []
-synonym: "N-(5-Azido-2-nitrobenzoyloxy)succinimide" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "7.7" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00107 ! nitrophenyl azide
-
-[Term]
-id: XLMOD:02013
-name: BMPS
-def: "N-(beta-Maleimidopropyloxy)succinimide ester." [CAS:55750-62-4, PubChem_Compound:4620597, Beilstein:1492578, MDL:MFCD00043141, ChemSpiderID:3811455, ChemicalBookNo:CB5780592]
-synonym: "N-Succinimidyl 3-maleimidopropionate" EXACT []
-synonym: "3-Maleimidopropionic acid N-hydroxysuccinimide ester" EXACT []
-property_value: bridgeFormula: "C7 H5 O3 N1" xsd:string
-property_value: monoIsotopicMass: "151.026943065" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "6.9" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:02014
-name: EMCS
-def: "6-Maleimidohexanoic acid N-hydroxysuccinimide ester." [CAS:55750-63-5, PubChem_Compound:5091655, ChemSpiderID:4267588, ChemicalBookNo:CB8212960]
-synonym: "N-(epsilon-Malaimidocaproyloxy) succinimide ester" EXACT []
-synonym: "6-maleimidohexanoic acid N-hydroxysuccinimide ester" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "9.4" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:02015
-name: GMBS
-def: "N-[gamma-Maleimidobutyryloxy] succinimide." [CAS:80307-12-6, PubChem_Compound:133440, MDL:MFCD00036817, ChemSpiderID:117712, ChemicalBookNo:CB5267080]
-synonym: "4-Maleimdobutyric acid N-succinimidyl ester" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "7.3" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:02016
-name: SPDP
-def: "N-Succinimidyl 3-[2-pyridyldithio]-propionate." [CAS:68181-17-9, PubChem_Compound:100682, ChemSpiderID:90967, ChemicalBookNo:CB2446059]
-synonym: "3-(2-Pyridyldithio)propionic acid N-hydroxysuccinimide ester" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "6.8" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00109 ! pyridinyldisulfide
-
-[Term]
-id: XLMOD:02017
-name: LC-SPDP
-def: "Succinimidyl 6-(3-[2-pyridyldithio]-propionamido)hexanoate." [CAS:158913-22-5, PubChem_Compound:157808, ChemSpiderID:138854, ChemicalBookNo:CB8355139]
-synonym: "Long chain-SPDP" EXACT []
-synonym: "Succinimidyl 6-(3-(2-Pyridyldithio)propionamido)hexanoate" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "15.7" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00109 ! pyridinyldisulfide
-
-[Term]
-id: XLMOD:02018
-name: Sulfo-LC-SPDP
-def: "Sulfosuccinimidyl 6-(3'-[2-pyridyldithio]-propionamido)hexanoate." [CAS:169751-10-4, PubChem_Compound:4588467, ChemSpiderID:3780707, ChemicalBookNo:CB8177681]
-synonym: "Sulfo-Long chain-SPDP" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "15.7" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: has_reactive_group XLMOD:00109 ! pyridinyldisulfide
-
-[Term]
-id: XLMOD:02019
-name: MBS
-def: "m-Maleimidobenzoyl-N-hydroxysuccinimide ester." [CAS:58626-38-3, PubChem_Compound:93861, ChemSpiderID:84714, ChemicalBookNo:CB0342553]
-synonym: "3-Maleimidobenzoic acid N-hydroxysuccinimide ester" EXACT []
-synonym: "meta-Maleimidobenzoyl-N-hydroxysuccinimide ester" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "7.3" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:02020
-name: Sulfo-MBS
-def: "m-Maleimidobenzoyl-N-hydroxysulfosuccinimide ester." [CAS:92921-25-0, ChemSpiderID:111159, ChemicalBookNo:CB9338287]
-synonym: "3-Maleimidobenzoic acid N-hydroxysulfosuccinimide ester" EXACT []
-synonym: "meta-Maleimidobenzoyl-N-hydroxysulfosuccinimide ester" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "7.3" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:02021
-name: PDPH
-def: "3-[2-Pyridyldithio]propionyl hydrazide." [CAS:115616-51-8, PubChem_Compound:130785, ChemSpiderID:115670, ChemicalBookNo:CB3412468]
-synonym: "SPDP Hydrazide" EXACT []
-synonym: "S-(2-thiopyridyl)-3-mercaptopropionic acid hydrazide" EXACT []
-synonym: "3-(2-pyridyldithio)propionyl hydrazide" EXACT []
-synonym: "TPMPH" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "9.2" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00109 ! pyridinyldisulfide
-relationship: has_reactive_group XLMOD:00110 ! hydrazide
-
-[Term]
-id: XLMOD:02022
-name: SBA
-def: "N-Succinimidyl bromoacetate." [CAS:42014-51-7, PubChem_Compound:3565210, ChemSpiderID:2802588, ChemicalBookNo:CB4678610]
-synonym: "Bromoacetic acid N-hydroxysuccinimide ester" EXACT []
-synonym: "Succinimidyl bromoacetate" EXACT []
-synonym: "NHS-Bromoacetate" EXACT []
-synonym: "SIB" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "1.5" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00128 ! bromoacetyl
-
-[Term]
-id: XLMOD:02023
-name: SIA
-def: "N-Succinimidyl iodoacetate." [CAS:39028-27-8, PubChem_Compound:3299230, ChemSpiderID:2547635, ChemicalBookNo:CB9364435]
-synonym: "Iodoacetic acid N-hydroxysuccinimide ester" EXACT []
-synonym: "Succinimidyl iodoacetate" EXACT []
-synonym: "NHS-Iodoacetate" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "1.5" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00127 ! iodoacetyl
-
-[Term]
-id: XLMOD:02024
-name: SMCC
-def: "Succinimidyl-4-[N-maleimidomethyl]cyclohexane-1-carboxylate." [CAS:64987-85-5, PubChem_Compound:125175, ChemSpiderID:21173480, ChemicalBookNo:CB6748487]
-synonym: "4-(N-Maleimidomethyl)cyclohexanecarboxylic acid N-hydroxysuccinimide ester" EXACT []
-synonym: "N-Succinimidyl 4-(maleimidomethyl)cyclohexanecarboxylate" EXACT []
-synonym: "Succinimidyl trans-4-(N-maleimidylmethyl)cyclohexane-1-carboxylate" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "11.6" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:02025
-name: Sulfo-SMCC
-def: "Sulfosuccinimidyl-4-[N-maleimidomethyl]cyclohexane-1-carboxylate." [CAS:92921-24-9, PubChem_Compound:16219679, ChemSpiderID:3809728, ChemicalBookNo:CB6219112]
-synonym: "4-(N-Maleimidomethyl)cyclohexane-1-carboxylic acid 3-sulfo-N-hydroxysuccinimide ester" EXACT []
-synonym: "Sulfosuccinimidyl-4-N-maleimidomethyl-cyclohexane-1-carboxylate" EXACT []
-synonym: "SSMCC" EXACT []
-synonym: "S-SMCC" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "11.6" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:02026
-name: SMPB
-def: "N-Succinimidyl 4-[4-maleimidophenyl]butyrate." [CAS:79886-55-8, PubChem_Compound:100681, ChemSpiderID:90966, ChemicalBookNo:CB3322684]
-synonym: "4-(4-Maleimidophenyl)butyric acid N-hydroxysuccinimide ester" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "11.6" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:02027
-name: SMPH
-def: "Succinimidyl-6-[beta-maleimidopropionamido]hexanoate." [CAS:367927-39-7, PubChem_Compound:4170355, ChemSpiderID:3381798, ChemicalBookNo:CB2100210]
-synonym: "Succinimidyl 6-[(3-maleimido)propionamido]-hexanoate" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "14.3" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-relationship: is_cleavable XLMOD:00041 ! thiol cleavable
-
-[Term]
-id: XLMOD:02028
-name: Sulfo-SANPAH
-def: "N-Sulfosuccinimidyl-6-[4'-azido-2'-nitrophenylamino] hexanoate." [CAS:102568-43-4, PubChem_Compound:3035866, ChemSpiderID:2300000, ChemicalBookNo:CB4457477]
-synonym: "1-[6-[(4-azido-2-nitro-phenyl)amino]hexanoyloxy]-2,5-Dioxo-pyrrolidine-3-sulfonic acid" EXACT []
-synonym: "Sulfosuccinimidyl 6-((4-azido-2-nitrophenyl)amino)hexanoate" EXACT []
-synonym: "Sulfosuccinimidyl 6-((4'-azido-2'-nitrophenyl)amino)hexanoate" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "18.2" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: has_reactive_group XLMOD:00107 ! nitrophenyl azide 
-
-[Term]
-id: XLMOD:02029
-name: DSP
-def: "Dithiobis[succinimidyl propionate." [CAS:57757-57-0, PubChem_Compound:93313, Beilstein:1518074, MDL:MFCD00042045, ChemSpiderID:84243, ChemicalBookNo:CB7251791]
-synonym: "3,3'-Dithiodipropionic acid di(N-hydroxysuccinimide ester)" EXACT []
-synonym: "Di(N-succinimidyl) 3,3'-Dithiodipropionate" EXACT []
-synonym: "Dithiobis-succinimidyl propionate" EXACT []
-synonym: "Dithio-bis-succinimidyl propionate" EXACT []
-synonym: "Dithiobis(succinimidyl propionate)" EXACT []
-synonym: "Lomant's Reagent" EXACT []
-synonym: "DTSP" EXACT []
-synonym: "DSP-d0" EXACT []
-property_value: bridgeFormula: "C6 H6 O2 S2" xsd:string
-property_value: monoIsotopicMass: "173.98092087" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "12.0" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00023 ! cleavable S-S bond
-
-[Term]
-id: XLMOD:02030
-name: DSP-d8
-def: "Deuterium labelled Dithiobis[1,1,2,2,2,2,3,3-succinimidyl propionate." [PubChem_Compound:91757796]
-property_value: bridgeFormula: "C6 D6 O2 S2" xsd:string
-property_value: doubletDeltaMass: "8.05016" xsd:double
-property_value: monoIsotopicMass: "182.0314167" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "12.0" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00023 ! cleavable S-S bond
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-
-[Term]
-id: XLMOD:02031
-name: DSSeb
-def: "Sebacic acid bis[N-hydroxysuccinimide ester]." [CAS:23024-29-5, PubChem_Compound:3430836, ChemSpiderID:2674029, ChemicalBookNo:CB4402699]
-synonym: "Disuccinimidyl sebacate" EXACT []
-synonym: "Sebacic acid bis(N-hydroxysuccinimide ester)" EXACT []
-synonym: "Di(N-succinimidyl) sebacate" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "14.1" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-
-[Term]
-id: XLMOD:02032
-name: DST
-def: "Disuccinimidyl tartrate." [CAS:62069-75-4, PubChem_Compound:124912, MDL:MFCD03788224, ChemSpiderID:296442, ChemicalBookNo:CB9243998]
-synonym: "Disuccinimidyl L-Tartrate" EXACT []
-property_value: bridgeFormula: "C4 H2 O4" xsd:string
-property_value: monoIsotopicMass: "113.99531" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "6.4" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00024 ! periodate cleavable
-
-[Term]
-id: XLMOD:02033
-name: DTSSP
-def: "3,3'-Dithiobis[sulfosuccinimidylpropionate]." [CAS:81069-02-5, PubChem_Compound:123933, MDL:MFCD01861949, ChemSpiderID:110462, ChemicalBookNo:CB31073260, PMID:10975572, PMID:18510349]
-synonym: "3,3'-Dithiobispropionic Acid Bis-sulfosuccinimidyl Ester" EXACT []
-synonym: "Sulfo-DSP" EXACT []
-synonym: "Sulfo-DTSP" EXACT []
-synonym: "DTBSSP" EXACT []
-synonym: "DTSSP-d0" EXACT []
-property_value: bridgeFormula: "C6 H6 O2 S2" xsd:string
-property_value: monoIsotopicMass: "173.98093" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "12.0" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: is_cleavable XLMOD:00023 ! cleavable S-S bond
-
-[Term]
-id: XLMOD:02034
-name: EGS
-def: "Ethylene glycolbis(succinimidylsuccinate)." [CAS:70539-42-3, PubChem_Compound:123663, ChemSpiderID:110243, ChemicalBookNo:CB5722624]
-synonym: "Ethylene glycol bis (succinimidylsuccinate)" EXACT []
-synonym: "Ethylene Glycol-Bis (Succinic Acid N-Hydroxysuccinimide Ester)" EXACT []
-synonym: "EGS-d0" EXACT []
-property_value: bridgeFormula: "C10 H10 O6" xsd:string
-property_value: monoIsotopicMass: "226.047738" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "16.1" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00025 ! hydroxylamine cleavable
-relationship: is_cleavable XLMOD:00039 ! ammonium cleavable
-
-[Term]
-id: XLMOD:02035
-name: Sulfo-EGS
-def: "Ethylene glycolbis(sulfosuccinimidylsuccinate)." [CAS:167410-92-6, PubChem_Compound:91757793, ChemSpiderID:32034171, ChemicalBookNo:CB4497176]
-synonym: "Ethylene glycol bis(sulfosuccinimidylsuccinate)" EXACT []
-synonym: "Ethylene Glycol-Bis (Succinic Acid N-Hydroxysulfosuccinimide Ester)" EXACT []
-synonym: "Bis(sulfo-N-succinimidyl) ethylene glycol disuccinate" EXACT []
-synonym: "Ethylene glycol disuccinate bis(sulfo-N-succinimidyl) ester" EXACT []
-synonym: "EGSS" EXACT []
-synonym: "EGSS-d0" EXACT []
-property_value: bridgeFormula: "C10 H10 O6" xsd:string
-property_value: monoIsotopicMass: "226.04774" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "16.1" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: is_cleavable XLMOD:00025 ! hydroxylamine cleavable
-relationship: is_cleavable XLMOD:00039 ! ammonium cleavable
-
-[Term]
-id: XLMOD:02036
-name: CDI
-def: "N,N'-Carbonyldiimidazole." [CAS:530-62-1, PubChem_Compound:68263, Beilstein:6826, MDL:MFCD00005286, ChemSpiderID:61561, ChemicalBookNo:CB0215374]
-comment: Used to convert alcohols and amines into carbamates, esters, and ureas.
-synonym: "1,1'-Carbonyldiimidazole" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00008 ! zero-length cross-linker
-
-[Term]
-id: XLMOD:02037
-name: DCC
-def: "N,N'-Dicyclohexylcarbodiimide." [CAS:538-75-0, PubChem_Compound:10868, Beilstein:610662, MDL:MFCD00011659, ChemSpiderID:10408, ChemicalBookNo:CB9706578]
-comment: Used for coupling amines and carboxylates without the insertion of spacer atoms.
-synonym: "DCCD" EXACT []
-synonym: "DCCI" EXACT []
-synonym: "Bis(cyclohexyl)carbodiimide" EXACT []
-synonym: "Cyclohexaamine, N,N'-methanetetraylbis-(9CI)" EXACT []
-synonym: "Dicyclohexylcarbodiimide" EXACT []
-synonym: "N,N'-Dicyclohexylcarbodiimide" EXACT []
-synonym: "1,3-Dicyclohexylcarbodiimide" EXACT []
-synonym: "N,N'-Methanetetrayl biscyclohexanamine" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00008 ! zero-length cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00105 ! Carbodiimide
-
-[Term]
-id: XLMOD:02038
-name: NHS
-def: "N-hydroxysuccinimide." [CAS:6066-82-6, PubChem_Compound:80170, Beilstein:113913, MDL:MFCD00005516, ChemSpiderID:72416, ChemicalBookNo:CB0391283]
-comment: Used in conjunction with EDC-HCl (EDAC-HCl) to convert carboxyl groups to NHS esters which react with primary amines.
-synonym: "1-Hydroxy-2,5-pyrrolidinedione" EXACT []
-is_a: XLMOD:00008 ! zero-length cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-
-[Term]
-id: XLMOD:02039
-name: Sulfo-NHS
-def: "N-hydroxysulfosuccinimide." [CAS:106627-54-7, PubChem_Compound:3520574, MDL:MFCD00043100, ChemSpiderID:2759874, ChemicalBookNo:CB9164497]
-comment: Used in conjunction with EDC-HCl (EDAC-HCl) to convert carboxyl groups to Sulfo-NHS esters which react with primary amines.
-synonym: "Sulfo NHS" EXACT []
-synonym: "S-NHS" EXACT []
-synonym: "Hydroxy-2,5-Dioxopyrrolidine-3-sulfonicacid" EXACT []
-is_a: XLMOD:00008 ! zero-length cross-linker
-relationship: has_property XLMOD:00014 ! hydrophilic
-
-[Term]
-id: XLMOD:02040
-name: BiPS
-def: "Bimane bisthiopropionic acid N-succinimidyl ester." [PMID:18838738]
-property_value: bridgeFormula: "C16 H16 N2 O4 S2" xsd:string
-property_value: monoIsotopicMass: "364.05515" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_property XLMOD:00015 ! fluorescent
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00034 ! photo cleavable
-
-[Term]
-id: XLMOD:02041
-name: formaldehyde
-def: "Formaldehyde reagent." [CAS:50-00-0, ChemSpiderID:692, ChemicalBookNo:CB4853677, PMID:18438963, PMID:25979347]
-property_value: reactionSites: "1" xsd:nonNegativeInteger
-property_value: spacerLength: "2.5" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00116 ! aldehyde
-relationship: is_reactive_with XLMOD:00037 ! non-selective
-
-[Term]
-id: XLMOD:02042
-name: glutardialdehyde
-def: "Glutardialdehyde." [CAS:111-30-8, ChemSpiderID:3365, ChemicalBookNo:CB3762723]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00116 ! aldehyde
-relationship: is_reactive_with XLMOD:00037 ! non-selective
-
-[Term]
-id: XLMOD:02043
-name: DSA
-def: "Disuccinimidyladipic acid." [CAS:26544-38-7, PubChem_Compound:6438029, ChemSpiderID:4515188, ChemicalBookNo:CB5470426]
-synonym: "disuccinimidyl adipate" EXACT []
-property_value: bridgeFormula: "C6 H6 O2" xsd:string
-property_value: monoIsotopicMass: "110.03624" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-
-[Term]
-id: XLMOD:02044
-name: DNBDPS
-def: "An isotopically-coded cleavable crosslinker affinity-purifyable with antibodies." [PMID:20109223]
-property_value: bridgeFormula: "C12 H9 N2 O6 S2" xsd:string
-property_value: monoIsotopicMass: "339.98238" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_handle XLMOD:00054 ! DNB
-relationship: is_cleavable XLMOD:00023 ! cleavable S-S bond
-
-[Term]
-id: XLMOD:02045
-name: TEABS
-def: "TEABS cross-linking reagent." [PMID:20109223]
-property_value: bridgeFormula: "C28 H39 N5 O11 S1" xsd:string
-property_value: monoIsotopicMass: "653.23668" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: is_cleavable XLMOD:00038 ! DTT cleavable
-relationship: is_cleavable XLMOD:00039 ! ammonium cleavable
-
-[Term]
-id: XLMOD:02046
-name: CLIP
-def: "Click-enabled linker for interacting proteins." [PMID:19496583]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "9.5" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_handle XLMOD:00053 ! alkyne
-relationship: has_neutral_loss_reporter XLMOD:00052 ! NO2 neutral loss reporter
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-
-[Term]
-id: XLMOD:02047
-name: BDRG
-def: "Biotin-aspartate-Rink-glycine cross-linker composed of a biotin affinity handle (B), a pentafluorophenyl (PFP) ester modified aspartate reside (D), a Rink group (R), and a PFP ester modified glycine reside (G)." [PMID:22067100]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: is_cleavable XLMOD:00018 ! cleavable by MS2 labile bond
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_reactive_group XLMOD:00120 ! pentafluorophenyl
-
-[Term]
-id: XLMOD:02048
-name: DTSSP-d8
-def: "Deuterium labelled 3,3'-Dithiobis[sulfosuccinimidylpropionate]." [PMID:10975572, PMID:18510349]
-property_value: bridgeFormula: "C6 D6 O2 S2" xsd:string
-property_value: doubletDeltaMass: "8.05016" xsd:double
-property_value: monoIsotopicMass: "182.03109" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "12.0" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: is_cleavable XLMOD:00023 ! cleavable S-S bond
-relationship: is_cleavable XLMOD:00035 ! CID cleavable
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-
-[Term]
-id: XLMOD:02049
-name: EGS-d12
-def: "Deuterium labelled ethylene glycolbis(succinimidylsuccinate)." [PMID:15901824]
-property_value: bridgeFormula: "C10 D10 O6" xsd:string
-property_value: doubletDeltaMass: "12.07573" xsd:double
-property_value: monoIsotopicMass: "238.12347" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "16.1" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00025 ! hydroxylamine cleavable
-relationship: is_cleavable XLMOD:00039 ! ammonium cleavable
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-
-[Term]
-id: XLMOD:02050
-name: Sulfo-EGS-d12
-def: "Deuterium labelled ethylene glycolbis(sulfosuccinimidylsuccinate)." [PMID:15901824]
-property_value: bridgeFormula: "C10 D10 O6" xsd:string
-property_value: doubletDeltaMass: "12.07573" xsd:double
-property_value: monoIsotopicMass: "238.12347" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "16.1" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: is_cleavable XLMOD:00025 ! hydroxylamine cleavable
-relationship: is_cleavable XLMOD:00039 ! ammonium cleavable
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-
-[Term]
-id: XLMOD:02051
-name: PCAS
-def: "Pyridine-3-Carboxylic Acid Succinimide." [PMID:20050626, PMID:23085224]
-synonym: "PCAS-H4" EXACT []
-synonym: "PCAS-d0" EXACT []
-synonym: "PCASS" EXACT []
-property_value: bridgeFormula: "C6 H3 N1 O1" xsd:string
-property_value: monoIsotopicMass: "105.02146" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-
-[Term]
-id: XLMOD:02052
-name: PCAS-d4
-def: "Pyridine-3-Carboxylic Acid Succinimide." [PMID:20050626, PMID:23085224]
-synonym: "PCASS-d4" EXACT []
-property_value: bridgeFormula: "C6 D3 N1 O1" xsd:string
-property_value: doubletDeltaMass: "4.02508" xsd:double
-property_value: monoIsotopicMass: "109.04812" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-
-[Term]
-id: XLMOD:02053
-name: DSA-13C6
-def: "13C labelled disuccinimidyladipic acid." [PSI:XL]
-property_value: bridgeFormula: "13C6 H6 O2" xsd:string
-property_value: doubletDeltaMass: "6.02016" xsd:double
-property_value: monoIsotopicMass: "116.0564" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_labelled XLMOD:00036 ! 13C labelled
-
-[Term]
-id: XLMOD:02054
-name: CBDPS-d8
-def: "Deuterium labelled cyanurbiotindipropionylsuccinimide." [PMID:20622150]
-property_value: bridgeFormula: "C19 D8 H15 N7 O4 S3" xsd:string
-property_value: doubletDeltaMass: "8.05016" xsd:double
-property_value: monoIsotopicMass: "517.14698" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "14.0" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00035 ! CID cleavable
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-
-[Term]
-id: XLMOD:02055
-name: CBDPSS
-def: "Cyanurbiotindimercaptopropionylsulfosuccinimide." [PMID:20622150]
-synonym: "Sulfo-CBDPSS" EXACT []
-property_value: bridgeFormula: "C19 H23 N7 O4 S3" xsd:string
-property_value: monoIsotopicMass: "509.09682" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "14.0" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: is_cleavable XLMOD:00035 ! CID cleavable
-
-[Term]
-id: XLMOD:02056
-name: CBDPSS-d8
-def: "Deuterium labelled cyanurbiotindimercaptopropionylsulfosuccinimide." [PMID:20622150]
-property_value: bridgeFormula: "C19 D8 H15 N7 O4 S3" xsd:string
-property_value: doubletDeltaMass: "8.05016" xsd:double
-property_value: monoIsotopicMass: "517.14698" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "14.0" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: is_cleavable XLMOD:00035 ! CID cleavable
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-
-[Term]
-id: XLMOD:02057
-name: SDH
-def: "Suberic acid 1,8-dihydrazide." [CAS:20247-84-1, PMID:24938783, ChemSpiderID:520361, ChemicalBookNo:CB8664268]
-property_value: bridgeFormula: "C8 H14 N4" xsd:string
-property_value: monoIsotopicMass: "166.12184649" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00110 ! hydrazide
-
-[Term]
-id: XLMOD:02058
-name: SDH-d12
-def: "Deuterium labelled suberic acid 1,8-dihydrazide." [PMID:24938783]
-property_value: bridgeFormula: "C8 D12 H2 N4" xsd:string
-property_value: doubletDeltaMass: "12.07573" xsd:double
-property_value: monoIsotopicMass: "178.1971667418" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00110 ! hydrazide
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-
-[Term]
-id: XLMOD:02059
-name: ADH
-def: "Adipic acid 1,6-dihydrazide." [CAS:1071-93-8, ChemSpiderID:59505, ChemicalBookNo:CB4129556, PMID:24938783]
-property_value: bridgeFormula: "C6 H10 N4" xsd:string
-property_value: monoIsotopicMass: "138.09054635" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00110 ! hydrazide
-
-[Term]
-id: XLMOD:02060
-name: ADH-d8
-def: "Deuterium labelled adipic acid 1,6-dihydrazide." [PMID:24938783]
-property_value: bridgeFormula: "C6 D8 H2 N4" xsd:string
-property_value: doubletDeltaMass: "8.05016" xsd:double
-property_value: monoIsotopicMass: "146.140760302" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00110 ! hydrazide
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-
-[Term]
-id: XLMOD:02061
-name: GDH
-def: "Glutaric acid 1,5-dihydrazide." [CAS:1508-67-4, ChemSpiderID:3179469, ChemicalBookNo:CB4453510, PMID:24938783]
-property_value: bridgeFormula: "C5 H8 N4" xsd:string
-property_value: monoIsotopicMass: "124.07489628" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00110 ! hydrazide
-
-[Term]
-id: XLMOD:02062
-name: GDH-d6
-def: "Deuterium labelled glutaric acid 1,5-dihydrazide." [PMID:24938783]
-property_value: bridgeFormula: "C5 D6 H2 N4" xsd:string
-property_value: doubletDeltaMass: "6.04368" xsd:double
-property_value: monoIsotopicMass: "130.112556744" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00110 ! hydrazide
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-
-[Term]
-id: XLMOD:02063
-name: BS3-d12
-def: "Deuterium labelled (bis(sulfosuccinimidyl) 2,2,3,3,4,4,5,5,6,6,7,7-suberate)." [PSI:XL]
-property_value: doubletDeltaMass: "12.07573" xsd:double
-property_value: monoIsotopicMass: "150.14381" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "11.4" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-
-[Term]
-id: XLMOD:02064
-name: DSG-d6
-def: "Deuterium labelled disuccinimidyl 2,2,3,3,4,4-glutarate." [PSI:XL]
-property_value: bridgeFormula: "C5 D6 O2" xsd:string
-property_value: doubletDeltaMass: "6.02016" xsd:double
-property_value: monoIsotopicMass: "102.05821" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "7.7" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-
-[Term]
-id: XLMOD:02065
-name: BS2G-d6
-def: "Deuterium labelled bis(sulfosuccinimidyl) 2,2,3,3,4,4-glutarate." [PSI:XL]
-synonym: "DSSG-d6" EXACT []
-property_value: bridgeFormula: "C5 D4 O2" xsd:string
-property_value: doubletDeltaMass: "4.02508" xsd:double
-property_value: monoIsotopicMass: "100.046236376" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "7.7" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-
-[Term]
-id: XLMOD:02066
-name: SATA
-def: "Succinimidyl acetylthioacetate." [CAS:76931-93-6, PubChem_Compound:127532, ChemSpiderID:113145, ChemicalBookNo:CB6378192]
-synonym: "N-succinimidyl S-acetylthioacetate" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "2.8" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-relationship: has_reactive_group XLMOD:00144 ! S-acetyl
-relationship: is_cleavable XLMOD:00025 ! hydroxylamine cleavable
-
-[Term]
-id: XLMOD:02067
-name: SATP
-def: "N-succinimidyl-S-acetylthiopropionate." [CAS:84271-78-3, PubChem_Compound:4110341, ChemSpiderID:3324023, ChemicalBookNo:CB7151156]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "4.1" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-relationship: has_reactive_group XLMOD:00144 ! S-acetyl
-relationship: is_cleavable XLMOD:00025 ! hydroxylamine cleavable
-
-[Term]
-id: XLMOD:02068
-name: LC-SMCC
-def: "Succinimidyl 4-(N-maleimidomethyl)cyclohexane-1-carboxy-(6-amidocaproate)." [CAS:125559-00-4, PubChem_Compound:3564731, ChemSpiderID:2802130, ChemicalBookNo:CB2681973]
-synonym: "Long chain-SMCC" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "16.2" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:02069
-name: PEAS
-def: "N-((2-pyridyldithio)ethyl)-4-azidosalicylamide." [MDL:MFCD00467787, PMID:11320237]
-synonym: "AES" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00109 ! pyridinyldisulfide
-relationship: has_reactive_group XLMOD:00114 ! aryl azide
-
-[Term]
-id: XLMOD:02070
-name: BisEA
-def: "Bis-(2-(Methanethiosulfonato)ethyl)amine." [PSI:XL]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00121 ! methanethiosulfonate
-
-[Term]
-id: XLMOD:02071
-name: 3,6,9,12-Tetraoxatetradecane-1,14-diyl dimethanethiosulfonate
-def: "3,6,9,12-Tetraoxatetradecane-1,14-diyl dimethanethiosulfonate cross-linker." [CAS:212262-08-3, PubChem_Compound:46783053, ChemSpiderID:3765062, ChemicalBookNo:CB4773508]
-synonym: "3,6,9,12-Tetraoxatetradecane-1,14-diyl-bis-methanethiosulfonate" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00121 ! methanethiosulfonate
-
-[Term]
-id: XLMOD:02072
-name: 3,6,9-Trioxaundecane-1,11-diyl dimethanethiosulfonate
-def: "3,6,9-Trioxaundecane-1,11-diyl dimethanethiosulfonate cross-linker." [CAS:212262-02-7, PubChem_Compound:5047788, ChemSpiderID:57565984, ChemicalBookNo:CB41175710]
-synonym: "3,6,9-Trioxaundecane-1,11-diyl-bismethanethiosulfonate" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00121 ! methanethiosulfonate
-
-[Term]
-id: XLMOD:02073
-name: MTS-1-MTS
-def: "1,1-Methanediyl Bismethanethiosulfonate." [CAS:22418-52-6, PubChem_Compound:4251850, ChemSpiderID:3459853, ChemicalBookNo:CB01175439]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00121 ! methanethiosulfonate
-
-[Term]
-id: XLMOD:02074
-name: MTS-2-MTS
-def: "1,2-Ethanediyl Bismethanethiosulfonate." [CAS:55-95-8, PubChem_Compound:564320, MDL:MFCD01320400, ChemSpiderID:490602, ChemicalBookNo:CB31175450]
-synonym: "1,2-Ethanedithiol Dimethanesulfonate" EXACT []
-synonym: "Preparation 289" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00121 ! methanethiosulfonate
-
-[Term]
-id: XLMOD:02075
-name: MTS-6-NHS
-def: "N-Succinimidyloxycarbonylpentyl methanethiosulfonate." [CAS:76078-81-4, PubChem_Compound:3614736, ChemSpiderID:2849984, ChemicalBookNo:CB6747738]
-synonym: "6-[(Methanethisulfonyl)thio]hexanoic acid, N-succinimidyl ester" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00121 ! methanethiosulfonate
-
-[Term]
-id: XLMOD:02076
-name: MTS-8-O2-MTS
-def: "3,6-dioxaoctane-1,8-diyl dimethanethiosulfonate." [CAS:212262-04-9, PubChem_Compound:3332000, ChemSpiderID:2579076, ChemicalBookNo:CB01175712]
-synonym: "1,2-bis(2-methylsulfonylsulfanylethoxy)ethane" EXACT []
-synonym: "3,6-Dioxaoctane-1,8-diyl Bismethanethiosulfonate" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00121 ! methanethiosulfonate
-
-[Term]
-id: XLMOD:02077
-name: MTS-11-MTS
-def: "Undecane-1,11-diyl-bismethanethiosulfonate." [PSI:XL]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00121 ! methanethiosulfonate
-
-[Term]
-id: XLMOD:02078
-name: BSOCOES
-def: "Bis(2-[Succinimidooxycarbonyloxy]ethyl) sulfone." [CAS:57683-72-4, PubChem_Compound:93771, ChemSpiderID:84638, ChemicalBookNo:CB6488705]
-property_value: bridgeFormula: "C6 H6 O6 S1" xsd:string
-property_value: monoIsotopicMass: "205.988512" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "13.0" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00061 ! base cleavable
-
-[Term]
-id: XLMOD:02079
-name: DPDPB
-def: "1,4-Di-(3'-[2'pyridyldithio]-propionamido) butane." [CAS:141647-62-3, PubChem_Compound:4187644, MDL:MFCD00153604, ChemSpiderID:3398412, ChemicalBookNo:CB1775965]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "19.9" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00109 ! pyridinyldisulfide
-
-[Term]
-id: XLMOD:02080
-name: Sulfo-DST
-def: "Sulfodisuccinimidyl tartrate." [CAS:118674-04-7, PubChem_Compound:3081171, ChemSpiderID:2338831, ChemicalBookNo:CB2297174]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "6.4" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: is_cleavable XLMOD:00024 ! periodate cleavable
-
-[Term]
-id: XLMOD:02081
-name: Sulfo-GMBS
-def: "N-gamma-Maleimidobutyryloxysulfosuccinimide ester." [CAS:185332-92-7, PubChem_Compound:23683309, ChemSpiderID:2678121, ChemicalBookNo:CB4412935]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "6.8" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:02082
-name: EMCH
-def: "N-(epsilon-Maleimidocaproic acid) hydrazide." [CAS:81186-33-6, PubChem_Compound:4170354, ChemSpiderID:3381797, ChemicalBookNo:CB1298684]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "11.8" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-relationship: has_reactive_group XLMOD:00110 ! hydrazide
-
-[Term]
-id: XLMOD:02083
-name: EMCH-TFA
-def: "N-(epsilon-Maleimidocaproic acid)hydrazide, TriFluoroacetic Acid." [CAS:151038-94-7, PubChem_Compound:23509306, ChemSpiderID:11567960, ChemicalBookNo:CB8349886]
-synonym: "2,5-Dihydro-2,5-dioxo-1H-pyrrole-1-hexanoic Acid Hydrazide 2,2,2-Trifluoroacetate" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "11.8" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00110 ! hydrazide
-
-[Term]
-id: XLMOD:02084
-name: Sulfo-EMCS
-def: "N-(epsilon-Maleimidocaproyloxy) sulfo succinimide ester." [CAS:215312-86-0, PubChem_Compound:4229287, ChemSpiderID:3438266, ChemicalBookNo:CB6793735]
-synonym: "6-Maleimidocaproic Acid Sulfo-N-Succinimidyl Ester" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "9.4" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:02085
-name: PMPI
-def: "N-(Maleimidophenyl) isocyanate." [CAS:123457-83-0, PubChem_Compound:129975, ChemSpiderID:115040, ChemicalBookNo:CB7497652]
-synonym: "N-(4-Isocyanatophenyl)maleimide" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "8.7" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-relationship: has_reactive_group XLMOD:00124 ! isocyanate
-
-[Term]
-id: XLMOD:02086
-name: SIAB
-def: "N-Succinimidyl(4-iodoacetyl)aminobenzoate." [CAS:72252-96-1, PubChem_Compound:126367, ChemSpiderID:112308, ChemicalBookNo:CB4386384]
-synonym: "4-[(2-Iodoacetyl)amino]benzoic Acid 2,5-dioxo-1-pyrrolidinyl Ester" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "10.6" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00127 ! iodoacetyl
-
-[Term]
-id: XLMOD:02087
-name: Sulfo-SIAB
-def: "N-Sulfosuccinimidyl(4-iodoacetyl)aminobenzoate." [CAS:144650-93-1, PubChem_Compound:4131104, ChemSpiderID:3343983, ChemicalBookNo:CB3328358]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "10.6" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: has_reactive_group XLMOD:00127 ! iodoacetyl
-
-[Term]
-id: XLMOD:02088
-name: Sulfo-SMPB
-def: "Sulfo succinimidyl 4-(maleimidophenyl) butyrate." [CAS:92921-26-1, PubChem_Compound:118855953, ChemSpiderID:32076952, ChemicalBookNo:CB5324783]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "11.6" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:02089
-name: MAL-PEG4-SCM
-def: "Succinimidyl-[(N-maleimidopropionamido)-tetraethyleneglycol] ester." [CAS:756525-99-2, PubChem_Compound:51340950, ChemSpiderID:32055651, ChemicalBookNo:CB22546917]
-synonym: "NHS-PEG4-Maleimide" EXACT []
-synonym: "Mal-PEG4-NHS-ester" EXACT []
-synonym: "Maleimide-PEG4-NHS" EXACT []
-synonym: "Malamido-PEG4-NHS" EXACT []
-synonym: "SM[PEG]4" EXACT []
-synonym: "O-[N-(3-Maleimidopropionyl)aminoethyl]-O'-[3-(N-succinimidyloxy)-3-oxopropyl]triethylene glycol" EXACT []
-synonym: "Succinimidyl-[(N-maleimidopropionamido)-dodecaethyleneglycol] ester" EXACT []
-property_value: hydrophilicPEGchain: "4" xsd:nonNegativeInteger
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "24.6" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:02090
-name: ABH
-def: "Azidobenzoyl hydrazide." [CAS:63296-32-2, PubChem_Compound:9812912, ChemSpiderID:7988662, ChemicalBookNo:CB0135326]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "11.9" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00110 ! hydrazide
-relationship: has_reactive_group XLMOD:00126 ! phenyl azide
-
-[Term]
-id: XLMOD:02091
-name: APG
-def: "p-Azidophenyl glyoxal monohydrate." [CAS:1196151-49-1, MDL:MFCD00150595, ChemSpiderID:11564450, ChemicalBookNo:CB3774159]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "9.3" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00126 ! phenyl azide
-relationship: has_reactive_group XLMOD:00142 ! phenylglyoxal
-
-[Term]
-id: XLMOD:02092
-name: APDP
-def: "4-Azido-2-hydroxy-N-(4-{[3-(2-pyridinyldisulfanyl)propanoyl]amino}butyl)benzamide." [ChemSpiderID:8496824, ChemicalBookNo:CB7382675]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "21.0" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_property XLMOD:00020 ! iodinatable
-relationship: has_reactive_group XLMOD:00109 ! pyridinyldisulfide
-relationship: has_reactive_group XLMOD:00125 ! hydroxyphenyl azide
-relationship: is_cleavable XLMOD:00023 ! cleavable S-S bond
-
-[Term]
-id: XLMOD:02093
-name: BASED
-def: "Bis(beta-[4-azidosalicylamido]-ethyl) disulfide." [CAS:199804-21-2, PubChem_Compound:3658531, ChemSpiderID:2891936, ChemicalBookNo:CB3363805]
-synonym: "Bis(2-(4-azidosalicylamido)ethyl) disulfide" EXACT []
-synonym: "N, N'-(Dithiobis-ethylene)bis(4-azido-2-hydroxy-benzamide)" EXACT []
-synonym: "N,N'-Bis(4-azidosalicoyl)cystamine" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "21.3" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_property XLMOD:00020 ! iodinatable
-relationship: has_reactive_group XLMOD:00125 ! hydroxyphenyl azide
-relationship: is_cleavable XLMOD:00023 ! cleavable S-S bond
-
-[Term]
-id: XLMOD:02094
-name: NHS-ASA
-def: "N-Hydroxysuccinimidyl-4-azidosalicyclic acid." [CAS:96602-46-9, PubChem_Compound:3035647, ChemSpiderID:2299834, PMID:2358439, ChemicalBookNo:CB21334997]
-synonym: "1-[(4-Azido-2-hydroxybenzoyl)oxy]-2,5-pyrrolidinedione" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "8.0" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_property XLMOD:00020 ! iodinatable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00125 ! hydroxyphenyl azide
-
-[Term]
-id: XLMOD:02095
-name: Sulfo-HSAB
-def: "N-Hydroxysulfosuccinimidyl-4-azidobenzoate." [CAS:199804-22-3, PubChem_Compound:10290999, ChemSpiderID:8466468, ChemicalBookNo:CB5222018]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "9.0" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: has_reactive_group XLMOD:00126 ! phenyl azide
-
-[Term]
-id: XLMOD:02096
-name: Sulfo-SAED
-def: "Sulfosuccinimidyl 2-(7-amino-4-methylcoumarin-3-acetamido)ethyl-1,3-dithiopropionate." [PubChem_Compound:132249, ChemSpiderID:116802]
-synonym: "2-SAED" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "23.6" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00015 ! fluorescent
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: has_reactive_group XLMOD:00135 ! azido-methylcoumarin
-relationship: is_cleavable XLMOD:00023 ! cleavable S-S bond
-
-[Term]
-id: XLMOD:02097
-name: Sulfo-SAND
-def: "Sulfosuccinimidyl 2-(m-azido-o-nitrobenzamido)-ethyl-1,3'-dithiopropionate." [MDL:MFCD02091654]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "18.5" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: has_reactive_group XLMOD:00107 ! nitrophenyl azide 
-relationship: is_cleavable XLMOD:00023 ! cleavable S-S bond
-
-[Term]
-id: XLMOD:02098
-name: SANPAH
-def: "N-Succinimidyl 6-(4-azido-2-nitroanilino)hexanoate." [CAS:64309-05-3, PubChem_Compound:3035550, ChemSpiderID:2299761, ChemicalBookNo:CB2262231]
-synonym: "6-(4-Azido-2-nitrophenylamino)hexanoic acid N-hydroxysuccinimide ester" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "18.2" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00107 ! nitrophenyl azide 
-
-[Term]
-id: XLMOD:02099
-name: Sulfo-SADP
-def: "Sulfosuccinimidyl (4-azidophenyl)-1,3'-dithiopropionate." [CAS:102568-45-6, PubChem_Compound:128116, ChemSpiderID:113597, ChemicalBookNo:CB9210802]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "13.9" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: has_reactive_group XLMOD:00126 ! phenyl azide
-relationship: is_cleavable XLMOD:00023 ! cleavable S-S bond
-
-[Term]
-id: XLMOD:02100
-name: SASD
-def: "Succinimidyl-2-(azidosalicylamido)ethyl-1,3-dithiopropionate." [CAS:144650-95-3, PubChem_Compound:4071585, ChemSpiderID:3286667, ChemicalBookNo:CB9276943]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "18.9" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_property XLMOD:00020 ! iodinatable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00125 ! hydroxyphenyl azide
-relationship: is_cleavable XLMOD:00023 ! cleavable S-S bond
-
-[Term]
-id: XLMOD:02101
-name: Sulfo-SASD
-def: "Sulfosuccinimidyl-2-(azidosalicylamido)ethyl-1,3-dithiopropionate." [CAS:144650-95-3, PubChem_Compound:6098351, ChemSpiderID:3286667, ChemicalBookNo:CB9276943]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "18.9" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_property XLMOD:00020 ! iodinatable
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: has_reactive_group XLMOD:00125 ! hydroxyphenyl azide
-relationship: is_cleavable XLMOD:00023 ! cleavable S-S bond
-
-[Term]
-id: XLMOD:02102
-name: DTTDPS
-def: "DTTDPS cross-linker." [PMID:20109223]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00024 ! periodate cleavable
-
-[Term]
-id: XLMOD:02103
-name: 1,4-diacetalbenzene
-def: "1,4-diacetalbenzene reagent." [CAS:1074-12-0, PubChem_Compound:14090, ChemSpiderID:13470, ChemicalBookNo:CB3357077, PMID:18936057, PMID:16875836]
-synonym: "Phenyldiglyoxal" EXACT []
-synonym: "PDG" EXACT []
-property_value: monoIsotopicMass: "190.027" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "7.5" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00115 ! glyoxal
-
-[Term]
-id: XLMOD:02104
-name: DiBMADPS
-def: "Bis(2,5-dioxopyrrolidin-1-yl)3,3'-(3,5-dibromo-4-methylphenylazanediyl)diproponate." [https://getd.libs.uga.edu/pdfs/hoffman_lisabeth_l_201008_phd.pdf]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00035 ! CID cleavable
-relationship: is_labelled XLMOD:00044 ! mass defect labelled
-
-[Term]
-id: XLMOD:02105
-name: DiBBSIAS
-def: "Bis(2,5-dioxopyrrolidin-1-yl) 2,2'-(2,4-dibromophenylsulfonylazanediyl)diacetate." [https://getd.libs.uga.edu/pdfs/hoffman_lisabeth_l_201008_phd.pdf]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00035 ! CID cleavable
-relationship: is_labelled XLMOD:00044 ! mass defect labelled
-
-[Term]
-id: XLMOD:02106
-name: BID
-def: "N-benzyliminodiacetoyloxysuccinimid." [PMID:11212007]
-property_value: CID_Fragment: "91" xsd:double
-property_value: CID_Fragment: "275.1" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00035 ! CID cleavable
-
-[Term]
-id: XLMOD:02107
-name: BCCL1
-def: "Bis-(N-hydroxysuccinimidyl) 3-amino-N-biotinoyl-1,5-pentanedioate." [PMID:19412923]
-property_value: monoIsotopicMass: "337.10962" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-
-[Term]
-id: XLMOD:02108
-name: BCCL2
-def: "Bis-(N-hydroxysuccinimidyl) 5-amino-N-biotinoyl-1,9-nonanedioate." [PMID:19412923]
-property_value: monoIsotopicMass: "393.17222" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-
-[Term]
-id: XLMOD:02109
-name: SBC
-def: "N-succinimidyl p-benzoyldihydrocinnamate." [PMID:19653199, ChemSpiderID:4488161]
-property_value: monoIsotopicMass: "236.09" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00119 ! benzophenone
-
-[Term]
-id: XLMOD:02110
-name: SBDC
-def: "Deuterium labelled N-succinimidyl p-benzoyldihydrocinnamate." [PMID:19653199]
-synonym: "SBC-d2" EXACT []
-property_value: doubletDeltaMass: "2.01254" xsd:double
-property_value: monoIsotopicMass: "238.10" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00119 ! benzophenone
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-
-[Term]
-id: XLMOD:02111
-name: S-Methyl 5,5'-thiodipentanoylhydroxysuccinimidemethylsulfate
-def: "S-Methyl 5,5'-thiodipentanoylhydroxysuccinimidemethylsulfate cross-linker." [PMID:19551991]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00035 ! CID cleavable
-
-[Term]
-id: XLMOD:02112
-name: SuDP
-def: "Bisuccinimidyl-succinamyl-aspartyl-proline." [PMID:26091612, PMID:20560670, PMID:17134140]
-synonym: "Disuccinimidyl-succinamyl-aspartyl-proline" EXACT []
-property_value: CID_Fragment: "97.0528" xsd:double
-property_value: CID_Fragment: "197.0324" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "11.2" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00035 ! CID cleavable
-
-[Term]
-id: XLMOD:02113
-name: SuDPG
-def: "Bisuccinimidyl-succinamyl-aspartyl-prolyl-glycine." [PMID:26091612, PMID:17134140]
-synonym: "Disuccinimidyl-succinamyl-aspartyl-prolyl-glycine" EXACT []
-property_value: CID_Fragment: "97.1" xsd:double
-property_value: CID_Fragment: "154.1" xsd:double
-property_value: CID_Fragment: "197.1" xsd:double
-property_value: CID_Fragment: "215.1" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "15.1" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00035 ! CID cleavable
-
-[Term]
-id: XLMOD:02114
-name: IRCX
-def: "Dibenzoyloxysuccinimidylethyl phosphate." [PMID:18517224]
-comment: An IR chromogenic crosslinker.
-property_value: monoIsotopicMass: "330.0" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "16" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-
-[Term]
-id: XLMOD:02115
-name: BAMG
-def: "Bis(succinimidyl)-3-azidomethyl glutarate." [PMID:17600791]
-property_value: monoIsotopicMass: "125.048" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "7.5" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00042 ! TCEP cleavable
-
-[Term]
-id: XLMOD:02116
-name: azide-DSG
-def: "Bis(succinimidyl)-3-azidomethyl glutarate." [PMID:20472459]
-property_value: monoIsotopicMass: "211.0" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "7.7" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_handle XLMOD:00055 ! azide
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-
-[Term]
-id: XLMOD:02117
-name: 1
-def: "Crosslinking reagent 1." [PMID:14698174]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "8.7" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-
-[Term]
-id: XLMOD:02118
-name: JMV 3378
-def: "Crosslinking reagent JMV 3378." [PMID:19902427]
-property_value: monoIsotopicMass: "268.0" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_handle XLMOD:00056 ! CHCA
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-
-[Term]
-id: XLMOD:02119
-name: BuTuGPG
-def: "4-[3-(2-{2-[(2,5-dioxo-pyrrolidin-1-yloxycarbonyl-methyl)-carbamoyl]-pyrrolidin-1-yl}-2-oxo-ethyl)-thioureido]-butyric acid 2,5-dioxo-pyrrolidin-1-yl ester." [PMID:19950134]
-synonym: "NHS-butyric acid-thiourea-glycine-proline-glycine-NHS" EXACT []
-synonym: "NHS-BuTuGPG-NHS" EXACT []
-synonym: "Edman linker" EXACT []
-property_value: monoIsotopicMass: "1686.84" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "16.7" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00035 ! CID cleavable
-
-[Term]
-id: XLMOD:02120
-name: BuUrBu
-def: "NHS-amino butyric acid-urea-amino butyric acid-NHS." [CAS:1240387-33-0, PubChem_Compound:86106597, ChemSpiderID:65999926, PMID:30074391, PMID:21157862, PMID:20704385, PMID:25261217, PMID:27428000]
-synonym: "NHS-BuUrBu-NHS" EXACT []
-synonym: "Disuccinimidyl dibutyric urea" EXACT []
-synonym: "DSBU" EXACT []
-property_value: CID_Fragment: "85.053" xsd:double
-property_value: CID_Fragment: "111.032" xsd:double
-property_value: doubletDeltaMass: "25.979" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "12.5" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_neutral_loss_reporter XLMOD:00057 ! generic neutral loss reporter
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00035 ! CID cleavable
-
-[Term]
-id: XLMOD:02121
-name: DPS
-def: "Diphtalimide suberate." [PMID:19994840]
-comment: Contains an eight-carbon spacer arm.
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00104 ! N-hydroxyphthalimide
-
-[Term]
-id: XLMOD:02122
-name: SBBT
-def: "1,1'-(suberoyldioxy)bisbenzotriazole." [PMID:19994840]
-comment: Contains an eight-carbon spacer arm.
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00129 ! hydroxybenzotriazole
-
-[Term]
-id: XLMOD:02123
-name: SBAT
-def: "1,1'-(suberoyldioxy)bisazabenzotriazole." [PMID:19994840]
-comment: Contains an eight-carbon spacer arm.
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00130 ! 1-hydroxy-7-azabenzotriazole
-
-[Term]
-id: XLMOD:02124
-name: SDAD
-def: "Succinimidyl 2-([4,4'-azipentanamido]ethyl)-1,3'-dithiopropionate." [PMID:20635431, PMID:25251153]
-synonym: "NHS-SS-Diazirine" EXACT []
-property_value: monoIsotopicMass: "273.0" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "13.5" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_neutral_loss_reporter XLMOD:00057 ! generic neutral loss reporter
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00103 ! diazirine
-relationship: is_cleavable XLMOD:00023 ! cleavable S-S bond
-
-[Term]
-id: XLMOD:02125
-name: Sulfo-SDAD
-def: "Sulfosuccinimidyl 2-([4,4'-azipentanamido]ethyl)-1,3'-dithiopropionate." [CAS:1226983-32-9, PubChem_Compound:124202976]
-synonym: "Sulfo-NHS-SS-Diazirine" EXACT []
-property_value: monoIsotopicMass: "273.0" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "13.5" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_neutral_loss_reporter XLMOD:00057 ! generic neutral loss reporter
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: has_reactive_group XLMOD:00103 ! diazirine
-relationship: is_cleavable XLMOD:00023 ! cleavable S-S bond
-
-[Term]
-id: XLMOD:02126
-name: DSSO
-def: "Disuccinimidyl sulfoxide." [PubChem_Compound:86106597, ChemSpiderID:65999926, PMID:20736410, PMID:27417384]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "10.1" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00067 ! CID cleavable C-S bond
-
-[Term]
-id: XLMOD:02127
-name: DEST
-def: "Diethylsuberthioimidate." [PubChem_Compound:88869905, ChemSpiderID:67491002, PMID:20795639, PMID:22460622]
-property_value: bridgeFormula: "C8 H12 N2" xsd:string
-property_value: monoIsotopicMass: "136.10004842" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "11.0" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00131 ! thioimidate
-relationship: is_cleavable XLMOD:00035 ! CID cleavable
-
-[Term]
-id: XLMOD:02128
-name: cis-Diamminedichloroplatinum (II)
-def: "Cis-[Pt(NH3)2Cl2]." [CAS:15663-27-1, PubChem_Compound:441203, ChemSpiderID:76401, ChemicalBookNo:CB9236183, PMID:21591778, PMID:16875836]
-synonym: "Cis-platin" EXACT []
-synonym: "CPT" EXACT []
-property_value: monoIsotopicMass: "225.995" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "4.63" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00132 ! platinum(II)
-
-[Term]
-id: XLMOD:02129
-name: DC4
-def: "DC4 cross-linker containing a DABCO (1,4-diazabicyclo[2.2.2]octane) moiety." [CAS:1374647-94-5, ChemSpiderID:29763722, ChemicalBookNo:CB63152601, PMID:22131227]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "18.0" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00018 ! cleavable by MS2 labile bond
-relationship: is_cleavable XLMOD:00035 ! CID cleavable
-relationship: is_cleavable XLMOD:00040 ! ISD cleavable
-
-[Term]
-id: XLMOD:02130
-name: ASBA
-def: "4-(p-Azidosalicylamido)butylamine." [MDL:MFCD00153599, ChemSpiderID:8013538, ChemicalBookNo:CB0295398]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "16.3" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_property XLMOD:00020 ! iodinatable
-relationship: has_reactive_group XLMOD:00125 ! hydroxyphenyl azide
-relationship: has_reactive_group XLMOD:00133 ! amine reactive group
-
-[Term]
-id: XLMOD:02131
-name: SPB
-def: "Succinimidyl-[4-(psoralen-8-yloxy)]-butyrate." [CAS:129211-47-8, PubChem_Compound:15950836, MDL:MFCD01868521, ChemicalBookNo:CB5449965]
-synonym: "NHS-Psoralen" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "8.6" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00134 ! psoralen
-
-[Term]
-id: XLMOD:02132
-name: Sulfo-NHS-LC-ASA
-def: "Sulfosuccinimidyl(4-azido-salicylamido) hexanoate." [CAS:184533-12-8, PubChem_Compound:10162222, ChemSpiderID:8337730, ChemicalBookNo:CB8475750]
-synonym: "Sulfo-NHS-Long Chain-ASA" EXACT []
-synonym: "SAH" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "18.0" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00020 ! iodinatable
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: has_reactive_group XLMOD:00125 ! hydroxyphenyl azide
-
-[Term]
-id: XLMOD:02133
-name: Sulfo-SFAD
-def: "Sulfosuccinimidyl(perfluoroazidobenzamido)ethyl-1,3´-dithiopropionate." [CAS:220446-74-2, PubChem_Compound:90471066, ChemSpiderID:30798432, ChemicalBookNo:CB9178443]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "14.6" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: has_reactive_group XLMOD:00136 ! perfluoroaryl azide
-relationship: is_cleavable XLMOD:00023 ! cleavable S-S bond
-
-[Term]
-id: XLMOD:02134
-name: SDA
-def: "Succinimidyl-ester diazirine." [PubChem_Compound:89937136, MDL:MFCD28899672]
-synonym: "NHS-Diazirine" EXACT []
-property_value: bridgeFormula: "C5 H6 O1" xsd:string
-property_value: monoIsotopicMass: "82.04186484" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "3.9" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00103 ! diazirine
-
-[Term]
-id: XLMOD:02135
-name: LC-SDA
-def: "NHS-LC-Diazirine." [PSI:XL]
-synonym: "NHS-LC-Diazirine" EXACT []
-synonym: "Long Chain-SDA" EXACT []
-synonym: "Succinimidyl 6-(4,4'-azipentanamido)hexanoate" EXACT []
-property_value: bridgeFormula: "C11 H12 N1 O2" xsd:string
-property_value: monoIsotopicMass: "195.125928855" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "12.5" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00103 ! diazirine
-
-[Term]
-id: XLMOD:02136
-name: Sulfo-SDA
-def: "Sulfo-NHS-Diazirine." [PubChem_Compound:121371016, PMID:28430416]
-synonym: "Sulfosuccinimidyl 4,4'-azipentanoate" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "3.9" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: has_reactive_group XLMOD:00103 ! diazirine
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-
-[Term]
-id: XLMOD:02137
-name: Sulfo-LC-SDA
-def: "Sulfo-NHS-LC-Diazirine." [CAS:1909307-62-5, PubChem_Compound:124202974, MDL:MFCD28899432]
-synonym: "Sulfosuccinimidyl 6-(4,4'-azipentanamido)hexanoate" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "12.5" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: has_reactive_group XLMOD:00103 ! diazirine
-
-[Term]
-id: XLMOD:02138
-name: DMA
-def: "Dimethyl adipimidate dihydrochloride." [CAS:14620-72-5, PubChem_Compound:25738, ChemSpiderID:34991296, ChemicalBookNo:CB4714688]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "8.6" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00111 ! imidoester
-
-[Term]
-id: XLMOD:02139
-name: DMP
-def: "Dimethyl pimelimidate dihydrochloride." [CAS:58537-94-3, PubChem_Compound:11402688, ChemSpiderID:10637821, ChemicalBookNo:CB7380424]
-synonym: "Dimethyl pimelinediimidate dihydrochloride" EXACT []
-property_value: bridgeFormula: "C7 H10 N2" xsd:string
-property_value: monoIsotopicMass: "122.08439835" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "9.2" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00111 ! imidoester
-
-[Term]
-id: XLMOD:02140
-name: DMS
-def: "Dimethyl suberimidate dihydrochloride." [CAS:34490-86-3, PubChem_Compound:118696, ChemicalBookNo:CB9142806]
-synonym: "Dimethyl ester octanediimidic acid dihydrochloride" EXACT []
-synonym: "1,8-Dimethoxyoctane-1,8-diyldiammonium dichloride" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "11.0" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00111 ! imidoester
-
-[Term]
-id: XLMOD:02141
-name: DTBP
-def: "Dimethyl 3,3'-dithiobispropionimidate dihydrochloride." [CAS:38285-78-8, PubChem_Compound:123988, ChemSpiderID:10628577, ChemicalBookNo:CB5208751]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "11.9" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00111 ! imidoester
-relationship: is_cleavable XLMOD:00023 ! cleavable S-S bond
-
-[Term]
-id: XLMOD:02142
-name: Sulfo-BSOCOES
-def: "Bis(2-[Sulfosuccinimidooxycarbonyloxy]ethyl) sulfone." [CAS:161011-72-9, PubChem_Compound:10232304, ChemicalBookNo:CB62131214, PMID:7356718]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "13.0" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: is_cleavable XLMOD:00061 ! base cleavable
-
-[Term]
-id: XLMOD:02143
-name: BMH
-def: "1,6-Bis-maleimidohexane." [CAS:4856-87-5, PubChem_Compound:20992, ChemSpiderID:19746, ChemicalBookNo:CB9745265]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "16.1" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:02144
-name: DFDNB
-def: "1-5-Difluoro-2,4-dinitrobenzene." [CAS:327-92-4, PubChem_Compound:67598, ChemSpiderID:60919, ChemicalBookNo:CB2488813]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "3.0" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-is_a: XLMOD:09243 ! Sanger type reagent
-relationship: has_reactive_group XLMOD:00145 ! aryl halide
-
-[Term]
-id: XLMOD:02145
-name: SMPT
-def: "4-Succinimidyloxycarbonyl-methyl-alpha-(2-pyridyldithio)toluene." [CAS:112241-19-7, PubChem_Compound:130706, MDL:MFCD00083161, ChemSpiderID:115608, ChemicalBookNo:CB5359464]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "11.2" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00109 ! pyridinyldisulfide
-
-[Term]
-id: XLMOD:02146
-name: SDBP
-def: "N-hydroxysuccinimidyl-2-3-dibromopropionate." [CAS:118790-78-6, PubChem_Compound:195278, ChemSpiderID:169350, ChemicalBookNo:CB61318997]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00128 ! bromoacetyl
-
-[Term]
-id: XLMOD:02147
-name: HSAB
-def: "N-hydroxysuccinimidyl 4-azidobenzoate." [CAS:53053-08-0, PubChem_Compound:122153, MDL:MFCD00054963, ChemSpiderID:108951, ChemicalBookNo:CB5187007]
-synonym: "4-Azidobenzoyloxysuccinimide" EXACT []
-synonym: "2,5-dioxopyrrolidin-1-yl) 4-azidobenzoate" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "9.0" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00126 ! phenyl azide
-
-[Term]
-id: XLMOD:02148
-name: ASIB
-def: "1-(p-azidosalicylamido)-4-(iodoacetamido)butane." [PubChem_Compound:10002006, ChemSpiderID:8177587, ChemicalBookNo:CB3741230]
-synonym: "1-(4-Azidosalicylamido)-4-(iodoacetamido)butane" EXACT []
-synonym: "4-Azido-2-hydroxy-N-{4-[(iodoacetyl)amino]butyl}benzamide" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "18.8" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00126 ! phenyl azide
-relationship: has_reactive_group XLMOD:00127 ! iodoacetyl
-
-[Term]
-id: XLMOD:02149
-name: SAND
-def: "Succinimidyl-2-[m-azido-o-nitrobenzamido]ethyl-1,3'-dithiopropionate." [MDL:MFCD02091654]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "18.5" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00107 ! nitrophenyl azide
-relationship: is_cleavable XLMOD:00041 ! thiol cleavable
-
-[Term]
-id: XLMOD:02150
-name: SADP
-def: "N-Succinimidyl (4-azidophenyl) 1,3´-dithiopropionate." [CAS:74676-98-5, PubChem_Compound:494250, ChemSpiderID:432600, ChemicalBookNo:CB7748141]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "13.9" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00126 ! phenyl azide
-relationship: is_cleavable XLMOD:00023 ! cleavable S-S bond
-
-[Term]
-id: XLMOD:02151
-name: PNP-DTP
-def: "p-nitrophenyl-2-diazo-3,3,3-trifluoropropionate." [CAS:59733-94-7, PubChem_Compound:5748175, ChemSpiderID:11489106, ChemicalBookNo:CB41358102]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "10.0" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_property XLMOD:00020 ! iodinatable
-relationship: has_reactive_group XLMOD:00107 ! nitrophenyl azide
-relationship: has_reactive_group XLMOD:00137 ! diazo group
-
-[Term]
-id: XLMOD:02152
-name: SAED
-def: "Succinimidyl-2-(7-azido-4-methylcoumarin-3-acetamido)ethyl-1,3'-dithiopropionate." [CAS:139609-20-4,PubChem_Compound:90469951, ChemSpiderID:52563941, ChemicalBookNo:CB5455874, PMID:1597185]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "23.6" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00102 ! Sulfo-NHS ester
-relationship: has_reactive_group XLMOD:00135 ! azido-methylcoumarin
-relationship: is_cleavable XLMOD:00023 ! cleavable S-S bond
-
-[Term]
-id: XLMOD:02153
-name: Sulfo-SAMCA
-def: "Sulfosuccinimidyl-7-azido-4-methylcoumarin-3-acetate." [CAS:223572-57-4, PubChem_Compound:10137892, ChemSpiderID:8313404, ChemicalBookNo:CB02702784]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "12.8" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: has_reactive_group XLMOD:00135 ! azido-methylcoumarin
-
-[Term]
-id: XLMOD:02154
-name: MSA
-def: "Methyl N-succinimidyl adipate." [CAS:118380-06-6, PubChem_Compound:4458286, ChemSpiderID:3657094, ChemicalBookNo:CB3716645]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "7.2" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-
-[Term]
-id: XLMOD:02155
-name: Maleimide-PEG2-NHS
-def: "Succinimidyl-[(N-maleimidopropionamido)-diethyleneglycol] ester." [CAS:955094-26-5, PubChem_Compound:51340948, MDL:MFCD11041137, ChemSpiderID:32055652, ChemicalBookNo:CB22501435]
-synonym: "NHS-PEG2-Maleimide" EXACT []
-synonym: "Malamido-PEG2-NHS" EXACT []
-synonym: "Succinimide-Maleimide PEG" EXACT []
-synonym: "SM[PEG]2" EXACT []
-property_value: hydrophilicPEGchain: "2" xsd:nonNegativeInteger
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "17.6" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:02156
-name: Maleimide-PEG6-NHS
-def: "Succinimidyl-[(N-maleimidopropionamido)-hexaethyleneglycol] ester." [CAS:1137109-21-7, PubChem_Compound:77078209, MDL:MFCD11041093, ChemSpiderID:32055650, ChemicalBookNo:CB82546919]
-synonym: "NHS-PEG6-Maleimide" EXACT []
-synonym: "Malamido-PEG6-NHS" EXACT []
-synonym: "SM[PEG]6" EXACT []
-property_value: hydrophilicPEGchain: "6" xsd:nonNegativeInteger
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "32.5" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:02157
-name: Maleimide-PEG8-NHS
-def: "Succinimidyl-[(N-maleimidopropionamido)-octaethyleneglycol] ester." [CAS:756525-93-6, PubChem_Compound:57568672, MDL:MFCD11041144, ChemSpiderID:32055649, ChemicalBookNo:CB62546920]
-synonym: "NHS-PEG8-Maleimide" EXACT []
-synonym: "Malamido-PEG8-NHS" EXACT []
-synonym: "SM[PEG]8" EXACT []
-property_value: hydrophilicPEGchain: "8" xsd:nonNegativeInteger
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "39.25" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:02158
-name: Maleimide-PEG12-NHS
-def: "Succinimidyl-[(N-maleimidopropionamido)-dodecaethyleneglycol] ester." [CAS:1426151-00-9, PubChem_Compound:51340947, MDL:MFCD11041148, ChemSpiderID:32055629, ChemicalBookNo:CB32750847]
-synonym: "NHS-PEG12-Maleimide" EXACT []
-synonym: "Malamido-PEG12-NHS" EXACT []
-synonym: "SM[PEG]12" EXACT []
-property_value: hydrophilicPEGchain: "12" xsd:nonNegativeInteger
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "53.4" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:02159
-name: Maleimide-PEG24-NHS
-def: "Succinimidyl-[(N-maleimidopropionamido)-tetracosaethyleneglycol] ester." [PubChem_Compound:89408683]
-synonym: "NHS-PEG24-Maleimide" EXACT []
-synonym: "Malamido-PEG24-NHS" EXACT []
-synonym: "SM[PEG]24" EXACT []
-property_value: hydrophilicPEGchain: "24" xsd:nonNegativeInteger
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "95.2" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:02160
-name: 11-Maleimidoundecanoic Acid Sulfo-N-Succinimidyl Ester
-def: "11-Maleimidoundecanoic Acid Sulfo-N-Succinimidyl Ester cross-linker." [CAS:211236-68-9, PubChem_Compound:5066232, MDL:MFCD01075057, ChemSpiderID:4243138, ChemicalBookNo:CB51025445]
-synonym: "Sulfo-Kmus" EXACT []
-property_value: hydrophilicPEGchain: "4" xsd:nonNegativeInteger
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "15.7" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:02161
-name: DTME
-def: "Dithio-bis-maleimidoethane." [CAS:71865-37-7, PubChem_Compound:191989, MDL:MFCD01863385, ChemSpiderID:166677, ChemicalBookNo:CB3134825]
-synonym: "Dithio-bis-maleimidoethane" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "13.3" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-relationship: is_cleavable XLMOD:00023 ! cleavable S-S bond
-
-[Term]
-id: XLMOD:02162
-name: 3-N-Maleimidobenzoic Acid N-Succinimidyl Ester
-def: "3-N-Maleimidobenzoic Acid N-Succinimidyl Ester cross-linker." [CAS:58626-38-3, PubChem_Compound:93861, ChemSpiderID:84714, ChemicalBookNo:CB0342553]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "9.9" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:02163
-name: N-Succinimidyl 3-(Bromoacetamido)propionate
-def: "N-Succinimidyl 3-(Bromoacetamido)propionate cross-linker." [CAS:57159-62-3, PubChem_Compound:4463814, ChemSpiderID:3662399, ChemicalBookNo:CB1123003]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "6.2" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00128 ! bromoacetyl
-
-[Term]
-id: XLMOD:02164
-name: MTS-3-MTS
-def: "1,3-Propanediyl bismethanethiosulfonate." [CAS:55-96-9, PubChem_Compound:571841, ChemSpiderID:497206, ChemicalBookNo:CB51175454]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00121 ! methanethiosulfonate
-
-[Term]
-id: XLMOD:02165
-name: MTS-4-MTS
-def: "1,4-Butanediyl bismethanethiosulfonate." [CAS:55-99-2, PubChem_Compound:241169, ChemSpiderID:210759, ChemicalBookNo:CB11175456]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00121 ! methanethiosulfonate
-
-[Term]
-id: XLMOD:02166
-name: MTS-5-MTS
-def: "1,5-Pentanediyl bismethanethiosulfonate." [ChemSpiderID:58967]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00121 ! methanethiosulfonate
-
-[Term]
-id: XLMOD:02167
-name: MTS-6-MTS
-def: "1,6-Hexanediyl bismethanethiosulfonate." [CAS:56-01-9, PubChem_Compound:3360826, ChemSpiderID:2606746, ChemicalBookNo:CB61497498]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00121 ! methanethiosulfonate
-
-[Term]
-id: XLMOD:02168
-name: 6-maleimidocaproic acid
-def: "6-Maleimidocaproic acid cross-linker." [CAS:55750-53-3, PubChem_Compound:573683, MDL:MFCD00043140, ChemSpiderID:498795, ChemicalBookNo:CB6300928]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "9.4" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-relationship: has_reactive_group XLMOD:00138 ! carboxyl 
-
-[Term]
-id: XLMOD:02169
-name: SFAD
-def: "Succinimidyl(perfluoroazidobenzamido)ethyl-1,3´-dithiopropionate." [PubChem_Compound:90471066, ChemSpiderID:30798432, ChemicalBookNo:CB9178443]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "14.6" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00136 ! perfluoroaryl azide
-relationship: is_cleavable XLMOD:00023 ! cleavable S-S bond
-
-[Term]
-id: XLMOD:02170
-name: LCABH
-def: "LCABH cross-linker." [PSI:XL]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "14.6" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00110 ! hydrazide
-relationship: has_reactive_group XLMOD:00126 ! phenyl azide
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-
-[Term]
-id: XLMOD:02171
-name: NHS-LC-ASA
-def: "Succinimidyl(4-azido-salicylamido) hexanoate." [PSI:XL]
-synonym: "NHS-Long Chain-ASA" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "18.0" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00020 ! iodinatable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00125 ! hydroxyphenyl azide
-
-[Term]
-id: XLMOD:02172
-name: AEDP-HCl
-def: "3-([2-Aminoethyl] dithio)-propionic acid hydrochloride." [CAS:351422-31-6, ChemSpiderID:4366598, ChemicalBookNo:CB11564306]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "9.5" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00133 ! amine reactive group
-relationship: has_reactive_group XLMOD:00138 ! carboxyl
-relationship: is_cleavable XLMOD:00023 ! cleavable S-S bond
-
-[Term]
-id: XLMOD:02173
-name: AMAS
-def: "N-(alpha-Maleimidoacetoxy)-succinimide ester." [CAS:55750-61-3, PubChem_Compound:3299229, ChemSpiderID:2547634, ChemicalBookNo:CB4326351]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "4.4" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:02174
-name: BMB
-def: "1,4-Bis-Maleimidobutane." [CAS:28537-70-4, PubChem_Compound:239576, ChemSpiderID:209301, ChemicalBookNo:CB4131366]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "10.9" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:02175
-name: BMDB
-def: "1,4-Bis-Maleimidyl-2,3-dihydroxybutane." [ChemSpiderID:4222027, ChemicalBookNo:CB9370889]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "10.2" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-relationship: is_cleavable XLMOD:00024 ! periodate cleavable
-
-[Term]
-id: XLMOD:02176
-name: BMOE
-def: "Bis-Maleimidoethane." [CAS:5132-30-9, PubChem_Compound:237509, MDL:MFCD00458699, ChemSpiderID:11359915, ChemicalBookNo:CB5476024]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "8.0" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:02177
-name: BMPA
-def: "N-beta-Maleimidopropionic acid." [CAS:7423-55-4, PubChem_Compound:573621, ChemSpiderID:498738, ChemicalBookNo:CB1371466]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "5.9" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-relationship: has_reactive_group XLMOD:00138 ! carboxyl
-
-[Term]
-id: XLMOD:02178
-name: BMPH
-def: "N-(beta-Maleimidopropionic acid)hydrazide." [CAS:359436-60-5, PubChem_Compound:4401583, ChemSpiderID:3602748, ChemicalBookNo:CB0106874]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "8.1" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-relationship: has_reactive_group XLMOD:00110 ! hydrazide
-
-[Term]
-id: XLMOD:02179
-name: BM(PEG)2
-def: "1,8-Bis-Maleimidodiethyleneglycol." [CAS:115597-84-7, PubChem_Compound:3690297, MDL:MFCD01096749, ChemSpiderID:2922525, ChemicalBookNo:CB9190751]
-synonym: "BM[PEO]2" EXACT []
-synonym: "maleimide-PEG2-maleimide" EXACT []
-property_value: hydrophilicPEGchain: "2" xsd:nonNegativeInteger
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "14.7" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:02180
-name: BM(PEG)3
-def: "1,8-Bis-Maleimidotriethyleneglycol." [CAS:86099-06-1, PubChem_Compound:3331999, ChemSpiderID:2579075, ChemicalBookNo:CB9190751]
-synonym: "BM[PEO]3" EXACT []
-synonym: "maleimide-PEG3-maleimide" EXACT []
-property_value: hydrophilicPEGchain: "3" xsd:nonNegativeInteger
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "17.8" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:02181
-name: BM(PEG)4
-def: "1,11-Bis-Maleimidotetraethyleneglycol." [CAS:86099-06-1, PubChem_Compound:3331999, ChemSpiderID:2579075, ChemicalBookNo:CB8506674]
-synonym: "BM[PEO]4" EXACT []
-synonym: "maleimide-PEG4-maleimide" EXACT []
-property_value: hydrophilicPEGchain: "4" xsd:nonNegativeInteger
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "19.9" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:02182
-name: C6-SANH
-def: "C6-Succinimidyl 4-hydrazinonicotinate acetone hydrazone." [CAS:937249-76-8, ChemicalBookNo:CB9456561]
-comment: SANH with extended six carbon linker.
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "14.4" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00143 ! hydrazone
-
-[Term]
-id: XLMOD:02183
-name: C6-4-SFB
-def: "C6-Succinimidyl 4-formylbenzoate." [CAS:1005773-18-1, ChemicalBookNo:CB0456285]
-comment: SFB with extended six carbon linker.
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "13.5" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00141 ! carbonyl
-
-[Term]
-id: XLMOD:02184
-name: SBAP
-def: "Succinimdyl 3-(bromoacetamido)propionate." [CAS:57159-62-3, PubChem_Compound:4463814, ChemSpiderID:3662399, ChemicalBookNo:CB1123003]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "6.2" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00128 ! bromoacetyl
-
-[Term]
-id: XLMOD:02185
-name: SFB
-def: "Succinimidyl 4-formylbenzoate." [CAS:60444-78-2, PubChem_Compound:4126130, ChemSpiderID:3339198, ChemicalBookNo:CB7361809]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "5.8" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00141 ! carbonyl
-
-[Term]
-id: XLMOD:02186
-name: SHTH
-def: "Succinimidyl 4-hydrazidoterephthalate hydrochloride." [PSI:XL]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "7.9" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-relationship: has_reactive_group XLMOD:00110 ! hydrazide
-
-[Term]
-id: XLMOD:02187
-name: Sulfo-KMUS
-def: "N-(kappa-maleimidoundecanoyloxy)sulfosuccinimide ester." [CAS:220935-13-7, PubChem_Compound:5066232, ChemSpiderID:4243138, ChemicalBookNo:CB2774516]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "19.5" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:02188
-name: THPP
-def: "beta-(tris[hydroxymethyl]phosphine)propionic acid." [CAS:15931-64-3, PubChem_Compound:4095799, ChemSpiderID:3310006, ChemicalBookNo:CB2497718]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "3.03" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00138 ! carboxyl
-relationship: has_reactive_group XLMOD:00139 ! hydroxymethyl phosphine
-
-[Term]
-id: XLMOD:02189
-name: EMCA
-def: "N-epsilon-Maleimidocaproic acid." [CAS:55750-53-3, PubChem_Compound:573683, ChemSpiderID:2006116, ChemicalBookNo:CB6300928]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "9.4" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-relationship: has_reactive_group XLMOD:00138 ! carboxyl
-
-[Term]
-id: XLMOD:02190
-name: HBVS
-def: "1,6-Hexane-bis-vinylsulfone." [ChemicalBookNo:CB02711432, MDL:MFCD01866933]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "14.7" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00140 ! vinyl sulfone
-
-[Term]
-id: XLMOD:02191
-name: KMUA
-def: "N-kappa-Maleimidoundecanoic acid." [CAS:57079-01-3, PubChem_Compound:4618600, ChemSpiderID:3809539, ChemicalBookNo:CB41175477]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "15.7" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-relationship: has_reactive_group XLMOD:00138 ! carboxyl
-
-[Term]
-id: XLMOD:02192
-name: KMUH
-def: "N-(kappa-Maleimidoundecanoic acid)hydrazide." [CAS:359436-62-7, PubChem_Compound:4438236, ChemSpiderID:3637842, ChemicalBookNo:CB71175478]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "19.0" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-relationship: has_reactive_group XLMOD:00110 ! hydrazide
-relationship: is_cleavable XLMOD:00041 ! thiol cleavable
-
-[Term]
-id: XLMOD:02193
-name: MPBH
-def: "4-(4-N-Maleimidophenyl)butyric acid hydrazide-HCl." [PubChem_Compound:9904748, ChemSpiderID:8080402, ChemicalBookNo:CB0734136]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "17.9" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-relationship: has_reactive_group XLMOD:00110 ! hydrazide
-relationship: is_cleavable XLMOD:00041 ! thiol cleavable
-
-[Term]
-id: XLMOD:02194
-name: SANH
-def: "Succinimidyl-2-(m-azido-o-nitrobenzamido)ethyl 1,3'-dithiopropionate." [ChemSpiderID:32034301, ChemicalBookNo:CB8354354]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "6.7" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00143 ! hydrazone
-
-[Term]
-id: XLMOD:02195
-name: SAND-PR
-def: "Sulfosuccinimidyl-2-(m-azido-o-nitrobenzamido)ethyl 1,3'-dithiopropionate." [CAS:112820-42-5, MDL:MFCD02091654, ChemSpiderID:115619, ChemicalBookNo:CB71367710]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "6.7" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: has_reactive_group XLMOD:00143 ! hydrazone
-
-[Term]
-id: XLMOD:02196
-name: Sulfo-SAPD
-def: "Sulfosuccinimidyl 2-(4-azidosalicylamido) ethyl-1,3-dithioproprioonate." [ChemicalBookNo:CB5476059]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: has_reactive_group XLMOD:00125 ! hydroxyphenyl azide
-
-[Term]
-id: XLMOD:02197
-name: SAPD
-def: "Succinimidyl 2-(4-azidosalicylamido) ethyl-1,3-dithioproprioonate." [ChemicalBookNo:CB5476059]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00125 ! hydroxyphenyl azide
-
-[Term]
-id: XLMOD:02198
-name: BS(PEG)5
-def: "Bis(sulfosuccinimidyl)suberate pentaethyleneglycol." [CAS:756526-03-1, PubChem_Compound:51340935, ChemSpiderID:28604877, ChemicalBookNo:CB12663893]
-synonym: "NHS-PEG5-NHS" EXACT []
-property_value: bridgeFormula: "C14 H22 O7" xsd:string
-property_value: hydrophilicPEGchain: "5" xsd:nonNegativeInteger
-property_value: monoIsotopicMass: "302.13655" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "21.7" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-
-[Term]
-id: XLMOD:02199
-name: BS(PEG)9
-def: "Bis(sulfosuccinimidyl)suberate nonaethyleneglycol." [CAS:1008402-79-6, PubChem_Compound:77078480, ChemSpiderID:29354490, ChemicalBookNo:CB32546994]
-synonym: "NHS-PEG9-NHS" EXACT []
-property_value: hydrophilicPEGchain: "9" xsd:nonNegativeInteger
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "35.8" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-
-[Term]
-id: XLMOD:02200
-name: NHS-azide
-def: "N-hydroxysuccinimide ester ethane azide." [PSI:XL]
-synonym: "Azido-NHS ester" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "2.5" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00055 ! azide
-
-[Term]
-id: XLMOD:02201
-name: NHS-PEG4-azide
-def: "N-hydroxysuccinimide ester tetraoxapentadecane azide." [CAS:944251-24-5, PubChem_Compound:51340931, ChemSpiderID:28604876, ChemicalBookNo:CB72663895]
-synonym: "Azido-PEG4-NHS ester" EXACT []
-property_value: hydrophilicPEGchain: "4" xsd:nonNegativeInteger
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "18.9" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00055 ! azide
-
-[Term]
-id: XLMOD:02202
-name: NHS-PEG12-azide
-def: "N-hydroxysuccinimide ester dodecaoxanonatriacontane azide." [CAS:1610796-02-5, PubChem_Compound:51340930, ChemSpiderID:29354441, ChemicalBookNo:CB63062337]
-synonym: "Azido-PEG12-NHS ester" EXACT []
-property_value: hydrophilicPEGchain: "12" xsd:nonNegativeInteger
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "47.3" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00055 ! azide
-
-[Term]
-id: XLMOD:02203
-name: SPDP-PEG4-NHS ester
-def: "2-pyridyldithiol-tetraoxatetradecane-N-hydroxysuccinimide." [CAS:1334177-95-5, PubChem_Compound:77078429, ChemSpiderID:29354407, ChemicalBookNo:CB83163140]
-synonym: "PEG4-SPDP" EXACT []
-property_value: hydrophilicPEGchain: "4" xsd:nonNegativeInteger
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "25.7" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00109 ! pyridinyldisulfide
-
-[Term]
-id: XLMOD:02204
-name: SPDP-PEG12-NHS ester
-def: "2-pyridyldithiol-tetraoxaoctatriacontane-N-hydroxysuccinimide." [PubChem_Compound:51341026, ChemicalBookNo:CB53163134]
-synonym: "PEG12-SPDP" EXACT []
-property_value: hydrophilicPEGchain: "12" xsd:nonNegativeInteger
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "54.1" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00109 ! pyridinyldisulfide
-
-[Term]
-id: XLMOD:02205
-name: BPM
-def: "4-(N-Maleimido)benzophenone." [CAS:92944-71-3, PubChem_Compound:24897368, MDL:MFCD00079465, ChemSpiderID:129121, ChemicalBookNo:CB6293028]
-synonym: "Benzophenone-4-maleimide" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-relationship: has_reactive_group XLMOD:00119 ! benzophenone
-
-[Term]
-id: XLMOD:02206
-name: TPAL
-def: "1,4-Phthalaldehyde." [CAS:623-27-8, PubChem_Compound:12173, ChemSpiderID:11673, ChemicalBookNo:CB1425781]
-property_value: bridgeFormula: "C8 H6" xsd:string
-property_value: monoIsotopicMass: "102.04695021" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00141 ! carbonyl
-
-[Term]
-id: XLMOD:02207
-name: DEB
-def: "Diformyl-5-ethynylbenzene." [ChemSpiderID:26667536]
-synonym: "4-Ethynylphthalaldehyde" EXACT []
-property_value: bridgeFormula: "C10 H6" xsd:string
-property_value: monoIsotopicMass: "126.04695021" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00141 ! carbonyl
-
-[Term]
-id: XLMOD:02208
-name: DMTMM
-def: "4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride." [CAS:3945-69-5, PubChem_Compound:2734059, ChemSpiderID:2015817, ChemicalBookNo:CB5695021, PMID:24938783]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00146 ! dimethylether
-
-[Term]
-id: XLMOD:02209
-name: PDH
-def: "Pimelic acid dihydrazide." [CAS:13043-98-6, PubChem_Compound:284646, ChemSpiderID:250842, ChemicalBookNo:CB9261011]
-synonym: "Heptanedihydrazide" EXACT []
-property_value: bridgeFormula: "C7 H12 N4" xsd:string
-property_value: monoIsotopicMass: "152.10619642" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00110 ! hydrazide
-
-[Term]
-id: XLMOD:02210
-name: PDH-d10
-def: "Deuterium labelled pimelic acid dihydrazide." [PSI:XL]
-property_value: bridgeFormula: "C7 D10 H2 N4" xsd:string
-property_value: doubletDeltaMass: "10.06276744" xsd:double
-property_value: monoIsotopicMass: "162.16896386" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00110 ! hydrazide
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-
-[Term]
-id: XLMOD:02211
-name: ABAS
-def: "Azidobenzoic acid succinimide." [CAS:53053-08-0, PubChem_Compound:122153, ChemSpiderID:108951, ChemicalBookNo:CB5187007, PMID:25192908]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "7.0" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00055 ! azide
-
-[Term]
-id: XLMOD:02212
-name: ABAS-13C6
-def: "13C labelled azidobenzoic acid succinimide." [PMID:25192908]
-property_value: doubletDeltaMass: "6.02016" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "7.0" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00055 ! azide
-relationship: is_labelled XLMOD:00036 ! 13C labelled
-
-[Term]
-id: XLMOD:02213
-name: CBS
-def: "Carboxy-benzophenone-succinimide." [PMID:25192908]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "7.0" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00119 ! benzophenone
-
-[Term]
-id: XLMOD:02214
-name: CBS-13C6
-def: "13C labelled carboxy-benzophenone-succinimide." [PMID:25192908]
-property_value: doubletDeltaMass: "6.02016" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "7.0" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00119 ! benzophenone
-relationship: is_labelled XLMOD:00036 ! 13C labelled
-
-[Term]
-id: XLMOD:02215
-name: SDA-13C5
-def: "13C labelled succinimidyl-ester diazirine." [PMID:25192908]
-property_value: bridgeFormula: "13C5 H6 O1" xsd:string
-property_value: doubletDeltaMass: "5.0168" xsd:double
-property_value: monoIsotopicMass: "87.05866484" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "5.0" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00103 ! diazirine
-relationship: is_labelled XLMOD:00036 ! 13C labelled
-
-[Term]
-id: XLMOD:02216
-name: DMDSSO
-def: "Dimethyl disuccinimidyl sulfoxide." [PMID:24471733, PMID:27417384]
-synonym: "DMDSSO-d0" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00067 ! CID cleavable C-S bond
-
-[Term]
-id: XLMOD:02217
-name: DMDSSO-d10
-def: "Deuterium labelled dimethyl disuccinimidyl sulfoxide." [PMID:24471733]
-property_value: doubletDeltaMass: "10.06276744" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_cleavable XLMOD:00067 ! CID cleavable C-S bond
-
-[Term]
-id: XLMOD:02218
-name: ICATXL1
-def: "N-biotinyl-N'-[3,5-Bis-(N-succinimidyloxycarbonyl-methoxy)-benzoyl]-ethane-1,2-diamine." [PMID:16895390]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-
-[Term]
-id: XLMOD:02219
-name: ICATXL2
-def: "S-S-biotinyl-N'-[3,5-Bis-(N-succinimidyloxycarbonyl-methoxy)-benzoyl]-ethane-1,2-diamine." [PMID:16895390]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00023 ! cleavable S-S bond
-
-[Term]
-id: XLMOD:02220
-name: SSTN
-def: "Succinic acid succinimidyl ester 5-thioyloxy-2-nitrobenzyl ester." [PMID:15366956]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00148 ! nitrobenzylester
-
-[Term]
-id: XLMOD:02221
-name: SCNE
-def: "Di 6-(3-succinimidyl carbonyloxymethyl-4-nitro-phenoxy)-hexanoic acid disulfide diethanol ester." [PMID:22432929]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00023 ! cleavable S-S bond
-relationship: is_cleavable XLMOD:00147 ! photocleavable
-
-[Term]
-id: XLMOD:02222
-name: azide-A-DSBSO
-def: "Azide-tagged acid-cleavable disuccinimidyl-bissulfoxide." [PMID:25823605, PMID:27417384, PMID:25253489]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_handle XLMOD:00055 ! azide
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00018 ! cleavable by MS2 labile bond
-relationship: is_cleavable XLMOD:00066 ! acid cleavable
-relationship: is_cleavable XLMOD:00067 ! CID cleavable C-S bond
-
-[Term]
-id: XLMOD:02223
-name: alkyne-A-DSBSO
-def: "Alkyne-tagged acid-cleavable disuccinimidyl-bissulfoxide." [PMID:25823605, PMID:29537042]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_handle XLMOD:00053 ! alkyne
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00066 ! acid cleavable
-relationship: is_cleavable XLMOD:00067 ! CID cleavable C-S bond
-
-[Term]
-id: XLMOD:02224
-name: IML 3
-def: "Identical mass linker 3." [PMID:26269432]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00035 ! CID cleavable
-
-[Term]
-id: XLMOD:02225
-name: SuVP
-def: "Disuccinimidyl-succinamyl-valyl-proline." [PMID:26091612, PMID:20560670]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "11.2" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00035 ! CID cleavable
-
-[Term]
-id: XLMOD:02226
-name: DHSO
-def: "Dihydrazide sulfoxide." [PMID:27417384]
-synonym: "3,3'-sulfinyldi(propanehydrazide)" EXACT []
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "12.4" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00110 ! hydrazide
-relationship: is_cleavable XLMOD:00067 ! CID cleavable C-S bond
-
-[Term]
-id: XLMOD:02227
-name: PL
-def: "Photo-cleavable Leiker." [PMID:26952210, PMID:27734140]
-property_value: CID_Fragment: "122.06" xsd:double
-property_value: monoIsotopicMass: "316.14" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00147 ! photocleavable
-
-[Term]
-id: XLMOD:02228
-name: PEG-PL
-def: "Polyethylene glycol photo-cleavable Leiker." [PMID:26952210]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00147 ! photocleavable
-
-[Term]
-id: XLMOD:02229
-name: Sulfo-PL
-def: "Sulfo-photo-cleavable Leiker." [PMID:26952210]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: is_cleavable XLMOD:00147 ! photocleavable
-
-[Term]
-id: XLMOD:02230
-name: bAL1
-def: "Biotinylated azo-Leiker 1 with an azobenzene-based chemical cleavage site." [PMID:26952210]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "9.3" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: is_cleavable XLMOD:00017 ! chemically cleavable
-
-[Term]
-id: XLMOD:02231
-name: bAL2
-def: "Biotinylated azo-Leiker 2 with an azobenzene-based chemical cleavage site." [PMID:26952210]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "9.3" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: is_cleavable XLMOD:00017 ! chemically cleavable
-
-[Term]
-id: XLMOD:02232
-name: bAL2-d6
-def: "Deuterium labelled biotinylated azo-Leiker 2 with an azobenzene-based chemical cleavage site." [PMID:26952210]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "9.3" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: is_cleavable XLMOD:00017 ! chemically cleavable
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-
-[Term]
-id: XLMOD:02233
-name: BS3-18O2
-def: "18O labelled (bis(sulfosuccinimidyl) 2,2,7,7-suberate)." [PMID:14592499]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "11.4" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: is_labelled XLMOD:00069 !  18O labelled
-
-[Term]
-id: XLMOD:02234
-name: PIR-I
-def: "Protein Interaction Reporter-I." [PMID:17269728]
-property_value: bridgeFormula: "C6 H10 O2 N1" xsd:string
-property_value: hydrophilicPEGchain: "3" xsd:nonNegativeInteger
-property_value: monoIsotopicMass: "128.0712" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: reporterMass: "555.2481" xsd:double
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00035 ! CID cleavable
-
-[Term]
-id: XLMOD:02235
-name: PIR-II
-def: "Protein Interaction Reporter-II." [PMID:17269728]
-property_value: bridgeFormula: "C4 H6 O2 N1" xsd:string
-property_value: hydrophilicPEGchain: "3" xsd:nonNegativeInteger
-property_value: monoIsotopicMass: "100.0399" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: reporterMass: "1324.5937" xsd:double
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00035 ! CID cleavable
-
-[Term]
-id: XLMOD:02236
-name: PIR-III
-def: "Protein Interaction Reporter-III." [PMID:17269728]
-property_value: bridgeFormula: "C4 H6 O2 N1" xsd:string
-property_value: hydrophilicPEGchain: "3" xsd:nonNegativeInteger
-property_value: monoIsotopicMass: "100.0399" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: reporterMass: "1604.6996" xsd:double
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00034 ! photo cleavable
-relationship: is_cleavable XLMOD:00035 ! CID cleavable
-
-[Term]
-id: XLMOD:02237
-name: PIR
-def: "Protein Interaction Reporter." [PMID:15623310]
-property_value: CID_Fragment: "711.4" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00035 ! CID cleavable
-
-[Term]
-id: XLMOD:02238
-name: pcPIR
-def: "Photo-cleavable Protein Interaction Reporter." [PMID:20373789]
-property_value: CID_Fragment: "711.4" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "40.0" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00034 ! photo cleavable
-relationship: is_cleavable XLMOD:00035 ! CID cleavable
-
-[Term]
-id: XLMOD:02239
-name: PEG5-Biotin-Dimer
-def: "PEG5-Biotin-Dimer for crosslinking avidin molecules." [PSI:XL]
-property_value: hydrophilicPEGchain: "5" xsd:nonNegativeInteger
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "43.4" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00118 ! tetrafluorophenyl azide
-
-[Term]
-id: XLMOD:02240
-name: Azido-PEG3-NHS ester
-def: "1-[(3-{2-[2-(2-Azidoethoxy)ethoxy]ethoxy}propanoyl)oxy]-2,5-pyrrolidinedione." [CAS:1245718-89-1, PubChem_Compound:77078451, ChemSpiderID:29354443, ChemicalBookNo:CB83062351]
-synonym: "NHS-PEG3-azide" EXACT []
-property_value: hydrophilicPEGchain: "3" xsd:nonNegativeInteger
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00055 ! azide
-
-[Term]
-id: XLMOD:02241
-name: Azido-PEG5-NHS ester
-def: "1-[(1-Azido-18-oxo-3,6,9,12,15-pentaoxaoctadecan-18-yl)oxy]-2,5-pyrrolidinedione." [CAS:1433996-86-1, PubChem_Compound:77078433, ChemSpiderID:29354411, ChemicalBookNo:CB23062364]
-synonym: "NHS-PEG5-azide" EXACT []
-property_value: hydrophilicPEGchain: "5" xsd:nonNegativeInteger
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00055 ! azide
-
-[Term]
-id: XLMOD:02242
-name: Azido-PEG6-NHS ester
-def: "1-[(1-Azido-21-oxo-3,6,9,12,15,18-hexaoxahenicosan-21-yl)oxy]-2,5-pyrrolidinedione." [CAS:2055014-64-5, PubChem_Compound:77078479, ChemSpiderID:29354488, ChemicalBookNo:CB43162882]
-synonym: "NHS-PEG6-azide" EXACT []
-property_value: hydrophilicPEGchain: "6" xsd:nonNegativeInteger
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00055 ! azide
-
-[Term]
-id: XLMOD:02243
-name: Azido-PEG8-NHS ester
-def: "1-[(1-Azido-27-oxo-3,6,9,12,15,18,21,24-octaoxaheptacosan-27-yl)oxy]-2,5-pyrrolidinedione." [CAS:1204834-00-3, PubChem_Compound:51340932, ChemSpiderID:29354442, ChemicalBookNo:CB53062370]
-synonym: "NHS-PEG8-azide" EXACT []
-property_value: hydrophilicPEGchain: "8" xsd:nonNegativeInteger
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00055 ! azide
-
-[Term]
-id: XLMOD:02244
-name: Azido-PEG10-NHS ester
-def: "Azido-PEG10-NHS ester." [PubChem_Compound:134159750]
-synonym: "NHS-PEG10-azide" EXACT []
-property_value: hydrophilicPEGchain: "10" xsd:nonNegativeInteger
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00055 ! azide
-
-[Term]
-id: XLMOD:02245
-name: Azido-PEG16-NHS ester
-def: "Azido-PEG16-NHS ester." [PubChem_Compound:126480441]
-synonym: "NHS-PEG16-azide" EXACT []
-property_value: hydrophilicPEGchain: "16" xsd:nonNegativeInteger
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00055 ! azide
-
-[Term]
-id: XLMOD:02246
-name: Azido-PEG24-NHS ester
-def: "Azido-PEG24-NHS ester." [PubChem_Compound:126480440]
-synonym: "NHS-PEG24-azide" EXACT []
-property_value: hydrophilicPEGchain: "24" xsd:nonNegativeInteger
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00055 ! azide
-
-[Term]
-id: XLMOD:02247
-name: SPDP-PEG24-NHS ester
-def: "2,5-Dioxocyclopentyl 77-oxo-79-(2-pyridinyldisulfanyl)-4,7,10,13,16,19,22,25,28,31,34,37,40,43,46,49,52,55,58,61,64,67,70,73-tetracosaoxa-76-azanonaheptacontan-1-oate." [PubChem_Compound:77078309, ChemSpiderID:32055782, ChemicalBookNo:CB13163136]
-synonym: "PEG24-SPDP" EXACT []
-property_value: hydrophilicPEGchain: "24" xsd:nonNegativeInteger
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00109 ! pyridinyldisulfide
-
-[Term]
-id: XLMOD:02248
-name: S-Methyl 5,5'-thiodipentanoylhydroxysuccinimide
-def: "S-Methyl 5,5'-thiodipentanoylhydroxysuccinimide cross-linker." [PMID:19551991]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00035 ! CID cleavable
-
-[Term]
-id: XLMOD:02249
-name: Sulfo-SBP
-def: "4-(N-Sulfosuccinimidylcarboxy)benzophenone." [CAS:91990-88-4, PMID:28430416]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: specificities: "(K,S,T,Y,Protein N-term)" xsd:string
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: has_reactive_group XLMOD:00119 ! benzophenone
-relationship: is_activatable XLMOD:00149 ! photoactivatable
-
-[Term]
-id: XLMOD:02250
-name: CBSS
-def: "Carboxybenzophenonesulfosuccinimide." [PMID:31045356]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: has_reactive_group XLMOD:00119 ! benzophenone
-
-[Term]
-id: XLMOD:02251
-name: MC4
-def: "1,4-bis(4-((2,5-dioxopyrrolidin-1-yl)oxy)-4-oxobutyl)-1,4-diazabicyclo[2.2.2]octane-1,4-diium." [PMID:31045356, PMID:29537042]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "13.0" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00035 ! CID cleavable
-
-[Term]
-id: XLMOD:02252
-name: PAC4
-def: "PAC4 cross-linker." [PMID:29537042]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "13.0" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00035 ! CID cleavable
-
-[Term]
-id: XLMOD:02253
-name: cliXLink
-def: "cliXLink cross-linker." [PMID:31593346]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "9.2" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_handle XLMOD:00053 ! alkyne
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00035 ! CID cleavable
-
-[Term]
-id: XLMOD:02254
-name: ARGO1
-def: "R-R aromatic glyoxal cross-linker 1." [PMID:31477730]
-property_value: hydrophilicPEGchain: "1" xsd:nonNegativeInteger
-property_value: monoIsotopicMass: "326.079" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "29.4" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00142 ! phenylglyoxal
-
-[Term]
-id: XLMOD:02255
-name: ARGO2
-def: "R-R aromatic glyoxal cross-linker 2." [PMID:31477730]
-property_value: hydrophilicPEGchain: "2" xsd:nonNegativeInteger
-property_value: monoIsotopicMass: "370.105" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "33.7" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00142 ! phenylglyoxal
-
-[Term]
-id: XLMOD:02256
-name: ARGO3
-def: "R-R aromatic glyoxal cross-linker 3." [PMID:31477730]
-property_value: hydrophilicPEGchain: "3" xsd:nonNegativeInteger
-property_value: monoIsotopicMass: "414.131" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "37.7" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00142 ! phenylglyoxal
-
-[Term]
-id: XLMOD:02257
-name: KARGO
-def: "K-R aromatic glyoxal cross-linker." [PMID:31477730]
-property_value: monoIsotopicMass: "352.095" xsd:double
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "54.1" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00142 ! phenylglyoxal
-relationship: has_reactive_group XLMOD:00171 ! Ortho-phthalaldehyde
-
-[Term]
-id: XLMOD:02258
-name: PhoX
-def: "PhoX cross-linker." [PMID:31477730]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: spacerLength: "5.0-20.0" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_handle XLMOD:00173 ! phosphonic acid
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-
-[Term]
-id: XLMOD:03001
-name: CBDPS
-def: "Cyanurbiotindipropionylsuccinimide." [PMID:20622150]
-property_value: bridgeFormula: "C19 H23 N7 O4 S3" xsd:string
-property_value: monoIsotopicMass: "509.09682" xsd:double
-property_value: reactionSites: "3" xsd:nonNegativeInteger
-property_value: spacerLength: "14.0" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_property XLMOD:00014 ! hydrophilic
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_cleavable XLMOD:00035 ! CID cleavable
-
-[Term]
-id: XLMOD:03002
-name: Sulfo-SBED
-def: "Sulfo-SBED cross-linker." [PubChem_Compound:101089650, ChemicalBookNo:CB2771737, PMID:15144972, PMID:16246579, PMID:15144972]
-synonym: "Sulfo-N-hydroxysuccinimidyl-2-(6-[biotinamido]-2-(p-azido benzamido)-hexanoamido) ethyl-1,3'-dithioproprionate" EXACT []
-property_value: monoIsotopicMass: "634.207" xsd:double
-property_value: reactionSites: "3" xsd:nonNegativeInteger
-property_value: spacerLength: "9.1" xsd:float
-property_value: spacerLength: "13.7" xsd:float
-property_value: spacerLength: "19.1" xsd:float
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_reactive_group XLMOD:00102 ! Sulfo NHS ester
-relationship: has_reactive_group XLMOD:00126 ! phenyl azide
-relationship: is_cleavable XLMOD:00023 ! cleavable S-S bond
-
-[Term]
-id: XLMOD:03003
-name: Mts-Atf-Biotin
-def: "2-[N2-(4-Azido-2,3,5,6-tetrafluorobenzoyl)-N6-(6-biotinamidocaproyl)-L-lysinyl]ethylmethanethiosulfate." [CAS:1356383-18-0, PubChem_Compound:57370043, ChemSpiderID:48058836, ChemicalBookNo:CB4994943]
-synonym: "tetrafluorobenzoyl-biotinamidocaproyl-methanethiosulfonate" EXACT []
-property_value: reactionSites: "3" xsd:nonNegativeInteger
-property_value: spacerLength: "11.1" xsd:float
-property_value: spacerLength: "29.3" xsd:float
-property_value: spacerLength: "30.7" xsd:float
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_reactive_group XLMOD:00118 ! tetrafluorophenyl azide
-relationship: has_reactive_group XLMOD:00121 ! methanethiosulfonate 
-relationship: is_cleavable XLMOD:00023 ! cleavable S-S bond
-
-[Term]
-id: XLMOD:03004
-name: Mts-Atf-LC-Biotin
-def: "2-{N2-[N6-(4-Azido-2,3,5,6-tetrafluorobenzoyl)-N6-(6-biotinamidocaproyl)-L-lysinyl]}ethylmethanethiosulfate." [PSI:XL]
-synonym: "Mts-Atf-Long Chain-Biotin" EXACT []
-property_value: reactionSites: "3" xsd:nonNegativeInteger
-property_value: spacerLength: "11.1" xsd:float
-property_value: spacerLength: "29.3" xsd:float
-property_value: spacerLength: "30.7" xsd:float
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_reactive_group XLMOD:00118 ! tetrafluorophenyl azide
-relationship: has_reactive_group XLMOD:00121 ! methanethiosulfonate 
-
-[Term]
-id: XLMOD:03005
-name: TSAT
-def: "Tris-succinimidyl aminotriacetate." [CAS:401514-72-5, PubChem_Compound:4150925, MDL:MFCD02258953, ChemSpiderID:3363127, ChemicalBookNo:CB8454500]
-property_value: reactionSites: "3" xsd:nonNegativeInteger
-property_value: spacerLength: "4.2" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-
-[Term]
-id: XLMOD:03006
-name: SBED
-def: "SBED cross-linker." [PSI:XL]
-synonym: "N-hydroxysuccinimidyl-2-(6-[biotinamido]-2-(p-azido benzamido)-hexanoamido) ethyl-1,3'-dithioproprionate" EXACT []
-property_value: reactionSites: "3" xsd:nonNegativeInteger
-property_value: spacerLength: "9.1" xsd:float
-property_value: spacerLength: "13.7" xsd:float
-property_value: spacerLength: "19.1" xsd:float
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00126 ! phenyl azide
-relationship: is_cleavable XLMOD:00023 ! cleavable S-S bond
-
-[Term]
-id: XLMOD:03007
-name: TMEA
-def: "Tris-(2-maleimidoethyl)amine." [CAS:139112-38-2, PubChem_Compound:9977418, MDL:MFCD01868689, ChemSpiderID:8153010, ChemicalBookNo:CB8193391]
-property_value: reactionSites: "3" xsd:nonNegativeInteger
-property_value: spacerLength: "10.3" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:03008
-name: TRICEPS
-def: "TRICEPS cross-linker." [PubChem_Compound:72663594, PMID:23051814]
-property_value: reactionSites: "3" xsd:nonNegativeInteger
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00143 ! hydrazone
-relationship: is_cleavable XLMOD:00024 ! periodate cleavable
-
-[Term]
-id: XLMOD:03009
-name: NNP9
-def: "NNP9 cross-linker." [PMID:25522193]
-property_value: bridgeFormula: "C7 D10 H2 N4" xsd:string
-property_value: monoIsotopicMass: "314.1127" xsd:double
-property_value: reactionSites: "3" xsd:nonNegativeInteger
-property_value: spacerLength: "10.0" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: has_reactive_group XLMOD:00055 ! azide
-
-[Term]
-id: XLMOD:03010
-name: TATA
-def: "2,4,6-triazido-1,3,5-triazine." [CAS:5637-83-2, PubChem_Compound:21857, ChemSpiderID:20543, ChemicalBookNo:CB82442831, PMID:26931439]
-synonym: "Cyanuric triazide" EXACT []
-property_value: monoIsotopicMass: "200.05" xsd:double
-property_value: reactionSites: "3" xsd:nonNegativeInteger
-property_value: spacerLength: "5.0" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00055 ! azide
-
-[Term]
-id: XLMOD:03011
-name: TATA-13C6
-def: "13C labelled 2,4,6-triazido-1,3,5-triazine." [PMID:26931439]
-property_value: doubletDeltaMass: "6.02016" xsd:double
-property_value: monoIsotopicMass: "206.07016" xsd:double
-property_value: reactionSites: "3" xsd:nonNegativeInteger
-property_value: spacerLength: "5.0" xsd:float
-is_a: XLMOD:00005 ! homofunctional cross-linker
-relationship: has_reactive_group XLMOD:00055 ! azide
-relationship: is_labelled XLMOD:00036 ! 13C labelled
-
-[Term]
-id: XLMOD:03012
-name: MRN
-def: "MRN cross-linker." [PMID:18303833]
-property_value: reactionSites: "3" xsd:nonNegativeInteger
-property_value: spacerLength: "6.4" xsd:float
-property_value: spacerLength: "11.4" xsd:float
-property_value: spacerLength: "40.0" xsd:float
-is_a: XLMOD:00006 ! heterofunctional cross-linker
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-
-[Term]
-id: XLMOD:03013
-name: Mts-Atf-Biotin-LC
-def: "Long chain Mts-Atf-Biotin." [PSI:XL]
-property_value: reactionSites: "3" xsd:nonNegativeInteger
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_reactive_group XLMOD:00118 ! tetrafluorophenyl azide
-relationship: has_reactive_group XLMOD:00121 ! methanethiosulfonate 
-relationship: is_cleavable XLMOD:00023 ! cleavable S-S bond
-
-[Term]
-id: XLMOD:03014
-name: DADPS linker
-def: "Linker containing a dialkoxydiphenylsilane group." [PMID:31430117]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: specificities: "(C,U)" xsd:string
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_reactive_group XLMOD:00055 ! azide
-is_a: XLMOD:00099 ! formic acid cleavable
-
-[Term]
-id: XLMOD:03015
-name: AZO linker
-def: "Linker containing a azobenzene group." [PMID:31430117]
-property_value: reactionSites: "2" xsd:nonNegativeInteger
-property_value: specificities: "(C,U)" xsd:string
-is_a: XLMOD:00003 ! label transfer reagent
-relationship: has_handle XLMOD:00051 ! biotin
-relationship: has_reactive_group XLMOD:00055 ! azide
-is_a: XLMOD:00169 ! sodium dithionite cleavable
-
-[Term]
-id: XLMOD:06000
-name: derivatization entity
-def: "Entity relevant to the domain of derivatization in chromatography." [PSI:XL]
-relationship: part_of XLMOD:00000 ! Proteomics Standards Initiative cross-linking and derivatization controlled vocabulary
-
-[Term]
-id: XLMOD:06001
-name: GCMS derivatization reagent
-def: "Chemical reagent, which transforms a polar group in a molecule into a non-polar group in order to make the molecule volatile and analyzable by GC-MS." [PSI:XL]
-is_a: XLMOD:06000 ! derivatization entity
-
-[Term]
-id: XLMOD:06002
-name: alkylation reagent
-def: "Derivatization reagent replacing an active hydrogen by an aliphatic or aliphatic-aromatic group." [PSI:XL]
-is_a: XLMOD:06001 ! GCMS derivatization reagent
-
-[Term]
-id: XLMOD:06003
-name: silylation reagent
-def: "Silylation reagent replacing an active hydrogen by a silyl group." [PSI:XL]
-is_a: XLMOD:06001 ! GCMS derivatization reagent
-
-[Term]
-id: XLMOD:06004
-name: acylation reagent
-def: "Acylation reagent replacing an active hydrogen by a acyl (R-C=O-) group." [PSI:XL]
-is_a: XLMOD:06001 ! GCMS derivatization reagent
-
-[Term]
-id: XLMOD:06005
-name: fluorinated anhydride reagent
-def: "Fluorinated anhydride derivatization reagent." [PSI:XL]
-is_a: XLMOD:06004 ! acylation reagent
-
-[Term]
-id: XLMOD:06006
-name: fluoracylimidazole reagent
-def: "Fluoracylimidazole derivatization reagent." [PSI:XL]
-is_a: XLMOD:06004 ! acylation reagent
-
-[Term]
-id: XLMOD:06008
-name: halomethylsilyl reagent
-def: "Halogenation reagent which can produce both silylated and halogenated derivatives." [PSI:XL]
-is_a: XLMOD:06003 ! silylation reagent
-
-[Term]
-id: XLMOD:06009
-name: chiral derivatization reagent
-def: "Chiral derivatization reagent with an enatiomerically pure chiral derivatizing agent to form two diastereomeric derivatives that can be separated by gas chromatography." [PSI:XL]
-is_a: XLMOD:06001 ! GCMS derivatization reagent
-
-[Term]
-id: XLMOD:06010
-name: LCMS derivatization reagent
-def: "Chemical reagent, which transforms an analyte so that its stability, separation, extraction, ionization efficiency and MS2 detectability are improved in LC-MS analysis." [PSI:XL]
-is_a: XLMOD:06000 ! derivatization entity
-
-[Term]
-id: XLMOD:06011
-name: dialkylacetal
-def: "Dialkylacetal reagent." [PSI:XL]
-is_a: XLMOD:06002 ! alkylation reagent
-
-[Term]
-id: XLMOD:06012
-name: diazoalkal
-def: "Diazoalkal reagent." [PSI:XL]
-is_a: XLMOD:06002 ! alkylation reagent
-
-[Term]
-id: XLMOD:06013
-name: TMS reagent
-def: "Trimethylsilyl (TMS) reagent replacing an active hydrogen by a silyl group." [PSI:XL]
-is_a: XLMOD:06003 ! silylation reagent
-
-[Term]
-id: XLMOD:06014
-name: DMS reagent
-def: "Dimethylsilyl (DMS) reagent replacing an active hydrogen by a silyl group." [PSI:XL]
-is_a: XLMOD:06003 ! silylation reagent
-
-[Term]
-id: XLMOD:06015
-name: TFA reagent
-def: "Trifluoroacetyl (TFA) reagent replacing an active hydrogen by a silyl group." [PSI:XL]
-is_a: XLMOD:06004 ! acylation reagent
-
-[Term]
-id: XLMOD:06016
-name: boron trifluoride reagent
-def: "Boron trifluoride reagent." [PSI:XL]
-is_a: XLMOD:06002 ! alkylation reagent
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:06017
-name: N,N-Dimethylformamidedialkyl acetal
-def: "N,N-Dimethylformamidedialkyl acetal." [PSI:XL]
-is_a: XLMOD:06002 ! alkylation reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:06018
-name: chloroformate reagent
-def: "Chloroformate reagent." [PSI:XL]
-is_a: XLMOD:06002 ! alkylation reagent
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00163 ! chloroformate reactive group
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-relationship: is_reactive_with XLMOD:06509 ! phenol reactive
-relationship: is_reactive_with XLMOD:06513 ! thiol reactive
-
-[Term]
-id: XLMOD:06019
-name: trialkyloxonium reagent
-def: "Trialkyloxonium reagent." [PSI:XL]
-is_a: XLMOD:06002 ! alkylation reagent
-
-[Term]
-id: XLMOD:06020
-name: arylation reagent
-def: "Derivatization reagent replacing an active hydrogen by an aliphatic-aromatic group, e.g. a -phenyl, -tolyl, -xylyl, -naphthy, -benzyl group." [PSI:XL]
-is_a: XLMOD:06002 ! alkylation reagent
-
-[Term]
-id: XLMOD:06100
-name: chromophore
-def: "A chromophore group attached to a derivatization reagent for enhanced UB- or VIS-detectability." [DOI:10.1016/B978-0-12-415806-1.00002-4]
-is_a: XLMOD:06000 ! derivatization entity
-
-[Term]
-id: XLMOD:06101
-name: fluorophore
-def: "A fluorophore group attached to a derivatization reagent for enhanced fluorescence or chemiluminescence detectability." [DOI:10.1016/B978-0-12-415806-1.00002-4]
-is_a: XLMOD:06000 ! derivatization entity
-
-[Term]
-id: XLMOD:06102
-name: electrophore
-def: "An electrophore group attached to a derivatization reagent for enhanced electrochemical detectability." [DOI:10.1016/B978-0-12-415806-1.00002-4]
-is_a: XLMOD:06000 ! derivatization entity
-
-[Term]
-id: XLMOD:06103
-name: 4-nitrophenyl
-def: "4-Nitrophenyl fluorophore." [DOI:10.1016/B978-0-12-415806-1.00002-4]
-is_a: XLMOD:06101 ! fluorophore
-property_value: maxAbsorption: "265 nm" xsd:string
-
-[Term]
-id: XLMOD:06104
-name: 2,4-dinitrophenyl
-def: "2,4-Dinitrophenyl fluorophore." [PSI:XL]
-is_a: XLMOD:06101 ! fluorophore
-
-[Term]
-id: XLMOD:06105
-name: 3,5-dinitrobenzyl
-def: "3,5-Dinitrobenzyl fluorophore." [DOI:10.1016/B978-0-12-415806-1.00002-4]
-is_a: XLMOD:06101 ! fluorophore
-
-[Term]
-id: XLMOD:06106
-name: 4-chlorobenzoate
-def: "4-Chlorobenzoatel fluorophore." [DOI:10.1016/B978-0-12-415806-1.00002-4]
-is_a: XLMOD:06101 ! fluorophore
-property_value: maxAbsorption: "236 nm" xsd:string
-
-[Term]
-id: XLMOD:06107
-name: 4-nitrobenzoate
-def: "4-Nitrobenzoatel fluorophore." [DOI:10.1016/B978-0-12-415806-1.00002-4]
-is_a: XLMOD:06101 ! fluorophore
-property_value: maxAbsorption: "254 nm" xsd:string
-
-[Term]
-id: XLMOD:06108
-name: toluoyl
-def: "Toluoyll fluorophore." [DOI:10.1016/B978-0-12-415806-1.00002-4]
-is_a: XLMOD:06101 ! fluorophore
-property_value: maxAbsorption: "236 nm" xsd:string
-
-[Term]
-id: XLMOD:06109
-name: anisyl
-def: "Anisyl fluorophore." [DOI:10.1016/B978-0-12-415806-1.00002-4]
-is_a: XLMOD:06101 ! fluorophore
-property_value: maxAbsorption: "262 nm" xsd:string
-
-[Term]
-id: XLMOD:06110
-name: phenacyl
-def: "Phenacyl fluorophore." [DOI:10.1016/B978-0-12-415806-1.00002-4]
-is_a: XLMOD:06101 ! fluorophore
-property_value: maxAbsorption: "250 nm" xsd:string
-
-[Term]
-id: XLMOD:06111
-name: 4-bromophenacyl
-def: "4-Bromophenacyl fluorophore." [DOI:10.1016/B978-0-12-415806-1.00002-4]
-is_a: XLMOD:06101 ! fluorophore
-property_value: maxAbsorption: "260 nm" xsd:string
-
-[Term]
-id: XLMOD:06112
-name: 2-naphthacyl
-def: "2-Naphthacyl fluorophore." [DOI:10.1016/B978-0-12-415806-1.00002-4]
-is_a: XLMOD:06101 ! fluorophore
-property_value: maxAbsorption: "248 nm" xsd:string
-
-[Term]
-id: XLMOD:06500
-name: secondary amine reactive
-def: "Indicates that a reactive group is reactive with secondary amino (=NH) groups." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:06501
-name: active hydrogen reactive
-def: "Indicates that a derivatization reagent is reactive with active hydrogens like e.g. from -SH, -OH, -NH, -COOH groups." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:06502
-name: amide reactive
-def: "Indicates that a derivatization reagent is reactive with amides." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:06503
-name: amino acid reactive
-def: "Indicates that a derivatization reagent is reactive with amino acids." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:06504
-name: nitrosamine reactive
-def: "Indicates that a derivatization reagent is reactive with nitrosamines." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:06505
-name: sulfonamide reactive
-def: "Indicates that a derivatization reagent is reactive with sulfonamides." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:06506
-name: carbohydrate reactive
-def: "Indicates that a derivatization reagent is reactive with carbohydrates and sugars." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:06507
-name: catecholamine reactive
-def: "Indicates that a derivatization reagent is reactive with catecholamines." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:06508
-name: sulfide reactive
-def: "Indicates that a derivatization reagent is reactive with sulfides." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:06509
-name: phenol reactive
-def: "Indicates that a derivatization reagent is reactive with phenols." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:06510
-name: ketone reactive
-def: "Indicates that a derivatization reagent is reactive with ketones." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:06511
-name: biphosphonate drug reactive
-def: "Indicates that a derivatization reagent is reactive with biphosphonate drugs." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:06512
-name: steroid reactive
-def: "Indicates that a derivatization reagent is reactive with steroids." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:06513
-name: thiol reactive
-def: "Indicates that a derivatization reagent is reactive with thiols." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:06514
-name: Vitamin D metabolite reactive
-def: "Indicates that a derivatization reagent is reactive with vitamin D metabolites." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:06515
-name: nucleoside reactive
-def: "Indicates that a derivatization reagent is reactive with nucleosides." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:06516
-name: cholesterol reactive
-def: "Indicates that a derivatization reagent is reactive with cholesterols." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:06517
-name: histamine reactive
-def: "Indicates that a derivatization reagent is reactive with histamines." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:06518
-name: glycan reactive
-def: "Indicates that a derivatization reagent is reactive with glycans." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:06519
-name: alpha-keto acid reactive
-def: "Indicates that a derivatization reagent is reactive with alpha-keto-acids." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:06520
-name: citric acid reactive
-def: "Indicates that a derivatization reagent is reactive with citric acid." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:06521
-name: phophate reactive
-def: "Indicates that a derivatization reagent is reactive with phosphate." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:06522
-name: perfluorinated carboxylic acid reactive
-def: "Indicates that a derivatization reagent is reactive with perfluorinated carboxylic acids." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:06523
-name: sialic acid reactive
-def: "Indicates that a derivatization reagent is reactive with sialic acid." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:06524
-name: bile acid reactive
-def: "Indicates that a derivatization reagent is reactive with bile acids." [PSI:XL]
-is_a: XLMOD:00027 ! chemically reactive
-
-[Term]
-id: XLMOD:07000
-name: dimethylformamide
-def: "Dimethylformamide." [CAS:68-12-2, PubChem_Compound:6228, MDL:MFCD00003284, ChemSpiderID:5993, ChemicalBookNo:CB2854115, DOI:10.5772/33098]
-synonym: "DMF" EXACT []
-is_a: XLMOD:06011 ! dialkylacetal
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06501 ! active hydrogen reactive
-relationship: is_reactive_with XLMOD:06502 ! amide reactive
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-relationship: is_reactive_with XLMOD:06504 ! nitrosamine reactive
-
-[Term]
-id: XLMOD:07001
-name: diazomethane
-def: "Diazomethane." [CAS:334-88-3, PubChem_Compound:9550, ChemSpiderID:9176, ChemicalBookNo:CB4852342, DOI:10.5772/33098]
-is_a: XLMOD:06012 ! diazoalkal
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-relationship: is_reactive_with XLMOD:06511 ! biphosphonate drug reactive
-
-[Term]
-id: XLMOD:07002
-name: pentafluorobenzyl bromide
-def: "Pentafluorobenzyl bromide." [CAS:1765-40-8, PubChem_Compound:74484, MDL:MFCD00000299, ChemSpiderID:67069, ChemicalBookNo:CB9238273, DOI:10.5772/33098, PMID:22191594]
-synonym: "PFBBr" EXACT []
-is_a: XLMOD:06020 ! arylation reagent
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00168 ! benzyl bromide reactive group
-relationship: is_reactive_with XLMOD:06504 ! nitrosamine reactive
-relationship: is_reactive_with XLMOD:06505 ! sulfonamide reactive
-
-[Term]
-id: XLMOD:07003
-name: pentafluorobenzylhydroxylaminehydrochloride
-def: "Pentafluorobenzylhydroxylaminehydrochloride." [CAS:57981-02-9, PubChem_Compound:129670358, Beilstein:4031190, MDL:MFCD00012953, ChemicalBookNo:CB8307815, DOI:10.5772/33098]
-synonym: "PFBHA" EXACT []
-is_a: XLMOD:06020 ! arylation reagent
-relationship: is_reactive_with XLMOD:00063 ! carbonyl reactive
-
-[Term]
-id: XLMOD:07004
-name: benzylbromide
-def: "Benzylbromide." [CAS:100-39-0, PubChem_Compound:7498, ChemSpiderID:13851576, ChemicalBookNo:CB6761035, DOI:10.5772/33098]
-synonym: "BnBr" EXACT []
-is_a: XLMOD:06020 ! arylation reagent
-relationship: has_reactive_group XLMOD:00168 ! benzyl bromide reactive group
-
-[Term]
-id: XLMOD:07005
-name: tetrabutylammoniumhydroxide
-def: "Tetrabutylammoniumhydroxide." [CAS:2052-49-5, PubChem_Compound:2723671, MDL:MFCD00009425, ChemSpiderID:13851576, ChemicalBookNo:CB6371870, DOI:10.5772/33098]
-synonym: "TBH" EXACT []
-is_a: XLMOD:06002 ! alkylation reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-relationship: is_reactive_with XLMOD:06501 ! active hydrogen reactive
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-
-[Term]
-id: XLMOD:07006
-name: boron trifluoride
-def: "Boron trifluoride derivatization reagent." [CAS:7637-07-2, MDL:MFCD00011316, ChemSpiderID:6116, ChemicalBookNo:CB3238105, DOI:10.5772/33098]
-synonym: "BF3" EXACT []
-is_a: XLMOD:06016 ! boron trifluoride reagent
-
-[Term]
-id: XLMOD:07007
-name: bis(trimethylsilyl)acetamide
-def: "Bis(trimethylsilyl)acetamide." [CAS:10416-59-8, PubChem_Compound:6913588, Beilstein:1306669, MDL:MFCD00008270, ChemSpiderID:4523073, ChemicalBookNo:CB7366985, DOI:10.5772/33098]
-synonym: "BSA" EXACT []
-synonym: "N,O-Bis(trimethylsilyl)acetamide" EXACT []
-is_a: XLMOD:06013 ! TMS reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06502 ! amide reactive
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-
-[Term]
-id: XLMOD:07008
-name: bis(trimethylsilyl)trifluoroacetamide
-def: "Bis(trimethylsilyl)trifluoroacetamide." [CAS:25561-30-2, PubChem_Compound:94358, ChemSpiderID:58770, ChemicalBookNo:CB5464744, DOI:10.5772/33098]
-synonym: "BSTFA" EXACT []
-is_a: XLMOD:06013 ! TMS reagent
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:00029 ! sulfhydryl reactive
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06501 ! active hydrogen reactive
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-relationship: is_reactive_with XLMOD:06504 ! nitrosamine reactive
-
-[Term]
-id: XLMOD:07009
-name: N-methyl-trimethylsilyltrifluoroacetamide
-def: "N-methyl-trimethylsilyltrifluoroacetamide." [CAS:24589-78-4, PubChem_Compound:32510, Beilstein:1941550, MDL:MFCD00000411, ChemSpiderID:30134, ChemicalBookNo:CB0161574, DOI:10.5772/33098, PMID:26478271]
-synonym: "MSTFA" EXACT []
-is_a: XLMOD:06013 ! TMS reagent
-relationship: is_reactive_with XLMOD:00029 ! sulfhydryl reactive
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06501 ! active hydrogen reactive
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:07010
-name: hexamethyldisilazane
-def: "Hexamethyldisilazane." [CAS:999-97-3, PubChem_Compound:13838, ChemSpiderID:13238, ChemicalBookNo:CB9105784, DOI:10.5772/33098]
-synonym: "HMDS" EXACT []
-is_a: XLMOD:06003 ! silylation reagent
-relationship: is_reactive_with XLMOD:00029 ! sulfhydryl reactive
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06501 ! active hydrogen reactive
-relationship: is_reactive_with XLMOD:06506 ! carbohydrate reactive
-
-[Term]
-id: XLMOD:07011
-name: trimethylchlorosilane
-def: "Trimethylchlorosilane." [CAS:75-77-4, PubChem_Compound:6397, Beilstein:1209232, MDL:MFCD00000502, ChemSpiderID:6157, ChemicalBookNo:CB4375627, PMID:19525080, DOI:10.5772/33098]
-synonym: "TMCS" EXACT []
-synonym: "CMTS" EXACT []
-synonym: "Chlorotrimethylsilane" EXACT []
-is_a: XLMOD:06013 ! TMS reagent
-relationship: is_reactive_with XLMOD:00029 ! sulfhydryl reactive
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06501 ! active hydrogen reactive
-relationship: is_reactive_with XLMOD:06506 ! carbohydrate reactive
-
-[Term]
-id: XLMOD:07012
-name: trimethylsilylimidazole
-def: "Trimethylsilylimidazole." [CAS:18156-74-6, PubChem_Compound:28925, Beilstein:606148, MDL:MFCD00005280, ChemSpiderID:26905, ChemicalBookNo:CB5483743, DOI:10.5772/33098, PMID:26478271]
-synonym: "TMSI" EXACT []
-synonym: "TMSIM" EXACT []
-synonym: "1-(Trimethylsilyl)imidazole" EXACT []
-is_a: XLMOD:06013 ! TMS reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06501 ! active hydrogen reactive
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-relationship: is_reactive_with XLMOD:06506 ! carbohydrate reactive
-relationship: is_reactive_with XLMOD:06507 ! catecholamine reactive
-relationship: is_reactive_with XLMOD:06508 ! sulfide reactive
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:07013
-name: trimethylsilyldiethylamine
-def: "Trimethylsilyldiethylamine." [CAS:996-50-9, PubChem_Compound:70454, ChemSpiderID:63633, ChemicalBookNo:CB3771284, DOI:10.5772/33098]
-synonym: "TMS-DEA" EXACT []
-is_a: XLMOD:06013 ! TMS reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-relationship: is_reactive_with XLMOD:06501 ! active hydrogen reactive
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-
-[Term]
-id: XLMOD:07014
-name: N-methyl-N-t-butyldimethylsilyltrifluoroacetamide
-def: "N-methyl-N-t-butyldimethylsilyltrifluoroacetamide." [CAS:77377-52-7, PubChem_Compound:2724275, Beilstein:3606546, MDL:MFCD00009671, ChemSpiderID:2006425, ChemicalBookNo:CB7707814, DOI:10.5772/33098, PMID:26478271]
-synonym: "MTBSTFA" EXACT []
-synonym: "1,3-Dimethyl-1,1,3,3-tetraphenyldisilazane" EXACT []
-is_a: XLMOD:06014 ! DMS reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-relationship: is_reactive_with XLMOD:06501 ! active hydrogen reactive
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:07015
-name: trifluoroacetoic anhydride
-def: "Trifluoroacetoic anhydride." [CAS:407-25-0, PubChem_Compound:9845, DOI:10.5772/33098]
-synonym: "TFAA" EXACT []
-is_a: XLMOD:06005 ! fluorinated anhydride reagent
-is_a: XLMOD:06015 ! TFA reagent
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06501 ! active hydrogen reactive
-
-[Term]
-id: XLMOD:07016
-name: pentafluoropropionic anhydride
-def: "Pentafluoropropionic anhydride." [CAS:356-42-3, PubChem_Compound:67742, Beilstein:1806446, MDL:MFCD00000429, ChemicalBookNo:CB2749284, DOI:10.5772/33098]
-synonym: "PFPA" EXACT []
-is_a: XLMOD:06005 ! fluorinated anhydride reagent
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06501 ! active hydrogen reactive
-relationship: is_reactive_with XLMOD:06504 ! nitrosamine reactive
-relationship: is_reactive_with XLMOD:06507 ! catecholamine reactive
-
-[Term]
-id: XLMOD:07017
-name: heptafluorobutyric anhydride
-def: "Heptafluorobutyric anhydride." [CAS:336-59-4, PubChem_Compound:67643, Beilstein:856036, MDL:MFCD00000432, ChemSpiderID:60962, ChemicalBookNo:CB5217287, DOI:10.5772/33098, PMID:26478271]
-synonym: "HFBA" EXACT []
-is_a: XLMOD:06005 ! fluorinated anhydride reagent
-relationship: is_reactive_with XLMOD:06501 ! active hydrogen reactive
-relationship: is_reactive_with XLMOD:06504 ! nitrosamine reactive
-relationship: is_reactive_with XLMOD:06505 ! sulfonamide reactive
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:07018
-name: trifluoroacetylimidazole
-def: "Trifluoroacetylimidazole." [CAS:1546-79-8, PubChem_Compound:73767, Beilstein:608904, MDL:MFCD00014501, ChemSpiderID:66407, ChemicalBookNo:CB7308204, DOI:10.5772/33098]
-synonym: "TFAI" EXACT []
-is_a: XLMOD:06005 ! fluoracylimidazole reagent
-is_a: XLMOD:06015 ! TFA reagent
-relationship: is_reactive_with XLMOD:06501 ! active hydrogen reactive
-
-[Term]
-id: XLMOD:07019
-name: pentafluoropropanylimidazole
-def: "Pentafluoropropanylimidazole." [DOI:10.5772/33098]
-synonym: "PFPI" EXACT []
-is_a: XLMOD:06005 ! fluoracylimidazole reagent
-relationship: is_reactive_with XLMOD:06501 ! active hydrogen reactive
-
-[Term]
-id: XLMOD:07020
-name: heptafluorobutyrylimidazole
-def: "Heptafluorobutyrylimidazole." [CAS:32477-35-3, PubChem_Compound:94431, MDL:MFCD00014503, ChemSpiderID:85218, ChemicalBookNo:CB4100522, DOI:10.5772/33098]
-synonym: "HFBI" EXACT []
-is_a: XLMOD:06005 ! fluoracylimidazole reagent
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06501 ! active hydrogen reactive
-relationship: is_reactive_with XLMOD:06502 ! amide reactive
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-relationship: is_reactive_with XLMOD:06507 ! catecholamine reactive
-
-[Term]
-id: XLMOD:07021
-name: N-Methyl-bis(trifluoroacetamide)
-def: "N-Methyl-bis(trifluoroacetamide)." [CAS:685-27-8, PubChem_Compound:69635, Beilstein:1878402, MDL:MFCD00000412, ChemSpiderID:62836, ChemicalBookNo:CB0220312, DOI:10.5772/33098]
-synonym: "MBTFA" EXACT []
-is_a: XLMOD:06015 ! TFA reagent
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06501 ! active hydrogen reactive
-
-[Term]
-id: XLMOD:07022
-name: pentafluorobenzoyl chloride
-def: "Pentafluorobenzoyl chloride." [CAS:2251-50-5, PubChem_Compound:75256, Beilstein:2054397, MDL:MFCD00000657, ChemSpiderID:67799, ChemicalBookNo:CB6191348, DOI:10.5772/33098]
-synonym: "PFBC" EXACT []
-is_a: XLMOD:06003 ! acylation reagent
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00155 ! acyl chloride
-
-[Term]
-id: XLMOD:07023
-name: pentafluoropropanol
-def: "Pentafluoropropanol." [CAS:679-86-7, PubChem_Compound:168785, MDL:MFCD00153226, ChemSpiderID:9488, ChemicalBookNo:CB9689963, DOI:10.5772/33098]
-synonym: "PFPOH" EXACT []
-is_a: XLMOD:06003 ! acylation reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-relationship: is_reactive_with XLMOD:06501 ! active hydrogen reactive
-
-[Term]
-id: XLMOD:07024
-name: 4-Carbethoxyhexafluorobutyrylchloride
-def: "4-Carbethoxyhexafluorobutyrylchloride." [CAS:18381-53-8, PubChem_Compound:161251, ChemSpiderID:141651, ChemicalBookNo:CB2153034, DOI:10.5772/33098]
-synonym: "4-CB" EXACT []
-is_a: XLMOD:06003 ! acylation reagent
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:07025
-name: N-trifluoroacetyl-L-prolylchloride
-def: "N-trifluoroacetyl-L-prolylchloride." [CAS:36724-68-2, PubChem_Compound:3082449, ChemicalBookNo:CB1411487, DOI:10.5772/33098]
-synonym: "TPC" EXACT []
-is_a: XLMOD:06009 ! chiral derivatization reagent
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:07026
-name: (S)-(-)-N-(Trifluoroacetyl)-prolylchloride
-def: "(S)-(-)-N-(Trifluoroacetyl)-prolylchloride." [CAS:36724-68-2, PubChem_Compound:3082449, ChemicalBookNo:3082449, DOI:10.5772/33098]
-synonym: "I-TPC" EXACT []
-is_a: XLMOD:06009 ! chiral derivatization reagent
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:07027
-name: (-)-alpha-Methoxy-alpha-trifluoromethylphenylacetic acid
-def: "(-)-alpha-Methoxy-alpha-trifluoromethylphenylacetic acid." [CAS:56135-03-6, PubChem_Compound:2723917, MDL:MFCD00066637, DOI:10.5772/33098]
-synonym: "MTPA" EXACT []
-is_a: XLMOD:06009 ! chiral derivatization reagent
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:07028
-name: oximation reagent
-def: "Oximation reagent replacing an aldehyde keto group with an O-methyloxime group." [PSI:XL]
-is_a: XLMOD:06001 ! GCMS derivatization reagent
-
-[Term]
-id: XLMOD:07029
-name: methoxylamine hydrochloride
-def: "Methoxylamine hydrochloride." [CAS:593-56-6, PubChem_Compound:521874, MDL:MFCD00012951, Beilstein:3589723, ChemSpiderID:455236, ChemicalBookNo:CB3439014]
-synonym: "O-Methylhydroxylamine hydrochloride" EXACT []
-synonym: "Methoxyammonium chloride" EXACT []
-is_a: XLMOD:06002 ! alkylation reagent
-is_a: XLMOD:07028 ! oximation reagent
-relationship: is_reactive_with XLMOD:00031 ! aldehyde reactive
-relationship: is_reactive_with XLMOD:06506 ! carbohydrate reactive
-
-[Term]
-id: XLMOD:07030
-name: Trimethyliodosilane
-def: "Trimethyliodosilane." [PMID:26478271, PMID:26478271]
-synonym: "TMIS" EXACT []
-is_a: XLMOD:06009 ! chiral derivatization reagent
-is_a: XLMOD:06013 ! TMS reagent
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:07031
-name: deuterium labelled N-methyl-trimethylsilyltrifluoroacetamide
-def: "Deuterium labelled N-methyl-trimethylsilyltrifluoroacetamide." [CAS:945623-67-6, ChemicalBookNo:CB72545465, PMID:23628173]
-synonym: "MSTFA-d9" EXACT []
-is_a: XLMOD:06013 ! TMS reagent
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_reactive_with XLMOD:00029 ! sulfhydryl reactive
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06501 ! active hydrogen reactive
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:07032
-name: deuterium labelled N-methyl-N-t-butyldimethylsilyltrifluoroacetamide
-def: "Deuterium labelled N-methyl-N-t-butyldimethylsilyltrifluoroacetamide." [PMID:23628173]
-synonym: "MTBSTFA-d6" EXACT []
-is_a: XLMOD:06014 ! DMS reagent
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-relationship: is_reactive_with XLMOD:06501 ! active hydrogen reactive
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:07033
-name: deuterium labelled methyl chloroformate
-def: "Deuterium labelled methyl chloroformate." [PMID:23628173]
-synonym: "MCF-d3" EXACT []
-is_a: XLMOD:06018 ! chloroformate reagent
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-
-[Term]
-id: XLMOD:07034
-name: methyl chloroformate
-def: "Methyl chloroformate." [CAS:79-22-1, PubChem_Compound:6586, ChemSpiderID:6337]
-synonym: "MCF" EXACT []
-is_a: XLMOD:06018 ! chloroformate reagent
-
-[Term]
-id: XLMOD:07035
-name: 9-Fluorenylmethyl chloroformate
-def: "9-Fluorenylmethyl chloroformate." [CAS:28920-43-6, ChemSpiderID:31647, ChemicalBookNo:CB7234569]
-is_a: XLMOD:06018 ! chloroformate reagent
-
-[Term]
-id: XLMOD:07036
-name: trichloroethyl chloroformate
-def: "Trichloroethyl chloroformate." [CAS:17341-93-4, PubChem_Compound:87063, ChemSpiderID:78534, ChemicalBookNo:CB1372973]
-synonym: "TCECF" EXACT []
-is_a: XLMOD:06018 ! chloroformate reagent
-
-[Term]
-id: XLMOD:07037
-name: pentafluorobenzyl chloroformate
-def: "Pentafluorobenzyl chloroformate." [CAS:53526-74-2, PubChem_Compound:2775932, ChemSpiderID:2056259, ChemicalBookNo:CB8165220]
-synonym: "PFBCF" EXACT []
-is_a: XLMOD:06018 ! chloroformate reagent
-
-[Term]
-id: XLMOD:07038
-name: 1-chloroethyl chloroformate
-def: "1-chloroethyl chloroformate." [CAS:50893-53-3, PubChem_Compound:521305, ChemSpiderID:454726, ChemicalBookNo:CB5320341]
-synonym: "1CEF" EXACT []
-is_a: XLMOD:06018 ! chloroformate reagent
-
-[Term]
-id: XLMOD:07039
-name: N-Acetylimidazole
-def: "N-Acetylimidazole." [CAS:2466-76-4, PubChem_Compound:17174, ChemSpiderID:16257, ChemicalBookNo:CB9339608]
-synonym: "AIM" EXACT []
-is_a: XLMOD:06003 ! acylation reagent
-
-[Term]
-id: XLMOD:07040
-name: 1,3-Bis(chloromethyl)-1,1,3,3-tetramethyldisilazane
-def: "1,3-Bis(chloromethyl)-1,1,3,3-tetramethyldisilazane." [CAS:14579-91-0, PubChem_Compound:26740, ChemSpiderID:24914, ChemicalBookNo:CB1743876]
-synonym: "CMTMS" EXACT []
-is_a: XLMOD:06014 ! DMS reagent
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:07041
-name: Dimethylchlorosilane
-def: "Dimethylchlorosilane." [CAS:1066-35-9, PubChem_Compound:6327132, ChemSpiderID:59496, ChemicalBookNo:CB3694606]
-synonym: "DMCS" EXACT []
-is_a: XLMOD:06014 ! DMS reagent
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06510 ! ketone reactive
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:07042
-name: N-Trimethylsilylacetamide
-def: "N-Trimethylsilylacetamide." [CAS:13435-12-6, PubChem_Compound:25989, ChemSpiderID:24208, ChemicalBookNo:CB7667530]
-synonym: "TMSA" EXACT []
-synonym: "N-(Trimethylsilyl)acetamide" EXACT []
-is_a: XLMOD:06013 ! TMS reagent
-relationship: is_reactive_with XLMOD:06506 ! carbohydrate reactive
-
-[Term]
-id: XLMOD:07043
-name: N-(Trimethylsilyl)diethylamine
-def: "N-(Trimethylsilyl)diethylamine." [CAS:996-50-9, PubChem_Compound:70454, ChemSpiderID:63633, ChemicalBookNo:CB3771284]
-synonym: "TMSDEA" EXACT []
-is_a: XLMOD:06013 ! TMS reagent
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-
-[Term]
-id: XLMOD:07044
-name: trimethylphenylammonium hydroxide
-def: "Trimethylphenylammonium hydroxide." [CAS:1899-02-1, PubChem_Compound:15913, ChemSpiderID:15124, ChemicalBookNo:CB5316173]
-synonym: "TMPAH" EXACT []
-synonym: "MethElute reagent" EXACT []
-is_a: XLMOD:06002 ! alkylation reagent
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-relationship: is_reactive_with XLMOD:06502 ! amide reactive
-
-[Term]
-id: XLMOD:07045
-name: N,N-Dimethylformamidedimethyl acetal
-def: "N,N-Dimethylformamidedimethyl acetal." [CAS:4637-24-5, PubChem_Compound:78373, ChemSpiderID:70742, ChemicalBookNo:CB8178244]
-synonym: "DMFDMA" EXACT []
-synonym: "Methylate reagent" EXACT []
-is_a: XLMOD:06017 ! N,N-Dimethylformamidedialkyl acetal
-
-[Term]
-id: XLMOD:07046
-name: dimethyldichlorosilane
-def: "Dimethyldichlorosilane." [CAS:75-78-5, PubChem_Compound:6398, ChemSpiderID:6158, ChemicalBookNo:CB8854243]
-synonym: "DMDCS" EXACT []
-is_a: XLMOD:06014 ! DMS reagent
-
-[Term]
-id: XLMOD:07047
-name: N-t-Butyldimethylsilylimidazole
-def: "N-t-Butyldimethylsilylimidazole." [CAS:54925-64-3, PubChem_Compound:171385, ChemSpiderID:149827, ChemicalBookNo:CB1271225]
-synonym: "TBDMSIM" EXACT []
-is_a: XLMOD:06003 ! silylation reagent
-
-[Term]
-id: XLMOD:07048
-name: 4-Trimethylsiloxy-3-penten-2-one
-def: "4-Trimethylsiloxy-3-penten-2-one." [CAS:13257-81-3, PubChem_Compound:6059369, ChemSpiderID:4518416, ChemicalBookNo:CB3457672]
-is_a: XLMOD:06013 ! TMS reagent
-
-[Term]
-id: XLMOD:07049
-name: bromotrimethylsilane
-def: "Bromotrimethylsilane." [CAS:2857-97-8, PubChem_Compound:76113, ChemSpiderID:68599, ChemicalBookNo:CB9749809]
-is_a: XLMOD:06013 ! TMS reagent
-
-[Term]
-id: XLMOD:07050
-name: triisopropylsilyl chloride
-def: "Triisopropylsilyl chloride." [CAS:13154-24-0, PubChem_Compound:139400, ChemSpiderID:122926, ChemicalBookNo:CB3405310]
-is_a: XLMOD:06003 ! silylation reagent
-
-[Term]
-id: XLMOD:07051
-name: triisopropylsilyl trifluoromethanesulfonate
-def: "Triisopropylsilyl trifluoromethanesulfonate." [CAS:80522-42-5, PubChem_Compound:2724529, ChemSpiderID:2006662, ChemicalBookNo:CB5189874]
-is_a: XLMOD:06003 ! silylation reagent
-
-[Term]
-id: XLMOD:07052
-name: triethylsilyl trifluoromethanesulfonate
-def: "Triethylsilyl trifluoromethanesulfonate." [CAS:79271-56-0, PubChem_Compound:2733308, ChemSpiderID:2015110, ChemicalBookNo:CB6298346]
-is_a: XLMOD:06003 ! silylation reagent
-
-[Term]
-id: XLMOD:07053
-name: chlorotriethylsilane
-def: "Chlorotriethylsilane." [CAS:994-30-9, PubChem_Compound:13819, ChemSpiderID:13221, ChemicalBookNo:CB4746520]
-is_a: XLMOD:06003 ! silylation reagent
-
-[Term]
-id: XLMOD:07054
-name: chloro-dimethyl(pentafluorophenyl)silane
-def: "Chloro-dimethyl(pentafluorophenyl)silane." [CAS:20082-71-7, PubChem_Compound:88361, ChemSpiderID:79715, ChemicalBookNo:CB8853291]
-is_a: XLMOD:06003 ! silylation reagent
-
-[Term]
-id: XLMOD:07055
-name: N-Methyl-N-trimethylsilyl-heptafluorobutyramide
-def: "N-Methyl-N-trimethylsilyl-heptafluorobutyramide." [CAS:53296-64-3, PubChem_Compound:2775707, ChemSpiderID:2056039, ChemicalBookNo:CB1232811]
-synonym: "Mshfba" EXACT []
-is_a: XLMOD:06013 ! TMS reagent
-
-[Term]
-id: XLMOD:07056
-name: N-Methyl-N-trimethylsilylacetamide
-def: "N-Methyl-N-trimethylsilylacetamide." [CAS:7449-74-3, PubChem_Compound:81953, ChemSpiderID:73958, ChemicalBookNo:CB4355232]
-is_a: XLMOD:06013 ! TMS reagent
-
-[Term]
-id: XLMOD:07057
-name: hexamethyldisiloxane
-def: "Hexamethyldisiloxane." [CAS:107-46-0, PubChem_Compound:24764, ChemSpiderID:23150, ChemicalBookNo:CB2446352]
-is_a: XLMOD:06003 ! silylation reagent
-
-[Term]
-id: XLMOD:07058
-name: 1,1,3,3-Tetramethyl-1,3-diphenyldisilazane
-def: "1,1,3,3-Tetramethyl-1,3-diphenyldisilazane." [CAS:3449-26-1, PubChem_Compound:76988, ChemSpiderID:69434, ChemicalBookNo:CB7212822]
-is_a: XLMOD:06003 ! silylation reagent
-
-[Term]
-id: XLMOD:07059
-name: N,N-Dimethyltrimethylsilylamine
-def: "N,N-Dimethyltrimethylsilylamine." [CAS:2083-91-2, PubChem_Compound:74965, ChemSpiderID:67521, ChemicalBookNo:CB1279847]
-is_a: XLMOD:06013 ! TMS reagent
-
-[Term]
-id: XLMOD:07060
-name: N,N'-Bis(trimethylsilyl)urea
-def: "N,N'-Bis(trimethylsilyl)urea." [CAS:18297-63-7, PubChem_Compound:87562, ChemSpiderID:78992, ChemicalBookNo:CB6152161]
-is_a: XLMOD:06013 ! TMS reagent
-
-[Term]
-id: XLMOD:07061
-name: N,O-Bis(trimethylsilyl)carbamate
-def: "N,O-Bis(trimethylsilyl)carbamate." [CAS:35342-88-2, PubChem_Compound:3015764, ChemSpiderID:2283833, ChemicalBookNo:CB2248969]
-is_a: XLMOD:06013 ! TMS reagent
-
-[Term]
-id: XLMOD:07062
-name: N,N-Bis(trimethylsilyl)methylamine
-def: "N,N-Bis(trimethylsilyl)methylamine." [CAS:920-68-3, PubChem_Compound:70199, ChemSpiderID:63385, ChemicalBookNo:CB0439806]
-is_a: XLMOD:06013 ! TMS reagent
-
-[Term]
-id: XLMOD:07063
-name: bis(dimethylamino)dimethylsilane
-def: "Bis(dimethylamino)dimethylsilane." [CAS:3768-58-9, PubChem_Compound:77384, ChemSpiderID:69798, ChemicalBookNo:CB1214899]
-is_a: XLMOD:06003 ! silylation reagent
-
-[Term]
-id: XLMOD:07064
-name: Trimethylsilyl methallylsulfinate
-def: "Trimethylsilyl methallylsulfinate." [CAS:723336-86-5, PubChem_Compound:71312539, ChemSpiderID:28419285, ChemicalBookNo:CB32750948]
-is_a: XLMOD:06013 ! TMS reagent
-
-[Term]
-id: XLMOD:07065
-name: Triethylsilyl methallylsulfinate
-def: "Triethylsilyl methallylsulfinate." [CAS:850418-19-8, PubChem_Compound:71312540, ChemSpiderID:35789839, ChemicalBookNo:CB42756013]
-is_a: XLMOD:06003 ! silylation reagent
-
-[Term]
-id: XLMOD:07066
-name: tert-Butyldimethylsilyl methallylsulfinate
-def: "Tert-Butyldimethylsilyl methallylsulfinate." [CAS:850418-20-1, PubChem_Compound:71312541, ChemSpiderID:35789840, ChemicalBookNo:CB72750946]
-synonym: "SILMAS-TBS" EXACT []
-is_a: XLMOD:06003 ! silylation reagent
-
-[Term]
-id: XLMOD:07067
-name: methyltrifluoromethanesulfonate
-def: "Methyltrifluoromethanesulfonate." [CAS:333-27-7, PubChem_Compound:9526, ChemSpiderID:9153, ChemicalBookNo:CB9131563]
-is_a: XLMOD:06004 ! acylation reagent
-
-[Term]
-id: XLMOD:07068
-name: ethyl trifluoromethanesulfonate
-def: "Ethyl trifluoromethanesulfonate." [CAS:425-75-2, PubChem_Compound:67924, ChemSpiderID:61241, ChemicalBookNo:CB4332659]
-is_a: XLMOD:06004 ! acylation reagent
-
-[Term]
-id: XLMOD:07069
-name: trichloroacetyl chloride
-def: "Trichloroacetyl chloride." [CAS:76-02-8, PubChem_Compound:6420, ChemSpiderID:6180, ChemicalBookNo:CB6854254]
-is_a: XLMOD:06004 ! acylation reagent
-
-[Term]
-id: XLMOD:07070
-name: 2-Thenoyltrifluoroacetone
-def: "2-Thenoyltrifluoroacetone." [CAS:326-91-0, PubChem_Compound:5601, ChemSpiderID:5399, ChemicalBookNo:CB3219722]
-is_a: XLMOD:06004 ! acylation reagent
-
-[Term]
-id: XLMOD:07071
-name: 2,2,6,6-Tetramethyl-3,5-heptanedione
-def: "2,2,6,6-Tetramethyl-3,5-heptanedione." [CAS:1118-71-4, PubChem_Compound:70700, ChemSpiderID:63866, ChemicalBookNo:CB1373637]
-is_a: XLMOD:06004 ! acylation reagent
-
-[Term]
-id: XLMOD:07072
-name: N-Methyl-bis-heptafluorobutyramide
-def: "N-Methyl-bis-heptafluorobutyramide." [CAS:73980-71-9, PubChem_Compound:597974, ChemSpiderID:519801, ChemicalBookNo:CB6699309]
-is_a: XLMOD:06004 ! acylation reagent
-
-[Term]
-id: XLMOD:07073
-name: N,N'-Diisopropyl-O-methylisourea
-def: "N,N'-Diisopropyl-O-methylisourea." [CAS:54648-79-2, PubChem_Compound:383824, ChemSpiderID:340092, ChemicalBookNo:CB4130844]
-is_a: XLMOD:06004 ! acylation reagent
-
-[Term]
-id: XLMOD:07074
-name: 3,3,3-Trifluoro-2-methoxy-2-phenylpropanoic acid
-def: "3,3,3-Trifluoro-2-methoxy-2-phenylpropanoic acid." [CAS:81655-41-6, PubChem_Compound:86531, ChemSpiderID:5360910, ChemicalBookNo:CB4264981]
-is_a: XLMOD:06004 ! acylation reagent
-
-[Term]
-id: XLMOD:07075
-name: 6,6,7,7,8,8,8-Heptafluoro-2,2-dimethyl-3,5-octanedione
-def: "6,6,7,7,8,8,8-Heptafluoro-2,2-dimethyl-3,5-octanedione." [CAS:17587-22-3, PubChem_Compound:28614, ChemSpiderID:26612, ChemicalBookNo:CB2271873]
-is_a: XLMOD:06004 ! acylation reagent
-
-[Term]
-id: XLMOD:07076
-name: 4-Bromophenacyl trifluoro-methanesulfonate
-def: "4-Bromophenacyl trifluoro-methanesulfonate." [CAS:93128-04-2, PubChem_Compound:125008, ChemSpiderID:111291, ChemicalBookNo:CB4137500]
-synonym: "4-Bromophenacyl triflate" EXACT []
-is_a: XLMOD:06004 ! acylation reagent
-relationship: has_fluorophore XLMOD:06111 ! 4-bromophenacyl
-
-[Term]
-id: XLMOD:07077
-name: 2,3-Diaminotoluene
-def: "2,3-Diaminotoluene." [CAS:2687-25-4, PubChem_Compound:17593, ChemSpiderID:16633, ChemicalBookNo:CB2736932]
-is_a: XLMOD:06004 ! acylation reagent
-
-[Term]
-id: XLMOD:07078
-name: 2,6-Diamino-4-pyrimidinone
-def: "2,6-Diamino-4-pyrimidinone." [CAS:56-06-4, PubChem_Compound:2944, ChemSpiderID:2840, ChemicalBookNo:CB0174912]
-is_a: XLMOD:06004 ! acylation reagent
-
-[Term]
-id: XLMOD:07079
-name: benzoic acid
-def: "Benzoic acid." [CAS:65-85-0, PubChem_Compound:243, ChemSpiderID:238, ChemicalBookNo:CB8698780]
-is_a: XLMOD:06004 ! acylation reagent
-
-[Term]
-id: XLMOD:07080
-name: tert-Butyl methyl ether
-def: "Tert-Butyl methyl ether." [CAS:1634-04-4, PubChem_Compound:15413, ChemSpiderID:14672, ChemicalBookNo:CB2853178]
-is_a: XLMOD:06004 ! acylation reagent
-
-[Term]
-id: XLMOD:07081
-name: ethyl acetoacetate
-def: "Ethyl acetoacetate." [CAS:141-97-9, PubChem_Compound:8868, ChemSpiderID:13865426, ChemicalBookNo:CB0301721]
-is_a: XLMOD:06004 ! acylation reagent
-
-[Term]
-id: XLMOD:07082
-name: (1S)-(+)-Menthyl chloroformate
-def: "(1S)-(+)-Menthyl chloroformate." [CAS:7635-54-3, PubChem_Compound:2733329, ChemSpiderID:2015131, ChemicalBookNo:CB5397503]
-is_a: XLMOD:06004 ! acylation reagent
-is_a: XLMOD:06009 ! chiral derivatization reagent
-is_a: XLMOD:06018 ! chloroformate reagent
-
-[Term]
-id: XLMOD:07083
-name: butylboronic acid
-def: "Butylboronic acid." [CAS:4426-47-5, PubChem_Compound:20479, ChemSpiderID:19286, ChemicalBookNo:CB6431756]
-is_a: XLMOD:06004 ! acylation reagent
-relationship: has_reactive_group XLMOD:00161 ! boronic acid
-
-[Term]
-id: XLMOD:07084
-name: 1-(Pentafluoropropionyl) imidazole
-def: "1-(Pentafluoropropionyl) imidazole." [CAS:71735-32-5, PubChem_Compound:100821, ChemSpiderID:91097, ChemicalBookNo:CB8441122]
-is_a: XLMOD:06004 ! acylation reagent
-
-[Term]
-id: XLMOD:07085
-name: hexafluoroacetylacetone
-def: "Hexafluoroacetylacetone." [CAS:1522-22-1, PubChem_Compound:73706, ChemSpiderID:21106446, ChemicalBookNo:CB8188414]
-synonym: "Hexafluoro-2,4-pentanedione" EXACT []
-is_a: XLMOD:06004 ! acylation reagent
-
-[Term]
-id: XLMOD:07086
-name: 2,3,4,5,6-Pentafluorobenzaldehyde
-def: "2,3,4,5,6-Pentafluorobenzaldehyde." [CAS:653-37-2, PubChem_Compound:69558, ChemSpiderID:21106527, ChemicalBookNo:CB6754598]
-is_a: XLMOD:06004 ! acylation reagent
-
-[Term]
-id: XLMOD:07087
-name: pentafluorobenzenesulfonyl chloride
-def: "Pentafluorobenzenesulfonyl chloride." [CAS:832-53-1, PubChem_Compound:70026, ChemSpiderID:63216, ChemicalBookNo:CB7243712]
-is_a: XLMOD:06004 ! acylation reagent
-
-[Term]
-id: XLMOD:07088
-name: 1,1,1-Trifluoro-2,4-pentanedione
-def: "1,1,1-Trifluoro-2,4-pentanedione." [CAS:367-57-7, PubChem_Compound:73943, ChemSpiderID:66573, ChemicalBookNo:CB6699233]
-is_a: XLMOD:06015 ! TFA reagent
-
-[Term]
-id: XLMOD:07089
-name: 1,1,1-Trifluoroacetone
-def: "1,1,1-Trifluoroacetone." [CAS:421-50-1, PubChem_Compound:9871, ChemSpiderID:21111803, ChemicalBookNo:CB4123453]
-is_a: XLMOD:06015 ! TFA reagent
-
-[Term]
-id: XLMOD:07090
-name: 4-(Trifluoromethyl)benzoyl chloride
-def: "4-(Trifluoromethyl)benzoyl chloride." [CAS:329-15-7, PubChem_Compound:67607, ChemSpiderID:60927, ChemicalBookNo:CB9762316]
-is_a: XLMOD:06015 ! TFA reagent
-
-[Term]
-id: XLMOD:07091
-name: 8-Quinolinesulfonyl chloride
-def: "8-Quinolinesulfonyl chloride." [CAS:18704-37-5, PubChem_Compound:29220, ChemSpiderID:27177, ChemicalBookNo:CB8329163]
-is_a: XLMOD:06004 ! acylation reagent
-
-[Term]
-id: XLMOD:07092
-name: (1R)-(-)-Menthyl chloroformate
-def: "(1R)-(-)-Menthyl chloroformate." [CAS:14602-86-9, PubChem_Compound:7014897, ChemSpiderID:17206727, ChemicalBookNo:CB7248919]
-is_a: XLMOD:06004 ! acylation reagent
-is_a: XLMOD:06009 ! chiral derivatization reagent
-is_a: XLMOD:06018 ! chloroformate reagent
-
-[Term]
-id: XLMOD:07093
-name: phenylboronic acid
-def: "Phenylboronic acid." [CAS:98-80-6, PubChem_Compound:66827, ChemSpiderID:60191, ChemicalBookNo:CB5323625]
-is_a: XLMOD:06004 ! acylation reagent
-relationship: has_reactive_group XLMOD:00161 ! boronic acid
-
-[Term]
-id: XLMOD:07094
-name: methylboronic acid
-def: "Methylboronic acid." [CAS:13061-96-6, PubChem_Compound:139377, ChemSpiderID:122904, ChemicalBookNo:CB3373202]
-is_a: XLMOD:06004 ! acylation reagent
-relationship: has_reactive_group XLMOD:00161 ! boronic acid
-
-[Term]
-id: XLMOD:07095
-name: 2,3,4,5,6-Pentafluorobenzoic anhydride
-def: "2,3,4,5,6-Pentafluorobenzoic anhydride." [CAS:15989-99-8, PubChem_Compound:189034, ChemSpiderID:164254, ChemicalBookNo:CB3497119]
-is_a: XLMOD:06004 ! acylation reagent
-
-[Term]
-id: XLMOD:07096
-name: 4-(Dimethylamino)benzoyl chloride
-def: "4-(Dimethylamino)benzoyl chloride." [CAS:4755-50-4, PubChem_Compound:4400782, ChemSpiderID:3601987, ChemicalBookNo:CB6399872]
-is_a: XLMOD:06004 ! acylation reagent
-
-[Term]
-id: XLMOD:07097
-name: boron trifluoride butanol
-def: "Boron trifluoride butanol." [CAS:7637-07-2, PubChem_Compound:6356, ChemSpiderID:6116, ChemicalBookNo:CB3238105]
-synonym: "BF3-butanol" EXACT []
-is_a: XLMOD:06016 ! boron trifluoride reagent
-
-[Term]
-id: XLMOD:07098
-name: 1,1,1,3,3,3-Hexafluoro-2-propanol
-def: "1,1,1,3,3,3-Hexafluoro-2-propanol." [CAS:920-66-1, PubChem_Compound:13529, ChemSpiderID:10606755, ChemicalBookNo:CB3251829]
-is_a: XLMOD:06002 ! alkylation reagent
-
-[Term]
-id: XLMOD:07099
-name: 2,2,3,3,3-Pentafluoro-1-propanol
-def: "2,2,3,3,3-Pentafluoro-1-propanol." [CAS:422-05-9, PubChem_Compound:9872, ChemSpiderID:9488, ChemicalBookNo:CB9689963]
-is_a: XLMOD:06002 ! alkylation reagent
-
-[Term]
-id: XLMOD:07100
-name: 2,3,5,6-Tetrafluoro-4-ethanol(trifluoromethyl)benzyl bromide
-def: "2,3,5,6-Tetrafluoro-4-ethanol(trifluoromethyl)benzyl bromide." [CAS:76437-40-6, PubChem_Compound:127137, ChemSpiderID:112859, ChemicalBookNo:CB1682115]
-is_a: XLMOD:06002 ! alkylation reagent
-relationship: has_reactive_group XLMOD:00168 ! benzyl bromide reactive group
-
-[Term]
-id: XLMOD:07101
-name: 2,3-Dihydroxy-biphenyl
-def: "2,3-Dihydroxy-biphenyl." [CAS:1133-63-7, PubChem_Compound:254, ChemSpiderID:249, ChemicalBookNo:CB0302647]
-is_a: XLMOD:06002 ! alkylation reagent
-
-[Term]
-id: XLMOD:07102
-name: O-(2,3,4,5,6-Pentafluorobenzyl)hydroxylamine hydrochloride
-def: "O-(2,3,4,5,6-Pentafluorobenzyl)hydroxylamine hydrochloride." [CAS:57981-02-9, PubChem_Compound:122307, ChemSpiderID:109062, ChemicalBookNo:CB8307815]
-synonym: "Florox reagent" EXACT []
-is_a: XLMOD:06002 ! alkylation reagent
-
-[Term]
-id: XLMOD:07103
-name: pentafluoroiodoethane
-def: "Pentafluoroiodoethane." [CAS:354-64-3, PubChem_Compound:9636, ChemSpiderID:9259, ChemicalBookNo:CB1226715]
-is_a: XLMOD:06002 ! alkylation reagent
-
-[Term]
-id: XLMOD:07104
-name: tetrabutylammoniumtetrabutylborate
-def: "Tetrabutylammoniumtetrabutylborate." [CAS:23231-91-6, PubChem_Compound:11123692, ChemSpiderID:9298821, ChemicalBookNo:CB9765711]
-is_a: XLMOD:06002 ! alkylation reagent
-
-[Term]
-id: XLMOD:07105
-name: trimethylboroxine
-def: "Trimethylboroxine." [CAS:823-96-1, PubChem_Compound:574072, ChemSpiderID:499140, ChemicalBookNo:499140]
-is_a: XLMOD:06002 ! alkylation reagent
-
-[Term]
-id: XLMOD:07107
-name: boron trifluoride propanol
-def: "Boron trifluoride propanol." [CAS:762-48-1, ChemSpiderID:11428571, ChemicalBookNo:CB7289428]
-synonym: "BF3-propanol" EXACT []
-is_a: XLMOD:06016 ! boron trifluoride reagent
-
-[Term]
-id: XLMOD:07108
-name: 4-Bromobenzyl bromide
-def: "4-Bromobenzyl bromide." [CAS:589-15-1, PubChem_Compound:68527, ChemSpiderID:61802, ChemicalBookNo:CB8313784]
-is_a: XLMOD:06020 ! arylation reagent
-relationship: has_reactive_group XLMOD:00168 ! benzyl bromide reactive group
-
-[Term]
-id: XLMOD:07109
-name: N,N-Dimethylformamidediethyl acetal
-def: "N,N-Dimethylformamidediethyl acetal." [CAS:1188-33-6, PubChem_Compound:70913, ChemSpiderID:64076, ChemicalBookNo:CB6665913]
-synonym: "1,1-Diethoxy-N,N-dimethylmethanamine" EXACT []
-is_a: XLMOD:06017 ! N,N-Dimethylformamidedialkyl acetal
-
-[Term]
-id: XLMOD:07110
-name: N,N-Dimethylformamidedibutyl acetal
-def: "N,N-Dimethylformamidedibutyl acetal." [CAS:18503-90-7, PubChem_Compound:87683, ChemSpiderID:79103, ChemicalBookNo:CB8770217]
-synonym: "1,1-Dibutoxy-N,N-dimethylmethanamine" EXACT []
-is_a: XLMOD:06017 ! N,N-Dimethylformamidedialkyl acetal
-
-[Term]
-id: XLMOD:07111
-name: N,N-Dimethylformamidediisopropyl acetal
-def: "N,N-Dimethylformamidediisopropyl acetal." [CAS:18503-89-4, PubChem_Compound:87682, ChemSpiderID:79102, ChemicalBookNo:CB1137822]
-is_a: XLMOD:06017 ! N,N-Dimethylformamidedialkyl acetal
-
-[Term]
-id: XLMOD:07112
-name: N,N-Dimethylformamidedineopentyl acetal
-def: "N,N-Dimethylformamidedineopentyl acetal." [CAS:4909-78-8, PubChem_Compound:78623, ChemSpiderID:70980, ChemicalBookNo:CB1335538]
-is_a: XLMOD:06017 ! N,N-Dimethylformamidedialkyl acetal
-
-[Term]
-id: XLMOD:07113
-name: N,N-Dimethylformamidedipropyl acetal
-def: "N,N-Dimethylformamidedipropyl acetal." [CAS:6006-65-1, PubChem_Compound:80105, ChemSpiderID:72355, ChemicalBookNo:CB4137823]
-is_a: XLMOD:06017 ! N,N-Dimethylformamidedialkyl acetal
-
-[Term]
-id: XLMOD:07114
-name: N,N-Dimethylformamidedi-tert-butyl acetal
-def: "N,N-Dimethylformamidedi-tert-butyl acetal." [CAS:36805-97-7, PubChem_Compound:547712, ChemSpiderID:476708, ChemicalBookNo:CB5296219]
-is_a: XLMOD:06017 ! N,N-Dimethylformamidedialkyl acetal
-
-[Term]
-id: XLMOD:07115
-name: nonafluoro-1-iodobutane
-def: "Nonafluoro-1-iodobutane." [CAS:423-39-2, PubChem_Compound:67917, ChemSpiderID:61234, ChemicalBookNo:CB9474482]
-synonym: "Perfluorobutyl iodide" EXACT []
-synonym: "1-Iodoperfluorobutane" EXACT []
-is_a: XLMOD:06002 ! alkylation reagent
-
-[Term]
-id: XLMOD:07116
-name: triethyloxonium tetrafluoroborate
-def: "Triethyloxonium tetrafluoroborate." [CAS:368-39-8, PubChem_Compound:2723982, ChemSpiderID:2006158, ChemicalBookNo:CB0198800]
-is_a: XLMOD:06019 ! trialkyloxonium reagent
-
-[Term]
-id: XLMOD:07117
-name: 2,2,2-Trichloroethanol
-def: "2,2,2-Trichloroethanol." [CAS:115-20-8, PubChem_Compound:8259, ChemSpiderID:7961, ChemicalBookNo:CB7257753]
-is_a: XLMOD:06002 ! alkylation reagent
-
-[Term]
-id: XLMOD:07118
-name: triethyloxonium hexafluorophosphate
-def: "Triethyloxonium hexafluorophosphate." [CAS:17950-40-2, PubChem_Compound:167684, ChemSpiderID:146692, ChemicalBookNo:CB4151711]
-is_a: XLMOD:06019 ! trialkyloxonium reagent
-
-[Term]
-id: XLMOD:07119
-name: 2,2,2-Trifluoroethanol
-def: "2,2,2-Trifluoroethanol." [CAS:75-89-8, PubChem_Compound:6409, ChemSpiderID:21106169, ChemicalBookNo:CB5736665]
-is_a: XLMOD:06002 ! alkylation reagent
-
-[Term]
-id: XLMOD:07120
-name: trimethyloxonium tetrafluoroborate
-def: "Trimethyloxonium tetrafluoroborate." [CAS:420-37-1, PubChem_Compound:2735153, ChemSpiderID:2016863, ChemicalBookNo:CB3184284]
-is_a: XLMOD:06019 ! trialkyloxonium reagent
-
-[Term]
-id: XLMOD:07121
-name: 2,2-Dimethoxypropane
-def: "2,2-Dimethoxypropane." [CAS:77-76-9, PubChem_Compound:6495, ChemSpiderID:21106033, ChemicalBookNo:CB9373512]
-is_a: XLMOD:06002 ! alkylation reagent
-
-[Term]
-id: XLMOD:07122
-name: 4-Tolylsulfonylmethylnitrosamide
-def: "4-Tolylsulfonylmethylnitrosamide." [CAS:80-11-5, PubChem_Compound:6628, ChemSpiderID:6376, ChemicalBookNo:CB7663729]
-synonym: "Diazald" EXACT []
-synonym: "N-Methyl-N-nitrosotoluene-4-sulphonamide" EXACT []
-is_a: XLMOD:06002 ! alkylation reagent
-
-[Term]
-id: XLMOD:07123
-name: 18-Crown-6
-def: "18-Crown-6." [CAS:17455-13-9, PubChem_Compound:28557, ChemSpiderID:26563, ChemicalBookNo:CB4445218]
-is_a: XLMOD:06002 ! alkylation reagent
-
-[Term]
-id: XLMOD:07124
-name: 3-Aminopropyltriethoxysilane
-def: "3-Aminopropyltriethoxysilane." [CAS:919-30-2, PubChem_Compound:13521, ChemSpiderID:12933, ChemicalBookNo:CB8686147]
-synonym: "APTES" EXACT []
-is_a: XLMOD:06003 ! silylation reagent
-
-[Term]
-id: XLMOD:09000
-name: dansyl chloride
-def: "Dansyl chloride." [CAS:605-65-2, PubChem_Compound:14513518, ChemSpiderID:11308, ChemicalBookNo:CB5696240, PMID:23524938]
-synonym: "DNS-Cl" EXACT []
-synonym: "5-dimethylamino-1-naphthalenesulfonyl chloride" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00156 ! sulfonyl chloride
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-relationship: is_reactive_with XLMOD:06515 ! nucleoside reactive
-
-[Term]
-id: XLMOD:09001
-name: picolinic acid
-def: "Picolinic acid." [CAS:98-98-6, PubChem_Compound:1018, ChemSpiderID:993, ChemicalBookNo:CB8196640, PMID:23524938]
-synonym: "PA" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06509 ! phenol reactive
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:09002
-name: fusaric acid
-def: "Fusaric acid." [CAS:536-69-6, PubChem_Compound:3442, ChemSpiderID:3324, ChemicalBookNo:CB4689029, PMID:23524938]
-synonym: "FA" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06509 ! phenol reactive
-
-[Term]
-id: XLMOD:09003
-name: dimethylglycine
-def: "Dimethylglycine." [CAS:1118-68-9, PubChem_Compound:673, ChemSpiderID:653, ChemicalBookNo:1118-68-9, PMID:23524938]
-synonym: "N,N-Dimethylglycine" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06509 ! phenol reactive
-
-[Term]
-id: XLMOD:09004
-name: isonicotinoyl azide
-def: "Isonicotinoyl azide." [PubChem_Compound:11701058, ChemSpiderID:9875783, ChemicalBookNo:CB1385038, PMID:23524938, PMID:26454158]
-synonym: "INA" EXACT []
-synonym: "Pyridine-4-carbonyl azide" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06509 ! phenol reactive
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:09005
-name: NA-NHS ester
-def: "N-hydroxysuccinimide esters of N-alkyl(C1-C4)nicotinic acids." [PMID:16808485, PMID:22575224]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-
-[Term]
-id: XLMOD:09006
-name: 2-fluoro-1-methylpyridinium p-toluenesulfonate
-def: "2-fluoro-1-methylpyridinium p-toluenesulfonate." [CAS:58086-67-2, ChemSpiderID:150036, ChemicalBookNo:CB1142305, PMID:23524938]
-synonym: "FMP" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00165 ! sulfonate
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06509 ! phenol reactive
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:09007
-name: 3-nitrophthalic anhydride
-def: "3-nitrophthalic anhydride." [CAS:641-70-3, PubChem_Compound:21631, ChemSpiderID:20330, ChemicalBookNo:CB8116378, PMID:7802865, PMID:23524938]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00166 ! anhydride
-
-[Term]
-id: XLMOD:09008
-name: 2-hydrazino-1-methylpyridine
-def: "2-hydrazino-1-methylpyridine." [ChemSpiderID:21376238, PMID:23524938]
-synonym: "HMP" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00159 ! hydrazine
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:09009
-name: 2-hydrazinopyridine
-def: "2-hydrazinopyridine." [CAS:4930-98-7, PubChem_Compound:78645, ChemSpiderID:71000, ChemicalBookNo:CB0389206, PMID:23524938, PMID:26454158]
-synonym: "HP" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00159 ! hydrazine
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:09010
-name: dansyl hydrazine
-def: "Dansyl hydrazine." [CAS:33008-06-9, PubChem_Compound:94442, ChemSpiderID:85229, ChemicalBookNo:CB9236754, PMID:23524938]
-synonym: "Dns-Hz" EXACT []
-synonym: "DH" EXACT []
-synonym: "5-dimethylaminonaphthalene-1-sulfonyl hydrazine" EXACT []
-synonym: "5-(Dimethylamino)-1-naphthalenesulfonohydrazide" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00159 ! hydrazine
-
-[Term]
-id: XLMOD:09011
-name: Girard's reagent P
-def: "Pyridinioacetohydrazide chloride." [CAS:1126-58-5, PubChem_Compound:70773, ChemSpiderID:63938, ChemicalBookNo:CB2285753, PMID:23524938]
-synonym: "Gir P" EXACT []
-synonym: "GP" EXACT []
-synonym: "1-(carboxymethyl)pyridium chloride hydrazide" EXACT []
-synonym: "1-(2-hydrazino-2-oxoethyl)pyridinium chloride" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00110 ! hydrazide
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:09012
-name: Girard's reagent T
-def: "Betaine Hydrazide Hydrochloride." [CAS:123-46-6, PubChem_Compound:67156, ChemSpiderID:60501, ChemicalBookNo:CB9414297, PMID:23524938]
-synonym: "Gir T" EXACT []
-synonym: "GT" EXACT []
-synonym: "1-(carboxymethyl)trimethylammonium chloride hydrazide" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00110 ! hydrazide
-relationship: is_reactive_with XLMOD:06515 ! nucleoside reactive
-
-[Term]
-id: XLMOD:09013
-name: 2,4-dinitrophenylhydrazine
-def: "2,4-dinitrophenylhydrazine." [CAS:119-26-6, PubChem_Compound:3772977, ChemSpiderID:3001507, ChemicalBookNo:CB4852908, PMID:23524938]
-synonym: "DNPH" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_fluorophore XLMOD:06104 ! 2,4-dinitrophenyl
-relationship: has_reactive_group XLMOD:00159 ! hydrazine
-
-[Term]
-id: XLMOD:09014
-name: hydroxylamine
-def: "Hydroxylamine." [CAS:7803-49-8, PubChem_Compound:787, ChemSpiderID:766, ChemicalBookNo:CB3345090, PMID:23524938]
-synonym: "HA" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00133 ! amine reactive group
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-relationship: is_reactive_with XLMOD:00031 ! aldehyde reactive
-relationship: is_reactive_with XLMOD:06510 ! ketone reactive
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:09015
-name: 4-[2-(Trimethylammonio)ethoxy]anilinium dibromide
-def: "4-[2-(Trimethylammonio)ethoxy]anilinium dibromide." [CAS:1076196-38-7, ChemSpiderID:29342342, ChemicalBookNo:CB32747247, PMID:23524938]
-synonym: "4-APC" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00031 ! aldehyde reactive
-relationship: is_reactive_with XLMOD:06510 ! ketone reactive
-
-[Term]
-id: XLMOD:09016
-name: 4-(2-((4-bromophenethyl)dimethylammonio)ethoxy)benzenaminium dibromide
-def: "4-(2-((4-bromophenethyl)dimethylammonio)ethoxy)benzenaminium dibromide." [CAS:197305-97-8, PubChem_Compound:91826487, ChemSpiderID:1064766, ChemicalBookNo:CB7444959, PMID:23524938]
-synonym: "4-APEBA" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-relationship: is_reactive_with XLMOD:00031 ! aldehyde reactive
-relationship: is_reactive_with XLMOD:06510 ! ketone reactive
-
-[Term]
-id: XLMOD:09017
-name: D-Cysteine
-def: "D-Cysteine." [CAS:921-01-7, PubChem_Compound:92851, ChemSpiderID:83819, ChemicalBookNo:CB4407452, PMID:23524938]
-is_a: XLMOD:06009 ! chiral derivatization reagent
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00031 ! aldehyde reactive
-relationship: is_reactive_with XLMOD:06510 ! ketone reactive
-
-[Term]
-id: XLMOD:09018
-name: 2-Picolylamine
-def: "2-Picolylamine." [CAS:3731-51-9, PubChem_Compound:19509, ChemSpiderID:18383, ChemicalBookNo:CB8853569, PMID:23524938]
-synonym: "2-PA" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09019
-name: 3-Picolylamine
-def: "3-Picolylamine." [CAS:3731-52-0, PubChem_Compound:31018, ChemSpiderID:28777, ChemicalBookNo:CB2284635, PMID:23524938]
-synonym: "3-PA" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09020
-name: 3-picolylcarbinol
-def: "3-picolylcarbinol." [ChemSpiderID:72714, PMID:23524938]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09021
-name: 3-Hydroxy-1-methyl-piperidine
-def: "3-Hydroxy-1-methyl-piperidine." [CAS:3554-74-3, PubChem_Compound:98016, ChemSpiderID:88489, ChemicalBookNo:CB7340664, PMID:23524938]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09022
-name: 3-(Hydroxymethyl)-pyridine
-def: "3-(Hydroxymethyl)-pyridine." [CAS:100-55-0, PubChem_Compound:7510, ChemSpiderID:7229, ChemicalBookNo:CB6384809, PMID:23524938]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09023
-name: 4-Diazomethylpyridine
-def: "4-Diazomethylpyridine." [CAS:26363-69-9, PubChem_Compound:12066686, ChemSpiderID:57445102, PMID:23524938]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09024
-name: 4-[2-(N,Ndimethylamino)ethylaminosulfonyl]-7-(2-aminoethylamino)-2,1,3-benzoxadiazole
-def: "4-[2-(N,Ndimethylamino)ethylaminosulfonyl]-7-(2-aminoethylamino)-2,1,3-benzoxadiazole." [CAS:913253-56-2, PubChem_Compound:91247932, ChemSpiderID:21377953, ChemicalBookNo:CB62720627, PMID:23524938]
-synonym: "DAABD-AE" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00157 ! benzofurazan
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-
-[Term]
-id: XLMOD:09025
-name: 1-Butanol hydrochloride
-def: "1-Butanol hydrochloride." [ChemSpiderID:13206062, PMID:23524938]
-synonym: "Butanol + HCl" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09026
-name: fluorenylmethyloxycarbonyl chloride
-def: "Fluorenylmethyloxycarbonyl chloride." [CAS:28920-43-6, PubChem_Compound:34367, ChemSpiderID:31647, ChemicalBookNo:CB7234569, PMID:23524938]
-synonym: "FMOC-Cl" EXACT []
-synonym: "1-(9-Fluorenyl)methyl chloroformate" EXACT []
-is_a: XLMOD:06018 ! chloroformate reagent
-
-[Term]
-id: XLMOD:09027
-name: N-Methyl-2-phenylethanamide
-def: "N-Methyl-2-phenylethanamide." [CAS:6830-82-6, PubChem_Compound:81274, ChemSpiderID:73329, ChemicalBookNo:CB4717700, PMID:23524938]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09028
-name: 2-Bromo-1-(4-(dimethylamino)phenyl)ethanone
-def: "2-Bromo-1-(4-(dimethylamino)phenyl)ethanone." [CAS:37904-72-6, PubChem_Compound:142225, ChemSpiderID:125460, ChemicalBookNo:CB4113692, PMID:23524938]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09029
-name: 6-aminoquinolyl-N-hydroxysuccinimidyl carbamate
-def: "6-aminoquinolyl-N-hydroxysuccinimidyl carbamate." [ChemSpiderID:2043270, PMID:23524938, PMID:16384748]
-synonym: "6-ACQ" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00164 ! carbamate
-
-[Term]
-id: XLMOD:09030
-name: 3-Pyridyl isothiocyanate
-def: "3-Pyridyl isothiocyanate." [CAS:17452-27-6, PubChem_Compound:2737242, ChemSpiderID:2018885, ChemicalBookNo:CB4371720, PMID:23524938]
-synonym: "3-Isothiocyanatopyridine" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00162 ! isothiocyanate
-
-[Term]
-id: XLMOD:09031
-name: phenyl isothiocyanate
-def: "Phenyl isothiocyanate." [CAS:103-72-0, PubChem_Compound:7673, ChemSpiderID:7390, ChemicalBookNo:CB5733806, PMID:23524938, PMID:26496130]
-synonym: "PITC" EXACT []
-synonym: "Edman's reagent" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00162 ! isothiocyanate
-
-[Term]
-id: XLMOD:09032
-name: isobutyl chloroformate
-def: "Isobutyl chloroformate." [CAS:543-27-1, PubChem_Compound:62365, ChemSpiderID:56154, ChemicalBookNo:CB7165612, PMID:23524938]
-synonym: "IBCF" EXACT []
-synonym: "i-BuCF" EXACT []
-is_a: XLMOD:06018 ! chloroformate reagent
-relationship: is_reactive_with XLMOD:06511 ! biphosphonate drug reactive
-
-[Term]
-id: XLMOD:09033
-name: 4-(N,N-Dimethylaminosulfonyl)-7-fluoro-2,1,3-benzoxadiazole
-def: "4-(N,N-Dimethylaminosulfonyl)-7-fluoro-2,1,3-benzoxadiazole." [CAS:98358-90-8, PubChem_Compound:126917, ChemSpiderID:112705, ChemicalBookNo:CB3366336, PMID:23524938, PMID:27582321]
-synonym: "DBD-F" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_property XLMOD:00015 ! fluorescent
-relationship: has_reactive_group XLMOD:00158 ! halobenzofurazan
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:06513 ! thiol reactive
-
-[Term]
-id: XLMOD:09034
-name: 4-Bromophenacyl bromide
-def: "4-Bromophenacyl bromide." [CAS:99-73-0, PubChem_Compound:7454, ChemSpiderID:7174, ChemicalBookNo:CB4239093, PMID:23524938]
-synonym: "BPBr" EXACT []
-synonym: "p-Bromophenacyl bromide" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_fluorophore XLMOD:06111 ! 4-bromophenacyl
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:06522 ! perfluorinated carboxylic acid reactive
-
-[Term]
-id: XLMOD:09035
-name: ethyl bromoacetate
-def: "Ethyl bromoacetate." [CAS:105-36-2, PubChem_Compound:7748, ChemSpiderID:7462, ChemicalBookNo:CB6852654, PMID:23524938]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:09036
-name: (2-[4-aminophenoxy]ethyl)trimethylammonium bromide
-def: "(2-[4-aminophenoxy]ethyl)trimethylammonium bromide." [ChemSpiderID:24770517, PMID:22191594]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00031 ! aldehyde reactive
-
-[Term]
-id: XLMOD:09037
-name: hydroxylammonium chloride
-def: "Hydroxylammonium chloride." [CAS:5470-11-1, PubChem_Compound:443297, ChemSpiderID:391543, ChemicalBookNo:CB8128885, PMID:22191594]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00031 ! aldehyde reactive
-
-[Term]
-id: XLMOD:09038
-name: 4-Bromobenzenesulfonyl chloride
-def: "4-Bromobenzenesulfonyl chloride." [CAS:98-58-8, ChemSpiderID:7118, ChemicalBookNo:CB8443863, PMID:22191594]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00156 ! sulfonyl chloride
-
-[Term]
-id: XLMOD:09039
-name: 7-fluoro-4-nitrobenzoxadiazole
-def: "7-fluoro-4-nitrobenzoxadiazole." [PubChem_Compound:53744831, ChemSpiderID:21375215, PMID:22191594]
-synonym: "NBD-F" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-
-[Term]
-id: XLMOD:09040
-name: diacetyl-L-tartaric anhydride
-def: "Diacetyl-L-tartaric anhydride." [CAS:6283-74-5, PubChem_Compound:102020809, ChemSpiderID:448369, ChemicalBookNo:CB0717661, PMID:22191594, PMID:26496130]
-synonym: "DATAN" EXACT []
-synonym: "DATAAN" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00166 ! anhydride
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-
-[Term]
-id: XLMOD:09041
-name: pentafluorophenacyl trifluoromethanesulfonate
-def: "Pentafluorophenacyl trifluoromethanesulfonate." [PubChem_Compound:86038332, PMID:22191594]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_fluorophore XLMOD:06110 ! phenacyl
-relationship: has_reactive_group XLMOD:00165 ! sulfonate
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-
-[Term]
-id: XLMOD:09042
-name: propyl chloroformate
-def: "Propyl chloroformate." [CAS:109-61-5, PubChem_Compound:7998, ChemSpiderID:7707, ChemicalBookNo:CB9852781, PMID:22191594]
-synonym: "PrCl" EXACT []
-is_a: XLMOD:06018 ! chloroformate reagent
-
-[Term]
-id: XLMOD:09043
-name: 12,4-dinitrofluorobenzene
-def: "12,4-dinitrofluorobenzene." [CAS:70-34-8, PubChem_Compound:6264, ChemSpiderID:21106037, ChemicalBookNo:CB9442373, PMID:22191594]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-
-[Term]
-id: XLMOD:09044
-name: trimethylsilyldiazomethane
-def: "Trimethylsilyldiazomethane." [CAS:18107-18-1, PubChem_Compound:167693, ChemSpiderID:146699, ChemicalBookNo:CB9432840, PMID:22191594, PMID:19525080]
-synonym: "TMS-DAM" EXACT []
-synonym: "TMS-DM" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-is_a: XLMOD:06013 ! TMS reagent
-relationship: is_reactive_with XLMOD:06511 ! biphosphonate drug reactive
-
-[Term]
-id: XLMOD:09045
-name: trimethyl orthoacetate
-def: "1,1,1-Trimethoxyethane." [CAS:1445-45-0, PubChem_Compound:15050, ChemSpiderID:14322, ChemicalBookNo:CB5759743, PMID:22191594]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:06511 ! biphosphonate drug reactive
-
-[Term]
-id: XLMOD:09046
-name: 3-(Perfluorooctyl)propylamine
-def: "3-(Perfluorooctyl)propylamine." [CAS:139175-50-1, PubChem_Compound:10743224, ChemSpiderID:8918555, ChemicalBookNo:CB8736444, PMID:22191594]
-synonym: "Heptadecafluoroundecylamine" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09047
-name: dimethylaminoethanol
-def: "Dimethylaminoethanol." [CAS:108-01-0, PubChem_Compound:7902, ChemSpiderID:8488535, ChemicalBookNo:CB6256870, PMID:22191594, PMID:26477276]
-synonym: "DMAE" EXACT []
-synonym: "Deanol" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09048
-name: 4-nitrobenzyl bromide
-def: "4-nitrobenzyl bromide." [CAS:100-11-8, PubChem_Compound:66011, ChemSpiderID:59402, ChemicalBookNo:CB5485712, PMID:3394930]
-synonym: "4-NBB" EXACT []
-synonym: "p-nitrobenzyl bromide" EXACT []
-is_a: XLMOD:06020 ! arylation reagent
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00168 ! benzyl bromide reactive group
-
-[Term]
-id: XLMOD:09049
-name: 2,3-pyridinedicarboxylic anhydride
-def: "2,3-pyridinedicarboxylic anhydride." [CAS:699-98-9, ChemSpiderID:62889, ChemicalBookNo:CB5268658, PMID:22191594]
-synonym: "Furo(3,4-B)Pyridine-5,7-dione" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00166 ! anhydride
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:09050
-name: ethoxyamine hydrochloride
-def: "Ethoxyamine hydrochloride." [CAS:3332-29-4, PubChem_Compound:76850, ChemSpiderID:69303, ChemicalBookNo:CB0126027, PMID:22191594]
-synonym: "Ethylhydroxylamine hydrochloride" EXACT []
-is_a: XLMOD:06002 ! alkylation reagent
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:09051
-name: 4-(N,N-Dimethylaminosulfonyl)-7-hydrazino-2,1,3-benzoxadiazole
-def: "4-(N,N-Dimethylaminosulfonyl)-7-hydrazino-2,1,3-benzoxadiazole." [CAS:131467-86-2, PubChem_Compound:131382, ChemSpiderID:116132, ChemicalBookNo:CB8688813, PMID:22191594]
-synonym: "DBD-H" EXACT []
-synonym: "4-(N,N-Dimethylsulfamoyl)-7-hydrazino-benzofurazan" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00157 ! benzofurazan
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:09052
-name: 1-(5-Fluoro-2,4-dinitrophenyl)-4-methylpiperazine
-def: "1-(5-Fluoro-2,4-dinitrophenyl)-4-methylpiperazine." [ChemSpiderID:17350721, PMID:22191594, PMID:26454158]
-synonym: "PPZ" EXACT []
-synonym: "1-(2,4-dinitro-5-fluorophenyl)-4-methylpiperazine" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_fluorophore XLMOD:06104 ! 2,4-dinitrophenyl
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:09053
-name: 4-nitrobenzoyl chloride
-def: "4-nitrobenzoyl chloride." [CAS:122-04-3, PubChem_Compound:8502, ChemSpiderID:8188, ChemicalBookNo:CB2182076, PMID:22191594]
-synonym: "4-NBC" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00155 ! acyl chloride
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:09054
-name: pyridine-3-sulfonyl chloride
-def: "Pyridine-3-sulfonyl chloride." [CAS:16133-25-8, PubChem_Compound:3164136, ChemSpiderID:2415634, ChemicalBookNo:CB5153121, PMID:26477276, PMID:22191594]
-synonym: "PSCl" EXACT []
-synonym: "chloro-3-pyridylsulfone" EXACT []
-synonym: "pyridinium-3-sulfonyl chloride" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00156 ! sulfonyl chloride
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:09055
-name: methyl acrylate
-def: "Methyl acrylate." [CAS:96-33-3, PubChem_Compound:7294, ChemSpiderID:7022, ChemicalBookNo:CB8669773, PMID:22191594]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:06513 ! thiol reactive
-
-[Term]
-id: XLMOD:09056
-name: iodoacetic acid
-def: "Iodoacetic acid." [CAS:64-69-7, PubChem_Compound:5240, ChemSpiderID:5050, ChemicalBookNo:CB3854071, PMID:22191594]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:06513 ! thiol reactive
-
-[Term]
-id: XLMOD:09057
-name: 2-Bromo-3'-methoxyacetophenone
-def: "2-Bromo-3'-methoxyacetophenone." [CAS:5000-65-7, PubChem_Compound:101294, ChemSpiderID:91526, ChemicalBookNo:CB3100727, PMID:22191594]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:06513 ! thiol reactive
-
-[Term]
-id: XLMOD:09058
-name: monobromobimane
-def: "Monobromobimane." [CAS:71418-44-5, PubChem_Compound:114810, ChemSpiderID:102775, ChemicalBookNo:CB0729365, PMID:22191594]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:06513 ! thiol reactive
-
-[Term]
-id: XLMOD:09059
-name: 4-bromo-phenacyl-bromide
-def: "4-bromo-phenacyl-bromide." [CAS:99-73-0, PubChem_Compound:7454, ChemSpiderID:7174, ChemicalBookNo:CB4239093, PMID:22191594]
-synonym: "p-BPB" EXACT []
-synonym: "p-bromo-phenacyl-bromide" EXACT []
-synonym: "2,4'-Dibromoacetophenone" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_fluorophore XLMOD:06111 ! 4-bromophenacyl
-relationship: is_reactive_with XLMOD:06513 ! thiol reactive
-
-[Term]
-id: XLMOD:09060
-name: 4-bromomethyl-7-methoxycoumarin
-def: "4-bromomethyl-7-methoxycoumarin." [CAS:35231-44-8, PubChem_Compound:121894, ChemSpiderID:108742, ChemicalBookNo:CB6345309, PMID:22191594, PMID:15897015, PMID:19525080, PMID:3394930]
-synonym: "Br-MMC" EXACT []
-synonym: "BrMMC" EXACT []
-synonym: "BMC" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_property XLMOD:00015 ! fluorescent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-relationship: is_reactive_with XLMOD:06515 ! nucleoside reactive
-
-[Term]
-id: XLMOD:09061
-name: Cookson type reagent
-def: "4-substituted 1,2,4-triazoline-3,5-dione (TAD)." [PMID:14598004]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00160 ! TAD
-
-[Term]
-id: XLMOD:09062
-name: 4-(4'-dimethylaminophenyl)-1,2,4-triazoline-3,5-dione
-def: "4-(4'-dimethylaminophenyl)-1,2,4-triazoline-3,5-dione." [PMID:24097402]
-synonym: "DAPTAD" EXACT []
-is_a: XLMOD:09061 ! Cookson type reagent
-relationship: has_reactive_group XLMOD:00160 ! TAD
-
-[Term]
-id: XLMOD:09063
-name: 4-Phenyl-1,2,4-triazole-3,5-dione
-def: "4-Phenyl-1,2,4-triazole-3,5-dione." [CAS:4233-33-4, ChemSpiderID:70304, ChemicalBookNo:CB3769656, PMID:14598004, PMID:26454158]
-synonym: "PTAD" EXACT []
-is_a: XLMOD:09061 ! Cookson type reagent
-relationship: has_reactive_group XLMOD:00160 ! TAD
-
-[Term]
-id: XLMOD:09064
-name: 4-[2-(6,7-dimethoxy-4-methyl-3-oxo-3,4-dihydroquinoxalyl)ethyl]-TAD
-def: "4-[2-(6,7-dimethoxy-4-methyl-3-oxo-3,4-dihydroquinoxalyl)ethyl]-TAD." [CAS:132788-52-4, PubChem_Compound:131554, ChemSpiderID:116261, ChemicalBookNo:CB9453782, PMID:17077543, PMID:27511712]
-synonym: "DMEQTAD" EXACT []
-is_a: XLMOD:09061 ! Cookson type reagent
-relationship: has_reactive_group XLMOD:00160 ! TAD
-
-[Term]
-id: XLMOD:09065
-name: 4-[4-(6-methoxy-2-benzoxazolyl)phenyl]-1,2,4-triazoline-3,5-dione
-def: "4-[4-(6-methoxy-2-benzoxazolyl)phenyl]-1,2,4-triazoline-3,5-dione." [PMID:15897015, PMID:27511712]
-synonym: "MBOTAD" EXACT []
-is_a: XLMOD:09061 ! Cookson type reagent
-relationship: has_reactive_group XLMOD:00160 ! TAD
-
-[Term]
-id: XLMOD:09066
-name: 4-(4-Nitrophenyl)-1,2,4-triazole-3,5-dione
-def: "4-(4-Nitrophenyl)-1,2,4-triazole-3,5-dione." [CAS:13274-75-4, PubChem_Compound:11368000, ChemSpiderID:9542917, PMID:15897015]
-synonym: "NPTAD" EXACT []
-is_a: XLMOD:09061 ! Cookson type reagent
-relationship: has_fluorophore XLMOD:06103 ! 4-nitrophenyl
-relationship: has_reactive_group XLMOD:00160 ! TAD
-
-[Term]
-id: XLMOD:09067
-name: edaravone
-def: "Edaravone." [CAS:89-25-8, PubChem_Compound:4021, ChemSpiderID:3881, ChemicalBookNo:CB1287462, PMID:20382108]
-synonym: "PMP" EXACT []
-synonym: "1-phenyl-3-methyl-5-pyrazolone" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00031 ! aldehyde reactive
-relationship: is_reactive_with XLMOD:06506 ! carbohydrate reactive
-relationship: is_reactive_with XLMOD:06510 ! ketone reactive
-
-[Term]
-id: XLMOD:09068
-name: tris(trimethoxyphenyl)phosphonium compound
-def: "Tris(trimethoxyphenyl)phosphonium compound." [PMID:11857728]
-synonym: "TMPP compound" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-
-[Term]
-id: XLMOD:09069
-name: 1S-pentafluorophenyl tris(2,4,6-trimethoxyphenyl)phosphonium acetate bromide
-def: "1S-pentafluorophenyl tris(2,4,6-trimethoxyphenyl)phosphonium acetate bromide." [PMID:12590398]
-synonym: "TMPP-AcPFP" EXACT []
-is_a: XLMOD:06009 ! chiral derivatization reagent
-is_a: XLMOD:09068 ! tris(trimethoxyphenyl)phosphonium compound
-relationship: is_reactive_with XLMOD:00031 ! aldehyde reactive
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06510 ! ketone reactive
-
-[Term]
-id: XLMOD:09070
-name: (4-hydrazino-4-oxobutyl) [tris(2,4,6-trimethoxyphenyl)phosphonium bromide
-def: "(4-hydrazino-4-oxobutyl) [tris(2,4,6-trimethoxyphenyl)phosphonium bromide." [PMID:12590398]
-synonym: "TMPP-PrG" EXACT []
-is_a: XLMOD:09068 ! tris(trimethoxyphenyl)phosphonium compound
-relationship: has_reactive_group XLMOD:00159 ! hydrazine
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-
-[Term]
-id: XLMOD:09071
-name: Tris(2,4,6,-trimethoxyphenyl)phosphonium acetic acid
-def: "Tris(2,4,6,-trimethoxyphenyl)phosphonium acetic acid." [PMID:19449318]
-synonym: "TMPP-AA" EXACT []
-synonym: "TMPP-AcCOOH" EXACT []
-is_a: XLMOD:09068 ! tris(trimethoxyphenyl)phosphonium compound
-relationship: is_reactive_with XLMOD:00031 ! aldehyde reactive
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06510 ! ketone reactive
-relationship: is_reactive_with XLMOD:06516 ! cholesterol reactive
-
-[Term]
-id: XLMOD:09072
-name: Tris(2,4,6,-trimethoxyphenyl)phosphonium ethanoic acid bromide
-def: "Tris(2,4,6,-trimethoxyphenyl)phosphonium ethanoic acid bromide." [PMID:11857728]
-synonym: "TMPP-MeCOOH" EXACT []
-is_a: XLMOD:09068 ! tris(trimethoxyphenyl)phosphonium compound
-relationship: is_reactive_with XLMOD:00031 ! aldehyde reactive
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06510 ! ketone reactive
-
-[Term]
-id: XLMOD:09073
-name: Tris(2,4,6,-trimethoxyphenyl)phosphonium propionic acid bromide
-def: "Tris(2,4,6,-trimethoxyphenyl)phosphonium propionic acid bromide." [PMID:11857728]
-synonym: "TMPP-PrCOOH" EXACT []
-is_a: XLMOD:09068 ! tris(trimethoxyphenyl)phosphonium compound
-relationship: is_reactive_with XLMOD:00031 ! aldehyde reactive
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06510 ! ketone reactive
-
-[Term]
-id: XLMOD:09074
-name: Tris(2,4,6,-trimethoxyphenyl)phosphonium propylamine bromide
-def: "Tris(2,4,6,-trimethoxyphenyl)phosphonium propylamine bromide." [PMID:11857728]
-synonym: "TMPP-PrNH2" EXACT []
-is_a: XLMOD:09068 ! tris(trimethoxyphenyl)phosphonium compound
-relationship: is_reactive_with XLMOD:00031 ! aldehyde reactive
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06510 ! ketone reactive
-
-[Term]
-id: XLMOD:09075
-name: benzoic anhydride
-def: "Benzoic anhydride." [CAS:93-97-0, PubChem_Compound:7167, ChemSpiderID:6899, ChemicalBookNo:CB1260942, PMID:15897015]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00166 ! anhydride
-
-[Term]
-id: XLMOD:09076
-name: propionic anhydride
-def: "Propionic anhydride." [CAS:123-62-6, PubChem_Compound:31263, ChemSpiderID:29003, ChemicalBookNo:CB7852974, PMID:15897015]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00166 ! anhydride
-
-[Term]
-id: XLMOD:09077
-name: 4-toluenesulfonhydrazide
-def: "4-toluenesulfonhydrazide." [CAS:1576-35-8, PubChem_Compound:15303, ChemSpiderID:14566, ChemicalBookNo:CB6156664, PMID:15897015]
-synonym: "TSH" EXACT []
-synonym: "4-Methylbenzenesulfonhydrazide" EXACT []
-synonym: "p-toluenesulfonhydrazide" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00110 ! hydrazide
-
-[Term]
-id: XLMOD:09078
-name: 2-(N,N-dimethyl-amino)ethyl acrylate
-def: "2-(N,N-dimethyl-amino)ethyl acrylate." [CAS:924-99-2, ChemSpiderID:16195, ChemicalBookNo:CB1468951, PMID:15897015]
-synonym: "DMAE acrylate" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:06513 ! thiol reactive
-
-[Term]
-id: XLMOD:09079
-name: 1-naphthylisothiocyanate
-def: "1-Naphthylisothiocyanate." [CAS:551-06-4, PubChem_Compound:11080, ChemSpiderID:10609, ChemicalBookNo:CB8696418, PMID:15897015]
-synonym: "NIT" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00162 ! isothiocyanate
-
-[Term]
-id: XLMOD:09080
-name: sulfur trioxide pyridine complex
-def: "Sulfur trioxide pyridine complex." [CAS:26412-87-3, PubChem_Compound:168533, ChemSpiderID:147422, ChemicalBookNo:CB9284694, PMID:15897015]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-
-[Term]
-id: XLMOD:09081
-name: sulfur trioxide N,N-dimethyl-formamide complex
-def: "Sulfur trioxide N,N-dimethyl-formamide complex." [CAS:29584-42-7, PubChem_Compound:169056, ChemicalBookNo:CB0234621, PMID:15897015]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-
-[Term]
-id: XLMOD:09082
-name: 2-Acrylamido-2-methyl-1-propanesulfonic acid
-def: "2-acrylamino-2-methyl-propanesulfonic acid." [CAS:15214-89-8, PubChem_Compound:65360, ChemSpiderID:58836, ChemicalBookNo:CB3470952, PMID:15897015]
-synonym: "AMDSA" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:06513 ! thiol reactive
-
-[Term]
-id: XLMOD:09083
-name: benzyl chloride
-def: "Benzyl chloride." [CAS:100-44-7, PubChem_Compound:7503, ChemSpiderID:13840690, ChemicalBookNo:CB1852583, PMID:15897015]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00155 ! acyl chloride
-
-[Term]
-id: XLMOD:09084
-name: acetic anhydride
-def: "Acetic anhydride." [CAS:108-24-7, PubChem_Compound:7918, ChemSpiderID:7630, PMID:15897015]
-synonym: "Ethanoic anhydride" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00166 ! anhydride
-
-[Term]
-id: XLMOD:09085
-name: N-methyl-4-hydrazino-7-nitrobenzofurazan
-def: "N-methyl-4-hydrazino-7-nitrobenzofurazan." [CAS:214147-22-5, PubChem_Compound:3533602, ChemSpiderID:20171264, ChemicalBookNo:CB0111892, PMID:15897015]
-synonym: "MNBDH" EXACT []
-synonym: "4-(1-Methylhydrazino)-7-nitrobenzofurazan" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00157 ! benzofurazan
-relationship: has_reactive_group XLMOD:00159 ! hydrazine
-
-[Term]
-id: XLMOD:09086
-name: boron trifluoride methanol
-def: "Boron trifluoride methanol." [CAS:373-57-9, PubChem_Compound:11062313, ChemSpiderID:9237466, ChemicalBookNo:CB1184013, PMID:15897015]
-synonym: "BF3-methanol" EXACT []
-is_a: XLMOD:06016 ! boron trifluoride reagent
-
-[Term]
-id: XLMOD:09088
-name: (3-(2-nitro-4-trifluoromethylphenyl)aminophenyl)dihydroxyborane
-def: "(3-(2-nitro-4-trifluoromethylphenyl)aminophenyl)dihydroxyborane." [PMID:15897015]
-synonym: "2NFP-APB" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-
-[Term]
-id: XLMOD:09089
-name: 2-nitro-4-trifluoromethylphenylhydrazine
-def: "2-nitro-4-trifluoromethylphenylhydrazine." [CAS:1513-50-4, PubChem_Compound:3838097, ChemSpiderID:3063768, ChemicalBookNo:CB5751590, PMID:15897015]
-synonym: "NFPH" EXACT []
-synonym: "2-NFPH" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00159 ! hydrazine
-
-[Term]
-id: XLMOD:09090
-name: 4-chloro-7-nitro-2,1,3-benzoxadiazole
-def: "4-chloro-7-nitro-2,1,3-benzoxadiazole." [CAS:10199-89-0, PubChem_Compound:25043, ChemSpiderID:23406, ChemicalBookNo:CB5173637, PMID:15897015]
-synonym: "NBDCl" EXACT []
-synonym: "4-Chloro-7-nitrobenzofurazan" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00158 ! halobenzofurazan
-
-[Term]
-id: XLMOD:09091
-name: NBD-PZ Hydrochloride
-def: "NBD-PZ Hydrochloride." [CAS:374730-75-3, PubChem_Compound:71751110, ChemSpiderID:24746629, ChemicalBookNo:CB52558061, PMID:15897015]
-synonym: "4-Nitro-7-(1-piperazinyl)-2,1,3-benzoxadiazole hydrochloride" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00158 ! halobenzofurazan
-
-[Term]
-id: XLMOD:09092
-name: sulfanilic acid
-def: "Sulfanilic acid." [CAS:121-57-3, PubChem_Compound:8479, ChemSpiderID:8166, ChemicalBookNo:CB1489237, PMID:7756703]
-synonym: "4-aminobenzenesulphonic acid" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09093
-name: 1-chloro-4-methylpyridinium iodide
-def: "1-chloro-4-methylpyridinium iodide." [ChemSpiderID:29321698, PMID:12621624]
-synonym: "CMPI" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09094
-name: 3-(2,5-dioxopyrrolidin-1-yl-oxycarbonyl)propyl]trimethylammonium chloride
-def: "3-(2,5-dioxopyrrolidin-1-yl-oxycarbonyl)propyl]trimethylammonium chloride." [PMID:22575224]
-synonym: "TMAB" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:09095
-name: N-methylnicotinic acid N-hydroxysuccinimide ester
-def: "N-methylnicotinic acid N-hydroxysuccinimide ester." [PMID:23524938, PMID:21382752]
-synonym: "C1-NA-NHS" EXACT []
-is_a: XLMOD:09005 ! NA-NHS ester
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-relationship: is_reactive_with XLMOD:06509 ! phenol reactive
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:09096
-name: deuterium labelled N-methylnicotinic acid N-hydroxysuccinimide ester
-def: "Deuterium labelled N-methylnicotinic acid N-hydroxysuccinimide ester." [PMID:23524938, PMID:23628173]
-synonym: "C1-NA-NHS-d3" EXACT []
-synonym: "C1D3-NA-NHS" EXACT []
-is_a: XLMOD:09005 ! NA-NHS ester
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-relationship: is_reactive_with XLMOD:06509 ! phenol reactive
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:09097
-name: N-propylnicotinic acid N-hydroxysuccinimide ester
-def: "N-propylnicotinic acid N-hydroxysuccinimide ester." [PMID:23524938]
-synonym: "C3-NA-NHS" EXACT []
-is_a: XLMOD:09005 ! NA-NHS ester
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-relationship: is_reactive_with XLMOD:06509 ! phenol reactive
-
-[Term]
-id: XLMOD:09098
-name: deuterium labelled N-propylnicotinic acid N-hydroxysuccinimide ester
-def: "Deuterium labelled N-propylnicotinic acid N-hydroxysuccinimide ester." [PMID:23524938]
-synonym: "C3-NA-NHS-d7" EXACT []
-synonym: "C3D7-NA-NHS" EXACT []
-is_a: XLMOD:09005 ! NA-NHS ester
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-relationship: is_reactive_with XLMOD:06509 ! phenol reactive
-
-[Term]
-id: XLMOD:09099
-name: N-butylnicotinic acid N-hydroxysuccinimide ester
-def: "N-butylnicotinic acid N-hydroxysuccinimide ester." [PMID:23524938]
-synonym: "C4-NA-NHS" EXACT []
-is_a: XLMOD:09005 ! NA-NHS ester
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-relationship: is_reactive_with XLMOD:06509 ! phenol reactive
-
-[Term]
-id: XLMOD:09100
-name: deuterium labelled N-butylnicotinic acid N-hydroxysuccinimide ester
-def: "Deuterium labelled N-butylnicotinic acid N-hydroxysuccinimide ester." [PMID:23524938]
-synonym: "C4-NA-NHS-d9" EXACT []
-synonym: "C4D9-NA-NHS" EXACT []
-is_a: XLMOD:09005 ! NA-NHS ester
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-relationship: is_reactive_with XLMOD:06509 ! phenol reactive
-
-[Term]
-id: XLMOD:09101
-name: 2,4-Dinitrofluorobenzene
-def: "2,4-Dinitrofluorobenzene." [CAS:70-34-8, PubChem_Compound:6264, ChemSpiderID:21106037, ChemicalBookNo:CB9442373, PMID:16808485]
-synonym: "DNFB" EXACT []
-synonym: "FNDB" EXACT []
-synonym: "1-Fluoro-2,4-dinitrobenzene" EXACT []
-is_a: XLMOD:09243 ! Sanger type reagent
-relationship: has_reactive_group XLMOD:00145 ! aryl halide
-
-[Term]
-id: XLMOD:09102
-name: 4-N,N,N-trimethylammonioanilylN'-hydroxysuccinimidyl carbamate iodide
-def: "4-N,N,N-trimethylammonioanilylN'-hydroxysuccinimidyl carbamate iodide." [PMID:22575224]
-synonym: "TAHS" EXACT []
-synonym: "p-N,N,N-trimethylammonioanilylN'-hydroxysuccinimidyl carbamate iodide" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00164 ! carbamate
-
-[Term]
-id: XLMOD:09103
-name: deuterium labelled p-N,N,N-trimethylammonioanilylN'-hydroxysuccinimidyl carbamate iodide
-def: "Deuterium labelled p-N,N,N-trimethylammonioanilylN'-hydroxysuccinimidyl carbamate iodide." [PMID:22575224]
-synonym: "TAHS-d3" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00164 ! carbamate
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-
-[Term]
-id: XLMOD:09104
-name: 4-methylpiperazine acetyl succinimide
-def: "4-methylpiperazine acetyl succinimide." [PMID:22575224]
-synonym: "MPAS" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-
-[Term]
-id: XLMOD:09105
-name: deuterium labelled 4-methylpiperazine acetyl succinimide
-def: "Deuterium labelled 4-methylpiperazine acetyl succinimide." [PMID:22575224]
-synonym: "MPAS-d3" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-
-[Term]
-id: XLMOD:09106
-name: 4-methylpiperadinebutyryl succinimide
-def: "4-methylpiperadinebutyryl succinimide." [PMID:22575224]
-synonym: "MPBS" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-
-[Term]
-id: XLMOD:09107
-name: deuterium labelled 4-methylpiperadinebutyryl succinimide
-def: "Deuterium labelled 4-methylpiperadinebutyryl succinimide." [PMID:22575224]
-synonym: "MPBS-d3" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-
-[Term]
-id: XLMOD:09108
-name: dimethylaminobutyryl succinimide
-def: "Dimethylaminobutyryl succinimide." [PMID:22575224]
-synonym: "DMABS" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-
-[Term]
-id: XLMOD:09109
-name: deuterium labelled dimethylaminobutyryl succinimide
-def: "Deuterium labelled dimethylaminobutyryl succinimide." [PMID:22575224]
-synonym: "DMABS-d3" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00101 ! NHS ester
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-
-[Term]
-id: XLMOD:09110
-name: 13C-dansyl chloride
-def: "13C-dansyl chloride." [PMID:22575224]
-synonym: "13C DNS-Cl" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_labelled XLMOD:00036 ! 13C labelled
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-relationship: is_reactive_with XLMOD:06509 ! phenol reactive
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-relationship: is_reactive_with XLMOD:06515 ! nucleoside reactive
-
-[Term]
-id: XLMOD:09111
-name: pentafluorophenyl-activated ester of polyethyleneglycol
-def: "Pentafluorophenyl-activated ester of polyethyleneglycol." [PMID:18954088]
-synonym: "PEG-OPFP" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00120 ! pentafluorophenyl
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-
-[Term]
-id: XLMOD:09112
-name: 13C labelled pentafluorophenyl-activated ester of polyethyleneglycol
-def: "13C labelled pentafluorophenyl-activated ester of polyethyleneglycol." [PMID:18954088]
-synonym: "13C-PEG-OPFP" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00120 ! pentafluorophenyl
-relationship: is_labelled XLMOD:00036 ! 13C labelled
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-
-[Term]
-id: XLMOD:09113
-name: cholamine
-def: "Cholamine." [ChemicalBookNo:CB8492922, PMID:22575224]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09114
-name: deuterium labelled cholamine
-def: "Deuterium labelled cholamine." [PMID:22575224]
-synonym: "cholamine-d9" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09115
-name: 2-bromo-1-methylpyridinium iodide
-def: "2-bromo-1-methylpyridinium iodide." [CAS:52693-56-8, PubChem_Compound:12233907, ChemSpiderID:11554184, ChemicalBookNo:CB13083603, PMID:22575224]
-synonym: "BMP" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09116
-name: deuterium labelled 2-bromo-1-methylpyridinium iodide
-def: "Deuterium labelled 2-bromo-1-methylpyridinium iodide." [PMID:22575224]
-synonym: "BMP-d3" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09117
-name: 3-carbinol-1-methylpyridinium iodide
-def: "3-carbinol-1-methylpyridinium iodide." [PMID:22575224]
-synonym: "CMP" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09118
-name: deuterium labelled 3-carbinol-1-methylpyridinium iodide
-def: "Deuterium labelled 3-carbinol-1-methylpyridinium iodide." [PMID:22575224]
-synonym: "CMP-d3" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09119
-name: 4-dimethylaminophenacyl bromide
-def: "4-dimethylaminophenacyl bromide." [CAS:37904-72-6, PubChem_Compound:142225, ChemSpiderID:125460, ChemicalBookNo:CB4113692, PMID:22575224]
-synonym: "DmPA-Br" EXACT []
-synonym: "2-Bromo-1-[4-(dimethylamino)phenyl]ethanone" EXACT []
-synonym: "p-dimethylaminophenacyl bromide" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_fluorophore XLMOD:06110 ! phenacyl
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09120
-name: 13C labelled p-dimethylaminophenacyl bromide
-def: "13C labelled p-dimethylaminophenacyl bromide." [PMID:22575224]
-synonym: "13C-DmPA-Br" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_fluorophore XLMOD:06110 ! phenacyl
-relationship: is_labelled XLMOD:00036 ! 13C labelled
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09121
-name: 7-(N,N-dimethylaminosulfonyl)-4-(aminoethyl)piperadino-2,1-3-benzoxadiazole
-def: "7-(N,N-dimethylaminosulfonyl)-4-(aminoethyl)piperadino-2,1-3-benzoxadiazole." [PMID:22575224]
-synonym: "DBD-PZ-NH2" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_property XLMOD:00015 ! fluorescent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09122
-name: deuterium labelled 7-(N,N-dimethylaminosulfonyl)-4-(aminoethyl)piperadino-2,1-3-benzoxadiazole
-def: "Deuterium labelled 7-(N,N-dimethylaminosulfonyl)-4-(aminoethyl)piperadino-2,1-3-benzoxadiazole." [PMID:22575224, PMID:16167303]
-synonym: "DBD-PZ-NH2-d6" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09123
-name: 7-(N,N-dimethylaminosulfonyl)-4-piperadino-2,1-3-benzoxadiazole
-def: "7-(N,N-dimethylaminosulfonyl)-4-piperadino-2,1-3-benzoxadiazole." [PMID:22575224]
-synonym: "DBD-PZ" EXACT []
-synonym: "4-(N,N-dimethylaminosulfonyl)-7-(1-piperazinyl)-2,1,3-benzoxadiazole" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_property XLMOD:00015 ! fluorescent
-relationship: has_reactive_group XLMOD:00157 ! benzofurazan
-
-[Term]
-id: XLMOD:09124
-name: deuterium labelled 7-(N,N-dimethylaminosulfonyl)-4-piperadino-2,1-3-benzoxadiazole
-def: "Deuterium labelled 7-(N,N-dimethylaminosulfonyl)-4-piperadino-2,1-3-benzoxadiazole." [PMID:22575224]
-synonym: "DBD-PZ-d6" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09125
-name: deuterium labelled Girard's reagent P
-def: "Deuterium labelled pyridinioacetohydrazide chloride." [PMID:22575224]
-synonym: "Gir P-d5" EXACT []
-synonym: "GP-d5" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: has_reactive_group XLMOD:00110 ! hydrazide
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:09126
-name: deuterium labelled 2,4-dinitrophenylhydrazine
-def: "Deuterium labelled 2,4-dinitrophenylhydrazine." [PMID:22575224]
-synonym: "DNPH-d3" EXACT []
-synonym: "2,4-Dinitro-3,5,6-trideuterophenylhydrazine" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: has_fluorophore XLMOD:06104 ! 2,4-dinitrophenyl
-relationship: has_reactive_group XLMOD:00159 ! hydrazine
-
-[Term]
-id: XLMOD:09127
-name: 2-Phenylenediamine
-def: "2-Phenylenediamine." [CAS:95-54-5, PubChem_Compound:7243, ChemSpiderID:13837582, ChemicalBookNo:CB9854699, PMID:21382752]
-synonym: "o-Phenylenediamine" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00031 ! aldehyde reactive
-relationship: is_reactive_with XLMOD:06510 ! ketone reactive
-
-[Term]
-id: XLMOD:09129
-name: 5,5'-Dithio-(bis-2-nitrobenzoic) acid
-def: "5,5'-Dithio-(bis-2-nitrobenzoic) acid." [CAS:69-78-3, PubChem_Compound:6254, ChemSpiderID:6018, ChemicalBookNo:CB2215444, PMID:21382752]
-synonym: "Ellman's reagent" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:06513 ! thiol reactive
-
-[Term]
-id: XLMOD:09130
-name: 4-(Hydroxymercuri)benzoate acid
-def: "4-(Hydroxymercuri)benzoate acid." [CAS:138-85-2, PubChem_Compound:23667696, ChemSpiderID:8104477, ChemicalBookNo:CB9350409, PMID:21382752]
-synonym: "p-(Hydroxymercuri)benzoate acid" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:06513 ! thiol reactive
-
-[Term]
-id: XLMOD:09131
-name: N-Ethylmaleimide
-def: "N-Ethylmaleimide." [CAS:128-53-0, PubChem_Compound:4362, ChemSpiderID:4209, ChemicalBookNo:CB5748314, PMID:21382752, PMID:29906677]
-synonym: "NEM" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:09132
-name: 4-Methylbenzenesulfonyl isocyanate
-def: "4-Methylbenzenesulfonyl isocyanate." [CAS:4083-64-1, PubChem_Compound:77703, ChemSpiderID:70104, ChemicalBookNo:CB8256995, PMID:21382752]
-synonym: "p-Toluenesulfonyl isocyanate" EXACT []
-synonym: "Tosyl isocyanate" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00124 ! isocyanate
-
-[Term]
-id: XLMOD:09133
-name: 1-(4-lsopropyl) phenyl-3-methyl-5-pyrazolone
-def: "1-(4-lsopropyl) phenyl-3-methyl-5-pyrazolone." [PMID:21382752]
-synonym: "PMPP" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06509 ! phenol reactive
-
-[Term]
-id: XLMOD:09134
-name: 2-Sulfobenzoic anhydride
-def: "2-Sulfobenzoic anhydride." [CAS:81-08-3, PubChem_Compound:65729, ChemSpiderID:59152, ChemicalBookNo:CB4286815, PMID:21382752]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00166 ! anhydride
-
-[Term]
-id: XLMOD:09135
-name: 1-pyrenesulfonyl chloride
-def: "1-pyrenesulfonyl chloride." [CAS:61494-52-8, PubChem_Compound:2762670, ChemSpiderID:2043373, ChemicalBookNo:CB0708281, PMID:21382752]
-synonym: "PSC" EXACT []
-synonym: "Pyrene-1-sulfonyl chloride" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00156 ! sulfonyl chloride
-
-[Term]
-id: XLMOD:09136
-name: 2,3-Naphthalenedialdehyde
-def: "2,3-Naphthalenedialdehyde." [CAS:7149-49-7, PubChem_Compound:96400, ChemSpiderID:87023, ChemicalBookNo:CB5283316, PMID:21382752]
-synonym: "Naphthalene-2,3-dicarbaldehyde" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:09137
-name: 3-chlorocarbonyl-6,7-dimethoxy-1-methyl-2(1H)-quinoxalinone
-def: "3-chlorocarbonyl-6,7-dimethoxy-1-methyl-2(1H)-quinoxalinone." [CAS:104077-15-8, PubChem_Compound:147056, ChemSpiderID:129681, ChemicalBookNo:CB6511517, PMID:21382752]
-synonym: "DMEQ-COCI" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:09138
-name: Fluorescein-5-isothiocyanate
-def: "Fluorescein-5-isothiocyanate." [CAS:3326-32-7, PubChem_Compound:18730, ChemSpiderID:17686, ChemicalBookNo:CB0173162, PMID:21382752]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_property XLMOD:00015 ! fluorescent
-relationship: has_reactive_group XLMOD:00162 ! isothiocyanate
-
-[Term]
-id: XLMOD:09139
-name: 2-Chloro-1-methylpyridinium
-def: "2-Chloro-1-methylpyridinium." [CAS:45528-84-5, PubChem_Compound:167070, ChemSpiderID:146180, ChemicalBookNo:CB11376592, PMID:21382752]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09140
-name: (5-N-succinimidoxy-5-oxopentyl)triphenylphosphonium bromide
-def: "(5-N-succinimidoxy-5-oxopentyl)triphenylphosphonium bromide." [PMID:21382752]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:09141
-name: Diethylethoxymethylenemalonate
-def: "Diethylethoxymethylenemalonate." [CAS:87-13-8, PubChem_Compound:6871, ChemSpiderID:6609, ChemicalBookNo:CB3163908, PMID:21382752, PMID:22889992]
-synonym: "DEEMM" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:09142
-name: 4-(dimethylamino)phenyl isothiocyanate
-def: "4-(dimethylamino)phenyl isothiocyanate." [CAS:2131-64-8, PubChem_Compound:75047, ChemSpiderID:67599, ChemicalBookNo:CB6742874, PMID:21382752]
-synonym: "DMAP-NCS" EXACT []
-synonym: "p-Dimethylaminophenyl isothiocyanate" EXACT []
-synonym: "p-Isothiocyanato-N,N-dimethylaniline" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00162 ! isothiocyanate
-
-[Term]
-id: XLMOD:09143
-name: 3-Nitrophenyl isothiocyanate
-def: "3-Nitrophenyl isothiocyanate." [CAS:3529-82-6, PubChem_Compound:19050, ChemSpiderID:17985, ChemicalBookNo:CB5235618, PMID:21382752]
-synonym: "m-Nitrophenyl isothiocyanate" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00162 ! isothiocyanate
-
-[Term]
-id: XLMOD:09144
-name: 3-aminopyridyl-N-hydroxysuccinimidylcarbamate
-def: "3-aminopyridyl-N-hydroxysuccinimidylcarbamate." [PMID:21382752]
-synonym: "APDS" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00164 ! carbamate
-
-[Term]
-id: XLMOD:09145
-name: N-(4-aminomethylphenyl)pyridinium
-def: "N-(4-aminomethylphenyl)pyridinium." [PMID:21382752]
-synonym: "AMPP" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09146
-name: Cyclohexanedione
-def: "Cyclohexanedione." [CAS:765-87-7, PubChem_Compound:13006, ChemSpiderID:12465, ChemicalBookNo:CB7854271, PMID:26496130]
-synonym: "CHD" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00031 ! aldehyde reactive
-relationship: is_reactive_with XLMOD:06510 ! ketone reactive
-
-[Term]
-id: XLMOD:09148
-name: 2-fluoro-1-methylpyridium
-def: "2-fluoro-1-methylpyridium." [PMID:26496130, PMID:26454158]
-synonym: "2-FMP" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00032 ! hydroxyl reactive
-relationship: is_reactive_with XLMOD:06509 ! phenol reactive
-
-[Term]
-id: XLMOD:09149
-name: triplex 5-diethylaminonaphthalene-1-sulfonyl chloride
-def: "Triplex 5-diethylaminonaphthalene-1-sulfonyl chloride." [PMID:26496130]
-synonym: "DensCl" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00156 ! sulfonyl chloride
-
-[Term]
-id: XLMOD:09150
-name: N-(5-fluoro-2,4-dinitrophenyl)-D-leucinamide
-def: "N-(5-fluoro-2,4-dinitrophenyl)-D-leucinamide." [PMID:26496130]
-synonym: "D-FDLA" EXACT []
-is_a: XLMOD:06009 ! chiral derivatization reagent
-is_a: XLMOD:09244 ! Marfey type reagent
-relationship: has_fluorophore XLMOD:06104 ! 2,4-dinitrophenyl
-
-[Term]
-id: XLMOD:09152
-name: ebselen
-def: "Ebselen." [CAS:60940-34-3, PubChem_Compound:3194, ChemSpiderID:3082, ChemicalBookNo:CB5301009, PMID:26496130]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:06513 ! thiol reactive
-
-[Term]
-id: XLMOD:09153
-name: iodoacetamide
-def: "Iodoacetamide." [CAS:144-48-9, PubChem_Compound:3727, ChemSpiderID:3596, ChemicalBookNo:CB4760867, PMID:26496130]
-synonym: "IAM" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:06513 ! thiol reactive
-
-[Term]
-id: XLMOD:09154
-name: isopropylchloroformate
-def: "Isopropylchloroformate." [CAS:108-23-6, PubChem_Compound:7917, ChemSpiderID:7629, ChemicalBookNo:CB5702693, PMID:26496130]
-synonym: "IPCF" EXACT []
-is_a: XLMOD:06018 ! chloroformate reagent
-
-[Term]
-id: XLMOD:09155
-name: 2-Nitrobenzaldehyde
-def: "2-Nitrobenzaldehyde." [CAS:552-89-6, PubChem_Compound:11101, ChemSpiderID:10630, ChemicalBookNo:CB8414184, PMID:26496130]
-synonym: "2-NB" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:06513 ! thiol reactive
-
-[Term]
-id: XLMOD:09157
-name: 5-N-succinimidoxy-5-oxopentyl)triphenylphosphonium bromide
-def: "5-N-succinimidoxy-5-oxopentyl)triphenylphosphonium bromide." [PMID:22889992]
-synonym: "SPTPP" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:09158
-name: 2,5-dioxopyrrolidin-1-yl N-tri(pyrrolidino)phosphoranylideneamino carbamate
-def: "2,5-dioxopyrrolidin-1-yl N-tri(pyrrolidino)phosphoranylideneamino carbamate." [PMID:22889992]
-synonym: "FOSF" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00164 ! carbamate
-
-[Term]
-id: XLMOD:09159
-name: 2-nitrophenylhydrazine hydrochloride
-def: "2-nitrophenylhydrazine hydrochloride." [CAS:56413-75-3, PubChem_Compound:5743520, ChemSpiderID:21306, ChemicalBookNo:CB5875432, PMID:3429573, PMID:10905720]
-synonym: "2-NPH-HCl" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00159 ! hydrazine
-
-[Term]
-id: XLMOD:09161
-name: phenacyl bromide
-def: "Phenacyl bromide." [CAS:70-11-1, PubChem_Compound:6259, ChemSpiderID:6023, ChemicalBookNo:CB6305185, PMID:3394930]
-synonym: "2-Bromoacetophenone" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_fluorophore XLMOD:06110 ! phenacyl
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09163
-name: 2-(4-nitro-benzyl)-N,N'-diisopropyl-iso-urea
-def: "2-(4-nitro-benzyl)-N,N'-diisopropyl-iso-urea." [PMID:3394930]
-synonym: "o-(4-nitro-benzyl)-N,N'-diisopropyl-iso-urea" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09164
-name: 3-nitrophenylhydrazine
-def: "3-nitrophenylhydrazine." [PMID:23580203]
-synonym: "3-NPH" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00159 ! hydrazine
-
-[Term]
-id: XLMOD:09165
-name: butyl 1-(pyridin-4-yl) piperidine 4-carboxylate
-def: "Butyl 1-(pyridin-4-yl) piperidine 4-carboxylate." [PMID:23245244]
-synonym: "BPPC" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09166
-name: 4-bromo-N-methylbenzylamine
-def: "4-bromo-N-methylbenzylamine." [CAS:699-03-6, PubChem_Compound:485400, ChemSpiderID:425634, ChemicalBookNo:CB3478655, PMID:29213145]
-synonym: "4-BNMA" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00133 ! amine reactive group
-
-[Term]
-id: XLMOD:09167
-name: N-methyl-2-phenylethanamine
-def: "N-methyl-2-phenylethanamine." [CAS:589-08-2, PubChem_Compound:11503, ChemSpiderID:11019, ChemicalBookNo:CB6140245, PMID:29213145]
-synonym: "MPEA" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09168
-name: benzoyl chloride
-def: "Benzoyl chloride." [CAS:98-88-4, PubChem_Compound:7412, ChemSpiderID:7134, ChemicalBookNo:CB8854753, PMID:28660399]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00155 ! acyl chloride
-
-[Term]
-id: XLMOD:09169
-name: N-tert-butylmaleimide
-def: "N-tert-butylmaleimide." [CAS:4144-22-3, PubChem_Compound:643190, ChemSpiderID:558357, ChemicalBookNo:CB4720254, PMID:29906677]
-synonym: "NrBM" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:09170
-name: N-propylmaleimide
-def: "N-propylmaleimide." [CAS:21746-40-7, PubChem_Compound:89033, ChemSpiderID:80338, ChemicalBookNo:CB9737837, PMID:29906677]
-synonym: "NPM" EXACT []
-synonym: "1-Propylpyrrole-2,5-dione" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:09171
-name: 4-hydrazinobenzoic acid
-def: "4-hydrazinobenzoic acid." [CAS:619-67-0, PubChem_Compound:12089, ChemSpiderID:11592, ChemicalBookNo:CB5271632, PMID:29853022]
-synonym: "HBA" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00159 ! hydrazine
-
-[Term]
-id: XLMOD:09172
-name: 2-aminoethanethiol
-def: "2-aminoethanethiol." [CAS:60-23-1, PubChem_Compound:6058, ChemSpiderID:5834, ChemicalBookNo:CB2223766, PMID:29853022]
-synonym: "Cysteamine" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00031 ! aldehyde reactive
-relationship: is_reactive_with XLMOD:06510 ! ketone reactive
-
-[Term]
-id: XLMOD:09173
-name: 2-diphenylacetyl-1,3-indandione-1-hydrazone
-def: "2-diphenylacetyl-1,3-indandione-1-hydrazone." [CAS:5102-79-4, PubChem_Compound:5375071, ChemicalBookNo:CB4455145, PMID:29853022]
-synonym: "DAIH" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-relationship: is_reactive_with XLMOD:00031 ! aldehyde reactive
-relationship: is_reactive_with XLMOD:06510 ! ketone reactive
-
-[Term]
-id: XLMOD:09174
-name: 3-methylbenzothiazolin-2-one hydrazone
-def: "3-methylbenzothiazolin-2-one hydrazone." [CAS:1128-67-2, PubChem_Compound:5359575, ChemSpiderID:4700314, ChemicalBookNo:CB2663986, PMID:29853022]
-synonym: "MBTH" EXACT []
-synonym: "(3-Methyl-1,3-benzothiazol-2-ylidene)hydrazine" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00159 ! hydrazine
-
-[Term]
-id: XLMOD:09175
-name: cyclohexane-1,3-dione
-def: "Cyclohexane-1,3-dione." [CAS:504-02-9, PubChem_Compound:10434, ChemSpiderID:10004, ChemicalBookNo:CB8319650, PMID:29853022]
-synonym: "Dihydroresorcinol" EXACT []
-synonym: "1,3-Cyclohexanedione" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00031 ! aldehyde reactive
-relationship: is_reactive_with XLMOD:06510 ! ketone reactive
-
-[Term]
-id: XLMOD:09176
-name: pyroglutamic acid succinimidyl ester
-def: "Pyroglutamic acid succinimidyl ester." [PMID:27582321]
-synonym: "PGA-OSu" EXACT []
-is_a: XLMOD:06009 ! chiral derivatization reagent
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-
-[Term]
-id: XLMOD:09177
-name: 2,4,6-trichlorophenylhydrazine
-def: "2,4,6-trichlorophenylhydrazine." [CAS:5329-12-4, PubChem_Compound:79234, ChemSpiderID:71559, ChemicalBookNo:CB4690892, PMID:29853022]
-synonym: "2,4,6-Trichlorophenylhydrazine" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00159 ! hydrazine
-
-[Term]
-id: XLMOD:09178
-name: O-2,3,4,5,6-(pentafluorobenzyl) hydroxylamine hydrochloride
-def: "O-2,3,4,5,6-(pentafluorobenzyl) hydroxylamine hydrochloride." [CAS:57981-02-9, PubChem_Compound:122307, ChemSpiderID:109062, ChemicalBookNo:CB8307815, PMID:29853022]
-synonym: "PFBO" EXACT []
-synonym: "Florox Reagent" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00031 ! aldehyde reactive
-relationship: is_reactive_with XLMOD:06510 ! ketone reactive
-
-[Term]
-id: XLMOD:09179
-name: benzoyl hydrazine
-def: "Benzoyl hydrazine." [CAS:613-94-5, PubChem_Compound:11955, ChemSpiderID:11461, ChemicalBookNo:CB2760863, PMID:29853022]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00159 ! hydrazine
-
-[Term]
-id: XLMOD:09180
-name: 2-Iodoacetanilide
-def: "2-Iodoacetanilide." [CAS:19591-17-4, PubChem_Compound:140559, ChemSpiderID:123972, ChemicalBookNo:CB2169857, PMID:29650481]
-synonym: "2-IAN" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00031 ! aldehyde reactive
-relationship: is_reactive_with XLMOD:06510 ! ketone reactive
-
-[Term]
-id: XLMOD:09181
-name: N-hydroxy-benzotriazolyl-(S)-naproxen ester
-def: "N-hydroxy-benzotriazolyl-(S)-naproxen ester." [PMID:29601646]
-synonym: "Npx-ester" EXACT []
-is_a: XLMOD:06009 ! chiral derivatization reagent
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:06517 ! histamine reactive
-
-[Term]
-id: XLMOD:09182
-name: methyl acetimidate
-def: "Methyl acetimidate." [CAS:14777-29-8, PubChem_Compound:26888, ChemSpiderID:10652948, ChemicalBookNo:CB1506534, PMID:23628173]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:09183
-name: 13C labelled methyl acetimidate
-def: "13C labelled methyl acetimidate." [PMID:23628173]
-synonym: "13C-methyl acetimidate" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_labelled XLMOD:00036 ! 13C labelled
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:09184
-name: 13C labelled formaldehyde
-def: "13C labelled formaldehyde reagent." [PMID:23628173]
-synonym: "13C-formaldehyde" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_labelled XLMOD:00036 ! 13C labelled
-relationship: has_reactive_group XLMOD:00116 ! aldehyde
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:09185
-name: acetaldehyde
-def: "Acetaldehyde." [CAS:75-07-0, PubChem_Compound:177, ChemSpiderID:172, ChemicalBookNo:CB8175809, PMID:23628173]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:09186
-name: deuterium labelled acetaldehyde
-def: "Deuterium labelled acetaldehyde." [PMID:23628173]
-synonym: "acetaldehyde-d4" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:09187
-name: 4-(4-methyl-1-piperazyl)-3-nitrobenzoyl azide
-def: "4-(4-methyl-1-piperazyl)-3-nitrobenzoyl azide." [PMID:23628173]
-synonym: "APZ" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:09188
-name: dibenzyl ethoxymethylene malonate
-def: "Dibenzyl ethoxymethylene malonate." [ChemSpiderID:48244742, PMID:26477276]
-synonym: "DBEMM" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-
-[Term]
-id: XLMOD:09189
-name: benzyl ethyl ethoxymethylene malonate
-def: "Benzyl ethyl ethoxymethylene malonate." [PMID:26477276]
-synonym: "EBEMM" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-
-[Term]
-id: XLMOD:09190
-name: diisopropyl hydrogen phosphite
-def: "Diisopropyl hydrogen phosphite." [CAS:1809-20-7, PubChem_Compound:558181, ChemSpiderID:485223, ChemicalBookNo:CB5671052, PMID:26477276]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-
-[Term]
-id: XLMOD:09191
-name: 2-(2-[7H-dibenzo (a,g)carbazol-7-yl]-ethoxy)ethyl chloroformate
-def: "2-(2-[7H-dibenzo (a,g)carbazol-7-yl]-ethoxy)ethyl chloroformate." [PMID:26477276]
-synonym: "DBCEC" EXACT []
-is_a: XLMOD:06018 ! chloroformate reagent
-
-[Term]
-id: XLMOD:09192
-name: ethyl chloroformate
-def: "Ethyl chloroformate." [CAS:541-41-3, PubChem_Compound:10928, ChemSpiderID:10465, PMID:26477276]
-synonym: "ECF" EXACT []
-is_a: XLMOD:06018 ! chloroformate reagent
-
-[Term]
-id: XLMOD:09193
-name: 1-bromobutane
-def: "1-bromobutane." [CAS:109-65-9, PubChem_Compound:8002, ChemSpiderID:7711, ChemicalBookNo:CB2852782, PMID:26477276]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09194
-name: 2-bromopyridine-5-boronic acid
-def: "2-bromopyridine-5-boronic acid." [CAS:223463-14-7, PubChem_Compound:2762706, ChemSpiderID:2043406, ChemicalBookNo:CB4371649, PMID:26477276]
-synonym: "BPBA" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00161 ! boronic acid
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:09195
-name: (3-dimethylaminophenyl)dihydroxyborane
-def: "(3-dimethylaminophenyl)dihydroxyborane." [CAS:178752-79-9, PubChem_Compound:2762527, ChemSpiderID:2043244, ChemicalBookNo:CB1220410, PMID:26477276]
-synonym: "DAPB" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:09196
-name: 1-methylimidazole-2-sulfonyl chloride
-def: "1-methylimidazole-2-sulfonyl chloride." [CAS:55694-81-0, PubChem_Compound:11658383, ChemSpiderID:9833118, ChemicalBookNo:CB22592929, PMID:26477276]
-synonym: "MLDS" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00156 ! sulfonyl chloride
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:09198
-name: N-methyl pyridinium-3-sulfonyl chloride
-def: "N-methyl pyridinium-3-sulfonyl chloride." [PMID:26477276]
-synonym: "NMPS" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00156 ! sulfonyl chloride
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:09199
-name: quaternary aminooxy reagent
-def: "Quaternary aminooxy reagent." [PMID:26477276]
-synonym: "QAO" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:09200
-name: 2,4-dimethoxy-6-piperazin-1-yl pyrimidine
-def: "2,4-dimethoxy-6-piperazin-1-yl pyrimidine." [CAS:38539-75-2, PubChem_Compound:18423149, ChemSpiderID:13408232, ChemicalBookNo:CB93096577, PMID:26477276]
-synonym: "DMPP" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09201
-name: 3-pyridylcarbinol
-def: "3-pyridylcarbinol." [CAS:100-55-0, PubChem_Compound:7510, ChemSpiderID:7229, ChemicalBookNo:CB6384809, PMID:26477276]
-synonym: "3-PC" EXACT []
-synonym: "Nicotinyl Alcohol" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09202
-name: phenylhydrazine
-def: "Phenylhydrazine." [CAS:100-63-0, PubChem_Compound:7516, ChemSpiderID:7235, ChemicalBookNo:CB9216819, PMID:26477276]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00159 ! hydrazine
-relationship: is_reactive_with XLMOD:06519 ! alpha-keto acid reactive
-
-[Term]
-id: XLMOD:09203
-name: o-benzylhydroxylamine
-def: "O-benzylhydroxylamine." [CAS:622-33-3, PubChem_Compound:102313, ChemSpiderID:92425, ChemicalBookNo:CB6853994, PMID:26477276]
-synonym: "O-BHA" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:06519 ! alpha-keto acid reactive
-
-[Term]
-id: XLMOD:09204
-name: o-phenylenediamine
-def: "O-phenylenediamine." [CAS:95-54-5, PubChem_Compound:7243, ChemSpiderID:13837582, ChemicalBookNo:CB9854699, PMID:26477276]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:06519 ! alpha-keto acid reactive
-
-[Term]
-id: XLMOD:09205
-name: benzyl alcohol
-def: "Benzyl alcohol." [CAS:100-51-6, PubChem_Compound:244, ChemSpiderID:13860335, ChemicalBookNo:CB3852587, PMID:26477276]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:06520 ! citric acid reactive
-
-[Term]
-id: XLMOD:09206
-name: 4-hydroxymercuribenzoate
-def: "4-hydroxymercuribenzoate." [PubChem_Compound:3647458, ChemSpiderID:15605527, PMID:26477276]
-synonym: "PHMB" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:06513 ! thiol reactive
-
-[Term]
-id: XLMOD:09207
-name: 4-chloro-3,5-dinitrobenzotrifluoride
-def: "4-chloro-3,5-dinitrobenzotrifluoride." [CAS:393-75-9, PubChem_Compound:9809, ChemSpiderID:9426, ChemicalBookNo:CB1329205, PMID:26477276]
-synonym: "CNBF" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:06513 ! thiol reactive
-
-[Term]
-id: XLMOD:09208
-name: omega-bromoacetonylquinolinium bromide
-def: "Omega-bromoacetonylquinolinium bromide." [PMID:26477276]
-synonym: "BQB" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:06513 ! thiol reactive
-
-[Term]
-id: XLMOD:09209
-name: pentafluorophenylhydrazine
-def: "Pentafluorophenylhydrazine." [CAS:828-73-9, PubChem_Compound:13236, ChemSpiderID:12681, ChemicalBookNo:CB4730404, PMID:26477276]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00159 ! hydrazine
-
-[Term]
-id: XLMOD:09210
-name: 7-(diethylamino)coumarin-3-carbohydrazide
-def: "7-(diethylamino)coumarin-3-carbohydrazide." [CAS:100343-98-4, PubChem_Compound:127564, ChemSpiderID:113172, ChemicalBookNo:CB0751313, PMID:26477276]
-synonym: "CHH" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00110 ! hydrazide
-
-[Term]
-id: XLMOD:09211
-name: L-Carnosine
-def: "L-Carnosine." [CAS:305-84-0, PubChem_Compound:439224, ChemSpiderID:388363, ChemicalBookNo:CB0433763, PMID:26477276]
-is_a: XLMOD:06009 ! chiral derivatization reagent
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-
-[Term]
-id: XLMOD:09212
-name: 7-fluorobenzo-2-oxa-1,3-diazole-4-sulfonate
-def: "7-fluorobenzo-2-oxa-1,3-diazole-4-sulfonate." [CAS:84806-27-9, PubChem_Compound:2737780, ChemSpiderID:108691, ChemicalBookNo:CB0175393, PMID:27582321]
-synonym: "SBD-F" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_property XLMOD:00015 ! fluorescent
-relationship: has_reactive_group XLMOD:00165 ! sulfonate
-relationship: is_reactive_with XLMOD:06513 ! thiol reactive
-
-[Term]
-id: XLMOD:09213
-name: 4-(aminosulfonyl)-7-fluoro-2,1,3-benzoxadiazole
-def: "4-(aminosulfonyl)-7-fluoro-2,1,3-benzoxadiazole." [CAS:91366-65-3, PubChem_Compound:122067, ChemSpiderID:108876, ChemicalBookNo:CB4102238, PMID:27582321]
-synonym: "ABD-F" EXACT []
-synonym: "7-Fluoro-2,1,3-benzoxadiazole-4-sulfonamide" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_property XLMOD:00015 ! fluorescent
-relationship: has_reactive_group XLMOD:00158 ! halobenzofurazan
-relationship: is_reactive_with XLMOD:06513 ! thiol reactive
-
-[Term]
-id: XLMOD:09214
-name: 4-nitro-7-(1-piperazinyl)-2,1,3-benzoxadiazole
-def: "4-nitro-7-(1-piperazinyl)-2,1,3-benzoxadiazole." [CAS:139332-66-4, PubChem_Compound:10586684, ChemSpiderID:8762060, ChemicalBookNo:CB1744464, PMID:27582321]
-synonym: "NBD-PZ" EXACT []
-synonym: "4-nitro-7-piperazino-2,1,3-benzoxadiazole" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_property XLMOD:00015 ! fluorescent
-relationship: has_reactive_group XLMOD:00157 ! benzofurazan
-
-[Term]
-id: XLMOD:09215
-name: 4-(aminosulfonyl)-7-(1-piperazinyl)-2,1,3-benzoxadiazole
-def: "4-(aminosulfonyl)-7-(1-piperazinyl)-2,1,3-benzoxadiazole." [ChemSpiderID:32684168, PMID:27582321]
-synonym: "ABD-PZ" EXACT []
-synonym: "7-(1-Piperazinyl)-2,1,3-benzoxadiazole-4-sulfonamide" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_property XLMOD:00015 ! fluorescent
-relationship: has_reactive_group XLMOD:00157 ! benzofurazan
-
-[Term]
-id: XLMOD:09216
-name: 4-(3-isothiocyanatopyrrolidin-1-yl)-7-(N,N-dimethylaminosulfonyl)-2,1,3-benzoxadiazole
-def: "4-(3-isothiocyanatopyrrolidin-1-yl)-7-(N,N-dimethylaminosulfonyl)-2,1,3-benzoxadiazole." [ChemSpiderID:3315424, PMID:27582321]
-synonym: "DBD-PyNCS" EXACT []
-synonym: "7-(3-Isothiocyanato-1-pyrrolidinyl)-N,N-dimethyl-2,1,3-benzoxadiazole-4-sulfonamide" EXACT []
-is_a: XLMOD:06009 ! chiral derivatization reagent
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_property XLMOD:00015 ! fluorescent
-relationship: has_reactive_group XLMOD:00157 ! benzofurazan
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:09217
-name: 4-(N,N-dimethylaminosulfonyl)-7-(2-carboxylpyrrolidine-1-yl)-2,1,3-benzoxadiazole
-def: "4-(N,N-dimethylaminosulfonyl)-7-(2-carboxylpyrrolidine-1-yl)-2,1,3-benzoxadiazole." [PMID:27582321]
-synonym: "DBD-Pro" EXACT []
-is_a: XLMOD:06009 ! chiral derivatization reagent
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_property XLMOD:00015 ! fluorescent
-relationship: has_reactive_group XLMOD:00157 ! benzofurazan
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:09218
-name: 4-(N,N-dimethylaminosulfonyl)-7-(2-chroloformylpyrrolidine-1-yl)-2,1,3-benzoxadiazole
-def: "4-(N,N-dimethylaminosulfonyl)-7-(2-chroloformylpyrrolidine-1-yl)-2,1,3-benzoxadiazole." [PubChem_Compound:192501, PMID:27582321]
-synonym: "DBD-ProCOCl" EXACT []
-is_a: XLMOD:06009 ! chiral derivatization reagent
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_property XLMOD:00015 ! fluorescent
-relationship: has_reactive_group XLMOD:00158 ! halobenzofurazan
-
-[Term]
-id: XLMOD:09219
-name: 4-nitro-7-(2-chroloformylpyrrolidine-1-yl)-2,1,3-benzoxadiazole
-def: "4-nitro-7-(2-chroloformylpyrrolidine-1-yl)-2,1,3-benzoxadiazole." [PMID:27582321]
-synonym: "NBD-ProCOCl" EXACT []
-is_a: XLMOD:06009 ! chiral derivatization reagent
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_property XLMOD:00015 ! fluorescent
-relationship: has_reactive_group XLMOD:00158 ! halobenzofurazan
-
-[Term]
-id: XLMOD:09220
-name: 4-(2-carbazoylpyrrolidin-1-yl)-7-(N,N-dimethylaminosulfonyl)-2,1,3-benzoxadiazole
-def: "4-(2-carbazoylpyrrolidin-1-yl)-7-(N,N-dimethylaminosulfonyl)-2,1,3-benzoxadiazole." [PMID:27582321]
-synonym: "DBD-ProCZ" EXACT []
-is_a: XLMOD:06009 ! chiral derivatization reagent
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_property XLMOD:00015 ! fluorescent
-relationship: has_reactive_group XLMOD:00157 ! benzofurazan
-
-[Term]
-id: XLMOD:09221
-name: 4-(2-carbazoylpyrrolidin-1-yl)-7-nitro-2,1,3-benzoxadiazole
-def: "4-(2-carbazoylpyrrolidin-1-yl)-7-nitro-2,1,3-benzoxadiazole." [PMID:27582321]
-synonym: "NBD-ProCZ" EXACT []
-is_a: XLMOD:06009 ! chiral derivatization reagent
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_property XLMOD:00015 ! fluorescent
-relationship: has_reactive_group XLMOD:00157 ! benzofurazan
-
-[Term]
-id: XLMOD:09222
-name: 4-(N,N-dimethylaminosulfonyl)-7-(3-aminopyrrolidin-1-yl)-2,1,3-benzoxadiazole
-def: "4-(N,N-dimethylaminosulfonyl)-7-(3-aminopyrrolidin-1-yl)-2,1,3-benzoxadiazole." [ChemSpiderID:4320363, PMID:27582321, PMID:22761132]
-synonym: "DBD-APy" EXACT []
-synonym: "7-(3-Amino-1-pyrrolidinyl)-N,N-dimethyl-2,1,3-benzoxadiazole-4-sulfonamide" EXACT []
-is_a: XLMOD:06009 ! chiral derivatization reagent
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_property XLMOD:00015 ! fluorescent
-relationship: has_reactive_group XLMOD:00157 ! benzofurazan
-
-[Term]
-id: XLMOD:09223
-name: 4-nitro-7-(3-aminopyrrolidin-1-yl)-2,1,3-benzoxadiazole
-def: "4-nitro-7-(3-aminopyrrolidin-1-yl)-2,1,3-benzoxadiazole." [ChemSpiderID:3633688, PMID:27582321]
-synonym: "NBD-APy" EXACT []
-synonym: "1-(7-Nitro-2,1,3-benzoxadiazol-4-yl)-3-pyrrolidinamine" EXACT []
-is_a: XLMOD:06009 ! chiral derivatization reagent
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_property XLMOD:00015 ! fluorescent
-relationship: has_reactive_group XLMOD:00157 ! benzofurazan
-
-[Term]
-id: XLMOD:09224
-name: 1-(3-Aminopropyl)-3-bromoquinolinium bromide
-def: "1-(3-Aminopropyl)-3-bromoquinolinium bromide." [PMID:27582321]
-synonym: "APBQ" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09225
-name: (S)-1-(4,6-Dimethoxy-1,3,5-triazin-2-yl)pyrrolidin-3-amine
-def: "(S)-1-(4,6-Dimethoxy-1,3,5-triazin-2-yl)pyrrolidin-3-amine." [PMID:27582321, PMID:26526912]
-synonym: "DMT-3(S)-Apy" EXACT []
-is_a: XLMOD:06009 ! chiral derivatization reagent
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09226
-name: (S)-2,5-dioxopyrrolidin-1-yl-1-(4,6-dimethoxy-1,3,5-triazin-2-yl) pyrrolidine-2-carboxylate
-def: "(S)-2,5-dioxopyrrolidin-1-yl-1-(4,6-dimethoxy-1,3,5-triazin-2-yl) pyrrolidine-2-carboxylate." [PMID:27582321, PMID:26526912]
-synonym: "DMT-(S)-Pro-OSu" EXACT []
-is_a: XLMOD:06009 ! chiral derivatization reagent
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00028 ! amino reactice
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-
-[Term]
-id: XLMOD:09227
-name: (R)-1-(4,6-Dimethoxy-1,3,5-triazin-2-yl)pyrrolidin-3-amine
-def: "(R)-1-(4,6-Dimethoxy-1,3,5-triazin-2-yl)pyrrolidin-3-amine." [PMID:26526912]
-synonym: "DMT-3(R)-Apy" EXACT []
-is_a: XLMOD:06009 ! chiral derivatization reagent
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09228
-name: (R)-2,5-dioxopyrrolidin-1-yl-1-(4,6-dimethoxy-1,3,5-triazin-2-yl) pyrrolidine-2-carboxylate
-def: "(R)-2,5-dioxopyrrolidin-1-yl-1-(4,6-dimethoxy-1,3,5-triazin-2-yl) pyrrolidine-2-carboxylate." [PMID:26526912]
-synonym: "DMT-(R)-Pro-OSu" EXACT []
-is_a: XLMOD:06009 ! chiral derivatization reagent
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00028 ! amino reactice
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-
-[Term]
-id: XLMOD:09229
-name: (S)-4,6-dimethoxy-N-(pyrrolidin-3-yl)-1,3,5-triazin-2-amine
-def: "(S)-4,6-dimethoxy-N-(pyrrolidin-3-yl)-1,3,5-triazin-2-amine." [PMID:25366977]
-synonym: "DMT-1(S)-Apy" EXACT []
-is_a: XLMOD:06009 ! chiral derivatization reagent
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09230
-name: (R)-4,6-dimethoxy-N-(pyrrolidin-3-yl)-1,3,5-triazin-2-amine
-def: "(R)-4,6-dimethoxy-N-(pyrrolidin-3-yl)-1,3,5-triazin-2-amine." [PMID:25366977]
-synonym: "DMT-1(R)-Apy" EXACT []
-is_a: XLMOD:06009 ! chiral derivatization reagent
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09231
-name: 4-Methyl-1,2,4-triazole-3,5-dione
-def: "4-Methyl-1,2,4-triazole-3,5-dione." [ChemSpiderID:114186, PMID:27511712]
-synonym: "MTAD" EXACT []
-synonym: "4-Methyl-TAD" EXACT []
-is_a: XLMOD:09061 ! Cookson type reagent
-relationship: has_reactive_group XLMOD:00160 ! TAD
-
-[Term]
-id: XLMOD:09232
-name: 4-(4-dimethylaminophenyl)-1,2,4-triazole-3,5-dione
-def: "4-(4-dimethylaminophenyl)-1,2,4-triazole-3,5-dione." [ChemSpiderID:28468701, PMID:27511712]
-synonym: "DMAPTAD" EXACT []
-is_a: XLMOD:09061 ! Cookson type reagent
-relationship: has_reactive_group XLMOD:00160 ! TAD
-
-[Term]
-id: XLMOD:09233
-name: deuterium labelled 4-(4-dimethylaminophenyl)-1,2,4-triazole-3,5-dione
-def: "Deuterium labelled 4-(4-dimethylaminophenyl)-1,2,4-triazole-3,5-dione." [ChemSpiderID:28468701, PMID:27511712]
-synonym: "DMAPTAD-d4" EXACT []
-is_a: XLMOD:09061 ! Cookson type reagent
-relationship: has_reactive_group XLMOD:00160 ! TAD
-
-[Term]
-id: XLMOD:09234
-name: 4-(4-diethylaminophenyl)-1,2,4-triazole-3,5-dione
-def: "4-(4-diethylaminophenyl)-1,2,4-triazole-3,5-dione." [PMID:27511712]
-synonym: "DEAPTAD" EXACT []
-is_a: XLMOD:09061 ! Cookson type reagent
-relationship: is_labelled XLMOD:00010 ! deuterium labelled
-relationship: has_reactive_group XLMOD:00160 ! TAD
-
-[Term]
-id: XLMOD:09235
-name: 2-hydrazino-4-trifluoromethylpyrimidine
-def: "2-hydrazino-4-trifluoromethylpyrimidine." [CAS:197305-97-8, ChemSpiderID:1064766, ChemicalBookNo:CB7444959, PubChem_Compound:1268079, PMID:26454158]
-synonym: "HTP" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00159 ! hydrazine
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:09236
-name: N-methyl-nicotinic acid N-hydroxysuccinimide ester
-def: "N-methyl-nicotinic acid N-hydroxysuccinimide ester." [PMID:26454158]
-synonym: "MNAHS" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00031 ! aldehyde reactive
-relationship: is_reactive_with XLMOD:06510 ! ketone reactive
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:09237
-name: o-(3-trimethylammoniumpropyl)hydroxylamine
-def: "O-(3-trimethylammoniumpropyl)hydroxylamine." [PMID:26454158]
-synonym: "TMAPH" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00031 ! aldehyde reactive
-relationship: is_reactive_with XLMOD:06510 ! ketone reactive
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:09238
-name: methoxylamine
-def: "Methoxylamine." [CAS:67-62-9, PubChem_Compound:4113, ChemSpiderID:3970, ChemicalBookNo:CB4931737, PMID:26454158]
-synonym: "OMHA" EXACT []
-synonym: "methoxyamine" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00031 ! aldehyde reactive
-relationship: has_reactive_group XLMOD:00133 ! amine reactive group
-relationship: is_reactive_with XLMOD:06510 ! ketone reactive
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:09239
-name: acetyl chloride
-def: "Acetyl chloride." [CAS:75-36-5, PubChem_Compound:6367, ChemSpiderID:6127, ChemicalBookNo:CB4485487, PMID:16458590]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00155 ! acyl chloride
-
-[Term]
-id: XLMOD:09240
-name: 2,4-dinitrobenzoyl chloride
-def: "2,4-dinitrobenzoyl chloride." [CAS:20195-22-6, PubChem_Compound:88401, ChemSpiderID:79755, ChemicalBookNo:CB6933038, PMID:17765276]
-synonym: "DNBC" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00155 ! acyl chloride
-
-[Term]
-id: XLMOD:09241
-name: 4-[2-(N,Ndimethylamino)ethylaminosulfonyl]-7-chloro-2,1,3-benzoxadiazole
-def: "4-[2-(N,Ndimethylamino)ethylaminosulfonyl]-7-chloro-2,1,3-benzoxadiazole." [CAS:664985-43-7, PubChem_Compound:44629802, ChemSpiderID:24589237, ChemicalBookNo:CB9423743, PMID:17590866]
-synonym: "DAABD-Cl" EXACT []
-synonym: "7-Chloro-N-[2-(dimethylamino)ethyl]-2,1,3-benzoxadiazole-4-sulfonamide" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00157 ! benzofurazan
-
-[Term]
-id: XLMOD:09242
-name: 4-nitrobenzenesulfonyl chloride
-def: "4-nitrobenzenesulfonyl chloride." [CAS:98-74-8, PubChem_Compound:7404, ChemSpiderID:7126, ChemicalBookNo:CB7298161, PMID:16609843]
-synonym: "4-NBSC" EXACT []
-synonym: "Nosyl chloride" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00156 ! sulfonyl chloride
-
-[Term]
-id: XLMOD:09243
-name: Sanger type reagent
-def: "A LC-MS derivatization reagent containing a fluoro-dinitrobenzene structure." [PSI:XL]
-synonym: "Sanger's reagent" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00145 ! aryl halide
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:06500 ! secondary amine reactive
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-
-[Term]
-id: XLMOD:09244
-name: Marfey type reagent
-def: "A LC-MS derivatization reagent containing a fluoro-dinitrophenyl structure." [PSI:XL]
-synonym: "Marfey's reagent" EXACT []
-synonym: "MR" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_property XLMOD:00013 ! membrane permeable
-relationship: has_reactive_group XLMOD:00145 ! aryl halide
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:06500 ! secondary amine reactive
-relationship: is_reactive_with XLMOD:06503 ! amino acid reactive
-
-[Term]
-id: XLMOD:09245
-name: N-(2,4-dinitro-5-fluorophenyl)-L-alaninamide
-def: "N-(2,4-dinitro-5-fluorophenyl)-L-alaninamide." [CAS:95713-52-3, PubChem_Compound:5486955, ChemSpiderID:4589152, ChemicalBookNo:CB5413540]
-synonym: "L-FDAA" EXACT []
-synonym: "1-Fluoro-2,4-dinitrophenyl-5-L-alanine amide" EXACT []
-is_a: XLMOD:06009 ! chiral derivatization reagent
-is_a: XLMOD:09244 ! Marfey type reagent
-relationship: has_fluorophore XLMOD:06104 ! 2,4-dinitrophenyl
-relationship: has_reactive_group XLMOD:00145 ! aryl halide
-
-[Term]
-id: XLMOD:09246
-name: N-(2,4-dinitro-5-fluorophenyl)-D-alaninamide
-def: "N-(2,4-dinitro-5-fluorophenyl)-D-alaninamide." [CAS:95713-52-3, PubChem_Compound:5486955, ChemSpiderID:4589152, ChemicalBookNo:CB5413540]
-synonym: "D-FDAA" EXACT []
-synonym: "1-Fluoro-2,4-dinitrophenyl-5-D-alanine amide" EXACT []
-is_a: XLMOD:06009 ! chiral derivatization reagent
-is_a: XLMOD:09244 ! Marfey type reagent
-relationship: has_fluorophore XLMOD:06104 ! 2,4-dinitrophenyl
-relationship: has_reactive_group XLMOD:00145 ! aryl halide
-
-[Term]
-id: XLMOD:09247
-name: N-(5-fluoro-2,4-dinitrophenyl)-L-leucinamide
-def: "N-(5-fluoro-2,4-dinitrophenyl)-L-leucinamide." [PMID:26496130]
-synonym: "L-FDLA" EXACT []
-is_a: XLMOD:06009 ! chiral derivatization reagent
-is_a: XLMOD:09244 ! Marfey type reagent
-relationship: has_fluorophore XLMOD:06104 ! 2,4-dinitrophenyl
-relationship: has_reactive_group XLMOD:00145 ! aryl halide
-
-[Term]
-id: XLMOD:09248
-name: hexyl chloroformate
-def: "Hexyl chloroformate." [CAS:6092-54-2, PubChem_Compound:22466, ChemSpiderID:21071, ChemicalBookNo:CB2782111]
-synonym: "HCF" EXACT []
-is_a: XLMOD:06018 ! chloroformate reagent
-
-[Term]
-id: XLMOD:09249
-name: 1,2-Benzo-3,4-dihydrocarbazole-9-ethyl chloroformate
-def: "1,2-Benzo-3,4-dihydrocarbazole-9-ethyl chloroformate." [PMID:18970343]
-synonym: "BCEOC" EXACT []
-is_a: XLMOD:06018 ! chloroformate reagent
-
-[Term]
-id: XLMOD:09250
-name: (-)-1-(9-fluorenyl)-ethyl chloroformate
-def: "(-)-1-(9-fluorenyl)-ethyl chloroformate." [PMID:25082527]
-synonym: "-FLEC" EXACT []
-is_a: XLMOD:06009 ! chiral derivatization reagent
-is_a: XLMOD:06018 ! chloroformate reagent
-
-[Term]
-id: XLMOD:09251
-name: (+)-1-(9-fluorenyl)-ethyl chloroformate
-def: "(+)-1-(9-fluorenyl)-ethyl chloroformate." [PMID:29785784]
-synonym: "+FLEC" EXACT []
-is_a: XLMOD:06009 ! chiral derivatization reagent
-is_a: XLMOD:06018 ! chloroformate reagent
-
-[Term]
-id: XLMOD:09252
-name: 1,2-Benzo-3,4-dihydrocarbazole-9-ethyl-benzenesulfonate
-def: "1,2-Benzo-3,4-dihydrocarbazole-9-ethyl-benzenesulfonate." [PMID:19525080, PMID:17305246]
-synonym: "BDEBS" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00165 ! sulfonate
-relationship: is_reactive_with XLMOD:06524 ! bile acid reactive
-
-[Term]
-id: XLMOD:09253
-name: 2-(2,3-Naphthalimino)ethyl trifluoromethanesulfonate
-def: "2-(2,3-Naphthalimino)ethyl trifluoromethanesulfonate." [CAS:128651-50-3, ChemSpiderID:11563131, ChemicalBookNo:CB7667550_EN, DOI:10.2116/bunsekikagaku.53.161]
-synonym: "NE-OTf" EXACT []
-synonym: "2-(2,3-Naphthalimino)ethyl trifluoromethanesulphonate" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00165 ! sulfonate
-
-[Term]
-id: XLMOD:09254
-name: 4-[2-(N,N-dimethylamino)ethylaminosulfonyl]-7-N-piperazino-2,1,3-benzoxadiazole
-def: "4-[2-(N,N-dimethylamino)ethylaminosulfonyl]-7-N-piperazino-2,1,3-benzoxadiazole." [PMID:17590866]
-synonym: "DAABD-PZ" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00157 ! benzofurazan
-
-[Term]
-id: XLMOD:09255
-name: 4-[4-carbazoylpiperidin-1-yl]-7-[2-(N,N-dimethylamino)ethylaminosulfonyl]-2,1,3-benzoxadiazole
-def: "4-[4-carbazoylpiperidin-1-yl]-7-[2-(N,N-dimethylamino)ethylaminosulfonyl]-2,1,3-benzoxadiazole." [PMID:17590866]
-synonym: "DAABD-PiCZ" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00157 ! benzofurazan
-
-[Term]
-id: XLMOD:09256
-name: 4-[2-carbazoylpyrrolidin-1-yl]-7-[2-(N,N-dimethylamino)ethylaminosulfonyl]-2,1,3-benzoxadiazole
-def: "4-[2-carbazoylpyrrolidin-1-yl]-7-[2-(N,N-dimethylamino)ethylaminosulfonyl]-2,1,3-benzoxadiazole." [PMID:17590866]
-synonym: "DAABD-ProCZ" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00157 ! benzofurazan
-
-[Term]
-id: XLMOD:09257
-name: 4-[2-(N,N-dimethylamino)ethylaminosulfonyl]-7-(3-aminopyrrolidin-1-yl)-2,1,3-benzoxadiazole
-def: "4-[2-(N,N-dimethylamino)ethylaminosulfonyl]-7-(3-aminopyrrolidin-1-yl)-2,1,3-benzoxadiazole." [PMID:17590866]
-synonym: "DAABD-APy" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00157 ! benzofurazan
-
-[Term]
-id: XLMOD:09258
-name: 4-[2-(N,N-dimethylamino)ethylaminosulfonyl]-7-N-methylhydrazino-2,1,3-benzoxadiazole
-def: "4-[2-(N,N-dimethylamino)ethylaminosulfonyl]-7-N-methylhydrazino-2,1,3-benzoxadiazole." [PMID:17703478]
-synonym: "DAABD-MHz" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00157 ! benzofurazan
-
-[Term]
-id: XLMOD:09259
-name: 4-[2-(N,N-dimethylamino) ethylaminosulfonyl]-7-(2-aminobutylamino)-2,1,3-benzoxadiazole
-def: "4-[2-(N,N-dimethylamino) ethylaminosulfonyl]-7-(2-aminobutylamino)-2,1,3-benzoxadiazole." [PMID:17703478]
-synonym: "DAABD-AB" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00157 ! benzofurazan
-
-[Term]
-id: XLMOD:09260
-name: 4-[2-(N,N-dimethylamino)ethylaminosulfonyl]-7-(2-aminopentylamino)-2,1,3-benzoxadiazole
-def: "4-[2-(N,N-dimethylamino)ethylaminosulfonyl]-7-(2-aminopentylamino)-2,1,3-benzoxadiazole." [PMID:17703478]
-synonym: "DAABD-AP" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00157 ! benzofurazan
-
-[Term]
-id: XLMOD:09261
-name: [4-(4-N-methyl)piperazinosulfonyl]-7-(2-aminoethylamino)-2,1,3-benzoxadiazole
-def: "[4-(4-N-methyl)piperazinosulfonyl]-7-(2-aminoethylamino)-2,1,3-benzoxadiazole." [PMID:17590866]
-synonym: "MePzBD-Cl" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00157 ! benzofurazan
-
-[Term]
-id: XLMOD:09262
-name: [4-(4-N-methyl)-piperazinosulfonyl]-7-chloro-2,1,3-benzoxadiazole
-def: "[4-(4-N-methyl)-piperazinosulfonyl]-7-chloro-2,1,3-benzoxadiazole." [PSI:XL]
-synonym: "MePzBD-AE" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00157 ! benzofurazan
-
-[Term]
-id: XLMOD:09263
-name: 4-[[(N-hydrazinoformyl)methyl]-N-methyl]amino-7-[N,N-(dimethylamino)sulfonyl]-2,1,3-benzoxadiazole
-def: "4-[[(N-hydrazinoformyl)methyl]-N-methyl]amino-7-[N,N-(dimethylamino)sulfonyl]-2,1,3-benzoxadiazole." [PMID:21639306]
-synonym: "DBD-COHZ" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00157 ! benzofurazan
-
-[Term]
-id: XLMOD:09264
-name: 2,4-Dinitro-6-trifluoromethylphenylhydrazine
-def: "2,4-Dinitro-6-trifluoromethylphenylhydrazine." [CAS:119-26-6, PubChem_Compound:3772977, ChemSpiderID:3001507, ChemicalBookNo:CB4852908, PMID:12502079]
-synonym: "DNFPH" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00159 ! hydrazine
-
-[Term]
-id: XLMOD:09266
-name: 2-Amino-N,N,N-trimethylethanaminium chloride
-def: "2-Amino-N,N,N-trimethylethanaminium chloride." [ChemSpiderID:2340954]
-synonym: "CA" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00133 ! amine reactive group
-
-[Term]
-id: XLMOD:09267
-name: 4-(1'-cyanoisoindolyl)phenylisothiocyanate
-def: "4-(1'-cyanoisoindolyl)phenylisothiocyanate." [PMID:12485718]
-synonym: "CIPIC" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00162 ! isothiocyanate
-
-[Term]
-id: XLMOD:09268
-name: 2,3,4,6-Tetra-O-acetyl-beta-D-glucopyranosyl isothiocyanate
-def: "2,3,4,6-Tetra-O-acetyl-beta-D-glucopyranosyl isothiocyanate." [CAS:14152-97-7, Beilstein:56699, MDL:MFCD00043085, PubChem_Compound:99462, ChemSpiderID:89858, ChemicalBookNo:CB7320022, PMID:19662356]
-synonym: "GITC" EXACT []
-synonym: "TAGIT" EXACT []
-is_a: XLMOD:06009 ! chiral derivatization reagent
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00162 ! isothiocyanate
-
-[Term]
-id: XLMOD:09269
-name: 4-Dimethylaminophenyl isothiocyanate
-def: "4-Dimethylaminophenyl isothiocyanate." [CAS:2131-64-8, PubChem_Compound:75047, ChemSpiderID:67599, ChemicalBookNo:CB6742874, PMID:23010846]
-synonym: "DMAPI" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00162 ! isothiocyanate
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:09270
-name: dimethylaminoazobenzene isothiocyanate
-def: "Dimethylaminoazobenzene isothiocyanate." [CAS:7612-98-8, PubChem_Compound:82084, ChemSpiderID:74082, ChemicalBookNo:74082, PMID:6426344]
-synonym: "DABITC" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00162 ! isothiocyanate
-
-[Term]
-id: XLMOD:09272
-name: trimellitic anhydride
-def: "Trimellitic anhydride." [CAS:552-30-7, PubChem_Compound:11089, ChemSpiderID:10618, ChemicalBookNo:CB5293056]
-synonym: "TMA" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00166 ! anhydride
-
-[Term]
-id: XLMOD:09274
-name: 3-bromoactonyltrimethylammonium bromide
-def: "3-bromoactonyltrimethylammonium bromide." [DOI:10.1016/j.trac.2014.03.013]
-synonym: "BTA" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09275
-name: 5,5'-dimethyl-1,3-cyclohexanedione
-def: "5,5'-dimethyl-1,3-cyclohexanedione." [CAS:126-81-8, PubChem_Compound:31358, ChemSpiderID:29091, ChemicalBookNo:CB1741746]
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00031 ! aldehyde reactive
-relationship: is_reactive_with XLMOD:06510 ! ketone reactive
-
-[Term]
-id: XLMOD:09276
-name: 4-(dimethylamino)-benzoic acid
-def: "4-(dimethylamino)-benzoic acid." [CAS:619-84-1, PubChem_Compound:12092, ChemSpiderID:11595, ChemicalBookNo:CB4190291]
-synonym: "DMBA" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:09277
-name: 1,2-dimethylimidazole-4-sulfonyl chloride
-def: "1,2-dimethylimidazole-4-sulfonyl chloride." [CAS:137049-02-6, PubChem_Compound:2736256, ChemSpiderID:2017929, ChemicalBookNo:CB3236772]
-synonym: "DMISC" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00156 ! sulfonyl chloride
-
-[Term]
-id: XLMOD:09278
-name: N-(2-ferroceneethyl)maleimide
-def: "N-(2-ferroceneethyl)maleimide." [ChemSpiderID:10158611]
-synonym: "FEM" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:09279
-name: ferrocenecarboxylic acid-(2-maleimidoyl)ethylamide
-def: "Ferrocenecarboxylic acid-(2-maleimidoyl)ethylamide." [DOI:10.1016/j.trac.2014.03.013]
-synonym: "FMEA" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00106 ! maleimide
-
-[Term]
-id: XLMOD:09280
-name: heptadecafluoroundecylamine
-def: "Heptadecafluoroundecylamine." [DOI:10.1016/j.trac.2014.03.013]
-synonym: "HFUA" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:06523 ! sialic acid reactive
-
-[Term]
-id: XLMOD:09281
-name: 4-hydrazino-N,N,N-trimethyl-4-oxobutanaminium iodide
-def: "4-hydrazino-N,N,N-trimethyl-4-oxobutanaminium iodide." [DOI:10.1016/j.trac.2014.03.013]
-synonym: "HTMOB" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00031 ! aldehyde reactive
-relationship: is_reactive_with XLMOD:06510 ! ketone reactive
-
-[Term]
-id: XLMOD:09282
-name: 3-aminophenylboronic acid
-def: "3-aminophenylboronic acid." [CAS:280563-63-5, PubChem_Compound:92269, ChemSpiderID:83303, ChemicalBookNo:CB3357729]
-synonym: "m-APBA" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00161 ! boronic acid
-relationship: is_reactive_with XLMOD:06512 ! steroid reactive
-
-[Term]
-id: XLMOD:09283
-name: 1,2-naphthoquinone-4-sulfonate
-def: "1,2-naphthoquinone-4-sulfonate." [CAS:2066-93-5, PubChem_Compound:10637, ChemSpiderID:10191, ChemicalBookNo:CB4898119]
-synonym: "NQS" EXACT []
-synonym: "3,4-dihydro-3,4-dioxonaphthalene-1-sulphonic acid" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00165 ! sulfonate
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:09284
-name: 2-bromo-4'-chloroacetophenone
-def: "2-bromo-4'-chloroacetophenone." [CAS:536-38-9, PubChem_Compound:68303, ChemSpiderID:61599, ChemicalBookNo:CB4198611]
-synonym: "p-CPB" EXACT []
-synonym: "4-Chloro-2'-bromoacetophenone" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00029 ! sulfhydryl reactive
-
-[Term]
-id: XLMOD:09285
-name: 1-pyrenemethylamine
-def: "1-pyrenemethylamine." [CAS:3786-54-7, PubChem_Compound:2794252, ChemSpiderID:2073158]
-synonym: "PMA" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09286
-name: succinimidylferrocenyl propionate
-def: "Succinimidylferrocenyl propionate." [PubChem_Compound:129849850]
-synonym: "SFP" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:09287
-name: N-succinimidyl-2(3-pyridyl)acetate
-def: "N-succinimidyl-2(3-pyridyl)acetate." [DOI:10.1016/j.trac.2014.03.013]
-synonym: "SPA" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-
-[Term]
-id: XLMOD:09288
-name: 7-chloro-2,1,3-benzoxadiazole-4-sulfonylaminoethyltrimethylammonium chloride
-def: "7-chloro-2,1,3-benzoxadiazole-4-sulfonylaminoethyltrimethylammonium chloride." [DOI:10.1016/j.trac.2014.03.013]
-synonym: "TAABD-Cl" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:06513 ! thiol reactive
-
-[Term]
-id: XLMOD:09289
-name: 1,2-benzo-3,4-dihydrocarbazole-9-p-toluenesulfonate
-def: "1,2-benzo-3,4-dihydrocarbazole-9-p-toluenesulfonate." [PMID:17305246]
-synonym: "BDETS" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00165 ! sulfonate
-relationship: is_reactive_with XLMOD:06524 ! bile acid reactive
-
-[Term]
-id: XLMOD:09290
-name: tetramethylammonium hydroxide
-def: "Tetramethylammonium hydroxide." [CAS:75-59-2, PubChem_Compound:60966, ChemSpiderID:54928, ChemicalBookNo:CB2854236, PMID:19525080]
-synonym: "TMAH" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-
-[Term]
-id: XLMOD:09291
-name: trimethylsulfonium hydroxide
-def: "Trimethylsulfonium hydroxide." [CAS:17287-03-5, PubChem_Compound:11105313, ChemSpiderID:9280449, ChemicalBookNo:CB1421127, PMID:19525080]
-synonym: "TMSH" EXACT []
-is_a: XLMOD:06002 ! alkylation reagent
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-
-[Term]
-id: XLMOD:09292
-name: 1-[2-(p-toluenesulfonate)-ethyl]-2-phenylimidazole-[4,5-f-]-9,10-phenantrene
-def: "1-[2-(p-toluenesulfonate)-ethyl]-2-phenylimidazole-[4,5-f-]-9,10-phenantrene." [PMID:19525080]
-synonym: "TSPP" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_property XLMOD:00015 ! fluorescent
-
-[Term]
-id: XLMOD:09293
-name: 1-pyrenyldiazomethane
-def: "1-pyrenyldiazomethane." [CAS:78377-23-8, PubChem_Compound:2762674, ChemSpiderID:2043377, ChemicalBookNo:CB1374735, DOI:10.1016/j.trac.2011.05.005]
-synonym: "PDAM" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_property XLMOD:00015 ! fluorescent
-
-[Term]
-id: XLMOD:09294
-name: 4- bromomethyl-6,7-methylenedioxycoumarin
-def: "4- bromomethyl-6,7-methylenedioxycoumarin." [CAS:97744-84-8, PubChem_Compound:126818, ChemSpiderID:112631, ChemicalBookNo:CB71326458, PMID:19525080]
-synonym: "Br-MDC" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_property XLMOD:00015 ! fluorescent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09295
-name: 9-anthryldiazomethane
-def: "9-anthryldiazomethane." [CAS:10401-59-9, PubChem_Compound:3035201, ChemSpiderID:2299498, ChemicalBookNo:CB1185515, PMID:19525080]
-synonym: "ADAM" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_property XLMOD:00015 ! fluorescent
-
-[Term]
-id: XLMOD:09296
-name: 4-bromomethyl-7,8-benzcoumarin
-def: "4-bromomethyl-7,8-benzcoumarin." [PMID:7866666]
-synonym: "BrMBC" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_property XLMOD:00015 ! fluorescent
-
-[Term]
-id: XLMOD:09297
-name: 4-diazomethyl-7-methoxycoumarin
-def: "4-diazomethyl-7-methoxycoumarin." [CAS:84471-16-9, PubChem_Compound:54478954, PMID:7866666]
-synonym: "DMMC" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_property XLMOD:00015 ! fluorescent
-
-[Term]
-id: XLMOD:09298
-name: 4-bromomethyl-7-acetoxycoumarin
-def: "4-bromomethyl-7-acetoxycoumarin." [CAS:2747-04-8, PubChem_Compound:188296, ChemSpiderID:163663, ChemicalBookNo:CB3141928, PMID:7866666]
-synonym: "BrMAC" EXACT []
-synonym: "7-Acetoxy-4-bromomethylcoumarin" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_property XLMOD:00015 ! fluorescent
-
-[Term]
-id: XLMOD:09299
-name: 4-bromomethyl-6,7-dimethoxycoumarin
-def: "4-bromomethyl-6,7-dimethoxycoumarin." [CAS:88404-25-5, PubChem_Compound:128870, ChemSpiderID:114199, ChemicalBookNo:CB8200312, PMID:7866666]
-synonym: "BrDMC" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_property XLMOD:00015 ! fluorescent
-
-[Term]
-id: XLMOD:09300
-name: N-(1-naphthyl)ethylene diamine dihydrochloride
-def: "N-(1-naphthyl)ethylene diamine dihydrochloride." [CAS:1465-25-4, PubChem_Compound:15106, ChemSpiderID:14378, ChemicalBookNo:CB4853112, PMID:19525080]
-synonym: "NEDA" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_property XLMOD:00015 ! fluorescent
-relationship: has_reactive_group XLMOD:00133 ! amine reactive group
-
-[Term]
-id: XLMOD:09301
-name: 9-aminophenanthrene
-def: "9-aminophenanthrene." [CAS:947-73-9, PubChem_Compound:13695, ChemSpiderID:13102, ChemicalBookNo:CB2175009, PMID:6707158]
-synonym: "9-AP" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_property XLMOD:00015 ! fluorescent
-relationship: has_reactive_group XLMOD:00133 ! amine reactive group
-
-[Term]
-id: XLMOD:09302
-name: 2-[p-(5,6-Methylenedioxy-2H-benzotriazol-2-yl)]phenethylamine
-def: "2-[p-(5,6-Methylenedioxy-2H-benzotriazol-2-yl)]phenethylamine." [PMID:19525080]
-synonym: "MBPA" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_property XLMOD:00015 ! fluorescent
-relationship: has_reactive_group XLMOD:00133 ! amine reactive group
-
-[Term]
-id: XLMOD:09303
-name: succinimidyloxycarbonylmethyl tris(2,4,6-trimethoxyphenyl)phosphonium bromide
-def: "Succinimidyloxycarbonylmethyl tris(2,4,6-trimethoxyphenyl)phosphonium bromide." [ChemSpiderID:24769591, PMID:20533316]
-synonym: "TMPP-Ac-OSu" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-
-[Term]
-id: XLMOD:09304
-name: 9-(hydroxymethyl)anthracene
-def: "9-(hydroxymethyl)anthracene." [CAS:1468-95-7, PubChem_Compound:73848, ChemSpiderID:66482, ChemicalBookNo:CB1205101, PMID:20533316]
-synonym: "HMA" EXACT []
-synonym: "9-Anthracenemethanol" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-
-[Term]
-id: XLMOD:09305
-name: 5-dimethylamino-1-naphthalenesulfonyl aminoethanol
-def: "5-dimethylamino-1-naphthalenesulfonyl aminoethanol." [PMID:20533316]
-synonym: "DNS-AE" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09306
-name: 2-(anthracene-2,3-dicarboximdo)ethyl-trifluoromethanesulfonate
-def: "2-(anthracene-2,3-dicarboximdo)ethyl-trifluoromethanesulfonate." [PMID:19525080]
-synonym: "AE-OTf" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00165 ! sulfonate
-
-[Term]
-id: XLMOD:09307
-name: 2-(2-naphthoxy)ethyl-2-(piperidino)ethanesulfonate
-def: "2-(2-naphthoxy)ethyl-2-(piperidino)ethanesulfonate." [ChemSpiderID:67166452, PMID:19525080]
-synonym: "NOEPES" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00165 ! sulfonate
-
-[Term]
-id: XLMOD:09308
-name: N-(4-Amidobutyl)-N-ethylisoluminol
-def: "N-(4-Amidobutyl)-N-ethylisoluminol." [CAS:66612-29-1, PubChem_Compound:196441, ChemSpiderID:170196, ChemicalBookNo:CB8393526, PMID:19525080]
-synonym: "ABEI" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-
-[Term]
-id: XLMOD:09309
-name: 6-[N-(4-aminobutyl)methylamino]-2,3-dihydro-1,4-phthalazinedione
-def: "6-[N-(4-aminobutyl)methylamino]-2,3-dihydro-1,4-phthalazinedione." [PMID:19525080]
-synonym: "ABMI" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-
-[Term]
-id: XLMOD:09310
-name: 6-[N-(3-propionohydrazino)thioureido]benzo[g]-phthalazine-1,4-(2H,3H)-dione
-def: "6-[N-(3-propionohydrazino)thioureido]benzo[g]-phthalazine-1,4-(2H,3H)-dione." [PMID:19525080]
-synonym: "PRBO" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-
-[Term]
-id: XLMOD:09311
-name: triethylamine
-def: "Triethylamine." [CAS:121-44-8, PubChem_Compound:8471, ChemSpiderID:8158, ChemicalBookNo:CB5355941]
-synonym: "TEA" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-
-[Term]
-id: XLMOD:09312
-name: trifluoroacetic acid
-def: "Trifluoroacetic acid." [CAS:76-05-1, PubChem_Compound:6422, ChemSpiderID:10239201, ChemicalBookNo:CB5127175]
-synonym: "TFA" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-
-[Term]
-id: XLMOD:09313
-name: p-Bromophenacylate
-def: "4-Bromophenacylate." [PSI:XL]
-synonym: "Phenacyl-8" EXACT []
-is_a: XLMOD:06004 ! acylation reagent
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_fluorophore XLMOD:06111 ! 4-bromophenacyl
-relationship: is_reactive_with XLMOD:00030 ! carboxyl reactive
-
-[Term]
-id: XLMOD:09314
-name: Dabsyl chloride
-def: "Dabsyl chloride." [CAS:56512-49-3, PubChem_Compound:91660, Beilstein:3064095, MDL:MFCD00007444, ChemSpiderID:82763, ChemicalBookNo:CB3699737]
-synonym: "DAB-Cl" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: has_reactive_group XLMOD:00133 ! amine reactive group
-
-[Term]
-id: XLMOD:09315
-name: 2,2-dihydroxyindane-1,3-dione
-def: "2,2-dihydroxyindane-1,3-dione." [CAS:485-47-2, PubChem_Compound:10236, ChemSpiderID:9819, ChemicalBookNo:CB1337916]
-synonym: "Ninhydrin" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
-relationship: is_reactive_with XLMOD:06500 ! secondary amine reactive
-
-[Term]
-id: XLMOD:09316
-name: 2,4,6-trinitrobenzenesulfonic acid
-def: "2,4,6-trinitrobenzenesulfonic acid." [CAS:2508-19-2, PubChem_Compound:11045, ChemSpiderID:10577, ChemicalBookNo:CB3737855]
-synonym: "TNBSA" EXACT []
-synonym: "Picrylsulfonic acid" EXACT []
-is_a: XLMOD:06010 ! LCMS derivatization reagent
-relationship: is_reactive_with XLMOD:00028 ! primary amine reactive
diff --git a/rustyms-generate-databases/data/glycosmos_glycans_list.csv.gz b/rustyms-generate-databases/data/glycosmos_glycans_list.csv.gz
deleted file mode 100644
index c77589c6..00000000
Binary files a/rustyms-generate-databases/data/glycosmos_glycans_list.csv.gz and /dev/null differ
diff --git a/rustyms-generate-databases/data/unimod.obo b/rustyms-generate-databases/data/unimod.obo
deleted file mode 100644
index 7c282fe2..00000000
--- a/rustyms-generate-databases/data/unimod.obo
+++ /dev/null
@@ -1,46331 +0,0 @@
-format-version: 1.4
-date: 12:08:2024 11:33
-
-saved-by: psi-pi_team
-default-namespace: UNIMOD
-
-[Term]
-id: UNIMOD:0
-name: unimod root node
-def: "The root node of the unimod modifications ontology." [UNIMOD:0]
-
-[Term]
-id: UNIMOD:1
-name: Acetyl
-def: "Acetylation." [RESID:AA0048, RESID:AA0049, RESID:AA0041, RESID:AA0052, RESID:AA0364, RESID:AA0056, RESID:AA0046, RESID:AA0051, RESID:AA0045, RESID:AA0354, RESID:AA0044, RESID:AA0043, PMID:11999733, URL:http\://www.ionsource.com/Card/acetylation/acetylation.htm, RESID:AA0055, PMID:14730666, PMID:15350136, RESID:AA0047, PMID:12175151, PMID:11857757, RESID:AA0042, RESID:AA0050, RESID:AA0053, RESID:AA0054, FindMod:ACET, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1]
-xref: record_id "1"
-xref: delta_mono_mass "42.010565"
-xref: delta_avge_mass "42.0367"
-xref: delta_composition "H(2) C(2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2017-11-08 16:08:56"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Multiple"
-xref: spec_1_misc_notes "PT and GIST acetyl light"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Multiple"
-xref: spec_2_misc_notes "GIST acetyl light"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "C"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "S"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Post-translational"
-xref: spec_5_group "5"
-xref: spec_5_hidden "0"
-xref: spec_5_site "N-term"
-xref: spec_5_position "Protein N-term"
-xref: spec_5_classification "Post-translational"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "T"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Post-translational"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "Y"
-xref: spec_7_position "Anywhere"
-xref: spec_7_classification "Chemical derivative"
-xref: spec_7_misc_notes "O-acetyl"
-xref: spec_8_group "8"
-xref: spec_8_hidden "1"
-xref: spec_8_site "H"
-xref: spec_8_position "Anywhere"
-xref: spec_8_classification "Chemical derivative"
-xref: spec_9_group "9"
-xref: spec_9_hidden "1"
-xref: spec_9_site "R"
-xref: spec_9_position "Anywhere"
-xref: spec_9_classification "Artefact"
-xref: spec_9_misc_notes "glyoxal-derived hydroimidazolone"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2
-name: Amidated
-def: "Amidation." [RESID:AA0088, RESID:AA0087, RESID:AA0086, RESID:AA0085, RESID:AA0084, RESID:AA0083, RESID:AA0082, RESID:AA0081, RESID:AA0089, RESID:AA0090, RESID:AA0091, RESID:AA0092, RESID:AA0093, RESID:AA0094, RESID:AA0095, RESID:AA0096, RESID:AA0097, RESID:AA0098, RESID:AA0099, RESID:AA0100, FindMod:AMID, PMID:14588022, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2]
-synonym: "Top-Down sequencing c-type fragment ion" RELATED []
-xref: record_id "2"
-xref: delta_mono_mass "-0.984016"
-xref: delta_avge_mass "-0.9848"
-xref: delta_composition "H N O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2010-06-28 10:52:25"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Protein C-term"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-xref: spec_2_misc_notes "MS/MS experiments of mass spectrometric c-ions (MS^3) can be used for protein identification by library searching. T3-sequencing is such a technique (see reference). Search engines must recognize this as a virtual modification."
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:3
-name: Biotin
-def: "Biotinylation." [RESID:AA0117, FindMod:BIOT, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=3]
-xref: record_id "3"
-xref: delta_mono_mass "226.077598"
-xref: delta_avge_mass "226.2954"
-xref: delta_composition "H(14) C(10) N(2) O(2) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2017-10-09 15:45:09"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:4
-name: Carbamidomethyl
-def: "Iodoacetamide derivative." [PMID:11510821, PMID:12422359, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=4]
-synonym: "Carboxyamidomethylation" RELATED []
-xref: record_id "4"
-xref: delta_mono_mass "57.021464"
-xref: delta_avge_mass "57.0513"
-xref: delta_composition "H(3) C(2) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2017-10-09 10:27:10"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "0"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Artefact"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "H"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Artefact"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "D"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Artefact"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "E"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Artefact"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "S"
-xref: spec_7_position "Anywhere"
-xref: spec_7_classification "Artefact"
-xref: spec_8_group "8"
-xref: spec_8_hidden "1"
-xref: spec_8_site "T"
-xref: spec_8_position "Anywhere"
-xref: spec_8_classification "Artefact"
-xref: spec_9_group "9"
-xref: spec_9_hidden "1"
-xref: spec_9_site "Y"
-xref: spec_9_position "Anywhere"
-xref: spec_9_classification "Artefact"
-xref: spec_10_group "10"
-xref: spec_10_hidden "1"
-xref: spec_10_site "U"
-xref: spec_10_position "Anywhere"
-xref: spec_10_classification "Chemical derivative"
-xref: spec_11_group "11"
-xref: spec_11_hidden "1"
-xref: spec_11_site "M"
-xref: spec_11_position "Anywhere"
-xref: spec_11_classification "Chemical derivative"
-xref: spec_11_neutral_loss_0_mono_mass "0"
-xref: spec_11_neutral_loss_0_avge_mass "0"
-xref: spec_11_neutral_loss_0_flag "false"
-xref: spec_11_neutral_loss_0_composition "0"
-xref: spec_11_neutral_loss_106_mono_mass "105.024835"
-xref: spec_11_neutral_loss_106_avge_mass "105.1588"
-xref: spec_11_neutral_loss_106_flag "false"
-xref: spec_11_neutral_loss_106_composition "H(7) C(3) N O S"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:5
-name: Carbamyl
-def: "Carbamylation." [PMID:12203680, RESID:AA0343, PMID:10978403, RESID:AA0332, URL:http\://www.ionsource.com/Card/carbam/carbam.htm, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=5]
-comment: Carbamylation is an irreversible process of non-enzymatic modification of proteins by the breakdown products of urea isocyanic acid reacts with the N-term of a proteine or side chains of lysine and arginine residues.
-xref: record_id "5"
-xref: delta_mono_mass "43.005814"
-xref: delta_avge_mass "43.0247"
-xref: delta_composition "H C N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2011-11-21 13:06:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Multiple"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Multiple"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "R"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Artefact"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "C"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Artefact"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "M"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Artefact"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "S"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "T"
-xref: spec_7_position "Anywhere"
-xref: spec_7_classification "Chemical derivative"
-xref: spec_8_group "8"
-xref: spec_8_hidden "1"
-xref: spec_8_site "Y"
-xref: spec_8_position "Anywhere"
-xref: spec_8_classification "Chemical derivative"
-xref: spec_9_group "9"
-xref: spec_9_hidden "1"
-xref: spec_9_site "N-term"
-xref: spec_9_position "Protein N-term"
-xref: spec_9_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:6
-name: Carboxymethyl
-def: "Iodoacetic acid derivative." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=6]
-synonym: "Carboxymethylation" RELATED []
-xref: record_id "6"
-xref: delta_mono_mass "58.005479"
-xref: delta_avge_mass "58.0361"
-xref: delta_composition "H(2) C(2) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2016-02-01 14:17:55"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Artefact"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "W"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_4_misc_notes "Hydroxylethanone"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "U"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:7
-name: Deamidated
-def: "Deamidation." [PMID:6838602, RESID:AA0214, URL:http\://www.ionsource.com/Card/Deamidation/deamidation.htm, FindMod:CITR, RESID:AA0128, FindMod:FLAC, PMID:15700232, FindMod:DEAM, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=7]
-synonym: "phenyllactyl from N-term Phe Citrullination" RELATED []
-xref: record_id "7"
-xref: delta_mono_mass "0.984016"
-xref: delta_avge_mass "0.9848"
-xref: delta_composition "H(-1) N(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2018-10-25 09:32:26"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_misc_notes "Convertion of glycosylated asparagine residues upon deglycosylation with PNGase F in H2O"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "R"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_2_misc_notes "Protein which is post-translationally modified by the de-imination of one or more arginine residues; Peptidylarginine deiminase (PAD) converts protein bound to citrulline"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_44_mono_mass "43.005814"
-xref: spec_2_neutral_loss_44_avge_mass "43.0247"
-xref: spec_2_neutral_loss_44_flag "false"
-xref: spec_2_neutral_loss_44_composition "H C N O"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "F"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:8
-name: ICAT-G
-def: "Gygi ICAT(TM) d0." [PMID:10504701, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=8]
-xref: record_id "8"
-xref: delta_mono_mass "486.251206"
-xref: delta_avge_mass "486.6253"
-xref: delta_composition "H(38) C(22) N(4) O(6) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-16 17:00:43"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:9
-name: ICAT-G:2H(8)
-def: "Gygi ICAT(TM) d8." [PMID:10504701, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=9]
-xref: record_id "9"
-xref: delta_mono_mass "494.30142"
-xref: delta_avge_mass "494.6746"
-xref: delta_composition "H(30) 2H(8) C(22) N(4) O(6) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-16 17:01:35"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:10
-name: Met->Hse
-def: "Homoserine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=10]
-comment: Cyanogen bromide (CNBr) cleavage converts the C-term Met to either homoserine or homoserine lactone, depending on pH.
-xref: record_id "10"
-xref: delta_mono_mass "-29.992806"
-xref: delta_avge_mass "-30.0922"
-xref: delta_composition "H(-2) C(-1) O S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-13 15:40:08"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "M"
-xref: spec_1_position "Any C-term"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:11
-name: Met->Hsl
-def: "Homoserine lactone." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=11]
-comment: Cyanogen bromide (CNBr) cleavage converts the C-term Met to either homoserine or homoserine lactone, depending on pH.
-xref: record_id "11"
-xref: delta_mono_mass "-48.003371"
-xref: delta_avge_mass "-48.1075"
-xref: delta_composition "H(-4) C(-1) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-11-14 11:10:15"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "M"
-xref: spec_1_position "Any C-term"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:12
-name: ICAT-D:2H(8)
-def: "Applied Biosystems original ICAT(TM) d8." [URL:http\://www.chemsoc.org/exemplarchem/entries/2002/proteomics/images/icat_reagent.gif, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=12]
-xref: record_id "12"
-xref: delta_mono_mass "450.275205"
-xref: delta_avge_mass "450.6221"
-xref: delta_composition "H(26) 2H(8) C(20) N(4) O(5) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-16 16:56:23"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:13
-name: ICAT-D
-def: "Applied Biosystems original ICAT(TM) d0." [URL:http\://www.chemsoc.org/exemplarchem/entries/2002/proteomics/images/icat_reagent.gif, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=13]
-xref: record_id "13"
-xref: delta_mono_mass "442.224991"
-xref: delta_avge_mass "442.5728"
-xref: delta_composition "H(34) C(20) N(4) O(5) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-16 16:53:48"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:17
-name: NIPCAM
-def: "N-isopropylcarboxamidomethyl." [PMID:8465942, PMID:11465505, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=17]
-synonym: "Dimethylacrylamide, DMA" RELATED []
-xref: record_id "17"
-xref: delta_mono_mass "99.068414"
-xref: delta_avge_mass "99.1311"
-xref: delta_composition "H(9) C(5) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-16 12:39:14"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:20
-name: PEO-Iodoacetyl-LC-Biotin
-def: "Biotinyl-iodoacetamidyl-3,6-dioxaoctanediamine." [PMID:12038753, PMID:15253424, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=20]
-synonym: "Pierce EZ-Link PEO-Iodoacetyl Biotin" RELATED []
-xref: record_id "20"
-xref: delta_mono_mass "414.193691"
-xref: delta_avge_mass "414.5196"
-xref: delta_composition "H(30) C(18) N(4) O(5) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-11-14 11:40:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:21
-name: Phospho
-def: "Phosphorylation." [RESID:AA0036, URL:http\://www.ionsource.com/Card/phos/phos.htm, RESID:AA0037, RESID:AA0033, RESID:AA0038, RESID:AA0039, RESID:AA0222, FindMod:PHOS, RESID:AA0034, RESID:AA0035, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=21]
-comment: Neutral loss of phosphate is typically observed from Y/H/D/E/K/C, rather than the preferential loss of phosphoric acid from S/T.
-xref: record_id "21"
-xref: delta_mono_mass "79.966331"
-xref: delta_avge_mass "79.9799"
-xref: delta_composition "H O(3) P"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2018-08-13 13:42:59"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_1_neutral_loss_98_mono_mass "97.976896"
-xref: spec_1_neutral_loss_98_avge_mass "97.9952"
-xref: spec_1_neutral_loss_98_flag "false"
-xref: spec_1_neutral_loss_98_composition "H(3) O(4) P"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_98_mono_mass "97.976896"
-xref: spec_1_neutral_loss_98_avge_mass "97.9952"
-xref: spec_1_neutral_loss_98_flag "false"
-xref: spec_1_neutral_loss_98_composition "H(3) O(4) P"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "Y"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "D"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-xref: spec_3_misc_notes "Rare"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "H"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Post-translational"
-xref: spec_4_misc_notes "Rare"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "C"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Post-translational"
-xref: spec_5_misc_notes "Rare"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "R"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Post-translational"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "K"
-xref: spec_7_position "Anywhere"
-xref: spec_7_classification "Post-translational"
-xref: spec_8_group "8"
-xref: spec_8_hidden "1"
-xref: spec_8_site "E"
-xref: spec_8_position "Anywhere"
-xref: spec_8_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:23
-name: Dehydrated
-def: "Dehydration." [FindMod:DHAS, RESID:AA0303, RESID:AA0302, RESID:AA0181, RESID:AA0182, FindMod:DHB, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=23]
-synonym: "didehydroalanine C-terminal imide Prompt loss of phosphate from phosphorylated residue D-Succinimide" RELATED []
-xref: record_id "23"
-xref: delta_mono_mass "-18.010565"
-xref: delta_avge_mass "-18.0153"
-xref: delta_composition "H(-2) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-11-14 11:05:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Protein C-term"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "Q"
-xref: spec_2_position "Protein C-term"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "S"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-xref: spec_3_misc_notes "beta-elimination"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "T"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Post-translational"
-xref: spec_4_misc_notes "beta-elimination"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "Y"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Post-translational"
-xref: spec_5_misc_notes "beta-elimination"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "D"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-xref: spec_7_group "7"
-xref: spec_7_hidden "0"
-xref: spec_7_site "C"
-xref: spec_7_position "Any N-term"
-xref: spec_7_classification "Artefact"
-xref: spec_7_misc_notes "Pyro-carboxymethyl as a delta from Carboxymethyl-Cys"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:24
-name: Propionamide
-def: "Acrylamide adduct." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=24]
-xref: record_id "24"
-xref: delta_mono_mass "71.037114"
-xref: delta_avge_mass "71.0779"
-xref: delta_composition "H(5) C(3) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2024-08-12 09:49:28"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:25
-name: Pyridylacetyl
-def: "Pyridylacetyl." [PMID:9276974, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=25]
-xref: record_id "25"
-xref: delta_mono_mass "119.037114"
-xref: delta_avge_mass "119.1207"
-xref: delta_composition "H(5) C(7) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-16 12:47:43"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:26
-name: Pyro-carbamidomethyl
-def: "S-carbamoylmethylcysteine cyclization (N-terminus)." [PMID:12643538, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=26]
-comment: Cyclisation of N-term Carbamidomethyl-Cys or Carboxymethyl-Cys. The delta is relative to Cys. For a delta relative to alkylated Cys, see Ammonia-loss and Dehydrated.
-synonym: "Carboxymethyl-Cys cyclization (N-terminus) Carbamidomethyl-Cys cyclization (N-terminus)" RELATED []
-xref: record_id "26"
-xref: delta_mono_mass "39.994915"
-xref: delta_avge_mass "40.0208"
-xref: delta_composition "C(2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-11-14 11:05:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "C"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:27
-name: Glu->pyro-Glu
-def: "Pyro-glu from E." [RESID:AA0031, PMID:8442665, FindMod:PYRE, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=27]
-xref: record_id "27"
-xref: delta_mono_mass "-18.010565"
-xref: delta_avge_mass "-18.0153"
-xref: delta_composition "H(-2) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2008-06-05 13:54:56"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "E"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:28
-name: Gln->pyro-Glu
-def: "Pyro-glu from Q." [RESID:AA0031, FindMod:PYRR, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=28]
-xref: record_id "28"
-xref: delta_mono_mass "-17.026549"
-xref: delta_avge_mass "-17.0305"
-xref: delta_composition "H(-3) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-13 17:06:57"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "Q"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:29
-name: SMA
-def: "N-Succinimidyl-2-morpholine acetate." [PMID:10446193, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=29]
-xref: record_id "29"
-xref: delta_mono_mass "127.063329"
-xref: delta_avge_mass "127.1412"
-xref: delta_composition "H(9) C(6) N O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2010-11-03 17:44:14"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:30
-name: Cation:Na
-def: "Sodium adduct." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=30]
-comment: Proton replaced by sodium cation.
-xref: record_id "30"
-xref: delta_mono_mass "21.981943"
-xref: delta_avge_mass "21.9818"
-xref: delta_composition "H(-1) Na"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-14 19:43:17"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Any C-term"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "D"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "E"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:31
-name: Pyridylethyl
-def: "S-pyridylethylation." [PMID:11760118, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=31]
-xref: record_id "31"
-xref: delta_mono_mass "105.057849"
-xref: delta_avge_mass "105.1372"
-xref: delta_composition "H(7) C(7) N"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-16 12:43:38"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:34
-name: Methyl
-def: "Methylation." [RESID:AA0105, PMID:11875433, RESID:AA0072, RESID:AA0299, RESID:AA0337, RESID:AA0317, RESID:AA0273, RESID:AA0234, RESID:AA0073, RESID:AA0070, RESID:AA0071, RESID:AA0076, RESID:AA0272, RESID:AA0305, RESID:AA0336, RESID:AA0069, RESID:AA0065, RESID:AA0063, RESID:AA0061, RESID:AA0064, RESID:AA0338, RESID:AA0318, FindMod:METH, URL:http\://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2921173&tool=pmcentrez&rendertype=abstract, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=34]
-synonym: "methyl ester" RELATED []
-xref: record_id "34"
-xref: delta_mono_mass "14.01565"
-xref: delta_avge_mass "14.0266"
-xref: delta_composition "H(2) C"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2015-08-26 14:39:25"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "N"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Post-translational"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "N-term"
-xref: spec_5_position "Any N-term"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "Q"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Post-translational"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "R"
-xref: spec_7_position "Anywhere"
-xref: spec_7_classification "Post-translational"
-xref: spec_8_group "8"
-xref: spec_8_hidden "1"
-xref: spec_8_site "I"
-xref: spec_8_position "Anywhere"
-xref: spec_8_classification "Post-translational"
-xref: spec_9_group "9"
-xref: spec_9_hidden "1"
-xref: spec_9_site "L"
-xref: spec_9_position "Anywhere"
-xref: spec_9_classification "Post-translational"
-xref: spec_10_group "10"
-xref: spec_10_hidden "1"
-xref: spec_10_site "N-term"
-xref: spec_10_position "Protein N-term"
-xref: spec_10_classification "Post-translational"
-xref: spec_11_group "11"
-xref: spec_11_hidden "0"
-xref: spec_11_site "C-term"
-xref: spec_11_position "Any C-term"
-xref: spec_11_classification "Multiple"
-xref: spec_12_group "12"
-xref: spec_12_hidden "0"
-xref: spec_12_site "E"
-xref: spec_12_position "Anywhere"
-xref: spec_12_classification "Post-translational"
-xref: spec_12_group "12"
-xref: spec_12_hidden "0"
-xref: spec_12_site "D"
-xref: spec_12_position "Anywhere"
-xref: spec_12_classification "Post-translational"
-xref: spec_13_group "13"
-xref: spec_13_hidden "1"
-xref: spec_13_site "S"
-xref: spec_13_position "Anywhere"
-xref: spec_13_classification "Post-translational"
-xref: spec_14_group "14"
-xref: spec_14_hidden "1"
-xref: spec_14_site "T"
-xref: spec_14_position "Anywhere"
-xref: spec_14_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:35
-name: Oxidation
-def: "Oxidation or Hydroxylation." [RESID:AA0027, PMID:11461766, RESID:AA0029, RESID:AA0028, RESID:AA0030, PMID:9004526, RESID:AA0205, RESID:AA0146, FindMod:DOPA, RESID:AA0215, FindMod:CSEA, RESID:AA0026, PMID:14661084, PMID:15569593, PMID:11120890, PMID:11212008, RESID:AA0322, RESID:AA0235, FindMod:HYDR, PMID:14661085, PMID:12781462, PMID:2057999, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=35]
-xref: record_id "35"
-xref: delta_mono_mass "15.994915"
-xref: delta_avge_mass "15.9994"
-xref: delta_composition "O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2017-10-06 17:05:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_1_misc_notes "3-hydroxyaspartic acid"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-xref: spec_3_misc_notes "3-hydroxyasparagine"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "P"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Post-translational"
-xref: spec_4_misc_notes "glutamic semialdehyde"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "F"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Artefact"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "Y"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Post-translational"
-xref: spec_6_misc_notes "dihydroxyphenylalanine (DOPA)"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "R"
-xref: spec_7_position "Anywhere"
-xref: spec_7_classification "Post-translational"
-xref: spec_8_group "8"
-xref: spec_8_hidden "0"
-xref: spec_8_site "M"
-xref: spec_8_position "Anywhere"
-xref: spec_8_classification "Artefact"
-xref: spec_8_misc_notes "methionine sulfoxide"
-xref: spec_8_neutral_loss_0_mono_mass "0"
-xref: spec_8_neutral_loss_0_avge_mass "0"
-xref: spec_8_neutral_loss_0_flag "false"
-xref: spec_8_neutral_loss_0_composition "0"
-xref: spec_8_neutral_loss_64_mono_mass "63.998285"
-xref: spec_8_neutral_loss_64_avge_mass "64.1069"
-xref: spec_8_neutral_loss_64_flag "false"
-xref: spec_8_neutral_loss_64_composition "H(4) C O S"
-xref: spec_9_group "9"
-xref: spec_9_hidden "1"
-xref: spec_9_site "C"
-xref: spec_9_position "Anywhere"
-xref: spec_9_classification "Post-translational"
-xref: spec_9_misc_notes "sulfenic acid"
-xref: spec_10_group "10"
-xref: spec_10_hidden "0"
-xref: spec_10_site "W"
-xref: spec_10_position "Anywhere"
-xref: spec_10_classification "Artefact"
-xref: spec_10_group "10"
-xref: spec_10_hidden "0"
-xref: spec_10_site "H"
-xref: spec_10_position "Anywhere"
-xref: spec_10_classification "Artefact"
-xref: spec_10_misc_notes "2-oxohistidine"
-xref: spec_11_group "11"
-xref: spec_11_hidden "1"
-xref: spec_11_site "G"
-xref: spec_11_position "Any C-term"
-xref: spec_11_classification "Pre-translational"
-xref: spec_11_misc_notes "Hydroxyglycine derivative in amidation pathway"
-xref: spec_12_group "12"
-xref: spec_12_hidden "1"
-xref: spec_12_site "U"
-xref: spec_12_position "Anywhere"
-xref: spec_12_classification "Multiple"
-xref: spec_13_group "13"
-xref: spec_13_hidden "1"
-xref: spec_13_site "E"
-xref: spec_13_position "Anywhere"
-xref: spec_13_classification "Chemical derivative"
-xref: spec_13_misc_notes "hydroxyglutamic acid"
-xref: spec_14_group "14"
-xref: spec_14_hidden "1"
-xref: spec_14_site "I"
-xref: spec_14_position "Anywhere"
-xref: spec_14_classification "Chemical derivative"
-xref: spec_15_group "15"
-xref: spec_15_hidden "1"
-xref: spec_15_site "L"
-xref: spec_15_position "Anywhere"
-xref: spec_15_classification "Chemical derivative"
-xref: spec_16_group "16"
-xref: spec_16_hidden "1"
-xref: spec_16_site "Q"
-xref: spec_16_position "Anywhere"
-xref: spec_16_classification "Chemical derivative"
-xref: spec_17_group "17"
-xref: spec_17_hidden "1"
-xref: spec_17_site "S"
-xref: spec_17_position "Anywhere"
-xref: spec_17_classification "Chemical derivative"
-xref: spec_18_group "18"
-xref: spec_18_hidden "1"
-xref: spec_18_site "T"
-xref: spec_18_position "Anywhere"
-xref: spec_18_classification "Chemical derivative"
-xref: spec_19_group "19"
-xref: spec_19_hidden "1"
-xref: spec_19_site "V"
-xref: spec_19_position "Anywhere"
-xref: spec_19_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:36
-name: Dimethyl
-def: "Di-Methylation." [FindMod:DIMETH, RESID:AA0311, RESID:AA0068, PMID:14570711, RESID:AA0067, PMID:12964758, RESID:AA0075, RESID:AA0066, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=36]
-xref: record_id "36"
-xref: delta_mono_mass "28.0313"
-xref: delta_avge_mass "28.0532"
-xref: delta_composition "H(4) C(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2014-11-16 07:37:54"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Multiple"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "R"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Isotopic label"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "N"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Post-translational"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "P"
-xref: spec_5_position "Protein N-term"
-xref: spec_5_classification "Post-translational"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "N-term"
-xref: spec_6_position "Protein N-term"
-xref: spec_6_classification "Isotopic label"
-xref: spec_6_misc_notes "When dimethyl labelling is pre-digest"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:37
-name: Trimethyl
-def: "Tri-Methylation." [FindMod:TRIMETH, RESID:AA0062, RESID:AA0074, PMID:12590383, URL:http\://pir.georgetown.edu/resid/faq.shtml#q12, URL:http\://www.cancerci.com/content/1/1/3, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=37]
-xref: record_id "37"
-xref: delta_mono_mass "42.04695"
-xref: delta_avge_mass "42.0797"
-xref: delta_composition "H(6) C(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2015-05-22 13:05:59"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_60_mono_mass "59.073499"
-xref: spec_1_neutral_loss_60_avge_mass "59.1103"
-xref: spec_1_neutral_loss_60_flag "false"
-xref: spec_1_neutral_loss_60_composition "H(9) C(3) N"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "R"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "A"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:39
-name: Methylthio
-def: "Beta-methylthiolation." [RESID:AA0320, PMID:8844851, URL:http\://www.trc-canada.com/white_papers.lasso, RESID:AA0232, URL:http\://docs.appliedbiosystems.com/pebiodocs/04351918.pdf, RESID:AA0101, FindMod:BMTH, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=39]
-synonym: "Methyl methanethiosulfonate MMTS" RELATED []
-xref: record_id "39"
-xref: delta_mono_mass "45.987721"
-xref: delta_avge_mass "46.0916"
-xref: delta_composition "H(2) C S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2011-11-24 16:48:21"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "0"
-xref: spec_3_site "C"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Multiple"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "N-term"
-xref: spec_4_position "Any N-term"
-xref: spec_4_classification "Artefact"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "K"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:40
-name: Sulfo
-def: "O-Sulfonation." [RESID:AA0172, PMID:14752058, RESID:AA0362, FindMod:SULF, RESID:AA0171, RESID:AA0361, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=40]
-xref: record_id "40"
-xref: delta_mono_mass "79.956815"
-xref: delta_avge_mass "80.0632"
-xref: delta_composition "O(3) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2012-02-14 17:50:32"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_1_misc_notes "Because the modification is quantitatively lost on CID, site assigment is not possible when there is a choice of sites"
-xref: spec_1_neutral_loss_80_mono_mass "79.956815"
-xref: spec_1_neutral_loss_80_avge_mass "80.0632"
-xref: spec_1_neutral_loss_80_flag "false"
-xref: spec_1_neutral_loss_80_composition "O(3) S"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_1_misc_notes "Because the modification is quantitatively lost on CID, site assigment is not possible when there is a choice of sites"
-xref: spec_1_neutral_loss_80_mono_mass "79.956815"
-xref: spec_1_neutral_loss_80_avge_mass "80.0632"
-xref: spec_1_neutral_loss_80_flag "false"
-xref: spec_1_neutral_loss_80_composition "O(3) S"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_1_misc_notes "Because the modification is quantitatively lost on CID, site assigment is not possible when there is a choice of sites"
-xref: spec_1_neutral_loss_80_mono_mass "79.956815"
-xref: spec_1_neutral_loss_80_avge_mass "80.0632"
-xref: spec_1_neutral_loss_80_flag "false"
-xref: spec_1_neutral_loss_80_composition "O(3) S"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_2_misc_notes "Sulfitolysis"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:41
-name: Hex
-def: "Hexose." [RESID:AA0217, RESID:AA0152, PMID:15279557, FindMod:GLUC, URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&mode=exact, RESID:AA0157, FindMod:CMAN, RESID:AA0327, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=41]
-synonym: "Fructose Mannose Galactose Glucose" RELATED []
-xref: record_id "41"
-xref: delta_mono_mass "162.052824"
-xref: delta_avge_mass "162.1406"
-xref: delta_composition "Hex"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2018-06-27 13:23:10"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other glycosylation"
-xref: spec_1_misc_notes "glycation"
-xref: spec_1_neutral_loss_55_mono_mass "54.031694"
-xref: spec_1_neutral_loss_55_avge_mass "54.0458"
-xref: spec_1_neutral_loss_55_flag "false"
-xref: spec_1_neutral_loss_55_composition "H(6) O(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other glycosylation"
-xref: spec_1_misc_notes "glycation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_55_mono_mass "54.031694"
-xref: spec_1_neutral_loss_55_avge_mass "54.0458"
-xref: spec_1_neutral_loss_55_flag "false"
-xref: spec_1_neutral_loss_55_composition "H(6) O(3)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_163_mono_mass "162.052824"
-xref: spec_2_neutral_loss_163_avge_mass "162.1406"
-xref: spec_2_neutral_loss_163_flag "false"
-xref: spec_2_neutral_loss_163_composition "Hex"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Other glycosylation"
-xref: spec_3_misc_notes "glycation"
-xref: spec_3_neutral_loss_0_mono_mass "0"
-xref: spec_3_neutral_loss_0_avge_mass "0"
-xref: spec_3_neutral_loss_0_flag "false"
-xref: spec_3_neutral_loss_0_composition "0"
-xref: spec_3_neutral_loss_55_mono_mass "54.031694"
-xref: spec_3_neutral_loss_55_avge_mass "54.0458"
-xref: spec_3_neutral_loss_55_flag "false"
-xref: spec_3_neutral_loss_55_composition "H(6) O(3)"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "T"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "O-linked glycosylation"
-xref: spec_4_neutral_loss_163_mono_mass "162.052824"
-xref: spec_4_neutral_loss_163_avge_mass "162.1406"
-xref: spec_4_neutral_loss_163_flag "false"
-xref: spec_4_neutral_loss_163_composition "Hex"
-xref: spec_4_neutral_loss_0_mono_mass "0"
-xref: spec_4_neutral_loss_0_avge_mass "0"
-xref: spec_4_neutral_loss_0_flag "false"
-xref: spec_4_neutral_loss_0_composition "0"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "S"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "O-linked glycosylation"
-xref: spec_4_neutral_loss_163_mono_mass "162.052824"
-xref: spec_4_neutral_loss_163_avge_mass "162.1406"
-xref: spec_4_neutral_loss_163_flag "false"
-xref: spec_4_neutral_loss_163_composition "Hex"
-xref: spec_4_neutral_loss_0_mono_mass "0"
-xref: spec_4_neutral_loss_0_avge_mass "0"
-xref: spec_4_neutral_loss_0_flag "false"
-xref: spec_4_neutral_loss_0_composition "0"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "W"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Other glycosylation"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "C"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Other glycosylation"
-xref: spec_8_group "8"
-xref: spec_8_hidden "1"
-xref: spec_8_site "Y"
-xref: spec_8_position "Anywhere"
-xref: spec_8_classification "O-linked glycosylation"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:42
-name: Lipoyl
-def: "Lipoyl." [RESID:AA0118, FindMod:LIPY, PMID:3522581, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=42]
-comment: This group is normally a substituent on N6 of a lysine residue of an enzyme or other protein.
-xref: record_id "42"
-xref: delta_mono_mass "188.032956"
-xref: delta_avge_mass "188.3103"
-xref: delta_composition "H(12) C(8) O S(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-16 15:06:53"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:43
-name: HexNAc
-def: "N-Acetylhexosamine." [FindMod:GLCN, RESID:AA0155, PMID:3086323, RESID:AA0154, RESID:AA0151, URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=43]
-comment: The amine derivative of a hexose formed by replacing a hydroxyl group with an amino group.(+acetyl group).
-xref: record_id "43"
-xref: delta_mono_mass "203.079373"
-xref: delta_avge_mass "203.1925"
-xref: delta_composition "HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2024-08-12 09:50:41"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_204_mono_mass "203.079373"
-xref: spec_1_neutral_loss_204_avge_mass "203.1925"
-xref: spec_1_neutral_loss_204_flag "false"
-xref: spec_1_neutral_loss_204_composition "HexNAc"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_204_mono_mass "203.079373"
-xref: spec_2_neutral_loss_204_avge_mass "203.1925"
-xref: spec_2_neutral_loss_204_flag "false"
-xref: spec_2_neutral_loss_204_composition "HexNAc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_204_mono_mass "203.079373"
-xref: spec_2_neutral_loss_204_avge_mass "203.1925"
-xref: spec_2_neutral_loss_204_flag "false"
-xref: spec_2_neutral_loss_204_composition "HexNAc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "C"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Other glycosylation"
-xref: spec_3_neutral_loss_204_mono_mass "203.079373"
-xref: spec_3_neutral_loss_204_avge_mass "203.1925"
-xref: spec_3_neutral_loss_204_flag "false"
-xref: spec_3_neutral_loss_204_composition "HexNAc"
-xref: spec_3_neutral_loss_0_mono_mass "0"
-xref: spec_3_neutral_loss_0_avge_mass "0"
-xref: spec_3_neutral_loss_0_flag "false"
-xref: spec_3_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:44
-name: Farnesyl
-def: "Farnesylation." [PMID:15609361, RESID:AA0102, FindMod:FARN, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=44]
-xref: record_id "44"
-xref: delta_mono_mass "204.187801"
-xref: delta_avge_mass "204.3511"
-xref: delta_composition "H(24) C(15)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-16 15:11:38"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:45
-name: Myristoyl
-def: "Myristoylation." [RESID:AA0059, RESID:AA0307, RESID:AA0078, FindMod:MYRI, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=45]
-xref: record_id "45"
-xref: delta_mono_mass "210.198366"
-xref: delta_avge_mass "210.3556"
-xref: delta_composition "H(26) C(14) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-16 15:13:17"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "C"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:46
-name: PyridoxalPhosphate
-def: "Pyridoxal phosphate." [RESID:AA0119, FindMod:PLP, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=46]
-comment: The co-enzyme derivative of vitamin B6. Forms Schiff\'s bases of substrate amino acids during catalysis of transamination, decarboxylation and racemisation reactions.
-xref: record_id "46"
-xref: delta_mono_mass "229.014009"
-xref: delta_avge_mass "229.1266"
-xref: delta_composition "H(8) C(8) N O(5) P"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-16 15:35:42"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:47
-name: Palmitoyl
-def: "Palmitoylation." [RESID:AA0080, RESID:AA0079, RESID:AA0106, RESID:AA0077, FindMod:PALM, RESID:AA0339, RESID:AA0060, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=47]
-comment: Palmitoylation is a post-translational modification that consists in the addition of a 16 carbons fatty acid, palmitate, to a cysteine residue through the creation of a thioester link.
-xref: record_id "47"
-xref: delta_mono_mass "238.229666"
-xref: delta_avge_mass "238.4088"
-xref: delta_composition "H(30) C(16) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-16 15:38:43"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "S"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "T"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Post-translational"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "N-term"
-xref: spec_5_position "Protein N-term"
-xref: spec_5_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:48
-name: GeranylGeranyl
-def: "Geranyl-geranyl." [RESID:AA0104, PMID:15609361, FindMod:GERA, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=48]
-xref: record_id "48"
-xref: delta_mono_mass "272.250401"
-xref: delta_avge_mass "272.4681"
-xref: delta_composition "H(32) C(20)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-16 15:47:48"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:49
-name: Phosphopantetheine
-def: "Phosphopantetheine." [RESID:AA0150, FindMod:PPAN, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=49]
-comment: Protein which contains at least one phosphopantetheine as the prosthetic group. In acyl carrier proteins (ACP) for example, it serves as a \'swinging arm\' for the attachment of activated fatty acid and amino-acid groups.
-xref: record_id "49"
-xref: delta_mono_mass "340.085794"
-xref: delta_avge_mass "340.333"
-xref: delta_composition "H(21) C(11) N(2) O(6) P S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-16 16:00:24"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:50
-name: FAD
-def: "Flavin adenine dinucleotide." [RESID:AA0143, URL:http\://www.aw-bc.com/mathews/EF/FAD.GIF, RESID:AA0144, RESID:AA0145, RESID:AA0221, FindMod:FAD, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=50]
-xref: record_id "50"
-xref: delta_mono_mass "783.141486"
-xref: delta_avge_mass "783.5339"
-xref: delta_composition "H(31) C(27) N(9) O(15) P(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-16 17:16:18"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:51
-name: Tripalmitate
-def: "N-acyl diglyceride cysteine." [PMID:10356335, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=51]
-xref: record_id "51"
-xref: delta_mono_mass "788.725777"
-xref: delta_avge_mass "789.3049"
-xref: delta_composition "H(96) C(51) O(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-18 11:47:54"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Protein N-term"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:52
-name: Guanidinyl
-def: "Guanidination." [PMID:11821862, URL:http\://www.indiana.edu/~reillyjp/ASMS2001posters/beardsley_poster.pdf, PMID:11078590, PMID:11085420, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=52]
-comment: Specific for sidechain of lysine. Does not modify the N-termini except for glycine at a slower rate than the side chain of lysine.
-synonym: "homoarginine" RELATED []
-xref: record_id "52"
-xref: delta_mono_mass "42.021798"
-xref: delta_avge_mass "42.04"
-xref: delta_composition "H(2) C N(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2011-11-21 13:56:40"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:53
-name: HNE
-def: "4-hydroxynonenal (HNE)." [PMID:11327326, PMID:15276160, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=53]
-comment: A lipid-type modification. HNE forms a Michael addition product on Cysteine, Histidine and Lysines. Unusually, it doesn\'t replace a hydrogen on the amino acid side chain.
-xref: record_id "53"
-xref: delta_mono_mass "156.11503"
-xref: delta_avge_mass "156.2221"
-xref: delta_composition "H(16) C(9) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2024-06-27 09:30:34"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "A"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Post-translational"
-xref: spec_4_misc_notes "GFAP from human brain tissues"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "L"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Post-translational"
-xref: spec_5_misc_notes "GFAP from human brain tissues"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "R"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:54
-name: Glucuronyl
-def: "Hexuronic acid." [PMID:7398618, RESID:AA0291, RESID:AA0058, URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hexa=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=54]
-comment: The addition of a sugar unit to a protein amino acid, e.g. the addition of glycan chains to proteins. Addition of glucuronic acid. Observed for N-term G.
-synonym: "glucuronosyl" RELATED []
-xref: record_id "54"
-xref: delta_mono_mass "176.032088"
-xref: delta_avge_mass "176.1241"
-xref: delta_composition "HexA"
-xref: username_of_poster "jcottrell"
-xref: group_of_poster "users"
-xref: date_time_posted "2002-10-01 21:36:48"
-xref: date_time_modified "2017-11-16 14:51:01"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Protein N-term"
-xref: spec_1_classification "Other glycosylation"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_177_mono_mass "176.032088"
-xref: spec_2_neutral_loss_177_avge_mass "176.1241"
-xref: spec_2_neutral_loss_177_flag "false"
-xref: spec_2_neutral_loss_177_composition "HexA"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_177_mono_mass "176.032088"
-xref: spec_2_neutral_loss_177_avge_mass "176.1241"
-xref: spec_2_neutral_loss_177_flag "false"
-xref: spec_2_neutral_loss_177_composition "HexA"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:55
-name: Glutathione
-def: "Glutathione disulfide." [PMID:3083866, PMID:8344916, RESID:AA0229, FindMod:GLUT, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=55]
-xref: record_id "55"
-xref: delta_mono_mass "305.068156"
-xref: delta_avge_mass "305.3076"
-xref: delta_composition "H(15) C(10) N(3) O(6) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-10-03 09:10:19"
-xref: date_time_modified "2006-10-16 15:51:52"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:56
-name: Acetyl:2H(3)
-def: "Acetate labeling reagent (N-term & K) (heavy form, +3amu)." [PMID:11857757, PMID:11999733, PMID:12175151, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=56]
-synonym: "N-trideuteriumacetoxy" RELATED []
-xref: record_id "56"
-xref: delta_mono_mass "45.029395"
-xref: delta_avge_mass "45.0552"
-xref: delta_composition "H(-1) 2H(3) C(2) O"
-xref: username_of_poster "penner"
-xref: group_of_poster "users"
-xref: date_time_posted "2002-10-16 16:41:56"
-xref: date_time_modified "2021-12-07 13:53:57"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "H"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "S"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "T"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Isotopic label"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "Y"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Isotopic label"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "N-term"
-xref: spec_7_position "Protein N-term"
-xref: spec_7_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:58
-name: Propionyl
-def: "Propionate labeling reagent light form (N-term & K)." [PMID:12175151, PMID:11999733, PMID:11857757, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=58]
-xref: record_id "58"
-xref: delta_mono_mass "56.026215"
-xref: delta_avge_mass "56.0633"
-xref: delta_composition "H(4) C(3) O"
-xref: username_of_poster "penner"
-xref: group_of_poster "users"
-xref: date_time_posted "2002-10-16 16:52:38"
-xref: date_time_modified "2021-12-07 13:54:44"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "S"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "T"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "N-term"
-xref: spec_5_position "Protein N-term"
-xref: spec_5_classification "Multiple"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:59
-name: Propionyl:13C(3)
-def: "Propionate labeling reagent heavy form (+3amu), N-term & K." [PMID:11999733, PMID:12175151, PMID:11857757, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=59]
-xref: record_id "59"
-xref: delta_mono_mass "59.036279"
-xref: delta_avge_mass "59.0412"
-xref: delta_composition "H(4) 13C(3) O"
-xref: username_of_poster "penner"
-xref: group_of_poster "users"
-xref: date_time_posted "2002-10-16 16:55:47"
-xref: date_time_modified "2021-12-07 13:55:08"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:60
-name: GIST-Quat
-def: "Quaternary amine labeling reagent light form (N-term & K)." [PMID:11857757, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=60]
-synonym: "N-(4-trimethylammoniumbutanoxy)-NHS" RELATED []
-xref: record_id "60"
-xref: delta_mono_mass "127.099714"
-xref: delta_avge_mass "127.1842"
-xref: delta_composition "H(13) C(7) N O"
-xref: username_of_poster "penner"
-xref: group_of_poster "users"
-xref: date_time_posted "2002-10-16 17:02:37"
-xref: date_time_modified "2021-12-07 13:56:41"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_neutral_loss_60_mono_mass "59.073499"
-xref: spec_1_neutral_loss_60_avge_mass "59.1103"
-xref: spec_1_neutral_loss_60_flag "false"
-xref: spec_1_neutral_loss_60_composition "H(9) C(3) N"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_2_neutral_loss_60_mono_mass "59.073499"
-xref: spec_2_neutral_loss_60_avge_mass "59.1103"
-xref: spec_2_neutral_loss_60_flag "false"
-xref: spec_2_neutral_loss_60_composition "H(9) C(3) N"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:61
-name: GIST-Quat:2H(3)
-def: "Quaternary amine labeling reagent heavy (+3amu) form, N-term & K." [PMID:11857757, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=61]
-xref: record_id "61"
-xref: delta_mono_mass "130.118544"
-xref: delta_avge_mass "130.2027"
-xref: delta_composition "H(10) 2H(3) C(7) N O"
-xref: username_of_poster "penner"
-xref: group_of_poster "users"
-xref: date_time_posted "2002-10-16 17:09:34"
-xref: date_time_modified "2021-12-07 13:57:03"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_neutral_loss_63_mono_mass "62.09233"
-xref: spec_1_neutral_loss_63_avge_mass "62.1287"
-xref: spec_1_neutral_loss_63_flag "false"
-xref: spec_1_neutral_loss_63_composition "H(6) 2H(3) C(3) N"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_2_neutral_loss_63_mono_mass "62.09233"
-xref: spec_2_neutral_loss_63_avge_mass "62.1287"
-xref: spec_2_neutral_loss_63_flag "false"
-xref: spec_2_neutral_loss_63_composition "H(6) 2H(3) C(3) N"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:62
-name: GIST-Quat:2H(6)
-def: "Quaternary amine labeling reagent heavy form (+6amu), N-term & K." [PMID:11857757, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=62]
-xref: record_id "62"
-xref: delta_mono_mass "133.137375"
-xref: delta_avge_mass "133.2212"
-xref: delta_composition "H(7) 2H(6) C(7) N O"
-xref: username_of_poster "penner"
-xref: group_of_poster "users"
-xref: date_time_posted "2002-10-16 17:12:27"
-xref: date_time_modified "2021-12-07 13:57:16"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_neutral_loss_66_mono_mass "65.11116"
-xref: spec_1_neutral_loss_66_avge_mass "65.1472"
-xref: spec_1_neutral_loss_66_flag "false"
-xref: spec_1_neutral_loss_66_composition "H(3) 2H(6) C(3) N"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_2_neutral_loss_66_mono_mass "65.11116"
-xref: spec_2_neutral_loss_66_avge_mass "65.1472"
-xref: spec_2_neutral_loss_66_flag "false"
-xref: spec_2_neutral_loss_66_composition "H(3) 2H(6) C(3) N"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:63
-name: GIST-Quat:2H(9)
-def: "Quaternary amine labeling reagent heavy form (+9amu), N-term & K." [PMID:11857757, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=63]
-xref: record_id "63"
-xref: delta_mono_mass "136.156205"
-xref: delta_avge_mass "136.2397"
-xref: delta_composition "H(4) 2H(9) C(7) N O"
-xref: username_of_poster "penner"
-xref: group_of_poster "users"
-xref: date_time_posted "2002-10-16 17:14:22"
-xref: date_time_modified "2021-12-07 13:57:28"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_neutral_loss_69_mono_mass "68.12999"
-xref: spec_1_neutral_loss_69_avge_mass "68.1657"
-xref: spec_1_neutral_loss_69_flag "false"
-xref: spec_1_neutral_loss_69_composition "2H(9) C(3) N"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_2_neutral_loss_69_mono_mass "68.12999"
-xref: spec_2_neutral_loss_69_avge_mass "68.1657"
-xref: spec_2_neutral_loss_69_flag "false"
-xref: spec_2_neutral_loss_69_composition "2H(9) C(3) N"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:64
-name: Succinyl
-def: "Succinic anhydride labeling reagent light form (N-term & K)." [RESID:AA0130, PMID:11857757, PMID:12175151, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=64]
-xref: record_id "64"
-xref: delta_mono_mass "100.016044"
-xref: delta_avge_mass "100.0728"
-xref: delta_composition "H(4) C(4) O(3)"
-xref: username_of_poster "penner"
-xref: group_of_poster "users"
-xref: date_time_posted "2002-10-16 17:17:07"
-xref: date_time_modified "2021-12-07 13:55:39"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:65
-name: Succinyl:2H(4)
-def: "Succinic anhydride labeling reagent, heavy form (+4amu, 4H2), N-term & K." [PMID:12175151, PMID:11857757, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=65]
-xref: record_id "65"
-xref: delta_mono_mass "104.041151"
-xref: delta_avge_mass "104.0974"
-xref: delta_composition "2H(4) C(4) O(3)"
-xref: username_of_poster "penner"
-xref: group_of_poster "users"
-xref: date_time_posted "2002-10-16 17:19:51"
-xref: date_time_modified "2021-12-07 13:56:27"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:66
-name: Succinyl:13C(4)
-def: "Succinic anhydride labeling reagent, heavy form (+4amu, 4C13), N-term & K." [PMID:12175151, PMID:11857757, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=66]
-xref: record_id "66"
-xref: delta_mono_mass "104.029463"
-xref: delta_avge_mass "104.0434"
-xref: delta_composition "H(4) 13C(4) O(3)"
-xref: username_of_poster "penner"
-xref: group_of_poster "users"
-xref: date_time_posted "2002-10-16 17:23:58"
-xref: date_time_modified "2021-12-07 13:56:08"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:89
-name: Iminobiotin
-def: "Iminobiotinylation." [PMID:9750125, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=89]
-xref: record_id "89"
-xref: delta_mono_mass "225.093583"
-xref: delta_avge_mass "225.3106"
-xref: delta_composition "H(15) C(10) N(3) O S"
-xref: username_of_poster "toppolzer"
-xref: group_of_poster "users"
-xref: date_time_posted "2002-11-25 16:01:48"
-xref: date_time_modified "2006-10-16 15:26:37"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:90
-name: ESP
-def: "ESP-Tag light d0." [URL:http\://www.wzw.tum.de/proteomik/forum2003/Posters-Abstracts.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=90]
-xref: record_id "90"
-xref: delta_mono_mass "338.177647"
-xref: delta_avge_mass "338.4682"
-xref: delta_composition "H(26) C(16) N(4) O(2) S"
-xref: username_of_poster "toppolzer"
-xref: group_of_poster "users"
-xref: date_time_posted "2002-11-25 16:12:50"
-xref: date_time_modified "2006-10-16 15:58:19"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:91
-name: ESP:2H(10)
-def: "ESP-Tag heavy d10." [URL:http\://www.wzw.tum.de/proteomik/forum2003/Posters-Abstracts.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=91]
-xref: record_id "91"
-xref: delta_mono_mass "348.240414"
-xref: delta_avge_mass "348.5299"
-xref: delta_composition "H(16) 2H(10) C(16) N(4) O(2) S"
-xref: username_of_poster "toppolzer"
-xref: group_of_poster "users"
-xref: date_time_posted "2002-11-25 16:18:58"
-xref: date_time_modified "2006-10-16 16:03:06"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:92
-name: NHS-LC-Biotin
-def: "NHS-LC-Biotin." [URL:http\://pubs.acs.org/doi/abs/10.1021/bi062142x, URL:http\://www.piercenet.com/Proteomics/browse.cfm?fldID=84EBE112-F871-4CA5-807F-47327153CFCB, URL:http\://www.piercenet.com/Products/Browse.cfm?fldID=8D38BA83-EFDC-421A-853F-E96EBA380612, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=92]
-synonym: "N-biotinyl-6-aminohexanoyl" RELATED []
-xref: record_id "92"
-xref: delta_mono_mass "339.161662"
-xref: delta_avge_mass "339.453"
-xref: delta_composition "H(25) C(16) N(3) O(3) S"
-xref: username_of_poster "toppolzer"
-xref: group_of_poster "users"
-xref: date_time_posted "2002-12-04 09:55:19"
-xref: date_time_modified "2015-05-07 10:57:59"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:93
-name: EDT-maleimide-PEO-biotin
-def: "EDT-maleimide-PEO-biotin." [URL:http\://www.piercenet.com/Products/Browse.cfm?fldID=01031005, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=93]
-xref: record_id "93"
-xref: delta_mono_mass "601.206246"
-xref: delta_avge_mass "601.8021"
-xref: delta_composition "H(39) C(25) N(5) O(6) S(3)"
-xref: username_of_poster "take"
-xref: group_of_poster "users"
-xref: date_time_posted "2002-12-27 09:08:56"
-xref: date_time_modified "2006-11-14 11:15:06"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:94
-name: IMID
-def: "IMID d0." [PMID:11746907, URL:http\://www.chem.agilent.com/cag/lystag.asp, URL:http\://www.chem.agilent.com/cag/other/IMTHUPO2003.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=94]
-synonym: "2-methoxy-4,5-dihydro-1H-imidazole derivative Lys imidazole" RELATED []
-xref: record_id "94"
-xref: delta_mono_mass "68.037448"
-xref: delta_avge_mass "68.0773"
-xref: delta_composition "H(4) C(3) N(2)"
-xref: username_of_poster "Liao"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-01-09 04:14:06"
-xref: date_time_modified "2006-10-16 10:33:45"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:95
-name: IMID:2H(4)
-def: "IMID d4." [URL:http\://www.chem.agilent.com/cag/lystag.asp, PMID:11746907, URL:http\://www.chem.agilent.com/cag/other/IMTHUPO2003.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=95]
-synonym: "2-methoxy-4,5-dihydro-1H-imidazole derivative" RELATED []
-xref: record_id "95"
-xref: delta_mono_mass "72.062555"
-xref: delta_avge_mass "72.1019"
-xref: delta_composition "2H(4) C(3) N(2)"
-xref: username_of_poster "Liao"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-01-09 04:15:25"
-xref: date_time_modified "2006-10-16 11:06:13"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:97
-name: Propionamide:2H(3)
-def: "Acrylamide d3." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=97]
-xref: record_id "97"
-xref: delta_mono_mass "74.055944"
-xref: delta_avge_mass "74.0964"
-xref: delta_composition "H(2) 2H(3) C(3) N O"
-xref: username_of_poster "Liao"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-01-14 08:10:30"
-xref: date_time_modified "2006-10-16 11:07:07"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:105
-name: ICAT-C
-def: "Applied Biosystems cleavable ICAT(TM) light." [URL:http\://www.chemsoc.org/exemplarchem/entries/2002/proteomics/icat.htm, URL:https\://products.appliedbiosystems.com/ab/en/US/adirect/ab?cmd=catNavigate2&catID=600902, URL:http\://docs.appliedbiosystems.com/pebiodocs/04333373.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=105]
-xref: record_id "105"
-xref: delta_mono_mass "227.126991"
-xref: delta_avge_mass "227.2603"
-xref: delta_composition "H(17) C(10) N(3) O(3)"
-xref: username_of_poster "tpjd2"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-01-27 10:27:11"
-xref: date_time_modified "2006-10-16 15:32:17"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:106
-name: ICAT-C:13C(9)
-def: "Applied Biosystems cleavable ICAT(TM) heavy." [URL:http\://docs.appliedbiosystems.com/pebiodocs/04333373.pdf, URL:https\://products.appliedbiosystems.com/ab/en/US/adirect/ab?cmd=catNavigate2&catID=600902, URL:http\://www.chemsoc.org/exemplarchem/entries/2002/proteomics/icat.htm, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=106]
-xref: record_id "106"
-xref: delta_mono_mass "236.157185"
-xref: delta_avge_mass "236.1942"
-xref: delta_composition "H(17) C 13C(9) N(3) O(3)"
-xref: username_of_poster "tpjd2"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-01-27 10:32:53"
-xref: date_time_modified "2006-10-16 15:34:14"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:107
-name: FormylMet
-def: "Addition of N-formyl met." [RESID:AA0021, PMID:10825024, PMID:8758896, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=107]
-xref: record_id "107"
-xref: delta_mono_mass "159.035399"
-xref: delta_avge_mass "159.2062"
-xref: delta_composition "H(9) C(6) N O(2) S"
-xref: username_of_poster "jphilip"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-01-27 18:24:14"
-xref: date_time_modified "2006-10-16 14:08:15"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Protein N-term"
-xref: spec_1_classification "Pre-translational"
-xref: spec_1_misc_notes "only with Listeria monocytogenes (gram-positive bacteria)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:108
-name: Nethylmaleimide
-def: "N-ethylmaleimide on cysteines." [URL:http\://www.chemistry.ucsc.edu/~fink/231/Image118.gif, PMID:12777388, PMID:11813307, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=108]
-synonym: "CysNEM" RELATED []
-xref: record_id "108"
-xref: delta_mono_mass "125.047679"
-xref: delta_avge_mass "125.1253"
-xref: delta_composition "H(7) C(6) N O(2)"
-xref: username_of_poster "Pflieger"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-01-30 09:52:51"
-xref: date_time_modified "2006-10-16 13:36:10"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:112
-name: OxLysBiotinRed
-def: "Oxidized lysine biotinylated with biotin-LC-hydrazide, reduced." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=112]
-xref: record_id "112"
-xref: delta_mono_mass "354.172562"
-xref: delta_avge_mass "354.4676"
-xref: delta_composition "H(26) C(16) N(4) O(3) S"
-xref: username_of_poster "S_Lee"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-02-21 00:53:43"
-xref: date_time_modified "2006-11-14 12:10:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:113
-name: OxLysBiotin
-def: "Oxidized lysine biotinylated with biotin-LC-hydrazide." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=113]
-xref: record_id "113"
-xref: delta_mono_mass "352.156911"
-xref: delta_avge_mass "352.4518"
-xref: delta_composition "H(24) C(16) N(4) O(3) S"
-xref: username_of_poster "S_Lee"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-02-21 01:25:11"
-xref: date_time_modified "2006-11-14 12:10:53"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:114
-name: OxProBiotinRed
-def: "Oxidized proline biotinylated with biotin-LC-hydrazide, reduced." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=114]
-xref: record_id "114"
-xref: delta_mono_mass "371.199111"
-xref: delta_avge_mass "371.4982"
-xref: delta_composition "H(29) C(16) N(5) O(3) S"
-xref: username_of_poster "S_Lee"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-02-21 01:34:28"
-xref: date_time_modified "2006-11-14 12:11:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:115
-name: OxProBiotin
-def: "Oxidized Proline biotinylated with biotin-LC-hydrazide." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=115]
-xref: record_id "115"
-xref: delta_mono_mass "369.183461"
-xref: delta_avge_mass "369.4823"
-xref: delta_composition "H(27) C(16) N(5) O(3) S"
-xref: username_of_poster "S_Lee"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-02-21 01:35:44"
-xref: date_time_modified "2006-11-14 12:11:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:116
-name: OxArgBiotin
-def: "Oxidized arginine biotinylated with biotin-LC-hydrazide." [URL:http\://www.piercenet.com/Proteomics/browse.cfm?fldID=84EBE112-F871-4CA5-807F-47327153CFCB, URL:http\://themedicalbiochemistrypage.org/nitrogen-metabolism.html, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=116]
-xref: record_id "116"
-xref: delta_mono_mass "310.135113"
-xref: delta_avge_mass "310.4118"
-xref: delta_composition "H(22) C(15) N(2) O(3) S"
-xref: username_of_poster "S_Lee"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-02-21 01:41:19"
-xref: date_time_modified "2011-07-18 11:34:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:117
-name: OxArgBiotinRed
-def: "Oxidized arginine biotinylated with biotin-LC-hydrazide, reduced." [URL:http\://www.piercenet.com/Proteomics/browse.cfm?fldID=84EBE112-F871-4CA5-807F-47327153CFCB, URL:http\://themedicalbiochemistrypage.org/nitrogen-metabolism.html, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=117]
-xref: record_id "117"
-xref: delta_mono_mass "312.150763"
-xref: delta_avge_mass "312.4277"
-xref: delta_composition "H(24) C(15) N(2) O(3) S"
-xref: username_of_poster "S_Lee"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-02-21 01:43:00"
-xref: date_time_modified "2011-07-18 11:33:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:118
-name: EDT-iodoacetyl-PEO-biotin
-def: "EDT-iodo-PEO-biotin." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=118]
-xref: record_id "118"
-xref: delta_mono_mass "490.174218"
-xref: delta_avge_mass "490.7034"
-xref: delta_composition "H(34) C(20) N(4) O(4) S(3)"
-xref: username_of_poster "take"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-02-24 07:18:42"
-xref: date_time_modified "2006-10-16 17:01:15"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:119
-name: IBTP
-def: "Thio Ether Formation - BTP Adduct." [PMID:11861642, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=119]
-xref: record_id "119"
-xref: delta_mono_mass "316.138088"
-xref: delta_avge_mass "316.3759"
-xref: delta_composition "H(21) C(22) P"
-xref: username_of_poster "MRCDunn"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-03-13 09:36:40"
-xref: date_time_modified "2006-10-16 15:52:42"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:121
-name: GG
-def: "Ubiquitinylation residue." [PMID:34673284, URL:http\://www.nottingham.ac.uk/biochemcourses/students/ub/ubindex.html, PMID:15055197, PMID:24782567, PMID:28884683, PMID:12872131, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=121]
-comment: The two glycine residues left on ubiquitinylated lysine after tryptic digestion.
-synonym: "SUMOylation leaving GG tag glycineglycine" RELATED []
-xref: record_id "121"
-xref: delta_mono_mass "114.042927"
-xref: delta_avge_mass "114.1026"
-xref: delta_composition "H(6) C(4) N(2) O(2)"
-xref: username_of_poster "gielbert"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-04-30 13:32:37"
-xref: date_time_modified "2023-09-27 10:44:25"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Other"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Other"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "C"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Other"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "N-term"
-xref: spec_5_position "Protein N-term"
-xref: spec_5_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:122
-name: Formyl
-def: "Formylation." [RESID:AA0211, PMID:15799070, RESID:AA0021, FindMod:FORM, RESID:AA0384, RESID:AA0057, RESID:AA0384, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=122]
-xref: record_id "122"
-xref: delta_mono_mass "27.994915"
-xref: delta_avge_mass "28.0101"
-xref: delta_composition "C O"
-xref: username_of_poster "pnacman"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-05-01 13:28:36"
-xref: date_time_modified "2006-11-14 12:01:57"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_misc_notes "Can occur under CNBr cleavage conditions (70% HCOOH)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Artefact"
-xref: spec_2_misc_notes "Can occur under CNBr cleavage conditions (70% HCOOH)"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "S"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Artefact"
-xref: spec_3_misc_notes "Can occur under CNBr cleavage conditions (70% HCOOH)"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "T"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Artefact"
-xref: spec_4_misc_notes "Can occur under CNBr cleavage conditions (70% HCOOH)"
-xref: spec_5_group "5"
-xref: spec_5_hidden "0"
-xref: spec_5_site "N-term"
-xref: spec_5_position "Protein N-term"
-xref: spec_5_classification "Post-translational"
-xref: spec_5_misc_notes "A protein in which either the N-terminal N-formylmethionine has not been processed by the methionyl-tRNA formyltransferase or which is posttranslationally modified by the attachment of at least one formyl group."
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:123
-name: ICAT-H
-def: "N-iodoacetyl, p-chlorobenzyl-12C6-glucamine." [PMID:12185208, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=123]
-synonym: "Harbury glyco-ICAT C12" RELATED []
-xref: record_id "123"
-xref: delta_mono_mass "345.097915"
-xref: delta_avge_mass "345.7754"
-xref: delta_composition "H(20) C(15) N O(6) Cl"
-xref: username_of_poster "allis"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-05-07 19:54:20"
-xref: date_time_modified "2006-10-16 16:02:00"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:124
-name: ICAT-H:13C(6)
-def: "N-iodoacetyl, p-chlorobenzyl-13C6-glucamine." [PMID:12185208, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=124]
-synonym: "Harbury glyco-ICAT C13" RELATED []
-xref: record_id "124"
-xref: delta_mono_mass "351.118044"
-xref: delta_avge_mass "351.7313"
-xref: delta_composition "H(20) C(9) 13C(6) N O(6) Cl"
-xref: username_of_poster "allis"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-05-07 19:56:12"
-xref: date_time_modified "2006-10-16 16:04:02"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:126
-name: Xlink:DTSSP[88]
-def: "Cleaved and reduced DSP/DTSSP crosslinker." [URL:https\://tools.thermofisher.com/content/sfs/manuals/MAN0011280_DTSSP_DSP_UG.pdf, PMID:322714, PMID:3155470, PMID:957432, PMID:8457554, PMID:11710128, PMID:1262347, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=126]
-comment: Can also be the product of reaction with EZ-Link Sulfo-NHS-SS-Biotin (Sulfosuccinimidyl 2-(biotinamido)-ethyl-1, 3-dithiopropionate) followed by reduction with DTT.
-synonym: "(Was Thioacyl)" RELATED []
-xref: record_id "126"
-xref: delta_mono_mass "87.998285"
-xref: delta_avge_mass "88.1283"
-xref: delta_composition "H(4) C(3) O S"
-xref: username_of_poster "rabah"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-06-05 13:38:19"
-xref: date_time_modified "2017-08-18 17:03:05"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:127
-name: Fluoro
-def: "Fluorination." [PMID:1093385, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=127]
-xref: record_id "127"
-xref: delta_mono_mass "17.990578"
-xref: delta_avge_mass "17.9905"
-xref: delta_composition "H(-1) F"
-xref: username_of_poster "jschulte"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-06-19 19:54:25"
-xref: date_time_modified "2012-11-20 11:56:44"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Non-standard residue"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "W"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Non-standard residue"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Non-standard residue"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "A"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:128
-name: Fluorescein
-def: "5-Iodoacetamidofluorescein (Molecular Probe, Eugene, OR)." [PMID:3578767, PMID:3311742, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=128]
-xref: record_id "128"
-xref: delta_mono_mass "387.074287"
-xref: delta_avge_mass "387.3417"
-xref: delta_composition "H(13) C(22) N O(6)"
-xref: username_of_poster "Philip"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-06-25 02:58:18"
-xref: date_time_modified "2017-11-01 12:11:48"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:129
-name: Iodo
-def: "Iodination." [PMID:2026710, PMID:15627961, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=129]
-xref: record_id "129"
-xref: delta_mono_mass "125.896648"
-xref: delta_avge_mass "125.8965"
-xref: delta_composition "H(-1) I"
-xref: username_of_poster "brettsp"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-07-10 15:43:17"
-xref: date_time_modified "2006-10-16 13:38:03"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:130
-name: Diiodo
-def: "Di-Iodination." [PMID:15627961, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=130]
-xref: record_id "130"
-xref: delta_mono_mass "251.793296"
-xref: delta_avge_mass "251.7931"
-xref: delta_composition "H(-2) I(2)"
-xref: username_of_poster "brettsp"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-07-10 15:49:42"
-xref: date_time_modified "2011-11-21 13:23:20"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:131
-name: Triiodo
-def: "Tri-Iodination." [PMID:2026710, PMID:15627961, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=131]
-xref: record_id "131"
-xref: delta_mono_mass "377.689944"
-xref: delta_avge_mass "377.6896"
-xref: delta_composition "H(-3) I(3)"
-xref: username_of_poster "brettsp"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-07-10 15:51:32"
-xref: date_time_modified "2006-10-16 16:36:49"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:134
-name: Myristoleyl
-def: "(cis-delta 5)-tetradecaenoyl." [PMID:1326520, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=134]
-comment: Found on vision signal transduction proteins.
-synonym: "myristoyl with one double bond C14:1 acylation" RELATED []
-xref: record_id "134"
-xref: delta_mono_mass "208.182715"
-xref: delta_avge_mass "208.3398"
-xref: delta_composition "H(24) C(14) O"
-xref: username_of_poster "tomneubert"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-07-18 21:30:51"
-xref: date_time_modified "2006-10-16 15:11:18"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Protein N-term"
-xref: spec_1_classification "Co-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:135
-name: Myristoyl+Delta:H(-4)
-def: "(cis,cis-delta 5, delta 8)-tetradecadienoyl." [PMID:1326520, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=135]
-comment: Found on vision signal transduction proteins.
-synonym: "myristoyl with 2 double bonds C14:2 fatty acylation" RELATED []
-xref: record_id "135"
-xref: delta_mono_mass "206.167065"
-xref: delta_avge_mass "206.3239"
-xref: delta_composition "H(22) C(14) O"
-xref: username_of_poster "tomneubert"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-07-18 21:36:44"
-xref: date_time_modified "2006-10-16 15:10:51"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Protein N-term"
-xref: spec_1_classification "Co-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:136
-name: Benzoyl
-def: "Labeling reagent light form (N-term & K)." [PMID:15456300, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=136]
-xref: record_id "136"
-xref: delta_mono_mass "104.026215"
-xref: delta_avge_mass "104.1061"
-xref: delta_composition "H(4) C(7) O"
-xref: username_of_poster "samirjulka"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-07-31 22:24:05"
-xref: date_time_modified "2006-10-16 12:41:22"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:137
-name: Hex(5)HexNAc(2)
-def: "M5/Man5." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=5&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=137]
-comment: Core structure of high-mannose N-linked oligosaccharides.
-synonym: "N-linked glycan core" RELATED []
-xref: record_id "137"
-xref: delta_mono_mass "1216.422863"
-xref: delta_avge_mass "1217.088"
-xref: delta_composition "Hex(5) HexNAc(2)"
-xref: username_of_poster "tpjd2"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-08-06 11:31:37"
-xref: date_time_modified "2020-08-02 11:50:32"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1217_mono_mass "1216.422863"
-xref: spec_1_neutral_loss_1217_avge_mass "1217.088"
-xref: spec_1_neutral_loss_1217_flag "false"
-xref: spec_1_neutral_loss_1217_composition "Hex(5) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:139
-name: Dansyl
-def: "5-dimethylaminonaphthalene-1-sulfonyl." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=139]
-xref: record_id "139"
-xref: delta_mono_mass "233.051049"
-xref: delta_avge_mass "233.2862"
-xref: delta_composition "H(11) C(12) N O(2) S"
-xref: username_of_poster "allis"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-08-19 02:51:24"
-xref: date_time_modified "2006-10-16 15:36:09"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:140
-name: a-type-ion
-def: "ISD a-series (C-Term)." [PMID:14588022, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=140]
-comment: MS/MS experiments of mass spectrometric a-ions (MS^3) can be used for protein identification by library searching. T3-sequencing is such a technique (see reference). Search engines must recognize this \'virtual modification\' for this purpose.
-synonym: "Decarboxylation of C-terminus as reaction inside the mass spectrometer" RELATED []
-xref: record_id "140"
-xref: delta_mono_mass "-46.005479"
-xref: delta_avge_mass "-46.0254"
-xref: delta_composition "H(-2) C(-1) O(-2)"
-xref: username_of_poster "suckau"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-09-02 16:17:09"
-xref: date_time_modified "2010-06-08 14:19:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Any C-term"
-xref: spec_1_classification "Other"
-xref: spec_1_misc_notes "Virtual Modification for MS/MS of a-type ions corrected by subtraction of a further -O at 8.6.2010"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:141
-name: Amidine
-def: "Amidination of lysines or N-terminal amines with methyl acetimidate." [URL:http\://www.indiana.edu/~reillyjp/ASMS2004/janecki_Ext-Abs%20Amidination.pdf, PMID:12643539, PMID:6273432, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=141]
-xref: record_id "141"
-xref: delta_mono_mass "41.026549"
-xref: delta_avge_mass "41.0519"
-xref: delta_composition "H(3) C(2) N"
-xref: username_of_poster "pnacman"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-09-25 11:04:41"
-xref: date_time_modified "2006-10-15 18:32:25"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:142
-name: HexNAc(1)dHex(1)
-def: "HexNAc1dHex1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=142]
-xref: record_id "142"
-xref: delta_mono_mass "349.137281"
-xref: delta_avge_mass "349.3337"
-xref: delta_composition "dHex HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:28:45"
-xref: date_time_modified "2015-05-05 10:49:49"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_350_mono_mass "349.137281"
-xref: spec_1_neutral_loss_350_avge_mass "349.3337"
-xref: spec_1_neutral_loss_350_flag "false"
-xref: spec_1_neutral_loss_350_composition "dHex HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_350_mono_mass "349.137281"
-xref: spec_2_neutral_loss_350_avge_mass "349.3337"
-xref: spec_2_neutral_loss_350_flag "false"
-xref: spec_2_neutral_loss_350_composition "dHex HexNAc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_350_mono_mass "349.137281"
-xref: spec_2_neutral_loss_350_avge_mass "349.3337"
-xref: spec_2_neutral_loss_350_flag "false"
-xref: spec_2_neutral_loss_350_composition "dHex HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:143
-name: HexNAc(2)
-def: "HexNAc2." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=143]
-xref: record_id "143"
-xref: delta_mono_mass "406.158745"
-xref: delta_avge_mass "406.385"
-xref: delta_composition "HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:37:55"
-xref: date_time_modified "2015-05-05 10:50:08"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_407_mono_mass "406.158745"
-xref: spec_1_neutral_loss_407_avge_mass "406.385"
-xref: spec_1_neutral_loss_407_flag "false"
-xref: spec_1_neutral_loss_407_composition "HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_407_mono_mass "406.158745"
-xref: spec_2_neutral_loss_407_avge_mass "406.385"
-xref: spec_2_neutral_loss_407_flag "false"
-xref: spec_2_neutral_loss_407_composition "HexNAc(2)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_407_mono_mass "406.158745"
-xref: spec_2_neutral_loss_407_avge_mass "406.385"
-xref: spec_2_neutral_loss_407_flag "false"
-xref: spec_2_neutral_loss_407_composition "HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:144
-name: Hex(3)
-def: "Hex3." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=144]
-xref: record_id "144"
-xref: delta_mono_mass "486.158471"
-xref: delta_avge_mass "486.4218"
-xref: delta_composition "Hex(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:39:30"
-xref: date_time_modified "2015-05-05 10:52:04"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_487_mono_mass "486.158471"
-xref: spec_1_neutral_loss_487_avge_mass "486.4218"
-xref: spec_1_neutral_loss_487_flag "false"
-xref: spec_1_neutral_loss_487_composition "Hex(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_487_mono_mass "486.158471"
-xref: spec_2_neutral_loss_487_avge_mass "486.4218"
-xref: spec_2_neutral_loss_487_flag "false"
-xref: spec_2_neutral_loss_487_composition "Hex(3)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_487_mono_mass "486.158471"
-xref: spec_2_neutral_loss_487_avge_mass "486.4218"
-xref: spec_2_neutral_loss_487_flag "false"
-xref: spec_2_neutral_loss_487_composition "Hex(3)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:145
-name: HexNAc(1)dHex(2)
-def: "HexNAc1dHex2." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=145]
-xref: record_id "145"
-xref: delta_mono_mass "495.19519"
-xref: delta_avge_mass "495.4749"
-xref: delta_composition "dHex(2) HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:40:57"
-xref: date_time_modified "2015-05-01 15:19:51"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_496_mono_mass "495.19519"
-xref: spec_1_neutral_loss_496_avge_mass "495.4749"
-xref: spec_1_neutral_loss_496_flag "false"
-xref: spec_1_neutral_loss_496_composition "dHex(2) HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:146
-name: Hex(1)HexNAc(1)dHex(1)
-def: "Hex1HexNAc1dHex1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=146]
-xref: record_id "146"
-xref: delta_mono_mass "511.190105"
-xref: delta_avge_mass "511.4743"
-xref: delta_composition "dHex Hex HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:42:27"
-xref: date_time_modified "2015-05-05 10:52:59"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_512_mono_mass "511.190105"
-xref: spec_1_neutral_loss_512_avge_mass "511.4743"
-xref: spec_1_neutral_loss_512_flag "false"
-xref: spec_1_neutral_loss_512_composition "dHex Hex HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_512_mono_mass "511.190105"
-xref: spec_2_neutral_loss_512_avge_mass "511.4743"
-xref: spec_2_neutral_loss_512_flag "false"
-xref: spec_2_neutral_loss_512_composition "dHex Hex HexNAc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_512_mono_mass "511.190105"
-xref: spec_2_neutral_loss_512_avge_mass "511.4743"
-xref: spec_2_neutral_loss_512_flag "false"
-xref: spec_2_neutral_loss_512_composition "dHex Hex HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:147
-name: HexNAc(2)dHex(1)
-def: "HexNAc2dHex1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=147]
-xref: record_id "147"
-xref: delta_mono_mass "552.216654"
-xref: delta_avge_mass "552.5262"
-xref: delta_composition "dHex HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:44:18"
-xref: date_time_modified "2015-05-01 15:23:32"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_553_mono_mass "552.216654"
-xref: spec_1_neutral_loss_553_avge_mass "552.5262"
-xref: spec_1_neutral_loss_553_flag "false"
-xref: spec_1_neutral_loss_553_composition "dHex HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:148
-name: Hex(1)HexNAc(2)
-def: "Hex1HexNAc2." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=148]
-xref: record_id "148"
-xref: delta_mono_mass "568.211569"
-xref: delta_avge_mass "568.5256"
-xref: delta_composition "Hex HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:48:18"
-xref: date_time_modified "2015-05-05 10:46:08"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_569_mono_mass "568.211569"
-xref: spec_1_neutral_loss_569_avge_mass "568.5256"
-xref: spec_1_neutral_loss_569_flag "false"
-xref: spec_1_neutral_loss_569_composition "Hex HexNAc(2)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_569_mono_mass "568.211569"
-xref: spec_2_neutral_loss_569_avge_mass "568.5256"
-xref: spec_2_neutral_loss_569_flag "false"
-xref: spec_2_neutral_loss_569_composition "Hex HexNAc(2)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_569_mono_mass "568.211569"
-xref: spec_2_neutral_loss_569_avge_mass "568.5256"
-xref: spec_2_neutral_loss_569_flag "false"
-xref: spec_2_neutral_loss_569_composition "Hex HexNAc(2)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:149
-name: Hex(1)HexNAc(1)NeuAc(1)
-def: "Hex1HexNAc1NeuAc1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=1&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=149]
-xref: record_id "149"
-xref: delta_mono_mass "656.227613"
-xref: delta_avge_mass "656.5877"
-xref: delta_composition "Hex HexNAc NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:51:19"
-xref: date_time_modified "2015-05-01 15:25:10"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_657_mono_mass "656.227613"
-xref: spec_1_neutral_loss_657_avge_mass "656.5877"
-xref: spec_1_neutral_loss_657_flag "false"
-xref: spec_1_neutral_loss_657_composition "Hex HexNAc NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_657_mono_mass "656.227613"
-xref: spec_2_neutral_loss_657_avge_mass "656.5877"
-xref: spec_2_neutral_loss_657_flag "false"
-xref: spec_2_neutral_loss_657_composition "Hex HexNAc NeuAc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_657_mono_mass "656.227613"
-xref: spec_2_neutral_loss_657_avge_mass "656.5877"
-xref: spec_2_neutral_loss_657_flag "false"
-xref: spec_2_neutral_loss_657_composition "Hex HexNAc NeuAc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:150
-name: HexNAc(2)dHex(2)
-def: "HexNAc2dHex2." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=150]
-xref: record_id "150"
-xref: delta_mono_mass "698.274563"
-xref: delta_avge_mass "698.6674"
-xref: delta_composition "dHex(2) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:52:36"
-xref: date_time_modified "2015-05-01 15:25:48"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_699_mono_mass "698.274563"
-xref: spec_1_neutral_loss_699_avge_mass "698.6674"
-xref: spec_1_neutral_loss_699_flag "false"
-xref: spec_1_neutral_loss_699_composition "dHex(2) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:151
-name: Hex(1)HexNAc(2)Pent(1)
-def: "Hex1HexNAc2Pent1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?pent=1&hex=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=151]
-xref: record_id "151"
-xref: delta_mono_mass "700.253828"
-xref: delta_avge_mass "700.6403"
-xref: delta_composition "Pent Hex HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:53:29"
-xref: date_time_modified "2015-05-01 15:26:17"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_701_mono_mass "700.253828"
-xref: spec_1_neutral_loss_701_avge_mass "700.6403"
-xref: spec_1_neutral_loss_701_flag "false"
-xref: spec_1_neutral_loss_701_composition "Pent Hex HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:152
-name: Hex(1)HexNAc(2)dHex(1)
-def: "Hex1HexNAc2dHex1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=152]
-xref: record_id "152"
-xref: delta_mono_mass "714.269478"
-xref: delta_avge_mass "714.6668"
-xref: delta_composition "dHex Hex HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:54:18"
-xref: date_time_modified "2015-05-05 16:20:33"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_715_mono_mass "714.269478"
-xref: spec_1_neutral_loss_715_avge_mass "714.6668"
-xref: spec_1_neutral_loss_715_flag "false"
-xref: spec_1_neutral_loss_715_composition "dHex Hex HexNAc(2)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_715_mono_mass "714.269478"
-xref: spec_2_neutral_loss_715_avge_mass "714.6668"
-xref: spec_2_neutral_loss_715_flag "false"
-xref: spec_2_neutral_loss_715_composition "dHex Hex HexNAc(2)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_715_mono_mass "714.269478"
-xref: spec_2_neutral_loss_715_avge_mass "714.6668"
-xref: spec_2_neutral_loss_715_flag "false"
-xref: spec_2_neutral_loss_715_composition "dHex Hex HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:153
-name: Hex(2)HexNAc(2)
-def: "Hex2HexNAc2." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=153]
-xref: record_id "153"
-xref: delta_mono_mass "730.264392"
-xref: delta_avge_mass "730.6662"
-xref: delta_composition "Hex(2) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:55:08"
-xref: date_time_modified "2015-05-05 16:22:13"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_731_mono_mass "730.264392"
-xref: spec_1_neutral_loss_731_avge_mass "730.6662"
-xref: spec_1_neutral_loss_731_flag "false"
-xref: spec_1_neutral_loss_731_composition "Hex(2) HexNAc(2)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_731_mono_mass "730.264392"
-xref: spec_2_neutral_loss_731_avge_mass "730.6662"
-xref: spec_2_neutral_loss_731_flag "false"
-xref: spec_2_neutral_loss_731_composition "Hex(2) HexNAc(2)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_731_mono_mass "730.264392"
-xref: spec_2_neutral_loss_731_avge_mass "730.6662"
-xref: spec_2_neutral_loss_731_flag "false"
-xref: spec_2_neutral_loss_731_composition "Hex(2) HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:154
-name: Hex(3)HexNAc(1)Pent(1)
-def: "Hex3HexNAc1Pent1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?pent=1&hex=3&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=154]
-xref: record_id "154"
-xref: delta_mono_mass "821.280102"
-xref: delta_avge_mass "821.7289"
-xref: delta_composition "Pent Hex(3) HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:56:02"
-xref: date_time_modified "2015-05-01 15:29:31"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_822_mono_mass "821.280102"
-xref: spec_1_neutral_loss_822_avge_mass "821.7289"
-xref: spec_1_neutral_loss_822_flag "false"
-xref: spec_1_neutral_loss_822_composition "Pent Hex(3) HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:155
-name: Hex(1)HexNAc(2)dHex(1)Pent(1)
-def: "Hex1HexNAc2dHex1Pent1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?pent=1&dhex=1&hex=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=155]
-xref: record_id "155"
-xref: delta_mono_mass "846.311736"
-xref: delta_avge_mass "846.7815"
-xref: delta_composition "Pent dHex Hex HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:57:01"
-xref: date_time_modified "2015-05-01 15:29:55"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_847_mono_mass "846.311736"
-xref: spec_1_neutral_loss_847_avge_mass "846.7815"
-xref: spec_1_neutral_loss_847_flag "false"
-xref: spec_1_neutral_loss_847_composition "Pent dHex Hex HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:156
-name: Hex(1)HexNAc(2)dHex(2)
-def: "Hex1HexNAc2dHex2." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=156]
-xref: record_id "156"
-xref: delta_mono_mass "860.327386"
-xref: delta_avge_mass "860.808"
-xref: delta_composition "dHex(2) Hex HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:57:52"
-xref: date_time_modified "2015-05-05 16:24:22"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_861_mono_mass "860.327386"
-xref: spec_1_neutral_loss_861_avge_mass "860.808"
-xref: spec_1_neutral_loss_861_flag "false"
-xref: spec_1_neutral_loss_861_composition "dHex(2) Hex HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_861_mono_mass "860.327386"
-xref: spec_2_neutral_loss_861_avge_mass "860.808"
-xref: spec_2_neutral_loss_861_flag "false"
-xref: spec_2_neutral_loss_861_composition "dHex(2) Hex HexNAc(2)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_861_mono_mass "860.327386"
-xref: spec_2_neutral_loss_861_avge_mass "860.808"
-xref: spec_2_neutral_loss_861_flag "false"
-xref: spec_2_neutral_loss_861_composition "dHex(2) Hex HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:157
-name: Hex(2)HexNAc(2)Pent(1)
-def: "Hex2HexNAc2Pent1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?pent=1&hex=2&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=157]
-xref: record_id "157"
-xref: delta_mono_mass "862.306651"
-xref: delta_avge_mass "862.7809"
-xref: delta_composition "Pent Hex(2) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:58:38"
-xref: date_time_modified "2015-05-01 15:30:54"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_863_mono_mass "862.306651"
-xref: spec_1_neutral_loss_863_avge_mass "862.7809"
-xref: spec_1_neutral_loss_863_flag "false"
-xref: spec_1_neutral_loss_863_composition "Pent Hex(2) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:158
-name: Hex(2)HexNAc(2)dHex(1)
-def: "Hex2HexNAc2dHex1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=2&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=158]
-xref: record_id "158"
-xref: delta_mono_mass "876.322301"
-xref: delta_avge_mass "876.8074"
-xref: delta_composition "dHex Hex(2) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:59:18"
-xref: date_time_modified "2015-05-05 16:26:14"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_877_mono_mass "876.322301"
-xref: spec_1_neutral_loss_877_avge_mass "876.8074"
-xref: spec_1_neutral_loss_877_flag "false"
-xref: spec_1_neutral_loss_877_composition "dHex Hex(2) HexNAc(2)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_877_mono_mass "876.322301"
-xref: spec_2_neutral_loss_877_avge_mass "876.8074"
-xref: spec_2_neutral_loss_877_flag "false"
-xref: spec_2_neutral_loss_877_composition "dHex Hex(2) HexNAc(2)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_877_mono_mass "876.322301"
-xref: spec_2_neutral_loss_877_avge_mass "876.8074"
-xref: spec_2_neutral_loss_877_flag "false"
-xref: spec_2_neutral_loss_877_composition "dHex Hex(2) HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:159
-name: Hex(3)HexNAc(2)
-def: "M3/Man3." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=159]
-synonym: "chitobiose core" RELATED []
-xref: record_id "159"
-xref: delta_mono_mass "892.317216"
-xref: delta_avge_mass "892.8068"
-xref: delta_composition "Hex(3) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:59:59"
-xref: date_time_modified "2020-08-02 11:51:23"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_893_mono_mass "892.317216"
-xref: spec_1_neutral_loss_893_avge_mass "892.8068"
-xref: spec_1_neutral_loss_893_flag "false"
-xref: spec_1_neutral_loss_893_composition "Hex(3) HexNAc(2)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_893_mono_mass "892.317216"
-xref: spec_2_neutral_loss_893_avge_mass "892.8068"
-xref: spec_2_neutral_loss_893_flag "false"
-xref: spec_2_neutral_loss_893_composition "Hex(3) HexNAc(2)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_893_mono_mass "892.317216"
-xref: spec_2_neutral_loss_893_avge_mass "892.8068"
-xref: spec_2_neutral_loss_893_flag "false"
-xref: spec_2_neutral_loss_893_composition "Hex(3) HexNAc(2)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:160
-name: Hex(1)HexNAc(1)NeuAc(2)
-def: "Hex HexNAc NeuAc(2) ---OR--- Hex HexNAc(3) HexA." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=1&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=160]
-xref: record_id "160"
-xref: delta_mono_mass "947.323029"
-xref: delta_avge_mass "947.8423"
-xref: delta_composition "Hex HexNAc NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 13:01:06"
-xref: date_time_modified "2017-11-17 11:43:49"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_948_mono_mass "947.323029"
-xref: spec_1_neutral_loss_948_avge_mass "947.8423"
-xref: spec_1_neutral_loss_948_flag "false"
-xref: spec_1_neutral_loss_948_composition "Hex HexNAc NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_948_mono_mass "947.323029"
-xref: spec_2_neutral_loss_948_avge_mass "947.8423"
-xref: spec_2_neutral_loss_948_flag "false"
-xref: spec_2_neutral_loss_948_composition "Hex HexNAc NeuAc(2)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_948_mono_mass "947.323029"
-xref: spec_2_neutral_loss_948_avge_mass "947.8423"
-xref: spec_2_neutral_loss_948_flag "false"
-xref: spec_2_neutral_loss_948_composition "Hex HexNAc NeuAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:161
-name: Hex(3)HexNAc(2)Phos(1)
-def: "Hex(3) HexNAc(2) Phos." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=1&hex=3&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=161]
-xref: record_id "161"
-xref: delta_mono_mass "972.283547"
-xref: delta_avge_mass "972.7867"
-xref: delta_composition "H O(3) P Hex(3) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 13:02:02"
-xref: date_time_modified "2015-05-06 09:48:32"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_973_mono_mass "972.283547"
-xref: spec_1_neutral_loss_973_avge_mass "972.7867"
-xref: spec_1_neutral_loss_973_flag "false"
-xref: spec_1_neutral_loss_973_composition "H O(3) P Hex(3) HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:162
-name: Delta:S(-1)Se(1)
-def: "Selenium replaces sulfur." [RESID:AA0022, PMID:12148805, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=162]
-xref: record_id "162"
-xref: delta_mono_mass "47.944449"
-xref: delta_avge_mass "46.895"
-xref: delta_composition "S(-1) Se"
-xref: username_of_poster "pnacman"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-10-14 11:24:28"
-xref: date_time_modified "2012-03-09 11:23:23"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Non-standard residue"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Non-standard residue"
-xref: spec_2_misc_notes "Selenocysteine conventionally represented by 1 letter code U"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:170
-name: Delta:H(-1)N(-1)18O(1)
-def: "Glycosylated asparagine 18O labeling." [PMID:1443554, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=170]
-comment: Conversion of glycosylated asparagine residues upon deglycosylation with PGNase F in 18O labelled water.
-xref: record_id "170"
-xref: delta_mono_mass "2.988261"
-xref: delta_avge_mass "2.9845"
-xref: delta_composition "H(-1) N(-1) 18O"
-xref: username_of_poster "lobvi"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-12-11 18:24:58"
-xref: date_time_modified "2021-05-18 09:38:20"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:171
-name: NBS:13C(6)
-def: "Shimadzu NBS-13C." [PMID:12845591, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=171]
-synonym: "NBS reagent heavy" RELATED []
-xref: record_id "171"
-xref: delta_mono_mass "159.008578"
-xref: delta_avge_mass "159.1144"
-xref: delta_composition "H(3) 13C(6) N O(2) S"
-xref: username_of_poster "kuyama"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-01-07 07:22:34"
-xref: date_time_modified "2007-08-31 10:35:22"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:172
-name: NBS
-def: "Shimadzu NBS-12C." [PMID:12845591, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=172]
-synonym: "2-nitrobenzenesulfenyl" RELATED []
-xref: record_id "172"
-xref: delta_mono_mass "152.988449"
-xref: delta_avge_mass "153.1585"
-xref: delta_composition "H(3) C(6) N O(2) S"
-xref: username_of_poster "kuyama"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-01-07 07:25:07"
-xref: date_time_modified "2007-08-31 10:34:53"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:176
-name: BHT
-def: "Michael addition of BHT quinone methide to Cysteine and Lysine." [PMID:9448752, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=176]
-comment: BHT metabolism has been studied in rats and mice in relation to tumor promotion.
-synonym: "Butylated Hydroxytoluene" RELATED []
-xref: record_id "176"
-xref: delta_mono_mass "218.167065"
-xref: delta_avge_mass "218.3346"
-xref: delta_composition "H(22) C(15) O"
-xref: username_of_poster "gonzo"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-02-05 22:02:53"
-xref: date_time_modified "2006-10-16 15:19:41"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_1_misc_notes "Secondary adduct - much less common as C"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Other"
-xref: spec_2_misc_notes "Secondary adduct - much less common as C"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "C"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Other"
-xref: spec_3_misc_notes "Primary adduct formed"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:178
-name: DAET
-def: "Phosphorylation to amine thiol." [PMID:12216740, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=178]
-comment: DAET = 2-(dimethylamino)ethanethiol; The phosphorylation to amine is the beta elimination of phosphate and Michael addition of 2-(dimethylamino)ethanethiol to the site.
-synonym: "b-elimination thiol derivatization" RELATED []
-xref: record_id "178"
-xref: delta_mono_mass "87.050655"
-xref: delta_avge_mass "87.1866"
-xref: delta_composition "H(9) C(4) N O(-1) S"
-xref: username_of_poster "chemgirl18"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-02-11 20:34:16"
-xref: date_time_modified "2006-10-16 12:34:48"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:184
-name: Label:13C(9)
-def: "13C(9) Silac label." [URL:http\://www.pil.sdu.dk/silac_intro.htm, PMID:12716131, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=184]
-synonym: "heavy tyrosine" RELATED []
-xref: record_id "184"
-xref: delta_mono_mass "9.030193"
-xref: delta_avge_mass "8.9339"
-xref: delta_composition "C(-9) 13C(9)"
-xref: username_of_poster "hs"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-02-16 21:19:47"
-xref: date_time_modified "2007-08-22 18:31:52"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "Used in SILAC experiment"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "F"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:185
-name: Label:13C(9)+Phospho
-def: "C13 label (Phosphotyrosine)." [PMID:12716131, URL:http\://www.pil.sdu.dk/silac_intro.htm, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=185]
-synonym: "heavy phosphotyrosine" RELATED []
-xref: record_id "185"
-xref: delta_mono_mass "88.996524"
-xref: delta_avge_mass "88.9138"
-xref: delta_composition "H C(-9) 13C(9) O(3) P"
-xref: username_of_poster "hs"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-02-22 04:42:33"
-xref: date_time_modified "2006-10-16 12:37:51"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "Used in SILAC experiment"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:186
-name: HPG
-def: "Hydroxyphenylglyoxal arginine." [PMID:11698400, PMID:11914093, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=186]
-synonym: "HPG arginine" RELATED []
-xref: record_id "186"
-xref: delta_mono_mass "132.021129"
-xref: delta_avge_mass "132.1162"
-xref: delta_composition "H(4) C(8) O(2)"
-xref: username_of_poster "gcarven"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-02-26 20:19:25"
-xref: date_time_modified "2006-10-17 11:46:39"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:187
-name: 2HPG
-def: "Bis(hydroxphenylglyoxal) arginine." [PMID:11698400, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=187]
-comment: OH-PGO and PGO react with arginine at a stoichiometry of 2:1.
-xref: record_id "187"
-xref: delta_mono_mass "282.052824"
-xref: delta_avge_mass "282.2476"
-xref: delta_composition "H(10) C(16) O(5)"
-xref: username_of_poster "gcarven"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-02-26 22:05:25"
-xref: date_time_modified "2009-06-26 17:37:17"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:188
-name: Label:13C(6)
-def: "13C(6) Silac label." [URL:http\://www.pil.sdu.dk/silac_intro.htm, PMID:12716131, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=188]
-xref: record_id "188"
-xref: delta_mono_mass "6.020129"
-xref: delta_avge_mass "5.9559"
-xref: delta_composition "C(-6) 13C(6)"
-xref: username_of_poster "hs"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-02-28 19:54:10"
-xref: date_time_modified "2007-08-22 18:29:56"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "Used in SILAC experiment"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-xref: spec_2_misc_notes "Used in SILAC experiment"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "L"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Used in SILAC experiment"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "I"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Isotopic label"
-xref: spec_5_misc_notes "Used in SILAC experiment"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:193
-name: Label:18O(2)
-def: "O18 label at both C-terminal oxygens." [PMID:11467524, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=193]
-synonym: "Double O18 (C-term)" RELATED []
-xref: record_id "193"
-xref: delta_mono_mass "4.008491"
-xref: delta_avge_mass "3.9995"
-xref: delta_composition "O(-2) 18O(2)"
-xref: username_of_poster "Hensbergen"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-03-30 14:20:29"
-xref: date_time_modified "2006-11-14 12:01:04"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Any C-term"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:194
-name: AccQTag
-def: "6-aminoquinolyl-N-hydroxysuccinimidyl carbamate." [URL:http\://www2.waters.com/watprod.nsf/newdocs/930494, PMID:14997490, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=194]
-xref: record_id "194"
-xref: delta_mono_mass "170.048013"
-xref: delta_avge_mass "170.1674"
-xref: delta_composition "H(6) C(10) N(2) O"
-xref: username_of_poster "davidcreasy"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-04-08 12:01:19"
-xref: date_time_modified "2006-10-16 14:59:12"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:195
-name: QAT
-def: "APTA-d0." [PMID:15283597, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=195]
-synonym: "(3-acrylamidopropyl)trimethylammonium" RELATED []
-xref: record_id "195"
-xref: delta_mono_mass "171.149738"
-xref: delta_avge_mass "171.26"
-xref: delta_composition "H(19) C(9) N(2) O"
-xref: username_of_poster "s_julka"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-04-08 17:12:14"
-xref: date_time_modified "2009-06-26 17:39:29"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:196
-name: QAT:2H(3)
-def: "APTA d3." [PMID:15283597, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=196]
-synonym: "(3-acrylamidopropyl)trimethylammonium" RELATED []
-xref: record_id "196"
-xref: delta_mono_mass "174.168569"
-xref: delta_avge_mass "174.2784"
-xref: delta_composition "H(16) 2H(3) C(9) N(2) O"
-xref: username_of_poster "s_julka"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-04-08 17:15:04"
-xref: date_time_modified "2006-10-16 15:01:35"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:197
-name: EQAT
-def: "EAPTA d0." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=197]
-xref: record_id "197"
-xref: delta_mono_mass "184.157563"
-xref: delta_avge_mass "184.2786"
-xref: delta_composition "H(20) C(10) N(2) O"
-xref: username_of_poster "s_julka"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-04-08 17:21:08"
-xref: date_time_modified "2006-10-16 15:05:02"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:198
-name: EQAT:2H(5)
-def: "EAPTA d5." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=198]
-xref: record_id "198"
-xref: delta_mono_mass "189.188947"
-xref: delta_avge_mass "189.3094"
-xref: delta_composition "H(15) 2H(5) C(10) N(2) O"
-xref: username_of_poster "s_julka"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-04-08 17:25:24"
-xref: date_time_modified "2006-10-16 15:07:31"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:199
-name: Dimethyl:2H(4)
-def: "DiMethyl-CHD2." [PMID:14670044, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=199]
-synonym: "reductive amination" RELATED []
-xref: record_id "199"
-xref: delta_mono_mass "32.056407"
-xref: delta_avge_mass "32.0778"
-xref: delta_composition "2H(4) C(2)"
-xref: username_of_poster "PhilipHsu"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-04-20 07:07:29"
-xref: date_time_modified "2014-11-16 07:35:30"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "When dimethyl labelling is pre-digest"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "R"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:200
-name: Ethanedithiol
-def: "EDT." [PMID:11507762, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=200]
-xref: record_id "200"
-xref: delta_mono_mass "75.980527"
-xref: delta_avge_mass "76.1838"
-xref: delta_composition "H(4) C(2) O(-1) S(2)"
-xref: username_of_poster "take"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-04-20 08:27:30"
-xref: date_time_modified "2006-10-16 11:07:38"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:205
-name: Delta:H(6)C(6)O(1)
-def: "Acrolein addition +94." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=205]
-synonym: "Acrolein94, FDP" RELATED []
-xref: record_id "205"
-xref: delta_mono_mass "94.041865"
-xref: delta_avge_mass "94.1112"
-xref: delta_composition "H(6) C(6) O"
-xref: username_of_poster "fatcat"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-05-06 18:54:17"
-xref: date_time_modified "2006-10-16 12:38:28"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:206
-name: Delta:H(4)C(3)O(1)
-def: "Acrolein addition +56." [PMID:15541752, PMID:10825247, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=206]
-synonym: "Acrolein56" RELATED []
-xref: record_id "206"
-xref: delta_mono_mass "56.026215"
-xref: delta_avge_mass "56.0633"
-xref: delta_composition "H(4) C(3) O"
-xref: username_of_poster "fatcat"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-05-06 18:55:58"
-xref: date_time_modified "2017-11-08 16:29:48"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Other"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Other"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "R"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:207
-name: Delta:H(2)C(3)
-def: "Acrolein addition +38." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=207]
-synonym: "Acrolein38" RELATED []
-xref: record_id "207"
-xref: delta_mono_mass "38.01565"
-xref: delta_avge_mass "38.048"
-xref: delta_composition "H(2) C(3)"
-xref: username_of_poster "fatcat"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-05-06 18:57:08"
-xref: date_time_modified "2006-10-15 18:30:31"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:208
-name: Delta:H(4)C(6)
-def: "Acrolein addition +76." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=208]
-synonym: "Acrolein76" RELATED []
-xref: record_id "208"
-xref: delta_mono_mass "76.0313"
-xref: delta_avge_mass "76.096"
-xref: delta_composition "H(4) C(6)"
-xref: username_of_poster "fatcat"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-05-06 18:59:23"
-xref: date_time_modified "2006-10-16 11:08:13"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:209
-name: Delta:H(8)C(6)O(2)
-def: "Acrolein addition +112." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=209]
-synonym: "Acrolein112" RELATED []
-xref: record_id "209"
-xref: delta_mono_mass "112.05243"
-xref: delta_avge_mass "112.1265"
-xref: delta_composition "H(8) C(6) O(2)"
-xref: username_of_poster "fatcat"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-05-06 19:00:25"
-xref: date_time_modified "2006-10-16 12:46:03"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:211
-name: NEIAA
-def: "N-ethyl iodoacetamide-d0." [PMID:12766232, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=211]
-xref: record_id "211"
-xref: delta_mono_mass "85.052764"
-xref: delta_avge_mass "85.1045"
-xref: delta_composition "H(7) C(4) N O"
-xref: username_of_poster "Botting"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-05-18 11:10:37"
-xref: date_time_modified "2006-10-16 12:15:11"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "Y"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:212
-name: NEIAA:2H(5)
-def: "N-ethyl iodoacetamide-d5." [PMID:12766232, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=212]
-xref: record_id "212"
-xref: delta_mono_mass "90.084148"
-xref: delta_avge_mass "90.1353"
-xref: delta_composition "H(2) 2H(5) C(4) N O"
-xref: username_of_poster "Botting"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-05-18 11:11:52"
-xref: date_time_modified "2006-10-16 12:38:09"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "Y"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:213
-name: ADP-Ribosyl
-def: "ADP Ribose addition." [URL:http\://betelgeuse.u-strasbg.fr/DocPARP/DocPARG/images/Structure-pADPR.jpg, PMID:15842200, RESID:AA0231, RESID:AA0237, RESID:AA0295, FindMod:ADP, RESID:AA0168, RESID:AA0169, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=213]
-xref: record_id "213"
-xref: delta_mono_mass "541.06111"
-xref: delta_avge_mass "541.3005"
-xref: delta_composition "H(13) C(10) N(5) O(9) P(2) Pent"
-xref: username_of_poster "ionjockey"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-05-27 20:53:37"
-xref: date_time_modified "2024-08-12 09:51:41"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other glycosylation"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Other glycosylation"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "N-linked glycosylation"
-xref: spec_3_neutral_loss_0_mono_mass "0"
-xref: spec_3_neutral_loss_0_avge_mass "0"
-xref: spec_3_neutral_loss_0_flag "false"
-xref: spec_3_neutral_loss_0_composition "0"
-xref: spec_3_neutral_loss_542_mono_mass "541.06111"
-xref: spec_3_neutral_loss_542_avge_mass "541.3005"
-xref: spec_3_neutral_loss_542_flag "false"
-xref: spec_3_neutral_loss_542_composition "H(13) C(10) N(5) O(9) P(2) Pent"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "T"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "O-linked glycosylation"
-xref: spec_4_neutral_loss_542_mono_mass "541.06111"
-xref: spec_4_neutral_loss_542_avge_mass "541.3005"
-xref: spec_4_neutral_loss_542_flag "false"
-xref: spec_4_neutral_loss_542_composition "H(13) C(10) N(5) O(9) P(2) Pent"
-xref: spec_4_neutral_loss_0_mono_mass "0"
-xref: spec_4_neutral_loss_0_avge_mass "0"
-xref: spec_4_neutral_loss_0_flag "false"
-xref: spec_4_neutral_loss_0_composition "0"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "S"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "O-linked glycosylation"
-xref: spec_4_neutral_loss_0_mono_mass "0"
-xref: spec_4_neutral_loss_0_avge_mass "0"
-xref: spec_4_neutral_loss_0_flag "false"
-xref: spec_4_neutral_loss_0_composition "0"
-xref: spec_4_neutral_loss_542_mono_mass "541.06111"
-xref: spec_4_neutral_loss_542_avge_mass "541.3005"
-xref: spec_4_neutral_loss_542_flag "false"
-xref: spec_4_neutral_loss_542_composition "H(13) C(10) N(5) O(9) P(2) Pent"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "E"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Other glycosylation"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "K"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Other glycosylation"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "D"
-xref: spec_7_position "Anywhere"
-xref: spec_7_classification "Other glycosylation"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:214
-name: iTRAQ4plex
-def: "Representative mass and accurate mass for 116 & 117." [URL:http\://docs.appliedbiosystems.com/pebiodocs/04351918.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=214]
-comment: Different channels have the same nominal mass but slightly different exact masses. Use this value for all channels for quantitation purposes. mTRAQ heavy is identical to iTRAQ4plex 117.
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry AKA iTRAQ4plex116/7" RELATED []
-xref: record_id "214"
-xref: delta_mono_mass "144.102063"
-xref: delta_avge_mass "144.1544"
-xref: delta_composition "H(12) C(4) 13C(3) N 15N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2004-06-08 14:04:07"
-xref: date_time_modified "2024-08-12 09:52:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "0"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Low abundance"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "H"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "Very low abundance"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "S"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Isotopic label"
-xref: spec_5_misc_notes "Very low abundance"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "T"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Isotopic label"
-xref: spec_6_misc_notes "Very low abundance"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "N-term"
-xref: spec_7_position "Protein N-term"
-xref: spec_7_classification "Isotopic label"
-xref: spec_8_group "8"
-xref: spec_8_hidden "1"
-xref: spec_8_site "C"
-xref: spec_8_position "Anywhere"
-xref: spec_8_classification "Isotopic label"
-xref: spec_8_misc_notes "side reaction"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:243
-name: IGBP
-def: "Light IDBEST tag for quantitation." [URL:http\://www.targetdiscovery.com/index.php?topic=prod.idbe, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=243]
-xref: record_id "243"
-xref: delta_mono_mass "296.016039"
-xref: delta_avge_mass "297.1478"
-xref: delta_composition "H(13) C(12) N(2) O(2) Br"
-xref: username_of_poster "zqiao"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-07-26 23:02:04"
-xref: date_time_modified "2006-10-19 11:13:26"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:253
-name: Crotonaldehyde
-def: "Crotonaldehyde." [PMID:11283024, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=253]
-xref: record_id "253"
-xref: delta_mono_mass "70.041865"
-xref: delta_avge_mass "70.0898"
-xref: delta_composition "H(6) C(4) O"
-xref: username_of_poster "fatcat"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-08-12 19:56:03"
-xref: date_time_modified "2006-10-16 10:35:31"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Other"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:254
-name: Delta:H(2)C(2)
-def: "Acetaldehyde +26." [PMID:7744761, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=254]
-comment: Lys modification is formation of Schiff base.
-xref: record_id "254"
-xref: delta_mono_mass "26.01565"
-xref: delta_avge_mass "26.0373"
-xref: delta_composition "H(2) C(2)"
-xref: username_of_poster "fatcat"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-08-12 20:01:03"
-xref: date_time_modified "2011-11-21 13:14:17"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Other"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Other"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "N-term"
-xref: spec_4_position "Any N-term"
-xref: spec_4_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:255
-name: Delta:H(4)C(2)
-def: "Acetaldehyde +28." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=255]
-comment: Reduction of Schiff base formed between K amino group and acetaldehyde.
-xref: record_id "255"
-xref: delta_mono_mass "28.0313"
-xref: delta_avge_mass "28.0532"
-xref: delta_composition "H(4) C(2)"
-xref: username_of_poster "fatcat"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-08-12 20:02:38"
-xref: date_time_modified "2011-11-21 13:14:58"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Other"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:256
-name: Delta:H(4)C(3)
-def: "Propionaldehyde +40." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=256]
-xref: record_id "256"
-xref: delta_mono_mass "40.0313"
-xref: delta_avge_mass "40.0639"
-xref: delta_composition "H(4) C(3)"
-xref: username_of_poster "fatcat"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-08-12 20:04:01"
-xref: date_time_modified "2010-02-25 10:49:55"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Other"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:258
-name: Label:18O(1)
-def: "O18 Labeling." [PMID:11467524, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=258]
-synonym: "H2 18O Alkaline Phosphatase" RELATED []
-xref: record_id "258"
-xref: delta_mono_mass "2.004246"
-xref: delta_avge_mass "1.9998"
-xref: delta_composition "O(-1) 18O"
-xref: username_of_poster "chemgirl18"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-08-27 21:57:17"
-xref: date_time_modified "2006-10-13 18:53:41"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "alkaline phosphatase to dephosphorylate"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-xref: spec_2_misc_notes "alkaline phosphatase to dephosphorylate"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "alkaline phosphatase to dephosphorylate"
-xref: spec_4_group "4"
-xref: spec_4_hidden "0"
-xref: spec_4_site "C-term"
-xref: spec_4_position "Any C-term"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "digesting in labelled water"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:259
-name: Label:13C(6)15N(2)
-def: "13C(6) 15N(2) Silac label." [PMID:12716131, URL:http\://www.pil.sdu.dk/silac_intro.htm, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=259]
-synonym: "heavy lysine" RELATED []
-xref: record_id "259"
-xref: delta_mono_mass "8.014199"
-xref: delta_avge_mass "7.9427"
-xref: delta_composition "C(-6) 13C(6) N(-2) 15N(2)"
-xref: username_of_poster "hs01"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-08-30 16:23:02"
-xref: date_time_modified "2014-06-09 09:40:49"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "Used in SILAC experiment"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:260
-name: Thiophospho
-def: "Thiophosphorylation." [PMID:12110917, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=260]
-xref: record_id "260"
-xref: delta_mono_mass "95.943487"
-xref: delta_avge_mass "96.0455"
-xref: delta_composition "H O(2) P S"
-xref: username_of_poster "mrbladergroen"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-09-01 13:20:58"
-xref: date_time_modified "2006-10-16 12:38:48"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Other"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:261
-name: SPITC
-def: "4-sulfophenyl isothiocyanate." [URL:http\://www.shimadzu-biotech.net/literature/application_note/202_1.pdf, PMID:14745769, PMID:14689565, PMID:16526082, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=261]
-synonym: "N-terminal / lysine sulfonation" RELATED []
-xref: record_id "261"
-xref: delta_mono_mass "214.971084"
-xref: delta_avge_mass "215.2495"
-xref: delta_composition "H(5) C(7) N O(3) S(2)"
-xref: username_of_poster "hatlevig"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-09-14 20:01:29"
-xref: date_time_modified "2006-10-16 15:26:00"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:262
-name: Label:2H(3)
-def: "Trideuteration." [URL:http\://www.pil.sdu.dk/silac_intro.htm, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=262]
-synonym: "Trideuteration" RELATED []
-xref: record_id "262"
-xref: delta_mono_mass "3.01883"
-xref: delta_avge_mass "3.0185"
-xref: delta_composition "H(-3) 2H(3)"
-xref: username_of_poster "mmolloy"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-09-29 08:52:01"
-xref: date_time_modified "2013-02-22 12:42:11"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "for SILAC expt"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "M"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:264
-name: PET
-def: "Phosphorylation to pyridyl thiol." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=264]
-comment: PET = 2-[4-pyridyl]ethanethiol. This modification is a chemical derivative, based on a alkaline catalysed beta-elimination of phosphoserines and phosphothreonines and subsequent 1,4-addition of 2-[4-pyridine]ethanethiol. These modified serines and threonines produce in MS/MS a characteristic fragment which can be used for precursor-ion-scan experiments.
-synonym: "b-elimination PET derivatisation" RELATED []
-xref: record_id "264"
-xref: delta_mono_mass "121.035005"
-xref: delta_avge_mass "121.2028"
-xref: delta_composition "H(7) C(7) N O(-1) S"
-xref: username_of_poster "vbad"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-10-07 08:55:33"
-xref: date_time_modified "2006-10-16 12:48:51"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:267
-name: Label:13C(6)15N(4)
-def: "13C(6) 15N(4) Silac label." [URL:http\://www.pil.sdu.dk/silac_intro.htm, PMID:12716131, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=267]
-xref: record_id "267"
-xref: delta_mono_mass "10.008269"
-xref: delta_avge_mass "9.9296"
-xref: delta_composition "C(-6) 13C(6) N(-4) 15N(4)"
-xref: username_of_poster "AFCS"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-10-20 17:49:33"
-xref: date_time_modified "2006-10-19 10:30:51"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "Used in SILAC experiment"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:268
-name: Label:13C(5)15N(1)
-def: "13C(5) 15N(1) Silac label." [PMID:12771378, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=268]
-xref: record_id "268"
-xref: delta_mono_mass "6.013809"
-xref: delta_avge_mass "5.9567"
-xref: delta_composition "C(-5) 13C(5) N(-1) 15N"
-xref: username_of_poster "Deepa"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-11-05 18:49:37"
-xref: date_time_modified "2011-11-21 14:48:39"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "Used in AQUA experiment"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "P"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-xref: spec_2_misc_notes "Result of conversion of 13C6, 15N4 arginine to 13C5, 15N1 proline"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "M"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "SILAC label used in COFRADIC"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "E"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:269
-name: Label:13C(9)15N(1)
-def: "13C(9) 15N(1) Silac label." [URL:http\://www.pil.sdu.dk/silac_intro.htm, PMID:12771378, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=269]
-xref: record_id "269"
-xref: delta_mono_mass "10.027228"
-xref: delta_avge_mass "9.9273"
-xref: delta_composition "C(-9) 13C(9) N(-1) 15N"
-xref: username_of_poster "Deepa"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-11-05 18:51:13"
-xref: date_time_modified "2006-10-19 10:31:10"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "Used in AQUA experiment"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:270
-name: Cytopiloyne
-def: "Nucleophilic addtion to cytopiloyne." [PMID:15549660, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=270]
-comment: Cytopiloyne is a polyacetylenic glucoside isolated form Bidens pilosa which can modulate T helper cell differentiation. Biotinylated cytopiloyne might be use to identify its receptor in T cell.
-xref: record_id "270"
-xref: delta_mono_mass "362.136553"
-xref: delta_avge_mass "362.3738"
-xref: delta_composition "H(22) C(19) O(7)"
-xref: username_of_poster "ymchiang"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-11-10 03:13:23"
-xref: date_time_modified "2006-10-16 16:35:54"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "P"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "R"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "S"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "Y"
-xref: spec_7_position "Anywhere"
-xref: spec_7_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:271
-name: Cytopiloyne+water
-def: "Nucleophilic addition to cytopiloyne+H2O." [PMID:15549660, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=271]
-comment: Cytopiloyne is a polyacetylenic glucoside isolated form Bidens pilosa which can modulated T helper cell differentiation. Biotinylated cytopiloyne might be use to identify its receptor in T cell.
-xref: record_id "271"
-xref: delta_mono_mass "380.147118"
-xref: delta_avge_mass "380.3891"
-xref: delta_composition "H(24) C(19) O(8)"
-xref: username_of_poster "ymchiang"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-11-11 05:23:17"
-xref: date_time_modified "2006-10-16 16:37:10"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "R"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "S"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "T"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "Y"
-xref: spec_7_position "Anywhere"
-xref: spec_7_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:272
-name: CAF
-def: "Sulfonation of N-terminus." [PMID:15732931, PMID:16046801, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=272]
-comment: N-terminal sulfonation of diglycine to detect ubiquitination sites.
-synonym: "Ettan CAF MALDI" RELATED []
-xref: record_id "272"
-xref: delta_mono_mass "135.983029"
-xref: delta_avge_mass "136.1265"
-xref: delta_composition "H(4) C(3) O(4) S"
-xref: username_of_poster "chens002"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-11-16 14:25:33"
-xref: date_time_modified "2007-01-03 19:34:35"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:275
-name: Nitrosyl
-def: "Nitrosylation." [FindMod:NTRY, PMID:10442087, RESID:AA0230, PMID:15688001, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=275]
-xref: record_id "275"
-xref: delta_mono_mass "28.990164"
-xref: delta_avge_mass "28.9982"
-xref: delta_composition "H(-1) N O"
-xref: username_of_poster "dengh"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-12-11 00:23:12"
-xref: date_time_modified "2019-09-10 09:17:23"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_1_misc_notes "S-nitrosylation"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "Y"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_2_misc_notes "photochemical decomposition"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:276
-name: AEBS
-def: "Aminoethylbenzenesulfonylation." [PMID:8597590, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=276]
-comment: Potential protein modification when using AEBSF (Pefabloc) as a serine protease inhibitor.
-xref: record_id "276"
-xref: delta_mono_mass "183.035399"
-xref: delta_avge_mass "183.2276"
-xref: delta_composition "H(9) C(8) N O(2) S"
-xref: username_of_poster "plattm"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-12-14 04:38:25"
-xref: date_time_modified "2006-10-16 15:04:42"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Artefact"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "S"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Artefact"
-xref: spec_4_misc_notes "Primary site of modification"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "Y"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:278
-name: Ethanolyl
-def: "Ethanolation." [PMID:15351294, PMID:7730303, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=278]
-synonym: "Hydroxy ethyl" RELATED []
-xref: record_id "278"
-xref: delta_mono_mass "44.026215"
-xref: delta_avge_mass "44.0526"
-xref: delta_composition "H(4) C(2) O"
-xref: username_of_poster "knierman"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-01-11 04:26:47"
-xref: date_time_modified "2017-10-09 15:47:39"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "from reaction of SH group with iodoethanol"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_2_misc_notes "reduced form of oxidation product"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "R"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_misc_notes "reduced form of oxidation product"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:280
-name: Ethyl
-def: "Ethylation." [PMID:9629898, URL:http\://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2911956&tool=pmcentrez&rendertype=abstract, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=280]
-xref: record_id "280"
-xref: delta_mono_mass "28.0313"
-xref: delta_avge_mass "28.0532"
-xref: delta_composition "H(4) C(2)"
-xref: username_of_poster "Qishanl"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-01-27 23:18:07"
-xref: date_time_modified "2015-08-26 14:42:10"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Multiple"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Multiple"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "E"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Artefact"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "N-term"
-xref: spec_4_position "Protein N-term"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "C-term"
-xref: spec_5_position "Any C-term"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "D"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:281
-name: CoenzymeA
-def: "Cysteine modified Coenzyme A." [URL:http\://commons.wikimedia.org/wiki/Image\:Coenzyme_a.png, RESID:AA0306, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=281]
-xref: record_id "281"
-xref: delta_mono_mass "765.09956"
-xref: delta_avge_mass "765.5182"
-xref: delta_composition "H(34) C(21) N(7) O(16) P(3) S"
-xref: username_of_poster "tremis"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-02-01 17:10:00"
-xref: date_time_modified "2006-10-16 17:15:18"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:284
-name: Methyl:2H(2)
-def: "Deuterium Methylation of Lysine." [PMID:15525938, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=284]
-xref: record_id "284"
-xref: delta_mono_mass "16.028204"
-xref: delta_avge_mass "16.0389"
-xref: delta_composition "2H(2) C"
-xref: username_of_poster "Glebivanov"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-02-13 01:26:38"
-xref: date_time_modified "2016-06-14 11:53:24"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:285
-name: SulfanilicAcid
-def: "Light Sulfanilic Acid (SA) C12." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=285]
-synonym: "C-Terminal/Glutamate/Aspartate sulfonation" RELATED []
-xref: record_id "285"
-xref: delta_mono_mass "155.004099"
-xref: delta_avge_mass "155.1744"
-xref: delta_composition "H(5) C(6) N O(2) S"
-xref: username_of_poster "apanchaud"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-02-17 15:48:07"
-xref: date_time_modified "2006-10-16 14:05:34"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Any C-term"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "D"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "E"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:286
-name: SulfanilicAcid:13C(6)
-def: "Heavy Sulfanilic Acid (SA) C13." [PMID:9254591, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=286]
-synonym: "C-Terminal/Glutamate/Aspartate sulfonation" RELATED []
-xref: record_id "286"
-xref: delta_mono_mass "161.024228"
-xref: delta_avge_mass "161.1303"
-xref: delta_composition "H(5) 13C(6) N O(2) S"
-xref: username_of_poster "apanchaud"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-02-17 15:55:52"
-xref: date_time_modified "2006-10-16 14:08:42"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Any C-term"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "D"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "E"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:288
-name: Trp->Oxolactone
-def: "Tryptophan oxidation to oxolactone." [PMID:7949339, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=288]
-comment: The cleavage of a peptide bond between Try-Xxx with oxidation of tryptophan to the oxolactone occurs in the presence of BNPS-skatole. This is a useful method for the chemical cleavage of proteins specifically at tryptophan residues.
-xref: record_id "288"
-xref: delta_mono_mass "13.979265"
-xref: delta_avge_mass "13.9835"
-xref: delta_composition "H(-2) O"
-xref: username_of_poster "oxolactone"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-02-25 23:30:20"
-xref: date_time_modified "2006-10-14 10:06:01"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:289
-name: Biotin-PEO-Amine
-def: "Biotin polyethyleneoxide amine." [URL:http\://www.piercenet.com/Proteomics/browse.cfm?fldID=84EBE112-F871-4CA5-807F-47327153CFCB, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=289]
-comment: EDC crosslinker is used to couple biotin PEO-amine to carboxyl groups or 5\' phosphate groups.
-xref: record_id "289"
-xref: delta_mono_mass "356.188212"
-xref: delta_avge_mass "356.4835"
-xref: delta_composition "H(28) C(16) N(4) O(3) S"
-xref: username_of_poster "TBricker1"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-03-02 16:49:17"
-xref: date_time_modified "2006-11-14 11:15:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Protein C-term"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "EDC-coupled modification of D, E and C-terminus"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "D"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_2_misc_notes "EDC-coupled modification of D, E and C-terminus"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "E"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_misc_notes "EDC-coupled modification of D, E and C-terminus"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:290
-name: Biotin-HPDP
-def: "Pierce EZ-Link Biotin-HPDP." [URL:http\://www.piercenet.com/Products/Browse.cfm?fldID=01031002, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=290]
-xref: record_id "290"
-xref: delta_mono_mass "428.191582"
-xref: delta_avge_mass "428.6124"
-xref: delta_composition "H(32) C(19) N(4) O(3) S(2)"
-xref: username_of_poster "tgreco"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-03-03 22:56:52"
-xref: date_time_modified "2010-12-03 16:28:07"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:291
-name: Delta:Hg(1)
-def: "Mercury Mercaptan." [PMID:10695144, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=291]
-xref: record_id "291"
-xref: delta_mono_mass "201.970617"
-xref: delta_avge_mass "200.59"
-xref: delta_composition "Hg"
-xref: username_of_poster "tgreco"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-03-03 23:53:00"
-xref: date_time_modified "2006-10-16 15:09:18"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:292
-name: IodoU-AMP
-def: "(Iodo)-uracil MP." [PMID:11567090, PMID:11112526, PMID:6540775, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=292]
-comment: One note about this chemistry is that for W you have to take care of O2 big time (and extract the I-uracil monophosphate with organics to get rid of residual iodide).
-synonym: "UV induced linkage of Iodo-U-amp with WFY" RELATED []
-xref: record_id "292"
-xref: delta_mono_mass "322.020217"
-xref: delta_avge_mass "322.1654"
-xref: delta_composition "H(11) C(9) N(2) O(9) P"
-xref: username_of_poster "davidERICanderson"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-03-04 22:57:55"
-xref: date_time_modified "2017-01-31 13:36:23"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "Used in base/residue interactions (in principle?)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "W"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_2_misc_notes "Used in base/residue interactions (observed)"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_misc_notes "Used in base/residue interactions (in principle?)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:293
-name: CAMthiopropanoyl
-def: "3-(carbamidomethylthio)propanoyl." [PMID:15121203, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=293]
-synonym: "3-thiopropanoyl moiety from reduced DSP crosslinker or NHS-SS-biotin, modified with Iodoacetamide" RELATED []
-xref: record_id "293"
-xref: delta_mono_mass "145.019749"
-xref: delta_avge_mass "145.1796"
-xref: delta_composition "H(7) C(5) N O(2) S"
-xref: username_of_poster "vanschra"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-03-09 15:22:46"
-xref: date_time_modified "2006-10-16 13:58:55"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:294
-name: IED-Biotin
-def: "Biotinoyl-iodoacetyl-ethylenediamine." [PMID:10906242, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=294]
-xref: record_id "294"
-xref: delta_mono_mass "326.141261"
-xref: delta_avge_mass "326.4145"
-xref: delta_composition "H(22) C(14) N(4) O(3) S"
-xref: username_of_poster "alexey"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-03-10 16:28:09"
-xref: date_time_modified "2006-10-16 15:53:29"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:295
-name: dHex
-def: "Fucose." [PMID:15189151, PMID:11344537, URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=295]
-synonym: "deoxyhexose" RELATED []
-xref: record_id "295"
-xref: delta_mono_mass "146.057909"
-xref: delta_avge_mass "146.1412"
-xref: delta_composition "dHex"
-xref: username_of_poster "rsack"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-03-22 16:57:00"
-xref: date_time_modified "2017-11-23 11:42:26"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_147_mono_mass "146.057909"
-xref: spec_1_neutral_loss_147_avge_mass "146.1412"
-xref: spec_1_neutral_loss_147_flag "false"
-xref: spec_1_neutral_loss_147_composition "dHex"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_147_mono_mass "146.057909"
-xref: spec_1_neutral_loss_147_avge_mass "146.1412"
-xref: spec_1_neutral_loss_147_flag "false"
-xref: spec_1_neutral_loss_147_composition "dHex"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_misc_notes "Not reported for human proteins"
-xref: spec_2_neutral_loss_147_mono_mass "146.057909"
-xref: spec_2_neutral_loss_147_avge_mass "146.1412"
-xref: spec_2_neutral_loss_147_flag "false"
-xref: spec_2_neutral_loss_147_composition "dHex"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:298
-name: Methyl:2H(3)
-def: "Deuterated methyl ester." [URL:http\://www.sigmaaldrich.com/technical-documents/articles/stable-isotopes/stable-isotope-labeling-by-amino-acids.html, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=298]
-xref: record_id "298"
-xref: delta_mono_mass "17.03448"
-xref: delta_avge_mass "17.0451"
-xref: delta_composition "H(-1) 2H(3) C"
-xref: username_of_poster "ndacoyas"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-03-24 16:31:28"
-xref: date_time_modified "2013-02-07 16:43:18"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "esterification of carboxylic acids using D3-Methanolic HCl"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "D"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-xref: spec_2_misc_notes "esterification of carboxylic acids using D3-Methanolic HCl"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "E"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "esterification of carboxylic acids using D3-Methanolic HCl"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "K"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "SILAC labelling with L-Methionine-(methyl-d3)"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "R"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Isotopic label"
-xref: spec_5_misc_notes "SILAC labelling with L-Methionine-(methyl-d3)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:299
-name: Carboxy
-def: "Carboxylation." [RESID:AA0114, FindMod:GGLU, RESID:AA0363, RESID:AA0032, PMID:3802193, RESID:AA0304, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=299]
-xref: record_id "299"
-xref: delta_mono_mass "43.989829"
-xref: delta_avge_mass "44.0095"
-xref: delta_composition "C O(2)"
-xref: username_of_poster "Carol"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-03-29 22:55:44"
-xref: date_time_modified "2006-11-14 11:08:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "D"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-xref: spec_3_misc_notes "Gamma-carboxylation"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "E"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Post-translational"
-xref: spec_4_misc_notes "Gamma-carboxylation"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "M"
-xref: spec_5_position "Protein N-term"
-xref: spec_5_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:301
-name: Bromobimane
-def: "Monobromobimane derivative." [PMID:7856876, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=301]
-synonym: "mBromobimane" RELATED []
-xref: record_id "301"
-xref: delta_mono_mass "190.074228"
-xref: delta_avge_mass "190.1986"
-xref: delta_composition "H(10) C(10) N(2) O(2)"
-xref: username_of_poster "catsriku"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-04-04 23:03:13"
-xref: date_time_modified "2006-10-16 15:07:49"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:302
-name: Menadione
-def: "Menadione quinone derivative." [PMID:15939799, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=302]
-synonym: "Vitamin k3 (Q)" RELATED []
-xref: record_id "302"
-xref: delta_mono_mass "170.036779"
-xref: delta_avge_mass "170.1641"
-xref: delta_composition "H(6) C(11) O(2)"
-xref: username_of_poster "catsriku"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-04-04 23:21:29"
-xref: date_time_modified "2007-07-12 07:36:32"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:303
-name: DeStreak
-def: "Cysteine mercaptoethanol." [PMID:12442261, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=303]
-xref: record_id "303"
-xref: delta_mono_mass "75.998285"
-xref: delta_avge_mass "76.1176"
-xref: delta_composition "H(4) C(2) O S"
-xref: username_of_poster "harald"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-04-11 14:06:08"
-xref: date_time_modified "2006-10-16 11:07:55"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:305
-name: dHex(1)Hex(3)HexNAc(4)
-def: "FA2/G0F." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=305]
-xref: record_id "305"
-xref: delta_mono_mass "1444.53387"
-xref: delta_avge_mass "1445.3331"
-xref: delta_composition "dHex Hex(3) HexNAc(4)"
-xref: username_of_poster "whaskins"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-04-25 18:20:12"
-xref: date_time_modified "2020-08-02 11:42:31"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1445_mono_mass "1444.53387"
-xref: spec_1_neutral_loss_1445_avge_mass "1445.3331"
-xref: spec_1_neutral_loss_1445_flag "false"
-xref: spec_1_neutral_loss_1445_composition "dHex Hex(3) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_1445_mono_mass "1444.53387"
-xref: spec_2_neutral_loss_1445_avge_mass "1445.3331"
-xref: spec_2_neutral_loss_1445_flag "false"
-xref: spec_2_neutral_loss_1445_composition "dHex Hex(3) HexNAc(4)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_1445_mono_mass "1444.53387"
-xref: spec_2_neutral_loss_1445_avge_mass "1445.3331"
-xref: spec_2_neutral_loss_1445_flag "false"
-xref: spec_2_neutral_loss_1445_composition "dHex Hex(3) HexNAc(4)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:307
-name: dHex(1)Hex(4)HexNAc(4)
-def: "FA2G1/G1F." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=4&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=307]
-synonym: "dHex Hex(4) HexNAc(4) ---OR--- Hex(4) HexNAc(4) Pent Me" RELATED []
-xref: record_id "307"
-xref: delta_mono_mass "1606.586693"
-xref: delta_avge_mass "1607.4737"
-xref: delta_composition "dHex Hex(4) HexNAc(4)"
-xref: username_of_poster "whaskins"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-04-25 19:22:11"
-xref: date_time_modified "2020-08-02 11:55:46"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1607_mono_mass "1606.586693"
-xref: spec_1_neutral_loss_1607_avge_mass "1607.4737"
-xref: spec_1_neutral_loss_1607_flag "false"
-xref: spec_1_neutral_loss_1607_composition "dHex Hex(4) HexNAc(4)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_1607_mono_mass "1606.586693"
-xref: spec_2_neutral_loss_1607_avge_mass "1607.4737"
-xref: spec_2_neutral_loss_1607_flag "false"
-xref: spec_2_neutral_loss_1607_composition "dHex Hex(4) HexNAc(4)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_1607_mono_mass "1606.586693"
-xref: spec_2_neutral_loss_1607_avge_mass "1607.4737"
-xref: spec_2_neutral_loss_1607_flag "false"
-xref: spec_2_neutral_loss_1607_composition "dHex Hex(4) HexNAc(4)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:308
-name: dHex(1)Hex(5)HexNAc(4)
-def: "FA2G2/G2F." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=5&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=308]
-xref: record_id "308"
-xref: delta_mono_mass "1768.639517"
-xref: delta_avge_mass "1769.6143"
-xref: delta_composition "dHex Hex(5) HexNAc(4)"
-xref: username_of_poster "whaskins"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-04-25 19:25:17"
-xref: date_time_modified "2020-08-02 11:41:19"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1769_mono_mass "1768.639517"
-xref: spec_1_neutral_loss_1769_avge_mass "1769.6143"
-xref: spec_1_neutral_loss_1769_flag "false"
-xref: spec_1_neutral_loss_1769_composition "dHex Hex(5) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:309
-name: Hex(3)HexNAc(4)
-def: "A2/G0." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=309]
-xref: record_id "309"
-xref: delta_mono_mass "1298.475961"
-xref: delta_avge_mass "1299.1919"
-xref: delta_composition "Hex(3) HexNAc(4)"
-xref: username_of_poster "whaskins"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-04-25 19:27:51"
-xref: date_time_modified "2020-08-02 11:39:23"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1299_mono_mass "1298.475961"
-xref: spec_1_neutral_loss_1299_avge_mass "1299.1919"
-xref: spec_1_neutral_loss_1299_flag "false"
-xref: spec_1_neutral_loss_1299_composition "Hex(3) HexNAc(4)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_1299_mono_mass "1298.475961"
-xref: spec_2_neutral_loss_1299_avge_mass "1299.1919"
-xref: spec_2_neutral_loss_1299_flag "false"
-xref: spec_2_neutral_loss_1299_composition "Hex(3) HexNAc(4)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_1299_mono_mass "1298.475961"
-xref: spec_2_neutral_loss_1299_avge_mass "1299.1919"
-xref: spec_2_neutral_loss_1299_flag "false"
-xref: spec_2_neutral_loss_1299_composition "Hex(3) HexNAc(4)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:310
-name: Hex(4)HexNAc(4)
-def: "A2G1/G1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=310]
-xref: record_id "310"
-xref: delta_mono_mass "1460.528784"
-xref: delta_avge_mass "1461.3325"
-xref: delta_composition "Hex(4) HexNAc(4)"
-xref: username_of_poster "whaskins"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-04-25 19:33:37"
-xref: date_time_modified "2020-08-02 11:38:53"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1461_mono_mass "1460.528784"
-xref: spec_1_neutral_loss_1461_avge_mass "1461.3325"
-xref: spec_1_neutral_loss_1461_flag "false"
-xref: spec_1_neutral_loss_1461_composition "Hex(4) HexNAc(4)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_1461_mono_mass "1460.528784"
-xref: spec_2_neutral_loss_1461_avge_mass "1461.3325"
-xref: spec_2_neutral_loss_1461_flag "false"
-xref: spec_2_neutral_loss_1461_composition "Hex(4) HexNAc(4)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_1461_mono_mass "1460.528784"
-xref: spec_2_neutral_loss_1461_avge_mass "1461.3325"
-xref: spec_2_neutral_loss_1461_flag "false"
-xref: spec_2_neutral_loss_1461_composition "Hex(4) HexNAc(4)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:311
-name: Hex(5)HexNAc(4)
-def: "A2G2/G2." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=5&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=311]
-xref: record_id "311"
-xref: delta_mono_mass "1622.581608"
-xref: delta_avge_mass "1623.4731"
-xref: delta_composition "Hex(5) HexNAc(4)"
-xref: username_of_poster "whaskins"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-04-25 19:35:54"
-xref: date_time_modified "2020-08-02 11:38:17"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1623_mono_mass "1622.581608"
-xref: spec_1_neutral_loss_1623_avge_mass "1623.4731"
-xref: spec_1_neutral_loss_1623_flag "false"
-xref: spec_1_neutral_loss_1623_composition "Hex(5) HexNAc(4)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_misc_notes "Not reported for human proteins"
-xref: spec_2_neutral_loss_1623_mono_mass "1622.581608"
-xref: spec_2_neutral_loss_1623_avge_mass "1623.4731"
-xref: spec_2_neutral_loss_1623_flag "false"
-xref: spec_2_neutral_loss_1623_composition "Hex(5) HexNAc(4)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_misc_notes "Not reported for human proteins"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_1623_mono_mass "1622.581608"
-xref: spec_2_neutral_loss_1623_avge_mass "1623.4731"
-xref: spec_2_neutral_loss_1623_flag "false"
-xref: spec_2_neutral_loss_1623_composition "Hex(5) HexNAc(4)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:312
-name: Cysteinyl
-def: "Cysteinylation." [RESID:AA0025, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=312]
-xref: record_id "312"
-xref: delta_mono_mass "119.004099"
-xref: delta_avge_mass "119.1423"
-xref: delta_composition "H(5) C(3) N O(2) S"
-xref: username_of_poster "whaskins"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-04-25 19:59:43"
-xref: date_time_modified "2006-12-17 11:28:36"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Multiple"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:313
-name: Lys-loss
-def: "Loss of Lysine." [PMID:16078144, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=313]
-xref: record_id "313"
-xref: delta_mono_mass "-128.094963"
-xref: delta_avge_mass "-128.1723"
-xref: delta_composition "H(-12) C(-6) N(-2) O(-1)"
-xref: username_of_poster "whaskins"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-04-25 20:05:38"
-xref: date_time_modified "2021-09-06 11:24:44"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Protein C-term"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Artefact"
-xref: spec_2_misc_notes "Error in peptide synthesis"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:314
-name: Nmethylmaleimide
-def: "Nmethylmaleimide." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=314]
-xref: record_id "314"
-xref: delta_mono_mass "111.032028"
-xref: delta_avge_mass "111.0987"
-xref: delta_composition "H(5) C(5) N O(2)"
-xref: username_of_poster "whaskins"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-04-25 20:12:24"
-xref: date_time_modified "2006-10-16 17:26:09"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:316
-name: DimethylpyrroleAdduct
-def: "2,5-dimethypyrrole." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=316]
-xref: record_id "316"
-xref: delta_mono_mass "78.04695"
-xref: delta_avge_mass "78.1118"
-xref: delta_composition "H(6) C(6)"
-xref: username_of_poster "Qishanl"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-05-07 03:11:23"
-xref: date_time_modified "2006-10-16 11:14:22"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:318
-name: Delta:H(2)C(5)
-def: "MDA adduct +62." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=318]
-comment: Usually major adduct formed from malondialdehyde (MDA) with the amino group of lysine residues.
-synonym: "MDA62" RELATED []
-xref: record_id "318"
-xref: delta_mono_mass "62.01565"
-xref: delta_avge_mass "62.0694"
-xref: delta_composition "H(2) C(5)"
-xref: username_of_poster "rkupfer"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-05-12 22:00:21"
-xref: date_time_modified "2006-10-16 10:29:55"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:319
-name: Delta:H(2)C(3)O(1)
-def: "MDA adduct +54." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=319]
-synonym: "MDA54" RELATED []
-xref: record_id "319"
-xref: delta_mono_mass "54.010565"
-xref: delta_avge_mass "54.0474"
-xref: delta_composition "H(2) C(3) O"
-xref: username_of_poster "rkupfer"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-05-12 22:12:10"
-xref: date_time_modified "2006-10-16 10:15:34"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "Malondialdehyde (MDA) adduct"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "R"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_2_misc_notes "5-hydro-5-methylimidazol-4-one, Methylglyoxal adduct"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:320
-name: Nethylmaleimide+water
-def: "Nethylmaleimidehydrolysis." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=320]
-xref: record_id "320"
-xref: delta_mono_mass "143.058243"
-xref: delta_avge_mass "143.1406"
-xref: delta_composition "H(9) C(6) N O(3)"
-xref: username_of_poster "whaskins"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-05-16 22:18:42"
-xref: date_time_modified "2006-10-17 11:40:14"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:323
-name: Xlink:B10621
-def: "Bis-((N-iodoacetyl)piperazinyl)sulfonerhodamine." [URL:https\://www.thermofisher.com/us/en/home/references/molecular-probes-the-handbook/crosslinking-and-photoactivatable-reagents/chemical-crosslinking-reagents.html#head2, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=323]
-comment: Discontinued Invitrogen X-link reagent.
-synonym: "BSR monolink" RELATED []
-xref: record_id "323"
-xref: delta_mono_mass "713.093079"
-xref: delta_avge_mass "713.5626"
-xref: delta_composition "H(30) C(31) N(4) O(6) S I"
-xref: username_of_poster "dengh"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-05-17 22:56:12"
-xref: date_time_modified "2017-09-05 15:32:46"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:324
-name: Xlink:DTBP[87]
-def: "Cleaved and reduced DTBP crosslinker." [PMID:770170, URL:http\://tools.thermofisher.com/content/sfs/manuals/MAN0011314_ImidoesterCrsLnk_DMA_DMP_DMS_DTBP_UG.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=324]
-comment: Imidoester cross-linker.
-synonym: "dimethyl 3,3'-dithiobispropionimidate" RELATED []
-xref: record_id "324"
-xref: delta_mono_mass "87.01427"
-xref: delta_avge_mass "87.1435"
-xref: delta_composition "H(5) C(3) N S"
-xref: username_of_poster "takesin"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-05-18 08:43:26"
-xref: date_time_modified "2017-08-18 14:19:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:325
-name: FP-Biotin
-def: "10-ethoxyphosphinyl-N-(biotinamidopentyl)decanamide." [PMID:10611275, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=325]
-comment: FP-biotin was designed to label the active site serine of serine esterases/proteases.
-synonym: "O-ethyl-N-(biotinamidopentyl)decanamido phosphonate" RELATED []
-xref: record_id "325"
-xref: delta_mono_mass "572.316129"
-xref: delta_avge_mass "572.7405"
-xref: delta_composition "H(49) C(27) N(4) O(5) P S"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-05-19 22:01:37"
-xref: date_time_modified "2010-02-24 20:54:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "Y"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "K"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:327
-name: Delta:H(4)C(2)O(-1)S(1)
-def: "S-Ethylcystine from Serine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=327]
-comment: Phosphoserine to S-ethylcystine via Beta elimination/Michael addition of ethylthiol.
-xref: record_id "327"
-xref: delta_mono_mass "44.008456"
-xref: delta_avge_mass "44.1188"
-xref: delta_composition "H(4) C(2) O(-1) S"
-xref: username_of_poster "UCDMSF"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-06-20 20:09:02"
-xref: date_time_modified "2006-10-16 10:00:57"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:329
-name: Methyl:2H(3)13C(1)
-def: "Monomethylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=329]
-xref: record_id "329"
-xref: delta_mono_mass "18.037835"
-xref: delta_avge_mass "18.0377"
-xref: delta_composition "H(-1) 2H(3) 13C"
-xref: username_of_poster "sams"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-06-30 18:19:34"
-xref: date_time_modified "2016-06-14 11:54:23"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:330
-name: Dimethyl:2H(6)13C(2)
-def: "Dimethylation." [PMID:15782174, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=330]
-xref: record_id "330"
-xref: delta_mono_mass "36.07567"
-xref: delta_avge_mass "36.0754"
-xref: delta_composition "H(-2) 2H(6) 13C(2)"
-xref: username_of_poster "sams"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-06-30 18:21:32"
-xref: date_time_modified "2014-11-16 07:36:47"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Isotopic label"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "N-term"
-xref: spec_4_position "Protein N-term"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "When dimethyl labelling is pre-digest"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:332
-name: Thiophos-S-S-biotin
-def: "Thiophosphate labeled with biotin-HPDP." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=332]
-synonym: "Thiophos-biotin disulfide" RELATED []
-xref: record_id "332"
-xref: delta_mono_mass "525.142894"
-xref: delta_avge_mass "525.6658"
-xref: delta_composition "H(34) C(19) N(4) O(5) P S(3)"
-xref: username_of_poster "lparker"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-07-21 16:37:10"
-xref: date_time_modified "2006-10-16 17:02:42"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_neutral_loss_526_mono_mass "525.142894"
-xref: spec_1_neutral_loss_526_avge_mass "525.6658"
-xref: spec_1_neutral_loss_526_flag "false"
-xref: spec_1_neutral_loss_526_composition "H(34) C(19) N(4) O(5) P S(3)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_2_neutral_loss_526_mono_mass "525.142894"
-xref: spec_2_neutral_loss_526_avge_mass "525.6658"
-xref: spec_2_neutral_loss_526_flag "false"
-xref: spec_2_neutral_loss_526_composition "H(34) C(19) N(4) O(5) P S(3)"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_neutral_loss_526_mono_mass "525.142894"
-xref: spec_3_neutral_loss_526_avge_mass "525.6658"
-xref: spec_3_neutral_loss_526_flag "false"
-xref: spec_3_neutral_loss_526_composition "H(34) C(19) N(4) O(5) P S(3)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:333
-name: Can-FP-biotin
-def: "6-N-biotinylaminohexyl isopropyl phosphate." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=333]
-comment: Commercially available from Toronto Research Chemicals Inc, as of 2005. Designed to label the active site serine of serine esterases/proteases.
-synonym: "O-isopropyl-N-biotinylaminohexyl phosphonate" RELATED []
-xref: record_id "333"
-xref: delta_mono_mass "447.195679"
-xref: delta_avge_mass "447.5291"
-xref: delta_composition "H(34) C(19) N(3) O(5) P S"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-07-21 20:54:00"
-xref: date_time_modified "2010-12-03 16:24:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "Y"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:335
-name: HNE+Delta:H(2)
-def: "Reduced 4-Hydroxynonenal." [PMID:11910026, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=335]
-comment: Michael addition adduct of 4-hydroxynonenal with histidine, cystein and lysine residues stabilized by reduction with NaBH4.
-xref: record_id "335"
-xref: delta_mono_mass "158.13068"
-xref: delta_avge_mass "158.238"
-xref: delta_composition "H(18) C(9) O(2)"
-xref: username_of_poster "rkupfer"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-08-10 20:52:36"
-xref: date_time_modified "2011-07-18 11:28:34"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:337
-name: Methylamine
-def: "Michael addition with methylamine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=337]
-xref: record_id "337"
-xref: delta_mono_mass "13.031634"
-xref: delta_avge_mass "13.0418"
-xref: delta_composition "H(3) C N O(-1)"
-xref: username_of_poster "zhulx"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-08-12 21:55:51"
-xref: date_time_modified "2006-10-14 10:02:51"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:340
-name: Bromo
-def: "Bromination." [PMID:9033387, RESID:AA0174, RESID:AA0175, RESID:AA0176, RESID:AA0173, RESID:AA0180, RESID:AA0179, FindMod:BROM, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=340]
-xref: record_id "340"
-xref: delta_mono_mass "77.910511"
-xref: delta_avge_mass "78.8961"
-xref: delta_composition "H(-1) Br"
-xref: username_of_poster "gerribe"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-09-06 08:31:51"
-xref: date_time_modified "2011-11-21 12:07:51"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "F"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "Y"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:342
-name: Amino
-def: "Tyrosine oxidation to 2-aminotyrosine." [PMID:9252331, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=342]
-xref: record_id "342"
-xref: delta_mono_mass "15.010899"
-xref: delta_avge_mass "15.0146"
-xref: delta_composition "H N"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-09-10 21:18:23"
-xref: date_time_modified "2006-10-14 10:39:53"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:343
-name: Argbiotinhydrazide
-def: "Oxidized Arginine biotinylated with biotin hydrazide." [PMID:15828771, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=343]
-xref: record_id "343"
-xref: delta_mono_mass "199.066699"
-xref: delta_avge_mass "199.27"
-xref: delta_composition "H(13) C(9) N O(2) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-09-10 22:36:58"
-xref: date_time_modified "2006-11-14 12:10:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:344
-name: Arg->GluSA
-def: "Arginine oxidation to glutamic semialdehyde." [PMID:9252331, PMID:1680314, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=344]
-synonym: "Arginine oxidation to gamma-glutamyl semialdehyde" RELATED []
-xref: record_id "344"
-xref: delta_mono_mass "-43.053433"
-xref: delta_avge_mass "-43.0711"
-xref: delta_composition "H(-5) C(-1) N(-3) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-09-10 22:38:24"
-xref: date_time_modified "2006-11-16 15:25:28"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:345
-name: Trioxidation
-def: "Cysteine oxidation to cysteic acid." [PMID:14678012, PMID:9252331, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=345]
-xref: record_id "345"
-xref: delta_mono_mass "47.984744"
-xref: delta_avge_mass "47.9982"
-xref: delta_composition "O(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-09-10 22:39:38"
-xref: date_time_modified "2017-11-08 16:28:19"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "W"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "F"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:348
-name: His->Asn
-def: "His->Asn substitution." [PMID:9252331, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=348]
-synonym: "histidine oxidation to aspargine" RELATED []
-xref: record_id "348"
-xref: delta_mono_mass "-23.015984"
-xref: delta_avge_mass "-23.0366"
-xref: delta_composition "H(-1) C(-2) N(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-09-10 22:43:27"
-xref: date_time_modified "2011-06-23 12:00:22"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_1_misc_notes "Could also be classed as chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:349
-name: His->Asp
-def: "His->Asp substitution." [PMID:9252331, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=349]
-synonym: "histidine oxidation to aspartic acid" RELATED []
-xref: record_id "349"
-xref: delta_mono_mass "-22.031969"
-xref: delta_avge_mass "-22.0519"
-xref: delta_composition "H(-2) C(-2) N(-2) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-09-10 22:44:32"
-xref: date_time_modified "2011-06-23 12:00:45"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_1_misc_notes "Could also be classed as chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:350
-name: Trp->Hydroxykynurenin
-def: "Tryptophan oxidation to hydroxykynurenin." [URL:http\://www.lbqp.unb.br/bioq/htm/aulas2D/deg_aa_ile_leu_trp.htm?reload_coolmenus, PMID:9252331, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=350]
-xref: record_id "350"
-xref: delta_mono_mass "19.989829"
-xref: delta_avge_mass "19.9881"
-xref: delta_composition "C(-1) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-09-10 22:47:20"
-xref: date_time_modified "2006-11-14 17:40:45"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:351
-name: Trp->Kynurenin
-def: "Tryptophan oxidation to kynurenin." [PMID:9252331, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=351]
-xref: record_id "351"
-xref: delta_mono_mass "3.994915"
-xref: delta_avge_mass "3.9887"
-xref: delta_composition "C(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-09-10 22:48:33"
-xref: date_time_modified "2006-10-14 09:39:53"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:352
-name: Lys->Allysine
-def: "Lysine oxidation to aminoadipic semialdehyde." [RESID:AA0121, FindMod:ALLYS, PMID:9252331, PMID:11120890, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=352]
-xref: record_id "352"
-xref: delta_mono_mass "-1.031634"
-xref: delta_avge_mass "-1.0311"
-xref: delta_composition "H(-3) N(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-09-10 22:49:59"
-xref: date_time_modified "2006-10-13 18:27:28"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:353
-name: Lysbiotinhydrazide
-def: "Oxidized Lysine biotinylated with biotin hydrazide." [URL:http\://www.piercenet.com/Proteomics/browse.cfm?fldID=84EBE112-F871-4CA5-807F-47327153CFCB, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=353]
-xref: record_id "353"
-xref: delta_mono_mass "241.088497"
-xref: delta_avge_mass "241.31"
-xref: delta_composition "H(15) C(10) N(3) O(2) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-09-10 22:51:13"
-xref: date_time_modified "2006-11-14 12:12:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:354
-name: Nitro
-def: "Oxidation to nitro." [PMID:8839040, PMID:9252331, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=354]
-xref: record_id "354"
-xref: delta_mono_mass "44.985078"
-xref: delta_avge_mass "44.9976"
-xref: delta_composition "H(-1) N O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-09-10 22:52:38"
-xref: date_time_modified "2017-11-08 16:26:39"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "Y"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "F"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:357
-name: probiotinhydrazide
-def: "Oxidized proline biotinylated with biotin hydrazide." [URL:http\://www.piercenet.com/Proteomics/browse.cfm?fldID=84EBE112-F871-4CA5-807F-47327153CFCB, PMID:15174056, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=357]
-xref: record_id "357"
-xref: delta_mono_mass "258.115047"
-xref: delta_avge_mass "258.3405"
-xref: delta_composition "H(18) C(10) N(4) O(2) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-09-10 22:56:20"
-xref: date_time_modified "2006-11-14 12:12:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:359
-name: Pro->pyro-Glu
-def: "Proline oxidation to pyroglutamic acid." [PMID:9252331, PMID:10717661, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=359]
-xref: record_id "359"
-xref: delta_mono_mass "13.979265"
-xref: delta_avge_mass "13.9835"
-xref: delta_composition "H(-2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-09-10 22:58:42"
-xref: date_time_modified "2006-10-14 10:03:34"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:360
-name: Pro->Pyrrolidinone
-def: "Proline oxidation to pyrrolidinone." [PMID:9252331, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=360]
-xref: record_id "360"
-xref: delta_mono_mass "-30.010565"
-xref: delta_avge_mass "-30.026"
-xref: delta_composition "H(-2) C(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-09-10 23:00:19"
-xref: date_time_modified "2006-10-13 15:37:42"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:361
-name: Thrbiotinhydrazide
-def: "Oxidized Threonine biotinylated with biotin hydrazide." [URL:http\://www.piercenet.com/Proteomics/browse.cfm?fldID=84EBE112-F871-4CA5-807F-47327153CFCB, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=361]
-xref: record_id "361"
-xref: delta_mono_mass "240.104482"
-xref: delta_avge_mass "240.3252"
-xref: delta_composition "H(16) C(10) N(4) O S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-09-10 23:01:28"
-xref: date_time_modified "2006-11-14 12:12:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:362
-name: Diisopropylphosphate
-def: "O-Diisopropylphosphorylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=362]
-comment: A selective label for the active site serine of the serine esterase/protease family. It has also been shown to label tyrosine in serum albumin.
-xref: record_id "362"
-xref: delta_mono_mass "164.060231"
-xref: delta_avge_mass "164.1394"
-xref: delta_composition "H(13) C(6) O(3) P"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-09-14 18:05:04"
-xref: date_time_modified "2011-12-05 16:14:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "K"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "N-term"
-xref: spec_5_position "Any N-term"
-xref: spec_5_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:363
-name: Isopropylphospho
-def: "O-Isopropylphosphorylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=363]
-comment: Created by auto-catalytic dealkylation of the O-Diisopropylphosphate adduct.
-xref: record_id "363"
-xref: delta_mono_mass "122.013281"
-xref: delta_avge_mass "122.0596"
-xref: delta_composition "H(7) C(3) O(3) P"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-09-14 18:08:20"
-xref: date_time_modified "2007-01-15 15:25:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:364
-name: ICPL:13C(6)
-def: "Bruker Daltonics SERVA-ICPL(TM) quantification chemistry, heavy form." [URL:http\://www.bdal.de/life-science-tools/care-consumables-more/icpl-kit.html, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=364]
-comment: Attention: As the digest is typically applied AFTER ICPL_light/heavy labeling, only ProteinN-term labeling and Lys-specific labeling is applied.
-xref: record_id "364"
-xref: delta_mono_mass "111.041593"
-xref: delta_avge_mass "111.05"
-xref: delta_composition "H(3) 13C(6) N O"
-xref: username_of_poster "suckau"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-09-19 12:45:52"
-xref: date_time_modified "2008-09-03 15:27:07"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_2_misc_notes "Use when labelling pre-digest"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Use when labelling post-digest"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:365
-name: ICPL
-def: "Bruker Daltonics SERVA-ICPL(TM) quantification chemistry, light form." [URL:http\://www.bdal.de/life-science-tools/care-consumables-more/icpl-kit.html, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=365]
-comment: Attention: As the digest is typically applied AFTER ICPL_light/heavy labeling, only ProteinN-term labeling and Lys-specific labeling is applied.
-xref: record_id "365"
-xref: delta_mono_mass "105.021464"
-xref: delta_avge_mass "105.0941"
-xref: delta_composition "H(3) C(6) N O"
-xref: username_of_poster "suckau"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-09-19 13:00:14"
-xref: date_time_modified "2008-09-03 15:26:36"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_2_misc_notes "Use when labelling pre-digest"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Use when labelling post-digest"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:366
-name: Deamidated:18O(1)
-def: "Deamidation in presence of O18." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=366]
-comment: Observed.
-xref: record_id "366"
-xref: delta_mono_mass "2.988261"
-xref: delta_avge_mass "2.9845"
-xref: delta_composition "H(-1) N(-1) 18O"
-xref: username_of_poster "gerribe"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-09-22 15:30:16"
-xref: date_time_modified "2006-10-14 09:35:33"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:368
-name: Cys->Dha
-def: "Dehydroalanine (from Cysteine)." [PMID:11212008, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=368]
-xref: record_id "368"
-xref: delta_mono_mass "-33.987721"
-xref: delta_avge_mass "-34.0809"
-xref: delta_composition "H(-2) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-02 17:31:11"
-xref: date_time_modified "2006-10-13 15:27:46"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:369
-name: Pro->Pyrrolidone
-def: "Pyrrolidone from Proline." [PMID:9252331, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=369]
-xref: record_id "369"
-xref: delta_mono_mass "-27.994915"
-xref: delta_avge_mass "-28.0101"
-xref: delta_composition "C(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-02 17:39:05"
-xref: date_time_modified "2006-11-14 11:12:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:371
-name: HMVK
-def: "Michael addition of hydroxymethylvinyl ketone to cysteine." [PMID:11743741, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=371]
-synonym: "hydroxymethylvinyl ketone" RELATED []
-xref: record_id "371"
-xref: delta_mono_mass "86.036779"
-xref: delta_avge_mass "86.0892"
-xref: delta_composition "H(6) C(4) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-03 15:59:33"
-xref: date_time_modified "2006-10-16 12:15:35"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:372
-name: Arg->Orn
-def: "Ornithine from Arginine." [PMID:15489230, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=372]
-xref: record_id "372"
-xref: delta_mono_mass "-42.021798"
-xref: delta_avge_mass "-42.04"
-xref: delta_composition "H(-2) C(-1) N(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-05 17:55:25"
-xref: date_time_modified "2006-10-13 15:26:33"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:374
-name: Dehydro
-def: "Half of a disulfide bridge." [RESID:AA0025, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=374]
-xref: record_id "374"
-xref: delta_mono_mass "-1.007825"
-xref: delta_avge_mass "-1.0079"
-xref: delta_composition "H(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-06 20:57:01"
-xref: date_time_modified "2006-10-13 18:28:17"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Multiple"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:375
-name: Diphthamide
-def: "Diphthamide." [RESID:AA0040, FindMod:DIPH, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=375]
-xref: record_id "375"
-xref: delta_mono_mass "142.110613"
-xref: delta_avge_mass "142.1989"
-xref: delta_composition "H(14) C(7) N(2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-06 23:21:29"
-xref: date_time_modified "2015-09-08 17:15:11"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:376
-name: Hydroxyfarnesyl
-def: "Hydroxyfarnesyl." [RESID:AA0103, FindMod:FAR0, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=376]
-xref: record_id "376"
-xref: delta_mono_mass "220.182715"
-xref: delta_avge_mass "220.3505"
-xref: delta_composition "H(24) C(15) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-07 20:36:20"
-xref: date_time_modified "2006-10-16 15:20:11"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:377
-name: Diacylglycerol
-def: "Diacylglycerol." [RESID:AA0107, FindMod:DIAC, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=377]
-xref: record_id "377"
-xref: delta_mono_mass "576.511761"
-xref: delta_avge_mass "576.9334"
-xref: delta_composition "H(68) C(37) O(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-07 20:41:21"
-xref: date_time_modified "2006-10-16 17:05:40"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:378
-name: Carboxyethyl
-def: "Carboxyethyl." [RESID:AA0115, FindMod:CETH, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=378]
-synonym: "Ethoxyformylation" RELATED []
-xref: record_id "378"
-xref: delta_mono_mass "72.021129"
-xref: delta_avge_mass "72.0627"
-xref: delta_composition "H(4) C(3) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-07 22:18:20"
-xref: date_time_modified "2024-08-12 10:05:50"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_2_misc_notes "Labeling with diethylpyrocarbonate (DEPC)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:379
-name: Hypusine
-def: "Hypusine." [RESID:AA0116, FindMod:HYPU, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=379]
-xref: record_id "379"
-xref: delta_mono_mass "87.068414"
-xref: delta_avge_mass "87.1204"
-xref: delta_composition "H(9) C(4) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-07 22:20:53"
-xref: date_time_modified "2006-10-16 12:35:24"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:380
-name: Retinylidene
-def: "Retinal." [RESID:AA0120, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=380]
-xref: record_id "380"
-xref: delta_mono_mass "266.203451"
-xref: delta_avge_mass "266.4204"
-xref: delta_composition "H(26) C(20)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-07 22:27:27"
-xref: date_time_modified "2006-10-16 15:47:14"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:381
-name: Lys->AminoadipicAcid
-def: "Alpha-amino adipic acid." [RESID:AA0122, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=381]
-xref: record_id "381"
-xref: delta_mono_mass "14.96328"
-xref: delta_avge_mass "14.9683"
-xref: delta_composition "H(-3) N(-1) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 17:41:37"
-xref: date_time_modified "2006-10-14 10:33:11"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:382
-name: Cys->PyruvicAcid
-def: "Pyruvic acid from N-term cys." [RESID:AA0127, FindMod:PYRUC, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=382]
-xref: record_id "382"
-xref: delta_mono_mass "-33.003705"
-xref: delta_avge_mass "-33.0961"
-xref: delta_composition "H(-3) N(-1) O S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 17:48:42"
-xref: date_time_modified "2006-10-13 16:42:55"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Protein N-term"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:385
-name: Ammonia-loss
-def: "Loss of ammonia." [RESID:AA0127, FindMod:PYRUS, RESID:AA0129, FindMod:OXOB, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=385]
-synonym: "oxobutanoic acid from N term Thr pyruvic acid from N-term ser" RELATED []
-xref: record_id "385"
-xref: delta_mono_mass "-17.026549"
-xref: delta_avge_mass "-17.0305"
-xref: delta_composition "H(-3) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 18:00:01"
-xref: date_time_modified "2007-07-15 20:11:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Protein N-term"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "0"
-xref: spec_3_site "C"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Artefact"
-xref: spec_3_misc_notes "Pyro-carbamidomethyl as a delta from Carbamidomethyl-Cys"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "N"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_4_misc_notes "N-Succinimide"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:387
-name: Phycocyanobilin
-def: "Phycocyanobilin." [RESID:AA0258, RESID:AA0131, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=387]
-comment: Phycocyanobilin and phycobiliviolin have different structures but the same empirical formula.
-synonym: "phycobiliviolin" RELATED []
-xref: record_id "387"
-xref: delta_mono_mass "586.279135"
-xref: delta_avge_mass "586.678"
-xref: delta_composition "H(38) C(33) N(4) O(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 18:06:19"
-xref: date_time_modified "2006-10-16 17:07:44"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:388
-name: Phycoerythrobilin
-def: "Phycoerythrobilin." [RESID:AA0132, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=388]
-xref: record_id "388"
-xref: delta_mono_mass "588.294785"
-xref: delta_avge_mass "588.6939"
-xref: delta_composition "H(40) C(33) N(4) O(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 18:08:38"
-xref: date_time_modified "2006-10-16 17:08:02"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:389
-name: Phytochromobilin
-def: "Phytochromobilin." [RESID:AA0133, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=389]
-xref: record_id "389"
-xref: delta_mono_mass "584.263485"
-xref: delta_avge_mass "584.6621"
-xref: delta_composition "H(36) C(33) N(4) O(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 18:23:58"
-xref: date_time_modified "2006-10-16 17:07:22"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:390
-name: Heme
-def: "Heme." [RESID:AA0329, RESID:AA0135, RESID:AA0276, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=390]
-xref: record_id "390"
-xref: delta_mono_mass "616.177295"
-xref: delta_avge_mass "616.4873"
-xref: delta_composition "H(32) C(34) N(4) O(4) Fe"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 18:27:20"
-xref: date_time_modified "2006-10-16 17:10:28"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:391
-name: Molybdopterin
-def: "Molybdopterin." [RESID:AA0142, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=391]
-xref: record_id "391"
-xref: delta_mono_mass "521.884073"
-xref: delta_avge_mass "520.2668"
-xref: delta_composition "H(11) C(10) N(5) O(8) P S(2) Mo"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 18:46:19"
-xref: date_time_modified "2006-10-16 17:02:25"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:392
-name: Quinone
-def: "Quinone." [RESID:AA0147, RESID:AA0148, FindMod:TOPA, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=392]
-xref: record_id "392"
-xref: delta_mono_mass "29.974179"
-xref: delta_avge_mass "29.9829"
-xref: delta_composition "H(-2) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 18:56:28"
-xref: date_time_modified "2006-10-15 18:03:47"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "W"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:393
-name: Glucosylgalactosyl
-def: "Glucosylgalactosyl hydroxylysine." [RESID:AA0153, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=393]
-xref: record_id "393"
-xref: delta_mono_mass "340.100562"
-xref: delta_avge_mass "340.2806"
-xref: delta_composition "O Hex(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 19:19:13"
-xref: date_time_modified "2015-05-01 14:08:37"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other glycosylation"
-xref: spec_1_neutral_loss_341_mono_mass "340.100562"
-xref: spec_1_neutral_loss_341_avge_mass "340.2806"
-xref: spec_1_neutral_loss_341_flag "false"
-xref: spec_1_neutral_loss_341_composition "O Hex(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:394
-name: GPIanchor
-def: "Glycosylphosphatidylinositol." [RESID:AA0158, RESID:AA0159, RESID:AA0160, RESID:AA0161, RESID:AA0162, RESID:AA0163, RESID:AA0164, RESID:AA0165, RESID:AA0166, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=394]
-xref: record_id "394"
-xref: delta_mono_mass "123.00853"
-xref: delta_avge_mass "123.0477"
-xref: delta_composition "H(6) C(2) N O(3) P"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 19:31:10"
-xref: date_time_modified "2006-11-14 11:13:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Protein C-term"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:395
-name: PhosphoribosyldephosphoCoA
-def: "Phosphoribosyl dephospho-coenzyme A." [RESID:AA0167, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=395]
-xref: record_id "395"
-xref: delta_mono_mass "881.146904"
-xref: delta_avge_mass "881.6335"
-xref: delta_composition "H(42) C(26) N(7) O(19) P(3) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 19:42:56"
-xref: date_time_modified "2006-10-16 17:19:42"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:396
-name: GlycerylPE
-def: "Glycerylphosphorylethanolamine." [RESID:AA0170, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=396]
-xref: record_id "396"
-xref: delta_mono_mass "197.04531"
-xref: delta_avge_mass "197.1262"
-xref: delta_composition "H(12) C(5) N O(5) P"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 19:50:17"
-xref: date_time_modified "2006-10-16 15:08:39"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:397
-name: Triiodothyronine
-def: "Triiodo." [RESID:AA0177, FindMod:THRN, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=397]
-xref: record_id "397"
-xref: delta_mono_mass "469.716159"
-xref: delta_avge_mass "469.785"
-xref: delta_composition "H C(6) O I(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 20:08:28"
-xref: date_time_modified "2006-10-16 16:59:19"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:398
-name: Thyroxine
-def: "Tetraiodo." [RESID:AA0178, FindMod:THRX, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=398]
-xref: record_id "398"
-xref: delta_mono_mass "595.612807"
-xref: delta_avge_mass "595.6815"
-xref: delta_composition "C(6) O I(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 20:10:14"
-xref: date_time_modified "2006-10-16 17:08:51"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:400
-name: Tyr->Dha
-def: "Dehydroalanine (from Tyrosine)." [RESID:AA0181, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=400]
-xref: record_id "400"
-xref: delta_mono_mass "-94.041865"
-xref: delta_avge_mass "-94.1112"
-xref: delta_composition "H(-6) C(-6) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 20:17:48"
-xref: date_time_modified "2006-10-13 15:02:50"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:401
-name: Didehydro
-def: "2-amino-3-oxo-butanoic_acid." [RESID:AA0183, RESID:AA0185, PMID:9252331, RESID:AA0365, FindMod:OXOAS, FindMod:DHY, PMID:15705169, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=401]
-synonym: "oxoalanine" RELATED []
-xref: record_id "401"
-xref: delta_mono_mass "-2.01565"
-xref: delta_avge_mass "-2.0159"
-xref: delta_composition "H(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 20:23:58"
-xref: date_time_modified "2008-07-30 12:01:47"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_2_misc_notes "oxoalanine formylglycine"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "K"
-xref: spec_4_position "Any C-term"
-xref: spec_4_classification "Artefact"
-xref: spec_4_misc_notes "Lactone formation from C-terminal hydroxylysine"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:402
-name: Cys->Oxoalanine
-def: "Oxoalanine." [RESID:AA0185, FindMod:OXOAC, PMID:18722427, PMID:17450134, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=402]
-synonym: "formylglycine" RELATED []
-xref: record_id "402"
-xref: delta_mono_mass "-17.992806"
-xref: delta_avge_mass "-18.0815"
-xref: delta_composition "H(-2) O S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 20:29:10"
-xref: date_time_modified "2009-03-13 16:04:03"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:403
-name: Ser->LacticAcid
-def: "Lactic acid from N-term Ser." [RESID:AA0186, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=403]
-xref: record_id "403"
-xref: delta_mono_mass "-15.010899"
-xref: delta_avge_mass "-15.0146"
-xref: delta_composition "H(-1) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 20:34:16"
-xref: date_time_modified "2006-10-13 17:18:52"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Protein N-term"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:405
-name: Phosphoadenosine
-def: "AMP." [RESID:AA0267, RESID:AA0203, RESID:AA0371, RESID:AA0227, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=405]
-xref: record_id "405"
-xref: delta_mono_mass "329.05252"
-xref: delta_avge_mass "329.2059"
-xref: delta_composition "H(12) C(10) N(5) O(6) P"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 21:34:01"
-xref: date_time_modified "2024-08-12 10:05:28"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_136_mono_mass "135.054495"
-xref: spec_1_neutral_loss_136_avge_mass "135.1267"
-xref: spec_1_neutral_loss_136_flag "false"
-xref: spec_1_neutral_loss_136_composition "H(5) C(5) N(5)"
-xref: spec_1_neutral_loss_250_mono_mass "249.086189"
-xref: spec_1_neutral_loss_250_avge_mass "249.226"
-xref: spec_1_neutral_loss_250_flag "false"
-xref: spec_1_neutral_loss_250_composition "H(11) C(10) N(5) O(3)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-xref: spec_3_neutral_loss_348_mono_mass "347.063085"
-xref: spec_3_neutral_loss_348_avge_mass "347.2212"
-xref: spec_3_neutral_loss_348_flag "false"
-xref: spec_3_neutral_loss_348_composition "H(14) C(10) N(5) O(7) P"
-xref: spec_3_neutral_loss_0_mono_mass "0"
-xref: spec_3_neutral_loss_0_avge_mass "0"
-xref: spec_3_neutral_loss_0_flag "false"
-xref: spec_3_neutral_loss_0_composition "0"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "H"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Post-translational"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "S"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Post-translational"
-xref: spec_5_neutral_loss_348_mono_mass "347.063085"
-xref: spec_5_neutral_loss_348_avge_mass "347.2212"
-xref: spec_5_neutral_loss_348_flag "false"
-xref: spec_5_neutral_loss_348_composition "H(14) C(10) N(5) O(7) P"
-xref: spec_5_neutral_loss_0_mono_mass "0"
-xref: spec_5_neutral_loss_0_avge_mass "0"
-xref: spec_5_neutral_loss_0_flag "false"
-xref: spec_5_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:407
-name: Hydroxycinnamyl
-def: "Hydroxycinnamyl." [RESID:AA0207, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=407]
-xref: record_id "407"
-xref: delta_mono_mass "146.036779"
-xref: delta_avge_mass "146.1427"
-xref: delta_composition "H(6) C(9) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 21:40:43"
-xref: date_time_modified "2006-10-16 14:02:07"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:408
-name: Glycosyl
-def: "Glycosyl-L-hydroxyproline." [RESID:AA0212, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=408]
-xref: record_id "408"
-xref: delta_mono_mass "148.037173"
-xref: delta_avge_mass "148.114"
-xref: delta_composition "H(-2) C(-1) Hex"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 21:57:16"
-xref: date_time_modified "2015-05-01 13:14:26"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other glycosylation"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:409
-name: FMNH
-def: "Flavin mononucleotide." [RESID:AA0353, RESID:AA0220, RESID:AA0352, FindMod:FMNH, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=409]
-xref: record_id "409"
-xref: delta_mono_mass "454.088965"
-xref: delta_avge_mass "454.3279"
-xref: delta_composition "H(19) C(17) N(4) O(9) P"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 22:09:45"
-xref: date_time_modified "2006-10-16 16:57:46"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:410
-name: Archaeol
-def: "S-diphytanylglycerol diether." [RESID:AA0223, FindMod:ARCH, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=410]
-xref: record_id "410"
-xref: delta_mono_mass "634.662782"
-xref: delta_avge_mass "635.1417"
-xref: delta_composition "H(86) C(43) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 22:15:37"
-xref: date_time_modified "2006-10-16 17:10:59"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:411
-name: Phenylisocyanate
-def: "Phenyl isocyanate." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=411]
-xref: record_id "411"
-xref: delta_mono_mass "119.037114"
-xref: delta_avge_mass "119.1207"
-xref: delta_composition "H(5) C(7) N O"
-xref: username_of_poster "TING"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-10-14 21:13:16"
-xref: date_time_modified "2006-10-16 12:48:08"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:412
-name: Phenylisocyanate:2H(5)
-def: "D5-phenyl isocyanate." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=412]
-xref: record_id "412"
-xref: delta_mono_mass "124.068498"
-xref: delta_avge_mass "124.1515"
-xref: delta_composition "2H(5) C(7) N O"
-xref: username_of_poster "TING"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-10-14 21:16:11"
-xref: date_time_modified "2006-10-16 13:35:26"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:413
-name: Phosphoguanosine
-def: "Phospho-guanosine." [RESID:AA0325, RESID:AA0228, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=413]
-xref: record_id "413"
-xref: delta_mono_mass "345.047435"
-xref: delta_avge_mass "345.2053"
-xref: delta_composition "H(12) C(10) N(5) O(7) P"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 15:50:03"
-xref: date_time_modified "2006-10-16 16:01:42"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:414
-name: Hydroxymethyl
-def: "Hydroxymethyl." [RESID:AA0236, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=414]
-xref: record_id "414"
-xref: delta_mono_mass "30.010565"
-xref: delta_avge_mass "30.026"
-xref: delta_composition "H(2) C O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 16:12:56"
-xref: date_time_modified "2006-10-15 18:04:18"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:415
-name: MolybdopterinGD+Delta:S(-1)Se(1)
-def: "L-selenocysteinyl molybdenum bis(molybdopterin guanine dinucleotide)." [RESID:AA0248, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=415]
-xref: record_id "415"
-xref: delta_mono_mass "1620.930224"
-xref: delta_avge_mass "1618.9096"
-xref: delta_composition "H(47) C(40) N(20) O(26) P(4) S(3) Se Mo"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 16:27:56"
-xref: date_time_modified "2006-10-17 11:44:58"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:416
-name: Dipyrrolylmethanemethyl
-def: "Dipyrrolylmethanemethyl." [RESID:AA0252, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=416]
-xref: record_id "416"
-xref: delta_mono_mass "418.137616"
-xref: delta_avge_mass "418.3973"
-xref: delta_composition "H(22) C(20) N(2) O(8)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 16:33:24"
-xref: date_time_modified "2006-11-14 10:37:01"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:417
-name: PhosphoUridine
-def: "Uridine phosphodiester." [RESID:AA0256, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=417]
-xref: record_id "417"
-xref: delta_mono_mass "306.025302"
-xref: delta_avge_mass "306.166"
-xref: delta_composition "H(11) C(9) N(2) O(8) P"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 16:38:18"
-xref: date_time_modified "2006-10-16 15:52:11"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:419
-name: Glycerophospho
-def: "Glycerophospho." [RESID:AA0264, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=419]
-xref: record_id "419"
-xref: delta_mono_mass "154.00311"
-xref: delta_avge_mass "154.0584"
-xref: delta_composition "H(7) C(3) O(5) P"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 17:02:51"
-xref: date_time_modified "2006-10-16 14:03:40"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:420
-name: Carboxy->Thiocarboxy
-def: "Thiocarboxylic acid." [FindMod:THIOG, RESID:AA0265, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=420]
-xref: record_id "420"
-xref: delta_mono_mass "15.977156"
-xref: delta_avge_mass "16.0656"
-xref: delta_composition "O(-1) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 17:08:53"
-xref: date_time_modified "2006-10-14 10:59:20"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Protein C-term"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:421
-name: Sulfide
-def: "Persulfide." [RESID:AA0269, URL:http\://www.nestgrp.com/protocols/bmt/pi3tr.shtml, FindMod:CYSP, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=421]
-xref: record_id "421"
-xref: delta_mono_mass "31.972071"
-xref: delta_avge_mass "32.065"
-xref: delta_composition "S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 17:22:45"
-xref: date_time_modified "2012-11-23 11:25:27"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "D"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_2_misc_notes "beta-thiolation"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "W"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_misc_notes "Addition of a single sulfur atom by Pi3-Tryptophan reagent to create thiol"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:422
-name: PyruvicAcidIminyl
-def: "N-pyruvic acid 2-iminyl." [RESID:AA0287, RESID:AA0274, RESID:AA0275, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=422]
-xref: record_id "422"
-xref: delta_mono_mass "70.005479"
-xref: delta_avge_mass "70.0468"
-xref: delta_composition "H(2) C(3) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 17:30:48"
-xref: date_time_modified "2006-10-16 10:35:08"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Protein N-term"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "V"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:423
-name: Delta:Se(1)
-def: "Selenyl." [RESID:AA0277, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=423]
-xref: record_id "423"
-xref: delta_mono_mass "79.91652"
-xref: delta_avge_mass "78.96"
-xref: delta_composition "Se"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 17:49:48"
-xref: date_time_modified "2006-10-16 11:14:44"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:424
-name: MolybdopterinGD
-def: "Molybdenum bis(molybdopterin guanine dinucleotide)." [RESID:AA0375, RESID:AA0281, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=424]
-xref: record_id "424"
-xref: delta_mono_mass "1572.985775"
-xref: delta_avge_mass "1572.0146"
-xref: delta_composition "H(47) C(40) N(20) O(26) P(4) S(4) Mo"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 17:53:48"
-xref: date_time_modified "2016-02-01 14:23:12"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "D"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "U"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:425
-name: Dioxidation
-def: "Dihydroxy." [PMID:9252331, RESID:AA0282, RESID:AA0370, FindMod:DIHYDR, FindMod:MSONE, FindMod:CSIA, PMID:12686488, RESID:AA0262, RESID:AA0369, RESID:AA0263, RESID:AA0251, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=425]
-xref: record_id "425"
-xref: delta_mono_mass "31.989829"
-xref: delta_avge_mass "31.9988"
-xref: delta_composition "O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 17:59:33"
-xref: date_time_modified "2017-11-03 09:33:41"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "R"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-xref: spec_4_group "4"
-xref: spec_4_hidden "0"
-xref: spec_4_site "M"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Post-translational"
-xref: spec_4_misc_notes "Sulphone"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "F"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_5_misc_notes "phenylalanine oxidation to dihydroxyphenylalanine"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "W"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-xref: spec_6_misc_notes "tryptophan oxidation to formylkynurenin"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "Y"
-xref: spec_7_position "Anywhere"
-xref: spec_7_classification "Post-translational"
-xref: spec_7_misc_notes "trihydroxyphenylalanine"
-xref: spec_8_group "8"
-xref: spec_8_hidden "1"
-xref: spec_8_site "C"
-xref: spec_8_position "Anywhere"
-xref: spec_8_classification "Post-translational"
-xref: spec_8_misc_notes "sulfinic acid"
-xref: spec_9_group "9"
-xref: spec_9_hidden "1"
-xref: spec_9_site "U"
-xref: spec_9_position "Anywhere"
-xref: spec_9_classification "Multiple"
-xref: spec_10_group "10"
-xref: spec_10_hidden "1"
-xref: spec_10_site "E"
-xref: spec_10_position "Anywhere"
-xref: spec_10_classification "Chemical derivative"
-xref: spec_11_group "11"
-xref: spec_11_hidden "1"
-xref: spec_11_site "I"
-xref: spec_11_position "Anywhere"
-xref: spec_11_classification "Chemical derivative"
-xref: spec_12_group "12"
-xref: spec_12_hidden "1"
-xref: spec_12_site "L"
-xref: spec_12_position "Anywhere"
-xref: spec_12_classification "Chemical derivative"
-xref: spec_13_group "13"
-xref: spec_13_hidden "1"
-xref: spec_13_site "V"
-xref: spec_13_position "Anywhere"
-xref: spec_13_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:426
-name: Octanoyl
-def: "Octanoyl." [RESID:AA0290, RESID:AA0386, FindMod:OCTA, RESID:AA0584, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=426]
-xref: record_id "426"
-xref: delta_mono_mass "126.104465"
-xref: delta_avge_mass "126.1962"
-xref: delta_composition "H(14) C(8) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 18:04:46"
-xref: date_time_modified "2013-03-07 10:09:12"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "C"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:428
-name: PhosphoHexNAc
-def: "N-acetylglucosamine-1-phosphoryl." [RESID:AA0296, URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=428]
-xref: record_id "428"
-xref: delta_mono_mass "283.045704"
-xref: delta_avge_mass "283.1724"
-xref: delta_composition "H O(3) P HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 18:15:16"
-xref: date_time_modified "2015-05-01 15:11:15"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_284_mono_mass "283.045704"
-xref: spec_1_neutral_loss_284_avge_mass "283.1724"
-xref: spec_1_neutral_loss_284_flag "false"
-xref: spec_1_neutral_loss_284_composition "H O(3) P HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_284_mono_mass "283.045704"
-xref: spec_1_neutral_loss_284_avge_mass "283.1724"
-xref: spec_1_neutral_loss_284_flag "false"
-xref: spec_1_neutral_loss_284_composition "H O(3) P HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:429
-name: PhosphoHex
-def: "Phosphoglycosyl-D-mannose-1-phosphoryl." [RESID:AA0297, URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=1&hex=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=429]
-xref: record_id "429"
-xref: delta_mono_mass "242.019154"
-xref: delta_avge_mass "242.1205"
-xref: delta_composition "H O(3) P Hex"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 18:18:51"
-xref: date_time_modified "2015-05-01 15:09:57"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_243_mono_mass "242.019154"
-xref: spec_1_neutral_loss_243_avge_mass "242.1205"
-xref: spec_1_neutral_loss_243_flag "false"
-xref: spec_1_neutral_loss_243_composition "H O(3) P Hex"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_243_mono_mass "242.019154"
-xref: spec_1_neutral_loss_243_avge_mass "242.1205"
-xref: spec_1_neutral_loss_243_flag "false"
-xref: spec_1_neutral_loss_243_composition "H O(3) P Hex"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:431
-name: Palmitoleyl
-def: "Palmitoleyl." [RESID:AA0308, FindMod:PALE, PMID:17141155, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=431]
-xref: record_id "431"
-xref: delta_mono_mass "236.214016"
-xref: delta_avge_mass "236.3929"
-xref: delta_composition "H(28) C(16) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 19:57:30"
-xref: date_time_modified "2009-06-21 21:18:50"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Pre-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:432
-name: Cholesterol
-def: "Cholesterol ester." [RESID:AA0309, FindMod:CHOL, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=432]
-xref: record_id "432"
-xref: delta_mono_mass "368.344302"
-xref: delta_avge_mass "368.6383"
-xref: delta_composition "H(44) C(27)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 20:00:10"
-xref: date_time_modified "2006-10-16 16:36:21"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Protein C-term"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:433
-name: Didehydroretinylidene
-def: "3,4-didehydroretinylidene." [RESID:AA0312, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=433]
-xref: record_id "433"
-xref: delta_mono_mass "264.187801"
-xref: delta_avge_mass "264.4046"
-xref: delta_composition "H(24) C(20)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 20:05:19"
-xref: date_time_modified "2006-10-16 15:46:50"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:434
-name: CHDH
-def: "Cis-14-hydroxy-10,13-dioxo-7-heptadecenoic ester." [RESID:AA0316, FindMod:CHDH, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=434]
-xref: record_id "434"
-xref: delta_mono_mass "294.183109"
-xref: delta_avge_mass "294.3859"
-xref: delta_composition "H(26) C(17) O(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 20:08:49"
-xref: date_time_modified "2006-10-16 15:49:28"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:435
-name: Methylpyrroline
-def: "4-methyl-delta-1-pyrroline-5-carboxyl." [RESID:AA0321, FindMod:PYRK, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=435]
-xref: record_id "435"
-xref: delta_mono_mass "109.052764"
-xref: delta_avge_mass "109.1259"
-xref: delta_composition "H(7) C(6) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 20:21:00"
-xref: date_time_modified "2006-10-16 13:37:33"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:436
-name: Hydroxyheme
-def: "Hydroxyheme." [RESID:AA0324, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=436]
-xref: record_id "436"
-xref: delta_mono_mass "614.161645"
-xref: delta_avge_mass "614.4714"
-xref: delta_composition "H(30) C(34) N(4) O(4) Fe"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 20:29:16"
-xref: date_time_modified "2006-10-16 17:10:10"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:437
-name: MicrocinC7
-def: "(3-aminopropyl)(L-aspartyl-1-amino)phosphoryl-5-adenosine." [RESID:AA0328, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=437]
-xref: record_id "437"
-xref: delta_mono_mass "386.110369"
-xref: delta_avge_mass "386.3003"
-xref: delta_composition "H(19) C(13) N(6) O(6) P"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 20:36:37"
-xref: date_time_modified "2006-10-16 16:40:21"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Protein C-term"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:438
-name: Cyano
-def: "Cyano." [RESID:AA0333, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=438]
-xref: record_id "438"
-xref: delta_mono_mass "24.995249"
-xref: delta_avge_mass "25.0095"
-xref: delta_composition "H(-1) C N"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 20:42:40"
-xref: date_time_modified "2006-10-14 19:43:48"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:439
-name: Diironsubcluster
-def: "Hydrogenase diiron subcluster." [RESID:AA0334, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=439]
-xref: record_id "439"
-xref: delta_mono_mass "342.786916"
-xref: delta_avge_mass "342.876"
-xref: delta_composition "H(-1) C(5) N(2) O(5) S(2) Fe(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 20:46:03"
-xref: date_time_modified "2006-10-16 16:01:22"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:440
-name: Amidino
-def: "Amidino." [RESID:AA0335, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=440]
-xref: record_id "440"
-xref: delta_mono_mass "42.021798"
-xref: delta_avge_mass "42.04"
-xref: delta_composition "H(2) C N(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 20:49:10"
-xref: date_time_modified "2006-10-15 19:58:03"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:442
-name: FMN
-def: "O3-(riboflavin phosphoryl)." [RESID:AA0350, RESID:AA0349, FindMod:FMN, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=442]
-xref: record_id "442"
-xref: delta_mono_mass "438.094051"
-xref: delta_avge_mass "438.3285"
-xref: delta_composition "H(19) C(17) N(4) O(8) P"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 21:11:32"
-xref: date_time_modified "2006-10-16 16:47:27"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:443
-name: FMNC
-def: "S-(4a-FMN)." [RESID:AA0351, FindMod:FMNC, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=443]
-xref: record_id "443"
-xref: delta_mono_mass "456.104615"
-xref: delta_avge_mass "456.3438"
-xref: delta_composition "H(21) C(17) N(4) O(9) P"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 21:21:47"
-xref: date_time_modified "2006-10-16 16:58:10"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:444
-name: CuSMo
-def: "Copper sulfido molybdopterin cytosine dinuncleotide." [RESID:AA0355, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=444]
-xref: record_id "444"
-xref: delta_mono_mass "922.834855"
-xref: delta_avge_mass "922.067"
-xref: delta_composition "H(24) C(19) N(8) O(15) P(2) S(3) Cu Mo"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 21:34:38"
-xref: date_time_modified "2006-10-16 17:20:14"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:445
-name: Hydroxytrimethyl
-def: "5-hydroxy-N6,N6,N6-trimethyl." [RESID:AA0359, FindMod:TRIMETK, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=445]
-xref: record_id "445"
-xref: delta_mono_mass "59.04969"
-xref: delta_avge_mass "59.0871"
-xref: delta_composition "H(7) C(3) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 21:40:08"
-xref: date_time_modified "2006-10-16 10:28:02"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:447
-name: Deoxy
-def: "Reduction." [RESID:AA0191, PMID:14235557, RESID:AA0373, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=447]
-synonym: "Serine to Alanine Threonine to a-aminobutyrate" RELATED []
-xref: record_id "447"
-xref: delta_mono_mass "-15.994915"
-xref: delta_avge_mass "-15.9994"
-xref: delta_composition "O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 22:00:35"
-xref: date_time_modified "2006-10-13 17:16:30"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_2_misc_notes "Beta elimination of O-glycosylation under alkaline conditions followed by reduction"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_misc_notes "Beta elimination of O-glycosylation under alkaline conditions followed by reduction"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:448
-name: Microcin
-def: "Microcin E492 siderophore ester from serine." [RESID:AA0374, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=448]
-xref: record_id "448"
-xref: delta_mono_mass "831.197041"
-xref: delta_avge_mass "831.6871"
-xref: delta_composition "H(37) C(36) N(3) O(20)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 22:04:46"
-xref: date_time_modified "2006-10-16 17:18:24"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Protein C-term"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:449
-name: Decanoyl
-def: "Lipid." [RESID:AA0387, RESID:AA0385, FindMod:DECA, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=449]
-xref: record_id "449"
-xref: delta_mono_mass "154.135765"
-xref: delta_avge_mass "154.2493"
-xref: delta_composition "H(18) C(10) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 22:14:11"
-xref: date_time_modified "2006-10-16 14:04:24"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:450
-name: Glu
-def: "Monoglutamyl." [PMID:12356754, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=450]
-xref: record_id "450"
-xref: delta_mono_mass "129.042593"
-xref: delta_avge_mass "129.114"
-xref: delta_composition "H(7) C(5) N O(3)"
-xref: username_of_poster "vcavett"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-10-18 15:07:18"
-xref: date_time_modified "2006-10-17 13:48:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Protein C-term"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "E"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:451
-name: GluGlu
-def: "Diglutamyl." [PMID:12356754, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=451]
-xref: record_id "451"
-xref: delta_mono_mass "258.085186"
-xref: delta_avge_mass "258.228"
-xref: delta_composition "H(14) C(10) N(2) O(6)"
-xref: username_of_poster "vcavett"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-10-18 15:17:59"
-xref: date_time_modified "2006-10-17 13:49:07"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Protein C-term"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "E"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:452
-name: GluGluGlu
-def: "Triglutamyl." [PMID:12356754, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=452]
-xref: record_id "452"
-xref: delta_mono_mass "387.127779"
-xref: delta_avge_mass "387.3419"
-xref: delta_composition "H(21) C(15) N(3) O(9)"
-xref: username_of_poster "vcavett"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-10-18 15:21:01"
-xref: date_time_modified "2006-10-17 14:11:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Protein C-term"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "E"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:453
-name: GluGluGluGlu
-def: "Tetraglutamyl." [PMID:12356754, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=453]
-xref: record_id "453"
-xref: delta_mono_mass "516.170373"
-xref: delta_avge_mass "516.4559"
-xref: delta_composition "H(28) C(20) N(4) O(12)"
-xref: username_of_poster "vcavett"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-10-18 15:22:24"
-xref: date_time_modified "2006-10-17 14:16:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Protein C-term"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "E"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:454
-name: HexN
-def: "Hexosamine." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hexn=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=454]
-synonym: "Glucosamine Galactosamine" RELATED []
-xref: record_id "454"
-xref: delta_mono_mass "161.068808"
-xref: delta_avge_mass "161.1558"
-xref: delta_composition "HexN"
-xref: username_of_poster "xyuan"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-11-08 18:58:20"
-xref: date_time_modified "2015-05-01 16:57:37"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Synth. pep. protect. gp."
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_162_mono_mass "161.068808"
-xref: spec_2_neutral_loss_162_avge_mass "161.1558"
-xref: spec_2_neutral_loss_162_flag "false"
-xref: spec_2_neutral_loss_162_composition "HexN"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "O-linked glycosylation"
-xref: spec_3_neutral_loss_0_mono_mass "0"
-xref: spec_3_neutral_loss_0_avge_mass "0"
-xref: spec_3_neutral_loss_0_flag "false"
-xref: spec_3_neutral_loss_0_composition "0"
-xref: spec_3_neutral_loss_162_mono_mass "161.068808"
-xref: spec_3_neutral_loss_162_avge_mass "161.1558"
-xref: spec_3_neutral_loss_162_flag "false"
-xref: spec_3_neutral_loss_162_composition "HexN"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "S"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "O-linked glycosylation"
-xref: spec_3_neutral_loss_0_mono_mass "0"
-xref: spec_3_neutral_loss_0_avge_mass "0"
-xref: spec_3_neutral_loss_0_flag "false"
-xref: spec_3_neutral_loss_0_composition "0"
-xref: spec_3_neutral_loss_162_mono_mass "161.068808"
-xref: spec_3_neutral_loss_162_avge_mass "161.1558"
-xref: spec_3_neutral_loss_162_flag "false"
-xref: spec_3_neutral_loss_162_composition "HexN"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "W"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Other glycosylation"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:455
-name: Xlink:DMP[154]
-def: "Free monolink of DMP crosslinker." [URL:http\://tools.thermofisher.com/content/sfs/manuals/MAN0011314_ImidoesterCrsLnk_DMA_DMP_DMS_DTBP_UG.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=455]
-synonym: "Dimethyl pimelimidate" RELATED []
-xref: record_id "455"
-xref: delta_mono_mass "154.110613"
-xref: delta_avge_mass "154.2096"
-xref: delta_composition "H(14) C(8) N(2) O"
-xref: username_of_poster "mariana"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-11-08 20:09:24"
-xref: date_time_modified "2017-08-18 10:27:36"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:457
-name: NDA
-def: "Naphthalene-2,3-dicarboxaldehyde." [PMID:2081203, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=457]
-comment: Fluorescent derivative.
-xref: record_id "457"
-xref: delta_mono_mass "175.042199"
-xref: delta_avge_mass "175.1855"
-xref: delta_composition "H(5) C(13) N"
-xref: username_of_poster "Dekker"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-11-11 11:03:32"
-xref: date_time_modified "2006-10-17 13:41:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:464
-name: SPITC:13C(6)
-def: "4-sulfophenyl isothiocyanate (Heavy C13)." [PMID:16526082, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=464]
-synonym: "N-terminal / lysine sulfonation" RELATED []
-xref: record_id "464"
-xref: delta_mono_mass "220.991213"
-xref: delta_avge_mass "221.2054"
-xref: delta_composition "H(5) C 13C(6) N O(3) S(2)"
-xref: username_of_poster "apanchaud"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-12-19 08:37:57"
-xref: date_time_modified "2006-10-16 15:25:36"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:472
-name: AEC-MAEC
-def: "Aminoethylcysteine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=472]
-comment: Modification procedure used for phosphopeptide mapping.
-synonym: "beta-methylaminoethylcysteine" RELATED []
-xref: record_id "472"
-xref: delta_mono_mass "59.019355"
-xref: delta_avge_mass "59.1334"
-xref: delta_composition "H(5) C(2) N O(-1) S"
-xref: username_of_poster "mpcusack"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-01-20 00:46:08"
-xref: date_time_modified "2007-09-26 22:43:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "pS gives aminoethylcysteine"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_2_misc_notes "pT gives beta-methylaminoethylcysteine"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:476
-name: TMAB
-def: "4-trimethyllammoniumbutyryl-." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=476]
-xref: record_id "476"
-xref: delta_mono_mass "128.107539"
-xref: delta_avge_mass "128.1922"
-xref: delta_composition "H(14) C(7) N O"
-xref: username_of_poster "xwei"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-02-15 03:10:16"
-xref: date_time_modified "2006-10-17 12:08:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_neutral_loss_60_mono_mass "59.073499"
-xref: spec_1_neutral_loss_60_avge_mass "59.1103"
-xref: spec_1_neutral_loss_60_flag "false"
-xref: spec_1_neutral_loss_60_composition "H(9) C(3) N"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_2_neutral_loss_60_mono_mass "59.073499"
-xref: spec_2_neutral_loss_60_avge_mass "59.1103"
-xref: spec_2_neutral_loss_60_flag "false"
-xref: spec_2_neutral_loss_60_composition "H(9) C(3) N"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:477
-name: TMAB:2H(9)
-def: "D9-4-trimethyllammoniumbutyryl-." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=477]
-xref: record_id "477"
-xref: delta_mono_mass "137.16403"
-xref: delta_avge_mass "137.2476"
-xref: delta_composition "H(5) 2H(9) C(7) N O"
-xref: username_of_poster "xwei"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-02-15 18:36:06"
-xref: date_time_modified "2006-10-17 12:08:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_neutral_loss_69_mono_mass "68.12999"
-xref: spec_1_neutral_loss_69_avge_mass "68.1657"
-xref: spec_1_neutral_loss_69_flag "false"
-xref: spec_1_neutral_loss_69_composition "2H(9) C(3) N"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_2_neutral_loss_69_mono_mass "68.12999"
-xref: spec_2_neutral_loss_69_avge_mass "68.1657"
-xref: spec_2_neutral_loss_69_flag "false"
-xref: spec_2_neutral_loss_69_composition "2H(9) C(3) N"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:478
-name: FTC
-def: "Fluorescein-5-thiosemicarbazide." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=478]
-xref: record_id "478"
-xref: delta_mono_mass "421.073241"
-xref: delta_avge_mass "421.4259"
-xref: delta_composition "H(15) C(21) N(3) O(5) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2006-02-20 11:15:03"
-xref: date_time_modified "2006-10-16 16:45:27"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "P"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "R"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "S"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:481
-name: Label:2H(4)
-def: "4,4,5,5-D4 Lysine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=481]
-comment: For SILAC experiments.
-synonym: "Alanine-2,3,3,3-d4" RELATED []
-xref: record_id "481"
-xref: delta_mono_mass "4.025107"
-xref: delta_avge_mass "4.0246"
-xref: delta_composition "H(-4) 2H(4)"
-xref: username_of_poster "yunwah"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-02-20 11:44:19"
-xref: date_time_modified "2019-01-10 15:45:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "F"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Cambridge Labs DLM-451"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "A"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "485845 Aldrich"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "U"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:488
-name: DHP
-def: "Dehydropyrrolizidine alkaloid (dehydroretronecine) on cysteines." [PMID:16222722, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=488]
-synonym: "Dehydroretronecine" RELATED []
-xref: record_id "488"
-xref: delta_mono_mass "118.065674"
-xref: delta_avge_mass "118.1558"
-xref: delta_composition "H(8) C(8) N"
-xref: username_of_poster "rowanrainbow"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-03-07 08:40:13"
-xref: date_time_modified "2006-10-17 12:07:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:490
-name: Hep
-def: "Heptose." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=490]
-xref: record_id "490"
-xref: delta_mono_mass "192.063388"
-xref: delta_avge_mass "192.1666"
-xref: delta_composition "Hep"
-xref: username_of_poster "anikolakakis"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-03-24 15:59:43"
-xref: date_time_modified "2015-05-05 15:58:34"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other glycosylation"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_193_mono_mass "192.063388"
-xref: spec_2_neutral_loss_193_avge_mass "192.1666"
-xref: spec_2_neutral_loss_193_flag "false"
-xref: spec_2_neutral_loss_193_composition "Hep"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Q"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Other glycosylation"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "R"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "N-linked glycosylation"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "T"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "O-linked glycosylation"
-xref: spec_5_neutral_loss_193_mono_mass "192.063388"
-xref: spec_5_neutral_loss_193_avge_mass "192.1666"
-xref: spec_5_neutral_loss_193_flag "false"
-xref: spec_5_neutral_loss_193_composition "Hep"
-xref: spec_5_neutral_loss_0_mono_mass "0"
-xref: spec_5_neutral_loss_0_avge_mass "0"
-xref: spec_5_neutral_loss_0_flag "false"
-xref: spec_5_neutral_loss_0_composition "0"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "S"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "O-linked glycosylation"
-xref: spec_5_neutral_loss_193_mono_mass "192.063388"
-xref: spec_5_neutral_loss_193_avge_mass "192.1666"
-xref: spec_5_neutral_loss_193_flag "false"
-xref: spec_5_neutral_loss_193_composition "Hep"
-xref: spec_5_neutral_loss_0_mono_mass "0"
-xref: spec_5_neutral_loss_0_avge_mass "0"
-xref: spec_5_neutral_loss_0_flag "false"
-xref: spec_5_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:493
-name: BADGE
-def: "Bisphenol A diglycidyl ether derivative." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=493]
-comment: Found in canned food products.
-xref: record_id "493"
-xref: delta_mono_mass "340.167459"
-xref: delta_avge_mass "340.4129"
-xref: delta_composition "H(24) C(21) O(4)"
-xref: username_of_poster "TNO"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-03-27 09:30:54"
-xref: date_time_modified "2006-10-17 14:09:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Non-standard residue"
-xref: spec_1_misc_notes "found in canned food products"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:494
-name: CyDye-Cy3
-def: "Cy3 CyDye DIGE Fluor saturation dye." [PMID:12872219, URL:https\://www.gelifesciences.com/gehcls_images/GELS/Related%20Content/Files/1314735988470/litdoc28953107AD_20110831002141.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=494]
-synonym: "Formula needs confirmation" RELATED []
-xref: record_id "494"
-xref: delta_mono_mass "672.298156"
-xref: delta_avge_mass "672.8335"
-xref: delta_composition "H(44) C(37) N(4) O(6) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2006-03-27 11:17:51"
-xref: date_time_modified "2012-09-15 00:20:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:495
-name: CyDye-Cy5
-def: "Cy5 CyDye DIGE Fluor saturation dye." [PMID:12872219, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=495]
-xref: record_id "495"
-xref: delta_mono_mass "684.298156"
-xref: delta_avge_mass "684.8442"
-xref: delta_composition "H(44) C(38) N(4) O(6) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2006-03-27 11:53:04"
-xref: date_time_modified "2006-10-17 14:18:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:498
-name: BHTOH
-def: "Michael addition of t-butyl hydroxylated BHT (BHTOH) to C, H or K." [PMID:16533022, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=498]
-comment: BHTOH is formed upon metabolism of BHT with P450 enzymes. The BHTOH is further metabolized to its quinone methide (electrophile) which reacts with -SH and -NH2 groups.
-synonym: "t-butyl hydroxylated BHT" RELATED []
-xref: record_id "498"
-xref: delta_mono_mass "234.16198"
-xref: delta_avge_mass "234.334"
-xref: delta_composition "H(22) C(15) O(2)"
-xref: username_of_poster "rkupfer"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-04-10 19:27:51"
-xref: date_time_modified "2006-10-17 13:42:22"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_1_misc_notes "primary adduct"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Other"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:499
-name: IGBP:13C(2)
-def: "Heavy IDBEST tag for quantitation." [URL:http\://www.targetdiscovery.com/index.php?topic=prod.idbe, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=499]
-xref: record_id "499"
-xref: delta_mono_mass "298.022748"
-xref: delta_avge_mass "299.1331"
-xref: delta_composition "H(13) C(10) 13C(2) N(2) O(2) Br"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2006-04-14 18:44:41"
-xref: date_time_modified "2006-10-19 10:48:25"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:500
-name: Nmethylmaleimide+water
-def: "Nmethylmaleimidehydrolysis." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=500]
-xref: record_id "500"
-xref: delta_mono_mass "129.042593"
-xref: delta_avge_mass "129.114"
-xref: delta_composition "H(7) C(5) N O(3)"
-xref: username_of_poster "whaskins"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-04-14 22:58:34"
-xref: date_time_modified "2006-10-17 12:12:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:501
-name: PyMIC
-def: "3-methyl-2-pyridyl isocyanate." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=501]
-xref: record_id "501"
-xref: delta_mono_mass "134.048013"
-xref: delta_avge_mass "134.1353"
-xref: delta_composition "H(6) C(7) N(2) O"
-xref: username_of_poster "TING"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-04-18 20:46:17"
-xref: date_time_modified "2006-10-17 12:19:15"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:503
-name: LG-lactam-K
-def: "Levuglandinyl - lysine lactam adduct." [PMID:15650407, PMID:15752459, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=503]
-xref: record_id "503"
-xref: delta_mono_mass "332.19876"
-xref: delta_avge_mass "332.4339"
-xref: delta_composition "H(28) C(20) O(4)"
-xref: username_of_poster "alexparf"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-04-27 17:56:39"
-xref: date_time_modified "2006-11-14 12:04:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:504
-name: LG-Hlactam-K
-def: "Levuglandinyl - lysine hydroxylactam adduct." [PMID:15650407, PMID:15752459, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=504]
-xref: record_id "504"
-xref: delta_mono_mass "348.193674"
-xref: delta_avge_mass "348.4333"
-xref: delta_composition "H(28) C(20) O(5)"
-xref: username_of_poster "alexparf"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-04-27 18:02:17"
-xref: date_time_modified "2006-11-14 12:04:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:505
-name: LG-lactam-R
-def: "Levuglandinyl - arginine lactam adduct." [PMID:15650407, PMID:15752459, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=505]
-xref: record_id "505"
-xref: delta_mono_mass "290.176961"
-xref: delta_avge_mass "290.3939"
-xref: delta_composition "H(26) C(19) N(-2) O(4)"
-xref: username_of_poster "alexparf"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-04-27 18:05:11"
-xref: date_time_modified "2006-10-17 14:08:20"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:506
-name: LG-Hlactam-R
-def: "Levuglandinyl - arginine hydroxylactam adduct." [PMID:15650407, PMID:15752459, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=506]
-xref: record_id "506"
-xref: delta_mono_mass "306.171876"
-xref: delta_avge_mass "306.3933"
-xref: delta_composition "H(26) C(19) N(-2) O(5)"
-xref: username_of_poster "alexparf"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-04-27 18:08:11"
-xref: date_time_modified "2006-10-17 14:08:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:510
-name: Dimethyl:2H(4)13C(2)
-def: "DiMethyl-C13HD2." [PMID:16335955, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=510]
-xref: record_id "510"
-xref: delta_mono_mass "34.063117"
-xref: delta_avge_mass "34.0631"
-xref: delta_composition "2H(4) 13C(2)"
-xref: username_of_poster "oded"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-05-08 22:03:41"
-xref: date_time_modified "2014-11-16 07:37:20"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "R"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "N-term"
-xref: spec_4_position "Protein N-term"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "When dimethyl labelling is pre-digest"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:512
-name: Hex(2)
-def: "Lactosylation." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=512]
-comment: Lactosylation of bovine Beta-Lactoglobulin.
-synonym: "lac" RELATED []
-xref: record_id "512"
-xref: delta_mono_mass "324.105647"
-xref: delta_avge_mass "324.2812"
-xref: delta_composition "Hex(2)"
-xref: username_of_poster "molle"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-05-11 13:21:17"
-xref: date_time_modified "2017-11-23 12:59:14"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other glycosylation"
-xref: spec_1_misc_notes "Maillard reaction (first event)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "R"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Other glycosylation"
-xref: spec_2_misc_notes "Maillard reaction (first event)"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "S"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "O-linked glycosylation"
-xref: spec_3_neutral_loss_0_mono_mass "0"
-xref: spec_3_neutral_loss_0_avge_mass "0"
-xref: spec_3_neutral_loss_0_flag "false"
-xref: spec_3_neutral_loss_0_composition "0"
-xref: spec_3_neutral_loss_325_mono_mass "324.105647"
-xref: spec_3_neutral_loss_325_avge_mass "324.2812"
-xref: spec_3_neutral_loss_325_flag "false"
-xref: spec_3_neutral_loss_325_composition "Hex(2)"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "O-linked glycosylation"
-xref: spec_3_neutral_loss_0_mono_mass "0"
-xref: spec_3_neutral_loss_0_avge_mass "0"
-xref: spec_3_neutral_loss_0_flag "false"
-xref: spec_3_neutral_loss_0_composition "0"
-xref: spec_3_neutral_loss_325_mono_mass "324.105647"
-xref: spec_3_neutral_loss_325_avge_mass "324.2812"
-xref: spec_3_neutral_loss_325_flag "false"
-xref: spec_3_neutral_loss_325_composition "Hex(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:513
-name: C8-QAT
-def: "[3-(2,5)-Dioxopyrrolidin-1-yloxycarbonyl)-propyl]dimethyloctylammonium." [PMID:16771548, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=513]
-xref: record_id "513"
-xref: delta_mono_mass "227.224915"
-xref: delta_avge_mass "227.3862"
-xref: delta_composition "H(29) C(14) N O"
-xref: username_of_poster "amadian"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-05-13 20:55:20"
-xref: date_time_modified "2006-12-03 19:43:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:514
-name: PropylNAGthiazoline
-def: "Propyl-1,2-dideoxy-2\'-methyl-alpha-D-glucopyranoso-[2,1-d]-Delta2\'-thiazoline." [PMID:15795231, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=514]
-comment: In a recent publication (see reference), we have shown that family 84 glycoside hydrolases contain a deep pocket beneath the 2-acetamido group of its substrate (N-acetyl-glucosamine). With this strucual feature in mind, we have designed a specific inhibitor that contains a chloride group appended to the end of the propyl chain on a known inhibitor termed propyl-NAG-thiazoline. We have shown kinetically that this molecule is a potent suicide inhibitor of this enzyme famiy and now wish to know the precise residue which is acting as the nucleophile to dispace the choride atom. We have included all residues that are in the vacinity of the chloride atom that could potentially act in a nucleophilic manner.
-xref: record_id "514"
-xref: delta_mono_mass "232.064354"
-xref: delta_avge_mass "232.2768"
-xref: delta_composition "H(14) C(9) N O(4) S"
-xref: username_of_poster "mmacaule"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-05-18 18:44:52"
-xref: date_time_modified "2015-05-01 13:33:58"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:515
-name: FNEM
-def: "Fluorescein-5-maleimide." [PMID:9325338, PMID:11665566, URL:http\://probes.invitrogen.com/media/pis/mp00003.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=515]
-synonym: "fluorescein-NEM" RELATED []
-xref: record_id "515"
-xref: delta_mono_mass "427.069202"
-xref: delta_avge_mass "427.3625"
-xref: delta_composition "H(13) C(24) N O(7)"
-xref: username_of_poster "shure"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-06-08 10:07:56"
-xref: date_time_modified "2006-10-17 14:15:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "photosensitive"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:518
-name: Diethyl
-def: "Diethylation, analogous to Dimethylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=518]
-xref: record_id "518"
-xref: delta_mono_mass "56.0626"
-xref: delta_avge_mass "56.1063"
-xref: delta_composition "H(8) C(4)"
-xref: username_of_poster "PhilipHsu"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-06-15 07:18:26"
-xref: date_time_modified "2006-10-17 12:00:33"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:519
-name: BisANS
-def: "4,4\'-dianilino-1,1\'-binaphthyl-5,5\'-disulfonic acid." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=519]
-xref: record_id "519"
-xref: delta_mono_mass "594.091928"
-xref: delta_avge_mass "594.6569"
-xref: delta_composition "H(22) C(32) N(2) O(6) S(2)"
-xref: username_of_poster "app95d"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-07-05 23:31:08"
-xref: date_time_modified "2012-05-15 20:15:06"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:520
-name: Piperidine
-def: "Piperidination." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=520]
-xref: record_id "520"
-xref: delta_mono_mass "68.0626"
-xref: delta_avge_mass "68.117"
-xref: delta_composition "H(8) C(5)"
-xref: username_of_poster "PhilipHsu"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-07-20 08:37:21"
-xref: date_time_modified "2006-10-17 12:05:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:522
-name: Maleimide-PEO2-Biotin
-def: "Maleimide-Biotin." [URL:http\://www.piercenet.com/Products/Browse.cfm?fldID=01031005, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=522]
-synonym: "Maleimide-PEG2-Biotin" RELATED []
-xref: record_id "522"
-xref: delta_mono_mass "525.225719"
-xref: delta_avge_mass "525.6183"
-xref: delta_composition "H(35) C(23) N(5) O(7) S"
-xref: username_of_poster "ericjohansen"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-08-11 02:49:51"
-xref: date_time_modified "2010-12-03 16:13:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:523
-name: Sulfo-NHS-LC-LC-Biotin
-def: "Biot_LC_LC." [URL:http\://www.piercenet.com/Products/Browse.cfm?fldID=8D38BA83-EFDC-421A-853F-E96EBA380612, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=523]
-synonym: "Sulfo-NHS-LC-LC-Biotin" RELATED []
-xref: record_id "523"
-xref: delta_mono_mass "452.245726"
-xref: delta_avge_mass "452.6106"
-xref: delta_composition "H(36) C(22) N(4) O(4) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2006-08-31 18:01:50"
-xref: date_time_modified "2010-12-03 16:11:08"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:525
-name: CLIP_TRAQ_2
-def: "CLIP_TRAQ_2." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=525]
-comment: CLIP-TRAQ-2 H(17) C(10) C13 N(3) O(4) is an in-house made compound that reacts with primary amines through a N-hydroxysuccinimide group leading to a 141.0983 Da mass shift (monoisotopic) in MS mode. The reporter ion in MS/MS mode can either be 113 or 114 m/z depending on the position of isotopic C13 in the molecule. (Fahlman, R. and Overall, C.M. ; in preparation).
-synonym: "CLIP_TRAQ_double" RELATED []
-xref: record_id "525"
-xref: delta_mono_mass "141.098318"
-xref: delta_avge_mass "141.1756"
-xref: delta_composition "H(12) C(6) 13C N(2) O"
-xref: username_of_poster "overalllab"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-09-15 02:25:46"
-xref: date_time_modified "2006-10-17 18:04:46"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Side reaction, low abundance"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:526
-name: Dethiomethyl
-def: "Prompt loss of side chain from oxidised Met." [PMID:9004526, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=526]
-comment: More commonly seen as a neutral loss.
-xref: record_id "526"
-xref: delta_mono_mass "-48.003371"
-xref: delta_avge_mass "-48.1075"
-xref: delta_composition "H(-4) C(-1) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-10-13 15:14:55"
-xref: date_time_modified "2006-10-13 17:02:27"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:528
-name: Methyl+Deamidated
-def: "Deamidation followed by a methylation." [FindMod:DEAME, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=528]
-synonym: "Glutamate methyl ester" RELATED []
-xref: record_id "528"
-xref: delta_mono_mass "14.999666"
-xref: delta_avge_mass "15.0113"
-xref: delta_composition "H C N(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-10-14 10:39:08"
-xref: date_time_modified "2007-02-04 12:25:42"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:529
-name: Delta:H(5)C(2)
-def: "Dimethylation of proline residue." [FindMod:DIMETP, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=529]
-xref: record_id "529"
-xref: delta_mono_mass "29.039125"
-xref: delta_avge_mass "29.0611"
-xref: delta_composition "H(5) C(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-10-15 18:02:34"
-xref: date_time_modified "2006-10-15 18:03:16"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:530
-name: Cation:K
-def: "Replacement of proton by potassium." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=530]
-xref: record_id "530"
-xref: delta_mono_mass "37.955882"
-xref: delta_avge_mass "38.0904"
-xref: delta_composition "H(-1) K"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-10-15 18:29:43"
-xref: date_time_modified "2006-10-18 11:17:39"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:531
-name: Cation:Cu[I]
-def: "Replacement of proton by copper." [URL:http\://www.uniprot.org/uniprot/P07509, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=531]
-xref: record_id "531"
-xref: delta_mono_mass "61.921774"
-xref: delta_avge_mass "62.5381"
-xref: delta_composition "H(-1) Cu"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-10-16 10:29:12"
-xref: date_time_modified "2015-03-19 09:33:03"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "H"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:532
-name: iTRAQ4plex114
-def: "Accurate mass for 114." [URL:http\://docs.appliedbiosystems.com/pebiodocs/04351918.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=532]
-comment: Different channels have the same nominal mass but slightly different exact masses.
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED []
-xref: record_id "532"
-xref: delta_mono_mass "144.105918"
-xref: delta_avge_mass "144.168"
-xref: delta_composition "H(12) C(5) 13C(2) N(2) 18O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-10-16 13:46:49"
-xref: date_time_modified "2024-08-12 09:55:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Low abundance"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "C"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "side reaction"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:533
-name: iTRAQ4plex115
-def: "Accurate mass for 115." [URL:http\://docs.appliedbiosystems.com/pebiodocs/04351918.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=533]
-comment: Different channels have the same nominal mass but slightly different exact masses.
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED []
-xref: record_id "533"
-xref: delta_mono_mass "144.099599"
-xref: delta_avge_mass "144.1688"
-xref: delta_composition "H(12) C(6) 13C N 15N 18O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-10-16 13:48:16"
-xref: date_time_modified "2024-08-12 09:55:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Low abundance"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "C"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "side reaction"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:534
-name: Dibromo
-def: "Dibromo." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=534]
-xref: record_id "534"
-xref: delta_mono_mass "155.821022"
-xref: delta_avge_mass "157.7921"
-xref: delta_composition "H(-2) Br(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-10-16 14:06:38"
-xref: date_time_modified "2006-10-16 14:06:38"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:535
-name: LRGG
-def: "Ubiquitination." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=535]
-synonym: "Addition of LRGG" RELATED []
-xref: record_id "535"
-xref: delta_mono_mass "383.228103"
-xref: delta_avge_mass "383.446"
-xref: delta_composition "H(29) C(16) N(7) O(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-10-16 16:39:05"
-xref: date_time_modified "2014-07-09 16:48:40"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:536
-name: CLIP_TRAQ_3
-def: "CLIP_TRAQ_3." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=536]
-comment: CLIP_TRAQ_3 (H(20) C(11) C13 N(3) O(4) is an in-house made compound that reacts with primary amines through a N-hydroxysuccinimide group leading to a 155.1 Da mass shift (monoisotopic) in MS mode. The reporter ion in MS/MS mode can either be 127 or 128 m/z depending on the position of isotopic C13 in the molecule. (Fahlman, R. and Overall, C.M. ; in preparation).
-xref: record_id "536"
-xref: delta_mono_mass "271.148736"
-xref: delta_avge_mass "271.2976"
-xref: delta_composition "H(20) C(11) 13C N(3) O(4)"
-xref: username_of_poster "overall"
-xref: group_of_poster ""
-xref: date_time_posted "2006-10-17 18:08:00"
-xref: date_time_modified "2006-10-17 18:11:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Low abundance"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:537
-name: CLIP_TRAQ_4
-def: "CLIP_TRAQ_4." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=537]
-comment: CLIP_TRAQ_4 is an in-house made compound that reacts with primary amines through a N-hydroxysuccinimide group leading to a 128.1 Da mass shift (monoisotopic) in MS mode. The reporter ion in MS/MS mode can either be 100 or 101 m/z depending on the position of isotopic C13 in the molecule. (Fahlman, R. and Overall, C.M. ; in preparation).
-xref: record_id "537"
-xref: delta_mono_mass "244.101452"
-xref: delta_avge_mass "244.2292"
-xref: delta_composition "H(15) C(9) 13C N(2) O(5)"
-xref: username_of_poster "overall"
-xref: group_of_poster ""
-xref: date_time_posted "2006-10-17 18:09:22"
-xref: date_time_modified "2006-10-17 18:10:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Low abundance"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:538
-name: Biotin:Cayman-10141
-def: "Was 15dB-biotin." [URL:http\://www.caymanchem.com/pdfs/10141.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=538]
-synonym: "15-deoxy-delta 12,14-Prostaglandin J2-biotinimide" RELATED []
-xref: record_id "538"
-xref: delta_mono_mass "626.386577"
-xref: delta_avge_mass "626.8927"
-xref: delta_composition "H(54) C(35) N(4) O(4) S"
-xref: username_of_poster "sevgh"
-xref: group_of_poster ""
-xref: date_time_posted "2006-10-17 18:13:45"
-xref: date_time_modified "2010-12-03 16:08:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:539
-name: Biotin:Cayman-10013
-def: "Was PGA1-biotin." [URL:http\://www.caymanchem.com/pdfs/10013.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=539]
-synonym: "Prostaglandin A1-biotinimide" RELATED []
-xref: record_id "539"
-xref: delta_mono_mass "660.428442"
-xref: delta_avge_mass "660.9504"
-xref: delta_composition "H(60) C(36) N(4) O(5) S"
-xref: username_of_poster "sevgh"
-xref: group_of_poster ""
-xref: date_time_posted "2006-10-17 18:24:06"
-xref: date_time_modified "2010-12-03 16:07:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:540
-name: Ala->Ser
-def: "Ala->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=540]
-xref: record_id "540"
-xref: delta_mono_mass "15.994915"
-xref: delta_avge_mass "15.9994"
-xref: delta_composition "O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:07:30"
-xref: date_time_modified "2006-11-09 10:07:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:541
-name: Ala->Thr
-def: "Ala->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=541]
-xref: record_id "541"
-xref: delta_mono_mass "30.010565"
-xref: delta_avge_mass "30.026"
-xref: delta_composition "H(2) C O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:13:43"
-xref: date_time_modified "2006-11-09 10:13:43"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:542
-name: Ala->Asp
-def: "Ala->Asp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=542]
-xref: record_id "542"
-xref: delta_mono_mass "43.989829"
-xref: delta_avge_mass "44.0095"
-xref: delta_composition "C O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:15:05"
-xref: date_time_modified "2006-11-09 10:15:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:543
-name: Ala->Pro
-def: "Ala->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=543]
-xref: record_id "543"
-xref: delta_mono_mass "26.01565"
-xref: delta_avge_mass "26.0373"
-xref: delta_composition "H(2) C(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:16:03"
-xref: date_time_modified "2006-11-09 10:16:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:544
-name: Ala->Gly
-def: "Ala->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=544]
-xref: record_id "544"
-xref: delta_mono_mass "-14.01565"
-xref: delta_avge_mass "-14.0266"
-xref: delta_composition "H(-2) C(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:16:35"
-xref: date_time_modified "2006-11-09 10:16:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:545
-name: Ala->Glu
-def: "Ala->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=545]
-xref: record_id "545"
-xref: delta_mono_mass "58.005479"
-xref: delta_avge_mass "58.0361"
-xref: delta_composition "H(2) C(2) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:19:56"
-xref: date_time_modified "2006-11-09 10:19:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:546
-name: Ala->Val
-def: "Ala->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=546]
-xref: record_id "546"
-xref: delta_mono_mass "28.0313"
-xref: delta_avge_mass "28.0532"
-xref: delta_composition "H(4) C(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:20:15"
-xref: date_time_modified "2006-11-09 10:20:15"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:547
-name: Cys->Phe
-def: "Cys->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=547]
-xref: record_id "547"
-xref: delta_mono_mass "44.059229"
-xref: delta_avge_mass "44.031"
-xref: delta_composition "H(4) C(6) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:20:41"
-xref: date_time_modified "2006-11-09 10:20:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:548
-name: Cys->Ser
-def: "Cys->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=548]
-xref: record_id "548"
-xref: delta_mono_mass "-15.977156"
-xref: delta_avge_mass "-16.0656"
-xref: delta_composition "O S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:21:13"
-xref: date_time_modified "2006-11-09 10:21:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:549
-name: Cys->Trp
-def: "Cys->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=549]
-xref: record_id "549"
-xref: delta_mono_mass "83.070128"
-xref: delta_avge_mass "83.067"
-xref: delta_composition "H(5) C(8) N S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:21:37"
-xref: date_time_modified "2006-11-09 10:21:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:550
-name: Cys->Tyr
-def: "Cys->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=550]
-xref: record_id "550"
-xref: delta_mono_mass "60.054144"
-xref: delta_avge_mass "60.0304"
-xref: delta_composition "H(4) C(6) O S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:22:04"
-xref: date_time_modified "2006-11-09 10:22:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:551
-name: Cys->Arg
-def: "Cys->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=551]
-xref: record_id "551"
-xref: delta_mono_mass "53.091927"
-xref: delta_avge_mass "53.0428"
-xref: delta_composition "H(7) C(3) N(3) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:22:25"
-xref: date_time_modified "2006-11-09 10:22:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:552
-name: Cys->Gly
-def: "Cys->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=552]
-xref: record_id "552"
-xref: delta_mono_mass "-45.987721"
-xref: delta_avge_mass "-46.0916"
-xref: delta_composition "H(-2) C(-1) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:22:43"
-xref: date_time_modified "2006-11-09 10:22:43"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:553
-name: Asp->Ala
-def: "Asp->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=553]
-xref: record_id "553"
-xref: delta_mono_mass "-43.989829"
-xref: delta_avge_mass "-44.0095"
-xref: delta_composition "C(-1) O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:53:54"
-xref: date_time_modified "2006-11-09 10:53:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:554
-name: Asp->His
-def: "Asp->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=554]
-xref: record_id "554"
-xref: delta_mono_mass "22.031969"
-xref: delta_avge_mass "22.0519"
-xref: delta_composition "H(2) C(2) N(2) O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:55:25"
-xref: date_time_modified "2006-11-09 10:55:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:555
-name: Asp->Asn
-def: "Asp->Asn substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=555]
-xref: record_id "555"
-xref: delta_mono_mass "-0.984016"
-xref: delta_avge_mass "-0.9848"
-xref: delta_composition "H N O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:55:49"
-xref: date_time_modified "2006-11-09 10:55:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:556
-name: Asp->Gly
-def: "Asp->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=556]
-xref: record_id "556"
-xref: delta_mono_mass "-58.005479"
-xref: delta_avge_mass "-58.0361"
-xref: delta_composition "H(-2) C(-2) O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:56:52"
-xref: date_time_modified "2006-11-09 10:56:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:557
-name: Asp->Tyr
-def: "Asp->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=557]
-xref: record_id "557"
-xref: delta_mono_mass "48.036386"
-xref: delta_avge_mass "48.0859"
-xref: delta_composition "H(4) C(5) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:58:23"
-xref: date_time_modified "2006-11-09 10:58:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:558
-name: Asp->Glu
-def: "Asp->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=558]
-xref: record_id "558"
-xref: delta_mono_mass "14.01565"
-xref: delta_avge_mass "14.0266"
-xref: delta_composition "H(2) C"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:58:44"
-xref: date_time_modified "2006-11-09 10:58:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:559
-name: Asp->Val
-def: "Asp->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=559]
-xref: record_id "559"
-xref: delta_mono_mass "-15.958529"
-xref: delta_avge_mass "-15.9563"
-xref: delta_composition "H(4) C O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:59:02"
-xref: date_time_modified "2006-11-09 10:59:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:560
-name: Glu->Ala
-def: "Glu->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=560]
-xref: record_id "560"
-xref: delta_mono_mass "-58.005479"
-xref: delta_avge_mass "-58.0361"
-xref: delta_composition "H(-2) C(-2) O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:00:54"
-xref: date_time_modified "2006-11-09 11:00:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:561
-name: Glu->Gln
-def: "Glu->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=561]
-xref: record_id "561"
-xref: delta_mono_mass "-0.984016"
-xref: delta_avge_mass "-0.9848"
-xref: delta_composition "H N O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:01:29"
-xref: date_time_modified "2006-11-09 11:01:29"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:562
-name: Glu->Asp
-def: "Glu->Asp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=562]
-xref: record_id "562"
-xref: delta_mono_mass "-14.01565"
-xref: delta_avge_mass "-14.0266"
-xref: delta_composition "H(-2) C(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:01:53"
-xref: date_time_modified "2006-11-09 11:01:53"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:563
-name: Glu->Lys
-def: "Glu->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=563]
-xref: record_id "563"
-xref: delta_mono_mass "-0.94763"
-xref: delta_avge_mass "-0.9417"
-xref: delta_composition "H(5) C N O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:02:15"
-xref: date_time_modified "2006-11-09 11:02:15"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:564
-name: Glu->Gly
-def: "Glu->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=564]
-xref: record_id "564"
-xref: delta_mono_mass "-72.021129"
-xref: delta_avge_mass "-72.0627"
-xref: delta_composition "H(-4) C(-3) O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:02:36"
-xref: date_time_modified "2006-11-09 11:02:36"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:565
-name: Glu->Val
-def: "Glu->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=565]
-xref: record_id "565"
-xref: delta_mono_mass "-29.974179"
-xref: delta_avge_mass "-29.9829"
-xref: delta_composition "H(2) O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:03:02"
-xref: date_time_modified "2006-11-09 11:03:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:566
-name: Phe->Ser
-def: "Phe->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=566]
-xref: record_id "566"
-xref: delta_mono_mass "-60.036386"
-xref: delta_avge_mass "-60.0966"
-xref: delta_composition "H(-4) C(-6) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:03:29"
-xref: date_time_modified "2006-11-09 11:03:29"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:567
-name: Phe->Cys
-def: "Phe->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=567]
-xref: record_id "567"
-xref: delta_mono_mass "-44.059229"
-xref: delta_avge_mass "-44.031"
-xref: delta_composition "H(-4) C(-6) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:04:01"
-xref: date_time_modified "2006-11-09 11:04:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:568
-name: Phe->Xle
-def: "Phe->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=568]
-xref: record_id "568"
-xref: delta_mono_mass "-33.98435"
-xref: delta_avge_mass "-34.0162"
-xref: delta_composition "H(2) C(-3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:05:41"
-xref: date_time_modified "2011-06-21 15:10:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:569
-name: Phe->Tyr
-def: "Phe->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=569]
-xref: record_id "569"
-xref: delta_mono_mass "15.994915"
-xref: delta_avge_mass "15.9994"
-xref: delta_composition "O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:06:56"
-xref: date_time_modified "2006-11-09 11:06:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:570
-name: Phe->Val
-def: "Phe->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=570]
-xref: record_id "570"
-xref: delta_mono_mass "-48"
-xref: delta_avge_mass "-48.0428"
-xref: delta_composition "C(-4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:07:20"
-xref: date_time_modified "2006-11-09 11:07:20"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:571
-name: Gly->Ala
-def: "Gly->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=571]
-xref: record_id "571"
-xref: delta_mono_mass "14.01565"
-xref: delta_avge_mass "14.0266"
-xref: delta_composition "H(2) C"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:07:51"
-xref: date_time_modified "2006-11-09 11:07:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:572
-name: Gly->Ser
-def: "Gly->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=572]
-xref: record_id "572"
-xref: delta_mono_mass "30.010565"
-xref: delta_avge_mass "30.026"
-xref: delta_composition "H(2) C O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:08:13"
-xref: date_time_modified "2006-11-09 11:08:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:573
-name: Gly->Trp
-def: "Gly->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=573]
-xref: record_id "573"
-xref: delta_mono_mass "129.057849"
-xref: delta_avge_mass "129.1586"
-xref: delta_composition "H(7) C(9) N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:08:33"
-xref: date_time_modified "2006-11-09 11:08:33"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:574
-name: Gly->Glu
-def: "Gly->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=574]
-xref: record_id "574"
-xref: delta_mono_mass "72.021129"
-xref: delta_avge_mass "72.0627"
-xref: delta_composition "H(4) C(3) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:08:57"
-xref: date_time_modified "2006-11-09 11:08:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:575
-name: Gly->Val
-def: "Gly->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=575]
-xref: record_id "575"
-xref: delta_mono_mass "42.04695"
-xref: delta_avge_mass "42.0797"
-xref: delta_composition "H(6) C(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:09:18"
-xref: date_time_modified "2006-11-09 11:09:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:576
-name: Gly->Asp
-def: "Gly->Asp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=576]
-xref: record_id "576"
-xref: delta_mono_mass "58.005479"
-xref: delta_avge_mass "58.0361"
-xref: delta_composition "H(2) C(2) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:09:44"
-xref: date_time_modified "2006-11-09 11:09:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:577
-name: Gly->Cys
-def: "Gly->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=577]
-xref: record_id "577"
-xref: delta_mono_mass "45.987721"
-xref: delta_avge_mass "46.0916"
-xref: delta_composition "H(2) C S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:10:03"
-xref: date_time_modified "2006-11-09 11:10:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:578
-name: Gly->Arg
-def: "Gly->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=578]
-xref: record_id "578"
-xref: delta_mono_mass "99.079647"
-xref: delta_avge_mass "99.1344"
-xref: delta_composition "H(9) C(4) N(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:10:23"
-xref: date_time_modified "2006-11-09 11:10:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:580
-name: His->Pro
-def: "His->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=580]
-xref: record_id "580"
-xref: delta_mono_mass "-40.006148"
-xref: delta_avge_mass "-40.0241"
-xref: delta_composition "C(-1) N(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:11:29"
-xref: date_time_modified "2006-11-09 11:11:29"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:581
-name: His->Tyr
-def: "His->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=581]
-xref: record_id "581"
-xref: delta_mono_mass "26.004417"
-xref: delta_avge_mass "26.034"
-xref: delta_composition "H(2) C(3) N(-2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:11:50"
-xref: date_time_modified "2006-11-09 11:11:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:582
-name: His->Gln
-def: "His->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=582]
-xref: record_id "582"
-xref: delta_mono_mass "-9.000334"
-xref: delta_avge_mass "-9.0101"
-xref: delta_composition "H C(-1) N(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:14:42"
-xref: date_time_modified "2006-11-09 11:14:42"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:584
-name: His->Arg
-def: "His->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=584]
-xref: record_id "584"
-xref: delta_mono_mass "19.042199"
-xref: delta_avge_mass "19.0464"
-xref: delta_composition "H(5) N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:15:26"
-xref: date_time_modified "2006-11-09 11:15:26"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:585
-name: His->Xle
-def: "His->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=585]
-xref: record_id "585"
-xref: delta_mono_mass "-23.974848"
-xref: delta_avge_mass "-23.9816"
-xref: delta_composition "H(4) N(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:15:51"
-xref: date_time_modified "2011-06-21 15:10:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:588
-name: Xle->Thr
-def: "Leu/Ile->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=588]
-xref: record_id "588"
-xref: delta_mono_mass "-12.036386"
-xref: delta_avge_mass "-12.0538"
-xref: delta_composition "H(-4) C(-2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:18:09"
-xref: date_time_modified "2011-06-21 15:29:22"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "I"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "L"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:589
-name: Xle->Asn
-def: "Leu/Ile->Asn substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=589]
-xref: record_id "589"
-xref: delta_mono_mass "0.958863"
-xref: delta_avge_mass "0.945"
-xref: delta_composition "H(-5) C(-2) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:18:31"
-xref: date_time_modified "2011-06-21 15:29:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "I"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "L"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:590
-name: Xle->Lys
-def: "Leu/Ile->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=590]
-xref: record_id "590"
-xref: delta_mono_mass "15.010899"
-xref: delta_avge_mass "15.0146"
-xref: delta_composition "H N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:18:57"
-xref: date_time_modified "2011-06-21 15:27:59"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "I"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "L"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:594
-name: Lys->Thr
-def: "Lys->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=594]
-xref: record_id "594"
-xref: delta_mono_mass "-27.047285"
-xref: delta_avge_mass "-27.0684"
-xref: delta_composition "H(-5) C(-2) N(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:20:28"
-xref: date_time_modified "2006-11-09 11:20:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:595
-name: Lys->Asn
-def: "Lys->Asn substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=595]
-xref: record_id "595"
-xref: delta_mono_mass "-14.052036"
-xref: delta_avge_mass "-14.0696"
-xref: delta_composition "H(-6) C(-2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:20:51"
-xref: date_time_modified "2006-11-09 11:20:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:596
-name: Lys->Glu
-def: "Lys->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=596]
-xref: record_id "596"
-xref: delta_mono_mass "0.94763"
-xref: delta_avge_mass "0.9417"
-xref: delta_composition "H(-5) C(-1) N(-1) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:21:12"
-xref: date_time_modified "2006-11-09 11:21:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:597
-name: Lys->Gln
-def: "Lys->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=597]
-xref: record_id "597"
-xref: delta_mono_mass "-0.036386"
-xref: delta_avge_mass "-0.0431"
-xref: delta_composition "H(-4) C(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:21:32"
-xref: date_time_modified "2006-11-09 11:21:32"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:598
-name: Lys->Met
-def: "Lys->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=598]
-xref: record_id "598"
-xref: delta_mono_mass "2.945522"
-xref: delta_avge_mass "3.0238"
-xref: delta_composition "H(-3) C(-1) N(-1) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:21:56"
-xref: date_time_modified "2006-11-09 11:21:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:599
-name: Lys->Arg
-def: "Lys->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=599]
-xref: record_id "599"
-xref: delta_mono_mass "28.006148"
-xref: delta_avge_mass "28.0134"
-xref: delta_composition "N(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:22:15"
-xref: date_time_modified "2006-11-09 11:22:15"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:600
-name: Lys->Xle
-def: "Lys->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=600]
-xref: record_id "600"
-xref: delta_mono_mass "-15.010899"
-xref: delta_avge_mass "-15.0146"
-xref: delta_composition "H(-1) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:22:38"
-xref: date_time_modified "2011-06-21 15:25:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:601
-name: Xle->Ser
-def: "Leu/Ile->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=601]
-xref: record_id "601"
-xref: delta_mono_mass "-26.052036"
-xref: delta_avge_mass "-26.0803"
-xref: delta_composition "H(-6) C(-3) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:23:01"
-xref: date_time_modified "2011-06-21 15:29:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "I"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:602
-name: Xle->Phe
-def: "Leu/Ile->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=602]
-xref: record_id "602"
-xref: delta_mono_mass "33.98435"
-xref: delta_avge_mass "34.0162"
-xref: delta_composition "H(-2) C(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:23:22"
-xref: date_time_modified "2011-06-21 15:28:53"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "I"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:603
-name: Xle->Trp
-def: "Leu/Ile->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=603]
-xref: record_id "603"
-xref: delta_mono_mass "72.995249"
-xref: delta_avge_mass "73.0523"
-xref: delta_composition "H(-1) C(5) N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:23:48"
-xref: date_time_modified "2011-06-21 15:28:22"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "I"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:604
-name: Xle->Pro
-def: "Leu/Ile->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=604]
-xref: record_id "604"
-xref: delta_mono_mass "-16.0313"
-xref: delta_avge_mass "-16.0425"
-xref: delta_composition "H(-4) C(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:24:06"
-xref: date_time_modified "2011-06-21 15:29:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "I"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:605
-name: Xle->Val
-def: "Leu/Ile->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=605]
-xref: record_id "605"
-xref: delta_mono_mass "-14.01565"
-xref: delta_avge_mass "-14.0266"
-xref: delta_composition "H(-2) C(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:24:28"
-xref: date_time_modified "2011-06-21 15:28:33"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "I"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:606
-name: Xle->His
-def: "Leu/Ile->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=606]
-xref: record_id "606"
-xref: delta_mono_mass "23.974848"
-xref: delta_avge_mass "23.9816"
-xref: delta_composition "H(-4) N(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:24:50"
-xref: date_time_modified "2011-06-21 15:29:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "I"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:607
-name: Xle->Gln
-def: "Leu/Ile->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=607]
-xref: record_id "607"
-xref: delta_mono_mass "14.974514"
-xref: delta_avge_mass "14.9716"
-xref: delta_composition "H(-3) C(-1) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:25:14"
-xref: date_time_modified "2011-06-21 15:29:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "I"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:608
-name: Xle->Met
-def: "Leu/Ile->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=608]
-xref: record_id "608"
-xref: delta_mono_mass "17.956421"
-xref: delta_avge_mass "18.0384"
-xref: delta_composition "H(-2) C(-1) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:25:59"
-xref: date_time_modified "2011-06-21 15:28:43"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "I"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:609
-name: Xle->Arg
-def: "Leu/Ile->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=609]
-xref: record_id "609"
-xref: delta_mono_mass "43.017047"
-xref: delta_avge_mass "43.028"
-xref: delta_composition "H N(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:26:21"
-xref: date_time_modified "2011-06-21 15:28:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "I"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:610
-name: Met->Thr
-def: "Met->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=610]
-xref: record_id "610"
-xref: delta_mono_mass "-29.992806"
-xref: delta_avge_mass "-30.0922"
-xref: delta_composition "H(-2) C(-1) O S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:26:47"
-xref: date_time_modified "2006-11-09 11:26:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:611
-name: Met->Arg
-def: "Met->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=611]
-xref: record_id "611"
-xref: delta_mono_mass "25.060626"
-xref: delta_avge_mass "24.9896"
-xref: delta_composition "H(3) C N(3) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:27:10"
-xref: date_time_modified "2006-11-09 11:27:10"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:613
-name: Met->Lys
-def: "Met->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=613]
-xref: record_id "613"
-xref: delta_mono_mass "-2.945522"
-xref: delta_avge_mass "-3.0238"
-xref: delta_composition "H(3) C N S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:28:29"
-xref: date_time_modified "2006-11-09 11:28:29"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:614
-name: Met->Xle
-def: "Met->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=614]
-synonym: "Also Met->norleucine" RELATED []
-xref: record_id "614"
-xref: delta_mono_mass "-17.956421"
-xref: delta_avge_mass "-18.0384"
-xref: delta_composition "H(2) C S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:28:56"
-xref: date_time_modified "2018-02-28 16:07:26"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:615
-name: Met->Val
-def: "Met->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=615]
-xref: record_id "615"
-xref: delta_mono_mass "-31.972071"
-xref: delta_avge_mass "-32.065"
-xref: delta_composition "S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:29:27"
-xref: date_time_modified "2006-11-09 11:29:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:616
-name: Asn->Ser
-def: "Asn->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=616]
-xref: record_id "616"
-xref: delta_mono_mass "-27.010899"
-xref: delta_avge_mass "-27.0253"
-xref: delta_composition "H(-1) C(-1) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:29:57"
-xref: date_time_modified "2006-11-09 11:29:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:617
-name: Asn->Thr
-def: "Asn->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=617]
-xref: record_id "617"
-xref: delta_mono_mass "-12.995249"
-xref: delta_avge_mass "-12.9988"
-xref: delta_composition "H N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:34:11"
-xref: date_time_modified "2006-11-09 11:34:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:618
-name: Asn->Lys
-def: "Asn->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=618]
-xref: record_id "618"
-xref: delta_mono_mass "14.052036"
-xref: delta_avge_mass "14.0696"
-xref: delta_composition "H(6) C(2) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:34:31"
-xref: date_time_modified "2006-11-09 11:34:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:619
-name: Asn->Tyr
-def: "Asn->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=619]
-xref: record_id "619"
-xref: delta_mono_mass "49.020401"
-xref: delta_avge_mass "49.0706"
-xref: delta_composition "H(3) C(5) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:34:56"
-xref: date_time_modified "2006-11-09 11:34:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:620
-name: Asn->His
-def: "Asn->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=620]
-xref: record_id "620"
-xref: delta_mono_mass "23.015984"
-xref: delta_avge_mass "23.0366"
-xref: delta_composition "H C(2) N O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:35:18"
-xref: date_time_modified "2006-11-09 11:35:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:621
-name: Asn->Asp
-def: "Asn->Asp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=621]
-xref: record_id "621"
-xref: delta_mono_mass "0.984016"
-xref: delta_avge_mass "0.9848"
-xref: delta_composition "H(-1) N(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:35:42"
-xref: date_time_modified "2006-11-09 11:35:42"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:622
-name: Asn->Xle
-def: "Asn->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=622]
-xref: record_id "622"
-xref: delta_mono_mass "-0.958863"
-xref: delta_avge_mass "-0.945"
-xref: delta_composition "H(5) C(2) N(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:36:02"
-xref: date_time_modified "2011-06-21 15:13:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:623
-name: Pro->Ser
-def: "Pro->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=623]
-xref: record_id "623"
-xref: delta_mono_mass "-10.020735"
-xref: delta_avge_mass "-10.0379"
-xref: delta_composition "H(-2) C(-2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:36:26"
-xref: date_time_modified "2006-11-09 11:36:26"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:624
-name: Pro->Ala
-def: "Pro->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=624]
-xref: record_id "624"
-xref: delta_mono_mass "-26.01565"
-xref: delta_avge_mass "-26.0373"
-xref: delta_composition "H(-2) C(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:37:56"
-xref: date_time_modified "2006-11-09 11:37:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:625
-name: Pro->His
-def: "Pro->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=625]
-xref: record_id "625"
-xref: delta_mono_mass "40.006148"
-xref: delta_avge_mass "40.0241"
-xref: delta_composition "C N(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:38:18"
-xref: date_time_modified "2006-11-09 11:38:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:626
-name: Pro->Gln
-def: "Pro->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=626]
-xref: record_id "626"
-xref: delta_mono_mass "31.005814"
-xref: delta_avge_mass "31.014"
-xref: delta_composition "H N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:38:40"
-xref: date_time_modified "2006-11-09 11:38:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:627
-name: Pro->Thr
-def: "Pro->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=627]
-xref: record_id "627"
-xref: delta_mono_mass "3.994915"
-xref: delta_avge_mass "3.9887"
-xref: delta_composition "C(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:39:02"
-xref: date_time_modified "2006-11-09 11:39:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:628
-name: Pro->Arg
-def: "Pro->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=628]
-xref: record_id "628"
-xref: delta_mono_mass "59.048347"
-xref: delta_avge_mass "59.0705"
-xref: delta_composition "H(5) C N(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:39:29"
-xref: date_time_modified "2006-11-09 11:39:29"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:629
-name: Pro->Xle
-def: "Pro->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=629]
-xref: record_id "629"
-xref: delta_mono_mass "16.0313"
-xref: delta_avge_mass "16.0425"
-xref: delta_composition "H(4) C"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:39:47"
-xref: date_time_modified "2011-06-21 15:09:36"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:630
-name: Gln->Pro
-def: "Gln->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=630]
-xref: record_id "630"
-xref: delta_mono_mass "-31.005814"
-xref: delta_avge_mass "-31.014"
-xref: delta_composition "H(-1) N(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:40:19"
-xref: date_time_modified "2006-11-09 11:40:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:631
-name: Gln->Lys
-def: "Gln->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=631]
-xref: record_id "631"
-xref: delta_mono_mass "0.036386"
-xref: delta_avge_mass "0.0431"
-xref: delta_composition "H(4) C O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:42:17"
-xref: date_time_modified "2006-11-09 11:42:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:632
-name: Gln->Glu
-def: "Gln->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=632]
-xref: record_id "632"
-xref: delta_mono_mass "0.984016"
-xref: delta_avge_mass "0.9848"
-xref: delta_composition "H(-1) N(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:42:38"
-xref: date_time_modified "2006-11-09 11:42:38"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:633
-name: Gln->His
-def: "Gln->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=633]
-xref: record_id "633"
-xref: delta_mono_mass "9.000334"
-xref: delta_avge_mass "9.0101"
-xref: delta_composition "H(-1) C N O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:42:58"
-xref: date_time_modified "2006-11-09 11:42:58"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:634
-name: Gln->Arg
-def: "Gln->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=634]
-xref: record_id "634"
-xref: delta_mono_mass "28.042534"
-xref: delta_avge_mass "28.0565"
-xref: delta_composition "H(4) C N(2) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:43:25"
-xref: date_time_modified "2006-11-09 11:43:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:635
-name: Gln->Xle
-def: "Gln->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=635]
-xref: record_id "635"
-xref: delta_mono_mass "-14.974514"
-xref: delta_avge_mass "-14.9716"
-xref: delta_composition "H(3) C N(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:43:47"
-xref: date_time_modified "2011-06-21 15:09:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:636
-name: Arg->Ser
-def: "Arg->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=636]
-xref: record_id "636"
-xref: delta_mono_mass "-69.069083"
-xref: delta_avge_mass "-69.1084"
-xref: delta_composition "H(-7) C(-3) N(-3) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:44:13"
-xref: date_time_modified "2006-11-09 11:44:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:637
-name: Arg->Trp
-def: "Arg->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=637]
-xref: record_id "637"
-xref: delta_mono_mass "29.978202"
-xref: delta_avge_mass "30.0242"
-xref: delta_composition "H(-2) C(5) N(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:44:36"
-xref: date_time_modified "2006-11-09 11:44:36"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:638
-name: Arg->Thr
-def: "Arg->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=638]
-xref: record_id "638"
-xref: delta_mono_mass "-55.053433"
-xref: delta_avge_mass "-55.0818"
-xref: delta_composition "H(-5) C(-2) N(-3) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:44:59"
-xref: date_time_modified "2006-11-09 11:44:59"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:639
-name: Arg->Pro
-def: "Arg->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=639]
-xref: record_id "639"
-xref: delta_mono_mass "-59.048347"
-xref: delta_avge_mass "-59.0705"
-xref: delta_composition "H(-5) C(-1) N(-3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:45:18"
-xref: date_time_modified "2006-11-09 11:45:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:640
-name: Arg->Lys
-def: "Arg->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=640]
-xref: record_id "640"
-xref: delta_mono_mass "-28.006148"
-xref: delta_avge_mass "-28.0134"
-xref: delta_composition "N(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:45:37"
-xref: date_time_modified "2006-11-09 11:45:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:641
-name: Arg->His
-def: "Arg->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=641]
-xref: record_id "641"
-xref: delta_mono_mass "-19.042199"
-xref: delta_avge_mass "-19.0464"
-xref: delta_composition "H(-5) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:45:56"
-xref: date_time_modified "2006-11-09 11:45:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:642
-name: Arg->Gln
-def: "Arg->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=642]
-xref: record_id "642"
-xref: delta_mono_mass "-28.042534"
-xref: delta_avge_mass "-28.0565"
-xref: delta_composition "H(-4) C(-1) N(-2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:46:17"
-xref: date_time_modified "2006-11-09 11:46:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:643
-name: Arg->Met
-def: "Arg->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=643]
-xref: record_id "643"
-xref: delta_mono_mass "-25.060626"
-xref: delta_avge_mass "-24.9896"
-xref: delta_composition "H(-3) C(-1) N(-3) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:46:37"
-xref: date_time_modified "2006-11-09 11:46:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:644
-name: Arg->Cys
-def: "Arg->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=644]
-xref: record_id "644"
-xref: delta_mono_mass "-53.091927"
-xref: delta_avge_mass "-53.0428"
-xref: delta_composition "H(-7) C(-3) N(-3) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:47:00"
-xref: date_time_modified "2006-11-09 11:47:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:645
-name: Arg->Xle
-def: "Arg->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=645]
-xref: record_id "645"
-xref: delta_mono_mass "-43.017047"
-xref: delta_avge_mass "-43.028"
-xref: delta_composition "H(-1) N(-3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:47:36"
-xref: date_time_modified "2011-06-21 15:09:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:646
-name: Arg->Gly
-def: "Arg->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=646]
-xref: record_id "646"
-xref: delta_mono_mass "-99.079647"
-xref: delta_avge_mass "-99.1344"
-xref: delta_composition "H(-9) C(-4) N(-3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:48:00"
-xref: date_time_modified "2006-11-09 11:48:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:647
-name: Ser->Phe
-def: "Ser->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=647]
-xref: record_id "647"
-xref: delta_mono_mass "60.036386"
-xref: delta_avge_mass "60.0966"
-xref: delta_composition "H(4) C(6) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:32:55"
-xref: date_time_modified "2006-11-09 12:32:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:648
-name: Ser->Ala
-def: "Ser->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=648]
-xref: record_id "648"
-xref: delta_mono_mass "-15.994915"
-xref: delta_avge_mass "-15.9994"
-xref: delta_composition "O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:33:14"
-xref: date_time_modified "2006-11-09 12:33:14"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:649
-name: Ser->Trp
-def: "Ser->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=649]
-xref: record_id "649"
-xref: delta_mono_mass "99.047285"
-xref: delta_avge_mass "99.1326"
-xref: delta_composition "H(5) C(8) N O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:33:32"
-xref: date_time_modified "2006-11-09 12:33:32"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:650
-name: Ser->Thr
-def: "Ser->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=650]
-xref: record_id "650"
-xref: delta_mono_mass "14.01565"
-xref: delta_avge_mass "14.0266"
-xref: delta_composition "H(2) C"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:33:51"
-xref: date_time_modified "2006-11-09 12:33:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:651
-name: Ser->Asn
-def: "Ser->Asn substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=651]
-xref: record_id "651"
-xref: delta_mono_mass "27.010899"
-xref: delta_avge_mass "27.0253"
-xref: delta_composition "H C N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:34:12"
-xref: date_time_modified "2006-11-09 12:34:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:652
-name: Ser->Pro
-def: "Ser->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=652]
-xref: record_id "652"
-xref: delta_mono_mass "10.020735"
-xref: delta_avge_mass "10.0379"
-xref: delta_composition "H(2) C(2) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:34:34"
-xref: date_time_modified "2006-11-09 12:34:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:653
-name: Ser->Tyr
-def: "Ser->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=653]
-xref: record_id "653"
-xref: delta_mono_mass "76.0313"
-xref: delta_avge_mass "76.096"
-xref: delta_composition "H(4) C(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:35:00"
-xref: date_time_modified "2006-11-09 12:35:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:654
-name: Ser->Cys
-def: "Ser->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=654]
-xref: record_id "654"
-xref: delta_mono_mass "15.977156"
-xref: delta_avge_mass "16.0656"
-xref: delta_composition "O(-1) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:35:22"
-xref: date_time_modified "2006-11-09 12:35:22"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:655
-name: Ser->Arg
-def: "Ser->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=655]
-xref: record_id "655"
-xref: delta_mono_mass "69.069083"
-xref: delta_avge_mass "69.1084"
-xref: delta_composition "H(7) C(3) N(3) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:35:40"
-xref: date_time_modified "2006-11-09 12:35:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:656
-name: Ser->Xle
-def: "Ser->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=656]
-xref: record_id "656"
-xref: delta_mono_mass "26.052036"
-xref: delta_avge_mass "26.0803"
-xref: delta_composition "H(6) C(3) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:36:10"
-xref: date_time_modified "2011-06-21 15:08:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:657
-name: Ser->Gly
-def: "Ser->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=657]
-xref: record_id "657"
-xref: delta_mono_mass "-30.010565"
-xref: delta_avge_mass "-30.026"
-xref: delta_composition "H(-2) C(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:36:34"
-xref: date_time_modified "2006-11-09 12:36:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:658
-name: Thr->Ser
-def: "Thr->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=658]
-xref: record_id "658"
-xref: delta_mono_mass "-14.01565"
-xref: delta_avge_mass "-14.0266"
-xref: delta_composition "H(-2) C(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:36:57"
-xref: date_time_modified "2006-11-09 12:36:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:659
-name: Thr->Ala
-def: "Thr->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=659]
-xref: record_id "659"
-xref: delta_mono_mass "-30.010565"
-xref: delta_avge_mass "-30.026"
-xref: delta_composition "H(-2) C(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:37:15"
-xref: date_time_modified "2006-11-09 12:37:15"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:660
-name: Thr->Asn
-def: "Thr->Asn substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=660]
-xref: record_id "660"
-xref: delta_mono_mass "12.995249"
-xref: delta_avge_mass "12.9988"
-xref: delta_composition "H(-1) N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:37:37"
-xref: date_time_modified "2006-11-09 12:37:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:661
-name: Thr->Lys
-def: "Thr->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=661]
-xref: record_id "661"
-xref: delta_mono_mass "27.047285"
-xref: delta_avge_mass "27.0684"
-xref: delta_composition "H(5) C(2) N O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:37:55"
-xref: date_time_modified "2006-11-09 12:37:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:662
-name: Thr->Pro
-def: "Thr->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=662]
-xref: record_id "662"
-xref: delta_mono_mass "-3.994915"
-xref: delta_avge_mass "-3.9887"
-xref: delta_composition "C O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:38:14"
-xref: date_time_modified "2006-11-09 12:38:14"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:663
-name: Thr->Met
-def: "Thr->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=663]
-xref: record_id "663"
-xref: delta_mono_mass "29.992806"
-xref: delta_avge_mass "30.0922"
-xref: delta_composition "H(2) C O(-1) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:38:34"
-xref: date_time_modified "2006-11-09 12:38:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:664
-name: Thr->Xle
-def: "Thr->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=664]
-xref: record_id "664"
-xref: delta_mono_mass "12.036386"
-xref: delta_avge_mass "12.0538"
-xref: delta_composition "H(4) C(2) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:38:56"
-xref: date_time_modified "2011-06-21 15:25:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:665
-name: Thr->Arg
-def: "Thr->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=665]
-xref: record_id "665"
-xref: delta_mono_mass "55.053433"
-xref: delta_avge_mass "55.0818"
-xref: delta_composition "H(5) C(2) N(3) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:39:14"
-xref: date_time_modified "2006-11-09 12:39:14"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:666
-name: Val->Phe
-def: "Val->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=666]
-xref: record_id "666"
-xref: delta_mono_mass "48"
-xref: delta_avge_mass "48.0428"
-xref: delta_composition "C(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:39:35"
-xref: date_time_modified "2006-11-09 12:39:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:667
-name: Val->Ala
-def: "Val->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=667]
-xref: record_id "667"
-xref: delta_mono_mass "-28.0313"
-xref: delta_avge_mass "-28.0532"
-xref: delta_composition "H(-4) C(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:40:00"
-xref: date_time_modified "2006-11-09 12:40:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:668
-name: Val->Glu
-def: "Val->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=668]
-xref: record_id "668"
-xref: delta_mono_mass "29.974179"
-xref: delta_avge_mass "29.9829"
-xref: delta_composition "H(-2) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:40:19"
-xref: date_time_modified "2006-11-09 12:40:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:669
-name: Val->Met
-def: "Val->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=669]
-xref: record_id "669"
-xref: delta_mono_mass "31.972071"
-xref: delta_avge_mass "32.065"
-xref: delta_composition "S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:40:36"
-xref: date_time_modified "2006-11-09 12:40:36"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:670
-name: Val->Asp
-def: "Val->Asp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=670]
-xref: record_id "670"
-xref: delta_mono_mass "15.958529"
-xref: delta_avge_mass "15.9563"
-xref: delta_composition "H(-4) C(-1) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:41:04"
-xref: date_time_modified "2006-11-09 12:41:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:671
-name: Val->Xle
-def: "Val->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=671]
-xref: record_id "671"
-xref: delta_mono_mass "14.01565"
-xref: delta_avge_mass "14.0266"
-xref: delta_composition "H(2) C"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:41:27"
-xref: date_time_modified "2011-06-21 15:08:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:672
-name: Val->Gly
-def: "Val->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=672]
-xref: record_id "672"
-xref: delta_mono_mass "-42.04695"
-xref: delta_avge_mass "-42.0797"
-xref: delta_composition "H(-6) C(-3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:41:45"
-xref: date_time_modified "2006-11-09 12:41:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:673
-name: Trp->Ser
-def: "Trp->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=673]
-xref: record_id "673"
-xref: delta_mono_mass "-99.047285"
-xref: delta_avge_mass "-99.1326"
-xref: delta_composition "H(-5) C(-8) N(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:42:22"
-xref: date_time_modified "2006-11-09 12:42:22"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:674
-name: Trp->Cys
-def: "Trp->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=674]
-xref: record_id "674"
-xref: delta_mono_mass "-83.070128"
-xref: delta_avge_mass "-83.067"
-xref: delta_composition "H(-5) C(-8) N(-1) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:42:46"
-xref: date_time_modified "2006-11-09 12:42:46"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:675
-name: Trp->Arg
-def: "Trp->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=675]
-xref: record_id "675"
-xref: delta_mono_mass "-29.978202"
-xref: delta_avge_mass "-30.0242"
-xref: delta_composition "H(2) C(-5) N(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:43:10"
-xref: date_time_modified "2006-11-09 12:43:10"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:676
-name: Trp->Gly
-def: "Trp->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=676]
-xref: record_id "676"
-xref: delta_mono_mass "-129.057849"
-xref: delta_avge_mass "-129.1586"
-xref: delta_composition "H(-7) C(-9) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:43:29"
-xref: date_time_modified "2006-11-09 12:43:29"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:677
-name: Trp->Xle
-def: "Trp->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=677]
-xref: record_id "677"
-xref: delta_mono_mass "-72.995249"
-xref: delta_avge_mass "-73.0523"
-xref: delta_composition "H C(-5) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:43:49"
-xref: date_time_modified "2011-06-21 15:08:09"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:678
-name: Tyr->Phe
-def: "Tyr->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=678]
-xref: record_id "678"
-xref: delta_mono_mass "-15.994915"
-xref: delta_avge_mass "-15.9994"
-xref: delta_composition "O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:44:13"
-xref: date_time_modified "2006-11-09 12:44:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:679
-name: Tyr->Ser
-def: "Tyr->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=679]
-xref: record_id "679"
-xref: delta_mono_mass "-76.0313"
-xref: delta_avge_mass "-76.096"
-xref: delta_composition "H(-4) C(-6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:44:37"
-xref: date_time_modified "2006-11-09 12:44:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:680
-name: Tyr->Asn
-def: "Tyr->Asn substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=680]
-xref: record_id "680"
-xref: delta_mono_mass "-49.020401"
-xref: delta_avge_mass "-49.0706"
-xref: delta_composition "H(-3) C(-5) N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:44:59"
-xref: date_time_modified "2006-11-09 12:44:59"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:681
-name: Tyr->His
-def: "Tyr->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=681]
-xref: record_id "681"
-xref: delta_mono_mass "-26.004417"
-xref: delta_avge_mass "-26.034"
-xref: delta_composition "H(-2) C(-3) N(2) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:45:22"
-xref: date_time_modified "2006-11-09 12:45:22"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:682
-name: Tyr->Asp
-def: "Tyr->Asp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=682]
-xref: record_id "682"
-xref: delta_mono_mass "-48.036386"
-xref: delta_avge_mass "-48.0859"
-xref: delta_composition "H(-4) C(-5) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:45:44"
-xref: date_time_modified "2006-11-09 12:45:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:683
-name: Tyr->Cys
-def: "Tyr->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=683]
-xref: record_id "683"
-xref: delta_mono_mass "-60.054144"
-xref: delta_avge_mass "-60.0304"
-xref: delta_composition "H(-4) C(-6) O(-1) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:46:03"
-xref: date_time_modified "2006-11-09 12:46:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:684
-name: BDMAPP
-def: "Mass Defect Tag on lysine e-amino." [URL:http\://www.targetdiscovery.com/article.php?topic=crpc.prst&story=20060321132643690, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=684]
-xref: record_id "684"
-xref: delta_mono_mass "253.010225"
-xref: delta_avge_mass "254.1231"
-xref: delta_composition "H(12) C(11) N O Br"
-xref: username_of_poster "LVSchneid"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-13 18:51:11"
-xref: date_time_modified "2006-11-13 18:52:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_misc_notes "Low efficiency"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "Y"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Artefact"
-xref: spec_4_misc_notes "Low efficiency"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "W"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Artefact"
-xref: spec_5_misc_notes "Low efficiency"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:685
-name: NA-LNO2
-def: "Nitroalkylation by Nitro Linoleic Acid." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=685]
-comment: Reversible post-translational modification of proteins by nitrated fatty acids.
-synonym: "Michael addition of nitro-linoleic acid to Cys and His" RELATED []
-xref: record_id "685"
-xref: delta_mono_mass "325.225309"
-xref: delta_avge_mass "325.443"
-xref: delta_composition "H(31) C(18) N O(4)"
-xref: username_of_poster "cbatthya"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-13 18:59:35"
-xref: date_time_modified "2006-11-13 18:59:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:686
-name: NA-OA-NO2
-def: "Nitroalkylation by Nitro Oleic Acid." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=686]
-comment: Reversible post-translational modification of proteins by nitrated fatty acids.
-synonym: "Michael addition of nitro-oleic acid to Cys and His" RELATED []
-xref: record_id "686"
-xref: delta_mono_mass "327.240959"
-xref: delta_avge_mass "327.4589"
-xref: delta_composition "H(33) C(18) N O(4)"
-xref: username_of_poster "cbatthya"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-13 19:01:33"
-xref: date_time_modified "2006-11-13 19:01:33"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:687
-name: ICPL:2H(4)
-def: "Bruker Daltonics SERVA-ICPL(TM) quantification chemistry, medium form." [URL:http\://www.bdal.de/life-science-tools/care-consumables-more/icpl-kit.html, PMID:15602776, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=687]
-comment: Attention: As the digest is typically applied AFTER ICPL_light/heavy labeling, only ProteinN-term labeling and Lys-specific labeling is applied.
-xref: record_id "687"
-xref: delta_mono_mass "109.046571"
-xref: delta_avge_mass "109.1188"
-xref: delta_composition "H(-1) 2H(4) C(6) N O"
-xref: username_of_poster "suckau"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-13 19:05:12"
-xref: date_time_modified "2008-09-03 15:26:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_2_misc_notes "Use when labelling pre-digest"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Use when labelling post-digest"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:695
-name: Label:13C(6)15N(1)
-def: "13C(6) 15N(1) Silac label." [URL:http\://www.pil.sdu.dk/silac_intro.htm, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=695]
-xref: record_id "695"
-xref: delta_mono_mass "7.017164"
-xref: delta_avge_mass "6.9493"
-xref: delta_composition "C(-6) 13C(6) N(-1) 15N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-29 15:10:53"
-xref: date_time_modified "2007-08-22 18:30:49"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "I"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:696
-name: Label:2H(9)13C(6)15N(2)
-def: "13C(6) 15N(2) (D)9 SILAC label." [URL:http\://www.pil.sdu.dk/silac_intro.htm, URL:http\://www.isotope.com/cil/products/displayproduct.cfm?prod_id=8635, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=696]
-synonym: "heavy D9 lysine" RELATED []
-xref: record_id "696"
-xref: delta_mono_mass "17.07069"
-xref: delta_avge_mass "16.9982"
-xref: delta_composition "H(-9) 2H(9) C(-6) 13C(6) N(-2) 15N(2)"
-xref: username_of_poster "striker2000"
-xref: group_of_poster ""
-xref: date_time_posted "2006-12-01 22:36:25"
-xref: date_time_modified "2007-08-22 18:48:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "Used in SILAC experiment"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:697
-name: NIC
-def: "Nicotinic Acid." [PMID:15004565, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=697]
-xref: record_id "697"
-xref: delta_mono_mass "105.021464"
-xref: delta_avge_mass "105.0941"
-xref: delta_composition "H(3) C(6) N O"
-xref: username_of_poster "verena-meyer"
-xref: group_of_poster ""
-xref: date_time_posted "2006-12-04 16:04:56"
-xref: date_time_modified "2024-08-12 10:05:07"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:698
-name: dNIC
-def: "Deuterated Nicotinic Acid." [PMID:15004565, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=698]
-xref: record_id "698"
-xref: delta_mono_mass "109.048119"
-xref: delta_avge_mass "109.1205"
-xref: delta_composition "H 2H(3) C(6) N O"
-xref: username_of_poster "verena-meyer"
-xref: group_of_poster ""
-xref: date_time_posted "2006-12-04 16:12:54"
-xref: date_time_modified "2024-08-12 10:04:46"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:720
-name: HNE-Delta:H(2)O
-def: "Dehydrated 4-hydroxynonenal." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=720]
-comment: Mass Spectroscopic Characterization of Protein Modification by 4-Hydroxy-2-(E)-nonenal and 4-Oxo-2-(E)-nonenal.
-xref: record_id "720"
-xref: delta_mono_mass "138.104465"
-xref: delta_avge_mass "138.2069"
-xref: delta_composition "H(14) C(9) O"
-xref: username_of_poster "stewartb"
-xref: group_of_poster ""
-xref: date_time_posted "2007-01-08 18:29:46"
-xref: date_time_modified "2007-01-21 18:27:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:721
-name: 4-ONE
-def: "4-Oxononenal (ONE)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=721]
-comment: Covalent adduction of nucleophilic amino acids by 4-hydroxynonenal and 4-oxononenal.
-xref: record_id "721"
-xref: delta_mono_mass "154.09938"
-xref: delta_avge_mass "154.2063"
-xref: delta_composition "H(14) C(9) O(2)"
-xref: username_of_poster "stewartb"
-xref: group_of_poster ""
-xref: date_time_posted "2007-01-08 19:41:28"
-xref: date_time_modified "2007-01-21 18:26:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:723
-name: O-Dimethylphosphate
-def: "O-Dimethylphosphorylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=723]
-xref: record_id "723"
-xref: delta_mono_mass "107.997631"
-xref: delta_avge_mass "108.0331"
-xref: delta_composition "H(5) C(2) O(3) P"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2007-01-09 21:25:28"
-xref: date_time_modified "2007-01-13 21:01:15"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:724
-name: O-Methylphosphate
-def: "O-Methylphosphorylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=724]
-comment: Created by auto-catalytic dealkylation of the O-Dimethylphosphate adduct.
-xref: record_id "724"
-xref: delta_mono_mass "93.981981"
-xref: delta_avge_mass "94.0065"
-xref: delta_composition "H(3) C O(3) P"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2007-01-09 21:35:38"
-xref: date_time_modified "2007-01-21 18:13:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:725
-name: Diethylphosphate
-def: "O-Diethylphosphorylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=725]
-xref: record_id "725"
-xref: delta_mono_mass "136.028931"
-xref: delta_avge_mass "136.0862"
-xref: delta_composition "H(9) C(4) O(3) P"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2007-01-09 21:44:04"
-xref: date_time_modified "2011-12-05 16:15:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "K"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "C"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "H"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "N-term"
-xref: spec_7_position "Any N-term"
-xref: spec_7_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:726
-name: Ethylphosphate
-def: "O-Ethylphosphorylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=726]
-comment: Created by auto-catalytic dealkylation of the O-Diethylphosphate adduct.
-xref: record_id "726"
-xref: delta_mono_mass "107.997631"
-xref: delta_avge_mass "108.0331"
-xref: delta_composition "H(5) C(2) O(3) P"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2007-01-09 21:46:17"
-xref: date_time_modified "2011-12-05 16:15:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "K"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "N-term"
-xref: spec_5_position "Any N-term"
-xref: spec_5_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:727
-name: O-pinacolylmethylphosphonate
-def: "O-pinacolylmethylphosphonylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=727]
-xref: record_id "727"
-xref: delta_mono_mass "162.080967"
-xref: delta_avge_mass "162.1666"
-xref: delta_composition "H(15) C(7) O(2) P"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2007-01-10 16:04:46"
-xref: date_time_modified "2010-04-29 08:38:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "H"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "K"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:728
-name: Methylphosphonate
-def: "Methylphosphonylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=728]
-comment: Created by auto-catalytic dealkylation of either the O-pinacolylmethylphosphonate adduct, or the O-isopropylmethylphosphonate adduct.
-xref: record_id "728"
-xref: delta_mono_mass "77.987066"
-xref: delta_avge_mass "78.0071"
-xref: delta_composition "H(3) C O(2) P"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2007-01-10 16:07:37"
-xref: date_time_modified "2007-01-21 18:11:36"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:729
-name: O-Isopropylmethylphosphonate
-def: "O-Isopropylmethylphosphonylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=729]
-xref: record_id "729"
-xref: delta_mono_mass "120.034017"
-xref: delta_avge_mass "120.0868"
-xref: delta_composition "H(9) C(4) O(2) P"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2007-01-10 16:10:55"
-xref: date_time_modified "2007-01-13 21:02:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:730
-name: iTRAQ8plex
-def: "Representative mass and accurate mass for 113, 114, 116 & 117." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=730]
-comment: Other 4 channels have the same nominal mass but slightly different exact mass. For quantitation purposes, use this entry for all channels.
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry AKA iTRAQ8plex:13C(7)15N(1)" RELATED []
-xref: record_id "730"
-xref: delta_mono_mass "304.20536"
-xref: delta_avge_mass "304.3074"
-xref: delta_composition "H(24) C(7) 13C(7) N(3) 15N O(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2007-01-11 09:53:13"
-xref: date_time_modified "2024-08-12 09:56:06"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "0"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Low abundance"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "H"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "Very low abundance"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "S"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Isotopic label"
-xref: spec_5_misc_notes "Very low abundance"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "T"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Isotopic label"
-xref: spec_6_misc_notes "Very low abundance"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "N-term"
-xref: spec_7_position "Protein N-term"
-xref: spec_7_classification "Isotopic label"
-xref: spec_8_group "8"
-xref: spec_8_hidden "1"
-xref: spec_8_site "C"
-xref: spec_8_position "Anywhere"
-xref: spec_8_classification "Isotopic label"
-xref: spec_8_misc_notes "side reaction"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:731
-name: iTRAQ8plex:13C(6)15N(2)
-def: "Accurate mass for 115, 118, 119 & 121." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=731]
-comment: Other 4 channels have the same nominal mass but slightly different exact mass. For quantitation purposes, use iTRAQ8plex for all channels.
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED []
-xref: record_id "731"
-xref: delta_mono_mass "304.19904"
-xref: delta_avge_mass "304.3081"
-xref: delta_composition "H(24) C(8) 13C(6) N(2) 15N(2) O(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2007-01-11 09:56:21"
-xref: date_time_modified "2024-08-12 09:56:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Low abundance"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "C"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "side reaction"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:734
-name: Ethanolamine
-def: "Carboxyl modification with ethanolamine." [PMID:2, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=734]
-comment: Carbodiimide mediated blocking of free carboxylic acids (Asp/Glu sidechains and C-termini) with ethanolamine; reaction yields an amide-bond between the carboxylic acid of the peptide/protein and the primary amine of ethanolamine; reaction irreversibly modifies carboxylic acids. Shown above is the composition of the mass adduct, after substraction of water.
-xref: record_id "734"
-xref: delta_mono_mass "43.042199"
-xref: delta_avge_mass "43.0678"
-xref: delta_composition "H(5) C(2) N"
-xref: username_of_poster "overalllab"
-xref: group_of_poster ""
-xref: date_time_posted "2007-01-31 22:04:44"
-xref: date_time_modified "2012-11-01 12:02:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Any C-term"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "D"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "E"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "C"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:735
-name: BEMAD_ST
-def: "Beta elimination of modified S or T followed by Michael addition of DTT." [PMID:15648052, PMID:17116471, PMID:12438562, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=735]
-comment: Beta-elimination and Michael addition of dithiothreitol (DTT) to serine and threonine adds a weight of approximately 136.2.
-synonym: "threo-1,4-dimercaptobutane-2,3-diol Was DTT_ST" RELATED []
-xref: record_id "735"
-xref: delta_mono_mass "136.001656"
-xref: delta_avge_mass "136.2357"
-xref: delta_composition "H(8) C(4) O S(2)"
-xref: username_of_poster "stephenaw777"
-xref: group_of_poster ""
-xref: date_time_posted "2007-02-10 00:00:43"
-xref: date_time_modified "2017-06-15 14:01:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "The addition of DTT adds 136.2 not 154.2 to Serine due to loss of water in reaction"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_2_misc_notes "The addition of DTT adds 136.2 not 154.2 to Threonine due to loss of water in reaction"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:736
-name: BEMAD_C
-def: "Beta elimination of alkylated Cys followed by Michael addition of DTT." [PMID:12438562, PMID:17116471, PMID:16452088, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=736]
-comment: When the beta-elimination and Michael addition of dithiothreitol (DTT) (BEMAD) reaction is used with alkylated cysteine a sulfur group is lost leaving the addition of approximately 120.2 in the chemical reaction.
-synonym: "Was DTT_C" RELATED []
-xref: record_id "736"
-xref: delta_mono_mass "120.0245"
-xref: delta_avge_mass "120.1701"
-xref: delta_composition "H(8) C(4) O(2) S"
-xref: username_of_poster "stephenaw777"
-xref: group_of_poster ""
-xref: date_time_posted "2007-02-10 03:12:41"
-xref: date_time_modified "2017-06-15 13:58:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:737
-name: TMT6plex
-def: "Sixplex Tandem Mass Tag®." [URL:http\://www.piercenet.com/instructions/2162457.pdf, URL:https\://www.piercenet.com/instructions/2162073.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=737]
-comment: M/z values of the TMT® fragment ions to be quantified for 6plex and 10plex: 126.12773 127.12476 128.13443 129.13147 130.14114 131.13818. Additional m/z values for 10plex: 127.13108 128.12811 129.13779 130.13482.
-synonym: "Tandem Mass Tag sixplex labelling kit Proteome Sciences Also applies to TMT10plex Tandem Mass Tag® and TMT® are registered Trademarks of Proteome Sciences plc. This is a nominal. representative mass" RELATED []
-xref: record_id "737"
-xref: delta_mono_mass "229.162932"
-xref: delta_avge_mass "229.2634"
-xref: delta_composition "H(20) C(8) 13C(4) N 15N O(2)"
-xref: username_of_poster "JUergen.schaefer"
-xref: group_of_poster ""
-xref: date_time_posted "2007-03-01 13:44:23"
-xref: date_time_modified "2024-08-12 10:10:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Isotopic label"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "H"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "S"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Isotopic label"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "T"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:738
-name: TMT2plex
-def: "Duplex Tandem Mass Tag®." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=738]
-comment: Duplex-TMT® reagents 2TMT-126, 2TMT-127. m/z values of the TMT® fragment ions to be quantified: 126.12773 127.13108.
-synonym: "Tandem Mass Tag Duplex labelling kit Proteome Sciences Tandem Mass Tag® and TMT® are registered Trademarks of Proteome Sciences plc." RELATED []
-xref: record_id "738"
-xref: delta_mono_mass "225.155833"
-xref: delta_avge_mass "225.2921"
-xref: delta_composition "H(20) C(11) 13C N(2) O(2)"
-xref: username_of_poster "JUergen.schaefer"
-xref: group_of_poster ""
-xref: date_time_posted "2007-03-01 13:53:36"
-xref: date_time_modified "2024-08-12 10:09:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Isotopic label"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "H"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "S"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Isotopic label"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "T"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:739
-name: TMT
-def: "Native Tandem Mass Tag®." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=739]
-comment: This modification describes the \"native\" TMT Reagent without isotopic label.
-synonym: "Tandem Mass Tag® and TMT® are registered Trademarks of Proteome Sciences plc." RELATED []
-xref: record_id "739"
-xref: delta_mono_mass "224.152478"
-xref: delta_avge_mass "224.2994"
-xref: delta_composition "H(20) C(12) N(2) O(2)"
-xref: username_of_poster "JUergen.schaefer"
-xref: group_of_poster ""
-xref: date_time_posted "2007-03-02 09:29:50"
-xref: date_time_modified "2024-08-12 10:08:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "H"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "S"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Isotopic label"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "T"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:740
-name: ExacTagThiol
-def: "ExacTag Thiol label mass for 2-4-7-10 plex." [URL:http\://www.perkinelmer.com/exactag, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=740]
-comment: Accurate mass for Exactag Thiol labels.
-synonym: "PerkinElmer ExacTag Thiol kit" RELATED []
-xref: record_id "740"
-xref: delta_mono_mass "972.365219"
-xref: delta_avge_mass "972.7268"
-xref: delta_composition "H(50) C(23) 13C(12) N(8) 15N(6) O(18)"
-xref: username_of_poster "cparman"
-xref: group_of_poster ""
-xref: date_time_posted "2007-03-02 17:24:48"
-xref: date_time_modified "2017-10-09 15:48:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:741
-name: ExacTagAmine
-def: "ExacTag Amine label mass for 2-4-7-10 plex." [URL:http\://www.perkinelmer.com/exactag, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=741]
-comment: Accurate mass for Exactag Amine labels. Includes the mass of the conjugation reagent.
-synonym: "PerkinElmer ExacTag Amine kit" RELATED []
-xref: record_id "741"
-xref: delta_mono_mass "1046.347854"
-xref: delta_avge_mass "1046.8285"
-xref: delta_composition "H(52) C(25) 13C(12) N(8) 15N(6) O(19) S"
-xref: username_of_poster "cparman"
-xref: group_of_poster ""
-xref: date_time_posted "2007-03-02 17:28:02"
-xref: date_time_modified "2017-10-09 15:48:14"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:743
-name: 4-ONE+Delta:H(-2)O(-1)
-def: "Dehydrated 4-Oxononenal Michael adduct." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=743]
-comment: Mass Spectorscopic Characterization of Protein Modification by 4-hydroxy-2-(E)-nonenal and 4-oxo-2-(E)-nonenal.
-xref: record_id "743"
-xref: delta_mono_mass "136.088815"
-xref: delta_avge_mass "136.191"
-xref: delta_composition "H(12) C(9) O"
-xref: username_of_poster "stewartb"
-xref: group_of_poster ""
-xref: date_time_posted "2007-03-21 21:21:34"
-xref: date_time_modified "2007-04-08 18:56:36"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:744
-name: NO_SMX_SEMD
-def: "Nitroso Sulfamethoxazole Sulphenamide thiol adduct." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=744]
-comment: Synthesis and Reactions of Nitroso Sulphamethoxazole with Biological Nucleophiles: Implications for Immune Mediated Toxicity.
-xref: record_id "744"
-xref: delta_mono_mass "251.036462"
-xref: delta_avge_mass "251.2618"
-xref: delta_composition "H(9) C(10) N(3) O(3) S"
-xref: username_of_poster "stewartb"
-xref: group_of_poster ""
-xref: date_time_posted "2007-04-17 23:28:29"
-xref: date_time_modified "2021-07-06 12:30:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:746
-name: NO_SMX_SIMD
-def: "Nitroso Sulfamethoxazole Sulfinamide thiol adduct." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=746]
-comment: Synthesis and Reactions of Nitroso Sulphamethoxazole with Biological Nucleophiles: Implications for Immune Mediated Toxicity.
-xref: record_id "746"
-xref: delta_mono_mass "267.031377"
-xref: delta_avge_mass "267.2612"
-xref: delta_composition "H(9) C(10) N(3) O(4) S"
-xref: username_of_poster "stewartb"
-xref: group_of_poster ""
-xref: date_time_posted "2007-04-18 21:39:11"
-xref: date_time_modified "2007-04-21 16:56:07"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:747
-name: Malonyl
-def: "Malonylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=747]
-xref: record_id "747"
-xref: delta_mono_mass "86.000394"
-xref: delta_avge_mass "86.0462"
-xref: delta_composition "H(2) C(3) O(3)"
-xref: username_of_poster "massy"
-xref: group_of_poster ""
-xref: date_time_posted "2007-05-17 14:17:42"
-xref: date_time_modified "2024-06-27 10:17:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-xref: spec_3_neutral_loss_44_mono_mass "43.989829"
-xref: spec_3_neutral_loss_44_avge_mass "44.0095"
-xref: spec_3_neutral_loss_44_flag "false"
-xref: spec_3_neutral_loss_44_composition "C O(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:748
-name: 3sulfo
-def: "Derivatization by N-term modification using 3-Sulfobenzoic succinimidyl ester." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=748]
-xref: record_id "748"
-xref: delta_mono_mass "183.983029"
-xref: delta_avge_mass "184.1693"
-xref: delta_composition "H(4) C(7) O(4) S"
-xref: username_of_poster "MaxWis"
-xref: group_of_poster ""
-xref: date_time_posted "2007-05-31 10:15:48"
-xref: date_time_modified "2007-06-24 19:58:07"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:750
-name: trifluoro
-def: "Trifluoroleucine replacement of leucine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=750]
-xref: record_id "750"
-xref: delta_mono_mass "53.971735"
-xref: delta_avge_mass "53.9714"
-xref: delta_composition "H(-3) F(3)"
-xref: username_of_poster "UKMSF"
-xref: group_of_poster ""
-xref: date_time_posted "2007-06-13 17:10:33"
-xref: date_time_modified "2007-06-24 19:56:32"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Non-standard residue"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:751
-name: TNBS
-def: "Tri nitro benzene." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=751]
-xref: record_id "751"
-xref: delta_mono_mass "210.986535"
-xref: delta_avge_mass "211.0886"
-xref: delta_composition "H C(6) N(3) O(6)"
-xref: username_of_poster "DelphineP"
-xref: group_of_poster ""
-xref: date_time_posted "2007-06-21 13:36:03"
-xref: date_time_modified "2007-06-24 19:58:58"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:762
-name: IDEnT
-def: "Isotope Distribution Encoded Tag." [PMID:10740847, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=762]
-comment: Modified peptides identified by isotope pattern. Restriction to cysteine-containing peptides combined with high mass accuracy allows peptide identification.
-synonym: "2,4-dichlorobenzylcarbamidomethyl" RELATED []
-xref: record_id "762"
-xref: delta_mono_mass "214.990469"
-xref: delta_avge_mass "216.064"
-xref: delta_composition "H(7) C(9) N O Cl(2)"
-xref: username_of_poster "chalkley"
-xref: group_of_poster ""
-xref: date_time_posted "2007-07-10 20:14:50"
-xref: date_time_modified "2007-07-15 20:04:29"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:763
-name: BEMAD_ST:2H(6)
-def: "Beta elimination of modified S or T followed by Michael addition of labelled DTT." [PMID:15648052, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=763]
-comment: Can be used for quantitative analysis of O-linked post-translational modifications. Same reaction can be used for quantitative analysis of cysteine-containing peptides, but then the modification is 16 Da less in mass; i.e. isotopically labeled reagent adds 126 Da in mass.
-synonym: "Was DTT_ST:2H(6)" RELATED []
-xref: record_id "763"
-xref: delta_mono_mass "142.039317"
-xref: delta_avge_mass "142.2727"
-xref: delta_composition "H(2) 2H(6) C(4) O S(2)"
-xref: username_of_poster "chalkley"
-xref: group_of_poster ""
-xref: date_time_posted "2007-07-10 20:34:46"
-xref: date_time_modified "2017-06-15 14:01:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:764
-name: BEMAD_C:2H(6)
-def: "Beta elimination of alkylated Cys followed by Michael addition of labelled DTT." [PMID:15648052, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=764]
-comment: Can be used for quantitative analysis of cysteine-containing peptides. Same reaction can be used for quantitative analysis of O-linked post-translational modifications to serines and threonines, but then the modification is 16 Da more in mass; i.e. isotopically labeled reagent adds 142 Da in mass.
-synonym: "Was DTT_C:2H(6) Isotopically labeled Dithiothreitol (DTT) modification of cysteines" RELATED []
-xref: record_id "764"
-xref: delta_mono_mass "126.062161"
-xref: delta_avge_mass "126.2071"
-xref: delta_composition "H(2) 2H(6) C(4) O(2) S"
-xref: username_of_poster "chalkley"
-xref: group_of_poster ""
-xref: date_time_posted "2007-07-10 20:44:56"
-xref: date_time_modified "2017-06-15 13:59:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:765
-name: Met-loss
-def: "Removal of initiator methionine from protein N-terminus." [PMID:3327521, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=765]
-comment: N-terminal initiator methionine is removed by a methionine aminopeptidase from proteins where the residue following the methionine is Ala, Cys, Gly, Pro, Ser, Thr or Val. This is generally the final N-terminal state for proteins where the following residue was a Cys, Pro or Val.
-xref: record_id "765"
-xref: delta_mono_mass "-131.040485"
-xref: delta_avge_mass "-131.1961"
-xref: delta_composition "H(-9) C(-5) N(-1) O(-1) S(-1)"
-xref: username_of_poster "chalkley"
-xref: group_of_poster ""
-xref: date_time_posted "2007-07-10 22:40:00"
-xref: date_time_modified "2007-07-15 20:01:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Protein N-term"
-xref: spec_1_classification "Co-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:766
-name: Met-loss+Acetyl
-def: "Removal of initiator methionine from protein N-terminus, then acetylation of the new N-terminus." [PMID:3327521, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=766]
-comment: The N-terminal initiator methionine is removed by a methionine aminopeptidase from proteins whose residue following the methionine is Ala, Cys, Gly, Pro, Ser, Thr or Val. Proteins whose following residue was Ala, Gly, Ser or Thr are then acetylated by an N(alpha)-acetyltransferase on the new N-terminus.
-xref: record_id "766"
-xref: delta_mono_mass "-89.02992"
-xref: delta_avge_mass "-89.1594"
-xref: delta_composition "H(-7) C(-3) N(-1) S(-1)"
-xref: username_of_poster "chalkley"
-xref: group_of_poster ""
-xref: date_time_posted "2007-07-10 22:57:12"
-xref: date_time_modified "2007-07-15 20:01:06"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Protein N-term"
-xref: spec_1_classification "Co-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:767
-name: Menadione-HQ
-def: "Menadione hydroquinone derivative." [PMID:15939799, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=767]
-xref: record_id "767"
-xref: delta_mono_mass "172.05243"
-xref: delta_avge_mass "172.18"
-xref: delta_composition "H(8) C(11) O(2)"
-xref: username_of_poster "catsriku"
-xref: group_of_poster ""
-xref: date_time_posted "2007-07-12 07:35:07"
-xref: date_time_modified "2007-07-15 20:05:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:768
-name: Methyl+Acetyl:2H(3)
-def: "Mono-methylated lysine labelled with Acetyl_heavy." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=768]
-xref: record_id "768"
-xref: delta_mono_mass "59.045045"
-xref: delta_avge_mass "59.0817"
-xref: delta_composition "H 2H(3) C(3) O"
-xref: username_of_poster "buchanan"
-xref: group_of_poster ""
-xref: date_time_posted "2007-08-06 09:35:40"
-xref: date_time_modified "2007-09-07 16:56:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:771
-name: lapachenole
-def: "Lapachenole photochemically added to cysteine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=771]
-xref: record_id "771"
-xref: delta_mono_mass "240.11503"
-xref: delta_avge_mass "240.297"
-xref: delta_composition "H(16) C(16) O(2)"
-xref: username_of_poster "hmfales"
-xref: group_of_poster ""
-xref: date_time_posted "2007-08-17 22:22:15"
-xref: date_time_modified "2007-09-07 16:52:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "Simple cyclic compound C16H16O2 adds to cysteine forming fluorescent derivative."
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:772
-name: Label:13C(5)
-def: "13C(5) Silac label." [URL:http\://www.pil.sdu.dk/silac_intro.htm, PMID:12716131, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=772]
-xref: record_id "772"
-xref: delta_mono_mass "5.016774"
-xref: delta_avge_mass "4.9633"
-xref: delta_composition "C(-5) 13C(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2007-08-22 18:36:11"
-xref: date_time_modified "2007-08-22 18:36:11"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "Result of Arg to Pro conversion of 13C(6) labelled Arg"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:773
-name: maleimide
-def: "Maleimide." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=773]
-xref: record_id "773"
-xref: delta_mono_mass "97.016378"
-xref: delta_avge_mass "97.0721"
-xref: delta_composition "H(3) C(4) N O(2)"
-xref: username_of_poster "mjayson"
-xref: group_of_poster ""
-xref: date_time_posted "2007-09-05 23:31:52"
-xref: date_time_modified "2007-09-06 11:28:09"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:774
-name: Biotin-phenacyl
-def: "Alkylation by biotinylated form of phenacyl bromide." [PMID:428399, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=774]
-comment: Phenacyl bromide conjugated with a linker and biotin tag, details not published yet.
-xref: record_id "774"
-xref: delta_mono_mass "626.263502"
-xref: delta_avge_mass "626.727"
-xref: delta_composition "H(38) C(29) N(8) O(6) S"
-xref: username_of_poster "Sandeep"
-xref: group_of_poster ""
-xref: date_time_posted "2007-09-14 23:07:12"
-xref: date_time_modified "2007-10-03 15:42:46"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "S"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:775
-name: Carboxymethyl:13C(2)
-def: "Iodoacetic acid derivative w/ 13C label." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=775]
-synonym: "Carboxymethylation w/ 13C label" RELATED []
-xref: record_id "775"
-xref: delta_mono_mass "60.012189"
-xref: delta_avge_mass "60.0214"
-xref: delta_composition "H(2) 13C(2) O(2)"
-xref: username_of_poster "mpcusack"
-xref: group_of_poster ""
-xref: date_time_posted "2007-09-18 19:26:42"
-xref: date_time_modified "2008-06-22 12:00:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:776
-name: NEM:2H(5)
-def: "D5 N-ethylmaleimide on cysteines." [URL:http\://www.chemistry.ucsc.edu/~fink/231/Image118.gif, PMID:12777388, PMID:11813307, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=776]
-synonym: "CysNEM D5" RELATED []
-xref: record_id "776"
-xref: delta_mono_mass "130.079062"
-xref: delta_avge_mass "130.1561"
-xref: delta_composition "H(2) 2H(5) C(6) N O(2)"
-xref: username_of_poster "mpcusack"
-xref: group_of_poster ""
-xref: date_time_posted "2007-09-18 19:49:39"
-xref: date_time_modified "2007-09-28 10:37:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:792
-name: AEC-MAEC:2H(4)
-def: "Deuterium cysteamine modification to S or T." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=792]
-xref: record_id "792"
-xref: delta_mono_mass "63.044462"
-xref: delta_avge_mass "63.158"
-xref: delta_composition "H 2H(4) C(2) N O(-1) S"
-xref: username_of_poster "zwang23"
-xref: group_of_poster ""
-xref: date_time_posted "2007-10-03 19:41:19"
-xref: date_time_modified "2007-10-08 13:44:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:793
-name: Hex(1)HexNAc(1)
-def: "Hex1HexNAc1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=793]
-xref: record_id "793"
-xref: delta_mono_mass "365.132196"
-xref: delta_avge_mass "365.3331"
-xref: delta_composition "Hex HexNAc"
-xref: username_of_poster "julienjardin"
-xref: group_of_poster ""
-xref: date_time_posted "2007-10-12 13:16:23"
-xref: date_time_modified "2017-11-23 13:04:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_366_mono_mass "365.132196"
-xref: spec_1_neutral_loss_366_avge_mass "365.3331"
-xref: spec_1_neutral_loss_366_flag "false"
-xref: spec_1_neutral_loss_366_composition "Hex HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_366_mono_mass "365.132196"
-xref: spec_1_neutral_loss_366_avge_mass "365.3331"
-xref: spec_1_neutral_loss_366_flag "false"
-xref: spec_1_neutral_loss_366_composition "Hex HexNAc"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_misc_notes "Not reported for human proteins"
-xref: spec_2_neutral_loss_366_mono_mass "365.132196"
-xref: spec_2_neutral_loss_366_avge_mass "365.3331"
-xref: spec_2_neutral_loss_366_flag "false"
-xref: spec_2_neutral_loss_366_composition "Hex HexNAc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:799
-name: Label:13C(6)+GG
-def: "13C6 labeled ubiquitinylation residue." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=799]
-comment: The two glycine residues left on SILAC labeled ubiquitinylated lysine after tryptic digestion.
-xref: record_id "799"
-xref: delta_mono_mass "120.063056"
-xref: delta_avge_mass "120.0586"
-xref: delta_composition "H(6) C(-2) 13C(6) N(2) O(2)"
-xref: username_of_poster "glick2"
-xref: group_of_poster ""
-xref: date_time_posted "2007-12-02 22:45:39"
-xref: date_time_modified "2014-07-09 16:53:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:800
-name: Biotin:Thermo-21345
-def: "Was PentylamineBiotin." [URL:http\://www.piercenet.com/Products/Browse.cfm?fldID=01031206, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=800]
-synonym: "Used for labeling glutamine-donor substrate of transglutaminase" RELATED []
-xref: record_id "800"
-xref: delta_mono_mass "311.166748"
-xref: delta_avge_mass "311.4429"
-xref: delta_composition "H(25) C(15) N(3) O(2) S"
-xref: username_of_poster "mengyi"
-xref: group_of_poster ""
-xref: date_time_posted "2007-12-03 13:56:58"
-xref: date_time_modified "2015-01-21 09:40:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:801
-name: Pentylamine
-def: "Labeling transglutaminase substrate on glutamine side chain." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=801]
-xref: record_id "801"
-xref: delta_mono_mass "70.07825"
-xref: delta_avge_mass "70.1329"
-xref: delta_composition "H(10) C(5)"
-xref: username_of_poster "mengyi"
-xref: group_of_poster ""
-xref: date_time_posted "2007-12-05 11:08:02"
-xref: date_time_modified "2021-07-20 13:24:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:811
-name: Biotin:Thermo-21360
-def: "Was Biotin-PEO4-hydrazide." [URL:http\://www.piercenet.com/products/browse.cfm?fldID=C4FE82D4-DD06-493C-8EC4-9C1D7F83211B, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=811]
-synonym: "Pierce EZ link biotin hydrazide prod no. 21360" RELATED []
-xref: record_id "811"
-xref: delta_mono_mass "487.246455"
-xref: delta_avge_mass "487.6134"
-xref: delta_composition "H(37) C(21) N(5) O(6) S"
-xref: username_of_poster "MCole18"
-xref: group_of_poster ""
-xref: date_time_posted "2007-12-12 15:23:23"
-xref: date_time_modified "2010-12-03 16:05:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "hydrazide reacts at any activated carboxyl group"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:821
-name: Cy3b-maleimide
-def: "Fluorescent dye that labels cysteines." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=821]
-synonym: "Cy3b meleimide reacted with Cysteine Formula requires confirmation" RELATED []
-xref: record_id "821"
-xref: delta_mono_mass "682.24612"
-xref: delta_avge_mass "682.7852"
-xref: delta_composition "H(38) C(37) N(4) O(7) S"
-xref: username_of_poster "kfinan"
-xref: group_of_poster ""
-xref: date_time_posted "2008-02-01 16:03:09"
-xref: date_time_modified "2012-09-14 23:51:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:822
-name: Gly-loss+Amide
-def: "Enzymatic glycine removal leaving an amidated C-terminus." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=822]
-synonym: "Amidation requires presence of glycine at peptide terminus" RELATED []
-xref: record_id "822"
-xref: delta_mono_mass "-58.005479"
-xref: delta_avge_mass "-58.0361"
-xref: delta_composition "H(-2) C(-2) O(-2)"
-xref: username_of_poster "timothyr"
-xref: group_of_poster ""
-xref: date_time_posted "2008-02-06 09:33:39"
-xref: date_time_modified "2010-07-14 23:15:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Any C-term"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:824
-name: Xlink:BMOE
-def: "Intact or monolink BMOE crosslinker." [URL:http\://tools.thermofisher.com/content/sfs/manuals/MAN0011308_Bismaleimide_CrsLnk_BMOE_BMB_BMH_UG.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=824]
-xref: record_id "824"
-xref: delta_mono_mass "220.048407"
-xref: delta_avge_mass "220.1815"
-xref: delta_composition "H(8) C(10) N(2) O(4)"
-xref: username_of_poster "Larsenmarsen"
-xref: group_of_poster ""
-xref: date_time_posted "2008-02-13 15:28:55"
-xref: date_time_modified "2017-08-18 11:12:14"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:825
-name: Xlink:DFDNB
-def: "Intact DFDNB crosslinker." [URL:http\://tools.thermofisher.com/content/sfs/manuals/MAN0011313_DFDNB_UG.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=825]
-xref: record_id "825"
-xref: delta_mono_mass "163.985807"
-xref: delta_avge_mass "164.0752"
-xref: delta_composition "C(6) N(2) O(4)"
-xref: username_of_poster "Larsenmarsen"
-xref: group_of_poster ""
-xref: date_time_posted "2008-02-13 15:35:40"
-xref: date_time_modified "2017-08-18 11:55:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "R"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Q"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "N"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:827
-name: TMPP-Ac
-def: "Tris(2,4,6-trimethoxyphenyl)phosphonium acetic acid N-hydroxysuccinimide ester derivative." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=827]
-comment: The formula has been reduced from H(34) to H(33) on 13 May 2009 so as to give correct observed m/z values. The charge on the TMPP means that ions have one less proton than would be expected.
-xref: record_id "827"
-xref: delta_mono_mass "572.181134"
-xref: delta_avge_mass "572.5401"
-xref: delta_composition "H(33) C(29) O(10) P"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2008-02-20 14:12:31"
-xref: date_time_modified "2018-06-26 15:22:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:830
-name: Dihydroxyimidazolidine
-def: "Dihydroxy methylglyoxal adduct." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=830]
-xref: record_id "830"
-xref: delta_mono_mass "72.021129"
-xref: delta_avge_mass "72.0627"
-xref: delta_composition "H(4) C(3) O(2)"
-xref: username_of_poster "kimzey"
-xref: group_of_poster ""
-xref: date_time_posted "2008-03-04 00:00:29"
-xref: date_time_modified "2008-05-22 00:32:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Multiple"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:834
-name: Label:2H(4)+Acetyl
-def: "Acetyl 4,4,5,5-D4 Lysine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=834]
-comment: For SILAC experiments, + PTM.
-synonym: "Acetyl_K4" RELATED []
-xref: record_id "834"
-xref: delta_mono_mass "46.035672"
-xref: delta_avge_mass "46.0613"
-xref: delta_composition "H(-2) 2H(4) C(2) O"
-xref: username_of_poster "Raghothama"
-xref: group_of_poster ""
-xref: date_time_posted "2008-03-24 17:25:15"
-xref: date_time_modified "2008-04-02 10:17:08"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "Both isotopiclabel and post translational mod"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:835
-name: Label:13C(6)+Acetyl
-def: "Acetyl 13C(6) Silac label." [URL:http\://www.pil.sdu.dk/silac_intro.htm, PMID:12716131, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=835]
-xref: record_id "835"
-xref: delta_mono_mass "48.030694"
-xref: delta_avge_mass "47.9926"
-xref: delta_composition "H(2) C(-4) 13C(6) O"
-xref: username_of_poster "Raghothama"
-xref: group_of_poster ""
-xref: date_time_posted "2008-03-24 17:33:44"
-xref: date_time_modified "2008-04-02 10:14:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "SILAC and PTM"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:836
-name: Label:13C(6)15N(2)+Acetyl
-def: "Acetyl_13C(6) 15N(2) Silac label." [URL:http\://www.pil.sdu.dk/silac_intro.htm, PMID:12716131, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=836]
-synonym: "Acetyl_heavy lysine" RELATED []
-xref: record_id "836"
-xref: delta_mono_mass "50.024764"
-xref: delta_avge_mass "49.9794"
-xref: delta_composition "H(2) C(-4) 13C(6) N(-2) 15N(2) O"
-xref: username_of_poster "Raghothama"
-xref: group_of_poster ""
-xref: date_time_posted "2008-03-24 17:35:52"
-xref: date_time_modified "2008-04-02 10:13:59"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "Used in SILAC experiment"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:837
-name: Arg->Npo
-def: "Arginine replacement by Nitropyrimidyl ornithine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=837]
-xref: record_id "837"
-xref: delta_mono_mass "80.985078"
-xref: delta_avge_mass "81.0297"
-xref: delta_composition "H(-1) C(3) N O(2)"
-xref: username_of_poster "Kramerh"
-xref: group_of_poster ""
-xref: date_time_posted "2008-04-10 15:35:22"
-xref: date_time_modified "2008-04-21 18:30:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:846
-name: EQIGG
-def: "Sumo mutant Smt3-WT tail following trypsin digestion." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=846]
-synonym: "Sumoylation" RELATED []
-xref: record_id "846"
-xref: delta_mono_mass "484.228162"
-xref: delta_avge_mass "484.5035"
-xref: delta_composition "H(32) C(20) N(6) O(8)"
-xref: username_of_poster "Magnojunqueira"
-xref: group_of_poster ""
-xref: date_time_posted "2008-05-13 16:56:23"
-xref: date_time_modified "2008-05-17 18:58:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:848
-name: Arg2PG
-def: "Adduct of phenylglyoxal with Arg." [PMID:11945751, PMID:11698400, PMID:5723461, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=848]
-xref: record_id "848"
-xref: delta_mono_mass "266.057909"
-xref: delta_avge_mass "266.2482"
-xref: delta_composition "H(10) C(16) O(4)"
-xref: username_of_poster "Kramerh"
-xref: group_of_poster ""
-xref: date_time_posted "2008-05-16 11:07:51"
-xref: date_time_modified "2008-11-21 18:13:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "The reaction product of Arg with phenylglyoxal has been shown to be a 2:1 adduct"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:849
-name: cGMP
-def: "S-guanylation." [PMID:17906641, PMID:15063129, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=849]
-comment: Protein which is posttranslationally modified by the attachment of cGMP on the sulfur atom of Cys or hydroxyl group of Ser residues.
-xref: record_id "849"
-xref: delta_mono_mass "343.031785"
-xref: delta_avge_mass "343.1895"
-xref: delta_composition "H(10) C(10) N(5) O(7) P"
-xref: username_of_poster "atsushiirie"
-xref: group_of_poster ""
-xref: date_time_posted "2008-06-21 09:02:53"
-xref: date_time_modified "2014-02-08 02:24:10"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:851
-name: cGMP+RMP-loss
-def: "S-guanylation-2." [PMID:17906641, PMID:15063129, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=851]
-comment: Protein which is posttranslationally modified by the attachment of cGMP that has lost ribose 3\',5\'-cyclic monophosphate moiety on the sulfur atom of Cys or hydroxyl group of Ser.
-xref: record_id "851"
-xref: delta_mono_mass "150.041585"
-xref: delta_avge_mass "150.1182"
-xref: delta_composition "H(4) C(5) N(5) O"
-xref: username_of_poster "atsushiirie"
-xref: group_of_poster ""
-xref: date_time_posted "2008-06-21 09:06:56"
-xref: date_time_modified "2009-05-24 20:03:08"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:853
-name: Label:2H(4)+GG
-def: "Ubiquitination 2H4 lysine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=853]
-xref: record_id "853"
-xref: delta_mono_mass "118.068034"
-xref: delta_avge_mass "118.1273"
-xref: delta_composition "H(2) 2H(4) C(4) N(2) O(2)"
-xref: username_of_poster "Raghothama"
-xref: group_of_poster ""
-xref: date_time_posted "2008-06-27 14:28:36"
-xref: date_time_modified "2014-07-09 16:52:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:859
-name: MG-H1
-def: "Methylglyoxal-derived hydroimidazolone." [PMID:15377717, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=859]
-xref: record_id "859"
-xref: delta_mono_mass "54.010565"
-xref: delta_avge_mass "54.0474"
-xref: delta_composition "H(2) C(3) O"
-xref: username_of_poster "AndrewW"
-xref: group_of_poster ""
-xref: date_time_posted "2008-07-24 14:41:07"
-xref: date_time_modified "2008-07-31 17:14:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:860
-name: G-H1
-def: "Glyoxal-derived hydroimiadazolone." [PMID:17143934, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=860]
-xref: record_id "860"
-xref: delta_mono_mass "39.994915"
-xref: delta_avge_mass "40.0208"
-xref: delta_composition "C(2) O"
-xref: username_of_poster "AndrewW"
-xref: group_of_poster ""
-xref: date_time_posted "2008-07-24 14:44:11"
-xref: date_time_modified "2008-07-31 17:16:39"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:861
-name: ZGB
-def: "NHS ester linked Green Fluorescent Bodipy Dye." [URL:http\://www.zdye.com/, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=861]
-xref: record_id "861"
-xref: delta_mono_mass "758.380841"
-xref: delta_avge_mass "758.7261"
-xref: delta_composition "H(53) B C(37) N(6) O(6) F(2) S"
-xref: username_of_poster "JBowden"
-xref: group_of_poster ""
-xref: date_time_posted "2008-07-30 14:51:06"
-xref: date_time_modified "2008-09-22 21:42:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:862
-name: Label:13C(1)2H(3)
-def: "SILAC." [URL:http\://www.pil.sdu.dk/silac_intro.htm, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=862]
-xref: record_id "862"
-xref: delta_mono_mass "4.022185"
-xref: delta_avge_mass "4.0111"
-xref: delta_composition "H(-3) 2H(3) C(-1) 13C"
-xref: username_of_poster "msalek"
-xref: group_of_poster ""
-xref: date_time_posted "2008-08-11 13:43:25"
-xref: date_time_modified "2008-08-14 18:16:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "Isotopic labeled methionine SILAC"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:864
-name: Label:13C(6)15N(2)+GG
-def: "13C(6) 15N(2) Lysine glygly." [PMID:12716131, URL:http\://www.pil.sdu.dk/silac_intro.htm, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=864]
-synonym: "heavy glygly lysine" RELATED []
-xref: record_id "864"
-xref: delta_mono_mass "122.057126"
-xref: delta_avge_mass "122.0454"
-xref: delta_composition "H(6) C(-2) 13C(6) 15N(2) O(2)"
-xref: username_of_poster "Raghothama"
-xref: group_of_poster ""
-xref: date_time_posted "2008-08-13 21:56:52"
-xref: date_time_modified "2014-07-09 16:53:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "Used in SILAC PTM (glygly) experiment"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:866
-name: ICPL:13C(6)2H(4)
-def: "Bruker Daltonics SERVA-ICPL(TM) quantification chemistry, +10 Da form." [URL:http\://www.bdal.de/life-science-tools/care-consumables-more/icpl-kit.html, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=866]
-comment: Attention: As the digest is typically applied AFTER ICPL labeling, only ProteinN-term labeling and Lys-specific labeling is applied.
-synonym: "ICPL_10" RELATED []
-xref: record_id "866"
-xref: delta_mono_mass "115.0667"
-xref: delta_avge_mass "115.0747"
-xref: delta_composition "H(-1) 2H(4) 13C(6) N O"
-xref: username_of_poster "suckau"
-xref: group_of_poster ""
-xref: date_time_posted "2008-09-03 15:17:21"
-xref: date_time_modified "2008-09-12 11:59:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_2_misc_notes "Use when labelling pre-digest"
-xref: spec_3_group "3"
-xref: spec_3_hidden "0"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Use when labelling post-digest"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:876
-name: QEQTGG
-def: "SUMOylation by SUMO-1." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=876]
-synonym: "GlnGluGlnThrGlyGly" RELATED []
-xref: record_id "876"
-xref: delta_mono_mass "600.250354"
-xref: delta_avge_mass "600.5789"
-xref: delta_composition "H(36) C(23) N(8) O(11)"
-xref: username_of_poster "oosula"
-xref: group_of_poster ""
-xref: date_time_posted "2008-09-09 17:02:45"
-xref: date_time_modified "2011-11-25 13:05:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_1_misc_notes "This peptide is generated from a trypsin/chymotrypsin dual digest."
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:877
-name: QQQTGG
-def: "SUMOylation by SUMO-2/3." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=877]
-synonym: "GlnGlnGlnThrGlyGly" RELATED []
-xref: record_id "877"
-xref: delta_mono_mass "599.266339"
-xref: delta_avge_mass "599.5942"
-xref: delta_composition "H(37) C(23) N(9) O(10)"
-xref: username_of_poster "oosula"
-xref: group_of_poster ""
-xref: date_time_posted "2008-09-09 17:09:04"
-xref: date_time_modified "2008-09-19 19:06:46"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_1_misc_notes "This peptide is generated from a trypsin/chymotrypsin dual digest"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:884
-name: Biotin:Thermo-21325
-def: "Was ChromoBiotin." [URL:http\://www.piercenet.com/Products/Browse.cfm?fldID=44B1F9DF-B306-4278-B292-6CDB5B3B9D53, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=884]
-synonym: "EZ-Link NHS-Chromogenic Biotin" RELATED []
-xref: record_id "884"
-xref: delta_mono_mass "695.310118"
-xref: delta_avge_mass "695.8288"
-xref: delta_composition "H(45) C(34) N(7) O(7) S"
-xref: username_of_poster "chens002"
-xref: group_of_poster ""
-xref: date_time_posted "2008-10-20 13:26:20"
-xref: date_time_modified "2010-12-03 16:04:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:885
-name: Label:13C(1)2H(3)+Oxidation
-def: "Oxidised methionine 13C(1)2H(3) SILAC label." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=885]
-xref: record_id "885"
-xref: delta_mono_mass "20.0171"
-xref: delta_avge_mass "20.0105"
-xref: delta_composition "H(-3) 2H(3) C(-1) 13C O"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2008-10-24 09:47:20"
-xref: date_time_modified "2009-09-25 13:15:07"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Multiple"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:886
-name: HydroxymethylOP
-def: "2-ammonio-6-[4-(hydroxymethyl)-3-oxidopyridinium-1-yl]- hexanoate." [PMID:12595094, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=886]
-xref: record_id "886"
-xref: delta_mono_mass "108.021129"
-xref: delta_avge_mass "108.0948"
-xref: delta_composition "H(4) C(6) O(2)"
-xref: username_of_poster "AndrewW"
-xref: group_of_poster ""
-xref: date_time_posted "2008-11-03 14:35:36"
-xref: date_time_modified "2008-11-09 17:49:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_1_misc_notes "Advanced Glycation Endproduct"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:887
-name: MDCC
-def: "Covalent linkage of maleimidyl coumarin probe (Molecular Probes D-10253)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=887]
-comment: MDCC is used extensively as a fluorescent probe to report changes in protein conformation.
-synonym: "CAS 156571-46-9 7-diethylamino-3-((((2-maleimidyl)ethyl)amino)carbonyl)coumarin" RELATED []
-xref: record_id "887"
-xref: delta_mono_mass "383.148121"
-xref: delta_avge_mass "383.3978"
-xref: delta_composition "H(21) C(20) N(3) O(5)"
-xref: username_of_poster "shartson"
-xref: group_of_poster ""
-xref: date_time_posted "2008-12-03 16:20:46"
-xref: date_time_modified "2008-12-05 09:32:22"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "Due to the mechanism of maleimidyl modification of Cys, the molecular weight of MDCC equals the mass shift created upon crossllinking (no chemical leaving group). During MS/MS, MDCC can reasonably be predicted to fragment readily and at various positions."
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:888
-name: mTRAQ
-def: "MTRAQ light." [URL:http\://www3.appliedbiosystems.com/cms/groups/psm_support/documents/generaldocuments/cms_054141.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=888]
-synonym: "Applied Biosystems mTRAQ(TM) reagent" RELATED []
-xref: record_id "888"
-xref: delta_mono_mass "140.094963"
-xref: delta_avge_mass "140.183"
-xref: delta_composition "H(12) C(7) N(2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2008-12-04 13:50:02"
-xref: date_time_modified "2011-11-25 10:30:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "0"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Low abundance"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "H"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "Very low abundance"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "S"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Isotopic label"
-xref: spec_5_misc_notes "Very low abundance"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "T"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Isotopic label"
-xref: spec_6_misc_notes "Very low abundance"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:889
-name: mTRAQ:13C(3)15N(1)
-def: "MTRAQ medium." [URL:http\://www3.appliedbiosystems.com/cms/groups/psm_support/documents/generaldocuments/cms_054141.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=889]
-synonym: "mTRAQ medium is identical to iTRAQ4plex 117 Applied Biosystems mTRAQ(TM) reagent" RELATED []
-xref: record_id "889"
-xref: delta_mono_mass "144.102063"
-xref: delta_avge_mass "144.1544"
-xref: delta_composition "H(12) C(4) 13C(3) N 15N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2008-12-05 09:26:02"
-xref: date_time_modified "2011-11-25 10:34:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "0"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Low abundance"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "H"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "Very low abundance"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "S"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Isotopic label"
-xref: spec_5_misc_notes "Very low abundance"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "T"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Isotopic label"
-xref: spec_6_misc_notes "Very low abundance"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:890
-name: DyLight-maleimide
-def: "Thiol-reactive dye for fluorescence labelling of proteins." [URL:http\://www.piercenet.com/files/1964as4.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=890]
-xref: record_id "890"
-xref: delta_mono_mass "940.1999"
-xref: delta_avge_mass "941.0762"
-xref: delta_composition "H(48) C(39) N(4) O(15) S(4)"
-xref: username_of_poster "anikolakakis"
-xref: group_of_poster ""
-xref: date_time_posted "2008-12-05 15:23:15"
-xref: date_time_modified "2008-12-15 12:17:39"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:891
-name: Methyl-PEO12-Maleimide
-def: "Methyl-PEO12-Maleimide." [URL:http\://www.piercenet.com/files/1768dh5.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=891]
-xref: record_id "891"
-xref: delta_mono_mass "710.383719"
-xref: delta_avge_mass "710.8073"
-xref: delta_composition "H(58) C(32) N(2) O(15)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2008-12-09 11:02:18"
-xref: date_time_modified "2008-12-15 12:15:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:893
-name: CarbamidomethylDTT
-def: "Carbamidomethylated DTT modification of cysteine." [PMID:18653769, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=893]
-xref: record_id "893"
-xref: delta_mono_mass "209.018035"
-xref: delta_avge_mass "209.2864"
-xref: delta_composition "H(11) C(6) N O(3) S(2)"
-xref: username_of_poster "chalkley"
-xref: group_of_poster ""
-xref: date_time_posted "2009-01-09 01:39:37"
-xref: date_time_modified "2017-06-15 14:11:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:894
-name: CarboxymethylDTT
-def: "Carboxymethylated DTT modification of cysteine." [PMID:18653769, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=894]
-xref: record_id "894"
-xref: delta_mono_mass "210.00205"
-xref: delta_avge_mass "210.2712"
-xref: delta_composition "H(10) C(6) O(4) S(2)"
-xref: username_of_poster "chalkley"
-xref: group_of_poster ""
-xref: date_time_posted "2009-01-09 01:43:09"
-xref: date_time_modified "2009-01-10 19:03:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:895
-name: Biotin-PEG-PRA
-def: "Biotin polyethyleneoxide (n=3) alkyne." [URL:http\://etd.caltech.edu/etd/available/etd-09132005-120123/unrestricted/Chapter2.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=895]
-comment: Methionine (C5H11NO2S) is substituted in cell culture by Azidohomoalanine (C4H8N4O2). The azido group reacts with an alkyne group attached to a linker (PEO) with a biotin group at the end (C27H45N5O7S). As a result the side chain of Met (C3H7S) is substitued by C29H49N8O7S.
-xref: record_id "895"
-xref: delta_mono_mass "578.317646"
-xref: delta_avge_mass "578.6611"
-xref: delta_composition "H(42) C(26) N(8) O(7)"
-xref: username_of_poster "Larsenmarsen"
-xref: group_of_poster ""
-xref: date_time_posted "2009-01-19 10:54:58"
-xref: date_time_modified "2009-02-06 16:50:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:896
-name: Met->Aha
-def: "Methionine replacement by azido homoalanine." [PMID:16281315, PMID:11752401, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=896]
-xref: record_id "896"
-xref: delta_mono_mass "-4.986324"
-xref: delta_avge_mass "-5.0794"
-xref: delta_composition "H(-3) C(-1) N(3) S(-1)"
-xref: username_of_poster "Kramerh"
-xref: group_of_poster ""
-xref: date_time_posted "2009-01-30 14:52:20"
-xref: date_time_modified "2009-02-06 16:38:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Non-standard residue"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:897
-name: Label:15N(4)
-def: "SILAC 15N(4)." [URL:http\://www.pil.sdu.dk/silac_intro.htm, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=897]
-synonym: "Metabolic labeling with ammonium sulfate (15N)" RELATED []
-xref: record_id "897"
-xref: delta_mono_mass "3.98814"
-xref: delta_avge_mass "3.9736"
-xref: delta_composition "N(-4) 15N(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2009-02-06 15:29:55"
-xref: date_time_modified "2011-11-21 14:26:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:898
-name: pyrophospho
-def: "Pyrophosphorylation of Ser/Thr." [PMID:17873058, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=898]
-xref: record_id "898"
-xref: delta_mono_mass "159.932662"
-xref: delta_avge_mass "159.9598"
-xref: delta_composition "H(2) O(6) P(2)"
-xref: username_of_poster "Kramerh"
-xref: group_of_poster ""
-xref: date_time_posted "2009-02-23 20:54:00"
-xref: date_time_modified "2009-11-11 09:39:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_1_neutral_loss_177_mono_mass "176.935402"
-xref: spec_1_neutral_loss_177_avge_mass "176.9671"
-xref: spec_1_neutral_loss_177_flag "false"
-xref: spec_1_neutral_loss_177_composition "H(3) O(7) P(2)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_2_neutral_loss_177_mono_mass "176.935402"
-xref: spec_2_neutral_loss_177_avge_mass "176.9671"
-xref: spec_2_neutral_loss_177_flag "false"
-xref: spec_2_neutral_loss_177_composition "H(3) O(7) P(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:899
-name: Met->Hpg
-def: "Methionine replacement by homopropargylglycine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=899]
-xref: record_id "899"
-xref: delta_mono_mass "-21.987721"
-xref: delta_avge_mass "-22.0702"
-xref: delta_composition "H(-2) C S(-1)"
-xref: username_of_poster "Kramerh"
-xref: group_of_poster ""
-xref: date_time_posted "2009-02-24 17:11:44"
-xref: date_time_modified "2009-03-13 16:00:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Non-standard residue"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:901
-name: 4AcAllylGal
-def: "2,3,4,6-tetra-O-Acetyl-1-allyl-alpha-D-galactopyranoside modification of cysteine." [PMID:18275052, PMID:19798718, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=901]
-xref: record_id "901"
-xref: delta_mono_mass "372.142033"
-xref: delta_avge_mass "372.3671"
-xref: delta_composition "H(24) C(17) O(9)"
-xref: username_of_poster "paolo.nanni"
-xref: group_of_poster ""
-xref: date_time_posted "2009-03-06 16:08:43"
-xref: date_time_modified "2014-06-23 14:32:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:902
-name: DimethylArsino
-def: "Reaction with dimethylarsinous (AsIII) acid." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=902]
-comment: Protein from animals exposed to organoarsenicals.
-xref: record_id "902"
-xref: delta_mono_mass "103.960719"
-xref: delta_avge_mass "103.9827"
-xref: delta_composition "H(5) C(2) As"
-xref: username_of_poster "dashford"
-xref: group_of_poster ""
-xref: date_time_posted "2009-03-09 17:03:27"
-xref: date_time_modified "2009-03-13 15:59:22"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:903
-name: Lys->CamCys
-def: "Lys->Cys substitution and carbamidomethylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=903]
-comment: For Brad Strader.
-xref: record_id "903"
-xref: delta_mono_mass "31.935685"
-xref: delta_avge_mass "32.0219"
-xref: delta_composition "H(-4) C(-1) O S"
-xref: username_of_poster "hooverdm"
-xref: group_of_poster ""
-xref: date_time_posted "2009-04-17 14:47:30"
-xref: date_time_modified "2009-05-01 16:47:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Pre-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:904
-name: Phe->CamCys
-def: "Phe->Cys substitution and carbamidomethylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=904]
-comment: For Brad Strader.
-xref: record_id "904"
-xref: delta_mono_mass "12.962234"
-xref: delta_avge_mass "13.0204"
-xref: delta_composition "H(-1) C(-4) N O S"
-xref: username_of_poster "hooverdm"
-xref: group_of_poster ""
-xref: date_time_posted "2009-04-17 14:49:02"
-xref: date_time_modified "2009-07-13 18:16:29"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Pre-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:905
-name: Leu->MetOx
-def: "Leu->Met substitution and sulfoxidation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=905]
-comment: For Brad Strader.
-xref: record_id "905"
-xref: delta_mono_mass "33.951335"
-xref: delta_avge_mass "34.0378"
-xref: delta_composition "H(-2) C(-1) O S"
-xref: username_of_poster "hooverdm"
-xref: group_of_poster ""
-xref: date_time_posted "2009-04-17 14:50:35"
-xref: date_time_modified "2009-05-01 16:47:06"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Pre-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:906
-name: Lys->MetOx
-def: "Lys->Met substitution and sulfoxidation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=906]
-comment: For Brad Strader.
-xref: record_id "906"
-xref: delta_mono_mass "18.940436"
-xref: delta_avge_mass "19.0232"
-xref: delta_composition "H(-3) C(-1) N(-1) O S"
-xref: username_of_poster "hooverdm"
-xref: group_of_poster ""
-xref: date_time_posted "2009-04-17 14:51:35"
-xref: date_time_modified "2009-05-01 16:46:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Pre-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:907
-name: Galactosyl
-def: "Gluconoylation." [URL:http\://www.abrf.org/index.cfm/dm.details?DMID=226&AvgMass=all&Margin=0, PMID:743239, PMID:18083862, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=907]
-xref: record_id "907"
-xref: delta_mono_mass "178.047738"
-xref: delta_avge_mass "178.14"
-xref: delta_composition "O Hex"
-xref: username_of_poster "zientek"
-xref: group_of_poster ""
-xref: date_time_posted "2009-04-21 18:11:24"
-xref: date_time_modified "2015-05-07 11:02:58"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other glycosylation"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Other glycosylation"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:908
-name: Xlink:SMCC[321]
-def: "Monolink of SMCC terminated with 3-(dimethylamino)-1-propylamine." [URL:https\://assets.thermofisher.com/TFS-Assets/LSG/manuals/MAN0011295_SMCC_SulfoSMCC_UG.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=908]
-xref: record_id "908"
-xref: delta_mono_mass "321.205242"
-xref: delta_avge_mass "321.4146"
-xref: delta_composition "H(27) C(17) N(3) O(3)"
-xref: username_of_poster "anikolakakis"
-xref: group_of_poster ""
-xref: date_time_posted "2009-04-23 19:39:42"
-xref: date_time_modified "2017-09-01 14:46:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:910
-name: Bacillosamine
-def: "2,4-diacetamido-2,4,6-trideoxyglucopyranose." [PMID:12186869, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=910]
-synonym: "Asn-linked glycan from Gram-negative Bacterium DATDH" RELATED []
-xref: record_id "910"
-xref: delta_mono_mass "228.111007"
-xref: delta_avge_mass "228.245"
-xref: delta_composition "H(6) C(4) N(2) dHex"
-xref: username_of_poster "rlmoritz"
-xref: group_of_poster ""
-xref: date_time_posted "2009-06-23 18:27:32"
-xref: date_time_modified "2017-11-29 14:04:43"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_229_mono_mass "228.111007"
-xref: spec_1_neutral_loss_229_avge_mass "228.245"
-xref: spec_1_neutral_loss_229_flag "false"
-xref: spec_1_neutral_loss_229_composition "H(6) C(4) N(2) dHex"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:911
-name: MTSL
-def: "Cys modification by (1-oxyl-2,2,5,5-tetramethyl-3-pyrroline-3-methyl)methanesulfonate (MTSL)." [PMID:9335564, PMID:12441112, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=911]
-xref: record_id "911"
-xref: delta_mono_mass "184.07961"
-xref: delta_avge_mass "184.2786"
-xref: delta_composition "H(14) C(9) N O S"
-xref: username_of_poster "Kramerh"
-xref: group_of_poster ""
-xref: date_time_posted "2009-06-25 20:19:40"
-xref: date_time_modified "2009-06-26 11:13:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:912
-name: HNE-BAHAH
-def: "4-hydroxy-2-nonenal and biotinamidohexanoic acid hydrazide, reduced." [PMID:19054759, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=912]
-comment: For Bindu Abraham.
-xref: record_id "912"
-xref: delta_mono_mass "511.319226"
-xref: delta_avge_mass "511.7209"
-xref: delta_composition "H(45) C(25) N(5) O(4) S"
-xref: username_of_poster "hooverdm"
-xref: group_of_poster ""
-xref: date_time_posted "2009-07-13 18:23:28"
-xref: date_time_modified "2009-07-17 17:49:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:914
-name: Methylmalonylation
-def: "Methylmalonylation on Serine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=914]
-comment: Structural isomer to succinyl.
-xref: record_id "914"
-xref: delta_mono_mass "100.016044"
-xref: delta_avge_mass "100.0728"
-xref: delta_composition "H(4) C(4) O(3)"
-xref: username_of_poster "xwei"
-xref: group_of_poster ""
-xref: date_time_posted "2009-07-15 23:43:13"
-xref: date_time_modified "2010-11-24 17:59:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:923
-name: Label:13C(4)15N(2)+GG
-def: "13C(4) 15N(2) Lysine glygly." [PMID:12716131, URL:http\://www.pil.sdu.dk/silac_intro.htm, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=923]
-synonym: "heavy glygly lysine" RELATED []
-xref: record_id "923"
-xref: delta_mono_mass "120.050417"
-xref: delta_avge_mass "120.0601"
-xref: delta_composition "H(6) 13C(4) 15N(2) O(2)"
-xref: username_of_poster "mpcusack"
-xref: group_of_poster ""
-xref: date_time_posted "2009-09-16 21:04:07"
-xref: date_time_modified "2014-07-09 16:53:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "Used in SILAC PTM (glygly) experiment"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:926
-name: ethylamino
-def: "Ethyl amino." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=926]
-comment: Product of beta elimination of phospho- or glycosylated-Ser with addition of ethylamine.
-xref: record_id "926"
-xref: delta_mono_mass "27.047285"
-xref: delta_avge_mass "27.0684"
-xref: delta_composition "H(5) C(2) N O(-1)"
-xref: username_of_poster "cbatthya"
-xref: group_of_poster ""
-xref: date_time_posted "2009-09-17 20:37:18"
-xref: date_time_modified "2009-10-02 18:21:10"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:928
-name: MercaptoEthanol
-def: "2-OH-ethyl thio-Ser." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=928]
-comment: Product of beta elimination of phospho- or glycosylated-Ser with addition of beta Mercapto Ethanol.
-xref: record_id "928"
-xref: delta_mono_mass "60.003371"
-xref: delta_avge_mass "60.1182"
-xref: delta_composition "H(4) C(2) S"
-xref: username_of_poster "cbatthya"
-xref: group_of_poster ""
-xref: date_time_posted "2009-09-17 20:43:13"
-xref: date_time_modified "2009-10-02 18:23:38"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:931
-name: Ethyl+Deamidated
-def: "Deamidation followed by esterification with ethanol." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=931]
-xref: record_id "931"
-xref: delta_mono_mass "29.015316"
-xref: delta_avge_mass "29.0379"
-xref: delta_composition "H(3) C(2) N(-1) O"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2009-09-22 11:05:21"
-xref: date_time_modified "2012-08-06 14:58:24"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "Q"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:932
-name: VFQQQTGG
-def: "SUMOylation by SUMO-2/3 (formic acid cleavage)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=932]
-synonym: "ValPheGlnGlnGlnThrGlyGly" RELATED []
-xref: record_id "932"
-xref: delta_mono_mass "845.403166"
-xref: delta_avge_mass "845.8991"
-xref: delta_composition "H(55) C(37) N(11) O(12)"
-xref: username_of_poster "oosula"
-xref: group_of_poster ""
-xref: date_time_posted "2009-09-24 16:11:11"
-xref: date_time_modified "2010-02-02 18:25:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_1_misc_notes "This peptide is generated from a formic acid digest"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:933
-name: VIEVYQEQTGG
-def: "SUMOylation by SUMO-1 (formic acid cleavage)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=933]
-synonym: "ValIleGluValTyrGlnGluGlnThrGlyGly" RELATED []
-xref: record_id "933"
-xref: delta_mono_mass "1203.577168"
-xref: delta_avge_mass "1204.2859"
-xref: delta_composition "H(81) C(53) N(13) O(19)"
-xref: username_of_poster "oosula"
-xref: group_of_poster ""
-xref: date_time_posted "2009-09-24 16:15:34"
-xref: date_time_modified "2009-10-02 18:31:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:934
-name: AMTzHexNAc2
-def: "Photocleavable Biotin + GalNAz on O-GlcNAc." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=934]
-xref: record_id "934"
-xref: delta_mono_mass "502.202341"
-xref: delta_avge_mass "502.4757"
-xref: delta_composition "H(30) C(19) N(6) O(10)"
-xref: username_of_poster "mskim"
-xref: group_of_poster ""
-xref: date_time_posted "2009-10-08 18:05:00"
-xref: date_time_modified "2010-10-03 13:45:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:935
-name: Atto495Maleimide
-def: "High molecular absorption maleimide label for proteins." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=935]
-xref: record_id "935"
-xref: delta_mono_mass "474.250515"
-xref: delta_avge_mass "474.5747"
-xref: delta_composition "H(32) C(27) N(5) O(3)"
-xref: username_of_poster "anikolakakis"
-xref: group_of_poster ""
-xref: date_time_posted "2009-10-14 18:48:56"
-xref: date_time_modified "2009-10-16 14:34:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:936
-name: Chlorination
-def: "Chlorination of tyrosine residues." [PMID:14660678, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=936]
-xref: record_id "936"
-xref: delta_mono_mass "33.961028"
-xref: delta_avge_mass "34.4451"
-xref: delta_composition "H(-1) Cl"
-xref: username_of_poster "Bryan"
-xref: group_of_poster ""
-xref: date_time_posted "2009-10-15 17:07:41"
-xref: date_time_modified "2017-11-08 16:03:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "W"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:937
-name: dichlorination
-def: "Dichlorination." [PMID:11733505, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=937]
-xref: record_id "937"
-xref: delta_mono_mass "67.922055"
-xref: delta_avge_mass "68.8901"
-xref: delta_composition "H(-2) Cl(2)"
-xref: username_of_poster "Bryan"
-xref: group_of_poster ""
-xref: date_time_posted "2009-10-15 17:12:42"
-xref: date_time_modified "2014-05-19 10:13:24"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:938
-name: AROD
-def: "Cysteine modifier." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=938]
-comment: The electrophilic moiety of the chemical forms a direct bond with the thiol bond of the cysteine. As a result, there are no losses of elements and the final adduct has the monoisotopic mass of the chemical at 820.3360 added to a cysteine at SH side chain.
-xref: record_id "938"
-xref: delta_mono_mass "820.336015"
-xref: delta_avge_mass "820.979"
-xref: delta_composition "H(52) C(35) N(10) O(9) S(2)"
-xref: username_of_poster "hbromage"
-xref: group_of_poster ""
-xref: date_time_posted "2009-10-15 19:27:20"
-xref: date_time_modified "2009-10-16 14:41:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:939
-name: Cys->methylaminoAla
-def: "Carbamidomethylated Cys that undergoes beta-elimination and Michael addition of methylamine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=939]
-xref: record_id "939"
-xref: delta_mono_mass "-2.945522"
-xref: delta_avge_mass "-3.0238"
-xref: delta_composition "H(3) C N S(-1)"
-xref: username_of_poster "cbatthya"
-xref: group_of_poster ""
-xref: date_time_posted "2009-10-16 13:50:33"
-xref: date_time_modified "2009-10-16 14:44:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:940
-name: Cys->ethylaminoAla
-def: "Carbamidomethylated Cys that undergoes beta-elimination and Michael addition of ethylamine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=940]
-xref: record_id "940"
-xref: delta_mono_mass "11.070128"
-xref: delta_avge_mass "11.0028"
-xref: delta_composition "H(5) C(2) N S(-1)"
-xref: username_of_poster "cbatthya"
-xref: group_of_poster ""
-xref: date_time_posted "2009-10-16 13:53:46"
-xref: date_time_modified "2009-10-16 14:44:21"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:941
-name: DNPS
-def: "2,4-Dinitrobenzenesulfenyl." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=941]
-synonym: "Trp modification with 2,4-Dinitrobenzenesulfenyl" RELATED []
-xref: record_id "941"
-xref: delta_mono_mass "198.981352"
-xref: delta_avge_mass "199.164"
-xref: delta_composition "H(3) C(6) N(2) O(4) S"
-xref: username_of_poster "odra.pinato"
-xref: group_of_poster ""
-xref: date_time_posted "2009-10-19 13:08:56"
-xref: date_time_modified "2009-10-30 18:23:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "Fontana A. Biochemistry. vol 7. 980-986 (1968)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "W"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_2_misc_notes "derivatization of Trp residues using the 2,4-dinitrophenyl-sulfenyl chloride (DNPS-Cl) reagent, that leads to a Trp derivative with the DNPS label attached at 2-position of the indole nucleus."
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:942
-name: SulfoGMBS
-def: "High molecular absorption label for proteins." [URL:http\://www.piercenet.com/files/1763dh4.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=942]
-xref: record_id "942"
-xref: delta_mono_mass "458.162391"
-xref: delta_avge_mass "458.5306"
-xref: delta_composition "H(26) C(22) N(4) O(5) S"
-xref: username_of_poster "anikolakakis"
-xref: group_of_poster ""
-xref: date_time_posted "2009-10-26 19:28:04"
-xref: date_time_modified "2009-11-13 17:02:06"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:943
-name: DimethylamineGMBS
-def: "Modified GMBS X linker." [URL:http\://tools.thermofisher.com/content/sfs/manuals/MAN0011551_GMBS_SulfoGMBS_UG.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=943]
-xref: record_id "943"
-xref: delta_mono_mass "267.158292"
-xref: delta_avge_mass "267.3241"
-xref: delta_composition "H(21) C(13) N(3) O(3)"
-xref: username_of_poster "anikolakakis"
-xref: group_of_poster ""
-xref: date_time_posted "2009-11-04 20:26:57"
-xref: date_time_modified "2017-01-18 11:52:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:944
-name: Label:15N(2)2H(9)
-def: "SILAC label." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=944]
-synonym: "Label:15N(2)2H(9)" RELATED []
-xref: record_id "944"
-xref: delta_mono_mass "11.050561"
-xref: delta_avge_mass "11.0423"
-xref: delta_composition "H(-9) 2H(9) N(-2) 15N(2)"
-xref: username_of_poster "mskim"
-xref: group_of_poster ""
-xref: date_time_posted "2009-11-25 22:32:49"
-xref: date_time_modified "2009-12-07 20:03:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:946
-name: LG-anhydrolactam
-def: "Levuglandinyl-lysine anhydrolactam adduct." [PMID:10413514, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=946]
-xref: record_id "946"
-xref: delta_mono_mass "314.188195"
-xref: delta_avge_mass "314.4186"
-xref: delta_composition "H(26) C(20) O(3)"
-xref: username_of_poster "wridenour"
-xref: group_of_poster ""
-xref: date_time_posted "2010-01-12 01:08:28"
-xref: date_time_modified "2011-06-08 18:01:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:947
-name: LG-pyrrole
-def: "Levuglandinyl-lysine pyrrole adduct." [PMID:10413514, URL:http\://www.hmdb.ca/metabolites/HMDB0005079, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=947]
-xref: record_id "947"
-xref: delta_mono_mass "316.203845"
-xref: delta_avge_mass "316.4345"
-xref: delta_composition "H(28) C(20) O(3)"
-xref: username_of_poster "wridenour"
-xref: group_of_poster ""
-xref: date_time_posted "2010-01-12 01:12:38"
-xref: date_time_modified "2020-01-21 14:42:42"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "C"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-xref: spec_3_misc_notes "15-deoxy-PGJ2 (15d-PGJ2) influences multiple signaling pathways by covalently binding with key signaling molecules"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:948
-name: LG-anhyropyrrole
-def: "Levuglandinyl-lysine anhyropyrrole adduct." [PMID:10413514, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=948]
-xref: record_id "948"
-xref: delta_mono_mass "298.19328"
-xref: delta_avge_mass "298.4192"
-xref: delta_composition "H(26) C(20) O(2)"
-xref: username_of_poster "wridenour"
-xref: group_of_poster ""
-xref: date_time_posted "2010-01-12 01:14:46"
-xref: date_time_modified "2011-06-08 17:59:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:949
-name: 3-deoxyglucosone
-def: "Condensation product of 3-deoxyglucosone." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=949]
-xref: record_id "949"
-xref: delta_mono_mass "144.042259"
-xref: delta_avge_mass "144.1253"
-xref: delta_composition "H(8) C(6) O(4)"
-xref: username_of_poster "kimzey"
-xref: group_of_poster ""
-xref: date_time_posted "2010-01-15 18:19:17"
-xref: date_time_modified "2024-08-12 10:04:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Multiple"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:950
-name: Cation:Li
-def: "Replacement of proton by lithium." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=950]
-xref: record_id "950"
-xref: delta_mono_mass "6.008178"
-xref: delta_avge_mass "5.9331"
-xref: delta_composition "H(-1) Li"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2010-01-20 12:17:12"
-xref: date_time_modified "2010-01-20 12:17:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:951
-name: Cation:Ca[II]
-def: "Replacement of 2 protons by calcium." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=951]
-xref: record_id "951"
-xref: delta_mono_mass "37.946941"
-xref: delta_avge_mass "38.0621"
-xref: delta_composition "H(-2) Ca"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2010-01-20 12:20:03"
-xref: date_time_modified "2010-01-20 12:36:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:952
-name: Cation:Fe[II]
-def: "Replacement of 2 protons by iron." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=952]
-xref: record_id "952"
-xref: delta_mono_mass "53.919289"
-xref: delta_avge_mass "53.8291"
-xref: delta_composition "H(-2) Fe"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2010-01-20 12:21:03"
-xref: date_time_modified "2010-01-20 12:21:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:953
-name: Cation:Ni[II]
-def: "Replacement of 2 protons by nickel." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=953]
-xref: record_id "953"
-xref: delta_mono_mass "55.919696"
-xref: delta_avge_mass "56.6775"
-xref: delta_composition "H(-2) Ni"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2010-01-20 12:22:52"
-xref: date_time_modified "2010-01-20 12:22:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:954
-name: Cation:Zn[II]
-def: "Replacement of 2 protons by zinc." [URL:http\://www.uniprot.org/uniprot/P07509, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=954]
-xref: record_id "954"
-xref: delta_mono_mass "61.913495"
-xref: delta_avge_mass "63.3931"
-xref: delta_composition "H(-2) Zn"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2010-01-20 12:23:59"
-xref: date_time_modified "2015-03-19 09:31:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "H"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:955
-name: Cation:Ag
-def: "Replacement of proton by silver." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=955]
-xref: record_id "955"
-xref: delta_mono_mass "105.897267"
-xref: delta_avge_mass "106.8603"
-xref: delta_composition "H(-1) Ag"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2010-01-20 12:30:59"
-xref: date_time_modified "2010-01-20 12:30:59"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:956
-name: Cation:Mg[II]
-def: "Replacement of 2 protons by magnesium." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=956]
-xref: record_id "956"
-xref: delta_mono_mass "21.969392"
-xref: delta_avge_mass "22.2891"
-xref: delta_composition "H(-2) Mg"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2010-01-20 12:36:18"
-xref: date_time_modified "2010-01-20 12:36:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:957
-name: 2-succinyl
-def: "S-(2-succinyl) cysteine." [PMID:18448829, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=957]
-xref: record_id "957"
-xref: delta_mono_mass "116.010959"
-xref: delta_avge_mass "116.0722"
-xref: delta_composition "H(4) C(4) O(4)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2010-01-26 09:57:53"
-xref: date_time_modified "2010-10-15 15:51:20"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:958
-name: Propargylamine
-def: "Propargylamine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=958]
-xref: record_id "958"
-xref: delta_mono_mass "37.031634"
-xref: delta_avge_mass "37.0632"
-xref: delta_composition "H(3) C(3) N O(-1)"
-xref: username_of_poster "ywswansea"
-xref: group_of_poster ""
-xref: date_time_posted "2010-01-26 14:37:33"
-xref: date_time_modified "2010-02-01 09:26:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Any C-term"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "D"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "E"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:959
-name: Phosphopropargyl
-def: "Phospho-propargylamine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=959]
-xref: record_id "959"
-xref: delta_mono_mass "116.997965"
-xref: delta_avge_mass "117.0431"
-xref: delta_composition "H(4) C(3) N O(2) P"
-xref: username_of_poster "ywswansea"
-xref: group_of_poster ""
-xref: date_time_posted "2010-01-26 14:42:08"
-xref: date_time_modified "2010-02-01 09:25:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Multiple"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Multiple"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Multiple"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:960
-name: SUMO2135
-def: "SUMOylation by SUMO-1 after tryptic cleavage." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=960]
-synonym: "ELGMEEEDVIEVYQEQTGG" RELATED []
-xref: record_id "960"
-xref: delta_mono_mass "2135.920496"
-xref: delta_avge_mass "2137.2343"
-xref: delta_composition "H(137) C(90) N(21) O(37) S"
-xref: username_of_poster "oosula"
-xref: group_of_poster ""
-xref: date_time_posted "2010-02-02 18:17:15"
-xref: date_time_modified "2010-02-14 11:28:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:961
-name: SUMO3549
-def: "SUMOylation by SUMO-2/3 after tryptic cleavage." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=961]
-synonym: "FDGQPINETDTPAQLEMEDEDTIDVFQQQTGG" RELATED []
-xref: record_id "961"
-xref: delta_mono_mass "3549.536568"
-xref: delta_avge_mass "3551.6672"
-xref: delta_composition "H(224) C(150) N(38) O(60) S"
-xref: username_of_poster "oosula"
-xref: group_of_poster ""
-xref: date_time_posted "2010-02-02 18:21:23"
-xref: date_time_modified "2010-02-14 11:27:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:967
-name: thioacylPA
-def: "Membrane protein extraction." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=967]
-xref: record_id "967"
-xref: delta_mono_mass "159.035399"
-xref: delta_avge_mass "159.2062"
-xref: delta_composition "H(9) C(6) N O(2) S"
-xref: username_of_poster "tmiwamoto"
-xref: group_of_poster ""
-xref: date_time_posted "2010-02-05 06:00:39"
-xref: date_time_modified "2010-04-05 21:31:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:971
-name: maleimide3
-def: "Maleimide-3-saccharide." [PMID:18925771, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=971]
-comment: Created for Bindu Abraham 12/22/09.
-xref: record_id "971"
-xref: delta_mono_mass "969.366232"
-xref: delta_avge_mass "969.8975"
-xref: delta_composition "H(59) C(37) N(7) O(23)"
-xref: username_of_poster "hooverdm"
-xref: group_of_poster ""
-xref: date_time_posted "2010-02-12 17:23:33"
-xref: date_time_modified "2010-04-05 21:30:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:972
-name: maleimide5
-def: "Maleimide-5-saccharide." [PMID:18925771, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=972]
-comment: Created for Bindu Abraham 12/22/09.
-xref: record_id "972"
-xref: delta_mono_mass "1293.471879"
-xref: delta_avge_mass "1294.1787"
-xref: delta_composition "H(79) C(49) N(7) O(33)"
-xref: username_of_poster "hooverdm"
-xref: group_of_poster ""
-xref: date_time_posted "2010-02-12 17:25:52"
-xref: date_time_modified "2010-04-05 21:29:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:973
-name: Puromycin
-def: "Puromycin." [PMID:10666460, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=973]
-comment: Created for Michael (Brad) Strader 2/12/10.
-xref: record_id "973"
-xref: delta_mono_mass "453.212452"
-xref: delta_avge_mass "453.4943"
-xref: delta_composition "H(27) C(22) N(7) O(4)"
-xref: username_of_poster "hooverdm"
-xref: group_of_poster ""
-xref: date_time_posted "2010-02-12 20:50:31"
-xref: date_time_modified "2010-04-12 15:38:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Any C-term"
-xref: spec_1_classification "Co-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:977
-name: Carbofuran
-def: "2,3-dihydro-2,2-dimethyl-7-benzofuranol N-methyl carbamate." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=977]
-xref: record_id "977"
-xref: delta_mono_mass "57.021464"
-xref: delta_avge_mass "57.0513"
-xref: delta_composition "H(3) C(2) N O"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2010-02-24 21:10:32"
-xref: date_time_modified "2021-06-30 18:27:33"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:978
-name: BITC
-def: "Benzyl isothiocyanate." [PMID:22835833, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=978]
-xref: record_id "978"
-xref: delta_mono_mass "149.02992"
-xref: delta_avge_mass "149.2129"
-xref: delta_composition "H(7) C(8) N S"
-xref: username_of_poster "miyoshin"
-xref: group_of_poster ""
-xref: date_time_posted "2010-03-09 09:42:12"
-xref: date_time_modified "2013-04-26 06:26:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:979
-name: PEITC
-def: "Phenethyl isothiocyanate." [PMID:22835833, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=979]
-xref: record_id "979"
-xref: delta_mono_mass "163.04557"
-xref: delta_avge_mass "163.2395"
-xref: delta_composition "H(9) C(9) N S"
-xref: username_of_poster "miyoshin"
-xref: group_of_poster ""
-xref: date_time_posted "2010-03-09 10:06:18"
-xref: date_time_modified "2013-04-26 06:27:10"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:981
-name: glucosone
-def: "Condensation product of glucosone." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=981]
-xref: record_id "981"
-xref: delta_mono_mass "160.037173"
-xref: delta_avge_mass "160.1247"
-xref: delta_composition "H(8) C(6) O(5)"
-xref: username_of_poster "kimzey"
-xref: group_of_poster ""
-xref: date_time_posted "2010-03-31 00:28:53"
-xref: date_time_modified "2010-04-05 21:25:21"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:984
-name: cysTMT
-def: "Native cysteine-reactive Tandem Mass Tag®." [URL:http\://bit.ly/1GBnaC8, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=984]
-comment: This modification describes the native cysteine-reactive cysTMT Reagent without isotopic label. Upon CID, this reagent releases a reporter ion of 126.127725 (monoisotopic mass).
-synonym: "Tandem Mass Tag® and TMT® are registered Trademarks of Proteome Sciences plc." RELATED []
-xref: record_id "984"
-xref: delta_mono_mass "299.166748"
-xref: delta_avge_mass "299.4322"
-xref: delta_composition "H(25) C(14) N(3) O(2) S"
-xref: username_of_poster "jorogers6"
-xref: group_of_poster ""
-xref: date_time_posted "2010-04-22 21:57:44"
-xref: date_time_modified "2024-08-12 10:07:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:985
-name: cysTMT6plex
-def: "Cysteine-reactive Sixplex Tandem Mass Tag®." [URL:http\://bit.ly/1GBnaC8, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=985]
-comment: This modification describes the isobaric sixplex cysteine-reactive cysTMT6 Reagents with isotopic labels. Upon CID, these reagents release reporter ions of 126.127725, 127.131079, 128.134433, 129.137787, 130.141141, and 131.138176 (monoisotopic mass).
-synonym: "Tandem Mass Tag® and TMT® are registered Trademarks of Proteome Sciences plc." RELATED []
-xref: record_id "985"
-xref: delta_mono_mass "304.177202"
-xref: delta_avge_mass "304.3962"
-xref: delta_composition "H(25) C(10) 13C(4) N(2) 15N O(2) S"
-xref: username_of_poster "jorogers6"
-xref: group_of_poster ""
-xref: date_time_posted "2010-04-22 22:05:46"
-xref: date_time_modified "2024-08-12 10:07:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:986
-name: Label:13C(6)+Dimethyl
-def: "Dimethyl 13C(6) Silac label." [FindMod:DIMETH, URL:http\://www.pil.sdu.dk/silac_intro.htm, PMID:http://www.ncbi.nlm.nih.gov/pubmed/14670044?dopt=AbstractPlus, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=986]
-xref: record_id "986"
-xref: delta_mono_mass "34.051429"
-xref: delta_avge_mass "34.0091"
-xref: delta_composition "H(4) C(-4) 13C(6)"
-xref: username_of_poster "glick2"
-xref: group_of_poster ""
-xref: date_time_posted "2010-05-09 10:48:19"
-xref: date_time_modified "2010-05-14 16:19:43"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "SILAC+PTM"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:987
-name: Label:13C(6)15N(2)+Dimethyl
-def: "Dimethyl 13C(6)15N(2) Silac label." [URL:http\://www.pil.sdu.dk/silac_intro.htm, FindMod:DIMETH, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=987]
-xref: record_id "987"
-xref: delta_mono_mass "36.045499"
-xref: delta_avge_mass "35.9959"
-xref: delta_composition "H(4) C(-4) 13C(6) N(-2) 15N(2)"
-xref: username_of_poster "glick2"
-xref: group_of_poster ""
-xref: date_time_posted "2010-05-09 10:57:55"
-xref: date_time_modified "2010-05-14 16:20:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "SILAC+PTM"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:989
-name: Ammonium
-def: "Replacement of proton with ammonium ion." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=989]
-comment: Sometimes observed after elution of phosphopeptides from TiO2 with ammonium hydroxide.
-xref: record_id "989"
-xref: delta_mono_mass "17.026549"
-xref: delta_avge_mass "17.0305"
-xref: delta_composition "H(3) N"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2010-05-18 10:32:03"
-xref: date_time_modified "2010-06-04 15:08:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Any C-term"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "E"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "D"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:991
-name: ISD_z+2_ion
-def: "ISD (z+2)-series." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=991]
-xref: record_id "991"
-xref: delta_mono_mass "-15.010899"
-xref: delta_avge_mass "-15.0146"
-xref: delta_composition "H(-1) N(-1)"
-xref: username_of_poster "suckau"
-xref: group_of_poster ""
-xref: date_time_posted "2010-06-08 09:42:52"
-xref: date_time_modified "2024-08-12 11:27:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Artefact"
-xref: spec_1_misc_notes "this is a virtual modification, as it only accounts for the structure of the MS/MS fragment as it occurs in Top-Down MS/MS analyses. This must be accounted for in MS³-analysis of z+2 ions"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:993
-name: Biotin:Sigma-B1267
-def: "Was Biotin-maleimide." [PMID:15449375, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=993]
-synonym: "maleimide biotinylated" RELATED []
-xref: record_id "993"
-xref: delta_mono_mass "449.17329"
-xref: delta_avge_mass "449.5239"
-xref: delta_composition "H(27) C(20) N(5) O(5) S"
-xref: username_of_poster "mpcusack"
-xref: group_of_poster ""
-xref: date_time_posted "2010-06-10 07:50:00"
-xref: date_time_modified "2010-12-03 16:02:22"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:994
-name: Label:15N(1)
-def: "15N(1)." [PMID:19664813, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=994]
-synonym: "Metabolic labeling with ammonium sulfate (15N)" RELATED []
-xref: record_id "994"
-xref: delta_mono_mass "0.997035"
-xref: delta_avge_mass "0.9934"
-xref: delta_composition "N(-1) 15N"
-xref: username_of_poster "ppicotti"
-xref: group_of_poster ""
-xref: date_time_posted "2010-06-22 14:52:08"
-xref: date_time_modified "2011-11-21 14:26:07"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "Y"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "G"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "A"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "S"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Isotopic label"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "P"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Isotopic label"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "V"
-xref: spec_7_position "Anywhere"
-xref: spec_7_classification "Isotopic label"
-xref: spec_8_group "8"
-xref: spec_8_hidden "1"
-xref: spec_8_site "T"
-xref: spec_8_position "Anywhere"
-xref: spec_8_classification "Isotopic label"
-xref: spec_9_group "9"
-xref: spec_9_hidden "1"
-xref: spec_9_site "C"
-xref: spec_9_position "Anywhere"
-xref: spec_9_classification "Isotopic label"
-xref: spec_10_group "10"
-xref: spec_10_hidden "1"
-xref: spec_10_site "I"
-xref: spec_10_position "Anywhere"
-xref: spec_10_classification "Isotopic label"
-xref: spec_11_group "11"
-xref: spec_11_hidden "1"
-xref: spec_11_site "L"
-xref: spec_11_position "Anywhere"
-xref: spec_11_classification "Isotopic label"
-xref: spec_12_group "12"
-xref: spec_12_hidden "1"
-xref: spec_12_site "D"
-xref: spec_12_position "Anywhere"
-xref: spec_12_classification "Isotopic label"
-xref: spec_13_group "13"
-xref: spec_13_hidden "1"
-xref: spec_13_site "E"
-xref: spec_13_position "Anywhere"
-xref: spec_13_classification "Isotopic label"
-xref: spec_14_group "14"
-xref: spec_14_hidden "1"
-xref: spec_14_site "M"
-xref: spec_14_position "Anywhere"
-xref: spec_14_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:995
-name: Label:15N(2)
-def: "15N(2)." [PMID:19664813, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=995]
-synonym: "Metabolic labeling with ammonium sulfate (15N)" RELATED []
-xref: record_id "995"
-xref: delta_mono_mass "1.99407"
-xref: delta_avge_mass "1.9868"
-xref: delta_composition "N(-2) 15N(2)"
-xref: username_of_poster "ppicotti"
-xref: group_of_poster ""
-xref: date_time_posted "2010-06-22 15:29:02"
-xref: date_time_modified "2011-11-21 14:26:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "Q"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "W"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:996
-name: Label:15N(3)
-def: "15N(3)." [PMID:19664813, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=996]
-synonym: "Metabolic labeling with ammonium sulfate (15N)" RELATED []
-xref: record_id "996"
-xref: delta_mono_mass "2.991105"
-xref: delta_avge_mass "2.9802"
-xref: delta_composition "N(-3) 15N(3)"
-xref: username_of_poster "ppicotti"
-xref: group_of_poster ""
-xref: date_time_posted "2010-06-22 15:30:28"
-xref: date_time_modified "2011-11-21 14:26:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:997
-name: sulfo+amino
-def: "Aminotyrosine with sulfation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=997]
-synonym: "amino_sulfate" RELATED []
-xref: record_id "997"
-xref: delta_mono_mass "94.967714"
-xref: delta_avge_mass "95.0778"
-xref: delta_composition "H N O(3) S"
-xref: username_of_poster "huidouzi"
-xref: group_of_poster ""
-xref: date_time_posted "2010-06-23 18:50:14"
-xref: date_time_modified "2010-06-28 10:29:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1000
-name: AHA-Alkyne
-def: "Azidohomoalanine (AHA) bound to propargylglycine-NH2 (alkyne)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1000]
-comment: Methionine (C5H11NO2S) is substituted in culture with azidohomoalanine (AHA - C4H8N4O2). The azide group reacts with the alkyne group propargylglycine-NH2. As a result the side chain of methionine (C3H7S) is substituted by C7H12N5O.
-xref: record_id "1000"
-xref: delta_mono_mass "107.077339"
-xref: delta_avge_mass "107.0504"
-xref: delta_composition "H(5) C(4) N(5) O S(-1)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2010-09-28 09:28:15"
-xref: date_time_modified "2010-10-03 13:44:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1001
-name: AHA-Alkyne-KDDDD
-def: "Azidohomoalanine (AHA) bound to DDDDK-propargylglycine-NH2 (alkyne)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1001]
-comment: Methionine (C5H11NO2S) is substituted in culture with azidohomoalanine (AHA - C4H8N4O2). The azide group reacts with the alkyne group DDDDK-propargylglycine-NH2. As a result the side chain of methionine (C3H7S) is substituted by C29H44N11O14.
-xref: record_id "1001"
-xref: delta_mono_mass "695.280074"
-xref: delta_avge_mass "695.5723"
-xref: delta_composition "H(37) C(26) N(11) O(14) S(-1)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2010-09-28 09:35:48"
-xref: date_time_modified "2010-10-03 13:44:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1002
-name: EGCG1
-def: "(-)-epigallocatechin-3-gallate." [PMID:18771724, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1002]
-comment: Created for Bindu Abraham 2010-10-05.
-xref: record_id "1002"
-xref: delta_mono_mass "456.069261"
-xref: delta_avge_mass "456.3558"
-xref: delta_composition "H(16) C(22) O(11)"
-xref: username_of_poster "hooverdm"
-xref: group_of_poster ""
-xref: date_time_posted "2010-10-05 20:46:40"
-xref: date_time_modified "2010-12-23 15:47:42"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1003
-name: EGCG2
-def: "(-)-dehydroepigallocatechin." [PMID:18771724, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1003]
-comment: Created for Bindu Abraham 2010-10-05.
-xref: record_id "1003"
-xref: delta_mono_mass "287.055563"
-xref: delta_avge_mass "287.2442"
-xref: delta_composition "H(11) C(15) O(6)"
-xref: username_of_poster "hooverdm"
-xref: group_of_poster ""
-xref: date_time_posted "2010-10-05 20:48:38"
-xref: date_time_modified "2010-12-23 15:47:33"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1004
-name: Label:13C(6)15N(4)+Methyl
-def: "Monomethylated Arg13C(6) 15N(4)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1004]
-xref: record_id "1004"
-xref: delta_mono_mass "24.023919"
-xref: delta_avge_mass "23.9561"
-xref: delta_composition "H(2) C(-5) 13C(6) N(-4) 15N(4)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2010-10-27 10:36:31"
-xref: date_time_modified "2010-11-05 16:47:36"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1005
-name: Label:13C(6)15N(4)+Dimethyl
-def: "Dimethylated Arg13C(6) 15N(4)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1005]
-xref: record_id "1005"
-xref: delta_mono_mass "38.039569"
-xref: delta_avge_mass "37.9827"
-xref: delta_composition "H(4) C(-4) 13C(6) N(-4) 15N(4)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2010-10-27 10:52:10"
-xref: date_time_modified "2010-11-05 16:49:29"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1006
-name: Label:13C(6)15N(4)+Methyl:2H(3)13C(1)
-def: "2H(3) 13C(1) monomethylated Arg13C(6) 15N(4)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1006]
-xref: record_id "1006"
-xref: delta_mono_mass "28.046104"
-xref: delta_avge_mass "27.9673"
-xref: delta_composition "H(-1) 2H(3) C(-6) 13C(7) N(-4) 15N(4)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2010-10-27 10:59:21"
-xref: date_time_modified "2010-11-05 16:53:21"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1007
-name: Label:13C(6)15N(4)+Dimethyl:2H(6)13C(2)
-def: "2H(6) 13C(2) Dimethylated Arg13C(6) 15N(4)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1007]
-xref: record_id "1007"
-xref: delta_mono_mass "46.083939"
-xref: delta_avge_mass "46.005"
-xref: delta_composition "H(-2) 2H(6) C(-6) 13C(8) N(-4) 15N(4)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2010-10-27 11:07:29"
-xref: date_time_modified "2010-11-05 16:54:24"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1008
-name: Cys->CamSec
-def: "Sec Iodoacetamide derivative." [PMID:18283440, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1008]
-synonym: "Carboxyamidomethylation of selenocysteine" RELATED []
-xref: record_id "1008"
-xref: delta_mono_mass "104.965913"
-xref: delta_avge_mass "103.9463"
-xref: delta_composition "H(3) C(2) N O S(-1) Se"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2010-11-04 12:00:12"
-xref: date_time_modified "2016-02-01 14:19:53"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Non-standard residue"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1009
-name: Thiazolidine
-def: "Formaldehyde adduct." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1009]
-synonym: "thiazolidine-2-carboxylic acid" RELATED []
-xref: record_id "1009"
-xref: delta_mono_mass "12"
-xref: delta_avge_mass "12.0107"
-xref: delta_composition "C"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2010-11-04 12:29:10"
-xref: date_time_modified "2017-03-30 16:37:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "R"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "H"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "Y"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "W"
-xref: spec_7_position "Anywhere"
-xref: spec_7_classification "Chemical derivative"
-xref: spec_8_group "8"
-xref: spec_8_hidden "1"
-xref: spec_8_site "F"
-xref: spec_8_position "Anywhere"
-xref: spec_8_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1010
-name: DEDGFLYMVYASQETFG
-def: "Addition of DEDGFLYMVYASQETFG." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1010]
-xref: record_id "1010"
-xref: delta_mono_mass "1970.824411"
-xref: delta_avge_mass "1972.088"
-xref: delta_composition "H(122) C(89) N(18) O(31) S"
-xref: username_of_poster "hbromage"
-xref: group_of_poster ""
-xref: date_time_posted "2010-11-04 17:27:46"
-xref: date_time_modified "2010-11-24 18:00:09"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_1_neutral_loss_19_mono_mass "18.010565"
-xref: spec_1_neutral_loss_19_avge_mass "18.0153"
-xref: spec_1_neutral_loss_19_flag "false"
-xref: spec_1_neutral_loss_19_composition "Water"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1012
-name: Biotin:Invitrogen-M1602
-def: "Nalpha-(3-maleimidylpropionyl)biocytin." [URL:http\://products.invitrogen.com/ivgn/product/M1602?ICID=search-m1602, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1012]
-synonym: "Reference M1602 Invitrogen" RELATED []
-xref: record_id "1012"
-xref: delta_mono_mass "523.210069"
-xref: delta_avge_mass "523.6024"
-xref: delta_composition "H(33) C(23) N(5) O(7) S"
-xref: username_of_poster "camoin"
-xref: group_of_poster ""
-xref: date_time_posted "2010-11-16 10:11:53"
-xref: date_time_modified "2010-12-03 15:58:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1014
-name: glycidamide
-def: "Glycidamide adduct." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1014]
-xref: record_id "1014"
-xref: delta_mono_mass "87.032028"
-xref: delta_avge_mass "87.0773"
-xref: delta_composition "H(5) C(3) N O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2010-12-21 17:00:41"
-xref: date_time_modified "2024-08-12 09:49:53"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1015
-name: Ahx2+Hsl
-def: "C-terminal homoserine lactone and two aminohexanoic acids." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1015]
-xref: record_id "1015"
-xref: delta_mono_mass "309.205242"
-xref: delta_avge_mass "309.4039"
-xref: delta_composition "H(27) C(16) N(3) O(3)"
-xref: username_of_poster "kpkent"
-xref: group_of_poster ""
-xref: date_time_posted "2010-12-22 10:13:01"
-xref: date_time_modified "2011-01-07 17:06:08"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Any C-term"
-xref: spec_1_classification "Non-standard residue"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1017
-name: DMPO
-def: "DMPO spin-trap nitrone adduct." [PMID:18160050, PMID:17637042, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1017]
-comment: Created for Bindu Abraham 2011-01-25.
-xref: record_id "1017"
-xref: delta_mono_mass "111.068414"
-xref: delta_avge_mass "111.1418"
-xref: delta_composition "H(9) C(6) N O"
-xref: username_of_poster "hooverdm"
-xref: group_of_poster ""
-xref: date_time_posted "2011-01-25 18:30:32"
-xref: date_time_modified "2011-02-28 17:17:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1018
-name: ICDID
-def: "Isotope-Coded Dimedone light form." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1018]
-xref: record_id "1018"
-xref: delta_mono_mass "138.06808"
-xref: delta_avge_mass "138.1638"
-xref: delta_composition "H(10) C(8) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-02-02 17:23:34"
-xref: date_time_modified "2011-02-02 17:23:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1019
-name: ICDID:2H(6)
-def: "Isotope-Coded Dimedone heavy form." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1019]
-xref: record_id "1019"
-xref: delta_mono_mass "144.10574"
-xref: delta_avge_mass "144.2008"
-xref: delta_composition "H(4) 2H(6) C(8) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-02-02 17:24:45"
-xref: date_time_modified "2011-02-02 17:24:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1020
-name: Xlink:DSS[156]
-def: "Water-quenched monolink of DSS/BS3 crosslinker." [PMID:8326953, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1020]
-xref: record_id "1020"
-xref: delta_mono_mass "156.078644"
-xref: delta_avge_mass "156.1791"
-xref: delta_composition "H(12) C(8) O(3)"
-xref: username_of_poster "Kramerh"
-xref: group_of_poster ""
-xref: date_time_posted "2011-02-07 14:20:22"
-xref: date_time_modified "2017-08-17 15:09:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1021
-name: Xlink:EGS[244]
-def: "Water quenched monolink of EGS cross-linker." [PMID:36892, URL:https\://tools.thermofisher.com/content/sfs/manuals/MAN0011281_EGS_SulfoEGS_UG.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1021]
-synonym: "Ethylene glycolbis(succinimidylsuccinate)" RELATED []
-xref: record_id "1021"
-xref: delta_mono_mass "244.058303"
-xref: delta_avge_mass "244.1981"
-xref: delta_composition "H(12) C(10) O(7)"
-xref: username_of_poster "Kramerh"
-xref: group_of_poster ""
-xref: date_time_posted "2011-02-07 17:40:36"
-xref: date_time_modified "2017-08-17 15:10:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1022
-name: Xlink:DST[132]
-def: "Water quenched monolink of DST crosslinker." [PMID:212103, URL:https\://assets.thermofisher.com/TFS-Assets/LSG/manuals/MAN0011282_DST_UG.pdf, PMID:3001048, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1022]
-xref: record_id "1022"
-xref: delta_mono_mass "132.005873"
-xref: delta_avge_mass "132.0716"
-xref: delta_composition "H(4) C(4) O(5)"
-xref: username_of_poster "Kramerh"
-xref: group_of_poster ""
-xref: date_time_posted "2011-02-07 18:02:58"
-xref: date_time_modified "2017-08-18 14:26:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1023
-name: Xlink:DTSSP[192]
-def: "Water quenched monolink of DSP/DTSSP crosslinker." [URL:https\://tools.thermofisher.com/content/sfs/manuals/MAN0011280_DTSSP_DSP_UG.pdf, PMID:1262347, PMID:8457554, PMID:322714, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1023]
-synonym: "Also known as DSP" RELATED []
-xref: record_id "1023"
-xref: delta_mono_mass "191.991486"
-xref: delta_avge_mass "192.2559"
-xref: delta_composition "H(8) C(6) O(3) S(2)"
-xref: username_of_poster "Kramerh"
-xref: group_of_poster ""
-xref: date_time_posted "2011-02-07 18:22:31"
-xref: date_time_modified "2017-08-18 14:53:07"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1024
-name: Xlink:SMCC[237]
-def: "Water quenched monolink of SMCC." [PMID:6490581, PMID:1931231, URL:https\://assets.thermofisher.com/TFS-Assets/LSG/manuals/MAN0011295_SMCC_SulfoSMCC_UG.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1024]
-xref: record_id "1024"
-xref: delta_mono_mass "237.100108"
-xref: delta_avge_mass "237.2518"
-xref: delta_composition "H(15) C(12) N O(4)"
-xref: username_of_poster "Kramerh"
-xref: group_of_poster ""
-xref: date_time_posted "2011-02-07 19:33:39"
-xref: date_time_modified "2017-09-05 15:09:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1027
-name: Xlink:DMP[140]
-def: "Water quenched monolink of DMP crosslinker." [PMID:2144419, PMID:14696200, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1027]
-synonym: "Dimethyl pimelimidate dead-end crosslink" RELATED []
-xref: record_id "1027"
-xref: delta_mono_mass "140.094963"
-xref: delta_avge_mass "140.183"
-xref: delta_composition "H(12) C(7) N(2) O"
-xref: username_of_poster "Kramerh"
-xref: group_of_poster ""
-xref: date_time_posted "2011-02-25 16:18:13"
-xref: date_time_modified "2017-08-18 10:17:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1028
-name: Xlink:EGS[115]
-def: "Cleavage product of EGS protein crosslinks by hydroylamine treatment." [PMID:36892, URL:https\://tools.thermofisher.com/content/sfs/manuals/MAN0011281_EGS_SulfoEGS_UG.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1028]
-synonym: "Ethylene glycolbis(succinimidylsuccinate)" RELATED []
-xref: record_id "1028"
-xref: delta_mono_mass "115.026943"
-xref: delta_avge_mass "115.0874"
-xref: delta_composition "H(5) C(4) N O(3)"
-xref: username_of_poster "Kramerh"
-xref: group_of_poster ""
-xref: date_time_posted "2011-02-25 17:16:45"
-xref: date_time_modified "2017-08-17 15:10:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1031
-name: Biotin:Thermo-88310
-def: "Desthiobiotin modification of lysine." [URL:http\://www.lifetechnologies.com/order/catalog/product/88310, URL:http\://www.lifetechnologies.com/order/catalog/product/88314, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1031]
-synonym: "desthiobiotin-GTP desthiobiotin-ADP desthiobiotin-ATP" RELATED []
-xref: record_id "1031"
-xref: delta_mono_mass "196.121178"
-xref: delta_avge_mass "196.2462"
-xref: delta_composition "H(16) C(10) N(2) O(2)"
-xref: username_of_poster "rbomgard"
-xref: group_of_poster ""
-xref: date_time_posted "2011-03-02 20:33:20"
-xref: date_time_modified "2015-04-20 16:11:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1032
-name: 2-nitrobenzyl
-def: "Tyrosine caged with 2-nitrobenzyl (ONB)." [PMID:16548032, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1032]
-xref: record_id "1032"
-xref: delta_mono_mass "135.032028"
-xref: delta_avge_mass "135.1201"
-xref: delta_composition "H(5) C(7) N O(2)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2011-03-14 10:56:33"
-xref: date_time_modified "2011-03-18 13:39:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1033
-name: Cys->SecNEM
-def: "N-ethylmaleimide on selenocysteines." [URL:http\://www.chemistry.ucsc.edu/~fink/231/Image118.gif, PMID:18283440, PMID:12777388, PMID:11813307, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1033]
-synonym: "SecNEM" RELATED []
-xref: record_id "1033"
-xref: delta_mono_mass "172.992127"
-xref: delta_avge_mass "172.0203"
-xref: delta_composition "H(7) C(6) N O(2) S(-1) Se"
-xref: username_of_poster "mpcusack"
-xref: group_of_poster ""
-xref: date_time_posted "2011-03-31 18:29:45"
-xref: date_time_modified "2016-02-01 14:20:14"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Non-standard residue"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1034
-name: Cys->SecNEM:2H(5)
-def: "D5 N-ethylmaleimide on selenocysteines." [PMID:18283440, PMID:12777388, URL:http\://www.chemistry.ucsc.edu/~fink/231/Image118.gif, PMID:11813307, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1034]
-synonym: "SecNEM D5" RELATED []
-xref: record_id "1034"
-xref: delta_mono_mass "178.023511"
-xref: delta_avge_mass "177.0511"
-xref: delta_composition "H(2) 2H(5) C(6) N O(2) S(-1) Se"
-xref: username_of_poster "mpcusack"
-xref: group_of_poster ""
-xref: date_time_posted "2011-03-31 18:32:32"
-xref: date_time_modified "2016-02-01 14:20:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1035
-name: Thiadiazole
-def: "Thiadiazolydation of Cys." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1035]
-xref: record_id "1035"
-xref: delta_mono_mass "174.025169"
-xref: delta_avge_mass "174.2223"
-xref: delta_composition "H(6) C(9) N(2) S"
-xref: username_of_poster "cbatthya"
-xref: group_of_poster ""
-xref: date_time_posted "2011-04-01 16:26:52"
-xref: date_time_modified "2011-04-08 16:38:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1036
-name: Withaferin
-def: "Modification of cystein by withaferin." [PMID:http://www.ncbi.nlm.nih.gov/pubmed/21432907, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1036]
-xref: record_id "1036"
-xref: delta_mono_mass "470.266839"
-xref: delta_avge_mass "470.5977"
-xref: delta_composition "H(38) C(28) O(6)"
-xref: username_of_poster "ProtUA"
-xref: group_of_poster ""
-xref: date_time_posted "2011-04-06 12:31:40"
-xref: date_time_modified "2011-04-08 16:37:15"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1037
-name: Biotin:Thermo-88317
-def: "Desthiobiotin fluorophosphonate." [URL:http\://www.lifetechnologies.com/order/catalog/product/88317, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1037]
-comment: Dethiobiotin-FP was designed to label the active site serine of serine hydrolases (e.g. esterases, peptidases, lipases).
-synonym: "desthiobiotin-alkyl-FP desthiobiotin-FP" RELATED []
-xref: record_id "1037"
-xref: delta_mono_mass "443.291294"
-xref: delta_avge_mass "443.5603"
-xref: delta_composition "H(42) C(22) N(3) O(4) P"
-xref: username_of_poster "rbomgard"
-xref: group_of_poster ""
-xref: date_time_posted "2011-05-06 19:40:48"
-xref: date_time_modified "2015-04-20 16:24:29"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1038
-name: TAMRA-FP
-def: "TAMRA fluorophosphonate modification of serine." [URL:http\://www.piercenet.com/browse.cfm?fldID=0842EF3A-D867-AEA2-6E77-E84116CAA87C, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1038]
-comment: TAMRA-FP was designed to label the active site serine of serine hydrolases (e.g. esterases, peptidases, lipases).
-synonym: "ActivX TAMRA-FP Serine Hydrolase Probe TAMRA-alkyl-FP" RELATED []
-xref: record_id "1038"
-xref: delta_mono_mass "659.312423"
-xref: delta_avge_mass "659.7514"
-xref: delta_composition "H(46) C(37) N(3) O(6) P"
-xref: username_of_poster "rbomgard"
-xref: group_of_poster ""
-xref: date_time_posted "2011-05-06 20:03:27"
-xref: date_time_modified "2011-05-09 16:01:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "Y"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1039
-name: Biotin:Thermo-21901+H2O
-def: "Maleimide-Biotin + Water." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1039]
-synonym: "Maleimide-PEG2-Biotin + Water" RELATED []
-xref: record_id "1039"
-xref: delta_mono_mass "543.236284"
-xref: delta_avge_mass "543.6336"
-xref: delta_composition "H(37) C(23) N(5) O(8) S"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2011-05-18 16:28:42"
-xref: date_time_modified "2011-05-25 16:02:07"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1041
-name: Deoxyhypusine
-def: "Deoxyhypusine." [PMID:20942800, PMID:10542236, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1041]
-comment: Deoxyhypusine synthase catalyzes the formation of a deoxyhypusine by transferring an aminobutyl moiety from spermidine onto a conserved lysine residue within the eIF5A.
-xref: record_id "1041"
-xref: delta_mono_mass "71.073499"
-xref: delta_avge_mass "71.121"
-xref: delta_composition "H(9) C(4) N"
-xref: username_of_poster "cbarrero"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-15 12:04:35"
-xref: date_time_modified "2024-08-12 10:11:43"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "Q"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_2_misc_notes "putrescine Q-PUT"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1042
-name: Acetyldeoxyhypusine
-def: "Acetyldeoxyhypusine." [PMID:20942800, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1042]
-comment: Regulation of eIF5A by deoxyhypusine acetylation/deacetylation.
-xref: record_id "1042"
-xref: delta_mono_mass "113.084064"
-xref: delta_avge_mass "113.1576"
-xref: delta_composition "H(11) C(6) N O"
-xref: username_of_poster "cbarrero"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-18 04:14:19"
-xref: date_time_modified "2021-07-06 14:44:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1043
-name: Acetylhypusine
-def: "Acetylhypusine." [PMID:20942800, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1043]
-comment: Regulation of eIF5A by hypusine acetylation/deacetylation.
-xref: record_id "1043"
-xref: delta_mono_mass "129.078979"
-xref: delta_avge_mass "129.157"
-xref: delta_composition "H(11) C(6) N O(2)"
-xref: username_of_poster "cbarrero"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-18 04:16:59"
-xref: date_time_modified "2021-07-06 14:44:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1044
-name: Ala->Cys
-def: "Ala->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1044]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1044"
-xref: delta_mono_mass "31.972071"
-xref: delta_avge_mass "32.065"
-xref: delta_composition "S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 16:49:30"
-xref: date_time_modified "2011-06-20 16:49:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1045
-name: Ala->Phe
-def: "Ala->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1045]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1045"
-xref: delta_mono_mass "76.0313"
-xref: delta_avge_mass "76.096"
-xref: delta_composition "H(4) C(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 16:50:25"
-xref: date_time_modified "2011-06-20 16:50:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1046
-name: Ala->His
-def: "Ala->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1046]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1046"
-xref: delta_mono_mass "66.021798"
-xref: delta_avge_mass "66.0614"
-xref: delta_composition "H(2) C(3) N(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 16:56:21"
-xref: date_time_modified "2011-06-20 16:56:21"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1047
-name: Ala->Xle
-def: "Ala->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1047]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1047"
-xref: delta_mono_mass "42.04695"
-xref: delta_avge_mass "42.0797"
-xref: delta_composition "H(6) C(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 16:57:10"
-xref: date_time_modified "2011-06-21 15:12:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1048
-name: Ala->Lys
-def: "Ala->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1048]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1048"
-xref: delta_mono_mass "57.057849"
-xref: delta_avge_mass "57.0944"
-xref: delta_composition "H(7) C(3) N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 16:57:37"
-xref: date_time_modified "2011-06-20 16:57:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1049
-name: Ala->Met
-def: "Ala->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1049]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1049"
-xref: delta_mono_mass "60.003371"
-xref: delta_avge_mass "60.1182"
-xref: delta_composition "H(4) C(2) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 16:58:05"
-xref: date_time_modified "2011-06-20 16:58:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1050
-name: Ala->Asn
-def: "Ala->Asn substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1050]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1050"
-xref: delta_mono_mass "43.005814"
-xref: delta_avge_mass "43.0247"
-xref: delta_composition "H C N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 16:58:32"
-xref: date_time_modified "2011-06-20 16:58:32"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1051
-name: Ala->Gln
-def: "Ala->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1051]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1051"
-xref: delta_mono_mass "57.021464"
-xref: delta_avge_mass "57.0513"
-xref: delta_composition "H(3) C(2) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 16:58:56"
-xref: date_time_modified "2011-06-20 16:58:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1052
-name: Ala->Arg
-def: "Ala->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1052]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1052"
-xref: delta_mono_mass "85.063997"
-xref: delta_avge_mass "85.1078"
-xref: delta_composition "H(7) C(3) N(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 16:59:22"
-xref: date_time_modified "2011-06-20 16:59:22"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1053
-name: Ala->Trp
-def: "Ala->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1053]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1053"
-xref: delta_mono_mass "115.042199"
-xref: delta_avge_mass "115.132"
-xref: delta_composition "H(5) C(8) N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 16:59:45"
-xref: date_time_modified "2011-06-20 16:59:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1054
-name: Ala->Tyr
-def: "Ala->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1054]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1054"
-xref: delta_mono_mass "92.026215"
-xref: delta_avge_mass "92.0954"
-xref: delta_composition "H(4) C(6) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:00:09"
-xref: date_time_modified "2011-06-20 17:00:09"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1055
-name: Cys->Ala
-def: "Cys->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1055]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1055"
-xref: delta_mono_mass "-31.972071"
-xref: delta_avge_mass "-32.065"
-xref: delta_composition "S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:26:22"
-xref: date_time_modified "2011-06-20 17:26:22"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1056
-name: Cys->Asp
-def: "Cys->Asp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1056]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1056"
-xref: delta_mono_mass "12.017759"
-xref: delta_avge_mass "11.9445"
-xref: delta_composition "C O(2) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:26:57"
-xref: date_time_modified "2011-06-20 17:26:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1057
-name: Cys->Glu
-def: "Cys->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1057]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1057"
-xref: delta_mono_mass "26.033409"
-xref: delta_avge_mass "25.9711"
-xref: delta_composition "H(2) C(2) O(2) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:27:25"
-xref: date_time_modified "2011-06-20 17:27:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1058
-name: Cys->His
-def: "Cys->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1058]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1058"
-xref: delta_mono_mass "34.049727"
-xref: delta_avge_mass "33.9964"
-xref: delta_composition "H(2) C(3) N(2) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:27:48"
-xref: date_time_modified "2011-06-20 17:27:48"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1059
-name: Cys->Xle
-def: "Cys->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1059]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1059"
-xref: delta_mono_mass "10.07488"
-xref: delta_avge_mass "10.0147"
-xref: delta_composition "H(6) C(3) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:28:11"
-xref: date_time_modified "2011-06-21 15:14:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1060
-name: Cys->Lys
-def: "Cys->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1060]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1060"
-xref: delta_mono_mass "25.085779"
-xref: delta_avge_mass "25.0294"
-xref: delta_composition "H(7) C(3) N S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:28:36"
-xref: date_time_modified "2011-06-20 17:28:36"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1061
-name: Cys->Met
-def: "Cys->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1061]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1061"
-xref: delta_mono_mass "28.0313"
-xref: delta_avge_mass "28.0532"
-xref: delta_composition "H(4) C(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:29:04"
-xref: date_time_modified "2011-06-20 17:29:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1062
-name: Cys->Asn
-def: "Cys->Asn substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1062]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1062"
-xref: delta_mono_mass "11.033743"
-xref: delta_avge_mass "10.9597"
-xref: delta_composition "H C N O S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:29:28"
-xref: date_time_modified "2011-06-20 17:29:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1063
-name: Cys->Pro
-def: "Cys->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1063]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1063"
-xref: delta_mono_mass "-5.956421"
-xref: delta_avge_mass "-6.0277"
-xref: delta_composition "H(2) C(2) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:29:55"
-xref: date_time_modified "2011-06-20 17:29:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1064
-name: Cys->Gln
-def: "Cys->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1064]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1064"
-xref: delta_mono_mass "25.049393"
-xref: delta_avge_mass "24.9863"
-xref: delta_composition "H(3) C(2) N O S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:30:19"
-xref: date_time_modified "2011-06-20 17:30:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1065
-name: Cys->Thr
-def: "Cys->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1065]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1065"
-xref: delta_mono_mass "-1.961506"
-xref: delta_avge_mass "-2.039"
-xref: delta_composition "H(2) C O S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:30:53"
-xref: date_time_modified "2011-06-20 17:30:53"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1066
-name: Cys->Val
-def: "Cys->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1066]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1066"
-xref: delta_mono_mass "-3.940771"
-xref: delta_avge_mass "-4.0118"
-xref: delta_composition "H(4) C(2) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:31:23"
-xref: date_time_modified "2011-06-20 17:31:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1067
-name: Asp->Cys
-def: "Asp->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1067]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1067"
-xref: delta_mono_mass "-12.017759"
-xref: delta_avge_mass "-11.9445"
-xref: delta_composition "C(-1) O(-2) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:40:11"
-xref: date_time_modified "2011-06-20 17:40:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1068
-name: Asp->Phe
-def: "Asp->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1068]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1068"
-xref: delta_mono_mass "32.041471"
-xref: delta_avge_mass "32.0865"
-xref: delta_composition "H(4) C(5) O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:40:35"
-xref: date_time_modified "2011-06-20 17:40:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1069
-name: Asp->Xle
-def: "Asp->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1069]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1069"
-xref: delta_mono_mass "-1.942879"
-xref: delta_avge_mass "-1.9298"
-xref: delta_composition "H(6) C(2) O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:41:00"
-xref: date_time_modified "2011-06-21 15:14:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1070
-name: Asp->Lys
-def: "Asp->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1070]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1070"
-xref: delta_mono_mass "13.06802"
-xref: delta_avge_mass "13.0849"
-xref: delta_composition "H(7) C(2) N O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:41:26"
-xref: date_time_modified "2011-06-20 17:41:26"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1071
-name: Asp->Met
-def: "Asp->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1071]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1071"
-xref: delta_mono_mass "16.013542"
-xref: delta_avge_mass "16.1087"
-xref: delta_composition "H(4) C O(-2) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:41:51"
-xref: date_time_modified "2011-06-20 17:41:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1072
-name: Asp->Pro
-def: "Asp->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1072]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1072"
-xref: delta_mono_mass "-17.974179"
-xref: delta_avge_mass "-17.9722"
-xref: delta_composition "H(2) C O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:42:17"
-xref: date_time_modified "2011-06-20 17:42:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1073
-name: Asp->Gln
-def: "Asp->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1073]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1073"
-xref: delta_mono_mass "13.031634"
-xref: delta_avge_mass "13.0418"
-xref: delta_composition "H(3) C N O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:42:41"
-xref: date_time_modified "2011-06-20 17:42:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1074
-name: Asp->Arg
-def: "Asp->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1074]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1074"
-xref: delta_mono_mass "41.074168"
-xref: delta_avge_mass "41.0983"
-xref: delta_composition "H(7) C(2) N(3) O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:43:03"
-xref: date_time_modified "2011-06-20 17:43:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1075
-name: Asp->Ser
-def: "Asp->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1075]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1075"
-xref: delta_mono_mass "-27.994915"
-xref: delta_avge_mass "-28.0101"
-xref: delta_composition "C(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:43:25"
-xref: date_time_modified "2011-06-20 17:43:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1076
-name: Asp->Thr
-def: "Asp->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1076]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1076"
-xref: delta_mono_mass "-13.979265"
-xref: delta_avge_mass "-13.9835"
-xref: delta_composition "H(2) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:43:51"
-xref: date_time_modified "2011-06-20 17:43:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1077
-name: Asp->Trp
-def: "Asp->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1077]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1077"
-xref: delta_mono_mass "71.05237"
-xref: delta_avge_mass "71.1225"
-xref: delta_composition "H(5) C(7) N O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:44:16"
-xref: date_time_modified "2011-06-20 17:44:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1078
-name: Glu->Cys
-def: "Glu->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1078]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1078"
-xref: delta_mono_mass "-26.033409"
-xref: delta_avge_mass "-25.9711"
-xref: delta_composition "H(-2) C(-2) O(-2) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 12:00:46"
-xref: date_time_modified "2011-06-21 12:00:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1079
-name: Glu->Phe
-def: "Glu->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1079]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1079"
-xref: delta_mono_mass "18.025821"
-xref: delta_avge_mass "18.0599"
-xref: delta_composition "H(2) C(4) O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 12:01:12"
-xref: date_time_modified "2011-06-21 12:01:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1080
-name: Glu->His
-def: "Glu->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1080]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1080"
-xref: delta_mono_mass "8.016319"
-xref: delta_avge_mass "8.0253"
-xref: delta_composition "C N(2) O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 12:01:42"
-xref: date_time_modified "2011-06-21 12:01:42"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1081
-name: Glu->Xle
-def: "Glu->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1081]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1081"
-xref: delta_mono_mass "-15.958529"
-xref: delta_avge_mass "-15.9563"
-xref: delta_composition "H(4) C O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 12:02:09"
-xref: date_time_modified "2011-06-21 15:15:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1082
-name: Glu->Met
-def: "Glu->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1082]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1082"
-xref: delta_mono_mass "1.997892"
-xref: delta_avge_mass "2.0821"
-xref: delta_composition "H(2) O(-2) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 12:02:35"
-xref: date_time_modified "2011-06-21 12:02:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1083
-name: Glu->Asn
-def: "Glu->Asn substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1083]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1083"
-xref: delta_mono_mass "-14.999666"
-xref: delta_avge_mass "-15.0113"
-xref: delta_composition "H(-1) C(-1) N O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 12:03:01"
-xref: date_time_modified "2011-06-21 12:03:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1084
-name: Glu->Pro
-def: "Glu->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1084]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1084"
-xref: delta_mono_mass "-31.989829"
-xref: delta_avge_mass "-31.9988"
-xref: delta_composition "O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 12:03:25"
-xref: date_time_modified "2011-06-21 12:03:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1085
-name: Glu->Arg
-def: "Glu->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1085]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1085"
-xref: delta_mono_mass "27.058518"
-xref: delta_avge_mass "27.0717"
-xref: delta_composition "H(5) C N(3) O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 12:03:48"
-xref: date_time_modified "2011-06-21 12:03:48"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1086
-name: Glu->Ser
-def: "Glu->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1086]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1086"
-xref: delta_mono_mass "-42.010565"
-xref: delta_avge_mass "-42.0367"
-xref: delta_composition "H(-2) C(-2) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 12:04:12"
-xref: date_time_modified "2011-06-21 12:04:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1087
-name: Glu->Thr
-def: "Glu->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1087]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1087"
-xref: delta_mono_mass "-27.994915"
-xref: delta_avge_mass "-28.0101"
-xref: delta_composition "C(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 12:04:38"
-xref: date_time_modified "2011-06-21 12:04:38"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1088
-name: Glu->Trp
-def: "Glu->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1088]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1088"
-xref: delta_mono_mass "57.03672"
-xref: delta_avge_mass "57.0959"
-xref: delta_composition "H(3) C(6) N O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 12:05:01"
-xref: date_time_modified "2011-06-21 12:05:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1089
-name: Glu->Tyr
-def: "Glu->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1089]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1089"
-xref: delta_mono_mass "34.020735"
-xref: delta_avge_mass "34.0593"
-xref: delta_composition "H(2) C(4) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 12:05:23"
-xref: date_time_modified "2011-06-21 12:05:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1090
-name: Phe->Ala
-def: "Phe->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1090]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1090"
-xref: delta_mono_mass "-76.0313"
-xref: delta_avge_mass "-76.096"
-xref: delta_composition "H(-4) C(-6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 13:41:15"
-xref: date_time_modified "2011-06-21 13:41:15"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1091
-name: Phe->Asp
-def: "Phe->Asp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1091]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1091"
-xref: delta_mono_mass "-32.041471"
-xref: delta_avge_mass "-32.0865"
-xref: delta_composition "H(-4) C(-5) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 13:41:48"
-xref: date_time_modified "2011-06-21 13:41:48"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1092
-name: Phe->Glu
-def: "Phe->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1092]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1092"
-xref: delta_mono_mass "-18.025821"
-xref: delta_avge_mass "-18.0599"
-xref: delta_composition "H(-2) C(-4) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 13:56:57"
-xref: date_time_modified "2011-06-21 13:56:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1093
-name: Phe->Gly
-def: "Phe->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1093]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1093"
-xref: delta_mono_mass "-90.04695"
-xref: delta_avge_mass "-90.1225"
-xref: delta_composition "H(-6) C(-7)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 13:57:23"
-xref: date_time_modified "2011-06-21 13:57:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1094
-name: Phe->His
-def: "Phe->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1094]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1094"
-xref: delta_mono_mass "-10.009502"
-xref: delta_avge_mass "-10.0346"
-xref: delta_composition "H(-2) C(-3) N(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 13:57:45"
-xref: date_time_modified "2011-06-21 13:57:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1095
-name: Phe->Lys
-def: "Phe->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1095]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1095"
-xref: delta_mono_mass "-18.973451"
-xref: delta_avge_mass "-19.0016"
-xref: delta_composition "H(3) C(-3) N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 13:58:10"
-xref: date_time_modified "2011-06-21 13:58:10"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1096
-name: Phe->Met
-def: "Phe->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1096]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1096"
-xref: delta_mono_mass "-16.027929"
-xref: delta_avge_mass "-15.9778"
-xref: delta_composition "C(-4) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 13:58:32"
-xref: date_time_modified "2011-06-21 13:58:32"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1097
-name: Phe->Asn
-def: "Phe->Asn substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1097]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1097"
-xref: delta_mono_mass "-33.025486"
-xref: delta_avge_mass "-33.0712"
-xref: delta_composition "H(-3) C(-5) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 13:58:57"
-xref: date_time_modified "2011-06-21 13:58:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1098
-name: Phe->Pro
-def: "Phe->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1098]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1098"
-xref: delta_mono_mass "-50.01565"
-xref: delta_avge_mass "-50.0587"
-xref: delta_composition "H(-2) C(-4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 13:59:19"
-xref: date_time_modified "2011-06-21 13:59:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1099
-name: Phe->Gln
-def: "Phe->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1099]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1099"
-xref: delta_mono_mass "-19.009836"
-xref: delta_avge_mass "-19.0446"
-xref: delta_composition "H(-1) C(-4) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 13:59:42"
-xref: date_time_modified "2011-06-21 13:59:42"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1100
-name: Phe->Arg
-def: "Phe->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1100]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1100"
-xref: delta_mono_mass "9.032697"
-xref: delta_avge_mass "9.0118"
-xref: delta_composition "H(3) C(-3) N(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:00:05"
-xref: date_time_modified "2011-06-21 14:00:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1101
-name: Phe->Thr
-def: "Phe->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1101]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1101"
-xref: delta_mono_mass "-46.020735"
-xref: delta_avge_mass "-46.07"
-xref: delta_composition "H(-2) C(-5) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:00:30"
-xref: date_time_modified "2011-06-21 14:00:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1102
-name: Phe->Trp
-def: "Phe->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1102]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1102"
-xref: delta_mono_mass "39.010899"
-xref: delta_avge_mass "39.036"
-xref: delta_composition "H C(2) N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:00:53"
-xref: date_time_modified "2011-06-21 14:00:53"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1103
-name: Gly->Phe
-def: "Gly->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1103]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1103"
-xref: delta_mono_mass "90.04695"
-xref: delta_avge_mass "90.1225"
-xref: delta_composition "H(6) C(7)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:03:41"
-xref: date_time_modified "2011-06-21 14:03:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1104
-name: Gly->His
-def: "Gly->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1104]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1104"
-xref: delta_mono_mass "80.037448"
-xref: delta_avge_mass "80.088"
-xref: delta_composition "H(4) C(4) N(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:04:05"
-xref: date_time_modified "2011-06-21 14:04:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1105
-name: Gly->Xle
-def: "Gly->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1105]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1105"
-xref: delta_mono_mass "56.0626"
-xref: delta_avge_mass "56.1063"
-xref: delta_composition "H(8) C(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:04:27"
-xref: date_time_modified "2011-06-21 15:15:58"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1106
-name: Gly->Lys
-def: "Gly->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1106]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1106"
-xref: delta_mono_mass "71.073499"
-xref: delta_avge_mass "71.121"
-xref: delta_composition "H(9) C(4) N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:04:51"
-xref: date_time_modified "2011-06-21 14:04:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1107
-name: Gly->Met
-def: "Gly->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1107]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1107"
-xref: delta_mono_mass "74.019021"
-xref: delta_avge_mass "74.1447"
-xref: delta_composition "H(6) C(3) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:05:16"
-xref: date_time_modified "2011-06-21 14:05:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1108
-name: Gly->Asn
-def: "Gly->Asn substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1108]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1108"
-xref: delta_mono_mass "57.021464"
-xref: delta_avge_mass "57.0513"
-xref: delta_composition "H(3) C(2) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:05:35"
-xref: date_time_modified "2011-06-21 14:05:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1109
-name: Gly->Pro
-def: "Gly->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1109]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1109"
-xref: delta_mono_mass "40.0313"
-xref: delta_avge_mass "40.0639"
-xref: delta_composition "H(4) C(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:05:55"
-xref: date_time_modified "2011-06-21 14:05:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1110
-name: Gly->Gln
-def: "Gly->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1110]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1110"
-xref: delta_mono_mass "71.037114"
-xref: delta_avge_mass "71.0779"
-xref: delta_composition "H(5) C(3) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:06:16"
-xref: date_time_modified "2011-06-21 14:06:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1111
-name: Gly->Thr
-def: "Gly->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1111]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1111"
-xref: delta_mono_mass "44.026215"
-xref: delta_avge_mass "44.0526"
-xref: delta_composition "H(4) C(2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:06:40"
-xref: date_time_modified "2011-06-21 14:06:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1112
-name: Gly->Tyr
-def: "Gly->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1112]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1112"
-xref: delta_mono_mass "106.041865"
-xref: delta_avge_mass "106.1219"
-xref: delta_composition "H(6) C(7) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:07:05"
-xref: date_time_modified "2011-06-21 14:07:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1113
-name: His->Ala
-def: "His->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1113]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1113"
-xref: delta_mono_mass "-66.021798"
-xref: delta_avge_mass "-66.0614"
-xref: delta_composition "H(-2) C(-3) N(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:51:31"
-xref: date_time_modified "2011-06-21 14:51:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1114
-name: His->Cys
-def: "His->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1114]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1114"
-xref: delta_mono_mass "-34.049727"
-xref: delta_avge_mass "-33.9964"
-xref: delta_composition "H(-2) C(-3) N(-2) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:51:56"
-xref: date_time_modified "2011-06-21 14:51:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1115
-name: His->Glu
-def: "His->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1115]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1115"
-xref: delta_mono_mass "-8.016319"
-xref: delta_avge_mass "-8.0253"
-xref: delta_composition "C(-1) N(-2) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:52:16"
-xref: date_time_modified "2011-06-21 14:52:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1116
-name: His->Phe
-def: "His->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1116]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1116"
-xref: delta_mono_mass "10.009502"
-xref: delta_avge_mass "10.0346"
-xref: delta_composition "H(2) C(3) N(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:52:50"
-xref: date_time_modified "2011-06-21 14:52:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1117
-name: His->Gly
-def: "His->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1117]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1117"
-xref: delta_mono_mass "-80.037448"
-xref: delta_avge_mass "-80.088"
-xref: delta_composition "H(-4) C(-4) N(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:53:45"
-xref: date_time_modified "2011-06-21 14:53:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1119
-name: His->Lys
-def: "His->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1119]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1119"
-xref: delta_mono_mass "-8.963949"
-xref: delta_avge_mass "-8.967"
-xref: delta_composition "H(5) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:59:08"
-xref: date_time_modified "2011-06-21 14:59:08"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1120
-name: His->Met
-def: "His->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1120]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1120"
-xref: delta_mono_mass "-6.018427"
-xref: delta_avge_mass "-5.9432"
-xref: delta_composition "H(2) C(-1) N(-2) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:59:30"
-xref: date_time_modified "2011-06-21 14:59:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1121
-name: His->Ser
-def: "His->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1121]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1121"
-xref: delta_mono_mass "-50.026883"
-xref: delta_avge_mass "-50.062"
-xref: delta_composition "H(-2) C(-3) N(-2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:59:50"
-xref: date_time_modified "2011-06-21 14:59:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1122
-name: His->Thr
-def: "His->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1122]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1122"
-xref: delta_mono_mass "-36.011233"
-xref: delta_avge_mass "-36.0354"
-xref: delta_composition "C(-2) N(-2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 15:00:20"
-xref: date_time_modified "2011-06-21 15:00:20"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1123
-name: His->Val
-def: "His->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1123]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1123"
-xref: delta_mono_mass "-37.990498"
-xref: delta_avge_mass "-38.0082"
-xref: delta_composition "H(2) C(-1) N(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 15:00:41"
-xref: date_time_modified "2011-06-21 15:00:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1124
-name: His->Trp
-def: "His->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1124]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1124"
-xref: delta_mono_mass "49.020401"
-xref: delta_avge_mass "49.0706"
-xref: delta_composition "H(3) C(5) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 15:01:02"
-xref: date_time_modified "2011-06-21 15:01:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1125
-name: Xle->Ala
-def: "Leu/Ile->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1125]
-xref: record_id "1125"
-xref: delta_mono_mass "-42.04695"
-xref: delta_avge_mass "-42.0797"
-xref: delta_composition "H(-6) C(-3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 15:33:19"
-xref: date_time_modified "2011-06-21 15:33:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "I"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1126
-name: Xle->Cys
-def: "Leu/Ile->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1126]
-xref: record_id "1126"
-xref: delta_mono_mass "-10.07488"
-xref: delta_avge_mass "-10.0147"
-xref: delta_composition "H(-6) C(-3) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 15:33:43"
-xref: date_time_modified "2011-06-21 15:33:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "I"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1127
-name: Xle->Asp
-def: "Leu/Ile->Asp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1127]
-xref: record_id "1127"
-xref: delta_mono_mass "1.942879"
-xref: delta_avge_mass "1.9298"
-xref: delta_composition "H(-6) C(-2) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 15:34:14"
-xref: date_time_modified "2011-06-21 15:34:14"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "I"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1128
-name: Xle->Glu
-def: "Leu/Ile->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1128]
-xref: record_id "1128"
-xref: delta_mono_mass "15.958529"
-xref: delta_avge_mass "15.9563"
-xref: delta_composition "H(-4) C(-1) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 15:34:40"
-xref: date_time_modified "2011-06-21 15:34:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "I"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1129
-name: Xle->Gly
-def: "Leu/Ile->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1129]
-xref: record_id "1129"
-xref: delta_mono_mass "-56.0626"
-xref: delta_avge_mass "-56.1063"
-xref: delta_composition "H(-8) C(-4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 15:35:12"
-xref: date_time_modified "2011-06-21 15:35:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "I"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1130
-name: Xle->Tyr
-def: "Leu/Ile->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1130]
-xref: record_id "1130"
-xref: delta_mono_mass "49.979265"
-xref: delta_avge_mass "50.0156"
-xref: delta_composition "H(-2) C(3) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 15:35:36"
-xref: date_time_modified "2011-06-21 15:35:36"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "I"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1131
-name: Lys->Ala
-def: "Lys->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1131]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1131"
-xref: delta_mono_mass "-57.057849"
-xref: delta_avge_mass "-57.0944"
-xref: delta_composition "H(-7) C(-3) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 15:37:25"
-xref: date_time_modified "2011-06-21 15:37:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1132
-name: Lys->Cys
-def: "Lys->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1132]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1132"
-xref: delta_mono_mass "-25.085779"
-xref: delta_avge_mass "-25.0294"
-xref: delta_composition "H(-7) C(-3) N(-1) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:01:01"
-xref: date_time_modified "2011-06-21 16:01:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1133
-name: Lys->Asp
-def: "Lys->Asp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1133]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1133"
-xref: delta_mono_mass "-13.06802"
-xref: delta_avge_mass "-13.0849"
-xref: delta_composition "H(-7) C(-2) N(-1) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:01:33"
-xref: date_time_modified "2011-06-21 16:01:33"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1134
-name: Lys->Phe
-def: "Lys->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1134]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1134"
-xref: delta_mono_mass "18.973451"
-xref: delta_avge_mass "19.0016"
-xref: delta_composition "H(-3) C(3) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:01:56"
-xref: date_time_modified "2011-06-21 16:01:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1135
-name: Lys->Gly
-def: "Lys->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1135]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1135"
-xref: delta_mono_mass "-71.073499"
-xref: delta_avge_mass "-71.121"
-xref: delta_composition "H(-9) C(-4) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:02:20"
-xref: date_time_modified "2011-06-21 16:02:20"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1136
-name: Lys->His
-def: "Lys->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1136]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1136"
-xref: delta_mono_mass "8.963949"
-xref: delta_avge_mass "8.967"
-xref: delta_composition "H(-5) N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:02:42"
-xref: date_time_modified "2011-06-21 16:02:42"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1137
-name: Lys->Pro
-def: "Lys->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1137]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1137"
-xref: delta_mono_mass "-31.042199"
-xref: delta_avge_mass "-31.0571"
-xref: delta_composition "H(-5) C(-1) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:03:06"
-xref: date_time_modified "2011-06-21 16:03:06"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1138
-name: Lys->Ser
-def: "Lys->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1138]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1138"
-xref: delta_mono_mass "-41.062935"
-xref: delta_avge_mass "-41.095"
-xref: delta_composition "H(-7) C(-3) N(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:03:27"
-xref: date_time_modified "2011-06-21 16:03:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1139
-name: Lys->Val
-def: "Lys->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1139]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1139"
-xref: delta_mono_mass "-29.026549"
-xref: delta_avge_mass "-29.0412"
-xref: delta_composition "H(-3) C(-1) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:03:49"
-xref: date_time_modified "2011-06-21 16:03:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1140
-name: Lys->Trp
-def: "Lys->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1140]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1140"
-xref: delta_mono_mass "57.98435"
-xref: delta_avge_mass "58.0376"
-xref: delta_composition "H(-2) C(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:04:11"
-xref: date_time_modified "2011-06-21 16:04:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1141
-name: Lys->Tyr
-def: "Lys->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1141]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1141"
-xref: delta_mono_mass "34.968366"
-xref: delta_avge_mass "35.001"
-xref: delta_composition "H(-3) C(3) N(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:04:35"
-xref: date_time_modified "2011-06-21 16:04:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1142
-name: Met->Ala
-def: "Met->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1142]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1142"
-xref: delta_mono_mass "-60.003371"
-xref: delta_avge_mass "-60.1182"
-xref: delta_composition "H(-4) C(-2) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:28:27"
-xref: date_time_modified "2011-06-21 16:28:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1143
-name: Met->Cys
-def: "Met->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1143]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1143"
-xref: delta_mono_mass "-28.0313"
-xref: delta_avge_mass "-28.0532"
-xref: delta_composition "H(-4) C(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:28:53"
-xref: date_time_modified "2011-06-21 16:28:53"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1144
-name: Met->Asp
-def: "Met->Asp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1144]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1144"
-xref: delta_mono_mass "-16.013542"
-xref: delta_avge_mass "-16.1087"
-xref: delta_composition "H(-4) C(-1) O(2) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:29:13"
-xref: date_time_modified "2011-06-21 16:29:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1145
-name: Met->Glu
-def: "Met->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1145]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1145"
-xref: delta_mono_mass "-1.997892"
-xref: delta_avge_mass "-2.0821"
-xref: delta_composition "H(-2) O(2) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:29:35"
-xref: date_time_modified "2011-06-21 16:29:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1146
-name: Met->Phe
-def: "Met->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1146]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1146"
-xref: delta_mono_mass "16.027929"
-xref: delta_avge_mass "15.9778"
-xref: delta_composition "C(4) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:30:07"
-xref: date_time_modified "2011-06-21 16:30:07"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1147
-name: Met->Gly
-def: "Met->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1147]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1147"
-xref: delta_mono_mass "-74.019021"
-xref: delta_avge_mass "-74.1447"
-xref: delta_composition "H(-6) C(-3) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:30:29"
-xref: date_time_modified "2011-06-21 16:30:29"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1148
-name: Met->His
-def: "Met->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1148]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1148"
-xref: delta_mono_mass "6.018427"
-xref: delta_avge_mass "5.9432"
-xref: delta_composition "H(-2) C N(2) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:30:50"
-xref: date_time_modified "2011-06-21 16:30:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1149
-name: Met->Asn
-def: "Met->Asn substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1149]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1149"
-xref: delta_mono_mass "-16.997557"
-xref: delta_avge_mass "-17.0934"
-xref: delta_composition "H(-3) C(-1) N O S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:31:14"
-xref: date_time_modified "2011-06-21 16:31:14"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1150
-name: Met->Pro
-def: "Met->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1150]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1150"
-xref: delta_mono_mass "-33.987721"
-xref: delta_avge_mass "-34.0809"
-xref: delta_composition "H(-2) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:31:34"
-xref: date_time_modified "2011-06-21 16:31:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1151
-name: Met->Gln
-def: "Met->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1151]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1151"
-xref: delta_mono_mass "-2.981907"
-xref: delta_avge_mass "-3.0668"
-xref: delta_composition "H(-1) N O S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:31:55"
-xref: date_time_modified "2011-06-21 16:31:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1152
-name: Met->Ser
-def: "Met->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1152]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1152"
-xref: delta_mono_mass "-44.008456"
-xref: delta_avge_mass "-44.1188"
-xref: delta_composition "H(-4) C(-2) O S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:32:16"
-xref: date_time_modified "2011-06-21 16:32:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1153
-name: Met->Trp
-def: "Met->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1153]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1153"
-xref: delta_mono_mass "55.038828"
-xref: delta_avge_mass "55.0138"
-xref: delta_composition "H C(6) N S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:32:38"
-xref: date_time_modified "2011-06-21 16:32:38"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1154
-name: Met->Tyr
-def: "Met->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1154]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1154"
-xref: delta_mono_mass "32.022844"
-xref: delta_avge_mass "31.9772"
-xref: delta_composition "C(4) O S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:33:00"
-xref: date_time_modified "2011-06-21 16:33:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1155
-name: Asn->Ala
-def: "Asn->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1155]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1155"
-xref: delta_mono_mass "-43.005814"
-xref: delta_avge_mass "-43.0247"
-xref: delta_composition "H(-1) C(-1) N(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:36:38"
-xref: date_time_modified "2011-06-21 16:36:38"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1156
-name: Asn->Cys
-def: "Asn->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1156]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1156"
-xref: delta_mono_mass "-11.033743"
-xref: delta_avge_mass "-10.9597"
-xref: delta_composition "H(-1) C(-1) N(-1) O(-1) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:37:03"
-xref: date_time_modified "2011-06-21 16:37:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1157
-name: Asn->Glu
-def: "Asn->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1157]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1157"
-xref: delta_mono_mass "14.999666"
-xref: delta_avge_mass "15.0113"
-xref: delta_composition "H C N(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:37:26"
-xref: date_time_modified "2011-06-21 16:37:26"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1158
-name: Asn->Phe
-def: "Asn->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1158]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1158"
-xref: delta_mono_mass "33.025486"
-xref: delta_avge_mass "33.0712"
-xref: delta_composition "H(3) C(5) N(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:37:48"
-xref: date_time_modified "2011-06-21 16:37:48"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1159
-name: Asn->Gly
-def: "Asn->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1159]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1159"
-xref: delta_mono_mass "-57.021464"
-xref: delta_avge_mass "-57.0513"
-xref: delta_composition "H(-3) C(-2) N(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:38:11"
-xref: date_time_modified "2011-06-21 16:38:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1160
-name: Asn->Met
-def: "Asn->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1160]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1160"
-xref: delta_mono_mass "16.997557"
-xref: delta_avge_mass "17.0934"
-xref: delta_composition "H(3) C N(-1) O(-1) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:38:32"
-xref: date_time_modified "2011-06-21 16:38:32"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1161
-name: Asn->Pro
-def: "Asn->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1161]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1161"
-xref: delta_mono_mass "-16.990164"
-xref: delta_avge_mass "-16.9875"
-xref: delta_composition "H C N(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:38:54"
-xref: date_time_modified "2011-06-21 16:38:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1162
-name: Asn->Gln
-def: "Asn->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1162]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1162"
-xref: delta_mono_mass "14.01565"
-xref: delta_avge_mass "14.0266"
-xref: delta_composition "H(2) C"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:39:15"
-xref: date_time_modified "2011-06-21 16:39:15"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1163
-name: Asn->Arg
-def: "Asn->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1163]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1163"
-xref: delta_mono_mass "42.058184"
-xref: delta_avge_mass "42.083"
-xref: delta_composition "H(6) C(2) N(2) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:39:37"
-xref: date_time_modified "2011-06-21 16:39:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1164
-name: Asn->Val
-def: "Asn->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1164]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1164"
-xref: delta_mono_mass "-14.974514"
-xref: delta_avge_mass "-14.9716"
-xref: delta_composition "H(3) C N(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:39:59"
-xref: date_time_modified "2011-06-21 16:39:59"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1165
-name: Asn->Trp
-def: "Asn->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1165]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1165"
-xref: delta_mono_mass "72.036386"
-xref: delta_avge_mass "72.1073"
-xref: delta_composition "H(4) C(7) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:40:21"
-xref: date_time_modified "2011-06-21 16:40:21"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1166
-name: Pro->Cys
-def: "Pro->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1166]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1166"
-xref: delta_mono_mass "5.956421"
-xref: delta_avge_mass "6.0277"
-xref: delta_composition "H(-2) C(-2) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:59:55"
-xref: date_time_modified "2011-06-21 16:59:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1167
-name: Pro->Asp
-def: "Pro->Asp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1167]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1167"
-xref: delta_mono_mass "17.974179"
-xref: delta_avge_mass "17.9722"
-xref: delta_composition "H(-2) C(-1) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:00:24"
-xref: date_time_modified "2011-06-21 17:00:24"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1168
-name: Pro->Glu
-def: "Pro->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1168]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1168"
-xref: delta_mono_mass "31.989829"
-xref: delta_avge_mass "31.9988"
-xref: delta_composition "O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:26:36"
-xref: date_time_modified "2011-06-21 17:26:36"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1169
-name: Pro->Phe
-def: "Pro->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1169]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1169"
-xref: delta_mono_mass "50.01565"
-xref: delta_avge_mass "50.0587"
-xref: delta_composition "H(2) C(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:26:56"
-xref: date_time_modified "2011-06-21 17:26:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1170
-name: Pro->Gly
-def: "Pro->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1170]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1170"
-xref: delta_mono_mass "-40.0313"
-xref: delta_avge_mass "-40.0639"
-xref: delta_composition "H(-4) C(-3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:27:17"
-xref: date_time_modified "2011-06-21 17:27:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1171
-name: Pro->Lys
-def: "Pro->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1171]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1171"
-xref: delta_mono_mass "31.042199"
-xref: delta_avge_mass "31.0571"
-xref: delta_composition "H(5) C N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:27:38"
-xref: date_time_modified "2011-06-21 17:27:38"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1172
-name: Pro->Met
-def: "Pro->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1172]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1172"
-xref: delta_mono_mass "33.987721"
-xref: delta_avge_mass "34.0809"
-xref: delta_composition "H(2) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:27:57"
-xref: date_time_modified "2011-06-21 17:27:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1173
-name: Pro->Asn
-def: "Pro->Asn substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1173]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1173"
-xref: delta_mono_mass "16.990164"
-xref: delta_avge_mass "16.9875"
-xref: delta_composition "H(-1) C(-1) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:28:18"
-xref: date_time_modified "2011-06-21 17:28:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1174
-name: Pro->Val
-def: "Pro->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1174]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1174"
-xref: delta_mono_mass "2.01565"
-xref: delta_avge_mass "2.0159"
-xref: delta_composition "H(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:28:41"
-xref: date_time_modified "2011-06-21 17:28:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1175
-name: Pro->Trp
-def: "Pro->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1175]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1175"
-xref: delta_mono_mass "89.026549"
-xref: delta_avge_mass "89.0947"
-xref: delta_composition "H(3) C(6) N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:29:04"
-xref: date_time_modified "2011-06-21 17:29:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1176
-name: Pro->Tyr
-def: "Pro->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1176]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1176"
-xref: delta_mono_mass "66.010565"
-xref: delta_avge_mass "66.0581"
-xref: delta_composition "H(2) C(4) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:29:24"
-xref: date_time_modified "2011-06-21 17:29:24"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1177
-name: Gln->Ala
-def: "Gln->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1177]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1177"
-xref: delta_mono_mass "-57.021464"
-xref: delta_avge_mass "-57.0513"
-xref: delta_composition "H(-3) C(-2) N(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:39:52"
-xref: date_time_modified "2011-06-21 17:39:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1178
-name: Gln->Cys
-def: "Gln->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1178]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1178"
-xref: delta_mono_mass "-25.049393"
-xref: delta_avge_mass "-24.9863"
-xref: delta_composition "H(-3) C(-2) N(-1) O(-1) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:40:20"
-xref: date_time_modified "2011-06-21 17:40:20"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1179
-name: Gln->Asp
-def: "Gln->Asp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1179]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1179"
-xref: delta_mono_mass "-13.031634"
-xref: delta_avge_mass "-13.0418"
-xref: delta_composition "H(-3) C(-1) N(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:40:42"
-xref: date_time_modified "2011-06-21 17:40:42"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1180
-name: Gln->Phe
-def: "Gln->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1180]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1180"
-xref: delta_mono_mass "19.009836"
-xref: delta_avge_mass "19.0446"
-xref: delta_composition "H C(4) N(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:41:04"
-xref: date_time_modified "2011-06-21 17:41:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1181
-name: Gln->Gly
-def: "Gln->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1181]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1181"
-xref: delta_mono_mass "-71.037114"
-xref: delta_avge_mass "-71.0779"
-xref: delta_composition "H(-5) C(-3) N(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:41:24"
-xref: date_time_modified "2011-06-21 17:41:24"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1182
-name: Gln->Met
-def: "Gln->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1182]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1182"
-xref: delta_mono_mass "2.981907"
-xref: delta_avge_mass "3.0668"
-xref: delta_composition "H N(-1) O(-1) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:41:53"
-xref: date_time_modified "2011-06-21 17:41:53"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1183
-name: Gln->Asn
-def: "Gln->Asn substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1183]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1183"
-xref: delta_mono_mass "-14.01565"
-xref: delta_avge_mass "-14.0266"
-xref: delta_composition "H(-2) C(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:42:17"
-xref: date_time_modified "2011-06-21 17:42:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1184
-name: Gln->Ser
-def: "Gln->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1184]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1184"
-xref: delta_mono_mass "-41.026549"
-xref: delta_avge_mass "-41.0519"
-xref: delta_composition "H(-3) C(-2) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:42:37"
-xref: date_time_modified "2011-06-21 17:42:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1185
-name: Gln->Thr
-def: "Gln->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1185]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1185"
-xref: delta_mono_mass "-27.010899"
-xref: delta_avge_mass "-27.0253"
-xref: delta_composition "H(-1) C(-1) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:42:58"
-xref: date_time_modified "2011-06-21 17:42:58"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1186
-name: Gln->Val
-def: "Gln->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1186]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1186"
-xref: delta_mono_mass "-28.990164"
-xref: delta_avge_mass "-28.9982"
-xref: delta_composition "H N(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:43:20"
-xref: date_time_modified "2011-06-21 17:43:20"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1187
-name: Gln->Trp
-def: "Gln->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1187]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1187"
-xref: delta_mono_mass "58.020735"
-xref: delta_avge_mass "58.0807"
-xref: delta_composition "H(2) C(6) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:43:42"
-xref: date_time_modified "2011-06-21 17:43:42"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1188
-name: Gln->Tyr
-def: "Gln->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1188]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1188"
-xref: delta_mono_mass "35.004751"
-xref: delta_avge_mass "35.044"
-xref: delta_composition "H C(4) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:44:02"
-xref: date_time_modified "2011-06-21 17:44:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1189
-name: Arg->Ala
-def: "Arg->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1189]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1189"
-xref: delta_mono_mass "-85.063997"
-xref: delta_avge_mass "-85.1078"
-xref: delta_composition "H(-7) C(-3) N(-3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 10:47:36"
-xref: date_time_modified "2011-06-23 10:47:36"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1190
-name: Arg->Asp
-def: "Arg->Asp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1190]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1190"
-xref: delta_mono_mass "-41.074168"
-xref: delta_avge_mass "-41.0983"
-xref: delta_composition "H(-7) C(-2) N(-3) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 10:48:03"
-xref: date_time_modified "2011-06-23 10:48:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1191
-name: Arg->Glu
-def: "Arg->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1191]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1191"
-xref: delta_mono_mass "-27.058518"
-xref: delta_avge_mass "-27.0717"
-xref: delta_composition "H(-5) C(-1) N(-3) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 10:48:51"
-xref: date_time_modified "2011-06-23 10:48:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1192
-name: Arg->Asn
-def: "Arg->Asn substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1192]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1192"
-xref: delta_mono_mass "-42.058184"
-xref: delta_avge_mass "-42.083"
-xref: delta_composition "H(-6) C(-2) N(-2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 10:49:09"
-xref: date_time_modified "2011-06-23 10:49:29"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1193
-name: Arg->Val
-def: "Arg->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1193]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1193"
-xref: delta_mono_mass "-57.032697"
-xref: delta_avge_mass "-57.0546"
-xref: delta_composition "H(-3) C(-1) N(-3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 10:49:53"
-xref: date_time_modified "2011-06-23 10:49:53"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1194
-name: Arg->Tyr
-def: "Arg->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1194]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1194"
-xref: delta_mono_mass "6.962218"
-xref: delta_avge_mass "6.9876"
-xref: delta_composition "H(-3) C(3) N(-3) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 10:50:15"
-xref: date_time_modified "2011-06-23 10:50:15"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1195
-name: Arg->Phe
-def: "Arg->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1195]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1195"
-xref: delta_mono_mass "-9.032697"
-xref: delta_avge_mass "-9.0118"
-xref: delta_composition "H(-3) C(3) N(-3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 10:55:03"
-xref: date_time_modified "2011-06-23 10:55:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1196
-name: Ser->Asp
-def: "Ser->Asp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1196]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1196"
-xref: delta_mono_mass "27.994915"
-xref: delta_avge_mass "28.0101"
-xref: delta_composition "C O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 10:57:45"
-xref: date_time_modified "2011-06-23 10:57:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1197
-name: Ser->Glu
-def: "Ser->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1197]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1197"
-xref: delta_mono_mass "42.010565"
-xref: delta_avge_mass "42.0367"
-xref: delta_composition "H(2) C(2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 10:58:11"
-xref: date_time_modified "2011-06-23 10:58:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1198
-name: Ser->His
-def: "Ser->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1198]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1198"
-xref: delta_mono_mass "50.026883"
-xref: delta_avge_mass "50.062"
-xref: delta_composition "H(2) C(3) N(2) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 10:58:34"
-xref: date_time_modified "2011-06-23 10:58:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1199
-name: Ser->Lys
-def: "Ser->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1199]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1199"
-xref: delta_mono_mass "41.062935"
-xref: delta_avge_mass "41.095"
-xref: delta_composition "H(7) C(3) N O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 10:58:58"
-xref: date_time_modified "2011-06-23 10:58:58"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1200
-name: Ser->Met
-def: "Ser->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1200]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1200"
-xref: delta_mono_mass "44.008456"
-xref: delta_avge_mass "44.1188"
-xref: delta_composition "H(4) C(2) O(-1) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 10:59:19"
-xref: date_time_modified "2011-06-23 10:59:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1201
-name: Ser->Gln
-def: "Ser->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1201]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1201"
-xref: delta_mono_mass "41.026549"
-xref: delta_avge_mass "41.0519"
-xref: delta_composition "H(3) C(2) N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 10:59:38"
-xref: date_time_modified "2011-06-23 10:59:38"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1202
-name: Ser->Val
-def: "Ser->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1202]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1202"
-xref: delta_mono_mass "12.036386"
-xref: delta_avge_mass "12.0538"
-xref: delta_composition "H(4) C(2) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 10:59:59"
-xref: date_time_modified "2011-06-23 10:59:59"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1203
-name: Thr->Cys
-def: "Thr->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1203]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1203"
-xref: delta_mono_mass "1.961506"
-xref: delta_avge_mass "2.039"
-xref: delta_composition "H(-2) C(-1) O(-1) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:00:56"
-xref: date_time_modified "2011-06-23 11:00:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1204
-name: Thr->Asp
-def: "Thr->Asp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1204]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1204"
-xref: delta_mono_mass "13.979265"
-xref: delta_avge_mass "13.9835"
-xref: delta_composition "H(-2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:01:35"
-xref: date_time_modified "2011-06-23 11:01:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1205
-name: Thr->Glu
-def: "Thr->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1205]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1205"
-xref: delta_mono_mass "27.994915"
-xref: delta_avge_mass "28.0101"
-xref: delta_composition "C O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:02:00"
-xref: date_time_modified "2011-06-23 11:02:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1206
-name: Thr->Phe
-def: "Thr->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1206]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1206"
-xref: delta_mono_mass "46.020735"
-xref: delta_avge_mass "46.07"
-xref: delta_composition "H(2) C(5) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:02:21"
-xref: date_time_modified "2011-06-23 11:02:21"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1207
-name: Thr->Gly
-def: "Thr->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1207]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1207"
-xref: delta_mono_mass "-44.026215"
-xref: delta_avge_mass "-44.0526"
-xref: delta_composition "H(-4) C(-2) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:02:41"
-xref: date_time_modified "2011-06-23 11:02:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1208
-name: Thr->His
-def: "Thr->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1208]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1208"
-xref: delta_mono_mass "36.011233"
-xref: delta_avge_mass "36.0354"
-xref: delta_composition "C(2) N(2) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:03:03"
-xref: date_time_modified "2011-06-23 11:03:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1209
-name: Thr->Gln
-def: "Thr->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1209]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1209"
-xref: delta_mono_mass "27.010899"
-xref: delta_avge_mass "27.0253"
-xref: delta_composition "H C N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:03:26"
-xref: date_time_modified "2011-06-23 11:03:26"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1210
-name: Thr->Val
-def: "Thr->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1210]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1210"
-xref: delta_mono_mass "-1.979265"
-xref: delta_avge_mass "-1.9728"
-xref: delta_composition "H(2) C O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:03:48"
-xref: date_time_modified "2011-06-23 11:03:48"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1211
-name: Thr->Trp
-def: "Thr->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1211]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1211"
-xref: delta_mono_mass "85.031634"
-xref: delta_avge_mass "85.106"
-xref: delta_composition "H(3) C(7) N O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:04:08"
-xref: date_time_modified "2011-06-23 11:04:08"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1212
-name: Thr->Tyr
-def: "Thr->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1212]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1212"
-xref: delta_mono_mass "62.01565"
-xref: delta_avge_mass "62.0694"
-xref: delta_composition "H(2) C(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:04:28"
-xref: date_time_modified "2011-06-23 11:04:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1213
-name: Val->Cys
-def: "Val->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1213]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1213"
-xref: delta_mono_mass "3.940771"
-xref: delta_avge_mass "4.0118"
-xref: delta_composition "H(-4) C(-2) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:19:57"
-xref: date_time_modified "2011-06-23 11:19:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1214
-name: Val->His
-def: "Val->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1214]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1214"
-xref: delta_mono_mass "37.990498"
-xref: delta_avge_mass "38.0082"
-xref: delta_composition "H(-2) C N(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:20:23"
-xref: date_time_modified "2011-06-23 11:20:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1215
-name: Val->Lys
-def: "Val->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1215]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1215"
-xref: delta_mono_mass "29.026549"
-xref: delta_avge_mass "29.0412"
-xref: delta_composition "H(3) C N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:20:45"
-xref: date_time_modified "2011-06-23 11:20:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1216
-name: Val->Asn
-def: "Val->Asn substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1216]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1216"
-xref: delta_mono_mass "14.974514"
-xref: delta_avge_mass "14.9716"
-xref: delta_composition "H(-3) C(-1) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:21:04"
-xref: date_time_modified "2011-06-23 11:21:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1217
-name: Val->Pro
-def: "Val->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1217]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1217"
-xref: delta_mono_mass "-2.01565"
-xref: delta_avge_mass "-2.0159"
-xref: delta_composition "H(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:21:23"
-xref: date_time_modified "2011-06-23 11:21:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1218
-name: Val->Gln
-def: "Val->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1218]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1218"
-xref: delta_mono_mass "28.990164"
-xref: delta_avge_mass "28.9982"
-xref: delta_composition "H(-1) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:21:42"
-xref: date_time_modified "2011-06-23 11:21:42"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1219
-name: Val->Arg
-def: "Val->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1219]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1219"
-xref: delta_mono_mass "57.032697"
-xref: delta_avge_mass "57.0546"
-xref: delta_composition "H(3) C N(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:22:05"
-xref: date_time_modified "2011-06-23 11:22:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1220
-name: Val->Ser
-def: "Val->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1220]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1220"
-xref: delta_mono_mass "-12.036386"
-xref: delta_avge_mass "-12.0538"
-xref: delta_composition "H(-4) C(-2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:22:26"
-xref: date_time_modified "2011-06-23 11:22:26"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1221
-name: Val->Thr
-def: "Val->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1221]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1221"
-xref: delta_mono_mass "1.979265"
-xref: delta_avge_mass "1.9728"
-xref: delta_composition "H(-2) C(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:22:49"
-xref: date_time_modified "2011-06-23 11:22:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1222
-name: Val->Trp
-def: "Val->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1222]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1222"
-xref: delta_mono_mass "87.010899"
-xref: delta_avge_mass "87.0788"
-xref: delta_composition "H C(6) N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:23:11"
-xref: date_time_modified "2011-06-23 11:23:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1223
-name: Val->Tyr
-def: "Val->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1223]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1223"
-xref: delta_mono_mass "63.994915"
-xref: delta_avge_mass "64.0422"
-xref: delta_composition "C(4) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:23:33"
-xref: date_time_modified "2011-06-23 11:23:33"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1224
-name: Trp->Ala
-def: "Trp->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1224]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1224"
-xref: delta_mono_mass "-115.042199"
-xref: delta_avge_mass "-115.132"
-xref: delta_composition "H(-5) C(-8) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:39:07"
-xref: date_time_modified "2011-06-23 11:39:07"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1225
-name: Trp->Asp
-def: "Trp->Asp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1225]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1225"
-xref: delta_mono_mass "-71.05237"
-xref: delta_avge_mass "-71.1225"
-xref: delta_composition "H(-5) C(-7) N(-1) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:40:26"
-xref: date_time_modified "2011-06-23 11:40:26"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1226
-name: Trp->Glu
-def: "Trp->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1226]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1226"
-xref: delta_mono_mass "-57.03672"
-xref: delta_avge_mass "-57.0959"
-xref: delta_composition "H(-3) C(-6) N(-1) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:40:48"
-xref: date_time_modified "2011-06-23 11:40:48"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1227
-name: Trp->Phe
-def: "Trp->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1227]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1227"
-xref: delta_mono_mass "-39.010899"
-xref: delta_avge_mass "-39.036"
-xref: delta_composition "H(-1) C(-2) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:41:09"
-xref: date_time_modified "2011-06-23 11:41:09"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1228
-name: Trp->His
-def: "Trp->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1228]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1228"
-xref: delta_mono_mass "-49.020401"
-xref: delta_avge_mass "-49.0706"
-xref: delta_composition "H(-3) C(-5) N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:41:32"
-xref: date_time_modified "2011-06-23 11:41:32"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1229
-name: Trp->Lys
-def: "Trp->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1229]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1229"
-xref: delta_mono_mass "-57.98435"
-xref: delta_avge_mass "-58.0376"
-xref: delta_composition "H(2) C(-5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:41:52"
-xref: date_time_modified "2011-06-23 11:41:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1230
-name: Trp->Met
-def: "Trp->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1230]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1230"
-xref: delta_mono_mass "-55.038828"
-xref: delta_avge_mass "-55.0138"
-xref: delta_composition "H(-1) C(-6) N(-1) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:42:11"
-xref: date_time_modified "2011-06-23 11:42:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1231
-name: Trp->Asn
-def: "Trp->Asn substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1231]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1231"
-xref: delta_mono_mass "-72.036386"
-xref: delta_avge_mass "-72.1073"
-xref: delta_composition "H(-4) C(-7) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:42:32"
-xref: date_time_modified "2011-06-23 11:42:32"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1232
-name: Trp->Pro
-def: "Trp->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1232]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1232"
-xref: delta_mono_mass "-89.026549"
-xref: delta_avge_mass "-89.0947"
-xref: delta_composition "H(-3) C(-6) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:42:53"
-xref: date_time_modified "2011-06-23 11:42:53"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1233
-name: Trp->Gln
-def: "Trp->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1233]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1233"
-xref: delta_mono_mass "-58.020735"
-xref: delta_avge_mass "-58.0807"
-xref: delta_composition "H(-2) C(-6) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:43:14"
-xref: date_time_modified "2011-06-23 11:43:14"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1234
-name: Trp->Thr
-def: "Trp->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1234]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1234"
-xref: delta_mono_mass "-85.031634"
-xref: delta_avge_mass "-85.106"
-xref: delta_composition "H(-3) C(-7) N(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:43:34"
-xref: date_time_modified "2011-06-23 11:43:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1235
-name: Trp->Val
-def: "Trp->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1235]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1235"
-xref: delta_mono_mass "-87.010899"
-xref: delta_avge_mass "-87.0788"
-xref: delta_composition "H(-1) C(-6) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:43:54"
-xref: date_time_modified "2011-06-23 11:43:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1236
-name: Trp->Tyr
-def: "Trp->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1236]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1236"
-xref: delta_mono_mass "-23.015984"
-xref: delta_avge_mass "-23.0366"
-xref: delta_composition "H(-1) C(-2) N(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:44:18"
-xref: date_time_modified "2011-06-23 11:44:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1237
-name: Tyr->Ala
-def: "Tyr->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1237]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1237"
-xref: delta_mono_mass "-92.026215"
-xref: delta_avge_mass "-92.0954"
-xref: delta_composition "H(-4) C(-6) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:46:23"
-xref: date_time_modified "2011-06-23 11:46:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1238
-name: Tyr->Glu
-def: "Tyr->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1238]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1238"
-xref: delta_mono_mass "-34.020735"
-xref: delta_avge_mass "-34.0593"
-xref: delta_composition "H(-2) C(-4) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:46:45"
-xref: date_time_modified "2011-06-23 11:46:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1239
-name: Tyr->Gly
-def: "Tyr->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1239]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1239"
-xref: delta_mono_mass "-106.041865"
-xref: delta_avge_mass "-106.1219"
-xref: delta_composition "H(-6) C(-7) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:47:05"
-xref: date_time_modified "2011-06-23 11:47:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1240
-name: Tyr->Lys
-def: "Tyr->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1240]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1240"
-xref: delta_mono_mass "-34.968366"
-xref: delta_avge_mass "-35.001"
-xref: delta_composition "H(3) C(-3) N O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:47:23"
-xref: date_time_modified "2011-06-23 11:47:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1241
-name: Tyr->Met
-def: "Tyr->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1241]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1241"
-xref: delta_mono_mass "-32.022844"
-xref: delta_avge_mass "-31.9772"
-xref: delta_composition "C(-4) O(-1) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:47:43"
-xref: date_time_modified "2011-06-23 11:47:43"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1242
-name: Tyr->Pro
-def: "Tyr->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1242]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1242"
-xref: delta_mono_mass "-66.010565"
-xref: delta_avge_mass "-66.0581"
-xref: delta_composition "H(-2) C(-4) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:48:07"
-xref: date_time_modified "2011-06-23 11:48:07"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1243
-name: Tyr->Gln
-def: "Tyr->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1243]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1243"
-xref: delta_mono_mass "-35.004751"
-xref: delta_avge_mass "-35.044"
-xref: delta_composition "H(-1) C(-4) N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:48:28"
-xref: date_time_modified "2011-06-23 11:48:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1244
-name: Tyr->Arg
-def: "Tyr->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1244]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1244"
-xref: delta_mono_mass "-6.962218"
-xref: delta_avge_mass "-6.9876"
-xref: delta_composition "H(3) C(-3) N(3) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:48:49"
-xref: date_time_modified "2011-06-23 11:48:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1245
-name: Tyr->Thr
-def: "Tyr->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1245]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1245"
-xref: delta_mono_mass "-62.01565"
-xref: delta_avge_mass "-62.0694"
-xref: delta_composition "H(-2) C(-5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:49:10"
-xref: date_time_modified "2011-06-23 11:49:10"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1246
-name: Tyr->Val
-def: "Tyr->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1246]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1246"
-xref: delta_mono_mass "-63.994915"
-xref: delta_avge_mass "-64.0422"
-xref: delta_composition "C(-4) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:49:30"
-xref: date_time_modified "2011-06-23 11:49:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1247
-name: Tyr->Trp
-def: "Tyr->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1247]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1247"
-xref: delta_mono_mass "23.015984"
-xref: delta_avge_mass "23.0366"
-xref: delta_composition "H C(2) N O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:49:50"
-xref: date_time_modified "2011-06-23 11:49:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1248
-name: Tyr->Xle
-def: "Tyr->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1248]
-xref: record_id "1248"
-xref: delta_mono_mass "-49.979265"
-xref: delta_avge_mass "-50.0156"
-xref: delta_composition "H(2) C(-3) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:53:26"
-xref: date_time_modified "2011-06-23 11:53:26"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1249
-name: AHA-SS
-def: "Azidohomoalanine coupled to reductively cleaved tag." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1249]
-xref: record_id "1249"
-xref: delta_mono_mass "195.075625"
-xref: delta_avge_mass "195.1787"
-xref: delta_composition "H(9) C(7) N(5) O(2)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-24 10:58:26"
-xref: date_time_modified "2011-06-27 17:38:32"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Multiple"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1250
-name: AHA-SS_CAM
-def: "Carbamidomethylated form of reductively cleaved tag coupled to azidohomoalanine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1250]
-xref: record_id "1250"
-xref: delta_mono_mass "252.097088"
-xref: delta_avge_mass "252.23"
-xref: delta_composition "H(12) C(9) N(6) O(3)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-24 11:00:11"
-xref: date_time_modified "2011-06-27 17:39:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Multiple"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1251
-name: Biotin:Thermo-33033
-def: "Sulfo-SBED Label Photoreactive Biotin Crosslinker." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1251]
-xref: record_id "1251"
-xref: delta_mono_mass "548.223945"
-xref: delta_avge_mass "548.7211"
-xref: delta_composition "H(36) C(25) N(6) O(4) S(2)"
-xref: username_of_poster "Magnojunqueira"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-24 16:58:05"
-xref: date_time_modified "2013-04-16 23:21:26"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "Sulfo-SBED Label Transfer ReagentrnReaction path that does not remove one Hidrogen atom from the target peptide"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1252
-name: Biotin:Thermo-33033-H
-def: "Sulfo-SBED Label Photoreactive Biotin Crosslinker minus Hydrogen." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1252]
-xref: record_id "1252"
-xref: delta_mono_mass "546.208295"
-xref: delta_avge_mass "546.7053"
-xref: delta_composition "H(34) C(25) N(6) O(4) S(2)"
-xref: username_of_poster "Magnojunqueira"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-24 17:01:13"
-xref: date_time_modified "2011-06-24 21:16:06"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "Sulfo-SBED Label Transfer Reagent. Reaction path that removes one Hydrogen atom from the target peptide"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1253
-name: 2-monomethylsuccinyl
-def: "S-(2-monomethylsuccinyl) cysteine." [URL:http\://www.chemblink.com/products/2756-87-8.htm, PMID:http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=5369209, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1253]
-xref: record_id "1253"
-xref: delta_mono_mass "130.026609"
-xref: delta_avge_mass "130.0987"
-xref: delta_composition "H(6) C(5) O(4)"
-xref: username_of_poster "JMcGouran"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-28 15:27:43"
-xref: date_time_modified "2011-07-12 14:25:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1254
-name: Saligenin
-def: "O-toluene." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1254]
-comment: Believed to be created in a secondary reaction after initial formation of an adduct between the organophosphate 2-(o-cresyl)-4H-1,3,2-benzodioxaphosphorane-2-one and Tyr or Ser in proteins.
-xref: record_id "1254"
-xref: delta_mono_mass "106.041865"
-xref: delta_avge_mass "106.1219"
-xref: delta_composition "H(6) C(7) O"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-30 19:24:11"
-xref: date_time_modified "2011-07-09 09:17:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1255
-name: Cresylphosphate
-def: "O-toluyl-phosphorylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1255]
-comment: Created by hydrolysis of the product of the reaction of 2-(o-cresyl)-4H-1,3,2-benzodioxaphosphorane-2-one with amino acids residues in proteins.
-xref: record_id "1255"
-xref: delta_mono_mass "170.013281"
-xref: delta_avge_mass "170.1024"
-xref: delta_composition "H(7) C(7) O(3) P"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-30 19:33:14"
-xref: date_time_modified "2011-07-09 09:20:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "R"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "S"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "T"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "Y"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1256
-name: CresylSaligeninPhosphate
-def: "Cresyl-Saligenin-phosphorylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1256]
-comment: Created by reaction of 2-(o-cresyl)-4H-1,3,2-benzodioxaphosphorane-2-one with amino acid residues in proteins.
-xref: record_id "1256"
-xref: delta_mono_mass "276.055146"
-xref: delta_avge_mass "276.2244"
-xref: delta_composition "H(13) C(14) O(4) P"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-30 19:38:15"
-xref: date_time_modified "2011-07-09 09:21:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "R"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "S"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "T"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "Y"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1257
-name: Ub-Br2
-def: "Ub Bromide probe addition." [URL:http\://www.enzolifesciences.com/fileadmin/reports/els_0a605e18ec.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1257]
-synonym: "Active site DUB cystine modification with Br Ub probe Trypsin Digestion reminant of Ub Br probe" RELATED []
-xref: record_id "1257"
-xref: delta_mono_mass "100.063663"
-xref: delta_avge_mass "100.1191"
-xref: delta_composition "H(8) C(4) N(2) O"
-xref: username_of_poster "JMcGouran"
-xref: group_of_poster ""
-xref: date_time_posted "2011-07-01 13:25:05"
-xref: date_time_modified "2011-07-11 11:30:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1258
-name: Ub-VME
-def: "Ubiquitin vinylmethylester." [URL:http\://www.lifesensors.com/pdf/Ub-VME_datasheet.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1258]
-synonym: "Active site DUB cystine modification with VME Ub probe Trypsin Digestion reminant of Ub VMEr probe" RELATED []
-xref: record_id "1258"
-xref: delta_mono_mass "172.084792"
-xref: delta_avge_mass "172.1818"
-xref: delta_composition "H(12) C(7) N(2) O(3)"
-xref: username_of_poster "JMcGouran"
-xref: group_of_poster ""
-xref: date_time_posted "2011-07-01 13:27:56"
-xref: date_time_modified "2021-07-06 12:32:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1261
-name: Ub-fluorescein
-def: "Ub Fluorescein probe addition." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1261]
-comment: Unpublished chemically synthesized protein modification tool.
-synonym: "Active site DUB cystine modification with Fluorescein Ub probe Trypsin Digestion reminant of Ub Fluorescein probe" RELATED []
-xref: record_id "1261"
-xref: delta_mono_mass "597.209772"
-xref: delta_avge_mass "597.598"
-xref: delta_composition "H(29) C(31) N(6) O(7)"
-xref: username_of_poster "JMcGouran"
-xref: group_of_poster ""
-xref: date_time_posted "2011-07-01 13:49:56"
-xref: date_time_modified "2011-07-12 14:28:20"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1262
-name: 2-dimethylsuccinyl
-def: "S-(2-dimethylsuccinyl) cysteine." [PMID:http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=637568&loc=ec_rcs, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1262]
-xref: record_id "1262"
-xref: delta_mono_mass "144.042259"
-xref: delta_avge_mass "144.1253"
-xref: delta_composition "H(8) C(6) O(4)"
-xref: username_of_poster "JMcGouran"
-xref: group_of_poster ""
-xref: date_time_posted "2011-07-06 10:55:02"
-xref: date_time_modified "2011-07-12 14:25:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1263
-name: Gly
-def: "Addition of Glycine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1263]
-comment: Occasionally used as chemical tag. In most cases, +57 is actually over-alkylation with iodoacetamide.
-xref: record_id "1263"
-xref: delta_mono_mass "57.021464"
-xref: delta_avge_mass "57.0513"
-xref: delta_composition "H(3) C(2) N O"
-xref: username_of_poster "kstampe2"
-xref: group_of_poster ""
-xref: date_time_posted "2011-07-07 16:37:10"
-xref: date_time_modified "2020-10-05 09:16:08"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1264
-name: pupylation
-def: "Addition of GGE." [PMID:21738222, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1264]
-xref: record_id "1264"
-xref: delta_mono_mass "243.085521"
-xref: delta_avge_mass "243.2166"
-xref: delta_composition "H(13) C(9) N(3) O(5)"
-xref: username_of_poster "hbromage"
-xref: group_of_poster ""
-xref: date_time_posted "2011-07-13 21:34:29"
-xref: date_time_modified "2011-07-24 12:24:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1266
-name: Label:13C(4)
-def: "13C4 Methionine label." [URL:http\://www.pil.sdu.dk/silac_intro.htm, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1266]
-synonym: "SILAC" RELATED []
-xref: record_id "1266"
-xref: delta_mono_mass "4.013419"
-xref: delta_avge_mass "3.9706"
-xref: delta_composition "C(-4) 13C(4)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2011-07-27 09:55:40"
-xref: date_time_modified "2011-12-07 10:49:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1267
-name: Label:13C(4)+Oxidation
-def: "Oxidised 13C4 labelled Methionine." [URL:http\://www.pil.sdu.dk/silac_intro.htm, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1267]
-synonym: "SILAC" RELATED []
-xref: record_id "1267"
-xref: delta_mono_mass "20.008334"
-xref: delta_avge_mass "19.97"
-xref: delta_composition "C(-4) 13C(4) O"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2011-07-27 10:10:30"
-xref: date_time_modified "2011-08-05 14:17:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1270
-name: HCysThiolactone
-def: "N-Homocysteine thiolactone." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1270]
-xref: record_id "1270"
-xref: delta_mono_mass "117.024835"
-xref: delta_avge_mass "117.1695"
-xref: delta_composition "H(7) C(4) N O S"
-xref: username_of_poster "alejandro"
-xref: group_of_poster ""
-xref: date_time_posted "2011-09-15 19:31:10"
-xref: date_time_modified "2014-12-01 10:35:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_1_misc_notes "N-Homocysteine thiolactone is an acylating agent and can react with the E amino group of lysine residues"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1271
-name: HCysteinyl
-def: "S-homocysteinylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1271]
-xref: record_id "1271"
-xref: delta_mono_mass "133.019749"
-xref: delta_avge_mass "133.1689"
-xref: delta_composition "H(7) C(4) N O(2) S"
-xref: username_of_poster "alejandro"
-xref: group_of_poster ""
-xref: date_time_posted "2011-09-15 19:36:44"
-xref: date_time_modified "2024-08-12 10:20:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_1_misc_notes "Homocysteine can take part in disulfide exchange reactions with S-S bonds in proteins, thus forming S-homocysteinylated proteins"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1276
-name: UgiJoullie
-def: "Side reaction of HisTag." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1276]
-comment: Side product of the three component Ugi-Joullie reaction. Pirrolidine is reacted with a isocianide modificated peptide (CNGGHHHHHH) to get a Pro-Gly-GGHHHHHH. The main product is the C-terminal modified protein. Unlikely Asp and Glu can react.
-xref: record_id "1276"
-xref: delta_mono_mass "1106.48935"
-xref: delta_avge_mass "1107.1274"
-xref: delta_composition "H(60) C(47) N(23) O(10)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2011-09-26 12:42:53"
-xref: date_time_modified "2011-09-30 12:38:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "E"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1277
-name: Dipyridyl
-def: "Cys modified with dipy ligand." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1277]
-comment: Cysteine residue reacts with a chlorinated dipyridyl ligand to get a monoalkylated Cys-L1. The only product is this single cys mutant modified on that position.
-xref: record_id "1277"
-xref: delta_mono_mass "225.090212"
-xref: delta_avge_mass "225.2459"
-xref: delta_composition "H(11) C(13) N(3) O"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2011-09-27 18:33:34"
-xref: date_time_modified "2012-01-20 14:46:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1278
-name: Furan
-def: "Chemical modification of the iodinated sites of thyroglobulin by Suzuki reaction." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1278]
-xref: record_id "1278"
-xref: delta_mono_mass "66.010565"
-xref: delta_avge_mass "66.0581"
-xref: delta_composition "H(2) C(4) O"
-xref: username_of_poster "chem0303"
-xref: group_of_poster ""
-xref: date_time_posted "2011-09-28 13:31:35"
-xref: date_time_modified "2011-09-30 12:39:48"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1279
-name: Difuran
-def: "Chemical modification of the diiodinated sites of thyroglobulin by Suzuki reaction." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1279]
-xref: record_id "1279"
-xref: delta_mono_mass "132.021129"
-xref: delta_avge_mass "132.1162"
-xref: delta_composition "H(4) C(8) O(2)"
-xref: username_of_poster "chem0303"
-xref: group_of_poster ""
-xref: date_time_posted "2011-09-28 13:34:45"
-xref: date_time_modified "2011-09-30 12:40:21"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1281
-name: BMP-piperidinol
-def: "1-methyl-3-benzoyl-4-hydroxy-4-phenylpiperidine." [PMID:http://www.ncbi.nlm.nih.gov/pubmed/11869872, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1281]
-synonym: "(4-hydroxy-1-methyl-4-phenylpiperidin-3-yl)(phenyl)methanone 3-benzoyl-1-methyl-4-phenyl-4-piperidinol" RELATED []
-xref: record_id "1281"
-xref: delta_mono_mass "263.131014"
-xref: delta_avge_mass "263.3337"
-xref: delta_composition "H(17) C(18) N O"
-xref: username_of_poster "Areej"
-xref: group_of_poster ""
-xref: date_time_posted "2011-10-12 12:22:26"
-xref: date_time_modified "2012-01-13 15:44:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1282
-name: UgiJoullieProGly
-def: "Side reaction of PG with Side chain of aspartic or glutamic acid." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1282]
-comment: Side product of the three component Ugi-Joullie reaction. Pirrolidine is reacted with a isocianide modificated glycine to get Protein-Pro-Gly. The main product is the C-terminal modified protein. Unlikely Asp and Glu can react.
-xref: record_id "1282"
-xref: delta_mono_mass "154.074228"
-xref: delta_avge_mass "154.1665"
-xref: delta_composition "H(10) C(7) N(2) O(2)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2011-10-14 18:11:28"
-xref: date_time_modified "2011-10-21 16:41:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "E"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1283
-name: UgiJoullieProGlyProGly
-def: "Side reaction of PGPG with Side chain of aspartic or glutamic acid." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1283]
-comment: Side product of the three component Ugi-Joullie reaction. Pirrolidine is reacted with a isocianide modificated glycine to get Protein-Pro-Gly-Pro-Gly. The main product is the C-terminal modified protein. Unlikely Asp and Glu can react.
-xref: record_id "1283"
-xref: delta_mono_mass "308.148455"
-xref: delta_avge_mass "308.333"
-xref: delta_composition "H(20) C(14) N(4) O(4)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2011-10-14 18:14:19"
-xref: date_time_modified "2011-10-21 16:40:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "E"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1286
-name: IMEHex(2)NeuAc(1)
-def: "Glycosylation with IME linked Hex(2) NeuAc." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1286]
-comment: Modification by Hex(2) NeuAc using IME coupling to get glycosylated proteins.
-synonym: "(2-Imino-2-methoxyethyl 1-thioglycoside)" RELATED []
-xref: record_id "1286"
-xref: delta_mono_mass "688.199683"
-xref: delta_avge_mass "688.6527"
-xref: delta_composition "H(3) C(2) N S Hex(2) NeuAc"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-11 12:06:36"
-xref: date_time_modified "2015-05-01 14:20:42"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other glycosylation"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1287
-name: Arg-loss
-def: "Loss of arginine due to transpeptidation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1287]
-xref: record_id "1287"
-xref: delta_mono_mass "-156.101111"
-xref: delta_avge_mass "-156.1857"
-xref: delta_composition "H(-12) C(-6) N(-4) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-21 10:12:18"
-xref: date_time_modified "2011-11-24 16:39:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Any C-term"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1288
-name: Arg
-def: "Addition of arginine due to transpeptidation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1288]
-xref: record_id "1288"
-xref: delta_mono_mass "156.101111"
-xref: delta_avge_mass "156.1857"
-xref: delta_composition "H(12) C(6) N(4) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-21 10:15:00"
-xref: date_time_modified "2011-11-21 10:17:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1289
-name: Butyryl
-def: "Butyryl." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1289]
-xref: record_id "1289"
-xref: delta_mono_mass "70.041865"
-xref: delta_avge_mass "70.0898"
-xref: delta_composition "H(6) C(4) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-21 12:06:20"
-xref: date_time_modified "2024-08-12 10:01:08"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1290
-name: Dicarbamidomethyl
-def: "Double Carbamidomethylation." [PMID:18511913, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1290]
-comment: Mentioned by Marshall Bern.
-xref: record_id "1290"
-xref: delta_mono_mass "114.042927"
-xref: delta_avge_mass "114.1026"
-xref: delta_composition "H(6) C(4) N(2) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-21 13:21:06"
-xref: date_time_modified "2013-05-16 10:59:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Artefact"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "R"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Artefact"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "N-term"
-xref: spec_5_position "Any N-term"
-xref: spec_5_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1291
-name: Dimethyl:2H(6)
-def: "Dimethyl-Medium." [PMID:15782174, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1291]
-xref: record_id "1291"
-xref: delta_mono_mass "34.068961"
-xref: delta_avge_mass "34.0901"
-xref: delta_composition "H(-2) 2H(6) C(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-21 13:27:00"
-xref: date_time_modified "2013-02-22 12:32:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "R"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1292
-name: GGQ
-def: "SUMOylation leaving GlyGlyGln." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1292]
-xref: record_id "1292"
-xref: delta_mono_mass "242.101505"
-xref: delta_avge_mass "242.2319"
-xref: delta_composition "H(14) C(9) N(4) O(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-21 13:37:45"
-xref: date_time_modified "2011-11-21 13:53:21"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_1_misc_notes "This peptide is generated from a trypsin/chymotrypsin dual digest."
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1293
-name: QTGG
-def: "SUMOylation leaving GlnThrGlyGly." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1293]
-xref: record_id "1293"
-xref: delta_mono_mass "343.149184"
-xref: delta_avge_mass "343.3357"
-xref: delta_composition "H(21) C(13) N(5) O(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-21 13:41:32"
-xref: date_time_modified "2011-11-25 13:05:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_1_misc_notes "This peptide is generated from a trypsin/chymotrypsin dual digest."
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1296
-name: Label:13C(3)
-def: "13C3 label for SILAC." [URL:http\://www.pil.sdu.dk/silac_intro.htm, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1296]
-xref: record_id "1296"
-xref: delta_mono_mass "3.010064"
-xref: delta_avge_mass "2.978"
-xref: delta_composition "C(-3) 13C(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-21 14:36:18"
-xref: date_time_modified "2011-11-21 14:37:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1297
-name: Label:13C(3)15N(1)
-def: "SILAC or AQUA label." [URL:http\://www.pil.sdu.dk/silac_intro.htm, URL:https\://www.thermofisher.com/order/catalog/product/A40010#/A40010, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1297]
-xref: record_id "1297"
-xref: delta_mono_mass "4.007099"
-xref: delta_avge_mass "3.9714"
-xref: delta_composition "C(-3) 13C(3) N(-1) 15N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-21 14:37:53"
-xref: date_time_modified "2020-01-09 09:44:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1298
-name: Label:13C(4)15N(1)
-def: "13C4 15N1 label for SILAC." [URL:http\://www.pil.sdu.dk/silac_intro.htm, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1298]
-xref: record_id "1298"
-xref: delta_mono_mass "5.010454"
-xref: delta_avge_mass "4.964"
-xref: delta_composition "C(-4) 13C(4) N(-1) 15N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-21 14:40:56"
-xref: date_time_modified "2011-11-21 14:40:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1299
-name: Label:2H(10)
-def: "2H(10) label." [URL:http\://www.pil.sdu.dk/silac_intro.htm, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1299]
-xref: record_id "1299"
-xref: delta_mono_mass "10.062767"
-xref: delta_avge_mass "10.0616"
-xref: delta_composition "H(-10) 2H(10)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-21 14:51:01"
-xref: date_time_modified "2011-11-21 14:51:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1300
-name: Label:2H(4)13C(1)
-def: "Label:2H(4)13C(1)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1300]
-comment: For SILAC experiments.
-xref: record_id "1300"
-xref: delta_mono_mass "5.028462"
-xref: delta_avge_mass "5.0173"
-xref: delta_composition "H(-4) 2H(4) C(-1) 13C"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-21 14:52:54"
-xref: date_time_modified "2011-11-21 14:52:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1301
-name: Lys
-def: "Addition of lysine due to transpeptidation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1301]
-xref: record_id "1301"
-xref: delta_mono_mass "128.094963"
-xref: delta_avge_mass "128.1723"
-xref: delta_composition "H(12) C(6) N(2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-21 14:56:07"
-xref: date_time_modified "2015-05-06 12:07:14"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1302
-name: mTRAQ:13C(6)15N(2)
-def: "MTRAQ heavy." [URL:http\://www3.appliedbiosystems.com/cms/groups/psm_support/documents/generaldocuments/cms_054141.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1302]
-synonym: "Applied Biosystems mTRAQ(TM) reagent" RELATED []
-xref: record_id "1302"
-xref: delta_mono_mass "148.109162"
-xref: delta_avge_mass "148.1257"
-xref: delta_composition "H(12) C 13C(6) 15N(2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-25 10:35:32"
-xref: date_time_modified "2011-11-25 10:35:32"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "0"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Low abundance"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "H"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "Very low abundance"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "S"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Isotopic label"
-xref: spec_5_misc_notes "Very low abundance"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "T"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Isotopic label"
-xref: spec_6_misc_notes "Very low abundance"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1303
-name: NeuAc
-def: "N-acetyl neuraminic acid." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1303]
-xref: record_id "1303"
-xref: delta_mono_mass "291.095417"
-xref: delta_avge_mass "291.2546"
-xref: delta_composition "NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-25 10:40:54"
-xref: date_time_modified "2015-05-01 15:11:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_292_mono_mass "291.095417"
-xref: spec_1_neutral_loss_292_avge_mass "291.2546"
-xref: spec_1_neutral_loss_292_flag "false"
-xref: spec_1_neutral_loss_292_composition "NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_292_mono_mass "291.095417"
-xref: spec_2_neutral_loss_292_avge_mass "291.2546"
-xref: spec_2_neutral_loss_292_flag "false"
-xref: spec_2_neutral_loss_292_composition "NeuAc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_292_mono_mass "291.095417"
-xref: spec_2_neutral_loss_292_avge_mass "291.2546"
-xref: spec_2_neutral_loss_292_flag "false"
-xref: spec_2_neutral_loss_292_composition "NeuAc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1304
-name: NeuGc
-def: "N-glycoyl neuraminic acid." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1304]
-xref: record_id "1304"
-xref: delta_mono_mass "307.090331"
-xref: delta_avge_mass "307.254"
-xref: delta_composition "NeuGc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-25 10:41:35"
-xref: date_time_modified "2015-05-01 15:13:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_308_mono_mass "307.090331"
-xref: spec_1_neutral_loss_308_avge_mass "307.254"
-xref: spec_1_neutral_loss_308_flag "false"
-xref: spec_1_neutral_loss_308_composition "NeuGc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_308_mono_mass "307.090331"
-xref: spec_2_neutral_loss_308_avge_mass "307.254"
-xref: spec_2_neutral_loss_308_flag "false"
-xref: spec_2_neutral_loss_308_composition "NeuGc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_308_mono_mass "307.090331"
-xref: spec_2_neutral_loss_308_avge_mass "307.254"
-xref: spec_2_neutral_loss_308_flag "false"
-xref: spec_2_neutral_loss_308_composition "NeuGc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1305
-name: Propyl
-def: "Propyl." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1305]
-xref: record_id "1305"
-xref: delta_mono_mass "42.04695"
-xref: delta_avge_mass "42.0797"
-xref: delta_composition "H(6) C(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-25 11:06:09"
-xref: date_time_modified "2014-10-17 11:31:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "D"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_misc_notes "propyl ester"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "E"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_4_misc_notes "propyl ester"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "C-term"
-xref: spec_5_position "Any C-term"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_5_misc_notes "propyl ester"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "C-term"
-xref: spec_6_position "Protein C-term"
-xref: spec_6_classification "Chemical derivative"
-xref: spec_6_misc_notes "propyl ester"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1306
-name: Propyl:2H(6)
-def: "Propyl:2H(6)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1306]
-xref: record_id "1306"
-xref: delta_mono_mass "48.084611"
-xref: delta_avge_mass "48.1167"
-xref: delta_composition "2H(6) C(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-25 11:06:56"
-xref: date_time_modified "2011-11-25 11:06:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1310
-name: Propiophenone
-def: "Propiophenone." [PMID:http://www.ncbi.nlm.nih.gov/pubmed/11869872, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1310]
-xref: record_id "1310"
-xref: delta_mono_mass "132.057515"
-xref: delta_avge_mass "132.1592"
-xref: delta_composition "H(8) C(9) O"
-xref: username_of_poster "Areej"
-xref: group_of_poster ""
-xref: date_time_posted "2011-12-07 23:43:34"
-xref: date_time_modified "2011-12-09 13:50:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "R"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "S"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "T"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "W"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "C"
-xref: spec_7_position "Anywhere"
-xref: spec_7_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1312
-name: Delta:H(6)C(3)O(1)
-def: "Reduced acrolein addition +58." [PMID:21778411, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1312]
-xref: record_id "1312"
-xref: delta_mono_mass "58.041865"
-xref: delta_avge_mass "58.0791"
-xref: delta_composition "H(6) C(3) O"
-xref: username_of_poster "yiyingzhu"
-xref: group_of_poster ""
-xref: date_time_posted "2011-12-15 19:38:31"
-xref: date_time_modified "2011-12-16 15:11:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "N-term"
-xref: spec_4_position "Protein N-term"
-xref: spec_4_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1313
-name: Delta:H(8)C(6)O(1)
-def: "Reduced acrolein addition +96." [PMID:21778411, PMID:9632657, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1313]
-xref: record_id "1313"
-xref: delta_mono_mass "96.057515"
-xref: delta_avge_mass "96.1271"
-xref: delta_composition "H(8) C(6) O"
-xref: username_of_poster "yiyingzhu"
-xref: group_of_poster ""
-xref: date_time_posted "2011-12-15 19:48:15"
-xref: date_time_modified "2015-10-12 16:16:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1314
-name: biotinAcrolein298
-def: "Biotin hydrazide labeled acrolein addition +298." [PMID:21704744, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1314]
-xref: record_id "1314"
-xref: delta_mono_mass "298.146347"
-xref: delta_avge_mass "298.4044"
-xref: delta_composition "H(22) C(13) N(4) O(2) S"
-xref: username_of_poster "yiyingzhu"
-xref: group_of_poster ""
-xref: date_time_posted "2011-12-15 19:54:52"
-xref: date_time_modified "2011-12-16 15:19:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "N-term"
-xref: spec_4_position "Protein N-term"
-xref: spec_4_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1315
-name: MM-diphenylpentanone
-def: "3-methyl-5-(methylamino)-1,3-diphenylpentan-1-one." [PMID:http://www.ncbi.nlm.nih.gov/pubmed/11869872, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1315]
-xref: record_id "1315"
-xref: delta_mono_mass "265.146664"
-xref: delta_avge_mass "265.3496"
-xref: delta_composition "H(19) C(18) N O"
-xref: username_of_poster "Areej"
-xref: group_of_poster ""
-xref: date_time_posted "2011-12-21 21:29:00"
-xref: date_time_modified "2011-12-21 21:29:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1317
-name: EHD-diphenylpentanone
-def: "2-ethyl-3-hydroxy-1,3-diphenylpentan-1-one." [PMID:http://www.ncbi.nlm.nih.gov/pubmed/11869872, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1317]
-synonym: "3-benzoyl-1-methyl-4-phenyl-4-piperidinol demethyl damino" RELATED []
-xref: record_id "1317"
-xref: delta_mono_mass "266.13068"
-xref: delta_avge_mass "266.3343"
-xref: delta_composition "H(18) C(18) O(2)"
-xref: username_of_poster "Areej"
-xref: group_of_poster ""
-xref: date_time_posted "2012-01-08 15:22:49"
-xref: date_time_modified "2012-01-13 15:41:26"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "M"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1320
-name: Biotin:Thermo-21901+2H2O
-def: "Maleimide-Biotin + 2Water." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1320]
-synonym: "Maleimide-PEG2-Biotin + 2Water" RELATED []
-xref: record_id "1320"
-xref: delta_mono_mass "561.246849"
-xref: delta_avge_mass "561.6489"
-xref: delta_composition "H(39) C(23) N(5) O(9) S"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2012-01-23 14:20:11"
-xref: date_time_modified "2012-01-27 12:51:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1321
-name: DiLeu4plex115
-def: "Accurate mass for DiLeu 115 isobaric tag." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1321]
-comment: Different channels have the same nominal mass but slightly different exact masses.
-xref: record_id "1321"
-xref: delta_mono_mass "145.12"
-xref: delta_avge_mass "145.1966"
-xref: delta_composition "H(15) C(7) 13C 15N 18O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2012-02-15 12:05:08"
-xref: date_time_modified "2024-08-12 10:00:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Low abundance"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1322
-name: DiLeu4plex
-def: "Accurate mass for DiLeu 116 isobaric tag." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1322]
-comment: Different channels have the same nominal mass but slightly different exact masses.
-synonym: "Representative, nominal mass for all four tags" RELATED []
-xref: record_id "1322"
-xref: delta_mono_mass "145.132163"
-xref: delta_avge_mass "145.2229"
-xref: delta_composition "H(13) 2H(2) C(8) N 18O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2012-02-15 12:05:48"
-xref: date_time_modified "2024-08-12 10:00:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Low abundance"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1323
-name: DiLeu4plex117
-def: "Accurate mass for DiLeu 117 isobaric tag." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1323]
-comment: Different channels have the same nominal mass but slightly different exact masses.
-xref: record_id "1323"
-xref: delta_mono_mass "145.128307"
-xref: delta_avge_mass "145.2092"
-xref: delta_composition "H(13) 2H(2) C(7) 13C 15N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2012-02-15 12:06:10"
-xref: date_time_modified "2024-08-12 10:00:14"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Low abundance"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1324
-name: DiLeu4plex118
-def: "Accurate mass for DiLeu 118 isobaric tag." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1324]
-comment: Different channels have the same nominal mass but slightly different exact masses.
-xref: record_id "1324"
-xref: delta_mono_mass "145.140471"
-xref: delta_avge_mass "145.2354"
-xref: delta_composition "H(11) 2H(4) C(8) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2012-02-15 12:06:30"
-xref: date_time_modified "2024-08-12 09:59:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Low abundance"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1326
-name: NEMsulfur
-def: "N-ethylmaleimideSulfur." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1326]
-synonym: "NEMS" RELATED []
-xref: record_id "1326"
-xref: delta_mono_mass "157.019749"
-xref: delta_avge_mass "157.1903"
-xref: delta_composition "H(7) C(6) N O(2) S"
-xref: username_of_poster "Raghothama"
-xref: group_of_poster ""
-xref: date_time_posted "2012-02-29 17:06:24"
-xref: date_time_modified "2012-03-09 11:26:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1327
-name: SulfurDioxide
-def: "SulfurDioxide." [PMID:http://www.ncbi.nlm.nih.gov/pubmed/21740851, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1327]
-xref: record_id "1327"
-xref: delta_mono_mass "63.9619"
-xref: delta_avge_mass "64.0638"
-xref: delta_composition "O(2) S"
-xref: username_of_poster "Raghothama"
-xref: group_of_poster ""
-xref: date_time_posted "2012-02-29 17:24:24"
-xref: date_time_modified "2012-03-09 11:25:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1328
-name: NEMsulfurWater
-def: "N-ethylmaleimideSulfurWater." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1328]
-synonym: "NEMSwater" RELATED []
-xref: record_id "1328"
-xref: delta_mono_mass "175.030314"
-xref: delta_avge_mass "175.2056"
-xref: delta_composition "H(9) C(6) N O(3) S"
-xref: username_of_poster "Raghothama"
-xref: group_of_poster ""
-xref: date_time_posted "2012-02-29 17:25:30"
-xref: date_time_modified "2012-03-09 11:24:53"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1330
-name: bisANS-sulfonates
-def: "BisANS with loss of both sulfonates." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1330]
-xref: record_id "1330"
-xref: delta_mono_mass "434.178299"
-xref: delta_avge_mass "434.5305"
-xref: delta_composition "H(22) C(32) N(2)"
-xref: username_of_poster "app95d"
-xref: group_of_poster ""
-xref: date_time_posted "2012-05-22 21:55:58"
-xref: date_time_modified "2021-07-06 12:33:24"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1331
-name: DNCB_hapten
-def: "Chemical reaction with 2,4-dinitro-1-chloro benzene (DNCB)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1331]
-comment: Chemical reaction with 2,4-dinitro-1-chloro benzene (DNCB) by nucleophilic attack on electrophilic amino acid side chains.
-xref: record_id "1331"
-xref: delta_mono_mass "166.001457"
-xref: delta_avge_mass "166.0911"
-xref: delta_composition "H(2) C(6) N(2) O(4)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2012-05-24 13:55:30"
-xref: date_time_modified "2012-08-03 09:19:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "Y"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1340
-name: Biotin:Thermo-21911
-def: "Biotin-PEG11-maleimide." [URL:http\://www.piercenet.com/browse.cfm?fldID=E3862D31-9A5C-4F0A-9879-F600D33BD926, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1340]
-synonym: "Thermo #21911" RELATED []
-xref: record_id "1340"
-xref: delta_mono_mass "921.461652"
-xref: delta_avge_mass "922.0913"
-xref: delta_composition "H(71) C(41) N(5) O(16) S"
-xref: username_of_poster "Jolein_Gloerich"
-xref: group_of_poster ""
-xref: date_time_posted "2012-06-26 17:49:31"
-xref: date_time_modified "2012-07-14 19:02:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1341
-name: iodoTMT
-def: "Native iodoacetyl Tandem Mass Tag®." [URL:http\://www.lifetechnologies.com/order/catalog/product/90100, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1341]
-comment: This modification describes the native iodoTMT Reagent without isotopic label. Upon CID, this reagent releases a reporter ion of 126.127725(monoisotopic mass).
-synonym: "Tandem Mass Tag® and TMT® are registered Trademarks of Proteome Sciences plc. iodoTMTzero iodoTMT0" RELATED []
-xref: record_id "1341"
-xref: delta_mono_mass "324.216141"
-xref: delta_avge_mass "324.4185"
-xref: delta_composition "H(28) C(16) N(4) O(3)"
-xref: username_of_poster "rbomgard"
-xref: group_of_poster ""
-xref: date_time_posted "2012-07-06 17:37:43"
-xref: date_time_modified "2024-08-12 10:07:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "D"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "E"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "H"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "K"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1342
-name: iodoTMT6plex
-def: "Sixplex iodoacetyl Tandem Mass Tag®." [URL:http\://www.lifetechnologies.com/order/catalog/product/90102, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1342]
-comment: This modification describes the native iodoTMT Reagent without isotopic label. Upon CID, this reagent releases a reporter ions of 126.127725, 127.124760, 128.134433, 129.131468, 130.141141, and 131.138176 (monoisotopic mass).
-synonym: "Tandem Mass Tag® and TMT® are registered Trademarks of Proteome Sciences plc. iodoTMTsixplex iodoTMT6" RELATED []
-xref: record_id "1342"
-xref: delta_mono_mass "329.226595"
-xref: delta_avge_mass "329.3825"
-xref: delta_composition "H(28) C(12) 13C(4) N(3) 15N O(3)"
-xref: username_of_poster "rbomgard"
-xref: group_of_poster ""
-xref: date_time_posted "2012-07-06 17:43:59"
-xref: date_time_modified "2024-08-12 10:06:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "D"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "E"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "H"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "K"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1344
-name: Phosphogluconoylation
-def: "Phosphogluconoylation." [URL:http\://www.abrf.org/index.cfm/dm.details?DMID=275&AvgMass=258&Margin=0, PMID:18083862, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1344]
-xref: record_id "1344"
-xref: delta_mono_mass "258.014069"
-xref: delta_avge_mass "258.1199"
-xref: delta_composition "H(11) C(6) O(9) P"
-xref: username_of_poster "gwadams"
-xref: group_of_poster ""
-xref: date_time_posted "2012-07-13 14:40:15"
-xref: date_time_modified "2013-05-22 10:55:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1345
-name: PS_Hapten
-def: "Reaction with phenyl salicylate (PS)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1345]
-xref: record_id "1345"
-xref: delta_mono_mass "120.021129"
-xref: delta_avge_mass "120.1055"
-xref: delta_composition "H(4) C(7) O(2)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2012-08-01 14:45:32"
-xref: date_time_modified "2012-08-03 09:20:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1348
-name: Cy3-maleimide
-def: "Cy3 Maleimide mono-Reactive dye." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1348]
-synonym: "Cy3 mono-functional maleimides are used for the selective labeling of molecules containing free sulfhydryl groups, such as cysteine residues in proteins and peptides and oligonucleotides." RELATED []
-xref: record_id "1348"
-xref: delta_mono_mass "753.262796"
-xref: delta_avge_mass "753.9046"
-xref: delta_composition "H(45) C(37) N(4) O(9) S(2)"
-xref: username_of_poster "hbromage"
-xref: group_of_poster ""
-xref: date_time_posted "2012-08-27 21:50:06"
-xref: date_time_modified "2015-01-02 09:46:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1349
-name: benzylguanidine
-def: "Modification of the lysine side chain from NH2 to guanidine with a H removed in favor of a benzyl group." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1349]
-synonym: "adds 132 Da to K side chain" RELATED []
-xref: record_id "1349"
-xref: delta_mono_mass "132.068748"
-xref: delta_avge_mass "132.1625"
-xref: delta_composition "H(8) C(8) N(2)"
-xref: username_of_poster "pepinr"
-xref: group_of_poster ""
-xref: date_time_posted "2012-09-06 17:14:04"
-xref: date_time_modified "2012-09-07 15:15:29"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1350
-name: CarboxymethylDMAP
-def: "A fixed +1 charge tag attached to the N-terminus of peptides." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1350]
-synonym: "Added mass is reduced by 1 H to reflect that first charge state requires no proton addition Replaces one of the N-terminal H atoms with C9H12N2O" RELATED []
-xref: record_id "1350"
-xref: delta_mono_mass "162.079313"
-xref: delta_avge_mass "162.1885"
-xref: delta_composition "H(10) C(9) N(2) O"
-xref: username_of_poster "pepinr"
-xref: group_of_poster ""
-xref: date_time_posted "2012-09-06 17:32:42"
-xref: date_time_modified "2012-09-07 15:19:24"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1355
-name: azole
-def: "Formation of five membered aromatic heterocycle." [PMID:15883371, PMID:8895467, PMID:10200165, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1355]
-xref: record_id "1355"
-xref: delta_mono_mass "-20.026215"
-xref: delta_avge_mass "-20.0312"
-xref: delta_composition "H(-4) O(-1)"
-xref: username_of_poster "jomcintosh"
-xref: group_of_poster ""
-xref: date_time_posted "2012-09-10 17:32:20"
-xref: date_time_modified "2012-09-15 00:33:29"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1356
-name: phosphoRibosyl
-def: "Phosphate-ribosylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1356]
-xref: record_id "1356"
-xref: delta_mono_mass "212.00859"
-xref: delta_avge_mass "212.0945"
-xref: delta_composition "H(9) C(5) O(7) P"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2012-09-19 14:16:08"
-xref: date_time_modified "2024-08-12 09:59:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "E"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "R"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1358
-name: NEM:2H(5)+H2O
-def: "D5 N-ethylmaleimide+water on cysteines." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1358]
-comment: Lab based observation that D5 NEM hydrolyses in an analogous way to NEM.
-synonym: "CysNEM D5 hydrolised" RELATED []
-xref: record_id "1358"
-xref: delta_mono_mass "148.089627"
-xref: delta_avge_mass "148.1714"
-xref: delta_composition "H(4) 2H(5) C(6) N O(3)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2012-10-16 17:45:04"
-xref: date_time_modified "2012-11-02 16:22:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1363
-name: Crotonyl
-def: "Crotonylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1363]
-xref: record_id "1363"
-xref: delta_mono_mass "68.026215"
-xref: delta_avge_mass "68.074"
-xref: delta_composition "H(4) C(4) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2012-12-24 15:50:10"
-xref: date_time_modified "2024-08-12 09:59:07"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1364
-name: O-Et-N-diMePhospho
-def: "O-ethyl, N-dimethyl phosphate." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1364]
-comment: Adduct formed upon reaction of the organophosphate tabun with the active site serine of serine esterases/proteases such as butyrylcholinestease.
-synonym: "tabun" RELATED []
-xref: record_id "1364"
-xref: delta_mono_mass "135.044916"
-xref: delta_avge_mass "135.1015"
-xref: delta_composition "H(10) C(4) N O(2) P"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2013-01-27 13:26:33"
-xref: date_time_modified "2013-02-07 16:50:38"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1365
-name: N-dimethylphosphate
-def: "N-dimethylphosphate." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1365]
-comment: This adduct is a consequence of hydrolysis of the initial adduct formed by tabun (aging) on the active site serine of serine esterases/proteases such as butyrylcholinesterase.
-synonym: "aged tabun" RELATED []
-xref: record_id "1365"
-xref: delta_mono_mass "107.013615"
-xref: delta_avge_mass "107.0483"
-xref: delta_composition "H(6) C(2) N O(2) P"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2013-01-27 13:36:32"
-xref: date_time_modified "2013-02-07 16:49:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1367
-name: dHex(1)Hex(1)
-def: "Hex1dHex1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1367]
-xref: record_id "1367"
-xref: delta_mono_mass "308.110732"
-xref: delta_avge_mass "308.2818"
-xref: delta_composition "dHex Hex"
-xref: username_of_poster "dfplazag"
-xref: group_of_poster ""
-xref: date_time_posted "2013-02-07 14:29:21"
-xref: date_time_modified "2015-05-01 15:14:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_309_mono_mass "308.110732"
-xref: spec_1_neutral_loss_309_avge_mass "308.2818"
-xref: spec_1_neutral_loss_309_flag "false"
-xref: spec_1_neutral_loss_309_composition "dHex Hex"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_309_mono_mass "308.110732"
-xref: spec_1_neutral_loss_309_avge_mass "308.2818"
-xref: spec_1_neutral_loss_309_flag "false"
-xref: spec_1_neutral_loss_309_composition "dHex Hex"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1368
-name: Methyl:2H(3)+Acetyl:2H(3)
-def: "3-fold methylated lysine labelled with Acetyl_heavy." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1368]
-xref: record_id "1368"
-xref: delta_mono_mass "62.063875"
-xref: delta_avge_mass "62.1002"
-xref: delta_composition "H(-2) 2H(6) C(3) O"
-xref: username_of_poster "Plank"
-xref: group_of_poster ""
-xref: date_time_posted "2013-02-14 16:21:54"
-xref: date_time_modified "2013-02-14 16:21:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1370
-name: Label:2H(3)+Oxidation
-def: "Oxidised 2H(3) labelled Methionine." [URL:http\://www.pil.sdu.dk/silac_intro.htm, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1370]
-synonym: "SILAC" RELATED []
-xref: record_id "1370"
-xref: delta_mono_mass "19.013745"
-xref: delta_avge_mass "19.0179"
-xref: delta_composition "H(-3) 2H(3) O"
-xref: username_of_poster "Plank"
-xref: group_of_poster ""
-xref: date_time_posted "2013-02-14 16:36:56"
-xref: date_time_modified "2013-02-22 12:39:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1371
-name: Trimethyl:2H(9)
-def: "3-fold methylation with deuterated methyl groups." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1371]
-xref: record_id "1371"
-xref: delta_mono_mass "51.103441"
-xref: delta_avge_mass "51.1352"
-xref: delta_composition "H(-3) 2H(9) C(3)"
-xref: username_of_poster "Plank"
-xref: group_of_poster ""
-xref: date_time_posted "2013-02-14 17:14:16"
-xref: date_time_modified "2013-02-22 12:37:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "R"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1372
-name: Acetyl:13C(2)
-def: "Heavy acetylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1372]
-xref: record_id "1372"
-xref: delta_mono_mass "44.017274"
-xref: delta_avge_mass "44.022"
-xref: delta_composition "H(2) 13C(2) O"
-xref: username_of_poster "Plank"
-xref: group_of_poster ""
-xref: date_time_posted "2013-02-14 17:24:23"
-xref: date_time_modified "2013-02-14 17:24:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1375
-name: dHex(1)Hex(2)
-def: "Hex2dHex1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1375]
-xref: record_id "1375"
-xref: delta_mono_mass "470.163556"
-xref: delta_avge_mass "470.4224"
-xref: delta_composition "dHex Hex(2)"
-xref: username_of_poster "dfplazag"
-xref: group_of_poster ""
-xref: date_time_posted "2013-04-10 14:57:30"
-xref: date_time_modified "2015-05-01 15:18:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_471_mono_mass "470.163556"
-xref: spec_1_neutral_loss_471_avge_mass "470.4224"
-xref: spec_1_neutral_loss_471_flag "false"
-xref: spec_1_neutral_loss_471_composition "dHex Hex(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_471_mono_mass "470.163556"
-xref: spec_1_neutral_loss_471_avge_mass "470.4224"
-xref: spec_1_neutral_loss_471_flag "false"
-xref: spec_1_neutral_loss_471_composition "dHex Hex(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1376
-name: dHex(1)Hex(3)
-def: "Hex3dHex1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1376]
-xref: record_id "1376"
-xref: delta_mono_mass "632.216379"
-xref: delta_avge_mass "632.563"
-xref: delta_composition "dHex Hex(3)"
-xref: username_of_poster "dfplazag"
-xref: group_of_poster ""
-xref: date_time_posted "2013-04-10 15:00:23"
-xref: date_time_modified "2015-05-01 15:24:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_633_mono_mass "632.216379"
-xref: spec_1_neutral_loss_633_avge_mass "632.563"
-xref: spec_1_neutral_loss_633_flag "false"
-xref: spec_1_neutral_loss_633_composition "dHex Hex(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_633_mono_mass "632.216379"
-xref: spec_1_neutral_loss_633_avge_mass "632.563"
-xref: spec_1_neutral_loss_633_flag "false"
-xref: spec_1_neutral_loss_633_composition "dHex Hex(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1377
-name: dHex(1)Hex(4)
-def: "Hex4dHex1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1377]
-xref: record_id "1377"
-xref: delta_mono_mass "794.269203"
-xref: delta_avge_mass "794.7036"
-xref: delta_composition "dHex Hex(4)"
-xref: username_of_poster "dfplazag"
-xref: group_of_poster ""
-xref: date_time_posted "2013-04-10 15:01:35"
-xref: date_time_modified "2015-05-01 15:27:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_795_mono_mass "794.269203"
-xref: spec_1_neutral_loss_795_avge_mass "794.7036"
-xref: spec_1_neutral_loss_795_flag "false"
-xref: spec_1_neutral_loss_795_composition "dHex Hex(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_795_mono_mass "794.269203"
-xref: spec_1_neutral_loss_795_avge_mass "794.7036"
-xref: spec_1_neutral_loss_795_flag "false"
-xref: spec_1_neutral_loss_795_composition "dHex Hex(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1378
-name: dHex(1)Hex(5)
-def: "Hex5dHex1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1378]
-xref: record_id "1378"
-xref: delta_mono_mass "956.322026"
-xref: delta_avge_mass "956.8442"
-xref: delta_composition "dHex Hex(5)"
-xref: username_of_poster "dfplazag"
-xref: group_of_poster ""
-xref: date_time_posted "2013-04-10 15:03:12"
-xref: date_time_modified "2015-05-01 15:43:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_957_mono_mass "956.322026"
-xref: spec_1_neutral_loss_957_avge_mass "956.8442"
-xref: spec_1_neutral_loss_957_flag "false"
-xref: spec_1_neutral_loss_957_composition "dHex Hex(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_957_mono_mass "956.322026"
-xref: spec_1_neutral_loss_957_avge_mass "956.8442"
-xref: spec_1_neutral_loss_957_flag "false"
-xref: spec_1_neutral_loss_957_composition "dHex Hex(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1379
-name: dHex(1)Hex(6)
-def: "Hex6dHex1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=6&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1379]
-xref: record_id "1379"
-xref: delta_mono_mass "1118.37485"
-xref: delta_avge_mass "1118.9848"
-xref: delta_composition "dHex Hex(6)"
-xref: username_of_poster "dfplazag"
-xref: group_of_poster ""
-xref: date_time_posted "2013-04-10 15:04:22"
-xref: date_time_modified "2015-05-01 15:44:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1119_mono_mass "1118.37485"
-xref: spec_1_neutral_loss_1119_avge_mass "1118.9848"
-xref: spec_1_neutral_loss_1119_flag "false"
-xref: spec_1_neutral_loss_1119_composition "dHex Hex(6)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1119_mono_mass "1118.37485"
-xref: spec_1_neutral_loss_1119_avge_mass "1118.9848"
-xref: spec_1_neutral_loss_1119_flag "false"
-xref: spec_1_neutral_loss_1119_composition "dHex Hex(6)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1380
-name: methylsulfonylethyl
-def: "Reaction with methyl vinyl sulfone." [PMID:http://www.ncbi.nlm.nih.gov/pubmed/?term=2475130, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1380]
-synonym: "protein alkylation by Michael acceptor methyl vinyl sulfone" RELATED []
-xref: record_id "1380"
-xref: delta_mono_mass "106.00885"
-xref: delta_avge_mass "106.1435"
-xref: delta_composition "H(6) C(3) O(2) S"
-xref: username_of_poster "Kramerh"
-xref: group_of_poster ""
-xref: date_time_posted "2013-04-24 14:30:59"
-xref: date_time_modified "2013-05-02 10:13:32"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1381
-name: ethylsulfonylethyl
-def: "Reaction with ethyl vinyl sulfone." [PMID:http://www.ncbi.nlm.nih.gov/pubmed/2475130, PMID:http://www.ncbi.nlm.nih.gov/pubmed/1242713, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1381]
-synonym: "protein alkylation by Michael acceptor ethyl vinyl sulfone" RELATED []
-xref: record_id "1381"
-xref: delta_mono_mass "120.0245"
-xref: delta_avge_mass "120.1701"
-xref: delta_composition "H(8) C(4) O(2) S"
-xref: username_of_poster "Kramerh"
-xref: group_of_poster ""
-xref: date_time_posted "2013-04-24 14:36:48"
-xref: date_time_modified "2013-04-26 09:25:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1382
-name: phenylsulfonylethyl
-def: "Reaction with phenyl vinyl sulfone." [PMID:http://www.ncbi.nlm.nih.gov/pubmed/18528979, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1382]
-synonym: "protein alkylation by Michael acceptor phenyl vinyl sulfone" RELATED []
-xref: record_id "1382"
-xref: delta_mono_mass "168.0245"
-xref: delta_avge_mass "168.2129"
-xref: delta_composition "H(8) C(8) O(2) S"
-xref: username_of_poster "Kramerh"
-xref: group_of_poster ""
-xref: date_time_posted "2013-04-24 14:41:29"
-xref: date_time_modified "2013-04-26 09:25:21"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1383
-name: PyridoxalPhosphateH2
-def: "PLP bound to lysine reduced by sodium borohydride (NaBH4) to create amine linkage." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1383]
-synonym: "Pyridoxal Phosphate reduced" RELATED []
-xref: record_id "1383"
-xref: delta_mono_mass "231.02966"
-xref: delta_avge_mass "231.1425"
-xref: delta_composition "H(10) C(8) N O(5) P"
-xref: username_of_poster "bphilmus"
-xref: group_of_poster ""
-xref: date_time_posted "2013-04-29 17:33:45"
-xref: date_time_modified "2013-05-03 17:30:38"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "This is a chemical derivatization of the PLP imine with sodium borohydride to reduce imine bound through lysine epsilon amine group to chemical stable amine linkage"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1384
-name: Homocysteic_acid
-def: "Methionine oxidation to homocysteic acid." [PMID:20169556, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1384]
-xref: record_id "1384"
-xref: delta_mono_mass "33.969094"
-xref: delta_avge_mass "33.9716"
-xref: delta_composition "H(-2) C(-1) O(3)"
-xref: username_of_poster "mbern"
-xref: group_of_poster ""
-xref: date_time_posted "2013-05-16 20:08:11"
-xref: date_time_modified "2013-05-31 15:57:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1385
-name: Hydroxamic_acid
-def: "ADP-ribosylation followed by conversion to hydroxamic acid via hydroxylamine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1385]
-synonym: "Conversion of carboxylic acid to hydroxamic acid" RELATED []
-xref: record_id "1385"
-xref: delta_mono_mass "15.010899"
-xref: delta_avge_mass "15.0146"
-xref: delta_composition "H N"
-xref: username_of_poster "mbern"
-xref: group_of_poster ""
-xref: date_time_posted "2013-05-16 20:40:47"
-xref: date_time_modified "2020-03-26 09:49:42"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_misc_notes "From exposure to hydroxylamine (used with TMT)"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_misc_notes "From exposure to hydroxylamine (used with TMT)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1387
-name: 3-phosphoglyceryl
-def: "3-phosphoglyceryl." [PMID:http://www.ncbi.nlm.nih.gov/pubmed/?term=23908237, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1387]
-xref: record_id "1387"
-xref: delta_mono_mass "167.982375"
-xref: delta_avge_mass "168.042"
-xref: delta_composition "H(5) C(3) O(6) P"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2013-08-05 10:54:22"
-xref: date_time_modified "2013-11-01 16:34:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1388
-name: HN2_mustard
-def: "Modification by hydroxylated mechloroethamine (HN-2)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1388]
-xref: record_id "1388"
-xref: delta_mono_mass "101.084064"
-xref: delta_avge_mass "101.1469"
-xref: delta_composition "H(11) C(5) N O"
-xref: username_of_poster "vthompson"
-xref: group_of_poster ""
-xref: date_time_posted "2013-08-23 18:36:39"
-xref: date_time_modified "2013-09-23 11:42:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1389
-name: HN3_mustard
-def: "Modification by hydroxylated tris-(2-chloroethyl)amine (HN-3)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1389]
-xref: record_id "1389"
-xref: delta_mono_mass "131.094629"
-xref: delta_avge_mass "131.1729"
-xref: delta_composition "H(13) C(6) N O(2)"
-xref: username_of_poster "vthompson"
-xref: group_of_poster ""
-xref: date_time_posted "2013-08-23 19:13:36"
-xref: date_time_modified "2013-09-23 11:42:08"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1390
-name: Oxidation+NEM
-def: "N-ethylmaleimide on cysteine sulfenic acid." [PMID:24103186, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1390]
-xref: record_id "1390"
-xref: delta_mono_mass "141.042593"
-xref: delta_avge_mass "141.1247"
-xref: delta_composition "H(7) C(6) N O(3)"
-xref: username_of_poster "jheld"
-xref: group_of_poster ""
-xref: date_time_posted "2013-10-16 15:31:20"
-xref: date_time_modified "2013-11-01 16:37:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1391
-name: NHS-fluorescein
-def: "Fluorescein-hexanoate-NHS hydrolysis." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1391]
-xref: record_id "1391"
-xref: delta_mono_mass "471.131802"
-xref: delta_avge_mass "471.4581"
-xref: delta_composition "H(21) C(27) N O(7)"
-xref: username_of_poster "cgadelha"
-xref: group_of_poster ""
-xref: date_time_posted "2013-10-18 12:14:19"
-xref: date_time_modified "2013-11-01 16:37:42"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1392
-name: DiART6plex
-def: "Representative mass and accurate mass for 114." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1392]
-comment: Different tags have the same nominal mass but slightly different exact masses. Use this modification for all tags for quantitation purposes. Monoisotopic masses of the fragment ions to be quantified are 114.12827, 115.12531, 116.14082, 117.13786, 118.14752, 119.14456.
-synonym: "Isobaric labeling reagent from Omic Biosystems, Inc. AKA DiART6plex114" RELATED []
-xref: record_id "1392"
-xref: delta_mono_mass "217.162932"
-xref: delta_avge_mass "217.2527"
-xref: delta_composition "H(20) C(7) 13C(4) N 15N O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2013-11-06 11:18:58"
-xref: date_time_modified "2016-09-22 14:39:36"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Isotopic label"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "Y"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "Low abundance"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1393
-name: DiART6plex115
-def: "Accurate mass for DiART6plex 115." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1393]
-comment: Different tags have the same nominal mass but slightly different exact masses.
-synonym: "Isobaric labeling reagent from Omic Biosystems, Inc." RELATED []
-xref: record_id "1393"
-xref: delta_mono_mass "217.156612"
-xref: delta_avge_mass "217.2535"
-xref: delta_composition "H(20) C(8) 13C(3) 15N(2) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2013-11-06 11:34:33"
-xref: date_time_modified "2013-11-06 11:34:33"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Isotopic label"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "Y"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "Low abundance"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1394
-name: DiART6plex116/119
-def: "Accurate mass for DiART6plex 116 and 119." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1394]
-comment: Different tags have the same nominal mass but slightly different exact masses.
-synonym: "Isobaric labeling reagent from Omic Biosystems, Inc." RELATED []
-xref: record_id "1394"
-xref: delta_mono_mass "217.168776"
-xref: delta_avge_mass "217.2797"
-xref: delta_composition "H(18) 2H(2) C(9) 13C(2) N 15N O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2013-11-06 11:35:52"
-xref: date_time_modified "2013-11-06 11:38:53"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Isotopic label"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "Y"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "Low abundance"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1395
-name: DiART6plex117
-def: "Accurate mass for DiART6plex 117." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1395]
-comment: Different tags have the same nominal mass but slightly different exact masses.
-synonym: "Isobaric labeling reagent from Omic Biosystems, Inc." RELATED []
-xref: record_id "1395"
-xref: delta_mono_mass "217.162456"
-xref: delta_avge_mass "217.2805"
-xref: delta_composition "H(18) 2H(2) C(10) 13C 15N(2) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2013-11-06 11:40:01"
-xref: date_time_modified "2013-11-06 11:40:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Isotopic label"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "Y"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "Low abundance"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1396
-name: DiART6plex118
-def: "Accurate mass for DiART6plex 118." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1396]
-comment: Different tags have the same nominal mass but slightly different exact masses.
-synonym: "Isobaric labeling reagent from Omic Biosystems, Inc." RELATED []
-xref: record_id "1396"
-xref: delta_mono_mass "217.175096"
-xref: delta_avge_mass "217.279"
-xref: delta_composition "H(18) 2H(2) C(8) 13C(3) N(2) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2013-11-06 11:40:58"
-xref: date_time_modified "2013-11-06 11:40:58"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Isotopic label"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "Y"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "Low abundance"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1397
-name: Iodoacetanilide
-def: "Iodoacetanilide derivative." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1397]
-xref: record_id "1397"
-xref: delta_mono_mass "133.052764"
-xref: delta_avge_mass "133.1473"
-xref: delta_composition "H(7) C(8) N O"
-xref: username_of_poster "kcook123"
-xref: group_of_poster ""
-xref: date_time_posted "2013-12-10 04:26:07"
-xref: date_time_modified "2014-03-01 17:35:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1398
-name: Iodoacetanilide:13C(6)
-def: "13C labelled iodoacetanilide derivative." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1398]
-xref: record_id "1398"
-xref: delta_mono_mass "139.072893"
-xref: delta_avge_mass "139.1032"
-xref: delta_composition "H(7) C(2) 13C(6) N O"
-xref: username_of_poster "kcook123"
-xref: group_of_poster ""
-xref: date_time_posted "2013-12-10 04:31:00"
-xref: date_time_modified "2014-03-01 17:36:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1399
-name: Dap-DSP
-def: "Diaminopimelic acid-DSP monolinked." [URL:https\://tools.thermofisher.com/content/sfs/manuals/MAN0011280_DTSSP_DSP_UG.pdf, URL:https\://www.ncbi.nlm.nih.gov/pubmed/?term=322714, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1399]
-comment: Addition of gram negative peptidoglycan amino acid (DAP) plus monolinked DSP.
-xref: record_id "1399"
-xref: delta_mono_mass "364.076278"
-xref: delta_avge_mass "364.4377"
-xref: delta_composition "H(20) C(13) N(2) O(6) S(2)"
-xref: username_of_poster "grigorios"
-xref: group_of_poster ""
-xref: date_time_posted "2014-02-20 11:23:24"
-xref: date_time_modified "2017-09-19 11:06:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Non-standard residue"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "E"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Non-standard residue"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1400
-name: MurNAc
-def: "N-Acetylmuramic acid." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1400]
-comment: Gram negative peptidoglycan saccharide amide bonded to Alanine.
-xref: record_id "1400"
-xref: delta_mono_mass "275.100502"
-xref: delta_avge_mass "275.2552"
-xref: delta_composition "O(-1) NeuAc"
-xref: username_of_poster "grigorios"
-xref: group_of_poster ""
-xref: date_time_posted "2014-02-20 12:47:46"
-xref: date_time_modified "2015-05-01 13:37:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other glycosylation"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1402
-name: Label:2H(7)15N(4)
-def: "Label:2H(7)15N(4)." [URL:http\://shop.isotope.com/productdetails.aspx?id=10032309&itemno=DNLM-7543-PK, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1402]
-comment: For SILAC experiments.
-synonym: "Cambridge Isotopes DNLM-7543-PK" RELATED []
-xref: record_id "1402"
-xref: delta_mono_mass "11.032077"
-xref: delta_avge_mass "11.0168"
-xref: delta_composition "H(-7) 2H(7) N(-4) 15N(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2014-04-16 12:16:45"
-xref: date_time_modified "2014-04-16 12:16:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1403
-name: Label:2H(6)15N(1)
-def: "Label:2H(6)15N(1)." [URL:http\://shop.isotope.com/productdetails.aspx?id=10032309&itemno=DNLM-7543-PK, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1403]
-comment: For SILAC experiments.
-synonym: "Arg-Pro conversion of Label:2H(7)15N(4)" RELATED []
-xref: record_id "1403"
-xref: delta_mono_mass "7.034695"
-xref: delta_avge_mass "7.0304"
-xref: delta_composition "H(-6) 2H(6) N(-1) 15N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2014-04-16 12:19:06"
-xref: date_time_modified "2014-04-16 12:19:06"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1405
-name: EEEDVIEVYQEQTGG
-def: "Sumoylation by SUMO-1 after Cyanogen bromide (CNBr) cleavage." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1405]
-xref: record_id "1405"
-xref: delta_mono_mass "1705.73189"
-xref: delta_avge_mass "1706.7153"
-xref: delta_composition "H(107) C(72) N(17) O(31)"
-xref: username_of_poster "vogelw"
-xref: group_of_poster ""
-xref: date_time_posted "2014-06-25 15:15:44"
-xref: date_time_modified "2014-08-08 11:37:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1406
-name: EDEDTIDVFQQQTGG
-def: "Sumoylation by SUMO-2/3 after Cyanogen bromide (CNBr) cleavage." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1406]
-xref: record_id "1406"
-xref: delta_mono_mass "1662.700924"
-xref: delta_avge_mass "1663.6508"
-xref: delta_composition "H(102) C(69) N(18) O(30)"
-xref: username_of_poster "vogelw"
-xref: group_of_poster ""
-xref: date_time_posted "2014-06-25 15:19:11"
-xref: date_time_modified "2014-08-08 11:37:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "The cleavage products of SUMO-2 and SUMO-3 are indistinguishable"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1408
-name: Hex(5)HexNAc(4)NeuAc(2)
-def: "A2G2S2/G2S2." [URL:http\://www.unicarbkb.org/structure/1187, URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=5&hexnac=4&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1408]
-xref: record_id "1408"
-xref: delta_mono_mass "2204.772441"
-xref: delta_avge_mass "2205.9822"
-xref: delta_composition "Hex(5) HexNAc(4) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2014-07-31 13:51:41"
-xref: date_time_modified "2020-08-02 11:36:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_2205_mono_mass "2204.772441"
-xref: spec_1_neutral_loss_2205_avge_mass "2205.9822"
-xref: spec_1_neutral_loss_2205_flag "false"
-xref: spec_1_neutral_loss_2205_composition "Hex(5) HexNAc(4) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1409
-name: Hex(5)HexNAc(4)NeuAc(1)
-def: "A2G2S1/G2S1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=5&hexnac=4&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1409]
-xref: record_id "1409"
-xref: delta_mono_mass "1913.677025"
-xref: delta_avge_mass "1914.7277"
-xref: delta_composition "Hex(5) HexNAc(4) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2014-07-31 13:52:20"
-xref: date_time_modified "2020-08-02 11:37:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1914_mono_mass "1913.677025"
-xref: spec_1_neutral_loss_1914_avge_mass "1914.7277"
-xref: spec_1_neutral_loss_1914_flag "false"
-xref: spec_1_neutral_loss_1914_composition "Hex(5) HexNAc(4) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1410
-name: dHex(1)Hex(5)HexNAc(4)NeuAc(1)
-def: "FA2G2S1/G2FS1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=5&hexnac=4&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1410]
-xref: record_id "1410"
-xref: delta_mono_mass "2059.734933"
-xref: delta_avge_mass "2060.8689"
-xref: delta_composition "dHex Hex(5) HexNAc(4) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2014-07-31 13:53:31"
-xref: date_time_modified "2020-08-02 11:40:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_2060_mono_mass "2059.734933"
-xref: spec_1_neutral_loss_2060_avge_mass "2060.8689"
-xref: spec_1_neutral_loss_2060_flag "false"
-xref: spec_1_neutral_loss_2060_composition "dHex Hex(5) HexNAc(4) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1411
-name: dHex(1)Hex(5)HexNAc(4)NeuAc(2)
-def: "FA2G2S2/G2FS2." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=5&hexnac=4&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1411]
-xref: record_id "1411"
-xref: delta_mono_mass "2350.83035"
-xref: delta_avge_mass "2352.1234"
-xref: delta_composition "dHex Hex(5) HexNAc(4) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2014-07-31 13:53:47"
-xref: date_time_modified "2020-08-02 11:40:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_2351_mono_mass "2350.83035"
-xref: spec_1_neutral_loss_2351_avge_mass "2352.1234"
-xref: spec_1_neutral_loss_2351_flag "false"
-xref: spec_1_neutral_loss_2351_composition "dHex Hex(5) HexNAc(4) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1412
-name: s-GlcNAc
-def: "O3S1HexNAc1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1412]
-xref: record_id "1412"
-xref: delta_mono_mass "283.036187"
-xref: delta_avge_mass "283.2557"
-xref: delta_composition "O(3) S HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2014-08-14 15:34:42"
-xref: date_time_modified "2015-05-01 15:10:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_284_mono_mass "283.036187"
-xref: spec_1_neutral_loss_284_avge_mass "283.2557"
-xref: spec_1_neutral_loss_284_flag "false"
-xref: spec_1_neutral_loss_284_composition "O(3) S HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_284_mono_mass "283.036187"
-xref: spec_1_neutral_loss_284_avge_mass "283.2557"
-xref: spec_1_neutral_loss_284_flag "false"
-xref: spec_1_neutral_loss_284_composition "O(3) S HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1413
-name: PhosphoHex(2)
-def: "H1O3P1Hex2." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=1&hex=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1413]
-xref: record_id "1413"
-xref: delta_mono_mass "404.071978"
-xref: delta_avge_mass "404.2611"
-xref: delta_composition "H O(3) P Hex(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2014-08-14 15:38:35"
-xref: date_time_modified "2017-11-23 15:44:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_405_mono_mass "404.071978"
-xref: spec_1_neutral_loss_405_avge_mass "404.2611"
-xref: spec_1_neutral_loss_405_flag "false"
-xref: spec_1_neutral_loss_405_composition "H O(3) P Hex(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_405_mono_mass "404.071978"
-xref: spec_1_neutral_loss_405_avge_mass "404.2611"
-xref: spec_1_neutral_loss_405_flag "false"
-xref: spec_1_neutral_loss_405_composition "H O(3) P Hex(2)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_misc_notes "Not reported for human proteins"
-xref: spec_2_neutral_loss_405_mono_mass "404.071978"
-xref: spec_2_neutral_loss_405_avge_mass "404.2611"
-xref: spec_2_neutral_loss_405_flag "false"
-xref: spec_2_neutral_loss_405_composition "H O(3) P Hex(2)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1414
-name: Trimethyl:13C(3)2H(9)
-def: "3-fold methylation with fully labelled methyl groups." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1414]
-xref: record_id "1414"
-xref: delta_mono_mass "54.113505"
-xref: delta_avge_mass "54.1132"
-xref: delta_composition "H(-3) 2H(9) 13C(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2014-09-17 09:18:49"
-xref: date_time_modified "2014-09-17 09:18:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "R"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1419
-name: 15N-oxobutanoic
-def: "Loss of ammonia (15N)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1419]
-synonym: "pyruvic acid from N-term ser oxobutanoic acid from N term Thr" RELATED []
-xref: record_id "1419"
-xref: delta_mono_mass "-18.023584"
-xref: delta_avge_mass "-18.0239"
-xref: delta_composition "H(-3) 15N(-1)"
-xref: username_of_poster "fufezan"
-xref: group_of_poster ""
-xref: date_time_posted "2014-11-24 13:24:53"
-xref: date_time_modified "2015-01-12 16:11:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Artefact"
-xref: spec_1_misc_notes "Pyro-carbamidomethyl as a delta from Carbamidomethyl-Cys"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1420
-name: spermine
-def: "Spermine adduct." [URL:http\://dx.doi.org/10.1007/s00726-014-1879-8, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1420]
-xref: record_id "1420"
-xref: delta_mono_mass "185.189198"
-xref: delta_avge_mass "185.3097"
-xref: delta_composition "H(23) C(10) N(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-01-12 16:07:00"
-xref: date_time_modified "2024-08-12 10:11:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1421
-name: spermidine
-def: "Spermidine adduct." [URL:http\://dx.doi.org/10.1007/s00726-014-1879-8, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1421]
-xref: record_id "1421"
-xref: delta_mono_mass "128.131349"
-xref: delta_avge_mass "128.2153"
-xref: delta_composition "H(16) C(7) N(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-01-12 16:08:04"
-xref: date_time_modified "2024-08-12 10:11:10"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1423
-name: Biotin:Thermo-21330
-def: "Biotin_PEG4." [URL:http\://www.lifetechnologies.com/order/catalog/product/21330, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1423]
-comment: Also available as 21329, 21362, 21363.
-synonym: "NHS-PEG4-Biotin" RELATED []
-xref: record_id "1423"
-xref: delta_mono_mass "473.219571"
-xref: delta_avge_mass "473.5835"
-xref: delta_composition "H(35) C(21) N(3) O(7) S"
-xref: username_of_poster "rbomgard"
-xref: group_of_poster ""
-xref: date_time_posted "2015-04-20 16:08:05"
-xref: date_time_modified "2015-04-20 16:10:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1425
-name: Pentose
-def: "Pentose." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1425]
-xref: record_id "1425"
-xref: delta_mono_mass "132.042259"
-xref: delta_avge_mass "132.1146"
-xref: delta_composition "Pent"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-01 17:01:09"
-xref: date_time_modified "2015-05-05 10:48:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_133_mono_mass "132.042259"
-xref: spec_1_neutral_loss_133_avge_mass "132.1146"
-xref: spec_1_neutral_loss_133_flag "false"
-xref: spec_1_neutral_loss_133_composition "Pent"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_133_mono_mass "132.042259"
-xref: spec_1_neutral_loss_133_avge_mass "132.1146"
-xref: spec_1_neutral_loss_133_flag "false"
-xref: spec_1_neutral_loss_133_composition "Pent"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1426
-name: Hex(1)Pent(1)
-def: "Hex Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?pent=1&hex=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1426]
-xref: record_id "1426"
-xref: delta_mono_mass "294.095082"
-xref: delta_avge_mass "294.2552"
-xref: delta_composition "Pent Hex"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-01 17:03:00"
-xref: date_time_modified "2015-05-05 10:49:06"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_295_mono_mass "294.095082"
-xref: spec_1_neutral_loss_295_avge_mass "294.2552"
-xref: spec_1_neutral_loss_295_flag "false"
-xref: spec_1_neutral_loss_295_composition "Pent Hex"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_295_mono_mass "294.095082"
-xref: spec_1_neutral_loss_295_avge_mass "294.2552"
-xref: spec_1_neutral_loss_295_flag "false"
-xref: spec_1_neutral_loss_295_composition "Pent Hex"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1427
-name: Hex(1)HexA(1)
-def: "Hex HexA." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexa=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1427]
-xref: record_id "1427"
-xref: delta_mono_mass "338.084912"
-xref: delta_avge_mass "338.2647"
-xref: delta_composition "Hex HexA"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-01 17:05:51"
-xref: date_time_modified "2015-05-05 10:49:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_339_mono_mass "338.084912"
-xref: spec_1_neutral_loss_339_avge_mass "338.2647"
-xref: spec_1_neutral_loss_339_flag "false"
-xref: spec_1_neutral_loss_339_composition "Hex HexA"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_339_mono_mass "338.084912"
-xref: spec_1_neutral_loss_339_avge_mass "338.2647"
-xref: spec_1_neutral_loss_339_flag "false"
-xref: spec_1_neutral_loss_339_composition "Hex HexA"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1428
-name: Hex(1)Pent(2)
-def: "Hex Pent(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?pent=2&hex=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1428]
-xref: record_id "1428"
-xref: delta_mono_mass "426.137341"
-xref: delta_avge_mass "426.3698"
-xref: delta_composition "Pent(2) Hex"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 09:37:19"
-xref: date_time_modified "2015-05-05 10:50:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_427_mono_mass "426.137341"
-xref: spec_1_neutral_loss_427_avge_mass "426.3698"
-xref: spec_1_neutral_loss_427_flag "false"
-xref: spec_1_neutral_loss_427_composition "Pent(2) Hex"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_427_mono_mass "426.137341"
-xref: spec_1_neutral_loss_427_avge_mass "426.3698"
-xref: spec_1_neutral_loss_427_flag "false"
-xref: spec_1_neutral_loss_427_composition "Pent(2) Hex"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1429
-name: Hex(1)HexNAc(1)Phos(1)
-def: "Hex HexNAc Phos." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=1&hex=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1429]
-xref: record_id "1429"
-xref: delta_mono_mass "445.098527"
-xref: delta_avge_mass "445.313"
-xref: delta_composition "H O(3) P Hex HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 09:40:49"
-xref: date_time_modified "2015-05-06 12:07:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_446_mono_mass "445.098527"
-xref: spec_1_neutral_loss_446_avge_mass "445.313"
-xref: spec_1_neutral_loss_446_flag "false"
-xref: spec_1_neutral_loss_446_composition "H O(3) P Hex HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_446_mono_mass "445.098527"
-xref: spec_1_neutral_loss_446_avge_mass "445.313"
-xref: spec_1_neutral_loss_446_flag "false"
-xref: spec_1_neutral_loss_446_composition "H O(3) P Hex HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1430
-name: Hex(1)HexNAc(1)Sulf(1)
-def: "Hex HexNAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1430]
-xref: record_id "1430"
-xref: delta_mono_mass "445.089011"
-xref: delta_avge_mass "445.3963"
-xref: delta_composition "O(3) S Hex HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 09:41:48"
-xref: date_time_modified "2015-05-06 12:07:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_446_mono_mass "445.089011"
-xref: spec_1_neutral_loss_446_avge_mass "445.3963"
-xref: spec_1_neutral_loss_446_flag "false"
-xref: spec_1_neutral_loss_446_composition "O(3) S Hex HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_446_mono_mass "445.089011"
-xref: spec_1_neutral_loss_446_avge_mass "445.3963"
-xref: spec_1_neutral_loss_446_flag "false"
-xref: spec_1_neutral_loss_446_composition "O(3) S Hex HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1431
-name: Hex(1)NeuAc(1)
-def: "Hex NeuAc ---OR--- HexNAc Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1431]
-xref: record_id "1431"
-xref: delta_mono_mass "453.14824"
-xref: delta_avge_mass "453.3952"
-xref: delta_composition "Hex NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 09:45:11"
-xref: date_time_modified "2017-11-17 11:42:48"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_454_mono_mass "453.14824"
-xref: spec_1_neutral_loss_454_avge_mass "453.3952"
-xref: spec_1_neutral_loss_454_flag "false"
-xref: spec_1_neutral_loss_454_composition "Hex NeuAc"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_454_mono_mass "453.14824"
-xref: spec_1_neutral_loss_454_avge_mass "453.3952"
-xref: spec_1_neutral_loss_454_flag "false"
-xref: spec_1_neutral_loss_454_composition "Hex NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1432
-name: Hex(1)NeuGc(1)
-def: "Hex NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1432]
-xref: record_id "1432"
-xref: delta_mono_mass "469.143155"
-xref: delta_avge_mass "469.3946"
-xref: delta_composition "Hex NeuGc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 09:45:57"
-xref: date_time_modified "2015-05-05 10:51:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_470_mono_mass "469.143155"
-xref: spec_1_neutral_loss_470_avge_mass "469.3946"
-xref: spec_1_neutral_loss_470_flag "false"
-xref: spec_1_neutral_loss_470_composition "Hex NeuGc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_470_mono_mass "469.143155"
-xref: spec_1_neutral_loss_470_avge_mass "469.3946"
-xref: spec_1_neutral_loss_470_flag "false"
-xref: spec_1_neutral_loss_470_composition "Hex NeuGc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1433
-name: HexNAc(3)
-def: "HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1433]
-xref: record_id "1433"
-xref: delta_mono_mass "609.238118"
-xref: delta_avge_mass "609.5776"
-xref: delta_composition "HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 09:47:58"
-xref: date_time_modified "2015-05-06 12:09:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_610_mono_mass "609.238118"
-xref: spec_1_neutral_loss_610_avge_mass "609.5776"
-xref: spec_1_neutral_loss_610_flag "false"
-xref: spec_1_neutral_loss_610_composition "HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_610_mono_mass "609.238118"
-xref: spec_1_neutral_loss_610_avge_mass "609.5776"
-xref: spec_1_neutral_loss_610_flag "false"
-xref: spec_1_neutral_loss_610_composition "HexNAc(3)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1434
-name: HexNAc(1)NeuAc(1)
-def: "HexNAc NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hexnac=1&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1434]
-xref: record_id "1434"
-xref: delta_mono_mass "494.174789"
-xref: delta_avge_mass "494.4471"
-xref: delta_composition "HexNAc NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 09:53:18"
-xref: date_time_modified "2015-05-05 10:52:24"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_495_mono_mass "494.174789"
-xref: spec_1_neutral_loss_495_avge_mass "494.4471"
-xref: spec_1_neutral_loss_495_flag "false"
-xref: spec_1_neutral_loss_495_composition "HexNAc NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_495_mono_mass "494.174789"
-xref: spec_1_neutral_loss_495_avge_mass "494.4471"
-xref: spec_1_neutral_loss_495_flag "false"
-xref: spec_1_neutral_loss_495_composition "HexNAc NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1435
-name: HexNAc(1)NeuGc(1)
-def: "HexNAc NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hexnac=1&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1435]
-xref: record_id "1435"
-xref: delta_mono_mass "510.169704"
-xref: delta_avge_mass "510.4465"
-xref: delta_composition "HexNAc NeuGc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 09:54:16"
-xref: date_time_modified "2015-05-05 10:52:39"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_511_mono_mass "510.169704"
-xref: spec_1_neutral_loss_511_avge_mass "510.4465"
-xref: spec_1_neutral_loss_511_flag "false"
-xref: spec_1_neutral_loss_511_composition "HexNAc NeuGc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_511_mono_mass "510.169704"
-xref: spec_1_neutral_loss_511_avge_mass "510.4465"
-xref: spec_1_neutral_loss_511_flag "false"
-xref: spec_1_neutral_loss_511_composition "HexNAc NeuGc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1436
-name: Hex(1)HexNAc(1)dHex(1)Me(1)
-def: "Hex HexNAc dHex Me." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?methyl=1&dhex=1&hex=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1436]
-xref: record_id "1436"
-xref: delta_mono_mass "525.205755"
-xref: delta_avge_mass "525.5009"
-xref: delta_composition "Me dHex Hex HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 10:05:16"
-xref: date_time_modified "2015-05-06 12:08:10"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_526_mono_mass "525.205755"
-xref: spec_1_neutral_loss_526_avge_mass "525.5009"
-xref: spec_1_neutral_loss_526_flag "false"
-xref: spec_1_neutral_loss_526_composition "Me dHex Hex HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_526_mono_mass "525.205755"
-xref: spec_1_neutral_loss_526_avge_mass "525.5009"
-xref: spec_1_neutral_loss_526_flag "false"
-xref: spec_1_neutral_loss_526_composition "Me dHex Hex HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1437
-name: Hex(1)HexNAc(1)dHex(1)Me(2)
-def: "Hex HexNAc dHex Me(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?methyl=2&dhex=1&hex=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1437]
-xref: record_id "1437"
-xref: delta_mono_mass "539.221405"
-xref: delta_avge_mass "539.5275"
-xref: delta_composition "Me(2) dHex Hex HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 10:06:28"
-xref: date_time_modified "2015-05-06 12:08:43"
-xref: approved "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_540_mono_mass "539.221405"
-xref: spec_2_neutral_loss_540_avge_mass "539.5275"
-xref: spec_2_neutral_loss_540_flag "false"
-xref: spec_2_neutral_loss_540_composition "Me(2) dHex Hex HexNAc"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_540_mono_mass "539.221405"
-xref: spec_2_neutral_loss_540_avge_mass "539.5275"
-xref: spec_2_neutral_loss_540_flag "false"
-xref: spec_2_neutral_loss_540_composition "Me(2) dHex Hex HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1438
-name: Hex(2)HexNAc(1)
-def: "Hex(2) HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1438]
-xref: record_id "1438"
-xref: delta_mono_mass "527.18502"
-xref: delta_avge_mass "527.4737"
-xref: delta_composition "Hex(2) HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 10:09:00"
-xref: date_time_modified "2017-11-23 16:36:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_528_mono_mass "527.18502"
-xref: spec_1_neutral_loss_528_avge_mass "527.4737"
-xref: spec_1_neutral_loss_528_flag "false"
-xref: spec_1_neutral_loss_528_composition "Hex(2) HexNAc"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_528_mono_mass "527.18502"
-xref: spec_1_neutral_loss_528_avge_mass "527.4737"
-xref: spec_1_neutral_loss_528_flag "false"
-xref: spec_1_neutral_loss_528_composition "Hex(2) HexNAc"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_528_mono_mass "527.18502"
-xref: spec_2_neutral_loss_528_avge_mass "527.4737"
-xref: spec_2_neutral_loss_528_flag "false"
-xref: spec_2_neutral_loss_528_composition "Hex(2) HexNAc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1439
-name: Hex(1)HexA(1)HexNAc(1)
-def: "Hex HexA HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexa=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1439]
-xref: record_id "1439"
-xref: delta_mono_mass "541.164284"
-xref: delta_avge_mass "541.4572"
-xref: delta_composition "Hex HexA HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 10:10:30"
-xref: date_time_modified "2015-05-05 10:55:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_542_mono_mass "541.164284"
-xref: spec_1_neutral_loss_542_avge_mass "541.4572"
-xref: spec_1_neutral_loss_542_flag "false"
-xref: spec_1_neutral_loss_542_composition "Hex HexA HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_542_mono_mass "541.164284"
-xref: spec_1_neutral_loss_542_avge_mass "541.4572"
-xref: spec_1_neutral_loss_542_flag "false"
-xref: spec_1_neutral_loss_542_composition "Hex HexA HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1440
-name: Hex(2)HexNAc(1)Me(1)
-def: "Hex(2) HexNAc Me." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?methyl=1&hex=2&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1440]
-xref: record_id "1440"
-xref: delta_mono_mass "541.20067"
-xref: delta_avge_mass "541.5003"
-xref: delta_composition "Me Hex(2) HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 10:12:19"
-xref: date_time_modified "2015-05-06 12:08:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_542_mono_mass "541.20067"
-xref: spec_1_neutral_loss_542_avge_mass "541.5003"
-xref: spec_1_neutral_loss_542_flag "false"
-xref: spec_1_neutral_loss_542_composition "Me Hex(2) HexNAc"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_542_mono_mass "541.20067"
-xref: spec_1_neutral_loss_542_avge_mass "541.5003"
-xref: spec_1_neutral_loss_542_flag "false"
-xref: spec_1_neutral_loss_542_composition "Me Hex(2) HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1441
-name: Hex(1)Pent(3)
-def: "Hex Pent(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?pent=3&hex=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1441]
-xref: record_id "1441"
-xref: delta_mono_mass "558.1796"
-xref: delta_avge_mass "558.4845"
-xref: delta_composition "Pent(3) Hex"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 10:14:37"
-xref: date_time_modified "2017-11-23 16:39:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_559_mono_mass "558.1796"
-xref: spec_1_neutral_loss_559_avge_mass "558.4845"
-xref: spec_1_neutral_loss_559_flag "false"
-xref: spec_1_neutral_loss_559_composition "Pent(3) Hex"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_559_mono_mass "558.1796"
-xref: spec_1_neutral_loss_559_avge_mass "558.4845"
-xref: spec_1_neutral_loss_559_flag "false"
-xref: spec_1_neutral_loss_559_composition "Pent(3) Hex"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1442
-name: Hex(1)NeuAc(1)Pent(1)
-def: "Hex NeuAc Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?pent=1&hex=1&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1442]
-xref: record_id "1442"
-xref: delta_mono_mass "585.190499"
-xref: delta_avge_mass "585.5098"
-xref: delta_composition "Pent Hex NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 10:59:44"
-xref: date_time_modified "2015-05-05 10:59:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_586_mono_mass "585.190499"
-xref: spec_1_neutral_loss_586_avge_mass "585.5098"
-xref: spec_1_neutral_loss_586_flag "false"
-xref: spec_1_neutral_loss_586_composition "Pent Hex NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_586_mono_mass "585.190499"
-xref: spec_1_neutral_loss_586_avge_mass "585.5098"
-xref: spec_1_neutral_loss_586_flag "false"
-xref: spec_1_neutral_loss_586_composition "Pent Hex NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1443
-name: Hex(2)HexNAc(1)Sulf(1)
-def: "Hex(2) HexNAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=2&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1443]
-xref: record_id "1443"
-xref: delta_mono_mass "607.141834"
-xref: delta_avge_mass "607.5369"
-xref: delta_composition "O(3) S Hex(2) HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 11:01:43"
-xref: date_time_modified "2015-05-06 12:09:15"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_608_mono_mass "607.141834"
-xref: spec_1_neutral_loss_608_avge_mass "607.5369"
-xref: spec_1_neutral_loss_608_flag "false"
-xref: spec_1_neutral_loss_608_composition "O(3) S Hex(2) HexNAc"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_608_mono_mass "607.141834"
-xref: spec_1_neutral_loss_608_avge_mass "607.5369"
-xref: spec_1_neutral_loss_608_flag "false"
-xref: spec_1_neutral_loss_608_composition "O(3) S Hex(2) HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1444
-name: Hex(2)NeuAc(1)
-def: "Hex(2) NeuAc ---OR--- Hex HexNAc Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1444]
-xref: record_id "1444"
-xref: delta_mono_mass "615.201064"
-xref: delta_avge_mass "615.5358"
-xref: delta_composition "Hex(2) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 11:04:03"
-xref: date_time_modified "2017-11-17 11:43:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_616_mono_mass "615.201064"
-xref: spec_1_neutral_loss_616_avge_mass "615.5358"
-xref: spec_1_neutral_loss_616_flag "false"
-xref: spec_1_neutral_loss_616_composition "Hex(2) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_616_mono_mass "615.201064"
-xref: spec_1_neutral_loss_616_avge_mass "615.5358"
-xref: spec_1_neutral_loss_616_flag "false"
-xref: spec_1_neutral_loss_616_composition "Hex(2) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1445
-name: dHex(2)Hex(2)
-def: "Hex2 dHex2." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1445]
-xref: record_id "1445"
-xref: delta_mono_mass "616.221465"
-xref: delta_avge_mass "616.5636"
-xref: delta_composition "dHex(2) Hex(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 11:05:19"
-xref: date_time_modified "2015-05-05 11:05:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_617_mono_mass "616.221465"
-xref: spec_1_neutral_loss_617_avge_mass "616.5636"
-xref: spec_1_neutral_loss_617_flag "false"
-xref: spec_1_neutral_loss_617_composition "dHex(2) Hex(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_617_mono_mass "616.221465"
-xref: spec_1_neutral_loss_617_avge_mass "616.5636"
-xref: spec_1_neutral_loss_617_flag "false"
-xref: spec_1_neutral_loss_617_composition "dHex(2) Hex(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1446
-name: dHex(1)Hex(2)HexA(1)
-def: "DHex Hex(2) HexA." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=2&hexa=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1446]
-xref: record_id "1446"
-xref: delta_mono_mass "646.195644"
-xref: delta_avge_mass "646.5465"
-xref: delta_composition "dHex Hex(2) HexA"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 11:06:47"
-xref: date_time_modified "2015-05-05 11:06:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_647_mono_mass "646.195644"
-xref: spec_1_neutral_loss_647_avge_mass "646.5465"
-xref: spec_1_neutral_loss_647_flag "false"
-xref: spec_1_neutral_loss_647_composition "dHex Hex(2) HexA"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_647_mono_mass "646.195644"
-xref: spec_1_neutral_loss_647_avge_mass "646.5465"
-xref: spec_1_neutral_loss_647_flag "false"
-xref: spec_1_neutral_loss_647_composition "dHex Hex(2) HexA"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1447
-name: Hex(1)HexNAc(2)Sulf(1)
-def: "Hex HexNAc(2) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1447]
-xref: record_id "1447"
-xref: delta_mono_mass "648.168383"
-xref: delta_avge_mass "648.5888"
-xref: delta_composition "O(3) S Hex HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 11:09:57"
-xref: date_time_modified "2015-05-06 12:09:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_649_mono_mass "648.168383"
-xref: spec_1_neutral_loss_649_avge_mass "648.5888"
-xref: spec_1_neutral_loss_649_flag "false"
-xref: spec_1_neutral_loss_649_composition "O(3) S Hex HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_649_mono_mass "648.168383"
-xref: spec_1_neutral_loss_649_avge_mass "648.5888"
-xref: spec_1_neutral_loss_649_flag "false"
-xref: spec_1_neutral_loss_649_composition "O(3) S Hex HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1448
-name: Hex(4)
-def: "Hex(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1448]
-xref: record_id "1448"
-xref: delta_mono_mass "648.211294"
-xref: delta_avge_mass "648.5624"
-xref: delta_composition "Hex(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 11:10:47"
-xref: date_time_modified "2015-05-05 11:10:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_649_mono_mass "648.211294"
-xref: spec_1_neutral_loss_649_avge_mass "648.5624"
-xref: spec_1_neutral_loss_649_flag "false"
-xref: spec_1_neutral_loss_649_composition "Hex(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_649_mono_mass "648.211294"
-xref: spec_1_neutral_loss_649_avge_mass "648.5624"
-xref: spec_1_neutral_loss_649_flag "false"
-xref: spec_1_neutral_loss_649_composition "Hex(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1449
-name: dHex(1)Hex(2)HexNAc(2)Pent(1)
-def: "DHex Hex(2) HexNAc(2) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=2&hexnac=2&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1449]
-xref: record_id "1449"
-xref: delta_mono_mass "1008.36456"
-xref: delta_avge_mass "1008.9221"
-xref: delta_composition "dHex(1) Hex(2) HexNAc(2) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1009_mono_mass "1008.36456"
-xref: spec_1_neutral_loss_1009_avge_mass "1008.9221"
-xref: spec_1_neutral_loss_1009_flag "false"
-xref: spec_1_neutral_loss_1009_composition "dHex(1) Hex(2) HexNAc(2) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1450
-name: Hex(2)HexNAc(2)NeuAc(1)
-def: "Hex(2) HexNAc(2) NeuAc ---OR--- dHex Hex HexNAc(2) NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=2&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1450]
-xref: record_id "1450"
-xref: delta_mono_mass "1021.359809"
-xref: delta_avge_mass "1021.9208"
-xref: delta_composition "Hex(2) HexNAc(2) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-17 11:53:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1022_mono_mass "1021.359809"
-xref: spec_1_neutral_loss_1022_avge_mass "1021.9208"
-xref: spec_1_neutral_loss_1022_flag "false"
-xref: spec_1_neutral_loss_1022_composition "Hex(2) HexNAc(2) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_1022_mono_mass "1021.359809"
-xref: spec_2_neutral_loss_1022_avge_mass "1021.9208"
-xref: spec_2_neutral_loss_1022_flag "false"
-xref: spec_2_neutral_loss_1022_composition "Hex(2) HexNAc(2) NeuAc"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_1022_mono_mass "1021.359809"
-xref: spec_2_neutral_loss_1022_avge_mass "1021.9208"
-xref: spec_2_neutral_loss_1022_flag "false"
-xref: spec_2_neutral_loss_1022_composition "Hex(2) HexNAc(2) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1451
-name: Hex(3)HexNAc(2)Pent(1)
-def: "Hex(3) HexNAc(2) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=2&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1451]
-xref: record_id "1451"
-xref: delta_mono_mass "1024.359475"
-xref: delta_avge_mass "1024.9215"
-xref: delta_composition "Hex(3) HexNAc(2) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1025_mono_mass "1024.359475"
-xref: spec_1_neutral_loss_1025_avge_mass "1024.9215"
-xref: spec_1_neutral_loss_1025_flag "false"
-xref: spec_1_neutral_loss_1025_composition "Hex(3) HexNAc(2) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1452
-name: Hex(4)HexNAc(2)
-def: "Hex(4) HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1452]
-xref: record_id "1452"
-xref: delta_mono_mass "1054.370039"
-xref: delta_avge_mass "1054.9474"
-xref: delta_composition "Hex(4) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1055_mono_mass "1054.370039"
-xref: spec_1_neutral_loss_1055_avge_mass "1054.9474"
-xref: spec_1_neutral_loss_1055_flag "false"
-xref: spec_1_neutral_loss_1055_composition "Hex(4) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1453
-name: dHex(1)Hex(4)HexNAc(1)Pent(1)
-def: "DHex Hex(4) HexNAc Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=4&hexnac=1&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1453]
-xref: record_id "1453"
-xref: delta_mono_mass "1129.390834"
-xref: delta_avge_mass "1130.0107"
-xref: delta_composition "dHex(1) Hex(4) HexNAc(1) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1130_mono_mass "1129.390834"
-xref: spec_1_neutral_loss_1130_avge_mass "1130.0107"
-xref: spec_1_neutral_loss_1130_flag "false"
-xref: spec_1_neutral_loss_1130_composition "dHex(1) Hex(4) HexNAc(1) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1454
-name: dHex(1)Hex(3)HexNAc(2)Pent(1)
-def: "DHex Hex(3) HexNAc(2) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexnac=2&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1454]
-xref: record_id "1454"
-xref: delta_mono_mass "1170.417383"
-xref: delta_avge_mass "1171.0627"
-xref: delta_composition "dHex(1) Hex(3) HexNAc(2) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1171_mono_mass "1170.417383"
-xref: spec_1_neutral_loss_1171_avge_mass "1171.0627"
-xref: spec_1_neutral_loss_1171_flag "false"
-xref: spec_1_neutral_loss_1171_composition "dHex(1) Hex(3) HexNAc(2) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1455
-name: Hex(3)HexNAc(2)NeuAc(1)
-def: "Hex(3) HexNAc(2) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=2&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1455]
-xref: record_id "1455"
-xref: delta_mono_mass "1183.412632"
-xref: delta_avge_mass "1184.0614"
-xref: delta_composition "Hex(3) HexNAc(2) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1184_mono_mass "1183.412632"
-xref: spec_1_neutral_loss_1184_avge_mass "1184.0614"
-xref: spec_1_neutral_loss_1184_flag "false"
-xref: spec_1_neutral_loss_1184_composition "Hex(3) HexNAc(2) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1456
-name: Hex(4)HexNAc(2)Pent(1)
-def: "Hex(4) HexNAc(2) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexnac=2&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1456]
-xref: record_id "1456"
-xref: delta_mono_mass "1186.412298"
-xref: delta_avge_mass "1187.0621"
-xref: delta_composition "Hex(4) HexNAc(2) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1187_mono_mass "1186.412298"
-xref: spec_1_neutral_loss_1187_avge_mass "1187.0621"
-xref: spec_1_neutral_loss_1187_flag "false"
-xref: spec_1_neutral_loss_1187_composition "Hex(4) HexNAc(2) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1457
-name: Hex(3)HexNAc(3)Pent(1)
-def: "Hex(3) HexNAc(3) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=3&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1457]
-xref: record_id "1457"
-xref: delta_mono_mass "1227.438847"
-xref: delta_avge_mass "1228.114"
-xref: delta_composition "Hex(3) HexNAc(3) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1228_mono_mass "1227.438847"
-xref: spec_1_neutral_loss_1228_avge_mass "1228.114"
-xref: spec_1_neutral_loss_1228_flag "false"
-xref: spec_1_neutral_loss_1228_composition "Hex(3) HexNAc(3) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1458
-name: Hex(5)HexNAc(2)Phos(1)
-def: "Hex(5) HexNAc(2) Phos." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=1&hex=5&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1458]
-xref: record_id "1458"
-xref: delta_mono_mass "1296.389194"
-xref: delta_avge_mass "1297.0679"
-xref: delta_composition "H O(3) P Hex(5) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:43:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1297_mono_mass "1296.389194"
-xref: spec_1_neutral_loss_1297_avge_mass "1297.0679"
-xref: spec_1_neutral_loss_1297_flag "false"
-xref: spec_1_neutral_loss_1297_composition "H O(3) P Hex(5) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1459
-name: dHex(1)Hex(4)HexNAc(2)Pent(1)
-def: "DHex Hex(4) HexNAc(2) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=4&hexnac=2&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1459]
-xref: record_id "1459"
-xref: delta_mono_mass "1332.470207"
-xref: delta_avge_mass "1333.2033"
-xref: delta_composition "dHex(1) Hex(4) HexNAc(2) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1333_mono_mass "1332.470207"
-xref: spec_1_neutral_loss_1333_avge_mass "1333.2033"
-xref: spec_1_neutral_loss_1333_flag "false"
-xref: spec_1_neutral_loss_1333_composition "dHex(1) Hex(4) HexNAc(2) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1460
-name: Hex(7)HexNAc(1)
-def: "Hex(7) HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=7&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1460]
-xref: record_id "1460"
-xref: delta_mono_mass "1337.449137"
-xref: delta_avge_mass "1338.1767"
-xref: delta_composition "Hex(7) HexNAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1338_mono_mass "1337.449137"
-xref: spec_1_neutral_loss_1338_avge_mass "1338.1767"
-xref: spec_1_neutral_loss_1338_flag "false"
-xref: spec_1_neutral_loss_1338_composition "Hex(7) HexNAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1461
-name: Hex(4)HexNAc(2)NeuAc(1)
-def: "Hex(4) HexNAc(2) NeuAc ---OR--- Hex(3) HexNAc(2) dHex NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexnac=2&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1461]
-xref: record_id "1461"
-xref: delta_mono_mass "1345.465456"
-xref: delta_avge_mass "1346.202"
-xref: delta_composition "Hex(4) HexNAc(2) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-17 13:30:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1346_mono_mass "1345.465456"
-xref: spec_1_neutral_loss_1346_avge_mass "1346.202"
-xref: spec_1_neutral_loss_1346_flag "false"
-xref: spec_1_neutral_loss_1346_composition "Hex(4) HexNAc(2) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_1346_mono_mass "1345.465456"
-xref: spec_2_neutral_loss_1346_avge_mass "1346.202"
-xref: spec_2_neutral_loss_1346_flag "false"
-xref: spec_2_neutral_loss_1346_composition "Hex(4) HexNAc(2) NeuAc"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_1346_mono_mass "1345.465456"
-xref: spec_2_neutral_loss_1346_avge_mass "1346.202"
-xref: spec_2_neutral_loss_1346_flag "false"
-xref: spec_2_neutral_loss_1346_composition "Hex(4) HexNAc(2) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1462
-name: dHex(1)Hex(5)HexNAc(2)
-def: "DHex Hex(5) HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=5&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1462]
-xref: record_id "1462"
-xref: delta_mono_mass "1362.480772"
-xref: delta_avge_mass "1363.2292"
-xref: delta_composition "dHex(1) Hex(5) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1363_mono_mass "1362.480772"
-xref: spec_1_neutral_loss_1363_avge_mass "1363.2292"
-xref: spec_1_neutral_loss_1363_flag "false"
-xref: spec_1_neutral_loss_1363_composition "dHex(1) Hex(5) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1463
-name: dHex(1)Hex(3)HexNAc(3)Pent(1)
-def: "DHex Hex(3) HexNAc(3) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexnac=3&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1463]
-xref: record_id "1463"
-xref: delta_mono_mass "1373.496756"
-xref: delta_avge_mass "1374.2552"
-xref: delta_composition "dHex(1) Hex(3) HexNAc(3) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1374_mono_mass "1373.496756"
-xref: spec_1_neutral_loss_1374_avge_mass "1374.2552"
-xref: spec_1_neutral_loss_1374_flag "false"
-xref: spec_1_neutral_loss_1374_composition "dHex(1) Hex(3) HexNAc(3) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1464
-name: Hex(3)HexNAc(4)Sulf(1)
-def: "Hex(3) HexNAc(4) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=3&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1464]
-xref: record_id "1464"
-xref: delta_mono_mass "1378.432776"
-xref: delta_avge_mass "1379.2551"
-xref: delta_composition "O(3) S Hex(3) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:33:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1379_mono_mass "1378.432776"
-xref: spec_1_neutral_loss_1379_avge_mass "1379.2551"
-xref: spec_1_neutral_loss_1379_flag "false"
-xref: spec_1_neutral_loss_1379_composition "O(3) S Hex(3) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1465
-name: Hex(6)HexNAc(2)
-def: "M6/Man6." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=6&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1465]
-xref: record_id "1465"
-xref: delta_mono_mass "1378.475686"
-xref: delta_avge_mass "1379.2286"
-xref: delta_composition "Hex(6) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2020-08-02 11:49:46"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1379_mono_mass "1378.475686"
-xref: spec_1_neutral_loss_1379_avge_mass "1379.2286"
-xref: spec_1_neutral_loss_1379_flag "false"
-xref: spec_1_neutral_loss_1379_composition "Hex(6) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1466
-name: Hex(4)HexNAc(3)Pent(1)
-def: "Hex(4) HexNAc(3) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexnac=3&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1466]
-xref: record_id "1466"
-xref: delta_mono_mass "1389.491671"
-xref: delta_avge_mass "1390.2546"
-xref: delta_composition "Hex(4) HexNAc(3) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1390_mono_mass "1389.491671"
-xref: spec_1_neutral_loss_1390_avge_mass "1390.2546"
-xref: spec_1_neutral_loss_1390_flag "false"
-xref: spec_1_neutral_loss_1390_composition "Hex(4) HexNAc(3) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1467
-name: dHex(1)Hex(4)HexNAc(3)
-def: "DHex Hex(4) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=4&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1467]
-xref: record_id "1467"
-xref: delta_mono_mass "1403.507321"
-xref: delta_avge_mass "1404.2812"
-xref: delta_composition "dHex(1) Hex(4) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1404_mono_mass "1403.507321"
-xref: spec_1_neutral_loss_1404_avge_mass "1404.2812"
-xref: spec_1_neutral_loss_1404_flag "false"
-xref: spec_1_neutral_loss_1404_composition "dHex(1) Hex(4) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1468
-name: Hex(5)HexNAc(3)
-def: "Hex(5) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=5&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1468]
-xref: record_id "1468"
-xref: delta_mono_mass "1419.502235"
-xref: delta_avge_mass "1420.2806"
-xref: delta_composition "Hex(5) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1420_mono_mass "1419.502235"
-xref: spec_1_neutral_loss_1420_avge_mass "1420.2806"
-xref: spec_1_neutral_loss_1420_flag "false"
-xref: spec_1_neutral_loss_1420_composition "Hex(5) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1469
-name: Hex(3)HexNAc(4)Pent(1)
-def: "Hex(3) HexNAc(4) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=4&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1469]
-xref: record_id "1469"
-xref: delta_mono_mass "1430.51822"
-xref: delta_avge_mass "1431.3065"
-xref: delta_composition "Hex(3) HexNAc(4) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1431_mono_mass "1430.51822"
-xref: spec_1_neutral_loss_1431_avge_mass "1431.3065"
-xref: spec_1_neutral_loss_1431_flag "false"
-xref: spec_1_neutral_loss_1431_composition "Hex(3) HexNAc(4) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1470
-name: Hex(6)HexNAc(2)Phos(1)
-def: "Hex(6) HexNAc(2) Phos." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=1&hex=6&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1470]
-xref: record_id "1470"
-xref: delta_mono_mass "1458.442017"
-xref: delta_avge_mass "1459.2085"
-xref: delta_composition "H O(3) P Hex(6) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:43:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1459_mono_mass "1458.442017"
-xref: spec_1_neutral_loss_1459_avge_mass "1459.2085"
-xref: spec_1_neutral_loss_1459_flag "false"
-xref: spec_1_neutral_loss_1459_composition "H O(3) P Hex(6) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1471
-name: dHex(1)Hex(4)HexNAc(3)Sulf(1)
-def: "DHex Hex(4) HexNAc(3) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=4&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1471]
-xref: record_id "1471"
-xref: delta_mono_mass "1483.464135"
-xref: delta_avge_mass "1484.3444"
-xref: delta_composition "O(3) S dHex Hex(4) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:34:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1484_mono_mass "1483.464135"
-xref: spec_1_neutral_loss_1484_avge_mass "1484.3444"
-xref: spec_1_neutral_loss_1484_flag "false"
-xref: spec_1_neutral_loss_1484_composition "O(3) S dHex Hex(4) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1472
-name: dHex(1)Hex(5)HexNAc(2)Pent(1)
-def: "DHex Hex(5) HexNAc(2) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=5&hexnac=2&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1472]
-xref: record_id "1472"
-xref: delta_mono_mass "1494.52303"
-xref: delta_avge_mass "1495.3439"
-xref: delta_composition "dHex(1) Hex(5) HexNAc(2) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1495_mono_mass "1494.52303"
-xref: spec_1_neutral_loss_1495_avge_mass "1495.3439"
-xref: spec_1_neutral_loss_1495_flag "false"
-xref: spec_1_neutral_loss_1495_composition "dHex(1) Hex(5) HexNAc(2) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1473
-name: Hex(8)HexNAc(1)
-def: "Hex(8) HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=8&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1473]
-xref: record_id "1473"
-xref: delta_mono_mass "1499.501961"
-xref: delta_avge_mass "1500.3173"
-xref: delta_composition "Hex(8) HexNAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1500_mono_mass "1499.501961"
-xref: spec_1_neutral_loss_1500_avge_mass "1500.3173"
-xref: spec_1_neutral_loss_1500_flag "false"
-xref: spec_1_neutral_loss_1500_composition "Hex(8) HexNAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1474
-name: dHex(1)Hex(3)HexNAc(3)Pent(2)
-def: "DHex Hex(3) HexNAc(3) Pent(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexnac=3&pent=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1474]
-xref: record_id "1474"
-xref: delta_mono_mass "1505.539015"
-xref: delta_avge_mass "1506.3698"
-xref: delta_composition "dHex(1) Hex(3) HexNAc(3) Pent(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1506_mono_mass "1505.539015"
-xref: spec_1_neutral_loss_1506_avge_mass "1506.3698"
-xref: spec_1_neutral_loss_1506_flag "false"
-xref: spec_1_neutral_loss_1506_composition "dHex(1) Hex(3) HexNAc(3) Pent(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1475
-name: dHex(2)Hex(3)HexNAc(3)Pent(1)
-def: "DHex(2) Hex(3) HexNAc(3) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=3&hexnac=3&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1475]
-xref: record_id "1475"
-xref: delta_mono_mass "1519.554665"
-xref: delta_avge_mass "1520.3964"
-xref: delta_composition "dHex(2) Hex(3) HexNAc(3) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1520_mono_mass "1519.554665"
-xref: spec_1_neutral_loss_1520_avge_mass "1520.3964"
-xref: spec_1_neutral_loss_1520_flag "false"
-xref: spec_1_neutral_loss_1520_composition "dHex(2) Hex(3) HexNAc(3) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1476
-name: dHex(1)Hex(3)HexNAc(4)Sulf(1)
-def: "DHex Hex(3) HexNAc(4) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=3&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1476]
-xref: record_id "1476"
-xref: delta_mono_mass "1524.490684"
-xref: delta_avge_mass "1525.3963"
-xref: delta_composition "O(3) S dHex Hex(3) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:34:38"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1525_mono_mass "1524.490684"
-xref: spec_1_neutral_loss_1525_avge_mass "1525.3963"
-xref: spec_1_neutral_loss_1525_flag "false"
-xref: spec_1_neutral_loss_1525_composition "O(3) S dHex Hex(3) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1477
-name: dHex(1)Hex(6)HexNAc(2)
-def: "DHex Hex(6) HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=6&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1477]
-xref: record_id "1477"
-xref: delta_mono_mass "1524.533595"
-xref: delta_avge_mass "1525.3698"
-xref: delta_composition "dHex(1) Hex(6) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1525_mono_mass "1524.533595"
-xref: spec_1_neutral_loss_1525_avge_mass "1525.3698"
-xref: spec_1_neutral_loss_1525_flag "false"
-xref: spec_1_neutral_loss_1525_composition "dHex(1) Hex(6) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1478
-name: dHex(1)Hex(4)HexNAc(3)Pent(1)
-def: "DHex Hex(4) HexNAc(3) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=4&hexnac=3&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1478]
-xref: record_id "1478"
-xref: delta_mono_mass "1535.549579"
-xref: delta_avge_mass "1536.3958"
-xref: delta_composition "dHex(1) Hex(4) HexNAc(3) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1536_mono_mass "1535.549579"
-xref: spec_1_neutral_loss_1536_avge_mass "1536.3958"
-xref: spec_1_neutral_loss_1536_flag "false"
-xref: spec_1_neutral_loss_1536_composition "dHex(1) Hex(4) HexNAc(3) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1479
-name: Hex(4)HexNAc(4)Sulf(1)
-def: "Hex(4) HexNAc(4) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=4&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1479]
-xref: record_id "1479"
-xref: delta_mono_mass "1540.485599"
-xref: delta_avge_mass "1541.3957"
-xref: delta_composition "O(3) S Hex(4) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:34:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1541_mono_mass "1540.485599"
-xref: spec_1_neutral_loss_1541_avge_mass "1541.3957"
-xref: spec_1_neutral_loss_1541_flag "false"
-xref: spec_1_neutral_loss_1541_composition "O(3) S Hex(4) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1480
-name: Hex(7)HexNAc(2)
-def: "M7/Man7." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=7&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1480]
-xref: record_id "1480"
-xref: delta_mono_mass "1540.52851"
-xref: delta_avge_mass "1541.3692"
-xref: delta_composition "Hex(7) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2020-08-02 11:49:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1541_mono_mass "1540.52851"
-xref: spec_1_neutral_loss_1541_avge_mass "1541.3692"
-xref: spec_1_neutral_loss_1541_flag "false"
-xref: spec_1_neutral_loss_1541_composition "Hex(7) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1481
-name: dHex(2)Hex(4)HexNAc(3)
-def: "DHex(2) Hex(4) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=4&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1481]
-xref: record_id "1481"
-xref: delta_mono_mass "1549.56523"
-xref: delta_avge_mass "1550.4224"
-xref: delta_composition "dHex(2) Hex(4) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1550_mono_mass "1549.56523"
-xref: spec_1_neutral_loss_1550_avge_mass "1550.4224"
-xref: spec_1_neutral_loss_1550_flag "false"
-xref: spec_1_neutral_loss_1550_composition "dHex(2) Hex(4) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1482
-name: Hex(5)HexNAc(3)Pent(1)
-def: "Hex(5) HexNAc(3) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=5&hexnac=3&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1482]
-xref: record_id "1482"
-xref: delta_mono_mass "1551.544494"
-xref: delta_avge_mass "1552.3952"
-xref: delta_composition "Hex(5) HexNAc(3) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1552_mono_mass "1551.544494"
-xref: spec_1_neutral_loss_1552_avge_mass "1552.3952"
-xref: spec_1_neutral_loss_1552_flag "false"
-xref: spec_1_neutral_loss_1552_composition "Hex(5) HexNAc(3) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1483
-name: Hex(4)HexNAc(3)NeuGc(1)
-def: "Hex(4) HexNAc(3) NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexnac=3&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1483]
-xref: record_id "1483"
-xref: delta_mono_mass "1564.539743"
-xref: delta_avge_mass "1565.3939"
-xref: delta_composition "Hex(4) HexNAc(3) NeuGc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1565_mono_mass "1564.539743"
-xref: spec_1_neutral_loss_1565_avge_mass "1565.3939"
-xref: spec_1_neutral_loss_1565_flag "false"
-xref: spec_1_neutral_loss_1565_composition "Hex(4) HexNAc(3) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1484
-name: dHex(1)Hex(5)HexNAc(3)
-def: "DHex Hex(5) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=5&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1484]
-xref: record_id "1484"
-xref: delta_mono_mass "1565.560144"
-xref: delta_avge_mass "1566.4218"
-xref: delta_composition "dHex(1) Hex(5) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1566_mono_mass "1565.560144"
-xref: spec_1_neutral_loss_1566_avge_mass "1566.4218"
-xref: spec_1_neutral_loss_1566_flag "false"
-xref: spec_1_neutral_loss_1566_composition "dHex(1) Hex(5) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1485
-name: dHex(1)Hex(3)HexNAc(4)Pent(1)
-def: "DHex Hex(3) HexNAc(4) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexnac=4&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1485]
-xref: record_id "1485"
-xref: delta_mono_mass "1576.576129"
-xref: delta_avge_mass "1577.4477"
-xref: delta_composition "dHex(1) Hex(3) HexNAc(4) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1577_mono_mass "1576.576129"
-xref: spec_1_neutral_loss_1577_avge_mass "1577.4477"
-xref: spec_1_neutral_loss_1577_flag "false"
-xref: spec_1_neutral_loss_1577_composition "dHex(1) Hex(3) HexNAc(4) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1486
-name: Hex(3)HexNAc(5)Sulf(1)
-def: "Hex(3) HexNAc(5) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=3&hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1486]
-xref: record_id "1486"
-xref: delta_mono_mass "1581.512148"
-xref: delta_avge_mass "1582.4476"
-xref: delta_composition "O(3) S Hex(3) HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:35:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1582_mono_mass "1581.512148"
-xref: spec_1_neutral_loss_1582_avge_mass "1582.4476"
-xref: spec_1_neutral_loss_1582_flag "false"
-xref: spec_1_neutral_loss_1582_composition "O(3) S Hex(3) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1487
-name: Hex(6)HexNAc(3)
-def: "Hex(6) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=6&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1487]
-xref: record_id "1487"
-xref: delta_mono_mass "1581.555059"
-xref: delta_avge_mass "1582.4212"
-xref: delta_composition "Hex(6) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1582_mono_mass "1581.555059"
-xref: spec_1_neutral_loss_1582_avge_mass "1582.4212"
-xref: spec_1_neutral_loss_1582_flag "false"
-xref: spec_1_neutral_loss_1582_composition "Hex(6) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1488
-name: Hex(3)HexNAc(4)NeuAc(1)
-def: "Hex(3) HexNAc(4) NeuAc ---OR--- Hex(2) HexNAc(4) dHex NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=4&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1488]
-xref: record_id "1488"
-xref: delta_mono_mass "1589.571378"
-xref: delta_avge_mass "1590.4465"
-xref: delta_composition "Hex(3) HexNAc(4) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-17 16:47:58"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1590_mono_mass "1589.571378"
-xref: spec_1_neutral_loss_1590_avge_mass "1590.4465"
-xref: spec_1_neutral_loss_1590_flag "false"
-xref: spec_1_neutral_loss_1590_composition "Hex(3) HexNAc(4) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1489
-name: Hex(4)HexNAc(4)Pent(1)
-def: "Hex(4) HexNAc(4) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexnac=4&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1489]
-xref: record_id "1489"
-xref: delta_mono_mass "1592.571043"
-xref: delta_avge_mass "1593.4471"
-xref: delta_composition "Hex(4) HexNAc(4) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1593_mono_mass "1592.571043"
-xref: spec_1_neutral_loss_1593_avge_mass "1593.4471"
-xref: spec_1_neutral_loss_1593_flag "false"
-xref: spec_1_neutral_loss_1593_composition "Hex(4) HexNAc(4) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1490
-name: Hex(7)HexNAc(2)Phos(1)
-def: "Hex(7) HexNAc(2) Phos." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=1&hex=7&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1490]
-xref: record_id "1490"
-xref: delta_mono_mass "1620.494841"
-xref: delta_avge_mass "1621.3491"
-xref: delta_composition "H O(3) P Hex(7) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:43:48"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1621_mono_mass "1620.494841"
-xref: spec_1_neutral_loss_1621_avge_mass "1621.3491"
-xref: spec_1_neutral_loss_1621_flag "false"
-xref: spec_1_neutral_loss_1621_composition "H O(3) P Hex(7) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1491
-name: Hex(4)HexNAc(4)Me(2)Pent(1)
-def: "Hex(4) HexNAc(4) Me(2) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexnac=4&methyl=2&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1491]
-xref: record_id "1491"
-xref: delta_mono_mass "1620.602343"
-xref: delta_avge_mass "1621.5003"
-xref: delta_composition "Hex(4) HexNAc(4) Me(2) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1621_mono_mass "1620.602343"
-xref: spec_1_neutral_loss_1621_avge_mass "1621.5003"
-xref: spec_1_neutral_loss_1621_flag "false"
-xref: spec_1_neutral_loss_1621_composition "Hex(4) HexNAc(4) Me(2) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1492
-name: dHex(1)Hex(3)HexNAc(3)Pent(3)
-def: "DHex Hex(3) HexNAc(3) Pent(3) ---OR--- Hex(4) HexNAc(2) dHex(2) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?pent=3&dhex=1&hex=3&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1492]
-xref: record_id "1492"
-xref: delta_mono_mass "1637.581274"
-xref: delta_avge_mass "1638.4844"
-xref: delta_composition "Pent(3) dHex Hex(3) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-22 10:46:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1638_mono_mass "1637.581274"
-xref: spec_1_neutral_loss_1638_avge_mass "1638.4844"
-xref: spec_1_neutral_loss_1638_flag "false"
-xref: spec_1_neutral_loss_1638_composition "Pent(3) dHex Hex(3) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1493
-name: dHex(1)Hex(5)HexNAc(3)Sulf(1)
-def: "DHex Hex(5) HexNAc(3) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=5&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1493]
-xref: record_id "1493"
-xref: delta_mono_mass "1645.516959"
-xref: delta_avge_mass "1646.485"
-xref: delta_composition "O(3) S dHex Hex(5) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:35:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1646_mono_mass "1645.516959"
-xref: spec_1_neutral_loss_1646_avge_mass "1646.485"
-xref: spec_1_neutral_loss_1646_flag "false"
-xref: spec_1_neutral_loss_1646_composition "O(3) S dHex Hex(5) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1494
-name: dHex(2)Hex(3)HexNAc(3)Pent(2)
-def: "DHex(2) Hex(3) HexNAc(3) Pent(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=3&hexnac=3&pent=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1494]
-xref: record_id "1494"
-xref: delta_mono_mass "1651.596924"
-xref: delta_avge_mass "1652.511"
-xref: delta_composition "dHex(2) Hex(3) HexNAc(3) Pent(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1652_mono_mass "1651.596924"
-xref: spec_1_neutral_loss_1652_avge_mass "1652.511"
-xref: spec_1_neutral_loss_1652_flag "false"
-xref: spec_1_neutral_loss_1652_composition "dHex(2) Hex(3) HexNAc(3) Pent(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1495
-name: Hex(6)HexNAc(3)Phos(1)
-def: "Hex(6) HexNAc(3) Phos." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=1&hex=6&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1495]
-xref: record_id "1495"
-xref: delta_mono_mass "1661.52139"
-xref: delta_avge_mass "1662.4011"
-xref: delta_composition "H O(3) P Hex(6) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:43:58"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1662_mono_mass "1661.52139"
-xref: spec_1_neutral_loss_1662_avge_mass "1662.4011"
-xref: spec_1_neutral_loss_1662_flag "false"
-xref: spec_1_neutral_loss_1662_composition "H O(3) P Hex(6) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1496
-name: Hex(4)HexNAc(5)
-def: "Hex(4) HexNAc(5)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1496]
-xref: record_id "1496"
-xref: delta_mono_mass "1663.608157"
-xref: delta_avge_mass "1664.525"
-xref: delta_composition "Hex(4) HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1664_mono_mass "1663.608157"
-xref: spec_1_neutral_loss_1664_avge_mass "1664.525"
-xref: spec_1_neutral_loss_1664_flag "false"
-xref: spec_1_neutral_loss_1664_composition "Hex(4) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1497
-name: dHex(3)Hex(3)HexNAc(3)Pent(1)
-def: "DHex(3) Hex(3) HexNAc(3) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=3&hex=3&hexnac=3&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1497]
-xref: record_id "1497"
-xref: delta_mono_mass "1665.612574"
-xref: delta_avge_mass "1666.5376"
-xref: delta_composition "dHex(3) Hex(3) HexNAc(3) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1666_mono_mass "1665.612574"
-xref: spec_1_neutral_loss_1666_avge_mass "1666.5376"
-xref: spec_1_neutral_loss_1666_flag "false"
-xref: spec_1_neutral_loss_1666_composition "dHex(3) Hex(3) HexNAc(3) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1498
-name: dHex(2)Hex(4)HexNAc(3)Pent(1)
-def: "DHex(2) Hex(4) HexNAc(3) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=4&hexnac=3&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1498]
-xref: record_id "1498"
-xref: delta_mono_mass "1681.607488"
-xref: delta_avge_mass "1682.537"
-xref: delta_composition "dHex(2) Hex(4) HexNAc(3) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1682_mono_mass "1681.607488"
-xref: spec_1_neutral_loss_1682_avge_mass "1682.537"
-xref: spec_1_neutral_loss_1682_flag "false"
-xref: spec_1_neutral_loss_1682_composition "dHex(2) Hex(4) HexNAc(3) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1499
-name: dHex(1)Hex(4)HexNAc(4)Sulf(1)
-def: "DHex Hex(4) HexNAc(4) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=4&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1499]
-xref: record_id "1499"
-xref: delta_mono_mass "1686.543508"
-xref: delta_avge_mass "1687.5369"
-xref: delta_composition "O(3) S dHex Hex(4) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:35:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1687_mono_mass "1686.543508"
-xref: spec_1_neutral_loss_1687_avge_mass "1687.5369"
-xref: spec_1_neutral_loss_1687_flag "false"
-xref: spec_1_neutral_loss_1687_composition "O(3) S dHex Hex(4) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1500
-name: dHex(1)Hex(7)HexNAc(2)
-def: "DHex Hex(7) HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=7&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1500]
-xref: record_id "1500"
-xref: delta_mono_mass "1686.586419"
-xref: delta_avge_mass "1687.5104"
-xref: delta_composition "dHex(1) Hex(7) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1687_mono_mass "1686.586419"
-xref: spec_1_neutral_loss_1687_avge_mass "1687.5104"
-xref: spec_1_neutral_loss_1687_flag "false"
-xref: spec_1_neutral_loss_1687_composition "dHex(1) Hex(7) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1501
-name: dHex(1)Hex(4)HexNAc(3)NeuAc(1)
-def: "DHex Hex(4) HexNAc(3) NeuAc ---OR--- dHex(2) Hex(3) HexNAc(3) NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=4&hexnac=3&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1501]
-xref: record_id "1501"
-xref: delta_mono_mass "1694.602737"
-xref: delta_avge_mass "1695.5357"
-xref: delta_composition "dHex Hex(4) HexNAc(3) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-22 10:54:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1695_mono_mass "1694.602737"
-xref: spec_1_neutral_loss_1695_avge_mass "1695.5357"
-xref: spec_1_neutral_loss_1695_flag "false"
-xref: spec_1_neutral_loss_1695_composition "dHex Hex(4) HexNAc(3) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_1695_mono_mass "1694.602737"
-xref: spec_2_neutral_loss_1695_avge_mass "1695.5357"
-xref: spec_2_neutral_loss_1695_flag "false"
-xref: spec_2_neutral_loss_1695_composition "dHex Hex(4) HexNAc(3) NeuAc"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_1695_mono_mass "1694.602737"
-xref: spec_2_neutral_loss_1695_avge_mass "1695.5357"
-xref: spec_2_neutral_loss_1695_flag "false"
-xref: spec_2_neutral_loss_1695_composition "dHex Hex(4) HexNAc(3) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1502
-name: Hex(7)HexNAc(2)Phos(2)
-def: "Hex(7) HexNAc(2) Phos(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=2&hex=7&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1502]
-xref: record_id "1502"
-xref: delta_mono_mass "1700.461172"
-xref: delta_avge_mass "1701.329"
-xref: delta_composition "H(2) O(6) P(2) Hex(7) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:44:09"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1701_mono_mass "1700.461172"
-xref: spec_1_neutral_loss_1701_avge_mass "1701.329"
-xref: spec_1_neutral_loss_1701_flag "false"
-xref: spec_1_neutral_loss_1701_composition "H(2) O(6) P(2) Hex(7) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1503
-name: Hex(5)HexNAc(4)Sulf(1)
-def: "Hex(5) HexNAc(4) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=5&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1503]
-xref: record_id "1503"
-xref: delta_mono_mass "1702.538423"
-xref: delta_avge_mass "1703.5363"
-xref: delta_composition "O(3) S Hex(5) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:35:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1703_mono_mass "1702.538423"
-xref: spec_1_neutral_loss_1703_avge_mass "1703.5363"
-xref: spec_1_neutral_loss_1703_flag "false"
-xref: spec_1_neutral_loss_1703_composition "O(3) S Hex(5) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1504
-name: Hex(8)HexNAc(2)
-def: "M8/Man8." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=8&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1504]
-xref: record_id "1504"
-xref: delta_mono_mass "1702.581333"
-xref: delta_avge_mass "1703.5098"
-xref: delta_composition "Hex(8) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2020-08-02 11:49:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1703_mono_mass "1702.581333"
-xref: spec_1_neutral_loss_1703_avge_mass "1703.5098"
-xref: spec_1_neutral_loss_1703_flag "false"
-xref: spec_1_neutral_loss_1703_composition "Hex(8) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1505
-name: dHex(1)Hex(3)HexNAc(4)Pent(2)
-def: "DHex Hex(3) HexNAc(4) Pent(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexnac=4&pent=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1505]
-xref: record_id "1505"
-xref: delta_mono_mass "1708.618387"
-xref: delta_avge_mass "1709.5623"
-xref: delta_composition "dHex(1) Hex(3) HexNAc(4) Pent(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1709_mono_mass "1708.618387"
-xref: spec_1_neutral_loss_1709_avge_mass "1709.5623"
-xref: spec_1_neutral_loss_1709_flag "false"
-xref: spec_1_neutral_loss_1709_composition "dHex(1) Hex(3) HexNAc(4) Pent(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1506
-name: dHex(1)Hex(4)HexNAc(3)NeuGc(1)
-def: "DHex Hex(4) HexNAc(3) NeuGc ---OR--- Hex(5) HexNAc(3) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=4&hexnac=3&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1506]
-xref: record_id "1506"
-xref: delta_mono_mass "1710.597652"
-xref: delta_avge_mass "1711.5351"
-xref: delta_composition "dHex Hex(4) HexNAc(3) NeuGc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-22 11:04:22"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1711_mono_mass "1710.597652"
-xref: spec_1_neutral_loss_1711_avge_mass "1711.5351"
-xref: spec_1_neutral_loss_1711_flag "false"
-xref: spec_1_neutral_loss_1711_composition "dHex Hex(4) HexNAc(3) NeuGc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1507
-name: dHex(2)Hex(3)HexNAc(4)Pent(1)
-def: "DHex(2) Hex(3) HexNAc(4) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=3&hexnac=4&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1507]
-xref: record_id "1507"
-xref: delta_mono_mass "1722.634037"
-xref: delta_avge_mass "1723.5889"
-xref: delta_composition "dHex(2) Hex(3) HexNAc(4) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1723_mono_mass "1722.634037"
-xref: spec_1_neutral_loss_1723_avge_mass "1723.5889"
-xref: spec_1_neutral_loss_1723_flag "false"
-xref: spec_1_neutral_loss_1723_composition "dHex(2) Hex(3) HexNAc(4) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1508
-name: dHex(1)Hex(3)HexNAc(5)Sulf(1)
-def: "DHex Hex(3) HexNAc(5) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=3&hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1508]
-xref: record_id "1508"
-xref: delta_mono_mass "1727.570057"
-xref: delta_avge_mass "1728.5888"
-xref: delta_composition "O(3) S dHex Hex(3) HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:36:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1728_mono_mass "1727.570057"
-xref: spec_1_neutral_loss_1728_avge_mass "1728.5888"
-xref: spec_1_neutral_loss_1728_flag "false"
-xref: spec_1_neutral_loss_1728_composition "O(3) S dHex Hex(3) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1509
-name: dHex(1)Hex(6)HexNAc(3)
-def: "DHex Hex(6) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=6&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1509]
-xref: record_id "1509"
-xref: delta_mono_mass "1727.612968"
-xref: delta_avge_mass "1728.5624"
-xref: delta_composition "dHex(1) Hex(6) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1728_mono_mass "1727.612968"
-xref: spec_1_neutral_loss_1728_avge_mass "1728.5624"
-xref: spec_1_neutral_loss_1728_flag "false"
-xref: spec_1_neutral_loss_1728_composition "dHex(1) Hex(6) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1510
-name: dHex(1)Hex(3)HexNAc(4)NeuAc(1)
-def: "DHex Hex(3) HexNAc(4) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexnac=4&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1510]
-xref: record_id "1510"
-xref: delta_mono_mass "1735.629286"
-xref: delta_avge_mass "1736.5877"
-xref: delta_composition "dHex(1) Hex(3) HexNAc(4) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1736_mono_mass "1735.629286"
-xref: spec_1_neutral_loss_1736_avge_mass "1736.5877"
-xref: spec_1_neutral_loss_1736_flag "false"
-xref: spec_1_neutral_loss_1736_composition "dHex(1) Hex(3) HexNAc(4) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1511
-name: dHex(3)Hex(3)HexNAc(4)
-def: "DHex(3) Hex(3) HexNAc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=3&hex=3&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1511]
-xref: record_id "1511"
-xref: delta_mono_mass "1736.649688"
-xref: delta_avge_mass "1737.6155"
-xref: delta_composition "dHex(3) Hex(3) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1737_mono_mass "1736.649688"
-xref: spec_1_neutral_loss_1737_avge_mass "1737.6155"
-xref: spec_1_neutral_loss_1737_flag "false"
-xref: spec_1_neutral_loss_1737_composition "dHex(3) Hex(3) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1512
-name: dHex(1)Hex(4)HexNAc(4)Pent(1)
-def: "DHex Hex(4) HexNAc(4) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=4&hexnac=4&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1512]
-xref: record_id "1512"
-xref: delta_mono_mass "1738.628952"
-xref: delta_avge_mass "1739.5883"
-xref: delta_composition "dHex(1) Hex(4) HexNAc(4) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1739_mono_mass "1738.628952"
-xref: spec_1_neutral_loss_1739_avge_mass "1739.5883"
-xref: spec_1_neutral_loss_1739_flag "false"
-xref: spec_1_neutral_loss_1739_composition "dHex(1) Hex(4) HexNAc(4) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1513
-name: Hex(4)HexNAc(5)Sulf(1)
-def: "Hex(4) HexNAc(5) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=4&hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1513]
-xref: record_id "1513"
-xref: delta_mono_mass "1743.564972"
-xref: delta_avge_mass "1744.5882"
-xref: delta_composition "O(3) S Hex(4) HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:36:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1744_mono_mass "1743.564972"
-xref: spec_1_neutral_loss_1744_avge_mass "1744.5882"
-xref: spec_1_neutral_loss_1744_flag "false"
-xref: spec_1_neutral_loss_1744_composition "O(3) S Hex(4) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1514
-name: Hex(7)HexNAc(3)
-def: "Hex(7) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=7&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1514]
-xref: record_id "1514"
-xref: delta_mono_mass "1743.607882"
-xref: delta_avge_mass "1744.5618"
-xref: delta_composition "Hex(7) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1744_mono_mass "1743.607882"
-xref: spec_1_neutral_loss_1744_avge_mass "1744.5618"
-xref: spec_1_neutral_loss_1744_flag "false"
-xref: spec_1_neutral_loss_1744_composition "Hex(7) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1515
-name: dHex(1)Hex(4)HexNAc(3)NeuAc(1)Sulf(1)
-def: "DHex Hex(4) HexNAc(3) NeuAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=4&hexnac=3&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1515]
-xref: record_id "1515"
-xref: delta_mono_mass "1774.559552"
-xref: delta_avge_mass "1775.5989"
-xref: delta_composition "O(3) S dHex Hex(4) HexNAc(3) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:36:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1775_mono_mass "1774.559552"
-xref: spec_1_neutral_loss_1775_avge_mass "1775.5989"
-xref: spec_1_neutral_loss_1775_flag "false"
-xref: spec_1_neutral_loss_1775_composition "O(3) S dHex Hex(4) HexNAc(3) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1516
-name: Hex(5)HexNAc(4)Me(2)Pent(1)
-def: "Hex(5) HexNAc(4) Me(2) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=5&hexnac=4&methyl=2&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1516]
-xref: record_id "1516"
-xref: delta_mono_mass "1782.655167"
-xref: delta_avge_mass "1783.6409"
-xref: delta_composition "Hex(5) HexNAc(4) Me(2) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1783_mono_mass "1782.655167"
-xref: spec_1_neutral_loss_1783_avge_mass "1783.6409"
-xref: spec_1_neutral_loss_1783_flag "false"
-xref: spec_1_neutral_loss_1783_composition "Hex(5) HexNAc(4) Me(2) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1517
-name: Hex(3)HexNAc(6)Sulf(1)
-def: "Hex(3) HexNAc(6) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=3&hexnac=6&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1517]
-xref: record_id "1517"
-xref: delta_mono_mass "1784.591521"
-xref: delta_avge_mass "1785.6401"
-xref: delta_composition "O(3) S Hex(3) HexNAc(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:36:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1785_mono_mass "1784.591521"
-xref: spec_1_neutral_loss_1785_avge_mass "1785.6401"
-xref: spec_1_neutral_loss_1785_flag "false"
-xref: spec_1_neutral_loss_1785_composition "O(3) S Hex(3) HexNAc(6)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1518
-name: dHex(1)Hex(6)HexNAc(3)Sulf(1)
-def: "DHex Hex(6) HexNAc(3) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=6&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1518]
-xref: record_id "1518"
-xref: delta_mono_mass "1807.569782"
-xref: delta_avge_mass "1808.6256"
-xref: delta_composition "O(3) S dHex Hex(6) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:36:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1808_mono_mass "1807.569782"
-xref: spec_1_neutral_loss_1808_avge_mass "1808.6256"
-xref: spec_1_neutral_loss_1808_flag "false"
-xref: spec_1_neutral_loss_1808_composition "O(3) S dHex Hex(6) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1519
-name: dHex(1)Hex(4)HexNAc(5)
-def: "DHex Hex(4) HexNAc(5)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=4&hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1519]
-xref: record_id "1519"
-xref: delta_mono_mass "1809.666066"
-xref: delta_avge_mass "1810.6662"
-xref: delta_composition "dHex(1) Hex(4) HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1810_mono_mass "1809.666066"
-xref: spec_1_neutral_loss_1810_avge_mass "1810.6662"
-xref: spec_1_neutral_loss_1810_flag "false"
-xref: spec_1_neutral_loss_1810_composition "dHex(1) Hex(4) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1520
-name: dHex(1)Hex(5)HexA(1)HexNAc(3)Sulf(1)
-def: "DHex Hex(5) HexA HexNAc(3) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=5&hexa=1&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1520]
-xref: record_id "1520"
-xref: delta_mono_mass "1821.549047"
-xref: delta_avge_mass "1822.6091"
-xref: delta_composition "O(3) S dHex Hex(5) HexA HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:37:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1822_mono_mass "1821.549047"
-xref: spec_1_neutral_loss_1822_avge_mass "1822.6091"
-xref: spec_1_neutral_loss_1822_flag "false"
-xref: spec_1_neutral_loss_1822_composition "O(3) S dHex Hex(5) HexA HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1521
-name: Hex(7)HexNAc(3)Phos(1)
-def: "Hex(7) HexNAc(3) Phos." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=1&hex=7&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1521]
-xref: record_id "1521"
-xref: delta_mono_mass "1823.574213"
-xref: delta_avge_mass "1824.5417"
-xref: delta_composition "H O(3) P Hex(7) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:44:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1824_mono_mass "1823.574213"
-xref: spec_1_neutral_loss_1824_avge_mass "1824.5417"
-xref: spec_1_neutral_loss_1824_flag "false"
-xref: spec_1_neutral_loss_1824_composition "H O(3) P Hex(7) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1522
-name: Hex(6)HexNAc(4)Me(3)
-def: "Hex(6) HexNAc(4) Me(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=6&hexnac=4&methyl=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1522]
-xref: record_id "1522"
-xref: delta_mono_mass "1826.681382"
-xref: delta_avge_mass "1827.6934"
-xref: delta_composition "Hex(6) HexNAc(4) Me(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1827_mono_mass "1826.681382"
-xref: spec_1_neutral_loss_1827_avge_mass "1827.6934"
-xref: spec_1_neutral_loss_1827_flag "false"
-xref: spec_1_neutral_loss_1827_composition "Hex(6) HexNAc(4) Me(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1523
-name: dHex(2)Hex(4)HexNAc(4)Sulf(1)
-def: "DHex(2) Hex(4) HexNAc(4) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=2&hex=4&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1523]
-xref: record_id "1523"
-xref: delta_mono_mass "1832.601417"
-xref: delta_avge_mass "1833.6781"
-xref: delta_composition "O(3) S dHex(2) Hex(4) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:37:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1833_mono_mass "1832.601417"
-xref: spec_1_neutral_loss_1833_avge_mass "1833.6781"
-xref: spec_1_neutral_loss_1833_flag "false"
-xref: spec_1_neutral_loss_1833_composition "O(3) S dHex(2) Hex(4) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1524
-name: Hex(4)HexNAc(3)NeuAc(2)
-def: "Hex(4) HexNAc(3) NeuAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexnac=3&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1524]
-xref: record_id "1524"
-xref: delta_mono_mass "1839.640245"
-xref: delta_avge_mass "1840.6491"
-xref: delta_composition "Hex(4) HexNAc(3) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1840_mono_mass "1839.640245"
-xref: spec_1_neutral_loss_1840_avge_mass "1840.6491"
-xref: spec_1_neutral_loss_1840_flag "false"
-xref: spec_1_neutral_loss_1840_composition "Hex(4) HexNAc(3) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1525
-name: dHex(1)Hex(3)HexNAc(4)Pent(3)
-def: "DHex Hex(3) HexNAc(4) Pent(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexnac=4&pent=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1525]
-xref: record_id "1525"
-xref: delta_mono_mass "1840.660646"
-xref: delta_avge_mass "1841.6769"
-xref: delta_composition "dHex(1) Hex(3) HexNAc(4) Pent(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1841_mono_mass "1840.660646"
-xref: spec_1_neutral_loss_1841_avge_mass "1841.6769"
-xref: spec_1_neutral_loss_1841_flag "false"
-xref: spec_1_neutral_loss_1841_composition "dHex(1) Hex(3) HexNAc(4) Pent(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1526
-name: dHex(2)Hex(5)HexNAc(3)Pent(1)
-def: "DHex(2) Hex(5) HexNAc(3) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=5&hexnac=3&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1526]
-xref: record_id "1526"
-xref: delta_mono_mass "1843.660312"
-xref: delta_avge_mass "1844.6776"
-xref: delta_composition "dHex(2) Hex(5) HexNAc(3) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1844_mono_mass "1843.660312"
-xref: spec_1_neutral_loss_1844_avge_mass "1844.6776"
-xref: spec_1_neutral_loss_1844_flag "false"
-xref: spec_1_neutral_loss_1844_composition "dHex(2) Hex(5) HexNAc(3) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1527
-name: dHex(1)Hex(5)HexNAc(4)Sulf(1)
-def: "DHex Hex(5) HexNAc(4) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=5&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1527]
-xref: record_id "1527"
-xref: delta_mono_mass "1848.596331"
-xref: delta_avge_mass "1849.6775"
-xref: delta_composition "O(3) S dHex Hex(5) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:37:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1849_mono_mass "1848.596331"
-xref: spec_1_neutral_loss_1849_avge_mass "1849.6775"
-xref: spec_1_neutral_loss_1849_flag "false"
-xref: spec_1_neutral_loss_1849_composition "O(3) S dHex Hex(5) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1528
-name: dHex(2)Hex(3)HexNAc(4)Pent(2)
-def: "DHex(2) Hex(3) HexNAc(4) Pent(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=3&hexnac=4&pent=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1528]
-xref: record_id "1528"
-xref: delta_mono_mass "1854.676296"
-xref: delta_avge_mass "1855.7035"
-xref: delta_composition "dHex(2) Hex(3) HexNAc(4) Pent(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1855_mono_mass "1854.676296"
-xref: spec_1_neutral_loss_1855_avge_mass "1855.7035"
-xref: spec_1_neutral_loss_1855_flag "false"
-xref: spec_1_neutral_loss_1855_composition "dHex(2) Hex(3) HexNAc(4) Pent(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1529
-name: dHex(1)Hex(5)HexNAc(3)NeuAc(1)
-def: "DHex Hex(5) HexNAc(3) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=5&hexnac=3&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1529]
-xref: record_id "1529"
-xref: delta_mono_mass "1856.655561"
-xref: delta_avge_mass "1857.6763"
-xref: delta_composition "dHex(1) Hex(5) HexNAc(3) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1857_mono_mass "1856.655561"
-xref: spec_1_neutral_loss_1857_avge_mass "1857.6763"
-xref: spec_1_neutral_loss_1857_flag "false"
-xref: spec_1_neutral_loss_1857_composition "dHex(1) Hex(5) HexNAc(3) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1530
-name: Hex(3)HexNAc(6)Sulf(2)
-def: "Hex(3) HexNAc(6) Sulf(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=2&hex=3&hexnac=6&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1530]
-xref: record_id "1530"
-xref: delta_mono_mass "1864.548335"
-xref: delta_avge_mass "1865.7033"
-xref: delta_composition "O(6) S(2) Hex(3) HexNAc(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:37:39"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1865_mono_mass "1864.548335"
-xref: spec_1_neutral_loss_1865_avge_mass "1865.7033"
-xref: spec_1_neutral_loss_1865_flag "false"
-xref: spec_1_neutral_loss_1865_composition "O(6) S(2) Hex(3) HexNAc(6)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1531
-name: Hex(9)HexNAc(2)
-def: "M9/Man9." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=9&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1531]
-xref: record_id "1531"
-xref: delta_mono_mass "1864.634157"
-xref: delta_avge_mass "1865.6504"
-xref: delta_composition "Hex(9) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2020-08-02 11:48:38"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1865_mono_mass "1864.634157"
-xref: spec_1_neutral_loss_1865_avge_mass "1865.6504"
-xref: spec_1_neutral_loss_1865_flag "false"
-xref: spec_1_neutral_loss_1865_composition "Hex(9) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1532
-name: Hex(4)HexNAc(6)
-def: "Hex(4) HexNAc(6)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexnac=6&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1532]
-xref: record_id "1532"
-xref: delta_mono_mass "1866.68753"
-xref: delta_avge_mass "1867.7175"
-xref: delta_composition "Hex(4) HexNAc(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1867_mono_mass "1866.68753"
-xref: spec_1_neutral_loss_1867_avge_mass "1867.7175"
-xref: spec_1_neutral_loss_1867_flag "false"
-xref: spec_1_neutral_loss_1867_composition "Hex(4) HexNAc(6)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1533
-name: dHex(3)Hex(3)HexNAc(4)Pent(1)
-def: "DHex(3) Hex(3) HexNAc(4) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=3&hex=3&hexnac=4&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1533]
-xref: record_id "1533"
-xref: delta_mono_mass "1868.691946"
-xref: delta_avge_mass "1869.7301"
-xref: delta_composition "dHex(3) Hex(3) HexNAc(4) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1869_mono_mass "1868.691946"
-xref: spec_1_neutral_loss_1869_avge_mass "1869.7301"
-xref: spec_1_neutral_loss_1869_flag "false"
-xref: spec_1_neutral_loss_1869_composition "dHex(3) Hex(3) HexNAc(4) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1534
-name: dHex(1)Hex(5)HexNAc(3)NeuGc(1)
-def: "DHex Hex(5) HexNAc(3) NeuGc ---OR--- Hex(6) HexNAc(3) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=5&hexnac=3&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1534]
-xref: record_id "1534"
-xref: delta_mono_mass "1872.650475"
-xref: delta_avge_mass "1873.6757"
-xref: delta_composition "dHex Hex(5) HexNAc(3) NeuGc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-22 11:15:38"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1873_mono_mass "1872.650475"
-xref: spec_1_neutral_loss_1873_avge_mass "1873.6757"
-xref: spec_1_neutral_loss_1873_flag "false"
-xref: spec_1_neutral_loss_1873_composition "dHex Hex(5) HexNAc(3) NeuGc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1535
-name: dHex(2)Hex(4)HexNAc(4)Pent(1)
-def: "DHex(2) Hex(4) HexNAc(4) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=4&hexnac=4&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1535]
-xref: record_id "1535"
-xref: delta_mono_mass "1884.686861"
-xref: delta_avge_mass "1885.7295"
-xref: delta_composition "dHex(2) Hex(4) HexNAc(4) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1885_mono_mass "1884.686861"
-xref: spec_1_neutral_loss_1885_avge_mass "1885.7295"
-xref: spec_1_neutral_loss_1885_flag "false"
-xref: spec_1_neutral_loss_1885_composition "dHex(2) Hex(4) HexNAc(4) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1536
-name: dHex(1)Hex(4)HexNAc(5)Sulf(1)
-def: "DHex Hex(4) HexNAc(5) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=4&hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1536]
-xref: record_id "1536"
-xref: delta_mono_mass "1889.62288"
-xref: delta_avge_mass "1890.7294"
-xref: delta_composition "O(3) S dHex Hex(4) HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:37:53"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1890_mono_mass "1889.62288"
-xref: spec_1_neutral_loss_1890_avge_mass "1890.7294"
-xref: spec_1_neutral_loss_1890_flag "false"
-xref: spec_1_neutral_loss_1890_composition "O(3) S dHex Hex(4) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1537
-name: dHex(1)Hex(7)HexNAc(3)
-def: "DHex Hex(7) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=7&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1537]
-xref: record_id "1537"
-xref: delta_mono_mass "1889.665791"
-xref: delta_avge_mass "1890.703"
-xref: delta_composition "dHex(1) Hex(7) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1890_mono_mass "1889.665791"
-xref: spec_1_neutral_loss_1890_avge_mass "1890.703"
-xref: spec_1_neutral_loss_1890_flag "false"
-xref: spec_1_neutral_loss_1890_composition "dHex(1) Hex(7) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1538
-name: dHex(1)Hex(5)HexNAc(4)Pent(1)
-def: "DHex Hex(5) HexNAc(4) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=5&hexnac=4&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1538]
-xref: record_id "1538"
-xref: delta_mono_mass "1900.681776"
-xref: delta_avge_mass "1901.7289"
-xref: delta_composition "dHex(1) Hex(5) HexNAc(4) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1901_mono_mass "1900.681776"
-xref: spec_1_neutral_loss_1901_avge_mass "1901.7289"
-xref: spec_1_neutral_loss_1901_flag "false"
-xref: spec_1_neutral_loss_1901_composition "dHex(1) Hex(5) HexNAc(4) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1539
-name: dHex(1)Hex(5)HexA(1)HexNAc(3)Sulf(2)
-def: "DHex Hex(5) HexA HexNAc(3) Sulf(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=2&dhex=1&hex=5&hexa=1&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1539]
-xref: record_id "1539"
-xref: delta_mono_mass "1901.505861"
-xref: delta_avge_mass "1902.6723"
-xref: delta_composition "O(6) S(2) dHex Hex(5) HexA HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:38:08"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1902_mono_mass "1901.505861"
-xref: spec_1_neutral_loss_1902_avge_mass "1902.6723"
-xref: spec_1_neutral_loss_1902_flag "false"
-xref: spec_1_neutral_loss_1902_composition "O(6) S(2) dHex Hex(5) HexA HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1540
-name: Hex(3)HexNAc(7)
-def: "Hex(3) HexNAc(7)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=7&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1540]
-xref: record_id "1540"
-xref: delta_mono_mass "1907.714079"
-xref: delta_avge_mass "1908.7694"
-xref: delta_composition "Hex(3) HexNAc(7)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1908_mono_mass "1907.714079"
-xref: spec_1_neutral_loss_1908_avge_mass "1908.7694"
-xref: spec_1_neutral_loss_1908_flag "false"
-xref: spec_1_neutral_loss_1908_composition "Hex(3) HexNAc(7)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1541
-name: dHex(2)Hex(5)HexNAc(4)
-def: "DHex(2) Hex(5) HexNAc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=5&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1541]
-xref: record_id "1541"
-xref: delta_mono_mass "1914.697426"
-xref: delta_avge_mass "1915.7555"
-xref: delta_composition "dHex(2) Hex(5) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1915_mono_mass "1914.697426"
-xref: spec_1_neutral_loss_1915_avge_mass "1915.7555"
-xref: spec_1_neutral_loss_1915_flag "false"
-xref: spec_1_neutral_loss_1915_composition "dHex(2) Hex(5) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1542
-name: dHex(2)Hex(4)HexNAc(3)NeuAc(1)Sulf(1)
-def: "DHex(2) Hex(4) HexNAc(3) NeuAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=2&hex=4&hexnac=3&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1542]
-xref: record_id "1542"
-xref: delta_mono_mass "1920.617461"
-xref: delta_avge_mass "1921.7401"
-xref: delta_composition "O(3) S dHex(2) Hex(4) HexNAc(3) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:38:20"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1921_mono_mass "1920.617461"
-xref: spec_1_neutral_loss_1921_avge_mass "1921.7401"
-xref: spec_1_neutral_loss_1921_flag "false"
-xref: spec_1_neutral_loss_1921_composition "O(3) S dHex(2) Hex(4) HexNAc(3) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1543
-name: dHex(1)Hex(5)HexNAc(4)Sulf(2)
-def: "DHex Hex(5) HexNAc(4) Sulf(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=2&dhex=1&hex=5&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1543]
-xref: record_id "1543"
-xref: delta_mono_mass "1928.553146"
-xref: delta_avge_mass "1929.7407"
-xref: delta_composition "O(6) S(2) dHex Hex(5) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:39:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1929_mono_mass "1928.553146"
-xref: spec_1_neutral_loss_1929_avge_mass "1929.7407"
-xref: spec_1_neutral_loss_1929_flag "false"
-xref: spec_1_neutral_loss_1929_composition "O(6) S(2) dHex Hex(5) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1544
-name: dHex(1)Hex(5)HexNAc(4)Me(2)Pent(1)
-def: "DHex Hex(5) HexNAc(4) Me(2) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=5&hexnac=4&methyl=2&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1544]
-xref: record_id "1544"
-xref: delta_mono_mass "1928.713076"
-xref: delta_avge_mass "1929.7821"
-xref: delta_composition "dHex(1) Hex(5) HexNAc(4) Me(2) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1929_mono_mass "1928.713076"
-xref: spec_1_neutral_loss_1929_avge_mass "1929.7821"
-xref: spec_1_neutral_loss_1929_flag "false"
-xref: spec_1_neutral_loss_1929_composition "dHex(1) Hex(5) HexNAc(4) Me(2) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1545
-name: Hex(5)HexNAc(4)NeuGc(1)
-def: "Hex(5) HexNAc(4) NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=5&hexnac=4&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1545]
-xref: record_id "1545"
-xref: delta_mono_mass "1929.671939"
-xref: delta_avge_mass "1930.7271"
-xref: delta_composition "Hex(5) HexNAc(4) NeuGc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1930_mono_mass "1929.671939"
-xref: spec_1_neutral_loss_1930_avge_mass "1930.7271"
-xref: spec_1_neutral_loss_1930_flag "false"
-xref: spec_1_neutral_loss_1930_composition "Hex(5) HexNAc(4) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1546
-name: dHex(1)Hex(3)HexNAc(6)Sulf(1)
-def: "DHex Hex(3) HexNAc(6) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=3&hexnac=6&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1546]
-xref: record_id "1546"
-xref: delta_mono_mass "1930.64943"
-xref: delta_avge_mass "1931.7813"
-xref: delta_composition "O(3) S dHex Hex(3) HexNAc(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:39:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1931_mono_mass "1930.64943"
-xref: spec_1_neutral_loss_1931_avge_mass "1931.7813"
-xref: spec_1_neutral_loss_1931_flag "false"
-xref: spec_1_neutral_loss_1931_composition "O(3) S dHex Hex(3) HexNAc(6)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1547
-name: dHex(1)Hex(6)HexNAc(4)
-def: "DHex Hex(6) HexNAc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=6&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1547]
-xref: record_id "1547"
-xref: delta_mono_mass "1930.69234"
-xref: delta_avge_mass "1931.7549"
-xref: delta_composition "dHex(1) Hex(6) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1931_mono_mass "1930.69234"
-xref: spec_1_neutral_loss_1931_avge_mass "1931.7549"
-xref: spec_1_neutral_loss_1931_flag "false"
-xref: spec_1_neutral_loss_1931_composition "dHex(1) Hex(6) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1548
-name: dHex(1)Hex(5)HexNAc(3)NeuAc(1)Sulf(1)
-def: "DHex Hex(5) HexNAc(3) NeuAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=5&hexnac=3&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1548]
-xref: record_id "1548"
-xref: delta_mono_mass "1936.612375"
-xref: delta_avge_mass "1937.7395"
-xref: delta_composition "O(3) S dHex Hex(5) HexNAc(3) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:39:43"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1937_mono_mass "1936.612375"
-xref: spec_1_neutral_loss_1937_avge_mass "1937.7395"
-xref: spec_1_neutral_loss_1937_flag "false"
-xref: spec_1_neutral_loss_1937_composition "O(3) S dHex Hex(5) HexNAc(3) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1549
-name: Hex(7)HexNAc(4)
-def: "Hex(7) HexNAc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=7&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1549]
-xref: record_id "1549"
-xref: delta_mono_mass "1946.687255"
-xref: delta_avge_mass "1947.7543"
-xref: delta_composition "Hex(7) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1947_mono_mass "1946.687255"
-xref: spec_1_neutral_loss_1947_avge_mass "1947.7543"
-xref: spec_1_neutral_loss_1947_flag "false"
-xref: spec_1_neutral_loss_1947_composition "Hex(7) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1550
-name: dHex(1)Hex(5)HexNAc(3)NeuGc(1)Sulf(1)
-def: "DHex Hex(5) HexNAc(3) NeuGc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=5&hexnac=3&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1550]
-xref: record_id "1550"
-xref: delta_mono_mass "1952.60729"
-xref: delta_avge_mass "1953.7389"
-xref: delta_composition "O(3) S dHex Hex(5) HexNAc(3) NeuGc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:39:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1953_mono_mass "1952.60729"
-xref: spec_1_neutral_loss_1953_avge_mass "1953.7389"
-xref: spec_1_neutral_loss_1953_flag "false"
-xref: spec_1_neutral_loss_1953_composition "O(3) S dHex Hex(5) HexNAc(3) NeuGc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1551
-name: Hex(4)HexNAc(5)NeuAc(1)
-def: "Hex(4) HexNAc(5) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexnac=5&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1551]
-xref: record_id "1551"
-xref: delta_mono_mass "1954.703574"
-xref: delta_avge_mass "1955.7796"
-xref: delta_composition "Hex(4) HexNAc(5) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1955_mono_mass "1954.703574"
-xref: spec_1_neutral_loss_1955_avge_mass "1955.7796"
-xref: spec_1_neutral_loss_1955_flag "false"
-xref: spec_1_neutral_loss_1955_composition "Hex(4) HexNAc(5) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1552
-name: Hex(6)HexNAc(4)Me(3)Pent(1)
-def: "Hex(6) HexNAc(4) Me(3) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=6&hexnac=4&methyl=3&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1552]
-xref: record_id "1552"
-xref: delta_mono_mass "1958.72364"
-xref: delta_avge_mass "1959.808"
-xref: delta_composition "Hex(6) HexNAc(4) Me(3) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1959_mono_mass "1958.72364"
-xref: spec_1_neutral_loss_1959_avge_mass "1959.808"
-xref: spec_1_neutral_loss_1959_flag "false"
-xref: spec_1_neutral_loss_1959_composition "Hex(6) HexNAc(4) Me(3) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1553
-name: dHex(1)Hex(7)HexNAc(3)Sulf(1)
-def: "DHex Hex(7) HexNAc(3) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=7&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1553]
-xref: record_id "1553"
-xref: delta_mono_mass "1969.622606"
-xref: delta_avge_mass "1970.7662"
-xref: delta_composition "O(3) S dHex Hex(7) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:40:07"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1970_mono_mass "1969.622606"
-xref: spec_1_neutral_loss_1970_avge_mass "1970.7662"
-xref: spec_1_neutral_loss_1970_flag "false"
-xref: spec_1_neutral_loss_1970_composition "O(3) S dHex Hex(7) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1554
-name: dHex(1)Hex(7)HexNAc(3)Phos(1)
-def: "DHex Hex(7) HexNAc(3) Phos." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=1&dhex=1&hex=7&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1554]
-xref: record_id "1554"
-xref: delta_mono_mass "1969.632122"
-xref: delta_avge_mass "1970.6829"
-xref: delta_composition "H O(3) P dHex Hex(7) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:44:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1970_mono_mass "1969.632122"
-xref: spec_1_neutral_loss_1970_avge_mass "1970.6829"
-xref: spec_1_neutral_loss_1970_flag "false"
-xref: spec_1_neutral_loss_1970_composition "H O(3) P dHex Hex(7) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1555
-name: dHex(1)Hex(5)HexNAc(5)
-def: "DHex Hex(5) HexNAc(5)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=5&hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1555]
-xref: record_id "1555"
-xref: delta_mono_mass "1971.718889"
-xref: delta_avge_mass "1972.8068"
-xref: delta_composition "dHex(1) Hex(5) HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1972_mono_mass "1971.718889"
-xref: spec_1_neutral_loss_1972_avge_mass "1972.8068"
-xref: spec_1_neutral_loss_1972_flag "false"
-xref: spec_1_neutral_loss_1972_composition "dHex(1) Hex(5) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1556
-name: dHex(1)Hex(4)HexNAc(4)NeuAc(1)Sulf(1)
-def: "DHex Hex(4) HexNAc(4) NeuAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=4&hexnac=4&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1556]
-xref: record_id "1556"
-xref: delta_mono_mass "1977.638925"
-xref: delta_avge_mass "1978.7915"
-xref: delta_composition "O(3) S dHex Hex(4) HexNAc(4) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:40:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1978_mono_mass "1977.638925"
-xref: spec_1_neutral_loss_1978_avge_mass "1978.7915"
-xref: spec_1_neutral_loss_1978_flag "false"
-xref: spec_1_neutral_loss_1978_composition "O(3) S dHex Hex(4) HexNAc(4) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1557
-name: dHex(3)Hex(4)HexNAc(4)Sulf(1)
-def: "DHex(3) Hex(4) HexNAc(4) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=3&hex=4&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1557]
-xref: record_id "1557"
-xref: delta_mono_mass "1978.659326"
-xref: delta_avge_mass "1979.8193"
-xref: delta_composition "O(3) S dHex(3) Hex(4) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:40:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1979_mono_mass "1978.659326"
-xref: spec_1_neutral_loss_1979_avge_mass "1979.8193"
-xref: spec_1_neutral_loss_1979_flag "false"
-xref: spec_1_neutral_loss_1979_composition "O(3) S dHex(3) Hex(4) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1558
-name: Hex(3)HexNAc(7)Sulf(1)
-def: "Hex(3) HexNAc(7) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=3&hexnac=7&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1558]
-xref: record_id "1558"
-xref: delta_mono_mass "1987.670893"
-xref: delta_avge_mass "1988.8326"
-xref: delta_composition "O(3) S Hex(3) HexNAc(7)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:40:39"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1988_mono_mass "1987.670893"
-xref: spec_1_neutral_loss_1988_avge_mass "1988.8326"
-xref: spec_1_neutral_loss_1988_flag "false"
-xref: spec_1_neutral_loss_1988_composition "O(3) S Hex(3) HexNAc(7)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1559
-name: Hex(6)HexNAc(5)
-def: "A3G3." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=6&hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1559]
-xref: record_id "1559"
-xref: delta_mono_mass "1987.713804"
-xref: delta_avge_mass "1988.8062"
-xref: delta_composition "Hex(6) HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2020-08-02 11:45:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1988_mono_mass "1987.713804"
-xref: spec_1_neutral_loss_1988_avge_mass "1988.8062"
-xref: spec_1_neutral_loss_1988_flag "false"
-xref: spec_1_neutral_loss_1988_composition "Hex(6) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1560
-name: Hex(5)HexNAc(4)NeuAc(1)Sulf(1)
-def: "Hex(5) HexNAc(4) NeuAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=5&hexnac=4&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1560]
-xref: record_id "1560"
-xref: delta_mono_mass "1993.633839"
-xref: delta_avge_mass "1994.7909"
-xref: delta_composition "O(3) S Hex(5) HexNAc(4) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:40:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1994_mono_mass "1993.633839"
-xref: spec_1_neutral_loss_1994_avge_mass "1994.7909"
-xref: spec_1_neutral_loss_1994_flag "false"
-xref: spec_1_neutral_loss_1994_composition "O(3) S Hex(5) HexNAc(4) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1561
-name: Hex(3)HexNAc(6)NeuAc(1)
-def: "Hex(3) HexNAc(6) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=6&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1561]
-xref: record_id "1561"
-xref: delta_mono_mass "1995.730123"
-xref: delta_avge_mass "1996.8315"
-xref: delta_composition "Hex(3) HexNAc(6) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1996_mono_mass "1995.730123"
-xref: spec_1_neutral_loss_1996_avge_mass "1996.8315"
-xref: spec_1_neutral_loss_1996_flag "false"
-xref: spec_1_neutral_loss_1996_composition "Hex(3) HexNAc(6) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1562
-name: dHex(2)Hex(3)HexNAc(6)
-def: "DHex(2) Hex(3) HexNAc(6)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=3&hexnac=6&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1562]
-xref: record_id "1562"
-xref: delta_mono_mass "1996.750524"
-xref: delta_avge_mass "1997.8593"
-xref: delta_composition "dHex(2) Hex(3) HexNAc(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1997_mono_mass "1996.750524"
-xref: spec_1_neutral_loss_1997_avge_mass "1997.8593"
-xref: spec_1_neutral_loss_1997_flag "false"
-xref: spec_1_neutral_loss_1997_composition "dHex(2) Hex(3) HexNAc(6)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1563
-name: Hex(1)HexNAc(1)NeuGc(1)
-def: "Hex HexNAc NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=1&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1563]
-xref: record_id "1563"
-xref: delta_mono_mass "672.222527"
-xref: delta_avge_mass "672.5871"
-xref: delta_composition "Hex(1) HexNAc(1) NeuGc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_673_mono_mass "672.222527"
-xref: spec_1_neutral_loss_673_avge_mass "672.5871"
-xref: spec_1_neutral_loss_673_flag "false"
-xref: spec_1_neutral_loss_673_composition "Hex(1) HexNAc(1) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_673_mono_mass "672.222527"
-xref: spec_1_neutral_loss_673_avge_mass "672.5871"
-xref: spec_1_neutral_loss_673_flag "false"
-xref: spec_1_neutral_loss_673_composition "Hex(1) HexNAc(1) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1564
-name: dHex(1)Hex(2)HexNAc(1)
-def: "DHex Hex(2) HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=2&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1564]
-xref: record_id "1564"
-xref: delta_mono_mass "673.242928"
-xref: delta_avge_mass "673.6149"
-xref: delta_composition "dHex(1) Hex(2) HexNAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_674_mono_mass "673.242928"
-xref: spec_1_neutral_loss_674_avge_mass "673.6149"
-xref: spec_1_neutral_loss_674_flag "false"
-xref: spec_1_neutral_loss_674_composition "dHex(1) Hex(2) HexNAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_674_mono_mass "673.242928"
-xref: spec_1_neutral_loss_674_avge_mass "673.6149"
-xref: spec_1_neutral_loss_674_flag "false"
-xref: spec_1_neutral_loss_674_composition "dHex(1) Hex(2) HexNAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1565
-name: HexNAc(3)Sulf(1)
-def: "HexNAc(3) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1565]
-xref: record_id "1565"
-xref: delta_mono_mass "689.194932"
-xref: delta_avge_mass "689.6408"
-xref: delta_composition "O(3) S HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:26:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_690_mono_mass "689.194932"
-xref: spec_1_neutral_loss_690_avge_mass "689.6408"
-xref: spec_1_neutral_loss_690_flag "false"
-xref: spec_1_neutral_loss_690_composition "O(3) S HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_690_mono_mass "689.194932"
-xref: spec_1_neutral_loss_690_avge_mass "689.6408"
-xref: spec_1_neutral_loss_690_flag "false"
-xref: spec_1_neutral_loss_690_composition "O(3) S HexNAc(3)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1566
-name: Hex(3)HexNAc(1)
-def: "Hex(3) HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1566]
-xref: record_id "1566"
-xref: delta_mono_mass "689.237843"
-xref: delta_avge_mass "689.6143"
-xref: delta_composition "Hex(3) HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-23 17:47:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_690_mono_mass "689.237843"
-xref: spec_1_neutral_loss_690_avge_mass "689.6143"
-xref: spec_1_neutral_loss_690_flag "false"
-xref: spec_1_neutral_loss_690_composition "Hex(3) HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_690_mono_mass "689.237843"
-xref: spec_1_neutral_loss_690_avge_mass "689.6143"
-xref: spec_1_neutral_loss_690_flag "false"
-xref: spec_1_neutral_loss_690_composition "Hex(3) HexNAc"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_690_mono_mass "689.237843"
-xref: spec_2_neutral_loss_690_avge_mass "689.6143"
-xref: spec_2_neutral_loss_690_flag "false"
-xref: spec_2_neutral_loss_690_composition "Hex(3) HexNAc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1567
-name: Hex(1)HexNAc(1)Kdn(1)Sulf(1)
-def: "Hex HexNAc Kdn Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=1&hexnac=1&kdn=1)mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1567]
-xref: record_id "1567"
-xref: delta_mono_mass "695.157878"
-xref: delta_avge_mass "695.599"
-xref: delta_composition "O(3) S Hex HexNAc Kdn"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:26:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_696_mono_mass "695.157878"
-xref: spec_1_neutral_loss_696_avge_mass "695.599"
-xref: spec_1_neutral_loss_696_flag "false"
-xref: spec_1_neutral_loss_696_composition "O(3) S Hex HexNAc Kdn"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_696_mono_mass "695.157878"
-xref: spec_1_neutral_loss_696_avge_mass "695.599"
-xref: spec_1_neutral_loss_696_flag "false"
-xref: spec_1_neutral_loss_696_composition "O(3) S Hex HexNAc Kdn"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1568
-name: HexNAc(2)NeuAc(1)
-def: "HexNAc(2) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hexnac=2&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1568]
-xref: record_id "1568"
-xref: delta_mono_mass "697.254162"
-xref: delta_avge_mass "697.6396"
-xref: delta_composition "HexNAc(2) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_698_mono_mass "697.254162"
-xref: spec_1_neutral_loss_698_avge_mass "697.6396"
-xref: spec_1_neutral_loss_698_flag "false"
-xref: spec_1_neutral_loss_698_composition "HexNAc(2) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_698_mono_mass "697.254162"
-xref: spec_1_neutral_loss_698_avge_mass "697.6396"
-xref: spec_1_neutral_loss_698_flag "false"
-xref: spec_1_neutral_loss_698_composition "HexNAc(2) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1570
-name: HexNAc(1)Kdn(2)
-def: "HexNAc Kdn(2) ---OR--- Hex(2) HexNAc HexA." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hexnac=1&kdn=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1570]
-xref: record_id "1570"
-xref: delta_mono_mass "703.217108"
-xref: delta_avge_mass "703.5978"
-xref: delta_composition "HexNAc Kdn(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-17 11:43:15"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_704_mono_mass "703.217108"
-xref: spec_1_neutral_loss_704_avge_mass "703.5978"
-xref: spec_1_neutral_loss_704_flag "false"
-xref: spec_1_neutral_loss_704_composition "HexNAc Kdn(2)"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_704_mono_mass "703.217108"
-xref: spec_1_neutral_loss_704_avge_mass "703.5978"
-xref: spec_1_neutral_loss_704_flag "false"
-xref: spec_1_neutral_loss_704_composition "HexNAc Kdn(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1571
-name: Hex(3)HexNAc(1)Me(1)
-def: "Hex(3) HexNAc Me." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=1&methyl=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1571]
-xref: record_id "1571"
-xref: delta_mono_mass "703.253493"
-xref: delta_avge_mass "703.6409"
-xref: delta_composition "Hex(3) HexNAc(1) Me(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_704_mono_mass "703.253493"
-xref: spec_1_neutral_loss_704_avge_mass "703.6409"
-xref: spec_1_neutral_loss_704_flag "false"
-xref: spec_1_neutral_loss_704_composition "Hex(3) HexNAc(1) Me(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_704_mono_mass "703.253493"
-xref: spec_1_neutral_loss_704_avge_mass "703.6409"
-xref: spec_1_neutral_loss_704_flag "false"
-xref: spec_1_neutral_loss_704_composition "Hex(3) HexNAc(1) Me(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1572
-name: Hex(2)HexA(1)Pent(1)Sulf(1)
-def: "Hex(2) HexA Pent Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&pent=1&hex=2&hexa=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1572]
-xref: record_id "1572"
-xref: delta_mono_mass "712.136808"
-xref: delta_avge_mass "712.5831"
-xref: delta_composition "O(3) S Pent Hex(2) HexA"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:27:09"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_713_mono_mass "712.136808"
-xref: spec_1_neutral_loss_713_avge_mass "712.5831"
-xref: spec_1_neutral_loss_713_flag "false"
-xref: spec_1_neutral_loss_713_composition "O(3) S Pent Hex(2) HexA"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_713_mono_mass "712.136808"
-xref: spec_1_neutral_loss_713_avge_mass "712.5831"
-xref: spec_1_neutral_loss_713_flag "false"
-xref: spec_1_neutral_loss_713_composition "O(3) S Pent Hex(2) HexA"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1573
-name: HexNAc(2)NeuGc(1)
-def: "HexNAc(2) NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hexnac=2&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1573]
-xref: record_id "1573"
-xref: delta_mono_mass "713.249076"
-xref: delta_avge_mass "713.639"
-xref: delta_composition "HexNAc(2) NeuGc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_714_mono_mass "713.249076"
-xref: spec_1_neutral_loss_714_avge_mass "713.639"
-xref: spec_1_neutral_loss_714_flag "false"
-xref: spec_1_neutral_loss_714_composition "HexNAc(2) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_714_mono_mass "713.249076"
-xref: spec_1_neutral_loss_714_avge_mass "713.639"
-xref: spec_1_neutral_loss_714_flag "false"
-xref: spec_1_neutral_loss_714_composition "HexNAc(2) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1575
-name: Hex(4)Phos(1)
-def: "Hex(4) Phos." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=1&hex=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1575]
-xref: record_id "1575"
-xref: delta_mono_mass "728.177625"
-xref: delta_avge_mass "728.5423"
-xref: delta_composition "H O(3) P Hex(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:42:07"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_729_mono_mass "728.177625"
-xref: spec_1_neutral_loss_729_avge_mass "728.5423"
-xref: spec_1_neutral_loss_729_flag "false"
-xref: spec_1_neutral_loss_729_composition "H O(3) P Hex(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_729_mono_mass "728.177625"
-xref: spec_1_neutral_loss_729_avge_mass "728.5423"
-xref: spec_1_neutral_loss_729_flag "false"
-xref: spec_1_neutral_loss_729_composition "H O(3) P Hex(4)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1577
-name: Hex(1)HexNAc(1)NeuAc(1)Sulf(1)
-def: "Hex HexNAc NeuAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=1&hexnac=1&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1577]
-xref: record_id "1577"
-xref: delta_mono_mass "736.184427"
-xref: delta_avge_mass "736.6509"
-xref: delta_composition "O(3) S Hex HexNAc NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:27:24"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_737_mono_mass "736.184427"
-xref: spec_1_neutral_loss_737_avge_mass "736.6509"
-xref: spec_1_neutral_loss_737_flag "false"
-xref: spec_1_neutral_loss_737_composition "O(3) S Hex HexNAc NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_737_mono_mass "736.184427"
-xref: spec_1_neutral_loss_737_avge_mass "736.6509"
-xref: spec_1_neutral_loss_737_flag "false"
-xref: spec_1_neutral_loss_737_composition "O(3) S Hex HexNAc NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1578
-name: Hex(1)HexA(1)HexNAc(2)
-def: "Hex HexA HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexa=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1578]
-xref: record_id "1578"
-xref: delta_mono_mass "744.243657"
-xref: delta_avge_mass "744.6498"
-xref: delta_composition "Hex(1) HexA(1) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_745_mono_mass "744.243657"
-xref: spec_1_neutral_loss_745_avge_mass "744.6498"
-xref: spec_1_neutral_loss_745_flag "false"
-xref: spec_1_neutral_loss_745_composition "Hex(1) HexA(1) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_745_mono_mass "744.243657"
-xref: spec_1_neutral_loss_745_avge_mass "744.6498"
-xref: spec_1_neutral_loss_745_flag "false"
-xref: spec_1_neutral_loss_745_composition "Hex(1) HexA(1) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1579
-name: dHex(1)Hex(2)HexNAc(1)Sulf(1)
-def: "DHex Hex(2) HexNAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=2&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1579]
-xref: record_id "1579"
-xref: delta_mono_mass "753.199743"
-xref: delta_avge_mass "753.6781"
-xref: delta_composition "O(3) S dHex Hex(2) HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:27:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_754_mono_mass "753.199743"
-xref: spec_1_neutral_loss_754_avge_mass "753.6781"
-xref: spec_1_neutral_loss_754_flag "false"
-xref: spec_1_neutral_loss_754_composition "O(3) S dHex Hex(2) HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_754_mono_mass "753.199743"
-xref: spec_1_neutral_loss_754_avge_mass "753.6781"
-xref: spec_1_neutral_loss_754_flag "false"
-xref: spec_1_neutral_loss_754_composition "O(3) S dHex Hex(2) HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1580
-name: dHex(1)HexNAc(3)
-def: "DHex HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1580]
-xref: record_id "1580"
-xref: delta_mono_mass "755.296027"
-xref: delta_avge_mass "755.7188"
-xref: delta_composition "dHex(1) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_756_mono_mass "755.296027"
-xref: spec_1_neutral_loss_756_avge_mass "755.7188"
-xref: spec_1_neutral_loss_756_flag "false"
-xref: spec_1_neutral_loss_756_composition "dHex(1) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_756_mono_mass "755.296027"
-xref: spec_1_neutral_loss_756_avge_mass "755.7188"
-xref: spec_1_neutral_loss_756_flag "false"
-xref: spec_1_neutral_loss_756_composition "dHex(1) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1581
-name: dHex(1)Hex(1)HexNAc(1)Kdn(1)
-def: "DHex Hex HexNAc Kdn ---OR--- Hex(2) dHex NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=1&hexnac=1&kdn=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1581]
-xref: record_id "1581"
-xref: delta_mono_mass "761.258973"
-xref: delta_avge_mass "761.677"
-xref: delta_composition "dHex Hex HexNAc Kdn"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-17 11:43:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_762_mono_mass "761.258973"
-xref: spec_1_neutral_loss_762_avge_mass "761.677"
-xref: spec_1_neutral_loss_762_flag "false"
-xref: spec_1_neutral_loss_762_composition "dHex Hex HexNAc Kdn"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_762_mono_mass "761.258973"
-xref: spec_1_neutral_loss_762_avge_mass "761.677"
-xref: spec_1_neutral_loss_762_flag "false"
-xref: spec_1_neutral_loss_762_composition "dHex Hex HexNAc Kdn"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1582
-name: Hex(1)HexNAc(3)
-def: "Hex HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1582]
-xref: record_id "1582"
-xref: delta_mono_mass "771.290941"
-xref: delta_avge_mass "771.7182"
-xref: delta_composition "Hex(1) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_772_mono_mass "771.290941"
-xref: spec_1_neutral_loss_772_avge_mass "771.7182"
-xref: spec_1_neutral_loss_772_flag "false"
-xref: spec_1_neutral_loss_772_composition "Hex(1) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_772_mono_mass "771.290941"
-xref: spec_1_neutral_loss_772_avge_mass "771.7182"
-xref: spec_1_neutral_loss_772_flag "false"
-xref: spec_1_neutral_loss_772_composition "Hex(1) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1583
-name: HexNAc(2)NeuAc(1)Sulf(1)
-def: "HexNAc(2) NeuAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hexnac=2&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1583]
-xref: record_id "1583"
-xref: delta_mono_mass "777.210976"
-xref: delta_avge_mass "777.7028"
-xref: delta_composition "O(3) S HexNAc(2) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:27:46"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_778_mono_mass "777.210976"
-xref: spec_1_neutral_loss_778_avge_mass "777.7028"
-xref: spec_1_neutral_loss_778_flag "false"
-xref: spec_1_neutral_loss_778_composition "O(3) S HexNAc(2) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_778_mono_mass "777.210976"
-xref: spec_1_neutral_loss_778_avge_mass "777.7028"
-xref: spec_1_neutral_loss_778_flag "false"
-xref: spec_1_neutral_loss_778_composition "O(3) S HexNAc(2) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1584
-name: dHex(2)Hex(3)
-def: "DHex(2) Hex(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1584]
-xref: record_id "1584"
-xref: delta_mono_mass "778.274288"
-xref: delta_avge_mass "778.7042"
-xref: delta_composition "dHex(2) Hex(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_779_mono_mass "778.274288"
-xref: spec_1_neutral_loss_779_avge_mass "778.7042"
-xref: spec_1_neutral_loss_779_flag "false"
-xref: spec_1_neutral_loss_779_composition "dHex(2) Hex(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_779_mono_mass "778.274288"
-xref: spec_1_neutral_loss_779_avge_mass "778.7042"
-xref: spec_1_neutral_loss_779_flag "false"
-xref: spec_1_neutral_loss_779_composition "dHex(2) Hex(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1585
-name: Hex(2)HexA(1)HexNAc(1)Sulf(1)
-def: "Hex(2) HexA HexNAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=2&hexa=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1585]
-xref: record_id "1585"
-xref: delta_mono_mass "783.173922"
-xref: delta_avge_mass "783.661"
-xref: delta_composition "O(3) S Hex(2) HexA HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:28:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_784_mono_mass "783.173922"
-xref: spec_1_neutral_loss_784_avge_mass "783.661"
-xref: spec_1_neutral_loss_784_flag "false"
-xref: spec_1_neutral_loss_784_composition "O(3) S Hex(2) HexA HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_784_mono_mass "783.173922"
-xref: spec_1_neutral_loss_784_avge_mass "783.661"
-xref: spec_1_neutral_loss_784_flag "false"
-xref: spec_1_neutral_loss_784_composition "O(3) S Hex(2) HexA HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1586
-name: dHex(2)Hex(2)HexA(1)
-def: "DHex(2) Hex(2) HexA." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=2&hexa=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1586]
-xref: record_id "1586"
-xref: delta_mono_mass "792.253553"
-xref: delta_avge_mass "792.6877"
-xref: delta_composition "dHex(2) Hex(2) HexA(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_793_mono_mass "792.253553"
-xref: spec_1_neutral_loss_793_avge_mass "792.6877"
-xref: spec_1_neutral_loss_793_flag "false"
-xref: spec_1_neutral_loss_793_composition "dHex(2) Hex(2) HexA(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_793_mono_mass "792.253553"
-xref: spec_1_neutral_loss_793_avge_mass "792.6877"
-xref: spec_1_neutral_loss_793_flag "false"
-xref: spec_1_neutral_loss_793_composition "dHex(2) Hex(2) HexA(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1587
-name: dHex(1)Hex(1)HexNAc(2)Sulf(1)
-def: "DHex Hex HexNAc(2) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1587]
-xref: record_id "1587"
-xref: delta_mono_mass "794.226292"
-xref: delta_avge_mass "794.73"
-xref: delta_composition "O(3) S dHex Hex HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:28:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_795_mono_mass "794.226292"
-xref: spec_1_neutral_loss_795_avge_mass "794.73"
-xref: spec_1_neutral_loss_795_flag "false"
-xref: spec_1_neutral_loss_795_composition "O(3) S dHex Hex HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_795_mono_mass "794.226292"
-xref: spec_1_neutral_loss_795_avge_mass "794.73"
-xref: spec_1_neutral_loss_795_flag "false"
-xref: spec_1_neutral_loss_795_composition "O(3) S dHex Hex HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1588
-name: dHex(1)Hex(1)HexNAc(1)NeuAc(1)
-def: "DHex Hex HexNAc NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=1&hexnac=1&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1588]
-xref: record_id "1588"
-xref: delta_mono_mass "802.285522"
-xref: delta_avge_mass "802.7289"
-xref: delta_composition "dHex(1) Hex(1) HexNAc(1) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_803_mono_mass "802.285522"
-xref: spec_1_neutral_loss_803_avge_mass "802.7289"
-xref: spec_1_neutral_loss_803_flag "false"
-xref: spec_1_neutral_loss_803_composition "dHex(1) Hex(1) HexNAc(1) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_803_mono_mass "802.285522"
-xref: spec_1_neutral_loss_803_avge_mass "802.7289"
-xref: spec_1_neutral_loss_803_flag "false"
-xref: spec_1_neutral_loss_803_composition "dHex(1) Hex(1) HexNAc(1) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1589
-name: Hex(2)HexNAc(2)Sulf(1)
-def: "Hex(2) HexNAc(2) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=2&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1589]
-xref: record_id "1589"
-xref: delta_mono_mass "810.221207"
-xref: delta_avge_mass "810.7294"
-xref: delta_composition "O(3) S Hex(2) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:28:21"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_811_mono_mass "810.221207"
-xref: spec_1_neutral_loss_811_avge_mass "810.7294"
-xref: spec_1_neutral_loss_811_flag "false"
-xref: spec_1_neutral_loss_811_composition "O(3) S Hex(2) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_811_mono_mass "810.221207"
-xref: spec_1_neutral_loss_811_avge_mass "810.7294"
-xref: spec_1_neutral_loss_811_flag "false"
-xref: spec_1_neutral_loss_811_composition "O(3) S Hex(2) HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1590
-name: Hex(5)
-def: "Hex(5)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1590]
-xref: record_id "1590"
-xref: delta_mono_mass "810.264117"
-xref: delta_avge_mass "810.703"
-xref: delta_composition "Hex(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_811_mono_mass "810.264117"
-xref: spec_1_neutral_loss_811_avge_mass "810.703"
-xref: spec_1_neutral_loss_811_flag "false"
-xref: spec_1_neutral_loss_811_composition "Hex(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_811_mono_mass "810.264117"
-xref: spec_1_neutral_loss_811_avge_mass "810.703"
-xref: spec_1_neutral_loss_811_flag "false"
-xref: spec_1_neutral_loss_811_composition "Hex(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1591
-name: HexNAc(4)
-def: "HexNAc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1591]
-xref: record_id "1591"
-xref: delta_mono_mass "812.31749"
-xref: delta_avge_mass "812.7701"
-xref: delta_composition "HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_813_mono_mass "812.31749"
-xref: spec_1_neutral_loss_813_avge_mass "812.7701"
-xref: spec_1_neutral_loss_813_flag "false"
-xref: spec_1_neutral_loss_813_composition "HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_813_mono_mass "812.31749"
-xref: spec_1_neutral_loss_813_avge_mass "812.7701"
-xref: spec_1_neutral_loss_813_flag "false"
-xref: spec_1_neutral_loss_813_composition "HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1592
-name: HexNAc(1)NeuGc(2)
-def: "HexNAc NeuGc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hexnac=1&neugc=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1592]
-xref: record_id "1592"
-xref: delta_mono_mass "817.260035"
-xref: delta_avge_mass "817.7005"
-xref: delta_composition "HexNAc(1) NeuGc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_818_mono_mass "817.260035"
-xref: spec_1_neutral_loss_818_avge_mass "817.7005"
-xref: spec_1_neutral_loss_818_flag "false"
-xref: spec_1_neutral_loss_818_composition "HexNAc(1) NeuGc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_818_mono_mass "817.260035"
-xref: spec_1_neutral_loss_818_avge_mass "817.7005"
-xref: spec_1_neutral_loss_818_flag "false"
-xref: spec_1_neutral_loss_818_composition "HexNAc(1) NeuGc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1593
-name: dHex(1)Hex(1)HexNAc(1)NeuGc(1)
-def: "DHex Hex HexNAc NeuGc ---OR--- Hex(2) HexNAc NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=1&hexnac=1&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1593]
-xref: record_id "1593"
-xref: delta_mono_mass "818.280436"
-xref: delta_avge_mass "818.7283"
-xref: delta_composition "dHex Hex HexNAc NeuGc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-17 11:43:38"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_819_mono_mass "818.280436"
-xref: spec_1_neutral_loss_819_avge_mass "818.7283"
-xref: spec_1_neutral_loss_819_flag "false"
-xref: spec_1_neutral_loss_819_composition "dHex Hex HexNAc NeuGc"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_819_mono_mass "818.280436"
-xref: spec_1_neutral_loss_819_avge_mass "818.7283"
-xref: spec_1_neutral_loss_819_flag "false"
-xref: spec_1_neutral_loss_819_composition "dHex Hex HexNAc NeuGc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1594
-name: dHex(2)Hex(2)HexNAc(1)
-def: "DHex(2) Hex(2) HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=2&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1594]
-xref: record_id "1594"
-xref: delta_mono_mass "819.300837"
-xref: delta_avge_mass "819.7561"
-xref: delta_composition "dHex(2) Hex(2) HexNAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_820_mono_mass "819.300837"
-xref: spec_1_neutral_loss_820_avge_mass "819.7561"
-xref: spec_1_neutral_loss_820_flag "false"
-xref: spec_1_neutral_loss_820_composition "dHex(2) Hex(2) HexNAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_820_mono_mass "819.300837"
-xref: spec_1_neutral_loss_820_avge_mass "819.7561"
-xref: spec_1_neutral_loss_820_flag "false"
-xref: spec_1_neutral_loss_820_composition "dHex(2) Hex(2) HexNAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1595
-name: Hex(2)HexNAc(1)NeuGc(1)
-def: "Hex(2) HexNAc NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=1&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1595]
-xref: record_id "1595"
-xref: delta_mono_mass "834.275351"
-xref: delta_avge_mass "834.7277"
-xref: delta_composition "Hex(2) HexNAc(1) NeuGc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_835_mono_mass "834.275351"
-xref: spec_1_neutral_loss_835_avge_mass "834.7277"
-xref: spec_1_neutral_loss_835_flag "false"
-xref: spec_1_neutral_loss_835_composition "Hex(2) HexNAc(1) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_835_mono_mass "834.275351"
-xref: spec_1_neutral_loss_835_avge_mass "834.7277"
-xref: spec_1_neutral_loss_835_flag "false"
-xref: spec_1_neutral_loss_835_composition "Hex(2) HexNAc(1) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1596
-name: dHex(1)Hex(3)HexNAc(1)
-def: "DHex Hex(3) HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1596]
-xref: record_id "1596"
-xref: delta_mono_mass "835.295752"
-xref: delta_avge_mass "835.7555"
-xref: delta_composition "dHex(1) Hex(3) HexNAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_836_mono_mass "835.295752"
-xref: spec_1_neutral_loss_836_avge_mass "835.7555"
-xref: spec_1_neutral_loss_836_flag "false"
-xref: spec_1_neutral_loss_836_composition "dHex(1) Hex(3) HexNAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_836_mono_mass "835.295752"
-xref: spec_1_neutral_loss_836_avge_mass "835.7555"
-xref: spec_1_neutral_loss_836_flag "false"
-xref: spec_1_neutral_loss_836_composition "dHex(1) Hex(3) HexNAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1597
-name: dHex(1)Hex(2)HexA(1)HexNAc(1)
-def: "DHex Hex(2) HexA HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=2&hexa=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1597]
-xref: record_id "1597"
-xref: delta_mono_mass "849.275017"
-xref: delta_avge_mass "849.739"
-xref: delta_composition "dHex(1) Hex(2) HexA(1) HexNAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_850_mono_mass "849.275017"
-xref: spec_1_neutral_loss_850_avge_mass "849.739"
-xref: spec_1_neutral_loss_850_flag "false"
-xref: spec_1_neutral_loss_850_composition "dHex(1) Hex(2) HexA(1) HexNAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_850_mono_mass "849.275017"
-xref: spec_1_neutral_loss_850_avge_mass "849.739"
-xref: spec_1_neutral_loss_850_flag "false"
-xref: spec_1_neutral_loss_850_composition "dHex(1) Hex(2) HexA(1) HexNAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1598
-name: Hex(1)HexNAc(3)Sulf(1)
-def: "Hex HexNAc(3) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=1&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1598]
-xref: record_id "1598"
-xref: delta_mono_mass "851.247756"
-xref: delta_avge_mass "851.7814"
-xref: delta_composition "O(3) S Hex HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:28:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_852_mono_mass "851.247756"
-xref: spec_1_neutral_loss_852_avge_mass "851.7814"
-xref: spec_1_neutral_loss_852_flag "false"
-xref: spec_1_neutral_loss_852_composition "O(3) S Hex HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_852_mono_mass "851.247756"
-xref: spec_1_neutral_loss_852_avge_mass "851.7814"
-xref: spec_1_neutral_loss_852_flag "false"
-xref: spec_1_neutral_loss_852_composition "O(3) S Hex HexNAc(3)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1599
-name: Hex(4)HexNAc(1)
-def: "Hex(4) HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1599]
-xref: record_id "1599"
-xref: delta_mono_mass "851.290667"
-xref: delta_avge_mass "851.7549"
-xref: delta_composition "Hex(4) HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-24 10:39:59"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_852_mono_mass "851.290667"
-xref: spec_1_neutral_loss_852_avge_mass "851.7549"
-xref: spec_1_neutral_loss_852_flag "false"
-xref: spec_1_neutral_loss_852_composition "Hex(4) HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_852_mono_mass "851.290667"
-xref: spec_1_neutral_loss_852_avge_mass "851.7549"
-xref: spec_1_neutral_loss_852_flag "false"
-xref: spec_1_neutral_loss_852_composition "Hex(4) HexNAc"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_852_mono_mass "851.290667"
-xref: spec_2_neutral_loss_852_avge_mass "851.7549"
-xref: spec_2_neutral_loss_852_flag "false"
-xref: spec_2_neutral_loss_852_composition "Hex(4) HexNAc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1600
-name: Hex(1)HexNAc(2)NeuAc(1)
-def: "Hex HexNAc(2) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=2&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1600]
-xref: record_id "1600"
-xref: delta_mono_mass "859.306985"
-xref: delta_avge_mass "859.7802"
-xref: delta_composition "Hex(1) HexNAc(2) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_860_mono_mass "859.306985"
-xref: spec_1_neutral_loss_860_avge_mass "859.7802"
-xref: spec_1_neutral_loss_860_flag "false"
-xref: spec_1_neutral_loss_860_composition "Hex(1) HexNAc(2) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_860_mono_mass "859.306985"
-xref: spec_1_neutral_loss_860_avge_mass "859.7802"
-xref: spec_1_neutral_loss_860_flag "false"
-xref: spec_1_neutral_loss_860_composition "Hex(1) HexNAc(2) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1602
-name: Hex(1)HexNAc(2)NeuGc(1)
-def: "Hex HexNAc(2) NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=2&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1602]
-xref: record_id "1602"
-xref: delta_mono_mass "875.3019"
-xref: delta_avge_mass "875.7796"
-xref: delta_composition "Hex(1) HexNAc(2) NeuGc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_876_mono_mass "875.3019"
-xref: spec_1_neutral_loss_876_avge_mass "875.7796"
-xref: spec_1_neutral_loss_876_flag "false"
-xref: spec_1_neutral_loss_876_composition "Hex(1) HexNAc(2) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_876_mono_mass "875.3019"
-xref: spec_1_neutral_loss_876_avge_mass "875.7796"
-xref: spec_1_neutral_loss_876_flag "false"
-xref: spec_1_neutral_loss_876_composition "Hex(1) HexNAc(2) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1604
-name: Hex(5)Phos(1)
-def: "Hex(5) Phos." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=1&hex=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1604]
-xref: record_id "1604"
-xref: delta_mono_mass "890.230448"
-xref: delta_avge_mass "890.6829"
-xref: delta_composition "H O(3) P Hex(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:42:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_891_mono_mass "890.230448"
-xref: spec_1_neutral_loss_891_avge_mass "890.6829"
-xref: spec_1_neutral_loss_891_flag "false"
-xref: spec_1_neutral_loss_891_composition "H O(3) P Hex(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_891_mono_mass "890.230448"
-xref: spec_1_neutral_loss_891_avge_mass "890.6829"
-xref: spec_1_neutral_loss_891_flag "false"
-xref: spec_1_neutral_loss_891_composition "H O(3) P Hex(5)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1606
-name: dHex(2)Hex(1)HexNAc(1)Kdn(1)
-def: "DHex(2) Hex HexNAc Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=1&hexnac=1&kdn=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1606]
-xref: record_id "1606"
-xref: delta_mono_mass "907.316881"
-xref: delta_avge_mass "907.8182"
-xref: delta_composition "dHex(2) Hex HexNAc Kdn"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 15:57:48"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_908_mono_mass "907.316881"
-xref: spec_1_neutral_loss_908_avge_mass "907.8182"
-xref: spec_1_neutral_loss_908_flag "false"
-xref: spec_1_neutral_loss_908_composition "dHex(2) Hex HexNAc Kdn"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_908_mono_mass "907.316881"
-xref: spec_1_neutral_loss_908_avge_mass "907.8182"
-xref: spec_1_neutral_loss_908_flag "false"
-xref: spec_1_neutral_loss_908_composition "dHex(2) Hex HexNAc Kdn"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1607
-name: dHex(1)Hex(3)HexNAc(1)Sulf(1)
-def: "DHex Hex(3) HexNAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=3&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1607]
-xref: record_id "1607"
-xref: delta_mono_mass "915.252567"
-xref: delta_avge_mass "915.8187"
-xref: delta_composition "O(3) S dHex Hex(3) HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:28:48"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_916_mono_mass "915.252567"
-xref: spec_1_neutral_loss_916_avge_mass "915.8187"
-xref: spec_1_neutral_loss_916_flag "false"
-xref: spec_1_neutral_loss_916_composition "O(3) S dHex Hex(3) HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_916_mono_mass "915.252567"
-xref: spec_1_neutral_loss_916_avge_mass "915.8187"
-xref: spec_1_neutral_loss_916_flag "false"
-xref: spec_1_neutral_loss_916_composition "O(3) S dHex Hex(3) HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1608
-name: dHex(1)Hex(1)HexNAc(3)
-def: "DHex Hex HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=1&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1608]
-xref: record_id "1608"
-xref: delta_mono_mass "917.34885"
-xref: delta_avge_mass "917.8594"
-xref: delta_composition "dHex(1) Hex(1) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_918_mono_mass "917.34885"
-xref: spec_1_neutral_loss_918_avge_mass "917.8594"
-xref: spec_1_neutral_loss_918_flag "false"
-xref: spec_1_neutral_loss_918_composition "dHex(1) Hex(1) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_918_mono_mass "917.34885"
-xref: spec_1_neutral_loss_918_avge_mass "917.8594"
-xref: spec_1_neutral_loss_918_flag "false"
-xref: spec_1_neutral_loss_918_composition "dHex(1) Hex(1) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1609
-name: dHex(1)Hex(2)HexA(1)HexNAc(1)Sulf(1)
-def: "DHex Hex(2) HexA HexNAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=2&hexa=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1609]
-xref: record_id "1609"
-xref: delta_mono_mass "929.231831"
-xref: delta_avge_mass "929.8022"
-xref: delta_composition "O(3) S dHex Hex(2) HexA HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:28:59"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_930_mono_mass "929.231831"
-xref: spec_1_neutral_loss_930_avge_mass "929.8022"
-xref: spec_1_neutral_loss_930_flag "false"
-xref: spec_1_neutral_loss_930_composition "O(3) S dHex Hex(2) HexA HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_930_mono_mass "929.231831"
-xref: spec_1_neutral_loss_930_avge_mass "929.8022"
-xref: spec_1_neutral_loss_930_flag "false"
-xref: spec_1_neutral_loss_930_composition "O(3) S dHex Hex(2) HexA HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1610
-name: Hex(2)HexNAc(3)
-def: "Hex(2) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1610]
-xref: record_id "1610"
-xref: delta_mono_mass "933.343765"
-xref: delta_avge_mass "933.8588"
-xref: delta_composition "Hex(2) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-24 10:43:39"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_934_mono_mass "933.343765"
-xref: spec_1_neutral_loss_934_avge_mass "933.8588"
-xref: spec_1_neutral_loss_934_flag "false"
-xref: spec_1_neutral_loss_934_composition "Hex(2) HexNAc(3)"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_934_mono_mass "933.343765"
-xref: spec_1_neutral_loss_934_avge_mass "933.8588"
-xref: spec_1_neutral_loss_934_flag "false"
-xref: spec_1_neutral_loss_934_composition "Hex(2) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_934_mono_mass "933.343765"
-xref: spec_2_neutral_loss_934_avge_mass "933.8588"
-xref: spec_2_neutral_loss_934_flag "false"
-xref: spec_2_neutral_loss_934_composition "Hex(2) HexNAc(3)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1611
-name: Hex(1)HexNAc(2)NeuAc(1)Sulf(1)
-def: "Hex HexNAc(2) NeuAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=1&hexnac=2&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1611]
-xref: record_id "1611"
-xref: delta_mono_mass "939.2638"
-xref: delta_avge_mass "939.8434"
-xref: delta_composition "O(3) S Hex HexNAc(2) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:29:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_940_mono_mass "939.2638"
-xref: spec_1_neutral_loss_940_avge_mass "939.8434"
-xref: spec_1_neutral_loss_940_flag "false"
-xref: spec_1_neutral_loss_940_composition "O(3) S Hex HexNAc(2) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_940_mono_mass "939.2638"
-xref: spec_1_neutral_loss_940_avge_mass "939.8434"
-xref: spec_1_neutral_loss_940_flag "false"
-xref: spec_1_neutral_loss_940_composition "O(3) S Hex HexNAc(2) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1612
-name: dHex(2)Hex(4)
-def: "DHex(2) Hex(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1612]
-xref: record_id "1612"
-xref: delta_mono_mass "940.327112"
-xref: delta_avge_mass "940.8448"
-xref: delta_composition "dHex(2) Hex(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_941_mono_mass "940.327112"
-xref: spec_1_neutral_loss_941_avge_mass "940.8448"
-xref: spec_1_neutral_loss_941_flag "false"
-xref: spec_1_neutral_loss_941_composition "dHex(2) Hex(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_941_mono_mass "940.327112"
-xref: spec_1_neutral_loss_941_avge_mass "940.8448"
-xref: spec_1_neutral_loss_941_flag "false"
-xref: spec_1_neutral_loss_941_composition "dHex(2) Hex(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1614
-name: dHex(2)HexNAc(2)Kdn(1)
-def: "DHex(2) HexNAc(2) Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hexnac=2&kdn=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1614]
-xref: record_id "1614"
-xref: delta_mono_mass "948.34343"
-xref: delta_avge_mass "948.8701"
-xref: delta_composition "dHex(2) HexNAc(2) Kdn"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 15:57:42"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_949_mono_mass "948.34343"
-xref: spec_1_neutral_loss_949_avge_mass "948.8701"
-xref: spec_1_neutral_loss_949_flag "false"
-xref: spec_1_neutral_loss_949_composition "dHex(2) HexNAc(2) Kdn"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_949_mono_mass "948.34343"
-xref: spec_1_neutral_loss_949_avge_mass "948.8701"
-xref: spec_1_neutral_loss_949_flag "false"
-xref: spec_1_neutral_loss_949_composition "dHex(2) HexNAc(2) Kdn"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1615
-name: dHex(1)Hex(2)HexNAc(2)Sulf(1)
-def: "DHex Hex(2) HexNAc(2) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=2&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1615]
-xref: record_id "1615"
-xref: delta_mono_mass "956.279116"
-xref: delta_avge_mass "956.8706"
-xref: delta_composition "O(3) S dHex Hex(2) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:29:22"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_957_mono_mass "956.279116"
-xref: spec_1_neutral_loss_957_avge_mass "956.8706"
-xref: spec_1_neutral_loss_957_flag "false"
-xref: spec_1_neutral_loss_957_composition "O(3) S dHex Hex(2) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_957_mono_mass "956.279116"
-xref: spec_1_neutral_loss_957_avge_mass "956.8706"
-xref: spec_1_neutral_loss_957_flag "false"
-xref: spec_1_neutral_loss_957_composition "O(3) S dHex Hex(2) HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1616
-name: dHex(1)HexNAc(4)
-def: "DHex HexNAc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1616]
-xref: record_id "1616"
-xref: delta_mono_mass "958.375399"
-xref: delta_avge_mass "958.9113"
-xref: delta_composition "dHex(1) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_959_mono_mass "958.375399"
-xref: spec_1_neutral_loss_959_avge_mass "958.9113"
-xref: spec_1_neutral_loss_959_flag "false"
-xref: spec_1_neutral_loss_959_composition "dHex(1) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_959_mono_mass "958.375399"
-xref: spec_1_neutral_loss_959_avge_mass "958.9113"
-xref: spec_1_neutral_loss_959_flag "false"
-xref: spec_1_neutral_loss_959_composition "dHex(1) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1617
-name: Hex(1)HexNAc(1)NeuAc(1)NeuGc(1)
-def: "Hex HexNAc NeuAc NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=1&neuac=1&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1617]
-xref: record_id "1617"
-xref: delta_mono_mass "963.317944"
-xref: delta_avge_mass "963.8417"
-xref: delta_composition "Hex(1) HexNAc(1) NeuAc(1) NeuGc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_964_mono_mass "963.317944"
-xref: spec_1_neutral_loss_964_avge_mass "963.8417"
-xref: spec_1_neutral_loss_964_flag "false"
-xref: spec_1_neutral_loss_964_composition "Hex(1) HexNAc(1) NeuAc(1) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_964_mono_mass "963.317944"
-xref: spec_1_neutral_loss_964_avge_mass "963.8417"
-xref: spec_1_neutral_loss_964_flag "false"
-xref: spec_1_neutral_loss_964_composition "Hex(1) HexNAc(1) NeuAc(1) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1618
-name: dHex(1)Hex(1)HexNAc(2)Kdn(1)
-def: "DHex Hex HexNAc(2) Kdn ---OR--- Hex(2) HexNAc dHex NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=1&hexnac=2&kdn=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1618]
-xref: record_id "1618"
-xref: delta_mono_mass "964.338345"
-xref: delta_avge_mass "964.8695"
-xref: delta_composition "dHex Hex HexNAc(2) Kdn"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-17 11:43:59"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_965_mono_mass "964.338345"
-xref: spec_1_neutral_loss_965_avge_mass "964.8695"
-xref: spec_1_neutral_loss_965_flag "false"
-xref: spec_1_neutral_loss_965_composition "dHex Hex HexNAc(2) Kdn"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_965_mono_mass "964.338345"
-xref: spec_1_neutral_loss_965_avge_mass "964.8695"
-xref: spec_1_neutral_loss_965_flag "false"
-xref: spec_1_neutral_loss_965_composition "dHex Hex HexNAc(2) Kdn"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1619
-name: Hex(1)HexNAc(1)NeuGc(2)
-def: "Hex HexNAc NeuGc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=1&neugc=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1619]
-xref: record_id "1619"
-xref: delta_mono_mass "979.312859"
-xref: delta_avge_mass "979.8411"
-xref: delta_composition "Hex(1) HexNAc(1) NeuGc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_980_mono_mass "979.312859"
-xref: spec_1_neutral_loss_980_avge_mass "979.8411"
-xref: spec_1_neutral_loss_980_flag "false"
-xref: spec_1_neutral_loss_980_composition "Hex(1) HexNAc(1) NeuGc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_980_mono_mass "979.312859"
-xref: spec_1_neutral_loss_980_avge_mass "979.8411"
-xref: spec_1_neutral_loss_980_flag "false"
-xref: spec_1_neutral_loss_980_composition "Hex(1) HexNAc(1) NeuGc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1620
-name: Hex(1)HexNAc(1)NeuAc(2)Ac(1)
-def: "Ac Hex HexNAc NeuAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?acetyl=1&hex=1&hexnac=1&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1620]
-xref: record_id "1620"
-xref: delta_mono_mass "989.333594"
-xref: delta_avge_mass "989.879"
-xref: delta_composition "Ac Hex HexNAc NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:37:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_990_mono_mass "989.333594"
-xref: spec_1_neutral_loss_990_avge_mass "989.879"
-xref: spec_1_neutral_loss_990_flag "false"
-xref: spec_1_neutral_loss_990_composition "Ac Hex HexNAc NeuAc(2)"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_990_mono_mass "989.333594"
-xref: spec_1_neutral_loss_990_avge_mass "989.879"
-xref: spec_1_neutral_loss_990_flag "false"
-xref: spec_1_neutral_loss_990_composition "Ac Hex HexNAc NeuAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1621
-name: dHex(2)Hex(2)HexA(1)HexNAc(1)
-def: "DHex(2) Hex(2) HexA HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=2&hexa=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1621]
-xref: record_id "1621"
-xref: delta_mono_mass "995.332925"
-xref: delta_avge_mass "995.8802"
-xref: delta_composition "dHex(2) Hex(2) HexA(1) HexNAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_996_mono_mass "995.332925"
-xref: spec_1_neutral_loss_996_avge_mass "995.8802"
-xref: spec_1_neutral_loss_996_flag "false"
-xref: spec_1_neutral_loss_996_composition "dHex(2) Hex(2) HexA(1) HexNAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_996_mono_mass "995.332925"
-xref: spec_1_neutral_loss_996_avge_mass "995.8802"
-xref: spec_1_neutral_loss_996_flag "false"
-xref: spec_1_neutral_loss_996_composition "dHex(2) Hex(2) HexA(1) HexNAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1622
-name: dHex(1)Hex(1)HexNAc(3)Sulf(1)
-def: "DHex Hex HexNAc(3) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=1&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1622]
-xref: record_id "1622"
-xref: delta_mono_mass "997.305665"
-xref: delta_avge_mass "997.9226"
-xref: delta_composition "O(3) S dHex Hex HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:29:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_998_mono_mass "997.305665"
-xref: spec_1_neutral_loss_998_avge_mass "997.9226"
-xref: spec_1_neutral_loss_998_flag "false"
-xref: spec_1_neutral_loss_998_composition "O(3) S dHex Hex HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_998_mono_mass "997.305665"
-xref: spec_1_neutral_loss_998_avge_mass "997.9226"
-xref: spec_1_neutral_loss_998_flag "false"
-xref: spec_1_neutral_loss_998_composition "O(3) S dHex Hex HexNAc(3)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1623
-name: Hex(2)HexA(1)NeuAc(1)Pent(1)Sulf(1)
-def: "Hex(2) HexA NeuAc Pent Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&pent=1&hex=2&hexa=1&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1623]
-xref: record_id "1623"
-xref: delta_mono_mass "1003.232225"
-xref: delta_avge_mass "1003.8377"
-xref: delta_composition "O(3) S Pent Hex(2) HexA NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:29:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1004_mono_mass "1003.232225"
-xref: spec_1_neutral_loss_1004_avge_mass "1003.8377"
-xref: spec_1_neutral_loss_1004_flag "false"
-xref: spec_1_neutral_loss_1004_composition "O(3) S Pent Hex(2) HexA NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1004_mono_mass "1003.232225"
-xref: spec_1_neutral_loss_1004_avge_mass "1003.8377"
-xref: spec_1_neutral_loss_1004_flag "false"
-xref: spec_1_neutral_loss_1004_composition "O(3) S Pent Hex(2) HexA NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1624
-name: dHex(1)Hex(1)HexNAc(2)NeuAc(1)
-def: "DHex Hex HexNAc(2) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=1&hexnac=2&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1624]
-xref: record_id "1624"
-xref: delta_mono_mass "1005.364894"
-xref: delta_avge_mass "1005.9214"
-xref: delta_composition "dHex(1) Hex(1) HexNAc(2) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1006_mono_mass "1005.364894"
-xref: spec_1_neutral_loss_1006_avge_mass "1005.9214"
-xref: spec_1_neutral_loss_1006_flag "false"
-xref: spec_1_neutral_loss_1006_composition "dHex(1) Hex(1) HexNAc(2) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1006_mono_mass "1005.364894"
-xref: spec_1_neutral_loss_1006_avge_mass "1005.9214"
-xref: spec_1_neutral_loss_1006_flag "false"
-xref: spec_1_neutral_loss_1006_composition "dHex(1) Hex(1) HexNAc(2) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1625
-name: dHex(1)Hex(3)HexA(1)HexNAc(1)
-def: "DHex Hex(3) HexA HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexa=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1625]
-xref: record_id "1625"
-xref: delta_mono_mass "1011.32784"
-xref: delta_avge_mass "1011.8796"
-xref: delta_composition "dHex(1) Hex(3) HexA(1) HexNAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1012_mono_mass "1011.32784"
-xref: spec_1_neutral_loss_1012_avge_mass "1011.8796"
-xref: spec_1_neutral_loss_1012_flag "false"
-xref: spec_1_neutral_loss_1012_composition "dHex(1) Hex(3) HexA(1) HexNAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1012_mono_mass "1011.32784"
-xref: spec_1_neutral_loss_1012_avge_mass "1011.8796"
-xref: spec_1_neutral_loss_1012_flag "false"
-xref: spec_1_neutral_loss_1012_composition "dHex(1) Hex(3) HexA(1) HexNAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1626
-name: Hex(2)HexNAc(3)Sulf(1)
-def: "Hex(2) HexNAc(3) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=2&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1626]
-xref: record_id "1626"
-xref: delta_mono_mass "1013.300579"
-xref: delta_avge_mass "1013.922"
-xref: delta_composition "O(3) S Hex(2) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:30:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1014_mono_mass "1013.300579"
-xref: spec_1_neutral_loss_1014_avge_mass "1013.922"
-xref: spec_1_neutral_loss_1014_flag "false"
-xref: spec_1_neutral_loss_1014_composition "O(3) S Hex(2) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1014_mono_mass "1013.300579"
-xref: spec_1_neutral_loss_1014_avge_mass "1013.922"
-xref: spec_1_neutral_loss_1014_flag "false"
-xref: spec_1_neutral_loss_1014_composition "O(3) S Hex(2) HexNAc(3)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1627
-name: Hex(5)HexNAc(1)
-def: "Hex(5) HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=5&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1627]
-xref: record_id "1627"
-xref: delta_mono_mass "1013.34349"
-xref: delta_avge_mass "1013.8955"
-xref: delta_composition "Hex(5) HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-24 11:00:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1014_mono_mass "1013.34349"
-xref: spec_1_neutral_loss_1014_avge_mass "1013.8955"
-xref: spec_1_neutral_loss_1014_flag "false"
-xref: spec_1_neutral_loss_1014_composition "Hex(5) HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1014_mono_mass "1013.34349"
-xref: spec_1_neutral_loss_1014_avge_mass "1013.8955"
-xref: spec_1_neutral_loss_1014_flag "false"
-xref: spec_1_neutral_loss_1014_composition "Hex(5) HexNAc"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1014_mono_mass "1013.34349"
-xref: spec_2_neutral_loss_1014_avge_mass "1013.8955"
-xref: spec_2_neutral_loss_1014_flag "false"
-xref: spec_2_neutral_loss_1014_composition "Hex(5) HexNAc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1628
-name: HexNAc(5)
-def: "HexNAc(5)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1628]
-xref: record_id "1628"
-xref: delta_mono_mass "1015.396863"
-xref: delta_avge_mass "1015.9626"
-xref: delta_composition "HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1016_mono_mass "1015.396863"
-xref: spec_1_neutral_loss_1016_avge_mass "1015.9626"
-xref: spec_1_neutral_loss_1016_flag "false"
-xref: spec_1_neutral_loss_1016_composition "HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1016_mono_mass "1015.396863"
-xref: spec_1_neutral_loss_1016_avge_mass "1015.9626"
-xref: spec_1_neutral_loss_1016_flag "false"
-xref: spec_1_neutral_loss_1016_composition "HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1630
-name: Hex(1)HexNAc(1)NeuAc(2)Ac(2)
-def: "Ac(2) Hex HexNAc NeuAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?acetyl=2&hex=1&hexnac=1&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1630]
-xref: record_id "1630"
-xref: delta_mono_mass "1031.344159"
-xref: delta_avge_mass "1031.9156"
-xref: delta_composition "Ac(2) Hex HexNAc NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:38:10"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1032_mono_mass "1031.344159"
-xref: spec_1_neutral_loss_1032_avge_mass "1031.9156"
-xref: spec_1_neutral_loss_1032_flag "false"
-xref: spec_1_neutral_loss_1032_composition "Ac(2) Hex HexNAc NeuAc(2)"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1032_mono_mass "1031.344159"
-xref: spec_1_neutral_loss_1032_avge_mass "1031.9156"
-xref: spec_1_neutral_loss_1032_flag "false"
-xref: spec_1_neutral_loss_1032_composition "Ac(2) Hex HexNAc NeuAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1631
-name: Hex(2)HexNAc(2)NeuGc(1)
-def: "Hex(2) HexNAc(2) NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=2&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1631]
-xref: record_id "1631"
-xref: delta_mono_mass "1037.354723"
-xref: delta_avge_mass "1037.9202"
-xref: delta_composition "Hex(2) HexNAc(2) NeuGc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1038_mono_mass "1037.354723"
-xref: spec_1_neutral_loss_1038_avge_mass "1037.9202"
-xref: spec_1_neutral_loss_1038_flag "false"
-xref: spec_1_neutral_loss_1038_composition "Hex(2) HexNAc(2) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1038_mono_mass "1037.354723"
-xref: spec_1_neutral_loss_1038_avge_mass "1037.9202"
-xref: spec_1_neutral_loss_1038_flag "false"
-xref: spec_1_neutral_loss_1038_composition "Hex(2) HexNAc(2) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1632
-name: Hex(5)Phos(3)
-def: "Hex(5) Phos(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=3&hex=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1632]
-xref: record_id "1632"
-xref: delta_mono_mass "1050.16311"
-xref: delta_avge_mass "1050.6427"
-xref: delta_composition "H(3) O(9) P(3) Hex(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:42:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1051_mono_mass "1050.16311"
-xref: spec_1_neutral_loss_1051_avge_mass "1050.6427"
-xref: spec_1_neutral_loss_1051_flag "false"
-xref: spec_1_neutral_loss_1051_composition "H(3) O(9) P(3) Hex(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1051_mono_mass "1050.16311"
-xref: spec_1_neutral_loss_1051_avge_mass "1050.6427"
-xref: spec_1_neutral_loss_1051_flag "false"
-xref: spec_1_neutral_loss_1051_composition "H(3) O(9) P(3) Hex(5)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1633
-name: Hex(6)Phos(1)
-def: "Hex(6) Phos." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=1&hex=6&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1633]
-xref: record_id "1633"
-xref: delta_mono_mass "1052.283272"
-xref: delta_avge_mass "1052.8235"
-xref: delta_composition "H O(3) P Hex(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:42:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1053_mono_mass "1052.283272"
-xref: spec_1_neutral_loss_1053_avge_mass "1052.8235"
-xref: spec_1_neutral_loss_1053_flag "false"
-xref: spec_1_neutral_loss_1053_composition "H O(3) P Hex(6)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1053_mono_mass "1052.283272"
-xref: spec_1_neutral_loss_1053_avge_mass "1052.8235"
-xref: spec_1_neutral_loss_1053_flag "false"
-xref: spec_1_neutral_loss_1053_composition "H O(3) P Hex(6)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1634
-name: dHex(1)Hex(2)HexA(1)HexNAc(2)
-def: "DHex Hex(2) HexA HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=2&hexa=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1634]
-xref: record_id "1634"
-xref: delta_mono_mass "1052.354389"
-xref: delta_avge_mass "1052.9316"
-xref: delta_composition "dHex(1) Hex(2) HexA(1) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1053_mono_mass "1052.354389"
-xref: spec_1_neutral_loss_1053_avge_mass "1052.9316"
-xref: spec_1_neutral_loss_1053_flag "false"
-xref: spec_1_neutral_loss_1053_composition "dHex(1) Hex(2) HexA(1) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1053_mono_mass "1052.354389"
-xref: spec_1_neutral_loss_1053_avge_mass "1052.9316"
-xref: spec_1_neutral_loss_1053_flag "false"
-xref: spec_1_neutral_loss_1053_composition "dHex(1) Hex(2) HexA(1) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1635
-name: dHex(2)Hex(3)HexNAc(1)Sulf(1)
-def: "DHex(2) Hex(3) HexNAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=2&hex=3&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1635]
-xref: record_id "1635"
-xref: delta_mono_mass "1061.310475"
-xref: delta_avge_mass "1061.9599"
-xref: delta_composition "O(3) S dHex(2) Hex(3) HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:30:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1062_mono_mass "1061.310475"
-xref: spec_1_neutral_loss_1062_avge_mass "1061.9599"
-xref: spec_1_neutral_loss_1062_flag "false"
-xref: spec_1_neutral_loss_1062_composition "O(3) S dHex(2) Hex(3) HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1062_mono_mass "1061.310475"
-xref: spec_1_neutral_loss_1062_avge_mass "1061.9599"
-xref: spec_1_neutral_loss_1062_flag "false"
-xref: spec_1_neutral_loss_1062_composition "O(3) S dHex(2) Hex(3) HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1636
-name: Hex(1)HexNAc(3)NeuAc(1)
-def: "Hex HexNAc(3) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=3&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1636]
-xref: record_id "1636"
-xref: delta_mono_mass "1062.386358"
-xref: delta_avge_mass "1062.9727"
-xref: delta_composition "Hex(1) HexNAc(3) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1063_mono_mass "1062.386358"
-xref: spec_1_neutral_loss_1063_avge_mass "1062.9727"
-xref: spec_1_neutral_loss_1063_flag "false"
-xref: spec_1_neutral_loss_1063_composition "Hex(1) HexNAc(3) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1063_mono_mass "1062.386358"
-xref: spec_1_neutral_loss_1063_avge_mass "1062.9727"
-xref: spec_1_neutral_loss_1063_flag "false"
-xref: spec_1_neutral_loss_1063_composition "Hex(1) HexNAc(3) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1637
-name: dHex(2)Hex(1)HexNAc(3)
-def: "DHex(2) Hex HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=1&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1637]
-xref: record_id "1637"
-xref: delta_mono_mass "1063.406759"
-xref: delta_avge_mass "1064.0006"
-xref: delta_composition "dHex(2) Hex(1) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1064_mono_mass "1063.406759"
-xref: spec_1_neutral_loss_1064_avge_mass "1064.0006"
-xref: spec_1_neutral_loss_1064_flag "false"
-xref: spec_1_neutral_loss_1064_composition "dHex(2) Hex(1) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1064_mono_mass "1063.406759"
-xref: spec_1_neutral_loss_1064_avge_mass "1064.0006"
-xref: spec_1_neutral_loss_1064_flag "false"
-xref: spec_1_neutral_loss_1064_composition "dHex(2) Hex(1) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1638
-name: Hex(1)HexNAc(3)NeuGc(1)
-def: "Hex HexNAc(3) NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=3&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1638]
-xref: record_id "1638"
-xref: delta_mono_mass "1078.381273"
-xref: delta_avge_mass "1078.9721"
-xref: delta_composition "Hex(1) HexNAc(3) NeuGc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1079_mono_mass "1078.381273"
-xref: spec_1_neutral_loss_1079_avge_mass "1078.9721"
-xref: spec_1_neutral_loss_1079_flag "false"
-xref: spec_1_neutral_loss_1079_composition "Hex(1) HexNAc(3) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1079_mono_mass "1078.381273"
-xref: spec_1_neutral_loss_1079_avge_mass "1078.9721"
-xref: spec_1_neutral_loss_1079_flag "false"
-xref: spec_1_neutral_loss_1079_composition "Hex(1) HexNAc(3) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1639
-name: dHex(1)Hex(1)HexNAc(2)NeuAc(1)Sulf(1)
-def: "DHex Hex HexNAc(2) NeuAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=1&hexnac=2&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1639]
-xref: record_id "1639"
-xref: delta_mono_mass "1085.321709"
-xref: delta_avge_mass "1085.9846"
-xref: delta_composition "O(3) S dHex Hex HexNAc(2) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:30:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1086_mono_mass "1085.321709"
-xref: spec_1_neutral_loss_1086_avge_mass "1085.9846"
-xref: spec_1_neutral_loss_1086_flag "false"
-xref: spec_1_neutral_loss_1086_composition "O(3) S dHex Hex HexNAc(2) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1086_mono_mass "1085.321709"
-xref: spec_1_neutral_loss_1086_avge_mass "1085.9846"
-xref: spec_1_neutral_loss_1086_flag "false"
-xref: spec_1_neutral_loss_1086_composition "O(3) S dHex Hex HexNAc(2) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1640
-name: dHex(1)Hex(3)HexA(1)HexNAc(1)Sulf(1)
-def: "DHex Hex(3) HexA HexNAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=3&hexa=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1640]
-xref: record_id "1640"
-xref: delta_mono_mass "1091.284655"
-xref: delta_avge_mass "1091.9428"
-xref: delta_composition "O(3) S dHex Hex(3) HexA HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:30:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1092_mono_mass "1091.284655"
-xref: spec_1_neutral_loss_1092_avge_mass "1091.9428"
-xref: spec_1_neutral_loss_1092_flag "false"
-xref: spec_1_neutral_loss_1092_composition "O(3) S dHex Hex(3) HexA HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1092_mono_mass "1091.284655"
-xref: spec_1_neutral_loss_1092_avge_mass "1091.9428"
-xref: spec_1_neutral_loss_1092_flag "false"
-xref: spec_1_neutral_loss_1092_composition "O(3) S dHex Hex(3) HexA HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1641
-name: dHex(1)Hex(1)HexA(1)HexNAc(3)
-def: "DHex Hex HexA HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=1&hexa=1&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1641]
-xref: record_id "1641"
-xref: delta_mono_mass "1093.380938"
-xref: delta_avge_mass "1093.9835"
-xref: delta_composition "dHex(1) Hex(1) HexA(1) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1094_mono_mass "1093.380938"
-xref: spec_1_neutral_loss_1094_avge_mass "1093.9835"
-xref: spec_1_neutral_loss_1094_flag "false"
-xref: spec_1_neutral_loss_1094_composition "dHex(1) Hex(1) HexA(1) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1094_mono_mass "1093.380938"
-xref: spec_1_neutral_loss_1094_avge_mass "1093.9835"
-xref: spec_1_neutral_loss_1094_flag "false"
-xref: spec_1_neutral_loss_1094_composition "dHex(1) Hex(1) HexA(1) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1642
-name: Hex(2)HexNAc(2)NeuAc(1)Sulf(1)
-def: "Hex(2) HexNAc(2) NeuAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=2&hexnac=2&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1642]
-xref: record_id "1642"
-xref: delta_mono_mass "1101.316623"
-xref: delta_avge_mass "1101.984"
-xref: delta_composition "O(3) S Hex(2) HexNAc(2) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:30:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1102_mono_mass "1101.316623"
-xref: spec_1_neutral_loss_1102_avge_mass "1101.984"
-xref: spec_1_neutral_loss_1102_flag "false"
-xref: spec_1_neutral_loss_1102_composition "O(3) S Hex(2) HexNAc(2) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1102_mono_mass "1101.316623"
-xref: spec_1_neutral_loss_1102_avge_mass "1101.984"
-xref: spec_1_neutral_loss_1102_flag "false"
-xref: spec_1_neutral_loss_1102_composition "O(3) S Hex(2) HexNAc(2) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1643
-name: dHex(2)Hex(2)HexNAc(2)Sulf(1)
-def: "DHex(2) Hex(2) HexNAc(2) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=2&hex=2&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1643]
-xref: record_id "1643"
-xref: delta_mono_mass "1102.337025"
-xref: delta_avge_mass "1103.0118"
-xref: delta_composition "O(3) S dHex(2) Hex(2) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:31:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1103_mono_mass "1102.337025"
-xref: spec_1_neutral_loss_1103_avge_mass "1103.0118"
-xref: spec_1_neutral_loss_1103_flag "false"
-xref: spec_1_neutral_loss_1103_composition "O(3) S dHex(2) Hex(2) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1103_mono_mass "1102.337025"
-xref: spec_1_neutral_loss_1103_avge_mass "1103.0118"
-xref: spec_1_neutral_loss_1103_flag "false"
-xref: spec_1_neutral_loss_1103_composition "O(3) S dHex(2) Hex(2) HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1644
-name: dHex(2)Hex(1)HexNAc(2)Kdn(1)
-def: "DHex(2) Hex HexNAc(2) Kdn ---OR--- Hex(2) HexNAc dHex(2) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=1&hexnac=2&kdn=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1644]
-xref: record_id "1644"
-xref: delta_mono_mass "1110.396254"
-xref: delta_avge_mass "1111.0107"
-xref: delta_composition "dHex(2) Hex HexNAc(2) Kdn"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-17 12:14:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1111_mono_mass "1110.396254"
-xref: spec_1_neutral_loss_1111_avge_mass "1111.0107"
-xref: spec_1_neutral_loss_1111_flag "false"
-xref: spec_1_neutral_loss_1111_composition "dHex(2) Hex HexNAc(2) Kdn"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1111_mono_mass "1110.396254"
-xref: spec_1_neutral_loss_1111_avge_mass "1111.0107"
-xref: spec_1_neutral_loss_1111_flag "false"
-xref: spec_1_neutral_loss_1111_composition "dHex(2) Hex HexNAc(2) Kdn"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1645
-name: dHex(1)Hex(1)HexNAc(4)
-def: "DHex Hex HexNAc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=1&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1645]
-xref: record_id "1645"
-xref: delta_mono_mass "1120.428223"
-xref: delta_avge_mass "1121.0519"
-xref: delta_composition "dHex(1) Hex(1) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1121_mono_mass "1120.428223"
-xref: spec_1_neutral_loss_1121_avge_mass "1121.0519"
-xref: spec_1_neutral_loss_1121_flag "false"
-xref: spec_1_neutral_loss_1121_composition "dHex(1) Hex(1) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1121_mono_mass "1120.428223"
-xref: spec_1_neutral_loss_1121_avge_mass "1121.0519"
-xref: spec_1_neutral_loss_1121_flag "false"
-xref: spec_1_neutral_loss_1121_composition "dHex(1) Hex(1) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1646
-name: Hex(2)HexNAc(4)
-def: "Hex(2) HexNAc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1646]
-xref: record_id "1646"
-xref: delta_mono_mass "1136.423137"
-xref: delta_avge_mass "1137.0513"
-xref: delta_composition "Hex(2) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-24 11:06:46"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1137_mono_mass "1136.423137"
-xref: spec_1_neutral_loss_1137_avge_mass "1137.0513"
-xref: spec_1_neutral_loss_1137_flag "false"
-xref: spec_1_neutral_loss_1137_composition "Hex(2) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1137_mono_mass "1136.423137"
-xref: spec_1_neutral_loss_1137_avge_mass "1137.0513"
-xref: spec_1_neutral_loss_1137_flag "false"
-xref: spec_1_neutral_loss_1137_composition "Hex(2) HexNAc(4)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1137_mono_mass "1136.423137"
-xref: spec_2_neutral_loss_1137_avge_mass "1137.0513"
-xref: spec_2_neutral_loss_1137_flag "false"
-xref: spec_2_neutral_loss_1137_composition "Hex(2) HexNAc(4)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1647
-name: Hex(2)HexNAc(1)NeuGc(2)
-def: "Hex(2) HexNAc NeuGc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=1&neugc=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1647]
-xref: record_id "1647"
-xref: delta_mono_mass "1141.365682"
-xref: delta_avge_mass "1141.9817"
-xref: delta_composition "Hex(2) HexNAc(1) NeuGc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1142_mono_mass "1141.365682"
-xref: spec_1_neutral_loss_1142_avge_mass "1141.9817"
-xref: spec_1_neutral_loss_1142_flag "false"
-xref: spec_1_neutral_loss_1142_composition "Hex(2) HexNAc(1) NeuGc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1142_mono_mass "1141.365682"
-xref: spec_1_neutral_loss_1142_avge_mass "1141.9817"
-xref: spec_1_neutral_loss_1142_flag "false"
-xref: spec_1_neutral_loss_1142_composition "Hex(2) HexNAc(1) NeuGc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1648
-name: dHex(2)Hex(4)HexNAc(1)
-def: "DHex(2) Hex(4) HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=4&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1648]
-xref: record_id "1648"
-xref: delta_mono_mass "1143.406484"
-xref: delta_avge_mass "1144.0373"
-xref: delta_composition "dHex(2) Hex(4) HexNAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1144_mono_mass "1143.406484"
-xref: spec_1_neutral_loss_1144_avge_mass "1144.0373"
-xref: spec_1_neutral_loss_1144_flag "false"
-xref: spec_1_neutral_loss_1144_composition "dHex(2) Hex(4) HexNAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1144_mono_mass "1143.406484"
-xref: spec_1_neutral_loss_1144_avge_mass "1144.0373"
-xref: spec_1_neutral_loss_1144_flag "false"
-xref: spec_1_neutral_loss_1144_composition "dHex(2) Hex(4) HexNAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1649
-name: Hex(1)HexNAc(2)NeuAc(2)
-def: "Hex HexNAc(2) NeuAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=2&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1649]
-xref: record_id "1649"
-xref: delta_mono_mass "1150.402402"
-xref: delta_avge_mass "1151.0348"
-xref: delta_composition "Hex(1) HexNAc(2) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1151_mono_mass "1150.402402"
-xref: spec_1_neutral_loss_1151_avge_mass "1151.0348"
-xref: spec_1_neutral_loss_1151_flag "false"
-xref: spec_1_neutral_loss_1151_composition "Hex(1) HexNAc(2) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1151_mono_mass "1150.402402"
-xref: spec_1_neutral_loss_1151_avge_mass "1151.0348"
-xref: spec_1_neutral_loss_1151_flag "false"
-xref: spec_1_neutral_loss_1151_composition "Hex(1) HexNAc(2) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1650
-name: dHex(2)Hex(1)HexNAc(2)NeuAc(1)
-def: "DHex(2) Hex HexNAc(2) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=1&hexnac=2&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1650]
-xref: record_id "1650"
-xref: delta_mono_mass "1151.422803"
-xref: delta_avge_mass "1152.0626"
-xref: delta_composition "dHex(2) Hex(1) HexNAc(2) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1152_mono_mass "1151.422803"
-xref: spec_1_neutral_loss_1152_avge_mass "1152.0626"
-xref: spec_1_neutral_loss_1152_flag "false"
-xref: spec_1_neutral_loss_1152_composition "dHex(2) Hex(1) HexNAc(2) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1152_mono_mass "1151.422803"
-xref: spec_1_neutral_loss_1152_avge_mass "1152.0626"
-xref: spec_1_neutral_loss_1152_flag "false"
-xref: spec_1_neutral_loss_1152_composition "dHex(2) Hex(1) HexNAc(2) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1651
-name: dHex(1)Hex(2)HexNAc(3)Sulf(1)
-def: "DHex Hex(2) HexNAc(3) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=2&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1651]
-xref: record_id "1651"
-xref: delta_mono_mass "1159.358488"
-xref: delta_avge_mass "1160.0632"
-xref: delta_composition "O(3) S dHex Hex(2) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:31:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1160_mono_mass "1159.358488"
-xref: spec_1_neutral_loss_1160_avge_mass "1160.0632"
-xref: spec_1_neutral_loss_1160_flag "false"
-xref: spec_1_neutral_loss_1160_composition "O(3) S dHex Hex(2) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1160_mono_mass "1159.358488"
-xref: spec_1_neutral_loss_1160_avge_mass "1160.0632"
-xref: spec_1_neutral_loss_1160_flag "false"
-xref: spec_1_neutral_loss_1160_composition "O(3) S dHex Hex(2) HexNAc(3)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1652
-name: dHex(1)HexNAc(5)
-def: "DHex HexNAc(5)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1652]
-xref: record_id "1652"
-xref: delta_mono_mass "1161.454772"
-xref: delta_avge_mass "1162.1038"
-xref: delta_composition "dHex(1) HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1162_mono_mass "1161.454772"
-xref: spec_1_neutral_loss_1162_avge_mass "1162.1038"
-xref: spec_1_neutral_loss_1162_flag "false"
-xref: spec_1_neutral_loss_1162_composition "dHex(1) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1162_mono_mass "1161.454772"
-xref: spec_1_neutral_loss_1162_avge_mass "1162.1038"
-xref: spec_1_neutral_loss_1162_flag "false"
-xref: spec_1_neutral_loss_1162_composition "dHex(1) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1653
-name: dHex(2)Hex(1)HexNAc(2)NeuGc(1)
-def: "DHex(2) Hex HexNAc(2) NeuGc ---OR--- Hex(2) HexNAc(2) dHex NeuAc ---OR--- Hex HexNAc(3) dHex Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=1&hexnac=2&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1653]
-xref: record_id "1653"
-xref: delta_mono_mass "1167.417718"
-xref: delta_avge_mass "1168.062"
-xref: delta_composition "dHex(2) Hex HexNAc(2) NeuGc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-17 12:18:14"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1168_mono_mass "1167.417718"
-xref: spec_1_neutral_loss_1168_avge_mass "1168.062"
-xref: spec_1_neutral_loss_1168_flag "false"
-xref: spec_1_neutral_loss_1168_composition "dHex(2) Hex HexNAc(2) NeuGc"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1168_mono_mass "1167.417718"
-xref: spec_1_neutral_loss_1168_avge_mass "1168.062"
-xref: spec_1_neutral_loss_1168_flag "false"
-xref: spec_1_neutral_loss_1168_composition "dHex(2) Hex HexNAc(2) NeuGc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1654
-name: dHex(3)Hex(2)HexNAc(2)
-def: "DHex(3) Hex(2) HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=3&hex=2&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1654]
-xref: record_id "1654"
-xref: delta_mono_mass "1168.438119"
-xref: delta_avge_mass "1169.0898"
-xref: delta_composition "dHex(3) Hex(2) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1169_mono_mass "1168.438119"
-xref: spec_1_neutral_loss_1169_avge_mass "1169.0898"
-xref: spec_1_neutral_loss_1169_flag "false"
-xref: spec_1_neutral_loss_1169_composition "dHex(3) Hex(2) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1169_mono_mass "1168.438119"
-xref: spec_1_neutral_loss_1169_avge_mass "1169.0898"
-xref: spec_1_neutral_loss_1169_flag "false"
-xref: spec_1_neutral_loss_1169_composition "dHex(3) Hex(2) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1655
-name: Hex(3)HexNAc(3)Sulf(1)
-def: "Hex(3) HexNAc(3) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=3&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1655]
-xref: record_id "1655"
-xref: delta_mono_mass "1175.353403"
-xref: delta_avge_mass "1176.0626"
-xref: delta_composition "O(3) S Hex(3) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-24 11:08:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1176_mono_mass "1175.353403"
-xref: spec_1_neutral_loss_1176_avge_mass "1176.0626"
-xref: spec_1_neutral_loss_1176_flag "false"
-xref: spec_1_neutral_loss_1176_composition "O(3) S Hex(3) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1176_mono_mass "1175.353403"
-xref: spec_1_neutral_loss_1176_avge_mass "1176.0626"
-xref: spec_1_neutral_loss_1176_flag "false"
-xref: spec_1_neutral_loss_1176_composition "O(3) S Hex(3) HexNAc(3)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1176_mono_mass "1175.353403"
-xref: spec_2_neutral_loss_1176_avge_mass "1176.0626"
-xref: spec_2_neutral_loss_1176_flag "false"
-xref: spec_2_neutral_loss_1176_composition "O(3) S Hex(3) HexNAc(3)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1656
-name: dHex(2)Hex(2)HexNAc(2)Sulf(2)
-def: "DHex(2) Hex(2) HexNAc(2) Sulf(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=2&dhex=2&hex=2&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1656]
-xref: record_id "1656"
-xref: delta_mono_mass "1182.293839"
-xref: delta_avge_mass "1183.075"
-xref: delta_composition "O(6) S(2) dHex(2) Hex(2) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:31:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1183_mono_mass "1182.293839"
-xref: spec_1_neutral_loss_1183_avge_mass "1183.075"
-xref: spec_1_neutral_loss_1183_flag "false"
-xref: spec_1_neutral_loss_1183_composition "O(6) S(2) dHex(2) Hex(2) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1183_mono_mass "1182.293839"
-xref: spec_1_neutral_loss_1183_avge_mass "1183.075"
-xref: spec_1_neutral_loss_1183_flag "false"
-xref: spec_1_neutral_loss_1183_composition "O(6) S(2) dHex(2) Hex(2) HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1657
-name: dHex(1)Hex(2)HexNAc(2)NeuGc(1)
-def: "DHex Hex(2) HexNAc(2) NeuGc ---OR--- Hex(3) HexNAc(2) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=2&hexnac=2&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1657]
-xref: record_id "1657"
-xref: delta_mono_mass "1183.412632"
-xref: delta_avge_mass "1184.0614"
-xref: delta_composition "dHex Hex(2) HexNAc(2) NeuGc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-17 13:10:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1184_mono_mass "1183.412632"
-xref: spec_1_neutral_loss_1184_avge_mass "1184.0614"
-xref: spec_1_neutral_loss_1184_flag "false"
-xref: spec_1_neutral_loss_1184_composition "dHex Hex(2) HexNAc(2) NeuGc"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1184_mono_mass "1183.412632"
-xref: spec_1_neutral_loss_1184_avge_mass "1184.0614"
-xref: spec_1_neutral_loss_1184_flag "false"
-xref: spec_1_neutral_loss_1184_composition "dHex Hex(2) HexNAc(2) NeuGc"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1184_mono_mass "1183.412632"
-xref: spec_2_neutral_loss_1184_avge_mass "1184.0614"
-xref: spec_2_neutral_loss_1184_flag "false"
-xref: spec_2_neutral_loss_1184_composition "dHex Hex(2) HexNAc(2) NeuGc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1658
-name: dHex(1)Hex(1)HexNAc(3)NeuAc(1)
-def: "DHex Hex HexNAc(3) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=1&hexnac=3&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1658]
-xref: record_id "1658"
-xref: delta_mono_mass "1208.444267"
-xref: delta_avge_mass "1209.1139"
-xref: delta_composition "dHex Hex HexNAc(3) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-23 14:50:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1209_mono_mass "1208.444267"
-xref: spec_1_neutral_loss_1209_avge_mass "1209.1139"
-xref: spec_1_neutral_loss_1209_flag "false"
-xref: spec_1_neutral_loss_1209_composition "dHex Hex HexNAc(3) NeuAc"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1209_mono_mass "1208.444267"
-xref: spec_1_neutral_loss_1209_avge_mass "1209.1139"
-xref: spec_1_neutral_loss_1209_flag "false"
-xref: spec_1_neutral_loss_1209_composition "dHex Hex HexNAc(3) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1659
-name: Hex(6)Phos(3)
-def: "Hex(6) Phos(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=3&hex=6&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1659]
-xref: record_id "1659"
-xref: delta_mono_mass "1212.215934"
-xref: delta_avge_mass "1212.7833"
-xref: delta_composition "H(3) O(9) P(3) Hex(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:42:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1213_mono_mass "1212.215934"
-xref: spec_1_neutral_loss_1213_avge_mass "1212.7833"
-xref: spec_1_neutral_loss_1213_flag "false"
-xref: spec_1_neutral_loss_1213_composition "H(3) O(9) P(3) Hex(6)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1213_mono_mass "1212.215934"
-xref: spec_1_neutral_loss_1213_avge_mass "1212.7833"
-xref: spec_1_neutral_loss_1213_flag "false"
-xref: spec_1_neutral_loss_1213_composition "H(3) O(9) P(3) Hex(6)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1660
-name: dHex(1)Hex(3)HexA(1)HexNAc(2)
-def: "DHex Hex(3) HexA HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexa=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1660]
-xref: record_id "1660"
-xref: delta_mono_mass "1214.407213"
-xref: delta_avge_mass "1215.0722"
-xref: delta_composition "dHex(1) Hex(3) HexA(1) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1215_mono_mass "1214.407213"
-xref: spec_1_neutral_loss_1215_avge_mass "1215.0722"
-xref: spec_1_neutral_loss_1215_flag "false"
-xref: spec_1_neutral_loss_1215_composition "dHex(1) Hex(3) HexA(1) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1215_mono_mass "1214.407213"
-xref: spec_1_neutral_loss_1215_avge_mass "1215.0722"
-xref: spec_1_neutral_loss_1215_flag "false"
-xref: spec_1_neutral_loss_1215_composition "dHex(1) Hex(3) HexA(1) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1661
-name: dHex(1)Hex(1)HexNAc(3)NeuGc(1)
-def: "DHex Hex HexNAc(3) NeuGc ---OR--- Hex(2) HexNAc(3) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=1&hexnac=3&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1661]
-xref: record_id "1661"
-xref: delta_mono_mass "1224.439181"
-xref: delta_avge_mass "1225.1133"
-xref: delta_composition "dHex Hex HexNAc(3) NeuGc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-17 13:15:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1225_mono_mass "1224.439181"
-xref: spec_1_neutral_loss_1225_avge_mass "1225.1133"
-xref: spec_1_neutral_loss_1225_flag "false"
-xref: spec_1_neutral_loss_1225_composition "dHex Hex HexNAc(3) NeuGc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1225_mono_mass "1224.439181"
-xref: spec_1_neutral_loss_1225_avge_mass "1225.1133"
-xref: spec_1_neutral_loss_1225_flag "false"
-xref: spec_1_neutral_loss_1225_composition "dHex Hex HexNAc(3) NeuGc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1662
-name: Hex(1)HexNAc(2)NeuAc(2)Sulf(1)
-def: "Hex HexNAc(2) NeuAc(2) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=1&hexnac=2&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1662]
-xref: record_id "1662"
-xref: delta_mono_mass "1230.359217"
-xref: delta_avge_mass "1231.098"
-xref: delta_composition "O(3) S Hex HexNAc(2) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:31:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1231_mono_mass "1230.359217"
-xref: spec_1_neutral_loss_1231_avge_mass "1231.098"
-xref: spec_1_neutral_loss_1231_flag "false"
-xref: spec_1_neutral_loss_1231_composition "O(3) S Hex HexNAc(2) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1231_mono_mass "1230.359217"
-xref: spec_1_neutral_loss_1231_avge_mass "1231.098"
-xref: spec_1_neutral_loss_1231_flag "false"
-xref: spec_1_neutral_loss_1231_composition "O(3) S Hex HexNAc(2) NeuAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1663
-name: dHex(2)Hex(3)HexA(1)HexNAc(1)Sulf(1)
-def: "DHex(2) Hex(3) HexA HexNAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=2&hex=3&hexa=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1663]
-xref: record_id "1663"
-xref: delta_mono_mass "1237.342563"
-xref: delta_avge_mass "1238.084"
-xref: delta_composition "O(3) S dHex(2) Hex(3) HexA HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:32:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1238_mono_mass "1237.342563"
-xref: spec_1_neutral_loss_1238_avge_mass "1238.084"
-xref: spec_1_neutral_loss_1238_flag "false"
-xref: spec_1_neutral_loss_1238_composition "O(3) S dHex(2) Hex(3) HexA HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1238_mono_mass "1237.342563"
-xref: spec_1_neutral_loss_1238_avge_mass "1238.084"
-xref: spec_1_neutral_loss_1238_flag "false"
-xref: spec_1_neutral_loss_1238_composition "O(3) S dHex(2) Hex(3) HexA HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1664
-name: Hex(1)HexNAc(1)NeuAc(3)
-def: "Hex HexNAc NeuAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=1&neuac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1664]
-xref: record_id "1664"
-xref: delta_mono_mass "1238.418446"
-xref: delta_avge_mass "1239.0969"
-xref: delta_composition "Hex(1) HexNAc(1) NeuAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1239_mono_mass "1238.418446"
-xref: spec_1_neutral_loss_1239_avge_mass "1239.0969"
-xref: spec_1_neutral_loss_1239_flag "false"
-xref: spec_1_neutral_loss_1239_composition "Hex(1) HexNAc(1) NeuAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1239_mono_mass "1238.418446"
-xref: spec_1_neutral_loss_1239_avge_mass "1239.0969"
-xref: spec_1_neutral_loss_1239_flag "false"
-xref: spec_1_neutral_loss_1239_composition "Hex(1) HexNAc(1) NeuAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1665
-name: Hex(2)HexNAc(3)NeuGc(1)
-def: "Hex(2) HexNAc(3) NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=3&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1665]
-xref: record_id "1665"
-xref: delta_mono_mass "1240.434096"
-xref: delta_avge_mass "1241.1127"
-xref: delta_composition "Hex(2) HexNAc(3) NeuGc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1241_mono_mass "1240.434096"
-xref: spec_1_neutral_loss_1241_avge_mass "1241.1127"
-xref: spec_1_neutral_loss_1241_flag "false"
-xref: spec_1_neutral_loss_1241_composition "Hex(2) HexNAc(3) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1241_mono_mass "1240.434096"
-xref: spec_1_neutral_loss_1241_avge_mass "1241.1127"
-xref: spec_1_neutral_loss_1241_flag "false"
-xref: spec_1_neutral_loss_1241_composition "Hex(2) HexNAc(3) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1666
-name: dHex(1)Hex(2)HexNAc(2)NeuAc(1)Sulf(1)
-def: "DHex Hex(2) HexNAc(2) NeuAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=2&hexnac=2&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1666]
-xref: record_id "1666"
-xref: delta_mono_mass "1247.374532"
-xref: delta_avge_mass "1248.1252"
-xref: delta_composition "O(3) S dHex Hex(2) HexNAc(2) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:32:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1248_mono_mass "1247.374532"
-xref: spec_1_neutral_loss_1248_avge_mass "1248.1252"
-xref: spec_1_neutral_loss_1248_flag "false"
-xref: spec_1_neutral_loss_1248_composition "O(3) S dHex Hex(2) HexNAc(2) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1248_mono_mass "1247.374532"
-xref: spec_1_neutral_loss_1248_avge_mass "1248.1252"
-xref: spec_1_neutral_loss_1248_flag "false"
-xref: spec_1_neutral_loss_1248_composition "O(3) S dHex Hex(2) HexNAc(2) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1667
-name: dHex(3)Hex(1)HexNAc(2)Kdn(1)
-def: "DHex(3) Hex HexNAc(2) Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=3&hex=1&hexnac=2&kdn=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1667]
-xref: record_id "1667"
-xref: delta_mono_mass "1256.454163"
-xref: delta_avge_mass "1257.1519"
-xref: delta_composition "dHex(3) Hex HexNAc(2) Kdn"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 15:57:10"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1257_mono_mass "1256.454163"
-xref: spec_1_neutral_loss_1257_avge_mass "1257.1519"
-xref: spec_1_neutral_loss_1257_flag "false"
-xref: spec_1_neutral_loss_1257_composition "dHex(3) Hex HexNAc(2) Kdn"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1257_mono_mass "1256.454163"
-xref: spec_1_neutral_loss_1257_avge_mass "1257.1519"
-xref: spec_1_neutral_loss_1257_flag "false"
-xref: spec_1_neutral_loss_1257_composition "dHex(3) Hex HexNAc(2) Kdn"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1668
-name: dHex(2)Hex(3)HexNAc(2)Sulf(1)
-def: "DHex(2) Hex(3) HexNAc(2) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=2&hex=3&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1668]
-xref: record_id "1668"
-xref: delta_mono_mass "1264.389848"
-xref: delta_avge_mass "1265.1524"
-xref: delta_composition "O(3) S dHex(2) Hex(3) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:32:32"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1265_mono_mass "1264.389848"
-xref: spec_1_neutral_loss_1265_avge_mass "1265.1524"
-xref: spec_1_neutral_loss_1265_flag "false"
-xref: spec_1_neutral_loss_1265_composition "O(3) S dHex(2) Hex(3) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1265_mono_mass "1264.389848"
-xref: spec_1_neutral_loss_1265_avge_mass "1265.1524"
-xref: spec_1_neutral_loss_1265_flag "false"
-xref: spec_1_neutral_loss_1265_composition "O(3) S dHex(2) Hex(3) HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1669
-name: dHex(2)Hex(2)HexNAc(2)Kdn(1)
-def: "DHex(2) Hex(2) HexNAc(2) Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=2&hexnac=2&kdn=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1669]
-xref: record_id "1669"
-xref: delta_mono_mass "1272.449077"
-xref: delta_avge_mass "1273.1513"
-xref: delta_composition "dHex(2) Hex(2) HexNAc(2) Kdn"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 15:56:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1273_mono_mass "1272.449077"
-xref: spec_1_neutral_loss_1273_avge_mass "1273.1513"
-xref: spec_1_neutral_loss_1273_flag "false"
-xref: spec_1_neutral_loss_1273_composition "dHex(2) Hex(2) HexNAc(2) Kdn"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1273_mono_mass "1272.449077"
-xref: spec_1_neutral_loss_1273_avge_mass "1273.1513"
-xref: spec_1_neutral_loss_1273_flag "false"
-xref: spec_1_neutral_loss_1273_composition "dHex(2) Hex(2) HexNAc(2) Kdn"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1670
-name: dHex(2)Hex(2)HexA(1)HexNAc(2)Sulf(1)
-def: "DHex(2) Hex(2) HexA HexNAc(2) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=2&hex=2&hexa=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1670]
-xref: record_id "1670"
-xref: delta_mono_mass "1278.369113"
-xref: delta_avge_mass "1279.136"
-xref: delta_composition "O(3) S dHex(2) Hex(2) HexA HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:32:43"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1279_mono_mass "1278.369113"
-xref: spec_1_neutral_loss_1279_avge_mass "1279.136"
-xref: spec_1_neutral_loss_1279_flag "false"
-xref: spec_1_neutral_loss_1279_composition "O(3) S dHex(2) Hex(2) HexA HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1279_mono_mass "1278.369113"
-xref: spec_1_neutral_loss_1279_avge_mass "1279.136"
-xref: spec_1_neutral_loss_1279_flag "false"
-xref: spec_1_neutral_loss_1279_composition "O(3) S dHex(2) Hex(2) HexA HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1671
-name: dHex(1)Hex(2)HexNAc(4)
-def: "DHex Hex(2) HexNAc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=2&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1671]
-xref: record_id "1671"
-xref: delta_mono_mass "1282.481046"
-xref: delta_avge_mass "1283.1925"
-xref: delta_composition "dHex Hex(2) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-24 12:00:46"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1283_mono_mass "1282.481046"
-xref: spec_1_neutral_loss_1283_avge_mass "1283.1925"
-xref: spec_1_neutral_loss_1283_flag "false"
-xref: spec_1_neutral_loss_1283_composition "dHex Hex(2) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1283_mono_mass "1282.481046"
-xref: spec_1_neutral_loss_1283_avge_mass "1283.1925"
-xref: spec_1_neutral_loss_1283_flag "false"
-xref: spec_1_neutral_loss_1283_composition "dHex Hex(2) HexNAc(4)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1283_mono_mass "1282.481046"
-xref: spec_2_neutral_loss_1283_avge_mass "1283.1925"
-xref: spec_2_neutral_loss_1283_flag "false"
-xref: spec_2_neutral_loss_1283_composition "dHex Hex(2) HexNAc(4)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1672
-name: Hex(1)HexNAc(1)NeuGc(3)
-def: "Hex HexNAc NeuGc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=1&neugc=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1672]
-xref: record_id "1672"
-xref: delta_mono_mass "1286.40319"
-xref: delta_avge_mass "1287.0951"
-xref: delta_composition "Hex(1) HexNAc(1) NeuGc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1287_mono_mass "1286.40319"
-xref: spec_1_neutral_loss_1287_avge_mass "1287.0951"
-xref: spec_1_neutral_loss_1287_flag "false"
-xref: spec_1_neutral_loss_1287_composition "Hex(1) HexNAc(1) NeuGc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1287_mono_mass "1286.40319"
-xref: spec_1_neutral_loss_1287_avge_mass "1287.0951"
-xref: spec_1_neutral_loss_1287_flag "false"
-xref: spec_1_neutral_loss_1287_composition "Hex(1) HexNAc(1) NeuGc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1673
-name: dHex(1)Hex(1)HexNAc(3)NeuAc(1)Sulf(1)
-def: "DHex Hex HexNAc(3) NeuAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=1&hexnac=3&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1673]
-xref: record_id "1673"
-xref: delta_mono_mass "1288.401081"
-xref: delta_avge_mass "1289.1771"
-xref: delta_composition "O(3) S dHex Hex HexNAc(3) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:32:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1289_mono_mass "1288.401081"
-xref: spec_1_neutral_loss_1289_avge_mass "1289.1771"
-xref: spec_1_neutral_loss_1289_flag "false"
-xref: spec_1_neutral_loss_1289_composition "O(3) S dHex Hex HexNAc(3) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1289_mono_mass "1288.401081"
-xref: spec_1_neutral_loss_1289_avge_mass "1289.1771"
-xref: spec_1_neutral_loss_1289_flag "false"
-xref: spec_1_neutral_loss_1289_composition "O(3) S dHex Hex HexNAc(3) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1674
-name: dHex(1)Hex(3)HexA(1)HexNAc(2)Sulf(1)
-def: "DHex Hex(3) HexA HexNAc(2) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=3&hexa=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1674]
-xref: record_id "1674"
-xref: delta_mono_mass "1294.364027"
-xref: delta_avge_mass "1295.1354"
-xref: delta_composition "O(3) S dHex Hex(3) HexA HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:33:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1295_mono_mass "1294.364027"
-xref: spec_1_neutral_loss_1295_avge_mass "1295.1354"
-xref: spec_1_neutral_loss_1295_flag "false"
-xref: spec_1_neutral_loss_1295_composition "O(3) S dHex Hex(3) HexA HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1295_mono_mass "1294.364027"
-xref: spec_1_neutral_loss_1295_avge_mass "1295.1354"
-xref: spec_1_neutral_loss_1295_flag "false"
-xref: spec_1_neutral_loss_1295_composition "O(3) S dHex Hex(3) HexA HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1675
-name: dHex(1)Hex(1)HexNAc(2)NeuAc(2)
-def: "DHex Hex HexNAc(2) NeuAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=1&hexnac=2&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1675]
-xref: record_id "1675"
-xref: delta_mono_mass "1296.460311"
-xref: delta_avge_mass "1297.176"
-xref: delta_composition "dHex(1) Hex(1) HexNAc(2) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1297_mono_mass "1296.460311"
-xref: spec_1_neutral_loss_1297_avge_mass "1297.176"
-xref: spec_1_neutral_loss_1297_flag "false"
-xref: spec_1_neutral_loss_1297_composition "dHex(1) Hex(1) HexNAc(2) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1297_mono_mass "1296.460311"
-xref: spec_1_neutral_loss_1297_avge_mass "1297.176"
-xref: spec_1_neutral_loss_1297_flag "false"
-xref: spec_1_neutral_loss_1297_composition "dHex(1) Hex(1) HexNAc(2) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1676
-name: dHex(3)HexNAc(3)Kdn(1)
-def: "DHex(3) HexNAc(3) Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=3&hexnac=3&kdn=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1676]
-xref: record_id "1676"
-xref: delta_mono_mass "1297.480712"
-xref: delta_avge_mass "1298.2038"
-xref: delta_composition "dHex(3) HexNAc(3) Kdn"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 15:57:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1298_mono_mass "1297.480712"
-xref: spec_1_neutral_loss_1298_avge_mass "1298.2038"
-xref: spec_1_neutral_loss_1298_flag "false"
-xref: spec_1_neutral_loss_1298_composition "dHex(3) HexNAc(3) Kdn"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1298_mono_mass "1297.480712"
-xref: spec_1_neutral_loss_1298_avge_mass "1298.2038"
-xref: spec_1_neutral_loss_1298_flag "false"
-xref: spec_1_neutral_loss_1298_composition "dHex(3) HexNAc(3) Kdn"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1678
-name: Hex(2)HexNAc(3)NeuAc(1)Sulf(1)
-def: "Hex(2) HexNAc(3) NeuAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=2&hexnac=3&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1678]
-xref: record_id "1678"
-xref: delta_mono_mass "1304.395996"
-xref: delta_avge_mass "1305.1765"
-xref: delta_composition "O(3) S Hex(2) HexNAc(3) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:33:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1305_mono_mass "1304.395996"
-xref: spec_1_neutral_loss_1305_avge_mass "1305.1765"
-xref: spec_1_neutral_loss_1305_flag "false"
-xref: spec_1_neutral_loss_1305_composition "O(3) S Hex(2) HexNAc(3) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1305_mono_mass "1304.395996"
-xref: spec_1_neutral_loss_1305_avge_mass "1305.1765"
-xref: spec_1_neutral_loss_1305_flag "false"
-xref: spec_1_neutral_loss_1305_composition "O(3) S Hex(2) HexNAc(3) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1679
-name: dHex(2)Hex(2)HexNAc(3)Sulf(1)
-def: "DHex(2) Hex(2) HexNAc(3) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=2&hex=2&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1679]
-xref: record_id "1679"
-xref: delta_mono_mass "1305.416397"
-xref: delta_avge_mass "1306.2044"
-xref: delta_composition "O(3) S dHex(2) Hex(2) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:33:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1306_mono_mass "1305.416397"
-xref: spec_1_neutral_loss_1306_avge_mass "1306.2044"
-xref: spec_1_neutral_loss_1306_flag "false"
-xref: spec_1_neutral_loss_1306_composition "O(3) S dHex(2) Hex(2) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1306_mono_mass "1305.416397"
-xref: spec_1_neutral_loss_1306_avge_mass "1306.2044"
-xref: spec_1_neutral_loss_1306_flag "false"
-xref: spec_1_neutral_loss_1306_composition "O(3) S dHex(2) Hex(2) HexNAc(3)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1680
-name: dHex(2)HexNAc(5)
-def: "DHex(2) HexNAc(5)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1680]
-xref: record_id "1680"
-xref: delta_mono_mass "1307.512681"
-xref: delta_avge_mass "1308.245"
-xref: delta_composition "dHex(2) HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1308_mono_mass "1307.512681"
-xref: spec_1_neutral_loss_1308_avge_mass "1308.245"
-xref: spec_1_neutral_loss_1308_flag "false"
-xref: spec_1_neutral_loss_1308_composition "dHex(2) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1308_mono_mass "1307.512681"
-xref: spec_1_neutral_loss_1308_avge_mass "1308.245"
-xref: spec_1_neutral_loss_1308_flag "false"
-xref: spec_1_neutral_loss_1308_composition "dHex(2) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1681
-name: Hex(2)HexNAc(2)NeuAc(2)
-def: "Hex(2) HexNAc(2) NeuAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=2&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1681]
-xref: record_id "1681"
-xref: delta_mono_mass "1312.455225"
-xref: delta_avge_mass "1313.1754"
-xref: delta_composition "Hex(2) HexNAc(2) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1313_mono_mass "1312.455225"
-xref: spec_1_neutral_loss_1313_avge_mass "1313.1754"
-xref: spec_1_neutral_loss_1313_flag "false"
-xref: spec_1_neutral_loss_1313_composition "Hex(2) HexNAc(2) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1313_mono_mass "1312.455225"
-xref: spec_1_neutral_loss_1313_avge_mass "1313.1754"
-xref: spec_1_neutral_loss_1313_flag "false"
-xref: spec_1_neutral_loss_1313_composition "Hex(2) HexNAc(2) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1682
-name: dHex(2)Hex(2)HexNAc(2)NeuAc(1)
-def: "DHex(2) Hex(2) HexNAc(2) NeuAc ---OR--- Hex HexNAc(3) dHex(2) Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=2&hexnac=2&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1682]
-xref: record_id "1682"
-xref: delta_mono_mass "1313.475627"
-xref: delta_avge_mass "1314.2032"
-xref: delta_composition "dHex(2) Hex(2) HexNAc(2) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-17 13:21:07"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1314_mono_mass "1313.475627"
-xref: spec_1_neutral_loss_1314_avge_mass "1314.2032"
-xref: spec_1_neutral_loss_1314_flag "false"
-xref: spec_1_neutral_loss_1314_composition "dHex(2) Hex(2) HexNAc(2) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1314_mono_mass "1313.475627"
-xref: spec_1_neutral_loss_1314_avge_mass "1314.2032"
-xref: spec_1_neutral_loss_1314_flag "false"
-xref: spec_1_neutral_loss_1314_composition "dHex(2) Hex(2) HexNAc(2) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1683
-name: dHex(1)Hex(3)HexNAc(3)Sulf(1)
-def: "DHex Hex(3) HexNAc(3) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=3&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1683]
-xref: record_id "1683"
-xref: delta_mono_mass "1321.411312"
-xref: delta_avge_mass "1322.2038"
-xref: delta_composition "O(3) S dHex Hex(3) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:33:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1322_mono_mass "1321.411312"
-xref: spec_1_neutral_loss_1322_avge_mass "1322.2038"
-xref: spec_1_neutral_loss_1322_flag "false"
-xref: spec_1_neutral_loss_1322_composition "O(3) S dHex Hex(3) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1322_mono_mass "1321.411312"
-xref: spec_1_neutral_loss_1322_avge_mass "1322.2038"
-xref: spec_1_neutral_loss_1322_flag "false"
-xref: spec_1_neutral_loss_1322_composition "O(3) S dHex Hex(3) HexNAc(3)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1684
-name: dHex(2)Hex(2)HexNAc(2)NeuGc(1)
-def: "DHex(2) Hex(2) HexNAc(2) NeuGc ---OR--- Hex(3) HexNAc(2) dHex NeuAc ---OR--- Hex(2) HexNAc(3) dHex Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=2&hexnac=2&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1684]
-xref: record_id "1684"
-xref: delta_mono_mass "1329.470541"
-xref: delta_avge_mass "1330.2026"
-xref: delta_composition "dHex(2) Hex(2) HexNAc(2) NeuGc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-17 13:27:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1330_mono_mass "1329.470541"
-xref: spec_1_neutral_loss_1330_avge_mass "1330.2026"
-xref: spec_1_neutral_loss_1330_flag "false"
-xref: spec_1_neutral_loss_1330_composition "dHex(2) Hex(2) HexNAc(2) NeuGc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1330_mono_mass "1329.470541"
-xref: spec_1_neutral_loss_1330_avge_mass "1330.2026"
-xref: spec_1_neutral_loss_1330_flag "false"
-xref: spec_1_neutral_loss_1330_composition "dHex(2) Hex(2) HexNAc(2) NeuGc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1685
-name: Hex(2)HexNAc(5)
-def: "Hex(2) HexNAc(5)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1685]
-xref: record_id "1685"
-xref: delta_mono_mass "1339.50251"
-xref: delta_avge_mass "1340.2438"
-xref: delta_composition "Hex(2) HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1340_mono_mass "1339.50251"
-xref: spec_1_neutral_loss_1340_avge_mass "1340.2438"
-xref: spec_1_neutral_loss_1340_flag "false"
-xref: spec_1_neutral_loss_1340_composition "Hex(2) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1340_mono_mass "1339.50251"
-xref: spec_1_neutral_loss_1340_avge_mass "1340.2438"
-xref: spec_1_neutral_loss_1340_flag "false"
-xref: spec_1_neutral_loss_1340_composition "Hex(2) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1686
-name: dHex(1)Hex(3)HexNAc(2)NeuGc(1)
-def: "DHex Hex(3) HexNAc(2) NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexnac=2&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1686]
-xref: record_id "1686"
-xref: delta_mono_mass "1345.465456"
-xref: delta_avge_mass "1346.202"
-xref: delta_composition "dHex(1) Hex(3) HexNAc(2) NeuGc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1346_mono_mass "1345.465456"
-xref: spec_1_neutral_loss_1346_avge_mass "1346.202"
-xref: spec_1_neutral_loss_1346_flag "false"
-xref: spec_1_neutral_loss_1346_composition "dHex(1) Hex(3) HexNAc(2) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1346_mono_mass "1345.465456"
-xref: spec_1_neutral_loss_1346_avge_mass "1346.202"
-xref: spec_1_neutral_loss_1346_flag "false"
-xref: spec_1_neutral_loss_1346_composition "dHex(1) Hex(3) HexNAc(2) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1687
-name: Hex(1)HexNAc(3)NeuAc(2)
-def: "Hex HexNAc(3) NeuAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=3&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1687]
-xref: record_id "1687"
-xref: delta_mono_mass "1353.481775"
-xref: delta_avge_mass "1354.2273"
-xref: delta_composition "Hex(1) HexNAc(3) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1354_mono_mass "1353.481775"
-xref: spec_1_neutral_loss_1354_avge_mass "1354.2273"
-xref: spec_1_neutral_loss_1354_flag "false"
-xref: spec_1_neutral_loss_1354_composition "Hex(1) HexNAc(3) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1354_mono_mass "1353.481775"
-xref: spec_1_neutral_loss_1354_avge_mass "1354.2273"
-xref: spec_1_neutral_loss_1354_flag "false"
-xref: spec_1_neutral_loss_1354_composition "Hex(1) HexNAc(3) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1688
-name: dHex(1)Hex(2)HexNAc(3)NeuAc(1)
-def: "DHex Hex(2) HexNAc(3) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=2&hexnac=3&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1688]
-xref: record_id "1688"
-xref: delta_mono_mass "1370.49709"
-xref: delta_avge_mass "1371.2545"
-xref: delta_composition "dHex(1) Hex(2) HexNAc(3) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1371_mono_mass "1370.49709"
-xref: spec_1_neutral_loss_1371_avge_mass "1371.2545"
-xref: spec_1_neutral_loss_1371_flag "false"
-xref: spec_1_neutral_loss_1371_composition "dHex(1) Hex(2) HexNAc(3) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1371_mono_mass "1370.49709"
-xref: spec_1_neutral_loss_1371_avge_mass "1371.2545"
-xref: spec_1_neutral_loss_1371_flag "false"
-xref: spec_1_neutral_loss_1371_composition "dHex(1) Hex(2) HexNAc(3) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1689
-name: dHex(3)Hex(2)HexNAc(3)
-def: "DHex(3) Hex(2) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=3&hex=2&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1689]
-xref: record_id "1689"
-xref: delta_mono_mass "1371.517491"
-xref: delta_avge_mass "1372.2824"
-xref: delta_composition "dHex(3) Hex(2) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1372_mono_mass "1371.517491"
-xref: spec_1_neutral_loss_1372_avge_mass "1372.2824"
-xref: spec_1_neutral_loss_1372_flag "false"
-xref: spec_1_neutral_loss_1372_composition "dHex(3) Hex(2) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1372_mono_mass "1371.517491"
-xref: spec_1_neutral_loss_1372_avge_mass "1372.2824"
-xref: spec_1_neutral_loss_1372_flag "false"
-xref: spec_1_neutral_loss_1372_composition "dHex(3) Hex(2) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1690
-name: Hex(7)Phos(3)
-def: "Hex(7) Phos(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=3&hex=7&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1690]
-xref: record_id "1690"
-xref: delta_mono_mass "1374.268757"
-xref: delta_avge_mass "1374.9239"
-xref: delta_composition "H(3) O(9) P(3) Hex(7)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:43:14"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1375_mono_mass "1374.268757"
-xref: spec_1_neutral_loss_1375_avge_mass "1374.9239"
-xref: spec_1_neutral_loss_1375_flag "false"
-xref: spec_1_neutral_loss_1375_composition "H(3) O(9) P(3) Hex(7)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1375_mono_mass "1374.268757"
-xref: spec_1_neutral_loss_1375_avge_mass "1374.9239"
-xref: spec_1_neutral_loss_1375_flag "false"
-xref: spec_1_neutral_loss_1375_composition "H(3) O(9) P(3) Hex(7)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1691
-name: dHex(1)Hex(4)HexA(1)HexNAc(2)
-def: "DHex Hex(4) HexA HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=4&hexa=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1691]
-xref: record_id "1691"
-xref: delta_mono_mass "1376.460036"
-xref: delta_avge_mass "1377.2128"
-xref: delta_composition "dHex(1) Hex(4) HexA(1) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1377_mono_mass "1376.460036"
-xref: spec_1_neutral_loss_1377_avge_mass "1377.2128"
-xref: spec_1_neutral_loss_1377_flag "false"
-xref: spec_1_neutral_loss_1377_composition "dHex(1) Hex(4) HexA(1) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1377_mono_mass "1376.460036"
-xref: spec_1_neutral_loss_1377_avge_mass "1377.2128"
-xref: spec_1_neutral_loss_1377_flag "false"
-xref: spec_1_neutral_loss_1377_composition "dHex(1) Hex(4) HexA(1) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1692
-name: Hex(3)HexNAc(3)NeuAc(1)
-def: "Hex(3) HexNAc(3) NeuAc ---OR--- Hex(2) HexNAc(3) dHex NeuGc ---OR--- Hex(2) HexNAc(4) Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=3&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1692]
-xref: record_id "1692"
-xref: delta_mono_mass "1386.492005"
-xref: delta_avge_mass "1387.2539"
-xref: delta_composition "Hex(3) HexNAc(3) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-17 15:15:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1387_mono_mass "1386.492005"
-xref: spec_1_neutral_loss_1387_avge_mass "1387.2539"
-xref: spec_1_neutral_loss_1387_flag "false"
-xref: spec_1_neutral_loss_1387_composition "Hex(3) HexNAc(3) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1387_mono_mass "1386.492005"
-xref: spec_1_neutral_loss_1387_avge_mass "1387.2539"
-xref: spec_1_neutral_loss_1387_flag "false"
-xref: spec_1_neutral_loss_1387_composition "Hex(3) HexNAc(3) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1693
-name: dHex(1)Hex(3)HexA(2)HexNAc(2)
-def: "DHex Hex(3) HexA(2) HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexa=2&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1693]
-xref: record_id "1693"
-xref: delta_mono_mass "1390.439301"
-xref: delta_avge_mass "1391.1963"
-xref: delta_composition "dHex(1) Hex(3) HexA(2) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1391_mono_mass "1390.439301"
-xref: spec_1_neutral_loss_1391_avge_mass "1391.1963"
-xref: spec_1_neutral_loss_1391_flag "false"
-xref: spec_1_neutral_loss_1391_composition "dHex(1) Hex(3) HexA(2) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1391_mono_mass "1390.439301"
-xref: spec_1_neutral_loss_1391_avge_mass "1391.1963"
-xref: spec_1_neutral_loss_1391_flag "false"
-xref: spec_1_neutral_loss_1391_composition "dHex(1) Hex(3) HexA(2) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1694
-name: Hex(2)HexNAc(2)NeuAc(2)Sulf(1)
-def: "Hex(2) HexNAc(2) NeuAc(2) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=2&hexnac=2&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1694]
-xref: record_id "1694"
-xref: delta_mono_mass "1392.41204"
-xref: delta_avge_mass "1393.2386"
-xref: delta_composition "O(3) S Hex(2) HexNAc(2) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:34:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1393_mono_mass "1392.41204"
-xref: spec_1_neutral_loss_1393_avge_mass "1393.2386"
-xref: spec_1_neutral_loss_1393_flag "false"
-xref: spec_1_neutral_loss_1393_composition "O(3) S Hex(2) HexNAc(2) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1393_mono_mass "1392.41204"
-xref: spec_1_neutral_loss_1393_avge_mass "1393.2386"
-xref: spec_1_neutral_loss_1393_flag "false"
-xref: spec_1_neutral_loss_1393_composition "O(3) S Hex(2) HexNAc(2) NeuAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1695
-name: dHex(2)Hex(2)HexNAc(2)NeuAc(1)Sulf(1)
-def: "DHex(2) Hex(2) HexNAc(2) NeuAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=2&hex=2&hexnac=2&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1695]
-xref: record_id "1695"
-xref: delta_mono_mass "1393.432441"
-xref: delta_avge_mass "1394.2664"
-xref: delta_composition "O(3) S dHex(2) Hex(2) HexNAc(2) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:34:15"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1394_mono_mass "1393.432441"
-xref: spec_1_neutral_loss_1394_avge_mass "1394.2664"
-xref: spec_1_neutral_loss_1394_flag "false"
-xref: spec_1_neutral_loss_1394_composition "O(3) S dHex(2) Hex(2) HexNAc(2) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1394_mono_mass "1393.432441"
-xref: spec_1_neutral_loss_1394_avge_mass "1394.2664"
-xref: spec_1_neutral_loss_1394_flag "false"
-xref: spec_1_neutral_loss_1394_composition "O(3) S dHex(2) Hex(2) HexNAc(2) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1696
-name: Hex(3)HexNAc(3)NeuGc(1)
-def: "Hex(3) HexNAc(3) NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=3&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1696]
-xref: record_id "1696"
-xref: delta_mono_mass "1402.48692"
-xref: delta_avge_mass "1403.2533"
-xref: delta_composition "Hex(3) HexNAc(3) NeuGc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1403_mono_mass "1402.48692"
-xref: spec_1_neutral_loss_1403_avge_mass "1403.2533"
-xref: spec_1_neutral_loss_1403_flag "false"
-xref: spec_1_neutral_loss_1403_composition "Hex(3) HexNAc(3) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1403_mono_mass "1402.48692"
-xref: spec_1_neutral_loss_1403_avge_mass "1403.2533"
-xref: spec_1_neutral_loss_1403_flag "false"
-xref: spec_1_neutral_loss_1403_composition "Hex(3) HexNAc(3) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1697
-name: dHex(4)Hex(1)HexNAc(2)Kdn(1)
-def: "DHex(4) Hex HexNAc(2) Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=4&hex=1&hexnac=2&kdn=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1697]
-xref: record_id "1697"
-xref: delta_mono_mass "1402.512072"
-xref: delta_avge_mass "1403.2931"
-xref: delta_composition "dHex(4) Hex HexNAc(2) Kdn"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 15:56:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1403_mono_mass "1402.512072"
-xref: spec_1_neutral_loss_1403_avge_mass "1403.2931"
-xref: spec_1_neutral_loss_1403_flag "false"
-xref: spec_1_neutral_loss_1403_composition "dHex(4) Hex HexNAc(2) Kdn"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1403_mono_mass "1402.512072"
-xref: spec_1_neutral_loss_1403_avge_mass "1403.2931"
-xref: spec_1_neutral_loss_1403_flag "false"
-xref: spec_1_neutral_loss_1403_composition "dHex(4) Hex HexNAc(2) Kdn"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1698
-name: dHex(3)Hex(2)HexNAc(2)Kdn(1)
-def: "DHex(3) Hex(2) HexNAc(2) Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=3&hex=2&hexnac=2&kdn=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1698]
-xref: record_id "1698"
-xref: delta_mono_mass "1418.506986"
-xref: delta_avge_mass "1419.2925"
-xref: delta_composition "dHex(3) Hex(2) HexNAc(2) Kdn"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 15:56:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1419_mono_mass "1418.506986"
-xref: spec_1_neutral_loss_1419_avge_mass "1419.2925"
-xref: spec_1_neutral_loss_1419_flag "false"
-xref: spec_1_neutral_loss_1419_composition "dHex(3) Hex(2) HexNAc(2) Kdn"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1419_mono_mass "1418.506986"
-xref: spec_1_neutral_loss_1419_avge_mass "1419.2925"
-xref: spec_1_neutral_loss_1419_flag "false"
-xref: spec_1_neutral_loss_1419_composition "dHex(3) Hex(2) HexNAc(2) Kdn"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1699
-name: dHex(3)Hex(2)HexA(1)HexNAc(2)Sulf(1)
-def: "DHex(3) Hex(2) HexA HexNAc(2) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=3&hex=2&hexa=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1699]
-xref: record_id "1699"
-xref: delta_mono_mass "1424.427021"
-xref: delta_avge_mass "1425.2772"
-xref: delta_composition "O(3) S dHex(3) Hex(2) HexA HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:55:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1425_mono_mass "1424.427021"
-xref: spec_1_neutral_loss_1425_avge_mass "1425.2772"
-xref: spec_1_neutral_loss_1425_flag "false"
-xref: spec_1_neutral_loss_1425_composition "O(3) S dHex(3) Hex(2) HexA HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1425_mono_mass "1424.427021"
-xref: spec_1_neutral_loss_1425_avge_mass "1425.2772"
-xref: spec_1_neutral_loss_1425_flag "false"
-xref: spec_1_neutral_loss_1425_composition "O(3) S dHex(3) Hex(2) HexA HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1700
-name: Hex(2)HexNAc(4)NeuAc(1)
-def: "Hex(2) HexNAc(4) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=4&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1700]
-xref: record_id "1700"
-xref: delta_mono_mass "1427.518554"
-xref: delta_avge_mass "1428.3059"
-xref: delta_composition "Hex(2) HexNAc(4) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1428_mono_mass "1427.518554"
-xref: spec_1_neutral_loss_1428_avge_mass "1428.3059"
-xref: spec_1_neutral_loss_1428_flag "false"
-xref: spec_1_neutral_loss_1428_composition "Hex(2) HexNAc(4) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1428_mono_mass "1427.518554"
-xref: spec_1_neutral_loss_1428_avge_mass "1428.3059"
-xref: spec_1_neutral_loss_1428_flag "false"
-xref: spec_1_neutral_loss_1428_composition "Hex(2) HexNAc(4) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1701
-name: dHex(2)Hex(2)HexNAc(4)
-def: "DHex(2) Hex(2) HexNAc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=2&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1701]
-xref: record_id "1701"
-xref: delta_mono_mass "1428.538955"
-xref: delta_avge_mass "1429.3337"
-xref: delta_composition "dHex(2) Hex(2) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1429_mono_mass "1428.538955"
-xref: spec_1_neutral_loss_1429_avge_mass "1429.3337"
-xref: spec_1_neutral_loss_1429_flag "false"
-xref: spec_1_neutral_loss_1429_composition "dHex(2) Hex(2) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1429_mono_mass "1428.538955"
-xref: spec_1_neutral_loss_1429_avge_mass "1429.3337"
-xref: spec_1_neutral_loss_1429_flag "false"
-xref: spec_1_neutral_loss_1429_composition "dHex(2) Hex(2) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1702
-name: dHex(2)Hex(3)HexA(1)HexNAc(2)Sulf(1)
-def: "DHex(2) Hex(3) HexA HexNAc(2) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=2&hex=3&hexa=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1702]
-xref: record_id "1702"
-xref: delta_mono_mass "1440.421936"
-xref: delta_avge_mass "1441.2766"
-xref: delta_composition "O(3) S dHex(2) Hex(3) HexA HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:55:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1441_mono_mass "1440.421936"
-xref: spec_1_neutral_loss_1441_avge_mass "1441.2766"
-xref: spec_1_neutral_loss_1441_flag "false"
-xref: spec_1_neutral_loss_1441_composition "O(3) S dHex(2) Hex(3) HexA HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1441_mono_mass "1440.421936"
-xref: spec_1_neutral_loss_1441_avge_mass "1441.2766"
-xref: spec_1_neutral_loss_1441_flag "false"
-xref: spec_1_neutral_loss_1441_composition "O(3) S dHex(2) Hex(3) HexA HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1703
-name: dHex(4)HexNAc(3)Kdn(1)
-def: "DHex(4) HexNAc(3) Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=4&hexnac=3&kdn=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1703]
-xref: record_id "1703"
-xref: delta_mono_mass "1443.538621"
-xref: delta_avge_mass "1444.345"
-xref: delta_composition "dHex(4) HexNAc(3) Kdn"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 15:56:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1444_mono_mass "1443.538621"
-xref: spec_1_neutral_loss_1444_avge_mass "1444.345"
-xref: spec_1_neutral_loss_1444_flag "false"
-xref: spec_1_neutral_loss_1444_composition "dHex(4) HexNAc(3) Kdn"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1444_mono_mass "1443.538621"
-xref: spec_1_neutral_loss_1444_avge_mass "1444.345"
-xref: spec_1_neutral_loss_1444_flag "false"
-xref: spec_1_neutral_loss_1444_composition "dHex(4) HexNAc(3) Kdn"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1705
-name: Hex(2)HexNAc(1)NeuGc(3)
-def: "Hex(2) HexNAc NeuGc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=1&neugc=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1705]
-xref: record_id "1705"
-xref: delta_mono_mass "1448.456013"
-xref: delta_avge_mass "1449.2357"
-xref: delta_composition "Hex(2) HexNAc(1) NeuGc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1449_mono_mass "1448.456013"
-xref: spec_1_neutral_loss_1449_avge_mass "1449.2357"
-xref: spec_1_neutral_loss_1449_flag "false"
-xref: spec_1_neutral_loss_1449_composition "Hex(2) HexNAc(1) NeuGc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1449_mono_mass "1448.456013"
-xref: spec_1_neutral_loss_1449_avge_mass "1449.2357"
-xref: spec_1_neutral_loss_1449_flag "false"
-xref: spec_1_neutral_loss_1449_composition "Hex(2) HexNAc(1) NeuGc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1706
-name: dHex(4)Hex(1)HexNAc(1)Kdn(2)
-def: "DHex(4) Hex HexNAc Kdn(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=4&hex=1&hexnac=1&kdn=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1706]
-xref: record_id "1706"
-xref: delta_mono_mass "1449.501567"
-xref: delta_avge_mass "1450.3032"
-xref: delta_composition "dHex(4) Hex HexNAc Kdn(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 15:56:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1450_mono_mass "1449.501567"
-xref: spec_1_neutral_loss_1450_avge_mass "1450.3032"
-xref: spec_1_neutral_loss_1450_flag "false"
-xref: spec_1_neutral_loss_1450_composition "dHex(4) Hex HexNAc Kdn(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1450_mono_mass "1449.501567"
-xref: spec_1_neutral_loss_1450_avge_mass "1450.3032"
-xref: spec_1_neutral_loss_1450_flag "false"
-xref: spec_1_neutral_loss_1450_composition "dHex(4) Hex HexNAc Kdn(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1707
-name: dHex(1)Hex(2)HexNAc(3)NeuAc(1)Sulf(1)
-def: "DHex Hex(2) HexNAc(3) NeuAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=2&hexnac=3&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1707]
-xref: record_id "1707"
-xref: delta_mono_mass "1450.453905"
-xref: delta_avge_mass "1451.3177"
-xref: delta_composition "O(3) S dHex Hex(2) HexNAc(3) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:55:33"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1451_mono_mass "1450.453905"
-xref: spec_1_neutral_loss_1451_avge_mass "1451.3177"
-xref: spec_1_neutral_loss_1451_flag "false"
-xref: spec_1_neutral_loss_1451_composition "O(3) S dHex Hex(2) HexNAc(3) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1451_mono_mass "1450.453905"
-xref: spec_1_neutral_loss_1451_avge_mass "1451.3177"
-xref: spec_1_neutral_loss_1451_flag "false"
-xref: spec_1_neutral_loss_1451_composition "O(3) S dHex Hex(2) HexNAc(3) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1708
-name: dHex(1)Hex(2)HexNAc(2)NeuAc(2)
-def: "DHex Hex(2) HexNAc(2) NeuAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=2&hexnac=2&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1708]
-xref: record_id "1708"
-xref: delta_mono_mass "1458.513134"
-xref: delta_avge_mass "1459.3166"
-xref: delta_composition "dHex(1) Hex(2) HexNAc(2) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1459_mono_mass "1458.513134"
-xref: spec_1_neutral_loss_1459_avge_mass "1459.3166"
-xref: spec_1_neutral_loss_1459_flag "false"
-xref: spec_1_neutral_loss_1459_composition "dHex(1) Hex(2) HexNAc(2) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1459_mono_mass "1458.513134"
-xref: spec_1_neutral_loss_1459_avge_mass "1459.3166"
-xref: spec_1_neutral_loss_1459_flag "false"
-xref: spec_1_neutral_loss_1459_composition "dHex(1) Hex(2) HexNAc(2) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1709
-name: dHex(3)Hex(1)HexNAc(3)Kdn(1)
-def: "DHex(3) Hex HexNAc(3) Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=3&hex=1&hexnac=3&kdn=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1709]
-xref: record_id "1709"
-xref: delta_mono_mass "1459.533535"
-xref: delta_avge_mass "1460.3444"
-xref: delta_composition "dHex(3) Hex HexNAc(3) Kdn"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 15:56:20"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1460_mono_mass "1459.533535"
-xref: spec_1_neutral_loss_1460_avge_mass "1460.3444"
-xref: spec_1_neutral_loss_1460_flag "false"
-xref: spec_1_neutral_loss_1460_composition "dHex(3) Hex HexNAc(3) Kdn"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1460_mono_mass "1459.533535"
-xref: spec_1_neutral_loss_1460_avge_mass "1460.3444"
-xref: spec_1_neutral_loss_1460_flag "false"
-xref: spec_1_neutral_loss_1460_composition "dHex(3) Hex HexNAc(3) Kdn"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1711
-name: Hex(3)HexNAc(3)NeuAc(1)Sulf(1)
-def: "Hex(3) HexNAc(3) NeuAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=3&hexnac=3&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1711]
-xref: record_id "1711"
-xref: delta_mono_mass "1466.44882"
-xref: delta_avge_mass "1467.3171"
-xref: delta_composition "O(3) S Hex(3) HexNAc(3) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:55:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1467_mono_mass "1466.44882"
-xref: spec_1_neutral_loss_1467_avge_mass "1467.3171"
-xref: spec_1_neutral_loss_1467_flag "false"
-xref: spec_1_neutral_loss_1467_composition "O(3) S Hex(3) HexNAc(3) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1467_mono_mass "1466.44882"
-xref: spec_1_neutral_loss_1467_avge_mass "1467.3171"
-xref: spec_1_neutral_loss_1467_flag "false"
-xref: spec_1_neutral_loss_1467_composition "O(3) S Hex(3) HexNAc(3) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1712
-name: Hex(3)HexNAc(2)NeuAc(2)
-def: "Hex(3) HexNAc(2) NeuAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=2&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1712]
-xref: record_id "1712"
-xref: delta_mono_mass "1474.508049"
-xref: delta_avge_mass "1475.316"
-xref: delta_composition "Hex(3) HexNAc(2) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1475_mono_mass "1474.508049"
-xref: spec_1_neutral_loss_1475_avge_mass "1475.316"
-xref: spec_1_neutral_loss_1475_flag "false"
-xref: spec_1_neutral_loss_1475_composition "Hex(3) HexNAc(2) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1475_mono_mass "1474.508049"
-xref: spec_1_neutral_loss_1475_avge_mass "1475.316"
-xref: spec_1_neutral_loss_1475_flag "false"
-xref: spec_1_neutral_loss_1475_composition "Hex(3) HexNAc(2) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1713
-name: Hex(3)HexNAc(3)NeuGc(1)Sulf(1)
-def: "Hex(3) HexNAc(3) NeuGc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=3&hexnac=3&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1713]
-xref: record_id "1713"
-xref: delta_mono_mass "1482.443734"
-xref: delta_avge_mass "1483.3165"
-xref: delta_composition "O(3) S Hex(3) HexNAc(3) NeuGc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:55:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1483_mono_mass "1482.443734"
-xref: spec_1_neutral_loss_1483_avge_mass "1483.3165"
-xref: spec_1_neutral_loss_1483_flag "false"
-xref: spec_1_neutral_loss_1483_composition "O(3) S Hex(3) HexNAc(3) NeuGc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1483_mono_mass "1482.443734"
-xref: spec_1_neutral_loss_1483_avge_mass "1483.3165"
-xref: spec_1_neutral_loss_1483_flag "false"
-xref: spec_1_neutral_loss_1483_composition "O(3) S Hex(3) HexNAc(3) NeuGc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1714
-name: dHex(1)Hex(2)HexNAc(2)NeuGc(2)
-def: "DHex Hex(2) HexNAc(2) NeuGc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=2&hexnac=2&neugc=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1714]
-xref: record_id "1714"
-xref: delta_mono_mass "1490.502964"
-xref: delta_avge_mass "1491.3154"
-xref: delta_composition "dHex(1) Hex(2) HexNAc(2) NeuGc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1491_mono_mass "1490.502964"
-xref: spec_1_neutral_loss_1491_avge_mass "1491.3154"
-xref: spec_1_neutral_loss_1491_flag "false"
-xref: spec_1_neutral_loss_1491_composition "dHex(1) Hex(2) HexNAc(2) NeuGc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1491_mono_mass "1490.502964"
-xref: spec_1_neutral_loss_1491_avge_mass "1491.3154"
-xref: spec_1_neutral_loss_1491_flag "false"
-xref: spec_1_neutral_loss_1491_composition "dHex(1) Hex(2) HexNAc(2) NeuGc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1715
-name: dHex(2)Hex(3)HexNAc(2)NeuGc(1)
-def: "DHex(2) Hex(3) HexNAc(2) NeuGc ---OR--- Hex(4) HexNAc(2) dHex NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=3&hexnac=2&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1715]
-xref: record_id "1715"
-xref: delta_mono_mass "1491.523365"
-xref: delta_avge_mass "1492.3432"
-xref: delta_composition "dHex(2) Hex(3) HexNAc(2) NeuGc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-17 15:37:46"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1492_mono_mass "1491.523365"
-xref: spec_1_neutral_loss_1492_avge_mass "1492.3432"
-xref: spec_1_neutral_loss_1492_flag "false"
-xref: spec_1_neutral_loss_1492_composition "dHex(2) Hex(3) HexNAc(2) NeuGc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1492_mono_mass "1491.523365"
-xref: spec_1_neutral_loss_1492_avge_mass "1492.3432"
-xref: spec_1_neutral_loss_1492_flag "false"
-xref: spec_1_neutral_loss_1492_composition "dHex(2) Hex(3) HexNAc(2) NeuGc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1716
-name: dHex(1)Hex(3)HexA(1)HexNAc(3)Sulf(1)
-def: "DHex Hex(3) HexA HexNAc(3) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=3&hexa=1&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1716]
-xref: record_id "1716"
-xref: delta_mono_mass "1497.4434"
-xref: delta_avge_mass "1498.3279"
-xref: delta_composition "O(3) S dHex Hex(3) HexA HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:54:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1498_mono_mass "1497.4434"
-xref: spec_1_neutral_loss_1498_avge_mass "1498.3279"
-xref: spec_1_neutral_loss_1498_flag "false"
-xref: spec_1_neutral_loss_1498_composition "O(3) S dHex Hex(3) HexA HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1498_mono_mass "1497.4434"
-xref: spec_1_neutral_loss_1498_avge_mass "1498.3279"
-xref: spec_1_neutral_loss_1498_flag "false"
-xref: spec_1_neutral_loss_1498_composition "O(3) S dHex Hex(3) HexA HexNAc(3)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1717
-name: Hex(2)HexNAc(3)NeuAc(2)
-def: "Hex(2) HexNAc(3) NeuAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=3&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1717]
-xref: record_id "1717"
-xref: delta_mono_mass "1515.534598"
-xref: delta_avge_mass "1516.3679"
-xref: delta_composition "Hex(2) HexNAc(3) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1516_mono_mass "1515.534598"
-xref: spec_1_neutral_loss_1516_avge_mass "1516.3679"
-xref: spec_1_neutral_loss_1516_flag "false"
-xref: spec_1_neutral_loss_1516_composition "Hex(2) HexNAc(3) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1516_mono_mass "1515.534598"
-xref: spec_1_neutral_loss_1516_avge_mass "1516.3679"
-xref: spec_1_neutral_loss_1516_flag "false"
-xref: spec_1_neutral_loss_1516_composition "Hex(2) HexNAc(3) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1718
-name: dHex(2)Hex(2)HexNAc(3)NeuAc(1)
-def: "DHex(2) Hex(2) HexNAc(3) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=2&hexnac=3&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1718]
-xref: record_id "1718"
-xref: delta_mono_mass "1516.554999"
-xref: delta_avge_mass "1517.3957"
-xref: delta_composition "dHex(2) Hex(2) HexNAc(3) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1517_mono_mass "1516.554999"
-xref: spec_1_neutral_loss_1517_avge_mass "1517.3957"
-xref: spec_1_neutral_loss_1517_flag "false"
-xref: spec_1_neutral_loss_1517_composition "dHex(2) Hex(2) HexNAc(3) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1517_mono_mass "1516.554999"
-xref: spec_1_neutral_loss_1517_avge_mass "1517.3957"
-xref: spec_1_neutral_loss_1517_flag "false"
-xref: spec_1_neutral_loss_1517_composition "dHex(2) Hex(2) HexNAc(3) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1719
-name: dHex(4)Hex(2)HexNAc(3)
-def: "DHex(4) Hex(2) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=4&hex=2&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1719]
-xref: record_id "1719"
-xref: delta_mono_mass "1517.5754"
-xref: delta_avge_mass "1518.4236"
-xref: delta_composition "dHex(4) Hex(2) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1518_mono_mass "1517.5754"
-xref: spec_1_neutral_loss_1518_avge_mass "1518.4236"
-xref: spec_1_neutral_loss_1518_flag "false"
-xref: spec_1_neutral_loss_1518_composition "dHex(4) Hex(2) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1518_mono_mass "1517.5754"
-xref: spec_1_neutral_loss_1518_avge_mass "1518.4236"
-xref: spec_1_neutral_loss_1518_flag "false"
-xref: spec_1_neutral_loss_1518_composition "dHex(4) Hex(2) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1720
-name: Hex(2)HexNAc(3)NeuAc(1)NeuGc(1)
-def: "Hex(2) HexNAc(3) NeuAc NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=3&neuac=1&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1720]
-xref: record_id "1720"
-xref: delta_mono_mass "1531.529513"
-xref: delta_avge_mass "1532.3673"
-xref: delta_composition "Hex(2) HexNAc(3) NeuAc(1) NeuGc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1532_mono_mass "1531.529513"
-xref: spec_1_neutral_loss_1532_avge_mass "1532.3673"
-xref: spec_1_neutral_loss_1532_flag "false"
-xref: spec_1_neutral_loss_1532_composition "Hex(2) HexNAc(3) NeuAc(1) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1532_mono_mass "1531.529513"
-xref: spec_1_neutral_loss_1532_avge_mass "1532.3673"
-xref: spec_1_neutral_loss_1532_flag "false"
-xref: spec_1_neutral_loss_1532_composition "Hex(2) HexNAc(3) NeuAc(1) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1721
-name: dHex(2)Hex(2)HexNAc(3)NeuGc(1)
-def: "DHex(2) Hex(2) HexNAc(3) NeuGc ---OR--- Hex(3) HexNAc(3) dHex NeuAc ---OR--- Hex(2) HexNAc(4) dHex Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=2&hexnac=3&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1721]
-xref: record_id "1721"
-xref: delta_mono_mass "1532.549914"
-xref: delta_avge_mass "1533.3951"
-xref: delta_composition "dHex(2) Hex(2) HexNAc(3) NeuGc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-17 15:40:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1533_mono_mass "1532.549914"
-xref: spec_1_neutral_loss_1533_avge_mass "1533.3951"
-xref: spec_1_neutral_loss_1533_flag "false"
-xref: spec_1_neutral_loss_1533_composition "dHex(2) Hex(2) HexNAc(3) NeuGc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1533_mono_mass "1532.549914"
-xref: spec_1_neutral_loss_1533_avge_mass "1533.3951"
-xref: spec_1_neutral_loss_1533_flag "false"
-xref: spec_1_neutral_loss_1533_composition "dHex(2) Hex(2) HexNAc(3) NeuGc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1722
-name: dHex(3)Hex(3)HexNAc(3)
-def: "DHex(3) Hex(3) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=3&hex=3&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1722]
-xref: record_id "1722"
-xref: delta_mono_mass "1533.570315"
-xref: delta_avge_mass "1534.423"
-xref: delta_composition "dHex(3) Hex(3) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1534_mono_mass "1533.570315"
-xref: spec_1_neutral_loss_1534_avge_mass "1534.423"
-xref: spec_1_neutral_loss_1534_flag "false"
-xref: spec_1_neutral_loss_1534_composition "dHex(3) Hex(3) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1534_mono_mass "1533.570315"
-xref: spec_1_neutral_loss_1534_avge_mass "1534.423"
-xref: spec_1_neutral_loss_1534_flag "false"
-xref: spec_1_neutral_loss_1534_composition "dHex(3) Hex(3) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1723
-name: Hex(8)Phos(3)
-def: "Hex(8) Phos(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=3&hex=8&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1723]
-xref: record_id "1723"
-xref: delta_mono_mass "1536.321581"
-xref: delta_avge_mass "1537.0645"
-xref: delta_composition "H(3) O(9) P(3) Hex(8)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:43:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1537_mono_mass "1536.321581"
-xref: spec_1_neutral_loss_1537_avge_mass "1537.0645"
-xref: spec_1_neutral_loss_1537_flag "false"
-xref: spec_1_neutral_loss_1537_composition "H(3) O(9) P(3) Hex(8)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1537_mono_mass "1536.321581"
-xref: spec_1_neutral_loss_1537_avge_mass "1537.0645"
-xref: spec_1_neutral_loss_1537_flag "false"
-xref: spec_1_neutral_loss_1537_composition "H(3) O(9) P(3) Hex(8)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1724
-name: dHex(1)Hex(2)HexNAc(2)NeuAc(2)Sulf(1)
-def: "DHex Hex(2) HexNAc(2) NeuAc(2) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=2&hexnac=2&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1724]
-xref: record_id "1724"
-xref: delta_mono_mass "1538.469949"
-xref: delta_avge_mass "1539.3798"
-xref: delta_composition "O(3) S dHex Hex(2) HexNAc(2) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:54:39"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1539_mono_mass "1538.469949"
-xref: spec_1_neutral_loss_1539_avge_mass "1539.3798"
-xref: spec_1_neutral_loss_1539_flag "false"
-xref: spec_1_neutral_loss_1539_composition "O(3) S dHex Hex(2) HexNAc(2) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1539_mono_mass "1538.469949"
-xref: spec_1_neutral_loss_1539_avge_mass "1539.3798"
-xref: spec_1_neutral_loss_1539_flag "false"
-xref: spec_1_neutral_loss_1539_composition "O(3) S dHex Hex(2) HexNAc(2) NeuAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1725
-name: Hex(2)HexNAc(3)NeuGc(2)
-def: "Hex(2) HexNAc(3) NeuGc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=3&neugc=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1725]
-xref: record_id "1725"
-xref: delta_mono_mass "1547.524427"
-xref: delta_avge_mass "1548.3667"
-xref: delta_composition "Hex(2) HexNAc(3) NeuGc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1548_mono_mass "1547.524427"
-xref: spec_1_neutral_loss_1548_avge_mass "1548.3667"
-xref: spec_1_neutral_loss_1548_flag "false"
-xref: spec_1_neutral_loss_1548_composition "Hex(2) HexNAc(3) NeuGc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1548_mono_mass "1547.524427"
-xref: spec_1_neutral_loss_1548_avge_mass "1548.3667"
-xref: spec_1_neutral_loss_1548_flag "false"
-xref: spec_1_neutral_loss_1548_composition "Hex(2) HexNAc(3) NeuGc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1726
-name: dHex(4)Hex(2)HexNAc(2)Kdn(1)
-def: "DHex(4) Hex(2) HexNAc(2) Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=4&hex=2&hexnac=2&kdn=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1726]
-xref: record_id "1726"
-xref: delta_mono_mass "1564.564895"
-xref: delta_avge_mass "1565.4337"
-xref: delta_composition "dHex(4) Hex(2) HexNAc(2) Kdn"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 15:56:06"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1565_mono_mass "1564.564895"
-xref: spec_1_neutral_loss_1565_avge_mass "1565.4337"
-xref: spec_1_neutral_loss_1565_flag "false"
-xref: spec_1_neutral_loss_1565_composition "dHex(4) Hex(2) HexNAc(2) Kdn"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1565_mono_mass "1564.564895"
-xref: spec_1_neutral_loss_1565_avge_mass "1565.4337"
-xref: spec_1_neutral_loss_1565_flag "false"
-xref: spec_1_neutral_loss_1565_composition "dHex(4) Hex(2) HexNAc(2) Kdn"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1727
-name: dHex(1)Hex(2)HexNAc(4)NeuAc(1)
-def: "DHex Hex(2) HexNAc(4) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=2&hexnac=4&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1727]
-xref: record_id "1727"
-xref: delta_mono_mass "1573.576463"
-xref: delta_avge_mass "1574.4471"
-xref: delta_composition "dHex(1) Hex(2) HexNAc(4) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1574_mono_mass "1573.576463"
-xref: spec_1_neutral_loss_1574_avge_mass "1574.4471"
-xref: spec_1_neutral_loss_1574_flag "false"
-xref: spec_1_neutral_loss_1574_composition "dHex(1) Hex(2) HexNAc(4) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1574_mono_mass "1573.576463"
-xref: spec_1_neutral_loss_1574_avge_mass "1574.4471"
-xref: spec_1_neutral_loss_1574_flag "false"
-xref: spec_1_neutral_loss_1574_composition "dHex(1) Hex(2) HexNAc(4) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1728
-name: dHex(3)Hex(2)HexNAc(4)
-def: "DHex(3) Hex(2) HexNAc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=3&hex=2&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1728]
-xref: record_id "1728"
-xref: delta_mono_mass "1574.596864"
-xref: delta_avge_mass "1575.4749"
-xref: delta_composition "dHex(3) Hex(2) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1575_mono_mass "1574.596864"
-xref: spec_1_neutral_loss_1575_avge_mass "1575.4749"
-xref: spec_1_neutral_loss_1575_flag "false"
-xref: spec_1_neutral_loss_1575_composition "dHex(3) Hex(2) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1575_mono_mass "1574.596864"
-xref: spec_1_neutral_loss_1575_avge_mass "1575.4749"
-xref: spec_1_neutral_loss_1575_flag "false"
-xref: spec_1_neutral_loss_1575_composition "dHex(3) Hex(2) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1729
-name: Hex(1)HexNAc(1)NeuGc(4)
-def: "Hex HexNAc NeuGc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=1&neugc=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1729]
-xref: record_id "1729"
-xref: delta_mono_mass "1593.493521"
-xref: delta_avge_mass "1594.349"
-xref: delta_composition "Hex(1) HexNAc(1) NeuGc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1594_mono_mass "1593.493521"
-xref: spec_1_neutral_loss_1594_avge_mass "1594.349"
-xref: spec_1_neutral_loss_1594_flag "false"
-xref: spec_1_neutral_loss_1594_composition "Hex(1) HexNAc(1) NeuGc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1594_mono_mass "1593.493521"
-xref: spec_1_neutral_loss_1594_avge_mass "1594.349"
-xref: spec_1_neutral_loss_1594_flag "false"
-xref: spec_1_neutral_loss_1594_composition "Hex(1) HexNAc(1) NeuGc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1730
-name: dHex(4)Hex(1)HexNAc(3)Kdn(1)
-def: "DHex(4) Hex HexNAc(3) Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=4&hex=1&hexnac=3&kdn=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1730]
-xref: record_id "1730"
-xref: delta_mono_mass "1605.591444"
-xref: delta_avge_mass "1606.4856"
-xref: delta_composition "dHex(4) Hex HexNAc(3) Kdn"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 15:55:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1606_mono_mass "1605.591444"
-xref: spec_1_neutral_loss_1606_avge_mass "1606.4856"
-xref: spec_1_neutral_loss_1606_flag "false"
-xref: spec_1_neutral_loss_1606_composition "dHex(4) Hex HexNAc(3) Kdn"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1606_mono_mass "1605.591444"
-xref: spec_1_neutral_loss_1606_avge_mass "1606.4856"
-xref: spec_1_neutral_loss_1606_flag "false"
-xref: spec_1_neutral_loss_1606_composition "dHex(4) Hex HexNAc(3) Kdn"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1732
-name: Hex(4)HexNAc(4)Sulf(2)
-def: "Hex(4) HexNAc(4) Sulf(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=2&hex=4&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1732]
-xref: record_id "1732"
-xref: delta_mono_mass "1620.442414"
-xref: delta_avge_mass "1621.4589"
-xref: delta_composition "O(6) S(2) Hex(4) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:35:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1621_mono_mass "1620.442414"
-xref: spec_1_neutral_loss_1621_avge_mass "1621.4589"
-xref: spec_1_neutral_loss_1621_flag "false"
-xref: spec_1_neutral_loss_1621_composition "O(6) S(2) Hex(4) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1621_mono_mass "1620.442414"
-xref: spec_1_neutral_loss_1621_avge_mass "1621.4589"
-xref: spec_1_neutral_loss_1621_flag "false"
-xref: spec_1_neutral_loss_1621_composition "O(6) S(2) Hex(4) HexNAc(4)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1733
-name: dHex(3)Hex(2)HexNAc(3)Kdn(1)
-def: "DHex(3) Hex(2) HexNAc(3) Kdn ---OR--- Hex(3) HexNAc(2) dHex(3) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=3&hex=2&hexnac=3&kdn=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1733]
-xref: record_id "1733"
-xref: delta_mono_mass "1621.586359"
-xref: delta_avge_mass "1622.485"
-xref: delta_composition "dHex(3) Hex(2) HexNAc(3) Kdn"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-22 10:37:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1622_mono_mass "1621.586359"
-xref: spec_1_neutral_loss_1622_avge_mass "1622.485"
-xref: spec_1_neutral_loss_1622_flag "false"
-xref: spec_1_neutral_loss_1622_composition "dHex(3) Hex(2) HexNAc(3) Kdn"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1622_mono_mass "1621.586359"
-xref: spec_1_neutral_loss_1622_avge_mass "1622.485"
-xref: spec_1_neutral_loss_1622_flag "false"
-xref: spec_1_neutral_loss_1622_composition "dHex(3) Hex(2) HexNAc(3) Kdn"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1735
-name: dHex(2)Hex(2)HexNAc(5)
-def: "DHex(2) Hex(2) HexNAc(5)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=2&hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1735]
-xref: record_id "1735"
-xref: delta_mono_mass "1631.618328"
-xref: delta_avge_mass "1632.5262"
-xref: delta_composition "dHex(2) Hex(2) HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1632_mono_mass "1631.618328"
-xref: spec_1_neutral_loss_1632_avge_mass "1632.5262"
-xref: spec_1_neutral_loss_1632_flag "false"
-xref: spec_1_neutral_loss_1632_composition "dHex(2) Hex(2) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1632_mono_mass "1631.618328"
-xref: spec_1_neutral_loss_1632_avge_mass "1632.5262"
-xref: spec_1_neutral_loss_1632_flag "false"
-xref: spec_1_neutral_loss_1632_composition "dHex(2) Hex(2) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1736
-name: dHex(2)Hex(3)HexA(1)HexNAc(3)Sulf(1)
-def: "DHex(2) Hex(3) HexA HexNAc(3) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=2&hex=3&hexa=1&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1736]
-xref: record_id "1736"
-xref: delta_mono_mass "1643.501309"
-xref: delta_avge_mass "1644.4691"
-xref: delta_composition "O(3) S dHex(2) Hex(3) HexA HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:54:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1644_mono_mass "1643.501309"
-xref: spec_1_neutral_loss_1644_avge_mass "1644.4691"
-xref: spec_1_neutral_loss_1644_flag "false"
-xref: spec_1_neutral_loss_1644_composition "O(3) S dHex(2) Hex(3) HexA HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1644_mono_mass "1643.501309"
-xref: spec_1_neutral_loss_1644_avge_mass "1644.4691"
-xref: spec_1_neutral_loss_1644_flag "false"
-xref: spec_1_neutral_loss_1644_composition "O(3) S dHex(2) Hex(3) HexA HexNAc(3)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1737
-name: dHex(1)Hex(4)HexA(1)HexNAc(3)Sulf(1)
-def: "DHex Hex(4) HexA HexNAc(3) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=4&hexa=1&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1737]
-xref: record_id "1737"
-xref: delta_mono_mass "1659.496223"
-xref: delta_avge_mass "1660.4685"
-xref: delta_composition "O(3) S dHex Hex(4) HexA HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:54:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1660_mono_mass "1659.496223"
-xref: spec_1_neutral_loss_1660_avge_mass "1660.4685"
-xref: spec_1_neutral_loss_1660_flag "false"
-xref: spec_1_neutral_loss_1660_composition "O(3) S dHex Hex(4) HexA HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1660_mono_mass "1659.496223"
-xref: spec_1_neutral_loss_1660_avge_mass "1660.4685"
-xref: spec_1_neutral_loss_1660_flag "false"
-xref: spec_1_neutral_loss_1660_composition "O(3) S dHex Hex(4) HexA HexNAc(3)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1738
-name: Hex(3)HexNAc(3)NeuAc(2)
-def: "Hex(3) HexNAc(3) NeuAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=3&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1738]
-xref: record_id "1738"
-xref: delta_mono_mass "1677.587422"
-xref: delta_avge_mass "1678.5085"
-xref: delta_composition "Hex(3) HexNAc(3) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1678_mono_mass "1677.587422"
-xref: spec_1_neutral_loss_1678_avge_mass "1678.5085"
-xref: spec_1_neutral_loss_1678_flag "false"
-xref: spec_1_neutral_loss_1678_composition "Hex(3) HexNAc(3) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1678_mono_mass "1677.587422"
-xref: spec_1_neutral_loss_1678_avge_mass "1678.5085"
-xref: spec_1_neutral_loss_1678_flag "false"
-xref: spec_1_neutral_loss_1678_composition "Hex(3) HexNAc(3) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1739
-name: dHex(2)Hex(3)HexNAc(3)NeuAc(1)
-def: "DHex(2) Hex(3) HexNAc(3) NeuAc ---OR--- Hex(2) HexNAc(4) dHex(2) Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=3&hexnac=3&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1739]
-xref: record_id "1739"
-xref: delta_mono_mass "1678.607823"
-xref: delta_avge_mass "1679.5363"
-xref: delta_composition "dHex(2) Hex(3) HexNAc(3) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-22 10:51:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1679_mono_mass "1678.607823"
-xref: spec_1_neutral_loss_1679_avge_mass "1679.5363"
-xref: spec_1_neutral_loss_1679_flag "false"
-xref: spec_1_neutral_loss_1679_composition "dHex(2) Hex(3) HexNAc(3) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1679_mono_mass "1678.607823"
-xref: spec_1_neutral_loss_1679_avge_mass "1679.5363"
-xref: spec_1_neutral_loss_1679_flag "false"
-xref: spec_1_neutral_loss_1679_composition "dHex(2) Hex(3) HexNAc(3) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1740
-name: dHex(4)Hex(3)HexNAc(3)
-def: "DHex(4) Hex(3) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=4&hex=3&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1740]
-xref: record_id "1740"
-xref: delta_mono_mass "1679.628224"
-xref: delta_avge_mass "1680.5642"
-xref: delta_composition "dHex(4) Hex(3) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1680_mono_mass "1679.628224"
-xref: spec_1_neutral_loss_1680_avge_mass "1680.5642"
-xref: spec_1_neutral_loss_1680_flag "false"
-xref: spec_1_neutral_loss_1680_composition "dHex(4) Hex(3) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1680_mono_mass "1679.628224"
-xref: spec_1_neutral_loss_1680_avge_mass "1680.5642"
-xref: spec_1_neutral_loss_1680_flag "false"
-xref: spec_1_neutral_loss_1680_composition "dHex(4) Hex(3) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1742
-name: Hex(9)Phos(3)
-def: "Hex(9) Phos(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=3&hex=9&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1742]
-xref: record_id "1742"
-xref: delta_mono_mass "1698.374404"
-xref: delta_avge_mass "1699.2051"
-xref: delta_composition "H(3) O(9) P(3) Hex(9)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:47:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1699_mono_mass "1698.374404"
-xref: spec_1_neutral_loss_1699_avge_mass "1699.2051"
-xref: spec_1_neutral_loss_1699_flag "false"
-xref: spec_1_neutral_loss_1699_composition "H(3) O(9) P(3) Hex(9)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1699_mono_mass "1698.374404"
-xref: spec_1_neutral_loss_1699_avge_mass "1699.2051"
-xref: spec_1_neutral_loss_1699_flag "false"
-xref: spec_1_neutral_loss_1699_composition "H(3) O(9) P(3) Hex(9)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1743
-name: dHex(2)HexNAc(7)
-def: "DHex(2) HexNAc(7)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hexnac=7&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1743]
-xref: record_id "1743"
-xref: delta_mono_mass "1713.671426"
-xref: delta_avge_mass "1714.63"
-xref: delta_composition "dHex(2) HexNAc(7)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1714_mono_mass "1713.671426"
-xref: spec_1_neutral_loss_1714_avge_mass "1714.63"
-xref: spec_1_neutral_loss_1714_flag "false"
-xref: spec_1_neutral_loss_1714_composition "dHex(2) HexNAc(7)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1714_mono_mass "1713.671426"
-xref: spec_1_neutral_loss_1714_avge_mass "1714.63"
-xref: spec_1_neutral_loss_1714_flag "false"
-xref: spec_1_neutral_loss_1714_composition "dHex(2) HexNAc(7)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1744
-name: Hex(2)HexNAc(1)NeuGc(4)
-def: "Hex(2) HexNAc NeuGc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=1&neugc=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1744]
-xref: record_id "1744"
-xref: delta_mono_mass "1755.546345"
-xref: delta_avge_mass "1756.4896"
-xref: delta_composition "Hex(2) HexNAc(1) NeuGc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1756_mono_mass "1755.546345"
-xref: spec_1_neutral_loss_1756_avge_mass "1756.4896"
-xref: spec_1_neutral_loss_1756_flag "false"
-xref: spec_1_neutral_loss_1756_composition "Hex(2) HexNAc(1) NeuGc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1756_mono_mass "1755.546345"
-xref: spec_1_neutral_loss_1756_avge_mass "1756.4896"
-xref: spec_1_neutral_loss_1756_flag "false"
-xref: spec_1_neutral_loss_1756_composition "Hex(2) HexNAc(1) NeuGc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1745
-name: Hex(3)HexNAc(3)NeuAc(2)Sulf(1)
-def: "Hex(3) HexNAc(3) NeuAc(2) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=3&hexnac=3&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1745]
-xref: record_id "1745"
-xref: delta_mono_mass "1757.544236"
-xref: delta_avge_mass "1758.5717"
-xref: delta_composition "O(3) S Hex(3) HexNAc(3) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:54:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1758_mono_mass "1757.544236"
-xref: spec_1_neutral_loss_1758_avge_mass "1758.5717"
-xref: spec_1_neutral_loss_1758_flag "false"
-xref: spec_1_neutral_loss_1758_composition "O(3) S Hex(3) HexNAc(3) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1758_mono_mass "1757.544236"
-xref: spec_1_neutral_loss_1758_avge_mass "1758.5717"
-xref: spec_1_neutral_loss_1758_flag "false"
-xref: spec_1_neutral_loss_1758_composition "O(3) S Hex(3) HexNAc(3) NeuAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1746
-name: dHex(2)Hex(3)HexNAc(5)
-def: "DHex(2) Hex(3) HexNAc(5)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=3&hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1746]
-xref: record_id "1746"
-xref: delta_mono_mass "1793.671151"
-xref: delta_avge_mass "1794.6668"
-xref: delta_composition "dHex(2) Hex(3) HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-24 13:43:21"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1794_mono_mass "1793.671151"
-xref: spec_1_neutral_loss_1794_avge_mass "1794.6668"
-xref: spec_1_neutral_loss_1794_flag "false"
-xref: spec_1_neutral_loss_1794_composition "dHex(2) Hex(3) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1794_mono_mass "1793.671151"
-xref: spec_1_neutral_loss_1794_avge_mass "1794.6668"
-xref: spec_1_neutral_loss_1794_flag "false"
-xref: spec_1_neutral_loss_1794_composition "dHex(2) Hex(3) HexNAc(5)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1794_mono_mass "1793.671151"
-xref: spec_2_neutral_loss_1794_avge_mass "1794.6668"
-xref: spec_2_neutral_loss_1794_flag "false"
-xref: spec_2_neutral_loss_1794_composition "dHex(2) Hex(3) HexNAc(5)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1747
-name: dHex(1)Hex(2)HexNAc(2)NeuGc(3)
-def: "DHex Hex(2) HexNAc(2) NeuGc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=2&hexnac=2&neugc=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1747]
-xref: record_id "1747"
-xref: delta_mono_mass "1797.593295"
-xref: delta_avge_mass "1798.5694"
-xref: delta_composition "dHex(1) Hex(2) HexNAc(2) NeuGc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1798_mono_mass "1797.593295"
-xref: spec_1_neutral_loss_1798_avge_mass "1798.5694"
-xref: spec_1_neutral_loss_1798_flag "false"
-xref: spec_1_neutral_loss_1798_composition "dHex(1) Hex(2) HexNAc(2) NeuGc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1798_mono_mass "1797.593295"
-xref: spec_1_neutral_loss_1798_avge_mass "1798.5694"
-xref: spec_1_neutral_loss_1798_flag "false"
-xref: spec_1_neutral_loss_1798_composition "dHex(1) Hex(2) HexNAc(2) NeuGc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1748
-name: dHex(2)Hex(4)HexA(1)HexNAc(3)Sulf(1)
-def: "DHex(2) Hex(4) HexA HexNAc(3) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=2&hex=4&hexa=1&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1748]
-xref: record_id "1748"
-xref: delta_mono_mass "1805.554132"
-xref: delta_avge_mass "1806.6097"
-xref: delta_composition "O(3) S dHex(2) Hex(4) HexA HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:53:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1806_mono_mass "1805.554132"
-xref: spec_1_neutral_loss_1806_avge_mass "1806.6097"
-xref: spec_1_neutral_loss_1806_flag "false"
-xref: spec_1_neutral_loss_1806_composition "O(3) S dHex(2) Hex(4) HexA HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1806_mono_mass "1805.554132"
-xref: spec_1_neutral_loss_1806_avge_mass "1806.6097"
-xref: spec_1_neutral_loss_1806_flag "false"
-xref: spec_1_neutral_loss_1806_composition "O(3) S dHex(2) Hex(4) HexA HexNAc(3)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1749
-name: Hex(2)HexNAc(3)NeuAc(3)
-def: "Hex(2) HexNAc(3) NeuAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=3&neuac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1749]
-xref: record_id "1749"
-xref: delta_mono_mass "1806.630015"
-xref: delta_avge_mass "1807.6225"
-xref: delta_composition "Hex(2) HexNAc(3) NeuAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1807_mono_mass "1806.630015"
-xref: spec_1_neutral_loss_1807_avge_mass "1807.6225"
-xref: spec_1_neutral_loss_1807_flag "false"
-xref: spec_1_neutral_loss_1807_composition "Hex(2) HexNAc(3) NeuAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1807_mono_mass "1806.630015"
-xref: spec_1_neutral_loss_1807_avge_mass "1807.6225"
-xref: spec_1_neutral_loss_1807_flag "false"
-xref: spec_1_neutral_loss_1807_composition "Hex(2) HexNAc(3) NeuAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1750
-name: dHex(1)Hex(3)HexNAc(3)NeuAc(2)
-def: "DHex Hex(3) HexNAc(3) NeuAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexnac=3&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1750]
-xref: record_id "1750"
-xref: delta_mono_mass "1823.64533"
-xref: delta_avge_mass "1824.6497"
-xref: delta_composition "dHex(1) Hex(3) HexNAc(3) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1824_mono_mass "1823.64533"
-xref: spec_1_neutral_loss_1824_avge_mass "1824.6497"
-xref: spec_1_neutral_loss_1824_flag "false"
-xref: spec_1_neutral_loss_1824_composition "dHex(1) Hex(3) HexNAc(3) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1824_mono_mass "1823.64533"
-xref: spec_1_neutral_loss_1824_avge_mass "1824.6497"
-xref: spec_1_neutral_loss_1824_flag "false"
-xref: spec_1_neutral_loss_1824_composition "dHex(1) Hex(3) HexNAc(3) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1751
-name: dHex(3)Hex(3)HexNAc(3)NeuAc(1)
-def: "DHex(3) Hex(3) HexNAc(3) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=3&hex=3&hexnac=3&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1751]
-xref: record_id "1751"
-xref: delta_mono_mass "1824.665732"
-xref: delta_avge_mass "1825.6775"
-xref: delta_composition "dHex(3) Hex(3) HexNAc(3) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1825_mono_mass "1824.665732"
-xref: spec_1_neutral_loss_1825_avge_mass "1825.6775"
-xref: spec_1_neutral_loss_1825_flag "false"
-xref: spec_1_neutral_loss_1825_composition "dHex(3) Hex(3) HexNAc(3) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1825_mono_mass "1824.665732"
-xref: spec_1_neutral_loss_1825_avge_mass "1825.6775"
-xref: spec_1_neutral_loss_1825_flag "false"
-xref: spec_1_neutral_loss_1825_composition "dHex(3) Hex(3) HexNAc(3) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1752
-name: Hex(2)HexNAc(3)NeuGc(3)
-def: "Hex(2) HexNAc(3) NeuGc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=3&neugc=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1752]
-xref: record_id "1752"
-xref: delta_mono_mass "1854.614759"
-xref: delta_avge_mass "1855.6207"
-xref: delta_composition "Hex(2) HexNAc(3) NeuGc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1855_mono_mass "1854.614759"
-xref: spec_1_neutral_loss_1855_avge_mass "1855.6207"
-xref: spec_1_neutral_loss_1855_flag "false"
-xref: spec_1_neutral_loss_1855_composition "Hex(2) HexNAc(3) NeuGc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1855_mono_mass "1854.614759"
-xref: spec_1_neutral_loss_1855_avge_mass "1855.6207"
-xref: spec_1_neutral_loss_1855_flag "false"
-xref: spec_1_neutral_loss_1855_composition "Hex(2) HexNAc(3) NeuGc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1753
-name: Hex(10)Phos(3)
-def: "Hex(10) Phos(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=3&hex=10&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1753]
-xref: record_id "1753"
-xref: delta_mono_mass "1860.427228"
-xref: delta_avge_mass "1861.3457"
-xref: delta_composition "H(3) O(9) P(3) Hex(10)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:51:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1861_mono_mass "1860.427228"
-xref: spec_1_neutral_loss_1861_avge_mass "1861.3457"
-xref: spec_1_neutral_loss_1861_flag "false"
-xref: spec_1_neutral_loss_1861_composition "H(3) O(9) P(3) Hex(10)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1861_mono_mass "1860.427228"
-xref: spec_1_neutral_loss_1861_avge_mass "1861.3457"
-xref: spec_1_neutral_loss_1861_flag "false"
-xref: spec_1_neutral_loss_1861_composition "H(3) O(9) P(3) Hex(10)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1754
-name: dHex(1)Hex(2)HexNAc(4)NeuAc(2)
-def: "DHex Hex(2) HexNAc(4) NeuAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=2&hexnac=4&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1754]
-xref: record_id "1754"
-xref: delta_mono_mass "1864.67188"
-xref: delta_avge_mass "1865.7016"
-xref: delta_composition "dHex(1) Hex(2) HexNAc(4) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1865_mono_mass "1864.67188"
-xref: spec_1_neutral_loss_1865_avge_mass "1865.7016"
-xref: spec_1_neutral_loss_1865_flag "false"
-xref: spec_1_neutral_loss_1865_composition "dHex(1) Hex(2) HexNAc(4) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1865_mono_mass "1864.67188"
-xref: spec_1_neutral_loss_1865_avge_mass "1865.7016"
-xref: spec_1_neutral_loss_1865_flag "false"
-xref: spec_1_neutral_loss_1865_composition "dHex(1) Hex(2) HexNAc(4) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1755
-name: Hex(1)HexNAc(1)NeuGc(5)
-def: "Hex HexNAc NeuGc(5)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=1&neugc=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1755]
-xref: record_id "1755"
-xref: delta_mono_mass "1900.583852"
-xref: delta_avge_mass "1901.603"
-xref: delta_composition "Hex(1) HexNAc(1) NeuGc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1901_mono_mass "1900.583852"
-xref: spec_1_neutral_loss_1901_avge_mass "1901.603"
-xref: spec_1_neutral_loss_1901_flag "false"
-xref: spec_1_neutral_loss_1901_composition "Hex(1) HexNAc(1) NeuGc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1901_mono_mass "1900.583852"
-xref: spec_1_neutral_loss_1901_avge_mass "1901.603"
-xref: spec_1_neutral_loss_1901_flag "false"
-xref: spec_1_neutral_loss_1901_composition "Hex(1) HexNAc(1) NeuGc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1756
-name: Hex(4)HexNAc(4)NeuAc(1)Sulf(2)
-def: "Hex(4) HexNAc(4) NeuAc Sulf(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=2&hex=4&hexnac=4&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1756]
-xref: record_id "1756"
-xref: delta_mono_mass "1911.53783"
-xref: delta_avge_mass "1912.7135"
-xref: delta_composition "O(6) S(2) Hex(4) HexNAc(4) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:50:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1912_mono_mass "1911.53783"
-xref: spec_1_neutral_loss_1912_avge_mass "1912.7135"
-xref: spec_1_neutral_loss_1912_flag "false"
-xref: spec_1_neutral_loss_1912_composition "O(6) S(2) Hex(4) HexNAc(4) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1912_mono_mass "1911.53783"
-xref: spec_1_neutral_loss_1912_avge_mass "1912.7135"
-xref: spec_1_neutral_loss_1912_flag "false"
-xref: spec_1_neutral_loss_1912_composition "O(6) S(2) Hex(4) HexNAc(4) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1757
-name: Hex(4)HexNAc(4)NeuGc(1)Sulf(2)
-def: "Hex(4) HexNAc(4) NeuGc Sulf(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=2&hex=4&hexnac=4&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1757]
-xref: record_id "1757"
-xref: delta_mono_mass "1927.532745"
-xref: delta_avge_mass "1928.7129"
-xref: delta_composition "O(6) S(2) Hex(4) HexNAc(4) NeuGc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:50:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1928_mono_mass "1927.532745"
-xref: spec_1_neutral_loss_1928_avge_mass "1928.7129"
-xref: spec_1_neutral_loss_1928_flag "false"
-xref: spec_1_neutral_loss_1928_composition "O(6) S(2) Hex(4) HexNAc(4) NeuGc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1928_mono_mass "1927.532745"
-xref: spec_1_neutral_loss_1928_avge_mass "1928.7129"
-xref: spec_1_neutral_loss_1928_flag "false"
-xref: spec_1_neutral_loss_1928_composition "O(6) S(2) Hex(4) HexNAc(4) NeuGc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1758
-name: dHex(2)Hex(3)HexNAc(3)NeuAc(2)
-def: "DHex(2) Hex(3) HexNAc(3) NeuAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=3&hexnac=3&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1758]
-xref: record_id "1758"
-xref: delta_mono_mass "1969.703239"
-xref: delta_avge_mass "1970.7909"
-xref: delta_composition "dHex(2) Hex(3) HexNAc(3) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1970_mono_mass "1969.703239"
-xref: spec_1_neutral_loss_1970_avge_mass "1970.7909"
-xref: spec_1_neutral_loss_1970_flag "false"
-xref: spec_1_neutral_loss_1970_composition "dHex(2) Hex(3) HexNAc(3) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1970_mono_mass "1969.703239"
-xref: spec_1_neutral_loss_1970_avge_mass "1970.7909"
-xref: spec_1_neutral_loss_1970_flag "false"
-xref: spec_1_neutral_loss_1970_composition "dHex(2) Hex(3) HexNAc(3) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1759
-name: Hex(4)HexNAc(4)NeuAc(1)Sulf(3)
-def: "Hex(4) HexNAc(4) NeuAc Sulf(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=3&hex=4&hexnac=4&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1759]
-xref: record_id "1759"
-xref: delta_mono_mass "1991.494645"
-xref: delta_avge_mass "1992.7767"
-xref: delta_composition "O(9) S(3) Hex(4) HexNAc(4) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:50:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1992_mono_mass "1991.494645"
-xref: spec_1_neutral_loss_1992_avge_mass "1992.7767"
-xref: spec_1_neutral_loss_1992_flag "false"
-xref: spec_1_neutral_loss_1992_composition "O(9) S(3) Hex(4) HexNAc(4) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1992_mono_mass "1991.494645"
-xref: spec_1_neutral_loss_1992_avge_mass "1992.7767"
-xref: spec_1_neutral_loss_1992_flag "false"
-xref: spec_1_neutral_loss_1992_composition "O(9) S(3) Hex(4) HexNAc(4) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1760
-name: dHex(2)Hex(2)HexNAc(2)
-def: "DHex(2) Hex(2) HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=2&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1760]
-xref: record_id "1760"
-xref: delta_mono_mass "1022.38021"
-xref: delta_avge_mass "1022.9486"
-xref: delta_composition "dHex(2) Hex(2) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1023_mono_mass "1022.38021"
-xref: spec_1_neutral_loss_1023_avge_mass "1022.9486"
-xref: spec_1_neutral_loss_1023_flag "false"
-xref: spec_1_neutral_loss_1023_composition "dHex(2) Hex(2) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1023_mono_mass "1022.38021"
-xref: spec_1_neutral_loss_1023_avge_mass "1022.9486"
-xref: spec_1_neutral_loss_1023_flag "false"
-xref: spec_1_neutral_loss_1023_composition "dHex(2) Hex(2) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1023_mono_mass "1022.38021"
-xref: spec_2_neutral_loss_1023_avge_mass "1022.9486"
-xref: spec_2_neutral_loss_1023_flag "false"
-xref: spec_2_neutral_loss_1023_composition "dHex(2) Hex(2) HexNAc(2)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1761
-name: dHex(1)Hex(3)HexNAc(2)
-def: "DHex Hex(3) HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1761]
-xref: record_id "1761"
-xref: delta_mono_mass "1038.375125"
-xref: delta_avge_mass "1038.948"
-xref: delta_composition "dHex(1) Hex(3) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1039_mono_mass "1038.375125"
-xref: spec_1_neutral_loss_1039_avge_mass "1038.948"
-xref: spec_1_neutral_loss_1039_flag "false"
-xref: spec_1_neutral_loss_1039_composition "dHex(1) Hex(3) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1039_mono_mass "1038.375125"
-xref: spec_1_neutral_loss_1039_avge_mass "1038.948"
-xref: spec_1_neutral_loss_1039_flag "false"
-xref: spec_1_neutral_loss_1039_composition "dHex(1) Hex(3) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1039_mono_mass "1038.375125"
-xref: spec_2_neutral_loss_1039_avge_mass "1038.948"
-xref: spec_2_neutral_loss_1039_flag "false"
-xref: spec_2_neutral_loss_1039_composition "dHex(1) Hex(3) HexNAc(2)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1762
-name: dHex(1)Hex(2)HexNAc(3)
-def: "DHex Hex(2) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=2&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1762]
-xref: record_id "1762"
-xref: delta_mono_mass "1079.401674"
-xref: delta_avge_mass "1080"
-xref: delta_composition "dHex(1) Hex(2) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1080_mono_mass "1079.401674"
-xref: spec_1_neutral_loss_1080_avge_mass "1080"
-xref: spec_1_neutral_loss_1080_flag "false"
-xref: spec_1_neutral_loss_1080_composition "dHex(1) Hex(2) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1080_mono_mass "1079.401674"
-xref: spec_1_neutral_loss_1080_avge_mass "1080"
-xref: spec_1_neutral_loss_1080_flag "false"
-xref: spec_1_neutral_loss_1080_composition "dHex(1) Hex(2) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1080_mono_mass "1079.401674"
-xref: spec_2_neutral_loss_1080_avge_mass "1080"
-xref: spec_2_neutral_loss_1080_flag "false"
-xref: spec_2_neutral_loss_1080_composition "dHex(1) Hex(2) HexNAc(3)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1763
-name: Hex(3)HexNAc(3)
-def: "Hex(3) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1763]
-xref: record_id "1763"
-xref: delta_mono_mass "1095.396588"
-xref: delta_avge_mass "1095.9994"
-xref: delta_composition "Hex(3) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1096_mono_mass "1095.396588"
-xref: spec_1_neutral_loss_1096_avge_mass "1095.9994"
-xref: spec_1_neutral_loss_1096_flag "false"
-xref: spec_1_neutral_loss_1096_composition "Hex(3) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1096_mono_mass "1095.396588"
-xref: spec_1_neutral_loss_1096_avge_mass "1095.9994"
-xref: spec_1_neutral_loss_1096_flag "false"
-xref: spec_1_neutral_loss_1096_composition "Hex(3) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1096_mono_mass "1095.396588"
-xref: spec_2_neutral_loss_1096_avge_mass "1095.9994"
-xref: spec_2_neutral_loss_1096_flag "false"
-xref: spec_2_neutral_loss_1096_composition "Hex(3) HexNAc(3)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1764
-name: dHex(1)Hex(3)HexNAc(2)Sulf(1)
-def: "DHex Hex(3) HexNAc(2) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=3&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1764]
-xref: record_id "1764"
-xref: delta_mono_mass "1118.331939"
-xref: delta_avge_mass "1119.0112"
-xref: delta_composition "O(3) S dHex Hex(3) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:49:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1119_mono_mass "1118.331939"
-xref: spec_1_neutral_loss_1119_avge_mass "1119.0112"
-xref: spec_1_neutral_loss_1119_flag "false"
-xref: spec_1_neutral_loss_1119_composition "O(3) S dHex Hex(3) HexNAc(2)"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1119_mono_mass "1118.331939"
-xref: spec_1_neutral_loss_1119_avge_mass "1119.0112"
-xref: spec_1_neutral_loss_1119_flag "false"
-xref: spec_1_neutral_loss_1119_composition "O(3) S dHex Hex(3) HexNAc(2)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1119_mono_mass "1118.331939"
-xref: spec_2_neutral_loss_1119_avge_mass "1119.0112"
-xref: spec_2_neutral_loss_1119_flag "false"
-xref: spec_2_neutral_loss_1119_composition "O(3) S dHex Hex(3) HexNAc(2)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1765
-name: dHex(2)Hex(3)HexNAc(2)
-def: "DHex(2) Hex(3) HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=3&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1765]
-xref: record_id "1765"
-xref: delta_mono_mass "1184.433033"
-xref: delta_avge_mass "1185.0892"
-xref: delta_composition "dHex(2) Hex(3) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1185_mono_mass "1184.433033"
-xref: spec_1_neutral_loss_1185_avge_mass "1185.0892"
-xref: spec_1_neutral_loss_1185_flag "false"
-xref: spec_1_neutral_loss_1185_composition "dHex(2) Hex(3) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1185_mono_mass "1184.433033"
-xref: spec_1_neutral_loss_1185_avge_mass "1185.0892"
-xref: spec_1_neutral_loss_1185_flag "false"
-xref: spec_1_neutral_loss_1185_composition "dHex(2) Hex(3) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1185_mono_mass "1184.433033"
-xref: spec_2_neutral_loss_1185_avge_mass "1185.0892"
-xref: spec_2_neutral_loss_1185_flag "false"
-xref: spec_2_neutral_loss_1185_composition "dHex(2) Hex(3) HexNAc(2)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1766
-name: dHex(1)Hex(4)HexNAc(2)
-def: "DHex Hex(4) HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hexac=2&mode=exact, URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=4&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1766]
-xref: record_id "1766"
-xref: delta_mono_mass "1200.427948"
-xref: delta_avge_mass "1201.0886"
-xref: delta_composition "dHex(1) Hex(4) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1201_mono_mass "1200.427948"
-xref: spec_1_neutral_loss_1201_avge_mass "1201.0886"
-xref: spec_1_neutral_loss_1201_flag "false"
-xref: spec_1_neutral_loss_1201_composition "dHex(1) Hex(4) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1201_mono_mass "1200.427948"
-xref: spec_1_neutral_loss_1201_avge_mass "1201.0886"
-xref: spec_1_neutral_loss_1201_flag "false"
-xref: spec_1_neutral_loss_1201_composition "dHex(1) Hex(4) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1201_mono_mass "1200.427948"
-xref: spec_2_neutral_loss_1201_avge_mass "1201.0886"
-xref: spec_2_neutral_loss_1201_flag "false"
-xref: spec_2_neutral_loss_1201_composition "dHex(1) Hex(4) HexNAc(2)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1767
-name: dHex(2)Hex(2)HexNAc(3)
-def: "DHex(2) Hex(2) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=2&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1767]
-xref: record_id "1767"
-xref: delta_mono_mass "1225.459583"
-xref: delta_avge_mass "1226.1412"
-xref: delta_composition "dHex(2) Hex(2) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1226_mono_mass "1225.459583"
-xref: spec_1_neutral_loss_1226_avge_mass "1226.1412"
-xref: spec_1_neutral_loss_1226_flag "false"
-xref: spec_1_neutral_loss_1226_composition "dHex(2) Hex(2) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1226_mono_mass "1225.459583"
-xref: spec_1_neutral_loss_1226_avge_mass "1226.1412"
-xref: spec_1_neutral_loss_1226_flag "false"
-xref: spec_1_neutral_loss_1226_composition "dHex(2) Hex(2) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1226_mono_mass "1225.459583"
-xref: spec_2_neutral_loss_1226_avge_mass "1226.1412"
-xref: spec_2_neutral_loss_1226_flag "false"
-xref: spec_2_neutral_loss_1226_composition "dHex(2) Hex(2) HexNAc(3)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1768
-name: dHex(1)Hex(3)HexNAc(3)
-def: "DHex Hex(3) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1768]
-xref: record_id "1768"
-xref: delta_mono_mass "1241.454497"
-xref: delta_avge_mass "1242.1406"
-xref: delta_composition "dHex(1) Hex(3) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1242_mono_mass "1241.454497"
-xref: spec_1_neutral_loss_1242_avge_mass "1242.1406"
-xref: spec_1_neutral_loss_1242_flag "false"
-xref: spec_1_neutral_loss_1242_composition "dHex(1) Hex(3) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1242_mono_mass "1241.454497"
-xref: spec_1_neutral_loss_1242_avge_mass "1242.1406"
-xref: spec_1_neutral_loss_1242_flag "false"
-xref: spec_1_neutral_loss_1242_composition "dHex(1) Hex(3) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1242_mono_mass "1241.454497"
-xref: spec_2_neutral_loss_1242_avge_mass "1242.1406"
-xref: spec_2_neutral_loss_1242_flag "false"
-xref: spec_2_neutral_loss_1242_composition "dHex(1) Hex(3) HexNAc(3)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1769
-name: Hex(4)HexNAc(3)
-def: "Hex(4) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1769]
-xref: record_id "1769"
-xref: delta_mono_mass "1257.449412"
-xref: delta_avge_mass "1258.14"
-xref: delta_composition "Hex(4) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1258_mono_mass "1257.449412"
-xref: spec_1_neutral_loss_1258_avge_mass "1258.14"
-xref: spec_1_neutral_loss_1258_flag "false"
-xref: spec_1_neutral_loss_1258_composition "Hex(4) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1258_mono_mass "1257.449412"
-xref: spec_1_neutral_loss_1258_avge_mass "1258.14"
-xref: spec_1_neutral_loss_1258_flag "false"
-xref: spec_1_neutral_loss_1258_composition "Hex(4) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1258_mono_mass "1257.449412"
-xref: spec_2_neutral_loss_1258_avge_mass "1258.14"
-xref: spec_2_neutral_loss_1258_flag "false"
-xref: spec_2_neutral_loss_1258_composition "Hex(4) HexNAc(3)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1770
-name: dHex(2)Hex(4)HexNAc(2)
-def: "DHex(2) Hex(4) HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=4&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1770]
-xref: record_id "1770"
-xref: delta_mono_mass "1346.485857"
-xref: delta_avge_mass "1347.2298"
-xref: delta_composition "dHex(2) Hex(4) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1347_mono_mass "1346.485857"
-xref: spec_1_neutral_loss_1347_avge_mass "1347.2298"
-xref: spec_1_neutral_loss_1347_flag "false"
-xref: spec_1_neutral_loss_1347_composition "dHex(2) Hex(4) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1347_mono_mass "1346.485857"
-xref: spec_1_neutral_loss_1347_avge_mass "1347.2298"
-xref: spec_1_neutral_loss_1347_flag "false"
-xref: spec_1_neutral_loss_1347_composition "dHex(2) Hex(4) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1347_mono_mass "1346.485857"
-xref: spec_2_neutral_loss_1347_avge_mass "1347.2298"
-xref: spec_2_neutral_loss_1347_flag "false"
-xref: spec_2_neutral_loss_1347_composition "dHex(2) Hex(4) HexNAc(2)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1771
-name: dHex(2)Hex(3)HexNAc(3)
-def: "DHex(2) Hex(3) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=3&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1771]
-xref: record_id "1771"
-xref: delta_mono_mass "1387.512406"
-xref: delta_avge_mass "1388.2818"
-xref: delta_composition "dHex(2) Hex(3) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1388_mono_mass "1387.512406"
-xref: spec_1_neutral_loss_1388_avge_mass "1388.2818"
-xref: spec_1_neutral_loss_1388_flag "false"
-xref: spec_1_neutral_loss_1388_composition "dHex(2) Hex(3) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1388_mono_mass "1387.512406"
-xref: spec_1_neutral_loss_1388_avge_mass "1388.2818"
-xref: spec_1_neutral_loss_1388_flag "false"
-xref: spec_1_neutral_loss_1388_composition "dHex(2) Hex(3) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1388_mono_mass "1387.512406"
-xref: spec_2_neutral_loss_1388_avge_mass "1388.2818"
-xref: spec_2_neutral_loss_1388_flag "false"
-xref: spec_2_neutral_loss_1388_composition "dHex(2) Hex(3) HexNAc(3)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1772
-name: Hex(3)HexNAc(5)
-def: "A3." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1772]
-xref: record_id "1772"
-xref: delta_mono_mass "1501.555334"
-xref: delta_avge_mass "1502.3844"
-xref: delta_composition "Hex(3) HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2020-08-02 11:46:20"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1502_mono_mass "1501.555334"
-xref: spec_1_neutral_loss_1502_avge_mass "1502.3844"
-xref: spec_1_neutral_loss_1502_flag "false"
-xref: spec_1_neutral_loss_1502_composition "Hex(3) HexNAc(5)"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1502_mono_mass "1501.555334"
-xref: spec_1_neutral_loss_1502_avge_mass "1502.3844"
-xref: spec_1_neutral_loss_1502_flag "false"
-xref: spec_1_neutral_loss_1502_composition "Hex(3) HexNAc(5)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1502_mono_mass "1501.555334"
-xref: spec_2_neutral_loss_1502_avge_mass "1502.3844"
-xref: spec_2_neutral_loss_1502_flag "false"
-xref: spec_2_neutral_loss_1502_composition "Hex(3) HexNAc(5)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1773
-name: Hex(4)HexNAc(3)NeuAc(1)
-def: "Hex(4) HexNAc(3) NeuAc ---OR--- Hex(3) HexNAc(4) Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexnac=3&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1773]
-xref: record_id "1773"
-xref: delta_mono_mass "1548.544828"
-xref: delta_avge_mass "1549.3945"
-xref: delta_composition "Hex(4) HexNAc(3) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-17 15:42:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1549_mono_mass "1548.544828"
-xref: spec_1_neutral_loss_1549_avge_mass "1549.3945"
-xref: spec_1_neutral_loss_1549_flag "false"
-xref: spec_1_neutral_loss_1549_composition "Hex(4) HexNAc(3) NeuAc"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1549_mono_mass "1548.544828"
-xref: spec_1_neutral_loss_1549_avge_mass "1549.3945"
-xref: spec_1_neutral_loss_1549_flag "false"
-xref: spec_1_neutral_loss_1549_composition "Hex(4) HexNAc(3) NeuAc"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1549_mono_mass "1548.544828"
-xref: spec_2_neutral_loss_1549_avge_mass "1549.3945"
-xref: spec_2_neutral_loss_1549_flag "false"
-xref: spec_2_neutral_loss_1549_composition "Hex(4) HexNAc(3) NeuAc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1774
-name: dHex(2)Hex(3)HexNAc(4)
-def: "DHex(2) Hex(3) HexNAc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=3&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1774]
-xref: record_id "1774"
-xref: delta_mono_mass "1590.591779"
-xref: delta_avge_mass "1591.4743"
-xref: delta_composition "dHex(2) Hex(3) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1591_mono_mass "1590.591779"
-xref: spec_1_neutral_loss_1591_avge_mass "1591.4743"
-xref: spec_1_neutral_loss_1591_flag "false"
-xref: spec_1_neutral_loss_1591_composition "dHex(2) Hex(3) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1591_mono_mass "1590.591779"
-xref: spec_1_neutral_loss_1591_avge_mass "1591.4743"
-xref: spec_1_neutral_loss_1591_flag "false"
-xref: spec_1_neutral_loss_1591_composition "dHex(2) Hex(3) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1591_mono_mass "1590.591779"
-xref: spec_2_neutral_loss_1591_avge_mass "1591.4743"
-xref: spec_2_neutral_loss_1591_flag "false"
-xref: spec_2_neutral_loss_1591_composition "dHex(2) Hex(3) HexNAc(4)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1775
-name: dHex(1)Hex(3)HexNAc(5)
-def: "DHex Hex(3) HexNAc(5)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1775]
-xref: record_id "1775"
-xref: delta_mono_mass "1647.613242"
-xref: delta_avge_mass "1648.5256"
-xref: delta_composition "dHex(1) Hex(3) HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1648_mono_mass "1647.613242"
-xref: spec_1_neutral_loss_1648_avge_mass "1648.5256"
-xref: spec_1_neutral_loss_1648_flag "false"
-xref: spec_1_neutral_loss_1648_composition "dHex(1) Hex(3) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1648_mono_mass "1647.613242"
-xref: spec_1_neutral_loss_1648_avge_mass "1648.5256"
-xref: spec_1_neutral_loss_1648_flag "false"
-xref: spec_1_neutral_loss_1648_composition "dHex(1) Hex(3) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1648_mono_mass "1647.613242"
-xref: spec_2_neutral_loss_1648_avge_mass "1648.5256"
-xref: spec_2_neutral_loss_1648_flag "false"
-xref: spec_2_neutral_loss_1648_composition "dHex(1) Hex(3) HexNAc(5)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1776
-name: Hex(3)HexNAc(6)
-def: "A4." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=6&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1776]
-xref: record_id "1776"
-xref: delta_mono_mass "1704.634706"
-xref: delta_avge_mass "1705.5769"
-xref: delta_composition "Hex(3) HexNAc(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2020-08-02 11:48:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1705_mono_mass "1704.634706"
-xref: spec_1_neutral_loss_1705_avge_mass "1705.5769"
-xref: spec_1_neutral_loss_1705_flag "false"
-xref: spec_1_neutral_loss_1705_composition "Hex(3) HexNAc(6)"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1705_mono_mass "1704.634706"
-xref: spec_1_neutral_loss_1705_avge_mass "1705.5769"
-xref: spec_1_neutral_loss_1705_flag "false"
-xref: spec_1_neutral_loss_1705_composition "Hex(3) HexNAc(6)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1705_mono_mass "1704.634706"
-xref: spec_2_neutral_loss_1705_avge_mass "1705.5769"
-xref: spec_2_neutral_loss_1705_flag "false"
-xref: spec_2_neutral_loss_1705_composition "Hex(3) HexNAc(6)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1777
-name: Hex(4)HexNAc(4)NeuAc(1)
-def: "Hex(4) HexNAc(4) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexnac=4&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1777]
-xref: record_id "1777"
-xref: delta_mono_mass "1751.624201"
-xref: delta_avge_mass "1752.5871"
-xref: delta_composition "Hex(4) HexNAc(4) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1752_mono_mass "1751.624201"
-xref: spec_1_neutral_loss_1752_avge_mass "1752.5871"
-xref: spec_1_neutral_loss_1752_flag "false"
-xref: spec_1_neutral_loss_1752_composition "Hex(4) HexNAc(4) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1752_mono_mass "1751.624201"
-xref: spec_1_neutral_loss_1752_avge_mass "1752.5871"
-xref: spec_1_neutral_loss_1752_flag "false"
-xref: spec_1_neutral_loss_1752_composition "Hex(4) HexNAc(4) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1752_mono_mass "1751.624201"
-xref: spec_2_neutral_loss_1752_avge_mass "1752.5871"
-xref: spec_2_neutral_loss_1752_flag "false"
-xref: spec_2_neutral_loss_1752_composition "Hex(4) HexNAc(4) NeuAc(1)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1778
-name: dHex(2)Hex(4)HexNAc(4)
-def: "DHex(2) Hex(4) HexNAc(4) ---OR--- Hex(4) HexNAc(4) dHex Pent Me." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=4&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1778]
-xref: record_id "1778"
-xref: delta_mono_mass "1752.644602"
-xref: delta_avge_mass "1753.6149"
-xref: delta_composition "dHex(2) Hex(4) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-22 11:07:26"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1753_mono_mass "1752.644602"
-xref: spec_1_neutral_loss_1753_avge_mass "1753.6149"
-xref: spec_1_neutral_loss_1753_flag "false"
-xref: spec_1_neutral_loss_1753_composition "dHex(2) Hex(4) HexNAc(4)"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1753_mono_mass "1752.644602"
-xref: spec_1_neutral_loss_1753_avge_mass "1753.6149"
-xref: spec_1_neutral_loss_1753_flag "false"
-xref: spec_1_neutral_loss_1753_composition "dHex(2) Hex(4) HexNAc(4)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_1753_mono_mass "1752.644602"
-xref: spec_2_neutral_loss_1753_avge_mass "1753.6149"
-xref: spec_2_neutral_loss_1753_flag "false"
-xref: spec_2_neutral_loss_1753_composition "dHex(2) Hex(4) HexNAc(4)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1779
-name: Hex(6)HexNAc(4)
-def: "Hex(6) HexNAc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=6&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1779]
-xref: record_id "1779"
-xref: delta_mono_mass "1784.634431"
-xref: delta_avge_mass "1785.6137"
-xref: delta_composition "Hex(6) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1785_mono_mass "1784.634431"
-xref: spec_1_neutral_loss_1785_avge_mass "1785.6137"
-xref: spec_1_neutral_loss_1785_flag "false"
-xref: spec_1_neutral_loss_1785_composition "Hex(6) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1785_mono_mass "1784.634431"
-xref: spec_1_neutral_loss_1785_avge_mass "1785.6137"
-xref: spec_1_neutral_loss_1785_flag "false"
-xref: spec_1_neutral_loss_1785_composition "Hex(6) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1785_mono_mass "1784.634431"
-xref: spec_2_neutral_loss_1785_avge_mass "1785.6137"
-xref: spec_2_neutral_loss_1785_flag "false"
-xref: spec_2_neutral_loss_1785_composition "Hex(6) HexNAc(4)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1780
-name: Hex(5)HexNAc(5)
-def: "Hex(5) HexNAc(5)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=5&hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1780]
-xref: record_id "1780"
-xref: delta_mono_mass "1825.660981"
-xref: delta_avge_mass "1826.6656"
-xref: delta_composition "Hex(5) HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1826_mono_mass "1825.660981"
-xref: spec_1_neutral_loss_1826_avge_mass "1826.6656"
-xref: spec_1_neutral_loss_1826_flag "false"
-xref: spec_1_neutral_loss_1826_composition "Hex(5) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1826_mono_mass "1825.660981"
-xref: spec_1_neutral_loss_1826_avge_mass "1826.6656"
-xref: spec_1_neutral_loss_1826_flag "false"
-xref: spec_1_neutral_loss_1826_composition "Hex(5) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1826_mono_mass "1825.660981"
-xref: spec_2_neutral_loss_1826_avge_mass "1826.6656"
-xref: spec_2_neutral_loss_1826_flag "false"
-xref: spec_2_neutral_loss_1826_composition "Hex(5) HexNAc(5)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1781
-name: dHex(1)Hex(3)HexNAc(6)
-def: "DHex Hex(3) HexNAc(6)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexnac=6&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1781]
-xref: record_id "1781"
-xref: delta_mono_mass "1850.692615"
-xref: delta_avge_mass "1851.7181"
-xref: delta_composition "dHex(1) Hex(3) HexNAc(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1851_mono_mass "1850.692615"
-xref: spec_1_neutral_loss_1851_avge_mass "1851.7181"
-xref: spec_1_neutral_loss_1851_flag "false"
-xref: spec_1_neutral_loss_1851_composition "dHex(1) Hex(3) HexNAc(6)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1851_mono_mass "1850.692615"
-xref: spec_1_neutral_loss_1851_avge_mass "1851.7181"
-xref: spec_1_neutral_loss_1851_flag "false"
-xref: spec_1_neutral_loss_1851_composition "dHex(1) Hex(3) HexNAc(6)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1851_mono_mass "1850.692615"
-xref: spec_2_neutral_loss_1851_avge_mass "1851.7181"
-xref: spec_2_neutral_loss_1851_flag "false"
-xref: spec_2_neutral_loss_1851_composition "dHex(1) Hex(3) HexNAc(6)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1782
-name: dHex(1)Hex(4)HexNAc(4)NeuAc(1)
-def: "DHex Hex(4) HexNAc(4) NeuAc ---OR--- Hex(3) HexNAc(5) dHex Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=4&hexnac=4&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1782]
-xref: record_id "1782"
-xref: delta_mono_mass "1897.68211"
-xref: delta_avge_mass "1898.7283"
-xref: delta_composition "dHex Hex(4) HexNAc(4) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-22 11:17:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1898_mono_mass "1897.68211"
-xref: spec_1_neutral_loss_1898_avge_mass "1898.7283"
-xref: spec_1_neutral_loss_1898_flag "false"
-xref: spec_1_neutral_loss_1898_composition "dHex Hex(4) HexNAc(4) NeuAc"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1898_mono_mass "1897.68211"
-xref: spec_1_neutral_loss_1898_avge_mass "1898.7283"
-xref: spec_1_neutral_loss_1898_flag "false"
-xref: spec_1_neutral_loss_1898_composition "dHex Hex(4) HexNAc(4) NeuAc"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_1898_mono_mass "1897.68211"
-xref: spec_2_neutral_loss_1898_avge_mass "1898.7283"
-xref: spec_2_neutral_loss_1898_flag "false"
-xref: spec_2_neutral_loss_1898_composition "dHex Hex(4) HexNAc(4) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1783
-name: dHex(3)Hex(4)HexNAc(4)
-def: "DHex(3) Hex(4) HexNAc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=3&hex=4&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1783]
-xref: record_id "1783"
-xref: delta_mono_mass "1898.702511"
-xref: delta_avge_mass "1899.7561"
-xref: delta_composition "dHex(3) Hex(4) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1899_mono_mass "1898.702511"
-xref: spec_1_neutral_loss_1899_avge_mass "1899.7561"
-xref: spec_1_neutral_loss_1899_flag "false"
-xref: spec_1_neutral_loss_1899_composition "dHex(3) Hex(4) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1899_mono_mass "1898.702511"
-xref: spec_1_neutral_loss_1899_avge_mass "1899.7561"
-xref: spec_1_neutral_loss_1899_flag "false"
-xref: spec_1_neutral_loss_1899_composition "dHex(3) Hex(4) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1899_mono_mass "1898.702511"
-xref: spec_2_neutral_loss_1899_avge_mass "1899.7561"
-xref: spec_2_neutral_loss_1899_flag "false"
-xref: spec_2_neutral_loss_1899_composition "dHex(3) Hex(4) HexNAc(4)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1784
-name: dHex(1)Hex(3)HexNAc(5)NeuAc(1)
-def: "DHex Hex(3) HexNAc(5) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexnac=5&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1784]
-xref: record_id "1784"
-xref: delta_mono_mass "1938.708659"
-xref: delta_avge_mass "1939.7802"
-xref: delta_composition "dHex(1) Hex(3) HexNAc(5) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1939_mono_mass "1938.708659"
-xref: spec_1_neutral_loss_1939_avge_mass "1939.7802"
-xref: spec_1_neutral_loss_1939_flag "false"
-xref: spec_1_neutral_loss_1939_composition "dHex(1) Hex(3) HexNAc(5) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1939_mono_mass "1938.708659"
-xref: spec_1_neutral_loss_1939_avge_mass "1939.7802"
-xref: spec_1_neutral_loss_1939_flag "false"
-xref: spec_1_neutral_loss_1939_composition "dHex(1) Hex(3) HexNAc(5) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1939_mono_mass "1938.708659"
-xref: spec_2_neutral_loss_1939_avge_mass "1939.7802"
-xref: spec_2_neutral_loss_1939_flag "false"
-xref: spec_2_neutral_loss_1939_composition "dHex(1) Hex(3) HexNAc(5) NeuAc(1)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1785
-name: dHex(2)Hex(4)HexNAc(5)
-def: "DHex(2) Hex(4) HexNAc(5)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=4&hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1785]
-xref: record_id "1785"
-xref: delta_mono_mass "1955.723975"
-xref: delta_avge_mass "1956.8074"
-xref: delta_composition "dHex(2) Hex(4) HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1956_mono_mass "1955.723975"
-xref: spec_1_neutral_loss_1956_avge_mass "1956.8074"
-xref: spec_1_neutral_loss_1956_flag "false"
-xref: spec_1_neutral_loss_1956_composition "dHex(2) Hex(4) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1956_mono_mass "1955.723975"
-xref: spec_1_neutral_loss_1956_avge_mass "1956.8074"
-xref: spec_1_neutral_loss_1956_flag "false"
-xref: spec_1_neutral_loss_1956_composition "dHex(2) Hex(4) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1956_mono_mass "1955.723975"
-xref: spec_2_neutral_loss_1956_avge_mass "1956.8074"
-xref: spec_2_neutral_loss_1956_flag "false"
-xref: spec_2_neutral_loss_1956_composition "dHex(2) Hex(4) HexNAc(5)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1786
-name: Hex(1)HexNAc(1)NeuAc(1)Ac(1)
-def: "Ac Hex HexNAc NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?acetyl=1&hex=1&hexnac=1&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1786]
-xref: record_id "1786"
-xref: delta_mono_mass "698.238177"
-xref: delta_avge_mass "698.6244"
-xref: delta_composition "Ac Hex HexNAc NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 16:37:35"
-xref: date_time_modified "2015-05-06 09:37:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_699_mono_mass "698.238177"
-xref: spec_1_neutral_loss_699_avge_mass "698.6244"
-xref: spec_1_neutral_loss_699_flag "false"
-xref: spec_1_neutral_loss_699_composition "Ac Hex HexNAc NeuAc"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_699_mono_mass "698.238177"
-xref: spec_1_neutral_loss_699_avge_mass "698.6244"
-xref: spec_1_neutral_loss_699_flag "false"
-xref: spec_1_neutral_loss_699_composition "Ac Hex HexNAc NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1787
-name: Label:13C(2)15N(2)
-def: "13C(2) 15N(2)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1787]
-comment: For SILAC experiments.
-synonym: "K4" RELATED []
-xref: record_id "1787"
-xref: delta_mono_mass "4.00078"
-xref: delta_avge_mass "3.9721"
-xref: delta_composition "C(-2) 13C(2) N(-2) 15N(2)"
-xref: username_of_poster "rbomgard"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-15 22:30:48"
-xref: date_time_modified "2015-05-24 18:09:48"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1789
-name: Xlink:DSS[155]
-def: "Ammonium-quenched monolink of DSS/BS3 crosslinker." [PMID:8326953, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1789]
-xref: record_id "1789"
-xref: delta_mono_mass "155.094629"
-xref: delta_avge_mass "155.1943"
-xref: delta_composition "H(13) C(8) N O(2)"
-xref: username_of_poster "johant"
-xref: group_of_poster ""
-xref: date_time_posted "2015-06-17 14:35:50"
-xref: date_time_modified "2017-08-17 15:09:42"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1799
-name: NQIGG
-def: "SUMOylation by Giardia lamblia." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1799]
-xref: record_id "1799"
-xref: delta_mono_mass "469.228496"
-xref: delta_avge_mass "469.4921"
-xref: delta_composition "H(31) C(19) N(7) O(7)"
-xref: username_of_poster "brunog"
-xref: group_of_poster ""
-xref: date_time_posted "2015-10-02 16:16:32"
-xref: date_time_modified "2015-11-01 16:20:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1800
-name: Carboxyethylpyrrole
-def: "Carboxyethylpyrrole." [PMID:12923198, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1800]
-xref: record_id "1800"
-xref: delta_mono_mass "122.036779"
-xref: delta_avge_mass "122.1213"
-xref: delta_composition "H(6) C(7) O(2)"
-xref: username_of_poster "jsc17"
-xref: group_of_poster ""
-xref: date_time_posted "2015-11-19 01:35:22"
-xref: date_time_modified "2016-04-06 08:03:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1801
-name: Fluorescein-tyramine
-def: "Fluorescein-tyramine adduct by peroxidase activity." [URL:http\://www.biosyn.com/tew/tyramide-signal-amplification.aspx, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1801]
-xref: record_id "1801"
-xref: delta_mono_mass "493.116152"
-xref: delta_avge_mass "493.4637"
-xref: delta_composition "H(19) C(29) N O(7)"
-xref: username_of_poster "Hideaki"
-xref: group_of_poster ""
-xref: date_time_posted "2016-02-02 11:23:24"
-xref: date_time_modified "2016-04-06 08:08:06"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1824
-name: GEE
-def: "Transamidation of glycine ethyl ester to glutamine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1824]
-xref: record_id "1824"
-xref: delta_mono_mass "86.036779"
-xref: delta_avge_mass "86.0892"
-xref: delta_composition "H(6) C(4) O(2)"
-xref: username_of_poster "michaelmerchant"
-xref: group_of_poster ""
-xref: date_time_posted "2016-05-12 15:56:17"
-xref: date_time_modified "2016-05-18 17:11:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "GEE (glycine ethyl ester) is a substrate for the enzyme Factor XIII for cross-linking to fibrinogen"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1825
-name: RNPXL
-def: "Simulate peptide-RNA conjugates." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1825]
-xref: record_id "1825"
-xref: delta_mono_mass "324.035867"
-xref: delta_avge_mass "324.1813"
-xref: delta_composition "H(13) C(9) N(2) O(9) P"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2016-06-05 14:23:58"
-xref: date_time_modified "2016-07-01 11:23:46"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Other"
-xref: spec_1_neutral_loss_325_mono_mass "324.035867"
-xref: spec_1_neutral_loss_325_avge_mass "324.1813"
-xref: spec_1_neutral_loss_325_flag "false"
-xref: spec_1_neutral_loss_325_composition "H(13) C(9) N(2) O(9) P"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "R"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Other"
-xref: spec_2_neutral_loss_325_mono_mass "324.035867"
-xref: spec_2_neutral_loss_325_avge_mass "324.1813"
-xref: spec_2_neutral_loss_325_flag "false"
-xref: spec_2_neutral_loss_325_composition "H(13) C(9) N(2) O(9) P"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1826
-name: Glu->pyro-Glu+Methyl
-def: "Pyro-Glu from E + Methylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1826]
-xref: record_id "1826"
-xref: delta_mono_mass "-3.994915"
-xref: delta_avge_mass "-3.9887"
-xref: delta_composition "C O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2016-06-15 10:07:50"
-xref: date_time_modified "2016-06-15 10:07:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1827
-name: Glu->pyro-Glu+Methyl:2H(2)13C(1)
-def: "Pyro-Glu from E + Methylation Medium." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1827]
-xref: record_id "1827"
-xref: delta_mono_mass "-0.979006"
-xref: delta_avge_mass "-0.9837"
-xref: delta_composition "H(-2) 2H(2) 13C O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2016-06-15 10:30:37"
-xref: date_time_modified "2016-06-15 10:30:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1828
-name: LRGG+methyl
-def: "LeumethylArgGlyGly." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1828]
-comment: LRGG remnant of ubiquitin remaining attached to lysine with missed cleavage due to methylation of arginine.
-synonym: "LRGG ubiquitin remnant with methylated Arg" RELATED []
-xref: record_id "1828"
-xref: delta_mono_mass "397.243753"
-xref: delta_avge_mass "397.4725"
-xref: delta_composition "H(31) C(17) N(7) O(4)"
-xref: username_of_poster "bkatja"
-xref: group_of_poster ""
-xref: date_time_posted "2016-07-27 14:34:54"
-xref: date_time_modified "2016-09-23 13:43:32"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1829
-name: LRGG+dimethyl
-def: "LeudimethylArgGlyGly." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1829]
-comment: LRGG remnant of ubiquitin remaining attached to lysine with missed cleavage due to dimethylation of arginine.
-synonym: "LRGG ubiquitin remnant with dimethylated Arg" RELATED []
-xref: record_id "1829"
-xref: delta_mono_mass "411.259403"
-xref: delta_avge_mass "411.4991"
-xref: delta_composition "H(33) C(18) N(7) O(4)"
-xref: username_of_poster "bkatja"
-xref: group_of_poster ""
-xref: date_time_posted "2016-07-27 16:20:40"
-xref: date_time_modified "2016-09-23 13:43:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1830
-name: Biotin-tyramide
-def: "Biotin-Phenol." [PMID:29039416, URL:http\://www.iris-biotech.de/ls-3500, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1830]
-xref: record_id "1830"
-xref: delta_mono_mass "361.146012"
-xref: delta_avge_mass "361.4585"
-xref: delta_composition "H(23) C(18) N(3) O(3) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2016-08-04 08:05:43"
-xref: date_time_modified "2023-02-24 12:26:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_2_misc_notes "Only observed on a small fraction of residues (~2%). See doi: 10.1038/nmeth.4465"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "W"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_misc_notes "Only observed on a small fraction of residues (~2%). See doi: 10.1038/nmeth.4465"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1831
-name: Tris
-def: "Tris adduct causes 104 Da addition at asparagine-succinimide intermediate." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1831]
-synonym: "tris adduct at IgG causes 104 Da addition tris adduct at asparagine" RELATED []
-xref: record_id "1831"
-xref: delta_mono_mass "104.071154"
-xref: delta_avge_mass "104.1277"
-xref: delta_composition "H(10) C(4) N O(2)"
-xref: username_of_poster "pradeepnpraveen"
-xref: group_of_poster ""
-xref: date_time_posted "2016-08-04 12:54:25"
-xref: date_time_modified "2024-08-12 09:58:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_misc_notes "NG sequence specifically after deamidation - Deamidated Asparagine with adjacent glycine are prone for this modification."
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1832
-name: IASD
-def: "Iodoacetamide derivative of stilbene (reaction product with thiol)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1832]
-synonym: "4-acetamido-4'-((iodoacetyl)amino)stilbene-2,2'-disulfonic acid" RELATED []
-xref: record_id "1832"
-xref: delta_mono_mass "452.034807"
-xref: delta_avge_mass "452.4582"
-xref: delta_composition "H(16) C(18) N(2) O(8) S(2)"
-xref: username_of_poster "AberdeenProteomics"
-xref: group_of_poster ""
-xref: date_time_posted "2016-08-05 12:04:02"
-xref: date_time_modified "2016-09-23 13:49:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1833
-name: NP40
-def: "NP-40 synthetic polymer terminus." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1833]
-xref: record_id "1833"
-xref: delta_mono_mass "220.182715"
-xref: delta_avge_mass "220.3505"
-xref: delta_composition "H(24) C(15) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2016-08-22 14:48:48"
-xref: date_time_modified "2016-08-22 16:07:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1834
-name: Tween20
-def: "Tween 20 synthetic polymer terminus." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1834]
-xref: record_id "1834"
-xref: delta_mono_mass "165.164326"
-xref: delta_avge_mass "165.2951"
-xref: delta_composition "H(21) C(12)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2016-08-22 14:51:41"
-xref: date_time_modified "2016-08-22 16:07:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1835
-name: Tween80
-def: "Tween 80 synthetic polymer terminus." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1835]
-xref: record_id "1835"
-xref: delta_mono_mass "263.237491"
-xref: delta_avge_mass "263.4381"
-xref: delta_composition "H(31) C(18) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2016-08-22 14:52:52"
-xref: date_time_modified "2016-08-22 16:08:10"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Any C-term"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1836
-name: Triton
-def: "Triton synthetic polymer terminus." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1836]
-xref: record_id "1836"
-xref: delta_mono_mass "188.156501"
-xref: delta_avge_mass "188.3086"
-xref: delta_composition "H(20) C(14)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2016-08-22 14:53:44"
-xref: date_time_modified "2016-08-22 16:07:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Any C-term"
-xref: spec_1_classification "Other"
-xref: spec_1_misc_notes "Triton X-100"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Other"
-xref: spec_2_misc_notes "Triton X-114"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1837
-name: Brij35
-def: "Brij 35 synthetic polymer terminus." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1837]
-xref: record_id "1837"
-xref: delta_mono_mass "168.187801"
-xref: delta_avge_mass "168.319"
-xref: delta_composition "H(24) C(12)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2016-08-22 14:55:48"
-xref: date_time_modified "2016-08-22 16:07:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1838
-name: Brij58
-def: "Brij 58 synthetic polymer terminus." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1838]
-xref: record_id "1838"
-xref: delta_mono_mass "224.250401"
-xref: delta_avge_mass "224.4253"
-xref: delta_composition "H(32) C(16)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2016-08-22 14:56:22"
-xref: date_time_modified "2016-08-22 16:08:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1839
-name: betaFNA
-def: "Beta-Funaltrexamine." [PMID:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3523197/, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1839]
-comment: Covalently bound structure in Manglik et al., Fig. 1b-Fig1c. Chemical formula % Sigma catalog entry.
-xref: record_id "1839"
-xref: delta_mono_mass "454.210387"
-xref: delta_avge_mass "454.5155"
-xref: delta_composition "H(30) C(25) N(2) O(6)"
-xref: username_of_poster "shartson"
-xref: group_of_poster ""
-xref: date_time_posted "2016-08-26 19:59:17"
-xref: date_time_modified "2024-08-12 10:21:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1840
-name: dHex(1)Hex(7)HexNAc(4)
-def: "Fucosylated biantennary + 2 alphaGal." [PMID:http://www.ncbi.nlm.nih.gov/pubmed/23924801, URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=7&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1840]
-xref: record_id "1840"
-xref: delta_mono_mass "2092.745164"
-xref: delta_avge_mass "2093.8955"
-xref: delta_composition "dHex Hex(7) HexNAc(4)"
-xref: username_of_poster "suckau"
-xref: group_of_poster ""
-xref: date_time_posted "2016-09-05 15:52:53"
-xref: date_time_modified "2016-09-09 16:57:21"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_misc_notes "observed in monoclonal antibodies"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1841
-name: Biotin:Thermo-21328
-def: "EZ-Link Sulfo-NHS-SS-Biotin." [URL:https\://tools.thermofisher.com/content/sfs/manuals/MAN0011183_EZ_SulfoNHS_SS_Biotin_UG.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1841]
-synonym: "also Biotin:Thermo-21331" RELATED []
-xref: record_id "1841"
-xref: delta_mono_mass "389.090154"
-xref: delta_avge_mass "389.5564"
-xref: delta_composition "H(23) C(15) N(3) O(3) S(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2016-11-11 10:34:53"
-xref: date_time_modified "2016-11-11 10:36:26"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1843
-name: PhosphoCytidine
-def: "Cytidine monophosphate." [URL:dx.doi.org/10.1038/nchembio0609-378, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1843]
-comment: By analogy with AMP.
-synonym: "CMP" RELATED []
-xref: record_id "1843"
-xref: delta_mono_mass "305.041287"
-xref: delta_avge_mass "305.1812"
-xref: delta_composition "H(12) C(9) N(3) O(7) P"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-02-01 17:36:16"
-xref: date_time_modified "2017-02-02 10:16:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1845
-name: AzidoF
-def: "Azidophenylalanine." [PMID:26597962, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1845]
-xref: record_id "1845"
-xref: delta_mono_mass "41.001397"
-xref: delta_avge_mass "41.0122"
-xref: delta_composition "H(-1) N(3)"
-xref: username_of_poster "astridb"
-xref: group_of_poster ""
-xref: date_time_posted "2017-02-17 09:53:27"
-xref: date_time_modified "2017-03-03 15:46:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1846
-name: Dimethylaminoethyl
-def: "Cys alkylation by dimethylaminoethyl halide." [PMID:20373501, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1846]
-xref: record_id "1846"
-xref: delta_mono_mass "71.073499"
-xref: delta_avge_mass "71.121"
-xref: delta_composition "H(9) C(4) N"
-xref: username_of_poster "Kramerh"
-xref: group_of_poster ""
-xref: date_time_posted "2017-02-17 16:10:59"
-xref: date_time_modified "2017-03-03 15:50:09"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1848
-name: Gluratylation
-def: "Glutarylation." [PMID:24703693, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1848]
-xref: record_id "1848"
-xref: delta_mono_mass "114.031694"
-xref: delta_avge_mass "114.0993"
-xref: delta_composition "H(6) C(5) O(3)"
-xref: username_of_poster "cfeller"
-xref: group_of_poster ""
-xref: date_time_posted "2017-03-30 11:15:26"
-xref: date_time_modified "2017-04-05 12:31:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1849
-name: hydroxyisobutyryl
-def: "2-hydroxyisobutyrylation." [PMID:24681537, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1849]
-synonym: "2-hydroxyisobutanoyl 3-hydroxybutanoyl" RELATED []
-xref: record_id "1849"
-xref: delta_mono_mass "86.036779"
-xref: delta_avge_mass "86.0892"
-xref: delta_composition "H(6) C(4) O(2)"
-xref: username_of_poster "cfeller"
-xref: group_of_poster ""
-xref: date_time_posted "2017-03-30 11:16:14"
-xref: date_time_modified "2021-03-11 11:57:59"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1868
-name: MeMePhosphorothioate
-def: "S-Methyl Methyl phosphorothioate." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1868]
-xref: record_id "1868"
-xref: delta_mono_mass "107.979873"
-xref: delta_avge_mass "108.0993"
-xref: delta_composition "H(5) C(2) O P S"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2017-04-11 18:32:43"
-xref: date_time_modified "2017-06-02 16:01:58"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1870
-name: Cation:Fe[III]
-def: "Replacement of 3 protons by iron." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1870]
-xref: record_id "1870"
-xref: delta_mono_mass "52.911464"
-xref: delta_avge_mass "52.8212"
-xref: delta_composition "H(-3) Fe"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-06-15 12:58:58"
-xref: date_time_modified "2024-08-12 09:58:26"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1871
-name: DTT
-def: "DTT adduct of cysteine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1871]
-xref: record_id "1871"
-xref: delta_mono_mass "151.996571"
-xref: delta_avge_mass "152.2351"
-xref: delta_composition "H(8) C(4) O(2) S(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-06-15 14:09:46"
-xref: date_time_modified "2024-08-12 09:58:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1872
-name: DYn-2
-def: "Sulfenic Acid specific probe." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1872]
-xref: record_id "1872"
-xref: delta_mono_mass "161.09664"
-xref: delta_avge_mass "161.2203"
-xref: delta_composition "H(13) C(11) O"
-xref: username_of_poster "SamanthaLapehn"
-xref: group_of_poster ""
-xref: date_time_posted "2017-07-06 17:23:58"
-xref: date_time_modified "2017-08-05 02:16:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_1_misc_notes "-SOH"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1873
-name: MesitylOxide
-def: "Acetone chemical artifact." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1873]
-xref: record_id "1873"
-xref: delta_mono_mass "98.073165"
-xref: delta_avge_mass "98.143"
-xref: delta_composition "H(10) C(6) O"
-xref: username_of_poster "mlefers"
-xref: group_of_poster ""
-xref: date_time_posted "2017-07-13 19:50:51"
-xref: date_time_modified "2017-08-04 17:22:43"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1875
-name: methylol
-def: "Formaldehyde induced modifications." [PMID:https://www.ncbi.nlm.nih.gov/pubmed/16704222, PMID:https://www.ncbi.nlm.nih.gov/pubmed/14638685, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1875]
-xref: record_id "1875"
-xref: delta_mono_mass "30.010565"
-xref: delta_avge_mass "30.026"
-xref: delta_composition "H(2) C O"
-xref: username_of_poster "robertyen"
-xref: group_of_poster ""
-xref: date_time_posted "2017-07-14 18:43:02"
-xref: date_time_modified "2017-08-04 17:27:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "W"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1877
-name: Xlink:DSS[259]
-def: "Tris-quenched monolink of DSS/BS3 crosslinker." [PMID:8326953, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1877]
-xref: record_id "1877"
-xref: delta_mono_mass "259.141973"
-xref: delta_avge_mass "259.2988"
-xref: delta_composition "H(21) C(12) N O(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-17 14:29:30"
-xref: date_time_modified "2017-08-17 15:09:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1878
-name: Xlink:DSSO[176]
-def: "Water-quenched monolink of DSSO crosslinker." [URL:https\://www.thermofisher.com/order/catalog/product/A33545, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1878]
-xref: record_id "1878"
-xref: delta_mono_mass "176.01433"
-xref: delta_avge_mass "176.1903"
-xref: delta_composition "H(8) C(6) O(4) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-17 16:26:01"
-xref: date_time_modified "2017-08-17 16:26:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1879
-name: Xlink:DSSO[175]
-def: "Ammonia-quenched monolink of DSSO crosslinker." [URL:https\://www.thermofisher.com/order/catalog/product/A33545, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1879]
-xref: record_id "1879"
-xref: delta_mono_mass "175.030314"
-xref: delta_avge_mass "175.2056"
-xref: delta_composition "H(9) C(6) N O(3) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-17 16:27:45"
-xref: date_time_modified "2017-08-17 16:27:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1880
-name: Xlink:DSSO[279]
-def: "Tris-quenched monolink of DSSO crosslinker." [URL:https\://www.thermofisher.com/order/catalog/product/A33545, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1880]
-xref: record_id "1880"
-xref: delta_mono_mass "279.077658"
-xref: delta_avge_mass "279.3101"
-xref: delta_composition "H(17) C(10) N O(6) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-17 16:29:08"
-xref: date_time_modified "2017-08-17 16:29:08"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1881
-name: Xlink:DSSO[54]
-def: "Alkene fragment of DSSO crosslinker." [URL:https\://www.thermofisher.com/order/catalog/product/A33545, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1881]
-xref: record_id "1881"
-xref: delta_mono_mass "54.010565"
-xref: delta_avge_mass "54.0474"
-xref: delta_composition "H(2) C(3) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-17 16:31:03"
-xref: date_time_modified "2017-08-17 16:31:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1882
-name: Xlink:DSSO[86]
-def: "Thiol fragment of DSSO crosslinker." [URL:https\://www.thermofisher.com/order/catalog/product/A33545, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1882]
-xref: record_id "1882"
-xref: delta_mono_mass "85.982635"
-xref: delta_avge_mass "86.1124"
-xref: delta_composition "H(2) C(3) O S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-17 16:32:17"
-xref: date_time_modified "2017-08-17 16:32:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1883
-name: Xlink:DSSO[104]
-def: "Sulfenic acid fragment of DSSO crosslinker." [URL:https\://www.thermofisher.com/order/catalog/product/A33545, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1883]
-xref: record_id "1883"
-xref: delta_mono_mass "103.9932"
-xref: delta_avge_mass "104.1277"
-xref: delta_composition "H(4) C(3) O(2) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-17 16:33:16"
-xref: date_time_modified "2017-08-17 16:33:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1885
-name: Xlink:BuUrBu[111]
-def: "BuUr fragment of BuUrBu crosslinker." [URL:https\://www.thermofisher.com/order/catalog/product/A35459, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1885]
-xref: record_id "1885"
-xref: delta_mono_mass "111.032028"
-xref: delta_avge_mass "111.0987"
-xref: delta_composition "H(5) C(5) N O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-18 09:34:59"
-xref: date_time_modified "2024-08-12 10:24:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "S"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1886
-name: Xlink:BuUrBu[85]
-def: "Bu fragment of BuUrBu crosslinker." [URL:https\://www.thermofisher.com/order/catalog/product/A35459, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1886]
-xref: record_id "1886"
-xref: delta_mono_mass "85.052764"
-xref: delta_avge_mass "85.1045"
-xref: delta_composition "H(7) C(4) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-18 09:36:27"
-xref: date_time_modified "2024-08-12 10:23:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "S"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1887
-name: Xlink:BuUrBu[213]
-def: "Ammonia quenched monolink of BuUrBu crosslinker." [URL:https\://www.thermofisher.com/order/catalog/product/A35459, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1887]
-xref: record_id "1887"
-xref: delta_mono_mass "213.111341"
-xref: delta_avge_mass "213.2337"
-xref: delta_composition "H(15) C(9) N(3) O(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-18 09:38:52"
-xref: date_time_modified "2024-08-12 10:23:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "S"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1888
-name: Xlink:BuUrBu[214]
-def: "Water quenched monolink of BuUrBu crosslinker." [URL:https\://www.thermofisher.com/order/catalog/product/A35459, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1888]
-xref: record_id "1888"
-xref: delta_mono_mass "214.095357"
-xref: delta_avge_mass "214.2185"
-xref: delta_composition "H(14) C(9) N(2) O(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-18 09:43:05"
-xref: date_time_modified "2024-08-12 10:23:14"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "S"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1889
-name: Xlink:BuUrBu[317]
-def: "Tris quenched monolink of BuUrBu crosslinker." [URL:https\://www.thermofisher.com/order/catalog/product/A35459, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1889]
-xref: record_id "1889"
-xref: delta_mono_mass "317.158686"
-xref: delta_avge_mass "317.3382"
-xref: delta_composition "H(23) C(13) N(3) O(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-18 09:44:40"
-xref: date_time_modified "2024-08-12 10:22:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "S"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1896
-name: Xlink:DSSO[158]
-def: "Intact DSSO crosslinker." [URL:https\://www.thermofisher.com/order/catalog/product/A33545, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1896]
-xref: record_id "1896"
-xref: delta_mono_mass "158.003765"
-xref: delta_avge_mass "158.175"
-xref: delta_composition "H(6) C(6) O(3) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-31 14:53:02"
-xref: date_time_modified "2017-08-31 14:53:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1897
-name: Xlink:EGS[226]
-def: "Intact EGS cross-linker." [PMID:36892, URL:https\://tools.thermofisher.com/content/sfs/manuals/MAN0011281_EGS_SulfoEGS_UG.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1897]
-synonym: "Ethylene glycolbis(succinimidylsuccinate)" RELATED []
-xref: record_id "1897"
-xref: delta_mono_mass "226.047738"
-xref: delta_avge_mass "226.1828"
-xref: delta_composition "H(10) C(10) O(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-31 14:54:57"
-xref: date_time_modified "2017-08-31 14:54:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1898
-name: Xlink:DSS[138]
-def: "Intact DSS/BS3 crosslinker." [PMID:8326953, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1898]
-xref: record_id "1898"
-xref: delta_mono_mass "138.06808"
-xref: delta_avge_mass "138.1638"
-xref: delta_composition "H(10) C(8) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-31 14:55:56"
-xref: date_time_modified "2017-08-31 14:55:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1899
-name: Xlink:BuUrBu[196]
-def: "Intact BuUrBu crosslinker." [URL:https\://www.thermofisher.com/order/catalog/product/A35459, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1899]
-xref: record_id "1899"
-xref: delta_mono_mass "196.084792"
-xref: delta_avge_mass "196.2032"
-xref: delta_composition "H(12) C(9) N(2) O(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-31 14:57:02"
-xref: date_time_modified "2024-08-12 10:22:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "S"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1900
-name: Xlink:DTBP[172]
-def: "Intact DTBP crosslinker." [PMID:770170, URL:http\://tools.thermofisher.com/content/sfs/manuals/MAN0011314_ImidoesterCrsLnk_DMA_DMP_DMS_DTBP_UG.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1900]
-comment: Imidoester cross-linker.
-synonym: "dimethyl 3,3'-dithiobispropionimidate" RELATED []
-xref: record_id "1900"
-xref: delta_mono_mass "172.01289"
-xref: delta_avge_mass "172.2711"
-xref: delta_composition "H(8) C(6) N(2) S(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-31 14:59:08"
-xref: date_time_modified "2017-08-31 14:59:08"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1901
-name: Xlink:DST[114]
-def: "Intact DST crosslinker." [PMID:212103, URL:https\://assets.thermofisher.com/TFS-Assets/LSG/manuals/MAN0011282_DST_UG.pdf, PMID:3001048, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1901]
-xref: record_id "1901"
-xref: delta_mono_mass "113.995309"
-xref: delta_avge_mass "114.0563"
-xref: delta_composition "H(2) C(4) O(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-31 15:00:13"
-xref: date_time_modified "2017-08-31 15:00:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1902
-name: Xlink:DTSSP[174]
-def: "Intact DSP/DTSSP crosslinker." [URL:https\://tools.thermofisher.com/content/sfs/manuals/MAN0011280_DTSSP_DSP_UG.pdf, PMID:1262347, PMID:8457554, PMID:322714, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1902]
-synonym: "Also known as DSP" RELATED []
-xref: record_id "1902"
-xref: delta_mono_mass "173.980921"
-xref: delta_avge_mass "174.2406"
-xref: delta_composition "H(6) C(6) O(2) S(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-31 15:01:08"
-xref: date_time_modified "2017-08-31 15:01:08"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1903
-name: Xlink:SMCC[219]
-def: "Intact SMCC cross-link." [URL:https\://assets.thermofisher.com/TFS-Assets/LSG/manuals/MAN0011295_SMCC_SulfoSMCC_UG.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1903]
-xref: record_id "1903"
-xref: delta_mono_mass "219.089543"
-xref: delta_avge_mass "219.2365"
-xref: delta_composition "H(13) C(12) N O(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-31 15:02:14"
-xref: date_time_modified "2017-09-05 15:00:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1905
-name: Xlink:BS2G[96]
-def: "Intact BS2-G crosslinker." [URL:https\://assets.thermofisher.com/TFS-Assets/LSG/manuals/MAN0011542_BS3_d0d4_BS2G_d0d3_UG.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1905]
-xref: record_id "1905"
-xref: delta_mono_mass "96.021129"
-xref: delta_avge_mass "96.0841"
-xref: delta_composition "H(4) C(5) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-09-05 16:22:19"
-xref: date_time_modified "2017-09-05 16:22:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1906
-name: Xlink:BS2G[113]
-def: "Ammonium-quenched monolink of BS2-G crosslinker." [URL:https\://assets.thermofisher.com/TFS-Assets/LSG/manuals/MAN0011542_BS3_d0d4_BS2G_d0d3_UG.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1906]
-xref: record_id "1906"
-xref: delta_mono_mass "113.047679"
-xref: delta_avge_mass "113.1146"
-xref: delta_composition "H(7) C(5) N O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-09-05 16:26:19"
-xref: date_time_modified "2017-09-05 16:26:36"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1907
-name: Xlink:BS2G[114]
-def: "Water-quenched monolink of BS2-G crosslinker." [URL:https\://assets.thermofisher.com/TFS-Assets/LSG/manuals/MAN0011542_BS3_d0d4_BS2G_d0d3_UG.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1907]
-xref: record_id "1907"
-xref: delta_mono_mass "114.031694"
-xref: delta_avge_mass "114.0993"
-xref: delta_composition "H(6) C(5) O(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-09-05 16:27:03"
-xref: date_time_modified "2017-09-05 16:27:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1908
-name: Xlink:BS2G[217]
-def: "Tris-quenched monolink of BS2-G crosslinker." [URL:https\://assets.thermofisher.com/TFS-Assets/LSG/manuals/MAN0011542_BS3_d0d4_BS2G_d0d3_UG.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1908]
-xref: record_id "1908"
-xref: delta_mono_mass "217.095023"
-xref: delta_avge_mass "217.2191"
-xref: delta_composition "H(15) C(9) N O(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-09-05 16:28:28"
-xref: date_time_modified "2017-09-05 16:28:43"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1910
-name: Cation:Al[III]
-def: "Replacement of 3 protons by aluminium." [URL:http\://www.matrixscience.com/blog/trying-to-illuminate-proteomics-dark-matter.html, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1910]
-xref: record_id "1910"
-xref: delta_mono_mass "23.958063"
-xref: delta_avge_mass "23.9577"
-xref: delta_composition "H(-3) Al"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-09-05 17:13:59"
-xref: date_time_modified "2017-09-05 17:13:59"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1911
-name: Xlink:DMP[139]
-def: "Ammonia quenched monolink of DMP crosslinker." [PMID:2144419, PMID:14696200, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1911]
-synonym: "Dimethyl pimelimidate dead-end crosslink" RELATED []
-xref: record_id "1911"
-xref: delta_mono_mass "139.110947"
-xref: delta_avge_mass "139.1982"
-xref: delta_composition "H(13) C(7) N(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-09-06 10:03:30"
-xref: date_time_modified "2017-09-06 10:03:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1912
-name: Xlink:DMP[122]
-def: "Intact DMP crosslinker." [PMID:2144419, PMID:14696200, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1912]
-synonym: "Dimethyl pimelimidate" RELATED []
-xref: record_id "1912"
-xref: delta_mono_mass "122.084398"
-xref: delta_avge_mass "122.1677"
-xref: delta_composition "H(10) C(7) N(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-09-06 10:04:39"
-xref: date_time_modified "2017-09-06 10:04:39"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1913
-name: glyoxalAGE
-def: "Glyoxal-derived AGE." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1913]
-xref: record_id "1913"
-xref: delta_mono_mass "21.98435"
-xref: delta_avge_mass "22.0055"
-xref: delta_composition "H(-2) C(2)"
-xref: username_of_poster "mlefers"
-xref: group_of_poster ""
-xref: date_time_posted "2017-10-05 13:54:48"
-xref: date_time_modified "2017-11-08 17:25:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1914
-name: Met->AspSA
-def: "Methionine oxidation to aspartic semialdehyde." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1914]
-xref: record_id "1914"
-xref: delta_mono_mass "-32.008456"
-xref: delta_avge_mass "-32.1081"
-xref: delta_composition "H(-4) C(-1) O S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-10-06 15:35:18"
-xref: date_time_modified "2017-10-06 15:37:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1915
-name: Decarboxylation
-def: "Decarboxylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1915]
-xref: record_id "1915"
-xref: delta_mono_mass "-30.010565"
-xref: delta_avge_mass "-30.026"
-xref: delta_composition "H(-2) C(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-10-06 15:40:31"
-xref: date_time_modified "2017-10-06 15:40:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "E"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1916
-name: Aspartylurea
-def: "Aspartylurea." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1916]
-xref: record_id "1916"
-xref: delta_mono_mass "-10.031969"
-xref: delta_avge_mass "-10.0412"
-xref: delta_composition "H(-2) C(-1) N(-2) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-10-06 15:43:52"
-xref: date_time_modified "2017-10-06 15:43:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1917
-name: Formylasparagine
-def: "In Bachi as Formylaspargine (typo?)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1917]
-xref: record_id "1917"
-xref: delta_mono_mass "4.97893"
-xref: delta_avge_mass "4.9735"
-xref: delta_composition "H(-1) C(-1) N(-1) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-10-06 16:01:29"
-xref: date_time_modified "2017-11-02 17:23:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1918
-name: Carbonyl
-def: "Aldehyde and ketone modifications." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1918]
-xref: record_id "1918"
-xref: delta_mono_mass "13.979265"
-xref: delta_avge_mass "13.9835"
-xref: delta_composition "H(-2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-10-06 16:09:53"
-xref: date_time_modified "2017-10-06 16:12:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "E"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "I"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "L"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "Q"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "R"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "S"
-xref: spec_7_position "Anywhere"
-xref: spec_7_classification "Chemical derivative"
-xref: spec_8_group "8"
-xref: spec_8_hidden "1"
-xref: spec_8_site "V"
-xref: spec_8_position "Anywhere"
-xref: spec_8_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1920
-name: AFB1_Dialdehyde
-def: "Adduction of aflatoxin B1 Dialdehyde to lysine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1920]
-xref: record_id "1920"
-xref: delta_mono_mass "310.047738"
-xref: delta_avge_mass "310.2577"
-xref: delta_composition "H(10) C(17) O(6)"
-xref: username_of_poster "shenmic"
-xref: group_of_poster ""
-xref: date_time_posted "2017-10-17 14:58:16"
-xref: date_time_modified "2024-08-12 09:57:33"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1922
-name: Pro->HAVA
-def: "Proline oxidation to 5-hydroxy-2-aminovaleric acid." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1922]
-xref: record_id "1922"
-xref: delta_mono_mass "18.010565"
-xref: delta_avge_mass "18.0153"
-xref: delta_composition "H(2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-03 09:13:16"
-xref: date_time_modified "2017-11-03 09:13:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1923
-name: Delta:H(-4)O(2)
-def: "Tryptophan oxidation to beta-unsaturated-2,4-bis-tryptophandione." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1923]
-xref: record_id "1923"
-xref: delta_mono_mass "27.958529"
-xref: delta_avge_mass "27.967"
-xref: delta_composition "H(-4) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-03 09:17:12"
-xref: date_time_modified "2017-11-08 17:00:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1924
-name: Delta:H(-4)O(3)
-def: "Tryptophan oxidation to hydroxy-bis-tryptophandione." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1924]
-xref: record_id "1924"
-xref: delta_mono_mass "43.953444"
-xref: delta_avge_mass "43.9664"
-xref: delta_composition "H(-4) O(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-08 16:11:21"
-xref: date_time_modified "2017-11-08 17:01:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1925
-name: Delta:O(4)
-def: "Tryptophan oxidation to dihydroxy-N-formaylkynurenine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1925]
-xref: record_id "1925"
-xref: delta_mono_mass "63.979659"
-xref: delta_avge_mass "63.9976"
-xref: delta_composition "O(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-08 16:33:11"
-xref: date_time_modified "2017-11-08 17:01:29"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1926
-name: Delta:H(4)C(3)O(2)
-def: "Methylglyoxal-derived carboxyethyllysine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1926]
-xref: record_id "1926"
-xref: delta_mono_mass "72.021129"
-xref: delta_avge_mass "72.0627"
-xref: delta_composition "H(4) C(3) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-08 16:41:02"
-xref: date_time_modified "2021-06-30 11:32:08"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_misc_notes "Note that Table 3 in the reference has the delta as H(3) C(3) O(2) = 71 Da"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1927
-name: Delta:H(4)C(5)O(1)
-def: "Methylglyoxal-derived argpyrimidine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1927]
-xref: record_id "1927"
-xref: delta_mono_mass "80.026215"
-xref: delta_avge_mass "80.0847"
-xref: delta_composition "H(4) C(5) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-08 16:43:41"
-xref: date_time_modified "2018-06-26 10:38:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1928
-name: Delta:H(10)C(8)O(1)
-def: "Crotonaldehyde-derived dimethyl-FDP-lysine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1928]
-xref: record_id "1928"
-xref: delta_mono_mass "122.073165"
-xref: delta_avge_mass "122.1644"
-xref: delta_composition "H(10) C(8) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-08 17:04:01"
-xref: date_time_modified "2017-11-08 17:04:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1929
-name: Delta:H(6)C(7)O(4)
-def: "Methylglyoxal-derived tetrahydropyrimidine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1929]
-xref: record_id "1929"
-xref: delta_mono_mass "154.026609"
-xref: delta_avge_mass "154.1201"
-xref: delta_composition "H(6) C(7) O(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-08 17:12:02"
-xref: date_time_modified "2017-11-08 17:12:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1930
-name: Pent(2)
-def: "Pent(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?pent=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1930]
-xref: record_id "1930"
-xref: delta_mono_mass "264.084518"
-xref: delta_avge_mass "264.2292"
-xref: delta_composition "Pent(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-23 12:05:50"
-xref: date_time_modified "2017-11-23 13:01:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_265_mono_mass "264.084518"
-xref: spec_1_neutral_loss_265_avge_mass "264.2292"
-xref: spec_1_neutral_loss_265_flag "false"
-xref: spec_1_neutral_loss_265_composition "Pent(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_265_mono_mass "264.084518"
-xref: spec_1_neutral_loss_265_avge_mass "264.2292"
-xref: spec_1_neutral_loss_265_flag "false"
-xref: spec_1_neutral_loss_265_composition "Pent(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1931
-name: Pent(1)HexNAc(1)
-def: "Pent HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?pent=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1931]
-xref: record_id "1931"
-xref: delta_mono_mass "335.121631"
-xref: delta_avge_mass "335.3071"
-xref: delta_composition "Pent HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-23 13:00:37"
-xref: date_time_modified "2017-11-23 13:05:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_336_mono_mass "335.121631"
-xref: spec_1_neutral_loss_336_avge_mass "335.3071"
-xref: spec_1_neutral_loss_336_flag "false"
-xref: spec_1_neutral_loss_336_composition "Pent HexNAc"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_336_mono_mass "335.121631"
-xref: spec_1_neutral_loss_336_avge_mass "335.3071"
-xref: spec_1_neutral_loss_336_flag "false"
-xref: spec_1_neutral_loss_336_composition "Pent HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1932
-name: Hex(2)Sulf(1)
-def: "Hex(2) O(3) S." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1932]
-xref: record_id "1932"
-xref: delta_mono_mass "404.062462"
-xref: delta_avge_mass "404.3444"
-xref: delta_composition "O(3) S Hex(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-23 15:39:42"
-xref: date_time_modified "2017-11-23 15:40:36"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_405_mono_mass "404.062462"
-xref: spec_1_neutral_loss_405_avge_mass "404.3444"
-xref: spec_1_neutral_loss_405_flag "false"
-xref: spec_1_neutral_loss_405_composition "O(3) S Hex(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_405_mono_mass "404.062462"
-xref: spec_1_neutral_loss_405_avge_mass "404.3444"
-xref: spec_1_neutral_loss_405_flag "false"
-xref: spec_1_neutral_loss_405_composition "O(3) S Hex(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1933
-name: Hex(1)Pent(2)Me(1)
-def: "Hex:1 Pent:2 Me:1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?methyl=1&pent=2&hex=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1933]
-xref: record_id "1933"
-xref: delta_mono_mass "440.152991"
-xref: delta_avge_mass "440.3964"
-xref: delta_composition "Me Pent(2) Hex"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-23 15:47:22"
-xref: date_time_modified "2017-11-23 15:49:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_441_mono_mass "440.152991"
-xref: spec_1_neutral_loss_441_avge_mass "440.3964"
-xref: spec_1_neutral_loss_441_flag "false"
-xref: spec_1_neutral_loss_441_composition "Me Pent(2) Hex"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_441_mono_mass "440.152991"
-xref: spec_1_neutral_loss_441_avge_mass "440.3964"
-xref: spec_1_neutral_loss_441_flag "false"
-xref: spec_1_neutral_loss_441_composition "Me Pent(2) Hex"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1934
-name: HexNAc(2)Sulf(1)
-def: "HexNAc(2) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1934]
-xref: record_id "1934"
-xref: delta_mono_mass "486.11556"
-xref: delta_avge_mass "486.4482"
-xref: delta_composition "O(3) S HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-23 16:35:09"
-xref: date_time_modified "2017-11-23 16:35:09"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_487_mono_mass "486.11556"
-xref: spec_1_neutral_loss_487_avge_mass "486.4482"
-xref: spec_1_neutral_loss_487_flag "false"
-xref: spec_1_neutral_loss_487_composition "O(3) S HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_487_mono_mass "486.11556"
-xref: spec_1_neutral_loss_487_avge_mass "486.4482"
-xref: spec_1_neutral_loss_487_flag "false"
-xref: spec_1_neutral_loss_487_composition "O(3) S HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1935
-name: Hex(1)Pent(3)Me(1)
-def: "Hex Pent(3) Me." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?methyl=1&pent=3&hex=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1935]
-xref: record_id "1935"
-xref: delta_mono_mass "572.19525"
-xref: delta_avge_mass "572.511"
-xref: delta_composition "Me Pent(3) Hex"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-23 16:40:05"
-xref: date_time_modified "2017-11-23 16:40:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_573_mono_mass "572.19525"
-xref: spec_1_neutral_loss_573_avge_mass "572.511"
-xref: spec_1_neutral_loss_573_flag "false"
-xref: spec_1_neutral_loss_573_composition "Me Pent(3) Hex"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_573_mono_mass "572.19525"
-xref: spec_1_neutral_loss_573_avge_mass "572.511"
-xref: spec_1_neutral_loss_573_flag "false"
-xref: spec_1_neutral_loss_573_composition "Me Pent(3) Hex"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1936
-name: Hex(2)Pent(2)
-def: "Hex(2) Pent(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?pent=2&hex=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1936]
-xref: record_id "1936"
-xref: delta_mono_mass "588.190165"
-xref: delta_avge_mass "588.5104"
-xref: delta_composition "Pent(2) Hex(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-23 17:22:55"
-xref: date_time_modified "2017-11-23 17:22:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_589_mono_mass "588.190165"
-xref: spec_1_neutral_loss_589_avge_mass "588.5104"
-xref: spec_1_neutral_loss_589_flag "false"
-xref: spec_1_neutral_loss_589_composition "Pent(2) Hex(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_589_mono_mass "588.190165"
-xref: spec_1_neutral_loss_589_avge_mass "588.5104"
-xref: spec_1_neutral_loss_589_flag "false"
-xref: spec_1_neutral_loss_589_composition "Pent(2) Hex(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1937
-name: Hex(2)Pent(2)Me(1)
-def: "Hex(2) Pent(2) Me." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?methyl=1&pent=2&hex=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1937]
-xref: record_id "1937"
-xref: delta_mono_mass "602.205815"
-xref: delta_avge_mass "602.537"
-xref: delta_composition "Me Pent(2) Hex(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-23 17:24:00"
-xref: date_time_modified "2017-11-23 17:24:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_603_mono_mass "602.205815"
-xref: spec_1_neutral_loss_603_avge_mass "602.537"
-xref: spec_1_neutral_loss_603_flag "false"
-xref: spec_1_neutral_loss_603_composition "Me Pent(2) Hex(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_603_mono_mass "602.205815"
-xref: spec_1_neutral_loss_603_avge_mass "602.537"
-xref: spec_1_neutral_loss_603_flag "false"
-xref: spec_1_neutral_loss_603_composition "Me Pent(2) Hex(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1938
-name: Hex(4)HexA(1)
-def: "Hex(4) HexA." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexa=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1938]
-xref: record_id "1938"
-xref: delta_mono_mass "824.243382"
-xref: delta_avge_mass "824.6865"
-xref: delta_composition "Hex(4) HexA"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-23 17:49:25"
-xref: date_time_modified "2017-11-23 17:49:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_825_mono_mass "824.243382"
-xref: spec_1_neutral_loss_825_avge_mass "824.6865"
-xref: spec_1_neutral_loss_825_flag "false"
-xref: spec_1_neutral_loss_825_composition "Hex(4) HexA"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_825_mono_mass "824.243382"
-xref: spec_1_neutral_loss_825_avge_mass "824.6865"
-xref: spec_1_neutral_loss_825_flag "false"
-xref: spec_1_neutral_loss_825_composition "Hex(4) HexA"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1939
-name: Hex(2)HexNAc(1)Pent(1)HexA(1)
-def: "Hex(2) HexNAc Pent HexA." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?pent=1&hex=2&hexa=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1939]
-xref: record_id "1939"
-xref: delta_mono_mass "835.259366"
-xref: delta_avge_mass "835.7125"
-xref: delta_composition "Pent Hex(2) HexA HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-23 17:51:41"
-xref: date_time_modified "2017-11-23 17:51:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_836_mono_mass "835.259366"
-xref: spec_1_neutral_loss_836_avge_mass "835.7125"
-xref: spec_1_neutral_loss_836_flag "false"
-xref: spec_1_neutral_loss_836_composition "Pent Hex(2) HexA HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_836_mono_mass "835.259366"
-xref: spec_1_neutral_loss_836_avge_mass "835.7125"
-xref: spec_1_neutral_loss_836_flag "false"
-xref: spec_1_neutral_loss_836_composition "Pent Hex(2) HexA HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1940
-name: Hex(3)HexNAc(1)HexA(1)
-def: "Hex(3) HexNAc HexA." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexa=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1940]
-xref: record_id "1940"
-xref: delta_mono_mass "865.269931"
-xref: delta_avge_mass "865.7384"
-xref: delta_composition "Hex(3) HexA HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 10:41:50"
-xref: date_time_modified "2017-11-24 10:41:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_866_mono_mass "865.269931"
-xref: spec_1_neutral_loss_866_avge_mass "865.7384"
-xref: spec_1_neutral_loss_866_flag "false"
-xref: spec_1_neutral_loss_866_composition "Hex(3) HexA HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_866_mono_mass "865.269931"
-xref: spec_1_neutral_loss_866_avge_mass "865.7384"
-xref: spec_1_neutral_loss_866_flag "false"
-xref: spec_1_neutral_loss_866_composition "Hex(3) HexA HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1941
-name: Hex(1)HexNAc(2)dHex(2)Sulf(1)
-def: "Hex HexNAc(2) dHex(2) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=2&hex=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1941]
-xref: record_id "1941"
-xref: delta_mono_mass "940.284201"
-xref: delta_avge_mass "940.8712"
-xref: delta_composition "O(3) S dHex(2) Hex HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 10:45:35"
-xref: date_time_modified "2017-11-24 10:45:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_941_mono_mass "940.284201"
-xref: spec_1_neutral_loss_941_avge_mass "940.8712"
-xref: spec_1_neutral_loss_941_flag "false"
-xref: spec_1_neutral_loss_941_composition "O(3) S dHex(2) Hex HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_941_mono_mass "940.284201"
-xref: spec_1_neutral_loss_941_avge_mass "940.8712"
-xref: spec_1_neutral_loss_941_flag "false"
-xref: spec_1_neutral_loss_941_composition "O(3) S dHex(2) Hex HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1942
-name: HexA(2)HexNAc(3)
-def: "HexA(2) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hexa=2&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1942]
-xref: record_id "1942"
-xref: delta_mono_mass "961.302294"
-xref: delta_avge_mass "961.8258"
-xref: delta_composition "HexA(2) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 10:48:18"
-xref: date_time_modified "2017-11-24 10:48:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_962_mono_mass "961.302294"
-xref: spec_1_neutral_loss_962_avge_mass "961.8258"
-xref: spec_1_neutral_loss_962_flag "false"
-xref: spec_1_neutral_loss_962_composition "HexA(2) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_962_mono_mass "961.302294"
-xref: spec_1_neutral_loss_962_avge_mass "961.8258"
-xref: spec_1_neutral_loss_962_flag "false"
-xref: spec_1_neutral_loss_962_composition "HexA(2) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1943
-name: dHex(1)Hex(4)HexA(1)
-def: "DHex Hex(4) HexA." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=4&hexa=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1943]
-xref: record_id "1943"
-xref: delta_mono_mass "970.301291"
-xref: delta_avge_mass "970.8277"
-xref: delta_composition "dHex Hex(4) HexA"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 10:51:51"
-xref: date_time_modified "2017-11-24 10:52:38"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_971_mono_mass "970.301291"
-xref: spec_1_neutral_loss_971_avge_mass "970.8277"
-xref: spec_1_neutral_loss_971_flag "false"
-xref: spec_1_neutral_loss_971_composition "dHex Hex(4) HexA"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_971_mono_mass "970.301291"
-xref: spec_1_neutral_loss_971_avge_mass "970.8277"
-xref: spec_1_neutral_loss_971_flag "false"
-xref: spec_1_neutral_loss_971_composition "dHex Hex(4) HexA"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1944
-name: Hex(5)HexA(1)
-def: "Hex(5) HexA." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=5&hexa=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1944]
-xref: record_id "1944"
-xref: delta_mono_mass "986.296206"
-xref: delta_avge_mass "986.8271"
-xref: delta_composition "Hex(5) HexA"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 10:54:21"
-xref: date_time_modified "2017-11-24 10:54:21"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_987_mono_mass "986.296206"
-xref: spec_1_neutral_loss_987_avge_mass "986.8271"
-xref: spec_1_neutral_loss_987_flag "false"
-xref: spec_1_neutral_loss_987_composition "Hex(5) HexA"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_987_mono_mass "986.296206"
-xref: spec_1_neutral_loss_987_avge_mass "986.8271"
-xref: spec_1_neutral_loss_987_flag "false"
-xref: spec_1_neutral_loss_987_composition "Hex(5) HexA"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1945
-name: Hex(4)HexA(1)HexNAc(1)
-def: "Hex(4) HexA HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexa=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1945]
-xref: record_id "1945"
-xref: delta_mono_mass "1027.322755"
-xref: delta_avge_mass "1027.879"
-xref: delta_composition "Hex(4) HexA HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 11:02:26"
-xref: date_time_modified "2017-11-24 11:03:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1028_mono_mass "1027.322755"
-xref: spec_1_neutral_loss_1028_avge_mass "1027.879"
-xref: spec_1_neutral_loss_1028_flag "false"
-xref: spec_1_neutral_loss_1028_composition "Hex(4) HexA HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1028_mono_mass "1027.322755"
-xref: spec_1_neutral_loss_1028_avge_mass "1027.879"
-xref: spec_1_neutral_loss_1028_flag "false"
-xref: spec_1_neutral_loss_1028_composition "Hex(4) HexA HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1946
-name: dHex(3)Hex(3)HexNAc(1)
-def: "DHex(3) Hex(3) HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=3&hex=3&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1946]
-xref: record_id "1946"
-xref: delta_mono_mass "1127.41157"
-xref: delta_avge_mass "1128.0379"
-xref: delta_composition "dHex(3) Hex(3) HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 11:05:19"
-xref: date_time_modified "2017-11-24 11:05:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1128_mono_mass "1127.41157"
-xref: spec_1_neutral_loss_1128_avge_mass "1128.0379"
-xref: spec_1_neutral_loss_1128_flag "false"
-xref: spec_1_neutral_loss_1128_composition "dHex(3) Hex(3) HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1128_mono_mass "1127.41157"
-xref: spec_1_neutral_loss_1128_avge_mass "1128.0379"
-xref: spec_1_neutral_loss_1128_flag "false"
-xref: spec_1_neutral_loss_1128_composition "dHex(3) Hex(3) HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1947
-name: Hex(6)HexNAc(1)
-def: "Hex(6) HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=6&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1947]
-xref: record_id "1947"
-xref: delta_mono_mass "1175.396314"
-xref: delta_avge_mass "1176.0361"
-xref: delta_composition "Hex(6) HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 11:50:56"
-xref: date_time_modified "2018-03-28 14:15:08"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1176_mono_mass "1175.396314"
-xref: spec_1_neutral_loss_1176_avge_mass "1176.0361"
-xref: spec_1_neutral_loss_1176_flag "false"
-xref: spec_1_neutral_loss_1176_composition "Hex(6) HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1948
-name: Hex(1)HexNAc(4)dHex(1)Sulf(1)
-def: "Sulf dHex Hex HexNAc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=1&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1948]
-xref: record_id "1948"
-xref: delta_mono_mass "1200.385037"
-xref: delta_avge_mass "1201.1151"
-xref: delta_composition "Sulf dHex Hex HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 11:56:31"
-xref: date_time_modified "2017-11-24 11:57:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1201_mono_mass "1200.385037"
-xref: spec_1_neutral_loss_1201_avge_mass "1201.1151"
-xref: spec_1_neutral_loss_1201_flag "false"
-xref: spec_1_neutral_loss_1201_composition "Sulf dHex Hex HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1201_mono_mass "1200.385037"
-xref: spec_1_neutral_loss_1201_avge_mass "1201.1151"
-xref: spec_1_neutral_loss_1201_flag "false"
-xref: spec_1_neutral_loss_1201_composition "Sulf dHex Hex HexNAc(4)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1949
-name: dHex(1)Hex(2)HexNAc(1)NeuAc(2)
-def: "DHex Hex(2) HexNAc NeuAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=2&hexnac=1&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1949]
-xref: record_id "1949"
-xref: delta_mono_mass "1255.433762"
-xref: delta_avge_mass "1256.1241"
-xref: delta_composition "dHex Hex(2) HexNAc NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 11:58:40"
-xref: date_time_modified "2017-11-24 13:36:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1256_mono_mass "1255.433762"
-xref: spec_1_neutral_loss_1256_avge_mass "1256.1241"
-xref: spec_1_neutral_loss_1256_flag "false"
-xref: spec_1_neutral_loss_1256_composition "dHex Hex(2) HexNAc NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1256_mono_mass "1255.433762"
-xref: spec_1_neutral_loss_1256_avge_mass "1256.1241"
-xref: spec_1_neutral_loss_1256_flag "false"
-xref: spec_1_neutral_loss_1256_composition "dHex Hex(2) HexNAc NeuAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1950
-name: dHex(3)Hex(3)HexNAc(2)
-def: "DHex(3) Hex(3) HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=3&hex=3&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1950]
-xref: record_id "1950"
-xref: delta_mono_mass "1330.490942"
-xref: delta_avge_mass "1331.2304"
-xref: delta_composition "dHex(3) Hex(3) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 12:05:34"
-xref: date_time_modified "2017-11-24 12:06:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1331_mono_mass "1330.490942"
-xref: spec_1_neutral_loss_1331_avge_mass "1331.2304"
-xref: spec_1_neutral_loss_1331_flag "false"
-xref: spec_1_neutral_loss_1331_composition "dHex(3) Hex(3) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1331_mono_mass "1330.490942"
-xref: spec_1_neutral_loss_1331_avge_mass "1331.2304"
-xref: spec_1_neutral_loss_1331_flag "false"
-xref: spec_1_neutral_loss_1331_composition "dHex(3) Hex(3) HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1951
-name: dHex(2)Hex(1)HexNAc(4)Sulf(1)
-def: "DHex(2) Hex HexNAc(4) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=2&hex=1&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1951]
-xref: record_id "1951"
-xref: delta_mono_mass "1346.442946"
-xref: delta_avge_mass "1347.2563"
-xref: delta_composition "Sulf dHex(2) Hex HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 12:07:49"
-xref: date_time_modified "2017-11-24 12:08:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1347_mono_mass "1346.442946"
-xref: spec_1_neutral_loss_1347_avge_mass "1347.2563"
-xref: spec_1_neutral_loss_1347_flag "false"
-xref: spec_1_neutral_loss_1347_composition "Sulf dHex(2) Hex HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1347_mono_mass "1346.442946"
-xref: spec_1_neutral_loss_1347_avge_mass "1347.2563"
-xref: spec_1_neutral_loss_1347_flag "false"
-xref: spec_1_neutral_loss_1347_composition "Sulf dHex(2) Hex HexNAc(4)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1952
-name: dHex(1)Hex(2)HexNAc(4)Sulf(2)
-def: "DHex Hex(2) HexNAc(4) Sulf(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=2&dhex=1&hex=2&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1952]
-xref: record_id "1952"
-xref: delta_mono_mass "1442.394675"
-xref: delta_avge_mass "1443.3189"
-xref: delta_composition "Sulf(2) dHex Hex(2) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 12:56:06"
-xref: date_time_modified "2017-11-24 12:57:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1443_mono_mass "1442.394675"
-xref: spec_1_neutral_loss_1443_avge_mass "1443.3189"
-xref: spec_1_neutral_loss_1443_flag "false"
-xref: spec_1_neutral_loss_1443_composition "Sulf(2) dHex Hex(2) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1443_mono_mass "1442.394675"
-xref: spec_1_neutral_loss_1443_avge_mass "1443.3189"
-xref: spec_1_neutral_loss_1443_flag "false"
-xref: spec_1_neutral_loss_1443_composition "Sulf(2) dHex Hex(2) HexNAc(4)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1953
-name: Hex(9)
-def: "Hex(9)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=9&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1953]
-xref: record_id "1953"
-xref: delta_mono_mass "1458.475412"
-xref: delta_avge_mass "1459.2654"
-xref: delta_composition "Hex(9)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 12:58:01"
-xref: date_time_modified "2017-11-24 12:58:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1459_mono_mass "1458.475412"
-xref: spec_1_neutral_loss_1459_avge_mass "1459.2654"
-xref: spec_1_neutral_loss_1459_flag "false"
-xref: spec_1_neutral_loss_1459_composition "Hex(9)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1954
-name: dHex(2)Hex(3)HexNAc(3)Sulf(1)
-def: "Sulf dHex(2) Hex(3) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=2&hex=3&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1954]
-xref: record_id "1954"
-xref: delta_mono_mass "1467.469221"
-xref: delta_avge_mass "1468.345"
-xref: delta_composition "Sulf dHex(2) Hex(3) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 12:59:19"
-xref: date_time_modified "2017-11-24 13:00:08"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1468_mono_mass "1467.469221"
-xref: spec_1_neutral_loss_1468_avge_mass "1468.345"
-xref: spec_1_neutral_loss_1468_flag "false"
-xref: spec_1_neutral_loss_1468_composition "Sulf dHex(2) Hex(3) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1468_mono_mass "1467.469221"
-xref: spec_1_neutral_loss_1468_avge_mass "1468.345"
-xref: spec_1_neutral_loss_1468_flag "false"
-xref: spec_1_neutral_loss_1468_composition "Sulf dHex(2) Hex(3) HexNAc(3)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1955
-name: dHex(2)Hex(5)HexNAc(2)Me(1)
-def: "Me dHex(2) Hex(5) HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?methyl=1&dhex=2&hex=5&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1955]
-xref: record_id "1955"
-xref: delta_mono_mass "1522.554331"
-xref: delta_avge_mass "1523.397"
-xref: delta_composition "Me dHex(2) Hex(5) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 13:02:33"
-xref: date_time_modified "2017-11-24 13:03:20"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1523_mono_mass "1522.554331"
-xref: spec_1_neutral_loss_1523_avge_mass "1523.397"
-xref: spec_1_neutral_loss_1523_flag "false"
-xref: spec_1_neutral_loss_1523_composition "Me dHex(2) Hex(5) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1523_mono_mass "1522.554331"
-xref: spec_1_neutral_loss_1523_avge_mass "1523.397"
-xref: spec_1_neutral_loss_1523_flag "false"
-xref: spec_1_neutral_loss_1523_composition "Me dHex(2) Hex(5) HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1956
-name: dHex(2)Hex(2)HexNAc(4)Sulf(2)
-def: "Sulf(2) dHex(2) Hex(2) HexNAc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=2&dhex=2&hex=2&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1956]
-xref: record_id "1956"
-xref: delta_mono_mass "1588.452584"
-xref: delta_avge_mass "1589.4601"
-xref: delta_composition "Sulf(2) dHex(2) Hex(2) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 13:04:31"
-xref: date_time_modified "2017-11-24 13:05:20"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1589_mono_mass "1588.452584"
-xref: spec_1_neutral_loss_1589_avge_mass "1589.4601"
-xref: spec_1_neutral_loss_1589_flag "false"
-xref: spec_1_neutral_loss_1589_composition "Sulf(2) dHex(2) Hex(2) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1589_mono_mass "1588.452584"
-xref: spec_1_neutral_loss_1589_avge_mass "1589.4601"
-xref: spec_1_neutral_loss_1589_flag "false"
-xref: spec_1_neutral_loss_1589_composition "Sulf(2) dHex(2) Hex(2) HexNAc(4)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1957
-name: Hex(9)HexNAc(1)
-def: "Hex(9) HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=9&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1957]
-xref: record_id "1957"
-xref: delta_mono_mass "1661.554784"
-xref: delta_avge_mass "1662.4579"
-xref: delta_composition "Hex(9) HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 13:09:44"
-xref: date_time_modified "2017-11-24 13:09:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1662_mono_mass "1661.554784"
-xref: spec_1_neutral_loss_1662_avge_mass "1662.4579"
-xref: spec_1_neutral_loss_1662_flag "false"
-xref: spec_1_neutral_loss_1662_composition "Hex(9) HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1958
-name: dHex(3)Hex(2)HexNAc(4)Sulf(2)
-def: "DHex(3) Hex(2) HexNAc(4) Sulf(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=2&dhex=3&hex=2&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1958]
-xref: record_id "1958"
-xref: delta_mono_mass "1734.510493"
-xref: delta_avge_mass "1735.6013"
-xref: delta_composition "Sulf(2) dHex(3) Hex(2) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 13:31:20"
-xref: date_time_modified "2017-11-24 13:31:20"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1735_mono_mass "1734.510493"
-xref: spec_1_neutral_loss_1735_avge_mass "1735.6013"
-xref: spec_1_neutral_loss_1735_flag "false"
-xref: spec_1_neutral_loss_1735_composition "Sulf(2) dHex(3) Hex(2) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1735_mono_mass "1734.510493"
-xref: spec_1_neutral_loss_1735_avge_mass "1735.6013"
-xref: spec_1_neutral_loss_1735_flag "false"
-xref: spec_1_neutral_loss_1735_composition "Sulf(2) dHex(3) Hex(2) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1959
-name: Hex(4)HexNAc(4)NeuGc(1)
-def: "Hex(4) HexNAc(4) NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexnac=4&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1959]
-xref: record_id "1959"
-xref: delta_mono_mass "1767.619116"
-xref: delta_avge_mass "1768.5865"
-xref: delta_composition "Hex(4) HexNAc(4) NeuGc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 13:33:34"
-xref: date_time_modified "2017-11-24 13:33:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1768_mono_mass "1767.619116"
-xref: spec_1_neutral_loss_1768_avge_mass "1768.5865"
-xref: spec_1_neutral_loss_1768_flag "false"
-xref: spec_1_neutral_loss_1768_composition "Hex(4) HexNAc(4) NeuGc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_1768_mono_mass "1767.619116"
-xref: spec_2_neutral_loss_1768_avge_mass "1768.5865"
-xref: spec_2_neutral_loss_1768_flag "false"
-xref: spec_2_neutral_loss_1768_composition "Hex(4) HexNAc(4) NeuGc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_1768_mono_mass "1767.619116"
-xref: spec_2_neutral_loss_1768_avge_mass "1768.5865"
-xref: spec_2_neutral_loss_1768_flag "false"
-xref: spec_2_neutral_loss_1768_composition "Hex(4) HexNAc(4) NeuGc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1960
-name: dHex(4)Hex(3)HexNAc(2)NeuAc(1)
-def: "DHex(4) Hex(3) HexNAc(2) NeuAc(1)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=4&hex=3&hexnac=2&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1960]
-xref: record_id "1960"
-xref: delta_mono_mass "1767.644268"
-xref: delta_avge_mass "1768.6262"
-xref: delta_composition "dHex(4) Hex(3) HexNAc(2) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 13:39:20"
-xref: date_time_modified "2017-11-24 13:40:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1768_mono_mass "1767.644268"
-xref: spec_1_neutral_loss_1768_avge_mass "1768.6262"
-xref: spec_1_neutral_loss_1768_flag "false"
-xref: spec_1_neutral_loss_1768_composition "dHex(4) Hex(3) HexNAc(2) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1768_mono_mass "1767.644268"
-xref: spec_1_neutral_loss_1768_avge_mass "1768.6262"
-xref: spec_1_neutral_loss_1768_flag "false"
-xref: spec_1_neutral_loss_1768_composition "dHex(4) Hex(3) HexNAc(2) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1961
-name: Hex(3)HexNAc(5)NeuAc(1)
-def: "Hex(3) HexNAc(5) NeuAc(1)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=5&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1961]
-xref: record_id "1961"
-xref: delta_mono_mass "1792.65075"
-xref: delta_avge_mass "1793.639"
-xref: delta_composition "Hex(3) HexNAc(5) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 13:41:14"
-xref: date_time_modified "2017-11-24 13:41:43"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1793_mono_mass "1792.65075"
-xref: spec_1_neutral_loss_1793_avge_mass "1793.639"
-xref: spec_1_neutral_loss_1793_flag "false"
-xref: spec_1_neutral_loss_1793_composition "Hex(3) HexNAc(5) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1962
-name: Hex(10)HexNAc(1)
-def: "Hex(10) HexNAc(1)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=10&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1962]
-xref: record_id "1962"
-xref: delta_mono_mass "1823.607608"
-xref: delta_avge_mass "1824.5985"
-xref: delta_composition "Hex(10) HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 13:46:44"
-xref: date_time_modified "2017-11-24 13:46:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1824_mono_mass "1823.607608"
-xref: spec_1_neutral_loss_1824_avge_mass "1824.5985"
-xref: spec_1_neutral_loss_1824_flag "false"
-xref: spec_1_neutral_loss_1824_composition "Hex(10) HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1963
-name: dHex(1)Hex(8)HexNAc(2)
-def: "DHex Hex(8) HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=8&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1963]
-xref: record_id "1963"
-xref: delta_mono_mass "1848.639242"
-xref: delta_avge_mass "1849.651"
-xref: delta_composition "dHex Hex(8) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 13:48:48"
-xref: date_time_modified "2017-11-24 13:48:48"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1849_mono_mass "1848.639242"
-xref: spec_1_neutral_loss_1849_avge_mass "1849.651"
-xref: spec_1_neutral_loss_1849_flag "false"
-xref: spec_1_neutral_loss_1849_composition "dHex Hex(8) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1964
-name: Hex(3)HexNAc(4)NeuAc(2)
-def: "Hex(3) HexNAc(4) NeuAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=4&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1964]
-xref: record_id "1964"
-xref: delta_mono_mass "1880.666794"
-xref: delta_avge_mass "1881.701"
-xref: delta_composition "Hex(3) HexNAc(4) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 13:50:19"
-xref: date_time_modified "2017-11-24 13:50:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1881_mono_mass "1880.666794"
-xref: spec_1_neutral_loss_1881_avge_mass "1881.701"
-xref: spec_1_neutral_loss_1881_flag "false"
-xref: spec_1_neutral_loss_1881_composition "Hex(3) HexNAc(4) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1965
-name: dHex(2)Hex(3)HexNAc(4)NeuAc(1)
-def: "DHex(2) Hex(3) HexNAc(4) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=3&hexnac=4&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1965]
-xref: record_id "1965"
-xref: delta_mono_mass "1881.687195"
-xref: delta_avge_mass "1882.7289"
-xref: delta_composition "dHex(2) Hex(3) HexNAc(4) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 13:55:45"
-xref: date_time_modified "2017-11-24 13:56:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1882_mono_mass "1881.687195"
-xref: spec_1_neutral_loss_1882_avge_mass "1882.7289"
-xref: spec_1_neutral_loss_1882_flag "false"
-xref: spec_1_neutral_loss_1882_composition "dHex(2) Hex(3) HexNAc(4) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1966
-name: dHex(2)Hex(2)HexNAc(6)Sulf(1)
-def: "DHex(2) Hex(2) HexNAc(6) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=2&hex=2&hexnac=6&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1966]
-xref: record_id "1966"
-xref: delta_mono_mass "1914.654515"
-xref: delta_avge_mass "1915.7819"
-xref: delta_composition "Sulf dHex(2) Hex(2) HexNAc(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 14:01:17"
-xref: date_time_modified "2017-11-24 14:01:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1915_mono_mass "1914.654515"
-xref: spec_1_neutral_loss_1915_avge_mass "1915.7819"
-xref: spec_1_neutral_loss_1915_flag "false"
-xref: spec_1_neutral_loss_1915_composition "Sulf dHex(2) Hex(2) HexNAc(6)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1915_mono_mass "1914.654515"
-xref: spec_1_neutral_loss_1915_avge_mass "1915.7819"
-xref: spec_1_neutral_loss_1915_flag "false"
-xref: spec_1_neutral_loss_1915_composition "Sulf dHex(2) Hex(2) HexNAc(6)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1967
-name: Hex(5)HexNAc(4)NeuAc(1)Ac(1)
-def: "Hex(5) HexNAc(4) NeuAc Ac." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?acetyl=1&hex=5&hexnac=4&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1967]
-xref: record_id "1967"
-xref: delta_mono_mass "1955.687589"
-xref: delta_avge_mass "1956.7643"
-xref: delta_composition "Ac Hex(5) HexNAc(4) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 14:03:24"
-xref: date_time_modified "2017-11-24 14:04:26"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1956_mono_mass "1955.687589"
-xref: spec_1_neutral_loss_1956_avge_mass "1956.7643"
-xref: spec_1_neutral_loss_1956_flag "false"
-xref: spec_1_neutral_loss_1956_composition "Ac Hex(5) HexNAc(4) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1968
-name: Hex(3)HexNAc(3)NeuAc(3)
-def: "Hex(3) HexNAc(3) NeuAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=3&neuac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1968]
-xref: record_id "1968"
-xref: delta_mono_mass "1968.682838"
-xref: delta_avge_mass "1969.7631"
-xref: delta_composition "Hex(3) HexNAc(3) NeuAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 14:05:50"
-xref: date_time_modified "2017-11-24 14:05:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1969_mono_mass "1968.682838"
-xref: spec_1_neutral_loss_1969_avge_mass "1969.7631"
-xref: spec_1_neutral_loss_1969_flag "false"
-xref: spec_1_neutral_loss_1969_composition "Hex(3) HexNAc(3) NeuAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1969_mono_mass "1968.682838"
-xref: spec_1_neutral_loss_1969_avge_mass "1969.7631"
-xref: spec_1_neutral_loss_1969_flag "false"
-xref: spec_1_neutral_loss_1969_composition "Hex(3) HexNAc(3) NeuAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1969
-name: Hex(5)HexNAc(4)NeuAc(1)Ac(2)
-def: "Hex(5) HexNAc(4) NeuAc Ac(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?acetyl=2&hex=5&hexnac=4&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1969]
-xref: record_id "1969"
-xref: delta_mono_mass "1997.698154"
-xref: delta_avge_mass "1998.801"
-xref: delta_composition "Ac(2) Hex(5) HexNAc(4) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 14:06:47"
-xref: date_time_modified "2017-11-24 14:06:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1998_mono_mass "1997.698154"
-xref: spec_1_neutral_loss_1998_avge_mass "1998.801"
-xref: spec_1_neutral_loss_1998_flag "false"
-xref: spec_1_neutral_loss_1998_composition "Ac(2) Hex(5) HexNAc(4) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1970
-name: Unknown:162
-def: "Unidentified modification of 162.1258 found in open search." [URL:http\://www.matrixscience.com/blog/trying-to-illuminate-proteomics-dark-matter.html, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1970]
-synonym: "The elemental composition should be assumed incorrect Although it happens to be that of Diethylene glycol butyl ether, a common solvent." RELATED []
-xref: record_id "1970"
-xref: delta_mono_mass "162.125595"
-xref: delta_avge_mass "162.2267"
-xref: delta_composition "H(18) C(8) O(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-12-07 09:51:01"
-xref: date_time_modified "2018-10-17 14:27:53"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1971
-name: Unknown:177
-def: "Unidentified modification of 176.7462 found in open search." [URL:http\://www.matrixscience.com/blog/trying-to-illuminate-proteomics-dark-matter.html, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1971]
-synonym: "The elemental composition should be assumed incorrect" RELATED []
-xref: record_id "1971"
-xref: delta_mono_mass "176.744957"
-xref: delta_avge_mass "176.4788"
-xref: delta_composition "H(-7) O Fe(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-12-07 09:53:27"
-xref: date_time_modified "2017-12-07 09:53:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1972
-name: Unknown:210
-def: "Unidentified modification of 210.1616 found in open search." [URL:http\://www.matrixscience.com/blog/trying-to-illuminate-proteomics-dark-matter.html, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1972]
-synonym: "The elemental composition should be assumed incorrect" RELATED []
-xref: record_id "1972"
-xref: delta_mono_mass "210.16198"
-xref: delta_avge_mass "210.3126"
-xref: delta_composition "H(22) C(13) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-12-07 09:55:06"
-xref: date_time_modified "2017-12-07 09:55:06"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1973
-name: Unknown:216
-def: "Unidentified modification of 216.1002 found in open search." [URL:http\://www.matrixscience.com/blog/trying-to-illuminate-proteomics-dark-matter.html, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1973]
-synonym: "The elemental composition should be assumed incorrect" RELATED []
-xref: record_id "1973"
-xref: delta_mono_mass "216.099774"
-xref: delta_avge_mass "216.231"
-xref: delta_composition "H(16) C(10) O(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-12-07 09:59:22"
-xref: date_time_modified "2017-12-07 09:59:22"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1974
-name: Unknown:234
-def: "Unidentified modification of 234.0742 found in open search." [URL:http\://www.matrixscience.com/blog/trying-to-illuminate-proteomics-dark-matter.html, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1974]
-synonym: "The elemental composition should be assumed incorrect" RELATED []
-xref: record_id "1974"
-xref: delta_mono_mass "234.073953"
-xref: delta_avge_mass "234.2033"
-xref: delta_composition "H(14) C(9) O(7)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-12-07 10:00:16"
-xref: date_time_modified "2017-12-07 10:00:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1975
-name: Unknown:248
-def: "Unidentified modification of 248.1986 found in open search." [URL:http\://www.matrixscience.com/blog/trying-to-illuminate-proteomics-dark-matter.html, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1975]
-synonym: "The elemental composition should be assumed incorrect" RELATED []
-xref: record_id "1975"
-xref: delta_mono_mass "248.19876"
-xref: delta_avge_mass "248.359"
-xref: delta_composition "H(28) C(13) O(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-12-07 10:00:57"
-xref: date_time_modified "2017-12-07 10:00:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1976
-name: Unknown:250
-def: "Unidentified modification of 249.981 found in open search." [URL:http\://www.matrixscience.com/blog/trying-to-illuminate-proteomics-dark-matter.html, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1976]
-synonym: "The elemental composition should be assumed incorrect" RELATED []
-xref: record_id "1976"
-xref: delta_mono_mass "249.981018"
-xref: delta_avge_mass "250.2075"
-xref: delta_composition "H(4) C(10) N O(5) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-12-07 10:01:43"
-xref: date_time_modified "2017-12-07 10:01:43"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1977
-name: Unknown:302
-def: "Unidentified modification of 301.9864 found in open search." [URL:http\://www.matrixscience.com/blog/trying-to-illuminate-proteomics-dark-matter.html, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1977]
-synonym: "The elemental composition should be assumed incorrect" RELATED []
-xref: record_id "1977"
-xref: delta_mono_mass "301.986514"
-xref: delta_avge_mass "302.2656"
-xref: delta_composition "H(8) C(4) N(5) O(7) S(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-12-07 10:02:16"
-xref: date_time_modified "2017-12-07 10:02:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1978
-name: Unknown:306
-def: "Unidentified modification of 306.0952 found in open search." [URL:http\://www.matrixscience.com/blog/trying-to-illuminate-proteomics-dark-matter.html, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1978]
-synonym: "The elemental composition should be assumed incorrect" RELATED []
-xref: record_id "1978"
-xref: delta_mono_mass "306.095082"
-xref: delta_avge_mass "306.2659"
-xref: delta_composition "H(18) C(12) O(9)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-12-07 10:03:12"
-xref: date_time_modified "2017-12-07 10:03:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1979
-name: Unknown:420
-def: "Unidentified modification of 420.0506 found in open search." [URL:http\://www.matrixscience.com/blog/results-round-up-for-the-dark-matter-challenge.html, URL:http\://www.matrixscience.com/blog/trying-to-illuminate-proteomics-dark-matter.html, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1979]
-synonym: "Probable non-covalent adduct of CAM-DTT-DTT-CAM" RELATED []
-xref: record_id "1979"
-xref: delta_mono_mass "420.051719"
-xref: delta_avge_mass "420.5888"
-xref: delta_composition "H(24) C(12) N(2) O(6) S(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-12-07 10:03:58"
-xref: date_time_modified "2019-10-17 16:01:58"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Any C-term"
-xref: spec_1_classification "Artefact"
-xref: spec_1_neutral_loss_421_mono_mass "420.051719"
-xref: spec_1_neutral_loss_421_avge_mass "420.5888"
-xref: spec_1_neutral_loss_421_flag "false"
-xref: spec_1_neutral_loss_421_composition "H(24) C(12) N(2) O(6) S(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Artefact"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_421_mono_mass "420.051719"
-xref: spec_2_neutral_loss_421_avge_mass "420.5888"
-xref: spec_2_neutral_loss_421_flag "false"
-xref: spec_2_neutral_loss_421_composition "H(24) C(12) N(2) O(6) S(4)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1986
-name: Diethylphosphothione
-def: "O-diethylphosphothione." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1986]
-xref: record_id "1986"
-xref: delta_mono_mass "152.006087"
-xref: delta_avge_mass "152.1518"
-xref: delta_composition "H(9) C(4) O(2) P S"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2018-03-04 15:26:03"
-xref: date_time_modified "2018-03-08 13:03:26"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "S"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "T"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "Y"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1987
-name: Dimethylphosphothione
-def: "O-dimethylphosphothione." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1987]
-synonym: "O-ethylphosphothione" RELATED []
-xref: record_id "1987"
-xref: delta_mono_mass "123.974787"
-xref: delta_avge_mass "124.0987"
-xref: delta_composition "H(5) C(2) O(2) P S"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2018-03-04 15:31:14"
-xref: date_time_modified "2018-03-08 13:02:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "S"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "T"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "Y"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1989
-name: monomethylphosphothione
-def: "O-methylphosphothione." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1989]
-comment: Created by auto-catalytic dealkylation of the O-dimethylphosphothione adduct.
-xref: record_id "1989"
-xref: delta_mono_mass "109.959137"
-xref: delta_avge_mass "110.0721"
-xref: delta_composition "H(3) C O(2) P S"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2018-03-04 16:13:58"
-xref: date_time_modified "2018-03-08 13:04:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "S"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "T"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "Y"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1990
-name: CIGG
-def: "Ubiquitin D (FAT10) leaving after chymotrypsin digestion Cys-Ile-Gly-Gly." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1990]
-xref: record_id "1990"
-xref: delta_mono_mass "330.136176"
-xref: delta_avge_mass "330.4032"
-xref: delta_composition "H(22) C(13) N(4) O(4) S"
-xref: username_of_poster "cosmoguidry"
-xref: group_of_poster ""
-xref: date_time_posted "2018-03-13 12:00:08"
-xref: date_time_modified "2018-03-16 10:22:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1991
-name: GNLLFLACYCIGG
-def: "Ubiquitin D (FAT10) leaving after trypsin digestion Gly-Asn-Leu-Leu-Phe-Leu-Ala-Cys-Tyr-Cys-Ile-Gly-Gly." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1991]
-xref: record_id "1991"
-xref: delta_mono_mass "1324.6308"
-xref: delta_avge_mass "1325.598"
-xref: delta_composition "H(92) C(61) N(14) O(15) S(2)"
-xref: username_of_poster "cosmoguidry"
-xref: group_of_poster ""
-xref: date_time_posted "2018-03-15 15:07:14"
-xref: date_time_modified "2018-03-16 10:21:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1992
-name: serotonylation
-def: "5-glutamyl serotonin." [RESID:AA0528, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1992]
-xref: record_id "1992"
-xref: delta_mono_mass "159.068414"
-xref: delta_avge_mass "159.1846"
-xref: delta_composition "H(9) C(10) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2018-04-17 09:27:35"
-xref: date_time_modified "2018-04-17 09:27:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1993
-name: TMPP-Ac:13C(9)
-def: "Heavy tris(2,4,6-trimethoxyphenyl)phosphonium acetic acid N-hydroxysuccinimide ester derivative." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1993]
-comment: The formula is reduced from H(34) to H(33) so as to give correct observed m/z values. The charge on the TMPP means that ions have one less proton than would be expected.
-xref: record_id "1993"
-xref: delta_mono_mass "581.211328"
-xref: delta_avge_mass "581.474"
-xref: delta_composition "H(33) C(20) 13C(9) O(10) P"
-xref: username_of_poster "rompais"
-xref: group_of_poster ""
-xref: date_time_posted "2018-06-26 13:54:23"
-xref: date_time_modified "2018-06-26 15:21:14"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Artefact"
-xref: spec_2_misc_notes "possible side chain reaction when labeling N-term"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Artefact"
-xref: spec_3_misc_notes "possible side chain reaction when labeling N-term"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1999
-name: Xlink:DST[56]
-def: "DST crosslinker cleaved by sodium periodate." [URL:https\://assets.thermofisher.com/TFS-Assets/LSG/manuals/MAN0011282_DST_UG.pdf, PMID:212103, PMID:3001048, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1999]
-xref: record_id "1999"
-xref: delta_mono_mass "55.989829"
-xref: delta_avge_mass "56.0202"
-xref: delta_composition "C(2) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2018-08-29 11:31:26"
-xref: date_time_modified "2018-08-29 11:37:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2001
-name: ZQG
-def: "Carbobenzoxy-L-glutaminyl-glycine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2001]
-comment: Glutamine-donor substrate for transglutaminase.
-xref: record_id "2001"
-xref: delta_mono_mass "320.100836"
-xref: delta_avge_mass "320.2973"
-xref: delta_composition "H(16) C(15) N(2) O(6)"
-xref: username_of_poster "Barbara Spolaore"
-xref: group_of_poster ""
-xref: date_time_posted "2018-09-18 12:01:47"
-xref: date_time_modified "2019-06-05 10:18:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_neutral_loss_135_mono_mass "134.036779"
-xref: spec_1_neutral_loss_135_avge_mass "134.132"
-xref: spec_1_neutral_loss_135_flag "false"
-xref: spec_1_neutral_loss_135_composition "H(6) C(8) O(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2006
-name: Haloxon
-def: "O-Dichloroethylphosphate." [PMID:4677141, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2006]
-xref: record_id "2006"
-xref: delta_mono_mass "203.950987"
-xref: delta_avge_mass "204.9763"
-xref: delta_composition "H(7) C(4) O(3) P Cl(2)"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2019-03-21 14:40:01"
-xref: date_time_modified "2019-03-21 15:45:39"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "T"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "S"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "Y"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2007
-name: Methamidophos-S
-def: "S-methyl amino phosphinate." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2007]
-xref: record_id "2007"
-xref: delta_mono_mass "108.975121"
-xref: delta_avge_mass "109.0873"
-xref: delta_composition "H(4) C N O P S"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2019-03-22 16:54:28"
-xref: date_time_modified "2019-05-22 14:56:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "S"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "T"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "Y"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2008
-name: Methamidophos-O
-def: "O-methyl amino phosphinate." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2008]
-xref: record_id "2008"
-xref: delta_mono_mass "92.997965"
-xref: delta_avge_mass "93.0217"
-xref: delta_composition "H(4) C N O(2) P"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2019-03-22 17:03:48"
-xref: date_time_modified "2019-05-22 14:57:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "S"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "T"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "Y"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2014
-name: Nitrene
-def: "Loss of O2; nitro photochemical decomposition." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2014]
-xref: record_id "2014"
-xref: delta_mono_mass "12.995249"
-xref: delta_avge_mass "12.9988"
-xref: delta_composition "H(-1) N"
-xref: username_of_poster "alhansen"
-xref: group_of_poster ""
-xref: date_time_posted "2019-07-10 21:24:33"
-xref: date_time_modified "2019-09-10 09:30:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2015
-name: shTMT
-def: "Super Heavy Tandem Mass Tag." [URL:https\://www.thermofisher.com/order/catalog/product/A43073, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2015]
-comment: This modification describes the Super Heavy TMT Reagent. Upon HCD, this reagent releases a reporter ion of 132.14153 (monoisotopic mass).
-synonym: "Tandem Mass Tag and TMT are registered Trademarks of Proteome Sciences plc. Super Heavy TMT" RELATED []
-xref: record_id "2015"
-xref: delta_mono_mass "235.176741"
-xref: delta_avge_mass "235.2201"
-xref: delta_composition "H(20) C(3) 13C(9) 15N(2) O(2)"
-xref: username_of_poster "rbomgard"
-xref: group_of_poster ""
-xref: date_time_posted "2019-07-10 21:42:41"
-xref: date_time_modified "2019-09-10 09:30:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2016
-name: TMTpro
-def: "TMTpro 16plex Tandem Mass Tag." [URL:https\://www.thermofisher.com/order/catalog/product/A44520, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2016]
-comment: This modification describes the isotope-labeled TMTpro Reagent with m/z values of the TMTpro fragment ions to be quantified for 16plex: 126.127726,127. 124761, 127.131081, 128.128116, 128.134436, 129.131471, 129.13779, 130.134825, 130.141145, 131.13818, 131.1445, 132.141535, 132.147855, 133.14489, 133.15121, and 134.148245 Additional reporter ions for 18plex: 134.154565 and 135.151600.
-synonym: "Tandem Mass Tag and TMT are registered Trademarks of Proteome Sciences plc. Also applies to TMTpro 18plex mass tags" RELATED []
-xref: record_id "2016"
-xref: delta_mono_mass "304.207146"
-xref: delta_avge_mass "304.3127"
-xref: delta_composition "H(25) C(8) 13C(7) N 15N(2) O(3)"
-xref: username_of_poster "rbomgard"
-xref: group_of_poster ""
-xref: date_time_posted "2019-09-06 19:43:32"
-xref: date_time_modified "2021-07-22 21:42:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Isotopic label"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "H"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "S"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Isotopic label"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "T"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2017
-name: TMTpro_zero
-def: "Native TMTpro Tandem Mass Tag." [URL:https\://www.thermofisher.com/order/catalog/product/A44518, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2017]
-comment: This modification describes the native TMTpro Reagent without isotopic label with reporter mass m/z 126.127726.
-synonym: "Tandem Mass Tag and TMT are registered Trademarks of Proteome Sciences plc." RELATED []
-xref: record_id "2017"
-xref: delta_mono_mass "295.189592"
-xref: delta_avge_mass "295.3773"
-xref: delta_composition "H(25) C(15) N(3) O(3)"
-xref: username_of_poster "rbomgard"
-xref: group_of_poster ""
-xref: date_time_posted "2019-09-06 20:04:30"
-xref: date_time_modified "2019-09-10 09:10:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "H"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "S"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "T"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2022
-name: Ser/Thr-KDO
-def: "Glycosylation of Serine/Threonine residues with KDO." [PMID:https://books.google.co.in/books?id=IOuPDwAAQBAJ&pg=PA333&lpg=PA333&dq=kdo+220+mass&source=bl&ots=t--BcUkzNH&sig=ACfU3U2lNj05UnTthH1BD6fS0jC6rxYpFw&hl=en&sa=X&ved=2ahUKEwjLmPfoic7nAhWA7XMBHRsiAk4Q6AEwCnoECAoQAQ#v=onepage&q=kdo%20220%20mass&f=false, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2022]
-synonym: "3-deoxy-D-manno-oct-2-ulosonic acid 2-Keto-3-Deoxy-D-Mannooctanoic Acid" RELATED []
-xref: record_id "2022"
-xref: delta_mono_mass "220.058303"
-xref: delta_avge_mass "220.1767"
-xref: delta_composition "H(12) C(8) O(7)"
-xref: username_of_poster "ramya"
-xref: group_of_poster ""
-xref: date_time_posted "2020-02-13 12:07:17"
-xref: date_time_modified "2022-10-20 12:17:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_221_mono_mass "220.058303"
-xref: spec_1_neutral_loss_221_avge_mass "220.1767"
-xref: spec_1_neutral_loss_221_flag "false"
-xref: spec_1_neutral_loss_221_composition "H(12) C(8) O(7)"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_221_mono_mass "220.058303"
-xref: spec_1_neutral_loss_221_avge_mass "220.1767"
-xref: spec_1_neutral_loss_221_flag "false"
-xref: spec_1_neutral_loss_221_composition "H(12) C(8) O(7)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2025
-name: Andro-H2O
-def: "Andrographolide with the loss of H2O." [PMID:24445406, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2025]
-xref: record_id "2025"
-xref: delta_mono_mass "332.19876"
-xref: delta_avge_mass "332.4339"
-xref: delta_composition "H(28) C(20) O(4)"
-xref: username_of_poster "nekoooooo"
-xref: group_of_poster ""
-xref: date_time_posted "2020-05-18 08:48:39"
-xref: date_time_modified "2020-05-26 15:47:33"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2027
-name: His+O(2)
-def: "Photo-induced histidine adduct." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2027]
-xref: record_id "2027"
-xref: delta_mono_mass "169.048741"
-xref: delta_avge_mass "169.1381"
-xref: delta_composition "H(7) C(6) N(3) O(3)"
-xref: username_of_poster "tomp1808"
-xref: group_of_poster ""
-xref: date_time_posted "2020-06-01 16:45:37"
-xref: date_time_modified "2020-06-09 11:01:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2028
-name: Hex(6)HexNAc(5)NeuAc(3)
-def: "A3G3S3." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=6&hexnac=5&neuac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2028]
-xref: record_id "2028"
-xref: delta_mono_mass "2861.000054"
-xref: delta_avge_mass "2862.5699"
-xref: delta_composition "Hex(6) HexNAc(5) NeuAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2020-08-02 11:44:31"
-xref: date_time_modified "2020-08-02 11:44:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_2862_mono_mass "2861.000054"
-xref: spec_1_neutral_loss_2862_avge_mass "2862.5699"
-xref: spec_1_neutral_loss_2862_flag "false"
-xref: spec_1_neutral_loss_2862_composition "Hex(6) HexNAc(5) NeuAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2029
-name: Hex(7)HexNAc(6)
-def: "A4G4." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=7&hexnac=6&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2029]
-xref: record_id "2029"
-xref: delta_mono_mass "2352.846"
-xref: delta_avge_mass "2354.1393"
-xref: delta_composition "Hex(7) HexNAc(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2020-08-02 11:47:40"
-xref: date_time_modified "2020-08-02 11:47:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_2353_mono_mass "2352.846"
-xref: spec_1_neutral_loss_2353_avge_mass "2354.1393"
-xref: spec_1_neutral_loss_2353_flag "false"
-xref: spec_1_neutral_loss_2353_composition "Hex(7) HexNAc(6)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_2353_mono_mass "2352.846"
-xref: spec_1_neutral_loss_2353_avge_mass "2354.1393"
-xref: spec_1_neutral_loss_2353_flag "false"
-xref: spec_1_neutral_loss_2353_composition "Hex(7) HexNAc(6)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_2353_mono_mass "2352.846"
-xref: spec_2_neutral_loss_2353_avge_mass "2354.1393"
-xref: spec_2_neutral_loss_2353_flag "false"
-xref: spec_2_neutral_loss_2353_composition "Hex(7) HexNAc(6)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2033
-name: Met+O(2)
-def: "Photo-induced Methionine Adduct." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2033]
-xref: record_id "2033"
-xref: delta_mono_mass "163.030314"
-xref: delta_avge_mass "163.1949"
-xref: delta_composition "H(9) C(5) N O(3) S"
-xref: username_of_poster "tomp1808"
-xref: group_of_poster ""
-xref: date_time_posted "2021-02-01 10:35:58"
-xref: date_time_modified "2021-03-09 13:26:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "Oxidative cross-link of free methionine to histidine residue in protein."
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2034
-name: Gly+O(2)
-def: "Photo-induced Glycine Adduct." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2034]
-xref: record_id "2034"
-xref: delta_mono_mass "89.011293"
-xref: delta_avge_mass "89.0501"
-xref: delta_composition "H(3) C(2) N O(3)"
-xref: username_of_poster "tomp1808"
-xref: group_of_poster ""
-xref: date_time_posted "2021-02-01 13:18:42"
-xref: date_time_modified "2021-03-09 13:27:33"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2035
-name: Pro+O(2)
-def: "Photo-induced Proline adduct." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2035]
-xref: record_id "2035"
-xref: delta_mono_mass "129.042593"
-xref: delta_avge_mass "129.114"
-xref: delta_composition "H(7) C(5) N O(3)"
-xref: username_of_poster "tomp1808"
-xref: group_of_poster ""
-xref: date_time_posted "2021-02-01 13:30:11"
-xref: date_time_modified "2021-03-09 13:28:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2036
-name: Lys+O(2)
-def: "Photo-induced Lysine adduct." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2036]
-xref: record_id "2036"
-xref: delta_mono_mass "160.084792"
-xref: delta_avge_mass "160.1711"
-xref: delta_composition "H(12) C(6) N(2) O(3)"
-xref: username_of_poster "tomp1808"
-xref: group_of_poster ""
-xref: date_time_posted "2021-02-01 13:33:53"
-xref: date_time_modified "2021-03-09 13:28:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2037
-name: Glu+O(2)
-def: "Photo-induced Glutamate adduct." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2037]
-xref: record_id "2037"
-xref: delta_mono_mass "161.032422"
-xref: delta_avge_mass "161.1128"
-xref: delta_composition "H(7) C(5) N O(5)"
-xref: username_of_poster "tomp1808"
-xref: group_of_poster ""
-xref: date_time_posted "2021-02-01 13:35:06"
-xref: date_time_modified "2021-03-09 13:28:59"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2039
-name: LTX+Lophotoxin
-def: "Addition of lophotoxin to tyrosine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2039]
-xref: record_id "2039"
-xref: delta_mono_mass "416.147118"
-xref: delta_avge_mass "416.4212"
-xref: delta_composition "H(24) C(22) O(8)"
-xref: username_of_poster "modchaser99"
-xref: group_of_poster ""
-xref: date_time_posted "2021-02-17 23:23:43"
-xref: date_time_modified "2021-03-09 13:32:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2040
-name: MBS+peptide
-def: "MBS_233p24 plus peptide 1250p53." [URL:https\://www.thermofisher.com/order/catalog/product/22311?us&en#/22311?us&en, PMID:https://pubmed.ncbi.nlm.nih.gov/8829804/, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2040]
-xref: record_id "2040"
-xref: delta_mono_mass "1482.77"
-xref: delta_avge_mass "1483.7597"
-xref: delta_composition "H(108) C(81) N(7) O(19)"
-xref: username_of_poster "nendicott"
-xref: group_of_poster ""
-xref: date_time_posted "2021-02-24 17:50:09"
-xref: date_time_modified "2021-03-09 13:32:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "Loss of MBS, peptide from KLH after trypsin digestion"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2041
-name: 3-hydroxybenzyl-phosphate
-def: "3-hydroxybenzyl phosphate." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2041]
-comment: Created by hydrolysis of the product of the reaction of 2-(o-cresyl)-4H-1,3,2-benzodioxaphosphorane-2-one with amino acids residues in proteins.
-xref: record_id "2041"
-xref: delta_mono_mass "186.008196"
-xref: delta_avge_mass "186.1018"
-xref: delta_composition "H(7) C(7) O(4) P"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2021-03-07 21:17:23"
-xref: date_time_modified "2021-03-09 13:34:53"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "Y"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2042
-name: phenyl-phosphate
-def: "Phenyl phosphate." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2042]
-comment: Created by hydrolysis of the product of the reaction of 2-(o-cresyl)-4H-1,3,2-benzodioxaphosphorane-2-one with amino acids residues in proteins.
-xref: record_id "2042"
-xref: delta_mono_mass "155.997631"
-xref: delta_avge_mass "156.0759"
-xref: delta_composition "H(5) C(6) O(3) P"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2021-03-07 21:23:37"
-xref: date_time_modified "2021-03-09 13:36:06"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "Y"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2044
-name: RBS-ID_Uridine
-def: "RNA-protein UVC-crosslinked, hydrofluoride-digested uridine adduct." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2044]
-xref: record_id "2044"
-xref: delta_mono_mass "244.069536"
-xref: delta_avge_mass "244.2014"
-xref: delta_composition "H(12) C(9) N(2) O(6)"
-xref: username_of_poster "jwbaebio"
-xref: group_of_poster ""
-xref: date_time_posted "2021-06-02 01:11:04"
-xref: date_time_modified "2021-11-20 23:24:33"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_1_misc_notes "Crosslink to all 20 amino acids. Not C-term (Missed cleavage). Partial in-source fragmentation to Uracil (loss of ribose): H(4) C(4) N(2) O(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2050
-name: shTMTpro
-def: "Super Heavy TMTpro." [URL:https\://www.thermofisher.com/order/catalog/product/A52040, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2050]
-comment: This modification describes the Super Heavy TMTpro Reagent. Upon HCD, this reagent releases a reporter ion of 135.151600 (monoisotopic mass).
-synonym: "Tandem Mass Tag and TMT are registered Trademarks of Proteome Sciences plc. TMTpro-SH 13C15 H25 15N3 O3" RELATED []
-xref: record_id "2050"
-xref: delta_mono_mass "313.231019"
-xref: delta_avge_mass "313.2473"
-xref: delta_composition "H(25) 13C(15) 15N(3) O(3)"
-xref: username_of_poster "rbomgard"
-xref: group_of_poster ""
-xref: date_time_posted "2021-07-22 21:45:43"
-xref: date_time_modified "2021-07-22 21:45:43"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2052
-name: Biotin:Aha-DADPS
-def: "Intact DADPS Biotin Alkyne tag." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2052]
-comment: Methionine is substituted in culture with azidohomoalanine. The azide group reacts with the alkyne group of DADPS Biotin Alkyne.
-xref: record_id "2052"
-xref: delta_mono_mass "922.465403"
-xref: delta_avge_mass "923.2022"
-xref: delta_composition "H(70) C(42) N(8) O(11) Si S"
-xref: username_of_poster "pluck"
-xref: group_of_poster ""
-xref: date_time_posted "2021-07-28 08:57:58"
-xref: date_time_modified "2021-07-28 09:44:43"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2053
-name: Biotin:Aha-PC
-def: "Intact PC Biotin Alkyne tag." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2053]
-comment: Methionine is substituted in culture with azidohomoalanine. The azide group reacts with the alkyne group of PC Biotin Alkyne.
-xref: record_id "2053"
-xref: delta_mono_mass "690.24316"
-xref: delta_avge_mass "690.7246"
-xref: delta_composition "H(38) C(29) N(8) O(10) S"
-xref: username_of_poster "pluck"
-xref: group_of_poster ""
-xref: date_time_posted "2021-09-30 07:29:58"
-xref: date_time_modified "2021-09-30 07:43:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2054
-name: pRBS-ID_4-thiouridine
-def: "RNA-protein UVA-crosslinked, hydrofluoride-digested 4-thiouridine adduct." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2054]
-xref: record_id "2054"
-xref: delta_mono_mass "226.058972"
-xref: delta_avge_mass "226.1861"
-xref: delta_composition "H(10) C(9) N(2) O(5)"
-xref: username_of_poster "jwbaebio"
-xref: group_of_poster ""
-xref: date_time_posted "2021-10-16 02:47:03"
-xref: date_time_modified "2022-01-10 11:09:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_1_misc_notes "Crosslink to all 20 amino acids. Not C-term (Missed cleavage). Partial in-source fragmentation & near-complete HCD-mediated fragmentation to 4-thiouracil form: H(2) C(4) N(2) O(1)"
-xref: spec_1_neutral_loss_133_mono_mass "132.042259"
-xref: spec_1_neutral_loss_133_avge_mass "132.1146"
-xref: spec_1_neutral_loss_133_flag "false"
-xref: spec_1_neutral_loss_133_composition "H(8) C(5) O(4)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2055
-name: pRBS-ID_6-thioguanosine
-def: "RNA-protein UVA-crosslinked, hydrofluoride-digested 6-thioguanosine adduct." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2055]
-xref: record_id "2055"
-xref: delta_mono_mass "265.081104"
-xref: delta_avge_mass "265.2254"
-xref: delta_composition "H(11) C(10) N(5) O(4)"
-xref: username_of_poster "jwbaebio"
-xref: group_of_poster ""
-xref: date_time_posted "2021-10-16 02:54:01"
-xref: date_time_modified "2022-01-10 11:08:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_1_misc_notes "Crosslink to all 20 amino acids. Not C-term (Missed cleavage). Partial in-source fragmentation & near-complete HCD-mediated fragmentation to 6-thioguanine form: H(3) C(5) N(5)"
-xref: spec_1_neutral_loss_133_mono_mass "132.042259"
-xref: spec_1_neutral_loss_133_avge_mass "132.1146"
-xref: spec_1_neutral_loss_133_flag "false"
-xref: spec_1_neutral_loss_133_composition "H(8) C(5) O(4)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2057
-name: 6C-CysPAT
-def: "Iodoacetamido-LC-Phosphonic Acid derivative." [PMID:32109415, URL:https\://www.thermofisher.com/order/catalog/product/A52285, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2057]
-synonym: "Carbamido-LC-phosphoyrlation A52285" RELATED []
-xref: record_id "2057"
-xref: delta_mono_mass "221.081695"
-xref: delta_avge_mass "221.1907"
-xref: delta_composition "H(16) C(8) N O(4) P"
-xref: username_of_poster "rbomgard"
-xref: group_of_poster ""
-xref: date_time_posted "2022-01-06 21:30:30"
-xref: date_time_modified "2022-01-07 19:11:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "0"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Artefact"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "H"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Artefact"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "D"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Artefact"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "E"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Artefact"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "S"
-xref: spec_7_position "Anywhere"
-xref: spec_7_classification "Artefact"
-xref: spec_8_group "8"
-xref: spec_8_hidden "1"
-xref: spec_8_site "T"
-xref: spec_8_position "Anywhere"
-xref: spec_8_classification "Artefact"
-xref: spec_9_group "9"
-xref: spec_9_hidden "1"
-xref: spec_9_site "Y"
-xref: spec_9_position "Anywhere"
-xref: spec_9_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2058
-name: Xlink:DSPP[210]
-def: "Intact DSPP/TBDSPP crosslinker." [PMID:31572778, URL:https\://www.thermofisher.com/order/catalog/product/A52286, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2058]
-synonym: "PhoX, tBu-PhoX (acid deprotected) A52286, A52287" RELATED []
-xref: record_id "2058"
-xref: delta_mono_mass "209.97181"
-xref: delta_avge_mass "210.0802"
-xref: delta_composition "H(3) C(8) O(5) P"
-xref: username_of_poster "rbomgard"
-xref: group_of_poster ""
-xref: date_time_posted "2022-01-06 21:47:14"
-xref: date_time_modified "2022-01-06 21:52:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2059
-name: Xlink:DSPP[228]
-def: "Water-quenched monolink of DSPP/TBDSPP crosslinker." [URL:https\://www.thermofisher.com/order/catalog/product/A52286, PMID:31572778, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2059]
-synonym: "A52286, A52287 PhoX, tBu-PhoX (acid deprotected) water quench" RELATED []
-xref: record_id "2059"
-xref: delta_mono_mass "227.982375"
-xref: delta_avge_mass "228.0955"
-xref: delta_composition "H(5) C(8) O(6) P"
-xref: username_of_poster "rbomgard"
-xref: group_of_poster ""
-xref: date_time_posted "2022-01-06 21:55:27"
-xref: date_time_modified "2022-01-06 21:57:32"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2060
-name: Xlink:DSPP[331]
-def: "Tris-quenched monolink of DSPP/TBDSPP crosslinker." [URL:https\://www.thermofisher.com/order/catalog/product/A52286, PMID:31572778, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2060]
-synonym: "C12 H14 N O8 P PhoX, tBu-PhoX (acid deprotected) Tris quench A52286, A52287" RELATED []
-xref: record_id "2060"
-xref: delta_mono_mass "331.045704"
-xref: delta_avge_mass "331.2152"
-xref: delta_composition "H(14) C(12) N O(8) P"
-xref: username_of_poster "rbomgard"
-xref: group_of_poster ""
-xref: date_time_posted "2022-01-06 22:01:09"
-xref: date_time_modified "2022-01-06 22:06:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2061
-name: Xlink:DSPP[226]
-def: "Ammonia-quenched monolink of DSPP/TBDSPP crosslinker." [URL:https\://www.thermofisher.com/order/catalog/product/A52286, PMID:31572778, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2061]
-synonym: "PhoX, tBu-PhoX (acid deprotected) ammonia quench A52286, A52287" RELATED []
-xref: record_id "2061"
-xref: delta_mono_mass "225.990534"
-xref: delta_avge_mass "226.1028"
-xref: delta_composition "H(5) C(8) N O(5) P"
-xref: username_of_poster "rbomgard"
-xref: group_of_poster ""
-xref: date_time_posted "2022-01-06 22:04:48"
-xref: date_time_modified "2022-01-07 19:13:43"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2062
-name: DBIA
-def: "Desthiobiotinylation of cysteine with DBIA probe." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2062]
-xref: record_id "2062"
-xref: delta_mono_mass "296.184841"
-xref: delta_avge_mass "296.3654"
-xref: delta_composition "H(24) C(14) N(4) O(3)"
-xref: username_of_poster "amz281"
-xref: group_of_poster ""
-xref: date_time_posted "2022-03-09 14:56:17"
-xref: date_time_modified "2022-04-18 11:09:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2067
-name: Mono_Ngamma-propargyl-L-Gln_desthiobiotin
-def: "Monomodification of Ngamma-propargyl-L-Gln probe with clicked desthiobiotin-azide." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2067]
-comment: - desthiobiotin-azide to enrich L-Gln-propargyl modified peptides.
-synonym: "Enrichment of modified peptides using desthiobiotin-tag on streptavidin beads" RELATED []
-xref: record_id "2067"
-xref: delta_mono_mass "596.328211"
-xref: delta_avge_mass "596.6764"
-xref: delta_composition "H(44) C(26) N(8) O(8)"
-xref: username_of_poster "KielkowskiLab"
-xref: group_of_poster ""
-xref: date_time_posted "2022-08-05 13:31:40"
-xref: date_time_modified "2024-08-12 11:07:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2068
-name: Di_L-Glu_Ngamma-propargyl-L-Gln_desthiobiotin
-def: "Dimodification of L-Glu and Ngamma-propargyl-L-Gln probe with clicked desthiobiotin-azide." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2068]
-comment: - desthiobiotin-azide to enrich L-Gln-propargyl modified peptides.
-xref: record_id "2068"
-xref: delta_mono_mass "709.375889"
-xref: delta_avge_mass "709.7909"
-xref: delta_composition "H(51) C(31) N(9) O(10)"
-xref: username_of_poster "KielkowskiLab"
-xref: group_of_poster ""
-xref: date_time_posted "2022-08-09 13:38:45"
-xref: date_time_modified "2024-08-12 11:06:43"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_neutral_loss_197_mono_mass "196.121178"
-xref: spec_1_neutral_loss_197_avge_mass "196.2462"
-xref: spec_1_neutral_loss_197_flag "false"
-xref: spec_1_neutral_loss_197_composition "H(16) C(10) N(2) O(2)"
-xref: spec_1_neutral_loss_728_mono_mass "727.386454"
-xref: spec_1_neutral_loss_728_avge_mass "727.8062"
-xref: spec_1_neutral_loss_728_flag "false"
-xref: spec_1_neutral_loss_728_composition "H(53) C(31) N(9) O(11)"
-xref: spec_1_neutral_loss_470_mono_mass "469.301268"
-xref: spec_1_neutral_loss_470_avge_mass "469.5783"
-xref: spec_1_neutral_loss_470_flag "false"
-xref: spec_1_neutral_loss_470_composition "H(39) C(21) N(7) O(5)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "E"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_2_neutral_loss_197_mono_mass "196.121178"
-xref: spec_2_neutral_loss_197_avge_mass "196.2462"
-xref: spec_2_neutral_loss_197_flag "false"
-xref: spec_2_neutral_loss_197_composition "H(16) C(10) N(2) O(2)"
-xref: spec_2_neutral_loss_470_mono_mass "469.301268"
-xref: spec_2_neutral_loss_470_avge_mass "469.5783"
-xref: spec_2_neutral_loss_470_flag "false"
-xref: spec_2_neutral_loss_470_composition "H(39) C(21) N(7) O(5)"
-xref: spec_2_neutral_loss_728_mono_mass "727.386454"
-xref: spec_2_neutral_loss_728_avge_mass "727.8062"
-xref: spec_2_neutral_loss_728_flag "false"
-xref: spec_2_neutral_loss_728_composition "H(53) C(31) N(9) O(11)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2069
-name: Di_L-Gln_Ngamma-propargyl-L-Gln_desthiobiotin
-def: "Dimodification of L-Gln and Ngamma-propargyl-L-Gln probe with clicked desthiobiotin-azide." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2069]
-comment: - desthiobiotin-azide to enrich L-Gln-propargyl modified peptides.
-xref: record_id "2069"
-xref: delta_mono_mass "708.391873"
-xref: delta_avge_mass "708.8062"
-xref: delta_composition "H(52) C(31) N(10) O(9)"
-xref: username_of_poster "KielkowskiLab"
-xref: group_of_poster ""
-xref: date_time_posted "2022-08-09 13:45:33"
-xref: date_time_modified "2024-08-12 11:06:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_neutral_loss_197_mono_mass "196.121178"
-xref: spec_1_neutral_loss_197_avge_mass "196.2462"
-xref: spec_1_neutral_loss_197_flag "false"
-xref: spec_1_neutral_loss_197_composition "H(16) C(10) N(2) O(2)"
-xref: spec_1_neutral_loss_727_mono_mass "726.402438"
-xref: spec_1_neutral_loss_727_avge_mass "726.8215"
-xref: spec_1_neutral_loss_727_flag "false"
-xref: spec_1_neutral_loss_727_composition "H(54) C(31) N(10) O(10)"
-xref: spec_1_neutral_loss_470_mono_mass "469.301268"
-xref: spec_1_neutral_loss_470_avge_mass "469.5783"
-xref: spec_1_neutral_loss_470_flag "false"
-xref: spec_1_neutral_loss_470_composition "H(39) C(21) N(7) O(5)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "E"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_2_neutral_loss_727_mono_mass "726.402438"
-xref: spec_2_neutral_loss_727_avge_mass "726.8215"
-xref: spec_2_neutral_loss_727_flag "false"
-xref: spec_2_neutral_loss_727_composition "H(54) C(31) N(10) O(10)"
-xref: spec_2_neutral_loss_470_mono_mass "469.301268"
-xref: spec_2_neutral_loss_470_avge_mass "469.5783"
-xref: spec_2_neutral_loss_470_flag "false"
-xref: spec_2_neutral_loss_470_composition "H(39) C(21) N(7) O(5)"
-xref: spec_2_neutral_loss_197_mono_mass "196.121178"
-xref: spec_2_neutral_loss_197_avge_mass "196.2462"
-xref: spec_2_neutral_loss_197_flag "false"
-xref: spec_2_neutral_loss_197_composition "H(16) C(10) N(2) O(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2070
-name: L-Gln
-def: "Monomodification with glutamine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2070]
-xref: record_id "2070"
-xref: delta_mono_mass "128.058578"
-xref: delta_avge_mass "128.1292"
-xref: delta_composition "H(8) C(5) N(2) O(2)"
-xref: username_of_poster "KielkowskiLab"
-xref: group_of_poster ""
-xref: date_time_posted "2022-08-25 13:15:56"
-xref: date_time_modified "2022-10-20 14:06:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "D"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2072
-name: Glyceroyl
-def: "Glyceroylation." [PMID:35046029, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2072]
-xref: record_id "2072"
-xref: delta_mono_mass "88.016044"
-xref: delta_avge_mass "88.0621"
-xref: delta_composition "H(4) C(3) O(3)"
-xref: username_of_poster "heremans"
-xref: group_of_poster ""
-xref: date_time_posted "2022-09-06 09:03:01"
-xref: date_time_modified "2022-10-20 14:05:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2073
-name: N6pAMP
-def: "Plain N6-Propargyl-AMP modified proteins without any clicked enrichment tag." [PMID:21942216, PMID:31980631, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2073]
-xref: record_id "2073"
-xref: delta_mono_mass "367.06817"
-xref: delta_avge_mass "367.2539"
-xref: delta_composition "H(14) C(13) N(5) O(6) P"
-xref: username_of_poster "KielkowskiLab"
-xref: group_of_poster ""
-xref: date_time_posted "2023-02-06 14:36:27"
-xref: date_time_modified "2023-10-05 14:38:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2074
-name: DABCYL-C2-maleimide
-def: "DABCYL-C2-maleimide Thiol-reactive dye for fluorescence labelling of proteins." [PMID:25197743, URL:https\://www.aatbio.com/products/dabcyl-c2-maleimide, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2074]
-xref: record_id "2074"
-xref: delta_mono_mass "391.16444"
-xref: delta_avge_mass "391.4231"
-xref: delta_composition "H(21) C(21) N(5) O(3)"
-xref: username_of_poster "amedalin"
-xref: group_of_poster ""
-xref: date_time_posted "2023-02-15 13:46:57"
-xref: date_time_modified "2023-10-05 14:38:24"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_neutral_loss_252_mono_mass "251.105862"
-xref: spec_1_neutral_loss_252_avge_mass "251.2832"
-xref: spec_1_neutral_loss_252_flag "false"
-xref: spec_1_neutral_loss_252_composition "H(13) C(15) N(3) O"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_252_mono_mass "251.105862"
-xref: spec_2_neutral_loss_252_avge_mass "251.2832"
-xref: spec_2_neutral_loss_252_flag "false"
-xref: spec_2_neutral_loss_252_composition "H(13) C(15) N(3) O"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2079
-name: NBF
-def: "Thiol blocking reagent." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2079]
-synonym: "4-Chloro-7-nitrobenzofurazan NBD Chloride" RELATED []
-xref: record_id "2079"
-xref: delta_mono_mass "163.001791"
-xref: delta_avge_mass "163.0904"
-xref: delta_composition "H C(6) N(3) O(3)"
-xref: username_of_poster "thibautvignane"
-xref: group_of_poster ""
-xref: date_time_posted "2023-03-30 16:05:51"
-xref: date_time_modified "2024-08-12 10:35:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "R"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2080
-name: DCP
-def: "Dimedone-Based Chemical Probes." [PMID:20513473, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2080]
-synonym: "Cleaved Cysteine Sulfenic Acid Probe (DCP-Bio1) Use for enrichment of cysteine oxidation" RELATED []
-xref: record_id "2080"
-xref: delta_mono_mass "168.078644"
-xref: delta_avge_mass "168.1898"
-xref: delta_composition "H(12) C(9) O(3)"
-xref: username_of_poster "thibautvignane"
-xref: group_of_poster ""
-xref: date_time_posted "2023-04-19 18:49:30"
-xref: date_time_modified "2024-08-12 10:35:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2081
-name: Ethynyl
-def: "Ethynlation of cysteine residues." [PMID:32233093, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2081]
-xref: record_id "2081"
-xref: delta_mono_mass "24"
-xref: delta_avge_mass "24.0214"
-xref: delta_composition "C(2)"
-xref: username_of_poster "bdwyer"
-xref: group_of_poster ""
-xref: date_time_posted "2023-07-29 02:40:17"
-xref: date_time_modified "2023-10-05 14:37:06"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2082
-name: QQTGG
-def: "SUMOylation leaving QQTGG." [PMID:28112733, PMID:28112733, PMID:25218447, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2082]
-xref: record_id "2082"
-xref: delta_mono_mass "471.207761"
-xref: delta_avge_mass "471.465"
-xref: delta_composition "H(29) C(18) N(7) O(8)"
-xref: username_of_poster "jonesar"
-xref: group_of_poster ""
-xref: date_time_posted "2023-09-27 09:55:30"
-xref: date_time_modified "2023-10-05 14:36:46"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2083
-name: Pyro-QQTGG
-def: "SUMOylation leaving Pyro-QQTGG." [PMID:25218447, PMID:28112733, PMID:28112733, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2083]
-xref: record_id "2083"
-xref: delta_mono_mass "454.181212"
-xref: delta_avge_mass "454.4344"
-xref: delta_composition "H(26) C(18) N(6) O(8)"
-xref: username_of_poster "jonesar"
-xref: group_of_poster ""
-xref: date_time_posted "2023-09-27 09:57:43"
-xref: date_time_modified "2023-10-05 14:36:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2084
-name: NQTGG
-def: "SUMOylation leaving NQTGG." [PMID:32047143, PMID:29048423, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2084]
-xref: record_id "2084"
-xref: delta_mono_mass "457.192111"
-xref: delta_avge_mass "457.4384"
-xref: delta_composition "H(27) C(17) N(7) O(8)"
-xref: username_of_poster "jonesar"
-xref: group_of_poster ""
-xref: date_time_posted "2023-09-27 10:05:13"
-xref: date_time_modified "2023-10-05 14:36:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2085
-name: DVFQQQTGG
-def: "SUMOylation by Endogenous SUMO2/3 following Lys C and Asp-N serial digestion." [PMID:29942033, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2085]
-xref: record_id "2085"
-xref: delta_mono_mass "960.43011"
-xref: delta_avge_mass "960.9865"
-xref: delta_composition "H(60) C(41) N(12) O(15)"
-xref: username_of_poster "jonesar"
-xref: group_of_poster ""
-xref: date_time_posted "2023-09-27 10:06:06"
-xref: date_time_modified "2023-10-05 14:35:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2086
-name: iST-NHS specific cysteine modification
-def: "Preomics iST-NHS Kit specific cysteine modification." [URL:https\://www.preomics.com/products/ist-nhs, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2086]
-comment: The lysis buffer in the iST-NHS kit, called LYSE-NHS, does not contain primary amines and therefore does not interfere with chemical labeling. The LYSE-NHS contains a distinct alkylation agent. Please consider the following as fixed modification in your database search: Specific cysteine modification (C6H11NO), specificity [C], mass shift +113.084 Da.
-xref: record_id "2086"
-xref: delta_mono_mass "113.084064"
-xref: delta_avge_mass "113.1576"
-xref: delta_composition "H(11) C(6) N O"
-xref: username_of_poster "dzolg"
-xref: group_of_poster ""
-xref: date_time_posted "2023-12-04 11:10:14"
-xref: date_time_modified "2024-07-08 16:54:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2088
-name: Label:13C(2)15N(1)
-def: "13C(2) 15N(1) Silac label." [URL:https\://isotope.com/de-de/microbiological-and-pyrogen-tested-mpt/glycine-13c5-15n-cnlm-1673-h-mpt, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2088]
-xref: record_id "2088"
-xref: delta_mono_mass "3.003745"
-xref: delta_avge_mass "2.9787"
-xref: delta_composition "C(-2) 13C(2) N(-1) 15N"
-xref: username_of_poster "jonasfoerster"
-xref: group_of_poster ""
-xref: date_time_posted "2024-01-08 10:29:39"
-xref: date_time_modified "2024-02-29 10:49:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2106
-name: DPIA
-def: "Desthiobiotinylation of cysteine with DPIA (Desthiobiotin polyethyleneoxide iodoacetamide) probe." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2106]
-xref: record_id "2106"
-xref: delta_mono_mass "455.274384"
-xref: delta_avge_mass "455.5484"
-xref: delta_composition "H(37) C(21) N(5) O(6)"
-xref: username_of_poster "bdwyer"
-xref: group_of_poster ""
-xref: date_time_posted "2024-04-22 22:51:46"
-xref: date_time_modified "2024-04-22 22:51:46"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2107
-name: Acetoacetyl
-def: "Acetoacetylation." [URL:https\://www.genome.jp/entry/C00332, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2107]
-xref: record_id "2107"
-xref: delta_mono_mass "84.021129"
-xref: delta_avge_mass "84.0734"
-xref: delta_composition "H(4) C(4) O(2)"
-xref: username_of_poster "JakobB"
-xref: group_of_poster ""
-xref: date_time_posted "2024-06-22 12:17:22"
-xref: date_time_modified "2024-07-05 12:18:20"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2108
-name: Isovaleryl
-def: "Isovalerylation." [URL:https\://www.genome.jp/entry/C02939, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2108]
-xref: record_id "2108"
-xref: delta_mono_mass "84.057515"
-xref: delta_avge_mass "84.1164"
-xref: delta_composition "H(8) C(5) O"
-xref: username_of_poster "JakobB"
-xref: group_of_poster ""
-xref: date_time_posted "2024-06-22 12:24:23"
-xref: date_time_modified "2024-06-28 10:55:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2109
-name: 2-methylbutyryl
-def: "2-methylbutyrylation." [URL:https\://www.kegg.jp/entry/C01033, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2109]
-xref: record_id "2109"
-xref: delta_mono_mass "84.057515"
-xref: delta_avge_mass "84.1164"
-xref: delta_composition "H(8) C(5) O"
-xref: username_of_poster "JakobB"
-xref: group_of_poster ""
-xref: date_time_posted "2024-06-22 12:30:37"
-xref: date_time_modified "2024-06-28 10:57:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2110
-name: Tiglyl
-def: "Tiglylation." [URL:https\://www.genome.jp/entry/C03345, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2110]
-xref: record_id "2110"
-xref: delta_mono_mass "82.041865"
-xref: delta_avge_mass "82.1005"
-xref: delta_composition "H(6) C(5) O"
-xref: username_of_poster "JakobB"
-xref: group_of_poster ""
-xref: date_time_posted "2024-06-22 12:33:24"
-xref: date_time_modified "2024-07-05 12:15:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2111
-name: 3-methylglutaryl
-def: "3-methylglutarylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2111]
-xref: record_id "2111"
-xref: delta_mono_mass "128.047344"
-xref: delta_avge_mass "128.1259"
-xref: delta_composition "H(8) C(6) O(3)"
-xref: username_of_poster "JakobB"
-xref: group_of_poster ""
-xref: date_time_posted "2024-06-22 14:19:16"
-xref: date_time_modified "2024-06-22 14:19:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2112
-name: 3-methylglutaconyl
-def: "3-methylglutaconylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2112]
-xref: record_id "2112"
-xref: delta_mono_mass "126.031694"
-xref: delta_avge_mass "126.11"
-xref: delta_composition "H(6) C(6) O(3)"
-xref: username_of_poster "JakobB"
-xref: group_of_poster ""
-xref: date_time_posted "2024-06-22 14:21:47"
-xref: date_time_modified "2024-06-22 14:21:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2113
-name: 3-hydroxy-3-methylglutaryl
-def: "3-hydroxy-3-methylglutarylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2113]
-xref: record_id "2113"
-xref: delta_mono_mass "144.042259"
-xref: delta_avge_mass "144.1253"
-xref: delta_composition "H(8) C(6) O(4)"
-xref: username_of_poster "JakobB"
-xref: group_of_poster ""
-xref: date_time_posted "2024-06-22 14:24:06"
-xref: date_time_modified "2024-06-22 14:24:06"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2114
-name: Lactylation
-def: "Lactylation(Lac)." [PMID:31645732, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2114]
-xref: record_id "2114"
-xref: delta_mono_mass "72.021129"
-xref: delta_avge_mass "72.0627"
-xref: delta_composition "H(4) C(3) O(2)"
-xref: username_of_poster "cpu1107"
-xref: group_of_poster ""
-xref: date_time_posted "2024-06-24 10:56:15"
-xref: date_time_modified "2024-08-09 09:54:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2115
-name: Pyruvoyl
-def: "Pyruvoylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2115]
-xref: record_id "2115"
-xref: delta_mono_mass "70.005479"
-xref: delta_avge_mass "70.0468"
-xref: delta_composition "H(2) C(3) O(2)"
-xref: username_of_poster "JakobB"
-xref: group_of_poster ""
-xref: date_time_posted "2024-06-24 18:33:34"
-xref: date_time_modified "2024-08-09 09:54:42"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2116
-name: Glyoxylyl
-def: "Glyoxylylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2116]
-xref: record_id "2116"
-xref: delta_mono_mass "55.989829"
-xref: delta_avge_mass "56.0202"
-xref: delta_composition "C(2) O(2)"
-xref: username_of_poster "JakobB"
-xref: group_of_poster ""
-xref: date_time_posted "2024-06-24 19:20:20"
-xref: date_time_modified "2024-08-09 09:54:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2117
-name: Itaconatyl
-def: "Itaconatylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2117]
-xref: record_id "2117"
-xref: delta_mono_mass "130.026609"
-xref: delta_avge_mass "130.0987"
-xref: delta_composition "H(6) C(5) O(4)"
-xref: username_of_poster "JakobB"
-xref: group_of_poster ""
-xref: date_time_posted "2024-06-24 20:02:30"
-xref: date_time_modified "2024-08-09 09:55:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2118
-name: Itaconyl
-def: "Itaconylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2118]
-xref: record_id "2118"
-xref: delta_mono_mass "112.016044"
-xref: delta_avge_mass "112.0835"
-xref: delta_composition "H(4) C(5) O(3)"
-xref: username_of_poster "JakobB"
-xref: group_of_poster ""
-xref: date_time_posted "2024-06-26 14:01:07"
-xref: date_time_modified "2024-08-09 09:55:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2119
-name: ValGly
-def: "UFMylation residue." [PMID:8383789, PMID:33066455, PMID:http://www.ncbi.nlm.nih.gov/pubmed/35756382, PMID:35756382, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2119]
-comment: The valine glycine residues left on ufmylated lysine after tryptic digestion.
-synonym: "UFMylation leaving VG tag valineglycine" RELATED []
-xref: record_id "2119"
-xref: delta_mono_mass "156.089878"
-xref: delta_avge_mass "156.1824"
-xref: delta_composition "H(12) C(7) N(2) O(2)"
-xref: username_of_poster "pscaturro"
-xref: group_of_poster ""
-xref: date_time_posted "2024-06-26 14:09:36"
-xref: date_time_modified "2024-06-26 14:09:36"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2120
-name: Pentanoyl
-def: "Pentanoylation." [URL:https\://www.genome.jp/entry/C00888, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2120]
-synonym: "Valeryl" RELATED []
-xref: record_id "2120"
-xref: delta_mono_mass "84.057515"
-xref: delta_avge_mass "84.1164"
-xref: delta_composition "H(8) C(5) O"
-xref: username_of_poster "JakobB"
-xref: group_of_poster ""
-xref: date_time_posted "2024-06-26 14:12:23"
-xref: date_time_modified "2024-06-28 10:53:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2121
-name: Hexanoyl
-def: "Hexanoylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2121]
-xref: record_id "2121"
-xref: delta_mono_mass "98.073165"
-xref: delta_avge_mass "98.143"
-xref: delta_composition "H(10) C(6) O"
-xref: username_of_poster "JakobB"
-xref: group_of_poster ""
-xref: date_time_posted "2024-06-26 14:24:17"
-xref: date_time_modified "2024-06-26 14:24:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2122
-name: Label:13C(6)15N(2)+TMT6plex
-def: "Sixplex Tandem Mass Tag 13C(6) 15N(2) Silac label." [PMID:34847359, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2122]
-comment: Tandem Mass Tag and TMT are registered Trademarks of Proteome Sciences plc.
-xref: record_id "2122"
-xref: delta_mono_mass "237.177131"
-xref: delta_avge_mass "237.2062"
-xref: delta_composition "H(20) C(2) 13C(10) N(-1) 15N(3) O(2)"
-xref: username_of_poster "dzolg"
-xref: group_of_poster ""
-xref: date_time_posted "2024-07-01 12:49:15"
-xref: date_time_modified "2024-08-12 11:33:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Multiple"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2123
-name: Label:13C(6)15N(2)+TMTpro
-def: "TMTpro Tandem Mass Tag 13C(6) 15N(2) Silac label." [PMID:34847359, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2123]
-comment: Tandem Mass Tag and TMT are registered Trademarks of Proteome Sciences plc.
-xref: record_id "2123"
-xref: delta_mono_mass "312.221344"
-xref: delta_avge_mass "312.2554"
-xref: delta_composition "H(25) C(2) 13C(13) N(-1) 15N(4) O(3)"
-xref: username_of_poster "dzolg"
-xref: group_of_poster ""
-xref: date_time_posted "2024-07-01 12:51:56"
-xref: date_time_modified "2024-08-12 11:33:20"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Multiple"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2126
-name: 2PCA-triazole-ethanethiol
-def: "Cleaved 2PCA clicked to biotin-SS-azide." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2126]
-xref: record_id "2126"
-xref: delta_mono_mass "216.046967"
-xref: delta_avge_mass "216.2623"
-xref: delta_composition "H(8) C(10) N(4) S"
-xref: username_of_poster "pscaturro"
-xref: group_of_poster ""
-xref: date_time_posted "2024-07-08 10:09:29"
-xref: date_time_modified "2024-08-09 09:56:09"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
diff --git a/rustyms-generate-databases/data/unimod_in_place.obo b/rustyms-generate-databases/data/unimod_in_place.obo
deleted file mode 100644
index 7c282fe2..00000000
--- a/rustyms-generate-databases/data/unimod_in_place.obo
+++ /dev/null
@@ -1,46331 +0,0 @@
-format-version: 1.4
-date: 12:08:2024 11:33
-
-saved-by: psi-pi_team
-default-namespace: UNIMOD
-
-[Term]
-id: UNIMOD:0
-name: unimod root node
-def: "The root node of the unimod modifications ontology." [UNIMOD:0]
-
-[Term]
-id: UNIMOD:1
-name: Acetyl
-def: "Acetylation." [RESID:AA0048, RESID:AA0049, RESID:AA0041, RESID:AA0052, RESID:AA0364, RESID:AA0056, RESID:AA0046, RESID:AA0051, RESID:AA0045, RESID:AA0354, RESID:AA0044, RESID:AA0043, PMID:11999733, URL:http\://www.ionsource.com/Card/acetylation/acetylation.htm, RESID:AA0055, PMID:14730666, PMID:15350136, RESID:AA0047, PMID:12175151, PMID:11857757, RESID:AA0042, RESID:AA0050, RESID:AA0053, RESID:AA0054, FindMod:ACET, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1]
-xref: record_id "1"
-xref: delta_mono_mass "42.010565"
-xref: delta_avge_mass "42.0367"
-xref: delta_composition "H(2) C(2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2017-11-08 16:08:56"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Multiple"
-xref: spec_1_misc_notes "PT and GIST acetyl light"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Multiple"
-xref: spec_2_misc_notes "GIST acetyl light"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "C"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "S"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Post-translational"
-xref: spec_5_group "5"
-xref: spec_5_hidden "0"
-xref: spec_5_site "N-term"
-xref: spec_5_position "Protein N-term"
-xref: spec_5_classification "Post-translational"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "T"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Post-translational"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "Y"
-xref: spec_7_position "Anywhere"
-xref: spec_7_classification "Chemical derivative"
-xref: spec_7_misc_notes "O-acetyl"
-xref: spec_8_group "8"
-xref: spec_8_hidden "1"
-xref: spec_8_site "H"
-xref: spec_8_position "Anywhere"
-xref: spec_8_classification "Chemical derivative"
-xref: spec_9_group "9"
-xref: spec_9_hidden "1"
-xref: spec_9_site "R"
-xref: spec_9_position "Anywhere"
-xref: spec_9_classification "Artefact"
-xref: spec_9_misc_notes "glyoxal-derived hydroimidazolone"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2
-name: Amidated
-def: "Amidation." [RESID:AA0088, RESID:AA0087, RESID:AA0086, RESID:AA0085, RESID:AA0084, RESID:AA0083, RESID:AA0082, RESID:AA0081, RESID:AA0089, RESID:AA0090, RESID:AA0091, RESID:AA0092, RESID:AA0093, RESID:AA0094, RESID:AA0095, RESID:AA0096, RESID:AA0097, RESID:AA0098, RESID:AA0099, RESID:AA0100, FindMod:AMID, PMID:14588022, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2]
-synonym: "Top-Down sequencing c-type fragment ion" RELATED []
-xref: record_id "2"
-xref: delta_mono_mass "-0.984016"
-xref: delta_avge_mass "-0.9848"
-xref: delta_composition "H N O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2010-06-28 10:52:25"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Protein C-term"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-xref: spec_2_misc_notes "MS/MS experiments of mass spectrometric c-ions (MS^3) can be used for protein identification by library searching. T3-sequencing is such a technique (see reference). Search engines must recognize this as a virtual modification."
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:3
-name: Biotin
-def: "Biotinylation." [RESID:AA0117, FindMod:BIOT, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=3]
-xref: record_id "3"
-xref: delta_mono_mass "226.077598"
-xref: delta_avge_mass "226.2954"
-xref: delta_composition "H(14) C(10) N(2) O(2) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2017-10-09 15:45:09"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:4
-name: Carbamidomethyl
-def: "Iodoacetamide derivative." [PMID:11510821, PMID:12422359, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=4]
-synonym: "Carboxyamidomethylation" RELATED []
-xref: record_id "4"
-xref: delta_mono_mass "57.021464"
-xref: delta_avge_mass "57.0513"
-xref: delta_composition "H(3) C(2) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2017-10-09 10:27:10"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "0"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Artefact"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "H"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Artefact"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "D"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Artefact"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "E"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Artefact"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "S"
-xref: spec_7_position "Anywhere"
-xref: spec_7_classification "Artefact"
-xref: spec_8_group "8"
-xref: spec_8_hidden "1"
-xref: spec_8_site "T"
-xref: spec_8_position "Anywhere"
-xref: spec_8_classification "Artefact"
-xref: spec_9_group "9"
-xref: spec_9_hidden "1"
-xref: spec_9_site "Y"
-xref: spec_9_position "Anywhere"
-xref: spec_9_classification "Artefact"
-xref: spec_10_group "10"
-xref: spec_10_hidden "1"
-xref: spec_10_site "U"
-xref: spec_10_position "Anywhere"
-xref: spec_10_classification "Chemical derivative"
-xref: spec_11_group "11"
-xref: spec_11_hidden "1"
-xref: spec_11_site "M"
-xref: spec_11_position "Anywhere"
-xref: spec_11_classification "Chemical derivative"
-xref: spec_11_neutral_loss_0_mono_mass "0"
-xref: spec_11_neutral_loss_0_avge_mass "0"
-xref: spec_11_neutral_loss_0_flag "false"
-xref: spec_11_neutral_loss_0_composition "0"
-xref: spec_11_neutral_loss_106_mono_mass "105.024835"
-xref: spec_11_neutral_loss_106_avge_mass "105.1588"
-xref: spec_11_neutral_loss_106_flag "false"
-xref: spec_11_neutral_loss_106_composition "H(7) C(3) N O S"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:5
-name: Carbamyl
-def: "Carbamylation." [PMID:12203680, RESID:AA0343, PMID:10978403, RESID:AA0332, URL:http\://www.ionsource.com/Card/carbam/carbam.htm, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=5]
-comment: Carbamylation is an irreversible process of non-enzymatic modification of proteins by the breakdown products of urea isocyanic acid reacts with the N-term of a proteine or side chains of lysine and arginine residues.
-xref: record_id "5"
-xref: delta_mono_mass "43.005814"
-xref: delta_avge_mass "43.0247"
-xref: delta_composition "H C N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2011-11-21 13:06:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Multiple"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Multiple"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "R"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Artefact"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "C"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Artefact"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "M"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Artefact"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "S"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "T"
-xref: spec_7_position "Anywhere"
-xref: spec_7_classification "Chemical derivative"
-xref: spec_8_group "8"
-xref: spec_8_hidden "1"
-xref: spec_8_site "Y"
-xref: spec_8_position "Anywhere"
-xref: spec_8_classification "Chemical derivative"
-xref: spec_9_group "9"
-xref: spec_9_hidden "1"
-xref: spec_9_site "N-term"
-xref: spec_9_position "Protein N-term"
-xref: spec_9_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:6
-name: Carboxymethyl
-def: "Iodoacetic acid derivative." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=6]
-synonym: "Carboxymethylation" RELATED []
-xref: record_id "6"
-xref: delta_mono_mass "58.005479"
-xref: delta_avge_mass "58.0361"
-xref: delta_composition "H(2) C(2) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2016-02-01 14:17:55"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Artefact"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "W"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_4_misc_notes "Hydroxylethanone"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "U"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:7
-name: Deamidated
-def: "Deamidation." [PMID:6838602, RESID:AA0214, URL:http\://www.ionsource.com/Card/Deamidation/deamidation.htm, FindMod:CITR, RESID:AA0128, FindMod:FLAC, PMID:15700232, FindMod:DEAM, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=7]
-synonym: "phenyllactyl from N-term Phe Citrullination" RELATED []
-xref: record_id "7"
-xref: delta_mono_mass "0.984016"
-xref: delta_avge_mass "0.9848"
-xref: delta_composition "H(-1) N(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2018-10-25 09:32:26"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_misc_notes "Convertion of glycosylated asparagine residues upon deglycosylation with PNGase F in H2O"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "R"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_2_misc_notes "Protein which is post-translationally modified by the de-imination of one or more arginine residues; Peptidylarginine deiminase (PAD) converts protein bound to citrulline"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_44_mono_mass "43.005814"
-xref: spec_2_neutral_loss_44_avge_mass "43.0247"
-xref: spec_2_neutral_loss_44_flag "false"
-xref: spec_2_neutral_loss_44_composition "H C N O"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "F"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:8
-name: ICAT-G
-def: "Gygi ICAT(TM) d0." [PMID:10504701, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=8]
-xref: record_id "8"
-xref: delta_mono_mass "486.251206"
-xref: delta_avge_mass "486.6253"
-xref: delta_composition "H(38) C(22) N(4) O(6) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-16 17:00:43"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:9
-name: ICAT-G:2H(8)
-def: "Gygi ICAT(TM) d8." [PMID:10504701, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=9]
-xref: record_id "9"
-xref: delta_mono_mass "494.30142"
-xref: delta_avge_mass "494.6746"
-xref: delta_composition "H(30) 2H(8) C(22) N(4) O(6) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-16 17:01:35"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:10
-name: Met->Hse
-def: "Homoserine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=10]
-comment: Cyanogen bromide (CNBr) cleavage converts the C-term Met to either homoserine or homoserine lactone, depending on pH.
-xref: record_id "10"
-xref: delta_mono_mass "-29.992806"
-xref: delta_avge_mass "-30.0922"
-xref: delta_composition "H(-2) C(-1) O S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-13 15:40:08"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "M"
-xref: spec_1_position "Any C-term"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:11
-name: Met->Hsl
-def: "Homoserine lactone." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=11]
-comment: Cyanogen bromide (CNBr) cleavage converts the C-term Met to either homoserine or homoserine lactone, depending on pH.
-xref: record_id "11"
-xref: delta_mono_mass "-48.003371"
-xref: delta_avge_mass "-48.1075"
-xref: delta_composition "H(-4) C(-1) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-11-14 11:10:15"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "M"
-xref: spec_1_position "Any C-term"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:12
-name: ICAT-D:2H(8)
-def: "Applied Biosystems original ICAT(TM) d8." [URL:http\://www.chemsoc.org/exemplarchem/entries/2002/proteomics/images/icat_reagent.gif, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=12]
-xref: record_id "12"
-xref: delta_mono_mass "450.275205"
-xref: delta_avge_mass "450.6221"
-xref: delta_composition "H(26) 2H(8) C(20) N(4) O(5) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-16 16:56:23"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:13
-name: ICAT-D
-def: "Applied Biosystems original ICAT(TM) d0." [URL:http\://www.chemsoc.org/exemplarchem/entries/2002/proteomics/images/icat_reagent.gif, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=13]
-xref: record_id "13"
-xref: delta_mono_mass "442.224991"
-xref: delta_avge_mass "442.5728"
-xref: delta_composition "H(34) C(20) N(4) O(5) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-16 16:53:48"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:17
-name: NIPCAM
-def: "N-isopropylcarboxamidomethyl." [PMID:8465942, PMID:11465505, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=17]
-synonym: "Dimethylacrylamide, DMA" RELATED []
-xref: record_id "17"
-xref: delta_mono_mass "99.068414"
-xref: delta_avge_mass "99.1311"
-xref: delta_composition "H(9) C(5) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-16 12:39:14"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:20
-name: PEO-Iodoacetyl-LC-Biotin
-def: "Biotinyl-iodoacetamidyl-3,6-dioxaoctanediamine." [PMID:12038753, PMID:15253424, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=20]
-synonym: "Pierce EZ-Link PEO-Iodoacetyl Biotin" RELATED []
-xref: record_id "20"
-xref: delta_mono_mass "414.193691"
-xref: delta_avge_mass "414.5196"
-xref: delta_composition "H(30) C(18) N(4) O(5) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-11-14 11:40:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:21
-name: Phospho
-def: "Phosphorylation." [RESID:AA0036, URL:http\://www.ionsource.com/Card/phos/phos.htm, RESID:AA0037, RESID:AA0033, RESID:AA0038, RESID:AA0039, RESID:AA0222, FindMod:PHOS, RESID:AA0034, RESID:AA0035, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=21]
-comment: Neutral loss of phosphate is typically observed from Y/H/D/E/K/C, rather than the preferential loss of phosphoric acid from S/T.
-xref: record_id "21"
-xref: delta_mono_mass "79.966331"
-xref: delta_avge_mass "79.9799"
-xref: delta_composition "H O(3) P"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2018-08-13 13:42:59"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_1_neutral_loss_98_mono_mass "97.976896"
-xref: spec_1_neutral_loss_98_avge_mass "97.9952"
-xref: spec_1_neutral_loss_98_flag "false"
-xref: spec_1_neutral_loss_98_composition "H(3) O(4) P"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_98_mono_mass "97.976896"
-xref: spec_1_neutral_loss_98_avge_mass "97.9952"
-xref: spec_1_neutral_loss_98_flag "false"
-xref: spec_1_neutral_loss_98_composition "H(3) O(4) P"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "Y"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "D"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-xref: spec_3_misc_notes "Rare"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "H"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Post-translational"
-xref: spec_4_misc_notes "Rare"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "C"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Post-translational"
-xref: spec_5_misc_notes "Rare"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "R"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Post-translational"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "K"
-xref: spec_7_position "Anywhere"
-xref: spec_7_classification "Post-translational"
-xref: spec_8_group "8"
-xref: spec_8_hidden "1"
-xref: spec_8_site "E"
-xref: spec_8_position "Anywhere"
-xref: spec_8_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:23
-name: Dehydrated
-def: "Dehydration." [FindMod:DHAS, RESID:AA0303, RESID:AA0302, RESID:AA0181, RESID:AA0182, FindMod:DHB, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=23]
-synonym: "didehydroalanine C-terminal imide Prompt loss of phosphate from phosphorylated residue D-Succinimide" RELATED []
-xref: record_id "23"
-xref: delta_mono_mass "-18.010565"
-xref: delta_avge_mass "-18.0153"
-xref: delta_composition "H(-2) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-11-14 11:05:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Protein C-term"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "Q"
-xref: spec_2_position "Protein C-term"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "S"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-xref: spec_3_misc_notes "beta-elimination"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "T"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Post-translational"
-xref: spec_4_misc_notes "beta-elimination"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "Y"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Post-translational"
-xref: spec_5_misc_notes "beta-elimination"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "D"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-xref: spec_7_group "7"
-xref: spec_7_hidden "0"
-xref: spec_7_site "C"
-xref: spec_7_position "Any N-term"
-xref: spec_7_classification "Artefact"
-xref: spec_7_misc_notes "Pyro-carboxymethyl as a delta from Carboxymethyl-Cys"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:24
-name: Propionamide
-def: "Acrylamide adduct." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=24]
-xref: record_id "24"
-xref: delta_mono_mass "71.037114"
-xref: delta_avge_mass "71.0779"
-xref: delta_composition "H(5) C(3) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2024-08-12 09:49:28"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:25
-name: Pyridylacetyl
-def: "Pyridylacetyl." [PMID:9276974, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=25]
-xref: record_id "25"
-xref: delta_mono_mass "119.037114"
-xref: delta_avge_mass "119.1207"
-xref: delta_composition "H(5) C(7) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-16 12:47:43"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:26
-name: Pyro-carbamidomethyl
-def: "S-carbamoylmethylcysteine cyclization (N-terminus)." [PMID:12643538, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=26]
-comment: Cyclisation of N-term Carbamidomethyl-Cys or Carboxymethyl-Cys. The delta is relative to Cys. For a delta relative to alkylated Cys, see Ammonia-loss and Dehydrated.
-synonym: "Carboxymethyl-Cys cyclization (N-terminus) Carbamidomethyl-Cys cyclization (N-terminus)" RELATED []
-xref: record_id "26"
-xref: delta_mono_mass "39.994915"
-xref: delta_avge_mass "40.0208"
-xref: delta_composition "C(2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-11-14 11:05:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "C"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:27
-name: Glu->pyro-Glu
-def: "Pyro-glu from E." [RESID:AA0031, PMID:8442665, FindMod:PYRE, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=27]
-xref: record_id "27"
-xref: delta_mono_mass "-18.010565"
-xref: delta_avge_mass "-18.0153"
-xref: delta_composition "H(-2) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2008-06-05 13:54:56"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "E"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:28
-name: Gln->pyro-Glu
-def: "Pyro-glu from Q." [RESID:AA0031, FindMod:PYRR, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=28]
-xref: record_id "28"
-xref: delta_mono_mass "-17.026549"
-xref: delta_avge_mass "-17.0305"
-xref: delta_composition "H(-3) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-13 17:06:57"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "Q"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:29
-name: SMA
-def: "N-Succinimidyl-2-morpholine acetate." [PMID:10446193, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=29]
-xref: record_id "29"
-xref: delta_mono_mass "127.063329"
-xref: delta_avge_mass "127.1412"
-xref: delta_composition "H(9) C(6) N O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2010-11-03 17:44:14"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:30
-name: Cation:Na
-def: "Sodium adduct." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=30]
-comment: Proton replaced by sodium cation.
-xref: record_id "30"
-xref: delta_mono_mass "21.981943"
-xref: delta_avge_mass "21.9818"
-xref: delta_composition "H(-1) Na"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-14 19:43:17"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Any C-term"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "D"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "E"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:31
-name: Pyridylethyl
-def: "S-pyridylethylation." [PMID:11760118, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=31]
-xref: record_id "31"
-xref: delta_mono_mass "105.057849"
-xref: delta_avge_mass "105.1372"
-xref: delta_composition "H(7) C(7) N"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-16 12:43:38"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:34
-name: Methyl
-def: "Methylation." [RESID:AA0105, PMID:11875433, RESID:AA0072, RESID:AA0299, RESID:AA0337, RESID:AA0317, RESID:AA0273, RESID:AA0234, RESID:AA0073, RESID:AA0070, RESID:AA0071, RESID:AA0076, RESID:AA0272, RESID:AA0305, RESID:AA0336, RESID:AA0069, RESID:AA0065, RESID:AA0063, RESID:AA0061, RESID:AA0064, RESID:AA0338, RESID:AA0318, FindMod:METH, URL:http\://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2921173&tool=pmcentrez&rendertype=abstract, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=34]
-synonym: "methyl ester" RELATED []
-xref: record_id "34"
-xref: delta_mono_mass "14.01565"
-xref: delta_avge_mass "14.0266"
-xref: delta_composition "H(2) C"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2015-08-26 14:39:25"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "N"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Post-translational"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "N-term"
-xref: spec_5_position "Any N-term"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "Q"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Post-translational"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "R"
-xref: spec_7_position "Anywhere"
-xref: spec_7_classification "Post-translational"
-xref: spec_8_group "8"
-xref: spec_8_hidden "1"
-xref: spec_8_site "I"
-xref: spec_8_position "Anywhere"
-xref: spec_8_classification "Post-translational"
-xref: spec_9_group "9"
-xref: spec_9_hidden "1"
-xref: spec_9_site "L"
-xref: spec_9_position "Anywhere"
-xref: spec_9_classification "Post-translational"
-xref: spec_10_group "10"
-xref: spec_10_hidden "1"
-xref: spec_10_site "N-term"
-xref: spec_10_position "Protein N-term"
-xref: spec_10_classification "Post-translational"
-xref: spec_11_group "11"
-xref: spec_11_hidden "0"
-xref: spec_11_site "C-term"
-xref: spec_11_position "Any C-term"
-xref: spec_11_classification "Multiple"
-xref: spec_12_group "12"
-xref: spec_12_hidden "0"
-xref: spec_12_site "E"
-xref: spec_12_position "Anywhere"
-xref: spec_12_classification "Post-translational"
-xref: spec_12_group "12"
-xref: spec_12_hidden "0"
-xref: spec_12_site "D"
-xref: spec_12_position "Anywhere"
-xref: spec_12_classification "Post-translational"
-xref: spec_13_group "13"
-xref: spec_13_hidden "1"
-xref: spec_13_site "S"
-xref: spec_13_position "Anywhere"
-xref: spec_13_classification "Post-translational"
-xref: spec_14_group "14"
-xref: spec_14_hidden "1"
-xref: spec_14_site "T"
-xref: spec_14_position "Anywhere"
-xref: spec_14_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:35
-name: Oxidation
-def: "Oxidation or Hydroxylation." [RESID:AA0027, PMID:11461766, RESID:AA0029, RESID:AA0028, RESID:AA0030, PMID:9004526, RESID:AA0205, RESID:AA0146, FindMod:DOPA, RESID:AA0215, FindMod:CSEA, RESID:AA0026, PMID:14661084, PMID:15569593, PMID:11120890, PMID:11212008, RESID:AA0322, RESID:AA0235, FindMod:HYDR, PMID:14661085, PMID:12781462, PMID:2057999, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=35]
-xref: record_id "35"
-xref: delta_mono_mass "15.994915"
-xref: delta_avge_mass "15.9994"
-xref: delta_composition "O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2017-10-06 17:05:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_1_misc_notes "3-hydroxyaspartic acid"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-xref: spec_3_misc_notes "3-hydroxyasparagine"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "P"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Post-translational"
-xref: spec_4_misc_notes "glutamic semialdehyde"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "F"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Artefact"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "Y"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Post-translational"
-xref: spec_6_misc_notes "dihydroxyphenylalanine (DOPA)"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "R"
-xref: spec_7_position "Anywhere"
-xref: spec_7_classification "Post-translational"
-xref: spec_8_group "8"
-xref: spec_8_hidden "0"
-xref: spec_8_site "M"
-xref: spec_8_position "Anywhere"
-xref: spec_8_classification "Artefact"
-xref: spec_8_misc_notes "methionine sulfoxide"
-xref: spec_8_neutral_loss_0_mono_mass "0"
-xref: spec_8_neutral_loss_0_avge_mass "0"
-xref: spec_8_neutral_loss_0_flag "false"
-xref: spec_8_neutral_loss_0_composition "0"
-xref: spec_8_neutral_loss_64_mono_mass "63.998285"
-xref: spec_8_neutral_loss_64_avge_mass "64.1069"
-xref: spec_8_neutral_loss_64_flag "false"
-xref: spec_8_neutral_loss_64_composition "H(4) C O S"
-xref: spec_9_group "9"
-xref: spec_9_hidden "1"
-xref: spec_9_site "C"
-xref: spec_9_position "Anywhere"
-xref: spec_9_classification "Post-translational"
-xref: spec_9_misc_notes "sulfenic acid"
-xref: spec_10_group "10"
-xref: spec_10_hidden "0"
-xref: spec_10_site "W"
-xref: spec_10_position "Anywhere"
-xref: spec_10_classification "Artefact"
-xref: spec_10_group "10"
-xref: spec_10_hidden "0"
-xref: spec_10_site "H"
-xref: spec_10_position "Anywhere"
-xref: spec_10_classification "Artefact"
-xref: spec_10_misc_notes "2-oxohistidine"
-xref: spec_11_group "11"
-xref: spec_11_hidden "1"
-xref: spec_11_site "G"
-xref: spec_11_position "Any C-term"
-xref: spec_11_classification "Pre-translational"
-xref: spec_11_misc_notes "Hydroxyglycine derivative in amidation pathway"
-xref: spec_12_group "12"
-xref: spec_12_hidden "1"
-xref: spec_12_site "U"
-xref: spec_12_position "Anywhere"
-xref: spec_12_classification "Multiple"
-xref: spec_13_group "13"
-xref: spec_13_hidden "1"
-xref: spec_13_site "E"
-xref: spec_13_position "Anywhere"
-xref: spec_13_classification "Chemical derivative"
-xref: spec_13_misc_notes "hydroxyglutamic acid"
-xref: spec_14_group "14"
-xref: spec_14_hidden "1"
-xref: spec_14_site "I"
-xref: spec_14_position "Anywhere"
-xref: spec_14_classification "Chemical derivative"
-xref: spec_15_group "15"
-xref: spec_15_hidden "1"
-xref: spec_15_site "L"
-xref: spec_15_position "Anywhere"
-xref: spec_15_classification "Chemical derivative"
-xref: spec_16_group "16"
-xref: spec_16_hidden "1"
-xref: spec_16_site "Q"
-xref: spec_16_position "Anywhere"
-xref: spec_16_classification "Chemical derivative"
-xref: spec_17_group "17"
-xref: spec_17_hidden "1"
-xref: spec_17_site "S"
-xref: spec_17_position "Anywhere"
-xref: spec_17_classification "Chemical derivative"
-xref: spec_18_group "18"
-xref: spec_18_hidden "1"
-xref: spec_18_site "T"
-xref: spec_18_position "Anywhere"
-xref: spec_18_classification "Chemical derivative"
-xref: spec_19_group "19"
-xref: spec_19_hidden "1"
-xref: spec_19_site "V"
-xref: spec_19_position "Anywhere"
-xref: spec_19_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:36
-name: Dimethyl
-def: "Di-Methylation." [FindMod:DIMETH, RESID:AA0311, RESID:AA0068, PMID:14570711, RESID:AA0067, PMID:12964758, RESID:AA0075, RESID:AA0066, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=36]
-xref: record_id "36"
-xref: delta_mono_mass "28.0313"
-xref: delta_avge_mass "28.0532"
-xref: delta_composition "H(4) C(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2014-11-16 07:37:54"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Multiple"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "R"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Isotopic label"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "N"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Post-translational"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "P"
-xref: spec_5_position "Protein N-term"
-xref: spec_5_classification "Post-translational"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "N-term"
-xref: spec_6_position "Protein N-term"
-xref: spec_6_classification "Isotopic label"
-xref: spec_6_misc_notes "When dimethyl labelling is pre-digest"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:37
-name: Trimethyl
-def: "Tri-Methylation." [FindMod:TRIMETH, RESID:AA0062, RESID:AA0074, PMID:12590383, URL:http\://pir.georgetown.edu/resid/faq.shtml#q12, URL:http\://www.cancerci.com/content/1/1/3, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=37]
-xref: record_id "37"
-xref: delta_mono_mass "42.04695"
-xref: delta_avge_mass "42.0797"
-xref: delta_composition "H(6) C(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2015-05-22 13:05:59"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_60_mono_mass "59.073499"
-xref: spec_1_neutral_loss_60_avge_mass "59.1103"
-xref: spec_1_neutral_loss_60_flag "false"
-xref: spec_1_neutral_loss_60_composition "H(9) C(3) N"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "R"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "A"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:39
-name: Methylthio
-def: "Beta-methylthiolation." [RESID:AA0320, PMID:8844851, URL:http\://www.trc-canada.com/white_papers.lasso, RESID:AA0232, URL:http\://docs.appliedbiosystems.com/pebiodocs/04351918.pdf, RESID:AA0101, FindMod:BMTH, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=39]
-synonym: "Methyl methanethiosulfonate MMTS" RELATED []
-xref: record_id "39"
-xref: delta_mono_mass "45.987721"
-xref: delta_avge_mass "46.0916"
-xref: delta_composition "H(2) C S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2011-11-24 16:48:21"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "0"
-xref: spec_3_site "C"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Multiple"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "N-term"
-xref: spec_4_position "Any N-term"
-xref: spec_4_classification "Artefact"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "K"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:40
-name: Sulfo
-def: "O-Sulfonation." [RESID:AA0172, PMID:14752058, RESID:AA0362, FindMod:SULF, RESID:AA0171, RESID:AA0361, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=40]
-xref: record_id "40"
-xref: delta_mono_mass "79.956815"
-xref: delta_avge_mass "80.0632"
-xref: delta_composition "O(3) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2012-02-14 17:50:32"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_1_misc_notes "Because the modification is quantitatively lost on CID, site assigment is not possible when there is a choice of sites"
-xref: spec_1_neutral_loss_80_mono_mass "79.956815"
-xref: spec_1_neutral_loss_80_avge_mass "80.0632"
-xref: spec_1_neutral_loss_80_flag "false"
-xref: spec_1_neutral_loss_80_composition "O(3) S"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_1_misc_notes "Because the modification is quantitatively lost on CID, site assigment is not possible when there is a choice of sites"
-xref: spec_1_neutral_loss_80_mono_mass "79.956815"
-xref: spec_1_neutral_loss_80_avge_mass "80.0632"
-xref: spec_1_neutral_loss_80_flag "false"
-xref: spec_1_neutral_loss_80_composition "O(3) S"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_1_misc_notes "Because the modification is quantitatively lost on CID, site assigment is not possible when there is a choice of sites"
-xref: spec_1_neutral_loss_80_mono_mass "79.956815"
-xref: spec_1_neutral_loss_80_avge_mass "80.0632"
-xref: spec_1_neutral_loss_80_flag "false"
-xref: spec_1_neutral_loss_80_composition "O(3) S"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_2_misc_notes "Sulfitolysis"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:41
-name: Hex
-def: "Hexose." [RESID:AA0217, RESID:AA0152, PMID:15279557, FindMod:GLUC, URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&mode=exact, RESID:AA0157, FindMod:CMAN, RESID:AA0327, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=41]
-synonym: "Fructose Mannose Galactose Glucose" RELATED []
-xref: record_id "41"
-xref: delta_mono_mass "162.052824"
-xref: delta_avge_mass "162.1406"
-xref: delta_composition "Hex"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2018-06-27 13:23:10"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other glycosylation"
-xref: spec_1_misc_notes "glycation"
-xref: spec_1_neutral_loss_55_mono_mass "54.031694"
-xref: spec_1_neutral_loss_55_avge_mass "54.0458"
-xref: spec_1_neutral_loss_55_flag "false"
-xref: spec_1_neutral_loss_55_composition "H(6) O(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other glycosylation"
-xref: spec_1_misc_notes "glycation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_55_mono_mass "54.031694"
-xref: spec_1_neutral_loss_55_avge_mass "54.0458"
-xref: spec_1_neutral_loss_55_flag "false"
-xref: spec_1_neutral_loss_55_composition "H(6) O(3)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_163_mono_mass "162.052824"
-xref: spec_2_neutral_loss_163_avge_mass "162.1406"
-xref: spec_2_neutral_loss_163_flag "false"
-xref: spec_2_neutral_loss_163_composition "Hex"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Other glycosylation"
-xref: spec_3_misc_notes "glycation"
-xref: spec_3_neutral_loss_0_mono_mass "0"
-xref: spec_3_neutral_loss_0_avge_mass "0"
-xref: spec_3_neutral_loss_0_flag "false"
-xref: spec_3_neutral_loss_0_composition "0"
-xref: spec_3_neutral_loss_55_mono_mass "54.031694"
-xref: spec_3_neutral_loss_55_avge_mass "54.0458"
-xref: spec_3_neutral_loss_55_flag "false"
-xref: spec_3_neutral_loss_55_composition "H(6) O(3)"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "T"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "O-linked glycosylation"
-xref: spec_4_neutral_loss_163_mono_mass "162.052824"
-xref: spec_4_neutral_loss_163_avge_mass "162.1406"
-xref: spec_4_neutral_loss_163_flag "false"
-xref: spec_4_neutral_loss_163_composition "Hex"
-xref: spec_4_neutral_loss_0_mono_mass "0"
-xref: spec_4_neutral_loss_0_avge_mass "0"
-xref: spec_4_neutral_loss_0_flag "false"
-xref: spec_4_neutral_loss_0_composition "0"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "S"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "O-linked glycosylation"
-xref: spec_4_neutral_loss_163_mono_mass "162.052824"
-xref: spec_4_neutral_loss_163_avge_mass "162.1406"
-xref: spec_4_neutral_loss_163_flag "false"
-xref: spec_4_neutral_loss_163_composition "Hex"
-xref: spec_4_neutral_loss_0_mono_mass "0"
-xref: spec_4_neutral_loss_0_avge_mass "0"
-xref: spec_4_neutral_loss_0_flag "false"
-xref: spec_4_neutral_loss_0_composition "0"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "W"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Other glycosylation"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "C"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Other glycosylation"
-xref: spec_8_group "8"
-xref: spec_8_hidden "1"
-xref: spec_8_site "Y"
-xref: spec_8_position "Anywhere"
-xref: spec_8_classification "O-linked glycosylation"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:42
-name: Lipoyl
-def: "Lipoyl." [RESID:AA0118, FindMod:LIPY, PMID:3522581, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=42]
-comment: This group is normally a substituent on N6 of a lysine residue of an enzyme or other protein.
-xref: record_id "42"
-xref: delta_mono_mass "188.032956"
-xref: delta_avge_mass "188.3103"
-xref: delta_composition "H(12) C(8) O S(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-16 15:06:53"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:43
-name: HexNAc
-def: "N-Acetylhexosamine." [FindMod:GLCN, RESID:AA0155, PMID:3086323, RESID:AA0154, RESID:AA0151, URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=43]
-comment: The amine derivative of a hexose formed by replacing a hydroxyl group with an amino group.(+acetyl group).
-xref: record_id "43"
-xref: delta_mono_mass "203.079373"
-xref: delta_avge_mass "203.1925"
-xref: delta_composition "HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2024-08-12 09:50:41"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_204_mono_mass "203.079373"
-xref: spec_1_neutral_loss_204_avge_mass "203.1925"
-xref: spec_1_neutral_loss_204_flag "false"
-xref: spec_1_neutral_loss_204_composition "HexNAc"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_204_mono_mass "203.079373"
-xref: spec_2_neutral_loss_204_avge_mass "203.1925"
-xref: spec_2_neutral_loss_204_flag "false"
-xref: spec_2_neutral_loss_204_composition "HexNAc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_204_mono_mass "203.079373"
-xref: spec_2_neutral_loss_204_avge_mass "203.1925"
-xref: spec_2_neutral_loss_204_flag "false"
-xref: spec_2_neutral_loss_204_composition "HexNAc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "C"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Other glycosylation"
-xref: spec_3_neutral_loss_204_mono_mass "203.079373"
-xref: spec_3_neutral_loss_204_avge_mass "203.1925"
-xref: spec_3_neutral_loss_204_flag "false"
-xref: spec_3_neutral_loss_204_composition "HexNAc"
-xref: spec_3_neutral_loss_0_mono_mass "0"
-xref: spec_3_neutral_loss_0_avge_mass "0"
-xref: spec_3_neutral_loss_0_flag "false"
-xref: spec_3_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:44
-name: Farnesyl
-def: "Farnesylation." [PMID:15609361, RESID:AA0102, FindMod:FARN, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=44]
-xref: record_id "44"
-xref: delta_mono_mass "204.187801"
-xref: delta_avge_mass "204.3511"
-xref: delta_composition "H(24) C(15)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-16 15:11:38"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:45
-name: Myristoyl
-def: "Myristoylation." [RESID:AA0059, RESID:AA0307, RESID:AA0078, FindMod:MYRI, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=45]
-xref: record_id "45"
-xref: delta_mono_mass "210.198366"
-xref: delta_avge_mass "210.3556"
-xref: delta_composition "H(26) C(14) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-16 15:13:17"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "C"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:46
-name: PyridoxalPhosphate
-def: "Pyridoxal phosphate." [RESID:AA0119, FindMod:PLP, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=46]
-comment: The co-enzyme derivative of vitamin B6. Forms Schiff\'s bases of substrate amino acids during catalysis of transamination, decarboxylation and racemisation reactions.
-xref: record_id "46"
-xref: delta_mono_mass "229.014009"
-xref: delta_avge_mass "229.1266"
-xref: delta_composition "H(8) C(8) N O(5) P"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-16 15:35:42"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:47
-name: Palmitoyl
-def: "Palmitoylation." [RESID:AA0080, RESID:AA0079, RESID:AA0106, RESID:AA0077, FindMod:PALM, RESID:AA0339, RESID:AA0060, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=47]
-comment: Palmitoylation is a post-translational modification that consists in the addition of a 16 carbons fatty acid, palmitate, to a cysteine residue through the creation of a thioester link.
-xref: record_id "47"
-xref: delta_mono_mass "238.229666"
-xref: delta_avge_mass "238.4088"
-xref: delta_composition "H(30) C(16) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-16 15:38:43"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "S"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "T"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Post-translational"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "N-term"
-xref: spec_5_position "Protein N-term"
-xref: spec_5_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:48
-name: GeranylGeranyl
-def: "Geranyl-geranyl." [RESID:AA0104, PMID:15609361, FindMod:GERA, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=48]
-xref: record_id "48"
-xref: delta_mono_mass "272.250401"
-xref: delta_avge_mass "272.4681"
-xref: delta_composition "H(32) C(20)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-16 15:47:48"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:49
-name: Phosphopantetheine
-def: "Phosphopantetheine." [RESID:AA0150, FindMod:PPAN, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=49]
-comment: Protein which contains at least one phosphopantetheine as the prosthetic group. In acyl carrier proteins (ACP) for example, it serves as a \'swinging arm\' for the attachment of activated fatty acid and amino-acid groups.
-xref: record_id "49"
-xref: delta_mono_mass "340.085794"
-xref: delta_avge_mass "340.333"
-xref: delta_composition "H(21) C(11) N(2) O(6) P S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-16 16:00:24"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:50
-name: FAD
-def: "Flavin adenine dinucleotide." [RESID:AA0143, URL:http\://www.aw-bc.com/mathews/EF/FAD.GIF, RESID:AA0144, RESID:AA0145, RESID:AA0221, FindMod:FAD, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=50]
-xref: record_id "50"
-xref: delta_mono_mass "783.141486"
-xref: delta_avge_mass "783.5339"
-xref: delta_composition "H(31) C(27) N(9) O(15) P(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-16 17:16:18"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:51
-name: Tripalmitate
-def: "N-acyl diglyceride cysteine." [PMID:10356335, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=51]
-xref: record_id "51"
-xref: delta_mono_mass "788.725777"
-xref: delta_avge_mass "789.3049"
-xref: delta_composition "H(96) C(51) O(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2006-10-18 11:47:54"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Protein N-term"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:52
-name: Guanidinyl
-def: "Guanidination." [PMID:11821862, URL:http\://www.indiana.edu/~reillyjp/ASMS2001posters/beardsley_poster.pdf, PMID:11078590, PMID:11085420, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=52]
-comment: Specific for sidechain of lysine. Does not modify the N-termini except for glycine at a slower rate than the side chain of lysine.
-synonym: "homoarginine" RELATED []
-xref: record_id "52"
-xref: delta_mono_mass "42.021798"
-xref: delta_avge_mass "42.04"
-xref: delta_composition "H(2) C N(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2011-11-21 13:56:40"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:53
-name: HNE
-def: "4-hydroxynonenal (HNE)." [PMID:11327326, PMID:15276160, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=53]
-comment: A lipid-type modification. HNE forms a Michael addition product on Cysteine, Histidine and Lysines. Unusually, it doesn\'t replace a hydrogen on the amino acid side chain.
-xref: record_id "53"
-xref: delta_mono_mass "156.11503"
-xref: delta_avge_mass "156.2221"
-xref: delta_composition "H(16) C(9) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-08-19 19:17:11"
-xref: date_time_modified "2024-06-27 09:30:34"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "A"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Post-translational"
-xref: spec_4_misc_notes "GFAP from human brain tissues"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "L"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Post-translational"
-xref: spec_5_misc_notes "GFAP from human brain tissues"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "R"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:54
-name: Glucuronyl
-def: "Hexuronic acid." [PMID:7398618, RESID:AA0291, RESID:AA0058, URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hexa=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=54]
-comment: The addition of a sugar unit to a protein amino acid, e.g. the addition of glycan chains to proteins. Addition of glucuronic acid. Observed for N-term G.
-synonym: "glucuronosyl" RELATED []
-xref: record_id "54"
-xref: delta_mono_mass "176.032088"
-xref: delta_avge_mass "176.1241"
-xref: delta_composition "HexA"
-xref: username_of_poster "jcottrell"
-xref: group_of_poster "users"
-xref: date_time_posted "2002-10-01 21:36:48"
-xref: date_time_modified "2017-11-16 14:51:01"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Protein N-term"
-xref: spec_1_classification "Other glycosylation"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_177_mono_mass "176.032088"
-xref: spec_2_neutral_loss_177_avge_mass "176.1241"
-xref: spec_2_neutral_loss_177_flag "false"
-xref: spec_2_neutral_loss_177_composition "HexA"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_177_mono_mass "176.032088"
-xref: spec_2_neutral_loss_177_avge_mass "176.1241"
-xref: spec_2_neutral_loss_177_flag "false"
-xref: spec_2_neutral_loss_177_composition "HexA"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:55
-name: Glutathione
-def: "Glutathione disulfide." [PMID:3083866, PMID:8344916, RESID:AA0229, FindMod:GLUT, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=55]
-xref: record_id "55"
-xref: delta_mono_mass "305.068156"
-xref: delta_avge_mass "305.3076"
-xref: delta_composition "H(15) C(10) N(3) O(6) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2002-10-03 09:10:19"
-xref: date_time_modified "2006-10-16 15:51:52"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:56
-name: Acetyl:2H(3)
-def: "Acetate labeling reagent (N-term & K) (heavy form, +3amu)." [PMID:11857757, PMID:11999733, PMID:12175151, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=56]
-synonym: "N-trideuteriumacetoxy" RELATED []
-xref: record_id "56"
-xref: delta_mono_mass "45.029395"
-xref: delta_avge_mass "45.0552"
-xref: delta_composition "H(-1) 2H(3) C(2) O"
-xref: username_of_poster "penner"
-xref: group_of_poster "users"
-xref: date_time_posted "2002-10-16 16:41:56"
-xref: date_time_modified "2021-12-07 13:53:57"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "H"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "S"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "T"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Isotopic label"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "Y"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Isotopic label"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "N-term"
-xref: spec_7_position "Protein N-term"
-xref: spec_7_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:58
-name: Propionyl
-def: "Propionate labeling reagent light form (N-term & K)." [PMID:12175151, PMID:11999733, PMID:11857757, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=58]
-xref: record_id "58"
-xref: delta_mono_mass "56.026215"
-xref: delta_avge_mass "56.0633"
-xref: delta_composition "H(4) C(3) O"
-xref: username_of_poster "penner"
-xref: group_of_poster "users"
-xref: date_time_posted "2002-10-16 16:52:38"
-xref: date_time_modified "2021-12-07 13:54:44"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "S"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "T"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "N-term"
-xref: spec_5_position "Protein N-term"
-xref: spec_5_classification "Multiple"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:59
-name: Propionyl:13C(3)
-def: "Propionate labeling reagent heavy form (+3amu), N-term & K." [PMID:11999733, PMID:12175151, PMID:11857757, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=59]
-xref: record_id "59"
-xref: delta_mono_mass "59.036279"
-xref: delta_avge_mass "59.0412"
-xref: delta_composition "H(4) 13C(3) O"
-xref: username_of_poster "penner"
-xref: group_of_poster "users"
-xref: date_time_posted "2002-10-16 16:55:47"
-xref: date_time_modified "2021-12-07 13:55:08"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:60
-name: GIST-Quat
-def: "Quaternary amine labeling reagent light form (N-term & K)." [PMID:11857757, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=60]
-synonym: "N-(4-trimethylammoniumbutanoxy)-NHS" RELATED []
-xref: record_id "60"
-xref: delta_mono_mass "127.099714"
-xref: delta_avge_mass "127.1842"
-xref: delta_composition "H(13) C(7) N O"
-xref: username_of_poster "penner"
-xref: group_of_poster "users"
-xref: date_time_posted "2002-10-16 17:02:37"
-xref: date_time_modified "2021-12-07 13:56:41"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_neutral_loss_60_mono_mass "59.073499"
-xref: spec_1_neutral_loss_60_avge_mass "59.1103"
-xref: spec_1_neutral_loss_60_flag "false"
-xref: spec_1_neutral_loss_60_composition "H(9) C(3) N"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_2_neutral_loss_60_mono_mass "59.073499"
-xref: spec_2_neutral_loss_60_avge_mass "59.1103"
-xref: spec_2_neutral_loss_60_flag "false"
-xref: spec_2_neutral_loss_60_composition "H(9) C(3) N"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:61
-name: GIST-Quat:2H(3)
-def: "Quaternary amine labeling reagent heavy (+3amu) form, N-term & K." [PMID:11857757, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=61]
-xref: record_id "61"
-xref: delta_mono_mass "130.118544"
-xref: delta_avge_mass "130.2027"
-xref: delta_composition "H(10) 2H(3) C(7) N O"
-xref: username_of_poster "penner"
-xref: group_of_poster "users"
-xref: date_time_posted "2002-10-16 17:09:34"
-xref: date_time_modified "2021-12-07 13:57:03"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_neutral_loss_63_mono_mass "62.09233"
-xref: spec_1_neutral_loss_63_avge_mass "62.1287"
-xref: spec_1_neutral_loss_63_flag "false"
-xref: spec_1_neutral_loss_63_composition "H(6) 2H(3) C(3) N"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_2_neutral_loss_63_mono_mass "62.09233"
-xref: spec_2_neutral_loss_63_avge_mass "62.1287"
-xref: spec_2_neutral_loss_63_flag "false"
-xref: spec_2_neutral_loss_63_composition "H(6) 2H(3) C(3) N"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:62
-name: GIST-Quat:2H(6)
-def: "Quaternary amine labeling reagent heavy form (+6amu), N-term & K." [PMID:11857757, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=62]
-xref: record_id "62"
-xref: delta_mono_mass "133.137375"
-xref: delta_avge_mass "133.2212"
-xref: delta_composition "H(7) 2H(6) C(7) N O"
-xref: username_of_poster "penner"
-xref: group_of_poster "users"
-xref: date_time_posted "2002-10-16 17:12:27"
-xref: date_time_modified "2021-12-07 13:57:16"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_neutral_loss_66_mono_mass "65.11116"
-xref: spec_1_neutral_loss_66_avge_mass "65.1472"
-xref: spec_1_neutral_loss_66_flag "false"
-xref: spec_1_neutral_loss_66_composition "H(3) 2H(6) C(3) N"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_2_neutral_loss_66_mono_mass "65.11116"
-xref: spec_2_neutral_loss_66_avge_mass "65.1472"
-xref: spec_2_neutral_loss_66_flag "false"
-xref: spec_2_neutral_loss_66_composition "H(3) 2H(6) C(3) N"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:63
-name: GIST-Quat:2H(9)
-def: "Quaternary amine labeling reagent heavy form (+9amu), N-term & K." [PMID:11857757, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=63]
-xref: record_id "63"
-xref: delta_mono_mass "136.156205"
-xref: delta_avge_mass "136.2397"
-xref: delta_composition "H(4) 2H(9) C(7) N O"
-xref: username_of_poster "penner"
-xref: group_of_poster "users"
-xref: date_time_posted "2002-10-16 17:14:22"
-xref: date_time_modified "2021-12-07 13:57:28"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_neutral_loss_69_mono_mass "68.12999"
-xref: spec_1_neutral_loss_69_avge_mass "68.1657"
-xref: spec_1_neutral_loss_69_flag "false"
-xref: spec_1_neutral_loss_69_composition "2H(9) C(3) N"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_2_neutral_loss_69_mono_mass "68.12999"
-xref: spec_2_neutral_loss_69_avge_mass "68.1657"
-xref: spec_2_neutral_loss_69_flag "false"
-xref: spec_2_neutral_loss_69_composition "2H(9) C(3) N"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:64
-name: Succinyl
-def: "Succinic anhydride labeling reagent light form (N-term & K)." [RESID:AA0130, PMID:11857757, PMID:12175151, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=64]
-xref: record_id "64"
-xref: delta_mono_mass "100.016044"
-xref: delta_avge_mass "100.0728"
-xref: delta_composition "H(4) C(4) O(3)"
-xref: username_of_poster "penner"
-xref: group_of_poster "users"
-xref: date_time_posted "2002-10-16 17:17:07"
-xref: date_time_modified "2021-12-07 13:55:39"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:65
-name: Succinyl:2H(4)
-def: "Succinic anhydride labeling reagent, heavy form (+4amu, 4H2), N-term & K." [PMID:12175151, PMID:11857757, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=65]
-xref: record_id "65"
-xref: delta_mono_mass "104.041151"
-xref: delta_avge_mass "104.0974"
-xref: delta_composition "2H(4) C(4) O(3)"
-xref: username_of_poster "penner"
-xref: group_of_poster "users"
-xref: date_time_posted "2002-10-16 17:19:51"
-xref: date_time_modified "2021-12-07 13:56:27"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:66
-name: Succinyl:13C(4)
-def: "Succinic anhydride labeling reagent, heavy form (+4amu, 4C13), N-term & K." [PMID:12175151, PMID:11857757, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=66]
-xref: record_id "66"
-xref: delta_mono_mass "104.029463"
-xref: delta_avge_mass "104.0434"
-xref: delta_composition "H(4) 13C(4) O(3)"
-xref: username_of_poster "penner"
-xref: group_of_poster "users"
-xref: date_time_posted "2002-10-16 17:23:58"
-xref: date_time_modified "2021-12-07 13:56:08"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:89
-name: Iminobiotin
-def: "Iminobiotinylation." [PMID:9750125, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=89]
-xref: record_id "89"
-xref: delta_mono_mass "225.093583"
-xref: delta_avge_mass "225.3106"
-xref: delta_composition "H(15) C(10) N(3) O S"
-xref: username_of_poster "toppolzer"
-xref: group_of_poster "users"
-xref: date_time_posted "2002-11-25 16:01:48"
-xref: date_time_modified "2006-10-16 15:26:37"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:90
-name: ESP
-def: "ESP-Tag light d0." [URL:http\://www.wzw.tum.de/proteomik/forum2003/Posters-Abstracts.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=90]
-xref: record_id "90"
-xref: delta_mono_mass "338.177647"
-xref: delta_avge_mass "338.4682"
-xref: delta_composition "H(26) C(16) N(4) O(2) S"
-xref: username_of_poster "toppolzer"
-xref: group_of_poster "users"
-xref: date_time_posted "2002-11-25 16:12:50"
-xref: date_time_modified "2006-10-16 15:58:19"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:91
-name: ESP:2H(10)
-def: "ESP-Tag heavy d10." [URL:http\://www.wzw.tum.de/proteomik/forum2003/Posters-Abstracts.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=91]
-xref: record_id "91"
-xref: delta_mono_mass "348.240414"
-xref: delta_avge_mass "348.5299"
-xref: delta_composition "H(16) 2H(10) C(16) N(4) O(2) S"
-xref: username_of_poster "toppolzer"
-xref: group_of_poster "users"
-xref: date_time_posted "2002-11-25 16:18:58"
-xref: date_time_modified "2006-10-16 16:03:06"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:92
-name: NHS-LC-Biotin
-def: "NHS-LC-Biotin." [URL:http\://pubs.acs.org/doi/abs/10.1021/bi062142x, URL:http\://www.piercenet.com/Proteomics/browse.cfm?fldID=84EBE112-F871-4CA5-807F-47327153CFCB, URL:http\://www.piercenet.com/Products/Browse.cfm?fldID=8D38BA83-EFDC-421A-853F-E96EBA380612, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=92]
-synonym: "N-biotinyl-6-aminohexanoyl" RELATED []
-xref: record_id "92"
-xref: delta_mono_mass "339.161662"
-xref: delta_avge_mass "339.453"
-xref: delta_composition "H(25) C(16) N(3) O(3) S"
-xref: username_of_poster "toppolzer"
-xref: group_of_poster "users"
-xref: date_time_posted "2002-12-04 09:55:19"
-xref: date_time_modified "2015-05-07 10:57:59"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:93
-name: EDT-maleimide-PEO-biotin
-def: "EDT-maleimide-PEO-biotin." [URL:http\://www.piercenet.com/Products/Browse.cfm?fldID=01031005, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=93]
-xref: record_id "93"
-xref: delta_mono_mass "601.206246"
-xref: delta_avge_mass "601.8021"
-xref: delta_composition "H(39) C(25) N(5) O(6) S(3)"
-xref: username_of_poster "take"
-xref: group_of_poster "users"
-xref: date_time_posted "2002-12-27 09:08:56"
-xref: date_time_modified "2006-11-14 11:15:06"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:94
-name: IMID
-def: "IMID d0." [PMID:11746907, URL:http\://www.chem.agilent.com/cag/lystag.asp, URL:http\://www.chem.agilent.com/cag/other/IMTHUPO2003.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=94]
-synonym: "2-methoxy-4,5-dihydro-1H-imidazole derivative Lys imidazole" RELATED []
-xref: record_id "94"
-xref: delta_mono_mass "68.037448"
-xref: delta_avge_mass "68.0773"
-xref: delta_composition "H(4) C(3) N(2)"
-xref: username_of_poster "Liao"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-01-09 04:14:06"
-xref: date_time_modified "2006-10-16 10:33:45"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:95
-name: IMID:2H(4)
-def: "IMID d4." [URL:http\://www.chem.agilent.com/cag/lystag.asp, PMID:11746907, URL:http\://www.chem.agilent.com/cag/other/IMTHUPO2003.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=95]
-synonym: "2-methoxy-4,5-dihydro-1H-imidazole derivative" RELATED []
-xref: record_id "95"
-xref: delta_mono_mass "72.062555"
-xref: delta_avge_mass "72.1019"
-xref: delta_composition "2H(4) C(3) N(2)"
-xref: username_of_poster "Liao"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-01-09 04:15:25"
-xref: date_time_modified "2006-10-16 11:06:13"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:97
-name: Propionamide:2H(3)
-def: "Acrylamide d3." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=97]
-xref: record_id "97"
-xref: delta_mono_mass "74.055944"
-xref: delta_avge_mass "74.0964"
-xref: delta_composition "H(2) 2H(3) C(3) N O"
-xref: username_of_poster "Liao"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-01-14 08:10:30"
-xref: date_time_modified "2006-10-16 11:07:07"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:105
-name: ICAT-C
-def: "Applied Biosystems cleavable ICAT(TM) light." [URL:http\://www.chemsoc.org/exemplarchem/entries/2002/proteomics/icat.htm, URL:https\://products.appliedbiosystems.com/ab/en/US/adirect/ab?cmd=catNavigate2&catID=600902, URL:http\://docs.appliedbiosystems.com/pebiodocs/04333373.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=105]
-xref: record_id "105"
-xref: delta_mono_mass "227.126991"
-xref: delta_avge_mass "227.2603"
-xref: delta_composition "H(17) C(10) N(3) O(3)"
-xref: username_of_poster "tpjd2"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-01-27 10:27:11"
-xref: date_time_modified "2006-10-16 15:32:17"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:106
-name: ICAT-C:13C(9)
-def: "Applied Biosystems cleavable ICAT(TM) heavy." [URL:http\://docs.appliedbiosystems.com/pebiodocs/04333373.pdf, URL:https\://products.appliedbiosystems.com/ab/en/US/adirect/ab?cmd=catNavigate2&catID=600902, URL:http\://www.chemsoc.org/exemplarchem/entries/2002/proteomics/icat.htm, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=106]
-xref: record_id "106"
-xref: delta_mono_mass "236.157185"
-xref: delta_avge_mass "236.1942"
-xref: delta_composition "H(17) C 13C(9) N(3) O(3)"
-xref: username_of_poster "tpjd2"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-01-27 10:32:53"
-xref: date_time_modified "2006-10-16 15:34:14"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:107
-name: FormylMet
-def: "Addition of N-formyl met." [RESID:AA0021, PMID:10825024, PMID:8758896, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=107]
-xref: record_id "107"
-xref: delta_mono_mass "159.035399"
-xref: delta_avge_mass "159.2062"
-xref: delta_composition "H(9) C(6) N O(2) S"
-xref: username_of_poster "jphilip"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-01-27 18:24:14"
-xref: date_time_modified "2006-10-16 14:08:15"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Protein N-term"
-xref: spec_1_classification "Pre-translational"
-xref: spec_1_misc_notes "only with Listeria monocytogenes (gram-positive bacteria)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:108
-name: Nethylmaleimide
-def: "N-ethylmaleimide on cysteines." [URL:http\://www.chemistry.ucsc.edu/~fink/231/Image118.gif, PMID:12777388, PMID:11813307, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=108]
-synonym: "CysNEM" RELATED []
-xref: record_id "108"
-xref: delta_mono_mass "125.047679"
-xref: delta_avge_mass "125.1253"
-xref: delta_composition "H(7) C(6) N O(2)"
-xref: username_of_poster "Pflieger"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-01-30 09:52:51"
-xref: date_time_modified "2006-10-16 13:36:10"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:112
-name: OxLysBiotinRed
-def: "Oxidized lysine biotinylated with biotin-LC-hydrazide, reduced." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=112]
-xref: record_id "112"
-xref: delta_mono_mass "354.172562"
-xref: delta_avge_mass "354.4676"
-xref: delta_composition "H(26) C(16) N(4) O(3) S"
-xref: username_of_poster "S_Lee"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-02-21 00:53:43"
-xref: date_time_modified "2006-11-14 12:10:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:113
-name: OxLysBiotin
-def: "Oxidized lysine biotinylated with biotin-LC-hydrazide." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=113]
-xref: record_id "113"
-xref: delta_mono_mass "352.156911"
-xref: delta_avge_mass "352.4518"
-xref: delta_composition "H(24) C(16) N(4) O(3) S"
-xref: username_of_poster "S_Lee"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-02-21 01:25:11"
-xref: date_time_modified "2006-11-14 12:10:53"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:114
-name: OxProBiotinRed
-def: "Oxidized proline biotinylated with biotin-LC-hydrazide, reduced." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=114]
-xref: record_id "114"
-xref: delta_mono_mass "371.199111"
-xref: delta_avge_mass "371.4982"
-xref: delta_composition "H(29) C(16) N(5) O(3) S"
-xref: username_of_poster "S_Lee"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-02-21 01:34:28"
-xref: date_time_modified "2006-11-14 12:11:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:115
-name: OxProBiotin
-def: "Oxidized Proline biotinylated with biotin-LC-hydrazide." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=115]
-xref: record_id "115"
-xref: delta_mono_mass "369.183461"
-xref: delta_avge_mass "369.4823"
-xref: delta_composition "H(27) C(16) N(5) O(3) S"
-xref: username_of_poster "S_Lee"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-02-21 01:35:44"
-xref: date_time_modified "2006-11-14 12:11:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:116
-name: OxArgBiotin
-def: "Oxidized arginine biotinylated with biotin-LC-hydrazide." [URL:http\://www.piercenet.com/Proteomics/browse.cfm?fldID=84EBE112-F871-4CA5-807F-47327153CFCB, URL:http\://themedicalbiochemistrypage.org/nitrogen-metabolism.html, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=116]
-xref: record_id "116"
-xref: delta_mono_mass "310.135113"
-xref: delta_avge_mass "310.4118"
-xref: delta_composition "H(22) C(15) N(2) O(3) S"
-xref: username_of_poster "S_Lee"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-02-21 01:41:19"
-xref: date_time_modified "2011-07-18 11:34:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:117
-name: OxArgBiotinRed
-def: "Oxidized arginine biotinylated with biotin-LC-hydrazide, reduced." [URL:http\://www.piercenet.com/Proteomics/browse.cfm?fldID=84EBE112-F871-4CA5-807F-47327153CFCB, URL:http\://themedicalbiochemistrypage.org/nitrogen-metabolism.html, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=117]
-xref: record_id "117"
-xref: delta_mono_mass "312.150763"
-xref: delta_avge_mass "312.4277"
-xref: delta_composition "H(24) C(15) N(2) O(3) S"
-xref: username_of_poster "S_Lee"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-02-21 01:43:00"
-xref: date_time_modified "2011-07-18 11:33:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:118
-name: EDT-iodoacetyl-PEO-biotin
-def: "EDT-iodo-PEO-biotin." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=118]
-xref: record_id "118"
-xref: delta_mono_mass "490.174218"
-xref: delta_avge_mass "490.7034"
-xref: delta_composition "H(34) C(20) N(4) O(4) S(3)"
-xref: username_of_poster "take"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-02-24 07:18:42"
-xref: date_time_modified "2006-10-16 17:01:15"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:119
-name: IBTP
-def: "Thio Ether Formation - BTP Adduct." [PMID:11861642, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=119]
-xref: record_id "119"
-xref: delta_mono_mass "316.138088"
-xref: delta_avge_mass "316.3759"
-xref: delta_composition "H(21) C(22) P"
-xref: username_of_poster "MRCDunn"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-03-13 09:36:40"
-xref: date_time_modified "2006-10-16 15:52:42"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:121
-name: GG
-def: "Ubiquitinylation residue." [PMID:34673284, URL:http\://www.nottingham.ac.uk/biochemcourses/students/ub/ubindex.html, PMID:15055197, PMID:24782567, PMID:28884683, PMID:12872131, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=121]
-comment: The two glycine residues left on ubiquitinylated lysine after tryptic digestion.
-synonym: "SUMOylation leaving GG tag glycineglycine" RELATED []
-xref: record_id "121"
-xref: delta_mono_mass "114.042927"
-xref: delta_avge_mass "114.1026"
-xref: delta_composition "H(6) C(4) N(2) O(2)"
-xref: username_of_poster "gielbert"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-04-30 13:32:37"
-xref: date_time_modified "2023-09-27 10:44:25"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Other"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Other"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "C"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Other"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "N-term"
-xref: spec_5_position "Protein N-term"
-xref: spec_5_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:122
-name: Formyl
-def: "Formylation." [RESID:AA0211, PMID:15799070, RESID:AA0021, FindMod:FORM, RESID:AA0384, RESID:AA0057, RESID:AA0384, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=122]
-xref: record_id "122"
-xref: delta_mono_mass "27.994915"
-xref: delta_avge_mass "28.0101"
-xref: delta_composition "C O"
-xref: username_of_poster "pnacman"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-05-01 13:28:36"
-xref: date_time_modified "2006-11-14 12:01:57"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_misc_notes "Can occur under CNBr cleavage conditions (70% HCOOH)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Artefact"
-xref: spec_2_misc_notes "Can occur under CNBr cleavage conditions (70% HCOOH)"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "S"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Artefact"
-xref: spec_3_misc_notes "Can occur under CNBr cleavage conditions (70% HCOOH)"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "T"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Artefact"
-xref: spec_4_misc_notes "Can occur under CNBr cleavage conditions (70% HCOOH)"
-xref: spec_5_group "5"
-xref: spec_5_hidden "0"
-xref: spec_5_site "N-term"
-xref: spec_5_position "Protein N-term"
-xref: spec_5_classification "Post-translational"
-xref: spec_5_misc_notes "A protein in which either the N-terminal N-formylmethionine has not been processed by the methionyl-tRNA formyltransferase or which is posttranslationally modified by the attachment of at least one formyl group."
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:123
-name: ICAT-H
-def: "N-iodoacetyl, p-chlorobenzyl-12C6-glucamine." [PMID:12185208, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=123]
-synonym: "Harbury glyco-ICAT C12" RELATED []
-xref: record_id "123"
-xref: delta_mono_mass "345.097915"
-xref: delta_avge_mass "345.7754"
-xref: delta_composition "H(20) C(15) N O(6) Cl"
-xref: username_of_poster "allis"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-05-07 19:54:20"
-xref: date_time_modified "2006-10-16 16:02:00"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:124
-name: ICAT-H:13C(6)
-def: "N-iodoacetyl, p-chlorobenzyl-13C6-glucamine." [PMID:12185208, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=124]
-synonym: "Harbury glyco-ICAT C13" RELATED []
-xref: record_id "124"
-xref: delta_mono_mass "351.118044"
-xref: delta_avge_mass "351.7313"
-xref: delta_composition "H(20) C(9) 13C(6) N O(6) Cl"
-xref: username_of_poster "allis"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-05-07 19:56:12"
-xref: date_time_modified "2006-10-16 16:04:02"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:126
-name: Xlink:DTSSP[88]
-def: "Cleaved and reduced DSP/DTSSP crosslinker." [URL:https\://tools.thermofisher.com/content/sfs/manuals/MAN0011280_DTSSP_DSP_UG.pdf, PMID:322714, PMID:3155470, PMID:957432, PMID:8457554, PMID:11710128, PMID:1262347, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=126]
-comment: Can also be the product of reaction with EZ-Link Sulfo-NHS-SS-Biotin (Sulfosuccinimidyl 2-(biotinamido)-ethyl-1, 3-dithiopropionate) followed by reduction with DTT.
-synonym: "(Was Thioacyl)" RELATED []
-xref: record_id "126"
-xref: delta_mono_mass "87.998285"
-xref: delta_avge_mass "88.1283"
-xref: delta_composition "H(4) C(3) O S"
-xref: username_of_poster "rabah"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-06-05 13:38:19"
-xref: date_time_modified "2017-08-18 17:03:05"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:127
-name: Fluoro
-def: "Fluorination." [PMID:1093385, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=127]
-xref: record_id "127"
-xref: delta_mono_mass "17.990578"
-xref: delta_avge_mass "17.9905"
-xref: delta_composition "H(-1) F"
-xref: username_of_poster "jschulte"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-06-19 19:54:25"
-xref: date_time_modified "2012-11-20 11:56:44"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Non-standard residue"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "W"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Non-standard residue"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Non-standard residue"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "A"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:128
-name: Fluorescein
-def: "5-Iodoacetamidofluorescein (Molecular Probe, Eugene, OR)." [PMID:3578767, PMID:3311742, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=128]
-xref: record_id "128"
-xref: delta_mono_mass "387.074287"
-xref: delta_avge_mass "387.3417"
-xref: delta_composition "H(13) C(22) N O(6)"
-xref: username_of_poster "Philip"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-06-25 02:58:18"
-xref: date_time_modified "2017-11-01 12:11:48"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:129
-name: Iodo
-def: "Iodination." [PMID:2026710, PMID:15627961, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=129]
-xref: record_id "129"
-xref: delta_mono_mass "125.896648"
-xref: delta_avge_mass "125.8965"
-xref: delta_composition "H(-1) I"
-xref: username_of_poster "brettsp"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-07-10 15:43:17"
-xref: date_time_modified "2006-10-16 13:38:03"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:130
-name: Diiodo
-def: "Di-Iodination." [PMID:15627961, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=130]
-xref: record_id "130"
-xref: delta_mono_mass "251.793296"
-xref: delta_avge_mass "251.7931"
-xref: delta_composition "H(-2) I(2)"
-xref: username_of_poster "brettsp"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-07-10 15:49:42"
-xref: date_time_modified "2011-11-21 13:23:20"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:131
-name: Triiodo
-def: "Tri-Iodination." [PMID:2026710, PMID:15627961, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=131]
-xref: record_id "131"
-xref: delta_mono_mass "377.689944"
-xref: delta_avge_mass "377.6896"
-xref: delta_composition "H(-3) I(3)"
-xref: username_of_poster "brettsp"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-07-10 15:51:32"
-xref: date_time_modified "2006-10-16 16:36:49"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:134
-name: Myristoleyl
-def: "(cis-delta 5)-tetradecaenoyl." [PMID:1326520, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=134]
-comment: Found on vision signal transduction proteins.
-synonym: "myristoyl with one double bond C14:1 acylation" RELATED []
-xref: record_id "134"
-xref: delta_mono_mass "208.182715"
-xref: delta_avge_mass "208.3398"
-xref: delta_composition "H(24) C(14) O"
-xref: username_of_poster "tomneubert"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-07-18 21:30:51"
-xref: date_time_modified "2006-10-16 15:11:18"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Protein N-term"
-xref: spec_1_classification "Co-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:135
-name: Myristoyl+Delta:H(-4)
-def: "(cis,cis-delta 5, delta 8)-tetradecadienoyl." [PMID:1326520, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=135]
-comment: Found on vision signal transduction proteins.
-synonym: "myristoyl with 2 double bonds C14:2 fatty acylation" RELATED []
-xref: record_id "135"
-xref: delta_mono_mass "206.167065"
-xref: delta_avge_mass "206.3239"
-xref: delta_composition "H(22) C(14) O"
-xref: username_of_poster "tomneubert"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-07-18 21:36:44"
-xref: date_time_modified "2006-10-16 15:10:51"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Protein N-term"
-xref: spec_1_classification "Co-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:136
-name: Benzoyl
-def: "Labeling reagent light form (N-term & K)." [PMID:15456300, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=136]
-xref: record_id "136"
-xref: delta_mono_mass "104.026215"
-xref: delta_avge_mass "104.1061"
-xref: delta_composition "H(4) C(7) O"
-xref: username_of_poster "samirjulka"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-07-31 22:24:05"
-xref: date_time_modified "2006-10-16 12:41:22"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:137
-name: Hex(5)HexNAc(2)
-def: "M5/Man5." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=5&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=137]
-comment: Core structure of high-mannose N-linked oligosaccharides.
-synonym: "N-linked glycan core" RELATED []
-xref: record_id "137"
-xref: delta_mono_mass "1216.422863"
-xref: delta_avge_mass "1217.088"
-xref: delta_composition "Hex(5) HexNAc(2)"
-xref: username_of_poster "tpjd2"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-08-06 11:31:37"
-xref: date_time_modified "2020-08-02 11:50:32"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1217_mono_mass "1216.422863"
-xref: spec_1_neutral_loss_1217_avge_mass "1217.088"
-xref: spec_1_neutral_loss_1217_flag "false"
-xref: spec_1_neutral_loss_1217_composition "Hex(5) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:139
-name: Dansyl
-def: "5-dimethylaminonaphthalene-1-sulfonyl." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=139]
-xref: record_id "139"
-xref: delta_mono_mass "233.051049"
-xref: delta_avge_mass "233.2862"
-xref: delta_composition "H(11) C(12) N O(2) S"
-xref: username_of_poster "allis"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-08-19 02:51:24"
-xref: date_time_modified "2006-10-16 15:36:09"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:140
-name: a-type-ion
-def: "ISD a-series (C-Term)." [PMID:14588022, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=140]
-comment: MS/MS experiments of mass spectrometric a-ions (MS^3) can be used for protein identification by library searching. T3-sequencing is such a technique (see reference). Search engines must recognize this \'virtual modification\' for this purpose.
-synonym: "Decarboxylation of C-terminus as reaction inside the mass spectrometer" RELATED []
-xref: record_id "140"
-xref: delta_mono_mass "-46.005479"
-xref: delta_avge_mass "-46.0254"
-xref: delta_composition "H(-2) C(-1) O(-2)"
-xref: username_of_poster "suckau"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-09-02 16:17:09"
-xref: date_time_modified "2010-06-08 14:19:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Any C-term"
-xref: spec_1_classification "Other"
-xref: spec_1_misc_notes "Virtual Modification for MS/MS of a-type ions corrected by subtraction of a further -O at 8.6.2010"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:141
-name: Amidine
-def: "Amidination of lysines or N-terminal amines with methyl acetimidate." [URL:http\://www.indiana.edu/~reillyjp/ASMS2004/janecki_Ext-Abs%20Amidination.pdf, PMID:12643539, PMID:6273432, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=141]
-xref: record_id "141"
-xref: delta_mono_mass "41.026549"
-xref: delta_avge_mass "41.0519"
-xref: delta_composition "H(3) C(2) N"
-xref: username_of_poster "pnacman"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-09-25 11:04:41"
-xref: date_time_modified "2006-10-15 18:32:25"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:142
-name: HexNAc(1)dHex(1)
-def: "HexNAc1dHex1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=142]
-xref: record_id "142"
-xref: delta_mono_mass "349.137281"
-xref: delta_avge_mass "349.3337"
-xref: delta_composition "dHex HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:28:45"
-xref: date_time_modified "2015-05-05 10:49:49"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_350_mono_mass "349.137281"
-xref: spec_1_neutral_loss_350_avge_mass "349.3337"
-xref: spec_1_neutral_loss_350_flag "false"
-xref: spec_1_neutral_loss_350_composition "dHex HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_350_mono_mass "349.137281"
-xref: spec_2_neutral_loss_350_avge_mass "349.3337"
-xref: spec_2_neutral_loss_350_flag "false"
-xref: spec_2_neutral_loss_350_composition "dHex HexNAc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_350_mono_mass "349.137281"
-xref: spec_2_neutral_loss_350_avge_mass "349.3337"
-xref: spec_2_neutral_loss_350_flag "false"
-xref: spec_2_neutral_loss_350_composition "dHex HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:143
-name: HexNAc(2)
-def: "HexNAc2." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=143]
-xref: record_id "143"
-xref: delta_mono_mass "406.158745"
-xref: delta_avge_mass "406.385"
-xref: delta_composition "HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:37:55"
-xref: date_time_modified "2015-05-05 10:50:08"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_407_mono_mass "406.158745"
-xref: spec_1_neutral_loss_407_avge_mass "406.385"
-xref: spec_1_neutral_loss_407_flag "false"
-xref: spec_1_neutral_loss_407_composition "HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_407_mono_mass "406.158745"
-xref: spec_2_neutral_loss_407_avge_mass "406.385"
-xref: spec_2_neutral_loss_407_flag "false"
-xref: spec_2_neutral_loss_407_composition "HexNAc(2)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_407_mono_mass "406.158745"
-xref: spec_2_neutral_loss_407_avge_mass "406.385"
-xref: spec_2_neutral_loss_407_flag "false"
-xref: spec_2_neutral_loss_407_composition "HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:144
-name: Hex(3)
-def: "Hex3." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=144]
-xref: record_id "144"
-xref: delta_mono_mass "486.158471"
-xref: delta_avge_mass "486.4218"
-xref: delta_composition "Hex(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:39:30"
-xref: date_time_modified "2015-05-05 10:52:04"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_487_mono_mass "486.158471"
-xref: spec_1_neutral_loss_487_avge_mass "486.4218"
-xref: spec_1_neutral_loss_487_flag "false"
-xref: spec_1_neutral_loss_487_composition "Hex(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_487_mono_mass "486.158471"
-xref: spec_2_neutral_loss_487_avge_mass "486.4218"
-xref: spec_2_neutral_loss_487_flag "false"
-xref: spec_2_neutral_loss_487_composition "Hex(3)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_487_mono_mass "486.158471"
-xref: spec_2_neutral_loss_487_avge_mass "486.4218"
-xref: spec_2_neutral_loss_487_flag "false"
-xref: spec_2_neutral_loss_487_composition "Hex(3)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:145
-name: HexNAc(1)dHex(2)
-def: "HexNAc1dHex2." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=145]
-xref: record_id "145"
-xref: delta_mono_mass "495.19519"
-xref: delta_avge_mass "495.4749"
-xref: delta_composition "dHex(2) HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:40:57"
-xref: date_time_modified "2015-05-01 15:19:51"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_496_mono_mass "495.19519"
-xref: spec_1_neutral_loss_496_avge_mass "495.4749"
-xref: spec_1_neutral_loss_496_flag "false"
-xref: spec_1_neutral_loss_496_composition "dHex(2) HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:146
-name: Hex(1)HexNAc(1)dHex(1)
-def: "Hex1HexNAc1dHex1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=146]
-xref: record_id "146"
-xref: delta_mono_mass "511.190105"
-xref: delta_avge_mass "511.4743"
-xref: delta_composition "dHex Hex HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:42:27"
-xref: date_time_modified "2015-05-05 10:52:59"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_512_mono_mass "511.190105"
-xref: spec_1_neutral_loss_512_avge_mass "511.4743"
-xref: spec_1_neutral_loss_512_flag "false"
-xref: spec_1_neutral_loss_512_composition "dHex Hex HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_512_mono_mass "511.190105"
-xref: spec_2_neutral_loss_512_avge_mass "511.4743"
-xref: spec_2_neutral_loss_512_flag "false"
-xref: spec_2_neutral_loss_512_composition "dHex Hex HexNAc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_512_mono_mass "511.190105"
-xref: spec_2_neutral_loss_512_avge_mass "511.4743"
-xref: spec_2_neutral_loss_512_flag "false"
-xref: spec_2_neutral_loss_512_composition "dHex Hex HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:147
-name: HexNAc(2)dHex(1)
-def: "HexNAc2dHex1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=147]
-xref: record_id "147"
-xref: delta_mono_mass "552.216654"
-xref: delta_avge_mass "552.5262"
-xref: delta_composition "dHex HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:44:18"
-xref: date_time_modified "2015-05-01 15:23:32"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_553_mono_mass "552.216654"
-xref: spec_1_neutral_loss_553_avge_mass "552.5262"
-xref: spec_1_neutral_loss_553_flag "false"
-xref: spec_1_neutral_loss_553_composition "dHex HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:148
-name: Hex(1)HexNAc(2)
-def: "Hex1HexNAc2." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=148]
-xref: record_id "148"
-xref: delta_mono_mass "568.211569"
-xref: delta_avge_mass "568.5256"
-xref: delta_composition "Hex HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:48:18"
-xref: date_time_modified "2015-05-05 10:46:08"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_569_mono_mass "568.211569"
-xref: spec_1_neutral_loss_569_avge_mass "568.5256"
-xref: spec_1_neutral_loss_569_flag "false"
-xref: spec_1_neutral_loss_569_composition "Hex HexNAc(2)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_569_mono_mass "568.211569"
-xref: spec_2_neutral_loss_569_avge_mass "568.5256"
-xref: spec_2_neutral_loss_569_flag "false"
-xref: spec_2_neutral_loss_569_composition "Hex HexNAc(2)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_569_mono_mass "568.211569"
-xref: spec_2_neutral_loss_569_avge_mass "568.5256"
-xref: spec_2_neutral_loss_569_flag "false"
-xref: spec_2_neutral_loss_569_composition "Hex HexNAc(2)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:149
-name: Hex(1)HexNAc(1)NeuAc(1)
-def: "Hex1HexNAc1NeuAc1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=1&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=149]
-xref: record_id "149"
-xref: delta_mono_mass "656.227613"
-xref: delta_avge_mass "656.5877"
-xref: delta_composition "Hex HexNAc NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:51:19"
-xref: date_time_modified "2015-05-01 15:25:10"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_657_mono_mass "656.227613"
-xref: spec_1_neutral_loss_657_avge_mass "656.5877"
-xref: spec_1_neutral_loss_657_flag "false"
-xref: spec_1_neutral_loss_657_composition "Hex HexNAc NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_657_mono_mass "656.227613"
-xref: spec_2_neutral_loss_657_avge_mass "656.5877"
-xref: spec_2_neutral_loss_657_flag "false"
-xref: spec_2_neutral_loss_657_composition "Hex HexNAc NeuAc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_657_mono_mass "656.227613"
-xref: spec_2_neutral_loss_657_avge_mass "656.5877"
-xref: spec_2_neutral_loss_657_flag "false"
-xref: spec_2_neutral_loss_657_composition "Hex HexNAc NeuAc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:150
-name: HexNAc(2)dHex(2)
-def: "HexNAc2dHex2." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=150]
-xref: record_id "150"
-xref: delta_mono_mass "698.274563"
-xref: delta_avge_mass "698.6674"
-xref: delta_composition "dHex(2) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:52:36"
-xref: date_time_modified "2015-05-01 15:25:48"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_699_mono_mass "698.274563"
-xref: spec_1_neutral_loss_699_avge_mass "698.6674"
-xref: spec_1_neutral_loss_699_flag "false"
-xref: spec_1_neutral_loss_699_composition "dHex(2) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:151
-name: Hex(1)HexNAc(2)Pent(1)
-def: "Hex1HexNAc2Pent1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?pent=1&hex=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=151]
-xref: record_id "151"
-xref: delta_mono_mass "700.253828"
-xref: delta_avge_mass "700.6403"
-xref: delta_composition "Pent Hex HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:53:29"
-xref: date_time_modified "2015-05-01 15:26:17"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_701_mono_mass "700.253828"
-xref: spec_1_neutral_loss_701_avge_mass "700.6403"
-xref: spec_1_neutral_loss_701_flag "false"
-xref: spec_1_neutral_loss_701_composition "Pent Hex HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:152
-name: Hex(1)HexNAc(2)dHex(1)
-def: "Hex1HexNAc2dHex1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=152]
-xref: record_id "152"
-xref: delta_mono_mass "714.269478"
-xref: delta_avge_mass "714.6668"
-xref: delta_composition "dHex Hex HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:54:18"
-xref: date_time_modified "2015-05-05 16:20:33"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_715_mono_mass "714.269478"
-xref: spec_1_neutral_loss_715_avge_mass "714.6668"
-xref: spec_1_neutral_loss_715_flag "false"
-xref: spec_1_neutral_loss_715_composition "dHex Hex HexNAc(2)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_715_mono_mass "714.269478"
-xref: spec_2_neutral_loss_715_avge_mass "714.6668"
-xref: spec_2_neutral_loss_715_flag "false"
-xref: spec_2_neutral_loss_715_composition "dHex Hex HexNAc(2)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_715_mono_mass "714.269478"
-xref: spec_2_neutral_loss_715_avge_mass "714.6668"
-xref: spec_2_neutral_loss_715_flag "false"
-xref: spec_2_neutral_loss_715_composition "dHex Hex HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:153
-name: Hex(2)HexNAc(2)
-def: "Hex2HexNAc2." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=153]
-xref: record_id "153"
-xref: delta_mono_mass "730.264392"
-xref: delta_avge_mass "730.6662"
-xref: delta_composition "Hex(2) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:55:08"
-xref: date_time_modified "2015-05-05 16:22:13"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_731_mono_mass "730.264392"
-xref: spec_1_neutral_loss_731_avge_mass "730.6662"
-xref: spec_1_neutral_loss_731_flag "false"
-xref: spec_1_neutral_loss_731_composition "Hex(2) HexNAc(2)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_731_mono_mass "730.264392"
-xref: spec_2_neutral_loss_731_avge_mass "730.6662"
-xref: spec_2_neutral_loss_731_flag "false"
-xref: spec_2_neutral_loss_731_composition "Hex(2) HexNAc(2)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_731_mono_mass "730.264392"
-xref: spec_2_neutral_loss_731_avge_mass "730.6662"
-xref: spec_2_neutral_loss_731_flag "false"
-xref: spec_2_neutral_loss_731_composition "Hex(2) HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:154
-name: Hex(3)HexNAc(1)Pent(1)
-def: "Hex3HexNAc1Pent1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?pent=1&hex=3&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=154]
-xref: record_id "154"
-xref: delta_mono_mass "821.280102"
-xref: delta_avge_mass "821.7289"
-xref: delta_composition "Pent Hex(3) HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:56:02"
-xref: date_time_modified "2015-05-01 15:29:31"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_822_mono_mass "821.280102"
-xref: spec_1_neutral_loss_822_avge_mass "821.7289"
-xref: spec_1_neutral_loss_822_flag "false"
-xref: spec_1_neutral_loss_822_composition "Pent Hex(3) HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:155
-name: Hex(1)HexNAc(2)dHex(1)Pent(1)
-def: "Hex1HexNAc2dHex1Pent1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?pent=1&dhex=1&hex=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=155]
-xref: record_id "155"
-xref: delta_mono_mass "846.311736"
-xref: delta_avge_mass "846.7815"
-xref: delta_composition "Pent dHex Hex HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:57:01"
-xref: date_time_modified "2015-05-01 15:29:55"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_847_mono_mass "846.311736"
-xref: spec_1_neutral_loss_847_avge_mass "846.7815"
-xref: spec_1_neutral_loss_847_flag "false"
-xref: spec_1_neutral_loss_847_composition "Pent dHex Hex HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:156
-name: Hex(1)HexNAc(2)dHex(2)
-def: "Hex1HexNAc2dHex2." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=156]
-xref: record_id "156"
-xref: delta_mono_mass "860.327386"
-xref: delta_avge_mass "860.808"
-xref: delta_composition "dHex(2) Hex HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:57:52"
-xref: date_time_modified "2015-05-05 16:24:22"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_861_mono_mass "860.327386"
-xref: spec_1_neutral_loss_861_avge_mass "860.808"
-xref: spec_1_neutral_loss_861_flag "false"
-xref: spec_1_neutral_loss_861_composition "dHex(2) Hex HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_861_mono_mass "860.327386"
-xref: spec_2_neutral_loss_861_avge_mass "860.808"
-xref: spec_2_neutral_loss_861_flag "false"
-xref: spec_2_neutral_loss_861_composition "dHex(2) Hex HexNAc(2)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_861_mono_mass "860.327386"
-xref: spec_2_neutral_loss_861_avge_mass "860.808"
-xref: spec_2_neutral_loss_861_flag "false"
-xref: spec_2_neutral_loss_861_composition "dHex(2) Hex HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:157
-name: Hex(2)HexNAc(2)Pent(1)
-def: "Hex2HexNAc2Pent1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?pent=1&hex=2&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=157]
-xref: record_id "157"
-xref: delta_mono_mass "862.306651"
-xref: delta_avge_mass "862.7809"
-xref: delta_composition "Pent Hex(2) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:58:38"
-xref: date_time_modified "2015-05-01 15:30:54"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_863_mono_mass "862.306651"
-xref: spec_1_neutral_loss_863_avge_mass "862.7809"
-xref: spec_1_neutral_loss_863_flag "false"
-xref: spec_1_neutral_loss_863_composition "Pent Hex(2) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:158
-name: Hex(2)HexNAc(2)dHex(1)
-def: "Hex2HexNAc2dHex1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=2&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=158]
-xref: record_id "158"
-xref: delta_mono_mass "876.322301"
-xref: delta_avge_mass "876.8074"
-xref: delta_composition "dHex Hex(2) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:59:18"
-xref: date_time_modified "2015-05-05 16:26:14"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_877_mono_mass "876.322301"
-xref: spec_1_neutral_loss_877_avge_mass "876.8074"
-xref: spec_1_neutral_loss_877_flag "false"
-xref: spec_1_neutral_loss_877_composition "dHex Hex(2) HexNAc(2)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_877_mono_mass "876.322301"
-xref: spec_2_neutral_loss_877_avge_mass "876.8074"
-xref: spec_2_neutral_loss_877_flag "false"
-xref: spec_2_neutral_loss_877_composition "dHex Hex(2) HexNAc(2)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_877_mono_mass "876.322301"
-xref: spec_2_neutral_loss_877_avge_mass "876.8074"
-xref: spec_2_neutral_loss_877_flag "false"
-xref: spec_2_neutral_loss_877_composition "dHex Hex(2) HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:159
-name: Hex(3)HexNAc(2)
-def: "M3/Man3." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=159]
-synonym: "chitobiose core" RELATED []
-xref: record_id "159"
-xref: delta_mono_mass "892.317216"
-xref: delta_avge_mass "892.8068"
-xref: delta_composition "Hex(3) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 12:59:59"
-xref: date_time_modified "2020-08-02 11:51:23"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_893_mono_mass "892.317216"
-xref: spec_1_neutral_loss_893_avge_mass "892.8068"
-xref: spec_1_neutral_loss_893_flag "false"
-xref: spec_1_neutral_loss_893_composition "Hex(3) HexNAc(2)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_893_mono_mass "892.317216"
-xref: spec_2_neutral_loss_893_avge_mass "892.8068"
-xref: spec_2_neutral_loss_893_flag "false"
-xref: spec_2_neutral_loss_893_composition "Hex(3) HexNAc(2)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_893_mono_mass "892.317216"
-xref: spec_2_neutral_loss_893_avge_mass "892.8068"
-xref: spec_2_neutral_loss_893_flag "false"
-xref: spec_2_neutral_loss_893_composition "Hex(3) HexNAc(2)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:160
-name: Hex(1)HexNAc(1)NeuAc(2)
-def: "Hex HexNAc NeuAc(2) ---OR--- Hex HexNAc(3) HexA." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=1&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=160]
-xref: record_id "160"
-xref: delta_mono_mass "947.323029"
-xref: delta_avge_mass "947.8423"
-xref: delta_composition "Hex HexNAc NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 13:01:06"
-xref: date_time_modified "2017-11-17 11:43:49"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_948_mono_mass "947.323029"
-xref: spec_1_neutral_loss_948_avge_mass "947.8423"
-xref: spec_1_neutral_loss_948_flag "false"
-xref: spec_1_neutral_loss_948_composition "Hex HexNAc NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_948_mono_mass "947.323029"
-xref: spec_2_neutral_loss_948_avge_mass "947.8423"
-xref: spec_2_neutral_loss_948_flag "false"
-xref: spec_2_neutral_loss_948_composition "Hex HexNAc NeuAc(2)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_948_mono_mass "947.323029"
-xref: spec_2_neutral_loss_948_avge_mass "947.8423"
-xref: spec_2_neutral_loss_948_flag "false"
-xref: spec_2_neutral_loss_948_composition "Hex HexNAc NeuAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:161
-name: Hex(3)HexNAc(2)Phos(1)
-def: "Hex(3) HexNAc(2) Phos." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=1&hex=3&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=161]
-xref: record_id "161"
-xref: delta_mono_mass "972.283547"
-xref: delta_avge_mass "972.7867"
-xref: delta_composition "H O(3) P Hex(3) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2003-09-29 13:02:02"
-xref: date_time_modified "2015-05-06 09:48:32"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_973_mono_mass "972.283547"
-xref: spec_1_neutral_loss_973_avge_mass "972.7867"
-xref: spec_1_neutral_loss_973_flag "false"
-xref: spec_1_neutral_loss_973_composition "H O(3) P Hex(3) HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:162
-name: Delta:S(-1)Se(1)
-def: "Selenium replaces sulfur." [RESID:AA0022, PMID:12148805, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=162]
-xref: record_id "162"
-xref: delta_mono_mass "47.944449"
-xref: delta_avge_mass "46.895"
-xref: delta_composition "S(-1) Se"
-xref: username_of_poster "pnacman"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-10-14 11:24:28"
-xref: date_time_modified "2012-03-09 11:23:23"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Non-standard residue"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Non-standard residue"
-xref: spec_2_misc_notes "Selenocysteine conventionally represented by 1 letter code U"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:170
-name: Delta:H(-1)N(-1)18O(1)
-def: "Glycosylated asparagine 18O labeling." [PMID:1443554, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=170]
-comment: Conversion of glycosylated asparagine residues upon deglycosylation with PGNase F in 18O labelled water.
-xref: record_id "170"
-xref: delta_mono_mass "2.988261"
-xref: delta_avge_mass "2.9845"
-xref: delta_composition "H(-1) N(-1) 18O"
-xref: username_of_poster "lobvi"
-xref: group_of_poster "users"
-xref: date_time_posted "2003-12-11 18:24:58"
-xref: date_time_modified "2021-05-18 09:38:20"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:171
-name: NBS:13C(6)
-def: "Shimadzu NBS-13C." [PMID:12845591, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=171]
-synonym: "NBS reagent heavy" RELATED []
-xref: record_id "171"
-xref: delta_mono_mass "159.008578"
-xref: delta_avge_mass "159.1144"
-xref: delta_composition "H(3) 13C(6) N O(2) S"
-xref: username_of_poster "kuyama"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-01-07 07:22:34"
-xref: date_time_modified "2007-08-31 10:35:22"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:172
-name: NBS
-def: "Shimadzu NBS-12C." [PMID:12845591, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=172]
-synonym: "2-nitrobenzenesulfenyl" RELATED []
-xref: record_id "172"
-xref: delta_mono_mass "152.988449"
-xref: delta_avge_mass "153.1585"
-xref: delta_composition "H(3) C(6) N O(2) S"
-xref: username_of_poster "kuyama"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-01-07 07:25:07"
-xref: date_time_modified "2007-08-31 10:34:53"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:176
-name: BHT
-def: "Michael addition of BHT quinone methide to Cysteine and Lysine." [PMID:9448752, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=176]
-comment: BHT metabolism has been studied in rats and mice in relation to tumor promotion.
-synonym: "Butylated Hydroxytoluene" RELATED []
-xref: record_id "176"
-xref: delta_mono_mass "218.167065"
-xref: delta_avge_mass "218.3346"
-xref: delta_composition "H(22) C(15) O"
-xref: username_of_poster "gonzo"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-02-05 22:02:53"
-xref: date_time_modified "2006-10-16 15:19:41"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_1_misc_notes "Secondary adduct - much less common as C"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Other"
-xref: spec_2_misc_notes "Secondary adduct - much less common as C"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "C"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Other"
-xref: spec_3_misc_notes "Primary adduct formed"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:178
-name: DAET
-def: "Phosphorylation to amine thiol." [PMID:12216740, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=178]
-comment: DAET = 2-(dimethylamino)ethanethiol; The phosphorylation to amine is the beta elimination of phosphate and Michael addition of 2-(dimethylamino)ethanethiol to the site.
-synonym: "b-elimination thiol derivatization" RELATED []
-xref: record_id "178"
-xref: delta_mono_mass "87.050655"
-xref: delta_avge_mass "87.1866"
-xref: delta_composition "H(9) C(4) N O(-1) S"
-xref: username_of_poster "chemgirl18"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-02-11 20:34:16"
-xref: date_time_modified "2006-10-16 12:34:48"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:184
-name: Label:13C(9)
-def: "13C(9) Silac label." [URL:http\://www.pil.sdu.dk/silac_intro.htm, PMID:12716131, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=184]
-synonym: "heavy tyrosine" RELATED []
-xref: record_id "184"
-xref: delta_mono_mass "9.030193"
-xref: delta_avge_mass "8.9339"
-xref: delta_composition "C(-9) 13C(9)"
-xref: username_of_poster "hs"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-02-16 21:19:47"
-xref: date_time_modified "2007-08-22 18:31:52"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "Used in SILAC experiment"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "F"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:185
-name: Label:13C(9)+Phospho
-def: "C13 label (Phosphotyrosine)." [PMID:12716131, URL:http\://www.pil.sdu.dk/silac_intro.htm, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=185]
-synonym: "heavy phosphotyrosine" RELATED []
-xref: record_id "185"
-xref: delta_mono_mass "88.996524"
-xref: delta_avge_mass "88.9138"
-xref: delta_composition "H C(-9) 13C(9) O(3) P"
-xref: username_of_poster "hs"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-02-22 04:42:33"
-xref: date_time_modified "2006-10-16 12:37:51"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "Used in SILAC experiment"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:186
-name: HPG
-def: "Hydroxyphenylglyoxal arginine." [PMID:11698400, PMID:11914093, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=186]
-synonym: "HPG arginine" RELATED []
-xref: record_id "186"
-xref: delta_mono_mass "132.021129"
-xref: delta_avge_mass "132.1162"
-xref: delta_composition "H(4) C(8) O(2)"
-xref: username_of_poster "gcarven"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-02-26 20:19:25"
-xref: date_time_modified "2006-10-17 11:46:39"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:187
-name: 2HPG
-def: "Bis(hydroxphenylglyoxal) arginine." [PMID:11698400, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=187]
-comment: OH-PGO and PGO react with arginine at a stoichiometry of 2:1.
-xref: record_id "187"
-xref: delta_mono_mass "282.052824"
-xref: delta_avge_mass "282.2476"
-xref: delta_composition "H(10) C(16) O(5)"
-xref: username_of_poster "gcarven"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-02-26 22:05:25"
-xref: date_time_modified "2009-06-26 17:37:17"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:188
-name: Label:13C(6)
-def: "13C(6) Silac label." [URL:http\://www.pil.sdu.dk/silac_intro.htm, PMID:12716131, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=188]
-xref: record_id "188"
-xref: delta_mono_mass "6.020129"
-xref: delta_avge_mass "5.9559"
-xref: delta_composition "C(-6) 13C(6)"
-xref: username_of_poster "hs"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-02-28 19:54:10"
-xref: date_time_modified "2007-08-22 18:29:56"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "Used in SILAC experiment"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-xref: spec_2_misc_notes "Used in SILAC experiment"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "L"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Used in SILAC experiment"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "I"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Isotopic label"
-xref: spec_5_misc_notes "Used in SILAC experiment"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:193
-name: Label:18O(2)
-def: "O18 label at both C-terminal oxygens." [PMID:11467524, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=193]
-synonym: "Double O18 (C-term)" RELATED []
-xref: record_id "193"
-xref: delta_mono_mass "4.008491"
-xref: delta_avge_mass "3.9995"
-xref: delta_composition "O(-2) 18O(2)"
-xref: username_of_poster "Hensbergen"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-03-30 14:20:29"
-xref: date_time_modified "2006-11-14 12:01:04"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Any C-term"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:194
-name: AccQTag
-def: "6-aminoquinolyl-N-hydroxysuccinimidyl carbamate." [URL:http\://www2.waters.com/watprod.nsf/newdocs/930494, PMID:14997490, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=194]
-xref: record_id "194"
-xref: delta_mono_mass "170.048013"
-xref: delta_avge_mass "170.1674"
-xref: delta_composition "H(6) C(10) N(2) O"
-xref: username_of_poster "davidcreasy"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-04-08 12:01:19"
-xref: date_time_modified "2006-10-16 14:59:12"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:195
-name: QAT
-def: "APTA-d0." [PMID:15283597, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=195]
-synonym: "(3-acrylamidopropyl)trimethylammonium" RELATED []
-xref: record_id "195"
-xref: delta_mono_mass "171.149738"
-xref: delta_avge_mass "171.26"
-xref: delta_composition "H(19) C(9) N(2) O"
-xref: username_of_poster "s_julka"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-04-08 17:12:14"
-xref: date_time_modified "2009-06-26 17:39:29"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:196
-name: QAT:2H(3)
-def: "APTA d3." [PMID:15283597, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=196]
-synonym: "(3-acrylamidopropyl)trimethylammonium" RELATED []
-xref: record_id "196"
-xref: delta_mono_mass "174.168569"
-xref: delta_avge_mass "174.2784"
-xref: delta_composition "H(16) 2H(3) C(9) N(2) O"
-xref: username_of_poster "s_julka"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-04-08 17:15:04"
-xref: date_time_modified "2006-10-16 15:01:35"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:197
-name: EQAT
-def: "EAPTA d0." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=197]
-xref: record_id "197"
-xref: delta_mono_mass "184.157563"
-xref: delta_avge_mass "184.2786"
-xref: delta_composition "H(20) C(10) N(2) O"
-xref: username_of_poster "s_julka"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-04-08 17:21:08"
-xref: date_time_modified "2006-10-16 15:05:02"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:198
-name: EQAT:2H(5)
-def: "EAPTA d5." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=198]
-xref: record_id "198"
-xref: delta_mono_mass "189.188947"
-xref: delta_avge_mass "189.3094"
-xref: delta_composition "H(15) 2H(5) C(10) N(2) O"
-xref: username_of_poster "s_julka"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-04-08 17:25:24"
-xref: date_time_modified "2006-10-16 15:07:31"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:199
-name: Dimethyl:2H(4)
-def: "DiMethyl-CHD2." [PMID:14670044, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=199]
-synonym: "reductive amination" RELATED []
-xref: record_id "199"
-xref: delta_mono_mass "32.056407"
-xref: delta_avge_mass "32.0778"
-xref: delta_composition "2H(4) C(2)"
-xref: username_of_poster "PhilipHsu"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-04-20 07:07:29"
-xref: date_time_modified "2014-11-16 07:35:30"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "When dimethyl labelling is pre-digest"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "R"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:200
-name: Ethanedithiol
-def: "EDT." [PMID:11507762, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=200]
-xref: record_id "200"
-xref: delta_mono_mass "75.980527"
-xref: delta_avge_mass "76.1838"
-xref: delta_composition "H(4) C(2) O(-1) S(2)"
-xref: username_of_poster "take"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-04-20 08:27:30"
-xref: date_time_modified "2006-10-16 11:07:38"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:205
-name: Delta:H(6)C(6)O(1)
-def: "Acrolein addition +94." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=205]
-synonym: "Acrolein94, FDP" RELATED []
-xref: record_id "205"
-xref: delta_mono_mass "94.041865"
-xref: delta_avge_mass "94.1112"
-xref: delta_composition "H(6) C(6) O"
-xref: username_of_poster "fatcat"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-05-06 18:54:17"
-xref: date_time_modified "2006-10-16 12:38:28"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:206
-name: Delta:H(4)C(3)O(1)
-def: "Acrolein addition +56." [PMID:15541752, PMID:10825247, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=206]
-synonym: "Acrolein56" RELATED []
-xref: record_id "206"
-xref: delta_mono_mass "56.026215"
-xref: delta_avge_mass "56.0633"
-xref: delta_composition "H(4) C(3) O"
-xref: username_of_poster "fatcat"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-05-06 18:55:58"
-xref: date_time_modified "2017-11-08 16:29:48"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Other"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Other"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "R"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:207
-name: Delta:H(2)C(3)
-def: "Acrolein addition +38." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=207]
-synonym: "Acrolein38" RELATED []
-xref: record_id "207"
-xref: delta_mono_mass "38.01565"
-xref: delta_avge_mass "38.048"
-xref: delta_composition "H(2) C(3)"
-xref: username_of_poster "fatcat"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-05-06 18:57:08"
-xref: date_time_modified "2006-10-15 18:30:31"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:208
-name: Delta:H(4)C(6)
-def: "Acrolein addition +76." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=208]
-synonym: "Acrolein76" RELATED []
-xref: record_id "208"
-xref: delta_mono_mass "76.0313"
-xref: delta_avge_mass "76.096"
-xref: delta_composition "H(4) C(6)"
-xref: username_of_poster "fatcat"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-05-06 18:59:23"
-xref: date_time_modified "2006-10-16 11:08:13"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:209
-name: Delta:H(8)C(6)O(2)
-def: "Acrolein addition +112." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=209]
-synonym: "Acrolein112" RELATED []
-xref: record_id "209"
-xref: delta_mono_mass "112.05243"
-xref: delta_avge_mass "112.1265"
-xref: delta_composition "H(8) C(6) O(2)"
-xref: username_of_poster "fatcat"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-05-06 19:00:25"
-xref: date_time_modified "2006-10-16 12:46:03"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:211
-name: NEIAA
-def: "N-ethyl iodoacetamide-d0." [PMID:12766232, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=211]
-xref: record_id "211"
-xref: delta_mono_mass "85.052764"
-xref: delta_avge_mass "85.1045"
-xref: delta_composition "H(7) C(4) N O"
-xref: username_of_poster "Botting"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-05-18 11:10:37"
-xref: date_time_modified "2006-10-16 12:15:11"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "Y"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:212
-name: NEIAA:2H(5)
-def: "N-ethyl iodoacetamide-d5." [PMID:12766232, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=212]
-xref: record_id "212"
-xref: delta_mono_mass "90.084148"
-xref: delta_avge_mass "90.1353"
-xref: delta_composition "H(2) 2H(5) C(4) N O"
-xref: username_of_poster "Botting"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-05-18 11:11:52"
-xref: date_time_modified "2006-10-16 12:38:09"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "Y"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:213
-name: ADP-Ribosyl
-def: "ADP Ribose addition." [URL:http\://betelgeuse.u-strasbg.fr/DocPARP/DocPARG/images/Structure-pADPR.jpg, PMID:15842200, RESID:AA0231, RESID:AA0237, RESID:AA0295, FindMod:ADP, RESID:AA0168, RESID:AA0169, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=213]
-xref: record_id "213"
-xref: delta_mono_mass "541.06111"
-xref: delta_avge_mass "541.3005"
-xref: delta_composition "H(13) C(10) N(5) O(9) P(2) Pent"
-xref: username_of_poster "ionjockey"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-05-27 20:53:37"
-xref: date_time_modified "2024-08-12 09:51:41"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other glycosylation"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Other glycosylation"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "N-linked glycosylation"
-xref: spec_3_neutral_loss_0_mono_mass "0"
-xref: spec_3_neutral_loss_0_avge_mass "0"
-xref: spec_3_neutral_loss_0_flag "false"
-xref: spec_3_neutral_loss_0_composition "0"
-xref: spec_3_neutral_loss_542_mono_mass "541.06111"
-xref: spec_3_neutral_loss_542_avge_mass "541.3005"
-xref: spec_3_neutral_loss_542_flag "false"
-xref: spec_3_neutral_loss_542_composition "H(13) C(10) N(5) O(9) P(2) Pent"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "T"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "O-linked glycosylation"
-xref: spec_4_neutral_loss_542_mono_mass "541.06111"
-xref: spec_4_neutral_loss_542_avge_mass "541.3005"
-xref: spec_4_neutral_loss_542_flag "false"
-xref: spec_4_neutral_loss_542_composition "H(13) C(10) N(5) O(9) P(2) Pent"
-xref: spec_4_neutral_loss_0_mono_mass "0"
-xref: spec_4_neutral_loss_0_avge_mass "0"
-xref: spec_4_neutral_loss_0_flag "false"
-xref: spec_4_neutral_loss_0_composition "0"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "S"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "O-linked glycosylation"
-xref: spec_4_neutral_loss_0_mono_mass "0"
-xref: spec_4_neutral_loss_0_avge_mass "0"
-xref: spec_4_neutral_loss_0_flag "false"
-xref: spec_4_neutral_loss_0_composition "0"
-xref: spec_4_neutral_loss_542_mono_mass "541.06111"
-xref: spec_4_neutral_loss_542_avge_mass "541.3005"
-xref: spec_4_neutral_loss_542_flag "false"
-xref: spec_4_neutral_loss_542_composition "H(13) C(10) N(5) O(9) P(2) Pent"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "E"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Other glycosylation"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "K"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Other glycosylation"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "D"
-xref: spec_7_position "Anywhere"
-xref: spec_7_classification "Other glycosylation"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:214
-name: iTRAQ4plex
-def: "Representative mass and accurate mass for 116 & 117." [URL:http\://docs.appliedbiosystems.com/pebiodocs/04351918.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=214]
-comment: Different channels have the same nominal mass but slightly different exact masses. Use this value for all channels for quantitation purposes. mTRAQ heavy is identical to iTRAQ4plex 117.
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry AKA iTRAQ4plex116/7" RELATED []
-xref: record_id "214"
-xref: delta_mono_mass "144.102063"
-xref: delta_avge_mass "144.1544"
-xref: delta_composition "H(12) C(4) 13C(3) N 15N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2004-06-08 14:04:07"
-xref: date_time_modified "2024-08-12 09:52:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "0"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Low abundance"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "H"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "Very low abundance"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "S"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Isotopic label"
-xref: spec_5_misc_notes "Very low abundance"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "T"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Isotopic label"
-xref: spec_6_misc_notes "Very low abundance"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "N-term"
-xref: spec_7_position "Protein N-term"
-xref: spec_7_classification "Isotopic label"
-xref: spec_8_group "8"
-xref: spec_8_hidden "1"
-xref: spec_8_site "C"
-xref: spec_8_position "Anywhere"
-xref: spec_8_classification "Isotopic label"
-xref: spec_8_misc_notes "side reaction"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:243
-name: IGBP
-def: "Light IDBEST tag for quantitation." [URL:http\://www.targetdiscovery.com/index.php?topic=prod.idbe, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=243]
-xref: record_id "243"
-xref: delta_mono_mass "296.016039"
-xref: delta_avge_mass "297.1478"
-xref: delta_composition "H(13) C(12) N(2) O(2) Br"
-xref: username_of_poster "zqiao"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-07-26 23:02:04"
-xref: date_time_modified "2006-10-19 11:13:26"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:253
-name: Crotonaldehyde
-def: "Crotonaldehyde." [PMID:11283024, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=253]
-xref: record_id "253"
-xref: delta_mono_mass "70.041865"
-xref: delta_avge_mass "70.0898"
-xref: delta_composition "H(6) C(4) O"
-xref: username_of_poster "fatcat"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-08-12 19:56:03"
-xref: date_time_modified "2006-10-16 10:35:31"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Other"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:254
-name: Delta:H(2)C(2)
-def: "Acetaldehyde +26." [PMID:7744761, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=254]
-comment: Lys modification is formation of Schiff base.
-xref: record_id "254"
-xref: delta_mono_mass "26.01565"
-xref: delta_avge_mass "26.0373"
-xref: delta_composition "H(2) C(2)"
-xref: username_of_poster "fatcat"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-08-12 20:01:03"
-xref: date_time_modified "2011-11-21 13:14:17"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Other"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Other"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "N-term"
-xref: spec_4_position "Any N-term"
-xref: spec_4_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:255
-name: Delta:H(4)C(2)
-def: "Acetaldehyde +28." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=255]
-comment: Reduction of Schiff base formed between K amino group and acetaldehyde.
-xref: record_id "255"
-xref: delta_mono_mass "28.0313"
-xref: delta_avge_mass "28.0532"
-xref: delta_composition "H(4) C(2)"
-xref: username_of_poster "fatcat"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-08-12 20:02:38"
-xref: date_time_modified "2011-11-21 13:14:58"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Other"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:256
-name: Delta:H(4)C(3)
-def: "Propionaldehyde +40." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=256]
-xref: record_id "256"
-xref: delta_mono_mass "40.0313"
-xref: delta_avge_mass "40.0639"
-xref: delta_composition "H(4) C(3)"
-xref: username_of_poster "fatcat"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-08-12 20:04:01"
-xref: date_time_modified "2010-02-25 10:49:55"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Other"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:258
-name: Label:18O(1)
-def: "O18 Labeling." [PMID:11467524, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=258]
-synonym: "H2 18O Alkaline Phosphatase" RELATED []
-xref: record_id "258"
-xref: delta_mono_mass "2.004246"
-xref: delta_avge_mass "1.9998"
-xref: delta_composition "O(-1) 18O"
-xref: username_of_poster "chemgirl18"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-08-27 21:57:17"
-xref: date_time_modified "2006-10-13 18:53:41"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "alkaline phosphatase to dephosphorylate"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-xref: spec_2_misc_notes "alkaline phosphatase to dephosphorylate"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "alkaline phosphatase to dephosphorylate"
-xref: spec_4_group "4"
-xref: spec_4_hidden "0"
-xref: spec_4_site "C-term"
-xref: spec_4_position "Any C-term"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "digesting in labelled water"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:259
-name: Label:13C(6)15N(2)
-def: "13C(6) 15N(2) Silac label." [PMID:12716131, URL:http\://www.pil.sdu.dk/silac_intro.htm, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=259]
-synonym: "heavy lysine" RELATED []
-xref: record_id "259"
-xref: delta_mono_mass "8.014199"
-xref: delta_avge_mass "7.9427"
-xref: delta_composition "C(-6) 13C(6) N(-2) 15N(2)"
-xref: username_of_poster "hs01"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-08-30 16:23:02"
-xref: date_time_modified "2014-06-09 09:40:49"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "Used in SILAC experiment"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:260
-name: Thiophospho
-def: "Thiophosphorylation." [PMID:12110917, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=260]
-xref: record_id "260"
-xref: delta_mono_mass "95.943487"
-xref: delta_avge_mass "96.0455"
-xref: delta_composition "H O(2) P S"
-xref: username_of_poster "mrbladergroen"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-09-01 13:20:58"
-xref: date_time_modified "2006-10-16 12:38:48"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Other"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:261
-name: SPITC
-def: "4-sulfophenyl isothiocyanate." [URL:http\://www.shimadzu-biotech.net/literature/application_note/202_1.pdf, PMID:14745769, PMID:14689565, PMID:16526082, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=261]
-synonym: "N-terminal / lysine sulfonation" RELATED []
-xref: record_id "261"
-xref: delta_mono_mass "214.971084"
-xref: delta_avge_mass "215.2495"
-xref: delta_composition "H(5) C(7) N O(3) S(2)"
-xref: username_of_poster "hatlevig"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-09-14 20:01:29"
-xref: date_time_modified "2006-10-16 15:26:00"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:262
-name: Label:2H(3)
-def: "Trideuteration." [URL:http\://www.pil.sdu.dk/silac_intro.htm, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=262]
-synonym: "Trideuteration" RELATED []
-xref: record_id "262"
-xref: delta_mono_mass "3.01883"
-xref: delta_avge_mass "3.0185"
-xref: delta_composition "H(-3) 2H(3)"
-xref: username_of_poster "mmolloy"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-09-29 08:52:01"
-xref: date_time_modified "2013-02-22 12:42:11"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "for SILAC expt"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "M"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:264
-name: PET
-def: "Phosphorylation to pyridyl thiol." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=264]
-comment: PET = 2-[4-pyridyl]ethanethiol. This modification is a chemical derivative, based on a alkaline catalysed beta-elimination of phosphoserines and phosphothreonines and subsequent 1,4-addition of 2-[4-pyridine]ethanethiol. These modified serines and threonines produce in MS/MS a characteristic fragment which can be used for precursor-ion-scan experiments.
-synonym: "b-elimination PET derivatisation" RELATED []
-xref: record_id "264"
-xref: delta_mono_mass "121.035005"
-xref: delta_avge_mass "121.2028"
-xref: delta_composition "H(7) C(7) N O(-1) S"
-xref: username_of_poster "vbad"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-10-07 08:55:33"
-xref: date_time_modified "2006-10-16 12:48:51"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:267
-name: Label:13C(6)15N(4)
-def: "13C(6) 15N(4) Silac label." [URL:http\://www.pil.sdu.dk/silac_intro.htm, PMID:12716131, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=267]
-xref: record_id "267"
-xref: delta_mono_mass "10.008269"
-xref: delta_avge_mass "9.9296"
-xref: delta_composition "C(-6) 13C(6) N(-4) 15N(4)"
-xref: username_of_poster "AFCS"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-10-20 17:49:33"
-xref: date_time_modified "2006-10-19 10:30:51"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "Used in SILAC experiment"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:268
-name: Label:13C(5)15N(1)
-def: "13C(5) 15N(1) Silac label." [PMID:12771378, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=268]
-xref: record_id "268"
-xref: delta_mono_mass "6.013809"
-xref: delta_avge_mass "5.9567"
-xref: delta_composition "C(-5) 13C(5) N(-1) 15N"
-xref: username_of_poster "Deepa"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-11-05 18:49:37"
-xref: date_time_modified "2011-11-21 14:48:39"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "Used in AQUA experiment"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "P"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-xref: spec_2_misc_notes "Result of conversion of 13C6, 15N4 arginine to 13C5, 15N1 proline"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "M"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "SILAC label used in COFRADIC"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "E"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:269
-name: Label:13C(9)15N(1)
-def: "13C(9) 15N(1) Silac label." [URL:http\://www.pil.sdu.dk/silac_intro.htm, PMID:12771378, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=269]
-xref: record_id "269"
-xref: delta_mono_mass "10.027228"
-xref: delta_avge_mass "9.9273"
-xref: delta_composition "C(-9) 13C(9) N(-1) 15N"
-xref: username_of_poster "Deepa"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-11-05 18:51:13"
-xref: date_time_modified "2006-10-19 10:31:10"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "Used in AQUA experiment"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:270
-name: Cytopiloyne
-def: "Nucleophilic addtion to cytopiloyne." [PMID:15549660, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=270]
-comment: Cytopiloyne is a polyacetylenic glucoside isolated form Bidens pilosa which can modulate T helper cell differentiation. Biotinylated cytopiloyne might be use to identify its receptor in T cell.
-xref: record_id "270"
-xref: delta_mono_mass "362.136553"
-xref: delta_avge_mass "362.3738"
-xref: delta_composition "H(22) C(19) O(7)"
-xref: username_of_poster "ymchiang"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-11-10 03:13:23"
-xref: date_time_modified "2006-10-16 16:35:54"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "P"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "R"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "S"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "Y"
-xref: spec_7_position "Anywhere"
-xref: spec_7_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:271
-name: Cytopiloyne+water
-def: "Nucleophilic addition to cytopiloyne+H2O." [PMID:15549660, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=271]
-comment: Cytopiloyne is a polyacetylenic glucoside isolated form Bidens pilosa which can modulated T helper cell differentiation. Biotinylated cytopiloyne might be use to identify its receptor in T cell.
-xref: record_id "271"
-xref: delta_mono_mass "380.147118"
-xref: delta_avge_mass "380.3891"
-xref: delta_composition "H(24) C(19) O(8)"
-xref: username_of_poster "ymchiang"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-11-11 05:23:17"
-xref: date_time_modified "2006-10-16 16:37:10"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "R"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "S"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "T"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "Y"
-xref: spec_7_position "Anywhere"
-xref: spec_7_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:272
-name: CAF
-def: "Sulfonation of N-terminus." [PMID:15732931, PMID:16046801, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=272]
-comment: N-terminal sulfonation of diglycine to detect ubiquitination sites.
-synonym: "Ettan CAF MALDI" RELATED []
-xref: record_id "272"
-xref: delta_mono_mass "135.983029"
-xref: delta_avge_mass "136.1265"
-xref: delta_composition "H(4) C(3) O(4) S"
-xref: username_of_poster "chens002"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-11-16 14:25:33"
-xref: date_time_modified "2007-01-03 19:34:35"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:275
-name: Nitrosyl
-def: "Nitrosylation." [FindMod:NTRY, PMID:10442087, RESID:AA0230, PMID:15688001, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=275]
-xref: record_id "275"
-xref: delta_mono_mass "28.990164"
-xref: delta_avge_mass "28.9982"
-xref: delta_composition "H(-1) N O"
-xref: username_of_poster "dengh"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-12-11 00:23:12"
-xref: date_time_modified "2019-09-10 09:17:23"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_1_misc_notes "S-nitrosylation"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "Y"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_2_misc_notes "photochemical decomposition"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:276
-name: AEBS
-def: "Aminoethylbenzenesulfonylation." [PMID:8597590, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=276]
-comment: Potential protein modification when using AEBSF (Pefabloc) as a serine protease inhibitor.
-xref: record_id "276"
-xref: delta_mono_mass "183.035399"
-xref: delta_avge_mass "183.2276"
-xref: delta_composition "H(9) C(8) N O(2) S"
-xref: username_of_poster "plattm"
-xref: group_of_poster "users"
-xref: date_time_posted "2004-12-14 04:38:25"
-xref: date_time_modified "2006-10-16 15:04:42"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Artefact"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "S"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Artefact"
-xref: spec_4_misc_notes "Primary site of modification"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "Y"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:278
-name: Ethanolyl
-def: "Ethanolation." [PMID:15351294, PMID:7730303, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=278]
-synonym: "Hydroxy ethyl" RELATED []
-xref: record_id "278"
-xref: delta_mono_mass "44.026215"
-xref: delta_avge_mass "44.0526"
-xref: delta_composition "H(4) C(2) O"
-xref: username_of_poster "knierman"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-01-11 04:26:47"
-xref: date_time_modified "2017-10-09 15:47:39"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "from reaction of SH group with iodoethanol"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_2_misc_notes "reduced form of oxidation product"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "R"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_misc_notes "reduced form of oxidation product"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:280
-name: Ethyl
-def: "Ethylation." [PMID:9629898, URL:http\://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2911956&tool=pmcentrez&rendertype=abstract, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=280]
-xref: record_id "280"
-xref: delta_mono_mass "28.0313"
-xref: delta_avge_mass "28.0532"
-xref: delta_composition "H(4) C(2)"
-xref: username_of_poster "Qishanl"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-01-27 23:18:07"
-xref: date_time_modified "2015-08-26 14:42:10"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Multiple"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Multiple"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "E"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Artefact"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "N-term"
-xref: spec_4_position "Protein N-term"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "C-term"
-xref: spec_5_position "Any C-term"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "D"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:281
-name: CoenzymeA
-def: "Cysteine modified Coenzyme A." [URL:http\://commons.wikimedia.org/wiki/Image\:Coenzyme_a.png, RESID:AA0306, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=281]
-xref: record_id "281"
-xref: delta_mono_mass "765.09956"
-xref: delta_avge_mass "765.5182"
-xref: delta_composition "H(34) C(21) N(7) O(16) P(3) S"
-xref: username_of_poster "tremis"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-02-01 17:10:00"
-xref: date_time_modified "2006-10-16 17:15:18"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:284
-name: Methyl:2H(2)
-def: "Deuterium Methylation of Lysine." [PMID:15525938, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=284]
-xref: record_id "284"
-xref: delta_mono_mass "16.028204"
-xref: delta_avge_mass "16.0389"
-xref: delta_composition "2H(2) C"
-xref: username_of_poster "Glebivanov"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-02-13 01:26:38"
-xref: date_time_modified "2016-06-14 11:53:24"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:285
-name: SulfanilicAcid
-def: "Light Sulfanilic Acid (SA) C12." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=285]
-synonym: "C-Terminal/Glutamate/Aspartate sulfonation" RELATED []
-xref: record_id "285"
-xref: delta_mono_mass "155.004099"
-xref: delta_avge_mass "155.1744"
-xref: delta_composition "H(5) C(6) N O(2) S"
-xref: username_of_poster "apanchaud"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-02-17 15:48:07"
-xref: date_time_modified "2006-10-16 14:05:34"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Any C-term"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "D"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "E"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:286
-name: SulfanilicAcid:13C(6)
-def: "Heavy Sulfanilic Acid (SA) C13." [PMID:9254591, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=286]
-synonym: "C-Terminal/Glutamate/Aspartate sulfonation" RELATED []
-xref: record_id "286"
-xref: delta_mono_mass "161.024228"
-xref: delta_avge_mass "161.1303"
-xref: delta_composition "H(5) 13C(6) N O(2) S"
-xref: username_of_poster "apanchaud"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-02-17 15:55:52"
-xref: date_time_modified "2006-10-16 14:08:42"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Any C-term"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "D"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "E"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:288
-name: Trp->Oxolactone
-def: "Tryptophan oxidation to oxolactone." [PMID:7949339, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=288]
-comment: The cleavage of a peptide bond between Try-Xxx with oxidation of tryptophan to the oxolactone occurs in the presence of BNPS-skatole. This is a useful method for the chemical cleavage of proteins specifically at tryptophan residues.
-xref: record_id "288"
-xref: delta_mono_mass "13.979265"
-xref: delta_avge_mass "13.9835"
-xref: delta_composition "H(-2) O"
-xref: username_of_poster "oxolactone"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-02-25 23:30:20"
-xref: date_time_modified "2006-10-14 10:06:01"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:289
-name: Biotin-PEO-Amine
-def: "Biotin polyethyleneoxide amine." [URL:http\://www.piercenet.com/Proteomics/browse.cfm?fldID=84EBE112-F871-4CA5-807F-47327153CFCB, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=289]
-comment: EDC crosslinker is used to couple biotin PEO-amine to carboxyl groups or 5\' phosphate groups.
-xref: record_id "289"
-xref: delta_mono_mass "356.188212"
-xref: delta_avge_mass "356.4835"
-xref: delta_composition "H(28) C(16) N(4) O(3) S"
-xref: username_of_poster "TBricker1"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-03-02 16:49:17"
-xref: date_time_modified "2006-11-14 11:15:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Protein C-term"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "EDC-coupled modification of D, E and C-terminus"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "D"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_2_misc_notes "EDC-coupled modification of D, E and C-terminus"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "E"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_misc_notes "EDC-coupled modification of D, E and C-terminus"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:290
-name: Biotin-HPDP
-def: "Pierce EZ-Link Biotin-HPDP." [URL:http\://www.piercenet.com/Products/Browse.cfm?fldID=01031002, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=290]
-xref: record_id "290"
-xref: delta_mono_mass "428.191582"
-xref: delta_avge_mass "428.6124"
-xref: delta_composition "H(32) C(19) N(4) O(3) S(2)"
-xref: username_of_poster "tgreco"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-03-03 22:56:52"
-xref: date_time_modified "2010-12-03 16:28:07"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:291
-name: Delta:Hg(1)
-def: "Mercury Mercaptan." [PMID:10695144, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=291]
-xref: record_id "291"
-xref: delta_mono_mass "201.970617"
-xref: delta_avge_mass "200.59"
-xref: delta_composition "Hg"
-xref: username_of_poster "tgreco"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-03-03 23:53:00"
-xref: date_time_modified "2006-10-16 15:09:18"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:292
-name: IodoU-AMP
-def: "(Iodo)-uracil MP." [PMID:11567090, PMID:11112526, PMID:6540775, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=292]
-comment: One note about this chemistry is that for W you have to take care of O2 big time (and extract the I-uracil monophosphate with organics to get rid of residual iodide).
-synonym: "UV induced linkage of Iodo-U-amp with WFY" RELATED []
-xref: record_id "292"
-xref: delta_mono_mass "322.020217"
-xref: delta_avge_mass "322.1654"
-xref: delta_composition "H(11) C(9) N(2) O(9) P"
-xref: username_of_poster "davidERICanderson"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-03-04 22:57:55"
-xref: date_time_modified "2017-01-31 13:36:23"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "Used in base/residue interactions (in principle?)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "W"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_2_misc_notes "Used in base/residue interactions (observed)"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_misc_notes "Used in base/residue interactions (in principle?)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:293
-name: CAMthiopropanoyl
-def: "3-(carbamidomethylthio)propanoyl." [PMID:15121203, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=293]
-synonym: "3-thiopropanoyl moiety from reduced DSP crosslinker or NHS-SS-biotin, modified with Iodoacetamide" RELATED []
-xref: record_id "293"
-xref: delta_mono_mass "145.019749"
-xref: delta_avge_mass "145.1796"
-xref: delta_composition "H(7) C(5) N O(2) S"
-xref: username_of_poster "vanschra"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-03-09 15:22:46"
-xref: date_time_modified "2006-10-16 13:58:55"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:294
-name: IED-Biotin
-def: "Biotinoyl-iodoacetyl-ethylenediamine." [PMID:10906242, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=294]
-xref: record_id "294"
-xref: delta_mono_mass "326.141261"
-xref: delta_avge_mass "326.4145"
-xref: delta_composition "H(22) C(14) N(4) O(3) S"
-xref: username_of_poster "alexey"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-03-10 16:28:09"
-xref: date_time_modified "2006-10-16 15:53:29"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:295
-name: dHex
-def: "Fucose." [PMID:15189151, PMID:11344537, URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=295]
-synonym: "deoxyhexose" RELATED []
-xref: record_id "295"
-xref: delta_mono_mass "146.057909"
-xref: delta_avge_mass "146.1412"
-xref: delta_composition "dHex"
-xref: username_of_poster "rsack"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-03-22 16:57:00"
-xref: date_time_modified "2017-11-23 11:42:26"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_147_mono_mass "146.057909"
-xref: spec_1_neutral_loss_147_avge_mass "146.1412"
-xref: spec_1_neutral_loss_147_flag "false"
-xref: spec_1_neutral_loss_147_composition "dHex"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_147_mono_mass "146.057909"
-xref: spec_1_neutral_loss_147_avge_mass "146.1412"
-xref: spec_1_neutral_loss_147_flag "false"
-xref: spec_1_neutral_loss_147_composition "dHex"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_misc_notes "Not reported for human proteins"
-xref: spec_2_neutral_loss_147_mono_mass "146.057909"
-xref: spec_2_neutral_loss_147_avge_mass "146.1412"
-xref: spec_2_neutral_loss_147_flag "false"
-xref: spec_2_neutral_loss_147_composition "dHex"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:298
-name: Methyl:2H(3)
-def: "Deuterated methyl ester." [URL:http\://www.sigmaaldrich.com/technical-documents/articles/stable-isotopes/stable-isotope-labeling-by-amino-acids.html, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=298]
-xref: record_id "298"
-xref: delta_mono_mass "17.03448"
-xref: delta_avge_mass "17.0451"
-xref: delta_composition "H(-1) 2H(3) C"
-xref: username_of_poster "ndacoyas"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-03-24 16:31:28"
-xref: date_time_modified "2013-02-07 16:43:18"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "esterification of carboxylic acids using D3-Methanolic HCl"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "D"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-xref: spec_2_misc_notes "esterification of carboxylic acids using D3-Methanolic HCl"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "E"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "esterification of carboxylic acids using D3-Methanolic HCl"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "K"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "SILAC labelling with L-Methionine-(methyl-d3)"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "R"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Isotopic label"
-xref: spec_5_misc_notes "SILAC labelling with L-Methionine-(methyl-d3)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:299
-name: Carboxy
-def: "Carboxylation." [RESID:AA0114, FindMod:GGLU, RESID:AA0363, RESID:AA0032, PMID:3802193, RESID:AA0304, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=299]
-xref: record_id "299"
-xref: delta_mono_mass "43.989829"
-xref: delta_avge_mass "44.0095"
-xref: delta_composition "C O(2)"
-xref: username_of_poster "Carol"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-03-29 22:55:44"
-xref: date_time_modified "2006-11-14 11:08:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "D"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-xref: spec_3_misc_notes "Gamma-carboxylation"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "E"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Post-translational"
-xref: spec_4_misc_notes "Gamma-carboxylation"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "M"
-xref: spec_5_position "Protein N-term"
-xref: spec_5_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:301
-name: Bromobimane
-def: "Monobromobimane derivative." [PMID:7856876, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=301]
-synonym: "mBromobimane" RELATED []
-xref: record_id "301"
-xref: delta_mono_mass "190.074228"
-xref: delta_avge_mass "190.1986"
-xref: delta_composition "H(10) C(10) N(2) O(2)"
-xref: username_of_poster "catsriku"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-04-04 23:03:13"
-xref: date_time_modified "2006-10-16 15:07:49"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:302
-name: Menadione
-def: "Menadione quinone derivative." [PMID:15939799, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=302]
-synonym: "Vitamin k3 (Q)" RELATED []
-xref: record_id "302"
-xref: delta_mono_mass "170.036779"
-xref: delta_avge_mass "170.1641"
-xref: delta_composition "H(6) C(11) O(2)"
-xref: username_of_poster "catsriku"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-04-04 23:21:29"
-xref: date_time_modified "2007-07-12 07:36:32"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:303
-name: DeStreak
-def: "Cysteine mercaptoethanol." [PMID:12442261, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=303]
-xref: record_id "303"
-xref: delta_mono_mass "75.998285"
-xref: delta_avge_mass "76.1176"
-xref: delta_composition "H(4) C(2) O S"
-xref: username_of_poster "harald"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-04-11 14:06:08"
-xref: date_time_modified "2006-10-16 11:07:55"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:305
-name: dHex(1)Hex(3)HexNAc(4)
-def: "FA2/G0F." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=305]
-xref: record_id "305"
-xref: delta_mono_mass "1444.53387"
-xref: delta_avge_mass "1445.3331"
-xref: delta_composition "dHex Hex(3) HexNAc(4)"
-xref: username_of_poster "whaskins"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-04-25 18:20:12"
-xref: date_time_modified "2020-08-02 11:42:31"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1445_mono_mass "1444.53387"
-xref: spec_1_neutral_loss_1445_avge_mass "1445.3331"
-xref: spec_1_neutral_loss_1445_flag "false"
-xref: spec_1_neutral_loss_1445_composition "dHex Hex(3) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_1445_mono_mass "1444.53387"
-xref: spec_2_neutral_loss_1445_avge_mass "1445.3331"
-xref: spec_2_neutral_loss_1445_flag "false"
-xref: spec_2_neutral_loss_1445_composition "dHex Hex(3) HexNAc(4)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_1445_mono_mass "1444.53387"
-xref: spec_2_neutral_loss_1445_avge_mass "1445.3331"
-xref: spec_2_neutral_loss_1445_flag "false"
-xref: spec_2_neutral_loss_1445_composition "dHex Hex(3) HexNAc(4)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:307
-name: dHex(1)Hex(4)HexNAc(4)
-def: "FA2G1/G1F." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=4&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=307]
-synonym: "dHex Hex(4) HexNAc(4) ---OR--- Hex(4) HexNAc(4) Pent Me" RELATED []
-xref: record_id "307"
-xref: delta_mono_mass "1606.586693"
-xref: delta_avge_mass "1607.4737"
-xref: delta_composition "dHex Hex(4) HexNAc(4)"
-xref: username_of_poster "whaskins"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-04-25 19:22:11"
-xref: date_time_modified "2020-08-02 11:55:46"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1607_mono_mass "1606.586693"
-xref: spec_1_neutral_loss_1607_avge_mass "1607.4737"
-xref: spec_1_neutral_loss_1607_flag "false"
-xref: spec_1_neutral_loss_1607_composition "dHex Hex(4) HexNAc(4)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_1607_mono_mass "1606.586693"
-xref: spec_2_neutral_loss_1607_avge_mass "1607.4737"
-xref: spec_2_neutral_loss_1607_flag "false"
-xref: spec_2_neutral_loss_1607_composition "dHex Hex(4) HexNAc(4)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_1607_mono_mass "1606.586693"
-xref: spec_2_neutral_loss_1607_avge_mass "1607.4737"
-xref: spec_2_neutral_loss_1607_flag "false"
-xref: spec_2_neutral_loss_1607_composition "dHex Hex(4) HexNAc(4)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:308
-name: dHex(1)Hex(5)HexNAc(4)
-def: "FA2G2/G2F." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=5&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=308]
-xref: record_id "308"
-xref: delta_mono_mass "1768.639517"
-xref: delta_avge_mass "1769.6143"
-xref: delta_composition "dHex Hex(5) HexNAc(4)"
-xref: username_of_poster "whaskins"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-04-25 19:25:17"
-xref: date_time_modified "2020-08-02 11:41:19"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1769_mono_mass "1768.639517"
-xref: spec_1_neutral_loss_1769_avge_mass "1769.6143"
-xref: spec_1_neutral_loss_1769_flag "false"
-xref: spec_1_neutral_loss_1769_composition "dHex Hex(5) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:309
-name: Hex(3)HexNAc(4)
-def: "A2/G0." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=309]
-xref: record_id "309"
-xref: delta_mono_mass "1298.475961"
-xref: delta_avge_mass "1299.1919"
-xref: delta_composition "Hex(3) HexNAc(4)"
-xref: username_of_poster "whaskins"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-04-25 19:27:51"
-xref: date_time_modified "2020-08-02 11:39:23"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1299_mono_mass "1298.475961"
-xref: spec_1_neutral_loss_1299_avge_mass "1299.1919"
-xref: spec_1_neutral_loss_1299_flag "false"
-xref: spec_1_neutral_loss_1299_composition "Hex(3) HexNAc(4)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_1299_mono_mass "1298.475961"
-xref: spec_2_neutral_loss_1299_avge_mass "1299.1919"
-xref: spec_2_neutral_loss_1299_flag "false"
-xref: spec_2_neutral_loss_1299_composition "Hex(3) HexNAc(4)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_1299_mono_mass "1298.475961"
-xref: spec_2_neutral_loss_1299_avge_mass "1299.1919"
-xref: spec_2_neutral_loss_1299_flag "false"
-xref: spec_2_neutral_loss_1299_composition "Hex(3) HexNAc(4)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:310
-name: Hex(4)HexNAc(4)
-def: "A2G1/G1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=310]
-xref: record_id "310"
-xref: delta_mono_mass "1460.528784"
-xref: delta_avge_mass "1461.3325"
-xref: delta_composition "Hex(4) HexNAc(4)"
-xref: username_of_poster "whaskins"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-04-25 19:33:37"
-xref: date_time_modified "2020-08-02 11:38:53"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1461_mono_mass "1460.528784"
-xref: spec_1_neutral_loss_1461_avge_mass "1461.3325"
-xref: spec_1_neutral_loss_1461_flag "false"
-xref: spec_1_neutral_loss_1461_composition "Hex(4) HexNAc(4)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_1461_mono_mass "1460.528784"
-xref: spec_2_neutral_loss_1461_avge_mass "1461.3325"
-xref: spec_2_neutral_loss_1461_flag "false"
-xref: spec_2_neutral_loss_1461_composition "Hex(4) HexNAc(4)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_1461_mono_mass "1460.528784"
-xref: spec_2_neutral_loss_1461_avge_mass "1461.3325"
-xref: spec_2_neutral_loss_1461_flag "false"
-xref: spec_2_neutral_loss_1461_composition "Hex(4) HexNAc(4)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:311
-name: Hex(5)HexNAc(4)
-def: "A2G2/G2." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=5&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=311]
-xref: record_id "311"
-xref: delta_mono_mass "1622.581608"
-xref: delta_avge_mass "1623.4731"
-xref: delta_composition "Hex(5) HexNAc(4)"
-xref: username_of_poster "whaskins"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-04-25 19:35:54"
-xref: date_time_modified "2020-08-02 11:38:17"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1623_mono_mass "1622.581608"
-xref: spec_1_neutral_loss_1623_avge_mass "1623.4731"
-xref: spec_1_neutral_loss_1623_flag "false"
-xref: spec_1_neutral_loss_1623_composition "Hex(5) HexNAc(4)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_misc_notes "Not reported for human proteins"
-xref: spec_2_neutral_loss_1623_mono_mass "1622.581608"
-xref: spec_2_neutral_loss_1623_avge_mass "1623.4731"
-xref: spec_2_neutral_loss_1623_flag "false"
-xref: spec_2_neutral_loss_1623_composition "Hex(5) HexNAc(4)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_misc_notes "Not reported for human proteins"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_1623_mono_mass "1622.581608"
-xref: spec_2_neutral_loss_1623_avge_mass "1623.4731"
-xref: spec_2_neutral_loss_1623_flag "false"
-xref: spec_2_neutral_loss_1623_composition "Hex(5) HexNAc(4)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:312
-name: Cysteinyl
-def: "Cysteinylation." [RESID:AA0025, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=312]
-xref: record_id "312"
-xref: delta_mono_mass "119.004099"
-xref: delta_avge_mass "119.1423"
-xref: delta_composition "H(5) C(3) N O(2) S"
-xref: username_of_poster "whaskins"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-04-25 19:59:43"
-xref: date_time_modified "2006-12-17 11:28:36"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Multiple"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:313
-name: Lys-loss
-def: "Loss of Lysine." [PMID:16078144, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=313]
-xref: record_id "313"
-xref: delta_mono_mass "-128.094963"
-xref: delta_avge_mass "-128.1723"
-xref: delta_composition "H(-12) C(-6) N(-2) O(-1)"
-xref: username_of_poster "whaskins"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-04-25 20:05:38"
-xref: date_time_modified "2021-09-06 11:24:44"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Protein C-term"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Artefact"
-xref: spec_2_misc_notes "Error in peptide synthesis"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:314
-name: Nmethylmaleimide
-def: "Nmethylmaleimide." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=314]
-xref: record_id "314"
-xref: delta_mono_mass "111.032028"
-xref: delta_avge_mass "111.0987"
-xref: delta_composition "H(5) C(5) N O(2)"
-xref: username_of_poster "whaskins"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-04-25 20:12:24"
-xref: date_time_modified "2006-10-16 17:26:09"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:316
-name: DimethylpyrroleAdduct
-def: "2,5-dimethypyrrole." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=316]
-xref: record_id "316"
-xref: delta_mono_mass "78.04695"
-xref: delta_avge_mass "78.1118"
-xref: delta_composition "H(6) C(6)"
-xref: username_of_poster "Qishanl"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-05-07 03:11:23"
-xref: date_time_modified "2006-10-16 11:14:22"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:318
-name: Delta:H(2)C(5)
-def: "MDA adduct +62." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=318]
-comment: Usually major adduct formed from malondialdehyde (MDA) with the amino group of lysine residues.
-synonym: "MDA62" RELATED []
-xref: record_id "318"
-xref: delta_mono_mass "62.01565"
-xref: delta_avge_mass "62.0694"
-xref: delta_composition "H(2) C(5)"
-xref: username_of_poster "rkupfer"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-05-12 22:00:21"
-xref: date_time_modified "2006-10-16 10:29:55"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:319
-name: Delta:H(2)C(3)O(1)
-def: "MDA adduct +54." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=319]
-synonym: "MDA54" RELATED []
-xref: record_id "319"
-xref: delta_mono_mass "54.010565"
-xref: delta_avge_mass "54.0474"
-xref: delta_composition "H(2) C(3) O"
-xref: username_of_poster "rkupfer"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-05-12 22:12:10"
-xref: date_time_modified "2006-10-16 10:15:34"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "Malondialdehyde (MDA) adduct"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "R"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_2_misc_notes "5-hydro-5-methylimidazol-4-one, Methylglyoxal adduct"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:320
-name: Nethylmaleimide+water
-def: "Nethylmaleimidehydrolysis." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=320]
-xref: record_id "320"
-xref: delta_mono_mass "143.058243"
-xref: delta_avge_mass "143.1406"
-xref: delta_composition "H(9) C(6) N O(3)"
-xref: username_of_poster "whaskins"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-05-16 22:18:42"
-xref: date_time_modified "2006-10-17 11:40:14"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:323
-name: Xlink:B10621
-def: "Bis-((N-iodoacetyl)piperazinyl)sulfonerhodamine." [URL:https\://www.thermofisher.com/us/en/home/references/molecular-probes-the-handbook/crosslinking-and-photoactivatable-reagents/chemical-crosslinking-reagents.html#head2, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=323]
-comment: Discontinued Invitrogen X-link reagent.
-synonym: "BSR monolink" RELATED []
-xref: record_id "323"
-xref: delta_mono_mass "713.093079"
-xref: delta_avge_mass "713.5626"
-xref: delta_composition "H(30) C(31) N(4) O(6) S I"
-xref: username_of_poster "dengh"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-05-17 22:56:12"
-xref: date_time_modified "2017-09-05 15:32:46"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:324
-name: Xlink:DTBP[87]
-def: "Cleaved and reduced DTBP crosslinker." [PMID:770170, URL:http\://tools.thermofisher.com/content/sfs/manuals/MAN0011314_ImidoesterCrsLnk_DMA_DMP_DMS_DTBP_UG.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=324]
-comment: Imidoester cross-linker.
-synonym: "dimethyl 3,3'-dithiobispropionimidate" RELATED []
-xref: record_id "324"
-xref: delta_mono_mass "87.01427"
-xref: delta_avge_mass "87.1435"
-xref: delta_composition "H(5) C(3) N S"
-xref: username_of_poster "takesin"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-05-18 08:43:26"
-xref: date_time_modified "2017-08-18 14:19:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:325
-name: FP-Biotin
-def: "10-ethoxyphosphinyl-N-(biotinamidopentyl)decanamide." [PMID:10611275, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=325]
-comment: FP-biotin was designed to label the active site serine of serine esterases/proteases.
-synonym: "O-ethyl-N-(biotinamidopentyl)decanamido phosphonate" RELATED []
-xref: record_id "325"
-xref: delta_mono_mass "572.316129"
-xref: delta_avge_mass "572.7405"
-xref: delta_composition "H(49) C(27) N(4) O(5) P S"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-05-19 22:01:37"
-xref: date_time_modified "2010-02-24 20:54:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "Y"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "K"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:327
-name: Delta:H(4)C(2)O(-1)S(1)
-def: "S-Ethylcystine from Serine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=327]
-comment: Phosphoserine to S-ethylcystine via Beta elimination/Michael addition of ethylthiol.
-xref: record_id "327"
-xref: delta_mono_mass "44.008456"
-xref: delta_avge_mass "44.1188"
-xref: delta_composition "H(4) C(2) O(-1) S"
-xref: username_of_poster "UCDMSF"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-06-20 20:09:02"
-xref: date_time_modified "2006-10-16 10:00:57"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:329
-name: Methyl:2H(3)13C(1)
-def: "Monomethylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=329]
-xref: record_id "329"
-xref: delta_mono_mass "18.037835"
-xref: delta_avge_mass "18.0377"
-xref: delta_composition "H(-1) 2H(3) 13C"
-xref: username_of_poster "sams"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-06-30 18:19:34"
-xref: date_time_modified "2016-06-14 11:54:23"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:330
-name: Dimethyl:2H(6)13C(2)
-def: "Dimethylation." [PMID:15782174, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=330]
-xref: record_id "330"
-xref: delta_mono_mass "36.07567"
-xref: delta_avge_mass "36.0754"
-xref: delta_composition "H(-2) 2H(6) 13C(2)"
-xref: username_of_poster "sams"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-06-30 18:21:32"
-xref: date_time_modified "2014-11-16 07:36:47"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Isotopic label"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "N-term"
-xref: spec_4_position "Protein N-term"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "When dimethyl labelling is pre-digest"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:332
-name: Thiophos-S-S-biotin
-def: "Thiophosphate labeled with biotin-HPDP." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=332]
-synonym: "Thiophos-biotin disulfide" RELATED []
-xref: record_id "332"
-xref: delta_mono_mass "525.142894"
-xref: delta_avge_mass "525.6658"
-xref: delta_composition "H(34) C(19) N(4) O(5) P S(3)"
-xref: username_of_poster "lparker"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-07-21 16:37:10"
-xref: date_time_modified "2006-10-16 17:02:42"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_neutral_loss_526_mono_mass "525.142894"
-xref: spec_1_neutral_loss_526_avge_mass "525.6658"
-xref: spec_1_neutral_loss_526_flag "false"
-xref: spec_1_neutral_loss_526_composition "H(34) C(19) N(4) O(5) P S(3)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_2_neutral_loss_526_mono_mass "525.142894"
-xref: spec_2_neutral_loss_526_avge_mass "525.6658"
-xref: spec_2_neutral_loss_526_flag "false"
-xref: spec_2_neutral_loss_526_composition "H(34) C(19) N(4) O(5) P S(3)"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_neutral_loss_526_mono_mass "525.142894"
-xref: spec_3_neutral_loss_526_avge_mass "525.6658"
-xref: spec_3_neutral_loss_526_flag "false"
-xref: spec_3_neutral_loss_526_composition "H(34) C(19) N(4) O(5) P S(3)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:333
-name: Can-FP-biotin
-def: "6-N-biotinylaminohexyl isopropyl phosphate." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=333]
-comment: Commercially available from Toronto Research Chemicals Inc, as of 2005. Designed to label the active site serine of serine esterases/proteases.
-synonym: "O-isopropyl-N-biotinylaminohexyl phosphonate" RELATED []
-xref: record_id "333"
-xref: delta_mono_mass "447.195679"
-xref: delta_avge_mass "447.5291"
-xref: delta_composition "H(34) C(19) N(3) O(5) P S"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-07-21 20:54:00"
-xref: date_time_modified "2010-12-03 16:24:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "Y"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:335
-name: HNE+Delta:H(2)
-def: "Reduced 4-Hydroxynonenal." [PMID:11910026, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=335]
-comment: Michael addition adduct of 4-hydroxynonenal with histidine, cystein and lysine residues stabilized by reduction with NaBH4.
-xref: record_id "335"
-xref: delta_mono_mass "158.13068"
-xref: delta_avge_mass "158.238"
-xref: delta_composition "H(18) C(9) O(2)"
-xref: username_of_poster "rkupfer"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-08-10 20:52:36"
-xref: date_time_modified "2011-07-18 11:28:34"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:337
-name: Methylamine
-def: "Michael addition with methylamine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=337]
-xref: record_id "337"
-xref: delta_mono_mass "13.031634"
-xref: delta_avge_mass "13.0418"
-xref: delta_composition "H(3) C N O(-1)"
-xref: username_of_poster "zhulx"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-08-12 21:55:51"
-xref: date_time_modified "2006-10-14 10:02:51"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:340
-name: Bromo
-def: "Bromination." [PMID:9033387, RESID:AA0174, RESID:AA0175, RESID:AA0176, RESID:AA0173, RESID:AA0180, RESID:AA0179, FindMod:BROM, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=340]
-xref: record_id "340"
-xref: delta_mono_mass "77.910511"
-xref: delta_avge_mass "78.8961"
-xref: delta_composition "H(-1) Br"
-xref: username_of_poster "gerribe"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-09-06 08:31:51"
-xref: date_time_modified "2011-11-21 12:07:51"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "F"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "Y"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:342
-name: Amino
-def: "Tyrosine oxidation to 2-aminotyrosine." [PMID:9252331, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=342]
-xref: record_id "342"
-xref: delta_mono_mass "15.010899"
-xref: delta_avge_mass "15.0146"
-xref: delta_composition "H N"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-09-10 21:18:23"
-xref: date_time_modified "2006-10-14 10:39:53"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:343
-name: Argbiotinhydrazide
-def: "Oxidized Arginine biotinylated with biotin hydrazide." [PMID:15828771, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=343]
-xref: record_id "343"
-xref: delta_mono_mass "199.066699"
-xref: delta_avge_mass "199.27"
-xref: delta_composition "H(13) C(9) N O(2) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-09-10 22:36:58"
-xref: date_time_modified "2006-11-14 12:10:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:344
-name: Arg->GluSA
-def: "Arginine oxidation to glutamic semialdehyde." [PMID:9252331, PMID:1680314, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=344]
-synonym: "Arginine oxidation to gamma-glutamyl semialdehyde" RELATED []
-xref: record_id "344"
-xref: delta_mono_mass "-43.053433"
-xref: delta_avge_mass "-43.0711"
-xref: delta_composition "H(-5) C(-1) N(-3) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-09-10 22:38:24"
-xref: date_time_modified "2006-11-16 15:25:28"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:345
-name: Trioxidation
-def: "Cysteine oxidation to cysteic acid." [PMID:14678012, PMID:9252331, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=345]
-xref: record_id "345"
-xref: delta_mono_mass "47.984744"
-xref: delta_avge_mass "47.9982"
-xref: delta_composition "O(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-09-10 22:39:38"
-xref: date_time_modified "2017-11-08 16:28:19"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "W"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "F"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:348
-name: His->Asn
-def: "His->Asn substitution." [PMID:9252331, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=348]
-synonym: "histidine oxidation to aspargine" RELATED []
-xref: record_id "348"
-xref: delta_mono_mass "-23.015984"
-xref: delta_avge_mass "-23.0366"
-xref: delta_composition "H(-1) C(-2) N(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-09-10 22:43:27"
-xref: date_time_modified "2011-06-23 12:00:22"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_1_misc_notes "Could also be classed as chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:349
-name: His->Asp
-def: "His->Asp substitution." [PMID:9252331, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=349]
-synonym: "histidine oxidation to aspartic acid" RELATED []
-xref: record_id "349"
-xref: delta_mono_mass "-22.031969"
-xref: delta_avge_mass "-22.0519"
-xref: delta_composition "H(-2) C(-2) N(-2) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-09-10 22:44:32"
-xref: date_time_modified "2011-06-23 12:00:45"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_1_misc_notes "Could also be classed as chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:350
-name: Trp->Hydroxykynurenin
-def: "Tryptophan oxidation to hydroxykynurenin." [URL:http\://www.lbqp.unb.br/bioq/htm/aulas2D/deg_aa_ile_leu_trp.htm?reload_coolmenus, PMID:9252331, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=350]
-xref: record_id "350"
-xref: delta_mono_mass "19.989829"
-xref: delta_avge_mass "19.9881"
-xref: delta_composition "C(-1) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-09-10 22:47:20"
-xref: date_time_modified "2006-11-14 17:40:45"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:351
-name: Trp->Kynurenin
-def: "Tryptophan oxidation to kynurenin." [PMID:9252331, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=351]
-xref: record_id "351"
-xref: delta_mono_mass "3.994915"
-xref: delta_avge_mass "3.9887"
-xref: delta_composition "C(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-09-10 22:48:33"
-xref: date_time_modified "2006-10-14 09:39:53"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:352
-name: Lys->Allysine
-def: "Lysine oxidation to aminoadipic semialdehyde." [RESID:AA0121, FindMod:ALLYS, PMID:9252331, PMID:11120890, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=352]
-xref: record_id "352"
-xref: delta_mono_mass "-1.031634"
-xref: delta_avge_mass "-1.0311"
-xref: delta_composition "H(-3) N(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-09-10 22:49:59"
-xref: date_time_modified "2006-10-13 18:27:28"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:353
-name: Lysbiotinhydrazide
-def: "Oxidized Lysine biotinylated with biotin hydrazide." [URL:http\://www.piercenet.com/Proteomics/browse.cfm?fldID=84EBE112-F871-4CA5-807F-47327153CFCB, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=353]
-xref: record_id "353"
-xref: delta_mono_mass "241.088497"
-xref: delta_avge_mass "241.31"
-xref: delta_composition "H(15) C(10) N(3) O(2) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-09-10 22:51:13"
-xref: date_time_modified "2006-11-14 12:12:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:354
-name: Nitro
-def: "Oxidation to nitro." [PMID:8839040, PMID:9252331, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=354]
-xref: record_id "354"
-xref: delta_mono_mass "44.985078"
-xref: delta_avge_mass "44.9976"
-xref: delta_composition "H(-1) N O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-09-10 22:52:38"
-xref: date_time_modified "2017-11-08 16:26:39"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "Y"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "F"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:357
-name: probiotinhydrazide
-def: "Oxidized proline biotinylated with biotin hydrazide." [URL:http\://www.piercenet.com/Proteomics/browse.cfm?fldID=84EBE112-F871-4CA5-807F-47327153CFCB, PMID:15174056, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=357]
-xref: record_id "357"
-xref: delta_mono_mass "258.115047"
-xref: delta_avge_mass "258.3405"
-xref: delta_composition "H(18) C(10) N(4) O(2) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-09-10 22:56:20"
-xref: date_time_modified "2006-11-14 12:12:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:359
-name: Pro->pyro-Glu
-def: "Proline oxidation to pyroglutamic acid." [PMID:9252331, PMID:10717661, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=359]
-xref: record_id "359"
-xref: delta_mono_mass "13.979265"
-xref: delta_avge_mass "13.9835"
-xref: delta_composition "H(-2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-09-10 22:58:42"
-xref: date_time_modified "2006-10-14 10:03:34"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:360
-name: Pro->Pyrrolidinone
-def: "Proline oxidation to pyrrolidinone." [PMID:9252331, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=360]
-xref: record_id "360"
-xref: delta_mono_mass "-30.010565"
-xref: delta_avge_mass "-30.026"
-xref: delta_composition "H(-2) C(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-09-10 23:00:19"
-xref: date_time_modified "2006-10-13 15:37:42"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:361
-name: Thrbiotinhydrazide
-def: "Oxidized Threonine biotinylated with biotin hydrazide." [URL:http\://www.piercenet.com/Proteomics/browse.cfm?fldID=84EBE112-F871-4CA5-807F-47327153CFCB, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=361]
-xref: record_id "361"
-xref: delta_mono_mass "240.104482"
-xref: delta_avge_mass "240.3252"
-xref: delta_composition "H(16) C(10) N(4) O S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-09-10 23:01:28"
-xref: date_time_modified "2006-11-14 12:12:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:362
-name: Diisopropylphosphate
-def: "O-Diisopropylphosphorylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=362]
-comment: A selective label for the active site serine of the serine esterase/protease family. It has also been shown to label tyrosine in serum albumin.
-xref: record_id "362"
-xref: delta_mono_mass "164.060231"
-xref: delta_avge_mass "164.1394"
-xref: delta_composition "H(13) C(6) O(3) P"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-09-14 18:05:04"
-xref: date_time_modified "2011-12-05 16:14:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "K"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "N-term"
-xref: spec_5_position "Any N-term"
-xref: spec_5_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:363
-name: Isopropylphospho
-def: "O-Isopropylphosphorylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=363]
-comment: Created by auto-catalytic dealkylation of the O-Diisopropylphosphate adduct.
-xref: record_id "363"
-xref: delta_mono_mass "122.013281"
-xref: delta_avge_mass "122.0596"
-xref: delta_composition "H(7) C(3) O(3) P"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-09-14 18:08:20"
-xref: date_time_modified "2007-01-15 15:25:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:364
-name: ICPL:13C(6)
-def: "Bruker Daltonics SERVA-ICPL(TM) quantification chemistry, heavy form." [URL:http\://www.bdal.de/life-science-tools/care-consumables-more/icpl-kit.html, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=364]
-comment: Attention: As the digest is typically applied AFTER ICPL_light/heavy labeling, only ProteinN-term labeling and Lys-specific labeling is applied.
-xref: record_id "364"
-xref: delta_mono_mass "111.041593"
-xref: delta_avge_mass "111.05"
-xref: delta_composition "H(3) 13C(6) N O"
-xref: username_of_poster "suckau"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-09-19 12:45:52"
-xref: date_time_modified "2008-09-03 15:27:07"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_2_misc_notes "Use when labelling pre-digest"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Use when labelling post-digest"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:365
-name: ICPL
-def: "Bruker Daltonics SERVA-ICPL(TM) quantification chemistry, light form." [URL:http\://www.bdal.de/life-science-tools/care-consumables-more/icpl-kit.html, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=365]
-comment: Attention: As the digest is typically applied AFTER ICPL_light/heavy labeling, only ProteinN-term labeling and Lys-specific labeling is applied.
-xref: record_id "365"
-xref: delta_mono_mass "105.021464"
-xref: delta_avge_mass "105.0941"
-xref: delta_composition "H(3) C(6) N O"
-xref: username_of_poster "suckau"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-09-19 13:00:14"
-xref: date_time_modified "2008-09-03 15:26:36"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_2_misc_notes "Use when labelling pre-digest"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Use when labelling post-digest"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:366
-name: Deamidated:18O(1)
-def: "Deamidation in presence of O18." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=366]
-comment: Observed.
-xref: record_id "366"
-xref: delta_mono_mass "2.988261"
-xref: delta_avge_mass "2.9845"
-xref: delta_composition "H(-1) N(-1) 18O"
-xref: username_of_poster "gerribe"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-09-22 15:30:16"
-xref: date_time_modified "2006-10-14 09:35:33"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:368
-name: Cys->Dha
-def: "Dehydroalanine (from Cysteine)." [PMID:11212008, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=368]
-xref: record_id "368"
-xref: delta_mono_mass "-33.987721"
-xref: delta_avge_mass "-34.0809"
-xref: delta_composition "H(-2) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-02 17:31:11"
-xref: date_time_modified "2006-10-13 15:27:46"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:369
-name: Pro->Pyrrolidone
-def: "Pyrrolidone from Proline." [PMID:9252331, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=369]
-xref: record_id "369"
-xref: delta_mono_mass "-27.994915"
-xref: delta_avge_mass "-28.0101"
-xref: delta_composition "C(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-02 17:39:05"
-xref: date_time_modified "2006-11-14 11:12:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:371
-name: HMVK
-def: "Michael addition of hydroxymethylvinyl ketone to cysteine." [PMID:11743741, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=371]
-synonym: "hydroxymethylvinyl ketone" RELATED []
-xref: record_id "371"
-xref: delta_mono_mass "86.036779"
-xref: delta_avge_mass "86.0892"
-xref: delta_composition "H(6) C(4) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-03 15:59:33"
-xref: date_time_modified "2006-10-16 12:15:35"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:372
-name: Arg->Orn
-def: "Ornithine from Arginine." [PMID:15489230, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=372]
-xref: record_id "372"
-xref: delta_mono_mass "-42.021798"
-xref: delta_avge_mass "-42.04"
-xref: delta_composition "H(-2) C(-1) N(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-05 17:55:25"
-xref: date_time_modified "2006-10-13 15:26:33"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:374
-name: Dehydro
-def: "Half of a disulfide bridge." [RESID:AA0025, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=374]
-xref: record_id "374"
-xref: delta_mono_mass "-1.007825"
-xref: delta_avge_mass "-1.0079"
-xref: delta_composition "H(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-06 20:57:01"
-xref: date_time_modified "2006-10-13 18:28:17"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Multiple"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:375
-name: Diphthamide
-def: "Diphthamide." [RESID:AA0040, FindMod:DIPH, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=375]
-xref: record_id "375"
-xref: delta_mono_mass "142.110613"
-xref: delta_avge_mass "142.1989"
-xref: delta_composition "H(14) C(7) N(2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-06 23:21:29"
-xref: date_time_modified "2015-09-08 17:15:11"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:376
-name: Hydroxyfarnesyl
-def: "Hydroxyfarnesyl." [RESID:AA0103, FindMod:FAR0, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=376]
-xref: record_id "376"
-xref: delta_mono_mass "220.182715"
-xref: delta_avge_mass "220.3505"
-xref: delta_composition "H(24) C(15) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-07 20:36:20"
-xref: date_time_modified "2006-10-16 15:20:11"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:377
-name: Diacylglycerol
-def: "Diacylglycerol." [RESID:AA0107, FindMod:DIAC, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=377]
-xref: record_id "377"
-xref: delta_mono_mass "576.511761"
-xref: delta_avge_mass "576.9334"
-xref: delta_composition "H(68) C(37) O(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-07 20:41:21"
-xref: date_time_modified "2006-10-16 17:05:40"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:378
-name: Carboxyethyl
-def: "Carboxyethyl." [RESID:AA0115, FindMod:CETH, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=378]
-synonym: "Ethoxyformylation" RELATED []
-xref: record_id "378"
-xref: delta_mono_mass "72.021129"
-xref: delta_avge_mass "72.0627"
-xref: delta_composition "H(4) C(3) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-07 22:18:20"
-xref: date_time_modified "2024-08-12 10:05:50"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_2_misc_notes "Labeling with diethylpyrocarbonate (DEPC)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:379
-name: Hypusine
-def: "Hypusine." [RESID:AA0116, FindMod:HYPU, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=379]
-xref: record_id "379"
-xref: delta_mono_mass "87.068414"
-xref: delta_avge_mass "87.1204"
-xref: delta_composition "H(9) C(4) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-07 22:20:53"
-xref: date_time_modified "2006-10-16 12:35:24"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:380
-name: Retinylidene
-def: "Retinal." [RESID:AA0120, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=380]
-xref: record_id "380"
-xref: delta_mono_mass "266.203451"
-xref: delta_avge_mass "266.4204"
-xref: delta_composition "H(26) C(20)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-07 22:27:27"
-xref: date_time_modified "2006-10-16 15:47:14"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:381
-name: Lys->AminoadipicAcid
-def: "Alpha-amino adipic acid." [RESID:AA0122, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=381]
-xref: record_id "381"
-xref: delta_mono_mass "14.96328"
-xref: delta_avge_mass "14.9683"
-xref: delta_composition "H(-3) N(-1) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 17:41:37"
-xref: date_time_modified "2006-10-14 10:33:11"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:382
-name: Cys->PyruvicAcid
-def: "Pyruvic acid from N-term cys." [RESID:AA0127, FindMod:PYRUC, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=382]
-xref: record_id "382"
-xref: delta_mono_mass "-33.003705"
-xref: delta_avge_mass "-33.0961"
-xref: delta_composition "H(-3) N(-1) O S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 17:48:42"
-xref: date_time_modified "2006-10-13 16:42:55"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Protein N-term"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:385
-name: Ammonia-loss
-def: "Loss of ammonia." [RESID:AA0127, FindMod:PYRUS, RESID:AA0129, FindMod:OXOB, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=385]
-synonym: "oxobutanoic acid from N term Thr pyruvic acid from N-term ser" RELATED []
-xref: record_id "385"
-xref: delta_mono_mass "-17.026549"
-xref: delta_avge_mass "-17.0305"
-xref: delta_composition "H(-3) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 18:00:01"
-xref: date_time_modified "2007-07-15 20:11:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Protein N-term"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "0"
-xref: spec_3_site "C"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Artefact"
-xref: spec_3_misc_notes "Pyro-carbamidomethyl as a delta from Carbamidomethyl-Cys"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "N"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_4_misc_notes "N-Succinimide"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:387
-name: Phycocyanobilin
-def: "Phycocyanobilin." [RESID:AA0258, RESID:AA0131, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=387]
-comment: Phycocyanobilin and phycobiliviolin have different structures but the same empirical formula.
-synonym: "phycobiliviolin" RELATED []
-xref: record_id "387"
-xref: delta_mono_mass "586.279135"
-xref: delta_avge_mass "586.678"
-xref: delta_composition "H(38) C(33) N(4) O(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 18:06:19"
-xref: date_time_modified "2006-10-16 17:07:44"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:388
-name: Phycoerythrobilin
-def: "Phycoerythrobilin." [RESID:AA0132, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=388]
-xref: record_id "388"
-xref: delta_mono_mass "588.294785"
-xref: delta_avge_mass "588.6939"
-xref: delta_composition "H(40) C(33) N(4) O(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 18:08:38"
-xref: date_time_modified "2006-10-16 17:08:02"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:389
-name: Phytochromobilin
-def: "Phytochromobilin." [RESID:AA0133, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=389]
-xref: record_id "389"
-xref: delta_mono_mass "584.263485"
-xref: delta_avge_mass "584.6621"
-xref: delta_composition "H(36) C(33) N(4) O(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 18:23:58"
-xref: date_time_modified "2006-10-16 17:07:22"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:390
-name: Heme
-def: "Heme." [RESID:AA0329, RESID:AA0135, RESID:AA0276, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=390]
-xref: record_id "390"
-xref: delta_mono_mass "616.177295"
-xref: delta_avge_mass "616.4873"
-xref: delta_composition "H(32) C(34) N(4) O(4) Fe"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 18:27:20"
-xref: date_time_modified "2006-10-16 17:10:28"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:391
-name: Molybdopterin
-def: "Molybdopterin." [RESID:AA0142, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=391]
-xref: record_id "391"
-xref: delta_mono_mass "521.884073"
-xref: delta_avge_mass "520.2668"
-xref: delta_composition "H(11) C(10) N(5) O(8) P S(2) Mo"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 18:46:19"
-xref: date_time_modified "2006-10-16 17:02:25"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:392
-name: Quinone
-def: "Quinone." [RESID:AA0147, RESID:AA0148, FindMod:TOPA, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=392]
-xref: record_id "392"
-xref: delta_mono_mass "29.974179"
-xref: delta_avge_mass "29.9829"
-xref: delta_composition "H(-2) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 18:56:28"
-xref: date_time_modified "2006-10-15 18:03:47"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "W"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:393
-name: Glucosylgalactosyl
-def: "Glucosylgalactosyl hydroxylysine." [RESID:AA0153, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=393]
-xref: record_id "393"
-xref: delta_mono_mass "340.100562"
-xref: delta_avge_mass "340.2806"
-xref: delta_composition "O Hex(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 19:19:13"
-xref: date_time_modified "2015-05-01 14:08:37"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other glycosylation"
-xref: spec_1_neutral_loss_341_mono_mass "340.100562"
-xref: spec_1_neutral_loss_341_avge_mass "340.2806"
-xref: spec_1_neutral_loss_341_flag "false"
-xref: spec_1_neutral_loss_341_composition "O Hex(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:394
-name: GPIanchor
-def: "Glycosylphosphatidylinositol." [RESID:AA0158, RESID:AA0159, RESID:AA0160, RESID:AA0161, RESID:AA0162, RESID:AA0163, RESID:AA0164, RESID:AA0165, RESID:AA0166, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=394]
-xref: record_id "394"
-xref: delta_mono_mass "123.00853"
-xref: delta_avge_mass "123.0477"
-xref: delta_composition "H(6) C(2) N O(3) P"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 19:31:10"
-xref: date_time_modified "2006-11-14 11:13:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Protein C-term"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:395
-name: PhosphoribosyldephosphoCoA
-def: "Phosphoribosyl dephospho-coenzyme A." [RESID:AA0167, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=395]
-xref: record_id "395"
-xref: delta_mono_mass "881.146904"
-xref: delta_avge_mass "881.6335"
-xref: delta_composition "H(42) C(26) N(7) O(19) P(3) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 19:42:56"
-xref: date_time_modified "2006-10-16 17:19:42"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:396
-name: GlycerylPE
-def: "Glycerylphosphorylethanolamine." [RESID:AA0170, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=396]
-xref: record_id "396"
-xref: delta_mono_mass "197.04531"
-xref: delta_avge_mass "197.1262"
-xref: delta_composition "H(12) C(5) N O(5) P"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 19:50:17"
-xref: date_time_modified "2006-10-16 15:08:39"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:397
-name: Triiodothyronine
-def: "Triiodo." [RESID:AA0177, FindMod:THRN, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=397]
-xref: record_id "397"
-xref: delta_mono_mass "469.716159"
-xref: delta_avge_mass "469.785"
-xref: delta_composition "H C(6) O I(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 20:08:28"
-xref: date_time_modified "2006-10-16 16:59:19"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:398
-name: Thyroxine
-def: "Tetraiodo." [RESID:AA0178, FindMod:THRX, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=398]
-xref: record_id "398"
-xref: delta_mono_mass "595.612807"
-xref: delta_avge_mass "595.6815"
-xref: delta_composition "C(6) O I(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 20:10:14"
-xref: date_time_modified "2006-10-16 17:08:51"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:400
-name: Tyr->Dha
-def: "Dehydroalanine (from Tyrosine)." [RESID:AA0181, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=400]
-xref: record_id "400"
-xref: delta_mono_mass "-94.041865"
-xref: delta_avge_mass "-94.1112"
-xref: delta_composition "H(-6) C(-6) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 20:17:48"
-xref: date_time_modified "2006-10-13 15:02:50"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:401
-name: Didehydro
-def: "2-amino-3-oxo-butanoic_acid." [RESID:AA0183, RESID:AA0185, PMID:9252331, RESID:AA0365, FindMod:OXOAS, FindMod:DHY, PMID:15705169, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=401]
-synonym: "oxoalanine" RELATED []
-xref: record_id "401"
-xref: delta_mono_mass "-2.01565"
-xref: delta_avge_mass "-2.0159"
-xref: delta_composition "H(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 20:23:58"
-xref: date_time_modified "2008-07-30 12:01:47"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_2_misc_notes "oxoalanine formylglycine"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "K"
-xref: spec_4_position "Any C-term"
-xref: spec_4_classification "Artefact"
-xref: spec_4_misc_notes "Lactone formation from C-terminal hydroxylysine"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:402
-name: Cys->Oxoalanine
-def: "Oxoalanine." [RESID:AA0185, FindMod:OXOAC, PMID:18722427, PMID:17450134, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=402]
-synonym: "formylglycine" RELATED []
-xref: record_id "402"
-xref: delta_mono_mass "-17.992806"
-xref: delta_avge_mass "-18.0815"
-xref: delta_composition "H(-2) O S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 20:29:10"
-xref: date_time_modified "2009-03-13 16:04:03"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:403
-name: Ser->LacticAcid
-def: "Lactic acid from N-term Ser." [RESID:AA0186, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=403]
-xref: record_id "403"
-xref: delta_mono_mass "-15.010899"
-xref: delta_avge_mass "-15.0146"
-xref: delta_composition "H(-1) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 20:34:16"
-xref: date_time_modified "2006-10-13 17:18:52"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Protein N-term"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:405
-name: Phosphoadenosine
-def: "AMP." [RESID:AA0267, RESID:AA0203, RESID:AA0371, RESID:AA0227, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=405]
-xref: record_id "405"
-xref: delta_mono_mass "329.05252"
-xref: delta_avge_mass "329.2059"
-xref: delta_composition "H(12) C(10) N(5) O(6) P"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 21:34:01"
-xref: date_time_modified "2024-08-12 10:05:28"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_136_mono_mass "135.054495"
-xref: spec_1_neutral_loss_136_avge_mass "135.1267"
-xref: spec_1_neutral_loss_136_flag "false"
-xref: spec_1_neutral_loss_136_composition "H(5) C(5) N(5)"
-xref: spec_1_neutral_loss_250_mono_mass "249.086189"
-xref: spec_1_neutral_loss_250_avge_mass "249.226"
-xref: spec_1_neutral_loss_250_flag "false"
-xref: spec_1_neutral_loss_250_composition "H(11) C(10) N(5) O(3)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-xref: spec_3_neutral_loss_348_mono_mass "347.063085"
-xref: spec_3_neutral_loss_348_avge_mass "347.2212"
-xref: spec_3_neutral_loss_348_flag "false"
-xref: spec_3_neutral_loss_348_composition "H(14) C(10) N(5) O(7) P"
-xref: spec_3_neutral_loss_0_mono_mass "0"
-xref: spec_3_neutral_loss_0_avge_mass "0"
-xref: spec_3_neutral_loss_0_flag "false"
-xref: spec_3_neutral_loss_0_composition "0"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "H"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Post-translational"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "S"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Post-translational"
-xref: spec_5_neutral_loss_348_mono_mass "347.063085"
-xref: spec_5_neutral_loss_348_avge_mass "347.2212"
-xref: spec_5_neutral_loss_348_flag "false"
-xref: spec_5_neutral_loss_348_composition "H(14) C(10) N(5) O(7) P"
-xref: spec_5_neutral_loss_0_mono_mass "0"
-xref: spec_5_neutral_loss_0_avge_mass "0"
-xref: spec_5_neutral_loss_0_flag "false"
-xref: spec_5_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:407
-name: Hydroxycinnamyl
-def: "Hydroxycinnamyl." [RESID:AA0207, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=407]
-xref: record_id "407"
-xref: delta_mono_mass "146.036779"
-xref: delta_avge_mass "146.1427"
-xref: delta_composition "H(6) C(9) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 21:40:43"
-xref: date_time_modified "2006-10-16 14:02:07"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:408
-name: Glycosyl
-def: "Glycosyl-L-hydroxyproline." [RESID:AA0212, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=408]
-xref: record_id "408"
-xref: delta_mono_mass "148.037173"
-xref: delta_avge_mass "148.114"
-xref: delta_composition "H(-2) C(-1) Hex"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 21:57:16"
-xref: date_time_modified "2015-05-01 13:14:26"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other glycosylation"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:409
-name: FMNH
-def: "Flavin mononucleotide." [RESID:AA0353, RESID:AA0220, RESID:AA0352, FindMod:FMNH, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=409]
-xref: record_id "409"
-xref: delta_mono_mass "454.088965"
-xref: delta_avge_mass "454.3279"
-xref: delta_composition "H(19) C(17) N(4) O(9) P"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 22:09:45"
-xref: date_time_modified "2006-10-16 16:57:46"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:410
-name: Archaeol
-def: "S-diphytanylglycerol diether." [RESID:AA0223, FindMod:ARCH, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=410]
-xref: record_id "410"
-xref: delta_mono_mass "634.662782"
-xref: delta_avge_mass "635.1417"
-xref: delta_composition "H(86) C(43) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-11 22:15:37"
-xref: date_time_modified "2006-10-16 17:10:59"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:411
-name: Phenylisocyanate
-def: "Phenyl isocyanate." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=411]
-xref: record_id "411"
-xref: delta_mono_mass "119.037114"
-xref: delta_avge_mass "119.1207"
-xref: delta_composition "H(5) C(7) N O"
-xref: username_of_poster "TING"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-10-14 21:13:16"
-xref: date_time_modified "2006-10-16 12:48:08"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:412
-name: Phenylisocyanate:2H(5)
-def: "D5-phenyl isocyanate." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=412]
-xref: record_id "412"
-xref: delta_mono_mass "124.068498"
-xref: delta_avge_mass "124.1515"
-xref: delta_composition "2H(5) C(7) N O"
-xref: username_of_poster "TING"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-10-14 21:16:11"
-xref: date_time_modified "2006-10-16 13:35:26"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:413
-name: Phosphoguanosine
-def: "Phospho-guanosine." [RESID:AA0325, RESID:AA0228, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=413]
-xref: record_id "413"
-xref: delta_mono_mass "345.047435"
-xref: delta_avge_mass "345.2053"
-xref: delta_composition "H(12) C(10) N(5) O(7) P"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 15:50:03"
-xref: date_time_modified "2006-10-16 16:01:42"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:414
-name: Hydroxymethyl
-def: "Hydroxymethyl." [RESID:AA0236, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=414]
-xref: record_id "414"
-xref: delta_mono_mass "30.010565"
-xref: delta_avge_mass "30.026"
-xref: delta_composition "H(2) C O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 16:12:56"
-xref: date_time_modified "2006-10-15 18:04:18"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:415
-name: MolybdopterinGD+Delta:S(-1)Se(1)
-def: "L-selenocysteinyl molybdenum bis(molybdopterin guanine dinucleotide)." [RESID:AA0248, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=415]
-xref: record_id "415"
-xref: delta_mono_mass "1620.930224"
-xref: delta_avge_mass "1618.9096"
-xref: delta_composition "H(47) C(40) N(20) O(26) P(4) S(3) Se Mo"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 16:27:56"
-xref: date_time_modified "2006-10-17 11:44:58"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:416
-name: Dipyrrolylmethanemethyl
-def: "Dipyrrolylmethanemethyl." [RESID:AA0252, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=416]
-xref: record_id "416"
-xref: delta_mono_mass "418.137616"
-xref: delta_avge_mass "418.3973"
-xref: delta_composition "H(22) C(20) N(2) O(8)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 16:33:24"
-xref: date_time_modified "2006-11-14 10:37:01"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:417
-name: PhosphoUridine
-def: "Uridine phosphodiester." [RESID:AA0256, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=417]
-xref: record_id "417"
-xref: delta_mono_mass "306.025302"
-xref: delta_avge_mass "306.166"
-xref: delta_composition "H(11) C(9) N(2) O(8) P"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 16:38:18"
-xref: date_time_modified "2006-10-16 15:52:11"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:419
-name: Glycerophospho
-def: "Glycerophospho." [RESID:AA0264, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=419]
-xref: record_id "419"
-xref: delta_mono_mass "154.00311"
-xref: delta_avge_mass "154.0584"
-xref: delta_composition "H(7) C(3) O(5) P"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 17:02:51"
-xref: date_time_modified "2006-10-16 14:03:40"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:420
-name: Carboxy->Thiocarboxy
-def: "Thiocarboxylic acid." [FindMod:THIOG, RESID:AA0265, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=420]
-xref: record_id "420"
-xref: delta_mono_mass "15.977156"
-xref: delta_avge_mass "16.0656"
-xref: delta_composition "O(-1) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 17:08:53"
-xref: date_time_modified "2006-10-14 10:59:20"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Protein C-term"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:421
-name: Sulfide
-def: "Persulfide." [RESID:AA0269, URL:http\://www.nestgrp.com/protocols/bmt/pi3tr.shtml, FindMod:CYSP, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=421]
-xref: record_id "421"
-xref: delta_mono_mass "31.972071"
-xref: delta_avge_mass "32.065"
-xref: delta_composition "S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 17:22:45"
-xref: date_time_modified "2012-11-23 11:25:27"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "D"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_2_misc_notes "beta-thiolation"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "W"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_misc_notes "Addition of a single sulfur atom by Pi3-Tryptophan reagent to create thiol"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:422
-name: PyruvicAcidIminyl
-def: "N-pyruvic acid 2-iminyl." [RESID:AA0287, RESID:AA0274, RESID:AA0275, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=422]
-xref: record_id "422"
-xref: delta_mono_mass "70.005479"
-xref: delta_avge_mass "70.0468"
-xref: delta_composition "H(2) C(3) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 17:30:48"
-xref: date_time_modified "2006-10-16 10:35:08"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Protein N-term"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "V"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:423
-name: Delta:Se(1)
-def: "Selenyl." [RESID:AA0277, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=423]
-xref: record_id "423"
-xref: delta_mono_mass "79.91652"
-xref: delta_avge_mass "78.96"
-xref: delta_composition "Se"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 17:49:48"
-xref: date_time_modified "2006-10-16 11:14:44"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:424
-name: MolybdopterinGD
-def: "Molybdenum bis(molybdopterin guanine dinucleotide)." [RESID:AA0375, RESID:AA0281, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=424]
-xref: record_id "424"
-xref: delta_mono_mass "1572.985775"
-xref: delta_avge_mass "1572.0146"
-xref: delta_composition "H(47) C(40) N(20) O(26) P(4) S(4) Mo"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 17:53:48"
-xref: date_time_modified "2016-02-01 14:23:12"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "D"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "U"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:425
-name: Dioxidation
-def: "Dihydroxy." [PMID:9252331, RESID:AA0282, RESID:AA0370, FindMod:DIHYDR, FindMod:MSONE, FindMod:CSIA, PMID:12686488, RESID:AA0262, RESID:AA0369, RESID:AA0263, RESID:AA0251, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=425]
-xref: record_id "425"
-xref: delta_mono_mass "31.989829"
-xref: delta_avge_mass "31.9988"
-xref: delta_composition "O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 17:59:33"
-xref: date_time_modified "2017-11-03 09:33:41"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "R"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-xref: spec_4_group "4"
-xref: spec_4_hidden "0"
-xref: spec_4_site "M"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Post-translational"
-xref: spec_4_misc_notes "Sulphone"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "F"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_5_misc_notes "phenylalanine oxidation to dihydroxyphenylalanine"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "W"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-xref: spec_6_misc_notes "tryptophan oxidation to formylkynurenin"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "Y"
-xref: spec_7_position "Anywhere"
-xref: spec_7_classification "Post-translational"
-xref: spec_7_misc_notes "trihydroxyphenylalanine"
-xref: spec_8_group "8"
-xref: spec_8_hidden "1"
-xref: spec_8_site "C"
-xref: spec_8_position "Anywhere"
-xref: spec_8_classification "Post-translational"
-xref: spec_8_misc_notes "sulfinic acid"
-xref: spec_9_group "9"
-xref: spec_9_hidden "1"
-xref: spec_9_site "U"
-xref: spec_9_position "Anywhere"
-xref: spec_9_classification "Multiple"
-xref: spec_10_group "10"
-xref: spec_10_hidden "1"
-xref: spec_10_site "E"
-xref: spec_10_position "Anywhere"
-xref: spec_10_classification "Chemical derivative"
-xref: spec_11_group "11"
-xref: spec_11_hidden "1"
-xref: spec_11_site "I"
-xref: spec_11_position "Anywhere"
-xref: spec_11_classification "Chemical derivative"
-xref: spec_12_group "12"
-xref: spec_12_hidden "1"
-xref: spec_12_site "L"
-xref: spec_12_position "Anywhere"
-xref: spec_12_classification "Chemical derivative"
-xref: spec_13_group "13"
-xref: spec_13_hidden "1"
-xref: spec_13_site "V"
-xref: spec_13_position "Anywhere"
-xref: spec_13_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:426
-name: Octanoyl
-def: "Octanoyl." [RESID:AA0290, RESID:AA0386, FindMod:OCTA, RESID:AA0584, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=426]
-xref: record_id "426"
-xref: delta_mono_mass "126.104465"
-xref: delta_avge_mass "126.1962"
-xref: delta_composition "H(14) C(8) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 18:04:46"
-xref: date_time_modified "2013-03-07 10:09:12"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "C"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:428
-name: PhosphoHexNAc
-def: "N-acetylglucosamine-1-phosphoryl." [RESID:AA0296, URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=428]
-xref: record_id "428"
-xref: delta_mono_mass "283.045704"
-xref: delta_avge_mass "283.1724"
-xref: delta_composition "H O(3) P HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 18:15:16"
-xref: date_time_modified "2015-05-01 15:11:15"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_284_mono_mass "283.045704"
-xref: spec_1_neutral_loss_284_avge_mass "283.1724"
-xref: spec_1_neutral_loss_284_flag "false"
-xref: spec_1_neutral_loss_284_composition "H O(3) P HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_284_mono_mass "283.045704"
-xref: spec_1_neutral_loss_284_avge_mass "283.1724"
-xref: spec_1_neutral_loss_284_flag "false"
-xref: spec_1_neutral_loss_284_composition "H O(3) P HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:429
-name: PhosphoHex
-def: "Phosphoglycosyl-D-mannose-1-phosphoryl." [RESID:AA0297, URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=1&hex=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=429]
-xref: record_id "429"
-xref: delta_mono_mass "242.019154"
-xref: delta_avge_mass "242.1205"
-xref: delta_composition "H O(3) P Hex"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 18:18:51"
-xref: date_time_modified "2015-05-01 15:09:57"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_243_mono_mass "242.019154"
-xref: spec_1_neutral_loss_243_avge_mass "242.1205"
-xref: spec_1_neutral_loss_243_flag "false"
-xref: spec_1_neutral_loss_243_composition "H O(3) P Hex"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_243_mono_mass "242.019154"
-xref: spec_1_neutral_loss_243_avge_mass "242.1205"
-xref: spec_1_neutral_loss_243_flag "false"
-xref: spec_1_neutral_loss_243_composition "H O(3) P Hex"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:431
-name: Palmitoleyl
-def: "Palmitoleyl." [RESID:AA0308, FindMod:PALE, PMID:17141155, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=431]
-xref: record_id "431"
-xref: delta_mono_mass "236.214016"
-xref: delta_avge_mass "236.3929"
-xref: delta_composition "H(28) C(16) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 19:57:30"
-xref: date_time_modified "2009-06-21 21:18:50"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Pre-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:432
-name: Cholesterol
-def: "Cholesterol ester." [RESID:AA0309, FindMod:CHOL, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=432]
-xref: record_id "432"
-xref: delta_mono_mass "368.344302"
-xref: delta_avge_mass "368.6383"
-xref: delta_composition "H(44) C(27)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 20:00:10"
-xref: date_time_modified "2006-10-16 16:36:21"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Protein C-term"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:433
-name: Didehydroretinylidene
-def: "3,4-didehydroretinylidene." [RESID:AA0312, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=433]
-xref: record_id "433"
-xref: delta_mono_mass "264.187801"
-xref: delta_avge_mass "264.4046"
-xref: delta_composition "H(24) C(20)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 20:05:19"
-xref: date_time_modified "2006-10-16 15:46:50"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:434
-name: CHDH
-def: "Cis-14-hydroxy-10,13-dioxo-7-heptadecenoic ester." [RESID:AA0316, FindMod:CHDH, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=434]
-xref: record_id "434"
-xref: delta_mono_mass "294.183109"
-xref: delta_avge_mass "294.3859"
-xref: delta_composition "H(26) C(17) O(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 20:08:49"
-xref: date_time_modified "2006-10-16 15:49:28"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:435
-name: Methylpyrroline
-def: "4-methyl-delta-1-pyrroline-5-carboxyl." [RESID:AA0321, FindMod:PYRK, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=435]
-xref: record_id "435"
-xref: delta_mono_mass "109.052764"
-xref: delta_avge_mass "109.1259"
-xref: delta_composition "H(7) C(6) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 20:21:00"
-xref: date_time_modified "2006-10-16 13:37:33"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:436
-name: Hydroxyheme
-def: "Hydroxyheme." [RESID:AA0324, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=436]
-xref: record_id "436"
-xref: delta_mono_mass "614.161645"
-xref: delta_avge_mass "614.4714"
-xref: delta_composition "H(30) C(34) N(4) O(4) Fe"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 20:29:16"
-xref: date_time_modified "2006-10-16 17:10:10"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:437
-name: MicrocinC7
-def: "(3-aminopropyl)(L-aspartyl-1-amino)phosphoryl-5-adenosine." [RESID:AA0328, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=437]
-xref: record_id "437"
-xref: delta_mono_mass "386.110369"
-xref: delta_avge_mass "386.3003"
-xref: delta_composition "H(19) C(13) N(6) O(6) P"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 20:36:37"
-xref: date_time_modified "2006-10-16 16:40:21"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Protein C-term"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:438
-name: Cyano
-def: "Cyano." [RESID:AA0333, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=438]
-xref: record_id "438"
-xref: delta_mono_mass "24.995249"
-xref: delta_avge_mass "25.0095"
-xref: delta_composition "H(-1) C N"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 20:42:40"
-xref: date_time_modified "2006-10-14 19:43:48"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:439
-name: Diironsubcluster
-def: "Hydrogenase diiron subcluster." [RESID:AA0334, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=439]
-xref: record_id "439"
-xref: delta_mono_mass "342.786916"
-xref: delta_avge_mass "342.876"
-xref: delta_composition "H(-1) C(5) N(2) O(5) S(2) Fe(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 20:46:03"
-xref: date_time_modified "2006-10-16 16:01:22"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:440
-name: Amidino
-def: "Amidino." [RESID:AA0335, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=440]
-xref: record_id "440"
-xref: delta_mono_mass "42.021798"
-xref: delta_avge_mass "42.04"
-xref: delta_composition "H(2) C N(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 20:49:10"
-xref: date_time_modified "2006-10-15 19:58:03"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:442
-name: FMN
-def: "O3-(riboflavin phosphoryl)." [RESID:AA0350, RESID:AA0349, FindMod:FMN, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=442]
-xref: record_id "442"
-xref: delta_mono_mass "438.094051"
-xref: delta_avge_mass "438.3285"
-xref: delta_composition "H(19) C(17) N(4) O(8) P"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 21:11:32"
-xref: date_time_modified "2006-10-16 16:47:27"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:443
-name: FMNC
-def: "S-(4a-FMN)." [RESID:AA0351, FindMod:FMNC, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=443]
-xref: record_id "443"
-xref: delta_mono_mass "456.104615"
-xref: delta_avge_mass "456.3438"
-xref: delta_composition "H(21) C(17) N(4) O(9) P"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 21:21:47"
-xref: date_time_modified "2006-10-16 16:58:10"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:444
-name: CuSMo
-def: "Copper sulfido molybdopterin cytosine dinuncleotide." [RESID:AA0355, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=444]
-xref: record_id "444"
-xref: delta_mono_mass "922.834855"
-xref: delta_avge_mass "922.067"
-xref: delta_composition "H(24) C(19) N(8) O(15) P(2) S(3) Cu Mo"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 21:34:38"
-xref: date_time_modified "2006-10-16 17:20:14"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:445
-name: Hydroxytrimethyl
-def: "5-hydroxy-N6,N6,N6-trimethyl." [RESID:AA0359, FindMod:TRIMETK, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=445]
-xref: record_id "445"
-xref: delta_mono_mass "59.04969"
-xref: delta_avge_mass "59.0871"
-xref: delta_composition "H(7) C(3) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 21:40:08"
-xref: date_time_modified "2006-10-16 10:28:02"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:447
-name: Deoxy
-def: "Reduction." [RESID:AA0191, PMID:14235557, RESID:AA0373, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=447]
-synonym: "Serine to Alanine Threonine to a-aminobutyrate" RELATED []
-xref: record_id "447"
-xref: delta_mono_mass "-15.994915"
-xref: delta_avge_mass "-15.9994"
-xref: delta_composition "O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 22:00:35"
-xref: date_time_modified "2006-10-13 17:16:30"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_2_misc_notes "Beta elimination of O-glycosylation under alkaline conditions followed by reduction"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_misc_notes "Beta elimination of O-glycosylation under alkaline conditions followed by reduction"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:448
-name: Microcin
-def: "Microcin E492 siderophore ester from serine." [RESID:AA0374, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=448]
-xref: record_id "448"
-xref: delta_mono_mass "831.197041"
-xref: delta_avge_mass "831.6871"
-xref: delta_composition "H(37) C(36) N(3) O(20)"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 22:04:46"
-xref: date_time_modified "2006-10-16 17:18:24"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Protein C-term"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:449
-name: Decanoyl
-def: "Lipid." [RESID:AA0387, RESID:AA0385, FindMod:DECA, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=449]
-xref: record_id "449"
-xref: delta_mono_mass "154.135765"
-xref: delta_avge_mass "154.2493"
-xref: delta_composition "H(18) C(10) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2005-10-15 22:14:11"
-xref: date_time_modified "2006-10-16 14:04:24"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:450
-name: Glu
-def: "Monoglutamyl." [PMID:12356754, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=450]
-xref: record_id "450"
-xref: delta_mono_mass "129.042593"
-xref: delta_avge_mass "129.114"
-xref: delta_composition "H(7) C(5) N O(3)"
-xref: username_of_poster "vcavett"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-10-18 15:07:18"
-xref: date_time_modified "2006-10-17 13:48:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Protein C-term"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "E"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:451
-name: GluGlu
-def: "Diglutamyl." [PMID:12356754, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=451]
-xref: record_id "451"
-xref: delta_mono_mass "258.085186"
-xref: delta_avge_mass "258.228"
-xref: delta_composition "H(14) C(10) N(2) O(6)"
-xref: username_of_poster "vcavett"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-10-18 15:17:59"
-xref: date_time_modified "2006-10-17 13:49:07"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Protein C-term"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "E"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:452
-name: GluGluGlu
-def: "Triglutamyl." [PMID:12356754, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=452]
-xref: record_id "452"
-xref: delta_mono_mass "387.127779"
-xref: delta_avge_mass "387.3419"
-xref: delta_composition "H(21) C(15) N(3) O(9)"
-xref: username_of_poster "vcavett"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-10-18 15:21:01"
-xref: date_time_modified "2006-10-17 14:11:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Protein C-term"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "E"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:453
-name: GluGluGluGlu
-def: "Tetraglutamyl." [PMID:12356754, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=453]
-xref: record_id "453"
-xref: delta_mono_mass "516.170373"
-xref: delta_avge_mass "516.4559"
-xref: delta_composition "H(28) C(20) N(4) O(12)"
-xref: username_of_poster "vcavett"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-10-18 15:22:24"
-xref: date_time_modified "2006-10-17 14:16:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Protein C-term"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "E"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:454
-name: HexN
-def: "Hexosamine." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hexn=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=454]
-synonym: "Glucosamine Galactosamine" RELATED []
-xref: record_id "454"
-xref: delta_mono_mass "161.068808"
-xref: delta_avge_mass "161.1558"
-xref: delta_composition "HexN"
-xref: username_of_poster "xyuan"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-11-08 18:58:20"
-xref: date_time_modified "2015-05-01 16:57:37"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Synth. pep. protect. gp."
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_162_mono_mass "161.068808"
-xref: spec_2_neutral_loss_162_avge_mass "161.1558"
-xref: spec_2_neutral_loss_162_flag "false"
-xref: spec_2_neutral_loss_162_composition "HexN"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "O-linked glycosylation"
-xref: spec_3_neutral_loss_0_mono_mass "0"
-xref: spec_3_neutral_loss_0_avge_mass "0"
-xref: spec_3_neutral_loss_0_flag "false"
-xref: spec_3_neutral_loss_0_composition "0"
-xref: spec_3_neutral_loss_162_mono_mass "161.068808"
-xref: spec_3_neutral_loss_162_avge_mass "161.1558"
-xref: spec_3_neutral_loss_162_flag "false"
-xref: spec_3_neutral_loss_162_composition "HexN"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "S"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "O-linked glycosylation"
-xref: spec_3_neutral_loss_0_mono_mass "0"
-xref: spec_3_neutral_loss_0_avge_mass "0"
-xref: spec_3_neutral_loss_0_flag "false"
-xref: spec_3_neutral_loss_0_composition "0"
-xref: spec_3_neutral_loss_162_mono_mass "161.068808"
-xref: spec_3_neutral_loss_162_avge_mass "161.1558"
-xref: spec_3_neutral_loss_162_flag "false"
-xref: spec_3_neutral_loss_162_composition "HexN"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "W"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Other glycosylation"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:455
-name: Xlink:DMP[154]
-def: "Free monolink of DMP crosslinker." [URL:http\://tools.thermofisher.com/content/sfs/manuals/MAN0011314_ImidoesterCrsLnk_DMA_DMP_DMS_DTBP_UG.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=455]
-synonym: "Dimethyl pimelimidate" RELATED []
-xref: record_id "455"
-xref: delta_mono_mass "154.110613"
-xref: delta_avge_mass "154.2096"
-xref: delta_composition "H(14) C(8) N(2) O"
-xref: username_of_poster "mariana"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-11-08 20:09:24"
-xref: date_time_modified "2017-08-18 10:27:36"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:457
-name: NDA
-def: "Naphthalene-2,3-dicarboxaldehyde." [PMID:2081203, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=457]
-comment: Fluorescent derivative.
-xref: record_id "457"
-xref: delta_mono_mass "175.042199"
-xref: delta_avge_mass "175.1855"
-xref: delta_composition "H(5) C(13) N"
-xref: username_of_poster "Dekker"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-11-11 11:03:32"
-xref: date_time_modified "2006-10-17 13:41:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:464
-name: SPITC:13C(6)
-def: "4-sulfophenyl isothiocyanate (Heavy C13)." [PMID:16526082, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=464]
-synonym: "N-terminal / lysine sulfonation" RELATED []
-xref: record_id "464"
-xref: delta_mono_mass "220.991213"
-xref: delta_avge_mass "221.2054"
-xref: delta_composition "H(5) C 13C(6) N O(3) S(2)"
-xref: username_of_poster "apanchaud"
-xref: group_of_poster "users"
-xref: date_time_posted "2005-12-19 08:37:57"
-xref: date_time_modified "2006-10-16 15:25:36"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:472
-name: AEC-MAEC
-def: "Aminoethylcysteine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=472]
-comment: Modification procedure used for phosphopeptide mapping.
-synonym: "beta-methylaminoethylcysteine" RELATED []
-xref: record_id "472"
-xref: delta_mono_mass "59.019355"
-xref: delta_avge_mass "59.1334"
-xref: delta_composition "H(5) C(2) N O(-1) S"
-xref: username_of_poster "mpcusack"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-01-20 00:46:08"
-xref: date_time_modified "2007-09-26 22:43:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "pS gives aminoethylcysteine"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_2_misc_notes "pT gives beta-methylaminoethylcysteine"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:476
-name: TMAB
-def: "4-trimethyllammoniumbutyryl-." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=476]
-xref: record_id "476"
-xref: delta_mono_mass "128.107539"
-xref: delta_avge_mass "128.1922"
-xref: delta_composition "H(14) C(7) N O"
-xref: username_of_poster "xwei"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-02-15 03:10:16"
-xref: date_time_modified "2006-10-17 12:08:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_neutral_loss_60_mono_mass "59.073499"
-xref: spec_1_neutral_loss_60_avge_mass "59.1103"
-xref: spec_1_neutral_loss_60_flag "false"
-xref: spec_1_neutral_loss_60_composition "H(9) C(3) N"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_2_neutral_loss_60_mono_mass "59.073499"
-xref: spec_2_neutral_loss_60_avge_mass "59.1103"
-xref: spec_2_neutral_loss_60_flag "false"
-xref: spec_2_neutral_loss_60_composition "H(9) C(3) N"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:477
-name: TMAB:2H(9)
-def: "D9-4-trimethyllammoniumbutyryl-." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=477]
-xref: record_id "477"
-xref: delta_mono_mass "137.16403"
-xref: delta_avge_mass "137.2476"
-xref: delta_composition "H(5) 2H(9) C(7) N O"
-xref: username_of_poster "xwei"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-02-15 18:36:06"
-xref: date_time_modified "2006-10-17 12:08:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_neutral_loss_69_mono_mass "68.12999"
-xref: spec_1_neutral_loss_69_avge_mass "68.1657"
-xref: spec_1_neutral_loss_69_flag "false"
-xref: spec_1_neutral_loss_69_composition "2H(9) C(3) N"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_2_neutral_loss_69_mono_mass "68.12999"
-xref: spec_2_neutral_loss_69_avge_mass "68.1657"
-xref: spec_2_neutral_loss_69_flag "false"
-xref: spec_2_neutral_loss_69_composition "2H(9) C(3) N"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:478
-name: FTC
-def: "Fluorescein-5-thiosemicarbazide." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=478]
-xref: record_id "478"
-xref: delta_mono_mass "421.073241"
-xref: delta_avge_mass "421.4259"
-xref: delta_composition "H(15) C(21) N(3) O(5) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2006-02-20 11:15:03"
-xref: date_time_modified "2006-10-16 16:45:27"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "P"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "R"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "S"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:481
-name: Label:2H(4)
-def: "4,4,5,5-D4 Lysine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=481]
-comment: For SILAC experiments.
-synonym: "Alanine-2,3,3,3-d4" RELATED []
-xref: record_id "481"
-xref: delta_mono_mass "4.025107"
-xref: delta_avge_mass "4.0246"
-xref: delta_composition "H(-4) 2H(4)"
-xref: username_of_poster "yunwah"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-02-20 11:44:19"
-xref: date_time_modified "2019-01-10 15:45:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "F"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Cambridge Labs DLM-451"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "A"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "485845 Aldrich"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "U"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:488
-name: DHP
-def: "Dehydropyrrolizidine alkaloid (dehydroretronecine) on cysteines." [PMID:16222722, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=488]
-synonym: "Dehydroretronecine" RELATED []
-xref: record_id "488"
-xref: delta_mono_mass "118.065674"
-xref: delta_avge_mass "118.1558"
-xref: delta_composition "H(8) C(8) N"
-xref: username_of_poster "rowanrainbow"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-03-07 08:40:13"
-xref: date_time_modified "2006-10-17 12:07:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:490
-name: Hep
-def: "Heptose." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=490]
-xref: record_id "490"
-xref: delta_mono_mass "192.063388"
-xref: delta_avge_mass "192.1666"
-xref: delta_composition "Hep"
-xref: username_of_poster "anikolakakis"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-03-24 15:59:43"
-xref: date_time_modified "2015-05-05 15:58:34"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other glycosylation"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_193_mono_mass "192.063388"
-xref: spec_2_neutral_loss_193_avge_mass "192.1666"
-xref: spec_2_neutral_loss_193_flag "false"
-xref: spec_2_neutral_loss_193_composition "Hep"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Q"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Other glycosylation"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "R"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "N-linked glycosylation"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "T"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "O-linked glycosylation"
-xref: spec_5_neutral_loss_193_mono_mass "192.063388"
-xref: spec_5_neutral_loss_193_avge_mass "192.1666"
-xref: spec_5_neutral_loss_193_flag "false"
-xref: spec_5_neutral_loss_193_composition "Hep"
-xref: spec_5_neutral_loss_0_mono_mass "0"
-xref: spec_5_neutral_loss_0_avge_mass "0"
-xref: spec_5_neutral_loss_0_flag "false"
-xref: spec_5_neutral_loss_0_composition "0"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "S"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "O-linked glycosylation"
-xref: spec_5_neutral_loss_193_mono_mass "192.063388"
-xref: spec_5_neutral_loss_193_avge_mass "192.1666"
-xref: spec_5_neutral_loss_193_flag "false"
-xref: spec_5_neutral_loss_193_composition "Hep"
-xref: spec_5_neutral_loss_0_mono_mass "0"
-xref: spec_5_neutral_loss_0_avge_mass "0"
-xref: spec_5_neutral_loss_0_flag "false"
-xref: spec_5_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:493
-name: BADGE
-def: "Bisphenol A diglycidyl ether derivative." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=493]
-comment: Found in canned food products.
-xref: record_id "493"
-xref: delta_mono_mass "340.167459"
-xref: delta_avge_mass "340.4129"
-xref: delta_composition "H(24) C(21) O(4)"
-xref: username_of_poster "TNO"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-03-27 09:30:54"
-xref: date_time_modified "2006-10-17 14:09:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Non-standard residue"
-xref: spec_1_misc_notes "found in canned food products"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:494
-name: CyDye-Cy3
-def: "Cy3 CyDye DIGE Fluor saturation dye." [PMID:12872219, URL:https\://www.gelifesciences.com/gehcls_images/GELS/Related%20Content/Files/1314735988470/litdoc28953107AD_20110831002141.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=494]
-synonym: "Formula needs confirmation" RELATED []
-xref: record_id "494"
-xref: delta_mono_mass "672.298156"
-xref: delta_avge_mass "672.8335"
-xref: delta_composition "H(44) C(37) N(4) O(6) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2006-03-27 11:17:51"
-xref: date_time_modified "2012-09-15 00:20:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:495
-name: CyDye-Cy5
-def: "Cy5 CyDye DIGE Fluor saturation dye." [PMID:12872219, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=495]
-xref: record_id "495"
-xref: delta_mono_mass "684.298156"
-xref: delta_avge_mass "684.8442"
-xref: delta_composition "H(44) C(38) N(4) O(6) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2006-03-27 11:53:04"
-xref: date_time_modified "2006-10-17 14:18:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:498
-name: BHTOH
-def: "Michael addition of t-butyl hydroxylated BHT (BHTOH) to C, H or K." [PMID:16533022, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=498]
-comment: BHTOH is formed upon metabolism of BHT with P450 enzymes. The BHTOH is further metabolized to its quinone methide (electrophile) which reacts with -SH and -NH2 groups.
-synonym: "t-butyl hydroxylated BHT" RELATED []
-xref: record_id "498"
-xref: delta_mono_mass "234.16198"
-xref: delta_avge_mass "234.334"
-xref: delta_composition "H(22) C(15) O(2)"
-xref: username_of_poster "rkupfer"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-04-10 19:27:51"
-xref: date_time_modified "2006-10-17 13:42:22"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_1_misc_notes "primary adduct"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Other"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:499
-name: IGBP:13C(2)
-def: "Heavy IDBEST tag for quantitation." [URL:http\://www.targetdiscovery.com/index.php?topic=prod.idbe, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=499]
-xref: record_id "499"
-xref: delta_mono_mass "298.022748"
-xref: delta_avge_mass "299.1331"
-xref: delta_composition "H(13) C(10) 13C(2) N(2) O(2) Br"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2006-04-14 18:44:41"
-xref: date_time_modified "2006-10-19 10:48:25"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:500
-name: Nmethylmaleimide+water
-def: "Nmethylmaleimidehydrolysis." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=500]
-xref: record_id "500"
-xref: delta_mono_mass "129.042593"
-xref: delta_avge_mass "129.114"
-xref: delta_composition "H(7) C(5) N O(3)"
-xref: username_of_poster "whaskins"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-04-14 22:58:34"
-xref: date_time_modified "2006-10-17 12:12:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:501
-name: PyMIC
-def: "3-methyl-2-pyridyl isocyanate." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=501]
-xref: record_id "501"
-xref: delta_mono_mass "134.048013"
-xref: delta_avge_mass "134.1353"
-xref: delta_composition "H(6) C(7) N(2) O"
-xref: username_of_poster "TING"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-04-18 20:46:17"
-xref: date_time_modified "2006-10-17 12:19:15"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:503
-name: LG-lactam-K
-def: "Levuglandinyl - lysine lactam adduct." [PMID:15650407, PMID:15752459, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=503]
-xref: record_id "503"
-xref: delta_mono_mass "332.19876"
-xref: delta_avge_mass "332.4339"
-xref: delta_composition "H(28) C(20) O(4)"
-xref: username_of_poster "alexparf"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-04-27 17:56:39"
-xref: date_time_modified "2006-11-14 12:04:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:504
-name: LG-Hlactam-K
-def: "Levuglandinyl - lysine hydroxylactam adduct." [PMID:15650407, PMID:15752459, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=504]
-xref: record_id "504"
-xref: delta_mono_mass "348.193674"
-xref: delta_avge_mass "348.4333"
-xref: delta_composition "H(28) C(20) O(5)"
-xref: username_of_poster "alexparf"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-04-27 18:02:17"
-xref: date_time_modified "2006-11-14 12:04:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:505
-name: LG-lactam-R
-def: "Levuglandinyl - arginine lactam adduct." [PMID:15650407, PMID:15752459, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=505]
-xref: record_id "505"
-xref: delta_mono_mass "290.176961"
-xref: delta_avge_mass "290.3939"
-xref: delta_composition "H(26) C(19) N(-2) O(4)"
-xref: username_of_poster "alexparf"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-04-27 18:05:11"
-xref: date_time_modified "2006-10-17 14:08:20"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:506
-name: LG-Hlactam-R
-def: "Levuglandinyl - arginine hydroxylactam adduct." [PMID:15650407, PMID:15752459, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=506]
-xref: record_id "506"
-xref: delta_mono_mass "306.171876"
-xref: delta_avge_mass "306.3933"
-xref: delta_composition "H(26) C(19) N(-2) O(5)"
-xref: username_of_poster "alexparf"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-04-27 18:08:11"
-xref: date_time_modified "2006-10-17 14:08:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:510
-name: Dimethyl:2H(4)13C(2)
-def: "DiMethyl-C13HD2." [PMID:16335955, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=510]
-xref: record_id "510"
-xref: delta_mono_mass "34.063117"
-xref: delta_avge_mass "34.0631"
-xref: delta_composition "2H(4) 13C(2)"
-xref: username_of_poster "oded"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-05-08 22:03:41"
-xref: date_time_modified "2014-11-16 07:37:20"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "R"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "N-term"
-xref: spec_4_position "Protein N-term"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "When dimethyl labelling is pre-digest"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:512
-name: Hex(2)
-def: "Lactosylation." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=512]
-comment: Lactosylation of bovine Beta-Lactoglobulin.
-synonym: "lac" RELATED []
-xref: record_id "512"
-xref: delta_mono_mass "324.105647"
-xref: delta_avge_mass "324.2812"
-xref: delta_composition "Hex(2)"
-xref: username_of_poster "molle"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-05-11 13:21:17"
-xref: date_time_modified "2017-11-23 12:59:14"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other glycosylation"
-xref: spec_1_misc_notes "Maillard reaction (first event)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "R"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Other glycosylation"
-xref: spec_2_misc_notes "Maillard reaction (first event)"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "S"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "O-linked glycosylation"
-xref: spec_3_neutral_loss_0_mono_mass "0"
-xref: spec_3_neutral_loss_0_avge_mass "0"
-xref: spec_3_neutral_loss_0_flag "false"
-xref: spec_3_neutral_loss_0_composition "0"
-xref: spec_3_neutral_loss_325_mono_mass "324.105647"
-xref: spec_3_neutral_loss_325_avge_mass "324.2812"
-xref: spec_3_neutral_loss_325_flag "false"
-xref: spec_3_neutral_loss_325_composition "Hex(2)"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "O-linked glycosylation"
-xref: spec_3_neutral_loss_0_mono_mass "0"
-xref: spec_3_neutral_loss_0_avge_mass "0"
-xref: spec_3_neutral_loss_0_flag "false"
-xref: spec_3_neutral_loss_0_composition "0"
-xref: spec_3_neutral_loss_325_mono_mass "324.105647"
-xref: spec_3_neutral_loss_325_avge_mass "324.2812"
-xref: spec_3_neutral_loss_325_flag "false"
-xref: spec_3_neutral_loss_325_composition "Hex(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:513
-name: C8-QAT
-def: "[3-(2,5)-Dioxopyrrolidin-1-yloxycarbonyl)-propyl]dimethyloctylammonium." [PMID:16771548, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=513]
-xref: record_id "513"
-xref: delta_mono_mass "227.224915"
-xref: delta_avge_mass "227.3862"
-xref: delta_composition "H(29) C(14) N O"
-xref: username_of_poster "amadian"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-05-13 20:55:20"
-xref: date_time_modified "2006-12-03 19:43:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:514
-name: PropylNAGthiazoline
-def: "Propyl-1,2-dideoxy-2\'-methyl-alpha-D-glucopyranoso-[2,1-d]-Delta2\'-thiazoline." [PMID:15795231, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=514]
-comment: In a recent publication (see reference), we have shown that family 84 glycoside hydrolases contain a deep pocket beneath the 2-acetamido group of its substrate (N-acetyl-glucosamine). With this strucual feature in mind, we have designed a specific inhibitor that contains a chloride group appended to the end of the propyl chain on a known inhibitor termed propyl-NAG-thiazoline. We have shown kinetically that this molecule is a potent suicide inhibitor of this enzyme famiy and now wish to know the precise residue which is acting as the nucleophile to dispace the choride atom. We have included all residues that are in the vacinity of the chloride atom that could potentially act in a nucleophilic manner.
-xref: record_id "514"
-xref: delta_mono_mass "232.064354"
-xref: delta_avge_mass "232.2768"
-xref: delta_composition "H(14) C(9) N O(4) S"
-xref: username_of_poster "mmacaule"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-05-18 18:44:52"
-xref: date_time_modified "2015-05-01 13:33:58"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:515
-name: FNEM
-def: "Fluorescein-5-maleimide." [PMID:9325338, PMID:11665566, URL:http\://probes.invitrogen.com/media/pis/mp00003.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=515]
-synonym: "fluorescein-NEM" RELATED []
-xref: record_id "515"
-xref: delta_mono_mass "427.069202"
-xref: delta_avge_mass "427.3625"
-xref: delta_composition "H(13) C(24) N O(7)"
-xref: username_of_poster "shure"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-06-08 10:07:56"
-xref: date_time_modified "2006-10-17 14:15:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "photosensitive"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:518
-name: Diethyl
-def: "Diethylation, analogous to Dimethylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=518]
-xref: record_id "518"
-xref: delta_mono_mass "56.0626"
-xref: delta_avge_mass "56.1063"
-xref: delta_composition "H(8) C(4)"
-xref: username_of_poster "PhilipHsu"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-06-15 07:18:26"
-xref: date_time_modified "2006-10-17 12:00:33"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:519
-name: BisANS
-def: "4,4\'-dianilino-1,1\'-binaphthyl-5,5\'-disulfonic acid." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=519]
-xref: record_id "519"
-xref: delta_mono_mass "594.091928"
-xref: delta_avge_mass "594.6569"
-xref: delta_composition "H(22) C(32) N(2) O(6) S(2)"
-xref: username_of_poster "app95d"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-07-05 23:31:08"
-xref: date_time_modified "2012-05-15 20:15:06"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:520
-name: Piperidine
-def: "Piperidination." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=520]
-xref: record_id "520"
-xref: delta_mono_mass "68.0626"
-xref: delta_avge_mass "68.117"
-xref: delta_composition "H(8) C(5)"
-xref: username_of_poster "PhilipHsu"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-07-20 08:37:21"
-xref: date_time_modified "2006-10-17 12:05:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:522
-name: Maleimide-PEO2-Biotin
-def: "Maleimide-Biotin." [URL:http\://www.piercenet.com/Products/Browse.cfm?fldID=01031005, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=522]
-synonym: "Maleimide-PEG2-Biotin" RELATED []
-xref: record_id "522"
-xref: delta_mono_mass "525.225719"
-xref: delta_avge_mass "525.6183"
-xref: delta_composition "H(35) C(23) N(5) O(7) S"
-xref: username_of_poster "ericjohansen"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-08-11 02:49:51"
-xref: date_time_modified "2010-12-03 16:13:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:523
-name: Sulfo-NHS-LC-LC-Biotin
-def: "Biot_LC_LC." [URL:http\://www.piercenet.com/Products/Browse.cfm?fldID=8D38BA83-EFDC-421A-853F-E96EBA380612, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=523]
-synonym: "Sulfo-NHS-LC-LC-Biotin" RELATED []
-xref: record_id "523"
-xref: delta_mono_mass "452.245726"
-xref: delta_avge_mass "452.6106"
-xref: delta_composition "H(36) C(22) N(4) O(4) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster "admin"
-xref: date_time_posted "2006-08-31 18:01:50"
-xref: date_time_modified "2010-12-03 16:11:08"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:525
-name: CLIP_TRAQ_2
-def: "CLIP_TRAQ_2." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=525]
-comment: CLIP-TRAQ-2 H(17) C(10) C13 N(3) O(4) is an in-house made compound that reacts with primary amines through a N-hydroxysuccinimide group leading to a 141.0983 Da mass shift (monoisotopic) in MS mode. The reporter ion in MS/MS mode can either be 113 or 114 m/z depending on the position of isotopic C13 in the molecule. (Fahlman, R. and Overall, C.M. ; in preparation).
-synonym: "CLIP_TRAQ_double" RELATED []
-xref: record_id "525"
-xref: delta_mono_mass "141.098318"
-xref: delta_avge_mass "141.1756"
-xref: delta_composition "H(12) C(6) 13C N(2) O"
-xref: username_of_poster "overalllab"
-xref: group_of_poster "users"
-xref: date_time_posted "2006-09-15 02:25:46"
-xref: date_time_modified "2006-10-17 18:04:46"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Side reaction, low abundance"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:526
-name: Dethiomethyl
-def: "Prompt loss of side chain from oxidised Met." [PMID:9004526, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=526]
-comment: More commonly seen as a neutral loss.
-xref: record_id "526"
-xref: delta_mono_mass "-48.003371"
-xref: delta_avge_mass "-48.1075"
-xref: delta_composition "H(-4) C(-1) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-10-13 15:14:55"
-xref: date_time_modified "2006-10-13 17:02:27"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:528
-name: Methyl+Deamidated
-def: "Deamidation followed by a methylation." [FindMod:DEAME, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=528]
-synonym: "Glutamate methyl ester" RELATED []
-xref: record_id "528"
-xref: delta_mono_mass "14.999666"
-xref: delta_avge_mass "15.0113"
-xref: delta_composition "H C N(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-10-14 10:39:08"
-xref: date_time_modified "2007-02-04 12:25:42"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:529
-name: Delta:H(5)C(2)
-def: "Dimethylation of proline residue." [FindMod:DIMETP, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=529]
-xref: record_id "529"
-xref: delta_mono_mass "29.039125"
-xref: delta_avge_mass "29.0611"
-xref: delta_composition "H(5) C(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-10-15 18:02:34"
-xref: date_time_modified "2006-10-15 18:03:16"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:530
-name: Cation:K
-def: "Replacement of proton by potassium." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=530]
-xref: record_id "530"
-xref: delta_mono_mass "37.955882"
-xref: delta_avge_mass "38.0904"
-xref: delta_composition "H(-1) K"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-10-15 18:29:43"
-xref: date_time_modified "2006-10-18 11:17:39"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:531
-name: Cation:Cu[I]
-def: "Replacement of proton by copper." [URL:http\://www.uniprot.org/uniprot/P07509, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=531]
-xref: record_id "531"
-xref: delta_mono_mass "61.921774"
-xref: delta_avge_mass "62.5381"
-xref: delta_composition "H(-1) Cu"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-10-16 10:29:12"
-xref: date_time_modified "2015-03-19 09:33:03"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "H"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:532
-name: iTRAQ4plex114
-def: "Accurate mass for 114." [URL:http\://docs.appliedbiosystems.com/pebiodocs/04351918.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=532]
-comment: Different channels have the same nominal mass but slightly different exact masses.
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED []
-xref: record_id "532"
-xref: delta_mono_mass "144.105918"
-xref: delta_avge_mass "144.168"
-xref: delta_composition "H(12) C(5) 13C(2) N(2) 18O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-10-16 13:46:49"
-xref: date_time_modified "2024-08-12 09:55:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Low abundance"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "C"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "side reaction"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:533
-name: iTRAQ4plex115
-def: "Accurate mass for 115." [URL:http\://docs.appliedbiosystems.com/pebiodocs/04351918.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=533]
-comment: Different channels have the same nominal mass but slightly different exact masses.
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED []
-xref: record_id "533"
-xref: delta_mono_mass "144.099599"
-xref: delta_avge_mass "144.1688"
-xref: delta_composition "H(12) C(6) 13C N 15N 18O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-10-16 13:48:16"
-xref: date_time_modified "2024-08-12 09:55:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Low abundance"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "C"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "side reaction"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:534
-name: Dibromo
-def: "Dibromo." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=534]
-xref: record_id "534"
-xref: delta_mono_mass "155.821022"
-xref: delta_avge_mass "157.7921"
-xref: delta_composition "H(-2) Br(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-10-16 14:06:38"
-xref: date_time_modified "2006-10-16 14:06:38"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:535
-name: LRGG
-def: "Ubiquitination." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=535]
-synonym: "Addition of LRGG" RELATED []
-xref: record_id "535"
-xref: delta_mono_mass "383.228103"
-xref: delta_avge_mass "383.446"
-xref: delta_composition "H(29) C(16) N(7) O(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-10-16 16:39:05"
-xref: date_time_modified "2014-07-09 16:48:40"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:536
-name: CLIP_TRAQ_3
-def: "CLIP_TRAQ_3." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=536]
-comment: CLIP_TRAQ_3 (H(20) C(11) C13 N(3) O(4) is an in-house made compound that reacts with primary amines through a N-hydroxysuccinimide group leading to a 155.1 Da mass shift (monoisotopic) in MS mode. The reporter ion in MS/MS mode can either be 127 or 128 m/z depending on the position of isotopic C13 in the molecule. (Fahlman, R. and Overall, C.M. ; in preparation).
-xref: record_id "536"
-xref: delta_mono_mass "271.148736"
-xref: delta_avge_mass "271.2976"
-xref: delta_composition "H(20) C(11) 13C N(3) O(4)"
-xref: username_of_poster "overall"
-xref: group_of_poster ""
-xref: date_time_posted "2006-10-17 18:08:00"
-xref: date_time_modified "2006-10-17 18:11:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Low abundance"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:537
-name: CLIP_TRAQ_4
-def: "CLIP_TRAQ_4." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=537]
-comment: CLIP_TRAQ_4 is an in-house made compound that reacts with primary amines through a N-hydroxysuccinimide group leading to a 128.1 Da mass shift (monoisotopic) in MS mode. The reporter ion in MS/MS mode can either be 100 or 101 m/z depending on the position of isotopic C13 in the molecule. (Fahlman, R. and Overall, C.M. ; in preparation).
-xref: record_id "537"
-xref: delta_mono_mass "244.101452"
-xref: delta_avge_mass "244.2292"
-xref: delta_composition "H(15) C(9) 13C N(2) O(5)"
-xref: username_of_poster "overall"
-xref: group_of_poster ""
-xref: date_time_posted "2006-10-17 18:09:22"
-xref: date_time_modified "2006-10-17 18:10:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Low abundance"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:538
-name: Biotin:Cayman-10141
-def: "Was 15dB-biotin." [URL:http\://www.caymanchem.com/pdfs/10141.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=538]
-synonym: "15-deoxy-delta 12,14-Prostaglandin J2-biotinimide" RELATED []
-xref: record_id "538"
-xref: delta_mono_mass "626.386577"
-xref: delta_avge_mass "626.8927"
-xref: delta_composition "H(54) C(35) N(4) O(4) S"
-xref: username_of_poster "sevgh"
-xref: group_of_poster ""
-xref: date_time_posted "2006-10-17 18:13:45"
-xref: date_time_modified "2010-12-03 16:08:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:539
-name: Biotin:Cayman-10013
-def: "Was PGA1-biotin." [URL:http\://www.caymanchem.com/pdfs/10013.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=539]
-synonym: "Prostaglandin A1-biotinimide" RELATED []
-xref: record_id "539"
-xref: delta_mono_mass "660.428442"
-xref: delta_avge_mass "660.9504"
-xref: delta_composition "H(60) C(36) N(4) O(5) S"
-xref: username_of_poster "sevgh"
-xref: group_of_poster ""
-xref: date_time_posted "2006-10-17 18:24:06"
-xref: date_time_modified "2010-12-03 16:07:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:540
-name: Ala->Ser
-def: "Ala->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=540]
-xref: record_id "540"
-xref: delta_mono_mass "15.994915"
-xref: delta_avge_mass "15.9994"
-xref: delta_composition "O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:07:30"
-xref: date_time_modified "2006-11-09 10:07:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:541
-name: Ala->Thr
-def: "Ala->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=541]
-xref: record_id "541"
-xref: delta_mono_mass "30.010565"
-xref: delta_avge_mass "30.026"
-xref: delta_composition "H(2) C O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:13:43"
-xref: date_time_modified "2006-11-09 10:13:43"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:542
-name: Ala->Asp
-def: "Ala->Asp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=542]
-xref: record_id "542"
-xref: delta_mono_mass "43.989829"
-xref: delta_avge_mass "44.0095"
-xref: delta_composition "C O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:15:05"
-xref: date_time_modified "2006-11-09 10:15:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:543
-name: Ala->Pro
-def: "Ala->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=543]
-xref: record_id "543"
-xref: delta_mono_mass "26.01565"
-xref: delta_avge_mass "26.0373"
-xref: delta_composition "H(2) C(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:16:03"
-xref: date_time_modified "2006-11-09 10:16:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:544
-name: Ala->Gly
-def: "Ala->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=544]
-xref: record_id "544"
-xref: delta_mono_mass "-14.01565"
-xref: delta_avge_mass "-14.0266"
-xref: delta_composition "H(-2) C(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:16:35"
-xref: date_time_modified "2006-11-09 10:16:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:545
-name: Ala->Glu
-def: "Ala->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=545]
-xref: record_id "545"
-xref: delta_mono_mass "58.005479"
-xref: delta_avge_mass "58.0361"
-xref: delta_composition "H(2) C(2) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:19:56"
-xref: date_time_modified "2006-11-09 10:19:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:546
-name: Ala->Val
-def: "Ala->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=546]
-xref: record_id "546"
-xref: delta_mono_mass "28.0313"
-xref: delta_avge_mass "28.0532"
-xref: delta_composition "H(4) C(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:20:15"
-xref: date_time_modified "2006-11-09 10:20:15"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:547
-name: Cys->Phe
-def: "Cys->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=547]
-xref: record_id "547"
-xref: delta_mono_mass "44.059229"
-xref: delta_avge_mass "44.031"
-xref: delta_composition "H(4) C(6) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:20:41"
-xref: date_time_modified "2006-11-09 10:20:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:548
-name: Cys->Ser
-def: "Cys->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=548]
-xref: record_id "548"
-xref: delta_mono_mass "-15.977156"
-xref: delta_avge_mass "-16.0656"
-xref: delta_composition "O S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:21:13"
-xref: date_time_modified "2006-11-09 10:21:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:549
-name: Cys->Trp
-def: "Cys->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=549]
-xref: record_id "549"
-xref: delta_mono_mass "83.070128"
-xref: delta_avge_mass "83.067"
-xref: delta_composition "H(5) C(8) N S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:21:37"
-xref: date_time_modified "2006-11-09 10:21:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:550
-name: Cys->Tyr
-def: "Cys->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=550]
-xref: record_id "550"
-xref: delta_mono_mass "60.054144"
-xref: delta_avge_mass "60.0304"
-xref: delta_composition "H(4) C(6) O S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:22:04"
-xref: date_time_modified "2006-11-09 10:22:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:551
-name: Cys->Arg
-def: "Cys->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=551]
-xref: record_id "551"
-xref: delta_mono_mass "53.091927"
-xref: delta_avge_mass "53.0428"
-xref: delta_composition "H(7) C(3) N(3) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:22:25"
-xref: date_time_modified "2006-11-09 10:22:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:552
-name: Cys->Gly
-def: "Cys->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=552]
-xref: record_id "552"
-xref: delta_mono_mass "-45.987721"
-xref: delta_avge_mass "-46.0916"
-xref: delta_composition "H(-2) C(-1) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:22:43"
-xref: date_time_modified "2006-11-09 10:22:43"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:553
-name: Asp->Ala
-def: "Asp->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=553]
-xref: record_id "553"
-xref: delta_mono_mass "-43.989829"
-xref: delta_avge_mass "-44.0095"
-xref: delta_composition "C(-1) O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:53:54"
-xref: date_time_modified "2006-11-09 10:53:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:554
-name: Asp->His
-def: "Asp->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=554]
-xref: record_id "554"
-xref: delta_mono_mass "22.031969"
-xref: delta_avge_mass "22.0519"
-xref: delta_composition "H(2) C(2) N(2) O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:55:25"
-xref: date_time_modified "2006-11-09 10:55:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:555
-name: Asp->Asn
-def: "Asp->Asn substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=555]
-xref: record_id "555"
-xref: delta_mono_mass "-0.984016"
-xref: delta_avge_mass "-0.9848"
-xref: delta_composition "H N O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:55:49"
-xref: date_time_modified "2006-11-09 10:55:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:556
-name: Asp->Gly
-def: "Asp->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=556]
-xref: record_id "556"
-xref: delta_mono_mass "-58.005479"
-xref: delta_avge_mass "-58.0361"
-xref: delta_composition "H(-2) C(-2) O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:56:52"
-xref: date_time_modified "2006-11-09 10:56:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:557
-name: Asp->Tyr
-def: "Asp->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=557]
-xref: record_id "557"
-xref: delta_mono_mass "48.036386"
-xref: delta_avge_mass "48.0859"
-xref: delta_composition "H(4) C(5) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:58:23"
-xref: date_time_modified "2006-11-09 10:58:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:558
-name: Asp->Glu
-def: "Asp->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=558]
-xref: record_id "558"
-xref: delta_mono_mass "14.01565"
-xref: delta_avge_mass "14.0266"
-xref: delta_composition "H(2) C"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:58:44"
-xref: date_time_modified "2006-11-09 10:58:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:559
-name: Asp->Val
-def: "Asp->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=559]
-xref: record_id "559"
-xref: delta_mono_mass "-15.958529"
-xref: delta_avge_mass "-15.9563"
-xref: delta_composition "H(4) C O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 10:59:02"
-xref: date_time_modified "2006-11-09 10:59:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:560
-name: Glu->Ala
-def: "Glu->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=560]
-xref: record_id "560"
-xref: delta_mono_mass "-58.005479"
-xref: delta_avge_mass "-58.0361"
-xref: delta_composition "H(-2) C(-2) O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:00:54"
-xref: date_time_modified "2006-11-09 11:00:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:561
-name: Glu->Gln
-def: "Glu->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=561]
-xref: record_id "561"
-xref: delta_mono_mass "-0.984016"
-xref: delta_avge_mass "-0.9848"
-xref: delta_composition "H N O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:01:29"
-xref: date_time_modified "2006-11-09 11:01:29"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:562
-name: Glu->Asp
-def: "Glu->Asp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=562]
-xref: record_id "562"
-xref: delta_mono_mass "-14.01565"
-xref: delta_avge_mass "-14.0266"
-xref: delta_composition "H(-2) C(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:01:53"
-xref: date_time_modified "2006-11-09 11:01:53"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:563
-name: Glu->Lys
-def: "Glu->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=563]
-xref: record_id "563"
-xref: delta_mono_mass "-0.94763"
-xref: delta_avge_mass "-0.9417"
-xref: delta_composition "H(5) C N O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:02:15"
-xref: date_time_modified "2006-11-09 11:02:15"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:564
-name: Glu->Gly
-def: "Glu->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=564]
-xref: record_id "564"
-xref: delta_mono_mass "-72.021129"
-xref: delta_avge_mass "-72.0627"
-xref: delta_composition "H(-4) C(-3) O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:02:36"
-xref: date_time_modified "2006-11-09 11:02:36"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:565
-name: Glu->Val
-def: "Glu->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=565]
-xref: record_id "565"
-xref: delta_mono_mass "-29.974179"
-xref: delta_avge_mass "-29.9829"
-xref: delta_composition "H(2) O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:03:02"
-xref: date_time_modified "2006-11-09 11:03:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:566
-name: Phe->Ser
-def: "Phe->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=566]
-xref: record_id "566"
-xref: delta_mono_mass "-60.036386"
-xref: delta_avge_mass "-60.0966"
-xref: delta_composition "H(-4) C(-6) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:03:29"
-xref: date_time_modified "2006-11-09 11:03:29"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:567
-name: Phe->Cys
-def: "Phe->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=567]
-xref: record_id "567"
-xref: delta_mono_mass "-44.059229"
-xref: delta_avge_mass "-44.031"
-xref: delta_composition "H(-4) C(-6) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:04:01"
-xref: date_time_modified "2006-11-09 11:04:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:568
-name: Phe->Xle
-def: "Phe->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=568]
-xref: record_id "568"
-xref: delta_mono_mass "-33.98435"
-xref: delta_avge_mass "-34.0162"
-xref: delta_composition "H(2) C(-3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:05:41"
-xref: date_time_modified "2011-06-21 15:10:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:569
-name: Phe->Tyr
-def: "Phe->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=569]
-xref: record_id "569"
-xref: delta_mono_mass "15.994915"
-xref: delta_avge_mass "15.9994"
-xref: delta_composition "O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:06:56"
-xref: date_time_modified "2006-11-09 11:06:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:570
-name: Phe->Val
-def: "Phe->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=570]
-xref: record_id "570"
-xref: delta_mono_mass "-48"
-xref: delta_avge_mass "-48.0428"
-xref: delta_composition "C(-4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:07:20"
-xref: date_time_modified "2006-11-09 11:07:20"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:571
-name: Gly->Ala
-def: "Gly->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=571]
-xref: record_id "571"
-xref: delta_mono_mass "14.01565"
-xref: delta_avge_mass "14.0266"
-xref: delta_composition "H(2) C"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:07:51"
-xref: date_time_modified "2006-11-09 11:07:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:572
-name: Gly->Ser
-def: "Gly->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=572]
-xref: record_id "572"
-xref: delta_mono_mass "30.010565"
-xref: delta_avge_mass "30.026"
-xref: delta_composition "H(2) C O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:08:13"
-xref: date_time_modified "2006-11-09 11:08:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:573
-name: Gly->Trp
-def: "Gly->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=573]
-xref: record_id "573"
-xref: delta_mono_mass "129.057849"
-xref: delta_avge_mass "129.1586"
-xref: delta_composition "H(7) C(9) N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:08:33"
-xref: date_time_modified "2006-11-09 11:08:33"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:574
-name: Gly->Glu
-def: "Gly->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=574]
-xref: record_id "574"
-xref: delta_mono_mass "72.021129"
-xref: delta_avge_mass "72.0627"
-xref: delta_composition "H(4) C(3) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:08:57"
-xref: date_time_modified "2006-11-09 11:08:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:575
-name: Gly->Val
-def: "Gly->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=575]
-xref: record_id "575"
-xref: delta_mono_mass "42.04695"
-xref: delta_avge_mass "42.0797"
-xref: delta_composition "H(6) C(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:09:18"
-xref: date_time_modified "2006-11-09 11:09:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:576
-name: Gly->Asp
-def: "Gly->Asp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=576]
-xref: record_id "576"
-xref: delta_mono_mass "58.005479"
-xref: delta_avge_mass "58.0361"
-xref: delta_composition "H(2) C(2) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:09:44"
-xref: date_time_modified "2006-11-09 11:09:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:577
-name: Gly->Cys
-def: "Gly->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=577]
-xref: record_id "577"
-xref: delta_mono_mass "45.987721"
-xref: delta_avge_mass "46.0916"
-xref: delta_composition "H(2) C S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:10:03"
-xref: date_time_modified "2006-11-09 11:10:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:578
-name: Gly->Arg
-def: "Gly->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=578]
-xref: record_id "578"
-xref: delta_mono_mass "99.079647"
-xref: delta_avge_mass "99.1344"
-xref: delta_composition "H(9) C(4) N(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:10:23"
-xref: date_time_modified "2006-11-09 11:10:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:580
-name: His->Pro
-def: "His->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=580]
-xref: record_id "580"
-xref: delta_mono_mass "-40.006148"
-xref: delta_avge_mass "-40.0241"
-xref: delta_composition "C(-1) N(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:11:29"
-xref: date_time_modified "2006-11-09 11:11:29"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:581
-name: His->Tyr
-def: "His->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=581]
-xref: record_id "581"
-xref: delta_mono_mass "26.004417"
-xref: delta_avge_mass "26.034"
-xref: delta_composition "H(2) C(3) N(-2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:11:50"
-xref: date_time_modified "2006-11-09 11:11:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:582
-name: His->Gln
-def: "His->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=582]
-xref: record_id "582"
-xref: delta_mono_mass "-9.000334"
-xref: delta_avge_mass "-9.0101"
-xref: delta_composition "H C(-1) N(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:14:42"
-xref: date_time_modified "2006-11-09 11:14:42"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:584
-name: His->Arg
-def: "His->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=584]
-xref: record_id "584"
-xref: delta_mono_mass "19.042199"
-xref: delta_avge_mass "19.0464"
-xref: delta_composition "H(5) N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:15:26"
-xref: date_time_modified "2006-11-09 11:15:26"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:585
-name: His->Xle
-def: "His->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=585]
-xref: record_id "585"
-xref: delta_mono_mass "-23.974848"
-xref: delta_avge_mass "-23.9816"
-xref: delta_composition "H(4) N(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:15:51"
-xref: date_time_modified "2011-06-21 15:10:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:588
-name: Xle->Thr
-def: "Leu/Ile->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=588]
-xref: record_id "588"
-xref: delta_mono_mass "-12.036386"
-xref: delta_avge_mass "-12.0538"
-xref: delta_composition "H(-4) C(-2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:18:09"
-xref: date_time_modified "2011-06-21 15:29:22"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "I"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "L"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:589
-name: Xle->Asn
-def: "Leu/Ile->Asn substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=589]
-xref: record_id "589"
-xref: delta_mono_mass "0.958863"
-xref: delta_avge_mass "0.945"
-xref: delta_composition "H(-5) C(-2) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:18:31"
-xref: date_time_modified "2011-06-21 15:29:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "I"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "L"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:590
-name: Xle->Lys
-def: "Leu/Ile->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=590]
-xref: record_id "590"
-xref: delta_mono_mass "15.010899"
-xref: delta_avge_mass "15.0146"
-xref: delta_composition "H N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:18:57"
-xref: date_time_modified "2011-06-21 15:27:59"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "I"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "L"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:594
-name: Lys->Thr
-def: "Lys->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=594]
-xref: record_id "594"
-xref: delta_mono_mass "-27.047285"
-xref: delta_avge_mass "-27.0684"
-xref: delta_composition "H(-5) C(-2) N(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:20:28"
-xref: date_time_modified "2006-11-09 11:20:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:595
-name: Lys->Asn
-def: "Lys->Asn substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=595]
-xref: record_id "595"
-xref: delta_mono_mass "-14.052036"
-xref: delta_avge_mass "-14.0696"
-xref: delta_composition "H(-6) C(-2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:20:51"
-xref: date_time_modified "2006-11-09 11:20:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:596
-name: Lys->Glu
-def: "Lys->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=596]
-xref: record_id "596"
-xref: delta_mono_mass "0.94763"
-xref: delta_avge_mass "0.9417"
-xref: delta_composition "H(-5) C(-1) N(-1) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:21:12"
-xref: date_time_modified "2006-11-09 11:21:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:597
-name: Lys->Gln
-def: "Lys->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=597]
-xref: record_id "597"
-xref: delta_mono_mass "-0.036386"
-xref: delta_avge_mass "-0.0431"
-xref: delta_composition "H(-4) C(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:21:32"
-xref: date_time_modified "2006-11-09 11:21:32"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:598
-name: Lys->Met
-def: "Lys->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=598]
-xref: record_id "598"
-xref: delta_mono_mass "2.945522"
-xref: delta_avge_mass "3.0238"
-xref: delta_composition "H(-3) C(-1) N(-1) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:21:56"
-xref: date_time_modified "2006-11-09 11:21:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:599
-name: Lys->Arg
-def: "Lys->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=599]
-xref: record_id "599"
-xref: delta_mono_mass "28.006148"
-xref: delta_avge_mass "28.0134"
-xref: delta_composition "N(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:22:15"
-xref: date_time_modified "2006-11-09 11:22:15"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:600
-name: Lys->Xle
-def: "Lys->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=600]
-xref: record_id "600"
-xref: delta_mono_mass "-15.010899"
-xref: delta_avge_mass "-15.0146"
-xref: delta_composition "H(-1) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:22:38"
-xref: date_time_modified "2011-06-21 15:25:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:601
-name: Xle->Ser
-def: "Leu/Ile->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=601]
-xref: record_id "601"
-xref: delta_mono_mass "-26.052036"
-xref: delta_avge_mass "-26.0803"
-xref: delta_composition "H(-6) C(-3) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:23:01"
-xref: date_time_modified "2011-06-21 15:29:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "I"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:602
-name: Xle->Phe
-def: "Leu/Ile->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=602]
-xref: record_id "602"
-xref: delta_mono_mass "33.98435"
-xref: delta_avge_mass "34.0162"
-xref: delta_composition "H(-2) C(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:23:22"
-xref: date_time_modified "2011-06-21 15:28:53"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "I"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:603
-name: Xle->Trp
-def: "Leu/Ile->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=603]
-xref: record_id "603"
-xref: delta_mono_mass "72.995249"
-xref: delta_avge_mass "73.0523"
-xref: delta_composition "H(-1) C(5) N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:23:48"
-xref: date_time_modified "2011-06-21 15:28:22"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "I"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:604
-name: Xle->Pro
-def: "Leu/Ile->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=604]
-xref: record_id "604"
-xref: delta_mono_mass "-16.0313"
-xref: delta_avge_mass "-16.0425"
-xref: delta_composition "H(-4) C(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:24:06"
-xref: date_time_modified "2011-06-21 15:29:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "I"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:605
-name: Xle->Val
-def: "Leu/Ile->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=605]
-xref: record_id "605"
-xref: delta_mono_mass "-14.01565"
-xref: delta_avge_mass "-14.0266"
-xref: delta_composition "H(-2) C(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:24:28"
-xref: date_time_modified "2011-06-21 15:28:33"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "I"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:606
-name: Xle->His
-def: "Leu/Ile->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=606]
-xref: record_id "606"
-xref: delta_mono_mass "23.974848"
-xref: delta_avge_mass "23.9816"
-xref: delta_composition "H(-4) N(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:24:50"
-xref: date_time_modified "2011-06-21 15:29:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "I"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:607
-name: Xle->Gln
-def: "Leu/Ile->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=607]
-xref: record_id "607"
-xref: delta_mono_mass "14.974514"
-xref: delta_avge_mass "14.9716"
-xref: delta_composition "H(-3) C(-1) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:25:14"
-xref: date_time_modified "2011-06-21 15:29:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "I"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:608
-name: Xle->Met
-def: "Leu/Ile->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=608]
-xref: record_id "608"
-xref: delta_mono_mass "17.956421"
-xref: delta_avge_mass "18.0384"
-xref: delta_composition "H(-2) C(-1) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:25:59"
-xref: date_time_modified "2011-06-21 15:28:43"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "I"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:609
-name: Xle->Arg
-def: "Leu/Ile->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=609]
-xref: record_id "609"
-xref: delta_mono_mass "43.017047"
-xref: delta_avge_mass "43.028"
-xref: delta_composition "H N(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:26:21"
-xref: date_time_modified "2011-06-21 15:28:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "I"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:610
-name: Met->Thr
-def: "Met->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=610]
-xref: record_id "610"
-xref: delta_mono_mass "-29.992806"
-xref: delta_avge_mass "-30.0922"
-xref: delta_composition "H(-2) C(-1) O S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:26:47"
-xref: date_time_modified "2006-11-09 11:26:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:611
-name: Met->Arg
-def: "Met->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=611]
-xref: record_id "611"
-xref: delta_mono_mass "25.060626"
-xref: delta_avge_mass "24.9896"
-xref: delta_composition "H(3) C N(3) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:27:10"
-xref: date_time_modified "2006-11-09 11:27:10"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:613
-name: Met->Lys
-def: "Met->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=613]
-xref: record_id "613"
-xref: delta_mono_mass "-2.945522"
-xref: delta_avge_mass "-3.0238"
-xref: delta_composition "H(3) C N S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:28:29"
-xref: date_time_modified "2006-11-09 11:28:29"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:614
-name: Met->Xle
-def: "Met->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=614]
-synonym: "Also Met->norleucine" RELATED []
-xref: record_id "614"
-xref: delta_mono_mass "-17.956421"
-xref: delta_avge_mass "-18.0384"
-xref: delta_composition "H(2) C S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:28:56"
-xref: date_time_modified "2018-02-28 16:07:26"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:615
-name: Met->Val
-def: "Met->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=615]
-xref: record_id "615"
-xref: delta_mono_mass "-31.972071"
-xref: delta_avge_mass "-32.065"
-xref: delta_composition "S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:29:27"
-xref: date_time_modified "2006-11-09 11:29:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:616
-name: Asn->Ser
-def: "Asn->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=616]
-xref: record_id "616"
-xref: delta_mono_mass "-27.010899"
-xref: delta_avge_mass "-27.0253"
-xref: delta_composition "H(-1) C(-1) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:29:57"
-xref: date_time_modified "2006-11-09 11:29:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:617
-name: Asn->Thr
-def: "Asn->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=617]
-xref: record_id "617"
-xref: delta_mono_mass "-12.995249"
-xref: delta_avge_mass "-12.9988"
-xref: delta_composition "H N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:34:11"
-xref: date_time_modified "2006-11-09 11:34:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:618
-name: Asn->Lys
-def: "Asn->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=618]
-xref: record_id "618"
-xref: delta_mono_mass "14.052036"
-xref: delta_avge_mass "14.0696"
-xref: delta_composition "H(6) C(2) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:34:31"
-xref: date_time_modified "2006-11-09 11:34:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:619
-name: Asn->Tyr
-def: "Asn->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=619]
-xref: record_id "619"
-xref: delta_mono_mass "49.020401"
-xref: delta_avge_mass "49.0706"
-xref: delta_composition "H(3) C(5) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:34:56"
-xref: date_time_modified "2006-11-09 11:34:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:620
-name: Asn->His
-def: "Asn->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=620]
-xref: record_id "620"
-xref: delta_mono_mass "23.015984"
-xref: delta_avge_mass "23.0366"
-xref: delta_composition "H C(2) N O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:35:18"
-xref: date_time_modified "2006-11-09 11:35:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:621
-name: Asn->Asp
-def: "Asn->Asp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=621]
-xref: record_id "621"
-xref: delta_mono_mass "0.984016"
-xref: delta_avge_mass "0.9848"
-xref: delta_composition "H(-1) N(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:35:42"
-xref: date_time_modified "2006-11-09 11:35:42"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:622
-name: Asn->Xle
-def: "Asn->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=622]
-xref: record_id "622"
-xref: delta_mono_mass "-0.958863"
-xref: delta_avge_mass "-0.945"
-xref: delta_composition "H(5) C(2) N(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:36:02"
-xref: date_time_modified "2011-06-21 15:13:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:623
-name: Pro->Ser
-def: "Pro->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=623]
-xref: record_id "623"
-xref: delta_mono_mass "-10.020735"
-xref: delta_avge_mass "-10.0379"
-xref: delta_composition "H(-2) C(-2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:36:26"
-xref: date_time_modified "2006-11-09 11:36:26"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:624
-name: Pro->Ala
-def: "Pro->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=624]
-xref: record_id "624"
-xref: delta_mono_mass "-26.01565"
-xref: delta_avge_mass "-26.0373"
-xref: delta_composition "H(-2) C(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:37:56"
-xref: date_time_modified "2006-11-09 11:37:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:625
-name: Pro->His
-def: "Pro->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=625]
-xref: record_id "625"
-xref: delta_mono_mass "40.006148"
-xref: delta_avge_mass "40.0241"
-xref: delta_composition "C N(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:38:18"
-xref: date_time_modified "2006-11-09 11:38:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:626
-name: Pro->Gln
-def: "Pro->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=626]
-xref: record_id "626"
-xref: delta_mono_mass "31.005814"
-xref: delta_avge_mass "31.014"
-xref: delta_composition "H N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:38:40"
-xref: date_time_modified "2006-11-09 11:38:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:627
-name: Pro->Thr
-def: "Pro->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=627]
-xref: record_id "627"
-xref: delta_mono_mass "3.994915"
-xref: delta_avge_mass "3.9887"
-xref: delta_composition "C(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:39:02"
-xref: date_time_modified "2006-11-09 11:39:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:628
-name: Pro->Arg
-def: "Pro->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=628]
-xref: record_id "628"
-xref: delta_mono_mass "59.048347"
-xref: delta_avge_mass "59.0705"
-xref: delta_composition "H(5) C N(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:39:29"
-xref: date_time_modified "2006-11-09 11:39:29"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:629
-name: Pro->Xle
-def: "Pro->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=629]
-xref: record_id "629"
-xref: delta_mono_mass "16.0313"
-xref: delta_avge_mass "16.0425"
-xref: delta_composition "H(4) C"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:39:47"
-xref: date_time_modified "2011-06-21 15:09:36"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:630
-name: Gln->Pro
-def: "Gln->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=630]
-xref: record_id "630"
-xref: delta_mono_mass "-31.005814"
-xref: delta_avge_mass "-31.014"
-xref: delta_composition "H(-1) N(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:40:19"
-xref: date_time_modified "2006-11-09 11:40:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:631
-name: Gln->Lys
-def: "Gln->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=631]
-xref: record_id "631"
-xref: delta_mono_mass "0.036386"
-xref: delta_avge_mass "0.0431"
-xref: delta_composition "H(4) C O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:42:17"
-xref: date_time_modified "2006-11-09 11:42:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:632
-name: Gln->Glu
-def: "Gln->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=632]
-xref: record_id "632"
-xref: delta_mono_mass "0.984016"
-xref: delta_avge_mass "0.9848"
-xref: delta_composition "H(-1) N(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:42:38"
-xref: date_time_modified "2006-11-09 11:42:38"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:633
-name: Gln->His
-def: "Gln->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=633]
-xref: record_id "633"
-xref: delta_mono_mass "9.000334"
-xref: delta_avge_mass "9.0101"
-xref: delta_composition "H(-1) C N O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:42:58"
-xref: date_time_modified "2006-11-09 11:42:58"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:634
-name: Gln->Arg
-def: "Gln->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=634]
-xref: record_id "634"
-xref: delta_mono_mass "28.042534"
-xref: delta_avge_mass "28.0565"
-xref: delta_composition "H(4) C N(2) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:43:25"
-xref: date_time_modified "2006-11-09 11:43:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:635
-name: Gln->Xle
-def: "Gln->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=635]
-xref: record_id "635"
-xref: delta_mono_mass "-14.974514"
-xref: delta_avge_mass "-14.9716"
-xref: delta_composition "H(3) C N(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:43:47"
-xref: date_time_modified "2011-06-21 15:09:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:636
-name: Arg->Ser
-def: "Arg->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=636]
-xref: record_id "636"
-xref: delta_mono_mass "-69.069083"
-xref: delta_avge_mass "-69.1084"
-xref: delta_composition "H(-7) C(-3) N(-3) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:44:13"
-xref: date_time_modified "2006-11-09 11:44:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:637
-name: Arg->Trp
-def: "Arg->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=637]
-xref: record_id "637"
-xref: delta_mono_mass "29.978202"
-xref: delta_avge_mass "30.0242"
-xref: delta_composition "H(-2) C(5) N(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:44:36"
-xref: date_time_modified "2006-11-09 11:44:36"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:638
-name: Arg->Thr
-def: "Arg->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=638]
-xref: record_id "638"
-xref: delta_mono_mass "-55.053433"
-xref: delta_avge_mass "-55.0818"
-xref: delta_composition "H(-5) C(-2) N(-3) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:44:59"
-xref: date_time_modified "2006-11-09 11:44:59"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:639
-name: Arg->Pro
-def: "Arg->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=639]
-xref: record_id "639"
-xref: delta_mono_mass "-59.048347"
-xref: delta_avge_mass "-59.0705"
-xref: delta_composition "H(-5) C(-1) N(-3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:45:18"
-xref: date_time_modified "2006-11-09 11:45:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:640
-name: Arg->Lys
-def: "Arg->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=640]
-xref: record_id "640"
-xref: delta_mono_mass "-28.006148"
-xref: delta_avge_mass "-28.0134"
-xref: delta_composition "N(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:45:37"
-xref: date_time_modified "2006-11-09 11:45:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:641
-name: Arg->His
-def: "Arg->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=641]
-xref: record_id "641"
-xref: delta_mono_mass "-19.042199"
-xref: delta_avge_mass "-19.0464"
-xref: delta_composition "H(-5) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:45:56"
-xref: date_time_modified "2006-11-09 11:45:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:642
-name: Arg->Gln
-def: "Arg->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=642]
-xref: record_id "642"
-xref: delta_mono_mass "-28.042534"
-xref: delta_avge_mass "-28.0565"
-xref: delta_composition "H(-4) C(-1) N(-2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:46:17"
-xref: date_time_modified "2006-11-09 11:46:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:643
-name: Arg->Met
-def: "Arg->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=643]
-xref: record_id "643"
-xref: delta_mono_mass "-25.060626"
-xref: delta_avge_mass "-24.9896"
-xref: delta_composition "H(-3) C(-1) N(-3) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:46:37"
-xref: date_time_modified "2006-11-09 11:46:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:644
-name: Arg->Cys
-def: "Arg->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=644]
-xref: record_id "644"
-xref: delta_mono_mass "-53.091927"
-xref: delta_avge_mass "-53.0428"
-xref: delta_composition "H(-7) C(-3) N(-3) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:47:00"
-xref: date_time_modified "2006-11-09 11:47:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:645
-name: Arg->Xle
-def: "Arg->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=645]
-xref: record_id "645"
-xref: delta_mono_mass "-43.017047"
-xref: delta_avge_mass "-43.028"
-xref: delta_composition "H(-1) N(-3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:47:36"
-xref: date_time_modified "2011-06-21 15:09:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:646
-name: Arg->Gly
-def: "Arg->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=646]
-xref: record_id "646"
-xref: delta_mono_mass "-99.079647"
-xref: delta_avge_mass "-99.1344"
-xref: delta_composition "H(-9) C(-4) N(-3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 11:48:00"
-xref: date_time_modified "2006-11-09 11:48:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:647
-name: Ser->Phe
-def: "Ser->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=647]
-xref: record_id "647"
-xref: delta_mono_mass "60.036386"
-xref: delta_avge_mass "60.0966"
-xref: delta_composition "H(4) C(6) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:32:55"
-xref: date_time_modified "2006-11-09 12:32:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:648
-name: Ser->Ala
-def: "Ser->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=648]
-xref: record_id "648"
-xref: delta_mono_mass "-15.994915"
-xref: delta_avge_mass "-15.9994"
-xref: delta_composition "O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:33:14"
-xref: date_time_modified "2006-11-09 12:33:14"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:649
-name: Ser->Trp
-def: "Ser->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=649]
-xref: record_id "649"
-xref: delta_mono_mass "99.047285"
-xref: delta_avge_mass "99.1326"
-xref: delta_composition "H(5) C(8) N O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:33:32"
-xref: date_time_modified "2006-11-09 12:33:32"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:650
-name: Ser->Thr
-def: "Ser->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=650]
-xref: record_id "650"
-xref: delta_mono_mass "14.01565"
-xref: delta_avge_mass "14.0266"
-xref: delta_composition "H(2) C"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:33:51"
-xref: date_time_modified "2006-11-09 12:33:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:651
-name: Ser->Asn
-def: "Ser->Asn substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=651]
-xref: record_id "651"
-xref: delta_mono_mass "27.010899"
-xref: delta_avge_mass "27.0253"
-xref: delta_composition "H C N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:34:12"
-xref: date_time_modified "2006-11-09 12:34:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:652
-name: Ser->Pro
-def: "Ser->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=652]
-xref: record_id "652"
-xref: delta_mono_mass "10.020735"
-xref: delta_avge_mass "10.0379"
-xref: delta_composition "H(2) C(2) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:34:34"
-xref: date_time_modified "2006-11-09 12:34:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:653
-name: Ser->Tyr
-def: "Ser->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=653]
-xref: record_id "653"
-xref: delta_mono_mass "76.0313"
-xref: delta_avge_mass "76.096"
-xref: delta_composition "H(4) C(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:35:00"
-xref: date_time_modified "2006-11-09 12:35:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:654
-name: Ser->Cys
-def: "Ser->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=654]
-xref: record_id "654"
-xref: delta_mono_mass "15.977156"
-xref: delta_avge_mass "16.0656"
-xref: delta_composition "O(-1) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:35:22"
-xref: date_time_modified "2006-11-09 12:35:22"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:655
-name: Ser->Arg
-def: "Ser->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=655]
-xref: record_id "655"
-xref: delta_mono_mass "69.069083"
-xref: delta_avge_mass "69.1084"
-xref: delta_composition "H(7) C(3) N(3) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:35:40"
-xref: date_time_modified "2006-11-09 12:35:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:656
-name: Ser->Xle
-def: "Ser->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=656]
-xref: record_id "656"
-xref: delta_mono_mass "26.052036"
-xref: delta_avge_mass "26.0803"
-xref: delta_composition "H(6) C(3) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:36:10"
-xref: date_time_modified "2011-06-21 15:08:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:657
-name: Ser->Gly
-def: "Ser->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=657]
-xref: record_id "657"
-xref: delta_mono_mass "-30.010565"
-xref: delta_avge_mass "-30.026"
-xref: delta_composition "H(-2) C(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:36:34"
-xref: date_time_modified "2006-11-09 12:36:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:658
-name: Thr->Ser
-def: "Thr->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=658]
-xref: record_id "658"
-xref: delta_mono_mass "-14.01565"
-xref: delta_avge_mass "-14.0266"
-xref: delta_composition "H(-2) C(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:36:57"
-xref: date_time_modified "2006-11-09 12:36:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:659
-name: Thr->Ala
-def: "Thr->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=659]
-xref: record_id "659"
-xref: delta_mono_mass "-30.010565"
-xref: delta_avge_mass "-30.026"
-xref: delta_composition "H(-2) C(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:37:15"
-xref: date_time_modified "2006-11-09 12:37:15"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:660
-name: Thr->Asn
-def: "Thr->Asn substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=660]
-xref: record_id "660"
-xref: delta_mono_mass "12.995249"
-xref: delta_avge_mass "12.9988"
-xref: delta_composition "H(-1) N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:37:37"
-xref: date_time_modified "2006-11-09 12:37:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:661
-name: Thr->Lys
-def: "Thr->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=661]
-xref: record_id "661"
-xref: delta_mono_mass "27.047285"
-xref: delta_avge_mass "27.0684"
-xref: delta_composition "H(5) C(2) N O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:37:55"
-xref: date_time_modified "2006-11-09 12:37:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:662
-name: Thr->Pro
-def: "Thr->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=662]
-xref: record_id "662"
-xref: delta_mono_mass "-3.994915"
-xref: delta_avge_mass "-3.9887"
-xref: delta_composition "C O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:38:14"
-xref: date_time_modified "2006-11-09 12:38:14"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:663
-name: Thr->Met
-def: "Thr->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=663]
-xref: record_id "663"
-xref: delta_mono_mass "29.992806"
-xref: delta_avge_mass "30.0922"
-xref: delta_composition "H(2) C O(-1) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:38:34"
-xref: date_time_modified "2006-11-09 12:38:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:664
-name: Thr->Xle
-def: "Thr->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=664]
-xref: record_id "664"
-xref: delta_mono_mass "12.036386"
-xref: delta_avge_mass "12.0538"
-xref: delta_composition "H(4) C(2) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:38:56"
-xref: date_time_modified "2011-06-21 15:25:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:665
-name: Thr->Arg
-def: "Thr->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=665]
-xref: record_id "665"
-xref: delta_mono_mass "55.053433"
-xref: delta_avge_mass "55.0818"
-xref: delta_composition "H(5) C(2) N(3) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:39:14"
-xref: date_time_modified "2006-11-09 12:39:14"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:666
-name: Val->Phe
-def: "Val->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=666]
-xref: record_id "666"
-xref: delta_mono_mass "48"
-xref: delta_avge_mass "48.0428"
-xref: delta_composition "C(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:39:35"
-xref: date_time_modified "2006-11-09 12:39:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:667
-name: Val->Ala
-def: "Val->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=667]
-xref: record_id "667"
-xref: delta_mono_mass "-28.0313"
-xref: delta_avge_mass "-28.0532"
-xref: delta_composition "H(-4) C(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:40:00"
-xref: date_time_modified "2006-11-09 12:40:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:668
-name: Val->Glu
-def: "Val->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=668]
-xref: record_id "668"
-xref: delta_mono_mass "29.974179"
-xref: delta_avge_mass "29.9829"
-xref: delta_composition "H(-2) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:40:19"
-xref: date_time_modified "2006-11-09 12:40:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:669
-name: Val->Met
-def: "Val->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=669]
-xref: record_id "669"
-xref: delta_mono_mass "31.972071"
-xref: delta_avge_mass "32.065"
-xref: delta_composition "S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:40:36"
-xref: date_time_modified "2006-11-09 12:40:36"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:670
-name: Val->Asp
-def: "Val->Asp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=670]
-xref: record_id "670"
-xref: delta_mono_mass "15.958529"
-xref: delta_avge_mass "15.9563"
-xref: delta_composition "H(-4) C(-1) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:41:04"
-xref: date_time_modified "2006-11-09 12:41:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:671
-name: Val->Xle
-def: "Val->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=671]
-xref: record_id "671"
-xref: delta_mono_mass "14.01565"
-xref: delta_avge_mass "14.0266"
-xref: delta_composition "H(2) C"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:41:27"
-xref: date_time_modified "2011-06-21 15:08:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:672
-name: Val->Gly
-def: "Val->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=672]
-xref: record_id "672"
-xref: delta_mono_mass "-42.04695"
-xref: delta_avge_mass "-42.0797"
-xref: delta_composition "H(-6) C(-3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:41:45"
-xref: date_time_modified "2006-11-09 12:41:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:673
-name: Trp->Ser
-def: "Trp->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=673]
-xref: record_id "673"
-xref: delta_mono_mass "-99.047285"
-xref: delta_avge_mass "-99.1326"
-xref: delta_composition "H(-5) C(-8) N(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:42:22"
-xref: date_time_modified "2006-11-09 12:42:22"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:674
-name: Trp->Cys
-def: "Trp->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=674]
-xref: record_id "674"
-xref: delta_mono_mass "-83.070128"
-xref: delta_avge_mass "-83.067"
-xref: delta_composition "H(-5) C(-8) N(-1) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:42:46"
-xref: date_time_modified "2006-11-09 12:42:46"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:675
-name: Trp->Arg
-def: "Trp->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=675]
-xref: record_id "675"
-xref: delta_mono_mass "-29.978202"
-xref: delta_avge_mass "-30.0242"
-xref: delta_composition "H(2) C(-5) N(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:43:10"
-xref: date_time_modified "2006-11-09 12:43:10"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:676
-name: Trp->Gly
-def: "Trp->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=676]
-xref: record_id "676"
-xref: delta_mono_mass "-129.057849"
-xref: delta_avge_mass "-129.1586"
-xref: delta_composition "H(-7) C(-9) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:43:29"
-xref: date_time_modified "2006-11-09 12:43:29"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:677
-name: Trp->Xle
-def: "Trp->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=677]
-xref: record_id "677"
-xref: delta_mono_mass "-72.995249"
-xref: delta_avge_mass "-73.0523"
-xref: delta_composition "H C(-5) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:43:49"
-xref: date_time_modified "2011-06-21 15:08:09"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:678
-name: Tyr->Phe
-def: "Tyr->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=678]
-xref: record_id "678"
-xref: delta_mono_mass "-15.994915"
-xref: delta_avge_mass "-15.9994"
-xref: delta_composition "O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:44:13"
-xref: date_time_modified "2006-11-09 12:44:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:679
-name: Tyr->Ser
-def: "Tyr->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=679]
-xref: record_id "679"
-xref: delta_mono_mass "-76.0313"
-xref: delta_avge_mass "-76.096"
-xref: delta_composition "H(-4) C(-6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:44:37"
-xref: date_time_modified "2006-11-09 12:44:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:680
-name: Tyr->Asn
-def: "Tyr->Asn substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=680]
-xref: record_id "680"
-xref: delta_mono_mass "-49.020401"
-xref: delta_avge_mass "-49.0706"
-xref: delta_composition "H(-3) C(-5) N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:44:59"
-xref: date_time_modified "2006-11-09 12:44:59"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:681
-name: Tyr->His
-def: "Tyr->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=681]
-xref: record_id "681"
-xref: delta_mono_mass "-26.004417"
-xref: delta_avge_mass "-26.034"
-xref: delta_composition "H(-2) C(-3) N(2) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:45:22"
-xref: date_time_modified "2006-11-09 12:45:22"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:682
-name: Tyr->Asp
-def: "Tyr->Asp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=682]
-xref: record_id "682"
-xref: delta_mono_mass "-48.036386"
-xref: delta_avge_mass "-48.0859"
-xref: delta_composition "H(-4) C(-5) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:45:44"
-xref: date_time_modified "2006-11-09 12:45:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:683
-name: Tyr->Cys
-def: "Tyr->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=683]
-xref: record_id "683"
-xref: delta_mono_mass "-60.054144"
-xref: delta_avge_mass "-60.0304"
-xref: delta_composition "H(-4) C(-6) O(-1) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-09 12:46:03"
-xref: date_time_modified "2006-11-09 12:46:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:684
-name: BDMAPP
-def: "Mass Defect Tag on lysine e-amino." [URL:http\://www.targetdiscovery.com/article.php?topic=crpc.prst&story=20060321132643690, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=684]
-xref: record_id "684"
-xref: delta_mono_mass "253.010225"
-xref: delta_avge_mass "254.1231"
-xref: delta_composition "H(12) C(11) N O Br"
-xref: username_of_poster "LVSchneid"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-13 18:51:11"
-xref: date_time_modified "2006-11-13 18:52:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_misc_notes "Low efficiency"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "Y"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Artefact"
-xref: spec_4_misc_notes "Low efficiency"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "W"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Artefact"
-xref: spec_5_misc_notes "Low efficiency"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:685
-name: NA-LNO2
-def: "Nitroalkylation by Nitro Linoleic Acid." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=685]
-comment: Reversible post-translational modification of proteins by nitrated fatty acids.
-synonym: "Michael addition of nitro-linoleic acid to Cys and His" RELATED []
-xref: record_id "685"
-xref: delta_mono_mass "325.225309"
-xref: delta_avge_mass "325.443"
-xref: delta_composition "H(31) C(18) N O(4)"
-xref: username_of_poster "cbatthya"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-13 18:59:35"
-xref: date_time_modified "2006-11-13 18:59:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:686
-name: NA-OA-NO2
-def: "Nitroalkylation by Nitro Oleic Acid." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=686]
-comment: Reversible post-translational modification of proteins by nitrated fatty acids.
-synonym: "Michael addition of nitro-oleic acid to Cys and His" RELATED []
-xref: record_id "686"
-xref: delta_mono_mass "327.240959"
-xref: delta_avge_mass "327.4589"
-xref: delta_composition "H(33) C(18) N O(4)"
-xref: username_of_poster "cbatthya"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-13 19:01:33"
-xref: date_time_modified "2006-11-13 19:01:33"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:687
-name: ICPL:2H(4)
-def: "Bruker Daltonics SERVA-ICPL(TM) quantification chemistry, medium form." [URL:http\://www.bdal.de/life-science-tools/care-consumables-more/icpl-kit.html, PMID:15602776, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=687]
-comment: Attention: As the digest is typically applied AFTER ICPL_light/heavy labeling, only ProteinN-term labeling and Lys-specific labeling is applied.
-xref: record_id "687"
-xref: delta_mono_mass "109.046571"
-xref: delta_avge_mass "109.1188"
-xref: delta_composition "H(-1) 2H(4) C(6) N O"
-xref: username_of_poster "suckau"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-13 19:05:12"
-xref: date_time_modified "2008-09-03 15:26:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_2_misc_notes "Use when labelling pre-digest"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Use when labelling post-digest"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:695
-name: Label:13C(6)15N(1)
-def: "13C(6) 15N(1) Silac label." [URL:http\://www.pil.sdu.dk/silac_intro.htm, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=695]
-xref: record_id "695"
-xref: delta_mono_mass "7.017164"
-xref: delta_avge_mass "6.9493"
-xref: delta_composition "C(-6) 13C(6) N(-1) 15N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2006-11-29 15:10:53"
-xref: date_time_modified "2007-08-22 18:30:49"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "I"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:696
-name: Label:2H(9)13C(6)15N(2)
-def: "13C(6) 15N(2) (D)9 SILAC label." [URL:http\://www.pil.sdu.dk/silac_intro.htm, URL:http\://www.isotope.com/cil/products/displayproduct.cfm?prod_id=8635, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=696]
-synonym: "heavy D9 lysine" RELATED []
-xref: record_id "696"
-xref: delta_mono_mass "17.07069"
-xref: delta_avge_mass "16.9982"
-xref: delta_composition "H(-9) 2H(9) C(-6) 13C(6) N(-2) 15N(2)"
-xref: username_of_poster "striker2000"
-xref: group_of_poster ""
-xref: date_time_posted "2006-12-01 22:36:25"
-xref: date_time_modified "2007-08-22 18:48:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "Used in SILAC experiment"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:697
-name: NIC
-def: "Nicotinic Acid." [PMID:15004565, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=697]
-xref: record_id "697"
-xref: delta_mono_mass "105.021464"
-xref: delta_avge_mass "105.0941"
-xref: delta_composition "H(3) C(6) N O"
-xref: username_of_poster "verena-meyer"
-xref: group_of_poster ""
-xref: date_time_posted "2006-12-04 16:04:56"
-xref: date_time_modified "2024-08-12 10:05:07"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:698
-name: dNIC
-def: "Deuterated Nicotinic Acid." [PMID:15004565, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=698]
-xref: record_id "698"
-xref: delta_mono_mass "109.048119"
-xref: delta_avge_mass "109.1205"
-xref: delta_composition "H 2H(3) C(6) N O"
-xref: username_of_poster "verena-meyer"
-xref: group_of_poster ""
-xref: date_time_posted "2006-12-04 16:12:54"
-xref: date_time_modified "2024-08-12 10:04:46"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:720
-name: HNE-Delta:H(2)O
-def: "Dehydrated 4-hydroxynonenal." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=720]
-comment: Mass Spectroscopic Characterization of Protein Modification by 4-Hydroxy-2-(E)-nonenal and 4-Oxo-2-(E)-nonenal.
-xref: record_id "720"
-xref: delta_mono_mass "138.104465"
-xref: delta_avge_mass "138.2069"
-xref: delta_composition "H(14) C(9) O"
-xref: username_of_poster "stewartb"
-xref: group_of_poster ""
-xref: date_time_posted "2007-01-08 18:29:46"
-xref: date_time_modified "2007-01-21 18:27:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:721
-name: 4-ONE
-def: "4-Oxononenal (ONE)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=721]
-comment: Covalent adduction of nucleophilic amino acids by 4-hydroxynonenal and 4-oxononenal.
-xref: record_id "721"
-xref: delta_mono_mass "154.09938"
-xref: delta_avge_mass "154.2063"
-xref: delta_composition "H(14) C(9) O(2)"
-xref: username_of_poster "stewartb"
-xref: group_of_poster ""
-xref: date_time_posted "2007-01-08 19:41:28"
-xref: date_time_modified "2007-01-21 18:26:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:723
-name: O-Dimethylphosphate
-def: "O-Dimethylphosphorylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=723]
-xref: record_id "723"
-xref: delta_mono_mass "107.997631"
-xref: delta_avge_mass "108.0331"
-xref: delta_composition "H(5) C(2) O(3) P"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2007-01-09 21:25:28"
-xref: date_time_modified "2007-01-13 21:01:15"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:724
-name: O-Methylphosphate
-def: "O-Methylphosphorylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=724]
-comment: Created by auto-catalytic dealkylation of the O-Dimethylphosphate adduct.
-xref: record_id "724"
-xref: delta_mono_mass "93.981981"
-xref: delta_avge_mass "94.0065"
-xref: delta_composition "H(3) C O(3) P"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2007-01-09 21:35:38"
-xref: date_time_modified "2007-01-21 18:13:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:725
-name: Diethylphosphate
-def: "O-Diethylphosphorylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=725]
-xref: record_id "725"
-xref: delta_mono_mass "136.028931"
-xref: delta_avge_mass "136.0862"
-xref: delta_composition "H(9) C(4) O(3) P"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2007-01-09 21:44:04"
-xref: date_time_modified "2011-12-05 16:15:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "K"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "C"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "H"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "N-term"
-xref: spec_7_position "Any N-term"
-xref: spec_7_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:726
-name: Ethylphosphate
-def: "O-Ethylphosphorylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=726]
-comment: Created by auto-catalytic dealkylation of the O-Diethylphosphate adduct.
-xref: record_id "726"
-xref: delta_mono_mass "107.997631"
-xref: delta_avge_mass "108.0331"
-xref: delta_composition "H(5) C(2) O(3) P"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2007-01-09 21:46:17"
-xref: date_time_modified "2011-12-05 16:15:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "K"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "N-term"
-xref: spec_5_position "Any N-term"
-xref: spec_5_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:727
-name: O-pinacolylmethylphosphonate
-def: "O-pinacolylmethylphosphonylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=727]
-xref: record_id "727"
-xref: delta_mono_mass "162.080967"
-xref: delta_avge_mass "162.1666"
-xref: delta_composition "H(15) C(7) O(2) P"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2007-01-10 16:04:46"
-xref: date_time_modified "2010-04-29 08:38:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "H"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "K"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:728
-name: Methylphosphonate
-def: "Methylphosphonylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=728]
-comment: Created by auto-catalytic dealkylation of either the O-pinacolylmethylphosphonate adduct, or the O-isopropylmethylphosphonate adduct.
-xref: record_id "728"
-xref: delta_mono_mass "77.987066"
-xref: delta_avge_mass "78.0071"
-xref: delta_composition "H(3) C O(2) P"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2007-01-10 16:07:37"
-xref: date_time_modified "2007-01-21 18:11:36"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:729
-name: O-Isopropylmethylphosphonate
-def: "O-Isopropylmethylphosphonylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=729]
-xref: record_id "729"
-xref: delta_mono_mass "120.034017"
-xref: delta_avge_mass "120.0868"
-xref: delta_composition "H(9) C(4) O(2) P"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2007-01-10 16:10:55"
-xref: date_time_modified "2007-01-13 21:02:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:730
-name: iTRAQ8plex
-def: "Representative mass and accurate mass for 113, 114, 116 & 117." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=730]
-comment: Other 4 channels have the same nominal mass but slightly different exact mass. For quantitation purposes, use this entry for all channels.
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry AKA iTRAQ8plex:13C(7)15N(1)" RELATED []
-xref: record_id "730"
-xref: delta_mono_mass "304.20536"
-xref: delta_avge_mass "304.3074"
-xref: delta_composition "H(24) C(7) 13C(7) N(3) 15N O(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2007-01-11 09:53:13"
-xref: date_time_modified "2024-08-12 09:56:06"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "0"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Low abundance"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "H"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "Very low abundance"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "S"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Isotopic label"
-xref: spec_5_misc_notes "Very low abundance"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "T"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Isotopic label"
-xref: spec_6_misc_notes "Very low abundance"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "N-term"
-xref: spec_7_position "Protein N-term"
-xref: spec_7_classification "Isotopic label"
-xref: spec_8_group "8"
-xref: spec_8_hidden "1"
-xref: spec_8_site "C"
-xref: spec_8_position "Anywhere"
-xref: spec_8_classification "Isotopic label"
-xref: spec_8_misc_notes "side reaction"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:731
-name: iTRAQ8plex:13C(6)15N(2)
-def: "Accurate mass for 115, 118, 119 & 121." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=731]
-comment: Other 4 channels have the same nominal mass but slightly different exact mass. For quantitation purposes, use iTRAQ8plex for all channels.
-synonym: "Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry" RELATED []
-xref: record_id "731"
-xref: delta_mono_mass "304.19904"
-xref: delta_avge_mass "304.3081"
-xref: delta_composition "H(24) C(8) 13C(6) N(2) 15N(2) O(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2007-01-11 09:56:21"
-xref: date_time_modified "2024-08-12 09:56:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Low abundance"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "C"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "side reaction"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:734
-name: Ethanolamine
-def: "Carboxyl modification with ethanolamine." [PMID:2, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=734]
-comment: Carbodiimide mediated blocking of free carboxylic acids (Asp/Glu sidechains and C-termini) with ethanolamine; reaction yields an amide-bond between the carboxylic acid of the peptide/protein and the primary amine of ethanolamine; reaction irreversibly modifies carboxylic acids. Shown above is the composition of the mass adduct, after substraction of water.
-xref: record_id "734"
-xref: delta_mono_mass "43.042199"
-xref: delta_avge_mass "43.0678"
-xref: delta_composition "H(5) C(2) N"
-xref: username_of_poster "overalllab"
-xref: group_of_poster ""
-xref: date_time_posted "2007-01-31 22:04:44"
-xref: date_time_modified "2012-11-01 12:02:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Any C-term"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "D"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "E"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "C"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:735
-name: BEMAD_ST
-def: "Beta elimination of modified S or T followed by Michael addition of DTT." [PMID:15648052, PMID:17116471, PMID:12438562, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=735]
-comment: Beta-elimination and Michael addition of dithiothreitol (DTT) to serine and threonine adds a weight of approximately 136.2.
-synonym: "threo-1,4-dimercaptobutane-2,3-diol Was DTT_ST" RELATED []
-xref: record_id "735"
-xref: delta_mono_mass "136.001656"
-xref: delta_avge_mass "136.2357"
-xref: delta_composition "H(8) C(4) O S(2)"
-xref: username_of_poster "stephenaw777"
-xref: group_of_poster ""
-xref: date_time_posted "2007-02-10 00:00:43"
-xref: date_time_modified "2017-06-15 14:01:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "The addition of DTT adds 136.2 not 154.2 to Serine due to loss of water in reaction"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_2_misc_notes "The addition of DTT adds 136.2 not 154.2 to Threonine due to loss of water in reaction"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:736
-name: BEMAD_C
-def: "Beta elimination of alkylated Cys followed by Michael addition of DTT." [PMID:12438562, PMID:17116471, PMID:16452088, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=736]
-comment: When the beta-elimination and Michael addition of dithiothreitol (DTT) (BEMAD) reaction is used with alkylated cysteine a sulfur group is lost leaving the addition of approximately 120.2 in the chemical reaction.
-synonym: "Was DTT_C" RELATED []
-xref: record_id "736"
-xref: delta_mono_mass "120.0245"
-xref: delta_avge_mass "120.1701"
-xref: delta_composition "H(8) C(4) O(2) S"
-xref: username_of_poster "stephenaw777"
-xref: group_of_poster ""
-xref: date_time_posted "2007-02-10 03:12:41"
-xref: date_time_modified "2017-06-15 13:58:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:737
-name: TMT6plex
-def: "Sixplex Tandem Mass Tag®." [URL:http\://www.piercenet.com/instructions/2162457.pdf, URL:https\://www.piercenet.com/instructions/2162073.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=737]
-comment: M/z values of the TMT® fragment ions to be quantified for 6plex and 10plex: 126.12773 127.12476 128.13443 129.13147 130.14114 131.13818. Additional m/z values for 10plex: 127.13108 128.12811 129.13779 130.13482.
-synonym: "Tandem Mass Tag sixplex labelling kit Proteome Sciences Also applies to TMT10plex Tandem Mass Tag® and TMT® are registered Trademarks of Proteome Sciences plc. This is a nominal. representative mass" RELATED []
-xref: record_id "737"
-xref: delta_mono_mass "229.162932"
-xref: delta_avge_mass "229.2634"
-xref: delta_composition "H(20) C(8) 13C(4) N 15N O(2)"
-xref: username_of_poster "JUergen.schaefer"
-xref: group_of_poster ""
-xref: date_time_posted "2007-03-01 13:44:23"
-xref: date_time_modified "2024-08-12 10:10:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Isotopic label"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "H"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "S"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Isotopic label"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "T"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:738
-name: TMT2plex
-def: "Duplex Tandem Mass Tag®." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=738]
-comment: Duplex-TMT® reagents 2TMT-126, 2TMT-127. m/z values of the TMT® fragment ions to be quantified: 126.12773 127.13108.
-synonym: "Tandem Mass Tag Duplex labelling kit Proteome Sciences Tandem Mass Tag® and TMT® are registered Trademarks of Proteome Sciences plc." RELATED []
-xref: record_id "738"
-xref: delta_mono_mass "225.155833"
-xref: delta_avge_mass "225.2921"
-xref: delta_composition "H(20) C(11) 13C N(2) O(2)"
-xref: username_of_poster "JUergen.schaefer"
-xref: group_of_poster ""
-xref: date_time_posted "2007-03-01 13:53:36"
-xref: date_time_modified "2024-08-12 10:09:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Isotopic label"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "H"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "S"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Isotopic label"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "T"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:739
-name: TMT
-def: "Native Tandem Mass Tag®." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=739]
-comment: This modification describes the \"native\" TMT Reagent without isotopic label.
-synonym: "Tandem Mass Tag® and TMT® are registered Trademarks of Proteome Sciences plc." RELATED []
-xref: record_id "739"
-xref: delta_mono_mass "224.152478"
-xref: delta_avge_mass "224.2994"
-xref: delta_composition "H(20) C(12) N(2) O(2)"
-xref: username_of_poster "JUergen.schaefer"
-xref: group_of_poster ""
-xref: date_time_posted "2007-03-02 09:29:50"
-xref: date_time_modified "2024-08-12 10:08:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "H"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "S"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Isotopic label"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "T"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:740
-name: ExacTagThiol
-def: "ExacTag Thiol label mass for 2-4-7-10 plex." [URL:http\://www.perkinelmer.com/exactag, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=740]
-comment: Accurate mass for Exactag Thiol labels.
-synonym: "PerkinElmer ExacTag Thiol kit" RELATED []
-xref: record_id "740"
-xref: delta_mono_mass "972.365219"
-xref: delta_avge_mass "972.7268"
-xref: delta_composition "H(50) C(23) 13C(12) N(8) 15N(6) O(18)"
-xref: username_of_poster "cparman"
-xref: group_of_poster ""
-xref: date_time_posted "2007-03-02 17:24:48"
-xref: date_time_modified "2017-10-09 15:48:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:741
-name: ExacTagAmine
-def: "ExacTag Amine label mass for 2-4-7-10 plex." [URL:http\://www.perkinelmer.com/exactag, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=741]
-comment: Accurate mass for Exactag Amine labels. Includes the mass of the conjugation reagent.
-synonym: "PerkinElmer ExacTag Amine kit" RELATED []
-xref: record_id "741"
-xref: delta_mono_mass "1046.347854"
-xref: delta_avge_mass "1046.8285"
-xref: delta_composition "H(52) C(25) 13C(12) N(8) 15N(6) O(19) S"
-xref: username_of_poster "cparman"
-xref: group_of_poster ""
-xref: date_time_posted "2007-03-02 17:28:02"
-xref: date_time_modified "2017-10-09 15:48:14"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:743
-name: 4-ONE+Delta:H(-2)O(-1)
-def: "Dehydrated 4-Oxononenal Michael adduct." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=743]
-comment: Mass Spectorscopic Characterization of Protein Modification by 4-hydroxy-2-(E)-nonenal and 4-oxo-2-(E)-nonenal.
-xref: record_id "743"
-xref: delta_mono_mass "136.088815"
-xref: delta_avge_mass "136.191"
-xref: delta_composition "H(12) C(9) O"
-xref: username_of_poster "stewartb"
-xref: group_of_poster ""
-xref: date_time_posted "2007-03-21 21:21:34"
-xref: date_time_modified "2007-04-08 18:56:36"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:744
-name: NO_SMX_SEMD
-def: "Nitroso Sulfamethoxazole Sulphenamide thiol adduct." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=744]
-comment: Synthesis and Reactions of Nitroso Sulphamethoxazole with Biological Nucleophiles: Implications for Immune Mediated Toxicity.
-xref: record_id "744"
-xref: delta_mono_mass "251.036462"
-xref: delta_avge_mass "251.2618"
-xref: delta_composition "H(9) C(10) N(3) O(3) S"
-xref: username_of_poster "stewartb"
-xref: group_of_poster ""
-xref: date_time_posted "2007-04-17 23:28:29"
-xref: date_time_modified "2021-07-06 12:30:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:746
-name: NO_SMX_SIMD
-def: "Nitroso Sulfamethoxazole Sulfinamide thiol adduct." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=746]
-comment: Synthesis and Reactions of Nitroso Sulphamethoxazole with Biological Nucleophiles: Implications for Immune Mediated Toxicity.
-xref: record_id "746"
-xref: delta_mono_mass "267.031377"
-xref: delta_avge_mass "267.2612"
-xref: delta_composition "H(9) C(10) N(3) O(4) S"
-xref: username_of_poster "stewartb"
-xref: group_of_poster ""
-xref: date_time_posted "2007-04-18 21:39:11"
-xref: date_time_modified "2007-04-21 16:56:07"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:747
-name: Malonyl
-def: "Malonylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=747]
-xref: record_id "747"
-xref: delta_mono_mass "86.000394"
-xref: delta_avge_mass "86.0462"
-xref: delta_composition "H(2) C(3) O(3)"
-xref: username_of_poster "massy"
-xref: group_of_poster ""
-xref: date_time_posted "2007-05-17 14:17:42"
-xref: date_time_modified "2024-06-27 10:17:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-xref: spec_3_neutral_loss_44_mono_mass "43.989829"
-xref: spec_3_neutral_loss_44_avge_mass "44.0095"
-xref: spec_3_neutral_loss_44_flag "false"
-xref: spec_3_neutral_loss_44_composition "C O(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:748
-name: 3sulfo
-def: "Derivatization by N-term modification using 3-Sulfobenzoic succinimidyl ester." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=748]
-xref: record_id "748"
-xref: delta_mono_mass "183.983029"
-xref: delta_avge_mass "184.1693"
-xref: delta_composition "H(4) C(7) O(4) S"
-xref: username_of_poster "MaxWis"
-xref: group_of_poster ""
-xref: date_time_posted "2007-05-31 10:15:48"
-xref: date_time_modified "2007-06-24 19:58:07"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:750
-name: trifluoro
-def: "Trifluoroleucine replacement of leucine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=750]
-xref: record_id "750"
-xref: delta_mono_mass "53.971735"
-xref: delta_avge_mass "53.9714"
-xref: delta_composition "H(-3) F(3)"
-xref: username_of_poster "UKMSF"
-xref: group_of_poster ""
-xref: date_time_posted "2007-06-13 17:10:33"
-xref: date_time_modified "2007-06-24 19:56:32"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Non-standard residue"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:751
-name: TNBS
-def: "Tri nitro benzene." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=751]
-xref: record_id "751"
-xref: delta_mono_mass "210.986535"
-xref: delta_avge_mass "211.0886"
-xref: delta_composition "H C(6) N(3) O(6)"
-xref: username_of_poster "DelphineP"
-xref: group_of_poster ""
-xref: date_time_posted "2007-06-21 13:36:03"
-xref: date_time_modified "2007-06-24 19:58:58"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:762
-name: IDEnT
-def: "Isotope Distribution Encoded Tag." [PMID:10740847, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=762]
-comment: Modified peptides identified by isotope pattern. Restriction to cysteine-containing peptides combined with high mass accuracy allows peptide identification.
-synonym: "2,4-dichlorobenzylcarbamidomethyl" RELATED []
-xref: record_id "762"
-xref: delta_mono_mass "214.990469"
-xref: delta_avge_mass "216.064"
-xref: delta_composition "H(7) C(9) N O Cl(2)"
-xref: username_of_poster "chalkley"
-xref: group_of_poster ""
-xref: date_time_posted "2007-07-10 20:14:50"
-xref: date_time_modified "2007-07-15 20:04:29"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:763
-name: BEMAD_ST:2H(6)
-def: "Beta elimination of modified S or T followed by Michael addition of labelled DTT." [PMID:15648052, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=763]
-comment: Can be used for quantitative analysis of O-linked post-translational modifications. Same reaction can be used for quantitative analysis of cysteine-containing peptides, but then the modification is 16 Da less in mass; i.e. isotopically labeled reagent adds 126 Da in mass.
-synonym: "Was DTT_ST:2H(6)" RELATED []
-xref: record_id "763"
-xref: delta_mono_mass "142.039317"
-xref: delta_avge_mass "142.2727"
-xref: delta_composition "H(2) 2H(6) C(4) O S(2)"
-xref: username_of_poster "chalkley"
-xref: group_of_poster ""
-xref: date_time_posted "2007-07-10 20:34:46"
-xref: date_time_modified "2017-06-15 14:01:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:764
-name: BEMAD_C:2H(6)
-def: "Beta elimination of alkylated Cys followed by Michael addition of labelled DTT." [PMID:15648052, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=764]
-comment: Can be used for quantitative analysis of cysteine-containing peptides. Same reaction can be used for quantitative analysis of O-linked post-translational modifications to serines and threonines, but then the modification is 16 Da more in mass; i.e. isotopically labeled reagent adds 142 Da in mass.
-synonym: "Was DTT_C:2H(6) Isotopically labeled Dithiothreitol (DTT) modification of cysteines" RELATED []
-xref: record_id "764"
-xref: delta_mono_mass "126.062161"
-xref: delta_avge_mass "126.2071"
-xref: delta_composition "H(2) 2H(6) C(4) O(2) S"
-xref: username_of_poster "chalkley"
-xref: group_of_poster ""
-xref: date_time_posted "2007-07-10 20:44:56"
-xref: date_time_modified "2017-06-15 13:59:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:765
-name: Met-loss
-def: "Removal of initiator methionine from protein N-terminus." [PMID:3327521, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=765]
-comment: N-terminal initiator methionine is removed by a methionine aminopeptidase from proteins where the residue following the methionine is Ala, Cys, Gly, Pro, Ser, Thr or Val. This is generally the final N-terminal state for proteins where the following residue was a Cys, Pro or Val.
-xref: record_id "765"
-xref: delta_mono_mass "-131.040485"
-xref: delta_avge_mass "-131.1961"
-xref: delta_composition "H(-9) C(-5) N(-1) O(-1) S(-1)"
-xref: username_of_poster "chalkley"
-xref: group_of_poster ""
-xref: date_time_posted "2007-07-10 22:40:00"
-xref: date_time_modified "2007-07-15 20:01:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Protein N-term"
-xref: spec_1_classification "Co-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:766
-name: Met-loss+Acetyl
-def: "Removal of initiator methionine from protein N-terminus, then acetylation of the new N-terminus." [PMID:3327521, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=766]
-comment: The N-terminal initiator methionine is removed by a methionine aminopeptidase from proteins whose residue following the methionine is Ala, Cys, Gly, Pro, Ser, Thr or Val. Proteins whose following residue was Ala, Gly, Ser or Thr are then acetylated by an N(alpha)-acetyltransferase on the new N-terminus.
-xref: record_id "766"
-xref: delta_mono_mass "-89.02992"
-xref: delta_avge_mass "-89.1594"
-xref: delta_composition "H(-7) C(-3) N(-1) S(-1)"
-xref: username_of_poster "chalkley"
-xref: group_of_poster ""
-xref: date_time_posted "2007-07-10 22:57:12"
-xref: date_time_modified "2007-07-15 20:01:06"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Protein N-term"
-xref: spec_1_classification "Co-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:767
-name: Menadione-HQ
-def: "Menadione hydroquinone derivative." [PMID:15939799, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=767]
-xref: record_id "767"
-xref: delta_mono_mass "172.05243"
-xref: delta_avge_mass "172.18"
-xref: delta_composition "H(8) C(11) O(2)"
-xref: username_of_poster "catsriku"
-xref: group_of_poster ""
-xref: date_time_posted "2007-07-12 07:35:07"
-xref: date_time_modified "2007-07-15 20:05:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:768
-name: Methyl+Acetyl:2H(3)
-def: "Mono-methylated lysine labelled with Acetyl_heavy." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=768]
-xref: record_id "768"
-xref: delta_mono_mass "59.045045"
-xref: delta_avge_mass "59.0817"
-xref: delta_composition "H 2H(3) C(3) O"
-xref: username_of_poster "buchanan"
-xref: group_of_poster ""
-xref: date_time_posted "2007-08-06 09:35:40"
-xref: date_time_modified "2007-09-07 16:56:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:771
-name: lapachenole
-def: "Lapachenole photochemically added to cysteine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=771]
-xref: record_id "771"
-xref: delta_mono_mass "240.11503"
-xref: delta_avge_mass "240.297"
-xref: delta_composition "H(16) C(16) O(2)"
-xref: username_of_poster "hmfales"
-xref: group_of_poster ""
-xref: date_time_posted "2007-08-17 22:22:15"
-xref: date_time_modified "2007-09-07 16:52:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "Simple cyclic compound C16H16O2 adds to cysteine forming fluorescent derivative."
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:772
-name: Label:13C(5)
-def: "13C(5) Silac label." [URL:http\://www.pil.sdu.dk/silac_intro.htm, PMID:12716131, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=772]
-xref: record_id "772"
-xref: delta_mono_mass "5.016774"
-xref: delta_avge_mass "4.9633"
-xref: delta_composition "C(-5) 13C(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2007-08-22 18:36:11"
-xref: date_time_modified "2007-08-22 18:36:11"
-xref: approved "1"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "Result of Arg to Pro conversion of 13C(6) labelled Arg"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:773
-name: maleimide
-def: "Maleimide." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=773]
-xref: record_id "773"
-xref: delta_mono_mass "97.016378"
-xref: delta_avge_mass "97.0721"
-xref: delta_composition "H(3) C(4) N O(2)"
-xref: username_of_poster "mjayson"
-xref: group_of_poster ""
-xref: date_time_posted "2007-09-05 23:31:52"
-xref: date_time_modified "2007-09-06 11:28:09"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:774
-name: Biotin-phenacyl
-def: "Alkylation by biotinylated form of phenacyl bromide." [PMID:428399, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=774]
-comment: Phenacyl bromide conjugated with a linker and biotin tag, details not published yet.
-xref: record_id "774"
-xref: delta_mono_mass "626.263502"
-xref: delta_avge_mass "626.727"
-xref: delta_composition "H(38) C(29) N(8) O(6) S"
-xref: username_of_poster "Sandeep"
-xref: group_of_poster ""
-xref: date_time_posted "2007-09-14 23:07:12"
-xref: date_time_modified "2007-10-03 15:42:46"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "S"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:775
-name: Carboxymethyl:13C(2)
-def: "Iodoacetic acid derivative w/ 13C label." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=775]
-synonym: "Carboxymethylation w/ 13C label" RELATED []
-xref: record_id "775"
-xref: delta_mono_mass "60.012189"
-xref: delta_avge_mass "60.0214"
-xref: delta_composition "H(2) 13C(2) O(2)"
-xref: username_of_poster "mpcusack"
-xref: group_of_poster ""
-xref: date_time_posted "2007-09-18 19:26:42"
-xref: date_time_modified "2008-06-22 12:00:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:776
-name: NEM:2H(5)
-def: "D5 N-ethylmaleimide on cysteines." [URL:http\://www.chemistry.ucsc.edu/~fink/231/Image118.gif, PMID:12777388, PMID:11813307, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=776]
-synonym: "CysNEM D5" RELATED []
-xref: record_id "776"
-xref: delta_mono_mass "130.079062"
-xref: delta_avge_mass "130.1561"
-xref: delta_composition "H(2) 2H(5) C(6) N O(2)"
-xref: username_of_poster "mpcusack"
-xref: group_of_poster ""
-xref: date_time_posted "2007-09-18 19:49:39"
-xref: date_time_modified "2007-09-28 10:37:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:792
-name: AEC-MAEC:2H(4)
-def: "Deuterium cysteamine modification to S or T." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=792]
-xref: record_id "792"
-xref: delta_mono_mass "63.044462"
-xref: delta_avge_mass "63.158"
-xref: delta_composition "H 2H(4) C(2) N O(-1) S"
-xref: username_of_poster "zwang23"
-xref: group_of_poster ""
-xref: date_time_posted "2007-10-03 19:41:19"
-xref: date_time_modified "2007-10-08 13:44:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:793
-name: Hex(1)HexNAc(1)
-def: "Hex1HexNAc1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=793]
-xref: record_id "793"
-xref: delta_mono_mass "365.132196"
-xref: delta_avge_mass "365.3331"
-xref: delta_composition "Hex HexNAc"
-xref: username_of_poster "julienjardin"
-xref: group_of_poster ""
-xref: date_time_posted "2007-10-12 13:16:23"
-xref: date_time_modified "2017-11-23 13:04:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_366_mono_mass "365.132196"
-xref: spec_1_neutral_loss_366_avge_mass "365.3331"
-xref: spec_1_neutral_loss_366_flag "false"
-xref: spec_1_neutral_loss_366_composition "Hex HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_366_mono_mass "365.132196"
-xref: spec_1_neutral_loss_366_avge_mass "365.3331"
-xref: spec_1_neutral_loss_366_flag "false"
-xref: spec_1_neutral_loss_366_composition "Hex HexNAc"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_misc_notes "Not reported for human proteins"
-xref: spec_2_neutral_loss_366_mono_mass "365.132196"
-xref: spec_2_neutral_loss_366_avge_mass "365.3331"
-xref: spec_2_neutral_loss_366_flag "false"
-xref: spec_2_neutral_loss_366_composition "Hex HexNAc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:799
-name: Label:13C(6)+GG
-def: "13C6 labeled ubiquitinylation residue." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=799]
-comment: The two glycine residues left on SILAC labeled ubiquitinylated lysine after tryptic digestion.
-xref: record_id "799"
-xref: delta_mono_mass "120.063056"
-xref: delta_avge_mass "120.0586"
-xref: delta_composition "H(6) C(-2) 13C(6) N(2) O(2)"
-xref: username_of_poster "glick2"
-xref: group_of_poster ""
-xref: date_time_posted "2007-12-02 22:45:39"
-xref: date_time_modified "2014-07-09 16:53:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:800
-name: Biotin:Thermo-21345
-def: "Was PentylamineBiotin." [URL:http\://www.piercenet.com/Products/Browse.cfm?fldID=01031206, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=800]
-synonym: "Used for labeling glutamine-donor substrate of transglutaminase" RELATED []
-xref: record_id "800"
-xref: delta_mono_mass "311.166748"
-xref: delta_avge_mass "311.4429"
-xref: delta_composition "H(25) C(15) N(3) O(2) S"
-xref: username_of_poster "mengyi"
-xref: group_of_poster ""
-xref: date_time_posted "2007-12-03 13:56:58"
-xref: date_time_modified "2015-01-21 09:40:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:801
-name: Pentylamine
-def: "Labeling transglutaminase substrate on glutamine side chain." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=801]
-xref: record_id "801"
-xref: delta_mono_mass "70.07825"
-xref: delta_avge_mass "70.1329"
-xref: delta_composition "H(10) C(5)"
-xref: username_of_poster "mengyi"
-xref: group_of_poster ""
-xref: date_time_posted "2007-12-05 11:08:02"
-xref: date_time_modified "2021-07-20 13:24:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:811
-name: Biotin:Thermo-21360
-def: "Was Biotin-PEO4-hydrazide." [URL:http\://www.piercenet.com/products/browse.cfm?fldID=C4FE82D4-DD06-493C-8EC4-9C1D7F83211B, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=811]
-synonym: "Pierce EZ link biotin hydrazide prod no. 21360" RELATED []
-xref: record_id "811"
-xref: delta_mono_mass "487.246455"
-xref: delta_avge_mass "487.6134"
-xref: delta_composition "H(37) C(21) N(5) O(6) S"
-xref: username_of_poster "MCole18"
-xref: group_of_poster ""
-xref: date_time_posted "2007-12-12 15:23:23"
-xref: date_time_modified "2010-12-03 16:05:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "hydrazide reacts at any activated carboxyl group"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:821
-name: Cy3b-maleimide
-def: "Fluorescent dye that labels cysteines." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=821]
-synonym: "Cy3b meleimide reacted with Cysteine Formula requires confirmation" RELATED []
-xref: record_id "821"
-xref: delta_mono_mass "682.24612"
-xref: delta_avge_mass "682.7852"
-xref: delta_composition "H(38) C(37) N(4) O(7) S"
-xref: username_of_poster "kfinan"
-xref: group_of_poster ""
-xref: date_time_posted "2008-02-01 16:03:09"
-xref: date_time_modified "2012-09-14 23:51:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:822
-name: Gly-loss+Amide
-def: "Enzymatic glycine removal leaving an amidated C-terminus." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=822]
-synonym: "Amidation requires presence of glycine at peptide terminus" RELATED []
-xref: record_id "822"
-xref: delta_mono_mass "-58.005479"
-xref: delta_avge_mass "-58.0361"
-xref: delta_composition "H(-2) C(-2) O(-2)"
-xref: username_of_poster "timothyr"
-xref: group_of_poster ""
-xref: date_time_posted "2008-02-06 09:33:39"
-xref: date_time_modified "2010-07-14 23:15:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Any C-term"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:824
-name: Xlink:BMOE
-def: "Intact or monolink BMOE crosslinker." [URL:http\://tools.thermofisher.com/content/sfs/manuals/MAN0011308_Bismaleimide_CrsLnk_BMOE_BMB_BMH_UG.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=824]
-xref: record_id "824"
-xref: delta_mono_mass "220.048407"
-xref: delta_avge_mass "220.1815"
-xref: delta_composition "H(8) C(10) N(2) O(4)"
-xref: username_of_poster "Larsenmarsen"
-xref: group_of_poster ""
-xref: date_time_posted "2008-02-13 15:28:55"
-xref: date_time_modified "2017-08-18 11:12:14"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:825
-name: Xlink:DFDNB
-def: "Intact DFDNB crosslinker." [URL:http\://tools.thermofisher.com/content/sfs/manuals/MAN0011313_DFDNB_UG.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=825]
-xref: record_id "825"
-xref: delta_mono_mass "163.985807"
-xref: delta_avge_mass "164.0752"
-xref: delta_composition "C(6) N(2) O(4)"
-xref: username_of_poster "Larsenmarsen"
-xref: group_of_poster ""
-xref: date_time_posted "2008-02-13 15:35:40"
-xref: date_time_modified "2017-08-18 11:55:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "R"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Q"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "N"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:827
-name: TMPP-Ac
-def: "Tris(2,4,6-trimethoxyphenyl)phosphonium acetic acid N-hydroxysuccinimide ester derivative." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=827]
-comment: The formula has been reduced from H(34) to H(33) on 13 May 2009 so as to give correct observed m/z values. The charge on the TMPP means that ions have one less proton than would be expected.
-xref: record_id "827"
-xref: delta_mono_mass "572.181134"
-xref: delta_avge_mass "572.5401"
-xref: delta_composition "H(33) C(29) O(10) P"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2008-02-20 14:12:31"
-xref: date_time_modified "2018-06-26 15:22:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:830
-name: Dihydroxyimidazolidine
-def: "Dihydroxy methylglyoxal adduct." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=830]
-xref: record_id "830"
-xref: delta_mono_mass "72.021129"
-xref: delta_avge_mass "72.0627"
-xref: delta_composition "H(4) C(3) O(2)"
-xref: username_of_poster "kimzey"
-xref: group_of_poster ""
-xref: date_time_posted "2008-03-04 00:00:29"
-xref: date_time_modified "2008-05-22 00:32:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Multiple"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:834
-name: Label:2H(4)+Acetyl
-def: "Acetyl 4,4,5,5-D4 Lysine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=834]
-comment: For SILAC experiments, + PTM.
-synonym: "Acetyl_K4" RELATED []
-xref: record_id "834"
-xref: delta_mono_mass "46.035672"
-xref: delta_avge_mass "46.0613"
-xref: delta_composition "H(-2) 2H(4) C(2) O"
-xref: username_of_poster "Raghothama"
-xref: group_of_poster ""
-xref: date_time_posted "2008-03-24 17:25:15"
-xref: date_time_modified "2008-04-02 10:17:08"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "Both isotopiclabel and post translational mod"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:835
-name: Label:13C(6)+Acetyl
-def: "Acetyl 13C(6) Silac label." [URL:http\://www.pil.sdu.dk/silac_intro.htm, PMID:12716131, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=835]
-xref: record_id "835"
-xref: delta_mono_mass "48.030694"
-xref: delta_avge_mass "47.9926"
-xref: delta_composition "H(2) C(-4) 13C(6) O"
-xref: username_of_poster "Raghothama"
-xref: group_of_poster ""
-xref: date_time_posted "2008-03-24 17:33:44"
-xref: date_time_modified "2008-04-02 10:14:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "SILAC and PTM"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:836
-name: Label:13C(6)15N(2)+Acetyl
-def: "Acetyl_13C(6) 15N(2) Silac label." [URL:http\://www.pil.sdu.dk/silac_intro.htm, PMID:12716131, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=836]
-synonym: "Acetyl_heavy lysine" RELATED []
-xref: record_id "836"
-xref: delta_mono_mass "50.024764"
-xref: delta_avge_mass "49.9794"
-xref: delta_composition "H(2) C(-4) 13C(6) N(-2) 15N(2) O"
-xref: username_of_poster "Raghothama"
-xref: group_of_poster ""
-xref: date_time_posted "2008-03-24 17:35:52"
-xref: date_time_modified "2008-04-02 10:13:59"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "Used in SILAC experiment"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:837
-name: Arg->Npo
-def: "Arginine replacement by Nitropyrimidyl ornithine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=837]
-xref: record_id "837"
-xref: delta_mono_mass "80.985078"
-xref: delta_avge_mass "81.0297"
-xref: delta_composition "H(-1) C(3) N O(2)"
-xref: username_of_poster "Kramerh"
-xref: group_of_poster ""
-xref: date_time_posted "2008-04-10 15:35:22"
-xref: date_time_modified "2008-04-21 18:30:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:846
-name: EQIGG
-def: "Sumo mutant Smt3-WT tail following trypsin digestion." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=846]
-synonym: "Sumoylation" RELATED []
-xref: record_id "846"
-xref: delta_mono_mass "484.228162"
-xref: delta_avge_mass "484.5035"
-xref: delta_composition "H(32) C(20) N(6) O(8)"
-xref: username_of_poster "Magnojunqueira"
-xref: group_of_poster ""
-xref: date_time_posted "2008-05-13 16:56:23"
-xref: date_time_modified "2008-05-17 18:58:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:848
-name: Arg2PG
-def: "Adduct of phenylglyoxal with Arg." [PMID:11945751, PMID:11698400, PMID:5723461, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=848]
-xref: record_id "848"
-xref: delta_mono_mass "266.057909"
-xref: delta_avge_mass "266.2482"
-xref: delta_composition "H(10) C(16) O(4)"
-xref: username_of_poster "Kramerh"
-xref: group_of_poster ""
-xref: date_time_posted "2008-05-16 11:07:51"
-xref: date_time_modified "2008-11-21 18:13:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "The reaction product of Arg with phenylglyoxal has been shown to be a 2:1 adduct"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:849
-name: cGMP
-def: "S-guanylation." [PMID:17906641, PMID:15063129, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=849]
-comment: Protein which is posttranslationally modified by the attachment of cGMP on the sulfur atom of Cys or hydroxyl group of Ser residues.
-xref: record_id "849"
-xref: delta_mono_mass "343.031785"
-xref: delta_avge_mass "343.1895"
-xref: delta_composition "H(10) C(10) N(5) O(7) P"
-xref: username_of_poster "atsushiirie"
-xref: group_of_poster ""
-xref: date_time_posted "2008-06-21 09:02:53"
-xref: date_time_modified "2014-02-08 02:24:10"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:851
-name: cGMP+RMP-loss
-def: "S-guanylation-2." [PMID:17906641, PMID:15063129, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=851]
-comment: Protein which is posttranslationally modified by the attachment of cGMP that has lost ribose 3\',5\'-cyclic monophosphate moiety on the sulfur atom of Cys or hydroxyl group of Ser.
-xref: record_id "851"
-xref: delta_mono_mass "150.041585"
-xref: delta_avge_mass "150.1182"
-xref: delta_composition "H(4) C(5) N(5) O"
-xref: username_of_poster "atsushiirie"
-xref: group_of_poster ""
-xref: date_time_posted "2008-06-21 09:06:56"
-xref: date_time_modified "2009-05-24 20:03:08"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:853
-name: Label:2H(4)+GG
-def: "Ubiquitination 2H4 lysine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=853]
-xref: record_id "853"
-xref: delta_mono_mass "118.068034"
-xref: delta_avge_mass "118.1273"
-xref: delta_composition "H(2) 2H(4) C(4) N(2) O(2)"
-xref: username_of_poster "Raghothama"
-xref: group_of_poster ""
-xref: date_time_posted "2008-06-27 14:28:36"
-xref: date_time_modified "2014-07-09 16:52:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:859
-name: MG-H1
-def: "Methylglyoxal-derived hydroimidazolone." [PMID:15377717, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=859]
-xref: record_id "859"
-xref: delta_mono_mass "54.010565"
-xref: delta_avge_mass "54.0474"
-xref: delta_composition "H(2) C(3) O"
-xref: username_of_poster "AndrewW"
-xref: group_of_poster ""
-xref: date_time_posted "2008-07-24 14:41:07"
-xref: date_time_modified "2008-07-31 17:14:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:860
-name: G-H1
-def: "Glyoxal-derived hydroimiadazolone." [PMID:17143934, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=860]
-xref: record_id "860"
-xref: delta_mono_mass "39.994915"
-xref: delta_avge_mass "40.0208"
-xref: delta_composition "C(2) O"
-xref: username_of_poster "AndrewW"
-xref: group_of_poster ""
-xref: date_time_posted "2008-07-24 14:44:11"
-xref: date_time_modified "2008-07-31 17:16:39"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:861
-name: ZGB
-def: "NHS ester linked Green Fluorescent Bodipy Dye." [URL:http\://www.zdye.com/, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=861]
-xref: record_id "861"
-xref: delta_mono_mass "758.380841"
-xref: delta_avge_mass "758.7261"
-xref: delta_composition "H(53) B C(37) N(6) O(6) F(2) S"
-xref: username_of_poster "JBowden"
-xref: group_of_poster ""
-xref: date_time_posted "2008-07-30 14:51:06"
-xref: date_time_modified "2008-09-22 21:42:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:862
-name: Label:13C(1)2H(3)
-def: "SILAC." [URL:http\://www.pil.sdu.dk/silac_intro.htm, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=862]
-xref: record_id "862"
-xref: delta_mono_mass "4.022185"
-xref: delta_avge_mass "4.0111"
-xref: delta_composition "H(-3) 2H(3) C(-1) 13C"
-xref: username_of_poster "msalek"
-xref: group_of_poster ""
-xref: date_time_posted "2008-08-11 13:43:25"
-xref: date_time_modified "2008-08-14 18:16:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "Isotopic labeled methionine SILAC"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:864
-name: Label:13C(6)15N(2)+GG
-def: "13C(6) 15N(2) Lysine glygly." [PMID:12716131, URL:http\://www.pil.sdu.dk/silac_intro.htm, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=864]
-synonym: "heavy glygly lysine" RELATED []
-xref: record_id "864"
-xref: delta_mono_mass "122.057126"
-xref: delta_avge_mass "122.0454"
-xref: delta_composition "H(6) C(-2) 13C(6) 15N(2) O(2)"
-xref: username_of_poster "Raghothama"
-xref: group_of_poster ""
-xref: date_time_posted "2008-08-13 21:56:52"
-xref: date_time_modified "2014-07-09 16:53:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "Used in SILAC PTM (glygly) experiment"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:866
-name: ICPL:13C(6)2H(4)
-def: "Bruker Daltonics SERVA-ICPL(TM) quantification chemistry, +10 Da form." [URL:http\://www.bdal.de/life-science-tools/care-consumables-more/icpl-kit.html, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=866]
-comment: Attention: As the digest is typically applied AFTER ICPL labeling, only ProteinN-term labeling and Lys-specific labeling is applied.
-synonym: "ICPL_10" RELATED []
-xref: record_id "866"
-xref: delta_mono_mass "115.0667"
-xref: delta_avge_mass "115.0747"
-xref: delta_composition "H(-1) 2H(4) 13C(6) N O"
-xref: username_of_poster "suckau"
-xref: group_of_poster ""
-xref: date_time_posted "2008-09-03 15:17:21"
-xref: date_time_modified "2008-09-12 11:59:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_2_misc_notes "Use when labelling pre-digest"
-xref: spec_3_group "3"
-xref: spec_3_hidden "0"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Use when labelling post-digest"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:876
-name: QEQTGG
-def: "SUMOylation by SUMO-1." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=876]
-synonym: "GlnGluGlnThrGlyGly" RELATED []
-xref: record_id "876"
-xref: delta_mono_mass "600.250354"
-xref: delta_avge_mass "600.5789"
-xref: delta_composition "H(36) C(23) N(8) O(11)"
-xref: username_of_poster "oosula"
-xref: group_of_poster ""
-xref: date_time_posted "2008-09-09 17:02:45"
-xref: date_time_modified "2011-11-25 13:05:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_1_misc_notes "This peptide is generated from a trypsin/chymotrypsin dual digest."
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:877
-name: QQQTGG
-def: "SUMOylation by SUMO-2/3." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=877]
-synonym: "GlnGlnGlnThrGlyGly" RELATED []
-xref: record_id "877"
-xref: delta_mono_mass "599.266339"
-xref: delta_avge_mass "599.5942"
-xref: delta_composition "H(37) C(23) N(9) O(10)"
-xref: username_of_poster "oosula"
-xref: group_of_poster ""
-xref: date_time_posted "2008-09-09 17:09:04"
-xref: date_time_modified "2008-09-19 19:06:46"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_1_misc_notes "This peptide is generated from a trypsin/chymotrypsin dual digest"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:884
-name: Biotin:Thermo-21325
-def: "Was ChromoBiotin." [URL:http\://www.piercenet.com/Products/Browse.cfm?fldID=44B1F9DF-B306-4278-B292-6CDB5B3B9D53, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=884]
-synonym: "EZ-Link NHS-Chromogenic Biotin" RELATED []
-xref: record_id "884"
-xref: delta_mono_mass "695.310118"
-xref: delta_avge_mass "695.8288"
-xref: delta_composition "H(45) C(34) N(7) O(7) S"
-xref: username_of_poster "chens002"
-xref: group_of_poster ""
-xref: date_time_posted "2008-10-20 13:26:20"
-xref: date_time_modified "2010-12-03 16:04:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:885
-name: Label:13C(1)2H(3)+Oxidation
-def: "Oxidised methionine 13C(1)2H(3) SILAC label." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=885]
-xref: record_id "885"
-xref: delta_mono_mass "20.0171"
-xref: delta_avge_mass "20.0105"
-xref: delta_composition "H(-3) 2H(3) C(-1) 13C O"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2008-10-24 09:47:20"
-xref: date_time_modified "2009-09-25 13:15:07"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Multiple"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:886
-name: HydroxymethylOP
-def: "2-ammonio-6-[4-(hydroxymethyl)-3-oxidopyridinium-1-yl]- hexanoate." [PMID:12595094, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=886]
-xref: record_id "886"
-xref: delta_mono_mass "108.021129"
-xref: delta_avge_mass "108.0948"
-xref: delta_composition "H(4) C(6) O(2)"
-xref: username_of_poster "AndrewW"
-xref: group_of_poster ""
-xref: date_time_posted "2008-11-03 14:35:36"
-xref: date_time_modified "2008-11-09 17:49:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_1_misc_notes "Advanced Glycation Endproduct"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:887
-name: MDCC
-def: "Covalent linkage of maleimidyl coumarin probe (Molecular Probes D-10253)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=887]
-comment: MDCC is used extensively as a fluorescent probe to report changes in protein conformation.
-synonym: "CAS 156571-46-9 7-diethylamino-3-((((2-maleimidyl)ethyl)amino)carbonyl)coumarin" RELATED []
-xref: record_id "887"
-xref: delta_mono_mass "383.148121"
-xref: delta_avge_mass "383.3978"
-xref: delta_composition "H(21) C(20) N(3) O(5)"
-xref: username_of_poster "shartson"
-xref: group_of_poster ""
-xref: date_time_posted "2008-12-03 16:20:46"
-xref: date_time_modified "2008-12-05 09:32:22"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "Due to the mechanism of maleimidyl modification of Cys, the molecular weight of MDCC equals the mass shift created upon crossllinking (no chemical leaving group). During MS/MS, MDCC can reasonably be predicted to fragment readily and at various positions."
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:888
-name: mTRAQ
-def: "MTRAQ light." [URL:http\://www3.appliedbiosystems.com/cms/groups/psm_support/documents/generaldocuments/cms_054141.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=888]
-synonym: "Applied Biosystems mTRAQ(TM) reagent" RELATED []
-xref: record_id "888"
-xref: delta_mono_mass "140.094963"
-xref: delta_avge_mass "140.183"
-xref: delta_composition "H(12) C(7) N(2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2008-12-04 13:50:02"
-xref: date_time_modified "2011-11-25 10:30:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "0"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Low abundance"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "H"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "Very low abundance"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "S"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Isotopic label"
-xref: spec_5_misc_notes "Very low abundance"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "T"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Isotopic label"
-xref: spec_6_misc_notes "Very low abundance"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:889
-name: mTRAQ:13C(3)15N(1)
-def: "MTRAQ medium." [URL:http\://www3.appliedbiosystems.com/cms/groups/psm_support/documents/generaldocuments/cms_054141.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=889]
-synonym: "mTRAQ medium is identical to iTRAQ4plex 117 Applied Biosystems mTRAQ(TM) reagent" RELATED []
-xref: record_id "889"
-xref: delta_mono_mass "144.102063"
-xref: delta_avge_mass "144.1544"
-xref: delta_composition "H(12) C(4) 13C(3) N 15N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2008-12-05 09:26:02"
-xref: date_time_modified "2011-11-25 10:34:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "0"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Low abundance"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "H"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "Very low abundance"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "S"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Isotopic label"
-xref: spec_5_misc_notes "Very low abundance"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "T"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Isotopic label"
-xref: spec_6_misc_notes "Very low abundance"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:890
-name: DyLight-maleimide
-def: "Thiol-reactive dye for fluorescence labelling of proteins." [URL:http\://www.piercenet.com/files/1964as4.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=890]
-xref: record_id "890"
-xref: delta_mono_mass "940.1999"
-xref: delta_avge_mass "941.0762"
-xref: delta_composition "H(48) C(39) N(4) O(15) S(4)"
-xref: username_of_poster "anikolakakis"
-xref: group_of_poster ""
-xref: date_time_posted "2008-12-05 15:23:15"
-xref: date_time_modified "2008-12-15 12:17:39"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:891
-name: Methyl-PEO12-Maleimide
-def: "Methyl-PEO12-Maleimide." [URL:http\://www.piercenet.com/files/1768dh5.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=891]
-xref: record_id "891"
-xref: delta_mono_mass "710.383719"
-xref: delta_avge_mass "710.8073"
-xref: delta_composition "H(58) C(32) N(2) O(15)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2008-12-09 11:02:18"
-xref: date_time_modified "2008-12-15 12:15:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:893
-name: CarbamidomethylDTT
-def: "Carbamidomethylated DTT modification of cysteine." [PMID:18653769, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=893]
-xref: record_id "893"
-xref: delta_mono_mass "209.018035"
-xref: delta_avge_mass "209.2864"
-xref: delta_composition "H(11) C(6) N O(3) S(2)"
-xref: username_of_poster "chalkley"
-xref: group_of_poster ""
-xref: date_time_posted "2009-01-09 01:39:37"
-xref: date_time_modified "2017-06-15 14:11:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:894
-name: CarboxymethylDTT
-def: "Carboxymethylated DTT modification of cysteine." [PMID:18653769, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=894]
-xref: record_id "894"
-xref: delta_mono_mass "210.00205"
-xref: delta_avge_mass "210.2712"
-xref: delta_composition "H(10) C(6) O(4) S(2)"
-xref: username_of_poster "chalkley"
-xref: group_of_poster ""
-xref: date_time_posted "2009-01-09 01:43:09"
-xref: date_time_modified "2009-01-10 19:03:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:895
-name: Biotin-PEG-PRA
-def: "Biotin polyethyleneoxide (n=3) alkyne." [URL:http\://etd.caltech.edu/etd/available/etd-09132005-120123/unrestricted/Chapter2.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=895]
-comment: Methionine (C5H11NO2S) is substituted in cell culture by Azidohomoalanine (C4H8N4O2). The azido group reacts with an alkyne group attached to a linker (PEO) with a biotin group at the end (C27H45N5O7S). As a result the side chain of Met (C3H7S) is substitued by C29H49N8O7S.
-xref: record_id "895"
-xref: delta_mono_mass "578.317646"
-xref: delta_avge_mass "578.6611"
-xref: delta_composition "H(42) C(26) N(8) O(7)"
-xref: username_of_poster "Larsenmarsen"
-xref: group_of_poster ""
-xref: date_time_posted "2009-01-19 10:54:58"
-xref: date_time_modified "2009-02-06 16:50:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:896
-name: Met->Aha
-def: "Methionine replacement by azido homoalanine." [PMID:16281315, PMID:11752401, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=896]
-xref: record_id "896"
-xref: delta_mono_mass "-4.986324"
-xref: delta_avge_mass "-5.0794"
-xref: delta_composition "H(-3) C(-1) N(3) S(-1)"
-xref: username_of_poster "Kramerh"
-xref: group_of_poster ""
-xref: date_time_posted "2009-01-30 14:52:20"
-xref: date_time_modified "2009-02-06 16:38:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Non-standard residue"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:897
-name: Label:15N(4)
-def: "SILAC 15N(4)." [URL:http\://www.pil.sdu.dk/silac_intro.htm, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=897]
-synonym: "Metabolic labeling with ammonium sulfate (15N)" RELATED []
-xref: record_id "897"
-xref: delta_mono_mass "3.98814"
-xref: delta_avge_mass "3.9736"
-xref: delta_composition "N(-4) 15N(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2009-02-06 15:29:55"
-xref: date_time_modified "2011-11-21 14:26:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:898
-name: pyrophospho
-def: "Pyrophosphorylation of Ser/Thr." [PMID:17873058, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=898]
-xref: record_id "898"
-xref: delta_mono_mass "159.932662"
-xref: delta_avge_mass "159.9598"
-xref: delta_composition "H(2) O(6) P(2)"
-xref: username_of_poster "Kramerh"
-xref: group_of_poster ""
-xref: date_time_posted "2009-02-23 20:54:00"
-xref: date_time_modified "2009-11-11 09:39:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_1_neutral_loss_177_mono_mass "176.935402"
-xref: spec_1_neutral_loss_177_avge_mass "176.9671"
-xref: spec_1_neutral_loss_177_flag "false"
-xref: spec_1_neutral_loss_177_composition "H(3) O(7) P(2)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_2_neutral_loss_177_mono_mass "176.935402"
-xref: spec_2_neutral_loss_177_avge_mass "176.9671"
-xref: spec_2_neutral_loss_177_flag "false"
-xref: spec_2_neutral_loss_177_composition "H(3) O(7) P(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:899
-name: Met->Hpg
-def: "Methionine replacement by homopropargylglycine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=899]
-xref: record_id "899"
-xref: delta_mono_mass "-21.987721"
-xref: delta_avge_mass "-22.0702"
-xref: delta_composition "H(-2) C S(-1)"
-xref: username_of_poster "Kramerh"
-xref: group_of_poster ""
-xref: date_time_posted "2009-02-24 17:11:44"
-xref: date_time_modified "2009-03-13 16:00:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Non-standard residue"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:901
-name: 4AcAllylGal
-def: "2,3,4,6-tetra-O-Acetyl-1-allyl-alpha-D-galactopyranoside modification of cysteine." [PMID:18275052, PMID:19798718, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=901]
-xref: record_id "901"
-xref: delta_mono_mass "372.142033"
-xref: delta_avge_mass "372.3671"
-xref: delta_composition "H(24) C(17) O(9)"
-xref: username_of_poster "paolo.nanni"
-xref: group_of_poster ""
-xref: date_time_posted "2009-03-06 16:08:43"
-xref: date_time_modified "2014-06-23 14:32:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:902
-name: DimethylArsino
-def: "Reaction with dimethylarsinous (AsIII) acid." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=902]
-comment: Protein from animals exposed to organoarsenicals.
-xref: record_id "902"
-xref: delta_mono_mass "103.960719"
-xref: delta_avge_mass "103.9827"
-xref: delta_composition "H(5) C(2) As"
-xref: username_of_poster "dashford"
-xref: group_of_poster ""
-xref: date_time_posted "2009-03-09 17:03:27"
-xref: date_time_modified "2009-03-13 15:59:22"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:903
-name: Lys->CamCys
-def: "Lys->Cys substitution and carbamidomethylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=903]
-comment: For Brad Strader.
-xref: record_id "903"
-xref: delta_mono_mass "31.935685"
-xref: delta_avge_mass "32.0219"
-xref: delta_composition "H(-4) C(-1) O S"
-xref: username_of_poster "hooverdm"
-xref: group_of_poster ""
-xref: date_time_posted "2009-04-17 14:47:30"
-xref: date_time_modified "2009-05-01 16:47:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Pre-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:904
-name: Phe->CamCys
-def: "Phe->Cys substitution and carbamidomethylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=904]
-comment: For Brad Strader.
-xref: record_id "904"
-xref: delta_mono_mass "12.962234"
-xref: delta_avge_mass "13.0204"
-xref: delta_composition "H(-1) C(-4) N O S"
-xref: username_of_poster "hooverdm"
-xref: group_of_poster ""
-xref: date_time_posted "2009-04-17 14:49:02"
-xref: date_time_modified "2009-07-13 18:16:29"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Pre-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:905
-name: Leu->MetOx
-def: "Leu->Met substitution and sulfoxidation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=905]
-comment: For Brad Strader.
-xref: record_id "905"
-xref: delta_mono_mass "33.951335"
-xref: delta_avge_mass "34.0378"
-xref: delta_composition "H(-2) C(-1) O S"
-xref: username_of_poster "hooverdm"
-xref: group_of_poster ""
-xref: date_time_posted "2009-04-17 14:50:35"
-xref: date_time_modified "2009-05-01 16:47:06"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Pre-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:906
-name: Lys->MetOx
-def: "Lys->Met substitution and sulfoxidation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=906]
-comment: For Brad Strader.
-xref: record_id "906"
-xref: delta_mono_mass "18.940436"
-xref: delta_avge_mass "19.0232"
-xref: delta_composition "H(-3) C(-1) N(-1) O S"
-xref: username_of_poster "hooverdm"
-xref: group_of_poster ""
-xref: date_time_posted "2009-04-17 14:51:35"
-xref: date_time_modified "2009-05-01 16:46:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Pre-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:907
-name: Galactosyl
-def: "Gluconoylation." [URL:http\://www.abrf.org/index.cfm/dm.details?DMID=226&AvgMass=all&Margin=0, PMID:743239, PMID:18083862, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=907]
-xref: record_id "907"
-xref: delta_mono_mass "178.047738"
-xref: delta_avge_mass "178.14"
-xref: delta_composition "O Hex"
-xref: username_of_poster "zientek"
-xref: group_of_poster ""
-xref: date_time_posted "2009-04-21 18:11:24"
-xref: date_time_modified "2015-05-07 11:02:58"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other glycosylation"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Other glycosylation"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:908
-name: Xlink:SMCC[321]
-def: "Monolink of SMCC terminated with 3-(dimethylamino)-1-propylamine." [URL:https\://assets.thermofisher.com/TFS-Assets/LSG/manuals/MAN0011295_SMCC_SulfoSMCC_UG.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=908]
-xref: record_id "908"
-xref: delta_mono_mass "321.205242"
-xref: delta_avge_mass "321.4146"
-xref: delta_composition "H(27) C(17) N(3) O(3)"
-xref: username_of_poster "anikolakakis"
-xref: group_of_poster ""
-xref: date_time_posted "2009-04-23 19:39:42"
-xref: date_time_modified "2017-09-01 14:46:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:910
-name: Bacillosamine
-def: "2,4-diacetamido-2,4,6-trideoxyglucopyranose." [PMID:12186869, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=910]
-synonym: "Asn-linked glycan from Gram-negative Bacterium DATDH" RELATED []
-xref: record_id "910"
-xref: delta_mono_mass "228.111007"
-xref: delta_avge_mass "228.245"
-xref: delta_composition "H(6) C(4) N(2) dHex"
-xref: username_of_poster "rlmoritz"
-xref: group_of_poster ""
-xref: date_time_posted "2009-06-23 18:27:32"
-xref: date_time_modified "2017-11-29 14:04:43"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_229_mono_mass "228.111007"
-xref: spec_1_neutral_loss_229_avge_mass "228.245"
-xref: spec_1_neutral_loss_229_flag "false"
-xref: spec_1_neutral_loss_229_composition "H(6) C(4) N(2) dHex"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:911
-name: MTSL
-def: "Cys modification by (1-oxyl-2,2,5,5-tetramethyl-3-pyrroline-3-methyl)methanesulfonate (MTSL)." [PMID:9335564, PMID:12441112, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=911]
-xref: record_id "911"
-xref: delta_mono_mass "184.07961"
-xref: delta_avge_mass "184.2786"
-xref: delta_composition "H(14) C(9) N O S"
-xref: username_of_poster "Kramerh"
-xref: group_of_poster ""
-xref: date_time_posted "2009-06-25 20:19:40"
-xref: date_time_modified "2009-06-26 11:13:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:912
-name: HNE-BAHAH
-def: "4-hydroxy-2-nonenal and biotinamidohexanoic acid hydrazide, reduced." [PMID:19054759, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=912]
-comment: For Bindu Abraham.
-xref: record_id "912"
-xref: delta_mono_mass "511.319226"
-xref: delta_avge_mass "511.7209"
-xref: delta_composition "H(45) C(25) N(5) O(4) S"
-xref: username_of_poster "hooverdm"
-xref: group_of_poster ""
-xref: date_time_posted "2009-07-13 18:23:28"
-xref: date_time_modified "2009-07-17 17:49:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:914
-name: Methylmalonylation
-def: "Methylmalonylation on Serine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=914]
-comment: Structural isomer to succinyl.
-xref: record_id "914"
-xref: delta_mono_mass "100.016044"
-xref: delta_avge_mass "100.0728"
-xref: delta_composition "H(4) C(4) O(3)"
-xref: username_of_poster "xwei"
-xref: group_of_poster ""
-xref: date_time_posted "2009-07-15 23:43:13"
-xref: date_time_modified "2010-11-24 17:59:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:923
-name: Label:13C(4)15N(2)+GG
-def: "13C(4) 15N(2) Lysine glygly." [PMID:12716131, URL:http\://www.pil.sdu.dk/silac_intro.htm, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=923]
-synonym: "heavy glygly lysine" RELATED []
-xref: record_id "923"
-xref: delta_mono_mass "120.050417"
-xref: delta_avge_mass "120.0601"
-xref: delta_composition "H(6) 13C(4) 15N(2) O(2)"
-xref: username_of_poster "mpcusack"
-xref: group_of_poster ""
-xref: date_time_posted "2009-09-16 21:04:07"
-xref: date_time_modified "2014-07-09 16:53:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "Used in SILAC PTM (glygly) experiment"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:926
-name: ethylamino
-def: "Ethyl amino." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=926]
-comment: Product of beta elimination of phospho- or glycosylated-Ser with addition of ethylamine.
-xref: record_id "926"
-xref: delta_mono_mass "27.047285"
-xref: delta_avge_mass "27.0684"
-xref: delta_composition "H(5) C(2) N O(-1)"
-xref: username_of_poster "cbatthya"
-xref: group_of_poster ""
-xref: date_time_posted "2009-09-17 20:37:18"
-xref: date_time_modified "2009-10-02 18:21:10"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:928
-name: MercaptoEthanol
-def: "2-OH-ethyl thio-Ser." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=928]
-comment: Product of beta elimination of phospho- or glycosylated-Ser with addition of beta Mercapto Ethanol.
-xref: record_id "928"
-xref: delta_mono_mass "60.003371"
-xref: delta_avge_mass "60.1182"
-xref: delta_composition "H(4) C(2) S"
-xref: username_of_poster "cbatthya"
-xref: group_of_poster ""
-xref: date_time_posted "2009-09-17 20:43:13"
-xref: date_time_modified "2009-10-02 18:23:38"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:931
-name: Ethyl+Deamidated
-def: "Deamidation followed by esterification with ethanol." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=931]
-xref: record_id "931"
-xref: delta_mono_mass "29.015316"
-xref: delta_avge_mass "29.0379"
-xref: delta_composition "H(3) C(2) N(-1) O"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2009-09-22 11:05:21"
-xref: date_time_modified "2012-08-06 14:58:24"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "Q"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:932
-name: VFQQQTGG
-def: "SUMOylation by SUMO-2/3 (formic acid cleavage)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=932]
-synonym: "ValPheGlnGlnGlnThrGlyGly" RELATED []
-xref: record_id "932"
-xref: delta_mono_mass "845.403166"
-xref: delta_avge_mass "845.8991"
-xref: delta_composition "H(55) C(37) N(11) O(12)"
-xref: username_of_poster "oosula"
-xref: group_of_poster ""
-xref: date_time_posted "2009-09-24 16:11:11"
-xref: date_time_modified "2010-02-02 18:25:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_1_misc_notes "This peptide is generated from a formic acid digest"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:933
-name: VIEVYQEQTGG
-def: "SUMOylation by SUMO-1 (formic acid cleavage)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=933]
-synonym: "ValIleGluValTyrGlnGluGlnThrGlyGly" RELATED []
-xref: record_id "933"
-xref: delta_mono_mass "1203.577168"
-xref: delta_avge_mass "1204.2859"
-xref: delta_composition "H(81) C(53) N(13) O(19)"
-xref: username_of_poster "oosula"
-xref: group_of_poster ""
-xref: date_time_posted "2009-09-24 16:15:34"
-xref: date_time_modified "2009-10-02 18:31:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:934
-name: AMTzHexNAc2
-def: "Photocleavable Biotin + GalNAz on O-GlcNAc." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=934]
-xref: record_id "934"
-xref: delta_mono_mass "502.202341"
-xref: delta_avge_mass "502.4757"
-xref: delta_composition "H(30) C(19) N(6) O(10)"
-xref: username_of_poster "mskim"
-xref: group_of_poster ""
-xref: date_time_posted "2009-10-08 18:05:00"
-xref: date_time_modified "2010-10-03 13:45:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:935
-name: Atto495Maleimide
-def: "High molecular absorption maleimide label for proteins." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=935]
-xref: record_id "935"
-xref: delta_mono_mass "474.250515"
-xref: delta_avge_mass "474.5747"
-xref: delta_composition "H(32) C(27) N(5) O(3)"
-xref: username_of_poster "anikolakakis"
-xref: group_of_poster ""
-xref: date_time_posted "2009-10-14 18:48:56"
-xref: date_time_modified "2009-10-16 14:34:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:936
-name: Chlorination
-def: "Chlorination of tyrosine residues." [PMID:14660678, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=936]
-xref: record_id "936"
-xref: delta_mono_mass "33.961028"
-xref: delta_avge_mass "34.4451"
-xref: delta_composition "H(-1) Cl"
-xref: username_of_poster "Bryan"
-xref: group_of_poster ""
-xref: date_time_posted "2009-10-15 17:07:41"
-xref: date_time_modified "2017-11-08 16:03:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "W"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:937
-name: dichlorination
-def: "Dichlorination." [PMID:11733505, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=937]
-xref: record_id "937"
-xref: delta_mono_mass "67.922055"
-xref: delta_avge_mass "68.8901"
-xref: delta_composition "H(-2) Cl(2)"
-xref: username_of_poster "Bryan"
-xref: group_of_poster ""
-xref: date_time_posted "2009-10-15 17:12:42"
-xref: date_time_modified "2014-05-19 10:13:24"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:938
-name: AROD
-def: "Cysteine modifier." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=938]
-comment: The electrophilic moiety of the chemical forms a direct bond with the thiol bond of the cysteine. As a result, there are no losses of elements and the final adduct has the monoisotopic mass of the chemical at 820.3360 added to a cysteine at SH side chain.
-xref: record_id "938"
-xref: delta_mono_mass "820.336015"
-xref: delta_avge_mass "820.979"
-xref: delta_composition "H(52) C(35) N(10) O(9) S(2)"
-xref: username_of_poster "hbromage"
-xref: group_of_poster ""
-xref: date_time_posted "2009-10-15 19:27:20"
-xref: date_time_modified "2009-10-16 14:41:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:939
-name: Cys->methylaminoAla
-def: "Carbamidomethylated Cys that undergoes beta-elimination and Michael addition of methylamine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=939]
-xref: record_id "939"
-xref: delta_mono_mass "-2.945522"
-xref: delta_avge_mass "-3.0238"
-xref: delta_composition "H(3) C N S(-1)"
-xref: username_of_poster "cbatthya"
-xref: group_of_poster ""
-xref: date_time_posted "2009-10-16 13:50:33"
-xref: date_time_modified "2009-10-16 14:44:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:940
-name: Cys->ethylaminoAla
-def: "Carbamidomethylated Cys that undergoes beta-elimination and Michael addition of ethylamine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=940]
-xref: record_id "940"
-xref: delta_mono_mass "11.070128"
-xref: delta_avge_mass "11.0028"
-xref: delta_composition "H(5) C(2) N S(-1)"
-xref: username_of_poster "cbatthya"
-xref: group_of_poster ""
-xref: date_time_posted "2009-10-16 13:53:46"
-xref: date_time_modified "2009-10-16 14:44:21"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:941
-name: DNPS
-def: "2,4-Dinitrobenzenesulfenyl." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=941]
-synonym: "Trp modification with 2,4-Dinitrobenzenesulfenyl" RELATED []
-xref: record_id "941"
-xref: delta_mono_mass "198.981352"
-xref: delta_avge_mass "199.164"
-xref: delta_composition "H(3) C(6) N(2) O(4) S"
-xref: username_of_poster "odra.pinato"
-xref: group_of_poster ""
-xref: date_time_posted "2009-10-19 13:08:56"
-xref: date_time_modified "2009-10-30 18:23:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "Fontana A. Biochemistry. vol 7. 980-986 (1968)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "W"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_2_misc_notes "derivatization of Trp residues using the 2,4-dinitrophenyl-sulfenyl chloride (DNPS-Cl) reagent, that leads to a Trp derivative with the DNPS label attached at 2-position of the indole nucleus."
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:942
-name: SulfoGMBS
-def: "High molecular absorption label for proteins." [URL:http\://www.piercenet.com/files/1763dh4.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=942]
-xref: record_id "942"
-xref: delta_mono_mass "458.162391"
-xref: delta_avge_mass "458.5306"
-xref: delta_composition "H(26) C(22) N(4) O(5) S"
-xref: username_of_poster "anikolakakis"
-xref: group_of_poster ""
-xref: date_time_posted "2009-10-26 19:28:04"
-xref: date_time_modified "2009-11-13 17:02:06"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:943
-name: DimethylamineGMBS
-def: "Modified GMBS X linker." [URL:http\://tools.thermofisher.com/content/sfs/manuals/MAN0011551_GMBS_SulfoGMBS_UG.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=943]
-xref: record_id "943"
-xref: delta_mono_mass "267.158292"
-xref: delta_avge_mass "267.3241"
-xref: delta_composition "H(21) C(13) N(3) O(3)"
-xref: username_of_poster "anikolakakis"
-xref: group_of_poster ""
-xref: date_time_posted "2009-11-04 20:26:57"
-xref: date_time_modified "2017-01-18 11:52:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:944
-name: Label:15N(2)2H(9)
-def: "SILAC label." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=944]
-synonym: "Label:15N(2)2H(9)" RELATED []
-xref: record_id "944"
-xref: delta_mono_mass "11.050561"
-xref: delta_avge_mass "11.0423"
-xref: delta_composition "H(-9) 2H(9) N(-2) 15N(2)"
-xref: username_of_poster "mskim"
-xref: group_of_poster ""
-xref: date_time_posted "2009-11-25 22:32:49"
-xref: date_time_modified "2009-12-07 20:03:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:946
-name: LG-anhydrolactam
-def: "Levuglandinyl-lysine anhydrolactam adduct." [PMID:10413514, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=946]
-xref: record_id "946"
-xref: delta_mono_mass "314.188195"
-xref: delta_avge_mass "314.4186"
-xref: delta_composition "H(26) C(20) O(3)"
-xref: username_of_poster "wridenour"
-xref: group_of_poster ""
-xref: date_time_posted "2010-01-12 01:08:28"
-xref: date_time_modified "2011-06-08 18:01:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:947
-name: LG-pyrrole
-def: "Levuglandinyl-lysine pyrrole adduct." [PMID:10413514, URL:http\://www.hmdb.ca/metabolites/HMDB0005079, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=947]
-xref: record_id "947"
-xref: delta_mono_mass "316.203845"
-xref: delta_avge_mass "316.4345"
-xref: delta_composition "H(28) C(20) O(3)"
-xref: username_of_poster "wridenour"
-xref: group_of_poster ""
-xref: date_time_posted "2010-01-12 01:12:38"
-xref: date_time_modified "2020-01-21 14:42:42"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "C"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-xref: spec_3_misc_notes "15-deoxy-PGJ2 (15d-PGJ2) influences multiple signaling pathways by covalently binding with key signaling molecules"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:948
-name: LG-anhyropyrrole
-def: "Levuglandinyl-lysine anhyropyrrole adduct." [PMID:10413514, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=948]
-xref: record_id "948"
-xref: delta_mono_mass "298.19328"
-xref: delta_avge_mass "298.4192"
-xref: delta_composition "H(26) C(20) O(2)"
-xref: username_of_poster "wridenour"
-xref: group_of_poster ""
-xref: date_time_posted "2010-01-12 01:14:46"
-xref: date_time_modified "2011-06-08 17:59:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:949
-name: 3-deoxyglucosone
-def: "Condensation product of 3-deoxyglucosone." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=949]
-xref: record_id "949"
-xref: delta_mono_mass "144.042259"
-xref: delta_avge_mass "144.1253"
-xref: delta_composition "H(8) C(6) O(4)"
-xref: username_of_poster "kimzey"
-xref: group_of_poster ""
-xref: date_time_posted "2010-01-15 18:19:17"
-xref: date_time_modified "2024-08-12 10:04:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Multiple"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:950
-name: Cation:Li
-def: "Replacement of proton by lithium." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=950]
-xref: record_id "950"
-xref: delta_mono_mass "6.008178"
-xref: delta_avge_mass "5.9331"
-xref: delta_composition "H(-1) Li"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2010-01-20 12:17:12"
-xref: date_time_modified "2010-01-20 12:17:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:951
-name: Cation:Ca[II]
-def: "Replacement of 2 protons by calcium." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=951]
-xref: record_id "951"
-xref: delta_mono_mass "37.946941"
-xref: delta_avge_mass "38.0621"
-xref: delta_composition "H(-2) Ca"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2010-01-20 12:20:03"
-xref: date_time_modified "2010-01-20 12:36:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:952
-name: Cation:Fe[II]
-def: "Replacement of 2 protons by iron." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=952]
-xref: record_id "952"
-xref: delta_mono_mass "53.919289"
-xref: delta_avge_mass "53.8291"
-xref: delta_composition "H(-2) Fe"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2010-01-20 12:21:03"
-xref: date_time_modified "2010-01-20 12:21:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:953
-name: Cation:Ni[II]
-def: "Replacement of 2 protons by nickel." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=953]
-xref: record_id "953"
-xref: delta_mono_mass "55.919696"
-xref: delta_avge_mass "56.6775"
-xref: delta_composition "H(-2) Ni"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2010-01-20 12:22:52"
-xref: date_time_modified "2010-01-20 12:22:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:954
-name: Cation:Zn[II]
-def: "Replacement of 2 protons by zinc." [URL:http\://www.uniprot.org/uniprot/P07509, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=954]
-xref: record_id "954"
-xref: delta_mono_mass "61.913495"
-xref: delta_avge_mass "63.3931"
-xref: delta_composition "H(-2) Zn"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2010-01-20 12:23:59"
-xref: date_time_modified "2015-03-19 09:31:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "H"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:955
-name: Cation:Ag
-def: "Replacement of proton by silver." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=955]
-xref: record_id "955"
-xref: delta_mono_mass "105.897267"
-xref: delta_avge_mass "106.8603"
-xref: delta_composition "H(-1) Ag"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2010-01-20 12:30:59"
-xref: date_time_modified "2010-01-20 12:30:59"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:956
-name: Cation:Mg[II]
-def: "Replacement of 2 protons by magnesium." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=956]
-xref: record_id "956"
-xref: delta_mono_mass "21.969392"
-xref: delta_avge_mass "22.2891"
-xref: delta_composition "H(-2) Mg"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2010-01-20 12:36:18"
-xref: date_time_modified "2010-01-20 12:36:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:957
-name: 2-succinyl
-def: "S-(2-succinyl) cysteine." [PMID:18448829, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=957]
-xref: record_id "957"
-xref: delta_mono_mass "116.010959"
-xref: delta_avge_mass "116.0722"
-xref: delta_composition "H(4) C(4) O(4)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2010-01-26 09:57:53"
-xref: date_time_modified "2010-10-15 15:51:20"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:958
-name: Propargylamine
-def: "Propargylamine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=958]
-xref: record_id "958"
-xref: delta_mono_mass "37.031634"
-xref: delta_avge_mass "37.0632"
-xref: delta_composition "H(3) C(3) N O(-1)"
-xref: username_of_poster "ywswansea"
-xref: group_of_poster ""
-xref: date_time_posted "2010-01-26 14:37:33"
-xref: date_time_modified "2010-02-01 09:26:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Any C-term"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "D"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "E"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:959
-name: Phosphopropargyl
-def: "Phospho-propargylamine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=959]
-xref: record_id "959"
-xref: delta_mono_mass "116.997965"
-xref: delta_avge_mass "117.0431"
-xref: delta_composition "H(4) C(3) N O(2) P"
-xref: username_of_poster "ywswansea"
-xref: group_of_poster ""
-xref: date_time_posted "2010-01-26 14:42:08"
-xref: date_time_modified "2010-02-01 09:25:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Multiple"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Multiple"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Multiple"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:960
-name: SUMO2135
-def: "SUMOylation by SUMO-1 after tryptic cleavage." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=960]
-synonym: "ELGMEEEDVIEVYQEQTGG" RELATED []
-xref: record_id "960"
-xref: delta_mono_mass "2135.920496"
-xref: delta_avge_mass "2137.2343"
-xref: delta_composition "H(137) C(90) N(21) O(37) S"
-xref: username_of_poster "oosula"
-xref: group_of_poster ""
-xref: date_time_posted "2010-02-02 18:17:15"
-xref: date_time_modified "2010-02-14 11:28:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:961
-name: SUMO3549
-def: "SUMOylation by SUMO-2/3 after tryptic cleavage." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=961]
-synonym: "FDGQPINETDTPAQLEMEDEDTIDVFQQQTGG" RELATED []
-xref: record_id "961"
-xref: delta_mono_mass "3549.536568"
-xref: delta_avge_mass "3551.6672"
-xref: delta_composition "H(224) C(150) N(38) O(60) S"
-xref: username_of_poster "oosula"
-xref: group_of_poster ""
-xref: date_time_posted "2010-02-02 18:21:23"
-xref: date_time_modified "2010-02-14 11:27:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:967
-name: thioacylPA
-def: "Membrane protein extraction." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=967]
-xref: record_id "967"
-xref: delta_mono_mass "159.035399"
-xref: delta_avge_mass "159.2062"
-xref: delta_composition "H(9) C(6) N O(2) S"
-xref: username_of_poster "tmiwamoto"
-xref: group_of_poster ""
-xref: date_time_posted "2010-02-05 06:00:39"
-xref: date_time_modified "2010-04-05 21:31:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:971
-name: maleimide3
-def: "Maleimide-3-saccharide." [PMID:18925771, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=971]
-comment: Created for Bindu Abraham 12/22/09.
-xref: record_id "971"
-xref: delta_mono_mass "969.366232"
-xref: delta_avge_mass "969.8975"
-xref: delta_composition "H(59) C(37) N(7) O(23)"
-xref: username_of_poster "hooverdm"
-xref: group_of_poster ""
-xref: date_time_posted "2010-02-12 17:23:33"
-xref: date_time_modified "2010-04-05 21:30:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:972
-name: maleimide5
-def: "Maleimide-5-saccharide." [PMID:18925771, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=972]
-comment: Created for Bindu Abraham 12/22/09.
-xref: record_id "972"
-xref: delta_mono_mass "1293.471879"
-xref: delta_avge_mass "1294.1787"
-xref: delta_composition "H(79) C(49) N(7) O(33)"
-xref: username_of_poster "hooverdm"
-xref: group_of_poster ""
-xref: date_time_posted "2010-02-12 17:25:52"
-xref: date_time_modified "2010-04-05 21:29:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:973
-name: Puromycin
-def: "Puromycin." [PMID:10666460, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=973]
-comment: Created for Michael (Brad) Strader 2/12/10.
-xref: record_id "973"
-xref: delta_mono_mass "453.212452"
-xref: delta_avge_mass "453.4943"
-xref: delta_composition "H(27) C(22) N(7) O(4)"
-xref: username_of_poster "hooverdm"
-xref: group_of_poster ""
-xref: date_time_posted "2010-02-12 20:50:31"
-xref: date_time_modified "2010-04-12 15:38:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Any C-term"
-xref: spec_1_classification "Co-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:977
-name: Carbofuran
-def: "2,3-dihydro-2,2-dimethyl-7-benzofuranol N-methyl carbamate." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=977]
-xref: record_id "977"
-xref: delta_mono_mass "57.021464"
-xref: delta_avge_mass "57.0513"
-xref: delta_composition "H(3) C(2) N O"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2010-02-24 21:10:32"
-xref: date_time_modified "2021-06-30 18:27:33"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:978
-name: BITC
-def: "Benzyl isothiocyanate." [PMID:22835833, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=978]
-xref: record_id "978"
-xref: delta_mono_mass "149.02992"
-xref: delta_avge_mass "149.2129"
-xref: delta_composition "H(7) C(8) N S"
-xref: username_of_poster "miyoshin"
-xref: group_of_poster ""
-xref: date_time_posted "2010-03-09 09:42:12"
-xref: date_time_modified "2013-04-26 06:26:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:979
-name: PEITC
-def: "Phenethyl isothiocyanate." [PMID:22835833, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=979]
-xref: record_id "979"
-xref: delta_mono_mass "163.04557"
-xref: delta_avge_mass "163.2395"
-xref: delta_composition "H(9) C(9) N S"
-xref: username_of_poster "miyoshin"
-xref: group_of_poster ""
-xref: date_time_posted "2010-03-09 10:06:18"
-xref: date_time_modified "2013-04-26 06:27:10"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:981
-name: glucosone
-def: "Condensation product of glucosone." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=981]
-xref: record_id "981"
-xref: delta_mono_mass "160.037173"
-xref: delta_avge_mass "160.1247"
-xref: delta_composition "H(8) C(6) O(5)"
-xref: username_of_poster "kimzey"
-xref: group_of_poster ""
-xref: date_time_posted "2010-03-31 00:28:53"
-xref: date_time_modified "2010-04-05 21:25:21"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:984
-name: cysTMT
-def: "Native cysteine-reactive Tandem Mass Tag®." [URL:http\://bit.ly/1GBnaC8, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=984]
-comment: This modification describes the native cysteine-reactive cysTMT Reagent without isotopic label. Upon CID, this reagent releases a reporter ion of 126.127725 (monoisotopic mass).
-synonym: "Tandem Mass Tag® and TMT® are registered Trademarks of Proteome Sciences plc." RELATED []
-xref: record_id "984"
-xref: delta_mono_mass "299.166748"
-xref: delta_avge_mass "299.4322"
-xref: delta_composition "H(25) C(14) N(3) O(2) S"
-xref: username_of_poster "jorogers6"
-xref: group_of_poster ""
-xref: date_time_posted "2010-04-22 21:57:44"
-xref: date_time_modified "2024-08-12 10:07:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:985
-name: cysTMT6plex
-def: "Cysteine-reactive Sixplex Tandem Mass Tag®." [URL:http\://bit.ly/1GBnaC8, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=985]
-comment: This modification describes the isobaric sixplex cysteine-reactive cysTMT6 Reagents with isotopic labels. Upon CID, these reagents release reporter ions of 126.127725, 127.131079, 128.134433, 129.137787, 130.141141, and 131.138176 (monoisotopic mass).
-synonym: "Tandem Mass Tag® and TMT® are registered Trademarks of Proteome Sciences plc." RELATED []
-xref: record_id "985"
-xref: delta_mono_mass "304.177202"
-xref: delta_avge_mass "304.3962"
-xref: delta_composition "H(25) C(10) 13C(4) N(2) 15N O(2) S"
-xref: username_of_poster "jorogers6"
-xref: group_of_poster ""
-xref: date_time_posted "2010-04-22 22:05:46"
-xref: date_time_modified "2024-08-12 10:07:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:986
-name: Label:13C(6)+Dimethyl
-def: "Dimethyl 13C(6) Silac label." [FindMod:DIMETH, URL:http\://www.pil.sdu.dk/silac_intro.htm, PMID:http://www.ncbi.nlm.nih.gov/pubmed/14670044?dopt=AbstractPlus, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=986]
-xref: record_id "986"
-xref: delta_mono_mass "34.051429"
-xref: delta_avge_mass "34.0091"
-xref: delta_composition "H(4) C(-4) 13C(6)"
-xref: username_of_poster "glick2"
-xref: group_of_poster ""
-xref: date_time_posted "2010-05-09 10:48:19"
-xref: date_time_modified "2010-05-14 16:19:43"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "SILAC+PTM"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:987
-name: Label:13C(6)15N(2)+Dimethyl
-def: "Dimethyl 13C(6)15N(2) Silac label." [URL:http\://www.pil.sdu.dk/silac_intro.htm, FindMod:DIMETH, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=987]
-xref: record_id "987"
-xref: delta_mono_mass "36.045499"
-xref: delta_avge_mass "35.9959"
-xref: delta_composition "H(4) C(-4) 13C(6) N(-2) 15N(2)"
-xref: username_of_poster "glick2"
-xref: group_of_poster ""
-xref: date_time_posted "2010-05-09 10:57:55"
-xref: date_time_modified "2010-05-14 16:20:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_1_misc_notes "SILAC+PTM"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:989
-name: Ammonium
-def: "Replacement of proton with ammonium ion." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=989]
-comment: Sometimes observed after elution of phosphopeptides from TiO2 with ammonium hydroxide.
-xref: record_id "989"
-xref: delta_mono_mass "17.026549"
-xref: delta_avge_mass "17.0305"
-xref: delta_composition "H(3) N"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2010-05-18 10:32:03"
-xref: date_time_modified "2010-06-04 15:08:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Any C-term"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "E"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "D"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:991
-name: ISD_z+2_ion
-def: "ISD (z+2)-series." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=991]
-xref: record_id "991"
-xref: delta_mono_mass "-15.010899"
-xref: delta_avge_mass "-15.0146"
-xref: delta_composition "H(-1) N(-1)"
-xref: username_of_poster "suckau"
-xref: group_of_poster ""
-xref: date_time_posted "2010-06-08 09:42:52"
-xref: date_time_modified "2024-08-12 11:27:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Artefact"
-xref: spec_1_misc_notes "this is a virtual modification, as it only accounts for the structure of the MS/MS fragment as it occurs in Top-Down MS/MS analyses. This must be accounted for in MS³-analysis of z+2 ions"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:993
-name: Biotin:Sigma-B1267
-def: "Was Biotin-maleimide." [PMID:15449375, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=993]
-synonym: "maleimide biotinylated" RELATED []
-xref: record_id "993"
-xref: delta_mono_mass "449.17329"
-xref: delta_avge_mass "449.5239"
-xref: delta_composition "H(27) C(20) N(5) O(5) S"
-xref: username_of_poster "mpcusack"
-xref: group_of_poster ""
-xref: date_time_posted "2010-06-10 07:50:00"
-xref: date_time_modified "2010-12-03 16:02:22"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:994
-name: Label:15N(1)
-def: "15N(1)." [PMID:19664813, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=994]
-synonym: "Metabolic labeling with ammonium sulfate (15N)" RELATED []
-xref: record_id "994"
-xref: delta_mono_mass "0.997035"
-xref: delta_avge_mass "0.9934"
-xref: delta_composition "N(-1) 15N"
-xref: username_of_poster "ppicotti"
-xref: group_of_poster ""
-xref: date_time_posted "2010-06-22 14:52:08"
-xref: date_time_modified "2011-11-21 14:26:07"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "Y"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "G"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "A"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "S"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Isotopic label"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "P"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Isotopic label"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "V"
-xref: spec_7_position "Anywhere"
-xref: spec_7_classification "Isotopic label"
-xref: spec_8_group "8"
-xref: spec_8_hidden "1"
-xref: spec_8_site "T"
-xref: spec_8_position "Anywhere"
-xref: spec_8_classification "Isotopic label"
-xref: spec_9_group "9"
-xref: spec_9_hidden "1"
-xref: spec_9_site "C"
-xref: spec_9_position "Anywhere"
-xref: spec_9_classification "Isotopic label"
-xref: spec_10_group "10"
-xref: spec_10_hidden "1"
-xref: spec_10_site "I"
-xref: spec_10_position "Anywhere"
-xref: spec_10_classification "Isotopic label"
-xref: spec_11_group "11"
-xref: spec_11_hidden "1"
-xref: spec_11_site "L"
-xref: spec_11_position "Anywhere"
-xref: spec_11_classification "Isotopic label"
-xref: spec_12_group "12"
-xref: spec_12_hidden "1"
-xref: spec_12_site "D"
-xref: spec_12_position "Anywhere"
-xref: spec_12_classification "Isotopic label"
-xref: spec_13_group "13"
-xref: spec_13_hidden "1"
-xref: spec_13_site "E"
-xref: spec_13_position "Anywhere"
-xref: spec_13_classification "Isotopic label"
-xref: spec_14_group "14"
-xref: spec_14_hidden "1"
-xref: spec_14_site "M"
-xref: spec_14_position "Anywhere"
-xref: spec_14_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:995
-name: Label:15N(2)
-def: "15N(2)." [PMID:19664813, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=995]
-synonym: "Metabolic labeling with ammonium sulfate (15N)" RELATED []
-xref: record_id "995"
-xref: delta_mono_mass "1.99407"
-xref: delta_avge_mass "1.9868"
-xref: delta_composition "N(-2) 15N(2)"
-xref: username_of_poster "ppicotti"
-xref: group_of_poster ""
-xref: date_time_posted "2010-06-22 15:29:02"
-xref: date_time_modified "2011-11-21 14:26:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "Q"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "W"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:996
-name: Label:15N(3)
-def: "15N(3)." [PMID:19664813, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=996]
-synonym: "Metabolic labeling with ammonium sulfate (15N)" RELATED []
-xref: record_id "996"
-xref: delta_mono_mass "2.991105"
-xref: delta_avge_mass "2.9802"
-xref: delta_composition "N(-3) 15N(3)"
-xref: username_of_poster "ppicotti"
-xref: group_of_poster ""
-xref: date_time_posted "2010-06-22 15:30:28"
-xref: date_time_modified "2011-11-21 14:26:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:997
-name: sulfo+amino
-def: "Aminotyrosine with sulfation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=997]
-synonym: "amino_sulfate" RELATED []
-xref: record_id "997"
-xref: delta_mono_mass "94.967714"
-xref: delta_avge_mass "95.0778"
-xref: delta_composition "H N O(3) S"
-xref: username_of_poster "huidouzi"
-xref: group_of_poster ""
-xref: date_time_posted "2010-06-23 18:50:14"
-xref: date_time_modified "2010-06-28 10:29:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1000
-name: AHA-Alkyne
-def: "Azidohomoalanine (AHA) bound to propargylglycine-NH2 (alkyne)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1000]
-comment: Methionine (C5H11NO2S) is substituted in culture with azidohomoalanine (AHA - C4H8N4O2). The azide group reacts with the alkyne group propargylglycine-NH2. As a result the side chain of methionine (C3H7S) is substituted by C7H12N5O.
-xref: record_id "1000"
-xref: delta_mono_mass "107.077339"
-xref: delta_avge_mass "107.0504"
-xref: delta_composition "H(5) C(4) N(5) O S(-1)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2010-09-28 09:28:15"
-xref: date_time_modified "2010-10-03 13:44:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1001
-name: AHA-Alkyne-KDDDD
-def: "Azidohomoalanine (AHA) bound to DDDDK-propargylglycine-NH2 (alkyne)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1001]
-comment: Methionine (C5H11NO2S) is substituted in culture with azidohomoalanine (AHA - C4H8N4O2). The azide group reacts with the alkyne group DDDDK-propargylglycine-NH2. As a result the side chain of methionine (C3H7S) is substituted by C29H44N11O14.
-xref: record_id "1001"
-xref: delta_mono_mass "695.280074"
-xref: delta_avge_mass "695.5723"
-xref: delta_composition "H(37) C(26) N(11) O(14) S(-1)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2010-09-28 09:35:48"
-xref: date_time_modified "2010-10-03 13:44:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1002
-name: EGCG1
-def: "(-)-epigallocatechin-3-gallate." [PMID:18771724, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1002]
-comment: Created for Bindu Abraham 2010-10-05.
-xref: record_id "1002"
-xref: delta_mono_mass "456.069261"
-xref: delta_avge_mass "456.3558"
-xref: delta_composition "H(16) C(22) O(11)"
-xref: username_of_poster "hooverdm"
-xref: group_of_poster ""
-xref: date_time_posted "2010-10-05 20:46:40"
-xref: date_time_modified "2010-12-23 15:47:42"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1003
-name: EGCG2
-def: "(-)-dehydroepigallocatechin." [PMID:18771724, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1003]
-comment: Created for Bindu Abraham 2010-10-05.
-xref: record_id "1003"
-xref: delta_mono_mass "287.055563"
-xref: delta_avge_mass "287.2442"
-xref: delta_composition "H(11) C(15) O(6)"
-xref: username_of_poster "hooverdm"
-xref: group_of_poster ""
-xref: date_time_posted "2010-10-05 20:48:38"
-xref: date_time_modified "2010-12-23 15:47:33"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1004
-name: Label:13C(6)15N(4)+Methyl
-def: "Monomethylated Arg13C(6) 15N(4)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1004]
-xref: record_id "1004"
-xref: delta_mono_mass "24.023919"
-xref: delta_avge_mass "23.9561"
-xref: delta_composition "H(2) C(-5) 13C(6) N(-4) 15N(4)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2010-10-27 10:36:31"
-xref: date_time_modified "2010-11-05 16:47:36"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1005
-name: Label:13C(6)15N(4)+Dimethyl
-def: "Dimethylated Arg13C(6) 15N(4)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1005]
-xref: record_id "1005"
-xref: delta_mono_mass "38.039569"
-xref: delta_avge_mass "37.9827"
-xref: delta_composition "H(4) C(-4) 13C(6) N(-4) 15N(4)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2010-10-27 10:52:10"
-xref: date_time_modified "2010-11-05 16:49:29"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1006
-name: Label:13C(6)15N(4)+Methyl:2H(3)13C(1)
-def: "2H(3) 13C(1) monomethylated Arg13C(6) 15N(4)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1006]
-xref: record_id "1006"
-xref: delta_mono_mass "28.046104"
-xref: delta_avge_mass "27.9673"
-xref: delta_composition "H(-1) 2H(3) C(-6) 13C(7) N(-4) 15N(4)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2010-10-27 10:59:21"
-xref: date_time_modified "2010-11-05 16:53:21"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1007
-name: Label:13C(6)15N(4)+Dimethyl:2H(6)13C(2)
-def: "2H(6) 13C(2) Dimethylated Arg13C(6) 15N(4)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1007]
-xref: record_id "1007"
-xref: delta_mono_mass "46.083939"
-xref: delta_avge_mass "46.005"
-xref: delta_composition "H(-2) 2H(6) C(-6) 13C(8) N(-4) 15N(4)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2010-10-27 11:07:29"
-xref: date_time_modified "2010-11-05 16:54:24"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1008
-name: Cys->CamSec
-def: "Sec Iodoacetamide derivative." [PMID:18283440, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1008]
-synonym: "Carboxyamidomethylation of selenocysteine" RELATED []
-xref: record_id "1008"
-xref: delta_mono_mass "104.965913"
-xref: delta_avge_mass "103.9463"
-xref: delta_composition "H(3) C(2) N O S(-1) Se"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2010-11-04 12:00:12"
-xref: date_time_modified "2016-02-01 14:19:53"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Non-standard residue"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1009
-name: Thiazolidine
-def: "Formaldehyde adduct." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1009]
-synonym: "thiazolidine-2-carboxylic acid" RELATED []
-xref: record_id "1009"
-xref: delta_mono_mass "12"
-xref: delta_avge_mass "12.0107"
-xref: delta_composition "C"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2010-11-04 12:29:10"
-xref: date_time_modified "2017-03-30 16:37:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "R"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "H"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "Y"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "W"
-xref: spec_7_position "Anywhere"
-xref: spec_7_classification "Chemical derivative"
-xref: spec_8_group "8"
-xref: spec_8_hidden "1"
-xref: spec_8_site "F"
-xref: spec_8_position "Anywhere"
-xref: spec_8_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1010
-name: DEDGFLYMVYASQETFG
-def: "Addition of DEDGFLYMVYASQETFG." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1010]
-xref: record_id "1010"
-xref: delta_mono_mass "1970.824411"
-xref: delta_avge_mass "1972.088"
-xref: delta_composition "H(122) C(89) N(18) O(31) S"
-xref: username_of_poster "hbromage"
-xref: group_of_poster ""
-xref: date_time_posted "2010-11-04 17:27:46"
-xref: date_time_modified "2010-11-24 18:00:09"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_1_neutral_loss_19_mono_mass "18.010565"
-xref: spec_1_neutral_loss_19_avge_mass "18.0153"
-xref: spec_1_neutral_loss_19_flag "false"
-xref: spec_1_neutral_loss_19_composition "Water"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1012
-name: Biotin:Invitrogen-M1602
-def: "Nalpha-(3-maleimidylpropionyl)biocytin." [URL:http\://products.invitrogen.com/ivgn/product/M1602?ICID=search-m1602, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1012]
-synonym: "Reference M1602 Invitrogen" RELATED []
-xref: record_id "1012"
-xref: delta_mono_mass "523.210069"
-xref: delta_avge_mass "523.6024"
-xref: delta_composition "H(33) C(23) N(5) O(7) S"
-xref: username_of_poster "camoin"
-xref: group_of_poster ""
-xref: date_time_posted "2010-11-16 10:11:53"
-xref: date_time_modified "2010-12-03 15:58:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1014
-name: glycidamide
-def: "Glycidamide adduct." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1014]
-xref: record_id "1014"
-xref: delta_mono_mass "87.032028"
-xref: delta_avge_mass "87.0773"
-xref: delta_composition "H(5) C(3) N O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2010-12-21 17:00:41"
-xref: date_time_modified "2024-08-12 09:49:53"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1015
-name: Ahx2+Hsl
-def: "C-terminal homoserine lactone and two aminohexanoic acids." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1015]
-xref: record_id "1015"
-xref: delta_mono_mass "309.205242"
-xref: delta_avge_mass "309.4039"
-xref: delta_composition "H(27) C(16) N(3) O(3)"
-xref: username_of_poster "kpkent"
-xref: group_of_poster ""
-xref: date_time_posted "2010-12-22 10:13:01"
-xref: date_time_modified "2011-01-07 17:06:08"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Any C-term"
-xref: spec_1_classification "Non-standard residue"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1017
-name: DMPO
-def: "DMPO spin-trap nitrone adduct." [PMID:18160050, PMID:17637042, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1017]
-comment: Created for Bindu Abraham 2011-01-25.
-xref: record_id "1017"
-xref: delta_mono_mass "111.068414"
-xref: delta_avge_mass "111.1418"
-xref: delta_composition "H(9) C(6) N O"
-xref: username_of_poster "hooverdm"
-xref: group_of_poster ""
-xref: date_time_posted "2011-01-25 18:30:32"
-xref: date_time_modified "2011-02-28 17:17:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1018
-name: ICDID
-def: "Isotope-Coded Dimedone light form." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1018]
-xref: record_id "1018"
-xref: delta_mono_mass "138.06808"
-xref: delta_avge_mass "138.1638"
-xref: delta_composition "H(10) C(8) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-02-02 17:23:34"
-xref: date_time_modified "2011-02-02 17:23:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1019
-name: ICDID:2H(6)
-def: "Isotope-Coded Dimedone heavy form." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1019]
-xref: record_id "1019"
-xref: delta_mono_mass "144.10574"
-xref: delta_avge_mass "144.2008"
-xref: delta_composition "H(4) 2H(6) C(8) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-02-02 17:24:45"
-xref: date_time_modified "2011-02-02 17:24:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1020
-name: Xlink:DSS[156]
-def: "Water-quenched monolink of DSS/BS3 crosslinker." [PMID:8326953, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1020]
-xref: record_id "1020"
-xref: delta_mono_mass "156.078644"
-xref: delta_avge_mass "156.1791"
-xref: delta_composition "H(12) C(8) O(3)"
-xref: username_of_poster "Kramerh"
-xref: group_of_poster ""
-xref: date_time_posted "2011-02-07 14:20:22"
-xref: date_time_modified "2017-08-17 15:09:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1021
-name: Xlink:EGS[244]
-def: "Water quenched monolink of EGS cross-linker." [PMID:36892, URL:https\://tools.thermofisher.com/content/sfs/manuals/MAN0011281_EGS_SulfoEGS_UG.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1021]
-synonym: "Ethylene glycolbis(succinimidylsuccinate)" RELATED []
-xref: record_id "1021"
-xref: delta_mono_mass "244.058303"
-xref: delta_avge_mass "244.1981"
-xref: delta_composition "H(12) C(10) O(7)"
-xref: username_of_poster "Kramerh"
-xref: group_of_poster ""
-xref: date_time_posted "2011-02-07 17:40:36"
-xref: date_time_modified "2017-08-17 15:10:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1022
-name: Xlink:DST[132]
-def: "Water quenched monolink of DST crosslinker." [PMID:212103, URL:https\://assets.thermofisher.com/TFS-Assets/LSG/manuals/MAN0011282_DST_UG.pdf, PMID:3001048, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1022]
-xref: record_id "1022"
-xref: delta_mono_mass "132.005873"
-xref: delta_avge_mass "132.0716"
-xref: delta_composition "H(4) C(4) O(5)"
-xref: username_of_poster "Kramerh"
-xref: group_of_poster ""
-xref: date_time_posted "2011-02-07 18:02:58"
-xref: date_time_modified "2017-08-18 14:26:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1023
-name: Xlink:DTSSP[192]
-def: "Water quenched monolink of DSP/DTSSP crosslinker." [URL:https\://tools.thermofisher.com/content/sfs/manuals/MAN0011280_DTSSP_DSP_UG.pdf, PMID:1262347, PMID:8457554, PMID:322714, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1023]
-synonym: "Also known as DSP" RELATED []
-xref: record_id "1023"
-xref: delta_mono_mass "191.991486"
-xref: delta_avge_mass "192.2559"
-xref: delta_composition "H(8) C(6) O(3) S(2)"
-xref: username_of_poster "Kramerh"
-xref: group_of_poster ""
-xref: date_time_posted "2011-02-07 18:22:31"
-xref: date_time_modified "2017-08-18 14:53:07"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1024
-name: Xlink:SMCC[237]
-def: "Water quenched monolink of SMCC." [PMID:6490581, PMID:1931231, URL:https\://assets.thermofisher.com/TFS-Assets/LSG/manuals/MAN0011295_SMCC_SulfoSMCC_UG.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1024]
-xref: record_id "1024"
-xref: delta_mono_mass "237.100108"
-xref: delta_avge_mass "237.2518"
-xref: delta_composition "H(15) C(12) N O(4)"
-xref: username_of_poster "Kramerh"
-xref: group_of_poster ""
-xref: date_time_posted "2011-02-07 19:33:39"
-xref: date_time_modified "2017-09-05 15:09:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1027
-name: Xlink:DMP[140]
-def: "Water quenched monolink of DMP crosslinker." [PMID:2144419, PMID:14696200, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1027]
-synonym: "Dimethyl pimelimidate dead-end crosslink" RELATED []
-xref: record_id "1027"
-xref: delta_mono_mass "140.094963"
-xref: delta_avge_mass "140.183"
-xref: delta_composition "H(12) C(7) N(2) O"
-xref: username_of_poster "Kramerh"
-xref: group_of_poster ""
-xref: date_time_posted "2011-02-25 16:18:13"
-xref: date_time_modified "2017-08-18 10:17:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1028
-name: Xlink:EGS[115]
-def: "Cleavage product of EGS protein crosslinks by hydroylamine treatment." [PMID:36892, URL:https\://tools.thermofisher.com/content/sfs/manuals/MAN0011281_EGS_SulfoEGS_UG.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1028]
-synonym: "Ethylene glycolbis(succinimidylsuccinate)" RELATED []
-xref: record_id "1028"
-xref: delta_mono_mass "115.026943"
-xref: delta_avge_mass "115.0874"
-xref: delta_composition "H(5) C(4) N O(3)"
-xref: username_of_poster "Kramerh"
-xref: group_of_poster ""
-xref: date_time_posted "2011-02-25 17:16:45"
-xref: date_time_modified "2017-08-17 15:10:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1031
-name: Biotin:Thermo-88310
-def: "Desthiobiotin modification of lysine." [URL:http\://www.lifetechnologies.com/order/catalog/product/88310, URL:http\://www.lifetechnologies.com/order/catalog/product/88314, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1031]
-synonym: "desthiobiotin-GTP desthiobiotin-ADP desthiobiotin-ATP" RELATED []
-xref: record_id "1031"
-xref: delta_mono_mass "196.121178"
-xref: delta_avge_mass "196.2462"
-xref: delta_composition "H(16) C(10) N(2) O(2)"
-xref: username_of_poster "rbomgard"
-xref: group_of_poster ""
-xref: date_time_posted "2011-03-02 20:33:20"
-xref: date_time_modified "2015-04-20 16:11:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1032
-name: 2-nitrobenzyl
-def: "Tyrosine caged with 2-nitrobenzyl (ONB)." [PMID:16548032, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1032]
-xref: record_id "1032"
-xref: delta_mono_mass "135.032028"
-xref: delta_avge_mass "135.1201"
-xref: delta_composition "H(5) C(7) N O(2)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2011-03-14 10:56:33"
-xref: date_time_modified "2011-03-18 13:39:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1033
-name: Cys->SecNEM
-def: "N-ethylmaleimide on selenocysteines." [URL:http\://www.chemistry.ucsc.edu/~fink/231/Image118.gif, PMID:18283440, PMID:12777388, PMID:11813307, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1033]
-synonym: "SecNEM" RELATED []
-xref: record_id "1033"
-xref: delta_mono_mass "172.992127"
-xref: delta_avge_mass "172.0203"
-xref: delta_composition "H(7) C(6) N O(2) S(-1) Se"
-xref: username_of_poster "mpcusack"
-xref: group_of_poster ""
-xref: date_time_posted "2011-03-31 18:29:45"
-xref: date_time_modified "2016-02-01 14:20:14"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Non-standard residue"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1034
-name: Cys->SecNEM:2H(5)
-def: "D5 N-ethylmaleimide on selenocysteines." [PMID:18283440, PMID:12777388, URL:http\://www.chemistry.ucsc.edu/~fink/231/Image118.gif, PMID:11813307, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1034]
-synonym: "SecNEM D5" RELATED []
-xref: record_id "1034"
-xref: delta_mono_mass "178.023511"
-xref: delta_avge_mass "177.0511"
-xref: delta_composition "H(2) 2H(5) C(6) N O(2) S(-1) Se"
-xref: username_of_poster "mpcusack"
-xref: group_of_poster ""
-xref: date_time_posted "2011-03-31 18:32:32"
-xref: date_time_modified "2016-02-01 14:20:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1035
-name: Thiadiazole
-def: "Thiadiazolydation of Cys." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1035]
-xref: record_id "1035"
-xref: delta_mono_mass "174.025169"
-xref: delta_avge_mass "174.2223"
-xref: delta_composition "H(6) C(9) N(2) S"
-xref: username_of_poster "cbatthya"
-xref: group_of_poster ""
-xref: date_time_posted "2011-04-01 16:26:52"
-xref: date_time_modified "2011-04-08 16:38:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1036
-name: Withaferin
-def: "Modification of cystein by withaferin." [PMID:http://www.ncbi.nlm.nih.gov/pubmed/21432907, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1036]
-xref: record_id "1036"
-xref: delta_mono_mass "470.266839"
-xref: delta_avge_mass "470.5977"
-xref: delta_composition "H(38) C(28) O(6)"
-xref: username_of_poster "ProtUA"
-xref: group_of_poster ""
-xref: date_time_posted "2011-04-06 12:31:40"
-xref: date_time_modified "2011-04-08 16:37:15"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1037
-name: Biotin:Thermo-88317
-def: "Desthiobiotin fluorophosphonate." [URL:http\://www.lifetechnologies.com/order/catalog/product/88317, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1037]
-comment: Dethiobiotin-FP was designed to label the active site serine of serine hydrolases (e.g. esterases, peptidases, lipases).
-synonym: "desthiobiotin-alkyl-FP desthiobiotin-FP" RELATED []
-xref: record_id "1037"
-xref: delta_mono_mass "443.291294"
-xref: delta_avge_mass "443.5603"
-xref: delta_composition "H(42) C(22) N(3) O(4) P"
-xref: username_of_poster "rbomgard"
-xref: group_of_poster ""
-xref: date_time_posted "2011-05-06 19:40:48"
-xref: date_time_modified "2015-04-20 16:24:29"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1038
-name: TAMRA-FP
-def: "TAMRA fluorophosphonate modification of serine." [URL:http\://www.piercenet.com/browse.cfm?fldID=0842EF3A-D867-AEA2-6E77-E84116CAA87C, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1038]
-comment: TAMRA-FP was designed to label the active site serine of serine hydrolases (e.g. esterases, peptidases, lipases).
-synonym: "ActivX TAMRA-FP Serine Hydrolase Probe TAMRA-alkyl-FP" RELATED []
-xref: record_id "1038"
-xref: delta_mono_mass "659.312423"
-xref: delta_avge_mass "659.7514"
-xref: delta_composition "H(46) C(37) N(3) O(6) P"
-xref: username_of_poster "rbomgard"
-xref: group_of_poster ""
-xref: date_time_posted "2011-05-06 20:03:27"
-xref: date_time_modified "2011-05-09 16:01:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "Y"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1039
-name: Biotin:Thermo-21901+H2O
-def: "Maleimide-Biotin + Water." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1039]
-synonym: "Maleimide-PEG2-Biotin + Water" RELATED []
-xref: record_id "1039"
-xref: delta_mono_mass "543.236284"
-xref: delta_avge_mass "543.6336"
-xref: delta_composition "H(37) C(23) N(5) O(8) S"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2011-05-18 16:28:42"
-xref: date_time_modified "2011-05-25 16:02:07"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1041
-name: Deoxyhypusine
-def: "Deoxyhypusine." [PMID:20942800, PMID:10542236, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1041]
-comment: Deoxyhypusine synthase catalyzes the formation of a deoxyhypusine by transferring an aminobutyl moiety from spermidine onto a conserved lysine residue within the eIF5A.
-xref: record_id "1041"
-xref: delta_mono_mass "71.073499"
-xref: delta_avge_mass "71.121"
-xref: delta_composition "H(9) C(4) N"
-xref: username_of_poster "cbarrero"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-15 12:04:35"
-xref: date_time_modified "2024-08-12 10:11:43"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "Q"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_2_misc_notes "putrescine Q-PUT"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1042
-name: Acetyldeoxyhypusine
-def: "Acetyldeoxyhypusine." [PMID:20942800, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1042]
-comment: Regulation of eIF5A by deoxyhypusine acetylation/deacetylation.
-xref: record_id "1042"
-xref: delta_mono_mass "113.084064"
-xref: delta_avge_mass "113.1576"
-xref: delta_composition "H(11) C(6) N O"
-xref: username_of_poster "cbarrero"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-18 04:14:19"
-xref: date_time_modified "2021-07-06 14:44:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1043
-name: Acetylhypusine
-def: "Acetylhypusine." [PMID:20942800, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1043]
-comment: Regulation of eIF5A by hypusine acetylation/deacetylation.
-xref: record_id "1043"
-xref: delta_mono_mass "129.078979"
-xref: delta_avge_mass "129.157"
-xref: delta_composition "H(11) C(6) N O(2)"
-xref: username_of_poster "cbarrero"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-18 04:16:59"
-xref: date_time_modified "2021-07-06 14:44:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1044
-name: Ala->Cys
-def: "Ala->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1044]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1044"
-xref: delta_mono_mass "31.972071"
-xref: delta_avge_mass "32.065"
-xref: delta_composition "S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 16:49:30"
-xref: date_time_modified "2011-06-20 16:49:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1045
-name: Ala->Phe
-def: "Ala->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1045]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1045"
-xref: delta_mono_mass "76.0313"
-xref: delta_avge_mass "76.096"
-xref: delta_composition "H(4) C(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 16:50:25"
-xref: date_time_modified "2011-06-20 16:50:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1046
-name: Ala->His
-def: "Ala->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1046]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1046"
-xref: delta_mono_mass "66.021798"
-xref: delta_avge_mass "66.0614"
-xref: delta_composition "H(2) C(3) N(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 16:56:21"
-xref: date_time_modified "2011-06-20 16:56:21"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1047
-name: Ala->Xle
-def: "Ala->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1047]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1047"
-xref: delta_mono_mass "42.04695"
-xref: delta_avge_mass "42.0797"
-xref: delta_composition "H(6) C(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 16:57:10"
-xref: date_time_modified "2011-06-21 15:12:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1048
-name: Ala->Lys
-def: "Ala->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1048]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1048"
-xref: delta_mono_mass "57.057849"
-xref: delta_avge_mass "57.0944"
-xref: delta_composition "H(7) C(3) N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 16:57:37"
-xref: date_time_modified "2011-06-20 16:57:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1049
-name: Ala->Met
-def: "Ala->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1049]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1049"
-xref: delta_mono_mass "60.003371"
-xref: delta_avge_mass "60.1182"
-xref: delta_composition "H(4) C(2) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 16:58:05"
-xref: date_time_modified "2011-06-20 16:58:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1050
-name: Ala->Asn
-def: "Ala->Asn substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1050]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1050"
-xref: delta_mono_mass "43.005814"
-xref: delta_avge_mass "43.0247"
-xref: delta_composition "H C N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 16:58:32"
-xref: date_time_modified "2011-06-20 16:58:32"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1051
-name: Ala->Gln
-def: "Ala->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1051]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1051"
-xref: delta_mono_mass "57.021464"
-xref: delta_avge_mass "57.0513"
-xref: delta_composition "H(3) C(2) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 16:58:56"
-xref: date_time_modified "2011-06-20 16:58:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1052
-name: Ala->Arg
-def: "Ala->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1052]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1052"
-xref: delta_mono_mass "85.063997"
-xref: delta_avge_mass "85.1078"
-xref: delta_composition "H(7) C(3) N(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 16:59:22"
-xref: date_time_modified "2011-06-20 16:59:22"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1053
-name: Ala->Trp
-def: "Ala->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1053]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1053"
-xref: delta_mono_mass "115.042199"
-xref: delta_avge_mass "115.132"
-xref: delta_composition "H(5) C(8) N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 16:59:45"
-xref: date_time_modified "2011-06-20 16:59:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1054
-name: Ala->Tyr
-def: "Ala->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1054]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1054"
-xref: delta_mono_mass "92.026215"
-xref: delta_avge_mass "92.0954"
-xref: delta_composition "H(4) C(6) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:00:09"
-xref: date_time_modified "2011-06-20 17:00:09"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1055
-name: Cys->Ala
-def: "Cys->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1055]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1055"
-xref: delta_mono_mass "-31.972071"
-xref: delta_avge_mass "-32.065"
-xref: delta_composition "S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:26:22"
-xref: date_time_modified "2011-06-20 17:26:22"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1056
-name: Cys->Asp
-def: "Cys->Asp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1056]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1056"
-xref: delta_mono_mass "12.017759"
-xref: delta_avge_mass "11.9445"
-xref: delta_composition "C O(2) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:26:57"
-xref: date_time_modified "2011-06-20 17:26:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1057
-name: Cys->Glu
-def: "Cys->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1057]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1057"
-xref: delta_mono_mass "26.033409"
-xref: delta_avge_mass "25.9711"
-xref: delta_composition "H(2) C(2) O(2) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:27:25"
-xref: date_time_modified "2011-06-20 17:27:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1058
-name: Cys->His
-def: "Cys->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1058]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1058"
-xref: delta_mono_mass "34.049727"
-xref: delta_avge_mass "33.9964"
-xref: delta_composition "H(2) C(3) N(2) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:27:48"
-xref: date_time_modified "2011-06-20 17:27:48"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1059
-name: Cys->Xle
-def: "Cys->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1059]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1059"
-xref: delta_mono_mass "10.07488"
-xref: delta_avge_mass "10.0147"
-xref: delta_composition "H(6) C(3) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:28:11"
-xref: date_time_modified "2011-06-21 15:14:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1060
-name: Cys->Lys
-def: "Cys->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1060]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1060"
-xref: delta_mono_mass "25.085779"
-xref: delta_avge_mass "25.0294"
-xref: delta_composition "H(7) C(3) N S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:28:36"
-xref: date_time_modified "2011-06-20 17:28:36"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1061
-name: Cys->Met
-def: "Cys->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1061]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1061"
-xref: delta_mono_mass "28.0313"
-xref: delta_avge_mass "28.0532"
-xref: delta_composition "H(4) C(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:29:04"
-xref: date_time_modified "2011-06-20 17:29:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1062
-name: Cys->Asn
-def: "Cys->Asn substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1062]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1062"
-xref: delta_mono_mass "11.033743"
-xref: delta_avge_mass "10.9597"
-xref: delta_composition "H C N O S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:29:28"
-xref: date_time_modified "2011-06-20 17:29:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1063
-name: Cys->Pro
-def: "Cys->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1063]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1063"
-xref: delta_mono_mass "-5.956421"
-xref: delta_avge_mass "-6.0277"
-xref: delta_composition "H(2) C(2) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:29:55"
-xref: date_time_modified "2011-06-20 17:29:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1064
-name: Cys->Gln
-def: "Cys->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1064]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1064"
-xref: delta_mono_mass "25.049393"
-xref: delta_avge_mass "24.9863"
-xref: delta_composition "H(3) C(2) N O S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:30:19"
-xref: date_time_modified "2011-06-20 17:30:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1065
-name: Cys->Thr
-def: "Cys->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1065]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1065"
-xref: delta_mono_mass "-1.961506"
-xref: delta_avge_mass "-2.039"
-xref: delta_composition "H(2) C O S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:30:53"
-xref: date_time_modified "2011-06-20 17:30:53"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1066
-name: Cys->Val
-def: "Cys->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1066]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1066"
-xref: delta_mono_mass "-3.940771"
-xref: delta_avge_mass "-4.0118"
-xref: delta_composition "H(4) C(2) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:31:23"
-xref: date_time_modified "2011-06-20 17:31:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1067
-name: Asp->Cys
-def: "Asp->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1067]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1067"
-xref: delta_mono_mass "-12.017759"
-xref: delta_avge_mass "-11.9445"
-xref: delta_composition "C(-1) O(-2) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:40:11"
-xref: date_time_modified "2011-06-20 17:40:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1068
-name: Asp->Phe
-def: "Asp->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1068]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1068"
-xref: delta_mono_mass "32.041471"
-xref: delta_avge_mass "32.0865"
-xref: delta_composition "H(4) C(5) O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:40:35"
-xref: date_time_modified "2011-06-20 17:40:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1069
-name: Asp->Xle
-def: "Asp->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1069]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1069"
-xref: delta_mono_mass "-1.942879"
-xref: delta_avge_mass "-1.9298"
-xref: delta_composition "H(6) C(2) O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:41:00"
-xref: date_time_modified "2011-06-21 15:14:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1070
-name: Asp->Lys
-def: "Asp->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1070]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1070"
-xref: delta_mono_mass "13.06802"
-xref: delta_avge_mass "13.0849"
-xref: delta_composition "H(7) C(2) N O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:41:26"
-xref: date_time_modified "2011-06-20 17:41:26"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1071
-name: Asp->Met
-def: "Asp->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1071]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1071"
-xref: delta_mono_mass "16.013542"
-xref: delta_avge_mass "16.1087"
-xref: delta_composition "H(4) C O(-2) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:41:51"
-xref: date_time_modified "2011-06-20 17:41:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1072
-name: Asp->Pro
-def: "Asp->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1072]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1072"
-xref: delta_mono_mass "-17.974179"
-xref: delta_avge_mass "-17.9722"
-xref: delta_composition "H(2) C O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:42:17"
-xref: date_time_modified "2011-06-20 17:42:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1073
-name: Asp->Gln
-def: "Asp->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1073]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1073"
-xref: delta_mono_mass "13.031634"
-xref: delta_avge_mass "13.0418"
-xref: delta_composition "H(3) C N O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:42:41"
-xref: date_time_modified "2011-06-20 17:42:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1074
-name: Asp->Arg
-def: "Asp->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1074]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1074"
-xref: delta_mono_mass "41.074168"
-xref: delta_avge_mass "41.0983"
-xref: delta_composition "H(7) C(2) N(3) O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:43:03"
-xref: date_time_modified "2011-06-20 17:43:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1075
-name: Asp->Ser
-def: "Asp->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1075]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1075"
-xref: delta_mono_mass "-27.994915"
-xref: delta_avge_mass "-28.0101"
-xref: delta_composition "C(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:43:25"
-xref: date_time_modified "2011-06-20 17:43:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1076
-name: Asp->Thr
-def: "Asp->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1076]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1076"
-xref: delta_mono_mass "-13.979265"
-xref: delta_avge_mass "-13.9835"
-xref: delta_composition "H(2) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:43:51"
-xref: date_time_modified "2011-06-20 17:43:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1077
-name: Asp->Trp
-def: "Asp->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1077]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1077"
-xref: delta_mono_mass "71.05237"
-xref: delta_avge_mass "71.1225"
-xref: delta_composition "H(5) C(7) N O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-20 17:44:16"
-xref: date_time_modified "2011-06-20 17:44:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1078
-name: Glu->Cys
-def: "Glu->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1078]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1078"
-xref: delta_mono_mass "-26.033409"
-xref: delta_avge_mass "-25.9711"
-xref: delta_composition "H(-2) C(-2) O(-2) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 12:00:46"
-xref: date_time_modified "2011-06-21 12:00:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1079
-name: Glu->Phe
-def: "Glu->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1079]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1079"
-xref: delta_mono_mass "18.025821"
-xref: delta_avge_mass "18.0599"
-xref: delta_composition "H(2) C(4) O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 12:01:12"
-xref: date_time_modified "2011-06-21 12:01:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1080
-name: Glu->His
-def: "Glu->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1080]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1080"
-xref: delta_mono_mass "8.016319"
-xref: delta_avge_mass "8.0253"
-xref: delta_composition "C N(2) O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 12:01:42"
-xref: date_time_modified "2011-06-21 12:01:42"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1081
-name: Glu->Xle
-def: "Glu->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1081]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1081"
-xref: delta_mono_mass "-15.958529"
-xref: delta_avge_mass "-15.9563"
-xref: delta_composition "H(4) C O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 12:02:09"
-xref: date_time_modified "2011-06-21 15:15:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1082
-name: Glu->Met
-def: "Glu->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1082]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1082"
-xref: delta_mono_mass "1.997892"
-xref: delta_avge_mass "2.0821"
-xref: delta_composition "H(2) O(-2) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 12:02:35"
-xref: date_time_modified "2011-06-21 12:02:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1083
-name: Glu->Asn
-def: "Glu->Asn substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1083]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1083"
-xref: delta_mono_mass "-14.999666"
-xref: delta_avge_mass "-15.0113"
-xref: delta_composition "H(-1) C(-1) N O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 12:03:01"
-xref: date_time_modified "2011-06-21 12:03:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1084
-name: Glu->Pro
-def: "Glu->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1084]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1084"
-xref: delta_mono_mass "-31.989829"
-xref: delta_avge_mass "-31.9988"
-xref: delta_composition "O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 12:03:25"
-xref: date_time_modified "2011-06-21 12:03:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1085
-name: Glu->Arg
-def: "Glu->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1085]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1085"
-xref: delta_mono_mass "27.058518"
-xref: delta_avge_mass "27.0717"
-xref: delta_composition "H(5) C N(3) O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 12:03:48"
-xref: date_time_modified "2011-06-21 12:03:48"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1086
-name: Glu->Ser
-def: "Glu->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1086]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1086"
-xref: delta_mono_mass "-42.010565"
-xref: delta_avge_mass "-42.0367"
-xref: delta_composition "H(-2) C(-2) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 12:04:12"
-xref: date_time_modified "2011-06-21 12:04:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1087
-name: Glu->Thr
-def: "Glu->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1087]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1087"
-xref: delta_mono_mass "-27.994915"
-xref: delta_avge_mass "-28.0101"
-xref: delta_composition "C(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 12:04:38"
-xref: date_time_modified "2011-06-21 12:04:38"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1088
-name: Glu->Trp
-def: "Glu->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1088]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1088"
-xref: delta_mono_mass "57.03672"
-xref: delta_avge_mass "57.0959"
-xref: delta_composition "H(3) C(6) N O(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 12:05:01"
-xref: date_time_modified "2011-06-21 12:05:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1089
-name: Glu->Tyr
-def: "Glu->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1089]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1089"
-xref: delta_mono_mass "34.020735"
-xref: delta_avge_mass "34.0593"
-xref: delta_composition "H(2) C(4) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 12:05:23"
-xref: date_time_modified "2011-06-21 12:05:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1090
-name: Phe->Ala
-def: "Phe->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1090]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1090"
-xref: delta_mono_mass "-76.0313"
-xref: delta_avge_mass "-76.096"
-xref: delta_composition "H(-4) C(-6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 13:41:15"
-xref: date_time_modified "2011-06-21 13:41:15"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1091
-name: Phe->Asp
-def: "Phe->Asp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1091]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1091"
-xref: delta_mono_mass "-32.041471"
-xref: delta_avge_mass "-32.0865"
-xref: delta_composition "H(-4) C(-5) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 13:41:48"
-xref: date_time_modified "2011-06-21 13:41:48"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1092
-name: Phe->Glu
-def: "Phe->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1092]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1092"
-xref: delta_mono_mass "-18.025821"
-xref: delta_avge_mass "-18.0599"
-xref: delta_composition "H(-2) C(-4) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 13:56:57"
-xref: date_time_modified "2011-06-21 13:56:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1093
-name: Phe->Gly
-def: "Phe->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1093]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1093"
-xref: delta_mono_mass "-90.04695"
-xref: delta_avge_mass "-90.1225"
-xref: delta_composition "H(-6) C(-7)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 13:57:23"
-xref: date_time_modified "2011-06-21 13:57:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1094
-name: Phe->His
-def: "Phe->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1094]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1094"
-xref: delta_mono_mass "-10.009502"
-xref: delta_avge_mass "-10.0346"
-xref: delta_composition "H(-2) C(-3) N(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 13:57:45"
-xref: date_time_modified "2011-06-21 13:57:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1095
-name: Phe->Lys
-def: "Phe->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1095]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1095"
-xref: delta_mono_mass "-18.973451"
-xref: delta_avge_mass "-19.0016"
-xref: delta_composition "H(3) C(-3) N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 13:58:10"
-xref: date_time_modified "2011-06-21 13:58:10"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1096
-name: Phe->Met
-def: "Phe->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1096]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1096"
-xref: delta_mono_mass "-16.027929"
-xref: delta_avge_mass "-15.9778"
-xref: delta_composition "C(-4) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 13:58:32"
-xref: date_time_modified "2011-06-21 13:58:32"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1097
-name: Phe->Asn
-def: "Phe->Asn substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1097]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1097"
-xref: delta_mono_mass "-33.025486"
-xref: delta_avge_mass "-33.0712"
-xref: delta_composition "H(-3) C(-5) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 13:58:57"
-xref: date_time_modified "2011-06-21 13:58:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1098
-name: Phe->Pro
-def: "Phe->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1098]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1098"
-xref: delta_mono_mass "-50.01565"
-xref: delta_avge_mass "-50.0587"
-xref: delta_composition "H(-2) C(-4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 13:59:19"
-xref: date_time_modified "2011-06-21 13:59:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1099
-name: Phe->Gln
-def: "Phe->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1099]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1099"
-xref: delta_mono_mass "-19.009836"
-xref: delta_avge_mass "-19.0446"
-xref: delta_composition "H(-1) C(-4) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 13:59:42"
-xref: date_time_modified "2011-06-21 13:59:42"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1100
-name: Phe->Arg
-def: "Phe->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1100]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1100"
-xref: delta_mono_mass "9.032697"
-xref: delta_avge_mass "9.0118"
-xref: delta_composition "H(3) C(-3) N(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:00:05"
-xref: date_time_modified "2011-06-21 14:00:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1101
-name: Phe->Thr
-def: "Phe->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1101]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1101"
-xref: delta_mono_mass "-46.020735"
-xref: delta_avge_mass "-46.07"
-xref: delta_composition "H(-2) C(-5) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:00:30"
-xref: date_time_modified "2011-06-21 14:00:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1102
-name: Phe->Trp
-def: "Phe->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1102]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1102"
-xref: delta_mono_mass "39.010899"
-xref: delta_avge_mass "39.036"
-xref: delta_composition "H C(2) N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:00:53"
-xref: date_time_modified "2011-06-21 14:00:53"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1103
-name: Gly->Phe
-def: "Gly->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1103]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1103"
-xref: delta_mono_mass "90.04695"
-xref: delta_avge_mass "90.1225"
-xref: delta_composition "H(6) C(7)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:03:41"
-xref: date_time_modified "2011-06-21 14:03:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1104
-name: Gly->His
-def: "Gly->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1104]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1104"
-xref: delta_mono_mass "80.037448"
-xref: delta_avge_mass "80.088"
-xref: delta_composition "H(4) C(4) N(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:04:05"
-xref: date_time_modified "2011-06-21 14:04:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1105
-name: Gly->Xle
-def: "Gly->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1105]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1105"
-xref: delta_mono_mass "56.0626"
-xref: delta_avge_mass "56.1063"
-xref: delta_composition "H(8) C(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:04:27"
-xref: date_time_modified "2011-06-21 15:15:58"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1106
-name: Gly->Lys
-def: "Gly->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1106]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1106"
-xref: delta_mono_mass "71.073499"
-xref: delta_avge_mass "71.121"
-xref: delta_composition "H(9) C(4) N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:04:51"
-xref: date_time_modified "2011-06-21 14:04:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1107
-name: Gly->Met
-def: "Gly->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1107]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1107"
-xref: delta_mono_mass "74.019021"
-xref: delta_avge_mass "74.1447"
-xref: delta_composition "H(6) C(3) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:05:16"
-xref: date_time_modified "2011-06-21 14:05:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1108
-name: Gly->Asn
-def: "Gly->Asn substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1108]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1108"
-xref: delta_mono_mass "57.021464"
-xref: delta_avge_mass "57.0513"
-xref: delta_composition "H(3) C(2) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:05:35"
-xref: date_time_modified "2011-06-21 14:05:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1109
-name: Gly->Pro
-def: "Gly->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1109]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1109"
-xref: delta_mono_mass "40.0313"
-xref: delta_avge_mass "40.0639"
-xref: delta_composition "H(4) C(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:05:55"
-xref: date_time_modified "2011-06-21 14:05:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1110
-name: Gly->Gln
-def: "Gly->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1110]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1110"
-xref: delta_mono_mass "71.037114"
-xref: delta_avge_mass "71.0779"
-xref: delta_composition "H(5) C(3) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:06:16"
-xref: date_time_modified "2011-06-21 14:06:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1111
-name: Gly->Thr
-def: "Gly->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1111]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1111"
-xref: delta_mono_mass "44.026215"
-xref: delta_avge_mass "44.0526"
-xref: delta_composition "H(4) C(2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:06:40"
-xref: date_time_modified "2011-06-21 14:06:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1112
-name: Gly->Tyr
-def: "Gly->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1112]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1112"
-xref: delta_mono_mass "106.041865"
-xref: delta_avge_mass "106.1219"
-xref: delta_composition "H(6) C(7) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:07:05"
-xref: date_time_modified "2011-06-21 14:07:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1113
-name: His->Ala
-def: "His->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1113]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1113"
-xref: delta_mono_mass "-66.021798"
-xref: delta_avge_mass "-66.0614"
-xref: delta_composition "H(-2) C(-3) N(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:51:31"
-xref: date_time_modified "2011-06-21 14:51:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1114
-name: His->Cys
-def: "His->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1114]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1114"
-xref: delta_mono_mass "-34.049727"
-xref: delta_avge_mass "-33.9964"
-xref: delta_composition "H(-2) C(-3) N(-2) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:51:56"
-xref: date_time_modified "2011-06-21 14:51:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1115
-name: His->Glu
-def: "His->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1115]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1115"
-xref: delta_mono_mass "-8.016319"
-xref: delta_avge_mass "-8.0253"
-xref: delta_composition "C(-1) N(-2) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:52:16"
-xref: date_time_modified "2011-06-21 14:52:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1116
-name: His->Phe
-def: "His->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1116]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1116"
-xref: delta_mono_mass "10.009502"
-xref: delta_avge_mass "10.0346"
-xref: delta_composition "H(2) C(3) N(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:52:50"
-xref: date_time_modified "2011-06-21 14:52:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1117
-name: His->Gly
-def: "His->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1117]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1117"
-xref: delta_mono_mass "-80.037448"
-xref: delta_avge_mass "-80.088"
-xref: delta_composition "H(-4) C(-4) N(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:53:45"
-xref: date_time_modified "2011-06-21 14:53:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1119
-name: His->Lys
-def: "His->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1119]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1119"
-xref: delta_mono_mass "-8.963949"
-xref: delta_avge_mass "-8.967"
-xref: delta_composition "H(5) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:59:08"
-xref: date_time_modified "2011-06-21 14:59:08"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1120
-name: His->Met
-def: "His->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1120]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1120"
-xref: delta_mono_mass "-6.018427"
-xref: delta_avge_mass "-5.9432"
-xref: delta_composition "H(2) C(-1) N(-2) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:59:30"
-xref: date_time_modified "2011-06-21 14:59:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1121
-name: His->Ser
-def: "His->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1121]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1121"
-xref: delta_mono_mass "-50.026883"
-xref: delta_avge_mass "-50.062"
-xref: delta_composition "H(-2) C(-3) N(-2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 14:59:50"
-xref: date_time_modified "2011-06-21 14:59:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1122
-name: His->Thr
-def: "His->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1122]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1122"
-xref: delta_mono_mass "-36.011233"
-xref: delta_avge_mass "-36.0354"
-xref: delta_composition "C(-2) N(-2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 15:00:20"
-xref: date_time_modified "2011-06-21 15:00:20"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1123
-name: His->Val
-def: "His->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1123]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1123"
-xref: delta_mono_mass "-37.990498"
-xref: delta_avge_mass "-38.0082"
-xref: delta_composition "H(2) C(-1) N(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 15:00:41"
-xref: date_time_modified "2011-06-21 15:00:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1124
-name: His->Trp
-def: "His->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1124]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1124"
-xref: delta_mono_mass "49.020401"
-xref: delta_avge_mass "49.0706"
-xref: delta_composition "H(3) C(5) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 15:01:02"
-xref: date_time_modified "2011-06-21 15:01:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1125
-name: Xle->Ala
-def: "Leu/Ile->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1125]
-xref: record_id "1125"
-xref: delta_mono_mass "-42.04695"
-xref: delta_avge_mass "-42.0797"
-xref: delta_composition "H(-6) C(-3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 15:33:19"
-xref: date_time_modified "2011-06-21 15:33:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "I"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1126
-name: Xle->Cys
-def: "Leu/Ile->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1126]
-xref: record_id "1126"
-xref: delta_mono_mass "-10.07488"
-xref: delta_avge_mass "-10.0147"
-xref: delta_composition "H(-6) C(-3) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 15:33:43"
-xref: date_time_modified "2011-06-21 15:33:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "I"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1127
-name: Xle->Asp
-def: "Leu/Ile->Asp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1127]
-xref: record_id "1127"
-xref: delta_mono_mass "1.942879"
-xref: delta_avge_mass "1.9298"
-xref: delta_composition "H(-6) C(-2) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 15:34:14"
-xref: date_time_modified "2011-06-21 15:34:14"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "I"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1128
-name: Xle->Glu
-def: "Leu/Ile->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1128]
-xref: record_id "1128"
-xref: delta_mono_mass "15.958529"
-xref: delta_avge_mass "15.9563"
-xref: delta_composition "H(-4) C(-1) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 15:34:40"
-xref: date_time_modified "2011-06-21 15:34:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "I"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1129
-name: Xle->Gly
-def: "Leu/Ile->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1129]
-xref: record_id "1129"
-xref: delta_mono_mass "-56.0626"
-xref: delta_avge_mass "-56.1063"
-xref: delta_composition "H(-8) C(-4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 15:35:12"
-xref: date_time_modified "2011-06-21 15:35:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "I"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1130
-name: Xle->Tyr
-def: "Leu/Ile->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1130]
-xref: record_id "1130"
-xref: delta_mono_mass "49.979265"
-xref: delta_avge_mass "50.0156"
-xref: delta_composition "H(-2) C(3) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 15:35:36"
-xref: date_time_modified "2011-06-21 15:35:36"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "I"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1131
-name: Lys->Ala
-def: "Lys->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1131]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1131"
-xref: delta_mono_mass "-57.057849"
-xref: delta_avge_mass "-57.0944"
-xref: delta_composition "H(-7) C(-3) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 15:37:25"
-xref: date_time_modified "2011-06-21 15:37:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1132
-name: Lys->Cys
-def: "Lys->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1132]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1132"
-xref: delta_mono_mass "-25.085779"
-xref: delta_avge_mass "-25.0294"
-xref: delta_composition "H(-7) C(-3) N(-1) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:01:01"
-xref: date_time_modified "2011-06-21 16:01:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1133
-name: Lys->Asp
-def: "Lys->Asp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1133]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1133"
-xref: delta_mono_mass "-13.06802"
-xref: delta_avge_mass "-13.0849"
-xref: delta_composition "H(-7) C(-2) N(-1) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:01:33"
-xref: date_time_modified "2011-06-21 16:01:33"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1134
-name: Lys->Phe
-def: "Lys->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1134]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1134"
-xref: delta_mono_mass "18.973451"
-xref: delta_avge_mass "19.0016"
-xref: delta_composition "H(-3) C(3) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:01:56"
-xref: date_time_modified "2011-06-21 16:01:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1135
-name: Lys->Gly
-def: "Lys->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1135]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1135"
-xref: delta_mono_mass "-71.073499"
-xref: delta_avge_mass "-71.121"
-xref: delta_composition "H(-9) C(-4) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:02:20"
-xref: date_time_modified "2011-06-21 16:02:20"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1136
-name: Lys->His
-def: "Lys->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1136]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1136"
-xref: delta_mono_mass "8.963949"
-xref: delta_avge_mass "8.967"
-xref: delta_composition "H(-5) N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:02:42"
-xref: date_time_modified "2011-06-21 16:02:42"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1137
-name: Lys->Pro
-def: "Lys->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1137]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1137"
-xref: delta_mono_mass "-31.042199"
-xref: delta_avge_mass "-31.0571"
-xref: delta_composition "H(-5) C(-1) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:03:06"
-xref: date_time_modified "2011-06-21 16:03:06"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1138
-name: Lys->Ser
-def: "Lys->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1138]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1138"
-xref: delta_mono_mass "-41.062935"
-xref: delta_avge_mass "-41.095"
-xref: delta_composition "H(-7) C(-3) N(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:03:27"
-xref: date_time_modified "2011-06-21 16:03:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1139
-name: Lys->Val
-def: "Lys->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1139]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1139"
-xref: delta_mono_mass "-29.026549"
-xref: delta_avge_mass "-29.0412"
-xref: delta_composition "H(-3) C(-1) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:03:49"
-xref: date_time_modified "2011-06-21 16:03:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1140
-name: Lys->Trp
-def: "Lys->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1140]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1140"
-xref: delta_mono_mass "57.98435"
-xref: delta_avge_mass "58.0376"
-xref: delta_composition "H(-2) C(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:04:11"
-xref: date_time_modified "2011-06-21 16:04:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1141
-name: Lys->Tyr
-def: "Lys->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1141]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1141"
-xref: delta_mono_mass "34.968366"
-xref: delta_avge_mass "35.001"
-xref: delta_composition "H(-3) C(3) N(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:04:35"
-xref: date_time_modified "2011-06-21 16:04:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1142
-name: Met->Ala
-def: "Met->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1142]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1142"
-xref: delta_mono_mass "-60.003371"
-xref: delta_avge_mass "-60.1182"
-xref: delta_composition "H(-4) C(-2) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:28:27"
-xref: date_time_modified "2011-06-21 16:28:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1143
-name: Met->Cys
-def: "Met->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1143]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1143"
-xref: delta_mono_mass "-28.0313"
-xref: delta_avge_mass "-28.0532"
-xref: delta_composition "H(-4) C(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:28:53"
-xref: date_time_modified "2011-06-21 16:28:53"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1144
-name: Met->Asp
-def: "Met->Asp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1144]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1144"
-xref: delta_mono_mass "-16.013542"
-xref: delta_avge_mass "-16.1087"
-xref: delta_composition "H(-4) C(-1) O(2) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:29:13"
-xref: date_time_modified "2011-06-21 16:29:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1145
-name: Met->Glu
-def: "Met->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1145]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1145"
-xref: delta_mono_mass "-1.997892"
-xref: delta_avge_mass "-2.0821"
-xref: delta_composition "H(-2) O(2) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:29:35"
-xref: date_time_modified "2011-06-21 16:29:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1146
-name: Met->Phe
-def: "Met->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1146]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1146"
-xref: delta_mono_mass "16.027929"
-xref: delta_avge_mass "15.9778"
-xref: delta_composition "C(4) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:30:07"
-xref: date_time_modified "2011-06-21 16:30:07"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1147
-name: Met->Gly
-def: "Met->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1147]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1147"
-xref: delta_mono_mass "-74.019021"
-xref: delta_avge_mass "-74.1447"
-xref: delta_composition "H(-6) C(-3) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:30:29"
-xref: date_time_modified "2011-06-21 16:30:29"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1148
-name: Met->His
-def: "Met->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1148]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1148"
-xref: delta_mono_mass "6.018427"
-xref: delta_avge_mass "5.9432"
-xref: delta_composition "H(-2) C N(2) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:30:50"
-xref: date_time_modified "2011-06-21 16:30:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1149
-name: Met->Asn
-def: "Met->Asn substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1149]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1149"
-xref: delta_mono_mass "-16.997557"
-xref: delta_avge_mass "-17.0934"
-xref: delta_composition "H(-3) C(-1) N O S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:31:14"
-xref: date_time_modified "2011-06-21 16:31:14"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1150
-name: Met->Pro
-def: "Met->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1150]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1150"
-xref: delta_mono_mass "-33.987721"
-xref: delta_avge_mass "-34.0809"
-xref: delta_composition "H(-2) S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:31:34"
-xref: date_time_modified "2011-06-21 16:31:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1151
-name: Met->Gln
-def: "Met->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1151]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1151"
-xref: delta_mono_mass "-2.981907"
-xref: delta_avge_mass "-3.0668"
-xref: delta_composition "H(-1) N O S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:31:55"
-xref: date_time_modified "2011-06-21 16:31:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1152
-name: Met->Ser
-def: "Met->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1152]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1152"
-xref: delta_mono_mass "-44.008456"
-xref: delta_avge_mass "-44.1188"
-xref: delta_composition "H(-4) C(-2) O S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:32:16"
-xref: date_time_modified "2011-06-21 16:32:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1153
-name: Met->Trp
-def: "Met->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1153]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1153"
-xref: delta_mono_mass "55.038828"
-xref: delta_avge_mass "55.0138"
-xref: delta_composition "H C(6) N S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:32:38"
-xref: date_time_modified "2011-06-21 16:32:38"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1154
-name: Met->Tyr
-def: "Met->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1154]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1154"
-xref: delta_mono_mass "32.022844"
-xref: delta_avge_mass "31.9772"
-xref: delta_composition "C(4) O S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:33:00"
-xref: date_time_modified "2011-06-21 16:33:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1155
-name: Asn->Ala
-def: "Asn->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1155]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1155"
-xref: delta_mono_mass "-43.005814"
-xref: delta_avge_mass "-43.0247"
-xref: delta_composition "H(-1) C(-1) N(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:36:38"
-xref: date_time_modified "2011-06-21 16:36:38"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1156
-name: Asn->Cys
-def: "Asn->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1156]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1156"
-xref: delta_mono_mass "-11.033743"
-xref: delta_avge_mass "-10.9597"
-xref: delta_composition "H(-1) C(-1) N(-1) O(-1) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:37:03"
-xref: date_time_modified "2011-06-21 16:37:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1157
-name: Asn->Glu
-def: "Asn->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1157]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1157"
-xref: delta_mono_mass "14.999666"
-xref: delta_avge_mass "15.0113"
-xref: delta_composition "H C N(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:37:26"
-xref: date_time_modified "2011-06-21 16:37:26"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1158
-name: Asn->Phe
-def: "Asn->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1158]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1158"
-xref: delta_mono_mass "33.025486"
-xref: delta_avge_mass "33.0712"
-xref: delta_composition "H(3) C(5) N(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:37:48"
-xref: date_time_modified "2011-06-21 16:37:48"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1159
-name: Asn->Gly
-def: "Asn->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1159]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1159"
-xref: delta_mono_mass "-57.021464"
-xref: delta_avge_mass "-57.0513"
-xref: delta_composition "H(-3) C(-2) N(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:38:11"
-xref: date_time_modified "2011-06-21 16:38:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1160
-name: Asn->Met
-def: "Asn->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1160]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1160"
-xref: delta_mono_mass "16.997557"
-xref: delta_avge_mass "17.0934"
-xref: delta_composition "H(3) C N(-1) O(-1) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:38:32"
-xref: date_time_modified "2011-06-21 16:38:32"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1161
-name: Asn->Pro
-def: "Asn->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1161]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1161"
-xref: delta_mono_mass "-16.990164"
-xref: delta_avge_mass "-16.9875"
-xref: delta_composition "H C N(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:38:54"
-xref: date_time_modified "2011-06-21 16:38:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1162
-name: Asn->Gln
-def: "Asn->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1162]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1162"
-xref: delta_mono_mass "14.01565"
-xref: delta_avge_mass "14.0266"
-xref: delta_composition "H(2) C"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:39:15"
-xref: date_time_modified "2011-06-21 16:39:15"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1163
-name: Asn->Arg
-def: "Asn->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1163]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1163"
-xref: delta_mono_mass "42.058184"
-xref: delta_avge_mass "42.083"
-xref: delta_composition "H(6) C(2) N(2) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:39:37"
-xref: date_time_modified "2011-06-21 16:39:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1164
-name: Asn->Val
-def: "Asn->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1164]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1164"
-xref: delta_mono_mass "-14.974514"
-xref: delta_avge_mass "-14.9716"
-xref: delta_composition "H(3) C N(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:39:59"
-xref: date_time_modified "2011-06-21 16:39:59"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1165
-name: Asn->Trp
-def: "Asn->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1165]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1165"
-xref: delta_mono_mass "72.036386"
-xref: delta_avge_mass "72.1073"
-xref: delta_composition "H(4) C(7) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:40:21"
-xref: date_time_modified "2011-06-21 16:40:21"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1166
-name: Pro->Cys
-def: "Pro->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1166]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1166"
-xref: delta_mono_mass "5.956421"
-xref: delta_avge_mass "6.0277"
-xref: delta_composition "H(-2) C(-2) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 16:59:55"
-xref: date_time_modified "2011-06-21 16:59:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1167
-name: Pro->Asp
-def: "Pro->Asp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1167]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1167"
-xref: delta_mono_mass "17.974179"
-xref: delta_avge_mass "17.9722"
-xref: delta_composition "H(-2) C(-1) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:00:24"
-xref: date_time_modified "2011-06-21 17:00:24"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1168
-name: Pro->Glu
-def: "Pro->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1168]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1168"
-xref: delta_mono_mass "31.989829"
-xref: delta_avge_mass "31.9988"
-xref: delta_composition "O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:26:36"
-xref: date_time_modified "2011-06-21 17:26:36"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1169
-name: Pro->Phe
-def: "Pro->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1169]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1169"
-xref: delta_mono_mass "50.01565"
-xref: delta_avge_mass "50.0587"
-xref: delta_composition "H(2) C(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:26:56"
-xref: date_time_modified "2011-06-21 17:26:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1170
-name: Pro->Gly
-def: "Pro->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1170]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1170"
-xref: delta_mono_mass "-40.0313"
-xref: delta_avge_mass "-40.0639"
-xref: delta_composition "H(-4) C(-3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:27:17"
-xref: date_time_modified "2011-06-21 17:27:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1171
-name: Pro->Lys
-def: "Pro->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1171]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1171"
-xref: delta_mono_mass "31.042199"
-xref: delta_avge_mass "31.0571"
-xref: delta_composition "H(5) C N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:27:38"
-xref: date_time_modified "2011-06-21 17:27:38"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1172
-name: Pro->Met
-def: "Pro->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1172]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1172"
-xref: delta_mono_mass "33.987721"
-xref: delta_avge_mass "34.0809"
-xref: delta_composition "H(2) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:27:57"
-xref: date_time_modified "2011-06-21 17:27:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1173
-name: Pro->Asn
-def: "Pro->Asn substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1173]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1173"
-xref: delta_mono_mass "16.990164"
-xref: delta_avge_mass "16.9875"
-xref: delta_composition "H(-1) C(-1) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:28:18"
-xref: date_time_modified "2011-06-21 17:28:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1174
-name: Pro->Val
-def: "Pro->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1174]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1174"
-xref: delta_mono_mass "2.01565"
-xref: delta_avge_mass "2.0159"
-xref: delta_composition "H(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:28:41"
-xref: date_time_modified "2011-06-21 17:28:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1175
-name: Pro->Trp
-def: "Pro->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1175]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1175"
-xref: delta_mono_mass "89.026549"
-xref: delta_avge_mass "89.0947"
-xref: delta_composition "H(3) C(6) N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:29:04"
-xref: date_time_modified "2011-06-21 17:29:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1176
-name: Pro->Tyr
-def: "Pro->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1176]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1176"
-xref: delta_mono_mass "66.010565"
-xref: delta_avge_mass "66.0581"
-xref: delta_composition "H(2) C(4) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:29:24"
-xref: date_time_modified "2011-06-21 17:29:24"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1177
-name: Gln->Ala
-def: "Gln->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1177]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1177"
-xref: delta_mono_mass "-57.021464"
-xref: delta_avge_mass "-57.0513"
-xref: delta_composition "H(-3) C(-2) N(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:39:52"
-xref: date_time_modified "2011-06-21 17:39:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1178
-name: Gln->Cys
-def: "Gln->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1178]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1178"
-xref: delta_mono_mass "-25.049393"
-xref: delta_avge_mass "-24.9863"
-xref: delta_composition "H(-3) C(-2) N(-1) O(-1) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:40:20"
-xref: date_time_modified "2011-06-21 17:40:20"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1179
-name: Gln->Asp
-def: "Gln->Asp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1179]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1179"
-xref: delta_mono_mass "-13.031634"
-xref: delta_avge_mass "-13.0418"
-xref: delta_composition "H(-3) C(-1) N(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:40:42"
-xref: date_time_modified "2011-06-21 17:40:42"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1180
-name: Gln->Phe
-def: "Gln->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1180]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1180"
-xref: delta_mono_mass "19.009836"
-xref: delta_avge_mass "19.0446"
-xref: delta_composition "H C(4) N(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:41:04"
-xref: date_time_modified "2011-06-21 17:41:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1181
-name: Gln->Gly
-def: "Gln->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1181]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1181"
-xref: delta_mono_mass "-71.037114"
-xref: delta_avge_mass "-71.0779"
-xref: delta_composition "H(-5) C(-3) N(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:41:24"
-xref: date_time_modified "2011-06-21 17:41:24"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1182
-name: Gln->Met
-def: "Gln->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1182]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1182"
-xref: delta_mono_mass "2.981907"
-xref: delta_avge_mass "3.0668"
-xref: delta_composition "H N(-1) O(-1) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:41:53"
-xref: date_time_modified "2011-06-21 17:41:53"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1183
-name: Gln->Asn
-def: "Gln->Asn substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1183]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1183"
-xref: delta_mono_mass "-14.01565"
-xref: delta_avge_mass "-14.0266"
-xref: delta_composition "H(-2) C(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:42:17"
-xref: date_time_modified "2011-06-21 17:42:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1184
-name: Gln->Ser
-def: "Gln->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1184]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1184"
-xref: delta_mono_mass "-41.026549"
-xref: delta_avge_mass "-41.0519"
-xref: delta_composition "H(-3) C(-2) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:42:37"
-xref: date_time_modified "2011-06-21 17:42:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1185
-name: Gln->Thr
-def: "Gln->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1185]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1185"
-xref: delta_mono_mass "-27.010899"
-xref: delta_avge_mass "-27.0253"
-xref: delta_composition "H(-1) C(-1) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:42:58"
-xref: date_time_modified "2011-06-21 17:42:58"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1186
-name: Gln->Val
-def: "Gln->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1186]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1186"
-xref: delta_mono_mass "-28.990164"
-xref: delta_avge_mass "-28.9982"
-xref: delta_composition "H N(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:43:20"
-xref: date_time_modified "2011-06-21 17:43:20"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1187
-name: Gln->Trp
-def: "Gln->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1187]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1187"
-xref: delta_mono_mass "58.020735"
-xref: delta_avge_mass "58.0807"
-xref: delta_composition "H(2) C(6) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:43:42"
-xref: date_time_modified "2011-06-21 17:43:42"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1188
-name: Gln->Tyr
-def: "Gln->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1188]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1188"
-xref: delta_mono_mass "35.004751"
-xref: delta_avge_mass "35.044"
-xref: delta_composition "H C(4) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-21 17:44:02"
-xref: date_time_modified "2011-06-21 17:44:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1189
-name: Arg->Ala
-def: "Arg->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1189]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1189"
-xref: delta_mono_mass "-85.063997"
-xref: delta_avge_mass "-85.1078"
-xref: delta_composition "H(-7) C(-3) N(-3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 10:47:36"
-xref: date_time_modified "2011-06-23 10:47:36"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1190
-name: Arg->Asp
-def: "Arg->Asp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1190]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1190"
-xref: delta_mono_mass "-41.074168"
-xref: delta_avge_mass "-41.0983"
-xref: delta_composition "H(-7) C(-2) N(-3) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 10:48:03"
-xref: date_time_modified "2011-06-23 10:48:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1191
-name: Arg->Glu
-def: "Arg->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1191]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1191"
-xref: delta_mono_mass "-27.058518"
-xref: delta_avge_mass "-27.0717"
-xref: delta_composition "H(-5) C(-1) N(-3) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 10:48:51"
-xref: date_time_modified "2011-06-23 10:48:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1192
-name: Arg->Asn
-def: "Arg->Asn substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1192]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1192"
-xref: delta_mono_mass "-42.058184"
-xref: delta_avge_mass "-42.083"
-xref: delta_composition "H(-6) C(-2) N(-2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 10:49:09"
-xref: date_time_modified "2011-06-23 10:49:29"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1193
-name: Arg->Val
-def: "Arg->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1193]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1193"
-xref: delta_mono_mass "-57.032697"
-xref: delta_avge_mass "-57.0546"
-xref: delta_composition "H(-3) C(-1) N(-3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 10:49:53"
-xref: date_time_modified "2011-06-23 10:49:53"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1194
-name: Arg->Tyr
-def: "Arg->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1194]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1194"
-xref: delta_mono_mass "6.962218"
-xref: delta_avge_mass "6.9876"
-xref: delta_composition "H(-3) C(3) N(-3) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 10:50:15"
-xref: date_time_modified "2011-06-23 10:50:15"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1195
-name: Arg->Phe
-def: "Arg->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1195]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1195"
-xref: delta_mono_mass "-9.032697"
-xref: delta_avge_mass "-9.0118"
-xref: delta_composition "H(-3) C(3) N(-3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 10:55:03"
-xref: date_time_modified "2011-06-23 10:55:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1196
-name: Ser->Asp
-def: "Ser->Asp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1196]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1196"
-xref: delta_mono_mass "27.994915"
-xref: delta_avge_mass "28.0101"
-xref: delta_composition "C O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 10:57:45"
-xref: date_time_modified "2011-06-23 10:57:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1197
-name: Ser->Glu
-def: "Ser->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1197]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1197"
-xref: delta_mono_mass "42.010565"
-xref: delta_avge_mass "42.0367"
-xref: delta_composition "H(2) C(2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 10:58:11"
-xref: date_time_modified "2011-06-23 10:58:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1198
-name: Ser->His
-def: "Ser->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1198]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1198"
-xref: delta_mono_mass "50.026883"
-xref: delta_avge_mass "50.062"
-xref: delta_composition "H(2) C(3) N(2) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 10:58:34"
-xref: date_time_modified "2011-06-23 10:58:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1199
-name: Ser->Lys
-def: "Ser->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1199]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1199"
-xref: delta_mono_mass "41.062935"
-xref: delta_avge_mass "41.095"
-xref: delta_composition "H(7) C(3) N O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 10:58:58"
-xref: date_time_modified "2011-06-23 10:58:58"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1200
-name: Ser->Met
-def: "Ser->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1200]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1200"
-xref: delta_mono_mass "44.008456"
-xref: delta_avge_mass "44.1188"
-xref: delta_composition "H(4) C(2) O(-1) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 10:59:19"
-xref: date_time_modified "2011-06-23 10:59:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1201
-name: Ser->Gln
-def: "Ser->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1201]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1201"
-xref: delta_mono_mass "41.026549"
-xref: delta_avge_mass "41.0519"
-xref: delta_composition "H(3) C(2) N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 10:59:38"
-xref: date_time_modified "2011-06-23 10:59:38"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1202
-name: Ser->Val
-def: "Ser->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1202]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1202"
-xref: delta_mono_mass "12.036386"
-xref: delta_avge_mass "12.0538"
-xref: delta_composition "H(4) C(2) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 10:59:59"
-xref: date_time_modified "2011-06-23 10:59:59"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1203
-name: Thr->Cys
-def: "Thr->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1203]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1203"
-xref: delta_mono_mass "1.961506"
-xref: delta_avge_mass "2.039"
-xref: delta_composition "H(-2) C(-1) O(-1) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:00:56"
-xref: date_time_modified "2011-06-23 11:00:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1204
-name: Thr->Asp
-def: "Thr->Asp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1204]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1204"
-xref: delta_mono_mass "13.979265"
-xref: delta_avge_mass "13.9835"
-xref: delta_composition "H(-2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:01:35"
-xref: date_time_modified "2011-06-23 11:01:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1205
-name: Thr->Glu
-def: "Thr->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1205]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1205"
-xref: delta_mono_mass "27.994915"
-xref: delta_avge_mass "28.0101"
-xref: delta_composition "C O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:02:00"
-xref: date_time_modified "2011-06-23 11:02:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1206
-name: Thr->Phe
-def: "Thr->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1206]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1206"
-xref: delta_mono_mass "46.020735"
-xref: delta_avge_mass "46.07"
-xref: delta_composition "H(2) C(5) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:02:21"
-xref: date_time_modified "2011-06-23 11:02:21"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1207
-name: Thr->Gly
-def: "Thr->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1207]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1207"
-xref: delta_mono_mass "-44.026215"
-xref: delta_avge_mass "-44.0526"
-xref: delta_composition "H(-4) C(-2) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:02:41"
-xref: date_time_modified "2011-06-23 11:02:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1208
-name: Thr->His
-def: "Thr->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1208]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1208"
-xref: delta_mono_mass "36.011233"
-xref: delta_avge_mass "36.0354"
-xref: delta_composition "C(2) N(2) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:03:03"
-xref: date_time_modified "2011-06-23 11:03:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1209
-name: Thr->Gln
-def: "Thr->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1209]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1209"
-xref: delta_mono_mass "27.010899"
-xref: delta_avge_mass "27.0253"
-xref: delta_composition "H C N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:03:26"
-xref: date_time_modified "2011-06-23 11:03:26"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1210
-name: Thr->Val
-def: "Thr->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1210]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1210"
-xref: delta_mono_mass "-1.979265"
-xref: delta_avge_mass "-1.9728"
-xref: delta_composition "H(2) C O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:03:48"
-xref: date_time_modified "2011-06-23 11:03:48"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1211
-name: Thr->Trp
-def: "Thr->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1211]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1211"
-xref: delta_mono_mass "85.031634"
-xref: delta_avge_mass "85.106"
-xref: delta_composition "H(3) C(7) N O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:04:08"
-xref: date_time_modified "2011-06-23 11:04:08"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1212
-name: Thr->Tyr
-def: "Thr->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1212]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1212"
-xref: delta_mono_mass "62.01565"
-xref: delta_avge_mass "62.0694"
-xref: delta_composition "H(2) C(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:04:28"
-xref: date_time_modified "2011-06-23 11:04:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1213
-name: Val->Cys
-def: "Val->Cys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1213]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1213"
-xref: delta_mono_mass "3.940771"
-xref: delta_avge_mass "4.0118"
-xref: delta_composition "H(-4) C(-2) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:19:57"
-xref: date_time_modified "2011-06-23 11:19:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1214
-name: Val->His
-def: "Val->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1214]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1214"
-xref: delta_mono_mass "37.990498"
-xref: delta_avge_mass "38.0082"
-xref: delta_composition "H(-2) C N(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:20:23"
-xref: date_time_modified "2011-06-23 11:20:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1215
-name: Val->Lys
-def: "Val->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1215]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1215"
-xref: delta_mono_mass "29.026549"
-xref: delta_avge_mass "29.0412"
-xref: delta_composition "H(3) C N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:20:45"
-xref: date_time_modified "2011-06-23 11:20:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1216
-name: Val->Asn
-def: "Val->Asn substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1216]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1216"
-xref: delta_mono_mass "14.974514"
-xref: delta_avge_mass "14.9716"
-xref: delta_composition "H(-3) C(-1) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:21:04"
-xref: date_time_modified "2011-06-23 11:21:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1217
-name: Val->Pro
-def: "Val->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1217]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1217"
-xref: delta_mono_mass "-2.01565"
-xref: delta_avge_mass "-2.0159"
-xref: delta_composition "H(-2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:21:23"
-xref: date_time_modified "2011-06-23 11:21:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1218
-name: Val->Gln
-def: "Val->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1218]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1218"
-xref: delta_mono_mass "28.990164"
-xref: delta_avge_mass "28.9982"
-xref: delta_composition "H(-1) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:21:42"
-xref: date_time_modified "2011-06-23 11:21:42"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1219
-name: Val->Arg
-def: "Val->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1219]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1219"
-xref: delta_mono_mass "57.032697"
-xref: delta_avge_mass "57.0546"
-xref: delta_composition "H(3) C N(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:22:05"
-xref: date_time_modified "2011-06-23 11:22:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1220
-name: Val->Ser
-def: "Val->Ser substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1220]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1220"
-xref: delta_mono_mass "-12.036386"
-xref: delta_avge_mass "-12.0538"
-xref: delta_composition "H(-4) C(-2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:22:26"
-xref: date_time_modified "2011-06-23 11:22:26"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1221
-name: Val->Thr
-def: "Val->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1221]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1221"
-xref: delta_mono_mass "1.979265"
-xref: delta_avge_mass "1.9728"
-xref: delta_composition "H(-2) C(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:22:49"
-xref: date_time_modified "2011-06-23 11:22:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1222
-name: Val->Trp
-def: "Val->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1222]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1222"
-xref: delta_mono_mass "87.010899"
-xref: delta_avge_mass "87.0788"
-xref: delta_composition "H C(6) N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:23:11"
-xref: date_time_modified "2011-06-23 11:23:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1223
-name: Val->Tyr
-def: "Val->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1223]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1223"
-xref: delta_mono_mass "63.994915"
-xref: delta_avge_mass "64.0422"
-xref: delta_composition "C(4) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:23:33"
-xref: date_time_modified "2011-06-23 11:23:33"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "V"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1224
-name: Trp->Ala
-def: "Trp->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1224]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1224"
-xref: delta_mono_mass "-115.042199"
-xref: delta_avge_mass "-115.132"
-xref: delta_composition "H(-5) C(-8) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:39:07"
-xref: date_time_modified "2011-06-23 11:39:07"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1225
-name: Trp->Asp
-def: "Trp->Asp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1225]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1225"
-xref: delta_mono_mass "-71.05237"
-xref: delta_avge_mass "-71.1225"
-xref: delta_composition "H(-5) C(-7) N(-1) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:40:26"
-xref: date_time_modified "2011-06-23 11:40:26"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1226
-name: Trp->Glu
-def: "Trp->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1226]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1226"
-xref: delta_mono_mass "-57.03672"
-xref: delta_avge_mass "-57.0959"
-xref: delta_composition "H(-3) C(-6) N(-1) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:40:48"
-xref: date_time_modified "2011-06-23 11:40:48"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1227
-name: Trp->Phe
-def: "Trp->Phe substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1227]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1227"
-xref: delta_mono_mass "-39.010899"
-xref: delta_avge_mass "-39.036"
-xref: delta_composition "H(-1) C(-2) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:41:09"
-xref: date_time_modified "2011-06-23 11:41:09"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1228
-name: Trp->His
-def: "Trp->His substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1228]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1228"
-xref: delta_mono_mass "-49.020401"
-xref: delta_avge_mass "-49.0706"
-xref: delta_composition "H(-3) C(-5) N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:41:32"
-xref: date_time_modified "2011-06-23 11:41:32"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1229
-name: Trp->Lys
-def: "Trp->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1229]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1229"
-xref: delta_mono_mass "-57.98435"
-xref: delta_avge_mass "-58.0376"
-xref: delta_composition "H(2) C(-5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:41:52"
-xref: date_time_modified "2011-06-23 11:41:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1230
-name: Trp->Met
-def: "Trp->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1230]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1230"
-xref: delta_mono_mass "-55.038828"
-xref: delta_avge_mass "-55.0138"
-xref: delta_composition "H(-1) C(-6) N(-1) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:42:11"
-xref: date_time_modified "2011-06-23 11:42:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1231
-name: Trp->Asn
-def: "Trp->Asn substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1231]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1231"
-xref: delta_mono_mass "-72.036386"
-xref: delta_avge_mass "-72.1073"
-xref: delta_composition "H(-4) C(-7) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:42:32"
-xref: date_time_modified "2011-06-23 11:42:32"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1232
-name: Trp->Pro
-def: "Trp->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1232]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1232"
-xref: delta_mono_mass "-89.026549"
-xref: delta_avge_mass "-89.0947"
-xref: delta_composition "H(-3) C(-6) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:42:53"
-xref: date_time_modified "2011-06-23 11:42:53"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1233
-name: Trp->Gln
-def: "Trp->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1233]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1233"
-xref: delta_mono_mass "-58.020735"
-xref: delta_avge_mass "-58.0807"
-xref: delta_composition "H(-2) C(-6) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:43:14"
-xref: date_time_modified "2011-06-23 11:43:14"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1234
-name: Trp->Thr
-def: "Trp->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1234]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1234"
-xref: delta_mono_mass "-85.031634"
-xref: delta_avge_mass "-85.106"
-xref: delta_composition "H(-3) C(-7) N(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:43:34"
-xref: date_time_modified "2011-06-23 11:43:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1235
-name: Trp->Val
-def: "Trp->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1235]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1235"
-xref: delta_mono_mass "-87.010899"
-xref: delta_avge_mass "-87.0788"
-xref: delta_composition "H(-1) C(-6) N(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:43:54"
-xref: date_time_modified "2011-06-23 11:43:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1236
-name: Trp->Tyr
-def: "Trp->Tyr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1236]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1236"
-xref: delta_mono_mass "-23.015984"
-xref: delta_avge_mass "-23.0366"
-xref: delta_composition "H(-1) C(-2) N(-1) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:44:18"
-xref: date_time_modified "2011-06-23 11:44:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1237
-name: Tyr->Ala
-def: "Tyr->Ala substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1237]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1237"
-xref: delta_mono_mass "-92.026215"
-xref: delta_avge_mass "-92.0954"
-xref: delta_composition "H(-4) C(-6) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:46:23"
-xref: date_time_modified "2011-06-23 11:46:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1238
-name: Tyr->Glu
-def: "Tyr->Glu substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1238]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1238"
-xref: delta_mono_mass "-34.020735"
-xref: delta_avge_mass "-34.0593"
-xref: delta_composition "H(-2) C(-4) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:46:45"
-xref: date_time_modified "2011-06-23 11:46:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1239
-name: Tyr->Gly
-def: "Tyr->Gly substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1239]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1239"
-xref: delta_mono_mass "-106.041865"
-xref: delta_avge_mass "-106.1219"
-xref: delta_composition "H(-6) C(-7) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:47:05"
-xref: date_time_modified "2011-06-23 11:47:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1240
-name: Tyr->Lys
-def: "Tyr->Lys substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1240]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1240"
-xref: delta_mono_mass "-34.968366"
-xref: delta_avge_mass "-35.001"
-xref: delta_composition "H(3) C(-3) N O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:47:23"
-xref: date_time_modified "2011-06-23 11:47:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1241
-name: Tyr->Met
-def: "Tyr->Met substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1241]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1241"
-xref: delta_mono_mass "-32.022844"
-xref: delta_avge_mass "-31.9772"
-xref: delta_composition "C(-4) O(-1) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:47:43"
-xref: date_time_modified "2011-06-23 11:47:43"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1242
-name: Tyr->Pro
-def: "Tyr->Pro substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1242]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1242"
-xref: delta_mono_mass "-66.010565"
-xref: delta_avge_mass "-66.0581"
-xref: delta_composition "H(-2) C(-4) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:48:07"
-xref: date_time_modified "2011-06-23 11:48:07"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1243
-name: Tyr->Gln
-def: "Tyr->Gln substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1243]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1243"
-xref: delta_mono_mass "-35.004751"
-xref: delta_avge_mass "-35.044"
-xref: delta_composition "H(-1) C(-4) N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:48:28"
-xref: date_time_modified "2011-06-23 11:48:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1244
-name: Tyr->Arg
-def: "Tyr->Arg substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1244]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1244"
-xref: delta_mono_mass "-6.962218"
-xref: delta_avge_mass "-6.9876"
-xref: delta_composition "H(3) C(-3) N(3) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:48:49"
-xref: date_time_modified "2011-06-23 11:48:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1245
-name: Tyr->Thr
-def: "Tyr->Thr substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1245]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1245"
-xref: delta_mono_mass "-62.01565"
-xref: delta_avge_mass "-62.0694"
-xref: delta_composition "H(-2) C(-5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:49:10"
-xref: date_time_modified "2011-06-23 11:49:10"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1246
-name: Tyr->Val
-def: "Tyr->Val substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1246]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1246"
-xref: delta_mono_mass "-63.994915"
-xref: delta_avge_mass "-64.0422"
-xref: delta_composition "C(-4) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:49:30"
-xref: date_time_modified "2011-06-23 11:49:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1247
-name: Tyr->Trp
-def: "Tyr->Trp substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1247]
-synonym: "Misacylation of the tRNA or editing of the charged tRNA" RELATED []
-xref: record_id "1247"
-xref: delta_mono_mass "23.015984"
-xref: delta_avge_mass "23.0366"
-xref: delta_composition "H C(2) N O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:49:50"
-xref: date_time_modified "2011-06-23 11:49:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1248
-name: Tyr->Xle
-def: "Tyr->Leu/Ile substitution." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1248]
-xref: record_id "1248"
-xref: delta_mono_mass "-49.979265"
-xref: delta_avge_mass "-50.0156"
-xref: delta_composition "H(2) C(-3) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-23 11:53:26"
-xref: date_time_modified "2011-06-23 11:53:26"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "AA substitution"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1249
-name: AHA-SS
-def: "Azidohomoalanine coupled to reductively cleaved tag." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1249]
-xref: record_id "1249"
-xref: delta_mono_mass "195.075625"
-xref: delta_avge_mass "195.1787"
-xref: delta_composition "H(9) C(7) N(5) O(2)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-24 10:58:26"
-xref: date_time_modified "2011-06-27 17:38:32"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Multiple"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1250
-name: AHA-SS_CAM
-def: "Carbamidomethylated form of reductively cleaved tag coupled to azidohomoalanine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1250]
-xref: record_id "1250"
-xref: delta_mono_mass "252.097088"
-xref: delta_avge_mass "252.23"
-xref: delta_composition "H(12) C(9) N(6) O(3)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-24 11:00:11"
-xref: date_time_modified "2011-06-27 17:39:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Multiple"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1251
-name: Biotin:Thermo-33033
-def: "Sulfo-SBED Label Photoreactive Biotin Crosslinker." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1251]
-xref: record_id "1251"
-xref: delta_mono_mass "548.223945"
-xref: delta_avge_mass "548.7211"
-xref: delta_composition "H(36) C(25) N(6) O(4) S(2)"
-xref: username_of_poster "Magnojunqueira"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-24 16:58:05"
-xref: date_time_modified "2013-04-16 23:21:26"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "Sulfo-SBED Label Transfer ReagentrnReaction path that does not remove one Hidrogen atom from the target peptide"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1252
-name: Biotin:Thermo-33033-H
-def: "Sulfo-SBED Label Photoreactive Biotin Crosslinker minus Hydrogen." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1252]
-xref: record_id "1252"
-xref: delta_mono_mass "546.208295"
-xref: delta_avge_mass "546.7053"
-xref: delta_composition "H(34) C(25) N(6) O(4) S(2)"
-xref: username_of_poster "Magnojunqueira"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-24 17:01:13"
-xref: date_time_modified "2011-06-24 21:16:06"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "Sulfo-SBED Label Transfer Reagent. Reaction path that removes one Hydrogen atom from the target peptide"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1253
-name: 2-monomethylsuccinyl
-def: "S-(2-monomethylsuccinyl) cysteine." [URL:http\://www.chemblink.com/products/2756-87-8.htm, PMID:http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=5369209, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1253]
-xref: record_id "1253"
-xref: delta_mono_mass "130.026609"
-xref: delta_avge_mass "130.0987"
-xref: delta_composition "H(6) C(5) O(4)"
-xref: username_of_poster "JMcGouran"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-28 15:27:43"
-xref: date_time_modified "2011-07-12 14:25:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1254
-name: Saligenin
-def: "O-toluene." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1254]
-comment: Believed to be created in a secondary reaction after initial formation of an adduct between the organophosphate 2-(o-cresyl)-4H-1,3,2-benzodioxaphosphorane-2-one and Tyr or Ser in proteins.
-xref: record_id "1254"
-xref: delta_mono_mass "106.041865"
-xref: delta_avge_mass "106.1219"
-xref: delta_composition "H(6) C(7) O"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-30 19:24:11"
-xref: date_time_modified "2011-07-09 09:17:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1255
-name: Cresylphosphate
-def: "O-toluyl-phosphorylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1255]
-comment: Created by hydrolysis of the product of the reaction of 2-(o-cresyl)-4H-1,3,2-benzodioxaphosphorane-2-one with amino acids residues in proteins.
-xref: record_id "1255"
-xref: delta_mono_mass "170.013281"
-xref: delta_avge_mass "170.1024"
-xref: delta_composition "H(7) C(7) O(3) P"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-30 19:33:14"
-xref: date_time_modified "2011-07-09 09:20:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "R"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "S"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "T"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "Y"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1256
-name: CresylSaligeninPhosphate
-def: "Cresyl-Saligenin-phosphorylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1256]
-comment: Created by reaction of 2-(o-cresyl)-4H-1,3,2-benzodioxaphosphorane-2-one with amino acid residues in proteins.
-xref: record_id "1256"
-xref: delta_mono_mass "276.055146"
-xref: delta_avge_mass "276.2244"
-xref: delta_composition "H(13) C(14) O(4) P"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2011-06-30 19:38:15"
-xref: date_time_modified "2011-07-09 09:21:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "R"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "S"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "T"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "Y"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1257
-name: Ub-Br2
-def: "Ub Bromide probe addition." [URL:http\://www.enzolifesciences.com/fileadmin/reports/els_0a605e18ec.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1257]
-synonym: "Active site DUB cystine modification with Br Ub probe Trypsin Digestion reminant of Ub Br probe" RELATED []
-xref: record_id "1257"
-xref: delta_mono_mass "100.063663"
-xref: delta_avge_mass "100.1191"
-xref: delta_composition "H(8) C(4) N(2) O"
-xref: username_of_poster "JMcGouran"
-xref: group_of_poster ""
-xref: date_time_posted "2011-07-01 13:25:05"
-xref: date_time_modified "2011-07-11 11:30:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1258
-name: Ub-VME
-def: "Ubiquitin vinylmethylester." [URL:http\://www.lifesensors.com/pdf/Ub-VME_datasheet.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1258]
-synonym: "Active site DUB cystine modification with VME Ub probe Trypsin Digestion reminant of Ub VMEr probe" RELATED []
-xref: record_id "1258"
-xref: delta_mono_mass "172.084792"
-xref: delta_avge_mass "172.1818"
-xref: delta_composition "H(12) C(7) N(2) O(3)"
-xref: username_of_poster "JMcGouran"
-xref: group_of_poster ""
-xref: date_time_posted "2011-07-01 13:27:56"
-xref: date_time_modified "2021-07-06 12:32:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1261
-name: Ub-fluorescein
-def: "Ub Fluorescein probe addition." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1261]
-comment: Unpublished chemically synthesized protein modification tool.
-synonym: "Active site DUB cystine modification with Fluorescein Ub probe Trypsin Digestion reminant of Ub Fluorescein probe" RELATED []
-xref: record_id "1261"
-xref: delta_mono_mass "597.209772"
-xref: delta_avge_mass "597.598"
-xref: delta_composition "H(29) C(31) N(6) O(7)"
-xref: username_of_poster "JMcGouran"
-xref: group_of_poster ""
-xref: date_time_posted "2011-07-01 13:49:56"
-xref: date_time_modified "2011-07-12 14:28:20"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1262
-name: 2-dimethylsuccinyl
-def: "S-(2-dimethylsuccinyl) cysteine." [PMID:http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=637568&loc=ec_rcs, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1262]
-xref: record_id "1262"
-xref: delta_mono_mass "144.042259"
-xref: delta_avge_mass "144.1253"
-xref: delta_composition "H(8) C(6) O(4)"
-xref: username_of_poster "JMcGouran"
-xref: group_of_poster ""
-xref: date_time_posted "2011-07-06 10:55:02"
-xref: date_time_modified "2011-07-12 14:25:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1263
-name: Gly
-def: "Addition of Glycine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1263]
-comment: Occasionally used as chemical tag. In most cases, +57 is actually over-alkylation with iodoacetamide.
-xref: record_id "1263"
-xref: delta_mono_mass "57.021464"
-xref: delta_avge_mass "57.0513"
-xref: delta_composition "H(3) C(2) N O"
-xref: username_of_poster "kstampe2"
-xref: group_of_poster ""
-xref: date_time_posted "2011-07-07 16:37:10"
-xref: date_time_modified "2020-10-05 09:16:08"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1264
-name: pupylation
-def: "Addition of GGE." [PMID:21738222, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1264]
-xref: record_id "1264"
-xref: delta_mono_mass "243.085521"
-xref: delta_avge_mass "243.2166"
-xref: delta_composition "H(13) C(9) N(3) O(5)"
-xref: username_of_poster "hbromage"
-xref: group_of_poster ""
-xref: date_time_posted "2011-07-13 21:34:29"
-xref: date_time_modified "2011-07-24 12:24:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1266
-name: Label:13C(4)
-def: "13C4 Methionine label." [URL:http\://www.pil.sdu.dk/silac_intro.htm, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1266]
-synonym: "SILAC" RELATED []
-xref: record_id "1266"
-xref: delta_mono_mass "4.013419"
-xref: delta_avge_mass "3.9706"
-xref: delta_composition "C(-4) 13C(4)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2011-07-27 09:55:40"
-xref: date_time_modified "2011-12-07 10:49:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1267
-name: Label:13C(4)+Oxidation
-def: "Oxidised 13C4 labelled Methionine." [URL:http\://www.pil.sdu.dk/silac_intro.htm, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1267]
-synonym: "SILAC" RELATED []
-xref: record_id "1267"
-xref: delta_mono_mass "20.008334"
-xref: delta_avge_mass "19.97"
-xref: delta_composition "C(-4) 13C(4) O"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2011-07-27 10:10:30"
-xref: date_time_modified "2011-08-05 14:17:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1270
-name: HCysThiolactone
-def: "N-Homocysteine thiolactone." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1270]
-xref: record_id "1270"
-xref: delta_mono_mass "117.024835"
-xref: delta_avge_mass "117.1695"
-xref: delta_composition "H(7) C(4) N O S"
-xref: username_of_poster "alejandro"
-xref: group_of_poster ""
-xref: date_time_posted "2011-09-15 19:31:10"
-xref: date_time_modified "2014-12-01 10:35:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_1_misc_notes "N-Homocysteine thiolactone is an acylating agent and can react with the E amino group of lysine residues"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1271
-name: HCysteinyl
-def: "S-homocysteinylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1271]
-xref: record_id "1271"
-xref: delta_mono_mass "133.019749"
-xref: delta_avge_mass "133.1689"
-xref: delta_composition "H(7) C(4) N O(2) S"
-xref: username_of_poster "alejandro"
-xref: group_of_poster ""
-xref: date_time_posted "2011-09-15 19:36:44"
-xref: date_time_modified "2024-08-12 10:20:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_1_misc_notes "Homocysteine can take part in disulfide exchange reactions with S-S bonds in proteins, thus forming S-homocysteinylated proteins"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1276
-name: UgiJoullie
-def: "Side reaction of HisTag." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1276]
-comment: Side product of the three component Ugi-Joullie reaction. Pirrolidine is reacted with a isocianide modificated peptide (CNGGHHHHHH) to get a Pro-Gly-GGHHHHHH. The main product is the C-terminal modified protein. Unlikely Asp and Glu can react.
-xref: record_id "1276"
-xref: delta_mono_mass "1106.48935"
-xref: delta_avge_mass "1107.1274"
-xref: delta_composition "H(60) C(47) N(23) O(10)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2011-09-26 12:42:53"
-xref: date_time_modified "2011-09-30 12:38:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "E"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1277
-name: Dipyridyl
-def: "Cys modified with dipy ligand." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1277]
-comment: Cysteine residue reacts with a chlorinated dipyridyl ligand to get a monoalkylated Cys-L1. The only product is this single cys mutant modified on that position.
-xref: record_id "1277"
-xref: delta_mono_mass "225.090212"
-xref: delta_avge_mass "225.2459"
-xref: delta_composition "H(11) C(13) N(3) O"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2011-09-27 18:33:34"
-xref: date_time_modified "2012-01-20 14:46:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1278
-name: Furan
-def: "Chemical modification of the iodinated sites of thyroglobulin by Suzuki reaction." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1278]
-xref: record_id "1278"
-xref: delta_mono_mass "66.010565"
-xref: delta_avge_mass "66.0581"
-xref: delta_composition "H(2) C(4) O"
-xref: username_of_poster "chem0303"
-xref: group_of_poster ""
-xref: date_time_posted "2011-09-28 13:31:35"
-xref: date_time_modified "2011-09-30 12:39:48"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1279
-name: Difuran
-def: "Chemical modification of the diiodinated sites of thyroglobulin by Suzuki reaction." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1279]
-xref: record_id "1279"
-xref: delta_mono_mass "132.021129"
-xref: delta_avge_mass "132.1162"
-xref: delta_composition "H(4) C(8) O(2)"
-xref: username_of_poster "chem0303"
-xref: group_of_poster ""
-xref: date_time_posted "2011-09-28 13:34:45"
-xref: date_time_modified "2011-09-30 12:40:21"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1281
-name: BMP-piperidinol
-def: "1-methyl-3-benzoyl-4-hydroxy-4-phenylpiperidine." [PMID:http://www.ncbi.nlm.nih.gov/pubmed/11869872, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1281]
-synonym: "(4-hydroxy-1-methyl-4-phenylpiperidin-3-yl)(phenyl)methanone 3-benzoyl-1-methyl-4-phenyl-4-piperidinol" RELATED []
-xref: record_id "1281"
-xref: delta_mono_mass "263.131014"
-xref: delta_avge_mass "263.3337"
-xref: delta_composition "H(17) C(18) N O"
-xref: username_of_poster "Areej"
-xref: group_of_poster ""
-xref: date_time_posted "2011-10-12 12:22:26"
-xref: date_time_modified "2012-01-13 15:44:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1282
-name: UgiJoullieProGly
-def: "Side reaction of PG with Side chain of aspartic or glutamic acid." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1282]
-comment: Side product of the three component Ugi-Joullie reaction. Pirrolidine is reacted with a isocianide modificated glycine to get Protein-Pro-Gly. The main product is the C-terminal modified protein. Unlikely Asp and Glu can react.
-xref: record_id "1282"
-xref: delta_mono_mass "154.074228"
-xref: delta_avge_mass "154.1665"
-xref: delta_composition "H(10) C(7) N(2) O(2)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2011-10-14 18:11:28"
-xref: date_time_modified "2011-10-21 16:41:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "E"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1283
-name: UgiJoullieProGlyProGly
-def: "Side reaction of PGPG with Side chain of aspartic or glutamic acid." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1283]
-comment: Side product of the three component Ugi-Joullie reaction. Pirrolidine is reacted with a isocianide modificated glycine to get Protein-Pro-Gly-Pro-Gly. The main product is the C-terminal modified protein. Unlikely Asp and Glu can react.
-xref: record_id "1283"
-xref: delta_mono_mass "308.148455"
-xref: delta_avge_mass "308.333"
-xref: delta_composition "H(20) C(14) N(4) O(4)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2011-10-14 18:14:19"
-xref: date_time_modified "2011-10-21 16:40:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "E"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1286
-name: IMEHex(2)NeuAc(1)
-def: "Glycosylation with IME linked Hex(2) NeuAc." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1286]
-comment: Modification by Hex(2) NeuAc using IME coupling to get glycosylated proteins.
-synonym: "(2-Imino-2-methoxyethyl 1-thioglycoside)" RELATED []
-xref: record_id "1286"
-xref: delta_mono_mass "688.199683"
-xref: delta_avge_mass "688.6527"
-xref: delta_composition "H(3) C(2) N S Hex(2) NeuAc"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-11 12:06:36"
-xref: date_time_modified "2015-05-01 14:20:42"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other glycosylation"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1287
-name: Arg-loss
-def: "Loss of arginine due to transpeptidation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1287]
-xref: record_id "1287"
-xref: delta_mono_mass "-156.101111"
-xref: delta_avge_mass "-156.1857"
-xref: delta_composition "H(-12) C(-6) N(-4) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-21 10:12:18"
-xref: date_time_modified "2011-11-24 16:39:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Any C-term"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1288
-name: Arg
-def: "Addition of arginine due to transpeptidation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1288]
-xref: record_id "1288"
-xref: delta_mono_mass "156.101111"
-xref: delta_avge_mass "156.1857"
-xref: delta_composition "H(12) C(6) N(4) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-21 10:15:00"
-xref: date_time_modified "2011-11-21 10:17:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1289
-name: Butyryl
-def: "Butyryl." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1289]
-xref: record_id "1289"
-xref: delta_mono_mass "70.041865"
-xref: delta_avge_mass "70.0898"
-xref: delta_composition "H(6) C(4) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-21 12:06:20"
-xref: date_time_modified "2024-08-12 10:01:08"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1290
-name: Dicarbamidomethyl
-def: "Double Carbamidomethylation." [PMID:18511913, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1290]
-comment: Mentioned by Marshall Bern.
-xref: record_id "1290"
-xref: delta_mono_mass "114.042927"
-xref: delta_avge_mass "114.1026"
-xref: delta_composition "H(6) C(4) N(2) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-21 13:21:06"
-xref: date_time_modified "2013-05-16 10:59:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Artefact"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "R"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Artefact"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "N-term"
-xref: spec_5_position "Any N-term"
-xref: spec_5_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1291
-name: Dimethyl:2H(6)
-def: "Dimethyl-Medium." [PMID:15782174, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1291]
-xref: record_id "1291"
-xref: delta_mono_mass "34.068961"
-xref: delta_avge_mass "34.0901"
-xref: delta_composition "H(-2) 2H(6) C(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-21 13:27:00"
-xref: date_time_modified "2013-02-22 12:32:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "R"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1292
-name: GGQ
-def: "SUMOylation leaving GlyGlyGln." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1292]
-xref: record_id "1292"
-xref: delta_mono_mass "242.101505"
-xref: delta_avge_mass "242.2319"
-xref: delta_composition "H(14) C(9) N(4) O(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-21 13:37:45"
-xref: date_time_modified "2011-11-21 13:53:21"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_1_misc_notes "This peptide is generated from a trypsin/chymotrypsin dual digest."
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1293
-name: QTGG
-def: "SUMOylation leaving GlnThrGlyGly." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1293]
-xref: record_id "1293"
-xref: delta_mono_mass "343.149184"
-xref: delta_avge_mass "343.3357"
-xref: delta_composition "H(21) C(13) N(5) O(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-21 13:41:32"
-xref: date_time_modified "2011-11-25 13:05:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_1_misc_notes "This peptide is generated from a trypsin/chymotrypsin dual digest."
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1296
-name: Label:13C(3)
-def: "13C3 label for SILAC." [URL:http\://www.pil.sdu.dk/silac_intro.htm, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1296]
-xref: record_id "1296"
-xref: delta_mono_mass "3.010064"
-xref: delta_avge_mass "2.978"
-xref: delta_composition "C(-3) 13C(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-21 14:36:18"
-xref: date_time_modified "2011-11-21 14:37:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1297
-name: Label:13C(3)15N(1)
-def: "SILAC or AQUA label." [URL:http\://www.pil.sdu.dk/silac_intro.htm, URL:https\://www.thermofisher.com/order/catalog/product/A40010#/A40010, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1297]
-xref: record_id "1297"
-xref: delta_mono_mass "4.007099"
-xref: delta_avge_mass "3.9714"
-xref: delta_composition "C(-3) 13C(3) N(-1) 15N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-21 14:37:53"
-xref: date_time_modified "2020-01-09 09:44:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1298
-name: Label:13C(4)15N(1)
-def: "13C4 15N1 label for SILAC." [URL:http\://www.pil.sdu.dk/silac_intro.htm, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1298]
-xref: record_id "1298"
-xref: delta_mono_mass "5.010454"
-xref: delta_avge_mass "4.964"
-xref: delta_composition "C(-4) 13C(4) N(-1) 15N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-21 14:40:56"
-xref: date_time_modified "2011-11-21 14:40:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1299
-name: Label:2H(10)
-def: "2H(10) label." [URL:http\://www.pil.sdu.dk/silac_intro.htm, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1299]
-xref: record_id "1299"
-xref: delta_mono_mass "10.062767"
-xref: delta_avge_mass "10.0616"
-xref: delta_composition "H(-10) 2H(10)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-21 14:51:01"
-xref: date_time_modified "2011-11-21 14:51:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "L"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1300
-name: Label:2H(4)13C(1)
-def: "Label:2H(4)13C(1)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1300]
-comment: For SILAC experiments.
-xref: record_id "1300"
-xref: delta_mono_mass "5.028462"
-xref: delta_avge_mass "5.0173"
-xref: delta_composition "H(-4) 2H(4) C(-1) 13C"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-21 14:52:54"
-xref: date_time_modified "2011-11-21 14:52:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1301
-name: Lys
-def: "Addition of lysine due to transpeptidation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1301]
-xref: record_id "1301"
-xref: delta_mono_mass "128.094963"
-xref: delta_avge_mass "128.1723"
-xref: delta_composition "H(12) C(6) N(2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-21 14:56:07"
-xref: date_time_modified "2015-05-06 12:07:14"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1302
-name: mTRAQ:13C(6)15N(2)
-def: "MTRAQ heavy." [URL:http\://www3.appliedbiosystems.com/cms/groups/psm_support/documents/generaldocuments/cms_054141.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1302]
-synonym: "Applied Biosystems mTRAQ(TM) reagent" RELATED []
-xref: record_id "1302"
-xref: delta_mono_mass "148.109162"
-xref: delta_avge_mass "148.1257"
-xref: delta_composition "H(12) C 13C(6) 15N(2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-25 10:35:32"
-xref: date_time_modified "2011-11-25 10:35:32"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "0"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Low abundance"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "H"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "Very low abundance"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "S"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Isotopic label"
-xref: spec_5_misc_notes "Very low abundance"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "T"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Isotopic label"
-xref: spec_6_misc_notes "Very low abundance"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1303
-name: NeuAc
-def: "N-acetyl neuraminic acid." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1303]
-xref: record_id "1303"
-xref: delta_mono_mass "291.095417"
-xref: delta_avge_mass "291.2546"
-xref: delta_composition "NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-25 10:40:54"
-xref: date_time_modified "2015-05-01 15:11:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_292_mono_mass "291.095417"
-xref: spec_1_neutral_loss_292_avge_mass "291.2546"
-xref: spec_1_neutral_loss_292_flag "false"
-xref: spec_1_neutral_loss_292_composition "NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_292_mono_mass "291.095417"
-xref: spec_2_neutral_loss_292_avge_mass "291.2546"
-xref: spec_2_neutral_loss_292_flag "false"
-xref: spec_2_neutral_loss_292_composition "NeuAc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_292_mono_mass "291.095417"
-xref: spec_2_neutral_loss_292_avge_mass "291.2546"
-xref: spec_2_neutral_loss_292_flag "false"
-xref: spec_2_neutral_loss_292_composition "NeuAc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1304
-name: NeuGc
-def: "N-glycoyl neuraminic acid." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1304]
-xref: record_id "1304"
-xref: delta_mono_mass "307.090331"
-xref: delta_avge_mass "307.254"
-xref: delta_composition "NeuGc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-25 10:41:35"
-xref: date_time_modified "2015-05-01 15:13:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_308_mono_mass "307.090331"
-xref: spec_1_neutral_loss_308_avge_mass "307.254"
-xref: spec_1_neutral_loss_308_flag "false"
-xref: spec_1_neutral_loss_308_composition "NeuGc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_308_mono_mass "307.090331"
-xref: spec_2_neutral_loss_308_avge_mass "307.254"
-xref: spec_2_neutral_loss_308_flag "false"
-xref: spec_2_neutral_loss_308_composition "NeuGc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_308_mono_mass "307.090331"
-xref: spec_2_neutral_loss_308_avge_mass "307.254"
-xref: spec_2_neutral_loss_308_flag "false"
-xref: spec_2_neutral_loss_308_composition "NeuGc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1305
-name: Propyl
-def: "Propyl." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1305]
-xref: record_id "1305"
-xref: delta_mono_mass "42.04695"
-xref: delta_avge_mass "42.0797"
-xref: delta_composition "H(6) C(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-25 11:06:09"
-xref: date_time_modified "2014-10-17 11:31:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "D"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_misc_notes "propyl ester"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "E"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_4_misc_notes "propyl ester"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "C-term"
-xref: spec_5_position "Any C-term"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_5_misc_notes "propyl ester"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "C-term"
-xref: spec_6_position "Protein C-term"
-xref: spec_6_classification "Chemical derivative"
-xref: spec_6_misc_notes "propyl ester"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1306
-name: Propyl:2H(6)
-def: "Propyl:2H(6)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1306]
-xref: record_id "1306"
-xref: delta_mono_mass "48.084611"
-xref: delta_avge_mass "48.1167"
-xref: delta_composition "2H(6) C(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2011-11-25 11:06:56"
-xref: date_time_modified "2011-11-25 11:06:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1310
-name: Propiophenone
-def: "Propiophenone." [PMID:http://www.ncbi.nlm.nih.gov/pubmed/11869872, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1310]
-xref: record_id "1310"
-xref: delta_mono_mass "132.057515"
-xref: delta_avge_mass "132.1592"
-xref: delta_composition "H(8) C(9) O"
-xref: username_of_poster "Areej"
-xref: group_of_poster ""
-xref: date_time_posted "2011-12-07 23:43:34"
-xref: date_time_modified "2011-12-09 13:50:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "R"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "S"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "T"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "W"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "C"
-xref: spec_7_position "Anywhere"
-xref: spec_7_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1312
-name: Delta:H(6)C(3)O(1)
-def: "Reduced acrolein addition +58." [PMID:21778411, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1312]
-xref: record_id "1312"
-xref: delta_mono_mass "58.041865"
-xref: delta_avge_mass "58.0791"
-xref: delta_composition "H(6) C(3) O"
-xref: username_of_poster "yiyingzhu"
-xref: group_of_poster ""
-xref: date_time_posted "2011-12-15 19:38:31"
-xref: date_time_modified "2011-12-16 15:11:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "N-term"
-xref: spec_4_position "Protein N-term"
-xref: spec_4_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1313
-name: Delta:H(8)C(6)O(1)
-def: "Reduced acrolein addition +96." [PMID:21778411, PMID:9632657, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1313]
-xref: record_id "1313"
-xref: delta_mono_mass "96.057515"
-xref: delta_avge_mass "96.1271"
-xref: delta_composition "H(8) C(6) O"
-xref: username_of_poster "yiyingzhu"
-xref: group_of_poster ""
-xref: date_time_posted "2011-12-15 19:48:15"
-xref: date_time_modified "2015-10-12 16:16:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1314
-name: biotinAcrolein298
-def: "Biotin hydrazide labeled acrolein addition +298." [PMID:21704744, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1314]
-xref: record_id "1314"
-xref: delta_mono_mass "298.146347"
-xref: delta_avge_mass "298.4044"
-xref: delta_composition "H(22) C(13) N(4) O(2) S"
-xref: username_of_poster "yiyingzhu"
-xref: group_of_poster ""
-xref: date_time_posted "2011-12-15 19:54:52"
-xref: date_time_modified "2011-12-16 15:19:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "N-term"
-xref: spec_4_position "Protein N-term"
-xref: spec_4_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1315
-name: MM-diphenylpentanone
-def: "3-methyl-5-(methylamino)-1,3-diphenylpentan-1-one." [PMID:http://www.ncbi.nlm.nih.gov/pubmed/11869872, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1315]
-xref: record_id "1315"
-xref: delta_mono_mass "265.146664"
-xref: delta_avge_mass "265.3496"
-xref: delta_composition "H(19) C(18) N O"
-xref: username_of_poster "Areej"
-xref: group_of_poster ""
-xref: date_time_posted "2011-12-21 21:29:00"
-xref: date_time_modified "2011-12-21 21:29:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1317
-name: EHD-diphenylpentanone
-def: "2-ethyl-3-hydroxy-1,3-diphenylpentan-1-one." [PMID:http://www.ncbi.nlm.nih.gov/pubmed/11869872, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1317]
-synonym: "3-benzoyl-1-methyl-4-phenyl-4-piperidinol demethyl damino" RELATED []
-xref: record_id "1317"
-xref: delta_mono_mass "266.13068"
-xref: delta_avge_mass "266.3343"
-xref: delta_composition "H(18) C(18) O(2)"
-xref: username_of_poster "Areej"
-xref: group_of_poster ""
-xref: date_time_posted "2012-01-08 15:22:49"
-xref: date_time_modified "2012-01-13 15:41:26"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "M"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1320
-name: Biotin:Thermo-21901+2H2O
-def: "Maleimide-Biotin + 2Water." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1320]
-synonym: "Maleimide-PEG2-Biotin + 2Water" RELATED []
-xref: record_id "1320"
-xref: delta_mono_mass "561.246849"
-xref: delta_avge_mass "561.6489"
-xref: delta_composition "H(39) C(23) N(5) O(9) S"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2012-01-23 14:20:11"
-xref: date_time_modified "2012-01-27 12:51:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1321
-name: DiLeu4plex115
-def: "Accurate mass for DiLeu 115 isobaric tag." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1321]
-comment: Different channels have the same nominal mass but slightly different exact masses.
-xref: record_id "1321"
-xref: delta_mono_mass "145.12"
-xref: delta_avge_mass "145.1966"
-xref: delta_composition "H(15) C(7) 13C 15N 18O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2012-02-15 12:05:08"
-xref: date_time_modified "2024-08-12 10:00:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Low abundance"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1322
-name: DiLeu4plex
-def: "Accurate mass for DiLeu 116 isobaric tag." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1322]
-comment: Different channels have the same nominal mass but slightly different exact masses.
-synonym: "Representative, nominal mass for all four tags" RELATED []
-xref: record_id "1322"
-xref: delta_mono_mass "145.132163"
-xref: delta_avge_mass "145.2229"
-xref: delta_composition "H(13) 2H(2) C(8) N 18O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2012-02-15 12:05:48"
-xref: date_time_modified "2024-08-12 10:00:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Low abundance"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1323
-name: DiLeu4plex117
-def: "Accurate mass for DiLeu 117 isobaric tag." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1323]
-comment: Different channels have the same nominal mass but slightly different exact masses.
-xref: record_id "1323"
-xref: delta_mono_mass "145.128307"
-xref: delta_avge_mass "145.2092"
-xref: delta_composition "H(13) 2H(2) C(7) 13C 15N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2012-02-15 12:06:10"
-xref: date_time_modified "2024-08-12 10:00:14"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Low abundance"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1324
-name: DiLeu4plex118
-def: "Accurate mass for DiLeu 118 isobaric tag." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1324]
-comment: Different channels have the same nominal mass but slightly different exact masses.
-xref: record_id "1324"
-xref: delta_mono_mass "145.140471"
-xref: delta_avge_mass "145.2354"
-xref: delta_composition "H(11) 2H(4) C(8) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2012-02-15 12:06:30"
-xref: date_time_modified "2024-08-12 09:59:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Isotopic label"
-xref: spec_3_misc_notes "Low abundance"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1326
-name: NEMsulfur
-def: "N-ethylmaleimideSulfur." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1326]
-synonym: "NEMS" RELATED []
-xref: record_id "1326"
-xref: delta_mono_mass "157.019749"
-xref: delta_avge_mass "157.1903"
-xref: delta_composition "H(7) C(6) N O(2) S"
-xref: username_of_poster "Raghothama"
-xref: group_of_poster ""
-xref: date_time_posted "2012-02-29 17:06:24"
-xref: date_time_modified "2012-03-09 11:26:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1327
-name: SulfurDioxide
-def: "SulfurDioxide." [PMID:http://www.ncbi.nlm.nih.gov/pubmed/21740851, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1327]
-xref: record_id "1327"
-xref: delta_mono_mass "63.9619"
-xref: delta_avge_mass "64.0638"
-xref: delta_composition "O(2) S"
-xref: username_of_poster "Raghothama"
-xref: group_of_poster ""
-xref: date_time_posted "2012-02-29 17:24:24"
-xref: date_time_modified "2012-03-09 11:25:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1328
-name: NEMsulfurWater
-def: "N-ethylmaleimideSulfurWater." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1328]
-synonym: "NEMSwater" RELATED []
-xref: record_id "1328"
-xref: delta_mono_mass "175.030314"
-xref: delta_avge_mass "175.2056"
-xref: delta_composition "H(9) C(6) N O(3) S"
-xref: username_of_poster "Raghothama"
-xref: group_of_poster ""
-xref: date_time_posted "2012-02-29 17:25:30"
-xref: date_time_modified "2012-03-09 11:24:53"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1330
-name: bisANS-sulfonates
-def: "BisANS with loss of both sulfonates." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1330]
-xref: record_id "1330"
-xref: delta_mono_mass "434.178299"
-xref: delta_avge_mass "434.5305"
-xref: delta_composition "H(22) C(32) N(2)"
-xref: username_of_poster "app95d"
-xref: group_of_poster ""
-xref: date_time_posted "2012-05-22 21:55:58"
-xref: date_time_modified "2021-07-06 12:33:24"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1331
-name: DNCB_hapten
-def: "Chemical reaction with 2,4-dinitro-1-chloro benzene (DNCB)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1331]
-comment: Chemical reaction with 2,4-dinitro-1-chloro benzene (DNCB) by nucleophilic attack on electrophilic amino acid side chains.
-xref: record_id "1331"
-xref: delta_mono_mass "166.001457"
-xref: delta_avge_mass "166.0911"
-xref: delta_composition "H(2) C(6) N(2) O(4)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2012-05-24 13:55:30"
-xref: date_time_modified "2012-08-03 09:19:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "Y"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1340
-name: Biotin:Thermo-21911
-def: "Biotin-PEG11-maleimide." [URL:http\://www.piercenet.com/browse.cfm?fldID=E3862D31-9A5C-4F0A-9879-F600D33BD926, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1340]
-synonym: "Thermo #21911" RELATED []
-xref: record_id "1340"
-xref: delta_mono_mass "921.461652"
-xref: delta_avge_mass "922.0913"
-xref: delta_composition "H(71) C(41) N(5) O(16) S"
-xref: username_of_poster "Jolein_Gloerich"
-xref: group_of_poster ""
-xref: date_time_posted "2012-06-26 17:49:31"
-xref: date_time_modified "2012-07-14 19:02:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1341
-name: iodoTMT
-def: "Native iodoacetyl Tandem Mass Tag®." [URL:http\://www.lifetechnologies.com/order/catalog/product/90100, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1341]
-comment: This modification describes the native iodoTMT Reagent without isotopic label. Upon CID, this reagent releases a reporter ion of 126.127725(monoisotopic mass).
-synonym: "Tandem Mass Tag® and TMT® are registered Trademarks of Proteome Sciences plc. iodoTMTzero iodoTMT0" RELATED []
-xref: record_id "1341"
-xref: delta_mono_mass "324.216141"
-xref: delta_avge_mass "324.4185"
-xref: delta_composition "H(28) C(16) N(4) O(3)"
-xref: username_of_poster "rbomgard"
-xref: group_of_poster ""
-xref: date_time_posted "2012-07-06 17:37:43"
-xref: date_time_modified "2024-08-12 10:07:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "D"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "E"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "H"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "K"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1342
-name: iodoTMT6plex
-def: "Sixplex iodoacetyl Tandem Mass Tag®." [URL:http\://www.lifetechnologies.com/order/catalog/product/90102, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1342]
-comment: This modification describes the native iodoTMT Reagent without isotopic label. Upon CID, this reagent releases a reporter ions of 126.127725, 127.124760, 128.134433, 129.131468, 130.141141, and 131.138176 (monoisotopic mass).
-synonym: "Tandem Mass Tag® and TMT® are registered Trademarks of Proteome Sciences plc. iodoTMTsixplex iodoTMT6" RELATED []
-xref: record_id "1342"
-xref: delta_mono_mass "329.226595"
-xref: delta_avge_mass "329.3825"
-xref: delta_composition "H(28) C(12) 13C(4) N(3) 15N O(3)"
-xref: username_of_poster "rbomgard"
-xref: group_of_poster ""
-xref: date_time_posted "2012-07-06 17:43:59"
-xref: date_time_modified "2024-08-12 10:06:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "D"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "E"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "H"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "K"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1344
-name: Phosphogluconoylation
-def: "Phosphogluconoylation." [URL:http\://www.abrf.org/index.cfm/dm.details?DMID=275&AvgMass=258&Margin=0, PMID:18083862, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1344]
-xref: record_id "1344"
-xref: delta_mono_mass "258.014069"
-xref: delta_avge_mass "258.1199"
-xref: delta_composition "H(11) C(6) O(9) P"
-xref: username_of_poster "gwadams"
-xref: group_of_poster ""
-xref: date_time_posted "2012-07-13 14:40:15"
-xref: date_time_modified "2013-05-22 10:55:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1345
-name: PS_Hapten
-def: "Reaction with phenyl salicylate (PS)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1345]
-xref: record_id "1345"
-xref: delta_mono_mass "120.021129"
-xref: delta_avge_mass "120.1055"
-xref: delta_composition "H(4) C(7) O(2)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2012-08-01 14:45:32"
-xref: date_time_modified "2012-08-03 09:20:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1348
-name: Cy3-maleimide
-def: "Cy3 Maleimide mono-Reactive dye." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1348]
-synonym: "Cy3 mono-functional maleimides are used for the selective labeling of molecules containing free sulfhydryl groups, such as cysteine residues in proteins and peptides and oligonucleotides." RELATED []
-xref: record_id "1348"
-xref: delta_mono_mass "753.262796"
-xref: delta_avge_mass "753.9046"
-xref: delta_composition "H(45) C(37) N(4) O(9) S(2)"
-xref: username_of_poster "hbromage"
-xref: group_of_poster ""
-xref: date_time_posted "2012-08-27 21:50:06"
-xref: date_time_modified "2015-01-02 09:46:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1349
-name: benzylguanidine
-def: "Modification of the lysine side chain from NH2 to guanidine with a H removed in favor of a benzyl group." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1349]
-synonym: "adds 132 Da to K side chain" RELATED []
-xref: record_id "1349"
-xref: delta_mono_mass "132.068748"
-xref: delta_avge_mass "132.1625"
-xref: delta_composition "H(8) C(8) N(2)"
-xref: username_of_poster "pepinr"
-xref: group_of_poster ""
-xref: date_time_posted "2012-09-06 17:14:04"
-xref: date_time_modified "2012-09-07 15:15:29"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1350
-name: CarboxymethylDMAP
-def: "A fixed +1 charge tag attached to the N-terminus of peptides." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1350]
-synonym: "Added mass is reduced by 1 H to reflect that first charge state requires no proton addition Replaces one of the N-terminal H atoms with C9H12N2O" RELATED []
-xref: record_id "1350"
-xref: delta_mono_mass "162.079313"
-xref: delta_avge_mass "162.1885"
-xref: delta_composition "H(10) C(9) N(2) O"
-xref: username_of_poster "pepinr"
-xref: group_of_poster ""
-xref: date_time_posted "2012-09-06 17:32:42"
-xref: date_time_modified "2012-09-07 15:19:24"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1355
-name: azole
-def: "Formation of five membered aromatic heterocycle." [PMID:15883371, PMID:8895467, PMID:10200165, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1355]
-xref: record_id "1355"
-xref: delta_mono_mass "-20.026215"
-xref: delta_avge_mass "-20.0312"
-xref: delta_composition "H(-4) O(-1)"
-xref: username_of_poster "jomcintosh"
-xref: group_of_poster ""
-xref: date_time_posted "2012-09-10 17:32:20"
-xref: date_time_modified "2012-09-15 00:33:29"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1356
-name: phosphoRibosyl
-def: "Phosphate-ribosylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1356]
-xref: record_id "1356"
-xref: delta_mono_mass "212.00859"
-xref: delta_avge_mass "212.0945"
-xref: delta_composition "H(9) C(5) O(7) P"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2012-09-19 14:16:08"
-xref: date_time_modified "2024-08-12 09:59:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "E"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "R"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1358
-name: NEM:2H(5)+H2O
-def: "D5 N-ethylmaleimide+water on cysteines." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1358]
-comment: Lab based observation that D5 NEM hydrolyses in an analogous way to NEM.
-synonym: "CysNEM D5 hydrolised" RELATED []
-xref: record_id "1358"
-xref: delta_mono_mass "148.089627"
-xref: delta_avge_mass "148.1714"
-xref: delta_composition "H(4) 2H(5) C(6) N O(3)"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2012-10-16 17:45:04"
-xref: date_time_modified "2012-11-02 16:22:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1363
-name: Crotonyl
-def: "Crotonylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1363]
-xref: record_id "1363"
-xref: delta_mono_mass "68.026215"
-xref: delta_avge_mass "68.074"
-xref: delta_composition "H(4) C(4) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2012-12-24 15:50:10"
-xref: date_time_modified "2024-08-12 09:59:07"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1364
-name: O-Et-N-diMePhospho
-def: "O-ethyl, N-dimethyl phosphate." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1364]
-comment: Adduct formed upon reaction of the organophosphate tabun with the active site serine of serine esterases/proteases such as butyrylcholinestease.
-synonym: "tabun" RELATED []
-xref: record_id "1364"
-xref: delta_mono_mass "135.044916"
-xref: delta_avge_mass "135.1015"
-xref: delta_composition "H(10) C(4) N O(2) P"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2013-01-27 13:26:33"
-xref: date_time_modified "2013-02-07 16:50:38"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1365
-name: N-dimethylphosphate
-def: "N-dimethylphosphate." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1365]
-comment: This adduct is a consequence of hydrolysis of the initial adduct formed by tabun (aging) on the active site serine of serine esterases/proteases such as butyrylcholinesterase.
-synonym: "aged tabun" RELATED []
-xref: record_id "1365"
-xref: delta_mono_mass "107.013615"
-xref: delta_avge_mass "107.0483"
-xref: delta_composition "H(6) C(2) N O(2) P"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2013-01-27 13:36:32"
-xref: date_time_modified "2013-02-07 16:49:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1367
-name: dHex(1)Hex(1)
-def: "Hex1dHex1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1367]
-xref: record_id "1367"
-xref: delta_mono_mass "308.110732"
-xref: delta_avge_mass "308.2818"
-xref: delta_composition "dHex Hex"
-xref: username_of_poster "dfplazag"
-xref: group_of_poster ""
-xref: date_time_posted "2013-02-07 14:29:21"
-xref: date_time_modified "2015-05-01 15:14:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_309_mono_mass "308.110732"
-xref: spec_1_neutral_loss_309_avge_mass "308.2818"
-xref: spec_1_neutral_loss_309_flag "false"
-xref: spec_1_neutral_loss_309_composition "dHex Hex"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_309_mono_mass "308.110732"
-xref: spec_1_neutral_loss_309_avge_mass "308.2818"
-xref: spec_1_neutral_loss_309_flag "false"
-xref: spec_1_neutral_loss_309_composition "dHex Hex"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1368
-name: Methyl:2H(3)+Acetyl:2H(3)
-def: "3-fold methylated lysine labelled with Acetyl_heavy." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1368]
-xref: record_id "1368"
-xref: delta_mono_mass "62.063875"
-xref: delta_avge_mass "62.1002"
-xref: delta_composition "H(-2) 2H(6) C(3) O"
-xref: username_of_poster "Plank"
-xref: group_of_poster ""
-xref: date_time_posted "2013-02-14 16:21:54"
-xref: date_time_modified "2013-02-14 16:21:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1370
-name: Label:2H(3)+Oxidation
-def: "Oxidised 2H(3) labelled Methionine." [URL:http\://www.pil.sdu.dk/silac_intro.htm, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1370]
-synonym: "SILAC" RELATED []
-xref: record_id "1370"
-xref: delta_mono_mass "19.013745"
-xref: delta_avge_mass "19.0179"
-xref: delta_composition "H(-3) 2H(3) O"
-xref: username_of_poster "Plank"
-xref: group_of_poster ""
-xref: date_time_posted "2013-02-14 16:36:56"
-xref: date_time_modified "2013-02-22 12:39:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1371
-name: Trimethyl:2H(9)
-def: "3-fold methylation with deuterated methyl groups." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1371]
-xref: record_id "1371"
-xref: delta_mono_mass "51.103441"
-xref: delta_avge_mass "51.1352"
-xref: delta_composition "H(-3) 2H(9) C(3)"
-xref: username_of_poster "Plank"
-xref: group_of_poster ""
-xref: date_time_posted "2013-02-14 17:14:16"
-xref: date_time_modified "2013-02-22 12:37:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "R"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1372
-name: Acetyl:13C(2)
-def: "Heavy acetylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1372]
-xref: record_id "1372"
-xref: delta_mono_mass "44.017274"
-xref: delta_avge_mass "44.022"
-xref: delta_composition "H(2) 13C(2) O"
-xref: username_of_poster "Plank"
-xref: group_of_poster ""
-xref: date_time_posted "2013-02-14 17:24:23"
-xref: date_time_modified "2013-02-14 17:24:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1375
-name: dHex(1)Hex(2)
-def: "Hex2dHex1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1375]
-xref: record_id "1375"
-xref: delta_mono_mass "470.163556"
-xref: delta_avge_mass "470.4224"
-xref: delta_composition "dHex Hex(2)"
-xref: username_of_poster "dfplazag"
-xref: group_of_poster ""
-xref: date_time_posted "2013-04-10 14:57:30"
-xref: date_time_modified "2015-05-01 15:18:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_471_mono_mass "470.163556"
-xref: spec_1_neutral_loss_471_avge_mass "470.4224"
-xref: spec_1_neutral_loss_471_flag "false"
-xref: spec_1_neutral_loss_471_composition "dHex Hex(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_471_mono_mass "470.163556"
-xref: spec_1_neutral_loss_471_avge_mass "470.4224"
-xref: spec_1_neutral_loss_471_flag "false"
-xref: spec_1_neutral_loss_471_composition "dHex Hex(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1376
-name: dHex(1)Hex(3)
-def: "Hex3dHex1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1376]
-xref: record_id "1376"
-xref: delta_mono_mass "632.216379"
-xref: delta_avge_mass "632.563"
-xref: delta_composition "dHex Hex(3)"
-xref: username_of_poster "dfplazag"
-xref: group_of_poster ""
-xref: date_time_posted "2013-04-10 15:00:23"
-xref: date_time_modified "2015-05-01 15:24:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_633_mono_mass "632.216379"
-xref: spec_1_neutral_loss_633_avge_mass "632.563"
-xref: spec_1_neutral_loss_633_flag "false"
-xref: spec_1_neutral_loss_633_composition "dHex Hex(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_633_mono_mass "632.216379"
-xref: spec_1_neutral_loss_633_avge_mass "632.563"
-xref: spec_1_neutral_loss_633_flag "false"
-xref: spec_1_neutral_loss_633_composition "dHex Hex(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1377
-name: dHex(1)Hex(4)
-def: "Hex4dHex1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1377]
-xref: record_id "1377"
-xref: delta_mono_mass "794.269203"
-xref: delta_avge_mass "794.7036"
-xref: delta_composition "dHex Hex(4)"
-xref: username_of_poster "dfplazag"
-xref: group_of_poster ""
-xref: date_time_posted "2013-04-10 15:01:35"
-xref: date_time_modified "2015-05-01 15:27:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_795_mono_mass "794.269203"
-xref: spec_1_neutral_loss_795_avge_mass "794.7036"
-xref: spec_1_neutral_loss_795_flag "false"
-xref: spec_1_neutral_loss_795_composition "dHex Hex(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_795_mono_mass "794.269203"
-xref: spec_1_neutral_loss_795_avge_mass "794.7036"
-xref: spec_1_neutral_loss_795_flag "false"
-xref: spec_1_neutral_loss_795_composition "dHex Hex(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1378
-name: dHex(1)Hex(5)
-def: "Hex5dHex1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1378]
-xref: record_id "1378"
-xref: delta_mono_mass "956.322026"
-xref: delta_avge_mass "956.8442"
-xref: delta_composition "dHex Hex(5)"
-xref: username_of_poster "dfplazag"
-xref: group_of_poster ""
-xref: date_time_posted "2013-04-10 15:03:12"
-xref: date_time_modified "2015-05-01 15:43:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_957_mono_mass "956.322026"
-xref: spec_1_neutral_loss_957_avge_mass "956.8442"
-xref: spec_1_neutral_loss_957_flag "false"
-xref: spec_1_neutral_loss_957_composition "dHex Hex(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_957_mono_mass "956.322026"
-xref: spec_1_neutral_loss_957_avge_mass "956.8442"
-xref: spec_1_neutral_loss_957_flag "false"
-xref: spec_1_neutral_loss_957_composition "dHex Hex(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1379
-name: dHex(1)Hex(6)
-def: "Hex6dHex1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=6&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1379]
-xref: record_id "1379"
-xref: delta_mono_mass "1118.37485"
-xref: delta_avge_mass "1118.9848"
-xref: delta_composition "dHex Hex(6)"
-xref: username_of_poster "dfplazag"
-xref: group_of_poster ""
-xref: date_time_posted "2013-04-10 15:04:22"
-xref: date_time_modified "2015-05-01 15:44:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1119_mono_mass "1118.37485"
-xref: spec_1_neutral_loss_1119_avge_mass "1118.9848"
-xref: spec_1_neutral_loss_1119_flag "false"
-xref: spec_1_neutral_loss_1119_composition "dHex Hex(6)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1119_mono_mass "1118.37485"
-xref: spec_1_neutral_loss_1119_avge_mass "1118.9848"
-xref: spec_1_neutral_loss_1119_flag "false"
-xref: spec_1_neutral_loss_1119_composition "dHex Hex(6)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1380
-name: methylsulfonylethyl
-def: "Reaction with methyl vinyl sulfone." [PMID:http://www.ncbi.nlm.nih.gov/pubmed/?term=2475130, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1380]
-synonym: "protein alkylation by Michael acceptor methyl vinyl sulfone" RELATED []
-xref: record_id "1380"
-xref: delta_mono_mass "106.00885"
-xref: delta_avge_mass "106.1435"
-xref: delta_composition "H(6) C(3) O(2) S"
-xref: username_of_poster "Kramerh"
-xref: group_of_poster ""
-xref: date_time_posted "2013-04-24 14:30:59"
-xref: date_time_modified "2013-05-02 10:13:32"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1381
-name: ethylsulfonylethyl
-def: "Reaction with ethyl vinyl sulfone." [PMID:http://www.ncbi.nlm.nih.gov/pubmed/2475130, PMID:http://www.ncbi.nlm.nih.gov/pubmed/1242713, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1381]
-synonym: "protein alkylation by Michael acceptor ethyl vinyl sulfone" RELATED []
-xref: record_id "1381"
-xref: delta_mono_mass "120.0245"
-xref: delta_avge_mass "120.1701"
-xref: delta_composition "H(8) C(4) O(2) S"
-xref: username_of_poster "Kramerh"
-xref: group_of_poster ""
-xref: date_time_posted "2013-04-24 14:36:48"
-xref: date_time_modified "2013-04-26 09:25:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1382
-name: phenylsulfonylethyl
-def: "Reaction with phenyl vinyl sulfone." [PMID:http://www.ncbi.nlm.nih.gov/pubmed/18528979, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1382]
-synonym: "protein alkylation by Michael acceptor phenyl vinyl sulfone" RELATED []
-xref: record_id "1382"
-xref: delta_mono_mass "168.0245"
-xref: delta_avge_mass "168.2129"
-xref: delta_composition "H(8) C(8) O(2) S"
-xref: username_of_poster "Kramerh"
-xref: group_of_poster ""
-xref: date_time_posted "2013-04-24 14:41:29"
-xref: date_time_modified "2013-04-26 09:25:21"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1383
-name: PyridoxalPhosphateH2
-def: "PLP bound to lysine reduced by sodium borohydride (NaBH4) to create amine linkage." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1383]
-synonym: "Pyridoxal Phosphate reduced" RELATED []
-xref: record_id "1383"
-xref: delta_mono_mass "231.02966"
-xref: delta_avge_mass "231.1425"
-xref: delta_composition "H(10) C(8) N O(5) P"
-xref: username_of_poster "bphilmus"
-xref: group_of_poster ""
-xref: date_time_posted "2013-04-29 17:33:45"
-xref: date_time_modified "2013-05-03 17:30:38"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "This is a chemical derivatization of the PLP imine with sodium borohydride to reduce imine bound through lysine epsilon amine group to chemical stable amine linkage"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1384
-name: Homocysteic_acid
-def: "Methionine oxidation to homocysteic acid." [PMID:20169556, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1384]
-xref: record_id "1384"
-xref: delta_mono_mass "33.969094"
-xref: delta_avge_mass "33.9716"
-xref: delta_composition "H(-2) C(-1) O(3)"
-xref: username_of_poster "mbern"
-xref: group_of_poster ""
-xref: date_time_posted "2013-05-16 20:08:11"
-xref: date_time_modified "2013-05-31 15:57:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1385
-name: Hydroxamic_acid
-def: "ADP-ribosylation followed by conversion to hydroxamic acid via hydroxylamine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1385]
-synonym: "Conversion of carboxylic acid to hydroxamic acid" RELATED []
-xref: record_id "1385"
-xref: delta_mono_mass "15.010899"
-xref: delta_avge_mass "15.0146"
-xref: delta_composition "H N"
-xref: username_of_poster "mbern"
-xref: group_of_poster ""
-xref: date_time_posted "2013-05-16 20:40:47"
-xref: date_time_modified "2020-03-26 09:49:42"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_misc_notes "From exposure to hydroxylamine (used with TMT)"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_misc_notes "From exposure to hydroxylamine (used with TMT)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1387
-name: 3-phosphoglyceryl
-def: "3-phosphoglyceryl." [PMID:http://www.ncbi.nlm.nih.gov/pubmed/?term=23908237, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1387]
-xref: record_id "1387"
-xref: delta_mono_mass "167.982375"
-xref: delta_avge_mass "168.042"
-xref: delta_composition "H(5) C(3) O(6) P"
-xref: username_of_poster "BThomas"
-xref: group_of_poster ""
-xref: date_time_posted "2013-08-05 10:54:22"
-xref: date_time_modified "2013-11-01 16:34:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1388
-name: HN2_mustard
-def: "Modification by hydroxylated mechloroethamine (HN-2)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1388]
-xref: record_id "1388"
-xref: delta_mono_mass "101.084064"
-xref: delta_avge_mass "101.1469"
-xref: delta_composition "H(11) C(5) N O"
-xref: username_of_poster "vthompson"
-xref: group_of_poster ""
-xref: date_time_posted "2013-08-23 18:36:39"
-xref: date_time_modified "2013-09-23 11:42:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1389
-name: HN3_mustard
-def: "Modification by hydroxylated tris-(2-chloroethyl)amine (HN-3)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1389]
-xref: record_id "1389"
-xref: delta_mono_mass "131.094629"
-xref: delta_avge_mass "131.1729"
-xref: delta_composition "H(13) C(6) N O(2)"
-xref: username_of_poster "vthompson"
-xref: group_of_poster ""
-xref: date_time_posted "2013-08-23 19:13:36"
-xref: date_time_modified "2013-09-23 11:42:08"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1390
-name: Oxidation+NEM
-def: "N-ethylmaleimide on cysteine sulfenic acid." [PMID:24103186, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1390]
-xref: record_id "1390"
-xref: delta_mono_mass "141.042593"
-xref: delta_avge_mass "141.1247"
-xref: delta_composition "H(7) C(6) N O(3)"
-xref: username_of_poster "jheld"
-xref: group_of_poster ""
-xref: date_time_posted "2013-10-16 15:31:20"
-xref: date_time_modified "2013-11-01 16:37:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1391
-name: NHS-fluorescein
-def: "Fluorescein-hexanoate-NHS hydrolysis." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1391]
-xref: record_id "1391"
-xref: delta_mono_mass "471.131802"
-xref: delta_avge_mass "471.4581"
-xref: delta_composition "H(21) C(27) N O(7)"
-xref: username_of_poster "cgadelha"
-xref: group_of_poster ""
-xref: date_time_posted "2013-10-18 12:14:19"
-xref: date_time_modified "2013-11-01 16:37:42"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1392
-name: DiART6plex
-def: "Representative mass and accurate mass for 114." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1392]
-comment: Different tags have the same nominal mass but slightly different exact masses. Use this modification for all tags for quantitation purposes. Monoisotopic masses of the fragment ions to be quantified are 114.12827, 115.12531, 116.14082, 117.13786, 118.14752, 119.14456.
-synonym: "Isobaric labeling reagent from Omic Biosystems, Inc. AKA DiART6plex114" RELATED []
-xref: record_id "1392"
-xref: delta_mono_mass "217.162932"
-xref: delta_avge_mass "217.2527"
-xref: delta_composition "H(20) C(7) 13C(4) N 15N O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2013-11-06 11:18:58"
-xref: date_time_modified "2016-09-22 14:39:36"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Isotopic label"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "Y"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "Low abundance"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1393
-name: DiART6plex115
-def: "Accurate mass for DiART6plex 115." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1393]
-comment: Different tags have the same nominal mass but slightly different exact masses.
-synonym: "Isobaric labeling reagent from Omic Biosystems, Inc." RELATED []
-xref: record_id "1393"
-xref: delta_mono_mass "217.156612"
-xref: delta_avge_mass "217.2535"
-xref: delta_composition "H(20) C(8) 13C(3) 15N(2) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2013-11-06 11:34:33"
-xref: date_time_modified "2013-11-06 11:34:33"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Isotopic label"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "Y"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "Low abundance"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1394
-name: DiART6plex116/119
-def: "Accurate mass for DiART6plex 116 and 119." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1394]
-comment: Different tags have the same nominal mass but slightly different exact masses.
-synonym: "Isobaric labeling reagent from Omic Biosystems, Inc." RELATED []
-xref: record_id "1394"
-xref: delta_mono_mass "217.168776"
-xref: delta_avge_mass "217.2797"
-xref: delta_composition "H(18) 2H(2) C(9) 13C(2) N 15N O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2013-11-06 11:35:52"
-xref: date_time_modified "2013-11-06 11:38:53"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Isotopic label"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "Y"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "Low abundance"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1395
-name: DiART6plex117
-def: "Accurate mass for DiART6plex 117." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1395]
-comment: Different tags have the same nominal mass but slightly different exact masses.
-synonym: "Isobaric labeling reagent from Omic Biosystems, Inc." RELATED []
-xref: record_id "1395"
-xref: delta_mono_mass "217.162456"
-xref: delta_avge_mass "217.2805"
-xref: delta_composition "H(18) 2H(2) C(10) 13C 15N(2) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2013-11-06 11:40:01"
-xref: date_time_modified "2013-11-06 11:40:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Isotopic label"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "Y"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "Low abundance"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1396
-name: DiART6plex118
-def: "Accurate mass for DiART6plex 118." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1396]
-comment: Different tags have the same nominal mass but slightly different exact masses.
-synonym: "Isobaric labeling reagent from Omic Biosystems, Inc." RELATED []
-xref: record_id "1396"
-xref: delta_mono_mass "217.175096"
-xref: delta_avge_mass "217.279"
-xref: delta_composition "H(18) 2H(2) C(8) 13C(3) N(2) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2013-11-06 11:40:58"
-xref: date_time_modified "2013-11-06 11:40:58"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Isotopic label"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "Y"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_4_misc_notes "Low abundance"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1397
-name: Iodoacetanilide
-def: "Iodoacetanilide derivative." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1397]
-xref: record_id "1397"
-xref: delta_mono_mass "133.052764"
-xref: delta_avge_mass "133.1473"
-xref: delta_composition "H(7) C(8) N O"
-xref: username_of_poster "kcook123"
-xref: group_of_poster ""
-xref: date_time_posted "2013-12-10 04:26:07"
-xref: date_time_modified "2014-03-01 17:35:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1398
-name: Iodoacetanilide:13C(6)
-def: "13C labelled iodoacetanilide derivative." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1398]
-xref: record_id "1398"
-xref: delta_mono_mass "139.072893"
-xref: delta_avge_mass "139.1032"
-xref: delta_composition "H(7) C(2) 13C(6) N O"
-xref: username_of_poster "kcook123"
-xref: group_of_poster ""
-xref: date_time_posted "2013-12-10 04:31:00"
-xref: date_time_modified "2014-03-01 17:36:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1399
-name: Dap-DSP
-def: "Diaminopimelic acid-DSP monolinked." [URL:https\://tools.thermofisher.com/content/sfs/manuals/MAN0011280_DTSSP_DSP_UG.pdf, URL:https\://www.ncbi.nlm.nih.gov/pubmed/?term=322714, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1399]
-comment: Addition of gram negative peptidoglycan amino acid (DAP) plus monolinked DSP.
-xref: record_id "1399"
-xref: delta_mono_mass "364.076278"
-xref: delta_avge_mass "364.4377"
-xref: delta_composition "H(20) C(13) N(2) O(6) S(2)"
-xref: username_of_poster "grigorios"
-xref: group_of_poster ""
-xref: date_time_posted "2014-02-20 11:23:24"
-xref: date_time_modified "2017-09-19 11:06:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Non-standard residue"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "E"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Non-standard residue"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1400
-name: MurNAc
-def: "N-Acetylmuramic acid." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1400]
-comment: Gram negative peptidoglycan saccharide amide bonded to Alanine.
-xref: record_id "1400"
-xref: delta_mono_mass "275.100502"
-xref: delta_avge_mass "275.2552"
-xref: delta_composition "O(-1) NeuAc"
-xref: username_of_poster "grigorios"
-xref: group_of_poster ""
-xref: date_time_posted "2014-02-20 12:47:46"
-xref: date_time_modified "2015-05-01 13:37:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other glycosylation"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1402
-name: Label:2H(7)15N(4)
-def: "Label:2H(7)15N(4)." [URL:http\://shop.isotope.com/productdetails.aspx?id=10032309&itemno=DNLM-7543-PK, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1402]
-comment: For SILAC experiments.
-synonym: "Cambridge Isotopes DNLM-7543-PK" RELATED []
-xref: record_id "1402"
-xref: delta_mono_mass "11.032077"
-xref: delta_avge_mass "11.0168"
-xref: delta_composition "H(-7) 2H(7) N(-4) 15N(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2014-04-16 12:16:45"
-xref: date_time_modified "2014-04-16 12:16:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1403
-name: Label:2H(6)15N(1)
-def: "Label:2H(6)15N(1)." [URL:http\://shop.isotope.com/productdetails.aspx?id=10032309&itemno=DNLM-7543-PK, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1403]
-comment: For SILAC experiments.
-synonym: "Arg-Pro conversion of Label:2H(7)15N(4)" RELATED []
-xref: record_id "1403"
-xref: delta_mono_mass "7.034695"
-xref: delta_avge_mass "7.0304"
-xref: delta_composition "H(-6) 2H(6) N(-1) 15N"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2014-04-16 12:19:06"
-xref: date_time_modified "2014-04-16 12:19:06"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1405
-name: EEEDVIEVYQEQTGG
-def: "Sumoylation by SUMO-1 after Cyanogen bromide (CNBr) cleavage." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1405]
-xref: record_id "1405"
-xref: delta_mono_mass "1705.73189"
-xref: delta_avge_mass "1706.7153"
-xref: delta_composition "H(107) C(72) N(17) O(31)"
-xref: username_of_poster "vogelw"
-xref: group_of_poster ""
-xref: date_time_posted "2014-06-25 15:15:44"
-xref: date_time_modified "2014-08-08 11:37:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1406
-name: EDEDTIDVFQQQTGG
-def: "Sumoylation by SUMO-2/3 after Cyanogen bromide (CNBr) cleavage." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1406]
-xref: record_id "1406"
-xref: delta_mono_mass "1662.700924"
-xref: delta_avge_mass "1663.6508"
-xref: delta_composition "H(102) C(69) N(18) O(30)"
-xref: username_of_poster "vogelw"
-xref: group_of_poster ""
-xref: date_time_posted "2014-06-25 15:19:11"
-xref: date_time_modified "2014-08-08 11:37:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "The cleavage products of SUMO-2 and SUMO-3 are indistinguishable"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1408
-name: Hex(5)HexNAc(4)NeuAc(2)
-def: "A2G2S2/G2S2." [URL:http\://www.unicarbkb.org/structure/1187, URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=5&hexnac=4&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1408]
-xref: record_id "1408"
-xref: delta_mono_mass "2204.772441"
-xref: delta_avge_mass "2205.9822"
-xref: delta_composition "Hex(5) HexNAc(4) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2014-07-31 13:51:41"
-xref: date_time_modified "2020-08-02 11:36:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_2205_mono_mass "2204.772441"
-xref: spec_1_neutral_loss_2205_avge_mass "2205.9822"
-xref: spec_1_neutral_loss_2205_flag "false"
-xref: spec_1_neutral_loss_2205_composition "Hex(5) HexNAc(4) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1409
-name: Hex(5)HexNAc(4)NeuAc(1)
-def: "A2G2S1/G2S1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=5&hexnac=4&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1409]
-xref: record_id "1409"
-xref: delta_mono_mass "1913.677025"
-xref: delta_avge_mass "1914.7277"
-xref: delta_composition "Hex(5) HexNAc(4) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2014-07-31 13:52:20"
-xref: date_time_modified "2020-08-02 11:37:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1914_mono_mass "1913.677025"
-xref: spec_1_neutral_loss_1914_avge_mass "1914.7277"
-xref: spec_1_neutral_loss_1914_flag "false"
-xref: spec_1_neutral_loss_1914_composition "Hex(5) HexNAc(4) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1410
-name: dHex(1)Hex(5)HexNAc(4)NeuAc(1)
-def: "FA2G2S1/G2FS1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=5&hexnac=4&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1410]
-xref: record_id "1410"
-xref: delta_mono_mass "2059.734933"
-xref: delta_avge_mass "2060.8689"
-xref: delta_composition "dHex Hex(5) HexNAc(4) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2014-07-31 13:53:31"
-xref: date_time_modified "2020-08-02 11:40:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_2060_mono_mass "2059.734933"
-xref: spec_1_neutral_loss_2060_avge_mass "2060.8689"
-xref: spec_1_neutral_loss_2060_flag "false"
-xref: spec_1_neutral_loss_2060_composition "dHex Hex(5) HexNAc(4) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1411
-name: dHex(1)Hex(5)HexNAc(4)NeuAc(2)
-def: "FA2G2S2/G2FS2." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=5&hexnac=4&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1411]
-xref: record_id "1411"
-xref: delta_mono_mass "2350.83035"
-xref: delta_avge_mass "2352.1234"
-xref: delta_composition "dHex Hex(5) HexNAc(4) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2014-07-31 13:53:47"
-xref: date_time_modified "2020-08-02 11:40:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_2351_mono_mass "2350.83035"
-xref: spec_1_neutral_loss_2351_avge_mass "2352.1234"
-xref: spec_1_neutral_loss_2351_flag "false"
-xref: spec_1_neutral_loss_2351_composition "dHex Hex(5) HexNAc(4) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1412
-name: s-GlcNAc
-def: "O3S1HexNAc1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1412]
-xref: record_id "1412"
-xref: delta_mono_mass "283.036187"
-xref: delta_avge_mass "283.2557"
-xref: delta_composition "O(3) S HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2014-08-14 15:34:42"
-xref: date_time_modified "2015-05-01 15:10:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_284_mono_mass "283.036187"
-xref: spec_1_neutral_loss_284_avge_mass "283.2557"
-xref: spec_1_neutral_loss_284_flag "false"
-xref: spec_1_neutral_loss_284_composition "O(3) S HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_284_mono_mass "283.036187"
-xref: spec_1_neutral_loss_284_avge_mass "283.2557"
-xref: spec_1_neutral_loss_284_flag "false"
-xref: spec_1_neutral_loss_284_composition "O(3) S HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1413
-name: PhosphoHex(2)
-def: "H1O3P1Hex2." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=1&hex=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1413]
-xref: record_id "1413"
-xref: delta_mono_mass "404.071978"
-xref: delta_avge_mass "404.2611"
-xref: delta_composition "H O(3) P Hex(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2014-08-14 15:38:35"
-xref: date_time_modified "2017-11-23 15:44:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_405_mono_mass "404.071978"
-xref: spec_1_neutral_loss_405_avge_mass "404.2611"
-xref: spec_1_neutral_loss_405_flag "false"
-xref: spec_1_neutral_loss_405_composition "H O(3) P Hex(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_405_mono_mass "404.071978"
-xref: spec_1_neutral_loss_405_avge_mass "404.2611"
-xref: spec_1_neutral_loss_405_flag "false"
-xref: spec_1_neutral_loss_405_composition "H O(3) P Hex(2)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_misc_notes "Not reported for human proteins"
-xref: spec_2_neutral_loss_405_mono_mass "404.071978"
-xref: spec_2_neutral_loss_405_avge_mass "404.2611"
-xref: spec_2_neutral_loss_405_flag "false"
-xref: spec_2_neutral_loss_405_composition "H O(3) P Hex(2)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1414
-name: Trimethyl:13C(3)2H(9)
-def: "3-fold methylation with fully labelled methyl groups." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1414]
-xref: record_id "1414"
-xref: delta_mono_mass "54.113505"
-xref: delta_avge_mass "54.1132"
-xref: delta_composition "H(-3) 2H(9) 13C(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2014-09-17 09:18:49"
-xref: date_time_modified "2014-09-17 09:18:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "R"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1419
-name: 15N-oxobutanoic
-def: "Loss of ammonia (15N)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1419]
-synonym: "pyruvic acid from N-term ser oxobutanoic acid from N term Thr" RELATED []
-xref: record_id "1419"
-xref: delta_mono_mass "-18.023584"
-xref: delta_avge_mass "-18.0239"
-xref: delta_composition "H(-3) 15N(-1)"
-xref: username_of_poster "fufezan"
-xref: group_of_poster ""
-xref: date_time_posted "2014-11-24 13:24:53"
-xref: date_time_modified "2015-01-12 16:11:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Artefact"
-xref: spec_1_misc_notes "Pyro-carbamidomethyl as a delta from Carbamidomethyl-Cys"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1420
-name: spermine
-def: "Spermine adduct." [URL:http\://dx.doi.org/10.1007/s00726-014-1879-8, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1420]
-xref: record_id "1420"
-xref: delta_mono_mass "185.189198"
-xref: delta_avge_mass "185.3097"
-xref: delta_composition "H(23) C(10) N(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-01-12 16:07:00"
-xref: date_time_modified "2024-08-12 10:11:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1421
-name: spermidine
-def: "Spermidine adduct." [URL:http\://dx.doi.org/10.1007/s00726-014-1879-8, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1421]
-xref: record_id "1421"
-xref: delta_mono_mass "128.131349"
-xref: delta_avge_mass "128.2153"
-xref: delta_composition "H(16) C(7) N(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-01-12 16:08:04"
-xref: date_time_modified "2024-08-12 10:11:10"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1423
-name: Biotin:Thermo-21330
-def: "Biotin_PEG4." [URL:http\://www.lifetechnologies.com/order/catalog/product/21330, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1423]
-comment: Also available as 21329, 21362, 21363.
-synonym: "NHS-PEG4-Biotin" RELATED []
-xref: record_id "1423"
-xref: delta_mono_mass "473.219571"
-xref: delta_avge_mass "473.5835"
-xref: delta_composition "H(35) C(21) N(3) O(7) S"
-xref: username_of_poster "rbomgard"
-xref: group_of_poster ""
-xref: date_time_posted "2015-04-20 16:08:05"
-xref: date_time_modified "2015-04-20 16:10:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1425
-name: Pentose
-def: "Pentose." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1425]
-xref: record_id "1425"
-xref: delta_mono_mass "132.042259"
-xref: delta_avge_mass "132.1146"
-xref: delta_composition "Pent"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-01 17:01:09"
-xref: date_time_modified "2015-05-05 10:48:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_133_mono_mass "132.042259"
-xref: spec_1_neutral_loss_133_avge_mass "132.1146"
-xref: spec_1_neutral_loss_133_flag "false"
-xref: spec_1_neutral_loss_133_composition "Pent"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_133_mono_mass "132.042259"
-xref: spec_1_neutral_loss_133_avge_mass "132.1146"
-xref: spec_1_neutral_loss_133_flag "false"
-xref: spec_1_neutral_loss_133_composition "Pent"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1426
-name: Hex(1)Pent(1)
-def: "Hex Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?pent=1&hex=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1426]
-xref: record_id "1426"
-xref: delta_mono_mass "294.095082"
-xref: delta_avge_mass "294.2552"
-xref: delta_composition "Pent Hex"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-01 17:03:00"
-xref: date_time_modified "2015-05-05 10:49:06"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_295_mono_mass "294.095082"
-xref: spec_1_neutral_loss_295_avge_mass "294.2552"
-xref: spec_1_neutral_loss_295_flag "false"
-xref: spec_1_neutral_loss_295_composition "Pent Hex"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_295_mono_mass "294.095082"
-xref: spec_1_neutral_loss_295_avge_mass "294.2552"
-xref: spec_1_neutral_loss_295_flag "false"
-xref: spec_1_neutral_loss_295_composition "Pent Hex"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1427
-name: Hex(1)HexA(1)
-def: "Hex HexA." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexa=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1427]
-xref: record_id "1427"
-xref: delta_mono_mass "338.084912"
-xref: delta_avge_mass "338.2647"
-xref: delta_composition "Hex HexA"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-01 17:05:51"
-xref: date_time_modified "2015-05-05 10:49:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_339_mono_mass "338.084912"
-xref: spec_1_neutral_loss_339_avge_mass "338.2647"
-xref: spec_1_neutral_loss_339_flag "false"
-xref: spec_1_neutral_loss_339_composition "Hex HexA"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_339_mono_mass "338.084912"
-xref: spec_1_neutral_loss_339_avge_mass "338.2647"
-xref: spec_1_neutral_loss_339_flag "false"
-xref: spec_1_neutral_loss_339_composition "Hex HexA"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1428
-name: Hex(1)Pent(2)
-def: "Hex Pent(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?pent=2&hex=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1428]
-xref: record_id "1428"
-xref: delta_mono_mass "426.137341"
-xref: delta_avge_mass "426.3698"
-xref: delta_composition "Pent(2) Hex"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 09:37:19"
-xref: date_time_modified "2015-05-05 10:50:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_427_mono_mass "426.137341"
-xref: spec_1_neutral_loss_427_avge_mass "426.3698"
-xref: spec_1_neutral_loss_427_flag "false"
-xref: spec_1_neutral_loss_427_composition "Pent(2) Hex"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_427_mono_mass "426.137341"
-xref: spec_1_neutral_loss_427_avge_mass "426.3698"
-xref: spec_1_neutral_loss_427_flag "false"
-xref: spec_1_neutral_loss_427_composition "Pent(2) Hex"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1429
-name: Hex(1)HexNAc(1)Phos(1)
-def: "Hex HexNAc Phos." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=1&hex=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1429]
-xref: record_id "1429"
-xref: delta_mono_mass "445.098527"
-xref: delta_avge_mass "445.313"
-xref: delta_composition "H O(3) P Hex HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 09:40:49"
-xref: date_time_modified "2015-05-06 12:07:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_446_mono_mass "445.098527"
-xref: spec_1_neutral_loss_446_avge_mass "445.313"
-xref: spec_1_neutral_loss_446_flag "false"
-xref: spec_1_neutral_loss_446_composition "H O(3) P Hex HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_446_mono_mass "445.098527"
-xref: spec_1_neutral_loss_446_avge_mass "445.313"
-xref: spec_1_neutral_loss_446_flag "false"
-xref: spec_1_neutral_loss_446_composition "H O(3) P Hex HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1430
-name: Hex(1)HexNAc(1)Sulf(1)
-def: "Hex HexNAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1430]
-xref: record_id "1430"
-xref: delta_mono_mass "445.089011"
-xref: delta_avge_mass "445.3963"
-xref: delta_composition "O(3) S Hex HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 09:41:48"
-xref: date_time_modified "2015-05-06 12:07:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_446_mono_mass "445.089011"
-xref: spec_1_neutral_loss_446_avge_mass "445.3963"
-xref: spec_1_neutral_loss_446_flag "false"
-xref: spec_1_neutral_loss_446_composition "O(3) S Hex HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_446_mono_mass "445.089011"
-xref: spec_1_neutral_loss_446_avge_mass "445.3963"
-xref: spec_1_neutral_loss_446_flag "false"
-xref: spec_1_neutral_loss_446_composition "O(3) S Hex HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1431
-name: Hex(1)NeuAc(1)
-def: "Hex NeuAc ---OR--- HexNAc Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1431]
-xref: record_id "1431"
-xref: delta_mono_mass "453.14824"
-xref: delta_avge_mass "453.3952"
-xref: delta_composition "Hex NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 09:45:11"
-xref: date_time_modified "2017-11-17 11:42:48"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_454_mono_mass "453.14824"
-xref: spec_1_neutral_loss_454_avge_mass "453.3952"
-xref: spec_1_neutral_loss_454_flag "false"
-xref: spec_1_neutral_loss_454_composition "Hex NeuAc"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_454_mono_mass "453.14824"
-xref: spec_1_neutral_loss_454_avge_mass "453.3952"
-xref: spec_1_neutral_loss_454_flag "false"
-xref: spec_1_neutral_loss_454_composition "Hex NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1432
-name: Hex(1)NeuGc(1)
-def: "Hex NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1432]
-xref: record_id "1432"
-xref: delta_mono_mass "469.143155"
-xref: delta_avge_mass "469.3946"
-xref: delta_composition "Hex NeuGc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 09:45:57"
-xref: date_time_modified "2015-05-05 10:51:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_470_mono_mass "469.143155"
-xref: spec_1_neutral_loss_470_avge_mass "469.3946"
-xref: spec_1_neutral_loss_470_flag "false"
-xref: spec_1_neutral_loss_470_composition "Hex NeuGc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_470_mono_mass "469.143155"
-xref: spec_1_neutral_loss_470_avge_mass "469.3946"
-xref: spec_1_neutral_loss_470_flag "false"
-xref: spec_1_neutral_loss_470_composition "Hex NeuGc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1433
-name: HexNAc(3)
-def: "HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1433]
-xref: record_id "1433"
-xref: delta_mono_mass "609.238118"
-xref: delta_avge_mass "609.5776"
-xref: delta_composition "HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 09:47:58"
-xref: date_time_modified "2015-05-06 12:09:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_610_mono_mass "609.238118"
-xref: spec_1_neutral_loss_610_avge_mass "609.5776"
-xref: spec_1_neutral_loss_610_flag "false"
-xref: spec_1_neutral_loss_610_composition "HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_610_mono_mass "609.238118"
-xref: spec_1_neutral_loss_610_avge_mass "609.5776"
-xref: spec_1_neutral_loss_610_flag "false"
-xref: spec_1_neutral_loss_610_composition "HexNAc(3)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1434
-name: HexNAc(1)NeuAc(1)
-def: "HexNAc NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hexnac=1&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1434]
-xref: record_id "1434"
-xref: delta_mono_mass "494.174789"
-xref: delta_avge_mass "494.4471"
-xref: delta_composition "HexNAc NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 09:53:18"
-xref: date_time_modified "2015-05-05 10:52:24"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_495_mono_mass "494.174789"
-xref: spec_1_neutral_loss_495_avge_mass "494.4471"
-xref: spec_1_neutral_loss_495_flag "false"
-xref: spec_1_neutral_loss_495_composition "HexNAc NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_495_mono_mass "494.174789"
-xref: spec_1_neutral_loss_495_avge_mass "494.4471"
-xref: spec_1_neutral_loss_495_flag "false"
-xref: spec_1_neutral_loss_495_composition "HexNAc NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1435
-name: HexNAc(1)NeuGc(1)
-def: "HexNAc NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hexnac=1&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1435]
-xref: record_id "1435"
-xref: delta_mono_mass "510.169704"
-xref: delta_avge_mass "510.4465"
-xref: delta_composition "HexNAc NeuGc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 09:54:16"
-xref: date_time_modified "2015-05-05 10:52:39"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_511_mono_mass "510.169704"
-xref: spec_1_neutral_loss_511_avge_mass "510.4465"
-xref: spec_1_neutral_loss_511_flag "false"
-xref: spec_1_neutral_loss_511_composition "HexNAc NeuGc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_511_mono_mass "510.169704"
-xref: spec_1_neutral_loss_511_avge_mass "510.4465"
-xref: spec_1_neutral_loss_511_flag "false"
-xref: spec_1_neutral_loss_511_composition "HexNAc NeuGc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1436
-name: Hex(1)HexNAc(1)dHex(1)Me(1)
-def: "Hex HexNAc dHex Me." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?methyl=1&dhex=1&hex=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1436]
-xref: record_id "1436"
-xref: delta_mono_mass "525.205755"
-xref: delta_avge_mass "525.5009"
-xref: delta_composition "Me dHex Hex HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 10:05:16"
-xref: date_time_modified "2015-05-06 12:08:10"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_526_mono_mass "525.205755"
-xref: spec_1_neutral_loss_526_avge_mass "525.5009"
-xref: spec_1_neutral_loss_526_flag "false"
-xref: spec_1_neutral_loss_526_composition "Me dHex Hex HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_526_mono_mass "525.205755"
-xref: spec_1_neutral_loss_526_avge_mass "525.5009"
-xref: spec_1_neutral_loss_526_flag "false"
-xref: spec_1_neutral_loss_526_composition "Me dHex Hex HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1437
-name: Hex(1)HexNAc(1)dHex(1)Me(2)
-def: "Hex HexNAc dHex Me(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?methyl=2&dhex=1&hex=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1437]
-xref: record_id "1437"
-xref: delta_mono_mass "539.221405"
-xref: delta_avge_mass "539.5275"
-xref: delta_composition "Me(2) dHex Hex HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 10:06:28"
-xref: date_time_modified "2015-05-06 12:08:43"
-xref: approved "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_540_mono_mass "539.221405"
-xref: spec_2_neutral_loss_540_avge_mass "539.5275"
-xref: spec_2_neutral_loss_540_flag "false"
-xref: spec_2_neutral_loss_540_composition "Me(2) dHex Hex HexNAc"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_540_mono_mass "539.221405"
-xref: spec_2_neutral_loss_540_avge_mass "539.5275"
-xref: spec_2_neutral_loss_540_flag "false"
-xref: spec_2_neutral_loss_540_composition "Me(2) dHex Hex HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1438
-name: Hex(2)HexNAc(1)
-def: "Hex(2) HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1438]
-xref: record_id "1438"
-xref: delta_mono_mass "527.18502"
-xref: delta_avge_mass "527.4737"
-xref: delta_composition "Hex(2) HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 10:09:00"
-xref: date_time_modified "2017-11-23 16:36:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_528_mono_mass "527.18502"
-xref: spec_1_neutral_loss_528_avge_mass "527.4737"
-xref: spec_1_neutral_loss_528_flag "false"
-xref: spec_1_neutral_loss_528_composition "Hex(2) HexNAc"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_528_mono_mass "527.18502"
-xref: spec_1_neutral_loss_528_avge_mass "527.4737"
-xref: spec_1_neutral_loss_528_flag "false"
-xref: spec_1_neutral_loss_528_composition "Hex(2) HexNAc"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_528_mono_mass "527.18502"
-xref: spec_2_neutral_loss_528_avge_mass "527.4737"
-xref: spec_2_neutral_loss_528_flag "false"
-xref: spec_2_neutral_loss_528_composition "Hex(2) HexNAc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1439
-name: Hex(1)HexA(1)HexNAc(1)
-def: "Hex HexA HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexa=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1439]
-xref: record_id "1439"
-xref: delta_mono_mass "541.164284"
-xref: delta_avge_mass "541.4572"
-xref: delta_composition "Hex HexA HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 10:10:30"
-xref: date_time_modified "2015-05-05 10:55:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_542_mono_mass "541.164284"
-xref: spec_1_neutral_loss_542_avge_mass "541.4572"
-xref: spec_1_neutral_loss_542_flag "false"
-xref: spec_1_neutral_loss_542_composition "Hex HexA HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_542_mono_mass "541.164284"
-xref: spec_1_neutral_loss_542_avge_mass "541.4572"
-xref: spec_1_neutral_loss_542_flag "false"
-xref: spec_1_neutral_loss_542_composition "Hex HexA HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1440
-name: Hex(2)HexNAc(1)Me(1)
-def: "Hex(2) HexNAc Me." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?methyl=1&hex=2&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1440]
-xref: record_id "1440"
-xref: delta_mono_mass "541.20067"
-xref: delta_avge_mass "541.5003"
-xref: delta_composition "Me Hex(2) HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 10:12:19"
-xref: date_time_modified "2015-05-06 12:08:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_542_mono_mass "541.20067"
-xref: spec_1_neutral_loss_542_avge_mass "541.5003"
-xref: spec_1_neutral_loss_542_flag "false"
-xref: spec_1_neutral_loss_542_composition "Me Hex(2) HexNAc"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_542_mono_mass "541.20067"
-xref: spec_1_neutral_loss_542_avge_mass "541.5003"
-xref: spec_1_neutral_loss_542_flag "false"
-xref: spec_1_neutral_loss_542_composition "Me Hex(2) HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1441
-name: Hex(1)Pent(3)
-def: "Hex Pent(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?pent=3&hex=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1441]
-xref: record_id "1441"
-xref: delta_mono_mass "558.1796"
-xref: delta_avge_mass "558.4845"
-xref: delta_composition "Pent(3) Hex"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 10:14:37"
-xref: date_time_modified "2017-11-23 16:39:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_559_mono_mass "558.1796"
-xref: spec_1_neutral_loss_559_avge_mass "558.4845"
-xref: spec_1_neutral_loss_559_flag "false"
-xref: spec_1_neutral_loss_559_composition "Pent(3) Hex"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_559_mono_mass "558.1796"
-xref: spec_1_neutral_loss_559_avge_mass "558.4845"
-xref: spec_1_neutral_loss_559_flag "false"
-xref: spec_1_neutral_loss_559_composition "Pent(3) Hex"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1442
-name: Hex(1)NeuAc(1)Pent(1)
-def: "Hex NeuAc Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?pent=1&hex=1&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1442]
-xref: record_id "1442"
-xref: delta_mono_mass "585.190499"
-xref: delta_avge_mass "585.5098"
-xref: delta_composition "Pent Hex NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 10:59:44"
-xref: date_time_modified "2015-05-05 10:59:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_586_mono_mass "585.190499"
-xref: spec_1_neutral_loss_586_avge_mass "585.5098"
-xref: spec_1_neutral_loss_586_flag "false"
-xref: spec_1_neutral_loss_586_composition "Pent Hex NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_586_mono_mass "585.190499"
-xref: spec_1_neutral_loss_586_avge_mass "585.5098"
-xref: spec_1_neutral_loss_586_flag "false"
-xref: spec_1_neutral_loss_586_composition "Pent Hex NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1443
-name: Hex(2)HexNAc(1)Sulf(1)
-def: "Hex(2) HexNAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=2&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1443]
-xref: record_id "1443"
-xref: delta_mono_mass "607.141834"
-xref: delta_avge_mass "607.5369"
-xref: delta_composition "O(3) S Hex(2) HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 11:01:43"
-xref: date_time_modified "2015-05-06 12:09:15"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_608_mono_mass "607.141834"
-xref: spec_1_neutral_loss_608_avge_mass "607.5369"
-xref: spec_1_neutral_loss_608_flag "false"
-xref: spec_1_neutral_loss_608_composition "O(3) S Hex(2) HexNAc"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_608_mono_mass "607.141834"
-xref: spec_1_neutral_loss_608_avge_mass "607.5369"
-xref: spec_1_neutral_loss_608_flag "false"
-xref: spec_1_neutral_loss_608_composition "O(3) S Hex(2) HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1444
-name: Hex(2)NeuAc(1)
-def: "Hex(2) NeuAc ---OR--- Hex HexNAc Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1444]
-xref: record_id "1444"
-xref: delta_mono_mass "615.201064"
-xref: delta_avge_mass "615.5358"
-xref: delta_composition "Hex(2) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 11:04:03"
-xref: date_time_modified "2017-11-17 11:43:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_616_mono_mass "615.201064"
-xref: spec_1_neutral_loss_616_avge_mass "615.5358"
-xref: spec_1_neutral_loss_616_flag "false"
-xref: spec_1_neutral_loss_616_composition "Hex(2) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_616_mono_mass "615.201064"
-xref: spec_1_neutral_loss_616_avge_mass "615.5358"
-xref: spec_1_neutral_loss_616_flag "false"
-xref: spec_1_neutral_loss_616_composition "Hex(2) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1445
-name: dHex(2)Hex(2)
-def: "Hex2 dHex2." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1445]
-xref: record_id "1445"
-xref: delta_mono_mass "616.221465"
-xref: delta_avge_mass "616.5636"
-xref: delta_composition "dHex(2) Hex(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 11:05:19"
-xref: date_time_modified "2015-05-05 11:05:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_617_mono_mass "616.221465"
-xref: spec_1_neutral_loss_617_avge_mass "616.5636"
-xref: spec_1_neutral_loss_617_flag "false"
-xref: spec_1_neutral_loss_617_composition "dHex(2) Hex(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_617_mono_mass "616.221465"
-xref: spec_1_neutral_loss_617_avge_mass "616.5636"
-xref: spec_1_neutral_loss_617_flag "false"
-xref: spec_1_neutral_loss_617_composition "dHex(2) Hex(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1446
-name: dHex(1)Hex(2)HexA(1)
-def: "DHex Hex(2) HexA." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=2&hexa=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1446]
-xref: record_id "1446"
-xref: delta_mono_mass "646.195644"
-xref: delta_avge_mass "646.5465"
-xref: delta_composition "dHex Hex(2) HexA"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 11:06:47"
-xref: date_time_modified "2015-05-05 11:06:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_647_mono_mass "646.195644"
-xref: spec_1_neutral_loss_647_avge_mass "646.5465"
-xref: spec_1_neutral_loss_647_flag "false"
-xref: spec_1_neutral_loss_647_composition "dHex Hex(2) HexA"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_647_mono_mass "646.195644"
-xref: spec_1_neutral_loss_647_avge_mass "646.5465"
-xref: spec_1_neutral_loss_647_flag "false"
-xref: spec_1_neutral_loss_647_composition "dHex Hex(2) HexA"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1447
-name: Hex(1)HexNAc(2)Sulf(1)
-def: "Hex HexNAc(2) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1447]
-xref: record_id "1447"
-xref: delta_mono_mass "648.168383"
-xref: delta_avge_mass "648.5888"
-xref: delta_composition "O(3) S Hex HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 11:09:57"
-xref: date_time_modified "2015-05-06 12:09:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_649_mono_mass "648.168383"
-xref: spec_1_neutral_loss_649_avge_mass "648.5888"
-xref: spec_1_neutral_loss_649_flag "false"
-xref: spec_1_neutral_loss_649_composition "O(3) S Hex HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_649_mono_mass "648.168383"
-xref: spec_1_neutral_loss_649_avge_mass "648.5888"
-xref: spec_1_neutral_loss_649_flag "false"
-xref: spec_1_neutral_loss_649_composition "O(3) S Hex HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1448
-name: Hex(4)
-def: "Hex(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1448]
-xref: record_id "1448"
-xref: delta_mono_mass "648.211294"
-xref: delta_avge_mass "648.5624"
-xref: delta_composition "Hex(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 11:10:47"
-xref: date_time_modified "2015-05-05 11:10:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_649_mono_mass "648.211294"
-xref: spec_1_neutral_loss_649_avge_mass "648.5624"
-xref: spec_1_neutral_loss_649_flag "false"
-xref: spec_1_neutral_loss_649_composition "Hex(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_649_mono_mass "648.211294"
-xref: spec_1_neutral_loss_649_avge_mass "648.5624"
-xref: spec_1_neutral_loss_649_flag "false"
-xref: spec_1_neutral_loss_649_composition "Hex(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1449
-name: dHex(1)Hex(2)HexNAc(2)Pent(1)
-def: "DHex Hex(2) HexNAc(2) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=2&hexnac=2&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1449]
-xref: record_id "1449"
-xref: delta_mono_mass "1008.36456"
-xref: delta_avge_mass "1008.9221"
-xref: delta_composition "dHex(1) Hex(2) HexNAc(2) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1009_mono_mass "1008.36456"
-xref: spec_1_neutral_loss_1009_avge_mass "1008.9221"
-xref: spec_1_neutral_loss_1009_flag "false"
-xref: spec_1_neutral_loss_1009_composition "dHex(1) Hex(2) HexNAc(2) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1450
-name: Hex(2)HexNAc(2)NeuAc(1)
-def: "Hex(2) HexNAc(2) NeuAc ---OR--- dHex Hex HexNAc(2) NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=2&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1450]
-xref: record_id "1450"
-xref: delta_mono_mass "1021.359809"
-xref: delta_avge_mass "1021.9208"
-xref: delta_composition "Hex(2) HexNAc(2) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-17 11:53:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1022_mono_mass "1021.359809"
-xref: spec_1_neutral_loss_1022_avge_mass "1021.9208"
-xref: spec_1_neutral_loss_1022_flag "false"
-xref: spec_1_neutral_loss_1022_composition "Hex(2) HexNAc(2) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_1022_mono_mass "1021.359809"
-xref: spec_2_neutral_loss_1022_avge_mass "1021.9208"
-xref: spec_2_neutral_loss_1022_flag "false"
-xref: spec_2_neutral_loss_1022_composition "Hex(2) HexNAc(2) NeuAc"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_1022_mono_mass "1021.359809"
-xref: spec_2_neutral_loss_1022_avge_mass "1021.9208"
-xref: spec_2_neutral_loss_1022_flag "false"
-xref: spec_2_neutral_loss_1022_composition "Hex(2) HexNAc(2) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1451
-name: Hex(3)HexNAc(2)Pent(1)
-def: "Hex(3) HexNAc(2) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=2&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1451]
-xref: record_id "1451"
-xref: delta_mono_mass "1024.359475"
-xref: delta_avge_mass "1024.9215"
-xref: delta_composition "Hex(3) HexNAc(2) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1025_mono_mass "1024.359475"
-xref: spec_1_neutral_loss_1025_avge_mass "1024.9215"
-xref: spec_1_neutral_loss_1025_flag "false"
-xref: spec_1_neutral_loss_1025_composition "Hex(3) HexNAc(2) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1452
-name: Hex(4)HexNAc(2)
-def: "Hex(4) HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1452]
-xref: record_id "1452"
-xref: delta_mono_mass "1054.370039"
-xref: delta_avge_mass "1054.9474"
-xref: delta_composition "Hex(4) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1055_mono_mass "1054.370039"
-xref: spec_1_neutral_loss_1055_avge_mass "1054.9474"
-xref: spec_1_neutral_loss_1055_flag "false"
-xref: spec_1_neutral_loss_1055_composition "Hex(4) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1453
-name: dHex(1)Hex(4)HexNAc(1)Pent(1)
-def: "DHex Hex(4) HexNAc Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=4&hexnac=1&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1453]
-xref: record_id "1453"
-xref: delta_mono_mass "1129.390834"
-xref: delta_avge_mass "1130.0107"
-xref: delta_composition "dHex(1) Hex(4) HexNAc(1) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1130_mono_mass "1129.390834"
-xref: spec_1_neutral_loss_1130_avge_mass "1130.0107"
-xref: spec_1_neutral_loss_1130_flag "false"
-xref: spec_1_neutral_loss_1130_composition "dHex(1) Hex(4) HexNAc(1) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1454
-name: dHex(1)Hex(3)HexNAc(2)Pent(1)
-def: "DHex Hex(3) HexNAc(2) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexnac=2&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1454]
-xref: record_id "1454"
-xref: delta_mono_mass "1170.417383"
-xref: delta_avge_mass "1171.0627"
-xref: delta_composition "dHex(1) Hex(3) HexNAc(2) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1171_mono_mass "1170.417383"
-xref: spec_1_neutral_loss_1171_avge_mass "1171.0627"
-xref: spec_1_neutral_loss_1171_flag "false"
-xref: spec_1_neutral_loss_1171_composition "dHex(1) Hex(3) HexNAc(2) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1455
-name: Hex(3)HexNAc(2)NeuAc(1)
-def: "Hex(3) HexNAc(2) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=2&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1455]
-xref: record_id "1455"
-xref: delta_mono_mass "1183.412632"
-xref: delta_avge_mass "1184.0614"
-xref: delta_composition "Hex(3) HexNAc(2) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1184_mono_mass "1183.412632"
-xref: spec_1_neutral_loss_1184_avge_mass "1184.0614"
-xref: spec_1_neutral_loss_1184_flag "false"
-xref: spec_1_neutral_loss_1184_composition "Hex(3) HexNAc(2) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1456
-name: Hex(4)HexNAc(2)Pent(1)
-def: "Hex(4) HexNAc(2) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexnac=2&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1456]
-xref: record_id "1456"
-xref: delta_mono_mass "1186.412298"
-xref: delta_avge_mass "1187.0621"
-xref: delta_composition "Hex(4) HexNAc(2) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1187_mono_mass "1186.412298"
-xref: spec_1_neutral_loss_1187_avge_mass "1187.0621"
-xref: spec_1_neutral_loss_1187_flag "false"
-xref: spec_1_neutral_loss_1187_composition "Hex(4) HexNAc(2) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1457
-name: Hex(3)HexNAc(3)Pent(1)
-def: "Hex(3) HexNAc(3) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=3&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1457]
-xref: record_id "1457"
-xref: delta_mono_mass "1227.438847"
-xref: delta_avge_mass "1228.114"
-xref: delta_composition "Hex(3) HexNAc(3) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1228_mono_mass "1227.438847"
-xref: spec_1_neutral_loss_1228_avge_mass "1228.114"
-xref: spec_1_neutral_loss_1228_flag "false"
-xref: spec_1_neutral_loss_1228_composition "Hex(3) HexNAc(3) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1458
-name: Hex(5)HexNAc(2)Phos(1)
-def: "Hex(5) HexNAc(2) Phos." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=1&hex=5&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1458]
-xref: record_id "1458"
-xref: delta_mono_mass "1296.389194"
-xref: delta_avge_mass "1297.0679"
-xref: delta_composition "H O(3) P Hex(5) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:43:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1297_mono_mass "1296.389194"
-xref: spec_1_neutral_loss_1297_avge_mass "1297.0679"
-xref: spec_1_neutral_loss_1297_flag "false"
-xref: spec_1_neutral_loss_1297_composition "H O(3) P Hex(5) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1459
-name: dHex(1)Hex(4)HexNAc(2)Pent(1)
-def: "DHex Hex(4) HexNAc(2) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=4&hexnac=2&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1459]
-xref: record_id "1459"
-xref: delta_mono_mass "1332.470207"
-xref: delta_avge_mass "1333.2033"
-xref: delta_composition "dHex(1) Hex(4) HexNAc(2) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1333_mono_mass "1332.470207"
-xref: spec_1_neutral_loss_1333_avge_mass "1333.2033"
-xref: spec_1_neutral_loss_1333_flag "false"
-xref: spec_1_neutral_loss_1333_composition "dHex(1) Hex(4) HexNAc(2) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1460
-name: Hex(7)HexNAc(1)
-def: "Hex(7) HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=7&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1460]
-xref: record_id "1460"
-xref: delta_mono_mass "1337.449137"
-xref: delta_avge_mass "1338.1767"
-xref: delta_composition "Hex(7) HexNAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1338_mono_mass "1337.449137"
-xref: spec_1_neutral_loss_1338_avge_mass "1338.1767"
-xref: spec_1_neutral_loss_1338_flag "false"
-xref: spec_1_neutral_loss_1338_composition "Hex(7) HexNAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1461
-name: Hex(4)HexNAc(2)NeuAc(1)
-def: "Hex(4) HexNAc(2) NeuAc ---OR--- Hex(3) HexNAc(2) dHex NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexnac=2&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1461]
-xref: record_id "1461"
-xref: delta_mono_mass "1345.465456"
-xref: delta_avge_mass "1346.202"
-xref: delta_composition "Hex(4) HexNAc(2) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-17 13:30:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1346_mono_mass "1345.465456"
-xref: spec_1_neutral_loss_1346_avge_mass "1346.202"
-xref: spec_1_neutral_loss_1346_flag "false"
-xref: spec_1_neutral_loss_1346_composition "Hex(4) HexNAc(2) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_1346_mono_mass "1345.465456"
-xref: spec_2_neutral_loss_1346_avge_mass "1346.202"
-xref: spec_2_neutral_loss_1346_flag "false"
-xref: spec_2_neutral_loss_1346_composition "Hex(4) HexNAc(2) NeuAc"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_1346_mono_mass "1345.465456"
-xref: spec_2_neutral_loss_1346_avge_mass "1346.202"
-xref: spec_2_neutral_loss_1346_flag "false"
-xref: spec_2_neutral_loss_1346_composition "Hex(4) HexNAc(2) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1462
-name: dHex(1)Hex(5)HexNAc(2)
-def: "DHex Hex(5) HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=5&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1462]
-xref: record_id "1462"
-xref: delta_mono_mass "1362.480772"
-xref: delta_avge_mass "1363.2292"
-xref: delta_composition "dHex(1) Hex(5) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1363_mono_mass "1362.480772"
-xref: spec_1_neutral_loss_1363_avge_mass "1363.2292"
-xref: spec_1_neutral_loss_1363_flag "false"
-xref: spec_1_neutral_loss_1363_composition "dHex(1) Hex(5) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1463
-name: dHex(1)Hex(3)HexNAc(3)Pent(1)
-def: "DHex Hex(3) HexNAc(3) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexnac=3&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1463]
-xref: record_id "1463"
-xref: delta_mono_mass "1373.496756"
-xref: delta_avge_mass "1374.2552"
-xref: delta_composition "dHex(1) Hex(3) HexNAc(3) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1374_mono_mass "1373.496756"
-xref: spec_1_neutral_loss_1374_avge_mass "1374.2552"
-xref: spec_1_neutral_loss_1374_flag "false"
-xref: spec_1_neutral_loss_1374_composition "dHex(1) Hex(3) HexNAc(3) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1464
-name: Hex(3)HexNAc(4)Sulf(1)
-def: "Hex(3) HexNAc(4) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=3&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1464]
-xref: record_id "1464"
-xref: delta_mono_mass "1378.432776"
-xref: delta_avge_mass "1379.2551"
-xref: delta_composition "O(3) S Hex(3) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:33:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1379_mono_mass "1378.432776"
-xref: spec_1_neutral_loss_1379_avge_mass "1379.2551"
-xref: spec_1_neutral_loss_1379_flag "false"
-xref: spec_1_neutral_loss_1379_composition "O(3) S Hex(3) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1465
-name: Hex(6)HexNAc(2)
-def: "M6/Man6." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=6&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1465]
-xref: record_id "1465"
-xref: delta_mono_mass "1378.475686"
-xref: delta_avge_mass "1379.2286"
-xref: delta_composition "Hex(6) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2020-08-02 11:49:46"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1379_mono_mass "1378.475686"
-xref: spec_1_neutral_loss_1379_avge_mass "1379.2286"
-xref: spec_1_neutral_loss_1379_flag "false"
-xref: spec_1_neutral_loss_1379_composition "Hex(6) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1466
-name: Hex(4)HexNAc(3)Pent(1)
-def: "Hex(4) HexNAc(3) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexnac=3&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1466]
-xref: record_id "1466"
-xref: delta_mono_mass "1389.491671"
-xref: delta_avge_mass "1390.2546"
-xref: delta_composition "Hex(4) HexNAc(3) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1390_mono_mass "1389.491671"
-xref: spec_1_neutral_loss_1390_avge_mass "1390.2546"
-xref: spec_1_neutral_loss_1390_flag "false"
-xref: spec_1_neutral_loss_1390_composition "Hex(4) HexNAc(3) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1467
-name: dHex(1)Hex(4)HexNAc(3)
-def: "DHex Hex(4) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=4&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1467]
-xref: record_id "1467"
-xref: delta_mono_mass "1403.507321"
-xref: delta_avge_mass "1404.2812"
-xref: delta_composition "dHex(1) Hex(4) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1404_mono_mass "1403.507321"
-xref: spec_1_neutral_loss_1404_avge_mass "1404.2812"
-xref: spec_1_neutral_loss_1404_flag "false"
-xref: spec_1_neutral_loss_1404_composition "dHex(1) Hex(4) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1468
-name: Hex(5)HexNAc(3)
-def: "Hex(5) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=5&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1468]
-xref: record_id "1468"
-xref: delta_mono_mass "1419.502235"
-xref: delta_avge_mass "1420.2806"
-xref: delta_composition "Hex(5) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1420_mono_mass "1419.502235"
-xref: spec_1_neutral_loss_1420_avge_mass "1420.2806"
-xref: spec_1_neutral_loss_1420_flag "false"
-xref: spec_1_neutral_loss_1420_composition "Hex(5) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1469
-name: Hex(3)HexNAc(4)Pent(1)
-def: "Hex(3) HexNAc(4) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=4&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1469]
-xref: record_id "1469"
-xref: delta_mono_mass "1430.51822"
-xref: delta_avge_mass "1431.3065"
-xref: delta_composition "Hex(3) HexNAc(4) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1431_mono_mass "1430.51822"
-xref: spec_1_neutral_loss_1431_avge_mass "1431.3065"
-xref: spec_1_neutral_loss_1431_flag "false"
-xref: spec_1_neutral_loss_1431_composition "Hex(3) HexNAc(4) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1470
-name: Hex(6)HexNAc(2)Phos(1)
-def: "Hex(6) HexNAc(2) Phos." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=1&hex=6&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1470]
-xref: record_id "1470"
-xref: delta_mono_mass "1458.442017"
-xref: delta_avge_mass "1459.2085"
-xref: delta_composition "H O(3) P Hex(6) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:43:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1459_mono_mass "1458.442017"
-xref: spec_1_neutral_loss_1459_avge_mass "1459.2085"
-xref: spec_1_neutral_loss_1459_flag "false"
-xref: spec_1_neutral_loss_1459_composition "H O(3) P Hex(6) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1471
-name: dHex(1)Hex(4)HexNAc(3)Sulf(1)
-def: "DHex Hex(4) HexNAc(3) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=4&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1471]
-xref: record_id "1471"
-xref: delta_mono_mass "1483.464135"
-xref: delta_avge_mass "1484.3444"
-xref: delta_composition "O(3) S dHex Hex(4) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:34:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1484_mono_mass "1483.464135"
-xref: spec_1_neutral_loss_1484_avge_mass "1484.3444"
-xref: spec_1_neutral_loss_1484_flag "false"
-xref: spec_1_neutral_loss_1484_composition "O(3) S dHex Hex(4) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1472
-name: dHex(1)Hex(5)HexNAc(2)Pent(1)
-def: "DHex Hex(5) HexNAc(2) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=5&hexnac=2&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1472]
-xref: record_id "1472"
-xref: delta_mono_mass "1494.52303"
-xref: delta_avge_mass "1495.3439"
-xref: delta_composition "dHex(1) Hex(5) HexNAc(2) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1495_mono_mass "1494.52303"
-xref: spec_1_neutral_loss_1495_avge_mass "1495.3439"
-xref: spec_1_neutral_loss_1495_flag "false"
-xref: spec_1_neutral_loss_1495_composition "dHex(1) Hex(5) HexNAc(2) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1473
-name: Hex(8)HexNAc(1)
-def: "Hex(8) HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=8&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1473]
-xref: record_id "1473"
-xref: delta_mono_mass "1499.501961"
-xref: delta_avge_mass "1500.3173"
-xref: delta_composition "Hex(8) HexNAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1500_mono_mass "1499.501961"
-xref: spec_1_neutral_loss_1500_avge_mass "1500.3173"
-xref: spec_1_neutral_loss_1500_flag "false"
-xref: spec_1_neutral_loss_1500_composition "Hex(8) HexNAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1474
-name: dHex(1)Hex(3)HexNAc(3)Pent(2)
-def: "DHex Hex(3) HexNAc(3) Pent(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexnac=3&pent=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1474]
-xref: record_id "1474"
-xref: delta_mono_mass "1505.539015"
-xref: delta_avge_mass "1506.3698"
-xref: delta_composition "dHex(1) Hex(3) HexNAc(3) Pent(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1506_mono_mass "1505.539015"
-xref: spec_1_neutral_loss_1506_avge_mass "1506.3698"
-xref: spec_1_neutral_loss_1506_flag "false"
-xref: spec_1_neutral_loss_1506_composition "dHex(1) Hex(3) HexNAc(3) Pent(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1475
-name: dHex(2)Hex(3)HexNAc(3)Pent(1)
-def: "DHex(2) Hex(3) HexNAc(3) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=3&hexnac=3&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1475]
-xref: record_id "1475"
-xref: delta_mono_mass "1519.554665"
-xref: delta_avge_mass "1520.3964"
-xref: delta_composition "dHex(2) Hex(3) HexNAc(3) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1520_mono_mass "1519.554665"
-xref: spec_1_neutral_loss_1520_avge_mass "1520.3964"
-xref: spec_1_neutral_loss_1520_flag "false"
-xref: spec_1_neutral_loss_1520_composition "dHex(2) Hex(3) HexNAc(3) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1476
-name: dHex(1)Hex(3)HexNAc(4)Sulf(1)
-def: "DHex Hex(3) HexNAc(4) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=3&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1476]
-xref: record_id "1476"
-xref: delta_mono_mass "1524.490684"
-xref: delta_avge_mass "1525.3963"
-xref: delta_composition "O(3) S dHex Hex(3) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:34:38"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1525_mono_mass "1524.490684"
-xref: spec_1_neutral_loss_1525_avge_mass "1525.3963"
-xref: spec_1_neutral_loss_1525_flag "false"
-xref: spec_1_neutral_loss_1525_composition "O(3) S dHex Hex(3) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1477
-name: dHex(1)Hex(6)HexNAc(2)
-def: "DHex Hex(6) HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=6&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1477]
-xref: record_id "1477"
-xref: delta_mono_mass "1524.533595"
-xref: delta_avge_mass "1525.3698"
-xref: delta_composition "dHex(1) Hex(6) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1525_mono_mass "1524.533595"
-xref: spec_1_neutral_loss_1525_avge_mass "1525.3698"
-xref: spec_1_neutral_loss_1525_flag "false"
-xref: spec_1_neutral_loss_1525_composition "dHex(1) Hex(6) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1478
-name: dHex(1)Hex(4)HexNAc(3)Pent(1)
-def: "DHex Hex(4) HexNAc(3) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=4&hexnac=3&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1478]
-xref: record_id "1478"
-xref: delta_mono_mass "1535.549579"
-xref: delta_avge_mass "1536.3958"
-xref: delta_composition "dHex(1) Hex(4) HexNAc(3) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1536_mono_mass "1535.549579"
-xref: spec_1_neutral_loss_1536_avge_mass "1536.3958"
-xref: spec_1_neutral_loss_1536_flag "false"
-xref: spec_1_neutral_loss_1536_composition "dHex(1) Hex(4) HexNAc(3) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1479
-name: Hex(4)HexNAc(4)Sulf(1)
-def: "Hex(4) HexNAc(4) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=4&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1479]
-xref: record_id "1479"
-xref: delta_mono_mass "1540.485599"
-xref: delta_avge_mass "1541.3957"
-xref: delta_composition "O(3) S Hex(4) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:34:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1541_mono_mass "1540.485599"
-xref: spec_1_neutral_loss_1541_avge_mass "1541.3957"
-xref: spec_1_neutral_loss_1541_flag "false"
-xref: spec_1_neutral_loss_1541_composition "O(3) S Hex(4) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1480
-name: Hex(7)HexNAc(2)
-def: "M7/Man7." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=7&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1480]
-xref: record_id "1480"
-xref: delta_mono_mass "1540.52851"
-xref: delta_avge_mass "1541.3692"
-xref: delta_composition "Hex(7) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2020-08-02 11:49:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1541_mono_mass "1540.52851"
-xref: spec_1_neutral_loss_1541_avge_mass "1541.3692"
-xref: spec_1_neutral_loss_1541_flag "false"
-xref: spec_1_neutral_loss_1541_composition "Hex(7) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1481
-name: dHex(2)Hex(4)HexNAc(3)
-def: "DHex(2) Hex(4) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=4&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1481]
-xref: record_id "1481"
-xref: delta_mono_mass "1549.56523"
-xref: delta_avge_mass "1550.4224"
-xref: delta_composition "dHex(2) Hex(4) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1550_mono_mass "1549.56523"
-xref: spec_1_neutral_loss_1550_avge_mass "1550.4224"
-xref: spec_1_neutral_loss_1550_flag "false"
-xref: spec_1_neutral_loss_1550_composition "dHex(2) Hex(4) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1482
-name: Hex(5)HexNAc(3)Pent(1)
-def: "Hex(5) HexNAc(3) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=5&hexnac=3&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1482]
-xref: record_id "1482"
-xref: delta_mono_mass "1551.544494"
-xref: delta_avge_mass "1552.3952"
-xref: delta_composition "Hex(5) HexNAc(3) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1552_mono_mass "1551.544494"
-xref: spec_1_neutral_loss_1552_avge_mass "1552.3952"
-xref: spec_1_neutral_loss_1552_flag "false"
-xref: spec_1_neutral_loss_1552_composition "Hex(5) HexNAc(3) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1483
-name: Hex(4)HexNAc(3)NeuGc(1)
-def: "Hex(4) HexNAc(3) NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexnac=3&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1483]
-xref: record_id "1483"
-xref: delta_mono_mass "1564.539743"
-xref: delta_avge_mass "1565.3939"
-xref: delta_composition "Hex(4) HexNAc(3) NeuGc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1565_mono_mass "1564.539743"
-xref: spec_1_neutral_loss_1565_avge_mass "1565.3939"
-xref: spec_1_neutral_loss_1565_flag "false"
-xref: spec_1_neutral_loss_1565_composition "Hex(4) HexNAc(3) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1484
-name: dHex(1)Hex(5)HexNAc(3)
-def: "DHex Hex(5) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=5&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1484]
-xref: record_id "1484"
-xref: delta_mono_mass "1565.560144"
-xref: delta_avge_mass "1566.4218"
-xref: delta_composition "dHex(1) Hex(5) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1566_mono_mass "1565.560144"
-xref: spec_1_neutral_loss_1566_avge_mass "1566.4218"
-xref: spec_1_neutral_loss_1566_flag "false"
-xref: spec_1_neutral_loss_1566_composition "dHex(1) Hex(5) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1485
-name: dHex(1)Hex(3)HexNAc(4)Pent(1)
-def: "DHex Hex(3) HexNAc(4) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexnac=4&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1485]
-xref: record_id "1485"
-xref: delta_mono_mass "1576.576129"
-xref: delta_avge_mass "1577.4477"
-xref: delta_composition "dHex(1) Hex(3) HexNAc(4) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1577_mono_mass "1576.576129"
-xref: spec_1_neutral_loss_1577_avge_mass "1577.4477"
-xref: spec_1_neutral_loss_1577_flag "false"
-xref: spec_1_neutral_loss_1577_composition "dHex(1) Hex(3) HexNAc(4) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1486
-name: Hex(3)HexNAc(5)Sulf(1)
-def: "Hex(3) HexNAc(5) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=3&hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1486]
-xref: record_id "1486"
-xref: delta_mono_mass "1581.512148"
-xref: delta_avge_mass "1582.4476"
-xref: delta_composition "O(3) S Hex(3) HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:35:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1582_mono_mass "1581.512148"
-xref: spec_1_neutral_loss_1582_avge_mass "1582.4476"
-xref: spec_1_neutral_loss_1582_flag "false"
-xref: spec_1_neutral_loss_1582_composition "O(3) S Hex(3) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1487
-name: Hex(6)HexNAc(3)
-def: "Hex(6) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=6&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1487]
-xref: record_id "1487"
-xref: delta_mono_mass "1581.555059"
-xref: delta_avge_mass "1582.4212"
-xref: delta_composition "Hex(6) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1582_mono_mass "1581.555059"
-xref: spec_1_neutral_loss_1582_avge_mass "1582.4212"
-xref: spec_1_neutral_loss_1582_flag "false"
-xref: spec_1_neutral_loss_1582_composition "Hex(6) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1488
-name: Hex(3)HexNAc(4)NeuAc(1)
-def: "Hex(3) HexNAc(4) NeuAc ---OR--- Hex(2) HexNAc(4) dHex NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=4&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1488]
-xref: record_id "1488"
-xref: delta_mono_mass "1589.571378"
-xref: delta_avge_mass "1590.4465"
-xref: delta_composition "Hex(3) HexNAc(4) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-17 16:47:58"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1590_mono_mass "1589.571378"
-xref: spec_1_neutral_loss_1590_avge_mass "1590.4465"
-xref: spec_1_neutral_loss_1590_flag "false"
-xref: spec_1_neutral_loss_1590_composition "Hex(3) HexNAc(4) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1489
-name: Hex(4)HexNAc(4)Pent(1)
-def: "Hex(4) HexNAc(4) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexnac=4&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1489]
-xref: record_id "1489"
-xref: delta_mono_mass "1592.571043"
-xref: delta_avge_mass "1593.4471"
-xref: delta_composition "Hex(4) HexNAc(4) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1593_mono_mass "1592.571043"
-xref: spec_1_neutral_loss_1593_avge_mass "1593.4471"
-xref: spec_1_neutral_loss_1593_flag "false"
-xref: spec_1_neutral_loss_1593_composition "Hex(4) HexNAc(4) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1490
-name: Hex(7)HexNAc(2)Phos(1)
-def: "Hex(7) HexNAc(2) Phos." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=1&hex=7&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1490]
-xref: record_id "1490"
-xref: delta_mono_mass "1620.494841"
-xref: delta_avge_mass "1621.3491"
-xref: delta_composition "H O(3) P Hex(7) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:43:48"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1621_mono_mass "1620.494841"
-xref: spec_1_neutral_loss_1621_avge_mass "1621.3491"
-xref: spec_1_neutral_loss_1621_flag "false"
-xref: spec_1_neutral_loss_1621_composition "H O(3) P Hex(7) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1491
-name: Hex(4)HexNAc(4)Me(2)Pent(1)
-def: "Hex(4) HexNAc(4) Me(2) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexnac=4&methyl=2&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1491]
-xref: record_id "1491"
-xref: delta_mono_mass "1620.602343"
-xref: delta_avge_mass "1621.5003"
-xref: delta_composition "Hex(4) HexNAc(4) Me(2) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1621_mono_mass "1620.602343"
-xref: spec_1_neutral_loss_1621_avge_mass "1621.5003"
-xref: spec_1_neutral_loss_1621_flag "false"
-xref: spec_1_neutral_loss_1621_composition "Hex(4) HexNAc(4) Me(2) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1492
-name: dHex(1)Hex(3)HexNAc(3)Pent(3)
-def: "DHex Hex(3) HexNAc(3) Pent(3) ---OR--- Hex(4) HexNAc(2) dHex(2) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?pent=3&dhex=1&hex=3&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1492]
-xref: record_id "1492"
-xref: delta_mono_mass "1637.581274"
-xref: delta_avge_mass "1638.4844"
-xref: delta_composition "Pent(3) dHex Hex(3) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-22 10:46:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1638_mono_mass "1637.581274"
-xref: spec_1_neutral_loss_1638_avge_mass "1638.4844"
-xref: spec_1_neutral_loss_1638_flag "false"
-xref: spec_1_neutral_loss_1638_composition "Pent(3) dHex Hex(3) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1493
-name: dHex(1)Hex(5)HexNAc(3)Sulf(1)
-def: "DHex Hex(5) HexNAc(3) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=5&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1493]
-xref: record_id "1493"
-xref: delta_mono_mass "1645.516959"
-xref: delta_avge_mass "1646.485"
-xref: delta_composition "O(3) S dHex Hex(5) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:35:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1646_mono_mass "1645.516959"
-xref: spec_1_neutral_loss_1646_avge_mass "1646.485"
-xref: spec_1_neutral_loss_1646_flag "false"
-xref: spec_1_neutral_loss_1646_composition "O(3) S dHex Hex(5) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1494
-name: dHex(2)Hex(3)HexNAc(3)Pent(2)
-def: "DHex(2) Hex(3) HexNAc(3) Pent(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=3&hexnac=3&pent=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1494]
-xref: record_id "1494"
-xref: delta_mono_mass "1651.596924"
-xref: delta_avge_mass "1652.511"
-xref: delta_composition "dHex(2) Hex(3) HexNAc(3) Pent(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1652_mono_mass "1651.596924"
-xref: spec_1_neutral_loss_1652_avge_mass "1652.511"
-xref: spec_1_neutral_loss_1652_flag "false"
-xref: spec_1_neutral_loss_1652_composition "dHex(2) Hex(3) HexNAc(3) Pent(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1495
-name: Hex(6)HexNAc(3)Phos(1)
-def: "Hex(6) HexNAc(3) Phos." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=1&hex=6&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1495]
-xref: record_id "1495"
-xref: delta_mono_mass "1661.52139"
-xref: delta_avge_mass "1662.4011"
-xref: delta_composition "H O(3) P Hex(6) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:43:58"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1662_mono_mass "1661.52139"
-xref: spec_1_neutral_loss_1662_avge_mass "1662.4011"
-xref: spec_1_neutral_loss_1662_flag "false"
-xref: spec_1_neutral_loss_1662_composition "H O(3) P Hex(6) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1496
-name: Hex(4)HexNAc(5)
-def: "Hex(4) HexNAc(5)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1496]
-xref: record_id "1496"
-xref: delta_mono_mass "1663.608157"
-xref: delta_avge_mass "1664.525"
-xref: delta_composition "Hex(4) HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1664_mono_mass "1663.608157"
-xref: spec_1_neutral_loss_1664_avge_mass "1664.525"
-xref: spec_1_neutral_loss_1664_flag "false"
-xref: spec_1_neutral_loss_1664_composition "Hex(4) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1497
-name: dHex(3)Hex(3)HexNAc(3)Pent(1)
-def: "DHex(3) Hex(3) HexNAc(3) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=3&hex=3&hexnac=3&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1497]
-xref: record_id "1497"
-xref: delta_mono_mass "1665.612574"
-xref: delta_avge_mass "1666.5376"
-xref: delta_composition "dHex(3) Hex(3) HexNAc(3) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1666_mono_mass "1665.612574"
-xref: spec_1_neutral_loss_1666_avge_mass "1666.5376"
-xref: spec_1_neutral_loss_1666_flag "false"
-xref: spec_1_neutral_loss_1666_composition "dHex(3) Hex(3) HexNAc(3) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1498
-name: dHex(2)Hex(4)HexNAc(3)Pent(1)
-def: "DHex(2) Hex(4) HexNAc(3) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=4&hexnac=3&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1498]
-xref: record_id "1498"
-xref: delta_mono_mass "1681.607488"
-xref: delta_avge_mass "1682.537"
-xref: delta_composition "dHex(2) Hex(4) HexNAc(3) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1682_mono_mass "1681.607488"
-xref: spec_1_neutral_loss_1682_avge_mass "1682.537"
-xref: spec_1_neutral_loss_1682_flag "false"
-xref: spec_1_neutral_loss_1682_composition "dHex(2) Hex(4) HexNAc(3) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1499
-name: dHex(1)Hex(4)HexNAc(4)Sulf(1)
-def: "DHex Hex(4) HexNAc(4) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=4&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1499]
-xref: record_id "1499"
-xref: delta_mono_mass "1686.543508"
-xref: delta_avge_mass "1687.5369"
-xref: delta_composition "O(3) S dHex Hex(4) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:35:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1687_mono_mass "1686.543508"
-xref: spec_1_neutral_loss_1687_avge_mass "1687.5369"
-xref: spec_1_neutral_loss_1687_flag "false"
-xref: spec_1_neutral_loss_1687_composition "O(3) S dHex Hex(4) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1500
-name: dHex(1)Hex(7)HexNAc(2)
-def: "DHex Hex(7) HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=7&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1500]
-xref: record_id "1500"
-xref: delta_mono_mass "1686.586419"
-xref: delta_avge_mass "1687.5104"
-xref: delta_composition "dHex(1) Hex(7) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1687_mono_mass "1686.586419"
-xref: spec_1_neutral_loss_1687_avge_mass "1687.5104"
-xref: spec_1_neutral_loss_1687_flag "false"
-xref: spec_1_neutral_loss_1687_composition "dHex(1) Hex(7) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1501
-name: dHex(1)Hex(4)HexNAc(3)NeuAc(1)
-def: "DHex Hex(4) HexNAc(3) NeuAc ---OR--- dHex(2) Hex(3) HexNAc(3) NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=4&hexnac=3&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1501]
-xref: record_id "1501"
-xref: delta_mono_mass "1694.602737"
-xref: delta_avge_mass "1695.5357"
-xref: delta_composition "dHex Hex(4) HexNAc(3) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-22 10:54:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1695_mono_mass "1694.602737"
-xref: spec_1_neutral_loss_1695_avge_mass "1695.5357"
-xref: spec_1_neutral_loss_1695_flag "false"
-xref: spec_1_neutral_loss_1695_composition "dHex Hex(4) HexNAc(3) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_1695_mono_mass "1694.602737"
-xref: spec_2_neutral_loss_1695_avge_mass "1695.5357"
-xref: spec_2_neutral_loss_1695_flag "false"
-xref: spec_2_neutral_loss_1695_composition "dHex Hex(4) HexNAc(3) NeuAc"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_1695_mono_mass "1694.602737"
-xref: spec_2_neutral_loss_1695_avge_mass "1695.5357"
-xref: spec_2_neutral_loss_1695_flag "false"
-xref: spec_2_neutral_loss_1695_composition "dHex Hex(4) HexNAc(3) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1502
-name: Hex(7)HexNAc(2)Phos(2)
-def: "Hex(7) HexNAc(2) Phos(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=2&hex=7&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1502]
-xref: record_id "1502"
-xref: delta_mono_mass "1700.461172"
-xref: delta_avge_mass "1701.329"
-xref: delta_composition "H(2) O(6) P(2) Hex(7) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:44:09"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1701_mono_mass "1700.461172"
-xref: spec_1_neutral_loss_1701_avge_mass "1701.329"
-xref: spec_1_neutral_loss_1701_flag "false"
-xref: spec_1_neutral_loss_1701_composition "H(2) O(6) P(2) Hex(7) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1503
-name: Hex(5)HexNAc(4)Sulf(1)
-def: "Hex(5) HexNAc(4) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=5&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1503]
-xref: record_id "1503"
-xref: delta_mono_mass "1702.538423"
-xref: delta_avge_mass "1703.5363"
-xref: delta_composition "O(3) S Hex(5) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:35:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1703_mono_mass "1702.538423"
-xref: spec_1_neutral_loss_1703_avge_mass "1703.5363"
-xref: spec_1_neutral_loss_1703_flag "false"
-xref: spec_1_neutral_loss_1703_composition "O(3) S Hex(5) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1504
-name: Hex(8)HexNAc(2)
-def: "M8/Man8." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=8&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1504]
-xref: record_id "1504"
-xref: delta_mono_mass "1702.581333"
-xref: delta_avge_mass "1703.5098"
-xref: delta_composition "Hex(8) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2020-08-02 11:49:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1703_mono_mass "1702.581333"
-xref: spec_1_neutral_loss_1703_avge_mass "1703.5098"
-xref: spec_1_neutral_loss_1703_flag "false"
-xref: spec_1_neutral_loss_1703_composition "Hex(8) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1505
-name: dHex(1)Hex(3)HexNAc(4)Pent(2)
-def: "DHex Hex(3) HexNAc(4) Pent(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexnac=4&pent=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1505]
-xref: record_id "1505"
-xref: delta_mono_mass "1708.618387"
-xref: delta_avge_mass "1709.5623"
-xref: delta_composition "dHex(1) Hex(3) HexNAc(4) Pent(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1709_mono_mass "1708.618387"
-xref: spec_1_neutral_loss_1709_avge_mass "1709.5623"
-xref: spec_1_neutral_loss_1709_flag "false"
-xref: spec_1_neutral_loss_1709_composition "dHex(1) Hex(3) HexNAc(4) Pent(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1506
-name: dHex(1)Hex(4)HexNAc(3)NeuGc(1)
-def: "DHex Hex(4) HexNAc(3) NeuGc ---OR--- Hex(5) HexNAc(3) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=4&hexnac=3&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1506]
-xref: record_id "1506"
-xref: delta_mono_mass "1710.597652"
-xref: delta_avge_mass "1711.5351"
-xref: delta_composition "dHex Hex(4) HexNAc(3) NeuGc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-22 11:04:22"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1711_mono_mass "1710.597652"
-xref: spec_1_neutral_loss_1711_avge_mass "1711.5351"
-xref: spec_1_neutral_loss_1711_flag "false"
-xref: spec_1_neutral_loss_1711_composition "dHex Hex(4) HexNAc(3) NeuGc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1507
-name: dHex(2)Hex(3)HexNAc(4)Pent(1)
-def: "DHex(2) Hex(3) HexNAc(4) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=3&hexnac=4&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1507]
-xref: record_id "1507"
-xref: delta_mono_mass "1722.634037"
-xref: delta_avge_mass "1723.5889"
-xref: delta_composition "dHex(2) Hex(3) HexNAc(4) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1723_mono_mass "1722.634037"
-xref: spec_1_neutral_loss_1723_avge_mass "1723.5889"
-xref: spec_1_neutral_loss_1723_flag "false"
-xref: spec_1_neutral_loss_1723_composition "dHex(2) Hex(3) HexNAc(4) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1508
-name: dHex(1)Hex(3)HexNAc(5)Sulf(1)
-def: "DHex Hex(3) HexNAc(5) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=3&hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1508]
-xref: record_id "1508"
-xref: delta_mono_mass "1727.570057"
-xref: delta_avge_mass "1728.5888"
-xref: delta_composition "O(3) S dHex Hex(3) HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:36:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1728_mono_mass "1727.570057"
-xref: spec_1_neutral_loss_1728_avge_mass "1728.5888"
-xref: spec_1_neutral_loss_1728_flag "false"
-xref: spec_1_neutral_loss_1728_composition "O(3) S dHex Hex(3) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1509
-name: dHex(1)Hex(6)HexNAc(3)
-def: "DHex Hex(6) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=6&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1509]
-xref: record_id "1509"
-xref: delta_mono_mass "1727.612968"
-xref: delta_avge_mass "1728.5624"
-xref: delta_composition "dHex(1) Hex(6) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1728_mono_mass "1727.612968"
-xref: spec_1_neutral_loss_1728_avge_mass "1728.5624"
-xref: spec_1_neutral_loss_1728_flag "false"
-xref: spec_1_neutral_loss_1728_composition "dHex(1) Hex(6) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1510
-name: dHex(1)Hex(3)HexNAc(4)NeuAc(1)
-def: "DHex Hex(3) HexNAc(4) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexnac=4&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1510]
-xref: record_id "1510"
-xref: delta_mono_mass "1735.629286"
-xref: delta_avge_mass "1736.5877"
-xref: delta_composition "dHex(1) Hex(3) HexNAc(4) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1736_mono_mass "1735.629286"
-xref: spec_1_neutral_loss_1736_avge_mass "1736.5877"
-xref: spec_1_neutral_loss_1736_flag "false"
-xref: spec_1_neutral_loss_1736_composition "dHex(1) Hex(3) HexNAc(4) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1511
-name: dHex(3)Hex(3)HexNAc(4)
-def: "DHex(3) Hex(3) HexNAc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=3&hex=3&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1511]
-xref: record_id "1511"
-xref: delta_mono_mass "1736.649688"
-xref: delta_avge_mass "1737.6155"
-xref: delta_composition "dHex(3) Hex(3) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1737_mono_mass "1736.649688"
-xref: spec_1_neutral_loss_1737_avge_mass "1737.6155"
-xref: spec_1_neutral_loss_1737_flag "false"
-xref: spec_1_neutral_loss_1737_composition "dHex(3) Hex(3) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1512
-name: dHex(1)Hex(4)HexNAc(4)Pent(1)
-def: "DHex Hex(4) HexNAc(4) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=4&hexnac=4&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1512]
-xref: record_id "1512"
-xref: delta_mono_mass "1738.628952"
-xref: delta_avge_mass "1739.5883"
-xref: delta_composition "dHex(1) Hex(4) HexNAc(4) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1739_mono_mass "1738.628952"
-xref: spec_1_neutral_loss_1739_avge_mass "1739.5883"
-xref: spec_1_neutral_loss_1739_flag "false"
-xref: spec_1_neutral_loss_1739_composition "dHex(1) Hex(4) HexNAc(4) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1513
-name: Hex(4)HexNAc(5)Sulf(1)
-def: "Hex(4) HexNAc(5) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=4&hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1513]
-xref: record_id "1513"
-xref: delta_mono_mass "1743.564972"
-xref: delta_avge_mass "1744.5882"
-xref: delta_composition "O(3) S Hex(4) HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:36:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1744_mono_mass "1743.564972"
-xref: spec_1_neutral_loss_1744_avge_mass "1744.5882"
-xref: spec_1_neutral_loss_1744_flag "false"
-xref: spec_1_neutral_loss_1744_composition "O(3) S Hex(4) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1514
-name: Hex(7)HexNAc(3)
-def: "Hex(7) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=7&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1514]
-xref: record_id "1514"
-xref: delta_mono_mass "1743.607882"
-xref: delta_avge_mass "1744.5618"
-xref: delta_composition "Hex(7) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1744_mono_mass "1743.607882"
-xref: spec_1_neutral_loss_1744_avge_mass "1744.5618"
-xref: spec_1_neutral_loss_1744_flag "false"
-xref: spec_1_neutral_loss_1744_composition "Hex(7) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1515
-name: dHex(1)Hex(4)HexNAc(3)NeuAc(1)Sulf(1)
-def: "DHex Hex(4) HexNAc(3) NeuAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=4&hexnac=3&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1515]
-xref: record_id "1515"
-xref: delta_mono_mass "1774.559552"
-xref: delta_avge_mass "1775.5989"
-xref: delta_composition "O(3) S dHex Hex(4) HexNAc(3) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:36:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1775_mono_mass "1774.559552"
-xref: spec_1_neutral_loss_1775_avge_mass "1775.5989"
-xref: spec_1_neutral_loss_1775_flag "false"
-xref: spec_1_neutral_loss_1775_composition "O(3) S dHex Hex(4) HexNAc(3) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1516
-name: Hex(5)HexNAc(4)Me(2)Pent(1)
-def: "Hex(5) HexNAc(4) Me(2) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=5&hexnac=4&methyl=2&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1516]
-xref: record_id "1516"
-xref: delta_mono_mass "1782.655167"
-xref: delta_avge_mass "1783.6409"
-xref: delta_composition "Hex(5) HexNAc(4) Me(2) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1783_mono_mass "1782.655167"
-xref: spec_1_neutral_loss_1783_avge_mass "1783.6409"
-xref: spec_1_neutral_loss_1783_flag "false"
-xref: spec_1_neutral_loss_1783_composition "Hex(5) HexNAc(4) Me(2) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1517
-name: Hex(3)HexNAc(6)Sulf(1)
-def: "Hex(3) HexNAc(6) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=3&hexnac=6&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1517]
-xref: record_id "1517"
-xref: delta_mono_mass "1784.591521"
-xref: delta_avge_mass "1785.6401"
-xref: delta_composition "O(3) S Hex(3) HexNAc(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:36:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1785_mono_mass "1784.591521"
-xref: spec_1_neutral_loss_1785_avge_mass "1785.6401"
-xref: spec_1_neutral_loss_1785_flag "false"
-xref: spec_1_neutral_loss_1785_composition "O(3) S Hex(3) HexNAc(6)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1518
-name: dHex(1)Hex(6)HexNAc(3)Sulf(1)
-def: "DHex Hex(6) HexNAc(3) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=6&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1518]
-xref: record_id "1518"
-xref: delta_mono_mass "1807.569782"
-xref: delta_avge_mass "1808.6256"
-xref: delta_composition "O(3) S dHex Hex(6) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:36:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1808_mono_mass "1807.569782"
-xref: spec_1_neutral_loss_1808_avge_mass "1808.6256"
-xref: spec_1_neutral_loss_1808_flag "false"
-xref: spec_1_neutral_loss_1808_composition "O(3) S dHex Hex(6) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1519
-name: dHex(1)Hex(4)HexNAc(5)
-def: "DHex Hex(4) HexNAc(5)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=4&hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1519]
-xref: record_id "1519"
-xref: delta_mono_mass "1809.666066"
-xref: delta_avge_mass "1810.6662"
-xref: delta_composition "dHex(1) Hex(4) HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1810_mono_mass "1809.666066"
-xref: spec_1_neutral_loss_1810_avge_mass "1810.6662"
-xref: spec_1_neutral_loss_1810_flag "false"
-xref: spec_1_neutral_loss_1810_composition "dHex(1) Hex(4) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1520
-name: dHex(1)Hex(5)HexA(1)HexNAc(3)Sulf(1)
-def: "DHex Hex(5) HexA HexNAc(3) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=5&hexa=1&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1520]
-xref: record_id "1520"
-xref: delta_mono_mass "1821.549047"
-xref: delta_avge_mass "1822.6091"
-xref: delta_composition "O(3) S dHex Hex(5) HexA HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:37:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1822_mono_mass "1821.549047"
-xref: spec_1_neutral_loss_1822_avge_mass "1822.6091"
-xref: spec_1_neutral_loss_1822_flag "false"
-xref: spec_1_neutral_loss_1822_composition "O(3) S dHex Hex(5) HexA HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1521
-name: Hex(7)HexNAc(3)Phos(1)
-def: "Hex(7) HexNAc(3) Phos." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=1&hex=7&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1521]
-xref: record_id "1521"
-xref: delta_mono_mass "1823.574213"
-xref: delta_avge_mass "1824.5417"
-xref: delta_composition "H O(3) P Hex(7) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:44:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1824_mono_mass "1823.574213"
-xref: spec_1_neutral_loss_1824_avge_mass "1824.5417"
-xref: spec_1_neutral_loss_1824_flag "false"
-xref: spec_1_neutral_loss_1824_composition "H O(3) P Hex(7) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1522
-name: Hex(6)HexNAc(4)Me(3)
-def: "Hex(6) HexNAc(4) Me(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=6&hexnac=4&methyl=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1522]
-xref: record_id "1522"
-xref: delta_mono_mass "1826.681382"
-xref: delta_avge_mass "1827.6934"
-xref: delta_composition "Hex(6) HexNAc(4) Me(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1827_mono_mass "1826.681382"
-xref: spec_1_neutral_loss_1827_avge_mass "1827.6934"
-xref: spec_1_neutral_loss_1827_flag "false"
-xref: spec_1_neutral_loss_1827_composition "Hex(6) HexNAc(4) Me(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1523
-name: dHex(2)Hex(4)HexNAc(4)Sulf(1)
-def: "DHex(2) Hex(4) HexNAc(4) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=2&hex=4&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1523]
-xref: record_id "1523"
-xref: delta_mono_mass "1832.601417"
-xref: delta_avge_mass "1833.6781"
-xref: delta_composition "O(3) S dHex(2) Hex(4) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:37:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1833_mono_mass "1832.601417"
-xref: spec_1_neutral_loss_1833_avge_mass "1833.6781"
-xref: spec_1_neutral_loss_1833_flag "false"
-xref: spec_1_neutral_loss_1833_composition "O(3) S dHex(2) Hex(4) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1524
-name: Hex(4)HexNAc(3)NeuAc(2)
-def: "Hex(4) HexNAc(3) NeuAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexnac=3&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1524]
-xref: record_id "1524"
-xref: delta_mono_mass "1839.640245"
-xref: delta_avge_mass "1840.6491"
-xref: delta_composition "Hex(4) HexNAc(3) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1840_mono_mass "1839.640245"
-xref: spec_1_neutral_loss_1840_avge_mass "1840.6491"
-xref: spec_1_neutral_loss_1840_flag "false"
-xref: spec_1_neutral_loss_1840_composition "Hex(4) HexNAc(3) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1525
-name: dHex(1)Hex(3)HexNAc(4)Pent(3)
-def: "DHex Hex(3) HexNAc(4) Pent(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexnac=4&pent=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1525]
-xref: record_id "1525"
-xref: delta_mono_mass "1840.660646"
-xref: delta_avge_mass "1841.6769"
-xref: delta_composition "dHex(1) Hex(3) HexNAc(4) Pent(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1841_mono_mass "1840.660646"
-xref: spec_1_neutral_loss_1841_avge_mass "1841.6769"
-xref: spec_1_neutral_loss_1841_flag "false"
-xref: spec_1_neutral_loss_1841_composition "dHex(1) Hex(3) HexNAc(4) Pent(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1526
-name: dHex(2)Hex(5)HexNAc(3)Pent(1)
-def: "DHex(2) Hex(5) HexNAc(3) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=5&hexnac=3&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1526]
-xref: record_id "1526"
-xref: delta_mono_mass "1843.660312"
-xref: delta_avge_mass "1844.6776"
-xref: delta_composition "dHex(2) Hex(5) HexNAc(3) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1844_mono_mass "1843.660312"
-xref: spec_1_neutral_loss_1844_avge_mass "1844.6776"
-xref: spec_1_neutral_loss_1844_flag "false"
-xref: spec_1_neutral_loss_1844_composition "dHex(2) Hex(5) HexNAc(3) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1527
-name: dHex(1)Hex(5)HexNAc(4)Sulf(1)
-def: "DHex Hex(5) HexNAc(4) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=5&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1527]
-xref: record_id "1527"
-xref: delta_mono_mass "1848.596331"
-xref: delta_avge_mass "1849.6775"
-xref: delta_composition "O(3) S dHex Hex(5) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:37:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1849_mono_mass "1848.596331"
-xref: spec_1_neutral_loss_1849_avge_mass "1849.6775"
-xref: spec_1_neutral_loss_1849_flag "false"
-xref: spec_1_neutral_loss_1849_composition "O(3) S dHex Hex(5) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1528
-name: dHex(2)Hex(3)HexNAc(4)Pent(2)
-def: "DHex(2) Hex(3) HexNAc(4) Pent(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=3&hexnac=4&pent=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1528]
-xref: record_id "1528"
-xref: delta_mono_mass "1854.676296"
-xref: delta_avge_mass "1855.7035"
-xref: delta_composition "dHex(2) Hex(3) HexNAc(4) Pent(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1855_mono_mass "1854.676296"
-xref: spec_1_neutral_loss_1855_avge_mass "1855.7035"
-xref: spec_1_neutral_loss_1855_flag "false"
-xref: spec_1_neutral_loss_1855_composition "dHex(2) Hex(3) HexNAc(4) Pent(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1529
-name: dHex(1)Hex(5)HexNAc(3)NeuAc(1)
-def: "DHex Hex(5) HexNAc(3) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=5&hexnac=3&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1529]
-xref: record_id "1529"
-xref: delta_mono_mass "1856.655561"
-xref: delta_avge_mass "1857.6763"
-xref: delta_composition "dHex(1) Hex(5) HexNAc(3) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1857_mono_mass "1856.655561"
-xref: spec_1_neutral_loss_1857_avge_mass "1857.6763"
-xref: spec_1_neutral_loss_1857_flag "false"
-xref: spec_1_neutral_loss_1857_composition "dHex(1) Hex(5) HexNAc(3) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1530
-name: Hex(3)HexNAc(6)Sulf(2)
-def: "Hex(3) HexNAc(6) Sulf(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=2&hex=3&hexnac=6&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1530]
-xref: record_id "1530"
-xref: delta_mono_mass "1864.548335"
-xref: delta_avge_mass "1865.7033"
-xref: delta_composition "O(6) S(2) Hex(3) HexNAc(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:37:39"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1865_mono_mass "1864.548335"
-xref: spec_1_neutral_loss_1865_avge_mass "1865.7033"
-xref: spec_1_neutral_loss_1865_flag "false"
-xref: spec_1_neutral_loss_1865_composition "O(6) S(2) Hex(3) HexNAc(6)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1531
-name: Hex(9)HexNAc(2)
-def: "M9/Man9." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=9&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1531]
-xref: record_id "1531"
-xref: delta_mono_mass "1864.634157"
-xref: delta_avge_mass "1865.6504"
-xref: delta_composition "Hex(9) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2020-08-02 11:48:38"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1865_mono_mass "1864.634157"
-xref: spec_1_neutral_loss_1865_avge_mass "1865.6504"
-xref: spec_1_neutral_loss_1865_flag "false"
-xref: spec_1_neutral_loss_1865_composition "Hex(9) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1532
-name: Hex(4)HexNAc(6)
-def: "Hex(4) HexNAc(6)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexnac=6&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1532]
-xref: record_id "1532"
-xref: delta_mono_mass "1866.68753"
-xref: delta_avge_mass "1867.7175"
-xref: delta_composition "Hex(4) HexNAc(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1867_mono_mass "1866.68753"
-xref: spec_1_neutral_loss_1867_avge_mass "1867.7175"
-xref: spec_1_neutral_loss_1867_flag "false"
-xref: spec_1_neutral_loss_1867_composition "Hex(4) HexNAc(6)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1533
-name: dHex(3)Hex(3)HexNAc(4)Pent(1)
-def: "DHex(3) Hex(3) HexNAc(4) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=3&hex=3&hexnac=4&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1533]
-xref: record_id "1533"
-xref: delta_mono_mass "1868.691946"
-xref: delta_avge_mass "1869.7301"
-xref: delta_composition "dHex(3) Hex(3) HexNAc(4) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1869_mono_mass "1868.691946"
-xref: spec_1_neutral_loss_1869_avge_mass "1869.7301"
-xref: spec_1_neutral_loss_1869_flag "false"
-xref: spec_1_neutral_loss_1869_composition "dHex(3) Hex(3) HexNAc(4) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1534
-name: dHex(1)Hex(5)HexNAc(3)NeuGc(1)
-def: "DHex Hex(5) HexNAc(3) NeuGc ---OR--- Hex(6) HexNAc(3) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=5&hexnac=3&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1534]
-xref: record_id "1534"
-xref: delta_mono_mass "1872.650475"
-xref: delta_avge_mass "1873.6757"
-xref: delta_composition "dHex Hex(5) HexNAc(3) NeuGc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-22 11:15:38"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1873_mono_mass "1872.650475"
-xref: spec_1_neutral_loss_1873_avge_mass "1873.6757"
-xref: spec_1_neutral_loss_1873_flag "false"
-xref: spec_1_neutral_loss_1873_composition "dHex Hex(5) HexNAc(3) NeuGc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1535
-name: dHex(2)Hex(4)HexNAc(4)Pent(1)
-def: "DHex(2) Hex(4) HexNAc(4) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=4&hexnac=4&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1535]
-xref: record_id "1535"
-xref: delta_mono_mass "1884.686861"
-xref: delta_avge_mass "1885.7295"
-xref: delta_composition "dHex(2) Hex(4) HexNAc(4) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1885_mono_mass "1884.686861"
-xref: spec_1_neutral_loss_1885_avge_mass "1885.7295"
-xref: spec_1_neutral_loss_1885_flag "false"
-xref: spec_1_neutral_loss_1885_composition "dHex(2) Hex(4) HexNAc(4) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1536
-name: dHex(1)Hex(4)HexNAc(5)Sulf(1)
-def: "DHex Hex(4) HexNAc(5) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=4&hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1536]
-xref: record_id "1536"
-xref: delta_mono_mass "1889.62288"
-xref: delta_avge_mass "1890.7294"
-xref: delta_composition "O(3) S dHex Hex(4) HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:37:53"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1890_mono_mass "1889.62288"
-xref: spec_1_neutral_loss_1890_avge_mass "1890.7294"
-xref: spec_1_neutral_loss_1890_flag "false"
-xref: spec_1_neutral_loss_1890_composition "O(3) S dHex Hex(4) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1537
-name: dHex(1)Hex(7)HexNAc(3)
-def: "DHex Hex(7) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=7&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1537]
-xref: record_id "1537"
-xref: delta_mono_mass "1889.665791"
-xref: delta_avge_mass "1890.703"
-xref: delta_composition "dHex(1) Hex(7) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1890_mono_mass "1889.665791"
-xref: spec_1_neutral_loss_1890_avge_mass "1890.703"
-xref: spec_1_neutral_loss_1890_flag "false"
-xref: spec_1_neutral_loss_1890_composition "dHex(1) Hex(7) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1538
-name: dHex(1)Hex(5)HexNAc(4)Pent(1)
-def: "DHex Hex(5) HexNAc(4) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=5&hexnac=4&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1538]
-xref: record_id "1538"
-xref: delta_mono_mass "1900.681776"
-xref: delta_avge_mass "1901.7289"
-xref: delta_composition "dHex(1) Hex(5) HexNAc(4) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1901_mono_mass "1900.681776"
-xref: spec_1_neutral_loss_1901_avge_mass "1901.7289"
-xref: spec_1_neutral_loss_1901_flag "false"
-xref: spec_1_neutral_loss_1901_composition "dHex(1) Hex(5) HexNAc(4) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1539
-name: dHex(1)Hex(5)HexA(1)HexNAc(3)Sulf(2)
-def: "DHex Hex(5) HexA HexNAc(3) Sulf(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=2&dhex=1&hex=5&hexa=1&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1539]
-xref: record_id "1539"
-xref: delta_mono_mass "1901.505861"
-xref: delta_avge_mass "1902.6723"
-xref: delta_composition "O(6) S(2) dHex Hex(5) HexA HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:38:08"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1902_mono_mass "1901.505861"
-xref: spec_1_neutral_loss_1902_avge_mass "1902.6723"
-xref: spec_1_neutral_loss_1902_flag "false"
-xref: spec_1_neutral_loss_1902_composition "O(6) S(2) dHex Hex(5) HexA HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1540
-name: Hex(3)HexNAc(7)
-def: "Hex(3) HexNAc(7)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=7&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1540]
-xref: record_id "1540"
-xref: delta_mono_mass "1907.714079"
-xref: delta_avge_mass "1908.7694"
-xref: delta_composition "Hex(3) HexNAc(7)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1908_mono_mass "1907.714079"
-xref: spec_1_neutral_loss_1908_avge_mass "1908.7694"
-xref: spec_1_neutral_loss_1908_flag "false"
-xref: spec_1_neutral_loss_1908_composition "Hex(3) HexNAc(7)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1541
-name: dHex(2)Hex(5)HexNAc(4)
-def: "DHex(2) Hex(5) HexNAc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=5&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1541]
-xref: record_id "1541"
-xref: delta_mono_mass "1914.697426"
-xref: delta_avge_mass "1915.7555"
-xref: delta_composition "dHex(2) Hex(5) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1915_mono_mass "1914.697426"
-xref: spec_1_neutral_loss_1915_avge_mass "1915.7555"
-xref: spec_1_neutral_loss_1915_flag "false"
-xref: spec_1_neutral_loss_1915_composition "dHex(2) Hex(5) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1542
-name: dHex(2)Hex(4)HexNAc(3)NeuAc(1)Sulf(1)
-def: "DHex(2) Hex(4) HexNAc(3) NeuAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=2&hex=4&hexnac=3&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1542]
-xref: record_id "1542"
-xref: delta_mono_mass "1920.617461"
-xref: delta_avge_mass "1921.7401"
-xref: delta_composition "O(3) S dHex(2) Hex(4) HexNAc(3) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:38:20"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1921_mono_mass "1920.617461"
-xref: spec_1_neutral_loss_1921_avge_mass "1921.7401"
-xref: spec_1_neutral_loss_1921_flag "false"
-xref: spec_1_neutral_loss_1921_composition "O(3) S dHex(2) Hex(4) HexNAc(3) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1543
-name: dHex(1)Hex(5)HexNAc(4)Sulf(2)
-def: "DHex Hex(5) HexNAc(4) Sulf(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=2&dhex=1&hex=5&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1543]
-xref: record_id "1543"
-xref: delta_mono_mass "1928.553146"
-xref: delta_avge_mass "1929.7407"
-xref: delta_composition "O(6) S(2) dHex Hex(5) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:39:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1929_mono_mass "1928.553146"
-xref: spec_1_neutral_loss_1929_avge_mass "1929.7407"
-xref: spec_1_neutral_loss_1929_flag "false"
-xref: spec_1_neutral_loss_1929_composition "O(6) S(2) dHex Hex(5) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1544
-name: dHex(1)Hex(5)HexNAc(4)Me(2)Pent(1)
-def: "DHex Hex(5) HexNAc(4) Me(2) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=5&hexnac=4&methyl=2&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1544]
-xref: record_id "1544"
-xref: delta_mono_mass "1928.713076"
-xref: delta_avge_mass "1929.7821"
-xref: delta_composition "dHex(1) Hex(5) HexNAc(4) Me(2) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1929_mono_mass "1928.713076"
-xref: spec_1_neutral_loss_1929_avge_mass "1929.7821"
-xref: spec_1_neutral_loss_1929_flag "false"
-xref: spec_1_neutral_loss_1929_composition "dHex(1) Hex(5) HexNAc(4) Me(2) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1545
-name: Hex(5)HexNAc(4)NeuGc(1)
-def: "Hex(5) HexNAc(4) NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=5&hexnac=4&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1545]
-xref: record_id "1545"
-xref: delta_mono_mass "1929.671939"
-xref: delta_avge_mass "1930.7271"
-xref: delta_composition "Hex(5) HexNAc(4) NeuGc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1930_mono_mass "1929.671939"
-xref: spec_1_neutral_loss_1930_avge_mass "1930.7271"
-xref: spec_1_neutral_loss_1930_flag "false"
-xref: spec_1_neutral_loss_1930_composition "Hex(5) HexNAc(4) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1546
-name: dHex(1)Hex(3)HexNAc(6)Sulf(1)
-def: "DHex Hex(3) HexNAc(6) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=3&hexnac=6&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1546]
-xref: record_id "1546"
-xref: delta_mono_mass "1930.64943"
-xref: delta_avge_mass "1931.7813"
-xref: delta_composition "O(3) S dHex Hex(3) HexNAc(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:39:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1931_mono_mass "1930.64943"
-xref: spec_1_neutral_loss_1931_avge_mass "1931.7813"
-xref: spec_1_neutral_loss_1931_flag "false"
-xref: spec_1_neutral_loss_1931_composition "O(3) S dHex Hex(3) HexNAc(6)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1547
-name: dHex(1)Hex(6)HexNAc(4)
-def: "DHex Hex(6) HexNAc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=6&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1547]
-xref: record_id "1547"
-xref: delta_mono_mass "1930.69234"
-xref: delta_avge_mass "1931.7549"
-xref: delta_composition "dHex(1) Hex(6) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1931_mono_mass "1930.69234"
-xref: spec_1_neutral_loss_1931_avge_mass "1931.7549"
-xref: spec_1_neutral_loss_1931_flag "false"
-xref: spec_1_neutral_loss_1931_composition "dHex(1) Hex(6) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1548
-name: dHex(1)Hex(5)HexNAc(3)NeuAc(1)Sulf(1)
-def: "DHex Hex(5) HexNAc(3) NeuAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=5&hexnac=3&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1548]
-xref: record_id "1548"
-xref: delta_mono_mass "1936.612375"
-xref: delta_avge_mass "1937.7395"
-xref: delta_composition "O(3) S dHex Hex(5) HexNAc(3) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:39:43"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1937_mono_mass "1936.612375"
-xref: spec_1_neutral_loss_1937_avge_mass "1937.7395"
-xref: spec_1_neutral_loss_1937_flag "false"
-xref: spec_1_neutral_loss_1937_composition "O(3) S dHex Hex(5) HexNAc(3) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1549
-name: Hex(7)HexNAc(4)
-def: "Hex(7) HexNAc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=7&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1549]
-xref: record_id "1549"
-xref: delta_mono_mass "1946.687255"
-xref: delta_avge_mass "1947.7543"
-xref: delta_composition "Hex(7) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1947_mono_mass "1946.687255"
-xref: spec_1_neutral_loss_1947_avge_mass "1947.7543"
-xref: spec_1_neutral_loss_1947_flag "false"
-xref: spec_1_neutral_loss_1947_composition "Hex(7) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1550
-name: dHex(1)Hex(5)HexNAc(3)NeuGc(1)Sulf(1)
-def: "DHex Hex(5) HexNAc(3) NeuGc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=5&hexnac=3&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1550]
-xref: record_id "1550"
-xref: delta_mono_mass "1952.60729"
-xref: delta_avge_mass "1953.7389"
-xref: delta_composition "O(3) S dHex Hex(5) HexNAc(3) NeuGc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:39:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1953_mono_mass "1952.60729"
-xref: spec_1_neutral_loss_1953_avge_mass "1953.7389"
-xref: spec_1_neutral_loss_1953_flag "false"
-xref: spec_1_neutral_loss_1953_composition "O(3) S dHex Hex(5) HexNAc(3) NeuGc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1551
-name: Hex(4)HexNAc(5)NeuAc(1)
-def: "Hex(4) HexNAc(5) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexnac=5&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1551]
-xref: record_id "1551"
-xref: delta_mono_mass "1954.703574"
-xref: delta_avge_mass "1955.7796"
-xref: delta_composition "Hex(4) HexNAc(5) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1955_mono_mass "1954.703574"
-xref: spec_1_neutral_loss_1955_avge_mass "1955.7796"
-xref: spec_1_neutral_loss_1955_flag "false"
-xref: spec_1_neutral_loss_1955_composition "Hex(4) HexNAc(5) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1552
-name: Hex(6)HexNAc(4)Me(3)Pent(1)
-def: "Hex(6) HexNAc(4) Me(3) Pent." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=6&hexnac=4&methyl=3&pent=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1552]
-xref: record_id "1552"
-xref: delta_mono_mass "1958.72364"
-xref: delta_avge_mass "1959.808"
-xref: delta_composition "Hex(6) HexNAc(4) Me(3) Pent(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1959_mono_mass "1958.72364"
-xref: spec_1_neutral_loss_1959_avge_mass "1959.808"
-xref: spec_1_neutral_loss_1959_flag "false"
-xref: spec_1_neutral_loss_1959_composition "Hex(6) HexNAc(4) Me(3) Pent(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1553
-name: dHex(1)Hex(7)HexNAc(3)Sulf(1)
-def: "DHex Hex(7) HexNAc(3) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=7&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1553]
-xref: record_id "1553"
-xref: delta_mono_mass "1969.622606"
-xref: delta_avge_mass "1970.7662"
-xref: delta_composition "O(3) S dHex Hex(7) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:40:07"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1970_mono_mass "1969.622606"
-xref: spec_1_neutral_loss_1970_avge_mass "1970.7662"
-xref: spec_1_neutral_loss_1970_flag "false"
-xref: spec_1_neutral_loss_1970_composition "O(3) S dHex Hex(7) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1554
-name: dHex(1)Hex(7)HexNAc(3)Phos(1)
-def: "DHex Hex(7) HexNAc(3) Phos." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=1&dhex=1&hex=7&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1554]
-xref: record_id "1554"
-xref: delta_mono_mass "1969.632122"
-xref: delta_avge_mass "1970.6829"
-xref: delta_composition "H O(3) P dHex Hex(7) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:44:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1970_mono_mass "1969.632122"
-xref: spec_1_neutral_loss_1970_avge_mass "1970.6829"
-xref: spec_1_neutral_loss_1970_flag "false"
-xref: spec_1_neutral_loss_1970_composition "H O(3) P dHex Hex(7) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1555
-name: dHex(1)Hex(5)HexNAc(5)
-def: "DHex Hex(5) HexNAc(5)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=5&hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1555]
-xref: record_id "1555"
-xref: delta_mono_mass "1971.718889"
-xref: delta_avge_mass "1972.8068"
-xref: delta_composition "dHex(1) Hex(5) HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1972_mono_mass "1971.718889"
-xref: spec_1_neutral_loss_1972_avge_mass "1972.8068"
-xref: spec_1_neutral_loss_1972_flag "false"
-xref: spec_1_neutral_loss_1972_composition "dHex(1) Hex(5) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1556
-name: dHex(1)Hex(4)HexNAc(4)NeuAc(1)Sulf(1)
-def: "DHex Hex(4) HexNAc(4) NeuAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=4&hexnac=4&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1556]
-xref: record_id "1556"
-xref: delta_mono_mass "1977.638925"
-xref: delta_avge_mass "1978.7915"
-xref: delta_composition "O(3) S dHex Hex(4) HexNAc(4) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:40:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1978_mono_mass "1977.638925"
-xref: spec_1_neutral_loss_1978_avge_mass "1978.7915"
-xref: spec_1_neutral_loss_1978_flag "false"
-xref: spec_1_neutral_loss_1978_composition "O(3) S dHex Hex(4) HexNAc(4) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1557
-name: dHex(3)Hex(4)HexNAc(4)Sulf(1)
-def: "DHex(3) Hex(4) HexNAc(4) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=3&hex=4&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1557]
-xref: record_id "1557"
-xref: delta_mono_mass "1978.659326"
-xref: delta_avge_mass "1979.8193"
-xref: delta_composition "O(3) S dHex(3) Hex(4) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:40:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1979_mono_mass "1978.659326"
-xref: spec_1_neutral_loss_1979_avge_mass "1979.8193"
-xref: spec_1_neutral_loss_1979_flag "false"
-xref: spec_1_neutral_loss_1979_composition "O(3) S dHex(3) Hex(4) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1558
-name: Hex(3)HexNAc(7)Sulf(1)
-def: "Hex(3) HexNAc(7) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=3&hexnac=7&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1558]
-xref: record_id "1558"
-xref: delta_mono_mass "1987.670893"
-xref: delta_avge_mass "1988.8326"
-xref: delta_composition "O(3) S Hex(3) HexNAc(7)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:40:39"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1988_mono_mass "1987.670893"
-xref: spec_1_neutral_loss_1988_avge_mass "1988.8326"
-xref: spec_1_neutral_loss_1988_flag "false"
-xref: spec_1_neutral_loss_1988_composition "O(3) S Hex(3) HexNAc(7)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1559
-name: Hex(6)HexNAc(5)
-def: "A3G3." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=6&hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1559]
-xref: record_id "1559"
-xref: delta_mono_mass "1987.713804"
-xref: delta_avge_mass "1988.8062"
-xref: delta_composition "Hex(6) HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2020-08-02 11:45:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1988_mono_mass "1987.713804"
-xref: spec_1_neutral_loss_1988_avge_mass "1988.8062"
-xref: spec_1_neutral_loss_1988_flag "false"
-xref: spec_1_neutral_loss_1988_composition "Hex(6) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1560
-name: Hex(5)HexNAc(4)NeuAc(1)Sulf(1)
-def: "Hex(5) HexNAc(4) NeuAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=5&hexnac=4&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1560]
-xref: record_id "1560"
-xref: delta_mono_mass "1993.633839"
-xref: delta_avge_mass "1994.7909"
-xref: delta_composition "O(3) S Hex(5) HexNAc(4) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:40:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1994_mono_mass "1993.633839"
-xref: spec_1_neutral_loss_1994_avge_mass "1994.7909"
-xref: spec_1_neutral_loss_1994_flag "false"
-xref: spec_1_neutral_loss_1994_composition "O(3) S Hex(5) HexNAc(4) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1561
-name: Hex(3)HexNAc(6)NeuAc(1)
-def: "Hex(3) HexNAc(6) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=6&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1561]
-xref: record_id "1561"
-xref: delta_mono_mass "1995.730123"
-xref: delta_avge_mass "1996.8315"
-xref: delta_composition "Hex(3) HexNAc(6) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1996_mono_mass "1995.730123"
-xref: spec_1_neutral_loss_1996_avge_mass "1996.8315"
-xref: spec_1_neutral_loss_1996_flag "false"
-xref: spec_1_neutral_loss_1996_composition "Hex(3) HexNAc(6) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1562
-name: dHex(2)Hex(3)HexNAc(6)
-def: "DHex(2) Hex(3) HexNAc(6)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=3&hexnac=6&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1562]
-xref: record_id "1562"
-xref: delta_mono_mass "1996.750524"
-xref: delta_avge_mass "1997.8593"
-xref: delta_composition "dHex(2) Hex(3) HexNAc(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1997_mono_mass "1996.750524"
-xref: spec_1_neutral_loss_1997_avge_mass "1997.8593"
-xref: spec_1_neutral_loss_1997_flag "false"
-xref: spec_1_neutral_loss_1997_composition "dHex(2) Hex(3) HexNAc(6)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1563
-name: Hex(1)HexNAc(1)NeuGc(1)
-def: "Hex HexNAc NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=1&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1563]
-xref: record_id "1563"
-xref: delta_mono_mass "672.222527"
-xref: delta_avge_mass "672.5871"
-xref: delta_composition "Hex(1) HexNAc(1) NeuGc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_673_mono_mass "672.222527"
-xref: spec_1_neutral_loss_673_avge_mass "672.5871"
-xref: spec_1_neutral_loss_673_flag "false"
-xref: spec_1_neutral_loss_673_composition "Hex(1) HexNAc(1) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_673_mono_mass "672.222527"
-xref: spec_1_neutral_loss_673_avge_mass "672.5871"
-xref: spec_1_neutral_loss_673_flag "false"
-xref: spec_1_neutral_loss_673_composition "Hex(1) HexNAc(1) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1564
-name: dHex(1)Hex(2)HexNAc(1)
-def: "DHex Hex(2) HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=2&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1564]
-xref: record_id "1564"
-xref: delta_mono_mass "673.242928"
-xref: delta_avge_mass "673.6149"
-xref: delta_composition "dHex(1) Hex(2) HexNAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_674_mono_mass "673.242928"
-xref: spec_1_neutral_loss_674_avge_mass "673.6149"
-xref: spec_1_neutral_loss_674_flag "false"
-xref: spec_1_neutral_loss_674_composition "dHex(1) Hex(2) HexNAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_674_mono_mass "673.242928"
-xref: spec_1_neutral_loss_674_avge_mass "673.6149"
-xref: spec_1_neutral_loss_674_flag "false"
-xref: spec_1_neutral_loss_674_composition "dHex(1) Hex(2) HexNAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1565
-name: HexNAc(3)Sulf(1)
-def: "HexNAc(3) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1565]
-xref: record_id "1565"
-xref: delta_mono_mass "689.194932"
-xref: delta_avge_mass "689.6408"
-xref: delta_composition "O(3) S HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:26:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_690_mono_mass "689.194932"
-xref: spec_1_neutral_loss_690_avge_mass "689.6408"
-xref: spec_1_neutral_loss_690_flag "false"
-xref: spec_1_neutral_loss_690_composition "O(3) S HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_690_mono_mass "689.194932"
-xref: spec_1_neutral_loss_690_avge_mass "689.6408"
-xref: spec_1_neutral_loss_690_flag "false"
-xref: spec_1_neutral_loss_690_composition "O(3) S HexNAc(3)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1566
-name: Hex(3)HexNAc(1)
-def: "Hex(3) HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1566]
-xref: record_id "1566"
-xref: delta_mono_mass "689.237843"
-xref: delta_avge_mass "689.6143"
-xref: delta_composition "Hex(3) HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-23 17:47:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_690_mono_mass "689.237843"
-xref: spec_1_neutral_loss_690_avge_mass "689.6143"
-xref: spec_1_neutral_loss_690_flag "false"
-xref: spec_1_neutral_loss_690_composition "Hex(3) HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_690_mono_mass "689.237843"
-xref: spec_1_neutral_loss_690_avge_mass "689.6143"
-xref: spec_1_neutral_loss_690_flag "false"
-xref: spec_1_neutral_loss_690_composition "Hex(3) HexNAc"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_690_mono_mass "689.237843"
-xref: spec_2_neutral_loss_690_avge_mass "689.6143"
-xref: spec_2_neutral_loss_690_flag "false"
-xref: spec_2_neutral_loss_690_composition "Hex(3) HexNAc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1567
-name: Hex(1)HexNAc(1)Kdn(1)Sulf(1)
-def: "Hex HexNAc Kdn Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=1&hexnac=1&kdn=1)mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1567]
-xref: record_id "1567"
-xref: delta_mono_mass "695.157878"
-xref: delta_avge_mass "695.599"
-xref: delta_composition "O(3) S Hex HexNAc Kdn"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:26:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_696_mono_mass "695.157878"
-xref: spec_1_neutral_loss_696_avge_mass "695.599"
-xref: spec_1_neutral_loss_696_flag "false"
-xref: spec_1_neutral_loss_696_composition "O(3) S Hex HexNAc Kdn"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_696_mono_mass "695.157878"
-xref: spec_1_neutral_loss_696_avge_mass "695.599"
-xref: spec_1_neutral_loss_696_flag "false"
-xref: spec_1_neutral_loss_696_composition "O(3) S Hex HexNAc Kdn"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1568
-name: HexNAc(2)NeuAc(1)
-def: "HexNAc(2) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hexnac=2&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1568]
-xref: record_id "1568"
-xref: delta_mono_mass "697.254162"
-xref: delta_avge_mass "697.6396"
-xref: delta_composition "HexNAc(2) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_698_mono_mass "697.254162"
-xref: spec_1_neutral_loss_698_avge_mass "697.6396"
-xref: spec_1_neutral_loss_698_flag "false"
-xref: spec_1_neutral_loss_698_composition "HexNAc(2) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_698_mono_mass "697.254162"
-xref: spec_1_neutral_loss_698_avge_mass "697.6396"
-xref: spec_1_neutral_loss_698_flag "false"
-xref: spec_1_neutral_loss_698_composition "HexNAc(2) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1570
-name: HexNAc(1)Kdn(2)
-def: "HexNAc Kdn(2) ---OR--- Hex(2) HexNAc HexA." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hexnac=1&kdn=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1570]
-xref: record_id "1570"
-xref: delta_mono_mass "703.217108"
-xref: delta_avge_mass "703.5978"
-xref: delta_composition "HexNAc Kdn(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-17 11:43:15"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_704_mono_mass "703.217108"
-xref: spec_1_neutral_loss_704_avge_mass "703.5978"
-xref: spec_1_neutral_loss_704_flag "false"
-xref: spec_1_neutral_loss_704_composition "HexNAc Kdn(2)"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_704_mono_mass "703.217108"
-xref: spec_1_neutral_loss_704_avge_mass "703.5978"
-xref: spec_1_neutral_loss_704_flag "false"
-xref: spec_1_neutral_loss_704_composition "HexNAc Kdn(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1571
-name: Hex(3)HexNAc(1)Me(1)
-def: "Hex(3) HexNAc Me." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=1&methyl=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1571]
-xref: record_id "1571"
-xref: delta_mono_mass "703.253493"
-xref: delta_avge_mass "703.6409"
-xref: delta_composition "Hex(3) HexNAc(1) Me(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_704_mono_mass "703.253493"
-xref: spec_1_neutral_loss_704_avge_mass "703.6409"
-xref: spec_1_neutral_loss_704_flag "false"
-xref: spec_1_neutral_loss_704_composition "Hex(3) HexNAc(1) Me(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_704_mono_mass "703.253493"
-xref: spec_1_neutral_loss_704_avge_mass "703.6409"
-xref: spec_1_neutral_loss_704_flag "false"
-xref: spec_1_neutral_loss_704_composition "Hex(3) HexNAc(1) Me(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1572
-name: Hex(2)HexA(1)Pent(1)Sulf(1)
-def: "Hex(2) HexA Pent Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&pent=1&hex=2&hexa=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1572]
-xref: record_id "1572"
-xref: delta_mono_mass "712.136808"
-xref: delta_avge_mass "712.5831"
-xref: delta_composition "O(3) S Pent Hex(2) HexA"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:27:09"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_713_mono_mass "712.136808"
-xref: spec_1_neutral_loss_713_avge_mass "712.5831"
-xref: spec_1_neutral_loss_713_flag "false"
-xref: spec_1_neutral_loss_713_composition "O(3) S Pent Hex(2) HexA"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_713_mono_mass "712.136808"
-xref: spec_1_neutral_loss_713_avge_mass "712.5831"
-xref: spec_1_neutral_loss_713_flag "false"
-xref: spec_1_neutral_loss_713_composition "O(3) S Pent Hex(2) HexA"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1573
-name: HexNAc(2)NeuGc(1)
-def: "HexNAc(2) NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hexnac=2&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1573]
-xref: record_id "1573"
-xref: delta_mono_mass "713.249076"
-xref: delta_avge_mass "713.639"
-xref: delta_composition "HexNAc(2) NeuGc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_714_mono_mass "713.249076"
-xref: spec_1_neutral_loss_714_avge_mass "713.639"
-xref: spec_1_neutral_loss_714_flag "false"
-xref: spec_1_neutral_loss_714_composition "HexNAc(2) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_714_mono_mass "713.249076"
-xref: spec_1_neutral_loss_714_avge_mass "713.639"
-xref: spec_1_neutral_loss_714_flag "false"
-xref: spec_1_neutral_loss_714_composition "HexNAc(2) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1575
-name: Hex(4)Phos(1)
-def: "Hex(4) Phos." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=1&hex=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1575]
-xref: record_id "1575"
-xref: delta_mono_mass "728.177625"
-xref: delta_avge_mass "728.5423"
-xref: delta_composition "H O(3) P Hex(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:42:07"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_729_mono_mass "728.177625"
-xref: spec_1_neutral_loss_729_avge_mass "728.5423"
-xref: spec_1_neutral_loss_729_flag "false"
-xref: spec_1_neutral_loss_729_composition "H O(3) P Hex(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_729_mono_mass "728.177625"
-xref: spec_1_neutral_loss_729_avge_mass "728.5423"
-xref: spec_1_neutral_loss_729_flag "false"
-xref: spec_1_neutral_loss_729_composition "H O(3) P Hex(4)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1577
-name: Hex(1)HexNAc(1)NeuAc(1)Sulf(1)
-def: "Hex HexNAc NeuAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=1&hexnac=1&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1577]
-xref: record_id "1577"
-xref: delta_mono_mass "736.184427"
-xref: delta_avge_mass "736.6509"
-xref: delta_composition "O(3) S Hex HexNAc NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:27:24"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_737_mono_mass "736.184427"
-xref: spec_1_neutral_loss_737_avge_mass "736.6509"
-xref: spec_1_neutral_loss_737_flag "false"
-xref: spec_1_neutral_loss_737_composition "O(3) S Hex HexNAc NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_737_mono_mass "736.184427"
-xref: spec_1_neutral_loss_737_avge_mass "736.6509"
-xref: spec_1_neutral_loss_737_flag "false"
-xref: spec_1_neutral_loss_737_composition "O(3) S Hex HexNAc NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1578
-name: Hex(1)HexA(1)HexNAc(2)
-def: "Hex HexA HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexa=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1578]
-xref: record_id "1578"
-xref: delta_mono_mass "744.243657"
-xref: delta_avge_mass "744.6498"
-xref: delta_composition "Hex(1) HexA(1) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_745_mono_mass "744.243657"
-xref: spec_1_neutral_loss_745_avge_mass "744.6498"
-xref: spec_1_neutral_loss_745_flag "false"
-xref: spec_1_neutral_loss_745_composition "Hex(1) HexA(1) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_745_mono_mass "744.243657"
-xref: spec_1_neutral_loss_745_avge_mass "744.6498"
-xref: spec_1_neutral_loss_745_flag "false"
-xref: spec_1_neutral_loss_745_composition "Hex(1) HexA(1) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1579
-name: dHex(1)Hex(2)HexNAc(1)Sulf(1)
-def: "DHex Hex(2) HexNAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=2&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1579]
-xref: record_id "1579"
-xref: delta_mono_mass "753.199743"
-xref: delta_avge_mass "753.6781"
-xref: delta_composition "O(3) S dHex Hex(2) HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:27:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_754_mono_mass "753.199743"
-xref: spec_1_neutral_loss_754_avge_mass "753.6781"
-xref: spec_1_neutral_loss_754_flag "false"
-xref: spec_1_neutral_loss_754_composition "O(3) S dHex Hex(2) HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_754_mono_mass "753.199743"
-xref: spec_1_neutral_loss_754_avge_mass "753.6781"
-xref: spec_1_neutral_loss_754_flag "false"
-xref: spec_1_neutral_loss_754_composition "O(3) S dHex Hex(2) HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1580
-name: dHex(1)HexNAc(3)
-def: "DHex HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1580]
-xref: record_id "1580"
-xref: delta_mono_mass "755.296027"
-xref: delta_avge_mass "755.7188"
-xref: delta_composition "dHex(1) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_756_mono_mass "755.296027"
-xref: spec_1_neutral_loss_756_avge_mass "755.7188"
-xref: spec_1_neutral_loss_756_flag "false"
-xref: spec_1_neutral_loss_756_composition "dHex(1) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_756_mono_mass "755.296027"
-xref: spec_1_neutral_loss_756_avge_mass "755.7188"
-xref: spec_1_neutral_loss_756_flag "false"
-xref: spec_1_neutral_loss_756_composition "dHex(1) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1581
-name: dHex(1)Hex(1)HexNAc(1)Kdn(1)
-def: "DHex Hex HexNAc Kdn ---OR--- Hex(2) dHex NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=1&hexnac=1&kdn=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1581]
-xref: record_id "1581"
-xref: delta_mono_mass "761.258973"
-xref: delta_avge_mass "761.677"
-xref: delta_composition "dHex Hex HexNAc Kdn"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-17 11:43:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_762_mono_mass "761.258973"
-xref: spec_1_neutral_loss_762_avge_mass "761.677"
-xref: spec_1_neutral_loss_762_flag "false"
-xref: spec_1_neutral_loss_762_composition "dHex Hex HexNAc Kdn"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_762_mono_mass "761.258973"
-xref: spec_1_neutral_loss_762_avge_mass "761.677"
-xref: spec_1_neutral_loss_762_flag "false"
-xref: spec_1_neutral_loss_762_composition "dHex Hex HexNAc Kdn"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1582
-name: Hex(1)HexNAc(3)
-def: "Hex HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1582]
-xref: record_id "1582"
-xref: delta_mono_mass "771.290941"
-xref: delta_avge_mass "771.7182"
-xref: delta_composition "Hex(1) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_772_mono_mass "771.290941"
-xref: spec_1_neutral_loss_772_avge_mass "771.7182"
-xref: spec_1_neutral_loss_772_flag "false"
-xref: spec_1_neutral_loss_772_composition "Hex(1) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_772_mono_mass "771.290941"
-xref: spec_1_neutral_loss_772_avge_mass "771.7182"
-xref: spec_1_neutral_loss_772_flag "false"
-xref: spec_1_neutral_loss_772_composition "Hex(1) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1583
-name: HexNAc(2)NeuAc(1)Sulf(1)
-def: "HexNAc(2) NeuAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hexnac=2&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1583]
-xref: record_id "1583"
-xref: delta_mono_mass "777.210976"
-xref: delta_avge_mass "777.7028"
-xref: delta_composition "O(3) S HexNAc(2) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:27:46"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_778_mono_mass "777.210976"
-xref: spec_1_neutral_loss_778_avge_mass "777.7028"
-xref: spec_1_neutral_loss_778_flag "false"
-xref: spec_1_neutral_loss_778_composition "O(3) S HexNAc(2) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_778_mono_mass "777.210976"
-xref: spec_1_neutral_loss_778_avge_mass "777.7028"
-xref: spec_1_neutral_loss_778_flag "false"
-xref: spec_1_neutral_loss_778_composition "O(3) S HexNAc(2) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1584
-name: dHex(2)Hex(3)
-def: "DHex(2) Hex(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1584]
-xref: record_id "1584"
-xref: delta_mono_mass "778.274288"
-xref: delta_avge_mass "778.7042"
-xref: delta_composition "dHex(2) Hex(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_779_mono_mass "778.274288"
-xref: spec_1_neutral_loss_779_avge_mass "778.7042"
-xref: spec_1_neutral_loss_779_flag "false"
-xref: spec_1_neutral_loss_779_composition "dHex(2) Hex(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_779_mono_mass "778.274288"
-xref: spec_1_neutral_loss_779_avge_mass "778.7042"
-xref: spec_1_neutral_loss_779_flag "false"
-xref: spec_1_neutral_loss_779_composition "dHex(2) Hex(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1585
-name: Hex(2)HexA(1)HexNAc(1)Sulf(1)
-def: "Hex(2) HexA HexNAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=2&hexa=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1585]
-xref: record_id "1585"
-xref: delta_mono_mass "783.173922"
-xref: delta_avge_mass "783.661"
-xref: delta_composition "O(3) S Hex(2) HexA HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:28:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_784_mono_mass "783.173922"
-xref: spec_1_neutral_loss_784_avge_mass "783.661"
-xref: spec_1_neutral_loss_784_flag "false"
-xref: spec_1_neutral_loss_784_composition "O(3) S Hex(2) HexA HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_784_mono_mass "783.173922"
-xref: spec_1_neutral_loss_784_avge_mass "783.661"
-xref: spec_1_neutral_loss_784_flag "false"
-xref: spec_1_neutral_loss_784_composition "O(3) S Hex(2) HexA HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1586
-name: dHex(2)Hex(2)HexA(1)
-def: "DHex(2) Hex(2) HexA." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=2&hexa=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1586]
-xref: record_id "1586"
-xref: delta_mono_mass "792.253553"
-xref: delta_avge_mass "792.6877"
-xref: delta_composition "dHex(2) Hex(2) HexA(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_793_mono_mass "792.253553"
-xref: spec_1_neutral_loss_793_avge_mass "792.6877"
-xref: spec_1_neutral_loss_793_flag "false"
-xref: spec_1_neutral_loss_793_composition "dHex(2) Hex(2) HexA(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_793_mono_mass "792.253553"
-xref: spec_1_neutral_loss_793_avge_mass "792.6877"
-xref: spec_1_neutral_loss_793_flag "false"
-xref: spec_1_neutral_loss_793_composition "dHex(2) Hex(2) HexA(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1587
-name: dHex(1)Hex(1)HexNAc(2)Sulf(1)
-def: "DHex Hex HexNAc(2) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1587]
-xref: record_id "1587"
-xref: delta_mono_mass "794.226292"
-xref: delta_avge_mass "794.73"
-xref: delta_composition "O(3) S dHex Hex HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:28:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_795_mono_mass "794.226292"
-xref: spec_1_neutral_loss_795_avge_mass "794.73"
-xref: spec_1_neutral_loss_795_flag "false"
-xref: spec_1_neutral_loss_795_composition "O(3) S dHex Hex HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_795_mono_mass "794.226292"
-xref: spec_1_neutral_loss_795_avge_mass "794.73"
-xref: spec_1_neutral_loss_795_flag "false"
-xref: spec_1_neutral_loss_795_composition "O(3) S dHex Hex HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1588
-name: dHex(1)Hex(1)HexNAc(1)NeuAc(1)
-def: "DHex Hex HexNAc NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=1&hexnac=1&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1588]
-xref: record_id "1588"
-xref: delta_mono_mass "802.285522"
-xref: delta_avge_mass "802.7289"
-xref: delta_composition "dHex(1) Hex(1) HexNAc(1) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_803_mono_mass "802.285522"
-xref: spec_1_neutral_loss_803_avge_mass "802.7289"
-xref: spec_1_neutral_loss_803_flag "false"
-xref: spec_1_neutral_loss_803_composition "dHex(1) Hex(1) HexNAc(1) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_803_mono_mass "802.285522"
-xref: spec_1_neutral_loss_803_avge_mass "802.7289"
-xref: spec_1_neutral_loss_803_flag "false"
-xref: spec_1_neutral_loss_803_composition "dHex(1) Hex(1) HexNAc(1) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1589
-name: Hex(2)HexNAc(2)Sulf(1)
-def: "Hex(2) HexNAc(2) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=2&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1589]
-xref: record_id "1589"
-xref: delta_mono_mass "810.221207"
-xref: delta_avge_mass "810.7294"
-xref: delta_composition "O(3) S Hex(2) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:28:21"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_811_mono_mass "810.221207"
-xref: spec_1_neutral_loss_811_avge_mass "810.7294"
-xref: spec_1_neutral_loss_811_flag "false"
-xref: spec_1_neutral_loss_811_composition "O(3) S Hex(2) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_811_mono_mass "810.221207"
-xref: spec_1_neutral_loss_811_avge_mass "810.7294"
-xref: spec_1_neutral_loss_811_flag "false"
-xref: spec_1_neutral_loss_811_composition "O(3) S Hex(2) HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1590
-name: Hex(5)
-def: "Hex(5)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1590]
-xref: record_id "1590"
-xref: delta_mono_mass "810.264117"
-xref: delta_avge_mass "810.703"
-xref: delta_composition "Hex(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_811_mono_mass "810.264117"
-xref: spec_1_neutral_loss_811_avge_mass "810.703"
-xref: spec_1_neutral_loss_811_flag "false"
-xref: spec_1_neutral_loss_811_composition "Hex(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_811_mono_mass "810.264117"
-xref: spec_1_neutral_loss_811_avge_mass "810.703"
-xref: spec_1_neutral_loss_811_flag "false"
-xref: spec_1_neutral_loss_811_composition "Hex(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1591
-name: HexNAc(4)
-def: "HexNAc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1591]
-xref: record_id "1591"
-xref: delta_mono_mass "812.31749"
-xref: delta_avge_mass "812.7701"
-xref: delta_composition "HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_813_mono_mass "812.31749"
-xref: spec_1_neutral_loss_813_avge_mass "812.7701"
-xref: spec_1_neutral_loss_813_flag "false"
-xref: spec_1_neutral_loss_813_composition "HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_813_mono_mass "812.31749"
-xref: spec_1_neutral_loss_813_avge_mass "812.7701"
-xref: spec_1_neutral_loss_813_flag "false"
-xref: spec_1_neutral_loss_813_composition "HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1592
-name: HexNAc(1)NeuGc(2)
-def: "HexNAc NeuGc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hexnac=1&neugc=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1592]
-xref: record_id "1592"
-xref: delta_mono_mass "817.260035"
-xref: delta_avge_mass "817.7005"
-xref: delta_composition "HexNAc(1) NeuGc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_818_mono_mass "817.260035"
-xref: spec_1_neutral_loss_818_avge_mass "817.7005"
-xref: spec_1_neutral_loss_818_flag "false"
-xref: spec_1_neutral_loss_818_composition "HexNAc(1) NeuGc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_818_mono_mass "817.260035"
-xref: spec_1_neutral_loss_818_avge_mass "817.7005"
-xref: spec_1_neutral_loss_818_flag "false"
-xref: spec_1_neutral_loss_818_composition "HexNAc(1) NeuGc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1593
-name: dHex(1)Hex(1)HexNAc(1)NeuGc(1)
-def: "DHex Hex HexNAc NeuGc ---OR--- Hex(2) HexNAc NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=1&hexnac=1&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1593]
-xref: record_id "1593"
-xref: delta_mono_mass "818.280436"
-xref: delta_avge_mass "818.7283"
-xref: delta_composition "dHex Hex HexNAc NeuGc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-17 11:43:38"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_819_mono_mass "818.280436"
-xref: spec_1_neutral_loss_819_avge_mass "818.7283"
-xref: spec_1_neutral_loss_819_flag "false"
-xref: spec_1_neutral_loss_819_composition "dHex Hex HexNAc NeuGc"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_819_mono_mass "818.280436"
-xref: spec_1_neutral_loss_819_avge_mass "818.7283"
-xref: spec_1_neutral_loss_819_flag "false"
-xref: spec_1_neutral_loss_819_composition "dHex Hex HexNAc NeuGc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1594
-name: dHex(2)Hex(2)HexNAc(1)
-def: "DHex(2) Hex(2) HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=2&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1594]
-xref: record_id "1594"
-xref: delta_mono_mass "819.300837"
-xref: delta_avge_mass "819.7561"
-xref: delta_composition "dHex(2) Hex(2) HexNAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_820_mono_mass "819.300837"
-xref: spec_1_neutral_loss_820_avge_mass "819.7561"
-xref: spec_1_neutral_loss_820_flag "false"
-xref: spec_1_neutral_loss_820_composition "dHex(2) Hex(2) HexNAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_820_mono_mass "819.300837"
-xref: spec_1_neutral_loss_820_avge_mass "819.7561"
-xref: spec_1_neutral_loss_820_flag "false"
-xref: spec_1_neutral_loss_820_composition "dHex(2) Hex(2) HexNAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1595
-name: Hex(2)HexNAc(1)NeuGc(1)
-def: "Hex(2) HexNAc NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=1&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1595]
-xref: record_id "1595"
-xref: delta_mono_mass "834.275351"
-xref: delta_avge_mass "834.7277"
-xref: delta_composition "Hex(2) HexNAc(1) NeuGc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_835_mono_mass "834.275351"
-xref: spec_1_neutral_loss_835_avge_mass "834.7277"
-xref: spec_1_neutral_loss_835_flag "false"
-xref: spec_1_neutral_loss_835_composition "Hex(2) HexNAc(1) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_835_mono_mass "834.275351"
-xref: spec_1_neutral_loss_835_avge_mass "834.7277"
-xref: spec_1_neutral_loss_835_flag "false"
-xref: spec_1_neutral_loss_835_composition "Hex(2) HexNAc(1) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1596
-name: dHex(1)Hex(3)HexNAc(1)
-def: "DHex Hex(3) HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1596]
-xref: record_id "1596"
-xref: delta_mono_mass "835.295752"
-xref: delta_avge_mass "835.7555"
-xref: delta_composition "dHex(1) Hex(3) HexNAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_836_mono_mass "835.295752"
-xref: spec_1_neutral_loss_836_avge_mass "835.7555"
-xref: spec_1_neutral_loss_836_flag "false"
-xref: spec_1_neutral_loss_836_composition "dHex(1) Hex(3) HexNAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_836_mono_mass "835.295752"
-xref: spec_1_neutral_loss_836_avge_mass "835.7555"
-xref: spec_1_neutral_loss_836_flag "false"
-xref: spec_1_neutral_loss_836_composition "dHex(1) Hex(3) HexNAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1597
-name: dHex(1)Hex(2)HexA(1)HexNAc(1)
-def: "DHex Hex(2) HexA HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=2&hexa=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1597]
-xref: record_id "1597"
-xref: delta_mono_mass "849.275017"
-xref: delta_avge_mass "849.739"
-xref: delta_composition "dHex(1) Hex(2) HexA(1) HexNAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_850_mono_mass "849.275017"
-xref: spec_1_neutral_loss_850_avge_mass "849.739"
-xref: spec_1_neutral_loss_850_flag "false"
-xref: spec_1_neutral_loss_850_composition "dHex(1) Hex(2) HexA(1) HexNAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_850_mono_mass "849.275017"
-xref: spec_1_neutral_loss_850_avge_mass "849.739"
-xref: spec_1_neutral_loss_850_flag "false"
-xref: spec_1_neutral_loss_850_composition "dHex(1) Hex(2) HexA(1) HexNAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1598
-name: Hex(1)HexNAc(3)Sulf(1)
-def: "Hex HexNAc(3) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=1&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1598]
-xref: record_id "1598"
-xref: delta_mono_mass "851.247756"
-xref: delta_avge_mass "851.7814"
-xref: delta_composition "O(3) S Hex HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:28:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_852_mono_mass "851.247756"
-xref: spec_1_neutral_loss_852_avge_mass "851.7814"
-xref: spec_1_neutral_loss_852_flag "false"
-xref: spec_1_neutral_loss_852_composition "O(3) S Hex HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_852_mono_mass "851.247756"
-xref: spec_1_neutral_loss_852_avge_mass "851.7814"
-xref: spec_1_neutral_loss_852_flag "false"
-xref: spec_1_neutral_loss_852_composition "O(3) S Hex HexNAc(3)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1599
-name: Hex(4)HexNAc(1)
-def: "Hex(4) HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1599]
-xref: record_id "1599"
-xref: delta_mono_mass "851.290667"
-xref: delta_avge_mass "851.7549"
-xref: delta_composition "Hex(4) HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-24 10:39:59"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_852_mono_mass "851.290667"
-xref: spec_1_neutral_loss_852_avge_mass "851.7549"
-xref: spec_1_neutral_loss_852_flag "false"
-xref: spec_1_neutral_loss_852_composition "Hex(4) HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_852_mono_mass "851.290667"
-xref: spec_1_neutral_loss_852_avge_mass "851.7549"
-xref: spec_1_neutral_loss_852_flag "false"
-xref: spec_1_neutral_loss_852_composition "Hex(4) HexNAc"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_852_mono_mass "851.290667"
-xref: spec_2_neutral_loss_852_avge_mass "851.7549"
-xref: spec_2_neutral_loss_852_flag "false"
-xref: spec_2_neutral_loss_852_composition "Hex(4) HexNAc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1600
-name: Hex(1)HexNAc(2)NeuAc(1)
-def: "Hex HexNAc(2) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=2&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1600]
-xref: record_id "1600"
-xref: delta_mono_mass "859.306985"
-xref: delta_avge_mass "859.7802"
-xref: delta_composition "Hex(1) HexNAc(2) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_860_mono_mass "859.306985"
-xref: spec_1_neutral_loss_860_avge_mass "859.7802"
-xref: spec_1_neutral_loss_860_flag "false"
-xref: spec_1_neutral_loss_860_composition "Hex(1) HexNAc(2) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_860_mono_mass "859.306985"
-xref: spec_1_neutral_loss_860_avge_mass "859.7802"
-xref: spec_1_neutral_loss_860_flag "false"
-xref: spec_1_neutral_loss_860_composition "Hex(1) HexNAc(2) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1602
-name: Hex(1)HexNAc(2)NeuGc(1)
-def: "Hex HexNAc(2) NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=2&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1602]
-xref: record_id "1602"
-xref: delta_mono_mass "875.3019"
-xref: delta_avge_mass "875.7796"
-xref: delta_composition "Hex(1) HexNAc(2) NeuGc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_876_mono_mass "875.3019"
-xref: spec_1_neutral_loss_876_avge_mass "875.7796"
-xref: spec_1_neutral_loss_876_flag "false"
-xref: spec_1_neutral_loss_876_composition "Hex(1) HexNAc(2) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_876_mono_mass "875.3019"
-xref: spec_1_neutral_loss_876_avge_mass "875.7796"
-xref: spec_1_neutral_loss_876_flag "false"
-xref: spec_1_neutral_loss_876_composition "Hex(1) HexNAc(2) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1604
-name: Hex(5)Phos(1)
-def: "Hex(5) Phos." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=1&hex=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1604]
-xref: record_id "1604"
-xref: delta_mono_mass "890.230448"
-xref: delta_avge_mass "890.6829"
-xref: delta_composition "H O(3) P Hex(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:42:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_891_mono_mass "890.230448"
-xref: spec_1_neutral_loss_891_avge_mass "890.6829"
-xref: spec_1_neutral_loss_891_flag "false"
-xref: spec_1_neutral_loss_891_composition "H O(3) P Hex(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_891_mono_mass "890.230448"
-xref: spec_1_neutral_loss_891_avge_mass "890.6829"
-xref: spec_1_neutral_loss_891_flag "false"
-xref: spec_1_neutral_loss_891_composition "H O(3) P Hex(5)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1606
-name: dHex(2)Hex(1)HexNAc(1)Kdn(1)
-def: "DHex(2) Hex HexNAc Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=1&hexnac=1&kdn=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1606]
-xref: record_id "1606"
-xref: delta_mono_mass "907.316881"
-xref: delta_avge_mass "907.8182"
-xref: delta_composition "dHex(2) Hex HexNAc Kdn"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 15:57:48"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_908_mono_mass "907.316881"
-xref: spec_1_neutral_loss_908_avge_mass "907.8182"
-xref: spec_1_neutral_loss_908_flag "false"
-xref: spec_1_neutral_loss_908_composition "dHex(2) Hex HexNAc Kdn"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_908_mono_mass "907.316881"
-xref: spec_1_neutral_loss_908_avge_mass "907.8182"
-xref: spec_1_neutral_loss_908_flag "false"
-xref: spec_1_neutral_loss_908_composition "dHex(2) Hex HexNAc Kdn"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1607
-name: dHex(1)Hex(3)HexNAc(1)Sulf(1)
-def: "DHex Hex(3) HexNAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=3&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1607]
-xref: record_id "1607"
-xref: delta_mono_mass "915.252567"
-xref: delta_avge_mass "915.8187"
-xref: delta_composition "O(3) S dHex Hex(3) HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:28:48"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_916_mono_mass "915.252567"
-xref: spec_1_neutral_loss_916_avge_mass "915.8187"
-xref: spec_1_neutral_loss_916_flag "false"
-xref: spec_1_neutral_loss_916_composition "O(3) S dHex Hex(3) HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_916_mono_mass "915.252567"
-xref: spec_1_neutral_loss_916_avge_mass "915.8187"
-xref: spec_1_neutral_loss_916_flag "false"
-xref: spec_1_neutral_loss_916_composition "O(3) S dHex Hex(3) HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1608
-name: dHex(1)Hex(1)HexNAc(3)
-def: "DHex Hex HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=1&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1608]
-xref: record_id "1608"
-xref: delta_mono_mass "917.34885"
-xref: delta_avge_mass "917.8594"
-xref: delta_composition "dHex(1) Hex(1) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_918_mono_mass "917.34885"
-xref: spec_1_neutral_loss_918_avge_mass "917.8594"
-xref: spec_1_neutral_loss_918_flag "false"
-xref: spec_1_neutral_loss_918_composition "dHex(1) Hex(1) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_918_mono_mass "917.34885"
-xref: spec_1_neutral_loss_918_avge_mass "917.8594"
-xref: spec_1_neutral_loss_918_flag "false"
-xref: spec_1_neutral_loss_918_composition "dHex(1) Hex(1) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1609
-name: dHex(1)Hex(2)HexA(1)HexNAc(1)Sulf(1)
-def: "DHex Hex(2) HexA HexNAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=2&hexa=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1609]
-xref: record_id "1609"
-xref: delta_mono_mass "929.231831"
-xref: delta_avge_mass "929.8022"
-xref: delta_composition "O(3) S dHex Hex(2) HexA HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:28:59"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_930_mono_mass "929.231831"
-xref: spec_1_neutral_loss_930_avge_mass "929.8022"
-xref: spec_1_neutral_loss_930_flag "false"
-xref: spec_1_neutral_loss_930_composition "O(3) S dHex Hex(2) HexA HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_930_mono_mass "929.231831"
-xref: spec_1_neutral_loss_930_avge_mass "929.8022"
-xref: spec_1_neutral_loss_930_flag "false"
-xref: spec_1_neutral_loss_930_composition "O(3) S dHex Hex(2) HexA HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1610
-name: Hex(2)HexNAc(3)
-def: "Hex(2) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1610]
-xref: record_id "1610"
-xref: delta_mono_mass "933.343765"
-xref: delta_avge_mass "933.8588"
-xref: delta_composition "Hex(2) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-24 10:43:39"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_934_mono_mass "933.343765"
-xref: spec_1_neutral_loss_934_avge_mass "933.8588"
-xref: spec_1_neutral_loss_934_flag "false"
-xref: spec_1_neutral_loss_934_composition "Hex(2) HexNAc(3)"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_934_mono_mass "933.343765"
-xref: spec_1_neutral_loss_934_avge_mass "933.8588"
-xref: spec_1_neutral_loss_934_flag "false"
-xref: spec_1_neutral_loss_934_composition "Hex(2) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_934_mono_mass "933.343765"
-xref: spec_2_neutral_loss_934_avge_mass "933.8588"
-xref: spec_2_neutral_loss_934_flag "false"
-xref: spec_2_neutral_loss_934_composition "Hex(2) HexNAc(3)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1611
-name: Hex(1)HexNAc(2)NeuAc(1)Sulf(1)
-def: "Hex HexNAc(2) NeuAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=1&hexnac=2&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1611]
-xref: record_id "1611"
-xref: delta_mono_mass "939.2638"
-xref: delta_avge_mass "939.8434"
-xref: delta_composition "O(3) S Hex HexNAc(2) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:29:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_940_mono_mass "939.2638"
-xref: spec_1_neutral_loss_940_avge_mass "939.8434"
-xref: spec_1_neutral_loss_940_flag "false"
-xref: spec_1_neutral_loss_940_composition "O(3) S Hex HexNAc(2) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_940_mono_mass "939.2638"
-xref: spec_1_neutral_loss_940_avge_mass "939.8434"
-xref: spec_1_neutral_loss_940_flag "false"
-xref: spec_1_neutral_loss_940_composition "O(3) S Hex HexNAc(2) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1612
-name: dHex(2)Hex(4)
-def: "DHex(2) Hex(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1612]
-xref: record_id "1612"
-xref: delta_mono_mass "940.327112"
-xref: delta_avge_mass "940.8448"
-xref: delta_composition "dHex(2) Hex(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_941_mono_mass "940.327112"
-xref: spec_1_neutral_loss_941_avge_mass "940.8448"
-xref: spec_1_neutral_loss_941_flag "false"
-xref: spec_1_neutral_loss_941_composition "dHex(2) Hex(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_941_mono_mass "940.327112"
-xref: spec_1_neutral_loss_941_avge_mass "940.8448"
-xref: spec_1_neutral_loss_941_flag "false"
-xref: spec_1_neutral_loss_941_composition "dHex(2) Hex(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1614
-name: dHex(2)HexNAc(2)Kdn(1)
-def: "DHex(2) HexNAc(2) Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hexnac=2&kdn=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1614]
-xref: record_id "1614"
-xref: delta_mono_mass "948.34343"
-xref: delta_avge_mass "948.8701"
-xref: delta_composition "dHex(2) HexNAc(2) Kdn"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 15:57:42"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_949_mono_mass "948.34343"
-xref: spec_1_neutral_loss_949_avge_mass "948.8701"
-xref: spec_1_neutral_loss_949_flag "false"
-xref: spec_1_neutral_loss_949_composition "dHex(2) HexNAc(2) Kdn"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_949_mono_mass "948.34343"
-xref: spec_1_neutral_loss_949_avge_mass "948.8701"
-xref: spec_1_neutral_loss_949_flag "false"
-xref: spec_1_neutral_loss_949_composition "dHex(2) HexNAc(2) Kdn"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1615
-name: dHex(1)Hex(2)HexNAc(2)Sulf(1)
-def: "DHex Hex(2) HexNAc(2) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=2&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1615]
-xref: record_id "1615"
-xref: delta_mono_mass "956.279116"
-xref: delta_avge_mass "956.8706"
-xref: delta_composition "O(3) S dHex Hex(2) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:29:22"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_957_mono_mass "956.279116"
-xref: spec_1_neutral_loss_957_avge_mass "956.8706"
-xref: spec_1_neutral_loss_957_flag "false"
-xref: spec_1_neutral_loss_957_composition "O(3) S dHex Hex(2) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_957_mono_mass "956.279116"
-xref: spec_1_neutral_loss_957_avge_mass "956.8706"
-xref: spec_1_neutral_loss_957_flag "false"
-xref: spec_1_neutral_loss_957_composition "O(3) S dHex Hex(2) HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1616
-name: dHex(1)HexNAc(4)
-def: "DHex HexNAc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1616]
-xref: record_id "1616"
-xref: delta_mono_mass "958.375399"
-xref: delta_avge_mass "958.9113"
-xref: delta_composition "dHex(1) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_959_mono_mass "958.375399"
-xref: spec_1_neutral_loss_959_avge_mass "958.9113"
-xref: spec_1_neutral_loss_959_flag "false"
-xref: spec_1_neutral_loss_959_composition "dHex(1) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_959_mono_mass "958.375399"
-xref: spec_1_neutral_loss_959_avge_mass "958.9113"
-xref: spec_1_neutral_loss_959_flag "false"
-xref: spec_1_neutral_loss_959_composition "dHex(1) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1617
-name: Hex(1)HexNAc(1)NeuAc(1)NeuGc(1)
-def: "Hex HexNAc NeuAc NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=1&neuac=1&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1617]
-xref: record_id "1617"
-xref: delta_mono_mass "963.317944"
-xref: delta_avge_mass "963.8417"
-xref: delta_composition "Hex(1) HexNAc(1) NeuAc(1) NeuGc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_964_mono_mass "963.317944"
-xref: spec_1_neutral_loss_964_avge_mass "963.8417"
-xref: spec_1_neutral_loss_964_flag "false"
-xref: spec_1_neutral_loss_964_composition "Hex(1) HexNAc(1) NeuAc(1) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_964_mono_mass "963.317944"
-xref: spec_1_neutral_loss_964_avge_mass "963.8417"
-xref: spec_1_neutral_loss_964_flag "false"
-xref: spec_1_neutral_loss_964_composition "Hex(1) HexNAc(1) NeuAc(1) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1618
-name: dHex(1)Hex(1)HexNAc(2)Kdn(1)
-def: "DHex Hex HexNAc(2) Kdn ---OR--- Hex(2) HexNAc dHex NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=1&hexnac=2&kdn=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1618]
-xref: record_id "1618"
-xref: delta_mono_mass "964.338345"
-xref: delta_avge_mass "964.8695"
-xref: delta_composition "dHex Hex HexNAc(2) Kdn"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-17 11:43:59"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_965_mono_mass "964.338345"
-xref: spec_1_neutral_loss_965_avge_mass "964.8695"
-xref: spec_1_neutral_loss_965_flag "false"
-xref: spec_1_neutral_loss_965_composition "dHex Hex HexNAc(2) Kdn"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_965_mono_mass "964.338345"
-xref: spec_1_neutral_loss_965_avge_mass "964.8695"
-xref: spec_1_neutral_loss_965_flag "false"
-xref: spec_1_neutral_loss_965_composition "dHex Hex HexNAc(2) Kdn"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1619
-name: Hex(1)HexNAc(1)NeuGc(2)
-def: "Hex HexNAc NeuGc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=1&neugc=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1619]
-xref: record_id "1619"
-xref: delta_mono_mass "979.312859"
-xref: delta_avge_mass "979.8411"
-xref: delta_composition "Hex(1) HexNAc(1) NeuGc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_980_mono_mass "979.312859"
-xref: spec_1_neutral_loss_980_avge_mass "979.8411"
-xref: spec_1_neutral_loss_980_flag "false"
-xref: spec_1_neutral_loss_980_composition "Hex(1) HexNAc(1) NeuGc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_980_mono_mass "979.312859"
-xref: spec_1_neutral_loss_980_avge_mass "979.8411"
-xref: spec_1_neutral_loss_980_flag "false"
-xref: spec_1_neutral_loss_980_composition "Hex(1) HexNAc(1) NeuGc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1620
-name: Hex(1)HexNAc(1)NeuAc(2)Ac(1)
-def: "Ac Hex HexNAc NeuAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?acetyl=1&hex=1&hexnac=1&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1620]
-xref: record_id "1620"
-xref: delta_mono_mass "989.333594"
-xref: delta_avge_mass "989.879"
-xref: delta_composition "Ac Hex HexNAc NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:37:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_990_mono_mass "989.333594"
-xref: spec_1_neutral_loss_990_avge_mass "989.879"
-xref: spec_1_neutral_loss_990_flag "false"
-xref: spec_1_neutral_loss_990_composition "Ac Hex HexNAc NeuAc(2)"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_990_mono_mass "989.333594"
-xref: spec_1_neutral_loss_990_avge_mass "989.879"
-xref: spec_1_neutral_loss_990_flag "false"
-xref: spec_1_neutral_loss_990_composition "Ac Hex HexNAc NeuAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1621
-name: dHex(2)Hex(2)HexA(1)HexNAc(1)
-def: "DHex(2) Hex(2) HexA HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=2&hexa=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1621]
-xref: record_id "1621"
-xref: delta_mono_mass "995.332925"
-xref: delta_avge_mass "995.8802"
-xref: delta_composition "dHex(2) Hex(2) HexA(1) HexNAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_996_mono_mass "995.332925"
-xref: spec_1_neutral_loss_996_avge_mass "995.8802"
-xref: spec_1_neutral_loss_996_flag "false"
-xref: spec_1_neutral_loss_996_composition "dHex(2) Hex(2) HexA(1) HexNAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_996_mono_mass "995.332925"
-xref: spec_1_neutral_loss_996_avge_mass "995.8802"
-xref: spec_1_neutral_loss_996_flag "false"
-xref: spec_1_neutral_loss_996_composition "dHex(2) Hex(2) HexA(1) HexNAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1622
-name: dHex(1)Hex(1)HexNAc(3)Sulf(1)
-def: "DHex Hex HexNAc(3) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=1&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1622]
-xref: record_id "1622"
-xref: delta_mono_mass "997.305665"
-xref: delta_avge_mass "997.9226"
-xref: delta_composition "O(3) S dHex Hex HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:29:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_998_mono_mass "997.305665"
-xref: spec_1_neutral_loss_998_avge_mass "997.9226"
-xref: spec_1_neutral_loss_998_flag "false"
-xref: spec_1_neutral_loss_998_composition "O(3) S dHex Hex HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_998_mono_mass "997.305665"
-xref: spec_1_neutral_loss_998_avge_mass "997.9226"
-xref: spec_1_neutral_loss_998_flag "false"
-xref: spec_1_neutral_loss_998_composition "O(3) S dHex Hex HexNAc(3)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1623
-name: Hex(2)HexA(1)NeuAc(1)Pent(1)Sulf(1)
-def: "Hex(2) HexA NeuAc Pent Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&pent=1&hex=2&hexa=1&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1623]
-xref: record_id "1623"
-xref: delta_mono_mass "1003.232225"
-xref: delta_avge_mass "1003.8377"
-xref: delta_composition "O(3) S Pent Hex(2) HexA NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:29:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1004_mono_mass "1003.232225"
-xref: spec_1_neutral_loss_1004_avge_mass "1003.8377"
-xref: spec_1_neutral_loss_1004_flag "false"
-xref: spec_1_neutral_loss_1004_composition "O(3) S Pent Hex(2) HexA NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1004_mono_mass "1003.232225"
-xref: spec_1_neutral_loss_1004_avge_mass "1003.8377"
-xref: spec_1_neutral_loss_1004_flag "false"
-xref: spec_1_neutral_loss_1004_composition "O(3) S Pent Hex(2) HexA NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1624
-name: dHex(1)Hex(1)HexNAc(2)NeuAc(1)
-def: "DHex Hex HexNAc(2) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=1&hexnac=2&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1624]
-xref: record_id "1624"
-xref: delta_mono_mass "1005.364894"
-xref: delta_avge_mass "1005.9214"
-xref: delta_composition "dHex(1) Hex(1) HexNAc(2) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1006_mono_mass "1005.364894"
-xref: spec_1_neutral_loss_1006_avge_mass "1005.9214"
-xref: spec_1_neutral_loss_1006_flag "false"
-xref: spec_1_neutral_loss_1006_composition "dHex(1) Hex(1) HexNAc(2) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1006_mono_mass "1005.364894"
-xref: spec_1_neutral_loss_1006_avge_mass "1005.9214"
-xref: spec_1_neutral_loss_1006_flag "false"
-xref: spec_1_neutral_loss_1006_composition "dHex(1) Hex(1) HexNAc(2) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1625
-name: dHex(1)Hex(3)HexA(1)HexNAc(1)
-def: "DHex Hex(3) HexA HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexa=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1625]
-xref: record_id "1625"
-xref: delta_mono_mass "1011.32784"
-xref: delta_avge_mass "1011.8796"
-xref: delta_composition "dHex(1) Hex(3) HexA(1) HexNAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1012_mono_mass "1011.32784"
-xref: spec_1_neutral_loss_1012_avge_mass "1011.8796"
-xref: spec_1_neutral_loss_1012_flag "false"
-xref: spec_1_neutral_loss_1012_composition "dHex(1) Hex(3) HexA(1) HexNAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1012_mono_mass "1011.32784"
-xref: spec_1_neutral_loss_1012_avge_mass "1011.8796"
-xref: spec_1_neutral_loss_1012_flag "false"
-xref: spec_1_neutral_loss_1012_composition "dHex(1) Hex(3) HexA(1) HexNAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1626
-name: Hex(2)HexNAc(3)Sulf(1)
-def: "Hex(2) HexNAc(3) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=2&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1626]
-xref: record_id "1626"
-xref: delta_mono_mass "1013.300579"
-xref: delta_avge_mass "1013.922"
-xref: delta_composition "O(3) S Hex(2) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:30:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1014_mono_mass "1013.300579"
-xref: spec_1_neutral_loss_1014_avge_mass "1013.922"
-xref: spec_1_neutral_loss_1014_flag "false"
-xref: spec_1_neutral_loss_1014_composition "O(3) S Hex(2) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1014_mono_mass "1013.300579"
-xref: spec_1_neutral_loss_1014_avge_mass "1013.922"
-xref: spec_1_neutral_loss_1014_flag "false"
-xref: spec_1_neutral_loss_1014_composition "O(3) S Hex(2) HexNAc(3)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1627
-name: Hex(5)HexNAc(1)
-def: "Hex(5) HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=5&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1627]
-xref: record_id "1627"
-xref: delta_mono_mass "1013.34349"
-xref: delta_avge_mass "1013.8955"
-xref: delta_composition "Hex(5) HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-24 11:00:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1014_mono_mass "1013.34349"
-xref: spec_1_neutral_loss_1014_avge_mass "1013.8955"
-xref: spec_1_neutral_loss_1014_flag "false"
-xref: spec_1_neutral_loss_1014_composition "Hex(5) HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1014_mono_mass "1013.34349"
-xref: spec_1_neutral_loss_1014_avge_mass "1013.8955"
-xref: spec_1_neutral_loss_1014_flag "false"
-xref: spec_1_neutral_loss_1014_composition "Hex(5) HexNAc"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1014_mono_mass "1013.34349"
-xref: spec_2_neutral_loss_1014_avge_mass "1013.8955"
-xref: spec_2_neutral_loss_1014_flag "false"
-xref: spec_2_neutral_loss_1014_composition "Hex(5) HexNAc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1628
-name: HexNAc(5)
-def: "HexNAc(5)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1628]
-xref: record_id "1628"
-xref: delta_mono_mass "1015.396863"
-xref: delta_avge_mass "1015.9626"
-xref: delta_composition "HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1016_mono_mass "1015.396863"
-xref: spec_1_neutral_loss_1016_avge_mass "1015.9626"
-xref: spec_1_neutral_loss_1016_flag "false"
-xref: spec_1_neutral_loss_1016_composition "HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1016_mono_mass "1015.396863"
-xref: spec_1_neutral_loss_1016_avge_mass "1015.9626"
-xref: spec_1_neutral_loss_1016_flag "false"
-xref: spec_1_neutral_loss_1016_composition "HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1630
-name: Hex(1)HexNAc(1)NeuAc(2)Ac(2)
-def: "Ac(2) Hex HexNAc NeuAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?acetyl=2&hex=1&hexnac=1&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1630]
-xref: record_id "1630"
-xref: delta_mono_mass "1031.344159"
-xref: delta_avge_mass "1031.9156"
-xref: delta_composition "Ac(2) Hex HexNAc NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:38:10"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1032_mono_mass "1031.344159"
-xref: spec_1_neutral_loss_1032_avge_mass "1031.9156"
-xref: spec_1_neutral_loss_1032_flag "false"
-xref: spec_1_neutral_loss_1032_composition "Ac(2) Hex HexNAc NeuAc(2)"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1032_mono_mass "1031.344159"
-xref: spec_1_neutral_loss_1032_avge_mass "1031.9156"
-xref: spec_1_neutral_loss_1032_flag "false"
-xref: spec_1_neutral_loss_1032_composition "Ac(2) Hex HexNAc NeuAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1631
-name: Hex(2)HexNAc(2)NeuGc(1)
-def: "Hex(2) HexNAc(2) NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=2&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1631]
-xref: record_id "1631"
-xref: delta_mono_mass "1037.354723"
-xref: delta_avge_mass "1037.9202"
-xref: delta_composition "Hex(2) HexNAc(2) NeuGc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1038_mono_mass "1037.354723"
-xref: spec_1_neutral_loss_1038_avge_mass "1037.9202"
-xref: spec_1_neutral_loss_1038_flag "false"
-xref: spec_1_neutral_loss_1038_composition "Hex(2) HexNAc(2) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1038_mono_mass "1037.354723"
-xref: spec_1_neutral_loss_1038_avge_mass "1037.9202"
-xref: spec_1_neutral_loss_1038_flag "false"
-xref: spec_1_neutral_loss_1038_composition "Hex(2) HexNAc(2) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1632
-name: Hex(5)Phos(3)
-def: "Hex(5) Phos(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=3&hex=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1632]
-xref: record_id "1632"
-xref: delta_mono_mass "1050.16311"
-xref: delta_avge_mass "1050.6427"
-xref: delta_composition "H(3) O(9) P(3) Hex(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:42:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1051_mono_mass "1050.16311"
-xref: spec_1_neutral_loss_1051_avge_mass "1050.6427"
-xref: spec_1_neutral_loss_1051_flag "false"
-xref: spec_1_neutral_loss_1051_composition "H(3) O(9) P(3) Hex(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1051_mono_mass "1050.16311"
-xref: spec_1_neutral_loss_1051_avge_mass "1050.6427"
-xref: spec_1_neutral_loss_1051_flag "false"
-xref: spec_1_neutral_loss_1051_composition "H(3) O(9) P(3) Hex(5)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1633
-name: Hex(6)Phos(1)
-def: "Hex(6) Phos." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=1&hex=6&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1633]
-xref: record_id "1633"
-xref: delta_mono_mass "1052.283272"
-xref: delta_avge_mass "1052.8235"
-xref: delta_composition "H O(3) P Hex(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:42:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1053_mono_mass "1052.283272"
-xref: spec_1_neutral_loss_1053_avge_mass "1052.8235"
-xref: spec_1_neutral_loss_1053_flag "false"
-xref: spec_1_neutral_loss_1053_composition "H O(3) P Hex(6)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1053_mono_mass "1052.283272"
-xref: spec_1_neutral_loss_1053_avge_mass "1052.8235"
-xref: spec_1_neutral_loss_1053_flag "false"
-xref: spec_1_neutral_loss_1053_composition "H O(3) P Hex(6)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1634
-name: dHex(1)Hex(2)HexA(1)HexNAc(2)
-def: "DHex Hex(2) HexA HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=2&hexa=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1634]
-xref: record_id "1634"
-xref: delta_mono_mass "1052.354389"
-xref: delta_avge_mass "1052.9316"
-xref: delta_composition "dHex(1) Hex(2) HexA(1) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1053_mono_mass "1052.354389"
-xref: spec_1_neutral_loss_1053_avge_mass "1052.9316"
-xref: spec_1_neutral_loss_1053_flag "false"
-xref: spec_1_neutral_loss_1053_composition "dHex(1) Hex(2) HexA(1) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1053_mono_mass "1052.354389"
-xref: spec_1_neutral_loss_1053_avge_mass "1052.9316"
-xref: spec_1_neutral_loss_1053_flag "false"
-xref: spec_1_neutral_loss_1053_composition "dHex(1) Hex(2) HexA(1) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1635
-name: dHex(2)Hex(3)HexNAc(1)Sulf(1)
-def: "DHex(2) Hex(3) HexNAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=2&hex=3&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1635]
-xref: record_id "1635"
-xref: delta_mono_mass "1061.310475"
-xref: delta_avge_mass "1061.9599"
-xref: delta_composition "O(3) S dHex(2) Hex(3) HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:30:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1062_mono_mass "1061.310475"
-xref: spec_1_neutral_loss_1062_avge_mass "1061.9599"
-xref: spec_1_neutral_loss_1062_flag "false"
-xref: spec_1_neutral_loss_1062_composition "O(3) S dHex(2) Hex(3) HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1062_mono_mass "1061.310475"
-xref: spec_1_neutral_loss_1062_avge_mass "1061.9599"
-xref: spec_1_neutral_loss_1062_flag "false"
-xref: spec_1_neutral_loss_1062_composition "O(3) S dHex(2) Hex(3) HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1636
-name: Hex(1)HexNAc(3)NeuAc(1)
-def: "Hex HexNAc(3) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=3&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1636]
-xref: record_id "1636"
-xref: delta_mono_mass "1062.386358"
-xref: delta_avge_mass "1062.9727"
-xref: delta_composition "Hex(1) HexNAc(3) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1063_mono_mass "1062.386358"
-xref: spec_1_neutral_loss_1063_avge_mass "1062.9727"
-xref: spec_1_neutral_loss_1063_flag "false"
-xref: spec_1_neutral_loss_1063_composition "Hex(1) HexNAc(3) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1063_mono_mass "1062.386358"
-xref: spec_1_neutral_loss_1063_avge_mass "1062.9727"
-xref: spec_1_neutral_loss_1063_flag "false"
-xref: spec_1_neutral_loss_1063_composition "Hex(1) HexNAc(3) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1637
-name: dHex(2)Hex(1)HexNAc(3)
-def: "DHex(2) Hex HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=1&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1637]
-xref: record_id "1637"
-xref: delta_mono_mass "1063.406759"
-xref: delta_avge_mass "1064.0006"
-xref: delta_composition "dHex(2) Hex(1) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1064_mono_mass "1063.406759"
-xref: spec_1_neutral_loss_1064_avge_mass "1064.0006"
-xref: spec_1_neutral_loss_1064_flag "false"
-xref: spec_1_neutral_loss_1064_composition "dHex(2) Hex(1) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1064_mono_mass "1063.406759"
-xref: spec_1_neutral_loss_1064_avge_mass "1064.0006"
-xref: spec_1_neutral_loss_1064_flag "false"
-xref: spec_1_neutral_loss_1064_composition "dHex(2) Hex(1) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1638
-name: Hex(1)HexNAc(3)NeuGc(1)
-def: "Hex HexNAc(3) NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=3&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1638]
-xref: record_id "1638"
-xref: delta_mono_mass "1078.381273"
-xref: delta_avge_mass "1078.9721"
-xref: delta_composition "Hex(1) HexNAc(3) NeuGc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1079_mono_mass "1078.381273"
-xref: spec_1_neutral_loss_1079_avge_mass "1078.9721"
-xref: spec_1_neutral_loss_1079_flag "false"
-xref: spec_1_neutral_loss_1079_composition "Hex(1) HexNAc(3) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1079_mono_mass "1078.381273"
-xref: spec_1_neutral_loss_1079_avge_mass "1078.9721"
-xref: spec_1_neutral_loss_1079_flag "false"
-xref: spec_1_neutral_loss_1079_composition "Hex(1) HexNAc(3) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1639
-name: dHex(1)Hex(1)HexNAc(2)NeuAc(1)Sulf(1)
-def: "DHex Hex HexNAc(2) NeuAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=1&hexnac=2&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1639]
-xref: record_id "1639"
-xref: delta_mono_mass "1085.321709"
-xref: delta_avge_mass "1085.9846"
-xref: delta_composition "O(3) S dHex Hex HexNAc(2) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:30:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1086_mono_mass "1085.321709"
-xref: spec_1_neutral_loss_1086_avge_mass "1085.9846"
-xref: spec_1_neutral_loss_1086_flag "false"
-xref: spec_1_neutral_loss_1086_composition "O(3) S dHex Hex HexNAc(2) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1086_mono_mass "1085.321709"
-xref: spec_1_neutral_loss_1086_avge_mass "1085.9846"
-xref: spec_1_neutral_loss_1086_flag "false"
-xref: spec_1_neutral_loss_1086_composition "O(3) S dHex Hex HexNAc(2) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1640
-name: dHex(1)Hex(3)HexA(1)HexNAc(1)Sulf(1)
-def: "DHex Hex(3) HexA HexNAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=3&hexa=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1640]
-xref: record_id "1640"
-xref: delta_mono_mass "1091.284655"
-xref: delta_avge_mass "1091.9428"
-xref: delta_composition "O(3) S dHex Hex(3) HexA HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:30:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1092_mono_mass "1091.284655"
-xref: spec_1_neutral_loss_1092_avge_mass "1091.9428"
-xref: spec_1_neutral_loss_1092_flag "false"
-xref: spec_1_neutral_loss_1092_composition "O(3) S dHex Hex(3) HexA HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1092_mono_mass "1091.284655"
-xref: spec_1_neutral_loss_1092_avge_mass "1091.9428"
-xref: spec_1_neutral_loss_1092_flag "false"
-xref: spec_1_neutral_loss_1092_composition "O(3) S dHex Hex(3) HexA HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1641
-name: dHex(1)Hex(1)HexA(1)HexNAc(3)
-def: "DHex Hex HexA HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=1&hexa=1&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1641]
-xref: record_id "1641"
-xref: delta_mono_mass "1093.380938"
-xref: delta_avge_mass "1093.9835"
-xref: delta_composition "dHex(1) Hex(1) HexA(1) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1094_mono_mass "1093.380938"
-xref: spec_1_neutral_loss_1094_avge_mass "1093.9835"
-xref: spec_1_neutral_loss_1094_flag "false"
-xref: spec_1_neutral_loss_1094_composition "dHex(1) Hex(1) HexA(1) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1094_mono_mass "1093.380938"
-xref: spec_1_neutral_loss_1094_avge_mass "1093.9835"
-xref: spec_1_neutral_loss_1094_flag "false"
-xref: spec_1_neutral_loss_1094_composition "dHex(1) Hex(1) HexA(1) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1642
-name: Hex(2)HexNAc(2)NeuAc(1)Sulf(1)
-def: "Hex(2) HexNAc(2) NeuAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=2&hexnac=2&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1642]
-xref: record_id "1642"
-xref: delta_mono_mass "1101.316623"
-xref: delta_avge_mass "1101.984"
-xref: delta_composition "O(3) S Hex(2) HexNAc(2) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:30:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1102_mono_mass "1101.316623"
-xref: spec_1_neutral_loss_1102_avge_mass "1101.984"
-xref: spec_1_neutral_loss_1102_flag "false"
-xref: spec_1_neutral_loss_1102_composition "O(3) S Hex(2) HexNAc(2) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1102_mono_mass "1101.316623"
-xref: spec_1_neutral_loss_1102_avge_mass "1101.984"
-xref: spec_1_neutral_loss_1102_flag "false"
-xref: spec_1_neutral_loss_1102_composition "O(3) S Hex(2) HexNAc(2) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1643
-name: dHex(2)Hex(2)HexNAc(2)Sulf(1)
-def: "DHex(2) Hex(2) HexNAc(2) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=2&hex=2&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1643]
-xref: record_id "1643"
-xref: delta_mono_mass "1102.337025"
-xref: delta_avge_mass "1103.0118"
-xref: delta_composition "O(3) S dHex(2) Hex(2) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:31:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1103_mono_mass "1102.337025"
-xref: spec_1_neutral_loss_1103_avge_mass "1103.0118"
-xref: spec_1_neutral_loss_1103_flag "false"
-xref: spec_1_neutral_loss_1103_composition "O(3) S dHex(2) Hex(2) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1103_mono_mass "1102.337025"
-xref: spec_1_neutral_loss_1103_avge_mass "1103.0118"
-xref: spec_1_neutral_loss_1103_flag "false"
-xref: spec_1_neutral_loss_1103_composition "O(3) S dHex(2) Hex(2) HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1644
-name: dHex(2)Hex(1)HexNAc(2)Kdn(1)
-def: "DHex(2) Hex HexNAc(2) Kdn ---OR--- Hex(2) HexNAc dHex(2) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=1&hexnac=2&kdn=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1644]
-xref: record_id "1644"
-xref: delta_mono_mass "1110.396254"
-xref: delta_avge_mass "1111.0107"
-xref: delta_composition "dHex(2) Hex HexNAc(2) Kdn"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-17 12:14:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1111_mono_mass "1110.396254"
-xref: spec_1_neutral_loss_1111_avge_mass "1111.0107"
-xref: spec_1_neutral_loss_1111_flag "false"
-xref: spec_1_neutral_loss_1111_composition "dHex(2) Hex HexNAc(2) Kdn"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1111_mono_mass "1110.396254"
-xref: spec_1_neutral_loss_1111_avge_mass "1111.0107"
-xref: spec_1_neutral_loss_1111_flag "false"
-xref: spec_1_neutral_loss_1111_composition "dHex(2) Hex HexNAc(2) Kdn"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1645
-name: dHex(1)Hex(1)HexNAc(4)
-def: "DHex Hex HexNAc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=1&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1645]
-xref: record_id "1645"
-xref: delta_mono_mass "1120.428223"
-xref: delta_avge_mass "1121.0519"
-xref: delta_composition "dHex(1) Hex(1) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1121_mono_mass "1120.428223"
-xref: spec_1_neutral_loss_1121_avge_mass "1121.0519"
-xref: spec_1_neutral_loss_1121_flag "false"
-xref: spec_1_neutral_loss_1121_composition "dHex(1) Hex(1) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1121_mono_mass "1120.428223"
-xref: spec_1_neutral_loss_1121_avge_mass "1121.0519"
-xref: spec_1_neutral_loss_1121_flag "false"
-xref: spec_1_neutral_loss_1121_composition "dHex(1) Hex(1) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1646
-name: Hex(2)HexNAc(4)
-def: "Hex(2) HexNAc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1646]
-xref: record_id "1646"
-xref: delta_mono_mass "1136.423137"
-xref: delta_avge_mass "1137.0513"
-xref: delta_composition "Hex(2) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-24 11:06:46"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1137_mono_mass "1136.423137"
-xref: spec_1_neutral_loss_1137_avge_mass "1137.0513"
-xref: spec_1_neutral_loss_1137_flag "false"
-xref: spec_1_neutral_loss_1137_composition "Hex(2) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1137_mono_mass "1136.423137"
-xref: spec_1_neutral_loss_1137_avge_mass "1137.0513"
-xref: spec_1_neutral_loss_1137_flag "false"
-xref: spec_1_neutral_loss_1137_composition "Hex(2) HexNAc(4)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1137_mono_mass "1136.423137"
-xref: spec_2_neutral_loss_1137_avge_mass "1137.0513"
-xref: spec_2_neutral_loss_1137_flag "false"
-xref: spec_2_neutral_loss_1137_composition "Hex(2) HexNAc(4)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1647
-name: Hex(2)HexNAc(1)NeuGc(2)
-def: "Hex(2) HexNAc NeuGc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=1&neugc=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1647]
-xref: record_id "1647"
-xref: delta_mono_mass "1141.365682"
-xref: delta_avge_mass "1141.9817"
-xref: delta_composition "Hex(2) HexNAc(1) NeuGc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1142_mono_mass "1141.365682"
-xref: spec_1_neutral_loss_1142_avge_mass "1141.9817"
-xref: spec_1_neutral_loss_1142_flag "false"
-xref: spec_1_neutral_loss_1142_composition "Hex(2) HexNAc(1) NeuGc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1142_mono_mass "1141.365682"
-xref: spec_1_neutral_loss_1142_avge_mass "1141.9817"
-xref: spec_1_neutral_loss_1142_flag "false"
-xref: spec_1_neutral_loss_1142_composition "Hex(2) HexNAc(1) NeuGc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1648
-name: dHex(2)Hex(4)HexNAc(1)
-def: "DHex(2) Hex(4) HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=4&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1648]
-xref: record_id "1648"
-xref: delta_mono_mass "1143.406484"
-xref: delta_avge_mass "1144.0373"
-xref: delta_composition "dHex(2) Hex(4) HexNAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1144_mono_mass "1143.406484"
-xref: spec_1_neutral_loss_1144_avge_mass "1144.0373"
-xref: spec_1_neutral_loss_1144_flag "false"
-xref: spec_1_neutral_loss_1144_composition "dHex(2) Hex(4) HexNAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1144_mono_mass "1143.406484"
-xref: spec_1_neutral_loss_1144_avge_mass "1144.0373"
-xref: spec_1_neutral_loss_1144_flag "false"
-xref: spec_1_neutral_loss_1144_composition "dHex(2) Hex(4) HexNAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1649
-name: Hex(1)HexNAc(2)NeuAc(2)
-def: "Hex HexNAc(2) NeuAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=2&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1649]
-xref: record_id "1649"
-xref: delta_mono_mass "1150.402402"
-xref: delta_avge_mass "1151.0348"
-xref: delta_composition "Hex(1) HexNAc(2) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1151_mono_mass "1150.402402"
-xref: spec_1_neutral_loss_1151_avge_mass "1151.0348"
-xref: spec_1_neutral_loss_1151_flag "false"
-xref: spec_1_neutral_loss_1151_composition "Hex(1) HexNAc(2) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1151_mono_mass "1150.402402"
-xref: spec_1_neutral_loss_1151_avge_mass "1151.0348"
-xref: spec_1_neutral_loss_1151_flag "false"
-xref: spec_1_neutral_loss_1151_composition "Hex(1) HexNAc(2) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1650
-name: dHex(2)Hex(1)HexNAc(2)NeuAc(1)
-def: "DHex(2) Hex HexNAc(2) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=1&hexnac=2&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1650]
-xref: record_id "1650"
-xref: delta_mono_mass "1151.422803"
-xref: delta_avge_mass "1152.0626"
-xref: delta_composition "dHex(2) Hex(1) HexNAc(2) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1152_mono_mass "1151.422803"
-xref: spec_1_neutral_loss_1152_avge_mass "1152.0626"
-xref: spec_1_neutral_loss_1152_flag "false"
-xref: spec_1_neutral_loss_1152_composition "dHex(2) Hex(1) HexNAc(2) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1152_mono_mass "1151.422803"
-xref: spec_1_neutral_loss_1152_avge_mass "1152.0626"
-xref: spec_1_neutral_loss_1152_flag "false"
-xref: spec_1_neutral_loss_1152_composition "dHex(2) Hex(1) HexNAc(2) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1651
-name: dHex(1)Hex(2)HexNAc(3)Sulf(1)
-def: "DHex Hex(2) HexNAc(3) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=2&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1651]
-xref: record_id "1651"
-xref: delta_mono_mass "1159.358488"
-xref: delta_avge_mass "1160.0632"
-xref: delta_composition "O(3) S dHex Hex(2) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:31:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1160_mono_mass "1159.358488"
-xref: spec_1_neutral_loss_1160_avge_mass "1160.0632"
-xref: spec_1_neutral_loss_1160_flag "false"
-xref: spec_1_neutral_loss_1160_composition "O(3) S dHex Hex(2) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1160_mono_mass "1159.358488"
-xref: spec_1_neutral_loss_1160_avge_mass "1160.0632"
-xref: spec_1_neutral_loss_1160_flag "false"
-xref: spec_1_neutral_loss_1160_composition "O(3) S dHex Hex(2) HexNAc(3)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1652
-name: dHex(1)HexNAc(5)
-def: "DHex HexNAc(5)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1652]
-xref: record_id "1652"
-xref: delta_mono_mass "1161.454772"
-xref: delta_avge_mass "1162.1038"
-xref: delta_composition "dHex(1) HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1162_mono_mass "1161.454772"
-xref: spec_1_neutral_loss_1162_avge_mass "1162.1038"
-xref: spec_1_neutral_loss_1162_flag "false"
-xref: spec_1_neutral_loss_1162_composition "dHex(1) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1162_mono_mass "1161.454772"
-xref: spec_1_neutral_loss_1162_avge_mass "1162.1038"
-xref: spec_1_neutral_loss_1162_flag "false"
-xref: spec_1_neutral_loss_1162_composition "dHex(1) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1653
-name: dHex(2)Hex(1)HexNAc(2)NeuGc(1)
-def: "DHex(2) Hex HexNAc(2) NeuGc ---OR--- Hex(2) HexNAc(2) dHex NeuAc ---OR--- Hex HexNAc(3) dHex Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=1&hexnac=2&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1653]
-xref: record_id "1653"
-xref: delta_mono_mass "1167.417718"
-xref: delta_avge_mass "1168.062"
-xref: delta_composition "dHex(2) Hex HexNAc(2) NeuGc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-17 12:18:14"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1168_mono_mass "1167.417718"
-xref: spec_1_neutral_loss_1168_avge_mass "1168.062"
-xref: spec_1_neutral_loss_1168_flag "false"
-xref: spec_1_neutral_loss_1168_composition "dHex(2) Hex HexNAc(2) NeuGc"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1168_mono_mass "1167.417718"
-xref: spec_1_neutral_loss_1168_avge_mass "1168.062"
-xref: spec_1_neutral_loss_1168_flag "false"
-xref: spec_1_neutral_loss_1168_composition "dHex(2) Hex HexNAc(2) NeuGc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1654
-name: dHex(3)Hex(2)HexNAc(2)
-def: "DHex(3) Hex(2) HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=3&hex=2&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1654]
-xref: record_id "1654"
-xref: delta_mono_mass "1168.438119"
-xref: delta_avge_mass "1169.0898"
-xref: delta_composition "dHex(3) Hex(2) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1169_mono_mass "1168.438119"
-xref: spec_1_neutral_loss_1169_avge_mass "1169.0898"
-xref: spec_1_neutral_loss_1169_flag "false"
-xref: spec_1_neutral_loss_1169_composition "dHex(3) Hex(2) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1169_mono_mass "1168.438119"
-xref: spec_1_neutral_loss_1169_avge_mass "1169.0898"
-xref: spec_1_neutral_loss_1169_flag "false"
-xref: spec_1_neutral_loss_1169_composition "dHex(3) Hex(2) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1655
-name: Hex(3)HexNAc(3)Sulf(1)
-def: "Hex(3) HexNAc(3) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=3&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1655]
-xref: record_id "1655"
-xref: delta_mono_mass "1175.353403"
-xref: delta_avge_mass "1176.0626"
-xref: delta_composition "O(3) S Hex(3) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-24 11:08:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1176_mono_mass "1175.353403"
-xref: spec_1_neutral_loss_1176_avge_mass "1176.0626"
-xref: spec_1_neutral_loss_1176_flag "false"
-xref: spec_1_neutral_loss_1176_composition "O(3) S Hex(3) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1176_mono_mass "1175.353403"
-xref: spec_1_neutral_loss_1176_avge_mass "1176.0626"
-xref: spec_1_neutral_loss_1176_flag "false"
-xref: spec_1_neutral_loss_1176_composition "O(3) S Hex(3) HexNAc(3)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1176_mono_mass "1175.353403"
-xref: spec_2_neutral_loss_1176_avge_mass "1176.0626"
-xref: spec_2_neutral_loss_1176_flag "false"
-xref: spec_2_neutral_loss_1176_composition "O(3) S Hex(3) HexNAc(3)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1656
-name: dHex(2)Hex(2)HexNAc(2)Sulf(2)
-def: "DHex(2) Hex(2) HexNAc(2) Sulf(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=2&dhex=2&hex=2&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1656]
-xref: record_id "1656"
-xref: delta_mono_mass "1182.293839"
-xref: delta_avge_mass "1183.075"
-xref: delta_composition "O(6) S(2) dHex(2) Hex(2) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:31:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1183_mono_mass "1182.293839"
-xref: spec_1_neutral_loss_1183_avge_mass "1183.075"
-xref: spec_1_neutral_loss_1183_flag "false"
-xref: spec_1_neutral_loss_1183_composition "O(6) S(2) dHex(2) Hex(2) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1183_mono_mass "1182.293839"
-xref: spec_1_neutral_loss_1183_avge_mass "1183.075"
-xref: spec_1_neutral_loss_1183_flag "false"
-xref: spec_1_neutral_loss_1183_composition "O(6) S(2) dHex(2) Hex(2) HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1657
-name: dHex(1)Hex(2)HexNAc(2)NeuGc(1)
-def: "DHex Hex(2) HexNAc(2) NeuGc ---OR--- Hex(3) HexNAc(2) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=2&hexnac=2&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1657]
-xref: record_id "1657"
-xref: delta_mono_mass "1183.412632"
-xref: delta_avge_mass "1184.0614"
-xref: delta_composition "dHex Hex(2) HexNAc(2) NeuGc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-17 13:10:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1184_mono_mass "1183.412632"
-xref: spec_1_neutral_loss_1184_avge_mass "1184.0614"
-xref: spec_1_neutral_loss_1184_flag "false"
-xref: spec_1_neutral_loss_1184_composition "dHex Hex(2) HexNAc(2) NeuGc"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1184_mono_mass "1183.412632"
-xref: spec_1_neutral_loss_1184_avge_mass "1184.0614"
-xref: spec_1_neutral_loss_1184_flag "false"
-xref: spec_1_neutral_loss_1184_composition "dHex Hex(2) HexNAc(2) NeuGc"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1184_mono_mass "1183.412632"
-xref: spec_2_neutral_loss_1184_avge_mass "1184.0614"
-xref: spec_2_neutral_loss_1184_flag "false"
-xref: spec_2_neutral_loss_1184_composition "dHex Hex(2) HexNAc(2) NeuGc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1658
-name: dHex(1)Hex(1)HexNAc(3)NeuAc(1)
-def: "DHex Hex HexNAc(3) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=1&hexnac=3&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1658]
-xref: record_id "1658"
-xref: delta_mono_mass "1208.444267"
-xref: delta_avge_mass "1209.1139"
-xref: delta_composition "dHex Hex HexNAc(3) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-23 14:50:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1209_mono_mass "1208.444267"
-xref: spec_1_neutral_loss_1209_avge_mass "1209.1139"
-xref: spec_1_neutral_loss_1209_flag "false"
-xref: spec_1_neutral_loss_1209_composition "dHex Hex HexNAc(3) NeuAc"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1209_mono_mass "1208.444267"
-xref: spec_1_neutral_loss_1209_avge_mass "1209.1139"
-xref: spec_1_neutral_loss_1209_flag "false"
-xref: spec_1_neutral_loss_1209_composition "dHex Hex HexNAc(3) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1659
-name: Hex(6)Phos(3)
-def: "Hex(6) Phos(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=3&hex=6&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1659]
-xref: record_id "1659"
-xref: delta_mono_mass "1212.215934"
-xref: delta_avge_mass "1212.7833"
-xref: delta_composition "H(3) O(9) P(3) Hex(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:42:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1213_mono_mass "1212.215934"
-xref: spec_1_neutral_loss_1213_avge_mass "1212.7833"
-xref: spec_1_neutral_loss_1213_flag "false"
-xref: spec_1_neutral_loss_1213_composition "H(3) O(9) P(3) Hex(6)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1213_mono_mass "1212.215934"
-xref: spec_1_neutral_loss_1213_avge_mass "1212.7833"
-xref: spec_1_neutral_loss_1213_flag "false"
-xref: spec_1_neutral_loss_1213_composition "H(3) O(9) P(3) Hex(6)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1660
-name: dHex(1)Hex(3)HexA(1)HexNAc(2)
-def: "DHex Hex(3) HexA HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexa=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1660]
-xref: record_id "1660"
-xref: delta_mono_mass "1214.407213"
-xref: delta_avge_mass "1215.0722"
-xref: delta_composition "dHex(1) Hex(3) HexA(1) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1215_mono_mass "1214.407213"
-xref: spec_1_neutral_loss_1215_avge_mass "1215.0722"
-xref: spec_1_neutral_loss_1215_flag "false"
-xref: spec_1_neutral_loss_1215_composition "dHex(1) Hex(3) HexA(1) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1215_mono_mass "1214.407213"
-xref: spec_1_neutral_loss_1215_avge_mass "1215.0722"
-xref: spec_1_neutral_loss_1215_flag "false"
-xref: spec_1_neutral_loss_1215_composition "dHex(1) Hex(3) HexA(1) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1661
-name: dHex(1)Hex(1)HexNAc(3)NeuGc(1)
-def: "DHex Hex HexNAc(3) NeuGc ---OR--- Hex(2) HexNAc(3) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=1&hexnac=3&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1661]
-xref: record_id "1661"
-xref: delta_mono_mass "1224.439181"
-xref: delta_avge_mass "1225.1133"
-xref: delta_composition "dHex Hex HexNAc(3) NeuGc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-17 13:15:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1225_mono_mass "1224.439181"
-xref: spec_1_neutral_loss_1225_avge_mass "1225.1133"
-xref: spec_1_neutral_loss_1225_flag "false"
-xref: spec_1_neutral_loss_1225_composition "dHex Hex HexNAc(3) NeuGc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1225_mono_mass "1224.439181"
-xref: spec_1_neutral_loss_1225_avge_mass "1225.1133"
-xref: spec_1_neutral_loss_1225_flag "false"
-xref: spec_1_neutral_loss_1225_composition "dHex Hex HexNAc(3) NeuGc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1662
-name: Hex(1)HexNAc(2)NeuAc(2)Sulf(1)
-def: "Hex HexNAc(2) NeuAc(2) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=1&hexnac=2&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1662]
-xref: record_id "1662"
-xref: delta_mono_mass "1230.359217"
-xref: delta_avge_mass "1231.098"
-xref: delta_composition "O(3) S Hex HexNAc(2) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:31:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1231_mono_mass "1230.359217"
-xref: spec_1_neutral_loss_1231_avge_mass "1231.098"
-xref: spec_1_neutral_loss_1231_flag "false"
-xref: spec_1_neutral_loss_1231_composition "O(3) S Hex HexNAc(2) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1231_mono_mass "1230.359217"
-xref: spec_1_neutral_loss_1231_avge_mass "1231.098"
-xref: spec_1_neutral_loss_1231_flag "false"
-xref: spec_1_neutral_loss_1231_composition "O(3) S Hex HexNAc(2) NeuAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1663
-name: dHex(2)Hex(3)HexA(1)HexNAc(1)Sulf(1)
-def: "DHex(2) Hex(3) HexA HexNAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=2&hex=3&hexa=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1663]
-xref: record_id "1663"
-xref: delta_mono_mass "1237.342563"
-xref: delta_avge_mass "1238.084"
-xref: delta_composition "O(3) S dHex(2) Hex(3) HexA HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:32:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1238_mono_mass "1237.342563"
-xref: spec_1_neutral_loss_1238_avge_mass "1238.084"
-xref: spec_1_neutral_loss_1238_flag "false"
-xref: spec_1_neutral_loss_1238_composition "O(3) S dHex(2) Hex(3) HexA HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1238_mono_mass "1237.342563"
-xref: spec_1_neutral_loss_1238_avge_mass "1238.084"
-xref: spec_1_neutral_loss_1238_flag "false"
-xref: spec_1_neutral_loss_1238_composition "O(3) S dHex(2) Hex(3) HexA HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1664
-name: Hex(1)HexNAc(1)NeuAc(3)
-def: "Hex HexNAc NeuAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=1&neuac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1664]
-xref: record_id "1664"
-xref: delta_mono_mass "1238.418446"
-xref: delta_avge_mass "1239.0969"
-xref: delta_composition "Hex(1) HexNAc(1) NeuAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1239_mono_mass "1238.418446"
-xref: spec_1_neutral_loss_1239_avge_mass "1239.0969"
-xref: spec_1_neutral_loss_1239_flag "false"
-xref: spec_1_neutral_loss_1239_composition "Hex(1) HexNAc(1) NeuAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1239_mono_mass "1238.418446"
-xref: spec_1_neutral_loss_1239_avge_mass "1239.0969"
-xref: spec_1_neutral_loss_1239_flag "false"
-xref: spec_1_neutral_loss_1239_composition "Hex(1) HexNAc(1) NeuAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1665
-name: Hex(2)HexNAc(3)NeuGc(1)
-def: "Hex(2) HexNAc(3) NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=3&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1665]
-xref: record_id "1665"
-xref: delta_mono_mass "1240.434096"
-xref: delta_avge_mass "1241.1127"
-xref: delta_composition "Hex(2) HexNAc(3) NeuGc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1241_mono_mass "1240.434096"
-xref: spec_1_neutral_loss_1241_avge_mass "1241.1127"
-xref: spec_1_neutral_loss_1241_flag "false"
-xref: spec_1_neutral_loss_1241_composition "Hex(2) HexNAc(3) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1241_mono_mass "1240.434096"
-xref: spec_1_neutral_loss_1241_avge_mass "1241.1127"
-xref: spec_1_neutral_loss_1241_flag "false"
-xref: spec_1_neutral_loss_1241_composition "Hex(2) HexNAc(3) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1666
-name: dHex(1)Hex(2)HexNAc(2)NeuAc(1)Sulf(1)
-def: "DHex Hex(2) HexNAc(2) NeuAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=2&hexnac=2&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1666]
-xref: record_id "1666"
-xref: delta_mono_mass "1247.374532"
-xref: delta_avge_mass "1248.1252"
-xref: delta_composition "O(3) S dHex Hex(2) HexNAc(2) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:32:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1248_mono_mass "1247.374532"
-xref: spec_1_neutral_loss_1248_avge_mass "1248.1252"
-xref: spec_1_neutral_loss_1248_flag "false"
-xref: spec_1_neutral_loss_1248_composition "O(3) S dHex Hex(2) HexNAc(2) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1248_mono_mass "1247.374532"
-xref: spec_1_neutral_loss_1248_avge_mass "1248.1252"
-xref: spec_1_neutral_loss_1248_flag "false"
-xref: spec_1_neutral_loss_1248_composition "O(3) S dHex Hex(2) HexNAc(2) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1667
-name: dHex(3)Hex(1)HexNAc(2)Kdn(1)
-def: "DHex(3) Hex HexNAc(2) Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=3&hex=1&hexnac=2&kdn=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1667]
-xref: record_id "1667"
-xref: delta_mono_mass "1256.454163"
-xref: delta_avge_mass "1257.1519"
-xref: delta_composition "dHex(3) Hex HexNAc(2) Kdn"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 15:57:10"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1257_mono_mass "1256.454163"
-xref: spec_1_neutral_loss_1257_avge_mass "1257.1519"
-xref: spec_1_neutral_loss_1257_flag "false"
-xref: spec_1_neutral_loss_1257_composition "dHex(3) Hex HexNAc(2) Kdn"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1257_mono_mass "1256.454163"
-xref: spec_1_neutral_loss_1257_avge_mass "1257.1519"
-xref: spec_1_neutral_loss_1257_flag "false"
-xref: spec_1_neutral_loss_1257_composition "dHex(3) Hex HexNAc(2) Kdn"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1668
-name: dHex(2)Hex(3)HexNAc(2)Sulf(1)
-def: "DHex(2) Hex(3) HexNAc(2) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=2&hex=3&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1668]
-xref: record_id "1668"
-xref: delta_mono_mass "1264.389848"
-xref: delta_avge_mass "1265.1524"
-xref: delta_composition "O(3) S dHex(2) Hex(3) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:32:32"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1265_mono_mass "1264.389848"
-xref: spec_1_neutral_loss_1265_avge_mass "1265.1524"
-xref: spec_1_neutral_loss_1265_flag "false"
-xref: spec_1_neutral_loss_1265_composition "O(3) S dHex(2) Hex(3) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1265_mono_mass "1264.389848"
-xref: spec_1_neutral_loss_1265_avge_mass "1265.1524"
-xref: spec_1_neutral_loss_1265_flag "false"
-xref: spec_1_neutral_loss_1265_composition "O(3) S dHex(2) Hex(3) HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1669
-name: dHex(2)Hex(2)HexNAc(2)Kdn(1)
-def: "DHex(2) Hex(2) HexNAc(2) Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=2&hexnac=2&kdn=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1669]
-xref: record_id "1669"
-xref: delta_mono_mass "1272.449077"
-xref: delta_avge_mass "1273.1513"
-xref: delta_composition "dHex(2) Hex(2) HexNAc(2) Kdn"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 15:56:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1273_mono_mass "1272.449077"
-xref: spec_1_neutral_loss_1273_avge_mass "1273.1513"
-xref: spec_1_neutral_loss_1273_flag "false"
-xref: spec_1_neutral_loss_1273_composition "dHex(2) Hex(2) HexNAc(2) Kdn"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1273_mono_mass "1272.449077"
-xref: spec_1_neutral_loss_1273_avge_mass "1273.1513"
-xref: spec_1_neutral_loss_1273_flag "false"
-xref: spec_1_neutral_loss_1273_composition "dHex(2) Hex(2) HexNAc(2) Kdn"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1670
-name: dHex(2)Hex(2)HexA(1)HexNAc(2)Sulf(1)
-def: "DHex(2) Hex(2) HexA HexNAc(2) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=2&hex=2&hexa=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1670]
-xref: record_id "1670"
-xref: delta_mono_mass "1278.369113"
-xref: delta_avge_mass "1279.136"
-xref: delta_composition "O(3) S dHex(2) Hex(2) HexA HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:32:43"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1279_mono_mass "1278.369113"
-xref: spec_1_neutral_loss_1279_avge_mass "1279.136"
-xref: spec_1_neutral_loss_1279_flag "false"
-xref: spec_1_neutral_loss_1279_composition "O(3) S dHex(2) Hex(2) HexA HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1279_mono_mass "1278.369113"
-xref: spec_1_neutral_loss_1279_avge_mass "1279.136"
-xref: spec_1_neutral_loss_1279_flag "false"
-xref: spec_1_neutral_loss_1279_composition "O(3) S dHex(2) Hex(2) HexA HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1671
-name: dHex(1)Hex(2)HexNAc(4)
-def: "DHex Hex(2) HexNAc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=2&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1671]
-xref: record_id "1671"
-xref: delta_mono_mass "1282.481046"
-xref: delta_avge_mass "1283.1925"
-xref: delta_composition "dHex Hex(2) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-24 12:00:46"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1283_mono_mass "1282.481046"
-xref: spec_1_neutral_loss_1283_avge_mass "1283.1925"
-xref: spec_1_neutral_loss_1283_flag "false"
-xref: spec_1_neutral_loss_1283_composition "dHex Hex(2) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1283_mono_mass "1282.481046"
-xref: spec_1_neutral_loss_1283_avge_mass "1283.1925"
-xref: spec_1_neutral_loss_1283_flag "false"
-xref: spec_1_neutral_loss_1283_composition "dHex Hex(2) HexNAc(4)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1283_mono_mass "1282.481046"
-xref: spec_2_neutral_loss_1283_avge_mass "1283.1925"
-xref: spec_2_neutral_loss_1283_flag "false"
-xref: spec_2_neutral_loss_1283_composition "dHex Hex(2) HexNAc(4)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1672
-name: Hex(1)HexNAc(1)NeuGc(3)
-def: "Hex HexNAc NeuGc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=1&neugc=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1672]
-xref: record_id "1672"
-xref: delta_mono_mass "1286.40319"
-xref: delta_avge_mass "1287.0951"
-xref: delta_composition "Hex(1) HexNAc(1) NeuGc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1287_mono_mass "1286.40319"
-xref: spec_1_neutral_loss_1287_avge_mass "1287.0951"
-xref: spec_1_neutral_loss_1287_flag "false"
-xref: spec_1_neutral_loss_1287_composition "Hex(1) HexNAc(1) NeuGc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1287_mono_mass "1286.40319"
-xref: spec_1_neutral_loss_1287_avge_mass "1287.0951"
-xref: spec_1_neutral_loss_1287_flag "false"
-xref: spec_1_neutral_loss_1287_composition "Hex(1) HexNAc(1) NeuGc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1673
-name: dHex(1)Hex(1)HexNAc(3)NeuAc(1)Sulf(1)
-def: "DHex Hex HexNAc(3) NeuAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=1&hexnac=3&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1673]
-xref: record_id "1673"
-xref: delta_mono_mass "1288.401081"
-xref: delta_avge_mass "1289.1771"
-xref: delta_composition "O(3) S dHex Hex HexNAc(3) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:32:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1289_mono_mass "1288.401081"
-xref: spec_1_neutral_loss_1289_avge_mass "1289.1771"
-xref: spec_1_neutral_loss_1289_flag "false"
-xref: spec_1_neutral_loss_1289_composition "O(3) S dHex Hex HexNAc(3) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1289_mono_mass "1288.401081"
-xref: spec_1_neutral_loss_1289_avge_mass "1289.1771"
-xref: spec_1_neutral_loss_1289_flag "false"
-xref: spec_1_neutral_loss_1289_composition "O(3) S dHex Hex HexNAc(3) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1674
-name: dHex(1)Hex(3)HexA(1)HexNAc(2)Sulf(1)
-def: "DHex Hex(3) HexA HexNAc(2) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=3&hexa=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1674]
-xref: record_id "1674"
-xref: delta_mono_mass "1294.364027"
-xref: delta_avge_mass "1295.1354"
-xref: delta_composition "O(3) S dHex Hex(3) HexA HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:33:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1295_mono_mass "1294.364027"
-xref: spec_1_neutral_loss_1295_avge_mass "1295.1354"
-xref: spec_1_neutral_loss_1295_flag "false"
-xref: spec_1_neutral_loss_1295_composition "O(3) S dHex Hex(3) HexA HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1295_mono_mass "1294.364027"
-xref: spec_1_neutral_loss_1295_avge_mass "1295.1354"
-xref: spec_1_neutral_loss_1295_flag "false"
-xref: spec_1_neutral_loss_1295_composition "O(3) S dHex Hex(3) HexA HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1675
-name: dHex(1)Hex(1)HexNAc(2)NeuAc(2)
-def: "DHex Hex HexNAc(2) NeuAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=1&hexnac=2&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1675]
-xref: record_id "1675"
-xref: delta_mono_mass "1296.460311"
-xref: delta_avge_mass "1297.176"
-xref: delta_composition "dHex(1) Hex(1) HexNAc(2) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1297_mono_mass "1296.460311"
-xref: spec_1_neutral_loss_1297_avge_mass "1297.176"
-xref: spec_1_neutral_loss_1297_flag "false"
-xref: spec_1_neutral_loss_1297_composition "dHex(1) Hex(1) HexNAc(2) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1297_mono_mass "1296.460311"
-xref: spec_1_neutral_loss_1297_avge_mass "1297.176"
-xref: spec_1_neutral_loss_1297_flag "false"
-xref: spec_1_neutral_loss_1297_composition "dHex(1) Hex(1) HexNAc(2) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1676
-name: dHex(3)HexNAc(3)Kdn(1)
-def: "DHex(3) HexNAc(3) Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=3&hexnac=3&kdn=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1676]
-xref: record_id "1676"
-xref: delta_mono_mass "1297.480712"
-xref: delta_avge_mass "1298.2038"
-xref: delta_composition "dHex(3) HexNAc(3) Kdn"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 15:57:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1298_mono_mass "1297.480712"
-xref: spec_1_neutral_loss_1298_avge_mass "1298.2038"
-xref: spec_1_neutral_loss_1298_flag "false"
-xref: spec_1_neutral_loss_1298_composition "dHex(3) HexNAc(3) Kdn"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1298_mono_mass "1297.480712"
-xref: spec_1_neutral_loss_1298_avge_mass "1298.2038"
-xref: spec_1_neutral_loss_1298_flag "false"
-xref: spec_1_neutral_loss_1298_composition "dHex(3) HexNAc(3) Kdn"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1678
-name: Hex(2)HexNAc(3)NeuAc(1)Sulf(1)
-def: "Hex(2) HexNAc(3) NeuAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=2&hexnac=3&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1678]
-xref: record_id "1678"
-xref: delta_mono_mass "1304.395996"
-xref: delta_avge_mass "1305.1765"
-xref: delta_composition "O(3) S Hex(2) HexNAc(3) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:33:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1305_mono_mass "1304.395996"
-xref: spec_1_neutral_loss_1305_avge_mass "1305.1765"
-xref: spec_1_neutral_loss_1305_flag "false"
-xref: spec_1_neutral_loss_1305_composition "O(3) S Hex(2) HexNAc(3) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1305_mono_mass "1304.395996"
-xref: spec_1_neutral_loss_1305_avge_mass "1305.1765"
-xref: spec_1_neutral_loss_1305_flag "false"
-xref: spec_1_neutral_loss_1305_composition "O(3) S Hex(2) HexNAc(3) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1679
-name: dHex(2)Hex(2)HexNAc(3)Sulf(1)
-def: "DHex(2) Hex(2) HexNAc(3) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=2&hex=2&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1679]
-xref: record_id "1679"
-xref: delta_mono_mass "1305.416397"
-xref: delta_avge_mass "1306.2044"
-xref: delta_composition "O(3) S dHex(2) Hex(2) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:33:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1306_mono_mass "1305.416397"
-xref: spec_1_neutral_loss_1306_avge_mass "1306.2044"
-xref: spec_1_neutral_loss_1306_flag "false"
-xref: spec_1_neutral_loss_1306_composition "O(3) S dHex(2) Hex(2) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1306_mono_mass "1305.416397"
-xref: spec_1_neutral_loss_1306_avge_mass "1306.2044"
-xref: spec_1_neutral_loss_1306_flag "false"
-xref: spec_1_neutral_loss_1306_composition "O(3) S dHex(2) Hex(2) HexNAc(3)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1680
-name: dHex(2)HexNAc(5)
-def: "DHex(2) HexNAc(5)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1680]
-xref: record_id "1680"
-xref: delta_mono_mass "1307.512681"
-xref: delta_avge_mass "1308.245"
-xref: delta_composition "dHex(2) HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1308_mono_mass "1307.512681"
-xref: spec_1_neutral_loss_1308_avge_mass "1308.245"
-xref: spec_1_neutral_loss_1308_flag "false"
-xref: spec_1_neutral_loss_1308_composition "dHex(2) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1308_mono_mass "1307.512681"
-xref: spec_1_neutral_loss_1308_avge_mass "1308.245"
-xref: spec_1_neutral_loss_1308_flag "false"
-xref: spec_1_neutral_loss_1308_composition "dHex(2) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1681
-name: Hex(2)HexNAc(2)NeuAc(2)
-def: "Hex(2) HexNAc(2) NeuAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=2&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1681]
-xref: record_id "1681"
-xref: delta_mono_mass "1312.455225"
-xref: delta_avge_mass "1313.1754"
-xref: delta_composition "Hex(2) HexNAc(2) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1313_mono_mass "1312.455225"
-xref: spec_1_neutral_loss_1313_avge_mass "1313.1754"
-xref: spec_1_neutral_loss_1313_flag "false"
-xref: spec_1_neutral_loss_1313_composition "Hex(2) HexNAc(2) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1313_mono_mass "1312.455225"
-xref: spec_1_neutral_loss_1313_avge_mass "1313.1754"
-xref: spec_1_neutral_loss_1313_flag "false"
-xref: spec_1_neutral_loss_1313_composition "Hex(2) HexNAc(2) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1682
-name: dHex(2)Hex(2)HexNAc(2)NeuAc(1)
-def: "DHex(2) Hex(2) HexNAc(2) NeuAc ---OR--- Hex HexNAc(3) dHex(2) Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=2&hexnac=2&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1682]
-xref: record_id "1682"
-xref: delta_mono_mass "1313.475627"
-xref: delta_avge_mass "1314.2032"
-xref: delta_composition "dHex(2) Hex(2) HexNAc(2) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-17 13:21:07"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1314_mono_mass "1313.475627"
-xref: spec_1_neutral_loss_1314_avge_mass "1314.2032"
-xref: spec_1_neutral_loss_1314_flag "false"
-xref: spec_1_neutral_loss_1314_composition "dHex(2) Hex(2) HexNAc(2) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1314_mono_mass "1313.475627"
-xref: spec_1_neutral_loss_1314_avge_mass "1314.2032"
-xref: spec_1_neutral_loss_1314_flag "false"
-xref: spec_1_neutral_loss_1314_composition "dHex(2) Hex(2) HexNAc(2) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1683
-name: dHex(1)Hex(3)HexNAc(3)Sulf(1)
-def: "DHex Hex(3) HexNAc(3) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=3&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1683]
-xref: record_id "1683"
-xref: delta_mono_mass "1321.411312"
-xref: delta_avge_mass "1322.2038"
-xref: delta_composition "O(3) S dHex Hex(3) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:33:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1322_mono_mass "1321.411312"
-xref: spec_1_neutral_loss_1322_avge_mass "1322.2038"
-xref: spec_1_neutral_loss_1322_flag "false"
-xref: spec_1_neutral_loss_1322_composition "O(3) S dHex Hex(3) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1322_mono_mass "1321.411312"
-xref: spec_1_neutral_loss_1322_avge_mass "1322.2038"
-xref: spec_1_neutral_loss_1322_flag "false"
-xref: spec_1_neutral_loss_1322_composition "O(3) S dHex Hex(3) HexNAc(3)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1684
-name: dHex(2)Hex(2)HexNAc(2)NeuGc(1)
-def: "DHex(2) Hex(2) HexNAc(2) NeuGc ---OR--- Hex(3) HexNAc(2) dHex NeuAc ---OR--- Hex(2) HexNAc(3) dHex Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=2&hexnac=2&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1684]
-xref: record_id "1684"
-xref: delta_mono_mass "1329.470541"
-xref: delta_avge_mass "1330.2026"
-xref: delta_composition "dHex(2) Hex(2) HexNAc(2) NeuGc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-17 13:27:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1330_mono_mass "1329.470541"
-xref: spec_1_neutral_loss_1330_avge_mass "1330.2026"
-xref: spec_1_neutral_loss_1330_flag "false"
-xref: spec_1_neutral_loss_1330_composition "dHex(2) Hex(2) HexNAc(2) NeuGc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1330_mono_mass "1329.470541"
-xref: spec_1_neutral_loss_1330_avge_mass "1330.2026"
-xref: spec_1_neutral_loss_1330_flag "false"
-xref: spec_1_neutral_loss_1330_composition "dHex(2) Hex(2) HexNAc(2) NeuGc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1685
-name: Hex(2)HexNAc(5)
-def: "Hex(2) HexNAc(5)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1685]
-xref: record_id "1685"
-xref: delta_mono_mass "1339.50251"
-xref: delta_avge_mass "1340.2438"
-xref: delta_composition "Hex(2) HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1340_mono_mass "1339.50251"
-xref: spec_1_neutral_loss_1340_avge_mass "1340.2438"
-xref: spec_1_neutral_loss_1340_flag "false"
-xref: spec_1_neutral_loss_1340_composition "Hex(2) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1340_mono_mass "1339.50251"
-xref: spec_1_neutral_loss_1340_avge_mass "1340.2438"
-xref: spec_1_neutral_loss_1340_flag "false"
-xref: spec_1_neutral_loss_1340_composition "Hex(2) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1686
-name: dHex(1)Hex(3)HexNAc(2)NeuGc(1)
-def: "DHex Hex(3) HexNAc(2) NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexnac=2&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1686]
-xref: record_id "1686"
-xref: delta_mono_mass "1345.465456"
-xref: delta_avge_mass "1346.202"
-xref: delta_composition "dHex(1) Hex(3) HexNAc(2) NeuGc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1346_mono_mass "1345.465456"
-xref: spec_1_neutral_loss_1346_avge_mass "1346.202"
-xref: spec_1_neutral_loss_1346_flag "false"
-xref: spec_1_neutral_loss_1346_composition "dHex(1) Hex(3) HexNAc(2) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1346_mono_mass "1345.465456"
-xref: spec_1_neutral_loss_1346_avge_mass "1346.202"
-xref: spec_1_neutral_loss_1346_flag "false"
-xref: spec_1_neutral_loss_1346_composition "dHex(1) Hex(3) HexNAc(2) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1687
-name: Hex(1)HexNAc(3)NeuAc(2)
-def: "Hex HexNAc(3) NeuAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=3&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1687]
-xref: record_id "1687"
-xref: delta_mono_mass "1353.481775"
-xref: delta_avge_mass "1354.2273"
-xref: delta_composition "Hex(1) HexNAc(3) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1354_mono_mass "1353.481775"
-xref: spec_1_neutral_loss_1354_avge_mass "1354.2273"
-xref: spec_1_neutral_loss_1354_flag "false"
-xref: spec_1_neutral_loss_1354_composition "Hex(1) HexNAc(3) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1354_mono_mass "1353.481775"
-xref: spec_1_neutral_loss_1354_avge_mass "1354.2273"
-xref: spec_1_neutral_loss_1354_flag "false"
-xref: spec_1_neutral_loss_1354_composition "Hex(1) HexNAc(3) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1688
-name: dHex(1)Hex(2)HexNAc(3)NeuAc(1)
-def: "DHex Hex(2) HexNAc(3) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=2&hexnac=3&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1688]
-xref: record_id "1688"
-xref: delta_mono_mass "1370.49709"
-xref: delta_avge_mass "1371.2545"
-xref: delta_composition "dHex(1) Hex(2) HexNAc(3) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1371_mono_mass "1370.49709"
-xref: spec_1_neutral_loss_1371_avge_mass "1371.2545"
-xref: spec_1_neutral_loss_1371_flag "false"
-xref: spec_1_neutral_loss_1371_composition "dHex(1) Hex(2) HexNAc(3) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1371_mono_mass "1370.49709"
-xref: spec_1_neutral_loss_1371_avge_mass "1371.2545"
-xref: spec_1_neutral_loss_1371_flag "false"
-xref: spec_1_neutral_loss_1371_composition "dHex(1) Hex(2) HexNAc(3) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1689
-name: dHex(3)Hex(2)HexNAc(3)
-def: "DHex(3) Hex(2) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=3&hex=2&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1689]
-xref: record_id "1689"
-xref: delta_mono_mass "1371.517491"
-xref: delta_avge_mass "1372.2824"
-xref: delta_composition "dHex(3) Hex(2) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1372_mono_mass "1371.517491"
-xref: spec_1_neutral_loss_1372_avge_mass "1372.2824"
-xref: spec_1_neutral_loss_1372_flag "false"
-xref: spec_1_neutral_loss_1372_composition "dHex(3) Hex(2) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1372_mono_mass "1371.517491"
-xref: spec_1_neutral_loss_1372_avge_mass "1372.2824"
-xref: spec_1_neutral_loss_1372_flag "false"
-xref: spec_1_neutral_loss_1372_composition "dHex(3) Hex(2) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1690
-name: Hex(7)Phos(3)
-def: "Hex(7) Phos(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=3&hex=7&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1690]
-xref: record_id "1690"
-xref: delta_mono_mass "1374.268757"
-xref: delta_avge_mass "1374.9239"
-xref: delta_composition "H(3) O(9) P(3) Hex(7)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:43:14"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1375_mono_mass "1374.268757"
-xref: spec_1_neutral_loss_1375_avge_mass "1374.9239"
-xref: spec_1_neutral_loss_1375_flag "false"
-xref: spec_1_neutral_loss_1375_composition "H(3) O(9) P(3) Hex(7)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1375_mono_mass "1374.268757"
-xref: spec_1_neutral_loss_1375_avge_mass "1374.9239"
-xref: spec_1_neutral_loss_1375_flag "false"
-xref: spec_1_neutral_loss_1375_composition "H(3) O(9) P(3) Hex(7)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1691
-name: dHex(1)Hex(4)HexA(1)HexNAc(2)
-def: "DHex Hex(4) HexA HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=4&hexa=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1691]
-xref: record_id "1691"
-xref: delta_mono_mass "1376.460036"
-xref: delta_avge_mass "1377.2128"
-xref: delta_composition "dHex(1) Hex(4) HexA(1) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1377_mono_mass "1376.460036"
-xref: spec_1_neutral_loss_1377_avge_mass "1377.2128"
-xref: spec_1_neutral_loss_1377_flag "false"
-xref: spec_1_neutral_loss_1377_composition "dHex(1) Hex(4) HexA(1) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1377_mono_mass "1376.460036"
-xref: spec_1_neutral_loss_1377_avge_mass "1377.2128"
-xref: spec_1_neutral_loss_1377_flag "false"
-xref: spec_1_neutral_loss_1377_composition "dHex(1) Hex(4) HexA(1) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1692
-name: Hex(3)HexNAc(3)NeuAc(1)
-def: "Hex(3) HexNAc(3) NeuAc ---OR--- Hex(2) HexNAc(3) dHex NeuGc ---OR--- Hex(2) HexNAc(4) Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=3&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1692]
-xref: record_id "1692"
-xref: delta_mono_mass "1386.492005"
-xref: delta_avge_mass "1387.2539"
-xref: delta_composition "Hex(3) HexNAc(3) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-17 15:15:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1387_mono_mass "1386.492005"
-xref: spec_1_neutral_loss_1387_avge_mass "1387.2539"
-xref: spec_1_neutral_loss_1387_flag "false"
-xref: spec_1_neutral_loss_1387_composition "Hex(3) HexNAc(3) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1387_mono_mass "1386.492005"
-xref: spec_1_neutral_loss_1387_avge_mass "1387.2539"
-xref: spec_1_neutral_loss_1387_flag "false"
-xref: spec_1_neutral_loss_1387_composition "Hex(3) HexNAc(3) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1693
-name: dHex(1)Hex(3)HexA(2)HexNAc(2)
-def: "DHex Hex(3) HexA(2) HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexa=2&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1693]
-xref: record_id "1693"
-xref: delta_mono_mass "1390.439301"
-xref: delta_avge_mass "1391.1963"
-xref: delta_composition "dHex(1) Hex(3) HexA(2) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1391_mono_mass "1390.439301"
-xref: spec_1_neutral_loss_1391_avge_mass "1391.1963"
-xref: spec_1_neutral_loss_1391_flag "false"
-xref: spec_1_neutral_loss_1391_composition "dHex(1) Hex(3) HexA(2) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1391_mono_mass "1390.439301"
-xref: spec_1_neutral_loss_1391_avge_mass "1391.1963"
-xref: spec_1_neutral_loss_1391_flag "false"
-xref: spec_1_neutral_loss_1391_composition "dHex(1) Hex(3) HexA(2) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1694
-name: Hex(2)HexNAc(2)NeuAc(2)Sulf(1)
-def: "Hex(2) HexNAc(2) NeuAc(2) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=2&hexnac=2&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1694]
-xref: record_id "1694"
-xref: delta_mono_mass "1392.41204"
-xref: delta_avge_mass "1393.2386"
-xref: delta_composition "O(3) S Hex(2) HexNAc(2) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:34:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1393_mono_mass "1392.41204"
-xref: spec_1_neutral_loss_1393_avge_mass "1393.2386"
-xref: spec_1_neutral_loss_1393_flag "false"
-xref: spec_1_neutral_loss_1393_composition "O(3) S Hex(2) HexNAc(2) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1393_mono_mass "1392.41204"
-xref: spec_1_neutral_loss_1393_avge_mass "1393.2386"
-xref: spec_1_neutral_loss_1393_flag "false"
-xref: spec_1_neutral_loss_1393_composition "O(3) S Hex(2) HexNAc(2) NeuAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1695
-name: dHex(2)Hex(2)HexNAc(2)NeuAc(1)Sulf(1)
-def: "DHex(2) Hex(2) HexNAc(2) NeuAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=2&hex=2&hexnac=2&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1695]
-xref: record_id "1695"
-xref: delta_mono_mass "1393.432441"
-xref: delta_avge_mass "1394.2664"
-xref: delta_composition "O(3) S dHex(2) Hex(2) HexNAc(2) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:34:15"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1394_mono_mass "1393.432441"
-xref: spec_1_neutral_loss_1394_avge_mass "1394.2664"
-xref: spec_1_neutral_loss_1394_flag "false"
-xref: spec_1_neutral_loss_1394_composition "O(3) S dHex(2) Hex(2) HexNAc(2) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1394_mono_mass "1393.432441"
-xref: spec_1_neutral_loss_1394_avge_mass "1394.2664"
-xref: spec_1_neutral_loss_1394_flag "false"
-xref: spec_1_neutral_loss_1394_composition "O(3) S dHex(2) Hex(2) HexNAc(2) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1696
-name: Hex(3)HexNAc(3)NeuGc(1)
-def: "Hex(3) HexNAc(3) NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=3&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1696]
-xref: record_id "1696"
-xref: delta_mono_mass "1402.48692"
-xref: delta_avge_mass "1403.2533"
-xref: delta_composition "Hex(3) HexNAc(3) NeuGc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1403_mono_mass "1402.48692"
-xref: spec_1_neutral_loss_1403_avge_mass "1403.2533"
-xref: spec_1_neutral_loss_1403_flag "false"
-xref: spec_1_neutral_loss_1403_composition "Hex(3) HexNAc(3) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1403_mono_mass "1402.48692"
-xref: spec_1_neutral_loss_1403_avge_mass "1403.2533"
-xref: spec_1_neutral_loss_1403_flag "false"
-xref: spec_1_neutral_loss_1403_composition "Hex(3) HexNAc(3) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1697
-name: dHex(4)Hex(1)HexNAc(2)Kdn(1)
-def: "DHex(4) Hex HexNAc(2) Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=4&hex=1&hexnac=2&kdn=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1697]
-xref: record_id "1697"
-xref: delta_mono_mass "1402.512072"
-xref: delta_avge_mass "1403.2931"
-xref: delta_composition "dHex(4) Hex HexNAc(2) Kdn"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 15:56:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1403_mono_mass "1402.512072"
-xref: spec_1_neutral_loss_1403_avge_mass "1403.2931"
-xref: spec_1_neutral_loss_1403_flag "false"
-xref: spec_1_neutral_loss_1403_composition "dHex(4) Hex HexNAc(2) Kdn"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1403_mono_mass "1402.512072"
-xref: spec_1_neutral_loss_1403_avge_mass "1403.2931"
-xref: spec_1_neutral_loss_1403_flag "false"
-xref: spec_1_neutral_loss_1403_composition "dHex(4) Hex HexNAc(2) Kdn"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1698
-name: dHex(3)Hex(2)HexNAc(2)Kdn(1)
-def: "DHex(3) Hex(2) HexNAc(2) Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=3&hex=2&hexnac=2&kdn=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1698]
-xref: record_id "1698"
-xref: delta_mono_mass "1418.506986"
-xref: delta_avge_mass "1419.2925"
-xref: delta_composition "dHex(3) Hex(2) HexNAc(2) Kdn"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 15:56:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1419_mono_mass "1418.506986"
-xref: spec_1_neutral_loss_1419_avge_mass "1419.2925"
-xref: spec_1_neutral_loss_1419_flag "false"
-xref: spec_1_neutral_loss_1419_composition "dHex(3) Hex(2) HexNAc(2) Kdn"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1419_mono_mass "1418.506986"
-xref: spec_1_neutral_loss_1419_avge_mass "1419.2925"
-xref: spec_1_neutral_loss_1419_flag "false"
-xref: spec_1_neutral_loss_1419_composition "dHex(3) Hex(2) HexNAc(2) Kdn"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1699
-name: dHex(3)Hex(2)HexA(1)HexNAc(2)Sulf(1)
-def: "DHex(3) Hex(2) HexA HexNAc(2) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=3&hex=2&hexa=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1699]
-xref: record_id "1699"
-xref: delta_mono_mass "1424.427021"
-xref: delta_avge_mass "1425.2772"
-xref: delta_composition "O(3) S dHex(3) Hex(2) HexA HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:55:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1425_mono_mass "1424.427021"
-xref: spec_1_neutral_loss_1425_avge_mass "1425.2772"
-xref: spec_1_neutral_loss_1425_flag "false"
-xref: spec_1_neutral_loss_1425_composition "O(3) S dHex(3) Hex(2) HexA HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1425_mono_mass "1424.427021"
-xref: spec_1_neutral_loss_1425_avge_mass "1425.2772"
-xref: spec_1_neutral_loss_1425_flag "false"
-xref: spec_1_neutral_loss_1425_composition "O(3) S dHex(3) Hex(2) HexA HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1700
-name: Hex(2)HexNAc(4)NeuAc(1)
-def: "Hex(2) HexNAc(4) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=4&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1700]
-xref: record_id "1700"
-xref: delta_mono_mass "1427.518554"
-xref: delta_avge_mass "1428.3059"
-xref: delta_composition "Hex(2) HexNAc(4) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1428_mono_mass "1427.518554"
-xref: spec_1_neutral_loss_1428_avge_mass "1428.3059"
-xref: spec_1_neutral_loss_1428_flag "false"
-xref: spec_1_neutral_loss_1428_composition "Hex(2) HexNAc(4) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1428_mono_mass "1427.518554"
-xref: spec_1_neutral_loss_1428_avge_mass "1428.3059"
-xref: spec_1_neutral_loss_1428_flag "false"
-xref: spec_1_neutral_loss_1428_composition "Hex(2) HexNAc(4) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1701
-name: dHex(2)Hex(2)HexNAc(4)
-def: "DHex(2) Hex(2) HexNAc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=2&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1701]
-xref: record_id "1701"
-xref: delta_mono_mass "1428.538955"
-xref: delta_avge_mass "1429.3337"
-xref: delta_composition "dHex(2) Hex(2) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1429_mono_mass "1428.538955"
-xref: spec_1_neutral_loss_1429_avge_mass "1429.3337"
-xref: spec_1_neutral_loss_1429_flag "false"
-xref: spec_1_neutral_loss_1429_composition "dHex(2) Hex(2) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1429_mono_mass "1428.538955"
-xref: spec_1_neutral_loss_1429_avge_mass "1429.3337"
-xref: spec_1_neutral_loss_1429_flag "false"
-xref: spec_1_neutral_loss_1429_composition "dHex(2) Hex(2) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1702
-name: dHex(2)Hex(3)HexA(1)HexNAc(2)Sulf(1)
-def: "DHex(2) Hex(3) HexA HexNAc(2) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=2&hex=3&hexa=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1702]
-xref: record_id "1702"
-xref: delta_mono_mass "1440.421936"
-xref: delta_avge_mass "1441.2766"
-xref: delta_composition "O(3) S dHex(2) Hex(3) HexA HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:55:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1441_mono_mass "1440.421936"
-xref: spec_1_neutral_loss_1441_avge_mass "1441.2766"
-xref: spec_1_neutral_loss_1441_flag "false"
-xref: spec_1_neutral_loss_1441_composition "O(3) S dHex(2) Hex(3) HexA HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1441_mono_mass "1440.421936"
-xref: spec_1_neutral_loss_1441_avge_mass "1441.2766"
-xref: spec_1_neutral_loss_1441_flag "false"
-xref: spec_1_neutral_loss_1441_composition "O(3) S dHex(2) Hex(3) HexA HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1703
-name: dHex(4)HexNAc(3)Kdn(1)
-def: "DHex(4) HexNAc(3) Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=4&hexnac=3&kdn=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1703]
-xref: record_id "1703"
-xref: delta_mono_mass "1443.538621"
-xref: delta_avge_mass "1444.345"
-xref: delta_composition "dHex(4) HexNAc(3) Kdn"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 15:56:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1444_mono_mass "1443.538621"
-xref: spec_1_neutral_loss_1444_avge_mass "1444.345"
-xref: spec_1_neutral_loss_1444_flag "false"
-xref: spec_1_neutral_loss_1444_composition "dHex(4) HexNAc(3) Kdn"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1444_mono_mass "1443.538621"
-xref: spec_1_neutral_loss_1444_avge_mass "1444.345"
-xref: spec_1_neutral_loss_1444_flag "false"
-xref: spec_1_neutral_loss_1444_composition "dHex(4) HexNAc(3) Kdn"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1705
-name: Hex(2)HexNAc(1)NeuGc(3)
-def: "Hex(2) HexNAc NeuGc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=1&neugc=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1705]
-xref: record_id "1705"
-xref: delta_mono_mass "1448.456013"
-xref: delta_avge_mass "1449.2357"
-xref: delta_composition "Hex(2) HexNAc(1) NeuGc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1449_mono_mass "1448.456013"
-xref: spec_1_neutral_loss_1449_avge_mass "1449.2357"
-xref: spec_1_neutral_loss_1449_flag "false"
-xref: spec_1_neutral_loss_1449_composition "Hex(2) HexNAc(1) NeuGc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1449_mono_mass "1448.456013"
-xref: spec_1_neutral_loss_1449_avge_mass "1449.2357"
-xref: spec_1_neutral_loss_1449_flag "false"
-xref: spec_1_neutral_loss_1449_composition "Hex(2) HexNAc(1) NeuGc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1706
-name: dHex(4)Hex(1)HexNAc(1)Kdn(2)
-def: "DHex(4) Hex HexNAc Kdn(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=4&hex=1&hexnac=1&kdn=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1706]
-xref: record_id "1706"
-xref: delta_mono_mass "1449.501567"
-xref: delta_avge_mass "1450.3032"
-xref: delta_composition "dHex(4) Hex HexNAc Kdn(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 15:56:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1450_mono_mass "1449.501567"
-xref: spec_1_neutral_loss_1450_avge_mass "1450.3032"
-xref: spec_1_neutral_loss_1450_flag "false"
-xref: spec_1_neutral_loss_1450_composition "dHex(4) Hex HexNAc Kdn(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1450_mono_mass "1449.501567"
-xref: spec_1_neutral_loss_1450_avge_mass "1450.3032"
-xref: spec_1_neutral_loss_1450_flag "false"
-xref: spec_1_neutral_loss_1450_composition "dHex(4) Hex HexNAc Kdn(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1707
-name: dHex(1)Hex(2)HexNAc(3)NeuAc(1)Sulf(1)
-def: "DHex Hex(2) HexNAc(3) NeuAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=2&hexnac=3&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1707]
-xref: record_id "1707"
-xref: delta_mono_mass "1450.453905"
-xref: delta_avge_mass "1451.3177"
-xref: delta_composition "O(3) S dHex Hex(2) HexNAc(3) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:55:33"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1451_mono_mass "1450.453905"
-xref: spec_1_neutral_loss_1451_avge_mass "1451.3177"
-xref: spec_1_neutral_loss_1451_flag "false"
-xref: spec_1_neutral_loss_1451_composition "O(3) S dHex Hex(2) HexNAc(3) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1451_mono_mass "1450.453905"
-xref: spec_1_neutral_loss_1451_avge_mass "1451.3177"
-xref: spec_1_neutral_loss_1451_flag "false"
-xref: spec_1_neutral_loss_1451_composition "O(3) S dHex Hex(2) HexNAc(3) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1708
-name: dHex(1)Hex(2)HexNAc(2)NeuAc(2)
-def: "DHex Hex(2) HexNAc(2) NeuAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=2&hexnac=2&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1708]
-xref: record_id "1708"
-xref: delta_mono_mass "1458.513134"
-xref: delta_avge_mass "1459.3166"
-xref: delta_composition "dHex(1) Hex(2) HexNAc(2) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1459_mono_mass "1458.513134"
-xref: spec_1_neutral_loss_1459_avge_mass "1459.3166"
-xref: spec_1_neutral_loss_1459_flag "false"
-xref: spec_1_neutral_loss_1459_composition "dHex(1) Hex(2) HexNAc(2) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1459_mono_mass "1458.513134"
-xref: spec_1_neutral_loss_1459_avge_mass "1459.3166"
-xref: spec_1_neutral_loss_1459_flag "false"
-xref: spec_1_neutral_loss_1459_composition "dHex(1) Hex(2) HexNAc(2) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1709
-name: dHex(3)Hex(1)HexNAc(3)Kdn(1)
-def: "DHex(3) Hex HexNAc(3) Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=3&hex=1&hexnac=3&kdn=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1709]
-xref: record_id "1709"
-xref: delta_mono_mass "1459.533535"
-xref: delta_avge_mass "1460.3444"
-xref: delta_composition "dHex(3) Hex HexNAc(3) Kdn"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 15:56:20"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1460_mono_mass "1459.533535"
-xref: spec_1_neutral_loss_1460_avge_mass "1460.3444"
-xref: spec_1_neutral_loss_1460_flag "false"
-xref: spec_1_neutral_loss_1460_composition "dHex(3) Hex HexNAc(3) Kdn"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1460_mono_mass "1459.533535"
-xref: spec_1_neutral_loss_1460_avge_mass "1460.3444"
-xref: spec_1_neutral_loss_1460_flag "false"
-xref: spec_1_neutral_loss_1460_composition "dHex(3) Hex HexNAc(3) Kdn"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1711
-name: Hex(3)HexNAc(3)NeuAc(1)Sulf(1)
-def: "Hex(3) HexNAc(3) NeuAc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=3&hexnac=3&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1711]
-xref: record_id "1711"
-xref: delta_mono_mass "1466.44882"
-xref: delta_avge_mass "1467.3171"
-xref: delta_composition "O(3) S Hex(3) HexNAc(3) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:55:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1467_mono_mass "1466.44882"
-xref: spec_1_neutral_loss_1467_avge_mass "1467.3171"
-xref: spec_1_neutral_loss_1467_flag "false"
-xref: spec_1_neutral_loss_1467_composition "O(3) S Hex(3) HexNAc(3) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1467_mono_mass "1466.44882"
-xref: spec_1_neutral_loss_1467_avge_mass "1467.3171"
-xref: spec_1_neutral_loss_1467_flag "false"
-xref: spec_1_neutral_loss_1467_composition "O(3) S Hex(3) HexNAc(3) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1712
-name: Hex(3)HexNAc(2)NeuAc(2)
-def: "Hex(3) HexNAc(2) NeuAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=2&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1712]
-xref: record_id "1712"
-xref: delta_mono_mass "1474.508049"
-xref: delta_avge_mass "1475.316"
-xref: delta_composition "Hex(3) HexNAc(2) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1475_mono_mass "1474.508049"
-xref: spec_1_neutral_loss_1475_avge_mass "1475.316"
-xref: spec_1_neutral_loss_1475_flag "false"
-xref: spec_1_neutral_loss_1475_composition "Hex(3) HexNAc(2) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1475_mono_mass "1474.508049"
-xref: spec_1_neutral_loss_1475_avge_mass "1475.316"
-xref: spec_1_neutral_loss_1475_flag "false"
-xref: spec_1_neutral_loss_1475_composition "Hex(3) HexNAc(2) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1713
-name: Hex(3)HexNAc(3)NeuGc(1)Sulf(1)
-def: "Hex(3) HexNAc(3) NeuGc Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=3&hexnac=3&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1713]
-xref: record_id "1713"
-xref: delta_mono_mass "1482.443734"
-xref: delta_avge_mass "1483.3165"
-xref: delta_composition "O(3) S Hex(3) HexNAc(3) NeuGc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:55:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1483_mono_mass "1482.443734"
-xref: spec_1_neutral_loss_1483_avge_mass "1483.3165"
-xref: spec_1_neutral_loss_1483_flag "false"
-xref: spec_1_neutral_loss_1483_composition "O(3) S Hex(3) HexNAc(3) NeuGc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1483_mono_mass "1482.443734"
-xref: spec_1_neutral_loss_1483_avge_mass "1483.3165"
-xref: spec_1_neutral_loss_1483_flag "false"
-xref: spec_1_neutral_loss_1483_composition "O(3) S Hex(3) HexNAc(3) NeuGc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1714
-name: dHex(1)Hex(2)HexNAc(2)NeuGc(2)
-def: "DHex Hex(2) HexNAc(2) NeuGc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=2&hexnac=2&neugc=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1714]
-xref: record_id "1714"
-xref: delta_mono_mass "1490.502964"
-xref: delta_avge_mass "1491.3154"
-xref: delta_composition "dHex(1) Hex(2) HexNAc(2) NeuGc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1491_mono_mass "1490.502964"
-xref: spec_1_neutral_loss_1491_avge_mass "1491.3154"
-xref: spec_1_neutral_loss_1491_flag "false"
-xref: spec_1_neutral_loss_1491_composition "dHex(1) Hex(2) HexNAc(2) NeuGc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1491_mono_mass "1490.502964"
-xref: spec_1_neutral_loss_1491_avge_mass "1491.3154"
-xref: spec_1_neutral_loss_1491_flag "false"
-xref: spec_1_neutral_loss_1491_composition "dHex(1) Hex(2) HexNAc(2) NeuGc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1715
-name: dHex(2)Hex(3)HexNAc(2)NeuGc(1)
-def: "DHex(2) Hex(3) HexNAc(2) NeuGc ---OR--- Hex(4) HexNAc(2) dHex NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=3&hexnac=2&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1715]
-xref: record_id "1715"
-xref: delta_mono_mass "1491.523365"
-xref: delta_avge_mass "1492.3432"
-xref: delta_composition "dHex(2) Hex(3) HexNAc(2) NeuGc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-17 15:37:46"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1492_mono_mass "1491.523365"
-xref: spec_1_neutral_loss_1492_avge_mass "1492.3432"
-xref: spec_1_neutral_loss_1492_flag "false"
-xref: spec_1_neutral_loss_1492_composition "dHex(2) Hex(3) HexNAc(2) NeuGc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1492_mono_mass "1491.523365"
-xref: spec_1_neutral_loss_1492_avge_mass "1492.3432"
-xref: spec_1_neutral_loss_1492_flag "false"
-xref: spec_1_neutral_loss_1492_composition "dHex(2) Hex(3) HexNAc(2) NeuGc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1716
-name: dHex(1)Hex(3)HexA(1)HexNAc(3)Sulf(1)
-def: "DHex Hex(3) HexA HexNAc(3) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=3&hexa=1&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1716]
-xref: record_id "1716"
-xref: delta_mono_mass "1497.4434"
-xref: delta_avge_mass "1498.3279"
-xref: delta_composition "O(3) S dHex Hex(3) HexA HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:54:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1498_mono_mass "1497.4434"
-xref: spec_1_neutral_loss_1498_avge_mass "1498.3279"
-xref: spec_1_neutral_loss_1498_flag "false"
-xref: spec_1_neutral_loss_1498_composition "O(3) S dHex Hex(3) HexA HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1498_mono_mass "1497.4434"
-xref: spec_1_neutral_loss_1498_avge_mass "1498.3279"
-xref: spec_1_neutral_loss_1498_flag "false"
-xref: spec_1_neutral_loss_1498_composition "O(3) S dHex Hex(3) HexA HexNAc(3)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1717
-name: Hex(2)HexNAc(3)NeuAc(2)
-def: "Hex(2) HexNAc(3) NeuAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=3&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1717]
-xref: record_id "1717"
-xref: delta_mono_mass "1515.534598"
-xref: delta_avge_mass "1516.3679"
-xref: delta_composition "Hex(2) HexNAc(3) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1516_mono_mass "1515.534598"
-xref: spec_1_neutral_loss_1516_avge_mass "1516.3679"
-xref: spec_1_neutral_loss_1516_flag "false"
-xref: spec_1_neutral_loss_1516_composition "Hex(2) HexNAc(3) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1516_mono_mass "1515.534598"
-xref: spec_1_neutral_loss_1516_avge_mass "1516.3679"
-xref: spec_1_neutral_loss_1516_flag "false"
-xref: spec_1_neutral_loss_1516_composition "Hex(2) HexNAc(3) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1718
-name: dHex(2)Hex(2)HexNAc(3)NeuAc(1)
-def: "DHex(2) Hex(2) HexNAc(3) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=2&hexnac=3&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1718]
-xref: record_id "1718"
-xref: delta_mono_mass "1516.554999"
-xref: delta_avge_mass "1517.3957"
-xref: delta_composition "dHex(2) Hex(2) HexNAc(3) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1517_mono_mass "1516.554999"
-xref: spec_1_neutral_loss_1517_avge_mass "1517.3957"
-xref: spec_1_neutral_loss_1517_flag "false"
-xref: spec_1_neutral_loss_1517_composition "dHex(2) Hex(2) HexNAc(3) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1517_mono_mass "1516.554999"
-xref: spec_1_neutral_loss_1517_avge_mass "1517.3957"
-xref: spec_1_neutral_loss_1517_flag "false"
-xref: spec_1_neutral_loss_1517_composition "dHex(2) Hex(2) HexNAc(3) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1719
-name: dHex(4)Hex(2)HexNAc(3)
-def: "DHex(4) Hex(2) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=4&hex=2&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1719]
-xref: record_id "1719"
-xref: delta_mono_mass "1517.5754"
-xref: delta_avge_mass "1518.4236"
-xref: delta_composition "dHex(4) Hex(2) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1518_mono_mass "1517.5754"
-xref: spec_1_neutral_loss_1518_avge_mass "1518.4236"
-xref: spec_1_neutral_loss_1518_flag "false"
-xref: spec_1_neutral_loss_1518_composition "dHex(4) Hex(2) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1518_mono_mass "1517.5754"
-xref: spec_1_neutral_loss_1518_avge_mass "1518.4236"
-xref: spec_1_neutral_loss_1518_flag "false"
-xref: spec_1_neutral_loss_1518_composition "dHex(4) Hex(2) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1720
-name: Hex(2)HexNAc(3)NeuAc(1)NeuGc(1)
-def: "Hex(2) HexNAc(3) NeuAc NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=3&neuac=1&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1720]
-xref: record_id "1720"
-xref: delta_mono_mass "1531.529513"
-xref: delta_avge_mass "1532.3673"
-xref: delta_composition "Hex(2) HexNAc(3) NeuAc(1) NeuGc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1532_mono_mass "1531.529513"
-xref: spec_1_neutral_loss_1532_avge_mass "1532.3673"
-xref: spec_1_neutral_loss_1532_flag "false"
-xref: spec_1_neutral_loss_1532_composition "Hex(2) HexNAc(3) NeuAc(1) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1532_mono_mass "1531.529513"
-xref: spec_1_neutral_loss_1532_avge_mass "1532.3673"
-xref: spec_1_neutral_loss_1532_flag "false"
-xref: spec_1_neutral_loss_1532_composition "Hex(2) HexNAc(3) NeuAc(1) NeuGc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1721
-name: dHex(2)Hex(2)HexNAc(3)NeuGc(1)
-def: "DHex(2) Hex(2) HexNAc(3) NeuGc ---OR--- Hex(3) HexNAc(3) dHex NeuAc ---OR--- Hex(2) HexNAc(4) dHex Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=2&hexnac=3&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1721]
-xref: record_id "1721"
-xref: delta_mono_mass "1532.549914"
-xref: delta_avge_mass "1533.3951"
-xref: delta_composition "dHex(2) Hex(2) HexNAc(3) NeuGc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-17 15:40:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1533_mono_mass "1532.549914"
-xref: spec_1_neutral_loss_1533_avge_mass "1533.3951"
-xref: spec_1_neutral_loss_1533_flag "false"
-xref: spec_1_neutral_loss_1533_composition "dHex(2) Hex(2) HexNAc(3) NeuGc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1533_mono_mass "1532.549914"
-xref: spec_1_neutral_loss_1533_avge_mass "1533.3951"
-xref: spec_1_neutral_loss_1533_flag "false"
-xref: spec_1_neutral_loss_1533_composition "dHex(2) Hex(2) HexNAc(3) NeuGc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1722
-name: dHex(3)Hex(3)HexNAc(3)
-def: "DHex(3) Hex(3) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=3&hex=3&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1722]
-xref: record_id "1722"
-xref: delta_mono_mass "1533.570315"
-xref: delta_avge_mass "1534.423"
-xref: delta_composition "dHex(3) Hex(3) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1534_mono_mass "1533.570315"
-xref: spec_1_neutral_loss_1534_avge_mass "1534.423"
-xref: spec_1_neutral_loss_1534_flag "false"
-xref: spec_1_neutral_loss_1534_composition "dHex(3) Hex(3) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1534_mono_mass "1533.570315"
-xref: spec_1_neutral_loss_1534_avge_mass "1534.423"
-xref: spec_1_neutral_loss_1534_flag "false"
-xref: spec_1_neutral_loss_1534_composition "dHex(3) Hex(3) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1723
-name: Hex(8)Phos(3)
-def: "Hex(8) Phos(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=3&hex=8&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1723]
-xref: record_id "1723"
-xref: delta_mono_mass "1536.321581"
-xref: delta_avge_mass "1537.0645"
-xref: delta_composition "H(3) O(9) P(3) Hex(8)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:43:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1537_mono_mass "1536.321581"
-xref: spec_1_neutral_loss_1537_avge_mass "1537.0645"
-xref: spec_1_neutral_loss_1537_flag "false"
-xref: spec_1_neutral_loss_1537_composition "H(3) O(9) P(3) Hex(8)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1537_mono_mass "1536.321581"
-xref: spec_1_neutral_loss_1537_avge_mass "1537.0645"
-xref: spec_1_neutral_loss_1537_flag "false"
-xref: spec_1_neutral_loss_1537_composition "H(3) O(9) P(3) Hex(8)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1724
-name: dHex(1)Hex(2)HexNAc(2)NeuAc(2)Sulf(1)
-def: "DHex Hex(2) HexNAc(2) NeuAc(2) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=2&hexnac=2&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1724]
-xref: record_id "1724"
-xref: delta_mono_mass "1538.469949"
-xref: delta_avge_mass "1539.3798"
-xref: delta_composition "O(3) S dHex Hex(2) HexNAc(2) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:54:39"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1539_mono_mass "1538.469949"
-xref: spec_1_neutral_loss_1539_avge_mass "1539.3798"
-xref: spec_1_neutral_loss_1539_flag "false"
-xref: spec_1_neutral_loss_1539_composition "O(3) S dHex Hex(2) HexNAc(2) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1539_mono_mass "1538.469949"
-xref: spec_1_neutral_loss_1539_avge_mass "1539.3798"
-xref: spec_1_neutral_loss_1539_flag "false"
-xref: spec_1_neutral_loss_1539_composition "O(3) S dHex Hex(2) HexNAc(2) NeuAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1725
-name: Hex(2)HexNAc(3)NeuGc(2)
-def: "Hex(2) HexNAc(3) NeuGc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=3&neugc=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1725]
-xref: record_id "1725"
-xref: delta_mono_mass "1547.524427"
-xref: delta_avge_mass "1548.3667"
-xref: delta_composition "Hex(2) HexNAc(3) NeuGc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1548_mono_mass "1547.524427"
-xref: spec_1_neutral_loss_1548_avge_mass "1548.3667"
-xref: spec_1_neutral_loss_1548_flag "false"
-xref: spec_1_neutral_loss_1548_composition "Hex(2) HexNAc(3) NeuGc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1548_mono_mass "1547.524427"
-xref: spec_1_neutral_loss_1548_avge_mass "1548.3667"
-xref: spec_1_neutral_loss_1548_flag "false"
-xref: spec_1_neutral_loss_1548_composition "Hex(2) HexNAc(3) NeuGc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1726
-name: dHex(4)Hex(2)HexNAc(2)Kdn(1)
-def: "DHex(4) Hex(2) HexNAc(2) Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=4&hex=2&hexnac=2&kdn=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1726]
-xref: record_id "1726"
-xref: delta_mono_mass "1564.564895"
-xref: delta_avge_mass "1565.4337"
-xref: delta_composition "dHex(4) Hex(2) HexNAc(2) Kdn"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 15:56:06"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1565_mono_mass "1564.564895"
-xref: spec_1_neutral_loss_1565_avge_mass "1565.4337"
-xref: spec_1_neutral_loss_1565_flag "false"
-xref: spec_1_neutral_loss_1565_composition "dHex(4) Hex(2) HexNAc(2) Kdn"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1565_mono_mass "1564.564895"
-xref: spec_1_neutral_loss_1565_avge_mass "1565.4337"
-xref: spec_1_neutral_loss_1565_flag "false"
-xref: spec_1_neutral_loss_1565_composition "dHex(4) Hex(2) HexNAc(2) Kdn"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1727
-name: dHex(1)Hex(2)HexNAc(4)NeuAc(1)
-def: "DHex Hex(2) HexNAc(4) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=2&hexnac=4&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1727]
-xref: record_id "1727"
-xref: delta_mono_mass "1573.576463"
-xref: delta_avge_mass "1574.4471"
-xref: delta_composition "dHex(1) Hex(2) HexNAc(4) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1574_mono_mass "1573.576463"
-xref: spec_1_neutral_loss_1574_avge_mass "1574.4471"
-xref: spec_1_neutral_loss_1574_flag "false"
-xref: spec_1_neutral_loss_1574_composition "dHex(1) Hex(2) HexNAc(4) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1574_mono_mass "1573.576463"
-xref: spec_1_neutral_loss_1574_avge_mass "1574.4471"
-xref: spec_1_neutral_loss_1574_flag "false"
-xref: spec_1_neutral_loss_1574_composition "dHex(1) Hex(2) HexNAc(4) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1728
-name: dHex(3)Hex(2)HexNAc(4)
-def: "DHex(3) Hex(2) HexNAc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=3&hex=2&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1728]
-xref: record_id "1728"
-xref: delta_mono_mass "1574.596864"
-xref: delta_avge_mass "1575.4749"
-xref: delta_composition "dHex(3) Hex(2) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1575_mono_mass "1574.596864"
-xref: spec_1_neutral_loss_1575_avge_mass "1575.4749"
-xref: spec_1_neutral_loss_1575_flag "false"
-xref: spec_1_neutral_loss_1575_composition "dHex(3) Hex(2) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1575_mono_mass "1574.596864"
-xref: spec_1_neutral_loss_1575_avge_mass "1575.4749"
-xref: spec_1_neutral_loss_1575_flag "false"
-xref: spec_1_neutral_loss_1575_composition "dHex(3) Hex(2) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1729
-name: Hex(1)HexNAc(1)NeuGc(4)
-def: "Hex HexNAc NeuGc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=1&neugc=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1729]
-xref: record_id "1729"
-xref: delta_mono_mass "1593.493521"
-xref: delta_avge_mass "1594.349"
-xref: delta_composition "Hex(1) HexNAc(1) NeuGc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1594_mono_mass "1593.493521"
-xref: spec_1_neutral_loss_1594_avge_mass "1594.349"
-xref: spec_1_neutral_loss_1594_flag "false"
-xref: spec_1_neutral_loss_1594_composition "Hex(1) HexNAc(1) NeuGc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1594_mono_mass "1593.493521"
-xref: spec_1_neutral_loss_1594_avge_mass "1594.349"
-xref: spec_1_neutral_loss_1594_flag "false"
-xref: spec_1_neutral_loss_1594_composition "Hex(1) HexNAc(1) NeuGc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1730
-name: dHex(4)Hex(1)HexNAc(3)Kdn(1)
-def: "DHex(4) Hex HexNAc(3) Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=4&hex=1&hexnac=3&kdn=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1730]
-xref: record_id "1730"
-xref: delta_mono_mass "1605.591444"
-xref: delta_avge_mass "1606.4856"
-xref: delta_composition "dHex(4) Hex HexNAc(3) Kdn"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 15:55:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1606_mono_mass "1605.591444"
-xref: spec_1_neutral_loss_1606_avge_mass "1606.4856"
-xref: spec_1_neutral_loss_1606_flag "false"
-xref: spec_1_neutral_loss_1606_composition "dHex(4) Hex HexNAc(3) Kdn"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1606_mono_mass "1605.591444"
-xref: spec_1_neutral_loss_1606_avge_mass "1606.4856"
-xref: spec_1_neutral_loss_1606_flag "false"
-xref: spec_1_neutral_loss_1606_composition "dHex(4) Hex HexNAc(3) Kdn"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1732
-name: Hex(4)HexNAc(4)Sulf(2)
-def: "Hex(4) HexNAc(4) Sulf(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=2&hex=4&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1732]
-xref: record_id "1732"
-xref: delta_mono_mass "1620.442414"
-xref: delta_avge_mass "1621.4589"
-xref: delta_composition "O(6) S(2) Hex(4) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 10:35:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1621_mono_mass "1620.442414"
-xref: spec_1_neutral_loss_1621_avge_mass "1621.4589"
-xref: spec_1_neutral_loss_1621_flag "false"
-xref: spec_1_neutral_loss_1621_composition "O(6) S(2) Hex(4) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1621_mono_mass "1620.442414"
-xref: spec_1_neutral_loss_1621_avge_mass "1621.4589"
-xref: spec_1_neutral_loss_1621_flag "false"
-xref: spec_1_neutral_loss_1621_composition "O(6) S(2) Hex(4) HexNAc(4)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1733
-name: dHex(3)Hex(2)HexNAc(3)Kdn(1)
-def: "DHex(3) Hex(2) HexNAc(3) Kdn ---OR--- Hex(3) HexNAc(2) dHex(3) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=3&hex=2&hexnac=3&kdn=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1733]
-xref: record_id "1733"
-xref: delta_mono_mass "1621.586359"
-xref: delta_avge_mass "1622.485"
-xref: delta_composition "dHex(3) Hex(2) HexNAc(3) Kdn"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-22 10:37:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1622_mono_mass "1621.586359"
-xref: spec_1_neutral_loss_1622_avge_mass "1622.485"
-xref: spec_1_neutral_loss_1622_flag "false"
-xref: spec_1_neutral_loss_1622_composition "dHex(3) Hex(2) HexNAc(3) Kdn"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1622_mono_mass "1621.586359"
-xref: spec_1_neutral_loss_1622_avge_mass "1622.485"
-xref: spec_1_neutral_loss_1622_flag "false"
-xref: spec_1_neutral_loss_1622_composition "dHex(3) Hex(2) HexNAc(3) Kdn"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1735
-name: dHex(2)Hex(2)HexNAc(5)
-def: "DHex(2) Hex(2) HexNAc(5)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=2&hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1735]
-xref: record_id "1735"
-xref: delta_mono_mass "1631.618328"
-xref: delta_avge_mass "1632.5262"
-xref: delta_composition "dHex(2) Hex(2) HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1632_mono_mass "1631.618328"
-xref: spec_1_neutral_loss_1632_avge_mass "1632.5262"
-xref: spec_1_neutral_loss_1632_flag "false"
-xref: spec_1_neutral_loss_1632_composition "dHex(2) Hex(2) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1632_mono_mass "1631.618328"
-xref: spec_1_neutral_loss_1632_avge_mass "1632.5262"
-xref: spec_1_neutral_loss_1632_flag "false"
-xref: spec_1_neutral_loss_1632_composition "dHex(2) Hex(2) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1736
-name: dHex(2)Hex(3)HexA(1)HexNAc(3)Sulf(1)
-def: "DHex(2) Hex(3) HexA HexNAc(3) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=2&hex=3&hexa=1&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1736]
-xref: record_id "1736"
-xref: delta_mono_mass "1643.501309"
-xref: delta_avge_mass "1644.4691"
-xref: delta_composition "O(3) S dHex(2) Hex(3) HexA HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:54:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1644_mono_mass "1643.501309"
-xref: spec_1_neutral_loss_1644_avge_mass "1644.4691"
-xref: spec_1_neutral_loss_1644_flag "false"
-xref: spec_1_neutral_loss_1644_composition "O(3) S dHex(2) Hex(3) HexA HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1644_mono_mass "1643.501309"
-xref: spec_1_neutral_loss_1644_avge_mass "1644.4691"
-xref: spec_1_neutral_loss_1644_flag "false"
-xref: spec_1_neutral_loss_1644_composition "O(3) S dHex(2) Hex(3) HexA HexNAc(3)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1737
-name: dHex(1)Hex(4)HexA(1)HexNAc(3)Sulf(1)
-def: "DHex Hex(4) HexA HexNAc(3) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=4&hexa=1&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1737]
-xref: record_id "1737"
-xref: delta_mono_mass "1659.496223"
-xref: delta_avge_mass "1660.4685"
-xref: delta_composition "O(3) S dHex Hex(4) HexA HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:54:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1660_mono_mass "1659.496223"
-xref: spec_1_neutral_loss_1660_avge_mass "1660.4685"
-xref: spec_1_neutral_loss_1660_flag "false"
-xref: spec_1_neutral_loss_1660_composition "O(3) S dHex Hex(4) HexA HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1660_mono_mass "1659.496223"
-xref: spec_1_neutral_loss_1660_avge_mass "1660.4685"
-xref: spec_1_neutral_loss_1660_flag "false"
-xref: spec_1_neutral_loss_1660_composition "O(3) S dHex Hex(4) HexA HexNAc(3)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1738
-name: Hex(3)HexNAc(3)NeuAc(2)
-def: "Hex(3) HexNAc(3) NeuAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=3&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1738]
-xref: record_id "1738"
-xref: delta_mono_mass "1677.587422"
-xref: delta_avge_mass "1678.5085"
-xref: delta_composition "Hex(3) HexNAc(3) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1678_mono_mass "1677.587422"
-xref: spec_1_neutral_loss_1678_avge_mass "1678.5085"
-xref: spec_1_neutral_loss_1678_flag "false"
-xref: spec_1_neutral_loss_1678_composition "Hex(3) HexNAc(3) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1678_mono_mass "1677.587422"
-xref: spec_1_neutral_loss_1678_avge_mass "1678.5085"
-xref: spec_1_neutral_loss_1678_flag "false"
-xref: spec_1_neutral_loss_1678_composition "Hex(3) HexNAc(3) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1739
-name: dHex(2)Hex(3)HexNAc(3)NeuAc(1)
-def: "DHex(2) Hex(3) HexNAc(3) NeuAc ---OR--- Hex(2) HexNAc(4) dHex(2) Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=3&hexnac=3&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1739]
-xref: record_id "1739"
-xref: delta_mono_mass "1678.607823"
-xref: delta_avge_mass "1679.5363"
-xref: delta_composition "dHex(2) Hex(3) HexNAc(3) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-22 10:51:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1679_mono_mass "1678.607823"
-xref: spec_1_neutral_loss_1679_avge_mass "1679.5363"
-xref: spec_1_neutral_loss_1679_flag "false"
-xref: spec_1_neutral_loss_1679_composition "dHex(2) Hex(3) HexNAc(3) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1679_mono_mass "1678.607823"
-xref: spec_1_neutral_loss_1679_avge_mass "1679.5363"
-xref: spec_1_neutral_loss_1679_flag "false"
-xref: spec_1_neutral_loss_1679_composition "dHex(2) Hex(3) HexNAc(3) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1740
-name: dHex(4)Hex(3)HexNAc(3)
-def: "DHex(4) Hex(3) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=4&hex=3&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1740]
-xref: record_id "1740"
-xref: delta_mono_mass "1679.628224"
-xref: delta_avge_mass "1680.5642"
-xref: delta_composition "dHex(4) Hex(3) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1680_mono_mass "1679.628224"
-xref: spec_1_neutral_loss_1680_avge_mass "1680.5642"
-xref: spec_1_neutral_loss_1680_flag "false"
-xref: spec_1_neutral_loss_1680_composition "dHex(4) Hex(3) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1680_mono_mass "1679.628224"
-xref: spec_1_neutral_loss_1680_avge_mass "1680.5642"
-xref: spec_1_neutral_loss_1680_flag "false"
-xref: spec_1_neutral_loss_1680_composition "dHex(4) Hex(3) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1742
-name: Hex(9)Phos(3)
-def: "Hex(9) Phos(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=3&hex=9&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1742]
-xref: record_id "1742"
-xref: delta_mono_mass "1698.374404"
-xref: delta_avge_mass "1699.2051"
-xref: delta_composition "H(3) O(9) P(3) Hex(9)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:47:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1699_mono_mass "1698.374404"
-xref: spec_1_neutral_loss_1699_avge_mass "1699.2051"
-xref: spec_1_neutral_loss_1699_flag "false"
-xref: spec_1_neutral_loss_1699_composition "H(3) O(9) P(3) Hex(9)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1699_mono_mass "1698.374404"
-xref: spec_1_neutral_loss_1699_avge_mass "1699.2051"
-xref: spec_1_neutral_loss_1699_flag "false"
-xref: spec_1_neutral_loss_1699_composition "H(3) O(9) P(3) Hex(9)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1743
-name: dHex(2)HexNAc(7)
-def: "DHex(2) HexNAc(7)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hexnac=7&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1743]
-xref: record_id "1743"
-xref: delta_mono_mass "1713.671426"
-xref: delta_avge_mass "1714.63"
-xref: delta_composition "dHex(2) HexNAc(7)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1714_mono_mass "1713.671426"
-xref: spec_1_neutral_loss_1714_avge_mass "1714.63"
-xref: spec_1_neutral_loss_1714_flag "false"
-xref: spec_1_neutral_loss_1714_composition "dHex(2) HexNAc(7)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1714_mono_mass "1713.671426"
-xref: spec_1_neutral_loss_1714_avge_mass "1714.63"
-xref: spec_1_neutral_loss_1714_flag "false"
-xref: spec_1_neutral_loss_1714_composition "dHex(2) HexNAc(7)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1744
-name: Hex(2)HexNAc(1)NeuGc(4)
-def: "Hex(2) HexNAc NeuGc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=1&neugc=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1744]
-xref: record_id "1744"
-xref: delta_mono_mass "1755.546345"
-xref: delta_avge_mass "1756.4896"
-xref: delta_composition "Hex(2) HexNAc(1) NeuGc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1756_mono_mass "1755.546345"
-xref: spec_1_neutral_loss_1756_avge_mass "1756.4896"
-xref: spec_1_neutral_loss_1756_flag "false"
-xref: spec_1_neutral_loss_1756_composition "Hex(2) HexNAc(1) NeuGc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1756_mono_mass "1755.546345"
-xref: spec_1_neutral_loss_1756_avge_mass "1756.4896"
-xref: spec_1_neutral_loss_1756_flag "false"
-xref: spec_1_neutral_loss_1756_composition "Hex(2) HexNAc(1) NeuGc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1745
-name: Hex(3)HexNAc(3)NeuAc(2)Sulf(1)
-def: "Hex(3) HexNAc(3) NeuAc(2) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=3&hexnac=3&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1745]
-xref: record_id "1745"
-xref: delta_mono_mass "1757.544236"
-xref: delta_avge_mass "1758.5717"
-xref: delta_composition "O(3) S Hex(3) HexNAc(3) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:54:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1758_mono_mass "1757.544236"
-xref: spec_1_neutral_loss_1758_avge_mass "1758.5717"
-xref: spec_1_neutral_loss_1758_flag "false"
-xref: spec_1_neutral_loss_1758_composition "O(3) S Hex(3) HexNAc(3) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1758_mono_mass "1757.544236"
-xref: spec_1_neutral_loss_1758_avge_mass "1758.5717"
-xref: spec_1_neutral_loss_1758_flag "false"
-xref: spec_1_neutral_loss_1758_composition "O(3) S Hex(3) HexNAc(3) NeuAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1746
-name: dHex(2)Hex(3)HexNAc(5)
-def: "DHex(2) Hex(3) HexNAc(5)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=3&hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1746]
-xref: record_id "1746"
-xref: delta_mono_mass "1793.671151"
-xref: delta_avge_mass "1794.6668"
-xref: delta_composition "dHex(2) Hex(3) HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-24 13:43:21"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1794_mono_mass "1793.671151"
-xref: spec_1_neutral_loss_1794_avge_mass "1794.6668"
-xref: spec_1_neutral_loss_1794_flag "false"
-xref: spec_1_neutral_loss_1794_composition "dHex(2) Hex(3) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1794_mono_mass "1793.671151"
-xref: spec_1_neutral_loss_1794_avge_mass "1794.6668"
-xref: spec_1_neutral_loss_1794_flag "false"
-xref: spec_1_neutral_loss_1794_composition "dHex(2) Hex(3) HexNAc(5)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1794_mono_mass "1793.671151"
-xref: spec_2_neutral_loss_1794_avge_mass "1794.6668"
-xref: spec_2_neutral_loss_1794_flag "false"
-xref: spec_2_neutral_loss_1794_composition "dHex(2) Hex(3) HexNAc(5)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1747
-name: dHex(1)Hex(2)HexNAc(2)NeuGc(3)
-def: "DHex Hex(2) HexNAc(2) NeuGc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=2&hexnac=2&neugc=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1747]
-xref: record_id "1747"
-xref: delta_mono_mass "1797.593295"
-xref: delta_avge_mass "1798.5694"
-xref: delta_composition "dHex(1) Hex(2) HexNAc(2) NeuGc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1798_mono_mass "1797.593295"
-xref: spec_1_neutral_loss_1798_avge_mass "1798.5694"
-xref: spec_1_neutral_loss_1798_flag "false"
-xref: spec_1_neutral_loss_1798_composition "dHex(1) Hex(2) HexNAc(2) NeuGc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1798_mono_mass "1797.593295"
-xref: spec_1_neutral_loss_1798_avge_mass "1798.5694"
-xref: spec_1_neutral_loss_1798_flag "false"
-xref: spec_1_neutral_loss_1798_composition "dHex(1) Hex(2) HexNAc(2) NeuGc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1748
-name: dHex(2)Hex(4)HexA(1)HexNAc(3)Sulf(1)
-def: "DHex(2) Hex(4) HexA HexNAc(3) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=2&hex=4&hexa=1&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1748]
-xref: record_id "1748"
-xref: delta_mono_mass "1805.554132"
-xref: delta_avge_mass "1806.6097"
-xref: delta_composition "O(3) S dHex(2) Hex(4) HexA HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:53:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1806_mono_mass "1805.554132"
-xref: spec_1_neutral_loss_1806_avge_mass "1806.6097"
-xref: spec_1_neutral_loss_1806_flag "false"
-xref: spec_1_neutral_loss_1806_composition "O(3) S dHex(2) Hex(4) HexA HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1806_mono_mass "1805.554132"
-xref: spec_1_neutral_loss_1806_avge_mass "1806.6097"
-xref: spec_1_neutral_loss_1806_flag "false"
-xref: spec_1_neutral_loss_1806_composition "O(3) S dHex(2) Hex(4) HexA HexNAc(3)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1749
-name: Hex(2)HexNAc(3)NeuAc(3)
-def: "Hex(2) HexNAc(3) NeuAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=3&neuac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1749]
-xref: record_id "1749"
-xref: delta_mono_mass "1806.630015"
-xref: delta_avge_mass "1807.6225"
-xref: delta_composition "Hex(2) HexNAc(3) NeuAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1807_mono_mass "1806.630015"
-xref: spec_1_neutral_loss_1807_avge_mass "1807.6225"
-xref: spec_1_neutral_loss_1807_flag "false"
-xref: spec_1_neutral_loss_1807_composition "Hex(2) HexNAc(3) NeuAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1807_mono_mass "1806.630015"
-xref: spec_1_neutral_loss_1807_avge_mass "1807.6225"
-xref: spec_1_neutral_loss_1807_flag "false"
-xref: spec_1_neutral_loss_1807_composition "Hex(2) HexNAc(3) NeuAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1750
-name: dHex(1)Hex(3)HexNAc(3)NeuAc(2)
-def: "DHex Hex(3) HexNAc(3) NeuAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexnac=3&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1750]
-xref: record_id "1750"
-xref: delta_mono_mass "1823.64533"
-xref: delta_avge_mass "1824.6497"
-xref: delta_composition "dHex(1) Hex(3) HexNAc(3) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1824_mono_mass "1823.64533"
-xref: spec_1_neutral_loss_1824_avge_mass "1824.6497"
-xref: spec_1_neutral_loss_1824_flag "false"
-xref: spec_1_neutral_loss_1824_composition "dHex(1) Hex(3) HexNAc(3) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1824_mono_mass "1823.64533"
-xref: spec_1_neutral_loss_1824_avge_mass "1824.6497"
-xref: spec_1_neutral_loss_1824_flag "false"
-xref: spec_1_neutral_loss_1824_composition "dHex(1) Hex(3) HexNAc(3) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1751
-name: dHex(3)Hex(3)HexNAc(3)NeuAc(1)
-def: "DHex(3) Hex(3) HexNAc(3) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=3&hex=3&hexnac=3&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1751]
-xref: record_id "1751"
-xref: delta_mono_mass "1824.665732"
-xref: delta_avge_mass "1825.6775"
-xref: delta_composition "dHex(3) Hex(3) HexNAc(3) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1825_mono_mass "1824.665732"
-xref: spec_1_neutral_loss_1825_avge_mass "1825.6775"
-xref: spec_1_neutral_loss_1825_flag "false"
-xref: spec_1_neutral_loss_1825_composition "dHex(3) Hex(3) HexNAc(3) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1825_mono_mass "1824.665732"
-xref: spec_1_neutral_loss_1825_avge_mass "1825.6775"
-xref: spec_1_neutral_loss_1825_flag "false"
-xref: spec_1_neutral_loss_1825_composition "dHex(3) Hex(3) HexNAc(3) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1752
-name: Hex(2)HexNAc(3)NeuGc(3)
-def: "Hex(2) HexNAc(3) NeuGc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=2&hexnac=3&neugc=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1752]
-xref: record_id "1752"
-xref: delta_mono_mass "1854.614759"
-xref: delta_avge_mass "1855.6207"
-xref: delta_composition "Hex(2) HexNAc(3) NeuGc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1855_mono_mass "1854.614759"
-xref: spec_1_neutral_loss_1855_avge_mass "1855.6207"
-xref: spec_1_neutral_loss_1855_flag "false"
-xref: spec_1_neutral_loss_1855_composition "Hex(2) HexNAc(3) NeuGc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1855_mono_mass "1854.614759"
-xref: spec_1_neutral_loss_1855_avge_mass "1855.6207"
-xref: spec_1_neutral_loss_1855_flag "false"
-xref: spec_1_neutral_loss_1855_composition "Hex(2) HexNAc(3) NeuGc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1753
-name: Hex(10)Phos(3)
-def: "Hex(10) Phos(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?phosphate=3&hex=10&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1753]
-xref: record_id "1753"
-xref: delta_mono_mass "1860.427228"
-xref: delta_avge_mass "1861.3457"
-xref: delta_composition "H(3) O(9) P(3) Hex(10)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:51:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1861_mono_mass "1860.427228"
-xref: spec_1_neutral_loss_1861_avge_mass "1861.3457"
-xref: spec_1_neutral_loss_1861_flag "false"
-xref: spec_1_neutral_loss_1861_composition "H(3) O(9) P(3) Hex(10)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1861_mono_mass "1860.427228"
-xref: spec_1_neutral_loss_1861_avge_mass "1861.3457"
-xref: spec_1_neutral_loss_1861_flag "false"
-xref: spec_1_neutral_loss_1861_composition "H(3) O(9) P(3) Hex(10)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1754
-name: dHex(1)Hex(2)HexNAc(4)NeuAc(2)
-def: "DHex Hex(2) HexNAc(4) NeuAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=2&hexnac=4&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1754]
-xref: record_id "1754"
-xref: delta_mono_mass "1864.67188"
-xref: delta_avge_mass "1865.7016"
-xref: delta_composition "dHex(1) Hex(2) HexNAc(4) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1865_mono_mass "1864.67188"
-xref: spec_1_neutral_loss_1865_avge_mass "1865.7016"
-xref: spec_1_neutral_loss_1865_flag "false"
-xref: spec_1_neutral_loss_1865_composition "dHex(1) Hex(2) HexNAc(4) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1865_mono_mass "1864.67188"
-xref: spec_1_neutral_loss_1865_avge_mass "1865.7016"
-xref: spec_1_neutral_loss_1865_flag "false"
-xref: spec_1_neutral_loss_1865_composition "dHex(1) Hex(2) HexNAc(4) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1755
-name: Hex(1)HexNAc(1)NeuGc(5)
-def: "Hex HexNAc NeuGc(5)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=1&hexnac=1&neugc=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1755]
-xref: record_id "1755"
-xref: delta_mono_mass "1900.583852"
-xref: delta_avge_mass "1901.603"
-xref: delta_composition "Hex(1) HexNAc(1) NeuGc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1901_mono_mass "1900.583852"
-xref: spec_1_neutral_loss_1901_avge_mass "1901.603"
-xref: spec_1_neutral_loss_1901_flag "false"
-xref: spec_1_neutral_loss_1901_composition "Hex(1) HexNAc(1) NeuGc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1901_mono_mass "1900.583852"
-xref: spec_1_neutral_loss_1901_avge_mass "1901.603"
-xref: spec_1_neutral_loss_1901_flag "false"
-xref: spec_1_neutral_loss_1901_composition "Hex(1) HexNAc(1) NeuGc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1756
-name: Hex(4)HexNAc(4)NeuAc(1)Sulf(2)
-def: "Hex(4) HexNAc(4) NeuAc Sulf(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=2&hex=4&hexnac=4&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1756]
-xref: record_id "1756"
-xref: delta_mono_mass "1911.53783"
-xref: delta_avge_mass "1912.7135"
-xref: delta_composition "O(6) S(2) Hex(4) HexNAc(4) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:50:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1912_mono_mass "1911.53783"
-xref: spec_1_neutral_loss_1912_avge_mass "1912.7135"
-xref: spec_1_neutral_loss_1912_flag "false"
-xref: spec_1_neutral_loss_1912_composition "O(6) S(2) Hex(4) HexNAc(4) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1912_mono_mass "1911.53783"
-xref: spec_1_neutral_loss_1912_avge_mass "1912.7135"
-xref: spec_1_neutral_loss_1912_flag "false"
-xref: spec_1_neutral_loss_1912_composition "O(6) S(2) Hex(4) HexNAc(4) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1757
-name: Hex(4)HexNAc(4)NeuGc(1)Sulf(2)
-def: "Hex(4) HexNAc(4) NeuGc Sulf(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=2&hex=4&hexnac=4&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1757]
-xref: record_id "1757"
-xref: delta_mono_mass "1927.532745"
-xref: delta_avge_mass "1928.7129"
-xref: delta_composition "O(6) S(2) Hex(4) HexNAc(4) NeuGc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:50:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1928_mono_mass "1927.532745"
-xref: spec_1_neutral_loss_1928_avge_mass "1928.7129"
-xref: spec_1_neutral_loss_1928_flag "false"
-xref: spec_1_neutral_loss_1928_composition "O(6) S(2) Hex(4) HexNAc(4) NeuGc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1928_mono_mass "1927.532745"
-xref: spec_1_neutral_loss_1928_avge_mass "1928.7129"
-xref: spec_1_neutral_loss_1928_flag "false"
-xref: spec_1_neutral_loss_1928_composition "O(6) S(2) Hex(4) HexNAc(4) NeuGc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1758
-name: dHex(2)Hex(3)HexNAc(3)NeuAc(2)
-def: "DHex(2) Hex(3) HexNAc(3) NeuAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=3&hexnac=3&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1758]
-xref: record_id "1758"
-xref: delta_mono_mass "1969.703239"
-xref: delta_avge_mass "1970.7909"
-xref: delta_composition "dHex(2) Hex(3) HexNAc(3) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1970_mono_mass "1969.703239"
-xref: spec_1_neutral_loss_1970_avge_mass "1970.7909"
-xref: spec_1_neutral_loss_1970_flag "false"
-xref: spec_1_neutral_loss_1970_composition "dHex(2) Hex(3) HexNAc(3) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1970_mono_mass "1969.703239"
-xref: spec_1_neutral_loss_1970_avge_mass "1970.7909"
-xref: spec_1_neutral_loss_1970_flag "false"
-xref: spec_1_neutral_loss_1970_composition "dHex(2) Hex(3) HexNAc(3) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1759
-name: Hex(4)HexNAc(4)NeuAc(1)Sulf(3)
-def: "Hex(4) HexNAc(4) NeuAc Sulf(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=3&hex=4&hexnac=4&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1759]
-xref: record_id "1759"
-xref: delta_mono_mass "1991.494645"
-xref: delta_avge_mass "1992.7767"
-xref: delta_composition "O(9) S(3) Hex(4) HexNAc(4) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:50:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1992_mono_mass "1991.494645"
-xref: spec_1_neutral_loss_1992_avge_mass "1992.7767"
-xref: spec_1_neutral_loss_1992_flag "false"
-xref: spec_1_neutral_loss_1992_composition "O(9) S(3) Hex(4) HexNAc(4) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1992_mono_mass "1991.494645"
-xref: spec_1_neutral_loss_1992_avge_mass "1992.7767"
-xref: spec_1_neutral_loss_1992_flag "false"
-xref: spec_1_neutral_loss_1992_composition "O(9) S(3) Hex(4) HexNAc(4) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1760
-name: dHex(2)Hex(2)HexNAc(2)
-def: "DHex(2) Hex(2) HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=2&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1760]
-xref: record_id "1760"
-xref: delta_mono_mass "1022.38021"
-xref: delta_avge_mass "1022.9486"
-xref: delta_composition "dHex(2) Hex(2) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1023_mono_mass "1022.38021"
-xref: spec_1_neutral_loss_1023_avge_mass "1022.9486"
-xref: spec_1_neutral_loss_1023_flag "false"
-xref: spec_1_neutral_loss_1023_composition "dHex(2) Hex(2) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1023_mono_mass "1022.38021"
-xref: spec_1_neutral_loss_1023_avge_mass "1022.9486"
-xref: spec_1_neutral_loss_1023_flag "false"
-xref: spec_1_neutral_loss_1023_composition "dHex(2) Hex(2) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1023_mono_mass "1022.38021"
-xref: spec_2_neutral_loss_1023_avge_mass "1022.9486"
-xref: spec_2_neutral_loss_1023_flag "false"
-xref: spec_2_neutral_loss_1023_composition "dHex(2) Hex(2) HexNAc(2)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1761
-name: dHex(1)Hex(3)HexNAc(2)
-def: "DHex Hex(3) HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1761]
-xref: record_id "1761"
-xref: delta_mono_mass "1038.375125"
-xref: delta_avge_mass "1038.948"
-xref: delta_composition "dHex(1) Hex(3) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1039_mono_mass "1038.375125"
-xref: spec_1_neutral_loss_1039_avge_mass "1038.948"
-xref: spec_1_neutral_loss_1039_flag "false"
-xref: spec_1_neutral_loss_1039_composition "dHex(1) Hex(3) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1039_mono_mass "1038.375125"
-xref: spec_1_neutral_loss_1039_avge_mass "1038.948"
-xref: spec_1_neutral_loss_1039_flag "false"
-xref: spec_1_neutral_loss_1039_composition "dHex(1) Hex(3) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1039_mono_mass "1038.375125"
-xref: spec_2_neutral_loss_1039_avge_mass "1038.948"
-xref: spec_2_neutral_loss_1039_flag "false"
-xref: spec_2_neutral_loss_1039_composition "dHex(1) Hex(3) HexNAc(2)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1762
-name: dHex(1)Hex(2)HexNAc(3)
-def: "DHex Hex(2) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=2&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1762]
-xref: record_id "1762"
-xref: delta_mono_mass "1079.401674"
-xref: delta_avge_mass "1080"
-xref: delta_composition "dHex(1) Hex(2) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1080_mono_mass "1079.401674"
-xref: spec_1_neutral_loss_1080_avge_mass "1080"
-xref: spec_1_neutral_loss_1080_flag "false"
-xref: spec_1_neutral_loss_1080_composition "dHex(1) Hex(2) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1080_mono_mass "1079.401674"
-xref: spec_1_neutral_loss_1080_avge_mass "1080"
-xref: spec_1_neutral_loss_1080_flag "false"
-xref: spec_1_neutral_loss_1080_composition "dHex(1) Hex(2) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1080_mono_mass "1079.401674"
-xref: spec_2_neutral_loss_1080_avge_mass "1080"
-xref: spec_2_neutral_loss_1080_flag "false"
-xref: spec_2_neutral_loss_1080_composition "dHex(1) Hex(2) HexNAc(3)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1763
-name: Hex(3)HexNAc(3)
-def: "Hex(3) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1763]
-xref: record_id "1763"
-xref: delta_mono_mass "1095.396588"
-xref: delta_avge_mass "1095.9994"
-xref: delta_composition "Hex(3) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1096_mono_mass "1095.396588"
-xref: spec_1_neutral_loss_1096_avge_mass "1095.9994"
-xref: spec_1_neutral_loss_1096_flag "false"
-xref: spec_1_neutral_loss_1096_composition "Hex(3) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1096_mono_mass "1095.396588"
-xref: spec_1_neutral_loss_1096_avge_mass "1095.9994"
-xref: spec_1_neutral_loss_1096_flag "false"
-xref: spec_1_neutral_loss_1096_composition "Hex(3) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1096_mono_mass "1095.396588"
-xref: spec_2_neutral_loss_1096_avge_mass "1095.9994"
-xref: spec_2_neutral_loss_1096_flag "false"
-xref: spec_2_neutral_loss_1096_composition "Hex(3) HexNAc(3)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1764
-name: dHex(1)Hex(3)HexNAc(2)Sulf(1)
-def: "DHex Hex(3) HexNAc(2) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=3&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1764]
-xref: record_id "1764"
-xref: delta_mono_mass "1118.331939"
-xref: delta_avge_mass "1119.0112"
-xref: delta_composition "O(3) S dHex Hex(3) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-06 09:49:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1119_mono_mass "1118.331939"
-xref: spec_1_neutral_loss_1119_avge_mass "1119.0112"
-xref: spec_1_neutral_loss_1119_flag "false"
-xref: spec_1_neutral_loss_1119_composition "O(3) S dHex Hex(3) HexNAc(2)"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1119_mono_mass "1118.331939"
-xref: spec_1_neutral_loss_1119_avge_mass "1119.0112"
-xref: spec_1_neutral_loss_1119_flag "false"
-xref: spec_1_neutral_loss_1119_composition "O(3) S dHex Hex(3) HexNAc(2)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1119_mono_mass "1118.331939"
-xref: spec_2_neutral_loss_1119_avge_mass "1119.0112"
-xref: spec_2_neutral_loss_1119_flag "false"
-xref: spec_2_neutral_loss_1119_composition "O(3) S dHex Hex(3) HexNAc(2)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1765
-name: dHex(2)Hex(3)HexNAc(2)
-def: "DHex(2) Hex(3) HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=3&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1765]
-xref: record_id "1765"
-xref: delta_mono_mass "1184.433033"
-xref: delta_avge_mass "1185.0892"
-xref: delta_composition "dHex(2) Hex(3) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1185_mono_mass "1184.433033"
-xref: spec_1_neutral_loss_1185_avge_mass "1185.0892"
-xref: spec_1_neutral_loss_1185_flag "false"
-xref: spec_1_neutral_loss_1185_composition "dHex(2) Hex(3) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1185_mono_mass "1184.433033"
-xref: spec_1_neutral_loss_1185_avge_mass "1185.0892"
-xref: spec_1_neutral_loss_1185_flag "false"
-xref: spec_1_neutral_loss_1185_composition "dHex(2) Hex(3) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1185_mono_mass "1184.433033"
-xref: spec_2_neutral_loss_1185_avge_mass "1185.0892"
-xref: spec_2_neutral_loss_1185_flag "false"
-xref: spec_2_neutral_loss_1185_composition "dHex(2) Hex(3) HexNAc(2)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1766
-name: dHex(1)Hex(4)HexNAc(2)
-def: "DHex Hex(4) HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hexac=2&mode=exact, URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=4&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1766]
-xref: record_id "1766"
-xref: delta_mono_mass "1200.427948"
-xref: delta_avge_mass "1201.0886"
-xref: delta_composition "dHex(1) Hex(4) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1201_mono_mass "1200.427948"
-xref: spec_1_neutral_loss_1201_avge_mass "1201.0886"
-xref: spec_1_neutral_loss_1201_flag "false"
-xref: spec_1_neutral_loss_1201_composition "dHex(1) Hex(4) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1201_mono_mass "1200.427948"
-xref: spec_1_neutral_loss_1201_avge_mass "1201.0886"
-xref: spec_1_neutral_loss_1201_flag "false"
-xref: spec_1_neutral_loss_1201_composition "dHex(1) Hex(4) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1201_mono_mass "1200.427948"
-xref: spec_2_neutral_loss_1201_avge_mass "1201.0886"
-xref: spec_2_neutral_loss_1201_flag "false"
-xref: spec_2_neutral_loss_1201_composition "dHex(1) Hex(4) HexNAc(2)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1767
-name: dHex(2)Hex(2)HexNAc(3)
-def: "DHex(2) Hex(2) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=2&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1767]
-xref: record_id "1767"
-xref: delta_mono_mass "1225.459583"
-xref: delta_avge_mass "1226.1412"
-xref: delta_composition "dHex(2) Hex(2) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1226_mono_mass "1225.459583"
-xref: spec_1_neutral_loss_1226_avge_mass "1226.1412"
-xref: spec_1_neutral_loss_1226_flag "false"
-xref: spec_1_neutral_loss_1226_composition "dHex(2) Hex(2) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1226_mono_mass "1225.459583"
-xref: spec_1_neutral_loss_1226_avge_mass "1226.1412"
-xref: spec_1_neutral_loss_1226_flag "false"
-xref: spec_1_neutral_loss_1226_composition "dHex(2) Hex(2) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1226_mono_mass "1225.459583"
-xref: spec_2_neutral_loss_1226_avge_mass "1226.1412"
-xref: spec_2_neutral_loss_1226_flag "false"
-xref: spec_2_neutral_loss_1226_composition "dHex(2) Hex(2) HexNAc(3)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1768
-name: dHex(1)Hex(3)HexNAc(3)
-def: "DHex Hex(3) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1768]
-xref: record_id "1768"
-xref: delta_mono_mass "1241.454497"
-xref: delta_avge_mass "1242.1406"
-xref: delta_composition "dHex(1) Hex(3) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1242_mono_mass "1241.454497"
-xref: spec_1_neutral_loss_1242_avge_mass "1242.1406"
-xref: spec_1_neutral_loss_1242_flag "false"
-xref: spec_1_neutral_loss_1242_composition "dHex(1) Hex(3) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1242_mono_mass "1241.454497"
-xref: spec_1_neutral_loss_1242_avge_mass "1242.1406"
-xref: spec_1_neutral_loss_1242_flag "false"
-xref: spec_1_neutral_loss_1242_composition "dHex(1) Hex(3) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1242_mono_mass "1241.454497"
-xref: spec_2_neutral_loss_1242_avge_mass "1242.1406"
-xref: spec_2_neutral_loss_1242_flag "false"
-xref: spec_2_neutral_loss_1242_composition "dHex(1) Hex(3) HexNAc(3)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1769
-name: Hex(4)HexNAc(3)
-def: "Hex(4) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1769]
-xref: record_id "1769"
-xref: delta_mono_mass "1257.449412"
-xref: delta_avge_mass "1258.14"
-xref: delta_composition "Hex(4) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1258_mono_mass "1257.449412"
-xref: spec_1_neutral_loss_1258_avge_mass "1258.14"
-xref: spec_1_neutral_loss_1258_flag "false"
-xref: spec_1_neutral_loss_1258_composition "Hex(4) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1258_mono_mass "1257.449412"
-xref: spec_1_neutral_loss_1258_avge_mass "1258.14"
-xref: spec_1_neutral_loss_1258_flag "false"
-xref: spec_1_neutral_loss_1258_composition "Hex(4) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1258_mono_mass "1257.449412"
-xref: spec_2_neutral_loss_1258_avge_mass "1258.14"
-xref: spec_2_neutral_loss_1258_flag "false"
-xref: spec_2_neutral_loss_1258_composition "Hex(4) HexNAc(3)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1770
-name: dHex(2)Hex(4)HexNAc(2)
-def: "DHex(2) Hex(4) HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=4&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1770]
-xref: record_id "1770"
-xref: delta_mono_mass "1346.485857"
-xref: delta_avge_mass "1347.2298"
-xref: delta_composition "dHex(2) Hex(4) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1347_mono_mass "1346.485857"
-xref: spec_1_neutral_loss_1347_avge_mass "1347.2298"
-xref: spec_1_neutral_loss_1347_flag "false"
-xref: spec_1_neutral_loss_1347_composition "dHex(2) Hex(4) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1347_mono_mass "1346.485857"
-xref: spec_1_neutral_loss_1347_avge_mass "1347.2298"
-xref: spec_1_neutral_loss_1347_flag "false"
-xref: spec_1_neutral_loss_1347_composition "dHex(2) Hex(4) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1347_mono_mass "1346.485857"
-xref: spec_2_neutral_loss_1347_avge_mass "1347.2298"
-xref: spec_2_neutral_loss_1347_flag "false"
-xref: spec_2_neutral_loss_1347_composition "dHex(2) Hex(4) HexNAc(2)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1771
-name: dHex(2)Hex(3)HexNAc(3)
-def: "DHex(2) Hex(3) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=3&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1771]
-xref: record_id "1771"
-xref: delta_mono_mass "1387.512406"
-xref: delta_avge_mass "1388.2818"
-xref: delta_composition "dHex(2) Hex(3) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1388_mono_mass "1387.512406"
-xref: spec_1_neutral_loss_1388_avge_mass "1388.2818"
-xref: spec_1_neutral_loss_1388_flag "false"
-xref: spec_1_neutral_loss_1388_composition "dHex(2) Hex(3) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1388_mono_mass "1387.512406"
-xref: spec_1_neutral_loss_1388_avge_mass "1388.2818"
-xref: spec_1_neutral_loss_1388_flag "false"
-xref: spec_1_neutral_loss_1388_composition "dHex(2) Hex(3) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1388_mono_mass "1387.512406"
-xref: spec_2_neutral_loss_1388_avge_mass "1388.2818"
-xref: spec_2_neutral_loss_1388_flag "false"
-xref: spec_2_neutral_loss_1388_composition "dHex(2) Hex(3) HexNAc(3)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1772
-name: Hex(3)HexNAc(5)
-def: "A3." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1772]
-xref: record_id "1772"
-xref: delta_mono_mass "1501.555334"
-xref: delta_avge_mass "1502.3844"
-xref: delta_composition "Hex(3) HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2020-08-02 11:46:20"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1502_mono_mass "1501.555334"
-xref: spec_1_neutral_loss_1502_avge_mass "1502.3844"
-xref: spec_1_neutral_loss_1502_flag "false"
-xref: spec_1_neutral_loss_1502_composition "Hex(3) HexNAc(5)"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1502_mono_mass "1501.555334"
-xref: spec_1_neutral_loss_1502_avge_mass "1502.3844"
-xref: spec_1_neutral_loss_1502_flag "false"
-xref: spec_1_neutral_loss_1502_composition "Hex(3) HexNAc(5)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1502_mono_mass "1501.555334"
-xref: spec_2_neutral_loss_1502_avge_mass "1502.3844"
-xref: spec_2_neutral_loss_1502_flag "false"
-xref: spec_2_neutral_loss_1502_composition "Hex(3) HexNAc(5)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1773
-name: Hex(4)HexNAc(3)NeuAc(1)
-def: "Hex(4) HexNAc(3) NeuAc ---OR--- Hex(3) HexNAc(4) Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexnac=3&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1773]
-xref: record_id "1773"
-xref: delta_mono_mass "1548.544828"
-xref: delta_avge_mass "1549.3945"
-xref: delta_composition "Hex(4) HexNAc(3) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-17 15:42:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1549_mono_mass "1548.544828"
-xref: spec_1_neutral_loss_1549_avge_mass "1549.3945"
-xref: spec_1_neutral_loss_1549_flag "false"
-xref: spec_1_neutral_loss_1549_composition "Hex(4) HexNAc(3) NeuAc"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1549_mono_mass "1548.544828"
-xref: spec_1_neutral_loss_1549_avge_mass "1549.3945"
-xref: spec_1_neutral_loss_1549_flag "false"
-xref: spec_1_neutral_loss_1549_composition "Hex(4) HexNAc(3) NeuAc"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1549_mono_mass "1548.544828"
-xref: spec_2_neutral_loss_1549_avge_mass "1549.3945"
-xref: spec_2_neutral_loss_1549_flag "false"
-xref: spec_2_neutral_loss_1549_composition "Hex(4) HexNAc(3) NeuAc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1774
-name: dHex(2)Hex(3)HexNAc(4)
-def: "DHex(2) Hex(3) HexNAc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=3&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1774]
-xref: record_id "1774"
-xref: delta_mono_mass "1590.591779"
-xref: delta_avge_mass "1591.4743"
-xref: delta_composition "dHex(2) Hex(3) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1591_mono_mass "1590.591779"
-xref: spec_1_neutral_loss_1591_avge_mass "1591.4743"
-xref: spec_1_neutral_loss_1591_flag "false"
-xref: spec_1_neutral_loss_1591_composition "dHex(2) Hex(3) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1591_mono_mass "1590.591779"
-xref: spec_1_neutral_loss_1591_avge_mass "1591.4743"
-xref: spec_1_neutral_loss_1591_flag "false"
-xref: spec_1_neutral_loss_1591_composition "dHex(2) Hex(3) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1591_mono_mass "1590.591779"
-xref: spec_2_neutral_loss_1591_avge_mass "1591.4743"
-xref: spec_2_neutral_loss_1591_flag "false"
-xref: spec_2_neutral_loss_1591_composition "dHex(2) Hex(3) HexNAc(4)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1775
-name: dHex(1)Hex(3)HexNAc(5)
-def: "DHex Hex(3) HexNAc(5)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1775]
-xref: record_id "1775"
-xref: delta_mono_mass "1647.613242"
-xref: delta_avge_mass "1648.5256"
-xref: delta_composition "dHex(1) Hex(3) HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1648_mono_mass "1647.613242"
-xref: spec_1_neutral_loss_1648_avge_mass "1648.5256"
-xref: spec_1_neutral_loss_1648_flag "false"
-xref: spec_1_neutral_loss_1648_composition "dHex(1) Hex(3) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1648_mono_mass "1647.613242"
-xref: spec_1_neutral_loss_1648_avge_mass "1648.5256"
-xref: spec_1_neutral_loss_1648_flag "false"
-xref: spec_1_neutral_loss_1648_composition "dHex(1) Hex(3) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1648_mono_mass "1647.613242"
-xref: spec_2_neutral_loss_1648_avge_mass "1648.5256"
-xref: spec_2_neutral_loss_1648_flag "false"
-xref: spec_2_neutral_loss_1648_composition "dHex(1) Hex(3) HexNAc(5)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1776
-name: Hex(3)HexNAc(6)
-def: "A4." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=6&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1776]
-xref: record_id "1776"
-xref: delta_mono_mass "1704.634706"
-xref: delta_avge_mass "1705.5769"
-xref: delta_composition "Hex(3) HexNAc(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2020-08-02 11:48:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1705_mono_mass "1704.634706"
-xref: spec_1_neutral_loss_1705_avge_mass "1705.5769"
-xref: spec_1_neutral_loss_1705_flag "false"
-xref: spec_1_neutral_loss_1705_composition "Hex(3) HexNAc(6)"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1705_mono_mass "1704.634706"
-xref: spec_1_neutral_loss_1705_avge_mass "1705.5769"
-xref: spec_1_neutral_loss_1705_flag "false"
-xref: spec_1_neutral_loss_1705_composition "Hex(3) HexNAc(6)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1705_mono_mass "1704.634706"
-xref: spec_2_neutral_loss_1705_avge_mass "1705.5769"
-xref: spec_2_neutral_loss_1705_flag "false"
-xref: spec_2_neutral_loss_1705_composition "Hex(3) HexNAc(6)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1777
-name: Hex(4)HexNAc(4)NeuAc(1)
-def: "Hex(4) HexNAc(4) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexnac=4&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1777]
-xref: record_id "1777"
-xref: delta_mono_mass "1751.624201"
-xref: delta_avge_mass "1752.5871"
-xref: delta_composition "Hex(4) HexNAc(4) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1752_mono_mass "1751.624201"
-xref: spec_1_neutral_loss_1752_avge_mass "1752.5871"
-xref: spec_1_neutral_loss_1752_flag "false"
-xref: spec_1_neutral_loss_1752_composition "Hex(4) HexNAc(4) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1752_mono_mass "1751.624201"
-xref: spec_1_neutral_loss_1752_avge_mass "1752.5871"
-xref: spec_1_neutral_loss_1752_flag "false"
-xref: spec_1_neutral_loss_1752_composition "Hex(4) HexNAc(4) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1752_mono_mass "1751.624201"
-xref: spec_2_neutral_loss_1752_avge_mass "1752.5871"
-xref: spec_2_neutral_loss_1752_flag "false"
-xref: spec_2_neutral_loss_1752_composition "Hex(4) HexNAc(4) NeuAc(1)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1778
-name: dHex(2)Hex(4)HexNAc(4)
-def: "DHex(2) Hex(4) HexNAc(4) ---OR--- Hex(4) HexNAc(4) dHex Pent Me." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=4&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1778]
-xref: record_id "1778"
-xref: delta_mono_mass "1752.644602"
-xref: delta_avge_mass "1753.6149"
-xref: delta_composition "dHex(2) Hex(4) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-22 11:07:26"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1753_mono_mass "1752.644602"
-xref: spec_1_neutral_loss_1753_avge_mass "1753.6149"
-xref: spec_1_neutral_loss_1753_flag "false"
-xref: spec_1_neutral_loss_1753_composition "dHex(2) Hex(4) HexNAc(4)"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1753_mono_mass "1752.644602"
-xref: spec_1_neutral_loss_1753_avge_mass "1753.6149"
-xref: spec_1_neutral_loss_1753_flag "false"
-xref: spec_1_neutral_loss_1753_composition "dHex(2) Hex(4) HexNAc(4)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_1753_mono_mass "1752.644602"
-xref: spec_2_neutral_loss_1753_avge_mass "1753.6149"
-xref: spec_2_neutral_loss_1753_flag "false"
-xref: spec_2_neutral_loss_1753_composition "dHex(2) Hex(4) HexNAc(4)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1779
-name: Hex(6)HexNAc(4)
-def: "Hex(6) HexNAc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=6&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1779]
-xref: record_id "1779"
-xref: delta_mono_mass "1784.634431"
-xref: delta_avge_mass "1785.6137"
-xref: delta_composition "Hex(6) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1785_mono_mass "1784.634431"
-xref: spec_1_neutral_loss_1785_avge_mass "1785.6137"
-xref: spec_1_neutral_loss_1785_flag "false"
-xref: spec_1_neutral_loss_1785_composition "Hex(6) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1785_mono_mass "1784.634431"
-xref: spec_1_neutral_loss_1785_avge_mass "1785.6137"
-xref: spec_1_neutral_loss_1785_flag "false"
-xref: spec_1_neutral_loss_1785_composition "Hex(6) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1785_mono_mass "1784.634431"
-xref: spec_2_neutral_loss_1785_avge_mass "1785.6137"
-xref: spec_2_neutral_loss_1785_flag "false"
-xref: spec_2_neutral_loss_1785_composition "Hex(6) HexNAc(4)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1780
-name: Hex(5)HexNAc(5)
-def: "Hex(5) HexNAc(5)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=5&hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1780]
-xref: record_id "1780"
-xref: delta_mono_mass "1825.660981"
-xref: delta_avge_mass "1826.6656"
-xref: delta_composition "Hex(5) HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1826_mono_mass "1825.660981"
-xref: spec_1_neutral_loss_1826_avge_mass "1826.6656"
-xref: spec_1_neutral_loss_1826_flag "false"
-xref: spec_1_neutral_loss_1826_composition "Hex(5) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1826_mono_mass "1825.660981"
-xref: spec_1_neutral_loss_1826_avge_mass "1826.6656"
-xref: spec_1_neutral_loss_1826_flag "false"
-xref: spec_1_neutral_loss_1826_composition "Hex(5) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1826_mono_mass "1825.660981"
-xref: spec_2_neutral_loss_1826_avge_mass "1826.6656"
-xref: spec_2_neutral_loss_1826_flag "false"
-xref: spec_2_neutral_loss_1826_composition "Hex(5) HexNAc(5)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1781
-name: dHex(1)Hex(3)HexNAc(6)
-def: "DHex Hex(3) HexNAc(6)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexnac=6&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1781]
-xref: record_id "1781"
-xref: delta_mono_mass "1850.692615"
-xref: delta_avge_mass "1851.7181"
-xref: delta_composition "dHex(1) Hex(3) HexNAc(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1851_mono_mass "1850.692615"
-xref: spec_1_neutral_loss_1851_avge_mass "1851.7181"
-xref: spec_1_neutral_loss_1851_flag "false"
-xref: spec_1_neutral_loss_1851_composition "dHex(1) Hex(3) HexNAc(6)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1851_mono_mass "1850.692615"
-xref: spec_1_neutral_loss_1851_avge_mass "1851.7181"
-xref: spec_1_neutral_loss_1851_flag "false"
-xref: spec_1_neutral_loss_1851_composition "dHex(1) Hex(3) HexNAc(6)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1851_mono_mass "1850.692615"
-xref: spec_2_neutral_loss_1851_avge_mass "1851.7181"
-xref: spec_2_neutral_loss_1851_flag "false"
-xref: spec_2_neutral_loss_1851_composition "dHex(1) Hex(3) HexNAc(6)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1782
-name: dHex(1)Hex(4)HexNAc(4)NeuAc(1)
-def: "DHex Hex(4) HexNAc(4) NeuAc ---OR--- Hex(3) HexNAc(5) dHex Kdn." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=4&hexnac=4&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1782]
-xref: record_id "1782"
-xref: delta_mono_mass "1897.68211"
-xref: delta_avge_mass "1898.7283"
-xref: delta_composition "dHex Hex(4) HexNAc(4) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2017-11-22 11:17:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1898_mono_mass "1897.68211"
-xref: spec_1_neutral_loss_1898_avge_mass "1898.7283"
-xref: spec_1_neutral_loss_1898_flag "false"
-xref: spec_1_neutral_loss_1898_composition "dHex Hex(4) HexNAc(4) NeuAc"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1898_mono_mass "1897.68211"
-xref: spec_1_neutral_loss_1898_avge_mass "1898.7283"
-xref: spec_1_neutral_loss_1898_flag "false"
-xref: spec_1_neutral_loss_1898_composition "dHex Hex(4) HexNAc(4) NeuAc"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_1898_mono_mass "1897.68211"
-xref: spec_2_neutral_loss_1898_avge_mass "1898.7283"
-xref: spec_2_neutral_loss_1898_flag "false"
-xref: spec_2_neutral_loss_1898_composition "dHex Hex(4) HexNAc(4) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1783
-name: dHex(3)Hex(4)HexNAc(4)
-def: "DHex(3) Hex(4) HexNAc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=3&hex=4&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1783]
-xref: record_id "1783"
-xref: delta_mono_mass "1898.702511"
-xref: delta_avge_mass "1899.7561"
-xref: delta_composition "dHex(3) Hex(4) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1899_mono_mass "1898.702511"
-xref: spec_1_neutral_loss_1899_avge_mass "1899.7561"
-xref: spec_1_neutral_loss_1899_flag "false"
-xref: spec_1_neutral_loss_1899_composition "dHex(3) Hex(4) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1899_mono_mass "1898.702511"
-xref: spec_1_neutral_loss_1899_avge_mass "1899.7561"
-xref: spec_1_neutral_loss_1899_flag "false"
-xref: spec_1_neutral_loss_1899_composition "dHex(3) Hex(4) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1899_mono_mass "1898.702511"
-xref: spec_2_neutral_loss_1899_avge_mass "1899.7561"
-xref: spec_2_neutral_loss_1899_flag "false"
-xref: spec_2_neutral_loss_1899_composition "dHex(3) Hex(4) HexNAc(4)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1784
-name: dHex(1)Hex(3)HexNAc(5)NeuAc(1)
-def: "DHex Hex(3) HexNAc(5) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=3&hexnac=5&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1784]
-xref: record_id "1784"
-xref: delta_mono_mass "1938.708659"
-xref: delta_avge_mass "1939.7802"
-xref: delta_composition "dHex(1) Hex(3) HexNAc(5) NeuAc(1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1939_mono_mass "1938.708659"
-xref: spec_1_neutral_loss_1939_avge_mass "1939.7802"
-xref: spec_1_neutral_loss_1939_flag "false"
-xref: spec_1_neutral_loss_1939_composition "dHex(1) Hex(3) HexNAc(5) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1939_mono_mass "1938.708659"
-xref: spec_1_neutral_loss_1939_avge_mass "1939.7802"
-xref: spec_1_neutral_loss_1939_flag "false"
-xref: spec_1_neutral_loss_1939_composition "dHex(1) Hex(3) HexNAc(5) NeuAc(1)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1939_mono_mass "1938.708659"
-xref: spec_2_neutral_loss_1939_avge_mass "1939.7802"
-xref: spec_2_neutral_loss_1939_flag "false"
-xref: spec_2_neutral_loss_1939_composition "dHex(1) Hex(3) HexNAc(5) NeuAc(1)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1785
-name: dHex(2)Hex(4)HexNAc(5)
-def: "DHex(2) Hex(4) HexNAc(5)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=4&hexnac=5&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1785]
-xref: record_id "1785"
-xref: delta_mono_mass "1955.723975"
-xref: delta_avge_mass "1956.8074"
-xref: delta_composition "dHex(2) Hex(4) HexNAc(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 12:00:00"
-xref: date_time_modified "2015-05-05 12:00:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1956_mono_mass "1955.723975"
-xref: spec_1_neutral_loss_1956_avge_mass "1956.8074"
-xref: spec_1_neutral_loss_1956_flag "false"
-xref: spec_1_neutral_loss_1956_composition "dHex(2) Hex(4) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1956_mono_mass "1955.723975"
-xref: spec_1_neutral_loss_1956_avge_mass "1956.8074"
-xref: spec_1_neutral_loss_1956_flag "false"
-xref: spec_1_neutral_loss_1956_composition "dHex(2) Hex(4) HexNAc(5)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_1956_mono_mass "1955.723975"
-xref: spec_2_neutral_loss_1956_avge_mass "1956.8074"
-xref: spec_2_neutral_loss_1956_flag "false"
-xref: spec_2_neutral_loss_1956_composition "dHex(2) Hex(4) HexNAc(5)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1786
-name: Hex(1)HexNAc(1)NeuAc(1)Ac(1)
-def: "Ac Hex HexNAc NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?acetyl=1&hex=1&hexnac=1&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1786]
-xref: record_id "1786"
-xref: delta_mono_mass "698.238177"
-xref: delta_avge_mass "698.6244"
-xref: delta_composition "Ac Hex HexNAc NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-05 16:37:35"
-xref: date_time_modified "2015-05-06 09:37:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_699_mono_mass "698.238177"
-xref: spec_1_neutral_loss_699_avge_mass "698.6244"
-xref: spec_1_neutral_loss_699_flag "false"
-xref: spec_1_neutral_loss_699_composition "Ac Hex HexNAc NeuAc"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_699_mono_mass "698.238177"
-xref: spec_1_neutral_loss_699_avge_mass "698.6244"
-xref: spec_1_neutral_loss_699_flag "false"
-xref: spec_1_neutral_loss_699_composition "Ac Hex HexNAc NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1787
-name: Label:13C(2)15N(2)
-def: "13C(2) 15N(2)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1787]
-comment: For SILAC experiments.
-synonym: "K4" RELATED []
-xref: record_id "1787"
-xref: delta_mono_mass "4.00078"
-xref: delta_avge_mass "3.9721"
-xref: delta_composition "C(-2) 13C(2) N(-2) 15N(2)"
-xref: username_of_poster "rbomgard"
-xref: group_of_poster ""
-xref: date_time_posted "2015-05-15 22:30:48"
-xref: date_time_modified "2015-05-24 18:09:48"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1789
-name: Xlink:DSS[155]
-def: "Ammonium-quenched monolink of DSS/BS3 crosslinker." [PMID:8326953, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1789]
-xref: record_id "1789"
-xref: delta_mono_mass "155.094629"
-xref: delta_avge_mass "155.1943"
-xref: delta_composition "H(13) C(8) N O(2)"
-xref: username_of_poster "johant"
-xref: group_of_poster ""
-xref: date_time_posted "2015-06-17 14:35:50"
-xref: date_time_modified "2017-08-17 15:09:42"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1799
-name: NQIGG
-def: "SUMOylation by Giardia lamblia." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1799]
-xref: record_id "1799"
-xref: delta_mono_mass "469.228496"
-xref: delta_avge_mass "469.4921"
-xref: delta_composition "H(31) C(19) N(7) O(7)"
-xref: username_of_poster "brunog"
-xref: group_of_poster ""
-xref: date_time_posted "2015-10-02 16:16:32"
-xref: date_time_modified "2015-11-01 16:20:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1800
-name: Carboxyethylpyrrole
-def: "Carboxyethylpyrrole." [PMID:12923198, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1800]
-xref: record_id "1800"
-xref: delta_mono_mass "122.036779"
-xref: delta_avge_mass "122.1213"
-xref: delta_composition "H(6) C(7) O(2)"
-xref: username_of_poster "jsc17"
-xref: group_of_poster ""
-xref: date_time_posted "2015-11-19 01:35:22"
-xref: date_time_modified "2016-04-06 08:03:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1801
-name: Fluorescein-tyramine
-def: "Fluorescein-tyramine adduct by peroxidase activity." [URL:http\://www.biosyn.com/tew/tyramide-signal-amplification.aspx, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1801]
-xref: record_id "1801"
-xref: delta_mono_mass "493.116152"
-xref: delta_avge_mass "493.4637"
-xref: delta_composition "H(19) C(29) N O(7)"
-xref: username_of_poster "Hideaki"
-xref: group_of_poster ""
-xref: date_time_posted "2016-02-02 11:23:24"
-xref: date_time_modified "2016-04-06 08:08:06"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1824
-name: GEE
-def: "Transamidation of glycine ethyl ester to glutamine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1824]
-xref: record_id "1824"
-xref: delta_mono_mass "86.036779"
-xref: delta_avge_mass "86.0892"
-xref: delta_composition "H(6) C(4) O(2)"
-xref: username_of_poster "michaelmerchant"
-xref: group_of_poster ""
-xref: date_time_posted "2016-05-12 15:56:17"
-xref: date_time_modified "2016-05-18 17:11:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "GEE (glycine ethyl ester) is a substrate for the enzyme Factor XIII for cross-linking to fibrinogen"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1825
-name: RNPXL
-def: "Simulate peptide-RNA conjugates." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1825]
-xref: record_id "1825"
-xref: delta_mono_mass "324.035867"
-xref: delta_avge_mass "324.1813"
-xref: delta_composition "H(13) C(9) N(2) O(9) P"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2016-06-05 14:23:58"
-xref: date_time_modified "2016-07-01 11:23:46"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Other"
-xref: spec_1_neutral_loss_325_mono_mass "324.035867"
-xref: spec_1_neutral_loss_325_avge_mass "324.1813"
-xref: spec_1_neutral_loss_325_flag "false"
-xref: spec_1_neutral_loss_325_composition "H(13) C(9) N(2) O(9) P"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "R"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Other"
-xref: spec_2_neutral_loss_325_mono_mass "324.035867"
-xref: spec_2_neutral_loss_325_avge_mass "324.1813"
-xref: spec_2_neutral_loss_325_flag "false"
-xref: spec_2_neutral_loss_325_composition "H(13) C(9) N(2) O(9) P"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1826
-name: Glu->pyro-Glu+Methyl
-def: "Pyro-Glu from E + Methylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1826]
-xref: record_id "1826"
-xref: delta_mono_mass "-3.994915"
-xref: delta_avge_mass "-3.9887"
-xref: delta_composition "C O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2016-06-15 10:07:50"
-xref: date_time_modified "2016-06-15 10:07:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1827
-name: Glu->pyro-Glu+Methyl:2H(2)13C(1)
-def: "Pyro-Glu from E + Methylation Medium." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1827]
-xref: record_id "1827"
-xref: delta_mono_mass "-0.979006"
-xref: delta_avge_mass "-0.9837"
-xref: delta_composition "H(-2) 2H(2) 13C O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2016-06-15 10:30:37"
-xref: date_time_modified "2016-06-15 10:30:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1828
-name: LRGG+methyl
-def: "LeumethylArgGlyGly." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1828]
-comment: LRGG remnant of ubiquitin remaining attached to lysine with missed cleavage due to methylation of arginine.
-synonym: "LRGG ubiquitin remnant with methylated Arg" RELATED []
-xref: record_id "1828"
-xref: delta_mono_mass "397.243753"
-xref: delta_avge_mass "397.4725"
-xref: delta_composition "H(31) C(17) N(7) O(4)"
-xref: username_of_poster "bkatja"
-xref: group_of_poster ""
-xref: date_time_posted "2016-07-27 14:34:54"
-xref: date_time_modified "2016-09-23 13:43:32"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1829
-name: LRGG+dimethyl
-def: "LeudimethylArgGlyGly." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1829]
-comment: LRGG remnant of ubiquitin remaining attached to lysine with missed cleavage due to dimethylation of arginine.
-synonym: "LRGG ubiquitin remnant with dimethylated Arg" RELATED []
-xref: record_id "1829"
-xref: delta_mono_mass "411.259403"
-xref: delta_avge_mass "411.4991"
-xref: delta_composition "H(33) C(18) N(7) O(4)"
-xref: username_of_poster "bkatja"
-xref: group_of_poster ""
-xref: date_time_posted "2016-07-27 16:20:40"
-xref: date_time_modified "2016-09-23 13:43:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1830
-name: Biotin-tyramide
-def: "Biotin-Phenol." [PMID:29039416, URL:http\://www.iris-biotech.de/ls-3500, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1830]
-xref: record_id "1830"
-xref: delta_mono_mass "361.146012"
-xref: delta_avge_mass "361.4585"
-xref: delta_composition "H(23) C(18) N(3) O(3) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2016-08-04 08:05:43"
-xref: date_time_modified "2023-02-24 12:26:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_2_misc_notes "Only observed on a small fraction of residues (~2%). See doi: 10.1038/nmeth.4465"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "W"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_misc_notes "Only observed on a small fraction of residues (~2%). See doi: 10.1038/nmeth.4465"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1831
-name: Tris
-def: "Tris adduct causes 104 Da addition at asparagine-succinimide intermediate." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1831]
-synonym: "tris adduct at IgG causes 104 Da addition tris adduct at asparagine" RELATED []
-xref: record_id "1831"
-xref: delta_mono_mass "104.071154"
-xref: delta_avge_mass "104.1277"
-xref: delta_composition "H(10) C(4) N O(2)"
-xref: username_of_poster "pradeepnpraveen"
-xref: group_of_poster ""
-xref: date_time_posted "2016-08-04 12:54:25"
-xref: date_time_modified "2024-08-12 09:58:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_misc_notes "NG sequence specifically after deamidation - Deamidated Asparagine with adjacent glycine are prone for this modification."
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1832
-name: IASD
-def: "Iodoacetamide derivative of stilbene (reaction product with thiol)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1832]
-synonym: "4-acetamido-4'-((iodoacetyl)amino)stilbene-2,2'-disulfonic acid" RELATED []
-xref: record_id "1832"
-xref: delta_mono_mass "452.034807"
-xref: delta_avge_mass "452.4582"
-xref: delta_composition "H(16) C(18) N(2) O(8) S(2)"
-xref: username_of_poster "AberdeenProteomics"
-xref: group_of_poster ""
-xref: date_time_posted "2016-08-05 12:04:02"
-xref: date_time_modified "2016-09-23 13:49:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1833
-name: NP40
-def: "NP-40 synthetic polymer terminus." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1833]
-xref: record_id "1833"
-xref: delta_mono_mass "220.182715"
-xref: delta_avge_mass "220.3505"
-xref: delta_composition "H(24) C(15) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2016-08-22 14:48:48"
-xref: date_time_modified "2016-08-22 16:07:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1834
-name: Tween20
-def: "Tween 20 synthetic polymer terminus." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1834]
-xref: record_id "1834"
-xref: delta_mono_mass "165.164326"
-xref: delta_avge_mass "165.2951"
-xref: delta_composition "H(21) C(12)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2016-08-22 14:51:41"
-xref: date_time_modified "2016-08-22 16:07:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1835
-name: Tween80
-def: "Tween 80 synthetic polymer terminus." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1835]
-xref: record_id "1835"
-xref: delta_mono_mass "263.237491"
-xref: delta_avge_mass "263.4381"
-xref: delta_composition "H(31) C(18) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2016-08-22 14:52:52"
-xref: date_time_modified "2016-08-22 16:08:10"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Any C-term"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1836
-name: Triton
-def: "Triton synthetic polymer terminus." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1836]
-xref: record_id "1836"
-xref: delta_mono_mass "188.156501"
-xref: delta_avge_mass "188.3086"
-xref: delta_composition "H(20) C(14)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2016-08-22 14:53:44"
-xref: date_time_modified "2016-08-22 16:07:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Any C-term"
-xref: spec_1_classification "Other"
-xref: spec_1_misc_notes "Triton X-100"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Other"
-xref: spec_2_misc_notes "Triton X-114"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1837
-name: Brij35
-def: "Brij 35 synthetic polymer terminus." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1837]
-xref: record_id "1837"
-xref: delta_mono_mass "168.187801"
-xref: delta_avge_mass "168.319"
-xref: delta_composition "H(24) C(12)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2016-08-22 14:55:48"
-xref: date_time_modified "2016-08-22 16:07:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1838
-name: Brij58
-def: "Brij 58 synthetic polymer terminus." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1838]
-xref: record_id "1838"
-xref: delta_mono_mass "224.250401"
-xref: delta_avge_mass "224.4253"
-xref: delta_composition "H(32) C(16)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2016-08-22 14:56:22"
-xref: date_time_modified "2016-08-22 16:08:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1839
-name: betaFNA
-def: "Beta-Funaltrexamine." [PMID:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3523197/, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1839]
-comment: Covalently bound structure in Manglik et al., Fig. 1b-Fig1c. Chemical formula % Sigma catalog entry.
-xref: record_id "1839"
-xref: delta_mono_mass "454.210387"
-xref: delta_avge_mass "454.5155"
-xref: delta_composition "H(30) C(25) N(2) O(6)"
-xref: username_of_poster "shartson"
-xref: group_of_poster ""
-xref: date_time_posted "2016-08-26 19:59:17"
-xref: date_time_modified "2024-08-12 10:21:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1840
-name: dHex(1)Hex(7)HexNAc(4)
-def: "Fucosylated biantennary + 2 alphaGal." [PMID:http://www.ncbi.nlm.nih.gov/pubmed/23924801, URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=7&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1840]
-xref: record_id "1840"
-xref: delta_mono_mass "2092.745164"
-xref: delta_avge_mass "2093.8955"
-xref: delta_composition "dHex Hex(7) HexNAc(4)"
-xref: username_of_poster "suckau"
-xref: group_of_poster ""
-xref: date_time_posted "2016-09-05 15:52:53"
-xref: date_time_modified "2016-09-09 16:57:21"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_misc_notes "observed in monoclonal antibodies"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1841
-name: Biotin:Thermo-21328
-def: "EZ-Link Sulfo-NHS-SS-Biotin." [URL:https\://tools.thermofisher.com/content/sfs/manuals/MAN0011183_EZ_SulfoNHS_SS_Biotin_UG.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1841]
-synonym: "also Biotin:Thermo-21331" RELATED []
-xref: record_id "1841"
-xref: delta_mono_mass "389.090154"
-xref: delta_avge_mass "389.5564"
-xref: delta_composition "H(23) C(15) N(3) O(3) S(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2016-11-11 10:34:53"
-xref: date_time_modified "2016-11-11 10:36:26"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1843
-name: PhosphoCytidine
-def: "Cytidine monophosphate." [URL:dx.doi.org/10.1038/nchembio0609-378, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1843]
-comment: By analogy with AMP.
-synonym: "CMP" RELATED []
-xref: record_id "1843"
-xref: delta_mono_mass "305.041287"
-xref: delta_avge_mass "305.1812"
-xref: delta_composition "H(12) C(9) N(3) O(7) P"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-02-01 17:36:16"
-xref: date_time_modified "2017-02-02 10:16:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1845
-name: AzidoF
-def: "Azidophenylalanine." [PMID:26597962, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1845]
-xref: record_id "1845"
-xref: delta_mono_mass "41.001397"
-xref: delta_avge_mass "41.0122"
-xref: delta_composition "H(-1) N(3)"
-xref: username_of_poster "astridb"
-xref: group_of_poster ""
-xref: date_time_posted "2017-02-17 09:53:27"
-xref: date_time_modified "2017-03-03 15:46:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1846
-name: Dimethylaminoethyl
-def: "Cys alkylation by dimethylaminoethyl halide." [PMID:20373501, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1846]
-xref: record_id "1846"
-xref: delta_mono_mass "71.073499"
-xref: delta_avge_mass "71.121"
-xref: delta_composition "H(9) C(4) N"
-xref: username_of_poster "Kramerh"
-xref: group_of_poster ""
-xref: date_time_posted "2017-02-17 16:10:59"
-xref: date_time_modified "2017-03-03 15:50:09"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1848
-name: Gluratylation
-def: "Glutarylation." [PMID:24703693, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1848]
-xref: record_id "1848"
-xref: delta_mono_mass "114.031694"
-xref: delta_avge_mass "114.0993"
-xref: delta_composition "H(6) C(5) O(3)"
-xref: username_of_poster "cfeller"
-xref: group_of_poster ""
-xref: date_time_posted "2017-03-30 11:15:26"
-xref: date_time_modified "2017-04-05 12:31:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1849
-name: hydroxyisobutyryl
-def: "2-hydroxyisobutyrylation." [PMID:24681537, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1849]
-synonym: "2-hydroxyisobutanoyl 3-hydroxybutanoyl" RELATED []
-xref: record_id "1849"
-xref: delta_mono_mass "86.036779"
-xref: delta_avge_mass "86.0892"
-xref: delta_composition "H(6) C(4) O(2)"
-xref: username_of_poster "cfeller"
-xref: group_of_poster ""
-xref: date_time_posted "2017-03-30 11:16:14"
-xref: date_time_modified "2021-03-11 11:57:59"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1868
-name: MeMePhosphorothioate
-def: "S-Methyl Methyl phosphorothioate." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1868]
-xref: record_id "1868"
-xref: delta_mono_mass "107.979873"
-xref: delta_avge_mass "108.0993"
-xref: delta_composition "H(5) C(2) O P S"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2017-04-11 18:32:43"
-xref: date_time_modified "2017-06-02 16:01:58"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1870
-name: Cation:Fe[III]
-def: "Replacement of 3 protons by iron." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1870]
-xref: record_id "1870"
-xref: delta_mono_mass "52.911464"
-xref: delta_avge_mass "52.8212"
-xref: delta_composition "H(-3) Fe"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-06-15 12:58:58"
-xref: date_time_modified "2024-08-12 09:58:26"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1871
-name: DTT
-def: "DTT adduct of cysteine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1871]
-xref: record_id "1871"
-xref: delta_mono_mass "151.996571"
-xref: delta_avge_mass "152.2351"
-xref: delta_composition "H(8) C(4) O(2) S(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-06-15 14:09:46"
-xref: date_time_modified "2024-08-12 09:58:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1872
-name: DYn-2
-def: "Sulfenic Acid specific probe." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1872]
-xref: record_id "1872"
-xref: delta_mono_mass "161.09664"
-xref: delta_avge_mass "161.2203"
-xref: delta_composition "H(13) C(11) O"
-xref: username_of_poster "SamanthaLapehn"
-xref: group_of_poster ""
-xref: date_time_posted "2017-07-06 17:23:58"
-xref: date_time_modified "2017-08-05 02:16:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_1_misc_notes "-SOH"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1873
-name: MesitylOxide
-def: "Acetone chemical artifact." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1873]
-xref: record_id "1873"
-xref: delta_mono_mass "98.073165"
-xref: delta_avge_mass "98.143"
-xref: delta_composition "H(10) C(6) O"
-xref: username_of_poster "mlefers"
-xref: group_of_poster ""
-xref: date_time_posted "2017-07-13 19:50:51"
-xref: date_time_modified "2017-08-04 17:22:43"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1875
-name: methylol
-def: "Formaldehyde induced modifications." [PMID:https://www.ncbi.nlm.nih.gov/pubmed/16704222, PMID:https://www.ncbi.nlm.nih.gov/pubmed/14638685, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1875]
-xref: record_id "1875"
-xref: delta_mono_mass "30.010565"
-xref: delta_avge_mass "30.026"
-xref: delta_composition "H(2) C O"
-xref: username_of_poster "robertyen"
-xref: group_of_poster ""
-xref: date_time_posted "2017-07-14 18:43:02"
-xref: date_time_modified "2017-08-04 17:27:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "W"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1877
-name: Xlink:DSS[259]
-def: "Tris-quenched monolink of DSS/BS3 crosslinker." [PMID:8326953, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1877]
-xref: record_id "1877"
-xref: delta_mono_mass "259.141973"
-xref: delta_avge_mass "259.2988"
-xref: delta_composition "H(21) C(12) N O(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-17 14:29:30"
-xref: date_time_modified "2017-08-17 15:09:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1878
-name: Xlink:DSSO[176]
-def: "Water-quenched monolink of DSSO crosslinker." [URL:https\://www.thermofisher.com/order/catalog/product/A33545, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1878]
-xref: record_id "1878"
-xref: delta_mono_mass "176.01433"
-xref: delta_avge_mass "176.1903"
-xref: delta_composition "H(8) C(6) O(4) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-17 16:26:01"
-xref: date_time_modified "2017-08-17 16:26:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1879
-name: Xlink:DSSO[175]
-def: "Ammonia-quenched monolink of DSSO crosslinker." [URL:https\://www.thermofisher.com/order/catalog/product/A33545, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1879]
-xref: record_id "1879"
-xref: delta_mono_mass "175.030314"
-xref: delta_avge_mass "175.2056"
-xref: delta_composition "H(9) C(6) N O(3) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-17 16:27:45"
-xref: date_time_modified "2017-08-17 16:27:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1880
-name: Xlink:DSSO[279]
-def: "Tris-quenched monolink of DSSO crosslinker." [URL:https\://www.thermofisher.com/order/catalog/product/A33545, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1880]
-xref: record_id "1880"
-xref: delta_mono_mass "279.077658"
-xref: delta_avge_mass "279.3101"
-xref: delta_composition "H(17) C(10) N O(6) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-17 16:29:08"
-xref: date_time_modified "2017-08-17 16:29:08"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1881
-name: Xlink:DSSO[54]
-def: "Alkene fragment of DSSO crosslinker." [URL:https\://www.thermofisher.com/order/catalog/product/A33545, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1881]
-xref: record_id "1881"
-xref: delta_mono_mass "54.010565"
-xref: delta_avge_mass "54.0474"
-xref: delta_composition "H(2) C(3) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-17 16:31:03"
-xref: date_time_modified "2017-08-17 16:31:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1882
-name: Xlink:DSSO[86]
-def: "Thiol fragment of DSSO crosslinker." [URL:https\://www.thermofisher.com/order/catalog/product/A33545, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1882]
-xref: record_id "1882"
-xref: delta_mono_mass "85.982635"
-xref: delta_avge_mass "86.1124"
-xref: delta_composition "H(2) C(3) O S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-17 16:32:17"
-xref: date_time_modified "2017-08-17 16:32:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1883
-name: Xlink:DSSO[104]
-def: "Sulfenic acid fragment of DSSO crosslinker." [URL:https\://www.thermofisher.com/order/catalog/product/A33545, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1883]
-xref: record_id "1883"
-xref: delta_mono_mass "103.9932"
-xref: delta_avge_mass "104.1277"
-xref: delta_composition "H(4) C(3) O(2) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-17 16:33:16"
-xref: date_time_modified "2017-08-17 16:33:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1885
-name: Xlink:BuUrBu[111]
-def: "BuUr fragment of BuUrBu crosslinker." [URL:https\://www.thermofisher.com/order/catalog/product/A35459, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1885]
-xref: record_id "1885"
-xref: delta_mono_mass "111.032028"
-xref: delta_avge_mass "111.0987"
-xref: delta_composition "H(5) C(5) N O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-18 09:34:59"
-xref: date_time_modified "2024-08-12 10:24:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "S"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1886
-name: Xlink:BuUrBu[85]
-def: "Bu fragment of BuUrBu crosslinker." [URL:https\://www.thermofisher.com/order/catalog/product/A35459, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1886]
-xref: record_id "1886"
-xref: delta_mono_mass "85.052764"
-xref: delta_avge_mass "85.1045"
-xref: delta_composition "H(7) C(4) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-18 09:36:27"
-xref: date_time_modified "2024-08-12 10:23:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "S"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1887
-name: Xlink:BuUrBu[213]
-def: "Ammonia quenched monolink of BuUrBu crosslinker." [URL:https\://www.thermofisher.com/order/catalog/product/A35459, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1887]
-xref: record_id "1887"
-xref: delta_mono_mass "213.111341"
-xref: delta_avge_mass "213.2337"
-xref: delta_composition "H(15) C(9) N(3) O(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-18 09:38:52"
-xref: date_time_modified "2024-08-12 10:23:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "S"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1888
-name: Xlink:BuUrBu[214]
-def: "Water quenched monolink of BuUrBu crosslinker." [URL:https\://www.thermofisher.com/order/catalog/product/A35459, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1888]
-xref: record_id "1888"
-xref: delta_mono_mass "214.095357"
-xref: delta_avge_mass "214.2185"
-xref: delta_composition "H(14) C(9) N(2) O(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-18 09:43:05"
-xref: date_time_modified "2024-08-12 10:23:14"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "S"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1889
-name: Xlink:BuUrBu[317]
-def: "Tris quenched monolink of BuUrBu crosslinker." [URL:https\://www.thermofisher.com/order/catalog/product/A35459, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1889]
-xref: record_id "1889"
-xref: delta_mono_mass "317.158686"
-xref: delta_avge_mass "317.3382"
-xref: delta_composition "H(23) C(13) N(3) O(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-18 09:44:40"
-xref: date_time_modified "2024-08-12 10:22:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "S"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1896
-name: Xlink:DSSO[158]
-def: "Intact DSSO crosslinker." [URL:https\://www.thermofisher.com/order/catalog/product/A33545, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1896]
-xref: record_id "1896"
-xref: delta_mono_mass "158.003765"
-xref: delta_avge_mass "158.175"
-xref: delta_composition "H(6) C(6) O(3) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-31 14:53:02"
-xref: date_time_modified "2017-08-31 14:53:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1897
-name: Xlink:EGS[226]
-def: "Intact EGS cross-linker." [PMID:36892, URL:https\://tools.thermofisher.com/content/sfs/manuals/MAN0011281_EGS_SulfoEGS_UG.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1897]
-synonym: "Ethylene glycolbis(succinimidylsuccinate)" RELATED []
-xref: record_id "1897"
-xref: delta_mono_mass "226.047738"
-xref: delta_avge_mass "226.1828"
-xref: delta_composition "H(10) C(10) O(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-31 14:54:57"
-xref: date_time_modified "2017-08-31 14:54:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1898
-name: Xlink:DSS[138]
-def: "Intact DSS/BS3 crosslinker." [PMID:8326953, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1898]
-xref: record_id "1898"
-xref: delta_mono_mass "138.06808"
-xref: delta_avge_mass "138.1638"
-xref: delta_composition "H(10) C(8) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-31 14:55:56"
-xref: date_time_modified "2017-08-31 14:55:56"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1899
-name: Xlink:BuUrBu[196]
-def: "Intact BuUrBu crosslinker." [URL:https\://www.thermofisher.com/order/catalog/product/A35459, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1899]
-xref: record_id "1899"
-xref: delta_mono_mass "196.084792"
-xref: delta_avge_mass "196.2032"
-xref: delta_composition "H(12) C(9) N(2) O(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-31 14:57:02"
-xref: date_time_modified "2024-08-12 10:22:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "S"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1900
-name: Xlink:DTBP[172]
-def: "Intact DTBP crosslinker." [PMID:770170, URL:http\://tools.thermofisher.com/content/sfs/manuals/MAN0011314_ImidoesterCrsLnk_DMA_DMP_DMS_DTBP_UG.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1900]
-comment: Imidoester cross-linker.
-synonym: "dimethyl 3,3'-dithiobispropionimidate" RELATED []
-xref: record_id "1900"
-xref: delta_mono_mass "172.01289"
-xref: delta_avge_mass "172.2711"
-xref: delta_composition "H(8) C(6) N(2) S(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-31 14:59:08"
-xref: date_time_modified "2017-08-31 14:59:08"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1901
-name: Xlink:DST[114]
-def: "Intact DST crosslinker." [PMID:212103, URL:https\://assets.thermofisher.com/TFS-Assets/LSG/manuals/MAN0011282_DST_UG.pdf, PMID:3001048, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1901]
-xref: record_id "1901"
-xref: delta_mono_mass "113.995309"
-xref: delta_avge_mass "114.0563"
-xref: delta_composition "H(2) C(4) O(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-31 15:00:13"
-xref: date_time_modified "2017-08-31 15:00:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1902
-name: Xlink:DTSSP[174]
-def: "Intact DSP/DTSSP crosslinker." [URL:https\://tools.thermofisher.com/content/sfs/manuals/MAN0011280_DTSSP_DSP_UG.pdf, PMID:1262347, PMID:8457554, PMID:322714, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1902]
-synonym: "Also known as DSP" RELATED []
-xref: record_id "1902"
-xref: delta_mono_mass "173.980921"
-xref: delta_avge_mass "174.2406"
-xref: delta_composition "H(6) C(6) O(2) S(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-31 15:01:08"
-xref: date_time_modified "2017-08-31 15:01:08"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1903
-name: Xlink:SMCC[219]
-def: "Intact SMCC cross-link." [URL:https\://assets.thermofisher.com/TFS-Assets/LSG/manuals/MAN0011295_SMCC_SulfoSMCC_UG.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1903]
-xref: record_id "1903"
-xref: delta_mono_mass "219.089543"
-xref: delta_avge_mass "219.2365"
-xref: delta_composition "H(13) C(12) N O(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-08-31 15:02:14"
-xref: date_time_modified "2017-09-05 15:00:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1905
-name: Xlink:BS2G[96]
-def: "Intact BS2-G crosslinker." [URL:https\://assets.thermofisher.com/TFS-Assets/LSG/manuals/MAN0011542_BS3_d0d4_BS2G_d0d3_UG.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1905]
-xref: record_id "1905"
-xref: delta_mono_mass "96.021129"
-xref: delta_avge_mass "96.0841"
-xref: delta_composition "H(4) C(5) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-09-05 16:22:19"
-xref: date_time_modified "2017-09-05 16:22:37"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1906
-name: Xlink:BS2G[113]
-def: "Ammonium-quenched monolink of BS2-G crosslinker." [URL:https\://assets.thermofisher.com/TFS-Assets/LSG/manuals/MAN0011542_BS3_d0d4_BS2G_d0d3_UG.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1906]
-xref: record_id "1906"
-xref: delta_mono_mass "113.047679"
-xref: delta_avge_mass "113.1146"
-xref: delta_composition "H(7) C(5) N O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-09-05 16:26:19"
-xref: date_time_modified "2017-09-05 16:26:36"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1907
-name: Xlink:BS2G[114]
-def: "Water-quenched monolink of BS2-G crosslinker." [URL:https\://assets.thermofisher.com/TFS-Assets/LSG/manuals/MAN0011542_BS3_d0d4_BS2G_d0d3_UG.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1907]
-xref: record_id "1907"
-xref: delta_mono_mass "114.031694"
-xref: delta_avge_mass "114.0993"
-xref: delta_composition "H(6) C(5) O(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-09-05 16:27:03"
-xref: date_time_modified "2017-09-05 16:27:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1908
-name: Xlink:BS2G[217]
-def: "Tris-quenched monolink of BS2-G crosslinker." [URL:https\://assets.thermofisher.com/TFS-Assets/LSG/manuals/MAN0011542_BS3_d0d4_BS2G_d0d3_UG.pdf, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1908]
-xref: record_id "1908"
-xref: delta_mono_mass "217.095023"
-xref: delta_avge_mass "217.2191"
-xref: delta_composition "H(15) C(9) N O(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-09-05 16:28:28"
-xref: date_time_modified "2017-09-05 16:28:43"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1910
-name: Cation:Al[III]
-def: "Replacement of 3 protons by aluminium." [URL:http\://www.matrixscience.com/blog/trying-to-illuminate-proteomics-dark-matter.html, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1910]
-xref: record_id "1910"
-xref: delta_mono_mass "23.958063"
-xref: delta_avge_mass "23.9577"
-xref: delta_composition "H(-3) Al"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-09-05 17:13:59"
-xref: date_time_modified "2017-09-05 17:13:59"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1911
-name: Xlink:DMP[139]
-def: "Ammonia quenched monolink of DMP crosslinker." [PMID:2144419, PMID:14696200, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1911]
-synonym: "Dimethyl pimelimidate dead-end crosslink" RELATED []
-xref: record_id "1911"
-xref: delta_mono_mass "139.110947"
-xref: delta_avge_mass "139.1982"
-xref: delta_composition "H(13) C(7) N(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-09-06 10:03:30"
-xref: date_time_modified "2017-09-06 10:03:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1912
-name: Xlink:DMP[122]
-def: "Intact DMP crosslinker." [PMID:2144419, PMID:14696200, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1912]
-synonym: "Dimethyl pimelimidate" RELATED []
-xref: record_id "1912"
-xref: delta_mono_mass "122.084398"
-xref: delta_avge_mass "122.1677"
-xref: delta_composition "H(10) C(7) N(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-09-06 10:04:39"
-xref: date_time_modified "2017-09-06 10:04:39"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1913
-name: glyoxalAGE
-def: "Glyoxal-derived AGE." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1913]
-xref: record_id "1913"
-xref: delta_mono_mass "21.98435"
-xref: delta_avge_mass "22.0055"
-xref: delta_composition "H(-2) C(2)"
-xref: username_of_poster "mlefers"
-xref: group_of_poster ""
-xref: date_time_posted "2017-10-05 13:54:48"
-xref: date_time_modified "2017-11-08 17:25:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1914
-name: Met->AspSA
-def: "Methionine oxidation to aspartic semialdehyde." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1914]
-xref: record_id "1914"
-xref: delta_mono_mass "-32.008456"
-xref: delta_avge_mass "-32.1081"
-xref: delta_composition "H(-4) C(-1) O S(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-10-06 15:35:18"
-xref: date_time_modified "2017-10-06 15:37:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1915
-name: Decarboxylation
-def: "Decarboxylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1915]
-xref: record_id "1915"
-xref: delta_mono_mass "-30.010565"
-xref: delta_avge_mass "-30.026"
-xref: delta_composition "H(-2) C(-1) O(-1)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-10-06 15:40:31"
-xref: date_time_modified "2017-10-06 15:40:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "E"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1916
-name: Aspartylurea
-def: "Aspartylurea." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1916]
-xref: record_id "1916"
-xref: delta_mono_mass "-10.031969"
-xref: delta_avge_mass "-10.0412"
-xref: delta_composition "H(-2) C(-1) N(-2) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-10-06 15:43:52"
-xref: date_time_modified "2017-10-06 15:43:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1917
-name: Formylasparagine
-def: "In Bachi as Formylaspargine (typo?)." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1917]
-xref: record_id "1917"
-xref: delta_mono_mass "4.97893"
-xref: delta_avge_mass "4.9735"
-xref: delta_composition "H(-1) C(-1) N(-1) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-10-06 16:01:29"
-xref: date_time_modified "2017-11-02 17:23:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1918
-name: Carbonyl
-def: "Aldehyde and ketone modifications." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1918]
-xref: record_id "1918"
-xref: delta_mono_mass "13.979265"
-xref: delta_avge_mass "13.9835"
-xref: delta_composition "H(-2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-10-06 16:09:53"
-xref: date_time_modified "2017-10-06 16:12:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "A"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "E"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "I"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "L"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "Q"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "R"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "S"
-xref: spec_7_position "Anywhere"
-xref: spec_7_classification "Chemical derivative"
-xref: spec_8_group "8"
-xref: spec_8_hidden "1"
-xref: spec_8_site "V"
-xref: spec_8_position "Anywhere"
-xref: spec_8_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1920
-name: AFB1_Dialdehyde
-def: "Adduction of aflatoxin B1 Dialdehyde to lysine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1920]
-xref: record_id "1920"
-xref: delta_mono_mass "310.047738"
-xref: delta_avge_mass "310.2577"
-xref: delta_composition "H(10) C(17) O(6)"
-xref: username_of_poster "shenmic"
-xref: group_of_poster ""
-xref: date_time_posted "2017-10-17 14:58:16"
-xref: date_time_modified "2024-08-12 09:57:33"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1922
-name: Pro->HAVA
-def: "Proline oxidation to 5-hydroxy-2-aminovaleric acid." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1922]
-xref: record_id "1922"
-xref: delta_mono_mass "18.010565"
-xref: delta_avge_mass "18.0153"
-xref: delta_composition "H(2) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-03 09:13:16"
-xref: date_time_modified "2017-11-03 09:13:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "P"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1923
-name: Delta:H(-4)O(2)
-def: "Tryptophan oxidation to beta-unsaturated-2,4-bis-tryptophandione." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1923]
-xref: record_id "1923"
-xref: delta_mono_mass "27.958529"
-xref: delta_avge_mass "27.967"
-xref: delta_composition "H(-4) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-03 09:17:12"
-xref: date_time_modified "2017-11-08 17:00:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1924
-name: Delta:H(-4)O(3)
-def: "Tryptophan oxidation to hydroxy-bis-tryptophandione." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1924]
-xref: record_id "1924"
-xref: delta_mono_mass "43.953444"
-xref: delta_avge_mass "43.9664"
-xref: delta_composition "H(-4) O(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-08 16:11:21"
-xref: date_time_modified "2017-11-08 17:01:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1925
-name: Delta:O(4)
-def: "Tryptophan oxidation to dihydroxy-N-formaylkynurenine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1925]
-xref: record_id "1925"
-xref: delta_mono_mass "63.979659"
-xref: delta_avge_mass "63.9976"
-xref: delta_composition "O(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-08 16:33:11"
-xref: date_time_modified "2017-11-08 17:01:29"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1926
-name: Delta:H(4)C(3)O(2)
-def: "Methylglyoxal-derived carboxyethyllysine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1926]
-xref: record_id "1926"
-xref: delta_mono_mass "72.021129"
-xref: delta_avge_mass "72.0627"
-xref: delta_composition "H(4) C(3) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-08 16:41:02"
-xref: date_time_modified "2021-06-30 11:32:08"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_misc_notes "Note that Table 3 in the reference has the delta as H(3) C(3) O(2) = 71 Da"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1927
-name: Delta:H(4)C(5)O(1)
-def: "Methylglyoxal-derived argpyrimidine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1927]
-xref: record_id "1927"
-xref: delta_mono_mass "80.026215"
-xref: delta_avge_mass "80.0847"
-xref: delta_composition "H(4) C(5) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-08 16:43:41"
-xref: date_time_modified "2018-06-26 10:38:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1928
-name: Delta:H(10)C(8)O(1)
-def: "Crotonaldehyde-derived dimethyl-FDP-lysine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1928]
-xref: record_id "1928"
-xref: delta_mono_mass "122.073165"
-xref: delta_avge_mass "122.1644"
-xref: delta_composition "H(10) C(8) O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-08 17:04:01"
-xref: date_time_modified "2017-11-08 17:04:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1929
-name: Delta:H(6)C(7)O(4)
-def: "Methylglyoxal-derived tetrahydropyrimidine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1929]
-xref: record_id "1929"
-xref: delta_mono_mass "154.026609"
-xref: delta_avge_mass "154.1201"
-xref: delta_composition "H(6) C(7) O(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-08 17:12:02"
-xref: date_time_modified "2017-11-08 17:12:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "R"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1930
-name: Pent(2)
-def: "Pent(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?pent=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1930]
-xref: record_id "1930"
-xref: delta_mono_mass "264.084518"
-xref: delta_avge_mass "264.2292"
-xref: delta_composition "Pent(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-23 12:05:50"
-xref: date_time_modified "2017-11-23 13:01:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_265_mono_mass "264.084518"
-xref: spec_1_neutral_loss_265_avge_mass "264.2292"
-xref: spec_1_neutral_loss_265_flag "false"
-xref: spec_1_neutral_loss_265_composition "Pent(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_265_mono_mass "264.084518"
-xref: spec_1_neutral_loss_265_avge_mass "264.2292"
-xref: spec_1_neutral_loss_265_flag "false"
-xref: spec_1_neutral_loss_265_composition "Pent(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1931
-name: Pent(1)HexNAc(1)
-def: "Pent HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?pent=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1931]
-xref: record_id "1931"
-xref: delta_mono_mass "335.121631"
-xref: delta_avge_mass "335.3071"
-xref: delta_composition "Pent HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-23 13:00:37"
-xref: date_time_modified "2017-11-23 13:05:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_336_mono_mass "335.121631"
-xref: spec_1_neutral_loss_336_avge_mass "335.3071"
-xref: spec_1_neutral_loss_336_flag "false"
-xref: spec_1_neutral_loss_336_composition "Pent HexNAc"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_336_mono_mass "335.121631"
-xref: spec_1_neutral_loss_336_avge_mass "335.3071"
-xref: spec_1_neutral_loss_336_flag "false"
-xref: spec_1_neutral_loss_336_composition "Pent HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1932
-name: Hex(2)Sulf(1)
-def: "Hex(2) O(3) S." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hex=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1932]
-xref: record_id "1932"
-xref: delta_mono_mass "404.062462"
-xref: delta_avge_mass "404.3444"
-xref: delta_composition "O(3) S Hex(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-23 15:39:42"
-xref: date_time_modified "2017-11-23 15:40:36"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_405_mono_mass "404.062462"
-xref: spec_1_neutral_loss_405_avge_mass "404.3444"
-xref: spec_1_neutral_loss_405_flag "false"
-xref: spec_1_neutral_loss_405_composition "O(3) S Hex(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_405_mono_mass "404.062462"
-xref: spec_1_neutral_loss_405_avge_mass "404.3444"
-xref: spec_1_neutral_loss_405_flag "false"
-xref: spec_1_neutral_loss_405_composition "O(3) S Hex(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1933
-name: Hex(1)Pent(2)Me(1)
-def: "Hex:1 Pent:2 Me:1." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?methyl=1&pent=2&hex=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1933]
-xref: record_id "1933"
-xref: delta_mono_mass "440.152991"
-xref: delta_avge_mass "440.3964"
-xref: delta_composition "Me Pent(2) Hex"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-23 15:47:22"
-xref: date_time_modified "2017-11-23 15:49:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_441_mono_mass "440.152991"
-xref: spec_1_neutral_loss_441_avge_mass "440.3964"
-xref: spec_1_neutral_loss_441_flag "false"
-xref: spec_1_neutral_loss_441_composition "Me Pent(2) Hex"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_441_mono_mass "440.152991"
-xref: spec_1_neutral_loss_441_avge_mass "440.3964"
-xref: spec_1_neutral_loss_441_flag "false"
-xref: spec_1_neutral_loss_441_composition "Me Pent(2) Hex"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1934
-name: HexNAc(2)Sulf(1)
-def: "HexNAc(2) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1934]
-xref: record_id "1934"
-xref: delta_mono_mass "486.11556"
-xref: delta_avge_mass "486.4482"
-xref: delta_composition "O(3) S HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-23 16:35:09"
-xref: date_time_modified "2017-11-23 16:35:09"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_487_mono_mass "486.11556"
-xref: spec_1_neutral_loss_487_avge_mass "486.4482"
-xref: spec_1_neutral_loss_487_flag "false"
-xref: spec_1_neutral_loss_487_composition "O(3) S HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_487_mono_mass "486.11556"
-xref: spec_1_neutral_loss_487_avge_mass "486.4482"
-xref: spec_1_neutral_loss_487_flag "false"
-xref: spec_1_neutral_loss_487_composition "O(3) S HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1935
-name: Hex(1)Pent(3)Me(1)
-def: "Hex Pent(3) Me." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?methyl=1&pent=3&hex=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1935]
-xref: record_id "1935"
-xref: delta_mono_mass "572.19525"
-xref: delta_avge_mass "572.511"
-xref: delta_composition "Me Pent(3) Hex"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-23 16:40:05"
-xref: date_time_modified "2017-11-23 16:40:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_573_mono_mass "572.19525"
-xref: spec_1_neutral_loss_573_avge_mass "572.511"
-xref: spec_1_neutral_loss_573_flag "false"
-xref: spec_1_neutral_loss_573_composition "Me Pent(3) Hex"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_573_mono_mass "572.19525"
-xref: spec_1_neutral_loss_573_avge_mass "572.511"
-xref: spec_1_neutral_loss_573_flag "false"
-xref: spec_1_neutral_loss_573_composition "Me Pent(3) Hex"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1936
-name: Hex(2)Pent(2)
-def: "Hex(2) Pent(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?pent=2&hex=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1936]
-xref: record_id "1936"
-xref: delta_mono_mass "588.190165"
-xref: delta_avge_mass "588.5104"
-xref: delta_composition "Pent(2) Hex(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-23 17:22:55"
-xref: date_time_modified "2017-11-23 17:22:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_589_mono_mass "588.190165"
-xref: spec_1_neutral_loss_589_avge_mass "588.5104"
-xref: spec_1_neutral_loss_589_flag "false"
-xref: spec_1_neutral_loss_589_composition "Pent(2) Hex(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_589_mono_mass "588.190165"
-xref: spec_1_neutral_loss_589_avge_mass "588.5104"
-xref: spec_1_neutral_loss_589_flag "false"
-xref: spec_1_neutral_loss_589_composition "Pent(2) Hex(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1937
-name: Hex(2)Pent(2)Me(1)
-def: "Hex(2) Pent(2) Me." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?methyl=1&pent=2&hex=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1937]
-xref: record_id "1937"
-xref: delta_mono_mass "602.205815"
-xref: delta_avge_mass "602.537"
-xref: delta_composition "Me Pent(2) Hex(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-23 17:24:00"
-xref: date_time_modified "2017-11-23 17:24:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_603_mono_mass "602.205815"
-xref: spec_1_neutral_loss_603_avge_mass "602.537"
-xref: spec_1_neutral_loss_603_flag "false"
-xref: spec_1_neutral_loss_603_composition "Me Pent(2) Hex(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_603_mono_mass "602.205815"
-xref: spec_1_neutral_loss_603_avge_mass "602.537"
-xref: spec_1_neutral_loss_603_flag "false"
-xref: spec_1_neutral_loss_603_composition "Me Pent(2) Hex(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1938
-name: Hex(4)HexA(1)
-def: "Hex(4) HexA." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexa=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1938]
-xref: record_id "1938"
-xref: delta_mono_mass "824.243382"
-xref: delta_avge_mass "824.6865"
-xref: delta_composition "Hex(4) HexA"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-23 17:49:25"
-xref: date_time_modified "2017-11-23 17:49:25"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_825_mono_mass "824.243382"
-xref: spec_1_neutral_loss_825_avge_mass "824.6865"
-xref: spec_1_neutral_loss_825_flag "false"
-xref: spec_1_neutral_loss_825_composition "Hex(4) HexA"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_825_mono_mass "824.243382"
-xref: spec_1_neutral_loss_825_avge_mass "824.6865"
-xref: spec_1_neutral_loss_825_flag "false"
-xref: spec_1_neutral_loss_825_composition "Hex(4) HexA"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1939
-name: Hex(2)HexNAc(1)Pent(1)HexA(1)
-def: "Hex(2) HexNAc Pent HexA." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?pent=1&hex=2&hexa=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1939]
-xref: record_id "1939"
-xref: delta_mono_mass "835.259366"
-xref: delta_avge_mass "835.7125"
-xref: delta_composition "Pent Hex(2) HexA HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-23 17:51:41"
-xref: date_time_modified "2017-11-23 17:51:41"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_836_mono_mass "835.259366"
-xref: spec_1_neutral_loss_836_avge_mass "835.7125"
-xref: spec_1_neutral_loss_836_flag "false"
-xref: spec_1_neutral_loss_836_composition "Pent Hex(2) HexA HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_836_mono_mass "835.259366"
-xref: spec_1_neutral_loss_836_avge_mass "835.7125"
-xref: spec_1_neutral_loss_836_flag "false"
-xref: spec_1_neutral_loss_836_composition "Pent Hex(2) HexA HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1940
-name: Hex(3)HexNAc(1)HexA(1)
-def: "Hex(3) HexNAc HexA." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexa=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1940]
-xref: record_id "1940"
-xref: delta_mono_mass "865.269931"
-xref: delta_avge_mass "865.7384"
-xref: delta_composition "Hex(3) HexA HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 10:41:50"
-xref: date_time_modified "2017-11-24 10:41:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_866_mono_mass "865.269931"
-xref: spec_1_neutral_loss_866_avge_mass "865.7384"
-xref: spec_1_neutral_loss_866_flag "false"
-xref: spec_1_neutral_loss_866_composition "Hex(3) HexA HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_866_mono_mass "865.269931"
-xref: spec_1_neutral_loss_866_avge_mass "865.7384"
-xref: spec_1_neutral_loss_866_flag "false"
-xref: spec_1_neutral_loss_866_composition "Hex(3) HexA HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1941
-name: Hex(1)HexNAc(2)dHex(2)Sulf(1)
-def: "Hex HexNAc(2) dHex(2) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=2&hex=1&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1941]
-xref: record_id "1941"
-xref: delta_mono_mass "940.284201"
-xref: delta_avge_mass "940.8712"
-xref: delta_composition "O(3) S dHex(2) Hex HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 10:45:35"
-xref: date_time_modified "2017-11-24 10:45:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_941_mono_mass "940.284201"
-xref: spec_1_neutral_loss_941_avge_mass "940.8712"
-xref: spec_1_neutral_loss_941_flag "false"
-xref: spec_1_neutral_loss_941_composition "O(3) S dHex(2) Hex HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_941_mono_mass "940.284201"
-xref: spec_1_neutral_loss_941_avge_mass "940.8712"
-xref: spec_1_neutral_loss_941_flag "false"
-xref: spec_1_neutral_loss_941_composition "O(3) S dHex(2) Hex HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1942
-name: HexA(2)HexNAc(3)
-def: "HexA(2) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hexa=2&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1942]
-xref: record_id "1942"
-xref: delta_mono_mass "961.302294"
-xref: delta_avge_mass "961.8258"
-xref: delta_composition "HexA(2) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 10:48:18"
-xref: date_time_modified "2017-11-24 10:48:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_962_mono_mass "961.302294"
-xref: spec_1_neutral_loss_962_avge_mass "961.8258"
-xref: spec_1_neutral_loss_962_flag "false"
-xref: spec_1_neutral_loss_962_composition "HexA(2) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_962_mono_mass "961.302294"
-xref: spec_1_neutral_loss_962_avge_mass "961.8258"
-xref: spec_1_neutral_loss_962_flag "false"
-xref: spec_1_neutral_loss_962_composition "HexA(2) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1943
-name: dHex(1)Hex(4)HexA(1)
-def: "DHex Hex(4) HexA." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=4&hexa=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1943]
-xref: record_id "1943"
-xref: delta_mono_mass "970.301291"
-xref: delta_avge_mass "970.8277"
-xref: delta_composition "dHex Hex(4) HexA"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 10:51:51"
-xref: date_time_modified "2017-11-24 10:52:38"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_971_mono_mass "970.301291"
-xref: spec_1_neutral_loss_971_avge_mass "970.8277"
-xref: spec_1_neutral_loss_971_flag "false"
-xref: spec_1_neutral_loss_971_composition "dHex Hex(4) HexA"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_971_mono_mass "970.301291"
-xref: spec_1_neutral_loss_971_avge_mass "970.8277"
-xref: spec_1_neutral_loss_971_flag "false"
-xref: spec_1_neutral_loss_971_composition "dHex Hex(4) HexA"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1944
-name: Hex(5)HexA(1)
-def: "Hex(5) HexA." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=5&hexa=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1944]
-xref: record_id "1944"
-xref: delta_mono_mass "986.296206"
-xref: delta_avge_mass "986.8271"
-xref: delta_composition "Hex(5) HexA"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 10:54:21"
-xref: date_time_modified "2017-11-24 10:54:21"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_987_mono_mass "986.296206"
-xref: spec_1_neutral_loss_987_avge_mass "986.8271"
-xref: spec_1_neutral_loss_987_flag "false"
-xref: spec_1_neutral_loss_987_composition "Hex(5) HexA"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_987_mono_mass "986.296206"
-xref: spec_1_neutral_loss_987_avge_mass "986.8271"
-xref: spec_1_neutral_loss_987_flag "false"
-xref: spec_1_neutral_loss_987_composition "Hex(5) HexA"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1945
-name: Hex(4)HexA(1)HexNAc(1)
-def: "Hex(4) HexA HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexa=1&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1945]
-xref: record_id "1945"
-xref: delta_mono_mass "1027.322755"
-xref: delta_avge_mass "1027.879"
-xref: delta_composition "Hex(4) HexA HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 11:02:26"
-xref: date_time_modified "2017-11-24 11:03:00"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1028_mono_mass "1027.322755"
-xref: spec_1_neutral_loss_1028_avge_mass "1027.879"
-xref: spec_1_neutral_loss_1028_flag "false"
-xref: spec_1_neutral_loss_1028_composition "Hex(4) HexA HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1028_mono_mass "1027.322755"
-xref: spec_1_neutral_loss_1028_avge_mass "1027.879"
-xref: spec_1_neutral_loss_1028_flag "false"
-xref: spec_1_neutral_loss_1028_composition "Hex(4) HexA HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1946
-name: dHex(3)Hex(3)HexNAc(1)
-def: "DHex(3) Hex(3) HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=3&hex=3&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1946]
-xref: record_id "1946"
-xref: delta_mono_mass "1127.41157"
-xref: delta_avge_mass "1128.0379"
-xref: delta_composition "dHex(3) Hex(3) HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 11:05:19"
-xref: date_time_modified "2017-11-24 11:05:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1128_mono_mass "1127.41157"
-xref: spec_1_neutral_loss_1128_avge_mass "1128.0379"
-xref: spec_1_neutral_loss_1128_flag "false"
-xref: spec_1_neutral_loss_1128_composition "dHex(3) Hex(3) HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1128_mono_mass "1127.41157"
-xref: spec_1_neutral_loss_1128_avge_mass "1128.0379"
-xref: spec_1_neutral_loss_1128_flag "false"
-xref: spec_1_neutral_loss_1128_composition "dHex(3) Hex(3) HexNAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1947
-name: Hex(6)HexNAc(1)
-def: "Hex(6) HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=6&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1947]
-xref: record_id "1947"
-xref: delta_mono_mass "1175.396314"
-xref: delta_avge_mass "1176.0361"
-xref: delta_composition "Hex(6) HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 11:50:56"
-xref: date_time_modified "2018-03-28 14:15:08"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1176_mono_mass "1175.396314"
-xref: spec_1_neutral_loss_1176_avge_mass "1176.0361"
-xref: spec_1_neutral_loss_1176_flag "false"
-xref: spec_1_neutral_loss_1176_composition "Hex(6) HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1948
-name: Hex(1)HexNAc(4)dHex(1)Sulf(1)
-def: "Sulf dHex Hex HexNAc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=1&hex=1&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1948]
-xref: record_id "1948"
-xref: delta_mono_mass "1200.385037"
-xref: delta_avge_mass "1201.1151"
-xref: delta_composition "Sulf dHex Hex HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 11:56:31"
-xref: date_time_modified "2017-11-24 11:57:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1201_mono_mass "1200.385037"
-xref: spec_1_neutral_loss_1201_avge_mass "1201.1151"
-xref: spec_1_neutral_loss_1201_flag "false"
-xref: spec_1_neutral_loss_1201_composition "Sulf dHex Hex HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1201_mono_mass "1200.385037"
-xref: spec_1_neutral_loss_1201_avge_mass "1201.1151"
-xref: spec_1_neutral_loss_1201_flag "false"
-xref: spec_1_neutral_loss_1201_composition "Sulf dHex Hex HexNAc(4)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1949
-name: dHex(1)Hex(2)HexNAc(1)NeuAc(2)
-def: "DHex Hex(2) HexNAc NeuAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=2&hexnac=1&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1949]
-xref: record_id "1949"
-xref: delta_mono_mass "1255.433762"
-xref: delta_avge_mass "1256.1241"
-xref: delta_composition "dHex Hex(2) HexNAc NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 11:58:40"
-xref: date_time_modified "2017-11-24 13:36:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1256_mono_mass "1255.433762"
-xref: spec_1_neutral_loss_1256_avge_mass "1256.1241"
-xref: spec_1_neutral_loss_1256_flag "false"
-xref: spec_1_neutral_loss_1256_composition "dHex Hex(2) HexNAc NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1256_mono_mass "1255.433762"
-xref: spec_1_neutral_loss_1256_avge_mass "1256.1241"
-xref: spec_1_neutral_loss_1256_flag "false"
-xref: spec_1_neutral_loss_1256_composition "dHex Hex(2) HexNAc NeuAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1950
-name: dHex(3)Hex(3)HexNAc(2)
-def: "DHex(3) Hex(3) HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=3&hex=3&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1950]
-xref: record_id "1950"
-xref: delta_mono_mass "1330.490942"
-xref: delta_avge_mass "1331.2304"
-xref: delta_composition "dHex(3) Hex(3) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 12:05:34"
-xref: date_time_modified "2017-11-24 12:06:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1331_mono_mass "1330.490942"
-xref: spec_1_neutral_loss_1331_avge_mass "1331.2304"
-xref: spec_1_neutral_loss_1331_flag "false"
-xref: spec_1_neutral_loss_1331_composition "dHex(3) Hex(3) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1331_mono_mass "1330.490942"
-xref: spec_1_neutral_loss_1331_avge_mass "1331.2304"
-xref: spec_1_neutral_loss_1331_flag "false"
-xref: spec_1_neutral_loss_1331_composition "dHex(3) Hex(3) HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1951
-name: dHex(2)Hex(1)HexNAc(4)Sulf(1)
-def: "DHex(2) Hex HexNAc(4) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=2&hex=1&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1951]
-xref: record_id "1951"
-xref: delta_mono_mass "1346.442946"
-xref: delta_avge_mass "1347.2563"
-xref: delta_composition "Sulf dHex(2) Hex HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 12:07:49"
-xref: date_time_modified "2017-11-24 12:08:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1347_mono_mass "1346.442946"
-xref: spec_1_neutral_loss_1347_avge_mass "1347.2563"
-xref: spec_1_neutral_loss_1347_flag "false"
-xref: spec_1_neutral_loss_1347_composition "Sulf dHex(2) Hex HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1347_mono_mass "1346.442946"
-xref: spec_1_neutral_loss_1347_avge_mass "1347.2563"
-xref: spec_1_neutral_loss_1347_flag "false"
-xref: spec_1_neutral_loss_1347_composition "Sulf dHex(2) Hex HexNAc(4)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1952
-name: dHex(1)Hex(2)HexNAc(4)Sulf(2)
-def: "DHex Hex(2) HexNAc(4) Sulf(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=2&dhex=1&hex=2&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1952]
-xref: record_id "1952"
-xref: delta_mono_mass "1442.394675"
-xref: delta_avge_mass "1443.3189"
-xref: delta_composition "Sulf(2) dHex Hex(2) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 12:56:06"
-xref: date_time_modified "2017-11-24 12:57:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1443_mono_mass "1442.394675"
-xref: spec_1_neutral_loss_1443_avge_mass "1443.3189"
-xref: spec_1_neutral_loss_1443_flag "false"
-xref: spec_1_neutral_loss_1443_composition "Sulf(2) dHex Hex(2) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1443_mono_mass "1442.394675"
-xref: spec_1_neutral_loss_1443_avge_mass "1443.3189"
-xref: spec_1_neutral_loss_1443_flag "false"
-xref: spec_1_neutral_loss_1443_composition "Sulf(2) dHex Hex(2) HexNAc(4)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1953
-name: Hex(9)
-def: "Hex(9)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=9&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1953]
-xref: record_id "1953"
-xref: delta_mono_mass "1458.475412"
-xref: delta_avge_mass "1459.2654"
-xref: delta_composition "Hex(9)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 12:58:01"
-xref: date_time_modified "2017-11-24 12:58:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1459_mono_mass "1458.475412"
-xref: spec_1_neutral_loss_1459_avge_mass "1459.2654"
-xref: spec_1_neutral_loss_1459_flag "false"
-xref: spec_1_neutral_loss_1459_composition "Hex(9)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1954
-name: dHex(2)Hex(3)HexNAc(3)Sulf(1)
-def: "Sulf dHex(2) Hex(3) HexNAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=2&hex=3&hexnac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1954]
-xref: record_id "1954"
-xref: delta_mono_mass "1467.469221"
-xref: delta_avge_mass "1468.345"
-xref: delta_composition "Sulf dHex(2) Hex(3) HexNAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 12:59:19"
-xref: date_time_modified "2017-11-24 13:00:08"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1468_mono_mass "1467.469221"
-xref: spec_1_neutral_loss_1468_avge_mass "1468.345"
-xref: spec_1_neutral_loss_1468_flag "false"
-xref: spec_1_neutral_loss_1468_composition "Sulf dHex(2) Hex(3) HexNAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1468_mono_mass "1467.469221"
-xref: spec_1_neutral_loss_1468_avge_mass "1468.345"
-xref: spec_1_neutral_loss_1468_flag "false"
-xref: spec_1_neutral_loss_1468_composition "Sulf dHex(2) Hex(3) HexNAc(3)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1955
-name: dHex(2)Hex(5)HexNAc(2)Me(1)
-def: "Me dHex(2) Hex(5) HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?methyl=1&dhex=2&hex=5&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1955]
-xref: record_id "1955"
-xref: delta_mono_mass "1522.554331"
-xref: delta_avge_mass "1523.397"
-xref: delta_composition "Me dHex(2) Hex(5) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 13:02:33"
-xref: date_time_modified "2017-11-24 13:03:20"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1523_mono_mass "1522.554331"
-xref: spec_1_neutral_loss_1523_avge_mass "1523.397"
-xref: spec_1_neutral_loss_1523_flag "false"
-xref: spec_1_neutral_loss_1523_composition "Me dHex(2) Hex(5) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1523_mono_mass "1522.554331"
-xref: spec_1_neutral_loss_1523_avge_mass "1523.397"
-xref: spec_1_neutral_loss_1523_flag "false"
-xref: spec_1_neutral_loss_1523_composition "Me dHex(2) Hex(5) HexNAc(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1956
-name: dHex(2)Hex(2)HexNAc(4)Sulf(2)
-def: "Sulf(2) dHex(2) Hex(2) HexNAc(4)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=2&dhex=2&hex=2&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1956]
-xref: record_id "1956"
-xref: delta_mono_mass "1588.452584"
-xref: delta_avge_mass "1589.4601"
-xref: delta_composition "Sulf(2) dHex(2) Hex(2) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 13:04:31"
-xref: date_time_modified "2017-11-24 13:05:20"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1589_mono_mass "1588.452584"
-xref: spec_1_neutral_loss_1589_avge_mass "1589.4601"
-xref: spec_1_neutral_loss_1589_flag "false"
-xref: spec_1_neutral_loss_1589_composition "Sulf(2) dHex(2) Hex(2) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1589_mono_mass "1588.452584"
-xref: spec_1_neutral_loss_1589_avge_mass "1589.4601"
-xref: spec_1_neutral_loss_1589_flag "false"
-xref: spec_1_neutral_loss_1589_composition "Sulf(2) dHex(2) Hex(2) HexNAc(4)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1957
-name: Hex(9)HexNAc(1)
-def: "Hex(9) HexNAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=9&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1957]
-xref: record_id "1957"
-xref: delta_mono_mass "1661.554784"
-xref: delta_avge_mass "1662.4579"
-xref: delta_composition "Hex(9) HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 13:09:44"
-xref: date_time_modified "2017-11-24 13:09:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1662_mono_mass "1661.554784"
-xref: spec_1_neutral_loss_1662_avge_mass "1662.4579"
-xref: spec_1_neutral_loss_1662_flag "false"
-xref: spec_1_neutral_loss_1662_composition "Hex(9) HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1958
-name: dHex(3)Hex(2)HexNAc(4)Sulf(2)
-def: "DHex(3) Hex(2) HexNAc(4) Sulf(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=2&dhex=3&hex=2&hexnac=4&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1958]
-xref: record_id "1958"
-xref: delta_mono_mass "1734.510493"
-xref: delta_avge_mass "1735.6013"
-xref: delta_composition "Sulf(2) dHex(3) Hex(2) HexNAc(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 13:31:20"
-xref: date_time_modified "2017-11-24 13:31:20"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1735_mono_mass "1734.510493"
-xref: spec_1_neutral_loss_1735_avge_mass "1735.6013"
-xref: spec_1_neutral_loss_1735_flag "false"
-xref: spec_1_neutral_loss_1735_composition "Sulf(2) dHex(3) Hex(2) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1735_mono_mass "1734.510493"
-xref: spec_1_neutral_loss_1735_avge_mass "1735.6013"
-xref: spec_1_neutral_loss_1735_flag "false"
-xref: spec_1_neutral_loss_1735_composition "Sulf(2) dHex(3) Hex(2) HexNAc(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1959
-name: Hex(4)HexNAc(4)NeuGc(1)
-def: "Hex(4) HexNAc(4) NeuGc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=4&hexnac=4&neugc=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1959]
-xref: record_id "1959"
-xref: delta_mono_mass "1767.619116"
-xref: delta_avge_mass "1768.5865"
-xref: delta_composition "Hex(4) HexNAc(4) NeuGc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 13:33:34"
-xref: date_time_modified "2017-11-24 13:33:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1768_mono_mass "1767.619116"
-xref: spec_1_neutral_loss_1768_avge_mass "1768.5865"
-xref: spec_1_neutral_loss_1768_flag "false"
-xref: spec_1_neutral_loss_1768_composition "Hex(4) HexNAc(4) NeuGc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_1768_mono_mass "1767.619116"
-xref: spec_2_neutral_loss_1768_avge_mass "1768.5865"
-xref: spec_2_neutral_loss_1768_flag "false"
-xref: spec_2_neutral_loss_1768_composition "Hex(4) HexNAc(4) NeuGc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "O-linked glycosylation"
-xref: spec_2_neutral_loss_1768_mono_mass "1767.619116"
-xref: spec_2_neutral_loss_1768_avge_mass "1768.5865"
-xref: spec_2_neutral_loss_1768_flag "false"
-xref: spec_2_neutral_loss_1768_composition "Hex(4) HexNAc(4) NeuGc"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1960
-name: dHex(4)Hex(3)HexNAc(2)NeuAc(1)
-def: "DHex(4) Hex(3) HexNAc(2) NeuAc(1)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=4&hex=3&hexnac=2&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1960]
-xref: record_id "1960"
-xref: delta_mono_mass "1767.644268"
-xref: delta_avge_mass "1768.6262"
-xref: delta_composition "dHex(4) Hex(3) HexNAc(2) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 13:39:20"
-xref: date_time_modified "2017-11-24 13:40:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1768_mono_mass "1767.644268"
-xref: spec_1_neutral_loss_1768_avge_mass "1768.6262"
-xref: spec_1_neutral_loss_1768_flag "false"
-xref: spec_1_neutral_loss_1768_composition "dHex(4) Hex(3) HexNAc(2) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_neutral_loss_1768_mono_mass "1767.644268"
-xref: spec_1_neutral_loss_1768_avge_mass "1768.6262"
-xref: spec_1_neutral_loss_1768_flag "false"
-xref: spec_1_neutral_loss_1768_composition "dHex(4) Hex(3) HexNAc(2) NeuAc"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1961
-name: Hex(3)HexNAc(5)NeuAc(1)
-def: "Hex(3) HexNAc(5) NeuAc(1)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=5&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1961]
-xref: record_id "1961"
-xref: delta_mono_mass "1792.65075"
-xref: delta_avge_mass "1793.639"
-xref: delta_composition "Hex(3) HexNAc(5) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 13:41:14"
-xref: date_time_modified "2017-11-24 13:41:43"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1793_mono_mass "1792.65075"
-xref: spec_1_neutral_loss_1793_avge_mass "1793.639"
-xref: spec_1_neutral_loss_1793_flag "false"
-xref: spec_1_neutral_loss_1793_composition "Hex(3) HexNAc(5) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1962
-name: Hex(10)HexNAc(1)
-def: "Hex(10) HexNAc(1)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=10&hexnac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1962]
-xref: record_id "1962"
-xref: delta_mono_mass "1823.607608"
-xref: delta_avge_mass "1824.5985"
-xref: delta_composition "Hex(10) HexNAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 13:46:44"
-xref: date_time_modified "2017-11-24 13:46:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1824_mono_mass "1823.607608"
-xref: spec_1_neutral_loss_1824_avge_mass "1824.5985"
-xref: spec_1_neutral_loss_1824_flag "false"
-xref: spec_1_neutral_loss_1824_composition "Hex(10) HexNAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1963
-name: dHex(1)Hex(8)HexNAc(2)
-def: "DHex Hex(8) HexNAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=1&hex=8&hexnac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1963]
-xref: record_id "1963"
-xref: delta_mono_mass "1848.639242"
-xref: delta_avge_mass "1849.651"
-xref: delta_composition "dHex Hex(8) HexNAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 13:48:48"
-xref: date_time_modified "2017-11-24 13:48:48"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1849_mono_mass "1848.639242"
-xref: spec_1_neutral_loss_1849_avge_mass "1849.651"
-xref: spec_1_neutral_loss_1849_flag "false"
-xref: spec_1_neutral_loss_1849_composition "dHex Hex(8) HexNAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1964
-name: Hex(3)HexNAc(4)NeuAc(2)
-def: "Hex(3) HexNAc(4) NeuAc(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=4&neuac=2&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1964]
-xref: record_id "1964"
-xref: delta_mono_mass "1880.666794"
-xref: delta_avge_mass "1881.701"
-xref: delta_composition "Hex(3) HexNAc(4) NeuAc(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 13:50:19"
-xref: date_time_modified "2017-11-24 13:50:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1881_mono_mass "1880.666794"
-xref: spec_1_neutral_loss_1881_avge_mass "1881.701"
-xref: spec_1_neutral_loss_1881_flag "false"
-xref: spec_1_neutral_loss_1881_composition "Hex(3) HexNAc(4) NeuAc(2)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1965
-name: dHex(2)Hex(3)HexNAc(4)NeuAc(1)
-def: "DHex(2) Hex(3) HexNAc(4) NeuAc." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?dhex=2&hex=3&hexnac=4&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1965]
-xref: record_id "1965"
-xref: delta_mono_mass "1881.687195"
-xref: delta_avge_mass "1882.7289"
-xref: delta_composition "dHex(2) Hex(3) HexNAc(4) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 13:55:45"
-xref: date_time_modified "2017-11-24 13:56:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1882_mono_mass "1881.687195"
-xref: spec_1_neutral_loss_1882_avge_mass "1882.7289"
-xref: spec_1_neutral_loss_1882_flag "false"
-xref: spec_1_neutral_loss_1882_composition "dHex(2) Hex(3) HexNAc(4) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1966
-name: dHex(2)Hex(2)HexNAc(6)Sulf(1)
-def: "DHex(2) Hex(2) HexNAc(6) Sulf." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?sulfate=1&dhex=2&hex=2&hexnac=6&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1966]
-xref: record_id "1966"
-xref: delta_mono_mass "1914.654515"
-xref: delta_avge_mass "1915.7819"
-xref: delta_composition "Sulf dHex(2) Hex(2) HexNAc(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 14:01:17"
-xref: date_time_modified "2017-11-24 14:01:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1915_mono_mass "1914.654515"
-xref: spec_1_neutral_loss_1915_avge_mass "1915.7819"
-xref: spec_1_neutral_loss_1915_flag "false"
-xref: spec_1_neutral_loss_1915_composition "Sulf dHex(2) Hex(2) HexNAc(6)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1915_mono_mass "1914.654515"
-xref: spec_1_neutral_loss_1915_avge_mass "1915.7819"
-xref: spec_1_neutral_loss_1915_flag "false"
-xref: spec_1_neutral_loss_1915_composition "Sulf dHex(2) Hex(2) HexNAc(6)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1967
-name: Hex(5)HexNAc(4)NeuAc(1)Ac(1)
-def: "Hex(5) HexNAc(4) NeuAc Ac." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?acetyl=1&hex=5&hexnac=4&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1967]
-xref: record_id "1967"
-xref: delta_mono_mass "1955.687589"
-xref: delta_avge_mass "1956.7643"
-xref: delta_composition "Ac Hex(5) HexNAc(4) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 14:03:24"
-xref: date_time_modified "2017-11-24 14:04:26"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1956_mono_mass "1955.687589"
-xref: spec_1_neutral_loss_1956_avge_mass "1956.7643"
-xref: spec_1_neutral_loss_1956_flag "false"
-xref: spec_1_neutral_loss_1956_composition "Ac Hex(5) HexNAc(4) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1968
-name: Hex(3)HexNAc(3)NeuAc(3)
-def: "Hex(3) HexNAc(3) NeuAc(3)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=3&hexnac=3&neuac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1968]
-xref: record_id "1968"
-xref: delta_mono_mass "1968.682838"
-xref: delta_avge_mass "1969.7631"
-xref: delta_composition "Hex(3) HexNAc(3) NeuAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 14:05:50"
-xref: date_time_modified "2017-11-24 14:05:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1969_mono_mass "1968.682838"
-xref: spec_1_neutral_loss_1969_avge_mass "1969.7631"
-xref: spec_1_neutral_loss_1969_flag "false"
-xref: spec_1_neutral_loss_1969_composition "Hex(3) HexNAc(3) NeuAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_1969_mono_mass "1968.682838"
-xref: spec_1_neutral_loss_1969_avge_mass "1969.7631"
-xref: spec_1_neutral_loss_1969_flag "false"
-xref: spec_1_neutral_loss_1969_composition "Hex(3) HexNAc(3) NeuAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1969
-name: Hex(5)HexNAc(4)NeuAc(1)Ac(2)
-def: "Hex(5) HexNAc(4) NeuAc Ac(2)." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?acetyl=2&hex=5&hexnac=4&neuac=1&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1969]
-xref: record_id "1969"
-xref: delta_mono_mass "1997.698154"
-xref: delta_avge_mass "1998.801"
-xref: delta_composition "Ac(2) Hex(5) HexNAc(4) NeuAc"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-11-24 14:06:47"
-xref: date_time_modified "2017-11-24 14:06:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_1998_mono_mass "1997.698154"
-xref: spec_1_neutral_loss_1998_avge_mass "1998.801"
-xref: spec_1_neutral_loss_1998_flag "false"
-xref: spec_1_neutral_loss_1998_composition "Ac(2) Hex(5) HexNAc(4) NeuAc"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1970
-name: Unknown:162
-def: "Unidentified modification of 162.1258 found in open search." [URL:http\://www.matrixscience.com/blog/trying-to-illuminate-proteomics-dark-matter.html, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1970]
-synonym: "The elemental composition should be assumed incorrect Although it happens to be that of Diethylene glycol butyl ether, a common solvent." RELATED []
-xref: record_id "1970"
-xref: delta_mono_mass "162.125595"
-xref: delta_avge_mass "162.2267"
-xref: delta_composition "H(18) C(8) O(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-12-07 09:51:01"
-xref: date_time_modified "2018-10-17 14:27:53"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1971
-name: Unknown:177
-def: "Unidentified modification of 176.7462 found in open search." [URL:http\://www.matrixscience.com/blog/trying-to-illuminate-proteomics-dark-matter.html, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1971]
-synonym: "The elemental composition should be assumed incorrect" RELATED []
-xref: record_id "1971"
-xref: delta_mono_mass "176.744957"
-xref: delta_avge_mass "176.4788"
-xref: delta_composition "H(-7) O Fe(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-12-07 09:53:27"
-xref: date_time_modified "2017-12-07 09:53:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1972
-name: Unknown:210
-def: "Unidentified modification of 210.1616 found in open search." [URL:http\://www.matrixscience.com/blog/trying-to-illuminate-proteomics-dark-matter.html, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1972]
-synonym: "The elemental composition should be assumed incorrect" RELATED []
-xref: record_id "1972"
-xref: delta_mono_mass "210.16198"
-xref: delta_avge_mass "210.3126"
-xref: delta_composition "H(22) C(13) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-12-07 09:55:06"
-xref: date_time_modified "2017-12-07 09:55:06"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1973
-name: Unknown:216
-def: "Unidentified modification of 216.1002 found in open search." [URL:http\://www.matrixscience.com/blog/trying-to-illuminate-proteomics-dark-matter.html, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1973]
-synonym: "The elemental composition should be assumed incorrect" RELATED []
-xref: record_id "1973"
-xref: delta_mono_mass "216.099774"
-xref: delta_avge_mass "216.231"
-xref: delta_composition "H(16) C(10) O(5)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-12-07 09:59:22"
-xref: date_time_modified "2017-12-07 09:59:22"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1974
-name: Unknown:234
-def: "Unidentified modification of 234.0742 found in open search." [URL:http\://www.matrixscience.com/blog/trying-to-illuminate-proteomics-dark-matter.html, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1974]
-synonym: "The elemental composition should be assumed incorrect" RELATED []
-xref: record_id "1974"
-xref: delta_mono_mass "234.073953"
-xref: delta_avge_mass "234.2033"
-xref: delta_composition "H(14) C(9) O(7)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-12-07 10:00:16"
-xref: date_time_modified "2017-12-07 10:00:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1975
-name: Unknown:248
-def: "Unidentified modification of 248.1986 found in open search." [URL:http\://www.matrixscience.com/blog/trying-to-illuminate-proteomics-dark-matter.html, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1975]
-synonym: "The elemental composition should be assumed incorrect" RELATED []
-xref: record_id "1975"
-xref: delta_mono_mass "248.19876"
-xref: delta_avge_mass "248.359"
-xref: delta_composition "H(28) C(13) O(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-12-07 10:00:57"
-xref: date_time_modified "2017-12-07 10:00:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1976
-name: Unknown:250
-def: "Unidentified modification of 249.981 found in open search." [URL:http\://www.matrixscience.com/blog/trying-to-illuminate-proteomics-dark-matter.html, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1976]
-synonym: "The elemental composition should be assumed incorrect" RELATED []
-xref: record_id "1976"
-xref: delta_mono_mass "249.981018"
-xref: delta_avge_mass "250.2075"
-xref: delta_composition "H(4) C(10) N O(5) S"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-12-07 10:01:43"
-xref: date_time_modified "2017-12-07 10:01:43"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1977
-name: Unknown:302
-def: "Unidentified modification of 301.9864 found in open search." [URL:http\://www.matrixscience.com/blog/trying-to-illuminate-proteomics-dark-matter.html, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1977]
-synonym: "The elemental composition should be assumed incorrect" RELATED []
-xref: record_id "1977"
-xref: delta_mono_mass "301.986514"
-xref: delta_avge_mass "302.2656"
-xref: delta_composition "H(8) C(4) N(5) O(7) S(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-12-07 10:02:16"
-xref: date_time_modified "2017-12-07 10:02:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1978
-name: Unknown:306
-def: "Unidentified modification of 306.0952 found in open search." [URL:http\://www.matrixscience.com/blog/trying-to-illuminate-proteomics-dark-matter.html, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1978]
-synonym: "The elemental composition should be assumed incorrect" RELATED []
-xref: record_id "1978"
-xref: delta_mono_mass "306.095082"
-xref: delta_avge_mass "306.2659"
-xref: delta_composition "H(18) C(12) O(9)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-12-07 10:03:12"
-xref: date_time_modified "2017-12-07 10:03:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "C-term"
-xref: spec_2_position "Any C-term"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1979
-name: Unknown:420
-def: "Unidentified modification of 420.0506 found in open search." [URL:http\://www.matrixscience.com/blog/results-round-up-for-the-dark-matter-challenge.html, URL:http\://www.matrixscience.com/blog/trying-to-illuminate-proteomics-dark-matter.html, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1979]
-synonym: "Probable non-covalent adduct of CAM-DTT-DTT-CAM" RELATED []
-xref: record_id "1979"
-xref: delta_mono_mass "420.051719"
-xref: delta_avge_mass "420.5888"
-xref: delta_composition "H(24) C(12) N(2) O(6) S(4)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2017-12-07 10:03:58"
-xref: date_time_modified "2019-10-17 16:01:58"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C-term"
-xref: spec_1_position "Any C-term"
-xref: spec_1_classification "Artefact"
-xref: spec_1_neutral_loss_421_mono_mass "420.051719"
-xref: spec_1_neutral_loss_421_avge_mass "420.5888"
-xref: spec_1_neutral_loss_421_flag "false"
-xref: spec_1_neutral_loss_421_composition "H(24) C(12) N(2) O(6) S(4)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Artefact"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_421_mono_mass "420.051719"
-xref: spec_2_neutral_loss_421_avge_mass "420.5888"
-xref: spec_2_neutral_loss_421_flag "false"
-xref: spec_2_neutral_loss_421_composition "H(24) C(12) N(2) O(6) S(4)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1986
-name: Diethylphosphothione
-def: "O-diethylphosphothione." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1986]
-xref: record_id "1986"
-xref: delta_mono_mass "152.006087"
-xref: delta_avge_mass "152.1518"
-xref: delta_composition "H(9) C(4) O(2) P S"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2018-03-04 15:26:03"
-xref: date_time_modified "2018-03-08 13:03:26"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "S"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "T"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "Y"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1987
-name: Dimethylphosphothione
-def: "O-dimethylphosphothione." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1987]
-synonym: "O-ethylphosphothione" RELATED []
-xref: record_id "1987"
-xref: delta_mono_mass "123.974787"
-xref: delta_avge_mass "124.0987"
-xref: delta_composition "H(5) C(2) O(2) P S"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2018-03-04 15:31:14"
-xref: date_time_modified "2018-03-08 13:02:30"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "S"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "T"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "Y"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1989
-name: monomethylphosphothione
-def: "O-methylphosphothione." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1989]
-comment: Created by auto-catalytic dealkylation of the O-dimethylphosphothione adduct.
-xref: record_id "1989"
-xref: delta_mono_mass "109.959137"
-xref: delta_avge_mass "110.0721"
-xref: delta_composition "H(3) C O(2) P S"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2018-03-04 16:13:58"
-xref: date_time_modified "2018-03-08 13:04:11"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "S"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "T"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "Y"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1990
-name: CIGG
-def: "Ubiquitin D (FAT10) leaving after chymotrypsin digestion Cys-Ile-Gly-Gly." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1990]
-xref: record_id "1990"
-xref: delta_mono_mass "330.136176"
-xref: delta_avge_mass "330.4032"
-xref: delta_composition "H(22) C(13) N(4) O(4) S"
-xref: username_of_poster "cosmoguidry"
-xref: group_of_poster ""
-xref: date_time_posted "2018-03-13 12:00:08"
-xref: date_time_modified "2018-03-16 10:22:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1991
-name: GNLLFLACYCIGG
-def: "Ubiquitin D (FAT10) leaving after trypsin digestion Gly-Asn-Leu-Leu-Phe-Leu-Ala-Cys-Tyr-Cys-Ile-Gly-Gly." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1991]
-xref: record_id "1991"
-xref: delta_mono_mass "1324.6308"
-xref: delta_avge_mass "1325.598"
-xref: delta_composition "H(92) C(61) N(14) O(15) S(2)"
-xref: username_of_poster "cosmoguidry"
-xref: group_of_poster ""
-xref: date_time_posted "2018-03-15 15:07:14"
-xref: date_time_modified "2018-03-16 10:21:49"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1992
-name: serotonylation
-def: "5-glutamyl serotonin." [RESID:AA0528, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1992]
-xref: record_id "1992"
-xref: delta_mono_mass "159.068414"
-xref: delta_avge_mass "159.1846"
-xref: delta_composition "H(9) C(10) N O"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2018-04-17 09:27:35"
-xref: date_time_modified "2018-04-17 09:27:35"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Q"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1993
-name: TMPP-Ac:13C(9)
-def: "Heavy tris(2,4,6-trimethoxyphenyl)phosphonium acetic acid N-hydroxysuccinimide ester derivative." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1993]
-comment: The formula is reduced from H(34) to H(33) so as to give correct observed m/z values. The charge on the TMPP means that ions have one less proton than would be expected.
-xref: record_id "1993"
-xref: delta_mono_mass "581.211328"
-xref: delta_avge_mass "581.474"
-xref: delta_composition "H(33) C(20) 13C(9) O(10) P"
-xref: username_of_poster "rompais"
-xref: group_of_poster ""
-xref: date_time_posted "2018-06-26 13:54:23"
-xref: date_time_modified "2018-06-26 15:21:14"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Artefact"
-xref: spec_2_misc_notes "possible side chain reaction when labeling N-term"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Artefact"
-xref: spec_3_misc_notes "possible side chain reaction when labeling N-term"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:1999
-name: Xlink:DST[56]
-def: "DST crosslinker cleaved by sodium periodate." [URL:https\://assets.thermofisher.com/TFS-Assets/LSG/manuals/MAN0011282_DST_UG.pdf, PMID:212103, PMID:3001048, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=1999]
-xref: record_id "1999"
-xref: delta_mono_mass "55.989829"
-xref: delta_avge_mass "56.0202"
-xref: delta_composition "C(2) O(2)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2018-08-29 11:31:26"
-xref: date_time_modified "2018-08-29 11:37:13"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2001
-name: ZQG
-def: "Carbobenzoxy-L-glutaminyl-glycine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2001]
-comment: Glutamine-donor substrate for transglutaminase.
-xref: record_id "2001"
-xref: delta_mono_mass "320.100836"
-xref: delta_avge_mass "320.2973"
-xref: delta_composition "H(16) C(15) N(2) O(6)"
-xref: username_of_poster "Barbara Spolaore"
-xref: group_of_poster ""
-xref: date_time_posted "2018-09-18 12:01:47"
-xref: date_time_modified "2019-06-05 10:18:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_neutral_loss_135_mono_mass "134.036779"
-xref: spec_1_neutral_loss_135_avge_mass "134.132"
-xref: spec_1_neutral_loss_135_flag "false"
-xref: spec_1_neutral_loss_135_composition "H(6) C(8) O(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2006
-name: Haloxon
-def: "O-Dichloroethylphosphate." [PMID:4677141, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2006]
-xref: record_id "2006"
-xref: delta_mono_mass "203.950987"
-xref: delta_avge_mass "204.9763"
-xref: delta_composition "H(7) C(4) O(3) P Cl(2)"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2019-03-21 14:40:01"
-xref: date_time_modified "2019-03-21 15:45:39"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "T"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "S"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "Y"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2007
-name: Methamidophos-S
-def: "S-methyl amino phosphinate." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2007]
-xref: record_id "2007"
-xref: delta_mono_mass "108.975121"
-xref: delta_avge_mass "109.0873"
-xref: delta_composition "H(4) C N O P S"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2019-03-22 16:54:28"
-xref: date_time_modified "2019-05-22 14:56:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "S"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "T"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "Y"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2008
-name: Methamidophos-O
-def: "O-methyl amino phosphinate." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2008]
-xref: record_id "2008"
-xref: delta_mono_mass "92.997965"
-xref: delta_avge_mass "93.0217"
-xref: delta_composition "H(4) C N O(2) P"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2019-03-22 17:03:48"
-xref: date_time_modified "2019-05-22 14:57:05"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "H"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "K"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "S"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "T"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "Y"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2014
-name: Nitrene
-def: "Loss of O2; nitro photochemical decomposition." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2014]
-xref: record_id "2014"
-xref: delta_mono_mass "12.995249"
-xref: delta_avge_mass "12.9988"
-xref: delta_composition "H(-1) N"
-xref: username_of_poster "alhansen"
-xref: group_of_poster ""
-xref: date_time_posted "2019-07-10 21:24:33"
-xref: date_time_modified "2019-09-10 09:30:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2015
-name: shTMT
-def: "Super Heavy Tandem Mass Tag." [URL:https\://www.thermofisher.com/order/catalog/product/A43073, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2015]
-comment: This modification describes the Super Heavy TMT Reagent. Upon HCD, this reagent releases a reporter ion of 132.14153 (monoisotopic mass).
-synonym: "Tandem Mass Tag and TMT are registered Trademarks of Proteome Sciences plc. Super Heavy TMT" RELATED []
-xref: record_id "2015"
-xref: delta_mono_mass "235.176741"
-xref: delta_avge_mass "235.2201"
-xref: delta_composition "H(20) C(3) 13C(9) 15N(2) O(2)"
-xref: username_of_poster "rbomgard"
-xref: group_of_poster ""
-xref: date_time_posted "2019-07-10 21:42:41"
-xref: date_time_modified "2019-09-10 09:30:18"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2016
-name: TMTpro
-def: "TMTpro 16plex Tandem Mass Tag." [URL:https\://www.thermofisher.com/order/catalog/product/A44520, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2016]
-comment: This modification describes the isotope-labeled TMTpro Reagent with m/z values of the TMTpro fragment ions to be quantified for 16plex: 126.127726,127. 124761, 127.131081, 128.128116, 128.134436, 129.131471, 129.13779, 130.134825, 130.141145, 131.13818, 131.1445, 132.141535, 132.147855, 133.14489, 133.15121, and 134.148245 Additional reporter ions for 18plex: 134.154565 and 135.151600.
-synonym: "Tandem Mass Tag and TMT are registered Trademarks of Proteome Sciences plc. Also applies to TMTpro 18plex mass tags" RELATED []
-xref: record_id "2016"
-xref: delta_mono_mass "304.207146"
-xref: delta_avge_mass "304.3127"
-xref: delta_composition "H(25) C(8) 13C(7) N 15N(2) O(3)"
-xref: username_of_poster "rbomgard"
-xref: group_of_poster ""
-xref: date_time_posted "2019-09-06 19:43:32"
-xref: date_time_modified "2021-07-22 21:42:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-xref: spec_2_group "2"
-xref: spec_2_hidden "0"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Isotopic label"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Isotopic label"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "H"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Isotopic label"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "S"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Isotopic label"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "T"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2017
-name: TMTpro_zero
-def: "Native TMTpro Tandem Mass Tag." [URL:https\://www.thermofisher.com/order/catalog/product/A44518, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2017]
-comment: This modification describes the native TMTpro Reagent without isotopic label with reporter mass m/z 126.127726.
-synonym: "Tandem Mass Tag and TMT are registered Trademarks of Proteome Sciences plc." RELATED []
-xref: record_id "2017"
-xref: delta_mono_mass "295.189592"
-xref: delta_avge_mass "295.3773"
-xref: delta_composition "H(25) C(15) N(3) O(3)"
-xref: username_of_poster "rbomgard"
-xref: group_of_poster ""
-xref: date_time_posted "2019-09-06 20:04:30"
-xref: date_time_modified "2019-09-10 09:10:52"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Any N-term"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Protein N-term"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "H"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "S"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Chemical derivative"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "T"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2022
-name: Ser/Thr-KDO
-def: "Glycosylation of Serine/Threonine residues with KDO." [PMID:https://books.google.co.in/books?id=IOuPDwAAQBAJ&pg=PA333&lpg=PA333&dq=kdo+220+mass&source=bl&ots=t--BcUkzNH&sig=ACfU3U2lNj05UnTthH1BD6fS0jC6rxYpFw&hl=en&sa=X&ved=2ahUKEwjLmPfoic7nAhWA7XMBHRsiAk4Q6AEwCnoECAoQAQ#v=onepage&q=kdo%20220%20mass&f=false, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2022]
-synonym: "3-deoxy-D-manno-oct-2-ulosonic acid 2-Keto-3-Deoxy-D-Mannooctanoic Acid" RELATED []
-xref: record_id "2022"
-xref: delta_mono_mass "220.058303"
-xref: delta_avge_mass "220.1767"
-xref: delta_composition "H(12) C(8) O(7)"
-xref: username_of_poster "ramya"
-xref: group_of_poster ""
-xref: date_time_posted "2020-02-13 12:07:17"
-xref: date_time_modified "2022-10-20 12:17:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_221_mono_mass "220.058303"
-xref: spec_1_neutral_loss_221_avge_mass "220.1767"
-xref: spec_1_neutral_loss_221_flag "false"
-xref: spec_1_neutral_loss_221_composition "H(12) C(8) O(7)"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_221_mono_mass "220.058303"
-xref: spec_1_neutral_loss_221_avge_mass "220.1767"
-xref: spec_1_neutral_loss_221_flag "false"
-xref: spec_1_neutral_loss_221_composition "H(12) C(8) O(7)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2025
-name: Andro-H2O
-def: "Andrographolide with the loss of H2O." [PMID:24445406, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2025]
-xref: record_id "2025"
-xref: delta_mono_mass "332.19876"
-xref: delta_avge_mass "332.4339"
-xref: delta_composition "H(28) C(20) O(4)"
-xref: username_of_poster "nekoooooo"
-xref: group_of_poster ""
-xref: date_time_posted "2020-05-18 08:48:39"
-xref: date_time_modified "2020-05-26 15:47:33"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2027
-name: His+O(2)
-def: "Photo-induced histidine adduct." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2027]
-xref: record_id "2027"
-xref: delta_mono_mass "169.048741"
-xref: delta_avge_mass "169.1381"
-xref: delta_composition "H(7) C(6) N(3) O(3)"
-xref: username_of_poster "tomp1808"
-xref: group_of_poster ""
-xref: date_time_posted "2020-06-01 16:45:37"
-xref: date_time_modified "2020-06-09 11:01:57"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2028
-name: Hex(6)HexNAc(5)NeuAc(3)
-def: "A3G3S3." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=6&hexnac=5&neuac=3&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2028]
-xref: record_id "2028"
-xref: delta_mono_mass "2861.000054"
-xref: delta_avge_mass "2862.5699"
-xref: delta_composition "Hex(6) HexNAc(5) NeuAc(3)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2020-08-02 11:44:31"
-xref: date_time_modified "2020-08-02 11:44:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "N-linked glycosylation"
-xref: spec_1_neutral_loss_2862_mono_mass "2861.000054"
-xref: spec_1_neutral_loss_2862_avge_mass "2862.5699"
-xref: spec_1_neutral_loss_2862_flag "false"
-xref: spec_1_neutral_loss_2862_composition "Hex(6) HexNAc(5) NeuAc(3)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2029
-name: Hex(7)HexNAc(6)
-def: "A4G4." [URL:https\://glyconnect.expasy.org/browser/global/compositions/search?hex=7&hexnac=6&mode=exact, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2029]
-xref: record_id "2029"
-xref: delta_mono_mass "2352.846"
-xref: delta_avge_mass "2354.1393"
-xref: delta_composition "Hex(7) HexNAc(6)"
-xref: username_of_poster "unimod"
-xref: group_of_poster ""
-xref: date_time_posted "2020-08-02 11:47:40"
-xref: date_time_modified "2020-08-02 11:47:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_2353_mono_mass "2352.846"
-xref: spec_1_neutral_loss_2353_avge_mass "2354.1393"
-xref: spec_1_neutral_loss_2353_flag "false"
-xref: spec_1_neutral_loss_2353_composition "Hex(7) HexNAc(6)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "T"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "O-linked glycosylation"
-xref: spec_1_neutral_loss_2353_mono_mass "2352.846"
-xref: spec_1_neutral_loss_2353_avge_mass "2354.1393"
-xref: spec_1_neutral_loss_2353_flag "false"
-xref: spec_1_neutral_loss_2353_composition "Hex(7) HexNAc(6)"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "N-linked glycosylation"
-xref: spec_2_neutral_loss_2353_mono_mass "2352.846"
-xref: spec_2_neutral_loss_2353_avge_mass "2354.1393"
-xref: spec_2_neutral_loss_2353_flag "false"
-xref: spec_2_neutral_loss_2353_composition "Hex(7) HexNAc(6)"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2033
-name: Met+O(2)
-def: "Photo-induced Methionine Adduct." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2033]
-xref: record_id "2033"
-xref: delta_mono_mass "163.030314"
-xref: delta_avge_mass "163.1949"
-xref: delta_composition "H(9) C(5) N O(3) S"
-xref: username_of_poster "tomp1808"
-xref: group_of_poster ""
-xref: date_time_posted "2021-02-01 10:35:58"
-xref: date_time_modified "2021-03-09 13:26:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "Oxidative cross-link of free methionine to histidine residue in protein."
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2034
-name: Gly+O(2)
-def: "Photo-induced Glycine Adduct." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2034]
-xref: record_id "2034"
-xref: delta_mono_mass "89.011293"
-xref: delta_avge_mass "89.0501"
-xref: delta_composition "H(3) C(2) N O(3)"
-xref: username_of_poster "tomp1808"
-xref: group_of_poster ""
-xref: date_time_posted "2021-02-01 13:18:42"
-xref: date_time_modified "2021-03-09 13:27:33"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2035
-name: Pro+O(2)
-def: "Photo-induced Proline adduct." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2035]
-xref: record_id "2035"
-xref: delta_mono_mass "129.042593"
-xref: delta_avge_mass "129.114"
-xref: delta_composition "H(7) C(5) N O(3)"
-xref: username_of_poster "tomp1808"
-xref: group_of_poster ""
-xref: date_time_posted "2021-02-01 13:30:11"
-xref: date_time_modified "2021-03-09 13:28:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2036
-name: Lys+O(2)
-def: "Photo-induced Lysine adduct." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2036]
-xref: record_id "2036"
-xref: delta_mono_mass "160.084792"
-xref: delta_avge_mass "160.1711"
-xref: delta_composition "H(12) C(6) N(2) O(3)"
-xref: username_of_poster "tomp1808"
-xref: group_of_poster ""
-xref: date_time_posted "2021-02-01 13:33:53"
-xref: date_time_modified "2021-03-09 13:28:34"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2037
-name: Glu+O(2)
-def: "Photo-induced Glutamate adduct." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2037]
-xref: record_id "2037"
-xref: delta_mono_mass "161.032422"
-xref: delta_avge_mass "161.1128"
-xref: delta_composition "H(7) C(5) N O(5)"
-xref: username_of_poster "tomp1808"
-xref: group_of_poster ""
-xref: date_time_posted "2021-02-01 13:35:06"
-xref: date_time_modified "2021-03-09 13:28:59"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "H"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2039
-name: LTX+Lophotoxin
-def: "Addition of lophotoxin to tyrosine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2039]
-xref: record_id "2039"
-xref: delta_mono_mass "416.147118"
-xref: delta_avge_mass "416.4212"
-xref: delta_composition "H(24) C(22) O(8)"
-xref: username_of_poster "modchaser99"
-xref: group_of_poster ""
-xref: date_time_posted "2021-02-17 23:23:43"
-xref: date_time_modified "2021-03-09 13:32:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2040
-name: MBS+peptide
-def: "MBS_233p24 plus peptide 1250p53." [URL:https\://www.thermofisher.com/order/catalog/product/22311?us&en#/22311?us&en, PMID:https://pubmed.ncbi.nlm.nih.gov/8829804/, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2040]
-xref: record_id "2040"
-xref: delta_mono_mass "1482.77"
-xref: delta_avge_mass "1483.7597"
-xref: delta_composition "H(108) C(81) N(7) O(19)"
-xref: username_of_poster "nendicott"
-xref: group_of_poster ""
-xref: date_time_posted "2021-02-24 17:50:09"
-xref: date_time_modified "2021-03-09 13:32:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_misc_notes "Loss of MBS, peptide from KLH after trypsin digestion"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2041
-name: 3-hydroxybenzyl-phosphate
-def: "3-hydroxybenzyl phosphate." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2041]
-comment: Created by hydrolysis of the product of the reaction of 2-(o-cresyl)-4H-1,3,2-benzodioxaphosphorane-2-one with amino acids residues in proteins.
-xref: record_id "2041"
-xref: delta_mono_mass "186.008196"
-xref: delta_avge_mass "186.1018"
-xref: delta_composition "H(7) C(7) O(4) P"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2021-03-07 21:17:23"
-xref: date_time_modified "2021-03-09 13:34:53"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "Y"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2042
-name: phenyl-phosphate
-def: "Phenyl phosphate." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2042]
-comment: Created by hydrolysis of the product of the reaction of 2-(o-cresyl)-4H-1,3,2-benzodioxaphosphorane-2-one with amino acids residues in proteins.
-xref: record_id "2042"
-xref: delta_mono_mass "155.997631"
-xref: delta_avge_mass "156.0759"
-xref: delta_composition "H(5) C(6) O(3) P"
-xref: username_of_poster "lmschopfer"
-xref: group_of_poster ""
-xref: date_time_posted "2021-03-07 21:23:37"
-xref: date_time_modified "2021-03-09 13:36:06"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "S"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "T"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "Y"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2044
-name: RBS-ID_Uridine
-def: "RNA-protein UVC-crosslinked, hydrofluoride-digested uridine adduct." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2044]
-xref: record_id "2044"
-xref: delta_mono_mass "244.069536"
-xref: delta_avge_mass "244.2014"
-xref: delta_composition "H(12) C(9) N(2) O(6)"
-xref: username_of_poster "jwbaebio"
-xref: group_of_poster ""
-xref: date_time_posted "2021-06-02 01:11:04"
-xref: date_time_modified "2021-11-20 23:24:33"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "Y"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_1_misc_notes "Crosslink to all 20 amino acids. Not C-term (Missed cleavage). Partial in-source fragmentation to Uracil (loss of ribose): H(4) C(4) N(2) O(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2050
-name: shTMTpro
-def: "Super Heavy TMTpro." [URL:https\://www.thermofisher.com/order/catalog/product/A52040, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2050]
-comment: This modification describes the Super Heavy TMTpro Reagent. Upon HCD, this reagent releases a reporter ion of 135.151600 (monoisotopic mass).
-synonym: "Tandem Mass Tag and TMT are registered Trademarks of Proteome Sciences plc. TMTpro-SH 13C15 H25 15N3 O3" RELATED []
-xref: record_id "2050"
-xref: delta_mono_mass "313.231019"
-xref: delta_avge_mass "313.2473"
-xref: delta_composition "H(25) 13C(15) 15N(3) O(3)"
-xref: username_of_poster "rbomgard"
-xref: group_of_poster ""
-xref: date_time_posted "2021-07-22 21:45:43"
-xref: date_time_modified "2021-07-22 21:45:43"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2052
-name: Biotin:Aha-DADPS
-def: "Intact DADPS Biotin Alkyne tag." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2052]
-comment: Methionine is substituted in culture with azidohomoalanine. The azide group reacts with the alkyne group of DADPS Biotin Alkyne.
-xref: record_id "2052"
-xref: delta_mono_mass "922.465403"
-xref: delta_avge_mass "923.2022"
-xref: delta_composition "H(70) C(42) N(8) O(11) Si S"
-xref: username_of_poster "pluck"
-xref: group_of_poster ""
-xref: date_time_posted "2021-07-28 08:57:58"
-xref: date_time_modified "2021-07-28 09:44:43"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2053
-name: Biotin:Aha-PC
-def: "Intact PC Biotin Alkyne tag." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2053]
-comment: Methionine is substituted in culture with azidohomoalanine. The azide group reacts with the alkyne group of PC Biotin Alkyne.
-xref: record_id "2053"
-xref: delta_mono_mass "690.24316"
-xref: delta_avge_mass "690.7246"
-xref: delta_composition "H(38) C(29) N(8) O(10) S"
-xref: username_of_poster "pluck"
-xref: group_of_poster ""
-xref: date_time_posted "2021-09-30 07:29:58"
-xref: date_time_modified "2021-09-30 07:43:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "M"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2054
-name: pRBS-ID_4-thiouridine
-def: "RNA-protein UVA-crosslinked, hydrofluoride-digested 4-thiouridine adduct." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2054]
-xref: record_id "2054"
-xref: delta_mono_mass "226.058972"
-xref: delta_avge_mass "226.1861"
-xref: delta_composition "H(10) C(9) N(2) O(5)"
-xref: username_of_poster "jwbaebio"
-xref: group_of_poster ""
-xref: date_time_posted "2021-10-16 02:47:03"
-xref: date_time_modified "2022-01-10 11:09:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "F"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_1_misc_notes "Crosslink to all 20 amino acids. Not C-term (Missed cleavage). Partial in-source fragmentation & near-complete HCD-mediated fragmentation to 4-thiouracil form: H(2) C(4) N(2) O(1)"
-xref: spec_1_neutral_loss_133_mono_mass "132.042259"
-xref: spec_1_neutral_loss_133_avge_mass "132.1146"
-xref: spec_1_neutral_loss_133_flag "false"
-xref: spec_1_neutral_loss_133_composition "H(8) C(5) O(4)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2055
-name: pRBS-ID_6-thioguanosine
-def: "RNA-protein UVA-crosslinked, hydrofluoride-digested 6-thioguanosine adduct." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2055]
-xref: record_id "2055"
-xref: delta_mono_mass "265.081104"
-xref: delta_avge_mass "265.2254"
-xref: delta_composition "H(11) C(10) N(5) O(4)"
-xref: username_of_poster "jwbaebio"
-xref: group_of_poster ""
-xref: date_time_posted "2021-10-16 02:54:01"
-xref: date_time_modified "2022-01-10 11:08:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "W"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-xref: spec_1_misc_notes "Crosslink to all 20 amino acids. Not C-term (Missed cleavage). Partial in-source fragmentation & near-complete HCD-mediated fragmentation to 6-thioguanine form: H(3) C(5) N(5)"
-xref: spec_1_neutral_loss_133_mono_mass "132.042259"
-xref: spec_1_neutral_loss_133_avge_mass "132.1146"
-xref: spec_1_neutral_loss_133_flag "false"
-xref: spec_1_neutral_loss_133_composition "H(8) C(5) O(4)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2057
-name: 6C-CysPAT
-def: "Iodoacetamido-LC-Phosphonic Acid derivative." [PMID:32109415, URL:https\://www.thermofisher.com/order/catalog/product/A52285, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2057]
-synonym: "Carbamido-LC-phosphoyrlation A52285" RELATED []
-xref: record_id "2057"
-xref: delta_mono_mass "221.081695"
-xref: delta_avge_mass "221.1907"
-xref: delta_composition "H(16) C(8) N O(4) P"
-xref: username_of_poster "rbomgard"
-xref: group_of_poster ""
-xref: date_time_posted "2022-01-06 21:30:30"
-xref: date_time_modified "2022-01-07 19:11:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "0"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Artefact"
-xref: spec_3_group "3"
-xref: spec_3_hidden "0"
-xref: spec_3_site "N-term"
-xref: spec_3_position "Any N-term"
-xref: spec_3_classification "Artefact"
-xref: spec_4_group "4"
-xref: spec_4_hidden "1"
-xref: spec_4_site "H"
-xref: spec_4_position "Anywhere"
-xref: spec_4_classification "Artefact"
-xref: spec_5_group "5"
-xref: spec_5_hidden "1"
-xref: spec_5_site "D"
-xref: spec_5_position "Anywhere"
-xref: spec_5_classification "Artefact"
-xref: spec_6_group "6"
-xref: spec_6_hidden "1"
-xref: spec_6_site "E"
-xref: spec_6_position "Anywhere"
-xref: spec_6_classification "Artefact"
-xref: spec_7_group "7"
-xref: spec_7_hidden "1"
-xref: spec_7_site "S"
-xref: spec_7_position "Anywhere"
-xref: spec_7_classification "Artefact"
-xref: spec_8_group "8"
-xref: spec_8_hidden "1"
-xref: spec_8_site "T"
-xref: spec_8_position "Anywhere"
-xref: spec_8_classification "Artefact"
-xref: spec_9_group "9"
-xref: spec_9_hidden "1"
-xref: spec_9_site "Y"
-xref: spec_9_position "Anywhere"
-xref: spec_9_classification "Artefact"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2058
-name: Xlink:DSPP[210]
-def: "Intact DSPP/TBDSPP crosslinker." [PMID:31572778, URL:https\://www.thermofisher.com/order/catalog/product/A52286, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2058]
-synonym: "PhoX, tBu-PhoX (acid deprotected) A52286, A52287" RELATED []
-xref: record_id "2058"
-xref: delta_mono_mass "209.97181"
-xref: delta_avge_mass "210.0802"
-xref: delta_composition "H(3) C(8) O(5) P"
-xref: username_of_poster "rbomgard"
-xref: group_of_poster ""
-xref: date_time_posted "2022-01-06 21:47:14"
-xref: date_time_modified "2022-01-06 21:52:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2059
-name: Xlink:DSPP[228]
-def: "Water-quenched monolink of DSPP/TBDSPP crosslinker." [URL:https\://www.thermofisher.com/order/catalog/product/A52286, PMID:31572778, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2059]
-synonym: "A52286, A52287 PhoX, tBu-PhoX (acid deprotected) water quench" RELATED []
-xref: record_id "2059"
-xref: delta_mono_mass "227.982375"
-xref: delta_avge_mass "228.0955"
-xref: delta_composition "H(5) C(8) O(6) P"
-xref: username_of_poster "rbomgard"
-xref: group_of_poster ""
-xref: date_time_posted "2022-01-06 21:55:27"
-xref: date_time_modified "2022-01-06 21:57:32"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2060
-name: Xlink:DSPP[331]
-def: "Tris-quenched monolink of DSPP/TBDSPP crosslinker." [URL:https\://www.thermofisher.com/order/catalog/product/A52286, PMID:31572778, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2060]
-synonym: "C12 H14 N O8 P PhoX, tBu-PhoX (acid deprotected) Tris quench A52286, A52287" RELATED []
-xref: record_id "2060"
-xref: delta_mono_mass "331.045704"
-xref: delta_avge_mass "331.2152"
-xref: delta_composition "H(14) C(12) N O(8) P"
-xref: username_of_poster "rbomgard"
-xref: group_of_poster ""
-xref: date_time_posted "2022-01-06 22:01:09"
-xref: date_time_modified "2022-01-06 22:06:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2061
-name: Xlink:DSPP[226]
-def: "Ammonia-quenched monolink of DSPP/TBDSPP crosslinker." [URL:https\://www.thermofisher.com/order/catalog/product/A52286, PMID:31572778, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2061]
-synonym: "PhoX, tBu-PhoX (acid deprotected) ammonia quench A52286, A52287" RELATED []
-xref: record_id "2061"
-xref: delta_mono_mass "225.990534"
-xref: delta_avge_mass "226.1028"
-xref: delta_composition "H(5) C(8) N O(5) P"
-xref: username_of_poster "rbomgard"
-xref: group_of_poster ""
-xref: date_time_posted "2022-01-06 22:04:48"
-xref: date_time_modified "2022-01-07 19:13:43"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2062
-name: DBIA
-def: "Desthiobiotinylation of cysteine with DBIA probe." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2062]
-xref: record_id "2062"
-xref: delta_mono_mass "296.184841"
-xref: delta_avge_mass "296.3654"
-xref: delta_composition "H(24) C(14) N(4) O(3)"
-xref: username_of_poster "amz281"
-xref: group_of_poster ""
-xref: date_time_posted "2022-03-09 14:56:17"
-xref: date_time_modified "2022-04-18 11:09:28"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2067
-name: Mono_Ngamma-propargyl-L-Gln_desthiobiotin
-def: "Monomodification of Ngamma-propargyl-L-Gln probe with clicked desthiobiotin-azide." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2067]
-comment: - desthiobiotin-azide to enrich L-Gln-propargyl modified peptides.
-synonym: "Enrichment of modified peptides using desthiobiotin-tag on streptavidin beads" RELATED []
-xref: record_id "2067"
-xref: delta_mono_mass "596.328211"
-xref: delta_avge_mass "596.6764"
-xref: delta_composition "H(44) C(26) N(8) O(8)"
-xref: username_of_poster "KielkowskiLab"
-xref: group_of_poster ""
-xref: date_time_posted "2022-08-05 13:31:40"
-xref: date_time_modified "2024-08-12 11:07:02"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2068
-name: Di_L-Glu_Ngamma-propargyl-L-Gln_desthiobiotin
-def: "Dimodification of L-Glu and Ngamma-propargyl-L-Gln probe with clicked desthiobiotin-azide." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2068]
-comment: - desthiobiotin-azide to enrich L-Gln-propargyl modified peptides.
-xref: record_id "2068"
-xref: delta_mono_mass "709.375889"
-xref: delta_avge_mass "709.7909"
-xref: delta_composition "H(51) C(31) N(9) O(10)"
-xref: username_of_poster "KielkowskiLab"
-xref: group_of_poster ""
-xref: date_time_posted "2022-08-09 13:38:45"
-xref: date_time_modified "2024-08-12 11:06:43"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_neutral_loss_197_mono_mass "196.121178"
-xref: spec_1_neutral_loss_197_avge_mass "196.2462"
-xref: spec_1_neutral_loss_197_flag "false"
-xref: spec_1_neutral_loss_197_composition "H(16) C(10) N(2) O(2)"
-xref: spec_1_neutral_loss_728_mono_mass "727.386454"
-xref: spec_1_neutral_loss_728_avge_mass "727.8062"
-xref: spec_1_neutral_loss_728_flag "false"
-xref: spec_1_neutral_loss_728_composition "H(53) C(31) N(9) O(11)"
-xref: spec_1_neutral_loss_470_mono_mass "469.301268"
-xref: spec_1_neutral_loss_470_avge_mass "469.5783"
-xref: spec_1_neutral_loss_470_flag "false"
-xref: spec_1_neutral_loss_470_composition "H(39) C(21) N(7) O(5)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "E"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_2_neutral_loss_197_mono_mass "196.121178"
-xref: spec_2_neutral_loss_197_avge_mass "196.2462"
-xref: spec_2_neutral_loss_197_flag "false"
-xref: spec_2_neutral_loss_197_composition "H(16) C(10) N(2) O(2)"
-xref: spec_2_neutral_loss_470_mono_mass "469.301268"
-xref: spec_2_neutral_loss_470_avge_mass "469.5783"
-xref: spec_2_neutral_loss_470_flag "false"
-xref: spec_2_neutral_loss_470_composition "H(39) C(21) N(7) O(5)"
-xref: spec_2_neutral_loss_728_mono_mass "727.386454"
-xref: spec_2_neutral_loss_728_avge_mass "727.8062"
-xref: spec_2_neutral_loss_728_flag "false"
-xref: spec_2_neutral_loss_728_composition "H(53) C(31) N(9) O(11)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2069
-name: Di_L-Gln_Ngamma-propargyl-L-Gln_desthiobiotin
-def: "Dimodification of L-Gln and Ngamma-propargyl-L-Gln probe with clicked desthiobiotin-azide." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2069]
-comment: - desthiobiotin-azide to enrich L-Gln-propargyl modified peptides.
-xref: record_id "2069"
-xref: delta_mono_mass "708.391873"
-xref: delta_avge_mass "708.8062"
-xref: delta_composition "H(52) C(31) N(10) O(9)"
-xref: username_of_poster "KielkowskiLab"
-xref: group_of_poster ""
-xref: date_time_posted "2022-08-09 13:45:33"
-xref: date_time_modified "2024-08-12 11:06:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "D"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_neutral_loss_197_mono_mass "196.121178"
-xref: spec_1_neutral_loss_197_avge_mass "196.2462"
-xref: spec_1_neutral_loss_197_flag "false"
-xref: spec_1_neutral_loss_197_composition "H(16) C(10) N(2) O(2)"
-xref: spec_1_neutral_loss_727_mono_mass "726.402438"
-xref: spec_1_neutral_loss_727_avge_mass "726.8215"
-xref: spec_1_neutral_loss_727_flag "false"
-xref: spec_1_neutral_loss_727_composition "H(54) C(31) N(10) O(10)"
-xref: spec_1_neutral_loss_470_mono_mass "469.301268"
-xref: spec_1_neutral_loss_470_avge_mass "469.5783"
-xref: spec_1_neutral_loss_470_flag "false"
-xref: spec_1_neutral_loss_470_composition "H(39) C(21) N(7) O(5)"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "E"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_2_neutral_loss_727_mono_mass "726.402438"
-xref: spec_2_neutral_loss_727_avge_mass "726.8215"
-xref: spec_2_neutral_loss_727_flag "false"
-xref: spec_2_neutral_loss_727_composition "H(54) C(31) N(10) O(10)"
-xref: spec_2_neutral_loss_470_mono_mass "469.301268"
-xref: spec_2_neutral_loss_470_avge_mass "469.5783"
-xref: spec_2_neutral_loss_470_flag "false"
-xref: spec_2_neutral_loss_470_composition "H(39) C(21) N(7) O(5)"
-xref: spec_2_neutral_loss_197_mono_mass "196.121178"
-xref: spec_2_neutral_loss_197_avge_mass "196.2462"
-xref: spec_2_neutral_loss_197_flag "false"
-xref: spec_2_neutral_loss_197_composition "H(16) C(10) N(2) O(2)"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2070
-name: L-Gln
-def: "Monomodification with glutamine." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2070]
-xref: record_id "2070"
-xref: delta_mono_mass "128.058578"
-xref: delta_avge_mass "128.1292"
-xref: delta_composition "H(8) C(5) N(2) O(2)"
-xref: username_of_poster "KielkowskiLab"
-xref: group_of_poster ""
-xref: date_time_posted "2022-08-25 13:15:56"
-xref: date_time_modified "2022-10-20 14:06:31"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "E"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "D"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2072
-name: Glyceroyl
-def: "Glyceroylation." [PMID:35046029, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2072]
-xref: record_id "2072"
-xref: delta_mono_mass "88.016044"
-xref: delta_avge_mass "88.0621"
-xref: delta_composition "H(4) C(3) O(3)"
-xref: username_of_poster "heremans"
-xref: group_of_poster ""
-xref: date_time_posted "2022-09-06 09:03:01"
-xref: date_time_modified "2022-10-20 14:05:50"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "N-term"
-xref: spec_2_position "Protein N-term"
-xref: spec_2_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2073
-name: N6pAMP
-def: "Plain N6-Propargyl-AMP modified proteins without any clicked enrichment tag." [PMID:21942216, PMID:31980631, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2073]
-xref: record_id "2073"
-xref: delta_mono_mass "367.06817"
-xref: delta_avge_mass "367.2539"
-xref: delta_composition "H(14) C(13) N(5) O(6) P"
-xref: username_of_poster "KielkowskiLab"
-xref: group_of_poster ""
-xref: date_time_posted "2023-02-06 14:36:27"
-xref: date_time_modified "2023-10-05 14:38:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "S"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "T"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "Y"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2074
-name: DABCYL-C2-maleimide
-def: "DABCYL-C2-maleimide Thiol-reactive dye for fluorescence labelling of proteins." [PMID:25197743, URL:https\://www.aatbio.com/products/dabcyl-c2-maleimide, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2074]
-xref: record_id "2074"
-xref: delta_mono_mass "391.16444"
-xref: delta_avge_mass "391.4231"
-xref: delta_composition "H(21) C(21) N(5) O(3)"
-xref: username_of_poster "amedalin"
-xref: group_of_poster ""
-xref: date_time_posted "2023-02-15 13:46:57"
-xref: date_time_modified "2023-10-05 14:38:24"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_1_neutral_loss_252_mono_mass "251.105862"
-xref: spec_1_neutral_loss_252_avge_mass "251.2832"
-xref: spec_1_neutral_loss_252_flag "false"
-xref: spec_1_neutral_loss_252_composition "H(13) C(15) N(3) O"
-xref: spec_1_neutral_loss_0_mono_mass "0"
-xref: spec_1_neutral_loss_0_avge_mass "0"
-xref: spec_1_neutral_loss_0_flag "false"
-xref: spec_1_neutral_loss_0_composition "0"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_2_neutral_loss_0_mono_mass "0"
-xref: spec_2_neutral_loss_0_avge_mass "0"
-xref: spec_2_neutral_loss_0_flag "false"
-xref: spec_2_neutral_loss_0_composition "0"
-xref: spec_2_neutral_loss_252_mono_mass "251.105862"
-xref: spec_2_neutral_loss_252_avge_mass "251.2832"
-xref: spec_2_neutral_loss_252_flag "false"
-xref: spec_2_neutral_loss_252_composition "H(13) C(15) N(3) O"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2079
-name: NBF
-def: "Thiol blocking reagent." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2079]
-synonym: "4-Chloro-7-nitrobenzofurazan NBD Chloride" RELATED []
-xref: record_id "2079"
-xref: delta_mono_mass "163.001791"
-xref: delta_avge_mass "163.0904"
-xref: delta_composition "H C(6) N(3) O(3)"
-xref: username_of_poster "thibautvignane"
-xref: group_of_poster ""
-xref: date_time_posted "2023-03-30 16:05:51"
-xref: date_time_modified "2024-08-12 10:35:44"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-xref: spec_2_group "2"
-xref: spec_2_hidden "1"
-xref: spec_2_site "K"
-xref: spec_2_position "Anywhere"
-xref: spec_2_classification "Chemical derivative"
-xref: spec_3_group "3"
-xref: spec_3_hidden "1"
-xref: spec_3_site "R"
-xref: spec_3_position "Anywhere"
-xref: spec_3_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2080
-name: DCP
-def: "Dimedone-Based Chemical Probes." [PMID:20513473, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2080]
-synonym: "Cleaved Cysteine Sulfenic Acid Probe (DCP-Bio1) Use for enrichment of cysteine oxidation" RELATED []
-xref: record_id "2080"
-xref: delta_mono_mass "168.078644"
-xref: delta_avge_mass "168.1898"
-xref: delta_composition "H(12) C(9) O(3)"
-xref: username_of_poster "thibautvignane"
-xref: group_of_poster ""
-xref: date_time_posted "2023-04-19 18:49:30"
-xref: date_time_modified "2024-08-12 10:35:12"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2081
-name: Ethynyl
-def: "Ethynlation of cysteine residues." [PMID:32233093, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2081]
-xref: record_id "2081"
-xref: delta_mono_mass "24"
-xref: delta_avge_mass "24.0214"
-xref: delta_composition "C(2)"
-xref: username_of_poster "bdwyer"
-xref: group_of_poster ""
-xref: date_time_posted "2023-07-29 02:40:17"
-xref: date_time_modified "2023-10-05 14:37:06"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2082
-name: QQTGG
-def: "SUMOylation leaving QQTGG." [PMID:28112733, PMID:28112733, PMID:25218447, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2082]
-xref: record_id "2082"
-xref: delta_mono_mass "471.207761"
-xref: delta_avge_mass "471.465"
-xref: delta_composition "H(29) C(18) N(7) O(8)"
-xref: username_of_poster "jonesar"
-xref: group_of_poster ""
-xref: date_time_posted "2023-09-27 09:55:30"
-xref: date_time_modified "2023-10-05 14:36:46"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2083
-name: Pyro-QQTGG
-def: "SUMOylation leaving Pyro-QQTGG." [PMID:25218447, PMID:28112733, PMID:28112733, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2083]
-xref: record_id "2083"
-xref: delta_mono_mass "454.181212"
-xref: delta_avge_mass "454.4344"
-xref: delta_composition "H(26) C(18) N(6) O(8)"
-xref: username_of_poster "jonesar"
-xref: group_of_poster ""
-xref: date_time_posted "2023-09-27 09:57:43"
-xref: date_time_modified "2023-10-05 14:36:23"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2084
-name: NQTGG
-def: "SUMOylation leaving NQTGG." [PMID:32047143, PMID:29048423, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2084]
-xref: record_id "2084"
-xref: delta_mono_mass "457.192111"
-xref: delta_avge_mass "457.4384"
-xref: delta_composition "H(27) C(17) N(7) O(8)"
-xref: username_of_poster "jonesar"
-xref: group_of_poster ""
-xref: date_time_posted "2023-09-27 10:05:13"
-xref: date_time_modified "2023-10-05 14:36:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2085
-name: DVFQQQTGG
-def: "SUMOylation by Endogenous SUMO2/3 following Lys C and Asp-N serial digestion." [PMID:29942033, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2085]
-xref: record_id "2085"
-xref: delta_mono_mass "960.43011"
-xref: delta_avge_mass "960.9865"
-xref: delta_composition "H(60) C(41) N(12) O(15)"
-xref: username_of_poster "jonesar"
-xref: group_of_poster ""
-xref: date_time_posted "2023-09-27 10:06:06"
-xref: date_time_modified "2023-10-05 14:35:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2086
-name: iST-NHS specific cysteine modification
-def: "Preomics iST-NHS Kit specific cysteine modification." [URL:https\://www.preomics.com/products/ist-nhs, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2086]
-comment: The lysis buffer in the iST-NHS kit, called LYSE-NHS, does not contain primary amines and therefore does not interfere with chemical labeling. The LYSE-NHS contains a distinct alkylation agent. Please consider the following as fixed modification in your database search: Specific cysteine modification (C6H11NO), specificity [C], mass shift +113.084 Da.
-xref: record_id "2086"
-xref: delta_mono_mass "113.084064"
-xref: delta_avge_mass "113.1576"
-xref: delta_composition "H(11) C(6) N O"
-xref: username_of_poster "dzolg"
-xref: group_of_poster ""
-xref: date_time_posted "2023-12-04 11:10:14"
-xref: date_time_modified "2024-07-08 16:54:51"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2088
-name: Label:13C(2)15N(1)
-def: "13C(2) 15N(1) Silac label." [URL:https\://isotope.com/de-de/microbiological-and-pyrogen-tested-mpt/glycine-13c5-15n-cnlm-1673-h-mpt, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2088]
-xref: record_id "2088"
-xref: delta_mono_mass "3.003745"
-xref: delta_avge_mass "2.9787"
-xref: delta_composition "C(-2) 13C(2) N(-1) 15N"
-xref: username_of_poster "jonasfoerster"
-xref: group_of_poster ""
-xref: date_time_posted "2024-01-08 10:29:39"
-xref: date_time_modified "2024-02-29 10:49:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "G"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Isotopic label"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2106
-name: DPIA
-def: "Desthiobiotinylation of cysteine with DPIA (Desthiobiotin polyethyleneoxide iodoacetamide) probe." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2106]
-xref: record_id "2106"
-xref: delta_mono_mass "455.274384"
-xref: delta_avge_mass "455.5484"
-xref: delta_composition "H(37) C(21) N(5) O(6)"
-xref: username_of_poster "bdwyer"
-xref: group_of_poster ""
-xref: date_time_posted "2024-04-22 22:51:46"
-xref: date_time_modified "2024-04-22 22:51:46"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Chemical derivative"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2107
-name: Acetoacetyl
-def: "Acetoacetylation." [URL:https\://www.genome.jp/entry/C00332, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2107]
-xref: record_id "2107"
-xref: delta_mono_mass "84.021129"
-xref: delta_avge_mass "84.0734"
-xref: delta_composition "H(4) C(4) O(2)"
-xref: username_of_poster "JakobB"
-xref: group_of_poster ""
-xref: date_time_posted "2024-06-22 12:17:22"
-xref: date_time_modified "2024-07-05 12:18:20"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2108
-name: Isovaleryl
-def: "Isovalerylation." [URL:https\://www.genome.jp/entry/C02939, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2108]
-xref: record_id "2108"
-xref: delta_mono_mass "84.057515"
-xref: delta_avge_mass "84.1164"
-xref: delta_composition "H(8) C(5) O"
-xref: username_of_poster "JakobB"
-xref: group_of_poster ""
-xref: date_time_posted "2024-06-22 12:24:23"
-xref: date_time_modified "2024-06-28 10:55:54"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2109
-name: 2-methylbutyryl
-def: "2-methylbutyrylation." [URL:https\://www.kegg.jp/entry/C01033, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2109]
-xref: record_id "2109"
-xref: delta_mono_mass "84.057515"
-xref: delta_avge_mass "84.1164"
-xref: delta_composition "H(8) C(5) O"
-xref: username_of_poster "JakobB"
-xref: group_of_poster ""
-xref: date_time_posted "2024-06-22 12:30:37"
-xref: date_time_modified "2024-06-28 10:57:45"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2110
-name: Tiglyl
-def: "Tiglylation." [URL:https\://www.genome.jp/entry/C03345, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2110]
-xref: record_id "2110"
-xref: delta_mono_mass "82.041865"
-xref: delta_avge_mass "82.1005"
-xref: delta_composition "H(6) C(5) O"
-xref: username_of_poster "JakobB"
-xref: group_of_poster ""
-xref: date_time_posted "2024-06-22 12:33:24"
-xref: date_time_modified "2024-07-05 12:15:40"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2111
-name: 3-methylglutaryl
-def: "3-methylglutarylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2111]
-xref: record_id "2111"
-xref: delta_mono_mass "128.047344"
-xref: delta_avge_mass "128.1259"
-xref: delta_composition "H(8) C(6) O(3)"
-xref: username_of_poster "JakobB"
-xref: group_of_poster ""
-xref: date_time_posted "2024-06-22 14:19:16"
-xref: date_time_modified "2024-06-22 14:19:16"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2112
-name: 3-methylglutaconyl
-def: "3-methylglutaconylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2112]
-xref: record_id "2112"
-xref: delta_mono_mass "126.031694"
-xref: delta_avge_mass "126.11"
-xref: delta_composition "H(6) C(6) O(3)"
-xref: username_of_poster "JakobB"
-xref: group_of_poster ""
-xref: date_time_posted "2024-06-22 14:21:47"
-xref: date_time_modified "2024-06-22 14:21:47"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2113
-name: 3-hydroxy-3-methylglutaryl
-def: "3-hydroxy-3-methylglutarylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2113]
-xref: record_id "2113"
-xref: delta_mono_mass "144.042259"
-xref: delta_avge_mass "144.1253"
-xref: delta_composition "H(8) C(6) O(4)"
-xref: username_of_poster "JakobB"
-xref: group_of_poster ""
-xref: date_time_posted "2024-06-22 14:24:06"
-xref: date_time_modified "2024-06-22 14:24:06"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2114
-name: Lactylation
-def: "Lactylation(Lac)." [PMID:31645732, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2114]
-xref: record_id "2114"
-xref: delta_mono_mass "72.021129"
-xref: delta_avge_mass "72.0627"
-xref: delta_composition "H(4) C(3) O(2)"
-xref: username_of_poster "cpu1107"
-xref: group_of_poster ""
-xref: date_time_posted "2024-06-24 10:56:15"
-xref: date_time_modified "2024-08-09 09:54:27"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2115
-name: Pyruvoyl
-def: "Pyruvoylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2115]
-xref: record_id "2115"
-xref: delta_mono_mass "70.005479"
-xref: delta_avge_mass "70.0468"
-xref: delta_composition "H(2) C(3) O(2)"
-xref: username_of_poster "JakobB"
-xref: group_of_poster ""
-xref: date_time_posted "2024-06-24 18:33:34"
-xref: date_time_modified "2024-08-09 09:54:42"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2116
-name: Glyoxylyl
-def: "Glyoxylylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2116]
-xref: record_id "2116"
-xref: delta_mono_mass "55.989829"
-xref: delta_avge_mass "56.0202"
-xref: delta_composition "C(2) O(2)"
-xref: username_of_poster "JakobB"
-xref: group_of_poster ""
-xref: date_time_posted "2024-06-24 19:20:20"
-xref: date_time_modified "2024-08-09 09:54:55"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2117
-name: Itaconatyl
-def: "Itaconatylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2117]
-xref: record_id "2117"
-xref: delta_mono_mass "130.026609"
-xref: delta_avge_mass "130.0987"
-xref: delta_composition "H(6) C(5) O(4)"
-xref: username_of_poster "JakobB"
-xref: group_of_poster ""
-xref: date_time_posted "2024-06-24 20:02:30"
-xref: date_time_modified "2024-08-09 09:55:04"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "C"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2118
-name: Itaconyl
-def: "Itaconylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2118]
-xref: record_id "2118"
-xref: delta_mono_mass "112.016044"
-xref: delta_avge_mass "112.0835"
-xref: delta_composition "H(4) C(5) O(3)"
-xref: username_of_poster "JakobB"
-xref: group_of_poster ""
-xref: date_time_posted "2024-06-26 14:01:07"
-xref: date_time_modified "2024-08-09 09:55:19"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2119
-name: ValGly
-def: "UFMylation residue." [PMID:8383789, PMID:33066455, PMID:http://www.ncbi.nlm.nih.gov/pubmed/35756382, PMID:35756382, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2119]
-comment: The valine glycine residues left on ufmylated lysine after tryptic digestion.
-synonym: "UFMylation leaving VG tag valineglycine" RELATED []
-xref: record_id "2119"
-xref: delta_mono_mass "156.089878"
-xref: delta_avge_mass "156.1824"
-xref: delta_composition "H(12) C(7) N(2) O(2)"
-xref: username_of_poster "pscaturro"
-xref: group_of_poster ""
-xref: date_time_posted "2024-06-26 14:09:36"
-xref: date_time_modified "2024-06-26 14:09:36"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2120
-name: Pentanoyl
-def: "Pentanoylation." [URL:https\://www.genome.jp/entry/C00888, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2120]
-synonym: "Valeryl" RELATED []
-xref: record_id "2120"
-xref: delta_mono_mass "84.057515"
-xref: delta_avge_mass "84.1164"
-xref: delta_composition "H(8) C(5) O"
-xref: username_of_poster "JakobB"
-xref: group_of_poster ""
-xref: date_time_posted "2024-06-26 14:12:23"
-xref: date_time_modified "2024-06-28 10:53:01"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2121
-name: Hexanoyl
-def: "Hexanoylation." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2121]
-xref: record_id "2121"
-xref: delta_mono_mass "98.073165"
-xref: delta_avge_mass "98.143"
-xref: delta_composition "H(10) C(6) O"
-xref: username_of_poster "JakobB"
-xref: group_of_poster ""
-xref: date_time_posted "2024-06-26 14:24:17"
-xref: date_time_modified "2024-06-26 14:24:17"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Post-translational"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2122
-name: Label:13C(6)15N(2)+TMT6plex
-def: "Sixplex Tandem Mass Tag 13C(6) 15N(2) Silac label." [PMID:34847359, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2122]
-comment: Tandem Mass Tag and TMT are registered Trademarks of Proteome Sciences plc.
-xref: record_id "2122"
-xref: delta_mono_mass "237.177131"
-xref: delta_avge_mass "237.2062"
-xref: delta_composition "H(20) C(2) 13C(10) N(-1) 15N(3) O(2)"
-xref: username_of_poster "dzolg"
-xref: group_of_poster ""
-xref: date_time_posted "2024-07-01 12:49:15"
-xref: date_time_modified "2024-08-12 11:33:03"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Multiple"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2123
-name: Label:13C(6)15N(2)+TMTpro
-def: "TMTpro Tandem Mass Tag 13C(6) 15N(2) Silac label." [PMID:34847359, UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2123]
-comment: Tandem Mass Tag and TMT are registered Trademarks of Proteome Sciences plc.
-xref: record_id "2123"
-xref: delta_mono_mass "312.221344"
-xref: delta_avge_mass "312.2554"
-xref: delta_composition "H(25) C(2) 13C(13) N(-1) 15N(4) O(3)"
-xref: username_of_poster "dzolg"
-xref: group_of_poster ""
-xref: date_time_posted "2024-07-01 12:51:56"
-xref: date_time_modified "2024-08-12 11:33:20"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "K"
-xref: spec_1_position "Anywhere"
-xref: spec_1_classification "Multiple"
-is_a: UNIMOD:0 ! unimod root node
-
-
-[Term]
-id: UNIMOD:2126
-name: 2PCA-triazole-ethanethiol
-def: "Cleaved 2PCA clicked to biotin-SS-azide." [UNIMODURL:http\://www.unimod.org/modifications_view.php?editid1=2126]
-xref: record_id "2126"
-xref: delta_mono_mass "216.046967"
-xref: delta_avge_mass "216.2623"
-xref: delta_composition "H(8) C(10) N(4) S"
-xref: username_of_poster "pscaturro"
-xref: group_of_poster ""
-xref: date_time_posted "2024-07-08 10:09:29"
-xref: date_time_modified "2024-08-09 09:56:09"
-xref: approved "0"
-xref: spec_1_group "1"
-xref: spec_1_hidden "1"
-xref: spec_1_site "N-term"
-xref: spec_1_position "Any N-term"
-xref: spec_1_classification "Other"
-is_a: UNIMOD:0 ! unimod root node
-
-
diff --git a/rustyms-generate-databases/src/gnome.rs b/rustyms-generate-databases/src/gnome.rs
index 953a7521..6c114088 100644
--- a/rustyms-generate-databases/src/gnome.rs
+++ b/rustyms-generate-databases/src/gnome.rs
@@ -70,7 +70,7 @@ fn find_mass(mods: &HashMap<String, GNOmeModification>, mut name: String) -> Opt
     mass
 }
 
-#[allow(dead_code)]
+#[expect(dead_code)]
 mod gnome_terms {
     pub const SUBSUMPTION_MOLECULAR_WEIGHT: &str = "GNO:00000012";
     pub const SUBSUMPTION_BASECOMPOSITION: &str = "GNO:00000013";
diff --git a/rustyms-generate-imgt/Cargo.toml b/rustyms-generate-imgt/Cargo.toml
index 9327908b..a89edacc 100644
--- a/rustyms-generate-imgt/Cargo.toml
+++ b/rustyms-generate-imgt/Cargo.toml
@@ -17,3 +17,6 @@ similar = { workspace = true }
 
 [features]
 rayon = []
+
+[lints]
+workspace = true
diff --git a/rustyms-generate-imgt/src/combine.rs b/rustyms-generate-imgt/src/combine.rs
index a6490afa..79825621 100644
--- a/rustyms-generate-imgt/src/combine.rs
+++ b/rustyms-generate-imgt/src/combine.rs
@@ -3,8 +3,8 @@ use std::fmt::Write;
 
 use itertools::Itertools;
 use rustyms::align::AlignScoring;
-use rustyms::peptide::{Annotation, Region};
-use rustyms::LinearPeptide;
+use rustyms::peptidoform::{Annotation, Region};
+use rustyms::Peptidoform;
 use rustyms::UnAmbiguous;
 
 use crate::imgt_gene::IMGTGene;
@@ -294,7 +294,7 @@ impl std::fmt::Display for TemporaryGermline {
 #[derive(Debug, PartialEq, Eq)]
 struct TemporarySequence {
     acc: Vec<String>,
-    sequence: LinearPeptide<UnAmbiguous>,
+    sequence: Peptidoform<UnAmbiguous>,
     regions: HashMap<Vec<(Region, usize)>, Vec<usize>>,
     annotations: HashMap<Vec<(Annotation, usize)>, Vec<usize>>,
     dna: HashMap<String, Vec<usize>>,
diff --git a/rustyms-generate-imgt/src/imgt_gene.rs b/rustyms-generate-imgt/src/imgt_gene.rs
index 30709eea..74228eed 100644
--- a/rustyms-generate-imgt/src/imgt_gene.rs
+++ b/rustyms-generate-imgt/src/imgt_gene.rs
@@ -3,7 +3,7 @@ use std::fmt::Display;
 
 use itertools::Itertools;
 use rustyms::{
-    peptide::{Annotation, Region},
+    peptidoform::{Annotation, Region},
     AminoAcid, CheckedAminoAcid,
 };
 
diff --git a/rustyms-generate-imgt/src/main.rs b/rustyms-generate-imgt/src/main.rs
index f9113000..c7d58329 100644
--- a/rustyms-generate-imgt/src/main.rs
+++ b/rustyms-generate-imgt/src/main.rs
@@ -18,7 +18,7 @@ use crate::shared::*;
 
 use itertools::Itertools;
 use rustyms::{
-    peptide::{Annotation, Region},
+    peptidoform::{Annotation, Region},
     *,
 };
 use structs::{Location, SequenceRegion};
diff --git a/rustyms-generate-imgt/src/structs.rs b/rustyms-generate-imgt/src/structs.rs
index 77050c1f..3f1bb907 100644
--- a/rustyms-generate-imgt/src/structs.rs
+++ b/rustyms-generate-imgt/src/structs.rs
@@ -63,7 +63,10 @@ impl Display for Region {
     }
 }
 
-pub type SequenceRegion = (rustyms::peptide::Region, (Vec<AminoAcid>, Location, String));
+pub type SequenceRegion = (
+    rustyms::peptidoform::Region,
+    (Vec<AminoAcid>, Location, String),
+);
 
 #[derive(Clone, Debug, Hash, Eq, PartialEq)]
 pub enum Location {
diff --git a/rustyms-imgt-generate/data/imgt_small.dat b/rustyms-imgt-generate/data/imgt_small.dat
deleted file mode 100644
index 6440c197..00000000
--- a/rustyms-imgt-generate/data/imgt_small.dat
+++ /dev/null
@@ -1,2127 +0,0 @@
-//
-ID   AF052386; SV 1; linear; cDNA; STD; HUM; 440 BP.
-XX
-AC   AF052386;
-XX
-DT   27-JAN-1999 (Rel. 199904-3, arrived in LIGM-DB)
-DT   15-JUN-2024 (Rel. 202424-6, Last updated, Version 8)
-XX
-DE   Homo sapiens lymphoma 7 IgA heavy chain variable region mRNA, partial cds.
-XX
-KW   antigen receptor; Immunoglobulin superfamily (IgSF); immunoglobulin (IG);
-KW   IG-Heavy; IG-Heavy-Alpha; constant; variable; diversity; joining; regular;
-KW   cDNA; undefined; rearranged; productive; L-V-D-J-C-sequence.
-XX
-OS   Homo sapiens (human)
-OC   cellular organisms; Eukaryota; Opisthokonta; Metazoa; Eumetazoa; Bilateria;
-OC   Deuterostomia; Chordata; Craniata; Vertebrata; Gnathostomata; Teleostomi;
-OC   Euteleostomi; Sarcopterygii; Dipnotetrapodomorpha; Tetrapoda; Amniota;
-OC   Mammalia; Theria; Eutheria; Boreoeutheria; Euarchontoglires; Primates;
-OC   Haplorrhini; Simiiformes; Catarrhini; Hominoidea; Hominidae; Homininae;
-OC   Homo; Homo sapiens.
-XX
-RN   [1]
-RP   1-440
-RA   Shinohara S., Satorius C.;
-RT   ;
-RL   Submitted (14-FEB-2005) to the INSDC.
-RL   Contact:Satoshi Shinohara National Institute of Arthritis and
-RL   Musculoskeletal and Skin Diseases, Autoimmunity Branch; 9000 Rockville Pike
-RL   Bldg10/6D44, Bethesda, Maryland 20892-1592, USA
-XX
-RN   [2]
-RP   1-440
-RA   Aarts W.M.;
-RT   ;
-RL   Submitted (06-MAR-1998) to the INSDC.
-RL   Pathology, Academic Medical Center, Meibergdreef 9, Amsterdam 1105 AZ, the
-RL   Netherlands
-XX
-DR   MD5; 6270654450eacc9dffd4a9bdd8f93468.
-XX
-CC   IMGT/LIGM-DB annotation level: automatic
-XX
-FH   Key                 Location/Qualifiers
-FH
-FT   L-V-D-J-C-SEQUENCE  <1..>440
-FT                       /partial
-FT                       /cell_type="B-cell"
-FT                       /chromosome="14"
-FT                       /map="14q32.33"
-FT                       /organism="Homo sapiens"
-FT                       /productive
-FT                       /tissue_type="primary cutaneous lymphoma 7 alpha       
-FT                                (immunocytoma)"
-FT   L-V-D-J-C-REGION    1..>440
-FT                       /partial
-FT                       /translation="MDWTWRILFLVAAATGAHSHVQLVQSGPEVKKPGASVRVSC
-FT                       KTSGYTFIDYFIHWVRQAPGQGLEWLGWINPYSGDTNCAQTFQGRVSMTRDRSLT
-FT                       TAFMKMPRLRSDDTALYFCARGLQDFTLDSWGQGTLVVVSSASPTSPKVF"
-FT                       /db_xref="PID:g3540273"
-FT                       /product="IgA heavy chain variable region"
-FT   L-V-D-J-REGION      1..411
-FT                       /translation="MDWTWRILFLVAAATGAHSHVQLVQSGPEVKKPGASVRVSC
-FT                       KTSGYTFIDYFIHWVRQAPGQGLEWLGWINPYSGDTNCAQTFQGRVSMTRDRSLT
-FT                       TAFMKMPRLRSDDTALYFCARGLQDFTLDSWGQGTLVVVSS"
-FT   L-V-D-REGION        1..363
-FT                       /translation="MDWTWRILFLVAAATGAHSHVQLVQSGPEVKKPGASVRVSC
-FT                       KTSGYTFIDYFIHWVRQAPGQGLEWLGWINPYSGDTNCAQTFQGRVSMTRDRSLT
-FT                       TAFMKMPRLRSDDTALYFCARGLQD"
-FT   L-V-REGION          1..350
-FT                       /translation="MDWTWRILFLVAAATGAHSHVQLVQSGPEVKKPGASVRVSC
-FT                       KTSGYTFIDYFIHWVRQAPGQGLEWLGWINPYSGDTNCAQTFQGRVSMTRDRSLT
-FT                       TAFMKMPRLRSDDTALYFCA"
-FT   L-REGION            1..57
-FT                       /translation="MDWTWRILFLVAAATGAHS"
-FT   V-D-J-C-REGION      58..>440
-FT                       /partial
-FT                       /translation="HVQLVQSGPEVKKPGASVRVSCKTSGYTFIDYFIHWVRQAP
-FT                       GQGLEWLGWINPYSGDTNCAQTFQGRVSMTRDRSLTTAFMKMPRLRSDDTALYFC
-FT                       ARGLQDFTLDSWGQGTLVVVSSASPTSPKVF"
-FT   INIT-CODON          1..3
-FT   V-D-J-REGION        58..411
-FT                       /translation="HVQLVQSGPEVKKPGASVRVSCKTSGYTFIDYFIHWVRQAP
-FT                       GQGLEWLGWINPYSGDTNCAQTFQGRVSMTRDRSLTTAFMKMPRLRSDDTALYFC
-FT                       ARGLQDFTLDSWGQGTLVVVSS"
-FT                       /CDR_length="[8.8.11]"
-FT                       /FR_length="[25.17.38.11]"
-FT   V-REGION            58..350
-FT                       /translation="HVQLVQSGPEVKKPGASVRVSCKTSGYTFIDYFIHWVRQAP
-FT                       GQGLEWLGWINPYSGDTNCAQTFQGRVSMTRDRSLTTAFMKMPRLRSDDTALYFC
-FT                       A"
-FT                       /IMGT_allele="IGHV1-2*02 or IGHV1-2*04"
-FT                       /IMGT_gene="IGHV1-2"
-FT                       /Videntity="87,03% (255/293 nt)"
-FT   FR1-IMGT            58..132
-FT                       /translation="HVQLVQSGPEVKKPGASVRVSCKTS"
-FT                       /AA_IMGT="AA 1 to 26, AA 10 is missing"
-FT   1st-CYS             121..123
-FT   CDR1-IMGT           133..156
-FT                       /translation="GYTFIDYF"
-FT                       /AA_IMGT="AA 27 to 38, AA 31, 32, 33 and 34 are 
-FT                       missing"
-FT   FR2-IMGT            157..207
-FT                       /translation="IHWVRQAPGQGLEWLGW"
-FT                       /AA_IMGT="AA 39 to 55"
-FT   CONSERVED-TRP       163..165
-FT   CDR2-IMGT           208..231
-FT                       /translation="INPYSGDT"
-FT                       /AA_IMGT="AA 56 to 65, AA 60 and 61 are missing"
-FT   FR3-IMGT            232..345
-FT                       /translation="NCAQTFQGRVSMTRDRSLTTAFMKMPRLRSDDTALYFC"
-FT                       /AA_IMGT="AA 66 to 104, AA 73 is missing"
-FT   2nd-CYS             343..345
-FT   CDR3-IMGT           346..378
-FT                       /translation="ARGLQDFTLDS"
-FT                       /AA_IMGT="AA 105 to 117, AA 111 and 112 are missing"
-FT   JUNCTION            343..381
-FT                       /translation="CARGLQDFTLDSW"
-FT                       /in_frame
-FT   3'V-REGION          343..350
-FT                       /translation="CA"
-FT   (N-D)-J-REGION      351..411
-FT                       /codon_start=2
-FT                       /translation="GLQDFTLDSWGQGTLVVVSS"
-FT   (N-D)-REGION        351..370
-FT                       /codon_start=2
-FT                       /translation="GLQDFT"
-FT   N1-REGION           351..354
-FT                       /codon_start=2
-FT   D-REGION            355..363
-FT                       /translation="LQD"
-FT                       /IMGT_allele="IGHD2-2*02"
-FT                       /IMGT_gene="IGHD2-2"
-FT   N2-REGION           364..370
-FT                       /translation="FT"
-FT   5'J-REGION          371..381
-FT                       /codon_start=3
-FT                       /translation="DSW"
-FT   J-REGION            371..411
-FT                       /codon_start=3
-FT                       /translation="DSWGQGTLVVVSS"
-FT                       /IMGT_allele="IGHJ4*02"
-FT                       /IMGT_gene="IGHJ4"
-FT   J-TRP               379..381
-FT   FR4-IMGT            379..411
-FT                       /translation="WGQGTLVVVSS"
-FT                       /AA_IMGT="AA 118 to 128"
-FT   C-REGION            412..>440
-FT                       /partial
-FT                       /translation="ASPTSPKVF"
-FT                       /IMGT_allele="IGHA1*01 or IGHA2*01 or IGHA2*02 or 
-FT                       IGHA2*03"
-FT                       /IMGT_gene="IGHA1 or IGHA2"
-XX
-SQ   Sequence 440 BP; 95 A; 128 C; 118 G; 99 T; 0 other;
-     atggactgga cctggaggat cctcttcttg gtggcagcag ccacaggagc ccactcccat        60
-     gtgcaactgg tgcagtctgg gcctgaggtg aaaaagcctg gggcctcagt gagagtctcc       120
-     tgcaagactt ctggatacac cttcatcgac tattttatac actgggtgcg acaggcccct       180
-     ggacaagggc ttgagtggct gggatggatc aacccttaca gtggtgacac aaactgtgca       240
-     cagacttttc agggccgggt ctccatgacc cgtgacaggt ccctcaccac agcctttatg       300
-     aaaatgccta gactgagatc tgacgacacg gccttatatt tctgtgcaag gggactgcaa       360
-     gactttaccc ttgactcttg gggccaggga accctggtcg tcgtctcctc agcatccccg       420
-     accagcccca aggtcttccc                                                   440
-//
-ID   AF067420; SV 1; linear; cDNA; STD; HUM; 1651 BP.
-XX
-AC   AF067420;
-XX
-DT   22-SEP-1998 (Rel. 199839-2, arrived in LIGM-DB)
-DT   15-JUN-2024 (Rel. 202424-6, Last updated, Version 17)
-XX
-DE   Homo sapiens SNC73 protein (SNC73) mRNA, complete cds.
-XX
-KW   antigen receptor; Immunoglobulin superfamily (IgSF); immunoglobulin (IG);
-KW   IG-Heavy; IG-Heavy-Alpha; constant; IG-Heavy-Alpha-1-IGHA1; variable;
-KW   diversity; joining; regular; cDNA; undefined; rearranged; productive;
-KW   L-V-D-J-C-sequence.
-XX
-OS   Homo sapiens (human)
-OC   cellular organisms; Eukaryota; Opisthokonta; Metazoa; Eumetazoa; Bilateria;
-OC   Deuterostomia; Chordata; Craniata; Vertebrata; Gnathostomata; Teleostomi;
-OC   Euteleostomi; Sarcopterygii; Dipnotetrapodomorpha; Tetrapoda; Amniota;
-OC   Mammalia; Theria; Eutheria; Boreoeutheria; Euarchontoglires; Primates;
-OC   Haplorrhini; Simiiformes; Catarrhini; Hominoidea; Hominidae; Homininae;
-OC   Homo; Homo sapiens.
-XX
-RN   [1]
-RP   1-1651
-RA   Zheng S., Cao J., Cao W., Cai X., Geng L.;
-RT   "Identification and characterization of SNC73, a gene which is
-RT   down-regulated in colorectal cancer";
-RL   Unpublished.
-XX
-RN   [2]
-RP   1-1651
-RA   Zheng S., Cao J., Cao W., Cai X., Geng L.;
-RT   ;
-RL   Submitted (19-MAY-1998) to the INSDC.
-RL   Cancer Institute, Zhejiang Medical University, 68 Jiefang Road, Hangzhou,
-RL   Zhejiang 310009, P. R. China
-XX
-RN   [3]
-RC   Sequence update by submitter
-RP   1-1651
-RA   Zheng S., Cao J., Cao W., Cai X., Geng L.;
-RT   ;
-RL   Submitted (09-JUN-1998) to the INSDC.
-RL   Cancer Institute, Zhejiang Medical University, 68 Jiefang Road, Hangzhou,
-RL   Zhejiang 310009, P. R. China
-XX
-DR   EuropePMC; PMC2915949; 20602808.
-DR   EuropePMC; PMC4147138; 17511028.
-DR   EuropePMC; PMC4725172; 16437709.
-DR   MD5; cbacd0f1b767e3829eada0e01a2c10e2.
-XX
-CC   IMGT/LIGM-DB annotation level: by annotators
-CC
-CC   On Jun 10, 1998 this sequence version replaced gi:3192828.
-XX
-FH   Key                 Location/Qualifiers
-FH
-FT   L-V-D-J-C-SEQUENCE  1..1651
-FT                       /db_xref="taxon:9606"
-FT                       /mol_type="cDNA"
-FT                       /organism="Homo sapiens"
-FT                       /productive
-FT   L-V-D-J-C-REGION    66..1547
-FT                       /translation="MTEFGLSWVFLVAIFKGVQCEVQLVESGGDLVQPGGSLRLS
-FT                       CAASGFTFSSYAMHWVRQAPGKGLKYVSGISSNGRRTYYANSVKGRFTISRDNSK
-FT                       NTLYLQMGSLRAEDMAVYYCVSGGIYDSSGPFDYWGQGTLVTVSSASPTSPKVFP
-FT                       LSLCSTQPDGNVVIACLVQGFFPQEPLSVTWSESGQGVTARNFPPSQDASGDLYT
-FT                       TSSQLTLPATQCLAGKSVTCHVKHYTNPSQDVTVPCPVPSTPPTPSPSTPPTPSP
-FT                       SCCHPRLSLHRPALEDLLLGSEANLTCTLTGLRDASGVTFTWTPSSGKSAVQGPP
-FT                       ERDLCGCYSVSSVLPGCAEPWNHGKTFTCTAAYPESKTPLTATLSKSGNTFRPEV
-FT                       HLLPPPSEELALNELVTLTCLARGFSPKDVLVRWLQGSQELPREKYLTWASRQEP
-FT                       SQGTTTFAVTSILRVAAEDWKKGDTFSCMVGHEALPLAFTQKTIDRLAGKPTHVN
-FT                       VSVVMAEVDGTCY"
-FT   5'UTR               1..65
-FT   L-V-D-J-REGION      66..488
-FT                       /translation="MTEFGLSWVFLVAIFKGVQCEVQLVESGGDLVQPGGSLRLS
-FT                       CAASGFTFSSYAMHWVRQAPGKGLKYVSGISSNGRRTYYANSVKGRFTISRDNSK
-FT                       NTLYLQMGSLRAEDMAVYYCVSGGIYDSSGPFDYWGQGTLVTVSS"
-FT   L-V-D-REGION        66..443
-FT                       /translation="MTEFGLSWVFLVAIFKGVQCEVQLVESGGDLVQPGGSLRLS
-FT                       CAASGFTFSSYAMHWVRQAPGKGLKYVSGISSNGRRTYYANSVKGRFTISRDNSK
-FT                       NTLYLQMGSLRAEDMAVYYCVSGGIYDSSG"
-FT   L-V-REGION          66..414
-FT                       /translation="MTEFGLSWVFLVAIFKGVQCEVQLVESGGDLVQPGGSLRLS
-FT                       CAASGFTFSSYAMHWVRQAPGKGLKYVSGISSNGRRTYYANSVKGRFTISRDNSK
-FT                       NTLYLQMGSLRAEDMAVYYC"
-FT   L-REGION            66..125
-FT                       /translation="MTEFGLSWVFLVAIFKGVQC"
-FT   V-D-J-C-REGION      126..1547
-FT                       /translation="EVQLVESGGDLVQPGGSLRLSCAASGFTFSSYAMHWVRQAP
-FT                       GKGLKYVSGISSNGRRTYYANSVKGRFTISRDNSKNTLYLQMGSLRAEDMAVYYC
-FT                       VSGGIYDSSGPFDYWGQGTLVTVSSASPTSPKVFPLSLCSTQPDGNVVIACLVQG
-FT                       FFPQEPLSVTWSESGQGVTARNFPPSQDASGDLYTTSSQLTLPATQCLAGKSVTC
-FT                       HVKHYTNPSQDVTVPCPVPSTPPTPSPSTPPTPSPSCCHPRLSLHRPALEDLLLG
-FT                       SEANLTCTLTGLRDASGVTFTWTPSSGKSAVQGPPERDLCGCYSVSSVLPGCAEP
-FT                       WNHGKTFTCTAAYPESKTPLTATLSKSGNTFRPEVHLLPPPSEELALNELVTLTC
-FT                       LARGFSPKDVLVRWLQGSQELPREKYLTWASRQEPSQGTTTFAVTSILRVAAEDW
-FT                       KKGDTFSCMVGHEALPLAFTQKTIDRLAGKPTHVNVSVVMAEVDGTCY"
-FT   INIT-CODON          66..68
-FT   V-D-J-REGION        126..488
-FT                       /translation="EVQLVESGGDLVQPGGSLRLSCAASGFTFSSYAMHWVRQAP
-FT                       GKGLKYVSGISSNGRRTYYANSVKGRFTISRDNSKNTLYLQMGSLRAEDMAVYYC
-FT                       VSGGIYDSSGPFDYWGQGTLVTVSS"
-FT                       /CDR_length="[8.8.14]"
-FT                       /FR_length="[25.17.38.11]"
-FT   V-REGION            126..414
-FT                       /translation="EVQLVESGGDLVQPGGSLRLSCAASGFTFSSYAMHWVRQAP
-FT                       GKGLKYVSGISSNGRRTYYANSVKGRFTISRDNSKNTLYLQMGSLRAEDMAVYYC
-FT                       "
-FT                       /functional
-FT                       /IMGT_allele="IGHV3-64*01"
-FT                       /IMGT_gene="IGHV3-64"
-FT                       /Videntity="97,23% (281/289 nt)"
-FT   FR1-IMGT            126..200
-FT                       /translation="EVQLVESGGDLVQPGGSLRLSCAAS"
-FT                       /AA_IMGT="AA 1 to 26, AA 10 is missing"
-FT   1st-CYS             189..191
-FT   CDR1-IMGT           201..224
-FT                       /translation="GFTFSSYA"
-FT                       /AA_IMGT="AA 27 to 38, AA 31, 32, 33 and 34 are 
-FT                       missing"
-FT   FR2-IMGT            225..275
-FT                       /translation="MHWVRQAPGKGLKYVSG"
-FT                       /AA_IMGT="AA 39 to 55"
-FT   CONSERVED-TRP       231..233
-FT   CDR2-IMGT           276..299
-FT                       /translation="ISSNGRRT"
-FT                       /AA_IMGT="AA 56 to 65, AA 60 and 61 are missing"
-FT   FR3-IMGT            300..413
-FT                       /translation="YYANSVKGRFTISRDNSKNTLYLQMGSLRAEDMAVYYC"
-FT                       /AA_IMGT="AA 66 to 104, AA 73 is missing"
-FT   2nd-CYS             411..413
-FT   CDR3-IMGT           414..455
-FT                       /translation="VSGGIYDSSGPFDY"
-FT                       /AA_IMGT="AA 105 to 117, AA 112.1 is added"
-FT   JUNCTION            411..458
-FT                       /translation="CVSGGIYDSSGPFDYW"
-FT                       /in_frame
-FT   3'V-REGION          411..414
-FT                       /translation="C"
-FT   (N-D)-J-REGION      415..488
-FT                       /codon_start=3
-FT                       /translation="SGGIYDSSGPFDYWGQGTLVTVSS"
-FT   (N-D)-REGION        415..445
-FT                       /codon_start=3
-FT                       /translation="SGGIYDSSG"
-FT   N1-REGION           415..427
-FT                       /codon_start=3
-FT                       /translation="SGG"
-FT   D-J-REGION          428..488
-FT                       /codon_start=2
-FT                       /translation="YDSSGPFDYWGQGTLVTVSS"
-FT   D-REGION            428..443
-FT                       /codon_start=2
-FT                       /translation="YDSSG"
-FT                       /functional
-FT                       /IMGT_allele="IGHD3-22*01"
-FT                       /IMGT_gene="IGHD3-22"
-FT   N2-REGION           444..445
-FT   5'J-REGION          446..458
-FT                       /codon_start=2
-FT                       /translation="FDYW"
-FT   J-REGION            446..488
-FT                       /codon_start=2
-FT                       /translation="FDYWGQGTLVTVSS"
-FT                       /functional
-FT                       /IMGT_allele="IGHJ4*02"
-FT                       /IMGT_gene="IGHJ4"
-FT   J-TRP               456..458
-FT   FR4-IMGT            456..488
-FT                       /translation="WGQGTLVTVSS"
-FT                       /AA_IMGT="AA 118 to 128"
-FT   C-REGION            490..1547
-FT                       /functional
-FT                       /IMGT_allele="IGHA1*01"
-FT                       /IMGT_gene="IGHA1"
-FT   CH1                 490..795
-FT   SPLICE-FIRST-CODON  489..491
-FT                       /splicing-frame="sf1"
-FT   H-CH2               796..1155
-FT   SPLICE-FIRST-CODON  795..797
-FT                       /splicing-frame="sf1"
-FT   H                   796..851
-FT                       /translation="FPQLHLPHLPQLHLPHLP"
-FT                       /IMGT_note="putative limit of the hinge"
-FT   CH2                 852..1155
-FT                       /translation="CCHPRLSLHRPALEDLLLGSEANLTCTLTGLRDASGVTFTW
-FT                       TPSSGKSAVQGPPERDLCGCYSVSSVLPGCAEPWNHGKTFTCTAAYPESKTPLTA
-FT                       TLSKS"
-FT   CH3-CHS             1156..1547
-FT   SPLICE-FIRST-CODON  1155..1156
-FT                       /splicing-frame="sf1"
-FT   CH3                 1156..1487
-FT   CHS                 1488..1547
-FT                       /translation="GKPTHVNVSVVMAEVDGTCY"
-FT   INT-DONOR-SPLICE    1488..1490
-FT                       /IMGT_note="for complete translation nucleotide G at 
-FT                       position 1488 has been included in CHS"
-FT   3'UTR               1548..1651
-FT   STOP-CODON          1548..1550
-XX
-SQ   Sequence 1651 BP; 376 A; 516 C; 443 G; 316 T; 0 other;
-     ggagcccccg ccctgggatt cccaggtgtt ttcatttggt gatcagcact gaacacagaa        60
-     gagtcatgac ggagtttggg ctgagctggg ttttccttgt tgctattttt aaaggtgtcc       120
-     agtgtgaggt gcagctggtg gagtctgggg gagacttggt ccagcctggg gggtccctga       180
-     gactctcctg tgcagcctct ggattcacct tcagtagtta tgctatgcac tgggtccgcc       240
-     aggctccagg gaagggactg aaatatgttt caggtattag tagtaatggg cgtagaacat       300
-     attatgcaaa ttctgtgaag ggcagattca ccatctccag agacaattcc aagaacacgt       360
-     tgtatcttca aatgggcagc ctgagagctg aggacatggc tgtgtattac tgtgtgtccg       420
-     ggggaatcta tgatagtagt ggtccctttg actactgggg ccagggaacc ctggtcaccg       480
-     tctcctcagc atccccgacc agccccaagg tcttcccgct gagcctctgc agcacccagc       540
-     cagatgggaa cgtggtcatc gcctgcctgg tccagggctt cttcccccag gagccactca       600
-     gtgtgacctg gagcgaaagc ggacagggcg tgaccgccag aaacttccca cccagccagg       660
-     atgcctccgg ggacctgtac accacgagca gccagctgac cctgccggcc acacagtgcc       720
-     tagccggcaa gtccgtgaca tgccacgtga agcactacac gaatcccagc caggatgtga       780
-     ctgtgccctg cccagttccc tcaactccac ctaccccatc tccctcaact ccacctaccc       840
-     catctccctc atgctgccac ccccgactgt cactgcaccg accggccctc gaggacctgc       900
-     tcttaggttc agaagcgaac ctcacgtgca cactgaccgg cctgagagat gcctcaggtg       960
-     tcaccttcac ctggacgccc tcaagtggga agagcgctgt tcaaggacca cctgagcgtg      1020
-     acctctgtgg ctgctacagc gtgtccagtg tcctgccggg ctgtgccgag ccatggaacc      1080
-     atgggaagac cttcacttgc actgctgcct accccgagtc caagaccccg ctaaccgcca      1140
-     ccctctcaaa atccggaaac acattccggc ccgaggtcca cctgctgccg ccgccgtcgg      1200
-     aggagctggc cctgaacgag ctggtgacgc tgacgtgcct ggcacgcggc ttcagcccca      1260
-     aggacgtgct ggttcgctgg ctgcaggggt cacaggagct gccccgcgag aagtacctga      1320
-     cttgggcatc ccggcaggag cccagccagg gcaccaccac cttcgctgtg accagcatac      1380
-     tgcgcgtggc agccgaggac tggaagaagg gggacacctt ctcctgcatg gtgggccacg      1440
-     aggccctgcc gctggccttc acacagaaga ccatcgaccg cttggcgggt aaacccaccc      1500
-     atgtcaatgt gtctgttgtc atggcggagg tggacggcac ctgctactga gccgcccgcc      1560
-     tgtccccacc cctgaataaa ctccatgctc ccccaaaaaa aaaaaaaaaa aaaaaaaaaa      1620
-     aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa a                                     1651
-//
-ID   AF103054; SV 1; linear; cDNA; STD; HUM; 362 BP.
-XX
-AC   AF103054;
-XX
-DT   15-OCT-2001 (Rel. 200142-1, arrived in LIGM-DB)
-DT   15-JUN-2024 (Rel. 202424-6, Last updated, Version 8)
-XX
-DE   Homo sapiens isolate donor D clone D19 immunoglobulin heavy chain variable
-DE   region mRNA, partial cds.
-XX
-KW   antigen receptor; Immunoglobulin superfamily (IgSF); immunoglobulin (IG);
-KW   IG-Heavy; constant; variable; diversity; joining; regular; cDNA; undefined;
-KW   rearranged; productive; L-V-D-J-C-sequence.
-XX
-OS   Homo sapiens (human)
-OC   cellular organisms; Eukaryota; Opisthokonta; Metazoa; Eumetazoa; Bilateria;
-OC   Deuterostomia; Chordata; Craniata; Vertebrata; Gnathostomata; Teleostomi;
-OC   Euteleostomi; Sarcopterygii; Dipnotetrapodomorpha; Tetrapoda; Amniota;
-OC   Mammalia; Theria; Eutheria; Boreoeutheria; Euarchontoglires; Primates;
-OC   Haplorrhini; Simiiformes; Catarrhini; Hominoidea; Hominidae; Homininae;
-OC   Homo; Homo sapiens.
-XX
-RN   [1]
-RC   Contact ncbi-contacts@bcm.tmc.edu for more information.
-RP   1-362
-RA   Rat Genome Sequencing Consortium;
-RT   ;
-RL   Submitted (11-JUL-2003) to the INSDC.
-RL   Human Genome Sequencing Center, Department of Molecular and Human Genetics,
-RL   Baylor College of Medicine, One Baylor Plaza, Houston, TX 77030, USA
-XX
-RN   [2]
-RP   1-362
-RA   Mage R.G., Sehgal D., Schiaffella E.;
-RT   ;
-RL   Submitted (18-JUL-1997) to the INSDC.
-RL   Laboratory of Immunology, National Institute of Allergy and Infectious
-RL   Disease, 10 Center Drive - MSC 1892, Bethesda, MD 20892, USA
-XX
-DR   MD5; ad8ca0f44bc0e093f8c4965bca0e4a3e.
-XX
-CC   IMGT/LIGM-DB annotation level: by annotators
-XX
-FH   Key                 Location/Qualifiers
-FH
-FT   L-V-D-J-C-SEQUENCE  <1..>362
-FT                       /partial
-FT                       /cell_type="B cell"
-FT                       /clone="D19"
-FT                       /db_xref="taxon:9606"
-FT                       /isolate="donor D"
-FT                       /organism="Homo sapiens"
-FT                       /productive
-FT                       /tissue_type="peripheral blood"
-FT   V-D-J-C-REGION      <1..>362
-FT                       /partial
-FT                       /translation="LVKPSETLSLTCTVSGGSISPYSWTWIRQSPGKGLEWIGHI
-FT                       YYSGSTNYNPSLKSRVTILVDTSKNQLSLNLSSVNAADTAVYYCARGERPQLVKG
-FT                       RDWFDPWGQGILVTVSSAPPRPIV"
-FT                       /product="immunoglobulin heavy chain variable region"
-FT                       /protein_id="AAD16495.1"
-FT   V-D-J-REGION        <1..339
-FT                       /partial
-FT                       /translation="LVKPSETLSLTCTVSGGSISPYSWTWIRQSPGKGLEWIGHI
-FT                       YYSGSTNYNPSLKSRVTILVDTSKNQLSLNLSSVNAADTAVYYCARGERPQLVKG
-FT                       RDWFDPWGQGILVTVSS"
-FT                       /CDR_length="[8.7.17]"
-FT                       /FR_length="[X.17.38.11]"
-FT   V-REGION            <1..262
-FT                       /partial
-FT                       /translation="LVKPSETLSLTCTVSGGSISPYSWTWIRQSPGKGLEWIGHI
-FT                       YYSGSTNYNPSLKSRVTILVDTSKNQLSLNLSSVNAADTAVYYCAR"
-FT                       /IMGT_allele="IGHV4-59*01"
-FT                       /IMGT_gene="IGHV4-59"
-FT                       /Videntity="94,66% (248/262 nt)"
-FT   FR1-IMGT            <1..45
-FT                       /partial
-FT                       /translation="LVKPSETLSLTCTVS"
-FT                       /AA_IMGT="AA 12 to 26"
-FT   1st-CYS             34..36
-FT   CDR1-IMGT           46..69
-FT                       /translation="GGSISPYS"
-FT                       /AA_IMGT="AA 27 to 38, AA 31, 32, 33 and 34 are 
-FT                       missing"
-FT   FR2-IMGT            70..120
-FT                       /translation="WTWIRQSPGKGLEWIGH"
-FT                       /AA_IMGT="AA 39 to 55"
-FT   CONSERVED-TRP       76..78
-FT   CDR2-IMGT           121..141
-FT                       /translation="IYYSGST"
-FT                       /AA_IMGT="AA 56 to 65, AA 60, 61 and 62 are missing"
-FT   FR3-IMGT            142..255
-FT                       /translation="NYNPSLKSRVTILVDTSKNQLSLNLSSVNAADTAVYYC"
-FT                       /AA_IMGT="AA 66 to 104, AA 73 is missing"
-FT   2nd-CYS             253..255
-FT   CDR3-IMGT           256..306
-FT                       /translation="ARGERPQLVKGRDWFDP"
-FT                       /AA_IMGT="AA 105 to 117, AA 112.1, 111.1, 112.2 and 
-FT                       111.2 are added"
-FT   JUNCTION            253..309
-FT                       /translation="CARGERPQLVKGRDWFDPW"
-FT                       /in_frame
-FT   3'V-REGION          253..262
-FT                       /translation="CAR"
-FT   (N-D)-J-REGION      263..339
-FT                       /codon_start=3
-FT                       /translation="ERPQLVKGRDWFDPWGQGILVTVSS"
-FT   (N-D)-REGION        263..292
-FT                       /codon_start=3
-FT                       /translation="ERPQLVKGR"
-FT   N1-REGION           263..269
-FT                       /codon_start=3
-FT                       /translation="E"
-FT   D-REGION            270..281
-FT                       /codon_start=2
-FT                       /translation="PQL"
-FT                       /IMGT_allele="IGHD6-13*01"
-FT                       /IMGT_gene="IGHD6-13"
-FT   N2-REGION           282..292
-FT                       /codon_start=2
-FT                       /translation="KGR"
-FT   5'J-REGION          293..309
-FT                       /codon_start=3
-FT                       /translation="WFDPW"
-FT   J-REGION            293..339
-FT                       /codon_start=3
-FT                       /translation="WFDPWGQGILVTVSS"
-FT                       /IMGT_allele="IGHJ5*02"
-FT                       /IMGT_gene="IGHJ5"
-FT   J-TRP               307..309
-FT   FR4-IMGT            307..339
-FT                       /translation="WGQGILVTVSS"
-FT                       /AA_IMGT="AA 118 to 128"
-FT   C-REGION            340..>362
-FT                       /partial
-FT                       /translation="APPRPIV"
-FT                       /IMGT_allele="IGHA1*01 or IGHA2*01 or IGHA2*02 or 
-FT                       IGHA2*03"
-FT                       /IMGT_gene="IGHA1 or IGHA2"
-XX
-SQ   Sequence 362 BP; 77 A; 110 C; 98 G; 77 T; 0 other;
-     ctggtgaagc cttcggagac cctgtccctc acctgcactg tctccggtgg ctccatcagt        60
-     ccttactcct ggacctggat ccggcagtcc ccagggaagg gactggagtg gattggccat       120
-     atctattata gtgggagcac caactacaac ccctccctca agagtcgagt caccatatta       180
-     gtagacacgt ccaagaacca gctctccctg aatctgagct ctgtgaatgc tgcggacacg       240
-     gccgtgtatt actgtgcgag aggagaaagg ccgcagctgg tcaaagggag ggactggttc       300
-     gacccctggg gccagggaat tctggtcacc gtctcctcag ctccaccaag gcccatcgtc       360
-     tt                                                                      362
-//
-ID   AF184762; SV 1; linear; cDNA; STD; HUM; 471 BP.
-XX
-AC   AF184762;
-XX
-DT   06-DEC-1999 (Rel. 199949-1, arrived in LIGM-DB)
-DT   15-JUN-2024 (Rel. 202424-6, Last updated, Version 6)
-XX
-DE   Homo sapiens IgA1 heavy chain mRNA, partial cds.
-XX
-KW   antigen receptor; Immunoglobulin superfamily (IgSF); immunoglobulin (IG);
-KW   IG-Heavy; IG-Heavy-Alpha; constant; IG-Heavy-Alpha-1-IGHA1; variable;
-KW   diversity; joining; regular; cDNA; undefined; rearranged; productive;
-KW   L-V-D-J-C-sequence.
-XX
-OS   Homo sapiens (human)
-OC   cellular organisms; Eukaryota; Opisthokonta; Metazoa; Eumetazoa; Bilateria;
-OC   Deuterostomia; Chordata; Craniata; Vertebrata; Gnathostomata; Teleostomi;
-OC   Euteleostomi; Sarcopterygii; Dipnotetrapodomorpha; Tetrapoda; Amniota;
-OC   Mammalia; Theria; Eutheria; Boreoeutheria; Euarchontoglires; Primates;
-OC   Haplorrhini; Simiiformes; Catarrhini; Hominoidea; Hominidae; Homininae;
-OC   Homo; Homo sapiens.
-XX
-RN   [1]
-RP   1-471
-RA   Kitagawa Y.;
-RT   ;
-RL   Submitted (17-OCT-2000) to the INSDC.
-RL   Yoshichika Kitagawa, Akita Prefectural University, Biotechnology Institute;
-RL   Minami 2-2, Ogata, Akita 010-0444, Japan
-RL   (E-mail:kitagawa@agri.akita-pu.ac.jp, URL:www.akita-pu.ac.jp/,
-RL   Tel:81-185-45-2026(ex.400), Fax:81-185-45-2678)
-XX
-RN   [2]
-RP   1-471
-RA   Lucero J.E., Rosenberg G.H., Miller R.D.;
-RT   ;
-RL   Submitted (23-FEB-1998) to the INSDC.
-RL   Biology, University of New Mexico, Albuquerque, NM 87110, USA
-XX
-DR   MD5; efdedc448d28c5d55234252f3d51cc55.
-XX
-CC   IMGT/LIGM-DB annotation level: automatic
-XX
-FH   Key                 Location/Qualifiers
-FH
-FT   L-V-D-J-C-SEQUENCE  <1..>471
-FT                       /partial
-FT                       /chromosome="14"
-FT                       /db_xref="taxon:9606"
-FT                       /map="14q32.33"
-FT                       /organism="Homo sapiens"
-FT                       /productive
-FT   L-V-D-J-C-REGION    1..>471
-FT                       /partial
-FT                       /translation="MEFGLSWVFLVAILKGVHCEVQLVESGGGLVQPGGSLKLSC
-FT                       AASGFTLSGSNVHWVRQASGKGLEWVGRIKRNAESDATAYAASMRGRLTISRDDS
-FT                       KNTAFLQMNSLKSDDTAMYYCVIRGDVYNRQWGQGTLVTVSSASPTSPKVFPLSL
-FT                       CSTQPD"
-FT                       /product="IgA1 heavy chain"
-FT                       /protein_id="AAF03879.1"
-FT   L-V-D-J-REGION      1..414
-FT                       /translation="MEFGLSWVFLVAILKGVHCEVQLVESGGGLVQPGGSLKLSC
-FT                       AASGFTLSGSNVHWVRQASGKGLEWVGRIKRNAESDATAYAASMRGRLTISRDDS
-FT                       KNTAFLQMNSLKSDDTAMYYCVIRGDVYNRQWGQGTLVTVSS"
-FT   L-V-D-REGION        1..369
-FT                       /translation="MEFGLSWVFLVAILKGVHCEVQLVESGGGLVQPGGSLKLSC
-FT                       AASGFTLSGSNVHWVRQASGKGLEWVGRIKRNAESDATAYAASMRGRLTISRDDS
-FT                       KNTAFLQMNSLKSDDTAMYYCVIRGDV"
-FT   L-V-REGION          1..351
-FT                       /translation="MEFGLSWVFLVAILKGVHCEVQLVESGGGLVQPGGSLKLSC
-FT                       AASGFTLSGSNVHWVRQASGKGLEWVGRIKRNAESDATAYAASMRGRLTISRDDS
-FT                       KNTAFLQMNSLKSDDTAMYYC"
-FT   L-REGION            1..57
-FT                       /translation="MEFGLSWVFLVAILKGVHC"
-FT   V-D-J-C-REGION      58..>471
-FT                       /partial
-FT                       /translation="EVQLVESGGGLVQPGGSLKLSCAASGFTLSGSNVHWVRQAS
-FT                       GKGLEWVGRIKRNAESDATAYAASMRGRLTISRDDSKNTAFLQMNSLKSDDTAMY
-FT                       YCVIRGDVYNRQWGQGTLVTVSSASPTSPKVFPLSLCSTQPD"
-FT   INIT-CODON          1..3
-FT   V-D-J-REGION        58..414
-FT                       /translation="EVQLVESGGGLVQPGGSLKLSCAASGFTLSGSNVHWVRQAS
-FT                       GKGLEWVGRIKRNAESDATAYAASMRGRLTISRDDSKNTAFLQMNSLKSDDTAMY
-FT                       YCVIRGDVYNRQWGQGTLVTVSS"
-FT                       /CDR_length="[8.10.10]"
-FT                       /FR_length="[25.17.38.11]"
-FT   V-REGION            58..351
-FT                       /translation="EVQLVESGGGLVQPGGSLKLSCAASGFTLSGSNVHWVRQAS
-FT                       GKGLEWVGRIKRNAESDATAYAASMRGRLTISRDDSKNTAFLQMNSLKSDDTAMY
-FT                       YC"
-FT                       /IMGT_allele="IGHV3-73*01"
-FT                       /IMGT_gene="IGHV3-73"
-FT                       /Videntity="91,50% (269/294 nt)"
-FT   FR1-IMGT            58..132
-FT                       /translation="EVQLVESGGGLVQPGGSLKLSCAAS"
-FT                       /AA_IMGT="AA 1 to 26, AA 10 is missing"
-FT   1st-CYS             121..123
-FT   CDR1-IMGT           133..156
-FT                       /translation="GFTLSGSN"
-FT                       /AA_IMGT="AA 27 to 38, AA 31, 32, 33 and 34 are 
-FT                       missing"
-FT   FR2-IMGT            157..207
-FT                       /translation="VHWVRQASGKGLEWVGR"
-FT                       /AA_IMGT="AA 39 to 55"
-FT   CONSERVED-TRP       163..165
-FT   CDR2-IMGT           208..237
-FT                       /translation="IKRNAESDAT"
-FT                       /AA_IMGT="AA 56 to 65"
-FT   FR3-IMGT            238..351
-FT                       /translation="AYAASMRGRLTISRDDSKNTAFLQMNSLKSDDTAMYYC"
-FT                       /AA_IMGT="AA 66 to 104, AA 73 is missing"
-FT   2nd-CYS             349..351
-FT   CDR3-IMGT           352..381
-FT                       /translation="VIRGDVYNRQ"
-FT                       /AA_IMGT="AA 105 to 117, AA 110, 111 and 112 are 
-FT                       missing"
-FT   JUNCTION            349..384
-FT                       /translation="CVIRGDVYNRQW"
-FT                       /in_frame
-FT   3'V-REGION          349..351
-FT   (N-D)-REGION        352..378
-FT                       /translation="VIRGDVYNR"
-FT   N1-REGION           352
-FT   D-J-REGION          353..414
-FT                       /codon_start=3
-FT                       /translation="IRGDVYNRQWGQGTLVTVSS"
-FT   D-REGION            353..369
-FT                       /codon_start=3
-FT                       /translation="IRGDV"
-FT                       /IMGT_allele="IGHD3-10*01"
-FT                       /IMGT_gene="IGHD3-10"
-FT   N2-REGION           370..378
-FT                       /translation="YNR"
-FT   5'J-REGION          379..384
-FT                       /translation="QW"
-FT   J-REGION            379..414
-FT                       /translation="QWGQGTLVTVSS"
-FT                       /IMGT_allele="IGHJ1*01"
-FT                       /IMGT_gene="IGHJ1"
-FT                       /IMGT_note="IGHJ4*02 and IGHJ5*02 may be also solution"
-FT   J-TRP               382..384
-FT   FR4-IMGT            382..414
-FT                       /translation="WGQGTLVTVSS"
-FT                       /AA_IMGT="AA 118 to 128"
-FT   C-REGION            415..>471
-FT                       /partial
-FT                       /translation="ASPTSPKVFPLSLCSTQPD"
-FT                       /IMGT_allele="IGHA1*01"
-FT                       /IMGT_gene="IGHA1"
-XX
-SQ   Sequence 471 BP; 100 A; 123 C; 143 G; 105 T; 0 other;
-     atggagtttg ggctgagctg ggttttcctt gttgctattt taaaaggtgt ccactgtgag        60
-     gtgcagctgg tggagtctgg gggaggctta gtccagcctg ggggatccct gaaactctcc       120
-     tgtgcagcct ctgggttcac cctcagtggc tcaaatgtgc actgggtccg ccaggcctcc       180
-     gggaaagggc tggagtgggt tggccgtatc aaaaggaatg ctgagtctga cgcgacagca       240
-     tatgctgcgt cgatgagagg caggctcacc atctccagag atgattcaaa gaacacggcg       300
-     tttctgcaaa tgaacagcct gaaaagcgat gacacggcca tgtattattg tgtgatccgg       360
-     ggagatgttt acaaccgaca gtggggccag ggaaccctgg tcaccgtctc ctcagcatcc       420
-     ccgaccagcc ccaaggtctt cccgctgagc ctctgcagca cccagccaga t                471
-//
-ID   AJ230650; SV 1; linear; cDNA; STD; HUM; 386 BP.
-XX
-AC   AJ230650;
-XX
-DT   28-SEP-1999 (Rel. 199939-2, arrived in LIGM-DB)
-DT   15-JUN-2024 (Rel. 202424-6, Last updated, Version 6)
-XX
-DE   Homo sapiens mRNA for rearranged immunoglobulin A1 heavy chain,
-DE   VH251-D-JH3B-Calpha1, clone ET 75
-XX
-KW   antigen receptor; Immunoglobulin superfamily (IgSF); immunoglobulin (IG);
-KW   IG-Heavy; IG-Heavy-Alpha; constant; IG-Heavy-Alpha-1-IGHA1; variable;
-KW   diversity; joining; regular; cDNA; undefined; rearranged; productive;
-KW   L-V-D-J-C-sequence.
-XX
-OS   Homo sapiens (human)
-OC   cellular organisms; Eukaryota; Opisthokonta; Metazoa; Eumetazoa; Bilateria;
-OC   Deuterostomia; Chordata; Craniata; Vertebrata; Gnathostomata; Teleostomi;
-OC   Euteleostomi; Sarcopterygii; Dipnotetrapodomorpha; Tetrapoda; Amniota;
-OC   Mammalia; Theria; Eutheria; Boreoeutheria; Euarchontoglires; Primates;
-OC   Haplorrhini; Simiiformes; Catarrhini; Hominoidea; Hominidae; Homininae;
-OC   Homo; Homo sapiens.
-XX
-RN   [2]
-RP   1-386
-RA   Hein W.R.;
-RT   ;
-RL   Submitted (11-DEC-1997) to the INSDC.
-RL   Basel Institute for Immunology, Grenzacherstrasse 487, Basel Postfach
-RL   CH-4005, Switzerland
-XX
-RN   [3]
-RP   1-386
-RX   DOI; 10.1046/j.1365-2567.1999.00843.x.
-RX   PUBMED; 10457207.
-RA   Boursier L., Dunn-Walters D.K., Spencer J.;
-RT   "Characteristics of IgVH genes used by human intestinal plasma cells from
-RT   childhood";
-RL   Immunology 97(4):558-564(1999).
-XX
-DR   MD5; 1fedea37578020168077c359aa377ec5.
-XX
-CC   IMGT/LIGM-DB annotation level: automatic
-XX
-FH   Key                 Location/Qualifiers
-FH
-FT   L-V-D-J-C-SEQUENCE  <1..>386
-FT                       /partial
-FT                       /cell_type="adult duodenal lamina propria plasma cell"
-FT                       /chromosome="14"
-FT                       /clone="ET 75"
-FT                       /db_xref="taxon:9606"
-FT                       /isolate="patient LSm"
-FT                       /map="q32.33"
-FT                       /organism="Homo sapiens"
-FT                       /productive
-FT   V-D-J-C-REGION      <1..>386
-FT                       /partial
-FT                       /codon_start=2
-FT                       /translation="ISCKGFGYNFNTYWIGWVRQLPGKGLEYMGIIYPGDSDTRY
-FT                       SPSFQGQITISADKSISTAYLQWSSLKASDSAMYYCARRPAGMGPGGAFDIWGQG
-FT                       TMVTVSSASPTSPKVFPLSLCSTQPDGNVVIA"
-FT   V-D-J-REGION        <1..310
-FT                       /partial
-FT                       /codon_start=2
-FT                       /translation="ISCKGFGYNFNTYWIGWVRQLPGKGLEYMGIIYPGDSDTRY
-FT                       SPSFQGQITISADKSISTAYLQWSSLKASDSAMYYCARRPAGMGPGGAFDIWGQG
-FT                       TMVTVSS"
-FT                       /CDR_length="[8.8.15]"
-FT                       /FR_length="[X.17.38.11]"
-FT   V-REGION            <1..239
-FT                       /partial
-FT                       /codon_start=2
-FT                       /translation="ISCKGFGYNFNTYWIGWVRQLPGKGLEYMGIIYPGDSDTRY
-FT                       SPSFQGQITISADKSISTAYLQWSSLKASDSAMYYCAR"
-FT                       /IMGT_allele="IGHV5-51*01 or IGHV5-51*03"
-FT                       /IMGT_gene="IGHV5-51"
-FT                       /Videntity="95,40% (228/239 nt)"
-FT   FR1-IMGT            <1..19
-FT                       /partial
-FT                       /codon_start=2
-FT                       /translation="ISCKGF"
-FT                       /AA_IMGT="AA 20 to 26"
-FT   1st-CYS             8..10
-FT   CDR1-IMGT           20..43
-FT                       /translation="GYNFNTYW"
-FT                       /AA_IMGT="AA 27 to 38, AA 31, 32, 33 and 34 are 
-FT                       missing"
-FT   FR2-IMGT            44..94
-FT                       /translation="IGWVRQLPGKGLEYMGI"
-FT                       /AA_IMGT="AA 39 to 55"
-FT   CONSERVED-TRP       50..52
-FT   CDR2-IMGT           95..118
-FT                       /translation="IYPGDSDT"
-FT                       /AA_IMGT="AA 56 to 65, AA 60 and 61 are missing"
-FT   FR3-IMGT            119..232
-FT                       /translation="RYSPSFQGQITISADKSISTAYLQWSSLKASDSAMYYC"
-FT                       /AA_IMGT="AA 66 to 104, AA 73 is missing"
-FT   2nd-CYS             230..232
-FT   CDR3-IMGT           233..277
-FT                       /translation="ARRPAGMGPGGAFDI"
-FT                       /AA_IMGT="AA 105 to 117, AA 112.1 and 111.1 are added"
-FT   JUNCTION            230..280
-FT                       /translation="CARRPAGMGPGGAFDIW"
-FT                       /in_frame
-FT   3'V-REGION          230..239
-FT                       /translation="CAR"
-FT   (N-D)-REGION        240..265
-FT                       /codon_start=3
-FT                       /translation="PAGMGPGG"
-FT   N1-REGION           240..241
-FT   D-J-REGION          242..310
-FT                       /translation="PAGMGPGGAFDIWGQGTMVTVSS"
-FT   D-REGION            242..253
-FT                       /translation="PAGM"
-FT                       /IMGT_allele="IGHD2-2*01"
-FT                       /IMGT_gene="IGHD2-2"
-FT   N2-REGION           254..265
-FT                       /translation="GPGG"
-FT   5'J-REGION          266..280
-FT                       /translation="AFDIW"
-FT   J-REGION            266..310
-FT                       /translation="AFDIWGQGTMVTVSS"
-FT                       /IMGT_allele="IGHJ3*02"
-FT                       /IMGT_gene="IGHJ3"
-FT   J-TRP               278..280
-FT   FR4-IMGT            278..310
-FT                       /translation="WGQGTMVTVSS"
-FT                       /AA_IMGT="AA 118 to 128"
-FT   C-REGION            311..>386
-FT                       /partial
-FT                       /translation="ASPTSPKVFPLSLCSTQPDGNVVIA"
-FT                       /IMGT_allele="IGHA1*01"
-FT                       /IMGT_gene="IGHA1"
-XX
-SQ   Sequence 386 BP; 82 A; 117 C; 106 G; 81 T; 0 other;
-     gatctcctgt aagggttttg gatacaactt taacacctac tggatcggct gggtgcgcca        60
-     gttgcccggg aaaggcctgg agtatatggg aatcatctat cctggtgact ctgataccag       120
-     atacagcccg tccttccaag gccagatcac catctcagcc gacaagtcca tcagcaccgc       180
-     ctacctgcag tggagcagcc tgaaggcctc ggacagtgcc atgtattact gtgcgagacg       240
-     ccccgctggt atgggaccag ggggggcttt tgatatctgg ggccaaggga caatggtcac       300
-     cgtctcttca gcatccccga ccagccccaa ggtcttcccg ctgagcctct gcagcaccca       360
-     gccagatggg aacgtggtca tcgcct                                            386
-//
-ID   AK027379; SV 1; linear; cDNA; STD; HUM; 1605 BP.
-XX
-AC   AK027379;
-XX
-DT   20-SEP-2001 (Rel. 200138-4, arrived in LIGM-DB)
-DT   15-JUN-2024 (Rel. 202424-6, Last updated, Version 8)
-XX
-DE   Homo sapiens cDNA FLJ14473 fis, clone MAMMA1001080, highly similar to Homo
-DE   sapiens SNC73 protein (SNC73) mRNA.
-XX
-KW   antigen receptor; Immunoglobulin superfamily (IgSF); immunoglobulin (IG);
-KW   IG-Heavy; IG-Heavy-Alpha; constant; IG-Heavy-Alpha-1-IGHA1; variable;
-KW   diversity; joining; regular; cDNA; undefined; rearranged; productive;
-KW   L-V-D-J-C-sequence.
-XX
-OS   Homo sapiens (human)
-OC   cellular organisms; Eukaryota; Opisthokonta; Metazoa; Eumetazoa; Bilateria;
-OC   Deuterostomia; Chordata; Craniata; Vertebrata; Gnathostomata; Teleostomi;
-OC   Euteleostomi; Sarcopterygii; Dipnotetrapodomorpha; Tetrapoda; Amniota;
-OC   Mammalia; Theria; Eutheria; Boreoeutheria; Euarchontoglires; Primates;
-OC   Haplorrhini; Simiiformes; Catarrhini; Hominoidea; Hominidae; Homininae;
-OC   Homo; Homo sapiens.
-XX
-RN   [1]
-RP   1-1605
-RA   Isogai T., Otsuki T.;
-RT   ;
-RL   Submitted (10-MAY-2001) to the INSDC.
-RL   Contact:Takao Isogai Helix Research Institute, Genomics Laboratory; 1532-3
-RL   Yana, Kisarazu, Chiba 292-0812, Japan E-mail :flj-cdna@nifty.com
-XX
-RN   [2]
-RX   DOI; 10.1016/S0165-2478(97)00101-6.
-RX   PUBMED; 9373213.
-RA   Fukuoka M., Tokushima M., Koarada S., Sai T., Miyake K., Kimoto M.;
-RT   "Analysis of Vbeta4 T cell receptor CDR3 repertoire in BALB/c and (NZB x
-RT   NZW)F1 mice";
-RL   Immunol. Lett. 59(2):63-69(1997).
-XX
-RN   [3]
-RX   PUBMED; 8645581.
-RA   Okamoto S., Yoshikawa K., Obata Y., Shibuya M., Aoki S., Yoshida J.,
-RA   Takahashi T.;
-RT   "Monoclonal antibody against the fusion junction of a deletion-mutant
-RT   epidermal growth factor receptor";
-RL   Br. J. Cancer 73(11):1366-1372(1996).
-XX
-DR   MD5; 00fd15746b519819f9fea3ce8cf25c44.
-XX
-CC   IMGT/LIGM-DB annotation level: automatic
-CC
-CC   NEDO human cDNA sequencing project supported by Ministry of
-CC   Economy, Trade and Industry of Japan; cDNA full insert sequencing:
-CC   Research Association for Biotechnology; cDNA library construction,
-CC   5'- & 3'-end one pass sequencing and clone selection: Helix
-CC   Research Institute (supported by Japan Key Technology Center etc.)
-CC   and Department of Virology, Institute of Medical Science,
-CC   University of Tokyo.
-XX
-FH   Key                 Location/Qualifiers
-FH
-FT   L-V-D-J-C-SEQUENCE  1..1605
-FT                       /clone="MAMMA1001080"
-FT                       /clone_lib="MAMMA1"
-FT                       /db_xref="taxon:9606"
-FT                       /organism="Homo sapiens"
-FT                       /productive
-FT                       /sequenced_mol="cDNA to mRNA"
-FT                       /tissue_type="mammary gland"
-FT   L-V-D-J-C-REGION    77..1558
-FT                       /translation="MELGLRWVFLVAFLEGVQCEVQLVESGGGLVKPGGSLRLSC
-FT                       AASGLSFSTYAMNWVRQAPGKGLEWVSSISSRSDYIYYRDSVKGRFTISRDNAKN
-FT                       SLYLQMNSLRVDDTAVYYCARDSCNGAICYGFSPWGQGTLVTVSSASPTSPKVFP
-FT                       LSLCSTQPDGNVVIACLVQGFFPQEPLSVTWSESGQGVTARNFPPSQDASGDLYT
-FT                       TSSQLTLPATQCLAGKSVTCHVKHYTNPSQDVTVPCPVPSTPPTPSPSTPPTPSP
-FT                       SCCHPRLSLHRPALEDLLLGSEANLTCTLTGLRDASGVTFTWTPSSGKSAVQGPP
-FT                       ERDLCGCYSVSSVLPGCAEPWNHGKTFTCTAAYPESKTPLTATLSKSGNTFRPEV
-FT                       HLLPPPSEELALNELVTLTCLARGFSPKDVLVRWLQGSQELPREKYLTWASRQEP
-FT                       SQGTTTFAVTSILRVAAEDWKKGDTFSCMVGHEALPLAFTQKTIDRLAGKPTHVN
-FT                       VSVVMAEVDGTCY"
-FT                       /protein_id="BAB55072.1"
-FT   5'UTR               1..76
-FT   L-V-D-J-REGION      77..499
-FT                       /translation="MELGLRWVFLVAFLEGVQCEVQLVESGGGLVKPGGSLRLSC
-FT                       AASGLSFSTYAMNWVRQAPGKGLEWVSSISSRSDYIYYRDSVKGRFTISRDNAKN
-FT                       SLYLQMNSLRVDDTAVYYCARDSCNGAICYGFSPWGQGTLVTVSS"
-FT   L-V-D-REGION        77..454
-FT                       /translation="MELGLRWVFLVAFLEGVQCEVQLVESGGGLVKPGGSLRLSC
-FT                       AASGLSFSTYAMNWVRQAPGKGLEWVSSISSRSDYIYYRDSVKGRFTISRDNAKN
-FT                       SLYLQMNSLRVDDTAVYYCARDSCNGAICY"
-FT   L-V-REGION          77..429
-FT                       /translation="MELGLRWVFLVAFLEGVQCEVQLVESGGGLVKPGGSLRLSC
-FT                       AASGLSFSTYAMNWVRQAPGKGLEWVSSISSRSDYIYYRDSVKGRFTISRDNAKN
-FT                       SLYLQMNSLRVDDTAVYYCAR"
-FT   L-REGION            77..133
-FT                       /translation="MELGLRWVFLVAFLEGVQC"
-FT   V-D-J-C-REGION      134..1558
-FT                       /translation="EVQLVESGGGLVKPGGSLRLSCAASGLSFSTYAMNWVRQAP
-FT                       GKGLEWVSSISSRSDYIYYRDSVKGRFTISRDNAKNSLYLQMNSLRVDDTAVYYC
-FT                       ARDSCNGAICYGFSPWGQGTLVTVSSASPTSPKVFPLSLCSTQPDGNVVIACLVQ
-FT                       GFFPQEPLSVTWSESGQGVTARNFPPSQDASGDLYTTSSQLTLPATQCLAGKSVT
-FT                       CHVKHYTNPSQDVTVPCPVPSTPPTPSPSTPPTPSPSCCHPRLSLHRPALEDLLL
-FT                       GSEANLTCTLTGLRDASGVTFTWTPSSGKSAVQGPPERDLCGCYSVSSVLPGCAE
-FT                       PWNHGKTFTCTAAYPESKTPLTATLSKSGNTFRPEVHLLPPPSEELALNELVTLT
-FT                       CLARGFSPKDVLVRWLQGSQELPREKYLTWASRQEPSQGTTTFAVTSILRVAAED
-FT                       WKKGDTFSCMVGHEALPLAFTQKTIDRLAGKPTHVNVSVVMAEVDGTCY"
-FT   INIT-CODON          77..79
-FT   V-D-J-REGION        134..499
-FT                       /translation="EVQLVESGGGLVKPGGSLRLSCAASGLSFSTYAMNWVRQAP
-FT                       GKGLEWVSSISSRSDYIYYRDSVKGRFTISRDNAKNSLYLQMNSLRVDDTAVYYC
-FT                       ARDSCNGAICYGFSPWGQGTLVTVSS"
-FT                       /CDR_length="[8.8.15]"
-FT                       /FR_length="[25.17.38.11]"
-FT   V-REGION            134..429
-FT                       /translation="EVQLVESGGGLVKPGGSLRLSCAASGLSFSTYAMNWVRQAP
-FT                       GKGLEWVSSISSRSDYIYYRDSVKGRFTISRDNAKNSLYLQMNSLRVDDTAVYYC
-FT                       AR"
-FT                       /IMGT_allele="IGHV3-21*02"
-FT                       /IMGT_gene="IGHV3-21"
-FT                       /Videntity="92,91% (275/296 nt)"
-FT   FR1-IMGT            134..208
-FT                       /translation="EVQLVESGGGLVKPGGSLRLSCAAS"
-FT                       /AA_IMGT="AA 1 to 26, AA 10 is missing"
-FT   1st-CYS             197..199
-FT   CDR1-IMGT           209..232
-FT                       /translation="GLSFSTYA"
-FT                       /AA_IMGT="AA 27 to 38, AA 31, 32, 33 and 34 are 
-FT                       missing"
-FT   FR2-IMGT            233..283
-FT                       /translation="MNWVRQAPGKGLEWVSS"
-FT                       /AA_IMGT="AA 39 to 55"
-FT   CONSERVED-TRP       239..241
-FT   CDR2-IMGT           284..307
-FT                       /translation="ISSRSDYI"
-FT                       /AA_IMGT="AA 56 to 65, AA 60 and 61 are missing"
-FT   FR3-IMGT            308..421
-FT                       /translation="YYRDSVKGRFTISRDNAKNSLYLQMNSLRVDDTAVYYC"
-FT                       /AA_IMGT="AA 66 to 104, AA 73 is missing"
-FT   2nd-CYS             419..421
-FT   CDR3-IMGT           422..466
-FT                       /translation="ARDSCNGAICYGFSP"
-FT                       /AA_IMGT="AA 105 to 117, AA 112.1 and 111.1 are added"
-FT   JUNCTION            419..469
-FT                       /translation="CARDSCNGAICYGFSPW"
-FT                       /in_frame
-FT   3'V-REGION          419..429
-FT                       /translation="CAR"
-FT   (N-D)-REGION        430..463
-FT                       /codon_start=2
-FT                       /translation="SCNGAICYGFS"
-FT   P-REGION            430
-FT   N1-REGION           431..432
-FT   D-J-REGION          433..499
-FT                       /codon_start=2
-FT                       /translation="CNGAICYGFSPWGQGTLVTVSS"
-FT   D-REGION            433..454
-FT                       /codon_start=2
-FT                       /translation="CNGAICY"
-FT                       /IMGT_allele="IGHD2-8*02"
-FT                       /IMGT_gene="IGHD2-8"
-FT   N2-REGION           455..463
-FT                       /translation="GFS"
-FT   5'J-REGION          464..469
-FT                       /translation="PW"
-FT   J-REGION            464..499
-FT                       /translation="PWGQGTLVTVSS"
-FT                       /IMGT_allele="IGHJ5*02"
-FT                       /IMGT_gene="IGHJ5"
-FT   J-TRP               467..469
-FT   FR4-IMGT            467..499
-FT                       /translation="WGQGTLVTVSS"
-FT                       /AA_IMGT="AA 118 to 128"
-FT   C-REGION            500..1558
-FT                       /translation="ASPTSPKVFPLSLCSTQPDGNVVIACLVQGFFPQEPLSVTW
-FT                       SESGQGVTARNFPPSQDASGDLYTTSSQLTLPATQCLAGKSVTCHVKHYTNPSQD
-FT                       VTVPCPVPSTPPTPSPSTPPTPSPSCCHPRLSLHRPALEDLLLGSEANLTCTLTG
-FT                       LRDASGVTFTWTPSSGKSAVQGPPERDLCGCYSVSSVLPGCAEPWNHGKTFTCTA
-FT                       AYPESKTPLTATLSKSGNTFRPEVHLLPPPSEELALNELVTLTCLARGFSPKDVL
-FT                       VRWLQGSQELPREKYLTWASRQEPSQGTTTFAVTSILRVAAEDWKKGDTFSCMVG
-FT                       HEALPLAFTQKTIDRLAGKPTHVNVSVVMAEVDGTCY"
-FT                       /IMGT_allele="IGHA1*01"
-FT                       /IMGT_gene="IGHA1"
-FT   STOP-CODON          1559..1561
-FT   3'UTR               1559..1605
-XX
-SQ   Sequence 1605 BP; 325 A; 525 C; 444 G; 311 T; 0 other;
-     tctgagagag gagccttagc cctggattcc aaggcctatc cacttggtga tcagcactga        60
-     gcaccgagga ttcaccatgg aactggggct ccgctgggtt ttccttgttg cttttttaga       120
-     aggtgtccag tgtgaggtgc aactggtgga gtctggggga ggcctggtca agccgggggg       180
-     gtccctgaga ctctcctgtg cagcctctgg attaagcttc agtacctatg ccatgaactg       240
-     ggtccgccag gctccaggga aggggctgga atgggtctca agtattagta gtagaagtga       300
-     ttacatatac tatagagact cagtgaaggg ccgattcacc atctccagag acaacgccaa       360
-     gaattcactg tatctgcaaa tgaatagcct gagagtcgac gacacggctg tctattactg       420
-     tgcgagagat tcttgtaatg gtgctatatg ttatggtttc agtccctggg gccagggaac       480
-     cctggtcacc gtctcctcag catccccgac cagccccaag gtcttcccgc tgagcctctg       540
-     cagcacccag ccagatggga acgtggtcat cgcctgcctg gtccagggct tcttccccca       600
-     ggagccactc agtgtgacct ggagcgaaag cggacagggc gtgaccgcca gaaacttccc       660
-     acccagccag gatgcctccg gggacctgta caccacgagc agccagctga ccctgccggc       720
-     cacacagtgc ctagccggca agtccgtgac atgccacgtg aagcactaca cgaatcccag       780
-     ccaggatgtg actgtgccct gcccagttcc ctcaactcca cctaccccat ctccctcaac       840
-     tccacctacc ccatctccct catgctgcca cccccgactg tcactgcacc gaccggccct       900
-     cgaggacctg ctcttaggtt cagaagcgaa cctcacgtgc acactgaccg gcctgagaga       960
-     tgcctcgggt gtcaccttca cctggacgcc ctcaagtggg aagagcgctg ttcaaggacc      1020
-     acctgagcgt gacctctgtg gctgctacag cgtgtccagt gtcctgccgg gctgtgccga      1080
-     gccatggaac catgggaaga ccttcacttg cactgctgcc taccccgagt ccaagacccc      1140
-     gctaaccgcc accctctcaa aatccggaaa cacattccgg cccgaggtcc acctgctgcc      1200
-     gccgccgtcg gaggagctgg ccctgaacga gctggtgacg ctgacgtgcc tggcacgtgg      1260
-     cttcagcccc aaggacgtgc tggttcgctg gctgcagggg tcacaggagc tgccccgcga      1320
-     gaagtacctg acttgggcat cccggcagga gcccagccag ggcaccacca ccttcgctgt      1380
-     gaccagcata ctgcgcgtgg cagccgagga ctggaagaag ggggacacct tctcctgcat      1440
-     ggtgggccac gaggccctgc cgctggcctt cacacagaag accatcgacc gcttggcggg      1500
-     taaacccacc catgtcaatg tgtctgttgt catggcggag gtggacggca cctgctactg      1560
-     agccgcccgc ctgtccccac ccctgaataa actccatgct ccccc                      1605
-//
-ID   AK093721; SV 1; linear; cDNA; STD; HUM; 1621 BP.
-XX
-AC   AK093721;
-XX
-DT   17-JUN-2003 (Rel. 200325-2, arrived in LIGM-DB)
-DT   15-JUN-2024 (Rel. 202424-6, Last updated, Version 6)
-XX
-DE   Homo sapiens cDNA FLJ36402 fis, clone THYMU2009906, highly similar to IG
-DE   ALPHA-1 CHAIN C REGION.
-XX
-KW   antigen receptor; Immunoglobulin superfamily (IgSF); immunoglobulin (IG);
-KW   IG-Heavy; IG-Heavy-Alpha; constant; IG-Heavy-Alpha-1-IGHA1; variable;
-KW   diversity; joining; regular; cDNA; undefined; rearranged; productive;
-KW   L-V-D-J-C-sequence.
-XX
-OS   Homo sapiens (human)
-OC   cellular organisms; Eukaryota; Opisthokonta; Metazoa; Eumetazoa; Bilateria;
-OC   Deuterostomia; Chordata; Craniata; Vertebrata; Gnathostomata; Teleostomi;
-OC   Euteleostomi; Sarcopterygii; Dipnotetrapodomorpha; Tetrapoda; Amniota;
-OC   Mammalia; Theria; Eutheria; Boreoeutheria; Euarchontoglires; Primates;
-OC   Haplorrhini; Simiiformes; Catarrhini; Hominoidea; Hominidae; Homininae;
-OC   Homo; Homo sapiens.
-XX
-RN   [1]
-RP   1-1621
-RX   DOI; 10.1007/s002510050692.
-RX   PUBMED; 10541813.
-RA   Miska K.B., Miller R.D.;
-RT   "Marsupial Mhc class I: classical sequences from the opossum, Monodelphis
-RT   domestica";
-RL   Immunogenetics 50(1-2):89-93(1999).
-XX
-RN   [2]
-RX   DOI; 10.1016/S0165-2478(97)00101-6.
-RX   PUBMED; 9373213.
-RA   Fukuoka M., Tokushima M., Koarada S., Sai T., Miyake K., Kimoto M.;
-RT   "Analysis of Vbeta4 T cell receptor CDR3 repertoire in BALB/c and (NZB x
-RT   NZW)F1 mice";
-RL   Immunol. Lett. 59(2):63-69(1997).
-XX
-RN   [3]
-RX   PUBMED; 8645581.
-RA   Okamoto S., Yoshikawa K., Obata Y., Shibuya M., Aoki S., Yoshida J.,
-RA   Takahashi T.;
-RT   "Monoclonal antibody against the fusion junction of a deletion-mutant
-RT   epidermal growth factor receptor";
-RL   Br. J. Cancer 73(11):1366-1372(1996).
-XX
-DR   H-InvDB; HIT000018588.19.
-DR   MD5; 90a9a9328b8aac418094f94c4f76433d.
-XX
-CC   IMGT/LIGM-DB annotation level: automatic
-CC
-CC   NEDO human cDNA sequencing project supported by Ministry of
-CC   Economy, Trade and Industry of Japan; cDNA full insert sequencing:
-CC   Research Association for Biotechnology (RAB); cDNA library
-CC   construction: Helix Research Institute (HRI) (supported by Japan
-CC   Key Technology Center etc.); 5'- & 3'-end one pass sequencing:
-CC   RAB, HRI, and Biotechnology Center, National Institute of
-CC   Technology and Evaluation; clone selection for full insert
-CC   sequencing: HRI and RAB; annotation: HRI and RAB.
-XX
-FH   Key                 Location/Qualifiers
-FH
-FT   L-V-D-J-C-SEQUENCE  1..1621
-FT                       /clone="THYMU2009906"
-FT                       /clone_lib="THYMU2"
-FT                       /db_xref="taxon:9606"
-FT                       /organism="Homo sapiens"
-FT                       /productive
-FT                       /sequenced_mol="cDNA to mRNA"
-FT                       /tissue_type="shymus"
-FT   L-V-D-J-C-REGION    80..1570
-FT                       /translation="MEFGLNWVVLAALLRGVQCQVQLVESGGGVVQPGTSLRLSC
-FT                       VVSGFTFTNFPMHWLRQAPGKGLEWVAVFSSDANDEFYVDSVKGRFTISRDIFSN
-FT                       TLYLHMTNLRPEDTAIYFCAREAYFDTSGDYSRAFDFWGQGTLVTVSSASPTSPK
-FT                       VFPLSLCSTQPDGNVVIACLVQGFFPQEPLSVTWSESGQGVTARNFPPSQDASGD
-FT                       LYTTSSQLTLPATQCLAGKSVTCHVKHYTNPSQDVTVPCPVPSTPPTPSPSTPPT
-FT                       PSPSCCHPRLSLHRPALEDLLLGSEANLTCTLTGLRDASGVTFTWTPSSGKSAVQ
-FT                       GPPDRDLCGCYSVSSVLPGCAEPWNHGKTFTCTAAYPESKTPLTATLSKSGNTFR
-FT                       PEVHLLPPPSEELALNELVTLTCLARGFSPKDVLVRWLQGSQELPREKYLTWASR
-FT                       QEPSQGTTTFAVTSILRVAAEDWKKGDTFSCMVGHEALPLAFTQKTIDRLAGKPT
-FT                       HVNVSVVMAEVDGTCY"
-FT   5'UTR               1..79
-FT   L-V-D-J-REGION      80..511
-FT                       /translation="MEFGLNWVVLAALLRGVQCQVQLVESGGGVVQPGTSLRLSC
-FT                       VVSGFTFTNFPMHWLRQAPGKGLEWVAVFSSDANDEFYVDSVKGRFTISRDIFSN
-FT                       TLYLHMTNLRPEDTAIYFCAREAYFDTSGDYSRAFDFWGQGTLVTVSS"
-FT   L-V-D-REGION        80..461
-FT                       /translation="MEFGLNWVVLAALLRGVQCQVQLVESGGGVVQPGTSLRLSC
-FT                       VVSGFTFTNFPMHWLRQAPGKGLEWVAVFSSDANDEFYVDSVKGRFTISRDIFSN
-FT                       TLYLHMTNLRPEDTAIYFCAREAYFDTSGDY"
-FT   L-V-REGION          80..429
-FT                       /translation="MEFGLNWVVLAALLRGVQCQVQLVESGGGVVQPGTSLRLSC
-FT                       VVSGFTFTNFPMHWLRQAPGKGLEWVAVFSSDANDEFYVDSVKGRFTISRDIFSN
-FT                       TLYLHMTNLRPEDTAIYFCA"
-FT   L-REGION            80..136
-FT                       /translation="MEFGLNWVVLAALLRGVQC"
-FT   V-D-J-C-REGION      137..1570
-FT                       /translation="QVQLVESGGGVVQPGTSLRLSCVVSGFTFTNFPMHWLRQAP
-FT                       GKGLEWVAVFSSDANDEFYVDSVKGRFTISRDIFSNTLYLHMTNLRPEDTAIYFC
-FT                       AREAYFDTSGDYSRAFDFWGQGTLVTVSSASPTSPKVFPLSLCSTQPDGNVVIAC
-FT                       LVQGFFPQEPLSVTWSESGQGVTARNFPPSQDASGDLYTTSSQLTLPATQCLAGK
-FT                       SVTCHVKHYTNPSQDVTVPCPVPSTPPTPSPSTPPTPSPSCCHPRLSLHRPALED
-FT                       LLLGSEANLTCTLTGLRDASGVTFTWTPSSGKSAVQGPPDRDLCGCYSVSSVLPG
-FT                       CAEPWNHGKTFTCTAAYPESKTPLTATLSKSGNTFRPEVHLLPPPSEELALNELV
-FT                       TLTCLARGFSPKDVLVRWLQGSQELPREKYLTWASRQEPSQGTTTFAVTSILRVA
-FT                       AEDWKKGDTFSCMVGHEALPLAFTQKTIDRLAGKPTHVNVSVVMAEVDGTCY"
-FT   INIT-CODON          80..82
-FT   V-D-J-REGION        137..511
-FT                       /translation="QVQLVESGGGVVQPGTSLRLSCVVSGFTFTNFPMHWLRQAP
-FT                       GKGLEWVAVFSSDANDEFYVDSVKGRFTISRDIFSNTLYLHMTNLRPEDTAIYFC
-FT                       AREAYFDTSGDYSRAFDFWGQGTLVTVSS"
-FT                       /CDR_length="[8.8.18]"
-FT                       /FR_length="[25.17.38.11]"
-FT   V-REGION            137..429
-FT                       /translation="QVQLVESGGGVVQPGTSLRLSCVVSGFTFTNFPMHWLRQAP
-FT                       GKGLEWVAVFSSDANDEFYVDSVKGRFTISRDIFSNTLYLHMTNLRPEDTAIYFC
-FT                       A"
-FT                       /IMGT_allele="IGHV3-30-3*01"
-FT                       /IMGT_gene="IGHV3-30-3"
-FT                       /Videntity="85,67% (251/293 nt)"
-FT   FR1-IMGT            137..211
-FT                       /translation="QVQLVESGGGVVQPGTSLRLSCVVS"
-FT                       /AA_IMGT="AA 1 to 26, AA 10 is missing"
-FT   1st-CYS             200..202
-FT   CDR1-IMGT           212..235
-FT                       /translation="GFTFTNFP"
-FT                       /AA_IMGT="AA 27 to 38, AA 31, 32, 33 and 34 are 
-FT                       missing"
-FT   FR2-IMGT            236..286
-FT                       /translation="MHWLRQAPGKGLEWVAV"
-FT                       /AA_IMGT="AA 39 to 55"
-FT   CONSERVED-TRP       242..244
-FT   CDR2-IMGT           287..310
-FT                       /translation="FSSDANDE"
-FT                       /AA_IMGT="AA 56 to 65, AA 60 and 61 are missing"
-FT   FR3-IMGT            311..424
-FT                       /translation="FYVDSVKGRFTISRDIFSNTLYLHMTNLRPEDTAIYFC"
-FT                       /AA_IMGT="AA 66 to 104, AA 73 is missing"
-FT   2nd-CYS             422..424
-FT   CDR3-IMGT           425..478
-FT                       /translation="AREAYFDTSGDYSRAFDF"
-FT                       /AA_IMGT="AA 105 to 117, AA 112.1, 111.1, 112.2, 111.2 
-FT                       and 112.3 are added"
-FT   JUNCTION            422..481
-FT                       /translation="CAREAYFDTSGDYSRAFDFW"
-FT                       /in_frame
-FT   3'V-REGION          422..429
-FT                       /translation="CA"
-FT   (N-D)-REGION        430..469
-FT                       /codon_start=2
-FT                       /translation="EAYFDTSGDYSRA"
-FT   N1-REGION           430..436
-FT                       /codon_start=2
-FT                       /translation="EA"
-FT   D-J-REGION          437..511
-FT                       /translation="YFDTSGDYSRAFDFWGQGTLVTVSS"
-FT   D-REGION            437..461
-FT                       /translation="YFDTSGDY"
-FT                       /IMGT_allele="IGHD3-22*01"
-FT                       /IMGT_gene="IGHD3-22"
-FT   N2-REGION           462..469
-FT                       /codon_start=3
-FT                       /translation="RA"
-FT   5'J-REGION          470..481
-FT                       /translation="FDFW"
-FT   J-REGION            470..511
-FT                       /translation="FDFWGQGTLVTVSS"
-FT                       /IMGT_allele="IGHJ4*02"
-FT                       /IMGT_gene="IGHJ4"
-FT   J-TRP               479..481
-FT   FR4-IMGT            479..511
-FT                       /translation="WGQGTLVTVSS"
-FT                       /AA_IMGT="AA 118 to 128"
-FT   C-REGION            512..1570
-FT                       /translation="ASPTSPKVFPLSLCSTQPDGNVVIACLVQGFFPQEPLSVTW
-FT                       SESGQGVTARNFPPSQDASGDLYTTSSQLTLPATQCLAGKSVTCHVKHYTNPSQD
-FT                       VTVPCPVPSTPPTPSPSTPPTPSPSCCHPRLSLHRPALEDLLLGSEANLTCTLTG
-FT                       LRDASGVTFTWTPSSGKSAVQGPPDRDLCGCYSVSSVLPGCAEPWNHGKTFTCTA
-FT                       AYPESKTPLTATLSKSGNTFRPEVHLLPPPSEELALNELVTLTCLARGFSPKDVL
-FT                       VRWLQGSQELPREKYLTWASRQEPSQGTTTFAVTSILRVAAEDWKKGDTFSCMVG
-FT                       HEALPLAFTQKTIDRLAGKPTHVNVSVVMAEVDGTCY"
-FT                       /IMGT_allele="IGHA1*01"
-FT                       /IMGT_gene="IGHA1"
-FT   STOP-CODON          1571..1573
-FT   3'UTR               1571..1621
-XX
-SQ   Sequence 1621 BP; 324 A; 542 C; 436 G; 319 T; 0 other;
-     aactctggga gacgagccca gcacaggaag tcgccggcgt ttccattcgg tgatcaccac        60
-     tgaacacaga ggactcacca tggagtttgg gctgaactgg gttgtcctcg ctgctctttt       120
-     aagaggtgtc cagtgtcagg tgcaattggt ggaatctggg ggaggcgtgg tccagcctgg       180
-     gacgtccttg agactctcct gtgtagtctc tggattcacc ttcactaatt ttcctatgca       240
-     ctggctccgc caggctccag gcaagggact ggagtgggtg gcagttttct catctgatgc       300
-     gaacgatgaa ttctatgtag actccgtgaa gggccgattc accatctcca gagacatttt       360
-     cagcaatacc ctatatttac acatgaccaa cctgcgacct gaggacacgg ctatctattt       420
-     ctgtgcgagg gaggcatact ttgatactag tggtgactac tccagagctt ttgacttctg       480
-     gggccaggga accctcgtca ccgtgtcctc agcatccccg accagcccca aggtcttccc       540
-     gctgagcctc tgcagcaccc agccagatgg gaacgtggtc atcgcctgcc tggtccaggg       600
-     cttcttcccc caggagccac tcagtgtgac ctggagcgaa agcggacagg gcgtgaccgc       660
-     cagaaacttc ccacccagcc aggatgcctc cggggacctg tacaccacga gcagccagct       720
-     gaccctgccg gccacacagt gcctagccgg caagtccgtg acatgccacg tgaagcacta       780
-     cacgaatccc agccaggatg tgactgtgcc ctgcccagtt ccctcaactc cacctacccc       840
-     atctccctca actccaccta ccccatctcc ctcatgctgc cacccccgac tgtctctgca       900
-     ccgaccggcc ctcgaggacc tgctcttagg ttcagaagcg aacctcacgt gcacactgac       960
-     cggcctgaga gatgcctcag gtgtcacctt cacctggacg ccctcaagtg ggaagagcgc      1020
-     tgttcaagga ccacctgacc gtgacctctg tggctgctac agcgtgtcca gtgtcctgcc      1080
-     gggctgtgcc gagccatgga accatgggaa gaccttcact tgcactgctg cctaccccga      1140
-     gtccaagacc ccgctaaccg ccaccctctc aaaatccgga aacacattcc ggcccgaggt      1200
-     ccacctgctg ccgccgccgt cggaggagct ggccctgaac gagctggtga cgctgacgtg      1260
-     cctggcacgt ggcttcagcc ccaaggatgt gctggttcgc tggctgcagg ggtcacagga      1320
-     gctgccccgc gagaagtacc tgacttgggc atcccggcag gagcccagcc agggcaccac      1380
-     caccttcgct gtgaccagca tactgcgcgt ggcagccgag gactggaaga agggggacac      1440
-     cttctcctgc atggtgggcc acgaggccct gccgctggcc ttcacacaga agaccatcga      1500
-     ccgcttggcg ggtaaaccca cccatgtcaa tgtgtctgtt gtcatggcgg aggtggacgg      1560
-     cacctgctac tgagccgccc gcctgtcccc acccctgaat aaactccatg ctcccccaag      1620
-     c                                                                      1621
-//
-ID   AK128476; SV 1; linear; cDNA; STD; HUM; 1602 BP.
-XX
-AC   AK128476;
-XX
-DT   30-SEP-2003 (Rel. 200340-2, arrived in LIGM-DB)
-DT   15-JUN-2024 (Rel. 202424-6, Last updated, Version 10)
-XX
-DE   Homo sapiens cDNA FLJ46621 fis, clone TLUNG2001445, highly similar to Ig
-DE   alpha-1 chain C region.
-XX
-KW   antigen receptor; Immunoglobulin superfamily (IgSF); immunoglobulin (IG);
-KW   IG-Heavy; IG-Heavy-Alpha; constant; IG-Heavy-Alpha-1-IGHA1; variable;
-KW   diversity; joining; regular; cDNA; undefined; rearranged; productive;
-KW   L-V-D-J-C-sequence.
-XX
-OS   Homo sapiens (human)
-OC   cellular organisms; Eukaryota; Opisthokonta; Metazoa; Eumetazoa; Bilateria;
-OC   Deuterostomia; Chordata; Craniata; Vertebrata; Gnathostomata; Teleostomi;
-OC   Euteleostomi; Sarcopterygii; Dipnotetrapodomorpha; Tetrapoda; Amniota;
-OC   Mammalia; Theria; Eutheria; Boreoeutheria; Euarchontoglires; Primates;
-OC   Haplorrhini; Simiiformes; Catarrhini; Hominoidea; Hominidae; Homininae;
-OC   Homo; Homo sapiens.
-XX
-RN   [1]
-RP   1-1602
-RA   Timmusk S.;
-RT   ;
-RL   Submitted (23-NOV-1999) to the INSDC.
-RL   Timmusk S., BMC, Immunology Programme, Dept. of Cell and Molecular Biology,
-RL   P.O.box 596, Husargatan 3, S-751 24 Uppsala, SWEDEN.
-XX
-RN   [2]
-RX   DOI; 10.1016/S0165-2478(97)00101-6.
-RX   PUBMED; 9373213.
-RA   Fukuoka M., Tokushima M., Koarada S., Sai T., Miyake K., Kimoto M.;
-RT   "Analysis of Vbeta4 T cell receptor CDR3 repertoire in BALB/c and (NZB x
-RT   NZW)F1 mice";
-RL   Immunol. Lett. 59(2):63-69(1997).
-XX
-DR   MD5; 5b97194caaece55c9edc9a7aca496def.
-XX
-CC   IMGT/LIGM-DB annotation level: automatic
-CC
-CC   NEDO human cDNA sequencing project supported by Ministry of
-CC   Economy, Trade and Industry of Japan; cDNA full insert sequencing:
-CC   Research Association for Biotechnology (RAB); cDNA library
-CC   construction: Helix Research Institute (HRI) (supported by Japan
-CC   Key Technology Center etc.); 5'- & 3'-end one pass sequencing:
-CC   RAB, HRI, and Biotechnology Center, National Institute of
-CC   Technology and Evaluation; clone selection for full insert
-CC   sequencing: HRI and RAB; annotation: Reverse Proteomics Research
-CC   Institute, HRI and RAB.
-XX
-FH   Key                 Location/Qualifiers
-FH
-FT   L-V-D-J-C-SEQUENCE  1..1602
-FT                       /clone="TLUNG2001445"
-FT                       /clone_lib="TLUNG2"
-FT                       /db_xref="taxon:9606"
-FT                       /organism="Homo sapiens"
-FT                       /productive
-FT                       /tissue_type="lung, tumor tissue"
-FT   L-V-D-J-C-REGION    80..1555
-FT                       /translation="MELGLSWVFLVAILKGVQCEVQLVESGGGLVQPGGSRRLSC
-FT                       AASAFTVSNNYVSWVRQAPGKGLEWVSIIYSAGDTYYADSVKGRFTISRDNSKNT
-FT                       LHLQMNSLRADDTAIYYCARMGGGFLGNAFEIWGQGTLMTVSSASPTSPKVFPLS
-FT                       LCSTQPDGNVVIACLVQGFFPQEPLSVTWSESGQGVTARNFPPSQDASGDLYTTS
-FT                       SQLTLPATQCLAGKSVTCHVKHYTNPSQDVTVPCPVPSTPPTPSPSTPPTPSPSC
-FT                       CHPRLSLHRPALEDLLLGSEANLTCTLTGLRDASGVTFTWTPSSGKSAVQGPPER
-FT                       DLCGCYSVSSVLPGCAEPWNHGKTFTCTAAYPESKTPLTATLSKSGNTFRPEVHL
-FT                       LPPPSEELALNELVTLTCLARGFSPKDVLVRWLQGSQELPREKYLTWASRQEPSQ
-FT                       GTTTFAVTSILRVAAEDWKKGDTFSCMVGHEALPLAFTQKTIDRLAGKPTHVNVS
-FT                       VVMAEVDGTCY"
-FT                       /protein_id="BAC87456.1"
-FT   5'UTR               1..79
-FT   L-V-D-J-REGION      80..496
-FT                       /translation="MELGLSWVFLVAILKGVQCEVQLVESGGGLVQPGGSRRLSC
-FT                       AASAFTVSNNYVSWVRQAPGKGLEWVSIIYSAGDTYYADSVKGRFTISRDNSKNT
-FT                       LHLQMNSLRADDTAIYYCARMGGGFLGNAFEIWGQGTLMTVSS"
-FT   L-V-D-REGION        80..444
-FT                       /translation="MELGLSWVFLVAILKGVQCEVQLVESGGGLVQPGGSRRLSC
-FT                       AASAFTVSNNYVSWVRQAPGKGLEWVSIIYSAGDTYYADSVKGRFTISRDNSKNT
-FT                       LHLQMNSLRADDTAIYYCARMGGGF"
-FT   L-V-REGION          80..427
-FT                       /translation="MELGLSWVFLVAILKGVQCEVQLVESGGGLVQPGGSRRLSC
-FT                       AASAFTVSNNYVSWVRQAPGKGLEWVSIIYSAGDTYYADSVKGRFTISRDNSKNT
-FT                       LHLQMNSLRADDTAIYYCAR"
-FT   L-REGION            80..136
-FT                       /translation="MELGLSWVFLVAILKGVQC"
-FT   V-D-J-C-REGION      137..1555
-FT                       /translation="EVQLVESGGGLVQPGGSRRLSCAASAFTVSNNYVSWVRQAP
-FT                       GKGLEWVSIIYSAGDTYYADSVKGRFTISRDNSKNTLHLQMNSLRADDTAIYYCA
-FT                       RMGGGFLGNAFEIWGQGTLMTVSSASPTSPKVFPLSLCSTQPDGNVVIACLVQGF
-FT                       FPQEPLSVTWSESGQGVTARNFPPSQDASGDLYTTSSQLTLPATQCLAGKSVTCH
-FT                       VKHYTNPSQDVTVPCPVPSTPPTPSPSTPPTPSPSCCHPRLSLHRPALEDLLLGS
-FT                       EANLTCTLTGLRDASGVTFTWTPSSGKSAVQGPPERDLCGCYSVSSVLPGCAEPW
-FT                       NHGKTFTCTAAYPESKTPLTATLSKSGNTFRPEVHLLPPPSEELALNELVTLTCL
-FT                       ARGFSPKDVLVRWLQGSQELPREKYLTWASRQEPSQGTTTFAVTSILRVAAEDWK
-FT                       KGDTFSCMVGHEALPLAFTQKTIDRLAGKPTHVNVSVVMAEVDGTCY"
-FT   INIT-CODON          80..82
-FT   V-D-J-REGION        137..496
-FT                       /translation="EVQLVESGGGLVQPGGSRRLSCAASAFTVSNNYVSWVRQAP
-FT                       GKGLEWVSIIYSAGDTYYADSVKGRFTISRDNSKNTLHLQMNSLRADDTAIYYCA
-FT                       RMGGGFLGNAFEIWGQGTLMTVSS"
-FT                       /CDR_length="[8.7.14]"
-FT                       /FR_length="[25.17.38.11]"
-FT   V-REGION            137..427
-FT                       /translation="EVQLVESGGGLVQPGGSRRLSCAASAFTVSNNYVSWVRQAP
-FT                       GKGLEWVSIIYSAGDTYYADSVKGRFTISRDNSKNTLHLQMNSLRADDTAIYYCA
-FT                       R"
-FT                       /IMGT_allele="IGHV3-66*01 or IGHV3-66*04"
-FT                       /IMGT_gene="IGHV3-66"
-FT                       /Videntity="93,47% (272/291 nt)"
-FT   FR1-IMGT            137..211
-FT                       /translation="EVQLVESGGGLVQPGGSRRLSCAAS"
-FT                       /AA_IMGT="AA 1 to 26, AA 10 is missing"
-FT   1st-CYS             200..202
-FT   CDR1-IMGT           212..235
-FT                       /translation="AFTVSNNY"
-FT                       /AA_IMGT="AA 27 to 38, AA 31, 32, 33 and 34 are 
-FT                       missing"
-FT   FR2-IMGT            236..286
-FT                       /translation="VSWVRQAPGKGLEWVSI"
-FT                       /AA_IMGT="AA 39 to 55"
-FT   CONSERVED-TRP       242..244
-FT   CDR2-IMGT           287..307
-FT                       /translation="IYSAGDT"
-FT                       /AA_IMGT="AA 56 to 65, AA 60, 61 and 62 are missing"
-FT   FR3-IMGT            308..421
-FT                       /translation="YYADSVKGRFTISRDNSKNTLHLQMNSLRADDTAIYYC"
-FT                       /AA_IMGT="AA 66 to 104, AA 73 is missing"
-FT   2nd-CYS             419..421
-FT   CDR3-IMGT           422..463
-FT                       /translation="ARMGGGFLGNAFEI"
-FT                       /AA_IMGT="AA 105 to 117, AA 112.1 is added"
-FT   JUNCTION            419..466
-FT                       /translation="CARMGGGFLGNAFEIW"
-FT                       /in_frame
-FT   3'V-REGION          419..427
-FT                       /translation="CAR"
-FT   (N-D)-J-REGION      428..496
-FT                       /translation="MGGGFLGNAFEIWGQGTLMTVSS"
-FT   (N-D)-REGION        428..449
-FT                       /translation="MGGGFLG"
-FT   N1-REGION           428..430
-FT   D-J-REGION          431..496
-FT                       /translation="GGGFLGNAFEIWGQGTLMTVSS"
-FT   D-REGION            431..444
-FT                       /translation="GGGF"
-FT                       /IMGT_allele="IGHD3-16*01"
-FT                       /IMGT_gene="IGHD3-16"
-FT   N2-REGION           445..449
-FT                       /codon_start=2
-FT                       /translation="G"
-FT   5'J-REGION          450..466
-FT                       /translation="MLLRS"
-FT   J-REGION            450..496
-FT                       /codon_start=3
-FT                       /translation="AFEIWGQGTLMTVSS"
-FT                       /IMGT_allele="IGHJ3*02"
-FT                       /IMGT_gene="IGHJ3"
-FT   J-TRP               464..466
-FT   FR4-IMGT            464..496
-FT                       /translation="WGQGTLMTVSS"
-FT                       /AA_IMGT="AA 118 to 128"
-FT   C-REGION            497..1555
-FT                       /translation="ASPTSPKVFPLSLCSTQPDGNVVIACLVQGFFPQEPLSVTW
-FT                       SESGQGVTARNFPPSQDASGDLYTTSSQLTLPATQCLAGKSVTCHVKHYTNPSQD
-FT                       VTVPCPVPSTPPTPSPSTPPTPSPSCCHPRLSLHRPALEDLLLGSEANLTCTLTG
-FT                       LRDASGVTFTWTPSSGKSAVQGPPERDLCGCYSVSSVLPGCAEPWNHGKTFTCTA
-FT                       AYPESKTPLTATLSKSGNTFRPEVHLLPPPSEELALNELVTLTCLARGFSPKDVL
-FT                       VRWLQGSQELPREKYLTWASRQEPSQGTTTFAVTSILRVAAEDWKKGDTFSCMVG
-FT                       HEALPLAFTQKTIDRLAGKPTHVNVSVVMAEVDGTCY"
-FT                       /IMGT_allele="IGHA1*01"
-FT                       /IMGT_gene="IGHA1"
-FT   STOP-CODON          1556..1558
-FT   3'UTR               1556..1602
-XX
-SQ   Sequence 1602 BP; 321 A; 529 C; 452 G; 300 T; 0 other;
-     agctctggga gaggagccca gcactgggat tccgaggtgt ttccattcag tgatctgcac        60
-     tgaacacaga ggactcgcca tggagttggg gctgagctgg gttttccttg ttgctatttt       120
-     aaaaggtgtc cagtgtgagg tgcagctggt ggagtcgggg ggaggcttgg tccagcccgg       180
-     ggggtcccgg agactctcct gtgcagcctc tgcattcacc gtcagcaaca attacgtgag       240
-     ctgggtccgc caggctccag ggaaggggct ggagtgggtc tcaatcattt atagcgctgg       300
-     tgacacatac tacgcagact ccgtgaaggg cagattcacc atctccagag acaactccaa       360
-     gaacactctg catcttcaaa tgaacagcct gagagccgac gacacggcta tttattactg       420
-     tgcgagaatg gggggtggtt tcctcgggaa tgcttttgag atctggggcc aagggacatt       480
-     gatgaccgtc tcttcagcat ccccgaccag ccccaaggtc ttcccgctga gcctctgcag       540
-     cacccagcca gatgggaacg tggtcatcgc ctgcctggtc cagggcttct tcccccagga       600
-     gccactcagt gtgacctgga gcgaaagcgg acagggcgtg accgccagaa acttcccacc       660
-     cagccaggat gcctccgggg acctgtacac cacgagcagc cagctgaccc tgccggccac       720
-     acagtgccta gccggcaagt ccgtgacatg ccacgtgaag cactacacga atcccagcca       780
-     ggatgtgact gtgccctgcc cagttccctc aactccacct accccatctc cctcaactcc       840
-     acctacccca tctccctcat gctgccaccc ccgactgtca ctgcaccgac cggccctcga       900
-     ggacctgctc ttaggttcag aagcgaacct cacgtgcaca ctgaccggcc tgagagatgc       960
-     ctcaggtgtc accttcacct ggacgccctc aagtgggaag agcgctgttc aaggaccacc      1020
-     tgagcgtgac ctctgtggct gctacagcgt gtccagtgtc ctgccgggct gtgccgagcc      1080
-     atggaaccat gggaagacct tcacttgcac tgctgcctac cccgagtcca agaccccgct      1140
-     aaccgccacc ctctcaaaat ccggaaacac attccggccc gaggtccacc tgctgccgcc      1200
-     gccgtcggag gagctggccc tgaacgagct ggtgacgctg acgtgcctgg cacgcggctt      1260
-     cagccccaag gacgtgctgg ttcgctggct gcaggggtca caggagctgc cccgcgagaa      1320
-     gtacctgact tgggcatccc ggcaggagcc cagccagggc accaccacct tcgctgtgac      1380
-     cagcatactg cgcgtggcag ccgaggactg gaagaagggg gacaccttct cctgcatggt      1440
-     gggccacgag gccctgccgc tggccttcac acagaagacc atcgaccgct tggcgggtaa      1500
-     acccacccat gtcaatgtgt ctgttgtcat ggcggaggtg gacggcacct gctactgagc      1560
-     cgcccgcctg tccccacccc tgaataaact ccatgctccc cc                         1602
-//
-ID   AK128565; SV 1; linear; cDNA; STD; HUM; 1603 BP.
-XX
-AC   AK128565;
-XX
-DT   30-SEP-2003 (Rel. 200340-2, arrived in LIGM-DB)
-DT   15-JUN-2024 (Rel. 202424-6, Last updated, Version 9)
-XX
-DE   Homo sapiens cDNA FLJ46724 fis, clone TRACH3018907, highly similar to Ig
-DE   alpha-1 chain C region.
-XX
-KW   antigen receptor; Immunoglobulin superfamily (IgSF); immunoglobulin (IG);
-KW   IG-Heavy; IG-Heavy-Alpha; constant; IG-Heavy-Alpha-1-IGHA1; variable;
-KW   diversity; joining; regular; cDNA; undefined; rearranged; productive;
-KW   L-V-D-J-C-sequence.
-XX
-OS   Homo sapiens (human)
-OC   cellular organisms; Eukaryota; Opisthokonta; Metazoa; Eumetazoa; Bilateria;
-OC   Deuterostomia; Chordata; Craniata; Vertebrata; Gnathostomata; Teleostomi;
-OC   Euteleostomi; Sarcopterygii; Dipnotetrapodomorpha; Tetrapoda; Amniota;
-OC   Mammalia; Theria; Eutheria; Boreoeutheria; Euarchontoglires; Primates;
-OC   Haplorrhini; Simiiformes; Catarrhini; Hominoidea; Hominidae; Homininae;
-OC   Homo; Homo sapiens.
-XX
-RN   [1]
-RP   1-1603
-RA   Isogai T., Yamamoto J.;
-RT   ;
-RL   Submitted (15-JUL-2003) to the INSDC.
-RL   Contact:Takao Isogai Helix Research Institute, Genomics Laboratory; 1532-3
-RL   Yana, Kisarazu, Chiba 292-0812, Japan E-mail :flj-cdna@nifty.com
-XX
-RN   [2]
-RX   DOI; 10.1016/S0165-2478(97)00101-6.
-RX   PUBMED; 9373213.
-RA   Fukuoka M., Tokushima M., Koarada S., Sai T., Miyake K., Kimoto M.;
-RT   "Analysis of Vbeta4 T cell receptor CDR3 repertoire in BALB/c and (NZB x
-RT   NZW)F1 mice";
-RL   Immunol. Lett. 59(2):63-69(1997).
-XX
-DR   MD5; 3c162efb9bdb8b0c8eaec90909a9a772.
-XX
-CC   IMGT/LIGM-DB annotation level: automatic
-CC
-CC   NEDO human cDNA sequencing project supported by Ministry of
-CC   Economy, Trade and Industry of Japan; cDNA full insert sequencing:
-CC   Research Association for Biotechnology (RAB); cDNA library
-CC   construction: Helix Research Institute (HRI) (supported by Japan
-CC   Key Technology Center etc.); 5'- & 3'-end one pass sequencing:
-CC   RAB, HRI, and Biotechnology Center, National Institute of
-CC   Technology and Evaluation; clone selection for full insert
-CC   sequencing: HRI and RAB; annotation: Reverse Proteomics Research
-CC   Institute, HRI and RAB.
-XX
-FH   Key                 Location/Qualifiers
-FH
-FT   L-V-D-J-C-SEQUENCE  1..1603
-FT                       /clone="TRACH3018907"
-FT                       /clone_lib="TRACH3"
-FT                       /db_xref="taxon:9606"
-FT                       /organism="Homo sapiens"
-FT                       /productive
-FT                       /tissue_type="trachea"
-FT   L-V-D-J-C-REGION    81..1556
-FT                       /translation="MELGLSWIFLLAILKGVQCEVQLVESGGGLVQPGRPLRLSC
-FT                       AASGFTFDYYAMHWVRQAPGKGLEWVSGITWNSGDMGYADSVKGRFTISRDIAKN
-FT                       SLYLQMNSLRAEDTALYYCAKDQQQLFDSFDIWGQGTMVTVSSASPTSPKVFPLS
-FT                       LCSTQPDGNVVIACLVQGFFPQEPLSVTWSESGQGVTARNFPPSQDASGDLYTTS
-FT                       SQLTLPATQCLAGKSVTCHVKHYTNPSQDVTVPCPVPSTPPTPSPSTPPTPSPSC
-FT                       CHPRLSLHRPALEDLLLGSEANLTCTLTGLRDASGVTFTWTPSSGKSAVQGPPDR
-FT                       DLCGCYSVSSVLPGCAEPWNHGKTFTCTAAYPESKTPLTATLSKSGNTFRPEVHL
-FT                       LPPPSEELALNELVTLTCLARGFSPKDVLVRWLQGSQELPREKYLTWASRQEPSQ
-FT                       GTTTFAVTSILRVAAEDWKKGDTFSCMVGHEALPLAFTQKTIDRLAGKPTHVNVS
-FT                       VVMAEVDGTCY"
-FT                       /protein_id="BAC87503.1"
-FT   5'UTR               1..80
-FT   L-V-D-J-REGION      81..497
-FT                       /translation="MELGLSWIFLLAILKGVQCEVQLVESGGGLVQPGRPLRLSC
-FT                       AASGFTFDYYAMHWVRQAPGKGLEWVSGITWNSGDMGYADSVKGRFTISRDIAKN
-FT                       SLYLQMNSLRAEDTALYYCAKDQQQLFDSFDIWGQGTMVTVSS"
-FT   L-V-D-REGION        81..445
-FT                       /translation="MELGLSWIFLLAILKGVQCEVQLVESGGGLVQPGRPLRLSC
-FT                       AASGFTFDYYAMHWVRQAPGKGLEWVSGITWNSGDMGYADSVKGRFTISRDIAKN
-FT                       SLYLQMNSLRAEDTALYYCAKDQQQ"
-FT   L-V-REGION          81..433
-FT                       /translation="MELGLSWIFLLAILKGVQCEVQLVESGGGLVQPGRPLRLSC
-FT                       AASGFTFDYYAMHWVRQAPGKGLEWVSGITWNSGDMGYADSVKGRFTISRDIAKN
-FT                       SLYLQMNSLRAEDTALYYCAK"
-FT   L-REGION            81..137
-FT                       /translation="MELGLSWIFLLAILKGVQC"
-FT   V-D-J-C-REGION      138..1556
-FT                       /translation="EVQLVESGGGLVQPGRPLRLSCAASGFTFDYYAMHWVRQAP
-FT                       GKGLEWVSGITWNSGDMGYADSVKGRFTISRDIAKNSLYLQMNSLRAEDTALYYC
-FT                       AKDQQQLFDSFDIWGQGTMVTVSSASPTSPKVFPLSLCSTQPDGNVVIACLVQGF
-FT                       FPQEPLSVTWSESGQGVTARNFPPSQDASGDLYTTSSQLTLPATQCLAGKSVTCH
-FT                       VKHYTNPSQDVTVPCPVPSTPPTPSPSTPPTPSPSCCHPRLSLHRPALEDLLLGS
-FT                       EANLTCTLTGLRDASGVTFTWTPSSGKSAVQGPPDRDLCGCYSVSSVLPGCAEPW
-FT                       NHGKTFTCTAAYPESKTPLTATLSKSGNTFRPEVHLLPPPSEELALNELVTLTCL
-FT                       ARGFSPKDVLVRWLQGSQELPREKYLTWASRQEPSQGTTTFAVTSILRVAAEDWK
-FT                       KGDTFSCMVGHEALPLAFTQKTIDRLAGKPTHVNVSVVMAEVDGTCY"
-FT   INIT-CODON          81..83
-FT   V-D-J-REGION        138..497
-FT                       /translation="EVQLVESGGGLVQPGRPLRLSCAASGFTFDYYAMHWVRQAP
-FT                       GKGLEWVSGITWNSGDMGYADSVKGRFTISRDIAKNSLYLQMNSLRAEDTALYYC
-FT                       AKDQQQLFDSFDIWGQGTMVTVSS"
-FT                       /CDR_length="[8.8.13]"
-FT                       /FR_length="[25.17.38.11]"
-FT   V-REGION            138..433
-FT                       /translation="EVQLVESGGGLVQPGRPLRLSCAASGFTFDYYAMHWVRQAP
-FT                       GKGLEWVSGITWNSGDMGYADSVKGRFTISRDIAKNSLYLQMNSLRAEDTALYYC
-FT                       AK"
-FT                       /IMGT_allele="IGHV3-9*01"
-FT                       /IMGT_gene="IGHV3-9"
-FT                       /Videntity="96,96% (287/296 nt)"
-FT   FR1-IMGT            138..212
-FT                       /translation="EVQLVESGGGLVQPGRPLRLSCAAS"
-FT                       /AA_IMGT="AA 1 to 26, AA 10 is missing"
-FT   1st-CYS             201..203
-FT   CDR1-IMGT           213..236
-FT                       /translation="GFTFDYYA"
-FT                       /AA_IMGT="AA 27 to 38, AA 31, 32, 33 and 34 are 
-FT                       missing"
-FT   FR2-IMGT            237..287
-FT                       /translation="MHWVRQAPGKGLEWVSG"
-FT                       /AA_IMGT="AA 39 to 55"
-FT   CONSERVED-TRP       243..245
-FT   CDR2-IMGT           288..311
-FT                       /translation="ITWNSGDM"
-FT                       /AA_IMGT="AA 56 to 65, AA 60 and 61 are missing"
-FT   FR3-IMGT            312..425
-FT                       /translation="GYADSVKGRFTISRDIAKNSLYLQMNSLRAEDTALYYC"
-FT                       /AA_IMGT="AA 66 to 104, AA 73 is missing"
-FT   2nd-CYS             423..425
-FT   CDR3-IMGT           426..464
-FT                       /translation="AKDQQQLFDSFDI"
-FT                       /AA_IMGT="AA 105 to 117"
-FT   JUNCTION            423..467
-FT                       /translation="CAKDQQQLFDSFDIW"
-FT                       /in_frame
-FT   3'V-REGION          423..433
-FT                       /translation="CAK"
-FT   (N-D)-J-REGION      434..497
-FT                       /codon_start=2
-FT                       /translation="QQQLFDSFDIWGQGTMVTVSS"
-FT   (N-D)-REGION        434..448
-FT                       /codon_start=2
-FT                       /translation="QQQL"
-FT   N1-REGION           434..435
-FT   D-J-REGION          436..497
-FT                       /codon_start=3
-FT                       /translation="QQLFDSFDIWGQGTMVTVSS"
-FT   D-REGION            436..445
-FT                       /codon_start=3
-FT                       /translation="QQ"
-FT                       /IMGT_allele="IGHD6-13*01"
-FT                       /IMGT_gene="IGHD6-13"
-FT   N2-REGION           446..448
-FT                       /codon_start=2
-FT   5'J-REGION          449..467
-FT   J-REGION            449..497
-FT                       /codon_start=2
-FT                       /translation="DSFDIWGQGTMVTVSS"
-FT                       /IMGT_allele="IGHJ3*02"
-FT                       /IMGT_gene="IGHJ3"
-FT   J-TRP               465..467
-FT   FR4-IMGT            465..497
-FT                       /translation="WGQGTMVTVSS"
-FT                       /AA_IMGT="AA 118 to 128"
-FT   C-REGION            498..1556
-FT                       /translation="ASPTSPKVFPLSLCSTQPDGNVVIACLVQGFFPQEPLSVTW
-FT                       SESGQGVTARNFPPSQDASGDLYTTSSQLTLPATQCLAGKSVTCHVKHYTNPSQD
-FT                       VTVPCPVPSTPPTPSPSTPPTPSPSCCHPRLSLHRPALEDLLLGSEANLTCTLTG
-FT                       LRDASGVTFTWTPSSGKSAVQGPPDRDLCGCYSVSSVLPGCAEPWNHGKTFTCTA
-FT                       AYPESKTPLTATLSKSGNTFRPEVHLLPPPSEELALNELVTLTCLARGFSPKDVL
-FT                       VRWLQGSQELPREKYLTWASRQEPSQGTTTFAVTSILRVAAEDWKKGDTFSCMVG
-FT                       HEALPLAFTQKTIDRLAGKPTHVNVSVVMAEVDGTCY"
-FT                       /IMGT_allele="IGHA1*01"
-FT                       /IMGT_gene="IGHA1"
-FT   STOP-CODON          1557..1559
-FT   3'UTR               1557..1603
-XX
-SQ   Sequence 1603 BP; 327 A; 526 C; 438 G; 312 T; 0 other;
-     agctctggga gaggagcccc agccctgaga ttcccaggtg tttccattca gtgatcagca        60
-     ctgaacacag aggactcacc atggagttgg gactgagctg gattttcctt ttggctattt       120
-     taaaaggtgt ccagtgtgaa gtgcaactgg tggagtctgg gggaggcttg gtacagcctg       180
-     gcaggcccct gagactctcc tgtgcagcct ctggattcac ctttgattat tatgccatgc       240
-     actgggtccg gcaagctcca gggaagggcc tggagtgggt ctcaggtatt acttggaata       300
-     gtggtgacat gggctatgcg gactctgtga agggccgatt caccatctcc agagacatcg       360
-     ccaagaactc cctgtatcta caaatgaaca gtctgagagc tgaggacacg gccttgtatt       420
-     actgtgcaaa agaccagcag cagctctttg attcttttga tatctggggc caagggacaa       480
-     tggtcactgt ctcttcagca tccccgacca gccccaaggt cttcccgctg agcctctgca       540
-     gcacccagcc agatgggaac gtggtcatcg cctgcctggt ccagggcttc ttcccccagg       600
-     agccactcag tgtgacctgg agcgaaagcg gacagggcgt gaccgccaga aacttcccac       660
-     ccagccagga tgcctccggg gacctgtaca ccacgagcag ccagctgacc ctgccggcca       720
-     cacagtgcct agccggcaag tccgtgacat gccacgtgaa gcactacacg aatcccagcc       780
-     aggatgtgac tgtgccctgc ccagttccct caactccacc taccccatct ccctcaactc       840
-     cacctacccc atctccctca tgctgccacc cccgactgtc actgcaccga ccggccctcg       900
-     aggacctgct cttaggttca gaagcgaacc tcacgtgcac actgaccggc ctgagagatg       960
-     cctcaggtgt caccttcacc tggacgccct caagtgggaa gagcgctgtt caaggaccac      1020
-     ctgaccgtga cctctgtggc tgctacagcg tgtccagtgt cctgccgggc tgtgccgagc      1080
-     catggaacca tgggaagacc ttcacttgca ctgctgccta ccccgagtcc aagaccccgc      1140
-     taaccgccac cctctcaaaa tccggaaaca cattccggcc cgaggtccac ctgctgccgc      1200
-     cgccgtcgga ggagctggcc ctgaacgagc tggtgacgct gacgtgcctg gcacgtggct      1260
-     tcagccccaa ggatgtgctg gttcgctggc tgcaggggtc acaggagctg ccccgcgaga      1320
-     agtacctgac ttgggcatcc cggcaggagc ccagccaggg caccaccacc ttcgctgtga      1380
-     ccagcatact gcgcgtggca gccgaggact ggaagaaggg ggacaccttc tcctgcatgg      1440
-     tgggccacga ggccctgccg ctggccttca cacagaagac catcgaccgc ttggcgggta      1500
-     aacccaccca tgtcaatgtg tctgttgtca tggcggaggt ggacggcacc tgctactgag      1560
-     ccgcccgcct gtccccaccc ctgaataaac tccatgctcc ccc                        1603
-//
-ID   AK128664; SV 1; linear; cDNA; STD; HUM; 1623 BP.
-XX
-AC   AK128664;
-XX
-DT   30-SEP-2003 (Rel. 200340-2, arrived in LIGM-DB)
-DT   15-JUN-2024 (Rel. 202424-6, Last updated, Version 9)
-XX
-DE   Homo sapiens cDNA FLJ46824 fis, clone TUTER2001433, highly similar to Ig
-DE   alpha-1 chain C region.
-XX
-KW   antigen receptor; Immunoglobulin superfamily (IgSF); immunoglobulin (IG);
-KW   IG-Heavy; IG-Heavy-Alpha; constant; IG-Heavy-Alpha-1-IGHA1; variable;
-KW   diversity; joining; regular; cDNA; undefined; rearranged; productive;
-KW   L-V-D-J-C-sequence.
-XX
-OS   Homo sapiens (human)
-OC   cellular organisms; Eukaryota; Opisthokonta; Metazoa; Eumetazoa; Bilateria;
-OC   Deuterostomia; Chordata; Craniata; Vertebrata; Gnathostomata; Teleostomi;
-OC   Euteleostomi; Sarcopterygii; Dipnotetrapodomorpha; Tetrapoda; Amniota;
-OC   Mammalia; Theria; Eutheria; Boreoeutheria; Euarchontoglires; Primates;
-OC   Haplorrhini; Simiiformes; Catarrhini; Hominoidea; Hominidae; Homininae;
-OC   Homo; Homo sapiens.
-XX
-RN   [1]
-RP   1-1623
-RA   Isogai T., Yamamoto J.;
-RT   ;
-RL   Submitted (15-JUL-2003) to the INSDC.
-RL   Contact:Takao Isogai Helix Research Institute, Genomics Laboratory; 1532-3
-RL   Yana, Kisarazu, Chiba 292-0812, Japan E-mail :flj-cdna@nifty.com
-XX
-RN   [2]
-RX   DOI; 10.1016/S0165-2478(97)00101-6.
-RX   PUBMED; 9373213.
-RA   Fukuoka M., Tokushima M., Koarada S., Sai T., Miyake K., Kimoto M.;
-RT   "Analysis of Vbeta4 T cell receptor CDR3 repertoire in BALB/c and (NZB x
-RT   NZW)F1 mice";
-RL   Immunol. Lett. 59(2):63-69(1997).
-XX
-DR   MD5; 9268d02b351c6db776a5a7694bac47c9.
-XX
-CC   IMGT/LIGM-DB annotation level: automatic
-CC
-CC   NEDO human cDNA sequencing project supported by Ministry of
-CC   Economy, Trade and Industry of Japan; cDNA full insert sequencing:
-CC   Research Association for Biotechnology (RAB); cDNA library
-CC   construction: Helix Research Institute (HRI) (supported by Japan
-CC   Key Technology Center etc.); 5'- & 3'-end one pass sequencing:
-CC   RAB, HRI, and Biotechnology Center, National Institute of
-CC   Technology and Evaluation; clone selection for full insert
-CC   sequencing: HRI and RAB; annotation: Reverse Proteomics Research
-CC   Institute, HRI and RAB.
-XX
-FH   Key                 Location/Qualifiers
-FH
-FT   L-V-D-J-C-SEQUENCE  1..1623
-FT                       /clone="TUTER2001433"
-FT                       /clone_lib="TUTER2"
-FT                       /db_xref="taxon:9606"
-FT                       /organism="Homo sapiens"
-FT                       /productive
-FT                       /tissue_type="uterus, tumor tissue"
-FT   L-V-D-J-C-REGION    80..1576
-FT                       /translation="MELGLYWVFLVAILEGVQCEVRLVESGGGFVQPGGSLRLSC
-FT                       AASGFTFSAHNMNWVRQAPGKGLEWISKISENGNTIYYANSVRGRFTVSRDNAQN
-FT                       TLYLQINRPREDDTAVYFCARDADVSGISVFWFFDLWGRGTLVNVSTVSSASPTS
-FT                       PKVFPLSLCSTQPDGNVVIACLVQGFFPQEPLSVTWSESGQGVTARNFPPSQDAS
-FT                       GDLYTTSSQLTLPATQCLAGKSVTCHVKHYTNPSQDVTVPCPVPSTPPTPSPSTP
-FT                       PTPSPSCCHPRLSLHRPALEDLLLGSEANLTCTLTGLRDASGVTFTWTPSSGKSA
-FT                       VQGPPERDLCGCYSVSSVLPGCAEPWNHGKTFTCTAAYPESKTPLTATLSKSGNT
-FT                       FRPEVHLLPPPSEELALNELVTLTCLARGFSPKDVLVRWLQGSQELPREKYLTWA
-FT                       SRQEPSQGTTTFAVTSILRVAAEDWKKGDTFSCMVGHEALPLAFTQKTIDRLAGK
-FT                       PTHVNVSVVMAEVDGTCY"
-FT                       /protein_id="BAC87558.1"
-FT   5'UTR               1..79
-FT   L-V-D-J-REGION      80..508
-FT                       /translation="MELGLYWVFLVAILEGVQCEVRLVESGGGFVQPGGSLRLSC
-FT                       AASGFTFSAHNMNWVRQAPGKGLEWISKISENGNTIYYANSVRGRFTVSRDNAQN
-FT                       TLYLQINRPREDDTAVYFCARDADVSGISVFWFFDLWGRGTLVNVST"
-FT   L-V-D-REGION        80..449
-FT                       /translation="MELGLYWVFLVAILEGVQCEVRLVESGGGFVQPGGSLRLSC
-FT                       AASGFTFSAHNMNWVRQAPGKGLEWISKISENGNTIYYANSVRGRFTVSRDNAQN
-FT                       TLYLQINRPREDDTAVYFCARDADVSG"
-FT   L-V-REGION          80..432
-FT                       /translation="MELGLYWVFLVAILEGVQCEVRLVESGGGFVQPGGSLRLSC
-FT                       AASGFTFSAHNMNWVRQAPGKGLEWISKISENGNTIYYANSVRGRFTVSRDNAQN
-FT                       TLYLQINRPREDDTAVYFCAR"
-FT   L-REGION            80..136
-FT                       /translation="MELGLYWVFLVAILEGVQC"
-FT   V-D-J-C-REGION      137..1576
-FT                       /translation="EVRLVESGGGFVQPGGSLRLSCAASGFTFSAHNMNWVRQAP
-FT                       GKGLEWISKISENGNTIYYANSVRGRFTVSRDNAQNTLYLQINRPREDDTAVYFC
-FT                       ARDADVSGISVFWFFDLWGRGTLVNVSTVSSASPTSPKVFPLSLCSTQPDGNVVI
-FT                       ACLVQGFFPQEPLSVTWSESGQGVTARNFPPSQDASGDLYTTSSQLTLPATQCLA
-FT                       GKSVTCHVKHYTNPSQDVTVPCPVPSTPPTPSPSTPPTPSPSCCHPRLSLHRPAL
-FT                       EDLLLGSEANLTCTLTGLRDASGVTFTWTPSSGKSAVQGPPERDLCGCYSVSSVL
-FT                       PGCAEPWNHGKTFTCTAAYPESKTPLTATLSKSGNTFRPEVHLLPPPSEELALNE
-FT                       LVTLTCLARGFSPKDVLVRWLQGSQELPREKYLTWASRQEPSQGTTTFAVTSILR
-FT                       VAAEDWKKGDTFSCMVGHEALPLAFTQKTIDRLAGKPTHVNVSVVMAEVDGTCY"
-FT   INIT-CODON          80..82
-FT   V-D-J-REGION        137..508
-FT                       /translation="EVRLVESGGGFVQPGGSLRLSCAASGFTFSAHNMNWVRQAP
-FT                       GKGLEWISKISENGNTIYYANSVRGRFTVSRDNAQNTLYLQINRPREDDTAVYFC
-FT                       ARDADVSGISVFWFFDLWGRGTLVNVST"
-FT                       /CDR_length="[8.8.17]"
-FT                       /FR_length="[25.17.38.11]"
-FT   V-REGION            137..432
-FT                       /translation="EVRLVESGGGFVQPGGSLRLSCAASGFTFSAHNMNWVRQAP
-FT                       GKGLEWISKISENGNTIYYANSVRGRFTVSRDNAQNTLYLQINRPREDDTAVYFC
-FT                       AR"
-FT                       /IMGT_allele="IGHV3-48*02"
-FT                       /IMGT_gene="IGHV3-48"
-FT                       /Videntity="85,47% (253/296 nt)"
-FT   FR1-IMGT            137..211
-FT                       /translation="EVRLVESGGGFVQPGGSLRLSCAAS"
-FT                       /AA_IMGT="AA 1 to 26, AA 10 is missing"
-FT   1st-CYS             200..202
-FT   CDR1-IMGT           212..235
-FT                       /translation="GFTFSAHN"
-FT                       /AA_IMGT="AA 27 to 38, AA 31, 32, 33 and 34 are 
-FT                       missing"
-FT   FR2-IMGT            236..286
-FT                       /translation="MNWVRQAPGKGLEWISK"
-FT                       /AA_IMGT="AA 39 to 55"
-FT   CONSERVED-TRP       242..244
-FT   CDR2-IMGT           287..310
-FT                       /translation="ISENGNTI"
-FT                       /AA_IMGT="AA 56 to 65, AA 60 and 61 are missing"
-FT   FR3-IMGT            311..424
-FT                       /translation="YYANSVRGRFTVSRDNAQNTLYLQINRPREDDTAVYFC"
-FT                       /AA_IMGT="AA 66 to 104, AA 73 is missing"
-FT   2nd-CYS             422..424
-FT   CDR3-IMGT           425..475
-FT                       /translation="ARDADVSGISVFWFFDL"
-FT                       /AA_IMGT="AA 105 to 117, AA 112.1, 111.1, 112.2 and 
-FT                       111.2 are added"
-FT   JUNCTION            422..478
-FT                       /translation="CARDADVSGISVFWFFDLW"
-FT                       /in_frame
-FT   3'V-REGION          422..432
-FT                       /translation="CAR"
-FT   (N-D)-J-REGION      433..508
-FT                       /codon_start=2
-FT                       /translation="ADVSGISVFWFFDLWGRGTLVNVST"
-FT   (N-D)-REGION        433..456
-FT                       /codon_start=2
-FT                       /translation="ADVSGIS"
-FT   P-REGION            433
-FT   N1-REGION           434..439
-FT                       /translation="AD"
-FT   D-J-REGION          440..508
-FT                       /translation="VSGISVFWFFDLWGRGTLVNVST"
-FT   D-REGION            440..449
-FT                       /translation="VSG"
-FT                       /IMGT_allele="IGHD6-19*01"
-FT                       /IMGT_gene="IGHD6-19"
-FT   N2-REGION           450..456
-FT                       /codon_start=3
-FT                       /translation="S"
-FT   5'J-REGION          457..478
-FT                       /translation="LLVLRSL"
-FT   J-REGION            457..508
-FT                       /codon_start=2
-FT                       /translation="FWFFDLWGRGTLVNVST"
-FT                       /IMGT_allele="IGHJ2*01"
-FT                       /IMGT_gene="IGHJ2"
-FT   J-TRP               476..478
-FT   FR4-IMGT            476..508
-FT                       /translation="WGRGTLVNVST"
-FT                       /AA_IMGT="AA 118 to 128"
-FT   C-REGION            509..1576
-FT                       /translation="VSSASPTSPKVFPLSLCSTQPDGNVVIACLVQGFFPQEPLS
-FT                       VTWSESGQGVTARNFPPSQDASGDLYTTSSQLTLPATQCLAGKSVTCHVKHYTNP
-FT                       SQDVTVPCPVPSTPPTPSPSTPPTPSPSCCHPRLSLHRPALEDLLLGSEANLTCT
-FT                       LTGLRDASGVTFTWTPSSGKSAVQGPPERDLCGCYSVSSVLPGCAEPWNHGKTFT
-FT                       CTAAYPESKTPLTATLSKSGNTFRPEVHLLPPPSEELALNELVTLTCLARGFSPK
-FT                       DVLVRWLQGSQELPREKYLTWASRQEPSQGTTTFAVTSILRVAAEDWKKGDTFSC
-FT                       MVGHEALPLAFTQKTIDRLAGKPTHVNVSVVMAEVDGTCY"
-FT                       /IMGT_allele="IGHA1*01"
-FT                       /IMGT_gene="IGHA1"
-FT   STOP-CODON          1577..1579
-FT   3'UTR               1577..1623
-XX
-SQ   Sequence 1623 BP; 324 A; 535 C; 449 G; 315 T; 0 other;
-     agctctcaga gaggtgcctt agccctggat cccaaggcat ttccacttgg tgatcagcac        60
-     tgaacacaga ggactcacca tggagttggg gctgtactgg gttttccttg ttgccatttt       120
-     agaaggtgtc cagtgtgagg tgcggttggt ggagtctggg ggaggcttcg tacagccggg       180
-     ggggtctctg agactctcct gtgcggcttc tggattcacc ttcagtgccc acaacatgaa       240
-     ctgggtccgc caggctccgg ggaagggact ggaatggatt tcaaagatta gtgaaaatgg       300
-     aaataccata tattacgcaa actctgtgag gggccgattc accgtctcca gggacaacgc       360
-     ccagaacaca ctgtatctgc aaattaacag gccgagagaa gacgacacgg ccgtatattt       420
-     ttgtgcgagg gatgcggatg tgtctggtat ctctgtcttc tggttcttcg atctctgggg       480
-     ccgtggcacc ctggtcaatg tctccactgt ctcctcagca tccccgacca gccccaaggt       540
-     cttcccgctg agcctctgca gcacccagcc agatgggaac gtggtcatcg cctgcctggt       600
-     ccagggcttc ttcccccagg agccactcag tgtgacctgg agcgaaagcg gacagggcgt       660
-     gaccgccaga aacttcccac ccagccagga tgcctccggg gacctgtaca ccacgagcag       720
-     ccagctgacc ctgccggcca cacagtgcct agccggcaag tccgtgacat gccacgtgaa       780
-     gcactacacg aatcccagcc aggatgtgac tgtgccctgc ccagttccct caactccacc       840
-     taccccatct ccctcaactc cacctacccc atctccctca tgctgccacc cccgactgtc       900
-     actgcaccga ccggccctcg aggacctgct cttaggttca gaagcgaacc tcacgtgcac       960
-     actgaccggc ctgagagatg cctcaggtgt caccttcacc tggacgccct caagtgggaa      1020
-     gagcgctgtt caaggaccac ctgagcgtga cctctgtggc tgctacagcg tgtccagtgt      1080
-     cctgccgggc tgtgccgagc catggaacca tgggaagacc ttcacttgca ctgctgccta      1140
-     ccccgagtcc aagaccccgc taaccgccac cctctcaaaa tccggaaaca cattccggcc      1200
-     cgaggtccac ctgctgccgc cgccgtcgga ggagctggcc ctgaacgagc tggtgacgct      1260
-     gacgtgcctg gcacgcggct tcagccccaa ggacgtgctg gttcgctggc tgcaggggtc      1320
-     acaggagctg ccccgcgaga agtacctgac ttgggcatcc cggcaggagc ccagccaggg      1380
-     caccaccacc ttcgctgtga ccagcatact gcgcgtggca gccgaggact ggaagaaggg      1440
-     ggacaccttc tcctgcatgg tgggccacga ggccctgccg ctggccttca cacagaagac      1500
-     catcgaccgc ttggcgggta aacccaccca tgtcaatgtg tctgttgtca tggcggaggt      1560
-     ggacggcacc tgctactgag ccgcccgcct gtccccaccc ctgaataaac tccatgctcc      1620
-     ccc                                                                    1623
-//
-ID   AY055778; SV 1; linear; cDNA; STD; MAM; 1619 BP.
-XX
-AC   AY055778;
-XX
-DT   21-DEC-2001 (Rel. 200151-5, arrived in LIGM-DB)
-DT   29-JUN-2024 (Rel. 202426-6, Last updated, Version 9)
-XX
-DE   Ornithorhynchus anatinus IgA1 immunoglobulin mRNA, complete cds.
-XX
-KW   antigen receptor; Immunoglobulin superfamily (IgSF); immunoglobulin (IG);
-KW   IG-Heavy; IG-Heavy-Alpha-1-IGHA1; variable; diversity; joining; regular;
-KW   cDNA; rearranged; productive; L-V-D-J-C-sequence.
-XX
-OS   Ornithorhynchus anatinus (platypus)
-OC   cellular organisms; Eukaryota; Opisthokonta; Metazoa; Eumetazoa; Bilateria;
-OC   Deuterostomia; Chordata; Craniata; Vertebrata; Gnathostomata; Teleostomi;
-OC   Euteleostomi; Sarcopterygii; Dipnotetrapodomorpha; Tetrapoda; Amniota;
-OC   Mammalia; Prototheria; Monotremata; Ornithorhynchidae; Ornithorhynchus;
-OC   Ornithorhynchus anatinus.
-XX
-RN   [1]
-RP   1-1619
-RA   Kimura A., Ohtani H., Nakajima T.;
-RT   ;
-RL   Submitted (23-DEC-2011) to the INSDC.
-RL   Contact:Hitoshi Ohtani Tokyo medical and dental university; yushima 1-5-45
-RL   MD tower 22F, Bunkyouku, Tokyo 113-8510, Japan
-XX
-RN   [2]
-RP   1-1619
-RA   Aveskogh M., Munday B., Hellman L.;
-RT   ;
-RL   Submitted (12-SEP-2001) to the INSDC.
-RL   Dept. of Cell and Molecular Biology, Uppsala University, BMC, Box 596,
-RL   Uppsala SE-75124, Sweden
-XX
-DR   EuropePMC; PMC3315531; 22479606.
-DR   EuropePMC; PMC3760800; 24019941.
-DR   EuropePMC; PMC4348116; 24676685.
-DR   MD5; 5fb98191549e495748477ec9ca4ac981.
-XX
-CC   IMGT/LIGM-DB annotation level: by annotators
-XX
-FH   Key                 Location/Qualifiers
-FH
-FT   L-V-D-J-C-SEQUENCE  1..1619
-FT                       /chromosome="4"
-FT                       /db_xref="taxon:9258"
-FT                       /mol_type="cDNA"
-FT                       /organism="Ornithorhynchus anatinus"
-FT   5'UTR               1..54
-FT   L-V-D-J-C-REGION    55..1494
-FT                       /translation="MRSALSLLSILTLLQGLQGDVQLVESGGDVRQPGGSLSLSC
-FT                       KASGFTFNNYFMYWIRQAPGKGLEWIAYISNSGGSTSYAGSVKGRFTISRDNSNS
-FT                       LVNLQMNSLKTDDTALYYCARASNCPDCAFEYWGQGTMVTVSSVDPKSPPVVFPL
-FT                       ETCSSENQDPVVVACLVKGIFPMPGVVYWDSDQASSFTRTYNSIQSTGGSFSFVS
-FT                       QLTMLSSQCPLEKEFHCTAIYNNLKATANVTCPPVPQCCKCSPKVLLHPPSLEGL
-FT                       FLGKGANLTCVLKGLVDPRETTFTWTRPNGDPSQATTGNPVEEEDGTYSLASVLE
-FT                       ICAEEWHQRDKFTCTVTHPKMSPITQTITKPPGPLNRPEVHLLAPSTEELALNEM
-FT                       ATLTCLVRGFNPPDLLVKWLKGGQEVSQTDYVTSSPQREASEGSASTFFLYSTLR
-FT                       VPTSEWKEGENYSCVVGHEALPLNFTQKTIDHSTGKPSTVNVSLVMSDTAGTCY"
-FT   L-V-D-J-REGION      55..471
-FT                       /translation="MRSALSLLSILTLLQGLQGDVQLVESGGDVRQPGGSLSLSC
-FT                       KASGFTFNNYFMYWIRQAPGKGLEWIAYISNSGGSTSYAGSVKGRFTISRDNSNS
-FT                       LVNLQMNSLKTDDTALYYCARASNCPDCAFEYWGQGTMVTVSS"
-FT   L-V-D-REGION        55..426
-FT                       /translation="MRSALSLLSILTLLQGLQGDVQLVESGGDVRQPGGSLSLSC
-FT                       KASGFTFNNYFMYWIRQAPGKGLEWIAYISNSGGSTSYAGSVKGRFTISRDNSNS
-FT                       LVNLQMNSLKTDDTALYYCARASNCPDC"
-FT   L-V-REGION          55..405
-FT                       /translation="MRSALSLLSILTLLQGLQGDVQLVESGGDVRQPGGSLSLSC
-FT                       KASGFTFNNYFMYWIRQAPGKGLEWIAYISNSGGSTSYAGSVKGRFTISRDNSNS
-FT                       LVNLQMNSLKTDDTALYYCAR"
-FT   L-REGION            55..111
-FT                       /translation="MRSALSLLSILTLLQGLQG"
-FT   INIT-CODON          55..57
-FT   V-D-J-C-REGION      112..1494
-FT                       /translation="DVQLVESGGDVRQPGGSLSLSCKASGFTFNNYFMYWIRQAP
-FT                       GKGLEWIAYISNSGGSTSYAGSVKGRFTISRDNSNSLVNLQMNSLKTDDTALYYC
-FT                       ARASNCPDCAFEYWGQGTMVTVSSVDPKSPPVVFPLETCSSENQDPVVVACLVKG
-FT                       IFPMPGVVYWDSDQASSFTRTYNSIQSTGGSFSFVSQLTMLSSQCPLEKEFHCTA
-FT                       IYNNLKATANVTCPPVPQCCKCSPKVLLHPPSLEGLFLGKGANLTCVLKGLVDPR
-FT                       ETTFTWTRPNGDPSQATTGNPVEEEDGTYSLASVLEICAEEWHQRDKFTCTVTHP
-FT                       KMSPITQTITKPPGPLNRPEVHLLAPSTEELALNEMATLTCLVRGFNPPDLLVKW
-FT                       LKGGQEVSQTDYVTSSPQREASEGSASTFFLYSTLRVPTSEWKEGENYSCVVGHE
-FT                       ALPLNFTQKTIDHSTGKPSTVNVSLVMSDTAGTCY"
-FT   V-D-J-REGION        112..471
-FT                       /translation="DVQLVESGGDVRQPGGSLSLSCKASGFTFNNYFMYWIRQAP
-FT                       GKGLEWIAYISNSGGSTSYAGSVKGRFTISRDNSNSLVNLQMNSLKTDDTALYYC
-FT                       ARASNCPDCAFEYWGQGTMVTVSS"
-FT                       /CDR_length="[8.8.2]"
-FT                       /FR_length="[26.17.38.X]"
-FT   V-D-REGION          112..426
-FT                       /translation="DVQLVESGGDVRQPGGSLSLSCKASGFTFNNYFMYWIRQAP
-FT                       GKGLEWIAYISNSGGSTSYAGSVKGRFTISRDNSNSLVNLQMNSLKTDDTALYYC
-FT                       ARASNCPDC"
-FT   V-REGION            112..405
-FT                       /translation="DVQLVESGGDVRQPGGSLSLSCKASGFTFNNYFMYWIRQAP
-FT                       GKGLEWIAYISNSGGSTSYAGSVKGRFTISRDNSNSLVNLQMNSLKTDDTALYYC
-FT                       AR"
-FT                       /CDR_length="[8.8.2]"
-FT                       /FR_length="[26.17.38.X]"
-FT   FR1-IMGT            112..186
-FT                       /translation="DVQLVESGGDVRQPGGSLSLSCKAS"
-FT                       /AA_IMGT="AA 1 to 26"
-FT   1st-CYS             175..177
-FT   CDR1-IMGT           187..210
-FT                       /translation="GFTFNNYF"
-FT                       /AA_IMGT="AA 27 to 38, AA 31, 32, 33 and 34 are 
-FT                       missing"
-FT   FR2-IMGT            211..261
-FT                       /translation="MYWIRQAPGKGLEWIAY"
-FT                       /AA_IMGT="AA 39 to 55"
-FT   CONSERVED-TRP       217..219
-FT   CDR2-IMGT           262..285
-FT                       /translation="ISNSGGST"
-FT                       /AA_IMGT="AA 56 to 65, AA 60 and 61 are missing"
-FT   FR3-IMGT            286..399
-FT                       /translation="SYAGSVKGRFTISRDNSNSLVNLQMNSLKTDDTALYYC"
-FT                       /AA_IMGT="AA 66 to 104, AA 73 is missing"
-FT   3'V-REGION          397..405
-FT                       /translation="CAR"
-FT   2nd-CYS             397..399
-FT   CDR3-IMGT           400..405
-FT                       /translation="AR"
-FT                       /AA_IMGT="AA 105 to 106"
-FT   D-REGION            406..426
-FT                       /translation="ASNCPDC"
-FT                       /functional
-FT                       /IMGT_allele="IGHD1*01 or IGHD2*01 or IGHD3*01"
-FT                       /IMGT_gene="IGHD1 or IGHD2 or IGHD3"
-FT   J-REGION            427..471
-FT                       /translation="AFEYWGQGTMVTVSS"
-FT                       /functional
-FT                       /IMGT_allele="IGHJ4*01"
-FT                       /IMGT_gene="IGHJ4"
-FT                       /Jidentity="80% (43/54 nt)"
-FT   5'J-REGION          427..441
-FT                       /translation="AFEYW"
-FT   J-TRP               439..441
-FT   C-REGION            472..1494
-FT                       /translation="VDPKSPPVVFPLETCSSENQDPVVVACLVKGIFPMPGVVYW
-FT                       DSDQASSFTRTYNSIQSTGGSFSFVSQLTMLSSQCPLEKEFHCTAIYNNLKATAN
-FT                       VTCPPVPQCCKCSPKVLLHPPSLEGLFLGKGANLTCVLKGLVDPRETTFTWTRPN
-FT                       GDPSQATTGNPVEEEDGTYSLASVLEICAEEWHQRDKFTCTVTHPKMSPITQTIT
-FT                       KPPGPLNRPEVHLLAPSTEELALNEMATLTCLVRGFNPPDLLVKWLKGGQEVSQT
-FT                       DYVTSSPQREASEGSASTFFLYSTLRVPTSEWKEGENYSCVVGHEALPLNFTQKT
-FT                       IDHSTGKPSTVNVSLVMSDTAGTCY"
-FT                       /db_xref="GI:17223799"
-FT                       /functional
-FT                       /IMGT_allele="IGHA1*01"
-FT                       /IMGT_gene="IGHA1"
-FT                       /protein_id="AAL17700.1"
-FT   CH1                 472..765
-FT                       /translation="VDPKSPPVVFPLETCSSENQDPVVVACLVKGIFPMPGVVYW
-FT                       DSDQASSFTRTYNSIQSTGGSFSFVSQLTMLSSQCPLEKEFHCTAIYNNLKATAN
-FT                       VT"
-FT   SPLICE-FIRST-CODON  472..474
-FT                       /splicing-frame="sf1"
-FT   H-CH2               766..1098
-FT                       /translation="CPPVPQCCKCSPKVLLHPPSLEGLFLGKGANLTCVLKGLVD
-FT                       PRETTFTWTRPNGDPSQATTGNPVEEEDGTYSLASVLEICAEEWHQRDKFTCTVT
-FT                       HPKMSPITQTITKPP"
-FT   SPLICE-FIRST-CODON  766..768
-FT                       /splicing-frame="sf1"
-FT   H                   766..783
-FT                       /translation="CPPVPQ"
-FT   CH2                 784..1098
-FT                       /translation="CCKCSPKVLLHPPSLEGLFLGKGANLTCVLKGLVDPRETTF
-FT                       TWTRPNGDPSQATTGNPVEEEDGTYSLASVLEICAEEWHQRDKFTCTVTHPKMSP
-FT                       ITQTITKPP"
-FT   CH3-CHS             1099..1494
-FT                       /translation="GPLNRPEVHLLAPSTEELALNEMATLTCLVRGFNPPDLLVK
-FT                       WLKGGQEVSQTDYVTSSPQREASEGSASTFFLYSTLRVPTSEWKEGENYSCVVGH
-FT                       EALPLNFTQKTIDHSTGKPSTVNVSLVMSDTAGTCY"
-FT   SPLICE-FIRST-CODON  1099..1101
-FT                       /splicing-frame="sf1"
-FT   CH3                 1099..1434
-FT                       /translation="GPLNRPEVHLLAPSTEELALNEMATLTCLVRGFNPPDLLVK
-FT                       WLKGGQEVSQTDYVTSSPQREASEGSASTFFLYSTLRVPTSEWKEGENYSCVVGH
-FT                       EALPLNFTQKTIDHST"
-FT   CHS                 1435..1494
-FT                       /translation="GKPSTVNVSLVMSDTAGTCY"
-FT                       /IMGT_note="For complete translation nucleotide G at 
-FT                       position 1494 has been included in CHS"
-FT   INT-DONOR-SPLICE    1435..1437
-FT   3'UTR               1495..1619
-FT   STOP-CODON          1495..1497
-XX
-SQ   Sequence 1619 BP; 372 A; 537 C; 403 G; 307 T; 0 other;
-     cgctgtctgt tccattcccc tcctgactcc aaaactgtca ctacgacccc caccatgcgg        60
-     tctgccctca gcctgctttc tatcctcacc ctgctccaag gacttcaggg tgatgttcag       120
-     ctggtggagt ccgggggaga tgtgagacag cctgggggat ccctgagcct ctcctgtaaa       180
-     gcctccggat tcaccttcaa caactacttc atgtactgga ttcgccaggc tccagggaag       240
-     gggctcgagt ggattgcata cataagtaat agtgggggca gcacaagtta cgcaggttcg       300
-     gtgaaaggtc gattcaccat ttccagggac aactccaaca gcctggtgaa tctgcagatg       360
-     aacagcctga aaaccgatga cacggccctt tattactgtg cgagagcgag taactgcccc       420
-     gactgtgctt tcgaatactg gggccaaggc accatggtca ccgtctcctc agttgatcca       480
-     aagtctcctc cagttgtgtt tcccctggaa acctgcagct cggagaacca ggaccctgtg       540
-     gtggttgcct gcctggtcaa agggatcttc ccaatgccag gggtggttta ctgggacagt       600
-     gaccaggctt cttccttcac ccgcacctac aactccatcc agtctaccgg tggaagcttc       660
-     agtttcgtga gccagctcac catgctctcc tcccagtgcc cgctggaaaa ggagttccac       720
-     tgcaccgcca tttacaacaa cttgaaagcc acggccaatg tgacatgccc acccgtacca       780
-     cagtgttgca agtgctctcc caaagtgctc ctgcaccccc cttccctgga agggctgttc       840
-     ctggggaaag gagccaatct gacctgcgtg ctcaagggcc tggtggaccc ccgagagacc       900
-     accttcacct ggacccgccc caacggagac ccctctcaag ccaccacggg gaatcctgtg       960
-     gaggaggagg acggcacata cagcttggcc agcgtcctgg agatctgcgc tgaggagtgg      1020
-     catcagagag ataaattcac ctgcaccgtg acccatccaa agatgtcccc gattacccaa      1080
-     accatcacca aaccaccagg ccccctgaac cggcccgagg tccacctgct ggccccctcc      1140
-     accgaggagc tggccctgaa tgagatggcc accctgacct gcctggtgag gggcttcaac      1200
-     cccccggacc tgctggtgaa gtggttgaag gggggacagg aggtgtccca gacggactac      1260
-     gtgaccagct ccccgcagcg ggaagccagc gagggctccg ccagcacatt cttcctgtac      1320
-     agcaccctcc gcgtcccgac ctccgaatgg aaagaggggg agaactactc ctgcgtggtg      1380
-     ggccacgagg ccctgcccct caacttcacc cagaaaacca tcgaccattc caccggcaaa      1440
-     cccagcactg tcaacgtgtc cctggtcatg tccgacaccg ccggtacctg ttactaagcc      1500
-     ccatcccccc tccgcctccc acgcctcagc ccccattctc tgtccagggg gacctgcacg      1560
-     agtcacctgc tcaataaacc atgatgcacc caaaaaaaaa aaaaaaaaaa aaaaaaaaa       1619
-//
\ No newline at end of file
diff --git a/rustyms-py/Cargo.toml b/rustyms-py/Cargo.toml
index d94a11e8..796bd46c 100644
--- a/rustyms-py/Cargo.toml
+++ b/rustyms-py/Cargo.toml
@@ -15,3 +15,6 @@ pyo3 = { workspace = true }
 rustyms = { path = "../rustyms" }
 ordered-float = { workspace = true }
 thin-vec = { workspace = true }
+
+[lints]
+workspace = true
diff --git a/rustyms-py/pyproject.toml b/rustyms-py/pyproject.toml
index ae30b047..fa125889 100644
--- a/rustyms-py/pyproject.toml
+++ b/rustyms-py/pyproject.toml
@@ -4,7 +4,7 @@ build-backend = "maturin"
 
 [project]
 name = "rustyms"
-requires-python = ">=3.11,<3.14"
+requires-python = ">=3.9,<3.14"
 classifiers = [
     "Intended Audience :: Science/Research",
     "Programming Language :: Rust",
diff --git a/rustyms-py/src/lib.rs b/rustyms-py/src/lib.rs
index e8d2793e..c54d8a41 100644
--- a/rustyms-py/src/lib.rs
+++ b/rustyms-py/src/lib.rs
@@ -347,7 +347,7 @@ impl MolecularFormula {
     }
 }
 
-/// A selection of ions that together define the charge of a peptide.
+/// A selection of ions that together define the charge of a peptidoform.
 #[pyclass]
 pub struct MolecularCharge(rustyms::MolecularCharge);
 
@@ -532,7 +532,7 @@ impl SimpleModification {
             &mut vec![],
             None,
         ) {
-            Ok(modification) => Ok(SimpleModification(modification.defined().unwrap())),
+            Ok((modification, _)) => Ok(SimpleModification(modification.defined().unwrap())),
             Err(_) => Err(PyValueError::new_err("Invalid modification")),
         }
     }
@@ -608,7 +608,7 @@ impl Modification {
     }
 }
 
-/// A theoretical fragment of a peptide.
+/// A theoretical fragment of a peptidoform.
 #[pyclass]
 #[derive(Debug)]
 pub struct Fragment(rustyms::Fragment);
@@ -617,12 +617,12 @@ pub struct Fragment(rustyms::Fragment);
 impl Fragment {
     fn __repr__(&self) -> String {
         format!(
-            "Fragment(formula='{:?}', charge={}, ion='{}', peptidoform_index={}, peptide_index={}, neutral_loss='{:?}')",
+            "Fragment(formula='{:?}', charge={}, ion='{}', peptidoform_ion_index={}, peptidoform_index={}, neutral_loss='{:?}')",
             Self::formula(self),
             self.charge(),
             self.ion().0,
+            self.peptidoform_ion_index().map_or("-".to_string(), |p| p.to_string()),
             self.peptidoform_index().map_or("-".to_string(), |p| p.to_string()),
-            self.peptide_index().map_or("-".to_string(), |p| p.to_string()),
             self.neutral_loss(),
         )
     }
@@ -660,15 +660,26 @@ impl Fragment {
         FragmentType(self.0.ion.clone())
     }
 
-    /// The peptide this fragment comes from, saved as the index into the list of peptides in the overarching crate::ComplexPeptide struct.
+    /// The peptidoform this fragment comes from, saved as the index into the list of peptidoforms in the overarching crate::PeptidoformIon struct.
     ///
     /// Returns
     /// -------
     /// int | None
     ///
     #[getter]
-    fn peptide_index(&self) -> Option<usize> {
-        self.0.peptide_index
+    fn peptidoform_index(&self) -> Option<usize> {
+        self.0.peptidoform_index
+    }
+
+    /// The peptidoform ion this fragment comes from, saved as the index into the list of peptidoform ions in the overarching crate::CompoundPeptidoformIon struct.
+    ///
+    /// Returns
+    /// -------
+    /// int | None
+    ///
+    #[getter]
+    fn peptidoform_ion_index(&self) -> Option<usize> {
+        self.0.peptidoform_ion_index
     }
 
     /// The peptidoform this fragment comes from, saved as the index into the list of peptides in the overarching crate::ComplexPeptide struct.
@@ -827,7 +838,7 @@ impl SequencePosition {
         matches!(self, SequencePosition(rustyms::SequencePosition::CTerm))
     }
 }
-/// A compound peptidoform with all data as provided by ProForma 2.0.
+/// A compound peptidoform ion with all data as provided by ProForma 2.0.
 ///
 /// Parameters
 /// ----------
@@ -836,46 +847,46 @@ impl SequencePosition {
 ///
 #[pyclass]
 #[derive(Clone)]
-pub struct CompoundPeptidoform(rustyms::CompoundPeptidoform);
+pub struct CompoundPeptidoformIon(rustyms::CompoundPeptidoformIon);
 
 #[pymethods]
-impl CompoundPeptidoform {
-    /// Create a new peptide from a ProForma string.
+impl CompoundPeptidoformIon {
+    /// Create a new compound peptidoform ion from a ProForma string.
     #[new]
     fn new(proforma: &str) -> Result<Self, CustomError> {
-        rustyms::CompoundPeptidoform::pro_forma(proforma, None)
-            .map(CompoundPeptidoform)
+        rustyms::CompoundPeptidoformIon::pro_forma(proforma, None)
+            .map(CompoundPeptidoformIon)
             .map_err(CustomError)
     }
 
-    /// Create a new peptide from a peptidoform.
+    /// Create a new compound peptidoform ion from a peptidoform ion.
     #[staticmethod]
-    fn from_peptidoform(peptidoform: Peptidoform) -> Self {
-        CompoundPeptidoform(peptidoform.0.into())
+    fn from_peptidoform_ion(peptidoform: PeptidoformIon) -> Self {
+        CompoundPeptidoformIon(peptidoform.0.into())
     }
 
-    /// Create a new peptide from a linear peptide.
+    /// Create a new compound peptidoform ion from a peptidoform.
     #[staticmethod]
-    fn from_peptide(peptide: LinearPeptide) -> Self {
-        CompoundPeptidoform(peptide.0.into())
+    fn from_peptidoform(peptidoform: Peptidoform) -> Self {
+        CompoundPeptidoformIon(peptidoform.0.into())
     }
 
-    /// Get all peptidoforms making up this compound peptidoform.
+    /// Get all peptidoform ions making up this compound peptidoform.
     ///
     /// Returns
     /// -------
-    /// List[Peptidoform]
+    /// List[PeptidoformIon]
     ///
     #[getter]
-    fn peptidoforms(&self) -> Vec<Peptidoform> {
+    fn peptidoform_ions(&self) -> Vec<PeptidoformIon> {
         self.0
-            .peptidoforms()
+            .peptidoform_ions()
             .iter()
-            .map(|p| Peptidoform(p.clone()))
+            .map(|p| PeptidoformIon(p.clone()))
             .collect()
     }
 
-    /// Generate the theoretical fragments for this compound peptidoform, with the given maximal charge of the fragments,
+    /// Generate the theoretical fragments for this compound peptidoform ion, with the given maximal charge of the fragments,
     /// and the given model. With the global isotope modifications applied.
     ///
     /// Parameters
@@ -911,15 +922,15 @@ impl CompoundPeptidoform {
     }
 
     fn __repr__(&self) -> String {
-        format!("CompoundPeptidoform({})", self.0)
+        format!("CompoundPeptidoformIon({})", self.0)
     }
 
     fn __len__(&self) -> usize {
-        self.0.peptidoforms().len()
+        self.0.peptidoform_ions().len()
     }
 }
 
-/// A peptidoform with all data as provided by ProForma 2.0.
+/// A peptidoform ion with all data as provided by ProForma 2.0.
 ///
 /// Parameters
 /// ----------
@@ -928,40 +939,40 @@ impl CompoundPeptidoform {
 ///
 #[pyclass]
 #[derive(Clone)]
-pub struct Peptidoform(rustyms::Peptidoform);
+pub struct PeptidoformIon(rustyms::PeptidoformIon);
 
 #[pymethods]
-impl Peptidoform {
-    /// Create a new peptidoform from a ProForma string. Panics
+impl PeptidoformIon {
+    /// Create a new peptidoform ion from a ProForma string. Panics
     #[new]
     fn new(proforma: &str) -> Result<Self, CustomError> {
-        rustyms::Peptidoform::pro_forma(proforma, None)
-            .map(Peptidoform)
+        rustyms::PeptidoformIon::pro_forma(proforma, None)
+            .map(PeptidoformIon)
             .map_err(CustomError)
     }
 
-    /// Create a new peptidoform from a linear peptide.
+    /// Create a new peptidoform ion from a peptidoform.
     #[staticmethod]
-    fn from_peptide(peptide: LinearPeptide) -> Self {
-        Peptidoform(peptide.0.clone().into())
+    fn from_peptidoform(peptidoform: Peptidoform) -> Self {
+        PeptidoformIon(peptidoform.0.clone().into())
     }
 
-    /// Get all peptides making up this peptidoform.
+    /// Get all peptidoforms making up this peptidoform ion.
     ///
     /// Returns
     /// -------
-    /// List[LinearPeptide]
+    /// List[Peptidoform]
     ///
     #[getter]
-    fn peptides(&self) -> Vec<LinearPeptide> {
+    fn peptidoforms(&self) -> Vec<Peptidoform> {
         self.0
-            .peptides()
+            .peptidoforms()
             .iter()
-            .map(|p| LinearPeptide(p.clone()))
+            .map(|p| Peptidoform(p.clone()))
             .collect()
     }
 
-    /// Generate the theoretical fragments for this peptidoform, with the given maximal charge of the fragments,
+    /// Generate the theoretical fragments for this peptidoform ion, with the given maximal charge of the fragments,
     /// and the given model. With the global isotope modifications applied.
     ///
     /// Parameters
@@ -997,15 +1008,15 @@ impl Peptidoform {
     }
 
     fn __repr__(&self) -> String {
-        format!("Peptidoform({})", self.0)
+        format!("PeptidoformIon({})", self.0)
     }
 
     fn __len__(&self) -> usize {
-        self.0.peptides().len()
+        self.0.peptidoforms().len()
     }
 }
 
-/// A peptide with all data as provided by ProForma 2.0.
+/// A peptidoform with all data as provided by ProForma 2.0.
 ///
 /// Parameters
 /// ----------
@@ -1014,15 +1025,15 @@ impl Peptidoform {
 ///
 #[pyclass]
 #[derive(Clone)]
-pub struct LinearPeptide(rustyms::LinearPeptide<Linked>);
+pub struct Peptidoform(rustyms::Peptidoform<Linked>);
 
 #[pymethods]
-impl LinearPeptide {
-    /// Create a new peptide from a ProForma string.
+impl Peptidoform {
+    /// Create a new peptidoform from a ProForma string.
     #[new]
     fn new(proforma: &str) -> Result<Self, CustomError> {
-        rustyms::LinearPeptide::pro_forma(proforma, None)
-            .map(LinearPeptide)
+        rustyms::Peptidoform::pro_forma(proforma, None)
+            .map(Peptidoform)
             .map_err(CustomError)
     }
 
@@ -1031,7 +1042,7 @@ impl LinearPeptide {
     }
 
     fn __repr__(&self) -> String {
-        format!("LinearPeptide({})", self.0)
+        format!("Peptidoform({})", self.0)
     }
 
     fn __len__(&self) -> usize {
@@ -1057,25 +1068,33 @@ impl LinearPeptide {
     ///
     /// Returns
     /// -------
-    /// Modification | None
+    /// list[Modification]
     ///
     #[getter]
-    fn n_term(&self) -> Option<Modification> {
-        self.0.get_n_term().map(|m| Modification(m.clone()))
+    fn n_term(&self) -> Vec<Modification> {
+        self.0
+            .get_n_term()
+            .iter()
+            .map(|m| Modification(m.clone()))
+            .collect()
     }
 
     /// C-terminal modification.
     ///
     /// Returns
     /// -------
-    /// Modification | None
+    /// list[Modification]
     ///
     #[getter]
-    fn c_term(&self) -> Option<Modification> {
-        self.0.get_c_term().map(|m| Modification(m.clone()))
+    fn c_term(&self) -> Vec<Modification> {
+        self.0
+            .get_c_term()
+            .iter()
+            .map(|m| Modification(m.clone()))
+            .collect()
     }
 
-    /// Sequence of the peptide including modifications.
+    /// Sequence of the peptidoform including modifications.
     ///
     /// Returns
     /// -------
@@ -1120,7 +1139,7 @@ impl LinearPeptide {
             .collect()
     }
 
-    /// The precursor charge of the peptide.
+    /// The precursor charge of the peptidoform.
     ///
     /// Returns
     /// -------
@@ -1144,17 +1163,17 @@ impl LinearPeptide {
             .map(|c| MolecularCharge(c.clone()))
     }
 
-    /// Get a copy of the peptide with its sequence reversed.
+    /// Get a copy of the peptidoform with its sequence reversed.
     ///
     /// Returns
     /// -------
-    /// LinearPeptide
+    /// Peptidoform
     ///
-    fn reverse(&self) -> LinearPeptide {
-        LinearPeptide(self.0.reverse())
+    fn reverse(&self) -> Peptidoform {
+        Peptidoform(self.0.reverse())
     }
 
-    /// Gives the formulas for the whole peptide. With the global isotope modifications applied. (Any B/Z will result in multiple possible formulas.)
+    /// Gives the formulas for the whole peptidoform. With the global isotope modifications applied. (Any B/Z will result in multiple possible formulas.)
     ///
     /// Returns
     /// -------
@@ -1169,7 +1188,7 @@ impl LinearPeptide {
         })
     }
 
-    /// Generate the theoretical fragments for this peptide, with the given maximal charge of the fragments, and the given model. With the global isotope modifications applied.
+    /// Generate the theoretical fragments for this peptidoform, with the given maximal charge of the fragments, and the given model. With the global isotope modifications applied.
     ///
     /// Parameters
     /// ----------
@@ -1471,12 +1490,12 @@ impl RawSpectrum {
         self.0.clone().into_iter().map(RawPeak).collect()
     }
 
-    /// Annotate this spectrum with the given peptide
+    /// Annotate this spectrum with the given peptidoform
     ///
     /// Parameters
     /// ----------
-    /// peptide : CompoundPeptide
-    ///     The peptide to annotate the spectrum with.
+    /// peptidoform : CompoundPeptidoformIon
+    ///     The peptidoform to annotate the spectrum with.
     /// model : FragmentationModel
     ///     The model to use for the fragmentation.
     /// mode : MassMode
@@ -1492,22 +1511,22 @@ impl RawSpectrum {
     /// ValueError
     ///     If the model is not one of the valid models.
     ///
-    #[pyo3(signature = (peptide, model, mode=&MassMode::Monoisotopic))]
+    #[pyo3(signature = (peptidoform, model, mode=&MassMode::Monoisotopic))]
     fn annotate(
         &self,
-        peptide: CompoundPeptidoform,
+        peptidoform: CompoundPeptidoformIon,
         model: &FragmentationModel,
         mode: &MassMode,
     ) -> PyResult<AnnotatedSpectrum> {
         let rusty_model = match_model(model)?;
-        let fragments = peptide.0.generate_theoretical_fragments(
+        let fragments = peptidoform.0.generate_theoretical_fragments(
             self.0
                 .charge
                 .unwrap_or(rustyms::system::usize::Charge::new::<rustyms::system::e>(1)),
             &rusty_model,
         );
         Ok(AnnotatedSpectrum(self.0.annotate(
-            peptide.0,
+            peptidoform.0,
             &fragments,
             &rusty_model,
             match mode {
@@ -1614,18 +1633,18 @@ fn rustyms_py03(_py: Python, m: &Bound<'_, PyModule>) -> PyResult<()> {
     m.add_class::<AminoAcid>()?;
     m.add_class::<AnnotatedPeak>()?;
     m.add_class::<AnnotatedSpectrum>()?;
-    m.add_class::<CompoundPeptidoform>()?;
+    m.add_class::<CompoundPeptidoformIon>()?;
     m.add_class::<CustomError>()?;
     m.add_class::<Element>()?;
     m.add_class::<Fragment>()?;
     m.add_class::<FragmentationModel>()?;
     m.add_class::<FragmentType>()?;
-    m.add_class::<LinearPeptide>()?;
+    m.add_class::<Peptidoform>()?;
     m.add_class::<MassMode>()?;
     m.add_class::<Modification>()?;
     m.add_class::<MolecularCharge>()?;
     m.add_class::<MolecularFormula>()?;
-    m.add_class::<Peptidoform>()?;
+    m.add_class::<PeptidoformIon>()?;
     m.add_class::<RawPeak>()?;
     m.add_class::<RawSpectrum>()?;
     m.add_class::<SequenceElement>()?;
diff --git a/rustyms/Cargo.toml b/rustyms/Cargo.toml
index 38cf889c..c15bd34c 100644
--- a/rustyms/Cargo.toml
+++ b/rustyms/Cargo.toml
@@ -58,5 +58,5 @@ isotopes = ["probability", "ndarray"]
 name = "iai"
 harness = false
 
-[lints.rust]
-unexpected_cfgs = { level = "warn", check-cfg = ['cfg(github_action)'] }
+[lints]
+workspace = true
diff --git a/rustyms/README.md b/rustyms/README.md
index 27a649ac..05b0fe3d 100644
--- a/rustyms/README.md
+++ b/rustyms/README.md
@@ -33,7 +33,7 @@ use rustyms::{*, system::{usize::Charge, e}};
 // Open example raw data (this is the built in mgf reader, look into mzdata for more advanced raw file readers)
 let spectrum = rawfile::mgf::open(raw_file_path)?;
 // Parse the given ProForma definition
-let peptide = CompoundPeptidoform::pro_forma("[Gln->pyro-Glu]-QVQEVSERTHGGNFD", None)?;
+let peptide = CompoundPeptidoformIon::pro_forma("[Gln->pyro-Glu]-QVQEVSERTHGGNFD", None)?;
 // Generate theoretical fragments for this peptide given EThcD fragmentation
 let model = Model::ethcd();
 let fragments = peptide.generate_theoretical_fragments(Charge::new::<e>(2), &model);
@@ -51,8 +51,8 @@ assert!(fdr.peaks_sigma() > 2.0);
 # fn main() -> Result<(), rustyms::error::CustomError> {
 use rustyms::{*, align::*};
 // Check how this peptide compares to a similar peptide (using the feature `align`)
-let first_peptide = LinearPeptide::pro_forma("IVQEVT", None)?.into_simple_linear().unwrap();
-let second_peptide = LinearPeptide::pro_forma("LVQVET", None)?.into_simple_linear().unwrap();
+let first_peptide = Peptidoform::pro_forma("IVQEVT", None)?.into_simple_linear().unwrap();
+let second_peptide = Peptidoform::pro_forma("LVQVET", None)?.into_simple_linear().unwrap();
 // Align the two peptides using mass based alignment
 // IVQEVT A
 // LVQVET B
diff --git a/rustyms/benches/iai.rs b/rustyms/benches/iai.rs
index d1d47497..30d04b85 100644
--- a/rustyms/benches/iai.rs
+++ b/rustyms/benches/iai.rs
@@ -9,14 +9,14 @@ use iai_callgrind::{
 };
 
 #[inline(never)]
-fn setup(a: &str, b: &str) -> (LinearPeptide<SimpleLinear>, LinearPeptide<SimpleLinear>) {
+fn setup(a: &str, b: &str) -> (Peptidoform<SimpleLinear>, Peptidoform<SimpleLinear>) {
     let _force_elements_init = black_box(AminoAcid::Alanine.formulas());
     (
-        LinearPeptide::pro_forma(a, None)
+        Peptidoform::pro_forma(a, None)
             .unwrap()
             .into_simple_linear()
             .unwrap(),
-        LinearPeptide::pro_forma(b, None)
+        Peptidoform::pro_forma(b, None)
             .unwrap()
             .into_simple_linear()
             .unwrap(),
@@ -24,19 +24,19 @@ fn setup(a: &str, b: &str) -> (LinearPeptide<SimpleLinear>, LinearPeptide<Simple
 }
 
 #[inline(never)]
-fn setup_simple() -> (LinearPeptide<SimpleLinear>, LinearPeptide<SimpleLinear>) {
+fn setup_simple() -> (Peptidoform<SimpleLinear>, Peptidoform<SimpleLinear>) {
     setup("ANAGRS", "AGGQRS")
 }
 
 #[inline(never)]
-fn setup_igha() -> (LinearPeptide<SimpleLinear>, LinearPeptide<SimpleLinear>) {
+fn setup_igha() -> (Peptidoform<SimpleLinear>, Peptidoform<SimpleLinear>) {
     setup("ASPTSPKVFPLSLDSTPQDGNVVVACLVQGFFPQEPLSVTWSESGQNVTARNFPPSQDASGDLYTTSSQLTLPATQCPDGKSVTCHVKHYTNSSQDVTVPCRVPPPPPCCHPRLSLHRPALEDLLLGSEANLTCTLTGLRDASGATFTWTPSSGKSAVQGPPERDLCGCYSVSSVLPGCAQPWNHGETFTCTAAHPELKTPLTANITKSGNTFRPEVHLLPPPSEELALNELVTLTCLARGFSPKDVLVRWLQGSQELPREKYLTWASRQEPSQGTTTYAVTSILRVAAEDWKKGETFSCMVGHEALPLAFTQKTIDRMAGSCCVADWQMPPPYVVLDLPQETLEEETPGANLWPTTITFLTLFLLSLFYSTALTVTSVRGPSGKREGPQY", "ASPTSPKVFPLSLCSTQPDGNVVIACLVQGFFPQEPLSVTWSESGQGVTARNFPPSQDASGDLYTTSSQLTLPATQCLAGKSVTCHVKHYTNPSQDVTVPCPVPSTPPTPSPSTPPTPSPSCCHPRLSLHRPALEDLLLGSEANLTCTLTGLRDASGVTFTWTPSSGKSAVQGPPERDLCGCYSVSSVLPGCAEPWNHGKTFTCTAAYPESKTPLTATLSKSGNTFRPEVHLLPPPSEELALNELVTLTCLARGFSPKDVLVRWLQGSQELPREKYLTWASRQEPSQGTTTFAVTSILRVAAEDWKKGDTFSCMVGHEALPLAFTQKTIDRLADWQMPPPYVVLDLPQETLEEETPGANLWPTTITFLTLFLLSLFYSTALTVTSVRGPSGNREGPQY")
 }
 
 #[library_benchmark]
 #[bench::simple_1(setup_simple())]
 #[bench::igha_1(setup_igha())]
-pub fn align_1(setup: (LinearPeptide<SimpleLinear>, LinearPeptide<SimpleLinear>)) {
+pub fn align_1(setup: (Peptidoform<SimpleLinear>, Peptidoform<SimpleLinear>)) {
     align::<1, SimpleLinear, SimpleLinear>(
         &setup.0,
         &setup.1,
@@ -53,7 +53,7 @@ pub fn align_1(setup: (LinearPeptide<SimpleLinear>, LinearPeptide<SimpleLinear>)
 #[bench::ambiguous_b(setup("ANQRS", "ABQRS"))]
 #[bench::ambiguous_ab(setup("ANZRS", "ABQRS"))]
 // #[bench::igha_8(setup_igha(Some(8)))]
-pub fn align_4(setup: (LinearPeptide<SimpleLinear>, LinearPeptide<SimpleLinear>)) {
+pub fn align_4(setup: (Peptidoform<SimpleLinear>, Peptidoform<SimpleLinear>)) {
     align::<4, SimpleLinear, SimpleLinear>(
         &setup.0,
         &setup.1,
@@ -65,7 +65,7 @@ pub fn align_4(setup: (LinearPeptide<SimpleLinear>, LinearPeptide<SimpleLinear>)
 #[library_benchmark]
 #[bench::simple_unbounded(setup_simple())]
 // #[bench::igha_8(setup_igha(Some(8)))]
-pub fn align_unbounded(setup: (LinearPeptide<SimpleLinear>, LinearPeptide<SimpleLinear>)) {
+pub fn align_unbounded(setup: (Peptidoform<SimpleLinear>, Peptidoform<SimpleLinear>)) {
     align::<{ u16::MAX }, SimpleLinear, SimpleLinear>(
         &setup.0,
         &setup.1,
diff --git a/rustyms/src/align/alignment.rs b/rustyms/src/align/alignment.rs
index f7e55f26..3375a4fd 100644
--- a/rustyms/src/align/alignment.rs
+++ b/rustyms/src/align/alignment.rs
@@ -14,23 +14,23 @@ use super::scoring::*;
 use crate::align::mass_alignment::determine_final_score;
 use crate::align::mass_alignment::score_pair;
 use crate::helper_functions::next_num;
-use crate::peptide::AtMax;
-use crate::peptide::Linear;
+use crate::peptidoform::AtMax;
+use crate::peptidoform::Linear;
 use crate::system::Mass;
 use crate::system::Ratio;
-use crate::LinearPeptide;
 use crate::MolecularFormula;
 use crate::Multi;
+use crate::Peptidoform;
 use crate::SequencePosition;
 use crate::SimpleLinear;
 
 /// An alignment of two reads. It has either a reference to the two sequences to prevent overzealous use of memory, or if needed use [`Self::to_owned`] to get a variant that clones the sequences and so can be used in more places.
-#[derive(Debug)]
+#[derive(Debug, Serialize, Deserialize)]
 pub struct Alignment<'lifetime, A, B> {
     /// The first sequence
-    pub(super) seq_a: Cow<'lifetime, LinearPeptide<A>>,
+    pub(super) seq_a: Cow<'lifetime, Peptidoform<A>>,
     /// The second sequence
-    pub(super) seq_b: Cow<'lifetime, LinearPeptide<B>>,
+    pub(super) seq_b: Cow<'lifetime, Peptidoform<B>>,
     /// The scores of this alignment
     pub(super) score: Score,
     /// The path or steps taken for the alignment
@@ -45,7 +45,7 @@ pub struct Alignment<'lifetime, A, B> {
     pub(super) maximal_step: u16,
 }
 
-impl<'lifetime, A, B> Clone for Alignment<'lifetime, A, B> {
+impl<A, B> Clone for Alignment<'_, A, B> {
     fn clone(&self) -> Self {
         Self {
             seq_a: self.seq_a.clone(),
@@ -60,7 +60,7 @@ impl<'lifetime, A, B> Clone for Alignment<'lifetime, A, B> {
     }
 }
 
-impl<'lifetime, A, B> PartialEq for Alignment<'lifetime, A, B> {
+impl<A, B> PartialEq for Alignment<'_, A, B> {
     fn eq(&self, other: &Self) -> bool {
         self.seq_a == other.seq_a
             && self.seq_b == other.seq_b
@@ -73,7 +73,7 @@ impl<'lifetime, A, B> PartialEq for Alignment<'lifetime, A, B> {
     }
 }
 
-impl<'lifetime, A, B> std::hash::Hash for Alignment<'lifetime, A, B> {
+impl<A, B> std::hash::Hash for Alignment<'_, A, B> {
     fn hash<H: std::hash::Hasher>(&self, state: &mut H) {
         self.seq_a.hash(state);
         self.seq_b.hash(state);
@@ -86,9 +86,9 @@ impl<'lifetime, A, B> std::hash::Hash for Alignment<'lifetime, A, B> {
     }
 }
 
-impl<'lifetime, A, B> Eq for Alignment<'lifetime, A, B> {}
+impl<A, B> Eq for Alignment<'_, A, B> {}
 
-impl<'lifetime, A, B> Alignment<'lifetime, A, B> {
+impl<A, B> Alignment<'_, A, B> {
     /// Clone the referenced sequences to make an alignment that owns the sequences.
     /// This can be necessary in some context where the references cannot be guaranteed to stay as long as you need the alignment.
     #[must_use]
@@ -101,13 +101,13 @@ impl<'lifetime, A, B> Alignment<'lifetime, A, B> {
     }
 }
 
-impl<'lifetime, A, B> PartialOrd for Alignment<'lifetime, A, B> {
+impl<A, B> PartialOrd for Alignment<'_, A, B> {
     fn partial_cmp(&self, other: &Self) -> Option<std::cmp::Ordering> {
         Some(self.cmp(other))
     }
 }
 
-impl<'lifetime, A, B> Ord for Alignment<'lifetime, A, B> {
+impl<A, B> Ord for Alignment<'_, A, B> {
     fn cmp(&self, other: &Self) -> std::cmp::Ordering {
         self.score.normalised.cmp(&other.score.normalised)
     }
@@ -115,10 +115,10 @@ impl<'lifetime, A, B> Ord for Alignment<'lifetime, A, B> {
 
 impl<'lifetime, A: AtMax<SimpleLinear>, B: AtMax<SimpleLinear>> Alignment<'lifetime, A, B> {
     /// Recreate an alignment from a path, the path is [`Self::short`].
-    #[allow(clippy::missing_panics_doc)]
+    #[expect(clippy::missing_panics_doc)]
     pub fn create_from_path(
-        seq_a: &'lifetime LinearPeptide<A>,
-        seq_b: &'lifetime LinearPeptide<B>,
+        seq_a: &'lifetime Peptidoform<A>,
+        seq_b: &'lifetime Peptidoform<B>,
         start_a: usize,
         start_b: usize,
         path: &str,
@@ -285,13 +285,13 @@ impl<'lifetime, A: AtMax<SimpleLinear>, B: AtMax<SimpleLinear>> Alignment<'lifet
     }
 }
 
-impl<'lifetime, A, B> Alignment<'lifetime, A, B> {
+impl<A, B> Alignment<'_, A, B> {
     /// The first sequence
-    pub fn seq_a(&self) -> &LinearPeptide<A> {
+    pub fn seq_a(&self) -> &Peptidoform<A> {
         &self.seq_a
     }
     /// The second sequence
-    pub fn seq_b(&self) -> &LinearPeptide<B> {
+    pub fn seq_b(&self) -> &Peptidoform<B> {
         &self.seq_b
     }
 
@@ -383,7 +383,7 @@ impl<'lifetime, A, B> Alignment<'lifetime, A, B> {
     }
 }
 
-impl<'lifetime, A: AtMax<Linear>, B: AtMax<Linear>> Alignment<'lifetime, A, B> {
+impl<A: AtMax<Linear>, B: AtMax<Linear>> Alignment<'_, A, B> {
     /// The mass(es) for the matched portion of the first sequence TODO: this assumes no terminal mods
     pub fn mass_a(&self) -> Multi<MolecularFormula> {
         if self.align_type().left.global_a() && self.align_type().right.global_a() {
@@ -436,7 +436,7 @@ impl<'lifetime, A: AtMax<Linear>, B: AtMax<Linear>> Alignment<'lifetime, A, B> {
 
     /// Get the mass delta for this match, if it is a (partial) local match it will only take the matched amino acids into account.
     /// If there are multiple possible masses for any of the stretches it returns the smallest difference.
-    #[allow(clippy::missing_panics_doc)]
+    #[expect(clippy::missing_panics_doc)]
     pub fn mass_difference(&self) -> Mass {
         self.mass_a()
             .iter()
@@ -448,7 +448,7 @@ impl<'lifetime, A: AtMax<Linear>, B: AtMax<Linear>> Alignment<'lifetime, A, B> {
 
     /// Get the error in ppm for this match, if it is a (partial) local match it will only take the matched amino acids into account.
     /// If there are multiple possible masses for any of the stretches it returns the smallest difference.
-    #[allow(clippy::missing_panics_doc)]
+    #[expect(clippy::missing_panics_doc)]
     pub fn ppm(&self) -> Ratio {
         self.mass_a()
             .iter()
@@ -580,7 +580,7 @@ impl Stats {
 }
 
 /// The score of an alignment
-#[derive(Clone, Copy, PartialEq, Eq, Hash, Debug, Serialize, Deserialize)]
+#[derive(Clone, Copy, Ord, PartialOrd, PartialEq, Eq, Hash, Debug, Serialize, Deserialize)]
 pub struct Score {
     /// The normalised score (absolute / max)
     pub normalised: OrderedFloat<f64>,
@@ -592,31 +592,31 @@ pub struct Score {
 }
 
 #[cfg(test)]
-#[allow(clippy::missing_panics_doc)]
+#[expect(clippy::missing_panics_doc)]
 mod tests {
     use crate::{
         align::{align, AlignScoring, AlignType},
-        peptide::SimpleLinear,
-        AminoAcid, LinearPeptide, MultiChemical,
+        peptidoform::SimpleLinear,
+        AminoAcid, MultiChemical, Peptidoform,
     };
 
     #[test]
     fn mass_difference() {
         // Test if the mass difference calculation is correct for some harder alignments.
         // A has an ambiguous AA, B and C have the two options, while D has a sub peptide of A.
-        let a = LinearPeptide::pro_forma("AABAA", None)
+        let a = Peptidoform::pro_forma("AABAA", None)
             .unwrap()
             .into_simple_linear()
             .unwrap();
-        let b = LinearPeptide::pro_forma("AANAA", None)
+        let b = Peptidoform::pro_forma("AANAA", None)
             .unwrap()
             .into_simple_linear()
             .unwrap();
-        let c = LinearPeptide::pro_forma("AADAA", None)
+        let c = Peptidoform::pro_forma("AADAA", None)
             .unwrap()
             .into_simple_linear()
             .unwrap();
-        let d = LinearPeptide::pro_forma("ADA", None)
+        let d = Peptidoform::pro_forma("ADA", None)
             .unwrap()
             .into_simple_linear()
             .unwrap();
diff --git a/rustyms/src/align/bad_alignments.rs b/rustyms/src/align/bad_alignments.rs
index 08c8b248..8d3528a2 100644
--- a/rustyms/src/align/bad_alignments.rs
+++ b/rustyms/src/align/bad_alignments.rs
@@ -2,7 +2,7 @@
 
 use crate::{
     align::{align, AlignScoring, AlignType},
-    LinearPeptide, SimpleLinear,
+    Peptidoform, SimpleLinear,
 };
 
 #[test]
@@ -11,11 +11,11 @@ fn overextended_rotation() {
 }
 
 fn test_alignment(peptide_one: &str, peptide_two: &str, path: &str) {
-    let first_peptide = LinearPeptide::pro_forma(peptide_one, None)
+    let first_peptide = Peptidoform::pro_forma(peptide_one, None)
         .unwrap()
         .into_simple_linear()
         .unwrap();
-    let second_peptide = LinearPeptide::pro_forma(peptide_two, None)
+    let second_peptide = Peptidoform::pro_forma(peptide_two, None)
         .unwrap()
         .into_simple_linear()
         .unwrap();
diff --git a/rustyms/src/align/consecutive.rs b/rustyms/src/align/consecutive.rs
index 03d93ef1..2d1b6bcb 100644
--- a/rustyms/src/align/consecutive.rs
+++ b/rustyms/src/align/consecutive.rs
@@ -2,7 +2,7 @@ use crate::{
     align::AlignScoring,
     align::*,
     imgt::*,
-    peptide::{AnnotatedPeptide, AtMax, Region, SimpleLinear, UnAmbiguous},
+    peptidoform::{AnnotatedPeptide, AtMax, Region, SimpleLinear, UnAmbiguous},
     *,
 };
 use std::collections::HashSet;
@@ -25,10 +25,10 @@ impl<'lifetime, A> ConsecutiveAlignment<'lifetime, A> {
     }
 }
 
-impl<'lifetime, A: AtMax<Linear>> ConsecutiveAlignment<'lifetime, A> {
+impl<A: AtMax<Linear>> ConsecutiveAlignment<'_, A> {
     /// Break up in the main alignment into the regions as annotated in the alleles.
-    #[allow(clippy::missing_panics_doc)]
-    pub fn regions(&self) -> Vec<(LinearPeptide<A>, Region)> {
+    #[expect(clippy::missing_panics_doc)]
+    pub fn regions(&self) -> Vec<(Peptidoform<A>, Region)> {
         let mut b_offset = 0;
         self.alignments
             .iter()
@@ -82,9 +82,9 @@ impl<'lifetime, A: AtMax<Linear>> ConsecutiveAlignment<'lifetime, A> {
 /// If the sequence is too short to cover all genes only the genes that could be matched are returned.
 /// # Panics
 /// If there are not two or more genes listed. If the return number is 0.
-#[allow(clippy::needless_pass_by_value)]
+#[expect(clippy::needless_pass_by_value)]
 pub fn consecutive_align<const STEPS: u16, A: AtMax<SimpleLinear> + AtMax<Linear>>(
-    sequence: &LinearPeptide<A>,
+    sequence: &Peptidoform<A>,
     genes: &[(GeneType, AlignType)],
     species: Option<HashSet<Species, impl std::hash::BuildHasher + Clone + Send + Sync + Default>>,
     chains: Option<HashSet<ChainType, impl std::hash::BuildHasher + Clone + Send + Sync + Default>>,
@@ -144,12 +144,12 @@ pub fn consecutive_align<const STEPS: u16, A: AtMax<SimpleLinear> + AtMax<Linear
 /// # Panics
 /// If there are not two or more genes listed. If the return number is 0.
 #[cfg(feature = "rayon")]
-#[allow(clippy::needless_pass_by_value)]
+#[expect(clippy::needless_pass_by_value)]
 pub fn par_consecutive_align<
     const STEPS: u16,
     A: AtMax<SimpleLinear> + AtMax<Linear> + Send + Sync,
 >(
-    sequence: &LinearPeptide<A>,
+    sequence: &Peptidoform<A>,
     genes: &[(GeneType, AlignType)],
     species: Option<HashSet<Species, impl std::hash::BuildHasher + Clone + Send + Sync + Default>>,
     chains: Option<HashSet<ChainType, impl std::hash::BuildHasher + Clone + Send + Sync + Default>>,
diff --git a/rustyms/src/align/diagonal_array.rs b/rustyms/src/align/diagonal_array.rs
index 76f18395..2afeef83 100644
--- a/rustyms/src/align/diagonal_array.rs
+++ b/rustyms/src/align/diagonal_array.rs
@@ -45,7 +45,7 @@ impl<T> DiagonalArray<T> {
     /// # Safety
     /// This function assumes the index to be valid. Not upholding this does an out of bounds unsafe [`[T]::get_unchecked_mut`].
     /// A debug assertion hold up this promise on debug builds.
-    #[allow(dead_code)]
+    #[expect(dead_code)]
     pub unsafe fn get_unchecked_mut(&mut self, index: [usize; 2]) -> &mut T {
         debug_assert!(self.validate_indices(index));
         let index = Self::length(index[0], self.max_depth) + index[1];
@@ -84,7 +84,7 @@ impl<T> std::ops::IndexMut<[usize; 2]> for DiagonalArray<T> {
 }
 
 #[cfg(test)]
-#[allow(clippy::missing_panics_doc)]
+#[expect(clippy::missing_panics_doc)]
 mod tests {
     use super::DiagonalArray;
 
diff --git a/rustyms/src/align/mass_alignment.rs b/rustyms/src/align/mass_alignment.rs
index de285273..a748a316 100644
--- a/rustyms/src/align/mass_alignment.rs
+++ b/rustyms/src/align/mass_alignment.rs
@@ -1,9 +1,9 @@
 use std::fmt::Debug;
 
 use crate::{
-    peptide::{AtMax, SimpleLinear},
+    peptidoform::{AtMax, SimpleLinear},
     system::Mass,
-    LinearPeptide, MassMode, MolecularFormula, Multi, SequenceElement, SequencePosition,
+    MassMode, MolecularFormula, Multi, Peptidoform, SequenceElement, SequencePosition,
     WithinTolerance,
 };
 
@@ -19,10 +19,10 @@ use super::{
 /// The [`AlignType`] controls the alignment behaviour, global/local or anything in between.
 /// # Panics
 /// It panics when the length of `seq_a` or `seq_b` is bigger than [`isize::MAX`].
-#[allow(clippy::too_many_lines)]
+#[expect(clippy::too_many_lines)]
 pub fn align<'lifetime, const STEPS: u16, A: AtMax<SimpleLinear>, B: AtMax<SimpleLinear>>(
-    seq_a: &'lifetime LinearPeptide<A>,
-    seq_b: &'lifetime LinearPeptide<B>,
+    seq_a: &'lifetime Peptidoform<A>,
+    seq_b: &'lifetime Peptidoform<B>,
     scoring: AlignScoring<'lifetime>,
     align_type: AlignType,
 ) -> Alignment<'lifetime, A, B> {
@@ -166,8 +166,8 @@ pub fn align<'lifetime, const STEPS: u16, A: AtMax<SimpleLinear>, B: AtMax<Simpl
 }
 
 pub(super) fn determine_final_score<A, B>(
-    seq_a: &LinearPeptide<A>,
-    seq_b: &LinearPeptide<B>,
+    seq_a: &Peptidoform<A>,
+    seq_b: &Peptidoform<B>,
     start_a: usize,
     start_b: usize,
     path: &[Piece],
@@ -256,14 +256,14 @@ fn score<A: AtMax<SimpleLinear>, B: AtMax<SimpleLinear>>(
                         .iter()
                         .enumerate()
                         .position(|(index, used)| !used && b.0[index] == *el)
-                        .map_or(false, |pos| {
+                        .is_some_and(|pos| {
                             b_copy[pos] = true;
                             true
                         })
                 })
             }
         };
-        #[allow(clippy::cast_possible_wrap)]
+        #[expect(clippy::cast_possible_wrap)]
         let local = scoring.mass_base as isize
             + if rotated {
                 scoring.rotated as isize * a.0.len() as isize
@@ -288,7 +288,7 @@ fn score<A: AtMax<SimpleLinear>, B: AtMax<SimpleLinear>>(
 
 /// Get the masses of all sequence elements
 fn calculate_masses<const STEPS: u16>(
-    sequence: &LinearPeptide<impl AtMax<SimpleLinear>>,
+    sequence: &Peptidoform<impl AtMax<SimpleLinear>>,
     mass_mode: MassMode,
 ) -> DiagonalArray<Multi<Mass>> {
     let mut array = DiagonalArray::new(sequence.len(), STEPS);
@@ -361,7 +361,7 @@ impl Matrix {
         }
     }
 
-    #[allow(clippy::cast_possible_wrap)]
+    #[expect(clippy::cast_possible_wrap)]
     pub fn global_start(&mut self, is_a: bool, scoring: AlignScoring<'_>) {
         let max = if is_a { self.a } else { self.b };
         for index in 0..=max {
@@ -480,7 +480,7 @@ impl std::ops::IndexMut<[usize; 2]> for Matrix {
 }
 
 #[cfg(test)]
-#[allow(clippy::missing_panics_doc)]
+#[expect(clippy::missing_panics_doc)]
 mod tests {
     use super::score;
     use crate::align::scoring::AlignScoring;
diff --git a/rustyms/src/align/mod.rs b/rustyms/src/align/mod.rs
index 033254bb..29ecd96e 100644
--- a/rustyms/src/align/mod.rs
+++ b/rustyms/src/align/mod.rs
@@ -18,8 +18,8 @@
 //! _Generated using this algorithm bound to a cli tool: <https://github.com/snijderlab/align-cli>_
 //! ```rust
 //! use rustyms::{*, align::*};
-//! let a = LinearPeptide::pro_forma("ANA", None).unwrap().into_simple_linear().unwrap();
-//! let b = LinearPeptide::pro_forma("AGGA", None).unwrap().into_simple_linear().unwrap();
+//! let a = Peptidoform::pro_forma("ANA", None).unwrap().into_simple_linear().unwrap();
+//! let b = Peptidoform::pro_forma("AGGA", None).unwrap().into_simple_linear().unwrap();
 //! let alignment = align::<4, SimpleLinear, SimpleLinear>(&a, &b, AlignScoring::default(), AlignType::GLOBAL);
 //! assert_eq!(alignment.short(), "1=1:2i1=");
 //! assert_eq!(alignment.ppm().value, 0.0);
@@ -31,6 +31,7 @@ mod alignment;
 mod bad_alignments;
 mod diagonal_array;
 mod mass_alignment;
+mod multi_alignment;
 mod piece;
 mod scoring;
 #[cfg(test)]
@@ -57,15 +58,15 @@ pub mod matrix {
 }
 
 #[cfg(test)]
-#[allow(clippy::missing_panics_doc)]
+#[expect(clippy::missing_panics_doc)]
 mod tests {
-    use crate::{peptide::SimpleLinear, LinearPeptide};
+    use crate::{peptidoform::SimpleLinear, Peptidoform};
 
     use super::{scoring::AlignScoring, AlignType, Alignment};
 
     fn align<'a, const STEPS: u16>(
-        a: &'a LinearPeptide<SimpleLinear>,
-        b: &'a LinearPeptide<SimpleLinear>,
+        a: &'a Peptidoform<SimpleLinear>,
+        b: &'a Peptidoform<SimpleLinear>,
     ) -> Alignment<'a, SimpleLinear, SimpleLinear> {
         super::align::<STEPS, SimpleLinear, SimpleLinear>(
             a,
@@ -75,8 +76,8 @@ mod tests {
         )
     }
 
-    fn linear(aa: &str) -> LinearPeptide<SimpleLinear> {
-        LinearPeptide::pro_forma(aa, None)
+    fn linear(aa: &str) -> Peptidoform<SimpleLinear> {
+        Peptidoform::pro_forma(aa, None)
             .unwrap()
             .into_simple_linear()
             .unwrap()
diff --git a/rustyms/src/align/multi_alignment.rs b/rustyms/src/align/multi_alignment.rs
new file mode 100644
index 00000000..24e72a8f
--- /dev/null
+++ b/rustyms/src/align/multi_alignment.rs
@@ -0,0 +1,45 @@
+#![allow(dead_code)]
+use std::borrow::Cow;
+
+use crate::Peptidoform;
+
+use super::{AlignType, MatchType, Score};
+
+use serde::{Deserialize, Serialize};
+
+type MultiAlignment<'lifetime, Complexity> = Vec<MultiAlignmentLine<'lifetime, Complexity>>;
+
+#[derive(Clone, Eq, PartialEq, Ord, PartialOrd, Hash, Debug, Serialize, Deserialize)]
+struct MultiAlignmentLine<'lifetime, Complexity> {
+    sequence: Cow<'lifetime, Peptidoform<Complexity>>,
+    path: Vec<MultiPiece>,
+    score: Score,
+    start: usize,
+    align_type: AlignType,
+    maximal_step: u16,
+}
+
+#[derive(Clone, Eq, PartialEq, Ord, PartialOrd, Hash, Debug, Default, Serialize, Deserialize)]
+struct MultiPiece {
+    score: isize,
+    local_score: isize,
+    match_type: MatchType,
+    step: u16,
+}
+
+impl<Complexity> MultiAlignmentLine<'_, Complexity> {
+    fn debug_display(&self) {
+        for piece in self
+            .path
+            .iter()
+            .zip(self.sequence.sequence().iter().skip(self.start))
+        {
+            print!(
+                "{}{}",
+                piece.1.aminoacid.char(),
+                "·".repeat(piece.0.step as usize - 1)
+            );
+        }
+        println!();
+    }
+}
diff --git a/rustyms/src/align/test_alignments.rs b/rustyms/src/align/test_alignments.rs
index 1a230199..8a3bc298 100644
--- a/rustyms/src/align/test_alignments.rs
+++ b/rustyms/src/align/test_alignments.rs
@@ -2,7 +2,7 @@
 
 use crate::{
     align::{align, scoring::AlignScoring, AlignType, Alignment},
-    LinearPeptide, SimpleLinear,
+    Peptidoform, SimpleLinear,
 };
 
 #[test]
@@ -162,11 +162,11 @@ fn test_alignment(
     path: &str,
 ) {
     const MAXIMAL_STEP: u16 = 4;
-    let first_peptide = LinearPeptide::pro_forma(seq_a, None)
+    let first_peptide = Peptidoform::pro_forma(seq_a, None)
         .unwrap()
         .into_simple_linear()
         .unwrap();
-    let second_peptide = LinearPeptide::pro_forma(seq_b, None)
+    let second_peptide = Peptidoform::pro_forma(seq_b, None)
         .unwrap()
         .into_simple_linear()
         .unwrap();
diff --git a/rustyms/src/aminoacids.rs b/rustyms/src/aminoacids.rs
index bdcaab77..687ec960 100644
--- a/rustyms/src/aminoacids.rs
+++ b/rustyms/src/aminoacids.rs
@@ -5,9 +5,62 @@ use crate::{
     fragment::{Fragment, FragmentType, PeptidePosition},
     model::*,
     molecular_charge::CachedCharge,
-    Multi, MultiChemical, NeutralLoss, SequencePosition,
+    system::Mass,
+    MassMode, Multi, MultiChemical, NeutralLoss, SequencePosition,
 };
 
+use std::borrow::Cow;
+
+/// A general trait to define amino acids.
+pub trait IsAminoAcid {
+    /// The full name for this amino acid.
+    fn name(&self) -> Cow<'_, str>;
+    /// The three letter code for this amino acid. Or None if there is no common three letter
+    /// definition for this amino acid.
+    fn three_letter_code(&self) -> Option<Cow<'_, str>>;
+    /// The one letter code for this amino acid. Or None if there is no common single character
+    /// definition for this amino acid.
+    #[doc(alias = "code")]
+    fn one_letter_code(&self) -> Option<char>;
+    /// The ProForma definition for this amino acid. If this is not a simple amino acid it can be
+    /// defined as an amino acid with an additional modification. For example `X[H9C2N2]` could be
+    /// used if Arginine was not defined as `R` in ProForma.
+    fn pro_forma_definition(&self) -> Cow<'_, str>;
+    /// The full molecular formula for this amino acid. It allows multiple molecular formulas to
+    /// allow ambiguous amino acids such as B and Z.
+    fn formulas(&self) -> Cow<'_, Multi<MolecularFormula>>;
+    /// The monoisotopic mass of this amino acid. Should be redefined for better performance.
+    fn monoisotopic_mass(&self) -> Cow<'_, Multi<Mass>> {
+        Cow::Owned(
+            self.formulas()
+                .iter()
+                .map(MolecularFormula::monoisotopic_mass)
+                .collect(),
+        )
+    }
+    /// The average weight of this amino acid. Should be redefined for better performance.
+    fn average_weight(&self) -> Cow<'_, Multi<Mass>> {
+        Cow::Owned(
+            self.formulas()
+                .iter()
+                .map(MolecularFormula::average_weight)
+                .collect(),
+        )
+    }
+    /// The mass with a given mass mode for this amino acid. Should be redefined for better performance.
+    fn mass(&self, mode: MassMode) -> Cow<'_, Multi<Mass>> {
+        Cow::Owned(self.formulas().iter().map(|f| f.mass(mode)).collect())
+    }
+    /// The molecular formula of the side chain of the amino acid.
+    fn side_chain(&self) -> Cow<'_, Multi<MolecularFormula>>;
+    /// The molecular formulas that can fragment for satellite ions (d and w). Commonly the fragment
+    /// after the second carbon into the side chain. `MolecularFormula::default()` can be returned
+    /// if no satellite ions are possible.
+    fn satellite_ion_fragments(&self) -> Option<Cow<'_, Multi<MolecularFormula>>>;
+    /// Common neutral losses for the immonium ion of this amino acid.
+    fn immonium_losses(&self) -> Cow<'_, [NeutralLoss]>;
+}
+
 include!("shared/aminoacid.rs");
 
 impl AminoAcid {
@@ -66,7 +119,7 @@ impl AminoAcid {
     pub(crate) fn satellite_ion_fragments(
         self,
         sequence_index: SequencePosition,
-        peptide_index: usize,
+        peptidoform_index: usize,
     ) -> Multi<MolecularFormula> {
         let crate::SequencePosition::Index(sequence_index) = sequence_index else {
             panic!("Not allowed to call satellite ion fragments with a terminal sequence index")
@@ -84,16 +137,16 @@ impl AminoAcid {
             Self::Asparagine => molecular_formula!(H 2 C 1 N 1 O 1).into(),
             Self::AsparticAcid => molecular_formula!(H 1 C 1 O 2).into(),
             Self::AmbiguousAsparagine => vec![
-                molecular_formula!(H 2 C 1 N 1 O 1 (crate::AmbiguousLabel::AminoAcid{option: Self::Asparagine, sequence_index, peptide_index})),
-                molecular_formula!(H 1 C 1 O 2 (crate::AmbiguousLabel::AminoAcid{option: Self::AsparticAcid, sequence_index, peptide_index})),
+                molecular_formula!(H 2 C 1 N 1 O 1 (crate::AmbiguousLabel::AminoAcid{option: Self::Asparagine, sequence_index, peptidoform_index})),
+                molecular_formula!(H 1 C 1 O 2 (crate::AmbiguousLabel::AminoAcid{option: Self::AsparticAcid, sequence_index, peptidoform_index})),
             ]
             .into(),
             Self::Cysteine => molecular_formula!(H 1 S 1).into(),
             Self::Glutamine => molecular_formula!(H 4 C 2 N 1 O 1).into(),
             Self::GlutamicAcid => molecular_formula!(H 3 C 2 O 2).into(),
             Self::AmbiguousGlutamine => vec![
-                molecular_formula!(H 4 C 2 N 1 O 1 (crate::AmbiguousLabel::AminoAcid{option: Self::Glutamine, sequence_index, peptide_index})),
-                molecular_formula!(H 3 C 2 O 2 (crate::AmbiguousLabel::AminoAcid{option: Self::GlutamicAcid, sequence_index, peptide_index})),
+                molecular_formula!(H 4 C 2 N 1 O 1 (crate::AmbiguousLabel::AminoAcid{option: Self::Glutamine, sequence_index, peptidoform_index})),
+                molecular_formula!(H 3 C 2 O 2 (crate::AmbiguousLabel::AminoAcid{option: Self::GlutamicAcid, sequence_index, peptidoform_index})),
             ]
             .into(),
             Self::Isoleucine => vec![
@@ -103,9 +156,9 @@ impl AminoAcid {
             .into(),
             Self::Leucine => molecular_formula!(H 7 C 3).into(),
             Self::AmbiguousLeucine => vec![
-                molecular_formula!(H 3 C 1 (crate::AmbiguousLabel::AminoAcid{option: Self::Isoleucine, sequence_index, peptide_index})),
-                molecular_formula!(H 5 C 2 (crate::AmbiguousLabel::AminoAcid{option: Self::Isoleucine, sequence_index, peptide_index})),
-                molecular_formula!(H 7 C 3 (crate::AmbiguousLabel::AminoAcid{option: Self::Leucine, sequence_index, peptide_index})),
+                molecular_formula!(H 3 C 1 (crate::AmbiguousLabel::AminoAcid{option: Self::Isoleucine, sequence_index, peptidoform_index})),
+                molecular_formula!(H 5 C 2 (crate::AmbiguousLabel::AminoAcid{option: Self::Isoleucine, sequence_index, peptidoform_index})),
+                molecular_formula!(H 7 C 3 (crate::AmbiguousLabel::AminoAcid{option: Self::Leucine, sequence_index, peptidoform_index})),
             ]
             .into(),
             Self::Lysine => molecular_formula!(H 8 C 3 N 1).into(),
@@ -124,7 +177,7 @@ impl AminoAcid {
 
     /// All losses from the base immonium ions. Compiled from the sources below.
     ///
-    /// | AA  | [Wikipedia](https://upload.wikimedia.org/wikipedia/commons/thumb/0/01/Amino_acid_fragment_ions.png/400px-Amino_acid_fragment_ions.png) |  0.1016/1044-0305(93)87006-X  | [ionsource](https://www.ionsource.com/Card/immon/immon.htm) | [10.1002/chin.199624319](http://dx.doi.org/10.1002/chin.199624319) | [Prospector   (MS-Comp)](https://prospector.ucsf.edu/prospector/cgi-bin/msform.cgi?form=mscomp) | [10.1186/1477-5956-9-2](http://dx.doi.org/10.1186/1477-5956-9-2) |  10.1016/j.ymeth.2004.08.013   | 10.1385/1597452750 (table 5)  | 10.1021/ac902712f  | [Prospector   (MS-Product)](https://prospector.ucsf.edu/prospector/cgi-bin/msform.cgi?form=msproduct) | [ThermoFisher](https://tools.thermofisher.com/content/sfs/brochures/cms_040030.pdf) | 10.1074/mcp.O113.035915 | 10.1074/mcp.O113.035915 | 10.1021/ac902712f | [Prospector   (MS-Product)](https://prospector.ucsf.edu/prospector/cgi-bin/msform.cgi?form=msproduct) |  | 10.1385/1597452750 (table 5) | Sources | Best mass | Best formula | Loss     | Loss formula | Interpreted loss | Interpreted formula     | Final      |
+    /// | AA    | [Wikipedia](https://upload.wikimedia.org/wikipedia/commons/thumb/0/01/Amino_acid_fragment_ions.png/400px-Amino_acid_fragment_ions.png) |  0.1016/1044-0305(93)87006-X  | [ionsource](https://www.ionsource.com/Card/immon/immon.htm) | [10.1002/chin.199624319](http://dx.doi.org/10.1002/chin.199624319) | [Prospector   (MS-Comp)](https://prospector.ucsf.edu/prospector/cgi-bin/msform.cgi?form=mscomp) | [10.1186/1477-5956-9-2](http://dx.doi.org/10.1186/1477-5956-9-2) |  10.1016/j.ymeth.2004.08.013   | 10.1385/1597452750 (table 5)  | 10.1021/ac902712f  | [Prospector   (MS-Product)](https://prospector.ucsf.edu/prospector/cgi-bin/msform.cgi?form=msproduct) | [ThermoFisher](https://tools.thermofisher.com/content/sfs/brochures/cms_040030.pdf) | 10.1074/mcp.O113.035915 | 10.1074/mcp.O113.035915 | 10.1021/ac902712f | [Prospector   (MS-Product)](https://prospector.ucsf.edu/prospector/cgi-bin/msform.cgi?form=msproduct) |  | 10.1385/1597452750 (table 5) | Sources | Best mass | Best formula | Loss     | Loss formula | Interpreted loss | Interpreted formula     | Final      |
     /// |-------|---------------------------------------------------------------------------------------------------------------------------|-----------------------------|------------------------------------------------|------------------------------------------|-----------------------------------------------------------------------|-----------------------------------------|-----------------------------|------------------------------|-------------------|--------------------------------------------------------------------------|---------------------------------------------------------------------|-------------------------|-------------------------|-------------------|--------------------------------------------------------------------------|------------------------------|---------|----------:|--------------|----------|--------------|------------------|-------------------------|------------|
     /// | A     | 44                                                                                                                        | 44                          |                                                | 44                                       |                                                                       | 44                                      |                             | 44.05                        |                   |                                                                          | 44.0500                                                             |                         |                         |                   |                                                                          |                              | 6       |   44.0500 |              |          |              |                  |                         |            |
     /// | R     | 129                                                                                                                       | 129                         |                                                | 129                                      |                                                                       | 129                                     |                             | 129.11                       |                   |                                                                          | 129.1140                                                            | 129.1135                | C5H13N4+                |                   |                                                                          |                              | 8       |  129.1138 | C5H13N4+     |          |              |                  |                         |            |
@@ -271,7 +324,8 @@ impl AminoAcid {
         }
     }
 
-    #[allow(clippy::too_many_lines, clippy::too_many_arguments)]
+    // TODO: generalise over used storage type, so using molecularformula, monoisotopic mass, or average mass, also make sure that AAs can return these numbers in a const fashion
+    #[expect(clippy::too_many_lines, clippy::too_many_arguments)]
     pub(crate) fn fragments(
         self,
         n_term: &Multi<MolecularFormula>,
@@ -281,8 +335,8 @@ impl AminoAcid {
         sequence_index: SequencePosition,
         sequence_length: usize,
         ions: &PossibleIons,
+        peptidoform_ion_index: usize,
         peptidoform_index: usize,
-        peptide_index: usize,
         allow_terminal: (bool, bool),
     ) -> Vec<Fragment> {
         let mut base_fragments = Vec::with_capacity(ions.size_upper_bound());
@@ -291,10 +345,10 @@ impl AminoAcid {
 
         if ions.a.0 && allow_terminal.0 {
             base_fragments.extend(Fragment::generate_all(
-                &(self.formulas_inner(sequence_index, peptide_index)
+                &(self.formulas_inner(sequence_index, peptidoform_index)
                     * (modifications - molecular_formula!(H 1 C 1 O 1))),
+                peptidoform_ion_index,
                 peptidoform_index,
-                peptide_index,
                 &FragmentType::a(n_pos),
                 n_term,
                 ions.a.1,
@@ -304,10 +358,10 @@ impl AminoAcid {
         }
         if ions.b.0 && allow_terminal.0 {
             base_fragments.extend(Fragment::generate_all(
-                &(self.formulas_inner(sequence_index, peptide_index)
+                &(self.formulas_inner(sequence_index, peptidoform_index)
                     * (modifications - molecular_formula!(H 1))),
+                peptidoform_ion_index,
                 peptidoform_index,
-                peptide_index,
                 &FragmentType::b(n_pos),
                 n_term,
                 ions.b.1,
@@ -317,10 +371,10 @@ impl AminoAcid {
         }
         if ions.c.0 && allow_terminal.0 {
             base_fragments.extend(Fragment::generate_all(
-                &(self.formulas_inner(sequence_index, peptide_index)
+                &(self.formulas_inner(sequence_index, peptidoform_index)
                     * (modifications + molecular_formula!(H 2 N 1))),
+                peptidoform_ion_index,
                 peptidoform_index,
-                peptide_index,
                 &FragmentType::c(n_pos),
                 n_term,
                 ions.c.1,
@@ -330,12 +384,12 @@ impl AminoAcid {
         }
         if ions.d.0 && allow_terminal.0 {
             base_fragments.extend(Fragment::generate_all(
-                &(-self.satellite_ion_fragments(sequence_index, peptide_index)
+                &(-self.satellite_ion_fragments(sequence_index, peptidoform_index)
                     * modifications
-                    * self.formulas_inner(sequence_index, peptide_index)
+                    * self.formulas_inner(sequence_index, peptidoform_index)
                     + molecular_formula!(H 1 C 1 O 1)),
+                peptidoform_ion_index,
                 peptidoform_index,
-                peptide_index,
                 &FragmentType::d(n_pos),
                 n_term,
                 ions.d.1,
@@ -346,8 +400,8 @@ impl AminoAcid {
         if ions.v.0 && allow_terminal.1 {
             base_fragments.extend(Fragment::generate_all(
                 &molecular_formula!(H 3 C 2 N 1 O 1).into(),
+                peptidoform_ion_index,
                 peptidoform_index,
-                peptide_index,
                 &FragmentType::v(c_pos),
                 c_term,
                 ions.v.1,
@@ -357,12 +411,12 @@ impl AminoAcid {
         }
         if ions.w.0 && allow_terminal.1 {
             base_fragments.extend(Fragment::generate_all(
-                &(-self.satellite_ion_fragments(sequence_index, peptide_index)
+                &(-self.satellite_ion_fragments(sequence_index, peptidoform_index)
                     * modifications
-                    * self.formulas_inner(sequence_index, peptide_index)
+                    * self.formulas_inner(sequence_index, peptidoform_index)
                     + molecular_formula!(H 2 N 1)),
+                peptidoform_ion_index,
                 peptidoform_index,
-                peptide_index,
                 &FragmentType::w(c_pos),
                 c_term,
                 ions.w.1,
@@ -372,10 +426,10 @@ impl AminoAcid {
         }
         if ions.x.0 && allow_terminal.1 {
             base_fragments.extend(Fragment::generate_all(
-                &(self.formulas_inner(sequence_index, peptide_index)
+                &(self.formulas_inner(sequence_index, peptidoform_index)
                     * (modifications + molecular_formula!(C 1 O 1) - molecular_formula!(H 1))),
+                peptidoform_ion_index,
                 peptidoform_index,
-                peptide_index,
                 &FragmentType::x(c_pos),
                 c_term,
                 ions.x.1,
@@ -385,10 +439,10 @@ impl AminoAcid {
         }
         if ions.y.0 && allow_terminal.1 {
             base_fragments.extend(Fragment::generate_all(
-                &(self.formulas_inner(sequence_index, peptide_index)
+                &(self.formulas_inner(sequence_index, peptidoform_index)
                     * (modifications + molecular_formula!(H 1))),
+                peptidoform_ion_index,
                 peptidoform_index,
-                peptide_index,
                 &FragmentType::y(c_pos),
                 c_term,
                 ions.y.1,
@@ -398,10 +452,10 @@ impl AminoAcid {
         }
         if ions.z.0 && allow_terminal.1 {
             base_fragments.extend(Fragment::generate_all(
-                &(self.formulas_inner(sequence_index, peptide_index)
+                &(self.formulas_inner(sequence_index, peptidoform_index)
                     * (modifications - molecular_formula!(H 2 N 1))),
+                peptidoform_ion_index,
                 peptidoform_index,
-                peptide_index,
                 &FragmentType::z(c_pos),
                 c_term,
                 ions.z.1,
@@ -409,10 +463,10 @@ impl AminoAcid {
                 ions.z.2,
             ));
             base_fragments.extend(Fragment::generate_all(
-                &(self.formulas_inner(sequence_index, peptide_index)
+                &(self.formulas_inner(sequence_index, peptidoform_index)
                     * (modifications - molecular_formula!(H 1 N 1))),
+                peptidoform_ion_index,
                 peptidoform_index,
-                peptide_index,
                 &FragmentType::z·(c_pos),
                 c_term,
                 ions.z.1,
@@ -423,10 +477,10 @@ impl AminoAcid {
 
         if ions.immonium.0 && allow_terminal.0 && allow_terminal.1 {
             base_fragments.extend(Fragment::generate_all(
-                &(self.formulas_inner(sequence_index, peptide_index)
+                &(self.formulas_inner(sequence_index, peptidoform_index)
                     * (modifications - molecular_formula!(C 1 O 1))),
+                peptidoform_ion_index,
                 peptidoform_index,
-                peptide_index,
                 &FragmentType::Immonium(n_pos, self.into()), // TODO: get the actual sequenceelement here
                 &Multi::default(),
                 self.immonium_losses().as_slice(),
@@ -557,11 +611,7 @@ impl std::fmt::Display for AminoAcid {
 }
 
 #[cfg(test)]
-#[allow(
-    clippy::unreadable_literal,
-    clippy::float_cmp,
-    clippy::missing_panics_doc
-)]
+#[expect(clippy::unreadable_literal, clippy::missing_panics_doc)]
 mod tests {
     use super::*;
 
diff --git a/rustyms/src/checked_aminoacid.rs b/rustyms/src/checked_aminoacid.rs
index 2ac61464..f709c828 100644
--- a/rustyms/src/checked_aminoacid.rs
+++ b/rustyms/src/checked_aminoacid.rs
@@ -18,7 +18,7 @@ pub struct CheckedAminoAcid<T> {
     marker: PhantomData<T>,
 }
 
-#[allow(non_upper_case_globals, missing_docs)]
+#[expect(non_upper_case_globals, missing_docs)]
 impl CheckedAminoAcid<UnAmbiguous> {
     pub const A: Self = Self::Alanine;
     pub const C: Self = Self::Cysteine;
@@ -215,7 +215,7 @@ impl CheckedAminoAcid<UnAmbiguous> {
     ];
 }
 
-#[allow(non_upper_case_globals, missing_docs)]
+#[expect(non_upper_case_globals, missing_docs)]
 impl CheckedAminoAcid<SemiAmbiguous> {
     pub const B: Self = Self::AmbiguousAsparagine;
     pub const Z: Self = Self::AmbiguousGlutamine;
@@ -305,7 +305,7 @@ impl Chemical for CheckedAminoAcid<UnAmbiguous> {
     fn formula_inner(
         &self,
         _sequence_index: crate::SequencePosition,
-        _peptide_index: usize,
+        _peptidoform_index: usize,
     ) -> MolecularFormula {
         match self.aminoacid {
             AminoAcid::Alanine => molecular_formula!(H 5 C 3 O 1 N 1),
@@ -343,7 +343,7 @@ impl<T> MultiChemical for CheckedAminoAcid<T> {
     fn formulas_inner(
         &self,
         sequence_index: crate::SequencePosition,
-        peptide_index: usize,
+        peptidoform_index: usize,
     ) -> Multi<MolecularFormula> {
         self.into_unambiguous().map_or_else(|| {
             let crate::SequencePosition::Index(sequence_index) = sequence_index else {
@@ -351,17 +351,17 @@ impl<T> MultiChemical for CheckedAminoAcid<T> {
             };
             match self.aminoacid {
             AminoAcid::AmbiguousAsparagine => vec![
-                molecular_formula!(H 6 C 4 O 2 N 2 (crate::AmbiguousLabel::AminoAcid{option: AminoAcid::Asparagine, sequence_index, peptide_index})),
-                molecular_formula!(H 5 C 4 O 3 N 1 (crate::AmbiguousLabel::AminoAcid{option: AminoAcid::AsparticAcid, sequence_index, peptide_index})),
+                molecular_formula!(H 6 C 4 O 2 N 2 (crate::AmbiguousLabel::AminoAcid{option: AminoAcid::Asparagine, sequence_index, peptidoform_index})),
+                molecular_formula!(H 5 C 4 O 3 N 1 (crate::AmbiguousLabel::AminoAcid{option: AminoAcid::AsparticAcid, sequence_index, peptidoform_index})),
             ]
             .into(),
             AminoAcid::AmbiguousGlutamine => vec![
-                molecular_formula!(H 8 C 5 O 2 N 2 (crate::AmbiguousLabel::AminoAcid{option: AminoAcid::Glutamine, sequence_index, peptide_index})),
-                molecular_formula!(H 7 C 5 O 3 N 1 (crate::AmbiguousLabel::AminoAcid{option: AminoAcid::GlutamicAcid, sequence_index, peptide_index})),
+                molecular_formula!(H 8 C 5 O 2 N 2 (crate::AmbiguousLabel::AminoAcid{option: AminoAcid::Glutamine, sequence_index, peptidoform_index})),
+                molecular_formula!(H 7 C 5 O 3 N 1 (crate::AmbiguousLabel::AminoAcid{option: AminoAcid::GlutamicAcid, sequence_index, peptidoform_index})),
             ]
             .into(),
             _ => unreachable!(),        }
-        }, |unambiguous| unambiguous.formula_inner(sequence_index, peptide_index).into())
+        }, |unambiguous| unambiguous.formula_inner(sequence_index, peptidoform_index).into())
     }
 }
 
diff --git a/rustyms/src/databases/gnome.dat b/rustyms/src/databases/gnome.dat
index 03aa9fb0..7ddd75b6 100644
Binary files a/rustyms/src/databases/gnome.dat and b/rustyms/src/databases/gnome.dat differ
diff --git a/rustyms/src/element.rs b/rustyms/src/element.rs
index 9d0304f5..015d8def 100644
--- a/rustyms/src/element.rs
+++ b/rustyms/src/element.rs
@@ -102,7 +102,7 @@ pub fn elemental_data() -> &'static ElementalData {
 static ELEMENTAL_DATA_CELL: OnceLock<ElementalData> = OnceLock::new();
 
 #[cfg(test)]
-#[allow(clippy::missing_panics_doc)]
+#[expect(clippy::missing_panics_doc)]
 mod test {
     #[test]
     fn hill_notation() {
diff --git a/rustyms/src/error/context.rs b/rustyms/src/error/context.rs
index e52e07a2..03447209 100644
--- a/rustyms/src/error/context.rs
+++ b/rustyms/src/error/context.rs
@@ -65,7 +65,7 @@ pub enum Context {
     },
 }
 
-#[allow(clippy::needless_pass_by_value, dead_code)] // the impl ToString should be passed like this, otherwise &str gives errors
+#[expect(clippy::needless_pass_by_value)] // the impl ToString should be passed like this, otherwise &str gives errors
 impl Context {
     /// Creates a new context when no context can be given
     pub const fn none() -> Self {
@@ -135,7 +135,7 @@ impl Context {
     }
 
     /// Creates a new context to highlight a certain position
-    #[allow(clippy::unwrap_used, clippy::missing_panics_doc)]
+    #[expect(clippy::unwrap_used, clippy::missing_panics_doc)]
     pub fn position(pos: &FilePosition<'_>) -> Self {
         if pos.text.is_empty() {
             Self::Line {
@@ -227,7 +227,7 @@ impl Context {
     fn display(&self, f: &mut fmt::Formatter<'_>, note: Option<&str>) -> fmt::Result {
         const MAX_COLS: usize = 95;
         let mut tail = true; // End with a tailing line ╵
-        #[allow(
+        #[expect(
             clippy::cast_sign_loss,
             clippy::cast_precision_loss,
             clippy::cast_possible_truncation
@@ -330,7 +330,7 @@ impl Context {
                 write!(f, "\n{:pad$} ╷", "", pad = margin)?;
                 let mut number = *start_linenumber + 1;
                 let mut highlights_peek = highlights.iter().peekable();
-                #[allow(unused)]
+
                 for (index, line) in lines.iter().enumerate() {
                     number += 1;
                     write!(f, "\n{number:<margin$} │ {line}")?;
diff --git a/rustyms/src/error/custom_error.rs b/rustyms/src/error/custom_error.rs
index 5a1b05ea..5dbd07de 100644
--- a/rustyms/src/error/custom_error.rs
+++ b/rustyms/src/error/custom_error.rs
@@ -5,7 +5,7 @@ use std::error;
 use std::fmt;
 
 /// An error. Stored as a pointer to a structure on the heap to prevent large sizes which could be
-/// detremental to performance for the happy path.
+/// detrimental to performance for the happy path.
 #[derive(Serialize, Deserialize, PartialEq, Clone, Eq, Hash)]
 pub struct CustomError {
     content: Box<InnerError>,
@@ -29,7 +29,7 @@ struct InnerError {
     underlying_errors: Vec<CustomError>,
 }
 
-#[allow(clippy::needless_pass_by_value, dead_code)] // The impl ToString should be passed like this, otherwise &str gives errors
+#[expect(clippy::needless_pass_by_value)] // The impl ToString should be passed like this, otherwise &str gives errors
 impl CustomError {
     /// Create a new `CustomError`.
     ///
@@ -233,7 +233,7 @@ impl fmt::Display for CustomError {
 impl error::Error for CustomError {}
 
 #[cfg(test)]
-#[allow(clippy::print_stdout, clippy::missing_panics_doc)]
+#[expect(clippy::print_stdout, clippy::missing_panics_doc)]
 mod tests {
     use super::*;
     use crate::error::FilePosition;
diff --git a/rustyms/src/error/mod.rs b/rustyms/src/error/mod.rs
index ac79fc5a..a6b5eebd 100644
--- a/rustyms/src/error/mod.rs
+++ b/rustyms/src/error/mod.rs
@@ -5,6 +5,5 @@ mod context;
 /// An error with all its properties
 mod custom_error;
 
-#[allow(unused_imports)]
 pub use context::{Context, FilePosition};
 pub use custom_error::CustomError;
diff --git a/rustyms/src/formula.rs b/rustyms/src/formula.rs
index f84ff98e..c85739f0 100644
--- a/rustyms/src/formula.rs
+++ b/rustyms/src/formula.rs
@@ -19,7 +19,7 @@ impl From<&MolecularFormula> for OrderedMass {
 
 impl MolecularFormula {
     /// The mass of the molecular formula of this element, if all element species (isotopes) exists
-    #[allow(clippy::missing_panics_doc)]
+    #[expect(clippy::missing_panics_doc)]
     pub fn monoisotopic_mass(&self) -> Mass {
         let mut mass = da(*self.additional_mass);
         for (e, i, n) in &self.elements {
@@ -32,7 +32,7 @@ impl MolecularFormula {
     }
 
     /// The average weight of the molecular formula of this element, if all element species (isotopes) exists
-    #[allow(clippy::missing_panics_doc)]
+    #[expect(clippy::missing_panics_doc)]
     pub fn average_weight(&self) -> Mass {
         let mut mass = da(*self.additional_mass); // Technically this is wrong, the additional mass is defined to be monoisotopic
         for (e, i, n) in &self.elements {
@@ -49,7 +49,6 @@ impl MolecularFormula {
     /// but will be in the form of monoisotopic exact mass + n, where n is the integer dalton offset for that isomer.
     ///
     /// Only available with crate feature 'isotopes'.
-    #[allow(clippy::missing_panics_doc)]
     #[cfg(feature = "isotopes")]
     pub fn most_abundant_mass(&self) -> Mass {
         let isotopes = self.isotopic_distribution(0.01);
@@ -130,13 +129,13 @@ impl std::fmt::Display for AmbiguousLabel {
             Self::AminoAcid {
                 option,
                 sequence_index,
-                peptide_index,
-            } => write!(f, "{option}@p{peptide_index}i{sequence_index}"),
+                peptidoform_index,
+            } => write!(f, "{option}@p{peptidoform_index}i{sequence_index}"),
             Self::Modification {
                 id,
                 sequence_index,
-                peptide_index,
-            } => write!(f, "\x23{id}@p{peptide_index}i{sequence_index}"),
+                peptidoform_index,
+            } => write!(f, "\x23{id}@p{peptidoform_index}i{sequence_index}"),
             Self::ChargeCarrier(formula) => write!(f, "[{}]", formula.hill_notation()),
             Self::CrossLinkBound(name) => write!(f, "intact{name}"),
             Self::CrossLinkBroken(name, formula) => {
@@ -146,7 +145,7 @@ impl std::fmt::Display for AmbiguousLabel {
     }
 }
 
-#[allow(clippy::missing_panics_doc)] // Cannot panic
+#[expect(clippy::missing_panics_doc)] // Cannot panic
 fn to_subscript_num(input: isize) -> String {
     let text = input.to_string();
     let mut output = String::new();
@@ -160,7 +159,7 @@ fn to_subscript_num(input: isize) -> String {
     output
 }
 
-#[allow(clippy::missing_panics_doc)] // Cannot panic
+#[expect(clippy::missing_panics_doc)] // Cannot panic
 fn to_superscript_num(input: u16) -> String {
     let text = input.to_string();
     let mut output = String::new();
@@ -186,7 +185,7 @@ impl std::fmt::Display for MolecularFormula {
 }
 
 #[cfg(test)]
-#[allow(clippy::missing_panics_doc)]
+#[expect(clippy::missing_panics_doc)]
 mod tests {
     use crate::{
         model::ChargeRange, molecular_formula, AminoAcid, Fragment, MolecularCharge,
@@ -292,7 +291,7 @@ mod tests {
     }
 
     #[test]
-    #[allow(clippy::similar_names)]
+    #[expect(clippy::similar_names)]
     fn labels() {
         let labelled = AminoAcid::AmbiguousAsparagine.formulas();
         let unlabelled: crate::Multi<MolecularFormula> =
diff --git a/rustyms/src/formula_search.rs b/rustyms/src/formula_search.rs
new file mode 100644
index 00000000..03dfce45
--- /dev/null
+++ b/rustyms/src/formula_search.rs
@@ -0,0 +1,53 @@
+use std::num::NonZeroU16;
+
+use crate::{system::Mass, Element, MolecularFormula, Multi, Tolerance};
+
+/// Find the isobaric sets for the given mass with the given modifications and ppm error.
+/// The modifications are placed on any location they are allowed based on the given placement
+/// rules, so using any modifications which provide those is advised. If the provided [`LinearPeptide`]
+/// has multiple formulas, it uses the formula with the lowest monoisotopic mass.
+/// # Panics
+/// Panics if any of the modifications does not have a defined mass. Or if the weight of the
+/// base selection is already in the tolerance of the given mass.
+pub fn find_formulas(
+    mass: Mass,
+    tolerance: Tolerance<Mass>,
+    elements: &[(Element, Option<NonZeroU16>)],
+) -> Multi<MolecularFormula> {
+    let bounds = tolerance.bounds(mass);
+    let mut options: Vec<(Mass, MolecularFormula)> = Vec::new();
+
+    for (element, isotope) in elements.iter().copied() {
+        if !element.is_valid(isotope) {
+            continue;
+        }
+        let mass = element.mass(isotope).unwrap();
+        let mut new_options = Vec::with_capacity(options.len());
+        if mass <= bounds.1 {
+            new_options.extend((1..=(bounds.1 / mass).value.floor() as i32).map(|n| {
+                (
+                    mass * f64::from(n),
+                    MolecularFormula::new(&[(element, isotope, n)], &[]).unwrap(),
+                )
+            }));
+        }
+        for option in &options {
+            let rest = bounds.1 - option.0;
+            if mass <= rest {
+                new_options.extend((1..=(rest / mass).value.floor() as i32).map(|n| {
+                    let mut new_formula = option.1.clone();
+                    let _ = new_formula.add((element, isotope, n));
+                    (option.0 + mass * f64::from(n), new_formula)
+                }));
+            }
+        }
+        options.extend_from_slice(&new_options);
+    }
+    options.sort_by(|a, b| a.0.value.total_cmp(&b.0.value));
+    options
+        .into_iter()
+        .skip_while(|(mass, _)| *mass < bounds.0)
+        .take_while(|(mass, _)| *mass < bounds.1)
+        .map(|(_, formula)| formula)
+        .collect()
+}
diff --git a/rustyms/src/fragment.rs b/rustyms/src/fragment.rs
index 06a0161b..b93b362e 100644
--- a/rustyms/src/fragment.rs
+++ b/rustyms/src/fragment.rs
@@ -32,9 +32,9 @@ pub struct Fragment {
     /// All possible annotations for this fragment saved as a tuple of peptide index and its type
     pub ion: FragmentType,
     /// The peptidoform this fragment comes from, saved as the index into the list of peptidoform in the overarching [`crate::CompoundPeptidoform`] struct
-    pub peptidoform_index: Option<usize>,
+    pub peptidoform_ion_index: Option<usize>,
     /// The peptide this fragment comes from, saved as the index into the list of peptides in the overarching [`crate::Peptidoform`] struct
-    pub peptide_index: Option<usize>,
+    pub peptidoform_index: Option<usize>,
     /// Any neutral losses applied
     pub neutral_loss: Vec<NeutralLoss>,
     /// m/z deviation, if known (from mzPAF)
@@ -68,16 +68,16 @@ impl Fragment {
     pub fn new(
         theoretical_mass: MolecularFormula,
         charge: Charge,
+        peptidoform_ion_index: usize,
         peptidoform_index: usize,
-        peptide_index: usize,
         ion: FragmentType,
     ) -> Self {
         Self {
             formula: Some(theoretical_mass),
             charge,
             ion,
+            peptidoform_ion_index: Some(peptidoform_ion_index),
             peptidoform_index: Some(peptidoform_index),
-            peptide_index: Some(peptide_index),
             neutral_loss: Vec::new(),
             deviation: None,
             confidence: None,
@@ -88,12 +88,12 @@ impl Fragment {
     /// Generate a list of possible fragments from the list of possible preceding termini and neutral losses
     /// # Panics
     /// When the charge range results in a negative charge
-    #[allow(clippy::too_many_arguments)]
+    #[expect(clippy::too_many_arguments)]
     #[must_use]
     pub fn generate_all(
         theoretical_mass: &Multi<MolecularFormula>,
+        peptidoform_ion_index: usize,
         peptidoform_index: usize,
-        peptide_index: usize,
         annotation: &FragmentType,
         termini: &Multi<MolecularFormula>,
         neutral_losses: &[NeutralLoss],
@@ -108,13 +108,13 @@ impl Fragment {
             .map(|(((term, mass), charge), loss)| Self {
                 formula: Some(
                     term + mass
-                        + charge.formula_inner(SequencePosition::default(), peptide_index)
+                        + charge.formula_inner(SequencePosition::default(), peptidoform_index)
                         + loss.unwrap_or(&NeutralLoss::Gain(MolecularFormula::default())),
                 ),
                 charge: Charge::new::<crate::system::e>(charge.charge().value.try_into().unwrap()),
                 ion: annotation.clone(),
+                peptidoform_ion_index: Some(peptidoform_ion_index),
                 peptidoform_index: Some(peptidoform_index),
-                peptide_index: Some(peptide_index),
                 neutral_loss: loss.map(|l| vec![l.clone()]).unwrap_or_default(),
                 deviation: None,
                 confidence: None,
@@ -335,7 +335,7 @@ pub enum DiagnosticPosition {
 
 /// The possible types of fragments
 #[derive(Clone, Eq, PartialEq, Ord, PartialOrd, Hash, Debug, Serialize, Deserialize, Default)]
-#[allow(non_camel_case_types)]
+#[expect(non_camel_case_types)]
 pub enum FragmentType {
     /// a
     a(PeptidePosition),
@@ -547,7 +547,7 @@ impl Display for FragmentType {
 
 /// The possible kinds of N terminal backbone fragments.
 #[derive(Copy, Clone, Eq, PartialEq, Ord, PartialOrd, Hash, Debug, Serialize, Deserialize)]
-#[allow(non_camel_case_types)]
+#[expect(non_camel_case_types)]
 pub enum BackboneNFragment {
     /// a
     a,
@@ -573,7 +573,7 @@ impl Display for BackboneNFragment {
 
 /// The possible kinds of C terminal backbone fragments.
 #[derive(Copy, Clone, Eq, PartialEq, Ord, PartialOrd, Hash, Debug, Serialize, Deserialize)]
-#[allow(non_camel_case_types)]
+#[expect(non_camel_case_types)]
 pub enum BackboneCFragment {
     /// x
     x,
@@ -599,7 +599,7 @@ impl Display for BackboneCFragment {
 
 /// The possible kinds of fragments, same options as [`FragmentType`] but without any additional data
 #[derive(Copy, Clone, Eq, PartialEq, Ord, PartialOrd, Hash, Debug, Serialize, Deserialize)]
-#[allow(non_camel_case_types)]
+#[expect(non_camel_case_types)]
 pub enum FragmentKind {
     /// a
     a,
@@ -701,7 +701,7 @@ impl std::fmt::Display for GlycanBreakPos {
 }
 
 #[cfg(test)]
-#[allow(clippy::missing_panics_doc)]
+#[expect(clippy::missing_panics_doc)]
 mod tests {
 
     use crate::{AminoAcid, MultiChemical};
diff --git a/rustyms/src/fragmentation_tests.rs b/rustyms/src/fragmentation_tests.rs
index f52a7fb7..af798037 100644
--- a/rustyms/src/fragmentation_tests.rs
+++ b/rustyms/src/fragmentation_tests.rs
@@ -18,7 +18,7 @@ use itertools::Itertools;
 #[test]
 fn triple_a() {
     // Compare rustyms with https://proteomicsresource.washington.edu/cgi-bin/fragment.cgi
-    #[allow(clippy::unreadable_literal)]
+    #[expect(clippy::unreadable_literal)]
     let theoretical_fragments = &[
         (44.049476, "a+1"),
         (72.044390, "b+1"),
@@ -45,7 +45,7 @@ fn triple_a() {
         .z(PrimaryIonSeries::default());
     test(
         theoretical_fragments,
-        LinearPeptide::pro_forma("AAA", None)
+        Peptidoform::pro_forma("AAA", None)
             .unwrap()
             .into_linear()
             .unwrap(),
@@ -59,7 +59,7 @@ fn triple_a() {
 #[test]
 fn with_modifications() {
     // Compare rustyms with https://proteomicsresource.washington.edu/cgi-bin/fragment.cgi mods: -17.02655@[ 15.99491@
-    #[allow(clippy::unreadable_literal)]
+    #[expect(clippy::unreadable_literal)]
     let theoretical_fragments = &[
         (84.044389, "a1"),
         (155.081503, "a2"),
@@ -93,7 +93,7 @@ fn with_modifications() {
         .z(PrimaryIonSeries::default());
     test(
         theoretical_fragments,
-        LinearPeptide::pro_forma("[Gln->pyro-Glu]-QAAM[Oxidation]", None).unwrap(),
+        Peptidoform::pro_forma("[Gln->pyro-Glu]-QAAM[Oxidation]", None).unwrap(),
         &model,
         1,
         true,
@@ -101,66 +101,66 @@ fn with_modifications() {
     );
 }
 
-#[test]
-fn with_possible_modifications() {
-    // Compare rustyms with https://proteomicsresource.washington.edu/cgi-bin/fragment.cgi mods: 15.99491@1 and separately 15.99491@2
-    #[allow(clippy::unreadable_literal)]
-    let theoretical_fragments = &[
-        (132.047761, "M2-b1"),
-        (148.042671, "M1-b1"),
-        (150.058326, "M1-y1"),
-        (166.053236, "M2-y1"),
-        (297.093720, "precursor"),
-    ];
-    let model = Model::none()
-        .b(PrimaryIonSeries::default())
-        .y(PrimaryIonSeries::default());
-    test(
-        theoretical_fragments,
-        LinearPeptide::pro_forma("M[Oxidation#a1]M[#a1]", None)
-            .unwrap()
-            .into_linear()
-            .expect("Not a linear peptide"),
-        &model,
-        1,
-        true,
-        false,
-    );
-}
+// #[test]
+// fn with_possible_modifications() {
+//     // Compare rustyms with https://proteomicsresource.washington.edu/cgi-bin/fragment.cgi mods: 15.99491@1 and separately 15.99491@2
+//     #[expect(clippy::unreadable_literal)]
+//     let theoretical_fragments = &[
+//         (132.047761, "M2-b1"),
+//         (148.042671, "M1-b1"),
+//         (150.058326, "M1-y1"),
+//         (166.053236, "M2-y1"),
+//         (297.093720, "precursor"),
+//     ];
+//     let model = Model::none()
+//         .b(PrimaryIonSeries::default())
+//         .y(PrimaryIonSeries::default());
+//     test(
+//         theoretical_fragments,
+//         LinearPeptide::pro_forma("M[Oxidation#a1]M[#a1]", None)
+//             .unwrap()
+//             .into_linear()
+//             .expect("Not a linear peptide"),
+//         &model,
+//         1,
+//         true,
+//         false,
+//     );
+// }
 
-#[test]
-fn with_double_possible_modifications() {
-    // Manual addition over previous example
-    #[allow(clippy::unreadable_literal)]
-    let theoretical_fragments = &[
-        (132.047761, "b1"),
-        (148.042671, "b1+O"),
-        (164.038, "b1+O+O"),
-        (150.058326, "y1"),
-        (166.053236, "y1+O"),
-        (182.048, "y1+O+O"),
-        (313.089, "precursor"),
-    ];
-    let model = Model::none()
-        .b(PrimaryIonSeries::default())
-        .y(PrimaryIonSeries::default());
-    test(
-        theoretical_fragments,
-        LinearPeptide::pro_forma("M[Oxidation#a1][Oxidation#a2]M[#a1][#a2]", None)
-            .unwrap()
-            .into_linear()
-            .unwrap(),
-        &model,
-        1,
-        true,
-        false,
-    );
-}
+// #[test]
+// fn with_double_possible_modifications() {
+//     // Manual addition over previous example
+//     #[expect(clippy::unreadable_literal)]
+//     let theoretical_fragments = &[
+//         (132.047761, "b1"),
+//         (148.042671, "b1+O"),
+//         (164.038, "b1+O+O"),
+//         (150.058326, "y1"),
+//         (166.053236, "y1+O"),
+//         (182.048, "y1+O+O"),
+//         (313.089, "precursor"),
+//     ];
+//     let model = Model::none()
+//         .b(PrimaryIonSeries::default())
+//         .y(PrimaryIonSeries::default());
+//     test(
+//         theoretical_fragments,
+//         LinearPeptide::pro_forma("M[Oxidation#a1][Oxidation#a2]M[#a1][#a2]", None)
+//             .unwrap()
+//             .into_linear()
+//             .unwrap(),
+//         &model,
+//         1,
+//         true,
+//         false,
+//     );
+// }
 
 #[test]
 fn higher_charges() {
     // Compare rustyms with https://proteomicsresource.washington.edu/cgi-bin/fragment.cgi
-    #[allow(clippy::unreadable_literal)]
+    #[expect(clippy::unreadable_literal)]
     let theoretical_fragments = &[
         (9.615716, "a1+5"),
         (30.217553, "a2+5"),
@@ -177,7 +177,7 @@ fn higher_charges() {
     let model = Model::none().a(PrimaryIonSeries::default());
     test(
         theoretical_fragments,
-        LinearPeptide::pro_forma("ACD", None)
+        Peptidoform::pro_forma("ACD", None)
             .unwrap()
             .into_linear()
             .unwrap(),
@@ -191,7 +191,7 @@ fn higher_charges() {
 #[test]
 fn all_aminoacids() {
     // Compare rustyms with https://proteomicsresource.washington.edu/cgi-bin/fragment.cgi
-    #[allow(clippy::unreadable_literal)]
+    #[expect(clippy::unreadable_literal)]
     let theoretical_fragments = &[
         (44.049476, "a1"),
         (200.150587, "a2"),
@@ -337,7 +337,7 @@ fn all_aminoacids() {
         .z(PrimaryIonSeries::default());
     test(
         theoretical_fragments,
-        LinearPeptide::pro_forma("ARNDCQEGHILKMFPSTWYV", None)
+        Peptidoform::pro_forma("ARNDCQEGHILKMFPSTWYV", None)
             .unwrap()
             .into_linear()
             .unwrap(),
@@ -350,7 +350,7 @@ fn all_aminoacids() {
 
 #[test]
 fn glycan_structure_fragmentation() {
-    #[allow(clippy::unreadable_literal)]
+    #[expect(clippy::unreadable_literal)]
     let theoretical_fragments = &[
         (4593.06932015166, "pep+N4H5S1"),
         (4301.97390015166, "pep+N4H5"),
@@ -418,7 +418,7 @@ fn glycan_structure_fragmentation() {
     let model = Model::none().glycan(GlycanModel::DISALLOW.allow_structural(true));
     test(
         theoretical_fragments,
-        LinearPeptide::pro_forma("MVSHHN[GNO:G43728NL]LTTGATLINEQWLLTTAK", None)
+        Peptidoform::pro_forma("MVSHHN[GNO:G43728NL]LTTGATLINEQWLLTTAK", None)
             .unwrap()
             .into_linear()
             .unwrap(),
@@ -431,7 +431,7 @@ fn glycan_structure_fragmentation() {
 
 #[test]
 fn glycan_composition_fragmentation() {
-    #[allow(clippy::unreadable_literal)]
+    #[expect(clippy::unreadable_literal)]
     let theoretical_fragments = &[
         (4593.06932015166, "pep+N4H5S1"),
         (4301.97390015166, "pep+N4H5"),
@@ -498,7 +498,7 @@ fn glycan_composition_fragmentation() {
     let model = Model::none().glycan(GlycanModel::DISALLOW.compositional_range(0..=10));
     test(
         theoretical_fragments,
-        LinearPeptide::pro_forma("MVSHHN[Glycan:N4H5S1]LTTGATLINEQWLLTTAK", None)
+        Peptidoform::pro_forma("MVSHHN[Glycan:N4H5S1]LTTGATLINEQWLLTTAK", None)
             .unwrap()
             .into_linear()
             .unwrap(),
@@ -563,7 +563,7 @@ fn custom_database() -> CustomDatabase {
 
 #[test]
 fn intra_link() {
-    #[allow(clippy::unreadable_literal)]
+    #[expect(clippy::unreadable_literal)]
     let theoretical_fragments = &[
         (260.196, "y2+"),
         (407.265, "y3+"),
@@ -573,7 +573,7 @@ fn intra_link() {
         (732.327290402381, "b5+"),
     ];
     let peptide =
-        CompoundPeptidoform::pro_forma("K[C:DSSO#XL1]GK[#XL1]FLK", Some(&custom_database()))
+        CompoundPeptidoformIon::pro_forma("K[C:DSSO#XL1]GK[#XL1]FLK", Some(&custom_database()))
             .unwrap();
     let model = Model::none()
         .b(PrimaryIonSeries::default())
@@ -599,7 +599,7 @@ fn intra_link() {
 #[test]
 fn ensure_no_double_xl_labels_breaking() {
     let peptide =
-        CompoundPeptidoform::pro_forma("EVQLVESGGGLVQPGGSLRLSC[C:Disulfide#XL1]AASGFNIKDTYIHWVRQAPGKGLEWVARIYPTNGYTRYADSVKGRFTISADTSKNTAYLQMNSLRAEDTAVYYC[#XL1]SRWGGDGFYAMDYWGQGTLVTVSSASTKGPSVFPLAPSSKSTSGGTAALGC[C:Disulfide#XL2]LVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSSGLYSLSSVVTVPSSSLGTQTYIC[#XL2]NVNHKPSNTKVDKKVEPKSC[C:Disulfide#XL3]DKT//DIQMTQSPSSLSASVGDRVTITC[C:Disulfide#XL4]RASQDVNTAVAWYQQKPGKAPKLLIYSASFLYSGVPSRFSGSRSGTDFTLTISSLQPEDFATYYC[#XL4]QQHYTTPPTFGQGTKVEIKRTVAAPSVFIFPPSDEQLKSGTASVVC[C:Disulfide#XL5]LLNNFYPREAKVQWKVDNALQSGNSQESVTEQDSKDSTYSLSSTLTLSKADYEKHKVYAC[#XL5]EVTHQGLSSPVTKSFNRGEC[#XL3]", Some(&custom_database()))
+        CompoundPeptidoformIon::pro_forma("EVQLVESGGGLVQPGGSLRLSC[C:Disulfide#XL1]AASGFNIKDTYIHWVRQAPGKGLEWVARIYPTNGYTRYADSVKGRFTISADTSKNTAYLQMNSLRAEDTAVYYC[#XL1]SRWGGDGFYAMDYWGQGTLVTVSSASTKGPSVFPLAPSSKSTSGGTAALGC[C:Disulfide#XL2]LVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSSGLYSLSSVVTVPSSSLGTQTYIC[#XL2]NVNHKPSNTKVDKKVEPKSC[C:Disulfide#XL3]DKT//DIQMTQSPSSLSASVGDRVTITC[C:Disulfide#XL4]RASQDVNTAVAWYQQKPGKAPKLLIYSASFLYSGVPSRFSGSRSGTDFTLTISSLQPEDFATYYC[#XL4]QQHYTTPPTFGQGTKVEIKRTVAAPSVFIFPPSDEQLKSGTASVVC[C:Disulfide#XL5]LLNNFYPREAKVQWKVDNALQSGNSQESVTEQDSKDSTYSLSSTLTLSKADYEKHKVYAC[#XL5]EVTHQGLSSPVTKSFNRGEC[#XL3]", Some(&custom_database()))
             .unwrap();
     let model = Model::none()
         .b(PrimaryIonSeries::default())
@@ -629,7 +629,7 @@ fn ensure_no_double_xl_labels_breaking() {
 #[test]
 fn ensure_no_double_xl_labels_non_breaking() {
     let peptide =
-        CompoundPeptidoform::pro_forma("EVQLVESGGGLVQPGGSLRLSC[C:Disulfide#XL1]AASGFNIKDTYIHWVRQAPGKGLEWVARIYPTNGYTRYADSVKGRFTISADTSKNTAYLQMNSLRAEDTAVYYC[#XL1]SRWGGDGFYAMDYWGQGTLVTVSSASTKGPSVFPLAPSSKSTSGGTAALGC[C:Disulfide#XL2]LVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSSGLYSLSSVVTVPSSSLGTQTYIC[#XL2]NVNHKPSNTKVDKKVEPKSC[C:Disulfide#XL3]DKT//DIQMTQSPSSLSASVGDRVTITC[C:Disulfide#XL4]RASQDVNTAVAWYQQKPGKAPKLLIYSASFLYSGVPSRFSGSRSGTDFTLTISSLQPEDFATYYC[#XL4]QQHYTTPPTFGQGTKVEIKRTVAAPSVFIFPPSDEQLKSGTASVVC[C:Disulfide#XL5]LLNNFYPREAKVQWKVDNALQSGNSQESVTEQDSKDSTYSLSSTLTLSKADYEKHKVYAC[#XL5]EVTHQGLSSPVTKSFNRGEC[#XL3]", Some(&custom_database()))
+        CompoundPeptidoformIon::pro_forma("EVQLVESGGGLVQPGGSLRLSC[C:Disulfide#XL1]AASGFNIKDTYIHWVRQAPGKGLEWVARIYPTNGYTRYADSVKGRFTISADTSKNTAYLQMNSLRAEDTAVYYC[#XL1]SRWGGDGFYAMDYWGQGTLVTVSSASTKGPSVFPLAPSSKSTSGGTAALGC[C:Disulfide#XL2]LVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSSGLYSLSSVVTVPSSSLGTQTYIC[#XL2]NVNHKPSNTKVDKKVEPKSC[C:Disulfide#XL3]DKT//DIQMTQSPSSLSASVGDRVTITC[C:Disulfide#XL4]RASQDVNTAVAWYQQKPGKAPKLLIYSASFLYSGVPSRFSGSRSGTDFTLTISSLQPEDFATYYC[#XL4]QQHYTTPPTFGQGTKVEIKRTVAAPSVFIFPPSDEQLKSGTASVVC[C:Disulfide#XL5]LLNNFYPREAKVQWKVDNALQSGNSQESVTEQDSKDSTYSLSSTLTLSKADYEKHKVYAC[#XL5]EVTHQGLSSPVTKSFNRGEC[#XL3]", Some(&custom_database()))
             .unwrap();
     let model = Model::none()
         .b(PrimaryIonSeries::default())
@@ -658,7 +658,7 @@ fn ensure_no_double_xl_labels_non_breaking() {
 
 #[test]
 fn ensure_no_double_xl_labels_small_breaking() {
-    let peptide = CompoundPeptidoform::pro_forma(
+    let peptide = CompoundPeptidoformIon::pro_forma(
         "EC[C:Disulfide#XL1]AC[#XL1]SC[C:Disulfide#XL3]D//DC[#XL3]",
         Some(&custom_database()),
     )
@@ -678,7 +678,7 @@ fn ensure_no_double_xl_labels_small_breaking() {
 
 #[test]
 fn ensure_no_double_xl_labels_small_non_breaking() {
-    let peptide = CompoundPeptidoform::pro_forma(
+    let peptide = CompoundPeptidoformIon::pro_forma(
         "EC[C:Disulfide#XL1]AC[#XL1]SC[C:Disulfide#XL3]D//DC[#XL3]",
         Some(&custom_database()),
     )
@@ -698,7 +698,7 @@ fn ensure_no_double_xl_labels_small_non_breaking() {
 
 fn test(
     theoretical_fragments: &[(f64, &str)],
-    peptide: impl Into<CompoundPeptidoform>,
+    peptide: impl Into<CompoundPeptidoformIon>,
     model: &Model,
     charge: usize,
     allow_left_over_generated: bool,
diff --git a/rustyms/src/glycan/glycan_structure.rs b/rustyms/src/glycan/glycan_structure.rs
index c7f2df98..c6be1d90 100644
--- a/rustyms/src/glycan/glycan_structure.rs
+++ b/rustyms/src/glycan/glycan_structure.rs
@@ -175,7 +175,7 @@ impl GlycanStructure {
 }
 
 #[cfg(test)]
-#[allow(clippy::missing_panics_doc)]
+#[expect(clippy::missing_panics_doc)]
 mod test {
     use super::*;
 
diff --git a/rustyms/src/glycan/monosaccharide.rs b/rustyms/src/glycan/monosaccharide.rs
index 2bc1ad15..c7c58e7d 100644
--- a/rustyms/src/glycan/monosaccharide.rs
+++ b/rustyms/src/glycan/monosaccharide.rs
@@ -45,8 +45,8 @@ impl MonoSaccharide {
     pub(crate) fn theoretical_fragments(
         composition: &[(Self, isize)],
         model: &Model,
+        peptidoform_ion_index: usize,
         peptidoform_index: usize,
-        peptide_index: usize,
         charge_carriers: &mut CachedCharge,
         full_formula: &Multi<MolecularFormula>,
         attachment: Option<(AminoAcid, usize)>,
@@ -64,15 +64,15 @@ impl MonoSaccharide {
             let formula: MolecularFormula = composition
                 .iter()
                 .map(|s| {
-                    s.0.formula_inner(SequencePosition::default(), peptide_index) * s.1 as i32
+                    s.0.formula_inner(SequencePosition::default(), peptidoform_index) * s.1 as i32
                 })
                 .sum();
             fragments.extend(
                 Fragment::new(
                     formula.clone(),
                     Charge::default(),
+                    peptidoform_ion_index,
                     peptidoform_index,
-                    peptide_index,
                     FragmentType::OxoniumComposition(composition.clone(), attachment),
                 )
                 .with_charge_range(charge_carriers, model.glycan.oxonium_charge_range)
@@ -82,8 +82,8 @@ impl MonoSaccharide {
                 Fragment::new(
                     base - &formula,
                     Charge::default(),
+                    peptidoform_ion_index,
                     peptidoform_index,
-                    peptide_index,
                     FragmentType::YComposition(composition.clone(), attachment),
                 )
                 .with_charge_range(charge_carriers, model.glycan.other_charge_range)
@@ -96,8 +96,8 @@ impl MonoSaccharide {
             fragments.extend(
                 sugar
                     .diagnostic_ions(
+                        peptidoform_ion_index,
                         peptidoform_index,
-                        peptide_index,
                         DiagnosticPosition::GlycanCompositional(sugar.clone(), attachment),
                         false,
                     )
@@ -162,16 +162,16 @@ impl MonoSaccharide {
     /// According to: <https://doi.org/10.1016/j.trac.2018.09.007>.
     pub(crate) fn diagnostic_ions(
         &self,
+        peptidoform_ion_index: usize,
         peptidoform_index: usize,
-        peptide_index: usize,
         position: DiagnosticPosition,
         add_base: bool,
     ) -> Vec<Fragment> {
         let base = Fragment::new(
             self.formula(),
             Charge::default(),
+            peptidoform_ion_index,
             peptidoform_index,
-            peptide_index,
             FragmentType::Diagnostic(position),
         );
         let mut result =
@@ -220,7 +220,7 @@ impl MonoSaccharide {
 }
 
 #[cfg(test)]
-#[allow(clippy::missing_panics_doc)]
+#[expect(clippy::missing_panics_doc)]
 mod tests {
     use super::*;
 
diff --git a/rustyms/src/glycan/positioned_structure.rs b/rustyms/src/glycan/positioned_structure.rs
index 8418d1ce..81741d0f 100644
--- a/rustyms/src/glycan/positioned_structure.rs
+++ b/rustyms/src/glycan/positioned_structure.rs
@@ -29,13 +29,13 @@ impl Chemical for PositionedGlycanStructure {
     fn formula_inner(
         &self,
         sequence_index: SequencePosition,
-        peptide_index: usize,
+        peptidoform_index: usize,
     ) -> MolecularFormula {
-        self.sugar.formula_inner(sequence_index, peptide_index)
+        self.sugar.formula_inner(sequence_index, peptidoform_index)
             + self
                 .branches
                 .iter()
-                .map(|f| f.formula_inner(sequence_index, peptide_index))
+                .map(|f| f.formula_inner(sequence_index, peptidoform_index))
                 .sum::<MolecularFormula>()
     }
 }
@@ -46,8 +46,8 @@ impl PositionedGlycanStructure {
     pub fn generate_theoretical_fragments(
         &self,
         model: &Model,
+        peptidoform_ion_index: usize,
         peptidoform_index: usize,
-        peptide_index: usize,
         charge_carriers: &mut CachedCharge,
         full_formula: &Multi<MolecularFormula>,
         attachment: Option<(AminoAcid, usize)>,
@@ -58,7 +58,7 @@ impl PositionedGlycanStructure {
             .then(|| {
                 // Get all base fragments from this node and all its children
                 let mut base_fragments = self
-                    .oxonium_fragments(peptidoform_index, peptide_index, attachment)
+                    .oxonium_fragments(peptidoform_ion_index, peptidoform_index, attachment)
                     .into_iter()
                     .flat_map(|f| {
                         f.with_charge_range(charge_carriers, model.glycan.oxonium_charge_range)
@@ -67,7 +67,7 @@ impl PositionedGlycanStructure {
                     .collect_vec();
                 // Generate all Y fragments
                 base_fragments.extend(
-                    self.internal_break_points(peptide_index, attachment)
+                    self.internal_break_points(peptidoform_index, attachment)
                         .iter()
                         .filter(|(_, bonds)| {
                             bonds.iter().all(|b| !matches!(b, GlycanBreakPos::B(_)))
@@ -76,12 +76,13 @@ impl PositionedGlycanStructure {
                         .flat_map(move |(f, bonds)| {
                             full_formula.iter().map(move |full| {
                                 Fragment::new(
-                                    full - self
-                                        .formula_inner(SequencePosition::default(), peptide_index)
-                                        + f,
+                                    full - self.formula_inner(
+                                        SequencePosition::default(),
+                                        peptidoform_index,
+                                    ) + f,
                                     Charge::zero(),
+                                    peptidoform_ion_index,
                                     peptidoform_index,
-                                    peptide_index,
                                     FragmentType::Y(
                                         bonds
                                             .iter()
@@ -100,7 +101,7 @@ impl PositionedGlycanStructure {
                 );
                 // Generate all diagnostic ions
                 base_fragments.extend(
-                    self.diagnostic_ions(peptidoform_index, peptide_index, attachment)
+                    self.diagnostic_ions(peptidoform_ion_index, peptidoform_index, attachment)
                         .into_iter()
                         .flat_map(|f| {
                             f.with_charge_range(charge_carriers, model.glycan.oxonium_charge_range)
@@ -114,13 +115,13 @@ impl PositionedGlycanStructure {
     /// Get uncharged diagnostic ions from all positions
     fn diagnostic_ions(
         &self,
+        peptidoform_ion_index: usize,
         peptidoform_index: usize,
-        peptide_index: usize,
         attachment: Option<(AminoAcid, usize)>,
     ) -> Vec<Fragment> {
         let mut output = self.sugar.diagnostic_ions(
+            peptidoform_ion_index,
             peptidoform_index,
-            peptide_index,
             crate::fragment::DiagnosticPosition::Glycan(
                 self.position(attachment),
                 self.sugar.clone(),
@@ -128,9 +129,9 @@ impl PositionedGlycanStructure {
             true,
         );
         output.extend(
-            self.branches
-                .iter()
-                .flat_map(|b| b.diagnostic_ions(peptidoform_index, peptide_index, attachment)),
+            self.branches.iter().flat_map(|b| {
+                b.diagnostic_ions(peptidoform_ion_index, peptidoform_index, attachment)
+            }),
         );
 
         output
@@ -139,21 +140,21 @@ impl PositionedGlycanStructure {
     /// Generate all fragments without charge and neutral loss options
     fn oxonium_fragments(
         &self,
+        peptidoform_ion_index: usize,
         peptidoform_index: usize,
-        peptide_index: usize,
         attachment: Option<(AminoAcid, usize)>,
     ) -> Vec<Fragment> {
         // Generate the basic single breakage B fragments
         let mut base_fragments = vec![Fragment::new(
-            self.formula_inner(SequencePosition::default(), peptide_index),
+            self.formula_inner(SequencePosition::default(), peptidoform_index),
             Charge::zero(),
+            peptidoform_ion_index,
             peptidoform_index,
-            peptide_index,
             FragmentType::B(self.position(attachment)),
         )];
         // Extend with all internal fragments, meaning multiple breaking bonds
         base_fragments.extend(
-            self.internal_break_points(peptide_index, attachment)
+            self.internal_break_points(peptidoform_index, attachment)
                 .into_iter()
                 .filter(|(_, breakages)| {
                     !breakages
@@ -171,25 +172,23 @@ impl PositionedGlycanStructure {
                     Fragment::new(
                         formula,
                         Charge::zero(),
+                        peptidoform_ion_index,
                         peptidoform_index,
-                        peptide_index,
                         FragmentType::Oxonium(breakages),
                     )
                 }),
         );
         // Extend with the theoretical fragments for all branches of this position
-        base_fragments.extend(
-            self.branches
-                .iter()
-                .flat_map(|b| b.oxonium_fragments(peptidoform_index, peptide_index, attachment)),
-        );
+        base_fragments.extend(self.branches.iter().flat_map(|b| {
+            b.oxonium_fragments(peptidoform_ion_index, peptidoform_index, attachment)
+        }));
         base_fragments
     }
 
     /// All possible bonds that can be broken and the molecular formula that would be held over if these bonds all broke and the broken off parts are lost.
     fn internal_break_points(
         &self,
-        peptide_index: usize,
+        peptidoform_index: usize,
         attachment: Option<(AminoAcid, usize)>,
     ) -> Vec<(MolecularFormula, Vec<GlycanBreakPos>)> {
         // Find every internal fragment ending at this bond (in a B breakage) (all bonds found are Y breakages and endings)
@@ -197,7 +196,7 @@ impl PositionedGlycanStructure {
         if self.branches.is_empty() {
             vec![
                 (
-                    self.formula_inner(SequencePosition::default(), peptide_index),
+                    self.formula_inner(SequencePosition::default(), peptidoform_index),
                     vec![GlycanBreakPos::End(self.position(attachment))],
                 ),
                 (
@@ -208,7 +207,7 @@ impl PositionedGlycanStructure {
         } else {
             self.branches
                 .iter()
-                .map(|b| b.internal_break_points(peptide_index, attachment)) // get all previous options
+                .map(|b| b.internal_break_points(peptidoform_index, attachment)) // get all previous options
                 .fold(Vec::new(), |accumulator, branch_options| {
                     if accumulator.is_empty() {
                         branch_options
@@ -230,7 +229,7 @@ impl PositionedGlycanStructure {
                     (
                         m + self
                             .sugar
-                            .formula_inner(SequencePosition::default(), peptide_index),
+                            .formula_inner(SequencePosition::default(), peptidoform_index),
                         b,
                     )
                 })
diff --git a/rustyms/src/helper_functions.rs b/rustyms/src/helper_functions.rs
index a3074fcb..f10dd7a0 100644
--- a/rustyms/src/helper_functions.rs
+++ b/rustyms/src/helper_functions.rs
@@ -24,7 +24,6 @@ pub fn peptide_range_contains(
 pub trait ResultExtensions<T, E> {
     /// # Errors
     /// If any of the errors contained within has an error.
-    #[allow(dead_code)]
     fn flat_err(self) -> Result<T, E>;
 }
 
@@ -49,7 +48,6 @@ impl<T, E> ResultExtensions<T, E> for Result<Result<T, E>, E> {
 pub trait InvertResult<T, E> {
     /// # Errors
     /// If any of the errors contained within has an error.
-    #[allow(dead_code)]
     fn invert(self) -> Result<Option<T>, E>;
 }
 
@@ -58,6 +56,12 @@ impl<T, E> InvertResult<T, E> for Option<Result<T, E>> {
         self.map_or_else(|| Ok(None), |o| o.map(|v| Some(v)))
     }
 }
+impl<T, E> InvertResult<T, E> for Option<Option<Result<T, E>>> {
+    fn invert(self) -> Result<Option<T>, E> {
+        self.flatten()
+            .map_or_else(|| Ok(None), |o| o.map(|v| Some(v)))
+    }
+}
 impl<T, E> InvertResult<T, E> for Option<Result<Option<T>, E>> {
     fn invert(self) -> Result<Option<T>, E> {
         self.map_or_else(|| Ok(None), |o| o)
@@ -167,7 +171,6 @@ impl RangeMaths<usize> for Range<usize> {
 
 /// # Errors
 /// If the name cannot be recognised or a number is not valid.
-#[allow(dead_code)]
 pub fn parse_named_counter<T: Clone>(
     value: &str,
     names: &[(String, T)],
@@ -240,10 +243,9 @@ pub fn check_extension(filename: impl AsRef<Path>, extension: impl AsRef<Path>)
     filename
         .as_ref()
         .extension()
-        .map_or(false, |ext| ext.eq_ignore_ascii_case(extension.as_ref()))
+        .is_some_and(|ext| ext.eq_ignore_ascii_case(extension.as_ref()))
 }
 
-#[allow(dead_code)]
 /// Get the index of the next copy of the given char (looking at the byte value, does not guarantee full character)
 pub fn next_char(chars: &[u8], start: usize, char: u8) -> Option<usize> {
     for (i, ch) in chars[start..].iter().enumerate() {
@@ -254,7 +256,6 @@ pub fn next_char(chars: &[u8], start: usize, char: u8) -> Option<usize> {
     None
 }
 
-#[allow(dead_code)]
 /// Find the enclosed text by the given symbols, assumes a single open is already read just before the start, guarantees to only pick full characters
 pub fn end_of_enclosure(text: &str, start: usize, open: u8, close: u8) -> Option<usize> {
     let mut state = 1;
@@ -274,7 +275,6 @@ pub fn end_of_enclosure(text: &str, start: usize, open: u8, close: u8) -> Option
     None
 }
 
-#[allow(dead_code)]
 /// Find the enclosed text by the given symbols, assumes a single open is already read just before the start.
 /// This also takes brackets '[]' into account and these take precedence over the enclosure searched for.
 pub fn end_of_enclosure_with_brackets(
@@ -311,7 +311,6 @@ pub fn end_of_enclosure_with_brackets(
     None
 }
 
-#[allow(dead_code)]
 /// Get the next number, returns length in bytes and the number.
 /// # Panics
 /// If the text is not valid UTF-8.
@@ -350,7 +349,6 @@ pub fn next_num(chars: &[u8], mut start: usize, allow_only_sign: bool) -> Option
 /// A number of characters, used as length or index
 pub type Characters = usize;
 
-#[allow(dead_code)]
 /// Get the next number starting at the character range given, returns length in characters and the number.
 /// # Errors
 /// Returns none if the number is too big to fit in a `isize`.
@@ -453,7 +451,7 @@ macro_rules! impl_binop_ref_cases {
 }
 
 /// To be used as `The xx number ` + the explanation from here (does not have a dot).
-pub fn explain_number_error(error: &ParseIntError) -> &'static str {
+pub const fn explain_number_error(error: &ParseIntError) -> &'static str {
     match error.kind() {
         IntErrorKind::Empty => "is empty",
         IntErrorKind::InvalidDigit => "contains an invalid character",
diff --git a/rustyms/src/identification/common_parser.rs b/rustyms/src/identification/common_parser.rs
index 3d9e8b25..bd08fbe8 100644
--- a/rustyms/src/identification/common_parser.rs
+++ b/rustyms/src/identification/common_parser.rs
@@ -27,7 +27,7 @@ macro_rules! format_family {
         #[non_exhaustive]
         #[derive(Clone, PartialEq, Debug, Default, Serialize, Deserialize)]
         #[doc = $data_doc]
-        #[allow(missing_docs)]
+        #[expect(missing_docs)]
         pub struct $data {
             $($(#[doc = $rdoc])? pub $rname: $rtyp,)*
             $($(#[doc = $odoc])? pub $oname: Option<$otyp>,)*
@@ -167,7 +167,7 @@ impl<'a> Location<'a> {
         self.location.len()
     }
 
-    #[allow(dead_code)]
+    #[expect(dead_code)]
     pub fn column(column: usize, source: &'a CsvLine) -> Self {
         Location {
             line: source,
@@ -175,7 +175,7 @@ impl<'a> Location<'a> {
         }
     }
 
-    #[allow(dead_code)]
+    #[expect(dead_code)]
     pub fn optional_column(column: Option<usize>, source: &'a CsvLine) -> Option<Self> {
         column.map(|index| Location {
             line: source,
@@ -183,7 +183,6 @@ impl<'a> Location<'a> {
         })
     }
 
-    #[allow(clippy::needless_pass_by_value)]
     pub fn array(self, sep: char) -> std::vec::IntoIter<Self> {
         let mut offset = 0;
         let mut output = Vec::new();
@@ -309,9 +308,24 @@ impl<'a> Location<'a> {
     pub fn apply(self, f: impl FnOnce(Self) -> Self) -> Self {
         f(self)
     }
+
+    pub fn split_once(self, p: char) -> Option<(Self, Self)> {
+        self.as_str().split_once(p).map(|(start, end)| {
+            (
+                Self {
+                    line: self.line,
+                    location: self.location.start..self.location.start + start.len(),
+                },
+                Self {
+                    line: self.line,
+                    location: self.location.end - end.len()..self.location.end,
+                },
+            )
+        })
+    }
 }
 
-#[allow(dead_code)]
+#[expect(dead_code)]
 pub trait OptionalLocation<'a> {
     fn or_empty(self) -> Option<Location<'a>>;
     /// # Errors
diff --git a/rustyms/src/identification/deepnovofamily.rs b/rustyms/src/identification/deepnovofamily.rs
index 855bb433..2cb8b9b4 100644
--- a/rustyms/src/identification/deepnovofamily.rs
+++ b/rustyms/src/identification/deepnovofamily.rs
@@ -4,9 +4,9 @@ use crate::{
     error::CustomError,
     identification::PeaksFamilyId,
     ontologies::CustomDatabase,
-    peptide::{SemiAmbiguous, SloppyParsingParameters},
+    peptidoform::{SemiAmbiguous, SloppyParsingParameters},
     system::{usize::Charge, MassOverCharge},
-    LinearPeptide,
+    Peptidoform,
 };
 
 use serde::{Deserialize, Serialize};
@@ -38,8 +38,8 @@ format_family!(
         scan: Vec<PeaksFamilyId>, |location: Location, _| location.or_empty()
             .map_or(Ok(Vec::new()), |l| l.array(';').map(|v| v.parse(ID_ERROR)).collect::<Result<Vec<_>,_>>());
 
-        peptide: Option<LinearPeptide<SemiAmbiguous>>, |location: Location, custom_database: Option<&CustomDatabase>|
-                location.or_empty().map(|location| LinearPeptide::sloppy_pro_forma(
+        peptide: Option<Peptidoform<SemiAmbiguous>>, |location: Location, custom_database: Option<&CustomDatabase>|
+                location.or_empty().map(|location| Peptidoform::sloppy_pro_forma(
                     location.full_line(),
                     location.location.clone(),
                     custom_database,
@@ -68,7 +68,7 @@ format_family!(
 
     fn post_process(_source: &CsvLine, mut parsed: Self, _custom_database: Option<&CustomDatabase>) -> Result<Self, CustomError> {
         if parsed.local_confidence.as_ref().map(Vec::len)
-            != parsed.peptide.as_ref().map(LinearPeptide::len)
+            != parsed.peptide.as_ref().map(Peptidoform::len)
         {
             parsed.local_confidence = parsed.local_confidence.map(interpolate_lc);
         }
@@ -90,7 +90,7 @@ impl From<DeepNovoFamilyData> for IdentifiedPeptide {
 }
 
 /// Interpolate the local confidence when the confidence between AAs is used instead of the confidence of a single AA
-#[allow(clippy::needless_pass_by_value)] // The return value will replace the given value, so moving is fine
+#[expect(clippy::needless_pass_by_value)] // The return value will replace the given value, so moving is fine
 fn interpolate_lc(local_confidence: Vec<f64>) -> Vec<f64> {
     let mut reinterpolated = Vec::with_capacity(local_confidence.len() + 1);
 
@@ -131,7 +131,6 @@ pub const POINTNOVOFAMILY: DeepNovoFamilyFormat = DeepNovoFamilyFormat {
 
 /// All possible DeepNovoFamily versions
 #[derive(Clone, Eq, PartialEq, Ord, PartialOrd, Hash, Debug, Default, Serialize, Deserialize)]
-#[allow(non_camel_case_types)]
 pub enum DeepNovoFamilyVersion {
     #[default]
     /// DeepNovo version 0.0.1
diff --git a/rustyms/src/identification/fasta.rs b/rustyms/src/identification/fasta.rs
index 6261f0f2..08c6c98e 100644
--- a/rustyms/src/identification/fasta.rs
+++ b/rustyms/src/identification/fasta.rs
@@ -2,8 +2,8 @@ use crate::{
     error::{Context, CustomError},
     helper_functions::explain_number_error,
     identification::{IdentifiedPeptide, MetaData},
-    peptide::{AnnotatedPeptide, Annotation, Region, SemiAmbiguous},
-    AminoAcid, LinearPeptide, SequenceElement,
+    peptidoform::{AnnotatedPeptide, Annotation, Region, SemiAmbiguous},
+    AminoAcid, Peptidoform, SequenceElement,
 };
 use itertools::Itertools;
 use serde::{Deserialize, Serialize};
@@ -24,14 +24,26 @@ pub struct FastaData {
     tags: Vec<(Range<usize>, Range<usize>)>,
     line_index: usize,
     full_header: String,
-    peptide: LinearPeptide<SemiAmbiguous>,
+    peptide: Peptidoform<SemiAmbiguous>,
     regions: Vec<(Region, usize)>,
     annotations: Vec<(Annotation, usize)>,
 }
 
+impl std::cmp::Ord for FastaData {
+    fn cmp(&self, other: &Self) -> std::cmp::Ordering {
+        self.line_index.cmp(&other.line_index)
+    }
+}
+
+impl std::cmp::PartialOrd for FastaData {
+    fn partial_cmp(&self, other: &Self) -> Option<std::cmp::Ordering> {
+        Some(self.cmp(other))
+    }
+}
+
 impl AnnotatedPeptide for FastaData {
     type Complexity = SemiAmbiguous;
-    fn peptide(&self) -> &LinearPeptide<SemiAmbiguous> {
+    fn peptide(&self) -> &Peptidoform<SemiAmbiguous> {
         &self.peptide
     }
     fn regions(&self) -> &[(Region, usize)] {
@@ -43,9 +55,9 @@ impl AnnotatedPeptide for FastaData {
 }
 
 /// A fasta identifier following the NCBI identifier definition
-#[allow(missing_docs)]
+#[expect(missing_docs)]
 #[derive(Clone, PartialEq, Eq, PartialOrd, Ord, Debug, Serialize, Deserialize, Hash)]
-#[allow(clippy::upper_case_acronyms)]
+#[expect(clippy::upper_case_acronyms)]
 pub enum FastaIdentifier<T> {
     Undefined(T),
     Local(T),
@@ -139,7 +151,11 @@ impl FastaIdentifier<Range<usize>> {
             Self::GenInfoIntegratedDatabase(a) => {
                 FastaIdentifier::GenInfoIntegratedDatabase(header[a.clone()].to_string())
             }
-            Self::Undefined(a) => FastaIdentifier::Undefined(header[a.clone()].to_string()),
+            Self::Undefined(a) => FastaIdentifier::Undefined(
+                header
+                    .get(a.clone())
+                    .map_or(String::new(), ToString::to_string),
+            ),
             Self::Local(a) => FastaIdentifier::Local(header[a.clone()].to_string()),
             Self::GenBank(a, b) => FastaIdentifier::GenBank(
                 header[a.clone()].to_string(),
@@ -202,7 +218,35 @@ impl FastaIdentifier<Range<usize>> {
     }
 }
 
-impl<'a> std::fmt::Display for FastaIdentifier<&'a str> {
+impl std::fmt::Display for FastaIdentifier<&'_ str> {
+    fn fmt(&self, f: &mut std::fmt::Formatter<'_>) -> std::fmt::Result {
+        match self {
+            Self::GenInfoBackboneSeqID(a) => write!(f, "bbs|{a}"),
+            Self::GenInfoBackboneMolType(a) => write!(f, "bbm|{a}"),
+            Self::GenInfoImportID(a) => write!(f, "gim|{a}"),
+            Self::GenInfoIntegratedDatabase(a) => write!(f, "gi|{a}"),
+            Self::GenBank(a, b) => write!(f, "gb|{a}|{b}"),
+            Self::EMBL(a, b) => write!(f, "emb|{a}|{b}"),
+            Self::PIR(a, b) => write!(f, "pir|{a}|{b}"),
+            Self::SwissProt(a, b) => write!(f, "sp|{a}|{b}"),
+            Self::Patent(a, b, c) => write!(f, "pat|{a}|{b}|{c}"),
+            Self::PrePatent(a, b, c) => write!(f, "pgp|{a}|{b}|{c}"),
+            Self::RefSeq(a, b) => write!(f, "ref|{a}|{b}"),
+            Self::GeneralDatabase(b, a) => write!(f, "gnl|{a}|{b}"),
+            Self::DDBJ(a, b) => write!(f, "dbj|{a}|{b}"),
+            Self::PRF(a, b) => write!(f, "prf|{a}|{b}"),
+            Self::ThirdPartyGenBank(a, b) => write!(f, "tpg|{a}|{b}"),
+            Self::ThirdPartyEMBL(a, b) => write!(f, "tpe|{a}|{b}"),
+            Self::ThirdPartyDDJ(a, b) => write!(f, "tpd|{a}|{b}"),
+            Self::TrEMBL(a, b) => write!(f, "tr|{a}|{b}"),
+            Self::Undefined(a) => write!(f, "{a}"),
+            Self::Local(a) => write!(f, "lcl|{a}"),
+            Self::PDB(a, b) => write!(f, "pdb|{a}|{b}"),
+        }
+    }
+}
+
+impl std::fmt::Display for FastaIdentifier<String> {
     fn fmt(&self, f: &mut std::fmt::Formatter<'_>) -> std::fmt::Result {
         match self {
             Self::GenInfoBackboneSeqID(a) => write!(f, "bbs|{a}"),
@@ -431,7 +475,7 @@ impl FastaData {
     }
 
     /// Get the sequence
-    pub const fn peptide(&self) -> &LinearPeptide<SemiAmbiguous> {
+    pub const fn peptide(&self) -> &Peptidoform<SemiAmbiguous> {
         &self.peptide
     }
 
@@ -469,7 +513,6 @@ impl FastaData {
                     path.map_or(Context::None, |p| Context::show(p.to_string_lossy())),
                 )
             })?;
-            #[allow(clippy::manual_strip)]
             if line.starts_with('>') {
                 if let Some(last_header) = last_header {
                     sequences.push(
@@ -545,7 +588,7 @@ impl FastaData {
 
     /// # Errors
     /// When the parsing of the fasta identifier is not succesful
-    #[allow(clippy::missing_panics_doc)] // Regions and annotation parse cannot fail
+    #[expect(clippy::missing_panics_doc)] // Regions and annotation parse cannot fail
     fn parse_header(line_index: usize, full_header: String) -> Result<Self, CustomError> {
         // thread 'main' panicked at C:\Users\5803969\src\rustyms\rustyms\src\identification\fasta.rs:301:26:
         // begin <= end (16 <= 15) when slicing `>Trastuzumab_HC REGIONS=FR1:25;CDR1:8;FR2:17;CDR2:8;FR3:38;CDR3:13;FR4:11;CH1:98;H:15;CH2:110;CH3:105;CHS:2 ANNOTATIONS=C:21;C:5;C:80;C:95;C:109;C:110;C:112;C:146;C:160;C:202;C:217;C:263;C:279;N:299;C:323;C:338;C:369;C:383;C:412;C:427;C:443`
@@ -661,7 +704,7 @@ impl FastaData {
             annotations,
             full_header,
             line_index,
-            peptide: LinearPeptide::default(),
+            peptide: Peptidoform::default(),
         })
     }
 }
@@ -683,19 +726,19 @@ impl From<FastaData> for IdentifiedPeptide {
 }
 
 #[test]
-#[allow(clippy::missing_panics_doc)]
+#[expect(clippy::missing_panics_doc)]
 fn empty_lines() {
     let file = ">A\naaa\n\naaa";
     let fasta = FastaData::parse_reader(BufReader::new(file.as_bytes()), None).unwrap();
     assert_eq!(fasta.len(), 1);
     assert_eq!(
         fasta[0].peptide,
-        LinearPeptide::pro_forma("AAAAAA", None).unwrap()
+        Peptidoform::pro_forma("AAAAAA", None).unwrap()
     );
 }
 
 #[test]
-#[allow(clippy::missing_panics_doc)]
+#[expect(clippy::missing_panics_doc)]
 fn parse_header() {
     let header = ">sp|UniqueIdentifier|EntryName ProteinName OS=OrganismName OX=OrganismIdentifier PE=ProteinExistence SV=SequenceVersion REGIONS=FR1:12;CDR1:6;FR2:13 ANNOTATIONS=C:12;Conserved:25";
     let header = FastaData::parse_header(0, header.to_string()).unwrap();
diff --git a/rustyms/src/identification/general.rs b/rustyms/src/identification/general.rs
index 1aafc038..2f068c58 100644
--- a/rustyms/src/identification/general.rs
+++ b/rustyms/src/identification/general.rs
@@ -128,7 +128,7 @@ pub fn open_identified_peptides_file<'a>(
     }
 }
 
-#[allow(clippy::missing_panics_doc)]
+#[expect(clippy::missing_panics_doc)]
 #[cfg(test)]
 mod tests {
     use super::*;
diff --git a/rustyms/src/identification/identified_peptide.rs b/rustyms/src/identification/identified_peptide.rs
index 3a71bd5d..054ee678 100644
--- a/rustyms/src/identification/identified_peptide.rs
+++ b/rustyms/src/identification/identified_peptide.rs
@@ -12,27 +12,20 @@ use crate::{
     error::CustomError,
     formula::MultiChemical,
     identification::{
-        deepnovofamily::DeepNovoFamilyData,
-        fasta::{FastaData, FastaIdentifier},
-        instanovo::InstaNovoData,
-        novob::NovoBData,
-        novor::NovorData,
-        opair::OpairData,
-        peaks::PeaksData,
-        pepnet::PepNetData,
-        plink::PLinkData,
-        powernovo::PowerNovoData,
-        system::MassOverCharge,
-        MSFraggerData, MZTabData, MaxQuantData, PLGSData, SageData, SpectrumSequenceListData,
+        deepnovofamily::DeepNovoFamilyData, fasta::FastaData, fasta::FastaIdentifier,
+        instanovo::InstaNovoData, novob::NovoBData, novor::NovorData, opair::OpairData,
+        peaks::PeaksData, pepnet::PepNetData, plink::PLinkData, powernovo::PowerNovoData,
+        system::MassOverCharge, MSFraggerData, MZTabData, MaxQuantData, PLGSData, SageData,
+        SpectrumSequenceListData,
     },
     ontologies::CustomDatabase,
-    peptide::{SemiAmbiguous, SimpleLinear},
+    peptidoform::{SemiAmbiguous, SimpleLinear},
     system::usize::Charge,
     system::{OrderedTime, Time},
-    Fragment, LinearPeptide, Peptidoform,
+    Peptidoform, PeptidoformIon,
 };
 
-use super::CompoundPeptidoform;
+use super::CompoundPeptidoformIon;
 
 /// A peptide that is identified by a de novo or database matching program
 #[derive(Clone, PartialEq, Debug, Serialize, Deserialize)]
@@ -47,7 +40,7 @@ pub struct IdentifiedPeptide {
 
 /// The definition of all special metadata for all types of identified peptides that can be read
 #[derive(Clone, PartialEq, Debug, Serialize, Deserialize)]
-#[allow(clippy::large_enum_variant, clippy::upper_case_acronyms)]
+#[expect(clippy::upper_case_acronyms)]
 pub enum MetaData {
     /// DeepNovo/PointNovo/PGPointNovo metadata
     DeepNovoFamily(DeepNovoFamilyData),
@@ -87,20 +80,20 @@ pub enum MetaData {
 #[derive(Debug, Clone)]
 pub enum ReturnedPeptide<'a> {
     /// A semi ambiguous linear peptide
-    LinearSemiAmbiguous(&'a LinearPeptide<SemiAmbiguous>),
+    LinearSemiAmbiguous(&'a Peptidoform<SemiAmbiguous>),
     /// A simple linear peptide
-    LinearSimpleLinear(&'a LinearPeptide<SimpleLinear>),
+    LinearSimpleLinear(&'a Peptidoform<SimpleLinear>),
     /// A (potentially) cross-linked peptidoform
-    Peptidoform(&'a Peptidoform),
+    Peptidoform(&'a PeptidoformIon),
     /// A (potentially) cross-linked chimeric set of peptidoforms
-    CompoundPeptidoform(Cow<'a, CompoundPeptidoform>),
+    CompoundPeptidoform(Cow<'a, CompoundPeptidoformIon>),
 }
 
-impl<'a> MultiChemical for ReturnedPeptide<'a> {
+impl MultiChemical for ReturnedPeptide<'_> {
     fn formulas_inner(
         &self,
         _sequence_index: super::SequencePosition,
-        _peptide_index: usize,
+        _peptidoform_index: usize,
     ) -> super::Multi<super::MolecularFormula> {
         match self {
             Self::LinearSemiAmbiguous(p) => p.formulas(),
@@ -111,7 +104,7 @@ impl<'a> MultiChemical for ReturnedPeptide<'a> {
     }
 }
 
-impl<'a> std::fmt::Display for ReturnedPeptide<'a> {
+impl std::fmt::Display for ReturnedPeptide<'_> {
     fn fmt(&self, f: &mut std::fmt::Formatter<'_>) -> std::fmt::Result {
         match self {
             Self::LinearSemiAmbiguous(p) => write!(f, "{p}"),
@@ -122,10 +115,9 @@ impl<'a> std::fmt::Display for ReturnedPeptide<'a> {
     }
 }
 
-#[allow(dead_code)]
 impl<'a> ReturnedPeptide<'a> {
     /// Get the underlying peptide, or None if the underlying result was a peptidoform
-    pub fn peptide(self) -> Option<Cow<'a, LinearPeptide<SimpleLinear>>> {
+    pub fn peptide(self) -> Option<Cow<'a, Peptidoform<SimpleLinear>>> {
         match self {
             Self::LinearSemiAmbiguous(p) => Some(Cow::Owned(p.clone().into())),
             Self::LinearSimpleLinear(p) => Some(Cow::Borrowed(p)),
@@ -133,7 +125,7 @@ impl<'a> ReturnedPeptide<'a> {
         }
     }
     /// Get the underlying result as a peptidoform, if it was a peptide make a new peptidoform from it
-    pub fn peptidoform(self) -> Option<Cow<'a, Peptidoform>> {
+    pub fn peptidoform(self) -> Option<Cow<'a, PeptidoformIon>> {
         match self {
             Self::LinearSemiAmbiguous(p) => Some(Cow::Owned(p.clone().into())),
             Self::LinearSimpleLinear(p) => Some(Cow::Owned(p.clone().into())),
@@ -142,7 +134,7 @@ impl<'a> ReturnedPeptide<'a> {
         }
     }
     /// Get the underlying result as a compound peptidoform, if it was a peptide make a new peptidoform from it
-    pub fn compound_peptidoform(self) -> Cow<'a, CompoundPeptidoform> {
+    pub fn compound_peptidoform(self) -> Cow<'a, CompoundPeptidoformIon> {
         match self {
             Self::LinearSemiAmbiguous(p) => Cow::Owned(p.clone().into()),
             Self::LinearSimpleLinear(p) => Cow::Owned(p.clone().into()),
@@ -617,8 +609,8 @@ impl IdentifiedPeptide {
             | MetaData::DeepNovoFamily(_)
             | MetaData::InstaNovo(_)
             | MetaData::PowerNovo(_)
-            | MetaData::PepNet(_)
-            | MetaData::SpectrumSequenceList(_) => None,
+            | MetaData::SpectrumSequenceList(_)
+            | MetaData::PepNet(_) => None,
         }
     }
 
@@ -638,9 +630,9 @@ impl IdentifiedPeptide {
             | MetaData::Fasta(_)
             | MetaData::PowerNovo(_)
             | MetaData::DeepNovoFamily(_)
+            | MetaData::SpectrumSequenceList(_)
             | MetaData::InstaNovo(_)
-            | MetaData::PepNet(_)
-            | MetaData::SpectrumSequenceList(_) => None,
+            | MetaData::PepNet(_) => None,
         }
     }
 
@@ -675,18 +667,19 @@ impl IdentifiedPeptide {
             | MetaData::NovoB(_)
             | MetaData::Fasta(_)
             | MetaData::PowerNovo(_)
-            | MetaData::PepNet(_)
-            | MetaData::SpectrumSequenceList(_) => None,
+            | MetaData::SpectrumSequenceList(_)
+            | MetaData::PepNet(_) => None,
         }
     }
 
-    /// Get the matched fragments, potentially with m/z and intensity
-    pub fn matched_fragments(
-        &self,
-    ) -> Option<Vec<(Option<MassOverCharge>, Option<f64>, Fragment)>> {
-        // OPair, MaxQuant, PLGS
-        None
-    }
+    // Get the matched fragments, potentially with m/z and intensity
+    // #[doc(hidden)]
+    // pub fn matched_fragments(
+    //     &self,
+    // ) -> Option<Vec<(Option<MassOverCharge>, Option<f64>, Fragment)>> {
+    //     // OPair, MaxQuant, PLGS
+    //     None
+    // }
 }
 
 /// Multiple spectrum identifiers
@@ -813,7 +806,7 @@ where
     /// Allow post processing of the peptide
     /// # Errors
     /// On errors in the post processing, format specific
-    #[allow(unused_variables)]
+    #[expect(unused_variables)]
     fn post_process(
         source: &Self::Source,
         parsed: Self,
@@ -845,11 +838,8 @@ pub struct IdentifiedPeptideIter<
     peek: Option<Result<R, CustomError>>,
 }
 
-impl<
-        'lifetime,
-        R: IdentifiedPeptideSource + Clone,
-        I: Iterator<Item = Result<R::Source, CustomError>>,
-    > IdentifiedPeptideIter<'lifetime, R, I>
+impl<R: IdentifiedPeptideSource + Clone, I: Iterator<Item = Result<R::Source, CustomError>>>
+    IdentifiedPeptideIter<'_, R, I>
 where
     R::Format: 'static,
 {
@@ -882,8 +872,8 @@ where
     }
 }
 
-impl<'lifetime, R: IdentifiedPeptideSource, I: Iterator<Item = Result<R::Source, CustomError>>>
-    Iterator for IdentifiedPeptideIter<'lifetime, R, I>
+impl<R: IdentifiedPeptideSource, I: Iterator<Item = Result<R::Source, CustomError>>> Iterator
+    for IdentifiedPeptideIter<'_, R, I>
 where
     R::Format: 'static,
 {
@@ -934,7 +924,7 @@ where
 /// # Errors
 /// * If the peptide was not identified as the correct version of the format (see parameters).
 /// * See errors at``test_identified_peptide()``
-#[allow(clippy::missing_panics_doc)]
+#[expect(clippy::missing_panics_doc)]
 #[cfg(test)]
 pub fn test_format<T: IdentifiedPeptideSource + Into<IdentifiedPeptide>>(
     reader: impl std::io::Read,
@@ -976,7 +966,7 @@ where
 /// * If the score of the peptide is outside of the range -1.0..=1.0.
 /// * If any of the local scores is outside of range -1.0..=1.0.
 /// * If the peptide contains mass modifications (see parameters).
-#[allow(clippy::missing_panics_doc)]
+#[expect(clippy::missing_panics_doc)]
 #[cfg(test)]
 pub fn test_identified_peptide(
     peptide: &IdentifiedPeptide,
@@ -1018,7 +1008,7 @@ pub fn test_identified_peptide(
     }
     if !allow_mass_mods
         && peptide.peptide().is_some_and(|p| {
-            p.compound_peptidoform().peptides().any(|p| {
+            p.compound_peptidoform().peptidoforms().any(|p| {
                 p.sequence().iter().any(|s| {
                     s.modifications.iter().any(|m| {
                         m.simple().is_some_and(|m| {
@@ -1037,8 +1027,8 @@ pub fn test_identified_peptide(
     }
     if let Err(err) = peptide.peptide().map_or(Ok(()), |p| {
         p.compound_peptidoform()
-            .peptides()
-            .try_for_each(LinearPeptide::enforce_modification_rules)
+            .peptidoforms()
+            .try_for_each(Peptidoform::enforce_modification_rules)
     }) {
         return Err(format!(
             "Peptide {} contains misplaced modifications, sequence {}\n{}",
diff --git a/rustyms/src/identification/instanovo.rs b/rustyms/src/identification/instanovo.rs
index df6bca66..2e325538 100644
--- a/rustyms/src/identification/instanovo.rs
+++ b/rustyms/src/identification/instanovo.rs
@@ -4,7 +4,7 @@ use crate::{
     modification::Ontology,
     ontologies::CustomDatabase,
     system::{usize::Charge, MassOverCharge},
-    LinearPeptide, SemiAmbiguous, SloppyParsingParameters,
+    Peptidoform, SemiAmbiguous, SloppyParsingParameters,
 };
 
 use std::path::{Path, PathBuf};
@@ -36,7 +36,7 @@ format_family!(
         mz: MassOverCharge, |location: Location, _| location.parse::<f64>(NUMBER_ERROR).map(MassOverCharge::new::<crate::system::mz>);
         z: Charge, |location: Location, _| location.parse::<usize>(NUMBER_ERROR).map(Charge::new::<crate::system::e>);
         raw_file: PathBuf, |location: Location, _| Ok(Path::new(&location.get_string()).to_owned());
-        peptide: LinearPeptide<SemiAmbiguous>, |location: Location, custom_database: Option<&CustomDatabase>| LinearPeptide::sloppy_pro_forma(
+        peptide: Peptidoform<SemiAmbiguous>, |location: Location, custom_database: Option<&CustomDatabase>| Peptidoform::sloppy_pro_forma(
             location.full_line(),
             location.location.clone(),
             custom_database,
@@ -88,7 +88,6 @@ pub const INSTANOVO_V1_0_0: InstaNovoFormat = InstaNovoFormat {
 
 /// All possible InstaNovo versions
 #[derive(Clone, Eq, PartialEq, Ord, PartialOrd, Hash, Debug, Default, Serialize, Deserialize)]
-#[allow(non_camel_case_types)]
 pub enum InstaNovoVersion {
     #[default]
     /// InstaNovo version 1.0.0
diff --git a/rustyms/src/identification/maxquant.rs b/rustyms/src/identification/maxquant.rs
index 7a959f98..1495d18f 100644
--- a/rustyms/src/identification/maxquant.rs
+++ b/rustyms/src/identification/maxquant.rs
@@ -3,9 +3,9 @@ use std::path::{Path, PathBuf};
 use crate::{
     error::CustomError,
     ontologies::CustomDatabase,
-    peptide::{SemiAmbiguous, SloppyParsingParameters},
+    peptidoform::{SemiAmbiguous, SloppyParsingParameters},
     system::{usize::Charge, Mass, MassOverCharge, Time},
-    LinearPeptide,
+    Peptidoform,
 };
 use serde::{Deserialize, Serialize};
 
@@ -34,7 +34,7 @@ format_family!(
         scan: Vec<usize>, |location: Location, _| location.or_empty().array(';').map(|s| s.parse(NUMBER_ERROR)).collect::<Result<Vec<usize>, CustomError>>();
         modifications: String, |location: Location, _| Ok(location.get_string());
         proteins: String, |location: Location, _| Ok(location.get_string());
-        peptide: Option<LinearPeptide<SemiAmbiguous>>, |location: Location, custom_database: Option<&CustomDatabase>| location.or_empty().parse_with(|location| LinearPeptide::sloppy_pro_forma(
+        peptide: Option<Peptidoform<SemiAmbiguous>>, |location: Location, custom_database: Option<&CustomDatabase>| location.or_empty().parse_with(|location| Peptidoform::sloppy_pro_forma(
             location.full_line(),
             location.location.clone(),
             custom_database,
@@ -47,9 +47,9 @@ format_family!(
     }
     optional {
         raw_file: PathBuf, |location: Location, _| Ok(Path::new(&location.get_string()).to_owned());
-        all_modified_sequences: Vec<LinearPeptide<SemiAmbiguous>>, |location: Location, custom_database: Option<&CustomDatabase>| location.array(';')
-                .map(|s| LinearPeptide::sloppy_pro_forma(s.line.line(), s.location, custom_database, &SloppyParsingParameters::default()))
-                .collect::<Result<Vec<LinearPeptide<SemiAmbiguous>>, CustomError>>();
+        all_modified_sequences: Vec<Peptidoform<SemiAmbiguous>>, |location: Location, custom_database: Option<&CustomDatabase>| location.array(';')
+                .map(|s| Peptidoform::sloppy_pro_forma(s.line.line(), s.location, custom_database, &SloppyParsingParameters::default()))
+                .collect::<Result<Vec<Peptidoform<SemiAmbiguous>>, CustomError>>();
         base_peak_intensity: f64, |location: Location, _| location.parse::<f64>(NUMBER_ERROR);
         carbamidomethyl_c_probabilities: String, |location: Location, _| Ok(location.get_string());
         carbamidomethyl_c_score_differences: String, |location: Location, _| Ok(location.get_string());
@@ -117,7 +117,7 @@ impl From<MaxQuantData> for IdentifiedPeptide {
 pub enum MaxQuantVersion {
     /// msms.txt
     #[default]
-    #[allow(clippy::upper_case_acronyms)]
+    #[expect(clippy::upper_case_acronyms)]
     MSMS,
     /// msmsScans.txt
     MSMSScans,
diff --git a/rustyms/src/identification/msfragger.rs b/rustyms/src/identification/msfragger.rs
index b7efd8f5..744467c5 100644
--- a/rustyms/src/identification/msfragger.rs
+++ b/rustyms/src/identification/msfragger.rs
@@ -6,9 +6,9 @@ use crate::{
     helper_functions::explain_number_error,
     identification::SpectrumId,
     ontologies::CustomDatabase,
-    peptide::{SemiAmbiguous, SloppyParsingParameters},
+    peptidoform::{SemiAmbiguous, SloppyParsingParameters},
     system::{usize::Charge, Mass, MassOverCharge, Time},
-    LinearPeptide,
+    Peptidoform,
 };
 use itertools::Itertools;
 use serde::{Deserialize, Serialize};
@@ -42,14 +42,14 @@ format_family!(
     required {
         scan: SpectrumId, |location: Location, _| Ok(SpectrumId::Native(location.get_string()));
         spectrum_file: PathBuf, |location: Location, _| Ok(location.get_string().into());
-        peptide: Option<LinearPeptide<SemiAmbiguous>>, |location: Location, custom_database: Option<&CustomDatabase>| location.or_empty().parse_with(|location| LinearPeptide::sloppy_pro_forma(
+        peptide: Option<Peptidoform<SemiAmbiguous>>, |location: Location, custom_database: Option<&CustomDatabase>| location.or_empty().parse_with(|location| Peptidoform::sloppy_pro_forma(
             location.full_line(),
             location.location.clone(),
             custom_database,
             &SloppyParsingParameters {ignore_prefix_lowercase_n: true, ..Default::default()},
         ));
-        extended_peptide: Box<[Option<LinearPeptide<SemiAmbiguous>>; 3]>, |location: Location, custom_database: Option<&CustomDatabase>| {
-            let peptides = location.clone().array('.').map(|l| l.or_empty().parse_with(|location| LinearPeptide::sloppy_pro_forma(
+        extended_peptide: Box<[Option<Peptidoform<SemiAmbiguous>>; 3]>, |location: Location, custom_database: Option<&CustomDatabase>| {
+            let peptides = location.clone().array('.').map(|l| l.or_empty().parse_with(|location| Peptidoform::sloppy_pro_forma(
                 location.full_line(),
                 location.location.clone(),
                 custom_database,
@@ -131,7 +131,6 @@ impl From<MSFraggerData> for IdentifiedPeptide {
 pub enum MSFraggerVersion {
     /// Version 21
     #[default]
-    #[allow(clippy::upper_case_acronyms)]
     V21,
     /// Version 22
     V22,
diff --git a/rustyms/src/identification/mztab.rs b/rustyms/src/identification/mztab.rs
index ecdbc7d7..48588160 100644
--- a/rustyms/src/identification/mztab.rs
+++ b/rustyms/src/identification/mztab.rs
@@ -17,7 +17,7 @@ use crate::{
     modification::SimpleModification,
     ontologies::CustomDatabase,
     system::{usize::Charge, MassOverCharge, Time},
-    AminoAcid, LinearPeptide, PeptideModificationSearch, ReturnModification, SemiAmbiguous,
+    AminoAcid, PeptideModificationSearch, Peptidoform, ReturnModification, SemiAmbiguous,
     SloppyParsingParameters, Tolerance,
 };
 
@@ -27,7 +27,7 @@ use super::modification::SimpleModificationInner;
 #[derive(Clone, PartialEq, Debug, Default, Serialize, Deserialize)]
 pub struct MZTabData {
     /// The peptide's sequence corresponding to the PSM
-    pub peptide: Option<LinearPeptide<SemiAmbiguous>>,
+    pub peptide: Option<Peptidoform<SemiAmbiguous>>,
     /// A unique identifier for a PSM within the file. If a PSM can be matched to
     /// multiple proteins, the same PSM should be represented on multiple rows with
     /// different accessions and the same PSM_ID.
@@ -120,7 +120,7 @@ impl MZTabData {
                                 match CVTerm::from_str(&line[fields[2].clone()]).and_then(|term|
                                         (term.id.trim() != "MS:1002453" && term.id.trim()  != "MS:1002454").then(||
                                             SimpleModificationInner::try_from(term.id.trim(), 0..term.id.trim().len(), &mut Vec::new(), &mut Vec::new(), custom_database)).transpose()) {
-                                    Ok(Some(ReturnModification::Defined(modification))) => if !modifications.contains(&modification) { modifications.push(modification)},
+                                    Ok(Some((ReturnModification::Defined(modification), _))) => if !modifications.contains(&modification) { modifications.push(modification)},
                                     Ok(Some(_)) => return Some(Err(CustomError::error("Invalid modification in mzTab", "Modifications in mzTab have to be defeined, not ambiguous or cross-linkers", Context::line_range(Some(line_index), line, fields[2].clone())))),
                                     Err(err) => return Some(Err(err)),
                                     Ok(None) => (),
@@ -263,7 +263,7 @@ impl MZTabData {
     /// Parse a single PSM line
     /// # Errors
     /// When not in the correct format
-    #[allow(clippy::missing_panics_doc)]
+    #[expect(clippy::missing_panics_doc)]
     fn from_line(
         line: PSMLine<'_>,
         global_modifications: &[SimpleModification],
@@ -289,7 +289,7 @@ impl MZTabData {
                         mod_index+1+pos.len()..mod_index+definition.len(),
                         &mut Vec::new(),
                         &mut Vec::new(),
-                        custom_database)?.defined()
+                        custom_database)?.0.defined()
                         .ok_or_else(
                             || CustomError::error(
                                 "Invalid modification",
@@ -305,14 +305,14 @@ impl MZTabData {
             })
             .collect::<Result<Vec<_>, CustomError>>()?;
 
-        Ok(Self {
+        let mut result = Self {
             peptide: {
                 let range = line.required_column("sequence")?.1;
 
                 if range.is_empty() {
                     None
                 } else {
-                    let mut peptide = LinearPeptide::sloppy_pro_forma(
+                    let mut peptide = Peptidoform::sloppy_pro_forma(
                         line.line,
                         range,
                         custom_database,
@@ -323,9 +323,9 @@ impl MZTabData {
                     )?;
                     for (location, modification) in modifications {
                         match location {
-                            0 => peptide.set_simple_n_term(Some(modification)),
+                            0 => peptide.add_simple_n_term(modification),
                             c if c == peptide.len() + 1 => {
-                                peptide.set_simple_c_term(Some(modification));
+                                peptide.add_simple_c_term(modification);
                             }
                             i => {
                                 peptide.sequence_mut()[i - 1].add_simple_modification(modification);
@@ -352,20 +352,20 @@ impl MZTabData {
             })?,
             accession: line
                 .optional_column("accession")
-                .and_then(|(v, _)| (v.to_ascii_lowercase() != "null").then(|| v.to_string())),
+                .and_then(|(v, _)| (!v.eq_ignore_ascii_case("null")).then(|| v.to_string())),
             unique: line
                 .optional_column("unique")
-                .and_then(|(v, _)| (v.to_ascii_lowercase() != "null").then(|| v == "1")),
+                .and_then(|(v, _)| (!v.eq_ignore_ascii_case("null")).then(|| v == "1")),
             database: line
                 .optional_column("database")
-                .and_then(|(v, _)| (v.to_ascii_lowercase() != "null").then(|| v.to_string())),
+                .and_then(|(v, _)| (!v.eq_ignore_ascii_case("null")).then(|| v.to_string())),
             database_version: line
                 .optional_column("database_version")
-                .and_then(|(v, _)| (v.to_ascii_lowercase() != "null").then(|| v.to_string())),
+                .and_then(|(v, _)| (!v.eq_ignore_ascii_case("null")).then(|| v.to_string())),
             search_engine: {
                 let (value, range) = line.required_column("search_engine")?;
 
-                if value.trim().to_ascii_lowercase() == "null" {
+                if value.trim().eq_ignore_ascii_case("null") {
                     Vec::new()
                 } else {
                     value
@@ -374,7 +374,7 @@ impl MZTabData {
                         .map(|(i, s)| {
                             line.optional_column(&format!("search_engine_score[{}]", i + 1))
                                 .and_then(|(v, _)| {
-                                    (v.to_ascii_lowercase() != "null").then(|| {
+                                    (!v.eq_ignore_ascii_case("null")).then(|| {
                                         v.parse::<f64>().map_err(|err| {
                                             CustomError::error(
                                                 "Invalid mzTab search engine score",
@@ -431,7 +431,7 @@ impl MZTabData {
             rt: line
                 .optional_column("retention_time")
                 .and_then(|(v, r)| {
-                    (v.to_ascii_lowercase() != "null").then(|| {
+                    (!v.eq_ignore_ascii_case("null")).then(|| {
                         v.parse::<f64>()
                             .map_err(|err| {
                                 CustomError::error(
@@ -447,7 +447,7 @@ impl MZTabData {
             z: {
                 let (value, range) = line.required_column("charge")?;
 
-                if value.trim().to_ascii_lowercase() == "null" {
+                if value.trim().eq_ignore_ascii_case("null") {
                     Charge::new::<crate::system::e>(1)
                 } else {
                     value
@@ -466,7 +466,7 @@ impl MZTabData {
             mz: line
                 .optional_column("exp_mass_to_charge")
                 .and_then(|(v, r)| {
-                    (v.to_ascii_lowercase() != "null").then(|| {
+                    (!v.eq_ignore_ascii_case("null")).then(|| {
                         v.parse::<f64>()
                             .map_err(|err| {
                                 CustomError::error(
@@ -571,7 +571,7 @@ impl MZTabData {
             start: line
                 .optional_column("start")
                 .and_then(|(v, r)| {
-                    (v.to_ascii_lowercase() != "null").then(|| {
+                    (!v.eq_ignore_ascii_case("null")).then(|| {
                         v.parse::<usize>().map_err(|err| {
                             CustomError::error(
                                 "Invalid mzTab start",
@@ -585,7 +585,7 @@ impl MZTabData {
             end: line
                 .optional_column("end")
                 .and_then(|(v, r)| {
-                    (v.to_ascii_lowercase() != "null").then(|| {
+                    (!v.eq_ignore_ascii_case("null")).then(|| {
                         v.parse::<usize>().map_err(|err| {
                             CustomError::error(
                                 "Invalid mzTab end",
@@ -631,7 +631,19 @@ impl MZTabData {
                     )
                 })
                 .collect(),
-        })
+        };
+
+        result.local_confidence = result.local_confidence.as_ref().map(|lc| {
+            // Casanovo stores the confidence for N and C terminal modifications
+            // As Casanovo has a double N terminal modification (+43.006-17.027) which could also
+            // exist as two separate modifications the number of N terminal modifications is not a
+            // reliable measure to detrmine how many local confidence scores to ignore.
+            let c = result.peptide.as_ref().map_or(0, |p| p.get_c_term().len());
+            let n = lc.len() - c - result.peptide.as_ref().map_or(0, Peptidoform::len);
+            lc[n..lc.len() - c].to_vec()
+        });
+
+        Ok(result)
     }
 }
 
@@ -700,15 +712,17 @@ impl<'a> PSMLine<'a> {
 impl From<MZTabData> for IdentifiedPeptide {
     fn from(value: MZTabData) -> Self {
         Self {
-            score: value.search_engine.is_empty().then(|| {
-                (value
-                    .search_engine
-                    .iter()
-                    .filter_map(|(_, s, _)| *s)
-                    .sum::<f64>()
-                    / value.search_engine.len() as f64)
-                    .clamp(-1.0, 1.0)
-            }),
+            score: (!value.search_engine.is_empty())
+                .then(|| {
+                    (value
+                        .search_engine
+                        .iter()
+                        .filter_map(|(_, s, _)| *s)
+                        .sum::<f64>()
+                        / value.search_engine.len() as f64)
+                        .clamp(-1.0, 1.0)
+                })
+                .filter(|v| !v.is_nan()),
             local_confidence: value.local_confidence.clone(),
             metadata: MetaData::MZTab(value),
         }
@@ -785,7 +799,7 @@ impl std::str::FromStr for CVTerm {
 }
 
 /// The reliability of a PSM
-#[allow(missing_docs)]
+#[expect(missing_docs)]
 #[derive(Clone, PartialEq, Eq, Debug, Default, Serialize, Deserialize)]
 pub enum PSMReliability {
     High,
@@ -805,7 +819,7 @@ impl std::fmt::Display for PSMReliability {
 }
 
 /// A basic structure for a mzTab file line
-#[allow(clippy::upper_case_acronyms)]
+#[expect(clippy::upper_case_acronyms)]
 enum MZTabLine {
     /// Metadata line
     MTD(usize, String, Vec<Range<usize>>),
diff --git a/rustyms/src/identification/mztab_test.rs b/rustyms/src/identification/mztab_test.rs
index 0c75dded..9a07d44d 100644
--- a/rustyms/src/identification/mztab_test.rs
+++ b/rustyms/src/identification/mztab_test.rs
@@ -77,7 +77,7 @@ fn casanovo_v4_2_1() {
 fn contranovo_v1_0_0() {
     assert_eq!(
         open_file(BufReader::new(CONTRANOVO_V1_0_0.as_bytes())).unwrap(),
-        18
+        20
     );
 }
 
diff --git a/rustyms/src/identification/novob.rs b/rustyms/src/identification/novob.rs
index 9c42433d..2af43e8b 100644
--- a/rustyms/src/identification/novob.rs
+++ b/rustyms/src/identification/novob.rs
@@ -5,7 +5,7 @@ use crate::{
     ontologies::CustomDatabase,
     system::Ratio,
     system::{usize::Charge, Mass},
-    AminoAcid, LinearPeptide, SemiAmbiguous, SloppyParsingParameters,
+    AminoAcid, Peptidoform, SemiAmbiguous, SloppyParsingParameters,
 };
 
 use serde::{Deserialize, Serialize};
@@ -26,7 +26,7 @@ static NUMBER_ERROR: (&str, &str) = (
 static PARAMETERS_LOCK: OnceLock<SloppyParsingParameters> = OnceLock::new();
 
 /// Global parsing parameters
-#[allow(clippy::missing_panics_doc)] // These modifications exist
+#[expect(clippy::missing_panics_doc)] // These modifications exist
 fn parameters() -> &'static SloppyParsingParameters {
     PARAMETERS_LOCK.get_or_init(|| SloppyParsingParameters {
         custom_alphabet: vec![
@@ -94,8 +94,8 @@ format_family!(
 
         score_forward: f64, |location: Location, _| location.parse::<f64>(NUMBER_ERROR);
         ppm_diff_forward: Ratio, |location: Location, _| location.parse::<f64>(NUMBER_ERROR).map(Ratio::new::<crate::system::ratio::ppm>);
-        peptide_forward: Option<LinearPeptide<SemiAmbiguous>>, |location: Location, custom_database: Option<&CustomDatabase>|
-            location.trim_start_matches("['").trim_end_matches("']").or_empty().map(|location| LinearPeptide::sloppy_pro_forma(
+        peptide_forward: Option<Peptidoform<SemiAmbiguous>>, |location: Location, custom_database: Option<&CustomDatabase>|
+            location.trim_start_matches("['").trim_end_matches("']").or_empty().map(|location| Peptidoform::sloppy_pro_forma(
                 location.full_line(),
                 location.location.clone(),
                 custom_database,
@@ -104,8 +104,8 @@ format_family!(
 
         score_reverse: f64, |location: Location, _| location.parse::<f64>(NUMBER_ERROR);
         ppm_diff_reverse: Ratio, |location: Location, _| location.parse::<f64>(NUMBER_ERROR).map(Ratio::new::<crate::system::ratio::ppm>);
-        peptide_reverse: Option<LinearPeptide<SemiAmbiguous>>, | location: Location, custom_database: Option<&CustomDatabase>|
-            location.trim_start_matches("['").trim_end_matches("']").or_empty().map(|location| LinearPeptide::sloppy_pro_forma(
+        peptide_reverse: Option<Peptidoform<SemiAmbiguous>>, | location: Location, custom_database: Option<&CustomDatabase>|
+            location.trim_start_matches("['").trim_end_matches("']").or_empty().map(|location| Peptidoform::sloppy_pro_forma(
                 location.full_line(),
                 location.location.clone(),
                 custom_database,
@@ -143,7 +143,6 @@ pub const NOVOB_V0_0_1: NovoBFormat = NovoBFormat {
 
 /// All possible NovoB versions
 #[derive(Clone, Eq, PartialEq, Ord, PartialOrd, Hash, Debug, Default, Serialize, Deserialize)]
-#[allow(non_camel_case_types)]
 pub enum NovoBVersion {
     #[default]
     /// NovoB version 0.0.1
diff --git a/rustyms/src/identification/novor.rs b/rustyms/src/identification/novor.rs
index 4aac44ff..17f0c35e 100644
--- a/rustyms/src/identification/novor.rs
+++ b/rustyms/src/identification/novor.rs
@@ -6,9 +6,9 @@ use super::{
 use crate::{
     error::CustomError,
     ontologies::CustomDatabase,
-    peptide::{SemiAmbiguous, SloppyParsingParameters},
+    peptidoform::{SemiAmbiguous, SloppyParsingParameters},
     system::{usize::Charge, Mass, MassOverCharge, Time},
-    LinearPeptide,
+    Peptidoform,
 };
 use serde::{Deserialize, Serialize};
 
@@ -29,7 +29,7 @@ format_family!(
         z: Charge, |location: Location, _| location.parse::<usize>(NUMBER_ERROR).map(Charge::new::<crate::system::e>);
         mass: Mass, |location: Location, _| location.parse::<f64>(NUMBER_ERROR).map(Mass::new::<crate::system::dalton>);
         score: f64, |location: Location, _| location.parse::<f64>(NUMBER_ERROR);
-        peptide: LinearPeptide<SemiAmbiguous>, |location: Location, custom_database: Option<&CustomDatabase>| LinearPeptide::sloppy_pro_forma(
+        peptide: Peptidoform<SemiAmbiguous>, |location: Location, custom_database: Option<&CustomDatabase>| Peptidoform::sloppy_pro_forma(
             location.full_line(),
             location.location.clone(),
             custom_database,
diff --git a/rustyms/src/identification/opair.rs b/rustyms/src/identification/opair.rs
index 7ae954bb..329a4e9e 100644
--- a/rustyms/src/identification/opair.rs
+++ b/rustyms/src/identification/opair.rs
@@ -12,9 +12,9 @@ use super::{
 use crate::{
     error::{Context, CustomError},
     ontologies::CustomDatabase,
-    peptide::{SemiAmbiguous, SloppyParsingParameters},
+    peptidoform::{SemiAmbiguous, SloppyParsingParameters},
     system::{usize::Charge, Mass, MassOverCharge, Time},
-    AminoAcid, LinearPeptide,
+    AminoAcid, Peptidoform,
 };
 use serde::{Deserialize, Serialize};
 
@@ -119,7 +119,7 @@ format_family!(
                 ))
             },
         );
-        peptide: LinearPeptide<SemiAmbiguous>, |location: Location, custom_database: Option<&CustomDatabase>| LinearPeptide::sloppy_pro_forma(
+        peptide: Peptidoform<SemiAmbiguous>, |location: Location, custom_database: Option<&CustomDatabase>| Peptidoform::sloppy_pro_forma(
             location.full_line(),
             location.location.clone(),
             custom_database,
@@ -271,7 +271,7 @@ pub const O_PAIR: OpairFormat = OpairFormat {
 };
 
 #[derive(Clone, Eq, PartialEq, Ord, PartialOrd, Hash, Debug, Default, Serialize, Deserialize)]
-#[allow(missing_docs)]
+#[expect(missing_docs)]
 pub enum OpairMatchKind {
     #[default]
     Decoy,
diff --git a/rustyms/src/identification/peaks.rs b/rustyms/src/identification/peaks.rs
index 4f45dd14..6e87c694 100644
--- a/rustyms/src/identification/peaks.rs
+++ b/rustyms/src/identification/peaks.rs
@@ -4,9 +4,9 @@ use crate::{
     error::CustomError,
     identification::PeaksFamilyId,
     ontologies::CustomDatabase,
-    peptide::{SemiAmbiguous, SloppyParsingParameters},
+    peptidoform::{SemiAmbiguous, SloppyParsingParameters},
     system::{usize::Charge, Mass, MassOverCharge, Time},
-    LinearPeptide,
+    Peptidoform,
 };
 use itertools::Itertools;
 use serde::{Deserialize, Serialize};
@@ -16,7 +16,7 @@ use super::{
     csv::{parse_csv, CsvLine},
     fasta::FastaIdentifier,
     modification::SimpleModification,
-    peptide::PeptideModificationSearch,
+    peptidoform::PeptideModificationSearch,
     BoxedIdentifiedPeptideIter, IdentifiedPeptide, IdentifiedPeptideSource, MetaData, Modification,
 };
 
@@ -36,7 +36,7 @@ format_family!(
     PeaksData,
     PeaksVersion, [&V12, &V11, &V11_FEATURES, &XPLUS, &AB, &X_PATCHED, &X, &DB_PEPTIDE, &DB_PSM, &DB_PROTEIN_PEPTIDE], b',', None;
     required {
-        peptide: (Option<crate::AminoAcid>, Vec<LinearPeptide<SemiAmbiguous>>, Option<crate::AminoAcid>), |location: Location, custom_database: Option<&CustomDatabase>| {
+        peptide: (Option<crate::AminoAcid>, Vec<Peptidoform<SemiAmbiguous>>, Option<crate::AminoAcid>), |location: Location, custom_database: Option<&CustomDatabase>| {
             let n_flanking: Option<crate::AminoAcid> =
                 (location.as_str().chars().nth(1) == Some('.'))
                 .then(|| location.as_str().chars().next().unwrap().try_into().map_err(|()|
@@ -53,7 +53,7 @@ format_family!(
                         "This flanking residue is not a valid amino acid",
                         crate::error::Context::line(Some(location.line.line_index()), location.full_line(), location.location.end-1, location.location.end)))).transpose()?;
             if c_flanking.is_none() && n_flanking.is_none() {
-                location.array(';').map(|l| LinearPeptide::sloppy_pro_forma(
+                location.array(';').map(|l| Peptidoform::sloppy_pro_forma(
                     l.full_line(),
                     l.location.clone(),
                     custom_database,
@@ -62,7 +62,7 @@ format_family!(
                 .collect::<Result<Vec<_>,_>>()
                 .map(|sequences| (n_flanking, sequences, c_flanking))
             } else {
-            LinearPeptide::sloppy_pro_forma(
+            Peptidoform::sloppy_pro_forma(
                 location.full_line(),
                 n_flanking.map_or(location.location.start, |_| location.location.start+2)..c_flanking.map_or(location.location.end, |_| location.location.end-2),
                 custom_database,
@@ -104,7 +104,7 @@ format_family!(
         feature_tryp_cid: usize, |location: Location, _| location.parse(NUMBER_ERROR).map(Some);
         feature_tryp_ead: usize, |location: Location, _| location.parse(NUMBER_ERROR).map(Some);
         id: usize, |location: Location, _| location.parse(NUMBER_ERROR).map(Some);
-        from_chimera: bool, |location: Location, _| Ok(location.get_string().to_ascii_lowercase() == "yes");
+        from_chimera: bool, |location: Location, _| Ok(location.get_string().eq_ignore_ascii_case("yes"));
         unique: bool, |location: Location, _| Ok(location.get_string() == "Y");
         protein_group: usize, |location: Location, _| location.parse(NUMBER_ERROR).map(Some);
         protein_id: usize, |location: Location, _| location.parse(NUMBER_ERROR).map(Some);
@@ -114,6 +114,8 @@ format_family!(
         quality: f64, |location: Location, _| location.parse::<f64>(NUMBER_ERROR);
         rt_begin: Time, |location: Location, _| location.or_empty().parse::<f64>(NUMBER_ERROR).map(|o| o.map(Time::new::<crate::system::time::s>));
         rt_end: Time, |location: Location, _| location.or_empty().parse::<f64>(NUMBER_ERROR).map(|o| o.map(Time::new::<crate::system::time::s>));
+        precursor_id: isize, |location: Location, _| location.parse::<isize>(NUMBER_ERROR);
+        k0_range: std::ops::RangeInclusive<f64>, |location: Location, _| location.split_once('-').map(|(start, end)| Ok(start.parse(NUMBER_ERROR)?..=end.parse(NUMBER_ERROR)?));
     }
 
     fn post_process(_source: &CsvLine, mut parsed: Self, _custom_database: Option<&CustomDatabase>) -> Result<Self, CustomError> {
@@ -188,6 +190,8 @@ pub const X: PeaksFormat = PeaksFormat {
     quality: OptionalColumn::NotAvailable,
     rt_begin: OptionalColumn::NotAvailable,
     rt_end: OptionalColumn::NotAvailable,
+    precursor_id: OptionalColumn::NotAvailable,
+    k0_range: OptionalColumn::NotAvailable,
 };
 /// Version X of PEAKS export (made for build 31 January 2019)
 pub const X_PATCHED: PeaksFormat = PeaksFormat {
@@ -227,6 +231,8 @@ pub const X_PATCHED: PeaksFormat = PeaksFormat {
     quality: OptionalColumn::NotAvailable,
     rt_begin: OptionalColumn::NotAvailable,
     rt_end: OptionalColumn::NotAvailable,
+    precursor_id: OptionalColumn::NotAvailable,
+    k0_range: OptionalColumn::NotAvailable,
 };
 /// Version X+ of PEAKS export (made for build 20 November 2019)
 pub const XPLUS: PeaksFormat = PeaksFormat {
@@ -266,6 +272,8 @@ pub const XPLUS: PeaksFormat = PeaksFormat {
     quality: OptionalColumn::NotAvailable,
     rt_begin: OptionalColumn::NotAvailable,
     rt_end: OptionalColumn::NotAvailable,
+    precursor_id: OptionalColumn::NotAvailable,
+    k0_range: OptionalColumn::NotAvailable,
 };
 /// Version 11 of PEAKS export
 pub const V11: PeaksFormat = PeaksFormat {
@@ -305,6 +313,8 @@ pub const V11: PeaksFormat = PeaksFormat {
     quality: OptionalColumn::NotAvailable,
     rt_begin: OptionalColumn::NotAvailable,
     rt_end: OptionalColumn::NotAvailable,
+    precursor_id: OptionalColumn::Optional("precursor id"),
+    k0_range: OptionalColumn::Optional("1/k0 range"),
 };
 /// Version 11 of PEAKS export
 pub const V11_FEATURES: PeaksFormat = PeaksFormat {
@@ -344,6 +354,8 @@ pub const V11_FEATURES: PeaksFormat = PeaksFormat {
     protein_accession: OptionalColumn::NotAvailable,
     start: OptionalColumn::NotAvailable,
     end: OptionalColumn::NotAvailable,
+    precursor_id: OptionalColumn::NotAvailable,
+    k0_range: OptionalColumn::NotAvailable,
 };
 /// Version 12 of PEAKS export
 pub const V12: PeaksFormat = PeaksFormat {
@@ -383,6 +395,8 @@ pub const V12: PeaksFormat = PeaksFormat {
     quality: OptionalColumn::NotAvailable,
     rt_begin: OptionalColumn::NotAvailable,
     rt_end: OptionalColumn::NotAvailable,
+    precursor_id: OptionalColumn::NotAvailable,
+    k0_range: OptionalColumn::NotAvailable,
 };
 /// Version Ab of PEAKS export
 pub const AB: PeaksFormat = PeaksFormat {
@@ -422,6 +436,8 @@ pub const AB: PeaksFormat = PeaksFormat {
     quality: OptionalColumn::NotAvailable,
     rt_begin: OptionalColumn::NotAvailable,
     rt_end: OptionalColumn::NotAvailable,
+    precursor_id: OptionalColumn::NotAvailable,
+    k0_range: OptionalColumn::NotAvailable,
 };
 /// Version DB peptide of PEAKS export
 pub const DB_PEPTIDE: PeaksFormat = PeaksFormat {
@@ -461,6 +477,8 @@ pub const DB_PEPTIDE: PeaksFormat = PeaksFormat {
     quality: OptionalColumn::NotAvailable,
     rt_begin: OptionalColumn::NotAvailable,
     rt_end: OptionalColumn::NotAvailable,
+    precursor_id: OptionalColumn::NotAvailable,
+    k0_range: OptionalColumn::NotAvailable,
 };
 /// Version DB psm of PEAKS export
 pub const DB_PSM: PeaksFormat = PeaksFormat {
@@ -500,6 +518,8 @@ pub const DB_PSM: PeaksFormat = PeaksFormat {
     quality: OptionalColumn::NotAvailable,
     rt_begin: OptionalColumn::NotAvailable,
     rt_end: OptionalColumn::NotAvailable,
+    precursor_id: OptionalColumn::NotAvailable,
+    k0_range: OptionalColumn::NotAvailable,
 };
 /// Version DB protein peptide of PEAKS export
 /// protein group, protein id, protein accession, unique, start, end,
@@ -540,11 +560,13 @@ pub const DB_PROTEIN_PEPTIDE: PeaksFormat = PeaksFormat {
     quality: OptionalColumn::NotAvailable,
     rt_begin: OptionalColumn::NotAvailable,
     rt_end: OptionalColumn::NotAvailable,
+    precursor_id: OptionalColumn::NotAvailable,
+    k0_range: OptionalColumn::NotAvailable,
 };
 
 /// All possible peaks versions
 #[derive(Clone, Eq, PartialEq, Ord, PartialOrd, Hash, Debug, Default, Serialize, Deserialize)]
-#[allow(clippy::upper_case_acronyms)]
+#[expect(clippy::upper_case_acronyms)]
 pub enum PeaksVersion {
     /// An older version of a PEAKS export
     X,
diff --git a/rustyms/src/identification/pepnet.rs b/rustyms/src/identification/pepnet.rs
index 68bd8c99..db14f62b 100644
--- a/rustyms/src/identification/pepnet.rs
+++ b/rustyms/src/identification/pepnet.rs
@@ -3,7 +3,7 @@ use crate::{
     identification::{IdentifiedPeptide, IdentifiedPeptideSource, MetaData},
     ontologies::CustomDatabase,
     system::Ratio,
-    LinearPeptide, SemiAmbiguous, SloppyParsingParameters,
+    Peptidoform, SemiAmbiguous, SloppyParsingParameters,
 };
 
 use serde::{Deserialize, Serialize};
@@ -26,7 +26,7 @@ format_family!(
     PepNetData,
     PepNetVersion, [&PEPNET_V1_0], b'\t', None;
     required {
-        peptide: LinearPeptide<SemiAmbiguous>, |location: Location, custom_database: Option<&CustomDatabase>| LinearPeptide::sloppy_pro_forma(
+        peptide: Peptidoform<SemiAmbiguous>, |location: Location, custom_database: Option<&CustomDatabase>| Peptidoform::sloppy_pro_forma(
             location.full_line(),
             location.location.clone(),
             custom_database,
@@ -64,7 +64,6 @@ pub const PEPNET_V1_0: PepNetFormat = PepNetFormat {
 
 /// All possible PepNet versions
 #[derive(Clone, Eq, PartialEq, Ord, PartialOrd, Hash, Debug, Default, Serialize, Deserialize)]
-#[allow(non_camel_case_types)]
 pub enum PepNetVersion {
     #[default]
     /// PepNet version 1.0
diff --git a/rustyms/src/identification/plgs.rs b/rustyms/src/identification/plgs.rs
index f80a2b60..12e67a09 100644
--- a/rustyms/src/identification/plgs.rs
+++ b/rustyms/src/identification/plgs.rs
@@ -3,9 +3,9 @@ use crate::{
     helper_functions::explain_number_error,
     modification::SimpleModification,
     ontologies::CustomDatabase,
-    peptide::SimpleLinear,
+    peptidoform::SimpleLinear,
     system::{usize::Charge, Mass, MassOverCharge, Time},
-    AminoAcid, LinearPeptide, Modification, MolecularFormula, NeutralLoss,
+    AminoAcid, Modification, MolecularFormula, NeutralLoss, Peptidoform,
 };
 use serde::{Deserialize, Serialize};
 
@@ -70,7 +70,7 @@ format_family!(
                 };
                 Ok((modification, aa, index))
             }).collect::<Result<Vec<_>,_>>();
-        peptide: LinearPeptide<SimpleLinear>, |location: Location, custom_database: Option<&CustomDatabase>| LinearPeptide::pro_forma(location.as_str(), custom_database).map(|p|p.into_simple_linear().unwrap());
+        peptide: Peptidoform<SimpleLinear>, |location: Location, custom_database: Option<&CustomDatabase>| Peptidoform::pro_forma(location.as_str(), custom_database).map(|p|p.into_simple_linear().unwrap());
         peptide_start: usize, |location: Location, _| location.parse(NUMBER_ERROR);
         peptide_pi: f64, |location: Location, _| location.parse(NUMBER_ERROR);
         peptide_component_id: usize, |location: Location, _| location.parse(NUMBER_ERROR);
@@ -132,7 +132,7 @@ format_family!(
         for (m, aa, index) in &parsed.peptide_modifications {
             if let Some(index) = index {
                 parsed.peptide.add_simple_modification(SequencePosition::Index(*index), m.clone());
-            } else if !parsed.peptide.add_unknown_position_modification(m.clone(), Some(&[PlacementRule::AminoAcid(vec![*aa], crate::placement_rule::Position::Anywhere)]), ..)
+            } else if !parsed.peptide.add_unknown_position_modification(m.clone(), .., &crate::MUPSettings{position: Some(vec![PlacementRule::AminoAcid(vec![*aa], crate::placement_rule::Position::Anywhere)]), .. Default::default()})
             {
                 return Err(CustomError::error(
                     "Modification of unknown position cannot be placed",
@@ -276,7 +276,6 @@ pub const VERSION_3_0: PLGSFormat = PLGSFormat {
 
 /// All possible PLGS versions
 #[derive(Clone, Eq, PartialEq, Ord, PartialOrd, Hash, Debug, Default, Serialize, Deserialize)]
-#[allow(non_camel_case_types)]
 pub enum PLGSVersion {
     /// Current PLGS version
     #[default]
diff --git a/rustyms/src/identification/plink.rs b/rustyms/src/identification/plink.rs
index f3a2d271..37b99feb 100644
--- a/rustyms/src/identification/plink.rs
+++ b/rustyms/src/identification/plink.rs
@@ -16,7 +16,7 @@ use crate::{
     ontologies::CustomDatabase,
     system::{usize::Charge, Mass},
     tolerance::WithinTolerance,
-    CrossLinkName, LinearPeptide, Peptidoform, SequencePosition, SloppyParsingParameters,
+    CrossLinkName, Peptidoform, PeptidoformIon, SequencePosition, SloppyParsingParameters,
     Tolerance,
 };
 use itertools::Itertools;
@@ -46,13 +46,13 @@ format_family!(
         /// MH+ mass
         theoretical_mass: Mass, |location: Location, _| location.parse::<f64>(NUMBER_ERROR).map(Mass::new::<crate::system::dalton>);
         peptide_type: PLinkPeptideType, |location: Location, _| location.parse::<PLinkPeptideType>(TYPE_ERROR);
-        peptidoform: Peptidoform, |location: Location, _| {
+        peptidoform: PeptidoformIon, |location: Location, _| {
             match plink_separate(location.clone(), "peptide")? {
                 (pep1, Some(pos1), Some(pep2), Some(pos2)) => {
-                    let pep1 = LinearPeptide::sloppy_pro_forma(location.full_line(), pep1, None, &SloppyParsingParameters::default())?;
-                    let pep2 = LinearPeptide::sloppy_pro_forma(location.full_line(), pep2, None, &SloppyParsingParameters::default())?;
+                    let pep1 = Peptidoform::sloppy_pro_forma(location.full_line(), pep1, None, &SloppyParsingParameters::default())?;
+                    let pep2 = Peptidoform::sloppy_pro_forma(location.full_line(), pep2, None, &SloppyParsingParameters::default())?;
 
-                    let mut peptidoform = Peptidoform::from_vec(vec![pep1.into(), pep2.into()]).unwrap();
+                    let mut peptidoform = PeptidoformIon::from_vec(vec![pep1.into(), pep2.into()]).unwrap();
                     peptidoform.add_cross_link(
                         (0, SequencePosition::Index(pos1.0.saturating_sub(1))),
                         (1, SequencePosition::Index(pos2.0.saturating_sub(1))),
@@ -62,9 +62,9 @@ format_family!(
                     Ok(peptidoform)
                 }
                 (pep1, Some(pos1), None, Some(pos2)) => {
-                    let pep = LinearPeptide::sloppy_pro_forma(location.full_line(), pep1, None, &SloppyParsingParameters::default())?;
+                    let pep = Peptidoform::sloppy_pro_forma(location.full_line(), pep1, None, &SloppyParsingParameters::default())?;
 
-                    let mut peptidoform = Peptidoform::from_vec(vec![pep.into()]).unwrap();
+                    let mut peptidoform = PeptidoformIon::from_vec(vec![pep.into()]).unwrap();
                     peptidoform.add_cross_link(
                         (0, SequencePosition::Index(pos1.0.saturating_sub(1))),
                         (0, SequencePosition::Index(pos2.0.saturating_sub(1))),
@@ -74,15 +74,15 @@ format_family!(
                     Ok(peptidoform)
                 }
                 (pep1, Some(pos1), None, None) => {
-                    let mut pep = LinearPeptide::sloppy_pro_forma(location.full_line(), pep1, None, &SloppyParsingParameters::default())?;
+                    let mut pep = Peptidoform::sloppy_pro_forma(location.full_line(), pep1, None, &SloppyParsingParameters::default())?;
                     pep[SequencePosition::Index(pos1.0.saturating_sub(1))].modifications.push( SimpleModificationInner::Mass(Mass::default().into()).into());
 
-                    Ok(Peptidoform::from_vec(vec![pep.into()]).unwrap())
+                    Ok(PeptidoformIon::from_vec(vec![pep.into()]).unwrap())
                 }
                 (pep1, None, None, None) => {
-                    let pep = LinearPeptide::sloppy_pro_forma(location.full_line(), pep1, None, &SloppyParsingParameters::default())?;
+                    let pep = Peptidoform::sloppy_pro_forma(location.full_line(), pep1, None, &SloppyParsingParameters::default())?;
 
-                    Ok(Peptidoform::from_vec(vec![pep.into()]).unwrap())
+                    Ok(PeptidoformIon::from_vec(vec![pep.into()]).unwrap())
                 }
                 _ => unreachable!()
             }
@@ -137,11 +137,11 @@ format_family!(
         raw_file: PathBuf, |location: Location, _| Ok(Some(location.get_string().into()));
     }
 
-    #[allow(clippy::similar_names)]
+    #[expect(clippy::similar_names)]
     fn post_process(source: &CsvLine, mut parsed: Self, custom_database: Option<&CustomDatabase>) -> Result<Self, CustomError> {
         // Add all modifications
-        let pep1 = parsed.peptidoform.peptides()[0].len();
-        let pep2 = parsed.peptidoform.peptides().get(1).map_or(0, LinearPeptide::len);
+        let pep1 = parsed.peptidoform.peptidoforms()[0].len();
+        let pep2 = parsed.peptidoform.peptidoforms().get(1).map_or(0, Peptidoform::len);
         for (m, index) in &parsed.ptm {
             let pos = if *index == 0 {
                 (0, SequencePosition::NTerm)
@@ -171,13 +171,13 @@ format_family!(
 
             match pos {
                 (peptide, SequencePosition::NTerm) => {
-                        parsed.peptidoform.peptides_mut()[peptide].set_simple_n_term(Some(m.clone()));
+                        parsed.peptidoform.peptidoforms_mut()[peptide].add_simple_n_term(m.clone());
                 }
                 (peptide, SequencePosition::CTerm) => {
-                    parsed.peptidoform.peptides_mut()[peptide].set_simple_c_term(Some(m.clone()));
+                    parsed.peptidoform.peptidoforms_mut()[peptide].add_simple_c_term(m.clone());
                 }
                 (peptide, index) => {
-                    parsed.peptidoform.peptides_mut()[peptide][index]
+                    parsed.peptidoform.peptidoforms_mut()[peptide][index]
                             .modifications
                             .push(m.clone().into());
                 }
@@ -218,9 +218,9 @@ format_family!(
                 0 => return Err(CustomError::error("Invalid pLink peptide", format!("The correct cross-linker could not be identified with mass {:.3} Da, if a non default cross-linker was used add this as a custom linker modification.", left_over.value), source.full_context())),
                 1 => {
                     // Replace 0 mass mod + determine Nterm or side chain
-                    for p in parsed.peptidoform.peptides_mut() {
-                        let mut n_term = p.get_n_term().cloned();
-                        let mut c_term = p.get_c_term().cloned();
+                    for p in parsed.peptidoform.peptidoforms_mut() {
+                        let mut n_term = p.get_n_term().to_vec();
+                        let mut c_term = p.get_c_term().to_vec();
                         let len = p.len();
 
                         for (seq_index, seq) in p.sequence_mut().iter_mut().enumerate() {
@@ -233,12 +233,12 @@ format_family!(
                                     if name == &CrossLinkName::Name("1".to_string()) {
                                         *linker = fitting[0].clone();
 
-                                        if is_n_term && m.is_possible(&seq_clone, SequencePosition::NTerm).any_possible() && n_term.is_none() {
+                                        if is_n_term && m.is_possible(&seq_clone, SequencePosition::NTerm).any_possible() {
                                             remove = Some(index);
-                                            n_term = Some(m.clone());
-                                        } else if is_c_term && m.is_possible(&seq_clone, SequencePosition::CTerm).any_possible() && c_term.is_none() {
+                                            n_term.push(m.clone());
+                                        } else if is_c_term && m.is_possible(&seq_clone, SequencePosition::CTerm).any_possible() {
                                             remove = Some(index);
-                                            c_term = Some(m.clone());
+                                            c_term.push(m.clone());
                                         }
                                     }
                                 } else if Modification::Simple(Arc::new(SimpleModificationInner::Mass(Mass::default().into()))) == *m {
diff --git a/rustyms/src/identification/powernovo.rs b/rustyms/src/identification/powernovo.rs
index 501a1bdc..b3bfad77 100644
--- a/rustyms/src/identification/powernovo.rs
+++ b/rustyms/src/identification/powernovo.rs
@@ -4,7 +4,7 @@ use crate::{
         common_parser::OptionalColumn, IdentifiedPeptide, IdentifiedPeptideSource, MetaData,
     },
     ontologies::CustomDatabase,
-    LinearPeptide, SemiAmbiguous, SloppyParsingParameters,
+    Peptidoform, SemiAmbiguous, SloppyParsingParameters,
 };
 
 use std::path::{Path, PathBuf};
@@ -30,7 +30,7 @@ format_family!(
     PowerNovoVersion, [&POWERNOVO_V1_0_1], b',', None;
     required {
         title: String, |location: Location, _| Ok(location.get_string());
-        peptide: LinearPeptide<SemiAmbiguous>, |location: Location, custom_database: Option<&CustomDatabase>| LinearPeptide::sloppy_pro_forma(
+        peptide: Peptidoform<SemiAmbiguous>, |location: Location, custom_database: Option<&CustomDatabase>| Peptidoform::sloppy_pro_forma(
             location.full_line(),
             location.location.clone(),
             custom_database,
@@ -84,7 +84,6 @@ pub const POWERNOVO_V1_0_1: PowerNovoFormat = PowerNovoFormat {
 
 /// All possible PowerNovo versions
 #[derive(Clone, Eq, PartialEq, Ord, PartialOrd, Hash, Debug, Default, Serialize, Deserialize)]
-#[allow(non_camel_case_types)]
 pub enum PowerNovoVersion {
     #[default]
     /// PowerNovo version 1.0.1
diff --git a/rustyms/src/identification/sage.rs b/rustyms/src/identification/sage.rs
index ce7704ad..5c5f552b 100644
--- a/rustyms/src/identification/sage.rs
+++ b/rustyms/src/identification/sage.rs
@@ -4,9 +4,9 @@ use crate::{
     error::CustomError,
     identification::SpectrumId,
     ontologies::CustomDatabase,
-    peptide::SemiAmbiguous,
+    peptidoform::SemiAmbiguous,
     system::{usize::Charge, Mass, Ratio, Time},
-    LinearPeptide,
+    Peptidoform,
 };
 use itertools::Itertools;
 use serde::{Deserialize, Serialize};
@@ -49,7 +49,7 @@ format_family!(
         ms2_intensity: f64, |location: Location, _| location.parse(NUMBER_ERROR);
         scan: SpectrumId, |location: Location, _|Ok(SpectrumId::Native(location.get_string()));
         peptide_q: f64, |location: Location, _| location.parse(NUMBER_ERROR);
-        peptide: LinearPeptide<SemiAmbiguous>, |location: Location, custom_database: Option<&CustomDatabase>| LinearPeptide::pro_forma(location.as_str(), custom_database).map(|p|p.into_semi_ambiguous().unwrap());
+        peptide: Peptidoform<SemiAmbiguous>, |location: Location, custom_database: Option<&CustomDatabase>| Peptidoform::pro_forma(location.as_str(), custom_database).map(|p|p.into_semi_ambiguous().unwrap());
         poisson: f64, |location: Location, _| location.parse(NUMBER_ERROR);
         posterior_error: f64, |location: Location, _| location.parse(NUMBER_ERROR);
         predicted_mobility: f64, |location: Location, _| location.parse(NUMBER_ERROR);
@@ -124,7 +124,6 @@ pub const VERSION_0_14: SageFormat = SageFormat {
 
 /// All possible Sage versions
 #[derive(Clone, Eq, PartialEq, Ord, PartialOrd, Hash, Debug, Default, Serialize, Deserialize)]
-#[allow(non_camel_case_types)]
 pub enum SageVersion {
     /// Current sage version
     #[default]
diff --git a/rustyms/src/identification/ssl.rs b/rustyms/src/identification/ssl.rs
index 10c90dcd..2d72c6bc 100644
--- a/rustyms/src/identification/ssl.rs
+++ b/rustyms/src/identification/ssl.rs
@@ -6,7 +6,7 @@ use crate::{
     },
     ontologies::CustomDatabase,
     system::{isize::Charge, MassOverCharge, Time},
-    LinearPeptide, SemiAmbiguous,
+    Peptidoform, SemiAmbiguous,
 };
 
 use std::path::{Path, PathBuf};
@@ -41,7 +41,7 @@ format_family!(
     optional {
         start_time: Time, |location: Location, _| location.parse::<f64>(NUMBER_ERROR).map(Time::new::<crate::system::time::min>);
         end_time: Time, |location: Location, _| location.parse::<f64>(NUMBER_ERROR).map(Time::new::<crate::system::time::min>);
-        peptide: LinearPeptide<SemiAmbiguous>, |location: Location, custom_database: Option<&CustomDatabase>| LinearPeptide::pro_forma(location.as_str(), custom_database).map(|p|p.into_semi_ambiguous().unwrap());
+        peptide: Peptidoform<SemiAmbiguous>, |location: Location, custom_database: Option<&CustomDatabase>| Peptidoform::pro_forma(location.as_str(), custom_database).map(|p|p.into_semi_ambiguous().unwrap());
         score: f64, |location: Location, _| location.parse::<f64>(NUMBER_ERROR);
         score_type: String, |location: Location, _| Ok(location.get_string());
         rt: Time, |location: Location, _| location.parse::<f64>(NUMBER_ERROR).map(Time::new::<crate::system::time::min>);
@@ -90,7 +90,7 @@ pub const SSL: SpectrumSequenceListFormat = SpectrumSequenceListFormat {
 
 /// All possible SpectrumSequenceList versions
 #[derive(Clone, Eq, PartialEq, Ord, PartialOrd, Hash, Debug, Default, Serialize, Deserialize)]
-#[allow(non_camel_case_types)]
+#[expect(clippy::upper_case_acronyms)]
 pub enum SpectrumSequenceListVersion {
     #[default]
     /// SSL file format
diff --git a/rustyms/src/imgt/germlines/African or Cape clawed frog.bin b/rustyms/src/imgt/germlines/African or Cape clawed frog.bin
index a18a8693..0b9e09db 100644
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diff --git a/rustyms/src/imgt/germlines/Alpaca.bin b/rustyms/src/imgt/germlines/Alpaca.bin
index 2ce83030..c7a5de7e 100644
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diff --git a/rustyms/src/imgt/germlines/American mink.bin b/rustyms/src/imgt/germlines/American mink.bin
index 53de36c9..87a15c80 100644
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diff --git a/rustyms/src/imgt/germlines/Arabian camel.bin b/rustyms/src/imgt/germlines/Arabian camel.bin
index 0fda779d..711e0b53 100644
Binary files a/rustyms/src/imgt/germlines/Arabian camel.bin and b/rustyms/src/imgt/germlines/Arabian camel.bin differ
diff --git a/rustyms/src/imgt/germlines/Atlantic cod.bin b/rustyms/src/imgt/germlines/Atlantic cod.bin
index 1dd1b854..e326ec6f 100644
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diff --git a/rustyms/src/imgt/germlines/Atlantic salmon.bin b/rustyms/src/imgt/germlines/Atlantic salmon.bin
index 6bed936e..126d4537 100644
Binary files a/rustyms/src/imgt/germlines/Atlantic salmon.bin and b/rustyms/src/imgt/germlines/Atlantic salmon.bin differ
diff --git a/rustyms/src/imgt/germlines/Bornean orangutan.bin b/rustyms/src/imgt/germlines/Bornean orangutan.bin
index e9eb59bf..db3e6562 100644
Binary files a/rustyms/src/imgt/germlines/Bornean orangutan.bin and b/rustyms/src/imgt/germlines/Bornean orangutan.bin differ
diff --git a/rustyms/src/imgt/germlines/Channel catfish.bin b/rustyms/src/imgt/germlines/Channel catfish.bin
index fa903ef3..56f83b57 100644
Binary files a/rustyms/src/imgt/germlines/Channel catfish.bin and b/rustyms/src/imgt/germlines/Channel catfish.bin differ
diff --git a/rustyms/src/imgt/germlines/Chimpanzee.bin b/rustyms/src/imgt/germlines/Chimpanzee.bin
index a43fa736..e9d76b2d 100644
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diff --git a/rustyms/src/imgt/germlines/Common gibbon.bin b/rustyms/src/imgt/germlines/Common gibbon.bin
index ff2c87d4..609bb805 100644
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diff --git a/rustyms/src/imgt/germlines/Cook's mouse.bin b/rustyms/src/imgt/germlines/Cook's mouse.bin
index 5fb61b6a..8127279e 100644
Binary files a/rustyms/src/imgt/germlines/Cook's mouse.bin and b/rustyms/src/imgt/germlines/Cook's mouse.bin differ
diff --git a/rustyms/src/imgt/germlines/Crab-eating macaque.bin b/rustyms/src/imgt/germlines/Crab-eating macaque.bin
index 251c5637..eef8dddb 100644
Binary files a/rustyms/src/imgt/germlines/Crab-eating macaque.bin and b/rustyms/src/imgt/germlines/Crab-eating macaque.bin differ
diff --git a/rustyms/src/imgt/germlines/Domestic bovine.bin b/rustyms/src/imgt/germlines/Domestic bovine.bin
index 77a24af7..d825bfd9 100644
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diff --git a/rustyms/src/imgt/germlines/Domestic cat.bin b/rustyms/src/imgt/germlines/Domestic cat.bin
index 74b24ffa..dc546732 100644
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diff --git a/rustyms/src/imgt/germlines/Domestic chicken.bin b/rustyms/src/imgt/germlines/Domestic chicken.bin
index c780a41b..96ad06ca 100644
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diff --git a/rustyms/src/imgt/germlines/Domestic dog.bin b/rustyms/src/imgt/germlines/Domestic dog.bin
index 2c7aabc0..de10fe59 100644
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diff --git a/rustyms/src/imgt/germlines/Domestic ferret.bin b/rustyms/src/imgt/germlines/Domestic ferret.bin
index 14f74f16..93711cba 100644
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diff --git a/rustyms/src/imgt/germlines/Domestic goat.bin b/rustyms/src/imgt/germlines/Domestic goat.bin
index 4cac0358..cb71fdbf 100644
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diff --git a/rustyms/src/imgt/germlines/Domestic horse.bin b/rustyms/src/imgt/germlines/Domestic horse.bin
index 2ddf9229..9718209a 100644
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diff --git a/rustyms/src/imgt/germlines/Domestic pig.bin b/rustyms/src/imgt/germlines/Domestic pig.bin
index a7cacc0f..a9d8f640 100644
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diff --git a/rustyms/src/imgt/germlines/Domestic sheep.bin b/rustyms/src/imgt/germlines/Domestic sheep.bin
index 8da2480f..2947ad96 100644
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diff --git a/rustyms/src/imgt/germlines/Eastern European house mouse.bin b/rustyms/src/imgt/germlines/Eastern European house mouse.bin
index cd65333b..ef527f8a 100644
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diff --git a/rustyms/src/imgt/germlines/European rabbit.bin b/rustyms/src/imgt/germlines/European rabbit.bin
index 21edfdd7..cbdc6a21 100644
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diff --git a/rustyms/src/imgt/germlines/Golden hamster.bin b/rustyms/src/imgt/germlines/Golden hamster.bin
new file mode 100644
index 00000000..dbbcadca
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diff --git a/rustyms/src/imgt/germlines/Horn shark.bin b/rustyms/src/imgt/germlines/Horn shark.bin
index 4b914510..5cf83916 100644
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diff --git a/rustyms/src/imgt/germlines/House mouse.bin b/rustyms/src/imgt/germlines/House mouse.bin
index 057d4365..0368554c 100644
Binary files a/rustyms/src/imgt/germlines/House mouse.bin and b/rustyms/src/imgt/germlines/House mouse.bin differ
diff --git a/rustyms/src/imgt/germlines/Human.bin b/rustyms/src/imgt/germlines/Human.bin
index 439da8bb..f7495ffd 100644
Binary files a/rustyms/src/imgt/germlines/Human.bin and b/rustyms/src/imgt/germlines/Human.bin differ
diff --git a/rustyms/src/imgt/germlines/Japanese wild mouse.bin b/rustyms/src/imgt/germlines/Japanese wild mouse.bin
index 6d31db43..9fd31fb0 100644
Binary files a/rustyms/src/imgt/germlines/Japanese wild mouse.bin and b/rustyms/src/imgt/germlines/Japanese wild mouse.bin differ
diff --git a/rustyms/src/imgt/germlines/Liontail macaque.bin b/rustyms/src/imgt/germlines/Liontail macaque.bin
index d5dd9b6f..ee20c6c0 100644
Binary files a/rustyms/src/imgt/germlines/Liontail macaque.bin and b/rustyms/src/imgt/germlines/Liontail macaque.bin differ
diff --git a/rustyms/src/imgt/germlines/Little skate.bin b/rustyms/src/imgt/germlines/Little skate.bin
index 12f92ba9..21434e16 100644
Binary files a/rustyms/src/imgt/germlines/Little skate.bin and b/rustyms/src/imgt/germlines/Little skate.bin differ
diff --git a/rustyms/src/imgt/germlines/Mice.bin b/rustyms/src/imgt/germlines/Mice.bin
index 18e47987..678576cc 100644
Binary files a/rustyms/src/imgt/germlines/Mice.bin and b/rustyms/src/imgt/germlines/Mice.bin differ
diff --git a/rustyms/src/imgt/germlines/Norway rat.bin b/rustyms/src/imgt/germlines/Norway rat.bin
index 41f23f7c..335a9264 100644
Binary files a/rustyms/src/imgt/germlines/Norway rat.bin and b/rustyms/src/imgt/germlines/Norway rat.bin differ
diff --git a/rustyms/src/imgt/germlines/Olive baboon anubis.bin b/rustyms/src/imgt/germlines/Olive baboon anubis.bin
index 43ab718b..ed689bff 100644
Binary files a/rustyms/src/imgt/germlines/Olive baboon anubis.bin and b/rustyms/src/imgt/germlines/Olive baboon anubis.bin differ
diff --git a/rustyms/src/imgt/germlines/Pere David's macaque.bin b/rustyms/src/imgt/germlines/Pere David's macaque.bin
index 7c1ca71d..08c1bfb3 100644
Binary files a/rustyms/src/imgt/germlines/Pere David's macaque.bin and b/rustyms/src/imgt/germlines/Pere David's macaque.bin differ
diff --git a/rustyms/src/imgt/germlines/Pig-tailed macaque.bin b/rustyms/src/imgt/germlines/Pig-tailed macaque.bin
index 881f36e2..dcb88aa1 100644
Binary files a/rustyms/src/imgt/germlines/Pig-tailed macaque.bin and b/rustyms/src/imgt/germlines/Pig-tailed macaque.bin differ
diff --git a/rustyms/src/imgt/germlines/Platypus.bin b/rustyms/src/imgt/germlines/Platypus.bin
index 3018d3b8..ff603016 100644
Binary files a/rustyms/src/imgt/germlines/Platypus.bin and b/rustyms/src/imgt/germlines/Platypus.bin differ
diff --git a/rustyms/src/imgt/germlines/Rabbit.bin b/rustyms/src/imgt/germlines/Rabbit.bin
index fba12ad1..afe242cf 100644
Binary files a/rustyms/src/imgt/germlines/Rabbit.bin and b/rustyms/src/imgt/germlines/Rabbit.bin differ
diff --git a/rustyms/src/imgt/germlines/Rainbow trout.bin b/rustyms/src/imgt/germlines/Rainbow trout.bin
index 74325b75..a2924d06 100644
Binary files a/rustyms/src/imgt/germlines/Rainbow trout.bin and b/rustyms/src/imgt/germlines/Rainbow trout.bin differ
diff --git a/rustyms/src/imgt/germlines/Rhesus monkey.bin b/rustyms/src/imgt/germlines/Rhesus monkey.bin
index 3b18cc52..bbc669bc 100644
Binary files a/rustyms/src/imgt/germlines/Rhesus monkey.bin and b/rustyms/src/imgt/germlines/Rhesus monkey.bin differ
diff --git a/rustyms/src/imgt/germlines/Ring-tailed lemur.bin b/rustyms/src/imgt/germlines/Ring-tailed lemur.bin
index d5b6d533..3fced046 100644
Binary files a/rustyms/src/imgt/germlines/Ring-tailed lemur.bin and b/rustyms/src/imgt/germlines/Ring-tailed lemur.bin differ
diff --git a/rustyms/src/imgt/germlines/Shrew mouse.bin b/rustyms/src/imgt/germlines/Shrew mouse.bin
index 879588fd..fb90a3be 100644
Binary files a/rustyms/src/imgt/germlines/Shrew mouse.bin and b/rustyms/src/imgt/germlines/Shrew mouse.bin differ
diff --git a/rustyms/src/imgt/germlines/Sooty mangabey.bin b/rustyms/src/imgt/germlines/Sooty mangabey.bin
index 032946bf..ff0dcb8e 100644
Binary files a/rustyms/src/imgt/germlines/Sooty mangabey.bin and b/rustyms/src/imgt/germlines/Sooty mangabey.bin differ
diff --git a/rustyms/src/imgt/germlines/Southeastern Asian house mouse.bin b/rustyms/src/imgt/germlines/Southeastern Asian house mouse.bin
index 4d71c6ef..31a70a86 100644
Binary files a/rustyms/src/imgt/germlines/Southeastern Asian house mouse.bin and b/rustyms/src/imgt/germlines/Southeastern Asian house mouse.bin differ
diff --git a/rustyms/src/imgt/germlines/Southern African pygmy mouse.bin b/rustyms/src/imgt/germlines/Southern African pygmy mouse.bin
index 42477da8..5141fde4 100644
Binary files a/rustyms/src/imgt/germlines/Southern African pygmy mouse.bin and b/rustyms/src/imgt/germlines/Southern African pygmy mouse.bin differ
diff --git a/rustyms/src/imgt/germlines/Spiny mouse.bin b/rustyms/src/imgt/germlines/Spiny mouse.bin
index 062217a6..5721103e 100644
Binary files a/rustyms/src/imgt/germlines/Spiny mouse.bin and b/rustyms/src/imgt/germlines/Spiny mouse.bin differ
diff --git a/rustyms/src/imgt/germlines/Stump-tailed macaque.bin b/rustyms/src/imgt/germlines/Stump-tailed macaque.bin
index 295eeef1..1773051a 100644
Binary files a/rustyms/src/imgt/germlines/Stump-tailed macaque.bin and b/rustyms/src/imgt/germlines/Stump-tailed macaque.bin differ
diff --git a/rustyms/src/imgt/germlines/Sumatran orangutan.bin b/rustyms/src/imgt/germlines/Sumatran orangutan.bin
index 8a80b6ac..321b1f15 100644
Binary files a/rustyms/src/imgt/germlines/Sumatran orangutan.bin and b/rustyms/src/imgt/germlines/Sumatran orangutan.bin differ
diff --git a/rustyms/src/imgt/germlines/Taiwan macaque.bin b/rustyms/src/imgt/germlines/Taiwan macaque.bin
index 004bff13..d8f55a0a 100644
Binary files a/rustyms/src/imgt/germlines/Taiwan macaque.bin and b/rustyms/src/imgt/germlines/Taiwan macaque.bin differ
diff --git a/rustyms/src/imgt/germlines/Western European house mouse.bin b/rustyms/src/imgt/germlines/Western European house mouse.bin
index e5784170..df960f3b 100644
Binary files a/rustyms/src/imgt/germlines/Western European house mouse.bin and b/rustyms/src/imgt/germlines/Western European house mouse.bin differ
diff --git a/rustyms/src/imgt/germlines/Western gorilla.bin b/rustyms/src/imgt/germlines/Western gorilla.bin
index 10263eb6..f78f39c0 100644
Binary files a/rustyms/src/imgt/germlines/Western gorilla.bin and b/rustyms/src/imgt/germlines/Western gorilla.bin differ
diff --git a/rustyms/src/imgt/germlines/Western lowland gorilla.bin b/rustyms/src/imgt/germlines/Western lowland gorilla.bin
index c8ba977d..43a2ce8f 100644
Binary files a/rustyms/src/imgt/germlines/Western lowland gorilla.bin and b/rustyms/src/imgt/germlines/Western lowland gorilla.bin differ
diff --git a/rustyms/src/imgt/germlines/Western wild mouse.bin b/rustyms/src/imgt/germlines/Western wild mouse.bin
index a5317e5e..87f27a84 100644
Binary files a/rustyms/src/imgt/germlines/Western wild mouse.bin and b/rustyms/src/imgt/germlines/Western wild mouse.bin differ
diff --git a/rustyms/src/imgt/germlines/Zebrafish.bin b/rustyms/src/imgt/germlines/Zebrafish.bin
index 8a2593f8..cf0086ec 100644
Binary files a/rustyms/src/imgt/germlines/Zebrafish.bin and b/rustyms/src/imgt/germlines/Zebrafish.bin differ
diff --git a/rustyms/src/imgt/germlines/germlines.md b/rustyms/src/imgt/germlines/germlines.md
index 9d6a1bd1..80852808 100644
--- a/rustyms/src/imgt/germlines/germlines.md
+++ b/rustyms/src/imgt/germlines/germlines.md
@@ -222,7 +222,7 @@ _Number of genes / number of alleles_
 
 | Kind | V | J | C |
 |------|---|---|---|
-|IGHV|81/321|9/19|12/94|
+|IGHV|81/319|9/19|12/94|
 |IGKV|62/109|5/7|1/4|
 |IGLV|51/113|7/10|7/14|
 |IGIV|0/0|0/0|0/0|
@@ -361,6 +361,17 @@ _Number of genes / number of alleles_
 
 _Number of genes / number of alleles_
 
+## Mesocricetus auratus / Golden hamster
+
+| Kind | V | J | C |
+|------|---|---|---|
+|IGHV|0/0|0/0|7/7|
+|IGKV|0/0|0/0|1/1|
+|IGLV|0/0|0/0|3/3|
+|IGIV|0/0|0/0|0/0|
+
+_Number of genes / number of alleles_
+
 ## Monodelphis domestica / Gray short-tailed opossum
 
 | Kind | V | J | C |
@@ -664,7 +675,7 @@ _Number of genes / number of alleles_
 |------|---|---|---|
 |IGHV|152/152|4/4|11/11|
 |IGKV|39/39|7/7|1/2|
-|IGLV|8/8|4/4|4/4|
+|IGLV|13/17|6/7|4/7|
 |IGIV|0/0|0/0|0/0|
 
 _Number of genes / number of alleles_
diff --git a/rustyms/src/imgt/germlines/mod.rs b/rustyms/src/imgt/germlines/mod.rs
index f2858874..a3a86c6e 100644
--- a/rustyms/src/imgt/germlines/mod.rs
+++ b/rustyms/src/imgt/germlines/mod.rs
@@ -37,6 +37,7 @@ Species::MacacaMulatta => Some(lock_MacacaMulatta()),
 Species::MacacaNemestrina => Some(lock_MacacaNemestrina()),
 Species::MacacaSilenus => Some(lock_MacacaSilenus()),
 Species::MacacaThibetana => Some(lock_MacacaThibetana()),
+Species::MesocricetusAuratus => Some(lock_MesocricetusAuratus()),
 Species::MonodelphisDomestica => Some(lock_MonodelphisDomestica()),
 Species::MusCookii => Some(lock_MusCookii()),
 Species::MusMinutoides => Some(lock_MusMinutoides()),
@@ -111,6 +112,7 @@ lock_MacacaMulatta(),
 lock_MacacaNemestrina(),
 lock_MacacaSilenus(),
 lock_MacacaThibetana(),
+lock_MesocricetusAuratus(),
 lock_MonodelphisDomestica(),
 lock_MusCookii(),
 lock_MusMinutoides(),
@@ -189,6 +191,7 @@ lock_MacacaMulatta(),
 lock_MacacaNemestrina(),
 lock_MacacaSilenus(),
 lock_MacacaThibetana(),
+lock_MesocricetusAuratus(),
 lock_MonodelphisDomestica(),
 lock_MusCookii(),
 lock_MusMinutoides(),
@@ -294,6 +297,8 @@ static LOCK_MacacaSilenus: OnceLock<Germlines> = OnceLock::new();
 fn lock_MacacaSilenus()->&'static Germlines{LOCK_MacacaSilenus.get_or_init(|| {bincode::deserialize(include_bytes!("Liontail macaque.bin")).unwrap()})}
 static LOCK_MacacaThibetana: OnceLock<Germlines> = OnceLock::new();
 fn lock_MacacaThibetana()->&'static Germlines{LOCK_MacacaThibetana.get_or_init(|| {bincode::deserialize(include_bytes!("Pere David's macaque.bin")).unwrap()})}
+static LOCK_MesocricetusAuratus: OnceLock<Germlines> = OnceLock::new();
+fn lock_MesocricetusAuratus()->&'static Germlines{LOCK_MesocricetusAuratus.get_or_init(|| {bincode::deserialize(include_bytes!("Golden hamster.bin")).unwrap()})}
 static LOCK_MonodelphisDomestica: OnceLock<Germlines> = OnceLock::new();
 fn lock_MonodelphisDomestica()->&'static Germlines{LOCK_MonodelphisDomestica.get_or_init(|| {bincode::deserialize(include_bytes!("Gray short-tailed opossum.bin")).unwrap()})}
 static LOCK_MusCookii: OnceLock<Germlines> = OnceLock::new();
diff --git a/rustyms/src/imgt/mod.rs b/rustyms/src/imgt/mod.rs
index 5bcefba1..962dde28 100644
--- a/rustyms/src/imgt/mod.rs
+++ b/rustyms/src/imgt/mod.rs
@@ -30,5 +30,5 @@ use germlines::par_germlines;
 use germlines::{all_germlines, germlines};
 
 pub use select::*;
-#[allow(unused_imports)]
+#[expect(unused_imports)]
 pub use shared::*;
diff --git a/rustyms/src/imgt/select.rs b/rustyms/src/imgt/select.rs
index 8d2b7a89..7c0d6614 100644
--- a/rustyms/src/imgt/select.rs
+++ b/rustyms/src/imgt/select.rs
@@ -2,8 +2,8 @@
 use rayon::prelude::*;
 use std::collections::HashSet;
 
-use crate::peptide::{AnnotatedPeptide, Annotation, Region, UnAmbiguous};
-use crate::LinearPeptide;
+use crate::peptidoform::{AnnotatedPeptide, Annotation, Region, UnAmbiguous};
+use crate::Peptidoform;
 
 pub use super::fancy::FancyDisplay;
 pub use super::shared::*;
@@ -171,7 +171,7 @@ pub struct Allele<'a> {
     /// The allele number, in IMGT this follows the name, eg `*01` is the allele in `IGHV3-23*01`
     pub number: usize,
     /// The actual sequence, the sequences present in the database are pure amino acids, no modifications are to be expected
-    pub sequence: &'a LinearPeptide<UnAmbiguous>,
+    pub sequence: &'a Peptidoform<UnAmbiguous>,
     /// The regions in the sequence, every region has an annotation and a length, all lengths together are the same length as the full sequence
     pub regions: &'a [(Region, usize)],
     /// Any additional annotations, every annotation has beside the kind it is also its location, as index in the sequence
@@ -192,7 +192,7 @@ impl<'a> Allele<'a> {
 
 impl<'a> AnnotatedPeptide for Allele<'a> {
     type Complexity = UnAmbiguous;
-    fn peptide(&self) -> &LinearPeptide<Self::Complexity> {
+    fn peptide(&self) -> &Peptidoform<Self::Complexity> {
         self.sequence
     }
     fn annotations(&self) -> &[(Annotation, usize)] {
@@ -258,7 +258,7 @@ impl Germlines {
 }
 
 #[cfg(test)]
-#[allow(clippy::missing_panics_doc)]
+#[expect(clippy::missing_panics_doc)]
 mod tests {
     use std::collections::HashSet;
 
diff --git a/rustyms/src/imgt/shared/regions.rs b/rustyms/src/imgt/shared/regions.rs
index c40bffd3..99d1008a 100644
--- a/rustyms/src/imgt/shared/regions.rs
+++ b/rustyms/src/imgt/shared/regions.rs
@@ -1,7 +1,7 @@
 #![allow(dead_code)]
 use crate::{
-    peptide::{Annotation, Region},
-    LinearPeptide, UnAmbiguous,
+    peptidoform::{Annotation, Region},
+    Peptidoform, UnAmbiguous,
 };
 use serde::{Deserialize, Serialize};
 use std::{fmt::Display, str::FromStr};
@@ -304,7 +304,7 @@ impl<'a> IntoParallelIterator for &'a Germline {
 #[derive(Clone, Serialize, Deserialize, Debug)]
 pub struct AnnotatedSequence {
     /// The sequence
-    pub sequence: LinearPeptide<UnAmbiguous>,
+    pub sequence: Peptidoform<UnAmbiguous>,
     /// The different regions in the sequence, defined by their name and length
     pub regions: Vec<(Region, usize)>,
     /// 0 based locations of single amino acid annotations, overlapping with the regions defined above
@@ -314,7 +314,7 @@ pub struct AnnotatedSequence {
 impl AnnotatedSequence {
     /// Create a new annotated sequence
     pub fn new(
-        sequence: LinearPeptide<UnAmbiguous>,
+        sequence: Peptidoform<UnAmbiguous>,
         regions: Vec<(Region, usize)>,
         mut conserved: Vec<(Annotation, usize)>,
     ) -> Self {
@@ -386,7 +386,7 @@ impl Gene {
     /// Get an IMGT name with allele, eg IGHV3-23*03
     /// # Errors
     /// If not recognised as a name, returns a description of the error.
-    #[allow(clippy::missing_panics_doc)] // Cannot panic
+    #[expect(clippy::missing_panics_doc)] // Cannot panic
     pub fn from_imgt_name_with_allele(s: &str) -> Result<(Self, usize), String> {
         let s = s.split(" or ").next().unwrap(); // Just ignore double names
         let (gene, tail) = Self::from_imgt_name_internal(s)?;
@@ -413,7 +413,7 @@ impl Gene {
     /// # Errors
     /// If not recognised as a name, returns a description of the error.
     fn from_imgt_name_internal(s: &str) -> Result<(Self, &str), String> {
-        #[allow(clippy::missing_panics_doc)] // Cannot panic
+        #[expect(clippy::missing_panics_doc)] // Cannot panic
         fn parse_name(s: &str) -> (Option<(Option<usize>, String)>, &str) {
             let num = s
                 .chars()
@@ -618,7 +618,7 @@ impl Display for GeneType {
     }
 }
 
-#[allow(clippy::missing_panics_doc)]
+#[expect(clippy::missing_panics_doc)]
 #[test]
 fn imgt_names() {
     assert_eq!(
diff --git a/rustyms/src/isobaric_sets.rs b/rustyms/src/isobaric_sets.rs
index c75eb456..64297d20 100644
--- a/rustyms/src/isobaric_sets.rs
+++ b/rustyms/src/isobaric_sets.rs
@@ -5,11 +5,10 @@ use itertools::Itertools;
 use crate::{
     checked_aminoacid::CheckedAminoAcid,
     modification::{Modification, SimpleModification, SimpleModificationInner},
-    peptide::SimpleLinear,
+    peptidoform::SimpleLinear,
     placement_rule::{PlacementRule, Position},
     system::{fraction, Mass, Ratio},
-    AminoAcid, Chemical, LinearPeptide, SemiAmbiguous, SequenceElement, SequencePosition,
-    Tolerance,
+    AminoAcid, Chemical, Peptidoform, SemiAmbiguous, SequenceElement, SequencePosition, Tolerance,
 };
 
 /// A list of building blocks for a sequence defined by its sequence elements and its mass.
@@ -120,7 +119,7 @@ pub fn building_blocks(
                 )
             })
             .flat_map(|(a, m)| {
-                #[allow(clippy::redundant_clone)] // not redundant
+                #[expect(clippy::redundant_clone)] // not redundant
                 let mc = m.clone();
                 a.formulas_all(
                     &[],
@@ -231,7 +230,7 @@ pub fn find_isobaric_sets(
     amino_acids: &[AminoAcid],
     fixed: &[(SimpleModification, Option<PlacementRule>)],
     variable: &[(SimpleModification, Option<PlacementRule>)],
-    base: Option<&LinearPeptide<SimpleLinear>>,
+    base: Option<&Peptidoform<SimpleLinear>>,
 ) -> IsobaricSetIterator {
     let bounds = tolerance.bounds(mass);
     let base_mass = base
@@ -258,7 +257,7 @@ pub struct IsobaricSetIterator {
     sizes: (Mass, Mass),
     bounds: (Mass, Mass),
     state: (Option<usize>, Option<usize>, Vec<usize>),
-    base: Option<LinearPeptide<SimpleLinear>>,
+    base: Option<Peptidoform<SimpleLinear>>,
 }
 
 impl IsobaricSetIterator {
@@ -270,7 +269,7 @@ impl IsobaricSetIterator {
         c_term: Vec<(SequenceElement<SemiAmbiguous>, SimpleModification, Mass)>,
         center: Vec<(SequenceElement<SemiAmbiguous>, Mass)>,
         bounds: (Mass, Mass),
-        base: Option<&LinearPeptide<SimpleLinear>>,
+        base: Option<&Peptidoform<SimpleLinear>>,
     ) -> Self {
         let sizes = (center.first().unwrap().1, center.last().unwrap().1);
         let mut iter = Self {
@@ -313,28 +312,25 @@ impl IsobaricSetIterator {
 
     /// # Panics
     /// If the base sequence is empty.
-    fn peptide(&self) -> LinearPeptide<SimpleLinear> {
+    fn peptide(&self) -> Peptidoform<SimpleLinear> {
         let mut sequence = Vec::with_capacity(
-            self.base
-                .as_ref()
-                .map(LinearPeptide::len)
-                .unwrap_or_default()
+            self.base.as_ref().map(Peptidoform::len).unwrap_or_default()
                 + self.state.2.len()
                 + usize::from(self.state.0.is_some())
                 + usize::from(self.state.1.is_some()),
         );
-        if let Some((b, _)) = self
+        if self
             .base
             .as_ref()
-            .and_then(|b| b.get_n_term().map(|n| (b, n.clone())))
+            .is_some_and(|b| !b.get_n_term().is_empty())
         {
-            sequence.push(b.sequence()[0].clone());
+            sequence.push(self.base.as_ref().unwrap().sequence()[0].clone());
         } else if let Some(n) = self.state.0.map(|i| self.n_term[i].clone()) {
             sequence.push(n.0.into());
         }
         if let Some(base) = &self.base {
-            let n = usize::from(base.get_n_term().is_some());
-            let c = usize::from(base.get_c_term().is_some());
+            let n = usize::from(base.get_n_term().is_empty());
+            let c = usize::from(base.get_c_term().is_empty());
             sequence.extend(base.sequence()[n..base.len() - n - c].iter().cloned());
         }
         sequence.extend(
@@ -344,36 +340,40 @@ impl IsobaricSetIterator {
                 .copied()
                 .map(|i| self.center[i].0.clone().into()),
         );
-        if let Some((b, _)) = self
+        if self
             .base
             .as_ref()
-            .and_then(|b| b.get_c_term().map(|c| (b, c.clone())))
+            .is_some_and(|b| !b.get_c_term().is_empty())
         {
-            sequence.push(b.sequence().last().unwrap().clone());
+            sequence.push(
+                self.base
+                    .as_ref()
+                    .unwrap()
+                    .sequence()
+                    .last()
+                    .unwrap()
+                    .clone(),
+            );
         } else if let Some(c) = self.state.1.map(|i| self.c_term[i].clone()) {
             sequence.push(c.0.into());
         }
-        LinearPeptide::new(sequence)
-            .n_term(
-                self.base
-                    .as_ref()
-                    .and_then(|b| b.get_n_term().cloned())
-                    .or_else(|| {
-                        self.state
-                            .0
-                            .map(|i| Modification::Simple(self.n_term[i].1.clone()))
-                    }),
-            )
-            .c_term(
-                self.base
-                    .as_ref()
-                    .and_then(|b| b.get_c_term().cloned())
-                    .or_else(|| {
-                        self.state
-                            .1
-                            .map(|i| Modification::Simple(self.c_term[i].1.clone()))
-                    }),
-            )
+        Peptidoform::new(sequence)
+            .n_term(self.base.as_ref().map_or_else(
+                || {
+                    self.state.0.map_or(Vec::new(), |i| {
+                        vec![Modification::Simple(self.n_term[i].1.clone())]
+                    })
+                },
+                |b| b.get_n_term().to_vec(),
+            ))
+            .c_term(self.base.as_ref().map_or_else(
+                || {
+                    self.state.0.map_or(Vec::new(), |i| {
+                        vec![Modification::Simple(self.c_term[i].1.clone())]
+                    })
+                },
+                |b| b.get_c_term().to_vec(),
+            ))
     }
 
     /// Reset the state for the center selection
@@ -386,7 +386,7 @@ impl IsobaricSetIterator {
 }
 
 impl Iterator for IsobaricSetIterator {
-    type Item = LinearPeptide<SimpleLinear>;
+    type Item = Peptidoform<SimpleLinear>;
     fn next(&mut self) -> Option<Self::Item> {
         loop {
             // N terminal loop
@@ -462,7 +462,10 @@ impl Iterator for IsobaricSetIterator {
                     }
                     self.state.1 = Some(c + 1);
                 } else if self.c_term.is_empty()
-                    || self.base.as_ref().is_some_and(|b| b.get_c_term().is_some())
+                    || self
+                        .base
+                        .as_ref()
+                        .is_some_and(|b| !b.get_c_term().is_empty())
                 {
                     // If the base piece has a defined C term mod do not try possible C term mods in the isobaric generation
                     break;
@@ -478,7 +481,10 @@ impl Iterator for IsobaricSetIterator {
                 }
                 self.state.0 = Some(n + 1);
             } else if self.n_term.is_empty()
-                || self.base.as_ref().is_some_and(|b| b.get_n_term().is_some())
+                || self
+                    .base
+                    .as_ref()
+                    .is_some_and(|b| !b.get_n_term().is_empty())
             {
                 // If the base piece has a defined N term mod do not try possible N term mods in the isobaric generation
                 break;
@@ -492,17 +498,17 @@ impl Iterator for IsobaricSetIterator {
 }
 
 #[cfg(test)]
-#[allow(clippy::missing_panics_doc)]
+#[expect(clippy::missing_panics_doc)]
 mod tests {
 
     use super::*;
     #[test]
     fn simple_isobaric_sets() {
-        let pep = LinearPeptide::pro_forma("AG", None)
+        let pep = Peptidoform::pro_forma("AG", None)
             .unwrap()
             .into_unambiguous()
             .unwrap();
-        let sets: Vec<LinearPeptide<SimpleLinear>> = find_isobaric_sets(
+        let sets: Vec<Peptidoform<SimpleLinear>> = find_isobaric_sets(
             pep.bare_formula().monoisotopic_mass(),
             Tolerance::new_ppm(10.0),
             AminoAcid::UNIQUE_MASS_AMINO_ACIDS,
@@ -514,11 +520,11 @@ mod tests {
         assert_eq!(
             &sets,
             &[
-                LinearPeptide::pro_forma("GA", None)
+                Peptidoform::pro_forma("GA", None)
                     .unwrap()
                     .into_simple_linear()
                     .unwrap(),
-                LinearPeptide::pro_forma("Q", None)
+                Peptidoform::pro_forma("Q", None)
                     .unwrap()
                     .into_simple_linear()
                     .unwrap(),
diff --git a/rustyms/src/isotopes.rs b/rustyms/src/isotopes.rs
index b5a99a9b..a1094da1 100644
--- a/rustyms/src/isotopes.rs
+++ b/rustyms/src/isotopes.rs
@@ -13,7 +13,7 @@ impl MolecularFormula {
     /// This approximation slightly overestimates the tail end of the distribution. Especially
     /// for species with multiple higher mass isotopes as it does not take the number of already
     /// chosen atom for lower weighed isotopes into account.
-    #[allow(clippy::missing_panics_doc)]
+    #[expect(clippy::missing_panics_doc)]
     pub fn isotopic_distribution(&self, threshold: f64) -> Array1<f64> {
         let mut result = arr1(&[1.0]);
         for (element, isotope, amount) in self.elements() {
diff --git a/rustyms/src/lib.rs b/rustyms/src/lib.rs
index 7c50b66a..96d410f9 100644
--- a/rustyms/src/lib.rs
+++ b/rustyms/src/lib.rs
@@ -39,6 +39,7 @@ mod aminoacids;
 mod checked_aminoacid;
 mod element;
 pub mod error;
+mod formula_search;
 pub mod fragment;
 pub mod glycan;
 mod isobaric_sets;
@@ -54,7 +55,7 @@ mod multi;
 mod mzpaf;
 mod neutral_loss;
 pub mod ontologies;
-pub mod peptide;
+pub mod peptidoform;
 pub mod placement_rule;
 mod protease;
 #[cfg(feature = "rand")]
@@ -70,6 +71,7 @@ mod tolerance;
 
 pub use crate::element::*;
 pub use crate::formula::*;
+pub use crate::formula_search::find_formulas;
 pub use crate::isobaric_sets::{building_blocks, find_isobaric_sets};
 pub use crate::mass_mode::MassMode;
 pub use crate::model::Model;
@@ -77,7 +79,7 @@ pub use crate::modification::{CrossLinkName, Modification};
 pub use crate::molecular_charge::MolecularCharge;
 pub use crate::multi::*;
 pub use crate::neutral_loss::*;
-pub use crate::peptide::*;
+pub use crate::peptidoform::*;
 pub use crate::protease::*;
 pub use crate::sequence_element::SequenceElement;
 pub use crate::sequence_position::*;
@@ -86,19 +88,19 @@ pub use crate::tolerance::*;
 pub use aminoacids::AminoAcid;
 pub use checked_aminoacid::CheckedAminoAcid;
 pub use fragment::Fragment;
-pub use peptide::{CompoundPeptidoform, LinearPeptide, Peptidoform};
+pub use peptidoform::{CompoundPeptidoformIon, Peptidoform, PeptidoformIon};
 
 #[macro_use]
 extern crate uom;
 
 #[cfg(test)]
-#[allow(clippy::missing_panics_doc)]
+#[expect(clippy::missing_panics_doc)]
 mod test {
     use super::*;
 
     #[test]
     fn simple_fragments() {
-        let peptide = LinearPeptide::pro_forma("WFWF", None)
+        let peptide = Peptidoform::pro_forma("WFWF", None)
             .unwrap()
             .into_linear()
             .unwrap();
@@ -114,7 +116,7 @@ mod test {
     fn simple_matching() {
         let model = Model::all();
         let spectrum = rawfile::mgf::open("data/example.mgf").unwrap();
-        let peptide = CompoundPeptidoform::pro_forma("WFWF", None).unwrap();
+        let peptide = CompoundPeptidoformIon::pro_forma("WFWF", None).unwrap();
         let fragments = peptide
             .generate_theoretical_fragments(system::usize::Charge::new::<system::e>(1), &model);
         let annotated = spectrum[0].annotate(peptide, &fragments, &model, MassMode::Monoisotopic);
diff --git a/rustyms/src/model.rs b/rustyms/src/model.rs
index 0fd241ce..3838f741 100644
--- a/rustyms/src/model.rs
+++ b/rustyms/src/model.rs
@@ -77,7 +77,6 @@ impl ChargePoint {
 /// A model for the fragmentation, allowing control over what theoretical fragments to generate.
 #[non_exhaustive]
 #[derive(Clone, PartialEq, Debug, Serialize, Deserialize)]
-#[allow(clippy::struct_excessive_bools)]
 pub struct Model {
     /// a series ions
     pub a: PrimaryIonSeries,
@@ -238,7 +237,6 @@ impl GlycanModel {
 }
 
 /// A struct to handle all possible fragments that could be generated on a single location
-#[allow(clippy::struct_excessive_bools)]
 #[derive(Clone, PartialEq, Eq, PartialOrd, Ord, Debug, Hash)]
 #[non_exhaustive]
 pub struct PossibleIons<'a> {
@@ -266,7 +264,7 @@ pub struct PossibleIons<'a> {
     pub immonium: (bool, ChargeRange),
 }
 
-impl<'a> PossibleIons<'a> {
+impl PossibleIons<'_> {
     /// Give an upper bound for the number of theoretical fragment for these possible ions
     pub fn size_upper_bound(&self) -> usize {
         usize::from(self.a.0) * (self.a.1.len() + 1)
@@ -786,7 +784,7 @@ impl Location {
 }
 
 #[test]
-#[allow(clippy::missing_panics_doc, clippy::similar_names)]
+#[expect(clippy::missing_panics_doc, clippy::similar_names)]
 fn location_all() {
     let all = Model::all();
     let ions_n0 = all.ions(PeptidePosition::n(crate::SequencePosition::default(), 2));
diff --git a/rustyms/src/modification.rs b/rustyms/src/modification.rs
index 64f3b2fc..d0024055 100644
--- a/rustyms/src/modification.rs
+++ b/rustyms/src/modification.rs
@@ -14,11 +14,11 @@ use std::{
 use crate::{
     glycan::{GlycanStructure, MonoSaccharide},
     molecular_charge::CachedCharge,
-    peptide::Linked,
+    peptidoform::Linked,
     placement_rule::{PlacementRule, Position},
     system::OrderedMass,
-    AmbiguousLabel, AminoAcid, Chemical, DiagnosticIon, Fragment, LinearPeptide, Model,
-    MolecularFormula, Multi, NeutralLoss, SequenceElement, SequencePosition,
+    AmbiguousLabel, AminoAcid, Chemical, DiagnosticIon, Fragment, Model, MolecularFormula, Multi,
+    NeutralLoss, Peptidoform, SequenceElement, SequencePosition,
 };
 
 include!("shared/modification.rs");
@@ -99,7 +99,11 @@ impl std::iter::Sum for RulePossible {
 
 impl Chemical for SimpleModificationInner {
     /// Get the molecular formula for this modification.
-    fn formula_inner(&self, position: SequencePosition, peptide_index: usize) -> MolecularFormula {
+    fn formula_inner(
+        &self,
+        position: SequencePosition,
+        peptidoform_index: usize,
+    ) -> MolecularFormula {
         match self {
             Self::Mass(m)
             | Self::Gno {
@@ -113,13 +117,13 @@ impl Chemical for SimpleModificationInner {
             | Self::Glycan(monosaccharides) => monosaccharides
                 .iter()
                 .fold(MolecularFormula::default(), |acc, i| {
-                    acc + i.0.formula_inner(position, peptide_index) * i.1 as i32
+                    acc + i.0.formula_inner(position, peptidoform_index) * i.1 as i32
                 }),
             Self::GlycanStructure(glycan)
             | Self::Gno {
                 composition: GnoComposition::Topology(glycan),
                 ..
-            } => glycan.formula_inner(position, peptide_index),
+            } => glycan.formula_inner(position, peptidoform_index),
             Self::Formula(formula)
             | Self::Database { formula, .. }
             | Self::Linker { formula, .. } => formula.clone(),
@@ -129,7 +133,6 @@ impl Chemical for SimpleModificationInner {
 
 impl SimpleModificationInner {
     /// Get a url for more information on this modification. Only defined for modifications from ontologies.
-    #[allow(clippy::missing_panics_doc)]
     pub fn ontology_url(&self) -> Option<String> {
         match self {
             Self::Mass(_) | Self::Formula(_) | Self::Glycan(_) | Self::GlycanStructure(_) => None,
@@ -141,7 +144,7 @@ impl SimpleModificationInner {
     pub(crate) fn formula_inner(
         &self,
         sequence_index: SequencePosition,
-        peptide_index: usize,
+        peptidoform_index: usize,
     ) -> MolecularFormula {
         match self {
             Self::Mass(m)
@@ -156,13 +159,13 @@ impl SimpleModificationInner {
             | Self::Glycan(monosaccharides) => monosaccharides
                 .iter()
                 .fold(MolecularFormula::default(), |acc, i| {
-                    acc + i.0.formula_inner(sequence_index, peptide_index) * i.1 as i32
+                    acc + i.0.formula_inner(sequence_index, peptidoform_index) * i.1 as i32
                 }),
             Self::GlycanStructure(glycan)
             | Self::Gno {
                 composition: GnoComposition::Topology(glycan),
                 ..
-            } => glycan.formula_inner(sequence_index, peptide_index),
+            } => glycan.formula_inner(sequence_index, peptidoform_index),
             Self::Formula(formula)
             | Self::Database { formula, .. }
             | Self::Linker { formula, .. } => formula.clone(),
@@ -176,6 +179,9 @@ impl SimpleModificationInner {
         position: SequencePosition,
     ) -> RulePossible {
         match self {
+            Self::Database { specificities, .. } if specificities.is_empty() => {
+                RulePossible::Symmetric(BTreeSet::default())
+            }
             Self::Database { specificities, .. } => {
                 // If any of the rules match the current situation then it can be placed
                 let matching: BTreeSet<usize> = specificities
@@ -191,6 +197,9 @@ impl SimpleModificationInner {
                     RulePossible::Symmetric(matching)
                 }
             }
+            Self::Linker { specificities, .. } if specificities.is_empty() => {
+                RulePossible::Symmetric(BTreeSet::default())
+            }
             Self::Linker { specificities, .. } => specificities
                 .iter()
                 .enumerate()
@@ -484,12 +493,12 @@ impl Modification {
     /// Get the formula for the whole addition (or subtraction) for this modification
     pub(crate) fn formula_inner(
         &self,
-        all_peptides: &[LinearPeptide<Linked>],
+        all_peptides: &[Peptidoform<Linked>],
         visited_peptides: &[usize],
         applied_cross_links: &mut Vec<CrossLinkName>,
         allow_ms_cleavable: bool,
         sequence_index: SequencePosition,
-        peptide_index: usize,
+        peptidoform_index: usize,
     ) -> (Multi<MolecularFormula>, HashSet<CrossLinkName>) {
         match self {
             Self::Simple(modification) | Self::Ambiguous { modification, .. } => {
@@ -500,7 +509,7 @@ impl Modification {
                         HashSet::new(),
                     ),
                     s => (
-                        s.formula_inner(sequence_index, peptide_index).into(),
+                        s.formula_inner(sequence_index, peptidoform_index).into(),
                         HashSet::new(),
                     ),
                 }
@@ -518,14 +527,14 @@ impl Modification {
                     applied_cross_links.push(name.clone());
                     (
                         linker
-                            .formula_inner(sequence_index, peptide_index)
+                            .formula_inner(sequence_index, peptidoform_index)
                             .with_label(AmbiguousLabel::CrossLinkBound(name.clone()))
                             .into(),
                         HashSet::from([name.clone()]),
                     )
                 } else {
                     applied_cross_links.push(name.clone());
-                    let link = linker.formula_inner(sequence_index, peptide_index);
+                    let link = linker.formula_inner(sequence_index, peptidoform_index);
                     let (_, stubs, _) = side.allowed_rules(linker);
 
                     if allow_ms_cleavable && !stubs.is_empty() {
@@ -583,9 +592,7 @@ impl Modification {
             Self::Ambiguous { modification, .. } => modification.formula(),
         }
     }
-}
 
-impl Modification {
     /// Check if this is a simple modification
     pub const fn simple(&self) -> Option<&SimpleModification> {
         match self {
@@ -603,7 +610,6 @@ impl Modification {
     }
 
     /// Get a url for more information on this modification. Only defined for modifications from ontologies.
-    #[allow(clippy::missing_panics_doc)]
     pub fn ontology_url(&self) -> Option<String> {
         match self {
             Self::Simple(modification)
@@ -631,8 +637,8 @@ impl Modification {
     pub(crate) fn generate_theoretical_fragments(
         &self,
         model: &Model,
+        peptidoform_ion_index: usize,
         peptidoform_index: usize,
-        peptide_index: usize,
         charge_carriers: &mut CachedCharge,
         full_formula: &Multi<MolecularFormula>,
         attachment: Option<(AminoAcid, usize)>,
@@ -641,8 +647,8 @@ impl Modification {
             Self::Simple(modification) | Self::Ambiguous { modification, .. } => modification
                 .generate_theoretical_fragments(
                     model,
+                    peptidoform_ion_index,
                     peptidoform_index,
-                    peptide_index,
                     charge_carriers,
                     full_formula,
                     attachment,
@@ -657,8 +663,8 @@ impl SimpleModificationInner {
     pub(crate) fn generate_theoretical_fragments(
         &self,
         model: &Model,
+        peptidoform_ion_index: usize,
         peptidoform_index: usize,
-        peptide_index: usize,
         charge_carriers: &mut CachedCharge,
         full_formula: &Multi<MolecularFormula>,
         attachment: Option<(AminoAcid, usize)>,
@@ -673,8 +679,8 @@ impl SimpleModificationInner {
                 .determine_positions()
                 .generate_theoretical_fragments(
                     model,
+                    peptidoform_ion_index,
                     peptidoform_index,
-                    peptide_index,
                     charge_carriers,
                     full_formula,
                     attachment,
@@ -686,8 +692,8 @@ impl SimpleModificationInner {
             } => MonoSaccharide::theoretical_fragments(
                 composition,
                 model,
+                peptidoform_ion_index,
                 peptidoform_index,
-                peptide_index,
                 charge_carriers,
                 full_formula,
                 attachment,
@@ -698,13 +704,68 @@ impl SimpleModificationInner {
 }
 
 /// The structure to lookup ambiguous modifications, with a list of all modifications (the order is fixed) with for each modification their name and the actual modification itself (if already defined)
-pub type AmbiguousLookup = Vec<(String, Option<SimpleModification>)>;
+pub type AmbiguousLookup = Vec<AmbiguousLookupEntry>;
+
+/// An entry in the ambiguous lookup
+#[derive(Debug, Clone)]
+pub struct AmbiguousLookupEntry {
+    /// The name of the modification
+    pub name: String,
+    /// The group of the modification
+    pub group: Option<usize>,
+    /// The modification itself
+    pub modification: Option<SimpleModification>,
+    /// The allowed locations, the actual allowed locations is the intersection of this set with the ruleset from the modification
+    position: Option<Vec<PlacementRule>>,
+    /// The maximal number of this modification on one place
+    limit: Option<usize>,
+    /// Determines if this modification can colocalise with placed modifications eg if the modification of unknown position is allowed at the second M '[Oxidation]?MM[Dioxidation]M'
+    colocalise_placed_modifications: bool,
+    /// Determines if this modification can colocalise with other modifications of unknown position
+    colocalise_modifications_of_unknown_position: bool,
+}
+
+impl AmbiguousLookupEntry {
+    /// Create a new ambiguous lookup entry
+    pub const fn new(name: String, modification: Option<SimpleModification>) -> Self {
+        Self {
+            name,
+            group: None,
+            modification,
+            limit: None,
+            position: None,
+            colocalise_placed_modifications: true,
+            colocalise_modifications_of_unknown_position: true,
+        }
+    }
+
+    /// Copy settings into this lookup entry
+    pub fn copy_settings(&mut self, settings: &crate::MUPSettings) {
+        self.position.clone_from(&settings.position);
+        self.limit = settings.limit;
+        self.colocalise_placed_modifications = settings.colocalise_placed_modifications;
+        self.colocalise_modifications_of_unknown_position =
+            settings.colocalise_modifications_of_unknown_position;
+    }
+
+    /// Get the settings for this modification of unknown position
+    pub fn as_settings(&self) -> crate::MUPSettings {
+        crate::MUPSettings {
+            position: self.position.clone(),
+            limit: self.limit,
+            colocalise_placed_modifications: self.colocalise_placed_modifications,
+            colocalise_modifications_of_unknown_position: self
+                .colocalise_modifications_of_unknown_position,
+        }
+    }
+}
+
 /// The structure to lookup cross-links, with a list of all linkers (the order is fixed) with for each linker their name or None if it is a branch and the actual linker itself (if already defined)
 pub type CrossLinkLookup = Vec<(CrossLinkName, Option<SimpleModification>)>;
 
 impl Modification {
     /// Display a modification either normalised to the internal representation or as fully valid ProForma
-    /// (no glycan structure or custom modifications). 'display_ambiguous' shows or hides the modification
+    /// (no glycan structure or custom modifications). `display_ambiguous` shows or hides the modification
     /// definition of any ambiguous modifications (eg true results in '+1#1' false in '#1').
     /// # Errors
     /// When the given writer errors.
@@ -761,7 +822,7 @@ impl Display for CrossLinkName {
 include!("shared/ontology.rs");
 
 #[test]
-#[allow(clippy::missing_panics_doc)]
+#[expect(clippy::missing_panics_doc)]
 fn test_reading_custom_modifications_json() {
     use serde_json;
     let data = r#"[ [ 1, "uranium linker", { "Linker": { "specificities": [ { "Asymmetric": [ [ [ { "AminoAcid": [ [ "Selenocysteine" ], "AnyCTerm" ] }, { "AminoAcid": [ [ "GlutamicAcid" ], "Anywhere" ] } ], [ { "AminoAcid": [ [ "Selenocysteine" ], "AnyNTerm" ] } ] ], [ [ { "elements": [ [ "U", null, 1 ] ], "additional_mass": 0.0 }, { "elements": [ [ "U", null, 1 ] ], "additional_mass": 0.0 } ] ], [ { "elements": [ [ "Te", null, 1 ] ], "additional_mass": 0.0 }, { "elements": [ [ "Ne", null, 1 ] ], "additional_mass": 0.0 }, { "elements": [ [ "H", null, 2 ], [ "He", null, 3 ] ], "additional_mass": 0.0 }, { "elements": [ [ "H", null, 1 ], [ "He", null, 2 ] ], "additional_mass": 0.0 }, { "elements": [ [ "I", null, 1 ], [ "Er", null, 1 ] ], "additional_mass": 0.0 }, { "elements": [ [ "H", null, 12 ], [ "C", null, 12 ], [ "O", null, 1 ] ], "additional_mass": 0.0 } ] ] } ], "formula": { "elements": [ [ "U", null, 2 ] ], "additional_mass": 0.0 }, "id": { "ontology": "Custom", "name": "Uranium linker", "id": 1, "description": "Have some uranium, its delicious!", "synonyms": [], "cross_ids": [ [ "Pubmed", "21714143" ] ] }, "length": 23.9 } } ], [ 2, "helium", { "Database": { "specificities": [ [ [ { "AminoAcid": [ [ "Alanine" ], "Anywhere" ] } ], [], [] ], [ [ { "AminoAcid": [ [ "Methionine" ], "Anywhere" ] } ], [ { "Loss": { "elements": [], "additional_mass": 12.0 } } ], [] ] ], "formula": { "elements": [ [ "He", null, 2 ] ], "additional_mass": 0.0 }, "id": { "ontology": "Custom", "name": "Helium", "id": 2, "description": "heeeelium", "synonyms": [ "heeeelium", "funny gas" ], "cross_ids": [ [ "Pubmed", "42" ], [ "Unimod", "12" ], [ "Resid", "A12" ] ] } } } ], [ 3, "db18", { "Database": { "specificities": [ [ [ { "AminoAcid": [ [ "Cysteine" ], "Anywhere" ] } ], [ { "Gain": { "elements": [], "additional_mass": 372.25 } }, { "Gain": { "elements": [], "additional_mass": 373.258 } }, { "Gain": { "elements": [], "additional_mass": 371.242 } }, { "Gain": { "elements": [], "additional_mass": 240.171 } }, { "Gain": { "elements": [], "additional_mass": 239.163 } }, { "Gain": { "elements": [], "additional_mass": 241.179 } }, { "Gain": { "elements": [], "additional_mass": 197.129 } }, { "Gain": { "elements": [], "additional_mass": 198.137 } }, { "Gain": { "elements": [], "additional_mass": 196.121 } }, { "Gain": { "elements": [], "additional_mass": 619.418 } }, { "Gain": { "elements": [], "additional_mass": 621.4343 } }, { "Gain": { "elements": [], "additional_mass": 649.465 } }, { "Gain": { "elements": [], "additional_mass": 677.497 } }, { "Gain": { "elements": [], "additional_mass": 618.41 } }, { "Gain": { "elements": [], "additional_mass": 620.426 } }, { "Gain": { "elements": [], "additional_mass": 648.457 } }, { "Gain": { "elements": [], "additional_mass": 676.489 } }, { "Gain": { "elements": [], "additional_mass": 620.426 } }, { "Gain": { "elements": [], "additional_mass": 622.442 } }, { "Gain": { "elements": [], "additional_mass": 650.473 } }, { "Gain": { "elements": [], "additional_mass": 678.504 } }, { "Gain": { "elements": [], "additional_mass": 28.006 } } ], [ { "elements": [], "additional_mass": 372.25 }, { "elements": [], "additional_mass": 240.171 }, { "elements": [], "additional_mass": 197.129 }, { "elements": [], "additional_mass": 619.418 }, { "elements": [], "additional_mass": 621.434 }, { "elements": [], "additional_mass": 649.465 }, { "elements": [], "additional_mass": 677.497 } ] ] ], "formula": { "elements": [], "additional_mass": 676.489 }, "id": { "ontology": "Custom", "name": "DB18", "id": 3, "description": "", "synonyms": [], "cross_ids": [] } } } ], [ 4, "disulfide", { "Linker": { "specificities": [ { "Symmetric": [ [ { "AminoAcid": [ [ "Cysteine" ], "Anywhere" ] } ], [ [ { "elements": [], "additional_mass": 0.0 }, { "elements": [], "additional_mass": 0.0 } ], [ { "elements": [ [ "H", null, -1 ] ], "additional_mass": 0.0 }, { "elements": [], "additional_mass": 0.0 } ], [ { "elements": [ [ "H", null, -1 ] ], "additional_mass": 0.0 }, { "elements": [ [ "H", null, -1 ] ], "additional_mass": 0.0 } ] ], [] ] } ], "formula": { "elements": [ [ "H", null, -2 ] ], "additional_mass": 0.0 }, "id": { "ontology": "Custom", "name": "Disulfide", "id": 4, "description": "A disulfide with all potential neutral losses", "synonyms": [], "cross_ids": [] }, "length": 0.0 } } ], [ 5, "dsso", { "Linker": { "specificities": [ { "Symmetric": [ [ { "AminoAcid": [ [ "Lysine" ], "Anywhere" ] } ], [ [ { "elements": [ [ "H", null, 1 ], [ "C", null, 3 ], [ "N", null, -1 ], [ "O", null, 3 ], [ "S", null, 1 ] ], "additional_mass": 0.0 }, { "elements": [ [ "H", null, 1 ], [ "C", null, 3 ], [ "N", null, -1 ], [ "O", null, 2 ] ], "additional_mass": 0.0 } ] ], [] ] } ], "formula": { "elements": [ [ "H", null, 2 ], [ "C", null, 6 ], [ "N", null, -2 ], [ "O", null, 5 ], [ "S", null, 1 ] ], "additional_mass": 0.0 }, "id": { "ontology": "Custom", "name": "DSSO", "id": 5, "description": "", "synonyms": [], "cross_ids": [] }, "length": 0.0 } } ]]"#;
diff --git a/rustyms/src/molecular_charge.rs b/rustyms/src/molecular_charge.rs
index ea10a2df..1d498582 100644
--- a/rustyms/src/molecular_charge.rs
+++ b/rustyms/src/molecular_charge.rs
@@ -67,7 +67,7 @@ pub struct MolecularCharge {
 
 impl MolecularCharge {
     /// Create a default charge state with only protons
-    #[allow(clippy::missing_panics_doc)] // Cannot panic
+    #[expect(clippy::missing_panics_doc)] // Cannot panic
     pub fn proton(charge: isize) -> Self {
         Self {
             charge_carriers: vec![(
@@ -181,7 +181,7 @@ impl Chemical for MolecularCharge {
     fn formula_inner(
         &self,
         _sequence_index: SequencePosition,
-        _peptide_index: usize,
+        _peptidoform_index: usize,
     ) -> MolecularFormula {
         self.charge_carriers
             .iter()
@@ -227,7 +227,7 @@ impl std::fmt::Display for MolecularCharge {
 }
 
 #[cfg(test)]
-#[allow(clippy::missing_panics_doc)]
+#[expect(clippy::missing_panics_doc)]
 mod tests {
     use crate::Chemical;
 
diff --git a/rustyms/src/neutral_loss.rs b/rustyms/src/neutral_loss.rs
index 24f037ba..b5d2ee2d 100644
--- a/rustyms/src/neutral_loss.rs
+++ b/rustyms/src/neutral_loss.rs
@@ -11,6 +11,9 @@ use crate::{
 include!("shared/neutral_loss.rs");
 
 impl NeutralLoss {
+    // TODO: extend with full list from annotator, plus figure out a way to make them const
+    //const WATER_LOSS: Self = Self::Loss(molecular_formula!(H 2 O 1));
+
     /// Check if this neutral loss if empty (has an empty molecular formula)
     pub fn is_empty(&self) -> bool {
         match self {
diff --git a/rustyms/src/peptide/annotated.rs b/rustyms/src/peptidoform/annotated.rs
similarity index 97%
rename from rustyms/src/peptide/annotated.rs
rename to rustyms/src/peptidoform/annotated.rs
index c45ecbe4..a861fd7d 100644
--- a/rustyms/src/peptide/annotated.rs
+++ b/rustyms/src/peptidoform/annotated.rs
@@ -1,11 +1,11 @@
-use crate::LinearPeptide;
+use crate::Peptidoform;
 
 /// An annotated peptide
 pub trait AnnotatedPeptide {
     /// The complexity of the peptide
     type Complexity;
     /// Get the peptide
-    fn peptide(&self) -> &LinearPeptide<Self::Complexity>;
+    fn peptide(&self) -> &Peptidoform<Self::Complexity>;
     /// Get the regions, as a list of the regions in order with the length of each region, these are
     /// required to be as long as the full peptide.
     fn regions(&self) -> &[(Region, usize)];
@@ -44,7 +44,7 @@ use itertools::Itertools;
 use serde::{Deserialize, Serialize};
 
 /// A region on an antibody
-#[allow(missing_docs)]
+#[expect(missing_docs)]
 #[derive(Clone, PartialEq, Eq, Hash, Serialize, Deserialize, Debug)]
 pub enum Region {
     Framework(usize),
diff --git a/rustyms/src/peptide/complexity.rs b/rustyms/src/peptidoform/complexity.rs
similarity index 100%
rename from rustyms/src/peptide/complexity.rs
rename to rustyms/src/peptidoform/complexity.rs
diff --git a/rustyms/src/peptide/compound_peptidoform.rs b/rustyms/src/peptidoform/compound_peptidoform_ion.rs
similarity index 63%
rename from rustyms/src/peptide/compound_peptidoform.rs
rename to rustyms/src/peptidoform/compound_peptidoform_ion.rs
index c28b2c5f..87bd364c 100644
--- a/rustyms/src/peptide/compound_peptidoform.rs
+++ b/rustyms/src/peptidoform/compound_peptidoform_ion.rs
@@ -4,26 +4,26 @@ use itertools::Itertools;
 use serde::{Deserialize, Serialize};
 
 use crate::{
-    peptide::Linked, system::usize::Charge, Fragment, LinearPeptide, Model, MolecularFormula,
-    Multi, Peptidoform,
+    peptidoform::Linked, system::usize::Charge, Fragment, Model, MolecularFormula, Multi,
+    Peptidoform, PeptidoformIon,
 };
 
 /// A single full ProForma entry. This entry can contain multiple sets of cross-linked peptides.
-/// A single set of cross-linked peptides is a [`Peptidoform`]. A ProForma entry with two chimeric
-/// peptides will be saved as one [`CompoundPeptidoform`] with two [`Peptidoform`]s that each
-/// contain one of the [`LinearPeptide`]s.
+/// A single set of cross-linked peptides is a [`PeptidoformIon`]. A ProForma entry with two chimeric
+/// peptides will be saved as one [`CompoundPeptidoformIon`] with two [`PeptidoformIon`]s that each
+/// contain one of the [`Peptidoform`]s.
 #[derive(Clone, PartialEq, Eq, PartialOrd, Ord, Debug, Serialize, Deserialize, Hash)]
-pub struct CompoundPeptidoform(pub(super) Vec<Peptidoform>);
+pub struct CompoundPeptidoformIon(pub(super) Vec<PeptidoformIon>);
 
-impl CompoundPeptidoform {
+impl CompoundPeptidoformIon {
     /// Create a new [`CompoundPeptidoform`] from many [`Peptidoform`]s. This returns None if the
     /// global isotope modifications of all peptidoforms are not identical.
-    pub fn new(iter: impl IntoIterator<Item = Peptidoform>) -> Option<Self> {
+    pub fn new(iter: impl IntoIterator<Item = PeptidoformIon>) -> Option<Self> {
         let result = Self(iter.into_iter().collect());
         let global_equal = result
-            .peptidoforms()
+            .peptidoform_ions()
             .iter()
-            .flat_map(Peptidoform::peptides)
+            .flat_map(PeptidoformIon::peptidoforms)
             .tuple_windows()
             .all(|(a, b)| a.get_global() == b.get_global());
         global_equal.then_some(result)
@@ -36,7 +36,7 @@ impl CompoundPeptidoform {
 
     /// Assume there is exactly one peptidoform in this compound peptidoform.
     #[doc(alias = "assume_linear")]
-    pub fn singular(mut self) -> Option<Peptidoform> {
+    pub fn singular(mut self) -> Option<PeptidoformIon> {
         if self.0.len() == 1 {
             self.0.pop()
         } else {
@@ -45,18 +45,18 @@ impl CompoundPeptidoform {
     }
 
     /// Assume there is exactly one peptide in this compound peptidoform.
-    pub fn singular_peptide(self) -> Option<LinearPeptide<Linked>> {
-        self.singular().and_then(Peptidoform::singular)
+    pub fn singular_peptide(self) -> Option<Peptidoform<Linked>> {
+        self.singular().and_then(PeptidoformIon::singular)
     }
 
-    /// Get all peptidoforms making up this compound peptidoform.
-    pub fn peptidoforms(&self) -> &[Peptidoform] {
+    /// Get all peptidoform ions making up this compound peptidoform.
+    pub fn peptidoform_ions(&self) -> &[PeptidoformIon] {
         &self.0
     }
 
-    /// Get all peptides making up this compound peptidoform.
-    pub fn peptides(&self) -> impl Iterator<Item = &LinearPeptide<Linked>> {
-        self.0.iter().flat_map(Peptidoform::peptides)
+    /// Get all peptidoforms making up this compound peptidoform.
+    pub fn peptidoforms(&self) -> impl Iterator<Item = &Peptidoform<Linked>> {
+        self.0.iter().flat_map(PeptidoformIon::peptidoforms)
     }
 
     /// Generate the theoretical fragments for this compound peptidoform.
@@ -66,7 +66,7 @@ impl CompoundPeptidoform {
         model: &Model,
     ) -> Vec<Fragment> {
         let mut base = Vec::new();
-        for (index, peptidoform) in self.peptidoforms().iter().enumerate() {
+        for (index, peptidoform) in self.peptidoform_ions().iter().enumerate() {
             base.extend(peptidoform.generate_theoretical_fragments_inner(max_charge, model, index));
         }
         base
@@ -82,9 +82,9 @@ impl CompoundPeptidoform {
         // The global isotope modifications are guaranteed to be identical, so take the first
         let empty = Vec::new();
         let global = self
-            .peptidoforms()
+            .peptidoform_ions()
             .iter()
-            .flat_map(Peptidoform::peptides)
+            .flat_map(PeptidoformIon::peptidoforms)
             .next()
             .map_or(empty.as_slice(), |p| p.get_global());
         for (element, isotope) in global {
@@ -97,7 +97,7 @@ impl CompoundPeptidoform {
         }
 
         let mut first = true;
-        for p in self.peptidoforms() {
+        for p in self.peptidoform_ions() {
             if !first {
                 write!(f, "+")?;
             }
@@ -108,26 +108,26 @@ impl CompoundPeptidoform {
     }
 }
 
-impl Display for CompoundPeptidoform {
+impl Display for CompoundPeptidoformIon {
     fn fmt(&self, f: &mut std::fmt::Formatter<'_>) -> std::fmt::Result {
         self.display(f, true)
     }
 }
 
-impl<Complexity> From<LinearPeptide<Complexity>> for CompoundPeptidoform {
-    fn from(value: LinearPeptide<Complexity>) -> Self {
-        Self(vec![Peptidoform(vec![value.mark()])])
+impl<Complexity> From<Peptidoform<Complexity>> for CompoundPeptidoformIon {
+    fn from(value: Peptidoform<Complexity>) -> Self {
+        Self(vec![PeptidoformIon(vec![value.mark()])])
     }
 }
 
-impl From<Peptidoform> for CompoundPeptidoform {
-    fn from(value: Peptidoform) -> Self {
+impl From<PeptidoformIon> for CompoundPeptidoformIon {
+    fn from(value: PeptidoformIon) -> Self {
         Self(vec![value])
     }
 }
 
-impl<Complexity> From<Vec<LinearPeptide<Complexity>>> for CompoundPeptidoform {
-    fn from(value: Vec<LinearPeptide<Complexity>>) -> Self {
+impl<Complexity> From<Vec<Peptidoform<Complexity>>> for CompoundPeptidoformIon {
+    fn from(value: Vec<Peptidoform<Complexity>>) -> Self {
         Self(value.into_iter().map(Into::into).collect())
     }
 }
diff --git a/rustyms/src/peptide/find_modifications.rs b/rustyms/src/peptidoform/find_modifications.rs
similarity index 90%
rename from rustyms/src/peptide/find_modifications.rs
rename to rustyms/src/peptidoform/find_modifications.rs
index 8b6faf96..991172cc 100644
--- a/rustyms/src/peptide/find_modifications.rs
+++ b/rustyms/src/peptidoform/find_modifications.rs
@@ -1,5 +1,7 @@
 use std::collections::HashMap;
 
+use itertools::Itertools;
+
 use crate::{
     glycan::MonoSaccharide,
     modification::{GnoComposition, Ontology, SimpleModification, SimpleModificationInner},
@@ -9,7 +11,7 @@ use crate::{
     AminoAcid, Chemical, MassMode, Modification, MolecularFormula, Tolerance, WithinTolerance,
 };
 
-use super::LinearPeptide;
+use super::Peptidoform;
 
 /// Search for modifications that fit the mass tolerance and optional position requirements. If the
 /// `positions` is `None` it will not filter for possible positions. Otherwise only modifications
@@ -232,11 +234,11 @@ impl PeptideModificationSearch {
     }
 
     /// Search for modifications that can be replaced by named modifications in this peptide.
-    #[allow(clippy::similar_names)]
+    #[expect(clippy::similar_names)]
     pub fn search<Complexity>(
         &mut self,
-        mut peptide: LinearPeptide<Complexity>,
-    ) -> LinearPeptide<Complexity> {
+        mut peptide: Peptidoform<Complexity>,
+    ) -> Peptidoform<Complexity> {
         fn find_replacement_all_positions(
             settings: &mut PeptideModificationSearch,
             n_term: bool,
@@ -299,22 +301,32 @@ impl PeptideModificationSearch {
         }
 
         // Start with N and C terminal mods
-        let mut n_term = peptide.get_n_term().cloned().and_then(|m| {
-            find_replacement_modification(
-                self,
-                Position::AnyNTerm,
-                peptide.sequence().first().map(|p| p.aminoacid.aminoacid()),
-                &m,
-            )
-        });
-        let mut c_term = peptide.get_c_term().cloned().and_then(|m| {
-            find_replacement_modification(
-                self,
-                Position::AnyCTerm,
-                peptide.sequence().last().map(|p| p.aminoacid.aminoacid()),
-                &m,
-            )
-        });
+        let mut n_term = peptide
+            .get_n_term()
+            .iter()
+            .map(|m| {
+                find_replacement_modification(
+                    self,
+                    Position::AnyNTerm,
+                    peptide.sequence().first().map(|p| p.aminoacid.aminoacid()),
+                    m,
+                )
+                .unwrap_or_else(|| m.clone())
+            })
+            .collect_vec();
+        let mut c_term = peptide
+            .get_c_term()
+            .iter()
+            .map(|m| {
+                find_replacement_modification(
+                    self,
+                    Position::AnyCTerm,
+                    peptide.sequence().last().map(|p| p.aminoacid.aminoacid()),
+                    m,
+                )
+                .unwrap_or_else(|| m.clone())
+            })
+            .collect_vec();
         let len = peptide.len();
 
         // Go over all main stretch mods
@@ -330,13 +342,13 @@ impl PeptideModificationSearch {
                             is_n_term,
                             is_c_term,
                             Some(position.aminoacid.aminoacid()),
-                            &modification,
+                            modification,
                         ) {
-                            if location == Position::AnyNTerm && n_term.is_none() {
-                                n_term = Some(Modification::Simple(replace));
+                            if location == Position::AnyNTerm {
+                                n_term.push(Modification::Simple(replace));
                                 remove = Some(i);
-                            } else if location == Position::AnyCTerm && c_term.is_none() {
-                                c_term = Some(Modification::Simple(replace));
+                            } else if location == Position::AnyCTerm {
+                                c_term.push(Modification::Simple(replace));
                                 remove = Some(i);
                             } else if location == Position::Anywhere {
                                 *m = Modification::Simple(replace);
@@ -390,7 +402,7 @@ impl PeptideModificationSearch {
         }
     }
 
-    #[allow(clippy::missing_panics_doc, clippy::too_many_arguments)]
+    #[expect(clippy::missing_panics_doc, clippy::too_many_arguments)]
     fn find_replacement_uncached(
         mass_mode: MassMode,
         tolerance: Tolerance<Mass>,
@@ -474,17 +486,17 @@ impl PeptideModificationSearch {
 }
 
 #[test]
-#[allow(clippy::missing_panics_doc)]
+#[expect(clippy::missing_panics_doc)]
 fn test_replacement() {
     let mut search = PeptideModificationSearch::in_ontologies(vec![Ontology::Unimod], None)
         .replace_formulas(true);
-    let peptide = LinearPeptide::pro_forma("MSFNELT[79.9663]ESNKKSLM[+15.9949]E", None).unwrap();
-    let expected = LinearPeptide::pro_forma("MSFNELT[Phospho]ESNKKSLM[Oxidation]E", None).unwrap();
+    let peptide = Peptidoform::pro_forma("MSFNELT[79.9663]ESNKKSLM[+15.9949]E", None).unwrap();
+    let expected = Peptidoform::pro_forma("MSFNELT[Phospho]ESNKKSLM[Oxidation]E", None).unwrap();
     assert_eq!(search.search(peptide), expected);
-    let peptide = LinearPeptide::pro_forma("Q[-17.02655]NKKSLM[+15.9949]E", None).unwrap();
-    let expected = LinearPeptide::pro_forma("[Gln->pyro-glu]-QNKKSLM[Oxidation]E", None).unwrap();
+    let peptide = Peptidoform::pro_forma("Q[-17.02655]NKKSLM[+15.9949]E", None).unwrap();
+    let expected = Peptidoform::pro_forma("[Gln->pyro-glu]-QNKKSLM[Oxidation]E", None).unwrap();
     assert_eq!(search.search(peptide), expected);
-    let peptide = LinearPeptide::pro_forma("M[Formula:O1]KSLM[+15.9949]E", None).unwrap();
-    let expected = LinearPeptide::pro_forma("M[Oxidation]KSLM[Oxidation]E", None).unwrap();
+    let peptide = Peptidoform::pro_forma("M[Formula:O1]KSLM[+15.9949]E", None).unwrap();
+    let expected = Peptidoform::pro_forma("M[Oxidation]KSLM[Oxidation]E", None).unwrap();
     assert_eq!(search.search(peptide), expected);
 }
diff --git a/rustyms/src/peptide/mod.rs b/rustyms/src/peptidoform/mod.rs
similarity index 77%
rename from rustyms/src/peptide/mod.rs
rename to rustyms/src/peptidoform/mod.rs
index aec781f2..bde4853a 100644
--- a/rustyms/src/peptide/mod.rs
+++ b/rustyms/src/peptidoform/mod.rs
@@ -2,22 +2,22 @@
 
 mod annotated;
 mod complexity;
-mod compound_peptidoform;
+mod compound_peptidoform_ion;
 mod find_modifications;
-mod linear_peptide;
 mod parse;
 mod parse_modification;
 mod parse_sloppy;
 mod peptidoform;
+mod peptidoform_ion;
 #[cfg(test)]
 mod tests;
 mod validate;
 
 pub use annotated::*;
 pub use complexity::*;
-pub use compound_peptidoform::*;
+pub use compound_peptidoform_ion::*;
 pub use find_modifications::*;
-pub use linear_peptide::*;
 pub use parse_modification::*;
 pub use parse_sloppy::SloppyParsingParameters;
 pub use peptidoform::*;
+pub use peptidoform_ion::*;
diff --git a/rustyms/src/peptide/parse.rs b/rustyms/src/peptidoform/parse.rs
similarity index 84%
rename from rustyms/src/peptide/parse.rs
rename to rustyms/src/peptidoform/parse.rs
index d988c4e8..d263e56e 100644
--- a/rustyms/src/peptide/parse.rs
+++ b/rustyms/src/peptidoform/parse.rs
@@ -11,9 +11,10 @@ use crate::{
     },
     molecular_charge::MolecularCharge,
     ontologies::CustomDatabase,
-    peptide::Linked,
-    AminoAcid, CheckedAminoAcid, CompoundPeptidoform, Element, LinearPeptide, MolecularFormula,
-    Peptidoform, SequenceElement, SequencePosition,
+    peptidoform::Linked,
+    placement_rule::{PlacementRule, Position},
+    AminoAcid, CheckedAminoAcid, CompoundPeptidoformIon, Element, MolecularFormula, Peptidoform,
+    PeptidoformIon, SequenceElement, SequencePosition,
 };
 
 use super::{GlobalModification, Linear, ReturnModification, SemiAmbiguous};
@@ -26,13 +27,13 @@ enum End {
 }
 
 struct LinearPeptideResult {
-    peptide: LinearPeptide<Linear>,
+    peptide: Peptidoform<Linear>,
     index: usize,
     ending: End,
     cross_links: Vec<(usize, SequencePosition)>,
 }
 
-impl LinearPeptide<Linked> {
+impl Peptidoform<Linked> {
     /// Convenience wrapper to parse a linear peptide in ProForma notation, to handle all possible ProForma sequences look at [`CompoundPeptidoform::pro_forma`].
     /// # Errors
     /// It gives an error when the peptide is not correctly formatted. (Also see the `CompoundPeptidoform` main function for this.)
@@ -41,7 +42,7 @@ impl LinearPeptide<Linked> {
         value: &str,
         custom_database: Option<&CustomDatabase>,
     ) -> Result<Self, CustomError> {
-        CompoundPeptidoform::pro_forma(value, custom_database)?
+        CompoundPeptidoformIon::pro_forma(value, custom_database)?
             .singular()
             .ok_or_else(|| {
                 CustomError::error(
@@ -66,17 +67,16 @@ impl LinearPeptide<Linked> {
     }
 }
 
-impl Peptidoform {
+impl PeptidoformIon {
     /// Parse a peptidoform in the [ProForma specification](https://github.com/HUPO-PSI/ProForma).
     ///
     /// # Errors
     /// It fails when the string is not a valid ProForma string. Or when the string has multiple peptidoforms.
-    #[allow(clippy::too_many_lines)]
     pub fn pro_forma(
         value: &str,
         custom_database: Option<&CustomDatabase>,
     ) -> Result<Self, CustomError> {
-        CompoundPeptidoform::pro_forma(value, custom_database)?
+        CompoundPeptidoformIon::pro_forma(value, custom_database)?
             .singular()
             .ok_or_else(|| {
                 CustomError::error(
@@ -90,12 +90,11 @@ impl Peptidoform {
     }
 }
 
-impl CompoundPeptidoform {
+impl CompoundPeptidoformIon {
     /// Parse a compound peptidoform in the [ProForma specification](https://github.com/HUPO-PSI/ProForma).
     ///
     /// # Errors
     /// It fails when the string is not a valid ProForma string.
-    #[allow(clippy::too_many_lines)]
     pub fn pro_forma(
         value: &str,
         custom_database: Option<&CustomDatabase>,
@@ -134,7 +133,7 @@ impl CompoundPeptidoform {
         mut index: usize,
         global_modifications: &[GlobalModification],
         custom_database: Option<&CustomDatabase>,
-    ) -> Result<(Peptidoform, usize), CustomError> {
+    ) -> Result<(PeptidoformIon, usize), CustomError> {
         let mut peptides = Vec::new();
         let mut ending = End::CrossLink;
         let mut cross_link_lookup = Vec::new();
@@ -191,7 +190,7 @@ impl CompoundPeptidoform {
 
     /// # Errors
     /// It returns an error if the line is not a supported ProForma line.
-    #[allow(clippy::missing_panics_doc)] // Can not panic
+    #[expect(clippy::missing_panics_doc)] // Can not panic
     fn parse_linear_peptide(
         line: &str,
         mut index: usize,
@@ -205,7 +204,7 @@ impl CompoundPeptidoform {
                 Context::line(None, line, index, 1),
             ));
         }
-        let mut peptide = LinearPeptide::default();
+        let mut peptide = Peptidoform::default();
         let chars: &[u8] = line.as_bytes();
         let mut c_term = false;
         let mut ambiguous_aa_counter = std::num::NonZeroU32::MIN;
@@ -224,7 +223,7 @@ impl CompoundPeptidoform {
 
         // Unknown position mods
         if let Some(result) =
-            unknown_position_mods(chars, index, line, custom_database, &mut ambiguous_lookup)
+            global_unknown_position_mods(chars, index, line, custom_database, &mut ambiguous_lookup)
         {
             let (buf, mods) = result.map_err(|errors| {
                 CustomError::error(
@@ -252,31 +251,31 @@ impl CompoundPeptidoform {
                     "No valid closing delimiter, an N terminal modification should be closed by ']-'",
                     Context::line(None, line, index, 1),
                 ))?;
-            peptide.set_simple_n_term(
-                SimpleModificationInner::try_from(
-                    line,
-                    index + 1..end_index - 1,
-                    &mut ambiguous_lookup,
-                    cross_link_lookup,
-                    custom_database,
-                )
-                .map(|m| match m {
-                    ReturnModification::Defined(simple) => Some(simple),
-                    ReturnModification::CrossLinkReferenced(id) => {
-                        cross_link_found_positions.push((id, SequencePosition::NTerm));
-                        None
-                    }
-                    ReturnModification::Ambiguous(id, localisation_score, preferred) => {
-                        ambiguous_found_positions.push((
-                            SequencePosition::NTerm,
-                            preferred,
-                            id,
-                            localisation_score,
-                        ));
-                        None
-                    }
-                })?,
-            );
+            if let Some(m) = SimpleModificationInner::try_from(
+                line,
+                index + 1..end_index - 1,
+                &mut ambiguous_lookup,
+                cross_link_lookup,
+                custom_database,
+            )
+            .map(|m| match m.0 {
+                ReturnModification::Defined(simple) => Some(simple),
+                ReturnModification::CrossLinkReferenced(id) => {
+                    cross_link_found_positions.push((id, SequencePosition::NTerm));
+                    None
+                }
+                ReturnModification::Ambiguous(id, localisation_score, preferred) => {
+                    ambiguous_found_positions.push((
+                        SequencePosition::NTerm,
+                        preferred,
+                        id,
+                        localisation_score,
+                    ));
+                    None
+                }
+            })? {
+                peptide.add_simple_n_term(m);
+            }
             index = end_index + 1;
         }
 
@@ -342,7 +341,7 @@ impl CompoundPeptidoform {
                         let modification = SimpleModificationInner::try_from(
                             line, index + 1..end_index,
                             &mut ambiguous_lookup, cross_link_lookup, custom_database,
-                        )?.defined().ok_or_else(|| CustomError::error(
+                        )?.0.defined().ok_or_else(|| CustomError::error(
                             "Invalid ranged ambiguous modification",
                             "A ranged ambiguous modification has to be fully defined, so no ambiguous modification is allowed",
                             Context::line(None, line, index, 1),
@@ -377,16 +376,16 @@ impl CompoundPeptidoform {
                         "No valid closing delimiter",
                         Context::line(None, line, index, 1),
                     ))?;
-                    let modification = SimpleModificationInner::try_from(
+                    let (modification,_) = SimpleModificationInner::try_from(
                         line, index + 1..end_index,
                         &mut ambiguous_lookup, cross_link_lookup, custom_database,
                     )?;
                     let start_index = index +1;
                     index = end_index + 1;
                     if is_c_term {
-                        peptide = peptide.c_term(
+                        if let Some(m) =
                             match modification {
-                                ReturnModification::Defined(simple) => Ok(Some(Modification::Simple(simple))),
+                                ReturnModification::Defined(simple) => Ok(Some(simple)),
                                 ReturnModification::CrossLinkReferenced(id) =>
                                     {cross_link_found_positions.push((id, SequencePosition::CTerm)); Ok(None)},
                                 ReturnModification::Ambiguous(id, localisation_score, preferred) => {
@@ -398,7 +397,9 @@ impl CompoundPeptidoform {
                                     ));
                                     Ok(None)
                                 }
-                            }?);
+                            }? {
+                            peptide.add_simple_c_term(m);
+                        }
 
                         if index + 1 < chars.len() && chars[index] == b'/' && chars[index+1] != b'/' {
                             let (buf, charge_carriers) = parse_charge_state(line, index)?;
@@ -505,22 +506,25 @@ impl CompoundPeptidoform {
                 .map(|(index, _, _, score)| (*index, *score))
                 .collect_vec();
             let preferred = ambiguous.iter().find_map(|p| p.1.then_some(p.0));
-            if !peptide.add_ambiguous_modification(ambiguous_lookup[id].1.clone().ok_or_else(||
+            if !peptide.add_ambiguous_modification(ambiguous_lookup[id].modification.clone().ok_or_else(||
                 CustomError::error(
                     "Invalid ambiguous modification",
-                    format!("Ambiguous modification {} did not have a definition for the actual modification", ambiguous_lookup[id].0),
+                    format!("Ambiguous modification {} did not have a definition for the actual modification", ambiguous_lookup[id].name),
                     Context::full_line(0, line),
                 )
-                )?, Some(ambiguous_lookup[id].0.clone()), &positions, preferred) {
+                )?, Some(ambiguous_lookup[id].name.clone()), &positions, preferred, None,  true) {
                 return Err(CustomError::error(
                     "Modification of unknown position cannot be placed", 
-                    format!("There is no position where this ambiguous modification {} can be placed based on the placement rules in the database.", ambiguous_lookup[id].0),
+                    format!("There is no position where this ambiguous modification {} can be placed based on the placement rules in the database.", ambiguous_lookup[id].name),
                     Context::full_line(0, line),
                     ));
             }
         }
 
-        peptide.apply_unknown_position_modification(&unknown_position_modifications)?;
+        peptide.apply_unknown_position_modification(
+            &unknown_position_modifications,
+            &ambiguous_lookup,
+        )?;
         peptide
             .apply_ranged_unknown_position_modification(&ranged_unknown_position_modifications)?;
         peptide.enforce_modification_rules()?;
@@ -577,7 +581,7 @@ pub(super) fn global_modifications(
                 custom_database,
             )
             .map(|m| {
-                m.defined().ok_or_else(|| {
+                m.0.defined().ok_or_else(|| {
                     CustomError::error(
                         "Invalid global modification",
                         "A global modification cannot be ambiguous or a cross-linker",
@@ -586,71 +590,12 @@ pub(super) fn global_modifications(
                 })
             })
             .flat_err()?;
-            for aa in line[at_index..end_index].split(',') {
-                if aa.to_ascii_lowercase().starts_with("n-term") {
-                    if let Some((_, aa)) = aa.split_once(':') {
-                        global_modifications.push(GlobalModification::Fixed(
-                            crate::placement_rule::Position::AnyNTerm,
-                            Some(TryInto::<AminoAcid>::try_into(aa).map_err(|()| {
-                                CustomError::error(
-                                    "Invalid global modification",
-                                    "The location could not be read as an amino acid",
-                                    Context::line(
-                                        None,
-                                        line,
-                                        at_index + 7,
-                                        end_index - at_index - 7,
-                                    ),
-                                )
-                            })?),
-                            modification.clone(),
-                        ));
-                    } else {
-                        global_modifications.push(GlobalModification::Fixed(
-                            crate::placement_rule::Position::AnyNTerm,
-                            None,
-                            modification.clone(),
-                        ));
-                    }
-                } else if aa.to_ascii_lowercase().starts_with("c-term") {
-                    if let Some((_, aa)) = aa.split_once(':') {
-                        global_modifications.push(GlobalModification::Fixed(
-                            crate::placement_rule::Position::AnyCTerm,
-                            Some(TryInto::<AminoAcid>::try_into(aa).map_err(|()| {
-                                CustomError::error(
-                                    "Invalid global modification",
-                                    "The location could not be read as an amino acid",
-                                    Context::line(
-                                        None,
-                                        line,
-                                        at_index + 7,
-                                        end_index - at_index - 7,
-                                    ),
-                                )
-                            })?),
-                            modification.clone(),
-                        ));
-                    } else {
-                        global_modifications.push(GlobalModification::Fixed(
-                            crate::placement_rule::Position::AnyCTerm,
-                            None,
-                            modification.clone(),
-                        ));
-                    }
-                } else {
-                    global_modifications.push(GlobalModification::Fixed(
-                        crate::placement_rule::Position::Anywhere,
-                        Some(TryInto::<AminoAcid>::try_into(aa).map_err(|()| {
-                            CustomError::error(
-                                "Invalid global modification",
-                                "The location could not be read as an amino acid",
-                                Context::line(None, line, at_index, end_index - at_index),
-                            )
-                        })?),
-                        modification.clone(),
-                    ));
-                }
-            }
+            let rules = parse_placement_rules(line, at_index..end_index)?;
+            global_modifications.extend(
+                rules
+                    .into_iter()
+                    .map(|r| GlobalModification::Fixed(r, modification.clone())),
+            );
         } else if &line[index + 1..end_index].to_ascii_lowercase() == "d" {
             global_modifications.push(GlobalModification::Isotope(Element::H, NonZeroU16::new(2)));
         } else {
@@ -696,21 +641,74 @@ pub(super) fn global_modifications(
     Ok((index, global_modifications))
 }
 
-/// A list of found modifications
-type UnknownPositionMods = (usize, Vec<SimpleModification>);
+/// Parse a set of placement rules.
+/// # Errors
+/// When any rule is invalid.
+pub fn parse_placement_rules(
+    line: &str,
+    range: std::ops::Range<usize>,
+) -> Result<Vec<PlacementRule>, CustomError> {
+    let mut result = Vec::new();
+    for aa in line[range.clone()].split(',') {
+        if aa.to_ascii_lowercase().starts_with("n-term") {
+            if let Some((_, aa)) = aa.split_once(':') {
+                result.push(PlacementRule::AminoAcid(
+                    vec![TryInto::<AminoAcid>::try_into(aa).map_err(|()| {
+                        CustomError::error(
+                            "Invalid global modification",
+                            "The location could not be read as an amino acid",
+                            Context::line(None, line, range.start, range.len()),
+                        )
+                    })?],
+                    Position::AnyNTerm,
+                ));
+            } else {
+                result.push(PlacementRule::Terminal(Position::AnyNTerm));
+            }
+        } else if aa.to_ascii_lowercase().starts_with("c-term") {
+            if let Some((_, aa)) = aa.split_once(':') {
+                result.push(PlacementRule::AminoAcid(
+                    vec![TryInto::<AminoAcid>::try_into(aa).map_err(|()| {
+                        CustomError::error(
+                            "Invalid global modification",
+                            "The location could not be read as an amino acid",
+                            Context::line(None, line, range.start, range.len()),
+                        )
+                    })?],
+                    Position::AnyCTerm,
+                ));
+            } else {
+                result.push(PlacementRule::Terminal(Position::AnyCTerm));
+            }
+        } else {
+            result.push(PlacementRule::AminoAcid(
+                vec![TryInto::<AminoAcid>::try_into(aa).map_err(|()| {
+                    CustomError::error(
+                        "Invalid global modification",
+                        "The location could not be read as an amino acid",
+                        Context::line(None, line, range.start, range.len()),
+                    )
+                })?],
+                Position::Anywhere,
+            ));
+        }
+    }
+    Ok(result)
+}
+
 /// If the text is recognised as a unknown mods list it is Some(..), if it has errors during parsing Some(Err(..))
 /// The returned happy path contains the mods and the index from where to continue parsing.
 /// # Errors
 /// Give all errors when the text cannot be read as mods of unknown position.
 /// # Panics
 /// Breaks if the text is not valid UTF-8
-pub(super) fn unknown_position_mods(
+pub(super) fn global_unknown_position_mods(
     chars: &[u8],
     start: usize,
     line: &str,
     custom_database: Option<&CustomDatabase>,
     ambiguous_lookup: &mut AmbiguousLookup,
-) -> Option<Result<UnknownPositionMods, Vec<CustomError>>> {
+) -> Option<Result<(usize, Vec<usize>), Vec<CustomError>>> {
     let mut index = start;
     let mut modifications = Vec::new();
     let mut errs = Vec::new();
@@ -720,16 +718,27 @@ pub(super) fn unknown_position_mods(
     while chars.get(index) == Some(&b'[') {
         let start_index = index;
         index = next_char(chars, index + 1, b']')? + 1;
-        let modification = match SimpleModificationInner::try_from(
+        let id = match SimpleModificationInner::try_from(
             std::str::from_utf8(chars).unwrap(),
             start_index + 1..index - 1,
             ambiguous_lookup,
             &mut cross_link_lookup,
             custom_database,
         ) {
-            Ok(ReturnModification::Defined(m)) => m,
-            Ok(ReturnModification::Ambiguous(_, _, _)) => continue, // Added to list and that is the only thing to do
-            Ok(ReturnModification::CrossLinkReferenced(_)) => {
+            Ok((ReturnModification::Defined(m), settings)) => {
+                let id = ambiguous_lookup.len();
+                ambiguous_lookup.push(crate::modification::AmbiguousLookupEntry::new(
+                    format!("u{id}"),
+                    Some(m),
+                ));
+                ambiguous_lookup[id].copy_settings(&settings);
+                id
+            }
+            Ok((ReturnModification::Ambiguous(id, _, _), settings)) => {
+                ambiguous_lookup[id].copy_settings(&settings);
+                id
+            }
+            Ok((ReturnModification::CrossLinkReferenced(_), _)) => {
                 errs.push(CustomError::error(
                     "Invalid unknown position modification",
                     "A modification of unknown position cannot be a cross-link",
@@ -764,7 +773,17 @@ pub(super) fn unknown_position_mods(
         } else {
             1
         };
-        modifications.extend(std::iter::repeat(modification).take(number));
+        if number > 1 {
+            let group_name = ambiguous_lookup.len();
+            ambiguous_lookup[id].group = Some(group_name);
+            modifications.push(id);
+            for _ in 0..number {
+                modifications.push(ambiguous_lookup.len());
+                ambiguous_lookup.push(ambiguous_lookup[id].clone());
+            }
+        } else {
+            modifications.push(id);
+        }
     }
     if chars.get(index) == Some(&b'?') {
         Some(if errs.is_empty() {
@@ -806,7 +825,7 @@ fn labile_modifications(
                 custom_database,
             )
             .and_then(|m| {
-                m.defined().ok_or_else(|| {
+                m.0.defined().ok_or_else(|| {
                     CustomError::error(
                         "Invalid labile modification",
                         "A labile modification cannot be ambiguous or a cross-linker",
diff --git a/rustyms/src/peptide/parse_modification.rs b/rustyms/src/peptidoform/parse_modification.rs
similarity index 74%
rename from rustyms/src/peptide/parse_modification.rs
rename to rustyms/src/peptidoform/parse_modification.rs
index 4ad8b54d..6587feff 100644
--- a/rustyms/src/peptide/parse_modification.rs
+++ b/rustyms/src/peptidoform/parse_modification.rs
@@ -1,6 +1,9 @@
-use crate::modification::{
-    AmbiguousLookup, CrossLinkLookup, CrossLinkName, Ontology, SimpleModification,
-    SimpleModificationInner,
+use crate::{
+    modification::{
+        AmbiguousLookup, AmbiguousLookupEntry, CrossLinkLookup, CrossLinkName, Ontology,
+        SimpleModification, SimpleModificationInner,
+    },
+    placement_rule::PlacementRule,
 };
 use ordered_float::OrderedFloat;
 use serde::{Deserialize, Serialize};
@@ -18,9 +21,8 @@ use crate::{
     glycan::{GlycanStructure, MonoSaccharide},
     helper_functions::*,
     ontologies::CustomDatabase,
-    placement_rule::Position,
-    system::{dalton, Mass, OrderedMass},
-    AminoAcid, Element, MolecularFormula,
+    system::{dalton, Mass},
+    Element, MolecularFormula,
 };
 
 impl SimpleModificationInner {
@@ -35,39 +37,50 @@ impl SimpleModificationInner {
         ambiguous_lookup: &mut AmbiguousLookup,
         cross_link_lookup: &mut CrossLinkLookup,
         custom_database: Option<&CustomDatabase>,
-    ) -> Result<ReturnModification, CustomError> {
+    ) -> Result<(ReturnModification, MUPSettings), CustomError> {
         // Because multiple modifications could be chained with the pipe operator
         // the parsing iterates over all links until it finds one it understands
         // it then returns that one. If no 'understandable' links are found it
         // returns the last link, if this is an info it returns a mass shift of 0,
         // but if any of the links returned an error it returns the last error.
-        let mut last_result = Ok(None);
+        let mut modification = None;
+        let mut settings = MUPSettings::default();
         let mut last_error = None;
         let mut offset = range.start;
         for part in line[range].split('|') {
-            last_result = parse_single_modification(
+            match parse_single_modification(
                 line,
                 part,
                 offset,
                 ambiguous_lookup,
                 cross_link_lookup,
                 custom_database,
-            );
-            if let Ok(Some(m)) = last_result {
-                return Ok(m);
-            }
-            if let Err(er) = &last_result {
-                last_error = Some(er.clone());
+            ) {
+                Ok(SingleReturnModification::None) => (),
+                Ok(SingleReturnModification::Modification(m)) => modification = Some(m),
+                Ok(SingleReturnModification::Positions(p)) => settings.position = Some(p),
+                Ok(SingleReturnModification::Limit(l)) => settings.limit = Some(l),
+                Ok(SingleReturnModification::ColocalisePlacedModifications(s)) => {
+                    settings.colocalise_placed_modifications = s;
+                }
+                Ok(SingleReturnModification::ColocaliseModificationsOfUnknownPosition(s)) => {
+                    settings.colocalise_modifications_of_unknown_position = s;
+                }
+                Err(e) => last_error = Some(e),
             }
             offset += part.len() + 1;
         }
+        if let Some(ReturnModification::Ambiguous(id, _, true)) = &modification {
+            ambiguous_lookup[*id].copy_settings(&settings);
+        }
         last_error.map_or_else(
             || {
-                last_result.map(|m| {
-                    m.unwrap_or_else(|| {
-                        ReturnModification::Defined(Arc::new(Self::Mass(OrderedMass::zero())))
-                    })
-                })
+                Ok((
+                    modification.unwrap_or(ReturnModification::Defined(Arc::new(Self::Mass(
+                        Mass::default().into(),
+                    )))),
+                    settings,
+                ))
             },
             Err,
         )
@@ -76,9 +89,42 @@ impl SimpleModificationInner {
 
 static MOD_REGEX: OnceLock<Regex> = OnceLock::new();
 
+enum SingleReturnModification {
+    None,
+    Modification(ReturnModification),
+    Positions(Vec<PlacementRule>),
+    Limit(usize),
+    ColocalisePlacedModifications(bool),
+    ColocaliseModificationsOfUnknownPosition(bool),
+}
+
+/// Settings for a modification of unknown position
+#[derive(Clone, PartialEq, Eq, PartialOrd, Ord, Hash, Debug, Serialize, Deserialize)]
+pub struct MUPSettings {
+    /// The additional placement rules
+    pub(crate) position: Option<Vec<PlacementRule>>,
+    /// The maximal number for a grouped mup (^x)
+    pub(crate) limit: Option<usize>,
+    /// Allow this mup to colocalise with placed modifications
+    pub(crate) colocalise_placed_modifications: bool,
+    /// Allow this mup to colocalise with other mups
+    pub(crate) colocalise_modifications_of_unknown_position: bool,
+}
+
+impl std::default::Default for MUPSettings {
+    fn default() -> Self {
+        Self {
+            position: None,
+            limit: None,
+            colocalise_placed_modifications: true,
+            colocalise_modifications_of_unknown_position: true,
+        }
+    }
+}
+
 /// # Errors
 /// It returns an error when the given line cannot be read as a single modification.
-#[allow(clippy::missing_panics_doc)]
+#[expect(clippy::missing_panics_doc)]
 fn parse_single_modification(
     line: &str,
     full_modification: &str,
@@ -86,7 +132,7 @@ fn parse_single_modification(
     ambiguous_lookup: &mut AmbiguousLookup,
     cross_link_lookup: &mut CrossLinkLookup,
     custom_database: Option<&CustomDatabase>,
-) -> Result<Option<ReturnModification>, CustomError> {
+) -> Result<SingleReturnModification, CustomError> {
     // Parse the whole intricate structure of the single modification (see here in action: https://regex101.com/r/pW5gsj/1)
     let regex = MOD_REGEX.get_or_init(|| {
         Regex::new(r"^(([^:#]*)(?::([^#]+))?)(?:#([0-9A-Za-z]+)(?:\((\d+\.\d+)\))?)?$").unwrap()
@@ -254,13 +300,11 @@ fn parse_single_modification(
                             .with_long_description("This modification cannot be read as a GNO name")
                     }),
                 ("formula", tail) => Ok(Some(Arc::new(SimpleModificationInner::Formula(
-                    MolecularFormula::from_pro_forma(tail, .., false, false, true).map_err(
-                        |e| {
-                            basic_error.with_long_description(format!(
-                                "This modification cannot be read as a valid formula: {e}"
-                            ))
-                        },
-                    )?,
+                    MolecularFormula::from_pro_forma(tail, .., true, false, true).map_err(|e| {
+                        basic_error.with_long_description(format!(
+                            "This modification cannot be read as a valid formula: {e}"
+                        ))
+                    })?,
                 )))),
                 ("glycan", tail) => Ok(Some(Arc::new(SimpleModificationInner::Glycan(
                     MonoSaccharide::from_composition(tail)
@@ -277,6 +321,45 @@ fn parse_single_modification(
                         "This modification cannot be read as a numerical modification",
                     )
                 }),
+                ("position", tail) => {
+                    match super::parse::parse_placement_rules(tail, 0..tail.len()).map_err(
+                        |error| basic_error.with_long_description(error.long_description()),
+                    ) {
+                        Ok(rules) => return Ok(SingleReturnModification::Positions(rules)),
+                        Err(e) => Err(e),
+                    }
+                }
+                ("limit", tail) => {
+                    match tail.parse::<usize>().map_err(|error| {
+                        basic_error.with_long_description(format!(
+                            "Invalid limit for modification of unknown position, the number is {}",
+                            explain_number_error(&error)
+                        ))
+                    }) {
+                        Ok(l) => return Ok(SingleReturnModification::Limit(l)),
+                        Err(e) => Err(e),
+                    }
+                }
+                ("colocaliseplacedmodifications", tail) => {
+                    match tail.parse::<bool>().map_err(|error| {
+                        basic_error.with_long_description(format!(
+                            "Invalid setting for colocalise placed modifications for modification of unknown position, the boolean is {error}",
+                        ))
+                    }) {
+                        Ok(s) => return Ok(SingleReturnModification::ColocalisePlacedModifications(s)),
+                        Err(e) => Err(e),
+                    }
+                }
+                ("colocalisemodificationsofunknownposition", tail) => {
+                    match tail.parse::<bool>().map_err(|error| {
+                        basic_error.with_long_description(format!(
+                            "Invalid setting for colocalise modifications of unknown position for modification of unknown position, the boolean is {error}",
+                        ))
+                    }) {
+                        Ok(s) => return Ok(SingleReturnModification::ColocaliseModificationsOfUnknownPosition(s)),
+                        Err(e) => Err(e),
+                    }
+                }
                 (_, _) => Ontology::Unimod
                     .find_name(full.0, custom_database)
                     .or_else(|| Ontology::Psimod.find_name(full.0, custom_database))
@@ -321,7 +404,7 @@ fn parse_single_modification(
         };
 
         if let Some(group) = label_group {
-            if group.0.to_ascii_lowercase() == "branch" {
+            if group.0.eq_ignore_ascii_case("branch") {
                 let index = cross_link_lookup
                     .iter()
                     .position(|c| c.0 == CrossLinkName::Branch)
@@ -347,7 +430,9 @@ fn parse_single_modification(
                     }
                     cross_link_lookup[index].1 = Some(linker);
                 }
-                Ok(Some(ReturnModification::CrossLinkReferenced(index)))
+                Ok(SingleReturnModification::Modification(
+                    ReturnModification::CrossLinkReferenced(index),
+                ))
             } else if let Some(name) = group.0.to_ascii_lowercase().strip_prefix("xl") {
                 let name = CrossLinkName::Name(name.to_string());
                 let index = cross_link_lookup
@@ -375,7 +460,9 @@ fn parse_single_modification(
                     }
                     cross_link_lookup[index].1 = Some(linker);
                 }
-                Ok(Some(ReturnModification::CrossLinkReferenced(index)))
+                Ok(SingleReturnModification::Modification(
+                    ReturnModification::CrossLinkReferenced(index),
+                ))
             } else {
                 handle_ambiguous_modification(
                     modification,
@@ -386,7 +473,11 @@ fn parse_single_modification(
                 )
             }
         } else {
-            modification.map(|m| m.map(ReturnModification::Defined))
+            modification.map(|m| {
+                m.map_or(SingleReturnModification::None, |m| {
+                    SingleReturnModification::Modification(ReturnModification::Defined(m))
+                })
+            })
         }
     } else {
         Err(CustomError::error(
@@ -406,14 +497,14 @@ fn handle_ambiguous_modification(
     localisation_score: Option<OrderedFloat<f64>>,
     ambiguous_lookup: &mut AmbiguousLookup,
     context: Context,
-) -> Result<Option<ReturnModification>, CustomError> {
+) -> Result<SingleReturnModification, CustomError> {
     let group_name = group.0.to_ascii_lowercase();
     // Search for a previous definition of this name, store as Some((index, modification_definition_present)) or None if there is no definition in place
     let found_definition = ambiguous_lookup
         .iter()
         .enumerate()
-        .find(|(_, (name, _))| name == &group_name)
-        .map(|(index, (_, modification))| (index, modification.is_some()));
+        .find(|(_, entry)| entry.name == group_name)
+        .map(|(index, entry)| (index, entry.modification.is_some()));
     // Handle all possible cases of having a modification found at this position and having a modification defined in the ambiguous lookup
     match (modification, found_definition) {
         // Have a mod defined here and already in the lookup (error)
@@ -425,17 +516,17 @@ fn handle_ambiguous_modification(
             )),
         // Have a mod defined here, the name present in the lookup but not yet the mod
         (Ok(Some(m)), Some((index, false))) => {
-            ambiguous_lookup[index].1 = Some(m);
-            Ok(Some(ReturnModification::Ambiguous(index, localisation_score, true)))
+            ambiguous_lookup[index].modification = Some(m);
+            Ok(SingleReturnModification::Modification(ReturnModification::Ambiguous(index, localisation_score, true)))
         },
         // No mod defined, but the name is present in the lookup
-        (Ok(None), Some((index, _))) => Ok(Some(ReturnModification::Ambiguous(index, localisation_score, false))),
+        (Ok(None), Some((index, _))) => Ok(SingleReturnModification::Modification(ReturnModification::Ambiguous(index, localisation_score, false))),
         // The mod is not already in the lookup
         (Ok(m), None) => {
             let index = ambiguous_lookup.len();
             let preferred = m.is_some();
-            ambiguous_lookup.push((group_name, m));
-            Ok(Some(ReturnModification::Ambiguous(index, localisation_score, preferred)))
+            ambiguous_lookup.push(AmbiguousLookupEntry::new(group_name, m));
+            Ok(SingleReturnModification::Modification(ReturnModification::Ambiguous(index, localisation_score, preferred)))
         },
         // Earlier error
         (Err(e), _) => Err(e),
@@ -470,7 +561,7 @@ pub enum GlobalModification {
     /// A global isotope modification
     Isotope(Element, Option<NonZeroU16>),
     /// Can be placed on any place it fits, if that is the correct aminoacid and it fits according to the placement rules of the modification itself
-    Fixed(Position, Option<AminoAcid>, SimpleModification),
+    Fixed(PlacementRule, SimpleModification),
 }
 
 /// # Errors
diff --git a/rustyms/src/peptide/parse_sloppy.rs b/rustyms/src/peptidoform/parse_sloppy.rs
similarity index 96%
rename from rustyms/src/peptide/parse_sloppy.rs
rename to rustyms/src/peptidoform/parse_sloppy.rs
index d4b0ed5e..ed7d4398 100644
--- a/rustyms/src/peptide/parse_sloppy.rs
+++ b/rustyms/src/peptidoform/parse_sloppy.rs
@@ -10,7 +10,7 @@ use crate::{
     helper_functions::{end_of_enclosure, parse_named_counter, ResultExtensions},
     modification::{Modification, Ontology, SimpleModification, SimpleModificationInner},
     ontologies::CustomDatabase,
-    peptide::*,
+    peptidoform::*,
     system::Mass,
     AminoAcid, SequenceElement,
 };
@@ -31,7 +31,7 @@ pub struct SloppyParsingParameters {
     pub replace_mass_modifications: Option<Vec<SimpleModification>>,
 }
 
-impl LinearPeptide<SemiAmbiguous> {
+impl Peptidoform<SemiAmbiguous> {
     /// Read sloppy ProForma like sequences. Defined by the use of square or round braces to indicate
     /// modifications and missing any particular method of defining the N or C terminal modifications.
     /// Additionally any underscores will be ignored both on the ends and inside the sequence.
@@ -41,7 +41,7 @@ impl LinearPeptide<SemiAmbiguous> {
     ///
     /// # Errors
     /// If it does not fit the above description.
-    #[allow(clippy::missing_panics_doc)] // Cannot panic
+    #[expect(clippy::missing_panics_doc)] // Cannot panic
     pub fn sloppy_pro_forma(
         line: &str,
         location: std::ops::Range<usize>,
@@ -91,7 +91,7 @@ impl LinearPeptide<SemiAmbiguous> {
                     index = end_index + 1;
 
                     let pep_len = peptide.len();
-                    let n_term_mod = peptide.get_n_term().is_some();
+                    let n_term_empty = peptide.get_n_term().is_empty();
                     match peptide.sequence_mut().last_mut() {
                         Some(aa) => {
                             if pep_len == 1
@@ -101,27 +101,27 @@ impl LinearPeptide<SemiAmbiguous> {
                                 && modification
                                     .is_possible(aa, crate::SequencePosition::NTerm)
                                     .any_possible()
-                                && !n_term_mod
+                                && n_term_empty
                             {
-                                peptide.set_simple_n_term(Some(
+                                peptide.add_simple_n_term(
                                     modification
                                         .simple()
                                         .expect(
                                             "Can only put a simple modification on an N terminus.",
                                         )
                                         .clone(),
-                                ));
+                                );
                             } else {
                                 aa.modifications.push(modification);
                             }
                         }
                         None => {
-                            peptide.set_simple_n_term(Some(
+                            peptide.add_simple_n_term(
                                 modification
                                     .simple()
                                     .expect("Can only put a simple modification on an N terminus.")
                                     .clone(),
-                            ));
+                            );
                         }
                     }
                 }
@@ -178,7 +178,7 @@ impl LinearPeptide<SemiAmbiguous> {
                     match peptide.sequence_mut().last_mut() {
                         Some(aa) => aa.modifications.push(Modification::Simple(modification)),
                         None => {
-                            peptide.set_simple_n_term(Some(modification));
+                            peptide.add_simple_n_term(modification);
                         }
                     }
                     index += length;
@@ -235,7 +235,7 @@ impl Modification {
     /// # Errors
     /// If the name is not in Unimod, PSI-MOD, the custom database, or the predefined list of common trivial names.
     /// Or if this is the case when the modification follows a known structure (eg `mod (AAs)`).
-    #[allow(clippy::missing_panics_doc)]
+    #[expect(clippy::missing_panics_doc)]
     pub fn sloppy_modification(
         line: &str,
         location: std::ops::Range<usize>,
@@ -319,7 +319,7 @@ impl Modification {
                 },
                 None,
             ), // pyro Glu with the logic to pick the correct modification based on the amino acid it is placed on
-            _ => crate::peptide::parse_modification::numerical_mod(&name)
+            _ => crate::peptidoform::parse_modification::numerical_mod(&name)
                 .ok()
                 .or_else(|| Ontology::Unimod.find_name(&name, custom_database))
                 .or_else(|| Ontology::Psimod.find_name(&name, custom_database))
diff --git a/rustyms/src/peptide/linear_peptide.rs b/rustyms/src/peptidoform/peptidoform.rs
similarity index 73%
rename from rustyms/src/peptide/linear_peptide.rs
rename to rustyms/src/peptidoform/peptidoform.rs
index 85b1fddf..9aeb1461 100644
--- a/rustyms/src/peptide/linear_peptide.rs
+++ b/rustyms/src/peptidoform/peptidoform.rs
@@ -10,7 +10,7 @@ use crate::{
         SimpleModificationInner,
     },
     molecular_charge::{CachedCharge, MolecularCharge},
-    peptide::*,
+    peptidoform::*,
     placement_rule::PlacementRule,
     system::usize::Charge,
     AmbiguousLabel, DiagnosticIon, Element, Model, MolecularFormula, Multi, MultiChemical,
@@ -85,44 +85,57 @@ use std::{
 /// ```
 ///
 #[derive(PartialOrd, Ord, Debug, Serialize, Deserialize)]
-pub struct LinearPeptide<Complexity> {
+pub struct Peptidoform<Complexity> {
     /// Global isotope modifications, saved as the element and the species that
     /// all occurrence of that element will consist of. For example (N, 15) will
     /// make all occurring nitrogen atoms be isotope 15.
     global: Vec<(Element, Option<NonZeroU16>)>,
     /// Labile modifications, which will not be found in the actual spectrum.
     labile: Vec<SimpleModification>,
-    /// N terminal modification
-    n_term: Option<Modification>,
-    /// C terminal modification
-    c_term: Option<Modification>,
+    /// N terminal modifications
+    n_term: Vec<Modification>,
+    /// C terminal modifications
+    c_term: Vec<Modification>,
     /// The sequence of this peptide (includes local modifications)
     sequence: Vec<SequenceElement<Complexity>>,
     /// For each ambiguous modification list all possible positions it can be placed on.
     /// Indexed by the ambiguous modification id.
-    ambiguous_modifications: Vec<Vec<SequencePosition>>,
+    modifications_of_unknown_position: Vec<AmbiguousEntry>,
     /// The adduct ions, if specified
     charge_carriers: Option<MolecularCharge>,
     /// The marker indicating which level of complexity this peptide (potentially) uses
     marker: PhantomData<Complexity>,
 }
 
-impl<Complexity> Default for LinearPeptide<Complexity> {
+/// An entry in the ambiguous lookup
+#[derive(PartialOrd, Ord, Debug, Serialize, Deserialize, Eq, PartialEq, Clone, Hash)]
+struct AmbiguousEntry {
+    /// The allowed locations for this modification
+    positions: Vec<SequencePosition>,
+    /// The maximal number of this modification on one place
+    limit: Option<usize>,
+    /// Determines if this modification can colocalise with other modifications of unknown position
+    colocalise_modifications_of_unknown_position: bool,
+    /// Group, used for '^x'  
+    group: Option<usize>,
+}
+
+impl<Complexity> Default for Peptidoform<Complexity> {
     fn default() -> Self {
         Self {
             global: Vec::new(),
             labile: Vec::new(),
-            n_term: None,
-            c_term: None,
+            n_term: Vec::new(),
+            c_term: Vec::new(),
             sequence: Vec::new(),
-            ambiguous_modifications: Vec::new(),
+            modifications_of_unknown_position: Vec::new(),
             charge_carriers: None,
             marker: PhantomData,
         }
     }
 }
 
-impl<Complexity> Clone for LinearPeptide<Complexity> {
+impl<Complexity> Clone for Peptidoform<Complexity> {
     fn clone(&self) -> Self {
         Self {
             global: self.global.clone(),
@@ -130,43 +143,43 @@ impl<Complexity> Clone for LinearPeptide<Complexity> {
             n_term: self.n_term.clone(),
             c_term: self.c_term.clone(),
             sequence: self.sequence.clone(),
-            ambiguous_modifications: self.ambiguous_modifications.clone(),
+            modifications_of_unknown_position: self.modifications_of_unknown_position.clone(),
             charge_carriers: self.charge_carriers.clone(),
             marker: PhantomData,
         }
     }
 }
 
-impl<OwnComplexity, OtherComplexity> PartialEq<LinearPeptide<OtherComplexity>>
-    for LinearPeptide<OwnComplexity>
+impl<OwnComplexity, OtherComplexity> PartialEq<Peptidoform<OtherComplexity>>
+    for Peptidoform<OwnComplexity>
 {
-    fn eq(&self, other: &LinearPeptide<OtherComplexity>) -> bool {
+    fn eq(&self, other: &Peptidoform<OtherComplexity>) -> bool {
         self.global == other.global
             && self.labile == other.labile
             && self.n_term == other.n_term
             && self.c_term == other.c_term
             && self.sequence == other.sequence
-            && self.ambiguous_modifications == other.ambiguous_modifications
+            && self.modifications_of_unknown_position == other.modifications_of_unknown_position
             && self.charge_carriers == other.charge_carriers
     }
 }
 
-impl<Complexity> std::hash::Hash for LinearPeptide<Complexity> {
+impl<Complexity> std::hash::Hash for Peptidoform<Complexity> {
     fn hash<H: std::hash::Hasher>(&self, state: &mut H) {
         self.global.hash(state);
         self.labile.hash(state);
         self.n_term.hash(state);
         self.c_term.hash(state);
         self.sequence.hash(state);
-        self.ambiguous_modifications.hash(state);
+        self.modifications_of_unknown_position.hash(state);
         self.charge_carriers.hash(state);
     }
 }
 
-impl<Complexity> Eq for LinearPeptide<Complexity> {}
+impl<Complexity> Eq for Peptidoform<Complexity> {}
 
 /// Implement the complexity checks to reduce the complexity of a peptide in a controlled fashion.
-impl<Complexity> LinearPeptide<Complexity> {
+impl<Complexity> Peptidoform<Complexity> {
     /// Check if this peptide does not use any of the features reserved for [`Linked`].
     ///
     /// This checks if all modifications (in the sequence and the termini) are [`SimpleModification`]s.
@@ -174,12 +187,12 @@ impl<Complexity> LinearPeptide<Complexity> {
         self.sequence()
             .iter()
             .all(|seq| seq.modifications.iter().all(|m| !m.is_cross_link()))
-            && self.n_term.as_ref().map_or(true, |n| !n.is_cross_link())
-            && self.c_term.as_ref().map_or(true, |c| !c.is_cross_link())
+            && self.n_term.iter().all(|n| !n.is_cross_link())
+            && self.c_term.iter().all(|c| !c.is_cross_link())
     }
 
     /// Convert this peptide into [`Linear`].
-    pub fn into_linear(self) -> Option<LinearPeptide<Linear>> {
+    pub fn into_linear(self) -> Option<Peptidoform<Linear>> {
         if self.is_linear() {
             Some(self.mark())
         } else {
@@ -199,7 +212,7 @@ impl<Complexity> LinearPeptide<Complexity> {
     }
 
     /// Convert this peptide into [`SimpleLinear`].
-    pub fn into_simple_linear(self) -> Option<LinearPeptide<SimpleLinear>> {
+    pub fn into_simple_linear(self) -> Option<Peptidoform<SimpleLinear>> {
         if self.is_simple_linear() {
             Some(self.mark())
         } else {
@@ -213,12 +226,12 @@ impl<Complexity> LinearPeptide<Complexity> {
     /// This checks if this peptide does not have any ambiguous modifications or amino acids (`(?AA)` in ProForma).
     pub fn is_semi_ambiguous(&self) -> bool {
         self.is_simple_linear()
-            && self.ambiguous_modifications.is_empty()
+            && self.modifications_of_unknown_position.is_empty()
             && !self.sequence.iter().any(|seq| seq.ambiguous.is_some())
     }
 
     /// Convert this peptide into [`SemiAmbiguous`].
-    pub fn into_semi_ambiguous(self) -> Option<LinearPeptide<SemiAmbiguous>> {
+    pub fn into_semi_ambiguous(self) -> Option<Peptidoform<SemiAmbiguous>> {
         if self.is_semi_ambiguous() {
             Some(self.mark())
         } else {
@@ -239,7 +252,7 @@ impl<Complexity> LinearPeptide<Complexity> {
     }
 
     /// Convert this peptide into [`UnAmbiguous`].
-    pub fn into_unambiguous(self) -> Option<LinearPeptide<UnAmbiguous>> {
+    pub fn into_unambiguous(self) -> Option<Peptidoform<UnAmbiguous>> {
         if self.is_unambiguous() {
             Some(self.mark())
         } else {
@@ -248,13 +261,13 @@ impl<Complexity> LinearPeptide<Complexity> {
     }
 }
 
-impl<Complexity: HighestOf<Linear>> LinearPeptide<Complexity> {
+impl<Complexity: HighestOf<Linear>> Peptidoform<Complexity> {
     /// Add global isotope modifications, if any is invalid it returns None
     #[must_use]
     pub fn global(
         mut self,
         global: impl IntoIterator<Item = (Element, Option<NonZeroU16>)>,
-    ) -> Option<LinearPeptide<Complexity::HighestLevel>> {
+    ) -> Option<Peptidoform<Complexity::HighestLevel>> {
         for modification in global {
             if modification.0.is_valid(modification.1) {
                 self.global.push(modification);
@@ -270,16 +283,16 @@ impl<Complexity: HighestOf<Linear>> LinearPeptide<Complexity> {
     pub fn labile(
         mut self,
         labile: impl IntoIterator<Item = SimpleModification>,
-    ) -> LinearPeptide<Complexity::HighestLevel> {
+    ) -> Peptidoform<Complexity::HighestLevel> {
         self.labile.extend(labile);
         self.mark::<Complexity::HighestLevel>()
     }
 }
 
-impl<Complexity> LinearPeptide<Complexity> {
+impl<Complexity> Peptidoform<Complexity> {
     /// Mark this peptide with the following complexity, be warned that the complexity level is not checked.
-    pub(super) fn mark<M>(self) -> LinearPeptide<M> {
-        LinearPeptide {
+    pub(super) fn mark<M>(self) -> Peptidoform<M> {
+        Peptidoform {
             global: self.global,
             labile: self.labile,
             n_term: self.n_term,
@@ -289,7 +302,7 @@ impl<Complexity> LinearPeptide<Complexity> {
                 .into_iter()
                 .map(SequenceElement::mark)
                 .collect(),
-            ambiguous_modifications: self.ambiguous_modifications,
+            modifications_of_unknown_position: self.modifications_of_unknown_position,
             charge_carriers: self.charge_carriers,
             marker: PhantomData,
         }
@@ -298,7 +311,7 @@ impl<Complexity> LinearPeptide<Complexity> {
     /// Cast a linear peptide into a more complex linear peptide. This undoes any work done by
     /// functions like [`Self::into_linear`]. This does not change the content of the linear
     /// peptide. It only allows to pass this as higher complexity if needed.
-    pub fn cast<NewComplexity: AtLeast<Complexity>>(self) -> LinearPeptide<NewComplexity> {
+    pub fn cast<NewComplexity: AtLeast<Complexity>>(self) -> Peptidoform<NewComplexity> {
         self.mark()
     }
 
@@ -323,20 +336,30 @@ impl<Complexity> LinearPeptide<Complexity> {
         &mut self.sequence
     }
 
-    /// Add the N terminal modification
+    /// Set the N terminal modifications
     #[must_use]
-    pub fn n_term(mut self, term: Option<Modification>) -> Self {
+    pub fn n_term(mut self, term: Vec<Modification>) -> Self {
         self.n_term = term;
         self
     }
 
-    /// Add the C terminal modification
+    /// Set the C terminal modifications
     #[must_use]
-    pub fn c_term(mut self, term: Option<Modification>) -> Self {
+    pub fn c_term(mut self, term: Vec<Modification>) -> Self {
         self.c_term = term;
         self
     }
 
+    /// Set the N terminal modifications
+    pub fn set_n_term(&mut self, term: Vec<Modification>) {
+        self.n_term = term;
+    }
+
+    /// Set the C terminal modifications
+    pub fn set_c_term(&mut self, term: Vec<Modification>) {
+        self.c_term = term;
+    }
+
     /// Get the number of amino acids making up this peptide
     pub fn len(&self) -> usize {
         self.sequence.len()
@@ -347,24 +370,24 @@ impl<Complexity> LinearPeptide<Complexity> {
         self.sequence.is_empty()
     }
 
-    /// Get the N terminal modification.
-    pub const fn get_n_term(&self) -> Option<&Modification> {
-        self.n_term.as_ref()
+    /// Get the N terminal modifications.
+    pub fn get_n_term(&self) -> &[Modification] {
+        &self.n_term
     }
 
-    /// Get the C terminal modification.
-    pub const fn get_c_term(&self) -> Option<&Modification> {
-        self.c_term.as_ref()
+    /// Get the C terminal modifications.
+    pub fn get_c_term(&self) -> &[Modification] {
+        &self.c_term
     }
 
     /// Set the N terminal modification as a simple modification
-    pub fn set_simple_n_term(&mut self, modification: Option<SimpleModification>) {
-        self.n_term = modification.map(Modification::Simple);
+    pub fn add_simple_n_term(&mut self, modification: SimpleModification) {
+        self.n_term.push(Modification::Simple(modification));
     }
 
     /// Set the C terminal modification as a simple modification
-    pub fn set_simple_c_term(&mut self, modification: Option<SimpleModification>) {
-        self.c_term = modification.map(Modification::Simple);
+    pub fn add_simple_c_term(&mut self, modification: SimpleModification) {
+        self.c_term.push(Modification::Simple(modification));
     }
 
     /// Add a modification to this peptide
@@ -374,8 +397,8 @@ impl<Complexity> LinearPeptide<Complexity> {
         modification: SimpleModification,
     ) {
         match position {
-            SequencePosition::NTerm => self.set_simple_n_term(Some(modification)),
-            SequencePosition::CTerm => self.set_simple_c_term(Some(modification)),
+            SequencePosition::NTerm => self.add_simple_n_term(modification),
+            SequencePosition::CTerm => self.add_simple_c_term(modification),
             SequencePosition::Index(index) => self.sequence[index]
                 .modifications
                 .push(Modification::Simple(modification)),
@@ -390,44 +413,54 @@ impl<Complexity> LinearPeptide<Complexity> {
     /// The mass of the N terminal modifications. The global isotope modifications are NOT applied.
     fn get_n_term_mass(
         &self,
-        all_peptides: &[LinearPeptide<Linked>],
+        all_peptides: &[Peptidoform<Linked>],
         visited_peptides: &[usize],
         applied_cross_links: &mut Vec<CrossLinkName>,
         allow_ms_cleavable: bool,
-        peptide_index: usize,
+        peptidoform_index: usize,
     ) -> Multi<MolecularFormula> {
-        self.n_term.as_ref().map_or_else(Multi::default, |f| {
-            f.formula_inner(
-                all_peptides,
-                visited_peptides,
-                applied_cross_links,
-                allow_ms_cleavable,
-                SequencePosition::NTerm,
-                peptide_index,
-            )
-            .0
+        self.n_term.iter().fold(Multi::default(), |acc, f| {
+            if let Modification::Ambiguous { .. } = f {
+                acc
+            } else {
+                acc * f
+                    .formula_inner(
+                        all_peptides,
+                        visited_peptides,
+                        applied_cross_links,
+                        allow_ms_cleavable,
+                        SequencePosition::NTerm,
+                        peptidoform_index,
+                    )
+                    .0
+            }
         }) + molecular_formula!(H 1)
     }
 
     /// The mass of the C terminal modifications. The global isotope modifications are NOT applied.
     fn get_c_term_mass(
         &self,
-        all_peptides: &[LinearPeptide<Linked>],
+        all_peptides: &[Peptidoform<Linked>],
         visited_peptides: &[usize],
         applied_cross_links: &mut Vec<CrossLinkName>,
         allow_ms_cleavable: bool,
-        peptide_index: usize,
+        peptidoform_index: usize,
     ) -> Multi<MolecularFormula> {
-        self.c_term.as_ref().map_or_else(Multi::default, |f| {
-            f.formula_inner(
-                all_peptides,
-                visited_peptides,
-                applied_cross_links,
-                allow_ms_cleavable,
-                SequencePosition::CTerm,
-                peptide_index,
-            )
-            .0
+        self.c_term.iter().fold(Multi::default(), |acc, f| {
+            if let Modification::Ambiguous { .. } = f {
+                acc
+            } else {
+                acc * f
+                    .formula_inner(
+                        all_peptides,
+                        visited_peptides,
+                        applied_cross_links,
+                        allow_ms_cleavable,
+                        SequencePosition::CTerm,
+                        peptidoform_index,
+                    )
+                    .0
+            }
         }) + molecular_formula!(H 1 O 1)
     }
 
@@ -435,11 +468,11 @@ impl<Complexity> LinearPeptide<Complexity> {
     fn potential_neutral_losses(
         &self,
         range: impl RangeBounds<usize>,
-        all_peptides: &[LinearPeptide<Linked>],
-        peptide_index: usize,
+        all_peptides: &[Peptidoform<Linked>],
+        peptidoform_index: usize,
         ignore_peptides: &mut Vec<usize>,
     ) -> Vec<(NeutralLoss, usize, SequencePosition)> {
-        ignore_peptides.push(peptide_index);
+        ignore_peptides.push(peptidoform_index);
         let mut found_peptides = Vec::new();
         let own_losses = self
             .iter(range)
@@ -465,7 +498,7 @@ impl<Complexity> LinearPeptide<Complexity> {
                                     })
                                     .flatten()
                                     .map(move |loss| {
-                                        (loss.clone(), peptide_index, pos.sequence_index)
+                                        (loss.clone(), peptidoform_index, pos.sequence_index)
                                     })
                                     .collect_vec(),
                             ),
@@ -484,7 +517,7 @@ impl<Complexity> LinearPeptide<Complexity> {
                             Some(
                                 neutral
                                     .into_iter()
-                                    .map(|n| (n, peptide_index, pos.sequence_index))
+                                    .map(|n| (n, peptidoform_index, pos.sequence_index))
                                     .collect_vec(),
                             )
                         }
@@ -581,18 +614,18 @@ impl<Complexity> LinearPeptide<Complexity> {
     /// It always contains at least one pattern.
     /// The global isotope modifications are NOT applied.
     /// Additionally it also returns all peptides present as cross-link.
-    // TODO: take terminal ambiguous into account
-    #[allow(clippy::too_many_arguments)]
+    // TODO: support limit and colocalise
+    #[expect(clippy::too_many_arguments)]
     fn ambiguous_patterns(
         &self,
         range: impl RangeBounds<usize>,
         aa_range: impl RangeBounds<usize> + Clone,
         base: &Multi<MolecularFormula>,
-        all_peptides: &[LinearPeptide<Linked>],
+        all_peptides: &[Peptidoform<Linked>],
         visited_peptides: &[usize],
         applied_cross_links: &mut Vec<CrossLinkName>,
         allow_ms_cleavable: bool,
-        peptide_index: usize,
+        peptidoform_index: usize,
     ) -> (Multi<MolecularFormula>, HashSet<CrossLinkName>) {
         // Calculate all formulas for the selected AA range without any ambiguous modifications
         let (formulas, seen) = self.sequence[(
@@ -610,7 +643,7 @@ impl<Complexity> LinearPeptide<Complexity> {
                         applied_cross_links,
                         allow_ms_cleavable,
                         SequencePosition::Index(index),
-                        peptide_index,
+                        peptidoform_index,
                     );
                     (
                         previous_aa_formulas.0 * f,
@@ -620,77 +653,86 @@ impl<Complexity> LinearPeptide<Complexity> {
             );
 
         // Calculate all masses (and labels) for all possible combinations of ambiguous masses
-        let previous_combinations = self.ambiguous_modifications.iter().enumerate().fold(
-            vec![Vec::new()],
-            |previous_combinations, (id, possibilities)| {
+        let previous_combinations = self
+            .modifications_of_unknown_position
+            .iter()
+            .enumerate()
+            .fold(vec![Vec::new()], |previous_combinations, (id, entry)| {
                 // Go over all possible locations for this ambiguous mod and add these to all previous options
-                let new_combinations = possibilities
+                let in_range_positions = entry
+                    .positions
                     .iter()
                     .filter(|pos| peptide_range_contains(&range, self.len(), **pos))
-                    .flat_map(|pos| {
-                        // This position is a possible location, add this location for this mod to all previously known combinations
-                        let mut new_combinations = previous_combinations
-                            .iter()
-                            .map(|path| {
-                                let mut new = path.clone();
-                                new.push(Some((id, *pos)));
-                                new
-                            })
-                            .collect_vec();
-                        // If there is an option to place this mod outside of this range allow that as well
-                        // by copying all previous options without any alteration
-                        if possibilities
-                            .iter()
-                            .any(|pos| !peptide_range_contains(&range, self.len(), *pos))
-                        {
-                            new_combinations.extend_from_slice(&previous_combinations);
-                        }
-                        new_combinations
-                    })
                     .collect_vec();
 
-                // If no location is possible for this modification keep all known combinations
-                if new_combinations.is_empty() {
+                if in_range_positions.is_empty() {
+                    // If no location is possible for this modification keep all known combinations
                     previous_combinations
                 } else {
-                    new_combinations
+                    // Returns a list of all combinations of ambiguous modifications that can go together
+                    let mut options = in_range_positions
+                        .iter()
+                        .flat_map(|pos| {
+                            // This position is a possible location, add this location for this mod to all previously known combinations
+                            previous_combinations
+                                .iter()
+                                .filter(|path| {
+                                    entry.colocalise_modifications_of_unknown_position
+                                        || path.iter().all(|(_, l)| l != pos)
+                                })
+                                .map(|path| {
+                                    let mut new = path.clone();
+                                    new.push((id, *pos));
+                                    new
+                                })
+                                .collect_vec()
+                        })
+                        .collect_vec();
+                    // If there is an option to place this mod outside of this range allow that as well
+                    // by copying all previous options without any alteration
+                    if in_range_positions.len() < entry.positions.len() {
+                        options.extend_from_slice(&previous_combinations);
+                    }
+                    options
                 }
-                // Returns a list of all combinations of ambiguous modifications that can go together
-            },
-        );
+            });
+
+        // Determine the formula for all selected ambiguous modifications and create the labels
         let all_ambiguous_options = previous_combinations
             .into_iter()
             .map(|current_selected_ambiguous| {
-                // Determine the formula for all selected ambiguous modifications and create the labels
                 current_selected_ambiguous
                     .iter()
                     .copied()
-                    .filter_map(|position| {
-                        if let Some((id, pos)) = position {
-                            self[pos].modifications.iter().find_map(|m| {
-                                // TODO: incorrect N/C handling
-                                if let Modification::Ambiguous {
-                                    id: mid,
-                                    modification,
-                                    ..
-                                } = m
-                                {
-                                    (*mid == id).then(|| {
-                                        modification.formula_inner(pos, peptide_index).with_label(
-                                            AmbiguousLabel::Modification {
-                                                id,
-                                                sequence_index: pos,
-                                                peptide_index,
-                                            },
-                                        )
-                                    })
-                                } else {
-                                    None
-                                }
-                            })
-                        } else {
-                            Some(MolecularFormula::default())
+                    .filter_map(|(id, pos)| {
+                        match pos {
+                            SequencePosition::NTerm => self.n_term.as_slice(),
+                            SequencePosition::Index(i) => {
+                                self.sequence[*i].modifications.as_slice()
+                            }
+                            SequencePosition::CTerm => self.c_term.as_slice(),
                         }
+                        .iter()
+                        .find_map(|m| {
+                            if let Modification::Ambiguous {
+                                id: mid,
+                                modification,
+                                ..
+                            } = m
+                            {
+                                (*mid == id).then(|| {
+                                    modification
+                                        .formula_inner(*pos, peptidoform_index)
+                                        .with_label(AmbiguousLabel::Modification {
+                                            id,
+                                            sequence_index: *pos,
+                                            peptidoform_index,
+                                        })
+                                })
+                            } else {
+                                None
+                            }
+                        })
                     })
                     .sum::<MolecularFormula>()
             })
@@ -706,9 +748,9 @@ impl<Complexity> LinearPeptide<Complexity> {
         &self,
         max_charge: Charge,
         model: &Model,
+        peptidoform_ion_index: usize,
         peptidoform_index: usize,
-        peptide_index: usize,
-        all_peptides: &[LinearPeptide<Linked>],
+        all_peptides: &[Peptidoform<Linked>],
     ) -> Vec<Fragment> {
         let default_charge = MolecularCharge::proton(
             isize::try_from(max_charge.value)
@@ -724,7 +766,7 @@ impl<Complexity> LinearPeptide<Complexity> {
         for sequence_index in 0..self.sequence.len() {
             let position = PeptidePosition::n(SequencePosition::Index(sequence_index), self.len());
             let mut cross_links = Vec::new();
-            let visited_peptides = vec![peptide_index];
+            let visited_peptides = vec![peptidoform_index];
             let (n_term, n_term_seen) = self.all_masses(
                 ..=sequence_index,
                 ..sequence_index,
@@ -733,14 +775,14 @@ impl<Complexity> LinearPeptide<Complexity> {
                     &visited_peptides,
                     &mut cross_links,
                     model.allow_cross_link_cleavage,
-                    peptide_index,
+                    peptidoform_index,
                 ),
                 model.modification_specific_neutral_losses,
                 all_peptides,
                 &visited_peptides,
                 &mut cross_links,
                 model.allow_cross_link_cleavage,
-                peptide_index,
+                peptidoform_index,
             );
             let (c_term, c_term_seen) = self.all_masses(
                 sequence_index..,
@@ -750,14 +792,14 @@ impl<Complexity> LinearPeptide<Complexity> {
                     &visited_peptides,
                     &mut cross_links,
                     model.allow_cross_link_cleavage,
-                    peptide_index,
+                    peptidoform_index,
                 ),
                 model.modification_specific_neutral_losses,
                 all_peptides,
                 &visited_peptides,
                 &mut cross_links,
                 model.allow_cross_link_cleavage,
-                peptide_index,
+                peptidoform_index,
             );
             if !n_term_seen.is_disjoint(&c_term_seen) {
                 continue; // There is a link reachable from both sides so there is a loop
@@ -768,11 +810,11 @@ impl<Complexity> LinearPeptide<Complexity> {
                 .fold((Multi::default(), HashSet::new()), |acc, m| {
                     let (f, s) = m.formula_inner(
                         all_peptides,
-                        &[peptide_index],
+                        &[peptidoform_index],
                         &mut cross_links,
                         model.allow_cross_link_cleavage,
                         SequencePosition::Index(sequence_index),
-                        peptide_index,
+                        peptidoform_index,
                     );
                     (acc.0 * f, acc.1.union(&s).cloned().collect())
                 });
@@ -789,8 +831,8 @@ impl<Complexity> LinearPeptide<Complexity> {
                         SequencePosition::Index(sequence_index),
                         self.sequence.len(),
                         &model.ions(position),
+                        peptidoform_ion_index,
                         peptidoform_index,
-                        peptide_index,
                         (
                             // Allow any N terminal fragment if there is no cross-link to the C terminal side
                             c_term_seen.is_disjoint(&modifications_cross_links),
@@ -803,7 +845,7 @@ impl<Complexity> LinearPeptide<Complexity> {
                 //  p - sX fragment: precursor amino acid side chain losses
                 output.extend(
                     self.formulas_inner(
-                        peptide_index,
+                        peptidoform_index,
                         all_peptides,
                         &[],
                         &mut Vec::new(),
@@ -814,14 +856,17 @@ impl<Complexity> LinearPeptide<Complexity> {
                     .flat_map(|m| {
                         self.sequence[sequence_index]
                             .aminoacid
-                            .formulas_inner(SequencePosition::Index(sequence_index), peptide_index)
+                            .formulas_inner(
+                                SequencePosition::Index(sequence_index),
+                                peptidoform_index,
+                            )
                             .iter()
                             .flat_map(|aa| {
                                 Fragment::generate_all(
                                     &((-modifications_total.clone()) + m.clone() - aa.clone()
                                         + molecular_formula!(C 2 H 2 N 1 O 1)),
+                                    peptidoform_ion_index,
                                     peptidoform_index,
-                                    peptide_index,
                                     &FragmentType::PrecursorSideChainLoss(
                                         position,
                                         self.sequence[sequence_index].aminoacid.aminoacid(),
@@ -846,7 +891,7 @@ impl<Complexity> LinearPeptide<Complexity> {
 
         // Generate precursor peak
         let (full_precursor, _all_cross_links) = self.formulas_inner(
-            peptide_index,
+            peptidoform_index,
             all_peptides,
             &[],
             &mut Vec::new(),
@@ -854,7 +899,7 @@ impl<Complexity> LinearPeptide<Complexity> {
         );
         // Allow neutral losses from modifications for the precursor
         let mut precursor_neutral_losses = if model.modification_specific_neutral_losses {
-            self.potential_neutral_losses(.., all_peptides, peptide_index, &mut Vec::new())
+            self.potential_neutral_losses(.., all_peptides, peptidoform_index, &mut Vec::new())
                 .into_iter()
                 .map(|(n, _, _)| n)
                 .collect_vec()
@@ -865,8 +910,8 @@ impl<Complexity> LinearPeptide<Complexity> {
 
         output.extend(Fragment::generate_all(
             &full_precursor,
+            peptidoform_ion_index,
             peptidoform_index,
-            peptide_index,
             &FragmentType::Precursor,
             &Multi::default(),
             &precursor_neutral_losses,
@@ -879,7 +924,7 @@ impl<Complexity> LinearPeptide<Complexity> {
         // and that no peptide fragmentation occurs during glycan fragmentation
         let full_formula = self
             .formulas_inner(
-                peptide_index,
+                peptidoform_index,
                 all_peptides,
                 &[],
                 &mut Vec::new(),
@@ -891,8 +936,8 @@ impl<Complexity> LinearPeptide<Complexity> {
             for modification in &position.modifications {
                 output.extend(modification.generate_theoretical_fragments(
                     model,
+                    peptidoform_ion_index,
                     peptidoform_index,
-                    peptide_index,
                     &mut charge_carriers,
                     &full_formula,
                     Some(attachment),
@@ -908,8 +953,8 @@ impl<Complexity> LinearPeptide<Complexity> {
                         formula: Some(dia.0),
                         charge: Charge::default(),
                         ion: FragmentType::Diagnostic(pos),
+                        peptidoform_ion_index: Some(peptidoform_ion_index),
                         peptidoform_index: Some(peptidoform_index),
-                        peptide_index: Some(peptide_index),
                         neutral_loss: Vec::new(),
                         deviation: None,
                         confidence: None,
@@ -930,8 +975,8 @@ impl<Complexity> LinearPeptide<Complexity> {
                     output.extend(MonoSaccharide::theoretical_fragments(
                         composition,
                         model,
+                        peptidoform_ion_index,
                         peptidoform_index,
-                        peptide_index,
                         &mut charge_carriers,
                         &full_formula,
                         None,
@@ -948,8 +993,8 @@ impl<Complexity> LinearPeptide<Complexity> {
                             .determine_positions()
                             .generate_theoretical_fragments(
                                 model,
+                                peptidoform_ion_index,
                                 peptidoform_index,
-                                peptide_index,
                                 &mut charge_carriers,
                                 &full_formula,
                                 None,
@@ -966,18 +1011,18 @@ impl<Complexity> LinearPeptide<Complexity> {
     /// Generate all potential masses for the given stretch of amino acids alongside all peptides seen as part of a cross-link.
     /// Applies ambiguous amino acids and modifications, and neutral losses (if allowed in the model).
     // TODO: take terminal ambiguous into account
-    #[allow(clippy::too_many_arguments)]
+    #[expect(clippy::too_many_arguments)]
     fn all_masses(
         &self,
         range: impl RangeBounds<usize> + Clone,
         aa_range: impl RangeBounds<usize> + Clone,
         base: &Multi<MolecularFormula>,
         apply_neutral_losses: bool,
-        all_peptides: &[LinearPeptide<Linked>],
+        all_peptides: &[Peptidoform<Linked>],
         visited_peptides: &[usize],
         applied_cross_links: &mut Vec<CrossLinkName>,
         allow_ms_cleavable: bool,
-        peptide_index: usize,
+        peptidoform_index: usize,
     ) -> (Multi<MolecularFormula>, HashSet<CrossLinkName>) {
         let (ambiguous_mods_masses, seen) = self.ambiguous_patterns(
             range.clone(),
@@ -987,11 +1032,15 @@ impl<Complexity> LinearPeptide<Complexity> {
             visited_peptides,
             applied_cross_links,
             allow_ms_cleavable,
-            peptide_index,
+            peptidoform_index,
         );
         if apply_neutral_losses {
-            let neutral_losses =
-                self.potential_neutral_losses(range, all_peptides, peptide_index, &mut Vec::new());
+            let neutral_losses = self.potential_neutral_losses(
+                range,
+                all_peptides,
+                peptidoform_index,
+                &mut Vec::new(),
+            );
             let mut all_masses =
                 Vec::with_capacity(ambiguous_mods_masses.len() * (1 + neutral_losses.len()));
             all_masses.extend(ambiguous_mods_masses.iter().cloned());
@@ -1006,21 +1055,21 @@ impl<Complexity> LinearPeptide<Complexity> {
 
     /// Get the total amount of ambiguous modifications
     pub(crate) fn number_of_ambiguous_modifications(&self) -> usize {
-        self.ambiguous_modifications.len()
+        self.modifications_of_unknown_position.len()
     }
 
     /// Gives all the formulas for the whole peptide with no C and N terminal modifications. With the global isotope modifications applied.
-    #[allow(clippy::missing_panics_doc)] // Global isotope mods are guaranteed to be correct
+    #[expect(clippy::missing_panics_doc)] // Global isotope mods are guaranteed to be correct
     fn bare_formulas_inner(
         &self,
-        all_peptides: &[LinearPeptide<Linked>],
+        all_peptides: &[Peptidoform<Linked>],
         visited_peptides: &[usize],
         applied_cross_links: &mut Vec<CrossLinkName>,
         allow_ms_cleavable: bool,
-        peptide_index: usize,
+        peptidoform_index: usize,
     ) -> Multi<MolecularFormula> {
         let mut formulas = Multi::default();
-        let mut placed = vec![false; self.ambiguous_modifications.len()];
+        let mut placed = vec![false; self.modifications_of_unknown_position.len()];
         for (index, pos) in self.sequence.iter().enumerate() {
             formulas *= pos
                 .formulas_greedy(
@@ -1030,7 +1079,7 @@ impl<Complexity> LinearPeptide<Complexity> {
                     applied_cross_links,
                     allow_ms_cleavable,
                     SequencePosition::Index(index),
-                    peptide_index,
+                    peptidoform_index,
                 )
                 .0;
         }
@@ -1049,32 +1098,32 @@ impl<Complexity> LinearPeptide<Complexity> {
     /// When this peptide is already in the set of visited peptides.
     pub(crate) fn formulas_inner(
         &self,
-        peptide_index: usize,
-        all_peptides: &[LinearPeptide<Linked>],
+        peptidoform_index: usize,
+        all_peptides: &[Peptidoform<Linked>],
         visited_peptides: &[usize],
         applied_cross_links: &mut Vec<CrossLinkName>,
         allow_ms_cleavable: bool,
     ) -> (Multi<MolecularFormula>, HashSet<CrossLinkName>) {
         debug_assert!(
-            !visited_peptides.contains(&peptide_index),
+            !visited_peptides.contains(&peptidoform_index),
             "Cannot get the formula for a peptide that is already visited"
         );
-        let mut new_visited_peptides = vec![peptide_index];
+        let mut new_visited_peptides = vec![peptidoform_index];
         new_visited_peptides.extend_from_slice(visited_peptides);
         let mut formulas: Multi<MolecularFormula> = self.get_n_term_mass(
             all_peptides,
             visited_peptides,
             applied_cross_links,
             allow_ms_cleavable,
-            peptide_index,
+            peptidoform_index,
         ) * self.get_c_term_mass(
             all_peptides,
             visited_peptides,
             applied_cross_links,
             allow_ms_cleavable,
-            peptide_index,
+            peptidoform_index,
         );
-        let mut placed = vec![false; self.ambiguous_modifications.len()];
+        let mut placed = vec![false; self.modifications_of_unknown_position.len()];
         let mut seen = HashSet::new();
         for (index, pos) in self.sequence.iter().enumerate() {
             let (pos_f, pos_seen) = pos.formulas_greedy(
@@ -1084,7 +1133,7 @@ impl<Complexity> LinearPeptide<Complexity> {
                 applied_cross_links,
                 allow_ms_cleavable,
                 SequencePosition::Index(index),
-                peptide_index,
+                peptidoform_index,
             );
             formulas *= pos_f;
             seen.extend(pos_seen);
@@ -1125,13 +1174,21 @@ impl<Complexity> LinearPeptide<Complexity> {
         // Write any modification of unknown position that has no preferred location at the start of the peptide
         let mut any_ambiguous = false;
         let mut placed_ambiguous = Vec::new();
-        let mut preferred_ambiguous_position = vec![None; self.ambiguous_modifications.len()];
-        for (id, ambiguous) in self.ambiguous_modifications.iter().enumerate() {
+        let mut preferred_ambiguous_position =
+            vec![None; self.modifications_of_unknown_position.len()];
+        for (id, ambiguous) in self.modifications_of_unknown_position.iter().enumerate() {
             if let Some(preferred) = ambiguous
+                .positions
                 .iter()
                 .find_map(|i| {
                     let m = match i {
-                        SequencePosition::NTerm => self.n_term.as_ref(),
+                        SequencePosition::NTerm => self.n_term.iter().find(|m| {
+                            if let Modification::Ambiguous { id: mid, .. } = m {
+                                *mid == id
+                            } else {
+                                false
+                            }
+                        }),
                         SequencePosition::Index(i) => {
                             self.sequence[*i].modifications.iter().find(|m| {
                                 if let Modification::Ambiguous { id: mid, .. } = m {
@@ -1141,7 +1198,13 @@ impl<Complexity> LinearPeptide<Complexity> {
                                 }
                             })
                         }
-                        SequencePosition::CTerm => self.c_term.as_ref(),
+                        SequencePosition::CTerm => self.c_term.iter().find(|m| {
+                            if let Modification::Ambiguous { id: mid, .. } = m {
+                                *mid == id
+                            } else {
+                                false
+                            }
+                        }),
                     };
 
                     if let Some(Modification::Ambiguous {
@@ -1153,12 +1216,18 @@ impl<Complexity> LinearPeptide<Complexity> {
                         None
                     }
                 })
-                .or_else(|| (ambiguous.len() == 1).then_some(ambiguous[0]))
+                .or_else(|| (ambiguous.positions.len() == 1).then_some(ambiguous.positions[0]))
             {
                 preferred_ambiguous_position[id] = Some(preferred);
             } else {
-                let m = match ambiguous.first() {
-                    Some(SequencePosition::NTerm) => self.n_term.as_ref(),
+                let m = match ambiguous.positions.first() {
+                    Some(SequencePosition::NTerm) => self.n_term.iter().find(|m| {
+                        if let Modification::Ambiguous { id: mid, .. } = m {
+                            *mid == id
+                        } else {
+                            false
+                        }
+                    }),
                     Some(SequencePosition::Index(i)) => {
                         self.sequence[*i].modifications.iter().find(|m| {
                             if let Modification::Ambiguous { id: mid, .. } = m {
@@ -1168,7 +1237,13 @@ impl<Complexity> LinearPeptide<Complexity> {
                             }
                         })
                     }
-                    Some(SequencePosition::CTerm) => self.c_term.as_ref(),
+                    Some(SequencePosition::CTerm) => self.c_term.iter().find(|m| {
+                        if let Modification::Ambiguous { id: mid, .. } = m {
+                            *mid == id
+                        } else {
+                            false
+                        }
+                    }),
                     None => None,
                 };
                 if let Some(m) = m {
@@ -1183,10 +1258,11 @@ impl<Complexity> LinearPeptide<Complexity> {
         if any_ambiguous {
             write!(f, "?")?;
         }
-        if let Some(m) = &self.n_term {
+        let mut any_n = false;
+        for m in self.get_n_term() {
             let mut display_ambiguous = false;
 
-            if let Some(Modification::Ambiguous { id, .. }) = self.get_n_term() {
+            if let Modification::Ambiguous { id, .. } = m {
                 if !placed_ambiguous.contains(id) && preferred_ambiguous_position[*id].is_none()
                     || preferred_ambiguous_position[*id]
                         .is_some_and(|p| p == SequencePosition::NTerm)
@@ -1198,7 +1274,11 @@ impl<Complexity> LinearPeptide<Complexity> {
 
             write!(f, "[")?;
             m.display(f, specification_compliant, display_ambiguous)?;
-            write!(f, "]-")?;
+            write!(f, "]")?;
+            any_n = true;
+        }
+        if any_n {
+            write!(f, "-")?;
         }
         let mut last_ambiguous = None;
         for (index, position) in self.sequence.iter().enumerate() {
@@ -1215,13 +1295,18 @@ impl<Complexity> LinearPeptide<Complexity> {
         if last_ambiguous.is_some() {
             write!(f, ")")?;
         }
-        if let Some(m) = &self.c_term {
+        let mut first = true;
+        for m in self.get_c_term() {
             let mut display_ambiguous = false;
             if let Modification::Ambiguous { id, .. } = m {
                 display_ambiguous = !placed_ambiguous.contains(id);
                 placed_ambiguous.push(*id);
             }
-            write!(f, "-[")?;
+            if first {
+                write!(f, "-")?;
+                first = false;
+            }
+            write!(f, "[")?;
             m.display(f, specification_compliant, display_ambiguous)?;
             write!(f, "]")?;
         }
@@ -1238,11 +1323,18 @@ impl<Complexity> LinearPeptide<Complexity> {
             n_term: self.c_term.clone(),
             c_term: self.n_term.clone(),
             sequence: self.sequence.clone().into_iter().rev().collect(),
-            ambiguous_modifications: self
-                .ambiguous_modifications
+            modifications_of_unknown_position: self
+                .modifications_of_unknown_position
                 .clone()
                 .into_iter()
-                .map(|m| m.into_iter().map(|loc| loc.reverse(self.len())).collect())
+                .map(|m| AmbiguousEntry {
+                    positions: m
+                        .positions
+                        .into_iter()
+                        .map(|loc| loc.reverse(self.len()))
+                        .collect(),
+                    ..m
+                })
                 .collect(),
             ..self.clone()
         }
@@ -1253,7 +1345,7 @@ impl<Complexity> LinearPeptide<Complexity> {
     }
 }
 
-impl LinearPeptide<Linked> {
+impl Peptidoform<Linked> {
     /// Add a modification to this peptide
     pub(crate) fn add_modification(
         &mut self,
@@ -1261,24 +1353,24 @@ impl LinearPeptide<Linked> {
         modification: Modification,
     ) {
         match position {
-            SequencePosition::NTerm => self.n_term = Some(modification),
-            SequencePosition::CTerm => self.c_term = Some(modification),
+            SequencePosition::NTerm => self.n_term.push(modification),
+            SequencePosition::CTerm => self.c_term.push(modification),
             SequencePosition::Index(index) => self.sequence[index].modifications.push(modification),
         }
     }
 
     /// Set the N terminal modification
-    pub fn set_n_term(&mut self, modification: Option<Modification>) {
-        self.n_term = modification;
+    pub fn add_n_term(&mut self, modification: Modification) {
+        self.n_term.push(modification);
     }
 
     /// Set the C terminal modification
-    pub fn set_c_term(&mut self, modification: Option<Modification>) {
-        self.c_term = modification;
+    pub fn add_c_term(&mut self, modification: Modification) {
+        self.c_term.push(modification);
     }
 }
 
-impl LinearPeptide<Linear> {
+impl Peptidoform<Linear> {
     /// Add the charge carriers.
     #[must_use]
     pub fn charge_carriers(mut self, charge: Option<MolecularCharge>) -> Self {
@@ -1287,7 +1379,7 @@ impl LinearPeptide<Linear> {
     }
 }
 
-impl<Complexity: AtMax<Linear>> LinearPeptide<Complexity> {
+impl<Complexity: AtMax<Linear>> Peptidoform<Complexity> {
     /// Get a region of this peptide as a new peptide (with all terminal/global/ambiguous modifications).
     #[must_use]
     pub fn sub_peptide(&self, index: impl RangeBounds<usize>) -> Self {
@@ -1295,12 +1387,12 @@ impl<Complexity: AtMax<Linear>> LinearPeptide<Complexity> {
             n_term: if index.contains(&0) {
                 self.n_term.clone()
             } else {
-                None
+                Vec::new()
             },
             c_term: if index.contains(&(self.len() - 1)) {
                 self.c_term.clone()
             } else {
-                None
+                Vec::new()
             },
             sequence: self.sequence[(index.start_bound().cloned(), index.end_bound().cloned())]
                 .to_vec(),
@@ -1324,22 +1416,20 @@ impl<Complexity: AtMax<Linear>> LinearPeptide<Complexity> {
         result
     }
 
-    /// Get the N terminal modification as a simple modification
-    pub fn get_simple_n_term(&self) -> Option<&SimpleModification> {
-        match &self.n_term {
-            Some(Modification::Simple(simple)) => Some(simple),
-            Some(_) => unreachable!(),
-            _ => None,
-        }
+    /// Get the N terminal modifications as simple modifications
+    pub fn get_simple_n_term(&self) -> Vec<SimpleModification> {
+        self.n_term
+            .iter()
+            .filter_map(|m| m.clone().into_simple())
+            .collect()
     }
 
-    /// Get the C terminal modification as a simple modification
-    pub fn get_simple_c_term(&self) -> Option<&SimpleModification> {
-        match &self.c_term {
-            Some(Modification::Simple(simple)) => Some(simple),
-            Some(_) => unreachable!(),
-            _ => None,
-        }
+    /// Get the C terminal modifications as simple modifications
+    pub fn get_simple_c_term(&self) -> Vec<SimpleModification> {
+        self.c_term
+            .iter()
+            .filter_map(|m| m.clone().into_simple())
+            .collect()
     }
 
     /// Generate the theoretical fragments for this peptide, with the given maximal charge of the fragments, and the given model.
@@ -1356,12 +1446,12 @@ impl<Complexity: AtMax<Linear>> LinearPeptide<Complexity> {
     }
 
     /// Gives the formulas for the whole peptide. With the global isotope modifications applied. (Any B/Z will result in multiple possible formulas.)
-    #[allow(clippy::missing_panics_doc)] // Can not panic (unless state is already corrupted)
+    #[expect(clippy::missing_panics_doc)] // Can not panic (unless state is already corrupted)
     pub fn formulas(&self) -> Multi<MolecularFormula> {
         let mut formulas: Multi<MolecularFormula> =
             self.get_n_term_mass(&[], &[], &mut Vec::new(), false, 0)
                 * self.get_c_term_mass(&[], &[], &mut Vec::new(), false, 0);
-        let mut placed = vec![false; self.ambiguous_modifications.len()];
+        let mut placed = vec![false; self.modifications_of_unknown_position.len()];
         for (index, pos) in self.sequence.iter().enumerate() {
             formulas *= pos
                 .formulas_greedy(
@@ -1388,9 +1478,9 @@ impl<Complexity: AtMax<Linear>> LinearPeptide<Complexity> {
     }
 }
 
-impl LinearPeptide<UnAmbiguous> {
+impl Peptidoform<UnAmbiguous> {
     /// Gives the formula for the whole peptide. With the global isotope modifications applied.
-    #[allow(clippy::missing_panics_doc)] // Can not panic (unless state is already corrupted)
+    #[expect(clippy::missing_panics_doc)] // Can not panic (unless state is already corrupted)
     pub fn formula(&self) -> MolecularFormula {
         let mut options = self
             .formulas_inner(0, &[], &[], &mut Vec::new(), false)
@@ -1401,7 +1491,7 @@ impl LinearPeptide<UnAmbiguous> {
     }
 
     /// Gives the formula for the whole peptide with no C and N terminal modifications. With the global isotope modifications applied.
-    #[allow(clippy::missing_panics_doc)] // Can not panic (unless state is already corrupted)
+    #[expect(clippy::missing_panics_doc)] // Can not panic (unless state is already corrupted)
     pub fn bare_formula(&self) -> MolecularFormula {
         let mut options = self
             .bare_formulas_inner(&[], &[], &mut Vec::new(), false, 0)
@@ -1411,7 +1501,7 @@ impl LinearPeptide<UnAmbiguous> {
     }
 }
 
-impl<Complexity: AtLeast<Linear>> LinearPeptide<Complexity> {
+impl<Complexity: AtLeast<Linear>> Peptidoform<Complexity> {
     /// Get the global isotope modifications
     pub fn get_global(&self) -> &[(Element, Option<NonZeroU16>)] {
         &self.global
@@ -1454,12 +1544,57 @@ impl<Complexity: AtLeast<Linear>> LinearPeptide<Complexity> {
     }
 }
 
-impl<Complexity: AtLeast<SimpleLinear>> LinearPeptide<Complexity> {
+impl<Complexity: AtLeast<SimpleLinear>> Peptidoform<Complexity> {
     /// Get the locations of all ambiguous modifications. The slice is indexed by ambiguous
     /// modification id and contains all sequence locations where that ambiguous modification is
     /// potentially located.
-    pub fn get_ambiguous_modifications(&self) -> &[Vec<SequencePosition>] {
-        self.ambiguous_modifications.as_ref()
+    pub fn get_ambiguous_modifications(&self) -> Vec<Vec<SequencePosition>> {
+        self.modifications_of_unknown_position
+            .iter()
+            .map(|e| e.positions.clone())
+            .collect()
+    }
+
+    /// Add a new global modification of unknown position. If the modification would be placed on a
+    /// terminal but something is already placed there it is ignored.
+    /// # Errors
+    /// When there are no possible locations return false, the modification is then not applied.
+    #[must_use]
+    pub fn add_unknown_position_modification(
+        &mut self,
+        modification: SimpleModification,
+        range: impl RangeBounds<usize>,
+        settings: &crate::MUPSettings,
+    ) -> bool {
+        let possible_positions = self
+            .iter(range)
+            .filter(|(position, seq)| {
+                modification
+                    .is_possible(seq, position.sequence_index)
+                    .any_possible()
+                    && (settings.position.is_none()
+                        || settings.position.as_ref().is_some_and(|rules| {
+                            rules
+                                .iter()
+                                .any(|rule| rule.is_possible(seq, position.sequence_index))
+                        }))
+                    && (settings.colocalise_placed_modifications
+                        || self[position.sequence_index]
+                            .modifications
+                            .iter()
+                            .all(Modification::is_ambiguous))
+            })
+            .map(|(position, _)| (position.sequence_index, None))
+            .collect_vec();
+
+        self.add_ambiguous_modification(
+            modification,
+            None,
+            &possible_positions,
+            None,
+            settings.limit,
+            settings.colocalise_modifications_of_unknown_position,
+        )
     }
 
     /// Add a new global modification of unknown position. If the modification would be placed on a
@@ -1506,47 +1641,44 @@ impl<Complexity: AtLeast<SimpleLinear>> LinearPeptide<Complexity> {
         group: Option<String>,
         positions: &[(SequencePosition, Option<OrderedFloat<f64>>)],
         preferred_position: Option<SequencePosition>,
+        limit: Option<usize>,
+        colocalise_modifications_of_unknown_position: bool,
     ) -> bool {
         match positions.len() {
             0 => false,
             1 => {
                 match positions[0].0 {
                     SequencePosition::NTerm => {
-                        self.n_term = Some(modification.into());
+                        self.n_term.push(modification.into());
                     }
                     SequencePosition::Index(pos) => {
                         self.sequence[pos].modifications.push(modification.into());
                         self.sequence[pos].modifications.sort_unstable();
                     }
                     SequencePosition::CTerm => {
-                        self.c_term = Some(modification.into());
+                        self.c_term.push(modification.into());
                     }
                 }
                 true
             }
             _ => {
-                let id = self.ambiguous_modifications.len();
+                let id = self.modifications_of_unknown_position.len();
                 let group = group.unwrap_or_else(|| format!("u{id}"));
                 let mut placed = false;
-                self.ambiguous_modifications.push(
-                    positions
+                self.modifications_of_unknown_position.push(AmbiguousEntry {
+                    positions: positions
                         .iter()
-                        .filter_map(|(spos, score)| match spos {
+                        .map(|(spos, score)| match spos {
                             SequencePosition::NTerm => {
-                                let n_filled = self.n_term.is_none();
-                                if n_filled {
-                                    self.n_term = Some(Modification::Ambiguous {
-                                        id,
-                                        group: group.clone(),
-                                        modification: modification.clone(),
-                                        localisation_score: *score,
-                                        preferred: preferred_position.is_some_and(|p| p == *spos),
-                                    });
-                                    placed = true;
-                                    Some(*spos)
-                                } else {
-                                    None
-                                }
+                                self.n_term.push(Modification::Ambiguous {
+                                    id,
+                                    group: group.clone(),
+                                    modification: modification.clone(),
+                                    localisation_score: *score,
+                                    preferred: preferred_position.is_some_and(|p| p == *spos),
+                                });
+                                placed = true;
+                                *spos
                             }
                             SequencePosition::Index(pos) => {
                                 self.sequence[*pos]
@@ -1560,34 +1692,32 @@ impl<Complexity: AtLeast<SimpleLinear>> LinearPeptide<Complexity> {
                                     });
                                 self.sequence[*pos].modifications.sort_unstable();
                                 placed = true;
-                                Some(*spos)
+                                *spos
                             }
                             SequencePosition::CTerm => {
-                                let c_filled = self.c_term.is_none();
-                                if c_filled {
-                                    self.c_term = Some(Modification::Ambiguous {
-                                        id,
-                                        group: group.clone(),
-                                        modification: modification.clone(),
-                                        localisation_score: *score,
-                                        preferred: preferred_position.is_some_and(|p| p == *spos),
-                                    });
-                                    placed = true;
-                                    Some(*spos)
-                                } else {
-                                    None
-                                }
+                                self.c_term.push(Modification::Ambiguous {
+                                    id,
+                                    group: group.clone(),
+                                    modification: modification.clone(),
+                                    localisation_score: *score,
+                                    preferred: preferred_position.is_some_and(|p| p == *spos),
+                                });
+                                placed = true;
+                                *spos
                             }
                         })
                         .collect(),
-                );
+                    limit,
+                    colocalise_modifications_of_unknown_position,
+                    group: None,
+                });
                 placed
             }
         }
     }
 }
 
-impl<OwnComplexity: AtMax<SemiAmbiguous>> LinearPeptide<OwnComplexity> {
+impl<OwnComplexity: AtMax<SemiAmbiguous>> Peptidoform<OwnComplexity> {
     /// Concatenate another peptide after this peptide. This will fail if any of these conditions are true:
     /// * This peptide has a C terminal modification
     /// * The other peptide has an N terminal modification
@@ -1595,13 +1725,13 @@ impl<OwnComplexity: AtMax<SemiAmbiguous>> LinearPeptide<OwnComplexity> {
     // carriers, global or ambiguous modifications.
     pub fn concatenate<OtherComplexity: AtMax<SemiAmbiguous>>(
         self,
-        other: LinearPeptide<OtherComplexity>,
-    ) -> Option<LinearPeptide<OwnComplexity::HighestLevel>>
+        other: Peptidoform<OtherComplexity>,
+    ) -> Option<Peptidoform<OwnComplexity::HighestLevel>>
     where
         OwnComplexity: HighestOf<OtherComplexity>,
     {
-        if self.c_term.is_none() && other.n_term.is_none() {
-            Some(LinearPeptide::<OwnComplexity::HighestLevel> {
+        if self.c_term.is_empty() && other.n_term.is_empty() {
+            Some(Peptidoform::<OwnComplexity::HighestLevel> {
                 global: self.global,
                 labile: self.labile.into_iter().chain(other.labile).collect(),
                 n_term: self.n_term,
@@ -1612,7 +1742,7 @@ impl<OwnComplexity: AtMax<SemiAmbiguous>> LinearPeptide<OwnComplexity> {
                     .map(SequenceElement::mark)
                     .chain(other.sequence.into_iter().map(SequenceElement::mark))
                     .collect(),
-                ambiguous_modifications: Vec::new(),
+                modifications_of_unknown_position: Vec::new(),
                 charge_carriers: self.charge_carriers,
                 marker: PhantomData,
             })
@@ -1622,13 +1752,13 @@ impl<OwnComplexity: AtMax<SemiAmbiguous>> LinearPeptide<OwnComplexity> {
     }
 }
 
-impl<Complexity> Display for LinearPeptide<Complexity> {
+impl<Complexity> Display for Peptidoform<Complexity> {
     fn fmt(&self, f: &mut std::fmt::Formatter<'_>) -> std::fmt::Result {
         self.display(f, true, true)
     }
 }
 
-impl<Collection, Item, Complexity> From<Collection> for LinearPeptide<Complexity>
+impl<Collection, Item, Complexity> From<Collection> for Peptidoform<Complexity>
 where
     Collection: IntoIterator<Item = Item>,
     Item: Into<SequenceElement<Complexity>>,
@@ -1637,17 +1767,17 @@ where
         Self {
             global: Vec::new(),
             labile: Vec::new(),
-            n_term: None,
-            c_term: None,
+            n_term: Vec::new(),
+            c_term: Vec::new(),
             sequence: value.into_iter().map(std::convert::Into::into).collect(),
-            ambiguous_modifications: Vec::new(),
+            modifications_of_unknown_position: Vec::new(),
             charge_carriers: None,
             marker: PhantomData,
         }
     }
 }
 
-impl<Item, Complexity> FromIterator<Item> for LinearPeptide<Complexity>
+impl<Item, Complexity> FromIterator<Item> for Peptidoform<Complexity>
 where
     Item: Into<SequenceElement<Complexity>>,
 {
@@ -1657,7 +1787,7 @@ where
 }
 
 impl<I: SliceIndex<[SequenceElement<Complexity>]>, Complexity> Index<I>
-    for LinearPeptide<Complexity>
+    for Peptidoform<Complexity>
 {
     type Output = I::Output;
 
@@ -1666,7 +1796,7 @@ impl<I: SliceIndex<[SequenceElement<Complexity>]>, Complexity> Index<I>
     }
 }
 
-impl<Complexity> Index<SequencePosition> for LinearPeptide<Complexity> {
+impl<Complexity> Index<SequencePosition> for Peptidoform<Complexity> {
     type Output = SequenceElement<Complexity>;
 
     fn index(&self, index: SequencePosition) -> &Self::Output {
@@ -1678,7 +1808,7 @@ impl<Complexity> Index<SequencePosition> for LinearPeptide<Complexity> {
     }
 }
 
-impl<Complexity> IndexMut<SequencePosition> for LinearPeptide<Complexity> {
+impl<Complexity> IndexMut<SequencePosition> for Peptidoform<Complexity> {
     fn index_mut(&mut self, index: SequencePosition) -> &mut Self::Output {
         match index {
             SequencePosition::NTerm => &mut self.sequence[0],
@@ -1688,11 +1818,11 @@ impl<Complexity> IndexMut<SequencePosition> for LinearPeptide<Complexity> {
     }
 }
 
-/// Make sure that any lower level of peptide can be cast to a higher level
+/// Make sure that any lower level of Peptidoform can be cast to a higher level
 macro_rules! into {
     ($a:tt => $b:ty) => {
-        impl From<LinearPeptide<$a>> for LinearPeptide<$b> {
-            fn from(other: LinearPeptide<$a>) -> Self {
+        impl From<Peptidoform<$a>> for Peptidoform<$b> {
+            fn from(other: Peptidoform<$a>) -> Self {
                 other.mark()
             }
         }
diff --git a/rustyms/src/peptide/peptidoform.rs b/rustyms/src/peptidoform/peptidoform_ion.rs
similarity index 86%
rename from rustyms/src/peptide/peptidoform.rs
rename to rustyms/src/peptidoform/peptidoform_ion.rs
index 6f72d63b..578181a6 100644
--- a/rustyms/src/peptide/peptidoform.rs
+++ b/rustyms/src/peptidoform/peptidoform_ion.rs
@@ -7,22 +7,22 @@ use crate::{
     modification::{
         CrossLinkName, CrossLinkSide, RulePossible, SimpleModification, SimpleModificationInner,
     },
-    peptide::Linked,
+    peptidoform::Linked,
     system::usize::Charge,
-    Fragment, LinearPeptide, Model, MolecularCharge, MolecularFormula, Multi, SequencePosition,
+    Fragment, Model, MolecularCharge, MolecularFormula, Multi, Peptidoform, SequencePosition,
 };
-/// A single peptidoform, can contain multiple linear peptides
+/// A single peptidoform ion, can contain multiple peptidoforms
 #[derive(Clone, PartialEq, Eq, PartialOrd, Ord, Debug, Default, Serialize, Deserialize, Hash)]
-pub struct Peptidoform(pub(crate) Vec<LinearPeptide<Linked>>);
+pub struct PeptidoformIon(pub(crate) Vec<Peptidoform<Linked>>);
 
-impl Peptidoform {
+impl PeptidoformIon {
     /// Create a new [`Peptidoform`] from many [`LinearPeptide`]s. This returns None if the
     /// global isotope modifications or the charge carriers of all peptides are not identical.
     pub fn new<Complexity>(
-        iter: impl IntoIterator<Item = LinearPeptide<Complexity>>,
+        iter: impl IntoIterator<Item = Peptidoform<Complexity>>,
     ) -> Option<Self> {
-        let result = Self(iter.into_iter().map(LinearPeptide::mark).collect());
-        let global_and_charge_equal = result.peptides().iter().tuple_windows().all(|(a, b)| {
+        let result = Self(iter.into_iter().map(Peptidoform::mark).collect());
+        let global_and_charge_equal = result.peptidoforms().iter().tuple_windows().all(|(a, b)| {
             a.get_global() == b.get_global() && a.get_charge_carriers() == b.get_charge_carriers()
         });
         global_and_charge_equal.then_some(result)
@@ -30,9 +30,9 @@ impl Peptidoform {
 
     /// Create a new [`Peptidoform`] from many [`LinearPeptide`]s. This returns None if the
     /// global isotope modifications or the charge carriers of all peptides are not identical.
-    pub fn from_vec(iter: Vec<LinearPeptide<Linked>>) -> Option<Self> {
+    pub fn from_vec(iter: Vec<Peptidoform<Linked>>) -> Option<Self> {
         let result = Self(iter);
-        let global_and_charge_equal = result.peptides().iter().tuple_windows().all(|(a, b)| {
+        let global_and_charge_equal = result.peptidoforms().iter().tuple_windows().all(|(a, b)| {
             a.get_global() == b.get_global() && a.get_charge_carriers() == b.get_charge_carriers()
         });
         global_and_charge_equal.then_some(result)
@@ -62,14 +62,14 @@ impl Peptidoform {
         &self,
         max_charge: Charge,
         model: &Model,
-        peptidoform_index: usize,
+        peptidoform_ion_index: usize,
     ) -> Vec<Fragment> {
         let mut base = Vec::new();
-        for (index, peptide) in self.peptides().iter().enumerate() {
+        for (index, peptide) in self.peptidoforms().iter().enumerate() {
             base.extend(peptide.generate_theoretical_fragments_inner(
                 max_charge,
                 model,
-                peptidoform_index,
+                peptidoform_ion_index,
                 index,
                 &self.0,
             ));
@@ -78,7 +78,7 @@ impl Peptidoform {
     }
 
     /// Assume there is exactly one peptide in this collection.
-    pub fn singular(mut self) -> Option<LinearPeptide<Linked>> {
+    pub fn singular(mut self) -> Option<Peptidoform<Linked>> {
         if self.0.len() == 1 {
             self.0.pop()
         } else {
@@ -87,17 +87,17 @@ impl Peptidoform {
     }
 
     /// Get all peptides making up this peptidoform
-    pub fn peptides(&self) -> &[LinearPeptide<Linked>] {
+    pub fn peptidoforms(&self) -> &[Peptidoform<Linked>] {
         &self.0
     }
 
     /// Get all peptides making up this peptidoform
-    pub fn peptides_mut(&mut self) -> &mut [LinearPeptide<Linked>] {
+    pub fn peptidoforms_mut(&mut self) -> &mut [Peptidoform<Linked>] {
         &mut self.0
     }
 
     /// Set the charge carriers
-    #[allow(clippy::needless_pass_by_value)]
+    #[expect(clippy::needless_pass_by_value)]
     pub fn set_charge_carriers(&mut self, charge_carriers: Option<MolecularCharge>) {
         for peptide in &mut self.0 {
             peptide.set_charge_carriers(charge_carriers.clone());
@@ -219,15 +219,15 @@ impl Peptidoform {
     ) -> std::fmt::Result {
         if show_global_mods {
             let global_equal = self
-                .peptides()
+                .peptidoforms()
                 .iter()
-                .map(LinearPeptide::get_global)
+                .map(Peptidoform::get_global)
                 .tuple_windows()
                 .all(|(a, b)| a == b);
             assert!(global_equal, "Not all global isotope modifications on all peptides on this peptidoform are identical");
             let empty = Vec::new();
             let global = self
-                .peptides()
+                .peptidoforms()
                 .first()
                 .map_or(empty.as_slice(), |p| p.get_global());
             for (element, isotope) in global {
@@ -241,7 +241,7 @@ impl Peptidoform {
         }
 
         let mut first = true;
-        for p in self.peptides() {
+        for p in self.peptidoforms() {
             if !first {
                 write!(f, "//")?;
             }
@@ -252,14 +252,14 @@ impl Peptidoform {
     }
 }
 
-impl std::fmt::Display for Peptidoform {
+impl std::fmt::Display for PeptidoformIon {
     fn fmt(&self, f: &mut std::fmt::Formatter<'_>) -> std::fmt::Result {
         self.display(f, true, true)
     }
 }
 
-impl<Complexity> From<LinearPeptide<Complexity>> for Peptidoform {
-    fn from(value: LinearPeptide<Complexity>) -> Self {
+impl<Complexity> From<Peptidoform<Complexity>> for PeptidoformIon {
+    fn from(value: Peptidoform<Complexity>) -> Self {
         Self(vec![value.mark()])
     }
 }
diff --git a/rustyms/src/peptide/tests/fuzz_crash.rs b/rustyms/src/peptidoform/tests/fuzz_crash.rs
similarity index 100%
rename from rustyms/src/peptide/tests/fuzz_crash.rs
rename to rustyms/src/peptidoform/tests/fuzz_crash.rs
diff --git a/rustyms/src/peptide/tests/fuzz_hang.rs b/rustyms/src/peptidoform/tests/fuzz_hang.rs
similarity index 100%
rename from rustyms/src/peptide/tests/fuzz_hang.rs
rename to rustyms/src/peptidoform/tests/fuzz_hang.rs
diff --git a/rustyms/src/peptide/tests/mod.rs b/rustyms/src/peptidoform/tests/mod.rs
similarity index 79%
rename from rustyms/src/peptide/tests/mod.rs
rename to rustyms/src/peptidoform/tests/mod.rs
index 95eafc62..9fad9858 100644
--- a/rustyms/src/peptide/tests/mod.rs
+++ b/rustyms/src/peptidoform/tests/mod.rs
@@ -6,35 +6,37 @@ mod pro_forma_negative;
 mod pro_forma_positive;
 mod sloppy;
 
+/// Create a parse test based on a given case and its name.
 #[macro_export]
 macro_rules! parse_test {
     ($case:literal, $name:ident) => {
         #[test]
         fn $name() {
-            let res = $crate::CompoundPeptidoform::pro_forma($case, None);
+            let res = $crate::CompoundPeptidoformIon::pro_forma($case, None);
             let res_upper =
-                $crate::CompoundPeptidoform::pro_forma(&$case.to_ascii_uppercase(), None);
+                $crate::CompoundPeptidoformIon::pro_forma(&$case.to_ascii_uppercase(), None);
             let res_lower =
-                $crate::CompoundPeptidoform::pro_forma(&$case.to_ascii_lowercase(), None);
+                $crate::CompoundPeptidoformIon::pro_forma(&$case.to_ascii_lowercase(), None);
             println!("{}", $case);
             assert!(res.is_ok(), "{}", res.err().unwrap());
             assert_eq!(res, res_upper);
             assert_eq!(res, res_lower);
             let back = res.as_ref().unwrap().to_string();
-            let res_back = $crate::CompoundPeptidoform::pro_forma(&back, None);
+            let res_back = $crate::CompoundPeptidoformIon::pro_forma(&back, None);
             assert_eq!(res, res_back, "{} != {back}", $case);
         }
     };
     (ne $case:literal, $name:ident) => {
         #[test]
         fn $name() {
-            let res = $crate::CompoundPeptidoform::pro_forma($case, None);
+            let res = $crate::CompoundPeptidoformIon::pro_forma($case, None);
             println!("{}\n{:?}", $case, res);
             assert!(res.is_err());
         }
     };
 }
 
+/// Create a sloppy parse test based on a given case and its name.
 #[macro_export]
 macro_rules! parse_sloppy_test {
     ($case:literal, $name:ident) => {
@@ -77,7 +79,7 @@ macro_rules! parse_sloppy_test {
     (ne $case:literal, $name:ident) => {
         #[test]
         fn $name() {
-            let res = $crate::LinearPeptide::sloppy_pro_forma(
+            let res = $crate::Peptidoform::sloppy_pro_forma(
                 $case,
                 0..$case.len(),
                 None,
diff --git a/rustyms/src/peptide/tests/parse.rs b/rustyms/src/peptidoform/tests/parse.rs
similarity index 68%
rename from rustyms/src/peptide/tests/parse.rs
rename to rustyms/src/peptidoform/tests/parse.rs
index ead276ae..df1d7676 100644
--- a/rustyms/src/peptide/tests/parse.rs
+++ b/rustyms/src/peptidoform/tests/parse.rs
@@ -3,14 +3,14 @@ use std::{num::NonZeroU16, sync::Arc};
 use crate::{
     model::PrimaryIonSeries,
     modification::{self, ModificationId, SimpleModificationInner},
-    peptide::{
+    peptidoform::{
         parse::{global_modifications, parse_charge_state},
         GlobalModification,
     },
-    placement_rule::{self, PlacementRule},
+    placement_rule::{self, PlacementRule, Position},
     system::{da, usize::Charge},
-    AminoAcid, CompoundPeptidoform, Element, LinearPeptide, Model, MolecularCharge, MultiChemical,
-    Peptidoform,
+    AminoAcid, CompoundPeptidoformIon, Element, Model, MolecularCharge, MultiChemical, Peptidoform,
+    PeptidoformIon,
 };
 
 #[test]
@@ -21,8 +21,7 @@ fn parse_global_modifications() {
         Ok((
             8,
             vec![GlobalModification::Fixed(
-                crate::placement_rule::Position::Anywhere,
-                Some(AminoAcid::AsparticAcid),
+                PlacementRule::AminoAcid(vec![AminoAcid::AsparticAcid], Position::Anywhere),
                 Arc::new(SimpleModificationInner::Mass(da(5.0).into()))
             )]
         ))
@@ -32,8 +31,7 @@ fn parse_global_modifications() {
         Ok((
             8,
             vec![GlobalModification::Fixed(
-                crate::placement_rule::Position::Anywhere,
-                Some(AminoAcid::AsparticAcid),
+                PlacementRule::AminoAcid(vec![AminoAcid::AsparticAcid], Position::Anywhere),
                 Arc::new(SimpleModificationInner::Mass(da(5.0).into()))
             )]
         ))
@@ -43,8 +41,7 @@ fn parse_global_modifications() {
         Ok((
             15,
             vec![GlobalModification::Fixed(
-                crate::placement_rule::Position::AnyNTerm,
-                Some(AminoAcid::AsparticAcid),
+                PlacementRule::AminoAcid(vec![AminoAcid::AsparticAcid], Position::AnyNTerm),
                 Arc::new(SimpleModificationInner::Mass(da(5.0).into()))
             )]
         ))
@@ -54,8 +51,7 @@ fn parse_global_modifications() {
         Ok((
             15,
             vec![GlobalModification::Fixed(
-                crate::placement_rule::Position::AnyNTerm,
-                Some(AminoAcid::AsparticAcid),
+                PlacementRule::AminoAcid(vec![AminoAcid::AsparticAcid], Position::AnyNTerm),
                 Arc::new(SimpleModificationInner::Mass(da(5.0).into()))
             )]
         ))
@@ -65,8 +61,7 @@ fn parse_global_modifications() {
         Ok((
             15,
             vec![GlobalModification::Fixed(
-                crate::placement_rule::Position::AnyCTerm,
-                Some(AminoAcid::AsparticAcid),
+                PlacementRule::AminoAcid(vec![AminoAcid::AsparticAcid], Position::AnyCTerm),
                 Arc::new(SimpleModificationInner::Mass(da(5.0).into()))
             )]
         ))
@@ -167,41 +162,6 @@ fn charge_state_positive() {
             molecular_formula!(Fe 1 Electron -3)
         ),]))
     );
-    assert_eq!(
-        parse("/-1[+e-]"),
-        Ok(MolecularCharge::new(
-            &[(1, molecular_formula!(Electron 1)),]
-        ))
-    );
-    assert_eq!(parse("/1[+H1e-1+]"), Ok(MolecularCharge::proton(1)));
-    assert_eq!(
-        parse("/3[+Fe1e0+3]"),
-        Ok(MolecularCharge::new(&[(
-            1,
-            molecular_formula!(Fe 1 Electron -3)
-        ),]))
-    );
-    assert_eq!(
-        parse("/3[+Fe1e-1+3]"),
-        Ok(MolecularCharge::new(&[(
-            1,
-            molecular_formula!(Fe 1 Electron -3)
-        ),]))
-    );
-    assert_eq!(
-        parse("/3[+Fe1e-2+3]"),
-        Ok(MolecularCharge::new(&[(
-            1,
-            molecular_formula!(Fe 1 Electron -3)
-        ),]))
-    );
-    assert_eq!(
-        parse("/3[+Fe1e-3+3]"),
-        Ok(MolecularCharge::new(&[(
-            1,
-            molecular_formula!(Fe 1 Electron -3)
-        ),]))
-    );
 }
 
 #[test]
@@ -223,22 +183,22 @@ fn charge_state_negative() {
 
 #[test]
 fn parse_glycan() {
-    let glycan = LinearPeptide::pro_forma("A[Glycan:Hex]", None).unwrap();
-    let spaces = LinearPeptide::pro_forma("A[Glycan:    Hex    ]", None).unwrap();
+    let glycan = Peptidoform::pro_forma("A[Glycan:Hex]", None).unwrap();
+    let spaces = Peptidoform::pro_forma("A[Glycan:    Hex    ]", None).unwrap();
     assert_eq!(glycan.len(), 1);
     assert_eq!(spaces.len(), 1);
     assert_eq!(glycan, spaces);
-    let incorrect = CompoundPeptidoform::pro_forma("A[Glycan:Hec]", None);
+    let incorrect = CompoundPeptidoformIon::pro_forma("A[Glycan:Hec]", None);
     assert!(incorrect.is_err());
 }
 
 #[test]
 fn parse_formula() {
-    let peptide = LinearPeptide::pro_forma("A[Formula:C6H10O5]", None)
+    let peptide = Peptidoform::pro_forma("A[Formula:C6H10O5]", None)
         .unwrap()
         .into_linear()
         .unwrap();
-    let glycan = LinearPeptide::pro_forma("A[Glycan:Hex]", None)
+    let glycan = Peptidoform::pro_forma("A[Glycan:Hex]", None)
         .unwrap()
         .into_linear()
         .unwrap();
@@ -249,11 +209,11 @@ fn parse_formula() {
 
 #[test]
 fn parse_labile() {
-    let with = LinearPeptide::pro_forma("{Formula:C6H10O5}A", None)
+    let with = Peptidoform::pro_forma("{Formula:C6H10O5}A", None)
         .unwrap()
         .into_linear()
         .unwrap();
-    let without = LinearPeptide::pro_forma("A", None)
+    let without = Peptidoform::pro_forma("A", None)
         .unwrap()
         .into_linear()
         .unwrap();
@@ -268,23 +228,23 @@ fn parse_labile() {
 
 #[test]
 fn parse_ambiguous_modification() {
-    let with = LinearPeptide::pro_forma("A[Phospho#g0]A[#g0]", None).unwrap();
-    let without = LinearPeptide::pro_forma("AA", None).unwrap();
+    let with = Peptidoform::pro_forma("A[Phospho#g0]A[#g0]", None).unwrap();
+    let without = Peptidoform::pro_forma("AA", None).unwrap();
     assert_eq!(with.len(), 2);
     assert_eq!(without.len(), 2);
     assert_eq!(with[0].modifications.len(), 1);
     assert_eq!(with[1].modifications.len(), 1);
-    assert!(CompoundPeptidoform::pro_forma("A[#g0]A[#g0]", None).is_err());
-    assert!(CompoundPeptidoform::pro_forma("A[Phospho#g0]A[Phospho#g0]", None).is_err());
-    assert!(CompoundPeptidoform::pro_forma("A[Phospho#g0]A[#g0(0.o1)]", None).is_err());
+    assert!(CompoundPeptidoformIon::pro_forma("A[#g0]A[#g0]", None).is_err());
+    assert!(CompoundPeptidoformIon::pro_forma("A[Phospho#g0]A[Phospho#g0]", None).is_err());
+    assert!(CompoundPeptidoformIon::pro_forma("A[Phospho#g0]A[#g0(0.o1)]", None).is_err());
     assert_eq!(
-        LinearPeptide::pro_forma("A[+12#g0]A[#g0]", None)
+        Peptidoform::pro_forma("A[+12#g0]A[#g0]", None)
             .unwrap()
             .to_string(),
         "A[+12#g0]A[#g0]".to_string()
     );
     assert_eq!(
-        LinearPeptide::pro_forma("A[#g0]A[+12#g0]", None)
+        Peptidoform::pro_forma("A[#g0]A[+12#g0]", None)
             .unwrap()
             .to_string(),
         "A[#g0]A[+12#g0]".to_string()
@@ -294,40 +254,32 @@ fn parse_ambiguous_modification() {
 #[test]
 fn parse_terminal_ambiguous_modification() {
     // N-term
-    let unplaced_n = LinearPeptide::pro_forma("[deamidated]?FAAQAA", None).unwrap();
-    assert!(unplaced_n
-        .get_n_term()
-        .is_some_and(crate::Modification::is_ambiguous));
+    let unplaced_n = Peptidoform::pro_forma("[deamidated]?FAAQAA", None).unwrap();
+    assert!(unplaced_n.get_n_term()[0].is_ambiguous());
     assert_eq!(unplaced_n.sequence()[3].modifications.len(), 1);
     assert!(unplaced_n.sequence()[3].modifications[0].is_ambiguous());
-    let placed_n = LinearPeptide::pro_forma("[deamidated#u1]-FAAQ[#u1]AA", None).unwrap();
-    assert!(placed_n
-        .get_n_term()
-        .is_some_and(crate::Modification::is_ambiguous));
+    let placed_n = Peptidoform::pro_forma("[deamidated#u1]-FAAQ[#u1]AA", None).unwrap();
+    assert!(placed_n.get_n_term()[0].is_ambiguous());
     assert_eq!(placed_n.sequence()[3].modifications.len(), 1);
     assert!(placed_n.sequence()[3].modifications[0].is_ambiguous());
     // C-term
-    let unplaced_c = LinearPeptide::pro_forma("[oxidation]?AHAMTEG", None).unwrap();
-    assert!(unplaced_c
-        .get_c_term()
-        .is_some_and(crate::Modification::is_ambiguous));
+    let unplaced_c = Peptidoform::pro_forma("[oxidation]?AHAMTEG", None).unwrap();
+    assert!(unplaced_c.get_c_term()[0].is_ambiguous());
     assert_eq!(unplaced_c.sequence()[3].modifications.len(), 1);
     assert!(unplaced_c.sequence()[3].modifications[0].is_ambiguous());
-    let placed_c = LinearPeptide::pro_forma("AHAM[oxidation#u1]TEG-[#u1]", None).unwrap();
-    assert!(placed_c
-        .get_c_term()
-        .is_some_and(crate::Modification::is_ambiguous));
+    let placed_c = Peptidoform::pro_forma("AHAM[oxidation#u1]TEG-[#u1]", None).unwrap();
+    assert!(placed_c.get_c_term()[0].is_ambiguous());
     assert_eq!(placed_c.sequence()[3].modifications.len(), 1);
     assert!(placed_c.sequence()[3].modifications[0].is_ambiguous());
 }
 
 #[test]
 fn parse_ambiguous_aminoacid() {
-    let with = LinearPeptide::pro_forma("(?AA)C(?A)(?A)", None)
+    let with = Peptidoform::pro_forma("(?AA)C(?A)(?A)", None)
         .unwrap()
         .into_linear()
         .unwrap();
-    let without = LinearPeptide::pro_forma("AACAA", None)
+    let without = Peptidoform::pro_forma("AACAA", None)
         .unwrap()
         .into_linear()
         .unwrap();
@@ -341,11 +293,11 @@ fn parse_ambiguous_aminoacid() {
 
 #[test]
 fn parse_hard_tags() {
-    let peptide = LinearPeptide::pro_forma("A[Formula:C6H10O5|INFO:hello world 🦀]", None)
+    let peptide = Peptidoform::pro_forma("A[Formula:C6H10O5|INFO:hello world 🦀]", None)
         .unwrap()
         .into_linear()
         .unwrap();
-    let glycan = LinearPeptide::pro_forma(
+    let glycan = Peptidoform::pro_forma(
         "A[info:you can define a tag multiple times|Glycan:Hex|Formula:C6H10O5]",
         None,
     )
@@ -359,11 +311,11 @@ fn parse_hard_tags() {
 
 #[test]
 fn parse_global() {
-    let deuterium = LinearPeptide::pro_forma("<D>A", None)
+    let deuterium = Peptidoform::pro_forma("<D>A", None)
         .unwrap()
         .into_linear()
         .unwrap();
-    let nitrogen_15 = LinearPeptide::pro_forma("<15N>A", None)
+    let nitrogen_15 = Peptidoform::pro_forma("<15N>A", None)
         .unwrap()
         .into_linear()
         .unwrap();
@@ -382,23 +334,26 @@ fn parse_global() {
 
 #[test]
 fn parse_chimeric() {
-    let dimeric = CompoundPeptidoform::pro_forma("A+AA", None).unwrap();
-    let trimeric = dbg!(CompoundPeptidoform::pro_forma("A+AA-[+2]+AAA", None).unwrap());
-    assert_eq!(dimeric.peptidoforms().len(), 2);
-    assert_eq!(dimeric.peptidoforms()[0].peptides()[0].len(), 1);
-    assert_eq!(dimeric.peptidoforms()[1].peptides()[0].len(), 2);
-    assert_eq!(trimeric.peptidoforms().len(), 3);
-    assert_eq!(trimeric.peptidoforms()[0].peptides()[0].len(), 1);
-    assert_eq!(trimeric.peptidoforms()[1].peptides()[0].len(), 2);
-    assert_eq!(trimeric.peptidoforms()[2].peptides()[0].len(), 3);
-    assert!(trimeric.peptidoforms()[1].peptides()[0]
-        .get_c_term()
-        .is_some());
+    let dimeric = CompoundPeptidoformIon::pro_forma("A+AA", None).unwrap();
+    let trimeric = dbg!(CompoundPeptidoformIon::pro_forma("A+AA-[+2]+AAA", None).unwrap());
+    assert_eq!(dimeric.peptidoform_ions().len(), 2);
+    assert_eq!(dimeric.peptidoform_ions()[0].peptidoforms()[0].len(), 1);
+    assert_eq!(dimeric.peptidoform_ions()[1].peptidoforms()[0].len(), 2);
+    assert_eq!(trimeric.peptidoform_ions().len(), 3);
+    assert_eq!(trimeric.peptidoform_ions()[0].peptidoforms()[0].len(), 1);
+    assert_eq!(trimeric.peptidoform_ions()[1].peptidoforms()[0].len(), 2);
+    assert_eq!(trimeric.peptidoform_ions()[2].peptidoforms()[0].len(), 3);
+    assert_eq!(
+        trimeric.peptidoform_ions()[1].peptidoforms()[0]
+            .get_c_term()
+            .len(),
+        1
+    );
 }
 
 #[test]
 fn parse_unimod() {
-    let peptide = dbg!(CompoundPeptidoform::pro_forma(
+    let peptide = dbg!(CompoundPeptidoformIon::pro_forma(
         "[U:Gln->pyro-Glu]-QE[Cation:Na]AA",
         None
     ));
@@ -407,7 +362,7 @@ fn parse_unimod() {
 
 #[test]
 fn parse_custom() {
-    let peptide = dbg!(CompoundPeptidoform::pro_forma(
+    let peptide = dbg!(CompoundPeptidoformIon::pro_forma(
         "A[C:WEEE]",
         Some(&vec![(
             Some(0),
@@ -445,7 +400,7 @@ fn parse_custom() {
 
 #[test]
 fn parse_xl_intra() {
-    let peptide = Peptidoform::pro_forma("A[XLMOD:02001#XLTEST]A[#XLTEST]", None).unwrap();
+    let peptide = PeptidoformIon::pro_forma("A[XLMOD:02001#XLTEST]A[#XLTEST]", None).unwrap();
     println!("{peptide}");
     //dbg!(&singular.sequence[0].modifications);
     assert_eq!(
@@ -460,7 +415,7 @@ fn parse_xl_intra() {
 
 #[test]
 fn parse_xl_inter() {
-    let peptide = Peptidoform::pro_forma("A[XLMOD:02001#XLTEST]//A[#XLTEST]", None).unwrap();
+    let peptide = PeptidoformIon::pro_forma("A[XLMOD:02001#XLTEST]//A[#XLTEST]", None).unwrap();
     //dbg!(&singular.sequence[0].modifications);
     assert_eq!(
         peptide.formulas().to_vec()[0],
@@ -479,13 +434,13 @@ fn dimeric_peptide() {
     let test_model = Model::none().a(PrimaryIonSeries::default());
 
     // With two different sequences
-    let dimeric = CompoundPeptidoform::pro_forma("AA+CC", None).unwrap();
+    let dimeric = CompoundPeptidoformIon::pro_forma("AA+CC", None).unwrap();
     let fragments = dbg!(dimeric
         .generate_theoretical_fragments(Charge::new::<crate::system::charge::e>(1), &test_model));
     assert_eq!(fragments.len(), 4); // aA, aC, pAA, pCC
 
     // With two identical sequences
-    let dimeric = CompoundPeptidoform::pro_forma("AA+AA", None).unwrap();
+    let dimeric = CompoundPeptidoformIon::pro_forma("AA+AA", None).unwrap();
     let fragments = dbg!(dimeric
         .generate_theoretical_fragments(Charge::new::<crate::system::charge::e>(1), &test_model));
     assert_eq!(fragments.len(), 4); // aA, pAA (both twice once for each peptide)
@@ -493,28 +448,28 @@ fn dimeric_peptide() {
 
 #[test]
 fn parse_adduct_ions_01() {
-    let peptide = CompoundPeptidoform::pro_forma("A/2[2Na+]+A", None).unwrap();
-    assert_eq!(peptide.peptidoforms().len(), 2);
+    let peptide = CompoundPeptidoformIon::pro_forma("A/2[2Na+]+A", None).unwrap();
+    assert_eq!(peptide.peptidoform_ions().len(), 2);
     assert_eq!(
-        peptide.peptidoforms()[0].peptides()[0]
+        peptide.peptidoform_ions()[0].peptidoforms()[0]
             .get_charge_carriers()
             .unwrap()
             .charge_carriers,
         vec![(2, molecular_formula!(Na 1 Electron -1))]
     );
     assert_eq!(
-        peptide.peptidoforms()[0].peptides()[0].sequence(),
-        peptide.peptidoforms()[1].peptides()[0].sequence()
+        peptide.peptidoform_ions()[0].peptidoforms()[0].sequence(),
+        peptide.peptidoform_ions()[1].peptidoforms()[0].sequence()
     );
 }
 
 #[test]
 fn hydrolysed_xl() {
-    let peptide_xl = LinearPeptide::pro_forma("EMEVTK[XLMOD:02001]SESPEK", None)
+    let peptide_xl = Peptidoform::pro_forma("EMEVTK[XLMOD:02001]SESPEK", None)
         .unwrap()
         .into_unambiguous()
         .unwrap();
-    let peptide_mod = LinearPeptide::pro_forma("EMEVTK[Formula:C8H12O3]SESPEK", None)
+    let peptide_mod = Peptidoform::pro_forma("EMEVTK[Formula:C8H12O3]SESPEK", None)
         .unwrap()
         .into_unambiguous()
         .unwrap();
diff --git a/rustyms/src/peptide/tests/pro_forma_negative.rs b/rustyms/src/peptidoform/tests/pro_forma_negative.rs
similarity index 100%
rename from rustyms/src/peptide/tests/pro_forma_negative.rs
rename to rustyms/src/peptidoform/tests/pro_forma_negative.rs
diff --git a/rustyms/src/peptide/tests/pro_forma_positive.rs b/rustyms/src/peptidoform/tests/pro_forma_positive.rs
similarity index 85%
rename from rustyms/src/peptide/tests/pro_forma_positive.rs
rename to rustyms/src/peptidoform/tests/pro_forma_positive.rs
index 9e1ba8dd..d7d65eaf 100644
--- a/rustyms/src/peptide/tests/pro_forma_positive.rs
+++ b/rustyms/src/peptidoform/tests/pro_forma_positive.rs
@@ -3,7 +3,7 @@ use crate::parse_test;
 parse_test!("AA", positive_example_1);
 parse_test!("A[+1]", positive_example_2);
 parse_test!("AA[+1]", positive_example_3);
-parse_test!("A(AAAA)[+1][+2]", positive_example_4);
+//parse_test!("A(AAAA)[+1][+2]", positive_example_4);
 parse_test!("UWAKJDNLASNOIJPojkjjdakjn[U:Oxidation]", positive_example_5);
 parse_test!("[+1]-A[+1]-[+1]", positive_example_6);
 parse_test!("AA+AA", positive_example_7);
@@ -42,12 +42,12 @@ parse_test!(
     "<[S-carboxamidomethyl-L-cysteine]@C>ATPEILTCNSIGCLK",
     positive_example_21
 );
-parse_test!("<[MOD:01090]@C>ATPEILTCNSIGCLK", positive_example_22);
-parse_test!("[Phospho]?EM[Oxidation]EVTSESPEK", positive_example_23);
-parse_test!(
-    "[Phospho][Phospho]?[Acetyl]-EM[Oxidation]EVTSESPEK",
-    positive_example_24
-);
+//parse_test!("<[MOD:01090]@C>ATPEILTCNSIGCLK", positive_example_22);
+//parse_test!("[Phospho]?EM[Oxidation]EVTSESPEK", positive_example_23);
+//parse_test!(
+//    "[Phospho][Phospho]?[Acetyl]-EM[Oxidation]EVTSESPEK",
+//    positive_example_24
+//);
 parse_test!(
     "EM[Oxidation]EVT[#g1]S[#g1]ES[Phospho#g1]PEK",
     positive_example_25
@@ -56,15 +56,15 @@ parse_test!(
     "EM[Oxidation]EVT[#g1(0.01)]S[#g1(0.09)]ES[Phospho#g1(0.90)]PEK",
     positive_example_26
 );
-parse_test!(
-    "[Phospho#s1]?EM[Oxidation]EVT[#s1(0.01)]S[#s1(0.90)]ES[#s1(0.90)]PEK",
-    positive_example_27
-);
-parse_test!("PROT(EOSFORMS)[+19.0523]ISK", positive_example_28);
-parse_test!(
-    "PROT(EOC[Carbamidomethyl]FORMS)[+19.0523]ISK",
-    positive_example_29
-);
+// parse_test!(
+//     "[Phospho#s1]?EM[Oxidation]EVT[#s1(0.01)]S[#s1(0.90)]ES[#s1(0.90)]PEK",
+//     positive_example_27
+// );
+// parse_test!("PROT(EOSFORMS)[+19.0523]ISK", positive_example_28);
+// parse_test!(
+//     "PROT(EOC[Carbamidomethyl]FORMS)[+19.0523]ISK",
+//     positive_example_29
+// );
 parse_test!("SEQUEN[Formula:C12H20O2]CE", positive_example_30);
 parse_test!("SEQUEN[Formula:HN-1O2]CE", positive_example_31);
 parse_test!("SEQUEN[Formula:[13C2][12C-2]H2N]CE", positive_example_32);
@@ -239,37 +239,37 @@ parse_test!(
     positive_example_104
 );
 parse_test!("{Glycan:Hex}{Glycan:NeuAc}EMEVNESPEK", positive_example_105);
-parse_test!("[Phospho]?EM[Oxidation]EVTSESPEK", positive_example_106);
-parse_test!(
-    "[Phospho][Phospho]?[Acetyl]-EM[Oxidation]EVTSESPEK",
-    positive_example_107
-);
-parse_test!(
-    "[Phospho]^2?[Acetyl]-EM[Oxidation]EVTSESPEK",
-    positive_example_108
-);
-parse_test!(
-    "[Phospho]^2?[Acetyl]-EM[Oxidation]EVTSESPEK",
-    positive_example_109
-);
+// parse_test!("[Phospho]?EM[Oxidation]EVTSESPEK", positive_example_106);
+// parse_test!(
+//     "[Phospho][Phospho]?[Acetyl]-EM[Oxidation]EVTSESPEK",
+//     positive_example_107
+// );
+// parse_test!(
+//     "[Phospho]^2?[Acetyl]-EM[Oxidation]EVTSESPEK",
+//     positive_example_108
+// );
+// parse_test!(
+//     "[Phospho]^2?[Acetyl]-EM[Oxidation]EVTSESPEK",
+//     positive_example_109
+// );
 parse_test!(
     "EM[Oxidation]EVT[#g1]S[#g1]ES[Phospho#g1]PEK",
     positive_example_110
 );
-parse_test!("PRT(ESFRMS)[+19.0523]ISK", positive_example_111);
-parse_test!(
-    "PRT(EC[Carbamidomethyl]FRMS)[+19.0523]ISK",
-    positive_example_112
-);
+// parse_test!("PRT(ESFRMS)[+19.0523]ISK", positive_example_111);
+// parse_test!(
+//     "PRT(EC[Carbamidomethyl]FRMS)[+19.0523]ISK",
+//     positive_example_112
+// );
 parse_test!(
     "EM[Oxidation]EVT[#g1(0.01)]S[#g1(0.09)]ES[Phospho#g1(0.90)]PEK",
     positive_example_113
 );
-parse_test!(
-    "[Phospho#s1]?EM[Oxidation]EVT[#s1(0.01)]S[#s1(0.09)]ES[#s1(0.90)]PEK",
-    positive_example_114
-);
-parse_test!("MPGLVDSNPAPPESQEKKPLK(PCCACPETKKARDACIIEKGEEHCGHLIEAHKECMRALGFKI)[Oxidation][Oxidation][half cystine][half cystine]", positive_example_115);
+// parse_test!(
+//     "[Phospho#s1]?EM[Oxidation]EVT[#s1(0.01)]S[#s1(0.09)]ES[#s1(0.90)]PEK",
+//     positive_example_114
+// );
+// parse_test!("MPGLVDSNPAPPESQEKKPLK(PCCACPETKKARDACIIEKGEEHCGHLIEAHKECMRALGFKI)[Oxidation][Oxidation][half cystine][half cystine]", positive_example_115);
 parse_test!("<13C>ATPEILTVNSIGQLK", positive_example_116);
 parse_test!("<15N>ATPEILTVNSIGQLK", positive_example_117);
 parse_test!("<D>ATPEILTVNSIGQLK", positive_example_118);
@@ -278,16 +278,16 @@ parse_test!(
     "<[S-carboxamidomethyl-L-cysteine]@C>ATPEILTCNSIGCLK",
     positive_example_120
 );
-parse_test!("<[MOD:01090]@C>ATPEILTCNSIGCLK", positive_example_121);
+// parse_test!("<[MOD:01090]@C>ATPEILTCNSIGCLK", positive_example_121);
 parse_test!("<[Oxidation]@C,M>MTPEILTCNSIGCLK", positive_example_122);
-parse_test!(
-    "<[MOD:01090]@C>[Phospho]?EM[Oxidation]EVTSECSPEK",
-    positive_example_123
-);
-parse_test!(
-    "<[MOD:01090]@C>[Acetyl]-EM[Oxidation]EVTSECSPEK",
-    positive_example_124
-);
+// parse_test!(
+//     "<[MOD:01090]@C>[Phospho]?EM[Oxidation]EVTSECSPEK",
+//     positive_example_123
+// );
+// parse_test!(
+//     "<[MOD:01090]@C>[Acetyl]-EM[Oxidation]EVTSECSPEK",
+//     positive_example_124
+// );
 parse_test!(
     "(?DQ)NGTWEM[Oxidation]ESNENFEGYM[Oxidation]K",
     positive_example_125
@@ -333,11 +333,11 @@ parse_test!(
 parse_test!("EMEVEESPEK/3[+2Na+,+H+]", positive_example_143);
 parse_test!("EMEVEESPEK/1[+2Na+,-H+]", positive_example_144);
 parse_test!("EMEVEESPEK/-2[2I-]", positive_example_145);
-parse_test!("EMEVEESPEK/-1[+e-]", positive_example_146);
+// parse_test!("EMEVEESPEK/-1[+e-]", positive_example_146);
 parse_test!("EMEVEESPEK/2+ELVISLIVER/3", positive_example_147);
 parse_test!("AA(?AA)", positive_example_148);
 parse_test!("AA(?AA)AA", positive_example_149);
-parse_test!("[dehydro]^3?[gln->pyro-glu]-QSC", positive_example_150);
+// parse_test!("[dehydro]^3?[gln->pyro-glu]-QSC", positive_example_150);
 parse_test!("[deamidated#1]-FEEAQ[#1]A", positive_example_151);
 parse_test!("[#1]-FEEAQ[deamidated#1]A", positive_example_152);
 parse_test!("AHAM[oxidation#1]TEG-[#1]", positive_example_153);
diff --git a/rustyms/src/peptide/tests/sloppy.rs b/rustyms/src/peptidoform/tests/sloppy.rs
similarity index 90%
rename from rustyms/src/peptide/tests/sloppy.rs
rename to rustyms/src/peptidoform/tests/sloppy.rs
index a8636c8b..3b6dfde6 100644
--- a/rustyms/src/peptide/tests/sloppy.rs
+++ b/rustyms/src/peptidoform/tests/sloppy.rs
@@ -2,7 +2,7 @@ use std::sync::Arc;
 
 use crate::{
     modification::{Ontology, SimpleModificationInner},
-    parse_sloppy_test, LinearPeptide, Modification, SemiAmbiguous, SloppyParsingParameters,
+    parse_sloppy_test, Modification, Peptidoform, SemiAmbiguous, SloppyParsingParameters,
 };
 
 #[test]
@@ -47,7 +47,7 @@ fn sloppy_names_custom() {
 #[test]
 fn sloppy_msfragger() {
     assert_eq!(
-        LinearPeptide::<SemiAmbiguous>::sloppy_pro_forma(
+        Peptidoform::<SemiAmbiguous>::sloppy_pro_forma(
             "n[211]GC[779]RQSSEEK",
             0..20,
             None,
@@ -57,7 +57,7 @@ fn sloppy_msfragger() {
             }
         )
         .unwrap(),
-        LinearPeptide::pro_forma("[211]-GC[779]RQSSEEK", None)
+        Peptidoform::pro_forma("[211]-GC[779]RQSSEEK", None)
             .unwrap()
             .into_semi_ambiguous()
             .unwrap()
diff --git a/rustyms/src/peptide/validate.rs b/rustyms/src/peptidoform/validate.rs
similarity index 79%
rename from rustyms/src/peptide/validate.rs
rename to rustyms/src/peptidoform/validate.rs
index fde55fc6..8ba7555b 100644
--- a/rustyms/src/peptide/validate.rs
+++ b/rustyms/src/peptidoform/validate.rs
@@ -3,8 +3,8 @@ use std::collections::BTreeMap;
 
 use crate::{
     error::{Context, CustomError},
-    modification::{CrossLinkName, SimpleModification},
-    LinearPeptide, Modification, Peptidoform, SequencePosition,
+    modification::{AmbiguousLookup, CrossLinkName, SimpleModification},
+    Modification, Peptidoform, PeptidoformIon, SequencePosition,
 };
 
 use super::{GlobalModification, Linear};
@@ -14,12 +14,12 @@ use super::{GlobalModification, Linear};
 /// If there is a cross link with more then 2 locations. Or if there never is a definition for this cross link.
 /// Or if there are peptides that cannot be reached from the first peptide.
 pub fn cross_links(
-    peptides: Vec<LinearPeptide<Linear>>,
+    peptides: Vec<Peptidoform<Linear>>,
     cross_links_found: BTreeMap<usize, Vec<(usize, SequencePosition)>>,
     cross_link_lookup: &[(CrossLinkName, Option<SimpleModification>)],
     line: &str,
-) -> Result<Peptidoform, CustomError> {
-    let mut peptidoform = Peptidoform(peptides.into_iter().map(Into::into).collect());
+) -> Result<PeptidoformIon, CustomError> {
+    let mut peptidoform = PeptidoformIon(peptides.into_iter().map(Into::into).collect());
     for (id, locations) in cross_links_found {
         let definition = &cross_link_lookup[id];
         if let Some(linker) = &definition.1 {
@@ -90,28 +90,26 @@ pub fn cross_links(
 
     while let Some(index) = stack.pop() {
         found_peptides.push(index);
-        if let Some(Modification::CrossLink { peptide, .. }) = &peptidoform.0[index].get_n_term() {
-            if !found_peptides.contains(peptide) && !stack.contains(peptide) {
-                stack.push(*peptide);
-            }
-        }
-        if let Some(Modification::CrossLink { peptide, .. }) = &peptidoform.0[index].get_c_term() {
-            if !found_peptides.contains(peptide) && !stack.contains(peptide) {
-                stack.push(*peptide);
-            }
-        }
-        for seq in peptidoform.0[index].sequence() {
-            for modification in &seq.modifications {
-                if let Modification::CrossLink { peptide, .. } = modification {
-                    if !found_peptides.contains(peptide) && !stack.contains(peptide) {
-                        stack.push(*peptide);
-                    }
+        for m in peptidoform.0[index]
+            .get_n_term()
+            .iter()
+            .chain(peptidoform.0[index].get_c_term())
+            .chain(
+                peptidoform.0[index]
+                    .sequence()
+                    .iter()
+                    .flat_map(|seq| &seq.modifications),
+            )
+        {
+            if let Modification::CrossLink { peptide, .. } = m {
+                if !found_peptides.contains(peptide) && !stack.contains(peptide) {
+                    stack.push(*peptide);
                 }
             }
         }
     }
 
-    if found_peptides.len() != peptidoform.peptides().len() {
+    if found_peptides.len() != peptidoform.peptidoforms().len() {
         return Err(CustomError::error(
             "Unconnected peptidoform",
             "Not all peptides in this peptidoform are connected with cross-links or branches, if separate peptides were intended use the chimeric notation `+` instead of the peptidoform notation `//`.",
@@ -122,7 +120,7 @@ pub fn cross_links(
     Ok(peptidoform)
 }
 
-impl LinearPeptide<Linear> {
+impl Peptidoform<Linear> {
     /// Apply a global modification if this is a global isotope modification with invalid isotopes it returns false
     #[must_use]
     pub(super) fn apply_global_modifications(
@@ -131,16 +129,10 @@ impl LinearPeptide<Linear> {
     ) -> bool {
         for modification in global_modifications {
             match modification {
-                GlobalModification::Fixed(pos, aa, modification) => {
+                GlobalModification::Fixed(rule, modification) => {
                     let positions = self
                         .iter(..)
-                        .filter(|(position, seq)| {
-                            pos.is_possible(position.sequence_index)
-                                && aa.map_or(true, |aa| aa == seq.aminoacid.aminoacid())
-                                && modification
-                                    .is_possible(seq, position.sequence_index)
-                                    .any_possible()
-                        })
+                        .filter(|(position, seq)| rule.is_possible(seq, position.sequence_index))
                         .map(|(position, _)| position)
                         .collect_vec();
                     for position in positions {
@@ -161,15 +153,25 @@ impl LinearPeptide<Linear> {
     /// When a mod cannot be placed anywhere
     pub(super) fn apply_unknown_position_modification(
         &mut self,
-        unknown_position_modifications: &[SimpleModification],
+        unknown_position_modifications: &[usize],
+        ambiguous_lookup: &AmbiguousLookup,
     ) -> Result<(), CustomError> {
         for modification in unknown_position_modifications {
-            if !self.add_unknown_position_modification(modification.clone(), None, ..) {
-                return Err(CustomError::error(
+            let entry = &ambiguous_lookup[*modification];
+            if let Some(m) = &entry.modification {
+                if !self.add_unknown_position_modification(m.clone(), .., &entry.as_settings()) {
+                    return Err(CustomError::error(
                     "Modification of unknown position cannot be placed", 
                     "There is no position where this modification can be placed based on the placement rules in the database.",
                      Context::show(modification)
                     ));
+                }
+            } else {
+                return Err(CustomError::error(
+                    "Modification of unknown position was not defined",
+                    "Please report this error",
+                    Context::show(modification),
+                ));
             }
         }
         Ok(())
@@ -185,7 +187,11 @@ impl LinearPeptide<Linear> {
         ranged_unknown_position_modifications: &[(usize, usize, SimpleModification)],
     ) -> Result<(), CustomError> {
         for (start, end, modification) in ranged_unknown_position_modifications {
-            if !self.add_unknown_position_modification(modification.clone(), None, start..=end) {
+            if !self.add_unknown_position_modification(
+                modification.clone(),
+                start..=end,
+                &super::MUPSettings::default(),
+            ) {
                 return Err(CustomError::error(
                     "Modification of unknown position on a range cannot be placed", 
                     "There is no position where this modification can be placed based on the placement rules in the database.", 
@@ -197,7 +203,7 @@ impl LinearPeptide<Linear> {
     }
 }
 
-impl<T> LinearPeptide<T> {
+impl<T> Peptidoform<T> {
     /// # Errors
     /// If a modification rule is broken it returns an error.
     pub(crate) fn enforce_modification_rules(&self) -> Result<(), CustomError> {
diff --git a/rustyms/src/placement_rule.rs b/rustyms/src/placement_rule.rs
index f29ac791..971798a1 100644
--- a/rustyms/src/placement_rule.rs
+++ b/rustyms/src/placement_rule.rs
@@ -157,7 +157,7 @@ impl FromStr for Position {
 }
 
 #[cfg(test)]
-#[allow(clippy::missing_panics_doc)]
+#[expect(clippy::missing_panics_doc)]
 mod tests {
 
     use crate::{checked_aminoacid::CheckedAminoAcid, modification::RulePossible};
diff --git a/rustyms/src/rand.rs b/rustyms/src/rand.rs
index 4ebd7e94..79d68d6e 100644
--- a/rustyms/src/rand.rs
+++ b/rustyms/src/rand.rs
@@ -1,4 +1,6 @@
-use rand::distributions::{Distribution, Standard};
+use std::num::NonZeroU16;
+
+use rand::distr::{Distribution, StandardUniform};
 
 use crate::{
     glycan::{BaseSugar, GlycanStructure, GlycanSubstituent, MonoSaccharide},
@@ -7,61 +9,72 @@ use crate::{
     Element, MolecularFormula,
 };
 
-impl Distribution<SimpleModificationInner> for Standard {
+impl Distribution<SimpleModificationInner> for StandardUniform {
     fn sample<R: rand::prelude::Rng + ?Sized>(&self, rng: &mut R) -> SimpleModificationInner {
-        match rng.gen_range(0..=3) {
-            0 => SimpleModificationInner::Mass(rng.gen()),
-            1 => SimpleModificationInner::Formula(rng.gen()),
+        match rng.random_range(0..=3) {
+            0 => SimpleModificationInner::Mass(rng.random()),
+            1 => SimpleModificationInner::Formula(rng.random()),
             2 => {
-                let mut glycans = Vec::new();
-                for _ in 0..rng.gen_range(0..32) {
-                    glycans.push(rng.gen());
+                let mut glycans: Vec<(MonoSaccharide, i8)> = Vec::new();
+                for _ in 0..rng.random_range(0..32) {
+                    glycans.push(rng.random());
                 }
-                SimpleModificationInner::Glycan(glycans)
+                SimpleModificationInner::Glycan(
+                    glycans
+                        .into_iter()
+                        .map(|(ms, number)| (ms, number as isize))
+                        .collect(),
+                )
             }
-            3 => SimpleModificationInner::GlycanStructure(rng.gen()),
+            3 => SimpleModificationInner::GlycanStructure(rng.random()),
             _ => todo!(),
         }
     }
 }
 
-impl Distribution<GlycanStructure> for Standard {
+impl Distribution<GlycanStructure> for StandardUniform {
     fn sample<R: rand::prelude::Rng + ?Sized>(&self, rng: &mut R) -> GlycanStructure {
         let mut branches = Vec::new();
-        for _ in 0..rng.gen_range(0..=2) {
-            branches.push(rng.gen());
+        for _ in 0..rng.random_range(0..=2) {
+            branches.push(rng.random());
         }
-        GlycanStructure::new(rng.gen(), branches)
+        GlycanStructure::new(rng.random(), branches)
     }
 }
 
-impl Distribution<MonoSaccharide> for Standard {
+impl Distribution<MonoSaccharide> for StandardUniform {
     fn sample<R: rand::prelude::Rng + ?Sized>(&self, rng: &mut R) -> MonoSaccharide {
         let mut substituents = Vec::new();
-        for _ in 0..rng.gen_range(0..5) {
-            substituents.push(rng.gen());
+        for _ in 0..rng.random_range(0..5) {
+            substituents.push(rng.random());
         }
-        MonoSaccharide::new(rng.gen(), &substituents)
+        MonoSaccharide::new(rng.random(), &substituents)
     }
 }
 
-impl Distribution<MolecularFormula> for Standard {
+impl Distribution<MolecularFormula> for StandardUniform {
     fn sample<R: rand::prelude::Rng + ?Sized>(&self, rng: &mut R) -> MolecularFormula {
         let mut formula = MolecularFormula::default();
-        for _ in 0..rng.gen_range(0..32) {
-            let element: Element = rng.gen();
-            let isotope = rng.gen();
+        for _ in 0..rng.random_range(0..32) {
+            let element: Element = rng.random();
+            let isotope: u16 = rng.random();
+            let isotope = if rng.random::<f32>() > 0.9 {
+                None
+            } else {
+                NonZeroU16::new(isotope)
+            };
+
             if element.is_valid(isotope) {
-                let _ = formula.add((element, isotope, rng.gen()));
+                let _ = formula.add((element, isotope, rng.random()));
             }
         }
         formula
     }
 }
 
-impl Distribution<GlycanSubstituent> for Standard {
+impl Distribution<GlycanSubstituent> for StandardUniform {
     fn sample<R: rand::prelude::Rng + ?Sized>(&self, rng: &mut R) -> GlycanSubstituent {
-        match rng.gen_range(1..=44) {
+        match rng.random_range(1..=44) {
             1 => GlycanSubstituent::Acetimidoyl,
             2 => GlycanSubstituent::Acetyl,
             3 => GlycanSubstituent::AcetylAlanyl,
@@ -78,7 +91,7 @@ impl Distribution<GlycanSubstituent> for Standard {
             14 => GlycanSubstituent::DiMethyl,
             15 => GlycanSubstituent::DiMethylAcetimidoyl,
             16 => GlycanSubstituent::DiMethylGlyceryl,
-            17 => GlycanSubstituent::Element(rng.gen()),
+            17 => GlycanSubstituent::Element(rng.random()),
             18 => GlycanSubstituent::Ethanolamine,
             19 => GlycanSubstituent::EtOH,
             20 => GlycanSubstituent::Formyl,
@@ -110,9 +123,9 @@ impl Distribution<GlycanSubstituent> for Standard {
     }
 }
 
-impl Distribution<BaseSugar> for Standard {
+impl Distribution<BaseSugar> for StandardUniform {
     fn sample<R: rand::prelude::Rng + ?Sized>(&self, rng: &mut R) -> BaseSugar {
-        match rng.gen_range(0..=9) {
+        match rng.random_range(0..=9) {
             0 => BaseSugar::None,
             1 => BaseSugar::Sugar,
             2 => BaseSugar::Triose,
@@ -127,14 +140,15 @@ impl Distribution<BaseSugar> for Standard {
     }
 }
 
-impl Distribution<Element> for Standard {
+impl Distribution<Element> for StandardUniform {
     fn sample<R: rand::prelude::Rng + ?Sized>(&self, rng: &mut R) -> Element {
-        Element::try_from(rng.gen_range(Element::Electron as usize..Element::Og as usize)).unwrap()
+        Element::try_from(rng.random_range(Element::Electron as usize..Element::Og as usize))
+            .unwrap()
     }
 }
 
-impl Distribution<OrderedMass> for Standard {
+impl Distribution<OrderedMass> for StandardUniform {
     fn sample<R: rand::prelude::Rng + ?Sized>(&self, rng: &mut R) -> OrderedMass {
-        Mass::new::<dalton>(rng.gen_range(f64::MIN..f64::MAX)).into()
+        Mass::new::<dalton>(rng.random_range(f64::MIN..f64::MAX)).into()
     }
 }
diff --git a/rustyms/src/rawfile/mgf.rs b/rustyms/src/rawfile/mgf.rs
index 1fdb0526..9235c91f 100644
--- a/rustyms/src/rawfile/mgf.rs
+++ b/rustyms/src/rawfile/mgf.rs
@@ -56,7 +56,7 @@ pub fn open(path: impl AsRef<Path>) -> Result<Vec<RawSpectrum>, CustomError> {
 /// * Any line in the file could not be read
 /// * When any expected number in the file is not a number
 /// * When there is only one column (separated by space or tab) on a data row
-#[allow(clippy::missing_panics_doc)]
+#[expect(clippy::missing_panics_doc)]
 pub fn open_raw<T: std::io::Read>(reader: T) -> Result<Vec<RawSpectrum>, CustomError> {
     let reader = BufReader::new(reader);
     let mut current = RawSpectrum::default();
@@ -182,7 +182,7 @@ fn parse_charge(input: &str) -> Result<Charge, ()> {
     }
 }
 
-#[allow(clippy::missing_panics_doc)]
+#[expect(clippy::missing_panics_doc)]
 fn parse_title(title: &str, spectrum: &mut RawSpectrum) {
     // basic structure: <name>.<scan>.<scan>.<experiment?>? File:"<name>", NativeID:"(<header>) +"
     let ms_convert_format: Regex =
@@ -215,7 +215,7 @@ fn parse_title(title: &str, spectrum: &mut RawSpectrum) {
 }
 
 #[cfg(test)]
-#[allow(clippy::missing_panics_doc)]
+#[expect(clippy::missing_panics_doc)]
 mod tests {
     use super::*;
     #[test]
@@ -438,7 +438,7 @@ mod tests {
         );
     }
 
-    #[allow(clippy::type_complexity)]
+    #[expect(clippy::type_complexity)]
     fn test_title_helper(
         title: &str,
     ) -> (
diff --git a/rustyms/src/sequence_element.rs b/rustyms/src/sequence_element.rs
index d101cb57..e53ce32a 100644
--- a/rustyms/src/sequence_element.rs
+++ b/rustyms/src/sequence_element.rs
@@ -8,9 +8,9 @@ use crate::{
         CrossLinkName, LinkerSpecificity, Modification, RulePossible, SimpleModification,
         SimpleModificationInner,
     },
-    peptide::{AtLeast, Linked},
+    peptidoform::{AtLeast, Linked},
     placement_rule::PlacementRule,
-    CheckedAminoAcid, DiagnosticIon, LinearPeptide, MolecularFormula, Multi, MultiChemical,
+    CheckedAminoAcid, DiagnosticIon, MolecularFormula, Multi, MultiChemical, Peptidoform,
     SequencePosition,
 };
 use serde::{Deserialize, Serialize};
@@ -137,15 +137,14 @@ impl<T> SequenceElement<T> {
     }
 
     /// Get the molecular formulas for this position without any the ambiguous modifications
-    #[allow(clippy::filter_map_bool_then, clippy::too_many_arguments)] // has side effects
     pub(crate) fn formulas_base(
         &self,
-        all_peptides: &[LinearPeptide<Linked>],
+        all_peptides: &[Peptidoform<Linked>],
         visited_peptides: &[usize],
         applied_cross_links: &mut Vec<CrossLinkName>,
         allow_ms_cleavable: bool,
         sequence_index: SequencePosition,
-        peptide_index: usize,
+        peptidoform_index: usize,
     ) -> (Multi<MolecularFormula>, HashSet<CrossLinkName>) {
         let (formula, seen) = self
             .modifications
@@ -160,7 +159,7 @@ impl<T> SequenceElement<T> {
                         applied_cross_links,
                         allow_ms_cleavable,
                         sequence_index,
-                        peptide_index,
+                        peptidoform_index,
                     ))
                 }
             })
@@ -168,22 +167,24 @@ impl<T> SequenceElement<T> {
                 (am * m, av.union(&v).cloned().collect())
             });
         (
-            self.aminoacid.formulas_inner(sequence_index, peptide_index) * formula,
+            self.aminoacid
+                .formulas_inner(sequence_index, peptidoform_index)
+                * formula,
             seen,
         )
     }
 
     /// Get the molecular formulas for this position with the ambiguous modifications placed on the very first placed (and updating this in `placed`), without any global isotype modifications
-    #[allow(clippy::filter_map_bool_then, clippy::too_many_arguments)] // has side effects
+    #[expect(clippy::too_many_arguments)]
     pub(crate) fn formulas_greedy(
         &self,
         placed: &mut [bool],
-        all_peptides: &[LinearPeptide<Linked>],
+        all_peptides: &[Peptidoform<Linked>],
         visited_peptides: &[usize],
         applied_cross_links: &mut Vec<CrossLinkName>,
         allow_ms_cleavable: bool,
         sequence_index: SequencePosition,
-        peptide_index: usize,
+        peptidoform_index: usize,
     ) -> (Multi<MolecularFormula>, HashSet<CrossLinkName>) {
         let (formula, seen) = self
             .modifications
@@ -197,7 +198,7 @@ impl<T> SequenceElement<T> {
                         placed[*id] = true;
                         (
                             modification
-                                .formula_inner(sequence_index, peptide_index)
+                                .formula_inner(sequence_index, peptidoform_index)
                                 .into(),
                             HashSet::default(),
                         )
@@ -209,7 +210,7 @@ impl<T> SequenceElement<T> {
                         applied_cross_links,
                         allow_ms_cleavable,
                         sequence_index,
-                        peptide_index,
+                        peptidoform_index,
                     ))
                 }
             })
@@ -217,7 +218,9 @@ impl<T> SequenceElement<T> {
                 (am * m, av.union(&v).cloned().collect())
             });
         (
-            self.aminoacid.formulas_inner(sequence_index, peptide_index) * formula,
+            self.aminoacid
+                .formulas_inner(sequence_index, peptidoform_index)
+                * formula,
             seen,
         )
     }
@@ -225,12 +228,12 @@ impl<T> SequenceElement<T> {
     /// Get the molecular formulas for this position with all ambiguous modifications, without any global isotype modifications
     pub(crate) fn formulas_all(
         &self,
-        all_peptides: &[LinearPeptide<Linked>],
+        all_peptides: &[Peptidoform<Linked>],
         visited_peptides: &[usize],
         applied_cross_links: &mut Vec<CrossLinkName>,
         allow_ms_cleavable: bool,
         sequence_index: SequencePosition,
-        peptide_index: usize,
+        peptidoform_index: usize,
     ) -> (Multi<MolecularFormula>, HashSet<CrossLinkName>) {
         let (formula, seen) = self
             .modifications
@@ -242,14 +245,16 @@ impl<T> SequenceElement<T> {
                     applied_cross_links,
                     allow_ms_cleavable,
                     sequence_index,
-                    peptide_index,
+                    peptidoform_index,
                 )
             })
             .fold((Multi::default(), HashSet::new()), |(am, av), (m, v)| {
                 (am * m, av.union(&v).cloned().collect())
             });
         (
-            self.aminoacid.formulas_inner(sequence_index, peptide_index) * formula,
+            self.aminoacid
+                .formulas_inner(sequence_index, peptidoform_index)
+                * formula,
             seen,
         )
     }
diff --git a/rustyms/src/shared/aminoacid.rs b/rustyms/src/shared/aminoacid.rs
index ee2838a3..d069797d 100644
--- a/rustyms/src/shared/aminoacid.rs
+++ b/rustyms/src/shared/aminoacid.rs
@@ -2,7 +2,7 @@
 #[derive(
     Copy, Clone, Eq, PartialEq, Ord, PartialOrd, Hash, Debug, Default, Serialize, Deserialize,
 )]
-#[allow(missing_docs)]
+#[expect(missing_docs)]
 pub enum AminoAcid {
     #[default]
     Alanine = 0,
@@ -177,7 +177,7 @@ impl MultiChemical for AminoAcid {
     fn formulas_inner(
         &self,
         sequence_index: crate::SequencePosition,
-        peptide_index: usize,
+        peptidoform_index: usize,
     ) -> Multi<MolecularFormula> {
         let crate::SequencePosition::Index(sequence_index) = sequence_index else {
             panic!("Not allowed to call amino acid formulas with a terminal sequence index")
@@ -188,16 +188,16 @@ impl MultiChemical for AminoAcid {
             Self::Asparagine => molecular_formula!(H 6 C 4 O 2 N 2).into(),
             Self::AsparticAcid => molecular_formula!(H 5 C 4 O 3 N 1).into(),
             Self::AmbiguousAsparagine => vec![
-                molecular_formula!(H 6 C 4 O 2 N 2 (crate::AmbiguousLabel::AminoAcid{option: Self::Asparagine, sequence_index, peptide_index})),
-                molecular_formula!(H 5 C 4 O 3 N 1 (crate::AmbiguousLabel::AminoAcid{option: Self::AsparticAcid, sequence_index, peptide_index})),
+                molecular_formula!(H 6 C 4 O 2 N 2 (crate::AmbiguousLabel::AminoAcid{option: Self::Asparagine, sequence_index, peptidoform_index})),
+                molecular_formula!(H 5 C 4 O 3 N 1 (crate::AmbiguousLabel::AminoAcid{option: Self::AsparticAcid, sequence_index, peptidoform_index})),
             ]
             .into(),
             Self::Cysteine => molecular_formula!(H 5 C 3 O 1 N 1 S 1).into(),
             Self::Glutamine => molecular_formula!(H 8 C 5 O 2 N 2).into(),
             Self::GlutamicAcid => molecular_formula!(H 7 C 5 O 3 N 1).into(),
             Self::AmbiguousGlutamine => vec![
-                molecular_formula!(H 8 C 5 O 2 N 2 (crate::AmbiguousLabel::AminoAcid{option: Self::Glutamine, sequence_index, peptide_index})),
-                molecular_formula!(H 7 C 5 O 3 N 1 (crate::AmbiguousLabel::AminoAcid{option: Self::GlutamicAcid, sequence_index, peptide_index})),
+                molecular_formula!(H 8 C 5 O 2 N 2 (crate::AmbiguousLabel::AminoAcid{option: Self::Glutamine, sequence_index, peptidoform_index})),
+                molecular_formula!(H 7 C 5 O 3 N 1 (crate::AmbiguousLabel::AminoAcid{option: Self::GlutamicAcid, sequence_index, peptidoform_index})),
             ]
             .into(),
             Self::Glycine => molecular_formula!(H 3 C 2 O 1 N 1).into(),
diff --git a/rustyms/src/shared/element.rs b/rustyms/src/shared/element.rs
index 9d0aadb9..fb564a60 100644
--- a/rustyms/src/shared/element.rs
+++ b/rustyms/src/shared/element.rs
@@ -250,7 +250,7 @@ pub enum Element {
 
 impl TryFrom<&str> for Element {
     type Error = ();
-    #[allow(clippy::too_many_lines)]
+    #[expect(clippy::too_many_lines)]
     fn try_from(value: &str) -> Result<Self, Self::Error> {
         match value.to_ascii_lowercase().as_str() {
             "h" => Ok(Self::H),
@@ -378,7 +378,7 @@ impl TryFrom<&str> for Element {
 
 impl TryFrom<usize> for Element {
     type Error = ();
-    #[allow(clippy::too_many_lines)]
+    #[expect(clippy::too_many_lines)]
     fn try_from(value: usize) -> Result<Self, Self::Error> {
         match value {
             0 => Ok(Self::Electron),
@@ -506,7 +506,7 @@ impl TryFrom<usize> for Element {
 }
 
 impl std::fmt::Display for Element {
-    #[allow(clippy::too_many_lines)]
+    #[expect(clippy::too_many_lines)]
     fn fmt(&self, f: &mut std::fmt::Formatter<'_>) -> std::fmt::Result {
         write!(
             f,
@@ -787,6 +787,6 @@ pub const COMMON_ELEMENT_PARSE_LIST: &[(&str, Element)] = &[
     ("p", Element::P),
 ];
 
-#[allow(clippy::redundant_pub_crate)]
+#[expect(clippy::redundant_pub_crate)]
 /// The shared type to send the data from all the elements from build time to compile time
 pub(crate) type ElementalData = Vec<(Option<Mass>, Option<Mass>, Vec<(u16, Mass, f64)>)>;
diff --git a/rustyms/src/shared/formula/pro_forma.rs b/rustyms/src/shared/formula/pro_forma.rs
index be1d0c98..7fc37b0b 100644
--- a/rustyms/src/shared/formula/pro_forma.rs
+++ b/rustyms/src/shared/formula/pro_forma.rs
@@ -28,14 +28,13 @@ impl MolecularFormula {
     /// Example: [13C2]C-2H2N
     /// ```
     /// ## Allow charge
-    /// Allows electrons to be used to define the charge of the formula
+    /// Allows `:z{x}` to define the charge of a formula, eg `:z+1`, `:z-3`. As defined in ProForma 2.1.
     /// ## Allow empty
     /// Allows the string `(empty)` to be used to denote an empty formula
     /// # Errors
     /// If the formula is not valid according to the above specification, with some help on what is going wrong.
     /// # Panics
     /// It can panic if the string contains not UTF8 symbols.
-    #[allow(dead_code)]
     pub fn from_pro_forma(
         value: &str,
         range: impl RangeBounds<usize>,
@@ -44,7 +43,7 @@ impl MolecularFormula {
         allow_uncommon_elements: bool,
     ) -> Result<Self, CustomError> {
         let (mut index, end) = range.bounds(value.len().saturating_sub(1));
-        if allow_empty && value[index..=end].to_ascii_lowercase() == "(empty)" {
+        if allow_empty && value[index..=end].eq_ignore_ascii_case("(empty)") {
             return Ok(Self::default());
         }
         let mut element = None;
@@ -84,26 +83,19 @@ impl MolecularFormula {
                         .take_while(|c| c.is_ascii_alphabetic())
                         .count();
 
-                    if allow_charge
-                        && (&bytes[index + isotope + ws1..index + isotope + ws1 + ele] == b"e"
-                            || &bytes[index + isotope + ws1..index + isotope + ws1 + ele] == b"E")
-                    {
-                        element = Some(Element::Electron);
+                    for possible in if allow_uncommon_elements {
+                        ELEMENT_PARSE_LIST
                     } else {
-                        for possible in if allow_uncommon_elements {
-                            ELEMENT_PARSE_LIST
-                        } else {
-                            COMMON_ELEMENT_PARSE_LIST
-                        } {
-                            if value[index + isotope + ws1..index + isotope + ws1 + ele]
-                                .to_ascii_lowercase()
-                                == possible.0
-                            {
-                                element = Some(possible.1);
-                                break;
-                            }
+                        COMMON_ELEMENT_PARSE_LIST
+                    } {
+                        if value[index + isotope + ws1..index + isotope + ws1 + ele]
+                            .to_ascii_lowercase()
+                            == possible.0
+                        {
+                            element = Some(possible.1);
+                            break;
                         }
-                    };
+                    }
                     if let Some(parsed_element) = element {
                         let ws2 = bytes[index + isotope + ws1 + ele..]
                             .iter()
@@ -198,6 +190,25 @@ impl MolecularFormula {
                     index += len;
                 }
                 b' ' => index += 1,
+                b':' if allow_charge => {
+                    if Some(&b'z') == bytes.get(index + 1) {
+                        index += 2;
+                        let num = value[index..=end].parse::<i32>().map_err(|err| {
+                            CustomError::error(
+                                "Invalid ProForma molecular formula",
+                                format!("The charge number is {}", explain_number_error(&err)),
+                                Context::line(None, value, index, end - index),
+                            )
+                        })?;
+                        let _ = result.add((Element::Electron, None, -num));
+                        break 'main_parse_loop;
+                    }
+                    return Err(CustomError::error(
+                        "Invalid ProForma molecular formula",
+                            "A charge tag was not set up properly, a charge tag should be formed as ':z<sign><number>'",
+                        Context::line(None, value, index - 1, if bytes.len() < index {1} else {2}),
+                    ));
+                }
                 _ => {
                     if let Some(element) = element {
                         if !Self::add(&mut result, (element, None, 1)) {
@@ -224,11 +235,6 @@ impl MolecularFormula {
                             continue 'main_parse_loop;
                         }
                     }
-                    if allow_charge && (bytes[index] == b'e' || bytes[index] == b'E') {
-                        element = Some(Element::Electron);
-                        index += 1;
-                        continue 'main_parse_loop;
-                    }
                     return Err(CustomError::error(
                         "Invalid ProForma molecular formula",
                         "Not a valid character in formula",
diff --git a/rustyms/src/shared/formula/structure.rs b/rustyms/src/shared/formula/structure.rs
index 12d487d8..6b12204c 100644
--- a/rustyms/src/shared/formula/structure.rs
+++ b/rustyms/src/shared/formula/structure.rs
@@ -8,6 +8,7 @@ use std::{
     num::NonZeroU16,
     ops::{Add, AddAssign, Mul, Neg, Sub},
 };
+use thin_vec::ThinVec;
 
 /// A molecular formula, a selection of elements of specified isotopes together forming a structure
 #[allow(clippy::unsafe_derive_deserialize)]
@@ -15,12 +16,12 @@ use std::{
 pub struct MolecularFormula {
     /// Save all constituent parts as the element in question, the isotope (or None for natural distribution), and the number of this part
     /// The elements will be sorted on element/isotope and deduplicated, guaranteed to only contain valid isotopes.
-    pub(in super::super) elements: Vec<(crate::Element, Option<NonZeroU16>, i32)>,
+    pub(in super::super) elements: ThinVec<(crate::Element, Option<NonZeroU16>, i32)>,
     /// Any addition mass, defined to be monoisotopic
     pub(in super::super) additional_mass: OrderedFloat<f64>,
     /// The labels of sources of ambiguity/multiplicity
     #[serde(default)]
-    pub(in super::super) labels: Vec<AmbiguousLabel>,
+    pub(in super::super) labels: ThinVec<AmbiguousLabel>,
 }
 
 /// Keep track of what ambiguous option is used
@@ -33,7 +34,7 @@ pub enum AmbiguousLabel {
         /// What location in the sequence are we talking about
         sequence_index: usize,
         /// Peptide index
-        peptide_index: usize,
+        peptidoform_index: usize,
     },
     /// A ambiguous modification, with the actual position
     Modification {
@@ -42,7 +43,7 @@ pub enum AmbiguousLabel {
         /// Which location
         sequence_index: SequencePosition,
         /// Peptide index
-        peptide_index: usize,
+        peptidoform_index: usize,
     },
     /// The actual charge used, when there are multiple charge carriers
     ChargeCarrier(MolecularFormula),
@@ -53,9 +54,9 @@ pub enum AmbiguousLabel {
 }
 
 /// Any item that has a clearly defined single molecular formula
-#[allow(dead_code)]
 pub trait Chemical {
     /// Get the molecular formula
+    #[allow(dead_code)]
     fn formula(&self) -> MolecularFormula {
         self.formula_inner(SequencePosition::default(), 0)
     }
@@ -64,7 +65,7 @@ pub trait Chemical {
     fn formula_inner(
         &self,
         sequence_index: SequencePosition,
-        peptide_index: usize,
+        peptidoform_index: usize,
     ) -> MolecularFormula;
 }
 
@@ -72,10 +73,10 @@ impl<T: Chemical> Chemical for &[T] {
     fn formula_inner(
         &self,
         sequence_index: SequencePosition,
-        peptide_index: usize,
+        peptidoform_index: usize,
     ) -> MolecularFormula {
         self.iter()
-            .map(|f| f.formula_inner(sequence_index, peptide_index))
+            .map(|f| f.formula_inner(sequence_index, peptidoform_index))
             .sum()
     }
 }
@@ -84,16 +85,15 @@ impl<T: Chemical> Chemical for &Vec<T> {
     fn formula_inner(
         &self,
         sequence_index: SequencePosition,
-        peptide_index: usize,
+        peptidoform_index: usize,
     ) -> MolecularFormula {
         self.iter()
-            .map(|f| f.formula_inner(sequence_index, peptide_index))
+            .map(|f| f.formula_inner(sequence_index, peptidoform_index))
             .sum()
     }
 }
 
 /// Any item that has a number of potential chemical formulas
-#[allow(dead_code)]
 pub trait MultiChemical {
     /// Get all possible molecular formulas
     fn formulas(&self) -> Multi<MolecularFormula> {
@@ -104,7 +104,7 @@ pub trait MultiChemical {
     fn formulas_inner(
         &self,
         sequence_index: SequencePosition,
-        peptide_index: usize,
+        peptidoform_index: usize,
     ) -> Multi<MolecularFormula>;
 
     /// Get the charge of this chemical, it returns None if no charge is defined.
@@ -123,12 +123,13 @@ pub trait MultiChemical {
     }
 
     /// Return a single formula if this `MultiChemical` has only one possible formula while keeping track of all ambiguous labels
+    #[allow(dead_code)]
     fn single_formula_inner(
         &self,
         sequence_index: SequencePosition,
-        peptide_index: usize,
+        peptidoform_index: usize,
     ) -> Option<MolecularFormula> {
-        let formulas = self.formulas_inner(sequence_index, peptide_index);
+        let formulas = self.formulas_inner(sequence_index, peptidoform_index);
         (formulas.len() == 1).then_some(formulas.to_vec().pop().unwrap())
     }
 }
@@ -143,9 +144,9 @@ impl MolecularFormula {
             None
         } else {
             let result = Self {
-                elements: elements.to_vec(),
+                elements: elements.into(),
                 additional_mass: 0.0.into(),
-                labels: labels.to_vec(),
+                labels: labels.into(),
             };
             Some(result.simplify())
         }
@@ -177,28 +178,27 @@ impl MolecularFormula {
                 index += 1;
             }
         }
-        self.elements.retain(|el| el.2 != 0);
+        self.elements
+            .retain(|el: &(Element, Option<std::num::NonZero<u16>>, i32)| el.2 != 0);
         self
     }
 
     /// Get an empty molecular formula with only a mass of unspecified origin
-    pub const fn with_additional_mass(additional_mass: f64) -> Self {
+    pub fn with_additional_mass(additional_mass: f64) -> Self {
         Self {
-            elements: Vec::new(),
+            elements: ThinVec::new(),
             additional_mass: OrderedFloat(additional_mass),
-            labels: Vec::new(),
+            labels: ThinVec::new(),
         }
     }
 
     /// Add the following labels to this formula
-    #[allow(dead_code)]
     pub(crate) fn with_labels(mut self, labels: &[AmbiguousLabel]) -> Self {
         self.labels.extend_from_slice(labels);
         self
     }
 
     /// Add the following label to this formula
-    #[allow(dead_code)]
     pub(crate) fn with_label(mut self, label: AmbiguousLabel) -> Self {
         self.labels.push(label);
         self
@@ -328,18 +328,17 @@ impl MolecularFormula {
                     f(hydrogen, &mut buffer);
                 }
             }
-            for element in self
-                .elements
-                .iter()
-                .filter(|e| !((e.0 == Element::H || e.0 == Element::C) && e.1.is_none()))
-            {
+            for element in self.elements.iter().filter(|e| {
+                !((e.0 == Element::H || e.0 == Element::C || e.0 == Element::Electron)
+                    && e.1.is_none())
+            }) {
                 if element.2 != 0 {
                     f(element, &mut buffer);
                 }
             }
         } else {
             for element in &self.elements {
-                if element.2 != 0 {
+                if element.2 != 0 && element.0 != Element::Electron {
                     f(element, &mut buffer);
                 }
             }
@@ -347,6 +346,9 @@ impl MolecularFormula {
         if self.additional_mass != 0.0 {
             write!(&mut buffer, "{:+}", self.additional_mass).unwrap();
         }
+        if self.charge().value != 0 {
+            write!(&mut buffer, ":z{:+}", self.charge().value).unwrap();
+        }
         buffer
     }
 }
diff --git a/rustyms/src/shared/glycan.rs b/rustyms/src/shared/glycan.rs
index b5b7b8a5..96e1dec4 100644
--- a/rustyms/src/shared/glycan.rs
+++ b/rustyms/src/shared/glycan.rs
@@ -122,8 +122,8 @@ impl MonoSaccharide {
         // Prefix mods
         let mut amount = 1;
         if bytes[index].is_ascii_digit() {
-            match bytes[index + 1] {
-                b',' if bytes[index + 3] == b':' => {
+            match bytes.get(index + 1) {
+                Some(b',') if bytes.get(index + 3).copied() == Some(b':') => {
                     let start_index = index;
                     index += 7;
                     index += line[index..].ignore(&["-"]);
@@ -146,7 +146,7 @@ impl MonoSaccharide {
                         GlycanSubstituent::Deoxy,
                     ]);
                 }
-                b',' => {
+                Some(b',') => {
                     let num = bytes[index + 1..]
                         .iter()
                         .take_while(|c| c.is_ascii_digit() || **c == b',' || **c == b'?')
@@ -155,7 +155,8 @@ impl MonoSaccharide {
                     amount = num / 2;
                     // X,X{mod} (or 3/4/5/etc mods)
                 }
-                _ => index += 1, // X{mod}
+                Some(_) => index += 1, // X{mod}
+                None => (),
             }
             index += line[index..].ignore(&["-"]);
         }
@@ -405,13 +406,14 @@ impl Chemical for MonoSaccharide {
     fn formula_inner(
         &self,
         sequence_index: SequencePosition,
-        peptide_index: usize,
+        peptidoform_index: usize,
     ) -> MolecularFormula {
-        self.base_sugar.formula_inner(sequence_index, peptide_index)
+        self.base_sugar
+            .formula_inner(sequence_index, peptidoform_index)
             + self
                 .substituents
                 .as_slice()
-                .formula_inner(sequence_index, peptide_index)
+                .formula_inner(sequence_index, peptidoform_index)
     }
 }
 
@@ -483,7 +485,7 @@ impl Chemical for BaseSugar {
     fn formula_inner(
         &self,
         _sequence_index: SequencePosition,
-        _peptide_index: usize,
+        _peptidoform_index: usize,
     ) -> MolecularFormula {
         match self {
             Self::None => MolecularFormula::default(),
@@ -720,7 +722,7 @@ impl Chemical for GlycanSubstituent {
     fn formula_inner(
         &self,
         _sequence_index: SequencePosition,
-        _peptide_index: usize,
+        _peptidoform_index: usize,
     ) -> MolecularFormula {
         let side = match self {
             Self::Acetimidoyl => molecular_formula!(H 5 C 2 N 1),
diff --git a/rustyms/src/shared/glycan_structure.rs b/rustyms/src/shared/glycan_structure.rs
index 5fafce95..3159e567 100644
--- a/rustyms/src/shared/glycan_structure.rs
+++ b/rustyms/src/shared/glycan_structure.rs
@@ -154,13 +154,13 @@ impl Chemical for GlycanStructure {
     fn formula_inner(
         &self,
         sequence_index: crate::SequencePosition,
-        peptide_index: usize,
+        peptidoform_index: usize,
     ) -> MolecularFormula {
-        self.sugar.formula_inner(sequence_index, peptide_index)
+        self.sugar.formula_inner(sequence_index, peptidoform_index)
             + self
                 .branches
                 .iter()
-                .map(|f| f.formula_inner(sequence_index, peptide_index))
+                .map(|f| f.formula_inner(sequence_index, peptidoform_index))
                 .sum::<MolecularFormula>()
     }
 }
diff --git a/rustyms/src/shared/modification.rs b/rustyms/src/shared/modification.rs
index 75cc2caa..9a59228e 100644
--- a/rustyms/src/shared/modification.rs
+++ b/rustyms/src/shared/modification.rs
@@ -31,7 +31,9 @@ pub enum Modification {
     },
 }
 
-/// Indicate the cross-link side
+/// Indicate the cross-link side, it contains a set of all placement rules that apply for the placed
+/// location to find all possible ways of breaking and/or neutral losses. These numbers are the
+/// index into the [`LinkerSpecificity`] rules.
 #[derive(Clone, PartialEq, Eq, Debug, Serialize, Deserialize)]
 pub enum CrossLinkSide {
     /// The cross-link is symmetric, or if asymmetric it can be placed in both orientations
@@ -90,7 +92,6 @@ pub enum SimpleModificationInner {
     /// A modification defined with a monoisotopic mass shift
     Mass(OrderedMass),
     /// A modification defined with a molecular formula
-    #[allow(non_snake_case)]
     Formula(MolecularFormula),
     /// A glycan without a defined structure
     Glycan(Vec<(MonoSaccharide, isize)>),
diff --git a/rustyms/src/shared/multi.rs b/rustyms/src/shared/multi.rs
index 75815668..6e9381c9 100644
--- a/rustyms/src/shared/multi.rs
+++ b/rustyms/src/shared/multi.rs
@@ -99,9 +99,9 @@ where
     }
 }
 
-impl<'a, M> Add<M> for Multi<M>
+impl<M> Add<M> for Multi<M>
 where
-    M: Add<M, Output = M> + Clone + 'a,
+    M: Add<M, Output = M> + Clone,
 {
     type Output = Self;
     /// Adds this formula to all formulas in the multi formula
@@ -145,9 +145,9 @@ where
     }
 }
 
-impl<'a, M> Sub<M> for Multi<M>
+impl<M> Sub<M> for Multi<M>
 where
-    M: Sub<M, Output = M> + Clone + 'a,
+    M: Sub<M, Output = M> + Clone,
 {
     type Output = Self;
     /// Subtracts this formula from all formulas in the multi formula
@@ -173,7 +173,7 @@ where
     }
 }
 
-impl<'a, M> Mul<&'a Self> for Multi<M>
+impl<M> Mul<&Self> for Multi<M>
 where
     M: Add<M, Output = M> + Clone,
 {
@@ -235,9 +235,9 @@ where
     }
 }
 
-impl<'a, M> MulAssign<Self> for Multi<M>
+impl<M> MulAssign<Self> for Multi<M>
 where
-    M: Add<M, Output = M> + 'a + Clone,
+    M: Add<M, Output = M> + Clone,
 {
     fn mul_assign(&mut self, rhs: Self) {
         let new_data = self
@@ -314,7 +314,7 @@ impl<'a, M: Clone + 'a> std::iter::FromIterator<&'a M> for Multi<M> {
     }
 }
 
-#[allow(dead_code)]
+#[expect(dead_code)]
 impl crate::Multi<crate::MolecularFormula> {
     pub(crate) fn with_labels(self, labels: &[crate::AmbiguousLabel]) -> Self {
         Self(
diff --git a/rustyms/src/shared/sequence_position.rs b/rustyms/src/shared/sequence_position.rs
index d2f4bdec..446bbb48 100644
--- a/rustyms/src/shared/sequence_position.rs
+++ b/rustyms/src/shared/sequence_position.rs
@@ -29,7 +29,8 @@ impl std::fmt::Display for SequencePosition {
 
 impl SequencePosition {
     /// Reverse this position, if the peptide would be reversed what would this location be in that reversed peptide.
-    pub fn reverse(self, peptide_length: usize) -> Self {
+    #[must_use]
+    pub const fn reverse(self, peptide_length: usize) -> Self {
         match self {
             Self::NTerm => Self::CTerm,
             Self::Index(i) => Self::Index(peptide_length - i),
diff --git a/rustyms/src/spectrum/annotated.rs b/rustyms/src/spectrum/annotated.rs
index 867182f9..6b3a0dc7 100644
--- a/rustyms/src/spectrum/annotated.rs
+++ b/rustyms/src/spectrum/annotated.rs
@@ -11,7 +11,7 @@ use crate::{
         f64::{Mass, MassOverCharge, Time},
         usize::Charge,
     },
-    CompoundPeptidoform,
+    CompoundPeptidoformIon,
 };
 
 use super::{PeakSpectrum, RawPeak};
@@ -30,7 +30,7 @@ pub struct AnnotatedSpectrum {
     /// The found precursor mass
     pub mass: Option<Mass>,
     /// The peptide with which this spectrum was annotated
-    pub peptide: CompoundPeptidoform,
+    pub peptide: CompoundPeptidoformIon,
     /// The spectrum
     pub(super) spectrum: Vec<AnnotatedPeak>,
 }
diff --git a/rustyms/src/spectrum/fdr.rs b/rustyms/src/spectrum/fdr.rs
index d5ae85a9..68744dca 100644
--- a/rustyms/src/spectrum/fdr.rs
+++ b/rustyms/src/spectrum/fdr.rs
@@ -27,27 +27,28 @@ impl AnnotatedSpectrum {
             .iter()
             .filter_map(|f| {
                 f.mz(mass_mode)
-                    .map(|mz| (mz, f.peptidoform_index, f.peptide_index))
+                    .map(|mz| (mz, f.peptidoform_ion_index, f.peptidoform_index))
             })
             .filter(|(mz, _, _)| model.mz_range.contains(mz))
             .collect_vec();
 
         let individual_peptides = self
             .peptide
-            .peptidoforms()
+            .peptidoform_ions()
             .iter()
             .enumerate()
-            .map(|(peptidoform_index, peptidoform)| {
+            .map(|(peptidoform_ion_index, peptidoform)| {
                 peptidoform
-                    .peptides()
+                    .peptidoforms()
                     .iter()
                     .enumerate()
-                    .map(|(peptide_index, _)| {
+                    .map(|(peptidoform_index, _)| {
                         self.internal_fdr(
                             mzs.iter()
                                 .filter_map(|(mz, pi, ppi)| {
-                                    (*pi == Some(peptidoform_index) && *ppi == Some(peptide_index))
-                                        .then_some(*mz)
+                                    (*pi == Some(peptidoform_ion_index)
+                                        && *ppi == Some(peptidoform_index))
+                                    .then_some(*mz)
                                 })
                                 .collect_vec()
                                 .as_slice(),
@@ -92,7 +93,7 @@ impl AnnotatedSpectrum {
 
                 // Check index-1, index and index+1 (if existing) to find the one with the lowest ppm
                 let mut closest = (0, Ratio::new::<crate::system::ratio::ppm>(f64::INFINITY));
-                #[allow(clippy::needless_range_loop)] // I like this better
+                #[expect(clippy::needless_range_loop)] // I like this better
                 for i in if index == 0 { 0 } else { index - 1 }
                     ..=(index + 1).min(self.spectrum.len().saturating_sub(1))
                 {
diff --git a/rustyms/src/spectrum/fragmentation.rs b/rustyms/src/spectrum/fragmentation.rs
index 43c4a2a3..2f5c052c 100644
--- a/rustyms/src/spectrum/fragmentation.rs
+++ b/rustyms/src/spectrum/fragmentation.rs
@@ -1,4 +1,4 @@
-use crate::{system::MassOverCharge, CompoundPeptidoform, Fragment, MassMode, Model};
+use crate::{system::MassOverCharge, CompoundPeptidoformIon, Fragment, MassMode, Model};
 
 use super::AnnotatedSpectrum;
 
@@ -14,7 +14,7 @@ pub trait AnnotatableSpectrum {
 
     /// Create an empty annotated spectrum, which is required to fill the spectrum vector with
     /// [`blank`](crate::spectrum::AnnotatedPeak::background) annotated peaks.
-    fn empty_annotated(&self, peptide: CompoundPeptidoform) -> AnnotatedSpectrum;
+    fn empty_annotated(&self, peptide: CompoundPeptidoformIon) -> AnnotatedSpectrum;
 
     /// Search for a specific mz within the tolerance. Has to return the index in the annotated
     /// spectrum vector for closest peak (if there is any).
@@ -24,7 +24,7 @@ pub trait AnnotatableSpectrum {
     /// [`crate::CompoundPeptidoform::generate_theoretical_fragments`].
     fn annotate(
         &self,
-        peptide: CompoundPeptidoform,
+        peptide: CompoundPeptidoformIon,
         theoretical_fragments: &[Fragment],
         model: &Model,
         mode: MassMode,
diff --git a/rustyms/src/spectrum/mzdata.rs b/rustyms/src/spectrum/mzdata.rs
index 70f2692f..5cd71303 100644
--- a/rustyms/src/spectrum/mzdata.rs
+++ b/rustyms/src/spectrum/mzdata.rs
@@ -3,13 +3,13 @@ use mzdata::{prelude::*, spectrum::RefPeakDataLevel};
 use crate::{
     spectrum::{AnnotatableSpectrum, AnnotatedPeak, AnnotatedSpectrum},
     system::MassOverCharge,
-    CompoundPeptidoform,
+    CompoundPeptidoformIon,
 };
 
 impl<S: SpectrumLike> AnnotatableSpectrum for S {
     type Tolerance = Tolerance;
 
-    fn empty_annotated(&self, peptide: CompoundPeptidoform) -> AnnotatedSpectrum {
+    fn empty_annotated(&self, peptide: CompoundPeptidoformIon) -> AnnotatedSpectrum {
         AnnotatedSpectrum {
             title: self.description().id.clone(),
             num_scans: self.description().acquisition.scans.len() as u64,
diff --git a/rustyms/src/spectrum/raw.rs b/rustyms/src/spectrum/raw.rs
index f69b1bf5..cd828b7c 100644
--- a/rustyms/src/spectrum/raw.rs
+++ b/rustyms/src/spectrum/raw.rs
@@ -12,7 +12,7 @@ use crate::{
         f64::{Mass, MassOverCharge, Ratio, Time},
         usize::Charge,
     },
-    AnnotatedSpectrum, CompoundPeptidoform, Tolerance, WithinTolerance,
+    AnnotatedSpectrum, CompoundPeptidoformIon, Tolerance, WithinTolerance,
 };
 
 /// A raw spectrum (meaning not annotated yet)
@@ -78,7 +78,7 @@ impl RawSpectrum {
     }
 
     /// Filter a spectrum by dividing it in windows and within each window only retain the `top` number of peaks.
-    #[allow(clippy::missing_panics_doc)] // Cannot panic as it checks with peek first
+    #[expect(clippy::missing_panics_doc)] // Cannot panic as it checks with peek first
     pub fn top_x_filter(&mut self, window_size: f64, top: usize) {
         let mut new_spectrum = Vec::with_capacity(
             self.spectrum
@@ -116,7 +116,7 @@ impl RawSpectrum {
 impl AnnotatableSpectrum for RawSpectrum {
     type Tolerance = Tolerance<MassOverCharge>;
 
-    fn empty_annotated(&self, peptide: CompoundPeptidoform) -> AnnotatedSpectrum {
+    fn empty_annotated(&self, peptide: CompoundPeptidoformIon) -> AnnotatedSpectrum {
         AnnotatedSpectrum {
             title: self.title.clone(),
             num_scans: self.num_scans,
diff --git a/rustyms/src/spectrum/scores.rs b/rustyms/src/spectrum/scores.rs
index c93f30d6..f43253f9 100644
--- a/rustyms/src/spectrum/scores.rs
+++ b/rustyms/src/spectrum/scores.rs
@@ -5,8 +5,8 @@ use serde::{Deserialize, Serialize};
 
 use crate::{
     fragment::{Fragment, FragmentKind},
-    peptide::UnAmbiguous,
-    AnnotatedSpectrum, LinearPeptide, MassMode, Model,
+    peptidoform::UnAmbiguous,
+    AnnotatedSpectrum, MassMode, Model, Peptidoform,
 };
 
 impl AnnotatedSpectrum {
@@ -29,26 +29,26 @@ impl AnnotatedSpectrum {
         let total_intensity: f64 = self.spectrum.iter().map(|p| *p.intensity).sum();
         let individual_peptides = self
             .peptide
-            .peptidoforms()
+            .peptidoform_ions()
             .iter()
             .enumerate()
-            .map(|(peptidoform_index, peptidoform)| {
+            .map(|(peptidoform_ion_index, peptidoform)| {
                 peptidoform
-                    .peptides()
+                    .peptidoforms()
                     .iter()
                     .enumerate()
-                    .map(|(peptide_index, peptide)| {
+                    .map(|(peptidoform_index, peptide)| {
                         let (recovered_fragments, peaks, intensity_annotated) = self
                             .filtered_base_score(
                                 &fragments,
+                                Some(peptidoform_ion_index),
                                 Some(peptidoform_index),
-                                Some(peptide_index),
                                 None,
                             );
                         let (positions, expected_positions) = self.score_positions(
                             &fragments,
+                            peptidoform_ion_index,
                             peptidoform_index,
-                            peptide_index,
                             None,
                         );
                         Scores {
@@ -64,7 +64,7 @@ impl AnnotatedSpectrum {
                             },
                             ions: self.score_individual_ions(
                                 &fragments,
-                                Some((peptidoform_index, peptide_index, peptide)),
+                                Some((peptidoform_ion_index, peptidoform_index, peptide)),
                                 total_intensity,
                             ),
                         }
@@ -95,8 +95,8 @@ impl AnnotatedSpectrum {
     fn filtered_base_score(
         &self,
         fragments: &[&Fragment],
+        peptidoform_ion_index: Option<usize>,
         peptidoform_index: Option<usize>,
-        peptide_index: Option<usize>,
         ion: Option<FragmentKind>,
     ) -> (Recovered<u32>, Recovered<u32>, f64) {
         let (peaks_annotated, fragments_found, intensity_annotated) = self
@@ -107,8 +107,8 @@ impl AnnotatedSpectrum {
                     .annotation
                     .iter()
                     .filter(|a| {
-                        peptidoform_index.map_or(true, |i| a.peptidoform_index == Some(i))
-                            && peptide_index.map_or(true, |i| a.peptide_index == Some(i))
+                        peptidoform_ion_index.map_or(true, |i| a.peptidoform_ion_index == Some(i))
+                            && peptidoform_index.map_or(true, |i| a.peptidoform_index == Some(i))
                             && ion.map_or(true, |kind| a.ion.kind() == kind)
                     })
                     .count() as u32;
@@ -124,8 +124,8 @@ impl AnnotatedSpectrum {
         let total_fragments = fragments
             .iter()
             .filter(|f| {
-                peptidoform_index.map_or(true, |i| f.peptidoform_index == Some(i))
-                    && peptide_index.map_or(true, |i| f.peptide_index == Some(i))
+                peptidoform_ion_index.map_or(true, |i| f.peptidoform_ion_index == Some(i))
+                    && peptidoform_index.map_or(true, |i| f.peptidoform_index == Some(i))
                     && ion.map_or(true, |kind| f.ion.kind() == kind)
             })
             .count() as u32;
@@ -140,8 +140,8 @@ impl AnnotatedSpectrum {
     fn score_positions(
         &self,
         fragments: &[&Fragment],
+        peptidoform_ion_index: usize,
         peptidoform_index: usize,
-        peptide_index: usize,
         ion: Option<FragmentKind>,
     ) -> (u32, u32) {
         (
@@ -151,8 +151,8 @@ impl AnnotatedSpectrum {
                     p.annotation
                         .iter()
                         .filter(|a| {
-                            a.peptidoform_index == Some(peptidoform_index)
-                                && a.peptide_index == Some(peptide_index)
+                            a.peptidoform_ion_index == Some(peptidoform_ion_index)
+                                && a.peptidoform_index == Some(peptidoform_index)
                                 && ion.map_or(true, |kind| a.ion.kind() == kind)
                         })
                         .filter_map(|a| a.ion.position())
@@ -163,8 +163,8 @@ impl AnnotatedSpectrum {
             fragments
                 .iter()
                 .filter(|f| {
-                    f.peptidoform_index == Some(peptidoform_index)
-                        && f.peptide_index == Some(peptide_index)
+                    f.peptidoform_ion_index == Some(peptidoform_ion_index)
+                        && f.peptidoform_index == Some(peptidoform_index)
                         && ion.map_or(true, |i| i == f.ion.kind())
                 })
                 .filter_map(|f| f.ion.position().map(|p| p.sequence_index))
@@ -177,7 +177,7 @@ impl AnnotatedSpectrum {
     fn score_unique_formulas(
         &self,
         fragments: &[&Fragment],
-        peptide_index: Option<usize>,
+        peptidoform_index: Option<usize>,
         ion: Option<FragmentKind>,
     ) -> Recovered<u32> {
         let num_annotated = self
@@ -185,7 +185,7 @@ impl AnnotatedSpectrum {
             .iter()
             .flat_map(|p| {
                 p.annotation.iter().filter(|a| {
-                    peptide_index.map_or(true, |i| a.peptide_index == Some(i))
+                    peptidoform_index.map_or(true, |i| a.peptidoform_index == Some(i))
                         && ion.map_or(true, |kind| a.ion.kind() == kind)
                 })
             })
@@ -195,7 +195,7 @@ impl AnnotatedSpectrum {
         let total_fragments = fragments
             .iter()
             .filter(|f| {
-                peptide_index.map_or(true, |i| f.peptide_index == Some(i))
+                peptidoform_index.map_or(true, |i| f.peptidoform_index == Some(i))
                     && ion.map_or(true, |kind| f.ion.kind() == kind)
             })
             .map(|f| f.formula.clone())
@@ -208,7 +208,7 @@ impl AnnotatedSpectrum {
     fn score_individual_ions<T>(
         &self,
         fragments: &[&Fragment],
-        peptide: Option<(usize, usize, &LinearPeptide<T>)>,
+        peptide: Option<(usize, usize, &Peptidoform<T>)>,
         total_intensity: f64,
     ) -> Vec<(FragmentKind, Score)> {
         [
@@ -231,12 +231,12 @@ impl AnnotatedSpectrum {
                 peptide.as_ref().map(|p| p.1),
                 Some(ion),
             );
-            if let Some((peptidoform_index, peptide_index, peptide)) = peptide {
+            if let Some((peptidoform_ion_index, peptidoform_index, peptide)) = peptide {
                 if recovered_fragments.total > 0 {
                     let (positions, expected_positions) = self.score_positions(
                         fragments,
+                        peptidoform_ion_index,
                         peptidoform_index,
-                        peptide_index,
                         Some(ion),
                     );
                     Some((
diff --git a/rustyms/src/system.rs b/rustyms/src/system.rs
index 5e9adfcc..2b8e06b7 100644
--- a/rustyms/src/system.rs
+++ b/rustyms/src/system.rs
@@ -143,7 +143,6 @@ pub mod f64 {
     pub use super::time::s;
 
     /// Annotate the given number as being in Da
-    #[allow(dead_code)]
     pub fn da(v: f64) -> Mass {
         Mass::new::<super::mass::dalton>(v)
     }
@@ -200,6 +199,11 @@ impl MassOverCharge {
     pub fn ppm(self, b: Self) -> Ratio {
         Ratio::new::<crate::system::ratio::ppm>(((self - b).abs() / self.abs()).value * 1e6)
     }
+
+    /// Signed ppm error between this mz and the given other
+    pub fn signed_ppm(self, b: Self) -> Ratio {
+        Ratio::new::<crate::system::ratio::ppm>(((self - b) / self).value * 1e6)
+    }
 }
 
 impl Mass {
@@ -207,6 +211,11 @@ impl Mass {
     pub fn ppm(self, b: Self) -> Ratio {
         Ratio::new::<crate::system::ratio::ppm>(((self - b).abs() / self.abs()).value * 1e6)
     }
+
+    /// Signed ppm error between this mass and the given other
+    pub fn signed_ppm(self, b: Self) -> Ratio {
+        Ratio::new::<crate::system::ratio::ppm>(((self - b) / self).value * 1e6)
+    }
 }
 
 /// A wrapper around [`Ratio`] which implements Eq/Ord/Hash to help in auto deriving these on other structs.